SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9510996 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017319 | AGTGAGTGGTGGACC[C/G]GAACCAGAACCTACG | 221178 |
rs9510997 | snp | G/T | 0.363568 | 0.222716 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018718 | TTTCATTTGCTATTT[G/T]TCCTGTGTTTTACTT | 221178 |
rs9510998 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024688 | ATTTGATGACATAAA[A/T]ATATATTTGCCTgcc | 221178 |
rs9511000 | snp | C/G | 0.49975 | 0.0111793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025873 | ggagtgcaatggcgc[C/G]atctcactacaacct | 221178 |
rs9511001 | snp | A/G | 0.133777 | 0.221342 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026541 | CAAAATTGTATGTAG[A/G]AATTGGATACAAACT | 221178 |
rs9511002 | snp | G/T | 0.469247 | 0.120128 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026740 | CCGCCACCACGTCCA[G/T]CTAATTTTTTGTATT | 221178 |
rs9511003 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026812 | TGGATCTCCTGACCT[C/T]GTGATCCGCCCTTGT | 221178 |
rs9511006 | snp | A/G | 0.137187 | 0.223099 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034210 | GCAAGAAGGGAACTC[A/G]AGTAGGAAAGTCAGC | 221178 |
rs9511007 | snp | C/T | 0.336245 | 0.234652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037794 | TCGTGGATTAGCTTA[C/T]TGGGGGCCCATGAAA | 221178 |
rs9511008 | snp | C/T | 0.464416 | 0.128553 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038146 | TCTCGATCTCCTGAC[C/T]TCGTGATCCGCCTGC | 221178 |
rs9511009 | snp | C/T | 0.498133 | 0.030494 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042415 | GGCCGCTTTCTGAGA[C/T]GTTGCGTGTTCACAG | 221178 |
rs9511010 | snp | C/T | 0.124144 | 0.21601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042568 | ACACAAGCGCACATC[C/T]ATGCCCGTGCGCGAA | 221178 |
rs9511011 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042666 | CTGAACTAACTCAAA[A/G]GGGAGAGCTTCTCAA | 221178 |
rs9511013 | snp | A/G | 0.498059 | 0.0310896 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043144 | AGGAACATCAGCAGC[A/G]GGTGGCCTCGGTGTT | 221178 |
rs9511014 | snp | C/G | 0.498059 | 0.0310896 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043153 | AGCAGCGGGTGGCCT[C/G]GGTGTTCTCCGCACC | 221178 |
rs9511015 | snp | A/G | 0.498182 | 0.0300969 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043890 | ATAAGGACTGCCAGG[A/G]GAGGGGTAGGTGGCA | 221178 |
rs9511016 | snp | G/T | 0.498182 | 0.0300969 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043894 | GGACTGCCAGGGGAG[G/T]GGTAGGTGGCAACTT | 221178 |
rs9511017 | snp | A/C | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046855 | accagatccttcttg[A/C]ccactgcagagataa | 221178 |
rs9511020 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051273 | AAGTGATTTCCAATC[A/G]CGTTGGACATGCTGT | 221178 |
rs9511021 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053180 | CAAGAACATTTTTGT[G/T]TACTTGCATTTTATA | 221178 |
rs9511022 | snp | G/T | 0.119281 | 0.213102 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053269 | GGATTCGGCCTCAGT[G/T]CTGTGATCCACAAAG | 221178 |
rs9511023 | snp | A/G | 0.478104 | 0.102316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057657 | ACCTCCAACCGTCAT[A/G]AGAAATGTTACTTCC | 221178 |
rs9511024 | snp | C/G | 0.488905 | 0.0736498 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059532 | TCTGAGGTGGAATCC[C/G]CAAAGGAGGAAGACA | 221178 |
rs9511025 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059698 | tcttgcacactgatt[C/T]tgtatgctggaactt | 221178 |
rs9511026 | snp | A/G | 0.488905 | 0.0736498 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061022 | ccagctggggcaaca[A/G]agcaagactctgccc | 221178 |
rs9511027 | snp | A/G | 0.497091 | 0.0380279 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061089 | acacttttcaaaaga[A/G]gacatacatgtggct | 221178 |
rs9511031 | snp | A/G | 0.491104 | 0.0660973 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067459 | AAGAACTACTTTTCC[A/G]TCAAATACCAAGCCC | 221178 |
rs9511032 | snp | A/G | 0.491421 | 0.0649309 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067541 | TAAATTCACAGTGAT[A/G]GAGCTGTAATAAATA | 221178 |
rs9511033 | snp | G/T | 0.345037 | 0.231231 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071952 | GCTGGTTATGGCAAG[G/T]TATTGGTGGTGGTGT | 221178 |
rs9511035 | snp | C/T | 0.25801 | 0.249872 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078143 | TGCCTGCCACCTGCT[C/T]GCCCCCACAGCAGTG | 221178 |
rs9511036 | snp | C/G | 0.178144 | 0.239451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081530 | AAAAAAAAAGCTGGC[C/G]CAGTGTGATGACTCA | 221178 |
rs9511037 | snp | C/G | 0.43598 | 0.167067 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083537 | TGTGGAGTTGAAGGT[C/G]GTTGGAGGTTTGTTG | 221178 |
rs9511038 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084451 | TGCGAGGTACACAGG[A/G]CACTTTTTGCACCCT | 221178 |
rs9511041 | snp | C/T | 0.363359 | 0.222822 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089808 | ATGTGTTTCTTGTGG[C/T]TCTCGAGATTGGAAG | 221178 |
rs9511042 | snp | C/T | 0.427575 | 0.175975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091143 | agaccttcagtactc[C/T]agcacacagttcaca | 221178 |
rs9511044 | snp | A/G | 0.342358 | 0.232314 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092735 | ATTTGGCAGCTTGCT[A/G]TTTCTACATGTTTTA | 221178 |
rs9511045 | snp | A/G | 0.346147 | 0.230772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092798 | AGCAGTCATATTTGG[A/G]CATCTGTATGTGGAG | 221178 |
rs9511049 | snp | C/T | 0.495368 | 0.0478996 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100536 | TCCTTCATCTTGTAG[C/T]GATGGAATGTTCTGA | 221178 |
rs9511050 | snp | C/T | 0.337386 | 0.23423 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102463 | ggttttttcatttgc[C/T]tcacagaatttcttt | 221178 |
rs9511051 | snp | C/T | 0.383053 | 0.211653 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102635 | gcccaccactaagcc[C/T]ggctatttttgtatt | 221178 |
rs9511052 | snp | G/T | 0.383246 | 0.211531 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102678 | ggggtttcaccacgt[G/T]ggccaggctggtctc | 221178 |
rs9511053 | snp | A/G | 0.383053 | 0.211653 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102754 | actgggattacaggc[A/G]tgagccaccacgccc | 221178 |
rs9511054 | snp | A/C | 0.38286 | 0.211774 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102798 | aaattttttaagttc[A/C]acataattccattag | 221178 |
rs9511055 | snp | A/C | 0.434831 | 0.168337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102804 | tttaagttccacata[A/C]ttccattagtttatt | 221178 |
rs9511056 | snp | C/G | 0.382473 | 0.212016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102839 | cttttgttgccgatg[C/G]ttttggtgttatacc | 221178 |
rs9511057 | snp | G/T | 0.392696 | 0.205275 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104593 | CTTTTCATTTACTCC[G/T]TCACTCATAGTGACA | 221178 |
rs9511062 | snp | A/T | 0.416708 | 0.186302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108973 | TTTATTTTATTTTTT[A/T]AAATTATACTTTAAG | 221178 |
rs9511063 | snp | A/T | 0.38286 | 0.211774 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115419 | TGCCTGAGCTCTGCC[A/T]CCTGTCAGATCATCA | 221178 |
rs9511067 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24123548 | TGGTTCTGTAAGAAT[C/G]TGGTAACAAAATCCT | 221178 |
rs9511068 | snp | A/G | 0.3512 | 0.228601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127324 | TGACCTTTAGTCAAG[A/G]GACAAAGCCATCCCA | 221178 |
rs9511069 | snp | A/C | 0.359787 | 0.224604 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128110 | AGCCTCTGACATATC[A/C]ACTGTAAATCCTGGA | 221178 |
rs9511070 | snp | C/T | 0.359787 | 0.224604 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128546 | GCCTCAGGTAGCTTT[C/T]TGAGAATAGCCTGTC | 221178 |
rs9511071 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128599 | CTCCACAGCCACGCC[A/G]GGCCCCAGAAATCTG | 221178 |
rs9511072 | snp | A/C | 0.371785 | 0.218331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129330 | GACTTTCATCCTTCA[A/C]TTCCCATGCTCAATT | 221178 |
rs9511075 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135426 | TTTAGGTCCAGGTGC[A/G]GTGGCTCACGCCTGT | 221178 |
rs9511076 | snp | A/G | 0.49706 | 0.0382258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135480 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 221178 |
rs9511077 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135570 | GGGCATGGTGGCAGG[C/T]GCCTGTAGTCCCAGC | 221178 |
rs9511081 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137700 | GGGGGCGGAGGTTGC[A/G]GTGAGCCAAGATCAT | 221178 |
rs9511082 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139955 | cacctgtagtcccag[C/T]tactcgggaggctga | 221178 |
rs9511083 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139967 | cagctactcgggagg[C/T]tgaggcaggagaatg | 221178 |
rs9511085 | snp | A/C | 0.375 | 0.216506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142790 | GGCATTTGGTAGGTC[A/C]CTCAAAAAGCTTAGG | 221178 |
rs9511086 | snp | A/G | 0.386884 | 0.209196 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143306 | TGGGAGGGAACCTAC[A/G]TTGCCCCTTCCCCCT | 221178 |
rs9511087 | snp | A/G | 0.47852 | 0.101384 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144278 | CCTCGTGTACGTCAC[A/G]AACATCACACCAAAG | 221178 |
rs9511088 | snp | C/T | 0.45762 | 0.139261 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145257 | ACAGCCACAAAATAC[C/T]AAGTAGACAGAGGCA | 221178 |
rs9511089 | snp | A/G | 0.454423 | 0.143914 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150577 | taaggaattgcacac[A/G]aatttgagggctggc | 221178 |
rs9511090 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155727 | caattttaagtgtgc[A/C]attcagtacattaag | 221178 |
rs9511091 | snp | C/T | 0.444533 | 0.157025 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156534 | TTCCCAGCACCCCAA[C/T]AGCCAAATAGATACT | 221178 |
rs9511092 | snp | C/T | 0.461592 | 0.133149 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157408 | ggttcacgccattct[C/T]ctgccttagcctccg | 221178 |
rs9511093 | snp | C/T | 0.461923 | 0.132621 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157415 | gccattcttctgcct[C/T]agcctccggagtagc | 221178 |
rs9511096 | snp | C/G | 0.241053 | 0.24984 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163370 | TTTTGCCACTACACT[C/G]CAGCCTGGGTGACAG | 221178 |
rs9511097 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163812 | CTATAGCTTGGTAGG[C/T]TGACCTCTCTGTTTG | 221178 |
rs9511098 | snp | G/T | 0.490943 | 0.0666801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164079 | GGAATGAACACCAAA[G/T]GTACATGGTTTTCTT | 221178 |
rs9511100 | snp | A/G | 0.176219 | 0.238865 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166542 | ACTATAGCCCCAAGC[A/G]CATCAGTCATGACTG | 221178 |
rs9511101 | snp | A/G | 0.261608 | 0.24973 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166980 | GTTCCCATCTCTCAG[A/G]GTTTCAAAACCTTTG | 221178 |
rs9511106 | snp | C/G | 0.0798192 | 0.183927 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173954 | ttttgatcaggtttt[C/G]gtaccagggaaatat | 221178 |
rs9511108 | snp | A/G | 0.359998 | 0.2245 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175505 | CCCAGCTTGATCTCA[A/G]AATCAGAGTCCAGAC | 221178 |
rs9511109 | snp | A/G | 0.372592 | 0.217879 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175544 | TTGCCAGTTAGGGCT[A/G]GAAGAAAGGGATGTG | 221178 |
rs9511110 | snp | A/G | 0.362104 | 0.223456 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176121 | GTGTGATTGTTACAA[A/G]GGTAGAGTCCAAGTG | 221178 |
rs9511111 | snp | A/T | 0.386694 | 0.20932 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177866 | ggatttcaacatatg[A/T]atttttttttaattg | 221178 |
rs9511112 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178962 | ccccagccctagaca[A/G]ccactcatctatagt | 221178 |
rs9511115 | snp | C/T | 0.451732 | 0.147663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187550 | gagcaagtctattgg[C/T]gccattcattgttac | 221178 |
rs9511116 | snp | C/G | 0.452719 | 0.146304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187760 | ttgtatatgttttga[C/G]tgcttcactgctggc | 221178 |
rs9511117 | snp | A/C | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187906 | gagtcgcccatctct[A/C]ttttaaatccaaagc | 221178 |
rs9511118 | snp | A/G | 0.454061 | 0.144427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188531 | tttaattctgtgaag[A/G]ctgagagaggtgaag | 221178 |
rs9511122 | snp | G/T | 0.221439 | 0.248363 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190898 | ctatcaaacagtatc[G/T]catcctgtagagaaa | 221178 |
rs9511123 | snp | A/T | 0.243061 | 0.249904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191277 | catcttgcccagcCA[A/T]attttaaaattaatg | 221178 |
rs9511124 | snp | C/G | 0.45235 | 0.146814 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192886 | ACTTCCAGAGCCCAG[C/G]AGGTGGTCCTGGGAG | 221178 |
rs9511125 | snp | A/C | 0.45235 | 0.146814 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192963 | CTGTTCTCAAAACAC[A/C]AAGCACTGTAACCGG | 221178 |
rs9511126 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193035 | GTCAAGGTGTGTGGG[C/T]TGAGAGCCCTGGGGG | 221178 |
rs9511127 | snp | A/G | 0.450357 | 0.149522 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193773 | GGTTAGTGTGGAAAC[A/G]TAGCTATTCCTCAGT | 221178 |
rs9511128 | snp | A/G | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194067 | ATCCATGGTTCAGTA[A/G]CCGAGTCTGTGGTGG | 221178 |
rs9511129 | snp | A/G | 0.453939 | 0.144598 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194179 | CTAGGCAAGACTGCA[A/G]TGGTACAGGCAGTGG | 221178 |
rs9511130 | snp | G/T | 0.454061 | 0.144427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194257 | AATGTGCAGCTAAAA[G/T]CGTCCTGAATGTTGT | 221178 |
rs9511131 | snp | A/C | 0.454423 | 0.143914 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194442 | ACTGGAAATGTTGAG[A/C]ATCACTGACAGAGCG | 221178 |
rs9511132 | snp | A/G | 0.455144 | 0.142885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194446 | GAAATGTTGAGAATC[A/G]CTGACAGAGCGAACC | 221178 |
rs9511133 | snp | C/T | 0.455144 | 0.142885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194464 | GACAGAGCGAACCAT[C/T]CAGCTCTGTGAAATA | 221178 |
rs9511134 | snp | C/G | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194491 | AATAGGAGAAACCAA[C/G]TAGCTGGAGAGGTAG | 221178 |
rs9511135 | snp | C/T | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195090 | AAGAAACCCCAATTC[C/T]TGTTAGCAGTCATTC | 221178 |
rs9511137 | snp | A/G | 0.482309 | 0.0923707 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197086 | GAGGGCACCTGAGAT[A/G]GGTATGATCTTACTG | 221178 |
rs9511138 | snp | A/G | 0.466927 | 0.124269 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197137 | CAGTCTTGAGAAAAG[A/G]CCCATCTTTAGAGGA | 221178 |
rs9511140 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198989 | ggtcttactctgtca[C/G]ccagtctggagtgca | 221178 |
rs9511141 | snp | C/T | 0.309648 | 0.24278 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199665 | gatgggaaaaacttg[C/T]gtcttgtgatctaag | 221178 |
rs9511143 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200509 | ACCTCGTTCTCAGCC[C/T]CAAGTCTCCCACCCA | 221178 |
rs9511144 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202301 | TTGATCTTCCTGCCT[C/T]TGAGCCCCAGAACCC | 221178 |
rs9511145 | snp | C/T | 0.190833 | 0.242898 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207014 | gaaaagtggtatgta[C/T]acaccatggaatact | 221178 |
rs9511147 | snp | C/G | 0.289424 | 0.246872 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208858 | AAGTCAAGTGAGAGT[C/G]TCAAGAGGTGAATAC | 221178 |
rs9511151 | snp | A/G | 0.291235 | 0.246576 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212438 | TCCTTGCTTCATGTG[A/G]TCCTGAAGTGCTTAT | 221178 |
rs9511154 | snp | A/G | 0.277067 | 0.24853 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214059 | ACCTTCTCCAGATCC[A/G]CATTCAGGTGATCTT | 221178 |
rs9511156 | snp | A/G | 0.0948699 | 0.196048 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223648 | GTGAGATTCTCGTGA[A/G]GGACCCTGAAAACAA | 221178 |
rs9511157 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225874 | GCCATCCGGGAAAgt[A/G]ttacagctcctttcg | 221178 |
rs9511160 | snp | A/G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233977 | ATAAAATTATCGTAT[A/G/T]CCTGTAGTTTTGAAC | 221178 |
rs9511163 | snp | A/G | 0.135825 | 0.222405 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237124 | gcactttctgaggcc[A/G]aggtgggtgaatcat | 221178 |
rs9511165 | snp | A/G | 0.474634 | 0.109726 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247608 | CCGCCTCAGCCCCCC[A/G]AGTAGCTGGGATTAC | 221178 |
rs9511169 | snp | C/T | 0.155325 | 0.23138 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260793 | GGAAATCATAGCGGA[C/T]GCATATGGGTGTGGA | 221178 |
rs9511172 | snp | A/C | 0.499234 | 0.0195537 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264841 | AGCTGGCACCTTTTA[A/C]AGGACAATTTTATAT | 221178 |
rs9511173 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273221 | GAGACGGGACAGAGG[C/T]TGAGTTTTGAGAGCA | 221178 |
rs9511175 | snp | C/T | 0.301932 | 0.244547 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279329 | GAGAGGGGTGGGAGG[C/T]ACAGTGTATCTGGGG | 221178 |
rs9511176 | snp | G/T | 0.214843 | 0.247516 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279810 | ATTTTCACTCCAGGC[G/T]CCATGACTTTCCCTC | 221178 |
rs9511178 | snp | G/T | 0.279991 | 0.248195 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282711 | AGCCCAGCCCTCATC[G/T]TGCGGGACACCATCA | 221178 |
rs9511179 | snp | C/T | 0.302435 | 0.244439 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283031 | CCTTCTGTGTGCCCC[C/T]GATCTTTGCAGTCTT | 221178 |
rs9511180 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287402 | TCATGGACTGAAGCA[A/C]TTTTCCTGCCTTGAT | 221178 |
rs9511181 | snp | C/T | 0.438946 | 0.163706 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293433 | CAGCTTAGTACATTC[C/T]GAGATGGGAAAGCTG | 221178 |
rs9511182 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299513 | TGGAGGCAGGGACAG[C/T]CCGGTGGCCAGCGTA | 221178 |
rs9511184 | snp | C/T | 0.337386 | 0.23423 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306154 | CTTATTCAGAAAATC[C/T]CCCCATCCTACATGA | 221178 |
rs9551033 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999364 | acagatcctcatttt[C/T]taccaaaaaaaaaaa | 221178 |
rs9551034 | snp | A/G | 0.391583 | 0.206044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003218 | GTACCTATAGATAGA[A/G]AGGGGAGTGCCTAGG | 221178 |
rs9551035 | snp | A/T | 0.391583 | 0.206044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003365 | TAACAGCAGGTTTAC[A/T]AGAGAAGGTGGTAAA | 221178 |
rs9551036 | snp | C/T | 0.391397 | 0.206172 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003374 | GTTTACAAGAGAAGG[C/T]GGTAAAAAGATTGAG | 221178 |
rs9551037 | snp | A/G | 0.391583 | 0.206044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003455 | TCATGAGGAACCTGA[A/G]TTAAGGCTGCTGTGC | 221178 |
rs9551038 | snp | A/G | 0.391583 | 0.206044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003513 | CTTTGGAAGCATGTA[A/G]AGGCTTTAAGATAAC | 221178 |
rs9551039 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24014676 | TTCTCCTAAAATTTA[C/G]TATTGTTATTTAACA | 221178 |
rs9551040 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019160 | GTGGCGGGATCTCGG[C/T]TCACTGTAAGCTCCG | 221178 |
rs9551041 | snp | A/G | 0.412917 | 0.189626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027671 | TTCTAGTATAAGCAA[A/G]TAAGCCTCTTTTCTG | 221178 |
rs9551042 | snp | A/G | 0.141596 | 0.225274 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041850 | GAGCAAAGGGCAGAG[A/G]AGACTTGGCCACCAA | 221178 |
rs9551043 | snp | C/T | 0.137527 | 0.223271 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042150 | GTGTCACGGGAGCGT[C/T]GGCTATGACCACCTA | 221178 |
rs9551044 | snp | G/T | 0.137187 | 0.223099 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042167 | GCTATGACCACCTAG[G/T]GTGGGTTGTGAGAGA | 221178 |
rs9551045 | snp | C/T | 0.274929 | 0.248754 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057059 | CGTCTGGCTCTTTCT[C/T]TTTTTTTTTTCTTTT | 221178 |
rs9551046 | snp | A/G | 0.346147 | 0.230772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057314 | TTCTCGGCCTGTGGC[A/G]CTTTGCACTCCCACT | 221178 |
rs9551047 | snp | C/G | 0.328382 | 0.237395 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057356 | TCCTCTTGACAAAGT[C/G]CTGAATTTTCCCCCT | 221178 |
rs9551048 | snp | A/G | 0.383439 | 0.21141 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062617 | TTCCGTTTTCTTATA[A/G]AAGTCGGGCTTCGGT | 221178 |
rs9551049 | snp | A/T | 0.330714 | 0.236612 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068790 | gagctctttttcata[A/T]gtttgttggccgcat | 221178 |
rs9551050 | snp | A/T | 0.330016 | 0.236849 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069112 | ctgtttgggctcttt[A/T]ttgatttcatatgaa | 221178 |
rs9551051 | snp | A/G | 0.332337 | 0.236052 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071671 | CCTGCATTGAATCAC[A/G]TCAGATTTAATGTTC | 221178 |
rs9551052 | snp | A/G | 0.330714 | 0.236612 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074125 | acatccaatcttcag[A/G]acatcttgaagatct | 221178 |
rs9551053 | snp | A/G | 0.458775 | 0.137524 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076920 | CAGTCATTGCAGCAG[A/G]TCGGCTCTTCAACCT | 221178 |
rs9551054 | snp | A/T | 0.429698 | 0.173807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077626 | ATCTAAAATAAAATT[A/T]AAAAAAAAAAGACAA | 221178 |
rs9551055 | snp | G/T | 0.400682 | 0.199487 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078782 | GCTGTTATCCCAGTT[G/T]TGTGATGGGGTTCAG | 221178 |
rs9551056 | snp | A/G | 0.41141 | 0.19091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079048 | TTTGGCCTAACCAGA[A/G]AATTGGAGAGGGCTT | 221178 |
rs9551057 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092591 | AAAGGCAATCAGAAA[A/G]CCCATTTTAGGGTCT | 221178 |
rs9551059 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099619 | GGCCCACAGCCCCCC[A/G]GGTGGTGTTTCCAGA | 221178 |
rs9551060 | snp | A/G | 0.493613 | 0.0561475 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106135 | AGCTCCTGGACTCTT[A/G]CAACCCTCCTGCCCC | 221178 |
rs9551062 | snp | A/G | 0.29278 | 0.246313 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116586 | tgtatctaggagttc[A/G]ttttaccctcatttt | 221178 |
rs9551063 | snp | C/T | 0.24019 | 0.249807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116723 | GGTTCACCATtgcca[C/T]agacttaactgtgtc | 221178 |
rs9551064 | snp | C/T | 0.29046 | 0.246704 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122369 | CATCAACAGGGTTAT[C/T]TTCATCATCAATGAT | 221178 |
rs9551065 | snp | A/G | 0.314301 | 0.241589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130689 | TGCTGACGGTTTAAC[A/G]GTGGTTTAGAAAGAG | 221178 |
rs9551066 | snp | C/G | 0.33533 | 0.234987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130693 | GACGGTTTAACGGTG[C/G]TTTAGAAAGAGCACA | 221178 |
rs9551067 | snp | A/G | 0.493925 | 0.054776 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130782 | ACCTGCAAACACGCT[A/G]TTTTCCTGGACCTAA | 221178 |
rs9551068 | snp | A/G | 0.493925 | 0.054776 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130792 | ACGCTATTTTCCTGG[A/G]CCTAAATAAGTGCCC | 221178 |
rs9551070 | snp | C/T | 0.3746 | 0.216737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142506 | CTGTTAGATTGAGGT[C/T]ATGCATTTGGGGGCA | 221178 |
rs9551072 | snp | G/T | 0.34437 | 0.231505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156714 | GAGCATTTGACCACG[G/T]GCCAGGCAGTGAGCT | 221178 |
rs9551073 | snp | C/T | 0.405255 | 0.195948 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181808 | aaagcatacacttta[C/T]atgaactataaaaag | 221178 |
rs9551076 | snp | C/T | 0.151668 | 0.229849 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190574 | tgactttgaggggtt[C/T]gagacttcagtggag | 221178 |
rs9551077 | snp | A/G | 0.187685 | 0.242109 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197381 | TGTTAAAACGTAACT[A/G]TCTCTTAAATGTATC | 221178 |
rs9551078 | snp | G/T | 0.493748 | 0.0555599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203330 | GGTAATTTAGGGGAA[G/T]GGGAAGAAGGGGAAG | 221178 |
rs9551079 | snp | A/G | 0.493748 | 0.0555599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203378 | CACTCAACTTTTTAA[A/G]TAGCTTTTTCCTAAA | 221178 |
rs9551080 | snp | C/T | 0.495016 | 0.0496707 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203635 | AGGCAAGAATCAGGA[C/T]AGGGTAATTTCTGGG | 221178 |
rs9551081 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239383 | GCCAGGGACAGGAGA[G/T]TATGAAAATGTAAAG | 221178 |
rs9551082 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239515 | gcttgggcaacatgg[C/G]gaaactctgtctctg | 221178 |
rs9551083 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239526 | atggcgaaactctgt[C/T]tctgctaaaactaga | 221178 |
rs9551084 | snp | A/G | 0.46137 | 0.133501 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239969 | TTTCATAATATGATG[A/G]CTTTAAACTGTCTCT | 221178 |
rs9551086 | snp | C/T | 0.483199 | 0.0901004 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256192 | AGTATATTTCTCCTC[C/T]CTGGTCAAGTATTCT | 221178 |
rs9551087 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273195 | GCCAACGACGCCCCA[G/T]CTCTGAACTGGAGAC | 221178 |
rs9551089 | snp | A/G | 0.440884 | 0.161442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281545 | ATGGGCCATGCCTCA[A/G]TGTGGCGTGTGCTGT | 221178 |
rs9551090 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292993 | agagtgagactttgt[C/T]tcaaaaaaaaaaaaa | 221178 |
rs9553129 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982270 | CCTGGCTGGTCCTGC[A/G]TGAAGACTTTGCTAT | 221178 |
rs9553131 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992761 | CCTGGCAAACTCACA[C/T]CCATAGTTGGATGGA | 221178 |
rs9553133 | snp | C/T | 0.391769 | 0.205917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001613 | CTTCCCAGGAGACCC[C/T]AGCAGAGACCCACCA | 221178 |
rs9553134 | snp | A/G | 0.38821 | 0.208322 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001821 | AGGGGTGAGGACTGA[A/G]CAGGTGATCTGTGGG | 221178 |
rs9553135 | snp | C/T | 0.396727 | 0.202413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001833 | TGAGCAGGTGATCTG[C/T]GGGGAGAGGCTCCGG | 221178 |
rs9553136 | snp | C/T | 0.336702 | 0.234484 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002416 | GGGAAATGTCACAGT[C/T]GCTCTGCATTCCATA | 221178 |
rs9553137 | snp | A/G | 0.391397 | 0.206172 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002554 | CTGAGGCCTGGTCAG[A/G]GGGGTGAGTGTGTTG | 221178 |
rs9553138 | snp | A/G | 0.390277 | 0.206936 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002725 | CACCTGTGACCCCCC[A/G]AGCACAAGCACTGGC | 221178 |
rs9553139 | snp | C/T | 0.391024 | 0.206427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002866 | GTAAAATCAAACTCA[C/T]TGGTCATCCCTGGGT | 221178 |
rs9553140 | snp | C/T | 0.391769 | 0.205917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003876 | CACAATATACATCAG[C/T]AAATACAGAACCCAT | 221178 |
rs9553141 | snp | A/G | 0.143284 | 0.226079 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010112 | ctcgaagtggggagg[A/G]ggcttccaggtcata | 221178 |
rs9553142 | snp | C/T | 0.367091 | 0.220884 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010496 | tgtagctacgttatt[C/T]agttggatctggaat | 221178 |
rs9553143 | snp | C/G | 0.443866 | 0.157848 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017415 | CAGTGTGATCTAAAT[C/G]TAAATCTCTTGGGCA | 221178 |
rs9553144 | snp | C/G | 0.412917 | 0.189626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027804 | AAATTAGTATATGCA[C/G]GGATCTTAGAAGAAC | 221178 |
rs9553145 | snp | C/G | 0.412917 | 0.189626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027922 | TCTGCTCCAGCATCT[C/G]CCATGTAACACCAGA | 221178 |
rs9553146 | snp | A/G | 0.135825 | 0.222405 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029313 | gcttttaccagatgc[A/G]tcaggacagtacaaa | 221178 |
rs9553147 | snp | C/G | 0.150333 | 0.229274 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034662 | CACAGTCATTGGGAG[C/G]TTCACCAGGTGGAAG | 221178 |
rs9553148 | snp | C/T | 0.326976 | 0.237854 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037510 | TCTTCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 221178 |
rs9553149 | snp | G/T | 0.498158 | 0.0302955 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042125 | TTGCTGAGAAAGCGC[G/T]GTGTCCTCTGTGTCA | 221178 |
rs9553150 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043472 | GGTTCTGGACCTTGA[C/T]TGATATTACACACAC | 221178 |
rs9553151 | snp | C/G/T | 0.274393 | 0.248807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056974 | TTTCTGGGAAAAACT[C/G/T]GAGCCACAGACACAT | 221178 |
rs9553152 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057029 | TCTCTCTCTCTCTCT[C/T]TCTTTCTTTCATAGC | 221178 |
rs9553153 | snp | C/G | 0.328382 | 0.237395 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057231 | AGCTATCCCTCCCCC[C/G]TCCCCCCAACCCCAC | 221178 |
rs9553154 | snp | A/G | 0.308414 | 0.24308 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060971 | ttgaaccttggaggc[A/G]gaggttgcagtgagc | 221178 |
rs9553155 | snp | C/G | 0.491316 | 0.0653198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066923 | GCAAACCAAACCAAG[C/G]AGAGGCCTGGGGTTG | 221178 |
rs9553156 | snp | A/T | 0.491368 | 0.0651254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067727 | gttttgtttttgaga[A/T]ggagtctcactctgt | 221178 |
rs9553158 | snp | A/T | 0.330249 | 0.23677 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070541 | GCCTTACTTTGGGAC[A/T]ATGTGTTTATTGTGA | 221178 |
rs9553159 | snp | C/T | 0.332106 | 0.236133 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075850 | AAGCATTTGCCGCCA[C/T]GCTGTCTCCCTTTAT | 221178 |
rs9553160 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076622 | CTCTGGTGACCCGGG[A/G]TCTGGGGTGGTGCTG | 221178 |
rs9553161 | snp | A/G | 0.389903 | 0.207189 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078032 | CTAACTTTGCAAACC[A/G]GTCCCAGCGTCCATG | 221178 |
rs9553162 | snp | A/G | 0.332568 | 0.235971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079082 | GGAGGAGGTGGTACT[A/G]ATCTGATAACGGAGG | 221178 |
rs9553163 | snp | A/G | 0.381503 | 0.21262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082405 | GTCTGTGGCGGGGAG[A/G]GTAACACTGATGGAG | 221178 |
rs9553164 | snp | G/T | 0.498754 | 0.0249289 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087694 | TCTCTACACACACGC[G/T]TCTCTAGGTCACAGA | 221178 |
rs9553165 | snp | A/G | 0.106987 | 0.205054 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088512 | CACCATGTGTTGATC[A/G]TTGGGTCCACAGCCC | 221178 |
rs9553166 | snp | A/G | 0.190833 | 0.242898 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093562 | AAAGATCAGGCCCAA[A/G]ATGCTCCATTGAAAT | 221178 |
rs9553167 | snp | A/T | 0.110519 | 0.207473 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093915 | TGCAGCCTCAACTGT[A/T]ATCAGACTATATACC | 221178 |
rs9553169 | snp | A/C | 0.111224 | 0.207945 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095149 | gccaagaggcggaaa[A/C]aacccaagtgtccat | 221178 |
rs9553170 | snp | A/G | 0.267908 | 0.249358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096227 | ggagcttatagtctc[A/G]ggaggatatcaacat | 221178 |
rs9553171 | snp | A/T | 0.482979 | 0.0906686 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097239 | ctatatgccaggctt[A/T]gtgctaaacatgttg | 221178 |
rs9553172 | snp | A/T | 0.472989 | 0.113031 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098383 | ggcaagaccccttct[A/T]ttaaaaaaataatta | 221178 |
rs9553173 | snp | C/T | 0.469148 | 0.120308 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098578 | gtcctgcctaggaga[C/T]agagtgagactgtct | 221178 |
rs9553174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100761 | TTGCTCTTACCTGAG[C/T]TCCTCACTCCCGTGC | 221178 |
rs9553175 | snp | C/T | 0.380138 | 0.213458 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102980 | atcaggactcaactt[C/T]aAGTTAAACAATTTT | 221178 |
rs9553176 | snp | C/T | 0.380333 | 0.213338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102986 | actcaactttattcc[C/T]ttgcatgtggctatc | 221178 |
rs9553177 | snp | C/G | 0.335559 | 0.234904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103833 | CAGAGAATTTTCATC[C/G]CTTTCAGAGTTACAG | 221178 |
rs9553179 | snp | A/G | 0.420733 | 0.18262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109731 | CTTTTTTGCCCCCCA[A/G]ATTACATGGATAGAC | 221178 |
rs9553180 | snp | A/G | 0.420574 | 0.182769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109798 | TGTACATTTTACTCT[A/G]GTAAATACATCTGCA | 221178 |
rs9553181 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111938 | GGTTATACTGCCTCT[A/G]TCCAATCAGCGGAAG | 221178 |
rs9553182 | snp | C/T | 0.477175 | 0.104362 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112341 | TGCTCTTGTTGCCCC[C/T]ACAGCACCTTCTGTG | 221178 |
rs9553183 | snp | C/T | 0.341235 | 0.232758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114929 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 221178 |
rs9553184 | snp | C/T | 0.240478 | 0.249819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115230 | GGTCTTCCAGGTGCC[C/T]CTCACAGCAGCAGTC | 221178 |
rs9553185 | snp | A/G | 0.231189 | 0.249291 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115379 | TAGGAACCTGACTGC[A/G]CAGCAGAAGGTGAGT | 221178 |
rs9553186 | snp | C/G | 0.400147 | 0.19989 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120562 | AGCTGCCTGGCCTTG[C/G]GTGAGCCACTATACC | 221178 |
rs9553187 | snp | A/G | 0.399968 | 0.200024 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120573 | CTTGGGTGAGCCACT[A/G]TACCACCCTCTGCCT | 221178 |
rs9553188 | snp | G/T | 0.40086 | 0.199352 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120963 | TCTAGGTCTGAGGAA[G/T]AAAACTGCAAGATAA | 221178 |
rs9553189 | snp | C/T | 0.395453 | 0.203331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124667 | TTTCCAAGTTTGGTT[C/T]AGCAATTCTATATTG | 221178 |
rs9553190 | snp | A/T | 0.361474 | 0.223771 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126548 | ATTTGTGTGTGTGTG[A/T]GAGAGAGAGACAGAC | 221178 |
rs9553191 | snp | A/G | 0.286564 | 0.247312 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127179 | ATAAGGGAGTTATTT[A/G]CAAAGGTGTGGCCAG | 221178 |
rs9553192 | snp | G/T | 0.030278 | 0.119257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128486 | TAATTAAATGGTGGG[G/T]CAGAGCCATTAGGAA | 221178 |
rs9553193 | snp | A/G | 0.358303 | 0.225323 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128659 | GGCCTTGTTGTGGAA[A/G]CAGGACTCCCGGGAG | 221178 |
rs9553194 | snp | A/T | 0.429837 | 0.173662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129513 | TTTGCAGACCGGAGG[A/T]TTGCTGGAGGCCTAA | 221178 |
rs9553195 | snp | A/G | 0.314301 | 0.241589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130173 | GGTGCTCAGCACTTC[A/G]TGTGAAGGGAATCAT | 221178 |
rs9553196 | snp | C/T | 0.493925 | 0.054776 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130772 | AATCAACAGAACCTG[C/T]AAACACGCTATTTTC | 221178 |
rs9553197 | snp | C/T | 0.494013 | 0.0543839 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132025 | TCAGCCAATGAGATG[C/T]GCTTGAGTGACAGAC | 221178 |
rs9553199 | snp | A/G | 0.251859 | 0.249993 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136694 | CCTATTGGGCTCTGA[A/G]AGATAGGCcccagca | 221178 |
rs9553200 | snp | A/G | 0.367503 | 0.220665 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140233 | AGCCTAGTCGTTTAG[A/G]TTAAAGTTCATTTAT | 221178 |
rs9553201 | snp | C/T | 0.381113 | 0.21286 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143006 | GGGTTCACACAGAAG[C/T]TGACCCTGAGACAAT | 221178 |
rs9553203 | snp | A/C | 0.339882 | 0.233284 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155510 | CTCGGTGCCTAGATT[A/C]ATTATTTAAAGTGGG | 221178 |
rs9553204 | snp | C/T | 0.266 | 0.249487 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164607 | AACTGAGGAGCAAGT[C/T]AAGTTTCATTGCTCC | 221178 |
rs9553205 | snp | A/G | 0.306679 | 0.24349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169903 | GAGCACTTCTGTGCC[A/G]TGAACACCTGCCTTC | 221178 |
rs9553206 | snp | C/T | 0.298398 | 0.245271 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174391 | gcttagtttgctttt[C/T]ttttctagatttttg | 221178 |
rs9553207 | snp | A/G | 0.448066 | 0.152544 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175088 | ttggtccatcttgat[A/G]TGCATTAATCCTGCA | 221178 |
rs9553208 | snp | C/T | 0.355096 | 0.226837 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176587 | AGGACAGATTAAGCA[C/T]GCTGGGTCCTGGCAG | 221178 |
rs9553209 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186645 | TCAGAGTTTCTTAAC[C/T]TTCAGTGTCAGGAGG | 221178 |
rs9553210 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188620 | taacataagtgcagg[A/G]tgaagcagcaagtgc | 221178 |
rs9553211 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190311 | tatattattatatat[A/C/T]atatataatattata | 221178 |
rs9553212 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190323 | tataatatataatat[A/T]atatattattatata | 221178 |
rs9553213 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190358 | atataatattatata[A/T]tattatatataatat | 221178 |
rs9553214 | snp | G/T | 0.305685 | 0.24372 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190617 | gatgtggtggaaaca[G/T]caagagaactggaat | 221178 |
rs9553215 | snp | C/G | 0.211516 | 0.24702 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197071 | GCCAAATAACAACCA[C/G]AGGGCACCTGAGATG | 221178 |
rs9553216 | snp | A/C | 0.472522 | 0.113946 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200382 | CTTAGCTGTTTTATT[A/C]AATACTTAATTCATA | 221178 |
rs9553218 | snp | A/G | 0.404733 | 0.196361 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207103 | gccattatcctcagc[A/G]aactaaagcaggaat | 221178 |
rs9553219 | snp | A/T | 0.404733 | 0.196361 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207110 | tcctcagcaaactaa[A/T]gcaggaatagaaaac | 221178 |
rs9553220 | snp | C/T | 0.404733 | 0.196361 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207118 | aaactaaagcaggaa[C/T]agaaaaccaaataca | 221178 |
rs9553221 | snp | C/G | 0.291493 | 0.246533 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215283 | AAACAATATGCAAAT[C/G]TCAGTTCAATTAGAA | 221178 |
rs9553222 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24236232 | TAGAATTAAATGCAT[C/T]TACTTCAGAGAGTTT | 221178 |
rs9553223 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237944 | acatgtttaaatatg[C/T]aAAGTGATGTGCTGT | 221178 |
rs9553224 | snp | G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241167 | CTAGTAAAAAATGCA[G/T]CACATTTGTAAGAGT | 221178 |
rs9553225 | snp | A/G | 0.392696 | 0.205275 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248868 | ATTTTACTAATTCAC[A/G]ATGGTGCTGATTTTC | 221178 |
rs9553226 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277438 | aacagagcaagactc[C/T]gtctcaaaaaaaaaa | 221178 |
rs9553227 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278934 | tccttccctctttcc[C/T]tccttccttccttcc | 221178 |
rs9553228 | snp | C/T | 0.49917 | 0.0203505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280766 | TTGGAGTCTAAAACA[C/T]ACTCATGCATGAAAA | 221178 |
rs9553233 | snp | C/T | 0.397119 | 0.202129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294910 | CCATGCCACTCGCCC[C/T]TCCCGCACCTTTGAT | 221178 |
rs9553234 | snp | A/G | 0.449473 | 0.150701 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294924 | CTTCCCGCACCTTTG[A/G]TCTGGTGCAGATGCA | 221178 |
rs9553235 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298403 | CACACCCAGTGTTAC[A/G]TTTGTACTTCTTTGG | 221178 |
rs9578663 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978871 | aactaattaaaaaaa[A/T]ttttttttttggtag | 221178 |
rs9578667 | snp | C/T | 0.184838 | 0.241358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012788 | GTTGCCACAGCAATG[C/T]CCAGAACACCACCCT | 221178 |
rs9578668 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015322 | ACATGACATTATTTA[A/T]TTTTTTTCCCAAATA | 221178 |
rs9578669 | snp | C/T | 0.190519 | 0.242821 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025848 | ggagtctcactctat[C/T]gcctgggctggagtg | 221178 |
rs9578670 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037401 | AGGTTCTCGACTAAT[A/T]Ctttatttatttatt | 221178 |
rs9578671 | snp | A/G | 0.496314 | 0.0427728 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044142 | GCCTGAGCCTGGCCC[A/G]GGGCTGCTGTGCTGC | 221178 |
rs9578672 | snp | A/C | 0.342806 | 0.232136 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044352 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 221178 |
rs9578673 | snp | A/T | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047117 | actgagtccacctca[A/T]ggcggggtccacagg | 221178 |
rs9578674 | snp | C/T | 0.338523 | 0.233803 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052098 | ATCCTGTGCTGTGTC[C/T]AGGCTCCTCGGGTCT | 221178 |
rs9578675 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075894 | CTGGGAGAAGAGAGA[C/T]TTCTATAGAAGAAAT | 221178 |
rs9578676 | snp | A/G | 0.206336 | 0.246157 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077514 | GAAGAAAAATTTCCT[A/G]TCAGGTACAATCACC | 221178 |
rs9578677 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082674 | aaatacaaaaaatta[C/G]ccgggcgcggtggcg | 221178 |
rs9578678 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082855 | AAAAAAAAAAAAAAA[A/T]AAGATCTTTGCATTA | 221178 |
rs9578679 | snp | A/G | 0.129664 | 0.219133 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093945 | CTCAGGCCTCTCCCC[A/G]TCCCGGAGGTTAGAT | 221178 |
rs9578680 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102174 | ttgatcgtagccact[C/T]taacaggtgtgagtg | 221178 |
rs9578681 | snp | A/C | 0.153665 | 0.230694 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102888 | accaacatcgtggag[A/C]cttttccctatgttt | 221178 |
rs9578682 | snp | A/G | 0.157642 | 0.232314 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110568 | TAAGGCGGTGGAGAA[A/G]CAGGGTTTGTGGGTA | 221178 |
rs9578683 | snp | A/G | 0.41141 | 0.19091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113747 | TGGTGGTGCATGCCT[A/G]TAATCCCACCTACTC | 221178 |
rs9578684 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140305 | GGGAGGTCAAGAGCT[C/T]TGATGCATGCTGAGA | 221178 |
rs9578685 | snp | G/T | 0.468148 | 0.122112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172026 | aatggtggaactaag[G/T]atcttgacgtggata | 221178 |
rs9578687 | snp | C/T | 0.464523 | 0.128375 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185776 | CTCCAGAGAAAGAAC[C/T]AAAAGAATGTGTGTG | 221178 |
rs9578689 | snp | G/T | 0.078151 | 0.181571 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192880 | GGAGGCACTTCCAGA[G/T]CCCAGCAGGTGGTCC | 221178 |
rs9578691 | snp | A/C | 0.184521 | 0.241273 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198076 | tctctgcttactgca[A/C]cctccacctcccgga | 221178 |
rs9578692 | snp | C/T | 0.24019 | 0.249807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212114 | TAGGAAGTTCTTTCT[C/T]GTTCAGAGATGAAGG | 221178 |
rs9578694 | snp | A/T | 0.132066 | 0.220435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213810 | GAATCTTATAGGAAA[A/T]AATGTGTCTTCAAGT | 221178 |
rs9578695 | snp | C/T | 0.419936 | 0.183362 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227171 | TAAACACCCTACCTG[C/T]GCCACTCGTAGTTTG | 221178 |
rs9578696 | snp | A/G | 0.0422178 | 0.139109 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236494 | cagctactcggggag[A/G]ctgaggcaggagaat | 221178 |
rs9578697 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240433 | GGGGGAAAAACCTAT[C/T]AGCCTGGGAGTGTTG | 221178 |
rs9578698 | snp | A/G | 0.00506638 | 0.0500752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286752 | TCACCTGTCCCCTGT[A/G]TGTGGGTTGCAGTTG | 221178 |
rs9578699 | snp | A/G | 0.495407 | 0.0477027 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303041 | CCAGATGTGGGACCC[A/G]GTACCATGCTCTAAA | 221178 |
rs9578700 | snp | A/G | 0.49533 | 0.0480965 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303170 | GAGTGATGAGGTTAG[A/G]GGATCACTTCTGCAT | 221178 |
rs9578701 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304029 | GCACTCTCAAAGAGC[C/T]GCACTGCTCCTGACA | 221178 |
rs9580821 | snp | A/T | 0.308166 | 0.243139 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994366 | CTATTGTATAGAGGG[A/T]GGAATGAGACAATCT | 221178 |
rs9580822 | snp | A/G | 0.306431 | 0.243548 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994651 | TCTGTTCATCATTGA[A/G]TAATGAAGGTGAGAA | 221178 |
rs9580824 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000496 | AGGGCAGATAGAGCC[C/T]TTGCCATCCCCAAAC | 221178 |
rs9580825 | snp | A/G | 0.093777 | 0.195178 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011897 | GACCCAGAATGCTCA[A/G]CCTTCTTCTTTAAAC | 221178 |
rs9580826 | snp | A/G | 0.081446 | 0.184634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013574 | TTCCTGACCTTGTGA[A/G]TTCTTCCAAGATCTT | 221178 |
rs9580827 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014029 | AAAGGGGCTGTATAC[A/G]CTTGCTAGGGCTGCT | 221178 |
rs9580828 | snp | A/G | 0.104859 | 0.203554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014147 | CCTTTTGCAGGTGCC[A/G]GGGAAGGTCGGGGCC | 221178 |
rs9580829 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015749 | GGCAGGCCCCCCCCC[A/C]ATTCCTAGGTCCACC | 221178 |
rs9580830 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023670 | agagggaggctggac[A/G]ggaggccagagagat | 221178 |
rs9580831 | snp | C/T | 0.234982 | 0.249549 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030835 | AGCAGTGGAAAAGAC[C/T]TTTATGTAGGTAATC | 221178 |
rs9580832 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037402 | GGTTCTCGACTAATA[A/C]tttatttatttattt | 221178 |
rs9580833 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037640 | gtctcaatctcctga[C/G]ctcgtgatccacctg | 221178 |
rs9580834 | snp | A/G | 0.47023 | 0.118317 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041179 | ACCCACAGTAGCTCA[A/G]AACCACACTGGAAAA | 221178 |
rs9580835 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041898 | GCAGGTGGAATCAGA[A/G]TGAGGCGTAACGGTC | 221178 |
rs9580836 | snp | G/T | 0.495855 | 0.045338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041971 | GCTGTTCGAAAAATG[G/T]TGCCTAAAGCCTGTT | 221178 |
rs9580837 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042046 | CACAGAGGCAGCCAC[A/G]TGTGTCACATTTCAA | 221178 |
rs9580838 | snp | G/T | 0.496175 | 0.0435625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042099 | GCAGCGCAAGCTCCC[G/T]TCAGGCACATTTGCT | 221178 |
rs9580839 | snp | A/T | 0.496105 | 0.0439572 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042513 | GAGATCAGAGACACA[A/T]GTGCACGTCCACCAC | 221178 |
rs9580840 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042570 | ACAAGCGCACATCTA[C/T]GCCCGTGCGCGAACT | 221178 |
rs9580841 | snp | C/T | 0.492727 | 0.0598633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044136 | GTGGCTGCCTGAGCC[C/T]GGCCCGGGGCTGCTG | 221178 |
rs9580842 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044151 | TGGCCCGGGGCTGCT[C/G]TGCTGCAAGCCACAC | 221178 |
rs9580843 | snp | A/T | 0.34989 | 0.229177 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045872 | TCTCAGATGAACTGA[A/T]TCCATTCTGAGCCTC | 221178 |
rs9580844 | snp | A/T | 0.495927 | 0.0449436 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046041 | AATACAAAGCATTGC[A/T]TGTTCTGTTTCATAA | 221178 |
rs9580845 | snp | C/T | 0.495927 | 0.0449436 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046213 | aaacagcctcagaaa[C/T]cctcctcctgtcacc | 221178 |
rs9580846 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046347 | caccaggctggagtg[C/T]agtggtgtgattata | 221178 |
rs9580847 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046348 | accaggctggagtgc[A/G]gtggtgtgattatag | 221178 |
rs9580848 | snp | C/T | 0.350546 | 0.22889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047115 | gcactgagtccacct[C/T]aaggcggggtccaca | 221178 |
rs9580849 | snp | G/T | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047191 | tgccagaatgcagaa[G/T]tctgaaaaacatctc | 221178 |
rs9580851 | snp | C/T | 0.109108 | 0.206518 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054830 | AATGAATTCAGTCAC[C/T]TATGAAGTGTAACCT | 221178 |
rs9580852 | snp | C/T | 0.108755 | 0.206276 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058001 | GGAGATGTTCATGGC[C/T]AAATTCAAGCCTGGC | 221178 |
rs9580853 | snp | A/C | 0.117537 | 0.212022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061315 | agtaatgtagcaatt[A/C]ttcaaagagctaaaa | 221178 |
rs9580854 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066099 | AATTGATTATGAATT[A/G]TTAAAGGTACATACC | 221178 |
rs9580856 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083004 | GACTATAAATCTAAA[C/T]GTTTAATGGTTGGAA | 221178 |
rs9580858 | snp | A/T | 0.113334 | 0.209338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084771 | acatctgtaatccca[A/T]cactgtgagaagcca | 221178 |
rs9580859 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089078 | AATTGGCAGTTTTCA[C/T]AGATGAGGACACCAG | 221178 |
rs9580860 | snp | G/T | 0.0832709 | 0.186283 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090078 | gtttcaacacaagaa[G/T]tttgggaaagcttca | 221178 |
rs9580861 | snp | A/G | 0.104859 | 0.203554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090179 | TCAGATTTCCCCCCA[A/G]TTCTCTGCACTTGGA | 221178 |
rs9580862 | snp | A/T | 0.108048 | 0.20579 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090313 | CAGGGTTTGGTGTTA[A/T]TGGAGCTTCCCCTTT | 221178 |
rs9580863 | snp | C/T | 0.104504 | 0.2033 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090485 | CGTCCCCTCACCGAA[C/T]GGTGTCCTCACCTGA | 221178 |
rs9580864 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091630 | agtttggccaacatg[G/T]tgaaacctcgtttct | 221178 |
rs9580865 | snp | C/T | 0.108402 | 0.206034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093016 | TGATTAATCTTATTT[C/T]CCAGAGCATCCTGGT | 221178 |
rs9580866 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096459 | aaaaaaatagctggg[C/T]gtggtggcaggcacc | 221178 |
rs9580867 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098788 | aaaaattagctgggc[A/G]ttttggtgcgtgcat | 221178 |
rs9580868 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105711 | ccctaacattcatag[G/T]tcaaagccctaatcc | 221178 |
rs9580869 | snp | C/T | 0.326741 | 0.23793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107327 | AAAATGCTGTATGTA[C/T]GCAGGCACAGTGGAA | 221178 |
rs9580870 | snp | A/G | 0.171057 | 0.237209 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107360 | TGTCCCCAGAGAAAC[A/G]AGCACTCCTCATCAC | 221178 |
rs9580871 | snp | A/G | 0.324382 | 0.238678 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107503 | CTGTTTCTCTCAGAA[A/G]ATATGAAAAGCAAAT | 221178 |
rs9580872 | snp | C/G | 0.215144 | 0.247558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107616 | CTTATATTTATATGT[C/G]TGTGAATTCCACATA | 221178 |
rs9580873 | snp | A/G | 0.324145 | 0.238752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107721 | AGACTTGGTAAGAAA[A/G]AAATGGGAGTTCCCA | 221178 |
rs9580874 | snp | C/T | 0.159292 | 0.232964 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109111 | ctatccctctccttt[C/T]cccgcaccccacaac | 221178 |
rs9580875 | snp | C/T | 0.158962 | 0.232835 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109894 | ctagaagtgaaattg[C/T]tgaatcaaaggtggc | 221178 |
rs9580876 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113141 | TAACCGGACAATGTC[C/T]ACTTTAAGTTTTAGT | 221178 |
rs9580878 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118560 | gtttattaaaacaca[C/G]atgacttaagcccca | 221178 |
rs9580879 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124018 | CCGTCCAGCTTGGCT[C/T]CAGCTAGGAAAGATT | 221178 |
rs9580881 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132361 | ATAGGGCCATCTGGA[A/C]CAAGTCCTAATTTAT | 221178 |
rs9580883 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135468 | tttgggagactgagg[C/G/T]gggcagatcacgagg | 221178 |
rs9580886 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140623 | CTTGTGCGTGTCCTT[C/T]TGAGACAGCTCTCAA | 221178 |
rs9580887 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143961 | GAAACCACAGGGCAT[A/G]TGATGAGAGGTCACA | 221178 |
rs9580888 | snp | C/T | 0.408017 | 0.193729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144805 | TCGTGCAGTACGGTA[C/T]GCTGAGCAAATCCTT | 221178 |
rs9580889 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154988 | tcagcctcccttgta[A/G]ctgggattacaggtg | 221178 |
rs9580890 | snp | A/G | 0.382473 | 0.212016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165281 | CTCAGACTGTCTCCC[A/G]CCCCAGCATGCCAGG | 221178 |
rs9580892 | snp | A/G | 0.475437 | 0.108066 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170687 | GCCAATCAGTCTGGC[A/G]TAAAAAGATCATTAT | 221178 |
rs9580894 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192881 | GAGGCACTTCCAGAG[C/T]CCAGCAGGTGGTCCT | 221178 |
rs9580895 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193568 | GAGAAACCAGTTGAG[C/T]CTGGAACCTTGGGAA | 221178 |
rs9580896 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199249 | TCCAGCACCCACGCC[A/G]GCTGCAATCCATGTT | 221178 |
rs9580897 | snp | A/G | 0.158632 | 0.232706 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206881 | tgggcaacgagtgaa[A/G]ctctgtctcaaaaaa | 221178 |
rs9580898 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221434 | TGAGACATGTAGGCT[A/C]TCACTTGAAGGCTAA | 221178 |
rs9580900 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229346 | GGCACATGTTTCTAG[C/T]TGAGTTGGGACCCTG | 221178 |
rs9580901 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230126 | GAGAGAACAGGAAGT[A/C]ATGTAATTTGGTTTG | 221178 |
rs9580902 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231519 | tgttgatggagatgg[A/G]ttgtttctgcctttt | 221178 |
rs9580903 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239572 | tggtggtgtgcacct[C/T]tagtcccagctactt | 221178 |
rs9580904 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241440 | ACGGCATTACTCAGC[A/G]AAACGCAGAGTGTTT | 221178 |
rs9580905 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24241444 | CATTACTCAGCGAAA[C/T]GCAGAGTGTTTTGCC | 221178 |
rs9580906 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245965 | ATCCCGAGTCCTGCC[C/T]GCTGCTGTCTACTGA | 221178 |
rs9580907 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247523 | ctccttctgtcaccc[A/G]ggctggagtgcagtg | 221178 |
rs9580908 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262403 | GTTTGATCAGATCAC[A/G]CCACGTTTCTGTTTT | 221178 |
rs9580909 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265458 | GGACATTGGCCTGAA[C/T]AACTGATAGCAAATG | 221178 |
rs9580911 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278873 | CACATGCTGTTTTTC[C/T]TTCCTTCCTTCCTTC | 221178 |
rs9580912 | snp | C/T | 0.444444 | 0.157135 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278877 | TGCTGTTTTTCTTTC[C/T]TTCCTTCCTTCCTTC | 221178 |
rs9580913 | snp | C/T | 0.00243025 | 0.0347738 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24286375 | TAAGGAAGCCTGGTT[C/T]CCCGCGAGCTTCGTC | 221178 |
rs9580914 | snp | A/C/G | 0.00399236 | 0.0445005 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286814 | CCAGCAGCACCCCCA[A/C/G]TGAGGAGCAGGACGA | 221178 |
rs9580915 | snp | C/T | 0.0108435 | 0.0728299 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286947 | CCTCAGGGACATCTG[C/T]GAGGTGGGACGCCAG | 221178 |
rs9580916 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287511 | CAGGACCTAATTCCT[A/G]AGATTATTTGAAAAG | 221178 |
rs9580917 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288302 | GAACTATTACATTAT[A/G]TTGTTTTCCTGTTAA | 221178 |
rs9580918 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288391 | AATGTCATGATAACT[A/C]TTTTTGAGTTAGCTG | 221178 |
rs9580919 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291762 | tatttttttattttt[A/T]tttttgagacggagt | 221178 |
rs9580920 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293022 | aaaaaaaaaaaaaaa[A/T]GGCGAGGGTGTGGGG | 221178 |
rs9580921 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293476 | CACACCTCACTCTTC[A/G]GTAGTTGATTTTCTT | 221178 |
rs9580922 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296331 | CTCCAAAAAATATTG[C/T]GTGTGACTGGGATTA | 221178 |
rs9580923 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296374 | ATCTTATTTAACAAA[A/G]GCCATTGTCATACCA | 221178 |
rs9580924 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296954 | TCTGAGAAAGATTCT[A/G]TGTTAGGAGTCTCTT | 221178 |
rs9580925 | snp | A/G | 0.496842 | 0.0396107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299200 | AGTGTTTGGATTCCC[A/G]AAGACGGCACTATTT | 221178 |
rs9580926 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300703 | CATAGGAAACCTTCA[C/G]AGGGGCTGCTGGAGG | 221178 |
rs9580927 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302093 | TGACTGTCAGTCTGG[C/T]TCAGATTCTGCCACT | 221178 |
rs9580928 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302131 | GCACGTCCTGGCATT[C/T]AGTTTCTTTCCCTGT | 221178 |
rs9580929 | snp | A/G | 0.495671 | 0.0463237 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303013 | AAACACCCGTGACCC[A/G]CTATGAGATGGCCCA | 221178 |
rs9580930 | snp | A/G | 0.488916 | 0.0736153 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303304 | CTACAGCTGCCGTGG[A/G]GCTGACCACGGTGTT | 221178 |
rs9580931 | snp | C/G | 0.49168 | 0.063958 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303412 | CAAAGTGGAGAGAAA[C/G]AAGATGCATCTGTCA | 221178 |
rs9634393 | snp | A/C | 0.341235 | 0.232758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114785 | CTCTTGTCTCAGCCT[A/C]CCGAGTAGCTGAAAA | 221178 |
rs9634394 | snp | C/T | 0 | 0 | stop-gained, intron-variant | SPATA13 | GRCh38.p7 | 13:24223311 | AAAGGAATTCAGAGC[C/T]GAGAGGGGTCAAATG | 221178 |
rs9634395 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24238558 | TGTTTTGGGAATTCA[C/T]TGGGTGACACAGGAA | 221178 |
rs9669933 | snp | C/T | 0.29278 | 0.246313 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269785 | gtagagacaggacct[C/T]gctatgttgcccagg | 221178 |
rs9670766 | snp | A/G | 0.318656 | 0.240388 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209686 | GGGACACTTAGGTCA[A/G]TTGCGTATCTTGGCT | 221178 |
rs9805786 | snp | G/T | 0.458545 | 0.137872 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084217 | ATTTAAATGCGTTGG[G/T]GAGATGTGGGTGGAA | 221178 |
rs9971992 | snp | G/T | 0.475525 | 0.107882 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195577 | CCAGCAATATAAGAG[G/T]GTTCTGATTTTTCCA | 221178 |
rs10047695 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134366 | TGGAAGATTCTGGTG[C/T]GCTGCTCAGGGCATC | 221178 |
rs10047720 | snp | C/T | 0.499035 | 0.0219437 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116772 | gaagccctaccagcc[C/T]cccccccccaatgtg | 221178 |
rs10129076 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292424 | CTACCCAGGGGCGCA[A/G]GGGTCTAGGCTAAAG | 221178 |
rs10129132 | snp | C/T | 0.109461 | 0.206758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292332 | GTAGCAGTGCTTGGC[C/T]AATTCTGAGTTCTCA | 221178 |
rs10162067 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278996 | cctccctccctccct[C/T]ccttccttccttccC | 221178 |
rs10219806 | snp | C/T | 0.095934 | 0.196885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063633 | attacacagcttccc[C/T]gagcccactcaagtg | 221178 |
rs10444656 | snp | C/T | 0.44638 | 0.154709 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097462 | TGAGTGTGTGGGTGA[C/T]GACCACTTTTTCCTA | 221178 |
rs10454658 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245610 | tttttttttttttta[A/G]acaacaggtcttgct | 221178 |
rs10459340 | snp | A/G | 0.0482946 | 0.147699 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978714 | TAtttgtcttttttt[A/G]tttgtttttgagaca | 221178 |
rs10459401 | snp | C/T | 0.148661 | 0.22854 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012674 | CAACCCCCAAGTGTG[C/T]GGTGGGCGGGGTGCA | 221178 |
rs10507336 | snp | A/G | 0.341685 | 0.232581 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031661 | ATGTCAGGCACTGTA[A/G]ATGCAAAAATAGCTA | 221178 |
rs10523910 | in-del | -/CTCTCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295695 | TCTCTCTCTCTCTCT[-/CTCTCT]GTATTCATAAAAACA | 221178 |
rs10529866 | in-del | -/CACACACACACACACACACACACA | 0.350109 | 0.229081 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201032 | ATTCAGCTAGTCAGT[-/CACACACACACACACACACACACA]CACACACACACAGAG | 221178 |
rs10533629 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082827 | AAAAAAAAAAAAAAA[-/A]TAAGATCTTTGCATT | 221178 |
rs10549264 | in-del | -/AGAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065616 | TCACAAGACAGAGAG[-/AGAC]GTCCCCTAAGCCACA | 221178 |
rs10555970 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128736 | AGTCCTACCTTATTT[-/A]AAAAAAAAAAAAAAA | 221178 |
rs10557876 | in-del | -/TG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037554 | CTGGGACTACAGGTG[-/TG]CACACCACCACACCT | 221178 |
rs10566756 | in-del | -/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014897 | TTGGCACTTTCTGGA[-/T]TTTTTTTTTTTTTTT | 221178 |
rs10571334 | in-del | -/ACACACACAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24233919 | CACACACACACACAC[-/ACACACACAC]TGATAAGATTATTTC | 221178 |
rs10590370 | in-del | -/TCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063128 | CTGGACCAGGCTCCT[-/TCT]CCCAGTGCTCACCAT | 221178 |
rs10594331 | in-del | -/GT | 0.131038 | 0.219882 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037551 | TAGCTGGGACTACAG[-/GT]GTGCACACCACCACA | 221178 |
rs10608738 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202542 | TTTTTTTTTTTTTTT[-/TT]AGCTTCACTTGTACT | 221178 |
rs10616938 | in-del | -/CT | 0.495745 | 0.0459295 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132967 | GGCAACAGAGTGAGA[-/CT]CTGTCTCAAAAACAA | 221178 |
rs10622946 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198952 | AGAACTATAAAATCT[-/TT]TTTTTTTTTTTTTTA | 221178 |
rs10625714 | in-del | -/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247487 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCCT | 221178 |
rs10626783 | in-del | -/CA | 0.385932 | 0.209815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207561 | AGTACACCCGGGTTC[-/CA]GTTTCTCCACATCCC | 221178 |
rs10627896 | in-del | -/TG | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045474 | ATGCCCTAAACAAGC[-/TG]TAAGATTATTAAATT | 221178 |
rs10636364 | in-del | -/GAGTA | 0.247053 | 0.249983 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086066 | GAAGTTTCACTGTGG[-/GAGTA]GAGTAGCAGGAGAAA | 221178 |
rs10649768 | in-del | -/T/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998943 | TTTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTCTTGC | 221178 |
rs10661968 | in-del | -/TG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045475 | TGCCCTAAACAAGCT[-/TG]AAGATTATTAAATTC | 221178 |
rs10664344 | in-del | -/GTAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048468 | GATCTAGTAAACTAA[-/GTAA]TCAAGGATGAAGAGG | 221178 |
rs10676141 | in-del | -/CT | 0.499741 | 0.0113788 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074144 | CTTGAAGATCTGAAA[-/CT]CTGTCTTCATTAAAC | 221178 |
rs10691522 | in-del | -/TTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019106 | TATTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCGC | 221178 |
rs10712257 | snp | A/T | 0.140581 | 0.224783 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983657 | GTTGTTTTTTTTTTT[A/T]AAAAAACATCCAGAA | 221178 |
rs11148985 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128268 | CCCGGAGGGGTGACC[A/T]ACACGTGGGACAGGA | 221178 |
rs11148989 | snp | C/T | 0.434687 | 0.168495 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140047 | GCACGCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 221178 |
rs11149028 | snp | G/T | 0.319376 | 0.240181 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244902 | AGCAAGAGTTAAAAG[G/T]GCAGCAATTCCACTG | 221178 |
rs11149052 | snp | C/T | 0.234109 | 0.249494 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285383 | GGCTTGGCTCTGTGA[C/T]ATCTAGTACGGCTGC | 221178 |
rs11149054 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288672 | TGTGAAATGGAATTA[A/G]GGTTGGGAGAATGAT | 221178 |
rs11149055 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288690 | TTGGGAGAATGATTA[C/T]CTGAAGAGTTTGGAA | 221178 |
rs11149059 | snp | C/T | 0.425116 | 0.178422 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303307 | CAGCTGCCGTGGGGC[C/T]GACCACGGTGTTCCC | 221178 |
rs11272185 | in-del | -/TGTATGTATGTATGTG | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269359 | ATCACTTGTTTAACA[-/TGTATGTATGTATGTG]TGTATGTATGTATGT | 221178 |
rs11276937 | in-del | -/CCCACCTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24296889 | ACCTTTGAGGCCCTG[-/CCCACCTG]TGAATGGGGACAGGT | 221178 |
rs11281898 | in-del | -/ATGAAG/TGAAGA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277525 | ACAGAGTCATGAAGA[-/ATGAAG/TGAAGA]CTGGCTGAGGGATTT | 221178 |
rs11282008 | in-del | -/AGGAGACTA | 0.213635 | 0.247341 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064991 | ACTGTCACAGGCCAC[-/AGGAGACTA]AGGAGCCAGGATAAT | 221178 |
rs11282161 | in-del | -/TCATAC | 0.463451 | 0.130149 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995224 | TGTTAAAATTATTTA[-/TCATAC]TCATACTTAGCTGAT | 221178 |
rs11282320 | in-del | -/TCATGATG | 0.332568 | 0.235971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074498 | ATTGTACTCATGATG[-/TCATGATG]ACTGTCCCTTATGCA | 221178 |
rs11282550 | in-del | -/GAAGAAAG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276650 | AAGAAAGGAAGAAAG[-/GAAGAAAG]AAACAATAAAATTTA | 221178 |
rs11288795 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212297 | GAGACCCTGTTTAAG[-/A]AAAAAAAAAAAAAAA | 221178 |
rs11295105 | in-del | -/T | 0.0352966 | 0.128072 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111075 | ACCATGTATGGCTGA[-/T]TTTTTTTGTATTCTT | 221178 |
rs11321247 | in-del | -/A | 0.175213 | 0.238552 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138138 | AACCCCATCTCTTCT[-/A]AAAAAAAAAAATACA | 221178 |
rs11333086 | in-del | -/T | 0.469544 | 0.119585 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147777 | CACACCCCTAGCCCC[-/T]GGCAGACACCATTCT | 221178 |
rs11353469 | in-del | -/T | 0.324145 | 0.238752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072826 | TCTACTGTTGGCTCC[-/T]TTTTTTTTTTTTTTT | 221178 |
rs11354139 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138751 | ACCACCCCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 221178 |
rs11396232 | in-del | -/T | 0.473081 | 0.112848 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202589 | ACTTTTTTTTTTTTT[-/T]GTATTTGTAGATTTG | 221178 |
rs11411217 | in-del | -/T | 0.449726 | 0.150364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222471 | GGTATTTCCTAATTA[-/T]TTTTTTTTTCCATTT | 221178 |
rs11412529 | in-del | -/C | 0.476746 | 0.10529 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179597 | TGTACAGATTAAATG[-/C]CAAGTCCCTATTTAT | 221178 |
rs11421515 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24107238 | AAAAAAAAAAAAAAA[-/A]GCTCAAGCCTGGTTC | 221178 |
rs11448750 | in-del | -/G | 0.344592 | 0.231414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093949 | GCCTCTCCCCGTCCC[-/G]GGAGGTTAGATGTCA | 221178 |
rs11455623 | in-del | -/T | 0.494184 | 0.0536119 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058963 | TGTGTATTGTTTTTT[-/T]GTTTTGTTTTGTTTT | 221178 |
rs11483594 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24218733 | TGCGATTTTTTTTTT[-/T]AATCTCATCAGCAGT | 221178 |
rs11616239 | snp | C/T | 0.472709 | 0.11358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098662 | ggccggatgtggtgg[C/T]ttatgactgtaatcc | 221178 |
rs11616414 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103503 | aaaaaaaaaaaaaaa[A/C]aAGAAAGAAAAGAGC | 221178 |
rs11616597 | snp | A/G | 0.135484 | 0.22223 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225659 | ACTGCTTCCTGTTGC[A/G]TGTTGCAGCTGCCTG | 221178 |
rs11617302 | snp | C/T | 0.370772 | 0.218893 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231920 | ttagtgaagtgccga[C/T]tcagatcttttgctc | 221178 |
rs11617540 | snp | A/G | 0.378962 | 0.21417 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103504 | AAAAAAAAAAAAAAC[A/G]AGAAAGAAAAGAGCA | 221178 |
rs11617559 | snp | C/T | 0.4862 | 0.0819127 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178086 | CTTGAACTCCTAGAT[C/T]CCAATGATCCTCCCA | 221178 |
rs11617580 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288441 | TTTCTTCTTATCCCA[C/G]TAGCTCCTACCTAAG | 221178 |
rs11617616 | snp | A/T | 0.36955 | 0.219562 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233047 | TTTTTGTGTGTAATA[A/T]GAAGGTTCATTTTTT | 221178 |
rs11617774 | snp | G/T | 0.475259 | 0.108435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103681 | TGTATCTATATGTAT[G/T]TCTATATATTGTAAC | 221178 |
rs11618409 | snp | C/T | 0.451732 | 0.147663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186131 | CCAAATAACTGGGCA[C/T]CACAGTCCTAGCCAC | 221178 |
rs11618423 | snp | C/T | 0.45645 | 0.140991 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185580 | GACTATTGATAAGTC[C/T]TTTATATGGTCTCAT | 221178 |
rs11619017 | snp | C/T | 0.487621 | 0.0776941 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062059 | CAGAGGTGTTATGTG[C/T]GATGGAAGCGTCACT | 221178 |
rs11619283 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086450 | AGAGGGCTGCTCATA[C/G]GGAAACGTGGGCAGT | 221178 |
rs11619480 | snp | C/T | 0.482979 | 0.0906686 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169429 | TGACAAGTCGTAAGG[C/T]GTGAGTAGACTGGTT | 221178 |
rs11620172 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089033 | GGGACACGTTCACAG[A/G]TGGCTTTGAAAAGTA | 221178 |
rs11838753 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170287 | ATCAAACCCCACACA[A/C]CAATTATTCTAAAGC | 221178 |
rs11838928 | snp | G/T | 0.349671 | 0.229272 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066938 | CAGAGGCCTGGGGTT[G/T]CCATTTGCAAGATAA | 221178 |
rs11839477 | snp | C/T | 0.136166 | 0.22258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046473 | aatttattgtaggga[C/T]ggagtcttgctatgt | 221178 |
rs11839907 | snp | A/G | 0.117537 | 0.212022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047978 | gcgtcaatgtctgac[A/G]tcccagggtaggaga | 221178 |
rs11839932 | snp | A/G | 0.225301 | 0.248777 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173441 | gtgggcaatcatgtc[A/G]tgtacaaatggaatg | 221178 |
rs11840533 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003851 | ACAATATTAGAGACG[C/T]GGGAAAAAACACAAT | 221178 |
rs11840635 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109546 | TGTTTTCCCTTACTG[A/T]CATTTGGAGGTCTTA | 221178 |
rs11840813 | snp | A/C | 0.103794 | 0.20279 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144009 | AGGGTTGGCCAGAAA[A/C]ACTCAAAGCACGTAG | 221178 |
rs11841187 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040871 | GGTTGGCCCAACACA[A/G]GCAGCTTTTGCTCAG | 221178 |
rs11841500 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041067 | ACAAATACAGCAAAA[C/T]CACAATGCCTGCCTG | 221178 |
rs11842218 | snp | A/T | 0.231482 | 0.249313 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059153 | ATTTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT | 221178 |
rs11842597 | snp | C/T | 0.00187793 | 0.030585 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224083 | TGCATGGGACCACTG[C/T]AACCTGCACCGTGGC | 221178 |
rs11842605 | snp | A/G | 0.406468 | 0.194981 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252500 | AATTCAATCAAAAAC[A/G]TATACCATGTTTGTA | 221178 |
rs11842607 | snp | A/G | 0.406814 | 0.194704 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252528 | GTAACAATATGCAAC[A/G]TGTACCCATATGGCA | 221178 |
rs11843284 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143847 | CTTGGAGGAACATGT[A/G]ACACTTTCTCTCTGG | 221178 |
rs11843356 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025832 | tttttttttttgaga[C/T]ggagtctcactctat | 221178 |
rs11843570 | snp | A/G | 0.416382 | 0.186593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143955 | TGCCCTGAAACCACA[A/G]GGCATATGATGAGAG | 221178 |
rs11843576 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143996 | AGAAAGGCCGCCCAG[C/G]GTTGGCCAGAAACAC | 221178 |
rs11843719 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077022 | GGGGACCCTGGGTTT[C/T]TTAACGAGCCAGTTT | 221178 |
rs11843971 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248718 | AGCCCTGGACTTAGT[C/T]CTCTTAAAGCACCTT | 221178 |
rs12017641 | snp | A/T | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110291 | AGGAGTGAGGAAGGG[A/T]GGGGAGGATGGCTCT | 221178 |
rs12017690 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137621 | aaaaattaggcaagc[A/G]tggtacgcatgcctc | 221178 |
rs12100261 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179796 | ttcatgtgcttattg[A/G]ctatttggatatctt | 221178 |
rs12184884 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113422 | agcctggccaacatg[A/G]agaaaccccatctct | 221178 |
rs12232067 | snp | G/T | 0.368324 | 0.220226 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114656 | TTTTTTGTTGTTGTT[G/T]TTTGTTGTTGTTTTT | 221178 |
rs12323145 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002667 | TGGAATAGGACTGCC[A/G]CAAGCCTCGTCCGGC | 221178 |
rs12427506 | snp | A/T | 0.317933 | 0.240593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028256 | GCATTTGAGCTAATT[A/T]ATTTTCTTCCATAGT | 221178 |
rs12427693 | snp | A/G | 0.45889 | 0.13735 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026727 | GGACTACAGGTGCCC[A/G]CCACCACGTCCAGCT | 221178 |
rs12427719 | snp | A/G | 0.266 | 0.249487 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024792 | GCCGGGTGCAGTGGC[A/G]CATGCCTGTGGCCCC | 221178 |
rs12427808 | snp | G/T | 0.306182 | 0.243605 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029508 | acaataaaaaaattt[G/T]gtatGTTATTTACAT | 221178 |
rs12427896 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24009644 | ttactatctaaagac[C/T]tagaatcaatagaaa | 221178 |
rs12427946 | snp | C/T | 0.392325 | 0.205532 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004345 | AGATACCATTTACGG[C/T]AGTGTTGACAGTTAG | 221178 |
rs12428182 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171703 | GCCTGTAAGATAATT[G/T]TGAACTTGCAGATTA | 221178 |
rs12428194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156712 | TTGAGCATTTGACCA[C/T]GTGCCAGGCAGTGAG | 221178 |
rs12428476 | snp | A/G | 0.306679 | 0.24349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029384 | ttagacaaatagtgt[A/G]aaatcaagacccaaa | 221178 |
rs12428492 | snp | A/G | 0.306182 | 0.243605 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029513 | aaaaaaattttgtat[A/G]TTATTTACATAAAAT | 221178 |
rs12428504 | snp | A/G | 0.340108 | 0.233197 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029655 | atttcaggggtacaa[A/G]tgcagctttgttaaa | 221178 |
rs12429015 | snp | A/G | 0.394904 | 0.203722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004708 | GGGCTGAAAATTTAC[A/G]TTCCATACGATTTAT | 221178 |
rs12429315 | snp | C/G | 0.350327 | 0.228986 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002239 | ATTCAATAGCTCACT[C/G]TAACACTATGCCTGT | 221178 |
rs12429462 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048082 | acgcctcccacatta[G/T]ggagagtgagtcttt | 221178 |
rs12429718 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079070 | agagggcttcttgga[A/G]gaggtggtactgatc | 221178 |
rs12429878 | snp | C/T | 0.472335 | 0.114312 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986880 | AGATTGGAAACATCA[C/T]GGGATCTCGTTGTGC | 221178 |
rs12429885 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24280604 | ATTCCTGCTGCTTTA[A/G]GCATTAGACACCCAG | 221178 |
rs12429956 | snp | A/G | 0.394904 | 0.203722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004693 | TGCTCCATACACACA[A/G]GGCTGAAAATTTACA | 221178 |
rs12429964 | snp | A/G | 0.395818 | 0.203069 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004788 | CTACAGTGACAGTAG[A/G]CTAATAATAGTAAGA | 221178 |
rs12430045 | snp | C/T | 0.317451 | 0.240729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021962 | gtaatctgcctgcct[C/T]ggcctcccaaagtgc | 221178 |
rs12430243 | snp | A/C | 0.465263 | 0.127129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019078 | AGTTATATGATTCTT[A/C]TTATTATTATTATTA | 221178 |
rs12430246 | snp | A/C | 0.436408 | 0.16659 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019084 | ATGATTCTTATTATT[A/C]TTATTATTATTTTTT | 221178 |
rs12430286 | snp | C/T | 0.316968 | 0.240864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028428 | GGTTGTTAGTTTCTC[C/T]TAGTACTTTACAGAT | 221178 |
rs12430530 | snp | A/G | 0.334908 | 0.23514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290919 | GGCACAGGTGAGAGC[A/G]CTGCTGCCATTACCC | 221178 |
rs12430549 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145472 | GATTGTTCTCAGTTC[A/G]TGTGAGTCCACAGAG | 221178 |
rs12430567 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300144 | CTTCACACAGACATT[C/T]TGCATTCTCATGAGC | 221178 |
rs12430586 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029583 | AACATATAGACTGTT[C/T]TGTAGAGCATTTTTG | 221178 |
rs12430935 | snp | A/T | 0.341909 | 0.232492 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026494 | GGTAAGATGGAATTA[A/T]TTGGCCCTTTATGTT | 221178 |
rs12583123 | snp | A/C | 0.380333 | 0.213338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103014 | ATCCCGTTTTCCCAG[A/C]ACCTTTTGTTGAAGA | 221178 |
rs12584178 | snp | A/G | 0.307423 | 0.243316 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979029 | ATTGGTCTATCTTCA[A/G]GTTCACCAATGAATT | 221178 |
rs12584287 | snp | C/T | 0.308166 | 0.243139 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983626 | CCATTTATTTTTACA[C/T]TAGTATATTCTGTTG | 221178 |
rs12584323 | snp | A/G | 0.398894 | 0.200825 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302514 | GAGAACTTGGACTTG[A/G]AGTCTCAGCATTTTT | 221178 |
rs12584764 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24178901 | attttcatcccctcc[A/G]aaaggaaaccctgga | 221178 |
rs12584822 | snp | C/T | 0.190519 | 0.242821 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061205 | cagaatgactgttac[C/T]gaactgtcaaaaata | 221178 |
rs12584863 | snp | A/G | 0.296364 | 0.245663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234693 | CTGGGGCAGACTTCA[A/G]GGAGTCAACTGGTGC | 221178 |
rs12584972 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118772 | GCCTAGCACATAATC[A/T]CCTCTCAATAGCAAA | 221178 |
rs12585023 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275788 | aaaatacaaaaatta[A/G]ctggatgtgatggca | 221178 |
rs12585032 | snp | C/T | 0.372391 | 0.217992 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027283 | gggattacaggcgtg[C/T]gccaccacacccagc | 221178 |
rs12585225 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019087 | ATTCTTATTATTAtt[A/C]ttattattttttttt | 221178 |
rs12585481 | snp | A/G | 0.21875 | 0.248039 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115756 | agtgggttgtgatca[A/G]ggtatcagcggaggc | 221178 |
rs12585569 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157990 | ATGAATGTAAACAAC[A/G]TGGCATAAGTGTCCA | 221178 |
rs12585790 | snp | A/G | 0.449853 | 0.150196 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189144 | agcccatggatcaag[A/G]agtaattttgactct | 221178 |
rs12585877 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277611 | ctatcctggttcgga[A/C]ccagcccctgtatag | 221178 |
rs12585910 | snp | C/T | 0.402277 | 0.198272 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302213 | AGAGAGACTGTGTCA[C/T]GCTCCACACGGAGTA | 221178 |
rs12585932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019190 | gcctcccgggttcac[A/G]ccattctcctgcctc | 221178 |
rs12586059 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184977 | ATGGGTCATTCCTCA[A/G]GAAAGTGCGGGTGCC | 221178 |
rs12857288 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282710 | TAGCCCAGCCCTCAT[C/T]GTGCGGGACACCATC | 221178 |
rs12860170 | snp | A/G | 0.425894 | 0.177655 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221597 | CTGAGGGGAAGGGAT[A/G]GACACAGGTGTGTGG | 221178 |
rs12862898 | snp | G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994849 | AAGCCCTACATTTTA[G/T]GCCAAAAGGCAGATT | 221178 |
rs12863941 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161597 | AAGCCCGCGCTGCTG[C/T]CAGCGTCAGGGGGAG | 221178 |
rs12864662 | snp | A/G | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052134 | CTTAACGCAATTCCA[A/G]ATGGAAGAAAGGGAG | 221178 |
rs12864809 | snp | C/T | 0.148326 | 0.228391 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994832 | GAAAATGGCTTGTAA[C/T]CAAGCCCTACATTTT | 221178 |
rs12865020 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24020973 | ttgaacccaggaggc[A/G]gtggttgcacagggc | 221178 |
rs12865045 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021016 | actgcactccagcct[A/G]tgtgacagattgaga | 221178 |
rs12865055 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021028 | cctgtgtgacagatt[A/G]agactccatctcaat | 221178 |
rs12865245 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226908 | TCCCCTGGGCAGCCA[C/G]AGAAGTGAGACTGCA | 221178 |
rs12865567 | snp | A/C | 0.14665 | 0.227637 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295840 | actattattataccc[A/C]tttaacagatgggaa | 221178 |
rs12866210 | snp | A/G | 0.089084 | 0.191327 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292490 | TGCCCCTGACACAAA[A/G]TCTTTAACTGCACCT | 221178 |
rs12866223 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292519 | CTGCAGCTCTGGAGA[C/G]GGTCATCTCAAAGGG | 221178 |
rs12866680 | snp | C/T | 0.473266 | 0.112482 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166957 | ACACATACATTCAGA[C/T]CGTAGCAGTTCCCAT | 221178 |
rs12866690 | snp | A/C | 0.0158469 | 0.0875917 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306537 | CCATAATAACCTAAT[A/C]TGCAAATTGTTCTAT | 221178 |
rs12866835 | snp | A/G | 0.215747 | 0.247642 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118395 | AGTTACTCCTGGCAC[A/G]TGTGGATTATTTATA | 221178 |
rs12866852 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246413 | AGGAAAAAAACGTTT[A/C]CTCTACACTCTTTGA | 221178 |
rs12866927 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24226909 | CCCCTGGGCAGCCAG[A/T]GAAGTGAGACTGCAT | 221178 |
rs12866968 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291750 | TCTTTATTTTTTTAT[A/T]TTTTTATTTTTTTTT | 221178 |
rs12867597 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236078 | agtgaggggtggggt[C/T]gggcctgcagctggg | 221178 |
rs12867797 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292387 | CATAGGGCAACTGCT[A/G]TGTGCCAGGCTCCAA | 221178 |
rs12868188 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271041 | ctctctctctctctc[A/T]ctctctctctctctc | 221178 |
rs12868205 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271059 | ctctctctctctctc[A/T]ctctctctctttctc | 221178 |
rs12868327 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191502 | CTATACATTGCtttc[C/T]ttttttttttttttt | 221178 |
rs12870498 | snp | A/C | 0.191147 | 0.242974 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274967 | TCTCACCTCCCTTTC[A/C]TTTAACAGAACACCT | 221178 |
rs12870625 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24020975 | gaacccaggaggcgg[A/T]ggttgcacagggcct | 221178 |
rs12870646 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021017 | ctgcactccagcctg[G/T]gtgacagattgagac | 221178 |
rs12870654 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021026 | agcctgtgtgacaga[G/T]tgagactccatctca | 221178 |
rs12870966 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275283 | ACTGGGGAAGGACCA[A/G]TGCAGCCCCAGGAAT | 221178 |
rs12870973 | snp | C/T | 0.37955 | 0.213815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219118 | TAGTTCTGTTCTCTT[C/T]CTATCTCTGGCAGAG | 221178 |
rs12871319 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246451 | CTTAAGTCCTGTGAA[A/T]TTTAAggcctgtgaa | 221178 |
rs12871737 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293690 | CTGGAGGCCTCTTTG[A/G]GGGCTCTGTGCCCAT | 221178 |
rs12871948 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189590 | actatgtatgtaata[C/T]aaatataaatataAA | 221178 |
rs12872112 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271043 | ctctctctctctcac[A/T]ctctctctctctctc | 221178 |
rs12872120 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271061 | ctctctctctctcac[A/T]ctctctctttctctG | 221178 |
rs12872216 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271070 | tctcactctctctct[C/T]tctctGCTGCTTGTC | 221178 |
rs12872458 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272524 | CTTTGAGAGCTCTGA[A/G]AGGGCAGGGGGCAGG | 221178 |
rs12872503 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189628 | TTAATTTATtatata[A/T]atatatatatttata | 221178 |
rs12872507 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189633 | TTATtatataaatat[A/T]tatatttatatatat | 221178 |
rs12872627 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189690 | tatatatttatatat[A/T]atatataatatatta | 221178 |
rs12872637 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080223 | CATGACCGTATGTCA[A/G]AACAGCAGCGCCTAG | 221178 |
rs12874010 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272530 | GAGCTCTGAGAGGGC[A/C]GGGGGCAGGGGAGGG | 221178 |
rs12875066 | snp | A/G | 0.140919 | 0.224948 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107200 | GCAAGATGATCACAC[A/G]GTGGCTGGGTACTCA | 221178 |
rs12875385 | snp | A/G | 0.478188 | 0.10213 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290351 | GAGGCCCTGCTCCCC[A/G]CCTTCCAGGATGAGC | 221178 |
rs12875950 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063656 | ctcaagtgggggcgg[C/T]tccttctcccacatc | 221178 |
rs12876068 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189539 | ttgcatacatattta[A/T]atttaaatatatagt | 221178 |
rs12876136 | snp | G/T | 0.252421 | 0.249988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197996 | CCTGTTACCTCGTGT[G/T]TGTTTGTTTGTTTGT | 221178 |
rs12876424 | snp | C/T | 0.245631 | 0.249962 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299801 | CTTCCCCACACCCTG[C/T]GAAGCCAAGGGTTGC | 221178 |
rs12876515 | snp | C/G | 0.477684 | 0.103247 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169458 | TTTCAAAATCAGTCT[C/G]GGTTCTATTTGTTGT | 221178 |
rs12876600 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24056830 | GCCACAGGTCCAATT[C/T]TGCCCCTCACATCGT | 221178 |
rs13313271 | snp | C/T | 0.296873 | 0.245566 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282190 | GAGTCTGGGGCTGGA[C/T]GTGTGTCTGCCGAGC | 221178 |
rs13378215 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264992 | CGCTGAGAGCACATA[C/T]TCGCTGGTTTTGTGT | 221178 |
rs13378382 | snp | C/T | 0.114387 | 0.210022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258191 | agtgagcctacattg[C/T]gccatggcactccag | 221178 |
rs13378404 | snp | A/T | 0.350546 | 0.22889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048006 | agacagatgtccttt[A/T]tgccaaggtcactct | 221178 |
rs13378562 | snp | A/G | 0.391024 | 0.206427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108751 | TCACCTTTCAAGCCT[A/G]GAGGCCCCGAGCCCA | 221178 |
rs17079683 | snp | C/T | 0.308414 | 0.24308 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982847 | ATTGCAAACCAGGTA[C/T]ACGTGTGAGCTTCGG | 221178 |
rs17079684 | snp | A/G | 0.302184 | 0.244493 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982861 | ACACGTGTGAGCTTC[A/G]GGAGGCTGGGTCTCC | 221178 |
rs17079704 | snp | A/G | 0.309154 | 0.242901 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993146 | TGAACCTGCTGTGGC[A/G]AAGGTCGTGGACAGA | 221178 |
rs17079726 | snp | C/G | 0.286564 | 0.247312 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001231 | TACAAGAACACGGGG[C/G]AAAGTAACAGTGTTA | 221178 |
rs17079728 | snp | A/G | 0.474813 | 0.109357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001706 | TGGCAGGGATGTTCA[A/G]TGATGGCCGTGGATA | 221178 |
rs17079751 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017165 | GAGTTACGAATAGAG[A/G]ACAAATCGCCAAAAT | 221178 |
rs17079752 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018338 | GAAATGTTGCAAAAG[A/G]TCGTTTTTTCCATCT | 221178 |
rs17079755 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018651 | GCTTGTTTGATGTTT[C/T]AGCAGAGGGTTACTT | 221178 |
rs17079760 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018791 | TTTGTGAGAAGAATT[A/T]CATTACAGCATTTAG | 221178 |
rs17079762 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019060 | CTAAAGAAGGGGCTC[C/G]TAAGTTATATGATTC | 221178 |
rs17079770 | snp | C/G | 0.0737376 | 0.17729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020528 | AGGGAGCTGTTGAAC[C/G]TTAAACGAATTGTAT | 221178 |
rs17079773 | snp | C/T | 0.315516 | 0.241263 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024245 | ATCCATGGTTGTATG[C/T]GCTCTAAGATTCTTC | 221178 |
rs17079787 | snp | A/C | 0.339656 | 0.233371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029390 | AAATAGTGTGAAATC[A/C]AGACCCAAATCCATG | 221178 |
rs17079798 | snp | A/C | 0.0437281 | 0.141251 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034371 | AATGAGGTAGGAGAC[A/C]AAATTTTCCATCAAA | 221178 |
rs17079801 | snp | A/G | 0.0763149 | 0.179815 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034485 | TAGAGAAAGTGATCA[A/G]TTCAAGCAGTGTCTT | 221178 |
rs17079842 | snp | A/G | 0.250168 | 0.25 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054133 | AAGCCCACAAAGAGG[A/G]GTCAGGTCAAGGACA | 221178 |
rs17079844 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055128 | GCTTTACATATATGG[C/T]ACAGAGCGATCAGCC | 221178 |
rs17079849 | snp | A/G | 0.32768 | 0.237625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056827 | CGGGCCACAGGTCCA[A/G]TTCTGCCCCTCACAT | 221178 |
rs17079863 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059590 | ATATGCTGAGGACAG[A/G]TACTTTCATTTCCAT | 221178 |
rs17079928 | snp | A/G | 0.335101 | 0.23507 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080089 | GAGAAGTGAGAAAGT[A/G]AACTGTGAATTATGA | 221178 |
rs17080016 | snp | A/C | 0.43598 | 0.167067 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103031 | CCTTTTGTTGAAGAG[A/C]TGAGTTAAACAATTT | 221178 |
rs17080021 | snp | A/G | 0.462582 | 0.131564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103168 | AATAGTTCTGAATAC[A/G]TCAAAATGGGAAATG | 221178 |
rs17080036 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104538 | GGATAGATACAAGGC[A/G]TCCCTTAGAGACAAG | 221178 |
rs17080043 | snp | C/T | 0.153 | 0.230415 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107301 | CAGTCAGTTATGTGG[C/T]CATGGCAGTGAAAAT | 221178 |
rs17080048 | snp | A/G | 0.155987 | 0.23165 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107452 | CCCAAGGCCCTAGGA[A/G]GGAATAAAAGCAAAT | 221178 |
rs17080053 | snp | A/G | 0.1652 | 0.235179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108371 | TCTTGTTCTCTCAGT[A/G]TTGAACTTAACCCCT | 221178 |
rs17080058 | snp | A/G | 0.164546 | 0.234942 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110181 | GTGGGAGCAGTAAAA[A/G]CTGGAGCACACAGAA | 221178 |
rs17080064 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112251 | GGCATTGTAGCAAAG[A/C]TGTTTGGTTTGACCT | 221178 |
rs17080078 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113238 | GTTATTTAATATCCT[A/C]GGCAAAAGTTACTTT | 221178 |
rs17080092 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122655 | CTGTATATCACTTCA[A/G]GATACTTGGTGACAG | 221178 |
rs17080130 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140345 | AATCAGTTCATAGTT[C/T]GTTGCCCCAGCAGAC | 221178 |
rs17080197 | snp | A/C/G | 0.395608 | 0.23183 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147180 | AATTGTTTCAAGAAG[A/C/G]CTACTCTGATTAATT | 221178 |
rs17080288 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165162 | AAAGGACCTGACTTC[C/T]TGGTGAGCAATCACT | 221178 |
rs17080334 | snp | C/T | 0.116838 | 0.211584 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187014 | CCAACAAAGAGACTT[C/T]TCTTAATCCTTTTCC | 221178 |
rs17080336 | snp | C/G | 0.121022 | 0.21416 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187308 | AGATGAAGAAACTAC[C/G]CTTCTGGTTGTCTGG | 221178 |
rs17080360 | snp | C/T | 0.124144 | 0.21601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200113 | AGACTTGTACAAACC[C/T]CTTCAACGGGCATTT | 221178 |
rs17080364 | snp | C/T | 0.084364 | 0.187256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200197 | TTTAGATGTGGGAAC[C/T]GAGCTCAGAGTAGCT | 221178 |
rs17080389 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204265 | TTATCCACATTTTTC[A/C]TTTTGCAGATGAAAA | 221178 |
rs17080413 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209168 | CTGTACTCAGGACAA[G/T]CCGATTTCAGGAATT | 221178 |
rs17080418 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209417 | AGACAGCTCTTGCCA[A/G]GGTTATTTGATGAAA | 221178 |
rs17080422 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211784 | GCTCCCATGACCTTT[A/T]GAGTAAACCCCAATC | 221178 |
rs17080436 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218073 | CCTGCTGGAGGGAAA[C/G]GCGTCCTGTATTAGG | 221178 |
rs17080441 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219625 | AGGCAGCCATATAAA[A/G]CTATCATTATAATCC | 221178 |
rs17080449 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220277 | GGGCCCTTGTTTCCT[C/T]CTTGGTTATAAAAGG | 221178 |
rs17080450 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220410 | ACCATTACTACTAAT[A/G]TCAGTGCCTGTGAAC | 221178 |
rs17080452 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220564 | ACTTTGCAACTGGTT[A/G]CAGGCTTCATATCCA | 221178 |
rs17080462 | snp | C/T | 0.0473439 | 0.146392 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224195 | CTGGGCGGTGGAAAG[C/T]GACAGTTCCTGCACT | 221178 |
rs17080494 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241049 | ACATGCATGTCACCC[A/C]ATTCCGTAGTAATTA | 221178 |
rs17080513 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243774 | TCACCTTGACCCCTG[C/T]ATGTGAATTCTTTTG | 221178 |
rs17080518 | snp | A/G | 0.247337 | 0.249986 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245220 | GTTCCAAGTAGAATC[A/G]CAACCAAACTACATT | 221178 |
rs17080529 | snp | A/C/G | 0.0107334 | 0.0725574 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250455 | TTAATTAAAGACCCT[A/C/G]TCTTGGAGAAGTGTA | 221178 |
rs17080537 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251616 | GGAGAAACCATTTCA[C/T]GTCTGTGAGTGGCTT | 221178 |
rs17080547 | snp | C/T | 0.106278 | 0.204558 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252899 | AGACTGGCCATGGCA[C/T]TGTCCCAGGAGCTAG | 221178 |
rs17080569 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260853 | CAGTTGATCGTACAC[A/G]GGGAGCCTTGTCCTA | 221178 |
rs17080572 | snp | G/T | 0.155325 | 0.23138 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265436 | GCACTCGATGATTTA[G/T]GGGAATGGACATTGG | 221178 |
rs17080580 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271483 | TACTGCTTTGTGCCT[C/T]ATCTCCCGCTTTCTT | 221178 |
rs17080581 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271536 | TCTATTTGTCTATTC[C/T]GTGAGTATTGGACTA | 221178 |
rs17080598 | snp | C/T | 0.151001 | 0.229563 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291547 | TACCCACCGGGGTGC[C/T]GACTCTCTGGTCTTC | 221178 |
rs17080600 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291673 | TTCTTGTTACTCACA[C/G]TTCTGTTGTTTGGAT | 221178 |
rs17080603 | snp | A/G | 0.170408 | 0.236992 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292166 | ACCCTTTGTTTCCTT[A/G]ATAGCCAACCATCAT | 221178 |
rs17080605 | snp | A/C/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293956 | GCTGTAAGTTGCCAC[A/C/G]GGAAAGCGGAAAATA | 221178 |
rs17080644 | snp | C/T | 0.0279526 | 0.114869 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306134 | AGATGAAAACCGATG[C/T]CATTCTTATTCAGAA | 221178 |
rs17348918 | snp | A/G | 0.0450888 | 0.143218 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987081 | CCCCATAGGCAGTGG[A/G]TTGATATTTTAAATG | 221178 |
rs17349638 | snp | C/G | 0.24019 | 0.249807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016265 | GAGTGCTCCATCCTC[C/G]AGGACGTGGCCCTGG | 221178 |
rs17349764 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018226 | AAATGTGCACGTGTT[A/C]ATAAATATGACATAC | 221178 |
rs17350036 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023353 | TTAAGGCATAGCTCA[A/G]TAAATTCATTTCTCT | 221178 |
rs17350335 | snp | C/T | 0.306431 | 0.243548 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033245 | ATAGAATTTCAAAAA[C/T]CTAATAAAAATGAAA | 221178 |
rs17350384 | snp | C/T | 0.298651 | 0.24522 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033386 | TCTGTTCTTGATGGC[C/T]AGACCCTCGTGGCAT | 221178 |
rs17352099 | snp | C/G | 0.172674 | 0.237741 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071870 | TTGAGCAAGATGATT[C/G]TCCCCGTGTGCACTT | 221178 |
rs17352779 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093404 | TTTTTAAAAGAGGAC[A/G]TATGGTTAGTGATCT | 221178 |
rs17353284 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104406 | GGTTTTACAATTCTC[A/G]AGGCAGGCATAAATC | 221178 |
rs17354429 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120208 | CCTCTGAAAAAAAAA[C/T]CAGGATTCTACTACT | 221178 |
rs17362866 | snp | C/T | 0.165527 | 0.235296 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184084 | TGTGGAGGAGAGCGC[C/T]AAGGGACAGTAACAG | 221178 |
rs17364679 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209366 | AACTAGATTGCTGCA[C/T]TTAAAAGTATGGGGT | 221178 |
rs17364832 | snp | G/T | 0.317692 | 0.240661 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212777 | GCTTTGTTTGGTGGA[G/T]AGGCAGGCTCAGCCT | 221178 |
rs17364874 | snp | A/G | 0.463343 | 0.130326 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212867 | CCTGAAGTTGCTGCC[A/G]TTGGGAGAAACCACA | 221178 |
rs17366913 | snp | C/G | 0.106633 | 0.204807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257044 | AGCCTACCTAAGCTC[C/G]TAATTTTTTTGTACT | 221178 |
rs17367047 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258903 | TCTTCCACTACTCAG[A/G]TCCACGTCAGGAGCT | 221178 |
rs17367130 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262881 | CCCAGAGCACTTGGA[A/G]TCTATATGGAATAAT | 221178 |
rs17380388 | snp | C/T | 0.067446 | 0.170804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283989 | TTAACTTTGGAGTAA[C/T]GTAGACATTTTCTAA | 221178 |
rs17380970 | snp | G/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305925 | CCTGGAGCAGTAGAT[G/T]TCTTTGTCTTTGGCC | 221178 |
rs17426978 | snp | G/T | 0.29432 | 0.24604 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984096 | TAATTGGAACGTGTG[G/T]CAAGAACTCCAATTG | 221178 |
rs17427444 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990762 | CACCCAGAACCTAAC[A/T]TATTGATTGCTCATA | 221178 |
rs17428490 | snp | A/C | 0.317451 | 0.240729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028709 | ATAGAATTCCAATTG[A/C]ATGTTTGTCCGTTCT | 221178 |
rs17428693 | snp | C/T | 0.309648 | 0.24278 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033535 | TGACCTGGAAGAAGA[C/T]CCTGAGGAGAACCCG | 221178 |
rs17429538 | snp | A/G | 0.106278 | 0.204558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053479 | GAAATTGAGCAAGCC[A/G]TTCTTACCTGGGATC | 221178 |
rs17429748 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057454 | CCCTCAGGGAAGCCA[A/G]TGTTGACAGGGCATT | 221178 |
rs17429818 | snp | C/T | 0.232359 | 0.249377 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058538 | GGGCTACACATTACT[C/T]AGAATAATTGATTAC | 221178 |
rs17456768 | snp | C/T | 0.469937 | 0.118861 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097774 | GCCAAAGGTATGCAC[C/T]GGAAAGCATGGTACA | 221178 |
rs17456859 | snp | A/G | 0.110872 | 0.20771 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101273 | TAAAGTCCGTATACC[A/G]TTTCATCATACAGAT | 221178 |
rs17457116 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105523 | CCAAGCACAATGAGA[A/G]AGCCTGATAAATAAA | 221178 |
rs17458394 | snp | A/G | 0.184521 | 0.241273 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122707 | CTGTTACATAATTAC[A/G]AAGGAGGAGCATCAT | 221178 |
rs17462267 | snp | A/C | 0.305934 | 0.243663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212887 | GAGAAACCACAGTAA[A/C]CAACAGTCAAACAAA | 221178 |
rs17462295 | snp | A/C | 0.316968 | 0.240864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213893 | TACAGAACATTTTAC[A/C]TTCTGGTATTTATTA | 221178 |
rs17463556 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243110 | ATTTGTGATATTGTC[G/T]GATTACAGACCTTTT | 221178 |
rs17463918 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250835 | CTGAAGCAAATTGTC[A/G]CGCATTTTAACTCAG | 221178 |
rs17464453 | snp | A/G | 0.155325 | 0.23138 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260698 | CAGCTTGGAAAAAAT[A/G]GAAAAATCGAGGAGT | 221178 |
rs17464589 | snp | A/G | 0.395453 | 0.203331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265299 | AGTTTGTGCTAGGAC[A/G]TGCCATGCCCTGTGT | 221178 |
rs17464792 | snp | A/G | 0.0165986 | 0.0895757 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270841 | GCTCTGAAGGTTGCC[A/G]TTTTCCAAACAGAAG | 221178 |
rs28372314 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233882 | ACAGAACTTTATACA[A/C/T]TTAAACACACACACA | 221178 |
rs28378618 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065619 | CAAGACAGAGAGAGA[C/T]GTCCCCTAAGCCACA | 221178 |
rs28380348 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197893 | GGCTGATTTTTCTCC[G/T]AGGATGAAGTCCCCC | 221178 |
rs28414941 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064217 | AGCTCACAGTACGTC[A/G]GTGTAACAACAGACA | 221178 |
rs28427412 | snp | G/T | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134779 | TTTATGGCCTCAGGA[G/T]AGCTTCACTCGTTGT | 221178 |
rs28436594 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146925 | TAAAAAATCTCATTC[A/G]GGCATGATTTTTTTT | 221178 |
rs28479328 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134780 | TTATGGCCTCAGGAG[A/G]GCTTCACTCGTTGTT | 221178 |
rs28489922 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042480 | TGAAGCCATTGGTGC[C/T]GATCCTCACGAGTCA | 221178 |
rs28493022 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059474 | CTGTATTGAAAAGAC[A/G]GAGATTTGGCACTGC | 221178 |
rs28545144 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134482 | ATGCCGAGAGCAGCA[C/T]ATCTCTTTTTGGCAG | 221178 |
rs28560407 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201089 | GGATTTTGATTGGAG[G/T]TATTTTTGAATCTGG | 221178 |
rs28564264 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291773 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGTTCTGTC | 221178 |
rs28564791 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24209392 | GGGGTAAGGGAATTA[A/G]GAGATGAAAAGACAG | 221178 |
rs28617742 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140756 | TGAACCCATGAATTC[G/T]GGGTTTTCTAACTTC | 221178 |
rs28623748 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24061900 | AATTAAAAAAAAAAA[A/G]GAAAAAAACTGAGGC | 221178 |
rs28624140 | snp | A/G | | | missense | SPATA13 | GRCh38.p7 | 13:24290823 | CTCACACCAGTGCAG[A/G]AGATCTGCAAATACC | 221178 |
rs28626406 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154976 | GATTCTCATGCCTCA[G/T]CCTCCCTTGTAGCTG | 221178 |
rs28638389 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099355 | TAAAGTATCCTGTCC[C/T]GTCCAACAAGTTAGT | 221178 |
rs28649746 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291997 | TCCTGACCTCATGAT[A/C]CACCCGCCTCGGCCT | 221178 |
rs28683017 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24265050 | AAGCAGTTGCTTTGA[A/G]GGCATGAAGAGAGGC | 221178 |
rs28699143 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24061901 | ATTAAAAAAAAAAAA[A/G]AAAAAAACTGAGGCT | 221178 |
rs28702614 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291782 | TGAGACGGAGTCTCG[C/T]TCTGTCGCCCAGGCC | 221178 |
rs28787104 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190288 | ATTATATATAATATA[A/T]AATATTATATATTAT | 221178 |
rs28868661 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190225 | ACATATCATATATAA[A/T]ATATATTATTATATA | 221178 |
rs33928363 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159132 | TTTAGACCGTGATAT[-/G]TTTTTTTTAAATAAT | 221178 |
rs33950980 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084551 | TTTTTCTTAAAAAAA[-/A]GCAACACTACACAGT | 221178 |
rs33990382 | snp | C/T | 0.463786 | 0.129597 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24302614 | CTACAACAGGTGCCC[C/T]GTGGCCCCACCGCAC | 221178 |
rs34009093 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210084 | AAAAAATGTTCAGTT[-/C]CCTTTGTACATTTTG | 221178 |
rs34013613 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24236820 | GGTACGGCTGCTGTG[-/A]AAAACAGTGTGCTGA | 221178 |
rs34017703 | in-del | -/A | 0.388021 | 0.208447 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294615 | AGGGAAACAGTGGCT[-/A]ATGACGTAAATGTCA | 221178 |
rs34022997 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283035 | TGTGTGCCCCCGATC[-/T]TTTGCAGTCTTGTCT | 221178 |
rs34036185 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24088188 | GTGTCCTGGCAGACA[-/G]GGGAACTGGCGTGTT | 221178 |
rs34039001 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159919 | ATTAGCTGCCTATCA[-/G]GGGAACATGGAGCAC | 221178 |
rs34048525 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24218642 | GCCGCAGGCTGCATG[-/T]GGCCCAGGGAAGCTT | 221178 |
rs34056281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241365 | TCCCAAGATGGTCCC[C/T]AAAGTAGCAGAAACT | 221178 |
rs34057898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099085 | GTGAGATCCTGTCTC[C/T]AAGAAATTTAAAAAT | 221178 |
rs34060296 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283546 | CAGGGTGGCCAATCT[-/A]AAAAGCTGCACCATC | 221178 |
rs34079432 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109181 | TCTCATTGTTCAGTT[-/C]CCCACCTATGAGTGA | 221178 |
rs34081186 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986396 | TTATCGAGCCAAATT[-/C]CCCAGAGATTTACAT | 221178 |
rs34082142 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079597 | TAGTAATACAGGGGG[A/G]TCCTGACGGCTTGAG | 221178 |
rs34098656 | in-del | -/T | 0.46875 | 0.121031 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146643 | GGAAATGCACAGCAA[-/T]TTAAAAAAAATGCCA | 221178 |
rs34102283 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248324 | TGCTGTTTCCCAGGG[-/A]AATGGCTGCAGAGCC | 221178 |
rs34108214 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24251314 | ATGGCCACCCTGGCC[-/G]GGGTTTGTGGCCTTG | 221178 |
rs34123045 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108885 | AACACATTTGTATTT[-/G]GCTTTGTCTTCCAGA | 221178 |
rs34130502 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151006 | AAAGAGTTGACAAGT[-/C]CCCTGTCTGGGGTCT | 221178 |
rs34133498 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228897 | ATATCATACTGTCCT[-/A]AAAATAACAAAATAA | 221178 |
rs34145507 | in-del | -/A | 0.474903 | 0.109173 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135698 | GCAAGAATCCGTCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs34173919 | snp | C/T | 0.432797 | 0.170544 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074895 | AGTAAGGCACAGACA[C/T]AGCTAGGCTGGGTGC | 221178 |
rs34175373 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986425 | TGTGTTATCTGCAGG[-/A]AAGAGGGTTTTGATT | 221178 |
rs34182915 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019298 | TTCACCGTTTTAGCC[-/G]GGGATGGTCTCGATC | 221178 |
rs34196300 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271840 | AGTCTGTGCTTTCTT[-/C]CCTTGTTTTGATTGG | 221178 |
rs34209004 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038910 | GGCTAAAAGGGAGCA[C/T]ACAAATCCAGAGAAA | 221178 |
rs34211405 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159404 | ATTATCATTAATCTT[-/G]GGAGTGTGCTTTAAT | 221178 |
rs34212273 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23988547 | TTGCTGAGAAGAACG[-/T]TTTTGGGCACATTAA | 221178 |
rs34221097 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292996 | TGAGACTTTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 221178 |
rs34235959 | in-del | -/TA | 0.459574 | 0.136304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038361 | TAGTTCCCTCTGTTC[-/TA]TGTTTACATTGGAGT | 221178 |
rs34238632 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085167 | TTGCTCTGTCACCTA[-/G]GCTGGAGTGCAGCGG | 221178 |
rs34240045 | in-del | -/T | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090117 | ACTGGACTTCCTTTA[-/T]TTTTTTTTTCTTCTA | 221178 |
rs34242537 | in-del | -/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173511 | CCCCCGTCCCCCAAC[-/T]TTTTTTTTTTTTTTG | 221178 |
rs34260069 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217055 | GACTCTGTCTCAAAA[-/C]CAAAACAAACAAACA | 221178 |
rs34278390 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109730 | CTTTTTTGCCCCCCA[-/G]GATTACATGGATAGA | 221178 |
rs34295974 | in-del | -/TACT | 0.349013 | 0.229557 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037400 | CAGGTTCTCGACTAA[-/TACT]TTATTTATTTATTTA | 221178 |
rs34308776 | snp | G/T | 0.450859 | 0.148847 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186106 | CAGCAACATCCAGAC[G/T]GGTGTTTGGCCAAAT | 221178 |
rs34312565 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092822 | GTGGAGCTTTTATAC[-/T]TCCATAGACTCCACT | 221178 |
rs34354611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285212 | TTCCTGACTTTTTAA[A/T]TGTTAACGATCTCAA | 221178 |
rs34359264 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23990440 | CCAATAGTGATTTCT[-/A]CAATTCCTTAAACTC | 221178 |
rs34363429 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109235 | TTCTTGTGATAGTTT[-/C]CCTGAGAATGATGGT | 221178 |
rs34370788 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24005469 | TTAAGTACGAGAAAT[-/G]GGAGTGTATGCAGGG | 221178 |
rs34371369 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993971 | GTGATGGTGGTGGTG[-/T]TTTTTTTTTTTTTTC | 221178 |
rs34382903 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996901 | TTCCCTTATAAGGAT[-/C]CCTTGTGCTCACAGT | 221178 |
rs34406412 | in-del | -/AGTAG/GAGTA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086067 | TCACTGTGGGAGTAG[-/AGTAG/GAGTA]CAGGAGAAAGCTGGA | 221178 |
rs34412501 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024452 | CCCTCATTCTCTTGG[-/TT]GTTGTCTAGTGACAA | 221178 |
rs34449055 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24301266 | TATTTTCCTGACTGC[-/A]AAATGCAAAAACAAG | 221178 |
rs34471815 | in-del | -/ATC | 0.494526 | 0.0520291 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045122 | CTATGTATAATTTAT[-/ATC]ACTCATTGCCAATCC | 221178 |
rs34472292 | in-del | -/T/TT | 0.437259 | 0.165632 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102476 | CTTCACAGAATTTCT[-/T/TT]TTTTTTTTTTTTTTT | 221178 |
rs34474431 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092915 | ACATTAAGTTGAATG[-/T]TTTTGGTGTTTGGCA | 221178 |
rs34478194 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150234 | CCACTTCTCCAAACA[-/C]CCTGGGTTTCTCCCT | 221178 |
rs34497355 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996744 | ATGTGAGGAGGCAGC[-/T]TTTAGGCCACACATA | 221178 |
rs34505499 | in-del | -/AGG | 0.0525931 | 0.153397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232256 | TCAGTGTTCCTGGGC[-/AGG]AGAAGGTGGATGTCT | 221178 |
rs34509019 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156419 | GATGGCACACTGGAT[A/C]TGGCTCCTGGCCCAC | 221178 |
rs34511656 | in-del | -/AT | 0.215747 | 0.247642 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206288 | CACTAAAGAAGACAC[-/AT]GTGGCCACAAAACAT | 221178 |
rs34511956 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143560 | TGTGTTTTCTAACTT[-/A]AAAAGTTGCTCCTTT | 221178 |
rs34553109 | in-del | -/T | 0.498034 | 0.0312882 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043674 | GTAACTTTGAGGGAA[-/T]TTTTTTTTGTTGTTG | 221178 |
rs34555225 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291410 | CTTCTCTATTTAGAA[-/G]GGGGTGAGGGCACAC | 221178 |
rs34568213 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246353 | GAGAAAATAATATTA[A/C]CCTTTTCATGATTTC | 221178 |
rs34572345 | in-del | -/C | | | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270815 | GGCTCCTCGGTCACA[-/C]CCCCAGTCCTGCTCT | 221178 |
rs34577072 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201165 | TGCTTATTAGCACAA[-/G]GGGGCGGGTTTCCAA | 221178 |
rs34615845 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003061 | TTCCCTGTGGCCATT[-/G]GACTCAGTCTTCCGA | 221178 |
rs34619988 | in-del | -/CTCT | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292055 | GCCACCGCGCCCGGC[-/CTCT]CTCTGTCTTTATTAT | 221178 |
rs34624030 | in-del | -/C | 0.403334 | 0.197456 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999610 | TCAGGGTGGATTCTT[-/C]CTGCCTGAGCTGCAG | 221178 |
rs34624842 | in-del | -/TATG | 0.491316 | 0.0653198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067336 | ATGCTTCCTGAGCTA[-/TATG]TATGTACCCTTTGTA | 221178 |
rs34631817 | snp | C/T | 0.263535 | 0.249633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276917 | GAGCTGGCATTGACA[C/T]GCTGTGGACTACTAC | 221178 |
rs34655514 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275833 | CAGCTACTCGGTAGT[C/G]TTAGGCAGGAGAATC | 221178 |
rs34668799 | in-del | -/AAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999387 | AAAAAAAAAAAAAAA[-/AAA]GCCTGTTCGGATATT | 221178 |
rs34673192 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235041 | CCACAGTGCCTTGGA[A/C]CATGGTAAATCGGGT | 221178 |
rs34688488 | in-del | -/T/TT | 0.658496 | 0.0527193 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185724 | TACAAATAGATGCAG[-/T/TT]TTTTTTTTTTTTCAT | 221178 |
rs34690904 | in-del | -/AC | 0.126513 | 0.217373 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043480 | ACCTTGATTGATATT[-/AC]ACACACACACACACC | 221178 |
rs34695723 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24123101 | TCACTATATTCACAG[-/C]ATCATTTTCTGAATT | 221178 |
rs34706946 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24266332 | TCTGTCACCCAGGCT[-/G]GGAGGGCACTGGCCC | 221178 |
rs34735514 | in-del | -/GGC | 0.34101 | 0.232846 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108663 | CTTTTCATGGTAGGG[-/GGC]GGGGGGAAGCCTGAT | 221178 |
rs34740517 | in-del | -/T | 0.467946 | 0.122472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010474 | AGGGAGGTATGTAGC[-/T]TTTTTTTTTTTTTTT | 221178 |
rs34742184 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24244365 | TAGGCCTCTGAATGG[-/C]ATATAAGAGAAATCA | 221178 |
rs34749958 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24141565 | ATATTCCTCTGTTAT[-/A]AGAGCTTATCCAGAT | 221178 |
rs34761477 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24231107 | CCTGTTCCCACCCAA[-/G]GACTAGGCCACAGCT | 221178 |
rs34769600 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189485 | TCTCTCTCTCTCTCT[A/C]TATATATACGTGTAT | 221178 |
rs34775216 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144081 | AATGTTCATGAGCTG[-/A]AATGTGCACTAACTC | 221178 |
rs34789567 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182773 | TGTCATTTCTAGTAA[-/T]TTTTGTTCTGCTGGG | 221178 |
rs34795511 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239094 | TAATAAAAGTATAGA[A/G]GCTTATTGTTGGCAA | 221178 |
rs34798211 | multinucleotide-polymorphism | AA/TC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246537 | GCGTTTGTGCGTGTC[AA/TC]TGTGTGTGAGAGACA | 221178 |
rs34798653 | snp | A/G | 0.105214 | 0.203807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044893 | TCCAGAGGAGGGGGT[A/G]GGGGTGGGGGTAGGC | 221178 |
rs34810612 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204337 | GAATCTTCCTGAATC[-/A]AAATATATTTTGGAA | 221178 |
rs34827671 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272103 | GGGTGCTCCCTCCCA[-/G]GGTTCCTGCACCCAT | 221178 |
rs34832306 | snp | C/G | 0.494651 | 0.0514399 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126541 | TATATATATTTGTGT[C/G]TGTGTGAGAGAGAGA | 221178 |
rs34838879 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180556 | TTTTGATAGGATTGT[A/G]CTGAATCTGTAGCTG | 221178 |
rs34845839 | in-del | -/C | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254126 | AGCCATCCCCATTTT[-/C]CCGTGGGTGCTCATT | 221178 |
rs34859599 | multinucleotide-polymorphism | AG/CC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086827 | CTGGGTAGTGGCAGC[AG/CC]CTGAAGCCAGCAATG | 221178 |
rs34865314 | in-del | -/G | | | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307428 | TGCCACAGGAGCTGT[-/G]GCTAGTGGCCCTGCT | 221178 |
rs34868919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046205 | AGGTTAAGAAACAGC[C/T]TCAGAAACCCTCCTC | 221178 |
rs34875690 | snp | A/G | 0.198944 | 0.244731 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989776 | TGGTATCAGAAGTGA[A/G]GCCTTGGGAAGTGAT | 221178 |
rs34893019 | in-del | -/C | 0.362941 | 0.223034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116738 | TAGACTTAACTGTGT[-/C]CCCCAAAATTTGTAT | 221178 |
rs34901396 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098594 | GAGTGAGACTGTCTT[-/A]AAAAAAAAAAAAAAG | 221178 |
rs34911153 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24007146 | TCTGTCAGTGCCTCT[-/C]CTGATTGCCAAGCAT | 221178 |
rs34916680 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989346 | GAATTGCTTCAACCT[-/G]GGGAGGTAGAGGTTG | 221178 |
rs34917706 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024450 | ACCCCTCATTCTCTT[-/G]GGGTTGTCTAGTGAC | 221178 |
rs34919241 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113548 | GAAAGCTACTTCTGT[-/A]AAAACAAGCATATTA | 221178 |
rs34922445 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24069109 | TGGCTGTTTGGGCTC[-/T]TTTTTGATTTCATAT | 221178 |
rs34924085 | in-del | -/A | 0.311808 | 0.242239 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135219 | ATTCGAAAAAAAAAA[-/A]TACTTTTTCTTCTCT | 221178 |
rs34929754 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037896 | TTCCCCCCAGTAAAA[-/G]GGTTAGTAACAACTA | 221178 |
rs34932858 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108661 | TGCTTTTCATGGTAG[-/A]GGGGGGGGAAGCCTG | 221178 |
rs34948971 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24257555 | AAGTTGACTTGCTTT[-/A]AAAAATGTTTCTAAC | 221178 |
rs34983901 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103484 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs34989212 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987694 | GGCATTCAGCACATT[-/C]CACATTACTGTGCAA | 221178 |
rs35001100 | in-del | -/C | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161802 | TATTCAGCTCTTGTT[-/C]CCCATGGCTTCCCAT | 221178 |
rs35028588 | in-del | -/A | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042444 | AGTGCTTCTGTTTCC[-/A]AAGCAAACCAGGCTG | 221178 |
rs35053977 | in-del | -/AAAA/AT/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293022 | AAAAAAAAAAAAAAA[-/AAAA/AT/T]GGCGAGGGTGTGGGG | 221178 |
rs35060329 | in-del | -/A | 0.482534 | 0.0918038 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258384 | TGAAGAGTTCATCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs35065399 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24069485 | GCATCCTGAGACATT[-/G]GTTGAAGTTGTTTAT | 221178 |
rs35072898 | in-del | -/C | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253355 | AACCCTCTCTCTCTT[-/C]CCTAGAAGGAGACAC | 221178 |
rs35084534 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000320 | CTGATACAAAGATAG[-/T]AAAAGGTTTCAAAGG | 221178 |
rs35084740 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147722 | CCAGAGCTGAAACTG[-/A]AAACCCTGTACCCAT | 221178 |
rs35088272 | snp | A/T | 0.220843 | 0.248294 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192187 | GGCACAAAAGCAGCG[A/T]TGTAAACTCTTGTTG | 221178 |
rs35152336 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083222 | AGTGGAGACCCCCTA[-/G]GGCAATAGAATAGAA | 221178 |
rs35152567 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227952 | CACTCTGTCACCAGG[A/C]TGGAGTGCAATGGTG | 221178 |
rs35154160 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295181 | GCAGCCACATAACAT[A/G]GTAGTAGAAGTATGG | 221178 |
rs35155551 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210523 | AAGAGACTATCCTTT[-/C]CCCCATTCTTGGTGC | 221178 |
rs35175380 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277922 | GAAATCCCACTCCAT[-/A]AAAACACACTTGAAT | 221178 |
rs35197911 | snp | A/G | 0.426201 | 0.177351 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221721 | ATGTGTGGGATGGGC[A/G]TGGGTGCAGTAGTGT | 221178 |
rs35210715 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217057 | ACTCTGTCTCAAAAC[A/C]AAACAAACAAACAAA | 221178 |
rs35212902 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24004367 | ACAGTTAGTGTGGCA[-/C]ACTGTGCTTACTTAT | 221178 |
rs35213882 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240918 | TTTAAAATGTTTAAC[-/A]AAATGACCAAACTGC | 221178 |
rs35228471 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24153398 | TCCATTTCATTGCCT[-/A]AAAAGGAACTTGTTC | 221178 |
rs35259542 | in-del | -/A | 0.0425829 | 0.139564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247926 | CCATTTTGGTTTCTC[-/A]AGGAGGGAGCCGGTG | 221178 |
rs35270570 | snp | C/T | 0.426813 | 0.17674 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996416 | CAATTGGGCAAAAAA[C/T]GATCTGCAAATCAGT | 221178 |
rs35272951 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291735 | TACACTCTCTCTCTG[G/T]CTTTATTTTTTTTTA | 221178 |
rs35282665 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221826 | ATTCTTACCTCTGAA[-/T]TTTTTTTTTTTTTTT | 221178 |
rs35307162 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042499 | CTCACGAGTCACTGA[-/G]GATCAGAGACACAAG | 221178 |
rs35347296 | in-del | -/G | 0.497566 | 0.0347987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135225 | ATTATTCGAAAAAAA[-/G]AAATACTTTTTCTTC | 221178 |
rs35350652 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221561 | ACAGATGTGCATGAT[-/G]GGGGAAAGCATGGAC | 221178 |
rs35355340 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154127 | GATACAAGCATTTTG[-/A]AAAAAAAAAGCTTGG | 221178 |
rs35360707 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24289470 | AGGGTTATGCCATAA[-/G]GAACTATGGAGTCCT | 221178 |
rs35363577 | in-del | -/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978881 | AAAATTTTTTTTTTT[-/T]GGTAGAGATGGCGGT | 221178 |
rs35368874 | in-del | -/C | 0.329928 | 0.241884 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159110 | GAGATAATAAAAAAA[-/C]CCCTCAATTTAGACC | 221178 |
rs35400287 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142111 | ATTTGTAGGGAAAGG[-/T]TTTTTTTTTTTAGCT | 221178 |
rs35422041 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24031277 | TTTAGCACAGACCAA[-/G]GGTCTGGTCCGTAGC | 221178 |
rs35427133 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246696 | AACCGTGTCTCTGCT[-/A]AAAAATGTATATCTA | 221178 |
rs35477867 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24145120 | CCTTCTTTTCAACTT[-/C]CCTGGCAATACTGAC | 221178 |
rs35494448 | in-del | -/AA | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219003 | ATTCTCATTATCACC[-/AA]AAAAAAAAAAAAAAA | 221178 |
rs35503472 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221806 | ATTCTTACCTCTGAA[-/T]TTTTTTTTTTTTTTT | 221178 |
rs35511750 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107237 | TTTTGAACAAGAGGC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs35521221 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046347 | CACCAGGCTGGAGTG[CA/TG]GTGGTGTGATTATAG | 221178 |
rs35526368 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24166012 | ACTTCCACCCTTCCT[-/G]GGGGGGTGGAGTGCT | 221178 |
rs35526844 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077726 | ATGCTGTAGGCCCCA[C/G]GACCGTGTATAATCC | 221178 |
rs35527820 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184499 | CAACCAAATCACAAA[-/G]GATTATCACTTTTTT | 221178 |
rs35553897 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207562 | GTACACCCGGGTTCG[-/CA]TTTCTCCACATCCCT | 221178 |
rs35583340 | snp | A/C | 0.170733 | 0.237101 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233076 | TTAATATATGAACAT[A/C]TGTTTATCCAGCCTC | 221178 |
rs35588253 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242981 | ATAGTGAGATGCTAC[-/T]TTTTTGACTTCTTAA | 221178 |
rs35599239 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227592 | TTTTTTTTTTATTGA[-/G]GACAGTCTCATTCAG | 221178 |
rs35620921 | in-del | -/AG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135720 | AAAAAAAAAAAAAAG[-/AG]TATTTTTAGATAGAG | 221178 |
rs35654406 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996410 | CAATTGGGCAAAAAA[-/A]CGATCTGCAAATCAG | 221178 |
rs35663311 | in-del | -/C | 0.464841 | 0.127841 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023396 | TAACTGATTTGGATA[-/C]TTTGCTTTTTATCTT | 221178 |
rs35663381 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24149598 | AGGCCACCTAACACT[-/C]CCTAGATCTTCTGTC | 221178 |
rs35668729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251972 | TCCCTTGGGCCAGGG[C/T]GCGTTTGTCTGGGAG | 221178 |
rs35669430 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040987 | ATGAGGCCAGGTGCT[-/G]GGTGGGTCACATGGT | 221178 |
rs35670220 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24050252 | TGTTAAGTATAATAG[-/A]ATATTAAAAAATAGA | 221178 |
rs35673940 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24218723 | TTTTTTTTTTTGCGA[-/T]TTTTTTTTTTAATCT | 221178 |
rs35681030 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173646 | TATTCCTGTCTCTCT[-/A]AAAAGGTTTTAAACT | 221178 |
rs35689312 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204250 | GAGTCTCTGTTATTG[G/T]TATCCACATTTTTCA | 221178 |
rs35716533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111432 | CCCACCCCAGAAACA[A/G]AGTCTTGCTCTGTCA | 221178 |
rs35718016 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24094993 | CACTATGTAAAACAT[-/G]GGAGATTTCTCAGAA | 221178 |
rs35757898 | in-del | -/A | 0.495095 | 0.0492773 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081711 | TAAATTTAAAAAAAA[-/A]TTAAAAATTGCACAC | 221178 |
rs35768526 | snp | C/G | 0.021709 | 0.101898 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270856 | GTTTTCCAAACAGAA[C/G]GATGGTAGCTAGAGG | 221178 |
rs35769572 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164613 | GAGCAAGTTAAGTTT[-/C]CATTGCTCCCTAAAT | 221178 |
rs35776484 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271021 | CTCCACTCTCTCTCA[-/CT]CTCTCTCTCTCTCTC | 221178 |
rs35792923 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124876 | TTGTCAGATTTTTTG[G/T]CTTATTTTTTTTCTA | 221178 |
rs35793500 | snp | C/T | 0.0587935 | 0.161059 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24294781 | TGAGGCCATGAAGAA[C/T]GTGGCCTGTCTGATC | 221178 |
rs35793567 | in-del | -/A | 0.418974 | 0.184249 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074639 | AGGAGTAAAGTGATT[-/A]AAAAAAAAACCCTTG | 221178 |
rs35802534 | snp | A/G | 0.370162 | 0.219229 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996749 | GAGGAGGCAGCTTTA[A/G]GCCACACATAATTTA | 221178 |
rs35816429 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160130 | CGTTTTCCTTTCACA[-/G]GGGAGTGAACTTCTG | 221178 |
rs35818263 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24087257 | AGGGGCCTGGGACCT[-/C]CCCAGTCTTGCCTGA | 221178 |
rs35845040 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24194154 | AGACATTGAGACACC[-/T]TTGTAGAACCTAGGC | 221178 |
rs35854155 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110226 | TCTGCTCGCTGAGCC[-/G]GGCTCTCCCAGAACC | 221178 |
rs35866742 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193236 | GTGACGGAGCTCTGA[-/G]GAAGGGGAGTTGCAG | 221178 |
rs35877828 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193905 | AGAAGATCAGTAATT[-/G]GGGATTTTAACACAT | 221178 |
rs35887179 | in-del | -/CATACT/TCATAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23995231 | ATTATTTATCATACT[-/CATACT/TCATAC]TAGCTGATCTTCTGA | 221178 |
rs35892461 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070273 | GGCAACAGAAATGTC[C/T]GAGGAAATTAGCCCT | 221178 |
rs35912994 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249569 | AGATGGGGCTCTGGG[-/C]AGACGGCCAAGGCCT | 221178 |
rs35932847 | in-del | -/T | 0.299664 | 0.245017 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996655 | GATTAAAAGAGTAGC[-/T]TACAGGAGGATGTTT | 221178 |
rs35934615 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24168466 | GGCCCCAGTACACTT[-/C]CAGTGTTTGTTGCAA | 221178 |
rs35934663 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285164 | GCAAAATCACCTGCT[-/A]CCCGTGGCCAGGGGA | 221178 |
rs35973334 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013465 | CCTGGGACACTGCTT[-/G]GGGGACAGTGCCCAG | 221178 |
rs35984887 | in-del | -/T | 0.409041 | 0.192888 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100744 | GGAGACACTAGCAGA[-/T]TTTGCTCTTACCTGA | 221178 |
rs36000954 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204168 | CCAGAGGCTAACCCG[-/A]AATGCCTGTTATGTG | 221178 |
rs36019629 | snp | A/G | 0.00262611 | 0.0361408 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24286381 | AGCCTGGTTCCCCGC[A/G]AGCTTCGTCAGAGTA | 221178 |
rs36023890 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23982191 | CAGATTTCTTACTTT[-/C]CCACTTGCAGCCACA | 221178 |
rs36028125 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987556 | AGCATTTTTTTCTCC[-/A]AAAGACCTGATTTTG | 221178 |
rs36049451 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133915 | AATCAGACAGCGCAT[-/C]CCAGAGTGGGGGTTT | 221178 |
rs36073606 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048577 | TTTTTTTCTCCTTTG[G/T]ACTTTATAAAATTTC | 221178 |
rs36103508 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172814 | TTAGCTAGCTCCCTT[-/G]CCCTTTCTGTATTAA | 221178 |
rs36111662 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143676 | CTGATACCACCCACA[-/G]GGGAACCCGAAACGT | 221178 |
rs36119769 | snp | C/T | 0.488057 | 0.0763479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102675 | GATGGGGTTTCACCA[C/T]GTGGGCCAGGCTGGT | 221178 |
rs36152248 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190369 | ATATTATTATATATA[-/C]ATATATGATATTATA | 221178 |
rs36182818 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190368 | ATATATTATTATATA[-/T]ACATATATGATATTA | 221178 |
rs41286100 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017533 | TGTAAGATATACACA[C/T]ATATGTATATATACA | 221178 |
rs41287016 | snp | A/G | 0.106611 | 0.204791 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249561 | CCCAAGAGGAGATGG[A/G]GCTCTGGGAGACGGC | 221178 |
rs41287018 | snp | C/T | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270666 | TAACCCTTGGTCACA[C/T]GGAGTGTGGAGCCAG | 221178 |
rs41287020 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273282 | GGGTCTGGAGCCAAT[G/T]GGGTGTTGGCTGCCC | 221178 |
rs41287032 | snp | A/G | 0.138926 | 0.22397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290891 | GGAACACGGGTGAGG[A/G]GCATGGGTAAGGGGC | 221178 |
rs41314440 | snp | C/T | 0.0329542 | 0.124061 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224368 | AGAGCCCCCAGAGCC[C/T]CGGGGCAGGAAGTGC | 221178 |
rs41502045 | snp | C/T | 0.182614 | 0.240747 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279939 | AACATCATGGATTAG[C/T]AGTTAGCGACACTGC | 221178 |
rs45486904 | snp | C/T | 0.095934 | 0.196885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278476 | TAGAGATGGGTCTTA[C/T]TATGTTGCCCAGCTT | 221178 |
rs55668663 | snp | A/G | 0.3746 | 0.216737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007974 | CAGAAGTCCTGGGGG[A/G]AAATGGAGGCAGGCG | 221178 |
rs55689127 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072843 | TTTTTTTTTTTTTTT[-/T]ACATCCCCTTAAGTG | 221178 |
rs55720802 | snp | C/T | 0.243633 | 0.249919 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178005 | GGGACTATGGGTGTG[C/T]GCCACTATGCCTGGC | 221178 |
rs55722906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035127 | AAATTAACATCCTAT[A/G]CTTATTGGGCATTGT | 221178 |
rs55744764 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278958 | TCCTTCCCTCCTTCC[C/T]TCCTTCCCTCCTTCC | 221178 |
rs55745550 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036022 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAAAAGAAA | 221178 |
rs55782562 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245494 | GTTTTGCTATTTTTA[A/G]AATATGTGGTACCTT | 221178 |
rs55800191 | snp | A/C | 0.422315 | 0.181128 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101499 | TGGTGAAAAAAAACA[A/C]CACATAAAACTTACC | 221178 |
rs55814109 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180176 | CTATTTTGCATATGG[A/T]GTAAGGGAAGATCTC | 221178 |
rs55815519 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278966 | TCCTTCCTTCCTTCC[C/T]TCCTTCCCTCCCTCC | 221178 |
rs55831614 | in-del | -/CACACACACACACACACACACACA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201044 | AGTCACACACACACA[-/CACACACACACACACACACACACA]GAGTTTGGATTTTGA | 221178 |
rs55848100 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212313 | AAAAAAAAAAAAAAA[-/A]GGTCGAGGGAAACAA | 221178 |
rs55860369 | snp | A/G | 0.175897 | 0.238765 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279726 | AAAACTGAAGCTCAA[A/G]GAGCTGAAGTGACTT | 221178 |
rs55865084 | in-del | -/CTTTTCTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118915 | CTTTTCTTTTCTTTT[-/CTTTTCTTT]TTTTTTTTGAGATGG | 221178 |
rs55881452 | in-del | -/A/AA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239719 | AAAAAAAAAAAAAAA[-/A/AA]TAGAGAAAGCAGGTT | 221178 |
rs55881897 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194569 | TCCGTAACAGTTTGA[A/G]GATTTGGTAGTCAGT | 221178 |
rs55884031 | snp | A/G | 0.263323 | 0.251196 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170854 | AACAACAGCAACTCC[A/G]AAAAGTATAGGTTTA | 221178 |
rs55898650 | snp | A/G | 0.117188 | 0.211804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079056 | AACCAGAAAATTGGA[A/G]AGGGCTTCTTGGAGG | 221178 |
rs55913786 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278988 | CCTCCCTCCCTCCCT[C/T]CCTCCCTTCCTTCCT | 221178 |
rs55947442 | snp | A/G | 0.307176 | 0.243374 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034764 | GATTTTCACAGCACA[A/G]CAGCAGGGGCTGAGA | 221178 |
rs55953024 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994055 | ATGAAGTGATTGCCA[C/T]GCATTGGCGTCACAG | 221178 |
rs55953887 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182650 | ACCTCCCCCAGGCCC[C/T]GCTTCAACACTGGGG | 221178 |
rs55973344 | in-del | -/TTCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278922 | TCCTTCCTTCCTTCC[-/TTCC]CTCTTTCCTTCCTTC | 221178 |
rs55988908 | snp | G/T | 0.496034 | 0.0443518 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042447 | GCTTCTGTTTCCAAA[G/T]CAAACCAGGCTGCTG | 221178 |
rs56026405 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251186 | TGCCGTGTGAGTTTG[A/G]GTAAGCAAGGCTTGC | 221178 |
rs56078056 | snp | A/G/T | 0.00179207 | 0.0298831 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286168 | CTCCCTCACCATCCC[A/G/T]CCCACTCGTGCTCTA | 221178 |
rs56085171 | in-del | -/AAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277467 | AAAAAAAAAAAGAAG[-/AAG]TTCACCTTGGAAGTA | 221178 |
rs56087317 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127859 | ATCAAGTCTGGTACA[G/T]CTTCATTTATTTCTT | 221178 |
rs56089905 | snp | C/T | 0.49614 | 0.0437598 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042124 | TTTGCTGAGAAAGCG[C/T]GGTGTCCTCTGTGTC | 221178 |
rs56169990 | snp | A/C | 0.108048 | 0.20579 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056770 | GAATGAAGAAAAGAC[A/C]AGTACGTTGCTGTGC | 221178 |
rs56178489 | in-del | -/CCTCTGT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042136 | CGCGGTGTCCTCTGT[-/CCTCTGT]GTCACGGGAGCGTTG | 221178 |
rs56198152 | snp | A/G | 0.0498117 | 0.149749 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303713 | GAGTTCGAGACAAGC[A/G]TGGCCAATATGGCAA | 221178 |
rs56224822 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136907 | GGATCTCGGCTCACT[A/G]CAAGCTCCGCCTCCC | 221178 |
rs56249473 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015749 | GGCAGGCCCCCCCCC[-/A]ATTCCTAGGTCCACC | 221178 |
rs56258822 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278950 | TCCTTCCTTCCTTCC[C/T]TCCTTCCTTCCTTCC | 221178 |
rs56331495 | snp | C/T | 0.308908 | 0.242961 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036174 | CAATAAAAATTCCAT[C/T]ACATAAATTCCATAT | 221178 |
rs56397321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274200 | TGTGGCTTGCTGCAT[C/G]GACAGGCAACAAAAG | 221178 |
rs56401386 | in-del | -/ACAC | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233925 | CACACACACACACAC[-/ACAC]TGATAAGATTATTTC | 221178 |
rs56663126 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24033883 | TAGAGCTTATTTGGC[C/T]TTTATCATGTATCAA | 221178 |
rs56667767 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186714 | TTCTGCACAGAAAAT[A/G]CAGGTTTGAGAGGGA | 221178 |
rs56678093 | snp | A/G | 0.340784 | 0.232934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028930 | TTTAAACATGAAAAT[A/G]TTTTATAATCTACAT | 221178 |
rs56702717 | snp | A/C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173510 | CCCCCCCGTCCCCCA[A/C/G]CTTTTTTTTTTTTTT | 221178 |
rs56704036 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296458 | TTTTTCTTTTTGATT[G/T]TGGACGCTGACATTT | 221178 |
rs56704592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183455 | CTTTCTATGTTGTAA[C/G]TTTTCCAAGAGGTAC | 221178 |
rs56716982 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139768 | TACCTGTTTTTGTTT[C/T]AAAATCTGTAACATG | 221178 |
rs56724430 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010240 | CTTAGTCTGGCTCAG[C/T]GAATCTGCATTTTTA | 221178 |
rs56837096 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036032 | AAAAAAAAAAAAAAA[-/AA]GAAAGAAAGAAAAAA | 221178 |
rs56884585 | in-del | -/T | 0.437542 | 0.165312 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175231 | TTTTTTGTTTTTTTT[-/T]AATTTGTTTTTGTTG | 221178 |
rs56933040 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206592 | AATATAAATCATTCT[A/G]TTATAAAGATACATG | 221178 |
rs56948264 | in-del | -/AGTA | 0.067446 | 0.170804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197278 | ACACAACAGAGACTC[-/AGTA]GGAAGAAATTGTAAA | 221178 |
rs56953359 | in-del | -/TGGTGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044900 | AGGGGGTGGGGGTGG[-/TGGTGG]GGGTAGGCAGAGTGA | 221178 |
rs56959847 | snp | A/C | 0.275197 | 0.248727 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275966 | AATGTTTTTTCCACA[A/C]CAATTTTTTCAACAA | 221178 |
rs56971121 | snp | A/G | 0.411242 | 0.191052 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030064 | CACACACACACACAC[A/G]CGCACACACACACAC | 221178 |
rs56997064 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197431 | TTATTTAGCTCATCA[A/G]TGAGGGAACCAGCAG | 221178 |
rs57012558 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151972 | AGCTGTGAAGATGTG[A/G]TTCAGTTCTCAGGGA | 221178 |
rs57036711 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173065 | TTTTTTGAGTCATTA[C/G]AAAGTGGTATTATGT | 221178 |
rs57060476 | in-del | -/A | 0.212425 | 0.24716 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181850 | CGGGTGTGGTGGCTT[-/A]ACACCTATAATCCCA | 221178 |
rs57082291 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242070 | AAAAAATGAAAAAAG[A/G]AAAGAAAGATTATTC | 221178 |
rs57082953 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287381 | TTGCCGAGGCTGGTC[A/G]CGAACTCATGGACTG | 221178 |
rs57132705 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173090 | TTATGTAAATATATA[C/G]TTTTTGAGACACAGT | 221178 |
rs57135846 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981491 | ATTAGAAAAATTCAC[A/C]GTTTCGGGAGCCGGA | 221178 |
rs57143109 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201066 | ACACACACACACACA[-/CA]GAGTTTGGATTTTGA | 221178 |
rs57153567 | snp | A/G | 0.28052 | 0.24813 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291526 | GCTGGGCCCTGAGCC[A/G]TTCCCTACCCACCGG | 221178 |
rs57166187 | snp | A/G | 0.106987 | 0.205054 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177297 | GGCATATGTCAGTGT[A/G]TCTGGCTGTGCCTGG | 221178 |
rs57175692 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242832 | CATCTGGGATCCTAT[A/G]CGTTCCCCTCACCCA | 221178 |
rs57266761 | snp | C/T | 0.148326 | 0.228391 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012307 | TTAGCCTCTGAGGCA[C/T]AGGGCAGCTCACAGA | 221178 |
rs57269031 | in-del | -/ACACAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24233887 | ACTTTATACACTTAA[-/ACACAC]ACACACACACACACA | 221178 |
rs57284151 | in-del | -/GTGT/GTGTGT/GTGTGTGTGT/GTGTGTGTGTGT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987040 | TGTGTGTGTGTGTGT[lengthTooLong]TACTACTCCACATGG | 221178 |
rs57319211 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197414 | GAATATGTGTCAGAA[A/T]TTTATTTAGCTCATC | 221178 |
rs57338107 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156221 | GATTGCTGGATGATA[C/T]GGTAATTCTAGTTTT | 221178 |
rs57346440 | in-del | -/A | 0.308166 | 0.243139 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993145 | TGAACCTGCTGTGGC[-/A]GAAGGTCGTGGACAG | 221178 |
rs57348211 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188396 | ATTAAGAAAGTGAAA[-/CA]GCCTTATCGCTGATA | 221178 |
rs57348867 | in-del | -/T/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280506 | TTTTTTTTTTTTTTT[-/T/TT]GGCTCAACCACGGTT | 221178 |
rs57356256 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037946 | AAATGGAGTCTCGCT[A/C]TGTCACCCAGGCTGC | 221178 |
rs57425747 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284429 | ACTTTGGAAGGCCAA[A/G]GCAGGTGGATCATTA | 221178 |
rs57437676 | in-del | -/TTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191524 | TTTTTTTTTTTTTTT[-/TTTT]GAGATGGAGTCTTGC | 221178 |
rs57459477 | snp | C/T | 0.34146 | 0.23267 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114607 | TTGATTTTTTATTTT[C/T]GAAGGAGCTCAAGGT | 221178 |
rs57488344 | in-del | -/TTCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052070 | GACGCAGGGTTTGGC[-/TTCTT]ACACCAGCATCCTGT | 221178 |
rs57524052 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296504 | AGAAGTTAATTTCTT[C/G]CTGACAATTTATCGT | 221178 |
rs57532147 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276976 | TTGCTATTTCCCCAT[C/T]AGCAATTCGTAATTC | 221178 |
rs57570010 | in-del | -/A | 0.177201 | 0.239166 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077627 | TCTAAAATAAAATTT[-/A]AAAAAAAAAGACAAA | 221178 |
rs57682310 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196911 | GGCTAGAAAAAAAAA[-/A]CAGTTTGAAGAGGAG | 221178 |
rs57708966 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030089 | ACACACACACACACA[-/CA]TACATACATACATAC | 221178 |
rs57792784 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166845 | ATTAATCTCCTTCAC[A/G]AGAGGGGAGCCCTCA | 221178 |
rs57803066 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292229 | TACATTAGGCATGTC[A/T]CCCATTCAGCATTGG | 221178 |
rs57863513 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248883 | CTTTTTTTTTTTTTT[-/T]GAGAAAGAGCCGTGC | 221178 |
rs57947508 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248623 | AGTTCTTTGAATCCT[C/T]GTTCAGTGCTCGCCC | 221178 |
rs57970477 | in-del | -/ACTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046952 | GAACAGGAGTTTATT[-/ACTT]TATTACTCAAATCAG | 221178 |
rs58132107 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280664 | CATCAGGATATCTCG[A/G]CCAGTAAGCAGCACA | 221178 |
rs58132571 | snp | G/T | 0.00459863 | 0.0477301 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288954 | TACTATTCAAATAAT[G/T]TATTTGGATTTCCAA | 221178 |
rs58142582 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030062 | AACACACACACACAC[A/G]CACGCACACACACAC | 221178 |
rs58183046 | snp | C/G | 0.340784 | 0.232934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028946 | TTTTATAATCTACAT[C/G]TAATAATTTTACTTC | 221178 |
rs58212859 | snp | C/T | 0.093417 | 0.194889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011202 | CTTGCCTGGGTGCCA[C/T]CTCCCAGCCTGGATC | 221178 |
rs58225849 | in-del | -/TC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271009 | CTCTCTCTCTCTCTC[-/TC]CACTCTCTCTCACTC | 221178 |
rs58260888 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998304 | ATCTTGGAGTAGTTT[A/T]AATTTGCATTTTCTT | 221178 |
rs58330072 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285262 | CAATTGCTGTAAAGT[A/G]TAAAGTTAGATGCAA | 221178 |
rs58421689 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142122 | AGGTTTTTTTTTTTT[-/TT]AGCTTTTTTATGCTA | 221178 |
rs58570166 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143211 | AGAGAAAGCCTGCAG[A/C]CAAGGAGTCAGTGGG | 221178 |
rs58584983 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24249080 | TCTGCATGTTGCCCA[A/G]GCTGGTCTTGAACTC | 221178 |
rs58600844 | in-del | -/T/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046309 | TGCCTTTTTTTTTTT[-/T/TT]AAGAGTCAGAGTGTC | 221178 |
rs58617156 | snp | A/T | 0.155325 | 0.23138 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107774 | CTCTTTCTGTTTTAG[A/T]CTTTGGTGGGAACTC | 221178 |
rs58632380 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299213 | CCAAAGACGGCACTA[G/T]TTAGTGGGGGCATCC | 221178 |
rs58659073 | in-del | -/A | 0.370974 | 0.218781 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258236 | GTGAAACTCTATCTC[-/A]AAAAAAAAAAAATAA | 221178 |
rs58665180 | snp | A/T | 0.117886 | 0.21224 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201808 | TATTTACCATTATGA[A/T]GTTGTACAAATAGTA | 221178 |
rs58706195 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173509 | TCCCCCCCGTCCCCC[A/C]ACTTTTTTTTTTTTT | 221178 |
rs58718429 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128751 | AAAAAAAAAAAAAAA[-/A]CTGCTTACTTCCCTT | 221178 |
rs58719636 | in-del | -/GT | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979308 | TGTGTGTGTGTGTGT[-/GT]CCTTGCTGCCTGAGG | 221178 |
rs58724994 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199132 | GAGCTCAAGCGATCC[A/G]CCCGTCTTGGCCTTC | 221178 |
rs58744273 | in-del | -/A | 0.300926 | 0.244758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206891 | AAAAAAAAAAAAAAA[-/A]GATACATGCATGCAT | 221178 |
rs58760424 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065615 | CTCACAAGACAGAGA[G/T]AGACGTCCCCTAAGC | 221178 |
rs58768380 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143555 | AAAAATGTGTTTTCT[A/G]ACTTAAAAAGTTGCT | 221178 |
rs58776942 | snp | C/T | 0.284733 | 0.247575 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053000 | CTCTAATTCCCAATT[C/T]TCTTGGATTTTCTCT | 221178 |
rs58789886 | in-del | -/TT | 0.398534 | 0.201091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210779 | GGGTTTTTTTTTTTT[-/TT]GTATTTCATTGGAAT | 221178 |
rs58865453 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24183621 | TGAGATTTCTTTACA[-/T]TTTTTTTTTTTTTTT | 221178 |
rs58889617 | snp | A/G | 0.000408907 | 0.0142929 | missense | SPATA13 | GRCh38.p7 | 13:24286220 | TCCTTTCAGCTGATC[A/G]GTGATGGCAACGTGG | 221178 |
rs58953154 | snp | C/T | 0.00244109 | 0.0348509 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286957 | ATCTGTGAGGTGGGA[C/T]GCCAGGCTGGGACCT | 221178 |
rs58960118 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141566 | ATATTCCTCTGTTAT[A/C]GAGCTTATCCAGATA | 221178 |
rs59058768 | snp | G/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065373 | ATGTGTGGGAGGGCT[G/T]TGAGCCTGCTTATGT | 221178 |
rs59067426 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254406 | CTGCTTCAGAGCTTG[C/T]GTCCCATCCAGGGCA | 221178 |
rs59069442 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193941 | TGAGTTTAGAAGGGT[A/G]GAAGCTTTGAGGACT | 221178 |
rs59094953 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24093972 | AGATGTCATTGTGCA[A/G]TAATGATGCTGTAGG | 221178 |
rs59116361 | snp | A/G | 0.11228 | 0.208646 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186772 | ATGGGCAACAACGCT[A/G]TTGAGGCGGTTGATC | 221178 |
rs59130588 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013707 | CTTTTTTTTTTCCAC[-/TT]TTTTTTTTTTTTTTG | 221178 |
rs59147518 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24168848 | CATTTTAATTTTAAA[A/T]ATTTGAAGTTAAATA | 221178 |
rs59161697 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287971 | GTCAGAGAACTGCCC[A/G]TTCTCTAATCGGATT | 221178 |
rs59307721 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062435 | TTCTTCTCCAATGGC[A/G]CCAGGGTGCACGGTG | 221178 |
rs59314499 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201067 | ACACACACACACACA[-/CA]GAGTTTGGATTTTGA | 221178 |
rs59337794 | in-del | -/AAAAAA/AAAAAAAAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999389 | AAAAAAAAAAAAAAA[-/AAAAAA/AAAAAAAAA]GCCTGTTCGGATATT | 221178 |
rs59393770 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113915 | AAAATATAGTTATAT[A/G]AACACCAACAGAAGT | 221178 |
rs59396217 | in-del | -/A/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24219021 | AAAAAAAAAAAAAAA[-/A/AA]GTTTCATTCTAAAGT | 221178 |
rs59428885 | snp | A/T | 0.275197 | 0.248727 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275968 | TGTTTTTTCCACACC[A/T]ATTTTTTCAACAAAA | 221178 |
rs59469081 | in-del | -/AGGGTTTGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052060 | CCTGTGTTTGGACGC[-/AGGGTTTGG]CTTCTTACACCAGCA | 221178 |
rs59585523 | snp | A/C | 0.316968 | 0.240864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141487 | ACTTACTCCTCAAAG[A/C]CTTCCTTGACTCCTC | 221178 |
rs59609838 | in-del | -/ATT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291746 | CTGTCTTTATTTTTT[-/ATT]TATTTTTTTATTTTT | 221178 |
rs59626805 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191530 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCTTGCTCT | 221178 |
rs59682217 | snp | G/T | 0.175897 | 0.238765 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135430 | GGTCCAGGTGCAGTG[G/T]CTCACGCCTGTAATC | 221178 |
rs59689324 | snp | A/G | 0.067446 | 0.170804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197303 | AATTGTAAAGCTGGA[A/G]AGAGTAAACAGTGCA | 221178 |
rs59696234 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062405 | GAGAGCTGAGGGCAC[A/C]CAGTCAGGATGAAAT | 221178 |
rs59725907 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24281134 | GCAACCGTCCCCTCT[C/T]CTTTAATGAGCAGGT | 221178 |
rs59784789 | snp | C/T | 0.23846 | 0.249734 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211815 | AAAGGCCTAGGCTCC[C/T]CCACCCTGTCCCTGC | 221178 |
rs59801219 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244184 | CCTTTCGTGTTTGTC[G/T]GTGTCCAAATTTCCC | 221178 |
rs59822745 | snp | C/T | 0.182296 | 0.240658 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279831 | ACTTTCCCTCGTCCA[C/T]GTTTCAAGTCTCTTG | 221178 |
rs59849427 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181986 | CGGATGTGGTGGCAC[A/T]CTCCTAAAATCCCAG | 221178 |
rs59906180 | in-del | -/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027152 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTAGC | 221178 |
rs59945310 | snp | A/G | 0.133435 | 0.221162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130552 | AACTCATTGTTTAGC[A/G]TCATGGGAACAAGGC | 221178 |
rs59950714 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24080947 | AAACACACGTACCTC[C/T]TAATAAGTTCCCAAT | 221178 |
rs59988914 | in-del | -/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148367 | TTTTTATTTTTTTTT[-/T]CCTGAAATGCATACA | 221178 |
rs59995344 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197375 | TCAAATTGTTAAAAC[A/G]TAACTATCTCTTAAA | 221178 |
rs60013392 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043027 | AGTGAATAATGCCAG[C/T]ATTGGCTCAGTTGAG | 221178 |
rs60017658 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144059 | CTCCCACCACACCCC[C/T]GACTGTGAATGTTCA | 221178 |
rs60047720 | in-del | -/AG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182494 | GAGAGAGAGAGAGAG[-/AG]CGCAGGAAAGAGGAT | 221178 |
rs60059042 | in-del | -/A | 0.084728 | 0.187577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096441 | AAATACAAAAAAAAA[-/A]TAGCTGGGCGTGGTG | 221178 |
rs60133037 | snp | C/T | 0.274661 | 0.248781 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275934 | GCAAGACCTTGTCCC[C/T]CACCCCTCCCCCAAA | 221178 |
rs60152605 | in-del | -/TT/TTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181774 | ACTTTTTTTTTTTTT[-/TT/TTT]GTTAAAGTAAGTAAG | 221178 |
rs60187376 | snp | G/T | 0.0923359 | 0.194016 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159132 | ATTTAGACCGTGATA[G/T]TTTTTTTTAAATAAT | 221178 |
rs60223356 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278986 | TCCCTCCCTCCCTCC[C/T]TCCCTCCCTTCCTTC | 221178 |
rs60268646 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140277 | TAATCTGTGAACACC[A/G]CGGTGGGTTCTGGGG | 221178 |
rs60287370 | in-del | -/TGTA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067342 | CCTGAGCTATATGTA[-/TGTA]CCCTTTGTAAGTCAA | 221178 |
rs60287491 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24298189 | AGAGATGGAACCCCA[C/T]TATGGTGACCATCAC | 221178 |
rs60332756 | snp | C/G | 0.226484 | 0.248892 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192395 | CTCTGCTTGGTGACT[C/G]TGATGCCTGCTACTC | 221178 |
rs60365334 | snp | A/T | 0.125528 | 0.21681 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113859 | TGGCGACAGAGTGAG[A/T]CTCGATCTCAAAAAA | 221178 |
rs60376551 | snp | C/G | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254201 | ATTCACTGTGGCCAG[C/G]ACTGTGAACTCTGGA | 221178 |
rs60387853 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245296 | CTTAAAAAAAAAAAA[-/A]GATTCCATTTTAGAA | 221178 |
rs60404353 | snp | A/G | 0.112631 | 0.208878 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186809 | AAGAGAAAAGGGAAG[A/G]AAGAGCTGGAAATAG | 221178 |
rs60416353 | in-del | -/T | 0.499902 | 0.00698814 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993998 | TTTTTTTTTTTTTTC[-/T]TTTTTTTTTTTTGAC | 221178 |
rs60421563 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229553 | TGGTTATCACTGTTT[A/G]GATGATTTTTCCATC | 221178 |
rs60448670 | in-del | -/ACTCTGCT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112322 | CTGGGTCAGTTTGCT[-/ACTCTGCT]CTTGTTGCCCCTACA | 221178 |
rs60451001 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185393 | TCCTGATTCAAGACT[-/GT]AATTTATTCTTAAGC | 221178 |
rs60473362 | in-del | -/AAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236612 | AAAAAAAAAAAAAAA[-/AAA]GATATGCAAATGATA | 221178 |
rs60474013 | snp | G/T | 0.143284 | 0.226079 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005206 | TTGCAAATCAGTTCT[G/T]TTTTCTGGTAGCCTG | 221178 |
rs60487326 | in-del | -/GTTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025192 | TATTTTCCTATTTTT[-/GTTT]ATTTCCTAAAATTTT | 221178 |
rs60492187 | in-del | -/GTCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024455 | TCTCTTGGGTTGTCT[-/GTCT]AGTGACAAGACCAAC | 221178 |
rs60512918 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292329 | AAGGTAGCAGTGCTT[A/G]GCTAATTCTGAGTTC | 221178 |
rs60596587 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057031 | TCTCTCTCTCTCTCT[-/CT]TTCTTTCATAGCGTC | 221178 |
rs60624538 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119198 | AGGCGTGAGCCACCG[C/T]GCCCGGCTGACACTA | 221178 |
rs60679290 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24071014 | TCTACGTCTGTGTTA[-/A]TGTCTATATCTGTGT | 221178 |
rs60681041 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169113 | GATTAGCCTGGCATT[-/T]GGGATCTCTGCGTGT | 221178 |
rs60684852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063238 | TTGCCAAACCACCAT[A/G]GGCACAAAGAGAGCA | 221178 |
rs60692760 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101497 | TGTGGTGAAAAAAAA[A/C]AACACATAAAACTTA | 221178 |
rs60700892 | in-del | -/AT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038362 | AGTTCCCTCTGTTCT[-/AT]GTTTACATTGGAGTC | 221178 |
rs60704968 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274856 | GTCGGGAACCAGCTG[C/T]TCATTAGCTAGGCAG | 221178 |
rs60729543 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237254 | CCCAGCTACTCAGGA[A/G]GTGGAGGCTGAGGCA | 221178 |
rs60739293 | in-del | -/TT | 0.441843 | 0.160301 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183606 | TGAGATTTCTTTACA[-/TT]TTTTTTTTTTTTTTA | 221178 |
rs60767861 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085487 | CAGAGGGGCAGTGCC[A/G]TCTGGAAGCCCTGCC | 221178 |
rs60786196 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992793 | CTTGGGGACATGGCC[A/G]CGTTTGGCTCCACAA | 221178 |
rs60788782 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153581 | AGGACACGTGGTAGA[C/G]AGAATGATCCACGGT | 221178 |
rs60810328 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077286 | AAAAAAAAAAAAAAA[-/A]GAGCCCAGTCCACAA | 221178 |
rs60850610 | in-del | -/TGTGTGTG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173395 | GTGTGTGTGTGTGTG[-/TGTGTGTG]GTAGATTTCTTGAGA | 221178 |
rs60927394 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170640 | AATTGGAACACCTGT[-/GT]CTCCTGAGATGAAGA | 221178 |
rs60944179 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202521 | CTTTCTTTCTTTCCC[C/T]TTTTTTTTTTTTTTT | 221178 |
rs60948401 | in-del | -/TTACT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232371 | CAAGTCTTCTTTACT[-/TTACT]GATTACTGATTCCAA | 221178 |
rs60974700 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24284187 | GGATGACAACGGTAG[C/T]GAGGAGGACTTCAGC | 221178 |
rs61044216 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199820 | GCTTTTGTTTGTCAA[G/T]TGTTCCCACTAAGCC | 221178 |
rs61057177 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291748 | TGTCTTTATTTTTTT[-/A]TTTTTTTATTTTTTT | 221178 |
rs61071711 | snp | A/G | 0.39214 | 0.205661 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004281 | GTCAATAAAGAGTCA[A/G]GAGTGAAATCCCGGT | 221178 |
rs61083651 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106153 | ACCCTCCTGCCCCAG[C/T]CTCCCAAGTAGCTTG | 221178 |
rs61136651 | in-del | -/GGTGAGCCTCGGCTGGTGA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015798 | GCCAAACCATGCCAA[-/GGTGAGCCTCGGCTGGTGA]CACGTCATAGTCCCC | 221178 |
rs61153723 | in-del | -/TTTTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025823 | TCTTTCTTTTTTTTT[-/TTTTT]GAGACGGAGTCTCAC | 221178 |
rs61170395 | snp | C/T | 0.211516 | 0.24702 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281141 | TCCCCTCTCCTTTAA[C/T]GAGCAGGTAAGAAAG | 221178 |
rs61191748 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24264089 | ATCATCGAGATTTTT[-/T]AGAAGGAATATAGTG | 221178 |
rs61192628 | snp | C/T | 0.354665 | 0.227036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177186 | AATAGTGGACACAAA[C/T]GTTGCTTTACTTCTC | 221178 |
rs61198710 | in-del | -/ACTAAGGAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064996 | CACAGGCCACAGGAG[-/ACTAAGGAG]CCAGGATAATGAAAT | 221178 |
rs61215087 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290526 | ATTTCATGCCCTGTC[C/T]TTCTTGCAGTAGTCC | 221178 |
rs61250549 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128015 | ACCCATGTGCCACAC[A/T]ATGATCTTTTGATGT | 221178 |
rs61296399 | in-del | -/CGTGATCCGCCCT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026812 | TGGATCTCCTGACCT[-/CGTGATCCGCCCT]TGTGATCCTGACCTT | 221178 |
rs61316306 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245608 | TTTTTTTTTTTTTTT[-/T]AGACAACAGGTCTTG | 221178 |
rs61369469 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154636 | ACAGTGTGTTAAAAA[-/A]CTATGCACATTTATT | 221178 |
rs61414133 | in-del | -/AA/AAA | 0.16028 | 0.233346 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206873 | TCCAGCCTGGGCAAC[-/AA/AAA]GAGTGAAACTCTGTC | 221178 |
rs61484696 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173512 | CCCCCGTCCCCCAAC[C/T]TTTTTTTTTTTTTGG | 221178 |
rs61485171 | in-del | -/TTATTTTTTATTTTTTATTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291755 | TTTTTTTATTTTTTT[-/TTATTTTTTATTTTTTATTTTTT]ATTTTTTTTTTTGAG | 221178 |
rs61523191 | in-del | -/T | 0.305934 | 0.243663 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983235 | AGTCTGCAGGGATGG[-/T]TTTTTTCTGACGCCG | 221178 |
rs61559266 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106335 | ACCTTACCTGGCCTA[A/C]GATTTCTAATTAAAA | 221178 |
rs61569616 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279540 | CAGGCTTAAGTGGTG[A/G]GAGGGGACCCAGGCT | 221178 |
rs61625532 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237623 | GGTGGTGATAATTAC[A/G]TAACAGTGTGAATGT | 221178 |
rs61641076 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098942 | AAAAAAAAAAAAAAA[-/A]GAAAAAAGAATTAGC | 221178 |
rs61945305 | snp | A/C | 0.412249 | 0.190198 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997552 | ATTAGTCCATTTTGC[A/C]TTGCTATAGAGAAAT | 221178 |
rs61945306 | snp | G/T | 0.412249 | 0.190198 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997555 | AGTCCATTTTGCATT[G/T]CTATAGAGAAATACC | 221178 |
rs61945307 | snp | C/T | 0.409721 | 0.192325 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997557 | TCCATTTTGCATTGC[C/T]ATAGAGAAATACCTG | 221178 |
rs61945308 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000409 | AAAGACAGTGCTGGG[C/T]GGTGAGGTGTCTAAG | 221178 |
rs61945309 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013078 | CACTGGCTGCAGCCC[A/G]TGTGGCTGAGCCCAG | 221178 |
rs61945310 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013505 | TACTCTGAGAATGGG[A/G]ACAAGAAATCTACAC | 221178 |
rs61945332 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026285 | AAGTCACATAGCTAC[A/C]CTCCTCTGTTTTCTG | 221178 |
rs61945344 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044231 | TTTGTTTTTCTTTCT[C/T]TCTTTTTTTTTTTTT | 221178 |
rs61945347 | snp | A/G | 0.106278 | 0.204558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053387 | CCATGGCTGATTCAC[A/G]TGGAGTTCCTGCATA | 221178 |
rs61945349 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058344 | GTTTAAACCCCCTTA[A/G]TTATATCAACTCATT | 221178 |
rs61945461 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068871 | ATGAAGTTTTTTCTT[C/G]TAAATGTGTTTAAGT | 221178 |
rs61945462 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068877 | TTTTTTCTTGTAAAT[G/T]TGTTTAAGTTCCTTA | 221178 |
rs61945463 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068880 | TTTCTTGTAAATGTG[C/T]TTAAGTTCCTTATAG | 221178 |
rs61945464 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068893 | TGTTTAAGTTCCTTA[C/T]AGATGCTGGATATTA | 221178 |
rs61945466 | snp | A/G | 0.181978 | 0.240568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079207 | TAGATGGCCCACATG[A/G]CTGCAGGAGAGACTT | 221178 |
rs61945476 | snp | A/T | 0.125874 | 0.217008 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090332 | AGCTTCCCCTTTCAT[A/T]GCTCCAGCCCATCCC | 221178 |
rs61945477 | snp | C/T | 0.125874 | 0.217008 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090839 | CATGGAACTAAACTT[C/T]CCTGTTTCTTTTCAT | 221178 |
rs61945478 | snp | C/G | 0.126219 | 0.217206 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091010 | TCATTTGTAGCTCCC[C/G]AAGTCTCTGCTTAGT | 221178 |
rs61945479 | snp | A/G | 0.110872 | 0.20771 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092007 | TGCCACAAAATCACC[A/G]TTCTTCCTGACGGTT | 221178 |
rs61945480 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098825 | CTAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 221178 |
rs61945481 | snp | A/C | 0.109461 | 0.206758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101469 | GTGTATTCAATTTAA[A/C]TATTTTTTAAATTGT | 221178 |
rs61945506 | snp | C/T | 0.463234 | 0.130503 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103137 | GGCAGAAGAATCTCA[C/T]GAACTTCACTTTAAA | 221178 |
rs61945508 | snp | A/G | 0.117886 | 0.21224 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119176 | CCTCCCAAAGAGCTG[A/G]GATTACAGGCGTGAG | 221178 |
rs61945509 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120799 | CCAGGTGTTTTCATT[A/G]CCTACCAGGTACTTA | 221178 |
rs61945510 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138905 | CCTAAAATATCTTTT[A/C]ATATCCTTCATCTAG | 221178 |
rs61945520 | snp | A/G | 0.17138 | 0.237316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144566 | CCCAGACAAACTTTG[A/G]TCAGGCACCGCTGAG | 221178 |
rs61945542 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173527 | TTTTTTTTTTTTTTG[G/T]CCTTATTGCATTGGC | 221178 |
rs61946653 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182494 | GAAGTGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA | 221178 |
rs61946654 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189494 | CTCTCTATATATATA[C/T]GTGTATATATATATA | 221178 |
rs61946655 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189497 | TCTATATATATACGT[A/G]TATATATATATATAA | 221178 |
rs61946656 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190281 | ATATATTATTATATA[A/T]AATATATAATATTAT | 221178 |
rs61946657 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190282 | TATATTATTATATAT[A/C]ATATATAATATTATA | 221178 |
rs61946658 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190293 | ATATAATATATAATA[A/T]TATATATTATTATAT | 221178 |
rs61946659 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190310 | ATATATTATTATATA[A/T]AATATATAATATTAT | 221178 |
rs61946671 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219002 | AAATTCTCATTATCA[A/C]CAAAAAAAAAAAAAA | 221178 |
rs61946672 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24219165 | GACTTGCTACAAAAC[A/C]ACTAATTGAATTGCA | 221178 |
rs61946674 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230367 | ATGAGAATGCAGTAA[G/T]TGCCGCAGGAGCCCC | 221178 |
rs61946676 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233640 | TTAAAAAAAAAAGTT[A/T]CCATTTGCTCTGAAA | 221178 |
rs61946696 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24279498 | CAGGAGGGGCTGCTG[G/T]AGGGAGCCCGAAGCT | 221178 |
rs61946698 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293952 | CTGTGCTGTAAGTTG[A/C]CACGGGAAAGCGGAA | 221178 |
rs61946749 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295676 | CAAATTCTCACTCTC[A/T]CTCTCTCTCTCTCTC | 221178 |
rs61946750 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301596 | TTCACAGGTGGCTAC[C/T]GGGTGGGACGCTGTG | 221178 |
rs61948460 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190322 | ATATAATATATAATA[A/T]TATATATTATTATAT | 221178 |
rs61948461 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190339 | ATATATTATTATATA[A/T]AATATATAATATTAT | 221178 |
rs61948462 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190340 | TATATTATTATATAT[A/C]ATATATAATATTATA | 221178 |
rs61948463 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190351 | ATATAATATATAATA[A/T]TATATATTATTATAT | 221178 |
rs61948464 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190366 | TTATATATTATTATA[C/T]ATAATATATAATATT | 221178 |
rs61948465 | snp | A/G | 0.450859 | 0.148847 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190376 | TTATATATAATATAT[A/G]ATATTATATATATAA | 221178 |
rs61948466 | snp | C/G | 0.408644 | 0.203363 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190447 | TCTGGGCAAAGTAAA[C/G]TGAAAACCTTCTGGA | 221178 |
rs61948467 | snp | A/T | 0.431916 | 0.171483 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191599 | ACTGCAAGCTCTGCC[A/T]CCTGGGTTCACGCCA | 221178 |
rs61948481 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198636 | TGTTGATTGGAATTT[A/G]AAACTCTATGTATGT | 221178 |
rs66531229 | in-del | -/CTCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295671 | TCCAACAAATTCTCA[-/CTCT]CTCTCTCTCTCTCTC | 221178 |
rs66540663 | in-del | -/A/AA/C | 0.625 | 0.125 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103502 | AAAAAAAAAAAAAAA[-/A/AA/C]CAAGAAAGAAAAGAG | 221178 |
rs66694707 | snp | C/G | 0.237014 | 0.249662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120717 | TTGTTATTACAAAAG[C/G]TTAAAATCAAAATTA | 221178 |
rs66740821 | in-del | -/ACTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037401 | AGGTTCTCGACTAAT[-/ACTT]TATTTATTTATTTAT | 221178 |
rs66810619 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238133 | TTTTTTTTTTTTTTT[-/T]GAGACAGACTCTTGC | 221178 |
rs66877108 | in-del | AG/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042446 | TGCTTCTGTTTCCAA[AG/T]CAAACCAGGCTGCTG | 221178 |
rs66939803 | in-del | -/GA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182496 | GAGAGAGACAGAGAG[-/GA]AGAGAGAGAGCGCAG | 221178 |
rs66985719 | in-del | -/T | 0.498034 | 0.0312882 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043321 | TGGTGGATGCTACCC[-/T]TTTTTGTGGTCAAAC | 221178 |
rs66989251 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042447 | GCTTCTGTTTCCAAA[-/G]CAAACCAGGCTGCTG | 221178 |
rs67025379 | in-del | -/T | 0.404209 | 0.196773 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253465 | CCTCTTCAGCGTTGA[-/T]TAACTAGAGGCAGAT | 221178 |
rs67102450 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240995 | CTTTTTTTGTTTTTT[-/T]GGAGACTCTTTAAAA | 221178 |
rs67117888 | in-del | -/A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117684 | AAGAGAAATTAAGAG[-/A/G]AAAAAAAACCCCAAA | 221178 |
rs67125164 | in-del | -/TAAATAAATAAATAAATAAATAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202071 | GAGCAAGACTCTGTC[-/TAAATAAATAAATAAATAAATAAA]TAAATAAATAAATAA | 221178 |
rs67188496 | in-del | -/GTGTATGTATGTATGT | 0 | 0 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269390 | TGTATGTATGTATGT[-/GTGTATGTATGTATGT]ATCTATTTTAGAGAC | 221178 |
rs67290990 | in-del | -/T | 0.0685596 | 0.171987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264427 | GAAATATTCGGTAAC[-/T]TTTCCTAGCTTGGCT | 221178 |
rs67348620 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118912 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTGAGA | 221178 |
rs67373067 | in-del | -/GAT/TGA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996617 | CTGTGCTTGGCTGAT[-/GAT/TGA]TGGCTGAGATTTGGC | 221178 |
rs67451961 | in-del | -/T | 0.440884 | 0.161442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280491 | TTTTTTTTTTTTTTT[-/T]GGCTCAACCACGGTT | 221178 |
rs67477021 | multinucleotide-polymorphism | CATA/TAAC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190366 | ATATATATTATTATA[CATA/TAAC]ATATATGATATTATA | 221178 |
rs67518255 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277463 | AAAAAAAAAAAAAAA[A/G]AAGAAGTTCACCTTG | 221178 |
rs67518708 | in-del | -/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052492 | AAAAAGAAATATATG[-/T]TTTTTTTTTTCTTTT | 221178 |
rs67529288 | in-del | -/TGCTACTC | 0.476918 | 0.104919 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112318 | CTCACTGGGTCAGTT[-/TGCTACTC]TGCTCTTGTTGCCCC | 221178 |
rs67549120 | in-del | -/A | 0.0705549 | 0.174067 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135219 | TACACTCATTATTCG[-/A]AAAAAAAAATACTTT | 221178 |
rs67589784 | in-del | -/G | 0.0818113 | 0.184966 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002959 | TCTTTTTCTGAATGT[-/G]GGGGGTGAACAGAGA | 221178 |
rs67688298 | in-del | -/G | 0.412249 | 0.190198 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997550 | ATATTAGTCCATTTT[-/G]CATTGCTATAGAGAA | 221178 |
rs67709070 | in-del | -/T | 0.494013 | 0.0543839 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044234 | GTTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 221178 |
rs67729020 | in-del | -/T | 0.123452 | 0.215605 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201452 | CATTAGAGTTCACTC[-/T]TTTTTTTGAGACAGA | 221178 |
rs67779646 | in-del | -/A | 0.0858192 | 0.188533 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084544 | TTTCTGGTTTTTCTT[-/A]AAAAAAAGCAACACT | 221178 |
rs67825868 | in-del | -/T | 0.067446 | 0.170804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196846 | ATGGAGAGTAGTACA[-/T]TTCAAGAGATAAGGA | 221178 |
rs67940479 | in-del | -/T | 0.150333 | 0.229274 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304460 | ATGCTATCCCTGCAG[-/T]TTTTTTTTTTCTAAC | 221178 |
rs68080717 | in-del | -/CC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116770 | TTGAAGCCCTACCAG[-/CC]CCCCCCCCCCAATGT | 221178 |
rs68108344 | in-del | -/T/TT/TTT | 0.0930568 | 0.194599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046298 | TAGATTTCTTTTGCC[-/T/TT/TTT]CTTTTTTTTTTTAAG | 221178 |
rs71070644 | in-del | -/GGAT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024357 | GATGAATGGATGGAC[-/GGAT]GGATGGATGGATGGA | 221178 |
rs71070647 | in-del | -/T/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044234 | GTTTTTCTTTCTTTC[-/T/TT]TTTTTTTTTTTTTTT | 221178 |
rs71070648 | in-del | -/CAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052397 | CAACAACAACAACAA[-/CAA]ACTATTATTTAAAAA | 221178 |
rs71070649 | in-del | -/T/TT | 0.438246 | 0.16451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052491 | TATGTTTTTTTTTTT[-/T/TT]CTTTTAAACCCATGA | 221178 |
rs71070651 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090126 | CCTTTATTTTTTTTT[-/T]CTTCTAAATCTGGCA | 221178 |
rs71070652 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098602 | TAAAAAAAAAAAAAA[-/A]GAAGAAGAAGAAAAG | 221178 |
rs71070653 | in-del | -/GAAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098638 | AAAGAAAGAAAGAAA[-/GAAA]AAAGAAAGGGCCGGA | 221178 |
rs71070656 | in-del | -/T/TT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185734 | GCAGTTTTTTTTTTT[-/T/TT]CATGAGCCCTGTGTT | 221178 |
rs71070657 | in-del | -/AG/GA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185819 | AGAGAGAGAGAGAGA[-/AG/GA]TTAAGGAATTGGCTC | 221178 |
rs71070659 | in-del | -/ATATTATATATTATATATTTATATATTATATATATT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189646 | TATATATTTATATAT[lengthTooLong]TATATATATTATATA | 221178 |
rs71070662 | in-del | -/ACATATGATATATAATATATA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190357 | ATATATTATTATATA[-/ACATATGATATATAATATATA]TTATTATACATAATA | 221178 |
rs71070663 | in-del | -/A | 0.449345 | 0.150869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190404 | AATAAGGCTGTAGTT[-/A]ACCATGGATGGTGAT | 221178 |
rs71070664 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191502 | CTATACATTGCTTTC[-/T]TTTTTTTTTTTTTTT | 221178 |
rs71070666 | in-del | -/ACATGTTTAAATATGCAATATATAAACAT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237958 | GCAATATATAAACAT[lengthTooLong]GTATAATATATATAT | 221178 |
rs71070671 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258242 | TCTATCTCAAAAAAA[-/A]AAAAAATAAAAAGAA | 221178 |
rs71070673 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269742 | TTTTTTTTTTTTTTT[-/T]AGTAGAGACAGGACC | 221178 |
rs71070674 | in-del | -/TC | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271040 | CTCTCTCTCTCTCTC[-/TC]ACTCTCTCTCTCTCT | 221178 |
rs71070675 | in-del | -/GTTTCTCTGAGAGGGGCACCCCAGGCAG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281665 | GGGCACCCCAGGCAG[-/GTTTCTCTGAGAGGGGCACCCCAGGCAG]AGGGGGAAGCAACTG | 221178 |
rs71070676 | in-del | -/TTT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291767 | TTTATTTTTTTTTTT[-/TTT]GAGACGGAGTCTCGT | 221178 |
rs71070677 | in-del | -/CTCT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295697 | TCTCTCTCTCTCTCT[-/CTCT]GTATTCATAAAAACA | 221178 |
rs71070678 | in-del | -/AAAAAAAAAA | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302480 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GAATTAGCTGAGAAC | 221178 |
rs71186804 | in-del | -/TGTGCCCAGAGTAGCC | 0.475702 | 0.107512 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987077 | CTACCCCATAGGCAG[-/TGTGCCCAGAGTAGCC]TGGATTGATATTTTA | 221178 |
rs71186805 | multinucleotide-polymorphism | AT/TG | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006853 | AGGGAAGCCACGTCG[AT/TG]GGTGTAGGGGGAGAG | 221178 |
rs71186807 | in-del | -/ATCCAA | 0.496681 | 0.0405994 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060701 | TGACAAAGGTCTAAT[-/ATCCAA]ATCCAGCATCTGTAA | 221178 |
rs71186809 | in-del | -/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089245 | GGCCAGCCTCTGCTT[-/C]CATGGTTTGCTGTTC | 221178 |
rs71186810 | in-del | -/AC/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098607 | TTAAAAAAAAAAAAA[-/AC/C]AAGAAGAAGAAGAAA | 221178 |
rs71186811 | in-del | -/A | 0.224116 | 0.248656 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098925 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs71186812 | in-del | -/AG | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108659 | GCTGCTTTTCATGGT[-/AG]AGGGGCGGGGGGAAG | 221178 |
rs71186813 | in-del | -/TG | 0.347253 | 0.230308 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170639 | GTGAATTGGAACACC[-/TG]TGTCTCCTGAGATGA | 221178 |
rs71186817 | multinucleotide-polymorphism | AC/GT | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212438 | TCCTTGCTTCATGTG[AC/GT]CCTGAAGTGCTTATG | 221178 |
rs71186818 | in-del | -/TTTTTTT | 0.40157 | 0.198813 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228109 | TCCCCTCTTGTACTC[-/TTTTTTT]TTTTTTTTTTTTTTT | 221178 |
rs71186819 | in-del | -/ACACACAC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233887 | ACTTTATACACTTAA[-/ACACACAC]ACACACACACACACA | 221178 |
rs71186820 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258235 | GTGAAACTCTATCTC[-/A]AAAAAAAAAAAAATA | 221178 |
rs71186821 | in-del | -/T/TT | 0.234692 | 0.249531 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262309 | ACAAAGTTTTTTTTC[-/T/TT]TTTTTTTTTTTTTAG | 221178 |
rs71186822 | in-del | -/ATGAAG | 0.368119 | 0.220336 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277518 | GAGGGAAACAGAGTC[-/ATGAAG]ATGAAGACTGGCTGA | 221178 |
rs71186823 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292996 | GTGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs71218555 | in-del | CTG/TGGTGTCCTC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042126 | TTTGCTGAGAAAGCG[CTG/TGGTGTCCTC]TGTCCTCTGTGTCAC | 221178 |
rs71218556 | multinucleotide-polymorphism | CCC/TCT | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109351 | ATTTTCTTAATCCGG[CCC/TCT]ATCATTGATGGGCAT | 221178 |
rs71225272 | in-del | -/AGAA | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098637 | GAAAGAAAGAAAGAA[-/AGAA]AAAAGAAAGGGCCGG | 221178 |
rs71425114 | snp | C/G | 0.34146 | 0.23267 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190247 | TATTATATAACATAT[C/G]ATATATAATATACAT | 221178 |
rs71425115 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190275 | TATTATATAACATAT[C/G/T]ATATATAATATATAT | 221178 |
rs71425116 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190319 | GATATATAATATATA[A/T]TATTATATAACATAT | 221178 |
rs71427398 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993986 | TTTTTTTTTTTTTTT[CT/TC]TTTTTTTTTTTGACA | 221178 |
rs71429868 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992069 | CCCTCACAAAACCTA[A/G]GAAGTGAGTTAGAAT | 221178 |
rs71429869 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035142 | ACTTATTGGGCATTG[G/T]TTACTTTCTATATGT | 221178 |
rs71429870 | snp | A/T | 0.117188 | 0.211804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057138 | CACAATGTGCAGGTT[A/T]GTTACATATGTATAC | 221178 |
rs71429871 | snp | A/G | 0.111928 | 0.208413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060900 | AAAAATTAGCTGGGC[A/G]TGCTAGTGCATGCCT | 221178 |
rs71429873 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093613 | GTGCTAAATGGACCA[A/G]TTGTGGGGAGAGGCA | 221178 |
rs71429874 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173406 | TGTGTGTGTGTGGTA[A/G]ATTTCTTGAGATTTT | 221178 |
rs71429875 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235904 | AGAATATAAATAATA[A/C]CAGCTCAAATTGATA | 221178 |
rs71429876 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277466 | AAAAAAAAAAAAAAA[A/G]AAGTTCACCTTGGAA | 221178 |
rs71705366 | in-del | -/TGTGCCCAGAGTAGCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987078 | TACCCCATAGGCAGT[-/TGTGCCCAGAGTAGCC]GGATTGATATTTTAA | 221178 |
rs71712571 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057058 | GCGTCTGGCTCTTTC[-/T]TTTTTTTTTTTCTTT | 221178 |
rs71721813 | in-del | -/TC | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057006 | TGTGGCTGTTTTCTT[-/TC]TCTCTCTCTCTCTCT | 221178 |
rs71748246 | in-del | -/AC/CA | 0.197075 | 0.244334 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043481 | CTTGATTGATATTAC[-/AC/CA]ACACACACACACACC | 221178 |
rs71757402 | in-del | -/C | 0.108048 | 0.20579 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090198 | TCTGCACTTGGACAT[-/C]CCCCTTATGGACTTT | 221178 |
rs71772290 | in-del | -/AGGTGAGCCTCGGCTGGTG | 0.474723 | 0.109542 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015797 | AGCCAAACCATGCCA[-/AGGTGAGCCTCGGCTGGTG]ACACGTCATAGTCCC | 221178 |
rs71898296 | in-del | -/T | 0.38555 | 0.210062 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983646 | ATATTCTGTTGGTTG[-/T]TTTTTTTTTTTAAAA | 221178 |
rs71915188 | in-del | -/TA/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019094 | TATTATTATTATTAT[-/TA/TTT]TTTTTTTTTTTTGAG | 221178 |
rs71928912 | in-del | -/CT | 0.109461 | 0.206758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271042 | TCTCTCTCTCTCTCA[-/CT]CTCTCTCTCTCTCTC | 221178 |
rs71948264 | in-del | -/ACAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24233887 | ACTTTATACACTTAA[-/ACAC]ACACACACACACACA | 221178 |
rs71974792 | in-del | -/AAGA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084099 | AGAGAAAGGGGGAGA[-/AAGA]GAGAGCCGTGACTAG | 221178 |
rs71995137 | in-del | -/T | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254199 | GATTCACTGTGGCCA[-/T]GGACTGTGAACTCTG | 221178 |
rs72004531 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983658 | TTGTTTTTTTTTTTT[-/A]AAAAACATCCAGAAC | 221178 |
rs72027768 | in-del | -/AT/TA | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237992 | TATAAACATGTATAA[-/AT/TA]TATATATATATAAAT | 221178 |
rs72180227 | in-del | -/AGAA | 0.134119 | 0.221521 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084096 | GAAAGAGAAAGGGGG[-/AGAA]AGAGAGAGCCGTGAC | 221178 |
rs72243336 | in-del | -/AGAGAGAGAGAGAGA | 0.102014 | 0.201495 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103529 | AGAGCAGGGGAGGAG[-/AGAGAGAGAGAGAGA]AGAGAGAGAGAGAGA | 221178 |
rs72310549 | in-del | -/ATATATATATAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024934 | AAAACATTCAAATTC[-/ATATATATATAA]ATATATATATAAATA | 221178 |
rs72389621 | in-del | -/CTT | 0.180064 | 0.240019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063126 | GCCTGGACCAGGCTC[-/CTT]CTCCCAGTGCTCACC | 221178 |
rs72411718 | in-del | -/TAAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048466 | TAGATCTAGTAAACT[-/TAAG]AATCAAGGATGAAGA | 221178 |
rs72511484 | in-del | -/CA/CC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207560 | CAGTACACCCGGGTT[-/CA/CC]CGTTTCTCCACATCC | 221178 |
rs72623414 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192385 | CTCCTTGCAGCTCTG[C/T]TTGGTGACTGTGATG | 221178 |
rs73162121 | snp | G/T | 0.100944 | 0.200705 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989789 | GAGGCCTTGGGAAGT[G/T]ATTAGATCATGAGGA | 221178 |
rs73162125 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993986 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTGAC | 221178 |
rs73162127 | snp | A/T | 0.0980852 | 0.198549 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995082 | CATCTCACCATACAC[A/T]GGACAGCCCCCAAAC | 221178 |
rs73162129 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996129 | CTGCTGTAACAAGTT[A/C]CCAGGAACCTAATGG | 221178 |
rs73162135 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000901 | GGTGAGGTGTGAATT[C/T]GGGAGATTCCCTGGG | 221178 |
rs73162147 | snp | A/C | 0.317451 | 0.240729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023360 | ATAGCTCAGTAAATT[A/C]ATTTCTCTGGAGTGA | 221178 |
rs73162150 | snp | A/G | 0.318174 | 0.240525 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023754 | CCAAGGAATGTGGGC[A/G]CCTCTCAAAGCTGGG | 221178 |
rs73162153 | snp | C/G | 0.132751 | 0.2208 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025032 | ATCTTAAGAAACAGA[C/G]TATTATAAAAATCTA | 221178 |
rs73162154 | snp | A/C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025231 | AAATGAATCAAATTT[A/C/G]TATGCATTCTCCTTC | 221178 |
rs73162156 | snp | A/G | 0.317933 | 0.240593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025430 | CAAAAATACTTTCCA[A/G]TGAACATTCTATGTG | 221178 |
rs73162159 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026164 | CAAAGTATGATTTTT[A/C]ATGTCGTTTTATGGT | 221178 |
rs73162165 | snp | A/G | 0.31721 | 0.240796 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028720 | ATTGAATGTTTGTCC[A/G]TTCTTACGCTTCAAG | 221178 |
rs73162166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029189 | TAGCCTCCCAAGTAG[C/T]TGGAACTTACAGGCA | 221178 |
rs73162170 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031356 | GACTCTAGCACACCA[A/G]TTCATGCTAGCACAT | 221178 |
rs73162175 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033872 | TTTTTGGCTATTAGA[C/G]CTTATTTGGCTTTTA | 221178 |
rs73162176 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033873 | TTTTGGCTATTAGAG[C/T]TTATTTGGCTTTTAT | 221178 |
rs73162199 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042630 | TCAGCTGGTGTATTC[A/T]TTACCAGGGGGTAAA | 221178 |
rs73162202 | snp | A/G | 0.209084 | 0.246629 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042954 | TATAAAAATACCTCC[A/G]TAAATATATCCTCAA | 221178 |
rs73164008 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050553 | AGGAGGGACCCAGCT[A/G]GCATGTGGCTGGAGC | 221178 |
rs73164010 | snp | A/G | 0.21303 | 0.247251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051776 | GCAGCAGTGCTATCA[A/G]AAGTCTAGGCTGCAA | 221178 |
rs73164058 | snp | C/T | 0.462363 | 0.131916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103247 | AAACCAGGTTATTAC[C/T]AGTTTATTTTCTTTA | 221178 |
rs73164059 | snp | A/G | 0.462691 | 0.131387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103248 | AACCAGGTTATTACC[A/G]GTTTATTTTCTTTAC | 221178 |
rs73164064 | snp | A/G | 0.140919 | 0.224948 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103544 | AGAGAGAGAGAGAGA[A/G]GAGAGAGAGAGAGAA | 221178 |
rs73164074 | snp | A/C/G/T | 0.444444 | 0.157135 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116780 | ACCAGCCCCCCCCCC[A/C/G/T]CAATGTGCTGATGTT | 221178 |
rs73164084 | snp | C/G | 0.040671 | 0.13668 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129302 | AGCATGAGGGAAAGG[C/G]AATCCCAGATCTGAC | 221178 |
rs73164086 | snp | A/G | 0.040671 | 0.13668 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130029 | GGTGAGGTAGCCAGG[A/G]GGCTACTCCACACAG | 221178 |
rs73164095 | snp | A/G | 0.251296 | 0.249997 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137279 | AAGAAGAAGACATGG[A/G]CTCCAGCCCTGGGTT | 221178 |
rs73166306 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152469 | CACATTGTGTGTAAC[C/G]ACCTCCTCTTCCGCC | 221178 |
rs73166316 | snp | G/T | 0.47666 | 0.105476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164781 | CCCTGAGGCAGAAAC[G/T]GCACCACAGAACCTT | 221178 |
rs73166318 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165991 | CTCTGGTTCAGAAAT[A/G]TGCTCCACTTCCACC | 221178 |
rs73166335 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183739 | GCTTTATAATGTTCT[C/G]TATGGGCTAATGGTG | 221178 |
rs73166339 | snp | A/G | 0.078151 | 0.181571 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185002 | GGTGCCTTTGAAAGT[A/G]GGCACTGGGGCCGTC | 221178 |
rs73166363 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200658 | CATAACATACGAGAT[A/G]TGAATATAAAGCAAC | 221178 |
rs73166396 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243242 | TGACATATGTTACTA[C/T]GTTACGGCTCTTTTA | 221178 |
rs73168705 | snp | A/G | | | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254407 | TGCTTCAGAGCTTGC[A/G]TCCCATCCAGGGCAG | 221178 |
rs73168712 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259605 | AAAGATTTACTTATT[C/T]ATGTATTTATTTACT | 221178 |
rs73168716 | snp | A/T | 0.209693 | 0.246729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262959 | CGTTCAGGTTATTTT[A/T]AAAAAAAAGAAACTT | 221178 |
rs73168733 | snp | A/G | 0.232359 | 0.249377 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274688 | ATGGGAAGTCAGAAT[A/G]GCTTATCTCAACTCT | 221178 |
rs73168796 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276862 | GAAGGCAGCAGCACC[A/G]GCCTGTGGGTCTGGC | 221178 |
rs73168798 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277051 | TTCAAGTAGAGTGGA[A/G]TCAGATTACAGAGAA | 221178 |
rs73443742 | snp | A/G | 0.151334 | 0.229706 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010776 | GATGGTGTCTTGGCA[A/G]GCAAGGCAGGGCCAG | 221178 |
rs73448972 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138499 | GCGTTGGTTTTATAA[A/C]ATACATTTCTTTAAT | 221178 |
rs73448974 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139263 | CAGTTTCGGGTCCAC[C/T]CTACTCCAGTATGAC | 221178 |
rs73448998 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147891 | TTCATTTAGCGTAAG[A/G]TCCTCAAGGTTCATC | 221178 |
rs73450708 | snp | A/C | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132275 | TGAATGACTTCCCCC[A/C]AAAAATCTTCTGTTA | 221178 |
rs73450904 | snp | C/T | 0.0509478 | 0.151255 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162641 | GTAGCATCTACCAAA[C/T]TCTGGGTGTGTGCCA | 221178 |
rs73450919 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168265 | TCCAGTTTAATTTCT[G/T]TCAGTTTCTAATTTC | 221178 |
rs73450932 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172923 | ACTATGTTAAGTTTC[C/T]GATCAGTTAACACAG | 221178 |
rs73455377 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049645 | TAGGGAGTCTGTAAT[A/G]TACATGCAATGATAC | 221178 |
rs73455715 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273985 | ATGAGCCACTGCGCC[C/T]GGCCAATGGTTAAAC | 221178 |
rs73455722 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280820 | TCCCCCAACCCACCC[C/T]CAAACTCACACACCA | 221178 |
rs73455725 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282678 | CTCTTCCTCCACGTC[A/G]TAGCAAAGTCTGTCA | 221178 |
rs73455737 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287483 | CTTAAGTGCACTCTG[C/T]AACTATCTCTATCAG | 221178 |
rs73455739 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288724 | CACGTGACGACACCA[A/G]TTTTTGAGCTCTGGT | 221178 |
rs73455743 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290367 | CCTTCCAGGATGAGC[A/G]TGAGGCAGGCTAGAA | 221178 |
rs73455745 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294187 | CGTGACTGTGGTGGA[C/T]GGAAAGCACCAGAAA | 221178 |
rs73455751 | snp | A/G | 0.081446 | 0.184634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297151 | TCAGGGGATCCTCCC[A/G]CTTCAGCCTCCTAAG | 221178 |
rs73455753 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298571 | TGAGCACAATCTGTT[A/G]AATGGAAGTCAGGGA | 221178 |
rs73455756 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299869 | TTCACACACTGCACA[C/T]GTACACTGTCACTGT | 221178 |
rs73455758 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299924 | ATGCTCAGGGCACAC[A/G]CTACACACAGCTGGG | 221178 |
rs73455759 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300123 | TATTTGCCCGGGAGC[A/G/T]TCGGGCTTCACACAG | 221178 |
rs73455764 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302229 | GCTCCACACGGAGTA[C/T]CTGAACATAACAAGT | 221178 |
rs73455766 | snp | A/T | 0.0955749 | 0.196603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302529 | GAGTCTCAGCATTTT[A/T]ATTTTTTTCCTTTCT | 221178 |
rs73455777 | snp | A/T | 0.177736 | 0.239986 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305275 | CCTAACAGAGACTTA[A/T]GAATACCAGGATGTG | 221178 |
rs73457149 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058763 | TGATTTATGTTGGGA[A/G]CTATAGATTCACTGG | 221178 |
rs73457811 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190481 | GATTCACCATTCTAG[A/G]TGCCATAAAGAACAG | 221178 |
rs73459039 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104249 | AATGGGTTTTTTTTT[G/T]TTGTTTTTTGGGTTT | 221178 |
rs73459064 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111791 | TTCCTACTTGGTCAT[C/G]ATAGCTATTTTAAAA | 221178 |
rs73461006 | snp | A/C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122626 | CAACTCCTGTAAGAA[A/C/T]CTTTTTGCACATACT | 221178 |
rs73461012 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125864 | CAATTAACTGGAAGA[A/G]TAAGGAAAAGACGAA | 221178 |
rs73461321 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984422 | GAAAGAATTATATGA[A/G]GTTGCTTCTTGGCTC | 221178 |
rs73461334 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987915 | TCTTAAGGCCCAGGT[A/G]TGTTGTGGCATATGT | 221178 |
rs73461353 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994314 | AACATATCTCATGTA[C/G]TATGAATGGAGCTTC | 221178 |
rs73465829 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241026 | TAAAAATGATGTCAC[A/G]ATTACTGACATGCAT | 221178 |
rs73465838 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248697 | GCTCGAGTGTTGGGT[C/T]CTGACAGCCCTGGAC | 221178 |
rs73465841 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250188 | TGAAAAAGACAGTAT[A/T]GTTCATTGTTAAAAT | 221178 |
rs73465846 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252140 | GATCCCTAAAGAACC[A/G]AGACCCAGGCTAGAA | 221178 |
rs73465853 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261538 | GATATGAGTGGGGGT[A/G]AAAATGAGAAGAGGA | 221178 |
rs73465856 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262860 | ATTTAGTCTACTTAG[C/T]AAAGTCCCAGAGCAC | 221178 |
rs73465860 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269093 | AGCGACAGCAGCAGC[A/G]TGACGGCTAACATTT | 221178 |
rs74039539 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985788 | ATAAGAATATAAGAC[C/T]GTGTTGAGGGCAACA | 221178 |
rs74039546 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992941 | ATTCTTCTGTTTACA[A/G]TGCAGCATGGGAATT | 221178 |
rs74039551 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996780 | ACAAGAGGCTGCCAG[C/T]GTTCCTTGGCTTGTG | 221178 |
rs74039560 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000968 | TCCTAGGCTGCTGTA[A/G]CATAGCACCACTGTT | 221178 |
rs74039561 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001491 | GTTAAGGAGTGGCGG[G/T]GGAGAGGGGAGAATG | 221178 |
rs74039564 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008667 | ACACTGGAGGAGGCA[C/G]CAGGCCTGGGCCAGC | 221178 |
rs74040214 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121681 | TTTGAGTTTTATACT[A/G]CAAATGAGACATTTT | 221178 |
rs74040216 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122455 | TCGTCTCCATCTTCA[C/T]CAGCCTGCTTAGCCA | 221178 |
rs74040217 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122563 | CTTTGCACTGCAGAG[C/T]GATGACCTCTAACAA | 221178 |
rs74040218 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122738 | ATCTGTAAAGTAATC[A/G]AAGCCATCTTGCTGG | 221178 |
rs74040220 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123599 | TTTCCTCTTACTACA[G/T]GCTGTAAACAAAAGT | 221178 |
rs74040222 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124410 | GAGGTGTAGAGCCCC[C/G]TCAGTGTCTAACATA | 221178 |
rs74040433 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212970 | TTTAGAGGAGCTGAC[C/T]TTGGAGCGGGTCTGA | 221178 |
rs74040445 | snp | C/T | 0.117188 | 0.211804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242137 | AATATGAATTTACTC[C/T]ATGAAACAAAATCGA | 221178 |
rs74040446 | snp | A/G | 0.158632 | 0.232706 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242138 | ATATGAATTTACTCC[A/G]TGAAACAAAATCGAC | 221178 |
rs74040447 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247174 | TGCTATTCTGGGTGC[C/T]GTCAGTGGAGAGAGA | 221178 |
rs74040450 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251244 | GCTCATCTATGCCAG[A/G]CTCTGTGTCGGTGGG | 221178 |
rs74040452 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253301 | CCAAAGAGTGTTATT[C/T]TAATGACACTCTAAT | 221178 |
rs74040453 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264230 | TAAAAAGTAAAAGTT[A/G]TTGAAAATATCGTCT | 221178 |
rs74040456 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271013 | TCTCTCTCTCTCCAC[A/T]CTCTCTCACTCTCTC | 221178 |
rs74040653 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283241 | ATTATATTTCCACTT[C/G]CTGGCTGCAGTCATC | 221178 |
rs74040654 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284935 | ATTACTGGCTGGCGA[A/G]TGGCAGAGCTGGAGG | 221178 |
rs74040655 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290276 | CAAAGAATAAGCAAC[A/G]ATTAAAACTGCATAC | 221178 |
rs74040656 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293251 | AAAAAACAGGGAAGT[A/C]AAGAGAGCCACAAAA | 221178 |
rs74040665 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299403 | AAACTGGATGCATTC[C/T]TTGCCTCGAATATTT | 221178 |
rs74040667 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300933 | AAGATGTAAAGGTTC[A/G]GTACATCAGGCAAGG | 221178 |
rs74040669 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302967 | GTGGAAGGGAGGAGA[C/T]GGTCATGACACAAAG | 221178 |
rs74040670 | snp | C/G | 0.0944967 | 0.195752 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307458 | TCACTCGCCCTTTGC[C/G]GGTGGGTAGATTAGA | 221178 |
rs74040672 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307531 | ATTGTTTGCTGTGGC[G/T]GTAATCAGAAAAGGA | 221178 |
rs74041904 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170877 | TAGGTTTATATGATT[C/G]GTTGTTGGGAACAGA | 221178 |
rs74041908 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175499 | AGAAAACCCAGCTTG[A/G]TCTCAGAATCAGAGT | 221178 |
rs74041909 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176381 | TGGAAGGGCAGCAAA[G/T]ACCTTGGTCTATTAC | 221178 |
rs74041914 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178295 | CTGTGAGCATGCTCT[C/T]GAAAAATACTTGTGG | 221178 |
rs74041931 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198783 | CTAGTAAAGTTTCTG[C/T]AGGTCAGCAAAGTTA | 221178 |
rs74041932 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199391 | AAACAATCTCATTCT[A/G]CATACTGATTCTACC | 221178 |
rs74042409 | snp | A/G | 0.107694 | 0.205546 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100247 | TTACTGAACCTTTTT[A/G]CCAAGTGGCACCTAT | 221178 |
rs74042416 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104252 | GGGTTTTTTTTTTTT[G/T]TTTTTTGGGTTTTTT | 221178 |
rs74042437 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118603 | CTGACCCAGTGGGTC[C/T]GGGGTAGGGTCTGAG | 221178 |
rs74042709 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140619 | TGCTCTTGTGCGTGT[C/T]CTTCTGAGACAGCTC | 221178 |
rs74042710 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144005 | GCCCAGGGTTGGCCA[G/T]AAACACTCAAAGCAC | 221178 |
rs74042711 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144948 | TTTGGATGAATATTT[C/G]ATTAGACCTATGATC | 221178 |
rs74042712 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146000 | GCAGCTGAATGTGGT[A/G]AGGAGTGGCAGACAC | 221178 |
rs74240452 | snp | A/G | 0.341909 | 0.232492 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029202 | AGCTGGAACTTACAG[A/G]CATGTGCCAACACAG | 221178 |
rs74240454 | snp | A/G | 0.339429 | 0.233457 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029418 | ATGTTAGGGCTGGCT[A/G]ATAGCCACAGATTCT | 221178 |
rs74240464 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233831 | GCAAGCCAAAGCTGC[A/G]GAATCCCGAGTCTCC | 221178 |
rs74322995 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157900 | TCGTTCAACCCTTCT[A/C]ACTTCATTTGCCCCA | 221178 |
rs74333469 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030909 | AATTTTACAGAGAAC[A/C]CTGAGATTTTAAAAG | 221178 |
rs74343319 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284905 | TTTCATCAACGCTCT[A/G]AGGAAAGATGTCTAA | 221178 |
rs74345127 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005871 | AGCTGACATTTTTTT[C/T]CCTTCTTAATAAAGA | 221178 |
rs74381603 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150564 | TGATTTTTTTTTTTA[A/G]GGAATTGCACACAAA | 221178 |
rs74382575 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075017 | TGCAGTTTGGTTATG[G/T]TTTCCTCTGTATGGA | 221178 |
rs74402885 | in-del | -/CAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077262 | AGCGAGACTCCATGT[-/CAAA]AAAAAAAAAAAAAAA | 221178 |
rs74404773 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031648 | ATACATTGAGCTTAT[A/G]TCAGGCACTGTAGAT | 221178 |
rs74416711 | snp | C/G | 0.0134861 | 0.0810011 | downstream-variant-500B, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307123 | GGAGGAAGTGGAGAG[C/G]TGGGTGCGGGGGCTT | 221178 |
rs74426513 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156381 | TGGGGGCCCTGTCTC[C/T]GAGCAGACAGGGAGG | 221178 |
rs74437287 | snp | G/T | 0.0125392 | 0.0781817 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224805 | ATGTACGAGATTCAT[G/T]GAGATGACATTTGCC | 221178 |
rs74479286 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106578 | CACCAGCCACATGTA[C/T]AGAACAGCACTCGCT | 221178 |
rs74484757 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228281 | ACCATGCCCGGCTCA[G/T]GTTTTCTATTTTTTT | 221178 |
rs74489960 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277445 | CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 221178 |
rs74498138 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202869 | TACGGAAGCATTCCA[C/T]TTACTTGCCCAATTT | 221178 |
rs74499696 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150736 | TTGCAGTCTTGAGGC[C/T]GAAGTCCTTCTTCCT | 221178 |
rs74499784 | snp | A/G | 0.107694 | 0.205546 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185272 | TGATAGGCACTCAGT[A/G]AAGTTTTACTGCTTG | 221178 |
rs74509055 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222729 | GCTTTCATCTGACCA[G/T]CCCTGTGCTGGAGCG | 221178 |
rs74546053 | in-del | -/G | 0.0437281 | 0.141251 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033611 | AGGTTGTGGATCCTT[-/G]GCCCAGCCTGCAGTG | 221178 |
rs74556397 | in-del | -/TGGTGGTGGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044904 | GGTGGGGGTGGGGGT[-/TGGTGGTGGG]AGGCAGAGTGAAGAG | 221178 |
rs74556707 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193700 | CCCTTCGATTTGGCA[C/T]TTAGCTATGCTTTAG | 221178 |
rs74574637 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180299 | TTGAAAATGAATTGA[C/G]CATGACTATAAAATT | 221178 |
rs74613348 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211186 | TTTTCTGTATATTAG[A/T]TAACATCATTTTCAA | 221178 |
rs74625215 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242785 | TAAATATTTCCTTGT[G/T]CCTGCTTTCAACTCC | 221178 |
rs74625276 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979311 | TGTGTGTGTGTGTCC[C/T]TGCTGCCTGAGGGTG | 221178 |
rs74627047 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006571 | GGCCAGGCCGGCCCA[A/T]GTACTAATTCATCAC | 221178 |
rs74628437 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996135 | TAACAAGTTCCCAGG[A/G]ACCTAATGGGATTAT | 221178 |
rs74636852 | snp | A/G | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255097 | CCTAACCAGGAGTGC[A/G]CACGAGCTAAATCCT | 221178 |
rs74648142 | snp | C/T | 0.250732 | 0.249999 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987892 | GCTTATTTCACATAA[C/T]GCAACGTTCTTAAGG | 221178 |
rs74663373 | snp | A/G | 0.316243 | 0.241064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210452 | TTGATTTTTGGAGTA[A/G]GAGGCCAATTTTATT | 221178 |
rs74665457 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264300 | GAAGAAAGAATATTA[A/G]AAGTCAGAGGAAGGA | 221178 |
rs74667933 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982850 | GCAAACCAGGTACAC[A/G]TGTGAGCTTCGGGAG | 221178 |
rs74681838 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287442 | TGCTGGGATTAGAGG[C/T]GTGAGCCAGTGTGCC | 221178 |
rs74693895 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013428 | ATGGGCAGCCCCCTC[A/C]CCCTTGTGCCTTGCC | 221178 |
rs74694668 | in-del | -/TA | 0.343701 | 0.231776 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034510 | TGTCTTCCCAAATTC[-/TA]TATATATATAACAGA | 221178 |
rs74701715 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003850 | TACAATATTAGAGAC[A/G]TGGGAAAAAACACAA | 221178 |
rs74705040 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203324 | CCTGACGGTAATTTA[A/G]GGGAAGGGGAAGAAG | 221178 |
rs74706104 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052591 | ACCCTCCCGTTTCCA[A/G]ATGAAAGCCAGGCTG | 221178 |
rs74707307 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146406 | GAGTACCCTTGTGAT[C/T]GTTAGCTGCTTCCAT | 221178 |
rs74717288 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288233 | GCACAGAGAAGTTAA[A/G]TGGTGGGATTGGATT | 221178 |
rs74735820 | snp | A/T | 0.114036 | 0.209795 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019096 | ATTATTATTATTATT[A/T]TTTTTTTTTTGAGAC | 221178 |
rs74741961 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114391 | CACATGCGCGTGTGT[C/G]TGCATGTGTGCACAC | 221178 |
rs74757252 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186686 | GCATAACATTGTTAC[A/G]GGAACATTAATTTTC | 221178 |
rs74764856 | snp | A/C/G | 0.00597534 | 0.0543715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021521 | TAAAAATTAAAAACC[A/C/G]GTATCAGGCTGAAAA | 221178 |
rs74765051 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071004 | TATGTATATGTCTAC[A/G]TCTGTGTTAATGTCT | 221178 |
rs74794215 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069838 | CCAAATGGCACTGAC[C/T]GTTGTGACAGTGAGA | 221178 |
rs74808553 | snp | A/G/T | 0.011925 | 0.0764466 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040730 | TTGAAAGGGGGAAAA[A/G/T]GGTCGCTTCAAGGCA | 221178 |
rs74810273 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233611 | TTAACAATGGAATCA[G/T]TTTCTAAGTCAGTTT | 221178 |
rs74825246 | snp | A/G | 0.104859 | 0.203554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217808 | GGAGCTTCCCAGCAG[A/G]GCTGGAGCCACAGAG | 221178 |
rs74828967 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216654 | TTCTTTTACTAAGGT[A/G]TGTATATTGGGGCTA | 221178 |
rs74844538 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002137 | ATGGGCTTCAAAAAA[A/G]CAGTGTCATAGCTTT | 221178 |
rs74853852 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066284 | TTCCAGATATGCCCC[A/G]CCTGAATTTCACACA | 221178 |
rs74855815 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294145 | GCTTGGGAGCGGGGC[A/C]CTCCTGGGGAGAACA | 221178 |
rs74860642 | snp | A/G | 0.0169479 | 0.0904805 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135225 | CATTATTCGAAAAAA[A/G]AAATACTTTTTCTTC | 221178 |
rs74864278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051218 | GCACATACCTTGTTG[C/T]AGTGGCCACCTGACC | 221178 |
rs74877607 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275605 | ATTTCAATTTGGAGC[A/G]GTCTTTGCTTCTTGT | 221178 |
rs74888778 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285054 | CCTCCAGCTTTTGGC[A/G]TTCTTGAGCAGAACG | 221178 |
rs74922738 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218791 | AAGACAATTCTTTCA[A/G]TGTGACCCAGGAAAG | 221178 |
rs74925224 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983658 | TTGTTTTTTTTTTTT[A/T]AAAAACATCCAGAAC | 221178 |
rs74934639 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230665 | GCTGAGGTGATGTGT[A/G]GACTTAACATGGGGC | 221178 |
rs74956097 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135058 | AAAAGACAGGGATAG[A/T]TTCTCCCTCATAGCC | 221178 |
rs74966772 | snp | G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237694 | TGGAGGTGGGTGCAG[G/T]GGCACATACCTGTAA | 221178 |
rs74977622 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084036 | TCTGAAAGTGGAAGG[A/T]TTTCTGGATTATAGT | 221178 |
rs74982400 | snp | A/G | 0.350764 | 0.228794 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073024 | GTAGATCTTGTCTCT[A/G]TGAATTTATAGATTT | 221178 |
rs74984052 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232548 | TTAAATTTTTTAATA[A/T]TTTTCTTTTTTGAGA | 221178 |
rs74987271 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997346 | CCCCTGTGATCCGAC[C/T]GTCCCCATACCCACA | 221178 |
rs74998801 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222744 | GCCCTGTGCTGGAGC[G/T]TGCCTCTTCTTCTGT | 221178 |
rs75032010 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128936 | AAGATCAAGTAATGA[C/T]TGGTTCCACTAAAGG | 221178 |
rs75047645 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296807 | TTTCTAGTAAGCAGG[A/G]AAAAAAAAAGAAAAG | 221178 |
rs75068830 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074647 | AGTGATTAAAAAAAA[-/AA]CCCTTGTAGGAATTA | 221178 |
rs75081163 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097469 | GTGGGTGATGACCAC[C/T]TTTTCCTAGCTCAAA | 221178 |
rs75084673 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053583 | TGCCACCTGGGCCCA[C/T]GGTGGGAGTATTTTT | 221178 |
rs75116624 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983645 | TATATTCTGTTGGTT[G/T]TTTTTTTTTTTTAAA | 221178 |
rs75121135 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253237 | TAAGTATTTAACAGA[A/G]CAGACAGTACTATAA | 221178 |
rs75124222 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205067 | CACTACTCCTATTCA[A/G]CATAGTATTGGAAGT | 221178 |
rs75143929 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285312 | TAAAGTATGAATGAT[C/G]CACACTGGAGGGAGA | 221178 |
rs75189966 | snp | C/T | 0.105569 | 0.204058 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077700 | CAGTGTATTATAGAG[C/T]GGCACACACTATGCT | 221178 |
rs75191070 | snp | A/T | 0.00272338 | 0.0368005 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223355 | AGAGGCTTCGGAGCA[A/T]GGCCTGGGAAAGTCC | 221178 |
rs75198785 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193932 | ACATTGTGATGAGTT[C/T]AGAAGGGTGGAAGCT | 221178 |
rs75207076 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211305 | GTTGAATGGAAGTGG[A/T]GAGAGTGGACATCCT | 221178 |
rs75222553 | in-del | -/T | 0.364401 | 0.222289 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173512 | CCCCCGTCCCCCAAC[-/T]TTTTTTTTTTTTTGG | 221178 |
rs75230854 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204540 | CTATTACTACCATTC[A/G]TCTCGAGAACTGTTC | 221178 |
rs75235178 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075467 | ATCTTTTCATTAAGC[C/T]AAGGGTTTAAATAAA | 221178 |
rs75252439 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071642 | TGTCTGACCGTACAT[A/G]CAAACAGGCACACCC | 221178 |
rs75253852 | snp | C/T | 0.000282313 | 0.0118776 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224349 | CCCAAGCCCCAGAGC[C/T]CTCAGAGCCCCCAGA | 221178 |
rs75286780 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028723 | GAATGTTTGTCCGTT[A/C]TTACGCTTCAAGCTT | 221178 |
rs75293542 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171104 | AATTTTAGTTGGAAA[C/T]ACATTTTCCCATTCG | 221178 |
rs75295615 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118281 | CAACAGGGGTCTAAT[A/C]CCTAATTTATAGATA | 221178 |
rs75298853 | snp | C/T | 0.0584853 | 0.160693 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255432 | CTTTGTGGAATCACT[C/T]ATCTGTTTTGTTCCT | 221178 |
rs75302294 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070743 | AAGGCCTCAATAGAA[C/T]GGAAGGCTGACCCTC | 221178 |
rs75320661 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117685 | AAGAGAAATTAAGAG[A/G]AAAAAAACCCCAAAC | 221178 |
rs75320930 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025218 | AAAATTTTTATTAAA[A/C]TGAATCAAATTTGTA | 221178 |
rs75323163 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281832 | GGCTGGGAGAGGCGC[C/T]GCTGGCAGCACGTGC | 221178 |
rs75353251 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057545 | GTCTTATGACCAAAG[A/G]CACTGAAAGGACTGG | 221178 |
rs75353853 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010068 | TACATGTAAGATGTA[C/T]ACTGGTTTTGTCCTG | 221178 |
rs75359487 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097330 | AATAATTTCCCCAAG[A/G]TCATGCAACTAGTAG | 221178 |
rs75374660 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044233 | TGTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs75388507 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130015 | AGTGCAAAGAGGTGG[A/G]TGAGGTAGCCAGGAG | 221178 |
rs75391465 | snp | A/G | 0.124837 | 0.216412 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091434 | CAATTGCCATTAATA[A/G]TGTTTGACAAATGCC | 221178 |
rs75425158 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045897 | AGCCTCATTTCCCTA[A/T]TCTGGAGAATGGGAT | 221178 |
rs75427232 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075037 | CTCTGTATGGAAAAA[A/C]CCTTAGGCCAAGGTT | 221178 |
rs75439322 | snp | A/G | 0.0733688 | 0.176922 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254712 | CTGTCTGGTTCCTGC[A/G]GGGAACCGTATCATC | 221178 |
rs75447098 | in-del | -/TTTA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983655 | TGGTTGTTTTTTTTT[-/TTTA]AAAAACATCCAGAAC | 221178 |
rs75449334 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154450 | TGCATGACTCCATTT[A/G]TATGAAGTTCAAAAA | 221178 |
rs75452924 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205068 | AACTTCCAACACTGT[A/G]TTGATTAGGAGTGGT | 221178 |
rs75455320 | snp | G/T | 0.030278 | 0.119257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171180 | ACTGCTCACTAGAGC[G/T]GGGTGGTTTTAGATC | 221178 |
rs75455683 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220240 | TATGACAGCACCAAG[G/T]TTAGGCCGATTCCCA | 221178 |
rs75456123 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226856 | CTAGAAAGTAGGACT[A/G]TCGCAGAGTACTTTC | 221178 |
rs75499437 | snp | G/T | 0.375 | 0.216506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029708 | GTTTGTTGTACAGAT[G/T]ATTTCATCATCCAGG | 221178 |
rs75509495 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267052 | TCACTAAAAAAAAAA[A/T]TTAAGCTGAAAGTCC | 221178 |
rs75525874 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108024 | GAGTCTGGGAGACCA[A/G]GATCAGGGCACTGGT | 221178 |
rs75531285 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029817 | TGTGTGTTTTTCTCC[C/T]CTATGTGTCAGTGTG | 221178 |
rs75550181 | snp | C/T | 0.0376037 | 0.131863 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979589 | AAGAACAGCAAACAA[C/T]AGCACAGCCCCGGCC | 221178 |
rs75550958 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092463 | TTTATATTTTAGAAG[C/G]AGAAGAGTTAATAGG | 221178 |
rs75557883 | snp | C/T | 0.139225 | 0.224118 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148935 | GTTTATACCAGGAAA[C/T]GCTCTCCTATGCATG | 221178 |
rs75559564 | snp | A/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222189 | AAAGACCCCCACCAA[A/T]GTGTTTCCTTCTCAG | 221178 |
rs75564365 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271972 | AAATTTAGAAAAAGG[A/G]AAAAAAAAGTTGCCT | 221178 |
rs75572770 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097970 | GAATACTACATGAAA[A/G]CAGAAGGACCTCCAT | 221178 |
rs75589766 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281242 | GGGAATTTACTCCTC[C/T]CCCTCCAACCCCGTC | 221178 |
rs75592266 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171427 | ATCACACGTGTCTCA[C/T]GTATGGTTTCCTGTT | 221178 |
rs75611445 | snp | C/T | 0.117537 | 0.212022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187810 | TCTTCTCAGGCCTTC[C/T]TATTTCCTGAGACAG | 221178 |
rs75618126 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157721 | CTGCCCTGTACCTCT[G/T]GAGAAACCCCTGCTG | 221178 |
rs75623268 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117300 | CTGATGTTAATTTTA[C/G]GAATTAGCCGTCACT | 221178 |
rs75624457 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283349 | TCATTCCGTTGGAAA[A/C]AATACTGATAGATTG | 221178 |
rs75631717 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033522 | TTTCAGCTCGGACTG[A/G]CCTGGAAGAAGACCC | 221178 |
rs75649545 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197669 | GGTCAAAATAAAGTA[C/T]GTCCTAGAGAATGAA | 221178 |
rs75667787 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125304 | GAGCCCCTTGACTTA[C/G]AGTAGGGAAACTTCC | 221178 |
rs75671627 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038581 | CTTCGGTAAAGTGCC[A/G]AGAGTAAGGATTTTA | 221178 |
rs75672682 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060359 | TATTCAATAAATGGT[A/G]CTGGGATAACTAGCT | 221178 |
rs75702786 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056455 | CAAGACATATGATGG[A/G]TTAGATGCTCACCTT | 221178 |
rs75705817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016111 | CAAGTCCCTGGCAGG[A/G]CTCGGGACTCTGCGT | 221178 |
rs75716177 | in-del | -/TT | 0.177182 | 0.23916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204377 | TTAACTGGTAAATTG[-/TT]TTAAAAGCATTGTTT | 221178 |
rs75728856 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071078 | CATGATGAATGCACT[C/T]ATGGTTCAGGGAGGA | 221178 |
rs75740540 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242919 | TTTTGGTTATGACAC[A/T]TTAATTTTCATTTAA | 221178 |
rs75743154 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063802 | TCCAGCTTTCTTCTC[G/T]TAGTCGCTGTCCTGA | 221178 |
rs75745974 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257233 | TAGCTTGCTTTTCTT[A/G]TCTTCCAGAGAGGAG | 221178 |
rs75755612 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246213 | TTCTGTTTTTCTAGC[A/G]TGTTGTTCCTGAACC | 221178 |
rs75757659 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005036 | TTTTTCATGACATAT[A/G]GGTTATCTTTGCCAC | 221178 |
rs75757908 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212748 | TTGCCAGATATTGAA[A/G]AAAAGAAAGGCTGGC | 221178 |
rs75757953 | snp | C/T | 0.148326 | 0.228391 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006894 | GCTCGGCAATTAACA[C/T]GAAGCCCCTCTCTGG | 221178 |
rs75759104 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114239 | ACAAAAGAACAATTG[A/T]TATTCCTCTTTGTGG | 221178 |
rs75782961 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005799 | GGCTCAGCAAGATGC[A/G]GCATGGGCATTTTTG | 221178 |
rs75787993 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064783 | AGGTCAATACCACCA[C/G]TGATGTCATGAGCAT | 221178 |
rs75793460 | snp | A/C/T | 0.0600789 | 0.162992 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279865 | CTGGCCTCTGCCCCC[A/C/T]ATCTCCTGGCCAGGA | 221178 |
rs75794370 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135716 | AAAAAAAAAAAAAAA[A/G]AAGAGTATTTTTAGA | 221178 |
rs75798263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099514 | CATTTTCTTGACCAT[A/G]GAAAGTTCTGTCAGA | 221178 |
rs75806787 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001767 | GGTTGAAGAAGTAAA[A/G]AGAGTCAGCACTGGG | 221178 |
rs75807955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016114 | GTCCCTGGCAGGACT[C/T]GGGACTCTGCGTATG | 221178 |
rs75819530 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066384 | GGAAACTGAGACTCA[A/G]AGTTTAAAGGATTTG | 221178 |
rs75836977 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046706 | TAGAAATTTGGGTTT[C/T]CTGTTTGAGGACTTT | 221178 |
rs75859902 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051122 | GAATGTCACTGAGCA[A/C]ATGAACTCCAAGTGA | 221178 |
rs75864386 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108163 | GGGACACGCCCCTCA[A/G]GCCCTTTTATAGGGT | 221178 |
rs75880505 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029220 | TGTGCCAACACAGCC[A/G]GCCTCTGAAAATCTT | 221178 |
rs75891877 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217201 | AATTTGAGGCCACCC[C/T]GGGCAACATAGCAAG | 221178 |
rs75892078 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984500 | TTTCTATCATGGCCC[C/T]GCGCAGCACCTGTCC | 221178 |
rs75892266 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280240 | TTCCAGTCCGTGTCT[C/G]TGTCCAGAGGTTTTT | 221178 |
rs75893557 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071175 | TTGAATGATGAGATA[C/T]GATTCCTTTGTAGAG | 221178 |
rs75899372 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150092 | GAGGAGACGGAGCTG[A/G]GCAATGCTGAGATTC | 221178 |
rs75910905 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985279 | GCATGAAATGTGTCA[C/T]GACCTTTCTTCCTGA | 221178 |
rs75911939 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034573 | ATAGTTTAAGGCAAC[C/T]GTTTTATTATTCCCC | 221178 |
rs75922381 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067128 | CATGCTGCCCCACAC[A/C]CCACCAAGCTGCATA | 221178 |
rs75957959 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083871 | GGGGGAAAAAACCCC[A/C]GTCTGGAGATGCAGG | 221178 |
rs75961756 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092947 | CTTCTCATTAACGTT[A/G]CAGATGACTATTTTC | 221178 |
rs75972978 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029755 | GGAGGGAGAGGATCA[C/G]GAAAAATAACTAATG | 221178 |
rs75976076 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228115 | CTTGTACTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs75989747 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289946 | AGATTTTAAGTGGCT[A/G]GGCATAATGTTTTTG | 221178 |
rs75990437 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251569 | TGAGTTGCCACTGGG[C/T]TTCGGTGCAGCCTGC | 221178 |
rs76008309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040034 | TTGGCCAATCACAAG[C/T]ACCGTTTGGTGAGGT | 221178 |
rs76014198 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119773 | TAGCTGCCAAGGAAG[A/G]AAGCCTGGGAGAGCT | 221178 |
rs76020214 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244768 | CCTGGGAAGCTGACA[C/T]GGGAGGATCACCTGA | 221178 |
rs76024945 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122884 | AAACAGTAGGAACGA[A/C]CTGTAAGCAGATTCC | 221178 |
rs76025995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072535 | TGAGCCTCCTGACAC[A/G]GTTGTTTAGACTCAC | 221178 |
rs76040624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034883 | CACCACTCTGCCATC[A/C]TCTATGGCTTAAGCA | 221178 |
rs76045968 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047827 | GATCATGGAGGCTGA[G/T]AAGCACAGGATCTGC | 221178 |
rs76051548 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155418 | TTCAGGAGTTACTCA[A/G]TTAAATCAAAGAGAA | 221178 |
rs76086924 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141502 | CCTTCCTTGACTCCT[C/G]CAGCTGAGCTCTAAT | 221178 |
rs76098500 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214599 | CTGACCCCAAATTCT[G/T]AGCCTCAGCTGCTGC | 221178 |
rs76156318 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171301 | AAGAGACGAAGGAAG[A/G]TGGTGAAGTCGTGAC | 221178 |
rs76164706 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068146 | TTACTTTGCCTGATC[C/T]TCTTTGCCTCTCACC | 221178 |
rs76169932 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292297 | CATCACAGCACAGCC[C/G]AGCTGTTGGGTACCT | 221178 |
rs76179269 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24028726 | TGTTTGTCCGTTCTT[A/T]CGCTTCAAGCTTTTA | 221178 |
rs76184365 | snp | C/G | 0 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978118 | TCGGGAGCTTGAGAC[C/G]AGCCTAACCAACATG | 221178 |
rs76220971 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178324 | GGAATTAGCAGAAAT[C/G]TATTGAACTGCATTA | 221178 |
rs76233018 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150947 | ACTGGGCGCCATGGC[C/T]CAGCCAAATTGATGC | 221178 |
rs76243153 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195828 | TATTAACACCTGTTA[A/C]CAAGTTGACTAGAAA | 221178 |
rs76243900 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208069 | AAAGAGCTTTCGGCA[C/G]GGAAGGGACGAGCCT | 221178 |
rs76249356 | snp | C/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218649 | GCTGCATGTGGCCCA[C/G]GGAAGCTTTGAATGT | 221178 |
rs76286419 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263588 | TATACTTTAAATCAC[C/T]TCTAGATTACTTAAA | 221178 |
rs76291332 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296189 | GGCCTTATAGACTTC[C/T]GGAGTTTGGGCAGGA | 221178 |
rs76318976 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234563 | ATTAGAAGGAATGCC[G/T]TACGTTTTGTTGGTG | 221178 |
rs76320389 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182705 | AGAGGACAAACATCT[A/G]GACCATATCAATGGC | 221178 |
rs76320861 | snp | A/C | 0.117188 | 0.211804 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187771 | TTGACTGCTTCACTG[A/C]TGGCCACTCCCAGTC | 221178 |
rs76324689 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303486 | AGAATCCACTGCTTT[C/T]CAGGCAAGGAGGGAG | 221178 |
rs76342710 | snp | A/T | 0.134802 | 0.221877 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246537 | GCGTTTGTGCGTGTC[A/T]CTGTGTGTGAGAGAC | 221178 |
rs76346583 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271980 | AAAAAGGAAAAAAAA[A/G]GTTGCCTGGCGATTT | 221178 |
rs76364690 | in-del | -/CCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015815 | GAGCCTCGGCTGGTG[-/CCA]ACACGTCATAGTCCC | 221178 |
rs76371117 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234026 | TAGAATAGTTTCTCT[A/G]GTGAGATACCATTAA | 221178 |
rs76388747 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217715 | GCTACCAGCCCCTGG[A/G]CTGGAGTGGTAAACA | 221178 |
rs76407234 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024576 | CCACACAGCACGGTT[C/T]TACAGAGCAGCTGGC | 221178 |
rs76413773 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24263892 | GTCTTCTGACTGCTG[C/T]GAGACAGCCTGGATT | 221178 |
rs76417027 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013383 | CTTGCTGCTCAGTTT[C/T]CCTCCTGGTTTGTCC | 221178 |
rs76441075 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038362 | AGTTCCCTCTGTTCT[A/C]TGTTTACATTGGAGT | 221178 |
rs76445460 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305235 | TGAGCCCTAACTTCC[A/G]GCTCCCACCTACCTC | 221178 |
rs76448622 | snp | A/G | 0.0637235 | 0.166737 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255448 | ATCTGTTTTGTTCCT[A/G]GGGACCCCGAGATCA | 221178 |
rs76457539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094429 | GAAAACTGTCCCATC[A/G]CAAGATATCTCAGAA | 221178 |
rs76457543 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058101 | TGATCCCACATTGGA[A/G]TGTTATGTCTTTGTA | 221178 |
rs76466510 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003138 | CAATGGTTCTGTCTG[C/T]AGCATTTTCCCCACG | 221178 |
rs76483291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241457 | AACGCAGAGTGTTTT[A/G]CCATTTACTTAGTTT | 221178 |
rs76500370 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290332 | TTGTGGGAGGGGGAC[A/G]TTAGAGGCCCTGCTC | 221178 |
rs76504580 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062293 | CGGAGCACAATGCAA[A/G]ATCCTGTGGATATGG | 221178 |
rs76510234 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176985 | GGTCAGGCTGATCTC[A/G]AACTCCTGACCTCAG | 221178 |
rs76512181 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140335 | ATGCTCAGGAAATCA[C/G]TTCATAGTTTGTTGC | 221178 |
rs76513994 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070787 | AGAATTCCCCCTCCC[C/T]GACTGTCTTCAAACT | 221178 |
rs76521322 | snp | A/C | 0.240478 | 0.249819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218776 | TTTTATGTGTGGCCC[A/C]AGACAATTCTTTCAA | 221178 |
rs76521621 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985151 | TGGGCATAGTGAAAT[A/G]CCCTTTCTTCCCGTC | 221178 |
rs76530849 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285699 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTTTTGCT | 221178 |
rs76545894 | snp | C/T | 0.095934 | 0.196885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047582 | CAAATTTTGCAAAGG[C/T]AGTTTCATCAGCTTT | 221178 |
rs76548847 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23982177 | TTTTAAATTTTTTGT[A/C]AGATTTCTTACTTTC | 221178 |
rs76574536 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021729 | ATCTTTTTTTTTTTT[G/T]GAGATGGAGTCTCAC | 221178 |
rs76576322 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216244 | CACCAGCCTGACCTG[A/C]AACTTTAGACACAGA | 221178 |
rs76582397 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020349 | CAAAAATATAGTGCT[A/G]TGTACATGTGACTTT | 221178 |
rs76595688 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083409 | ACAAACAAGTCAGCA[C/G]AGTCAAGGAGGGCAG | 221178 |
rs76601905 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114081 | TTAGTGCTTATCTAA[A/G]AGGTGCAAGACATTC | 221178 |
rs76610780 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209367 | ACTAGATTGCTGCAC[G/T]TAAAAGTATGGGGTA | 221178 |
rs76616048 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124856 | GATCAGATGTTACTA[A/G]CATATTGTCAGATTT | 221178 |
rs76619708 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020871 | AGATGGTGAAAACCG[C/G]TCTCTACTAAAAATA | 221178 |
rs76642735 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237785 | GCCTGGGCAACATAA[A/C]CAGACCCCATCTTAT | 221178 |
rs76650125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178530 | GTAGTAGTAATAAGT[A/G]CCCTAATAAATGAGC | 221178 |
rs76684555 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048724 | GACCCAAGCTGAACC[A/G]TTTAATATCAGAGTG | 221178 |
rs76707536 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280573 | GTGCCAGATCAGTGG[C/T]TGCTAAAATTGGAAG | 221178 |
rs76708644 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094301 | TTAACATAGAAAAAC[C/G]AGGTTTTGACTGCAG | 221178 |
rs76714905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078332 | AATGGGCATGATAGT[A/G]GTTTTGATATTTTTG | 221178 |
rs76717202 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016358 | ATTTCCATTTGGATC[C/T]AGATGTGACATCTTC | 221178 |
rs76721076 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145726 | TGGAGAGAATTGTGC[A/C]TGATCAATAAATAGA | 221178 |
rs76722656 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993529 | TTTCACAGATGTCAA[A/T]TGCTTGATGCCAGTT | 221178 |
rs76754730 | in-del | -/CATATATATATAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024933 | AAAAACATTCAAATT[-/CATATATATATAA]ATATATATATAAATA | 221178 |
rs76757138 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205053 | ATTGAATAGGAGTGG[C/T]GAGAGAGGGCATCCT | 221178 |
rs76765245 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146396 | CCAGATCACCGAGTA[C/T]CCTTGTGATCGTTAG | 221178 |
rs76768482 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977647 | GTCCAGCCTGGGCAA[A/G]AAAGTGAGACACTGT | 221178 |
rs76768641 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205102 | GCCAGGGCAATCAGG[A/C]AAGAGAAAGAAATAA | 221178 |
rs76776566 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184275 | TGGGAAAAATGTTTG[A/G]TTTTGCCCTGAACCC | 221178 |
rs76797322 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204226 | TTTAATTCTCACTGC[C/T]GTCCTCCAGAGTCTC | 221178 |
rs76816055 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135189 | TACTTTGTTAAGGCA[A/C]CCCTAACAAATGAAT | 221178 |
rs76821797 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021728 | AATCTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA | 221178 |
rs76825047 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135226 | ATTATTCGAAAAAAA[A/G]AATACTTTTTCTTCT | 221178 |
rs76842799 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107696 | CATTTTCAGTTTTTA[G/T]TGAAACTATAGACTT | 221178 |
rs76869103 | snp | C/G | 0.289165 | 0.246913 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110960 | AGTCTTGCTCTTGAC[C/G]AGGCTGGACTTCAGT | 221178 |
rs76901072 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23981007 | CAGATTTGGATCCAC[A/G]AAACGAATTGTTCCT | 221178 |
rs76901609 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302206 | TTCAGTGAGAGAGAC[G/T]GTGTCACGCTCCACA | 221178 |
rs76902741 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029122 | AGTAACGGGGTCTCA[C/G]TGTGTTGTCCAAGCT | 221178 |
rs76911795 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981767 | CAAAAGCCACTGCTA[C/T]GACATATATTTTGGA | 221178 |
rs76919832 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029816 | ACATCAACACATAGA[A/G]GGGAACAACACACAC | 221178 |
rs76923872 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246120 | CCCCAAAAAACTAAC[A/T]AAAAATAGAACAGAA | 221178 |
rs76928167 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228613 | AGGAAAAGGGTGACA[C/T]GCAAGGATTCCAGCC | 221178 |
rs76935329 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136081 | ATGAAGCTCAGTTGG[A/G]CTGGTGTGGGAGAGA | 221178 |
rs76938661 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993039 | TTATGTGCCTGGGCT[A/C/T]GGTCCAGGCTGCTGT | 221178 |
rs76941022 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033441 | TAATGACTATGGGAA[G/T]GCTGGCTGTGCAGAG | 221178 |
rs76942041 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084400 | GGCAGGATGCCCGGG[A/G]AAGAAATCTGGGTTC | 221178 |
rs76965004 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107265 | AAAAAAAAAAAAAAA[A/G]CTCAAGCCTGGTTCT | 221178 |
rs76965375 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083539 | TGGAGTTGAAGGTGG[C/T]TGGAGGTTTGTTGGG | 221178 |
rs76978214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016644 | GTGGGGGTACCTCCC[C/T]GCTCCCTCTCCTTCC | 221178 |
rs76981615 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070143 | GTTCAGGAGCAGGGG[C/T]AGATTGTGGACTAAA | 221178 |
rs76984576 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004650 | AGGTGTGGTCAGCAC[A/G]GTGCATCAATTAAAT | 221178 |
rs76984587 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266579 | ATGAGCCACCACACA[A/C]AATCTTCAGTGTTTA | 221178 |
rs77010473 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076732 | CACAAGAAGAGAAAA[C/T]ACCTAGAGACAAAAG | 221178 |
rs77033524 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107885 | ATGCTCACTCGCACT[A/G]TTCTGGTGCTTCTCA | 221178 |
rs77045244 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987598 | TTGGTTATGCAATTA[C/T]GTGTTGACTAATTAG | 221178 |
rs77066479 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079604 | ACAGGGGGGTCCTGA[C/T]GGCTTGAGGGAGAGA | 221178 |
rs77078292 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076572 | CGAAGCAGCAGACCC[C/T]GGGACAGGAAACCAG | 221178 |
rs77130886 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114204 | TTTGGAGAGACTGCC[C/T]GCCAGTTTTTTGAAA | 221178 |
rs77140749 | snp | C/T | 0.350764 | 0.228794 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073019 | ATCCCGTAGATCTTG[C/T]CTCTATGAATTTATA | 221178 |
rs77175115 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071900 | TTAAAACAGCTGACT[C/T]GAGTGCTCTAACAGC | 221178 |
rs77190588 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063688 | TCTTCAGCTCAGGGT[C/G]AGGAGGAGGGGGCAG | 221178 |
rs77198390 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987960 | TCTTTTTTTTTTTTT[G/T]TGAGACAGAGCCTCA | 221178 |
rs77218736 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297911 | CACTTACAAGACAGA[C/G]CATGTCAGATGTAGT | 221178 |
rs77245367 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208050 | TGCCTGATGGGAGCC[A/G]CTGAAAGAGCTTTCG | 221178 |
rs77268932 | snp | A/G | 0.342582 | 0.232225 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028505 | TCTAATTAAATACAA[A/G]GTCCTATCTTTTCTC | 221178 |
rs77291503 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159448 | TTAGAGCAGTTTTAG[A/G]TTTAGAAAACAGGAA | 221178 |
rs77303408 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066471 | GCTTCAAGCCTAGGA[C/T]TCTTGCCATGGTAGA | 221178 |
rs77311210 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029780 | TCCCTCCTCCCACCC[C/T]CCACCCTCCGATAGG | 221178 |
rs77312865 | snp | A/C/G | 0.0368353 | 0.130617 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162635 | TGTTAGGTAGCATCT[A/C/G]CCAAACTCTGGGTGT | 221178 |
rs77318010 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122881 | GTAAAACAGTAGGAA[C/T]GACCTGTAAGCAGAT | 221178 |
rs77327016 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983683 | CAGAACTGAATTCTA[A/T]ATCTAGCTTGCTTCA | 221178 |
rs77329609 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278978 | TCCCTCCTTCCCTCC[C/T]TCCCTCCCTCCCTCC | 221178 |
rs77341506 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121035 | TTTCTTTTTTTTTCT[A/G]AATTAAGTTCTTTTA | 221178 |
rs77346079 | snp | C/G | 0.130008 | 0.219321 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272683 | GTGTGAGTTGAAGCC[C/G]AGCCTGAGACAGGCT | 221178 |
rs77370399 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245080 | GAAAGACTCTTTAGA[A/G]GACATGGCTATGCCC | 221178 |
rs77373202 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150562 | ATTGATTTTTTTTTT[A/T]AAGGAATTGCACACA | 221178 |
rs77394122 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051030 | GCTAAGCAGGCTATA[C/G]ACCCATATCTGCCAT | 221178 |
rs77397451 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099473 | GCACACTAGTGGCCG[C/G]CCTGTGGGGCAGTGC | 221178 |
rs77409416 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233636 | CAGTTTAAAAAAAAA[A/G]GTTTCCATTTGCTCT | 221178 |
rs77430965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139417 | AAATACAAACAGGAC[A/G]TTCTGACAGAGAAGA | 221178 |
rs77434528 | snp | A/C/G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205029 | CCTTGAAAACCGACA[A/C/G/T]AAGACAAGAATGGCC | 221178 |
rs77440624 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044853 | AAATATCCATCTCCT[A/G]GAGACAGTAAATAGA | 221178 |
rs77449781 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023109 | CCCACCCCATGACAG[A/G]CCCCTGTGTGTTATG | 221178 |
rs77461881 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286596 | TTTCTCTGTGGTCCT[C/T]GTGCCTGCTGGCATA | 221178 |
rs77465364 | snp | C/T | 0.264358 | 0.249587 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029374 | TTACATTTTTTTAGA[C/T]AAATAGTGTGAAATC | 221178 |
rs77468967 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061309 | GTAGAAAGTAATGTA[A/G/T]CAATTCTTCAAAGAG | 221178 |
rs77473075 | snp | A/G | 0.343254 | 0.231956 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034862 | CTGAGCTGACAATGG[A/G]CACAGCACCACTCTG | 221178 |
rs77473723 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052465 | CTTTCATTCAGGGTT[C/G]TAACTATTGATAAAA | 221178 |
rs77490749 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026144 | GGTTGCAAATATATT[C/T]CCCTCAAAGTATGAT | 221178 |
rs77501405 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231501 | CTTTGTTATCTGTTC[A/G]TCTGTTGATGGAGAT | 221178 |
rs77513503 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260776 | TTAAAGAAGCCAGAA[C/T]TGGAAATCATAGCGG | 221178 |
rs77522333 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069638 | GATTGCCCTGGCCAG[A/G]ACTTAACTTTGTTTT | 221178 |
rs77523337 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016683 | AGTTTCCTGAGCTGC[A/G]TGTCCCCAGTGTTCT | 221178 |
rs77541178 | in-del | -/TGTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025191 | ATATTTTCCTATTTT[-/TGTTT]ATTTCCTAAAATTTT | 221178 |
rs77570374 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145047 | CATTGTGAATATAGT[C/T]AGAATGAGCTGGTAC | 221178 |
rs77572366 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070686 | AGACTGAGTGAAGTC[A/G]ACTTTCCTCCCTAAT | 221178 |
rs77588305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107827 | GTACTGCTCTATCGG[C/T]ACGTTAAATCTAGGT | 221178 |
rs77590019 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288768 | TTCTGGAAACATTAT[A/G]TGGTTTATTGGATCC | 221178 |
rs77593726 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234435 | CCTCTTCTATATTTC[C/T]CTTCTTGAACTTCTC | 221178 |
rs77596724 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080110 | TGAATTATGAAGAAA[A/T]TACTTCTTGGGTCTT | 221178 |
rs77598857 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004563 | CCCCTTATGAAGGTG[C/T]TCCTTCCTTGGGAGT | 221178 |
rs77599100 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044016 | GCATTTTGCTTTTCA[C/G]AGGGTGCTCTGAGCA | 221178 |
rs77604897 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989757 | AATCTAACCCCCAAT[A/G]TGATGGTATCAGAAG | 221178 |
rs77645743 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036016 | AAGACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 221178 |
rs77647417 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267918 | AAACCTGAATGTGCA[C/T]TTGAATAACCTGGGA | 221178 |
rs77653886 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043341 | TGTGGTCAAACACCA[C/T]GTCCACTTCTCCCAT | 221178 |
rs77681751 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269344 | TTACTAATTGGCACT[A/G]TCACTTGTTTAACAT | 221178 |
rs77683209 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024381 | GATGGATGGATGGAT[A/G]GATAGATGGAATGAA | 221178 |
rs77684704 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128272 | GAGGGGTGACCTACA[C/T]GTGGGACAGGAAAGG | 221178 |
rs77695853 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114644 | CTCCTTAGTTTTTTT[G/T]TTGTTGTTGTTTTTT | 221178 |
rs77697157 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244209 | TTTCCCTCTGCATCA[C/T]AAGGACACCAGCCAC | 221178 |
rs77739156 | snp | G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257624 | TACTTTTTTTTTTTT[G/T]GGCAAATATAGTTCT | 221178 |
rs77760857 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222757 | GCGTGCCTCTTCTTC[C/T]GTGAGCAGAGGGGCT | 221178 |
rs77762812 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045438 | TCTCTCAGTTTAAAT[A/T]GCTGCGACATGAAAA | 221178 |
rs77784335 | snp | A/C | 0.192715 | 0.243348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280952 | CGTTGTTCAGGCTCC[A/C]GTGTTTCTCAGACAG | 221178 |
rs77787047 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095244 | TTTCACAAAAAGAAG[A/G]AAAGCCTGTTACATG | 221178 |
rs77788252 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261215 | CGGAAAATGATAGTG[A/G]CACTGGAGATATGAA | 221178 |
rs77792538 | snp | A/G | 0.0314385 | 0.121371 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162062 | CACTGCATTATTCTC[A/G]GGGTGCCTGTCATGC | 221178 |
rs77804905 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169748 | AGGGAAGAAGGTAAC[C/T]TCCTGCAGACCTTTC | 221178 |
rs77817090 | snp | A/G | 0.275999 | 0.248644 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978216 | TGGCCTGTGGCCATT[A/G]ATTTTTAATTGACCA | 221178 |
rs77826356 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036014 | GTAAGACCCTGTCTC[A/C]AAAAAAAAAAAAAAA | 221178 |
rs77833614 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074313 | CTCAAGATTCATCCA[C/T]GTGGTAGCATGTGCT | 221178 |
rs77846072 | snp | A/C | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073891 | CCAGTTACGTAGACC[A/C]AGACATAAATGGAAA | 221178 |
rs77849023 | snp | A/G | 0.375 | 0.216506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205088 | TGCCTGATTGCCCTG[A/G]CCAGAACTTCCATTA | 221178 |
rs77857899 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030745 | TTTGTTCCTTTAAAA[A/G]AATATATTGACTCTA | 221178 |
rs77858804 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087430 | TTTAGTCGAAGACAC[C/T]GGGAGAAAGTAGATT | 221178 |
rs77885604 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207603 | GTTATTTTCTGTTTT[C/T]TTAAGGTAACAGGCT | 221178 |
rs77897667 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295272 | TTATCTTATAAATTG[A/G]GGAGGAAAATATTAC | 221178 |
rs77913337 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083720 | AAGGGGAGTCACTTT[C/T]CAGACAGAAAGACTG | 221178 |
rs77914940 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005730 | TGTAGAGGGGCATTT[C/T]CTGAGGAATGCATGT | 221178 |
rs77922671 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231371 | GTGGTCTTTTGTGAC[C/T]GGCTTCTTTCACTGA | 221178 |
rs77923234 | snp | C/G/T | 0.0314385 | 0.121371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208436 | TGTAATTCATAATCC[C/G/T]CAGTGCTCCTAGCAC | 221178 |
rs77936980 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235330 | GCAAACTTTGAGATT[C/T]GCTGTCCAGGCTGAG | 221178 |
rs77952630 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200120 | TACAAACCCCTTCAA[C/T]GGGCATTTTCTTAAT | 221178 |
rs77963271 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145750 | AAATAGAGAACGGCT[A/C]ATTTTCAAATTGGTG | 221178 |
rs77971723 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986694 | TTTGCTCCTTTGTGA[A/G]ATAGCATTGTCTTCA | 221178 |
rs77985129 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052836 | GCCGCCAGGGGATCC[C/T]CCCCGCCACTGTGCC | 221178 |
rs78008132 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117057 | TATTATTTAAGCCAC[A/G]CAGTCTATGGAATTT | 221178 |
rs78014444 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073416 | ACAATATAAATATCT[A/G]TCTATACCTATCTGT | 221178 |
rs78020046 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012811 | ACCACCCTGAGCCCC[A/G]TGGCTGCAGACAGTG | 221178 |
rs78034788 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200537 | CCAAGAGGTGACATC[A/G]TTCTGACTTCGGGGA | 221178 |
rs78044119 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045697 | TTTGTTGTGAAGAAT[C/T]GCCAAGCAAGTCCTA | 221178 |
rs78045275 | snp | A/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072064 | AAGTGCACATGTCCA[A/T]TCAAGAATATTAAGG | 221178 |
rs78058662 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019517 | TTACAGATCCATTAC[C/T]TAGCCAAATATTTAT | 221178 |
rs78059923 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044236 | TTTTCTTTCTTTCTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs78070828 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030433 | TCAGTAGGGTGCTTA[C/T]GCTCTCCTTATTTGA | 221178 |
rs78074952 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070609 | GTGCTGATATTTGGT[G/T]GAACATTATTCTGTG | 221178 |
rs78075726 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069676 | CTTAATTTTACATTC[A/C]AGGGGTGCATGCCTA | 221178 |
rs78082065 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233637 | AGTTTAAAAAAAAAA[G/T]TTTCCATTTGCTCTG | 221178 |
rs78100459 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073123 | CCATTTTCTGGATAA[A/C]GTCATGATCATTAGG | 221178 |
rs78102326 | snp | A/C | 0.0948562 | 0.196037 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106056 | AAGAAGATTTCTTTT[A/C]TTTTCTTTTCTCTGT | 221178 |
rs78103920 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054646 | GAACTCTAAAGAGTA[C/T]AGAAGAGAAAATATG | 221178 |
rs78104377 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299990 | TTTGTTCAGGGTGGA[A/G]CTGCTAACGTGCAAA | 221178 |
rs78117675 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047434 | TACAAAGGCAGTTTC[A/G]GTCCCTGAGCAAGGA | 221178 |
rs78139914 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031167 | TGCTTAGAACTGCTG[C/T]GGAGGGGAGGCCCTT | 221178 |
rs78143637 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018470 | TAAATTCCTTTTTCT[C/T]CAATTAAAGTGGAAC | 221178 |
rs78150092 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178417 | TTTAACTGTAAGAGC[C/T]TTTTTGACCATTATC | 221178 |
rs78170937 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147119 | ATTGTTCAGATAATT[G/T]TTTTCTTACCATCAA | 221178 |
rs78190328 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205114 | AGGCAAGAGAAATAA[A/G]TAAAGGGTATTCAAA | 221178 |
rs78200408 | snp | C/T | 0.116138 | 0.211142 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111856 | TCACTATTTTGCCTC[C/T]GGGCTTATAATGCAG | 221178 |
rs78200671 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272668 | CCTGTTCTCCTGTCA[C/G]TGTGAGTTGAAGCCG | 221178 |
rs78236964 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039935 | GCCACTCACTCCTGT[A/G]TATGGTGAGGGCCTT | 221178 |
rs78239498 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163654 | ATACTGAAGCAGAGC[A/G]TGCACCTTGATAGCT | 221178 |
rs78245096 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033748 | CCTCCACCTGGCTGC[A/G]TGTCCCTCCGTCATG | 221178 |
rs78259204 | snp | A/C | 0.13446 | 0.221699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246538 | CGTTTGTGCGTGTCT[A/C]TGTGTGTGAGAGACA | 221178 |
rs78266197 | snp | A/G/T | 0.00954734 | 0.0685228 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062217 | TAGTGATGCTATTCC[A/G/T]GGAAGAGCTCTAGGG | 221178 |
rs78270872 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089155 | ATAACGGAAGCACAC[C/G]TAGGAAGAGTTTCTA | 221178 |
rs78272775 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230948 | CAGCTCTGTAGAGAG[G/T]TCTAATTTGCATAAC | 221178 |
rs78273838 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251026 | AATAAACAAAAGAAG[A/T]AAAAAAGAAATCTAA | 221178 |
rs78298365 | in-del | -/C | 0.316 | 0.241131 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131927 | TAACAGCTCACATAT[-/C]CCCTCAGGGTACCAA | 221178 |
rs78301440 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114240 | CAAAAGAACAATTGA[C/T]ATTCCTCTTTGTGGG | 221178 |
rs78318055 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090424 | CACCTCAAACACAAC[C/T]ATCTAAGGTTAACTA | 221178 |
rs78323399 | snp | A/G | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255695 | GAGATGCAGCCCAAG[A/G]GGTGGTGAGACTCAC | 221178 |
rs78327521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126173 | TCTGCCCTCACTTGC[C/T]ACAGGGACTTCCTCT | 221178 |
rs78336345 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993733 | GAAGCATCCAGGCTT[G/T]CTTTTTAAGGGGATC | 221178 |
rs78339813 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148868 | GACACAGGAGCTGCT[G/T]TTCATTCTGGTAGAG | 221178 |
rs78352354 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240272 | TTTAAAAAAAAAAAA[-/AA]TTACAACCTACCAAT | 221178 |
rs78365690 | snp | C/G | 0.119978 | 0.213528 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016194 | TCCTTCAACCCCACT[C/G]CTGGCTCCTCCTGTG | 221178 |
rs78375657 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298644 | AGCCCTCAAAAGTCA[G/T]GGTCCAGGACGGAGG | 221178 |
rs78384903 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156791 | ACAGATAAGGAGCCG[C/G]TCAAAGTGAGGTTAT | 221178 |
rs78389711 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052408 | AACAAACTATTATTT[A/T]AAAAATAAAAATAAA | 221178 |
rs78392586 | snp | A/G | 0.222333 | 0.248464 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054565 | TAAATTAACTTTGAC[A/G]TGTAGCAGCAATTCA | 221178 |
rs78398541 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097775 | CCAAAGGTATGCACC[A/G]GAAAGCATGGTACAA | 221178 |
rs78418726 | snp | G/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977792 | AACTTTTTGGCATAG[G/T]GTTGCTCACAATTTT | 221178 |
rs78423977 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077267 | GACTCCATGTCAAAA[A/C]AAAAAAAAAAAAAAA | 221178 |
rs78426153 | in-del | -/G | 0.36315 | 0.222928 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117683 | AAAGAGAAATTAAGA[-/G]GRAAAAAAACCCCAA | 221178 |
rs78431479 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210352 | CTTATTGCCAAGACC[A/G]GTGTCAAGGAGCTTT | 221178 |
rs78444622 | snp | A/C | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093532 | ACGTTTCTGATACAC[A/C]CCAAAAACAGCTGGA | 221178 |
rs78453962 | snp | C/T | 0.404907 | 0.196224 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182357 | AAGAGGTTAAATTGG[C/T]TCACGGTTCTGCAGG | 221178 |
rs78467468 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037759 | GCAGAAAAATTGATC[A/G]GAGTTTCTTAATCTG | 221178 |
rs78469742 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004686 | CCGAGACTGCTCCAT[A/T]CACACAGGGCTGAAA | 221178 |
rs78492277 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087466 | CCTTAGCTATGGACA[A/G]CATCCAGAGACTTAA | 221178 |
rs78498154 | snp | A/C | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066683 | TCTGTTTTCACCCCT[A/C]AGGCCCCCCACCTTC | 221178 |
rs78501242 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186828 | AGCTGGAAATAGGAT[C/T]GGAAATCCTAGTGTG | 221178 |
rs78506514 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182511 | GAGAGAGAGAGAGAG[A/C]GCAGGAAAGAGGATG | 221178 |
rs78519278 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249960 | TCAAGGGCGGCACCA[C/T]GTACTTAACCACCTT | 221178 |
rs78519490 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006781 | TCCTGGTGCCCTTGC[A/G]TTCATGTGCCAGCTT | 221178 |
rs78524020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980036 | TTTTTTTCCTGAAGT[A/G]GGGGGTGAAAGTTGA | 221178 |
rs78526634 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193999 | AAAAGAGTTTGTAGA[A/G]GTTTCTTACCTTCTC | 221178 |
rs78538093 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214839 | GATTCAACATATTTA[A/G]GTATTAGTGATTCTT | 221178 |
rs78545278 | snp | A/G | 0.265727 | 0.249505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030559 | TAATATTAAAGCCCC[A/G]GCCCCAGAGCCTAGA | 221178 |
rs78572378 | snp | A/C | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977697 | TAATTTGTTGTAGGG[A/C]AATCTGGGTCTTCTG | 221178 |
rs78578468 | snp | G/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173525 | ACTTTTTTTTTTTTT[G/T]GGCCTTATTGCATTG | 221178 |
rs78578529 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064132 | CCTGTTCTCCTGCCT[C/G]ATCAGGCCACTCCAG | 221178 |
rs78587295 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034245 | TAAATTTCAAACCTC[A/G]GGGAACCTTCTTTGT | 221178 |
rs78596496 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247465 | CCACACTGTGCTCTT[C/T]GCTCCACATTCACTT | 221178 |
rs78597895 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045865 | TGTGTGGTCTCAGAT[A/G]AACTGATTCCATTCT | 221178 |
rs78606354 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007092 | GCTGAGTGTGACCTT[C/T]CTGCTGGCCCTTAGC | 221178 |
rs78606488 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178396 | TCTGAGGAACATGCA[A/T]TTTTTTTTAACTGTA | 221178 |
rs78617349 | snp | C/T | 0.093777 | 0.195178 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003152 | GTAGCATTTTCCCCA[C/T]GCTGGTCTATAAATG | 221178 |
rs78624273 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070610 | TGCTGATATTTGGTT[C/G]AACATTATTCTGTGT | 221178 |
rs78627884 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233178 | CATTTTTTTTCTGAC[A/G]AAAACATTACAGAAT | 221178 |
rs78628565 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072171 | TGTGTTCTTAGAATG[C/T]AAAATGGCTTGTAAC | 221178 |
rs78635306 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085651 | GACTTTACTCACTTC[C/T]ATGTGGCCCGACTCC | 221178 |
rs78637135 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178893 | TTGAAGACATTTTCA[G/T]CCCCTCCGAAAGGAA | 221178 |
rs78648095 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176050 | GTCTGCTGGGTACTG[A/G]AGCAGGCGTGGGGGA | 221178 |
rs78658354 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051128 | CACTGAGCAAATGAA[C/T]TCCAAGTGAGCACTG | 221178 |
rs78660322 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036851 | CACAATCTCGGCTCA[C/G]TGCAACCTCCACCTC | 221178 |
rs78674330 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004263 | TTTGCTCTGCAGTCA[G/T]CAGTCAATAAAGAGT | 221178 |
rs78683705 | snp | G/T | 0.163892 | 0.234703 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254699 | TTTCCGCAAGGGGCT[G/T]TCTGGTTCCTGCGGG | 221178 |
rs78692036 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271981 | AAAAGGAAAAAAAAA[G/T]TTGCCTGGCGATTTC | 221178 |
rs78700101 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145912 | GAAGGAGCCTATTCC[A/C]TATGTGAGAAAGAAG | 221178 |
rs78740051 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256491 | TAAAATAATAATATA[A/G]AAAACTCTCCAAATT | 221178 |
rs78741320 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166449 | AGGAAAACCTTCTAG[C/T]CCTGGGGGACGGCGT | 221178 |
rs78764725 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042340 | AAAATTAACATAAAA[C/T]GTAAAAGTTCAAGTT | 221178 |
rs78775566 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127582 | AAGAAATGAGATGAC[A/T]GTGATGAGTCATTCA | 221178 |
rs78791679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249437 | TTTCTTTAATACCTT[C/T]CTGGATATTGAGCTC | 221178 |
rs78808673 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116010 | GTCTCAGAAGTCACA[C/T]GCCATCATTTCTGCA | 221178 |
rs78810633 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140242 | GTTTAGGTTAAAGTT[A/C]ATTTATATTCAAATC | 221178 |
rs78835093 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157910 | CTTCTAACTTCATTT[G/T]CCCCATATATAAAAT | 221178 |
rs78858996 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251223 | CTCCACAAATCCTTA[A/C]TGAGGGCTCATCTAT | 221178 |
rs78860540 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110834 | GATAAGGAAGTTAAG[A/G]ATAAACACCAAGGTT | 221178 |
rs78864513 | snp | A/G | 0.0240643 | 0.107019 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304030 | CACTCTCAAAGAGCC[A/G]CACTGCTCCTGACAT | 221178 |
rs78869042 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259479 | AAGGCTCAGTGGTTT[C/T]AAAGTACAATTGGGG | 221178 |
rs78876366 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180171 | GTGCTCTATTTTGCA[C/T]ATGGTGTAAGGGAAG | 221178 |
rs78885470 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092716 | TTCCCTTTCAAACTG[C/T]CACATTTGGCAGCTT | 221178 |
rs78906784 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101484 | CTATTTTTTAAATTG[C/T]GGTGAAAAAAAACAA | 221178 |
rs78914104 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287695 | GTCATATGAAAGGCT[A/G]TATTCTATTGTCATG | 221178 |
rs78916128 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226017 | TAGGAGACCTGGAAT[A/G]TGTTGCTCCTCTCTG | 221178 |
rs78917072 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984962 | CGTGCACATCACATG[A/G]CACAGATTCAGGAGG | 221178 |
rs78933226 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081266 | GGACAAAAAGTGAAG[A/G]GTTGAGTTAATCATA | 221178 |
rs78949968 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301961 | TTGGGGAACCAAGGC[A/G]TAGAGAAATCATATC | 221178 |
rs78951179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246911 | TTTAAGCAGTATGTG[A/G]CATCTTACTAGGCCG | 221178 |
rs78957625 | snp | G/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219448 | TGAGTGTTAGAAAAT[G/T]TCAACTTCTTCACTC | 221178 |
rs78970602 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199855 | GTAAGTAATTGTAAT[C/T]CAATTTTTTAAAACC | 221178 |
rs78972841 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250309 | TCTTATTTTTTTTTT[G/T]AGTTGCAACTTTGCA | 221178 |
rs78976376 | snp | A/T | 0.0966517 | 0.197444 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230664 | AGCTGAGGTGATGTG[A/T]GGACTTAACATGGGG | 221178 |
rs78997458 | snp | A/G | 1.67175e-05 | 0.0028911 | missense | SPATA13 | GRCh38.p7 | 13:24284186 | TGGATGACAACGGTA[A/G]TGAGGAGGACTTCAG | 221178 |
rs79006567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144719 | GACTTTGGCCAGCGT[G/T]GCGTAGTTGGTGTTT | 221178 |
rs79008071 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069591 | CCATCCTCTCTCCCT[A/G]TGTGGATGCCCTTTA | 221178 |
rs79008302 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014368 | GCAGAAATGGCCCCA[C/T]TGTTTCTGGGGCCTT | 221178 |
rs79008919 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093922 | TCAACTGTAATCAGA[C/T]TATATACCTCAGGCC | 221178 |
rs79022616 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069984 | TGAGATGTGGGAGTG[C/T]GGTAGAGGGGTCTCT | 221178 |
rs79029383 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184330 | TGTACCCAATAATTA[C/G]TTACTTATTGTACCC | 221178 |
rs79064212 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069787 | TCATGTAATATTACC[A/G]GTTCAATAATTCTAT | 221178 |
rs79068837 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202999 | TATTTTAAGTTCCTG[A/G]GTACGTGTGTAGGAT | 221178 |
rs79086520 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219005 | TTCTCATTATCACCA[A/C]AAAAAAAAAAAAAAA | 221178 |
rs79099781 | snp | C/G | 0.317451 | 0.240729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209075 | CACTGTTGATGAGCT[C/G]TCAGCACTGATGCAG | 221178 |
rs79102548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092808 | TTTGGGCATCTGTAT[A/G]TGGAGCTTTTATACT | 221178 |
rs79104809 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197112 | TACTGTTCCAGTTTT[A/C/T]ATTATGTTTCAGTCT | 221178 |
rs79107134 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231068 | TGGCTCCCCCCAGAA[A/G]GCTTCCCCACGCCTT | 221178 |
rs79116575 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150126 | GGTGGACTGATGGGG[A/G]ACAGTCACATTAGAA | 221178 |
rs79149851 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107045 | CAACATGAAAAGATG[A/G]TAAGGACGGGGAAAA | 221178 |
rs79150846 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063316 | TGACAAATAAAAATT[G/T]TATGTGTTTATCATG | 221178 |
rs79180307 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211507 | TGTATCTGTTGAGAT[A/T]GTCCTATGATTTTTA | 221178 |
rs79194665 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24264057 | CTTAGCTGTTGTTTC[A/C]TGCCTCATTGTTGCC | 221178 |
rs79203507 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992179 | AAAGTGGAGAACTGC[A/G]GTCCAACCATGTGCT | 221178 |
rs79211623 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010460 | GGGAGGTATGTAGCT[C/T]TTTTTTTTTTTTTTC | 221178 |
rs79214545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062054 | AGGTCCAGAGGTGTT[A/T]TGTGCGATGGAAGCG | 221178 |
rs79217202 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983646 | ATATTCTGTTGGTTG[G/T]TTTTTTTTTTTAAAA | 221178 |
rs79223075 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245230 | GAATCGCAACCAAAC[C/T]ACATTCCCTGGAATG | 221178 |
rs79251576 | snp | A/C | 0.0711525 | 0.174681 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187444 | GGATGTGGAAAACAG[A/C]GACCGGCTTACGTTT | 221178 |
rs79278310 | snp | G/T | 0.0573587 | 0.15934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257587 | TACTGAAGTAATTGC[G/T]CAATTTGATTTTTTA | 221178 |
rs79284638 | snp | G/T | 0.00278618 | 0.03722 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224470 | CTCAGAGAGAGCCAG[G/T]GCCTGTGTCCTTGCA | 221178 |
rs79288970 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044252 | TTTTTTTTTTTTTTT[G/T]AGACGTAGTCTTGCT | 221178 |
rs79296611 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003487 | ACAAAGCAAGTAATG[C/T]GTAATTTTTTCTTTG | 221178 |
rs79313076 | snp | C/T | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255593 | CATGGAGGACCAGGT[C/T]TGCATTGCAGTGGAA | 221178 |
rs79317645 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285137 | TGTGTATCGTTGGGC[A/C/G]CTAAGGAGATGGGCA | 221178 |
rs79326019 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226015 | CATAGGAGACCTGGA[A/C]TGTGTTGCTCCTCTC | 221178 |
rs79342720 | snp | C/G | 0.0898077 | 0.191933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216016 | CAGGCCATGGCTGTA[C/G]GAAGTCAAGACGCAG | 221178 |
rs79355046 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180404 | TCCTGTGGCTTTATA[A/G]TAAGCTTTGAAATTA | 221178 |
rs79368849 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057070 | TTCTTTTTTTTTTTT[C/T]TTTTTTTAAAAAATT | 221178 |
rs79369392 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030176 | GATGAACCAACACTG[A/G]CACATCATTGTCACC | 221178 |
rs79371470 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220517 | CTTCTAGAGCACATG[A/G]GGTTGGATAGGTGAT | 221178 |
rs79380529 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157447 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 221178 |
rs79400694 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124406 | AGTCGAGGTGTAGAG[C/G]CCCGTCAGTGTCTAA | 221178 |
rs79403644 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273745 | TATAGAACATCAAAG[G/T]CAGATATTGTTATGG | 221178 |
rs79409935 | snp | C/T | 0.00892191 | 0.0661918 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223919 | CAATGTGACTGAGGC[C/T]GCCTGGAGGAGGGAG | 221178 |
rs79411807 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990287 | TGTAAAACCATATCC[C/T]TGGCCAAAACCCTTT | 221178 |
rs79445263 | snp | A/T | 0.0573587 | 0.15934 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256374 | GATAAGTGCTTGGGG[A/T]GATGATATGCTAATT | 221178 |
rs79446363 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096142 | TCATTGGGATCCTAC[A/C]ACCTGCCTGGTGCCT | 221178 |
rs79478800 | snp | A/C/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072935 | AGCCCATATGTGAAA[A/C/G]CCAGGTAAACTCGCA | 221178 |
rs79488872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057626 | TTGTTTTCTCTCCAC[A/C]CTACCCCTATCCCCA | 221178 |
rs79503433 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284698 | CACTGTGATTCTCTG[A/G]CCTCGTCCAGGAAAA | 221178 |
rs79533144 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081523 | CTTACTAAAAAAAAA[A/C]GCTGGCCCAGTGTGA | 221178 |
rs79540826 | snp | C/T | 0.00912582 | 0.06693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224625 | TGGGCGACCCTCCTG[C/T]GGGAAGGGAGCTTGC | 221178 |
rs79542632 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299728 | AGGAAGGCTTCCCGC[A/G]GGAGAAGGCAGGGCC | 221178 |
rs79557688 | snp | A/G | 0.230896 | 0.249269 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046601 | GCAAGATTCATCCAT[A/G]ATGTGTGGGTAGCAA | 221178 |
rs79563900 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221852 | CTCACTCACTCTGTC[A/G]CCCAGTTTGGAGTGC | 221178 |
rs79573361 | snp | C/G/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071875 | CAAGATGATTCTCCC[C/G/T]GTGTGCACTTTAAAA | 221178 |
rs79585348 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146250 | ATAGATCAGCTTCAG[A/G]GACTGAAGCCAATTA | 221178 |
rs79595411 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120205 | CCGCCTCTGAAAAAA[A/G]AATCAGGATTCTACT | 221178 |
rs79616031 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069936 | CAAAGGAAGGTCCCC[A/G]ATGTGAGTTCACTCT | 221178 |
rs79630691 | snp | A/C | 0.141596 | 0.225274 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083216 | TCAGCCAGTGGAGAC[A/C]CCCTAGGGCAATAGA | 221178 |
rs79649370 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118923 | TTTCTTTTTTTTTTT[G/T]GAGATGGAGTCTTGT | 221178 |
rs79650548 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210199 | CTTTACTTGTTATAT[A/G]ACTTGCACATGTTTT | 221178 |
rs79669064 | snp | C/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219115 | TCTTAGTTCTGTTCT[C/G]TTCCTATCTCTGGCA | 221178 |
rs79673995 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190957 | CAGCAAACCTCACTG[A/T]CTTCTCATTTTAAGA | 221178 |
rs79684731 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141447 | TTCCTGCTTCCCTCC[C/T]ACCTGCTGTGCCTGA | 221178 |
rs79687335 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219453 | GTTAGAAAATTTCAA[C/T]TTCTTCACTCTATAA | 221178 |
rs79688450 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221588 | GGACAAGATCTGAGG[A/G]GAAGGGATGGACACA | 221178 |
rs79690499 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275070 | CCTGATGTCTTCTCT[A/G]ACTGTATTTGTAACA | 221178 |
rs79711232 | snp | C/T | 0.0596104 | 0.162024 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270615 | CCTTAGTTTAGAATT[C/T]TCTCCTGAAGTCCCC | 221178 |
rs79720032 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046892 | TTCACTGAGACAGCG[C/G]TATTGCAGTAGAGAA | 221178 |
rs79720700 | snp | C/T | 0.0946025 | 0.195836 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103348 | AGTATAGGCTGGGTG[C/T]GGTGGCTTGCACCTT | 221178 |
rs79731860 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150146 | TCACATTAGAACATG[A/G]TGGGCCAGACCCTCT | 221178 |
rs79738425 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059757 | TTTGGGCCTGAGACT[A/G]TGGCGTTTCCTGGAT | 221178 |
rs79763908 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248118 | GCAGGGCTTACAGGC[C/T]TCCACTCCTGCAGGT | 221178 |
rs79806102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186958 | AAGAGCCTCATTATG[C/G]GTCAGATGTGTAGGT | 221178 |
rs79807540 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078817 | GGCTTGCTCATTCAT[C/T]TATTCATTCATCCCC | 221178 |
rs79845721 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146645 | AAATGCACAGCAATT[A/T]AAAAAAAATGCCAAT | 221178 |
rs79855953 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129179 | GAAAAAAGGAACTGT[C/T]CAGACTCTGGTGCTA | 221178 |
rs79857099 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993987 | TTTTTTTTTTTTTTC[C/T]TTTTTTTTTTTGACA | 221178 |
rs79866149 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984306 | TCACCAGTCATCAGA[A/G]TCTCAAAGTACTTGT | 221178 |
rs79870109 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061417 | AAGCCACATGCATAC[C/G]AATGCTCATTGTAGT | 221178 |
rs79878042 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222285 | CAGTTAGTGTTTGGG[C/T]GTCTCAGCCCTCCTG | 221178 |
rs79898602 | snp | A/C | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159110 | AGAGATAATAAAAAA[A/C]CCCTCAATTTAGACC | 221178 |
rs79904125 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095024 | AGTTAAAAATAGAAT[C/T]GCCATGTGATCCAGC | 221178 |
rs79911946 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070612 | CTGATATTTGGTTGA[A/G]CATTATTCTGTGTGT | 221178 |
rs79933872 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024389 | GATGGATGGATAGAT[G/T]GAATGAAGGAATGAT | 221178 |
rs79959854 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253733 | GCTGGGGACAGGTGA[A/G]TAGGAGGCAGTGAGG | 221178 |
rs79964850 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017296 | ATAATTTGCCTGGGC[A/G]TGCAGCAAGTGAGTG | 221178 |
rs79971353 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269924 | ATAGGGTCTTGCTAT[A/G]TTGCCCAGACTGGTC | 221178 |
rs79987004 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046744 | AAGCTTATATGAACA[C/T]TCTTGTACATCTTTG | 221178 |
rs80006698 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166194 | ATCTTTTGTGTACTA[C/G]ATGCTGAAGATGGAG | 221178 |
rs80007660 | snp | C/G | 0.316726 | 0.240931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209584 | TTTATCAGTGTTGCT[C/G]CAAATGACAGGACAT | 221178 |
rs80009166 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141664 | TCCTTGCAGCCCAGC[A/G]CCTGCCACGCAGGGG | 221178 |
rs80010772 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114390 | GCACATGCGCGTGTG[C/T]GTGCATGTGTGCACA | 221178 |
rs80015236 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037921 | CAACTAGACTAGATT[C/T]TTTTTTTTGAAATGG | 221178 |
rs80020643 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135130 | TCTCAACTCCAGAGC[C/T]GCAGGAAAATAAATT | 221178 |
rs80023477 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001123 | GCCGAGTGGCCTCTT[A/C]TACTCTCACCCCCTA | 221178 |
rs80035269 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021730 | TCTTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 221178 |
rs80050990 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065283 | AACTTCCCCCATGTG[C/T]TGAGCTTCAGAGTGG | 221178 |
rs80059153 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006526 | GGAGGCTCAGGGCAC[A/G]AGGTGCGGCAGAGGA | 221178 |
rs80073311 | snp | C/T | 0.0359798 | 0.12921 | missense | SPATA13 | GRCh38.p7 | 13:24249790 | CCGTGATAGGTGGGG[C/T]CAGCTTGTATGGGAC | 221178 |
rs80083105 | snp | A/G | 0.11963 | 0.213316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272894 | CACATTAAGATGCCA[A/G]GAAGCCGGATGGGTG | 221178 |
rs80083842 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112715 | TCATCTACTTTCTCA[A/G]TCTTGATCCACAGTT | 221178 |
rs80084470 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114073 | GTTTCTTATTAGTGC[C/T]TATCTAAGAGGTGCA | 221178 |
rs80088429 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284933 | TAATTACTGGCTGGC[A/G]AATGGCAGAGCTGGA | 221178 |
rs80099434 | snp | G/T | 0.116838 | 0.211584 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188808 | GTCTGGTTTCAGAGC[G/T]TCAAAGGACACAATG | 221178 |
rs80142035 | snp | A/G | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256371 | AATGATAAGTGCTTG[A/G]GGTGATGATATGCTA | 221178 |
rs80142468 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178876 | CAATTACCATAGTCA[A/G]TTTGAAGACATTTTC | 221178 |
rs80146368 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071540 | TCCTCAATCGCTTCT[C/G]TCTGGTGGAACTAGG | 221178 |
rs80152419 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205223 | AAAATCTCCTTAAAC[C/T]GATAAGCAACTTCAG | 221178 |
rs80160409 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140070 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 221178 |
rs80170652 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297910 | GCACTTACAAGACAG[A/T]CCATGTCAGATGTAG | 221178 |
rs80175379 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110384 | AAACCTTGGGAGGGG[A/T]CTGCATTTTAGGACT | 221178 |
rs80181697 | snp | A/T | 0.104859 | 0.203554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218733 | TTGCGATTTTTTTTT[A/T]AATCTCATCAGCAGT | 221178 |
rs80212114 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023396 | TAACTGATTTGGATA[C/T]TTTGCTTTTTATCTT | 221178 |
rs80243664 | snp | A/C | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068405 | AGGTTGATTCCATGT[A/C]TTTGCTATTGTTAAT | 221178 |
rs80265846 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216406 | TGTTTTAGCCCAGTA[A/G]CCCCCATAAGGCAAG | 221178 |
rs80267911 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140135 | GCTCCTGCCAATGCT[A/C]ATAACCTAGGACTGC | 221178 |
rs80274457 | snp | A/C/G/T | 0.00398755 | 0.0445055 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240807 | CCAGCTGTGTTTTTC[A/C/G/T]CATCTTTTATCATCC | 221178 |
rs80278680 | snp | A/G | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977649 | CCAGCCTGGGCAAAA[A/G]AGTGAGACACTGTTT | 221178 |
rs80283235 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24072823 | TGTCTACTGTTGGCT[-/TT]CCTTTTTTTTTTTTT | 221178 |
rs80301290 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032395 | ACAAGTGTCATGGGA[A/C]TATTTCTTCTTAAAC | 221178 |
rs80328385 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086031 | GGTTAGAGGACATCT[C/G]TTGCCAAGGTGAGTA | 221178 |
rs80341005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992979 | AGCCAGCTGTGCCCT[A/G]AGAGCTGCCTGTCAT | 221178 |
rs80342889 | snp | C/G | 0.0839998 | 0.186933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150160 | GGTGGGCCAGACCCT[C/G]TGTCCTGAGACACAT | 221178 |
rs111216630 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189985 | ATATATTATATAAAT[A/C]ATTATATAACATATA | 221178 |
rs111216652 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190110 | ATATACAATATATAT[C/T]ATTATATAACATAAT | 221178 |
rs111216655 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189945 | TATATAATATATTAC[A/G]TAATATATTATATAA | 221178 |
rs111216693 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190032 | TAACATAATGATATA[C/T]AATATATATTATTAT | 221178 |
rs111234977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185676 | AACATCATAATTGAA[A/G]GTTTCTCAATTCCTG | 221178 |
rs111238839 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290900 | GTGAGGGGCATGGGT[A/G]AGGGGCACAGGTGAG | 221178 |
rs111253824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193342 | TGACAAAGGCCAGTG[C/T]TGGAGGAACTGGGAG | 221178 |
rs111255242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189305 | TGAAACCCCGTCTCT[A/G]CTAGAAATACTAAAA | 221178 |
rs111258834 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122572 | GCAGAGCGATGACCT[C/G]TAACAATTTTGTTGC | 221178 |
rs111269169 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211703 | CTCTCCCCAGCCCAC[A/G]GCCAGGATTATCTCA | 221178 |
rs111274899 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114112 | ATATGCAGTGTAGAA[A/G]GACAAGTGTAGACTT | 221178 |
rs111275823 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123541 | CAGCATTTGGTTCTG[C/T]AAGAATCTGGTAACA | 221178 |
rs111278953 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291749 | GTCTTTATTTTTTTA[A/T]TTTTTTATTTTTTTT | 221178 |
rs111280847 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011082 | CTGACTCCTCTGCAA[C/T]CTTGGCTTTGGTTTC | 221178 |
rs111288094 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259666 | AAAACCTCATCAGCT[C/T]AACATTATGATACTT | 221178 |
rs111293114 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004407 | TCTCTCATCCAGGTT[G/T]GATGGACCACAGTAT | 221178 |
rs111323329 | snp | A/G | 0.426047 | 0.177503 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103470 | AGCCTGGGCAACAGA[A/G]CAAGACCCTGTCTCA | 221178 |
rs111330614 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294982 | TATTCTTGGCTTTAA[C/T]GGTACATATACCATT | 221178 |
rs111344541 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139819 | ACGTCTGTAATCCCA[A/G]CACTTTGGGAGGCCA | 221178 |
rs111354148 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212950 | GATAGGCATGTGGCC[A/G]GTGGTTTAGAGGAGC | 221178 |
rs111356450 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127949 | GATGATGTAATGAAC[A/G]AACAGCATTTACAGT | 221178 |
rs111361522 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003964 | AGCATTGTTTTGTAC[A/G]CTTGCTTCATATACA | 221178 |
rs111366427 | in-del | -/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121765 | TCATGACATCCCCTC[-/G]TGTTTCAGATTTCCA | 221178 |
rs111367368 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202680 | CTTGCAAAATACAGA[C/T]GGAAGAGAGTGAGAA | 221178 |
rs111369795 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000640 | TCAGGAAAGGGCAAC[A/G]GGACATGCAGAAGCC | 221178 |
rs111376359 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059251 | GCTGGGATTACAGGT[A/G]TGGCCCACTGCATCC | 221178 |
rs111383213 | snp | A/C | 0.46137 | 0.133501 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019081 | TATATGATTCTTATT[A/C]TTATTATTATTATTT | 221178 |
rs111406842 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194557 | ACAACTTCTGAATCC[A/G]TAACAGTTTGAGGAT | 221178 |
rs111408259 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031450 | GTCCACTTTCCCAGA[A/T]CTTTCCAGATACCAA | 221178 |
rs111418073 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172429 | GTCTAAGAACTCCGT[C/T]GTAGTCCTAGATCCT | 221178 |
rs111422021 | snp | C/T | 0.123798 | 0.215808 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060625 | GCACAGCAAAAGAAA[C/T]TATCAACAGAATGAA | 221178 |
rs111422909 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069925 | ATCTCAGAGGCCAAA[A/G]GAAGGTCCCCAATGT | 221178 |
rs111423419 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146065 | GAGAGCTTTGGCAGC[A/C]AGGAAGAATTTGGAT | 221178 |
rs111435025 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266918 | CTCCTCAGCCTCCCA[A/G]AGTGCTGGGATTATA | 221178 |
rs111438506 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253611 | ATTCCATAAGTCAAT[A/G]TGTAGGATGCACCAA | 221178 |
rs111440874 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114817 | ACAAGCATGCACCAC[C/T]ACGCCTGGCTAATTT | 221178 |
rs111463756 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189299 | ACACAGTGAAACCCC[A/G]TCTCTACTAGAAATA | 221178 |
rs111470696 | in-del | -/A | 0.136506 | 0.222754 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061889 | AAAAAATTAAAAATT[-/A]AAAAAAAAAAAGAAA | 221178 |
rs111499388 | snp | A/G | 0.5 | 0 | missense | SPATA13 | GRCh38.p7 | 13:24297472 | TCCTGTTTGACCACC[A/G]GCTGGTGTCCTGCAA | 221178 |
rs111511297 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290397 | AAGAGACCAGGGTGC[C/T]GAGTTCCAGGGCAGC | 221178 |
rs111522446 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097741 | TGGATCATGTAAGGA[C/G]AGGGACCCCCCAACA | 221178 |
rs111526536 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206874 | TCCAGCCTGGGCAAC[A/G]AGTGAAACTCTGTCT | 221178 |
rs111534108 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102535 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCACAC | 221178 |
rs111540377 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055275 | TTCTCCTTCAGTGTT[A/G]TAGATGTTATGTATT | 221178 |
rs111549343 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052012 | TTTGGCTTCCTCTGC[A/G]TGCACTGAAGCCCTA | 221178 |
rs111551067 | in-del | -/TTTGAACACAG | 0.361894 | 0.223562 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074928 | TTGGCATTTGCCTTA[-/TTTGAACACAG]TTTGAACAGTTGGCT | 221178 |
rs111558434 | in-del | -/TT | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291740 | CTCTCTCTGTCTTTA[-/TT]ATTTTTTTATTTTTT | 221178 |
rs111564789 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194478 | TCCAGCTCTGTGAAA[G/T]AGGAGAAACCAACTA | 221178 |
rs111573023 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287074 | GTATGCTCATTTCTC[C/T]GCCTCTGCTGTCTGC | 221178 |
rs111580246 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152602 | CAGCTCCCACATCCC[C/T]GTCTGTGTGACCAGT | 221178 |
rs111589073 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042569 | CACAAGCGCACATCT[A/G]TGCCCGTGCGCGAAC | 221178 |
rs111594974 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024357 | GATGAATGGATGGAC[A/G]GATGGATGGATGGAT | 221178 |
rs111600473 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117630 | TCTTGTCCCAAAAGG[A/G]GCCTTCCTAAAATAG | 221178 |
rs111618453 | snp | A/G | 0.292266 | 0.246401 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201588 | TGGGATTACAGGTGC[A/G]TGCCACCACACTCAG | 221178 |
rs111625554 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077027 | CCCTGGGTTTCTTAA[C/T]GAGCCAGTTTTCATT | 221178 |
rs111632622 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241693 | TGCCGGGATAATTCA[C/T]CTCCCTTGCAACACA | 221178 |
rs111674550 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173565 | TCCTGTCCTTCACCA[A/T]GAAGCATAATGTTAG | 221178 |
rs111675925 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226526 | ATAATTTTCACTTTA[C/T]AAACACTGAGTAATA | 221178 |
rs111677897 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031693 | GACCTCATATGACCT[A/G]CCCTTGGGGAATTTA | 221178 |
rs111677953 | snp | A/C | 0.0923359 | 0.194016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189366 | ATAGTGCCAGCAACT[A/C]TGGAGGCTGAGGCAG | 221178 |
rs111688035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154135 | CATTTTGAAAAAAAA[A/G]GCTTGGCCGTAGCTA | 221178 |
rs111690369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295091 | TCTGAAGAGTATCTG[C/T]AGTTAATTTATTGCT | 221178 |
rs111699682 | snp | A/T | 0.0923359 | 0.194016 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254470 | CTCTGTAACTTCATT[A/T]TTATTTGGTTGTTAT | 221178 |
rs111703179 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070744 | AGGCCTCAATAGAAC[A/G]GAAGGCTGACCCTCC | 221178 |
rs111707078 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098609 | TAAAAAAAAAAAAAA[C/G]AAGAAGAAGAAAAGA | 221178 |
rs111709727 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181305 | TAAATTTATTGAAAC[-/T]TTTTTTCATAATAAA | 221178 |
rs111713269 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993830 | TTATGCAGGCTGAGG[A/G]TGAGGTCATTGCATA | 221178 |
rs111725063 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997551 | TATTAGTCCATTTTG[C/G]ATTGCTATAGAGAAA | 221178 |
rs111732630 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285568 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGATGTAAT | 221178 |
rs111755000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178800 | TAATTGATATGTAAC[A/G]CATCCATTTAAAGTA | 221178 |
rs111762229 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198115 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTAGCTGG | 221178 |
rs111763992 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121868 | ACCTCCCATCCCCCT[C/T]GATCCCCCAAAATCC | 221178 |
rs111765395 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016004 | GTGACTTGGAGGGTA[A/C]GCGGTGTGTATGTGT | 221178 |
rs111779175 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277180 | CCGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCTA | 221178 |
rs111779272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140654 | GCTTTATTAAGCACA[C/T]GGGACTGCAACTAAT | 221178 |
rs111785428 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055852 | CATTGGCCGAGGAGT[A/C]CAATCCACCACCGCA | 221178 |
rs111788234 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245828 | TCCTGGGCTCAAGCA[A/G]TCCTCCTGCCTGAGC | 221178 |
rs111792172 | in-del | -/T | 0.398894 | 0.200825 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121024 | CTTGCTTTTCTTTTC[-/T]TTTTTTTTCTGAATT | 221178 |
rs111801156 | in-del | -/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116777 | CTACCAGCCCCCCCC[-/G]CCCCAATGTGCTGAT | 221178 |
rs111803671 | snp | C/T | 0.030665 | 0.119967 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303574 | TTCAGTAACTCCGAG[C/T]AGAAATCACATCTTG | 221178 |
rs111805005 | snp | A/C | 0.102726 | 0.202016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049965 | GCACCCTCTGCCTCC[A/C]CGGTTCAAGCAATTC | 221178 |
rs111822567 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077233 | ACGAGAAATAGCCCC[A/G]GTCCTGGCGACAGAG | 221178 |
rs111827015 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154846 | TTTGGAGCTGTGTGA[A/C]TGATAGACCAGTTTT | 221178 |
rs111849271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036122 | ACTAGAAATTAAAAT[A/T]GAGAAGTTTCAAAAA | 221178 |
rs111858292 | snp | C/G | 0.421684 | 0.181726 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997550 | ATATTAGTCCATTTT[C/G]CATTGCTATAGAGAA | 221178 |
rs111871423 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062977 | AAAGTGCCCCTGGGG[G/T]TTTGTGGGGGAGACT | 221178 |
rs111880392 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255203 | CCTGTCCTGAGGACA[C/T]AGTCACCAGGCTGAT | 221178 |
rs111892356 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102068 | TCTATATTTTTTCCA[C/T]AGCAGCTGCACCATT | 221178 |
rs111894474 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156701 | GCCACCAGTTATTGA[A/G]CATTTGACCACGTGC | 221178 |
rs111910584 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119319 | CAGGAAAAAAAAGGG[C/T]ACTTGAGCCATGTTC | 221178 |
rs111916470 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124556 | TCTGGTGAGAATGGC[A/G]GTCCTGGAGGTGAAT | 221178 |
rs111929244 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135692 | GACAGAGCAAGAATC[C/T]GTCTCAAAAAAAAAA | 221178 |
rs111940446 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175168 | TCTAATCCTTTTGGT[C/G]GAGGGCATTAATCCT | 221178 |
rs111940849 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255837 | GTAAGCCCACAAATT[A/G]AGCTCAGCAAACCAG | 221178 |
rs111941012 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277608 | TTCCTATCCTGGTTC[A/G]GACCCAGCCCCTGTA | 221178 |
rs111970685 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140366 | CCCAGCAGACAGAGA[A/G]GATATTTTCAAAATA | 221178 |
rs111971650 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065613 | TCCTCACAAGACAGA[C/G]AGAGACGTCCCCTAA | 221178 |
rs111973132 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036817 | CTGTCAATTTTTATT[C/G]ATTGATTGATTGAGA | 221178 |
rs111976455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214896 | TGGTTTTGAACTTCT[C/T]GCAAAAGTCAGAATA | 221178 |
rs111993536 | in-del | -/CACACA | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201032 | ATTCAGCTAGTCAGT[-/CACACA]CACACACACACACAC | 221178 |
rs112006626 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303211 | AGGATGCCGTCAAGA[C/T]GGGGTTGACACAATG | 221178 |
rs112009068 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092732 | CACATTTGGCAGCTT[C/G]CTATTTCTACATGTT | 221178 |
rs112009883 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300347 | TGATACAAGTTTTGC[C/T]CTGAAACATGTCCAC | 221178 |
rs112012446 | snp | C/T | 0.105569 | 0.204058 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096491 | GTAATCCAAGCTACT[C/T]GGGAGGCTGAGGCAG | 221178 |
rs112016402 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060398 | GAAGGAGACTGAAGT[G/T]GGATCCCTTCCTTAC | 221178 |
rs112042441 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235563 | TCAGGAGCTCGAGAC[C/T]AGCCTGGACAGCATA | 221178 |
rs112045343 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130215 | ACAAGCCCCTGCACC[C/T]GGGAGTCCACCCTGG | 221178 |
rs112046903 | in-del | -/AAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212297 | GAGACCCTGTTTAAG[-/AAA]AAAAAAAAAAAAAAG | 221178 |
rs112047751 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304850 | GCATGTGTGGGGGTG[C/T]GTGTGTGTATGTTTC | 221178 |
rs112067538 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157980 | TAAGAAAATGATGAA[A/T]GTAAACAACGTGGCA | 221178 |
rs112088108 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202922 | AAACAGGAAAACCCT[A/G]ACTTAGGAAACAGTA | 221178 |
rs112096187 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989249 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 221178 |
rs112096528 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198240 | CCTTGTGATCTGCCC[C/T]CCTTGGCCTCCCAAA | 221178 |
rs112098521 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093329 | AAATTCCTTTTCCAG[G/T]CACCAGTATCCCACT | 221178 |
rs112118142 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184711 | CATGATCTCAGTTGT[C/G]AAGGTCCAAGTGACT | 221178 |
rs112128176 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160194 | CGGAGATGAGACTCC[G/T]CTTCCCGCCCTGGGG | 221178 |
rs112132770 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197005 | GAAAAGAGGAACTTA[C/G]TTCTGTAGAAATCTT | 221178 |
rs112145609 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024213 | GAACTGGCCCCATCC[A/G]CATCCACAGTTTCCT | 221178 |
rs112160545 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000040 | TGCCCTCATTAGTTA[C/T]CACCAATATGCATAT | 221178 |
rs112168010 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245038 | CGTGGGAGAGGGCAG[A/G]TCTCTATGATGGTGT | 221178 |
rs112169517 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256533 | ACAACTAAATTTTTC[C/T]CAAAATATAGAAAAT | 221178 |
rs112172290 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286587 | TGCTCGGTGTTTCTC[A/T]GTGGTCCTCGTGCCT | 221178 |
rs112173202 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287458 | GTGAGCCAGTGTGCC[C/T]GGCCCCTCTCTTAAG | 221178 |
rs112175596 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066857 | GATTCAGAGACTCCG[G/T]CCAGATCTGGCAGAC | 221178 |
rs112181291 | snp | A/G | 0.290977 | 0.246619 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206461 | GCTTTTACACTGTTG[A/G]TGGGAGTATAAATTA | 221178 |
rs112201673 | in-del | -/TG | 0.0991586 | 0.199366 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281618 | GGAAAGGAGGTGATG[-/TG]GTGGCTGGGATGTCG | 221178 |
rs112212602 | snp | A/G | 0.188631 | 0.242351 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173237 | CATGTGTCACCAGGC[A/G]TGGCTAATTTTTTGT | 221178 |
rs112216173 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101364 | CACTGTTGTACTTGA[-/T]TTTTTTTTCATGGTT | 221178 |
rs112221936 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116456 | CAGCAGGTGGGGATC[G/T]TGGGGGCATCTTGGA | 221178 |
rs112225306 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206288 | CACTAAAGAAGACAC[A/G]TGTGGCCACAAAACA | 221178 |
rs112244794 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123687 | ATATATTCGTAAGGG[C/T]CTTCTTGCCAAAGTT | 221178 |
rs112252232 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098072 | CCCTAGAAGGCTATT[A/G]AAGACCAGGCCCCAG | 221178 |
rs112269155 | snp | A/G | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978885 | ATTTTTTTTTTTGGT[A/G]GAGATGGCGGTCTTG | 221178 |
rs112274389 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226922 | AGAGAAGTGAGACTG[C/T]ATATTGTCTGTTACC | 221178 |
rs112302987 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021410 | AGTCAGGAGGATCAC[C/T]TGAGCCCAGGAGTTT | 221178 |
rs112306621 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022006 | GTGAGCCACTGCGCC[C/T]GGCCAGTTGTTGGAA | 221178 |
rs112314381 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142624 | TTAAGAGGTAATTAC[C/T]ACTCTTCAACAACTT | 221178 |
rs112318810 | in-del | -/GAG | 0.127944 | 0.218179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188782 | ATTTTTCTAGCTAGA[-/GAG]GAGAAGTCAGTGTCT | 221178 |
rs112321813 | snp | C/T | 0.317933 | 0.240593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027323 | TATTTTTAGTAGAGA[C/T]GGCGTTTCACCATGT | 221178 |
rs112323997 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126644 | TCACTGCAGCCTAGA[C/G]CTCCTGGGCTCAAGG | 221178 |
rs112328310 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997857 | GGATCCACCCTCATG[A/G]GCCAAACACTTCCCA | 221178 |
rs112332205 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014070 | TGAGTGGCTTTGACA[A/G]CAGAAATGGTTTGCC | 221178 |
rs112333119 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209167 | ACTGTACTCAGGACA[A/G]GCCGATTTCAGGAAT | 221178 |
rs112334197 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001126 | GAGTGGCCTCTTCTA[C/T]TCTCACCCCCTACTC | 221178 |
rs112344847 | in-del | -/G | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141168 | GCAGAGTGAGACTCT[-/G]GGCTCAAAAAAAAAA | 221178 |
rs112348330 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256690 | CTCTGGCCCTGTTTG[G/T]AGCACCTGTCTTACC | 221178 |
rs112406229 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173651 | CTGTCTCTCTAAAAA[A/G]GTTTTAAACTGTGAA | 221178 |
rs112408490 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115497 | ATGCGAAGGATGTAC[A/G]TTGCGTGCTCCTTAT | 221178 |
rs112416760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209836 | AGTTTTCTGAGGCGC[C/T]TCCATGCTGTTTTCC | 221178 |
rs112421492 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038710 | CAAACAACTCTATTT[A/T]CAGAAACAAGCAGGG | 221178 |
rs112421933 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285701 | TTTTTTTTTTTTTGA[C/G]ACAGAGTTTTGCTCT | 221178 |
rs112450702 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180868 | CTGATAAATGCATTG[C/G]TAGGCAATTTCATCT | 221178 |
rs112455495 | in-del | -/GTTTT | 0.252421 | 0.249988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105113 | TGGCTTCTTACAATC[-/GTTTT]GTTTTGTTTTGTTTT | 221178 |
rs112455758 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056460 | CATATGATGGATTAG[A/T]TGCTCACCTTACATG | 221178 |
rs112459374 | in-del | -/CTTTA | 0.368119 | 0.220336 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232364 | TTGAGGGCAAGTCTT[-/CTTTA]CTTTACTGATTACTG | 221178 |
rs112463694 | in-del | -/GTGTGTGTGT | 0.5 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979285 | GAAGTGTGTGTGTGA[-/GTGTGTGTGT]GTGTGTGTGTGTGTC | 221178 |
rs112485647 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237129 | TTCTGAGGCCGAGGT[C/G]GGTGAATCATGAGGT | 221178 |
rs112486237 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134290 | GGCTTTTCCAAGTAC[C/T]CTAAAACCACACCAT | 221178 |
rs112490596 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196868 | AGATAAGGAGAAGCA[C/T]GATTTCTAACACTCT | 221178 |
rs112491069 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143950 | GTGGTTGCCCTGAAA[C/T]CACAGGGCATATGAT | 221178 |
rs112497927 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084544 | TTTCTGGTTTTTCTT[A/T]AAAAAAAGCAACACT | 221178 |
rs112517321 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993783 | AACTCCCCATCCAGC[A/T]GTAAACCACCCCTGC | 221178 |
rs112524130 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156000 | CCACCTGTGTTGCAG[C/T]GTGTGTCGGAATTTT | 221178 |
rs112529040 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173683 | AATGGGTGTTGAATT[G/T]CATCAAATGCTTTTT | 221178 |
rs112531922 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181558 | CTTTTTTGTTAAAAA[C/T]GAAGACAGAAACGTA | 221178 |
rs112535708 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179542 | ATTCATTGTTATGCA[A/G]CCAATCTCCAGAATC | 221178 |
rs112537229 | in-del | -/T | 0.339882 | 0.233284 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029364 | ACATTTTAGCTTACA[-/T]TTTTTTAGACAAATA | 221178 |
rs112544106 | in-del | -/GAAGGGGAA | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203327 | GACGGTAATTTAGGG[-/GAAGGGGAA]GAAGGGGAAGAAATA | 221178 |
rs112545598 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029991 | TAGTATTCCATGGGA[A/T]TTCATAGCAAAATTG | 221178 |
rs112552073 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155144 | TGAGCCACCTTGCCC[A/G]GTTGGTTATTATTAT | 221178 |
rs112561945 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160682 | GCCGGGCTGGGGGCG[C/T]GGCCTGGTGGGGAGC | 221178 |
rs112579360 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24137125 | GTGAGCCACCGCGCC[C/G]GGCCTGTTCTTTATT | 221178 |
rs112587412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208006 | CCTCATGTGTAATTA[A/G]GAGTAATTTAGGGAA | 221178 |
rs112591644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983295 | TTACTGCGTCTTCAC[A/G]TGGTCATCCTTCTAT | 221178 |
rs112594358 | in-del | -/A | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119307 | TGTGGTGGGCCCAGG[-/A]AAAAAAAAGGGTACT | 221178 |
rs112604340 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160950 | AAGACGGCTTCGGGC[G/T]CGCGGCTCTGCCGGG | 221178 |
rs112612236 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214810 | TCATCTTGCATCTCC[A/G]CTTTCCTTTTTGAGA | 221178 |
rs112616273 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192361 | GTGTTTTGAGGTGTT[C/T]GTCTCCTCCTCCTTG | 221178 |
rs112623675 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140515 | AAACACAAGGGTCAC[A/G]TGCAGAAGCAGAGCT | 221178 |
rs112626969 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026872 | CTCCCAAAGTGTTGG[G/T]ATTACAGGCGTGAGC | 221178 |
rs112655486 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030063 | ACACACACACACACA[C/T]ACGCACACACACACA | 221178 |
rs112656200 | in-del | -/GTGT | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197991 | CTCCCCTGTTACCTC[-/GTGT]GTGTTTGTTTGTTTG | 221178 |
rs112669132 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116594 | GGAGTTCATTTTACC[C/T]TCATTTTACAGATGA | 221178 |
rs112681660 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112554 | TCTTGTGCCAGGCAT[A/G]CACACACACACACAC | 221178 |
rs112690375 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990587 | GTCTTGCCCAACACT[-/C]CCCCAGCCTGGTTTA | 221178 |
rs112694222 | in-del | -/TGTT | 0.113685 | 0.209567 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148915 | CATGGTTTCCATGAG[-/TGTT]TGTTTATACCAGGAA | 221178 |
rs112730047 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133062 | GACAGTTGAGGCCAG[C/G]GAAGGAGCCAACATT | 221178 |
rs112731903 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156828 | TTCCTAGAACCCACA[A/T]GGACAGAGAGCAGAA | 221178 |
rs112768628 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103903 | GAAAATCTTAAAGGG[A/G]GTGTCCTCACACCAG | 221178 |
rs112773489 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261735 | TGTAGAGAGAAAAAT[A/G]CCCACTGGATCCAGT | 221178 |
rs112781865 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236800 | TGGTGGGAAAATAAA[A/G]TGATGGTACGGCTGC | 221178 |
rs112782391 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145904 | GATGGAGGGAAGGAG[C/T]CTATTCCATATGTGA | 221178 |
rs112790881 | in-del | -/TCCC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278971 | CCTTCCTTCCCTCCT[-/TCCC]TCCCTCCCTCCCTCC | 221178 |
rs112793419 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065149 | GTTTACCTGTCAGGG[A/G]GATGTCTAATAATGC | 221178 |
rs112820528 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219167 | CTTGCTACAAAACCA[C/T]TAATTGAATTGCAAC | 221178 |
rs112851255 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192813 | AGAGGGTGACATGGG[A/G]AAAAAAGGCCTTCTG | 221178 |
rs112851672 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193314 | GAAAGTAGGTGAGGG[C/G/T]GGGGGAGAGAGATGA | 221178 |
rs112867560 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277194 | TTACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 221178 |
rs112869131 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020091 | GCACCAAGCCTCACC[A/G]ACAGCCAGACTTAAC | 221178 |
rs112877296 | snp | C/G | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207206 | GGAACAACACACGGT[C/G]GGGTCTGTCTGAGGG | 221178 |
rs112881206 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291914 | GGCGCCCGCCACCGC[A/G]CCCGGCTAATTTTTT | 221178 |
rs112907350 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206479 | GGAGTATAAATTAGT[A/T]CAGCCCTTGTGGAAA | 221178 |
rs112928625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214666 | GAGGGATGCTCCCTG[C/G]TGTTGTCCAGTCATC | 221178 |
rs112931737 | snp | A/G | 0.32 | 0.24 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137052 | AGCCGGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 221178 |
rs112938457 | in-del | -/GGTG | 0.0108647 | 0.0728993 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103348 | GTATAGGCTGGGTGC[-/GGTG]GGTGGCTTGCACCTT | 221178 |
rs112941345 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169832 | CCACTCTCCTCTCCT[A/G]CCTGGCTGCTCTGCC | 221178 |
rs112943279 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026551 | GTAGGAATTGGATAC[-/A]AAACTGCTGTTTATT | 221178 |
rs112945942 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23979954 | TCTACATATTGTCAC[C/T]TCGCCCGCACTTTTG | 221178 |
rs112951070 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284794 | ATCAGTGTTCGGCCA[A/G]TGCTTTCCACTTGAT | 221178 |
rs112952621 | in-del | -/TGTCCTC | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042126 | GCTGAGAAAGCGCGG[-/TGTCCTC]TGTCCTCTGTGTCAC | 221178 |
rs112953274 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148864 | TAAGGACACAGGAGC[G/T]GCTGTTCATTCTGGT | 221178 |
rs112977230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250124 | TGAGATTCTAACCAG[A/G]GAAAGGTAGCAGGGC | 221178 |
rs112979790 | snp | A/G | 0.427575 | 0.175975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198089 | CAACCTCCACCTCCC[A/G]GATTCAAGCGATTCT | 221178 |
rs112986495 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232226 | TGGAGTCCGAAGGCC[C/G]AAGAACCAGGAGCTT | 221178 |
rs112986785 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028311 | GAGGATATCTTGTTG[C/G]TATACTGCTCCCAAC | 221178 |
rs112996898 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092164 | GGTTTAGGGAGGTAC[C/T]TATTCTTCTATTCTG | 221178 |
rs113000256 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268353 | ACAGTATCGAGGAGT[A/C]TTTTGAGCCTATAAT | 221178 |
rs113005229 | in-del | -/AAC | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138315 | GTCTGAAAAAAAAAA[-/AAC]AAAAAACAGTTTTAC | 221178 |
rs113023159 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147754 | AAACATTAACTCCCC[A/G]TTCCCTCCACACCCC | 221178 |
rs113030555 | snp | C/T | 0.317933 | 0.240593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024961 | ATATATATATAAATA[C/T]ATATATAAACACAGA | 221178 |
rs113035097 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138227 | CAAGAGAATTGCTTG[A/C]ACCCAGAAGGCAGAG | 221178 |
rs113037522 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297174 | CTCCTAAGTAGCTAG[A/G]ACTACAGGTGTGTGC | 221178 |
rs113043645 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978871 | AACTAATTAAAAAAA[-/T]TTTTTTTTTTGGTAG | 221178 |
rs113065472 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285475 | CTAAGTGAGCAGCTA[A/G]TACTTTTTTAAAAAG | 221178 |
rs113068079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209860 | GTTTTCCACAGGGGC[C/T]GTACTAATTCACAAT | 221178 |
rs113091837 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120893 | CAAAGGTGAACTCAG[A/G]TACTGCGCTGTCACG | 221178 |
rs113103405 | snp | C/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039605 | TGGGCCTCGAGGGGT[C/G]GTTTCTTAGTTCTTG | 221178 |
rs113117785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139757 | CTTAATTGATGTACC[A/T]GTTTTTGTTTTAAAA | 221178 |
rs113127899 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103285 | CTAGTCTTTACACAC[C/T]TATAATTTGAAAATG | 221178 |
rs113136941 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116231 | CTGCTTTTCATGGAT[G/T]GCATCTTCTCACTGT | 221178 |
rs113189134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105739 | TCCCCAGTACCTCCA[C/T]ATGTGACTGTATTTG | 221178 |
rs113190502 | snp | A/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045471 | TCAAATGCCCTAAAC[A/T]AGCTAAGATTATTAA | 221178 |
rs113193425 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039579 | TCTTTCTCACTCTCA[A/G]TAGGAATTCTTGGGC | 221178 |
rs113206133 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203161 | ACAGGCCCCAGTGTG[C/T]GTTGTTCCCCTCCAT | 221178 |
rs113208653 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149757 | AAAGGCCCTGCGGGG[C/T]GGATAGAGCTGGAGA | 221178 |
rs113219968 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132882 | AGTATGATGAGGGCA[C/T]GAGAATCACTTGAAC | 221178 |
rs113229168 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054670 | AAATATGTGAAATAT[A/G]ATAATAGTAGCGCAC | 221178 |
rs113231727 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082853 | AAAAAAAAAAAAAAA[A/C]ATAAGATCTTTGCAT | 221178 |
rs113237699 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045121 | CCTATGTATAATTTA[A/T]ATCACTCATTGCCAA | 221178 |
rs113247828 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118516 | GCTCATTCATTCCAA[-/G]CTTGTAGCCTGCATC | 221178 |
rs113250728 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080353 | GGGCTGTGAAGAGAA[C/T]AAGCAGGAACCAACG | 221178 |
rs113258532 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160219 | CTGGGGGGTGGGGGC[A/T]GGCTGGTGGCTGAGG | 221178 |
rs113259408 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165704 | GGCAGGAGGCTGGCA[A/G]TGAGATGTGTTGTGG | 221178 |
rs113273742 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076383 | TAAATCAATGGGAAA[A/G]CACATCTGCAACTGG | 221178 |
rs113286683 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289347 | CATATAAACAAAATC[C/T]GTATAGTTAATCTTG | 221178 |
rs113287074 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992073 | CACAAAACCTAGGAA[G/T]TGAGTTAGAATAGTG | 221178 |
rs113313052 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143872 | CTCTGGCCAGATGAC[C/T]TTAGCCAAGTTATTC | 221178 |
rs113320199 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289466 | TTCTAAGGGTTATGC[C/T]ATAAGAACTATGGAG | 221178 |
rs113345862 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103905 | AAATCTTAAAGGGAG[C/T]GTCCTCACACCAGCG | 221178 |
rs113347020 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989942 | ACCAGACATTGAATC[C/T]GTGGATACTTTGATC | 221178 |
rs113350811 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111587 | TAACTTGTATTTTTT[A/G]TAGAGATGGGTTTTC | 221178 |
rs113367480 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260500 | AAGCCTGTTTATGGC[A/G]GTTGCTTTATTATGA | 221178 |
rs113375108 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987224 | GGTTTTCTTTCAGTG[G/T]TTGTGTCTCTATTTA | 221178 |
rs113376190 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111709 | CCATGCCCGGCCTGC[A/G]TCCATATTTTAATGT | 221178 |
rs113384106 | in-del | -/CTCGTGCCTCAGCCTC | 0.0551013 | 0.156571 | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035262 | CACATTCAGGCAATT[-/CTCGTGCCTCAGCCTC]CCGAGTAGCTGGGAT | 221178 |
rs113387088 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212923 | CTCACCATGTGGTAG[A/C]TGTACCATGAGGATA | 221178 |
rs113395063 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133893 | AGAAGAAGTGACAGC[C/G]TGCGTAGAATCAGAC | 221178 |
rs113403554 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110664 | TAGATCCTGCGGACA[C/T]AGAAAGGAAACAAAC | 221178 |
rs113412397 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049694 | AACACGAAACTGATG[A/G]GCTGTGAAGGGAGTG | 221178 |
rs113438094 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072898 | TCTCATCCAAAACTA[A/T]ACCTAATGCACAGAT | 221178 |
rs113440923 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226427 | CTTATTTTAGAGTAG[A/G]TCATAAGCACCTCAT | 221178 |
rs113450726 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026821 | TGACCTCGTGATCCG[A/C]CCTTGTGATCCTGAC | 221178 |
rs113474651 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108662 | TGCTTTTCATGGTAG[A/G]GGGGGGGAAGCCTGA | 221178 |
rs113482773 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166091 | TAGGGATTTATGTGG[A/T]TTTGCAGATTCTGCT | 221178 |
rs113500048 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022329 | GGCGTGAGCCACTGC[A/G]CCTGGCGAAAAATCT | 221178 |
rs113512680 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121445 | GCAGGCTTGTTTCAA[C/T]ATGAAAGTGCCAATT | 221178 |
rs113517036 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255894 | TTGGGGAGATTTTCA[A/G]ATGAACTGAATATTT | 221178 |
rs113541471 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048465 | AGTAGATCTAGTAAA[C/G]TAATCAAGGATGAAG | 221178 |
rs113546035 | snp | A/T | 0.251578 | 0.249995 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060217 | CCAAAACAGCATGGT[A/T]CTGGTACAAAAACAG | 221178 |
rs113547778 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091024 | CGAAGTCTCTGCTTA[A/G]TTAGCCTAGTGGTTG | 221178 |
rs113550673 | snp | A/G/T | 0.0341968 | 0.126537 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236791 | GTGCATTGCTGGTGG[A/G/T]AAAATAAAATGATGG | 221178 |
rs113561904 | snp | A/C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098606 | TCTTAAAAAAAAAAA[A/C/G]AAGAAGAAGAAGAAA | 221178 |
rs113562662 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190265 | ATATAATATACATAA[A/T]ATATATTATTATATA | 221178 |
rs113563798 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110583 | GCAGGGTTTGTGGGT[A/G]AATAACCATTTGTTA | 221178 |
rs113565842 | in-del | -/AGAG | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065610 | AGCTCCTCACAAGAC[-/AGAG]AGAGACGTCCCCTAA | 221178 |
rs113565933 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126527 | AATAAGCATTTACGT[A/G]TATATATTTGTGTGT | 221178 |
rs113587090 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979161 | GGATATAATTATATC[A/T]TCTTCCAGTCATGAT | 221178 |
rs113591985 | snp | A/T | 0.0067877 | 0.05786 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168849 | ATTTTAATTTTAAAA[A/T]TTTGAAGTTAAATAA | 221178 |
rs113593664 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112555 | CTTGTGCCAGGCATA[C/T]ACACACACACACACA | 221178 |
rs113632702 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066856 | AGATTCAGAGACTCC[G/T]GCCAGATCTGGCAGA | 221178 |
rs113639307 | snp | C/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041089 | GCCTGCCTGTGCTCT[C/T]ATCTATAGGAACATT | 221178 |
rs113679988 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122427 | TTCCGCATCATCTTC[G/T]TACCAGTCTTCATCG | 221178 |
rs113684695 | in-del | -/CCTCGTGATCCGC | 0.398354 | 0.201224 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026809 | GTCTGGATCTCCTGA[-/CCTCGTGATCCGC]CCTTGTGATCCTGAC | 221178 |
rs113687854 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077442 | ACACACGGACATAAA[A/G]ATGGAAATAATAGAT | 221178 |
rs113722488 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139514 | GGAGAATCTTTGTAG[A/G]TTTATTACCATCTGT | 221178 |
rs113722580 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202028 | TCTTTTTCTGGCTTA[A/G]TAGCTCATTTCTCCA | 221178 |
rs113723819 | snp | C/T | 0.5 | 0 | missense | SPATA13 | GRCh38.p7 | 13:24297676 | AACAAGAAGACAAGG[C/T]GAGGTGGCTGCAGGC | 221178 |
rs113723930 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155631 | AATCCCAATGGCTTT[C/G]TGCAGATTCTGGCCT | 221178 |
rs113726274 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158928 | TCATCTGAGGGCCAG[A/G]CCTGTTTCCCAAGGA | 221178 |
rs113727526 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025192 | TATTTTCCTATTTTT[A/G/T]TTTATTTCCTAAAAT | 221178 |
rs113744758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013990 | TGGAGTGTGCTAGAG[G/T]CAGAGCCTCCAAACC | 221178 |
rs113767563 | in-del | -/A | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242049 | GAGTGAGACTGTCTC[-/A]AAAAAAAAAAATGAA | 221178 |
rs113782121 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022316 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCGCC | 221178 |
rs113789750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110109 | AACTACATCACTCCA[A/G]CTATAGGGTAAATAA | 221178 |
rs113793313 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202523 | TTCTTTCTTTCCCTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs113793444 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119058 | CTGCAGGCGCCTGCC[A/G]CCGCTCCCTGCTAAT | 221178 |
rs113795322 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121924 | TTGCATGATCGGGTC[A/C]CATCTCCTGGGGTTG | 221178 |
rs113803486 | in-del | -/T | 0.078151 | 0.181571 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195245 | TTTACTTAGATAATA[-/T]TTTTCAGTGTGCATT | 221178 |
rs113818277 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104367 | GAAAAAGCAATTTAG[C/T]CCACTCAATTTTTAG | 221178 |
rs113835456 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104251 | TAAAGCTAGAATGGG[-/T]TTTTTTTTTTTGTTT | 221178 |
rs113837138 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183540 | CACATGCAGCCCAAG[A/G]TGGCTTTGAATGGGG | 221178 |
rs113838398 | in-del | -/ACTT | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130997 | GCTTCATCGTGATTC[-/ACTT]ACTTGCCTTCGTGTG | 221178 |
rs113841110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150017 | GGGGCATGGGAGAGT[C/T]GGGGGACTGTCCCAC | 221178 |
rs113852955 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089577 | GTTGTGGTAGAATTT[A/G]CATAGTATAAATGTA | 221178 |
rs113869208 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069976 | TTCCTATCTGAGATG[C/T]GGGAGTGCGGTAGAG | 221178 |
rs113883995 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221542 | TGGGGTTGAAGGGTT[G/T]GGACACAGATGTGCA | 221178 |
rs113885667 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091740 | CGCTTGAACCTGGGA[A/G]GCGGAGGCTGCAGTG | 221178 |
rs113898401 | snp | A/G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112706 | TCTCAGTCTTCATCT[A/G/T]CTTTCTCAGTCTTGA | 221178 |
rs113900724 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130632 | AATAACTCCATGTCC[A/G]TGTTCCCTAAGTGAA | 221178 |
rs113905293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112354 | CCTACAGCACCTTCT[G/T]TGCCACTCTGTAGTG | 221178 |
rs113912894 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205602 | TAAAATTCATGTGGA[C/T]CAAAAAAGAGCCTGA | 221178 |
rs113931192 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190232 | ATATATAATATATAT[C/T]ATTATATAACATATC | 221178 |
rs113931844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109127 | CCCGCACCCCACAAC[A/G]GGCCCTGATGTGTGA | 221178 |
rs113940956 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181079 | AGGTACAGAAAAATA[C/T]GGTATAAAAGTTTTT | 221178 |
rs113943373 | snp | G/T | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031128 | TTAGTTGTGGCTGAT[G/T]TATTCATTGATTGAT | 221178 |
rs113944965 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029717 | ACAGATTATTTCATC[A/G]CCCAGGTATTAAAGC | 221178 |
rs113948715 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982529 | CTAATACTTTTATAG[A/C/G]TACTATCCTGAGTCA | 221178 |
rs113951160 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244647 | GGCAGGTGAATTGCT[C/T]GAGCCCAGGAGTTTG | 221178 |
rs113985883 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112970 | AGACTCAACAGGAGG[A/G]GCTACTTACTGTAAT | 221178 |
rs113987228 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112451 | TACACTGTGCTTTGT[G/T]CATCCTTGTACTTCC | 221178 |
rs113990315 | in-del | -/TGTGTG | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987002 | GTGAATGGATATATC[-/TGTGTG]TGTGTGTGTGTGTGT | 221178 |
rs113998475 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205477 | ATGCTATGGATAGGA[A/G]GAATCAATATCATAA | 221178 |
rs114014753 | snp | C/G | 0.0217236 | 0.101931 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252739 | CAAAACCTAACTCTG[C/G]CTGTCTTAAGCAAAA | 221178 |
rs114033112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078960 | GAAAAACAGACAACT[C/G]TATCATCACCCAATA | 221178 |
rs114039620 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109804 | TTTTACTCTGGTAAA[A/T]ACATCTGCAATGAAT | 221178 |
rs114057902 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281275 | TTGGTCTCTTAGACA[A/G]CTCACTTTCACTTTT | 221178 |
rs114075799 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043882 | CCCTCAAAATAAGGA[C/T]TGCCAGGGGAGGGGT | 221178 |
rs114081949 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185044 | CGTGTATCGAGCATT[G/T]TGTTTTGCTTCTCCA | 221178 |
rs114091484 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172528 | CATTCAAGTTAATTT[C/T]TGTAGCAGGCATGAG | 221178 |
rs114108766 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289295 | CTAGATGAATCTTCC[A/G]TAGAAAGGAGATGTT | 221178 |
rs114134558 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100952 | TTAGGGCATTGAAAA[G/T]GGAAAGAAAAACTTC | 221178 |
rs114147252 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998679 | GTTTTTCTTCTATGT[G/T]TTCTTACAGAAGTTT | 221178 |
rs114149634 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127238 | CCAGGCTGGTAGCAG[C/T]GAGGCCACCCTCTCC | 221178 |
rs114158613 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197867 | TCTCAGTGGGCATGG[A/G]GTTTCCTGGAGGCTG | 221178 |
rs114189516 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292768 | TTTGGGAGGCCGAAA[C/T]GGGTGGATCACATGA | 221178 |
rs114189864 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984877 | CAGCTTTGAACATGA[A/T]TGCAAGTCCCTGCAA | 221178 |
rs114200057 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031502 | ATGACTAGACATATG[C/G]TTGGCAGGAATTACT | 221178 |
rs114201334 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192018 | ACACGGCAAAGTGAG[A/G]TGGAGTCCTGCTAAC | 221178 |
rs114201747 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051005 | GTTTTTGCAGGTGAG[C/T]GTACTGTGAGCTAAG | 221178 |
rs114213475 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028471 | ACTCCCTTGGTTGCA[A/G]TTGTGATGTCAGCTG | 221178 |
rs114258825 | snp | A/C | 0.117537 | 0.212022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272087 | GAGGAAGCGGACGTG[A/C]GGGTGCTCCCTCCCA | 221178 |
rs114304591 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238720 | CTCACTCCTTAATGT[A/G]TATGTTTTTCACGTT | 221178 |
rs114317750 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181415 | CTTAAAACACAAATA[C/T]ATTATACAGCTGTAC | 221178 |
rs114321066 | snp | C/T | 0.000591821 | 0.0171919 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224698 | CCTCTGCTGACCTTG[C/T]TGCCCTTACAGTATT | 221178 |
rs114323817 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049108 | CTAACCCTGGACATG[A/G]TGAGGAGCCTAGAAC | 221178 |
rs114328981 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988292 | TTCCATAATGTGTAT[A/G]TACCACATTTTGTTT | 221178 |
rs114331059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084158 | TCCTAATTATCTTCC[A/G]TAACTTAGCAACAAG | 221178 |
rs114332393 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251270 | GTGGGGAGGAGTAAA[G/T]GAGGCTGAAGAAGGA | 221178 |
rs114336008 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260283 | CAAAAAGTGGAGGCC[A/G]GAGAAAGGAGAGCAC | 221178 |
rs114355176 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094555 | TAGACCTTATTCTTT[C/G]TTTATGCTTAAAATG | 221178 |
rs114359440 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007484 | CTTTAGAGGTGCAGT[C/T]TCCCTCTGTCAGCCC | 221178 |
rs114364470 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013397 | TCCCTCCTGGTTTGT[C/T]CCAGCTCTGGGGCCC | 221178 |
rs114375490 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118246 | CAGAGCACTCACTCC[C/T]CATCATGGTCTCTTT | 221178 |
rs114416354 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307130 | GTGGAGAGCTGGGTG[C/T]GGGGGCTTCTGGGAT | 221178 |
rs114420335 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995495 | AATAACAGAGGTCAG[A/G]TCTGGCAGGGGCCCT | 221178 |
rs114434037 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008809 | CTGATGGCTCTCAGG[C/G]CTATCTTCTGCAGCT | 221178 |
rs114456372 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205694 | AACTATACTACAGGG[C/T]GACAGTAACCAAAAT | 221178 |
rs114459510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235313 | AAATGACTTTTGTCA[A/G]TGCAAACTTTGAGAT | 221178 |
rs114473675 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050177 | GCCAGGCCTTTCAGA[C/T]TCTTTCTGAACCATC | 221178 |
rs114474726 | snp | C/T | 0.00488379 | 0.0491736 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290633 | CAGAAGCTGACGAAG[C/T]TGTACTTTTCCTTCC | 221178 |
rs114475516 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062697 | ACCTGAGCTGTACTG[A/C]ATAAGGGGTTGTGTG | 221178 |
rs114507723 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042045 | GCACAGAGGCAGCCA[C/T]GTGTGTCACATTTCA | 221178 |
rs114517235 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129013 | AAACTCTACACCGGG[A/G]TAAGTGACCCTTTCT | 221178 |
rs114525243 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153077 | CATGTCTACTTAGGA[C/T]CTCTGAGTTGGGACT | 221178 |
rs114525993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196173 | TTCATATGTTACCCA[A/G]ATTTGATGAGGAGTA | 221178 |
rs114526767 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181689 | ACGCATAGAGCTGTC[A/G]TCTGCTATAATAATA | 221178 |
rs114546759 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140863 | CCTGTTTCATATAAT[C/T]GTAAAGGAGAATATT | 221178 |
rs114547254 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051808 | AGCCTGCTAAGAGTT[A/G]TGTTCTCCAGGGCAG | 221178 |
rs114547613 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040174 | AACCAAATGGCGAGT[A/G]CCCTATGCCAGCAAA | 221178 |
rs114557707 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289885 | ACCACACCTTCACTT[C/T]CTGGGTGCTGGGCTC | 221178 |
rs114558327 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047727 | CTTTTTCACTTGTAT[C/T]AGCAAGGGCTCTCCA | 221178 |
rs114566123 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241439 | GACGGCATTACTCAG[C/T]GAAACGCAGAGTGTT | 221178 |
rs114577951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024394 | ATGGATAGATGGAAT[A/G]AAGGAATGATGAACC | 221178 |
rs114590794 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054314 | TCCATCTGCAGCCAT[C/T]TTAGATAGATGAATG | 221178 |
rs114601079 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107346 | GGCACAGTGGAAACT[A/G]TCCCCAGAGAAACGA | 221178 |
rs114608166 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149439 | ATTTTGCCTGTCTTC[C/T]GTTCCTGGACCTTCC | 221178 |
rs114610220 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284822 | GATAAAGAATACCCT[A/C]CCCTCCACTATCTCA | 221178 |
rs114611074 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150194 | CTCTACAGTGCCCGT[C/T]TCCCGTGCTCTCCTC | 221178 |
rs114619780 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303570 | CGCCTTCAGTAACTC[C/T]GAGCAGAAATCACAT | 221178 |
rs114638803 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106515 | CACTTCAGTTGAGCA[C/G]TTGTGCAGCAGTGGC | 221178 |
rs114663950 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032518 | GATTTCATAAGGAGT[A/C]GTTACAAATATGTTG | 221178 |
rs114681973 | snp | A/G/T | 0.0174464 | 0.0919885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054037 | ACAGCTCTGCCCTGC[A/G/T]GGGACACTCTGAAGA | 221178 |
rs114707503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171273 | CCTCATGTGTTCAGC[A/G]CTGTCATTTTTCAAG | 221178 |
rs114712191 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147602 | GCCACCCACACCTTT[A/T]AAAAAAACTTGTAGT | 221178 |
rs114715941 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24122650 | ACATACTGTATATCA[C/T]TTCAAGATACTTGGT | 221178 |
rs114762227 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001722 | TGATGGCCGTGGATA[C/T]GGAGGGAAATGAAGA | 221178 |
rs114778684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249940 | CTGCTTTTTCTCTCC[C/T]GTTCTCAAGGGCGGC | 221178 |
rs114812796 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085660 | CACTTCCATGTGGCC[C/T]GACTCCCTTTCCAGG | 221178 |
rs114817639 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260147 | ACGCTGAGTAGAAAC[A/G]GGGAGCATGTCAGTC | 221178 |
rs114819065 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034395 | CATCAAACTGGTTGG[A/G]TCCAATCACTTAATG | 221178 |
rs114828277 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212201 | GAGGATTGCTTGAGG[C/T]CAGGAGTTCAGGGCT | 221178 |
rs114834354 | snp | A/G | 0.127944 | 0.218179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228030 | CCGCCTCAGCCTCCC[A/G]ATTAGCTAGGATTAC | 221178 |
rs114834484 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250948 | TACTATAACCTAATG[C/T]AGGGAATTGAGTGGG | 221178 |
rs114835487 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173603 | GTTTTCTATAGATGT[C/T]CATTATCAAGTTGAG | 221178 |
rs114843150 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275496 | AAGGGTGTGCTCCTT[C/G]TACCTGACTGAAGCT | 221178 |
rs114867925 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067201 | TTCAGTCTCAGTCTT[C/T]ACACTTTCCCCATCC | 221178 |
rs114889974 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261192 | GAGACCTCGGGAGTC[C/T]GTTGCCTCGGAAAAT | 221178 |
rs114924088 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050298 | TGGTAACAAAAGACT[A/G]AAATCTTTAATGCAC | 221178 |
rs114937705 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155298 | ACAGAGATCTGTCAC[G/T]GAAGAACTTTAGGGC | 221178 |
rs114953269 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253049 | GGAGTTAACTTATTA[C/G]GAGTTAGTGACTGTC | 221178 |
rs114954429 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295945 | CAAGCAGGCACCCTG[A/G]CTTCAAAGTCCGTGC | 221178 |
rs114955292 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111692 | ATTATAGACATGAGC[C/T]GCCATGCCCGGCCTG | 221178 |
rs115001047 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051503 | TGGGACATACTCATG[C/T]ACACCCAACCCTTAG | 221178 |
rs115013593 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060757 | AGAGAAAAGCAAACA[A/G]CTCCATTAAAAATGG | 221178 |
rs115014327 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079506 | CCTGCTACCTGGTTG[C/T]AGATTGCTTTCAGAG | 221178 |
rs115021316 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257518 | AGAGAAAATGCCCTT[C/T]TTGAGGGGACACAAA | 221178 |
rs115033013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203706 | TCTTTTTTGTTGGTA[A/G]GTATTTGGGAGAAAG | 221178 |
rs115037833 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212868 | CTGAAGTTGCTGCCG[C/T]TGGGAGAAACCACAG | 221178 |
rs115039303 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051270 | AGGAAGTGATTTCCA[A/G]TCACGTTGGACATGC | 221178 |
rs115044134 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273548 | TTACATTCTGGAACA[C/T]GAAACATATTTCATA | 221178 |
rs115058566 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129273 | AAGTCTGAGTACAGC[A/G]TCTGTCCCATGTGAG | 221178 |
rs115062347 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086052 | AAGGTGAGTAGCAGA[A/G]AAGTTTCACTGTGGG | 221178 |
rs115064452 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171304 | AGACGAAGGAAGATG[A/G]TGAAGTCGTGACCCT | 221178 |
rs115097808 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995604 | GGTCATGGAATTTCA[C/T]CTGTATCTGATATGC | 221178 |
rs115104008 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167584 | AATACTTCTGTGTGA[A/G]TAGTGTGAATGGGAA | 221178 |
rs115113968 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160210 | CTTCCCGCCCTGGGG[A/G]GTGGGGGCTGGCTGG | 221178 |
rs115123089 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986151 | AGCATACCATGGTCT[C/T]GCATGTACACATTAG | 221178 |
rs115124120 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006615 | GTTGACTGGACCCTA[A/G]CTCTGGGAGGTGCCG | 221178 |
rs115124631 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022767 | GCCATGTTGTTTTCA[C/T]TGATGACTACTTCTG | 221178 |
rs115133986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028173 | TACCCTATTATTATT[A/G]TCTTCTACTTAGGCT | 221178 |
rs115145306 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083521 | AGAATGGCTAGCTCT[C/T]TGTGGAGTTGAAGGT | 221178 |
rs115167895 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276546 | TGTGTGGCCGTTCTG[C/T]AAGATGAAAAAGTTC | 221178 |
rs115183581 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048948 | GGAAACTCAAAGAAA[A/C]AAATGACAAAACAAA | 221178 |
rs115194894 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186971 | TGGGTCAGATGTGTA[A/G]GTGTTGATTTATGCA | 221178 |
rs115195221 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009000 | GAGGTGCTGAGCAGT[G/T]GCCTCAGCCAGCGGG | 221178 |
rs115197662 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205445 | AGAAATCAGAGATGC[A/G]AATGGAAAAACACTC | 221178 |
rs115200801 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188830 | GACACAATGATTCTC[C/T]GGTTAGGGGCTAATG | 221178 |
rs115228509 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121335 | ACAAAATTGCTAGTT[C/T]GTTTTTCAATTAATA | 221178 |
rs115230096 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257814 | GGAAACAACCAAAAA[C/T]TGAGTCCTTTAAAGG | 221178 |
rs115235638 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145933 | GAGAAAGAAGGGGGA[C/T]GAGCACTCCCGACCA | 221178 |
rs115243840 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039573 | CATTTTTCTTTCTCA[A/C]TCTCAATAGGAATTC | 221178 |
rs115245921 | snp | C/T | 0.314544 | 0.241524 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211733 | ATCCGGTGGCACTGA[C/T]GATGATGGCCTCTGC | 221178 |
rs115248312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302061 | TTCCATTTAGAGCAT[G/T]TTATTGCTACTCACC | 221178 |
rs115253338 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016900 | CCCCGCCCAGGCTCA[C/T]GCCCAGCCTTCAATG | 221178 |
rs115263808 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043412 | TCATTTGTAGCAACC[A/G]TGGGGATACTCAGGA | 221178 |
rs115333986 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081906 | TACCTGGGCCCTGTT[C/G]CCTGGTGCTGGTGCT | 221178 |
rs115344643 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066704 | CCCCACCTTCATTCC[A/C]CTCCTCACTCTTTCA | 221178 |
rs115346572 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204773 | TGCTGTAGCATGAGT[C/T]AGAATTTCTTTTCTT | 221178 |
rs115354534 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149558 | GGAGTTCTGCTGCCA[C/G]TTTTTCAGGAATCAG | 221178 |
rs115361849 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199165 | AAGTTCTGGGATTAC[A/G]GGCCTGAGCCACTGC | 221178 |
rs115366341 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194069 | CCATGGTTCAGTAGC[C/T]GAGTCTGTGGTGGGC | 221178 |
rs115379576 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065365 | GGCAGAGCATGTGTG[A/G]GAGGGCTGTGAGCCT | 221178 |
rs115379667 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236104 | CTGGGTTTCCAAATG[A/G]GGAAGGAGGCCTAGA | 221178 |
rs115382134 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013973 | GACTCGATGTGCAAG[A/T]CTGGAGTGTGCTAGA | 221178 |
rs115385620 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251278 | GAGTAAATGAGGCTG[A/G]AGAAGGATGTGAGGA | 221178 |
rs115395221 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162207 | CTCCACCCAGTTCTC[C/T]CATCTCCTTCCTTAT | 221178 |
rs115399535 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187851 | AAAGTAGGCCAATTA[A/G]TAACTCTACAATAAC | 221178 |
rs115399829 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134508 | GGCAGCTTAAGCCAG[G/T]CCTGGATTAGCAAAG | 221178 |
rs115405543 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019858 | TTAGCGTTCACAGGC[A/G]TAGATTTCAACATGC | 221178 |
rs115422182 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000975 | CTGCTGTAACATAGC[A/G]CCACTGTTTTTCAGC | 221178 |
rs115468928 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049698 | CGAAACTGATGGGCT[A/G]TGAAGGGAGTGGATG | 221178 |
rs115478316 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148941 | ACCAGGAAATGCTCT[C/T]CTATGCATGCCACAT | 221178 |
rs115484716 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141531 | ATCCTTCTCTCTCCT[A/G]TGATCCCAAAACCTT | 221178 |
rs115488964 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250987 | AAGAAAACCTAAGGA[A/G]TTACATAAGCAGGAT | 221178 |
rs115492621 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260162 | GGGGAGCATGTCAGT[C/T]GGATCTGGGCTGTCC | 221178 |
rs115507279 | snp | A/C/T | 0.0166612 | 0.0899761 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067641 | CTCTATGCTGTGTCA[A/C/T]CTCAGGAACAGAATC | 221178 |
rs115519460 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024612 | GCTGCTGATCCCGCT[A/G]TGATGCATCCAGTGC | 221178 |
rs115565111 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214056 | ATCACCTTCTCCAGA[A/T]CCGCATTCAGGTGAT | 221178 |
rs115573940 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241236 | TAGAAAGAGTAACCC[A/C]GTAAATGATGTTTCT | 221178 |
rs115574647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146758 | AAAGCATTTTCCATC[A/G]TGGTCGGCTATGCTT | 221178 |
rs115600958 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062821 | ATTGAGAGAAGTATC[A/G]GGATTTCCAAACTTC | 221178 |
rs115606484 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003552 | CTTAAGAAAACCTAG[A/G]ATTTTAAAAGAAACA | 221178 |
rs115607227 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999019 | CAACCTCTGCCTCCC[A/G]TGTTCAAGCAATTCT | 221178 |
rs115622005 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248242 | ATGGCCCAGCTTTTT[C/T]AGAGCAGCAAAGAAC | 221178 |
rs115622601 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034201 | TGGTCTTGGGCAAGA[A/T]GGGAACTCAAGTAGG | 221178 |
rs115641322 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082907 | AAAAACTTCTAAATC[A/G]TCTCAGTATGGAAGG | 221178 |
rs115643862 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276045 | CTGTTGGTGGGAATG[C/T]GAAATGATGCAGCCA | 221178 |
rs115656576 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242601 | AAATGGGGGTAATTA[C/T]GTCTTCTTTGCTTCT | 221178 |
rs115663047 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292723 | AAACTTCTGGCCGGG[C/T]GCCATGGCTCACGTC | 221178 |
rs115689976 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211093 | ATAAATTCAACTGAT[G/T]TTTCCATGTTGATAT | 221178 |
rs115698170 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220996 | TTGTTCCTCTCTTGC[C/T]TTTGGCCTCTGTGGC | 221178 |
rs115706984 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043007 | CCTTTCGCAATGTGT[A/G]TCTTAGTGAATAATG | 221178 |
rs115711176 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001694 | AGTTTTGGATACTGG[C/G]AGGGATGTTCAATGA | 221178 |
rs115730901 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048568 | TTTCTCTTATTTTTT[C/T]CTCCTTTGTACTTTA | 221178 |
rs115765591 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150042 | TCCCACAGAAAGCTG[A/G]TATCTGCCTGACTGG | 221178 |
rs115772605 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253268 | AGAAAAATAAAACAG[A/G]ATAGAGAGCATTCAT | 221178 |
rs115786558 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004508 | GGGGTGAGGGGCTCC[C/T]CACAGGGGCGCAGAC | 221178 |
rs115796734 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143247 | AGCAGGAAGTCTAGA[C/T]GGAAGCCCCTGGTGT | 221178 |
rs115799956 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099992 | TGGCCCAGGGTCCAC[A/G]GAGGGGCTTCTGGTG | 221178 |
rs115818493 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013663 | CGCTTTCATTCCTTA[C/T]CACCCACTTGCTCCT | 221178 |
rs115821224 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048830 | CTAGAAGACCTTGTA[A/G]CAAATTTATCGCATC | 221178 |
rs115823725 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061458 | AATAGCAGAGACATG[A/G]AATCAATCTAAATGC | 221178 |
rs115832425 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089921 | TCTGGAGGGGCCAAA[C/T]GCTGTGTTTTCACAT | 221178 |
rs115870614 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284789 | TCCCCATCAGTGTTC[A/G]GCCAGTGCTTTCCAC | 221178 |
rs115880414 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208898 | TCTTATACTGAAGAT[C/T]GGATATTGGTGTTTT | 221178 |
rs115906885 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051299 | GCTGTGCCTGCAGCC[A/G]GCAGGACTTCCTGGT | 221178 |
rs115921848 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289692 | ATGCGGCTCCAGGAC[A/G/T]CATGGTTGTGATACT | 221178 |
rs115933818 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053865 | TGGATTCTTGTTAAT[A/G]CCATGAAGTAGGAAT | 221178 |
rs115942882 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112795 | CCTTCCATGTCTCGT[A/T]GTAGTATGATTTGGT | 221178 |
rs115943848 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151540 | GTTATATACATGAAA[A/G]TCCTGTCTCTGTCAG | 221178 |
rs115953846 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246578 | GAAAAATGTGACTCA[G/T]GCCGGGTGTGGTGGC | 221178 |
rs115991479 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195264 | TCAGTGTGCATTCAT[A/G]TTGTAGCATAGCATG | 221178 |
rs116006132 | snp | C/G | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191308 | TATGTACATTTTTTT[C/G]AAACATAATGCTATT | 221178 |
rs116021763 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194083 | CCGAGTCTGTGGTGG[A/G]CACCTCATTGATCTT | 221178 |
rs116028023 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227625 | ACCCAGGCTGGAATG[C/T]AGTGGTGCGATCTTG | 221178 |
rs116035566 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250865 | GAACAATAGTCCAGG[A/G]TGCTCCACAGCCTTA | 221178 |
rs116047237 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085335 | TTTCGCCATGTTAGC[C/T]TGGCTAGTCTCTGAT | 221178 |
rs116052656 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100922 | CGTTCTCTTGATATA[A/C]ATCTTCACTGGGTTT | 221178 |
rs116059048 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125637 | CAAGGAATTCTTCCT[C/T]GACTTAGGTGAGATT | 221178 |
rs116069012 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246992 | GCTTTCAGGAAAATA[C/T]GTGAGTTTTGTGACA | 221178 |
rs116087041 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157006 | TTACTGACAAAATCA[C/T]CTGGAGAATGAGTGC | 221178 |
rs116092173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188751 | TTCTAGAGGAAGAAG[A/G]TGCCATTCTAGGATT | 221178 |
rs116094216 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139140 | CTAGGAATCCTTGCT[A/G]TTCCTGGGTCTACAC | 221178 |
rs116107732 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253342 | CACCTGTTCCATGAA[C/T]CCTCTCTCTCTTCCC | 221178 |
rs116117078 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990322 | GCCACCACTCCCCCA[C/G]AATAAAGCTCAAACT | 221178 |
rs116146223 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129834 | TTGTGCCTGTTGTCC[A/G]TGTCCCCTGGGCTGA | 221178 |
rs116156282 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006588 | TACTAATTCATCACA[A/G]TTGCAGGTGTGGTTG | 221178 |
rs116160230 | snp | A/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977898 | TCTTTTTCTTTTCTT[A/T]TTTATTTATTTATTT | 221178 |
rs116165205 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169011 | TATCAGATTCAATAC[A/G]TTTTACTTTTCTAAA | 221178 |
rs116168582 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192915 | AGCACTGGTAGAGAT[A/G]GACAGGAGGAAAAGG | 221178 |
rs116174621 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043301 | TAGGAGTCCAGGTAC[C/T]TATGTGGTGGATGCT | 221178 |
rs116175311 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063710 | AGGGGGCAGCCTTCT[C/T]GTTGCTGATGTTTCA | 221178 |
rs116179044 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092364 | TATTTCTCATACCCC[A/G]TAGTAGGCCTTTATT | 221178 |
rs116197101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098082 | CTATTAAAGACCAGG[A/C]CCCAGAGAAAAACAA | 221178 |
rs116200228 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122617 | CTTCTCCTGCAACTC[C/T]TGTAAGAACCTTTTT | 221178 |
rs116214609 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051478 | TTGCACCTGCCTGGG[C/T]GATGGCACTTGGGAC | 221178 |
rs116253231 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258310 | AGTGTCACAGATGTG[C/T]GAAATTGGTCCTTGT | 221178 |
rs116272445 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018604 | TAGCCAATGATGACA[C/T]AGAGGCACAGCTAAT | 221178 |
rs116278243 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214024 | TTTGGTTTCAGAGGC[A/T]TCCTTTGGGAAAAGC | 221178 |
rs116284400 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049463 | GTGTGAGTACGCTCC[A/G]TGTTGTTCACACAGC | 221178 |
rs116295907 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258908 | CACTACTCAGGTCCA[C/T]GTCAGGAGCTTTGTC | 221178 |
rs116328253 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040443 | GTATGGAGTGTAGAA[A/G]TTCACAGCACCGCCC | 221178 |
rs116329185 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167521 | CCTCACCTCTCAACA[G/T]TACAAGCTTGAATTC | 221178 |
rs116332496 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194377 | TGCAAGAGTAGGACA[A/G]GAAGTGGAGAGGAAA | 221178 |
rs116364590 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146603 | ATAACCTCTAAAATG[G/T]TCTTTTACAGGGCAC | 221178 |
rs116372891 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253878 | GGAGCAAGAGGCAGA[C/T]GAGGATGTTGCAGGC | 221178 |
rs116373342 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220404 | AAGAAGACCATTACT[A/G]CTAATGTCAGTGCCT | 221178 |
rs116377365 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001220 | GTAGTCACATATACA[A/G]GAACACGGGGGAAAG | 221178 |
rs116402752 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104010 | CAATGCTTACTTACT[C/T]TTTTCCTGCAGCCTT | 221178 |
rs116424804 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169742 | GAGGTGAGGGAAGAA[A/G]GTAACCTCCTGCAGA | 221178 |
rs116426583 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213831 | GTCTTCAAGTCTGAA[C/T]AAGTGACTTAAAAAT | 221178 |
rs116444992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258539 | CCAAGAGTTGTCGTG[C/T]GTTCCTGTAGTACCA | 221178 |
rs116446186 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289396 | ATTTTTTCAAAATCC[C/T]TTTATGTAGTCTGGA | 221178 |
rs116476058 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187455 | ACAGCGACCGGCTTA[C/T]GTTTTATTCTGCCTA | 221178 |
rs116502291 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287550 | TCATAGAAGGCAACA[C/T]CCTCACTTGATTTTA | 221178 |
rs116511406 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100846 | AAGCTTCCCACCCTC[C/T]TTCTGGTGAACTCTT | 221178 |
rs116543355 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052039 | CCTACCAGCTGGTGA[A/G]GAGTCCCTGTGTTTG | 221178 |
rs116544235 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084487 | ACTTCAGCCCTCTTA[A/G]CACCACCTGGGTTTC | 221178 |
rs116557466 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979797 | AGGGCGCAGGGCATG[A/G]GGGCGGCGCGCACCC | 221178 |
rs116563350 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164906 | AGTTCCCAGTCCAGC[C/T]GTCGCGCTAACTTCG | 221178 |
rs116570351 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192332 | CAGGGGCTTTTTCCT[C/G]TAGTTCTCTGCTTGT | 221178 |
rs116570947 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210329 | GCTTTTAGTGTTATA[A/T]CCAAGAACTTATTGC | 221178 |
rs116599728 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031429 | GAGTCCTTTTCGGTA[A/G]CTTGTGTCCACTTTC | 221178 |
rs116600224 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050996 | TTTCCAGCTGTTTTT[A/G]CAGGTGAGTGTACTG | 221178 |
rs116606167 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285513 | CCTGCCTGCCTGCCT[G/T]CCTCCCTCCCTCCCT | 221178 |
rs116630362 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007203 | TGGCCCTGAGGCTCT[A/G]AGCCCTCTGCAGAGT | 221178 |
rs116645769 | snp | C/G/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278388 | CTCCACAGCTTAAAT[C/G/T]AGTGCCTAGCACATT | 221178 |
rs116656783 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095608 | AAAATAAATATTTTT[A/G]AAAAGAAAAACCACC | 221178 |
rs116675050 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124309 | TTTCTCATCTATAAG[A/T]TGAGGAAGGTAACAG | 221178 |
rs116698229 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208030 | TAGGGAAGTTGGAGC[C/T]GCACTGCCTGATGGG | 221178 |
rs116719333 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986188 | CGGCTCGCCCAGGGA[C/T]CTAGTCATTGTATAA | 221178 |
rs116768000 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129009 | TGACAAACTCTACAC[C/T]GGGGTAAGTGACCCT | 221178 |
rs116789308 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204871 | AACATTTGGGTTGTT[C/T]CTGCCTGTTGGCTGT | 221178 |
rs116799267 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042808 | ATCTTACCAAGCTCT[C/G]CCAGTTCATTCTAAC | 221178 |
rs116804943 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162611 | TTCTAGAATTAATGT[C/T]AATATTGATGTTAGG | 221178 |
rs116813461 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014645 | TCTGTTAGTTTGTAA[C/G]AAAATAGTGTATGTC | 221178 |
rs116819316 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119848 | CAGAGCTAATTCTCC[A/G]TCAGTCTATGCATGC | 221178 |
rs116837499 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068443 | GTGCTGAACATACAC[A/G]TGCTTGTGTCTTTAT | 221178 |
rs116856999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272279 | CTCCAGCTCTGAGCG[A/G]TGCTCCCTCGGTGCT | 221178 |
rs116863170 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209924 | CACATCCTTACCACC[A/G]CTTGTAACCTCTGGT | 221178 |
rs116933171 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141771 | GTGGCTAAGAAAGAT[C/T]GAGAGCTATCATTAA | 221178 |
rs116938466 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085031 | CGCCTGTGTGTTCGC[A/C]GTCGCCTGGGATTCT | 221178 |
rs116952012 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290042 | AGGCCTCCTTGTGTG[A/G]CCTGTGCAGAAGGTT | 221178 |
rs116952894 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031684 | AATAGCTAAGACCTC[A/T]TATGACCTGCCCTTG | 221178 |
rs116998642 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989289 | TAGCCAGGAGTAGTA[A/G]CATGCGCCTGTAGTC | 221178 |
rs117006076 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134055 | GGGAGGTGGGGAGCA[A/G]GTAGGAAGATGTAGC | 221178 |
rs117017717 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130588 | TCAGACAAGATCAGA[A/G]GTTTAAAGGTGGCCA | 221178 |
rs117044780 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175870 | AGAGCGATTACTAGA[A/C]AACATAAATAAATTT | 221178 |
rs117048764 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269120 | ATTTATTAACCCCCA[A/G]TGAAGAGCCAGTGCT | 221178 |
rs117065930 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290211 | TGGGAAGAGAGGTAT[A/G]TTGAAATGGGCATTT | 221178 |
rs117068845 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116215 | AGCGTCTGCTAAGCT[C/T]CTGCTTTTCATGGAT | 221178 |
rs117081022 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061828 | CCTGAGTTTATTTAT[A/G]TAACAGACTTCAAAT | 221178 |
rs117109007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062606 | CAGTTCTAATTTTCC[A/G]TTTTCTTATAGAAGT | 221178 |
rs117110160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062489 | TCCCACCAGCCCTGC[C/T]GCTCCAGGGCTCTGT | 221178 |
rs117112588 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003438 | GGGTACTGTGCATGT[C/T]TTCATGAGGAACCTG | 221178 |
rs117112767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188990 | TTTAGCCCACTGTTG[A/C]GACCTACTGTTTAGA | 221178 |
rs117131065 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230118 | TGTGATTGGAGAGAA[C/G]AGGAAGTAATGTAAT | 221178 |
rs117142783 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195822 | GCTAAATATTAACAC[C/G]TGTTAACAAGTTGAC | 221178 |
rs117145484 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997147 | TCTGCTTAAACAACC[A/G]TCAGTTTCAACTGAA | 221178 |
rs117146018 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140614 | GCCCCTGCTCTTGTG[C/T]GTGTCCTTCTGAGAC | 221178 |
rs117149646 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008902 | AGGAGGAGGGAAGAG[G/T]GGGGAAAGCATAGCT | 221178 |
rs117162902 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050602 | TGGCAGCTGGCCAGG[C/T]CTCAGCCCTGGACAA | 221178 |
rs117180566 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070637 | GTGTGTTTCTGTCAG[A/G]ATGATTTTGGATGAG | 221178 |
rs117183556 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287768 | GATTTCAGAGAACTT[A/G]TCATTAGTAGAGGTG | 221178 |
rs117190613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296396 | GTCATACCAAATACC[A/G]TAAAGTAACATTGGA | 221178 |
rs117197525 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192802 | CAAGGATTTTGAGAG[G/T]GTGACATGGGAAAAA | 221178 |
rs117208170 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131438 | ACCTGGGCACTGAAG[C/T]GCCTTATCTTGTTTA | 221178 |
rs117219201 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097066 | AACAGCGTTGGCCCC[A/G]GCTGAAACGGTGCCA | 221178 |
rs117227243 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135904 | ATATTAGCCTCACAA[A/G]AGTTTGCAAATTCAG | 221178 |
rs117228139 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037365 | AATTTTAAAAAAATT[A/T]AAAAAAAAAGAAAAG | 221178 |
rs117231099 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215906 | CAGTCTTGTGGTGAC[A/G]TCAGTTTTGGCATGG | 221178 |
rs117236315 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114615 | TTATTTTCGAAGGAG[C/T]TCAAGGTCAAACTCT | 221178 |
rs117242381 | snp | A/G | 0.000271506 | 0.0116481 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223732 | AGAGCTCCTTTAAGC[A/G]GAAGTCCACCTCCAA | 221178 |
rs117248550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076562 | TGAATATGAACGAAG[C/T]AGCAGACCCCGGGAC | 221178 |
rs117269110 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121758 | GCTGCCTTCATGACA[A/T]CCCCTCGTGTTTCAG | 221178 |
rs117280090 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278342 | TACCTCCCATGTAGC[A/G]TTGTCATGAGGATTA | 221178 |
rs117284695 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082001 | TCACTGAGTGCTGCT[A/G]TATTGGTCTCGAATG | 221178 |
rs117289266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263811 | AAACGAGATGAATCA[A/G]TTCACTTATCAGTAC | 221178 |
rs117318200 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129543 | ACCCTGAAATTAGTA[G/T]GGACAGGTTTGTTAT | 221178 |
rs117325722 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070762 | AGGCTGACCCTCCCC[C/T]AAGTAATGAAGAATT | 221178 |
rs117337861 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212789 | GGATAGGCAGGCTCA[G/T]CCTCCTGAATCTTGC | 221178 |
rs117349345 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149204 | CAGTGTGTTCCAGTG[A/G]TGGGCTTTATCTCAT | 221178 |
rs117356165 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114320 | GAATTGATTGAAAAC[A/C]AATATGCGAGCATAT | 221178 |
rs117360034 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094688 | TGCCTGAGCCCAGGA[A/G]TTTGAGGTTACAGTA | 221178 |
rs117370629 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029112 | AGTTTTTGTTAGTAA[C/T]GGGGTCTCACTGTGT | 221178 |
rs117376545 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041174 | ATTCAACCCACAGTA[A/G]CTCAGAACCACACTG | 221178 |
rs117409049 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070912 | CTCAGCTCTCCCAGG[C/T]TTCCAGGCTGCCAAC | 221178 |
rs117413394 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298883 | ACTTGGAAACACTCA[A/C]TGGGTAGACATTGGC | 221178 |
rs117420216 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175212 | TTGCTACAGACTCAG[C/T]AGTGATGCTTGTTTT | 221178 |
rs117484249 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114953 | AGGCATGAGCCACTA[A/C]ACCCAGCCCCTTGGC | 221178 |
rs117487931 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049283 | TTATAATACCACATT[C/T]CTATGCCTTTTCTAC | 221178 |
rs117501111 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178990 | AGTCTGTCCCTCTAC[A/G]TTTGACTATTCTAGA | 221178 |
rs117519788 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198283 | CAGGCGTGAGCCACC[A/G]CACCGAGCCACCTTG | 221178 |
rs117520404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281125 | ATGCCCCTGGCAACC[A/G]TCCCCTCTCCTTTAA | 221178 |
rs117523785 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121476 | CATTTCCTGATTTTT[A/G]TAATCAGTTATGTAG | 221178 |
rs117526964 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106273 | TCCTGGCCTCAGTGA[C/T]CTTTCTGCCTTGGCC | 221178 |
rs117539845 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064546 | CCAGAGAACTCCCAC[A/G]CCCTTATTGCCATGT | 221178 |
rs117568225 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129391 | AAAATTGCCAAAACA[C/T]ACAGAACAAGGCTTG | 221178 |
rs117574889 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303006 | TACACAGAAACACCC[A/G]TGACCCACTATGAGA | 221178 |
rs117609617 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123717 | TCCTCATCAGCATCT[A/G]TATAGCACATCAGTG | 221178 |
rs117623643 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214962 | CTGACATATTTAAAA[C/T]ATTATTAAGCTGTGT | 221178 |
rs117630957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248289 | GTCTCACCATTGTTG[C/T]GTCTCATCCTTCTAA | 221178 |
rs117643380 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143526 | GCAAAGATGAGTGAC[C/T]GAAAGCAGAAAAGAA | 221178 |
rs117648242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981711 | ACTCAGAGAAGTGCG[A/G]TGATAAGCCTCATGT | 221178 |
rs117655769 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179705 | GATTCTAGCCAGCTT[A/G]ACTAATGTGTCTGAA | 221178 |
rs117675636 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154144 | AAAAAAAGCTTGGCC[A/G]TAGCTACAGAAGGTA | 221178 |
rs117690979 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265184 | CCCTCCTGTGGTGAA[C/G]AGTCTGTGGCTGCTG | 221178 |
rs117702425 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163495 | TTTAGCTGGACAGAT[C/T]TTTATGGTCTCTGTT | 221178 |
rs117708681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269018 | CAGCTTTCCATTCTG[A/G]GTTCATGCTGTGATT | 221178 |
rs117734224 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070763 | GGCTGACCCTCCCCC[A/G]AGTAATGAAGAATTC | 221178 |
rs117740195 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078679 | AGGAAGCAGTTGTCG[A/C]CCTAGTCCATAAAGT | 221178 |
rs117742994 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993627 | TTCCCACAGACCCCT[G/T]CGTGACATTGTTGGA | 221178 |
rs117756516 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099703 | GCACAGAGGATGAGC[A/G]CCATGTGATCAGTGT | 221178 |
rs117779147 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245825 | AATTCCTGGGCTCAA[A/G]CAATCCTCCTGCCTG | 221178 |
rs117784668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299998 | GGGTGGAACTGCTAA[C/T]GTGCAAAGCTCTCAT | 221178 |
rs117802275 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163968 | AAGAAATGTTTGCCT[A/G]TGAGACATGTAATAG | 221178 |
rs117831614 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200500 | GAATGTCCCACCTCG[C/T]TCTCAGCCCCAAGTC | 221178 |
rs117832149 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152390 | GGACTCAGTGGTTCC[G/T]GCTCAAGGACATGGC | 221178 |
rs117836997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276421 | AAGGACATATACTGT[A/G]TGATCCCATTCATAT | 221178 |
rs117838884 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034587 | CCGTTTTATTATTCC[C/T]CAGAGTTCTATGCGT | 221178 |
rs117855043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157642 | GGGGCGGAAGCCATA[C/T]GGGTTACTTTATAGG | 221178 |
rs117859598 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197955 | ACTGTTGTTCTTCCA[A/G]CTCCTCACTTTCCCA | 221178 |
rs117876184 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987302 | GAATATGTCTATGAC[C/T]GGGAAATGAGGAGCC | 221178 |
rs117880856 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116111 | AGGCTGCTATGACAG[A/G]ACACCATGAACTGAG | 221178 |
rs117884848 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001227 | CATATACAAGAACAC[A/G]GGGGAAAGTAACAGT | 221178 |
rs117900647 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068070 | ATAGGTAAACTTGTA[A/T]CATGGGGGTTTGTTG | 221178 |
rs117901514 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199609 | TTCCTTAGAACTGAA[C/T]GTACTACTTTTAATT | 221178 |
rs117913285 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081660 | GCCTGGGTGACAGCA[C/T]AAGACTCTCTGTCTC | 221178 |
rs117920968 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23983813 | TATCTGCATTTTTTG[A/T]GCTGCAGAGTGATGG | 221178 |
rs117921802 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213504 | ACTCCCGACCTCATG[A/G]TCCATCTGCCTCGGC | 221178 |
rs117925487 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004170 | AAAAATCTCCAAAGC[A/G]TCATGAACCCCGAGT | 221178 |
rs117928251 | snp | C/T | 0.0256215 | 0.110247 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979594 | CAGCAAACAATAGCA[C/T]AGCCCCGGCCCTGGA | 221178 |
rs117928578 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122662 | TCACTTCAAGATACT[C/T]GGTGACAGACAGAAG | 221178 |
rs117945245 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051195 | TTCTGCTCCCCAGTC[C/T]CCACGCAGCACATAC | 221178 |
rs117949293 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239518 | TGGGCAACATGGCGA[A/G]ACTCTGTCTCTGCTA | 221178 |
rs117952939 | snp | C/G | 0.0659589 | 0.169201 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247587 | CGTGTTCAAGTGACT[C/G]TCCTGCCGCCTCAGC | 221178 |
rs117968582 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007045 | TCTGAAGGCCAGCTT[A/G]TGCACAAGGCCTCCC | 221178 |
rs117972266 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124256 | TTTTTGTTGTCTTTA[A/G]TAGTCTATTGACACC | 221178 |
rs117982760 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281144 | CCTCTCCTTTAATGA[A/G]CAGGTAAGAAAGCTA | 221178 |
rs117987915 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045517 | TCACATAATACACGT[A/T]TTTTAAATTGTTACA | 221178 |
rs117997129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208309 | GGCTGATAATAACCT[A/G]TGTTCCATATTCCTG | 221178 |
rs117998823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002614 | GGACTGACTAGACTG[C/T]AGGAGCTTCACGAAT | 221178 |
rs118027138 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243278 | TCTTACTTTACAGTC[C/T]TCTCTCATTTTCTTT | 221178 |
rs118027646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169603 | CCCTTCCCGAGGTCA[C/T]GTGGCTCCGGGAGCA | 221178 |
rs118036487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112688 | TAACAGGAGGTGCTG[A/T]TGTCTCAGTCTTCAT | 221178 |
rs118040972 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108110 | GTGCCCTCTGGAGGG[G/T]TGAATGCTGTGCCAT | 221178 |
rs118077638 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185865 | CATGTGATTGTGAAG[C/T]CTGGCAAGTTCAAAA | 221178 |
rs118087919 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004612 | GCTGGCTGTGGGCAA[C/G]AGACCCTGCCCCAGG | 221178 |
rs118088430 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24035015 | TTGCCAAGAAATAAA[A/G]CTCTACATGACACAT | 221178 |
rs118092037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009273 | GGTCCTGTGAACCAA[A/G]AGTATCTGAGATACG | 221178 |
rs118098183 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118146 | ACAGCACGTAACTCC[A/G]AACCTGAGCGTAGAC | 221178 |
rs118099477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013996 | GTGCTAGAGTCAGAG[C/G]CTCCAAACCCGTCAC | 221178 |
rs118101184 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277172 | ACCTTGGGCCGGGCG[C/T]GGTGGCTTACGCCTG | 221178 |
rs118113088 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129575 | TGGCTGAATCACCTG[C/G]CTGGTGCCTGCCTGA | 221178 |
rs118120495 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292283 | CCATGGGAAAATGTC[A/G]TCACAGCACAGCCCA | 221178 |
rs118132163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185341 | TTAGTGAAGTACTGC[C/T]ATGAGGATGATTTTT | 221178 |
rs118155861 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071534 | CCTGTATCCTCAATC[A/G]CTTCTGTCTGGTGGA | 221178 |
rs118162355 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294237 | CGAATGCCATACTGG[C/T]ATTTCCGTAACTCAC | 221178 |
rs118170712 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174491 | CCTCACAGCACTGCT[C/T]TCGCTATATTCCACA | 221178 |
rs118173508 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083232 | CCCTAGGGCAATAGA[A/G]TAGAAAGGCACCTTT | 221178 |
rs137856331 | in-del | -/TG | 0.0452528 | 0.143452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185392 | TTCCTGATTCAAGAC[-/TG]TAATTTATTCTTAAG | 221178 |
rs137863876 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058665 | GATAATTTATTAGTT[A/G]CTTATTTTTAAGTTT | 221178 |
rs137875212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249170 | CCACCGCATCCGGCC[A/T]GTGCTGATTTTCTTA | 221178 |
rs137876116 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208649 | GTTCCCAGACATTCT[C/T]AGTTCATGCACCCTG | 221178 |
rs137898967 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148273 | GGCTCTGGTGATGAA[A/G]TCCTCAGGGTTCAAG | 221178 |
rs137908821 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214268 | CTAAGGCCAGATGCA[G/T]GTACAATAAACTTAA | 221178 |
rs137923002 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135719 | AAAAAAAAAAAAAAA[-/G]AGTATTTTTAGATAG | 221178 |
rs137928642 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061039 | GCAAGACTCTGCCCC[G/T]CACCCCCCAAAAAGT | 221178 |
rs137932470 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152482 | ACGACCTCCTCTTCC[A/G]CCTCTTTGATAAGCT | 221178 |
rs137944039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122096 | GCTGGGCCTCCAAAA[C/T]TGAAAGAACTTGGCA | 221178 |
rs137960297 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277833 | AAGCGTGGGGAATCA[C/T]AGAAAACCACCAGGC | 221178 |
rs137963989 | snp | A/C | 0.00795532 | 0.062565 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24305086 | GGAAGTAAAGAGAAT[A/C]ATTTGCTTGTGTTAC | 221178 |
rs137973523 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115694 | ACAGTGTCAGAGGGT[C/T]GGGAACACGGGTGCC | 221178 |
rs137979505 | in-del | -/CT | 0.0678174 | 0.1712 | intron-variant | SPATA13 | GRCh38.p7 | 13:24270992 | GTTGCAGTTCTTCCC[-/CT]CTCTCTCTCTCTCTC | 221178 |
rs137982173 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087900 | CCTGGTCCCACCGGT[A/G]GTCTTGCCCATTGCT | 221178 |
rs137983843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053797 | ACCAAAACAACCCCT[C/T]AGTTTTCTTGATGGC | 221178 |
rs137987283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176921 | GACGTGTGCCACCAC[A/G]CGCAGCTTATTTTTG | 221178 |
rs137997619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990170 | TCCCTGCTGGATTCC[C/T]TCAGCCACCTCCAGC | 221178 |
rs138009618 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077409 | GTGATCATACTGGAA[C/T]GAAAGAACAGATATA | 221178 |
rs138019628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140362 | TTGCCCCAGCAGACA[A/G]AGAGGATATTTTCAA | 221178 |
rs138030723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265498 | ATTTCCTGTGAAGGA[C/T]TCTCCCATCCCAACT | 221178 |
rs138042100 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206905 | CAAAAAAAAAAAAAA[-/AA]GATACATGCATGCAT | 221178 |
rs138090863 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237276 | GCTGAGGCAGGAGAA[C/T]CTCTTGAACCCAGGG | 221178 |
rs138092454 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269631 | TGGAGTACAGTGGTA[C/T]GATCATAGCTTACTG | 221178 |
rs138096588 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204313 | GTTCAGAAAACGATA[A/G]GAAAATTGTGAATCT | 221178 |
rs138101087 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985164 | ATGCCCTTTCTTCCC[A/G]TCTGCTACCGAAGAT | 221178 |
rs138106208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049226 | AGCATGACAACATTT[C/T]AGTCACTGATGCCTC | 221178 |
rs138120507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079791 | TCTTATAGAATTGCA[A/G]TTTTGTACTTTCTGA | 221178 |
rs138123583 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168213 | TAAGACTTGAGTAAG[C/T]GACCCATAGCCGGTG | 221178 |
rs138131830 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257065 | TTTTTGTACTTAACA[C/T]TGGGTTCCAACCATA | 221178 |
rs138140758 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260086 | AGTGTTCCTACAGAG[A/C]TGCCAGTGTGGTGGA | 221178 |
rs138143126 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104754 | ATAGTAAGTGCCATA[G/T]ATTTTGATATAATAA | 221178 |
rs138151619 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273181 | CAAAGAAGCCCAGAG[A/C]CAACGACGCCCCAGC | 221178 |
rs138154682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207190 | CATGGACACATGGTG[C/G]GGAACAACACACGGT | 221178 |
rs138156175 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070705 | TTCCTCCCTAATTTG[A/G]GTGGGTCTCTTCCAA | 221178 |
rs138157388 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23979998 | CAAGCAGCATTTGGC[A/C/G]GAAATCCTGTGCCCG | 221178 |
rs138158099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168325 | GGTTGAATTAATGAC[A/G]TACATGAAAAATATG | 221178 |
rs138175183 | snp | A/C/G | 9.11037e-05 | 0.0067486 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223644 | GTGTGTGAGATTCTC[A/C/G]TGAGGGACCCTGAAA | 221178 |
rs138195676 | in-del | -/GATA | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158720 | TGTATGTGCTAAGTT[-/GATA]GATAGTAAGAGTCTT | 221178 |
rs138197496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235172 | TTCTAAGTTATAGCC[A/G]GAGCAAAGACCTCGC | 221178 |
rs138200014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109348 | CACATTTTCTTAATC[C/T]GGTCTATCATTGATG | 221178 |
rs138211474 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171622 | GCTGTGCTGACTTCC[A/C]CATGTTCAGACAGAC | 221178 |
rs138227617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013464 | TACCTGGGACACTGC[C/T]TGGGGACAGTGCCCA | 221178 |
rs138245069 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132868 | AGTTCCAGCTACTCA[A/G]TATGATGAGGGCACG | 221178 |
rs138247441 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104219 | GTTTGGATTTGTTGA[A/G]CAATGTAAAGCTAGA | 221178 |
rs138255231 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164636 | CCCTAAATGAGATGG[A/G]GGTTCAGGGAAGCTG | 221178 |
rs138261097 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197559 | ACCTTTATAGTTACC[G/T]TTTCTGAAAGATAGA | 221178 |
rs138282162 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065979 | GATTGGTCTGGCCTT[C/T]CTAGGGCTGTTGTAA | 221178 |
rs138283435 | snp | C/T | 6.67958e-05 | 0.00577871 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24286240 | TGGCAACGTGGTCTG[C/T]GCAGAAGCCCTGTGG | 221178 |
rs138293301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219350 | TACTAAGTCACTGGT[C/T]GTTTAAAAAGCATAT | 221178 |
rs138297659 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044293 | GCTGGAGTGCAGCAG[C/T]GCTATCATGGCTCAC | 221178 |
rs138297833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008560 | AGGAGAGCAGGAGAA[A/G]GGGAGGGGAGAGAGA | 221178 |
rs138304571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280937 | GAAACAGTCACCATG[C/T]GTTGTTCAGGCTCCC | 221178 |
rs138310889 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107948 | AGTCCATTTGTGCTG[C/T]TATAGTACGATATCA | 221178 |
rs138312195 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996796 | TTCCTTGGCTTGTGG[-/C]CCCCTCCTCCATCTC | 221178 |
rs138317173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034955 | TCCACCTCTCAATGG[A/G]GAGAGTTCAAAGCAA | 221178 |
rs138325002 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031703 | GACCTGCCCTTGGGG[A/T]ATTTATAATCTTGGA | 221178 |
rs138330078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182604 | GAGGGCACCAGGCCA[A/G]TCCTGAAGGAGCCAT | 221178 |
rs138344450 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284900 | CACATTTTCATCAAC[G/T]CTCTAAGGAAAGATG | 221178 |
rs138369252 | in-del | -/TTTG | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025189 | GAATATTTTCCTATT[-/TTTG]TTTATTTCCTAAAAT | 221178 |
rs138378229 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100041 | TTGCTGACCAGAGTG[C/G]TGGTGACAACAGTAT | 221178 |
rs138385577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013261 | AGCTCCCGCTCTGTA[A/T]GTGGAACTCTGATTT | 221178 |
rs138395874 | snp | A/G | 0.000542133 | 0.0164552 | missense | SPATA13 | GRCh38.p7 | 13:24290883 | ACCACACAGGAACAC[A/G]GGTGAGGGGCATGGG | 221178 |
rs138405816 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290352 | AGGCCCTGCTCCCCA[C/G]CTTCCAGGATGAGCG | 221178 |
rs138431632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057986 | CATGGGATGCAGAAA[A/G]GAGATGTTCATGGCC | 221178 |
rs138447477 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118612 | TGGGTCTGGGGTAGG[G/T]TCTGAGAATCTGCAT | 221178 |
rs138457260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252624 | TTCTCCTCCCACCCC[A/G]TACCTGTGTACACAC | 221178 |
rs138457724 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006967 | GTCATTCTGGGCCAG[A/C]CTCCCCCATCCTGTG | 221178 |
rs138463414 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208065 | GCTGAAAGAGCTTTC[A/G]GCAGGGAAGGGACGA | 221178 |
rs138491462 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246520 | TGTTTATTCACATGC[C/T]TGCGTTTGTGCGTGT | 221178 |
rs138496156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153576 | AACAGAGGACACGTG[A/G]TAGAGAGAATGATCC | 221178 |
rs138497107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192942 | AAGGATTCTTTCCTC[C/T]CCCTGCTGTTCTCAA | 221178 |
rs138501519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089023 | TGATGAGGATGGGAC[A/G]CGTTCACAGGTGGCT | 221178 |
rs138516814 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280417 | CACTGTTCAGTTCTT[C/T]GAGGAGAAAGCGTCA | 221178 |
rs138520873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177323 | CCTGGCCAGAAATTA[C/T]AAATTTATTTCTTAC | 221178 |
rs138537564 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092964 | AGATGACTATTTTCT[C/T]ACACAGAGAATCTGA | 221178 |
rs138540784 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293025 | AAAAAAAAAAAAAGG[-/C]GAGGGTGTGGGGAGA | 221178 |
rs138547000 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024194 | AGGTGACCAGTCACA[C/T]TGTGAACTGGCCCCA | 221178 |
rs138575046 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109418 | GTGCTGCAATAAACA[C/T]ACGTGTCAATGTGTC | 221178 |
rs138577515 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993704 | GAAAGCCCATCCTTT[A/G]GCTAGAGGGAGAGGA | 221178 |
rs138588365 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080433 | CTTGACACCATCACA[G/T]GCATCATCACTCAAA | 221178 |
rs138599456 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144667 | GCAGCACACCAGCCC[C/T]GCTGCAGCAGCCACC | 221178 |
rs138602665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088661 | AATCAAAGCTCAGAA[C/T]CACTGCCTTCCAGAA | 221178 |
rs138610014 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073009 | TCCAACATTGATCCC[A/G]TAGATCTTGTCTCTA | 221178 |
rs138620086 | in-del | -/AAGAAAGG | 0.375598 | 0.21616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276635 | GGGTTAAGATGGTAA[-/AAGAAAGG]AAGAAAGGAAGAAAG | 221178 |
rs138637315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083594 | CTCCTCCATCATTTG[A/C]TCAGAGAATAATATT | 221178 |
rs138645455 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045245 | CAGATAAGATTTATG[G/T]TCTTCTTGTCTTCCA | 221178 |
rs138645993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203576 | TATGTCTAGGTGGAC[A/G]CAGCAATGCAGTGCC | 221178 |
rs138648811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147117 | TGATTGTTCAGATAA[C/T]TTTTTTCTTACCATC | 221178 |
rs138657885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269099 | AGCAGCAGCGTGACG[A/G]CTAACATTTATTAAC | 221178 |
rs138665183 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021292 | GAGAATCCTGAAGAT[G/T]CCTGTTTGCTCAAAG | 221178 |
rs138673272 | in-del | -/CCCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171155 | GAGTGAGACGTTCAA[-/CCCC]CAGCCGCTGACTGCT | 221178 |
rs138674199 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24219049 | AGTTCATACACCCTA[A/G]AATCCAGCTTGTAGA | 221178 |
rs138677091 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092014 | AAATCACCGTTCTTC[C/T]TGACGGTTAGTCATA | 221178 |
rs138687419 | in-del | -/AGAACAGT | 0.00444273 | 0.0469215 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300578 | CAGCTTGGAGCAAGG[-/AGAACAGT]AGAAGTTAGAACTCA | 221178 |
rs138689578 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199185 | TGAGCCACTGCGCCC[A/G]CCAGAACCATAAAAT | 221178 |
rs138692743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985879 | AGCCAGCGGTCCATA[C/T]GCTGAGACGGATGGG | 221178 |
rs138696015 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136582 | GAAATGCTCAGAAAA[A/C]ACTGTCAGATGAATT | 221178 |
rs138702221 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270082 | GTATATATTACCTCA[G/T]TGTTCATAAAGTTAA | 221178 |
rs138716466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993556 | AGTTTCTGCCAAGGA[C/T]GTTCTCGGCCCAGCA | 221178 |
rs138718414 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290471 | CGCCGGCCAGATAAC[A/G]CTTGCGGAAACCATG | 221178 |
rs138725153 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038575 | AGACGTCTTCGGTAA[A/C]GTGCCGAGAGTAAGG | 221178 |
rs138735968 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989373 | GTTGCAATGAGCCGA[G/T]ATCACGCCACTGCAC | 221178 |
rs138748795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273531 | TTTCCAACACTAACA[A/G]TTTACATTCTGGAAC | 221178 |
rs138762190 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253062 | TAGGAGTTAGTGACT[A/G]TCTTTCTGTCACTCA | 221178 |
rs138769628 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232098 | GTGTGATTAAGGCCA[A/G]GTACCAAGATCTGCC | 221178 |
rs138789678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172762 | TTATCACAGCTGCAT[A/G]CATCTTGAAATTGGA | 221178 |
rs138798436 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004273 | AGTCATCAGTCAATA[A/C]AGAGTCAGGAGTGAA | 221178 |
rs138799997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264681 | ATCCCTGTTGTGTTC[C/T]TGTTATGTTTGAAAT | 221178 |
rs138814715 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237893 | ATCATTTATAATATA[C/T]AAACATACATGTTTA | 221178 |
rs138824840 | in-del | -/T | 0.239902 | 0.249796 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044407 | AATTTTTGTATTTTT[-/T]AGTAGAGACGGGGTT | 221178 |
rs138827975 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165189 | CACTTCCACCCATTT[A/C]CCTGAAGCGGGACTG | 221178 |
rs138835093 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231766 | CCTTGCCAGGACTTG[A/G]TATTGTCAGTATTCT | 221178 |
rs138855024 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137688 | TGCTTGAGCCTGGGG[A/G]GCGGAGGTTGCAGTG | 221178 |
rs138860891 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167831 | CTTGTCCCATCATGA[A/C]TATTCATTCTTCCTT | 221178 |
rs138861720 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127590 | AGATGACTGTGATGA[A/G]TCATTCAAGTTCAGT | 221178 |
rs138865747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066595 | GCCTCACCCATGGAG[A/G]GGACAGCAGGTGCTC | 221178 |
rs138868746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242010 | GTGAGCACAGATCGC[A/G]CTACTTACTTCAATC | 221178 |
rs138899509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097677 | AAAACAAGCCAGGCA[C/T]AGTTTCAGTGTCTGT | 221178 |
rs138907553 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159295 | ATATTTTTTCAGCTT[C/T]AAAAATACATGGTCA | 221178 |
rs138918146 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130997 | GCTTCATCGTGATTC[A/C]CTTACTTGCCTTCGT | 221178 |
rs138932298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032305 | TGCTCTCTCTCCCCT[A/G]TGGCAATACCACATA | 221178 |
rs138938793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000119 | AACCTAGTGGGAGGG[A/T]TAGATGTTGATCAAA | 221178 |
rs138946174 | snp | A/G | 4.94401e-05 | 0.00497168 | missense | SPATA13 | GRCh38.p7 | 13:24290790 | CAGATGATTGACATC[A/G]CCATCGACGGGTTCC | 221178 |
rs138946560 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215198 | TTCATTGGTGGCATC[A/C]TGTCACATGACTGTC | 221178 |
rs138948662 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149004 | CTGGGCTTGGAGGAA[C/T]GTAGGCTCCGTCCAC | 221178 |
rs138965346 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034552 | TAACAAACCAGACAA[C/T]GCTTAATAGTTTAAG | 221178 |
rs138982592 | in-del | -/AT | 0.0807149 | 0.183963 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090239 | GCATGATAAACTCAC[-/AT]GTGTTGACTTCTCTG | 221178 |
rs138983709 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080903 | AAACCACTTCCAGTG[C/T]ACCTGTCTTCTGTCC | 221178 |
rs138990369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072579 | CCTCCTGCTCACACA[C/T]AGCTCAGTCCCCAGA | 221178 |
rs139001764 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021993 | TGGGATTACAGGCGT[A/G]AGCCACTGCGCCCGG | 221178 |
rs139017000 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169829 | TCCCCACTCTCCTCT[C/G]CTGCCTGGCTGCTCT | 221178 |
rs139023895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278249 | GTGGGTAAGAGTTAG[A/G]TGGCCTGAGCCTGCT | 221178 |
rs139032621 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235989 | CAGCCACTTGTGACA[C/T]AGGTGATTTTTGTAT | 221178 |
rs139037404 | in-del | -/C | 0.421526 | 0.181876 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101497 | TGTGGTGAAAAAAAA[-/C]AACACATAAAACTTA | 221178 |
rs139042493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982867 | GTGAGCTTCGGGAGG[C/G]TGGGTCTCCCACCAG | 221178 |
rs139058790 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101727 | ATATAAGTGGAATTG[-/T]TCAGTATTTATCTCT | 221178 |
rs139059736 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017350 | TAAGCCCACGTGCTT[A/G]ACCTGAATTCAGAGG | 221178 |
rs139060641 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145177 | GTGTCAGAAAGAGAC[A/G]GTGTGAAAGGCACTT | 221178 |
rs139063276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135112 | ATGCCTTGATCTCGA[A/T]CTTCTCAACTCCAGA | 221178 |
rs139066784 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042540 | CCACCGTGGACTAAC[A/T]CACATCTCAGAGACA | 221178 |
rs139107057 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046640 | TATTAGTTCCTGTAG[A/C]TGTATAGATGTCCAA | 221178 |
rs139107153 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011339 | TGGCCATCTCATGCT[C/G]TCTCACGTTCCGCAG | 221178 |
rs139131098 | in-del | -/GGAATCCTTGGGTAAGA | 0.443598 | 0.158176 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288553 | AAAGGCGGTGCTGGT[-/GGAATCCTTGGGTAAGA]GGAATCCTTGCCCTG | 221178 |
rs139137083 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232851 | ACCACTCTCAGCCCA[A/G]TTTTATAATATTTTT | 221178 |
rs139146508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295882 | AGAAAGGTTAAATAA[C/T]TTGCCCAAGACCACA | 221178 |
rs139151784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042048 | CAGAGGCAGCCACGT[A/G]TGTCACATTTCAAGG | 221178 |
rs139170019 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194619 | TAATGAGCCCGGTAG[A/G]TCCTCATTGATTCAC | 221178 |
rs139172142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128548 | CTCAGGTAGCTTTCT[A/G]AGAATAGCCTGTCTT | 221178 |
rs139179173 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221288 | GTGTGTACTCAGTGA[C/G/T]GTTATGTTTTCCAAG | 221178 |
rs139184522 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282191 | AGTCTGGGGCTGGAC[A/G]TGTGTCTGCCGAGCA | 221178 |
rs139189340 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033310 | CAAGTCAAGAGGCAG[A/G]CATGGAGAGGCTCCT | 221178 |
rs139198866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015157 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGATG | 221178 |
rs139206531 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094684 | AGATTGCCTGAGCCC[A/G]GGAGTTTGAGGTTAC | 221178 |
rs139222310 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284375 | TTTACTAAGCATGTC[C/T]GAAAACCTGGAACTC | 221178 |
rs139230367 | snp | C/T | 0.000254194 | 0.0112709 | utr-variant-5-prime, missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24222900 | GAAGGCCTGGAGCTG[C/T]GGTCTGCGGACTCGG | 221178 |
rs139239153 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292063 | GCCCGGCCTCTCTCT[C/G]TCTTTATTATCTGCC | 221178 |
rs139258444 | snp | A/G | 0.000658718 | 0.0181363 | missense | SPATA13 | GRCh38.p7 | 13:24297502 | AGAAGGACCTGCTGC[A/G]CAGGGACATGCTGTA | 221178 |
rs139276202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119814 | CAAGACCCGGCCAGC[C/T]CCCACCGTGCATGGC | 221178 |
rs139288966 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185434 | ATCCACTTAATGAGA[A/G]ATAAACCTTTTAAGA | 221178 |
rs139293259 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227024 | TTGAGCCTGTGGAGC[A/C]GTTGTAAGGACACAG | 221178 |
rs139301526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255074 | GCCATTCAGCCAGGC[C/T]ATTAGCTCCTAACCA | 221178 |
rs139303088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059724 | AACTTTGCTGAAGTT[A/G]TTTACCAGGTGAAGA | 221178 |
rs139314900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210548 | TGGTGCCTTTGTTGA[A/C]GTTAAGTTGACCGTG | 221178 |
rs139324115 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275889 | CAGTGAGCTGAGATC[A/G]CGCCACAGCACTCCA | 221178 |
rs139340694 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111477 | CAGTGGTGCAATCAC[A/G]GCTCACTGCAGCCTC | 221178 |
rs139343052 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122508 | ATCTTCATCAATATC[A/T]TCTTCATCACTCCCC | 221178 |
rs139347637 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174363 | AATTCTTTCTTTCTT[C/G]TGCTTGCTTTAGGCT | 221178 |
rs139368253 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257849 | TTATAAATAAATAAC[A/C]TCTTGATCTGTGAAG | 221178 |
rs139389015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028121 | GACTGTTAAAATTTA[A/T]GGGCTAATACACTTA | 221178 |
rs139410793 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157620 | TCCTTTTTCTGCAGT[A/G]GAGGGTGGGGCGGAA | 221178 |
rs139443990 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301191 | TGTATTCTTAGAAAC[C/T]TTATTCCCGTCATCT | 221178 |
rs139444355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139387 | CTGTTCAGCCCACAA[A/C]AACACTTAAAAAGAA | 221178 |
rs139447497 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113863 | GACAGAGTGAGACTC[A/G]ATCTCAAAAAAAAAA | 221178 |
rs139450380 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200689 | TTTATGTTTTTTGCT[C/T]TCGGTGGTCCCCTTA | 221178 |
rs139466692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018633 | ATTGGCGAGGTGAGC[G/T]CTGCTTGTTTGATGT | 221178 |
rs139466835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293060 | TCTTACAATTAGATT[A/G]GAAAGTAAAGAATAA | 221178 |
rs139476993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102929 | AATTTTAGTTTCAGG[C/T]CTTTAACCCATTTTG | 221178 |
rs139482521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089625 | CACAAATCACCAAAA[C/T]GCCAAATAATTTTTA | 221178 |
rs139484354 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039669 | CTGTGGACTGGAGGG[G/T]TCCATAGGTTGTGAG | 221178 |
rs139484756 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029853 | ATCATTTAGCTCTCA[C/G]TTATAAGTGAGAACA | 221178 |
rs139509160 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260790 | ACTGGAAATCATAGC[A/G]GATGCATATGGGTGT | 221178 |
rs139517383 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198182 | ATATTTTTAGTAGAG[A/T]CGGGGTTTCACTGTG | 221178 |
rs139527040 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032977 | CTCATTTTGGGTAGA[C/T]TGGAAAGGTTTGTGT | 221178 |
rs139533096 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193381 | ATTGTTGACACAGGC[-/G]GGTGGCCATGTTGTT | 221178 |
rs139541678 | snp | C/T | 3.38146e-05 | 0.00411171 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24249776 | AAGGCGCCCCATTTC[C/T]GTGATAGGTGGGGTC | 221178 |
rs139549931 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093586 | TTGAAATCTGATTGG[C/T]TTGTTTCTTCTGTGC | 221178 |
rs139567754 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098898 | CACCACTGCACTCCA[C/G]CCTGGCAACAGAGCG | 221178 |
rs139567915 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260230 | TAGGGATGAAGGGAG[A/T]TAGATTAAGTTTGTT | 221178 |
rs139571252 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014011 | CCTCCAAACCCGTCA[C/G/T]GCAAAGGGGCTGTAT | 221178 |
rs139580030 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200155 | CCCAACTACAGTTTG[A/C]TGAATACTATTGTTA | 221178 |
rs139581948 | snp | C/T | 0.000343112 | 0.0130934 | intron-variant, nc-transcript-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24162451 | CTGTCACCTTGCAGA[C/T]GGCTTTCTCTCCGAA | 221178 |
rs139593585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161530 | CGGAGTTGGTTTGGT[C/T]CCATTCTGTGCAGGA | 221178 |
rs139598737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250642 | TACTGGATTGTATAC[A/G]TCTACATTTTTCCTG | 221178 |
rs139610440 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001497 | GAGTGGCGGTGGAGA[A/G]GGGAGAATGAGCTGG | 221178 |
rs139616743 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063377 | TGGGATGGCTAAATC[A/G]AGCTACTTAACATAC | 221178 |
rs139643279 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000482 | AAGGAATGACTTTCA[C/G]GGCAGATAGAGCCCT | 221178 |
rs139649249 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165838 | TTACACAGGATTCTT[A/G]GGTCAGGCCCTAGCT | 221178 |
rs139665503 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070813 | AAACTGGCACGTCTG[A/G]TTTTTTTCTGCCTTC | 221178 |
rs139669908 | snp | A/G/T | 0.00011554 | 0.00759986 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286847 | AGGCCAGCCAGAGCC[A/G/T]CCACAGACACTGTGA | 221178 |
rs139673857 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005387 | TGCTTCTTAGACCAC[A/C]GAAGCAGCTCAGGAA | 221178 |
rs139675572 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997377 | TTCCCAGGCAAACTC[C/T]GATGCTTCCTATCAC | 221178 |
rs139694695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240548 | GATGGAGTTTGTCAC[C/T]GTCATGCGGAGTTCA | 221178 |
rs139714798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191145 | AAATTAATTAATTAT[C/T]ATTTTATGTTTGTAG | 221178 |
rs139738694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200845 | CAAAAAACCCCACTC[A/G]CTCCCACAATGAAAA | 221178 |
rs139760513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141250 | GTTTAGGAGGTCAAG[A/G]TGGGAGGATCACTTG | 221178 |
rs139760867 | in-del | -/CCC | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176325 | TATGTTTTGTAAACA[-/CCC]CCCCATTAGTTTAAC | 221178 |
rs139762412 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071020 | TCTGTGTTAATGTCT[A/G]TATCTGTGTATATAT | 221178 |
rs139764171 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009249 | CAAGGAGGGCCACCC[A/T]TCTCCCATGGTCCTG | 221178 |
rs139766693 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089262 | ATGGTTTGCTGTTCG[G/T]ATGGTCATAACCCAT | 221178 |
rs139772759 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206388 | CACCAGTCAGAATGA[C/G]TGTTATCAAAAAGTC | 221178 |
rs139780615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154178 | ATATGCACACCTGAT[A/G]GTCTGGCAGTACCAC | 221178 |
rs139792445 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243827 | AGGAGAAAACTGGGG[A/G]GTTAGCTTATTGTAT | 221178 |
rs139796747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016049 | TGAGCCACAGTGACA[C/T]GTGGCATGGTTCTGA | 221178 |
rs139799626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247320 | TTGGAAAAGAACTCA[C/T]GAAGCCCATTGTTTT | 221178 |
rs139802348 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178569 | TGCCATGCATTGCTA[C/G]GAAGGTATTATTATC | 221178 |
rs139809368 | in-del | -/TTAC | 0.350546 | 0.22889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046950 | CAGAACAGGAGTTTA[-/TTAC]TTTATTACTCAAATC | 221178 |
rs139830824 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077941 | AGGCCCTGTCCCACC[C/T]CAGGCTTGATCTCAG | 221178 |
rs139832091 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056236 | ATGAAGGAATAGAAC[A/C]AAGTGTCCAGAACAG | 221178 |
rs139845544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992154 | CTCCTCAAGTCTGGG[A/T]TCTTGGTAGAAAGTG | 221178 |
rs139860818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281866 | CCTTCCTGCTTTCCC[C/T]CCGTCCTGCTTCAAG | 221178 |
rs139867880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141813 | TATTTTTTCTAATTC[A/G]TGCATCACTTCAAGG | 221178 |
rs139907377 | in-del | -/GGGTGAACCATC | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127522 | GAAGGGTGAACCATA[-/GGGTGAACCATC]GAGTGAACCAAGGAG | 221178 |
rs139912724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183380 | AGAAACATTTAACAA[C/T]GGCATCATCATGCCT | 221178 |
rs139914597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287342 | AATTTTCTAAATTTT[A/G]TATAGAGATAGGGTC | 221178 |
rs139927090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246970 | GACTTTTAGGAAAGA[C/T]AAATAGGCTTTCAGG | 221178 |
rs139947223 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291540 | CGTTCCCTACCCACC[A/G]GGGTGCCGACTCTCT | 221178 |
rs139950142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229897 | ATAGGAGAACTTGAT[A/G]GATTCAATTCCATAA | 221178 |
rs139951171 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188257 | GAGGCAGGAGAATCA[A/C/G]TTGAACCTGGGAGGC | 221178 |
rs139972830 | in-del | -/T | 0.0622301 | 0.165053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147662 | CCATGTTTAAGTCTA[-/T]TTAAGTACATTTATA | 221178 |
rs139976035 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124427 | CAGTGTCTAACATAA[C/T]AGAAGGACAAGGTGG | 221178 |
rs139979347 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145514 | AGTGAGCTGGTAACA[C/G]ATGTAATGAAAGTAC | 221178 |
rs139979619 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186685 | AGCATAACATTGTTA[C/T]GGGAACATTAATTTT | 221178 |
rs139989620 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082011 | CTGCTGTATTGGTCT[C/T]GAATGGCTGCACCAT | 221178 |
rs139999453 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239516 | CTTGGGCAACATGGC[A/G]AAACTCTGTCTCTGC | 221178 |
rs140005773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121607 | AAGAATAGATACCCA[A/G]TGGTGAGGAAGAGAC | 221178 |
rs140010981 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060270 | ATAGAGAGCCCAGAA[A/C]TACTTACAACCTGCA | 221178 |
rs140018768 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036013 | AGTAAGACCCTGTCT[-/CA]AAAAAAAAAAAAAAA | 221178 |
rs140023914 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305315 | AGTCAGGTTCAATTC[A/G]TTGCCCCTGTCAGTT | 221178 |
rs140042302 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062911 | TGGATGGCATTCTGT[C/G]GTCATGATCCTGCCA | 221178 |
rs140044143 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026854 | TGTGACCTTTGCCTC[C/T]GCCTCCCAAAGTGTT | 221178 |
rs140048767 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149631 | TGTGGTGTAGTGCAG[C/T]GTCCTGAATTTGGAG | 221178 |
rs140057018 | snp | A/G/T | 0.0126979 | 0.078662 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306260 | CTGAACCAGCATTTT[A/G/T]TCAGGTGGAAATCTC | 221178 |
rs140072710 | in-del | -/TA | 0.438105 | 0.164671 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189498 | GTGTATATATATATA[-/TA]ATATATTTAATATTG | 221178 |
rs140090728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987739 | CATCTGCAGAACTCT[C/T]TTTATTTTACACAAT | 221178 |
rs140119066 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206478 | GGGAGTATAAATTAG[C/T]TCAGCCCTTGTGGAA | 221178 |
rs140120414 | in-del | -/TTT | 0.184838 | 0.241358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211493 | CAAAGGCTTTTTCTG[-/TTT]TATCTGTTGAGATAG | 221178 |
rs140126467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051278 | ATTTCCAATCACGTT[A/G]GACATGCTGTGCCTG | 221178 |
rs140133804 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158214 | CAAAAGATCAGCAGA[C/G]AAGAAAAGAGGTCAC | 221178 |
rs140149789 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170146 | GGTCAAATCATGCTC[C/T]AGCCACTGCCTCAGT | 221178 |
rs140150778 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210061 | TTGGCCATTTGTGTG[A/T]CTTCTTTGAAAAAAT | 221178 |
rs140157528 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275465 | CGCTGATGGTCAGCA[C/T]GCAGTTTTGATGACC | 221178 |
rs140164935 | in-del | -/TAAG | 0.0799302 | 0.184463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048465 | GTAGATCTAGTAAAC[-/TAAG]TAATCAAGGATGAAG | 221178 |
rs140185471 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110900 | CCATCTCTGCGCATA[A/G]CATATTCTTGATTAT | 221178 |
rs140187737 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054893 | AATAACAGCGCTCAC[C/T]TCTTGTGATCATATG | 221178 |
rs140199049 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122004 | AACCACTTCTGGAAC[A/C]ACTGCTAGGACGAAC | 221178 |
rs140220107 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006427 | AACGGTGTCAGACAA[C/T]GACAAGACAAACATG | 221178 |
rs140220583 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297311 | CTTAAGTAGCTAGGA[C/T]TACAGCTGTGGTAGA | 221178 |
rs140232749 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213561 | TGAGCCACCATGCCC[A/G]GCCAGGGTCTTTCTT | 221178 |
rs140239620 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283495 | GTTGGCTTTGCCAAG[C/G]GTGGCTCATTTTCCC | 221178 |
rs140241126 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277369 | GAATGGCGTGAACCT[A/G]GGAGGCGGAGCTTGC | 221178 |
rs140251134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027485 | TGATTTTATTAATAT[C/T]TCCAAAGAATAAACT | 221178 |
rs140264293 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184488 | GTACAATGGAGCCAA[C/T]CAAATCACAAAGATT | 221178 |
rs140267602 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245584 | GAATTACAGTTGTTT[-/C]TTTTTTTTTTTTTTT | 221178 |
rs140274037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287626 | ATCACCAACTGACAG[A/G]TGAGATCCTGAGTCA | 221178 |
rs140275036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248501 | GGTGATGCCTCATTT[A/G]GGATCATAGACTCTT | 221178 |
rs140294021 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266696 | TAATCCTTTTACAGT[A/G]TTGCCAATAATCAAT | 221178 |
rs140298616 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189253 | GAGGCCGGTGGATCA[C/T]GACGTCAGGAGATGG | 221178 |
rs140298635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147483 | TGTGCTCCCTTCTCC[A/G]TTGGAAGTGGTGATT | 221178 |
rs140307196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250941 | TTTTCTGTACTATAA[C/T]CTAATGTAGGGAATT | 221178 |
rs140321836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087571 | TTTCCAGCTGCATAT[C/T]GATGAATGATTCCAG | 221178 |
rs140331106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151878 | AGTACTAAGCAGTAT[A/G]GATGCTTGATTAATT | 221178 |
rs140340647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166459 | TCTAGCCCTGGGGGA[C/T]GGCGTAAACAGAGGT | 221178 |
rs140354464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053425 | TCGGGTAGAAATGAT[A/C]TACGAGAAGTAAGTA | 221178 |
rs140361095 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232964 | TACAAAGATTTTCTT[C/T]TGTGTTATTTTCTGG | 221178 |
rs140363959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989399 | TGCACTCCAGCCTGG[A/G]TGACAGAGTGAGATT | 221178 |
rs140387909 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068487 | ATATTCCTTTGGGTA[C/T]GTGCCCAGTAATGAA | 221178 |
rs140395548 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117500 | ATTTCTGTATGACTT[C/T]AGTGATGTCAGTTTT | 221178 |
rs140406083 | in-del | -/A | 0.0741063 | 0.177655 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212610 | AAGAAATGAACCAGC[-/A]AGACTTTGACAGGTT | 221178 |
rs140408177 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169129 | GGGATCTCTGCGTGT[C/G]CTTGGGCCACGCTGT | 221178 |
rs140408550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272114 | CCCAGGGTTCCTGCA[C/G]CCATGGCCTTGAGCA | 221178 |
rs140430595 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052657 | TGGAAAGGATGTGAG[A/T]TTAAGGACTCTTTGG | 221178 |
rs140439693 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114836 | CCTGGCTAATTTTGT[A/G]TTTTTAGTAGAGTTG | 221178 |
rs140444872 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203045 | ATAGGTAAACGTGTG[C/T]CATGGTGGTTGGCTG | 221178 |
rs140456152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300058 | TTTGCTCTGTCCTCT[C/T]CTTCTGGGGCCTCAT | 221178 |
rs140466054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104137 | GAGAATGTCCGTGTC[A/T]GTCTGCTCACCACAT | 221178 |
rs140467795 | snp | C/T | 0.00164772 | 0.0286556 | missense | SPATA13 | GRCh38.p7 | 13:24294839 | ATCGACAAGATAGCT[C/T]GCTGGCAGGTGTCTA | 221178 |
rs140468643 | snp | A/C/T | 0.00517997 | 0.0506535 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020995 | GCACAGGGCCTAGAT[A/C/T]GAGACACTGCACTCC | 221178 |
rs140471748 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134427 | GTTTATCACAGAGGC[A/T]GATGGGTGGGGGTGC | 221178 |
rs140477407 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167888 | ATGTTGAGCAACTGC[A/G]TCGGCCCTGACACTG | 221178 |
rs140478195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071238 | CCCTAGGACTCATAG[C/T]AGACACATTGGAATG | 221178 |
rs140481145 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988944 | ATGAAACAGGAGCTT[A/T]GTCTGAGAATTAGTA | 221178 |
rs140514723 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301936 | GGTACTGTAATCCCC[A/G]TTTTAGGGATTGGGG | 221178 |
rs140515823 | snp | A/G | 0.00505409 | 0.050015 | missense | SPATA13 | GRCh38.p7 | 13:24284267 | AGCAGCTGGCCATCA[A/G]TGAGGTACTGGAATT | 221178 |
rs140516562 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202521 | CTTTCTTTCTTTCCC[-/TT]TTTTTTTTTTTTTTT | 221178 |
rs140517973 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049351 | TGTTACAGCTGCCTA[-/C]AGTACTCAGTACAGT | 221178 |
rs140518640 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992614 | TCCCATGTATGATGA[G/T]GTCTGAAGGGTCAAT | 221178 |
rs140520448 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268961 | GATAAGAGAAGCCTA[C/T]GATATAGTATATAGT | 221178 |
rs140545971 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036879 | CTCCTGGGTTCAAGC[A/G]ATTCTCCGACCTCAG | 221178 |
rs140547550 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262885 | GAGCACTTGGAGTCT[A/G]TATGGAATAATATAC | 221178 |
rs140572559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016317 | GCTCTTCCTGAGGCT[G/T]GGAGAGCTGTTTCCC | 221178 |
rs140584399 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164087 | CACCAAATGTACATG[C/G]TTTTCTTGAGGGAAA | 221178 |
rs140585671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251326 | GGCCGGGTTTGTGGC[C/G]TTGTCCTGGCTTCCT | 221178 |
rs140585800 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038954 | GGCAATGGGCCAGAC[A/G]GGCAGCCCTGTGACA | 221178 |
rs140604374 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24099420 | AAAATGTTAGTTCCT[C/T]AGTCTCAGTGGCCAC | 221178 |
rs140607952 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065865 | TGGGCTCTGAAGTCC[A/G]AATACTTGGGTTTGA | 221178 |
rs140608184 | in-del | -/GT | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304847 | GTGGCATGTGTGGGG[-/GT]GTGTGTGTGTATGTT | 221178 |
rs140622242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131722 | GGAAATAGGAGTTTT[G/T]CTGAAGGATAGGGAC | 221178 |
rs140638468 | snp | A/G | 0.0159678 | 0.0879145 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24302707 | GGTCTTTGGCCTGGC[A/G]GAACCCAAGAGGAAG | 221178 |
rs140661147 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198468 | AGAGTCTAGAGGTCT[C/T]CAAAACCCTTTGCCA | 221178 |
rs140666816 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063846 | CTGCCTCACTCACAG[-/G]GGATGAGGGCACTCC | 221178 |
rs140686475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139752 | ATCTGCTTAATTGAT[A/G]TACCTGTTTTTGTTT | 221178 |
rs140686786 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099749 | CAAAAACTCCAGATT[C/G]AGGGAATGTGCAGAT | 221178 |
rs140689699 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037621 | CACCATGTTGGCCAC[A/G]GTGGTCTCAATCTCC | 221178 |
rs140708666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002991 | AATTGCCATCATTTG[C/T]TCTTCTTCTGTTAAT | 221178 |
rs140709413 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039771 | CTGTAGTTGGCTTTG[A/T]GCATTGTTTTGTGTA | 221178 |
rs140720484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103329 | TGTTTGTCCTATCAT[A/G]TACAGTATAGGCTGG | 221178 |
rs140746466 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280707 | CGTGGTCTGGGCAGC[C/T]GCTCCAGGGTTAGAG | 221178 |
rs140754933 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191790 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGACC | 221178 |
rs140756797 | in-del | -/CCTGCCCA | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296885 | AATAACCTTTGAGGC[-/CCTGCCCA]CCTGTGAATGGGGAC | 221178 |
rs140760555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149822 | ATGCAAAGAAACTTG[A/G]ACTCGGTTGTGTGGG | 221178 |
rs140762041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255518 | CAGATGACCAAGCTG[A/G]CCCTGCTGTGTGGTA | 221178 |
rs140766280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005824 | TTTTTGTCAATGGAG[A/G]AGTGGATTCCTTTTT | 221178 |
rs140770967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216829 | GCCAAGGTGGGAGGA[C/T]GATTTGAGGTCAGGA | 221178 |
rs140779418 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091672 | ACAAAGTAGCTAAGC[A/G]TGGTGGTGTGCACCT | 221178 |
rs140783597 | in-del | -/TCTC | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152834 | GTCTTGAAGCAGCTT[-/TCTC]TCTCTCTCTCTTTCT | 221178 |
rs140812247 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057871 | ACTCCAGATTCCCCT[C/T]CTCTCTTTTGATTTC | 221178 |
rs140815722 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993464 | ATTTACGGCAATAAG[G/T]CTTCTCTGCAAATAA | 221178 |
rs140822838 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207362 | CACATCCCGCACATG[C/T]ACCCCTGAACTTAAA | 221178 |
rs140836876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219839 | TAATTTTACTAATTT[A/G]TCGCACTGAGCTTTC | 221178 |
rs140845094 | in-del | -/G | 0.280785 | 0.248097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282581 | TGATGCCATTTCCTC[-/G]GGCAGCTCTTGTTGC | 221178 |
rs140856245 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218195 | CAGCAGAGTGAAGGA[C/T]GGGTGGGCAGTGAGC | 221178 |
rs140868384 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280301 | TTCAATAGACTCCTG[G/T]TAATTGTGAATTTAT | 221178 |
rs140885778 | in-del | -/G | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045770 | ACAGGCTGAGCCACA[-/G]GGTTGCTGGGATTTG | 221178 |
rs140887785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116613 | TTTTACAGATGAAAC[A/G]TCTCAGAGGGTAATG | 221178 |
rs140895154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150956 | CATGGCCCAGCCAAA[C/T]TGATGCATAAAGTTA | 221178 |
rs140906951 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306982 | AGTTTTTTGTAAAAA[A/G]AAATTATTTACAATG | 221178 |
rs140909163 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023047 | TGCATCCTTCAACCC[A/G]TCATTTACATTAGGT | 221178 |
rs140918016 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082535 | AAATAAAAATAAGAT[A/C]TTTGGCCGGGCGCGG | 221178 |
rs140928194 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175840 | AACTTTAGAAATCCC[-/C]AGTGGCTTCTATGCA | 221178 |
rs140931073 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022199 | AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 221178 |
rs140933786 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283236 | TCCCTATTATATTTC[C/T]ACTTCCTGGCTGCAG | 221178 |
rs140934526 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171353 | TCAGATCTGACAACA[A/C]CTGCTGCTTCCATGG | 221178 |
rs140940104 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221557 | TGGACACAGATGTGC[A/G]TGATGGGGAAAGCAT | 221178 |
rs140952285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081301 | GTTCACCGGTAATCT[A/G]TATGAGGCCCTTCTC | 221178 |
rs140957136 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985039 | AATGCTCACCTCAGA[C/T]GCACCCTCCTCAAAT | 221178 |
rs140992136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118556 | GGTGGTTTATTAAAA[C/T]ACAGATGACTTAAGC | 221178 |
rs141005897 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184017 | CACAGGAAGTGGCGC[A/G]CTCAAGGTCACCCAG | 221178 |
rs141014127 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084305 | GTCTCTGTGCTTGCA[A/G]TTCTGCTTCTTTTGA | 221178 |
rs141018375 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983376 | AGAGCCCACCCATAT[A/G]ACCTCATTATACCTC | 221178 |
rs141020387 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025992 | GTATTTTTAATAGAG[A/G]TGGGGTTTCACCATG | 221178 |
rs141026936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079206 | GTAGATGGCCCACAT[A/G]GCTGCAGGAGAGACT | 221178 |
rs141038148 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233691 | CTAATTCTTTTTCAA[C/T]GGAAAGTTTCAAAGT | 221178 |
rs141049465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298360 | TCAGGATGCCGCATC[A/G]TCCATTGCAGTTAAG | 221178 |
rs141050341 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978181 | AGTGCTGGGATTACA[A/G]GCGTGAGCTACTGGG | 221178 |
rs141056282 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261407 | CAGCTCGATGAAGAT[G/T]ACATCACCATATCCT | 221178 |
rs141058350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986949 | ACCATTTTACATTAT[A/G]GGAAATTTGACAAGT | 221178 |
rs141058942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082997 | TGCTTCTGACTATAA[A/G]TCTAAATGTTTAATG | 221178 |
rs141058998 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023329 | AATCTTCTGTGAAAG[C/T]TGTAGACATTAAGGC | 221178 |
rs141059253 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121923 | GTTGCATGATCGGGT[C/T]CCATCTCCTGGGGTT | 221178 |
rs141068152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043094 | GTTTCAGGTGTTGGC[A/G]AGGTCACATCTCTCC | 221178 |
rs141072437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196926 | ACAGTTTGAAGAGGA[A/G]AAAGAGATGAATGTG | 221178 |
rs141081431 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283964 | TTAATGTCACACTTA[A/T]CTGCAGCTCTTAACT | 221178 |
rs141098280 | in-del | -/TTTTC | 0.0166523 | 0.0897153 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041615 | GATGTTAAGGAAATG[-/TTTTC]TTTTCATTCTTTTTC | 221178 |
rs141099205 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097065 | AAACAGCGTTGGCCC[C/T]GGCTGAAACGGTGCC | 221178 |
rs141102340 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196276 | TAAGAGTGAGGCTTG[A/G]CATAAACCCTTCACA | 221178 |
rs141105383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034251 | TCAAACCTCAGGGAA[A/C]CTTCTTTGTATAACC | 221178 |
rs141121040 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085578 | GACCCTAGATCCAGA[A/G]GAAGGTGCTCCTTCT | 221178 |
rs141137339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116102 | AGACCATTCAGGCTG[C/T]TATGACAGAACACCA | 221178 |
rs141142575 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054664 | AAGAGAAAATATGTG[A/G]AATATAATAATAGTA | 221178 |
rs141153539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270269 | GAACTTACATGTATA[C/T]CTTTACATGTATGCC | 221178 |
rs141153848 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205830 | CCAAAAACAAGCAAT[A/G]GAGAAAGGATACCCT | 221178 |
rs141165705 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021967 | CTGCCTGCCTCGGCC[C/T]CCCAAAGTGCTGGGA | 221178 |
rs141190231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169275 | TGTGCTTGTTATACC[A/G]GGCTGATGTGGAGTG | 221178 |
rs141211227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999467 | TATTAACAATATTGA[A/G]TCTTCCAACCCATCA | 221178 |
rs141216843 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24205022 | GATTCCCCTTGAAAA[-/C]CCGACACAAGACAAG | 221178 |
rs141230211 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302295 | TAAGAATTAGCTCTC[G/T]ACAAAAAAATATAAA | 221178 |
rs141247175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113084 | ACTGAGGGACTTCTC[A/G]GCTCTCTTTCCTAAA | 221178 |
rs141255586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175811 | GGTGTCATTTTTCTT[C/T]TCCCACAGGAGAGAA | 221178 |
rs141259642 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24265366 | CATCACTGTGACCTG[C/T]AGATTAATAATCATG | 221178 |
rs141274374 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198744 | GTGAGGGCTATCCCA[C/T]GTGCTGCCACGAGGA | 221178 |
rs141279079 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24264327 | AGGAGAGCAAGACAG[C/T]TAAATGTCTAGCGAA | 221178 |
rs141293306 | snp | C/T | 0.000692007 | 0.0185883 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290675 | CTTTGCCATCTATTC[C/T]GAGTACTGCAACAAC | 221178 |
rs141303832 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063926 | ATGACCTGAGGTCTT[C/T]GTTCCCTGCCTGCCT | 221178 |
rs141303940 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002039 | GCACTGTGAGCCACA[C/T]GTCAACATCTTACAT | 221178 |
rs141304625 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164735 | CCACCTGCATCCCTC[A/G]GTGTGTCTGTCTTCC | 221178 |
rs141304845 | in-del | -/AAAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098620 | AGAAGAAAAGAAAGA[-/AAAG]AAGAAAGAAAAAAGA | 221178 |
rs141307394 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201924 | TAGTTTTGCCTTTTC[C/T]AGAATGTCATGTAGT | 221178 |
rs141309165 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232157 | GATGTGTAGTTCAGC[A/G]TGAGCCTGGAAGCCT | 221178 |
rs141311612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268484 | CTGTAAGAGGCTGGG[C/T]GCAGTGGCTCATGCC | 221178 |
rs141312904 | snp | A/C/G | 0.000325699 | 0.0127573 | missense | SPATA13 | GRCh38.p7 | 13:24297727 | GGGTGCAAGAGGACA[A/C/G]GGAGATGGGTGAGCA | 221178 |
rs141337500 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167463 | TGCCAACAGAGAACA[C/T]GGGGCCCACAGGCCA | 221178 |
rs141342187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242173 | GGTTCCATAGACGGC[A/C]AGTTAGGGGAAGAGG | 221178 |
rs141371221 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067552 | TGATAGAGCTGTAAT[A/G]AATATCAAATTTAAA | 221178 |
rs141374781 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106672 | CTGGTTCTGGGGCCG[A/C]CAGAGCTGGCTCTCG | 221178 |
rs141380641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128301 | GGACATTGTGGCTTC[A/G]TCACCAGAAATGCTC | 221178 |
rs141408650 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012708 | TGCAAGCCTGTGATT[A/T]CAGCACCTGCCTTGC | 221178 |
rs141409560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244895 | GCAGAGAAGCAAGAG[G/T]TAAAAGGGCAGCAAT | 221178 |
rs141451594 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256936 | AAGGATGCCCACACT[A/G]CTAGAAGATTTTCCT | 221178 |
rs141452735 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193401 | GCCATGTTGTTTGTA[C/T]TGGGGGCCTGGTGAG | 221178 |
rs141460404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143412 | GGGGAAGGCATTAGA[A/G]TAGAGGTTTTGTGTT | 221178 |
rs141470068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070307 | GCGTGGCTGACCAGG[A/G]CTGCAGCATTTCTCT | 221178 |
rs141470751 | in-del | -/TTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025814 | TTCTTTCTTTCTTTC[-/TTTTT]TTTTTTTTTGAGACG | 221178 |
rs141472722 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207073 | TCCTTTGCAGTTATA[C/T]GGATGGAGTTGGAAG | 221178 |
rs141475169 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008170 | ACACTGTGTGCCCTC[A/G]GGTCATTTATTGCAC | 221178 |
rs141478961 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093403 | ATTTTTAAAAGAGGA[C/T]GTATGGTTAGTGATC | 221178 |
rs141487299 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157078 | TTGCCTCTGCTTCCC[C/T]AACCCGGTCTAGACC | 221178 |
rs141494341 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246827 | GAGATCACACCACTG[C/T]ACTCCAGCCTGGTGA | 221178 |
rs141499395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995862 | GGCTGCCTTGAACTG[C/T]GTGGAGGAAGTGGTC | 221178 |
rs141512439 | in-del | -/TTTTTAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110918 | ATTCTTGATTATCTC[-/TTTTTAT]TTTTTATTTTTTATT | 221178 |
rs141520364 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179296 | GGGCATATACCTATG[C/T]GTGGCATTGCTGAGT | 221178 |
rs141520477 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140024 | CAGTGAGCCAAGGTC[A/G]TGCCACTGCACGCCA | 221178 |
rs141521585 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182056 | AAAAAGTTGTGTTGG[A/C]ATTATTAAACTACTT | 221178 |
rs141521750 | snp | C/G/T | 0.00279242 | 0.0372774 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140764 | TGAATTCTGGGTTTT[C/G/T]TAACTTCATTAGTGA | 221178 |
rs141531596 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076697 | AGGTGCAAGGACAGG[A/G]AAGGAAGGAAGGATC | 221178 |
rs141541689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244480 | ACTGGAGGTAACATA[A/G]CCTATATTGGCTTTT | 221178 |
rs141571204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080443 | TCACATGCATCATCA[C/T]TCAAAATGAATAAAA | 221178 |
rs141583968 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153025 | AAAGCAGTGTTGTGC[A/G]TGTGTGTGAGAAAAA | 221178 |
rs141584663 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142932 | TCCTTTCTTGCAGGG[C/T]TGAAGCAGCTCTCCA | 221178 |
rs141590262 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218744 | TTTTTAATCTCATCA[A/G]CAGTTGTGTTAGTGT | 221178 |
rs141594325 | in-del | -/GCACCATC | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161164 | CCTCTGGGCCACCCG[-/GCACCATC]GCTTTTGGGAGGACA | 221178 |
rs141596550 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079552 | TCAGCTGATGATCCC[A/G]ACCTGAGACTAGGCA | 221178 |
rs141604341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000026 | TGAAAAATAGTGCTT[C/G]CCCTCATTAGTTATC | 221178 |
rs141618936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084169 | TTCCGTAACTTAGCA[A/G]CAAGCGAGACGAGAG | 221178 |
rs141623809 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173064 | TTTTTTTGAGTCATT[A/G]CAAAGTGGTATTATG | 221178 |
rs141627385 | snp | A/G | 0.0205511 | 0.0992634 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979546 | CCTGCTCCGGGCTCA[A/G]CCCGGGCCCCCCACC | 221178 |
rs141628760 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148951 | GCTCTCCTATGCATG[C/T]CACATGAGAGCAGGG | 221178 |
rs141630856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238866 | TTTGGCAGCAGAACA[C/T]ATTAGATTCTTGTAT | 221178 |
rs141638971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083833 | TAACTGCTCATTTCC[C/T]GGCTGCTCCTTCCCT | 221178 |
rs141646653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050508 | AGCTTAGGGGCCACT[A/G]TCCCTGGTCAGGCAC | 221178 |
rs141653590 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982281 | CTGCATGAAGACTTT[A/G]CTATGCATTTTCCAC | 221178 |
rs141654851 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986635 | AGTCTGCCTGGGAAA[A/C]TGTTTAGAGGTGTGG | 221178 |
rs141660758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043807 | CACACACTGAGATTT[C/T]CTATTAAATACCCTT | 221178 |
rs141663649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045453 | TGCTGCGACATGAAA[A/C]CATCAAATGCCCTAA | 221178 |
rs141690505 | in-del | -/C | 0.211819 | 0.247067 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054558 | TTTAGTTTAAATTAA[-/C]TTTGACATGTAGCAG | 221178 |
rs141693449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985918 | CACACAGGGACGAGG[A/G]AGCCAGCCTGGGTAC | 221178 |
rs141700551 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047786 | GATATATGGAAAGAG[A/G]CTTATGATGAGGGAC | 221178 |
rs141718084 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983684 | AGAACTGAATTCTAT[A/G]TCTAGCTTGCTTCAT | 221178 |
rs141723698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144227 | GTCAGGACTTGGATC[C/T]AGTCTGTCCAATGCT | 221178 |
rs141741062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235508 | CTCATGCCTATAATC[C/T]CAGCACTTTGGGAGG | 221178 |
rs141744163 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227498 | AGTTTATTAAAGGTG[C/T]GTGCACATGTTGATA | 221178 |
rs141745793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300606 | TTAGAACTCAAGGGC[A/C]GGTCCAGAACAGGGG | 221178 |
rs141750242 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289977 | TGTTAAGTTAGTCAG[C/T]TGGAGGCTGGGCCCC | 221178 |
rs141763867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134318 | CATGAAAAGTGTAAG[C/T]CCTGGCCCCCTTCCC | 221178 |
rs141771237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291548 | ACCCACCGGGGTGCC[A/G]ACTCTCTGGTCTTCT | 221178 |
rs141773173 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198069 | GGCATGATCTCTGCT[C/T]ACTGCAACCTCCACC | 221178 |
rs141795462 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098048 | GCTAATTATTTCACA[C/T]GAAAATGGCCCTAGA | 221178 |
rs141796310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013885 | TCATGTTGTTCATGA[G/T]GTTATTGGGAGCAGG | 221178 |
rs141807925 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231304 | AGAGCTATTTTTTGT[C/G]TCTATTATTTTACTT | 221178 |
rs141818208 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294151 | GAGCGGGGCCCTCCT[C/G]GGGAGAACATTTTAG | 221178 |
rs141837297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295464 | AAAAGTAAAAAAAAT[C/T]AGCCAGGCATGGTGG | 221178 |
rs141863860 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072424 | TCGCATTGAGCCTGA[A/G]GCAGGTGGATCTTCA | 221178 |
rs141878113 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228580 | TGGGAAACAAAATAC[A/G]AACTAAGGGAAACAA | 221178 |
rs141884333 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290454 | GCTGAAGCACCCCTT[A/C/G]TCGCCGGCCAGATAA | 221178 |
rs141902900 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257218 | GTCCAGAGTTCAGAT[G/T]AGCTTGCTTTTCTTA | 221178 |
rs141909591 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190510 | AGGAGGAGGTAAAAA[G/T]ACCACCCTTAACAGG | 221178 |
rs141925569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061221 | GAACTGTCAAAAATA[A/G]CAGCTTCTTGCAAGG | 221178 |
rs141933529 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089077 | CAATTGGCAGTTTTC[A/T]TAGATGAGGACACCA | 221178 |
rs141933654 | in-del | -/G | 0.0944967 | 0.195752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096695 | AGAAATTAGACATGA[-/G]GGGGAGTCACCTAAG | 221178 |
rs141939176 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122196 | GATCAGCCAGCATTG[C/T]TATATACTGTAACTG | 221178 |
rs141939260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163050 | CTGTCACCTCATCCA[C/T]GCTATCAGTCTACTT | 221178 |
rs141939652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029066 | TATTTATTCAAAACC[G/T]TTATTTTTAATTATC | 221178 |
rs141951800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124065 | ACACACAGAAAGCAA[C/T]GGGATTTGTCAGAAT | 221178 |
rs141953719 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165265 | GGGATTCTGTGCCTG[C/T]CTCAGACTGTCTCCC | 221178 |
rs141958157 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231063 | ACACTTGGCTCCCCC[A/C/G]AGAAGGCTTCCCCAC | 221178 |
rs141966424 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231962 | GCATTCTTTGTCATC[C/T]TTTTATTGAGCAGTT | 221178 |
rs141990079 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067078 | TTGCATTTCTTTCTG[G/T]TCCCTCTTGGCTAGG | 221178 |
rs141999313 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127612 | AAGTTCAGTTTAGAG[A/C]CTTCCAGCCCATAGC | 221178 |
rs142001467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125506 | ATCCCTTCAGGGGTC[A/G]TATGGACCAACCTAA | 221178 |
rs142023561 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249379 | TAAATCAAGAAAACC[C/T]GAGGCACGGCTGTGG | 221178 |
rs142028306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185108 | TTCGGGCATTTCCCC[C/T]GCTTTCTGTAGCTCC | 221178 |
rs142036251 | in-del | -/AAAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999369 | AAAAAAAAAAAAAAA[-/AAAAA]AAAAGCCTGTTCGGA | 221178 |
rs142050248 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030563 | ATTAAAGCCCCAGCC[C/G]CAGAGCCTAGAGCTT | 221178 |
rs142058449 | in-del | -/TGTC | 0.217851 | 0.247924 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024454 | CTCATTCTCTTGGGT[-/TGTC]TGTCTAGTGACAAGA | 221178 |
rs142059718 | in-del | -/C | 0.0528381 | 0.153711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200494 | TCCTTGAATGTCCCA[-/C]CCTCGTTCTCAGCCC | 221178 |
rs142063518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032415 | TCTTCTTAAACAGTC[C/G]ACATGGTATTATTCT | 221178 |
rs142090862 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105283 | GCACACCATCATGCC[A/G]GGCTAATTTTTATTT | 221178 |
rs142102973 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258307 | AAAAGTGTCACAGAT[A/G]TGTGAAATTGGTCCT | 221178 |
rs142103406 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034728 | GTACGGCACCTACAC[A/G]TGGCTGCTTGTATGG | 221178 |
rs142122852 | in-del | -/AAC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052377 | GATCCCATCGCTACA[-/AAC]AACAAGAACAACAAC | 221178 |
rs142123659 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071448 | CTTTAACTCTCATAA[C/G]AACTCTGTGAAGTGG | 221178 |
rs142125764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010211 | TTATATGTGAGAGGG[C/G]ATAGTAGTCGCTTCT | 221178 |
rs142143439 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033713 | GGGGGAGATTGCGTA[A/G]TGTGCTGATGGAGCA | 221178 |
rs142163164 | in-del | -/AG | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104381 | GCCCACTCAATTTTT[-/AG]AGAGGTTTGGTTTTA | 221178 |
rs142212686 | in-del | -/AGATGAAGTAT | 0.314301 | 0.241589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024282 | AGGACTTTGAATGAA[-/AGATGAAGTAT]AGATGAAGTATAGAG | 221178 |
rs142225816 | in-del | -/GAAAGAACAGGCA | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252553 | ATGGCAGAAGATTTT[-/GAAAGAACAGGCA]GAAATAACAGTAGCA | 221178 |
rs142228427 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278295 | TTATTGGGACTTGAG[C/T]TTCCTCATCTGCAAG | 221178 |
rs142231073 | snp | C/T | 0.000559706 | 0.0167194 | missense | SPATA13 | GRCh38.p7 | 13:24297367 | CATCCTTCCAGGGAC[C/T]GGATATCTTAGACCG | 221178 |
rs142237257 | snp | C/T | 0.319376 | 0.240181 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213411 | AGCTGGGACTACAGG[C/T]GTGGGCCACCATGCC | 221178 |
rs142244461 | snp | A/C/G | 0.000103281 | 0.00718539 | missense | SPATA13 | GRCh38.p7 | 13:24286388 | TTCCCCGCGAGCTTC[A/C/G]TCAGAGTAAGTGTGG | 221178 |
rs142246103 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220876 | GAACATGGGGCGTAG[A/G]AGCAGAAGAGAGATG | 221178 |
rs142261154 | snp | A/G | 4.96348e-05 | 0.00498146 | missense | SPATA13 | GRCh38.p7 | 13:24251827 | CCATTGGGTTGGACC[A/G]TGTGGGACGCCGGCG | 221178 |
rs142271500 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085497 | GTGCCGTCTGGAAGC[C/T]CTGCCCTGTGGGGAC | 221178 |
rs142274549 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177463 | GTGAAGGGGGCAAGG[C/G]TGTCTCTCTTAGGCC | 221178 |
rs142278174 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149902 | AGCAGGAGGTGGTTG[G/T]GGAGGAACACAGAGA | 221178 |
rs142283967 | snp | C/T | 0.00286056 | 0.0377107 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290852 | CCCGCTGCAGCTGGC[C/T]GAGCTGCTCAAGTAT | 221178 |
rs142284516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241054 | CATGTCACCCCATTC[C/T]GTAGTAATTAGAAAA | 221178 |
rs142290220 | snp | C/T | 0.0349115 | 0.127424 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306445 | AGAAGTATGAATAAA[C/T]GTCCTTTCACCAGCT | 221178 |
rs142290688 | in-del | -/CATA | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220385 | TCAGTGCGAGTCATA[-/CATA]AGAAGACCATTACTA | 221178 |
rs142291196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988395 | ATGGTATTCTGTGCT[A/G]TGGTGATAACATATT | 221178 |
rs142292795 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175069 | GTTTGTATGGCCCGG[A/G]GTATTGGTCCATCTT | 221178 |
rs142293466 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243435 | AGGAACATCTGCAAA[C/G]TTCTGTTTTCCTTCT | 221178 |
rs142300800 | snp | A/G | 4.98434e-05 | 0.00499192 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286928 | AGCGGGTGTACATCA[A/G]ACACCTCAGGGACAT | 221178 |
rs142308097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241674 | TATGGGGCACCTCCC[C/T]GCGTGCCGGGATAAT | 221178 |
rs142332296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108216 | CCTCGTGATTTAATC[A/G]CCGCCTAAAGGCTCC | 221178 |
rs142333274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145789 | AGGAGGGCGTGAAGG[A/G]GACTAAGACAGGAAA | 221178 |
rs142339402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211585 | TTTATTTAGTAAGGT[A/G]CATCTCCGTTGGACC | 221178 |
rs142343700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214465 | CAATGCATGTGCTTC[C/T]CTAAAAGTAAAAGAA | 221178 |
rs142349900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110873 | CCTGCTAAAGACTGA[A/C]ATATGTTTGCACCAT | 221178 |
rs142375445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111891 | ACTCATAATCTCCCC[A/G]TTTATGTTTCCTTGT | 221178 |
rs142377515 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049122 | GATGAGGAGCCTAGA[A/C]CAAGTGTATTGATTC | 221178 |
rs142408229 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177055 | CAGGCACGAGCTGCC[A/G]CACCCAGCCTGTAGT | 221178 |
rs142412917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301827 | TAAAAATACCTATGC[C/T]GGTGAAGTTTTGATT | 221178 |
rs142418222 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017056 | AGTGTGGGAGGAGGT[G/T]ACAGGGTCAGGGGGC | 221178 |
rs142424373 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059333 | GTCACAAAAAAAAAA[-/A]GGCTTGTCTTTGATC | 221178 |
rs142438148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047159 | CATGAGTCACGGGTC[A/G]GGTGCAGTCATTCAT | 221178 |
rs142447773 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198200 | GGGTTTCACTGTGTT[A/G]GCCAGGCTGGTCTTG | 221178 |
rs142477684 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018541 | TTTAGATAATTTAAT[G/T]TGAGATTATGTTTAG | 221178 |
rs142477897 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115964 | TGACTCAGGAGAGGA[C/G]AAGGTGAGAGCCACA | 221178 |
rs142479818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077583 | TACACAAGATACCCC[A/G]TAACAAACATGCACA | 221178 |
rs142483385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163409 | ACTCTGTCTCTAAAA[A/C]AATTAAGTTAAATTA | 221178 |
rs142488789 | in-del | -/GTGTGCCTGCATGTGTGCACATGCGC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114358 | ATTCAGTGTGCACGT[-/GTGTGCCTGCATGTGTGCACATGCGC]GTGTGCCTGCATGTG | 221178 |
rs142510724 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020786 | AGATGACTCATGCCT[A/G]TAATTCCAGCACTTT | 221178 |
rs142538593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138265 | TAAGCTGGGATGCAC[C/T]ATTCCAGTCCAGCCC | 221178 |
rs142542427 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074102 | ATGTTAAGTGCATTC[A/G]CATTTGTACATCCAA | 221178 |
rs142543974 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080365 | GAATAAGCAGGAACC[A/T]ACGACTTACTAGAAA | 221178 |
rs142545163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256729 | GCCACACAGCCTGCG[A/G]AGGCAGGTCATGTGG | 221178 |
rs142552809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292185 | GCCAACCATCATTTC[A/G]TGCATGCACAGAAGC | 221178 |
rs142556186 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230536 | AGGCAGATGCCCACA[G/T]CTGAGCTCAGCTCTG | 221178 |
rs142564453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039452 | TCACAAGTTTAATCT[G/T]TAGAATGTGCAGAAT | 221178 |
rs142579144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125318 | AGAGTAGGGAAACTT[C/G]CTGTCATTCCTAATG | 221178 |
rs142582108 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257887 | CATGACCCAAATTTT[A/G]TGCCAACCAGCCTGT | 221178 |
rs142586696 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191697 | TTGTATTTTTAGTAG[A/G]GACAGGGTTTCACTG | 221178 |
rs142612025 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258673 | ACCTCCTCTCCGCTA[A/C]AAAAAAAGAGAGACT | 221178 |
rs142613553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091442 | ATTAATAGTGTTTGA[C/T]AAATGCCTTTGAGAT | 221178 |
rs142648334 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260168 | CATGTCAGTCGGATC[G/T]GGGCTGTCCCAAGCC | 221178 |
rs142652845 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158884 | CGGGGGTCTTCAGGT[A/C]TAGTTGGTATCACTC | 221178 |
rs142663038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226775 | AAGCCAGGACAGCCT[C/G]TGCACTGTCCATCTT | 221178 |
rs142672745 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991033 | AAGAAGATGAAGCCC[A/G]CTCAAGGTTAAGATC | 221178 |
rs142707070 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264732 | GAAAATAACCAGGTA[A/G]ATACAGAAAAGAAGT | 221178 |
rs142716261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036592 | GGAGACACCCAGGGA[C/T]GAGATCTCTCTGAGC | 221178 |
rs142722095 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993628 | TCCCACAGACCCCTG[C/T]GTGACATTGTTGGAC | 221178 |
rs142731787 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250458 | ATTAAAGACCCTATC[G/T]TGGAGAAGTGTATAC | 221178 |
rs142734171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235798 | ATATGTTGAGCAGTG[C/T]AAGTCTAGCAATTGC | 221178 |
rs142739512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300969 | GACAAAAAAAGACAC[A/G]TGAGCTGATTTAGGG | 221178 |
rs142741276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187578 | TACAATAGCATGTGC[A/G]TACATCTTGTCTGTT | 221178 |
rs142743167 | in-del | -/TGA | 0.411242 | 0.191052 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996616 | CCACCTGTGCTTGGC[-/TGA]TGATTGGCTGAGATT | 221178 |
rs142758522 | snp | A/C/G | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197576 | TTCTGAAAGATAGAA[A/C/G]TAATTTGCATCTCTA | 221178 |
rs142774286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259698 | GATGAGCTTAAAATT[A/C]TTGGGAAATGCTATA | 221178 |
rs142786986 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117366 | CTGGCTCTGTAACCT[A/G]GTTATCCTTGTCTTT | 221178 |
rs142788668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033145 | CCCCAGACCTGCAAG[A/G]TTTGAGTATCATTTG | 221178 |
rs142811399 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271885 | ACAGACAGAAAGCAG[A/G]GATGTGGTTACGGCT | 221178 |
rs142816683 | snp | A/C | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160168 | CAGTGGGCAGTGGGG[A/C]ACGGTTGCCCCGGAG | 221178 |
rs142823327 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039215 | AGAAACACTGTCTTG[A/C]TTGTTCCACTTTTAA | 221178 |
rs142826913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097862 | ACACTCAGGAGAAAC[C/T]GCGGAGAACAGAATC | 221178 |
rs142832151 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022768 | CCATGTTGTTTTCAC[C/T]GATGACTACTTCTGC | 221178 |
rs142839570 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017065 | GGAGGTGACAGGGTC[-/A]GGGGGCAGACATCCT | 221178 |
rs142847116 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140055 | GCCTGGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 221178 |
rs142848991 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101866 | GTTTACCACATGTTC[G/T]TTGCCCATTGGTCCA | 221178 |
rs142861686 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203787 | GAATTTTTGTAGTCT[C/G]TCCCACAGAAGGATA | 221178 |
rs142868820 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000631 | GAAGGATTCTCAGGA[A/T]AGGGCAACAGGACAT | 221178 |
rs142878602 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062518 | GTGAACCTGGGTCAC[C/T]TCACCTCCATGGAGC | 221178 |
rs142878764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100246 | TTTACTGAACCTTTT[C/T]ACCAAGTGGCACCTA | 221178 |
rs142890917 | in-del | -/CAGGGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052826 | ACTTCCCCCTGCCGC[-/CAGGGG]ATCCTCCCCGCCACT | 221178 |
rs142906131 | snp | C/T | 0.00170086 | 0.0291125 | missense | SPATA13 | GRCh38.p7 | 13:24286349 | GACTGGTGGTGGGGC[C/T]GCAGTGAAGATAAGG | 221178 |
rs142911784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003978 | CACTTGCTTCATATA[A/C]ATACACACAGAAACA | 221178 |
rs142914905 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041118 | TTGTGGGATGGGGGT[A/G]GGATGTGGCTGAAAT | 221178 |
rs142915252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104306 | ACAAAAAGGATTTTA[C/T]TTCATCTTAATTTAA | 221178 |
rs142919354 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103541 | GAGAGAGAGAGAGAG[A/T]GAAGAGAGAGAGAGA | 221178 |
rs142920632 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114469 | CAGGAAAGAGAGCTG[G/T]CCAGCACACACTTGG | 221178 |
rs142929075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178529 | AGTAGTAGTAATAAG[C/T]ACCCTAATAAATGAG | 221178 |
rs142935809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267772 | TTCATTCTGACTAAA[C/T]TCAAGCCCACCCATT | 221178 |
rs142936904 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991958 | ACACGGTGATGAAGA[A/T]CATGGGGTTATTGTA | 221178 |
rs142942793 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066108 | TGAATTGTTAAAGGT[A/G]CATACCTATATTGTA | 221178 |
rs142951630 | in-del | -/TTGTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105121 | TACAATCGTTTTGTT[-/TTGTT]TTGTTTTGTTTCTGT | 221178 |
rs142952545 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24078737 | TCAATAGCCCATCAG[C/T]GTACATTCACCTTCC | 221178 |
rs142955628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167413 | CACAGCTAATTCTGT[A/G]AGCTAATCCCAGGCA | 221178 |
rs142967628 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233350 | TCCTAAATAGTATGC[C/T]TGGGGTAGACATGCA | 221178 |
rs142985889 | snp | C/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977846 | CTGTAAGAACTGTAC[C/T]AATAATTCTCTCCCA | 221178 |
rs142986707 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038587 | TAAAGTGCCGAGAGT[A/G]AGGATTTTAGGCTCT | 221178 |
rs143024769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065346 | TGAGGGGTAGCAGAT[C/G]GGAGGCAGAGCATGT | 221178 |
rs143025590 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246532 | TGCCTGCGTTTGTGC[G/T]TGTCTCTGTGTGTGA | 221178 |
rs143026160 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002772 | AACAGGTTTCCTACC[C/T]GCTGCTGCTCTGCAG | 221178 |
rs143026653 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040556 | CTGTGGACATTGGAA[A/G]GCAAGGGTAAATAGA | 221178 |
rs143027773 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152600 | CACAGCTCCCACATC[C/T]CCGTCTGTGTGACCA | 221178 |
rs143033936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088453 | ACATGAGAACCCAAG[A/C]CCATCACCCTGGACA | 221178 |
rs143041984 | in-del | -/ACTAAGGAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064988 | GAAACTGTCACAGGC[-/ACTAAGGAG]CACAGGAGCCAGGAT | 221178 |
rs143065054 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054157 | AAGGACACCATGAGA[A/G]ATCCCTCGTCTGCCA | 221178 |
rs143075723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219933 | CTGGTTTCAACCCTG[A/G]AAGTCCCATATCCTG | 221178 |
rs143080676 | in-del | -/CAGACTCTTGCTCTATCTCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24238158 | TTTTTTTTTTTGAGA[-/CAGACTCTTGCTCTATCTCC]CAGACTCTTGCTCTA | 221178 |
rs143091119 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209096 | ACTGATGCAGGGGTC[A/G]TTCTAACGGAGGTGC | 221178 |
rs143095901 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281575 | TCATGGACGTAAGCA[A/C/G]CTGGTTCTCCTGGAA | 221178 |
rs143099878 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145214 | AATGTGTAAATCCTA[C/T]TGCCCTGAAAGAATC | 221178 |
rs143133356 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146781 | CTATGCTTCCTGCAG[C/T]CTCAAATGCCCTCTA | 221178 |
rs143139976 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077964 | GATCTCAGCCTTGAT[C/T]TGAGGACCTTCAAGG | 221178 |
rs143142817 | snp | A/G/T | 0.00252631 | 0.035451 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223245 | ACATGGAACACCCTC[A/G/T]CCTCCTTCCGGAAAA | 221178 |
rs143144511 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213316 | CTGAAACCCAGGCTG[C/G]AGTGCAGTGGCATAA | 221178 |
rs143146326 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304143 | CCAAACAGGGCATAA[A/C]CATGTCACGTGAGCA | 221178 |
rs143150137 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284600 | AGCTGGGAGGCGGAG[G/T]TTGCAGTGAGCTGAG | 221178 |
rs143163814 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039682 | GGGTCCATAGGTTGT[A/G]AGTTTCTTTTTCTGC | 221178 |
rs143171741 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049818 | TCTGCAGGGCCCTTT[A/T]CAAACCAGGAAGAGG | 221178 |
rs143174799 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199349 | TGTAAACAGCTTTGA[C/T]TGTTAGGGAATCTGT | 221178 |
rs143191525 | snp | A/C | 0.00119737 | 0.0244387 | missense, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24017697 | GTAGCTGGTGCAGAA[A/C]CTCGGTAAGAAGGGC | 221178 |
rs143198207 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185694 | TTCTCAATTCCTGGA[C/T]TTAACTTAGAACACA | 221178 |
rs143203514 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042365 | CAAGTTGGAAAGCCA[A/C]TGATGCAGTTCTAGC | 221178 |
rs143206614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120130 | AGGCACTTAGGCAGT[C/T]CTCAGCCCTGTCTCC | 221178 |
rs143243319 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026126 | TACTTTGTTGGTTAC[A/G]TTGGTTGCAAATATA | 221178 |
rs143265778 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190217 | ATTATATAACATATC[A/G]TATATAATATATATT | 221178 |
rs143266823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283478 | CTGCTCAGTGACAGA[C/T]TGTTGGCTTTGCCAA | 221178 |
rs143273235 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139927 | CAAAACATTAGCTGG[A/G]CGTGGTGGCGGGCAC | 221178 |
rs143275717 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084387 | CTCCCTTAAGATGGG[A/C]AGGATGCCCGGGGAA | 221178 |
rs143282324 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202158 | ATTCGTTGATACATC[C/T]AAGTTTATCCTTGCC | 221178 |
rs143287545 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231638 | GTGGAATTGCTAGGT[C/G]TTGTGACATTTCTAT | 221178 |
rs143295987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040286 | CTGGACAAAGGCCCC[A/G]TGTGTCTCACAAACC | 221178 |
rs143305047 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103978 | GTGACTCTAAGTAGG[A/G]CCGATTCCAGCACTT | 221178 |
rs143311576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225539 | GCATTACAGCAAGCA[A/G]GGGGGCTTGTTTCTG | 221178 |
rs143312914 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127559 | GATCTCCAGCACAGC[A/G]AGAGCTCAAGAAATG | 221178 |
rs143320307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193153 | CCTTCAGGAAGCTTT[G/T]TCTGGCATGTGGGCG | 221178 |
rs143334169 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028299 | AAGTCTTTTAGAGAG[G/T]ATATCTTGTTGGTAT | 221178 |
rs143335066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287451 | TAGAGGCGTGAGCCA[A/G]TGTGCCCGGCCCCTC | 221178 |
rs143338279 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088771 | GTTCTGAGAGCCAAT[A/C]TGCCATCATTTAATC | 221178 |
rs143340907 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007230 | GAGTTTAATACCCTT[A/C]TGCTGAGTGACATGT | 221178 |
rs143378628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025576 | GTTCCAATTTATATG[G/T]AAAACAGTGGCATAT | 221178 |
rs143410347 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099219 | CCTGCTTTATCTCTA[C/T]AGGTGATACCAACTG | 221178 |
rs143421484 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283520 | TTTCCCAAGAAAGAA[A/G]ATCTGACTAGCAGGG | 221178 |
rs143423533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222648 | CAGGGATGTATATTT[G/T]CATCTTTCCTTCAAC | 221178 |
rs143432894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034133 | CGACATTTAGCAGCT[A/G]TTTAAAAGACTGTTT | 221178 |
rs143449576 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191579 | CAGTGGCGTGATCTT[A/G]GCTCACTGCAAGCTC | 221178 |
rs143458270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184959 | CAGAGTCCTAGCAGC[C/T]GTATGGGTCATTCCT | 221178 |
rs143459429 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274140 | TACACATTGGCTAAC[G/T]CAGAGGTTTCCAGCC | 221178 |
rs143469217 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027706 | TGTGACCTTGGTCAG[A/G]TAACTTAACTTCTCT | 221178 |
rs143482052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083927 | CAGGGCAGGAATCCA[A/G]TGAAGCATCTCATGA | 221178 |
rs143484909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200324 | CCTGTTGTATGTTTC[A/T]TAGAGCAGTATTTTC | 221178 |
rs143497097 | snp | C/T | 0.000247229 | 0.0111155 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24294799 | GGCCTGTCTGATCAA[C/T]GAGCGCAAGCGCAAG | 221178 |
rs143498385 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090178 | GTCAGATTTCCCCCC[A/G]GTTCTCTGCACTTGG | 221178 |
rs143509413 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265889 | TGCAGAAACAACAGG[A/G]AAGCTGCAGCAGGTG | 221178 |
rs143524330 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280250 | TGTCTCTGTCCAGAG[A/G]TTTTTCTCCTGGTAC | 221178 |
rs143551990 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204951 | ACATCAAAATAATAA[C/G]AGCCATGTATGACAA | 221178 |
rs143552297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180509 | TTAATTATAGGATCA[A/G]CTTGCAAATCATGCA | 221178 |
rs143559243 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245120 | TTTCTTTGGTGCATC[C/T]GTGGGCCCCGGCAGC | 221178 |
rs143569532 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993038 | ATTATGTGCCTGGGC[A/T]CGGTCCAGGCTGCTG | 221178 |
rs143575849 | snp | C/T | 0.0818113 | 0.184966 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269801 | GCTATGTTGCCCAGG[C/T]TTGTCTCAAACTCCT | 221178 |
rs143588824 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080203 | AAAAGGATTCTTCTC[C/T]TTCACATGACCGTAT | 221178 |
rs143602356 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235324 | GTCAATGCAAACTTT[G/T]AGATTCGCTGTCCAG | 221178 |
rs143603821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104881 | TCCTCGCCAGAGGCC[A/G]TGCCAAACCCTTTCA | 221178 |
rs143620528 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168601 | GATGGTAAAGACCAA[A/C]CTCCATTGTGTGGTC | 221178 |
rs143625338 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029312 | TGCTTTTACCAGATG[C/T]GTCAGGACAGTACAA | 221178 |
rs143668207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071123 | GAGGAACTAGGGATG[C/T]GTAGAAAACTAGTGC | 221178 |
rs143686275 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171720 | GAACTTGCAGATTAA[C/T]GGCATACCCAAACCT | 221178 |
rs143694716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107817 | AATAAGATGTGTACT[A/G]CTCTATCGGCACGTT | 221178 |
rs143701283 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170790 | GTGTACTTTCAGATC[C/T]ACTGAAAGACCTGGA | 221178 |
rs143708263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259386 | TTTCTTACTCTGGTA[A/G]ATGTTTTCTGCACAG | 221178 |
rs143711168 | snp | C/T | 9.89821e-05 | 0.00703429 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24289070 | CACTATTTTTGGAAA[C/T]ATTGAAGATATTTAC | 221178 |
rs143727519 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072225 | CAATGTAGAATCAAT[A/G]CTGAAAATTAATTTT | 221178 |
rs143733404 | snp | A/C | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159695 | ATTATAATGTCATAC[A/C]GAGTTTTTTCAATAT | 221178 |
rs143737974 | in-del | -/C | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999287 | AGTGCTATAGGTCCT[-/C]CATTTTTTTCCAAGT | 221178 |
rs143766689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123092 | AGTAAATTCTTCACT[A/T]TATTCACAGATCATT | 221178 |
rs143807383 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170309 | TTCTAAAGCATAGTG[A/G]CTTATTCAGTTTCAG | 221178 |
rs143829548 | snp | A/G | 1.64773e-05 | 0.00287026 | missense | SPATA13 | GRCh38.p7 | 13:24302748 | TCTGGCACACCTTCA[A/G]CAGGCTCACCCCCTT | 221178 |
rs143832809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130525 | AGTGTTCTGATTTAT[C/T]GACTACCTTTCAACT | 221178 |
rs143882136 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013355 | CACCCACTGGGCTGA[C/T]GATCCTCTCCCACTT | 221178 |
rs143882816 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240043 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 221178 |
rs143889062 | snp | A/C | 1.65847e-05 | 0.0028796 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286782 | GCGAGTGAATCAGGA[A/C]GAGCTGTCGGAAAAC | 221178 |
rs143891173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243249 | TGTTACTACGTTACG[A/G]CTCTTTTAAATCATC | 221178 |
rs143905714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250409 | AATATTTATCCGGGT[A/G]TCCAGTGAGCACTTT | 221178 |
rs143916712 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074825 | AACTCCATGCTGCCA[C/T]GTGGTCAGAGAGGAT | 221178 |
rs143931435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990563 | GCTCTATTCCTTCTT[C/T]CTCTAGCAAGTCTTG | 221178 |
rs143934550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139554 | GTGCTGCAGAAAGCC[A/G]TGTCCTCCAAATTTT | 221178 |
rs143937104 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252955 | TGGGTATCCAGTGAG[C/T]GCTTTGAAAATACAA | 221178 |
rs143943599 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140514 | CAAACACAAGGGTCA[C/T]GTGCAGAAGCAGAGC | 221178 |
rs143949158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204972 | TGTATGACAAACCCA[C/T]AGCCAATATCATACC | 221178 |
rs143952386 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296463 | CTTTTTGATTTTGGA[C/T]GCTGACATTTAGGGG | 221178 |
rs143963425 | snp | A/C | 0.000284464 | 0.0119227 | missense | SPATA13 | GRCh38.p7 | 13:24249754 | GCTGCCCCAAAGGAG[A/C]CCGGAGAAGGCGCCC | 221178 |
rs143980016 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104968 | TTTCTCTGCCTGACA[C/G]TCTCATGTCCATCCT | 221178 |
rs143982170 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042089 | AACTCTAGGGGCAGC[A/G]CAAGCTCCCTTCAGG | 221178 |
rs143985398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011355 | TCTCACGTTCCGCAG[C/T]TGGTCTGGGCCCAAG | 221178 |
rs143989113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153758 | GGAGGTCATTTTGAA[A/G]TATCCATGGAGATTG | 221178 |
rs143991348 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195327 | TTCAATTATGTGGAT[A/T]TCAAATTTTGTTTAT | 221178 |
rs144000401 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219395 | ACCCCAATTTTTTGC[A/G]TGTGTTTTATGAAAT | 221178 |
rs144001476 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257934 | AGCTGGCCAGTGAGT[A/G]GTGAAGAGAGGAGTG | 221178 |
rs144005076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015474 | CCTGCTTCCAAGCTT[A/G]TTTCTCCTGTGGCAT | 221178 |
rs144023929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010047 | AGATATGAGACATCA[A/G]TCAAATACATGTAAG | 221178 |
rs144025911 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202707 | AGAACTGTCTTATTA[A/G]ATAGTTTTTTTCTTT | 221178 |
rs144035261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055506 | CAGAGGTCTTAGAAC[A/T]GTGCCCGAAGCACCT | 221178 |
rs144049733 | in-del | -/T | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233623 | CATTTTCTAAGTCAG[-/T]TTTAAAAAAAAAAGT | 221178 |
rs144049762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156310 | ACCGTTTATTCTCCT[C/G]TTTTGCCTGTAGCTG | 221178 |
rs144053716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116250 | TCTTCTCACTGTGTC[C/T]TCACGTGATGGACAG | 221178 |
rs144061933 | snp | C/T | 0.0134286 | 0.0808331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222777 | GCAGAGGGGCTACTG[C/T]GTGGGAAATGGCTAA | 221178 |
rs144066375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255101 | ACCAGGAGTGCGCAC[A/G]AGCTAAATCCTTGCC | 221178 |
rs144096772 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059045 | GGCGGAATCTCCACT[C/T]ACTACAAGCTCTGCC | 221178 |
rs144099077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221295 | CTCAGTGACGTTATG[C/T]TTTCCAAGACCTTAG | 221178 |
rs144101110 | snp | A/C/G | 0.0123082 | 0.0775209 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154945 | TCAGTGCAAACTCCA[A/C/G]CTCCCAGGTTCAAGT | 221178 |
rs144133880 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157693 | CTGAAATGAGGAGAA[A/C]GGAGTTTCCTTTCTG | 221178 |
rs144133938 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118252 | ACTCACTCCCCATCA[A/T]GGTCTCTTTTTACCA | 221178 |
rs144138727 | in-del | -/A | 0.381891 | 0.212379 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201409 | TGGGTCAATATTGAT[-/A]TTACTATTAACTAAA | 221178 |
rs144140946 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224873 | CAGGTACTAGATTCT[C/G]GGGGAAAAAAATAAG | 221178 |
rs144157914 | in-del | -/A/AT/ATT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998927 | TTTTCACTAACTTTG[-/A/AT/ATT]GTTTTTTTTTTTTTT | 221178 |
rs144159055 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24060361 | TTCAATAAATGGTAC[C/T]GGGATAACTAGCTAA | 221178 |
rs144166466 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121684 | GAGTTTTATACTGCA[A/G]ATGAGACATTTTAAA | 221178 |
rs144187270 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24165274 | TGCCTGCCTCAGACT[A/G]TCTCCCACCCCAGCA | 221178 |
rs144189234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057159 | ATATGTATACATGTG[C/T]CATGCTGGTGCGCTG | 221178 |
rs144193870 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101165 | ATGGCCCTGGCCCCT[G/T]TTGCTCCTCTACTGT | 221178 |
rs144198333 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992893 | GCTTCTAACAGTGCC[A/T]GGCACGGCAAGAGCT | 221178 |
rs144205733 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233104 | CTCCATTTATTCAGC[C/T]GCCTATGGTTTTTGT | 221178 |
rs144213074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285999 | GCGCTTTCTTTAAAA[A/G]CAGGTAGAGATGTCC | 221178 |
rs144214302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297100 | CTGGAGTGTACTGGC[A/G]TGATCACCATTCACT | 221178 |
rs144217709 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996934 | CCCTCTCAGATCATC[A/C/T]TGGAGGCAGGGGCTG | 221178 |
rs144226447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036317 | CTGTCCTTATCTGTT[C/G]TTACATTTAGGCTGA | 221178 |
rs144242080 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187452 | AAAACAGCGACCGGC[A/T]TACGTTTTATTCTGC | 221178 |
rs144253712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059895 | ATGTTGAATAGGAGT[A/G]GTAAGAGGGGCATCC | 221178 |
rs144271447 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195558 | TGCCCCATTTTACAG[C/T]CCACCAGCAATATAA | 221178 |
rs144279514 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129777 | TGGCATCAGCTTACC[A/G]TGTGGCCAAAGCCTG | 221178 |
rs144290947 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301982 | AAATCATATCATTTC[C/T]CCAGTAATCCCAGCT | 221178 |
rs144307920 | in-del | -/AC | 0.154329 | 0.23097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188395 | TATTAAGAAAGTGAA[-/AC]AGCCTTATCGCTGAT | 221178 |
rs144313608 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033976 | ATTTATGGAAGAGGA[A/G]ACCCTTTATCTGCAT | 221178 |
rs144324423 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281255 | TCCCCCTCCAACCCC[A/G]TCTCTTGGTCTCTTA | 221178 |
rs144328737 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032280 | CCCATGCTGTATTCA[A/G]CACTGAGCCTGCTCT | 221178 |
rs144336209 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198133 | CCCGAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA | 221178 |
rs144337583 | in-del | -/A | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256281 | ATAAGTCCTACTGTG[-/A]CCACAGTTAATGACA | 221178 |
rs144339441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240549 | ATGGAGTTTGTCACC[A/G]TCATGCGGAGTTCAT | 221178 |
rs144340231 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134433 | CACAGAGGCAGATGG[A/G]TGGGGGTGCGCCTGC | 221178 |
rs144342703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093228 | GCCTGGTTTCAAGCA[C/T]GTTTTATAAAGGGTG | 221178 |
rs144344140 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095728 | ATCTACCCTCGTTTC[C/G]CTACAAATTTGGTTC | 221178 |
rs144347146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182867 | TCAGTCGGGCCAGGT[A/G]AACAAAGCTAGTCCA | 221178 |
rs144356154 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246596 | CGGGTGTGGTGGCTC[A/G]CGCCTGTAATCCCAG | 221178 |
rs144361587 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306239 | TAAGTATTTTGTAAA[A/T]GCCAGCTGAACCAGC | 221178 |
rs144375315 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994885 | TTAAAAGCATATCAG[C/T]ACACTGTTATGAAGC | 221178 |
rs144379523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145232 | CCCTGAAAGAATCTG[A/G]TTTTTTACAACAGCC | 221178 |
rs144382923 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081265 | GGGACAAAAAGTGAA[A/G]AGTTGAGTTAATCAT | 221178 |
rs144393306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301758 | GACTTACACAGTTAC[A/G]TTTTAATCTAATCGC | 221178 |
rs144398985 | in-del | -/CT | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151199 | TCCCGCAGTGCTGAG[-/CT]CTATCTGTGCTGTGA | 221178 |
rs144399271 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100129 | TGATTTATTTTATAA[A/T]TTTTAAATAGTTTAA | 221178 |
rs144403967 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036886 | GTTCAAGCGATTCTC[C/T]GACCTCAGCCTCCCG | 221178 |
rs144404522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046891 | GTTCACTGAGACAGC[G/T]GTATTGCAGTAGAGA | 221178 |
rs144407080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243470 | AAGTACATGCTAAGT[A/G]TGCAGGCTTTCCAGA | 221178 |
rs144440505 | in-del | -/TGCCCAGAGTAGCCTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987064 | ACATGGGGCAGGCCT[-/TGCCCAGAGTAGCCTG]ACCCCATAGGCAGTG | 221178 |
rs144445550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001543 | GGGTGGCCGGGCTGG[C/G]TGCCGTGTCTGTTAG | 221178 |
rs144451390 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208257 | GATCAGCTTTCTTCC[A/G]GAAATTCCCTGTAAT | 221178 |
rs144473173 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206454 | AAGGAATGCTTTTAC[A/G]CTGTTGGTGGGAGTA | 221178 |
rs144478923 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103616 | TGTTACTTAAACATA[C/T]AGCTTGTATAACTGT | 221178 |
rs144478987 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141414 | GGGCCTTGCTAATGC[A/G]TTTGAATCTTCTGCC | 221178 |
rs144483316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172986 | TAGTTTCATCAGCAT[C/T]GTACGGCTTTCAGCA | 221178 |
rs144501510 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986168 | CATGTACACATTAGG[A/T]ATTTCGGCTCGCCCA | 221178 |
rs144501887 | snp | C/G | 0.000153988 | 0.00877328 | missense | SPATA13 | GRCh38.p7 | 13:24294759 | ACAGCAACATAAAGG[C/G]AGCATATGAGGCCAT | 221178 |
rs144513838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042573 | AGCGCACATCTATGC[C/T]CGTGCGCGAACTCAC | 221178 |
rs144520440 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073178 | GGTGTTGGAAGGCCA[A/G]GTGGGGGACTGTAGT | 221178 |
rs144525764 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162080 | GTGCCTGTCATGCAC[C/T]CTCCCTGTTCTCTGC | 221178 |
rs144531473 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230462 | GGTCTTTAGTGCCCC[A/G]GGCGGCGGTTGCAGA | 221178 |
rs144536098 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005216 | GTTCTGTTTTCTGGT[A/G]GCCTGGCTATTGTGC | 221178 |
rs144545087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105989 | GAACTGTGAGAAATA[C/T]GTTTCTGTCGTTTAA | 221178 |
rs144554022 | in-del | -/AAAT | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120205 | CCGCCTCTGAAAAAA[-/AAAT]CAGGATTCTACTACT | 221178 |
rs144562791 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179354 | GGAAGAATTGCCAGA[C/G]TATTTCTCAAGCAGG | 221178 |
rs144584982 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278237 | CAGTTCTGCCCAGTG[G/T]GTAAGAGTTAGATGG | 221178 |
rs144609318 | in-del | -/T/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24280492 | TTTACTGAGATGCAC[-/T/TT]TTTTTTTTTTTTTTG | 221178 |
rs144612930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218242 | AGGTGGAAGGTAATG[C/G]AGGCTGGGAATGAGG | 221178 |
rs144619841 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216838 | GGAGGACGATTTGAG[A/G]TCAGGAGTTTGAGAC | 221178 |
rs144622866 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280344 | CCAGCTTTTTTTCTT[G/T]CTTTACTGATTTTCA | 221178 |
rs144639411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116011 | TCTCAGAAGTCACAC[A/G]CCATCATTTCTGCAA | 221178 |
rs144641468 | in-del | -/TCTGATTCACTGTGGCC | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254181 | ATGGCCAGCCTTGGT[-/TCTGATTCACTGTGGCC]TCTGATTCACTGTGG | 221178 |
rs144647032 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133979 | GGGGGCTGGGTCGAG[C/T]CCCTGGGGGAAGGCT | 221178 |
rs144651483 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222286 | AGTTAGTGTTTGGGC[A/G]TCTCAGCCCTCCTGG | 221178 |
rs144664315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254646 | GTAGGGACAAATCAC[C/T]ACCCCCTCTATTATG | 221178 |
rs144669194 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005053 | GTTATCTTTGCCACA[C/T]TGCTTTCCATTTTAA | 221178 |
rs144684055 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067390 | TCAAATAGGGATTTA[A/G]TCATTAAACTTAAGA | 221178 |
rs144687306 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154532 | CATTGCTAACGGGGG[A/G]GAGGGGCACATAAGG | 221178 |
rs144689619 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178574 | TGCATTGCTAGGAAG[C/G]TATTATTATCTGTAT | 221178 |
rs144700602 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080382 | CGACTTACTAGAAAT[C/G]AGAACAAAAGCTTTG | 221178 |
rs144716677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184136 | TGTGGCATCTGTTGA[C/T]GACTGTGTCTGAATA | 221178 |
rs144723701 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020807 | CCAGCACTTTGGAAG[A/G]CTGAGGTGGGTGGAT | 221178 |
rs144753088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023837 | TTGGTTTTAACCTGC[A/G]AGACCCCTGTTGAAC | 221178 |
rs144758463 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116659 | TCACAAATGCAAAGT[C/T]ACTGAGGTAGGATTT | 221178 |
rs144760113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079279 | ATCCAGGGCCTTGTC[C/T]GCTACGGTGCAGTTT | 221178 |
rs144767235 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083331 | ACCAAACCCTGCCCC[A/G]CCCACAGGAGTCCAT | 221178 |
rs144781503 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085088 | CGATGTTGATCTGGA[-/G]TGTGTAGTGTGGCAT | 221178 |
rs144792612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062363 | GGGCAGGAGGCCAGG[G/T]ACTGACTGGGGGCTG | 221178 |
rs144804621 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215621 | TAAAATGCAACACAC[A/T]TATATGCTCTTACAC | 221178 |
rs144813077 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028421 | CTGGGTTGGTTGTTA[A/G]TTTCTCCTAGTACTT | 221178 |
rs144821555 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081499 | GAGGCTGTAGGTCTC[A/G]TTCTATTTCTTACTA | 221178 |
rs144831030 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086254 | TGTAAGTGTATCATT[C/T]ATATTGCATGGTACA | 221178 |
rs144831398 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114268 | GGGGGTCTGTCCAAT[C/T]AGATTGTGAATCTTT | 221178 |
rs144846419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267005 | GGTTTTCGTTGTAGG[A/T]TTCTTACTGATCTGG | 221178 |
rs144854483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983439 | CAGTCCCATTCTGAG[A/G]TACTGGAGTCAGGAC | 221178 |
rs144877512 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198194 | GAGACGGGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 221178 |
rs144877954 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189479 | CTCCATCTCTCTCTC[-/CT]TCTCTATATATATAC | 221178 |
rs144884978 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989314 | GTAGTCCCAGCTACT[C/G]AGGAGGCTGAGGAAG | 221178 |
rs144886470 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288753 | GTATTTGAAACTTGT[G/T]TCTGGAAACATTATA | 221178 |
rs144902961 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099001 | CAGCTTCTCAGGAGG[A/G]TTGAGCTGAGGAGTT | 221178 |
rs144904059 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037423 | TTATTTATTTATCTA[C/T]TTGAGATAGAGTCTC | 221178 |
rs144904596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261926 | AGTTCAAAATACCCC[A/T]TAAAGGCTCAGGACT | 221178 |
rs144925506 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002675 | GACTGCCGCAAGCCT[C/G]GTCCGGCTCCTTGAG | 221178 |
rs144939850 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259936 | TGAGCCACCACACCC[A/G/T]GCCTGAGTTGGATTT | 221178 |
rs144968291 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231065 | ACTTGGCTCCCCCCA[G/T]AAGGCTTCCCCACGC | 221178 |
rs144982780 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258454 | GGCAGATCACTTGAG[A/C]CCACAAGTTTGAGAC | 221178 |
rs144992097 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282875 | ATGCCCACAGAAGGG[C/T]AGGACCAGAATTCAG | 221178 |
rs145007806 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157739 | GAAACCCCTGCTGAA[C/T]GGAACTTTCAGCAGA | 221178 |
rs145013243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095524 | TGAAAGTGGGAATGC[A/G]CCTGATGCCACGGAG | 221178 |
rs145017381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184005 | AAAACTGAAACACAC[A/G]GGAAGTGGCGCGCTC | 221178 |
rs145018692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264334 | CAAGACAGCTAAATG[C/T]CTAGCGAACCACCAC | 221178 |
rs145031463 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198184 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 221178 |
rs145036488 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100500 | TCTCTCAGCTATTTC[C/T]AGTAGCACATGTGGC | 221178 |
rs145044879 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998286 | CTAAAGGTATGTAGT[A/G]GTATCTTGGAGTAGT | 221178 |
rs145045338 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165061 | TCAGGATGTCAGCTT[C/T]GGTGGACACAGGTAA | 221178 |
rs145049972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260917 | ATGCCTTAAGTTATG[C/T]TCATGGCATGCGTGC | 221178 |
rs145070341 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082876 | CTTTGCATTATTCCC[A/G]CTTACATACAATAAG | 221178 |
rs145073597 | in-del | -/C | 0.340784 | 0.232934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028961 | CTAATAATTTTACTT[-/C]CTAAAGTCCTGGTGA | 221178 |
rs145080255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167597 | GAATAGTGTGAATGG[A/G]AATGTTATGTGAATT | 221178 |
rs145083605 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146513 | ATAACTAAGTACTCT[A/C]TAATCTTATCTACAT | 221178 |
rs145088895 | in-del | -/A | 0.230017 | 0.2492 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196902 | TATTGGATTGGCTAG[-/A]AAAAAAAAACAGTTT | 221178 |
rs145095160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162998 | AGAAAAACCTAATGC[C/T]GGCTGTCCCTCAGAA | 221178 |
rs145113939 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130973 | GGGTGGAGCGGGGGA[C/T]GCTTTCTGGCTTCAT | 221178 |
rs145134062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002566 | CAGGGGGGTGAGTGT[A/G]TTGGTCTTTGAGTCT | 221178 |
rs145134345 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | SPATA13 | GRCh38.p7 | 13:24290700 | AACAACCACCCGGGC[A/G]CCTGCCTGGAGCTCG | 221178 |
rs145147562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034464 | AATGTACCTAACAGG[C/T]CTTAATAGAGAAAGT | 221178 |
rs145162337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165915 | CCTAAACAACTTGCA[C/T]ATGTACTTTTAAACA | 221178 |
rs145192781 | snp | C/G | 0.000153988 | 0.00877328 | missense | SPATA13 | GRCh38.p7 | 13:24297565 | AGCTTGTGGACCTGG[C/G]GGATGGGCGCGACAA | 221178 |
rs145195183 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246275 | TTATTCTCACTATGT[A/G]CTTAAGTTGTCTGTG | 221178 |
rs145196203 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286855 | CAGAGCCGCCACAGA[C/T]ACTGTGAGAACAAGC | 221178 |
rs145209996 | snp | G/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067969 | TTGGCCTCCCAAAGT[G/T]CTAGGATTATAGTTG | 221178 |
rs145220617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276853 | AGAGGTGAAGAAGGC[A/G]GCAGCACCGGCCTGT | 221178 |
rs145224762 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005416 | AATATAGTGCTCACC[G/T]GGTGCCTAGCAGGGT | 221178 |
rs145238759 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085035 | TGTGTGTTCGCAGTC[A/G]CCTGGGATTCTGGGT | 221178 |
rs145243551 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174638 | CTGGAGTATAGTGGC[A/G]CAATCTTGGCTCACT | 221178 |
rs145250073 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264210 | CAGTTCTCAACAGCT[A/G]GAGTTAAAAAGTAAA | 221178 |
rs145260920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009542 | TGGTCTGGAAAGATG[A/G]GACAACTTGAAGCAG | 221178 |
rs145262793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248962 | GCAACTTTTGCCTCC[C/T]AGGATCAAGCAATTC | 221178 |
rs145281600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075982 | CTAGCAAATCATGCG[A/G]TGGAAACACCTTCTG | 221178 |
rs145309991 | snp | A/G | 1.65037e-05 | 0.00287256 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24251765 | GGTGCCACCCTACAA[A/G]GCTGTGTCGGCCCGG | 221178 |
rs145310044 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026754 | AGCTAATTTTTTGTA[-/T]TTTTAGTGGAGACGG | 221178 |
rs145317336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212692 | TTAAGTTTAAACACA[C/G]TTAAGTGGGTCACAC | 221178 |
rs145325972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213876 | CTACTTGTTCAACAG[C/T]TTACAGAACATTTTA | 221178 |
rs145326704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282037 | TTTTCCATGTTTATC[A/G]TTGTTCTAGTGCCAG | 221178 |
rs145333967 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147919 | ATCCATGTTGTAGCA[C/T]GTGTCTGAATCTCCT | 221178 |
rs145365678 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040132 | AAATCCCCCAAACAC[A/G]GACAGGCTTGAGATG | 221178 |
rs145390855 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218022 | ACAAAACTCGCAAAG[A/C/G]CATGGTGGTGTGAGG | 221178 |
rs145396850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113131 | CTTGAAAGGCTAACC[A/G]GACAATGTCCACTTT | 221178 |
rs145397215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152338 | CTGACTCTAGCACAA[A/G]GCACAGCCCCAAACA | 221178 |
rs145402091 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082268 | AAGCACGTAAGTGTT[C/T]TGTGGCAGGGGCAGG | 221178 |
rs145416438 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24244265 | TGACCTCATTTTAAC[-/T]TTTATTATATCTGCA | 221178 |
rs145420370 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145722 | CAGGTGGAGAGAATT[A/G]TGCATGATCAATAAA | 221178 |
rs145429428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983017 | AGGAGCTGGAGAGGG[A/G]CTCCCTGGAGCAAAA | 221178 |
rs145430738 | in-del | -/T | 0.455621 | 0.142197 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157289 | CTTTTTCTTTTTTTT[-/T]CTTTTTAATATATTT | 221178 |
rs145437784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167151 | GTCATAGGTGAGGAT[A/T]CCATGAATTGATCCT | 221178 |
rs145440245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103147 | TCTCATGAACTTCAC[C/T]TTAAAAATAGTTCTG | 221178 |
rs145445224 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053565 | ACCCTTATAGACTTC[C/T]CTTGCCACCTGGGCC | 221178 |
rs145450882 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977715 | TCTGGGTCTTCTGGG[G/T]TTTTGTGAGTCTGTT | 221178 |
rs145451876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256004 | CACAGATAGTGAAAT[A/G]CTTTCTGCATAAAAT | 221178 |
rs145457859 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048300 | GCATTTTTAGCATTA[C/T]GTTATATTGTTTAGA | 221178 |
rs145463066 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987347 | TACTTACATTTTCAG[-/T]TGGATAAAAGATAGC | 221178 |
rs145464120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115678 | ACATTCATCATCCCA[C/T]ACAGTGTCAGAGGGT | 221178 |
rs145469516 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006273 | TCATAAGATGTCACT[C/T]TTGAGTGTTCATGAG | 221178 |
rs145473710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068951 | TATTTTCTCCCATTC[C/T]GTAGGTTGTTTGTTC | 221178 |
rs145483886 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24222353 | TGCTCCTCATGCTTA[C/T]TCCTGCGTGTGCCAG | 221178 |
rs145485239 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149732 | AACCCAGAGGGAGAG[C/T]GGCTTGTACAAAGGC | 221178 |
rs145496024 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077216 | ATGGAACAAATTTTC[C/T]TACGAGAAATAGCCC | 221178 |
rs145513071 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057462 | GAAGCCAGTGTTGAC[A/G]GGGCATTTTCTGAGT | 221178 |
rs145527388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021659 | TATACGCCGTGCATT[C/G]GGCATTATTCACCAG | 221178 |
rs145550929 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051611 | TAGTAGAGTGGAGCC[A/T]GCGGAGACAATGCTC | 221178 |
rs145552075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300071 | CTCCTTCTGGGGCCT[C/T]ATCCTTTAGGTTATA | 221178 |
rs145566249 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063916 | GACTTCCTTAATGAC[C/T]TGAGGTCTTCGTTCC | 221178 |
rs145568859 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023073 | TAGGTATTTCTCCCA[A/G]TGCTATCCCTCCCCT | 221178 |
rs145575597 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125013 | TGGCAGACAGGAAAC[A/G/T]TTAGAGAATGTCAGG | 221178 |
rs145584312 | snp | A/G | 0.0009981 | 0.0223171 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24249815 | TGGGACCAACCAGAC[A/G]GAGGAACTGGACAAT | 221178 |
rs145585463 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279149 | GGAGAAAACTAAACC[A/C]GGGGAGACAGTGGAG | 221178 |
rs145590418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020120 | ACCAGCTGCATACAG[C/T]TTCTCCCTGTTGGCA | 221178 |
rs145612401 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232067 | GAACCAATAGGATAC[A/C]TATGAAAATCGGCTG | 221178 |
rs145621864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115237 | CAGGTGCCTCTCACA[A/G]CAGCAGTCATGGCAG | 221178 |
rs145623614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294957 | TTAATATCCTGTGGT[C/T]AATATCTTATATTCT | 221178 |
rs145645775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234771 | CAGCTGCTTGCTGCC[C/T]TGCACTGATCTAGTA | 221178 |
rs145656991 | snp | C/T | 0.000576525 | 0.0169685 | missense | SPATA13 | GRCh38.p7 | 13:24297451 | AAAGCCAGCAGCGGA[C/T]GTTCTTCCTGTTTGA | 221178 |
rs145658480 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299545 | AGAGCCTGAGCCTGA[C/G/T]GTCAGGACAGTCTGG | 221178 |
rs145672750 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131743 | GGATAGGGACAACCA[A/T]TGTGGACCCTGGCTG | 221178 |
rs145678276 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197539 | TATAGGGCAGTAAAA[C/T]TGTAACCTTTATAGT | 221178 |
rs145678284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237096 | GGGCGCAGGGCTCAC[A/G]TCTGTAATCCCAGCA | 221178 |
rs145704356 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196283 | GAGGCTTGGCATAAA[C/T]CCTTCACACATTACC | 221178 |
rs145716754 | snp | A/G | 0.00204467 | 0.0319089 | missense | SPATA13 | GRCh38.p7 | 13:24289041 | ACAGGAATGTTCACC[A/G]TTGCGCAGCTAGCCA | 221178 |
rs145724860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244008 | CCATTCTGGAGGCCA[G/T]AAGTTTGAGATCAAA | 221178 |
rs145731690 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198615 | TTACATCAGTTTCTA[C/G]ATAAATGTTGATTGG | 221178 |
rs145742449 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057114 | ACTTTAAGTTTTAGG[A/G]TACATGTGCACAATG | 221178 |
rs145756742 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247365 | ACTGATTAACTGTGT[-/G]GCCCTGGGCAAGTCA | 221178 |
rs145758741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142743 | TTTCTCCTTCTCCTT[A/C]TCCTGGCGTTTTATA | 221178 |
rs145773006 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298729 | CTAAAAACCAGGAGG[C/T]GCTTTTTCTGTCCTC | 221178 |
rs145774764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037861 | GTATATATATCATTC[C/T]TCAGAAATTTTACTC | 221178 |
rs145778181 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 13:24043525 | CTCTGTGCACATGCA[A/T]CTTGCACACCCAGAG | 221178 |
rs145779940 | snp | C/T | 0.00874735 | 0.0655527 | | | GRCh38.p7 | 13:24125808 | AGGACACAGGAAGCC[C/T]AGTGCTGTTGTTGAC | 221178 |
rs145786559 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 13:24022328 | AGGCGTGAGCCACTG[C/T]GCCTGGCGAAAAATC | 221178 |
rs145791550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106999 | ATTTGCTCTCTGAAA[A/G]CTATATTTCTGGGAA | 221178 |
rs145806731 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259289 | AGGGAGGGGGCAGAG[C/G]AAGGGGCTTCCACCC | 221178 |
rs145808479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099879 | ACTAAACTGTCATGT[C/T]TGTGAATGAACACTT | 221178 |
rs145823321 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012801 | TGCCCAGAACACCAC[A/C]CTGAGCCCCGTGGCT | 221178 |
rs145839360 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031077 | ATCTTCTCCCATTCA[A/G]AGTAGCAAATGGTTT | 221178 |
rs145859529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200829 | AACAAATAAAACAAA[C/G]CAAAAAACCCCACTC | 221178 |
rs145865125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003413 | TAATGAATGGAGTGC[A/G]CACAGGAAAGGGTAC | 221178 |
rs145866902 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040105 | AAACTTCCACTAAAG[A/G]CCATTCAGCAGAAAT | 221178 |
rs145875484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993481 | TTCTCTGCAAATAAG[A/G]GAAAGCATGCACCTC | 221178 |
rs145898808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006525 | GGGAGGCTCAGGGCA[C/T]GAGGTGCGGCAGAGG | 221178 |
rs145927078 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214775 | TGCTTCTGCCTTGTA[A/C/G]AGGGTAACATAACCT | 221178 |
rs145940828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074342 | CTAGGATTTCCTTCC[C/T]TTTTTAAGGCTGAAT | 221178 |
rs145943355 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998966 | AGTCTTGCTGTGTCA[C/G]CCAGGCTGGAGTGAA | 221178 |
rs145946101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177223 | AGTTACTTTTAACAA[C/T]TAAGAAATTTTTAAT | 221178 |
rs145954598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018587 | AGAGGTCTACGCATT[A/G]ATAGCCAATGATGAC | 221178 |
rs145958996 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077888 | TGGGGCCCACAACTC[G/T]TTGTTCCCTTGGTTG | 221178 |
rs145981300 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021946 | TCGATCTCCTGACCT[C/T]GTAATCTGCCTGCCT | 221178 |
rs145988137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237341 | GCACTCCAATGCTGG[C/T]GGCAGAGTCAGATTC | 221178 |
rs145991400 | in-del | -/AAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135716 | AAAAAAAAAAAAAAA[-/AAA]AAGAGTATTTTTAGA | 221178 |
rs145992917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982067 | AAAACATGTAAAGAT[A/G]TGTGTGTTTTAAAGT | 221178 |
rs146006721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172612 | GTTTGTTGAAAAAAC[A/G]TCCTTCTTGCATTCA | 221178 |
rs146008574 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225187 | GATCCCATGCCTGCC[A/G]AGGGCAAACCAGGAA | 221178 |
rs146027292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229697 | TTAGTTTGACATCAT[A/G]CTACTTAAAAAAAAA | 221178 |
rs146033796 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291264 | GAAAGCCATAACTCT[G/T]GTTCTCTCCTGTACC | 221178 |
rs146042136 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124244 | TATTAAAATGTGTTT[C/T]TGTTGTCTTTAGTAG | 221178 |
rs146043683 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239949 | TGGTCATTATGTGCA[-/T]TTTATTTCATAATAT | 221178 |
rs146048930 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198028 | TGAGATGGAGTCTAG[C/T]TCTGTCGCCCAGGCT | 221178 |
rs146061514 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060090 | CTATTTCAAAATTCA[C/T]GTGGAATCAAAATGA | 221178 |
rs146065727 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160237 | CTGGTGGCTGAGGGA[A/G]CTATTTTTGTTTGTT | 221178 |
rs146082133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062746 | TGTGTGTATGTGCAC[C/T]GTGTCTGCATGTGTC | 221178 |
rs146084217 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000740 | GGAGAGCTCTGGGTC[A/G]GAGGCATGAATTTGG | 221178 |
rs146100313 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24066423 | CATACGGCCCGGAGG[G/T]GAGACTCCCAGAGCT | 221178 |
rs146111126 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241839 | GGAGGACTGCCTGAG[C/T]CCAGGAGTTTGAGAC | 221178 |
rs146116337 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175367 | GCTAAAAGTCTACAT[A/T]GCCAATTTAGGGCAA | 221178 |
rs146152503 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209690 | CACTTAGGTCAATTG[C/T]GTATCTTGGCTACTG | 221178 |
rs146155353 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274512 | TCATGTTTTGACGTT[A/G]TCAGTTCCTGTGACC | 221178 |
rs146165849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110882 | GACTGAAATATGTTT[A/G]CACCATCTCTGCGCA | 221178 |
rs146199853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046078 | CTGTGCAGAACCATG[C/T]GTTAGATTTTTTTTT | 221178 |
rs146219107 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076889 | CCTCTTGGATTCACG[G/T]CCAGATGGGCTGACA | 221178 |
rs146226596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014527 | TGTAGTCTTACAATA[A/G]AGTAAGCTAGAGAAA | 221178 |
rs146237171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018084 | GAATCACCTTACACC[C/T]GTGGAAAACCAATCA | 221178 |
rs146251438 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254934 | TGATTGATTAGCCTC[C/T]CTTGCAATAAGGATT | 221178 |
rs146270169 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257739 | GTGATACAGTAATAC[A/G]AATTGCTAGCAGGCA | 221178 |
rs146270770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194480 | CAGCTCTGTGAAATA[C/G]GAGAAACCAACTAGC | 221178 |
rs146285533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094565 | TCTTTCTTTATGCTT[A/G]AAATGTTTTTAAAAA | 221178 |
rs146301793 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089549 | CCCCTCTGGGCTAGG[A/G]CAATCAGTTAGTGTT | 221178 |
rs146306247 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193779 | TGTGGAAACGTAGCT[A/G]TTCCTCAGTGAGCAA | 221178 |
rs146318107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032918 | CTGGGAATACTGGGG[C/T]GTTTGATAAAGTCCT | 221178 |
rs146321768 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093525 | TTCAGGCACGTTTCT[C/G]ATACACCCCAAAAAC | 221178 |
rs146324765 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013413 | CCAGCTCTGGGGCCC[A/C]TGGGCAGCCCCCTCA | 221178 |
rs146344840 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034799 | GAGTCCTAGGAGTGA[C/T]TGTCCCCAGAGAGCA | 221178 |
rs146345080 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996283 | GTTTTAACACTAGAG[C/T]TTGCAAATGAGAAGA | 221178 |
rs146348823 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111983 | TATATTCTCTAGATC[A/G]TTTTGAATTGGATAA | 221178 |
rs146352027 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275876 | GAGGCAAAGGCTGCA[C/G]TGAGCTGAGATCGCG | 221178 |
rs146358384 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000346 | AAAGGGAGCAGCAGG[C/T]GACAAAGTCCAGTGA | 221178 |
rs146368027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174930 | GATTATTTAGAAATG[C/T]GTTGTTTCATATCCA | 221178 |
rs146372033 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240251 | ATGACAGAGTGAGAA[A/C]CTGTCTTTAAAAAAA | 221178 |
rs146373450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278445 | GCAATTCTATTTTTA[A/G]TTTTTTTTTAATTTA | 221178 |
rs146391510 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243446 | CAAAGTTCTGTTTTC[C/T]TTCTGTAAAAGTACA | 221178 |
rs146393293 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177619 | TGCATGCCACCATGC[C/T]TAGCTAATTTTTTAA | 221178 |
rs146407115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078263 | AAACTTTGGAGCCAG[A/G]CACGCCTCTGTTTGA | 221178 |
rs146427586 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015547 | ACCCTGTTGTGAGCT[A/G]AGTCAGGCCTGACCC | 221178 |
rs146456606 | snp | A/G | 0.000787329 | 0.0198254 | missense | SPATA13 | GRCh38.p7 | 13:24251862 | ATGAGAGCATCCAAC[A/G]GTGAGTCTCAGAGTC | 221178 |
rs146457197 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255390 | TTGCCAGCCCTGGAG[A/C]GTTCCTCCTACACAA | 221178 |
rs146466383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076154 | TGCATTCTTGACTGA[G/T]AAGTTCTTAGAAATT | 221178 |
rs146472004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154999 | TGTAGCTGGGATTAC[A/G]GGTGTGTGCCACCAT | 221178 |
rs146487141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017270 | TCTCTTATCCTCATC[C/T]GAGAAATAGAATAAT | 221178 |
rs146490233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118394 | TAGTTACTCCTGGCA[C/T]GTGTGGATTATTTAT | 221178 |
rs146510364 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121877 | CCCCCTCGATCCCCC[A/C]AAATCCCGCTGGTTT | 221178 |
rs146525003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027119 | CTTTTTGTTCCTGAT[A/G]TTTTTTGTTTAGCCG | 221178 |
rs146580925 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198721 | TTCTGCCAAGTCTGG[A/G]TCGTCCTGTGAGGGC | 221178 |
rs146583311 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306253 | AAGCCAGCTGAACCA[A/G]CATTTTATCAGGTGG | 221178 |
rs146599028 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201633 | TTTAGTAGAGACAGG[A/G]TTTCACCATGTTGGC | 221178 |
rs146602299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268365 | AGTCTTTTGAGCCTA[C/T]AATTTAATAAACTAC | 221178 |
rs146616625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167426 | GTAAGCTAATCCCAG[A/G]CAAAGATACAGAAGA | 221178 |
rs146629560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105999 | AAATACGTTTCTGTC[A/G]TTTAAGCTACCCAAT | 221178 |
rs146629751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069622 | TTTATTTATCTTGCC[C/T]GATTGCCCTGGCCAG | 221178 |
rs146629831 | in-del | -/CAGCC | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006756 | GAGCACCGGGACACG[-/CAGCC]CAAGCTCCTGGTGCC | 221178 |
rs146634470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169992 | TATTTTAAATGTGAC[A/G]TCTTCATACAAAGTT | 221178 |
rs146647827 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071876 | AAGATGATTCTCCCC[A/G]TGTGCACTTTAAAAC | 221178 |
rs146649694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012528 | GGCAATTTTGATAGG[C/T]TTCTCACTTGGCCCT | 221178 |
rs146670886 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042395 | CCTTTGTGGAAAGAT[A/C]CATAGGCCGCTTTCT | 221178 |
rs146677919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283480 | GCTCAGTGACAGATT[A/G]TTGGCTTTGCCAAGG | 221178 |
rs146684376 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980904 | CCAACAAAGTTTTTT[-/T]AAAAAATACGTTGTA | 221178 |
rs146696212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287554 | AGAAGGCAACACCCT[C/T]ACTTGATTTTACAAA | 221178 |
rs146696742 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248028 | TTGTCCTCCCTGGGC[C/G]CATGGCCTGACTGAC | 221178 |
rs146698150 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184162 | GAATAAGTTTTGAGT[C/G]AATGGGTACCTGGTG | 221178 |
rs146729691 | in-del | -/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050193 | CTTTCTGAACCATCT[-/G]GGGGAAGTCACAGTA | 221178 |
rs146731615 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086430 | GGTCGAAGAAGACAC[C/G]AGGGAGAGGGCTGCT | 221178 |
rs146737149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151239 | TGCGTCCTTCAGCAT[C/T]CAGGTTACATCAGGA | 221178 |
rs146749779 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978525 | GTACTTTTGCATTTA[A/T]ATAGCATCTTTTGTA | 221178 |
rs146750600 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090470 | TGAGCTCCTCCTGAC[C/T]GTCCCCTCACCGAAC | 221178 |
rs146791439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988609 | AGATTGTACCAATTC[A/G]TGTGTCCTTTATAAA | 221178 |
rs146791570 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029805 | GATAGGCCCCAGTGT[A/G]TGTTGTTCCCCTCTA | 221178 |
rs146798432 | snp | A/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268777 | ATGAAATAAAATTTC[A/T]GTAAGAGAAAGATTT | 221178 |
rs146799791 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259277 | GCTGCTGTCTGCAGG[A/G]AGGGGGCAGAGCAAG | 221178 |
rs146799878 | snp | C/T | 0.00340309 | 0.0411092 | utr-variant-5-prime, synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24222869 | GTGTGAGTGCCAGGA[C/T]GGCATTCCTGGAGAT | 221178 |
rs146802838 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992438 | CGCCTGGATACAGAC[A/C]ATTGCAGGTGTGTCT | 221178 |
rs146816609 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234005 | AACTTTCCAGTGGCT[C/T]ATTTCTAGAATAGTT | 221178 |
rs146816664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271014 | CTCTCTCTCTCCACT[C/T]TCTCTCACTCTCTCT | 221178 |
rs146818139 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156659 | TAAAATATAGCAAAC[A/G]CACCTTATCCATTCT | 221178 |
rs146833010 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170559 | AAGTCTCCTGTGGAA[A/G]CGCCATCCCCTCTGC | 221178 |
rs146835878 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236466 | TGGGCGTGGTGGCAC[A/G]CACCTGTAGTCCCAG | 221178 |
rs146852890 | snp | C/T | 0.00665121 | 0.0572832 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24302680 | TATGCCCACAAGCGT[C/T]CCCCAGCAGCAGGTC | 221178 |
rs146854047 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072191 | TGGCTTGTAACTAAC[C/T]CTAGACATACAGAAC | 221178 |
rs146858227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174014 | CCTCTTTCATTTCCC[A/G]GAAGAGGTAGTGTAG | 221178 |
rs146861719 | in-del | -/ATACAGACCAG | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133182 | TAGACTGTGCAGCCT[-/ATACAGACCAG]ATGATAGCACAGAGA | 221178 |
rs146875412 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037598 | TATTTTTAGTAGAGA[G/T]GGAGTTTCACCATGT | 221178 |
rs146877824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139736 | TACATGATGTAGAAC[A/G]ATCTGCTTAATTGAT | 221178 |
rs146887126 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039760 | TTGGGGGAATTCTGT[A/C]GTTGGCTTTGTGCAT | 221178 |
rs146897132 | in-del | -/GAT | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265427 | TCACTCTCGGCACTC[-/GAT]GATTTAGGGGAATGG | 221178 |
rs146899011 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226983 | AGAGGTCTTGACTAT[C/T]GAGAACCGTCTGCTC | 221178 |
rs146913019 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061640 | ACCAAATACTATATG[A/T]TCTTACTTATAAATA | 221178 |
rs146924630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993687 | AGTGAGAATTTACCT[A/G]GGAAAGCCCATCCTT | 221178 |
rs146928210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096789 | AAGAGAGCTCAGTGG[A/G]CCCAGCCTGGGTAGG | 221178 |
rs146928551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058632 | GCTTCAAAACGGTCT[A/G]CATAATTATGAAATT | 221178 |
rs146932013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158277 | ACAGAATGCAGATGC[C/T]GGCCTTGTCTGCGAG | 221178 |
rs146944673 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061014 | ACTGCACTCCAGCTG[C/G]GGCAACAAAGCAAGA | 221178 |
rs146947466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999735 | AATGTTTGAAAACTG[A/G]TGTTTCTTATATTTA | 221178 |
rs146987529 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204260 | TACTGTTATCCACAT[C/T]TTTCATTTTGCAGAT | 221178 |
rs147009375 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273050 | GTCAGCCAGGATGGA[C/T]GGGAGGAGCCGTGCT | 221178 |
rs147016759 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108527 | CCTACTGAAGGAAAC[C/T]GCTTTAGGGAGGGCT | 221178 |
rs147031584 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040711 | TGGATCCAAATTGTA[C/T]CAATTGAAAGGGGGA | 221178 |
rs147034003 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079595 | GCTAGTAATACAGGG[G/T]GGTCCTGACGGCTTG | 221178 |
rs147037943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143019 | AGCTGACCCTGAGAC[A/G]ATGGCTTGAGTCCAA | 221178 |
rs147045491 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23979983 | TGGAGAAGGTAGAGC[A/C]AAGCAGCATTTGGCC | 221178 |
rs147054564 | snp | C/G/T | 0.00478244 | 0.0486902 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044088 | TGAGAAGCTAAAGCC[C/G/T]GGAAGGTGGAGGGCT | 221178 |
rs147068407 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983689 | TGAATTCTATATCTA[A/G]CTTGCTTCATAATTT | 221178 |
rs147080320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290002 | GGCCCCATGTGTGAC[A/G]TGGGCATATCTGGGA | 221178 |
rs147097022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294177 | TTTAGCTTGACGTGA[C/G]TGTGGTGGACGGAAA | 221178 |
rs147110064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192834 | AGGCCTTCTGCATGG[C/G]TGGAACTGCCTAAAA | 221178 |
rs147112666 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256112 | ATAATCGTGGGTTCA[C/T]GGTATTATCTGCTTT | 221178 |
rs147121294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092927 | AATGTTTTGGTGTTT[C/G]GCATCTTCTCATTAA | 221178 |
rs147125926 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156169 | ATATCTGTTCGAGTC[C/T]CTGCTTTCAGTTCTT | 221178 |
rs147138303 | in-del | -/TTTTTTTTCTTTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262300 | TTGTTTAAAACAAAG[-/TTTTTTTTCTTTTTTT]TTTTTTTTCTTTTTT | 221178 |
rs147148207 | in-del | -/TG | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979296 | GTGAGTGTGTGTGTG[-/TG]TGTGTGTGTGTCCTT | 221178 |
rs147164773 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232874 | ATATTTTTTAAAGAG[C/T]CAAAATTCTTAGTTT | 221178 |
rs147164796 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270009 | TTACAGGCATGAGCC[A/G]GCGGGCCCAGCTTAA | 221178 |
rs147182574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169074 | GCTCGGCTTACTAAA[C/G]AGCCTGCTTGTGTTG | 221178 |
rs147194440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071191 | GATTCCTTTGTAGAG[G/T]AGACAGCTGCATCTC | 221178 |
rs147198946 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134339 | CCCCCTTCCCAGTGA[C/G]TAGTTATCCTCTGGA | 221178 |
rs147201038 | snp | A/G | 0.000148345 | 0.00861106 | missense | SPATA13 | GRCh38.p7 | 13:24294810 | TCAACGAGCGCAAGC[A/G]CAAGCTGGAGAGCAT | 221178 |
rs147207327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036708 | ATCTCTTCTGTGAAG[A/G]CTGCTCTCACCTTAC | 221178 |
rs147210740 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24072965 | AAACTCTATATGTGG[G/T]GTTCCTTTAGCATTT | 221178 |
rs147215304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137648 | CCTCTAATCCCAGCT[A/G]CTTGTGCGGCTGAGA | 221178 |
rs147261573 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260114 | GATGAATGGGAAAAA[-/C]CCACCACAACTGCAC | 221178 |
rs147269613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216508 | CATATACTTTCAATT[C/G]ACAAACATTGAACTT | 221178 |
rs147285765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219620 | TTTGAAGGCAGCCAT[A/G]TAAAGCTATCATTAT | 221178 |
rs147288489 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153939 | AAACAAGTGTTATCT[C/T]ATGAGGACATTTATG | 221178 |
rs147301395 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056128 | GGGATGAAGGGCACC[C/G]CTCAGAATTTCACAG | 221178 |
rs147305408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116255 | TCACTGTGTCCTCAC[A/G]TGATGGACAGAGCAA | 221178 |
rs147313738 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022111 | GCTGGAGTGCAATCT[C/T]ATCTCACTGCAGCTT | 221178 |
rs147317998 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059116 | AGCTGGGACTACAGT[C/T]GCCCACCACCATGTC | 221178 |
rs147322270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119321 | GGAAAAAAAAGGGTA[C/T]TTGAGCCATGTTCCC | 221178 |
rs147361642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235882 | AAGTAACTGTTTCTT[A/G]AAAATAAGAATATAA | 221178 |
rs147372249 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134460 | CTGCTACATAGAGGT[A/C]GTATGGATGCCGAGA | 221178 |
rs147380930 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304936 | AACAAAATACAATGA[C/T]ATATGTTGGAAACTA | 221178 |
rs147388514 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137945 | GACTGGTTGTTATTG[A/T]GTGTTCTTGAAATTT | 221178 |
rs147392289 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200121 | ACAAACCCCTTCAAC[A/G]GGCATTTTCTTAATT | 221178 |
rs147405679 | snp | C/G | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102498 | TTTTTTTTTTGAGAT[C/G]GAGTCTCACTCTATC | 221178 |
rs147408658 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039291 | CTACCAGCTACTACT[C/G]AATTTACCAACCTGG | 221178 |
rs147418688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005229 | GTAGCCTGGCTATTG[A/T]GCTCACATTTGAAAA | 221178 |
rs147421375 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104370 | AAAGCAATTTAGCCC[A/T]CTCAATTTTTAGAGA | 221178 |
rs147423017 | in-del | -/C | 0.0854556 | 0.188216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143942 | TATCTCATGTGGTTG[-/C]CCTGAAACCACAGGG | 221178 |
rs147467016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220279 | GCCCTTGTTTCCTTC[C/T]TGGTTATAAAAGGTC | 221178 |
rs147469006 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281813 | GAGAGAGGGGCTGGG[A/C/G]CCGGGCTGGGAGAGG | 221178 |
rs147470905 | in-del | -/C | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088614 | ACATCTCTTTAACCT[-/C]CAATTTTCTCTTTCC | 221178 |
rs147481962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183278 | CAAATATAATAAACA[C/T]ACATTTTCTTGAGGA | 221178 |
rs147485355 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284899 | CCACATTTTCATCAA[C/T]GCTCTAAGGAAAGAT | 221178 |
rs147498403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186515 | ACGAATAAAAATAGG[A/G]CATCAACAATGTTCT | 221178 |
rs147501768 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250107 | TTTGTTTCTGAATAA[C/T]CTGAGATTCTAACCA | 221178 |
rs147515401 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149542 | TCTAGTGTTCATTAG[A/G]GGAGTTCTGCTGCCA | 221178 |
rs147524380 | in-del | -/T | 0.0569829 | 0.158885 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276716 | TTTTGGTGACATACA[-/T]TTTGAGAATTTATAA | 221178 |
rs147527759 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088960 | TGGAGACAGGGATGC[A/G]GTCATCGACAGCTCT | 221178 |
rs147532136 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153197 | TAGCTGCCTGGCAAA[A/G]GAGCTGTCATGCTGG | 221178 |
rs147543640 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054808 | TATTCATTTTTTAAA[C/G]TGGAAAAATGAATTC | 221178 |
rs147546269 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991034 | AGAAGATGAAGCCCG[C/T]TCAAGGTTAAGATCA | 221178 |
rs147553826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261258 | CGAGGTAATTGTCTG[A/G]ATGTTTGGGGCCAGG | 221178 |
rs147555048 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24158381 | ACACAGAGGCCACAT[A/T]GTGATTCCCGCAGGA | 221178 |
rs147570510 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230974 | ATAACATCAACTCAC[C/T]GGTTGTAGGTATGCA | 221178 |
rs147571805 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163025 | AGAAAGCCTGGGGCC[A/C]GTGCCTGGGCTGTCA | 221178 |
rs147584175 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064545 | CCCAGAGAACTCCCA[C/T]GCCCTTATTGCCATG | 221178 |
rs147588043 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125339 | ATTCCTAATGAGACT[A/C]ACCTTATTGTCTTGG | 221178 |
rs147600287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068294 | AGTTTGCTAAGGATA[A/G]TGACCTCCCTACAGA | 221178 |
rs147605031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128630 | CATTCTAACACTCCT[C/T]GCTGATGTGGACAGG | 221178 |
rs147613311 | snp | C/T | 1.65529e-05 | 0.00287683 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286911 | GGAGATCATGGACAC[C/T]GAGCGGGTGTACATC | 221178 |
rs147619855 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033704 | AGCGAAGTAGGGGGA[G/T]ATTGCGTAGTGTGCT | 221178 |
rs147629761 | snp | A/C/G | 4.95252e-05 | 0.004976 | missense | SPATA13 | GRCh38.p7 | 13:24251779 | AGGCTGTGTCGGCCC[A/C/G]GTTCCGGCCCTTCAC | 221178 |
rs147643010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212742 | GTCACTTTGCCAGAT[A/G]TTGAAAAAAAGAAAG | 221178 |
rs147654610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143023 | GACCCTGAGACAATG[A/G]CTTGAGTCCAAGTTG | 221178 |
rs147658287 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207069 | CATGTCCTTTGCAGT[G/T]ATATGGATGGAGTTG | 221178 |
rs147658537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247284 | TTTGAGCAGAGGTGA[C/T]GTGGCATTGCAGGAA | 221178 |
rs147671474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145737 | GTGCATGATCAATAA[A/G]TAGAGAACGGCTAAT | 221178 |
rs147674482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210794 | TTGTATTTCATTGGA[A/G]TTTCAATAGCCATGG | 221178 |
rs147690985 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048503 | TACATTCATAATTTC[A/G]TGTAATAATACATAT | 221178 |
rs147703581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114524 | CTTGGCATCTCAGGC[A/T]GTCAACTGGCTGCCA | 221178 |
rs147713873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294340 | CTGTTGAAAATGGTT[A/G]GTGATTTTTAAAGTA | 221178 |
rs147723800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020203 | GATCTGTGTGTTTTA[A/G]TGTTTTGGTATTTTA | 221178 |
rs147729655 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298262 | TTGGCTGTGCCTGTG[C/T]AATACCTTCAGTGTT | 221178 |
rs147745718 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258483 | ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCCATC | 221178 |
rs147747660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196692 | AGTGAGCTGTGATTA[C/T]TGCACCACTGCATTG | 221178 |
rs147759789 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126449 | TTTCTCCTTCATGTC[A/C]CTTAAAACCCACGAC | 221178 |
rs147764063 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233202 | ACAGAATTTGAATCA[C/T]AAAAATTAGAGTTAG | 221178 |
rs147767213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297307 | GCTTCTTAAGTAGCT[A/G]GGACTACAGCTGTGG | 221178 |
rs147776163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129949 | GCCTGTACTGCTCCC[A/G]GGTGGAGAAATTCAC | 221178 |
rs147780775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195722 | CCAAGTTACTGATTT[A/G]TTGATTTCACTGTAA | 221178 |
rs147794628 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034000 | TCTGCATCGCAATTC[C/T]GAAGATTCCACTTTG | 221178 |
rs147804782 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999124 | TAGAGATGGGGTTTT[G/T]CCATGTTGGCCAGGC | 221178 |
rs147827608 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001639 | CACCAGGGCACCACA[C/G]TCATCCCAGTGACTT | 221178 |
rs147850792 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244780 | ACACGGGAGGATCAC[C/T]TGAGCCCAGGAGGTG | 221178 |
rs147864790 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112107 | GGCCCACAGGACACT[C/G]TCTAGGCTGTCCTTC | 221178 |
rs147869862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175067 | AGGTTTGTATGGCCC[A/G]GGGTATTGGTCCATC | 221178 |
rs147869906 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216869 | CAACCTGGCCAACAT[A/G]GTGAAACCCTGTCTC | 221178 |
rs147892857 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020870 | GAGATGGTGAAAACC[A/G]GTCTCTACTAAAAAT | 221178 |
rs147898070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079546 | GAAGTTTCAGCTGAT[A/G]ATCCCGACCTGAGAC | 221178 |
rs147914780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081968 | ATGAGCCATAGGTCA[C/T]ATGCATATCTATTTA | 221178 |
rs147916735 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979403 | TACCCCAATTCTTTT[C/G]CGCTGATCCTCAAGC | 221178 |
rs147926613 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983505 | TTTTAAAAAGTGGAC[A/T]CTGATCTGTGACTTT | 221178 |
rs147945527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289455 | TTTTTAAAAATTTCT[A/G]AGGGTTATGCCATAA | 221178 |
rs147959674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231075 | CCCCAGAAGGCTTCC[C/T]CACGCCTTTTACCAA | 221178 |
rs147969067 | in-del | -/CG | 0.438105 | 0.164671 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189494 | CTCTCTATATATATA[-/CG]TGTATATATATATAT | 221178 |
rs147972632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184985 | TTCCTCAGGAAAGTG[C/T]GGGTGCCTTTGAAAG | 221178 |
rs147980085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274199 | TTGTGGCTTGCTGCA[C/T]GGACAGGCAACAAAA | 221178 |
rs147990963 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083979 | TTTAGGTGTGCCGTT[C/T]GCAAGAGTCACCACA | 221178 |
rs147996537 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238249 | GCAGTCTTCGCCTCC[C/T]GGGTTCAAGCGATTC | 221178 |
rs148005373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986174 | CACATTAGGTATTTC[A/G]GCTCGCCCAGGGACC | 221178 |
rs148018683 | in-del | -/AAAG | 0.474 | 0.111014 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098619 | AAAAGAAGAAGAAGA[-/AAAG]AAAGAAAGAAAGAAA | 221178 |
rs148023450 | in-del | -/TA | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017122 | GGCAGAGAGTTGAGG[-/TA]ACATCAGTAGATGAG | 221178 |
rs148026526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181254 | ACTTAGTCCACTCTA[A/C]ATGTATTTAATATAT | 221178 |
rs148030590 | in-del | -/AC | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045362 | TTAGCCTTATTTTAT[-/AC]ACACACCTTTTAGTA | 221178 |
rs148042746 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143842 | ACTTACTTGGAGGAA[A/C]ATGTGACACTTTCTC | 221178 |
rs148045537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235493 | TGGCTGACGTGGTGG[C/T]TCATGCCTATAATCC | 221178 |
rs148047517 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300261 | TCTGATCTTCAACCT[G/T]TCCACGTTCTTTGAG | 221178 |
rs148059662 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044715 | ATTTTGAAATATACA[A/G]TACATTATTGTTAAC | 221178 |
rs148061832 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198034 | GGAGTCTAGTTCTGT[C/T]GCCCAGGCTGGAGTG | 221178 |
rs148062955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134197 | ATGAATTTCTCTCCC[C/T]AGCATGAGGACTTCG | 221178 |
rs148102655 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24289097 | TTACAAATTCCAAAG[A/G]AAGTTTCTGAAAGAC | 221178 |
rs148107265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072289 | CTCTCTTTAAGTACC[A/G]TACAGCAGAAGAGAA | 221178 |
rs148111216 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136256 | GTGAGGTGGGTGGAT[A/C]ACCTGAGGTCGGGAG | 221178 |
rs148114821 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228450 | CAAAAAGAGAAAATA[C/T]AGTTATGGCTTTACC | 221178 |
rs148116757 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160152 | GAACTTCTGGCCCAG[A/G]CAGTGGGCAGTGGGG | 221178 |
rs148123221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037905 | AGTAAAAGGTTAGTA[A/G]CAACTAGACTAGATT | 221178 |
rs148133192 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123282 | ATTTCTCTATCATCA[A/G]TCAGACATCTTCTTG | 221178 |
rs148167019 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222756 | AGCGTGCCTCTTCTT[C/T]TGTGAGCAGAGGGGC | 221178 |
rs148171970 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24199015 | TGCAGTGGTTCATTC[-/T]CTTTGTTCTCTTTTC | 221178 |
rs148175913 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034234 | AGTCAGCAATCTAAA[C/T]TTCAAACCTCAGGGA | 221178 |
rs148183603 | in-del | -/G | 0.0391387 | 0.134304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141842 | GGGTAATAATGTGCT[-/G]TCTCAGAGCAGGCTA | 221178 |
rs148185496 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152927 | CTTTTACATTTTACA[C/T]TGAGACTTTCACCTC | 221178 |
rs148187384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243295 | CTCTCATTTTCTTTT[A/T]TGCATGTGAACATAT | 221178 |
rs148189471 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218462 | AGCCTCACTGGGCCC[C/T]AGCATCCTCACTGGC | 221178 |
rs148198089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054340 | GAATGTGAAGTTTAA[C/T]GAAATTAGCTCTGTC | 221178 |
rs148202732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116092 | TAGATGTCCTAGACC[A/G]TTCAGGCTGCTATGA | 221178 |
rs148235705 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163719 | GTGGTCCAGGGAAAT[-/A]AAATGGCATATTCAA | 221178 |
rs148241727 | in-del | -/AG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185818 | CATACATCAAGAGAC[-/AG]AGAGAGAGAGAGAGA | 221178 |
rs148245449 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304407 | GAGATGCTGTGTTAA[A/G]CTGTTAATGGATATC | 221178 |
rs148253359 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175789 | AAACTAGAGAGACAC[A/G]GATCTAGGTGTCATT | 221178 |
rs148256475 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112379 | GTAGTGCTCCCCACA[C/T]TGTATGACAATCAAT | 221178 |
rs148259209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199735 | TGGAATTTTCAATAG[A/G]CGCATAACAGTGTCA | 221178 |
rs148262192 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264995 | TGAGAGCACATATTC[A/G]CTGGTTTTGTGTGTT | 221178 |
rs148266042 | in-del | -/GCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24075798 | TCTGCCGCTGGTCTT[-/GCA]GCAGCCTGTGGGTGG | 221178 |
rs148271271 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017721 | GAAGGGCCTCGAGTC[C/G]GTTCTTCCCTCTCCT | 221178 |
rs148272687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076936 | TCGGCTCTTCAACCT[C/T]GCCTTATTCCTAAGA | 221178 |
rs148275250 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165578 | CCCTTCCCGGTTGCA[C/T]CCCCCACCCACCCCA | 221178 |
rs148292690 | snp | A/G | 0.00320599 | 0.0399089 | missense | SPATA13 | GRCh38.p7 | 13:24284263 | GGGGAGCAGCTGGCC[A/G]TCAATGAGGTACTGG | 221178 |
rs148314715 | snp | A/T | 0.000165308 | 0.00908993 | missense | SPATA13 | GRCh38.p7 | 13:24294750 | GCAGTGATTACAGCA[A/T]CATAAAGGCAGCATA | 221178 |
rs148323374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040504 | TGTGTTCTACAGACA[C/T]ACAGATGGGGTTGGA | 221178 |
rs148324549 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104039 | TTTCTCATTGATGGG[A/G]ACATAGGAACGTTGT | 221178 |
rs148325506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193316 | AAGTAGGTGAGGGTG[A/G]GGGAGAGAGATGACA | 221178 |
rs148329524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281484 | TGTCGCGGTGTCCGG[C/T]GCACCTGTCTGGGTG | 221178 |
rs148331108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256828 | TTTCAGTGGCACTTA[C/T]TGGAGCCTTATCGGA | 221178 |
rs148333493 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007280 | AGAGGAAAGGCCAGG[C/G/T]TAGGCCACTGCTTGC | 221178 |
rs148342383 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156935 | TTGTCCCCTGCCACC[G/T]TCACAACCAACAAGA | 221178 |
rs148384376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002869 | AAATCAAACTCATTG[G/T]TCATCCCTGGGTGAT | 221178 |
rs148386544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065696 | TAATACTAGAATCAC[A/C]TGGTATTGTATTTGT | 221178 |
rs148393301 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977824 | TTTCTTATTTTTCTT[C/T]TGATAACTGTAAGAA | 221178 |
rs148414688 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172991 | TCATCAGCATTGTAC[A/G]GCTTTCAGCACACAG | 221178 |
rs148432585 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230518 | GGAAGAGTGTAGAAC[A/G]GGAGGCAGATGCCCA | 221178 |
rs148447815 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039333 | CTACCTTGCAGACTT[A/T]CGTGGCAGGAAGAAA | 221178 |
rs148490748 | snp | C/T | 0.000304886 | 0.012343 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286167 | GCTCCCTCACCATCC[C/T]GCCCACTCGTGCTCT | 221178 |
rs148495795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067511 | ATACAAGTAGATTCA[A/C]GAAAGTTATATAAGT | 221178 |
rs148498273 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005148 | TTCTCTGAGTCGCTA[C/G]GGGAGAAGTTAACAG | 221178 |
rs148499721 | in-del | -/G | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003927 | AGAAGTCCCTTTTCA[-/G]CCACACTCCCCCTCC | 221178 |
rs148502707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220579 | ACAGGCTTCATATCC[A/G]GTCTCATCGCAGAGA | 221178 |
rs148504621 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154555 | ACATAAGGGAGTCTT[C/T]TGAGGCGCTAGAAAT | 221178 |
rs148520336 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117306 | TTAATTTTAGGAATT[A/G]GCCGTCACTGATTGG | 221178 |
rs148545727 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103543 | GAGAGAGAGAGAGAG[-/AA]GAGAGAGAGAGAGAA | 221178 |
rs148558522 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987039 | GTGTGTGTGTGTGTG[-/GT]TTACTACTCCACATG | 221178 |
rs148559364 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24278627 | AGGGTGCTTTCATGT[A/G]TCATCATTCCACTTG | 221178 |
rs148561642 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028598 | GGAGAGATCTGGCAT[C/T]ATATTCTTTATGCTT | 221178 |
rs148566534 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114384 | ATGTGTGCACATGCG[C/T]GTGTGTGTGCATGTG | 221178 |
rs148570955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177921 | GAGTATGGTGGTACA[A/G]TCATGGCTCACTGCT | 221178 |
rs148574294 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267634 | AAAAAATTTTTGTAG[A/G]AAATGAAAACACTGG | 221178 |
rs148590180 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233237 | ATAATTTTTAAATAT[A/G]ATATTATGTGTGCTT | 221178 |
rs148608098 | snp | C/G/T | 1.65356e-05 | 0.00287533 | missense, synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286806 | GGAAAACTCCAGCAG[C/G/T]ACCCCCAGTGAGGAG | 221178 |
rs148621776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205820 | ACAAACCTGACCAAA[A/G]ACAAGCAATGGAGAA | 221178 |
rs148629820 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296518 | TGCTGACAATTTATC[A/G]TCTGGCCTTTTGTTT | 221178 |
rs148641026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105253 | TCAGCCTCCAGAGTA[A/G]CTGGGACTACAGGTG | 221178 |
rs148644232 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195345 | AAATTTTGTTTATCC[A/G]TGCATCGGTTGATGG | 221178 |
rs148646927 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258258 | AAAAAATAAAAAGAA[C/T]TCTGGATTCTGCCTG | 221178 |
rs148649604 | in-del | -/TCTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057006 | TGTGGCTGTTTTCTT[-/TCTC]TCTCTCTCTCTCTCT | 221178 |
rs148655407 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010174 | TTGGATCTATGATCA[A/G]CCTTTCACTGAATTA | 221178 |
rs148688015 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101840 | GGGCAGAATCATATT[A/C]TGTTGTGTGTGTTTA | 221178 |
rs148695461 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254688 | CTGCAATCAGCTTTC[C/T]GCAAGGGGCTGTCTG | 221178 |
rs148708747 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036381 | AGGAAGAATGTCTGG[C/T]CTCACAGAAGTATGG | 221178 |
rs148710018 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097989 | AAGGACCTCCATGAG[G/T]TTCAGACTGCCTTGA | 221178 |
rs148713109 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187574 | TTGTTACAATAGCAT[A/G]TGCGTACATCTTGTC | 221178 |
rs148714940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277078 | AGAAGATATACCGTA[A/G]AAGAATTTTGTTATG | 221178 |
rs148718787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000922 | ATTCCCTGGGTCAGA[C/G]GTGTGAATTTGGGAC | 221178 |
rs148724345 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085180 | TAGGCTGGAGTGCAG[C/T]GGTGCAATCTGGGCT | 221178 |
rs148753964 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997557 | TCCATTTTGCATTGC[-/T]ATAGAGAAATACCTG | 221178 |
rs148771049 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23995151 | ACCCTGACATCCTTA[A/G]GAGCCTGAAGATACA | 221178 |
rs148782441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145464 | GTTCCTCTGATTGTT[C/T]TCAGTTCATGTGAGT | 221178 |
rs148784559 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236209 | CTTAATCTTTCTTAT[C/G]TGTAAAGTAGAATTA | 221178 |
rs148789748 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301776 | TTAATCTAATCGCTA[A/C]TTTTAATAAACCTTC | 221178 |
rs148792416 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047074 | GTTGGGGATGAAATT[A/G]TAGGGGTGTGGAAAA | 221178 |
rs148801027 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198197 | ACGGGGTTTCACTGT[C/G]TTGGCCAGGCTGGTC | 221178 |
rs148815362 | snp | C/T | 0.031825 | 0.122064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069284 | CATTTGTTTGTGTCA[C/T]CTCTGATTTATTTGA | 221178 |
rs148818065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156062 | GTATGTATTTACTAC[A/G]TCTTGTTTATTCATC | 221178 |
rs148818951 | in-del | -/AC | 0.45645 | 0.140991 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030048 | CCCTACCTTCTCCTA[-/AC]ACACACACACACACA | 221178 |
rs148819328 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129951 | CTGTACTGCTCCCGG[A/G]TGGAGAAATTCACCT | 221178 |
rs148820849 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222585 | TCCAGTGAGCTCAGG[A/T]GTTTACCTTCATGTC | 221178 |
rs148834270 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118662 | ATGCTGGTGCAGTAG[C/T]TTCAGGAAGCACACC | 221178 |
rs148836052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034088 | TTCCTCCACCCACAG[A/G]AAAATTCCTCTAAGG | 221178 |
rs148859731 | in-del | -/GA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24008568 | AGGAGAAGGGGAGGG[-/GA]GAGAGAGAGAGAGAG | 221178 |
rs148876120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218015 | AGAGCAGACAAAACT[C/T]GCAAAGGCATGGTGG | 221178 |
rs148878550 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279160 | AACCAGGGGAGACAG[C/T]GGAGTGAGAGTGAGG | 221178 |
rs148887774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115537 | ACTAATGCCTGATGA[C/T]TTGAGGTGGAACAGT | 221178 |
rs148892121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179586 | AAACTGAAACTCTGT[A/G]CAGATTAAATGCAAG | 221178 |
rs148893643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269337 | ATGCATTTTACTAAT[A/T]GGCACTATCACTTGT | 221178 |
rs148897397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992990 | CCCTGAGAGCTGCCT[A/G]TCATATTTTCACCAA | 221178 |
rs148899511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021469 | CTCTACTCCAGTCTG[C/G]GTGACAGAACGAGAC | 221178 |
rs148903864 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080085 | GCTGGAGAAGTGAGA[A/C]AGTGAACTGTGAATT | 221178 |
rs148921365 | snp | A/G | 3.29919e-05 | 0.00406138 | missense | SPATA13 | GRCh38.p7 | 13:24289059 | GCGCAGCTAGCCACT[A/G]TTTTTGGAAACATTG | 221178 |
rs148946244 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299332 | GCTCAGAGATGCAAG[C/T]GCATGACTGAGGCAC | 221178 |
rs148947498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271581 | ATGTGAAAGAAACTT[C/T]GTACTCTCACACTAG | 221178 |
rs148955601 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107392 | GTCTCTACTATGTTG[C/T]CCCAAGGAGCCCGAA | 221178 |
rs148959257 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170591 | GAGTACATCTCTGTT[A/G]TCCTCAGATTGAGGC | 221178 |
rs148963197 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259369 | CCCAGAGCCTCACTT[G/T]CTTTCTTACTCTGGT | 221178 |
rs148963539 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197446 | ATGAGGGAACCAGCA[A/G]GATGTTGCCACTGAC | 221178 |
rs148968420 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012846 | CTGTTTGGTTTATGC[A/G]TCTGCAGGTCGGGGC | 221178 |
rs148972096 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072224 | ACAATGTAGAATCAA[C/T]GCTGAAAATTAATTT | 221178 |
rs149012053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167348 | TGGTCGTGGTCCTCT[A/C]CTTTGGTCTGAGAGT | 221178 |
rs149014314 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256022 | TTCTGCATAAAATAT[A/G]ATATGTGAGATTTGT | 221178 |
rs149031108 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251265 | TGTCGGTGGGGAGGA[A/G]TAAATGAGGCTGAAG | 221178 |
rs149031642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189339 | AGCCAGGCATGGTGG[C/T]GGGTGCCTATAATAG | 221178 |
rs149043401 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002724 | GCACCTGTGACCCCC[C/T]GAGCACAAGCACTGG | 221178 |
rs149044335 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088307 | GTAAGGAATTGGCCC[A/G]CAGTCACATGACTAT | 221178 |
rs149048033 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152593 | CCAGCCCCACAGCTC[C/T]CACATCCCCGTCTGT | 221178 |
rs149076643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095722 | CTTGCAATCTACCCT[C/T]GTTTCCCTACAAATT | 221178 |
rs149082808 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247632 | GGATTACAGGCACCT[C/G]TCACCACACCTGGCT | 221178 |
rs149088720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998618 | TTTTAGGGATCGTGA[C/T]TTTTTGCTGTATTTG | 221178 |
rs149093325 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060669 | GAATGGGAGAAAATA[G/T]GTGCAAACTATGCCT | 221178 |
rs149101561 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146611 | TAAAATGTTCTTTTA[C/T]AGGGCACTAAGGAAA | 221178 |
rs149107212 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303555 | TCCCTCCTGCCTGCA[C/T]GCCTTCAGTAACTCC | 221178 |
rs149118246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112238 | TGTTCTCTCCTCTGG[C/T]ATTGTAGCAAAGCTG | 221178 |
rs149143872 | in-del | -/A | 0.117537 | 0.212022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051743 | TAGGGGGGAAGTGGT[-/A]AGCGATTGGAGTCAG | 221178 |
rs149154484 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174858 | TGCTGGGATTACAGG[C/T]GTGAGCCCCTGCACC | 221178 |
rs149166484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076127 | TCATTAAGGTAATAA[A/G]CACCACTGATGTGCA | 221178 |
rs149171361 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139894 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA | 221178 |
rs149172168 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231632 | CTAGGGGTGGAATTG[C/T]TAGGTCTTGTGACAT | 221178 |
rs149177102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294362 | TTTAAAGTACTTTAT[G/T]TAGCAAGAGTGGTTA | 221178 |
rs149179761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040149 | ACAGGCTTGAGATGC[C/T]GGGTGGCCAAACCAA | 221178 |
rs149225495 | in-del | -/TGTTATGTATTATATAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024688 | TTTGATGACATAAAA[-/TGTTATGTATTATATAT]ATGTTATATATTATA | 221178 |
rs149226569 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288940 | GCCTACAAAAGCTGT[A/G]CTATTCAAATAATTT | 221178 |
rs149233311 | snp | C/T | 0.000777985 | 0.0197075 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24294745 | ATCTTGCAGTGATTA[C/T]AGCAACATAAAGGCA | 221178 |
rs149257356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058204 | GCTTACATAGGATGA[C/T]GTCTTTTGATCGTAA | 221178 |
rs149262747 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274105 | TTGTCCTATTCGTTG[G/T]AATAAGGAACATTCA | 221178 |
rs149264565 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208090 | GGACGAGCCTTGTTC[C/T]TGTCAAAATGGGCTC | 221178 |
rs149275278 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024255 | GTATGCGCTCTAAGA[C/T]TCTTCAGACTATAGG | 221178 |
rs149276277 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110044 | TTAGAATTGCAAATT[A/T]GGCAGCGGGACATGT | 221178 |
rs149279655 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172774 | CATACATCTTGAAAT[C/T]GGATAGACCTGATTT | 221178 |
rs149287682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014353 | CCCCCCTTCCCCCAT[A/G]CAGAAATGGCCCCAC | 221178 |
rs149332077 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235290 | GACTATCAGCAATCA[A/G]CTCGGGAAAATGACT | 221178 |
rs149333262 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168263 | GATCCAGTTTAATTT[C/T]TGTCAGTTTCTAATT | 221178 |
rs149338283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017543 | ACACACATATGTATA[C/T]ATACATTTTTGTTTA | 221178 |
rs149345091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100789 | TGCTGCCTGTAACTT[A/T]CCCCACTGTTGCAAG | 221178 |
rs149351864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253457 | ATGCAGTGCCTCTTC[A/G]GCGTTGATTAACTAG | 221178 |
rs149353284 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191153 | TAATTATTATTTTAT[A/G]TTTGTAGAGACAGCA | 221178 |
rs149357470 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004848 | CACCTGAGACCCCCA[C/T]ATTAAACCACAAACC | 221178 |
rs149399241 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097739 | CCTGGATCATGTAAG[C/G/T]AGAGGGACCCCCCAA | 221178 |
rs149403544 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159555 | ATTCGAGTGGCACAT[A/G]TGTTATGATTGATGG | 221178 |
rs149417005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000168 | CAGAATGTCAGCTGT[A/G]GTGGTCTAGAAAGGA | 221178 |
rs149417546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149523 | GAGACAATCCCTGGT[C/T]GACTCTAGTGTTCAT | 221178 |
rs149421430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215311 | GAAGACAGTTTAAAT[C/T]AGAAGCAGAAGGCAT | 221178 |
rs149434982 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113918 | ATATAGTTATATAAA[C/T]ACCAACAGAAGTATC | 221178 |
rs149458363 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278121 | AGGGCAGGACATACG[A/G]CTGCTCTCCAGAATG | 221178 |
rs149480697 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990377 | ATGCCCTGGCTCACT[C/T]CCTCTGTTTCCTTGC | 221178 |
rs149485294 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053901 | AGGGATTTTCCAAAC[A/T]TTAGTGAACTCACAA | 221178 |
rs149498949 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295920 | AAAGTAGCAGAGCTG[G/T]ATTCAAACCCAAGCA | 221178 |
rs149507759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042060 | CGTGTGTCACATTTC[A/G]AGGCAGGTGGACCAA | 221178 |
rs149526112 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295258 | TCTGGCCAAGATTAA[-/T]TTTTTTTATCTTATA | 221178 |
rs149541211 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137531 | TTGGGAGGCTGAGGC[A/G]GGAGGATCACTTGAG | 221178 |
rs149547403 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290509 | AGCTTGGGTGCCAGC[A/G]GATTTCATGCCCTGT | 221178 |
rs149562117 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132900 | GAATCACTTGAACCT[A/G]GGGGGTGGAGATTGC | 221178 |
rs149565383 | snp | A/G | 0.0001156 | 0.00760176 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224017 | ATGACGACTACTCCC[A/G]CCGCGTCTCCAGGAG | 221178 |
rs149567641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285118 | TTACTGAGATGGCCA[A/G]TGATGTGTATCGTTG | 221178 |
rs149608397 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126970 | ATCAAACAAAAATGG[A/G]TTTAAATCCTTTCAC | 221178 |
rs149615584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281116 | GGCCCTGCCATGCCC[C/T]TGGCAACCGTCCCCT | 221178 |
rs149621471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032099 | CATGCTTGGTGTCTG[A/G]TTATCCTCCACCATC | 221178 |
rs149625165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093003 | CCAAAGGCCGTGATG[A/G]TTAATCTTATTTTCC | 221178 |
rs149633703 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182856 | GTTGCGCCACATCAG[C/T]CGGGCCAGGTAAACA | 221178 |
rs149645528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080981 | CCCTTTTGTCATTCC[A/G]AGGGTTCTGTCATCC | 221178 |
rs149653923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293955 | TGCTGTAAGTTGCCA[C/T]GGGAAAGCGGAAAAT | 221178 |
rs149665274 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103004 | GCATGTGGCTATCCC[A/G]TTTTCCCAGCACCTT | 221178 |
rs149669778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167057 | CTCTTACCTTCAAAT[A/G]TTATGATTGGTTTGG | 221178 |
rs149670434 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255915 | CTGAATATTTGGCAA[A/C/T]ATGAAGGAATTATTT | 221178 |
rs149675867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006000 | CCATGCTTCGGGATA[A/G]GAGACATCCCCTGAG | 221178 |
rs149681085 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068584 | GGTTGAACTAATTTA[C/T]GCTTTCACTGACAGT | 221178 |
rs149699293 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077151 | AGCAAATAGCTGTTT[C/T]TACCATGCAGGCCAT | 221178 |
rs149716683 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162002 | CTTTCCCAACAAATT[C/G]TCCTTTTTTCCTAAT | 221178 |
rs149719545 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230388 | CAGGAGCCCCAAAGG[C/T]GGCAGAATGAAGAAC | 221178 |
rs149725662 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250687 | ATGCCTTGTCTATAA[C/T]AAGCACTCAAAAACT | 221178 |
rs149732827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124960 | GGATCAAGTGCTTGA[A/G]AGGAACTGAAACTCA | 221178 |
rs149734599 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063634 | TTACACAGCTTCCCT[C/G]AGCCCACTCAAGTGG | 221178 |
rs149741771 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217497 | TGCTGAGAACACAGT[A/G]AAATAAGACAAGGCT | 221178 |
rs149746405 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029871 | ATAAGTGAGAACATG[C/T]GGTATTTGGTTATCT | 221178 |
rs149786152 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003173 | TCTATAAATGCAGGG[-/GT]GTGTGTGTGTGTGTA | 221178 |
rs149787506 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089348 | ATTCTCACAACAGCT[C/T]GGTTGTGGCAAAAAC | 221178 |
rs149791031 | snp | A/C/G | 0.0162516 | 0.088765 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154529 | GGGCATTGCTAACGG[A/C/G]GGGGAGGGGCACATA | 221178 |
rs149794439 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243850 | TATTGTATTTATATA[A/C]ATCTTCAAAAAACTT | 221178 |
rs149803832 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056239 | AAGGAATAGAACAAA[C/G]TGTCCAGAACAGCCT | 221178 |
rs149804146 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992172 | TTGGTAGAAAGTGGA[A/G]AACTGCAGTCCAACC | 221178 |
rs149806510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142684 | TCCTTCTTCCTCTTC[C/T]TCTTCCTCTTCCTTC | 221178 |
rs149812969 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298726 | GGACTAAAAACCAGG[A/G]GGTGCTTTTTCTGTC | 221178 |
rs149818509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043178 | CGCACCGCCTCTCTG[A/G]CTTGGTGGTTTATCA | 221178 |
rs149822884 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106884 | AGCAGATCGAGTGAG[A/T]TTCAGCAAATATGGG | 221178 |
rs149846464 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305465 | GAAAATCTGCATGTC[C/T]GGCTTGGGTTTTATT | 221178 |
rs149863394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266846 | ACCCAGGCTGGTGTG[C/T]AGTGGTACAATCTCA | 221178 |
rs149867876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982959 | CTGGGAAGAAGGTGA[A/G]AGAAACTCTTTCAAA | 221178 |
rs149874971 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135150 | GAAAATAAATTTCTA[C/T]TGTATAAGCCACCTA | 221178 |
rs149883158 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287988 | TCTCTAATCGGATTA[C/G]CCAGCTGTGTGGACA | 221178 |
rs149883376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225881 | GGGAAAGTGTTACAG[C/T]TCCTTTCGCTCCCAC | 221178 |
rs149928708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128601 | CCACAGCCACGCCGG[A/G]CCCCAGAAATCTGCA | 221178 |
rs149934184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194946 | GATACAACTTTTTAA[A/G]CTTTATTAAGATACA | 221178 |
rs149935190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282202 | GGACGTGTGTCTGCC[A/G]AGCACCTGGCACATG | 221178 |
rs149940637 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033468 | AGAGAGGTCTCTCTG[C/G]TACCTTCCCCCACCC | 221178 |
rs149943400 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202687 | AATACAGACGGAAGA[A/G]AGTGAGAACTGTCTT | 221178 |
rs149945784 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095436 | CAGAATAGGGGAGTT[A/T]AATTTAACGGGTACA | 221178 |
rs149963777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997484 | TAATTTGAGATTTAT[C/T]CATGTCTTTCCATGT | 221178 |
rs149993979 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | SPATA13 | GRCh38.p7 | 13:24297553 | TGGATGAGATGGAGC[C/T]TGTGGACCTGGGGGA | 221178 |
rs149997882 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120608 | TTTCTCATGTGAAAA[C/G/T]GGGGGACAGTAGTAT | 221178 |
rs150004294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276027 | AATTGGAACTGTTGC[A/G]CACTGTTGGTGGGAA | 221178 |
rs150005183 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210726 | TTTCAAGATTGCTTT[A/G]TCCGTCTGGAATCTT | 221178 |
rs150005676 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119406 | TTGATATTGAGGGAG[-/A]GAAAAAATCATTGAC | 221178 |
rs150013878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084757 | CAGTGCAGTGGCTCA[C/T]ATCTGTAATCCCAAC | 221178 |
rs150017186 | in-del | -/AA | 0.0547457 | 0.156127 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086527 | AGAAAGGATGAATTC[-/AA]AAGACAAGTTCGATG | 221178 |
rs150022221 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174487 | TTTCCCTCACAGCAC[G/T]GCTTTCGCTATATTC | 221178 |
rs150032860 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987791 | CAACCCCTGGCAACC[A/G]CCATTCTACTTTCTG | 221178 |
rs150034405 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075874 | CCTTTATTGATGTCT[C/G]TCTCCTGGGAGAAGA | 221178 |
rs150055493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270724 | GGGAACGCATACAAC[A/G]TCAAAGCAGTGAATA | 221178 |
rs150068595 | snp | A/C/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169947 | GTCTTGGAGGAGAAA[A/C/G]CAAGAACTCTCCCTG | 221178 |
rs150071865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236074 | AAGTAGTGAGGGGTG[A/G]GGTCGGGCCTGCAGC | 221178 |
rs150104604 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155446 | GAATACTGCTTGTGA[A/G]GGATGGCTCTGGTAA | 221178 |
rs150106992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091726 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 221178 |
rs150113068 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245833 | GGCTCAAGCAATCCT[C/T]CTGCCTGAGCCTCCC | 221178 |
rs150123503 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057874 | CCAGATTCCCCTCCT[C/T]TCTTTTGATTTCAGC | 221178 |
rs150125126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144416 | ATGAAACTAACATCA[C/T]TCAGCACCTTCTGTG | 221178 |
rs150128993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207949 | ATAGAGGGTAGTTGT[A/G]TTGAGAATATCTGGC | 221178 |
rs150170524 | snp | A/G | 0.0295122 | 0.117835 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052866 | CCTGCCCACCACATT[A/G]TTTATACTACATGTC | 221178 |
rs150177682 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203436 | AGAAAGCCTCAAAAG[C/T]GCTAGCTACATTTTG | 221178 |
rs150183321 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237153 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 221178 |
rs150187563 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049210 | CAATACCGTTGTGCC[C/T]AGCATGACAACATTT | 221178 |
rs150191178 | in-del | -/TCCT | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142163 | GAGGGGTCTTATGTA[-/TCCT]TCCTTCTCCCAGTGC | 221178 |
rs150200121 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290460 | GCACCCCTTCTCGCC[A/G]GCCAGATAACGCTTG | 221178 |
rs150234704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233839 | AAGCTGCGGAATCCC[A/G]AGTCTCCTCCAGCAC | 221178 |
rs150250567 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197068 | GTGGCCAAATAACAA[C/T]CAGAGGGCACCTGAG | 221178 |
rs150261749 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012791 | GCCACAGCAATGCCC[A/G]GAACACCACCCTGAG | 221178 |
rs150264602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185171 | AAGTTCCCCTGTGAC[A/G]TATTTTTGTGCTGCT | 221178 |
rs150270574 | snp | A/G | 0.000735036 | 0.0191567 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249603 | CCATTCTCTGACTAC[A/G]GCCAGCTGGCCAGCC | 221178 |
rs150273310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000107 | GGTGAGGTAAGAAAC[C/T]TAGTGGGAGGGTTAG | 221178 |
rs150314855 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122037 | AAGCTCTTCACTACA[A/C]TCACACAGCAGGAAA | 221178 |
rs150320416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277680 | CACATCAGCAATTTG[C/T]AGTTCAATTGGAAAT | 221178 |
rs150326467 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027490 | TTATTAATATTTCCA[A/G]AGAATAAACTTTTTA | 221178 |
rs150331575 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087817 | CTCCTGCTCCTCCCC[A/G]GAGCTGCTGGACACA | 221178 |
rs150333842 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176283 | CATGTTGAACTTAAA[C/T]AGATCTGGTGTCAGT | 221178 |
rs150349345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990129 | CCTGCACCTGGTCAC[C/T]ACCATCTTGTTGAGA | 221178 |
rs150390154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269081 | CAGGTTTTTTGGAGC[A/G]ACAGCAGCAGCGTGA | 221178 |
rs150402737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021153 | GAGTTTCCACAGAAA[A/G]GAAGGTATTAGGAGA | 221178 |
rs150403487 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167892 | TGAGCAACTGCATCG[C/G]CCCTGACACTGAGCT | 221178 |
rs150445569 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278890 | TCCTTCCTTCCTTCC[C/T]TCCTTCCTTCCTTCC | 221178 |
rs150445754 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263458 | TATACAGTCATCCCT[A/G]GTTGTCTGAGGGGGA | 221178 |
rs150454818 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016441 | CACGTTTCTCAAATT[C/G]TTGCTGGAAGAATTG | 221178 |
rs150457583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164548 | GGAGGAAGCATTTGC[A/G]TGAGGTATCCTCTGT | 221178 |
rs150462396 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231438 | GATCAGTGCTTCCTT[C/T]CTTGTTAAGGCTGCG | 221178 |
rs150474130 | snp | A/G | 3.4562e-05 | 0.0041569 | missense | SPATA13 | GRCh38.p7 | 13:24290877 | AAGTATACCACACAG[A/G]AACACGGGTGAGGGG | 221178 |
rs150476137 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065912 | TTAACAATTTGACTT[G/T]TCTTGGACCCCTTAA | 221178 |
rs150480791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280848 | CCAGCAAAGCATACT[A/G]GACTAGGTGACCTCC | 221178 |
rs150481845 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219324 | TCACGTTGTTCAGCT[A/C]AGGAACAAAATACTA | 221178 |
rs150493032 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031653 | TTGAGCTTATGTCAG[G/T]CACTGTAGATGCAAA | 221178 |
rs150500855 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305254 | CCCACCTACCTCCAC[A/G]GACTTCCTAACAGAG | 221178 |
rs150501959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238882 | ATTAGATTCTTGTAT[A/T]CCTCAGTGAAAATAA | 221178 |
rs150503845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986769 | AGAAAGAGCATCGGG[A/G]CCATACAGCAGTCAT | 221178 |
rs150513186 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050978 | GTTGTGTTACCTGAG[C/G]GTTTTCCAGCTGTTT | 221178 |
rs150515306 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138972 | ACATGTTATTTCCTA[G/T]GGCTGCTAAAACAAA | 221178 |
rs150518345 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200450 | ACCATGTATGCACTG[C/T]GCAACCTGAAACGTG | 221178 |
rs150552471 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300932 | AAAGATGTAAAGGTT[C/T]GGTACATCAGGCAAG | 221178 |
rs150558473 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045056 | AAATAAAATCCAGGG[C/T]GGCGGAGTTTGTAAG | 221178 |
rs150569838 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260203 | TGGAGGAAATGACCT[C/T]AAATGAGGCTTTAGG | 221178 |
rs150574659 | snp | C/G/T | 0.00637247 | 0.0561273 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287286 | CCCTCCTCAGCCCCC[C/G/T]GAGTAGCTAGGGCTA | 221178 |
rs150582894 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161027 | TCCCAGTGGACTGCC[A/T]CGGGGCTTCGGGATG | 221178 |
rs150612649 | in-del | -/T | 0.290977 | 0.246619 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022937 | TACACTTGAATCTTC[-/T]TTTTTTTTTATTATT | 221178 |
rs150619329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228837 | AATAAATATTATAAT[A/G]TACTTTCAATAGGGA | 221178 |
rs150636381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123767 | AATGCCTTGTATATG[A/G]GGCTTTGGATTCTTC | 221178 |
rs150640204 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190808 | TTAGAATATTACATA[A/C]ATTTAATTGATAAAG | 221178 |
rs150652769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029159 | AAACTCCTGGGCTCA[A/G]GTGATCCTGTCACCT | 221178 |
rs150652967 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089261 | CATGGTTTGCTGTTC[A/G]TATGGTCATAACCCA | 221178 |
rs150655520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178549 | TAATAAATGAGCTTA[C/T]TCTGTGCCATGCATT | 221178 |
rs150660503 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243487 | GCAGGCTTTCCAGAG[G/T]AGAGGCAGAGGTTTT | 221178 |
rs150662314 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992036 | TGCTAAATATTTCAC[A/G]TGGATTATTTTATGT | 221178 |
rs150665951 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291744 | CTCTGTCTTTATTTT[-/A]TTTATTTTTTTATTT | 221178 |
rs150680021 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025818 | TTCTTTCTTTCTTTT[C/T]TTTTTTTTTGAGACG | 221178 |
rs150705376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084180 | AGCAACAAGCGAGAC[A/G]AGAGAAGAAAGCAGC | 221178 |
rs150707373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206185 | ATCCATCTGACAAAG[A/G]TCTAACATCCAACAT | 221178 |
rs150708532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182297 | GTGTTTGTCTTTTTT[A/G]TTTTGCTATAAAGGA | 221178 |
rs150711978 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270547 | TCACTGAAGGCTCTC[A/G]GCAGCACCTGATGGC | 221178 |
rs150720868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080600 | GGACAGGCCGCACAC[A/C]ACCTAAGAAGGTAAC | 221178 |
rs150722269 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169487 | GTATTTCTGACTGCT[A/G]TCCTCACTGACCGGC | 221178 |
rs150723396 | in-del | -/TGGGAG | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217750 | GCGTGTTGCTTGAGC[-/TGGGAG]TGGGAGTTGGTGCTG | 221178 |
rs150727601 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236728 | TAGAATGGCTACTAT[-/A]AAAAAAATAACAAGT | 221178 |
rs150737295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982666 | ATGAAATATTTTTCA[A/G]TGCATTATCTTCATT | 221178 |
rs150738256 | snp | C/T | 9.90393e-05 | 0.00703632 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286846 | GAGGCCAGCCAGAGC[C/T]GCCACAGACACTGTG | 221178 |
rs150763906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265495 | ATTATTTCCTGTGAA[A/G]GACTCTCCCATCCCA | 221178 |
rs150774499 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077402 | AGTACATGTGATCAT[A/G]CTGGAACGAAAGAAC | 221178 |
rs150775874 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165808 | CTTGAGTGTTAATGC[A/G]ACAATTCAGTCTCAT | 221178 |
rs150780064 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232653 | GTCAAGCAATCCTCC[C/T]GCCTCAGCACCACCC | 221178 |
rs150785351 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041177 | CAACCCACAGTAGCT[C/G]AGAACCACACTGGAA | 221178 |
rs150788533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067568 | AATATCAAATTTAAA[A/G]TCCATTGAGATGGAA | 221178 |
rs150798239 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282165 | GGCTAAGCATGATGG[G/T]GGGGGGTGGGAGTCT | 221178 |
rs150810719 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033230 | AGAACTGCTCAAAAC[A/G]TAGAATTTCAAAAAT | 221178 |
rs150829474 | in-del | -/T | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257639 | TGGCAAATATAGTTC[-/T]TTTTTTGCAAGCTAG | 221178 |
rs150834546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257031 | CTTACTCCATCACAG[C/T]CTACCTAAGCTCCTA | 221178 |
rs150843060 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008387 | TGGCCAGGCCCTGTC[A/C]CTGGGGCTGGCTGAT | 221178 |
rs150845844 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157092 | CTAACCCGGTCTAGA[C/T]CTTAAGTTACTTCCT | 221178 |
rs150850951 | snp | C/T | 0.00320279 | 0.039889 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223426 | GCTCCCCCTTAGCAC[C/T]GGGACCAGCATGTGG | 221178 |
rs150858020 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059649 | TTCAAGTAAGTATAA[A/G]TGTGTCCATTTTATA | 221178 |
rs150860564 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269390 | TGTATGTATGTATGT[A/G]TGTATGTATGTATGT | 221178 |
rs150862172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120145 | CCTCAGCCCTGTCTC[C/T]CTCTGTTCCTTCCTC | 221178 |
rs150870333 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210255 | TTGTTGTTTCTTTTG[A/C]TATGAAAAGCCTTTT | 221178 |
rs150874550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026147 | TGCAAATATATTCCC[C/T]TCAAAGTATGATTTT | 221178 |
rs150916645 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116178 | AGGCTGGGAAATCCA[A/G]GATCAAGGTGGCAGC | 221178 |
rs150944233 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292200 | GTGCATGCACAGAAG[C/G]CTTTGTGTGGTTATA | 221178 |
rs150946792 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039606 | GGGCCTCGAGGGGTC[A/C/G]TTTCTTAGTTCTTGC | 221178 |
rs150954375 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191780 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 221178 |
rs150963318 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280290 | AGGTCTAACTTTTCA[A/G]TAGACTCCTGTTAAT | 221178 |
rs150969690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005555 | AAAAAGGGCCATTAT[A/G]CAGCTTTCTTCCCTG | 221178 |
rs150971730 | in-del | -/TCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278950 | CCTTCCTTCCTTCCC[-/TCTT]TCCTTCCTTCCTTCC | 221178 |
rs150979133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245746 | ACAGGCACATAAAAC[C/T]GTGCCCTGCTATTAT | 221178 |
rs151020645 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085554 | CAGCTCAAAGGAGGA[C/T]GTCCGAGGGACCCTA | 221178 |
rs151021908 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001344 | TGTGTCTCGTGGGAA[A/G]GCTGCAGGAGTGGAG | 221178 |
rs151023735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183569 | GGCCCAACACAAATT[A/C]GTAAACTTTCTCAAA | 221178 |
rs151026069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117472 | ACCATTTAGACAATA[C/T]TTCATCAAATATATT | 221178 |
rs151032794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271897 | CAGGGATGTGGTTAC[A/G]GCTTCTGTGTCTGGT | 221178 |
rs151041713 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022797 | GCAGGAACATAAGTT[A/T]TCCTGGAATTAGACT | 221178 |
rs151042445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082418 | AGGGTAACACTGATG[C/G]AGAATTCACCTTGAG | 221178 |
rs151044359 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170898 | TGGGAACAGAAGAGT[A/G]TTCTTTGATGGGATT | 221178 |
rs151049508 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237126 | ACTTTCTGAGGCCGA[C/G]GTGGGTGAATCATGA | 221178 |
rs151051819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983998 | AACAAGATACCTATG[G/T]CAGAGTATTTCAGGC | 221178 |
rs151073763 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173518 | CCCCCAACTTTTTTT[-/T]TTTTTTTGGCCTTAT | 221178 |
rs151094873 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141677 | GCGCCTGCCACGCAG[A/C/G]GGGTATGGAATGGTT | 221178 |
rs151101993 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233594 | GAAAGTAGCTTTTTA[C/T]TTTAACAATGGAATC | 221178 |
rs151106371 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042581 | TCTATGCCCGTGCGC[A/G]AACTCACTTCTCAGA | 221178 |
rs151115018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130778 | CAGAACCTGCAAACA[C/T]GCTATTTTCCTGGAC | 221178 |
rs151157839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010264 | ATTTTTATATAAACA[G/T]TGGGGCAGAGGAAGC | 221178 |
rs151168536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158056 | AGATGTTATGTGGAA[A/C]AACAACAAAAAAAGC | 221178 |
rs151171301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225699 | GAAATTGGGAGGGTT[A/G]TAGTGTTACAACTTT | 221178 |
rs151180127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060904 | ATTAGCTGGGCATGC[C/T]AGTGCATGCCTGTAA | 221178 |
rs151184743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121928 | ATGATCGGGTCCCAT[C/T]TCCTGGGGTTGTTGT | 221178 |
rs151201518 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027424 | AGGCGTGAGCCACCA[C/T]GCCTGGCTGCCTTTT | 221178 |
rs151208960 | in-del | -/TGAA | 0.0566069 | 0.158427 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979243 | AAACTTGATTCCCAC[-/TGAA]TTCAGTCAGGATCTC | 221178 |
rs151219849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221071 | TTATTTACAGTCAGG[G/T]TCGTGAGGCCCAGGA | 221178 |
rs151236254 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150710 | GCTGGGGATTCAGGC[A/C]GGCTTTTGTGTTGCA | 221178 |
rs151239162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241567 | GTGGTTGTTCCTCAG[C/T]TTGCCTAAGTGATGC | 221178 |
rs151241760 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306798 | GTCCATTCTGTATGA[C/T]TCGCTAACCTACTTT | 221178 |
rs151254255 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052360 | GCTGAGCAGCGTTAA[C/T]GAGATCCCATCGCTA | 221178 |
rs151255703 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202899 | TAGGAGTGGAGAAGT[C/T]GACAAGCAAACAGGA | 221178 |
rs151289020 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145491 | GAGTCCACAGAGGAC[A/G]TAAACCGAGTGAGCT | 221178 |
rs151296528 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301935 | AGGTACTGTAATCCC[C/G/T]GTTTTAGGGATTGGG | 221178 |
rs151315433 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016124 | GGACTCGGGACTCTG[C/T]GTATGTCTTTCTCAG | 221178 |
rs151324168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163821 | GGTAGGTTGACCTCT[C/T]TGTTTGCTGCTGGAA | 221178 |
rs180674432 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136217 | TGGCTTATGCCTGTA[A/T]TCCTAGCACTTTGGG | 221178 |
rs180675575 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166037 | AGTGCTCTTCTGTAA[C/T]GTATAAAAGTCTTTC | 221178 |
rs180680904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184182 | GGTACCTGGTGCTGG[C/T]GCTTGCTGAGAATGA | 221178 |
rs180684162 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119787 | GGAAGCCTGGGAGAG[C/G]TTCCCAAGGCCCAAG | 221178 |
rs180691551 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24145034 | TAGAGGAAAGGGACA[G/T]TGTGAATATAGTTAG | 221178 |
rs180693975 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101534 | TAACCATTTTTAAGT[A/G]TACAGTATAGTAGTG | 221178 |
rs180713498 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190279 | ATATATATTATTATA[C/T]ATAATATATAATATT | 221178 |
rs180714043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045047 | CCTCTCTAAAAATAA[A/G]ATCCAGGGCGGCGGA | 221178 |
rs180720358 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066029 | GCCTGAAGCATTTGC[C/G]TAATAATGCCAAGTA | 221178 |
rs180721115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156496 | GCAAAATGCTTTCCT[A/C]TCTGTGCCTCAATTA | 221178 |
rs180724127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175076 | TGGCCCGGGGTATTG[G/T]TCCATCTTGATATAT | 221178 |
rs180730767 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126986 | TTTAAATCCTTTCAC[A/G]TTTGTTATCTAATGT | 221178 |
rs180737692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007467 | GGGGCTTTTTCTTTT[A/T]TCTTTAGAGGTGCAG | 221178 |
rs180740346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023009 | GCTCGTTACATAGGT[A/G]TACATGTACCATGCT | 221178 |
rs180742952 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110285 | TGGTCAAGGAGTGAG[C/G]AAGGGAGGGGAGGAT | 221178 |
rs180745443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072568 | CCTCTCCAGCCCCTC[C/G]TGCTCACACACAGCT | 221178 |
rs180748826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091459 | AATGCCTTTGAGATA[C/T]GGCTGTTAGAACAGA | 221178 |
rs180755305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036840 | GATTGAGATGGCACA[A/G]TCTCGGCTCACTGCA | 221178 |
rs180758698 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084057 | GGATTATAGTTTAAC[A/G]AGCGTTTTTACTCCT | 221178 |
rs180768834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057780 | CACTGCAGTCAGGTG[A/G]GAGGGGAGGTACAGA | 221178 |
rs180833081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229980 | ATGTACCAAATCAAG[A/G]AAGGCTTCATAAGGG | 221178 |
rs180847339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247349 | TTGTGTCTTTGTTGC[C/T]ACTGATTAACTGTGT | 221178 |
rs180851023 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207386 | ACTTAAAATAAAAAT[C/T]GGAAAGAAAATAAAA | 221178 |
rs180865538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266077 | TCAGTCTCCAGAAAT[C/G]CTCCTAGAGAGGTCA | 221178 |
rs180866131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251922 | TCTGACCGTTTCCAG[C/T]TAACCTGAGGCAGCA | 221178 |
rs180870335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290227 | TTGAAATGGGCATTT[C/T]TGAGGAAAACCTGAC | 221178 |
rs180875207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302037 | GCCAAGGCAGCATGA[A/G]CTCCAGACTTCCATT | 221178 |
rs180876577 | snp | A/G | 0.00164242 | 0.0286096 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286176 | CCATCCCGCCCACTC[A/G]TGCTCTATGCTGAGC | 221178 |
rs180898070 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242577 | TAAATCCATTGTCTT[C/T]TCATCGTAAAATGGG | 221178 |
rs180903996 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283815 | TGCTTGGCAGCATTG[C/T]TATCTATATTTATGT | 221178 |
rs180904285 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24180445 | AATCTCAAAATTTGT[C/T]TTCTTTTCAAGATTG | 221178 |
rs180907433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262450 | TAAAATAAGGCAGTA[A/C]GAATTCTTGATTCAT | 221178 |
rs180909605 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161805 | TTCAGCTCTTGTTCC[C/G]ATGGCTTCCCATAGC | 221178 |
rs180911219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141663 | ATCCTTGCAGCCCAG[C/T]GCCTGCCACGCAGGG | 221178 |
rs180924425 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270726 | GAACGCATACAACGT[C/G]AAAGCAGTGAATAAG | 221178 |
rs180940563 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305512 | CTTCAAGAATGGAAG[A/G]CTCAAGTATTCTCAT | 221178 |
rs180951522 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985389 | ACGGCTGATGTGGGG[G/T]CTCAGTGGCCAGAGG | 221178 |
rs180964532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211721 | CAGGATTATCTCATC[C/T]GGTGGCACTGACGAT | 221178 |
rs180971409 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994344 | CAGTTCTCAGATGGA[A/G]CTTCAGCTATTGTAT | 221178 |
rs180985728 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232771 | CCAGGCTGGTCTCGA[A/G]CTCCTGAGCTCAAGT | 221178 |
rs180993769 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194255 | TAAATGTGCAGCTAA[A/T]ATCGTCCTGAATGTT | 221178 |
rs181011059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013308 | CTTCCACAGCATTGC[A/G]TGCCCACTGCCAGCC | 221178 |
rs181141322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281938 | ATCATGACAGCCCTG[C/T]CTGTGCTTGGCAAGG | 221178 |
rs181164303 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298004 | AGATTGTCTCATTGA[A/G]TCCCTATGAAGTGGT | 221178 |
rs181175659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073994 | CCTGATTCTTATTTC[A/G]CATTGTAATTTACAC | 221178 |
rs181193542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100492 | TGTCTCCCTCTCTCA[C/G]CTATTTCCAGTAGCA | 221178 |
rs181199124 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111463 | CCGAGGCTGAAGTGC[A/G]GTGGTGCAATCACGG | 221178 |
rs181199173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156099 | TTGATGAATACTTGG[A/G]TTGCTGTCACCTTGT | 221178 |
rs181200047 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083834 | AACTGCTCATTTCCC[A/G]GCTGCTCCTTCCCTT | 221178 |
rs181200513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135677 | CACTCCTGCCTGGGC[A/G]ACAGAGCAAGAATCC | 221178 |
rs181202778 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092446 | ATAAAAAGAGATAAT[A/G]GTTTATATTTTAGAA | 221178 |
rs181205369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049968 | CCCTCTGCCTCCCCG[A/G]TTCAAGCAATTCTCC | 221178 |
rs181211390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118224 | CACCTGACATTGCTC[A/T]GTGCCTCAGAGCACT | 221178 |
rs181211860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070124 | TGCTTGCTTGGAGTA[C/T]AGAGTTCAGGAGCAG | 221178 |
rs181229003 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988085 | AGTAGCTGGGATTAC[A/T]GGCACCTACCACCAC | 221178 |
rs181230212 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009861 | TGTCTTACCTCCCTT[C/T]CATCCTGGCCTAAAT | 221178 |
rs181233951 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065278 | TCTTAAACTTCCCCC[A/G]TGTGCTGAGCTTCAG | 221178 |
rs181235867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006719 | TTGCAATGAGGCCAG[C/G]CTACACATGGTGGAG | 221178 |
rs181239103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028789 | TGTGTGTAATCTGCT[A/G]TTTAACTGTTGCTTT | 221178 |
rs181250751 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044615 | TTACATTGTTTAATG[A/G]TCGAATCGGGGTAAT | 221178 |
rs181265771 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022534 | AAAACCTTCTGATCT[C/T]TTACAAAATAGTGTG | 221178 |
rs181285056 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018344 | TTGCAAAAGATCGTT[G/T]TTTCCATCTTAGCAT | 221178 |
rs181301104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088594 | TTTTAAAATGACATA[A/G]TAAACACATCTCTTT | 221178 |
rs181337914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984412 | ATCATTTGCTGAAAG[A/G]ATTATATGAGGTTGC | 221178 |
rs181358336 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189716 | TATTATATATAAAAG[C/T]ATATATAATATATAA | 221178 |
rs181359541 | snp | C/T | 0.00532129 | 0.0513062 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232255 | TTCAGTGTTCCTGGG[C/T]AGGAGAAGGTGGATG | 221178 |
rs181367114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203666 | GCTTAAATTTCACGG[G/T]TTCTTCAATTCTCAA | 221178 |
rs181367296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251320 | CACCCTGGCCGGGTT[G/T]GTGGCCTTGTCCTGG | 221178 |
rs181367559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172553 | CATGAGATTTAGGTC[A/G]GTGTTTTTTTCTTGG | 221178 |
rs181386244 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041271 | TTAATTGTTATATAA[A/G]TTATTTGGATTTTTA | 221178 |
rs181386950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225972 | AGGCTGAGAAGAGCT[A/T]TATTGGGTGACTGAA | 221178 |
rs181392125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181265 | TCTAAATGTATTTAA[C/T]ATATGTGCTGCTGAA | 221178 |
rs181393692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162977 | TACCTGTAGGACAGT[A/G]CATGGAGAAAAACCT | 221178 |
rs181400548 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096175 | CTTGTTCTGGAGCTA[A/T]ACCAAAGAACAAAAC | 221178 |
rs181415799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262091 | CACATCAGAAAATTC[C/T]GTTTCTTGATTTAGA | 221178 |
rs181420789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152793 | TGCAGAGCCACTCCA[A/G]GTCCTTATCATGGAG | 221178 |
rs181430254 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133043 | GCACACCTGGAGATG[A/G]TATGACAGTTGAGGC | 221178 |
rs181430714 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123094 | TAAATTCTTCACTAT[A/T]TTCACAGATCATTTT | 221178 |
rs181431852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115470 | GAGCGTGAACCCTAT[C/T]GCAAACCGCGCATGC | 221178 |
rs181443103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062757 | GCACCGTGTCTGCAT[C/G]TGTCCACATGCATTT | 221178 |
rs181451789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193735 | TATCAGAGGAGCAGG[A/T]CTTCTTCTGGAGGAA | 221178 |
rs181467763 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161066 | CCAGCTGCTTGGCCT[C/T]TGCTTCCCCCGCCGG | 221178 |
rs181473655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172249 | TCAGTGTTATTCTCC[A/G]ATGATACTAATACTC | 221178 |
rs181482392 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132502 | CTAGGACCCCAAGCC[G/T]CAAATTGGGGGTAAA | 221178 |
rs181487663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079857 | CTTACTTGACTCTCC[C/T]GTGAGGATGGGGATA | 221178 |
rs181495119 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202684 | CAAAATACAGACGGA[A/G]GAGAGTGAGAACTGT | 221178 |
rs181503056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141917 | TGCCATTTAACTGGG[C/T]GTGCAAATGGAGTCA | 221178 |
rs181503990 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213699 | CATTTATTTTAGTAT[A/G]TTACTAATGAACAAC | 221178 |
rs181504471 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115064 | ACAAGGTTTCTTGTT[G/T]GCCGTATATGCTCCT | 221178 |
rs181505668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017283 | TCCGAGAAATAGAAT[A/C]ATTTGCCTGGGCGTG | 221178 |
rs181511120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095426 | GTAGGGGGTGCAGAA[C/T]AGGGGAGTTAAATTT | 221178 |
rs181515709 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040849 | AGTTTTTGAGGATAC[A/C]GATTGTGGTTGGCCC | 221178 |
rs181520561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062193 | CTCTGGTACAGTGTG[A/G]CTGTTTACTAGTGAT | 221178 |
rs181520934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211301 | TTATGTTGAATGGAA[A/G]TGGTGAGAGTGGACA | 221178 |
rs181525720 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241539 | GGCTTTTATAGGAGC[C/T]CCTCCCCTCACAGTG | 221178 |
rs181542270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252703 | ATGTTTTAATTTTAG[C/G]GTTCTTTTGTCGAAA | 221178 |
rs181542341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296748 | CTTACCAGAGGCTTC[A/T]GGCTAGGAAGACCCC | 221178 |
rs181547419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281816 | AGAGGGGCTGGGGCC[A/G]GGCTGGGAGAGGCGC | 221178 |
rs181552321 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271774 | AAATGAATGGGAACC[A/G]TAGATGGCAGCTCGA | 221178 |
rs181561083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141087 | GGCTGAGGCAGGAGA[A/G]TTGCTTGAACCCGGG | 221178 |
rs181566896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257742 | ATACAGTAATACGAA[C/T]TGCTAGCAGGCAGGT | 221178 |
rs181569055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294235 | GGCGAATGCCATACT[G/T]GCATTTCCGTAACTC | 221178 |
rs181573754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105612 | AAATAGGCCTACGGA[A/G]GATGTGCTTTAGAAT | 221178 |
rs181575076 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277272 | ACATGGTGAAACCAC[A/G]TCTCTACTAAAAATA | 221178 |
rs181585774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179805 | TTATTGGCTATTTGG[A/G]TATCTTCAAAGAAAT | 221178 |
rs181591884 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080654 | TCTGAGATTTCATCG[C/G]TGGCCTTGATGTCAC | 221178 |
rs181607821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124082 | GGATTTGTCAGAATC[A/G]TCACCAGCTTCCTCT | 221178 |
rs181611219 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152514 | CACCAGGGAGGTCCT[C/G]CCCAGTGAGGTCTTG | 221178 |
rs181627360 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306667 | TAAATATTTGATACA[A/C]GTTTACTTAGCTACA | 221178 |
rs181637893 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190186 | ATTATATAACATATC[A/G]TATATAATATATATT | 221178 |
rs181643652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189152 | GATCAAGGAGTAATT[G/T]TGACTCTGATGTCTT | 221178 |
rs181649290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207283 | GCTGGGCTTAATACC[A/G]AGGTGATAGGATGAT | 221178 |
rs181660113 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174897 | AAGTTTCCCTTTAGA[A/G]TTCCCCCTTGACTTG | 221178 |
rs181676700 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229364 | AGTTGGGACCCTGGC[G/T]CTATTATTAAAAGAT | 221178 |
rs181696905 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000669 | CCCTGTGGGGAAAGA[C/G]GCTTGTGTTCAAGAA | 221178 |
rs181702156 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240913 | CATTGTTTTAAAATG[C/T]TTAACAAATGACCAA | 221178 |
rs181721554 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24290398 | AGAGACCAGGGTGCT[C/G]AGTTCCAGGGCAGCC | 221178 |
rs181723321 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285785 | ACCTGAGTTCAAGTG[A/G]TTCTCCAGCCTCAGC | 221178 |
rs181771982 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146593 | TAGGCTATAAATAAC[C/G]TCTAAAATGTTCTTT | 221178 |
rs181803981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219669 | CAATTTGATGAGATG[C/G]CTGAAGGCCTGTGGA | 221178 |
rs181805028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225027 | CTATTACCTGTCCTA[A/G]TGTCACAGCACCTGT | 221178 |
rs181814339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246670 | CGAGACCATTCTGGC[C/T]AACATGGTGAAACCG | 221178 |
rs181815541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261751 | CCCACTGGATCCAGT[A/G]GCAGGGAGGAGCTTC | 221178 |
rs181816560 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185257 | AGTGCCCATCACACA[C/T]GATAGGCACTCAGTG | 221178 |
rs181827612 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050343 | ATCTGATAATGCTGA[C/T]GAGTCAGTTTCCGGA | 221178 |
rs181828746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123378 | ACCCAGCAAGCCCTT[C/G]CTCTCATGTAGCCTA | 221178 |
rs181831811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070838 | GCCTTCCGACTCAAA[C/T]CAAAATAGCAGCTCT | 221178 |
rs181832607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106453 | GAAACCATTCCACCA[C/T]TGACATGGGTGGGAA | 221178 |
rs181835995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089062 | TATCTCAAGACAACT[C/G]AATTGGCAGTTTTCA | 221178 |
rs181846583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027820 | GGATCTTAGAAGAAC[A/G]CGTGGTGTAGATTAA | 221178 |
rs181862404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987619 | GACTAATTAGAAGGT[A/G]AAAGCCCCGGATTTG | 221178 |
rs181892211 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24017018 | CAGCCTCAGGAAGGC[A/T]GGAGGTAGTGAGGAG | 221178 |
rs181907051 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978345 | TTTATTATTTCTTTC[C/T]TTCTACTTACTTTGG | 221178 |
rs181916680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999588 | TGGAGTCAGGGAGAT[C/G]TCCAGGCTCAGGGTG | 221178 |
rs181929031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083502 | CCAGGCGGAGCTTGC[A/G]GGGAGAATGGCTAGC | 221178 |
rs181932293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265531 | AGAAAGTGCAGCCCC[A/G]TCTCAGCTGTGGGAG | 221178 |
rs181938850 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236341 | AATAGACATTTCTCT[A/G]AAGAAGATATGCAGG | 221178 |
rs181948821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021647 | AATCTGTGACTGTAT[A/G]CGCCGTGCATTGGGC | 221178 |
rs181953864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044171 | GCAAGCCACACCACA[A/G]TGATGGCCTGGTGGG | 221178 |
rs181955711 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013816 | CTCGAAGGCTTGGGT[A/G]CTGCATACAGTCAAT | 221178 |
rs181957261 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064604 | ACAAACCAGGAAGTA[A/G]GCCCTCACCAGACAC | 221178 |
rs181957737 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24266997 | ATGGTTTAGGTTTTC[A/G]TTGTAGGATTCTTAC | 221178 |
rs181963103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301209 | ATTCCCGTCATCTTT[C/G]TACTTTAAAAGGCAT | 221178 |
rs181966432 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218642 | GCCGCAGGCTGCATG[A/T]GGCCCAGGGAAGCTT | 221178 |
rs181967059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293772 | TGGGTGTGAATGGGC[A/G]TCTCTGAAGACAGCA | 221178 |
rs181974476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184575 | CTTGTTGATTTTTTT[C/T]CTCTCTGATGTGTAA | 221178 |
rs181977517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198383 | AATCATAGGAAGTCT[C/G]TTTATAATAAAGCAG | 221178 |
rs181981916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257050 | CCTAAGCTCCTAATT[A/T]TTTTGTACTTAACAT | 221178 |
rs181992892 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235822 | CAATTGCTCCATCCA[C/T]TACTGAGAACTAGAA | 221178 |
rs181993127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277166 | AAGTTCACCTTGGGC[C/T]GGGCGCGGTGGCTTA | 221178 |
rs181999561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114867 | GGGTTTCTCCATGTT[A/G]GTCAGGCTGGTCTCG | 221178 |
rs182021085 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166641 | AGGGCTCCCACCAGA[C/T]CTATAAATTAGTTCT | 221178 |
rs182022005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078873 | ATCCTGTATCCTCAT[G/T]TACCATGCTGGGTAC | 221178 |
rs182038260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167680 | CAGTTTACACACACA[C/T]ACACTCACTCACTCA | 221178 |
rs182053067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127938 | GTTGGCAGAATGATG[A/C]TGTAATGAACGAACA | 221178 |
rs182061583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198874 | TCTTCCTCAGGGGTG[A/G]TGCAGGACCTTTTCT | 221178 |
rs182069235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010257 | AATCTGCATTTTTAT[A/G]TAAACAGTGGGGCAG | 221178 |
rs182076783 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009569 | GCAGGGTGTGGGATT[G/T]TTCCAGGTCATAGGT | 221178 |
rs182098542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092828 | GCTTTTATACTCCAT[A/G]GACTCCACTGTGTGG | 221178 |
rs182099359 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978696 | AGGTCTCCTAACATT[C/G]TCTATTTGTCTTTTT | 221178 |
rs182118527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250264 | AATAGTTTTTTAGGA[A/G]ATGAGAAAGTATTTT | 221178 |
rs182122953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146847 | AGATTTCTTTACCAC[C/T]GCATCCGTCCCCGCC | 221178 |
rs182124948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047218 | TCTCAGAATAACAAT[C/T]TTAGGCAATATAAAA | 221178 |
rs182127878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086566 | CTGTAGCCTTGGGGA[C/T]TGGCGAGAAGGTGGA | 221178 |
rs182128923 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231116 | CACCCAAGACTAGGC[C/G]ACAGCTGATGGGCTT | 221178 |
rs182129845 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128473 | TGTTGCTCAGAGGTA[A/G]TTAAATGGTGGGGCA | 221178 |
rs182130272 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268140 | ATTGTTAAATTCTAT[C/G]TTAAAGAAGATGGCA | 221178 |
rs182132253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112243 | TCTCCTCTGGCATTG[C/T]AGCAAAGCTGTTTGG | 221178 |
rs182133265 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068232 | TCTCCTGATTTAGCT[A/C]CCCCTTATAAGTGAG | 221178 |
rs182138598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058627 | TCATGGCTTCAAAAC[A/G]GTCTACATAATTATG | 221178 |
rs182149041 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288058 | GTATGAGTGTGTGGC[A/G]AAAGAAGCAGGTCTG | 221178 |
rs182155228 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303784 | GGTGGCGCATGCCTG[C/T]AATCCCAGCTACTGG | 221178 |
rs182191997 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983474 | TCCTGTGAATTTTGA[A/G]CCCAGAGCAGAGAAT | 221178 |
rs182247540 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230465 | CTTTAGTGCCCCGGG[C/T]GGCGGTTGCAGAAGG | 221178 |
rs182248146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248318 | AAGGACCTGCTGTTT[C/G]CCAGGGAATGGCTGC | 221178 |
rs182255863 | snp | A/G | 0.00439744 | 0.0466839 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286402 | CGTCAGAGTAAGTGT[A/G]GGGTGCTTGCAGCTT | 221178 |
rs182257823 | snp | C/G/T | 0.00597646 | 0.0543919 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191600 | CTGCAAGCTCTGCCA[C/G/T]CTGGGTTCACGCCAT | 221178 |
rs182260662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199131 | TGAGCTCAAGCGATC[C/T]GCCCGTCTTGGCCTT | 221178 |
rs182266630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169539 | GCAGACACCTTCTCC[A/G]GACTCTGCCCTGGAA | 221178 |
rs182298331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196935 | AGAGGAGAAAGAGAT[A/G]AATGTGAAATGAGCA | 221178 |
rs182299351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095132 | CAGTGTTATTCCCAA[A/C]AGCCAAGAGGCGGAA | 221178 |
rs182308468 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092105 | TTTGAAAAACTTGTT[G/T]TGGCCATTTTTGCCA | 221178 |
rs182309914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203873 | AACAAATATTTAATG[A/G]GCTGCCATTAGGTGC | 221178 |
rs182314751 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163486 | CCGTTTCACTTTAGC[G/T]GGACAGATCTTTATG | 221178 |
rs182318581 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226639 | TTTGCAGGTATAGAT[G/T]GTGCTTGCCATAGAG | 221178 |
rs182318737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182646 | AAACACCTCCCCCAG[A/G]CCCCGCTTCAACACT | 221178 |
rs182327962 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131419 | AAGCATCTCTACTTA[A/C]CTGACCTGGGCACTG | 221178 |
rs182340427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108386 | GTTGAACTTAACCCC[C/T]AGTGGGACGTGTGCC | 221178 |
rs182340540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127667 | TTTTTGTTTTCTCAC[A/G]AAGCATTGGTAAATC | 221178 |
rs182345323 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989503 | ATGAACTGAAAAAAA[A/C]AACCCAAAATAGCGT | 221178 |
rs182346255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089851 | GCACCAGCAGGTTTG[G/T]TGTTTGGTGAGGGCC | 221178 |
rs182362595 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061291 | TACATTGGTTTAGCC[A/G]TTGTAGAAAGTAATG | 221178 |
rs182365931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030697 | CAGGGGAATTCTTTT[A/G]TCTTGCTACTACAAC | 221178 |
rs182367406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071568 | AGGGAAAACCAGCAC[A/G]CAGAGATGTGACCTC | 221178 |
rs182370213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143900 | TTCTTCTAATGTCCT[C/T]ATCTGCAAAATGGGA | 221178 |
rs182372201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124979 | AACTGAAACTCATTC[A/G]TAGGGTCAGAGCGGG | 221178 |
rs182381612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104258 | TTTTTTTTTGTTTTT[C/T]GGGTTTTTTTGGAAA | 221178 |
rs182383663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075050 | AACCCTTAGGCCAAG[A/G]TTAGAATATGTGAGG | 221178 |
rs182404366 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037243 | GGCATTAGGAGATAT[A/G]CCTAATGTAAATGAC | 221178 |
rs182410829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227501 | TTATTAAAGGTGCGT[A/G]CACATGTTGATAATT | 221178 |
rs182414491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273407 | TGAGAGTTAATATGT[C/T]AGTTTCTAGGATTCC | 221178 |
rs182417463 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190042 | ATATACAATATATAT[C/T]ATTATATAACATATA | 221178 |
rs182418013 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073531 | GGAGTGGCAGTCTGT[C/G]CTCACACACAGGTGA | 221178 |
rs182420626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206166 | GAGAAAATTTTTCCA[A/G]TCTATCCATCTGACA | 221178 |
rs182422607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253359 | CTCTCTCTCTTCCCT[A/G]GAAGGAGACACCCAG | 221178 |
rs182429449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245143 | CCGGCAGCCCACGCC[A/G]GAGTCTGAGTTAGGC | 221178 |
rs182435194 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038060 | GGGATTATAGGCGCC[C/T]GCCACCATGCCCAGC | 221178 |
rs182439213 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307058 | TTTGTATATTAAAAT[G/T]CATTTGCCAAACTCG | 221178 |
rs182455999 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006052 | GGGCTGCAAGCAGCC[A/G]GAGGTGCCTGCTGTG | 221178 |
rs182464010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997213 | TTTCTTCATTTGTTA[A/G]GGTATAATGGGCATA | 221178 |
rs182480706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278196 | CATTTTGTCTTATTA[C/G]AAGTAACAGCTACTG | 221178 |
rs182538874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138485 | ATAAAGGAACTGCTG[C/T]GTTGGTTTTATAAAA | 221178 |
rs182542413 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208630 | TCACCTTCTTGTCCA[A/G]AGGGTTCCCAGACAT | 221178 |
rs182554522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110790 | ACACATGGGAAAGGG[C/G]AGATCTTTCCACCCA | 221178 |
rs182556528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209834 | TTAGTTTTCTGAGGC[A/G]CCTCCATGCTGTTTT | 221178 |
rs182568080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176996 | TCTCAAACTCCTGAC[C/T]TCAGGTAATCCACCA | 221178 |
rs182573781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237042 | TGTGTACATATACTG[C/T]GGAATATTATTTATG | 221178 |
rs182592778 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145968 | AACAGGCATAGACTG[C/T]GGGGGCCAATCTGTC | 221178 |
rs182609497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986530 | GCCTCTCAAGGATCA[A/G]CCCCTTGGCCTTTTA | 221178 |
rs182611393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013986 | AGTCTGGAGTGTGCT[A/G]GAGTCAGAGCCTCCA | 221178 |
rs182613824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215668 | TCTAATTAAGCTGTG[A/G]ATGTAAAAGCTACAT | 221178 |
rs182616549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037936 | TTTTTTTTTGAAATG[A/G]AGTCTCGCTCTGTCA | 221178 |
rs182618522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253562 | TGTGGAGAATAAAAC[A/G]TCATGCAAAGTTTAC | 221178 |
rs182625880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058936 | TAGACCTGTAAGCTC[C/T]AGGACAAGAGCCATG | 221178 |
rs182644975 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189828 | TATTATAAATATATA[G/T]AAAATGATATTTAAT | 221178 |
rs182647767 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995555 | ATGAAATCTCCATAT[C/T]GACTGAGGTTTTCCC | 221178 |
rs182652057 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174218 | GAAAGCGGTCCATTT[C/T]GTTGAAGTTGTCAAG | 221178 |
rs182655817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154264 | TGTCCTGGCCACATA[A/G]TAACCAAAAGTAAAA | 221178 |
rs182658437 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134461 | TGCTACATAGAGGTC[A/G]TATGGATGCCGAGAG | 221178 |
rs182662878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153415 | AAAGGAACTTGTTCT[C/T]GTCAGGTAGACAAGG | 221178 |
rs182670607 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014657 | TAACAAAATAGTGTA[A/C/T]GTCTTCTCCTAAAAT | 221178 |
rs182687044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058995 | GTTTTGTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 221178 |
rs182697903 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991640 | ATGTTCATAGCAAGT[C/G]CAGCACCGTGCATAT | 221178 |
rs182722040 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291692 | TGTTGTTTGGATCTC[A/G]GCTTCTCCTGAACAA | 221178 |
rs182737606 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134083 | AGCAAATGGTCCAAA[C/G/T]GGAGTGACAAGGTAG | 221178 |
rs182737805 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042685 | AGAGCTTCTCAAAAT[G/T]CATTGTGCATGCATA | 221178 |
rs182741773 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116538 | CATCTCCTGCACTTG[A/T]TCTTCATTATCTCAG | 221178 |
rs182741960 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063975 | TCTTCACTGTGTGGC[C/G]TCACCGCCTCCAGTG | 221178 |
rs182749070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081761 | GACCACTGGATGTTG[C/T]TGGCAGTCCTGGAGC | 221178 |
rs182749261 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097322 | AGAAGCTAAATAATT[G/T]CCCCAAGGTCATGCA | 221178 |
rs182784042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299744 | GGAGAAGGCAGGGCC[C/T]CAGCACCCAGCCCTG | 221178 |
rs182800353 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157916 | ACTTCATTTGCCCCA[C/T]ATATAAAATGAGAAG | 221178 |
rs182809638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071199 | TGTAGAGGAGACAGC[G/T]GCATCTCAGTGGAGT | 221178 |
rs182823470 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121299 | ACTATCAGAGGTGAG[C/T]GCACCACAAAGTCAG | 221178 |
rs182833315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011424 | GGTCTGGCTTGCTGC[C/T]CTCCCCTGGAGAATG | 221178 |
rs182834413 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233764 | ACAGACTAGTTAAAC[C/T]GGCAAATTATGTACT | 221178 |
rs182838521 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033926 | TACTAAACAGAAAAG[A/G]AGAAGGCAATGGTGT | 221178 |
rs182841640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089688 | AGTTGTCCTACAGGA[A/G]GTATTTGTCATTTAT | 221178 |
rs182843057 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24053922 | GAACTCACAAAGGAA[A/G]TGTTATTATGGGGTG | 221178 |
rs182844151 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258604 | AGCCTGGGAGGCAGA[A/G]GTTGCAGCGGGCCAA | 221178 |
rs182844337 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220636 | CATCCAAATGTAACC[C/T]CCAGCTCCTCTGGCC | 221178 |
rs182848553 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192435 | TCCTGCCCCTTCAGT[C/G]TCTGTGCCAGTTCCT | 221178 |
rs182866021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154036 | ATTAGAAAACTGAGG[A/C]TAAGACAATACCAAG | 221178 |
rs182870312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264403 | TCTTACAGACAAGGT[C/T]AGGCCTTAGAAATAT | 221178 |
rs182887350 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209243 | TTTTAAAGGTGCTAT[A/C]CCCGTTTCTCTATTA | 221178 |
rs182893545 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230823 | ACATCATTAGGAAGG[C/G]CCTCGCTTACAGCTG | 221178 |
rs182895804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046655 | CTGTATAGATGTCCA[A/G]TGTATAATACCGAAA | 221178 |
rs182896746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192007 | AAAAGAAAAATACAC[A/G]GCAAAGTGAGATGGA | 221178 |
rs182897046 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233991 | TACCTGTAGTTTTGA[A/G]CTTTCCAGTGGCTCA | 221178 |
rs182910465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133314 | TTCATCTGGTAGAGA[C/T]TGTGTAAGCCCAGTT | 221178 |
rs182911036 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249032 | GCGCCACCGCGCCCC[A/G]CTAATTTTTATATTT | 221178 |
rs182921206 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008277 | CACCTGAATTCACTC[C/T]TGAAGGTTGTGGGCT | 221178 |
rs182929375 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990900 | ATTCAGAGTCTTGGG[A/T]TGAGACCCTGAGTGT | 221178 |
rs182946056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173163 | GCTCACTGCACCCTC[C/T]GCCTCCCGGGTTCAA | 221178 |
rs182946955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234237 | TGATAGGAAGCAATA[C/T]CATAATATATTCTTC | 221178 |
rs182953831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157672 | GAGCTCCTCAAAGAA[A/G]AAAAACTGAAATGAG | 221178 |
rs182957426 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176559 | CTTTGATTAATGGGA[A/C]CAGGCAAGTCCAAGG | 221178 |
rs182957965 | snp | C/T | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254066 | AGATTGATTTGAAGG[C/T]GATTGCATTAGTCCA | 221178 |
rs182959844 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216103 | GGTTGCTGTGAGATT[A/G]GAGGAAGAGGAGCTC | 221178 |
rs182970480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137843 | ATGTGCGTCATCAGA[A/G]GTTAGGACATAAGAC | 221178 |
rs182972323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275630 | TCTTGTTTACAAGAT[C/T]GTTTCCAAAAATGGC | 221178 |
rs182975621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299184 | GTCATCTGTAAGTCA[A/G]AGTGTTTGGATTCCC | 221178 |
rs182989971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292114 | CTCACGCCCTTGTTC[C/T]CTAGCTATATGATCT | 221178 |
rs183010927 | snp | G/T | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307435 | AGGAGCTGTGCTAGT[G/T]GCCCTGCTCACTCGC | 221178 |
rs183053075 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979434 | CTGGGAAATTTTAAA[A/G]GAGATGGGAAACGAC | 221178 |
rs183108275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163183 | AGGAGGATTGCTTGA[G/T]CCCAGGAGTTCAAGA | 221178 |
rs183123980 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124479 | CCAGGGCAGCTGCAG[A/T]GTATCAGACTTTCTC | 221178 |
rs183130779 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196403 | TGTAATAAAGCCTTA[A/C]ATTATATAACATTCA | 221178 |
rs183164861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284756 | GGCAGCTCGTCTTTT[C/T]AGGTAAGGAACAGCA | 221178 |
rs183173412 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002393 | TTGACAAACGAATTC[A/G]AGTAGGAGGGAAATG | 221178 |
rs183179135 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026212 | TTCTTAATGTATTCC[A/G]TCTTTTTCCTTTTAT | 221178 |
rs183182034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295606 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 221178 |
rs183189224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067923 | TGGCAAGGTTGGTCT[C/T]GAACTCCTGACCTCA | 221178 |
rs183207702 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979922 | GGAGGGATGCTGAGA[C/T]AGGCAAGTGGGATTT | 221178 |
rs183238838 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106542 | TGGCCAAGCCTGTAG[A/G]TGCATTGCTCAGCAG | 221178 |
rs183260740 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237639 | TAACAGTGTGAATGT[A/G]CTTAATCCCACTGAC | 221178 |
rs183269548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221308 | TGTTTTCCAAGACCT[C/T]AGGGCAGAGGCCTGA | 221178 |
rs183273627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278545 | AGTCTTCCAAAGTGC[C/T]GGGATTACAAGCATG | 221178 |
rs183281821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001547 | GGCCGGGCTGGCTGC[C/T]GTGTCTGTTAGGGTC | 221178 |
rs183282587 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258751 | ATAAATGTCTTAGTG[A/G]TAAATCCAGCATGCT | 221178 |
rs183289834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295041 | TTGAATTTAACAGTC[A/G]ACTACTTTATACCCC | 221178 |
rs183290854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033606 | TCACGAAGGTTGTGG[A/T]TCCTTGCCCAGCCTG | 221178 |
rs183306994 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070904 | ACTATGTCCTCAGCT[A/C]TCCCAGGTTTCCAGG | 221178 |
rs183345133 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284436 | AAGGCCAAGGCAGGT[A/G]GATCATTAGTGGTCA | 221178 |
rs183378430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116802 | GCTGATGTTTGGAGA[A/G]AGGGCCTTTGGGAGG | 221178 |
rs183385780 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142478 | TCAGTTTTGGATTGT[C/T]TGATGTTTTCTCCTG | 221178 |
rs183388285 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157352 | CACCCAGGCTGGAGT[A/G]CAGGGGCGCGATCGC | 221178 |
rs183401068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214407 | CCAAGAAAGGTGTCA[C/T]GCCATGAGAATAATT | 221178 |
rs183407480 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181491 | CCATAATCTTTTTTT[A/T]ATTAAAATTTGTTTT | 221178 |
rs183417901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085643 | CTTTACCTGACTTTA[C/T]TCACTTCCATGTGGC | 221178 |
rs183422144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244437 | GTTTGCTTTCACTGT[G/T]GTTTCAGAAAACATT | 221178 |
rs183428275 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205323 | GAAAGCCAAGCCATG[A/G]AAGAATTTCCATTTA | 221178 |
rs183437030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998000 | TTGTTTCTGGTCTTG[A/G]GCTATGATGAGTAAA | 221178 |
rs183438190 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046038 | AAAAATACAAAGCAT[G/T]GCATGTTCTGTTTCA | 221178 |
rs183438420 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136837 | TTATTTTATTTATTT[A/T]TTTTTTTTTTGAGAC | 221178 |
rs183440001 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120262 | GTTATTGAGAAATTG[G/T]AGTGTAACTACAGGG | 221178 |
rs183440730 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187263 | CAGTCATCCCTGCCT[C/G]AGAGTGACACATGAG | 221178 |
rs183441318 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015698 | CAGCCAGGACACCCC[C/T]GGCCTTCCTGATCCT | 221178 |
rs183443791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108174 | CTCAAGCCCTTTTAT[A/G]GGGTTACTAATCCAT | 221178 |
rs183446831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066547 | GTCTTTGAGCTGTGC[A/G]TCAAAGCAGAGGCAT | 221178 |
rs183449447 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101906 | ACTTGGGTTGCTTCC[A/G]TCTTTTGGCTATTGT | 221178 |
rs183453538 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038090 | CTAATTTTTTGTATT[G/T]TTTTAGTAGAGACGG | 221178 |
rs183458948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222003 | TTTTTAGTAGAGATG[A/G]GGTTTCATGATATTG | 221178 |
rs183481926 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089265 | GTTTGCTGTTCGTAT[G/T]GTCATAACCCATGAG | 221178 |
rs183491318 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120543 | TCTGGCTACACCACT[C/T]ACTAGCTGCCTGGCC | 221178 |
rs183512758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186462 | AACATCAGCCATAGT[C/T]CAGAAAAACTGATGA | 221178 |
rs183516488 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085938 | AAGGCAGAGAAGCCA[C/G]AGAGGGTTTCCAGGG | 221178 |
rs183519981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200249 | GGCACTCCTGGGTGG[C/T]GCAGAAGGATTTGAA | 221178 |
rs183535543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980680 | CACTGAAACCTCTGC[C/T]TCCCGGGTTCAAGCG | 221178 |
rs183540191 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052315 | AGGCTGAGGCCAGAG[A/G]ATTGCTTGAGGCCAG | 221178 |
rs183544864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222247 | TCCTTCCCGCCTGTG[C/T]CTAGGTGGCCCTGTG | 221178 |
rs183562240 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188055 | AATTAAAAGTGATAC[G/T]CCAGGCCAGGCGTGG | 221178 |
rs183564826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010783 | TCTTGGCAAGCAAGG[C/T]AGGGCCAGTGCCTTG | 221178 |
rs183567324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202041 | TAGTAGCTCATTTCT[C/T]CAGCCTGGGGGACAG | 221178 |
rs183572121 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262999 | TTTTTTATAGATTCT[A/C]TGGGCTGCAAATTTT | 221178 |
rs183586646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131273 | CACGTATGGGCATAT[C/T]TTGTCTTGACCAGCT | 221178 |
rs183589574 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114269 | GGGGTCTGTCCAATC[A/C]GATTGTGAATCTTTC | 221178 |
rs183595730 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259937 | GAGCCACCACACCCG[A/G]CCTGAGTTGGATTTT | 221178 |
rs183604796 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170582 | CCCTCTGCAGAGTAC[A/C]TCTCTGTTGTCCTCA | 221178 |
rs183617263 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190013 | ATAATAATATATTAT[C/T]ATATAACATAATGAT | 221178 |
rs183626147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127374 | GAGTTGACAACCAGC[A/G]TCATTTCCTTCTCTC | 221178 |
rs183629169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110558 | TACTGCCTCCTAAGG[C/T]GGTGGAGAAGCAGGG | 221178 |
rs183633919 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044501 | CTCCCAAAGTGTTGG[G/T]ATTACAGGCATTAGC | 221178 |
rs183642678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166424 | GAGCAATTAGGGAAG[G/T]AGCTGACAAAGGAAA | 221178 |
rs183645972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184193 | CTGGCGCTTGCTGAG[A/G]ATGACTTATTTTGGA | 221178 |
rs183650958 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24226851 | AAGACCTAGAAAGTA[C/G]GACTATCGCAGAGTA | 221178 |
rs183658829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145063 | AGAATGAGCTGGTAC[A/G]CTATTTCTGAAGTGG | 221178 |
rs183660380 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304776 | GTGGACCATCATGCC[A/G]CTCGGCACGTCCTGA | 221178 |
rs183671618 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987073 | CAGGCCTACCCCATA[A/G]GCAGTGGATTGATAT | 221178 |
rs183699242 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170125 | TCAAATATCTGCAGG[A/G]GGATAGGTCAAATCA | 221178 |
rs183710189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238317 | GTGCACCACCATGCC[C/T]GGCTAATTTTTATAT | 221178 |
rs183715620 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200770 | GCCTCATGACTGTTG[C/G]TCACCTCCGGGTCAT | 221178 |
rs183723233 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267624 | TTAACCAAAAAAAAA[A/T]TTTTTGTAGAAAATG | 221178 |
rs183737534 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103471 | GCCTGGGCAACAGAG[A/C]AAGACCCTGTCTCAA | 221178 |
rs183756254 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245463 | ATTTCAATTTTGTAT[A/G]TTATACTGTAACTAA | 221178 |
rs183757604 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217509 | AGTGAAATAAGACAA[A/G]GCTTCTGCCTATAGA | 221178 |
rs183764427 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228175 | CTGGAGTGCAGTGGC[A/G]TAATCTCGGCTCACT | 221178 |
rs183769251 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265013 | GGTTTTGTGTGTTCA[A/G]GTCCACATTGCTCCA | 221178 |
rs183770563 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198241 | CTTGTGATCTGCCCC[C/G]CTTGGCCTCCCAAAG | 221178 |
rs183786656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080940 | CTCCTGGAAACACAC[A/G]TACCTCCTAATAAGT | 221178 |
rs183788987 | snp | A/T | 0.000118017 | 0.00768079 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24300402 | ATTTCTAAATGCAGG[A/T]ATGGAAATTTCAGAA | 221178 |
rs183795717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054755 | GGAGAAAAGGTTAAG[A/G]AGGATATGCATTTTT | 221178 |
rs183812171 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303087 | GCAGCTGAAGCCACC[C/T]CTGCTGATGATGAGC | 221178 |
rs183859515 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288259 | GGATTTAAACCCAGG[C/G]AGTCTGCCCCAGAAC | 221178 |
rs183863662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021426 | TGAGCCCAGGAGTTT[A/G]AGGCTACAGTGAGCT | 221178 |
rs183876361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043741 | GCATGGCCTGCTGGT[C/T]GTGAAAGGTCACATT | 221178 |
rs183880736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064373 | CACAGTGGAGAAACC[C/T]GGCTGCAATGGACTA | 221178 |
rs183889205 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985860 | TGACTGAAGAGAGGA[A/C]AACAGCCAGCGGTCC | 221178 |
rs183903029 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016147 | TTTCTCAGACACCCC[C/T]GAGACCTGCCCGGAA | 221178 |
rs183905128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987898 | TTCACATAACGCAAC[A/G]TTCTTAAGGCCCAGG | 221178 |
rs183906827 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026068 | TCGGCCTTCTAAATA[C/T]CTTTTCTTTTTACTG | 221178 |
rs183965240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062997 | TGGGGGAGACTCAGG[A/T]CAAGGGACACACTTC | 221178 |
rs183974353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035534 | CTTTACAGGCCACAA[A/G]GACAGGTTGGTTTTC | 221178 |
rs183974820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275999 | GAAACTACGGTTGGT[G/T]AGAATGTGGAGAAAT | 221178 |
rs183982357 | snp | C/G | 0.00319098 | 0.0398384 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096718 | CACCTAAGAACAGAG[C/G]GGGGACTGGAAAAGA | 221178 |
rs183984791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293182 | TAAAAGAAGAGAGAG[C/G]TATATATTTTTTTCT | 221178 |
rs183986066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207326 | CCACCATGGCATACG[G/T]TTACCTAGGTAACAA | 221178 |
rs183989044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246926 | GCATCTTACTAGGCC[A/G]GGAGAAGAGAACTTA | 221178 |
rs183992273 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229600 | TTTTAAGACAGGGAC[A/G]TTAAGGTCGGTTCTT | 221178 |
rs183997965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992378 | TGATACTAAGTCCTG[A/T]AGTAAAGCCCAACAT | 221178 |
rs184000622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128926 | TTTCTCACCCAAGAT[C/G]AAGTAATGATTGGTT | 221178 |
rs184005871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265569 | GTGATGTCCACAGGT[C/T]CTGGCTGTGTCACTC | 221178 |
rs184047672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169649 | GGCACAGGTGCCCAG[C/T]GTCGCTTCTCAGCGG | 221178 |
rs184050783 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059249 | GTGCTGGGATTACAG[A/G]TGTGGCCCACTGCAT | 221178 |
rs184067523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007858 | ATTACATATACTCAA[C/T]GCATGGTGAGACTTA | 221178 |
rs184077016 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092930 | GTTTTGGTGTTTGGC[A/G]TCTTCTCATTAACGT | 221178 |
rs184079945 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090759 | TATAATAGCTGACTT[A/C]AAAACTTAAATCCAA | 221178 |
rs184100338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039749 | TGTGACTGGGGTTGG[G/T]GGAATTCTGTAGTTG | 221178 |
rs184110681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057491 | GTCCTGTGACTGCAT[C/T]CATATGGGACTGGGT | 221178 |
rs184111067 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126552 | GTGTGTGTGTGAGAG[A/G]GAGAGACAGACTCCC | 221178 |
rs184115492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072468 | TGGCAGGGCTGGACA[A/T]GGGCCATCCTGTTCT | 221178 |
rs184117625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109989 | ACTCCCATTCCATGT[A/G]AGAACTAATTTTCTT | 221178 |
rs184130221 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077481 | ATCCAAAATGGGGGA[A/G]GAAGGGAGTGGGTGA | 221178 |
rs184135492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013195 | TTCCTGTCTCCCCAC[A/G]CGTGCTGCACTGTTT | 221178 |
rs184138701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036494 | ACTGGTTAGGTGCAC[G/T]GTAGAATCTGGAACA | 221178 |
rs184145459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999453 | GAGAAGATTTGGCAT[A/G]TTAACAATATTGAAT | 221178 |
rs184156248 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175334 | CTTGAAATCATAGTG[C/T]CTAGCAAACATAGGG | 221178 |
rs184158045 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147041 | CCAATAGGCCTCTGG[A/T]TGAGTTTATTATTTT | 221178 |
rs184194944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992795 | TGGGGACATGGCCAC[A/G]TTTGGCTCCACAATG | 221178 |
rs184196137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012475 | AGAGACAAAGGCTGT[A/G]CCTACTGTCTCCAAG | 221178 |
rs184211186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075343 | TCGGTTTGGCAAATA[A/G]TAGTCACTCAGTAAA | 221178 |
rs184215787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180075 | TGTATTTGAGAAACT[A/G]TTGCCTAATCCAAGG | 221178 |
rs184221189 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270198 | TTGTAGATAATTTGG[A/G]AAGTATAGAAGAGTA | 221178 |
rs184242228 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289784 | CTATTACTACTTAAC[C/T]GCTAAAGGATTTCAG | 221178 |
rs184255281 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24305010 | TCTCTGCTAGAGTTG[C/T]TTGTATGTACAGCAA | 221178 |
rs184262025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060730 | TCTGTAAGGAACTTA[A/G]GCAAATTTAGAAGAG | 221178 |
rs184262631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239466 | TTGGGATGCTGAGGC[A/G]GGTGGATCCCTTGAA | 221178 |
rs184264038 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279983 | TTGAAACCTCTCTTG[A/T]GATTAACCTCAGCCA | 221178 |
rs184266327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211302 | TATGTTGAATGGAAG[A/T]GGTGAGAGTGGACAT | 221178 |
rs184280691 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977753 | TTTCTGTCTTTCAGA[G/T]AATCTTTTTTATCTA | 221178 |
rs184288430 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016595 | CTTCCTAAGCAGGCT[C/T]AGTGTCCAGGGCCCG | 221178 |
rs184326960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141396 | AGGTCACTTGTTGAC[A/G]TTGGGCCTTGCTAAT | 221178 |
rs184359598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154962 | TCCCAGGTTCAAGTG[A/G]TTCTCATGCCTCAGC | 221178 |
rs184361759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044173 | AAGCCACACCACAGT[G/T]ATGGCCTGGTGGGCC | 221178 |
rs184364953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194009 | GTAGAGGTTTCTTAC[C/T]TTCTCAACCATTCAA | 221178 |
rs184371270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091617 | GGAGTCTGAGACCAG[C/T]TTGGCCAACATGGTG | 221178 |
rs184397858 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261081 | CTGCCTGGGAGGACA[C/G]AGCCTGGGCAACTGG | 221178 |
rs184399503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232287 | CTGCCAGGAGAGGAG[A/G]GGAATCCTGGACTTT | 221178 |
rs184402153 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083133 | AGGCATTCATTCCAG[C/T]CTTGAGGTGCTCACC | 221178 |
rs184403288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129893 | GTGGGGGATTAATAA[C/T]CTTAGGACCTCGCAG | 221178 |
rs184404354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038741 | GCTGCATTTGGCCCA[G/T]GGGCTGGAGTTCTTG | 221178 |
rs184411744 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059578 | GGAGAGGCTATTATA[C/T]GCTGAGGACAGATAC | 221178 |
rs184411988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009729 | AGATGAAGCCTCCAG[G/T]TAGCAGGCTTCAGAG | 221178 |
rs184413326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113502 | CCAGCTGCTCGGGAG[A/G]CTGAGGCATGAGAAT | 221178 |
rs184416529 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076406 | GCAACTGGGCAAGGA[C/T]GAGGGGAACAGACAA | 221178 |
rs184423652 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117112 | AAGATAATCAGTATG[C/T]TGCACTTTCTATAAA | 221178 |
rs184438134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094571 | TTTATGCTTAAAATG[C/T]TTTTAAAAATGTTTT | 221178 |
rs184454050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174600 | TCACTTTTTTGAGAC[A/G]AAGTCTTGCTCTGTC | 221178 |
rs184456878 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293702 | TTGGGGGCTCTGTGC[A/C]CATTATTTTGGCAGT | 221178 |
rs184484381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174439 | GATTTGAGATGGTTC[C/T]TCTTTTCTTATATGA | 221178 |
rs184490641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135016 | CATGAGATGCAGGGA[C/T]GAGATGGCCATCTAC | 221178 |
rs184491407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099924 | GAAGAAATGCAAAGA[C/T]GCCATTTCTCTAAAA | 221178 |
rs184506226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206480 | GAGTATAAATTAGTT[C/T]AGCCCTTGTGGAAAA | 221178 |
rs184510097 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064840 | TTCACCTGTGGGGTA[G/T]GTATTTTTTTCAAAA | 221178 |
rs184511814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155766 | TATTGTTATGCAACC[A/G]TCACCATCATCCATC | 221178 |
rs184515070 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183026 | GAGGATATCTGCTTA[C/T]ATATATTCCTCATTC | 221178 |
rs184516897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197654 | TAGTAGTAAATAGCA[A/G]GTCAAAATAAAGTAC | 221178 |
rs184519256 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083563 | TGTTGGGTTTCCCTA[A/C]GTTTCCAAGCCTGTT | 221178 |
rs184527596 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256498 | ATAATATAAAAAACT[A/C]TCCAAATTAAGTAGT | 221178 |
rs184529581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281190 | GACCAAGGCTGTGGA[A/G]CGCTTTCTTCTGCCT | 221178 |
rs184534095 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117665 | TAAGTGCCTTTAAAA[A/G]GAGAAAGAGAAATTA | 221178 |
rs184535391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240808 | CAGCTGTGTTTTTCG[C/T]ATCTTTTATCATCCA | 221178 |
rs184541499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296677 | ACTCTTGGAGGCTCC[G/T]TTTGGGTCAGCTGCT | 221178 |
rs184564703 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098735 | AGATCGAGACCATCC[C/T]GGTCAACATGGTGAA | 221178 |
rs184566332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193381 | CATTGTTGACACAGG[C/T]GGTGGCCATGTTGTT | 221178 |
rs184576754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178588 | GGTATTATTATCTGT[A/T]TAAGAACAAATAGAG | 221178 |
rs184579303 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160096 | CTGGGAAACATGTAG[A/G]TTTAAAAATCCCTAC | 221178 |
rs184589985 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202467 | GCTTGGGCGCTTTCT[C/G]CAGGTTGGATGCCAG | 221178 |
rs184596589 | snp | C/G | 0.000918906 | 0.0214152 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224739 | GGAGTTGTCAAGTTG[C/G]TGTTTACCAAGTTCA | 221178 |
rs184631511 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24235053 | GGAACATGGTAAATC[A/G]GGTTAATAGTAGCTT | 221178 |
rs184641619 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198195 | AGACGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 221178 |
rs184645217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235459 | TTCAAGCAAGAAATG[G/T]TGTGATAAAGAATTG | 221178 |
rs184676271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276966 | GAACTGCAAATTGCT[A/G]TTTCCCCATCAGCAA | 221178 |
rs184690349 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255624 | CCATCTCTCAGCAGC[A/T]TCTCTGGCCTAGAGA | 221178 |
rs184696121 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211090 | AAAATAAATTCAACT[A/G]ATTTTTCCATGTTGA | 221178 |
rs184702917 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24231621 | TGGGTGGATACCTAG[A/G]GGTGGAATTGCTAGG | 221178 |
rs184709802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285834 | TACAGGAGCCCACCA[C/G]CACGCCTGGCTAATT | 221178 |
rs184710881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269814 | GGCTTGTCTCAAACT[C/T]CTGGGCTCAATTGAT | 221178 |
rs184719549 | snp | A/G | 0.000119494 | 0.00772868 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288988 | AAAAGTATTACTTCT[A/G]TATTTTGCAGGGCTA | 221178 |
rs184731609 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183741 | TTTATAATGTTCTCT[A/G]TGGGCTAATGGTGGC | 221178 |
rs184751408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144687 | CAGCAGCCACCGAGA[A/G]AGGATCCCACCTTTC | 221178 |
rs184784198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177916 | GGCTGGAGTATGGTG[A/G]TACAATCATGGCTCA | 221178 |
rs184794108 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216848 | TTGAGGTCAGGAGTT[C/T]GAGACCAACCTGGCC | 221178 |
rs184797128 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157304 | CTTTTTTTTCTTTTT[A/T]ATATATTTTTTTGAG | 221178 |
rs184803859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998613 | TTTTCTTTTAGGGAT[C/T]GTGATTTTTTGCTGT | 221178 |
rs184817858 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982490 | AAAATAAACTTTACC[G/T]GACTGATGAAAACTA | 221178 |
rs184835546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251571 | AGTTGCCACTGGGCT[C/T]CGGTGCAGCCTGCAA | 221178 |
rs184836208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005861 | ACAGCAGCATAGCTG[A/G]CATTTTTTTCCCTTC | 221178 |
rs184886743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009892 | AACTTTTTCAGGTTA[A/G]CTTTGGAATGCCCTT | 221178 |
rs184888840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988814 | CTTTGTTCATTTGTC[A/G]GTCGGGCTGTTGGGT | 221178 |
rs184892855 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979441 | ATTTTAAAGGAGATG[A/G]GAAACGACCCCGCCT | 221178 |
rs184893136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098408 | TAATTAAGACTTAAA[C/T]GTGGCAAAACCCTGT | 221178 |
rs184905669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028914 | CAATTTCCCCTGTTT[A/T]TTTAAACATGAAAAT | 221178 |
rs184941351 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295940 | AAACCCAAGCAGGCA[A/C]CCTGGCTTCAAAGTC | 221178 |
rs184942564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064107 | CTTTCTCTTGTCAGT[A/G]TTCACTGCACCTGTT | 221178 |
rs184951803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981723 | GCGGTGATAAGCCTC[A/C]TGTCTCACGGCCAGT | 221178 |
rs184970352 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020090 | AGCACCAAGCCTCAC[C/T]GACAGCCAGACTTAA | 221178 |
rs184979272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006430 | GGTGTCAGACAACGA[C/G]AAGACAAACATGTTT | 221178 |
rs184984421 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071617 | TGTAGTATGGAGCTT[G/T]TTCCTTTGGTGTCTG | 221178 |
rs185009910 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082823 | CAGAGCGAGACTCCG[A/T]CTCAAAAAAAAAAAA | 221178 |
rs185012956 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036085 | TTGTTTCTGATGGAC[A/T]AGTTCTACTAATATT | 221178 |
rs185016027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104605 | TCCTTCACTCATAGT[A/G]ACAATGAGAGGGGCA | 221178 |
rs185023875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087611 | AGTGAACAGTGGGGC[A/G]AACTCAGGCATTACA | 221178 |
rs185032980 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088873 | TGGCTCCAGGAAAGC[A/G/T]CAAGCAAGGGCTCCT | 221178 |
rs185039645 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069187 | GTTCAATAGGAATAG[A/C]ATTAAATCTATAAAT | 221178 |
rs185039676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158659 | TTCACTGAAACCCTG[A/G]AAAAAATATTTTTTA | 221178 |
rs185041241 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043000 | AATGAACCCTTTCGC[A/G]ATGTGTGTCTTAGTG | 221178 |
rs185042178 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040457 | AATTCACAGCACCGC[C/G]CTTGACAGGAAACCA | 221178 |
rs185044669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139682 | TTGGTAAGTTAGGAA[G/T]GTGCTCTGGGTTTAT | 221178 |
rs185057938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050091 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 221178 |
rs185058200 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121987 | TTAGAGTAGATAACA[G/T]GAACCACTTCTGGAA | 221178 |
rs185058266 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061434 | ATGCTCATTGTAGTG[C/G]TGTTCAACAATAGCA | 221178 |
rs185065665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070308 | CGTGGCTGACCAGGG[C/T]TGCAGCATTTCTCTG | 221178 |
rs185074292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005255 | GAAAACTGTTTTGAT[A/T]CTTAAATTTTTACCG | 221178 |
rs185084259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084109 | GGAGAAAGAGAGAGC[C/T]GTGACTAGAATTGTA | 221178 |
rs185085804 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055541 | TAACCATGCATTCAC[C/T]GAGAAACCATGTTTT | 221178 |
rs185094361 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022233 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 221178 |
rs185102945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045598 | CACTGTAAACAATAC[C/T]AGGCTCATGACAAAG | 221178 |
rs185111613 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090550 | CCATCCAATCCACCA[C/T]GTCCTACAGACTACT | 221178 |
rs185115071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066136 | GTACCTTTAGGTTAC[A/T]CGTGGACCAAGGTAA | 221178 |
rs185117979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246077 | GCAGGGTGCGTGTCA[C/T]GTAAGTGTAAAACCA | 221178 |
rs185122020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144034 | ACGTAGAGTGGGGAG[A/G]ACAGAGAGCCTCCCA | 221178 |
rs185123315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101553 | AGTATAGTAGTGTTA[A/G]CCCTATGCACATTCT | 221178 |
rs185129701 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23983887 | ATGAAATGGCAACAC[C/T]GTGCAGATGGCAAAG | 221178 |
rs185134884 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23985434 | TGCTGTGGCTTCTTT[C/G]CTCTTACCTGGGTCT | 221178 |
rs185136900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007636 | AATTTTTTGTATTTT[C/T]AGTAGAGACAGCTTT | 221178 |
rs185138639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108786 | TCCTTGGGATTTTTC[A/G]GAAAGATTGGCGCCC | 221178 |
rs185140804 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023081 | TCTCCCAATGCTATC[C/T]CTCCCCTCACCTCCC | 221178 |
rs185188234 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122698 | CTGTATCAACTGTTA[A/C]ATAATTACGAAGGAG | 221178 |
rs185189395 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190134 | ACATAATAATATACA[A/G/T]TATATATTATTATAT | 221178 |
rs185192925 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148591 | ATAACCAGTGTGATA[C/T]GTTAGGAGTTTAATA | 221178 |
rs185218221 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152838 | TGAAGCAGCTTTCTC[G/T]CTCTCTCTCTTTCTC | 221178 |
rs185223227 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265331 | ACGTTCAATGCCTTT[C/T]AGGTTCCTCTGGAAA | 221178 |
rs185223851 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048952 | ACTCAAAGAAAAAAA[C/T]GACAAAACAAAACAA | 221178 |
rs185224228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133080 | AGGAGCCAACATTAG[C/T]AATGGATTCCCACGT | 221178 |
rs185227487 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228923 | AATAATCGTTGAAAA[A/T]TTTTAAGCAGTCTAA | 221178 |
rs185245681 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189749 | TATTATATATAAAAG[C/T]ATATATAATATATAA | 221178 |
rs185249593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203800 | CTCTCCCACAGAAGG[A/G]TAAATTTACTTTGCA | 221178 |
rs185250035 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125550 | CAGTTTCTAAAATTC[A/G]CCAACCAAGTGGTTT | 221178 |
rs185252239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088028 | TAACAATTTTATAAT[A/G]TCTCAACAGCTGCTT | 221178 |
rs185263842 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172710 | CTCTGTTCTTTTGAT[C/T]TATATGTCTATACCT | 221178 |
rs185273495 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164088 | ACCAAATGTACATGG[C/T]TTTCTTGAGGGAAAC | 221178 |
rs185289809 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | SPATA13 | GRCh38.p7 | 13:24297501 | AAGAAGGACCTGCTG[C/T]GCAGGGACATGCTGT | 221178 |
rs185295834 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140125 | CATCTCTAAGGCTCC[G/T]GCCAATGCTAATAAC | 221178 |
rs185306765 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104855 | GTTTTATTCATGCTC[A/G]CTCCCCCAGCTCCTC | 221178 |
rs185343220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069688 | TTCCAGGGGTGCATG[C/T]CTAACATGCATTATT | 221178 |
rs185361258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261898 | AGCTGTGTTGATGGT[G/T]TTCTCATTTTATAGT | 221178 |
rs185373835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028196 | CTTAGGCTTGTTCAG[A/G]TACACACACATACTT | 221178 |
rs185376754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268485 | TGTAAGAGGCTGGGC[A/G]CAGTGGCTCATGCCT | 221178 |
rs185391183 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281833 | GCTGGGAGAGGCGCC[A/G]CTGGCAGCACGTGCA | 221178 |
rs185416333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266738 | CCCAGTTCCAGTGAG[G/T]TAGTGGTATCTTATC | 221178 |
rs185417011 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193248 | TGAGGAAGGGGAGTT[A/G]CAGGGGAAATGGACA | 221178 |
rs185419518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171744 | CAAACCTGGTGATTG[A/G]TTACGTGAATAACAA | 221178 |
rs185426719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294269 | ACTTCAGGTGCCTGT[C/G]CTCTCCTGTCCTTTC | 221178 |
rs185427116 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220653 | CAGCTCCTCTGGCCC[C/T]CTAATTCCTCCATTA | 221178 |
rs185427391 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302156 | CCCTGTCAAGTTGTT[C/G]TCATAATACCCTCCT | 221178 |
rs185431612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131867 | GGGAAGGCAGATTAG[A/T]GAGGTAGGCAGCTGT | 221178 |
rs185450925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231315 | TTGTGTCTATTATTT[A/T]ACTTTTCTGGACATT | 221178 |
rs185471284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291130 | TCGTGAGCTGTGCCA[C/T]GAGTGCATGGCGGCT | 221178 |
rs185489731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186372 | AAGGTCAGAGGTTTA[C/T]GATATGTCAGGGATA | 221178 |
rs185491427 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307316 | GAGTAAGAGGGATGC[A/G]GAAGGGAGCAGTGGG | 221178 |
rs185496231 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199676 | CTTGCGTCTTGTGAT[C/G]TAAGCTCTACTTCTG | 221178 |
rs185498184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247393 | TCACGTCACTTCTTT[A/C]GGTCCCAGTTTTCCT | 221178 |
rs185545676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151250 | GCATTCAGGTTACAT[C/T]AGGACTTTGAAAGAC | 221178 |
rs185547788 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210840 | TGACTTTCAGTAGTA[C/T]GGACATTTTAATGAT | 221178 |
rs185557299 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111803 | CATGATAGCTATTTT[A/G]AAATAGATTGTTAGA | 221178 |
rs185566824 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092467 | TATTTTAGAAGCAGA[A/G]GAGTTAATAGGAGCC | 221178 |
rs185575550 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188781 | TTTTCTAGCTAGAGA[C/G]GAGAAGTCAGTGTCT | 221178 |
rs185584374 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190242 | TATATTATTATATAA[C/T]ATATCATATATAATA | 221178 |
rs185584966 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251046 | AAGAAATCTAAGGAA[C/T]GTATAAAGCAACTGG | 221178 |
rs185586769 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074501 | CATTTAATTGTACTC[A/G]TGATGACTGTCCCTT | 221178 |
rs185588803 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146625 | ACAGGGCACTAAGGA[A/G]ATGGAAATGCACAGC | 221178 |
rs185597268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127948 | TGATGATGTAATGAA[C/T]GAACAGCATTTACAG | 221178 |
rs185601265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156150 | TATGAAAGTGGGTGT[A/G]CAAATATCTGTTCGA | 221178 |
rs185603746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174898 | AGTTTCCCTTTAGAG[G/T]TCCCCCTTGACTTGT | 221178 |
rs185633708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984792 | CAGCCAAAAAAGACT[A/G]CCTATTTCTGAGAGC | 221178 |
rs185691150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095249 | CAAAAAGAAGAAAAG[C/G]CTGTTACATGCTATA | 221178 |
rs185712511 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027343 | TTTCACCATGTTGAT[A/C]AGGCTAGTCTTGAAC | 221178 |
rs185741178 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987264 | TGTGGTATTTCAGAA[A/G]ATATTTTCATGGCTA | 221178 |
rs185754678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241608 | GCCTGGACAGGTGGA[A/G]AGAGCCAGGGAGTGG | 221178 |
rs185756383 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24300791 | GGTGTTAGCCACAAG[A/G]TCACGCACATCCCCA | 221178 |
rs185768085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226345 | ATGAATTAGGAACAT[C/G]CAGTTTGGTACCTGT | 221178 |
rs185775934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120427 | TGCCTGTGTCCCTAT[C/T]AGGCGCAGCAGCAGT | 221178 |
rs185784091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262121 | AATTGATATTAATCC[C/T]CAACATTTAGGAAGT | 221178 |
rs185784622 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102676 | ATGGGGTTTCACCAC[A/G]TGGGCCAGGCTGGTC | 221178 |
rs185788612 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078904 | TGTGGACCCAACAGT[A/T]TGGGAGATGGGCACA | 221178 |
rs185795629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175802 | ACGGATCTAGGTGTC[A/G]TTTTTCTTCTCCCAC | 221178 |
rs185799955 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218911 | GAATTTCAAATTTAA[A/G]TTTTTATTTAAAAAT | 221178 |
rs185800426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014268 | ATTAGGACACAAGTC[A/G]TATTGGATTAGGCTC | 221178 |
rs185809083 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157522 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 221178 |
rs185814018 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037940 | TTTTTGAAATGGAGT[C/T]TCGCTCTGTCACCCA | 221178 |
rs185814858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198536 | ATCTCCCACAGAGGC[A/G]TTGTTGAGTTTGGCT | 221178 |
rs185814885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137041 | TTCACCGTTTTAGCC[A/G]GGATGGTCTCAATCT | 221178 |
rs185816275 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114882 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCTG | 221178 |
rs185817912 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058954 | GACAAGAGCCATGGT[C/G]TGTGTATTGTTTTTT | 221178 |
rs185834863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066991 | CCTCACAGTTTTAGA[A/G]CCCAGTGCCTTTCTC | 221178 |
rs185840197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009387 | ATTCTGAGCCAAATA[C/T]GAGTGACCCATGAGC | 221178 |
rs185843257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085786 | TTGCTTCTGCCAGGC[A/G]AGACCCAGAGTTTCA | 221178 |
rs185857041 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048192 | CTGGGTATCACTCAG[C/T]CCAGTCAAGTGGACA | 221178 |
rs185874463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115590 | CCCTTCATGTCCATG[A/G]AAAAATTGTCTTCTA | 221178 |
rs185916692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013890 | TTGTTCATGAGGTTA[C/T]TGGGAGCAGGTAATG | 221178 |
rs185917820 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23995513 | TGGCAGGGGCCCTAA[C/T]TGGCAGCCGTTTTTA | 221178 |
rs185918599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080752 | CTCATCTTCTGTGCC[C/G]TATGGCATGTGGAAC | 221178 |
rs185932648 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001580 | TCCCATGAATGCCCC[G/T]GTGTCCTGATGGTGA | 221178 |
rs185949730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041486 | AAGATATCGTCATAT[A/G]ACAGATAAAGCTAAA | 221178 |
rs185965391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252954 | CTGGGTATCCAGTGA[A/G]CGCTTTGAAAATACA | 221178 |
rs185977607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233703 | CAACGGAAAGTTTCA[A/G]AGTATTTCTGAAAGG | 221178 |
rs185979737 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271780 | ATGGGAACCGTAGAT[A/G]GCAGCTCGAGGCAGC | 221178 |
rs185994793 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306709 | ATTGTTGCCTTTAGT[C/T]ATCTCACAGGCACTG | 221178 |
rs186001073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290470 | TCGCCGGCCAGATAA[C/T]GCTTGCGGAAACCAT | 221178 |
rs186015416 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058476 | GTGATTACTGTATAC[A/G]GGACAAAGGAACAGC | 221178 |
rs186040157 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062855 | TTGGAGTGGGTTTTG[C/G]CAGGAAATTACTTTG | 221178 |
rs186040688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213899 | ACATTTTACCTTCTG[G/T]TATTTATTATCTGAG | 221178 |
rs186054128 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013473 | CACTGCTTGGGGACA[A/G]TGCCCAGGATTCTAC | 221178 |
rs186054624 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181481 | TGTCCCTATTCCATA[A/C]TCTTTTTTTTATTAA | 221178 |
rs186056531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195132 | CTGCTCCAGGCTCTG[G/T]CAACCACTGACCTGC | 221178 |
rs186063881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096295 | AAAAAAGAGTGTTAT[A/G]ATAGAAAATAACAAG | 221178 |
rs186066040 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123256 | CAATGGCAGCTTCCA[C/T]TTTCACAGGCATTTC | 221178 |
rs186068260 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258609 | GGGAGGCAGAGGTTG[A/C]AGCGGGCCAAGATCG | 221178 |
rs186068536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018656 | TTTGATGTTTTAGCA[G/T]AGGGTTACTTATTGA | 221178 |
rs186075194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194330 | AGTTAGCGCCGTTCA[A/G]TCATCCTGAGATTGC | 221178 |
rs186098080 | snp | A/C/T | 0.000165243 | 0.00908813 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294883 | GGTAAGTGGAAAGCA[A/C/T]CCCACATGATCCCAT | 221178 |
rs186104076 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095732 | ACCCTCGTTTCCCTA[C/G]AAATTTGGTTCCCTG | 221178 |
rs186110085 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136234 | CCTAGCACTTTGGGA[G/T]GCCGAGGTGAGGTGG | 221178 |
rs186110856 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190289 | TTATATATAATATAT[A/G]ATATTATATATTATT | 221178 |
rs186113299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123623 | CAAAAGTGTCTGGGC[A/G]GCAGTGGTAGGAGAA | 221178 |
rs186120267 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033761 | GCGTGTCCCTCCGTC[A/G]TGTGACAGGTGAGCC | 221178 |
rs186123592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106478 | TGGGAATCCTGGCAG[C/G]TGTTTTGGTTTCCTG | 221178 |
rs186126154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080054 | AATTTTATATTAAAA[C/T]ATTCAACATCACCCA | 221178 |
rs186127256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156559 | GATACTTATGTGCTA[A/G]GATAATGTGATAAAT | 221178 |
rs186130262 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152603 | AGCTCCCACATCCCC[A/G]TCTGTGTGACCAGTG | 221178 |
rs186130539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132585 | AAGTATTTGAAAAGT[A/G]TTAACATTATTAGGA | 221178 |
rs186133353 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089096 | ATGAGGACACCAGTG[C/T]GTCAGGGGACACAAC | 221178 |
rs186135560 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036964 | TATTTTTAGTAGAGA[C/T]GGGGTTTGACCATGT | 221178 |
rs186140961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115088 | TGCTCCTGCAGAGAA[A/G]AGGAAGTGACCGTGG | 221178 |
rs186142836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180935 | TAGATGGTACAGCCT[A/G]CAACACACCCAGGCT | 221178 |
rs186151055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162261 | TTTCTTCCTTGTTTC[C/T]CCATGTTTCTCCCAC | 221178 |
rs186154232 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198918 | GGATTGTATTTTTAG[A/G]ATATATATTACATAT | 221178 |
rs186155816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072650 | CTGGATTTCATTGAA[C/T]CTGCCTTCTGGGCCA | 221178 |
rs186156951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141751 | TTATAGCTAGGGAGC[C/T]TCCCGTGGCTAAGAA | 221178 |
rs186163683 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011087 | TCCTCTGCAACCTTG[C/G]CTTTGGTTTCTCCCC | 221178 |
rs186164165 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994527 | GCATGACTGCAGGTG[C/T]CTTTCAGGCCCTGGA | 221178 |
rs186165672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062387 | GGGGCTGATCAGGAC[A/G]AAGAGAGCTGAGGGC | 221178 |
rs186200295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237015 | TGATGGACAAATGGA[A/T]AAAAAGTATAGTGTG | 221178 |
rs186213537 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278270 | TGAGCCTGCTGCACA[A/C/G]AGCTGTGTGTTATTG | 221178 |
rs186214062 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136001 | CAAAGTGTTCACTTT[C/G]CTGAGCAGAATTAAG | 221178 |
rs186235084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168035 | TCTGCCTCTTGATGA[C/T]GTAATTATTCAACTT | 221178 |
rs186278567 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207405 | AAGAAAATAAAATCT[C/G]TTCCAGTCCCCAGTT | 221178 |
rs186308098 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242582 | CCATTGTCTTCTCAT[C/G]GTAAAATGGGGGTAA | 221178 |
rs186315476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277316 | GGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 221178 |
rs186326103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185322 | CCACAAGGGATTTTA[C/T]TTCTTAGTGAAGTAC | 221178 |
rs186330196 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303444 | CTTCATCAGGGTCCT[C/T]AGTGCAGAGCAACTT | 221178 |
rs186334765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236007 | GTGATTTTTGTATTT[A/G]CTTTAACAGATGAGT | 221178 |
rs186334986 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191743 | TCTTGATCTCCTGAC[C/G]TTGTGATCCGCCCGC | 221178 |
rs186336690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277219 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG | 221178 |
rs186341606 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257314 | AAGCAAAGGACGAAT[A/G]CACACCCGTGCACCA | 221178 |
rs186342100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219986 | AGTCAGACACCTGGT[C/G]CCCCAAATGTACTGC | 221178 |
rs186346214 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258198 | CTACATTGCGCCATG[A/G]CACTCCAGCCTGGGC | 221178 |
rs186353489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293905 | GCGCAGGAGGATTCT[A/C]ATTCATTCCAGCTGT | 221178 |
rs186370780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118598 | AATTTCTGACCCAGT[C/G]GGTCTGGGGTAGGGT | 221178 |
rs186402903 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262595 | GAGTGTAATCCCAAT[C/G]CTTGGGCAAGTCACT | 221178 |
rs186418789 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284344 | AACCACTTCTGACTT[C/T]GTTCCCTAGTTCTTC | 221178 |
rs186453660 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282850 | AATGCAGTCACTTGA[C/T]TTAGGTCCCATGCCC | 221178 |
rs186468060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253421 | TCTAGGACCTCTTAG[A/G]ATAACTAGTCCTCCA | 221178 |
rs186476203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065781 | CAACCATAAATAGTT[C/T]TTTCGACAATGCTGT | 221178 |
rs186487735 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100537 | CCTTCATCTTGTAGT[G/T]ATGGAATGTTCTGAC | 221178 |
rs186497281 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996019 | ACACAGAGAACTCAG[A/G]TTGCTCATTCCAGAA | 221178 |
rs186498759 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022644 | TTGAAAACTAAAATA[A/C]GAATTTTTTGGGGCT | 221178 |
rs186539953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288173 | TACCACAGCATTCCC[C/T]CTGAGCAGGTCCTGT | 221178 |
rs186549441 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303860 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 221178 |
rs186556315 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978399 | TTGTTTATCTCTAGC[A/G]CCACTTTTTTCTTAA | 221178 |
rs186653977 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24273438 | TTTTGATCTTATTGT[C/T]GTCCACATGTTTAAA | 221178 |
rs186657235 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233801 | GTTCTAGCCAGAGTG[A/C]GGACCCCCTGGGATG | 221178 |
rs186658958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298095 | TTGCACTGTGGCCAC[A/G]TAACATTTAAATCCA | 221178 |
rs186669506 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146181 | TAGGATAGAGGGAGT[A/C]TCAGTCAACAGACTT | 221178 |
rs186692455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184689 | AAGTTCAACGCTCTG[C/T]TAATTTCATGATCTC | 221178 |
rs186693449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108227 | AATCACCGCCTAAAG[C/G]CTCCACCTCTTAATG | 221178 |
rs186698964 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073557 | GGTGACATTGGTGCC[A/G]GTGGCCATAGCAGCT | 221178 |
rs186699441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006748 | AGCTGGGAGAGCACC[A/G]GGACACGCAGCCCAA | 221178 |
rs186704777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089695 | CTACAGGAAGTATTT[A/G]TCATTTATCTGAAAT | 221178 |
rs186705650 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083862 | CTTGTCACTGGGGGA[A/T]AAAACCCCCGTCTGG | 221178 |
rs186716411 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044897 | GAGGAGGGGGTGGGG[G/T]TGGGGGTAGGCAGAG | 221178 |
rs186723681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071208 | GACAGCTGCATCTCA[A/G]TGGAGTCACCTGAGC | 221178 |
rs186740262 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110895 | TTGCACCATCTCTGC[A/G]CATAGCATATTCTTG | 221178 |
rs186742732 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124567 | TGGCAGTCCTGGAGG[C/T]GAATTTAGTCATAGT | 221178 |
rs186748454 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981876 | CTTAAAAACAATAAC[C/T]GTGATGCAATTTTCT | 221178 |
rs186748687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011444 | CCTGGAGAATGTGGC[C/G]ACCCAGCAGCAGGTG | 221178 |
rs186753093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034400 | AACTGGTTGGGTCCA[A/G]TCACTTAATGCAAAA | 221178 |
rs186759251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005628 | GTGGGAGAGGGATGG[G/T]GGAGATCTGAGTTCA | 221178 |
rs186765026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053988 | GAGAGAGCCACAGCT[G/T]CCTCTGTGTCGTTGG | 221178 |
rs186777520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268232 | AAGGTAGATACAATA[C/T]ACAGTGGTTTTCAAA | 221178 |
rs186785311 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124205 | TGATAAACTGATTTT[C/T]GGTTTTTAAAGATTT | 221178 |
rs186795494 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052711 | TCTCAATAAAAGGCA[C/T]ATTTTATAAACAGAA | 221178 |
rs186799213 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089315 | GCATGGGACCCCCCC[A/C]CACACCACTCGGACC | 221178 |
rs186804475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026979 | GTACTCTGTTTCTTT[A/G]TAAGTCAATTTTCTA | 221178 |
rs186809456 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047510 | TTAACAAAGGCAATT[A/G]GCTTGTGAGAATAGA | 221178 |
rs186827900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130094 | GTGGTGGTGAACACA[C/T]AGGCTGATATCATCC | 221178 |
rs186830493 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009347 | ATGAAAAGAATCACA[C/G]TCTGTAAAATATTTG | 221178 |
rs186832150 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987129 | CTACACTGAACCTGT[G/T]AGTAAAATGAGACAT | 221178 |
rs186835692 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24176604 | CTGGGTCCTGGCAGG[A/T]ATCCCAGAAATGACC | 221178 |
rs186838675 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113649 | GGATGAGGCAGGCAG[A/T]TCACGAGGTCAGGAG | 221178 |
rs186843604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093949 | GGCCTCTCCCCGTCC[C/T]GGAGGTTAGATGTCA | 221178 |
rs186849494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170433 | TTGTGGGTGGACACT[A/G]CTCATCTCCTTCAGT | 221178 |
rs186852779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209244 | TTTAAAGGTGCTATC[C/T]CCGTTTCTCTATTAA | 221178 |
rs186858254 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230884 | AAAGTCAGTGACATT[G/T]TCAGGGCAGGGACTC | 221178 |
rs186865435 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978970 | CTGGGATTATAGGCA[C/T]GAGGCACCATGCCAG | 221178 |
rs186868939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192228 | GAGATTCACCAGGGA[A/C]CCCCCTCCCCCCACA | 221178 |
rs186870181 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148597 | AGTGTGATACGTTAG[G/T]AGTTTAATATGGTTG | 221178 |
rs186875818 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038773 | ACCTCTGATCTAATT[C/G]ACAGCTCACTAGGAC | 221178 |
rs186877523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166644 | GCTCCCACCAGACCT[A/G]TAAATTAGTTCTGTG | 221178 |
rs186880829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059770 | CTATGGCGTTTCCTG[A/G]ATAAGATCATGTCGT | 221178 |
rs186885067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127923 | ACTCCTCATGCCTCC[A/G]TTGGCAGAATGATGA | 221178 |
rs186887395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076762 | GAGAGTCACTCTTAT[C/G]TAAAAGGAAGTTACC | 221178 |
rs186938233 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146850 | TTTCTTTACCACCGC[A/T]TCCGTCCCCGCCCCA | 221178 |
rs186939550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163017 | TGTCCCTCAGAAAGC[C/T]TGGGGCCAGTGCCTG | 221178 |
rs186949373 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189404 | GCATGAACCCAGGGG[A/G]CGGAGCTTGCAGTGA | 221178 |
rs186950069 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086922 | AACCAGGAGAAGGCT[G/T]CTGCTTGGCAAACAG | 221178 |
rs186951959 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128670 | GGAAACAGGACTCCC[A/G]GGAGCAAGAGAACCA | 221178 |
rs186958609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092236 | AGATTGTGTTTTAAC[C/T]CAAGTTAGGAAACAA | 221178 |
rs186959919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068982 | ACTCTGTTGATAGTT[C/T]ATTTTTCTGTGCAGA | 221178 |
rs186960984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058841 | TGTCTTCAACCCCAC[A/G]GAAGTTGTCTTTGAA | 221178 |
rs186965576 | snp | C/T | 0.000233953 | 0.010813 | synonymous-codon, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249602 | GCCATTCTCTGACTA[C/T]GGCCAGCTGGCCAGC | 221178 |
rs186968562 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225136 | GTTCCACCCATTCTG[C/T]CCAGCAGGCTGCATT | 221178 |
rs186973945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169546 | CCTTCTCCAGACTCT[G/T]CCCTGGAAATGAGTT | 221178 |
rs186978338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267810 | TGGTCTTCACTAGTT[A/G]GAAAAGATACTGATA | 221178 |
rs186980348 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121754 | AAAAGCTGCCTTCAT[G/T]ACATCCCCTCGTGTT | 221178 |
rs186990479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232808 | CCTGCCTCGGCCTCC[C/T]GGAGTGCTGAGATTA | 221178 |
rs186998531 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173179 | GCCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCTC | 221178 |
rs187000936 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106591 | TACAGAACAGCACTC[A/G]CTTTGTGTCTCACTG | 221178 |
rs187005502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287443 | GCTGGGATTAGAGGC[A/G]TGAGCCAGTGTGCCC | 221178 |
rs187017410 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070929 | TCCAGGCTGCCAACT[C/T]GTGCTGCAGATCTTA | 221178 |
rs187018708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204352 | CAAATATATTTTGGA[A/C]ATGCTTAATTTAACT | 221178 |
rs187021792 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245160 | AGTCTGAGTTAGGCT[C/G]TCACTTGTTTGAGAA | 221178 |
rs187031100 | snp | A/G | 1.74455e-05 | 0.00295338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24270930 | ATGTGTGCAAAGAAT[A/G]GATTGTTGTACTGTG | 221178 |
rs187034929 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264420 | GGCCTTAGAAATATT[C/T]GGTAACTTTTCCTAG | 221178 |
rs187062547 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001135 | CTTCTACTCTCACCC[C/G]CTACTCTCTCCAGGT | 221178 |
rs187063403 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133706 | TATTAGCAGACAGCT[A/G]TGGGGGAAGCTGGCC | 221178 |
rs187071515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174219 | AAAGCGGTCCATTTT[A/G]TTGAAGTTGTCAAGT | 221178 |
rs187075944 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154307 | CCATCAACAATAGAA[C/T]AGGACATAGTATATT | 221178 |
rs187082646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206184 | TATCCATCTGACAAA[C/G]GTCTAACATCCAACA | 221178 |
rs187089996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227832 | ACCTCAGCCTTCCAA[A/C]GTGCTAGGATTATAG | 221178 |
rs187091529 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190076 | ATATACTATATATAT[C/T]ATTATATAACATATA | 221178 |
rs187131299 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202918 | AAGCAAACAGGAAAA[C/T]CCTAACTTAGGAAAC | 221178 |
rs187135857 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142144 | TTTATGCTACAAATA[A/G]GACAGAGGGGTCTTA | 221178 |
rs187136229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172361 | GAGTTTTTCATTTTG[A/G]TGAGGTCCAGTTTAT | 221178 |
rs187144304 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305758 | CTATTCCATTCTTCA[C/T]GTTTCAGAATTGGTC | 221178 |
rs187169262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241203 | CCAGAGTTATTATTT[A/G]TTTTTACCTACAAGC | 221178 |
rs187193705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213389 | CTTTTGCCTCAGCCT[C/T]ACGAGTAGCTGGGAC | 221178 |
rs187199527 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189966 | TATTATATAATTATA[A/T]AATATATATTATATA | 221178 |
rs187207197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153548 | ATCAGTGAAGGCAGC[C/G]AAGGCCACTTTCAAC | 221178 |
rs187216584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252012 | CTCATCTCAGGAGAA[C/T]GGTGCATCATTTGCT | 221178 |
rs187223915 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290259 | AGACTAGTTGTAAAC[C/T]ACAAAGAATAAGCAA | 221178 |
rs187231532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226692 | CTTCCCACCCATCCC[C/T]GGGGAGGACCTCAGT | 221178 |
rs187264255 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986608 | CTCCATTTTTACACA[C/G]AAGGTTGGGAAAGTC | 221178 |
rs187276676 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24209130 | GATAGACATCATGAG[A/C]CTCTGGCTTAGGTGC | 221178 |
rs187287502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008320 | TTTCAGTTTTCCTTC[A/G]TCTCAGAGAAAGAGA | 221178 |
rs187300499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248635 | CCTCGTTCAGTGCTC[A/G]CCCCATCAGACTGCT | 221178 |
rs187304566 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286539 | GAAATTAGGCTGGGT[C/T]GGAGCAAAAATGTTA | 221178 |
rs187310395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059347 | CAAAAAAAAAAGGCT[C/T]GTCTTTGATCTCTCA | 221178 |
rs187316305 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075876 | TTTATTGATGTCTCT[C/G]TCCTGGGAGAAGAGA | 221178 |
rs187317239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031667 | GGCACTGTAGATGCA[A/G]AAATAGCTAAGACCT | 221178 |
rs187324003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998234 | TTTACATTCTCAACA[A/G]CACTTGGAATCATCA | 221178 |
rs187326639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070873 | GGATCTCAGAACTGC[C/T]GGCCTTCAGACTGGA | 221178 |
rs187332944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990374 | GGCATGCCCTGGCTC[A/G]CTCCCTCTGTTTCCT | 221178 |
rs187342580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015936 | GAGCATCAAAGACAC[A/G]CTTCTGTCCTTCGTC | 221178 |
rs187343892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038103 | TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 221178 |
rs187392977 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063993 | ACCGCCTCCAGTGGG[A/T]GCCTCTGGAGCAAAC | 221178 |
rs187396306 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082258 | ACTCTCTCATAAGCA[C/T]GTAAGTGTTCTGTGG | 221178 |
rs187396544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275631 | CTTGTTTACAAGATC[A/G]TTTCCAAAAATGGCT | 221178 |
rs187401728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254736 | TATCATCAGCTTTGT[C/T]GAGGGGAAGGCCCAG | 221178 |
rs187408700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292550 | TCCTAATGAGAAGAG[A/G]AAGAGGGAAGGGATT | 221178 |
rs187460283 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230588 | TTGCTAAACCTCATT[G/T]TCCTTGCCTGTAAAC | 221178 |
rs187497901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134107 | AAGGTAGAATGGTAC[C/T]CAGATAGAACTCTGC | 221178 |
rs187501570 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267518 | ATCCTCTTGTACCGG[A/C]TGCCGATGAAAAGTG | 221178 |
rs187507911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296132 | TTTAACTGAAATAGG[C/G]TATAGGTGGTGAAAA | 221178 |
rs187511729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116612 | ATTTTACAGATGAAA[C/T]GTCTCAGAGGGTAAT | 221178 |
rs187518292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097419 | GACCAGAAAACAAAA[C/T]TGGCAGAAAAGAGCT | 221178 |
rs187522779 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173867 | ATATGTATTGCTGAA[G/T]TCTGTTTTGTTAAGC | 221178 |
rs187530601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154074 | GAAGGTGGGGGACCA[C/T]GTAGAACTCTCTTCT | 221178 |
rs187541901 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116824 | TTTGGGAGGTAATTA[A/C/G]GTTTAGATGAGATCA | 221178 |
rs187544667 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142661 | TCCTCCCCCTTTCCT[A/C]TTCCTCATCCTTCTT | 221178 |
rs187547892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043019 | TGTGTCTTAGTGAAT[A/G]ATGCCAGTATTGGCT | 221178 |
rs187578253 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991259 | TTTTCTTTGTAATAC[A/C/G]TTCGTGTCCCTCTCT | 221178 |
rs187587467 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24051643 | CTGTTTGGGGATGGA[A/G]GGGTGGGGACTTAGG | 221178 |
rs187594636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059184 | CACCGTGTTAGCCAG[A/G]ATGGTCTCGATCTCC | 221178 |
rs187608219 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197966 | TCCAACTCCTCACTT[C/T]CCCATGTTTCCTCCC | 221178 |
rs187614307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010706 | CTCCCATGAATCTTC[C/T]TCCCCACTCCTCCCT | 221178 |
rs187620320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092876 | GTAACAACTAGAAGA[C/T]TGCCCGAGTAAGCCT | 221178 |
rs187623046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234701 | GACTTCAGGGAGTCA[A/G]CTGGTGCAGGAATAG | 221178 |
rs187623680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014839 | TTCCACAGGATTGCT[A/G]TAGTTCTGAGATCCA | 221178 |
rs187626179 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041943 | TGACACACAGTCCTC[A/G]CCTTTTCCTCATGCT | 221178 |
rs187633885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063478 | CATCCTCTCCCCTGG[C/T]CCACATCCCTCGGTG | 221178 |
rs187638946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216168 | GCAGGGAGGGGCATT[A/G]TGGAGGATGCCAGCA | 221178 |
rs187641481 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080969 | GTTCCCAATGCTCCC[C/T]TTTGTCATTCCGAGG | 221178 |
rs187651493 | snp | G/T | 2.26109e-05 | 0.00336228 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300510 | TTGTCCCCTTAATGC[G/T]TATCAGTATTCTCCT | 221178 |
rs187658234 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285147 | TGGGCGCTAAGGAGA[C/T]GGGCAAAATCACCTG | 221178 |
rs187699200 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193041 | GTGTGTGGGCTGAGA[G/T]CCCTGGGGGGCCAGG | 221178 |
rs187700490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143933 | AAGAACACCTATCTC[A/T]TGTGGTTGCCCTGAA | 221178 |
rs187700665 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125180 | CTTGCGTGGAGAGGC[C/T]GCTACACTGGCTCTG | 221178 |
rs187711515 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108399 | CCTAGTGGGACGTGT[A/G]CCTGTTTATATTTTA | 221178 |
rs187717805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231155 | CACCTTTTATTAAGC[A/G]AACAATTCAGTGATT | 221178 |
rs187731759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163943 | TTTTTTGTCTGAAAA[C/T]TAAACATTTAAGAAA | 221178 |
rs187732009 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182858 | TGCGCCACATCAGTC[C/G]GGCCAGGTAAACAAA | 221178 |
rs187742778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280208 | TGTTTATGAAGAACT[C/T]AGAGAGCAGTCAGTA | 221178 |
rs187750366 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265158 | CCTGAGCTGTGTATG[A/T]TGGGGCCCGCCCCTC | 221178 |
rs187757987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158487 | GCGTCGGCTGGTGAT[A/G]TACTCCCGTGATGAA | 221178 |
rs187795765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020548 | ACGAATTGTATTTAA[A/C]CTTTAACAGTCCATC | 221178 |
rs187804598 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098581 | CTGCCTAGGAGATAG[A/G]GTGAGACTGTCTTAA | 221178 |
rs187805435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138300 | GACAGAGCAAGACTC[C/T]GTCTGAAAAAAAAAA | 221178 |
rs187858602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215745 | TAGCCTGTGAACTCA[C/G]TGAACACAGCTCCAG | 221178 |
rs187859970 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026767 | TATTTTTAGTGGAGA[C/T]GGGTTTTCACCGTGT | 221178 |
rs187865326 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991996 | GCACTGCCATTGTTG[A/T]GTGGTTACTACAAGC | 221178 |
rs187865727 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002553 | CCTGAGGCCTGGTCA[A/C/G]GGGGGTGAGTGTGTT | 221178 |
rs187867856 | snp | A/T | 0.039522 | 0.134904 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019099 | ATTATTATTATTTTT[A/T]TTTTTTTGAGACGGA | 221178 |
rs187868716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234120 | AGAGACTAAATGCCA[A/C]CTCTTATAGAAATTA | 221178 |
rs187877303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075064 | GGTTAGAATATGTGA[A/G]GAGGCACCTTTAGGC | 221178 |
rs187878680 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067943 | TCCTGACCTCAGGTG[A/T]TCTGCATGCCTTGGC | 221178 |
rs187896033 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997335 | AACACGCATGTCCCC[A/T]GTGATCCGACCGTCC | 221178 |
rs187898236 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278570 | AGCATGAGCTACCAC[A/G]CCCAGCCACATCTTG | 221178 |
rs187898802 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980558 | GGTGTTATGGAAGAC[A/G]TGAACAAGAATAGTA | 221178 |
rs187904286 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038068 | AGGCGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 221178 |
rs187906488 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258960 | GAGAGCATATCCTAG[C/G]TAGCCACTGGGGAGC | 221178 |
rs187909944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210997 | TATTTTATTCTTTTC[G/T]ATGCTTTTGCAAATT | 221178 |
rs187910094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295566 | GCAGTGAGCCGTGAT[C/T]GTGCCCCTGCACTCT | 221178 |
rs187941666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238523 | TCTGCTAAGGTGCTT[C/T]AGTCCCTTTTCTGGC | 221178 |
rs187945890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200985 | AATGTTGCAGCTATT[C/T]TAAGGGCTTTGCACG | 221178 |
rs187947723 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159619 | ATTACTTACAGGAGG[C/T]TCACGCCGCATGCTG | 221178 |
rs187974217 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210487 | TGCATGTGGATATTC[A/G]GTTTTCCCAGTACCA | 221178 |
rs187974374 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278992 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 221178 |
rs187975026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237950 | TTAAATATGCAATAT[A/G]TAAACATACATGTTT | 221178 |
rs187982128 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24177389 | CAGCAAATTCACTGT[C/T]GGCGTGAATGCCTGC | 221178 |
rs187990713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178192 | ATCTGCACCAGATCA[A/G]CATAAAAATTTCCAG | 221178 |
rs188003432 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261166 | ATCATTGGCTGGATC[A/G]TGGAGGACTGGAGAC | 221178 |
rs188015893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250635 | GTACTAGTACTGGAT[A/T]GTATACGTCTACATT | 221178 |
rs188018821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240338 | CGTGTTACTATTGAT[C/T]TTGAGATGGCAGGAT | 221178 |
rs188039724 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112303 | AAAATCTACCCTTAA[C/T]TCACTGGGTCAGTTT | 221178 |
rs188042817 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24214443 | TTTGATGAGAATTTT[C/G]TCTTTACAATGCATG | 221178 |
rs188043125 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182359 | GAGGTTAAATTGGCT[C/T]ACGGTTCTGCAGGCT | 221178 |
rs188057449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036728 | TCTCACCTTACTAAA[C/T]AACAATTATCTCTTA | 221178 |
rs188058436 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138840 | CAAGTAATCCTCCTG[C/T]CTTGGCCTCCCAAAG | 221178 |
rs188061415 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057739 | GATCTTTTCTCTGGT[C/G]TCTGAGCACCTTGAC | 221178 |
rs188072175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157815 | ACTGCTTTGTTCAGA[A/G]CATTTTCAAACAGGA | 221178 |
rs188072607 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072490 | TCCTGTTCTATCAGG[A/G]CTTCTGATGCACCTA | 221178 |
rs188095939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187348 | TGAGTAGTCCTAGCT[A/G]TCTTCAGTTCTCAGT | 221178 |
rs188099319 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305189 | AAGAAATGGTTTGCA[C/T]TTTGTGGCCAGTCCT | 221178 |
rs188139893 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120866 | AGGGAAAAGTACACT[G/T]AGTTCTATTCACAAA | 221178 |
rs188148433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046939 | GGCTAGCCAAGCAGA[A/G]CAGGAGTTTATTACT | 221178 |
rs188159194 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086142 | TGAGTTTGACTTTCC[C/T]TATGAAGGCAAGACA | 221178 |
rs188176470 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290207 | GAATTGGGAAGAGAG[C/G]TATGTTGAAATGGGC | 221178 |
rs188213179 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24222099 | ATTACAGGCGTGAGC[C/G]ACTGCACCCAACCCT | 221178 |
rs188231813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299461 | TGTGGGTAGAAGCTT[C/T]AGGTAGCAGATCAGA | 221178 |
rs188242377 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063354 | GGTTTTGAAATTTGT[A/G]CACATTGTGGGATGG | 221178 |
rs188243490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260407 | ACAGTGTGGCCTGCG[C/T]TTGCCTTCCTGGCTC | 221178 |
rs188251715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171171 | CAGCCGCTGACTGCT[C/T]ACTAGAGCTGGGTGG | 221178 |
rs188255916 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295763 | GTCTGAATGGCACTG[A/G/T]TCTGAGCCATTTGTA | 221178 |
rs188263134 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123295 | CAATCAGACATCTTC[C/T]TGTCAGCTCTAAGGC | 221178 |
rs188267281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106272 | CTCCTGGCCTCAGTG[A/G]TCTTTCTGCCTTGGC | 221178 |
rs188267566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150056 | GGTATCTGCCTGACT[G/T]GTGGCCAGGTGTGCA | 221178 |
rs188285137 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223390 | CAAATGGCGCTGTCC[C/G]AGGAGCCCAGGCAAG | 221178 |
rs188290898 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300116 | GTGGGAATATTTGCC[A/C/T]GGGAGCGTCGGGCTT | 221178 |
rs188293651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188126 | CGGGCAGATTGCCTG[A/G]GCTCAGGAGTTCGAG | 221178 |
rs188296670 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977905 | CTTTTCTTTTTTATT[A/T]ATTTATTTATTTTTT | 221178 |
rs188298292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141445 | TTTTCCTGCTTCCCT[C/T]CCACCTGCTGTGCCT | 221178 |
rs188300531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202049 | CATTTCTCCAGCCTG[A/G]GGGACAGAGCAAGAC | 221178 |
rs188310318 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050154 | GGATTACAAGTGTGA[A/G]CCACCATGCCAGGCC | 221178 |
rs188316216 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070731 | TCCAATCAGTTAAAG[G/T]CCTCAATAGAACGGA | 221178 |
rs188317521 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196774 | AGCAGCCTAGTACAT[A/G]TCGGGCACTTAGTGT | 221178 |
rs188318018 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113338 | CCAGGTGCAGTGGCT[C/T]ACGCTTGTAATCCCA | 221178 |
rs188326221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088944 | GGGAATGATCTGGGT[C/T]TGGAGACAGGGATGC | 221178 |
rs188335916 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046132 | TATGCAGAAAAGCGT[C/T]TAAGTCAAGTGTGTA | 221178 |
rs188343615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302179 | ACCCTCCTTGGAGGC[C/T]TTTTGGGAGAGTTCA | 221178 |
rs188345832 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030528 | TCCCTAATCTCCTGC[C/G]CACCCATGTTTCCAT | 221178 |
rs188369972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007922 | GCACATGCCACCCCA[A/G]GAAAGGACAGAAATT | 221178 |
rs188375421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049839 | CAGGAAGAGGGAAAT[A/C]GGATTCTTTCCATTT | 221178 |
rs188405801 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988068 | CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGATTA | 221178 |
rs188409904 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009820 | CTTTTTTTGAATTCC[A/T]AAAAGGAGGAGGGTA | 221178 |
rs188412439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981362 | TACAAATTATGTTAT[C/T]TGTTTACTCAGATAC | 221178 |
rs188413671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028385 | CATCATTCTTGAAAC[A/G]GTTTTGCTGGGTACA | 221178 |
rs188424301 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019330 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 221178 |
rs188483349 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227342 | ATATATATGAACTAG[C/T]GTGTAGTTATTTGCC | 221178 |
rs188501763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164328 | GAGCCCCCTTGCTCC[C/T]GCCTCTGCTCCCTCC | 221178 |
rs188503816 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263582 | CCTCCATATACTTTA[A/T]ATCACCTCTAGATTA | 221178 |
rs188559602 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125645 | TCTTCCTTGACTTAG[C/G]TGAGATTGTCAAGAT | 221178 |
rs188559620 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190023 | ATTATTATATAACAT[A/G]ATGATATACAATATA | 221178 |
rs188562585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093495 | CTATTAAATGGTCCC[A/G]ATACAGATGCAAAGT | 221178 |
rs188582710 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269841 | TGATCCTCCCACCTT[C/G]GCCTCCCAAAGTGTT | 221178 |
rs188596963 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304996 | AATAACTGTAGGGGT[C/T]TCTGCTAGAGTTGTT | 221178 |
rs188597102 | snp | A/G | 9.91359e-05 | 0.00703975 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24289022 | CCGACAGTGCCGCAA[A/G]CACACAGGAATGTTC | 221178 |
rs188597445 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126944 | ATAATGGGAAGACTG[A/G]AGATTGTGAAATCAA | 221178 |
rs188598297 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129221 | GTTTCCACAGTCCAC[A/G]CTGAATGCTGGGGGT | 221178 |
rs188607842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110284 | TTGGTCAAGGAGTGA[A/G]GAAGGGAGGGGAGGA | 221178 |
rs188617986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090987 | TTCTATAAAGTCTGC[A/C]TTTTTTGTCATTTGT | 221178 |
rs188629684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152616 | CCGTCTGTGTGACCA[C/G]TGCTTTCAATCACAG | 221178 |
rs188635014 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071569 | GGGAAAACCAGCACG[C/G]AGAGATGTGACCTCT | 221178 |
rs188639765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144792 | TCTGGTGGCAGCCTC[A/G]TGCAGTACGGTATGC | 221178 |
rs188640401 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193387 | TGACACAGGCGGTGG[C/G]CATGTTGTTTGTACT | 221178 |
rs188646528 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132760 | AGGTGGATCACCTGA[A/G]GTCAAGAGTTCGAGA | 221178 |
rs188647331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986119 | AGTTCTGGTGTGTTA[A/G]GTTTGCAAGTGTTTT | 221178 |
rs188653021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231958 | CATTGCATTCTTTGT[C/T]ATCCTTTTATTGAGC | 221178 |
rs188656326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026117 | CTTGGCTACTACTTT[A/G]TTGGTTACATTGGTT | 221178 |
rs188664359 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042842 | TGTGGTCTGAGAATC[A/C/G]CATGTTGAGAAACAC | 221178 |
rs188665584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251317 | GGCCACCCTGGCCGG[A/G]TTTGTGGCCTTGTCC | 221178 |
rs188667284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172430 | TCTAAGAACTCCGTC[A/G]TAGTCCTAGATCCTG | 221178 |
rs188667456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211147 | TGTTTATTAGTTCTA[A/G]CAGTTTTATGGTAGT | 221178 |
rs188669617 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035581 | CAGCCTAACTCAGAA[G/T]AAAATAAGAAACAAA | 221178 |
rs188672310 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189698 | TATATATAATATATA[A/T]TATATTATATATAAA | 221178 |
rs188675824 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097075 | GGCCCCGGCTGAAAC[C/G]GTGCCAGTGGAGTTG | 221178 |
rs188690582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003862 | GACGTGGGAAAAAAC[A/G]CAATATACATCAGCA | 221178 |
rs188698545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175044 | TTTCAATTCTTTTAA[A/G]TTTGTTGAGGTTTGT | 221178 |
rs188714874 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207365 | ATCCCGCACATGTAC[A/C]CCTGAACTTAAAATA | 221178 |
rs188718917 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246993 | CTTTCAGGAAAATAC[A/G]TGAGTTTTGTGACAG | 221178 |
rs188725343 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229823 | CCAGTTAGGTATGAC[C/T]CTATAGGGAATGTGG | 221178 |
rs188728372 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206482 | GTATAAATTAGTTCA[A/G]CCCTTGTGGAAAACA | 221178 |
rs188744960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294172 | AACATTTTAGCTTGA[C/T]GTGACTGTGGTGGAC | 221178 |
rs188753130 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245507 | TAGAATATGTGGTAC[C/T]TTTTAGAGGGAATGT | 221178 |
rs188756749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274177 | ATCAGAATCCATTGC[C/T]TGCAACTTGTGGCTT | 221178 |
rs188763122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183255 | ATGAAACATTTTTCA[A/G]TACAAGTCAAATATA | 221178 |
rs188794461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251076 | GGCCTTTGATTAATA[G/T]TTTTAGGGATCGCTA | 221178 |
rs188795141 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244851 | CAGAGTGAGACTGTC[A/G]CAAAATAAATAAATA | 221178 |
rs188805161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288532 | ACAGATTGATGCTGT[A/C]CATAGAAAGGCGGTG | 221178 |
rs188805357 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284492 | ATAGTGAAACCCTGT[A/C]TCTACTAAAAATACA | 221178 |
rs188828050 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186634 | TTAGTTCCCTTTCAG[A/G]GTTTCTTAACCTTCA | 221178 |
rs188829177 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277264 | CCTGGCTAACATGGT[A/G]AAACCACGTCTCTAC | 221178 |
rs188830510 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266011 | ATCAGAAATGTGGAG[C/G]TCAAAGGAACCTTAA | 221178 |
rs188834960 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236185 | GCCTCCTCATCTCTT[A/G]AGGAATCACTTAATC | 221178 |
rs188835736 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144084 | TGTTCATGAGCTGAA[G/T]GTGCACTAACTCAGT | 221178 |
rs188836845 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301530 | GTCCATATCTTCTGC[A/G]AGTCACTCGCCCAGC | 221178 |
rs188839092 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257599 | TGCTCAATTTGATTT[G/T]TTAAATTTTTACTTT | 221178 |
rs188844542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148310 | CAGTCCTACTTTCAT[A/G]AGCCCCGTTGTCTTT | 221178 |
rs188846601 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285985 | CACGCCCAGTTTAAG[C/T]GCTTTCTTTAAAAGC | 221178 |
rs188853964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109473 | TTTGGGTATATACCC[A/G]GTAATGAGATTGCTT | 221178 |
rs188892332 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992710 | GAAAGGGGCCCTGCA[A/G]GAGAGGGATCCTGCA | 221178 |
rs188939638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089876 | AGGGCCCAGTCTCCA[C/T]TTCCAAGATGATGTC | 221178 |
rs188941954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011952 | CCTCCGCCTCCCCCT[A/G]CGGATTGTAAAACTC | 221178 |
rs188943935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115925 | CTGTCCTTACAACCT[A/G]GTAGCTGGCTTCTCC | 221178 |
rs188944825 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24012554 | GCCCTTCGAGTTGGC[C/G]ATGTTGATCAAGTTC | 221178 |
rs188952311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054887 | TCATACAATAACAGC[A/G]CTCACTTCTTGTGAT | 221178 |
rs188960379 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036276 | GCAAATCTCCCTGGC[A/G/T]TCAGGGTTAATGGAA | 221178 |
rs188975403 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017277 | TCCTCATCCGAGAAA[C/T]AGAATAATTTGCCTG | 221178 |
rs188982420 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040597 | CCCGGGGAGACACAG[A/G]GGTCCAGGACACAAA | 221178 |
rs188993120 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062100 | ATGACCCACCCATGG[A/G]GGTATCTTGAGGAAC | 221178 |
rs188999233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104618 | GTGACAATGAGAGGG[A/G]CATGTGGAATGCAAA | 221178 |
rs189004647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978604 | TCTGTCTTTTGGTTC[A/G]ACTGTTTCATCTATT | 221178 |
rs189020812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000584 | TTTGCTAATGTGATC[A/C]AGTCTATGAAGTGGT | 221178 |
rs189021486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253666 | GATGACTTTGGGTAA[C/T]GTGAGGAGTAGGAGC | 221178 |
rs189040275 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24194108 | GATCTTTGCTGCTTT[A/G]TGGTTTTATGAACTC | 221178 |
rs189045680 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228274 | ACCTGCCACCATGCC[C/T]GGCTCATGTTTTCTA | 221178 |
rs189050791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270243 | ACAACCCAGAATATA[C/T]TACCTGGAGAGAACT | 221178 |
rs189076340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231503 | TTGTTATCTGTTCAT[C/T]TGTTGATGGAGATGG | 221178 |
rs189092130 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268806 | TTTCAGCTGAACTGG[G/T]CATAAGAGTTTGTGT | 221178 |
rs189094005 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304843 | TCCTGTGGCATGTGT[C/G]GGGGTGTGTGTGTGT | 221178 |
rs189112917 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013250 | CTCCTCAGCTCAGCT[C/T]CCGCTCTGTAAGTGG | 221178 |
rs189115380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056813 | ATTTCCAAGCTGATC[A/G]GGCCACAGGTCCAAT | 221178 |
rs189127951 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169822 | CAGTGAGTCCCCACT[C/G]TCCTCTCCTGCCTGG | 221178 |
rs189144865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200498 | TTGAATGTCCCACCT[C/T]GTTCTCAGCCCCAAG | 221178 |
rs189161965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127474 | GCCCCCGTAGGTAGT[C/T]TACTGAGAACAGCCT | 221178 |
rs189171022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155953 | TGTCCTTTTGTGATG[A/G]GCTTATGCATTTAAT | 221178 |
rs189176999 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135486 | GCAGATCACGAGGTC[A/G]GGAGATCAAGACCAT | 221178 |
rs189189287 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118125 | AATATTATGAGGAAA[C/T]CTGGAACAGCACGTA | 221178 |
rs189194466 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016615 | TCCAGGGCCCGGGCA[G/T]GGCCTGCAGGGCTGT | 221178 |
rs189200095 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190142 | ATATACAATATATAT[C/T]ATTATATAACATATA | 221178 |
rs189206130 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207282 | TGCTGGGCTTAATAC[C/T]GAGGTGATAGGATGA | 221178 |
rs189207697 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174703 | TGCCTCAGTCTCCCA[A/G]GTAGCTGGGACTACA | 221178 |
rs189230383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256773 | CATGTTTGTAGGCTA[C/T]TGGGTGTGTTATTTG | 221178 |
rs189231249 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083760 | GTTTGAAACACACTG[C/T]GCTCAGCCACATGGA | 221178 |
rs189241017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235486 | ATTGGTCTGGCTGAC[A/G]TGGTGGCTCATGCCT | 221178 |
rs189247542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100229 | TATGGTCTTTCAATG[G/T]GTTTACTGAACCTTT | 221178 |
rs189277155 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166502 | TCCAGCTTGGTGACT[C/T]GAGGGACCCTTGAAC | 221178 |
rs189278487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098787 | CAAAAATTAGCTGGG[C/T]ATTTTGGTGCGTGCA | 221178 |
rs189283094 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184377 | ACAGAACCTGCACCT[A/G]CTGTGCGGGTCCCAG | 221178 |
rs189287518 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145766 | ATTTTCAAATTGGTG[A/T]TGCTGCTAGGAGGGC | 221178 |
rs189292425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131375 | CCAGCTGACTTCTCA[C/T]AGGGCTGACTCACAA | 221178 |
rs189301762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083186 | CAGTAACTTGGGAGC[C/T]GAGTAAGTTCTCTAT | 221178 |
rs189303043 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218592 | CTTTCAGTGTCACTT[C/T]GTTATCATGTAAATC | 221178 |
rs189314157 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161741 | GTGGGTCATTTGCTT[C/G]CCAGCATTGCATAGG | 221178 |
rs189321006 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021557 | GTTGGGCTGCATTGT[A/C]CTCAAACATAAATGC | 221178 |
rs189323535 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198273 | GCTGAGATTACAGGC[A/G]TGAGCCACCGCACCG | 221178 |
rs189330834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211510 | ATCTGTTGAGATAGT[C/T]CTATGATTTTTAGCC | 221178 |
rs189331495 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043762 | AGGTCACATTCTGCA[C/G]CATGTTTTCCCGATT | 221178 |
rs189340279 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064591 | AAGACAGACATCTAC[A/C]AACCAGGAAGTAGGC | 221178 |
rs189343290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251593 | AGCCTGCAACTCGTG[A/G]CAGGATTGGAGAAAC | 221178 |
rs189361997 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23982680 | AATGCATTATCTTCA[C/T]TGAGCCTTACAACAA | 221178 |
rs189363504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094692 | TGAGCCCAGGAGTTT[A/G]AGGTTACAGTAAACT | 221178 |
rs189364599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005911 | CCTTGACCTTTAGAG[A/C]TGATCTTCTAAAAGA | 221178 |
rs189365519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061141 | TCAATATCACTAATA[C/T]TAGAGAAATGCAAAT | 221178 |
rs189368227 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240825 | TCTTTTATCATCCAC[A/G]TAACACATTCAAGGA | 221178 |
rs189369984 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24261539 | ATATGAGTGGGGGTA[A/G]AAATGAGAAGAGGAT | 221178 |
rs189383248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993925 | GCCAGCTGGGGTGAG[C/T]GATGATTCCCTGAAG | 221178 |
rs189397984 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140923 | GCTCACGCCTGTAAC[A/G]CCAGCACTTTGGGAT | 221178 |
rs189405903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070091 | TAGTTTAGCTTGGAC[A/G]GTGTTTCACATACTG | 221178 |
rs189420195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105339 | AGACGGGGATCTGCC[A/G]TGTTGTCCAGGCTGG | 221178 |
rs189454868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999141 | CATGTTGGCCAGGCT[A/G]GTCTCGAACTCCTGA | 221178 |
rs189472271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999528 | AACAGCAGGTGATAG[C/T]TTTAAGTGTACAGAC | 221178 |
rs189475960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296728 | TCCATTAATTCAGCA[C/T]GCCTCTTACCAGAGG | 221178 |
rs189481899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281638 | GGCTGGGATGTCGGG[A/G]TTTCTCTGAGAGGGG | 221178 |
rs189504063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281844 | CGCCGCTGGCAGCAC[A/G]TGCACACCTTCCTGC | 221178 |
rs189525156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179254 | TGTGTACAAGTTTTT[A/G]TGTGGACATCTGTTT | 221178 |
rs189526639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095392 | ATAGGAAATAGAAGG[C/G]TGGTTACCCAGGGCT | 221178 |
rs189530174 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122248 | ATGGTGAGTCAGAGC[C/G]TGATACCACACAGGA | 221178 |
rs189543655 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24079420 | ATGGATTGCAGAGAA[C/G]TCAGAGATGGAGCAG | 221178 |
rs189554463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203054 | CGTGTGCCATGGTGG[A/T]TGGCTGCAGATCATC | 221178 |
rs189566016 | snp | G/T | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307395 | CTGTGCCCTCTGACT[G/T]CCCCTGAAGGCTAGG | 221178 |
rs189573494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217123 | TGGTTTTAACTGGCC[A/G]TGGTATGTACCTGTT | 221178 |
rs189582563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180170 | TGTGCTCTATTTTGC[A/G]TATGGTGTAAGGGAA | 221178 |
rs189591978 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156382 | GGGGGCCCTGTCTCC[A/C/G]AGCAGACAGGGAGGC | 221178 |
rs189603353 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255738 | CTCTAGCATTTCCAT[A/C/T]CCAGTCCTGGAACTC | 221178 |
rs189614497 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293533 | CATTTGCAGATTTTG[G/T]TTTTTTCAAAATAAA | 221178 |
rs189629528 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007012 | TCCGTGTGGAGCCCC[C/T]TTTCCTCTAGGATGC | 221178 |
rs189634007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022988 | GTACATGTGCACAGC[A/G]TGCAAGCTCGTTACA | 221178 |
rs189639513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083888 | TCTGGAGATGCAGGT[A/G]CTCTTCTGACATTTT | 221178 |
rs189640747 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114358 | AATTCAGTGTGCACG[A/T]GTGTGCCTGCATGTG | 221178 |
rs189642259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039827 | TCAATGCTGTCATAA[C/T]GATACCACATTTGCT | 221178 |
rs189651256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283643 | GTTCCAAGCCTTTCA[A/G]ATATGTACAGAGAGT | 221178 |
rs189654435 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077576 | CCACCAGTACACAAG[A/G]TACCCCGTAACAAAC | 221178 |
rs189657614 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985359 | AGGTTGTGTCATGGC[A/G]TGGCCACCCCAGGAA | 221178 |
rs189659512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262408 | ATCAGATCACACCAC[A/G]TTTCTGTTTTTTCTT | 221178 |
rs189661247 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088249 | AGTGTTTGAGGTAGG[A/G]ATTGTTTGCATTCTA | 221178 |
rs189669215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184081 | AAGTGTGGAGGAGAG[C/T]GCCAAGGGACAGTAA | 221178 |
rs189675296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118843 | CCACACGCTGGTTCC[C/T]GTGTTCAGTAAGAAC | 221178 |
rs189692936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122803 | TCTGTGGAGACTCTC[A/G]TTGTCATGTCAAACT | 221178 |
rs189702208 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189764 | CATATATAATATATA[A/T]TATATTATAAATATA | 221178 |
rs189705406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163457 | CAGCTGTCTCCTCCC[A/G]TGCATTGAGAGTTCC | 221178 |
rs189709482 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143419 | GCATTAGAATAGAGG[G/T]TTTGTGTTGATAAAA | 221178 |
rs189720107 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188343 | TCTCCAAAAAAAATA[A/T]TAAAAAAAAAAAGTG | 221178 |
rs189723501 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124973 | GAAAGGAACTGAAAC[C/T]CATTCATAGGGTCAG | 221178 |
rs189723672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173001 | TGTACGGCTTTCAGC[A/G]CACAGGTTTCATACA | 221178 |
rs189731208 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24241899 | CTCTACAGAAAATTT[A/T]AAAATTAGCTGGACC | 221178 |
rs189738622 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203844 | AATGTTTACAAAGAA[A/G]CTCTGAATGTTTCAA | 221178 |
rs189744287 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016462 | GGAAGAATTGGGAGC[A/G]TCCTTTGGTGCCTGG | 221178 |
rs189744544 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226371 | CCTGTCGGCCTTTGA[A/C]TGATGCTTGTTTAAA | 221178 |
rs189761042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261935 | TACCCCATAAAGGCT[C/T]AGGACTAATGAAAAA | 221178 |
rs189762948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225937 | AAAATGAAGTTACGT[G/T]GACAAACGGAGGGTG | 221178 |
rs189791456 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297950 | GCAACATTTATTCAG[C/T]ATTTACCTTGTGCCA | 221178 |
rs189817953 | snp | G/T | | | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160445 | GACGGGGTTTCACCA[G/T]GTTGGCCAAGCTGCT | 221178 |
rs189845121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198728 | AAGTCTGGGTCGTCC[C/T]GTGAGGGCTATCCCA | 221178 |
rs189853417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235062 | TAAATCGGGTTAATA[C/G]TAGCTTTTATAACAG | 221178 |
rs189856209 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265370 | ACTGTGACCTGTAGA[G/T]TAATAATCATGTTTG | 221178 |
rs189857467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198207 | ACTGTGTTGGCCAGG[A/C]TGGTCTTGAACTCCT | 221178 |
rs189861978 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229308 | ACCCCTCTCCAGGGA[C/G]CTATGGTAAGCTGCA | 221178 |
rs189863812 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002078 | GGGAGTGACGAGAGG[G/T]CACTGTGCAGTGGCA | 221178 |
rs189878177 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019041 | TCAGGGAAAGTGAAC[A/G]TGTCTAAAGAAGGGG | 221178 |
rs189890190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300968 | AGACAAAAAAAGACA[C/T]GTGAGCTGATTTAGG | 221178 |
rs189891008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276540 | TTAATATGTGTGGCC[A/G]TTCTGCAAGATGAAA | 221178 |
rs189902080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278386 | ATCTCCACAGCTTAA[A/G]TCAGTGCCTAGCACA | 221178 |
rs189902376 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979655 | ACTGCTCATCGCCAG[G/T]GAAACGCGGCATTCG | 221178 |
rs189915560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009523 | GTAAAGATGTACATT[G/T]GTTTGGTCTGGAAAG | 221178 |
rs189923684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087865 | TGATAAGGACCCAAG[A/T]GGGCTGGTGACCAGA | 221178 |
rs189930423 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136066 | ATTTGCTCAGAGAGC[A/G]TGAAGCTCAGTTGGG | 221178 |
rs189931893 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048744 | ATATCAGAGTGCACT[C/G]TCATAAAGTGTCCCT | 221178 |
rs189939604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165205 | CCTGAAGCGGGACTG[C/G]CCTAGTCTTTGTGGA | 221178 |
rs190011271 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23983922 | GGCCTCACAAACATC[C/G]TGGCCGTGAAGGTAA | 221178 |
rs190018277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214019 | ATATGTTTGGTTTCA[A/G]AGGCATCCTTTGGGA | 221178 |
rs190032993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253098 | GGGTTCAGGTCCCAG[A/G]ATGGAAGATTCAGCT | 221178 |
rs190047975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233711 | AGTTTCAAAGTATTT[C/T]TGAAAGGGTGCTCAA | 221178 |
rs190050135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272706 | GACAGGCTCATAGCA[A/G]GATCGCTTTGCTGGC | 221178 |
rs190056788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080570 | GTCAGGCTGGACTCT[A/G]GGACCCATTAGTGTG | 221178 |
rs190064550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052905 | TCTGTGGAAAATTGT[C/T]TCACTTAGCTTCCTG | 221178 |
rs190070560 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070994 | TCCTTCCCTTTATGT[A/G]TATGTCTACGTCTGT | 221178 |
rs190078776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096043 | GCTAAGCCTGGTGGC[A/G]TCCTTTATCTCCCAG | 221178 |
rs190090936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011122 | CCTGACCACCTGGCC[A/G]TGGGCCCCTCCCTGT | 221178 |
rs190092424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991534 | TCTCCCTCACTGGGC[C/T]TCATGCTGCAAAGTT | 221178 |
rs190104781 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219262 | AAATTCCAGGAAAAG[A/G]CTTTTTTTCCATAAT | 221178 |
rs190115233 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246409 | GGGGAGGAAAAAAAC[A/G]TTTCCTCTACACTCT | 221178 |
rs190123265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285586 | GCAGTGATGTAATCT[C/T]GGCTCACTGCACCTC | 221178 |
rs190141495 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090570 | TACAGACTACTGAGC[A/G]TGGTTCTTTCCATTC | 221178 |
rs190147721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069567 | GTGTCTACAAACAGC[A/G]ATAATTTGCCATCCT | 221178 |
rs190169008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022519 | CAGTTTTGCAAGACA[A/G]AAACCTTCTGATCTC | 221178 |
rs190184067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027539 | GTATACTTGATCTCT[A/G]ATTTCACTGATTTTA | 221178 |
rs190205931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987294 | AGCTATTAGAATATG[C/T]CTATGACCGGGAAAT | 221178 |
rs190206622 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303774 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 221178 |
rs190210586 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24287636 | GACAGATGAGATCCT[A/G]AGTCATTTAGACACA | 221178 |
rs190213849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037092 | GCTGTCAATTTTAAA[C/T]TAATTGGCAGATAAC | 221178 |
rs190219450 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115335 | AACAGGGTCCCCAGC[C/G]CACAGACTGGCACTG | 221178 |
rs190223806 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110754 | AACTGAGCAATAATT[A/G]TAGAAACTGTAAAGC | 221178 |
rs190224188 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135147 | CAGGAAAATAAATTT[C/T]TATTGTATAAGCCAC | 221178 |
rs190234166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073420 | TATAAATATCTGTCT[A/G]TACCTATCTGTCATA | 221178 |
rs190242520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995084 | TCTCACCATACACAG[A/G]ACAGCCCCCAAACAC | 221178 |
rs190253807 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146829 | TATCTCCCAGATGGA[A/C]TGAGATTTCTTTACC | 221178 |
rs190258021 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209785 | GGATATATACCCAGT[A/T]TTGGGATTGCTGTAT | 221178 |
rs190259506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128309 | TGGCTTCATCACCAG[A/C]AATGCTCTGCCAGGT | 221178 |
rs190281314 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24250155 | ATATTTAGTAAGACT[A/C]CTGAAAGAAGTAATT | 221178 |
rs190286476 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169124 | GCATTGGGATCTCTG[C/T]GTGTCCTTGGGCCAC | 221178 |
rs190288605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185517 | TCTGGAAATAACTAC[C/T]CGTTTAATTTTAAAT | 221178 |
rs190291866 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230933 | TGGGGTTGATCAGAC[C/G]AGCTCTGTAGAGAGG | 221178 |
rs190299983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268014 | CCAGCTCCCAGTCAT[A/G]CTGATACTGCTGGTC | 221178 |
rs190307654 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277099 | TTTTGTTATGAAGCA[A/G]TAGACAACTCGCATG | 221178 |
rs190321954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111909 | TATGTTTCCTTGTTT[A/G]ATGTTGGTATTGAGG | 221178 |
rs190328176 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092601 | AGAAAGCCCATTTTA[C/G]GGTCTCTTAGAGATG | 221178 |
rs190344414 | snp | A/G | 0.0205944 | 0.0993632 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058963 | CATGGTCTGTGTATT[A/G]TTTTTTGTTTTGTTT | 221178 |
rs190355110 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174462 | TTATATGAGCATTTC[A/G]TGCTATCAGTTTCCC | 221178 |
rs190363885 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175859 | GGCTTCTATGCAGAG[C/T]GATTACTAGAAAACA | 221178 |
rs190368763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157555 | TCTGCCCGTCTTGGC[C/T]TCCCAAAGTGCTGGG | 221178 |
rs190370888 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137690 | CTTGAGCCTGGGGGG[C/T]GGAGGTTGCAGTGAG | 221178 |
rs190378396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209206 | AACACAGATGTGATC[A/G]CAGTGGTATCAAGAG | 221178 |
rs190384317 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230688 | CATGGGGCTTTGTAT[A/G]TAAGTTTCTAGCAAA | 221178 |
rs190388521 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191869 | AGTAATGAAAATGTT[A/G/T]CAGAATTTTGCTCCT | 221178 |
rs190395237 | snp | C/T | 0.000156777 | 0.00885233 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224795 | TAAATTGACAATGTA[C/T]GAGATTCATTGAGAT | 221178 |
rs190407140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188944 | GTTCCATAAATGGAA[C/T]AAAGCCTAGATGACA | 221178 |
rs190414789 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006578 | CCGGCCCAAGTACTA[A/G]TTCATCACAGTTGCA | 221178 |
rs190423266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072381 | AAATCAAGCATTTGT[A/G]TGAACTGGGAATATA | 221178 |
rs190431275 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044577 | ATAACGTACAGGGTA[C/G]AGTGTGATGTTTCAA | 221178 |
rs190437358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117469 | CTCACCATTTAGACA[A/G]TACTTCATCAAATAT | 221178 |
rs190438610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115054 | AGGGGAGGAGACAAG[A/G]TTTCTTGTTTGCCGT | 221178 |
rs190469997 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155233 | AGTGAAAGATGAAAG[C/G]GGGATTCTATGAAAG | 221178 |
rs190470408 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152498 | CCTCTTTGATAAGCT[C/G]CACCAGGGAGGTCCT | 221178 |
rs190476316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058626 | CTCATGGCTTCAAAA[C/T]GGTCTACATAATTAT | 221178 |
rs190479822 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295567 | CAGTGAGCCGTGATC[A/G]TGCCCCTGCACTCTA | 221178 |
rs190480504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091637 | CCAACATGGTGAAAC[C/T]TCGTTTCTACTAAAA | 221178 |
rs190508961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013551 | CCTTATCCTAAAAAG[A/G]TACTTTTTTCCTGAC | 221178 |
rs190541594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252170 | AATCCGAGATCAACA[C/T]GTCAGCAGGGTCAGT | 221178 |
rs190559007 | snp | C/T | 4.94474e-05 | 0.00497205 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290798 | TGACATCGCCATCGA[C/T]GGGTTCCTGCTCACA | 221178 |
rs190568382 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306875 | GTCATCTGTATAGGT[C/G]AAAGAATGGGACTTC | 221178 |
rs190569217 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293731 | GTCCCTGGTGTCATT[C/T]TTGCTCCTGCTCTCT | 221178 |
rs190599016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298259 | CCTTTGGCTGTGCCT[A/G]TGCAATACCTTCAGT | 221178 |
rs190605153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233966 | GCAGAATCTAAATAA[A/C]ATTATCGTATACCTG | 221178 |
rs190605928 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190126 | ATTATATAACATAAT[A/G]ATATACAATATATAT | 221178 |
rs190619393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273711 | ATACATATTTTAAAA[A/G]AGGTTAGTCTAACAT | 221178 |
rs190624260 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120459 | GGAGTTAAGTAAAAG[C/G]AGTTAAATTTCTCCA | 221178 |
rs190636354 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103051 | TTAAACAATTTTTTA[C/T]GAGGTAAAATGAAAA | 221178 |
rs190658051 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196904 | ATTGGATTGGCTAGA[A/G]AAAAAAACAGTTTGA | 221178 |
rs190703100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045922 | TGGGATCATAGTACC[C/T]ACCTCAATGGGCAAT | 221178 |
rs190711330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066475 | CAAGCCTAGGACTCT[C/T]GCCATGGTAGACCAG | 221178 |
rs190718327 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171875 | GGATTTGAAAGTTAA[A/G]GCAGTATATAATTGT | 221178 |
rs190725662 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085486 | CCAGAGGGGCAGTGC[C/T]GTCTGGAAGCCCTGC | 221178 |
rs190729809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007765 | GAGCCACCAAGCCCA[G/T]CCAGGGTTTTTTCAT | 221178 |
rs190732483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132132 | CCTTCTCCCTGGGCA[C/T]AGAGCTGGAATGCAG | 221178 |
rs190745217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024468 | GTTGTCTAGTGACAA[G/T]ACCAACCACATGCAA | 221178 |
rs190762403 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073909 | ACATAAATGGAAATT[A/C]TTGGAGATGTGCAGC | 221178 |
rs190790988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013948 | CTGTTTTAAGCTGTT[C/G]TGCTGTACTGACTCG | 221178 |
rs190791341 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037780 | TCTTAATCTGGGGTT[C/T]GTGGATTAGCTTATT | 221178 |
rs190802358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058861 | TTGTCTTTGAACATC[A/G]CCTTTCTTGGACAGC | 221178 |
rs190805665 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271173 | GTCAGTTGAAGAAAT[A/T]GGTTTTGTTTATGGC | 221178 |
rs190813466 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306455 | ATAAATGTCCTTTCA[C/T]CAGCTCACAGGCCAG | 221178 |
rs190833294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995521 | GCCCTAATTGGCAGC[C/T]GTTTTTAGCTCAAAA | 221178 |
rs190856963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253459 | GCAGTGCCTCTTCAG[C/T]GTTGATTAACTAGAG | 221178 |
rs190862195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101571 | CTATGCACATTCTCA[G/T]GCAGAAGATCCCCAG | 221178 |
rs190865488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291218 | GTAGTTAGTAAAGAC[A/G]GTTTCTGAGGGAAAC | 221178 |
rs190881107 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096460 | AAAAAATAGCTGGGC[A/G]TGGTGGCAGGCACCT | 221178 |
rs190899631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162839 | CTCACCAGACAGTGG[A/G]GCTTCCCTGCTGGGT | 221178 |
rs190901364 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181032 | GGCAGCTGTAACACA[A/T]TGGTAAGTGTTTCTG | 221178 |
rs190904861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116295 | CAGGCACTAGTCCCA[A/G]CCATGAGGACTCTGC | 221178 |
rs190907641 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062940 | CATCTGACAGTGCCA[A/G]GGCCTCCAAGTTCGC | 221178 |
rs190909969 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133244 | CTTCCTCTCTGCACA[A/G]GTTGAAGGGAAAGAG | 221178 |
rs190912947 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141839 | CAAGGGTAATAATGT[A/G]CTGTCTCAGAGCAGG | 221178 |
rs190914778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097271 | ATCATCCATTTAGTC[C/T]TCTCAGTCAGCCTGT | 221178 |
rs190917079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213489 | CCAGGCTGCTCTCAA[A/G]CTCCCGACCTCATGA | 221178 |
rs190921365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215053 | ATGTTCGAGCACAGC[A/G]TCTCCCTGAGGACGC | 221178 |
rs190926692 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233303 | TTGCAGGGACATTTG[C/T]CCTGATATGACAGTT | 221178 |
rs190929633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194347 | CATCCTGAGATTGCT[C/T]CTTTGCCTGGGACTT | 221178 |
rs190933569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182512 | AGAGAGAGAGAGAGC[A/G]CAGGAAAGAGGATGG | 221178 |
rs190942591 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186450 | AAACCAAGAGGGAAC[A/G]TCAGCCATAGTCCAG | 221178 |
rs190944012 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200147 | TAATTTAACCCAACT[A/G]CAGTTTGATGAATAC | 221178 |
rs190947943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169641 | GGGGGTCTGGCACAG[A/G]TGCCCAGTGTCGCTT | 221178 |
rs190949326 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996242 | CATGAGGGAGAGTCC[A/G]CCGCCTTGCCTTTCC | 221178 |
rs190953430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063747 | ATAAAACAAAATCAA[A/G]GAAAACAAAACAGAA | 221178 |
rs190959274 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237293 | TCTTGAACCCAGGGG[A/G]TGGAGGTTGCAGTGA | 221178 |
rs190961881 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081339 | ATTTTATTTTATTAT[C/G]TTTTTTTCCCACTTC | 221178 |
rs190964143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988862 | TTTATATTGGCTGTT[A/G]TTGAAAAATGTCCTT | 221178 |
rs190966012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123932 | CATTTCCTCTTTCAG[A/G]CTTTTGAGATAACCT | 221178 |
rs190973299 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002961 | TTTTTCTGAATGTGG[A/G]GGGTGAACAGAGAAA | 221178 |
rs190974178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258634 | AGATCGCACCACTGC[A/T]CCCAGCCTGGGCAAC | 221178 |
rs190980074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221235 | ATCCATCTGGTTGTC[C/T]GAAAAATGCAAGTCA | 221178 |
rs191016884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146995 | AGAAAACATCTTGGC[A/G]AGTCTTGAAATATGT | 221178 |
rs191019595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040893 | TTTGCTCAGGTTAGA[A/G]CACCACGAACTCAAA | 221178 |
rs191051104 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001318 | CGCTAAGGTCAGGAT[A/G]CCGGGGATAATGTGT | 221178 |
rs191086616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206199 | GGTCTAACATCCAAC[A/G]TCTACAAGGAACTTA | 221178 |
rs191095820 | snp | C/T | 0.0266618 | 0.112339 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181483 | TCCCTATTCCATAAT[C/T]TTTTTTTTATTAAAA | 221178 |
rs191098733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227915 | CTCTTGTACTTTTGT[A/T]TTCTTGAGATGGAAT | 221178 |
rs191103466 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295025 | ATTTCGAGGCATACT[A/G]TTGAATTTAACAGTC | 221178 |
rs191109209 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190091 | TATTATATAACATAT[A/G]ATGATATACAATATA | 221178 |
rs191117139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245245 | TACATTCCCTGGAAT[A/G]AACCTGGGTGGTATT | 221178 |
rs191127443 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285082 | ACGTGTGGAGCATAA[C/T]TCCTTAGTGAGTCAG | 221178 |
rs191131321 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264647 | CTATTAAGACAAAGA[A/C]AAAAGTTATATTCCT | 221178 |
rs191141661 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107055 | AGATGATAAGGACGG[A/C/G]GAAAAAAAAAAGGAA | 221178 |
rs191155949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153278 | CCTCTGATGTGGGTG[C/T]CCCATTTTCCACCTG | 221178 |
rs191165365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080767 | CTATGGCATGTGGAA[C/T]GTCCATCGCACATGT | 221178 |
rs191167790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115733 | GTGCTTCCGGTTCCA[C/G]ATTTCTCAGTGGGTT | 221178 |
rs191174233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142265 | ATACAAAGACTATCT[A/G]CTAGTCTACAGGCCT | 221178 |
rs191195719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041608 | CCATGGTGATGTTAA[A/G]GAAATGTTTTCTTTT | 221178 |
rs191208411 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262980 | AAAGAAACTTGACTG[A/G]GTCTTTTTTATAGAT | 221178 |
rs191219790 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24298857 | TCAGGCTAAAACGGA[A/G]GCAGGGATCGACTTG | 221178 |
rs191230007 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062622 | TTTTCTTATAGAAGT[C/T]GGGCTTCGGTGTGTC | 221178 |
rs191260499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014365 | CATGCAGAAATGGCC[C/G]CACTGTTTCTGGGGC | 221178 |
rs191261503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017344 | CCTACGTAAGCCCAC[A/G]TGCTTGACCTGAATT | 221178 |
rs191298550 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979244 | AAACTTGATTCCCAC[A/T]TCAGTCAGGATCTCT | 221178 |
rs191332891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202238 | TTTACTTTTTATCCT[A/G]GGATTTAAGTGCAAA | 221178 |
rs191337010 | snp | C/T | 0.00100432 | 0.0223864 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224108 | CGTGGCCCCCGGTTT[C/T]GGCTCAGCCACCTCT | 221178 |
rs191343121 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188312 | ACTCCAGCCTGGGCA[A/G]CAGAGCGAGACTCCA | 221178 |
rs191344657 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196396 | TTTAGTATGTAATAA[A/T]GCCTTAAATTATATA | 221178 |
rs191346313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220153 | AAGTGGGTATATGCA[C/T]AAATGTTGGTACCTC | 221178 |
rs191350448 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258243 | TCTATCTCAAAAAAA[A/T]AAAAATAAAAAGAAC | 221178 |
rs191356720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227372 | CAGGGTGATTTTGAC[C/T]ATTTTATGGTTTTAT | 221178 |
rs191357895 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192236 | CCAGGGACCCCCCTC[C/T]CCCCACACCTTATCT | 221178 |
rs191361349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294653 | TAGAGCATTCGTATA[C/T]GAAGAAGCGCCCCAG | 221178 |
rs191368129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280867 | TAGGTGACCTCCTGC[A/T]CTCCGACTGTACGCA | 221178 |
rs191372380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240461 | TTGGTTTTGGGGTCA[C/T]GGTGGTGACACGTGT | 221178 |
rs191378803 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304196 | TGTTCTTTATAAAAA[A/C]AGACCTTCACAAAAT | 221178 |
rs191380752 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261397 | GACCTATGGGCAGCT[C/T]GATGAAGATGACATC | 221178 |
rs191388478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089487 | AAAGACAGTTCTCCC[G/T]GTTCTGTATCTGATG | 221178 |
rs191403186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267584 | TGAGGCCAAGAGAGC[C/T]TTTGCTTTTTGAAAA | 221178 |
rs191407947 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302962 | CCTTTGTGGAAGGGA[A/G]GAGACGGTCATGACA | 221178 |
rs191409118 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163162 | AGCACTTTGGGAGGC[C/T]GAGGTAGGAGGATTG | 221178 |
rs191417300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124437 | CATAACAGAAGGACA[A/G]GGTGGATAGAAGGGC | 221178 |
rs191452875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176813 | TTTTCTTTTGAGATG[A/G]TGTCTTGCTGTGTCA | 221178 |
rs191504458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010721 | CTCCCCACTCCTCCC[C/T]CCCTCCTGCTCCTCC | 221178 |
rs191506041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065902 | GCTCTGCCACTTAAC[A/G]ATTTGACTTGTCTTG | 221178 |
rs191530335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020686 | GACATTTCAGTTAAA[C/T]TCAATGAATACTTTT | 221178 |
rs191531940 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071469 | TGTGAAGTGGGTCTG[A/T]TTGTAATTTACAGAT | 221178 |
rs191535687 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043715 | GCCAAAGGGAAAGGA[C/T]GAAATATTGGGCATG | 221178 |
rs191551487 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108324 | TCCTCTGATTCCCTT[C/T]GCACCTTTGCACCGA | 221178 |
rs191553259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982489 | AAAAATAAACTTTAC[C/T]GGACTGATGAAAACT | 221178 |
rs191561073 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089742 | GCTTTACCCATTTCT[A/G]CTGCCATAACAAAAT | 221178 |
rs191568069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054738 | TTTAATACTACCTCA[C/T]AGGAGAAAAGGTTAA | 221178 |
rs191574039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005724 | ACGAGCTGTAGAGGG[G/T]CATTTTCTGAGGAAT | 221178 |
rs191578757 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174211 | TTTTAAAGAAAGCGG[A/T]CCATTTTGTTGAAGT | 221178 |
rs191593381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154137 | TTTTGAAAAAAAAAG[A/C]TTGGCCGTAGCTACA | 221178 |
rs191596958 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237040 | AGTGTGTACATATAC[C/T]GCGGAATATTATTTA | 221178 |
rs191605282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277709 | ATCACATACTGAGTG[C/T]CTTCTGTATGCCAGG | 221178 |
rs191628295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206069 | CAACAAAAGCAAAAA[C/T]TGACAAATGGGATCT | 221178 |
rs191635090 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249027 | GACACGCGCCACCGC[A/G]CCCCGCTAATTTTTA | 221178 |
rs191642709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245134 | CCGTGGGCCCCGGCA[A/G]CCCACGCCGGAGTCT | 221178 |
rs191645077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072411 | AGATGATTAATGTTC[A/G]CATTGAGCCTGAGGC | 221178 |
rs191653663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284550 | CACCTGTAAACCCAG[C/T]TACTTGGGAGGCTGA | 221178 |
rs191656661 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090755 | TATTTATAATAGCTG[A/G]CTTAAAAACTTAAAT | 221178 |
rs191659250 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304997 | ATAACTGTAGGGGTC[C/T]CTGCTAGAGTTGTTT | 221178 |
rs191661631 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116701 | CAATCATCTCTGCAG[C/G]ATTAGGGGTTCACCA | 221178 |
rs191666031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993454 | TTGTCTGCACATTTA[C/T]GGCAATAAGGCTTCT | 221178 |
rs191671831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012884 | GGCTTGGGCTGGGCT[C/T]CCTCCTGTGGCTGGC | 221178 |
rs191673528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097955 | AGCCACTGTGGTTTT[A/G]AATACTACATGAAAA | 221178 |
rs191673747 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036465 | CTTGAGTTTCTTGAC[A/G]AGTGTGGTTTCTTAC | 221178 |
rs191698356 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185067 | CTTCTCCAGGGGACC[G/T]GCTCTGTCACTGCAT | 221178 |
rs191702463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092277 | ATGTTTTCTGGACAT[G/T]CCGGCAGCTCTCTAA | 221178 |
rs191710656 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130865 | TATAGGCTTAACATA[C/T]GTAATGTAAGGAGCC | 221178 |
rs191718972 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113887 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 221178 |
rs191719677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026156 | ATTCCCCTCAAAGTA[C/T]GATTTTTCATGTCGT | 221178 |
rs191725250 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167556 | CAGCCAGGTTCTAAA[A/G]TCGTGAAGTACCAAT | 221178 |
rs191726327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094285 | AAATGGGAACTCAGG[A/G]TTAACATAGAAAAAC | 221178 |
rs191729565 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077185 | TTAGGGTTCCATTCC[A/C]TAAGTTATCTGGAAC | 221178 |
rs191731292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067783 | GATCTCGGGTCACTG[A/C]AACCTCTGCCTCCCA | 221178 |
rs191737794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990378 | TGCCCTGGCTCACTC[C/T]CTCTGTTTCCTTGCT | 221178 |
rs191737887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127924 | CTCCTCATGCCTCCG[C/T]TGGCAGAATGATGAT | 221178 |
rs191738285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986423 | ACATGTGTTATCTGC[A/G]GGAAGAGGGTTTTGA | 221178 |
rs191837280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047154 | TGAGTCATGAGTCAC[A/G]GGTCAGGTGCAGTCA | 221178 |
rs191841226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170451 | CATCTCCTTCAGTTT[C/T]TCTCTCATTCTGGGA | 221178 |
rs191846722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187843 | CAATATTGAAAGTAG[A/G]CCAATTAATAACTCT | 221178 |
rs191851411 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149521 | AAGAGACAATCCCTG[A/G]TTGACTCTAGTGTTC | 221178 |
rs191857831 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986650 | ATGTTTAGAGGTGTG[A/G]ATTTCTCACCTTTAA | 221178 |
rs191860530 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24008374 | TGTCCAGCTGGAATG[G/T]CCAGGCCCTGTCCCT | 221178 |
rs191874616 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201004 | GGGCTTTGCACGCTC[A/G]TGTGAATTTTAAATT | 221178 |
rs191900366 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24289574 | ATTGCTATGAGGTAG[A/T]TATGATTATCTCTCA | 221178 |
rs191914202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248046 | TGGCCTGACTGACAG[A/C]CCTTTTTGTTTATAT | 221178 |
rs191927488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263918 | GGATTCCACAGAGTC[C/T]GAAGGAATTTAGAAA | 221178 |
rs191929994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136414 | CCAGGAGGCAGAGGT[C/T]GTAGTGAGCTGAGAT | 221178 |
rs191948491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175171 | AATCCTTTTGGTCGA[A/G]GGCATTAATCCTGCA | 221178 |
rs191955663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075172 | TTACTCTTCATCACA[A/G]CACTATTTTAAATCT | 221178 |
rs191956175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093808 | TGTGGTCATAATACT[C/T]AGAGGACTGTGTGTC | 221178 |
rs191957093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193374 | ACGGAGGCATTGTTG[A/G]CACAGGCGGTGGCCA | 221178 |
rs191960882 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112401 | ACAATCAATCCTACA[C/T]GTGTTTTATCTCCAA | 221178 |
rs191966071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299508 | GGCCTTGGAGGCAGG[A/G]ACAGCCCGGTGGCCA | 221178 |
rs191975688 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160004 | CAATTAATGATTAGG[C/T]CTTGAGCCTCACAAG | 221178 |
rs191977505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178350 | CATTATGATACGGCT[G/T]CAAGGAATGAGTAGA | 221178 |
rs191982416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111133 | CAGGCTGGTCTTGAA[C/G]CCCTGGTTTCAAGTG | 221178 |
rs191990571 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259824 | ATTATTATTATTTTA[G/T]ATTTTCTTTAGAGAC | 221178 |
rs191993308 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190010 | CATATAATAATATAT[C/T]ATTATATAACATAAT | 221178 |
rs191994046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211000 | TTTATTCTTTTCGAT[A/G]CTTTTGCAAATTTGA | 221178 |
rs191998264 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251164 | CTTCTTTCAACTAAA[A/G]CTCCACTGCCGTGTG | 221178 |
rs192002408 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278946 | TCCTTCCTTCCTTCC[C/T]TCCCTCCTTCCTTCC | 221178 |
rs192003052 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154029 | TTTTATGATTAGAAA[A/T]CTGAGGCTAAGACAA | 221178 |
rs192004085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231508 | ATCTGTTCATCTGTT[G/T]ATGGAGATGGGTTGT | 221178 |
rs192025345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146373 | CAACTCCTCTCCCTG[C/T]GGCCAGGCCAGATCA | 221178 |
rs192031948 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085937 | GAAGGCAGAGAAGCC[A/T]GAGAGGGTTTCCAGG | 221178 |
rs192032953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051892 | CCTAGGAGTTCCCCG[A/G]CACCTGTTCCTCCTC | 221178 |
rs192040824 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089123 | CAACCTTTTAACTAA[A/G]AACAGTTCCACAGGG | 221178 |
rs192043830 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139876 | ATCTAGACCATCCTG[C/G]CTAACATGGTGAAAC | 221178 |
rs192050292 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122416 | AGAGCAGTCTCTTCC[A/G]CATCATCTTCTTACC | 221178 |
rs192050568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008215 | TTTCAGTCACCTAAA[C/G]CTCTTGATGATCAGA | 221178 |
rs192089970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226702 | ATCCCTGGGGAGGAC[C/T]TCAGTTTTGTCTTAG | 221178 |
rs192119527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985564 | GCTCTGGTTGTGTCT[A/G]CCCCAGTGTGAGTCT | 221178 |
rs192170231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235167 | TGTACTTCTAAGTTA[C/T]AGCCGGAGCAAAGAC | 221178 |
rs192189338 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230459 | TGGGGTCTTTAGTGC[C/T]CCGGGCGGCGGTTGC | 221178 |
rs192191304 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098725 | CGAGGTCAAGAGATC[A/G]AGACCATCCTGGTCA | 221178 |
rs192206919 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059419 | TTTTCCACTTGATTT[C/G]CAGTCTCACTGGCTA | 221178 |
rs192210245 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174281 | CTTTTCAAAGAACAG[C/T]TCTTTGTTTAATTGA | 221178 |
rs192210988 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234736 | AGGGGCCCTGTGGAT[G/T]GGAGAGGATATAGCA | 221178 |
rs192214801 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266996 | TATGGTTTAGGTTTT[C/T]GTTGTAGGATTCTTA | 221178 |
rs192219314 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075980 | ATCTAGCAAATCATG[A/C/T]GGTGGAAACACCTTC | 221178 |
rs192235479 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998360 | TCTTGTTCTTATTTT[C/T]CATCTTTATCTTCTT | 221178 |
rs192235836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275761 | CAACATGGCGAAACC[C/T]CATCTCTACTAAAAA | 221178 |
rs192242009 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092881 | AACTAGAAGATTGCC[C/T]GAGTAAGCCTGAAAC | 221178 |
rs192245442 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038159 | ACCTCGTGATCCGCC[C/T]GCCTCGACCTCCGAA | 221178 |
rs192246366 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254980 | TCATCTCATGCTCTG[C/T]GGGTATTCTGAGGTA | 221178 |
rs192250307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292578 | ATTGTACCAGGAGGA[A/G]ATTTCTATGGCAAAC | 221178 |
rs192270515 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059220 | TCGTAATCCACCCCC[C/G]TCGGCCTCCTAAAGT | 221178 |
rs192275076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128874 | ACCAATTGATCTGGC[A/G]AGAAAACAAGTGAGC | 221178 |
rs192275095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190889 | GGTAAAATGCTATCA[A/G]ACAGTATCGCATCCT | 221178 |
rs192290201 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276574 | TTCTGTCGTACAAGA[A/G]TGTGAATATACTTGA | 221178 |
rs192292951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133750 | CAGAGCACAGGGGAG[A/G]AGAGGCAGAATAGTG | 221178 |
rs192302648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997764 | GAGGTGCCAGCCTCT[A/G]TAAACAACCAGCTCT | 221178 |
rs192322886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173506 | TATTCCCCCCCGTCC[C/T]CCAACTTTTTTTTTT | 221178 |
rs192379237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032486 | GTTGGAATCAGTTCA[A/G]CTCTGTCTCTGCCAG | 221178 |
rs192383480 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106522 | GTTGAGCAGTTGTGC[A/G]GCAGTGGCCAAGCCT | 221178 |
rs192391902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250697 | TATAACAAGCACTCA[A/G]AAACTCTTGCTTAAA | 221178 |
rs192392313 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070903 | AACTATGTCCTCAGC[A/T]CTCCCAGGTTTCCAG | 221178 |
rs192395434 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288239 | AGAAGTTAAGTGGTG[A/G]GATTGGATTTAAACC | 221178 |
rs192437359 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064350 | AATCAATGGGAGAGC[A/C]GTAACCTCACAGTGG | 221178 |
rs192440954 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158518 | CACAGCTGGTTAGAG[C/T]CAGGTTGGACTGCGC | 221178 |
rs192453312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035137 | CCTATACTTATTGGG[C/T]ATTGTTTACTTTCTA | 221178 |
rs192456406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139082 | GTGCTCTGACAGCTC[C/T]GGGGGTGCATCCTTC | 221178 |
rs192457942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121918 | GCCAGGTTGCATGAT[C/T]GGGTCCCATCTCCTG | 221178 |
rs192471452 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243611 | TTAATCAGTAAAATT[A/C]TGTGAAGAGTACCTG | 221178 |
rs192482615 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069042 | ATATTCTTGCGTAGT[A/G]TAGTCAGGTAGCGTA | 221178 |
rs192486106 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992168 | GTTCTTGGTAGAAAG[C/T]GGAGAACTGCAGTCC | 221178 |
rs192503341 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104383 | CCACTCAATTTTTAG[A/G]GAGGTTTGGTTTTAC | 221178 |
rs192503906 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095443 | GGGGAGTTAAATTTA[A/G]CGGGTACAGAGTTTT | 221178 |
rs192505346 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027158 | TTTTTTTTTTGAGAC[A/G]GAGTCTAGCTCGGTC | 221178 |
rs192509412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087258 | GGGGCCTGGGACCTC[A/C]CCAGTCTTGCCTGAG | 221178 |
rs192512517 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047608 | GCTTTAGTAAATCCT[A/G]TTAGTTTTCCAAAGT | 221178 |
rs192525279 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037424 | TATTTATTTATCTAT[C/T]TGAGATAGAGTCTCG | 221178 |
rs192539015 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144013 | TTGGCCAGAAACACT[C/G]AAAGCACGTAGAGTG | 221178 |
rs192541621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217193 | AGTCTAAGAATTTGA[A/G]GCCACCCCGGGCAAC | 221178 |
rs192541842 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004249 | AGCAGATACACAATT[A/T]TGCTCTGCAGTCATC | 221178 |
rs192544402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098936 | ATCTCAAAAAAAAAA[A/G]AAAAAAGAAAAAAGA | 221178 |
rs192580833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117018 | TGGACTTCCCAGCCT[C/T]CAGAACTCTGAAAAG | 221178 |
rs192586986 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980601 | GAAGTTTTGTTTTGT[G/T]TTGTTCGTTTTGAGA | 221178 |
rs192607392 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083035 | TAGCCCAAGCCTTCT[A/G]TGCTGGACTAGAAAT | 221178 |
rs192610825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154577 | GCTAGAAATTTTCAG[C/T]ATTTTCATGTTGTAT | 221178 |
rs192629928 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144561 | ACTGGCCCAGACAAA[C/T]TTTGATCAGGCACCG | 221178 |
rs192640514 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109911 | GAATCAAAGGTGGCA[C/T]CTTTTTAAGGCTTTC | 221178 |
rs192647295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183570 | GCCCAACACAAATTC[A/G]TAAACTTTCTCAAAA | 221178 |
rs192649246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300627 | AGAACAGGGGCCAGG[C/T]GAAGGTGGCCTGTGT | 221178 |
rs192658755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197270 | AAATTTTGACACAAC[A/T]GAGACTCAGTAGGAA | 221178 |
rs192664770 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135156 | AAATTTCTATTGTAT[A/G]AGCCACCTAGCTCGT | 221178 |
rs192668481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183020 | GCTTCTGAGGATATC[C/T]GCTTACATATATTCC | 221178 |
rs192670026 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164039 | TGTTTTAGAAAGAAC[C/T]ATCATTGTTATTTCT | 221178 |
rs192670194 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117528 | TTTTGATTCATTCCT[A/G]CATAGATCTGGGCAA | 221178 |
rs192674348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234159 | ACCATTTGTAATCAA[C/T]TTGTCATGATGTACT | 221178 |
rs192681457 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256239 | AAAGGTTGGTAAATG[A/G]ATATAAAAATAGAGC | 221178 |
rs192689205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253805 | AGAAGCCCAAAGACA[A/G]GCAGGAAACATGATG | 221178 |
rs192694140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293589 | ATTTCCTTGTCTTAA[A/G]TAAAACAAAGCAAAA | 221178 |
rs192694828 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042992 | GGGTTGAGAATGAAC[A/C]CTTTCGCAATGTGTG | 221178 |
rs192695630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215769 | GCTCCAGATTTGGGC[C/T]AGTCTGCCTCTGCCA | 221178 |
rs192705109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082582 | TCCCAGCACTTTGGG[A/G]GGCCGAGGCGGGTGG | 221178 |
rs192706905 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121244 | ATTTTTAGCAGCAAT[A/G]AAATACCACTAAACC | 221178 |
rs192717310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086510 | TATGGGAAAAATATG[A/G]AAGAAAGGATGAATT | 221178 |
rs192728308 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157839 | AACAGGAGCATGAGA[C/T]CAAATCCTGGCTCCA | 221178 |
rs192729455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060446 | CTCAAGAGGGATTAA[A/T]AACTTAAATGTAAAA | 221178 |
rs192741112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016499 | ATGATGCAGGCCACA[A/G]CCACAATGCTAGGCT | 221178 |
rs192748112 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268372 | TGAGCCTATAATTTA[A/G]TAAACTACCACCTTT | 221178 |
rs192749761 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231174 | AATTCAGTGATTTTT[A/T]TATGTTTATGGAGCT | 221178 |
rs192756829 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260846 | TTCTAGTCAGTTGAT[C/T]GTACACAGGGAGCCT | 221178 |
rs192771157 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295890 | TAAATAACTTGCCCA[A/C]GACCACACAGCTCAA | 221178 |
rs192778717 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011542 | GCTGATGCCCTCCAG[C/T]TGTGGGCTGGCCATG | 221178 |
rs192794491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222239 | TTGCTGAGTCCTTCC[A/C]GCCTGTGTCTAGGTG | 221178 |
rs192807907 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238310 | TACAAGTGTGCACCA[C/G]CATGCCCGGCTAATT | 221178 |
rs192810656 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200506 | CCCACCTCGTTCTCA[C/G]CCCCAAGTCTCCCAC | 221178 |
rs192820604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981447 | TTGAGAGCAGAGAGA[G/T]AAGTGGTGAGAAGAA | 221178 |
rs192824400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019537 | CAAATATTTATGTGT[A/G]TTTTAAAGCATTTTT | 221178 |
rs192829949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104826 | TTCTTAGCCTGGCTG[C/T]AGCCTCCTCTCCAGT | 221178 |
rs192833409 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129682 | TTTCTGTCTGTTTCT[G/T]CTTTAAATAGGCTGT | 221178 |
rs192844954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069640 | TTGCCCTGGCCAGGA[C/T]TTAACTTTGTTTTTA | 221178 |
rs192852073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169991 | TTATTTTAAATGTGA[C/T]GTCTTCATACAAAGT | 221178 |
rs192866910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126461 | GTCCCTTAAAACCCA[C/T]GACAATTGTGTCTAT | 221178 |
rs192882011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269186 | GTGAGGATTATTGAT[G/T]GGTGCTGCAGTTATC | 221178 |
rs192885965 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304846 | TGTGGCATGTGTGGG[A/G]GTGTGTGTGTGTATG | 221178 |
rs192887398 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164426 | CTCCATACCAGCCTG[C/T]CTTGACAGAATGAAA | 221178 |
rs192907033 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064051 | ATCTTCTTCAAGTCA[A/G]CCATTTCTCTCTTTG | 221178 |
rs192926050 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039177 | AATAAAACGTTCATG[G/T]TGTATGATGTCACCA | 221178 |
rs192933195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138384 | ACAAATTCTGTATTT[C/T]CTCCAGTAGGGGTTT | 221178 |
rs192937883 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216381 | AACACCATTCTCACC[A/C]ACAGGAATGTGTTTT | 221178 |
rs192941387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999278 | TCAAAATCAAGTGCT[A/G]TAGGTCCTCCATTTT | 221178 |
rs192948875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067970 | TGGCCTCCCAAAGTG[C/T]TAGGATTATAGTTGT | 221178 |
rs192968334 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238855 | TACTGGAAATATTTG[A/G]CAGCAGAACACATTA | 221178 |
rs192972325 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24279387 | CCCTGTGGATGATTC[C/T]GAGCAGAGGAGTGAC | 221178 |
rs193012790 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038073 | CCTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 221178 |
rs193022524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221734 | GCATGGGTGCAGTAG[C/T]GTGTGGTTGTCAGGG | 221178 |
rs193040267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087931 | CACTGGCTGCAGCCC[C/T]TGAGGTCAGCCAGCC | 221178 |
rs193044382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113497 | TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCATG | 221178 |
rs193052799 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186818 | GGGAAGGAAGAGCTG[A/G]AAATAGGATTGGAAA | 221178 |
rs193058017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148316 | TACTTTCATGAGCCC[C/T]GTTGTCTTTTGTGCA | 221178 |
rs193070732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210744 | CGTCTGGAATCTTTT[A/G]TGGTTCTATATGAAT | 221178 |
rs193071016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177524 | CAGTCTTACTCTGCA[A/G]TCGTAGTTCACTGGA | 221178 |
rs193073912 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150176 | TGTCCTGAGACACAT[C/T]GGCTCTACAGTGCCC | 221178 |
rs193086563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288797 | CCTAAATCCAACCGC[A/G]TGAGCCTTTTTGCTT | 221178 |
rs193091814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009365 | TGTAAAATATTTGAA[A/G]GGATTCATTCTGAGC | 221178 |
rs193098592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090336 | TCCCCTTTCATAGCT[C/T]CAGCCCATCCCTGTC | 221178 |
rs193104977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054925 | CCCAGCATTTAAACA[C/T]TAAGTCAATTTAGCT | 221178 |
rs193109611 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125277 | CATCTCCTAACACGG[C/G/T]GGGAGAGGGAGGAGC | 221178 |
rs193113788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011982 | CACAGGCACAGGGAC[C/T]GGGGCTTGCCCACCA | 221178 |
rs193129413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228839 | TAAATATTATAATGT[A/G]CTTTCAATAGGGAGA | 221178 |
rs193129812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265167 | TGTATGATGGGGCCC[A/G]CCCCTCCTGTGGTGA | 221178 |
rs193130201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291877 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 221178 |
rs193141120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155268 | ATGTGCCTCTGTGGT[A/G]CTCCATCCCCAGTGA | 221178 |
rs193151661 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190132 | TAACATAATAATATA[C/T]AATATATATTATTAT | 221178 |
rs193171197 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198047 | GTCGCCCAGGCTGGA[G/T]TGCAGTGGCATGATC | 221178 |
rs193185442 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048884 | AATAGCTTCAGATAA[C/T]TTCTTTATTATAGAA | 221178 |
rs193206446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015609 | ACTCTCACCATTGCC[C/T]ACTCATGGGGCTTCT | 221178 |
rs193210127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987138 | ACCTGTTAGTAAAAT[A/G]AGACATTCATTTATA | 221178 |
rs193236118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193226 | TGAGGGGGAAGTGAC[A/G]GAGCTCTGAGGAAGG | 221178 |
rs193237834 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171242 | TGAGGCACTTGGAAA[A/G]CAGTGCCCATCACTG | 221178 |
rs193262194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071599 | TGGTCTGACTCAGCC[C/G]TCTGTAGTATGGAGC | 221178 |
rs193265828 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108474 | GAGTGCAGCCCTAGG[A/G]TGGGAGCCTGCCTGG | 221178 |
rs193269224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035637 | CTGATTCACAGGAGG[C/T]GTGTCACTGAGTTGT | 221178 |
rs193278207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245954 | TTAAAAGAATGATCC[C/T]GAGTCCTGCCCGCTG | 221178 |
rs193280224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274269 | TAAGTAAGCTTAACC[G/T]GAAGGTCCAGTGGTT | 221178 |
rs193298596 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206745 | AAAAATACAAAAATT[A/T]GCCAGACGTGTTGGG | 221178 |
rs193300557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174499 | CACTGCTTTCGCTAT[A/G]TTCCACACATTTTTA | 221178 |
rs199519307 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048462 | TTTAGTAGATCTAGT[A/T]AACTAATCAAGGATG | 221178 |
rs199534021 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202963 | TGAGATTTTTTTTTT[-/T]CCCTCAAGTTTTATT | 221178 |
rs199554673 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142637 | TTCAACAACTTTTTT[-/T]CCTCCTCCCCCTTTC | 221178 |
rs199573730 | in-del | -/TACGTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189492 | CTCTCTCTATATATA[-/TACGTG]TATATATATATATAA | 221178 |
rs199576949 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024356 | GGATGAATGGATGGA[C/T]GGATGGATGGATGGA | 221178 |
rs199580047 | in-del | -/T | 0.260005 | 0.2498 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254819 | TTTCTTGCTTGCTTC[-/T]TTTTTTTTTTCCTTT | 221178 |
rs199595659 | snp | A/G | 0.000482879 | 0.0155308 | missense | SPATA13 | GRCh38.p7 | 13:24284155 | TCAGATGGAGGTACT[A/G]AGCCCTCTGCCTTAG | 221178 |
rs199613715 | snp | A/G | 6.60153e-05 | 0.00574485 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24289046 | AATGTTCACCGTTGC[A/G]CAGCTAGCCACTATT | 221178 |
rs199614790 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286915 | ATCATGGACACCGAG[C/T]GGGTGTACATCAAAC | 221178 |
rs199660209 | snp | A/G | 0.0039921 | 0.0444985 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223812 | CTGAGCAGTTCCTCC[A/G]CTGACTCCCAAAAGC | 221178 |
rs199664552 | snp | C/T | 0.000187003 | 0.00966782 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223625 | CACTGGCCAGGTGCC[C/T]GCCGTGTGTGAGATT | 221178 |
rs199680840 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291759 | TTTTATTTTTTTATT[A/T]TTTTTTTTGAGACGG | 221178 |
rs199698867 | in-del | -/AC/CG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189493 | CTCTCTATATATATA[-/AC/CG]CGTGTATATATATAT | 221178 |
rs199719200 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042444 | AGTGCTTCTGTTTCC[A/C]AAGCAAACCAGGCTG | 221178 |
rs199725274 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196875 | GAGAAGCATGATTTC[C/T]AACACTCTAGAATAT | 221178 |
rs199726611 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161933 | CCAGCGATTTGCTCT[C/T]CTTTATTCCCCTTGC | 221178 |
rs199747226 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216202 | TCGCACAAGCTCAGA[-/C]CCTACCTGCCCTTTC | 221178 |
rs199770674 | snp | A/G | 3.29495e-05 | 0.00405877 | missense | SPATA13 | GRCh38.p7 | 13:24297618 | AATGCCTTCAAGCTC[A/G]TCAGTAGGACCACAG | 221178 |
rs199771606 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204378 | TAACTGGTAAATTGT[G/T]TTAAAAGCATTGTTT | 221178 |
rs199773072 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156122 | CACCTTGTGGCTGTG[G/T]GAATACTGCTGCTAT | 221178 |
rs199786470 | in-del | -/T/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185735 | GCAGTTTTTTTTTTT[-/T/TT]CATGAGCCCTGTGTT | 221178 |
rs199788481 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258681 | TCCGCTAAAAAAAAA[C/T]AGAGACTGAAAAGTT | 221178 |
rs199793559 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240994 | GTTGCTTCTTTTTTT[G/T]TTTTTTGGAGACTCT | 221178 |
rs199814604 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076386 | ATCAATGGGAAAGCA[C/T]ATCTGCAACTGGGCA | 221178 |
rs199815880 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015815 | TGAGCCTCGGCTGGT[A/G]ACACGTCATAGTCCC | 221178 |
rs199821527 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128736 | AGTCCTACCTTATTT[-/AA]AAAAAAAAAAAAAAC | 221178 |
rs199873706 | in-del | -/TC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126539 | GTATATATATTTGTG[-/TC]TGTGTGTGAGAGAGA | 221178 |
rs199875275 | in-del | -/TA | 0.259674 | 0.249813 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189953 | TATTACATAATATAT[-/TA]TATATAATTATAAAA | 221178 |
rs199882330 | in-del | -/TT | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988724 | TGGTTTTAGTTTACA[-/TT]TCTCCTATTTTGAAT | 221178 |
rs199885622 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269392 | TATGTATGTATGTGT[C/G]TATGTATGTATGTAT | 221178 |
rs199886090 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24218719 | GGGGTTTTTTTTTTT[-/T]GCGATTTTTTTTTTA | 221178 |
rs199892055 | snp | A/G | 0.000283768 | 0.0119081 | missense | SPATA13 | GRCh38.p7 | 13:24249828 | ACGGAGGAACTGGAC[A/G]ATCTTCTGACCCAAG | 221178 |
rs199895551 | in-del | -/ATT | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196292 | ATAAACCCTTCACAC[-/ATT]ATTACCTGGAAGTAT | 221178 |
rs199897796 | in-del | -/AAAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277460 | AAAAAAAAAAAAAAA[-/AAAG]AAGAAGTTCACCTTG | 221178 |
rs199921174 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054417 | TACTGGCAGTGGCAG[A/C]GGTGGCATTAGAAAT | 221178 |
rs199946437 | snp | C/T | 5.08539e-05 | 0.00504226 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24284244 | TCGGTACCTGCAGCC[C/T]GGCGGGGAGCAGCTG | 221178 |
rs199952947 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181761 | CTGTTTTACAGTTGA[C/T]TTTTTTTTTTTTTGT | 221178 |
rs199955402 | in-del | -/CAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052382 | CATCGCTACAAACAA[-/CAA]GAACAACAACAACAA | 221178 |
rs199963629 | in-del | -/ATC/ATG | 0.440609 | 0.161766 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190154 | ATTATTATATAACAT[-/ATC/ATG]ATATATAATATATAT | 221178 |
rs199969340 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210473 | CAATTTTATTATTTT[A/G]CATGTGGATATTCAG | 221178 |
rs199972084 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189499 | TATATATATACGTGT[A/G]TATATATATATAATA | 221178 |
rs199972523 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24045124 | ATGTATAATTTATAT[A/G]ACTCATTGCCAATCC | 221178 |
rs199977292 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173503 | TTTATTCCCCCCCGT[-/C]CCCCCAACTTTTTTT | 221178 |
rs199983720 | in-del | -/T | 0.020034 | 0.0980594 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181484 | CCCTATTCCATAATC[-/T]TTTTTTTATTAAAAT | 221178 |
rs199986340 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276654 | AAAGGAAGAAAGAAA[C/G]AATAAAATTTACTTT | 221178 |
rs200013571 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121024 | CTTGCTTTTCTTTTC[C/T]TTTTTTTTCTGAATT | 221178 |
rs200040597 | snp | A/C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278941 | CTCTTTCCTTCCTTC[A/C/T]TTCCTTCCCTCCTTC | 221178 |
rs200053367 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074497 | AGCACATTTAATTGT[A/T]CTCATGATGACTGTC | 221178 |
rs200057049 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043321 | TGGTGGATGCTACCC[C/T]TTTTTGTGGTCAAAC | 221178 |
rs200057604 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157299 | TTTTTCTTTTTTTTC[C/T]TTTTAATATATTTTT | 221178 |
rs200090739 | in-del | -/A | 0.110167 | 0.207236 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159103 | TTCTAAAGAGATAAT[-/A]AAAAAAACCCTCAAT | 221178 |
rs200097566 | in-del | -/TA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067344 | TGAGCTATATGTATG[-/TA]CCCTTTGTAAGTCAA | 221178 |
rs200111487 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999611 | TCAGGGTGGATTCTT[C/T]TGCCTGAGCTGCAGC | 221178 |
rs200129955 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980898 | GCCTGGCCAACAAAG[-/T]TTTTTTAAAAAATAC | 221178 |
rs200131511 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052504 | ATGTTTTTTTTTTTC[C/T]TTTAAACCCATGATG | 221178 |
rs200138056 | in-del | -/CCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997870 | TGAGCCAAACACTTC[-/CCA]CTAGGCCCCATCTCC | 221178 |
rs200138957 | snp | A/G | 0.000197782 | 0.00994242 | missense | SPATA13 | GRCh38.p7 | 13:24302766 | GGCTCACCCCCTTCC[A/G]GAAATGAAAACAGGA | 221178 |
rs200141542 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151932 | TTGCCCAGGATGAGG[A/G]CTGCAAAGGGAGAGA | 221178 |
rs200145805 | snp | C/T | 0.00092448 | 0.0214799 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284288 | TACTGGAATTCCACA[C/T]GACAGTAGTGGATAC | 221178 |
rs200155235 | snp | A/G | 0.000156632 | 0.00884825 | intron-variant, missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270901 | TCTGGAGTCTGGAAA[A/G]CCTTCACTTGGGTAT | 221178 |
rs200155593 | in-del | -/AATTGTAAAGC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197288 | GACTCAGTAGGAAGA[-/AATTGTAAAGC]TGGAAAGAGTAAACA | 221178 |
rs200156236 | in-del | -/C | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198236 | TGACCTTGTGATCTG[-/C]CCCCCCTTGGCCTCC | 221178 |
rs200161815 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052445 | AAAATTCAGAATGAC[C/G]AACACTTTCATTCAG | 221178 |
rs200203716 | in-del | -/TATAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140729 | CAAGAATGTTAGTAT[-/TATAT]AATGAAGTGAACCCA | 221178 |
rs200235625 | snp | C/T | | | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160697 | TGGCCTGGTGGGGAG[C/T]GGGGCTGGGGCGTGG | 221178 |
rs200236189 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136829 | TATGTTCTTTATTTT[A/T]TTTATTTATTTTTTT | 221178 |
rs200244378 | snp | G/T | 1.67435e-05 | 0.00289335 | missense | SPATA13 | GRCh38.p7 | 13:24286373 | GATAAGGAAGCCTGG[G/T]TCCCCGCGAGCTTCG | 221178 |
rs200284685 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190451 | GGCAAAGTAAAGTGA[A/C]AACCTTCTGGAACTG | 221178 |
rs200286610 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24177706 | ATCCTTCCACCTTGG[C/T]CTCCCAAAGTGTTGG | 221178 |
rs200291159 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24141173 | AGTGAGACTCTGGCT[A/C]AAAAAAAAAAAAGAA | 221178 |
rs200298148 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171506 | AGATGACAGTGGGAG[G/T]GCCACAAGGATGGGT | 221178 |
rs200310974 | snp | C/T | 1.68946e-05 | 0.00290638 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251879 | TGAGTCTCAGAGTCC[C/T]TTTCCTTTCAGAGCT | 221178 |
rs200325226 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993146 | GAACCTGCTGTGGCG[-/A]AAGGTCGTGGACAGA | 221178 |
rs200326744 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24263683 | AGTTACAAGAAAAAA[A/C]GTCTGTACATATTCA | 221178 |
rs200343068 | snp | C/G | 0.380138 | 0.213458 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190216 | TATTATATAACATAT[C/G]ATATATAATATATAT | 221178 |
rs200388348 | in-del | -/TAAATAAATAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202071 | GAGCAAGACTCTGTC[-/TAAATAAATAAA]TAAATAAATAAATAA | 221178 |
rs200399567 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221484 | GAAAGGTTAAGGGGG[-/A]GCAGGATTTTCATTT | 221178 |
rs200420134 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024360 | GAATGGATGGACGGA[C/T]GGATGGATGGATGGA | 221178 |
rs200421129 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248883 | GATGGTGCTGATTTT[C/T]TTTTTTTTTTTTTTG | 221178 |
rs200422744 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108663 | GCTTTTCATGGTAGG[C/G]GGGGGGAAGCCTGAT | 221178 |
rs200425368 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987846 | GTACCTCTTACAAGC[A/G]GATTCTATAGTATTT | 221178 |
rs200434192 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043674 | GTAACTTTGAGGGAA[A/T]TTTTTTTTGTTGTTG | 221178 |
rs200439490 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24031052 | ACCGCATTTTCTTCC[A/G]TTTCTCAATATCTTC | 221178 |
rs200464532 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208576 | GATCAAGAAGACTGG[G/T]GGGGACTTTCCAGAC | 221178 |
rs200472890 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237377 | AAAACAAAACAAAAC[-/A]AAAAAAAACATGCTG | 221178 |
rs200487636 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077624 | GGATCTAAAATAAAA[-/T]TTAAAAAAAAAAGAC | 221178 |
rs200502574 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100551 | TGATGGAATGTTCTG[A/T]CACATGAAGATGATT | 221178 |
rs200527880 | in-del | -/AACT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048462 | TTAGTAGATCTAGTA[-/AACT]AACTAATCAAGGATG | 221178 |
rs200531030 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181089 | AATACGGTATAAAAG[-/T]TTTTTTTTTTAAATG | 221178 |
rs200532783 | in-del | -/AT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030090 | CACACACACACACAC[-/AT]ACATACATACATACA | 221178 |
rs200545517 | in-del | -/GAAT | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979244 | AACTTGATTCCCACT[-/GAAT]TCAGTCAGGATCTCT | 221178 |
rs200551712 | in-del | -/ATT | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044719 | TGAAATATACAGTAC[-/ATT]ATTGTTAACTATAGT | 221178 |
rs200553144 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24028961 | CTAATAATTTTACTT[C/T]CTAAAGTCCTGGTGA | 221178 |
rs200556813 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040454 | GAAATTCACAGCACC[-/A]GCCCTTGACAGGAAA | 221178 |
rs200561905 | snp | A/G | 0.00131666 | 0.0256241 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224347 | CACCCAAGCCCCAGA[A/G]CCCTCAGAGCCCCCA | 221178 |
rs200561968 | snp | C/G/T | 0.000743082 | 0.0192625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294881 | GAGGTAAGTGGAAAG[C/G/T]ACCCCACATGATCCC | 221178 |
rs200562863 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048469 | GATCTAGTAAACTAA[G/T]CAAGGATGAAGAGGA | 221178 |
rs200583620 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057058 | CGTCTGGCTCTTTCT[-/C]TTTTTTTTTTTCTTT | 221178 |
rs200594444 | in-del | -/TTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019072 | TCCTAAGTTATATGA[-/TTC]TTCTTATTATTATTA | 221178 |
rs200594808 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150879 | CCTAAAAATACCTTC[A/C]CAGCCACACGGAGAC | 221178 |
rs200607783 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24061866 | AACCTAACATAAAAG[-/T]TTTTTAAAAAAAATT | 221178 |
rs200642921 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278906 | TCCTTCCTTCCTTCC[A/T]TCCTTCCTTCCTTCC | 221178 |
rs200648645 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201044 | AGTCACACACACACA[C/G]ACACACACACACACA | 221178 |
rs200650657 | in-del | -/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188149 | GTTCGAGACCAGCCT[-/G]GGGCAACATGGTGAA | 221178 |
rs200677895 | in-del | -/TGTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24049080 | TAAAAAGATAAGAAA[-/TGTC]TAAAGTCTTCTAACC | 221178 |
rs200683336 | in-del | -/CGTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189494 | CTCTCTATATATATA[-/CGTG]TATATATATATATAA | 221178 |
rs200690838 | in-del | -/GTGATCCGCCCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026813 | GGATCTCCTGACCTC[-/GTGATCCGCCCTT]GTGATCCTGACCTTG | 221178 |
rs200699863 | in-del | -/A | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978863 | CACACCCAACTAATT[-/A]AAAAAAATTTTTTTT | 221178 |
rs200701369 | snp | C/T | 0.000235845 | 0.0108567 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24284217 | CTATGAAGACCTCTG[C/T]CAGGCCAGCCCTCGG | 221178 |
rs200703541 | in-del | -/TAGCTGGCTCCCTGCTGCC | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281036 | GGGTACACACATGCA[-/TAGCTGGCTCCCTGCTGCC]CACCCACCCGTGCTC | 221178 |
rs200720706 | in-del | -/C | 0.0232847 | 0.105357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114959 | AGCCACTACACCCAG[-/C]CCCCTTGGCTTTGTT | 221178 |
rs200730187 | in-del | -/ACG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124268 | TAGTAGTCTATTGAC[-/ACG]ACCACCTTAGAATCT | 221178 |
rs200739895 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276657 | GGAAGAAAGAAACAA[A/T]AAAATTTACTTTTTA | 221178 |
rs200761258 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044906 | GTGGGGGTGGGGGTA[-/G]GCAGAGTGAAGAGAG | 221178 |
rs200769497 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24016178 | TTGTGTTTGTGGCTT[G/T]TCCTTCAACCCCACT | 221178 |
rs200777439 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074741 | TTTAGCAGAGTTTAA[C/T]TGAGCAGAGGAAGAT | 221178 |
rs200781413 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201616 | CAGCTAATTTTTGTG[G/T]TTTTAGTAGAGACAG | 221178 |
rs200783275 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206289 | ACTAAAGAAGACACA[C/T]GTGGCCACAAAACAT | 221178 |
rs200809246 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083219 | CCAGTGGAGACCCCC[-/C]TAGGGCAATAGAATA | 221178 |
rs200832943 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208704 | GCCCATAGGCCAAAA[A/G]AAATCCCTGACAGTT | 221178 |
rs200833182 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193933 | CATTGTGATGAGTTT[A/G]GAAGGGTGGAAGCTT | 221178 |
rs200837147 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019095 | ATTATTATTATTATT[-/A]TTTTTTTTTTTGAGA | 221178 |
rs200851222 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074498 | GCACATTTAATTGTA[C/G]TCATGATGACTGTCC | 221178 |
rs200858196 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052502 | ATATGTTTTTTTTTT[C/T]CTTTTAAACCCATGA | 221178 |
rs200898138 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081720 | TAAATTTAAAAAAAA[A/T]TAAAAATTGCACACT | 221178 |
rs200899985 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204379 | AACTGGTAAATTGTT[A/T]TAAAAGCATTGTTTT | 221178 |
rs200900992 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211913 | TTAGAGCATCCGTGT[-/GT]GTCGGCTGAAGGAGG | 221178 |
rs200903972 | snp | C/T | 0.000829546 | 0.0203491 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302583 | CTGTTCCATCTCTCT[C/T]CCCTCCCGAGTCAGG | 221178 |
rs200917406 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170250 | CTGAGGGCTACTTTT[-/A]AAGCCTGCTGTGATT | 221178 |
rs200921316 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24294615 | AGGGAAACAGTGGCT[A/T]ATGACGTAAATGTCA | 221178 |
rs200942393 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019093 | ATTATTATTATTATT[A/T]TTTTTTTTTTTTTGA | 221178 |
rs200954083 | snp | C/T | 1.67863e-05 | 0.00289704 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294724 | TGTGATTAAAATTAA[C/T]CTCCCATCTTGCAGT | 221178 |
rs200968438 | in-del | -/TGTGTGTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173363 | TCATTAGTTCTTAGT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 221178 |
rs200977526 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24163282 | CGCACTCACCTGTAG[-/T]TCCAAGGTGCTCAGG | 221178 |
rs200981454 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067343 | CTGAGCTATATGTAT[G/T]TACCCTTTGTAAGTC | 221178 |
rs200988932 | snp | C/T | 0.260227 | 0.249791 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030091 | ACACACACACACACA[C/T]ACATACATACATACA | 221178 |
rs200999275 | in-del | -/AT | 0.305436 | 0.243776 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190020 | ATATTATTATATAAC[-/AT]ATAATGATATACAAT | 221178 |
rs201000938 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275099 | CAATCCTTCCAATTT[A/T]AAAAAATGACACCTC | 221178 |
rs201006373 | snp | C/G | 8.42396e-05 | 0.00648943 | missense | SPATA13 | GRCh38.p7 | 13:24284227 | CTCTGCCAGGCCAGC[C/G]CTCGGTACCTGCAGC | 221178 |
rs201047372 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190404 | TAATAAGGCTGTAGT[A/T]ACCATGGATGGTGAT | 221178 |
rs201066975 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048681 | GTCTCTGATCAAAAT[A/T]AAAAAAAAGATAAAT | 221178 |
rs201070114 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024959 | AAATATATATATAAA[C/T]ATATATATAAACACA | 221178 |
rs201085395 | snp | C/G/T | | | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034825 | GAGCAGAAGCAAAAG[C/G/T]TCTCATCAGTCTTCT | 221178 |
rs201090720 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192186 | GGGCACAAAAGCAGC[G/T]TTGTAAACTCTTGTT | 221178 |
rs201091762 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046310 | TGCCTTTTTTTTTTT[A/T]AGAGTCAGAGTGTCG | 221178 |
rs201091898 | in-del | -/TCTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189470 | CAGAGCGAGACTCCA[-/TCTC]TCTCTCTCTCTATAT | 221178 |
rs201110509 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24094974 | AATTTGTAAAATGAT[G/T]TAGCCACTATGTAAA | 221178 |
rs201119748 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262326 | TTTTTTTTTTTTAGC[C/T]CTTTTGTGGTTGTTA | 221178 |
rs201127188 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043494 | TACACACACACACAC[A/C]CCCATGAACACACAC | 221178 |
rs201138891 | in-del | -/TATTCCCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095123 | TGTTCACAGCAGTGT[-/TATTCCCA]ACAGCCAAGAGGCGG | 221178 |
rs201150877 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993971 | GTGATGGTGGTGGTG[-/TTT]TTTTTTTTTTTTCTT | 221178 |
rs201154798 | in-del | -/C | 0.0225045 | 0.103662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033913 | ACAATCATCTTTTTA[-/C]TAAACAGAAAAGAAG | 221178 |
rs201165555 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24056908 | GGGAAATGGAACTTC[-/T]TTTTTTTTTTTTTTC | 221178 |
rs201167125 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112325 | GGTCAGTTTGCTACT[C/T]TGCTCTTGTTGCCCC | 221178 |
rs201168255 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262954 | CATACGTTCAGGTTA[-/T]TTTTAAAAAAAAAGA | 221178 |
rs201179342 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240986 | TATGATAGTTGCTTC[-/T]TTTTTTTGTTTTTTG | 221178 |
rs201219466 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202883 | ACTTACTTGCCCAAT[C/T]TAGGAGTGGAGAAGT | 221178 |
rs201231851 | snp | G/T | 0.0039921 | 0.0444985 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24278624 | TACAGGGTGCTTTCA[G/T]GTATCATCATTCCAC | 221178 |
rs201241170 | in-del | -/G | 0.0379877 | 0.132479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003170 | TGGTCTATAAATGCA[-/G]GGGTGTGTGTGTGTG | 221178 |
rs201272023 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24050557 | GGGACCCAGCTGGCA[A/T]GTGGCTGGAGCAGCA | 221178 |
rs201283210 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128737 | GTCCTACCTTATTTA[A/T]AAAAAAAAAAAAAAC | 221178 |
rs201291338 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24235654 | CCCAGCTACTTAGGA[A/T]GCCAAGGTGGGAGGA | 221178 |
rs201298811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100635 | TAGAAGGAGGAAGCT[A/G]TTTTCCAAAGGTCAC | 221178 |
rs201313667 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237987 | GCAATATATAAACAT[A/G]TATAATATATATATA | 221178 |
rs201331713 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090748 | TTGAACATATTTATA[A/T]TAGCTGACTTAAAAA | 221178 |
rs201340004 | snp | C/T | 1.78271e-05 | 0.0029855 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286180 | CCCGCCCACTCGTGC[C/T]CTATGCTGAGCGCAC | 221178 |
rs201345366 | snp | A/G | 0.0023012 | 0.0338424 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297761 | CTTGGCTCTGCAGGC[A/G]CCTGTGCCTCTGCTT | 221178 |
rs201357543 | in-del | -/CTTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142169 | TCTTATGTATCCTTC[-/CTTC]TCCCAGTGCCCCCCT | 221178 |
rs201361078 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191501 | ACTATACATTGCTTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs201378681 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228114 | CTTGTACTCTTTTTT[-/C]TTTTTTTTTTTTTTT | 221178 |
rs201394966 | in-del | -/TTA | 0.0901694 | 0.192235 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019075 | TAAGTTATATGATTC[-/TTA]TTATTATTATTATTA | 221178 |
rs201402934 | snp | C/T | 0.000116105 | 0.00761832 | missense | SPATA13 | GRCh38.p7 | 13:24251838 | GACCGTGTGGGACGC[C/T]GGCGGCAGATGAGAG | 221178 |
rs201406916 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041655 | GTGGGAAAATATCTA[-/T]TCAGAAAGTAGAAAA | 221178 |
rs201410278 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24050062 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACTGTGTG | 221178 |
rs201416950 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156120 | GTCACCTTGTGGCTG[G/T]GTGAATACTGCTGCT | 221178 |
rs201424215 | snp | A/G | 0.000379153 | 0.0137635 | missense | SPATA13 | GRCh38.p7 | 13:24294835 | GAGCATCGACAAGAT[A/G]GCTCGCTGGCAGGTG | 221178 |
rs201457951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254567 | TGCGACAGGATAGGG[A/G]CCTTCTAGAGGATCC | 221178 |
rs201467350 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201327 | AGAAAAACTACCCCC[-/T]CTCCCCTGTTCACTG | 221178 |
rs201468779 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112323 | TGGGTCAGTTTGCTA[C/G]TCTGCTCTTGTTGCC | 221178 |
rs201478500 | in-del | -/TG | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226533 | TCACTTTATAAACAC[-/TG]AGTAATATTACCTTA | 221178 |
rs201481847 | in-del | -/AT | 0.120674 | 0.21395 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237991 | ATATAAACATGTATA[-/AT]ATATATATATATAAA | 221178 |
rs201482584 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146932 | CTCATTCAGGCATGA[-/T]TTTTTTTTTCCTAGA | 221178 |
rs201491746 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148890 | CTGGTAGAGCGGCTT[G/T]TTTATTATTCATGGT | 221178 |
rs201500923 | in-del | -/ATATTATTATATAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190138 | AATAATATACAATAT[-/ATATTATTATATAA]CATATATATAATATA | 221178 |
rs201521111 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011760 | GAGAACATAGTCTTC[-/A]GCTCTGGCCAAGCAG | 221178 |
rs201527768 | in-del | -/C | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049498 | ACATCGCCTACATTT[-/C]TCAGAATGTAGCCCC | 221178 |
rs201532872 | in-del | -/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254028 | GGGAGGGCAGTTTGT[-/G]GGGGGGAAAGGAAGA | 221178 |
rs201534320 | in-del | -/TTG | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181342 | TTAGTTACTATAAGC[-/TTG]TTACTTTATAAATTT | 221178 |
rs201542293 | in-del | -/GGA | 0.0217236 | 0.101931 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253761 | AGGCAGAGATCCGAG[-/GGA]GGAGAAGTCCTAGCC | 221178 |
rs201542415 | in-del | -/AAA | 0.442791 | 0.15916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236596 | GGGAGACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 221178 |
rs201555751 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245584 | GAATTACAGTTGTTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs201566338 | snp | A/G | 0.00123874 | 0.0248563 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224426 | GTCCGCGAATTCAGA[A/G]GAAAGTGAAGGAAGG | 221178 |
rs201570891 | in-del | -/TA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064998 | CAGGCCACAGGAGCC[-/TA]AGGATAATGAAATGC | 221178 |
rs201590926 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202603 | ACTTTTTTTTTTTTT[A/C]TATTTGTAGATTTGG | 221178 |
rs201620960 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24257612 | TTTTTAAATTTTTAC[-/T]TTTTTTTTTTTTGGC | 221178 |
rs201628528 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181760 | GCTGTTTTACAGTTG[A/T]CTTTTTTTTTTTTTG | 221178 |
rs201633780 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139795 | CATGCAGGCCGGGCG[C/T]GGTGGCTCACGTCTG | 221178 |
rs201659176 | snp | A/C | 0.000331076 | 0.0128619 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249694 | ACGAGGACCCCCAGG[A/C]AAGCATGACTTCTGC | 221178 |
rs201659647 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269893 | TAATTTTTTTTTTTT[-/T]AGAGATAGGGTCTTG | 221178 |
rs201664859 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24238887 | ATTCTTGTATTCCTC[A/G]GTGAAAATAAAAAAG | 221178 |
rs201669597 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24051707 | GAGATGATATGAGGC[A/G]AATCTTCAGAGGTGG | 221178 |
rs201672406 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052503 | TATGTTTTTTTTTTT[C/T]TTTTAAACCCATGAT | 221178 |
rs201682620 | in-del | -/TT | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987738 | CCATCTGCAGAACTC[-/TT]TTTATTTTACACAAT | 221178 |
rs201686636 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291749 | GTCTTTATTTTTTTA[-/TT]TTTTTATTTTTTTTT | 221178 |
rs201693503 | snp | A/G | 1.78474e-05 | 0.0029872 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286178 | ATCCCGCCCACTCGT[A/G]CTCTATGCTGAGCGC | 221178 |
rs201695587 | snp | A/G | 0.00399195 | 0.0444976 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224339 | GCCCACCACACCCAA[A/G]CCCCAGAGCCCTCAG | 221178 |
rs201705213 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024496 | CAAGAAGAAAGGAGA[A/G]TGCTATCTGGAGTGT | 221178 |
rs201705687 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015748 | TGGCAGGCCCCCCCC[-/C]AATTCCTAGGTCCAC | 221178 |
rs201711908 | in-del | -/AAAAAAAAAA | 0.246769 | 0.249979 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999369 | TCCTCATTTTCTACC[-/AAAAAAAAAA]AAAAAAAAAAAGCCT | 221178 |
rs201727797 | in-del | -/AAA | 0.10653 | 0.204735 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128736 | AGTCCTACCTTATTT[-/AAA]AAAAAAAAAAAAACT | 221178 |
rs201774169 | in-del | -/CAAAAA | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303927 | AAACAAAAACAAAAA[-/CAAAAA]ACATTCAAACAACTG | 221178 |
rs201778361 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295697 | TCTCTCTCTCTCTCT[C/G]TCTGTATTCATAAAA | 221178 |
rs201816417 | snp | A/G/T | 0.000767723 | 0.0195786 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294915 | CCACTCGCCCTTCCC[A/G/T]CACCTTTGATCTGGT | 221178 |
rs201824372 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24194635 | TCCTCATTGATTCAC[C/T]ACTCACCGACTGGTC | 221178 |
rs201829120 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191756 | ACCTTGTGATCCGCC[A/C]GCCTCAGTCTCCCAA | 221178 |
rs201835049 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036038 | AAAAAAAAAAAGAAA[C/T]AAAGAAAAAACCTGA | 221178 |
rs201838486 | in-del | -/TTTC | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079669 | TGGGCTCTACTTTAT[-/TTTC]TTTCTTTCTTCTTTT | 221178 |
rs201841944 | in-del | -/TT | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139464 | AATTCTCCTCTGGGA[-/TT]GTATCACTGGCAGGT | 221178 |
rs201857953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989751 | TGCTGAAATCTAACC[C/T]CCAATGTGATGGTAT | 221178 |
rs201873486 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276658 | GAAGAAAGAAACAAT[A/G]AAATTTACTTTTTAA | 221178 |
rs201892125 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157298 | CTTTTTCTTTTTTTT[C/T]TTTTTAATATATTTT | 221178 |
rs201892388 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217892 | AACCCTCAAGTCACC[C/T]CCCACCACCACTGCC | 221178 |
rs201917131 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237138 | GAGGTGGGTGAATCA[-/CT]TGAGGTCAGGAGTTC | 221178 |
rs201923753 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064997 | CACAGGCCACAGGAG[A/C]CAGGATAATGAAATG | 221178 |
rs201924249 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048470 | ATCTAGTAAACTAAT[C/T]AAGGATGAAGAGGAT | 221178 |
rs201928977 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24163286 | ACTCACCTGTAGTCC[-/A]AGGTGCTCAGGAGGC | 221178 |
rs201935450 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015814 | GTGAGCCTCGGCTGG[C/T]GACACGTCATAGTCC | 221178 |
rs201962067 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030095 | ACACACACACATACA[C/T]ACATACATACATATA | 221178 |
rs201967066 | in-del | -/TA | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189621 | TTATATTTAATTTAT[-/TA]TATATAAATATATAT | 221178 |
rs201986006 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001494 | AAGGAGTGGCGGTGG[C/T]GAGGGGAGAATGAGC | 221178 |
rs201995023 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996416 | AATTGGGCAAAAAAC[-/T]GATCTGCAAATCAGT | 221178 |
rs202004588 | snp | A/G | 0.000264148 | 0.0114893 | missense | SPATA13 | GRCh38.p7 | 13:24286272 | ACCATGTGACCATGG[A/G]TGACCAGGAACTGGG | 221178 |
rs202006757 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025827 | CTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 221178 |
rs202018886 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204179 | ACCCGAATGCCTGTT[-/A]TGTGTTAGATACAGT | 221178 |
rs202032724 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208707 | CATAGGCCAAAAGAA[A/G]TCCCTGACAGTTCCA | 221178 |
rs202033547 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185880 | CCTGGCAAGTTCAAA[A/T]TAAGCAGGGTAGGTC | 221178 |
rs202042444 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278909 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 221178 |
rs202043368 | snp | C/T | | | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224070 | GGCGGGGCGGTCATG[C/T]ATGGGACCACTGCAA | 221178 |
rs202050011 | snp | C/T | 1.65419e-05 | 0.00287588 | synonymous-codon, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249686 | CCGTGTGGACGAGGA[C/T]CCCCAGGCAAGCATG | 221178 |
rs202056074 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201046 | TCACACACACACACA[C/G]ACACACACACACACA | 221178 |
rs202067356 | in-del | -/TGTGTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173363 | TCATTAGTTCTTAGT[-/TGTGTG]TGTGTGTGTGTGTGT | 221178 |
rs202068941 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074496 | TAGCACATTTAATTG[A/T]ACTCATGATGACTGT | 221178 |
rs202075804 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276651 | AAGAAAGGAAGAAAG[A/G]AACAATAAAATTTAC | 221178 |
rs202076330 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262465 | AGAATTCTTGATTCA[C/T]AGCCTAAGTGCATCA | 221178 |
rs202079240 | snp | C/G | 0.41325 | 0.18934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190185 | TATTATATAACATAT[C/G]ATATATAATATATAT | 221178 |
rs202081048 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302586 | TTCCATCTCTCTCCC[A/C/G]TCCCGAGTCAGGCTA | 221178 |
rs202087728 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046953 | GATTTGAGTAATAAA[G/T]TAATAAACTCCTGTT | 221178 |
rs202088156 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160782 | CCGCGATCGCCCTGC[A/G]GGTCGCTAGCTCCGA | 221178 |
rs202113391 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24213183 | AGGGTGATGAGAGCA[A/G]CTCAGAGATGATGAT | 221178 |
rs202116079 | in-del | -/AT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030094 | CACACACACACATAC[-/AT]ACATACATACATATA | 221178 |
rs202139177 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043683 | AGGGAATTTTTTTTT[-/G]TTGTTGACAGCCTTA | 221178 |
rs202155612 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170643 | AATTGGAACACCTGT[C/G]TCCTGAGATGAAGAT | 221178 |
rs202169312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023029 | TGTACCATGCTGGCC[C/T]GCTGCATCCTTCAAC | 221178 |
rs202175938 | in-del | -/GCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006755 | AGAGCACCGGGACAC[-/GCA]GCCCAAGCTCCTGGT | 221178 |
rs202193249 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138317 | CTGAAAAAAAAAAAA[-/C]AAAACAGTTTTACTG | 221178 |
rs202214256 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986321 | TTTAGATAACAAGAC[-/A]AGAGATCAGAATGGG | 221178 |
rs202228992 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119153 | ACCTTGTGATCTGCC[A/C/T]GCCTCGGCCTCCCAA | 221178 |
rs202233632 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221482 | GGAAAGGTTAAGGGG[-/T]GAGCAGGATTTTCAT | 221178 |
rs202234252 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182651 | CCTCCCCCAGGCCCC[A/G]CTTCAACACTGGGGA | 221178 |
rs202245045 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030066 | CACACACACACACAC[A/G]CACACACACACACAC | 221178 |
rs267603784 | snp | A/G | | | stop-gained | SPATA13 | GRCh38.p7 | 13:24286344 | ACAAGGACTGGTGGT[A/G]GGGCCGCAGTGAAGA | 221178 |
rs367576902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171025 | GCATGGAACACATTC[C/T]TCCATGCCCCTTCTT | 221178 |
rs367590556 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202347 | GCTAAACAGCCACAC[C/T]GAGTAGATGGCCCAG | 221178 |
rs367612503 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24241681 | CACCTCCCCGCGTGC[C/T]GGGATAATTCACCTC | 221178 |
rs367617406 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24244355 | TTCCTTTAGGTTAGG[A/C]CTCTGAATGGATATA | 221178 |
rs367622139 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063893 | TTATTCCAGGAGACC[C/T]CAGAGATGACTTCCT | 221178 |
rs367630987 | snp | A/C | 0.000115728 | 0.00760597 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286812 | CTCCAGCAGCACCCC[A/C]AGTGAGGAGCAGGAC | 221178 |
rs367639717 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030013 | GCAAAATTGAGTGGA[A/G]AGTAGAGTTCTCATA | 221178 |
rs367645501 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082452 | ATTGAGTTGCTCTTT[G/T]GAGAGTTTTGTCCAC | 221178 |
rs367646232 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042403 | GAAAGATCCATAGGC[C/T]GCTTTCTGAGATGTT | 221178 |
rs367658269 | snp | C/G/T | 3.31522e-05 | 0.00407127 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249665 | TGCAGACCCCCAGAA[C/G/T]GAAGACCGTGTGGAC | 221178 |
rs367663240 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063912 | AGATGACTTCCTTAA[C/T]GACCTGAGGTCTTCG | 221178 |
rs367670893 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24086312 | ATTTAGCTTTCACTG[G/T]GTGTCCTGTGCTTTA | 221178 |
rs367724093 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299234 | GGGGGCATCCTATGT[A/G]CTTTCAACAGTGTCT | 221178 |
rs367724935 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074145 | TTGAAGATCTGAAAC[-/CT]TGTCTTCATTAAACC | 221178 |
rs367727908 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027767 | TAACACCAGTATCAT[A/G]GCATAGTTGTGAAAA | 221178 |
rs367733309 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283027 | AGACCCTTCTGTGTG[A/C]CCCCGATCTTTGCAG | 221178 |
rs367743218 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127185 | GAGTTATTTACAAAG[A/G]TGTGGCCAGGGTAGG | 221178 |
rs367775443 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272256 | GGCCGAGGGAAGCCC[A/G]ACCCAGCCTCCAGCT | 221178 |
rs367783923 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117377 | ACCTAGTTATCCTTG[C/T]CTTTGCTAACCCATA | 221178 |
rs367789703 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173495 | CATACGCCTTTTATT[C/G]CCCCCCGTCCCCCAA | 221178 |
rs367797252 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24166477 | CGTAAACAGAGGTGA[A/G]GAGATGGGCTCCAGC | 221178 |
rs367818796 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084164 | TTATCTTCCGTAACT[C/T]AGCAACAAGCGAGAC | 221178 |
rs367852960 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098656 | GAAAGGGCCGGATGT[-/T]GGTGGTTTATGACTG | 221178 |
rs367853375 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999299 | CCTCCATTTTTTTCC[A/G]AGTCTGTTTTGGTCA | 221178 |
rs367857862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011475 | GTTGAGAGTGTCCCT[G/T]CTGGTGAGGACAGAA | 221178 |
rs367860080 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027170 | GACGGAGTCTAGCTC[A/G]GTCGTCCAGGCTGGA | 221178 |
rs367868680 | snp | C/T | 3.60972e-05 | 0.00424821 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297329 | CAGCTGTGGTAGAAT[C/T]GGAAGGTCTTAAGAT | 221178 |
rs367873281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207291 | TAATACCGAGGTGAT[A/G]GGATGATACGTGCAG | 221178 |
rs367878290 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151533 | ATACCCAGTTATATA[C/T]ATGAAAGTCCTGTCT | 221178 |
rs367878838 | snp | A/G | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979346 | AAGAAATTGTGAACA[A/G]GAATCCTGTATTTGC | 221178 |
rs367885827 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986401 | CGAGCCAAATTCCCA[A/G]AGATTTACATGTGTT | 221178 |
rs367888214 | snp | C/T | 5.01308e-05 | 0.00500628 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24284181 | CTTAGTGGATGACAA[C/T]GGTAGTGAGGAGGAC | 221178 |
rs367889412 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24111521 | CAAGTAATCCTCCCA[C/T]CTCAGCCTCCTGAGT | 221178 |
rs367898447 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083845 | TCCCGGCTGCTCCTT[C/T]CCTTGTCACTGGGGG | 221178 |
rs367904867 | snp | C/T | 0.000437904 | 0.0147905 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223991 | GAGACTTCAGGCACA[C/T]AGCCGGCTGCATGAC | 221178 |
rs367952929 | in-del | -/TTCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278930 | TCCTTCCTTCCCTCT[-/TTCC]TTCCTTCCTTCCTTC | 221178 |
rs367953334 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208337 | CTGTTAATTAGATGC[A/G]AAGTGGTTCCAATTC | 221178 |
rs367954434 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044038 | CTCTGAGCAGGAGGC[A/G]GTCAGGGAAAGTACT | 221178 |
rs367973035 | in-del | -/GAG/GAGG/GAGGG | 0.34101 | 0.232846 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108660 | CTGCTTTTCATGGTA[-/GAG/GAGG/GAGGG]GGGGGGGGGAAGCCT | 221178 |
rs367985564 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181925 | TTCGAGACCAGCCTG[A/G]TCAACATGGTGAAAC | 221178 |
rs367986400 | in-del | -/TGCCCAGAGTAGCCTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987079 | ACCCCATAGGCAGTG[-/TGCCCAGAGTAGCCTG]GATTGATATTTTAAA | 221178 |
rs368017216 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256172 | AACTTTTAAATAATA[A/G]TGAAAGTATATTTCT | 221178 |
rs368018485 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037771 | ATCGGAGTTTCTTAA[-/T]CTGGGGTTCGTGGAT | 221178 |
rs368026794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201682 | TTGAGCTCATGGTTC[A/G]CCCACCTTGGCCTCC | 221178 |
rs368047734 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983072 | TCAAGTGAAGTTGAT[C/T]GAAAACCAGCCACTG | 221178 |
rs368069113 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169706 | GTCTCTCTCCTCTCA[A/C]TCAAGCTCTCTGCAG | 221178 |
rs368083363 | in-del | -/TCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024456 | CATTCTCTTGGGTTG[-/TCTT]TCTAGTGACAAGACC | 221178 |
rs368085485 | in-del | -/ATATA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189693 | ATATTTATATATAAT[-/ATATA]ATATATTATATATAA | 221178 |
rs368100306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086283 | CATAGTCTTGCTAAA[A/G]AAAGGGATCTGAAAT | 221178 |
rs368114304 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24298907 | CATTGGCCTGGACTT[A/G]GGCCACTCCAAGATA | 221178 |
rs368124982 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229390 | AAGATCCCTGGCAAC[C/T]GGGGCAAACTGTTGA | 221178 |
rs368127756 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121097 | CTTAGATCAACTCTT[-/T]AAGAGTAGAACTTTA | 221178 |
rs368130996 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127522 | AGAAGGGTGAACCAT[A/C]GAGTGAACCAAGGAG | 221178 |
rs368169245 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997465 | CTTTTTACTTCATTC[A/G]GCATAATTTGAGATT | 221178 |
rs368175248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169155 | GCTGTCAGAACTTTG[A/G]TTTCCTGCCCTTCCT | 221178 |
rs368177517 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246645 | TGGGTGGATCATGAG[A/G]TCAGGAGTTCGAGAC | 221178 |
rs368195445 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037554 | CTGGGACTACAGGTG[C/T]GCACACCACCACACC | 221178 |
rs368217597 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23985081 | ATAACCAAACACAGA[A/T]GTGTAAAGAGTGAGG | 221178 |
rs368221759 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128056 | CTTCAAGGTGGGTGG[A/G]GAAGCTTTTTGCTTG | 221178 |
rs368226997 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196827 | TGAAGAAAATGGCCA[A/G]TTAATGGAGAGTAGT | 221178 |
rs368243464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168086 | GGACATTTTTCATGT[C/T]GACTTCATGAGCCTT | 221178 |
rs368255213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079154 | TCGGGGGAGGGCAGC[A/G]GGTGCCTAGGCCCTG | 221178 |
rs368258045 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24297934 | GATGTAGTTACTACC[A/G]GCAACATTTATTCAG | 221178 |
rs368267035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009576 | GTGGGATTGTTCCAG[A/G]TCATAGGTAGATTTT | 221178 |
rs368269440 | in-del | AT/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996416 | CAATTGGGCAAAAAA[AT/C]GATCTGCAAATCAGT | 221178 |
rs368273325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102898 | TGGAGACTTTTCCCT[A/G]TGTTTTCCTTCTAGG | 221178 |
rs368277895 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043644 | GTGAATCTGTCCCCA[A/G]ATTGTATGTCTCTCG | 221178 |
rs368282230 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189650 | ATATTTATATATATA[-/T]TATATATTATATATT | 221178 |
rs368297358 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24005881 | TTTTTCCCTTCTTAA[G/T]AAAGACATCCACCCC | 221178 |
rs368297515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063415 | TTCCTGTACTTATTG[A/G]GTTATCACAGTGCTT | 221178 |
rs368299819 | snp | C/T | 0.000115347 | 0.00759343 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24297635 | CAGTAGGACCACAGA[C/T]GAGGTTTATTTGTTT | 221178 |
rs368301246 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081715 | AAGCATAAATTTAAA[A/G]AAAATTAAAAATTGC | 221178 |
rs368302617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021860 | GGGACTACAGGCGCC[C/T]GCCACCACGCCTGAC | 221178 |
rs368368078 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057680 | TTACTTCCTGAAGAC[C/G]GGCAAGCCTGGCCTT | 221178 |
rs368379488 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189911 | ATATAATTATATTAC[A/G]TAATATATATTATAT | 221178 |
rs368395055 | snp | A/G | 0.000437904 | 0.0147905 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224251 | TCCAGGATGTGTTGA[A/G]CAAAGACTCCTGTGA | 221178 |
rs368397393 | snp | C/G | 0.000338811 | 0.0130112 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162404 | TGCTCCATCAGCATC[C/G]CTGGGTTCCTTGTGT | 221178 |
rs368398670 | in-del | -/GAGAGAGAGAGAAGA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103547 | GAGAGAGAGAGAAGA[-/GAGAGAGAGAGAAGA]AAATACATATGGTAA | 221178 |
rs368398938 | snp | A/G | 0.000680503 | 0.0184334 | intron-variant, nc-transcript-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24162431 | GTGTTCTTCCAGTCC[A/G]CCCTCTGTCACCTTG | 221178 |
rs368431742 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139666 | GAAACCCTCTCTGAG[A/C]TTGGTAAGTTAGGAA | 221178 |
rs368433839 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199057 | CCACTCTCAGCTAAT[C/T]TTTGTATTTTTTACA | 221178 |
rs368435178 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041323 | ATTTTACAGATAAAG[G/T]GTTTTTGTTTCTCTC | 221178 |
rs368439898 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136852 | ATTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 221178 |
rs368453868 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064991 | AACTGTCACAGGCCA[A/C]AGGAGCCAGGATAAT | 221178 |
rs368476038 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155014 | AGGTGTGTGCCACCA[C/T]GCCCAGCTGGTTTTT | 221178 |
rs368479159 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24093271 | TTTGAGTTCACTCAA[A/G]CTGTTCATCCTTCCT | 221178 |
rs368479250 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125309 | CCTTGACTTAGAGTA[A/G]GGAAACTTCCTGTCA | 221178 |
rs368489372 | in-del | -/ATTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110937 | TATTTTTTATTTTTT[-/ATTTTTT]GAGGTGGAGTCTTGC | 221178 |
rs368496229 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207300 | GGTGATAGGATGATA[-/C]GTGCAGCAAACCACC | 221178 |
rs368499226 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114905 | GACCTCTGGTGATCC[G/T]CCCACCTCGGCCTCC | 221178 |
rs368505669 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277215 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACAAGG | 221178 |
rs368516725 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188344 | CTCCAAAAAAAATAA[A/T]AAAAAAAAAAAGTGA | 221178 |
rs368546262 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077441 | TACACACGGACATAA[A/G]GATGGAAATAATAGA | 221178 |
rs368549603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067831 | TGCCTCAGCCTCCCA[A/G]ATAGCTGGGACTACA | 221178 |
rs368554553 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063210 | CCTGGTTTTATTCGC[A/G]TCTGCCTCCTCCTTG | 221178 |
rs368557566 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980898 | CGCCTGGCCAACAAA[G/T]TTTTTTAAAAAATAC | 221178 |
rs368594983 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210874 | CTCCTAATTCATGTT[C/T]ATAGGATATCTTTCC | 221178 |
rs368634421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170785 | TCTGGGTGTACTTTC[A/G]GATCCACTGAAAGAC | 221178 |
rs368636160 | in-del | -/TTA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054927 | AGCATTTAAACATTA[-/TTA]AGTCAATTTAGCTAG | 221178 |
rs368658748 | in-del | -/AC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23984845 | GATTGGTGCCAGCAC[-/AC]TTGGAGTTTGAAAAG | 221178 |
rs368660640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082274 | GTAAGTGTTCTGTGG[C/T]AGGGGCAGGCTTGAC | 221178 |
rs368668610 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197940 | CTTCTCAAAAACAGA[A/G]CTGTTGTTCTTCCAA | 221178 |
rs368675569 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190344 | TATTATATATAATAT[-/G]ATAATATTATATATT | 221178 |
rs368685363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013927 | AGGCCTTTCTGACTG[C/T]AGAGCCTGTTTTAAG | 221178 |
rs368686047 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139936 | AGCTGGACGTGGTGG[C/T]GGGCACCTGTAGTCC | 221178 |
rs368690683 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217167 | GGAGGATGAGGTGAG[A/C]GGATCACTTGAGTCT | 221178 |
rs368693359 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121720 | CTGTAGCCCTTGCCT[A/G]TTCTTTCCTCAGAAA | 221178 |
rs368696848 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275073 | GATGTCTTCTCTAAC[C/T]GTATTTGTAACAATC | 221178 |
rs368712885 | snp | C/T | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158766 | GTTTTAATTCTCCAC[C/T]CAATGCAGAGTGAGG | 221178 |
rs368713386 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126244 | TGCGGCTGTGACCCA[G/T]GATTGAGTCTGGGGG | 221178 |
rs368726451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037698 | CAGGCATGAGCCACC[A/G]TGCCCAGCCGGCTAA | 221178 |
rs368765487 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24039209 | AGTGCTAGAAACACT[A/G]TCTTGATTGTTCCAC | 221178 |
rs368800277 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24250373 | AGTACTGGTTTCTTA[A/G]TATAGTTTAGTAATT | 221178 |
rs368803372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234249 | ATATCATAATATATT[A/C]TTCAGTGTTTTCTTA | 221178 |
rs368804782 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015813 | GGTGAGCCTCGGCTG[C/G]TGACACGTCATAGTC | 221178 |
rs368805709 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154693 | GGTGAGGAGTCTGGG[C/G]ACAGCTTAGCTGGCT | 221178 |
rs368806240 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24203685 | TTCAATTCTCAAACT[C/T]GTTTCTCTTTTTTGT | 221178 |
rs368807059 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189733 | TATATAATATATAAT[A/G]TATTATATATAAAAG | 221178 |
rs368843252 | snp | C/G | 1.69433e-05 | 0.00291056 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284097 | AAAATCTTGTTAGCT[C/G]TGTCTTTTAAATCAT | 221178 |
rs368845953 | in-del | G/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24199019 | AGTGGTTCATTCTTT[G/TT]TTCTCTTTTCAGGCA | 221178 |
rs368857210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168354 | TGTGAATTCATGTCT[C/T]GAGTTTATGATTTGC | 221178 |
rs368860812 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24289675 | TGAAGGCAGACCCGG[A/G]CATGCGGCTCCAGGA | 221178 |
rs368871533 | in-del | -/AGT | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291883 | TGCCTCAGCCTCCCG[-/AGT]AGCTGGGACTACAGG | 221178 |
rs368878044 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245609 | TTTTTTTTTTTTTTT[A/T]GACAACAGGTCTTGC | 221178 |
rs368880875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009531 | GTACATTGGTTTGGT[C/T]TGGAAAGATGGGACA | 221178 |
rs368889322 | snp | A/G | 4.94279e-05 | 0.00497107 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290729 | CGCCAACCTCATGAA[A/G]CAGGGCAAGTACAGA | 221178 |
rs368898309 | snp | A/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159469 | AAAACAGGAATGGAA[A/G]GTACACGGAGTTCTG | 221178 |
rs368911490 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105944 | GAAACCAAGCCTGCT[G/T]ACACCTTAATCTTGA | 221178 |
rs368934922 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199021 | GGTTCATTCTTTTTT[-/T]CTCTTTTCAGGCACA | 221178 |
rs368953518 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292307 | CAGCCCAGCTGTTGG[A/G]TACCTCAAGGTAGCA | 221178 |
rs368961988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006195 | GGAGGGTATAGAGGG[G/T]AAGTCTAAATGTCAG | 221178 |
rs368963131 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24165587 | GTTGCACCCCCCACC[C/G]ACCCCAACTCCAACT | 221178 |
rs368966052 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292635 | AAATATCTTCCTGCA[G/T]GGAGTGGAGAGTGAA | 221178 |
rs368972967 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010734 | CCTCCCTCCTGCTCC[A/T]CCATGGGGCAATTCA | 221178 |
rs368980655 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24229882 | AGATACACTTAAAAC[A/G]TAGGAGAACTTGATG | 221178 |
rs368980833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032321 | TGGCAATACCACATA[A/G]CAGTGGTCCCTATAC | 221178 |
rs368989858 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090489 | CCCTCACCGAACGGT[A/G]TCCTCACCTGAGCTT | 221178 |
rs368993153 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064259 | AGAATGGCTACAGTC[A/T]CCGTTTCGTCAAGCC | 221178 |
rs368994523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101510 | AACAACACATAAAAC[G/T]TACCACCTTAACCAT | 221178 |
rs369004047 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019129 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 221178 |
rs369013916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273986 | TGAGCCACTGCGCCC[A/G]GCCAATGGTTAAACT | 221178 |
rs369021870 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170641 | GAATTGGAACACCTG[-/GT]TCTCCTGAGATGAAG | 221178 |
rs369030839 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993026 | TCTGGGCATCATATT[A/G]TGTGCCTGGGCTCGG | 221178 |
rs369038043 | snp | A/T | 0.000190476 | 0.00975714 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223120 | ACACGGACACCCAGG[A/T]AGCCAAACTCAGCCC | 221178 |
rs369040656 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198103 | CGGATTCAAGCGATT[A/C]TCCTGCCTCAGCCTC | 221178 |
rs369059508 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081479 | TAAACTCACATCAAT[A/G]GTATGAGGCTGTAGG | 221178 |
rs369071741 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095911 | TTCCTTTATCACACC[C/T]AGGTTCCTTCAGACG | 221178 |
rs369080025 | in-del | -/CAGTTTGAACA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074936 | TGCCTTATTTGAACA[-/CAGTTTGAACA]GTTGGCTGCCTGTGA | 221178 |
rs369111933 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980632 | CAGTCTTACTTTGTC[G/T]CCCAGGTTGGAGGGC | 221178 |
rs369112878 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160633 | AGGGAGTGAGCTAAC[C/T]GGGGGCGTGGCCTGA | 221178 |
rs369115177 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157473 | CGGCTAATTTTTTTT[-/T]GTATTTTTAGTAGAG | 221178 |
rs369116708 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012505 | GGAGTGGGAGAGGAC[A/G]AGCATATGGCAATTT | 221178 |
rs369119596 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24032075 | GTAAGTCAGTTTAGT[A/G]AGAACACCCATGCTT | 221178 |
rs369124141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177338 | TAAATTTATTTCTTA[C/T]AGCTCTGGAGGCTAG | 221178 |
rs369126946 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022478 | ACTTTAAAATTTTAA[A/T]GTAATGTTTAATGAG | 221178 |
rs369136913 | snp | C/T | 5.31844e-05 | 0.00515649 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286191 | GTGCTCTATGCTGAG[C/T]GCACCCCACTGTCTC | 221178 |
rs369139559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198277 | AGATTACAGGCGTGA[A/G]CCACCGCACCGAGCC | 221178 |
rs369157888 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188980 | TCTGGATATTTTTAG[C/T]CCACTGTTGAGACCT | 221178 |
rs369160621 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24066681 | GTCTGTTTTCACCCC[-/C]TCAGGCCCCCCACCT | 221178 |
rs369161699 | in-del | -/AC | 0.496245 | 0.0431677 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138319 | GAAAAAAAAAAAAAA[-/AC]AACAGTTTTACTGAA | 221178 |
rs369177026 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979769 | AGGTCCCGCCCTGGC[C/G]GAGGAAATGAAGAGG | 221178 |
rs369188011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021320 | AAGCATAGCTTGCAT[A/G]AAGATGATTAAGAGA | 221178 |
rs369199433 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292787 | TGGATCACATGAGGT[C/T]AGGAGTTTGAGACCA | 221178 |
rs369202682 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164085 | AACACCAAATGTACA[C/T]GGTTTTCTTGAGGGA | 221178 |
rs369237405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085441 | TTCTGCCTGCTTTTT[A/G]ATAAGCAACATTGGC | 221178 |
rs369255726 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186890 | ATTGGTGAATTTATT[A/G]AGAAGTTGATTTCAT | 221178 |
rs369255862 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171994 | CCGAATGATGACATC[C/T]TGCAAGACTGTACTA | 221178 |
rs369275269 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260755 | CTCTGGTTTTATTGC[A/T]CAACGTTAAAGAAGC | 221178 |
rs369287981 | in-del | -/TATAT | 0.339882 | 0.233284 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189843 | TAAAATGATATTTAA[-/TATAT]TATATTAATATATCA | 221178 |
rs369292654 | in-del | -/G/TTTG | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122647 | GCACATACTGTATAT[-/G/TTTG]CACTTCAAGATACTT | 221178 |
rs369298389 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992702 | CTGAGCTTGAAAGGG[A/G]CCCTGCAGGAGAGGG | 221178 |
rs369354522 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036570 | CCCTGCCACCTGGGG[C/T]CCACAGGGAGACACC | 221178 |
rs369363325 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109946 | CACATTGCCAAATTG[A/C]CTTACAGAAAGTTTG | 221178 |
rs369365157 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987681 | GTGTGCAGTTCAGCG[G/T]CATTCAGCACATTCA | 221178 |
rs369367554 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987105 | TTAAATGAACTAGAG[G/T]ATTGAAACCTACACT | 221178 |
rs369378402 | snp | A/G | 0.00046561 | 0.0152508 | missense | SPATA13 | GRCh38.p7 | 13:24302607 | AGTCAGGCTACAACA[A/G]GTGCCCTGTGGCCCC | 221178 |
rs369392629 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138126 | CCAACATGGTGAAAC[C/T]CCATCTCTTCTAAAA | 221178 |
rs369404921 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24180337 | TGAACCTTTAGTTCT[A/G]TTTTCATTGATCTAT | 221178 |
rs369419486 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220665 | CCCCCTAATTCCTCC[A/G]TTAGAACATTAAACT | 221178 |
rs369425378 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239793 | ATTAAGTTCTCCTCA[A/G]TCAATAAGTTTAATT | 221178 |
rs369425935 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113899 | AAAAAAAGAAAGAAA[A/G]AAAATATAGTTATAT | 221178 |
rs369432902 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24152782 | CAGAGACAAAATGCA[C/G]AGCCACTCCAAGTCC | 221178 |
rs369460548 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044623 | TTTAATGATCGAATC[A/G]GGGTAATTAGCATAT | 221178 |
rs369464702 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230461 | GGGTCTTTAGTGCCC[C/T]GGGCGGCGGTTGCAG | 221178 |
rs369474673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163553 | ATATCCATTTCATTA[C/T]GTAATCTTAAAGCCT | 221178 |
rs369497864 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24129253 | AGAGGAGCAGCCAAC[A/C]ATCAAAGTCTGAGTA | 221178 |
rs369498422 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189902 | ATATATATTATATAA[-/T]TATATTACATAATAT | 221178 |
rs369499737 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077814 | CCTCTTGCTGTCCAA[C/T]CCCATGGCTTGAAAC | 221178 |
rs369528351 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211593 | GTAAGGTGCATCTCC[A/G]TTGGACCCAGCCTGA | 221178 |
rs369529565 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224896 | AAAATAAGTTGTAAA[C/T]AAACTGTCTTCTGCT | 221178 |
rs369550533 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044886 | GGTGGTTTCCAGAGG[A/T]GGGGGTGGGGGTGGG | 221178 |
rs369574245 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192820 | GACATGGGAAAAAAA[A/G]GCCTTCTGCATGGGT | 221178 |
rs369600023 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295872 | ACTGAAGCACAGAAA[A/G]GTTAAATAACTTGCC | 221178 |
rs369603488 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287041 | TCCACCCCCCGCCCC[A/C/G]CCATCAGGCTCCCAC | 221178 |
rs369609973 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038285 | CAATATCTGCTATAA[G/T]GGGATCAGAAAAGGC | 221178 |
rs369612264 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269161 | CTGCAATATGTTCTC[A/G/T]AGTAATTCTGTGAGG | 221178 |
rs369619205 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24002770 | GAAACAGGTTTCCTA[A/C]CCGCTGCTGCTCTGC | 221178 |
rs369632250 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24235942 | TCAGTGGATGAAGTT[C/T]CATCATGCAACACTG | 221178 |
rs369646493 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248380 | CTGAGATTGCACTAG[C/G]TCTTGGGCCAGACAC | 221178 |
rs369654431 | in-del | -/TTTTTCTTT | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157284 | CAGTCAGGTAACTCC[-/TTTTTCTTT]TTTTTCTTTTTAATA | 221178 |
rs369692310 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24199285 | GCCGCTGAGCTCTTC[A/G]GAAGGTGGGAAGCTG | 221178 |
rs369694227 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164181 | GGAGAGAAATGCATT[A/G]GTACAAAGTGCTTAC | 221178 |
rs369701127 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115477 | AACCCTATTGCAAAC[C/T]GCGCATGCGAAGGAT | 221178 |
rs369707928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251636 | GTGAGTGGCTTCGAG[A/G]TGAGAGCGCTATGCG | 221178 |
rs369711697 | snp | A/C/G | 0.00227767 | 0.0336721 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223031 | CCCCTGTGCAGGCTC[A/C/G]GACCTGAAAGACGCC | 221178 |
rs369723306 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206873 | CTCCAGCCTGGGCAA[-/C]GAGTGAAACTCTGTC | 221178 |
rs369731972 | in-del | -/TCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24079679 | TTTATTTTCTTTCTT[-/TCTT]CTTTTTTATCTAAAA | 221178 |
rs369737629 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011700 | CTCTACTAGTTAAGC[-/A]GGAGCCTGGGAGTCT | 221178 |
rs369746647 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996193 | CAAAGTGGGCTTCAC[C/T]GGGCTGACTCAAGGA | 221178 |
rs369753547 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082737 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAAGCG | 221178 |
rs369756494 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122081 | CAATTCATCCCTGGT[-/G]CTGGGCCTCCAAAAT | 221178 |
rs369779751 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087542 | AGGCACCTATGCAGG[G/T]GAAAATCTTTGGATT | 221178 |
rs369784550 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027784 | CATAGTTGTGAAAAC[C/T]GAGGAAATTAGTATA | 221178 |
rs369807935 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016052 | GCCACAGTGACACGT[A/G]GCATGGTTCTGAGCT | 221178 |
rs369813488 | in-del | -/CAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144098 | TGTGCACTAACTCAG[-/CAG]TGGCCCCAGTGGGAT | 221178 |
rs369840337 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138026 | TTTTACTGGGCCAGG[A/C]GTAGTGGCTCGCGCA | 221178 |
rs369841721 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24152545 | CACAGCGGGTGTTCT[A/G]TGCCAGTGAGGGAAT | 221178 |
rs369855151 | snp | C/G | 2.06111e-05 | 0.00321016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300502 | AGAAGGCTTTGTCCC[C/G]TTAATGCTTATCAGT | 221178 |
rs369869581 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121635 | GACAGAAATTGGACA[A/G]ATGCTCATAGGTGTA | 221178 |
rs369870505 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207378 | ACCCCTGAACTTAAA[A/G]TAAAAATCGGAAAGA | 221178 |
rs369880147 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282567 | TGGATCTCAGTTCCT[A/G]ATGCCATTTCCTCGG | 221178 |
rs369886708 | in-del | -/AACCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052080 | TGGCTTCTTACACCA[-/AACCT]GCATCCTGTGCTGTG | 221178 |
rs369886732 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24099757 | CCAGATTCAGGGAAT[C/G]TGCAGATCACATGGT | 221178 |
rs369890695 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127159 | GATGACTAGAGGACT[C/G]TTTAATAAGGGAGTT | 221178 |
rs369892603 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24137825 | GTGCTCTTTGACTAT[C/T]TTATGTGCGTCATCA | 221178 |
rs369897389 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127373 | GGAGTTGACAACCAG[C/T]GTCATTTCCTTCTCT | 221178 |
rs369929597 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123964 | GGCAGACTCTGGCCA[C/T]GGGAAAGGAAGGCTC | 221178 |
rs369953654 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24129623 | AGGGCCACCCTATGT[A/G]TGGAATCAAAGGAAG | 221178 |
rs369959878 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983286 | ACTGCCTTCTTACTG[C/T]GTCTTCACGTGGTCA | 221178 |
rs369961874 | in-del | -/GCATATATGAATATTA | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065546 | ATTCAAGACAGCGTG[-/GCATATATGAATATTA]GCAAGTAACATGGAA | 221178 |
rs369963303 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090718 | AATTCTTTAGACATG[A/G]CCTCCTCCAGTGATT | 221178 |
rs369976660 | snp | C/T | 0.0024616 | 0.0349963 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251693 | TTCCTGGTACCTCCT[C/T]ACAGATTTTGCTTTC | 221178 |
rs369980613 | snp | C/T | 0.000437968 | 0.0147916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289182 | TTTCTTCAAAATGTG[C/T]GTCACCCTTTACTTC | 221178 |
rs369983736 | snp | C/T | 6.95858e-05 | 0.00589814 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297356 | AGATGTGTTTTCATC[C/T]TTCCAGGGACTGGAT | 221178 |
rs369986600 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190100 | ACATATAATGATATA[C/T]AATATATATTATTAT | 221178 |
rs369989225 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121885 | ATCCCCCAAAATCCC[A/G/T]CTGGTTTCTTTTCCA | 221178 |
rs369991189 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24225230 | GGGTGTGTGAGTGAG[C/T]GAGCATGGAGTCCAG | 221178 |
rs369995276 | in-del | -/TGTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105132 | TGTTTTGTTTTGTTT[-/TGTTT]CTGTGAGACAGAGTT | 221178 |
rs370020294 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198214 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG | 221178 |
rs370024799 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199740 | TTTTCAATAGGCGCA[A/T]AACAGTGTCAGATCA | 221178 |
rs370028431 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218929 | TTTATTTAAAAATTA[C/G]TGGTCAGAAGCTTTT | 221178 |
rs370037430 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24097832 | CTGTACAATCCAAAC[A/G]CAGGCGAGGGCCCCA | 221178 |
rs370038372 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24031360 | CTAGCACACCAATTC[A/G]TGCTAGCACATCTCC | 221178 |
rs370042920 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134816 | CAGAATGTGTCCCCC[A/T]AAATTTTGCATGTTG | 221178 |
rs370053496 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127231 | AGCTTACCCAGGCTG[A/G]TAGCAGTGAGGCCAC | 221178 |
rs370061177 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304575 | CTCCCCTGCAGCCCC[C/T]CACATCCAGAGCCGT | 221178 |
rs370067509 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185816 | ACACATACATCAAGA[C/G]ACAGAGAGAGAGAGA | 221178 |
rs370105491 | in-del | -/TAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190349 | ATATATAATATATAA[-/TAT]TATATATTATTATAT | 221178 |
rs370126251 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24080136 | GTCTTTTATCTAAAA[C/G]AGGCAAATCTAAATC | 221178 |
rs370127380 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161399 | GACCCGGAGCGATGC[G/T]GTTGGAGAGCTTAGT | 221178 |
rs370136008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290458 | AAGCACCCCTTCTCG[C/T]CGGCCAGATAACGCT | 221178 |
rs370146559 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189717 | ATTATATATAAAAGC[A/T]TATATAATATATAAT | 221178 |
rs370147420 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260092 | CCTACAGAGCTGCCA[C/G]TGTGGTGGATGAATG | 221178 |
rs370148919 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204655 | ACTTTCTTTCTCTAC[A/C]AATTTGACTTCTCTA | 221178 |
rs370151399 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24236071 | CATAAGTAGTGAGGG[G/T]TGGGGTCGGGCCTGC | 221178 |
rs370156150 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23984388 | GGAGAGTAGTCTTCT[A/G]TTTTATCCATCATTT | 221178 |
rs370165292 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277368 | AGAATGGCGTGAACC[C/T]AGGAGGCGGAGCTTG | 221178 |
rs370193328 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142469 | TCTCCCCCCTCAGTT[C/T]TGGATTGTCTGATGT | 221178 |
rs370210362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982900 | CTGGAGTGCTAGGTG[C/T]AAGATCCCTTCTCTC | 221178 |
rs370212716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273313 | AGGGTGCAGGGCCCT[A/G]AGTTGAATACTGATG | 221178 |
rs370222674 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211663 | CCAGCTGGTCAGCAG[A/G]CCATGTTGACTCTCT | 221178 |
rs370230669 | in-del | -/AC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190237 | AATATATATTATTAT[-/AC]ATAACATATCATATA | 221178 |
rs370233739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268550 | GACCACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 221178 |
rs370244416 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269831 | TGGGCTCAATTGATC[C/T]TCCCACCTTGGCCTC | 221178 |
rs370247251 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24091520 | AGCTCTAAGAATTGA[A/G]CTTTTCAGGCTGGAT | 221178 |
rs370262806 | snp | A/C | 0.000215146 | 0.0103695 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223952 | TCCTAGGAGTGGGGC[A/C]CCATCCCCTGGAGAG | 221178 |
rs370299897 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146817 | TACGGAATATCCTAT[C/G]TCCCAGATGGACTGA | 221178 |
rs370301685 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270144 | GAAGGAAGCTCACTC[C/T]TTGTTAACAGTCATT | 221178 |
rs370302813 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001345 | GTGTCTCGTGGGAAG[G/T]CTGCAGGAGTGGAGG | 221178 |
rs370307577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198272 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGCACC | 221178 |
rs370318202 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232371 | CAAGTCTTCTTTACT[C/T]TACTGATTACTGATT | 221178 |
rs370319037 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24020692 | TCAGTTAAATTCAAT[A/G]AATACTTTTTAGTAC | 221178 |
rs370319141 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24050827 | CGTGTGGTAGTGGCA[-/G]GTCATTTGTGTAACA | 221178 |
rs370321111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028595 | CTAGGAGAGATCTGG[C/T]ATTATATTCTTTATG | 221178 |
rs370337556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274426 | TTCTAAACATTTTCC[A/G]TGTGATTAGATGCCA | 221178 |
rs370340032 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23988547 | TTTGCTGAGAAGAAC[A/G]TTTTGGGCACATTAA | 221178 |
rs370342089 | in-del | -/GGTGAACCATCG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127523 | AAGGGTGAACCATAG[-/GGTGAACCATCG]AGTGAACCAAGGAGA | 221178 |
rs370362895 | snp | C/T | 0.000153988 | 0.00877328 | stop-gained | SPATA13 | GRCh38.p7 | 13:24251802 | CCCTTCACATTCTCC[C/T]AGAGCACCCCCATTG | 221178 |
rs370372766 | snp | A/G | 9.19008e-05 | 0.00677805 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286423 | CTTGCAGCTTTTCCA[A/G]AGTACCTGGGGGAGC | 221178 |
rs370376387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232218 | GTAAGTCATGGAGTC[C/T]GAAGGCCCAAGAACC | 221178 |
rs370389275 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026891 | ACAGGCGTGAGCCAC[C/T]ACACCTGGCCAACTG | 221178 |
rs370391575 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24225803 | ACTGTCTGTAGCTCG[A/G]TGAGCTGGCCAGGAA | 221178 |
rs370393998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077334 | ATGGCTCCTGTAACT[A/G]TAGTTAACCTCTACT | 221178 |
rs370396632 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304653 | GGTGAACCCTTGGAA[C/T]ATTCTGTGACCGCCT | 221178 |
rs370414193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255303 | TCTGCTCCATCAAGA[A/G]GCCTGAGTCTGGGAG | 221178 |
rs370416724 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262305 | TTAAAACAAAGTTTT[C/T]TTTCTTTTTTTTTTT | 221178 |
rs370418510 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996679 | GATGTTTACACATCA[A/G]TGAGGTTACAGTTCA | 221178 |
rs370423871 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980790 | AGAGAAAGGGTTTCA[C/T]CATAATGGCCAGGCT | 221178 |
rs370468360 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24251819 | GAGCACCCCCATTGG[G/T]TTGGACCGTGTGGGA | 221178 |
rs370485930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176868 | TCCTGGGTTCAAGGG[C/T]TTCTTGTGCCTCAGC | 221178 |
rs370491106 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065146 | GATGTTTACCTGTCA[A/G]GGGGATGTCTAATAA | 221178 |
rs370493959 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291756 | TTTTTTTATTTTTTT[-/A]TTTTTTTTTTTGAGA | 221178 |
rs370504252 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124621 | ATGGCATTCTACCTC[G/T]TCAAAAGCTAAACAG | 221178 |
rs370507157 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24028856 | AAAGATTTGTGTTTT[C/T]TATGTTTCTGGTCAT | 221178 |
rs370511784 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185724 | ATACAAATAGATGCA[G/T]TTTTTTTTTTTCATG | 221178 |
rs370515360 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088959 | CTGGAGACAGGGATG[A/C/T]GGTCATCGACAGCTC | 221178 |
rs370517112 | in-del | -/TAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190107 | ATGATATACAATATA[-/TAT]TATTATATAACATAA | 221178 |
rs370526129 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134084 | GCAAATGGTCCAAAC[A/G]GAGTGACAAGGTAGA | 221178 |
rs370539930 | in-del | -/T | 0.0532146 | 0.154193 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052867 | CTGCCCACCACATTA[-/T]TTATACTACATGTCT | 221178 |
rs370579972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028826 | TTCATTTCAATAATT[A/T]TATTTCTCTATTTTA | 221178 |
rs370583983 | in-del | CCTGCATGTGTGCACATGCGCGTGTGC/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114390 | GCACATGCGCGTGTG[CCTGCATGTGTGCACATGCGCGTGTGC/T]GTGCATGTGTGCACA | 221178 |
rs370596770 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057802 | AGGTACAGAGCCCAG[C/T]CTTCCCCTTGGAGGT | 221178 |
rs370605047 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070755 | GAACGGAAGGCTGAC[C/T]CTCCCCCAAGTAATG | 221178 |
rs370612593 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189660 | ATATATTATATATTA[C/T]ATATTTATATATTAT | 221178 |
rs370616466 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190347 | TATATATAATATATA[-/T]ATATTATATATTATT | 221178 |
rs370623978 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278494 | TGTTGCCCAGCTTGG[A/T]CCCAAACTCCTGGGC | 221178 |
rs370637722 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24120191 | TTGGGATTCTGTTTC[C/G]GCCTCTGAAAAAAAA | 221178 |
rs370640785 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285853 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 221178 |
rs370649742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097175 | ACCCGGCATGGGTGG[C/T]TGGGTGGGTGTGTGA | 221178 |
rs370659930 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207561 | CAGTACACCCGGGTT[A/C]GTTTCTCCACATCCC | 221178 |
rs370672628 | in-del | -/AC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24167671 | CCCAAGTGCCAGTTT[-/AC]ACACACACACACTCA | 221178 |
rs370706754 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139928 | AAAACATTAGCTGGA[C/T]GTGGTGGCGGGCACC | 221178 |
rs370713769 | snp | C/G/T | 0.00557734 | 0.0525397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240824 | ATCTTTTATCATCCA[C/G/T]GTAACACATTCAAGG | 221178 |
rs370723052 | snp | C/T | | | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035355 | AGACAGGTTTTGCCA[C/T]GTGGGCCAGGCTGGT | 221178 |
rs370727012 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980255 | GCGCATAGGGGCGCC[G/T]GGGCAGTAGTTGCAC | 221178 |
rs370732242 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24265253 | GCCCAACAGGAGTCG[G/T]CCTGCTGAGGCAGCA | 221178 |
rs370739931 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037555 | TGGGACTACAGGTGT[A/G]CACACCACCACACCT | 221178 |
rs370740613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285219 | CTTTTTAATTGTTAA[C/T]GATCTCAAGATCATG | 221178 |
rs370749413 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271027 | CTCTCTCTCACTCTC[A/T]CTCTCTCTCTCTCAC | 221178 |
rs370749526 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24259159 | CTGCAGGAATGCTGC[C/T]ACCTCCTTGCTAAGC | 221178 |
rs370757460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003411 | AATAATGAATGGAGT[A/G]CACACAGGAAAGGGT | 221178 |
rs370779163 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217320 | TCTCTTTTTATTACA[A/G]TTCTTCTTCCTAATA | 221178 |
rs370780327 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157366 | TGCAGGGGCGCGATC[G/T]CGGCTCACTGCAAGC | 221178 |
rs370798059 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172990 | TTCATCAGCATTGTA[C/T]GGCTTTCAGCACACA | 221178 |
rs370804253 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187861 | AATTAATAACTCTAC[A/G]ATAACCTCTAAGTGT | 221178 |
rs370807640 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303892 | GCCTGGGAGATACAG[C/T]GAGACTGTCTCCAAA | 221178 |
rs370810666 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025199 | CTATTTTTGTTTATT[A/T]CCTAAAATTTTTATT | 221178 |
rs370812853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277248 | AGGAGATCGAGACCA[C/T]CCTGGCTAACATGGT | 221178 |
rs370828417 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986455 | TAGTTTTTAAGGTCC[-/C]TTCTGCTCCTTCTAA | 221178 |
rs370842895 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195559 | GCCCCATTTTACAGC[C/G]CACCAGCAATATAAG | 221178 |
rs370856332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211910 | GGCATTAGAGCATCC[A/G]TGTGTCGGCTGAAGG | 221178 |
rs370867787 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232768 | TCCCCAGGCTGGTCT[C/T]GAGCTCCTGAGCTCA | 221178 |
rs370885015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292919 | GAAAATCGCTTGAAC[C/T]CAGGAGGCGGAGGTT | 221178 |
rs370890759 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124527 | CTGGTGGGACGCAGT[G/T]CTCTCATCTAGATTC | 221178 |
rs370903619 | in-del | -/GTTTT | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980589 | CTCCTACTTAACGAA[-/GTTTT]GTTTTGTTTTGTTCG | 221178 |
rs370904835 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263523 | GGCTGTGCAAAAGTC[C/G/T]CTGATATAAAATGGC | 221178 |
rs370937011 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24060259 | AGTGGAACAGAATAG[A/G]GAGCCCAGAAATACT | 221178 |
rs370960870 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110167 | GCTTTCCAGAGGAAG[C/T]GGGAGCAGTAAAAAC | 221178 |
rs370973016 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293771 | CTGGGTGTGAATGGG[C/T]GTCTCTGAAGACAGC | 221178 |
rs371009446 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054922 | TGTCCCAGCATTTAA[A/T]CATTAAGTCAATTTA | 221178 |
rs371010743 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116388 | GCCATCCTCCAAGAC[A/G/T]GGAGACACAGAATTG | 221178 |
rs371041792 | snp | C/T | 0.000148332 | 0.0086107 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290795 | GATTGACATCGCCAT[C/T]GACGGGTTCCTGCTC | 221178 |
rs371045285 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210781 | GTTTTTTTTTTTTTT[G/T]TATTTCATTGGAATT | 221178 |
rs371052420 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125418 | AAGCAAAGGCAGGAA[C/T]CAGGGGGCATGGAGG | 221178 |
rs371058430 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150678 | CAGAATCCACAGGGC[A/C]AGGCAGGCCACAGCA | 221178 |
rs371062596 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201459 | GTTCACTCTTTTTTT[G/T]GAGACAGAGGCTTGC | 221178 |
rs371067960 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083611 | CAGAGAATAATATTA[C/T]AGGTGTTGGGAGAGC | 221178 |
rs371076193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088524 | ATCGTTGGGTCCACA[A/G]CCCAAAGACTGGCAG | 221178 |
rs371082993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187629 | ACATTTCAAGCATTT[A/G]AATTATTATATCTGT | 221178 |
rs371088439 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237562 | GAGAGTATTTAATGG[A/G]TTCAGAGATACATTT | 221178 |
rs371089716 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104411 | TACAATTCTCAAGGC[A/G]GGCATAAATCCGCTA | 221178 |
rs371101434 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046557 | GGTGTGTACTCTTTT[G/T]TGTCTGGCCTCTTTC | 221178 |
rs371110092 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117692 | ATTAAGAGAAAAAAA[A/C]CCCCAAACTCATTCC | 221178 |
rs371123785 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992808 | ACGTTTGGCTCCACA[A/G]TGCTGGGAAACACTG | 221178 |
rs371133023 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24039739 | CAATCCTGCATGTGA[A/C]TGGGGTTGGGGGAAT | 221178 |
rs371134227 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24009277 | CTGTGAACCAAAAGT[A/G]TCTGAGATACGTCTC | 221178 |
rs371138842 | in-del | -/GGGAGT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217757 | GCTTGAGCTGGGAGT[-/GGGAGT]TGGTGCTGCCCACAG | 221178 |
rs371141464 | snp | C/G | | | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162167 | TTCTCATCTACCTCC[C/G]TTGGCCCCCACGTTT | 221178 |
rs371145532 | snp | A/C/G | 3.66369e-05 | 0.00427988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286714 | TCCTGCCTCTGCTCC[A/C/G]TGCTGCCCTCCCCTG | 221178 |
rs371145803 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24179514 | CAGTGTACAGTTCAG[C/G]CATAGTAAGTACATT | 221178 |
rs371148808 | snp | C/G | 7.28505e-05 | 0.00603489 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286724 | GCTCCATGCTGCCCT[C/G]CCCTGCCCCAAGTCA | 221178 |
rs371151629 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23984508 | ATGGCCCCGCGCAGC[A/C]CCTGTCCTTCCCACC | 221178 |
rs371158942 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24213046 | ACACCTGTGTGCTGC[C/T]CTGCTTGGGTCGGCC | 221178 |
rs371187650 | snp | C/G | 0.000133324 | 0.0081636 | missense | SPATA13 | GRCh38.p7 | 13:24286368 | GTGAAGATAAGGAAG[C/G]CTGGTTCCCCGCGAG | 221178 |
rs371192340 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987326 | AGGAGCCACACTGCT[C/T]GTAAAATACTTACAT | 221178 |
rs371196530 | snp | C/T | 3.58179e-05 | 0.00423175 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302555 | TTTCTGGTTAACAAG[C/T]GACCCTCAGTCCCTG | 221178 |
rs371204590 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074648 | GTGATTAAAAAAAAA[A/C]CCCTTGTAGGAATTA | 221178 |
rs371209190 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24281463 | GCTGCTCCAAGGTTC[C/T]CTGGCTGTCGCGGTG | 221178 |
rs371221770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253068 | TTAGTGACTGTCTTT[C/T]TGTCACTCACCCAGG | 221178 |
rs371244694 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272233 | TCCACCGCCTTCCAC[A/G]CAGGGGAGGCCGAGG | 221178 |
rs371250814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254010 | TCCGGTTTATGCTTA[G/T]AGAGGGAGGGCAGTT | 221178 |
rs371265729 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224415 | CACAGTGCCCTGTCC[A/G]CGAATTCAGAGGAAA | 221178 |
rs371275777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019545 | TATGTGTATTTTAAA[A/G]CATTTTTAATATCAC | 221178 |
rs371279268 | in-del | -/TTG | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297037 | TTGTTGTTTGTTTGT[-/TTG]TTGTTGTTGTTGTTT | 221178 |
rs371284065 | in-del | AT/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998928 | TTTTCACTAACTTTG[AT/G]TTTTTTTTTTTTTTT | 221178 |
rs371294956 | snp | A/T | 0.000165025 | 0.00908213 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294871 | CGTGGGCTGGGAGGT[A/T]AGTGGAAAGCACCCC | 221178 |
rs371299652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168135 | TTAATTAAATCAAAC[C/T]CCATGCAGCAATTAT | 221178 |
rs371321815 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229286 | TTAAATGATGACAAC[A/C]AATTGGACCCCTCTC | 221178 |
rs371334900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066843 | CTCTGTGGCAGCCAG[A/G]TTCAGAGACTCCGGC | 221178 |
rs371339184 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082855 | AAAAAAAAAAAAAAA[-/T]AAGATCTTTGCATTA | 221178 |
rs371351630 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023399 | CTGATTTGGATACTT[G/T]GCTTTTTATCTTCTA | 221178 |
rs371360420 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24266951 | TGTGAGCCACCAATG[C/T]CCAGCCAGGATTTTA | 221178 |
rs371373553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994333 | GAATGGAGCTTCAGT[C/T]CTCAGATGGAGCTTC | 221178 |
rs371374825 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292009 | GATCCACCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 221178 |
rs371388242 | in-del | CCCC/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116777 | CCTACCAGCCCCCCC[CCCC/G]CAATGTGCTGATGTT | 221178 |
rs371396459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002428 | AGTCGCTCTGCATTC[C/T]ATAGAGAGGGGACAG | 221178 |
rs371433790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134463 | CTACATAGAGGTCGT[A/G]TGGATGCCGAGAGCA | 221178 |
rs371442953 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295647 | CAAATACAATGCCTG[C/T]AATAATGGTCCAACA | 221178 |
rs371445233 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24012845 | TCTGTTTGGTTTATG[C/T]GTCTGCAGGTCGGGG | 221178 |
rs371445804 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306497 | CCAAGTCAACTAGGT[C/G]AAACTACTAGCAGAC | 221178 |
rs371456399 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277300 | ATACAAAAAATTAGC[C/T]GGGTGTGGTGGCGGG | 221178 |
rs371468142 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134130 | AACTCTGCCAGGTGA[A/G]AAATGCCAAGAGAGC | 221178 |
rs371473035 | in-del | -/TGA | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116788 | CCCCCCCCAATGTGC[-/TGA]TGATGTTTGGAGAAA | 221178 |
rs371493095 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24114120 | TGTAGAAGGACAAGT[A/G]TAGACTTTGGTTAGA | 221178 |
rs371493211 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082647 | AACAAGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 221178 |
rs371501038 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24076973 | TTCCAGGGGGATACG[G/T]CAAAGTCCTTCCCTT | 221178 |
rs371511214 | snp | A/G/T | 0.000299937 | 0.0122426 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249619 | GCCAGCTGGCCAGCC[A/G/T]CAGTTTGTCTATTCC | 221178 |
rs371514088 | in-del | -/TTCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997557 | CCATTTTGCATTGCT[-/TTCC]ATAGAGAAATACCTG | 221178 |
rs371535457 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174683 | CCAGGTTCAAGCTAT[C/T]CTCCTGCCTCAGTCT | 221178 |
rs371535795 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103258 | TTACCAGTTTATTTT[A/C]TTTACCTATGTCTAG | 221178 |
rs371547922 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046311 | GCCTTTTTTTTTTTA[A/T]GAGTCAGAGTGTCGC | 221178 |
rs371556296 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197932 | TGCATTTGCTTCTCA[A/G]AAACAGAACTGTTGT | 221178 |
rs371568296 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142062 | ATTGTGGTTTACGGT[C/T]CTGATATTAGAGCAA | 221178 |
rs371569783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169208 | TCGGTGGTTGCCTGA[A/G]TTCCAGCTCTTGGCT | 221178 |
rs371571219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121263 | TACCACTAAACCCTT[C/T]TTACATACCGAATTC | 221178 |
rs371575123 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208429 | GAAACAGTGTAATTC[A/G]TAATCCCCAGTGCTC | 221178 |
rs371576791 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000529 | GCCTTCTAGGGGGAA[C/G]ACAGGCCACAAACCA | 221178 |
rs371600312 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065354 | AGCAGATGGGAGGCA[A/G]AGCATGTGTGGGAGG | 221178 |
rs371601955 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010795 | AGGCAGGGCCAGTGC[C/T]TTGTTGGTGGATCTG | 221178 |
rs371623177 | snp | A/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270294 | TATGCCTTTACATGT[A/T]TACCTTTTGAACAAA | 221178 |
rs371637602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126261 | ATTGAGTCTGGGGGA[A/G]GGGTAGCTGGAGGTG | 221178 |
rs371641360 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207220 | TGGGGTCTGTCTGAG[G/T]GTTGGGGATGCAAGG | 221178 |
rs371655821 | in-del | -/ATATA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189726 | AAAAGCATATATAAT[-/ATATA]ATATATTATATATAA | 221178 |
rs371669327 | snp | A/G | 1.6836e-05 | 0.00290133 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284113 | TGTCTTTTAAATCAT[A/G]CCTTTGTTTTGTATG | 221178 |
rs371674658 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022657 | AAGAATTTTTTGGGG[-/G]CTAAAACAAGAAGAA | 221178 |
rs371717559 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198070 | GCATGATCTCTGCTT[A/G]CTGCAACCTCCACCT | 221178 |
rs371749849 | snp | A/G | 6.59109e-05 | 0.0057403 | missense | SPATA13 | GRCh38.p7 | 13:24297448 | GCAAAAGCCAGCAGC[A/G]GACGTTCTTCCTGTT | 221178 |
rs371753463 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24234402 | GACTAAGAAACTGAT[C/T]TCAGTATACGTTTTT | 221178 |
rs371755316 | snp | A/G | 0.000875616 | 0.0209055 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219039 | TTCATTCTAAAGTTC[A/G]TACACCCTAGAATCC | 221178 |
rs371764029 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010348 | CTTTGTTCCGCATCT[A/G]TGAAGATAAGCCATC | 221178 |
rs371767882 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306155 | TTATTCAGAAAATCC[C/T]CCCATCCTACATGAC | 221178 |
rs371786317 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24179631 | ACTCCCAGCCCCTGG[A/C]AACCTCTATTTTACT | 221178 |
rs371788710 | snp | A/C/T | 4.95383e-05 | 0.00497666 | missense, synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286887 | GCAGATGCGGACCAA[A/C/T]GTCATCCGGGAGATC | 221178 |
rs371791869 | snp | A/G | 0.000213459 | 0.0103288 | intron-variant, missense | SPATA13 | GRCh38.p7 | 13:24278726 | TCATCCACATTCAAC[A/G]GGTGAAAAAACAAAG | 221178 |
rs371792820 | snp | C/T | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158805 | TCACCGGCTCACTGA[C/T]GAGGAAGCTGAGATT | 221178 |
rs371794702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168642 | CACTCGCGTTACCCA[C/T]GGACTGAATAGGGTT | 221178 |
rs371801300 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24222768 | CTTCTGTGAGCAGAG[C/G]GGCTACTGCGTGGGA | 221178 |
rs371809458 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101496 | TTGTGGTGAAAAAAA[-/A]CAACACATAAAACTT | 221178 |
rs371816152 | snp | C/T | 0.334412 | 0.235318 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190066 | ACATATAATGATATA[C/T]TATATATATTATTAT | 221178 |
rs371838136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122664 | ACTTCAAGATACTTG[G/T]TGACAGACAGAAGTG | 221178 |
rs371844524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286603 | GTGGTCCTCGTGCCT[A/G]CTGGCATAGCCGCAG | 221178 |
rs371847585 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030065 | ACACACACACACACA[C/G]GCACACACACACACA | 221178 |
rs371862175 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189257 | CCGGTGGATCACGAC[C/G]TCAGGAGATGGAGAC | 221178 |
rs371879099 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24256643 | GAACTTGGCAGCGCC[A/G]TGCTGTGCTCTTCCT | 221178 |
rs371891190 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229418 | TGAACTTCTCCTGCC[A/G]TGGGTCTTCTCAAGG | 221178 |
rs371907037 | in-del | -/GG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208781 | AAGTGTGGAGAGAAA[-/GG]CAAGGAGAAAGTTCA | 221178 |
rs371911363 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24096042 | AGCTAAGCCTGGTGG[C/T]GTCCTTTATCTCCCA | 221178 |
rs371935820 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220281 | CCTTGTTTCCTTCTT[C/G]GTTATAAAAGGTCTT | 221178 |
rs371938829 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254737 | ATCATCAGCTTTGTT[A/G]AGGGGAAGGCCCAGA | 221178 |
rs371963239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266088 | AAATCCTCCTAGAGA[A/G]GTCAAGTGCTGACTA | 221178 |
rs371964223 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143011 | CACACAGAAGCTGAC[C/T]CTGAGACAATGGCTT | 221178 |
rs371972167 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24061908 | AAAAAAAGAAAAAAA[-/AA]CTGAGGCTCAGAGAA | 221178 |
rs371972375 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24287365 | ATAGGGTCTCACTGC[A/G]TTGCCGAGGCTGGTC | 221178 |
rs371976712 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155279 | TGGTGCTCCATCCCC[A/C]GTGACAGAGATCTGT | 221178 |
rs371981698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275955 | CTCCCCCAAAAAATG[C/T]TTTTTCCACACCAAT | 221178 |
rs371984378 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219121 | TTCTGTTCTCTTCCT[A/G]TCTCTGGCAGAGTTC | 221178 |
rs371988540 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189664 | ATTATATATTATATA[-/TTT]ATATATTATATATAT | 221178 |
rs371998266 | in-del | -/TTTG | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026569 | ACTGCTGTTTATTTA[-/TTTG]TTTATTTTTTATTTT | 221178 |
rs372015887 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24246694 | GAAACCGTGTCTCTG[C/T]TAAAAAATGTATATC | 221178 |
rs372017362 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098615 | AAAAAAAAAGAAGAA[A/G]AAGAAAAGAAAGAAA | 221178 |
rs372019058 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063716 | CAGCCTTCTCGTTGC[C/T]GATGTTTCACCCTTT | 221178 |
rs372020418 | in-del | AA/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993146 | TGAACCTGCTGTGGC[AA/G]AAGGTCGTGGACAGA | 221178 |
rs372029961 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134531 | TAGCAAAGCATCCCA[A/G]TGGGAAATGCTTCCA | 221178 |
rs372041520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137239 | CCCTTTGGGCTTCAG[C/T]TGGGGTGAAAGGCCA | 221178 |
rs372047788 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172370 | ATTTTGATGAGGTCC[A/G]GTTTATCAGTTTTTC | 221178 |
rs372059575 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084020 | CATTTCTGTTGCCTA[G/T]TCTGAAAGTGGAAGG | 221178 |
rs372059744 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24061726 | CTAATTGAGAGTGGA[C/G]TGTGGGAGGAGGGAG | 221178 |
rs372079653 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24130081 | CTTTCTGCCCAGAGT[A/G]GTGGTGAACACACAG | 221178 |
rs372084912 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300284 | TCTTTGAGGATTAAG[A/G]TTCTCTGTCTCAGGT | 221178 |
rs372089704 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24094997 | TATGTAAAACATGGA[A/G]ATTTCTCAGAAAGTT | 221178 |
rs372097032 | in-del | -/TCTG/TCTGA | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254198 | TGATTCACTGTGGCC[-/TCTG/TCTGA]AGGACTGTGAACTCT | 221178 |
rs372109981 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207300 | GGTGATAGGATGATA[C/T]GTGCAGCAAACCACC | 221178 |
rs372130157 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303605 | CCCACATGCTGTAAC[C/T]TAAGAAACTGCTATG | 221178 |
rs372134043 | snp | C/T | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24222944 | CATGACCCAGGCTGC[C/T]GTGCGGCCCTGGGCA | 221178 |
rs372136276 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166278 | AGGGAGAGGCCCATA[A/C/T]GTAAAAGCAAAGCAG | 221178 |
rs372151948 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023968 | GCTAATATCATAGTC[A/T]GTTCACAGCAAAATC | 221178 |
rs372152018 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029082 | TTATTTTTAATTATC[A/G]AATTTATTTTTAATA | 221178 |
rs372157304 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24259935 | GTGAGCCACCACACC[C/T]GGCCTGAGTTGGATT | 221178 |
rs372164997 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24130589 | CAGACAAGATCAGAA[G/T]TTTAAAGGTGGCCAG | 221178 |
rs372198199 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24069653 | GACTTAACTTTGTTT[G/T]TATTTTTCTTAATTT | 221178 |
rs372213309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035644 | ACAGGAGGCGTGTCA[C/T]TGAGTTGTACTTAGT | 221178 |
rs372213690 | in-del | -/GTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148920 | TTTCCATGAGTGTTT[-/GTTT]ATACCAGGAAATGCT | 221178 |
rs372216145 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101423 | TCATCCAGCTTGGAT[A/G]CTTTTTTCTTGTAAC | 221178 |
rs372224850 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24106983 | GATAGGATTCTAGTG[C/T]ATTTGCTCTCTGAAA | 221178 |
rs372237944 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084175 | AACTTAGCAACAAGC[A/G]AGACGAGAGAAGAAA | 221178 |
rs372260294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015718 | TTCCTGATCCTTCCC[C/T]TTTGGGGCGACCCCT | 221178 |
rs372263116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086582 | TGGCGAGAAGGTGGA[A/G]TAGAGGAGGCAGAGG | 221178 |
rs372271668 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189920 | TATTACATAATATAT[A/T]TTATATAATTATATA | 221178 |
rs372279434 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24129785 | GCTTACCATGTGGCC[A/G]AAGCCTGCCTCAGTC | 221178 |
rs372283758 | snp | A/G/T | 0.000225299 | 0.0106114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286981 | GGGACCTCACTGAGG[A/G/T]TCACAGTATGAGGCT | 221178 |
rs372284324 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046324 | TAAGAGTCAGAGTGT[C/T]GCTCTGTCACCAGGC | 221178 |
rs372304811 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295339 | GTACAGGCCAGGCAC[A/C]GTGGCTCACACCTGT | 221178 |
rs372309211 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285340 | AGATGTGAGGGACTT[-/C]CAATAGCATATGTGC | 221178 |
rs372314379 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23982395 | CCTGAAGGCAAGGAC[A/C]AGGTCTTCTGTGTCT | 221178 |
rs372318323 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995122 | AAAAATGTCAGTAGT[G/T]CCAAGGTTCGGGAAC | 221178 |
rs372318619 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142111 | ATTTGTAGGGAAAGG[G/T]TTTTTTTTTTTAGCT | 221178 |
rs372339529 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24120996 | AACGATAACGAGGAA[G/T]TAGGAGTGCTTGCTT | 221178 |
rs372365186 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989297 | AGTAGTAGCATGCGC[C/T]TGTAGTCCCAGCTAC | 221178 |
rs372365193 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113891 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAATAT | 221178 |
rs372371474 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24014654 | TTGTAACAAAATAGT[G/T]TATGTCTTCTCCTAA | 221178 |
rs372376733 | snp | C/T | 0.00018797 | 0.00969276 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223348 | CAAAGGGAGAGGCTT[C/T]GGAGCATGGCCTGGG | 221178 |
rs372385362 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211669 | GGTCAGCAGGCCATG[C/T]TGACTCTCTCCCCAT | 221178 |
rs372411019 | in-del | -/CATT | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031071 | CTCAATATCTTCTCC[-/CATT]CAAAGTAGCAAATGG | 221178 |
rs372411452 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983657 | GTTGTTTTTTTTTTT[-/T]AAAAAACATCCAGAA | 221178 |
rs372421924 | snp | A/G | | | missense | SPATA13 | GRCh38.p7 | 13:24302676 | TCACTATGCCCACAA[A/G]CGTCCCCCAGCAGCA | 221178 |
rs372435214 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154730 | CTCAGGGCCTCATGA[G/T]GCTGCTGCCACAGTT | 221178 |
rs372454768 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228259 | GCTGGGACTACAGGC[A/T]CCTGCCACCATGCCC | 221178 |
rs372476986 | in-del | -/CTCT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057029 | TCTCTCTCTCTCTCT[-/CTCT]TTCTTTCATAGCGTC | 221178 |
rs372477660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167600 | TAGTGTGAATGGGAA[C/T]GTTATGTGAATTGGG | 221178 |
rs372494771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139655 | CTGGAACTACAGAAA[A/C]CCTCTCTGAGCTTGG | 221178 |
rs372509854 | snp | G/T | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286788 | GAATCAGGAAGAGCT[G/T]TCGGAAAACTCCAGC | 221178 |
rs372542668 | snp | G/T | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160092 | GGCCCTGGGAAACAT[G/T]TAGGTTTAAAAATCC | 221178 |
rs372551990 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140423 | GAACTAGTAATTCAT[C/G]TATAGAGTTTTCATT | 221178 |
rs372553137 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240075 | TTTGGGAGTCTGAAG[C/T]AGGTGGATCCCTTGA | 221178 |
rs372555610 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24224939 | GACTCATATCTTTCT[C/T]CTTTGTATTTTAAGC | 221178 |
rs372557670 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029204 | CTGGAACTTACAGGC[A/G]TGTGCCAACACAGCC | 221178 |
rs372577070 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292965 | CGCACCATTGCACTC[-/C]AGCCTGGGTGACAGA | 221178 |
rs372595343 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277220 | GAGGCCGAGGCGGGC[A/G/T]GATCACAAGGTCAGG | 221178 |
rs372598924 | in-del | -/CTTAGATA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095630 | AAAAAGAAAAACCAC[-/CTTAGATA]CTTAGATAACAGTAA | 221178 |
rs372601879 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258702 | CTGAAAAGTTAGAGA[C/T]ATGAGTGAGGAATAA | 221178 |
rs372605283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260577 | TATGAGACTGAAAGG[A/G]GACTTGGCATCTCTG | 221178 |
rs372630721 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272628 | GGCGGGTTTATGGGT[C/T]GTCTGCCATCTTATG | 221178 |
rs372642439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991394 | AAAAATAGCAAAGGT[C/T]ATATTTTACTGCACT | 221178 |
rs372656030 | in-del | -/GAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232258 | AGTGTTCCTGGGCAG[-/GAG]AAGGTGGATGTCTGC | 221178 |
rs372659229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145992 | ATCTGTCTGCAGCTG[A/G]ATGTGGTGAGGAGTG | 221178 |
rs372663258 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239463 | ACTTTGGGATGCTGA[C/G]GCGGGTGGATCCCTT | 221178 |
rs372676441 | snp | C/T | 4.94401e-05 | 0.00497168 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24290789 | GCAGATGATTGACAT[C/T]GCCATCGACGGGTTC | 221178 |
rs372683188 | in-del | -/TATATGAATATTAGCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065549 | CAAGACAGCGTGGCA[-/TATATGAATATTAGCA]AGTAACATGGAATTG | 221178 |
rs372686533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276154 | GCAGGGTCTCAAAAA[G/T]ATAGTAGCACATTAC | 221178 |
rs372702980 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133086 | CAACATTAGCAATGG[A/T]TTCCCACGTATTTCC | 221178 |
rs372705251 | snp | G/T | | | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307533 | TGTTTGCTGTGGCTG[G/T]AATCAGAAAAGGATT | 221178 |
rs372714356 | snp | C/G | 1.6519e-05 | 0.00287388 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24251810 | ATTCTCCCAGAGCAC[C/G]CCCATTGGGTTGGAC | 221178 |
rs372720852 | in-del | -/GAG | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253765 | AGAGATCCGAGGGAG[-/GAG]AAGTCCTAGCCGAAG | 221178 |
rs372736561 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150311 | GCATCACTGCTGCAC[A/G]GCTCCTGCCAGTCCC | 221178 |
rs372739095 | in-del | CCC/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116778 | CTACCAGCCCCCCCC[CCC/G]CAATGTGCTGATGTT | 221178 |
rs372742681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130355 | CCTGTAACTGGATCA[A/G]AAGGGGACTGTTTGG | 221178 |
rs372749428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113340 | AGGTGCAGTGGCTCA[C/T]GCTTGTAATCCCAGC | 221178 |
rs372763429 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169925 | CCTGCCTTCTGATAC[A/G]GAGATTGTCTTGGAG | 221178 |
rs372766436 | snp | A/G | 5.03952e-05 | 0.00501947 | missense | SPATA13 | GRCh38.p7 | 13:24286232 | ATCAGTGATGGCAAC[A/G]TGGTCTGCGCAGAAG | 221178 |
rs372768109 | snp | C/T | 0.000195446 | 0.00988356 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224494 | CCTTGCAGGATCCCC[C/T]GGAAGCCACACATGG | 221178 |
rs372775736 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188345 | TCCAAAAAAAATAAT[A/T]AAAAAAAAAAGTGAT | 221178 |
rs372778399 | snp | C/G | 0.00106216 | 0.0230206 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286437 | AAAGTACCTGGGGGA[C/G]CTGCAGGATCCTTTC | 221178 |
rs372780086 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189736 | ATAATATATAATATA[A/T]TATATATAAAAGCAT | 221178 |
rs372780315 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074765 | GGAAGATTCTTGAAT[C/T]GGGCAGCACAACCTC | 221178 |
rs372788479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131611 | AGAACAACAGAACCA[C/T]GTACTTGAAGTGGAA | 221178 |
rs372792074 | in-del | -/AT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189887 | TAATTATATATCATA[-/AT]ATATATTATATAATT | 221178 |
rs372818854 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24012589 | TCTTCCCCTCTCAGG[A/G]GCTCCCCTGGTTGAT | 221178 |
rs372819675 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021771 | GGCTGGAGTGCAGCG[A/G]CATGATCTTGGCTCA | 221178 |
rs372857664 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063218 | TATTCGCGTCTGCCT[A/C/T]CTCCTTGCCAAACCA | 221178 |
rs372862015 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24007183 | GGCCTGTGCCGGTTG[C/T]CTGGTGGCCCTGAGG | 221178 |
rs372869728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057810 | AGCCCAGCCTTCCCC[G/T]TGGAGGTCCAGGGAG | 221178 |
rs372873532 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192092 | TCAGGCTTCTACCCC[C/G]ATCTGTGGCTCCACC | 221178 |
rs372887074 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227190 | ACTCGTAGTTTGTAA[A/C]CTCCCCTCCCTAAAA | 221178 |
rs372889481 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293184 | AAAGAAGAGAGAGCT[A/G]TATATTTTTTTCTTT | 221178 |
rs372889856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032425 | CAGTCCACATGGTAT[G/T]ATTCTTAACAACCAC | 221178 |
rs372897394 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036717 | GTGAAGGCTGCTCTC[A/G]CCTTACTAAACAACA | 221178 |
rs372917240 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992481 | TGCTGGTGGTGGTGG[-/G]ATGGCTCTGCTCCAC | 221178 |
rs372923880 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242765 | CTTATCTCTTTCTGC[A/G]TATGTAAATATTTCC | 221178 |
rs372924023 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24167890 | GTTGAGCAACTGCAT[C/T]GGCCCTGACACTGAG | 221178 |
rs372957214 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160646 | ACCGGGGGCGTGGCC[A/T]GATATGGGGCGGGGG | 221178 |
rs372965443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044962 | GTTAGATAGGAGAAA[G/T]AAGTTGTGAGCCTTT | 221178 |
rs372983856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222496 | CCATTTCAAATAAGA[A/G]GAAAAGATAGTGTTG | 221178 |
rs373001683 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24091410 | ACTTCAAAACGCTGC[C/T]GTGTTAAACAATTGC | 221178 |
rs373007959 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175231 | GATGCTTGTTTTTTT[G/T]TTTTTTTTAATTTGT | 221178 |
rs373012939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221107 | AGTCAGATGCCTGGG[G/T]TACAGATGCCCATTG | 221178 |
rs373019073 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057029 | CTCTCTCTCTCTCTC[-/TT]TCTTTCTTTCATAGC | 221178 |
rs373035664 | snp | C/T | 8.98674e-05 | 0.00670266 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223661 | GAGGGACCCTGAAAA[C/T]AACAGCATGGGCTAC | 221178 |
rs373055949 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080214 | TCTCCTTCACATGAC[C/G/T]GTATGTCAAAACAGC | 221178 |
rs373061910 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180530 | AAATCATGCAAAGTC[A/G]TCAGCCAGGATTTTG | 221178 |
rs373090481 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164346 | CTCTGCTCCCTCCAT[A/G]TTTAATGCCTCTTTT | 221178 |
rs373104805 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24231645 | TGCTAGGTCTTGTGA[C/T]ATTTCTATGTTTAAT | 221178 |
rs373116245 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068297 | TTGCTAAGGATAATG[A/G]CCTCCCTACAGAAGA | 221178 |
rs373124585 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24268575 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCTCATC | 221178 |
rs373128424 | in-del | -/GGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23988858 | TTCTTTATATTGGCT[-/GGG]GTTGTTGAAAAATGT | 221178 |
rs373151219 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081597 | AAGGATTGCTTGAGC[A/G]CAGGAGTTCAAGGCT | 221178 |
rs373157511 | snp | C/T | 0.00027828 | 0.0117925 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223628 | TGGCCAGGTGCCCGC[C/T]GTGTGTGAGATTCTC | 221178 |
rs373161710 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211817 | AGGCCTAGGCTCCCC[C/G]ACCCTGTCCCTGCCT | 221178 |
rs373168186 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104467 | ATTTATTCAAATATG[A/C]AGTTAAGGGAAAGTA | 221178 |
rs373172526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248634 | TCCTCGTTCAGTGCT[C/T]GCCCCATCAGACTGC | 221178 |
rs373185574 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034654 | ACTTGGACCACAGTC[-/A]TTGGGAGGTTCACCA | 221178 |
rs373187163 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284497 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAA | 221178 |
rs373193177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273281 | GGGGTCTGGAGCCAA[A/T]GGGGTGTTGGCTGCC | 221178 |
rs373201313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255175 | ATTGCTTACATTTGC[C/T]GCCGGGAGTTTCCCT | 221178 |
rs373205459 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233254 | ATTATGTGTGCTTTC[-/A]AAAAAATGTTTTTCT | 221178 |
rs373207807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004649 | CAGGTGTGGTCAGCA[C/G]AGTGCATCAATTAAA | 221178 |
rs373209733 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036186 | CATTACATAAATTCC[A/T]TATTGTTATGAAAGT | 221178 |
rs373219409 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019629 | TTTCTTCCTCTTGTG[G/T]GTACTTTATAATTAG | 221178 |
rs373241251 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980286 | AAAGCCAGCCTGGCG[A/G]TCGCGTTGCCATGGC | 221178 |
rs373256869 | snp | G/T | 5.31599e-05 | 0.0051553 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284299 | CACACGACAGTAGTG[G/T]ATACGGGATACCTGA | 221178 |
rs373262165 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248446 | TGTGCTTTTCTGGTA[C/T]ATTGTGTTGCCTCTG | 221178 |
rs373269830 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295954 | ACCCTGGCTTCAAAG[G/T]CCGTGCTGGTGATCA | 221178 |
rs373285061 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185818 | ACATACATCAAGAGA[C/G]AGAGAGAGAGAGAGA | 221178 |
rs373288962 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118921 | CTTTTCTTTTTTTTT[C/T]TTGAGATGGAGTCTT | 221178 |
rs373290103 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154533 | TTGCTAACGGGGGGG[-/G]AGGGGCACATAAGGG | 221178 |
rs373299531 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979849 | CTCCGTGACCTTCCT[A/C]CCCCTTCCAGCTCGG | 221178 |
rs373337603 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24229934 | TAAAAGCAAAATGCT[A/G]TGGGTTTCAGAGGAC | 221178 |
rs373337994 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307257 | AAGGGGGGCTCCGAG[G/T]GCAACCTCGGAGGGC | 221178 |
rs373339565 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015949 | ACGCTTCTGTCCTTC[C/G]TCCTTCTGCCCTCGG | 221178 |
rs373344313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248164 | CCTCTCTGGCCAGGC[C/T]TTGAGGGGTCTGCTC | 221178 |
rs373344938 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059142 | ATGTCCTGCTAATTT[C/T]TTGTATTTTTAGTAG | 221178 |
rs373345020 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978627 | CATCTATTTATATTT[A/G]CTTTTTTTTCAGGGA | 221178 |
rs373360129 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066605 | TGGAGGGGACAGCAG[G/T]TGCTCACTGTGCTCA | 221178 |
rs373363931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011055 | TGGGATATGCCTGCA[C/T]TCTGCAGTTTGCTGA | 221178 |
rs373370640 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119670 | CTTTGTCTCATCTGT[G/T]TCTTCTAACTTAGCA | 221178 |
rs373375343 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270208 | TTTGGAAAGTATAGA[A/G]GAGTATAGAGGAAAT | 221178 |
rs373376697 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278523 | GCTCAAGGGATCCTC[C/T]TGCCTCAGTCTTCCA | 221178 |
rs373377871 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108921 | TTAAAAATCTCTCTT[C/T]CCTGCTTGTAGCCCA | 221178 |
rs373380366 | snp | C/T | | | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252939 | CAGTGAGCACTTTAT[C/T]TGGGTATCCAGTGAG | 221178 |
rs373414745 | snp | C/T | 0.000107302 | 0.00732389 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224555 | CATTGGTGTGGCAGC[C/T]GGCCCAGAAGAAAAG | 221178 |
rs373419697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107057 | ATGATAAGGACGGGG[A/G]AAAAAAAAAGGAAGA | 221178 |
rs373448208 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24016820 | GGCCTGGCTGCTGCA[C/T]GATAACATGAGCCTG | 221178 |
rs373458625 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303747 | CCAGTCTCTACTAAT[A/C]ATACAAAAATTAGCT | 221178 |
rs373458769 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074831 | ATGCTGCCACGTGGT[C/T]AGAGAGGATTTCTAG | 221178 |
rs373482330 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24273093 | CCCCAGGACGAGCAG[A/C]TCCTGGCTAGGAACA | 221178 |
rs373482395 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138740 | AGGCTTGTGCCACCA[A/C]CCCTGGCTAATTTTT | 221178 |
rs373484011 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190123 | ATTATTATATAACAT[-/A]ATAATATACAATATA | 221178 |
rs373487728 | in-del | -/CTT | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084071 | CAAGCGTTTTTACTC[-/CTT]CTTCTCAGAAAGAGA | 221178 |
rs373508738 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983252 | TTTTTCTGACGCCGC[G/T]CTCCTTGGCTCACAA | 221178 |
rs373570549 | in-del | -/G | 0.0887219 | 0.191022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291947 | ATTTTTAGTAGAGAC[-/G]GGGTTTCACCTTGTT | 221178 |
rs373573628 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225393 | GCGTGTGGACGAGGG[A/G]AACGTGGTGACGAGT | 221178 |
rs373586803 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043053 | TTGAGTGGAACACAC[A/C]CAAACTCATTAAATT | 221178 |
rs373595594 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235975 | GCATTCAGTTTTCAC[A/T]GCCACTTGTGACATA | 221178 |
rs373609675 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189732 | ATATATAATATATAA[C/T]ATATTATATATAAAA | 221178 |
rs373612208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153989 | CACATCAACTCTGAG[C/T]GGTGGGAACTATTGT | 221178 |
rs373631398 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277255 | CGAGACCATCCTGGC[C/T]AACATGGTGAAACCA | 221178 |
rs373634223 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040685 | AGAATCCAACTAGGC[C/T]TCCTCTCCTGTGGAT | 221178 |
rs373655602 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211922 | TCCGTGTGTCGGCTG[A/C]AGGAGGCCACTTCAG | 221178 |
rs373661910 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207455 | CTCCAGAAGTGGAAT[C/T]GCTAGAGCATGTAAT | 221178 |
rs373663960 | in-del | -/T | 0.411004 | 0.191253 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199019 | GTGGTTCATTCTTTG[-/T]TTCTCTTTTCAGGCA | 221178 |
rs373674664 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118353 | AATTGCTTATGCATT[A/G]CTGAAAATTACAAAA | 221178 |
rs373677211 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138284 | CCAGTCCAGCCCAGG[C/G]GACAGAGCAAGACTC | 221178 |
rs373697734 | in-del | A/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227304 | TCATTGAAATATTTT[A/TT]TTCCTGAGAACCTGT | 221178 |
rs373713937 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24177736 | GGGTTACAGGCATGA[C/G]CCTGGCCATTGGGCC | 221178 |
rs373733402 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011320 | GAGGCAGTGCCGGCC[A/G]GCTTGGCCATCTCAT | 221178 |
rs373733596 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147155 | GAATGCTTTTTCCAC[G/T]TATAATTAAAATTGT | 221178 |
rs373735134 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121819 | GTCAGGATCTTCCTT[C/T]CTTCAAAAAATAAAG | 221178 |
rs373764359 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277304 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 221178 |
rs373812815 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24178440 | CCATTATCTTATGAC[A/G]TCACTTGTATACAGT | 221178 |
rs373813922 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980897 | GCGCCTGGCCAACAA[A/G]GTTTTTTAAAAAATA | 221178 |
rs373820619 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044225 | ATTTAATTTGTTTTT[C/T]TTTCTTTCTTTTTTT | 221178 |
rs373824193 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115511 | CGTTGCGTGCTCCTT[A/C]TGAGAATCTAACTAA | 221178 |
rs373825933 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273981 | AGGCATGAGCCACTG[C/T]GCCCGGCCAATGGTT | 221178 |
rs373830605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226093 | GGCTCAGAATGGAGG[A/C]AGTGCATGCTGATTG | 221178 |
rs373831317 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117203 | TACATTGTAGATGGA[A/C]TAACAAATCTACATA | 221178 |
rs373840828 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24299215 | AAAGACGGCACTATT[C/T]AGTGGGGGCATCCTA | 221178 |
rs373843397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998729 | TTTAGGTCTATGATT[C/T]ATTTTCAGTTAATTT | 221178 |
rs373852174 | snp | A/G | 9.94151e-05 | 0.00704966 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24251720 | TTTCTTTTTGCAGCC[A/G]GCTTCCAGGCCGCCC | 221178 |
rs373875230 | snp | C/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190154 | TATTATTATATAACA[C/G/T]ATATATAATATATAT | 221178 |
rs373876833 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24096324 | AGGAGGCCTGGGTGC[C/T]GTGGCTCACGCCTGT | 221178 |
rs373879959 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24210313 | TGCTTTTGTTGCCTA[C/T]GCTTTTAGTGTTATA | 221178 |
rs373896727 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116768 | TGTTGAAGCCCTACC[A/C]GCCCCCCCCCCCCAA | 221178 |
rs373900758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280589 | TGCTAAAATTGGAAG[A/T]TTCCTGCTGCTTTAG | 221178 |
rs373916574 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013763 | GTCTGCAGTGTTAGG[A/G]GTGCCACATGTGTTC | 221178 |
rs373920732 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24165164 | AGGACCTGACTTCTT[G/T]GTGAGCAATCACTTC | 221178 |
rs373928247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176909 | GCTGGGACCACAGAC[A/G]TGTGCCACCACGCGC | 221178 |
rs373944649 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24247130 | AACAGAGGTCACTCT[-/CT]AAAGCCTTCAGCTCA | 221178 |
rs373972796 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282307 | AAAGAACTCTTCAGT[C/G]AGAAACCAGACCCAT | 221178 |
rs374002408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274526 | TGTCAGTTCCTGTGA[C/T]CCAGCTCTTTCCCTC | 221178 |
rs374010267 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146399 | GATCACCGAGTACCC[C/T]TGTGATCGTTAGCTG | 221178 |
rs374012010 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143688 | CACAGGGAACCCGAA[A/T]CGTCCTCCAGGGGAA | 221178 |
rs374012604 | snp | C/T | 6.65923e-05 | 0.0057699 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24249740 | GAATGCTCCAGTGGG[C/T]TGCCCCAAAGGAGCC | 221178 |
rs374015338 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124551 | TAGATTCTGGTGAGA[A/G]TGGCAGTCCTGGAGG | 221178 |
rs374023423 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030372 | ACCCATAGGAGACTT[C/T]CCTTAAGAGCCAAGA | 221178 |
rs374058027 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189661 | TATATTATATATTAT[A/G]TATTTATATATTATA | 221178 |
rs374091437 | in-del | -/TCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24045123 | TATGTATAATTTATA[-/TCA]CTCATTGCCAATCCT | 221178 |
rs374097131 | in-del | -/TATGCCTTTACATG | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270278 | GTATACCTTTACATG[-/TATGCCTTTACATG]TATGCCTTTACATGT | 221178 |
rs374097665 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058044 | GCTTAATACACCCAA[A/C/T]GCAAGATGAGCTCCC | 221178 |
rs374123922 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230900 | TCAGGGCAGGGACTC[A/G]GAGGGACATTCCGTG | 221178 |
rs374137381 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198225 | GTCTTGAACTCCTGA[C/T]CTTGTGATCTGCCCC | 221178 |
rs374141507 | in-del | -/GG | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125997 | TGGCTTGGGCCCTGT[-/GG]TTCTTGGGGAGGTAC | 221178 |
rs374148418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111193 | CAGATACATGCATGA[C/G]CCACCACACACAGCC | 221178 |
rs374174087 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239941 | TTTAAGATGTGGTCA[C/T]TATGTGCATTTATTT | 221178 |
rs374176784 | snp | A/G | 0.000153988 | 0.00877328 | missense | SPATA13 | GRCh38.p7 | 13:24251829 | ATTGGGTTGGACCGT[A/G]TGGGACGCCGGCGGC | 221178 |
rs374200205 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992224 | CTGCTGCCTCCATCA[A/G]TGTCCAGGAGGTCTG | 221178 |
rs374207014 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24158069 | ACAACAACAAAAAAA[-/A]GCGCGTTAGACTTAG | 221178 |
rs374207596 | in-del | -/AGAGGGCTCG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272025 | CAGACCACATGAGTG[-/AGAGGGCTCG]GTAATGCTAGCGAGA | 221178 |
rs374240214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131315 | CTATGATGCTTCTTG[C/G]ACTTGTGCAGAAAGC | 221178 |
rs374241571 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237396 | AAAAACATGCTGCAG[C/T]ATGGCTGAACCTTGA | 221178 |
rs374245281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272750 | TTTGAATCCAGCCCC[A/G]CAACTTGGGGAAAGT | 221178 |
rs374246830 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24165548 | CCAGTCTCCTGCCCT[C/T]TTCTCCTCTCTCAGC | 221178 |
rs374260980 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224995 | TACATATAAGTGAAA[C/T]TCTTTCTGTTAAGAG | 221178 |
rs374270470 | snp | A/G | 0.000115589 | 0.00760138 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302786 | TGAAAACAGGAGGCT[A/G]TGCTTCCATGGAGCT | 221178 |
rs374278325 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24056907 | GGGGAAATGGAACTT[-/C]TTTTTTTTTTTTTTT | 221178 |
rs374278701 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023975 | TCATAGTCAGTTCAC[-/A]GCAAAATCCTGGTCA | 221178 |
rs374283418 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206910 | AAAAAAAAAAAAGAT[A/G]CATGCATGCATATGT | 221178 |
rs374287614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147575 | CTCAAGCTGTTAAGC[C/T]CCTTCCAGGAAGCCA | 221178 |
rs374288894 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151174 | GATGGCCCTCAGACC[C/T]AGATGCTTCCTCCCG | 221178 |
rs374297273 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134311 | ACCACACCATGAAAA[G/T]TGTAAGCCCTGGCCC | 221178 |
rs374299120 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24137538 | GCTGAGGCGGGAGGA[C/T]CACTTGAGGCCAGGA | 221178 |
rs374302610 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229489 | AGAGCCAGTGAAATT[A/G]TGGATGTCAAACACT | 221178 |
rs374302752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146628 | GGGCACTAAGGAAAT[A/G]GAAATGCACAGCAAT | 221178 |
rs374310474 | in-del | -/GGGGAAGAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24203339 | GGGGAAGGGGAAGAA[-/GGGGAAGAA]ATACTGATAATATAG | 221178 |
rs374323897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088862 | GTCCCCAAGGCTGGC[C/T]CCAGGAAAGCGCAAG | 221178 |
rs374326583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237095 | TGGGCGCAGGGCTCA[C/T]GTCTGTAATCCCAGC | 221178 |
rs374350296 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189850 | ATATTTAATATATTA[A/T]ATTAATATATCATAT | 221178 |
rs374351350 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143765 | CTGGCTACTTGATGC[C/T]ATGTCTTGCTATAGA | 221178 |
rs374353434 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24071795 | CTGTTTTTCTGGATG[C/T]CTGGAAGCTCTGTTT | 221178 |
rs374357321 | in-del | -/CAAACCTGCATCCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052059 | CCTGTGTTTGGACGC[-/CAAACCTGCATCCT]AGGGTTTGGCTTCTT | 221178 |
rs374371691 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24274297 | GTTCCCAAATTTTTC[C/T]AGGTGTCAGAATCAT | 221178 |
rs374398592 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112537 | CATTTTTGCATCCCA[C/T]TTCTTGTGCCAGGCA | 221178 |
rs374411183 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090645 | AGCTTCTTGACTGGA[C/T]TGCCCCAACTTACTG | 221178 |
rs374413770 | in-del | -/ATG | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189870 | TATATCATATATAAT[-/ATG]ATAATTATATATCAT | 221178 |
rs374418796 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24250457 | AATTAAAGACCCTAT[C/G]TTGGAGAAGTGTATA | 221178 |
rs374425118 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046952 | GAACAGGAGTTTATT[A/T]CTTTATTACTCAAAT | 221178 |
rs374428341 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026670 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 221178 |
rs374430717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084603 | GTGCTGACTGCTCAG[C/T]TCTGTCCTGAGGGTC | 221178 |
rs374452020 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126838 | GGGATTTGGTTACAG[A/G]CATGAGCCACTGCAC | 221178 |
rs374459486 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181457 | CTTTATAGCCTTATT[C/T]TTCTCTACTGTCCCT | 221178 |
rs374475799 | in-del | -/ATAATATAC | 0.358728 | 0.225118 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190252 | TATAACATATCATAT[-/ATAATATAC]ATAATATATATTATT | 221178 |
rs374487361 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074385 | CCACATTTTTTTTTT[-/T]ACCATTCATCCATTG | 221178 |
rs374489803 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019093 | TTATTATTATTATTA[-/TTT]TTTTTTTTTTTTTGA | 221178 |
rs374493986 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307037 | CTGTGAATCTATATT[C/T]GTTGTTTTGTATATT | 221178 |
rs374498267 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070938 | CCAACTCGTGCTGCA[C/G]ATCTTAGGACGTGCT | 221178 |
rs374508670 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24290500 | TGGCAGGGCAGCTTG[C/G]GTGCCAGCGGATTTC | 221178 |
rs374525308 | in-del | -/GTTGA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184563 | GTGTCTGTTTAACTT[-/GTTGA]TTTTTTTTCTCTCTG | 221178 |
rs374526267 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018991 | CATATCTGATTGAGT[A/G]GATCTCAACAGACAT | 221178 |
rs374527529 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103503 | AAAAAAAAAAAAAAA[-/C]AAGAAAGAAAAGAGC | 221178 |
rs374527546 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025196 | TTCCTATTTTTGTTT[A/C]TTTCCTAAAATTTTT | 221178 |
rs374530005 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24261143 | TGATCAGATGTGCAT[C/T]CAGAGAGATCATTGG | 221178 |
rs374531100 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022648 | AAACTAAAATAAGAA[-/T]TTTTTGGGGCTAAAA | 221178 |
rs374534423 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24286689 | CAGGAAAGTAGGAAC[A/C]TGGGAGGTCTCCTGC | 221178 |
rs374534469 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030811 | GAATCTCCAGTCTAC[A/C]ATATTGCCAGCAGTG | 221178 |
rs374548445 | in-del | -/AATTTTTGTAGCAGGC | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172523 | TGATCCATTCAAGTT[-/AATTTTTGTAGCAGGC]ATGAGATTTAGGTCA | 221178 |
rs374548763 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245525 | TTAGAGGGAATGTTT[G/T]CTCCTTTTATATCTT | 221178 |
rs374551345 | in-del | -/TTTGGGTATA | 0.0240643 | 0.107019 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109457 | CATGATTTATAATTC[-/TTTGGGTATA]TTTGGGTATATACCC | 221178 |
rs374568027 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24120951 | AGCTTCCTGGGGTCT[A/G]GGTCTGAGGAATAAA | 221178 |
rs374596629 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089314 | TGCATGGGACCCCCC[A/C]ACACACCACTCGGAC | 221178 |
rs374598854 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029389 | CAAATAGTGTGAAAT[C/T]AAGACCCAAATCCAT | 221178 |
rs374604265 | in-del | -/A | 0.473867 | 0.111281 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189647 | TATATATTTATATAT[-/A]TATTATATATTATAT | 221178 |
rs374616433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005544 | AATCCTTGGTGAAAA[A/G]GGGCCATTATACAGC | 221178 |
rs374617967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001250 | GTAACAGTGTTACAT[C/T]GCTGAGGTGGAGGGT | 221178 |
rs374626457 | in-del | -/AC/C | 0.474 | 0.111014 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098606 | CTTAAAAAAAAAAAA[-/AC/C]AAGAAGAAGAAGAAA | 221178 |
rs374632396 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24213642 | TACCATTCAAGCTTC[C/T]AAGTCAAAGATCCAG | 221178 |
rs374638014 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24214988 | TGTGTCAAAGGAGCC[A/G]TGTCCCTGGGATATT | 221178 |
rs374662226 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298435 | TTGTCTTCCCAGCTT[C/T]TGCTGACCTGGAGGT | 221178 |
rs374662974 | in-del | -/TT/TTT/TTTT | 0.251578 | 0.249995 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181761 | TGTTTTACAGTTGAC[-/TT/TTT/TTTT]TTTTTTTTTTTTTGT | 221178 |
rs374667373 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100012 | GGCTTCTGGTGTGGC[C/T]GGCACAGTTCTCTTT | 221178 |
rs374678681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116483 | TGGAGGGTGGCTGCC[A/G]CAGTAGCATTTCCTG | 221178 |
rs374680225 | snp | C/T | 0.000437904 | 0.0147905 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223254 | ACCCTCGCCTCCTTC[C/T]GGAAAATGGGATCCT | 221178 |
rs374722087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218603 | ACTTTGTTATCATGT[A/G]AATCAAGCTTCTCTA | 221178 |
rs374730758 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028882 | GTCATTTCTAAAAAT[A/G]TCCTTGCTCATGGCT | 221178 |
rs374758733 | in-del | -/CCCCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24145242 | TCTGATTTTTTACAA[-/CCCCC]CAGCCACAAAATACT | 221178 |
rs374765155 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151866 | ATAGTCTTTAACAGT[A/G]CTAAGCAGTATAGAT | 221178 |
rs374765674 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019601 | TTGAGCAGAATATTA[C/T]TAGTGCATTCTCTTT | 221178 |
rs374774381 | snp | A/G | 0.000141899 | 0.00842197 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302575 | CTCAGTCCCTGTTCC[A/G]TCTCTCTCCCCTCCC | 221178 |
rs374777613 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058322 | TCACTCACCTGATTC[A/G]GTCACTGTTTAAACC | 221178 |
rs374779440 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027272 | CCCAGGTAGCTGGGA[A/T]TACAGGCGTGCGCCA | 221178 |
rs374790490 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084134 | ATTGTAATGAGCTCC[A/C]AAGCCTGATCCTAAT | 221178 |
rs374797474 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306734 | GCACTGACATTTTAT[A/G]TTTAGAAAATACTTT | 221178 |
rs374801998 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229291 | TGATGACAACCAATT[G/T]GACCCCTCTCCAGGG | 221178 |
rs374803750 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283407 | TAGAGAAACAGTGAT[A/G]GAGACATCCCTGAAC | 221178 |
rs374808442 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983682 | CCAGAACTGAATTCT[A/G]TATCTAGCTTGCTTC | 221178 |
rs374821128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261595 | ATTTGGGGACCAGTG[A/G]AGGCAGAGAAATTCA | 221178 |
rs374825431 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282785 | TGCTAAAAGTTTCAC[C/T]TGCATTCTGTGGCCT | 221178 |
rs374828308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272513 | GGTTTTCTTTCCTTT[C/G]AGAGCTCTGAGAGGG | 221178 |
rs374840124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197117 | TTCCAGTTTTTATTA[C/T]GTTTCAGTCTTGAGA | 221178 |
rs374843944 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24261701 | GTGAGAGTGGTTCAC[A/C]CTGTCAAATGCACCA | 221178 |
rs374859607 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010117 | AGTGGGGAGGGGGCT[G/T]CCAGGTCATAGGTAG | 221178 |
rs374869739 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048990 | TATGAAAAGGAAATT[A/C]ATTGGGATAGGAACT | 221178 |
rs374871013 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189679 | TTATATATTATATAT[-/AA]ATTTATATATAATAT | 221178 |
rs374872160 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125569 | ACCAAGTGGTTTAAG[G/T]AGCGAGGGAGAATTA | 221178 |
rs374873186 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121292 | TCAAGTCACTATCAG[A/G]GGTGAGCGCACCACA | 221178 |
rs374874491 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24145941 | AGGGGGACGAGCACT[C/T]CCGACCAAGTCAACA | 221178 |
rs374877723 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133000 | CAAACAAACAAAAAC[A/G]AGTCTAGGAAAGGAA | 221178 |
rs374886193 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143217 | AGCCTGCAGACAAGG[A/C]GTCAGTGGGCAGGAA | 221178 |
rs374893332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186308 | GGTTTGGGAATAGCT[A/G]CAGGAAAATTGGATG | 221178 |
rs374916127 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169035 | TTCTAAAACAAATCT[A/G]AAATCCCCAGAGTGG | 221178 |
rs374923460 | in-del | -/ATA | 0.41325 | 0.18934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189788 | AAATATATTTATAAT[-/ATA]ATAAATATATATTTA | 221178 |
rs374975850 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185026 | GGCCGTCTTTGAAAG[A/G]CACGTGTATCGAGCA | 221178 |
rs374981631 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208399 | ATATAGATTGTGCCT[G/T]AGGAATATTGAAGTG | 221178 |
rs374984087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218636 | CAGTGGGCCGCAGGC[C/T]GCATGTGGCCCAGGG | 221178 |
rs375004610 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032639 | TTGGTTGAAAATAAG[G/T]CATTAGAGTTTCAGA | 221178 |
rs375009216 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052354 | GGTCAGGCTGAGCAG[C/T]GTTAACGAGATCCCA | 221178 |
rs375012642 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24214571 | ATAACAAAGCAATTC[A/G]AAGCAAAGAACCCTG | 221178 |
rs375024749 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104498 | TTTGTATATACCCAC[-/C]ATATGCAGGTATCTT | 221178 |
rs375031258 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092394 | TACTGCCTTGCTCTT[C/G]CATAGTTAGTGAATG | 221178 |
rs375032623 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029956 | CAAAGGACATGATCT[A/T]ATTCTTTTTTACGGC | 221178 |
rs375043806 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037697 | ACAGGCATGAGCCAC[C/T]GTGCCCAGCCGGCTA | 221178 |
rs375048655 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108660 | GCTGCTTTTCATGGT[-/A]GGGGGGGGGAAGCCT | 221178 |
rs375110569 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070090 | ATAGTTTAGCTTGGA[C/T]GGTGTTTCACATACT | 221178 |
rs375147843 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24197698 | AAATCAGTTAGACTG[A/G]CTTTGGTGTGATATT | 221178 |
rs375149589 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134797 | CTTCACTCGTTGTTA[C/T]GGACAGAATGTGTCC | 221178 |
rs375175727 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085040 | GTTCGCAGTCGCCTG[A/G]GATTCTGGGTTGGGG | 221178 |
rs375179593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122805 | TGTGGAGACTCTCGT[C/T]GTCATGTCAAACTGT | 221178 |
rs375187007 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135098 | AAACAGCCCTGCCAA[A/T]GCCTTGATCTCGAAC | 221178 |
rs375187255 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158873 | CCTCAAGGATGCGGG[A/G]GTCTTCAGGTCTAGT | 221178 |
rs375189328 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24055407 | TAGGCAAATATCTTA[A/G]TTTCTGTCTGCCTAG | 221178 |
rs375204400 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071735 | TTGTATTCTAAGTAA[-/G]GGCATTTAGTGAGGA | 221178 |
rs375226717 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015935 | TGAGCATCAAAGACA[C/T]GCTTCTGTCCTTCGT | 221178 |
rs375234139 | snp | A/T | 9.97291e-05 | 0.00706078 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286929 | GCGGGTGTACATCAA[A/T]CACCTCAGGGACATC | 221178 |
rs375258043 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116977 | AGAGTACTGACCAGG[A/G]ACTTAATCAGAGGGC | 221178 |
rs375272174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080608 | CGCACACCACCTAAG[A/G]AGGTAACTTCCCCTT | 221178 |
rs375286426 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291740 | TCTCTCTCTGTCTTT[A/T]TTTTTTTATTTTTTT | 221178 |
rs375303028 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24264295 | AAGAAGAAGAAAGAA[C/T]ATTAAAAGTCAGAGG | 221178 |
rs375306122 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026664 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG | 221178 |
rs375319934 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24292535 | GGTCATCTCAAAGGG[C/T]CCTAATGAGAAGAGG | 221178 |
rs375325149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212724 | GAAACACATGCCTGC[A/G]CAGTCACTTTGCCAG | 221178 |
rs375328785 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24294662 | CGTATACGAAGAAGC[A/G]CCCCAGTGGATTATT | 221178 |
rs375332036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123224 | TTTTTCTTGATTGCT[C/G]ATCAATACTTGAAGG | 221178 |
rs375341755 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108774 | CGAGCCCACAGTTCC[C/T]TGGGATTTTTCGGAA | 221178 |
rs375346622 | snp | C/T | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223010 | CCTCGGGCCAGGCCC[C/T]GCAGCCCCCTGTGCA | 221178 |
rs375348354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027440 | GCCTGGCTGCCTTTT[C/G]TTTTTTTTTCAAACT | 221178 |
rs375353324 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293792 | TGAAGACAGCAGGGT[C/T]TGCTTGGTGGGCAGT | 221178 |
rs375366478 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24267446 | ATCCCAAGGATGTTA[A/G]TCTAGTGCCCTGACC | 221178 |
rs375379459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233417 | ATCTGAAGAGAATTA[A/T]TGTGCCTTCTATGAG | 221178 |
rs375380167 | snp | A/G | 0.000875616 | 0.0209055 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217336 | TTCTTCTTCCTAATA[A/G]CATCAGTGGCCACAG | 221178 |
rs375381936 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013140 | CAGACATGGAAAAAC[C/G]TCAGCCTCCTCTTCT | 221178 |
rs375385282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217139 | TGGTATGTACCTGTT[A/G]TCCCAGCTACTTGGA | 221178 |
rs375396354 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057069 | TTTCTTTTTTTTTTT[C/T]CTTTTTTTAAAAAAT | 221178 |
rs375401395 | in-del | -/CCTCCCTCCCTCCCTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278981 | CTCCTTCCCTCCCTC[-/CCTCCCTCCCTCCCTT]CCTTCCTTCCTTCCC | 221178 |
rs375402659 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022034 | GAAAATCTTAATGTT[C/T]CTTTTCTCTTTTCTT | 221178 |
rs375403006 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135693 | ACAGAGCAAGAATCC[A/G]TCTCAAAAAAAAAAA | 221178 |
rs375410951 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117693 | TTAAGAGAAAAAAAA[A/C]CCCAAACTCATTCCT | 221178 |
rs375415791 | snp | A/G | 1.76886e-05 | 0.00297389 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300381 | TTCTGAATATATATC[A/G]CATTTATTTCTAAAT | 221178 |
rs375428551 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174044 | GAATTGGTGTTAATT[A/C]TTTTTAAGCATTTGG | 221178 |
rs375443072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263580 | ATCCTCCATATACTT[C/T]AAATCACCTCTAGAT | 221178 |
rs375445523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272203 | AGGTGGCCCCTGGCT[C/T]TCCTCCAGCATTCCT | 221178 |
rs375454725 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001734 | ATATGGAGGGAAATG[A/G]AGAAAGAGAACCTGA | 221178 |
rs375462276 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307415 | TGAAGGCTAGGCCCT[A/G]CCACAGGAGCTGTGC | 221178 |
rs375468247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021336 | AAGATGATTAAGAGA[A/C]TATCAGGCATAGGGC | 221178 |
rs375471736 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063200 | ACAGCCAGAACCTGG[A/T]TTTATTCGCGTCTGC | 221178 |
rs375478890 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24087000 | CCCAAAGTATTAGGA[A/T]CGTTTTCTTTTTTTA | 221178 |
rs375488101 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108036 | CCAAGATCAGGGCAC[G/T]GGTAGGCTCGGTGTC | 221178 |
rs375493378 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022856 | AGAAAAAGAAACATT[-/T]GAATCATGAGCTGGA | 221178 |
rs375499104 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24096601 | GTCTAAAAAAAATAA[C/T]AATAACAAGGGGGAC | 221178 |
rs375500284 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SPATA13 | GRCh38.p7 | 13:24290724 | GAGCTCGCCAACCTC[A/G]TGAAGCAGGGCAAGT | 221178 |
rs375504758 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015750 | GCAGGCCCCCCCCCA[A/T]TTCCTAGGTCCACCG | 221178 |
rs375509470 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24106688 | CAGAGCTGGCTCTCG[A/T]TCCAGGGCAAACTTA | 221178 |
rs375509502 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24176132 | ACAAAGGTAGAGTCC[A/G]AGTGTAAATTTCTCA | 221178 |
rs375522737 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064774 | CAGCGATGAAGGTCA[A/G]TACCACCACTGATGT | 221178 |
rs375530663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103830 | TTCCAGAGAATTTTC[A/G]TCCCTTTCAGAGTTA | 221178 |
rs375533406 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213244 | ACACAGTACCCACTT[C/T]GGAACACTGCAAAGG | 221178 |
rs375535108 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025925 | TTCTCCTGCATCAGC[A/C]TCCTGAGTAGCTGGG | 221178 |
rs375540443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166755 | GAGCATATGCTTCCT[A/G]GAGGCTCTGAACAGC | 221178 |
rs375542116 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082813 | GCCTGGGCGACAGAG[A/C]GAGACTCCGTCTCAA | 221178 |
rs375559979 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044617 | ACATTGTTTAATGAT[C/T]GAATCGGGGTAATTA | 221178 |
rs375562581 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011059 | ATATGCCTGCACTCT[G/T]CAGTTTGCTGACTCC | 221178 |
rs375566421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133940 | GGGTTTCGTGAGCAA[C/T]GCTTCATGTATCCTG | 221178 |
rs375569975 | snp | G/T | 0.000153988 | 0.00877328 | missense | SPATA13 | GRCh38.p7 | 13:24289124 | AGACCTTGAGAAACA[G/T]TACAACAAAGAGGAA | 221178 |
rs375577567 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288956 | CTATTCAAATAATTT[A/G]TTTGGATTTCCAAAT | 221178 |
rs375611001 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036520 | GAACAGACACCTGAA[C/T]GTTCTTTAGGTGACT | 221178 |
rs375612710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170010 | TTCATACAAAGTTCT[C/T]ATCCCTAGAGAGTTC | 221178 |
rs375614621 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193914 | AGTAATTGGGATTTT[A/C]ACACATTGTGATGAG | 221178 |
rs375641139 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118500 | GCACATGTCAGATGT[A/G]GCTCATTCATTCCAA | 221178 |
rs375655074 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140924 | CTCACGCCTGTAACG[C/T]CAGCACTTTGGGATT | 221178 |
rs375663927 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098650 | GAAAAAAGAAAGGGC[C/T]GGATGTGGTGGTTTA | 221178 |
rs375664061 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24152684 | GGAAGATGTCTCTCT[C/G]TGTCACTCACCATCA | 221178 |
rs375668348 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24251948 | CAGCAGGTTCTGCAC[C/T]TTCGCGCCTCCCTTG | 221178 |
rs375678578 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070822 | CGTCTGGTTTTTTTC[C/T]GCCTTCCGACTCAAA | 221178 |
rs375687070 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110303 | GGGAGGGGAGGATGG[C/T]TCTACCTCAGACCTC | 221178 |
rs375704888 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24055922 | GGCGTTGGCAATGCC[A/G]TGCCTTTTTATGGAA | 221178 |
rs375710923 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24093924 | AACTGTAATCAGACT[A/G]TATACCTCAGGCCTC | 221178 |
rs375713317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211675 | CAGGCCATGTTGACT[C/T]TCTCCCCATCACCTC | 221178 |
rs375716604 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24131063 | TAAAGGACAAGGATT[A/G]TTCAGTAAGGAAATT | 221178 |
rs375733017 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167043 | TACATTGGTGCCTAC[G/T]CTTACCTTCAAATGT | 221178 |
rs375747090 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24094787 | AAAAATTAATATGTA[A/C]AATATTTCAGAATAA | 221178 |
rs375761429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140568 | TCCCTACAGAGTCAA[A/G]CGTTCCTCTTCAAAG | 221178 |
rs375779178 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128253 | GACATTGTCCTTGTG[C/G]CCGGAGGGGTGACCT | 221178 |
rs375792773 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128462 | GAAGAGAAGGGTGTT[G/T]CTCAGAGGTAATTAA | 221178 |
rs375793875 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159312 | AAAATACATGGTCAT[C/T]GTTAAAACTTGGGGT | 221178 |
rs375794152 | snp | C/T | | | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307289 | CCCTGGCTTGAGAAA[C/T]GTCAGTGGTTGGAGT | 221178 |
rs375797243 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135409 | CACTCTTTAAGAGTA[A/T]TTTTAGGTCCAGGTG | 221178 |
rs375801916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079117 | GTAGGAGGCAGTGGC[A/G]GAAGGGAAGAGGGGG | 221178 |
rs375804682 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116387 | TGCCATCCTCCAAGA[C/T]GGGAGACACAGAATT | 221178 |
rs375825240 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24234550 | CATGATGGTGATGAT[G/T]AGAAGGAATGCCGTA | 221178 |
rs375827234 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211657 | TGTTGTCCAGCTGGT[C/T]AGCAGGCCATGTTGA | 221178 |
rs375832060 | snp | A/T | 1.65231e-05 | 0.00287424 | missense | SPATA13 | GRCh38.p7 | 13:24251814 | TCCCAGAGCACCCCC[A/T]TTGGGTTGGACCGTG | 221178 |
rs375836298 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112490 | AGAGTTGAATTCTCA[A/T]GCTCAGCCACGGAAG | 221178 |
rs375838873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021230 | GGAGTTGACAGAGAA[C/T]GGGGAGTATTCCAAG | 221178 |
rs375839910 | snp | C/T | 1.65564e-05 | 0.00287714 | missense | SPATA13 | GRCh38.p7 | 13:24290839 | AGATCTGCAAATACC[C/T]GCTGCAGCTGGCCGA | 221178 |
rs375841697 | in-del | -/T | 0.0788843 | 0.182262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202963 | GGAATTATGGTGAGA[-/T]TTTTTTTTTCCCTCA | 221178 |
rs375859526 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126206 | AGGATGAAGTCATGG[A/G]GGCAGGAGCCATGGG | 221178 |
rs375862336 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23991552 | ATGCTGCAAAGTTAG[C/T]GAGCCCCGGCCCGCA | 221178 |
rs375865726 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24093792 | GGGAAAAGATCTAGG[A/C]TGTGGTCATAATACT | 221178 |
rs375868042 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006898 | GGCAATTAACACGAA[A/G]CCCCTCTCTGGAAGG | 221178 |
rs375868647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104117 | GAGCTGTAGATGACA[C/T]GTTTGAGAATGTCCG | 221178 |
rs375880641 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189682 | ATATATTATATATAT[A/G/T]TATATATAATATATA | 221178 |
rs375908610 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980331 | CGAGCCGCAGCGTGG[C/T]TGTGTTGCCGGGCGA | 221178 |
rs375929715 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074796 | CTGTTAGCCAGCCAG[A/G]ATAGGTTTGGAGCAA | 221178 |
rs375933961 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174553 | CAGTTAAATATATGA[C/T]TAAAAATTTCCCTTT | 221178 |
rs375947610 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24008469 | CACCATGAAAGAGGG[C/G]GGTGCCCCCAGCCCC | 221178 |
rs375964696 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24279349 | TGTATCTGGGGAGAG[A/G]TCTCAAGAACTTTGG | 221178 |
rs375973048 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24265012 | TGGTTTTGTGTGTTC[A/C]GGTCCACATTGCTCC | 221178 |
rs375988793 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24249328 | TTGGTTGTGTCTTCA[C/T]GTTCTAGTACACAAA | 221178 |
rs375993460 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168312 | GTCCTGGTAAGGTGG[A/T]TGAATTAATGACATA | 221178 |
rs376019565 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101982 | CCTTGCTTTTAGTTC[C/T]TTTGGATATATACCC | 221178 |
rs376064468 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293647 | AGTTTTGTCCAGAAA[A/G]ACTTATTTTGCGACC | 221178 |
rs376066669 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23985835 | AAGTGCTGGTCACAA[A/C]CCTAGATGGTGACTG | 221178 |
rs376078243 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001905 | GCTGGAGTGTGGCTG[G/T]GGGAAGGATGGTGAG | 221178 |
rs376082649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246723 | TCTAAATTAGCTGGG[C/T]GTGGTGGTAGGTGCC | 221178 |
rs376088972 | snp | C/G | 1.65828e-05 | 0.00287943 | missense | SPATA13 | GRCh38.p7 | 13:24286250 | GTCTGCGCAGAAGCC[C/G]TGTGGGACCATGTGA | 221178 |
rs376092898 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198262 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 221178 |
rs376101325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030636 | GTCTGAGTATTCAAC[A/C]ATCTCTTATTTCCCT | 221178 |
rs376117752 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291202 | TGTCTTTGAGTACTC[A/C]GTAGTTAGTAAAGAC | 221178 |
rs376120974 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276748 | AGCTTTACAGCGTCA[A/G]AATTCCCTTAGATAA | 221178 |
rs376121387 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996531 | ACCTAAGAAAATGAA[A/G]TGATGTGCAGAAACA | 221178 |
rs376121849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277250 | GAGATCGAGACCATC[C/T]TGGCTAACATGGTGA | 221178 |
rs376123663 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258998 | GCATCCTTGGGGTGG[A/C]CCATCCATATGGGTA | 221178 |
rs376129935 | snp | C/T | 6.62482e-05 | 0.00575497 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24249710 | AAGCATGACTTCTGC[C/T]AGCCCTGAAGACCAG | 221178 |
rs376143758 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983618 | AATAGTGGCCATTTA[G/T]TTTTACACTAGTATA | 221178 |
rs376147192 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23985030 | TTTAATCAAAATGCT[C/T]ACCTCAGACGCACCC | 221178 |
rs376166804 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085143 | CCCTTGTTTTGTTGA[A/G]ACAGATTCTTGCTCT | 221178 |
rs376184128 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227333 | GTTAAGTGAATATAT[A/G]TGAACTAGTGTGTAG | 221178 |
rs376204088 | snp | A/C | 0.0614824 | 0.164198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112337 | ACTCTGCTCTTGTTG[A/C]CCCTACAGCACCTTC | 221178 |
rs376208272 | snp | A/G | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224525 | TGATGAGGGCAGCAA[A/G]GACCTTCTGGTGAAC | 221178 |
rs376209869 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206872 | CTCCAGCCTGGGCAA[-/AA]CRAGWGAAGCTCTGT | 221178 |
rs376213739 | in-del | -/TGTGTGTGTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173363 | TCATTAGTTCTTAGT[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 221178 |
rs376220299 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305486 | GGGTTTTATTACCAC[A/G]TGCCTGAGTTCTTCA | 221178 |
rs376238402 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087027 | TTTAATAAAGCAGAA[C/G]AGCAATTGTGGAGAA | 221178 |
rs376254629 | snp | A/C/G/T | 9.88871e-05 | 0.00703105 | missense | SPATA13 | GRCh38.p7 | 13:24302760 | TCAACAGGCTCACCC[A/C/G/T]CTTCCGGAAATGAAA | 221178 |
rs376269064 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285630 | CAAGCAATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 221178 |
rs376321430 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24022479 | CTTTAAAATTTTAAA[A/G]TAATGTTTAATGAGT | 221178 |
rs376348954 | snp | C/T | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223673 | AAACAACAGCATGGG[C/T]TACAGGAGGAGCAAG | 221178 |
rs376357066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194982 | AATACCAGTTCACCA[A/G]TGATTTCTAATTCAA | 221178 |
rs376364119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062453 | AGGGTGCACGGTGCT[A/G]GGAGCCAAGGGGCTC | 221178 |
rs376375893 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110128 | TAGGGTAAATAATGG[A/C]ACTTTGTTTCTTTAC | 221178 |
rs376384873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078739 | AATAGCCCATCAGTG[A/T]ACATTCACCTTCCCA | 221178 |
rs376385928 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154910 | TTGCCCAGGCTGGAG[G/T]GCAATAGCATGATCT | 221178 |
rs376403950 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100821 | TGCATTTCACTGCAC[A/G]TCTTCATCCAAGCTT | 221178 |
rs376422802 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24225038 | CCTAATGTCACAGCA[C/T]CTGTGGGTGTCACTT | 221178 |
rs376426755 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206232 | CAAATTTACAAGAAA[A/G]AAACAACACCATTAA | 221178 |
rs376427401 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24244729 | ATTAGCTGGTGTGGT[A/G]GTATGCACCTGTAGT | 221178 |
rs376440738 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098618 | AAAAAAGAAGAAGAA[A/G]AAAAGAAAGAAAGAA | 221178 |
rs376441903 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248377 | TGCCTGAGATTGCAC[A/T]AGGTCTTGGGCCAGA | 221178 |
rs376443899 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011399 | GGGATCCCTGAGACC[A/G]TTCTGGGCAGGTCTG | 221178 |
rs376443943 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042446 | TGCTTCTGTTTCCAA[A/T]GCAAACCAGGCTGCT | 221178 |
rs376449176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240413 | ACAATTATCATGAAG[C/G]CTAAGGGGGAAAAAC | 221178 |
rs376475147 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262316 | TTTTTTTTCTTTTTT[C/T]TTTTTTAGCTCTTTT | 221178 |
rs376475254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181591 | CATTAGCCTAGGTCT[A/G]CATAGGGTCAGCATC | 221178 |
rs376481427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092996 | AGGATCACCAAAGGC[C/T]GTGATGATTAATCTT | 221178 |
rs376486791 | snp | A/T | 0.000423594 | 0.0145471 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24222973 | CACCCTGCCTGGAGA[A/T]CATGACCACTGCCCC | 221178 |
rs376488888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193429 | GAGCAGATGCCTCAG[C/T]GTGGTTGAATCTGAG | 221178 |
rs376494738 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102087 | AGCTGCACCATTTTA[C/T]ATTCCCACTAACAGC | 221178 |
rs376502698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120379 | CTGTGTTGCTTTTCT[C/T]TGGGGAAGATGTATG | 221178 |
rs376504998 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119679 | ATCTGTGTCTTCTAA[C/T]TTAGCAAAAGAATCT | 221178 |
rs376505603 | snp | C/T | 0.000912159 | 0.0213365 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223643 | CGTGTGTGAGATTCT[C/T]GTGAGGGACCCTGAA | 221178 |
rs376517073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169303 | GTGAGGTGCTAACCC[C/T]GGAAAGCTCCCCTTG | 221178 |
rs376552085 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24079487 | AGACTCTGGCTGAAC[G/T]TTCCCTGCTACCTGG | 221178 |
rs376552329 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146742 | ATATACCTTTGTGTC[G/T]AAAGCATTTTCCATC | 221178 |
rs376554564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070160 | GATTGTGGACTAAAA[C/T]GGTTCCAGTGTCAGA | 221178 |
rs376558445 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24177632 | GCCTAGCTAATTTTT[C/T]AAATTTTCTGTAGAG | 221178 |
rs376569772 | snp | A/T | 0.334412 | 0.235318 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190067 | CATATAATGATATAC[A/T]ATATATATTATTATA | 221178 |
rs376573029 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174696 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 221178 |
rs376576960 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24235293 | TATCAGCAATCAACT[C/T]GGGAAAATGACTTTT | 221178 |
rs376585686 | in-del | -/CAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217069 | AACAAAACAAACAAA[-/CAAA]AACAAAAACAAAAAA | 221178 |
rs376587072 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24130472 | AGATAAAGGCAAAGC[A/G]TGGTTGATGAGAACT | 221178 |
rs376588355 | in-del | -/GTA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24122642 | CTTTTTGCACATACT[-/GTA]TATCACTTCAAGATA | 221178 |
rs376599180 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24131390 | CAGGGCTGACTCACA[A/G]AACCATCTACCCGAA | 221178 |
rs376601649 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276967 | AACTGCAAATTGCTA[A/T]TTCCCCATCAGCAAT | 221178 |
rs376603311 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172959 | CTCTTCATTTATTTT[A/G]TCTTTTTTGATTAGT | 221178 |
rs376626648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198192 | TAGAGACGGGGTTTC[A/G]CTGTGTTGGCCAGGC | 221178 |
rs376630392 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082648 | ACAAGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 221178 |
rs376632397 | in-del | -/TT/TTA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291747 | TGTCTTTATTTTTTT[-/TT/TTA]ATTTTTTTATTTTTT | 221178 |
rs376664577 | in-del | -/TTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24191499 | TCACTATACATTGCT[-/TTC]TTTTTTTTTTTTTTT | 221178 |
rs376665951 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125472 | TTCCACACCTCCTTC[A/T]GCATACAGAATACAC | 221178 |
rs376689970 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019075 | CTAAGTTATATGATT[A/C]TTATTATTATTATTA | 221178 |
rs376690777 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293515 | GGCATTTTTCACCAA[C/G]AGCATTTGCAGATTT | 221178 |
rs376697326 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24111708 | GCCATGCCCGGCCTG[C/T]GTCCATATTTTAATG | 221178 |
rs376716749 | snp | C/T | 0.000142946 | 0.00845298 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284303 | CGACAGTAGTGGATA[C/T]GGGATACCTGATTTT | 221178 |
rs376719918 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980345 | GCTGTGTTGCCGGGC[G/T]ACGGAGGAGCCGCGG | 221178 |
rs376758893 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138231 | AGAATTGCTTGAACC[C/T]AGAAGGCAGAGGTTG | 221178 |
rs376764814 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24120252 | CTAGTAAATGGTTAT[C/T]GAGAAATTGGAGTGT | 221178 |
rs376765042 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037403 | GTTCTCGACTAATAC[A/T]TTATTTATTTATTTA | 221178 |
rs376778076 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018622 | AGGCACAGCTAATTG[A/G]CGAGGTGAGCGCTGC | 221178 |
rs376780083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283139 | CGCACTGTTCTGAGT[C/T]GCCTGCTCCTCTTCC | 221178 |
rs376781130 | snp | A/C | 0.0126979 | 0.078662 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305872 | CTGCCGTAGATTAAA[A/C]GCAATTATAAAATCA | 221178 |
rs376784717 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228946 | CAGTCTAACAAGATT[G/T]TGTATTGCTGTGAAA | 221178 |
rs376790087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254933 | ATGATTGATTAGCCT[C/T]TCTTGCAATAAGGAT | 221178 |
rs376797675 | snp | C/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979141 | TTTAACAATTGATTA[C/T]CTTGGGATATAATTA | 221178 |
rs376818449 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084203 | AAAGCAGCTGAACAA[C/T]TTAAATGCGTTGGGG | 221178 |
rs376845707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154152 | CTTGGCCGTAGCTAC[A/G]GAAGGTAAACATATG | 221178 |
rs376848220 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189921 | ATTACATAATATATA[A/T]TATATAATTATATAA | 221178 |
rs376852922 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041887 | CTTTGCAAAGAGCAG[A/G]TGGAATCAGAGTGAG | 221178 |
rs376881335 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24270993 | GTTGCAGTTCTTCCC[-/CT]CTCTCTCTCTCTCTC | 221178 |
rs376883778 | snp | A/G | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303068 | TAAAGCGAGTGATTA[A/G]GCAGCAGCTGAAGCC | 221178 |
rs376901200 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24215862 | CTGGAAAATTTTCAT[A/T]GCCCTGAATGGTAAA | 221178 |
rs376910091 | snp | A/C | | | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252640 | TACCTGTGTACACAC[A/C]GCCTTTCCCTGCTTT | 221178 |
rs376912782 | snp | A/G | 0.000168708 | 0.00918289 | missense | SPATA13 | GRCh38.p7 | 13:24284231 | GCCAGGCCAGCCCTC[A/G]GTACCTGCAGCCCGG | 221178 |
rs376923035 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253949 | GAGGAGGCTGAGCTT[G/T]TTCTAAGTGTGGTGT | 221178 |
rs376933201 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24190944 | GAGTCAACAAATGCA[G/T]CAAACCTCACTGTCT | 221178 |
rs376944515 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24234478 | GATCAAAGGCCACCC[A/G]GGGTGGAATTGCTTT | 221178 |
rs376948589 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063775 | GAAACCTGCTCTCTA[C/T]GGCACATGTCATCCA | 221178 |
rs376950306 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270284 | CCTTTACATGTATGC[C/T]TTTACATGTATACCT | 221178 |
rs376953910 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052828 | TTCCCCCTGCCGCCA[C/G]GGGATCCTCCCCGCC | 221178 |
rs376960178 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24032216 | TCCCTCTTAGTGATT[G/T]TCTGTCCACTGACTC | 221178 |
rs376961900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057151 | TTTGTTACATATGTA[C/T]ACATGTGCCATGCTG | 221178 |
rs376968984 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24020535 | TGTTGAACCTTAAAC[A/G]AATTGTATTTAACCT | 221178 |
rs376973419 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24095830 | TCAGCTGTAAAAACC[A/G]TCATTTCTATCTATG | 221178 |
rs376976418 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156083 | TTTATTCATCCATCC[A/T]TTGATGAATACTTGG | 221178 |
rs376991381 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172497 | GGTTTTTCATTTTAC[A/G]GTTAAGTCCATGATC | 221178 |
rs376992101 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24274076 | AGAGGTCAGCGTGGA[C/T]GGATGGAAGGATTTT | 221178 |
rs376997222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253716 | CTCTCCAAGGAGGTG[A/G]CGCTGGGGACAGGTG | 221178 |
rs377014791 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216015 | ACAGGCCATGGCTGT[A/G]GGAAGTCAAGACGCA | 221178 |
rs377018071 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225405 | GGGGAACGTGGTGAC[A/G]AGTGAAAGCTCAGAG | 221178 |
rs377037699 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284951 | TGGCAGAGCTGGAGG[C/T]ACCCATGTATTTCTC | 221178 |
rs377038065 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24301677 | CCTTCTGGCAGGCCA[A/G]GGGCAGGGACGGGTT | 221178 |
rs377038249 | snp | C/T | 8.25307e-05 | 0.00642328 | missense | SPATA13 | GRCh38.p7 | 13:24251784 | GTGTCGGCCCGGTTC[C/T]GGCCCTTCACATTCT | 221178 |
rs377038701 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173499 | CGCCTTTTATTCCCC[A/C]CCGTCCCCCAACTTT | 221178 |
rs377041784 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282896 | CAGAATTCAGACGAG[A/T]CTCTGTGACCCTAAA | 221178 |
rs377072516 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24240177 | AAGCAGAAGGATCAC[C/T]TGAACCCTGAAGGTT | 221178 |
rs377075297 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038820 | TAATAAGGAAGCACA[A/G]CATCAAAAAATTGGG | 221178 |
rs377093885 | snp | C/G | 0.000153988 | 0.00877327 | missense | SPATA13 | GRCh38.p7 | 13:24249825 | CAGACGGAGGAACTG[C/G]ACAATCTTCTGACCC | 221178 |
rs377098623 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299695 | TCTGCCAAGCTGGAG[C/T]GAGTACCTGCCTACA | 221178 |
rs377098985 | in-del | -/GCCTTTACATGTAT | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270295 | TGCCTTTACATGTAT[-/GCCTTTACATGTAT]ACCTTTTGAACAAAA | 221178 |
rs377107566 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271021 | TCTCCACTCTCTCTC[A/T]CTCTCTCTCTCTCTC | 221178 |
rs377121531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212280 | AACCTGGGTGACAGA[A/G]TGAGACCCTGTTTAA | 221178 |
rs377129163 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242346 | CCAGAGAAATACATA[C/G]AGCAGAAGCCAGCAG | 221178 |
rs377132019 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24088866 | CCAAGGCTGGCTCCA[C/G]GAAAGCGCAAGCAAG | 221178 |
rs377151248 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242776 | CTGCATATGTAAATA[A/T]TTCCTTGTTCCTGCT | 221178 |
rs377160791 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24194070 | CATGGTTCAGTAGCC[A/G]AGTCTGTGGTGGGCA | 221178 |
rs377167057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203234 | AGTTGTCTCTTCCCC[A/C]GTGCCCTCTTTGTAA | 221178 |
rs377167389 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216234 | TCTCTCACTACACCA[G/T]CCTGACCTGCAACTT | 221178 |
rs377168301 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212210 | TTGAGGCCAGGAGTT[A/C]AGGGCTGTGGGGAGC | 221178 |
rs377171688 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278400 | AATCAGTGCCTAGCA[C/T]ATTATAGGCACCTGA | 221178 |
rs377174085 | snp | A/C/G | 9.57258e-05 | 0.00691764 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223098 | TGTGGCTGCAGCCCT[A/C/G]GTGGCGACACGGACA | 221178 |
rs377184614 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027135 | TTTTTGTTTAGCCGT[-/TT]TTTTTTTTTTTTTTT | 221178 |
rs377188360 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102723 | AGGTGATCCACCCAC[C/T]TCAGCCTCCCAAACT | 221178 |
rs377191587 | snp | A/C | | | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033721 | TTGCGTAGTGTGCTG[A/C]TGGAGCAGTTGCCTC | 221178 |
rs377201059 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057083 | TTCTTTTTTTAAAAA[A/T]TTTTATTATTATTAC | 221178 |
rs377238152 | in-del | -/GA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103526 | AAAAGAGCAGGGGAG[-/GA]GAGAGAGAGAGAGAG | 221178 |
rs377241047 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054605 | CAAAACACAAACTCT[-/T]AAGAACTTTTAAAAT | 221178 |
rs377269650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003074 | ATTGACTCAGTCTTC[C/T]GAACTACAGCATTTG | 221178 |
rs377270649 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220590 | ATCCAGTCTCATCGC[A/G]GAGATGATTCAAGCC | 221178 |
rs377276017 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24075913 | TATAGAAGAAATAAT[A/T]TCTGCAGAAGAATTA | 221178 |
rs377304095 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24049243 | GTCACTGATGCCTCG[C/T]CTACAGGACAGCAGC | 221178 |
rs377304860 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189651 | TATTTATATATATAT[A/T]ATATATTATATATTT | 221178 |
rs377320635 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24012063 | TCTTGCAGCCATTGT[A/G]TCTGACCATGGGCCC | 221178 |
rs377323179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279022 | TTCCCTGCCTCCCAT[A/G]TATGCCAGGCAGGAA | 221178 |
rs377324848 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301058 | CTGATGCCCAGGCCG[A/C]ATACCCAGGGGCTCT | 221178 |
rs377330138 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24284784 | GCAGCTCCCCATCAG[C/T]GTTCGGCCAGTGCTT | 221178 |
rs377345003 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062370 | AGGCCAGGGACTGAC[C/T]GGGGGCTGATCAGGA | 221178 |
rs377347689 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24249166 | TGAGCCACCGCATCC[A/G]GCCAGTGCTGATTTT | 221178 |
rs377364615 | snp | C/T | 0.000437904 | 0.0147905 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223693 | GGAGGAGCAAGAGCA[C/T]GGACAATCTTGCCTT | 221178 |
rs377368045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169955 | GGAGAAAGCAAGAAC[C/T]CTCCCTGCTTTTTCT | 221178 |
rs377378079 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169398 | GGCAGCTTCTTCCGA[A/C]CATTTTATTTTTTCA | 221178 |
rs377404181 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077980 | TGAGGACCTTCAAGG[A/C]TTGGCCTGCGATTGT | 221178 |
rs377416068 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24141597 | ACAATCACTAGGGCA[A/G]TCCCTGTGATAACAT | 221178 |
rs377424038 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24153379 | CAGCACACTCTTCTC[A/G]CACTCCATTTCATTG | 221178 |
rs377426164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035989 | ACTGCACTCCATCCT[G/T]GGTGACAGAGTAAGA | 221178 |
rs377431841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016534 | GGTGCCCTTCTTTGC[C/G]CACAGCCAAGCAGGG | 221178 |
rs377435847 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008931 | CTCTGGGACCAAGTG[C/T]GGGAGGTGGGGGCTG | 221178 |
rs377435969 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268981 | TAGTATATAGTCAAC[-/AT]GTGTGTTATTACTAA | 221178 |
rs377437327 | snp | C/T | 5.37658e-05 | 0.0051846 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286409 | GTAAGTGTGGGGTGC[C/T]TGCAGCTTTTCCAAA | 221178 |
rs377458724 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057709 | TTTTGGAATTGCCAC[A/G]CCGTATATATGTGTG | 221178 |
rs377468417 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031590 | TGAAATGAACATTTT[A/T]AATAACTGAGATTTC | 221178 |
rs377469353 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998473 | TGCTCTGGATAAAAG[A/G]TCTTTATCAGATATG | 221178 |
rs377482418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144077 | CTGTGAATGTTCATG[A/G]GCTGAATGTGCACTA | 221178 |
rs377493795 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172655 | TCTTTATCAAAAATT[A/T]GTTGGTTTTATTTGT | 221178 |
rs377501268 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230211 | GCATAAGGAATTGTC[A/T]TGTACCTCACCACTC | 221178 |
rs377511005 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092253 | AAGTTAGGAAACAAT[A/G]ATCATGTGATGTTTT | 221178 |
rs377538715 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24268338 | GTCTGCTGTGAAAAA[-/A]CAGTATCGAGGAGTC | 221178 |
rs377557799 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285136 | ATGTGTATCGTTGGG[C/T]GCTAAGGAGATGGGC | 221178 |
rs377578835 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24281113 | CCAGGCCCTGCCATG[C/G]CCCTGGCAACCGTCC | 221178 |
rs377582198 | snp | C/T | | | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252714 | TTAGCGTTCTTTTGT[C/T]GAAAAGCAACAAAAC | 221178 |
rs377585181 | in-del | -/CAGTAGAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24300582 | TTGGAGCAAGGAGAA[-/CAGTAGAA]GTTAGAACTCAAGGG | 221178 |
rs377611811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173139 | CTGGAGTGCAGTGGT[A/G]CGATCTTGGCTCACT | 221178 |
rs377652445 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115073 | CTTGTTTGCCGTATA[A/T]GCTCCTGCAGAGAAG | 221178 |
rs377695443 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24261285 | CAGGGAGCAGCCATC[C/T]GTGCTGCCTCTGATG | 221178 |
rs377705777 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025197 | TCCTATTTTTGTTTA[C/T]TTCCTAAAATTTTTA | 221178 |
rs377717449 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248805 | ATTACCCATTCATTT[C/T]TTCTCCTGGCAGGTC | 221178 |
rs377723424 | snp | A/G | 1.90947e-05 | 0.00308982 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297785 | TCTGCTTGCTGTAAT[A/G]GCTTCATTCTCCACT | 221178 |
rs377725402 | in-del | -/ACTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980624 | TTTTGAGACAGTCTT[-/ACTT]TGTCGCCCAGGTTGG | 221178 |
rs377727753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251938 | TAACCTGAGGCAGCA[C/G]GTTCTGCACCTTCGC | 221178 |
rs377735779 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181775 | ACTTTTTTTTTTTTT[G/T]TTAAAGTAAGTAAGT | 221178 |
rs386363426 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142111 | ATTTGTAGGGAAAGG[-/TT]TTTTTTTTTTAGCTT | 221178 |
rs386378479 | in-del | -/CATACT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23995226 | TTAAAATTATTTATC[-/CATACT]ATACTTAGCTGATCT | 221178 |
rs386378480 | in-del | -/GAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996618 | ACCTGTGCTTGGCTG[-/GAT]ATTGGCTGAGATTTG | 221178 |
rs386378481 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24019104 | ATTATTTTTTTTTTT[-/TTT]TTGAGACGGAGTCTC | 221178 |
rs386378483 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24027151 | TTTTTTTTTTTTTTT[-/TT]TGAGACGGAGTCTAG | 221178 |
rs386378485 | in-del | -/TCATGATG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074499 | ACATTTAATTGTACT[-/TCATGATG]CATGATGACTGTCCC | 221178 |
rs386378486 | in-del | -/AGTAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24086068 | AGTTTCACTGTGGGA[-/AGTAG]GTAGCAGGAGAAAGC | 221178 |
rs386378488 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181762 | GTTTTACAGTTGACT[-/TTT]TTTTTTTTTTTTGTT | 221178 |
rs386378489 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181772 | TGACTTTTTTTTTTT[-/TTT]TTGTTAAAGTAAGTA | 221178 |
rs386378492 | in-del | -/GTTTCTCTGAGAGGGGCACCCCAGGCAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24281638 | GCTGGGATGTCGGGG[-/GTTTCTCTGAGAGGGGCACCCCAGGCAG]TTTCTCTGAGAGGGG | 221178 |
rs386378493 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291765 | TTTTTATTTTTTTTT[-/TTT]TTGAGACGGAGTCTC | 221178 |
rs386419843 | in-del | -/C | 0.0759472 | 0.179459 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057029 | TCTCTCTCTCTCTCT[-/C]TCTTTCTTTCATAGC | 221178 |
rs386768988 | multinucleotide-polymorphism | CC/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980872 | GCTGGGATTAGAAGC[CC/TT]GAGCCACTGCGCCTG | 221178 |
rs386768989 | in-del | CCTTTCC/GCATTGCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997550 | ATATTAGTCCATTTT[CCTTTCC/GCATTGCT]ATAGAGAAATACCTG | 221178 |
rs386768990 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003876 | CACAATATACATCAG[CA/TG]AATACAGAACCCATT | 221178 |
rs386768991 | multinucleotide-polymorphism | GCG/TCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003971 | TTTTGTACACTTGCT[GCG/TCA]TATACATACACACAG | 221178 |
rs386768992 | multinucleotide-polymorphism | GC/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24007198 | CCTGGTGGCCCTGAG[GC/TT]TCTGAGCCCTCTGCA | 221178 |
rs386768993 | multinucleotide-polymorphism | GGTATA/TGTATG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029508 | ACAATAAAAAAATTT[GGTATA/TGTATG]TTATTTACATAAAAT | 221178 |
rs386768994 | multinucleotide-polymorphism | CT/TC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24033422 | ATGAACTCTCCTTTT[CT/TC]ATTAATGACTATGGG | 221178 |
rs386768995 | multinucleotide-polymorphism | CAT/GAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037961 | CTGTCACCCAGGCTG[CAT/GAG]TGCAGTGGCACAATC | 221178 |
rs386768996 | multinucleotide-polymorphism | CA/GG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038072 | GCCTGCCACCATGCC[CA/GG]GCTAATTTTTTGTAT | 221178 |
rs386768997 | multinucleotide-polymorphism | AG/GC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24040455 | GAAATTCACAGCACC[AG/GC]CCTTGACAGGAAACC | 221178 |
rs386768998 | in-del | CGG/TGGTGTCCTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042124 | TTTGCTGAGAAAGCG[CGG/TGGTGTCCTC]TGTCCTCTGTGTCAC | 221178 |
rs386769000 | multinucleotide-polymorphism | CAC/TAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042568 | ACACAAGCGCACATC[CAC/TAT]GCCCGTGCGCGAACT | 221178 |
rs386769002 | multinucleotide-polymorphism | CAA/TAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24047115 | GCACTGAGTCCACCT[CAA/TAT]GGCGGGGTCCACAGG | 221178 |
rs386769003 | in-del | AGGGTTTGGCTTCTTACACCA/CAAACCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052060 | CCTGTGTTTGGACGC[AGGGTTTGGCTTCTTACACCA/CAAACCT]GCATCCTGTGCTGTG | 221178 |
rs386769004 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052098 | ATCCTGTGCTGTGTC[CA/TG]GGCTCCTCGGGTCTC | 221178 |
rs386769005 | in-del | CTCTCTC/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057023 | TCTCTCTCTCTCTCT[CTCTCTC/T]TCTTTCTTTCATAGC | 221178 |
rs386769006 | in-del | CTC/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057027 | TCTCTCTCTCTCTCT[CTC/T]TCTTTCTTTCATAGC | 221178 |
rs386769007 | in-del | GAGAC/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065615 | CTCACAAGACAGAGA[GAGAC/T]GTCCCCTAAGCCACA | 221178 |
rs386769009 | multinucleotide-polymorphism | ATA/TTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092945 | ATCTTCTCATTAACG[ATA/TTG]CAGATGACTATTTTC | 221178 |
rs386769010 | multinucleotide-polymorphism | CT/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100536 | TCCTTCATCTTGTAG[CT/TG]ATGGAATGTTCTGAC | 221178 |
rs386769011 | in-del | AC/CAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101497 | TGTGGTGAAAAAAAA[AC/CAA]CACATAAAACTTACC | 221178 |
rs386769012 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103247 | AAACCAGGTTATTAC[CA/TG]GTTTATTTTCTTTAC | 221178 |
rs386769013 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105282 | TGCACACCATCATGC[CA/TG]GGCTAATTTTTATTT | 221178 |
rs386769015 | multinucleotide-polymorphism | CCG/TCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24111409 | CCTCTCTGTCCTGCC[CCG/TCC]CCACCCCCACCCCAG | 221178 |
rs386769016 | in-del | GTATAT/TTTTGCACATACTTTTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24122642 | CTTTTTGCACATACT[GTATAT/TTTTGCACATACTTTTG]CACTTCAAGATACTT | 221178 |
rs386769017 | multinucleotide-polymorphism | ATG/GTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133327 | GATTGTGTAAGCCCA[ATG/GTT]GGAAATAGTGGCTCC | 221178 |
rs386769018 | multinucleotide-polymorphism | GA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134779 | TTTATGGCCTCAGGA[GA/TG]GCTTCACTCGTTGTT | 221178 |
rs386769019 | multinucleotide-polymorphism | AA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136504 | AAGAAAGAAAGAAAG[AA/TG]AGAGAGAGGGAGAGA | 221178 |
rs386769020 | multinucleotide-polymorphism | CCA/TCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24163284 | GCACTCACCTGTAGT[CCA/TCC]AGGTGCTCAGGAGGC | 221178 |
rs386769021 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174218 | GAAAGCGGTCCATTT[CA/TG]TTGAAGTTGTCAAGT | 221178 |
rs386769022 | multinucleotide-polymorphism | ATA/GTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174497 | AGCACTGCTTTCGCT[ATA/GTG]TTCCACACATTTTTA | 221178 |
rs386769023 | in-del | GT/TGA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192186 | GGGCACAAAAGCAGC[GT/TGA]TGTAAACTCTTGTTG | 221178 |
rs386769024 | multinucleotide-polymorphism | GC/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192880 | GGAGGCACTTCCAGA[GC/TT]CCAGCAGGTGGTCCT | 221178 |
rs386769025 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192914 | GAGCACTGGTAGAGA[CA/TG]GACAGGAGGAAAAGG | 221178 |
rs386769026 | multinucleotide-polymorphism | ATG/GTC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196734 | ACAGAGTGAGACCCT[ATG/GTC]TCAAAACAAAACAAA | 221178 |
rs386769027 | multinucleotide-polymorphism | CCA/TCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24200509 | ACCTCGTTCTCAGCC[CCA/TCC]AGTCTCCCACCCAAG | 221178 |
rs386769028 | in-del | AAG/GA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208702 | GAGCCCATAGGCCAA[AAG/GA]AAATCCCTGACAGTT | 221178 |
rs386769029 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211566 | ATTTAGTAAATATTG[CA/TG]TATTTATTTAGTAAG | 221178 |
rs386769030 | multinucleotide-polymorphism | CGA/TGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211733 | ATCCGGTGGCACTGA[CGA/TGG]TGATGGCCTCTGCTG | 221178 |
rs386769032 | in-del | GA/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221483 | GGAAAGGTTAAGGGG[GA/T]GCAGGATTTTCATTT | 221178 |
rs386769033 | multinucleotide-polymorphism | AA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230664 | AGCTGAGGTGATGTG[AA/TG]GACTTAACATGGGGC | 221178 |
rs386769034 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242137 | AATATGAATTTACTC[CA/TG]TGAAACAAAATCGAC | 221178 |
rs386769036 | in-del | -/AGG | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254199 | TGATTCACTGTGGCC[-/AGG]ACTGTGAACTCTGGA | 221178 |
rs386769037 | multinucleotide-polymorphism | ACT/CCA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275966 | AATGTTTTTTCCACA[ACT/CCA]ATTTTTTCAACAAAA | 221178 |
rs386769038 | in-del | GGT/TTGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282163 | GAGGCTAAGCATGAT[GGT/TTGG]GGGGGGTGGGAGTCT | 221178 |
rs397692621 | in-del | -/AG | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182510 | GAGAGAGAGAGAGAG[-/AG]CGCAGGAAAGAGGAT | 221178 |
rs397693340 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175239 | TTTTTTGTTTTTTTT[-/T]AATTTGTTTTTGTTG | 221178 |
rs397698698 | in-del | -/TTTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24072843 | TTTTTTTTTTTTTTT[-/TTTTTTT]ACATCCCCTTAAGTG | 221178 |
rs397701598 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24179598 | GTACAGATTAAATGC[-/C]AAGTCCCTATTTATC | 221178 |
rs397709098 | in-del | -/GT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170642 | AATTGGAACACCTGT[-/GT]CTCCTGAGATGAAGA | 221178 |
rs397726020 | in-del | -/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211494 | AAAGGCTTTTTCTGT[-/TTT]ATCTGTTGAGATAGT | 221178 |
rs397726571 | in-del | -/TCATGATG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074506 | ATTGTACTCATGATG[-/TCATGATG]ACTGTCCCTTATGCA | 221178 |
rs397730803 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081719 | TAAATTTAAAAAAAA[-/A]TTAAAAATTGCACAC | 221178 |
rs397744514 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262322 | TCTTTTTTTTTTTTT[-/T]AGCTCTTTTGTGGTT | 221178 |
rs397750311 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048689 | CAAAATTAAAAAAAA[-/A]GATAAATAAATTGTA | 221178 |
rs397769304 | in-del | -/AGTAG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24086072 | TCACTGTGGGAGTAG[-/AGTAG]CAGGAGAAAGCTGGA | 221178 |
rs397777316 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201459 | GTTCACTCTTTTTTT[-/T]GAGACAGAGGCTTGC | 221178 |
rs397781505 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148376 | TTTTTATTTTTTTTT[-/T]CCTGAAATGCATACA | 221178 |
rs397785266 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999611 | CAGGGTGGATTCTTC[-/C]TGCCTGAGCTGCAGC | 221178 |
rs397796149 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983241 | CAGGGATGGTTTTTT[-/T]CTGACGCCGCGCTCC | 221178 |
rs397799191 | in-del | -/C | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159113 | ATAATAAAAAAACCC[-/C]TCAATTTAGACCGTG | 221178 |
rs397812018 | in-del | -/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202602 | ACTTTTTTTTTTTTT[-/T]GTATTTGTAGATTTG | 221178 |
rs397851322 | in-del | -/G | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303212 | GGATGCCGTCAAGAC[-/G]GGGTTGACACAATGC | 221178 |
rs397851379 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102492 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 221178 |
rs397851700 | in-del | -/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978871 | ACTAATTAAAAAAAT[-/T]TTTTTTTTTTGGTAG | 221178 |
rs397851751 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102492 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 221178 |
rs397945205 | in-del | -/CT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074146 | TGAAGATCTGAAACT[-/CT]GTCTTCATTAAACCA | 221178 |
rs397951504 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154135 | ATTTTGAAAAAAAAA[-/A]GCTTGGCCGTAGCTA | 221178 |
rs397953366 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24096450 | AAATACAAAAAAAAA[-/A]TAGCTGGGCGTGGTG | 221178 |
rs397953655 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248897 | CTTTTTTTTTTTTTT[-/T]GAGAAAGAGCCGTGC | 221178 |
rs397957419 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013722 | TTTTTTTTTTTTTTT[-/T]GCCCCAGAAGACCAG | 221178 |
rs397959527 | in-del | -/GTCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024459 | TCTCTTGGGTTGTCT[-/GTCT]AGTGACAAGACCAAC | 221178 |
rs397969535 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181851 | GGGTGTGGTGGCTTA[-/A]CACCTATAATCCCAG | 221178 |
rs398021939 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015750 | GCAGGCCCCCCCCCA[-/A]TTCCTAGGTCCACCG | 221178 |
rs398021940 | in-del | -/AC | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043494 | TACACACACACACAC[-/AC]CCATGAACACACACC | 221178 |
rs398021945 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254829 | CTTCTTTTTTTTTTT[-/T]CCTTTTTATGAACCC | 221178 |
rs398021946 | in-del | -/A | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258248 | TCAAAAAAAAAAAAA[-/A]TAAAAAGAACTCTGG | 221178 |
rs398056191 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204379 | AACTGGTAAATTGTT[-/TT]AAAAGCATTGTTTTT | 221178 |
rs398070242 | in-del | -/GAT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996620 | CTGTGCTTGGCTGAT[-/GAT]TGGCTGAGATTTGGC | 221178 |
rs398070243 | in-del | -/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24247498 | TTTTTTTTTTTTTTG[-/TT]AGACAGAGTCTCCTT | 221178 |
rs398077112 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23981280 | CCATAGGAAAAAAAA[-/A]ATGTCAAGGGGTTCG | 221178 |
rs398077113 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100746 | AGACACTAGCAGATT[-/T]TGCTCTTACCTGAGC | 221178 |
rs398077114 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146644 | GAAATGCACAGCAAT[-/T]TAAAAAAAATGCCAA | 221178 |
rs398077115 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24201458 | AGTTCACTCTTTTTT[-/T]TGAGACAGAGGCTTG | 221178 |
rs398077116 | in-del | -/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304469 | CTGCAGTTTTTTTTT[-/T]TCTAACAGGCCCATG | 221178 |
rs398098691 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135228 | ATTCGAAAAAAAAAA[-/A]TACTTTTTCTTCTCT | 221178 |
rs398117104 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24222480 | TAATTATTTTTTTTT[-/T]CCATTTCAAATAAGA | 221178 |
rs527252944 | snp | C/G | 2.50216e-05 | 0.00353697 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290932 | GCACTGCTGCCATTA[C/G]CCGTAGGCAGCTCTT | 221178 |
rs527254758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285107 | AGTCAGCGTCTTTAC[C/T]GAGATGGCCAGTGAT | 221178 |
rs527288882 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24097074 | TGGCCCCGGCTGAAA[C/T]GGTGCCAGTGGAGTT | 221178 |
rs527293001 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085245 | CTCCTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAC | 221178 |
rs527302064 | snp | A/G | 0.000343741 | 0.0131054 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249480 | CGCATTTGAAAGGTC[A/G]TCCCTGATGGCCCCT | 221178 |
rs527322182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124992 | TCATAGGGTCAGAGC[A/G]GGTGGTGGCAGACAG | 221178 |
rs527331171 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044870 | AGACAGTAAATAGAA[C/T]GGTGGTTTCCAGAGG | 221178 |
rs527335683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119924 | GTTTAAACAGAATTC[C/T]CATTAGCTTTTCCAT | 221178 |
rs527345573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210387 | ATATGTTTTGTTCTA[C/T]GGTTTTTATGGTTCC | 221178 |
rs527346379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085698 | TACCTCCCGTGCTGG[A/G]CAGTGAAGAGGGAAC | 221178 |
rs527347109 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119005 | CCACCTCCTGGGTTC[A/C]AGTGATTCTCCTTCC | 221178 |
rs527357770 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24055422 | ATTTCTGTCTGCCTA[C/G]GGAGATGGAGGATGG | 221178 |
rs527363660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175746 | CATCTGTTCCAGACA[C/T]AGTGCTAGTCCCTGA | 221178 |
rs527372404 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24214939 | TCATTTCAGTCCCCA[C/G]TGAGCATCTGACATA | 221178 |
rs527373553 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24205783 | GAAATAAGATCACAC[A/T]CCTACAACTATCTGA | 221178 |
rs527374552 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295516 | ACTCGGGAGGCTGAG[G/T]TGAAAGGATCACTTG | 221178 |
rs527387332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114382 | GCATGTGTGCACATG[C/T]GCGTGTGTGTGCATG | 221178 |
rs527394769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216603 | CTTACACAGAGAGAC[C/G]CTGAAGGTACCAGAT | 221178 |
rs527413086 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073243 | TTCACCTTGCAATTT[A/T]AAAAAAATTTCTAGG | 221178 |
rs527425567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182753 | TTTCCTTTAATTTTT[A/T]AAAACTGTCATTTCT | 221178 |
rs527426926 | snp | A/T | 0.349452 | 0.229367 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254199 | TGATTCACTGTGGCC[A/T]GGACTGTGAACTCTG | 221178 |
rs527429808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004293 | TCAGGAGTGAAATCC[C/T]GGTTCTTGTACCAAC | 221178 |
rs527434857 | in-del | -/AAATA | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244862 | TGTCGCAAAATAAAT[-/AAATA]AAATAAAATATATGC | 221178 |
rs527441070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998768 | GGCCTGAGATATGGA[A/T]TCAGGTTCATTTTTC | 221178 |
rs527449498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114753 | CCACAACTTCCACCT[C/T]CCGGGTTCAAGTGAT | 221178 |
rs527453672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034478 | GTCTTAATAGAGAAA[A/G]TGATCAATTCAAGCA | 221178 |
rs527454309 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065829 | ACTAAGTTTTTAAAA[A/G]TATTTCTAAGTTCTA | 221178 |
rs527461409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301733 | GGGCCCACCCTCTTC[A/G]TGCCATGCTGACTTA | 221178 |
rs527464538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259874 | CAGACTGGTCTCAAA[C/T]TCCTGGCCTCCCACC | 221178 |
rs527464616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999481 | AATCTTCCAACCCAT[C/T]ATACAGTCTATCTCT | 221178 |
rs527467785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267794 | CCACCCATTCATTCC[A/G]TGGTCTTCACTAGTT | 221178 |
rs527479818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992480 | GGTGCTGGTGGTGGT[A/G]GATGGCTCTGCTCCA | 221178 |
rs527488302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181891 | AGGCCAAGACGGGTG[A/G]ATCACCTGAGGTCAG | 221178 |
rs527488883 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034935 | CAGGCTGTCGGAAGA[A/T]AAACTCCACCTCTCA | 221178 |
rs527494584 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254846 | CTTTTTATGAACCCA[A/C/T]TGAGCAAGTATCAAG | 221178 |
rs527514082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222524 | TTGAATGATACCTAG[A/G]TATTTTCATTCCAGC | 221178 |
rs527516079 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048502 | TTACATTCATAATTT[C/T]GTGTAATAATACATA | 221178 |
rs527537680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068482 | AATTTATATTCCTTT[G/T]GGTATGTGCCCAGTA | 221178 |
rs527557528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187884 | CTAAGTGTTCAAGTG[A/G]AAGGAAGAGTCGCCC | 221178 |
rs527574334 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24183908 | TTCCTCAGACACAGC[A/G]TCACATGGTGTTTTC | 221178 |
rs527585841 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229572 | GATTTTTCCATCCTA[C/G]ATTGACATGGCTTTT | 221178 |
rs527588108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103431 | TTGAGGTTACACTGA[C/G]CTGTGATTACACCAC | 221178 |
rs527598258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063169 | CCCAGGTCTGCCCCA[C/T]GTGAGGGTGAGCTCC | 221178 |
rs527601099 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010930 | GCTAAATGCTTTGCC[C/T]CACTGGTGACTGAGG | 221178 |
rs527607912 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24296540 | CTTTTGTTTCTATGA[C/T]CCTGAACAAGTTGCA | 221178 |
rs527629121 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165900 | AAATGTGCCCTGAGT[C/G]CTAAACAACTTGCAC | 221178 |
rs527640706 | in-del | -/TTTAT | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174566 | GATTAAAAATTTCCC[-/TTTAT]TTTATTTTTTATTAT | 221178 |
rs527641153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157162 | GCAGATTTCTCCCAG[C/G]CGTAGTCTGGGCGGA | 221178 |
rs527642184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228890 | CTTATTTATATCATA[C/T]TGTCCTAAAAATAAC | 221178 |
rs527650482 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042639 | GTATTCATTACCAGG[A/G]GGTAAACCTTACTGA | 221178 |
rs527676122 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193090 | AATCCAGGAAGGGAC[A/G]GGAGCCACTGAGCAT | 221178 |
rs527678685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198203 | TTTCACTGTGTTGGC[C/T]AGGCTGGTCTTGAAC | 221178 |
rs527680108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063653 | CCACTCAAGTGGGGG[C/T]GGCTCCTTCTCCCAC | 221178 |
rs527683414 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279172 | CAGTGGAGTGAGAGT[A/G]AGGGTTGTGGTTTTG | 221178 |
rs527684405 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987444 | TACTTCTAAGGTTAA[A/G]TATTATGTTCATTAC | 221178 |
rs527686559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980242 | GCTCAAGGGGTGAGC[A/G]CATAGGGGCGCCGGG | 221178 |
rs527701592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016552 | CAGCCAAGCAGGGCC[A/G]CTGGGTTCACCTTGA | 221178 |
rs527704017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156881 | CTCTTGGGTCTTGCC[A/T]TATGTGCCAGAGGCA | 221178 |
rs527705099 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24194063 | TTGCATCCATGGTTC[A/T]GTAGCCGAGTCTGTG | 221178 |
rs527706693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098665 | CGGATGTGGTGGTTT[A/G]TGACTGTAATCCCAG | 221178 |
rs527718843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058534 | CATAGGGCTACACAT[C/T]ACTTAGAATAATTGA | 221178 |
rs527721942 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284596 | TTGAAGCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 221178 |
rs527723561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981063 | AACATTTGCAAAAGA[A/C]AAATATATAAAGCCG | 221178 |
rs527739937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017103 | GGGCCCAGCCCTGGG[C/T]CAGGGCAGAGAGTTG | 221178 |
rs527741225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198088 | GCAACCTCCACCTCC[C/T]GGATTCAAGCGATTC | 221178 |
rs527789519 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059128 | AGTCGCCCACCACCA[C/T]GTCCTGCTAATTTTT | 221178 |
rs527793800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078681 | GAAGCAGTTGTCGCC[C/G]TAGTCCATAAAGTCA | 221178 |
rs527799504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052002 | TTGCCAGTCCTTTGG[A/C]TTCCTCTGCGTGCAC | 221178 |
rs527824720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017396 | CTTAGAGCTTGAAAA[C/T]GCACAGTGTGATCTA | 221178 |
rs527825997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248107 | AGGGCATGCAGGCAG[A/G]GCTTACAGGCCTCCA | 221178 |
rs527828678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156658 | ATAAAATATAGCAAA[C/T]GCACCTTATCCATTC | 221178 |
rs527828971 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169299 | TGGAGTGAGGTGCTA[A/C]CCCTGGAAAGCTCCC | 221178 |
rs527829182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011177 | GCTGCTTCAGCCCAG[C/T]GAGACCCATCTTGCC | 221178 |
rs527836263 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093157 | CCTATATTTCATAAG[G/T]TTAAAAGGTCAGGCT | 221178 |
rs527837749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046098 | GATTTTTTTTTAAGT[C/T]TTGCTGGAGTGTATC | 221178 |
rs527839977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004096 | TCCTCAAGGTCGTTC[A/G]GGGACTTGGGTTCCT | 221178 |
rs527848986 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029018 | GCTCTCTTTTGTTTC[C/T]TCGTATGTGGTTTTT | 221178 |
rs527851558 | in-del | -/AAGCAGCCCAGTATGA | 0.0441095 | 0.141807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168571 | TGTATCGCAGCACAC[-/AAGCAGCCCAGTATGA]AAGCAGCCCAGTATG | 221178 |
rs527859569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120941 | GACTGTGGGAAGCTT[C/G]CTGGGGTCTAGGTCT | 221178 |
rs527863264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011868 | CTTGGGGGACCATGA[G/T]GGATGATCCCACAGA | 221178 |
rs527865167 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004958 | TACTGTCTGTGAGAA[A/T]AAATCAAATGAATTC | 221178 |
rs527876442 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116950 | GAAGGCAGCTGTCTG[A/C]AAGCTGGGAAGAGAG | 221178 |
rs527886628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247659 | GGCTAATTTTTTTGT[A/G]TTTTAGTAGAGACAG | 221178 |
rs527898351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174494 | CACAGCACTGCTTTC[A/G]CTATATTCCACACAT | 221178 |
rs527911288 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24010916 | CATGTCAAATGGTTG[C/T]TAAATGCTTTGCCCC | 221178 |
rs527925381 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046620 | TGTGGGTAGCAAGAG[C/T]TTGTTATTAGTTCCT | 221178 |
rs527927071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294504 | ATTTCTGGGAAATGA[A/G]TGAAAACATTTTTAT | 221178 |
rs527928551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121379 | CTTGCCTCACACCCC[A/G]TTACATCTTTTTATA | 221178 |
rs527932324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208687 | ATTAAGACTTTTAGG[A/G]AGCCCATAGGCCAAA | 221178 |
rs527933780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259063 | GTGAGCATCTCGTCT[C/T]ATGCCTGGCCTTGTG | 221178 |
rs527943059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253008 | CTTGAAGAAGTGTAT[A/G]CTTATTTGGGGAGGA | 221178 |
rs527955175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005473 | AGTACGAGAAATGGA[A/G]TGTATGCAGGGAGAA | 221178 |
rs527956085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300221 | ACATGGCCACCTTGG[C/T]GATAATCCTTGTGAC | 221178 |
rs527956951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000391 | GGCGTGGGGAGCCCA[A/G]TGAAAGACAGTGCTG | 221178 |
rs527957260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081419 | ATGTCCTTGGATATG[C/T]ATGCATCTGTGAAAT | 221178 |
rs527962915 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174209 | GTTTTTAAAGAAAGC[A/G]GTCCATTTTGTTGAA | 221178 |
rs527971948 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186178 | AACCATCACAACTAC[C/T]AGTGAGGAAACGGGA | 221178 |
rs527979387 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136841 | TTTATTTATTTATTT[A/T]TTTTTTGAGACGGAG | 221178 |
rs527983620 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24256453 | CTGTACCCCATAAAT[A/G]TTGTACAATTATTAT | 221178 |
rs527994732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000728 | GGTGTGAATTTGGGA[A/G]AGCTCTGGGTCAGAG | 221178 |
rs527995034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115730 | TGTGTGCTTCCGGTT[C/G]CAGATTTCTCAGTGG | 221178 |
rs527996191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214378 | TGACCTATAACTATC[A/T]ACTTTACATGTTACC | 221178 |
rs528019060 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24203285 | TAGAGGATGTAAATT[A/C]GTGTCAGGGTAATCA | 221178 |
rs528026333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180359 | TTGATCTATATGTCT[A/G]TCCTTGTGCTAGTAC | 221178 |
rs528029424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225456 | CCAAAGAGGGTGTTA[C/T]GGCCTGTCACAGCCT | 221178 |
rs528040453 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154534 | TTGCTAACGGGGGGG[A/G]GGGGCACATAAGGGA | 221178 |
rs528042938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100705 | TTCTACTCACCAGTT[A/C]TGTTTCTCTTCAAAA | 221178 |
rs528043434 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169611 | GAGGTCATGTGGCTC[C/T]GGGAGCATCAAGATG | 221178 |
rs528043989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032282 | CATGCTGTATTCAAC[A/G]CTGAGCCTGCTCTCT | 221178 |
rs528044184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232626 | AGCTTACTGCAGCCT[C/T]AACCTCCCAAGGTCA | 221178 |
rs528045803 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24195215 | TACAATATGTGGCCT[G/T]TTGTGACTGGCTTCT | 221178 |
rs528053443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066035 | AGCATTTGCCTAATA[A/T]TGCCAAGTACATAGT | 221178 |
rs528069673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139806 | GGCGCGGTGGCTCAC[A/G]TCTGTAATCCCAGCA | 221178 |
rs528079271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026165 | AAAGTATGATTTTTC[A/G]TGTCGTTTTATGGTA | 221178 |
rs528086506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060277 | GCCCAGAAATACTTA[C/T]AACCTGCACACTTAC | 221178 |
rs528088310 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304890 | CAGACATTCCAACTT[C/T]AGATGTGTTTATAGA | 221178 |
rs528088628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990019 | TTATAAGCCACCCAG[A/G]TTATGGTATTTTGTT | 221178 |
rs528091547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232121 | GATCTGCCATCTGCA[C/G]CCTGGAGAACCAGGA | 221178 |
rs528103039 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147500 | TGGAAGTGGTGATTG[C/G]TCGGTGCTCTCAATC | 221178 |
rs528104186 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004315 | TGTACCAACACCTAT[C/G]TGCGCACTTTGAACA | 221178 |
rs528106509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276782 | GTCATCATTATTAAC[G/T]TTCATCTGTAGTTGA | 221178 |
rs528125579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281901 | CCGTGCATCACCAGT[A/G]CATGAGCTTGAACTC | 221178 |
rs528130838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134347 | CCAGTGAGTAGTTAT[C/T]CTCTGGAAGATTCTG | 221178 |
rs528132590 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158179 | TTGAATATTCAGGCT[-/C]CAGTTAGAGTCTTGA | 221178 |
rs528178111 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023334 | TCTGTGAAAGCTGTA[G/T]ACATTAAGGCATAGC | 221178 |
rs528179032 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159552 | TACATTCGAGTGGCA[C/T]ATGTGTTATGATTGA | 221178 |
rs528191295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134729 | ACCAACATTGCTCCC[A/T]GAGCCTAGAAAACAT | 221178 |
rs528195314 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24131081 | CAGTAAGGAAATTCA[A/G]GAGATTTTCATATAA | 221178 |
rs528195635 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054653 | AAAGAGTACAGAAGA[G/T]AAAATATGTGAAATA | 221178 |
rs528202735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128304 | CATTGTGGCTTCATC[A/C]CCAGAAATGCTCTGC | 221178 |
rs528202749 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992663 | GAAATGAACACAAAG[C/T]GGTCCATGTGCTACA | 221178 |
rs528214893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245912 | GGTTTTGTGTGCTCT[A/G]CTGTGCTGACTCTGA | 221178 |
rs528217944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200429 | TAAGGACAAAGACAA[A/G]TAAACACCATGTATG | 221178 |
rs528224795 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158958 | ACATAGTTTCAAATA[C/T]AGTGCTTTCTTCACT | 221178 |
rs528229813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089031 | ATGGGACACGTTCAC[A/T]GGTGGCTTTGAAAAG | 221178 |
rs528231379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055260 | TCCCCAGTCCTCTCC[G/T]TCTCCTTCAGTGTTA | 221178 |
rs528235136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096015 | TCTGAGAGGCTGCCT[G/T]GGTCACTTCCCAGCT | 221178 |
rs528242554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166503 | CCAGCTTGGTGACTT[C/G]AGGGACCCTTGAACA | 221178 |
rs528254164 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148105 | TCAGTTCTTTTCCGC[A/G]TACACCCAGGGGTAA | 221178 |
rs528255708 | snp | A/G | 3.30584e-05 | 0.00406548 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286828 | AGTGAGGAGCAGGAC[A/G]AGGAGGCCAGCCAGA | 221178 |
rs528273243 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260334 | GGTAGCCTAAGAGAA[A/G]ATTACACTGGTCAGG | 221178 |
rs528275437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245192 | GTTGTTTGATGGGAC[A/C]TGTGTGTCTACAGTT | 221178 |
rs528290948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165935 | ACTTTTAAACACATC[C/T]GGGTTGTGTGTTGTG | 221178 |
rs528294113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083492 | GAGTTGAAGTCCAGG[C/T]GGAGCTTGCGGGGAG | 221178 |
rs528306400 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282167 | TAAGCATGATGGTGG[-/C]GGGGTGGGAGTCTGG | 221178 |
rs528311191 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24129418 | CTTGTCCAGAGAATC[A/G]TTGAGGATGTGAGAA | 221178 |
rs528320117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212020 | TCGCCATTCCCCTAC[C/T]AGTGTGTCTACCCCA | 221178 |
rs528336995 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24077073 | AAAATACGATCTCTG[A/G]TGGCTTAGAAGAAAA | 221178 |
rs528337266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042918 | CTGTTTAGATTTACA[A/G]TTGATAGAATGATGC | 221178 |
rs528351857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008065 | CAGCCCCACTCATGG[C/G]AGCCGAACCACCCAG | 221178 |
rs528356259 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113666 | CACGAGGTCAGGAGA[A/T]CCAGACCATCCTGGC | 221178 |
rs528366574 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24005410 | CTCAGGAATATAGTG[C/G]TCACCTGGTGCCTAG | 221178 |
rs528372401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171505 | CAGATGACAGTGGGA[A/G]TGCCACAAGGATGGG | 221178 |
rs528384094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061114 | GTGGCTAACAGGCAC[A/G]TGAAAGAAAGCTCAA | 221178 |
rs528398039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078168 | GCAGTGCCAGCCTAG[C/T]TCACCTGCAAATACC | 221178 |
rs528400885 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095419 | GGCTGGGGTAGGGGG[G/T]GCAGAATAGGGGAGT | 221178 |
rs528405613 | in-del | -/TATATAA | 0.0573587 | 0.15934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189902 | TATATATTATATAAT[-/TATATAA]TATATTACATAATAT | 221178 |
rs528408419 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150362 | TCAGTGGCATGGCAG[G/T]GCATCTCAGCACTGG | 221178 |
rs528432742 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24083404 | AAGTCACAAACAAGT[C/T]AGCAGAGTCAAGGAG | 221178 |
rs528441688 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136187 | AAATTCCTTATTTTT[-/A]AATAAACAATCATGT | 221178 |
rs528443258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296787 | CACAGAGGCACTGTC[A/G]CATTTTTCTAGTAAG | 221178 |
rs528445560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038225 | GCCAACTAGGCTAGA[G/T]TTTTAACAAATATAT | 221178 |
rs528454608 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980883 | AAGCTTGAGCCACTG[C/T]GCCTGGCCAACAAAG | 221178 |
rs528456164 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110619 | TCATCAAACCTTGAG[-/C]AAACACTTGCCATGG | 221178 |
rs528477794 | snp | C/T | | | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253177 | AGAAGGGTGGGGTGT[C/T]TGTCTCCAGGGACCC | 221178 |
rs528492219 | in-del | -/A | 0.132751 | 0.2208 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293230 | AGAAAAGTTCAGTGG[-/A]AAAAAAAAAAACAGG | 221178 |
rs528494888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038911 | GCTAAAAGGGAGCAC[A/G]CAAATCCAGAGAAAC | 221178 |
rs528499759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177040 | AAAGTGCTGGGATTA[C/T]AGGCACGAGCTGCCG | 221178 |
rs528500393 | snp | C/T | | | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033594 | CTTCAAGGGGGCTCA[C/T]GAAGGTTGTGGATCC | 221178 |
rs528500472 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224421 | GCCCTGTCCGCGAAT[C/T]CAGAGGAAAGTGAAG | 221178 |
rs528504622 | in-del | -/CTAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126902 | CTAGGAATCTTTACC[-/CTAA]CTAAACGTTTTCTCT | 221178 |
rs528540289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990988 | TTTTATTTGCCTGGT[A/G]TACCCCTGGCCTTGT | 221178 |
rs528540932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066862 | AGAGACTCCGGCCAG[A/C]TCTGGCAGACTGGTA | 221178 |
rs528555409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997699 | ACAGTGGAAGGTGAA[A/G]GGGGAGCAGGCGTGT | 221178 |
rs528560969 | snp | A/G | 0.000319846 | 0.012642 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223942 | GGAGGGAGAGTCCTA[A/G]GAGTGGGGCCCCATC | 221178 |
rs528562713 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276079 | GGAAAACAGTATGGA[A/G]AGTCCTCCAAAAATT | 221178 |
rs528566038 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230502 | GACTTCCAGGCTGGC[A/G]GGAAGAGTGTAGAAC | 221178 |
rs528577119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107818 | ATAAGATGTGTACTG[C/T]TCTATCGGCACGTTA | 221178 |
rs528579497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302273 | CTTCTTTTTGGTTAA[C/T]GTGAATTAAGAATTA | 221178 |
rs528587987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000732 | TGAATTTGGGAGAGC[C/T]CTGGGTCAGAGGCAT | 221178 |
rs528590334 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026864 | GCCTCCGCCTCCCAA[A/C]GTGTTGGGATTACAG | 221178 |
rs528592043 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24302315 | AAAAATATAAAAATT[A/G]GCTGGGCGTGGTGGC | 221178 |
rs528592324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033768 | CCTCCGTCATGTGAC[A/G]GGTGAGCCCTGCCAT | 221178 |
rs528603403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140569 | CCCTACAGAGTCAAA[C/T]GTTCCTCTTCAAAGC | 221178 |
rs528604751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268849 | TTTTCACTTGTAGTG[C/T]GGGTTACTAAGGCTA | 221178 |
rs528607307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189242 | TTTGGGAGGCCGAGG[C/T]CGGTGGATCACGACG | 221178 |
rs528622684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009162 | CTGCTCTGGTTCTTC[C/T]TGGAGCTGACACATT | 221178 |
rs528628053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027512 | AACTTTTTACTTCCT[A/G]ATTTCTGTGTTGTAT | 221178 |
rs528639330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102568 | CAACCTCCTTCTCCC[A/G]GGATTAGGTGATTCT | 221178 |
rs528652925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194576 | CAGTTTGAGGATTTG[C/G]TAGTCAGTGATCCTG | 221178 |
rs528661210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985501 | TCTGTCCCATTTTTC[A/G]GCTCAGGGTCTTCCT | 221178 |
rs528674753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140961 | GGGCAAATCACCTGA[A/G]GTCAGGAGTTCGAGA | 221178 |
rs528676182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079354 | ACAGAGCTGAGGGGG[G/T]GACATGATCCACGCT | 221178 |
rs528677953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275358 | ATGGTTATTGAACAA[A/G]AGCATTATAAATTCA | 221178 |
rs528684491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096846 | CATGCAGGCCAGATC[A/T]TTTCAGGCTGTGGAG | 221178 |
rs528698411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021289 | TTGGAGAATCCTGAA[A/G]ATGCCTGTTTGCTCA | 221178 |
rs528698530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237123 | AGCACTTTCTGAGGC[C/T]GAGGTGGGTGAATCA | 221178 |
rs528707859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102861 | TGTTATACCCAAGAA[A/C]TCTTTGCCAAAACCA | 221178 |
rs528715017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280488 | TTATTTTACTGAGAT[A/G]CACTTTTTTTTTTTT | 221178 |
rs528721725 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081006 | TCATCCTCTGGTAAG[A/G]AAAGGAGGAAAATAC | 221178 |
rs528735457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015406 | GGACTGTACATTTTA[A/T]GAAAATCCTTTCTTC | 221178 |
rs528746858 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135804 | TGAGGGGAACTGTAA[A/G]GAAATGCCAGTGTAT | 221178 |
rs528751203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129550 | AATTAGTAGGGACAG[G/T]TTTGTTATTTGGCTG | 221178 |
rs528756696 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062497 | GCCCTGCCGCTCCAG[A/G]GCTCTGTGAACCTGG | 221178 |
rs528764957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236462 | TAGCTGGGCGTGGTG[A/G]CACGCACCTGTAGTC | 221178 |
rs528768930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164977 | GGAGCTGTGGCAACA[C/T]CGCAGAATGCAAGGA | 221178 |
rs528781771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157704 | AGAAAGGAGTTTCCT[C/T]TCTGCCCTGTACCTC | 221178 |
rs528782710 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979599 | AACAATAGCACAGCC[C/G]CGGCCCTGGAAGCCG | 221178 |
rs528782740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285510 | CTGCCTGCCTGCCTG[C/T]CTTCCTCCCTCCCTC | 221178 |
rs528794765 | in-del | -/TCCCTCCC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278971 | CCTTCCTTCCCTCCT[-/TCCCTCCC]TCCCTCCCTCCCTCC | 221178 |
rs528803006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009220 | TGTGGAAGTGAGAGG[C/T]TCAGCTGGTCCAGCA | 221178 |
rs528805668 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280090 | AATCAGAGCTCATTG[C/G]AGACTGGAAATCCTA | 221178 |
rs528807131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090954 | TGCTGTTTGCCTGTT[C/T]AGTGACTTCTGGTCT | 221178 |
rs528823516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215031 | TCCTGAATTCTGTGT[A/G]TTGGTTATGTTCGAG | 221178 |
rs528838313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095540 | CCTGATGCCACGGAG[C/G]TATACGTTTAGAAAT | 221178 |
rs528838342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294543 | ATTCTGAATTGCACT[A/G]GGTCAGCTCCCTTAA | 221178 |
rs528838678 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24005921 | TAGAGCTGATCTTCT[A/G]AAAGACCGTACTGTT | 221178 |
rs528838920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243590 | ATTTATTTTAGCCCT[C/G]GTGTCTTAATCAGTA | 221178 |
rs528863941 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133477 | AAGGACAGACAGGGT[C/T]GGCCCTGGAACTAGA | 221178 |
rs528875382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061177 | CCACAGTGAGATACT[A/G]TCTCACACCAGTCAG | 221178 |
rs528883228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259250 | CTTGTGAACAGATCA[A/G]TGCATCTTTCTGCTG | 221178 |
rs528884176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214419 | TCACGCCATGAGAAT[A/C]ATTAATATTTTGATG | 221178 |
rs528887903 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151692 | CATCACCAACCTACC[A/G]GAGAGGGCTCAGCTT | 221178 |
rs528901024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096133 | AGTGACTTTTCATTG[C/G]GATCCTACCACCTGC | 221178 |
rs528901319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300324 | AACCTCAATGCTGAT[A/G]TGGGCTGTGATACAA | 221178 |
rs528902950 | in-del | -/CTGCGACCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24007531 | TGCGAACTTGGCCCA[-/CTGCGACCT]CTGCGACCTCTGCTT | 221178 |
rs528909006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221774 | AGAGGAAAAAGATGC[C/T]GAATTTGTTTAATTT | 221178 |
rs528912829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055419 | TTAATTTCTGTCTGC[C/T]TAGGGAGATGGAGGA | 221178 |
rs528939942 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306227 | TGGTTCACAATATAA[A/G]TATTTTGTAAAAGCC | 221178 |
rs528946640 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180454 | ATTTGTTTTCTTTTC[A/T]AGATTGTTTAGGCTA | 221178 |
rs528970038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258540 | CAAGAGTTGTCGTGC[A/G]TTCCTGTAGTACCAG | 221178 |
rs528973187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228725 | TTTTTTTATTCAGCT[C/T]ATTAACAGTAAGGTT | 221178 |
rs528974680 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086437 | AAGACACCAGGGAGA[-/G]GGGCTGCTCATAGGG | 221178 |
rs528993600 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026153 | TATATTCCCCTCAAA[A/G]TATGATTTTTCATGT | 221178 |
rs528995357 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220409 | GACCATTACTACTAA[C/T]GTCAGTGCCTGTGAA | 221178 |
rs529001527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056367 | CATCTGGTTAACCAC[A/G]TAGATCTGCATTTCG | 221178 |
rs529008569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043454 | AGAACATTGCACCTC[C/T]CAGGTTCTGGACCTT | 221178 |
rs529009612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186767 | TTGAAATGGGCAACA[A/G]CGCTATTGAGGCGGT | 221178 |
rs529025892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015208 | CTGGATTTTTATAGT[A/G]AACAATGACCTCTGT | 221178 |
rs529026880 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305529 | TCAAGTATTCTCATC[C/T]TCCATTTGCCAAACT | 221178 |
rs529042907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049953 | TCTCAGCTCACTGCA[C/T]CCTCTGCCTCCCCGG | 221178 |
rs529048220 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084094 | CAGAAAGAGAAAGGG[A/G]GAGAAAGAGAGAGCC | 221178 |
rs529066671 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24238445 | TACAGGCGTGAGCCA[C/T]TGCCCCCGGCCTCTC | 221178 |
rs529076358 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24070542 | CCTTACTTTGGGACT[A/G]TGTGTTTATTGTGAT | 221178 |
rs529084624 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272878 | AGCGCAGTGCCTGGC[A/G]CACATTAAGATGCCA | 221178 |
rs529097243 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054330 | TTAGATAGATGAATG[C/T]GAAGTTTAACGAAAT | 221178 |
rs529102284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191850 | CTCCTGCATACCTCA[C/T]CAGAGTAATGAAAAT | 221178 |
rs529102663 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156255 | ATTTTTGAGGAATTG[A/C]CATACCTGTTGTCCA | 221178 |
rs529107415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084350 | GCTGAGCCCGCGCAT[A/G]ATGGAGATGCTACTT | 221178 |
rs529117338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234162 | ATTTGTAATCAACTT[A/G]TCATGATGTACTGCA | 221178 |
rs529117991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277963 | GAACACAGGAGTCAT[C/T]AACTTTAAGGGACTT | 221178 |
rs529119011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119025 | ATTCTCCTTCCTCAG[C/T]CTCCTGAGTAGTTGG | 221178 |
rs529139023 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24052619 | CTGTGGATACTGGCC[G/T]GGTGACAAGAGAACA | 221178 |
rs529146376 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24080496 | CACATAAATACAGAA[C/T]TGGTGGGAAGGGAGG | 221178 |
rs529159318 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989895 | AGGATGCAGTGAGAT[A/G]GTACCATCTGTGAGC | 221178 |
rs529160716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038973 | AGCCCTGTGACACAG[A/G]CAGGGAAATAGGGGC | 221178 |
rs529160823 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212469 | GTAACCACCCCAGGG[A/G]CAACTGAGGCATTGG | 221178 |
rs529165053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162026 | TCCTAATGTCCCCCT[C/T]CCCCGTCTTGCAAAC | 221178 |
rs529179070 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184996 | AGTGCGGGTGCCTTT[C/G]AAAGTGGGCACTGGG | 221178 |
rs529183871 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301434 | TTTAAGGCAGAAAAA[C/T]CCATGTTATTAATTT | 221178 |
rs529192537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155672 | AAATGGGACATTTTT[A/T]AAAACTGTGGTAAAA | 221178 |
rs529194013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119745 | CACTGTAAACAATTC[A/G]GGATTCCTGCAGTAG | 221178 |
rs529195046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277390 | CGGAGCTTGCAGTGA[C/G]CCGAGATCGCGCCAT | 221178 |
rs529197431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202351 | AACAGCCACACCGAG[C/T]AGATGGCCCAGCAGC | 221178 |
rs529215130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247553 | GGTGCAATTTCAGCC[C/T]ACTGCAACTTCCACC | 221178 |
rs529221984 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037963 | GTCACCCAGGCTGCA[G/T]TGCAGTGGCACAATC | 221178 |
rs529222854 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098935 | ATCTCAAAAAAAAAA[-/G]AAAAAAAGAAAAAAG | 221178 |
rs529223589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039534 | CTTATTTAGGTTTCT[C/T]TTATTATCAAGTTCA | 221178 |
rs529240967 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161319 | GTGGCAGAGTCTGGG[A/G]AGCCTGGCGCGGCGG | 221178 |
rs529242676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246715 | AATGTATATCTAAAT[G/T]AGCTGGGCGTGGTGG | 221178 |
rs529246450 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145998 | CTGCAGCTGAATGTG[G/T]TGAGGAGTGGCAGAC | 221178 |
rs529259214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991788 | GAGACTCTGAGTTGG[A/G]GGCAGGTGGGCTGGG | 221178 |
rs529261801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167863 | ATTCATTGTTTTATT[C/T]ATTCAGCAAATGTTG | 221178 |
rs529273453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107876 | TTATGGAAGATGCTC[A/G]CTCGCACTATTCTGG | 221178 |
rs529285525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073076 | TGATAATGTCCAGTT[C/T]TTTTAATCCAAGGCA | 221178 |
rs529286783 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24273736 | TAACATGTTTATAGA[A/G]CATCAAAGGCAGATA | 221178 |
rs529291445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287947 | ATTCAGTGCTGAAGA[C/T]AGGTTGAAGTCAGAG | 221178 |
rs529296938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985679 | GGAAGAGAAGGCTGT[C/T]TTTCTTCATTATTGA | 221178 |
rs529297927 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034281 | CTGATAATCTCCTTC[A/G]CTCAACACAGTGCTT | 221178 |
rs529298314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998614 | TTTCTTTTAGGGATC[A/G]TGATTTTTTGCTGTA | 221178 |
rs529305698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067904 | ACATGGGGTTTCACC[A/G]TGTTGGCAAGGTTGG | 221178 |
rs529305763 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24111123 | CTATGTTGCCCAGGC[C/T]GGTCTTGAACCCCTG | 221178 |
rs529316752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027576 | TATTATTTCCTTTCT[G/T]CTACATTCTTGGGTT | 221178 |
rs529321581 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983067 | AAGAGTCAAGTGAAG[C/T]TGATCGAAAACCAGC | 221178 |
rs529323939 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173361 | ACTCATTAGTTCTTA[C/G]TTGTGTGTGTGTGTG | 221178 |
rs529330782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141004 | ACAAGGTGAAACCCT[A/G]TCTCTACTAAAAATA | 221178 |
rs529337898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208023 | AGTAATTTAGGGAAG[G/T]TGGAGCCGCACTGCC | 221178 |
rs529346040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252159 | CCCAGGCTAGAAATC[C/T]GAGATCAACACGTCA | 221178 |
rs529351499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062446 | TGGCGCCAGGGTGCA[C/T]GGTGCTGGGAGCCAA | 221178 |
rs529367951 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092789 | AGATTTCTTAGCAGT[A/C]ATATTTGGGCATCTG | 221178 |
rs529411104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179395 | TTTACATTTCCATCA[A/G]CTATGTATGGGGGCT | 221178 |
rs529413371 | snp | A/G/T | 5.14252e-05 | 0.00507054 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251901 | TTCAGAGCTGCTATG[A/G/T]GCCCATCTGACCGTT | 221178 |
rs529417817 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245800 | CACTGTGTTGCCCAC[A/G]CTGGTCTTGAATTCC | 221178 |
rs529418203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213568 | CCATGCCCGGCCAGG[A/G]TCTTTCTTATCCTAG | 221178 |
rs529421323 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24193464 | AGGAGTGAGGCCTGC[-/G]GGGGGTGCTCCCCAG | 221178 |
rs529430511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257266 | TGTCCAGTTTACTTC[A/G]CTGTTAGACTTGAGT | 221178 |
rs529435298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292865 | GCTGGGCATGGTGGC[A/G]GGCACCTGTAATCCT | 221178 |
rs529438501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062854 | TTTGGAGTGGGTTTT[G/T]CCAGGAAATTACTTT | 221178 |
rs529444602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021770 | AGGCTGGAGTGCAGC[A/G]GCATGATCTTGGCTC | 221178 |
rs529456662 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057230 | AAGCTATCCCTCCCC[C/G]CTCCCCCCAACCCCA | 221178 |
rs529457179 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232814 | TCGGCCTCCCGGAGT[A/G]CTGAGATTACAGGCA | 221178 |
rs529475224 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136522 | GAGAGAGGGAGAGAG[A/G]AAAAGAGAGGGAGGG | 221178 |
rs529478090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015872 | ATGAAGTTGTTGGTT[C/T]TTAGAAATAATTTAA | 221178 |
rs529482892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213057 | CTGCCCTGCTTGGGT[C/T]GGCCCGTCTCCACAG | 221178 |
rs529493399 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130278 | CGGCCAGTGGGACTA[C/G]GACTAAGTGAGCAGA | 221178 |
rs529494290 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24152092 | TGTTCAGGCTGCTGT[A/G]ACAAAATACCTTAGA | 221178 |
rs529494563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050628 | GACAAGAATCCACAA[C/G]AGGCGAAGGCATTTT | 221178 |
rs529508605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097940 | GGAAGTTTCAGAATA[A/G]GCCACTGTGGTTTTG | 221178 |
rs529516444 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304665 | GAACATTCTGTGACC[A/G]CCTGATGTCCATTCT | 221178 |
rs529535239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022128 | TCTCACTGCAGCTTC[C/T]ACCTCCCAGATTCAA | 221178 |
rs529545853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220015 | GCCTCCCAGTTGTAC[C/T]GTGTGTCGTTGACTG | 221178 |
rs529564551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016418 | TCAGTTTTCTTTAAT[C/T]GACTTCTCACGTTTC | 221178 |
rs529566523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002964 | TTCTGAATGTGGGGG[A/G]TGAACAGAGAAAATT | 221178 |
rs529574168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091698 | CACCTGTAATCCCAG[A/G]TACTAAGGAGGCTGA | 221178 |
rs529584448 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113174 | TGTAAACCACTATGT[-/G]CAAACCACTATATCT | 221178 |
rs529586112 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184821 | CAGATTTTTTTTTTA[A/G]TAAAATACTTCTTTA | 221178 |
rs529591710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085874 | AATAGTGCAAAGCAC[A/C]GGAACCAGGGCGCAG | 221178 |
rs529597021 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24056924 | TTTTTTTTTTTTTTC[A/G]ATGAATGGAGATTTA | 221178 |
rs529605767 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304021 | GTCAGAAGGCACTCT[A/C]AAAGAGCCGCACTGC | 221178 |
rs529612841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158351 | AGAAAGCCACTGCGG[A/G]AGACCTAGGCTTTTA | 221178 |
rs529622753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125086 | TGTCTCTCCTCTCTG[C/T]CATTTGTTTCCTTTC | 221178 |
rs529633036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010487 | TTTCATCTTTGTAGC[A/T]ACGTTATTTAGGAAT | 221178 |
rs529634101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199072 | TTTTGTATTTTTTAC[A/C]GAGACAGGATTTTAT | 221178 |
rs529659242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165047 | GCCATGTGCTGTGGT[C/T]AGGATGTCAGCTTCG | 221178 |
rs529660464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244487 | GTAACATAGCCTATA[C/T]TGGCTTTTTACTTTT | 221178 |
rs529668026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206356 | GCAAATCAAAACCAG[A/G]ATGAGATACCATCTC | 221178 |
rs529668497 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164975 | GGGGAGCTGTGGCAA[C/T]ACCGCAGAATGCAAG | 221178 |
rs529668828 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037212 | CTGTCATAGGGTGGG[C/G]GGAGGGGGGAGGGAT | 221178 |
rs529673241 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038036 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 221178 |
rs529705064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001090 | ATTATTATGATCTGA[C/T]ACAGTTCTTCCAGGC | 221178 |
rs529710064 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064340 | AGTACAATTAAATCA[A/G]TGGGAGAGCAGTAAC | 221178 |
rs529712916 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143333 | CCCTTTCTCATTTTA[C/G]TTCTCCCATTTTTCC | 221178 |
rs529719114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988239 | GGCGTGAGCCACTGC[A/G]CCCAGCCAATTTTGT | 221178 |
rs529722432 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164510 | GGATGAGATGGGTGA[G/T]CAGGTACCATCCTGG | 221178 |
rs529724136 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030002 | GGGAATTCATAGCAA[A/T]ATTGAGTGGAAAGTA | 221178 |
rs529730314 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186445 | TCTTCAAACCAAGAG[A/G]GAACATCAGCCATAG | 221178 |
rs529769174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291162 | TTGTTGTATTGTTAT[A/G]TTGCTTACCTGTATT | 221178 |
rs529779823 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170488 | ATCTCTAAATGAAGA[A/T]GGAATTGTCTGTCGT | 221178 |
rs529783318 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115955 | CAGAGCAGGTGACTC[A/G]GGAGAGGACAAGGTG | 221178 |
rs529786002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255348 | TCCCTTGTCTTCTCT[A/G]TCATGGTGGCTCAGG | 221178 |
rs529794416 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105047 | GGAGAAGAAGTCACT[A/T]GGTCTTCTGAACTCC | 221178 |
rs529803222 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189237 | AGCACTTTGGGAGGC[C/T]GAGGCCGGTGGATCA | 221178 |
rs529807916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296032 | AGATTGTTTTTAGAC[C/G]AAGCTACATTGATTT | 221178 |
rs529811333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024184 | TGGCTAAGGGAGGTG[A/G]CCAGTCACACTGTGA | 221178 |
rs529817482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211049 | TTCAGATAGTACATT[G/T]TTAGTGTCTAGAAAT | 221178 |
rs529818058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127048 | CCGAGGTTTGTATAA[C/T]GAAGTTAGTAATATT | 221178 |
rs529826714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260909 | ACCTATGTATGCCTT[A/C]AGTTATGTTCATGGC | 221178 |
rs529830343 | in-del | -/CTCTCT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057027 | TCTCTCTCTCTCTCT[-/CTCTCT]TTCTTTCATAGCGTC | 221178 |
rs529834747 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109160 | TTCCCGCCCTCTGTC[C/G]AAGTGTTCTCATTGT | 221178 |
rs529835558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176841 | TCACCCAGGCTCACT[A/G]CAACCTCCGCCTCCT | 221178 |
rs529849110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024567 | TGCTGGTGGCCACAC[A/G]GCACGGTTCTACAGA | 221178 |
rs529851805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290482 | TAACGCTTGCGGAAA[A/C]CATGGCAGGGCAGCT | 221178 |
rs529852490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175803 | CGGATCTAGGTGTCA[C/T]TTTTCTTCTCCCACA | 221178 |
rs529853819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022335 | AGCCACTGCGCCTGG[C/T]GAAAAATCTTAATGT | 221178 |
rs529863063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094059 | GCCTGCCTTCTATAC[C/T]GGAATGTCCTGAACA | 221178 |
rs529864492 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146732 | TTTAATTAGTATATA[C/T]CTTTGTGTCTAAAGC | 221178 |
rs529874827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983311 | TGGTCATCCTTCTAT[A/G]TTGTCTGTGTCCTAA | 221178 |
rs529877942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210460 | TGGAGTAGGAGGCCA[A/G]TTTTATTATTTTGCA | 221178 |
rs529878449 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144273 | ACATGCCTCGTGTAC[A/G]TCACAAACATCACAC | 221178 |
rs529878531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060056 | GTTCCAATGACATTC[G/T]TCACTGAACTAGAAA | 221178 |
rs529879941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217363 | ACAGTTGCTGCTAGA[C/T]ATCCTACAAAGCACA | 221178 |
rs529886823 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011153 | AGAGCCACACTGCAG[A/G]AAAACAAGGCTGCTT | 221178 |
rs529899850 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183381 | GAAACATTTAACAAC[A/G]GCATCATCATGCCTT | 221178 |
rs529900846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019013 | AACAGACATATTAGA[A/G]TTTGGTTGATATTCA | 221178 |
rs529906211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133155 | TCCTGGTACCCAAAG[G/T]CCCAGTGGGATTAGA | 221178 |
rs529915957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018463 | ATCTTTTTAAATTCC[G/T]TTTTCTCCAATTAAA | 221178 |
rs529925801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087701 | ACACACGCTTCTCTA[A/G]GTCACAGAAGCTATG | 221178 |
rs529925836 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094784 | TCTAAAAATTAATAT[A/G]TAAAATATTTCAGAA | 221178 |
rs529928660 | snp | C/G | 0.000269215 | 0.0115989 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223666 | ACCCTGAAAACAACA[C/G]CATGGGCTACAGGAG | 221178 |
rs529936984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025307 | TATTCATTTTCACTG[C/T]TCTGAAGTATTTCTG | 221178 |
rs529939542 | snp | A/G | 9.59463e-05 | 0.0069256 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223080 | GCGTGTGGAAATGGA[A/G]TCTGTGGCTGCAGCC | 221178 |
rs529941657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216663 | TAAGGTATGTATATT[C/G]GGGCTAGGAAGAGGA | 221178 |
rs529954851 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012649 | CTGTTCCCTCCCCGT[C/G]TTCCGCAGCCAACCC | 221178 |
rs529964474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053932 | AGGAAGTGTTATTAT[A/G]GGGTGTCTATGTGCT | 221178 |
rs529967478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133891 | CCAGAAGAAGTGACA[G/T]CCTGCGTAGAATCAG | 221178 |
rs529985028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012987 | ACCTTCTCACCGTGA[C/T]GGCAGAGTGGGGAGC | 221178 |
rs529992107 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254957 | TAAGGATTCATGTAG[A/G]ATGGACATCATCTCA | 221178 |
rs530006928 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128905 | AAAACCTTTTTATAC[-/T]TTTTTTTTCTCACCC | 221178 |
rs530013819 | in-del | -/TAAT | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190161 | TATAACATATATATA[-/TAAT]ATATATATTATTATA | 221178 |
rs530043966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188609 | AGCCATCTCTGTAAC[A/G]TAAGTGCAGGGTGAA | 221178 |
rs530046636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088879 | CAGGAAAGCGCAAGC[A/C]AGGGCTCCTGGGTCC | 221178 |
rs530074462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047766 | GAACCAATAGAATCT[A/G]TATAGATATATGGAA | 221178 |
rs530079913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122525 | CTTCATCACTCCCCG[A/G]TTCCTCTGGTCAGTG | 221178 |
rs530102561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001634 | AGACCCACCAGGGCA[C/T]CACACTCATCCCAGT | 221178 |
rs530102835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007279 | CAGAGGAAAGGCCAG[C/G]CTAGGCCACTGCTTG | 221178 |
rs530103271 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267087 | TCCTTGTTCTATCAT[G/T]CCCCTTTCTACATTA | 221178 |
rs530103871 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194057 | CCAACTTTGCATCCA[C/T]GGTTCAGTAGCCGAG | 221178 |
rs530106368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187915 | ATCTCTATTTTAAAT[C/T]CAAAGCTAGGAATGA | 221178 |
rs530114040 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082712 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 221178 |
rs530124310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229687 | CTTCAAACAGTTAGT[A/T]TGACATCATGCTACT | 221178 |
rs530128032 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24017428 | ATCTAAATCTCTTGG[A/G]CAGAGCTTTTCTCCA | 221178 |
rs530136247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157619 | CTCCTTTTTCTGCAG[G/T]AGAGGGTGGGGCGGA | 221178 |
rs530137555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002059 | ACATCTTACATGGCC[A/G]AGAGGGAGTGACGAG | 221178 |
rs530140156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117503 | TCTGTATGACTTTAG[G/T]GATGTCAGTTTTTGA | 221178 |
rs530142418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274162 | TTTCCAGCCAATGCA[A/G]TCAGAATCCATTGCC | 221178 |
rs530149961 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198230 | GAACTCCTGACCTTG[G/T]GATCTGCCCCCCTTG | 221178 |
rs530151225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279924 | AGCCATCTTGCTTCC[A/G]CAGTGTCGCTAACTA | 221178 |
rs530152594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116783 | AGCCCCCCCCCCCCA[A/G]TGTGCTGATGTTTGG | 221178 |
rs530170562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077410 | TGATCATACTGGAAC[A/G]AAAGAACAGATATAG | 221178 |
rs530186448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163588 | CAAACATTTCTTTTT[C/T]AGTCTTTATCTTCCT | 221178 |
rs530191499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149518 | CTGAAGAGACAATCC[C/T]TGGTTGACTCTAGTG | 221178 |
rs530194285 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037758 | AGCAGAAAAATTGAT[C/T]GGAGTTTCTTAATCT | 221178 |
rs530211755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995949 | AGCTTCCTGTTTAAG[A/G]AAAGACTTGAAGAGC | 221178 |
rs530219442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203925 | ATGCTGTGGCTCTGG[A/G]TGATTAAGGTCATGT | 221178 |
rs530233553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242002 | AGGCTGCAGTGAGCA[C/T]AGATCGCGCTACTTA | 221178 |
rs530238929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279362 | AGGTCTCAAGAACTT[C/T]GGCTGTCTCCCCTGT | 221178 |
rs530253967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149831 | AACTTGAACTCGGTT[G/T]TGTGGGTGCTGAGGC | 221178 |
rs530259456 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219001 | CAAATTCTCATTATC[-/A]CCAAAAAAAAAAAAA | 221178 |
rs530263333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106631 | ACTGACAATTCGGTG[A/G]TTGTTTGTTTCCAAT | 221178 |
rs530274980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289953 | AAGTGGCTGGGCATA[A/G]TGTTTTTGTGTTAAG | 221178 |
rs530276210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284647 | CCAGCCTGGGCGACA[C/G]AGCGAGACTCCATCT | 221178 |
rs530289155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254031 | GAGGGCAGTTTGTGG[A/G]GGGAAAGGAAGAGGA | 221178 |
rs530306596 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202498 | TGTTGGCCTCAGAGA[A/C]CTGTTTGCTTTCTTT | 221178 |
rs530315359 | snp | A/C/T | 0.0111351 | 0.0739376 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144575 | ACTTTGATCAGGCAC[A/C/T]GCTGAGCAGCTCTTG | 221178 |
rs530325292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107129 | TTTACAGCTCTATCA[A/G]GTGAAGGAAATACTA | 221178 |
rs530325521 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026233 | TTCCTTTTATGATTA[A/G]TGCTTCTTGTGAGTT | 221178 |
rs530331647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169826 | GAGTCCCCACTCTCC[C/T]CTCCTGCCTGGCTGC | 221178 |
rs530333903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163121 | AAATGACCTGGCTGG[C/G]CACAGTGGCTCATGC | 221178 |
rs530346319 | snp | C/T | 0.000186956 | 0.00966658 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294914 | GCCACTCGCCCTTCC[C/T]GCACCTTTGATCTGG | 221178 |
rs530349223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134393 | CATCGAACAAGCCCC[C/T]GGCTGACTTCTTGCT | 221178 |
rs530361370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019929 | CCTGGAGTCTTTCTG[C/T]GGTTTTCAGGCCAGC | 221178 |
rs530375928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071865 | AATTTTTGAGCAAGA[C/T]GATTCTCCCCGTGTG | 221178 |
rs530376332 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104984 | TCTCATGTCCATCCT[A/T]TTAGGAGCTACTTGT | 221178 |
rs530376638 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124849 | GCAGTGGGATCAGAT[A/G]TTACTAGCATATTGT | 221178 |
rs530378618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144854 | ACCTCCTTGCCTTTG[C/T]CTTCCAGTTTCTGCT | 221178 |
rs530384247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248150 | TCTGACGCAGCCCTC[C/T]TCTCTGGCCAGGCTT | 221178 |
rs530389561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037667 | CCTGCCTCGGCCTTC[C/T]AAAGAGCTGAGATTA | 221178 |
rs530395277 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022854 | GTAGAAAAAGAAACA[-/T]TTGAATCATGAGCTG | 221178 |
rs530401230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264293 | AAAAGAAGAAGAAAG[A/G]ATATTAAAAGTCAGA | 221178 |
rs530417618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101303 | TGCACCATGAACATT[C/T]GCTATGTTGGATAAA | 221178 |
rs530422079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143990 | CAGGTGAGAAAGGCC[A/G]CCCAGGGTTGGCCAG | 221178 |
rs530438396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990741 | ATCTACCTTGTTTCC[C/T]GTGATCACCCAGAAC | 221178 |
rs530450984 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023030 | GTACCATGCTGGCCC[A/G]CTGCATCCTTCAACC | 221178 |
rs530454613 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989459 | AGTTATCTTTTAAAA[C/G]TTGAATACATAAACG | 221178 |
rs530460485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174581 | TTTATTTTATTTTTT[A/G]TTATCACTTTTTTGA | 221178 |
rs530473911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253494 | ATTTAAGCAACACAT[C/T]CCTACCAGAATGGCA | 221178 |
rs530479700 | snp | C/G | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304398 | CCTGGACAGGAGATG[C/G]TGTGTTAAACTGTTA | 221178 |
rs530499733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240462 | TGGTTTTGGGGTCAC[A/G]GTGGTGACACGTGTC | 221178 |
rs530511561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995789 | AACGTGTAGAGAATG[A/G]TGAGAAGGGCATAAA | 221178 |
rs530537705 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085413 | ATTACAGGTGTGAGC[C/T]ACCGCGTCCAGCTTC | 221178 |
rs530540083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139779 | GTTTTAAAATCTGTA[A/G]CATGCAGGCCGGGCG | 221178 |
rs530550018 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24302513 | TGAGAACTTGGACTT[A/G]GAGTCTCAGCATTTT | 221178 |
rs530558972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982942 | CAAGGCTGCTCTGCC[A/G]TCTGGGAAGAAGGTG | 221178 |
rs530566557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993260 | GAGCATCGCTGATCA[G/T]CCCAGTTACATCTGT | 221178 |
rs530620287 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147082 | TAACTCCAAGCATGC[A/G]TTGGATGGAAGATGA | 221178 |
rs530623144 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095396 | GAAATAGAAGGGTGG[G/T]TACCCAGGGCTGGGG | 221178 |
rs530623244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255103 | CAGGAGTGCGCACGA[A/G]CTAAATCCTTGCCTT | 221178 |
rs530624598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282553 | TTGGCCTCCCAACAT[A/G]GATCTCAGTTCCTGA | 221178 |
rs530634400 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054687 | TAATAGTAGCGCACC[A/G]TTAATTTATGATGGT | 221178 |
rs530635630 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159604 | AGATGAACTAAGTCC[A/C]TTACTTACAGGAGGC | 221178 |
rs530653123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196776 | CAGCCTAGTACATGT[C/T]GGGCACTTAGTGTTC | 221178 |
rs530653651 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096220 | TCACGTGGAGCTTAT[-/A]AGTCTCGGGAGGATA | 221178 |
rs530658069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200463 | TGCGCAACCTGAAAC[A/G]TGAAATGCTACCATT | 221178 |
rs530658556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207349 | GGTAACAAATCTGCA[C/T]ATCCCGCACATGTAC | 221178 |
rs530666310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101080 | CTCAAGGGGAAATTC[A/G]CATACACTTGAGTGT | 221178 |
rs530667247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128289 | TGGGACAGGAAAGGA[C/T]ATTGTGGCTTCATCA | 221178 |
rs530679275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246015 | CCTGTACCCAGCATC[C/T]GTCACTGCCTGGAGT | 221178 |
rs530696225 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24130969 | ACAGGGGTGGAGCGG[C/G]GGACGCTTTCTGGCT | 221178 |
rs530710229 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109171 | TGTCCAAGTGTTCTC[A/T]TTGTTCAGTTCCCAC | 221178 |
rs530711092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127876 | TTCATTTATTTCTTA[C/G]TCTTCCTACCGAATT | 221178 |
rs530717223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206938 | TGTTCTTTGCAGCAC[C/T]ATTCACAATAGCAAA | 221178 |
rs530728505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048668 | TTTAGAGTCATCAGT[A/C]TCTGATCAAAATTAA | 221178 |
rs530742187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167158 | GTGAGGATTCCATGA[A/G]TTGATCCTTGTAAAA | 221178 |
rs530742303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086389 | GGGTCCTCTTAGGAG[A/G]ACCCATCTGCTTGGG | 221178 |
rs530751080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013184 | GCTTAGAGCTCTTCC[C/T]GTCTCCCCACGCGTG | 221178 |
rs530757032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281531 | ACAGGTGCGGACCCA[C/T]GGGCCATGCCTCAAT | 221178 |
rs530760013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007328 | CTTGCCTGTGGAGGG[A/G]ACTGGGCTCAGTGAG | 221178 |
rs530761836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251221 | AGCTCCACAAATCCT[A/T]ACTGAGGGCTCATCT | 221178 |
rs530777482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113019 | TCTGGCTTCCTGGAA[A/G]CCTAGGTTCCCAGGC | 221178 |
rs530793503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006836 | TTTTACTCTAAGAGC[A/G]CAGGGAAGCCACGTC | 221178 |
rs530804472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166552 | CAAGCACATCAGTCA[C/T]GACTGAGTCTGTGTG | 221178 |
rs530824349 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977914 | TTTATTTATTTATTT[A/T]TTTTTTTGAGACAGG | 221178 |
rs530849894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292595 | TTTCTATGGCAAACC[A/G]CAACAGTTCTGGGTT | 221178 |
rs530863582 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036365 | GCCATGGCTGAAGTA[A/G]AGGAAGAATGTCTGG | 221178 |
rs530876015 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257113 | TCTGTTTATGTTGAT[C/T]AGAAGTCAAATTCGA | 221178 |
rs530878307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150318 | TGCTGCACAGCTCCT[G/T]CCAGTCCCCTAGAGA | 221178 |
rs530882203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177823 | CCTTCTAAAGGCCCT[A/G]TCTTTCAATATAATC | 221178 |
rs530884502 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192128 | CCCCCAGTCCATTGT[-/G]GGCCATGCTCAGACA | 221178 |
rs530885733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078090 | CACTTGATGCCTGCT[C/T]TCCTCCTGCACGTGT | 221178 |
rs530895366 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303314 | CGTGGGGCTGACCAC[A/G]GTGTTCCCTGGCATC | 221178 |
rs530898059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122784 | AGGGGAAGTAGCTGC[C/T]ACATCTGTGGAGACT | 221178 |
rs530902729 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218708 | AAAACATTATGAGGG[G/T]TTTTTTTTTTTGCGA | 221178 |
rs530906742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112940 | GAATTCTACTGATTT[A/G]TAATTCATTCTAGCA | 221178 |
rs530907840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117510 | GACTTTAGTGATGTC[A/G]GTTTTTGATTCATTC | 221178 |
rs530913272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256781 | TAGGCTACTGGGTGT[G/T]TTATTTGGGATAATA | 221178 |
rs530915034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997293 | CACAATCAAAACCAT[A/G]TCCATATTCATCACC | 221178 |
rs530936718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178218 | TCCAGAAGGCGCAAA[C/T]GTTCCAATAATAACA | 221178 |
rs530941082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149945 | CATCCAGGGGCTGTC[A/G]GGGAGGGAGAGAGCT | 221178 |
rs530951467 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051970 | TGGCTCTGGTCCTCC[C/T]ACCTCATCTGTGCAC | 221178 |
rs530958922 | snp | G/T | 0.000676819 | 0.0183835 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224482 | CAGGGCCTGTGTCCT[G/T]GCAGGATCCCCTGGA | 221178 |
rs530960300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219312 | AGCACACAACAATCA[C/T]GTTGTTCAGCTCAGG | 221178 |
rs530982499 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303005 | CTACACAGAAACACC[C/T]GTGACCCACTATGAG | 221178 |
rs530985620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071519 | AATAAAGTACCTCAC[C/G]CTGTATCCTCAATCG | 221178 |
rs531001646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038208 | ATGAGCCACCGCGCC[C/T]GGCCAACTAGGCTAG | 221178 |
rs531008568 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189626 | ATTTAATTTATTATA[A/T]AAATATATATATTTA | 221178 |
rs531012017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066785 | GCTCAGGTTGACAAT[A/G]CCAACTGCACAGTCA | 221178 |
rs531014159 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026776 | TGGAGACGGGTTTTC[A/G]CCGTGTTAGCCAGGA | 221178 |
rs531022931 | in-del | -/A | 0.420733 | 0.18262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219004 | ATTCTCATTATCACC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs531027621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225212 | CAGGAATGGAGCAGC[A/G]AGGGGTGTGTGAGTG | 221178 |
rs531042726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984945 | TCTGTGTAACCGGCC[A/G]GCGTGCACATCACAT | 221178 |
rs531059480 | in-del | -/GAAAA | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120582 | CCACTATACCACCCT[-/GAAAA]CTGCCTCTGTTTTCT | 221178 |
rs531066865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262231 | TACTGAAACTTATTT[C/T]TTTGAAAAGTCTTGT | 221178 |
rs531072078 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189244 | TGGGAGGCCGAGGCC[A/G]GTGGATCACGACGTC | 221178 |
rs531072166 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195240 | GCTTCTTTTACTTAG[A/G]TAATATTTTCAGTGT | 221178 |
rs531092271 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24206353 | AATGCAAATCAAAAC[C/T]AGAATGAGATACCAT | 221178 |
rs531114859 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280942 | AGTCACCATGCGTTG[G/T]TCAGGCTCCCGTGTT | 221178 |
rs531121181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145584 | TGCCTGAATAACAGC[A/G]TTTGTGTAGCTAGAT | 221178 |
rs531133693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194613 | GCTGCATAATGAGCC[C/T]GGTAGGTCCTCATTG | 221178 |
rs531142552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231399 | TGAGCAAAACCTTGT[C/T]TTCAAGGTTTGTCCA | 221178 |
rs531153455 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24204321 | AACGATAGGAAAATT[A/G]TGAATCTTCCTGAAT | 221178 |
rs531158249 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172476 | GTTTTTTTCTAAAAC[G/T]TTCGTGGTTTTTCAT | 221178 |
rs531170060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295305 | ACCTCATAGGCTACC[A/G]TGAGCATTTTATAAA | 221178 |
rs531175969 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209754 | CGTCTTTTTGAGGTG[A/T]TGATTTCGTTTTTTT | 221178 |
rs531186884 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24087173 | GAAACCTGGCAATGT[C/T]ACCACTCCCAGAGCC | 221178 |
rs531193055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061237 | CAGCTTCTTGCAAGG[C/T]TGTAGAGAAAAAATG | 221178 |
rs531194391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134813 | GGACAGAATGTGTCC[C/T]CCAAAATTTTGCATG | 221178 |
rs531215303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096179 | TTCTGGAGCTAAACC[A/C]AAGAACAAAACAGAC | 221178 |
rs531219485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080291 | GCTGTAAACAAATGG[A/C]TCAGGACATCACAGC | 221178 |
rs531228006 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158859 | GGGCTTGTACAGGGC[C/T]TCAAGGATGCGGGGG | 221178 |
rs531239290 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24018623 | GGCACAGCTAATTGG[C/T]GAGGTGAGCGCTGCT | 221178 |
rs531250358 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157490 | ATTTTTAGTAGAGAC[-/G]GGGGTTTCACCGTGT | 221178 |
rs531254907 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24065944 | TAATCTGAGCTACAT[A/G]TTGTCACAGGGAAAC | 221178 |
rs531259071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259787 | CGAAACCTTTCTGAA[C/T]TGGATTTTATTTTAT | 221178 |
rs531262767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021249 | GAGTATTCCAAGTGC[A/G]GAGCACAGCATAAGG | 221178 |
rs531277287 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245025 | GCTCTGGCATGGCCG[G/T]GGGAGAGGGCAGGTC | 221178 |
rs531294121 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301009 | CCTAATCTCCATGCA[A/C]ATTAGAATTCCCTGG | 221178 |
rs531295704 | in-del | -/TAAATAAATAAATAAATAAATAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202091 | AAATAAATAAATAAA[-/TAAATAAATAAATAAATAAATAAA]AAGTGACTCTGACAT | 221178 |
rs531301105 | in-del | -/CT | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188114 | GGAGGCCAAGGCGGG[-/CT]CAGATTGCCTGAGCT | 221178 |
rs531304298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125558 | AAAATTCACCAACCA[A/G]GTGGTTTAAGGAGCG | 221178 |
rs531306065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000166 | TACAGAATGTCAGCT[A/G]TGGTGGTCTAGAAAG | 221178 |
rs531311741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993115 | TCCACAGTCTAAGTC[A/G]CTACATAAGGAGCAA | 221178 |
rs531344060 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248226 | TGGGAATGGTTACTC[C/T]ATGGCCCAGCTTTTT | 221178 |
rs531348155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254113 | GCAGTGACCACAAAA[G/T]CCATCCCCATTTTCC | 221178 |
rs531362273 | snp | A/G | 0.000337781 | 0.0129914 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162390 | GCTGCGGTTTTCCAT[A/G]CTCCATCAGCATCCC | 221178 |
rs531368654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120726 | CAAAAGCTTAAAATC[A/G]AAATTAAGGTATCCT | 221178 |
rs531375968 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045899 | CCTCATTTCCCTAAT[C/G]TGGAGAATGGGATCA | 221178 |
rs531377245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205542 | CAATGCTATTCTGAT[A/T]AAATTACCATTAACA | 221178 |
rs531383528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274070 | AGGCGGAGAGGTCAG[C/T]GTGGACGGATGGAAG | 221178 |
rs531395905 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24073532 | GAGTGGCAGTCTGTC[C/G]TCACACACAGGTGAC | 221178 |
rs531414781 | in-del | -/CTTA | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980621 | TCGTTTTGAGACAGT[-/CTTA]CTTTGTCGCCCAGGT | 221178 |
rs531420453 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104103 | ATAAAACTGTTAGAG[A/C]GCTGTAGATGACACG | 221178 |
rs531426207 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184441 | GGTCACCAGCAGATA[A/C]CCTCATTTGGATGGA | 221178 |
rs531427606 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215149 | GCTCCAGGGACCCCT[C/G]TTCAGGAGGAGTAGC | 221178 |
rs531429649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115245 | TCTCACAGCAGCAGT[C/T]ATGGCAGCAGTGACT | 221178 |
rs531434671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110559 | ACTGCCTCCTAAGGC[A/G]GTGGAGAAGCAGGGT | 221178 |
rs531464252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137651 | CTAATCCCAGCTACT[A/T]GTGCGGCTGAGACAG | 221178 |
rs531466559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193013 | AAGGTTTTGAGAGAA[A/G]TTGAAAGTCAAGGTG | 221178 |
rs531469816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074655 | AAAAAAAAACCCTTG[C/T]AGGAATTAGGGAACT | 221178 |
rs531471013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273457 | CACATGTTTAAAAGA[C/T]TGAAAAATACTATTT | 221178 |
rs531483454 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198469 | GAGTCTAGAGGTCTC[A/C]AAAACCCTTTGCCAT | 221178 |
rs531486089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229465 | CTTCATCTGCCCCTG[C/G]GGATGGTAAGAGCCA | 221178 |
rs531489593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023198 | TGGTTTTCTGTCTTT[G/T]TGATAGGTTGCTCAG | 221178 |
rs531490199 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185956 | CTTATGGCAATCTTA[A/C]GGCCAAATTTCTTTC | 221178 |
rs531498170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035784 | TTTAGGAGGCCAAGG[C/T]GGGTGGATCACTTGA | 221178 |
rs531499446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156760 | TTATTACACTTAATT[G/T]TCACCATAAGATATC | 221178 |
rs531499497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140922 | GGCTCACGCCTGTAA[C/T]GCCAGCACTTTGGGA | 221178 |
rs531514153 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24004533 | GCAGACGGGACTCAG[A/G]GAGGGTAGGGCTGCC | 221178 |
rs531529988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142190 | GTGCCCCCCTCCCCC[A/G]CCAATATTAACATCT | 221178 |
rs531537060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024014 | GCAATAGTCCATGAC[A/G]GTGGTGAATAAGTTG | 221178 |
rs531543721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306254 | AGCCAGCTGAACCAG[C/T]ATTTTATCAGGTGGA | 221178 |
rs531545815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241755 | GCAGCTTTAGACAGA[A/C]AGATTATTCCACCAG | 221178 |
rs531552320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228826 | GTGTTATTTAAAATA[A/C]ATATTATAATGTACT | 221178 |
rs531586007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278097 | AAGGAAGGGTTAGTG[A/T]GGGAACGGAGGGCAG | 221178 |
rs531597365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142651 | ACTTTTTTCCTCCTC[C/T]CCCTTTCCTCTTCCT | 221178 |
rs531600403 | snp | A/C/G | 1.672e-05 | 0.00289132 | missense | SPATA13 | GRCh38.p7 | 13:24284182 | TTAGTGGATGACAAC[A/C/G]GTAGTGAGGAGGACT | 221178 |
rs531608624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248030 | GTCCTCCCTGGGCCC[A/G]TGGCCTGACTGACAG | 221178 |
rs531617541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162143 | TTGTCTTATTATCCC[A/G]TATCCTAATTCTCAT | 221178 |
rs531638025 | snp | A/G/T | 0.000132283 | 0.00813183 | missense | SPATA13 | GRCh38.p7 | 13:24289018 | ATATCCGACAGTGCC[A/G/T]CAAGCACACAGGAAT | 221178 |
rs531651267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981325 | GAGCAGTTTTTTTGT[A/G]GCTACAATAGTACTT | 221178 |
rs531655469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192478 | ACCCGCTGAAACAGC[A/G]TCTTCCTCAGAATAC | 221178 |
rs531657709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138180 | GGCGTGGTGACGTGT[A/G]CCTGTAATCCCAGCT | 221178 |
rs531658075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132912 | CCTGGGGGGTGGAGA[C/T]TGCAATGGGCCAAGA | 221178 |
rs531676309 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168519 | ATTTTTTTCTGCTGC[A/T]GAATCACTAAGCAAA | 221178 |
rs531689124 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156298 | GGACAGCGTGAGACC[A/G]TTTATTCTCCTCTTT | 221178 |
rs531698731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121421 | TTTTGCTATTTTATA[C/T]ATAGGCTAGCAGGCT | 221178 |
rs531698756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126935 | CTAGAGATCATAATG[A/G]GAAGACTGGAGATTG | 221178 |
rs531718935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132388 | TTATGCTGTACTCCA[A/G]TATATCAGACCCTGG | 221178 |
rs531729601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059004 | TGAGACGGAGTCTTG[C/T]TCTGTCACCCAGGCT | 221178 |
rs531736995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167945 | CTGTGGAGACATAAA[A/C]ATGTTTCTCTCTCTG | 221178 |
rs531750643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012459 | TCTAGTACAACAGGA[C/T]AGAGACAAAGGCTGT | 221178 |
rs531756594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241245 | TAACCCAGTAAATGA[A/T]GTTTCTACTTCCAGT | 221178 |
rs531758523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121788 | GATTTCCACAGTGTC[A/C]CTTTGAAGCTTCACA | 221178 |
rs531758804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283532 | GAAAATCTGACTAGC[A/G]GGGTGGCCAATCTAA | 221178 |
rs531761089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052701 | TGTCTAAATTTCTCA[A/G]TAAAAGGCATATTTT | 221178 |
rs531767419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047077 | GGGGATGAAATTGTA[A/G]GGGTGTGGAAAATGG | 221178 |
rs531779275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214266 | ACCTAAGGCCAGATG[C/T]ATGTACAATAAACTT | 221178 |
rs531781949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011920 | CTTTAAACTTGCAGC[A/G]GAGGCTTCAATGTGC | 221178 |
rs531789858 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24287957 | GAAGACAGGTTGAAG[G/T]CAGAGAACTGCCCGT | 221178 |
rs531801655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252235 | GGCTGCTTTCCTTGC[A/G]TCTGGTGCCCTCAGT | 221178 |
rs531805881 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111580 | CCTGGCTAACTTGTA[-/T]TTTTTTGTAGAGATG | 221178 |
rs531825300 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087015 | ACGTTTTCTTTTTTT[A/T]ATAAAGCAGAACAGC | 221178 |
rs531833708 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23994526 | GGCATGACTGCAGGT[C/G]CCTTTCAGGCCCTGG | 221178 |
rs531848203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288610 | CACAGAGCTGCATGG[C/G]CTATTCAGCAAGCAG | 221178 |
rs531854365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148418 | CAGAAATGGCCATAG[C/G]GTTGGAATAAATAGG | 221178 |
rs531863406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265323 | CCTGTGTTACGTTCA[A/G]TGCCTTTCAGGTTCC | 221178 |
rs531871973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005561 | GGCCATTATACAGCT[G/T]TCTTCCCTGGTAAAG | 221178 |
rs531880358 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011318 | CTGAGGCAGTGCCGG[C/G]CGGCTTGGCCATCTC | 221178 |
rs531882300 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029934 | TCCAGCTCCATCCAT[G/T]TTCATGCAAAGGACA | 221178 |
rs531900552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294018 | GCCCCGCATTATTAA[C/T]GCTGAGCAAAACCTG | 221178 |
rs531907285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116722 | GGGTTCACCATTGCC[A/G]TAGACTTAACTGTGT | 221178 |
rs531919296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000739 | GGGAGAGCTCTGGGT[C/T]AGAGGCATGAATTTG | 221178 |
rs531930775 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24266309 | ATTTTTATAGAGATA[A/C]TGTCTTGCTCTGTCA | 221178 |
rs531941154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151553 | AAGTCCTGTCTCTGT[C/G]AGGGTTTTGTAATAA | 221178 |
rs531949391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076606 | ACTGAGGGTCTTGTG[A/G]CTCTGGTGACCCGGG | 221178 |
rs531950116 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24183467 | TAAGTTTTCCAAGAG[A/G]TACAAGTCAAGGCTT | 221178 |
rs531957277 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067847 | ATAGCTGGGACTACA[G/T]GTGCCTGCCATCACA | 221178 |
rs531964837 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156256 | TTTTTGAGGAATTGC[A/C]ATACCTGTTGTCCAC | 221178 |
rs531969309 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081319 | TGAGGCCCTTCTCTT[A/T]TTTTATTTTATTTTA | 221178 |
rs531974908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158375 | GCTTTTACACAGAGG[C/T]CACATTGTGATTCCC | 221178 |
rs531994227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195320 | AATAATATTCAATTA[C/T]GTGGATATCAAATTT | 221178 |
rs532002547 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135086 | GCCTTCAGAAAGAAA[C/T]AGCCCTGCCAATGCC | 221178 |
rs532024492 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220555 | GTTGAACTTACTTTG[C/T]AACTGGTTACAGGCT | 221178 |
rs532026799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111461 | CACCGAGGCTGAAGT[A/G]CAGTGGTGCAATCAC | 221178 |
rs532032528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075261 | TAATCTCCCACTAAA[A/T]TATCAGTTCTATGAA | 221178 |
rs532034213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237847 | TTATATATGTATATA[A/T]AAAATATATCACATA | 221178 |
rs532047180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993684 | ATAAGTGAGAATTTA[C/T]CTAGGAAAGCCCATC | 221178 |
rs532050829 | in-del | -/TATATATATAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024959 | AAATATATATATAAA[-/TATATATATAAA]CACAGATGAAGCATA | 221178 |
rs532060700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165883 | GTGATGTAGAGATTG[G/T]TAAATGTGCCCTGAG | 221178 |
rs532072344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264784 | AGGATGAAAAATCCA[C/T]GTGTGCTTACAGAGA | 221178 |
rs532075229 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147975 | TATGTATACACCACA[A/T]TTTTTTAATCCATTC | 221178 |
rs532078276 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185893 | AAATAAGCAGGGTAG[A/G]TCAGTAGGCTGGAGT | 221178 |
rs532083744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000705 | ATTCAGGAAAGCCTT[C/G]GGTTAGAGGTGTGAA | 221178 |
rs532084913 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987687 | AGTTCAGCGGCATTC[A/G]GCACATTCACATTAT | 221178 |
rs532084983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994089 | GTTCTTGCCAGTGAC[A/G]GATATTCTTGTCATT | 221178 |
rs532085417 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040968 | AGACTCAGGGGGAAC[G/T]AACAATGAGGCCAGG | 221178 |
rs532091940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238583 | CAGGAAAGAAAGCCA[C/T]CTTGGACTCCAGGGT | 221178 |
rs532103684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250638 | CTAGTACTGGATTGT[A/G]TACGTCTACATTTTT | 221178 |
rs532110077 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176490 | GTCACAGTTTCCTTT[C/T]AATTTCTGCTTTTCA | 221178 |
rs532120257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000225 | CAACAGAGGGCTTGA[C/T]CTGGCCTAGGGGCTG | 221178 |
rs532120479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115350 | CCACAGACTGGCACT[A/G]GTCCATGGCTTGTTA | 221178 |
rs532124223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281474 | GTTCCCTGGCTGTCG[C/T]GGTGTCCGGCGCACC | 221178 |
rs532158860 | snp | C/T | 6.61802e-05 | 0.00575202 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24286797 | AGAGCTGTCGGAAAA[C/T]TCCAGCAGCACCCCC | 221178 |
rs532161376 | snp | A/T | 0.000119682 | 0.00773476 | utr-variant-5-prime, missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24222912 | CTGCGGTCTGCGGAC[A/T]CGGCAGTGCCCGTGG | 221178 |
rs532170492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988142 | TAGAGACGGGGTTTC[A/G]CTGTGTTGGCCAGGC | 221178 |
rs532174348 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24018110 | AATCACGAGTCTTAC[A/G]TTTTAAGATACTTTA | 221178 |
rs532181932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115661 | GTTTACAACCGCAAT[A/G]AACATTCATCATCCC | 221178 |
rs532186225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035887 | GGTGATCATGGCTCA[C/T]GCCTGTAGTCCCAGC | 221178 |
rs532189871 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062106 | CACCCATGGGGGTAT[C/T]TTGAGGAACACACTC | 221178 |
rs532191113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099266 | TGAGCATCTCTTTAT[A/G]ATATCATTCTATCTA | 221178 |
rs532191204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250041 | GTTTGGATGCCTTTT[G/T]CTAATCTTTCTTTCC | 221178 |
rs532199814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147657 | TCTTAACCATGTTTA[A/G]GTCTATTAAGTACAT | 221178 |
rs532218433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171024 | AGCATGGAACACATT[C/G]CTCCATGCCCCTTCT | 221178 |
rs532218970 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23990153 | GTTGAGATGCCACCC[A/G]ATCCCTGCTGGATTC | 221178 |
rs532222134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104989 | TGTCCATCCTTTTAG[A/G]AGCTACTTGTCATCT | 221178 |
rs532223937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036664 | CTTGTCTAAAACTTC[A/G]CAATTCTGTGAGATC | 221178 |
rs532233361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110606 | ATTTGTTATTCATTC[A/C]TCAAACCTTGAGCAA | 221178 |
rs532242853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064999 | CAGGCCACAGGAGCC[A/G]GGATAATGAAATGCA | 221178 |
rs532247996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069819 | ATTTGTACATAATCT[A/G]AGACCAAATGGCACT | 221178 |
rs532251480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093371 | TTAAGCTTGCAAACA[C/T]TCTATCACCATTTGC | 221178 |
rs532251540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099711 | GATGAGCGCCATGTG[A/T]TCAGTGTCATGAATA | 221178 |
rs532278857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171390 | TGGAGTGAGGAGAAC[G/T]GGTGCTGGGAATGCT | 221178 |
rs532293269 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982168 | TATTAACTTTTTAAA[-/T]TTTTTTGTCAGATTT | 221178 |
rs532305356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011954 | TCCGCCTCCCCCTAC[A/G]GATTGTAAAACTCAC | 221178 |
rs532310855 | in-del | -/TC | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24036694 | CATAGACAAATTGCA[-/TC]TCTTCTGTGAAGGCT | 221178 |
rs532315253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029951 | TCATGCAAAGGACAT[C/G]ATCTAATTCTTTTTT | 221178 |
rs532320061 | in-del | -/GAAACAT | 0.00119737 | 0.0244387 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253810 | CCCAAAGACAGGCAG[-/GAAACAT]GATGTGTCTGAGGTT | 221178 |
rs532327778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205626 | AGCCTGAATAGTGAA[A/G]ACAATTCTAAGCAAA | 221178 |
rs532340199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138261 | GCAGTAAGCTGGGAT[G/T]CACCATTCCAGTCCA | 221178 |
rs532341664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024082 | ACTGTGCTGAAGAGG[C/G]TCTGAGTCATGTGCT | 221178 |
rs532364428 | in-del | -/ACAA | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158681 | TATTTTTTAAAACTC[-/ACAA]ACAAACAATCAGCAA | 221178 |
rs532383246 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059097 | CTGCCTCAGCCTTCC[A/C/G]AGTAGCTGGGACTAC | 221178 |
rs532387887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262034 | TATGAATGTGTCAGC[A/G]TTTATTCTCACTGAA | 221178 |
rs532397277 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013178 | AAACGGGCTTAGAGC[G/T]CTTCCTGTCTCCCCA | 221178 |
rs532423445 | snp | C/T | 3.30732e-05 | 0.00406638 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302793 | AGGAGGCTGTGCTTC[C/T]ATGGAGCTGGGTGTC | 221178 |
rs532424019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296162 | ATTGGAGAGAAACAC[A/G]TACATTTCAAGGGCC | 221178 |
rs532424594 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181219 | GCTGTTCGCTGCTCT[A/C]AACTTTAGAAATACT | 221178 |
rs532463116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088356 | ATTAGAACATAAACC[C/T]AGCTGACTTCAAGTT | 221178 |
rs532469749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116330 | ATGACTCATCACTCC[A/G]CAAAGGCCCACCTCC | 221178 |
rs532471643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122198 | TCAGCCAGCATTGCT[A/G]TATACTGTAACTGTT | 221178 |
rs532474072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059343 | GTCACAAAAAAAAAA[C/G]GCTTGTCTTTGATCT | 221178 |
rs532480585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183525 | CCACGGCTCACGGGC[C/T]ACATGCAGCCCAAGA | 221178 |
rs532484922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047659 | CCAATATAGTGTGGG[A/G]GTTCTTCTTTATCAT | 221178 |
rs532497946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291291 | TACCCTTGAGGTTGA[C/T]GTACAGCAGCTCGGC | 221178 |
rs532501109 | in-del | -/CTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046859 | GATCCTTCTTGACCA[-/CTG]CAGAGATAAAATCAG | 221178 |
rs532514257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006645 | GGCTGATTTGGTCAC[C/T]ACAGTTGTCTTAGGG | 221178 |
rs532529043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082548 | ATCTTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 221178 |
rs532538262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087675 | CATGGCATCTTTCAT[C/T]CCCTCTCTACACACA | 221178 |
rs532538987 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037356 | TTAAAGTATAATTTT[A/T]AAAAAATTAAAAAAA | 221178 |
rs532546006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189213 | GTGGTGGCTCATGCC[G/T]GTAATCCCAGCACTT | 221178 |
rs532568892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042537 | CCACCACCGTGGACT[A/G]ACTCACATCTCAGAG | 221178 |
rs532606453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268021 | CCAGTCATGCTGATA[A/C]TGCTGGTCCATGGGC | 221178 |
rs532607688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188661 | GCTGAAGCAAGTTCT[G/T]CAGAAGATCTAGCTA | 221178 |
rs532638245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237085 | TGCTGCAGGCTGGGC[A/G]CAGGGCTCACGTCTG | 221178 |
rs532640268 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029239 | TCTGAAAATCTTTTC[A/G]TGGGAATACTTTAAA | 221178 |
rs532662307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031563 | ATGGCCTTTGAGCCA[A/T]GAAAAATCTGGTGAA | 221178 |
rs532669126 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995846 | AACTGGGGAAGGGTG[A/G]GGCTGCCTTGAACTG | 221178 |
rs532671972 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203989 | CAGTCATGCAAAAAT[G/T]TAACTTAATGTAATG | 221178 |
rs532684326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001192 | TACATTTTAAGGTTA[C/T]AGTAGAGCAGAAGTA | 221178 |
rs532684569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076229 | TTAAGAACTGCCACA[A/G]GTGCAGTTCTTAAAA | 221178 |
rs532690123 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268368 | CTTTTGAGCCTATAA[-/T]TTAATAAACTACCAC | 221178 |
rs532697813 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139527 | AGGTTTATTACCATC[A/T]GTTATATTAAGGTGC | 221178 |
rs532710799 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157670 | AGGAGCTCCTCAAAG[A/G]AAAAAAACTGAAATG | 221178 |
rs532723902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144423 | TAACATCACTCAGCA[C/T]CTTCTGTGTTCCAGG | 221178 |
rs532742544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149381 | GGGGTGAAATACGCA[A/T]CTCACTGTGGGCTGT | 221178 |
rs532745964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076619 | TGGCTCTGGTGACCC[A/G]GGGTCTGGGGTGGTG | 221178 |
rs532773037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164316 | TGGACTCCCACTGAG[C/T]CCCCTTGCTCCTGCC | 221178 |
rs532777536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129372 | CCATGTTTCAGGATG[A/G]AAAAAAATTGCCAAA | 221178 |
rs532784401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131439 | CCTGGGCACTGAAGC[A/G]CCTTATCTTGTTTAC | 221178 |
rs532786721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198244 | GTGATCTGCCCCCCT[C/T]GGCCTCCCAAAGTGC | 221178 |
rs532788392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015254 | ATGAATAGATACAAA[A/C]AGTCTTATAAGCAAA | 221178 |
rs532789593 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140341 | AGGAAATCAGTTCAT[A/C]GTTTGTTGCCCCAGC | 221178 |
rs532795386 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090404 | CCTTCTAGATGCCCC[A/G]CAAACACCTCAAACA | 221178 |
rs532802093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220635 | TCATCCAAATGTAAC[C/T]CCCAGCTCCTCTGGC | 221178 |
rs532812362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123481 | TCAGAAGTATTTCAG[C/T]GAAAGAGCCAATCAT | 221178 |
rs532817271 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24121247 | TTTAGCAGCAATGAA[A/G]TACCACTAAACCCTT | 221178 |
rs532824801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170384 | CATTTTTGTTGATGT[C/T]CTACCATAGGAGTCT | 221178 |
rs532826716 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242614 | TACGTCTTCTTTGCT[G/T]CTTTGAAAATATAAT | 221178 |
rs532835435 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220173 | GTTGGTACCTCTTCC[C/T]CTGTAGACAGCACTG | 221178 |
rs532843685 | snp | A/C | 0.000495417 | 0.015731 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249433 | GTTCTTTCTTTAATA[A/C]CTTCCTGGATATTGA | 221178 |
rs532858758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226992 | GACTATTGAGAACCG[C/T]CTGCTCATTTGCATA | 221178 |
rs532862037 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24060731 | CTGTAAGGAACTTAA[A/G]CAAATTTAGAAGAGA | 221178 |
rs532868459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989580 | GAAAACTCAAACTCA[A/G]CATGCCCCACTCTGA | 221178 |
rs532875461 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119060 | GCAGGCGCCTGCCAC[C/T]GCTCCCTGCTAATTT | 221178 |
rs532878084 | snp | G/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304848 | TGGCATGTGTGGGGG[G/T]GTGTGTGTGTATGTT | 221178 |
rs532896764 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978872 | ACTAATTAAAAAAAT[A/T]TTTTTTTTTGGTAGA | 221178 |
rs532905074 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299725 | AGGAGGAAGGCTTCC[C/T]GCGGGAGAAGGCAGG | 221178 |
rs532917070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039050 | CGATTAAAAAAGTTA[C/T]TGTTTACACCACCAC | 221178 |
rs532932034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099991 | CTGGCCCAGGGTCCA[C/T]GGAGGGGCTTCTGGT | 221178 |
rs532945652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056437 | TGTTATTCCATTTCC[A/G]TACAAGACATATGAT | 221178 |
rs532955440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197225 | TATTTATGTGATGGA[A/T]TAGTCAAGTATAAAA | 221178 |
rs532970354 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23991726 | ACCAAGAGGACAACA[G/T]AGTAATCATCCCACA | 221178 |
rs532973557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295138 | TCGTAGAGGGAGTAC[C/T]GTGGGAACAGTAGAG | 221178 |
rs532977337 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212744 | CACTTTGCCAGATAT[C/T]GAAAAAAAGAAAGGC | 221178 |
rs532987281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152447 | CTCTGTCTGACACCC[A/G]TCCTGTCACATTGTG | 221178 |
rs533015447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201653 | ACCATGTTGGCCAAA[A/G]TGGTCTTGATCTCTT | 221178 |
rs533015722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114356 | CTAATTCAGTGTGCA[A/C]GTGTGTGCCTGCATG | 221178 |
rs533025555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272787 | ACATCTTTGAGCCAC[C/G]GTTTCCTCCTTCATA | 221178 |
rs533029861 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264977 | GGGGTTCATTGAAGC[C/T]GCTGAGAGCACATAT | 221178 |
rs533047901 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24008208 | AAAGAGATTTCAGTC[A/G]CCTAAAGCTCTTGAT | 221178 |
rs533060071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050411 | CAGATATCCTTGTTA[C/T]AAGAGGAGAGCATCA | 221178 |
rs533062603 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167730 | CTTCTGTGGCAAGTG[A/T]TCTGTCTTCTAGGGT | 221178 |
rs533069080 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272438 | ATACTGAGTGAATAC[A/G]TGTAATAAAATGACA | 221178 |
rs533078223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191757 | CCTTGTGATCCGCCC[A/G]CCTCAGTCTCCCAAA | 221178 |
rs533081741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287799 | CACCTGAAAGGTTTT[G/T]TCTTCCTGTGGTATT | 221178 |
rs533083765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277216 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGGT | 221178 |
rs533101071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044750 | GTCATTTGCAATGTG[A/G]ATGAACCTAGAGGAC | 221178 |
rs533119452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293461 | CTGGGTCCAGAAGTC[C/T]ACACCTCACTCTTCA | 221178 |
rs533119510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287408 | ACTGAAGCACTTTTC[C/T]TGCCTTGATTTCTCA | 221178 |
rs533120479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155626 | TGCAAAATCCCAATG[A/G]CTTTCTGCAGATTCT | 221178 |
rs533128922 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029029 | TTTCCTCGTATGTGG[-/T]TTTTTTGTTGTTATA | 221178 |
rs533148033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998116 | GTCATGTGATATGTA[A/C]GTTTAACTTTTTTAG | 221178 |
rs533154766 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057129 | GTACATGTGCACAAT[A/G]TGCAGGTTTGTTACA | 221178 |
rs533169306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986179 | TAGGTATTTCGGCTC[G/T]CCCAGGGACCTAGTC | 221178 |
rs533172485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240526 | ACAGGACATGGTCAC[A/G]GGCTGGGATGGAGTT | 221178 |
rs533185361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160951 | AGACGGCTTCGGGCG[C/T]GCGGCTCTGCCGGGC | 221178 |
rs533185384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154842 | CTTCTTTGGAGCTGT[A/G]TGACTGATAGACCAG | 221178 |
rs533202892 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979717 | TGGGCGGGGAGCCAG[A/T]GACTGATTCGCTGCG | 221178 |
rs533207570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136628 | CCAAAGCTAATTTGA[A/T]GGGCTCAGCTTTGGG | 221178 |
rs533223699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178766 | TTTGTTTCTTTTTTT[A/T]AACAGCTTTATTGAG | 221178 |
rs533242067 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172459 | TGAAGGTTTTCTTTT[G/T]TGTTTTTTTCTAAAA | 221178 |
rs533249326 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160221 | GGGGGGTGGGGGCTG[G/T]CTGGTGGCTGAGGGA | 221178 |
rs533265266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071486 | TGTAATTTACAGATG[A/T]GAAGGCCAAGGCTTA | 221178 |
rs533273137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992379 | GATACTAAGTCCTGT[A/G]GTAAAGCCCAACATT | 221178 |
rs533274530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057852 | GGAGGTCAGGCTAAG[A/G]GAGACTCCAGATTCC | 221178 |
rs533279042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073729 | TTCTCAAGCCATCTA[A/T]TATCTTTTAAATAAA | 221178 |
rs533279148 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081035 | ACCTGCATGAATATC[A/C]ACAAGTTTTGTTCTA | 221178 |
rs533282061 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130881 | GTAATGTAAGGAGCC[G/T]GGAATCTCTGCAGGT | 221178 |
rs533293546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252089 | AGAAGTTTGCCCCTC[C/T]TGTGGTGTCCGTGTA | 221178 |
rs533308201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256813 | AGTTGGGATAATGAA[C/T]TTCAGTGGCACTTAT | 221178 |
rs533310693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051421 | CCTTTCAGCCACACC[A/G]GGTACAGCCTGCCAG | 221178 |
rs533329287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271284 | CTGATATTGTTACTA[A/G]TTTTGCTGCTGATAT | 221178 |
rs533336058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068437 | AGTGCTGTGCTGAAC[A/G]TACACGTGCTTGTGT | 221178 |
rs533337517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058426 | GACTGAGAAAATTGA[A/G]GCAAAATGGAAAAGC | 221178 |
rs533342361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263196 | TTATCTCTTGCTGCT[G/T]CTGCATTTTACTCAA | 221178 |
rs533357511 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24106670 | CCCTGGTTCTGGGGC[C/T]GACAGAGCTGGCTCT | 221178 |
rs533362595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992943 | TCTTCTGTTTACAAT[A/G]CAGCATGGGAATTTC | 221178 |
rs533367896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085939 | AGGCAGAGAAGCCAG[A/G]GAGGGTTTCCAGGGA | 221178 |
rs533375689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051891 | TCCTAGGAGTTCCCC[A/G]GCACCTGTTCCTCCT | 221178 |
rs533379324 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24215403 | ACAGGGAAAGGGCCT[C/T]TTCTGGGCCTCTGTC | 221178 |
rs533408110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045444 | AGTTTAAATTGCTGC[A/G]ACATGAAAACATCAA | 221178 |
rs533414210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270689 | GGAGCCAGCTGTCAG[C/T]TTCTGGGCAGGCTCT | 221178 |
rs533419150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095144 | CAACAGCCAAGAGGC[A/G]GAAACAACCCAAGTG | 221178 |
rs533471731 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080749 | AGACTCATCTTCTGT[C/G]CCCTATGGCATGTGG | 221178 |
rs533477128 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189789 | AATATATTTATAATA[C/T]AATAAATATATATTT | 221178 |
rs533486579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980201 | AAAAAAAAAGAAGAA[A/C]AGAAAAGTTGCCGCG | 221178 |
rs533499741 | in-del | -/T | 0.218151 | 0.247963 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104240 | TAAAGCTAGAATGGG[-/T]TTTTTTTTTTTGTTT | 221178 |
rs533511686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263923 | CCACAGAGTCCGAAG[C/G]AATTTAGAAATTATG | 221178 |
rs533512849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279770 | TTAGTTAGGAAGTTA[G/T]TGAAGCAAGGACATT | 221178 |
rs533532040 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303939 | AAAAACATTCAAACA[A/G]CTGTTTGCAATATAA | 221178 |
rs533534658 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24013693 | TTGTCCCTTACAGTC[-/T]TTTTTTTTTCCACTT | 221178 |
rs533583887 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113885 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA | 221178 |
rs533587928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017030 | GGCAGGAGGTAGTGA[A/G]GAGCGCCCGAAGTGT | 221178 |
rs533588348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284819 | CTTGATAAAGAATAC[C/G]CTCCCCTCCACTATC | 221178 |
rs533593874 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006306 | CAACTAACTCATCAG[C/T]AGGTAAACACACAGG | 221178 |
rs533602212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225364 | ACTGTAGCTGGCTTC[C/T]GCTGCAGGCACCAGC | 221178 |
rs533617127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991289 | TGAGATGTAAGTGTG[G/T]TTTGGGGCTGATTCA | 221178 |
rs533618568 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295251 | TCTGGCCAAGATTAA[-/T]TTTTTTTATCTTATA | 221178 |
rs533620210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240317 | CCTGGATGTCAATCT[C/T]AGTGTCGTGTTACTA | 221178 |
rs533626958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284430 | CTTTGGAAGGCCAAG[A/G]CAGGTGGATCATTAG | 221178 |
rs533631946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190533 | TTAACAGGAATTTGG[A/G]AGAAGTGGATTCCAC | 221178 |
rs533638790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086414 | CTTGGGTGACAGCTG[C/T]GGTCGAAGAAGACAC | 221178 |
rs533679138 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120864 | GGAGGGAAAAGTACA[C/G]TGAGTTCTATTCACA | 221178 |
rs533698879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195883 | ATTAGCTCAAGTGAT[A/G]TTTGGATTAATAGCA | 221178 |
rs533705218 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157386 | TCACTGCAAGCTCCG[C/T]CTCCCGGGTTCACGC | 221178 |
rs533707604 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136204 | ATAAACAATCATGTG[G/T]CTTATGCCTGTAATC | 221178 |
rs533708713 | snp | C/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978928 | GCTGCTCTTGAACTC[C/T]TGGCCTCACCTTGGC | 221178 |
rs533709907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289631 | AGAGAGTAAGTAACC[C/T]AAGACCACATACCAG | 221178 |
rs533711176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108449 | TCACTGTGGGTGCGT[G/T]GGCTTTGAGGAGTGC | 221178 |
rs533723620 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285220 | TTTTTAATTGTTAAC[A/G/T]ATCTCAAGATCATGC | 221178 |
rs533739614 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118212 | TCTGTGTTCCACCAC[A/C]TGACATTGCTCTGTG | 221178 |
rs533752612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294683 | GTGGATTATTTTGCC[A/G]GTCCTCATTTGTAAG | 221178 |
rs533753357 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24179213 | TTGTACTTTTTAGCT[C/G]TTAGGAATAATATGC | 221178 |
rs533756954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021442 | AGGCTACAGTGAGCT[A/C]TGATTGTACCACTCT | 221178 |
rs533769152 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234048 | TACCATTAAATAGGA[-/T]TTTCTCATTAAAAAT | 221178 |
rs533776322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072278 | AAAACTGTTGTCTCT[C/T]TTTAAGTACCGTACA | 221178 |
rs533780826 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24012203 | AATCTTTTCACCTGC[A/G]TCACAGCCAGACCCT | 221178 |
rs533782335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151864 | GCATAGTCTTTAACA[A/G]TACTAAGCAGTATAG | 221178 |
rs533787012 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23981317 | CTTTTTTAGAGCAGT[A/T]TTTTTGTAGCTACAA | 221178 |
rs533797046 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24267077 | AAGTCCTATCTCCTT[C/G]TTCTATCATGCCCCT | 221178 |
rs533803293 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181306 | TAAATTTATTGAAAC[G/T]TTTTTCATAATAAAT | 221178 |
rs533814286 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044849 | CTGAAAATATCCATC[A/T]CCTGGAGACAGTAAA | 221178 |
rs533818459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259380 | ACTTGCTTTCTTACT[C/G]TGGTAGATGTTTTCT | 221178 |
rs533828008 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278962 | TCCCTCCTTCCTTCC[C/T]TCCCTCCTTCCCTCC | 221178 |
rs533829332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248867 | CATTTTACTAATTCA[C/T]GATGGTGCTGATTTT | 221178 |
rs533830287 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194898 | AGTGAATCTTGTAAG[A/G]ATGAATTATGACTAA | 221178 |
rs533831800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204155 | GCATGTACTCACAGC[A/C]AGAGGCTAACCCGAA | 221178 |
rs533834046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039170 | CACAATGAATAAAAC[A/G]TTCATGGTGTATGAT | 221178 |
rs533834705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015666 | GTTTTTCCCTGCCAT[C/T]CCCTAGAAGGTCAGA | 221178 |
rs533836608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300619 | GCAGGTCCAGAACAG[A/G]GGCCAGGTGAAGGTG | 221178 |
rs533841897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072735 | CTTCTGTGCACCTAC[A/G]ATGCCCTTGGAGCCT | 221178 |
rs533842912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266326 | GTCTTGCTCTGTCAC[C/G]CAGGCTGGAGGGCAC | 221178 |
rs533851348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998239 | ATTCTCAACAGCACT[C/T]GGAATCATCAGTTTA | 221178 |
rs533858720 | in-del | -/TTAACAA | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177216 | CTGACTCAGTTACTT[-/TTAACAA]TTAAGAAATTTTTAA | 221178 |
rs533865915 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24289673 | TGTGAAGGCAGACCC[A/G]GGCATGCGGCTCCAG | 221178 |
rs533889627 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992012 | GTGGTTACTACAAGC[C/G]AAGCCCTCTGCTAAA | 221178 |
rs533897931 | in-del | -/ATC | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980966 | GGGAGTTCCTTAATT[-/ATC]ATTTAAAAAGTAAAG | 221178 |
rs533914782 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135469 | TTGGGAGACTGAGGC[A/G]GGCAGATCACGAGGT | 221178 |
rs533919747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248317 | TAAGGACCTGCTGTT[G/T]CCCAGGGAATGGCTG | 221178 |
rs533924032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130965 | TTACACAGGGGTGGA[G/T]CGGGGGACGCTTTCT | 221178 |
rs533933028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124679 | GTTTAGCAATTCTAT[A/G]TTGTATAGATACTGC | 221178 |
rs533933308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186873 | ATTCTCATGAAATTC[C/T]AATTGGTGAATTTAT | 221178 |
rs533958783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085514 | TGCCCTGTGGGGACA[A/G]CTGCAGGAACTGGGG | 221178 |
rs533963866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273081 | CAGAGCCAGCAGCCC[C/G]AGGACGAGCAGCTCC | 221178 |
rs533972419 | in-del | -/TTTATTTTTTATT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026573 | CTGTTTATTTATTTG[-/TTTATTTTTTATT]TTTATTTTTTGAGAC | 221178 |
rs533978038 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998558 | GTGTCTTTTGAAAAA[C/T]AGAAGTTTTAAATTT | 221178 |
rs533991591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120144 | TCCTCAGCCCTGTCT[C/G]CCTCTGTTCCTTCCT | 221178 |
rs534008848 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155497 | GTCCACACACACTCT[C/T]GGTGCCTAGATTCAT | 221178 |
rs534015257 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156356 | TTCCCCCCTCCAAAC[C/G]CAGGTGTGATGGGGG | 221178 |
rs534016241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215206 | TGGCATCATGTCACA[C/T]GACTGTCGTGCATGT | 221178 |
rs534018872 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079858 | TTACTTGACTCTCCC[A/G/T]TGAGGATGGGGATAC | 221178 |
rs534030590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208899 | CTTATACTGAAGATC[A/G]GATATTGGTGTTTTC | 221178 |
rs534042039 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24293132 | CTAAAGAGTTAGGAC[C/T]AAAGGAATTAGAAAA | 221178 |
rs534046636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272610 | GGACGCCATGTCAGG[G/T]AGGGCGGGTTTATGG | 221178 |
rs534053282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986196 | CCAGGGACCTAGTCA[C/T]TGTATAACCTCTTTC | 221178 |
rs534054251 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285017 | CTTTAGCTTTTTTTT[A/T]AGGAAATCATTCTGG | 221178 |
rs534064984 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253249 | AGAGCAGACAGTACT[A/G/T]TAAAGAAAAATAAAA | 221178 |
rs534070680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241413 | GCCATCTTGAACAGG[A/C]GCATTTGTGAGACGG | 221178 |
rs534076772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155984 | GTAATGTCCTCAGGG[C/T]CCACCTGTGTTGCAG | 221178 |
rs534079572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097721 | GAGGGAACCAACCGG[C/G]TACCTGGATCATGTA | 221178 |
rs534079588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221969 | AGGTGCACATCACCA[C/T]GCCTGGCTAATTTTT | 221178 |
rs534092665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283698 | AAGACACTGTTGGGA[C/T]GTACTGGTTTTAGTA | 221178 |
rs534136111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161538 | GTTTGGTCCCATTCT[C/G]TGCAGGAGGTGGGGG | 221178 |
rs534149923 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24149705 | GGGAAAGCTCCCACC[C/T]ATGTGGGGAAGAACC | 221178 |
rs534153162 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133475 | GGAAGGACAGACAGG[A/G]TCGGCCCTGGAACTA | 221178 |
rs534162453 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251975 | CTTGGGCCAGGGCGC[A/G/T]TTTGTCTGGGAGTGA | 221178 |
rs534168672 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24025363 | ATAATAATAATACAT[G/T]TGTATGTACATTCTT | 221178 |
rs534191336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247285 | TTGAGCAGAGGTGAC[A/G]TGGCATTGCAGGAAA | 221178 |
rs534191473 | in-del | -/AT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24239707 | TAAAAAAAAAAAAAA[-/AT]AAAAAAAAAAAATAG | 221178 |
rs534196618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147248 | GGCAGAACAGGATGC[A/G]GAGAAGGTGGAAAGG | 221178 |
rs534201213 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305713 | GGGCCAAGAAAAGAA[A/G]AGATGACATAACATT | 221178 |
rs534201350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010052 | TGAGACATCAATCAA[A/T]TACATGTAAGATGTA | 221178 |
rs534201814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141793 | TATCATTAAGTGAAC[A/G]TTGTTATTTTTTCTA | 221178 |
rs534205459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228271 | GGCACCTGCCACCAT[G/T]CCCGGCTCATGTTTT | 221178 |
rs534207678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092088 | TGGTGAATTTGCAGT[A/G]TTTTGAAAAACTTGT | 221178 |
rs534211012 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157521 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCG | 221178 |
rs534231645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103766 | GATAAGAGGGTAGTG[A/G]GATAAGGTTTCCCTG | 221178 |
rs534238787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010718 | TTCCTCCCCACTCCT[C/G]CCTCCCTCCTGCTCC | 221178 |
rs534240603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004071 | GTGGGCACTCCTGGG[A/C]TTTGGTCTGTCCTCA | 221178 |
rs534247538 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258671 | GACCTCCTCTCCGCT[-/A]AAAAAAAAAGAGAGA | 221178 |
rs534252653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069427 | GCTCTTGGCTTCACT[C/G]TTTTGGTATGTAAAA | 221178 |
rs534252888 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125201 | ACTGGCTCTGGAATC[A/G]GTGCTTAGTGGCTCA | 221178 |
rs534264559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252508 | CAAAAACGTATACCA[C/T]GTTTGTAACAATATG | 221178 |
rs534266388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063452 | TGTAAGCGCCTCTGG[A/G]CTCTGACTGCCATCC | 221178 |
rs534277853 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189892 | TATATCATAATATAT[-/A]ATTATATAATTATAT | 221178 |
rs534292936 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297277 | ACTCTTGGCCTCAAC[A/G]ATCCTCCCACCTTGG | 221178 |
rs534304752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197775 | TTTTAAAAAATATGT[A/T]TAAGGATTAGTGAGG | 221178 |
rs534307713 | snp | A/C | 6.84463e-05 | 0.00584965 | intron-variant, missense | SPATA13 | GRCh38.p7 | 13:24278747 | AAAAACAAAGAAAGA[A/C]ACTTGACCAAGGACT | 221178 |
rs534311876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133980 | GGGGCTGGGTCGAGC[C/T]CCTGGGGGAAGGCTC | 221178 |
rs534313759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053655 | CTGAGCTGTCTAAGA[C/T]ACCTGGGGCTCCATC | 221178 |
rs534316535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192021 | CGGCAAAGTGAGATG[A/G]AGTCCTGCTAACAAG | 221178 |
rs534318027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262586 | AAAAAGTGAGAGTGT[A/G]ATCCCAATCCTTGGG | 221178 |
rs534330985 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112643 | ACAAACAGCTCATTA[C/T]AGCTGTTTGTTTGTT | 221178 |
rs534331837 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24038933 | CAGAGAAACCTGCTC[A/G]TCCCAGGCAATGGGC | 221178 |
rs534347083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080396 | TGAGAACAAAAGCTT[C/T]GGCGGCTTGGGCCCA | 221178 |
rs534347301 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989058 | ATTTACTGAAATGGT[A/T]CATATGCTGAAGAAA | 221178 |
rs534348526 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23983445 | CATTCTGAGGTACTG[A/G]AGTCAGGACTTCATC | 221178 |
rs534352519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270067 | AGGTCACTACTTTGC[G/T]TATATATTACCTCAT | 221178 |
rs534365709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277536 | GAAGACTGGCTGAGG[A/G]ATTTTTCTAGCTAGA | 221178 |
rs534373141 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183842 | AGGCTTAGAGGCACT[C/G]ACTCTCATCCTGGTT | 221178 |
rs534376334 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268754 | ACAGAGCAAGACTCC[A/G]TCTCAAAATGAAATA | 221178 |
rs534380612 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090924 | CCTCCTCTCTCGGAT[A/T]TTTGTTGCTGATGAT | 221178 |
rs534399041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088664 | CAAAGCTCAGAATCA[C/T]TGCCTTCCAGAAGGT | 221178 |
rs534399987 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24097765 | CCCAACATAGCCAAA[A/G]GTATGCACCGGAAAG | 221178 |
rs534401960 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153850 | AATTCATCCCTTGGG[G/T]TTGGAATCCTAGCCC | 221178 |
rs534418415 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24001445 | GGGTGGGGTTCGGTG[A/G]GGCTGGAAGTTTGAG | 221178 |
rs534462584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231176 | TTCAGTGATTTTTAT[A/G]TGTTTATGGAGCTCT | 221178 |
rs534476047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275806 | GGATGTGATGGCACG[C/T]ACCTGTAATCTCAGC | 221178 |
rs534496185 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24055900 | GACCACGCTACATTA[C/G]ACAAATGGCGTTGGC | 221178 |
rs534504775 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110219 | AGCTGTGTTCTGCTC[A/G]CTGAGCCGGCTCTCC | 221178 |
rs534506796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201402 | ACAATTGATGGGTCA[A/G]TATTGATTTACTATT | 221178 |
rs534512180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237334 | CACCACTGCACTCCA[A/G]TGCTGGCGGCAGAGT | 221178 |
rs534513499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076930 | AGCAGATCGGCTCTT[C/T]AACCTCGCCTTATTC | 221178 |
rs534544774 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24236674 | AATCATTAGGGAAAT[A/G]CAAATTAAAACCATG | 221178 |
rs534550374 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218896 | CTGTTCTATATTCCT[A/G]AATTTCAAATTTAAG | 221178 |
rs534551041 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041297 | TTTTAACAAAGGACG[C/T]TTCAACCTGAATTTT | 221178 |
rs534554992 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057263 | ACAGTCCCCGGAGTG[C/T]GATGTTGGGAAATGG | 221178 |
rs534570707 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303529 | ACACTGGCTTTGTCC[C/T]GGAGTCGGATTCCCT | 221178 |
rs534571603 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071081 | GATGAATGCACTCAT[G/T]GTTCAGGGAGGACTT | 221178 |
rs534572782 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304285 | GATAATCATCTCCTT[G/T]TCTTTGTCTATGTTG | 221178 |
rs534583480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157949 | TAACTGTACCTCAAG[A/G]ATTGTCTTGAGGATT | 221178 |
rs534591126 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065005 | CAGGAGCCAGGATAA[-/T]TGAAATGCAACGTGA | 221178 |
rs534598931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184283 | ATGTTTGGTTTTGCC[C/G]TGAACCCAAGGAGCC | 221178 |
rs534608669 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303117 | CAAGTGCCTGCTGCA[A/G]GTCCAAACACAGCAT | 221178 |
rs534630252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243906 | TTAATTTTCTTCTGA[A/G]TTACCTTGCTGTATG | 221178 |
rs534630727 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24127673 | TTTTCTCACAAAGCA[C/T]TGGTAAATCTCCATA | 221178 |
rs534668517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122062 | AGGAAAGAAAGAGAT[A/G]ACTCAATTCATCCCT | 221178 |
rs534680308 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24231356 | GGAATCCTGTAATAC[A/G]TGGTCTTTTGTGACT | 221178 |
rs534682822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106874 | TTCTAGATAAAGCAG[A/G]TCGAGTGAGTTTCAG | 221178 |
rs534682925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204970 | CATGTATGACAAACC[C/T]ACAGCCAATATCATA | 221178 |
rs534684007 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23983827 | GAGCTGCAGAGTGAT[A/G]GGAGTCATATTCGCT | 221178 |
rs534698098 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283047 | GATCTTTGCAGTCTT[C/G]TCTTTCATGAGATGT | 221178 |
rs534702717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013246 | ACTTCTCCTCAGCTC[A/G]GCTCCCGCTCTGTAA | 221178 |
rs534709106 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042636 | GGTGTATTCATTACC[-/A]GGGGGTAAACCTTAC | 221178 |
rs534723018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195378 | ATTTGGTTCGTTTCC[C/T]CCTTTGACCATTATG | 221178 |
rs534742511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006921 | CTGGAAGGAGGATGC[G/T]GTGGCATTGCCTGGG | 221178 |
rs534743468 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024092 | AGAGGCTCTGAGTCA[C/T]GTGCTGCGGAGGTCA | 221178 |
rs534756063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001404 | CTTCTGAGAAGGAGG[G/T]TGTGAGAGAGGTGAG | 221178 |
rs534772588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281163 | GTAAGAAAGCTAGGG[C/T]CCAGAAGGCAAGACC | 221178 |
rs534778536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060945 | TCCAGAGGCTAAGAC[C/T]GGAGAATCACTTGAA | 221178 |
rs534787196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117056 | CTATTATTTAAGCCA[C/T]GCAGTCTATGGAATT | 221178 |
rs534801895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295814 | CCTCTACACCATCCT[A/G]TGAAGTAAGCACTAT | 221178 |
rs534807529 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985381 | CCCCAGGAACGGCTG[A/G]TGTGGGGGCTCAGTG | 221178 |
rs534812746 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207108 | TATCCTCAGCAAACT[A/G]AAGCAGGAATAGAAA | 221178 |
rs534831285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149630 | CTGTGGTGTAGTGCA[G/T]CGTCCTGAATTTGGA | 221178 |
rs534833315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158474 | AAAGCAAGAATAAGC[A/G]TCGGCTGGTGATGTA | 221178 |
rs534842233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216364 | TGAATCCCTATTGGG[A/G]AAACACCATTCTCAC | 221178 |
rs534848376 | snp | G/T | 0.000563274 | 0.0167726 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223347 | TCAAAGGGAGAGGCT[G/T]CGGAGCATGGCCTGG | 221178 |
rs534854183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117705 | AAACCCCAAACTCAT[C/T]CCTTTACTCTGATGT | 221178 |
rs534854199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112068 | AAGCAGCATTTTTAT[A/T]CAGTTGATGCATCTT | 221178 |
rs534858550 | in-del | -/T | 0.00639099 | 0.0561663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168849 | TTTTAATTTTAAAAA[-/T]TTTGAAGTTAAATAA | 221178 |
rs534859189 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143602 | TCTTTTTTTCCCAGG[A/C]TTTCCGACTCTGCTG | 221178 |
rs534893529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144176 | TCCCAAAGATGCTAA[A/G]CCCCTGCCTCTTGGG | 221178 |
rs534898043 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031720 | TTTATAATCTTGGAC[C/T]TTCTCTCTCCCTTAA | 221178 |
rs534898791 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129111 | ATCCTATACTTTAAA[G/T]AAGTGGCTTCTGCAG | 221178 |
rs534898821 | in-del | -/TT | 0.318174 | 0.240525 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285681 | GCCACCACATCTGGC[-/TT]TTTTTTTTTTTTTTT | 221178 |
rs534904031 | snp | C/T | 0.00116302 | 0.0240864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222813 | CTGCTTTGTCTTTCA[C/T]TGCAGCCCGTGGCCA | 221178 |
rs534911978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089825 | CTCGAGATTGGAAGT[C/T]CAAGATCAGAGCACC | 221178 |
rs534917553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112415 | ACGTGTTTTATCTCC[A/G]ACCAGAACTTGAGCT | 221178 |
rs534926694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106426 | CTCAACTTTTCCTTG[G/T]ATATGAAAATGGAAA | 221178 |
rs534930402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205816 | TTTGACAAACCTGAC[C/G]AAAAACAAGCAATGG | 221178 |
rs534942059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008445 | GCTCTTAGTGCCTTC[A/G]TCATGGGCCACCATG | 221178 |
rs534954840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171079 | TACAGAAGGAAGACA[A/G]TTTGCATGGAATTTT | 221178 |
rs534964177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250165 | AGACTCCTGAAAGAA[A/G]TAATTGTTGAAAAAG | 221178 |
rs534966133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996903 | TCCCTTATAAGGATC[C/T]TTGTGCTCACAGTGG | 221178 |
rs534971269 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24009469 | CTACAGCCTAGTTTT[A/T]TACATTTTAGGGAGA | 221178 |
rs534985890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291295 | CTTGAGGTTGACGTA[C/T]AGCAGCTCGGCTCAG | 221178 |
rs534987137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229933 | GTAAAAGCAAAATGC[C/T]ATGGGTTTCAGAGGA | 221178 |
rs535001908 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24069822 | TGTACATAATCTAAG[A/T]CCAAATGGCACTGAC | 221178 |
rs535002552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118653 | TTCCTGGTGATGCTG[A/G]TGCAGTAGCTTCAGG | 221178 |
rs535010314 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24301425 | ACAAATATCTTTAAG[G/T]CAGAAAAACCCATGT | 221178 |
rs535017210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170664 | AGATGAAGATAATGG[A/G]TATCTGTGCCAATCA | 221178 |
rs535018665 | snp | A/G | | | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223862 | ACGCTGGAGGAGCCC[A/G]ATAAGGGCCAAGGAC | 221178 |
rs535022573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296253 | CATCAGTGAAGAATC[C/T]AGGGCACGGAATTGC | 221178 |
rs535025270 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026391 | GAGGTGTGAAGCAAA[G/T]TAGAGATCCTCTCTT | 221178 |
rs535046189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208809 | TCAGAAAAGTTTCAG[C/T]TTCTTCAGAAATTAC | 221178 |
rs535052905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078612 | CAGGCCTGGGCAGTT[G/T]TTATTTGTTGTTACT | 221178 |
rs535062848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288792 | TGGATCCTAAATCCA[A/G]CCGCATGAGCCTTTT | 221178 |
rs535065574 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128348 | CTGGAACTTGCCTAA[A/C]CTGCTCTGCAAAGGT | 221178 |
rs535075810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048144 | CCCAGAAATACCCTC[A/G]ACACACCCCAGAAAT | 221178 |
rs535077808 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24232177 | CCTGGAAGCCTGAGG[A/G]CAAGGTGATGGGGTG | 221178 |
rs535077909 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258354 | TACCATGAGAATGAA[C/G]AGTTCATCTCAAAAA | 221178 |
rs535084265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140088 | AAAAAAAAAAAAAAG[C/T]CTGTAACATGCAAAG | 221178 |
rs535084300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176171 | ATCCATTTTTTGTTT[C/T]ATTTCTTGAGAAATT | 221178 |
rs535084579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134465 | ACATAGAGGTCGTAT[G/T]GATGCCGAGAGCAGC | 221178 |
rs535108580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048757 | CTCTCATAAAGTGTC[C/T]CTAAAGCAAAGGAGA | 221178 |
rs535113435 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278910 | TCCTTCCTTCCTTCC[C/T]TCCTTCCTTCCTTCC | 221178 |
rs535118111 | snp | C/T | | | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978500 | TCATTCTTTTACTTT[C/T]GACTCATTTGTACTT | 221178 |
rs535123625 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229262 | CTAAATATGCCATGG[-/A]AAAAACTCTTAAATG | 221178 |
rs535145742 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067027 | CCATCCTCAGTATAC[C/T]CAGTTCAGAGCTAAA | 221178 |
rs535147949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134921 | TGAAGTCATTAAGGC[A/G]GGCTCCAATCCAACA | 221178 |
rs535166493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213936 | TTGAAGGAATCTGAA[A/G]GCATGTATGATCCAT | 221178 |
rs535191318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042997 | GAGAATGAACCCTTT[C/T]GCAATGTGTGTCTTA | 221178 |
rs535199019 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038209 | TGAGCCACCGCGCCC[A/C/G]GCCAACTAGGCTAGA | 221178 |
rs535204023 | in-del | -/TAAATCAAAGACAATTTTGTTT | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995269 | CTAGAAAGACAAAGG[-/TAAATCAAAGACAATTTTGTTT]TGTGATCTTTGAACA | 221178 |
rs535204884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117893 | TTCAGCTTCGAGAAT[A/G]TAATTGGGTTGTTTA | 221178 |
rs535205974 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24234097 | AATCATACCCCTATA[A/C]CTGCACAAGAGACTA | 221178 |
rs535219611 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150109 | CAATGCTGAGATTCT[C/T]AGGTGGACTGATGGG | 221178 |
rs535223828 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24179346 | GAAATTTTGGAAGAA[C/T]TGCCAGACTATTTCT | 221178 |
rs535224011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213371 | TCCTGGGTTCAAGCA[A/G]TTCTTTTGCCTCAGC | 221178 |
rs535224029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220655 | GCTCCTCTGGCCCCC[A/T]AATTCCTCCATTAGA | 221178 |
rs535225391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268228 | CCAAAAGGTAGATAC[A/G]ATATACAGTGGTTTT | 221178 |
rs535243274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299377 | GTCTGTGAACTGGCA[C/T]GTGTGGGATAAAACT | 221178 |
rs535259071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274739 | CAAGAGGTTTTCTCA[A/G]ATACATGATTTTAGC | 221178 |
rs535264737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049643 | TATAGGGAGTCTGTA[A/G]TATACATGCAATGAT | 221178 |
rs535275114 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304908 | ATGTGTTTATAGAAC[A/T]GACCTTTTTACTAAC | 221178 |
rs535277291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150696 | GCAGGCCACAGCAGG[C/T]TGGGGATTCAGGCAG | 221178 |
rs535277355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059207 | CGATCTCCTGACCTC[A/G]TAATCCACCCCCCTC | 221178 |
rs535281367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186189 | CTACCAGTGAGGAAA[C/T]GGGAATGTTACGGTT | 221178 |
rs535300062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071600 | GGTCTGACTCAGCCC[C/T]CTGTAGTATGGAGCT | 221178 |
rs535307644 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022944 | GAATCTTCTTTTTTT[-/A]TTATTATTATTATAC | 221178 |
rs535330260 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032601 | CCCTGTCGTTTCTGC[A/G]GTAATGGAGAGTATA | 221178 |
rs535338216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066519 | CACCATTTTACCACC[C/T]TGGGACAAACCTGTC | 221178 |
rs535358163 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304313 | TTGTACATTTTCATG[A/G]TATAACTTTTAACTA | 221178 |
rs535374762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191505 | TACATTGCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 221178 |
rs535375544 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084478 | CCCTGACTCACTTCA[C/G]CCCTCTTAGCACCAC | 221178 |
rs535382181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021396 | TACTTTGGAAGCTGA[A/G]TCAGGAGGATCACTT | 221178 |
rs535388678 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984467 | AATAGAAACCGTGTG[C/T]ATTGTTCTAGGAATC | 221178 |
rs535393718 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202091 | AAATAAATAAATAAA[A/T]AAATAAATAAATAAA | 221178 |
rs535396250 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283188 | TGGGGAGGATCCCTT[C/T]CTCTTTAAAATCCTG | 221178 |
rs535398205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088697 | ATAGTAGAAACTCAG[C/T]GGCACTCGGGCCCTG | 221178 |
rs535399787 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265512 | ACTCTCCCATCCCAA[C/T]TTTAGAAAGTGCAGC | 221178 |
rs535412868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122394 | AATGATTGTGGAATA[G/T]CCTTCCAGAGCAGTC | 221178 |
rs535416254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140227 | AATGCAAGCCTAGTC[A/G]TTTAGGTTAAAGTTC | 221178 |
rs535425570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054695 | GCGCACCGTTAATTT[A/G]TGATGGTTCTTAACC | 221178 |
rs535438719 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992374 | AGGGTGATACTAAGT[A/C/T]CTGTAGTAAAGCCCA | 221178 |
rs535446388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168104 | CTTCATGAGCCTTCT[A/G]TGAACCCTGCTGAGA | 221178 |
rs535446791 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24067458 | AAAGAACTACTTTTC[C/T]ATCAAATACCAAGCC | 221178 |
rs535446909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013836 | ATACAGTCAATAGCC[A/G]TTTGACCCATGAGAA | 221178 |
rs535461894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208301 | GCCAAAAAGGCTGAT[A/G]ATAACCTGTGTTCCA | 221178 |
rs535480317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117217 | AATAACAAATCTACA[C/T]ACAGATTTAGTAATC | 221178 |
rs535483327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232425 | CACCCTCACAAACGC[A/T]CCCAGAAATAATGCT | 221178 |
rs535484394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007536 | AACTTGGCCCACTGC[A/G]ACCTCTGCTTCCCAG | 221178 |
rs535485935 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978477 | ATGTTTCCATGGTAT[A/G]CGTTTTTTCATTCTT | 221178 |
rs535495259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001810 | GGTGAGGGAGCAGGG[A/G]TGAGGACTGAGCAGG | 221178 |
rs535497920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096274 | GTTATGGTTAGTGCT[G/T]TAAAGAAAAAAGAGT | 221178 |
rs535502380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282079 | CTATTTACAGAATTG[A/G]TTGCTTGTGACAGCA | 221178 |
rs535506400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196387 | ATACCTATTTTTAGT[A/G]TGTAATAAAGCCTTA | 221178 |
rs535510018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276992 | AGCAATTCGTAATTC[A/G]ATTGAACAATGTCTA | 221178 |
rs535512814 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24090572 | CAGACTACTGAGCAT[C/G]GTTCTTTCCATTCTG | 221178 |
rs535522737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061904 | AAAAAAAAAAAAGAA[A/C]AAAACTGAGGCTCAG | 221178 |
rs535528935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200942 | TGTGTCTGATTACGT[C/T]CTTGTTCTTTTTTTT | 221178 |
rs535533589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089896 | AAGATGATGTCCTGC[A/C]GCTCTGTCCTCTGGA | 221178 |
rs535542912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055865 | GTCCAATCCACCACC[G/T]CACGGGTCCAGAATA | 221178 |
rs535556188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258042 | CAAAACTAGCCTAAC[C/T]AACATGGTGAAACCT | 221178 |
rs535571292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281678 | CAGAGGGGGAAGCAA[A/C]TGGAAAGCCAGAGCC | 221178 |
rs535572512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173171 | CACCCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 221178 |
rs535574753 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24217218 | GGCAACATAGCAAGA[G/T]TGAGTCTCTTAAAAC | 221178 |
rs535577085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014753 | GAAACAAATCCTGAT[G/T]TCAATTGTGAATTAA | 221178 |
rs535579026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049676 | CAACCTCAGGCTACT[A/G]AAAACACGAAACTGA | 221178 |
rs535625591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996965 | CTTTTCCCAACTTAT[A/C]AGCAGGAGAATGTGG | 221178 |
rs535645951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001548 | GCCGGGCTGGCTGCC[A/G]TGTCTGTTAGGGTCA | 221178 |
rs535651884 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24192747 | GCAGAGAGAAGATTT[G/T]TTGTGGAAGGGGTGC | 221178 |
rs535658908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172492 | TTCGTGGTTTTTCAT[C/T]TTACAGTTAAGTCCA | 221178 |
rs535674714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084675 | GGGCACACCATGGCC[A/T]TTTGAGTAGTTAGCA | 221178 |
rs535677951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106977 | TTGACTGATAGGATT[C/G]TAGTGCATTTGCTCT | 221178 |
rs535678268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113104 | TCTTTCCTAAAGTTT[C/T]CTGAAATGCTACTTG | 221178 |
rs535679906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038328 | AGCAAATCCTTCCTC[A/G]ATTGTGCCAGGGGGC | 221178 |
rs535682490 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264364 | CCAAGAGCCAGTAGC[A/C]CTCTGTACGTATTCC | 221178 |
rs535692986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185697 | TCAATTCCTGGATTT[A/C]ACTTAGAACACATAC | 221178 |
rs535695068 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075321 | TTATATCTCCAGAGC[C/T]TGGATCTCGGTTTGG | 221178 |
rs535696336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206707 | GACCAGCCTGGCTAA[C/T]GTGGTAAAACCCTGT | 221178 |
rs535703862 | in-del | -/TTTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24014902 | TTTTTTTTTTTTTTT[-/TTTTTTT]GAGACAGAGTCTCGC | 221178 |
rs535713548 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072115 | ACAAAATTGAACACA[A/C]AAGTACATGAGAGAA | 221178 |
rs535713978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178327 | ATTAGCAGAAATGTA[C/T]TGAACTGCATTATGA | 221178 |
rs535717102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171773 | AAAGTTTTGGTGCAT[A/G]GATGAGTTTCCTCAG | 221178 |
rs535732983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101513 | AACACATAAAACTTA[C/T]CACCTTAACCATTTT | 221178 |
rs535733342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085382 | TCCGCCCACCTCAGC[C/T]TCCAAAAGTGCTGGG | 221178 |
rs535746258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991069 | GAGGAGAAACAGACA[C/T]CTGCTTAACTGTCCT | 221178 |
rs535747535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251002 | ATTACATAAGCAGGA[A/T]ATGCATGTAATAAAC | 221178 |
rs535782500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114003 | TGATCTTTCATACAG[A/G]TTACTTGAGGGATGA | 221178 |
rs535783621 | in-del | -/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128750 | TAAAAAAAAAAAAAA[-/AA]CTGCTTACTTCCCTT | 221178 |
rs535785048 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169815 | GGTGGCTCAGTGAGT[-/C]CCCACTCTCCTCTCC | 221178 |
rs535785194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003942 | GCCACACTCCCCCTC[C/T]TCCTGCAGCATTGTT | 221178 |
rs535792904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173170 | GCACCCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 221178 |
rs535800977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154892 | GACGGAGTTTTGCTC[C/T]TGTTGCCCAGGCTGG | 221178 |
rs535825406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063826 | GTCCTGAATTTGTGT[C/T]GTTTCCTGCCTCACT | 221178 |
rs535830305 | in-del | -/TAAT | 0.00479135 | 0.0487105 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141336 | AATTAACCCTACAGA[-/TAAT]TAATTAATTAACATA | 221178 |
rs535833782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985070 | TAAGGAACAGAATAA[C/G]CAAACACAGATGTGT | 221178 |
rs535834973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987750 | CTCTTTTTATTTTAC[A/T]CAATTGGAATTCCCA | 221178 |
rs535845005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016937 | GTTTTAGTTACTGAA[C/T]GACAGTGGATGGTGG | 221178 |
rs535850778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020980 | CAGGAGGCGGTGGTT[G/T]CACAGGGCCTAGATC | 221178 |
rs535854841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240111 | GGAGCTCAAGACCAG[C/G]CTGGCCAACATGGCA | 221178 |
rs535865390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154414 | TACTGTTAAGGAAGT[C/G]AGACACAAAAGTATA | 221178 |
rs535869384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981502 | TCACAGTTTCGGGAG[C/T]CGGAAATGCTAGGAA | 221178 |
rs535893175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193856 | AAGTGGTCACAATGA[A/G]GAAGATGGATGTGGA | 221178 |
rs535916496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239138 | TGTTCCTCATGTATC[C/T]GAGACTAAGTAAAAC | 221178 |
rs535923380 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159868 | ATCATCTAAAAAACT[A/G]CACTGGTAGAAAGCA | 221178 |
rs535939982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097008 | GGGGACAAAAGAGGA[G/T]ACAAGGAGCCTAGTT | 221178 |
rs535948590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056603 | CCCACAGAGCCCAGC[A/G]CAGTGTCTAGCACAT | 221178 |
rs535952299 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021331 | GCATAAAGATGATTA[A/G]GAGAATATCAGGCAT | 221178 |
rs535959930 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099422 | AATGTTAGTTCCTCA[A/G]TCTCAGTGGCCACAT | 221178 |
rs535971451 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147397 | ACCATCATGTGAAAG[C/T]TGTGCTGATTCATAG | 221178 |
rs535974322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123170 | ATGAAGAAGAGCCTG[C/T]ATTACAGGTCTGATG | 221178 |
rs535982525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246172 | GTGAGCAGGTGGACA[G/T]TTCCCTGCCTGTGGT | 221178 |
rs535986023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166844 | CATTAATCTCCTTCA[C/T]GAGAGGGGAGCCCTC | 221178 |
rs535995752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284869 | GATCTAAGAAGCGGA[C/T]ATTATGGTTATTATC | 221178 |
rs536000776 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147713 | CCATCCATCTCCAGA[G/T]CTGAAACTGAAACCC | 221178 |
rs536003720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086788 | ATTCCAGGAGGGAGA[A/G]GGGTGGGAGCTGTTG | 221178 |
rs536018820 | in-del | -/GGAGCTTACATTCTG | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279078 | AATTACTGCCTTTCT[-/GGAGCTTACATTCTG]GATAGTGAACAGAAT | 221178 |
rs536049409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052936 | CAGGGATATTTTGGG[A/C]CTGGGAACCTTGGCT | 221178 |
rs536049595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043820 | TTTCTATTAAATACC[C/T]TTCCTGACTCTATTG | 221178 |
rs536071827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012038 | TACTGAGAAGATGAA[A/G]GCAGTGGTTTCTTGC | 221178 |
rs536086570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044324 | TGCAATCTCCACCTC[C/T]TGGGTTCAAGCGATT | 221178 |
rs536111921 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105998 | GAAATACGTTTCTGT[C/T]GTTTAAGCTACCCAA | 221178 |
rs536115510 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254401 | AGTCACTGCTTCAGA[C/G]CTTGCGTCCCATCCA | 221178 |
rs536120027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256949 | CTGCTAGAAGATTTT[C/T]CTGGGGAATTATCTT | 221178 |
rs536129208 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287597 | TGTCACTATCTGCAA[-/C]CCCGCTGCATCTAAT | 221178 |
rs536139342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295058 | CTACTTTATACCCCA[C/T]TCCCATAAGAAATAA | 221178 |
rs536145796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211887 | ACCCCAACATCCGTC[C/G]TTTCTCTGGCATTAG | 221178 |
rs536152213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259991 | TACTTCCTTGATTTC[A/G]ATCCATTTAACAAAT | 221178 |
rs536166023 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24021868 | AGGCGCCCGCCACCA[C/T]GCCTGACTAATTTTT | 221178 |
rs536167236 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278953 | TTCCTTCCTTCCCTC[C/T]TTCCTTCCTTCCCTC | 221178 |
rs536172573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044913 | TGGGGGTAGGCAGAG[A/T]GAAGAGAGGTTGGTC | 221178 |
rs536174704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107656 | ACAGCCCAATGACAG[C/T]GCCTACGTCAGCTTT | 221178 |
rs536175127 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174734 | GGTGTGTGTCACCAC[A/G]CCTGGCTAATATTTG | 221178 |
rs536178517 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24280756 | GTTGTTTCCCTTGGA[A/G]TCTAAAACACACTCA | 221178 |
rs536179140 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000814 | CAGAGGTTTGAATTC[A/G/T]GGAGAACCCTGGGTG | 221178 |
rs536190112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152541 | CTTGCACAGCGGGTG[C/T]TCTATGCCAGTGAGG | 221178 |
rs536192206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079699 | TTTTTTATCTAAAAT[C/T]TCCCTTGGCACAGTG | 221178 |
rs536196955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082271 | CACGTAAGTGTTCTG[A/T]GGCAGGGGCAGGCTT | 221178 |
rs536216700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104208 | TGGGGTGAACCGTTT[A/G]GATTTGTTGAACAAT | 221178 |
rs536222855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259426 | TGGTCTGAATAAAGA[A/G]AAAACAAAAACGTAC | 221178 |
rs536236460 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24056306 | TTAGGACCCATTTAG[A/T]GATGCTTTGGAAGTT | 221178 |
rs536241038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137758 | TTCAACAGAGTGAGA[A/C]TGTCTCTCCAAAAAA | 221178 |
rs536247647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181436 | ACAGCTGTACAAATA[A/T]AATTTCTTTATAGCC | 221178 |
rs536257764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076299 | AGTGGTTTATCTTTG[C/T]GTGCCAGGTTATAGC | 221178 |
rs536264324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023409 | TACTTTGCTTTTTAT[C/T]TTCTAATTTCAATAG | 221178 |
rs536277366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098851 | AGAATTGCTTGAGCC[C/T]AGGAGGTGGAGGTTG | 221178 |
rs536280472 | in-del | -/TT | 0.0414363 | 0.137845 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142110 | ATTTGTAGGGAAAGG[-/TT]TTTTTTTTTTTTAGC | 221178 |
rs536285393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030180 | AACCAACACTGACAC[A/G]TCATTGTCACCCAGA | 221178 |
rs536308388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243732 | TTGCAGTCCTCTGTG[A/G]CATCAACTGCCAAGG | 221178 |
rs536311169 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250171 | CTGAAAGAAGTAATT[G/T]TTGAAAAAGACAGTA | 221178 |
rs536314708 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266438 | TCAAGGCATGTGTCA[A/C]CAAGCTGGGCTAATT | 221178 |
rs536322822 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215767 | CAGCTCCAGATTTGG[C/G]CCAGTCTGCCTCTGC | 221178 |
rs536335267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031086 | CATTCAAAGTAGCAA[A/T]TGGTTTTAAAGCTTA | 221178 |
rs536339139 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24088223 | CTCCCTAGGCAGCAC[C/T]GGATGCCCACAGTGT | 221178 |
rs536356352 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052173 | ACGGTTCTCAAGAAT[C/G/T]GCAGGCCTCGGGCAC | 221178 |
rs536374856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132560 | CTGTGTTGAAACTAA[A/C]ATTATTTAAAAGTAT | 221178 |
rs536385997 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235105 | TGATTGAAATTATTT[C/T]CTTTGGTCAAACATT | 221178 |
rs536417784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106143 | GACTCTTGCAACCCT[C/T]CTGCCCCAGCCTCCC | 221178 |
rs536434715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126576 | GACTCCCAGGGCGCA[A/G]GACAGAGACAGGTTC | 221178 |
rs536446622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139553 | GGTGCTGCAGAAAGC[C/T]GTGTCCTCCAAATTT | 221178 |
rs536447922 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24251626 | TTTCACGTCTGTGAG[C/T]GGCTTCGAGGTGAGA | 221178 |
rs536448066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133462 | GTCAGTGGGCACAGG[A/C]AGGACAGACAGGGTC | 221178 |
rs536454692 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068977 | TGTTCACTCTGTTGA[C/T]AGTTTATTTTTCTGT | 221178 |
rs536471834 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24297319 | GCTAGGACTACAGCT[A/G]TGGTAGAATTGGAAG | 221178 |
rs536475856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203702 | TTTCTCTTTTTTGTT[A/G]GTAGGTATTTGGGAG | 221178 |
rs536477065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100773 | GAGCTCCTCACTCCC[A/G]TGCTGCCTGTAACTT | 221178 |
rs536478279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209905 | GTGAGGGTCTCCTTT[C/T]TTGCACATCCTTACC | 221178 |
rs536480216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046877 | CAGAGATAAAATCAG[G/T]TCACTGAGACAGCGG | 221178 |
rs536491871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121546 | ATGAATGAAAATGAT[C/G]AAGATTGAATAAAGC | 221178 |
rs536497618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248417 | TGAACATGTCTGCTC[A/G]ATTCCCAGCATCATG | 221178 |
rs536513982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175146 | CTAGGGCGGAGTTCT[A/G]TAGCTCTCTAATCCT | 221178 |
rs536516282 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125930 | TTTCAAATGTTCCCT[A/G]TTGCCTATGCTTTTC | 221178 |
rs536522167 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24227838 | GCCTTCCAAAGTGCT[A/G]GGATTATAGGTGTGA | 221178 |
rs536523894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162341 | AGCCACAGCCTGCCC[C/T]GCCTGGAGGGCACAC | 221178 |
rs536534478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081732 | AAATTAAAAATTGCA[C/T]ACTATGTTTTAAAGA | 221178 |
rs536543209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209534 | ATTTGTCTCTCTGTG[C/T]CTGGCTCATTTCACT | 221178 |
rs536544665 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999499 | ACAGTCTATCTCTCA[C/T]TTTATTTTGCCTGAA | 221178 |
rs536546332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202850 | GGAAATAAAAATGGC[A/G]TCATACGGAAGCATT | 221178 |
rs536548328 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054111 | CAGCATGGAGGAGGA[A/G]GTGAAGAAGCCCACA | 221178 |
rs536551730 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231062 | AACACTTGGCTCCCC[A/C/G]CAGAAGGCTTCCCCA | 221178 |
rs536565709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041936 | ATGTATCTGACACAC[A/G]GTCCTCGCCTTTTCC | 221178 |
rs536568724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127994 | TGCTCTGTAATTCAA[A/G]GGCTAACCCATGTGC | 221178 |
rs536570502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247762 | TGCTGGGATTACGGA[C/T]GTGAGCCACCCGCCC | 221178 |
rs536595564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148132 | GTAAAATTGTTGAAT[C/T]ATATCATTTCCCATA | 221178 |
rs536597220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220171 | ATGTTGGTACCTCTT[C/T]CTCTGTAGACAGCAC | 221178 |
rs536600760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036959 | TTTTGTATTTTTAGT[A/C]GAGACGGGGTTTGAC | 221178 |
rs536607111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292461 | CTTTTAGATGAGAAT[C/T]GAAACAGGGTCCATG | 221178 |
rs536626189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059179 | GGTTTCACCGTGTTA[A/G]CCAGGATGGTCTCGA | 221178 |
rs536626348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257005 | AAGCTTTTCTCTTTC[A/G]TTTGAGACAACTTAC | 221178 |
rs536634881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982307 | TCCACTGCAGCCTGG[A/G]AAACCTCTTTGAACT | 221178 |
rs536638842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139031 | TAAAGCAACATAAAT[G/T]AATTCTCTCACACTT | 221178 |
rs536643722 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103666 | TATAGGTGCACTAGA[G/T]GTATCTATATGTATT | 221178 |
rs536656044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148885 | TCATTCTGGTAGAGC[A/G]GCTTGTTTATTATTC | 221178 |
rs536711882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180849 | TTAATGACAGGGATA[C/T]GTTCTGATAAATGCA | 221178 |
rs536714575 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070624 | TGAACATTATTCTGT[C/G]TGTTTCTGTCAGAAT | 221178 |
rs536718232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988698 | TCATGATGGAAAATG[C/G]TGTCTCAGTGTGGTT | 221178 |
rs536724135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143684 | CACCCACAGGGAACC[C/T]GAAACGTCCTCCAGG | 221178 |
rs536726320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218948 | TCAGAAGCTTTTTTG[C/T]TTGTTTGTTTCATTT | 221178 |
rs536731192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221550 | AAGGGTTTGGACACA[G/T]ATGTGCATGATGGGG | 221178 |
rs536767252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193212 | ACAAGTGAGTACACT[G/T]AGGGGGAAGTGACGG | 221178 |
rs536774655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186960 | GAGCCTCATTATGGG[C/T]CAGATGTGTAGGTGT | 221178 |
rs536775396 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102873 | GAAATCTTTGCCAAA[A/G]CCAACATCGTGGAGA | 221178 |
rs536777338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121376 | ACCCTTGCCTCACAC[C/T]CCATTACATCTTTTT | 221178 |
rs536777659 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24252109 | GTGTCCGTGTACATA[C/T]ATTCCTGCATGTGGA | 221178 |
rs536780721 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305759 | TATTCCATTCTTCAC[A/G]TTTCAGAATTGGTCG | 221178 |
rs536784860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065337 | AAGGTTGTATGAGGG[A/G]TAGCAGATGGGAGGC | 221178 |
rs536785169 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117440 | ACAGATGATGCAGTT[A/T]GGGTTTACTGTTTCT | 221178 |
rs536785846 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126040 | GGGAGCCAGGAGCCC[A/C/T]GTATCAAACAGGCGA | 221178 |
rs536791775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228348 | TGTCGATCTCCTGAC[C/T]TCGTGATCTGCCTGC | 221178 |
rs536802208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154297 | ATCTAATTGTCCATC[A/G]ACAATAGAATAGGAC | 221178 |
rs536817554 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055365 | GGGTTCAAATCTCGA[-/C]CTTGTCCTTTTCTAT | 221178 |
rs536830485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983131 | AGAGTGTCTTTGTTC[A/G]GGCTGCCATCACAAA | 221178 |
rs536837451 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24071021 | CTGTGTTAATGTCTA[G/T]ATCTGTGTATATATT | 221178 |
rs536838534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196126 | GAGTTTTCAAAATAT[C/G]TTAAAGGGCCTGGAA | 221178 |
rs536840944 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270163 | TTAACAGTCATTTTA[C/G]AATATGAAAGACTTG | 221178 |
rs536841120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989707 | CATTATTGCCATGGG[C/T]GGAAAGTTTGTGTCC | 221178 |
rs536842963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047216 | CATCTCAGAATAACA[A/G]TCTTAGGCAATATAA | 221178 |
rs536845164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273184 | AGAAGCCCAGAGCCA[A/G]CGACGCCCCAGCTCT | 221178 |
rs536850482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082347 | GCATATATTAACAAA[C/T]GCACCAGGTTAGCTT | 221178 |
rs536869331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231731 | ACCAGCATTGTATAA[G/T]GGTTCCAATTTCTCC | 221178 |
rs536875730 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983659 | TGTTTTTTTTTTTTA[A/T]AAAACATCCAGAACT | 221178 |
rs536882799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094480 | AGGAAGGCAGAATGG[C/T]ATCTGCCAAATACTG | 221178 |
rs536909455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001296 | ATGAGAGGAGGTGAC[A/G]CCTCTGCGCTAAGGT | 221178 |
rs536911262 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082766 | CGGAGCTTGCAGTGA[C/G]CCGAGATTGCGCCAC | 221178 |
rs536913657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076371 | GGGATGATGAAATAA[A/G]TCAATGGGAAAGCAC | 221178 |
rs536919434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053737 | TTCTGTATGATTTTG[G/T]GGCTGCTGTCTCAGC | 221178 |
rs536924943 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24189218 | GGCTCATGCCTGTAA[C/T]CCCAGCACTTTGGGA | 221178 |
rs536929033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153378 | CCAGCACACTCTTCT[C/T]ACACTCCATTTCATT | 221178 |
rs536940063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012808 | AACACCACCCTGAGC[C/T]CCGTGGCTGCAGACA | 221178 |
rs536956693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197504 | ATGTTTGCTAAATTA[A/G]ACAACACTGGTTAAT | 221178 |
rs536964672 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283802 | CTTTCCAGCACATTG[C/G]TTGGCAGCATTGTTA | 221178 |
rs536976137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076819 | AGAAGGCAGTCCCAG[A/G]GGGCGTGTTCCAGCA | 221178 |
rs536989353 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168898 | ATAAAAAGCCCACAC[A/G]GTATTCTTTAAATGG | 221178 |
rs537014029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206499 | CCTTGTGGAAAACAG[C/T]GTGGTGATTCCTCAG | 221178 |
rs537017412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199260 | CGCCAGCTGCAATCC[A/G]TGTTTGCCAGCCGCT | 221178 |
rs537018395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298654 | AGTCATGGTCCAGGA[C/T]GGAGGGGAGCCAGCA | 221178 |
rs537045826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132636 | TCAGTAAGGCCAGGC[C/T]TAAGAGAAGACATTA | 221178 |
rs537049717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178392 | TACTTCTGAGGAACA[C/T]GCATTTTTTTTTAAC | 221178 |
rs537053495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017801 | TCTGTATGTTAACTC[C/T]GTAATCCATATGTTA | 221178 |
rs537057158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298077 | TATGGAACTGGCCCA[C/G]TCTTGCACTGTGGCC | 221178 |
rs537066068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219545 | ATACGACTTCACATC[A/G]AAGTTAAATCTAAGT | 221178 |
rs537070271 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104221 | TTGGATTTGTTGAAC[A/G]ATGTAAAGCTAGAAT | 221178 |
rs537075377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205857 | CCCTATTTAATAAAT[A/G]GTGCTCGGAGAACAA | 221178 |
rs537090972 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285842 | CCCACCACCACGCCT[A/G]GCTAATTTTTGTATT | 221178 |
rs537098353 | in-del | -/T | 0.00173301 | 0.0293854 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284314 | ATACGGGATACCTGA[-/T]TTTTCAGGGTCCACA | 221178 |
rs537103959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126631 | GTATGAATATGGCTC[A/G]CTGCAGCCTAGAGCT | 221178 |
rs537104060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184916 | CAAGCGACGGAGTCT[A/G]CGGAAAATGACCACT | 221178 |
rs537114986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053047 | TTGGGCTGAAAAATA[A/G]GAATTCTCTTTTATT | 221178 |
rs537125835 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087298 | AAAGCCTGCTACCCA[A/C]CCCCTGCACACTCTG | 221178 |
rs537127203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291422 | AGAAGGGGTGAGGGC[A/G]CACACAAGCTTGAAC | 221178 |
rs537136598 | snp | A/G | 0.00241351 | 0.0346545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041614 | TGATGTTAAGGAAAT[A/G]TTTTCTTTTCATTCT | 221178 |
rs537138925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106676 | TTCTGGGGCCGACAG[A/T]GCTGGCTCTCGTTCC | 221178 |
rs537141182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211361 | AAGCTTTCAGGTTTG[C/T]ACTATTGGGTATGAT | 221178 |
rs537165440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190722 | TGGAGGAGCAAAGAG[A/T]GTGGTTTCTTGTGAC | 221178 |
rs537167294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184393 | CTGTGCGGGTCCCAG[C/T]TGGGCCAAGCAGCCA | 221178 |
rs537175180 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24066707 | CACCTTCATTCCCCT[C/T]CTCACTCTTTCAAAC | 221178 |
rs537179202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277405 | CCCGAGATCGCGCCA[C/T]TGCACTCCAGCCTGG | 221178 |
rs537179492 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303199 | ATTTGATTTTCAAGG[A/G]TGCCGTCAAGACGGG | 221178 |
rs537182289 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24221537 | AGGTGTGGGGTTGAA[A/G]GGTTTGGACACAGAT | 221178 |
rs537194497 | in-del | -/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143382 | TCCTAAGTAGTACCT[-/G]GAGCAGGGTTGCAAG | 221178 |
rs537200388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101412 | TTGCTTATTTGTCAT[A/C]CAGCTTGGATACTTT | 221178 |
rs537216120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213725 | ACAACTTTAATATAG[C/T]GATCCTATTAATATT | 221178 |
rs537219090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019242 | TACAGGCGCCCGCCA[C/T]TACGCCCAGCTAATT | 221178 |
rs537236408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276870 | CAGCACCGGCCTGTG[G/T]GTCTGGCCATTGTGA | 221178 |
rs537251020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020013 | ACCTTTAAGCTCTAT[C/G]TTTATTGCACTCATT | 221178 |
rs537257239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302322 | TAAAAATTAGCTGGG[C/T]GTGGTGGCACACACC | 221178 |
rs537257389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295873 | CTGAAGCACAGAAAG[A/G]TTAAATAACTTGCCC | 221178 |
rs537257988 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185392 | TTCCTGATTCAAGAC[C/T]GTAATTTATTCTTAA | 221178 |
rs537272988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042218 | CGTTCTGTGTCTCTT[G/T]TCTTACTCCTAAATC | 221178 |
rs537292768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122298 | GAAAGATAGTTTGAA[A/T]CTATTCAAACTATCG | 221178 |
rs537297699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195509 | ACTCTATGTTTCATA[C/T]TTTTAGGAACTGCCA | 221178 |
rs537306280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128511 | TAGGAAAGTGCATGG[A/G]TCCAGGTCATGCTTC | 221178 |
rs537308270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183149 | CAACACACTCTCTCA[C/T]TGAGTCTAAACTTTT | 221178 |
rs537332681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148966 | CCACATGAGAGCAGG[A/G]CTCTGTGACTCAGGG | 221178 |
rs537334704 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159004 | TGTAAATGTTAATAG[C/T]GGTTTCCAAGTAGGC | 221178 |
rs537345591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268292 | GTATTCCATGAGATA[C/T]ACTTAGGAGACTTTA | 221178 |
rs537355336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200052 | CCCTTCCCATGGCTC[C/T]TGGTTGGTCAGTGAT | 221178 |
rs537356879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281192 | CCAAGGCTGTGGAGC[A/G]CTTTCTTCTGCCTCT | 221178 |
rs537360946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042579 | CATCTATGCCCGTGC[A/G]CGAACTCACTTCTCA | 221178 |
rs537363261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111649 | GGGCTCAAGCGACCC[A/G]CCTGCCTTGGCCTCC | 221178 |
rs537370818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122680 | TGACAGACAGAAGTG[A/T]GTCTGTATCAACTGT | 221178 |
rs537372051 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189769 | ATAATATATAATATA[-/T]TATAAATATATTTAT | 221178 |
rs537383610 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24205157 | AAGTCAAACTATCCC[G/T]GTTTGCAGATGACAT | 221178 |
rs537393850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280798 | AATGATGTGCTTCCT[C/G]AAGACATCCCCCAAC | 221178 |
rs537394687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284365 | CTAGTTCTTCTTTAC[C/T]AAGCATGTCCGAAAA | 221178 |
rs537395229 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144538 | CACAGCGTACACAAT[A/G]CACAAGCACTGGCCC | 221178 |
rs537415957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108096 | GGGGCCTTGCTGCTG[C/T]GCCCTCTGGAGGGGT | 221178 |
rs537417951 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203476 | TTTTTGTGACTGAAA[G/T]GGGACAGCACTTCTG | 221178 |
rs537422795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992063 | ATGTAACCCTCACAA[A/G]ACCTAGGAAGTGAGT | 221178 |
rs537439941 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104497 | TTTTGTATATACCCA[-/C]CATATGCAGGTATCT | 221178 |
rs537451700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165353 | GAGGACTCTACCTGT[C/T]CAATCCAGGAGAGGG | 221178 |
rs537465731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250818 | TGGGAAATGATTCTG[C/T]ACTGAAGCAAATTGT | 221178 |
rs537477138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108503 | GGGACTCTTGTGAAA[C/T]GGGACCTGCCTACTG | 221178 |
rs537478941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209263 | TTTCTCTATTAAACC[C/T]CAGTTAGGCTTTTAG | 221178 |
rs537478978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202909 | GAAGTCGACAAGCAA[A/T]CAGGAAAACCCTAAC | 221178 |
rs537494086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291825 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 221178 |
rs537501051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081556 | ACTCATGCATGTAAT[C/T]GCAGCACTTTGGGAG | 221178 |
rs537513606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171132 | TCGAAGGACCCTACA[A/G]CATCAAACGAGTGAG | 221178 |
rs537518858 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24123249 | TGAAGGGCAATGGCA[C/G]CTTCCACTTTCACAG | 221178 |
rs537533473 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24157448 | GGACTACAGGCGCCC[G/T]CCACCACGCCCGGCT | 221178 |
rs537540402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109224 | TTTGGTTTTCTGTTC[C/T]TGTGATAGTTTCCTG | 221178 |
rs537572276 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139849 | AAGGAGGGCGGATAA[C/T]GAGGTCAGGAGATCT | 221178 |
rs537572506 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24084130 | TAGAATTGTAATGAG[C/T]TCCCAAGCCTGATCC | 221178 |
rs537576439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170749 | GGGCCCTTGTTCCCC[A/G]GAACTGGGACAGCCA | 221178 |
rs537580493 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255686 | GTCACATGGGAGATG[A/C]AGCCCAAGGGGTGGT | 221178 |
rs537581581 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105316 | ATTTTTTGTATTTTG[C/G]GGGGTAGAGACGGGG | 221178 |
rs537587608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177062 | GAGCTGCCGCACCCA[A/G]CCTGTAGTATATACT | 221178 |
rs537593539 | in-del | -/TGTA | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179140 | TGAATGATACTTCAT[-/TGTA]TGTATGTACCTCATT | 221178 |
rs537605911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028643 | TTGATAACTACTATC[A/G]GTTTTGGAAAATTCT | 221178 |
rs537615674 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214519 | ATCCCATGGAGAAAG[A/C]TGGGTTCAGGGATGT | 221178 |
rs537619536 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155573 | CAGGGCTTTCAGAAC[C/T]AAGCCAGAGTCAGTG | 221178 |
rs537625462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294203 | GGAAAGCACCAGAAA[A/G]GAAGATCTGTTGGTG | 221178 |
rs537638414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180529 | CAAATCATGCAAAGT[C/T]GTCAGCCAGGATTTT | 221178 |
rs537641375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054255 | TTCATTTAGCCAGGA[A/G]AAGGGAAGAAATCTT | 221178 |
rs537641466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060856 | TCAGCGTGGCCAACA[C/T]GGCAAAACCCCGCCT | 221178 |
rs537649099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183731 | ACACCCCTGCTTTAT[A/G]ATGTTCTCTATGGGC | 221178 |
rs537656263 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134502 | CTTTTTGGCAGCTTA[A/C]GCCAGGCCTGGATTA | 221178 |
rs537662265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293808 | TGCTTGGTGGGCAGT[A/G]TCTGGGGACTTCACA | 221178 |
rs537665344 | snp | A/G | 0.000231669 | 0.0107602 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224008 | GCCGGCTGCATGACG[A/G]CTACTCCCGCCGCGT | 221178 |
rs537695165 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24066619 | GGTGCTCACTGTGCT[C/G]ACAATGGCTCCTTTC | 221178 |
rs537709334 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989380 | TGAGCCGAGATCACG[C/G]CACTGCACTCCAGCC | 221178 |
rs537737142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299421 | GCCTCGAATATTTTG[A/G]CAGCCCTCGTACTTG | 221178 |
rs537738670 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305577 | CACGTGTTCCACTTG[A/G]AAAGAAAGGGAACAG | 221178 |
rs537758656 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068969 | AGGTTGTTTGTTCAC[A/T]CTGTTGATAGTTTAT | 221178 |
rs537772037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129051 | TCACCCTGTGGCACC[A/G]CACCATCTGTTTGTT | 221178 |
rs537792495 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089799 | ACAACAGAAATGTGT[G/T]TCTTGTGGTTCTCGA | 221178 |
rs537792977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039744 | CTGCATGTGACTGGG[A/G]TTGGGGGAATTCTGT | 221178 |
rs537793268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278283 | CACAGCTGTGTGTTA[C/T]TGGGACTTGAGTTTC | 221178 |
rs537838090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045635 | GAAATAAAATCAGTC[C/T]TCAAGGGAAGTCGAG | 221178 |
rs537852676 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098756 | ACATGGTGAAACCCC[A/G]TCTTTACTAAAAACA | 221178 |
rs537855570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248195 | AGACAACTGCTCTCT[C/T]ATCAGGCCTGATCCC | 221178 |
rs537855925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169469 | GTCTGGGTTCTATTT[G/T]TTGTATTTCTGACTG | 221178 |
rs537858113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241527 | GCATGGGTAACGGGC[C/T]TTTATAGGAGCCCCT | 221178 |
rs537860119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073388 | TAATTTTGTTACTTG[C/T]TTTCTATTTGATACA | 221178 |
rs537875118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277404 | ACCCGAGATCGCGCC[A/G]TTGCACTCCAGCCTG | 221178 |
rs537881795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272050 | GTAATGCTAGCGAGA[C/T]GGCACTGGCAAGACC | 221178 |
rs537886559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283931 | TGGCAATACACTCTT[G/T]AACATTCCACCTCTC | 221178 |
rs537889785 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24008519 | ACGGTCTTGTTGGTG[A/G]TGACTTCAGATAAGA | 221178 |
rs537910664 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168978 | TTGTTGTTTTCTTTT[C/T]TTCTTTTTTAGATTT | 221178 |
rs537912605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146746 | ACCTTTGTGTCTAAA[A/G]CATTTTCCATCGTGG | 221178 |
rs537914706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068107 | TTATTTCATCACCCA[A/G]GCATTAAGCCAAGTG | 221178 |
rs537917592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247778 | GTGAGCCACCCGCCC[A/G]GGCTCTGCATCCACT | 221178 |
rs537917950 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996290 | CACTAGAGTTTGCAA[A/G]TGAGAAGAAAAGATC | 221178 |
rs537921609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288834 | TATTTTAAAACACCT[A/G]TGGCAAATTGCAGTC | 221178 |
rs537930186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161460 | GAGTCTCGTCCCAGG[G/T]GAAAGATTTTGGGAC | 221178 |
rs537948655 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24135614 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 221178 |
rs537949936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986286 | TTTGTATCTTGAAAA[C/T]TGGGGCATCTAAGAA | 221178 |
rs537963252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277227 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 221178 |
rs537973318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284798 | GTGTTCGGCCAGTGC[C/T]TTCCACTTGATAAAG | 221178 |
rs537992040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147317 | CAGTGAGTGTAGTCT[A/G]CTTTGCTAAATGTGA | 221178 |
rs537996470 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24160538 | CAAGAGCCACTGCGC[C/T]TGGCCGGGGAACTGT | 221178 |
rs538003698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247251 | GGGGAAGTTGCTGGA[A/C]CCTGCACGGGATTGT | 221178 |
rs538026097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115854 | CAGGTCAGTGCTGGT[A/G]GCTGGCAGGCAGCCT | 221178 |
rs538032648 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979914 | AGGACGTAGGAGGGA[C/T]GCTGAGACAGGCAAG | 221178 |
rs538039715 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24079873 | GTGAGGATGGGGATA[C/T]TCATACACTGTCTAC | 221178 |
rs538040024 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137089 | CCCGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 221178 |
rs538054623 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192757 | GATTTGTTGTGGAAG[C/G]GGTGCCATGGAGACA | 221178 |
rs538055954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167519 | TTCCTCACCTCTCAA[A/C]AGTACAAGCTTGAAT | 221178 |
rs538086903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200560 | TTCGGGGATTATCAC[C/T]ACTTAACTCTTCTTT | 221178 |
rs538089012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036883 | TGGGTTCAAGCGATT[C/G]TCCGACCTCAGCCTC | 221178 |
rs538100021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179906 | TTATATATCCTGGAT[A/G]GCAGACTCCTATCAG | 221178 |
rs538101417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251921 | ATCTGACCGTTTCCA[A/G]CTAACCTGAGGCAGC | 221178 |
rs538101812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273489 | TGAAGAATGGCTTGA[A/G]AGTCTAGATTAGATA | 221178 |
rs538104428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258188 | TGCAGTGAGCCTACA[C/T]TGCGCCATGGCACTC | 221178 |
rs538117906 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166920 | CTTGGGGTTTAAATT[A/T]CAACATCAAAATTTT | 221178 |
rs538119526 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142854 | CTTGGAAGAGTGTTT[C/T]CCTTCCCCTGGGGAG | 221178 |
rs538123291 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117340 | TTGTCCAGGTATTCT[A/T]CTCCCTTGTCCTGGC | 221178 |
rs538129464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246408 | TGGGGAGGAAAAAAA[C/T]GTTTCCTCTACACTC | 221178 |
rs538135169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228153 | GAGTCTAACTGTGTC[A/G]CCTAGGCTGGAGTGC | 221178 |
rs538138888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220775 | CCCGGGTGGAATCAA[C/T]TCTTTGACCCTTTAC | 221178 |
rs538140161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127117 | AGTGTTGAGGTAGAA[A/G]TGCCAGTCAATCCTG | 221178 |
rs538182963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086124 | GCCATAAATGCCACC[C/T]GGTGAGTTTGACTTT | 221178 |
rs538192705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178846 | TTTAGTGTATCCACG[C/G]AGTCATGCACTCATC | 221178 |
rs538201602 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154826 | GTGTCGACAGAATTC[A/C]CTTCTTTGGAGCTGT | 221178 |
rs538203512 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227284 | CAGAATTATTTTTTT[A/T]AAAATCATTGAAATA | 221178 |
rs538220899 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24282170 | AGCATGATGGTGGGG[G/T]GTGGGAGTCTGGGGC | 221178 |
rs538227389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028352 | GTATCAGTTCATGTG[C/T]AGGTGTCTATATTTT | 221178 |
rs538246323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086540 | TCAAAAGACAAGTTC[A/G]ATGGCTGGGTCTGTA | 221178 |
rs538268103 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182436 | AAGCTTCCAGTCACA[G/T]TGGGAGGTGAAGGGG | 221178 |
rs538298811 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24014364 | CCATGCAGAAATGGC[C/T]CCACTGTTTCTGGGG | 221178 |
rs538301558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237517 | TAGAGACAGAAAGTA[A/G]AGTAGTCATTGCCAG | 221178 |
rs538336711 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098345 | GGAGAATCTCTTGAA[C/G]CCAGGAATTCAAAGT | 221178 |
rs538343439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104155 | CTGCTCACCACATGT[A/G]TACGTGCTGAGAAAA | 221178 |
rs538344325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197055 | CCAGCAACAGCAGGT[A/G]GCCAAATAACAACCA | 221178 |
rs538346317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115478 | ACCCTATTGCAAACC[A/G]CGCATGCGAAGGATG | 221178 |
rs538361044 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24261342 | GAGCATGTTGGTCAA[C/T]TGGGGAGCTTACTCC | 221178 |
rs538369514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275022 | CTCACCAGGACTACC[C/G]TCCCCCACTTATCAG | 221178 |
rs538374248 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24262580 | TGGGTCAAAAAGTGA[C/G]AGTGTAATCCCAATC | 221178 |
rs538391054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036241 | GACAATGAGTAGGAA[C/T]GACAGTGTTTTGGTG | 221178 |
rs538398427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098797 | CTGGGCATTTTGGTG[C/T]GTGCATGTAGTCCTA | 221178 |
rs538401389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236553 | GTGAGCCAATATTGC[A/G]CCACTGCACTCCAGC | 221178 |
rs538402771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201000 | CTAAGGGCTTTGCAC[A/G]CTCATGTGAATTTTA | 221178 |
rs538407616 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092279 | GTTTTCTGGACATTC[A/C/T]GGCAGCTCTCTAAGG | 221178 |
rs538423588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023335 | CTGTGAAAGCTGTAG[A/G]CATTAAGGCATAGCT | 221178 |
rs538428606 | in-del | -/CT | 0.349452 | 0.229367 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254197 | CTGATTCACTGTGGC[-/CT]CAGGACTGTGAACTC | 221178 |
rs538443764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246664 | GGAGTTCGAGACCAT[C/T]CTGGCCAACATGGTG | 221178 |
rs538445606 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069521 | TAAGAAGCTTTTGGT[C/T]TGAGATTGGGTTTCC | 221178 |
rs538454563 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105427 | TACAGGTGTGAGCCA[C/T]TGCGCCTGACTTCTT | 221178 |
rs538455228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011002 | TTCCCTCTCTGCCTT[A/G]CTGCTTTCTTCTGTC | 221178 |
rs538468347 | in-del | -/GG | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138859 | GCCTCCCAAAGTGCT[-/GG]GGGAACACAGGCATG | 221178 |
rs538469442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104248 | GAATGGGTTTTTTTT[G/T]TTTGTTTTTTGGGTT | 221178 |
rs538471979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141150 | CTGCACTCCAGCTTC[A/G]GTGGCAGAGTGAGAC | 221178 |
rs538499853 | snp | C/G | 0.000399281 | 0.0141238 | missense | SPATA13 | GRCh38.p7 | 13:24249744 | GCTCCAGTGGGCTGC[C/G]CCAAAGGAGCCCGGA | 221178 |
rs538505289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994458 | AAGGGCAGAACTTTC[C/T]GTTAGAATAGAAGCA | 221178 |
rs538508366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292910 | CTGAGGCACGAAAAT[C/T]GCTTGAACCCAGGAG | 221178 |
rs538517249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023725 | TTGCTGGCTTTGAAG[A/G]TGGAGGCCATGAGCC | 221178 |
rs538530882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213215 | ATAGGGAGGAGAGTC[A/G]CAGGATGCCAGAGAC | 221178 |
rs538532958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207202 | GTGGGGAACAACACA[C/T]GGTGGGGTCTGTCTG | 221178 |
rs538535808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981645 | GCGTTGTGGGTTTTG[C/G]TCTTTCAAGGCAGGC | 221178 |
rs538561685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121148 | ATACCACCTTTCTTA[C/T]TTTTTACAGTAAGGT | 221178 |
rs538562473 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138317 | TCTGAAAAAAAAAAA[A/C]AAAACAGTTTTACTG | 221178 |
rs538592937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170068 | AGAAGTGAGAATGGT[G/T]TGACAGTACAAGGTC | 221178 |
rs538598874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087116 | TTGTGCCCAGCAAGG[A/C]TTTCTCTCCAGCCTC | 221178 |
rs538600242 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24224087 | TGGGACCACTGCAAC[C/G]TGCACCGTGGCCCCC | 221178 |
rs538638032 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288433 | TACAGCCTTTTCTTC[G/T]TATCCCACTAGCTCC | 221178 |
rs538705384 | snp | A/C | 0.498158 | 0.0302955 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137129 | GCCACCGCGCCCGGC[A/C]TGTTCTTTATTTTTA | 221178 |
rs538708404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022574 | TTTACTGAGCTGCAC[A/G]CTTGAAAATGGTTAA | 221178 |
rs538712603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237258 | GCTACTCAGGAGGTG[A/G]AGGCTGAGGCAGGAG | 221178 |
rs538715918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000746 | CTCTGGGTCAGAGGC[A/G]TGAATTTGGGAGAGC | 221178 |
rs538719723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230737 | TCAGGGAGCTGCAGA[C/T]GGCTTGCAGAACTTC | 221178 |
rs538726106 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24243559 | TCTGGCTCTATTAAC[A/G]TGAGCAAATCATTTC | 221178 |
rs538731360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036901 | CGACCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC | 221178 |
rs538735104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980404 | GTCACTGCGTGAGCC[A/C]CCACTCTGATGCTTC | 221178 |
rs538748909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280666 | TCAGGATATCTCGGC[A/C]AGTAAGCAGCACAGT | 221178 |
rs538749171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058108 | ACATTGGAGTGTTAT[A/G]TCTTTGTATTTATTT | 221178 |
rs538751503 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291849 | GCAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 221178 |
rs538762067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267407 | AATAATCTCTAGTGA[A/G]TGCCTCTGGCTTAAG | 221178 |
rs538769759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137689 | GCTTGAGCCTGGGGG[G/T]CGGAGGTTGCAGTGA | 221178 |
rs538773149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244581 | TGTATGCGGAGTGGC[C/G]AGGCACTGTGGTTCA | 221178 |
rs538782442 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307304 | CGTCAGTGGTTGGAG[C/T]AAGAGGGATGCGGAA | 221178 |
rs538786442 | in-del | -/GTCATTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24266715 | CAATAATCAATGATG[-/GTCATTT]GTCATTTCCCAGTTC | 221178 |
rs538787636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285612 | ACCTCCGCCTTCCAG[A/G]TTCAAGCAATTCTCC | 221178 |
rs538803589 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997337 | CACGCATGTCCCCTG[G/T]GATCCGACCGTCCCC | 221178 |
rs538810068 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229704 | GACATCATGCTACTT[A/T]AAAAAAAAGCATAAG | 221178 |
rs538816422 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030106 | TACATACATACATAC[A/G/T]TATACCCTCCCCTAT | 221178 |
rs538819136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198724 | TGCCAAGTCTGGGTC[A/G]TCCTGTGAGGGCTAT | 221178 |
rs538835505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051645 | GTTTGGGGATGGAGG[A/G]GTGGGGACTTAGGGG | 221178 |
rs538838015 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24063065 | CCCTGGGATTGGCCT[C/T]GGGGTCACCTGCCTG | 221178 |
rs538862764 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122234 | TGTTCTTCAGAAAGA[C/T]GGTGAGTCAGAGCCT | 221178 |
rs538873875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052104 | TGCTGTGTCCAGGCT[C/T]CTCGGGTCTCTGTGC | 221178 |
rs538877227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126027 | ACGAATAGAGCAGGG[C/G]AGCCAGGAGCCCTGT | 221178 |
rs538890334 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24251319 | CCACCCTGGCCGGGT[A/T]TGTGGCCTTGTCCTG | 221178 |
rs538899249 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105404 | TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 221178 |
rs538904138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086571 | GCCTTGGGGACTGGC[A/G]AGAAGGTGGAATAGA | 221178 |
rs538907020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193269 | GAAATGGACAGGAGG[G/T]AATGACTCCAGTGAG | 221178 |
rs538910705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139093 | GCTCCGGGGGTGCAT[A/C]CTTCCTCGCCTCTTC | 221178 |
rs538921736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290588 | GAGGGCTGGGATGAT[A/G]CCTGTCTTTGTCATG | 221178 |
rs538932427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210563 | AGTTAAGTTGACCGT[A/G]TATGCATGGGTTTAT | 221178 |
rs538934810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065305 | TCAGAGTGGGGGTTT[A/T]GATGTGTGTGGTGGA | 221178 |
rs538935629 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24073124 | CATTTTCTGGATAAC[A/G]TCATGATCATTAGGT | 221178 |
rs538939480 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24237864 | AAATATATCACATAT[A/G]TTATATAATATATAT | 221178 |
rs538939545 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23995658 | TAATTTTGTAATCTG[A/G]AAAGTTTTGATTCTT | 221178 |
rs538941523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204273 | ATTTTTCATTTTGCA[G/T]ATGAAAAATCTGAAG | 221178 |
rs538946795 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046280 | ATCCTGACTTCTAAC[A/C]CCATAGATTTCTTTT | 221178 |
rs538947038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157055 | CTCTGAGTGACCTCC[C/T]AGCTCCTTTGCCTCT | 221178 |
rs538950997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235171 | CTTCTAAGTTATAGC[C/T]GGAGCAAAGACCTCG | 221178 |
rs538956986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005083 | AAAGAGCTAAGAGTT[C/T]CTCAAAGTAAGTACT | 221178 |
rs538957392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024679 | TTTGTTAATATTTGA[C/T]GACATAAAAATGTTA | 221178 |
rs538971366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198148 | TTACAGGCGCCCGCC[A/C]CCATGCCAGCTAATT | 221178 |
rs538972601 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133329 | TTGTGTAAGCCCAGT[G/T]GGAAATAGTGGCTCC | 221178 |
rs538974655 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24094744 | CCACTGCACTCCAGC[A/C]TGGGCAATATAGCAA | 221178 |
rs538981176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041433 | AAATGACTCAGAATC[A/G]GAATCTCACATGTAA | 221178 |
rs538990071 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081789 | AGCTCATTCCCCTGT[C/T]GGCTTCACAGCCATT | 221178 |
rs539027920 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251953 | GGTTCTGCACCTTCG[C/T]GCCTCCCTTGGGCCA | 221178 |
rs539032040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122905 | AGCAGATTCCCTCGA[A/G]CTGTTGGGTTATCTC | 221178 |
rs539035651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295130 | CTCTCTCCTCGTAGA[A/G]GGAGTACCGTGGGAA | 221178 |
rs539052139 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24229437 | GTCTTCTCAAGGGTA[G/T]GATATGGAGTAACTT | 221178 |
rs539065431 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299315 | TGCTCCCTGTGGCCA[C/G]TGCTCAGAGATGCAA | 221178 |
rs539079439 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24097493 | GCTCAAAGGCAAAAA[C/T]ACTAGATTCTGGGGA | 221178 |
rs539126714 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115399 | AGAAGGTGAGTGAGC[A/G]TTACTGCCTGAGCTC | 221178 |
rs539138881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150766 | TCAGGGAACCCACAT[A/C]TTCTCTCCTATGACT | 221178 |
rs539151361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300775 | TCCCCCAAGTGCTGA[C/T]GGTGTTAGCCACAAG | 221178 |
rs539153218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245729 | CCCAAGTAGCTGGGA[C/T]GACAGGCACATAAAA | 221178 |
rs539157943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188080 | GCGTGGTGGCTCATG[C/T]CTGTAACCCTAGCTC | 221178 |
rs539164516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038403 | TGGTTATTTTTGATA[C/T]TCCAACATAGTCTGT | 221178 |
rs539171239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113207 | ACGTGCCAAAGGAAA[A/G]CATATTTTTACATCA | 221178 |
rs539201797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033536 | GACCTGGAAGAAGAC[C/T]CTGAGGAGAACCCGG | 221178 |
rs539204009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226224 | GCCCTGAGGCTTCAG[A/G]CTGTCCCTGGCTTGA | 221178 |
rs539206562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064700 | TGGCTCTAAGCTACC[C/T]AGTCTATGGTACTTT | 221178 |
rs539208381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219649 | ATAATCCATTTTGGT[A/G]AAAACAATTTGATGA | 221178 |
rs539209788 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24177692 | CTTGAACTTAAGTGA[A/T]CCTTCCACCTTGGCC | 221178 |
rs539214872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266553 | GCCTCCCAAAGTGCT[C/G]GGATCAAGGCATGAG | 221178 |
rs539225349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274197 | ACTTGTGGCTTGCTG[C/T]ATGGACAGGCAACAA | 221178 |
rs539225749 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070525 | TGATTGATTAGCTTC[A/G]GCCTTACTTTGGGAC | 221178 |
rs539241650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213516 | ATGATCCATCTGCCT[C/T]GGCCTCCCAAAGTGC | 221178 |
rs539242655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235607 | TCTTAAAAAAAAATA[A/G]AAAGCCAGGTGTGGT | 221178 |
rs539245697 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066965 | ATAATAGCTAAAGCA[G/T]CTTCTGTTAACCTCA | 221178 |
rs539249534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191319 | TTTTCAAACATAATG[C/G]TATTACACACATGGT | 221178 |
rs539253523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263647 | ATGTAAATAGTTGTT[A/G]TGCTGCATTGTTTAG | 221178 |
rs539255093 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140272 | CATTGTAATCTGTGA[A/G]CACCACGGTGGGTTC | 221178 |
rs539262976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273939 | AAGCAATCCTCCTGC[C/T]TCAGCCTCCTAAAGT | 221178 |
rs539263323 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016610 | CAGTGTCCAGGGCCC[A/G]GGCATGGCCTGCAGG | 221178 |
rs539272203 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303703 | CTGAGGTCAGGAGTT[C/T]GAGACAAGCGTGGCC | 221178 |
rs539289464 | in-del | -/TTGCAC | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122643 | TTTTGCACATACTGT[-/TTGCAC]ATATCACTTCAAGAT | 221178 |
rs539291760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059193 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 221178 |
rs539291840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982521 | GAGTAGAACTAATAC[C/T]TTTATAGATACTATC | 221178 |
rs539299435 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027155 | TTTTTTTTTTTTTGA[G/T]ACGGAGTCTAGCTCG | 221178 |
rs539308820 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058654 | TATGAAATTCAGATA[A/C]TTTATTAGTTGCTTA | 221178 |
rs539312344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017995 | GCACTATTGCTACTA[A/G]ATGTTCTGCTAGTGT | 221178 |
rs539312930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989079 | GCTGAAGAAAGAATA[A/T]CTTTGTGAGAAAGTT | 221178 |
rs539333796 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020996 | CACAGGGCCTAGATC[G/T]AGACACTGCACTCCA | 221178 |
rs539341442 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154980 | CTCATGCCTCAGCCT[C/T]CCTTGTAGCTGGGAT | 221178 |
rs539341939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260456 | AGTAGAGTTGTATCC[G/T]CACCGGGAGTCAAGA | 221178 |
rs539356733 | snp | A/G | 1.90011e-05 | 0.00308224 | intron-variant, synonymous-codon | SPATA13 | GRCh38.p7 | 13:24278814 | ATGTGCATCGCTATC[A/G]TTTGAAGGCAAGTTC | 221178 |
rs539378681 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990379 | GCCCTGGCTCACTCC[C/G]TCTGTTTCCTTGCTC | 221178 |
rs539410722 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287600 | CACTATCTGCAACCC[C/T]GCTGCATCTAATCAC | 221178 |
rs539412621 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293661 | AAACTTATTTTGCGA[A/C]CCTTTCTTCATTGCT | 221178 |
rs539422161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173152 | GTGCGATCTTGGCTC[A/T]CTGCACCCTCCGCCT | 221178 |
rs539442988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077731 | GTAGGCCCCAGGACC[A/G]TGTATAATCCATACT | 221178 |
rs539449388 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293026 | AAAAAAAAAAAAGGC[G/T]AGGGTGTGGGGAGAG | 221178 |
rs539455580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213269 | CAAAGGGTCTTTTTT[C/T]GTTTGTTTTTGTTTT | 221178 |
rs539462124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166722 | CAACCACAGAAATAT[A/T]TGAAAGCCACTGTTT | 221178 |
rs539462397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090660 | CTGCCCCAACTTACT[A/G]ATGTTCCCTATTTGA | 221178 |
rs539484531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050257 | AAGTATAATAGATAT[C/T]AAAAAATAGAAAGTT | 221178 |
rs539485150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057284 | TGGGAAATGGAACTT[A/C]TTAATCTCGGCCACT | 221178 |
rs539490085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257328 | TGCACACCCGTGCAC[C/T]AAAGTCAGTCGATAT | 221178 |
rs539495496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997123 | TGGGCTCTTGAATAT[C/G]ATGACTTTTCTGCTT | 221178 |
rs539502737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078534 | CATAATGTGACTTTA[A/C]GTATGCTCACTTAAC | 221178 |
rs539502944 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24279515 | GGGAGCCCGAAGCTG[C/G]ATGGGAACCCAGGCT | 221178 |
rs539510302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298728 | ACTAAAAACCAGGAG[A/G]TGCTTTTTCTGTCCT | 221178 |
rs539548235 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304158 | CCATGTCACGTGAGC[A/G]TGTCATCAGGCTTCT | 221178 |
rs539555472 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206609 | TATAAAGATACATGC[A/G]GGCCAGGCACGGTGG | 221178 |
rs539562320 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151571 | GGTTTTGTAATAAAC[A/G]TTTCAAATTATGAAT | 221178 |
rs539573012 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044376 | TAGCTGGGACTACAG[C/G]CACCTGCCACTGCGC | 221178 |
rs539589640 | in-del | -/A | 0.354019 | 0.227333 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190366 | TATATATTATTATAT[-/A]ATAATATATAATATT | 221178 |
rs539591741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997526 | ATGGCTTTTCATTGC[C/T]TAGTAGTTATATTAG | 221178 |
rs539605391 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131741 | AAGGATAGGGACAAC[A/C]AATGTGGACCCTGGC | 221178 |
rs539610759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072627 | CATGATTTCATTGAA[C/T]CTGCCTTCTGGATTT | 221178 |
rs539615620 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144800 | CAGCCTCGTGCAGTA[C/T]GGTATGCTGAGCAAA | 221178 |
rs539623360 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145848 | ACTTCACGGCGGAGA[C/G/T]AGAGCACAGCTGGGG | 221178 |
rs539635057 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175223 | CAGTAGTGATGCTTG[-/T]TTTTTTTGTTTTTTT | 221178 |
rs539641092 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177865 | AGGATTTCAACATAT[G/T]AATTTTTTTTTAATT | 221178 |
rs539647132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297150 | CTCAGGGGATCCTCC[C/T]GCTTCAGCCTCCTAA | 221178 |
rs539670098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102270 | CCTATTGTCTACTTG[C/T]GTATCTTCTTTAGAG | 221178 |
rs539672439 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067555 | TAGAGCTGTAATAAA[C/T]ATCAAATTTAAAATC | 221178 |
rs539695396 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24059515 | ACACTAACGCTTTTG[C/T]TTCTGAGGTGGAATC | 221178 |
rs539712117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080356 | CTGTGAAGAGAATAA[A/G]CAGGAACCAACGACT | 221178 |
rs539713849 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24234500 | AATTGCTTTCAACCC[A/G]GCTTGGTGACACCGA | 221178 |
rs539725403 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993619 | CCCAGCCCTTCCCAC[A/G]GACCCCTGCGTGACA | 221178 |
rs539729255 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040442 | AGTATGGAGTGTAGA[A/C]ATTCACAGCACCGCC | 221178 |
rs539739455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218111 | CATTCAACATCTCCT[C/T]AAAGTCCACAGGCAG | 221178 |
rs539756442 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108665 | TTTTCATGGTAGGGG[C/G]GGGGAAGCCTGATGC | 221178 |
rs539771262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074043 | TTGTGGTAAGATGCA[C/T]ATACATTTTCGATCT | 221178 |
rs539780661 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023266 | GACATGAACTCATCC[-/T]TTTTTATGGCTGTAT | 221178 |
rs539787662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021344 | TAAGAGAATATCAGG[C/T]ATAGGGCAGACAGTG | 221178 |
rs539800344 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24153645 | ATAATCACAGATCCC[A/C]TACCCATGTCAATTG | 221178 |
rs539813552 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144721 | CTTTGGCCAGCGTGG[C/T]GTAGTTGGTGTTTTC | 221178 |
rs539850378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246106 | CAAAACAAACCAGAC[C/T]CCAAAAAACTAACTA | 221178 |
rs539850494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015558 | AGCTGAGTCAGGCCT[A/G]ACCCTGAGCCAGGGG | 221178 |
rs539854652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097594 | GAACAACTCATGGAC[A/G]ACACTTACAGCAAAA | 221178 |
rs539874139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130419 | CCGATTAGAGAGAAG[C/G]CATGAATCAGAGAAG | 221178 |
rs539880995 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24023700 | TGCAGTGTGAGAACC[C/T]GATCTGACATTGCTG | 221178 |
rs539895008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101706 | TAGAAGTGGAATCAC[A/G]CACCTATATAAGTGG | 221178 |
rs539897847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091260 | GGGCATACACACAGC[C/T]GTGCACATGGGTGTG | 221178 |
rs539899701 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305349 | TAGAGTGTGAGGGTC[A/T]CTCCATTAAAGATCT | 221178 |
rs539914674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134743 | CTGAGCCTAGAAAAC[A/G]TGAAGGCTTTGTTCA | 221178 |
rs539919368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234653 | CTTCTGACAGTCTGG[A/G]GACAAAACCACCACT | 221178 |
rs539924642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027279 | AGCTGGGATTACAGG[C/T]GTGCGCCACCACACC | 221178 |
rs539927322 | snp | A/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158872 | GCCTCAAGGATGCGG[A/G]GGTCTTCAGGTCTAG | 221178 |
rs539934105 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133377 | ATTATAGAAAATAAA[C/G]TTATATTTCTCTGTG | 221178 |
rs539935988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124555 | TTCTGGTGAGAATGG[C/T]AGTCCTGGAGGTGAA | 221178 |
rs539936737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009386 | CATTCTGAGCCAAAT[A/T]TGAGTGACCCATGAG | 221178 |
rs539940177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055807 | GATGTCCTAATTCTA[A/G]GCCAAGTGGGCTCTG | 221178 |
rs539948661 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281243 | GGAATTTACTCCTCC[A/C/T]CCTCCAACCCCGTCT | 221178 |
rs539953596 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978051 | CTGGGATTACAGGCA[C/T]GCATCACCACACCCG | 221178 |
rs539961650 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289259 | GAAAACAGGAGTCTC[-/TT]TTGTTTTATTGTTTG | 221178 |
rs539965468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190795 | GACAACAAAGGATTT[A/G]GAATATTACATAAAT | 221178 |
rs539971859 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009980 | TACAGGCAGTCCTGA[C/T]AACATGTGCACAAGG | 221178 |
rs539982442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055328 | TGCATCGTGTAAGAT[C/T]CCAGATGCAATCAGC | 221178 |
rs540002812 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115726 | TGCCTGTGTGCTTCC[A/G]GTTCCAGATTTCTCA | 221178 |
rs540010786 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23989886 | CACTATGTGAGGATG[A/C]AGTGAGATGGTACCA | 221178 |
rs540014176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120031 | ACAAGAAACAATCAC[C/G]AAATGGCCGTTGTTC | 221178 |
rs540015603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280428 | TCTTCGAGGAGAAAG[C/T]GTCATTTTTCAGAGC | 221178 |
rs540018567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014313 | TCATCATAACTAAAG[C/T]TGACAACTCGGGGGC | 221178 |
rs540025676 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114385 | TGTGTGCACATGCGC[A/G]TGTGTGTGCATGTGT | 221178 |
rs540035401 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129280 | AGTACAGCGTCTGTC[C/G]CATGTGAGCATGAGG | 221178 |
rs540073243 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24134666 | ATTTAAGAACCACTG[A/G]CTTGTAAGAGCAGCT | 221178 |
rs540074661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202246 | TTATCCTAGGATTTA[A/C]GTGCAAAAGGACGTT | 221178 |
rs540082450 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999082 | AGGCACATGCCACCA[C/T]TTCAGGCTAACTTTT | 221178 |
rs540103550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049840 | AGGAAGAGGGAAATC[A/G]GATTCTTTCCATTTG | 221178 |
rs540116633 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303028 | ACTATGAGATGGCCC[A/C]GATGTGGGACCCGGT | 221178 |
rs540120045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034707 | CAATCCCATAGCTGC[C/T]AGTGGGTACGGCACC | 221178 |
rs540136309 | snp | C/T | 0.000116218 | 0.00762205 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224614 | GGTCCCTCATGTGGG[C/T]GACCCTCCTGCGGGA | 221178 |
rs540139865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043980 | TGCTTGGAGGTAAGA[G/T]GATGGATTTACACTG | 221178 |
rs540141562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050303 | ACAAAAGACTAAAAT[C/G]TTTAATGCACTCTAG | 221178 |
rs540154974 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258481 | AGACCAGCCTGGCCA[A/G]CATGGCAAAACCCCA | 221178 |
rs540155678 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084308 | TCTGTGCTTGCAGTT[C/T]TGCTTCTTTTGAGAA | 221178 |
rs540162276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173771 | TTACACTGATTAATT[C/T]TCAAATACTGAATCA | 221178 |
rs540166988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146772 | CGTGGTCGGCTATGC[C/T]TCCTGCAGTCTCAAA | 221178 |
rs540167240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252775 | ATTTATTGGAAGGGG[C/G]CCAGGTGTGCCCAGA | 221178 |
rs540177474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118975 | CAGTGGTGTGATCTC[A/G]GCTTACTGCAACCTC | 221178 |
rs540191506 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306832 | AGGCTTTGGGCAACA[C/T]TTTAGCTCATTAACT | 221178 |
rs540197067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265839 | ATGTTCCTGGGTTCT[A/G]GATATGTCTGTACCA | 221178 |
rs540210211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990664 | CTATGCTATAATTGT[C/T]TACTTCCTTGTATAA | 221178 |
rs540221756 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043117 | ATCTCTCCTTCAGCT[A/T]AGGTCACATAGAGGA | 221178 |
rs540224826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044606 | AATACATGTTTACAT[C/T]GTTTAATGATCGAAT | 221178 |
rs540226487 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24173497 | TACGCCTTTTATTCC[C/T]CCCCGTCCCCCAACT | 221178 |
rs540226945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173259 | ATTTTTTGTATTTTT[A/T]GTAGAGATGGGGTTT | 221178 |
rs540240129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066635 | ACAATGGCTCCTTTC[A/G]TGCCAGCCCCTGCCT | 221178 |
rs540247081 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181218 | GCTGTTCGCTGCTCT[-/A]AAACTTTAGAAATAC | 221178 |
rs540256497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038926 | ACAAATCCAGAGAAA[A/C]CTGCTCATCCCAGGC | 221178 |
rs540268977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107613 | ACTCTTATATTTATA[C/T]GTCTGTGAATTCCAC | 221178 |
rs540282188 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997745 | GGAACAAGGGAGTGA[G/T]GGGGAGGTGCCAGCC | 221178 |
rs540293134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984787 | TATCCCAGCCAAAAA[A/T]GACTGCCTATTTCTG | 221178 |
rs540305715 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24132804 | CATGATGAAACCCCA[C/T]TTCTACTAAAACTAC | 221178 |
rs540316162 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24155760 | CATTCATATTGTTAT[A/G]CAACCGTCACCATCA | 221178 |
rs540332279 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102397 | CTCTTCATCAAATAC[A/G/T]TGGTTTGCAAATATT | 221178 |
rs540351847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264565 | ACAAAACACAATATT[A/G]TCTAATTGATTTGCA | 221178 |
rs540363176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162782 | CTCAGAGGAGGTAAC[C/T]GGCATGGCTTCTTGC | 221178 |
rs540365244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061638 | AAACCAAATACTATA[C/T]GTTCTTACTTATAAA | 221178 |
rs540369046 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151226 | GTGATTGTGGGCATG[C/T]GTCCTTCAGCATTCA | 221178 |
rs540369516 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156212 | CAGAAGAGGGATTGC[G/T]GGATGATACGGTAAT | 221178 |
rs540374083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073549 | CACACACAGGTGACA[A/T]TGGTGCCGGTGGCCA | 221178 |
rs540374282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067846 | AATAGCTGGGACTAC[A/G]GGTGCCTGCCATCAC | 221178 |
rs540384861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185799 | TGTGTGTGTGTGCGC[A/G]CACACATACATCAAG | 221178 |
rs540397861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096554 | CAGTGAGCCAAGATC[A/G]CACCACAGCCTGGGC | 221178 |
rs540403260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056241 | GGAATAGAACAAAGT[A/G]TCCAGAACAGCCTCA | 221178 |
rs540419665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140967 | ATCACCTGAGGTCAG[A/G]AGTTCGAGACCAGCT | 221178 |
rs540420823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247908 | CTTTGCCTCTACCAG[C/T]CACCATTTTGGTTTC | 221178 |
rs540430222 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283436 | ACTTGCACAGGAGGA[C/T]TGAGGCCATGAGTCT | 221178 |
rs540432920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034731 | CGGCACCTACACGTG[A/G]CTGCTTGTATGGCCT | 221178 |
rs540435770 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068282 | TCTGTTCCTGCTAGT[A/T]TGCTAAGGATAATGA | 221178 |
rs540439832 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24045956 | AACAATTAAAGTGAT[A/T]TGTGAGAAGGGATTA | 221178 |
rs540453239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102881 | TGCCAAAACCAACAT[C/T]GTGGAGACTTTTCCC | 221178 |
rs540474756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271321 | TGGTTTTTGCTTCTA[C/T]TACATGAAATTCCTT | 221178 |
rs540475773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233123 | TATGGTTTTTGTACT[G/T]CAGAGAATGTAAGTT | 221178 |
rs540486280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062438 | TTCTCCAATGGCGCC[A/G]GGGTGCACGGTGCTG | 221178 |
rs540489106 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986562 | CCAGGAGTCCCCTAG[A/C/T]GTCTCTAGGAAGCTG | 221178 |
rs540489341 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979607 | CACAGCCCCGGCCCT[A/G]GAAGCCGAGCTAGCC | 221178 |
rs540523450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008850 | AAAATGACTCACTGA[C/T]GGAATGACCCACAGG | 221178 |
rs540526018 | in-del | -/GA | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126547 | TATTTGTGTGTGTGT[-/GA]GAGAGAGAGACAGAC | 221178 |
rs540527626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090739 | TCCAGTGATTTGAAC[A/G]TATTTATAATAGCTG | 221178 |
rs540528021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980017 | ATCCTGTGCCCGTGG[A/G]ACATTTTTTTCCTGA | 221178 |
rs540539146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240384 | CTTGAGCCTAGAAAA[C/T]GGAACCCCCTTGAAC | 221178 |
rs540547028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167771 | TTGTTATAAACCATG[C/T]ATTTCTAAACATTAT | 221178 |
rs540553587 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282224 | TGGCACATGGCCAGT[G/T]CAGGTAAGATGAACT | 221178 |
rs540560221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009459 | GGTGGTTGGGCTACA[C/G]CCTAGTTTTATACAT | 221178 |
rs540576822 | in-del | -/CTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116507 | TTTCCTGAGCCCATG[-/CTTT]CTGCCTTGCACTCAT | 221178 |
rs540586210 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108417 | TGTTTATATTTTACA[A/G]TAAAGGCCTCTGTGA | 221178 |
rs540598651 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24130768 | CAGAAATCAACAGAA[C/T]CTGCAAACACGCTAT | 221178 |
rs540605057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119646 | AGAACAGCAGAGCCC[C/T]TTTGCAAGCTTTGTC | 221178 |
rs540609827 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24298853 | TTGGTCAGGCTAAAA[A/C/T]GGAAGCAGGGATCGA | 221178 |
rs540616976 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254759 | AGGCCCAGACTTCCT[A/G]TGGTTTAGCCCAGGC | 221178 |
rs540617620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252127 | TCCTGCATGTGGAGA[A/T]CCCTAAAGAACCGAG | 221178 |
rs540628897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291116 | GACACAAGGGCCATT[C/T]GTGAGCTGTGCCACG | 221178 |
rs540644941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003602 | CATCGTGTATTCAGT[A/T]CTTTTCGTATTATAT | 221178 |
rs540653349 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220918 | ATGGGGTCAGATTCT[G/T]CACTTGATAGGGATA | 221178 |
rs540656602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039404 | CTCCTTCCTAAGAGA[C/G]CACAAATATAGTGGA | 221178 |
rs540658363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257778 | AACTAAATCATAACC[A/G]CCTATCCACATTTTT | 221178 |
rs540663027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121706 | CATTTTAAATAGTCC[C/T]GTAGCCCTTGCCTAT | 221178 |
rs540669149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249952 | TCCCGTTCTCAAGGG[C/T]GGCACCATGTACTTA | 221178 |
rs540678781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998585 | ATTTTGATGAAATCC[A/G]GTTTGTCAGTTGTTT | 221178 |
rs540679654 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24278206 | TATTACAAGTAACAG[C/T]TACTGCTGGAGGAGA | 221178 |
rs540707360 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105458 | ACTTTTTTTTTTTTT[A/G]ACATATCAATTTCTT | 221178 |
rs540708535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220370 | TCATGCCTTCTCTTC[C/T]GTATTCAGTGCGAGT | 221178 |
rs540715840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299147 | TAGTCGTCATATGAC[A/G]TTGTCTAGCGCAGGC | 221178 |
rs540721668 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979698 | GAGCCTGTCTGAGTT[C/G]TGCTGGGCGGGGAGC | 221178 |
rs540753520 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304626 | ATCAAGAAAACATAA[A/C]CTTGGTCCTCAGGTG | 221178 |
rs540759486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992166 | GGGTTCTTGGTAGAA[A/G]GTGGAGAACTGCAGT | 221178 |
rs540759917 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998412 | CTTTTGTCCATTTTT[A/G]TCAGGTTGTTTTCAT | 221178 |
rs540764365 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295957 | CTGGCTTCAAAGTCC[A/G]TGCTGGTGATCACTG | 221178 |
rs540808902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994921 | CTGTAAACAGGTGAA[C/T]TGGTGTAGCTCAGCA | 221178 |
rs540817468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149005 | TGGGCTTGGAGGAAT[A/G]TAGGCTCCGTCCACA | 221178 |
rs540833245 | snp | A/C/G | 0.00239401 | 0.0345304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141420 | TGCTAATGCATTTGA[A/C/G]TCTTCTGCCTTTTCC | 221178 |
rs540845965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182834 | CAGTGTTAGAAAAAC[A/T]CAGCATGTTGCGCCA | 221178 |
rs540861893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191123 | AGTCTTTTTAAATTT[A/T]TTAATTAAATTAATT | 221178 |
rs540869465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198419 | CTATTTCAGGTACAC[A/G]TGTGTTTTGCTGGAT | 221178 |
rs540879516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021705 | ATACTCTGTGAAGGT[G/T]GTTGGAAAATCTTTT | 221178 |
rs540891492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989304 | GCATGCGCCTGTAGT[A/C]CCAGCTACTCAGGAG | 221178 |
rs540914502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022052 | TTTCTCTTTTCTTTC[C/T]TTTTTTTTTTTTTTC | 221178 |
rs540928191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983294 | CTTACTGCGTCTTCA[C/T]GTGGTCATCCTTCTA | 221178 |
rs540931039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097894 | AATTAAACATGAAAG[A/G]GACAGACAACCATGG | 221178 |
rs540952144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274502 | AAATTGTGCATCATG[A/T]TTTGACGTTGTCAGT | 221178 |
rs540952394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025137 | ATGTTTAATTCTCTT[C/T]CCTTCTTTATTATTT | 221178 |
rs540962069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057711 | TTGGAATTGCCACAC[C/T]GTATATATGTGTGAT | 221178 |
rs540968913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157580 | GCTGGGATTACAGGC[A/G]TGAGCCACGTGCCCG | 221178 |
rs540977721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211526 | CTATGATTTTTAGCC[C/T]TGATTTTGTTGAGGA | 221178 |
rs540980398 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081324 | CCCTTCTCTTATTTT[A/T]TTTTATTTTATTATC | 221178 |
rs541009644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059952 | ATGCTTCCAGCTTTT[G/T]TCTTTTCAGTATTAT | 221178 |
rs541021131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070279 | AGAAATGTCCGAGGA[A/G]ATTAGCCCTGATGCG | 221178 |
rs541021206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255798 | TTTATATACCAACGA[A/C]GTGCTAGAATGGCAT | 221178 |
rs541030425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157338 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 221178 |
rs541030557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012930 | CTGGGGACAGGGCAC[A/G]CCTAGGCCACAACTC | 221178 |
rs541032079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018972 | ATGCAGAAGAATACT[A/G]AGGCATATCTGATTG | 221178 |
rs541037707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000723 | TTAGAGGTGTGAATT[C/T]GGGAGAGCTCTGGGT | 221178 |
rs541043344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005869 | ATAGCTGACATTTTT[C/T]TCCCTTCTTAATAAA | 221178 |
rs541063037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095305 | CACTAAGTGAAATAA[A/G]CCAGTCACAAAAGGA | 221178 |
rs541063272 | in-del | -/TTTG | 0.0539704 | 0.155153 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058967 | GTCTGTGTATTGTTT[-/TTTG]TTTTGTTTTGTTTTG | 221178 |
rs541070766 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24183735 | CCCTGCTTTATAATG[A/T]TCTCTATGGGCTAAT | 221178 |
rs541079576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242542 | GTGTCTTAACTATCT[C/T]GCTTGCTCTTATCTT | 221178 |
rs541098046 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249121 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAGAGTGC | 221178 |
rs541104077 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186330 | AATTGGATGCTACAC[C/T]AGCAATTAGGGATTA | 221178 |
rs541104396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217318 | TCTCTCTTTTTATTA[C/T]AATTCTTCTTCCTAA | 221178 |
rs541111457 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015869 | AAAATGAAGTTGTTG[A/G]TTCTTAGAAATAATT | 221178 |
rs541120088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006669 | CTTAGGGGCCTGCAC[A/G]GCTATGGTCCCATTT | 221178 |
rs541132150 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128150 | CTTTATTCGGAGGAA[G/T]AAAGCACCTTCTACA | 221178 |
rs541132324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163513 | TATGGTCTCTGTTAG[C/G]TGTGTGACTGTATGA | 221178 |
rs541137616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111309 | CTCCGTTGCTAGTAC[C/G]TTAATTCAGATACTC | 221178 |
rs541143588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116571 | AGTCCCCACAACGAC[A/T]GTATCTAGGAGTTCA | 221178 |
rs541151740 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037156 | CAGGTTCTTCAATGA[C/G]AACACTTGGACACAG | 221178 |
rs541154414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203900 | GTGCCAGACACTGTA[C/T]TGTGTGTATATGCTG | 221178 |
rs541157471 | in-del | -/AAAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24107261 | AAAAAAAAAAAAAAA[-/AAAA]GCTCAAGCCTGGTTC | 221178 |
rs541161685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302112 | GATTCTGCCACTTCC[C/T]GCTGCACGTCCTGGC | 221178 |
rs541170228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143248 | GCAGGAAGTCTAGAC[A/G]GAAGCCCCTGGTGTT | 221178 |
rs541188394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037608 | AGAGATGGAGTTTCA[C/T]CATGTTGGCCACGGT | 221178 |
rs541195570 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23997877 | AACACTTCCCACTAG[A/G]CCCCATCTCCAACAC | 221178 |
rs541196018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122498 | ATTCTTGCCCATCTT[C/T]ATCAATATCATCTTC | 221178 |
rs541196179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169799 | GCTTCCAGAGGTTTC[A/G]GGTGGCTCAGTGAGT | 221178 |
rs541196781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189007 | ACCTACTGTTTAGAA[A/G]AAGGATTCTTTTTGA | 221178 |
rs541198875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995564 | CCATATCGACTGAGG[C/T]TTTCCCTTTGAGATA | 221178 |
rs541206549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111702 | TGAGCCGCCATGCCC[A/G]GCCTGCGTCCATATT | 221178 |
rs541212049 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275846 | GTCTTAGGCAGGAGA[A/G]TCTCTGGAACCCTGG | 221178 |
rs541226425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230878 | TGGTGGAAAGTCAGT[A/G]ACATTGTCAGGGCAG | 221178 |
rs541233410 | snp | A/G | 9.71865e-05 | 0.00697021 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223052 | GAAAGACGCCAAGAT[A/G]GTGACCTCCCTTGCG | 221178 |
rs541262182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042795 | CCCAAGAATCTGCAT[C/G]TTACCAAGCTCTCCC | 221178 |
rs541266887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022251 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCTGAC | 221178 |
rs541267107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024490 | CACATGCAAGAAGAA[A/G]GGAGAGTGCTATCTG | 221178 |
rs541272622 | snp | C/T | 5.02534e-05 | 0.0050124 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294905 | TGATCCCATGCCACT[C/T]GCCCTTCCCGCACCT | 221178 |
rs541276125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031287 | GACCAAGGTCTGGTC[C/T]ATAGCATAACTGGTT | 221178 |
rs541281981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002526 | AGGGAAACACCAGAT[C/T]GGCCTCAGTGGCCTG | 221178 |
rs541284661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002000 | AAGTCACCCAGGGGG[C/T]GGGTGGGAGCAGAGG | 221178 |
rs541305814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139360 | ACTCCAGCTTACCTC[A/G]TAGTGGGGGCACTGT | 221178 |
rs541323734 | snp | A/G | 0.000560905 | 0.0167373 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223265 | CTTCCGGAAAATGGG[A/G]TCCTTTAAGAAACTG | 221178 |
rs541347922 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032284 | TGCTGTATTCAACAC[C/T]GAGCCTGCTCTCTCT | 221178 |
rs541357892 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24169181 | TTCCTAGAAAAGGCT[C/T]GGGCTCTTTACTCGG | 221178 |
rs541359429 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306905 | CTGAACTGAGGAATT[C/T]GCTGTTGACAGCCAA | 221178 |
rs541371404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133829 | AAGGGGCAAGGGGAC[A/G]GGGCAAACAATCATC | 221178 |
rs541377154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139735 | CTACATGATGTAGAA[C/T]GATCTGCTTAATTGA | 221178 |
rs541412799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042420 | CTTTCTGAGATGTTG[C/T]GTGTTCACAGTGCTT | 221178 |
rs541419304 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019349 | CGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 221178 |
rs541419530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164180 | TGGAGAGAAATGCAT[G/T]GGTACAAAGTGCTTA | 221178 |
rs541431004 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154539 | AACGGGGGGGAGGGG[C/G]ACATAAGGGAGTCTT | 221178 |
rs541440483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134182 | TGTGGGTTTGGGCCA[A/G]TGAATTTCTCTCCCC | 221178 |
rs541445257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149140 | GCGTCCTGTCTGCCC[C/T]CTGCCTGTTGCCATC | 221178 |
rs541450932 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054184 | GCCACTTCCAAGGCC[A/G]GAAGCCCGGAGTTCC | 221178 |
rs541452184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088434 | TTCCTCTTGAGATGA[A/G]GACACATGAGAACCC | 221178 |
rs541466772 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160728 | CTTGGCTGAGTGTGC[C/T]GCCGCGGCGCGGGAG | 221178 |
rs541475837 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239644 | AGGCTGCAGTGAGCC[A/G]AGATTTCGTCACTGC | 221178 |
rs541479708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284940 | TGGCTGGCGAATGGC[A/G]GAGCTGGAGGCACCC | 221178 |
rs541485430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037660 | TGATCCACCTGCCTC[A/G]GCCTTCCAAAGAGCT | 221178 |
rs541487416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201543 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 221178 |
rs541504950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210196 | GTCCTTTACTTGTTA[C/T]ATGACTTGCACATGT | 221178 |
rs541506905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149693 | GCTGATGGGGGCGGG[A/G]AAGCTCCCACCCATG | 221178 |
rs541508372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047681 | CTTTATCATTATCAA[C/T]CCTTAGTATTTTATC | 221178 |
rs541511792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246812 | AGGTTGCGGTGAGCC[A/G]AGATCACACCACTGC | 221178 |
rs541542251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231781 | GTATTGTCAGTATTC[C/T]GGACTCTAGCTATTC | 221178 |
rs541550421 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207811 | CAGGGAGGCAGTCGC[A/G]GTGGATTAGGAACAC | 221178 |
rs541557439 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24048301 | CATTTTTAGCATTAC[A/G]TTATATTGTTTAGAA | 221178 |
rs541602392 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24236527 | CTTGAACCCAGGCGG[C/T]GGAGGTTGCAGTGAG | 221178 |
rs541604853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983393 | CCTCATTATACCTCA[A/G]TTACCGCTATGAAGG | 221178 |
rs541644025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043037 | GCCAGTATTGGCTCA[G/T]TTGAGTGGAACACAC | 221178 |
rs541646560 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271587 | AAGAAACTTTGTACT[C/T]TCACACTAGGAAGCC | 221178 |
rs541687324 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23983903 | GTGCAGATGGCAAAG[C/T]GTAGGCCTCACAAAC | 221178 |
rs541689126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100985 | TTTCATGTGACTGAC[A/G]GTAGCACAGCATTAT | 221178 |
rs541692335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077910 | CCTTGGTTGGTCCCA[C/T]ATCCTTCTCTCTTGC | 221178 |
rs541695923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219719 | CATTCATTGCAGGGG[G/T]CTCAGGAAGGAATTC | 221178 |
rs541703339 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24302262 | AGCTACTGGACCTTC[-/T]TTTTGGTTAACGTGA | 221178 |
rs541723016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187700 | TAATTGTTTTGGGCT[C/T]CATGAACTACACCTA | 221178 |
rs541728145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134212 | CAGCATGAGGACTTC[A/G]CTGCCTTTATGCAGG | 221178 |
rs541729646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071234 | TGAGCCCTAGGACTC[A/G]TAGTAGACACATTGG | 221178 |
rs541733015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038134 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 221178 |
rs541735102 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259151 | AAGTGACCCTGCAGG[A/G]ATGCTGCTACCTCCT | 221178 |
rs541750217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095364 | AGTACTTAGAGTAGT[A/C]AAAATCATAGAGATA | 221178 |
rs541760022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181080 | GGTACAGAAAAATAC[A/G]GTATAAAAGTTTTTT | 221178 |
rs541765265 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219206 | AGTTAATTGAGGTCA[A/C]ATTATTAGTTCTAAA | 221178 |
rs541770156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266582 | AGCCACCACACACAA[A/T]CTTCAGTGTTTATTT | 221178 |
rs541771645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076101 | AAACAGAGAAAAGAG[A/G]ACTTTGAAATTCATT | 221178 |
rs541781168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185015 | GTGGGCACTGGGGCC[A/G]TCTTTGAAAGGCACG | 221178 |
rs541792682 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24124695 | TTGTATAGATACTGC[G/T]TTTGTCTGTTGTAAT | 221178 |
rs541792727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071670 | CCCTGCATTGAATCA[C/T]ATCAGATTTAATGTT | 221178 |
rs541793200 | snp | C/T | 0.000592885 | 0.0172073 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24297596 | GGACTGCAACCTCAG[C/T]GTGAAAAATGCCTTC | 221178 |
rs541797176 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225756 | CCCCAGAAGGGTTGC[A/C]ACTCTTCACGCCTGC | 221178 |
rs541798322 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037221 | GGTGGGGGGAGGGGG[C/G]AGGGATGGCATTAGG | 221178 |
rs541799303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054359 | ATTAGCTCTGTCCAA[A/G]TATCCAAGTGGGAGA | 221178 |
rs541807233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082455 | GAGTTGCTCTTTGGA[G/T]AGTTTTGTCCACCAC | 221178 |
rs541812244 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977893 | TTTTTTCTTTTTCTT[G/T]TCTTTTTTATTTATT | 221178 |
rs541826218 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24295625 | TCAAAAAAAAAAGGA[A/G]AGACCACAAATACAA | 221178 |
rs541834969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083299 | CCAGCTCTTGCCACC[A/T]GACAAAGGGCACAGA | 221178 |
rs541844447 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24017509 | TGTTTGTATGTGTAT[A/G]TATGTATATGTAAGA | 221178 |
rs541877903 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160163 | CCAGGCAGTGGGCAG[C/T]GGGGCACGGTTGCCC | 221178 |
rs541890741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282403 | GCACCATCCCAGGGC[A/G]ACCTTCAGCCAGCCC | 221178 |
rs541892887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111774 | TGAAACCATCCTTGC[A/G]TTTCCTACTTGGTCA | 221178 |
rs541898319 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083867 | CACTGGGGGAAAAAA[A/C]CCCCGTCTGGAGATG | 221178 |
rs541900387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200702 | CTCTCGGTGGTCCCC[C/T]TAAATTACACGTGTG | 221178 |
rs541907934 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23998362 | TTGTTCTTATTTTCC[A/G]TCTTTATCTTCTTTC | 221178 |
rs541926731 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275913 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACCTT | 221178 |
rs541927494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281915 | TGCATGAGCTTGAAC[C/T]CCTCCTCATCATGAC | 221178 |
rs541930394 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23991048 | GCTCAAGGTTAAGAT[A/C]AGGCAGAGGAGAAAC | 221178 |
rs541930917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195647 | ATAAGACTCTTAATT[A/C]TTTAGGCATTGATTA | 221178 |
rs541937348 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24072062 | AGAAGTGCACATGTC[C/T]AATCAAGAATATTAA | 221178 |
rs541949375 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079591 | AAATGCTAGTAATAC[-/A]GGGGGGTCCTGACGG | 221178 |
rs541954136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112172 | TGCACTTCTGCCCCC[A/C]ATTCCTTCTTGCAAA | 221178 |
rs541955642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139450 | CAAAAACCCACACCA[A/G]TTCTCCTCTGGGATT | 221178 |
rs541955851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071124 | AGGAACTAGGGATGC[A/G]TAGAAAACTAGTGCT | 221178 |
rs541957972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031858 | CAAGATATTCTGTGT[A/G]CCATATTTACAAGCT | 221178 |
rs541963674 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24165812 | AGTGTTAATGCGACA[A/G]TTCAGTCTCATTACA | 221178 |
rs541971011 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189544 | TACATATTTATATTT[A/C]AATATATAGTATATT | 221178 |
rs541974275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100519 | AGCACATGTGGCCTT[C/T]TTCCTTCATCTTGTA | 221178 |
rs541974968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167139 | TTGGGAACCACTGTC[A/G]TAGGTGAGGATTCCA | 221178 |
rs541981512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118260 | CCCATCATGGTCTCT[G/T]TTTACCAACAGGGGT | 221178 |
rs541983600 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231355 | TGGAATCCTGTAATA[C/T]GTGGTCTTTTGTGAC | 221178 |
rs541983688 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23980007 | TTTGGCCGAAATCCT[G/T]TGCCCGTGGAACATT | 221178 |
rs541990410 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303461 | GTGCAGAGCAACTTA[C/T]GCATCCTCAAGAATC | 221178 |
rs541997404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025350 | CCAAAAAATATATAT[A/G]ATAATAATACATGTG | 221178 |
rs542000459 | snp | A/G | | | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252918 | CCCAGGAGCTAGTGA[A/G]GTATCCAGTGAGCAC | 221178 |
rs542011990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275947 | CCTCACCCCTCCCCC[A/C]AAAAATGTTTTTTCC | 221178 |
rs542013341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287364 | GATAGGGTCTCACTG[C/T]GTTGCCGAGGCTGGT | 221178 |
rs542036273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172861 | TCTCCATCAACATAA[A/C]ATCTTGCTGGGATCT | 221178 |
rs542039286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997254 | ATTGAAAGTGTACAC[C/T]GTGGTACATATGTGT | 221178 |
rs542056345 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24146858 | CCACCGCATCCGTCC[C/T]CGCCCCACCCCTCCC | 221178 |
rs542059503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280880 | GCTCTCCGACTGTAC[G/T]CACCCTGGCCTAGCA | 221178 |
rs542061665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286589 | CTCGGTGTTTCTCTG[C/T]GGTCCTCGTGCCTGC | 221178 |
rs542074093 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24229067 | GAACAAGTACTTAAG[C/T]TTGTGACCTGTTTTA | 221178 |
rs542098425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286130 | AGGATACCAGTGTCA[C/T]CCTGAGAGAGTGCAC | 221178 |
rs542105380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172223 | GAATGTTTGGGATTG[A/G]CTTTTTTCACTCAGT | 221178 |
rs542131974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019437 | GTTTTATACTGTATG[G/T]TTTGATAGCAGTGGA | 221178 |
rs542134449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026768 | ATTTTTAGTGGAGAC[A/G]GGTTTTCACCGTGTT | 221178 |
rs542146347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256758 | GGGACAGGCCTGAGT[C/T]ATGTTTGTAGGCTAC | 221178 |
rs542146642 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263776 | CCACAGATACGGAGG[A/G]CCAACTGTGTTTACT | 221178 |
rs542188579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164987 | CAACACCGCAGAATG[C/T]AAGGAGAATGGCGTC | 221178 |
rs542192786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184576 | TTGTTGATTTTTTTT[A/C]TCTCTGATGTGTAAT | 221178 |
rs542204428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984891 | AATGCAAGTCCCTGC[A/G]AGGTAGAATGGTCTG | 221178 |
rs542204547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140502 | ATTCTGGAACCCCAA[A/C]CACAAGGGTCACGTG | 221178 |
rs542207316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225152 | CCAGCAGGCTGCATT[C/T]GGCTTGCACTGCCAG | 221178 |
rs542219605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048602 | AATTTCTAAAATTCA[C/G]TTAGGTTCTTGATGA | 221178 |
rs542220164 | in-del | -/TGGGTTTTTTTTTTTTGTTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24104236 | AATGTAAAGCTAGAA[-/TGGGTTTTTTTTTTTTGTTTTT]TGGGTTTTTTTGGAA | 221178 |
rs542229510 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24037659 | GTGATCCACCTGCCT[C/T]GGCCTTCCAAAGAGC | 221178 |
rs542231063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098409 | AATTAAGACTTAAAC[A/G]TGGCAAAACCCTGTC | 221178 |
rs542237415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058237 | GGAAGGAAGGATTCT[A/G]GTGTTGAAAACTCTC | 221178 |
rs542244055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128658 | AGGCCTTGTTGTGGA[A/G]ACAGGACTCCCGGGA | 221178 |
rs542245221 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989830 | ATGAACAGGGTTGGT[A/G]CCCTCAGAAAAGAGG | 221178 |
rs542258081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016888 | GGATGGCGCTGCCCC[C/T]GCCCAGGCTCATGCC | 221178 |
rs542273466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231917 | GATTTAGTGAAGTGC[C/T]GATTCAGATCTTTTG | 221178 |
rs542284167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266707 | CAGTGTTGCCAATAA[A/T]CAATGATGGTCATTT | 221178 |
rs542293952 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143849 | TGGAGGAACATGTGA[C/T]ACTTTCTCTCTGGCC | 221178 |
rs542295265 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305168 | AATATTTATTCATGG[A/G]TAATGAAGAAATGGT | 221178 |
rs542305258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122756 | GCCATCTTGCTGGAA[A/G]ACTTCAAATACAAGG | 221178 |
rs542305743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004294 | CAGGAGTGAAATCCC[A/G]GTTCTTGTACCAACA | 221178 |
rs542321818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154090 | GTAGAACTCTCTTCT[A/G]CCACTTGTGGGAGTG | 221178 |
rs542322149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187315 | GAAACTACGCTTCTG[A/G]TTGTCTGGCCTCTTT | 221178 |
rs542324860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276569 | AAAAGTTCTGTCGTA[C/T]AAGAGTGTGAATATA | 221178 |
rs542342032 | in-del | -/TGT | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123051 | AATGTCATTGCCAAA[-/TGT]TGTGTCATTTCTACT | 221178 |
rs542347957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011079 | TTGCTGACTCCTCTG[A/C]AACCTTGGCTTTGGT | 221178 |
rs542354251 | in-del | -/CA | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120577 | GGTGAGCCACTATAC[-/CA]CCCTCTGCCTCTGTT | 221178 |
rs542368217 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23994404 | GCTTCAGAGAGCACA[A/G]TGAGGGTGGAAGCTG | 221178 |
rs542384923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153573 | TTCAACAGAGGACAC[A/G]TGGTAGAGAGAATGA | 221178 |
rs542397430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150284 | ACCGCATGTCCTCAG[C/T]GCTCTCAAGTGGCAT | 221178 |
rs542412741 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158790 | AGTGAGGTCCCACTG[A/T]CACCGGCTCACTGAC | 221178 |
rs542432185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237643 | AGTGTGAATGTACTT[A/T]ATCCCACTGACTCAT | 221178 |
rs542435031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240026 | ATTGCAACCTACGAC[C/T]GGGTGTGGTGGCTCA | 221178 |
rs542436060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038192 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC | 221178 |
rs542448326 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089445 | TGGTCTATTATTGTC[C/T]TTTAGTAGGCAGAAG | 221178 |
rs542452837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278380 | CGGTTCATCTCCACA[C/G]CTTAAATCAGTGCCT | 221178 |
rs542455600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113369 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 221178 |
rs542456864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109839 | TTGCATGAATAATAT[C/T]ACCTGTGCCCATCAC | 221178 |
rs542457180 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115559 | TGGAACAGTTTCATC[C/G]CCAAACCATCTCTCT | 221178 |
rs542459489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201514 | GGTGCAATCTTGACT[C/T]ACTGCAACCTCCGCC | 221178 |
rs542460846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151069 | TGCGAAGATTCATAA[A/T]CCTCATAATTTTACA | 221178 |
rs542467066 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038690 | GTGAGTTGGCCCCTC[G/T]CATCCAAACAACTCT | 221178 |
rs542469018 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276919 | GCTGGCATTGACACG[C/T]TGTGGACTACTACAT | 221178 |
rs542482451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081214 | AGATCTGTCCAAGTC[A/G]TGCATGAGAGACCAC | 221178 |
rs542483653 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185932 | GGCGTTGATGTTTTA[A/G]GCTTGAATCTTATGG | 221178 |
rs542490854 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198048 | TCGCCCAGGCTGGAG[A/T]GCAGTGGCATGATCT | 221178 |
rs542493461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244909 | GTTAAAAGGGCAGCA[A/G]TTCCACTGAAAAGTC | 221178 |
rs542505196 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082424 | ACACTGATGGAGAAT[G/T]CACCTTGAGATGATT | 221178 |
rs542518509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110516 | TTCACTTGAATCTGC[A/C]TCAGCCCCCAGTCTA | 221178 |
rs542527567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162961 | GAGGACATGAATTCT[A/C]TACCTGTAGGACAGT | 221178 |
rs542546861 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24086263 | ATCATTCATATTGCA[C/T]GGTACATAGTCTTGC | 221178 |
rs542551704 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064241 | ACAGACAACAAAGCT[A/G]CTAGAATGGCTACAG | 221178 |
rs542573954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016340 | TGTTTCCCAGTAGCT[A/G]CCATTTCCATTTGGA | 221178 |
rs542586258 | in-del | -/TCTTCC | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142673 | CCTCTTCCTCATCCT[-/TCTTCC]TCTTCCTCTTCCTCT | 221178 |
rs542593322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248002 | TAGTCTGCCTTCTCT[A/G]GTGGTTCTGGTTGTC | 221178 |
rs542594252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067164 | CTCAGCCCAGGCACT[A/G]CTGCCTGCCCAATCT | 221178 |
rs542595652 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24078529 | CTGACATAATGTGAC[-/T]TTTAAGTATGCTCAC | 221178 |
rs542597065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267601 | TTGCTTTTTGAAAAC[C/T]AATGATTTTAACCAA | 221178 |
rs542599565 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993982 | GGTGTTTTTTTTTTT[C/T]TTTCTTTTTTTTTTT | 221178 |
rs542608717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168404 | TAGATTATGTTTTTG[A/G]TTTTGTTTTGCCCTG | 221178 |
rs542608778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174460 | TCTTATATGAGCATT[C/T]CGTGCTATCAGTTTC | 221178 |
rs542609218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010276 | ACAGTGGGGCAGAGG[A/G]AGCAATCAGATATGC | 221178 |
rs542618343 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24158195 | CAGTTAGAGTCTTGA[C/G]TACCAAAAGATCAGC | 221178 |
rs542624967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051245 | GACCTTCCAAGAGGA[C/G]ATGAACAGCAGGAAG | 221178 |
rs542625994 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139984 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 221178 |
rs542635722 | in-del | -/AAA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128749 | TTAAAAAAAAAAAAA[-/AAA]CTGCTTACTTCCCTT | 221178 |
rs542640865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131276 | GTATGGGCATATCTT[G/T]TCTTGACCAGCTAGT | 221178 |
rs542643429 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104780 | AATAACTTGTTAGTT[A/G]ATGTTTTAAACTCTG | 221178 |
rs542649857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023958 | GCATGTGGACGCTAA[C/T]ATCATAGTCAGTTCA | 221178 |
rs542665305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294287 | CTCCTGTCCTTTCCC[A/G]AACAGCATAAAAGAT | 221178 |
rs542666496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125513 | CAGGGGTCGTATGGA[C/T]CAACCTAAACCACCC | 221178 |
rs542676168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258758 | TCTTAGTGATAAATC[C/T]AGCATGCTACATTTC | 221178 |
rs542682255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132318 | GAACCTCTATTCAGT[C/T]GAGCCATCATGCTCA | 221178 |
rs542688474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024385 | GATGGATGGATGGAT[A/G]GATGGAATGAAGGAA | 221178 |
rs542704079 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290345 | ACGTTAGAGGCCCTG[C/T]TCCCCACCTTCCAGG | 221178 |
rs542713049 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24258251 | AAAAAAAAAAAAATA[A/G]AAAGAACTCTGGATT | 221178 |
rs542717707 | in-del | -/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24014798 | CAAGTTATTTCAGTT[-/C]CTGTCTTCTCCCTTT | 221178 |
rs542725931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120693 | AAAGTAATGCTCCAT[A/C]AAGGGTTGTTGTTAT | 221178 |
rs542728664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138521 | TTCTTTAATAATTAG[A/C]AAATATCCTTTTCTT | 221178 |
rs542732994 | in-del | -/A | 0.213937 | 0.247385 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140069 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 221178 |
rs542750036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132883 | GTATGATGAGGGCAC[A/G]AGAATCACTTGAACC | 221178 |
rs542750504 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157101 | TCTAGACCTTAAGTT[A/C]CTTCCTCCAGGTGAA | 221178 |
rs542754566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228733 | TTCAGCTCATTAACA[A/G]TAAGGTTCTACTTAC | 221178 |
rs542758451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273319 | CAGGGCCCTAAGTTG[A/T]ATACTGATGTGAAGC | 221178 |
rs542763118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099613 | GGGGAGGGCCCACAG[C/T]CCCCCGGGTGGTGTT | 221178 |
rs542763739 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24247945 | AGGGAGCCGGTGGGC[C/T]GCGGCACAAGCTCTG | 221178 |
rs542795865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059218 | CCTCGTAATCCACCC[C/G]CCTCGGCCTCCTAAA | 221178 |
rs542799217 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029742 | TAAAGCCTGGTACCC[A/G]TTAGTTAATTTTTTG | 221178 |
rs542803039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265263 | AGTCGGCCTGCTGAG[A/G]CAGCATCTACCCGGC | 221178 |
rs542807203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126840 | GATTTGGTTACAGGC[A/T]TGAGCCACTGCACTC | 221178 |
rs542816448 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018163 | TTTTGGGTTTTGTAT[C/G]TTTGTTACTGGATGA | 221178 |
rs542831372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242204 | GCCTAGGCAAGGAGA[A/G]AGAGAGGAAGAGAAC | 221178 |
rs542832789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053260 | TCAGAGCTAGGATTC[C/G]GCCTCAGTGCTGTGA | 221178 |
rs542853321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227500 | TTTATTAAAGGTGCG[G/T]GCACATGTTGATAAT | 221178 |
rs542853368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012398 | GCTCGTGGTTGGTCA[A/G]TATCTTGAGAAGTAC | 221178 |
rs542862812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993562 | TGCCAAGGACGTTCT[C/T]GGCCCAGCACCTGAT | 221178 |
rs542870390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127464 | GGGTAGGGGAGCCCC[C/T]GTAGGTAGTCTACTG | 221178 |
rs542929106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069144 | TTTAAAATATTTTTT[A/T]CTAGTTCCATGAAAA | 221178 |
rs542930371 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24207478 | CATGTAATAGTTCTG[C/T]GTTTGAGTTTTTGGG | 221178 |
rs542933087 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139348 | ACAGAGATTGAGACT[C/G]CAGCTTACCTCGTAG | 221178 |
rs542936121 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029105 | TTTTAATAGTTTTTG[A/T]TAGTAACGGGGTCTC | 221178 |
rs542938974 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24032970 | TGTCTCACTCATTTT[A/G]GGTAGATTGGAAAGG | 221178 |
rs542962821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202389 | GTGGTGCCCACAGTC[A/G]TAAAGGACAGTTGAT | 221178 |
rs542969008 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274547 | TCTTTCCCTCTGTGT[A/G]CATCTCCGTGGCCTG | 221178 |
rs542971498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122109 | AATTGAAAGAACTTG[G/T]CACAACTGGAGCACT | 221178 |
rs542995998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158098 | AGTGAGAGGTGGTAG[C/T]TTCTATCCTTAGACA | 221178 |
rs543020599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199666 | ATGGGAAAAACTTGC[A/G]TCTTGTGATCTAAGC | 221178 |
rs543032001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080657 | GAGATTTCATCGGTG[A/G]CCTTGATGTCACAGA | 221178 |
rs543036373 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24218417 | TCCACCCTGCTGGGC[C/T]GTCACTACAGCAATG | 221178 |
rs543036757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099044 | GAGCTATGATCATAC[C/T]GCTTCACTCCTGCCT | 221178 |
rs543045237 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171898 | ATAATTGTATCAGCA[A/G/T]ATACCTCAAAATTCT | 221178 |
rs543058209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064081 | GACCATGCCTGCCTA[C/T]CCTTCCAGCACTTTC | 221178 |
rs543061406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011506 | CCTGGAATTCTGTTG[C/T]CACGCTCCCTGTCCT | 221178 |
rs543061916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214794 | GTAACATAACCTTGT[C/G]TCATCTTGCATCTCC | 221178 |
rs543096977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064748 | AAAATGCTGCTGGGT[A/G]CCTTCTTAATCAGCG | 221178 |
rs543106065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293964 | TTGCCACGGGAAAGC[A/G]GAAAATATAGCTCAT | 221178 |
rs543115007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046390 | CTCTGACTCCTGGGG[C/T]TCAAATGATCCTCCT | 221178 |
rs543117996 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255877 | CATCATTTTGAGACA[A/C]GTTGGGGAGATTTTC | 221178 |
rs543124834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214224 | CTGCACATGTGGTAC[A/T]TCTTCTGCACCTCCA | 221178 |
rs543145492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982606 | GTGAAATGCTAGGGA[A/G]TACCTATTTCATAGG | 221178 |
rs543146760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052603 | CCAGATGAAAGCCAG[A/G]CTGTGGATACTGGCC | 221178 |
rs543150238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081866 | CCTTTCACTTTCCAC[A/G]CCCACAGACAATGCT | 221178 |
rs543150610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005256 | AAAACTGTTTTGATT[C/T]TTAAATTTTTACCGT | 221178 |
rs543152511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291663 | GACTAAGCTCTTCTT[A/G]TTACTCACACTTCTG | 221178 |
rs543157483 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212222 | GTTCAGGGCTGTGGG[A/G]AGCTGTGATTGGGCC | 221178 |
rs543180652 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044591 | ACAGTGTGATGTTTC[A/G]ATACATGTTTACATT | 221178 |
rs543192988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179398 | ACATTTCCATCAGCT[A/G]TGTATGGGGGCTCCA | 221178 |
rs543211101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220452 | TTTTGATTAAACAAT[C/T]TCATTCATTTCATGA | 221178 |
rs543214497 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093724 | TTATTTTAATGTTAC[A/G]ATTTTATGAAAAGCT | 221178 |
rs543227933 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269433 | GACAGGATCTAGCTC[-/TG]TAACTCACAACACTG | 221178 |
rs543252585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104403 | TTTGGTTTTACAATT[C/T]TCAAGGCAGGCATAA | 221178 |
rs543253577 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24186077 | CTGTCAATCACATCT[A/C]GAAAAGATCTTCACA | 221178 |
rs543269904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148239 | TATGTCTTTTGATTA[C/T]GATCGTTACTATTGT | 221178 |
rs543272380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217424 | CCCAGATGTTGGGGT[A/G]TCAGACCTGAGATGT | 221178 |
rs543299060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231249 | CCAGAAAGAAGCCTC[A/G]CGCCATTTGCAGTCA | 221178 |
rs543306196 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304698 | GCCACCTTGGCACAC[A/G]TGCTTACAGGCAGCA | 221178 |
rs543332887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005942 | CCGTACTGTTTCTTG[A/C]ATAATCATCACCTGT | 221178 |
rs543337605 | snp | A/G | 0.00143228 | 0.0267224 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223694 | GAGGAGCAAGAGCAC[A/G]GACAATCTTGCCTTT | 221178 |
rs543339192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088161 | ACTGTCATATGAAAA[C/T]TTGGGCTGAGGTGTG | 221178 |
rs543360368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230913 | TCAGAGGGACATTCC[A/G]TGGCTGGGGTTGATC | 221178 |
rs543369711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286644 | GCCATGAGACTCAGG[C/T]GAGGGCCAGGCTGCC | 221178 |
rs543370100 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268724 | AGATCGTGCCACTGC[A/T]CTCCAGCCTGAGTGA | 221178 |
rs543370319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030524 | CTTTTCCCTAATCTC[C/T]TGCCCACCCATGTTT | 221178 |
rs543371056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006563 | AGAGGCCAGGCCAGG[A/C]CGGCCCAAGTACTAA | 221178 |
rs543376008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011103 | CTTTGGTTTCTCCCC[A/G]GGTCCTGACCACCTG | 221178 |
rs543396705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988767 | GTTTCAGGGACATTG[C/T]ATTTCTTTTACTGCA | 221178 |
rs543397987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206752 | CAAAAATTAGCCAGA[C/T]GTGTTGGGATGTGCC | 221178 |
rs543407214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024438 | AAGAAGAAGAAACAC[C/T]CCTCATTCTCTTGGG | 221178 |
rs543414356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017328 | TGGACCCGAACCAGA[A/G]CCTACGTAAGCCCAC | 221178 |
rs543430692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120796 | CTGCCAGGTGTTTTC[A/T]TTGCCTACCAGGTAC | 221178 |
rs543437520 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982773 | GAACGAGTCAGACAG[C/G]GTCACCCAGAAAGGA | 221178 |
rs543438953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126262 | TTGAGTCTGGGGGAG[A/G]GGTAGCTGGAGGTGG | 221178 |
rs543459146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211916 | AGAGCATCCGTGTGT[C/T]GGCTGAAGGAGGCCA | 221178 |
rs543481504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124528 | TGGTGGGACGCAGTG[C/T]TCTCATCTAGATTCT | 221178 |
rs543518980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133747 | AACCAGAGCACAGGG[C/G]AGGAGAGGCAGAATA | 221178 |
rs543524381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177506 | TTTTTATTTTTTTAG[A/T]CACAGTCTTACTCTG | 221178 |
rs543528522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115618 | CTACAAAACCAGTCC[A/G]TGGTGCCAAAAAGGT | 221178 |
rs543543121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075185 | CAGCACTATTTTAAA[C/T]CTGTATGTAGCTACT | 221178 |
rs543545341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198458 | AAGGTGAAAAAGAGT[C/G]TAGAGGTCTCCAAAA | 221178 |
rs543546056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041553 | GGTCAAAGGTTAAAC[G/T]ATGTTGGAAGCACAG | 221178 |
rs543562030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053785 | GAATTTTAAGACACC[A/G]AAACAACCCCTTAGT | 221178 |
rs543563287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24218386 | AGGTAGCAGTGCTGG[G/T]GTGGACCCTCTGATT | 221178 |
rs543564634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121676 | CTACCTTTGAGTTTT[A/G]TACTGCAAATGAGAC | 221178 |
rs543580069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127496 | GAACAGCCTCTGGGG[A/T]CAGCAGCTGGAGAAG | 221178 |
rs543581303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012854 | TTTATGCGTCTGCAG[G/T]TCGGGGCTTTCACGG | 221178 |
rs543585915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183953 | CTTCCCACACACAGC[A/G]CATTGAGCAGACATT | 221178 |
rs543599763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122171 | TTGGATTCATGGGCT[G/T]CTCTTCTTTGATCAG | 221178 |
rs543606270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069776 | TATTCTGTTATTCAT[A/G]TAATATTACCAGTTC | 221178 |
rs543608796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204428 | TTTTTTTAAATTTTA[C/G]TAAAATAGGTATAAC | 221178 |
rs543625553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210265 | TTTTGCTATGAAAAG[C/G]CTTTTAGCTTGATAC | 221178 |
rs543631055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249217 | CTCATCATTGGTCAC[C/T]AAACCACTATTTCAA | 221178 |
rs543634206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269246 | CCTAGAGACTTGGAA[A/G]CTTTCCCTAATTTTG | 221178 |
rs543642160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042501 | TCACGAGTCACTGAG[A/G]TCAGAGACACAAGTG | 221178 |
rs543658152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142652 | CTTTTTTCCTCCTCC[C/T]CCTTTCCTCTTCCTC | 221178 |
rs543660605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122442 | TTACCAGTCTTCATC[A/G]TCTCCATCTTCACCA | 221178 |
rs543670314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037013 | TCTTTTGACCTCCTG[A/G]TCTGCCCACTTCAGT | 221178 |
rs543687299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216436 | GCCAAGACAATCACA[C/T]GCTTGTATGAAATTG | 221178 |
rs543698707 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23996325 | TCTTCGAAAAGTGTA[A/G]AGAATGGTGAGAAGG | 221178 |
rs543724901 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269457 | CAACACTGGAGTGCA[C/G]TGGTGTGATTATAGT | 221178 |
rs543728814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037676 | GCCTTCCAAAGAGCT[A/G]AGATTACAGGCATGA | 221178 |
rs543743410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301605 | GGCTACCGGGTGGGA[C/T]GCTGTGCCTGGGTTA | 221178 |
rs543743659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138725 | AGTAACTGGGACTAC[A/G]GGCTTGTGCCACCAC | 221178 |
rs543778210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175004 | AGTTTAATTCCATTA[C/T]GGTTAGAGAACACAC | 221178 |
rs543787406 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064927 | AATTCTGTAAAATAC[C/T]TGATCAATACTCCTC | 221178 |
rs543791314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275197 | GGACTGGGGCATTCT[A/G]CTCACTGACAGCTGC | 221178 |
rs543806767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158033 | GGAAAGACACATTCT[A/G]GTTTTGGAGATGTTA | 221178 |
rs543839116 | in-del | -/G | 0.178144 | 0.239451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212296 | TGAGACCCTGTTTAA[-/G]AAAAAAAAAAAAAAA | 221178 |
rs543844688 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021194 | AGGAGCTGGCCTCTA[A/G/T]GAAGGGCTGGAGCAT | 221178 |
rs543859705 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045747 | TCATGTTTGCCCTGC[A/T]GAGAGACACAGGCTG | 221178 |
rs543871151 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24183492 | AGGCTTTCACTACTT[C/T]ATACAAGCTTGTCCA | 221178 |
rs543872774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135217 | AATACACTCATTATT[C/T]GAAAAAAAAAATACT | 221178 |
rs543872928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244167 | CCTCCCATGACTTCC[C/T]CCCTTTCGTGTTTGT | 221178 |
rs543876181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129307 | GAGGGAAAGGGAATC[C/T]CAGATCTGACTTTCA | 221178 |
rs543881231 | in-del | -/TT | 0.00952359 | 0.0683454 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148368 | TTTTTTGTTTTTTTA[-/TT]TTTTTTTCCTGAAAT | 221178 |
rs543888488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015214 | TTTTATAGTAAACAA[C/T]GACCTCTGTGACTCT | 221178 |
rs543889670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205141 | CAAATAGGAAGAGAG[A/G]AAGTCAAACTATCCC | 221178 |
rs543897117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096600 | TGTCTAAAAAAAATA[A/G]TAATAACAAGGGGGA | 221178 |
rs543900172 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150712 | TGGGGATTCAGGCAG[A/G]CTTTTGTGTTGCAGT | 221178 |
rs543905254 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164793 | AACGGCACCACAGAA[C/G]CTTTCACAACATCGA | 221178 |
rs543910220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059786 | ATAAGATCATGTCGT[A/C]TGCATACAGAGATAG | 221178 |
rs543911397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027771 | ACCAGTATCATAGCA[C/T]AGTTGTGAAAACCGA | 221178 |
rs543912223 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158391 | CACATTGTGATTCCC[A/G/T]CAGGAATGGTAGAAA | 221178 |
rs543912461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279931 | TTGCTTCCGCAGTGT[C/T]GCTAACTACTAATCC | 221178 |
rs543914634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197569 | TTACCTTTTCTGAAA[G/T]ATAGAAATAATTTGC | 221178 |
rs543934868 | snp | C/T | 0.00143096 | 0.0267102 | missense | SPATA13 | GRCh38.p7 | 13:24249814 | ATGGGACCAACCAGA[C/T]GGAGGAACTGGACAA | 221178 |
rs543937734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985931 | GGAAGCCAGCCTGGG[G/T]ACTAAGTATCCCCTG | 221178 |
rs543943429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241040 | CGATTACTGACATGC[A/G]TGTCACCCCATTCCG | 221178 |
rs543957928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283307 | GGGTCATCTGTTGTA[C/T]AGCTTTCTGTCCCCA | 221178 |
rs543963304 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287020 | TGCCTGGGCTTTCTC[C/T]CCACCTCCACCCCCC | 221178 |
rs543967236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164216 | TTTTCCTCATCTTTG[C/T]ATCACAAATGAAAGA | 221178 |
rs543972759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208326 | GTTCCATATTCCTGT[C/T]AATTAGATGCAAAGT | 221178 |
rs543972920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201630 | GTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 221178 |
rs543976762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015699 | AGCCAGGACACCCCC[A/G]GCCTTCCTGATCCTT | 221178 |
rs543995429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284981 | CCCTCCAAATCTGGT[A/G]TTCCTTTGGCCACCC | 221178 |
rs543998805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001721 | ATGATGGCCGTGGAT[A/G]TGGAGGGAAATGAAG | 221178 |
rs544007571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088755 | GCCAGGTGCTGAGCC[A/G]GTTCTGAGAGCCAAT | 221178 |
rs544009273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247396 | CGTCACTTCTTTAGG[A/T]CCCAGTTTTCCTGAT | 221178 |
rs544033966 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030231 | TTCACACTTGGTGTT[A/G]TACATTCACTGGTGT | 221178 |
rs544035573 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24299525 | CAGCCCGGTGGCCAG[C/T]GTACAGAGCCTGAGC | 221178 |
rs544047018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167353 | GTGGTCCTCTCCTTT[A/G]GTCTGAGAGTTGGGA | 221178 |
rs544048185 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082514 | TTCTATACTCAACTA[C/G]AGCCAAAATAAAAAT | 221178 |
rs544063930 | in-del | -/A | 0.00010022 | 0.00707815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290621 | CCAGAGGCACCCCAG[-/A]AGCTGACGAAGCTGT | 221178 |
rs544065903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044670 | GCCATTTCTTTGTGA[C/T]AAGAACATTCAAAAT | 221178 |
rs544067721 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24214051 | AAGCGATCACCTTCT[C/T]CAGATCCGCATTCAG | 221178 |
rs544085146 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248292 | TCACCATTGTTGCGT[C/G]TCATCCTTCTAAGGA | 221178 |
rs544090333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007126 | CCTCTGGCACTGTAG[A/T]CACCTCTGTCAGTGC | 221178 |
rs544093168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091471 | ATACGGCTGTTAGAA[C/T]AGAATATTCTCTGAG | 221178 |
rs544097792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207357 | ATCTGCACATCCCGC[A/G]CATGTACCCCTGAAC | 221178 |
rs544107121 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24272387 | AGGGGCCTGGGTCAG[C/T]GCACTGCGGAAACTG | 221178 |
rs544109267 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076616 | TTGTGGCTCTGGTGA[C/G]CCGGGGTCTGGGGTG | 221178 |
rs544109327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083111 | TTTTCTGGATGCAAA[G/T]GTGGACAGGCATTCA | 221178 |
rs544118529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182639 | ATGACCCAAACACCT[C/T]CCCCAGGCCCCGCTT | 221178 |
rs544119310 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220133 | GTACCCAGTAGATGC[G/T]CATGAAGTGGGTATA | 221178 |
rs544125681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299012 | TCCCAGCAACAGCCA[C/T]AGATTATTGGTGCAG | 221178 |
rs544126630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001898 | AGATGAGGCTGGAGT[A/G]TGGCTGTGGGAAGGA | 221178 |
rs544129291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254056 | AGAGGAATGGAGATT[G/T]ATTTGAAGGCGATTG | 221178 |
rs544129542 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24244155 | CTCTGCCTCTGTCCT[C/T]CCATGACTTCCTCCC | 221178 |
rs544129651 | snp | A/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24212569 | AGTTGATTCCATATC[A/G/T]TTAAAGTTCTGACAT | 221178 |
rs544135772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292686 | CCTCTGAACTCCTGT[A/G]GAGAGACAGACTTAA | 221178 |
rs544140244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173202 | CCTGCCTCAGCCTCC[G/T]GAGTAGCTGGGACTA | 221178 |
rs544164012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995824 | CAGATAAGCCATGTT[C/T]CCTGAGAACTGGGGA | 221178 |
rs544170046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077147 | TAATAGCAAATAGCT[A/G]TTTCTACCATGCAGG | 221178 |
rs544170627 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24079400 | CCCTGGTTTCTTGCT[G/T]CAGAATGGATTGCAG | 221178 |
rs544171376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152429 | TCTGTGCCTACTTCA[C/T]AGCTCTGTCTGACAC | 221178 |
rs544175060 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24283618 | ATAATTCCTCATTCT[C/T]ATATTTTGAGTTCCA | 221178 |
rs544175522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213432 | CCACCATGCCCGGCT[A/G]ATTTTTATATTTTTA | 221178 |
rs544203809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140874 | TAATCGTAAAGGAGA[A/C]TATTTTAAAAATTAA | 221178 |
rs544204336 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24007675 | AAATGGCTATGGTGG[C/T]CAGGCTGGTCTTGAA | 221178 |
rs544204479 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24028710 | TAGAATTCCAATTGA[A/G]TGTTTGTCCGTTCTT | 221178 |
rs544214752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298378 | CATTGCAGTTAAGGC[A/G]ATGGTACTTCACACC | 221178 |
rs544217147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146556 | ATACATAAACCTGTA[C/T]GATAATTAACACAGA | 221178 |
rs544221375 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073088 | GTTTTTTTAATCCAA[A/G]GCAATGGTGAGTTAT | 221178 |
rs544224771 | in-del | -/AAAAC | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237362 | GTCAGATTCCATCTT[-/AAAAC]AAAACAAAACAAAAC | 221178 |
rs544229601 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24091743 | TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGT | 221178 |
rs544237929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220270 | ATGTCTTGGGCCCTT[C/G]TTTCCTTCTTGGTTA | 221178 |
rs544238949 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191745 | TTGATCTCCTGACCT[G/T]GTGATCCGCCCGCCT | 221178 |
rs544254892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987628 | GAAGGTAAAAGCCCC[A/G]GATTTGAAAAGTTTG | 221178 |
rs544271180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034337 | AGAAAGTTAATAATC[C/T]CTTGTGCTCTGGATC | 221178 |
rs544276202 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062318 | ATATGGGTGAGGCTG[A/T]CATCTTTGGAGGAAG | 221178 |
rs544280936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146904 | ATTTTACAAGCTCCA[A/G]TCTTTTAAAAAATCT | 221178 |
rs544284801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053552 | TTGGTATCTAAGCAC[A/C]CTTATAGACTTCCCT | 221178 |
rs544300361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197147 | AAAAGACCCATCTTT[A/G]GAGGAAGACATATAT | 221178 |
rs544307478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184669 | TTTGTTTTCTGTGCA[G/T]GACAAAGTTCAACGC | 221178 |
rs544310847 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277313 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 221178 |
rs544349357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090784 | ATCCAACATCTGGGC[C/T]CCTTGGACAGTTTCT | 221178 |
rs544350610 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277075 | CAGAGAAGATATACC[A/G]TAAAAGAATTTTGTT | 221178 |
rs544357592 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160842 | AGAGTGCGGCGACCT[C/G]GGGGCTCCGCCGGCA | 221178 |
rs544368107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282610 | GCTGCCCACTCCCAC[C/T]AACCTGTGTTCTCCC | 221178 |
rs544368957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190449 | TGGGCAAAGTAAAGT[G/T]AAAACCTTCTGGAAC | 221178 |
rs544371261 | in-del | -/T | 0.0480646 | 0.147384 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025814 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 221178 |
rs544372592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050344 | TCTGATAATGCTGAC[A/G]AGTCAGTTTCCGGAG | 221178 |
rs544381270 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085809 | GAGTTTCATTTAGGG[G/T]CCAGTGTATTTCCTG | 221178 |
rs544388027 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24268108 | GTCATAAAAAAAGAG[C/T]GTCATAGCCAAATAC | 221178 |
rs544388599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063517 | TCCCAAACATGCCTG[C/T]CAGATTCTCCAGAAC | 221178 |
rs544390373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246885 | AAAGTGACTCAAGGA[A/G]GTGGTTAGAATTTAA | 221178 |
rs544404089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068952 | ATTTTCTCCCATTCC[A/G]TAGGTTGTTTGTTCA | 221178 |
rs544420596 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136571 | AAGAGAACTAGGAAA[G/T]GCTCAGAAAAAACTG | 221178 |
rs544421322 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24087897 | ACTCCTGGTCCCACC[A/G]GTAGTCTTGCCCATT | 221178 |
rs544423122 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24108045 | GGGCACTGGTAGGCT[C/T]GGTGTCTGGATAGGG | 221178 |
rs544429061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225217 | ATGGAGCAGCGAGGG[G/T]TGTGTGAGTGAGTGA | 221178 |
rs544432183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085083 | CGTGGCGATGTTGAT[C/T]TGGAGTGTGTAGTGT | 221178 |
rs544433222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24270656 | CTGTAGCCACTAACC[A/C]TTGGTCACACGGAGT | 221178 |
rs544444680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276585 | AAGAGTGTGAATATA[C/T]TTGACACTGCTGAAC | 221178 |
rs544449507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196443 | CCTGTACCTTTCCAC[A/G]GTGTACTAGAAAATG | 221178 |
rs544469462 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24098306 | CTGATACCTGTAATC[C/G]CAACACTTTGGGAGG | 221178 |
rs544477458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058357 | TAATTATATCAACTC[A/T]TTTAATGCTCACCGT | 221178 |
rs544478429 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142141 | TTTTTTATGCTACAA[A/G]TAGGACAGAGGGGTC | 221178 |
rs544479815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281380 | AGAGGGTGACTGGCA[C/T]CATGCACTCAGAGCC | 221178 |
rs544485243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24252053 | GATGCTCTGTGTGCC[A/G]GGCTGGTGGCTCTAA | 221178 |
rs544488452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239221 | GTTTGTAGAATGGCG[C/T]AGGATTTCAGGAGAT | 221178 |
rs544517457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120198 | TCTGTTTCCGCCTCT[A/G]AAAAAAAAATCAGGA | 221178 |
rs544521906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257653 | CTTTTTTTGCAAGCT[A/G]GAAAAGAGAAGCAAA | 221178 |
rs544542933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058891 | CTGTGCATTTGTTTA[C/T]CCCAGTAATGATGCC | 221178 |
rs544544106 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24115308 | AAATAGCCCCGAGAC[C/T]CAGCAGCTTACAACA | 221178 |
rs544549472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980733 | AGTAGCTGGGATTAC[A/T]GGCGGCCGTCGCTAC | 221178 |
rs544558724 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102009 | ACCCAGAAGTAGGAT[C/T]GTTGGATCATATGGT | 221178 |
rs544576926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178596 | TATCTGTATAAGAAC[A/T]AATAGAGGATCAAAA | 221178 |
rs544610317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015732 | CCTTTGGGGCGACCC[C/T]TGGCAGGCCCCCCCC | 221178 |
rs544611858 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257153 | AGAATTCTTACTTTG[A/C/G]ATTTCCCTTTGTCTC | 221178 |
rs544614843 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158863 | TTGTACAGGGCCTCA[A/G]GGATGCGGGGGTCTT | 221178 |
rs544625657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034790 | TGAGAGGCAGAGTCC[A/T]AGGAGTGATTGTCCC | 221178 |
rs544639845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210335 | AGTGTTATATCCAAG[A/G]ACTTATTGCCAAGAC | 221178 |
rs544640692 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999262 | ACTGGTTTTATAAGT[A/C]TCAAAATCAAGTGCT | 221178 |
rs544641004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097824 | AGATGAAACTGTACA[A/G]TCCAAACGCAGGCGA | 221178 |
rs544646414 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303814 | GGAAGGCTGAGGTAG[A/G]AGAATCTTTTGAATC | 221178 |
rs544656617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068376 | GTACCATACTTTTTT[A/T]ATCCAATCTGTCTAG | 221178 |
rs544656896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108933 | CTTCCCTGCTTGTAG[C/G]CCACACTCCAGCTCT | 221178 |
rs544663049 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24275441 | TGGAATTGTCCCCAG[C/T]CAGAGAGGCGCTGAT | 221178 |
rs544670813 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24112553 | TTCTTGTGCCAGGCA[C/T]ACACACACACACACA | 221178 |
rs544675522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992932 | TCAGCTACTATTCTT[C/T]TGTTTACAATGCAGC | 221178 |
rs544684365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130040 | CAGGAGGCTACTCCA[A/C]ACAGCCCTTTCCTTC | 221178 |
rs544688580 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096616 | TAATAACAAGGGGGA[C/T]CTAATTTGGACAGGT | 221178 |
rs544702715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216512 | TACTTTCAATTCACA[A/G]ACATTGAACTTCAGT | 221178 |
rs544707769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028431 | TGTTAGTTTCTCCTA[A/G]TACTTTACAGATAAT | 221178 |
rs544709534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271197 | TTATGGCACAGTTGC[C/T]TGTTTGGAGTAGAAA | 221178 |
rs544715001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090868 | ATGTCTCACATCTTC[C/T]GTTGAAAACTGGATG | 221178 |
rs544720385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109575 | TAAAAGGGTGACAAG[A/G]TAGAGATAGAGGCAG | 221178 |
rs544721910 | in-del | -/GC | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182509 | AGAGAGAGAGAGAGA[-/GC]GCGCAGGAAAGAGGA | 221178 |
rs544751930 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24118714 | TGTTTCTTAGGGAGA[A/G]GGACCACATGATAGT | 221178 |
rs544764934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274363 | TCCTTCCCCACTACC[A/G]CCACCCAACCTGACT | 221178 |
rs544766286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232547 | TTTAAATTTTTTAAT[A/G]TTTTTCTTTTTTGAG | 221178 |
rs544773477 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980147 | GTGAGCCGAGATCGC[C/G]CCACTCCATCCTCGG | 221178 |
rs544780796 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103841 | TTTCATCCCTTTCAG[A/C]GTTACAGGGTGGTGT | 221178 |
rs544790079 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24268860 | AGTGCGGGTTACTAA[G/T]GCTATGAGTTTCCCA | 221178 |
rs544817186 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098503 | TTGGGAGGCTAAAGT[A/G]GGAGGATCACCTGAG | 221178 |
rs544851766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274079 | GGTCAGCGTGGACGG[A/G]TGGAAGGATTTTGTC | 221178 |
rs544856040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131361 | CCCAGGGCCAAGGAC[C/T]AGCTGACTTCTCACA | 221178 |
rs544857723 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114726 | GGAGTGCAATGGCAC[G/T]ATCTTGGCTCACCAC | 221178 |
rs544860480 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159348 | CAATAACAATTCAAA[G/T]AATTAAATAAAATTT | 221178 |
rs544862471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238452 | GTGAGCCACTGCCCC[C/T]GGCCTCTCCTTGATG | 221178 |
rs544870226 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24199127 | CTCCTGAGCTCAAGC[A/G]ATCCGCCCGTCTTGG | 221178 |
rs544876896 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092546 | AGAGTAAGAGTTTAT[A/G]AGAAAAACAGTTGAA | 221178 |
rs544878073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157131 | AAGTCTGGTCTGTGG[C/T]ATCCAGACACTGACC | 221178 |
rs544891560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086203 | TAACAGGCCCGGCTA[C/T]GTTTGAATTTCAGAT | 221178 |
rs544899915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051825 | GTTCTCCAGGGCAGG[A/G]CAGAGGGAGATGCCC | 221178 |
rs544913045 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216598 | TACTCCTTACACAGA[C/G]AGACCCTGAAGGTAC | 221178 |
rs544915704 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193430 | AGCAGATGCCTCAGC[A/G]TGGTTGAATCTGAGT | 221178 |
rs544920115 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058908 | CCAGTAATGATGCCA[A/C]CTCTGTCTCATGTAG | 221178 |
rs544926617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034879 | ACAGCACCACTCTGC[C/G]ATCATCTATGGCTTA | 221178 |
rs544944112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235478 | GATAAAGAATTGGTC[C/T]GGCTGACGTGGTGGC | 221178 |
rs544947839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125591 | GGAGAATTAAGCAGA[A/G]TTCTCAGTTCACCTA | 221178 |
rs544948243 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103119 | ATTGTCAGGCATAAT[A/G]AGGGCAGAAGAATCT | 221178 |
rs544965223 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24265913 | GCAGGTGGGAAACTT[C/T]GGTGCTGGTCATCTC | 221178 |
rs544981937 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248512 | ATTTAGGATCATAGA[C/G]TCTTGAGCTGTGGGA | 221178 |
rs544995053 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040690 | CCAACTAGGCCTCCT[C/T]TCCTGTGGATCCAAA | 221178 |
rs544996657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290459 | AGCACCCCTTCTCGC[C/T]GGCCAGATAACGCTT | 221178 |
rs544999761 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24120470 | AAAGGAGTTAAATTT[C/T]TCCACCTTTTGCACA | 221178 |
rs545001107 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23991846 | TCTGTATTGTTTCTG[A/G]GAAGAAAAATCTTCC | 221178 |
rs545002348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049872 | AGACATTTTCAGACT[C/T]GTTCTTTCTTTCTTT | 221178 |
rs545006084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302062 | TCCATTTAGAGCATT[G/T]TATTGCTACTCACCT | 221178 |
rs545007521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242293 | GGATGCATGCGCATG[A/G]CTATGTCTACACACA | 221178 |
rs545014750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141934 | TGCAAATGGAGTCAG[G/T]TCTTCATGTTGCTGT | 221178 |
rs545022322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136344 | AGCCGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 221178 |
rs545041828 | snp | C/T | 0.000798403 | 0.0199641 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223530 | AGCACACACCGCTCC[C/T]GCAGCCTCCGCAGAG | 221178 |
rs545045557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284533 | GTAGGCATGATGGTG[C/T]GCACCTGTAAACCCA | 221178 |
rs545056594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130666 | AATAGTTCTTTGTGC[C/T]GATAACATGCTGACG | 221178 |
rs545057054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248040 | GGCCCATGGCCTGAC[C/T]GACAGCCCTTTTTGT | 221178 |
rs545067548 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253890 | AGACGAGGATGTTGC[A/G]GGCTGGGAGGTGGGC | 221178 |
rs545074865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293336 | TTTAAGAAAATGTCC[C/T]GATGGCATGATGAGG | 221178 |
rs545076598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137569 | GTTTGAGGCCAGTCC[C/G]GCCAACATGGTGAAA | 221178 |
rs545083201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289785 | TATTACTACTTAACC[A/G]CTAAAGGATTTCAGA | 221178 |
rs545087167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147541 | TTGCCCTTGTCTTCA[A/T]ATCTCAGCAGGGTCA | 221178 |
rs545093959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050476 | ATGCTGTATAGGATT[C/T]GAGACCCAGGAGCCA | 221178 |
rs545105197 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24029573 | AATATATATTAACAT[A/G]TAGACTGTTCTGTAG | 221178 |
rs545120857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110417 | GATTGATGGAAACAG[A/T]TCCAGACTCACTTAA | 221178 |
rs545133203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169270 | AATGGTGTGCTTGTT[A/T]TACCAGGCTGATGTG | 221178 |
rs545142575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058471 | CTTGGGTGATTACTG[C/T]ATACGGGACAAAGGA | 221178 |
rs545144882 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24228429 | CTGTACTCTTAACAT[A/G]TATGTCAAAAAGAGA | 221178 |
rs545147442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142490 | TGTCTGATGTTTTCT[C/T]CTGTTAGATTGAGGT | 221178 |
rs545147931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085654 | TTTACTCACTTCCAT[A/G]TGGCCCGACTCCCTT | 221178 |
rs545166521 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307061 | GTATATTAAAATTCA[C/T]TTGCCAAACTCGTTC | 221178 |
rs545182091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104300 | GTTTTGACAAAAAGG[A/G]TTTTACTTCATCTTA | 221178 |
rs545182751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045155 | TTCTGACAAAGTTGT[A/G]TGTTTCTGTGGCATT | 221178 |
rs545191883 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109764 | TAATTCCCTTAACCA[A/G]CACCACTAGGAGGTT | 221178 |
rs545222755 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064525 | TGTGTTTTTATAAAA[C/G]AGCCCCCAGAGAACT | 221178 |
rs545224739 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137814 | CAAGAAGTACTGTGC[C/T]CTTTGACTATTTTAT | 221178 |
rs545232888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229521 | AGCCCGCCCTTTGAC[A/G]CTGACTGCCCACTGT | 221178 |
rs545236046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279863 | CCCTGGCCTCTGCCC[C/G]CCATCTCCTGGCCAG | 221178 |
rs545265645 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207759 | ACCTGCTACCTCTGC[A/G]CATCACCCAAGATGC | 221178 |
rs545283482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228497 | CATCTTATACACTGG[A/G]AATGTTCGGTGTTAC | 221178 |
rs545290832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221648 | TGTGGGAAAGTATGT[A/G]TACAGGTGTGTGCAG | 221178 |
rs545300934 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265719 | CATGCTTTCCCAGGG[C/G]ACAGCATGACTCTCC | 221178 |
rs545302609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080593 | TTAGTGTGGACAGGC[C/T]GCACACCACCTAAGA | 221178 |
rs545303669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053126 | GTTTTTCTCCGTGAC[A/G]TTCTTGTTTTAGATA | 221178 |
rs545306412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073770 | GCTAGTTTCTGTTGC[A/T]TGCAACAAGAACCTT | 221178 |
rs545314070 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216853 | GTCAGGAGTTTGAGA[A/C]CAACCTGGCCAACAT | 221178 |
rs545322130 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104151 | AGTCTGCTCACCACA[-/T]TGTGTACGTGCTGAG | 221178 |
rs545328100 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305919 | CAGAATCCTGGAGCA[A/G]TAGATTTCTTTGTCT | 221178 |
rs545336620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146977 | CACTTAGAAATAAAG[A/G]GAAGAAAACATCTTG | 221178 |
rs545343113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234516 | GCTTGGTGACACCGA[C/T]TGATTTGGCTGTGTC | 221178 |
rs545349052 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24035577 | CACACAGCCTAACTC[A/C]GAAGAAAATAAGAAA | 221178 |
rs545353257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037934 | TTTTTTTTTTTGAAA[C/T]GGAGTCTCGCTCTGT | 221178 |
rs545361591 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24199136 | TCAAGCGATCCGCCC[A/G]TCTTGGCCTTCCAAA | 221178 |
rs545362100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992960 | AGCATGGGAATTTCC[A/T]TCAAGCCAGCTGTGC | 221178 |
rs545380998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241822 | TTTGAGAGGCCGAGG[C/T]GGGAGGACTGCCTGA | 221178 |
rs545386323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246491 | CAGAAGACAGATTAG[A/C]AAAAGAAAAGACATG | 221178 |
rs545390874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069036 | TGTAGTATATTCTTG[C/T]GTAGTATAGTCAGGT | 221178 |
rs545397501 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159476 | GAATGGAAAGTACAC[A/G]GAGTTCTGATGTACT | 221178 |
rs545408001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126803 | CTCAAGAGATCCACC[C/T]GCCTTGGCCTGTCAG | 221178 |
rs545420397 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24178483 | AATTGCTTCTTGGCC[-/T]TTTTGGCTATGATCA | 221178 |
rs545444869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174874 | GTGAGCCCCTGCACC[C/G]AGCCTAAAAGTTTCC | 221178 |
rs545446617 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245829 | CCTGGGCTCAAGCAA[A/T]CCTCCTGCCTGAGCC | 221178 |
rs545453877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203267 | GTATAAAGAACCATT[A/C]TGTAGAGGATGTAAA | 221178 |
rs545471173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144749 | TTCTTGACCAGGGTC[A/G]GAAGAGGCAGAGACT | 221178 |
rs545472832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180092 | TGCCTAATCCAAGGC[C/T]GTGAAGATTTTCTCC | 221178 |
rs545487400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259487 | GTGGTTTCAAAGTAC[A/C]ATTGGGGATTATCAT | 221178 |
rs545506539 | snp | C/T | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304479 | TTTTTTTCTAACAGG[C/T]CCATGTTTGAGAATA | 221178 |
rs545513655 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209154 | TAGGTGCCCAAGAAC[C/T]GTACTCAGGACAAGC | 221178 |
rs545526641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24032115 | TTATCCTCCACCATC[C/T]CCCAGGTGACGTCTG | 221178 |
rs545529837 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098617 | AAAAAAAGAAGAAGA[A/G]GAAAAGAAAGAAAGA | 221178 |
rs545530627 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106551 | CTGTAGGTGCATTGC[G/T]CAGCAGTGGGTCACC | 221178 |
rs545532477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980889 | GAGCCACTGCGCCTG[A/G]CCAACAAAGTTTTTT | 221178 |
rs545537291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139960 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 221178 |
rs545539638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060723 | TCCAGCATCTGTAAG[G/T]AACTTAAGCAAATTT | 221178 |
rs545546163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294431 | TATTAATGAAAGTCA[C/T]CCATTGTCACCGTGA | 221178 |
rs545550618 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017038 | GTAGTGAGGAGCGCC[C/T]GAAGTGTGGGAGGAG | 221178 |
rs545555406 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173484 | TCTTTCCCATCCATA[C/G/T]GCCTTTTATTCCCCC | 221178 |
rs545570038 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24281013 | CACACCCCCAGCCAG[A/C]CAGACATGGGTACAC | 221178 |
rs545587896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257043 | CAGCCTACCTAAGCT[A/C]CTAATTTTTTTGTAC | 221178 |
rs545589329 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24176220 | GCAAAAAGTTACTTA[C/T]GCCTGTCTTTTCCAT | 221178 |
rs545610355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298118 | TAAATCCAGCACTTT[G/T]GATGCCACATGCAGG | 221178 |
rs545613700 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24053798 | CCAAAACAACCCCTT[A/T]GTTTTCTTGATGGCT | 221178 |
rs545631960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300132 | GGGAGCGTCGGGCTT[A/C]ACACAGACATTCTGC | 221178 |
rs545650727 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003906 | TTAAACAAGAACCAA[C/T]ACAGCAGAAGTCCCT | 221178 |
rs545654306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093120 | AATCCATCCATTTTC[C/T]ACCTGACCCTAATAA | 221178 |
rs545670906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299546 | GAGCCTGAGCCTGAC[A/G]TCAGGACAGTCTGGG | 221178 |
rs545679374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086893 | AGCGAGGTCAGAGGA[A/G]CAGCCCAGGAGGGAA | 221178 |
rs545686072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134671 | AGAACCACTGACTTG[A/T]AAGAGCAGCTGGTCG | 221178 |
rs545691912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046578 | GGCCTCTTTCACTCA[A/G]TATGTTTGCAAGATT | 221178 |
rs545702833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056175 | ATAGAGGAAGTGAGT[C/T]AGTTTGTATCAAATG | 221178 |
rs545705978 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24043774 | GCAGCATGTTTTCCC[A/G]ATTCTGTGCTGATTC | 221178 |
rs545711689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158544 | TGCGCCGCCTCTTCA[C/T]GTCAGATCAGTGAAT | 221178 |
rs545733297 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24042366 | AAGTTGGAAAGCCAA[C/T]GATGCAGTTCTAGCC | 221178 |
rs545743197 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128721 | TTTAAACATAAAAAA[A/C]GTCCTACCTTATTTA | 221178 |
rs545746659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012337 | ATGAAACTCTCTTCT[A/G]TCTTGGTCAAGGTTG | 221178 |
rs545748218 | in-del | -/TAAATAAATAAATAAATAAATA | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202071 | GAGCAAGACTCTGTC[-/TAAATAAATAAATAAATAAATA]AATAAATAAATAAAT | 221178 |
rs545770123 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24147886 | TTCATTTCATTTAGC[A/G]TAAGGTCCTCAAGGT | 221178 |
rs545789205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200652 | GAATAGCATAACATA[C/T]GAGATGTGAATATAA | 221178 |
rs545794512 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190271 | TATACATAATATATA[A/T]TATTATATATAATAT | 221178 |
rs545796401 | in-del | -/C | 0.0759472 | 0.179459 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057027 | TCTCTCTCTCTCTCT[-/C]TCTCTTTCTTTCATA | 221178 |
rs545798641 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262081 | GGGAAGATTACACAT[C/T]AGAAAATTCCGTTTC | 221178 |
rs545821164 | snp | C/T | 0.000514536 | 0.0160313 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302919 | GAGAAGGTCTTGGAA[C/T]CACCTTCAGTCTTTG | 221178 |
rs545829311 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24126627 | AGTGGTATGAATATG[C/G]CTCACTGCAGCCTAG | 221178 |
rs545832955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112672 | TTATATTATCACTGT[A/G]TAACAGGAGGTGCTG | 221178 |
rs545833108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083893 | AGATGCAGGTGCTCT[C/T]CTGACATTTTCCTTA | 221178 |
rs545839782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996248 | GGAGAGTCCGCCGCC[A/T]TGCCTTTCCACCTTC | 221178 |
rs545846895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166497 | TGGGCTCCAGCTTGG[G/T]GACTTGAGGGACCCT | 221178 |
rs545848930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071640 | GGTGTCTGACCGTAC[A/G]TACAAACAGGCACAC | 221178 |
rs545853952 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24277260 | CCATCCTGGCTAACA[C/T]GGTGAAACCACGTCT | 221178 |
rs545876461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043236 | GACATGCGTCTTGGC[A/T]ATGACAAACATGCAA | 221178 |
rs545876543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990012 | CTGTTGTTTATAAGC[A/C]ACCCAGGTTATGGTA | 221178 |
rs545892517 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24168687 | TTCAAAGGAATTGCC[A/G]TTGCTTAAATGTTCC | 221178 |
rs545900080 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24171798 | CCTCAGCTGGAGGAA[C/T]GTTGGGAAAGTCAAC | 221178 |
rs545911225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292503 | AAGTCTTTAACTGCA[C/T]CTGCAGCTCTGGAGA | 221178 |
rs545922639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171624 | TGTGCTGACTTCCAC[A/G]TGTTCAGACAGACTT | 221178 |
rs545942100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056683 | GCTTCTTCGGATGGC[C/T]CTGCCTTCTTAGCTG | 221178 |
rs545943103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211965 | CACCAGTGCTCCCCA[C/T]GTGGCTGGAGCTCTC | 221178 |
rs545957661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206129 | AGAAACCAACAGTGT[A/G]AAGAGACAATCTACA | 221178 |
rs545961228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984524 | CCTGTCCTTCCCACC[A/G]TGAGTGGTGGAGCTG | 221178 |
rs545970254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151220 | TGTGCTGTGATTGTG[A/G]GCATGCGTCCTTCAG | 221178 |
rs545975844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230313 | AGCTGGTGAGAGGAA[C/T]GTGTGCAGGTCATTA | 221178 |
rs545984441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194563 | TCTGAATCCGTAACA[A/G]TTTGAGGATTTGGTA | 221178 |
rs545990257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072992 | ATTTTAAGCTGAACC[C/T]GTCCAACATTGATCC | 221178 |
rs545996631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113464 | AAAAAATTAGCCAAG[C/T]GTGGTGGCATGTGCC | 221178 |
rs546010307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262951 | AATACATACGTTCAG[G/T]TTATTTTAAAAAAAA | 221178 |
rs546013595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178030 | CCTGGCAAATTTCGT[G/T]TTTTGTAGAGATGGG | 221178 |
rs546022944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205263 | AGAATACAAAACCAA[C/T]GTGCAAAATTGCTAG | 221178 |
rs546031588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145628 | GGACTGGGGAACTCT[A/T]CCTGCAATTCTCAAC | 221178 |
rs546034694 | snp | A/T | 0.000711997 | 0.0188545 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303252 | CTGGTCACACTTAGA[A/T]ATTGAGCTCTTACTC | 221178 |
rs546046560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095839 | AAAACCGTCATTTCT[A/G]TCTATGAAATGGGTC | 221178 |
rs546049430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992144 | CTCCCTGACACTCCT[A/C]AAGTCTGGGTTCTTG | 221178 |
rs546050021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280429 | CTTCGAGGAGAAAGC[A/G]TCATTTTTCAGAGCT | 221178 |
rs546050804 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977910 | CTTTTTTATTTATTT[A/G]TTTATTTTTTTGAGA | 221178 |
rs546074848 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244188 | TCGTGTTTGTCTGTG[A/T]CCAAATTTCCCTCTG | 221178 |
rs546076281 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184509 | CACAAAGATTATCAC[A/T]TTTTTGGTGGTAGTG | 221178 |
rs546089208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285474 | GCTAAGTGAGCAGCT[A/G]GTACTTTTTTAAAAA | 221178 |
rs546091734 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260033 | TATTATAAATGAGGC[A/C]CAGTACCAGAGGCTG | 221178 |
rs546100664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102835 | TTTGCTTTTGTTGCC[A/G]ATGGTTTTGGTGTTA | 221178 |
rs546130844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090020 | GGACCTAATCACCTC[C/T]TAAAGGCCCCACCCC | 221178 |
rs546137931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985978 | GCTTCTCCTCACCCG[C/T]GGACCTCAGCTCTTC | 221178 |
rs546138143 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24274616 | AGCAGCCCGTGACAG[C/T]TGCTCCCAGCTGTGA | 221178 |
rs546145373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122793 | AGCTGCCACATCTGT[A/G]GAGACTCTCGTTGTC | 221178 |
rs546150337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026170 | ATGATTTTTCATGTC[A/G]TTTTATGGTATCATG | 221178 |
rs546157391 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189414 | AGGGGGCGGAGCTTG[A/C]AGTGAGCTGAGATCA | 221178 |
rs546158484 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24280059 | CTCTGTTGCCCAGGC[G/T]GGAGTCTGGTGGTAC | 221178 |
rs546173339 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167847 | ATTCATTCTTCCTTC[-/A]ATTCATTGTTTTATT | 221178 |
rs546177859 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049715 | GAAGGGAGTGGATGA[A/T]CTGTTTGTCAGCAAG | 221178 |
rs546190224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153531 | ACCCTTCAGATGACA[A/G]AATCAGTGAAGGCAG | 221178 |
rs546190237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014984 | CAAGCTCCACTTCCT[A/G]GGTTGATGCCATTCT | 221178 |
rs546198139 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171966 | GATCATTCGGAGGGG[-/T]TACTCAGATTCTCCG | 221178 |
rs546198730 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000600 | AGTCTATGAAGTGGT[A/G]GAGAAGACGGCCCAA | 221178 |
rs546199769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239562 | TAGCCAGGCGTGGTG[G/T]TGTGCACCTCTAGTC | 221178 |
rs546207820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170385 | ATTTTTGTTGATGTC[C/T]TACCATAGGAGTCTA | 221178 |
rs546214678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24043889 | AATAAGGACTGCCAG[A/G]GGAGGGGTAGGTGGC | 221178 |
rs546219975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195078 | TAGCACCCCGCAAAG[A/G]AACCCCAATTCCTGT | 221178 |
rs546225418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008747 | AAACCTTTGGCCCCC[A/G]GCTCCCTGTCCACCC | 221178 |
rs546237067 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23986771 | AAAGAGCATCGGGGC[C/G]ATACAGCAGTCATTT | 221178 |
rs546248654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237530 | TAGAGTAGTCATTGC[C/T]AGGGGCTGTGGGGGA | 221178 |
rs546265132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280831 | ACCCCCAAACTCACA[C/T]ACCAGCAAAGCATAC | 221178 |
rs546265427 | in-del | -/TTTC/TTTCTTTTC | 0.493201 | 0.0579089 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118912 | TTTCTTTTCTTTTCT[-/TTTC/TTTCTTTTC]TTTTTTTTTTTGAGA | 221178 |
rs546267971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299172 | GCAGGCCCTGAAGTC[A/G]TCTGTAAGTCAGAGT | 221178 |
rs546272389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118844 | CACACGCTGGTTCCC[A/G]TGTTCAGTAAGAACT | 221178 |
rs546285162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148634 | GGCTTTTAGTCAGAG[A/G]GAGAACTTGGTTGAA | 221178 |
rs546329912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247674 | ATTTTAGTAGAGACA[A/G]GGTTTCACCATGTTG | 221178 |
rs546330498 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152084 | TCTTAGTCTGTTCAG[C/G]CTGCTGTAACAAAAT | 221178 |
rs546332907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048734 | GAACCGTTTAATATC[A/G]GAGTGCACTCTCATA | 221178 |
rs546348483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128305 | ATTGTGGCTTCATCA[A/C]CAGAAATGCTCTGCC | 221178 |
rs546357983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158064 | TGTGGAACAACAACA[A/G]AAAAAGCGCGTTAGA | 221178 |
rs546367885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049232 | ACAACATTTTAGTCA[C/G]TGATGCCTCGCCTAC | 221178 |
rs546387834 | in-del | -/CATT | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083120 | GCAAAGGTGGACAGG[-/CATT]CATTCATTCCAGCCT | 221178 |
rs546400945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250418 | CCGGGTATCCAGTGA[A/G]CACTTTGAAAATACA | 221178 |
rs546407892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227083 | CCAGTTCTGTTGGCT[C/T]CTGTTTGTACAACTG | 221178 |
rs546409568 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122642 | CTTTTTGCACATACT[G/T]TATATCACTTCAAGA | 221178 |
rs546414785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197246 | AAGTATAAAATAATA[C/T]TGAGATAAAAATTTT | 221178 |
rs546417352 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24073008 | GTCCAACATTGATCC[C/T]GTAGATCTTGTCTCT | 221178 |
rs546421341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164917 | CAGCCGTCGCGCTAA[A/C]TTCGGGGTTGTGGAC | 221178 |
rs546422098 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24131159 | AGCTGTATTATTTAA[A/G]TCCACTTATTAGGTG | 221178 |
rs546426469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108130 | TGCTGTGCCATCGCC[C/T]GGCTGCAGGGGGAAG | 221178 |
rs546435357 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260346 | GAAAATTACACTGGT[C/T]AGGTCACAGTGTCCT | 221178 |
rs546440996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170801 | GATCCACTGAAAGAC[C/G]TGGAAGCACCCTTTT | 221178 |
rs546442996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067773 | GCAGTGACATGATCT[C/T]GGGTCACTGCAACCT | 221178 |
rs546444481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069217 | TTGCTTTGAGCAGTA[C/T]GGCCATTTTTACAAT | 221178 |
rs546451116 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24110502 | TAGAGATGAATTGCT[G/T]CACTTGAATCTGCAT | 221178 |
rs546460665 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24235863 | CTCATTTGGGATTTT[-/A]AAAAAGTAACTGTTT | 221178 |
rs546475482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210924 | AGTTTCTTTCATCAA[C/T]GTTTTATAGGTTTCA | 221178 |
rs546485726 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982766 | AGAAGTTGAACGAGT[A/C]AGACAGGGTCACCCA | 221178 |
rs546486225 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24150429 | GGTGCCCTCTGGGGA[C/G]ACCTGGTTCAGGCAG | 221178 |
rs546488855 | snp | A/G | 1.86163e-05 | 0.00305087 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249868 | GTGTGCACTTCCCCA[A/G]GCCAGCAGAGGCCCT | 221178 |
rs546490312 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196960 | TGAGCAAGCTGCTGA[G/T]TACGGGGTGAGTAGT | 221178 |
rs546500422 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987906 | ACGCAACGTTCTTAA[C/G]GCCCAGGTATGTTGT | 221178 |
rs546504407 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176548 | CAAACTAGATCCTTT[C/G]ATTAATGGGACCAGG | 221178 |
rs546512385 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24092280 | TTTTCTGGACATTCC[A/G]GCAGCTCTCTAAGGA | 221178 |
rs546521315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287823 | TGGTATTTTGTGCTT[C/T]TATGGATTGTGTACG | 221178 |
rs546547872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151315 | ACACATGGGGCTGAG[A/G]ACCCGGAACCATTTG | 221178 |
rs546549606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072057 | ATAAAAGAAGTGCAC[A/G]TGTCCAATCAAGAAT | 221178 |
rs546573279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282679 | TCTTCCTCCACGTCG[C/T]AGCAAAGTCTGTCAT | 221178 |
rs546592117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060773 | CTCCATTAAAAATGG[A/G]CAAATGCGGCTGGGC | 221178 |
rs546596996 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180397 | TCTTGATTCCTGTGG[C/T]TTTATAGTAAGCTTT | 221178 |
rs546597204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984174 | GGTCTTGTGGTCAGT[A/G]TCTTGCCCTTGGCTG | 221178 |
rs546612742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019913 | GTCTCATCTCTCTCG[C/T]CCTGGAGTCTTTCTG | 221178 |
rs546612834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066880 | TGGCAGACTGGTAGA[C/T]AGCCATAGAACTGCA | 221178 |
rs546623006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257973 | AACGTGCTCTGAAAC[A/G]ATAAGAATTCTGGAT | 221178 |
rs546626040 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129905 | TAACCTTAGGACCTC[A/C/G]CAGGACCCTGGGGTC | 221178 |
rs546633228 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299320 | CCTGTGGCCAGTGCT[C/G]AGAGATGCAAGTGCA | 221178 |
rs546638960 | in-del | -/CTTAGATA | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095622 | AAAAAGAAAAACCAC[-/CTTAGATA]CTTAGATAACAGTAA | 221178 |
rs546639175 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977637 | GGCCACTGAAGTCCA[C/G]CCTGGGCAAAAAAGT | 221178 |
rs546641335 | in-del | -/GG | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024357 | GATGAATGGATGGAC[-/GG]ATGGATGGATGGATG | 221178 |
rs546641432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227882 | GCCTCAGAATTCTTA[C/T]ATAGCACATCAGGCT | 221178 |
rs546645801 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188755 | AGAGGAAGAAGATGC[C/T]ATTCTAGGATTTTTC | 221178 |
rs546664808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095444 | GGGAGTTAAATTTAA[C/T]GGGTACAGAGTTTTA | 221178 |
rs546664896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265439 | CTCGATGATTTAGGG[A/G]AATGGACATTGGCCT | 221178 |
rs546670386 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24109035 | TGTTACATATGTATA[C/T]ATGTGCCACGTTGGT | 221178 |
rs546674306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067464 | CTACTTTTCCATCAA[A/G]TACCAAGCCCACGTT | 221178 |
rs546679251 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24041650 | TTCTTAGTGGGAAAA[C/T]ATCTATCAGAAAGTA | 221178 |
rs546682547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292731 | GGCCGGGCGCCATGG[C/T]TCACGTCTGTAATCC | 221178 |
rs546703549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272849 | GGCTCTCAAGAGGAT[G/T]TATTCCAGCGCTGAG | 221178 |
rs546703575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264978 | GGGTTCATTGAAGCC[A/G]CTGAGAGCACATATT | 221178 |
rs546720599 | in-del | -/AA | 0.315952 | 0.241144 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100143 | ATTTTTAAATAGTTT[-/AA]AAAAAAAAAAGAATC | 221178 |
rs546727510 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066393 | GACTCAGAGTTTAAA[G/T]GATTTGCCCAAAGTC | 221178 |
rs546734965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173034 | TTTTGTTAGATTAAC[A/G]CCTAAGTAGTTCATT | 221178 |
rs546734996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991727 | CCAAGAGGACAACAG[A/G]GTAATCATCCCACAG | 221178 |
rs546739409 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206817 | GAATCACTTGAACCC[A/T]GGGGGCAAAGGTTGC | 221178 |
rs546757770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096892 | GTGACCTCTTGCCCA[A/G]GTGTAAGGAGATGCT | 221178 |
rs546767479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061348 | AACTGCCATTTGACC[C/T]AATAATCCCATTACT | 221178 |
rs546789002 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272465 | GACAACAAGCACCAT[A/C]TTTAAAACAAATAAT | 221178 |
rs546792035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020912 | CTGGGCATGGTGGTG[A/G]GTGCCTATAATCCCA | 221178 |
rs546802099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257230 | GATTAGCTTGCTTTT[C/G]TTATCTTCCAGAGAG | 221178 |
rs546809736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191399 | AAACTTTGTGTGACC[C/T]GCTTTATTTCGATAT | 221178 |
rs546809882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084048 | AGGTTTTCTGGATTA[C/T]AGTTTAACAAGCGTT | 221178 |
rs546810254 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298450 | CTGCTGACCTGGAGG[A/T]GCAGTGTGGCCCCTG | 221178 |
rs546813389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117828 | ATGTCATTATGTAAA[A/G]AAATATTTTTTGTTT | 221178 |
rs546819026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090512 | CTGAGCTTTGACCTC[A/G]CCCTCTTTTTTCCCA | 221178 |
rs546819442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002292 | ACATGTTGAATGACA[A/G]GTATCTACCAGTCTC | 221178 |
rs546829101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184744 | ACCTAATATAAAATC[A/G]TGTCCACCATGGTAT | 221178 |
rs546838322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161021 | TTTGAGTCCCAGTGG[A/T]CTGCCTCGGGGCTTC | 221178 |
rs546852508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277210 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 221178 |
rs546870645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240543 | GCTGGGATGGAGTTT[C/G]TCACCGTCATGCGGA | 221178 |
rs546873159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078253 | AAGAGAGGCAAAACT[C/T]TGGAGCCAGACACGC | 221178 |
rs546875207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038289 | ATCTGCTATAATGGG[A/G]TCAGAAAAGGCCACA | 221178 |
rs546876097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270708 | TGGGCAGGCTCTGGC[C/T]GGGAACGCATACAAC | 221178 |
rs546876130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009241 | TGGTCCAGCAAGGAG[A/G]GCCACCCTTCTCCCA | 221178 |
rs546892514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184257 | TCCATACAGAAAATT[A/C]TCTGGGAAAAATGTT | 221178 |
rs546895911 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281309 | CACAGACACAGGCCC[-/TG]TGACCTTTCCTGACC | 221178 |
rs546898161 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303960 | TGCAATATAAAAAGC[G/T]CATTTACTGTAATAT | 221178 |
rs546914047 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24075119 | CCAGGTCCTGTGCCC[C/T]AGTCCTGCTCTGCTA | 221178 |
rs546916440 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089944 | TTTCACATGGCATGG[A/G]CTTGTCCCCTCAAAC | 221178 |
rs546918551 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175824 | TTCTCCCACAGGAGA[G/T]AAACTTTAGAAATCC | 221178 |
rs546932037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246946 | AAGAGAACTTAAGGG[A/G]AAACAAGTGACTTTT | 221178 |
rs546935969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113083 | CACTGAGGGACTTCT[C/T]GGCTCTCTTTCCTAA | 221178 |
rs546940439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282062 | TGCCAGACTCCTGGG[C/T]TCTATTTACAGAATT | 221178 |
rs546941681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198611 | CAGTTTACATCAGTT[C/T]CTAGATAAATGTTGA | 221178 |
rs546953131 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101613 | TTGGAAAACTTGTAA[-/CT]CTATATTCACTGAAC | 221178 |
rs546953494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015754 | GCCCCCCCCCAATTC[C/T]TAGGTCCACCGTTTC | 221178 |
rs546955789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285514 | CTGCCTGCCTGCCTT[C/T]CTCCCTCCCTCCCTC | 221178 |
rs546959013 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24226871 | ATCGCAGAGTACTTT[A/C]AGATTGAGATTAGTC | 221178 |
rs546980203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190556 | GATTCCACCCCTCAT[C/G]GATGACTTTGAGGGG | 221178 |
rs546993891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246594 | GCCGGGTGTGGTGGC[C/T]CACGCCTGTAATCCC | 221178 |
rs546997917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113607 | CTGGGCGAGGTGGCT[C/T]AAGCCTGTAATCCCA | 221178 |
rs547006608 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232083 | TATGAAAATCGGCTG[A/G]TGTGATTAAGGCCAA | 221178 |
rs547008858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075314 | TACATAATTATATCT[C/G]CAGAGCCTGGATCTC | 221178 |
rs547009247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069351 | CCTCCCTGGTTAGCT[A/G]TATTTCTAGGTATTT | 221178 |
rs547044646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033795 | CCATCCAGCCTGTGA[C/G]TTCCTCAGGAAGTCA | 221178 |
rs547045434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280165 | TACAGGTGCGTACCA[C/T]GACCCCGGGTAGAGC | 221178 |
rs547053890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140596 | AAGCTCAGTCTCATG[C/T]GTGCCCCTGCTCTTG | 221178 |
rs547064838 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24213063 | TGCTTGGGTCGGCCC[A/G]TCTCCACAGCACCAA | 221178 |
rs547076407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102597 | CTCCTTCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 221178 |
rs547088855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172462 | AGGTTTTCTTTTGTG[G/T]TTTTTTCTAAAACGT | 221178 |
rs547098985 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061873 | ACATAAAAGTTTTTA[A/T]AAAAAATTAAAAATT | 221178 |
rs547111511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212315 | AAAAAAAAAAAAAAG[A/G]TCGAGGGAAACAAAC | 221178 |
rs547122386 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068552 | CTTTGAAGAATCACC[A/G]CACTGTCTTACACAG | 221178 |
rs547131430 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110648 | GGGCCAGACACTGGG[A/C]TAGATCCTGCGGACA | 221178 |
rs547145008 | snp | G/T | | | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256369 | TAAATGATAAGTGCT[G/T]GGGGTGATGATATGC | 221178 |
rs547156605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219960 | CCTGAGATACCCTTC[A/G]TTCCTGGGTCAGTCA | 221178 |
rs547165298 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982073 | TGTAAAGATGTGTGT[G/T]TTTTAAAGTACTGTG | 221178 |
rs547186739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056591 | CCTACTGCTGCACCC[A/G]CAGAGCCCAGCACAG | 221178 |
rs547196641 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104413 | CAATTCTCAAGGCAG[G/T]CATAAATCCGCTAAT | 221178 |
rs547207427 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24163062 | CCATGCTATCAGTCT[A/G]CTTTCCCTCTTAGCC | 221178 |
rs547210372 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006934 | GCTGTGGCATTGCCT[C/G]GGCTTTGTCACAGTT | 221178 |
rs547221228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263304 | TTGCGTGATAGCAGC[A/G]GAGCTCTCAGGAAAG | 221178 |
rs547221253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015435 | TCAAAGTACATGTGA[A/G]GAAAAACTAATTTCG | 221178 |
rs547228124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135866 | TCATCTGGAGTGATT[C/T]CTCAGCCCGACCTGA | 221178 |
rs547228258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129554 | AGTAGGGACAGGTTT[G/T]TTATTTGGCTGAATC | 221178 |
rs547229264 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303453 | GGTCCTCAGTGCAGA[C/G]CAACTTACGCATCCT | 221178 |
rs547232793 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24276743 | ATAATAGCTTTACAG[C/T]GTCAAAATTCCCTTA | 221178 |
rs547255453 | in-del | -/TGT | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203161 | ACAGGCCCCAGTGTG[-/TGT]TGTTCCCCTCCATGT | 221178 |
rs547264392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254347 | TTACCCTTGGTTTCC[A/G]GCCCTGCATCTTCTG | 221178 |
rs547268533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011976 | AAAACTCACAGGCAC[A/G]GGGACCGGGGCTTGC | 221178 |
rs547292647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059104 | AGCCTTCCGAGTAGC[C/T]GGGACTACAGTCGCC | 221178 |
rs547296669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295054 | TCGACTACTTTATAC[C/G]CCACTCCCATAAGAA | 221178 |
rs547303767 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170423 | TTTAAAATTTTTGTG[G/T]GTGGACACTACTCAT | 221178 |
rs547315247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017591 | AGATAGACCCTGTCT[A/G]GCATTCCGATTTAAC | 221178 |
rs547347888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224615 | GTCCCTCATGTGGGC[A/G]ACCCTCCTGCGGGAA | 221178 |
rs547350119 | in-del | -/ATT | 0.0178098 | 0.0926698 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054923 | TCCCAGCATTTAAAC[-/ATT]ATTAAGTCAATTTAG | 221178 |
rs547350429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005718 | GAACACACGAGCTGT[A/G]GAGGGGCATTTTCTG | 221178 |
rs547360450 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291312 | GCAGCTCGGCTCAGA[A/G]CAGGATTCTTTATGG | 221178 |
rs547362976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164383 | CCAGGGAACCTGCAG[G/T]GTATTGTTGAATTGT | 221178 |
rs547365023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110150 | TTTCTTTACCTTCTC[A/T]GGCTTTCCAGAGGAA | 221178 |
rs547382336 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24251512 | GAGGCTGCAGGGTGC[A/G]GGCCAGTAAGCTGAT | 221178 |
rs547386546 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181348 | ACTATAAGCTTGTTA[C/T]TTTATAAATTTTAAT | 221178 |
rs547391902 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142322 | TTACATCCTTTTGCT[G/T]GTTCAGGTTACAGTC | 221178 |
rs547409193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24127035 | TCTGAGACCAGTTCC[A/G]AGGTTTGTATAATGA | 221178 |
rs547413018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035894 | ATGGCTCACGCCTGT[A/T]GTCCCAGCTACTCAG | 221178 |
rs547420688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994180 | TGTTCTAAAGGAAAC[A/G]CTACTGTGAAAGGAT | 221178 |
rs547426498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104157 | GCTCACCACATGTGT[A/G]CGTGCTGAGAAAATC | 221178 |
rs547432243 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23994757 | CTCAGTTTTGGAAAC[A/G]GAAGAGTAGAATTCT | 221178 |
rs547444676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210409 | TATGGTTCCAGGTCT[C/T]AAGTTTAAGTCTTTA | 221178 |
rs547444897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087691 | CCCTCTCTACACACA[C/T]GCTTCTCTAGGTCAC | 221178 |
rs547447159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187456 | CAGCGACCGGCTTAC[A/G]TTTTATTCTGCCTAG | 221178 |
rs547452260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156884 | TTGGGTCTTGCCTTA[A/T]GTGCCAGAGGCATCT | 221178 |
rs547453485 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029247 | TCTTTTCGTGGGAAT[A/G]CTTTAAAGTCTGGGG | 221178 |
rs547463420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228894 | TTTATATCATACTGT[C/T]CTAAAAATAACAAAA | 221178 |
rs547493544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254718 | GGTTCCTGCGGGGAA[C/T]CGTATCATCAGCTTT | 221178 |
rs547501111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241859 | GAGTTTGAGACTAGC[C/T]TGAGCAACATAGTGA | 221178 |
rs547503791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295520 | GGGAGGCTGAGTTGA[A/G]AGGATCACTTGAGCC | 221178 |
rs547505099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111481 | GGTGCAATCACGGCT[C/T]ACTGCAGCCTCAACC | 221178 |
rs547511479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082259 | CTCTCTCATAAGCAC[A/G]TAAGTGTTCTGTGGC | 221178 |
rs547513541 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154560 | AGGGAGTCTTTTGAG[A/G]CGCTAGAAATTTTCA | 221178 |
rs547515640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273551 | CATTCTGGAACATGA[A/T]ACATATTTCATACTT | 221178 |
rs547523892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235099 | TTGTTATGATTGAAA[G/T]TATTTCCTTTGGTCA | 221178 |
rs547540310 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042148 | CTGTGTCACGGGAGC[G/T]TTGGCTATGACCACC | 221178 |
rs547540501 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212507 | CAAACCACCTGACTC[-/TG]TTGCATCAGGATACT | 221178 |
rs547553320 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216650 | TTCTTTCTTTTACTA[A/C]GGTATGTATATTGGG | 221178 |
rs547560217 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288926 | GTTCATGGCTTTAGG[C/T]CTACAAAAGCTGTAC | 221178 |
rs547561752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241427 | GCGCATTTGTGAGAC[A/G]GCATTACTCAGCGAA | 221178 |
rs547573742 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030988 | ATAATTGAATAACCG[G/T]TCAATTCTAGCTCTT | 221178 |
rs547585679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276343 | AAAGAAGGAAGTTCT[A/G]ACACTTGGTACACAT | 221178 |
rs547606489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995212 | AAAAAAAATTGCATG[G/T]TAAAATTATTTATCA | 221178 |
rs547613527 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986346 | AATGGGCCAGAGGAG[C/T]GTCAGGAGACCTGGG | 221178 |
rs547624153 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138867 | AAAGTGCTGGGAACA[C/T]AGGCATGAGACACCA | 221178 |
rs547625060 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291707 | GGCTTCTCCTGAACA[A/G]CAAGCAACAAAATAC | 221178 |
rs547634885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272995 | AGAGCTGTCAGGGAG[C/T]GGCAGAGCAGAGGAG | 221178 |
rs547640365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126566 | GAGAGAGACAGACTC[C/G]CAGGGCGCAGGACAG | 221178 |
rs547658642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000803 | GAGCTGTGGGTCAGA[A/G]GTTTGAATTCGGGAG | 221178 |
rs547668106 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24140522 | AGGGTCACGTGCAGA[A/G]GCAGAGCTGTTTGGA | 221178 |
rs547668747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162298 | TTTCTTCCCTTTGCC[C/T]TACTTCTCCCTGGCA | 221178 |
rs547670757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139531 | TTATTACCATCTGTT[A/G]TATTAAGGTGCTGCA | 221178 |
rs547680106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187896 | GTGAAAGGAAGAGTC[A/G]CCCATCTCTATTTTA | 221178 |
rs547681860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087143 | CCTCATACTCCCATC[C/G]CAAAAGATCACAGGG | 221178 |
rs547687221 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133091 | TTAGCAATGGATTCC[C/G]ACGTATTTCCAGCGG | 221178 |
rs547696402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229599 | TTTTTAAGACAGGGA[C/T]GTTAAGGTCGGTTCT | 221178 |
rs547707887 | snp | C/T | 0.00652921 | 0.0567624 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025813 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 221178 |
rs547721954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214396 | TTTACATGTTACCAA[A/G]AAAGGTGTCACGCCA | 221178 |
rs547722578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274142 | CACATTGGCTAACGC[A/G]GAGGTTTCCAGCCAA | 221178 |
rs547727124 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168735 | AACATCCCTCCAGCC[C/T]TCATTCAAAACAAGA | 221178 |
rs547731092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106127 | CAGCCTTGAGCTCCT[A/G]GACTCTTGCAACCCT | 221178 |
rs547732393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133991 | GAGCCCCTGGGGGAA[A/G]GCTCTTTCTGCATGC | 221178 |
rs547738485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263521 | AAGGCTGTGCAAAAG[A/T]CCCTGATATAAAATG | 221178 |
rs547746257 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172096 | TCCTGCTTGTCCATG[A/C]ACACTCACTAAAGCC | 221178 |
rs547757570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065694 | ATTAATACTAGAATC[A/G]CATGGTATTGTATTT | 221178 |
rs547775149 | snp | A/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158741 | TAGTAAGAGTCTTAC[A/G]TGGGCTAAAGTTTTA | 221178 |
rs547794985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100757 | GATTTTGCTCTTACC[C/T]GAGCTCCTCACTCCC | 221178 |
rs547799018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253040 | TTATAATAAGGAGTT[A/C]ACTTATTAGGAGTTA | 221178 |
rs547799997 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306509 | GGTGAAACTACTAGC[A/C]GACCCAGCTTTCCCA | 221178 |
rs547803208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060281 | AGAAATACTTACAAC[C/G]TGCACACTTACTATC | 221178 |
rs547806900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070347 | CTTGCCTCCTCTGCC[A/G]CCCCCCTACCATATG | 221178 |
rs547807445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294153 | GCGGGGCCCTCCTGG[A/G]GAGAACATTTTAGCT | 221178 |
rs547813195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279262 | GGCACACGGAGCAGC[A/G]GCCCTGGGCAAGGAG | 221178 |
rs547818173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137686 | ACTGCTTGAGCCTGG[A/G]GGGCGGAGGTTGCAG | 221178 |
rs547847326 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24297219 | AATTTTTAAAATTTT[A/G]TGTGGAGATGGGGTC | 221178 |
rs547848386 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193149 | AGGACCTTCAGGAAG[C/G]TTTGTCTGGCATGTG | 221178 |
rs547848632 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24306581 | TTTTCAGGATGCAAT[A/G]AAAGTGGATTTCAAA | 221178 |
rs547850029 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186374 | GGTCAGAGGTTTACG[A/T]TATGTCAGGGATACA | 221178 |
rs547850628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154226 | ACAAGAGTGTGATTT[G/T]TTTTCCACTAAAAGC | 221178 |
rs547864032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082549 | TCTTTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 221178 |
rs547866021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148795 | AGCAATGAGTGTGTG[C/T]CCAGAGAGATCTGGA | 221178 |
rs547868665 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046890 | AGTTCACTGAGACAG[C/T]GGTATTGCAGTAGAG | 221178 |
rs547869421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030035 | GTTCTCATATATGCC[C/T]TACCTTCTCCTAACA | 221178 |
rs547898215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988242 | GTGAGCCACTGCGCC[C/T]AGCCAATTTTGTTCC | 221178 |
rs547900759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001585 | TGAATGCCCCTGTGT[C/T]CTGATGGTGATGCTT | 221178 |
rs547911303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076235 | ACTGCCACAGGTGCA[G/T]TTCTTAAAAGTTGAT | 221178 |
rs547914031 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153862 | GGGGTTGGAATCCTA[C/G]CCCAGCCACTTCTAA | 221178 |
rs547918217 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238761 | GAGAATACCTTGTAC[A/C]TTTGGCTTTGTACTT | 221178 |
rs547920553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277167 | AGTTCACCTTGGGCC[A/G]GGCGCGGTGGCTTAC | 221178 |
rs547934436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109179 | TGTTCTCATTGTTCA[G/T]TTCCCACCTATGAGT | 221178 |
rs547953849 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139799 | CAGGCCGGGCGCGGT[A/G]GCTCACGTCTGTAAT | 221178 |
rs547960522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138976 | GTTATTTCCTAGGGC[G/T]GCTAAAACAAATTAT | 221178 |
rs547976350 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085421 | TGTGAGCCACCGCGT[C/G]CAGCTTCTGCCTGCT | 221178 |
rs547980997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237917 | ATGTTTAAATATGCA[A/C]TATATAAACATACAT | 221178 |
rs547982516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209190 | TCAGGAATTCGACTT[A/G]AACACAGATGTGATC | 221178 |
rs547983546 | in-del | -/T | 0.468813 | 0.120918 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148369 | TTTTGTTTTTTTATT[-/T]TTTTTTTCCTGAAAT | 221178 |
rs548011830 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087798 | GTTCTGGGTGGCCAC[A/G]GGGCTCCTGCTCCTC | 221178 |
rs548014164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283719 | GGTTTTAGTAATACT[G/T]TTGCCTTGCAGATAA | 221178 |
rs548016570 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24143438 | GTGTTGATAAAAATC[C/T]GCAGCTGCTGGCAGT | 221178 |
rs548028507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989096 | TTTGTGAGAAAGTTA[C/T]AAAAATTTCTAGTCT | 221178 |
rs548034272 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019713 | TAAAATAGGACTGCT[-/A]AAAAAAAAATGACAT | 221178 |
rs548041856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245219 | AGTTCCAAGTAGAAT[C/T]GCAACCAAACTACAT | 221178 |
rs548055437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144431 | CTCAGCACCTTCTGT[A/G]TTCCAGGAACTAGGC | 221178 |
rs548060875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989617 | CCCTCTGACCCACAG[A/C]GTAACGTCCCAGTTC | 221178 |
rs548065195 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294524 | AACATTTTTATTCCA[A/G]AGAATTCTGAATTGC | 221178 |
rs548079914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166541 | CACTATAGCCCCAAG[C/T]ACATCAGTCATGACT | 221178 |
rs548086694 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208469 | CAGTGAGTGAATATA[A/G]GTGGAGTCTGAGTTC | 221178 |
rs548089873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106623 | GTCTAAGTACTGACA[A/G]TTCGGTGATTGTTTG | 221178 |
rs548092149 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24220589 | TATCCAGTCTCATCG[A/C]AGAGATGATTCAAGC | 221178 |
rs548098431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053505 | GGATCTCAGCTTTCT[C/T]ACCTGGCTAGAAGTG | 221178 |
rs548119301 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139807 | GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 221178 |
rs548123576 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142775 | TCTTTTTCTTTCTCA[G/T]GCATTTGGTAGGTCA | 221178 |
rs548129518 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24144472 | CCAAAAAGTTTCCTA[A/T]TTAAGAAGCGTTGGA | 221178 |
rs548130077 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082713 | TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 221178 |
rs548132897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012653 | TCCCTCCCCGTCTTC[C/T]GCAGCCAACCCCCAA | 221178 |
rs548147733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251192 | GTGAGTTTGGGTAAG[C/T]AAGGCTTGCCTTCAG | 221178 |
rs548174666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006313 | CTCATCAGCAGGTAA[A/G]CACACAGGGCCTTCG | 221178 |
rs548177881 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225491 | CTCATCTGGGCTCCC[A/C]GAAGGGCCACAGCTC | 221178 |
rs548178554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292219 | TGTGTGGTTATACAT[G/T]AGGCATGTCACCCAT | 221178 |
rs548185583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104562 | AGACAAGAGCTCCTC[A/G]GAAAGAAGCCGATTC | 221178 |
rs548203078 | in-del | -/CA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24015748 | TGGCAGGCCCCCCCC[-/CA]ATTCCTAGGTCCACC | 221178 |
rs548205519 | snp | A/C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24188233 | GTAGTCCCAGCTACT[A/C/T]GGGAGGCTGAGGCAG | 221178 |
rs548206624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099439 | CTCAGTGGCCACATT[C/T]CAAGTCGTCAGTGGC | 221178 |
rs548222197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122261 | GCCTGATACCACACA[G/T]GATTACGATTTTGAA | 221178 |
rs548222828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988841 | GGGTTTTTCTCCCCC[C/T]TCTTCTTTATATTGG | 221178 |
rs548231135 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24051086 | ACCTCTTTCCTTCTC[C/T]GGATTTCCCCCACCT | 221178 |
rs548236141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024188 | TAAGGGAGGTGACCA[A/G]TCACACTGTGAACTG | 221178 |
rs548236875 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302990 | ACACAAAGCTTTATC[C/G]TACACAGAAACACCC | 221178 |
rs548238845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111930 | GGTATTGAGGTTATA[C/T]TGCCTCTGTCCAATC | 221178 |
rs548240664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232134 | CAGCCTGGAGAACCA[A/G]GAAGCCAGATGTGTA | 221178 |
rs548247935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105174 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCATGATC | 221178 |
rs548269567 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24101714 | GAATCACGCACCTAT[A/G]TAAGTGGAATTGTTC | 221178 |
rs548274834 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24299862 | CACCCAGTTCACACA[A/C]TGCACACGTACACTG | 221178 |
rs548299264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112369 | GTGCCACTCTGTAGT[A/G]CTCCCCACATTGTAT | 221178 |
rs548302073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196107 | CAGCAATTAACTTAC[C/T]GCAGAGTTTTCAAAA | 221178 |
rs548309549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996653 | CTGATTAAAAGAGTA[A/G]CTTACAGGAGGATGT | 221178 |
rs548331716 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061568 | ATTGTGTCTTTTATA[-/G]GGACATGGATGGAGC | 221178 |
rs548350641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133288 | TAAGTACTTAGCCCA[A/G]TGAGATTAAGTTCAT | 221178 |
rs548354991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296313 | GGAGTCAGGCTCTTT[G/T]GCCTCCAAAAAATAT | 221178 |
rs548358931 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189919 | ATATTACATAATATA[-/T]ATTATATAATTATAT | 221178 |
rs548360144 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158985 | CACTATAAAAAGTAT[C/T]GCATGTAAATGTTAA | 221178 |
rs548362773 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195442 | TTTGTGTGGGCACCT[C/G]TTTTCAGTTCTCTTG | 221178 |
rs548368835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281524 | CTGGGGCACAGGTGC[A/G]GACCCATGGGCCATG | 221178 |
rs548405568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281177 | GCCCAGAAGGCAAGA[A/C]CAAGGCTGTGGAGCG | 221178 |
rs548405842 | snp | A/G | 1.65307e-05 | 0.0028749 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24286829 | GTGAGGAGCAGGACG[A/G]GGAGGCCAGCCAGAG | 221178 |
rs548409402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194577 | AGTTTGAGGATTTGG[C/T]AGTCAGTGATCCTGC | 221178 |
rs548416181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053933 | GGAAGTGTTATTATG[A/G]GGTGTCTATGTGCTT | 221178 |
rs548424463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165962 | TGTGACTCTATAGCT[A/G]AAAGAAAAATAGCCT | 221178 |
rs548438640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121970 | ATCTATTCATCATTA[C/G]TTTAGAGTAGATAAC | 221178 |
rs548456260 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184864 | AAAGGCAGTGTAAAA[A/G]GAAAATCCATTGTTT | 221178 |
rs548458656 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24230761 | GAACTTCTGTACAGG[A/G]TGGCTGGGTGGAGAG | 221178 |
rs548465581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250794 | TTTTGTCTGAAGGTG[C/T]TCCGCTGTTGGGAAA | 221178 |
rs548487571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019939 | TTCTGTGGTTTTCAG[A/G]CCAGCCACACCTCTT | 221178 |
rs548502820 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062505 | GCTCCAGGGCTCTGT[C/G]AACCTGGGTCACCTC | 221178 |
rs548517546 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24122939 | ATGATCTTCAGCTAC[A/T]CTAAGAAGCGTGTCA | 221178 |
rs548531701 | in-del | -/AAAAAAAAAA | 0.0566069 | 0.158427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302460 | GTAAGACCCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 221178 |
rs548533998 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009795 | GTCTGTTGATGTTAA[C/G/T]TCTGGTCGGCTTTTT | 221178 |
rs548539630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101304 | GCACCATGAACATTC[A/G]CTATGTTGGATAAAC | 221178 |
rs548542715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047768 | ACCAATAGAATCTGT[A/G]TAGATATATGGAAAG | 221178 |
rs548544677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042183 | GTGGGTTGTGAGAGA[A/G]AAAGCAGGGTCCAGA | 221178 |
rs548570450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003884 | ACATCAGCAAATACA[A/G]AACCCATTAAACAAG | 221178 |
rs548578960 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24300795 | TTAGCCACAAGGTCA[C/T]GCACATCCCCAGTCT | 221178 |
rs548579598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134394 | ATCGAACAAGCCCCC[A/G]GCTGACTTCTTGCTG | 221178 |
rs548586791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296801 | CACATTTTTCTAGTA[A/G]GCAGGAAAAAAAAAA | 221178 |
rs548588959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177727 | AAAGTGTTGGGGTTA[C/T]AGGCATGAGCCTGGC | 221178 |
rs548617165 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24233803 | TCTAGCCAGAGTGAG[A/G]ACCCCCTGGGATGCA | 221178 |
rs548620058 | snp | A/G | 0.000109866 | 0.00741086 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300363 | CTGAAACATGTCCAC[A/G]TGTTCTGAATATATA | 221178 |
rs548630162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262165 | CATAGGAAGTGCTTA[C/T]GTTGTTTCAAATTTG | 221178 |
rs548650594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177054 | ACAGGCACGAGCTGC[C/T]GCACCCAGCCTGTAG | 221178 |
rs548651271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054703 | TTAATTTATGATGGT[G/T]CTTAACCAGTGTGTA | 221178 |
rs548652894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24214453 | ATTTTCTCTTTACAA[G/T]GCATGTGCTTCTCTA | 221178 |
rs548685464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24108463 | TGGGCTTTGAGGAGT[A/G]CAGCCCTAGGATGGG | 221178 |
rs548693169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144075 | GACTGTGAATGTTCA[C/T]GAGCTGAATGTGCAC | 221178 |
rs548694190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079521 | CAGATTGCTTTCAGA[A/G]TCTTGTCTAGAAGTT | 221178 |
rs548706718 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062709 | CTGAATAAGGGGTTG[C/T]GTGTGTGTATGTGTG | 221178 |
rs548715832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294566 | TCCCTTAATCTATGG[C/T]AGACTGTAGTCTATT | 221178 |
rs548739301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065784 | CCATAAATAGTTCTT[C/T]CGACAATGCTGTGAG | 221178 |
rs548743049 | snp | A/G | 8.94222e-05 | 0.00668604 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302556 | TTCTGGTTAACAAGC[A/G]ACCCTCAGTCCCTGT | 221178 |
rs548746626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109190 | TTCAGTTCCCACCTA[C/T]GAGTGAAAACATGCG | 221178 |
rs548763132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120292 | GAAACACTGCAGACT[A/G]TGAAAGACCCACGTC | 221178 |
rs548770835 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24068749 | TGGTGGTTTTGACTT[C/G]CATTTCTCTAATGAT | 221178 |
rs548805918 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275450 | CCCCAGTCAGAGAGG[A/C]GCTGATGGTCAGCAC | 221178 |
rs548820250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984286 | TGCCACAGAAGTTTC[A/G]GTATTCACCAGTCAT | 221178 |
rs548841613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277986 | AGGGACTTTAAAATC[A/G]TGAAAGTAGTTAGGG | 221178 |
rs548844374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140025 | AGTGAGCCAAGGTCG[C/T]GCCACTGCACGCCAG | 221178 |
rs548844750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280526 | CAACCACGGTTTAAA[C/T]TGATAAGGAAAAATG | 221178 |
rs548849191 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070593 | TTGACTGGGCCACAG[C/G/T]GTGCTGATATTTGGT | 221178 |
rs548849480 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24185106 | AGTTCGGGCATTTCC[C/G]CCGCTTTCTGTAGCT | 221178 |
rs548860711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060846 | GAGTTTGAAATCAGC[A/G]TGGCCAACATGGCAA | 221178 |
rs548867440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073885 | GGTGTGCCAGTTACG[C/T]AGACCAAGACATAAA | 221178 |
rs548876728 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24085545 | TGCAGAAATCAGCTC[A/G]AAGGAGGACGTCCGA | 221178 |
rs548885266 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24202698 | AAGAGAGTGAGAACT[A/G]TCTTATTAGATAGTT | 221178 |
rs548887595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153697 | CCATATGTATGAAGA[A/G]CACATACTTTATGTG | 221178 |
rs548895480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157707 | AAGGAGTTTCCTTTC[C/T]GCCCTGTACCTCTTG | 221178 |
rs548913139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244444 | TTCACTGTGGTTTCA[A/G]AAAACATTTTAAAAT | 221178 |
rs548913780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130966 | TACACAGGGGTGGAG[C/T]GGGGGACGCTTTCTG | 221178 |
rs548930194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277398 | GCAGTGACCCGAGAT[C/T]GCGCCATTGCACTCC | 221178 |
rs548959225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119947 | TTTTCCATGAGGGAG[A/C]AAATGCAGAAGTTTT | 221178 |
rs548968748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24282715 | CAGCCCTCATCGTGC[C/G]GGACACCATCACCAC | 221178 |
rs548976967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131453 | CGCCTTATCTTGTTT[A/G]CCTCAGAATCCTCCA | 221178 |
rs548979968 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24139863 | ACGAGGTCAGGAGAT[C/G]TAGACCATCCTGCCT | 221178 |
rs548980529 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24248573 | GGTCAGTTGTGACTT[A/G]TCCCAGCTCACACCA | 221178 |
rs548981025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051506 | GACATACTCATGCAC[A/T]CCCAACCCTTAGGGG | 221178 |
rs548983924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037980 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 221178 |
rs548986502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168916 | ATTCTTTAAATGGTA[G/T]GTTTTACCATCTACC | 221178 |
rs548988534 | in-del | -/T | 0.420407 | 0.182924 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183607 | GAGATTTCTTTACAT[-/T]TTTTTTTTTTTTTTA | 221178 |
rs548998138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079600 | TAATACAGGGGGGTC[C/T]TGACGGCTTGAGGGA | 221178 |
rs548999174 | in-del | -/TATAT | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181413 | AGCTTAAAACACAAA[-/TATAT]TATACAGCTGTACAA | 221178 |
rs549007980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181188 | GTGAGGAATGAATGC[A/G]AAGGCCTAGGACATT | 221178 |
rs549026324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039674 | GACTGGAGGGGTCCA[C/T]AGGTTGTGAGTTTCT | 221178 |
rs549029548 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24259256 | AACAGATCAGTGCAT[A/C]TTTCTGCTGCTGTCT | 221178 |
rs549041290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155693 | TGTGGTAAAATACAC[A/G]TAAGACTTACCATTT | 221178 |
rs549046037 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242693 | TGTAACATGTTATTC[C/T]TTTGGCGTTAAAAAT | 221178 |
rs549046914 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221806 | AATTCTTACCTCTGA[A/G]TTTTTTTTTTTTTTT | 221178 |
rs549048083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174255 | TGTGTAGAGTTGCTC[A/G]TATTATCAGTCTTTT | 221178 |
rs549051711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137627 | TAGGCAAGCGTGGTA[C/T]GCATGCCTCTAATCC | 221178 |
rs549053456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998874 | TTTCATTAAAAATCA[A/G]TTGGCTTTATATTTG | 221178 |
rs549067545 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984276 | CAGAGTCTTCTGCCA[C/G]AGAAGTTTCGGTATT | 221178 |
rs549085331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167467 | AACAGAGAACACGGG[A/G]CCCACAGGCCAGCCT | 221178 |
rs549090340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992530 | GGCTAATGAAGGCTT[C/T]GTATCTTTGATGTGT | 221178 |
rs549094950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146186 | TAGAGGGAGTCTCAG[C/T]CAACAGACTTTGAGT | 221178 |
rs549098966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073262 | AAAATTTCTAGGTTT[A/G]TGAATCCCACTACCC | 221178 |
rs549103584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126480 | AATTGTGTCTATTCT[A/G]GAGTTTCCCTGGCAA | 221178 |
rs549104383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161381 | GTGGCTGGTGCCTCC[C/G]GGGACCCGGAGCGAT | 221178 |
rs549119948 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24117189 | ATAACAACTGTACCT[A/G]CATTGTAGATGGAAT | 221178 |
rs549121270 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054537 | TGTGCAAACCAGATA[C/T]GCATTTTTAGTTTAA | 221178 |
rs549126783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201804 | AATGTATTTACCATT[A/G]TGATGTTGTACAAAT | 221178 |
rs549146505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041171 | TTGATTCAACCCACA[A/G]TAGCTCAGAACCACA | 221178 |
rs549148603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996151 | ACCTAATGGGATTAT[C/T]ATCTCATATTTCAGG | 221178 |
rs549156249 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146699 | AGAGATATGTGAATG[C/T]CATGATTATGTTATA | 221178 |
rs549169605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247029 | GTTTGGGTGTGGATT[C/T]CCCTCTTTACCCTGG | 221178 |
rs549182349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141610 | CAGTCCCTGTGATAA[C/G]ATGAGTACTTCATGA | 221178 |
rs549183188 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100265 | AAGTGGCACCTATAT[G/T]GCCGCACTGCATTGA | 221178 |
rs549193449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257295 | GTGGGAACTTCACAG[A/C]GACAAGCAAAGGACG | 221178 |
rs549194624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186210 | TGTTACGGTTCACAG[A/G]GGAACCTAAAGAAGA | 221178 |
rs549222163 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24000323 | GATACAAAGATAGAA[A/C]AGGTTTCAAAGGGAG | 221178 |
rs549227292 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064899 | AAACATCAGACAAAC[A/C]CAAATTGAAGAAAAT | 221178 |
rs549229629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156263 | GGAATTGCCATACCT[G/T]TTGTCCACAGCAACT | 221178 |
rs549233054 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251254 | GCCAGGCTCTGTGTC[A/G]GTGGGGAGGAGTAAA | 221178 |
rs549234459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041770 | CAGGAGAAGGTCACA[C/T]ACAAGCCATGTCTAG | 221178 |
rs549236914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293558 | AATAAAAATTAGTTG[A/G]CATGACAGAAAGTCC | 221178 |
rs549239561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272528 | GAGAGCTCTGAGAGG[G/T]CAGGGGGCAGGGGAG | 221178 |
rs549243590 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136991 | CCCGCCACTACGCCC[A/G]GCTAATTTTTTTGTA | 221178 |
rs549254592 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24028660 | TTTTGGAAAATTCTA[A/G]TTGCCTCTCTTTTAT | 221178 |
rs549259097 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147824 | CTTGACCGCTCTAGA[C/T]ACCTCATATCAGTGG | 221178 |
rs549266162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098066 | AAATGGCCCTAGAAG[A/G]CTATTAAAGACCAGG | 221178 |
rs549270937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234191 | CATCTTATTAATGCT[A/G]TGCATGTTAAGCTTC | 221178 |
rs549273686 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24152138 | ACAGCAGATATTTAT[C/T]TTCCCACAGTTTTAG | 221178 |
rs549279639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264226 | GAGTTAAAAAGTAAA[A/C]GTTATTGAAAATATC | 221178 |
rs549287318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063170 | CCAGGTCTGCCCCAC[A/G]TGAGGGTGAGCTCCA | 221178 |
rs549310516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121400 | TCTTTTTATAAACAG[C/T]AAACATTTTGCTATT | 221178 |
rs549322361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080317 | ACAGCAAGTGGGAAC[A/G]TTCCCTGCTATGGAA | 221178 |
rs549324143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063664 | GGGGCGGCTCCTTCT[C/T]CCACATCCTCTTCAG | 221178 |
rs549335969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241221 | TTTACCTACAAGCCA[C/T]AGAAAGAGTAACCCA | 221178 |
rs549338679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275589 | TGGGGTTTTAAAACT[G/T]ATTTCAATTTGGAGC | 221178 |
rs549340459 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980279 | GTTGCACAAAGCCAG[A/C]CTGGCGGTCGCGTTG | 221178 |
rs549343443 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24284463 | GTCAAGAGTTTAAGA[A/C]CCGCCTGGCCAACAT | 221178 |
rs549358197 | in-del | -/CACA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030067 | ACACACACACACACG[-/CACA]CACACACACACACAC | 221178 |
rs549375186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280662 | AGCATCAGGATATCT[C/T]GGCCAGTAAGCAGCA | 221178 |
rs549377569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981272 | GCCATATACCATAGG[A/G]AAAAAAAAATGTCAA | 221178 |
rs549388272 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075394 | GAATAAGCCTGGGCA[A/G]CAGAAAGTCTTGTAA | 221178 |
rs549395929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240555 | TTTGTCACCGTCATG[C/T]GGAGTTCATTCCTTT | 221178 |
rs549397794 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174599 | ATCACTTTTTTGAGA[C/T]GAAGTCTTGCTCTGT | 221178 |
rs549407285 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24003472 | TAAGGCTGCTGTGCC[A/G]CAAAGCAAGTAATGC | 221178 |
rs549415474 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160362 | GTGATTCTCCTGCCT[G/T]AGCCTCCTGAGTAGC | 221178 |
rs549419758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007198 | CCTGGTGGCCCTGAG[G/T]CTCTGAGCCCTCTGC | 221178 |
rs549465051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993142 | GCAATGAACCTGCTG[C/T]GGCGAAGGTCGTGGA | 221178 |
rs549488446 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086520 | ATATGAAAGAAAGGA[C/T]GAATTCAAAAGACAA | 221178 |
rs549505752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065114 | AATCTTTATAACTTA[C/T]GGTAGCAAAACTCTA | 221178 |
rs549509191 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080809 | ATTACTGTATGCCTC[A/G]TGGGCTGTTCTTTAA | 221178 |
rs549514537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047120 | GAGTCCACCTCAAGG[C/T]GGGGTCCACAGGACT | 221178 |
rs549521358 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24178346 | ACTGCATTATGATAC[A/G]GCTGCAAGGAATGAG | 221178 |
rs549522057 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24020462 | TCACAATCCATTTGA[G/T]TTGGAAACCATTCTT | 221178 |
rs549530990 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24060552 | ACAAAGATGCCAAAA[A/G]CAATTGCAACAAAAG | 221178 |
rs549550656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24170516 | CGTCAGCAAGAGGTG[C/T]TACTTTCTATTTCTA | 221178 |
rs549551805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086978 | AGTGAATCTGGTTTC[C/T]CTGTGGCCCAAAGTA | 221178 |
rs549552490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115452 | GGCATTAGATTCTCA[C/T]AGGAGCGTGAACCCT | 221178 |
rs549561714 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115261 | ATGGCAGCAGTGACT[C/T]TAGCCATGTCCATGA | 221178 |
rs549566883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292903 | TGGGAGGCTGAGGCA[C/T]GAAAATCGCTTGAAC | 221178 |
rs549567339 | snp | C/T | | | intron-variant, nc-transcript-variant | SPATA13, MIR2276 | GRCh38.p7 | 13:24162432 | TGTTCTTCCAGTCCG[C/T]CCTCTGTCACCTTGC | 221178 |
rs549568401 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24264067 | GTTTCATGCCTCATT[A/G]TTGCCTATCATCGAG | 221178 |
rs549572087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005001 | TGAAAATGAATCTAC[A/G]TTCCCTTTTACATGG | 221178 |
rs549590316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074663 | ACCCTTGTAGGAATT[A/G]GGGAACTTGCTCAAA | 221178 |
rs549601605 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23991994 | TGGCACTGCCATTGT[A/T]GAGTGGTTACTACAA | 221178 |
rs549603016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24213105 | TGCACGGAGAAGTTG[A/G]AGGAGGAAGATGGTC | 221178 |
rs549609854 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036927 | ACTACAGGCGTGCAC[C/T]ACCATGCCCAGCTAA | 221178 |
rs549621687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036142 | AGTTTCAAAAATACA[G/T]ATTCACTTTAAAAGC | 221178 |
rs549637050 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24182352 | AAGAAAAGAGGTTAA[A/G]TTGGCTCACGGTTCT | 221178 |
rs549640715 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142818 | AGGCATTTGGAATCA[C/T]AATTCATGGGCCAGG | 221178 |
rs549646620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993747 | TGCTTTTTAAGGGGA[A/T]CTCTAGGTACTTTCC | 221178 |
rs549647458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285167 | AAAATCACCTGCTCC[C/T]GTGGCCAGGGGATGG | 221178 |
rs549651524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069219 | GCTTTGAGCAGTATG[A/G]CCATTTTTACAATGT | 221178 |
rs549658440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178336 | AATGTATTGAACTGC[A/G]TTATGATACGGCTGC | 221178 |
rs549660237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298582 | TGTTGAATGGAAGTC[A/C]GGGAGCCACAGTGAA | 221178 |
rs549667221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099191 | TGAATAGTGGAGAAA[A/G]GCATGCATTTATCCT | 221178 |
rs549683653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017250 | ACTCAGTTAATGCTC[A/G]CAATTCTCTTATCCT | 221178 |
rs549697278 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136923 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 221178 |
rs549702506 | snp | C/T | 0.00020031 | 0.0100058 | missense, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24249610 | CTGACTACGGCCAGC[C/T]GGCCAGCCGCAGTTT | 221178 |
rs549704357 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24164511 | GATGAGATGGGTGAT[C/G]AGGTACCATCCTGGG | 221178 |
rs549715653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153136 | TACTCTGATTTTATC[A/G]TCTGCATCTCCCCAT | 221178 |
rs549718410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260027 | TGTCCCTATTATAAA[C/T]GAGGCACAGTACCAG | 221178 |
rs549721252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110825 | CCAACTTGAGATAAG[A/G]AAGTTAAGAATAAAC | 221178 |
rs549722337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011334 | CGGCTTGGCCATCTC[A/T]TGCTGTCTCACGTTC | 221178 |
rs549733761 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987651 | AAAGTTTGGTGTTTT[A/G]TTTACCATTTTTAAG | 221178 |
rs549740091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023200 | GTTTTCTGTCTTTGT[G/T]ATAGGTTGCTCAGAA | 221178 |
rs549748573 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158353 | AAAGCCACTGCGGGA[G/T]ACCTAGGCTTTTACA | 221178 |
rs549765979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073925 | TTGGAGATGTGCAGC[C/T]TTGCACACCACAATA | 221178 |
rs549766840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981352 | ACTTCTATTTTACAA[A/G]TTATGTTATTTGTTT | 221178 |
rs549776013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230390 | GGAGCCCCAAAGGCG[A/G]CAGAATGAAGAACTC | 221178 |
rs549778873 | snp | A/G | | | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24302906 | GATCAATGAAGGAGA[A/G]AAGGTCTTGGAATCA | 221178 |
rs549798247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040304 | TGTCTCACAAACCTG[A/G]TTTTTCAAATCAGGA | 221178 |
rs549805885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244498 | TATATTGGCTTTTTA[C/T]TTTTGCAGAGTAAAA | 221178 |
rs549807397 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24273694 | ACTATAATGTAAATG[C/T]GATACATATTTTAAA | 221178 |
rs549809899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109332 | CATGGTGGATATGTG[C/T]CACATTTTCTTAATC | 221178 |
rs549810064 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24184629 | GCTGGGCAACAGCAT[C/G]AACTCACTAATCACA | 221178 |
rs549827051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121422 | TTTGCTATTTTATAC[A/G]TAGGCTAGCAGGCTT | 221178 |
rs549827612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277221 | AGGCCGAGGCGGGCG[A/G]ATCACAAGGTCAGGA | 221178 |
rs549835119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24035027 | AAAGCTCTACATGAC[A/G]CATCAACTTTCATTT | 221178 |
rs549850274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132440 | GTTTCAGTCCTGGCT[C/T]TGTCCTGGCTGTCCT | 221178 |
rs549852394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216027 | TGTAGGAAGTCAAGA[C/T]GCAGGGCAGTCTTCA | 221178 |
rs549852682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250025 | AAACTAACCACCTGA[C/T]GTTTGGATGCCTTTT | 221178 |
rs549866929 | in-del | -/CAAAAA | 0.00478085 | 0.0486577 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303903 | CAGCGAGACTGTCTC[-/CAAAAA]CAAAAACAAAAACAA | 221178 |
rs549867381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028697 | TACTATCTTTGTATA[A/G]AATTCCAATTGAATG | 221178 |
rs549872771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093335 | CTTTTCCAGGCACCA[A/G]TATCCCACTGTTCTG | 221178 |
rs549873380 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24200132 | CAACGGGCATTTTCT[A/T]AATTTAACCCAACTA | 221178 |
rs549883642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291176 | TGTTGCTTACCTGTA[C/T]TTTATAAACATGTCT | 221178 |
rs549888405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121858 | CCCCTAAGGTACCTC[C/T]CATCCCCCTCGATCC | 221178 |
rs549892180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147133 | TTTTTTCTTACCATC[A/G]AGAATGGAATGCTTT | 221178 |
rs549896242 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205557 | TAAATTACCATTAAC[A/T]TTCTTCACAGAATTA | 221178 |
rs549898577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235581 | CCTGGACAGCATAGT[C/G]AGACCTTGTCTCTTA | 221178 |
rs549905892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295205 | AGTATGGGGGACTCT[C/G]GAGTCCCTGCCCACA | 221178 |
rs549919537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222650 | GGGATGTATATTTGC[A/G]TCTTTCCTTCAACTT | 221178 |
rs549922930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035819 | TGGAGTTTGAGACCA[C/G]CCTGGCTAACATGGC | 221178 |
rs549948299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267116 | TAGTAGTGGCTTCTT[C/G]CAAAACTATCTTAGA | 221178 |
rs549953563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142205 | GCCAATATTAACATC[G/T]GACATAACCACAGTG | 221178 |
rs549959584 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24142369 | AGTCAGTTGTCAAAC[C/T]AAACTGTTTTCTCCA | 221178 |
rs549960332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235143 | AGACCAGTTAAACTT[C/T]GCAAATTATGTACTT | 221178 |
rs549970818 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307265 | CTCCGAGGGCAACCT[C/T]GGAGGGCACCCTGGC | 221178 |
rs549974932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044335 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 221178 |
rs549985030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274170 | CAATGCAATCAGAAT[C/G]CATTGCCTGCAACTT | 221178 |
rs549991263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005570 | ACAGCTTTCTTCCCT[A/G]GTAAAGGGATGAACT | 221178 |
rs549994680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037333 | GTTGTGCACATGTAC[C/T]CTAGAACTTAAAGTA | 221178 |
rs550014304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24296128 | GGTTTTTAACTGAAA[C/T]AGGCTATAGGTGGTG | 221178 |
rs550015501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048690 | CAAAATTAAAAAAAA[C/G]ATAAATAAATTGTAT | 221178 |
rs550022439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24063708 | GGAGGGGGCAGCCTT[C/T]TCGTTGCTGATGTTT | 221178 |
rs550029860 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131590 | AAGACATTTCAGTGG[C/T]TTATGAGAACAACAG | 221178 |
rs550031644 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216722 | AATAACTTCATCTCT[A/G]AAATTAGGACCTTGG | 221178 |
rs550051636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143454 | GCAGCTGCTGGCAGT[A/G]CTCTCATTCCTATGT | 221178 |
rs550052913 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295570 | TGAGCCGTGATCGTG[A/C]CCCTGCACTCTAGTC | 221178 |
rs550078287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012968 | TCCAGCAGGCCAGCC[C/T]GACACCTTCTCACCG | 221178 |
rs550097189 | snp | A/G | 0.000188608 | 0.00970919 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223178 | CAGTCGGAAGAGGAC[A/G]GGTGCCCACCCCGAG | 221178 |
rs550103082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24267967 | TCTGATTCTGCAGAC[C/T]TGGGGCAGGGCCCAG | 221178 |
rs550113364 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24284866 | ACTGATCTAAGAAGC[A/G]GACATTATGGTTATT | 221178 |
rs550114767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020766 | TAAATAATTTGGGCC[A/G]GGCGAGATGACTCAT | 221178 |
rs550120871 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148657 | TGGTTGAAGAGTTGA[C/G]AATCTCTGCAAGGAA | 221178 |
rs550135849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046225 | AAATCCTCCTCCTGT[C/T]ACCTCCTAGTCAATT | 221178 |
rs550146893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059035 | GGAGTGCAGTGGCGG[A/G]ATCTCCACTCACTAC | 221178 |
rs550157004 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24216623 | AGGTACCAGATCAAA[A/G]GGTAAGGGGGCTTCT | 221178 |
rs550168204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226939 | TATTGTCTGTTACCT[A/G]AGGTTCCCGTGGAGA | 221178 |
rs550177218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301239 | TTTACCCCATGAAAT[A/G]TATCTCTTTTGGTAT | 221178 |
rs550186075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070431 | AGATATCTCTTTCCA[A/G]AAGTCCATGTACTTG | 221178 |
rs550191691 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24002877 | CTCATTGGTCATCCC[C/T]GGGTGATTGGGCCCT | 221178 |
rs550194183 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119757 | TTCAGGATTCCTGCA[A/G]TAGCTGCCAAGGAAG | 221178 |
rs550199697 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154921 | GGAGTGCAATAGCAT[A/G]ATCTTGGCTCAGTGC | 221178 |
rs550202871 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258422 | CTGTAATCCCAGCAC[G/T]TTGGGAGGCTGAGGT | 221178 |
rs550211716 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24062430 | TGAAATTCTTCTCCA[A/G]TGGCGCCAGGGTGCA | 221178 |
rs550216983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209691 | ACTTAGGTCAATTGC[A/G]TATCTTGGCTACTGT | 221178 |
rs550225504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122882 | TAAAACAGTAGGAAC[A/G]ACCTGTAAGCAGATT | 221178 |
rs550228706 | in-del | -/CCTCCCTT | 0.200801 | 0.245111 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278989 | CTCCCTCCCTCCCTC[-/CCTCCCTT]CCTTCCTTCCTTCCC | 221178 |
rs550228965 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248156 | GCAGCCCTCCTCTCT[G/T]GCCAGGCTTTGAGGG | 221178 |
rs550232510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187987 | TCAAAGCTTGGCCTC[C/T]TGTGCCACATGGTTA | 221178 |
rs550238071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087628 | ACTCAGGCATTACAG[A/G]AATGAAGATGGAATT | 221178 |
rs550243477 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24289368 | GTTAATCTTGTCTAA[A/C]TGTCCCAAATTCATT | 221178 |
rs550244813 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24241818 | GCACTTTGAGAGGCC[A/G]AGGCGGGAGGACTGC | 221178 |
rs550260522 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047107 | GTCCTGGTGCACTGA[C/G]TCCACCTCAAGGCGG | 221178 |
rs550267502 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264793 | AATCCACGTGTGCTT[A/G]CAGAGAACAGGAAAA | 221178 |
rs550276878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115871 | CTGGCAGGCAGCCTC[A/G]GCTCCTCACCTCATG | 221178 |
rs550283013 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157356 | CAGGCTGGAGTGCAG[G/T]GGCGCGATCGCGGCT | 221178 |
rs550285586 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304845 | CTGTGGCATGTGTGG[A/G]GGTGTGTGTGTGTAT | 221178 |
rs550285697 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24260671 | AATTCTATCAAATTA[A/G]GTGAGAATTGACAGC | 221178 |
rs550289084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24081528 | TAAAAAAAAAAGCTG[A/G]CCCAGTGTGATGACT | 221178 |
rs550291886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048777 | AGCAAAGGAGAAGTC[A/C]AGGCTGAAATTCCAA | 221178 |
rs550292713 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232766 | GCTCCCCAGGCTGGT[C/T]TCGAGCTCCTGAGCT | 221178 |
rs550296878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123394 | CTCTCATGTAGCCTA[A/G]TTCACTGCTGAAGAG | 221178 |
rs550319680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191752 | CCTGACCTTGTGATC[C/T]GCCCGCCTCAGTCTC | 221178 |
rs550320898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006022 | TCCCCTGAGAAGGCC[A/C]GGGTCAGACTGGCTG | 221178 |
rs550326866 | snp | C/T | | | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269979 | CTCCTGCGTCATCCT[C/T]CTGAGTAGTTGGGAT | 221178 |
rs550327222 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23994575 | TGTTGGGTAGGTCCC[A/G]CTAATTATCCACAAC | 221178 |
rs550336182 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24156745 | GGGACTTTACATACA[G/T]TATTACACTTAATTT | 221178 |
rs550346755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281340 | AAAACTGGGGATGGG[C/T]CCAGGCAGGGGAGTG | 221178 |
rs550347292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242596 | TCGTAAAATGGGGGT[A/G]ATTACGTCTTCTTTG | 221178 |
rs550349170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007609 | TTATAGGTGGCACCA[C/T]CACACCTGGATAATT | 221178 |
rs550350830 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114096 | GAGGTGCAAGACATT[C/T]ATATGCAGTGTAGAA | 221178 |
rs550352812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075470 | TTTTCATTAAGCCAA[G/T]GGTTTAAATAAACTC | 221178 |
rs550362574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279456 | GCAGCTATGGCCTGC[C/T]GGGGGCAGGGGTGGC | 221178 |
rs550363627 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24103382 | CTCAGCACTTGAAGA[G/T]ACTGAGGTGGGAGGA | 221178 |
rs550367942 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203971 | GGTCTAGTGAGGGTG[A/C]CTCAGTCATGCAAAA | 221178 |
rs550393450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163596 | TCTTTTTTAGTCTTT[A/G]TCTTCCTAAGAGTTG | 221178 |
rs550405232 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247361 | TGCCACTGATTAACT[G/T]TGTGGCCCTGGGCAA | 221178 |
rs550407424 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095635 | ACCTTAGATAACAGT[-/A]AAAATGAGACTGGGT | 221178 |
rs550415980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076211 | TGTACATGCTTTTAT[C/T]ATTTAAGAACTGCCA | 221178 |
rs550428943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118574 | AGATGACTTAAGCCC[C/T]ACCCCCTGAATTTCT | 221178 |
rs550439091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154594 | TTTTCATGTTGTATT[A/C]GTTTTCTATGATGTG | 221178 |
rs550439286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149336 | GGCATCGTTTGTCAT[C/T]CTCTTTATGTTCTCA | 221178 |
rs550469551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196855 | AGTACATTTCAAGAG[A/G]TAAGGAGAAGCATGA | 221178 |
rs550478386 | snp | G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979298 | GAGTGTGTGTGTGTG[G/T]GTGTGTGTGTCCTTG | 221178 |
rs550496249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239984 | ACTTTAAACTGTCTC[C/T]TTACTCTTAATTAGT | 221178 |
rs550509475 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24128255 | CATTGTCCTTGTGCC[C/T]GGAGGGGTGACCTAC | 221178 |
rs550512925 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24245093 | GAGGACATGGCTATG[C/G]CCAGCTGCATGTTTC | 221178 |
rs550514530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281957 | TGCTTGGCAAGGAAG[A/G]CCTAAAATGCTGGTG | 221178 |
rs550529952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178863 | GTCATGCACTCATCA[A/G]TTACCATAGTCAATT | 221178 |
rs550551924 | snp | C/T | 0.000821524 | 0.0202506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086526 | AAGAAAGGATGAATT[C/T]AAAAGACAAGTTCGA | 221178 |
rs550559416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246553 | CTGTGTGTGAGAGAC[A/G]GAGTTCATAGAAAAA | 221178 |
rs550562361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220172 | TGTTGGTACCTCTTC[A/C]TCTGTAGACAGCACT | 221178 |
rs550562869 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24074721 | AAAAACTTCAGACAA[C/T]TGGATTTAGCAGAGT | 221178 |
rs550574422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298690 | CCCTCCCCATCCTTG[A/C]CCACTGCCATGAGGA | 221178 |
rs550579636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141007 | AGGTGAAACCCTGTC[C/T]CTACTAAAAATACAA | 221178 |
rs550588465 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23993468 | ACGGCAATAAGGCTT[C/G]TCTGCAAATAAGAGA | 221178 |
rs550594533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991092 | ACTGTCCTGGCAGAG[C/T]CCCAGGCAGGGCGGC | 221178 |
rs550597335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24264294 | AAAGAAGAAGAAAGA[A/C]TATTAAAAGTCAGAG | 221178 |
rs550598412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24287382 | TGCCGAGGCTGGTCA[C/T]GAACTCATGGACTGA | 221178 |
rs550617027 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304069 | GCAATGAAGTCACAA[A/G]GACAGCCAAAGCAGT | 221178 |
rs550620320 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979344 | GGAAGAAATTGTGAA[C/T]AGGAATCCTGTATTT | 221178 |
rs550623379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049383 | ACGTGTGCAGGTTTG[C/T]TGCCTGGGAGCAATA | 221178 |
rs550626292 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24170686 | TGCCAATCAGTCTGG[C/T]GTAAAAAGATCATTA | 221178 |
rs550642220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272382 | CTGAGAGGGGCCTGG[G/T]TCAGTGCACTGCGGA | 221178 |
rs550702038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24067907 | TGGGGTTTCACCATG[C/T]TGGCAAGGTTGGTCT | 221178 |
rs550708224 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979670 | GGAAACGCGGCATTC[C/G]GACAGCCGTCCAGAG | 221178 |
rs550708467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062680 | AGTATCCTCATGACT[G/T]CACCTGAGCTGTACT | 221178 |
rs550738424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097057 | TCGAGGAGAAACAGC[A/G]TTGGCCCCGGCTGAA | 221178 |
rs550741459 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24150551 | ATAAATATTGATTGA[-/T]TTTTTTTTTTTAAGG | 221178 |
rs550744558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178225 | GGCGCAAACGTTCCA[A/G]TAATAACAGCTCCTA | 221178 |
rs550745267 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064907 | GACAAACCCAAATTG[A/G]AGAAAATTCTGTAAA | 221178 |
rs550749830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119050 | AGTTGGGCCTGCAGG[C/T]GCCTGCCACCGCTCC | 221178 |
rs550751423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154298 | TCTAATTGTCCATCA[A/G]CAATAGAATAGGACA | 221178 |
rs550768755 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277178 | GGCCGGGCGCGGTGG[C/T]TTACGCCTGTAATCC | 221178 |
rs550782665 | in-del | -/GGAT/TG | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024360 | AATGGATGGACGGAT[-/GGAT/TG]GGATGGATGGATGGA | 221178 |
rs550792060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085427 | CCACCGCGTCCAGCT[C/T]CTGCCTGCTTTTTAA | 221178 |
rs550804347 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189643 | AATATATATATTTAT[A/T]TATATATTATATATT | 221178 |
rs550807142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003267 | GTGTTGGATTAAGCC[A/T]TTTTGATGTTTCCAT | 221178 |
rs550807335 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24089669 | CCATGCGATATTTGA[A/G]TATAGTTGTCCTACA | 221178 |
rs550813194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24113657 | CAGGCAGATCACGAG[G/T]TCAGGAGATCCAGAC | 221178 |
rs550813762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263098 | AAAAAAAGAAAAGCC[A/G]TAGCAGGTGTTGAGG | 221178 |
rs550834564 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24303331 | TGTTCCCTGGCATCG[C/T]CTGTGTCCACACAGA | 221178 |
rs550836884 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24151876 | ACAGTACTAAGCAGT[A/G]TAGATGCTTGATTAA | 221178 |
rs550845212 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172480 | TTTTCTAAAACGTTC[A/G]TGGTTTTTCATTTTA | 221178 |
rs550855534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079730 | CTAGTGTGCAATTAT[A/G]TATCATTAGTTACAG | 221178 |
rs550881964 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24175105 | ATGTTCCCTGGGCAC[A/T]GGAAAAGAATGTGTA | 221178 |
rs550883009 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991790 | GACTCTGAGTTGGGG[C/G]CAGGTGGGCTGGGGT | 221178 |
rs550920225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24091702 | TGTAATCCCAGGTAC[A/T]AAGGAGGCTGAGGCA | 221178 |
rs550922757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204059 | TAATATAGTAATTGT[A/G]AGTGTCAGGAAGCCA | 221178 |
rs550930782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015307 | TACTGCAAAATAGAC[A/C]CATGACATTATTTAA | 221178 |
rs550941674 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068718 | GCCATTCTGACTGGC[A/G]TGAGATGGTATCTCA | 221178 |
rs550946110 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027584 | CCTTTCTTCTACATT[A/C]TTGGGTTTTTTGAGT | 221178 |
rs550967947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009150 | CCCACCTAAACTCTG[C/T]TCTGGTTCTTCCTGG | 221178 |
rs550970199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102638 | CACCACTAAGCCTGG[A/C]TATTTTTGTATTTTT | 221178 |
rs550972805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985715 | GTCGTAAATCATTGG[A/C]AAGTCCTAAAAGACT | 221178 |
rs550980423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24166038 | GTGCTCTTCTGTAAC[A/G]TATAAAAGTCTTTCT | 221178 |
rs550983936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290024 | TATCTGGGACATTGT[C/T]ACAGGCCTCCTTGTG | 221178 |
rs551009781 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24211743 | ACTGACGATGATGGC[C/G]TCTGCTGCCAGAACT | 221178 |
rs551015177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992334 | GTTGTTGTGAAAATT[A/G]TATAAAATAAGGCAT | 221178 |
rs551016778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295008 | CCATTAATGGTAAAT[A/G]TATTTCGAGGCATAC | 221178 |
rs551021093 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24196034 | TGTAACTTGATTTTT[A/G]TGCCTTAATTTGCAT | 221178 |
rs551025442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256786 | TACTGGGTGTGTTAT[C/T]TGGGATAATAGAGTT | 221178 |
rs551027295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119063 | GGCGCCTGCCACCGC[A/T]CCCTGCTAATTTTTT | 221178 |
rs551034188 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135973 | TTAAGTGAATCTTTT[A/G]ATCTCCTGGAAACAA | 221178 |
rs551045619 | snp | A/C/G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24116779 | TACCAGCCCCCCCCC[A/C/G/T]CCAATGTGCTGATGT | 221178 |
rs551062908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177859 | GGGGATAGGATTTCA[A/G]CATATGAATTTTTTT | 221178 |
rs551073891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039097 | TTGTTAGAAAATCTG[A/G]ATTGCTCCCTGATCT | 221178 |
rs551075541 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24239237 | AGGATTTCAGGAGAT[G/T]ATGGAGGAAATAGGG | 221178 |
rs551090516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119857 | TTCTCCGTCAGTCTA[C/T]GCATGCTAGGAGAAT | 221178 |
rs551107996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262347 | GTGGTTGTTAAAATC[C/T]TACTTCTAATTTGTT | 221178 |
rs551113246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021852 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCACCA | 221178 |
rs551113273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24256299 | ACAGTTAATGACAAT[A/G]TATTGTATAGTTCAA | 221178 |
rs551115448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015510 | CTCTGTTAGCAGTAA[C/T]TTAATAAAAAACCTG | 221178 |
rs551138897 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24263207 | TGCTTCTGCATTTTA[C/G]TCAAATCGATTTTCA | 221178 |
rs551147607 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24055305 | TCATCCTTTCATTGC[A/G]GGTACAGTGCATCGT | 221178 |
rs551151890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114357 | TAATTCAGTGTGCAC[A/G]TGTGTGCCTGCATGT | 221178 |
rs551160949 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224545 | TTCTGGTGAACATTG[A/G]TGTGGCAGCCGGCCC | 221178 |
rs551161808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033932 | ACAGAAAAGAAGAAG[A/G]CAATGGTGTTTTTCT | 221178 |
rs551176124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209336 | TTAATTTTAAAAGGT[C/T]AGCGTTTTTGTTGAA | 221178 |
rs551183904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085193 | AGCGGTGCAATCTGG[A/G]CTCACTGCAACCTCT | 221178 |
rs551194308 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044798 | AAGACAGGCACAGAA[G/T]GACAAATACTGCGTG | 221178 |
rs551202150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174654 | CAATCTTGGCTCACT[A/G]CAACCTCCGCCTCCC | 221178 |
rs551233170 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24100116 | CTTTCTCTATCAATG[A/G]TTTATTTTATAATTT | 221178 |
rs551258972 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120017 | ACCCCCACAGAGTGA[A/C]AAGAAACAATCACCA | 221178 |
rs551261204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125113 | TTTCTCTCCAACCCC[C/T]GGACCCATACCCTCT | 221178 |
rs551267957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300594 | GAACAGTAGAAGTTA[A/G]AACTCAAGGGCAGGT | 221178 |
rs551269228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24044922 | GCAGAGTGAAGAGAG[A/G]TTGGTCAGTGGGTAC | 221178 |
rs551286194 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039633 | TTGCTCTGGTTGTTC[C/T]TCCTTTTGTCTCTTG | 221178 |
rs551309651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136009 | TCACTTTCCTGAGCA[C/G]AATTAAGCTCTTGGT | 221178 |
rs551313774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141506 | CCTTGACTCCTCCAG[A/C]TGAGCTCTAATCCTT | 221178 |
rs551328720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237762 | TTGAGGCCAAGAGTC[G/T]GAGACCAGCCTGGGC | 221178 |
rs551331399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094951 | AACCCTTGTGTGCTA[C/T]TGGTGGGAATTTGTA | 221178 |
rs551336103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278405 | GTGCCTAGCACATTA[C/T]AGGCACCTGATAAAA | 221178 |
rs551360547 | in-del | -/TTTTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24058966 | GGTCTGTGTATTGTT[-/TTTTG]TTTTGTTTTGTTTTG | 221178 |
rs551362362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123551 | TTCTGTAAGAATCTG[C/G]TAACAAAATCCTATA | 221178 |
rs551368197 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102105 | TCCCACTAACAGCGC[A/G]TAGGGTTCCAATTTC | 221178 |
rs551373087 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278100 | GAAGGGTTAGTGAGG[A/G]AACGGAGGGCAGGAC | 221178 |
rs551377282 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24136997 | ACTACGCCCGGCTAA[-/T]TTTTTTGTATTTTTA | 221178 |
rs551385958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163244 | TCTAAAAAATAAAAA[C/T]AAGAAATCAGCTGGT | 221178 |
rs551391865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248812 | ATTCATTTCTTCTCC[C/T]GGCAGGTCTTTGGGG | 221178 |
rs551407477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24175055 | TTAAATTTGTTGAGG[A/T]TTGTATGGCCCGGGG | 221178 |
rs551428598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254121 | CACAAAAGCCATCCC[C/T]ATTTTCCGTGGGTGC | 221178 |
rs551430243 | in-del | -/GATC | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995273 | GAAAGACAAAGGTGT[-/GATC]TTTGAACACAGGTAA | 221178 |
rs551437048 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24064009 | GCCTCTGGAGCAAAC[A/G]TGCCCTGGATCTGCT | 221178 |
rs551453439 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24225009 | ATTCTTTCTGTTAAG[A/T]GACTATTACCTGTCC | 221178 |
rs551453673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192615 | GGTAGGCACTTGAGT[A/G]TTGAATGAAAACTCA | 221178 |
rs551468604 | in-del | -/AT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24242310 | TATGTCTACACACAC[-/AT]GGATGAATGGAGAAA | 221178 |
rs551473234 | in-del | -/ACAT | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237954 | ATATGCAATATATAA[-/ACAT]ACATGTTTAAATATG | 221178 |
rs551477978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247612 | CTCAGCCCCCCAAGT[A/G]GCTGGGATTACAGGC | 221178 |
rs551480379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234279 | ATTTTATCTTAATTA[A/G]CACCTCATTTTAATT | 221178 |
rs551486103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24161516 | AGGGAATGCATTGGC[A/G]GAGTTGGTTTGGTCC | 221178 |
rs551494347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076996 | CTTCCCTTTGATTCA[G/T]ATGTTGTTGAGGGGA | 221178 |
rs551497274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301030 | AATTCCCTGGGGAAG[C/G]TGTTCAAAAATGCTG | 221178 |
rs551498799 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24024779 | GCTATATTTGCCTGC[C/T]GGGTGCAGTGGCACA | 221178 |
rs551506164 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051444 | CCTGCCAGGCTCTCG[A/C]CTCCAGTTTCACACA | 221178 |
rs551513045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197752 | CCTTATTTCCATGTT[C/G]TGACTAATTTTAAAA | 221178 |
rs551541773 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241331 | AAGAAGGGACAACTT[A/G]ATGACCCTGTCTGCC | 221178 |
rs551545360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980233 | CCCCAGCAGGCTCAA[G/T]GGGTGAGCGCATAGG | 221178 |
rs551549802 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167967 | CTCTCTCTGTCAGCA[C/T]GGACAAAGTAGGGTT | 221178 |
rs551553390 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24174514 | ATTCCACACATTTTT[A/T]TGTGTTGCATTTTCA | 221178 |
rs551563067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016515 | CCACAATGCTAGGCT[A/C]AAAGGTGCCCTTCTT | 221178 |
rs551565072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010563 | GGGCTTAGTGATTTC[G/T]GGGTCCCAAGATTTA | 221178 |
rs551576408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146029 | ACTTGGACTGAACAG[A/G]TAGCACAAGGTCCCT | 221178 |
rs551583338 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283539 | TGACTAGCAGGGTGG[A/C]CAATCTAAAAAGCTG | 221178 |
rs551590721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252398 | GTGACCTCATCTTAA[C/T]GTGATTATCTACCTA | 221178 |
rs551597145 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24046129 | ACATATGCAGAAAAG[C/T]GTCTAAGTCAAGTGT | 221178 |
rs551625856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221472 | TTGGCCTGATGGGAA[A/C]GGTTAAGGGGGAGCA | 221178 |
rs551626200 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24081064 | TATTCATTCATCTAA[A/G]CATTTATTTCCTGTC | 221178 |
rs551634254 | snp | A/G | | | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160029 | CACAAGAAAGGTGAT[A/G]GGCCTTTGAGTCGGT | 221178 |
rs551636057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24265530 | TAGAAAGTGCAGCCC[C/T]GTCTCAGCTGTGGGA | 221178 |
rs551658468 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305653 | CTCTCTCCCGCCTCT[A/G]TGCCTTTCTCTCTTT | 221178 |
rs551677954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028064 | AATTTTTAATTTCCA[A/G]ACATATAGCCATAAG | 221178 |
rs551683022 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084450 | GTGCGAGGTACACAG[A/G]ACACTTTTTGCACCC | 221178 |
rs551686637 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125673 | GATTCAAGGGATGGA[A/C/T]GTTTTTGTTGCTCAG | 221178 |
rs551688163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235019 | AATAATGCATGTATG[A/G]TACTTACCACAGTGC | 221178 |
rs551699962 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24133343 | TTGGAAATAGTGGCT[C/G]CTGGGACATTTGAGA | 221178 |
rs551713126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021936 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTAAT | 221178 |
rs551729041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:24269971 | AAGCAATCCTCCTGC[A/G]TCATCCTCCTGAGTA | 221178 |
rs551734642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228202 | CACTGCAAGCTCCAC[C/T]TCCCGGGTTCACGCC | 221178 |
rs551763883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276026 | AAATTGGAACTGTTG[C/T]GCACTGTTGGTGGGA | 221178 |
rs551768106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139484 | TCACTGGCAGGTGAC[A/T]GGTACAATTGCAGAG | 221178 |
rs551780491 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24300999 | GCGGTGATTCCCTAA[G/T]CTCCATGCACATTAG | 221178 |
rs551781322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080751 | ACTCATCTTCTGTGC[C/T]CTATGGCATGTGGAA | 221178 |
rs551788107 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24209543 | TCTGTGCCTGGCTCA[C/T]TTCACTCAGCATAAT | 221178 |
rs551797731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041005 | TGGGTCACATGGTTA[C/T]AGCTGCATGTGGACA | 221178 |
rs551803927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179584 | CAAAACTGAAACTCT[A/G]TACAGATTAAATGCA | 221178 |
rs551805425 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24026678 | CGCCTCCCGGGTTCA[C/T]GCCATTCTTCTGCCT | 221178 |
rs551815021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060257 | CCAGTGGAACAGAAT[A/G]GAGAGCCCAGAAATA | 221178 |
rs551815570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155852 | TCCCCACTTTCCCAC[C/T]GCAGCCTCTGGCAAT | 221178 |
rs551821182 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158924 | CCATTCATCTGAGGG[C/T]CAGGCCTGTTTCCCA | 221178 |
rs551831732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130907 | CAGGTTAAACTGCTG[A/G]AAAGAAAGCTCTGAT | 221178 |
rs551833768 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24181396 | GTTTTGTGATAACAC[C/T]TAGCTTAAAACACAA | 221178 |
rs551847504 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097982 | AAAACAGAAGGACCT[A/C]CATGAGGTTCAGACT | 221178 |
rs551856697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276769 | CCTTAGATAAGAAGT[C/T]ATCATTATTAACTTT | 221178 |
rs551879565 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24172842 | TAATGTTAGAATAGT[C/T]GTCTCTCCATCAACA | 221178 |
rs551879959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24158445 | CGTCCTAATCTCTGA[C/T]TTAACAGAATGGAAA | 221178 |
rs551891944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125181 | TTGCGTGGAGAGGCC[A/G]CTACACTGGCTCTGG | 221178 |
rs551892995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281481 | GGCTGTCGCGGTGTC[C/T]GGCGCACCTGTCTGG | 221178 |
rs551898580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054010 | TGTCGTTGGGGTGAC[A/G]GAGGCTCCTGGACAG | 221178 |
rs551901037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202634 | GATAAAAATGGAATT[A/G]AAAAGCCTGAAGGGA | 221178 |
rs551907703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982956 | CGTCTGGGAAGAAGG[C/T]GAGAGAAACTCTTTC | 221178 |
rs551917118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092018 | CACCGTTCTTCCTGA[C/T]GGTTAGTCATAGTCT | 221178 |
rs551920356 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085993 | AGACTGAAGCAAGTG[C/G]AGAGAGGATGAAGGA | 221178 |
rs551932379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24247259 | TGCTGGAACCTGCAC[A/G]GGATTGTCTTTTGAG | 221178 |
rs551940990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24174137 | AGATTCACTTTCCTT[A/G]ATGGTTAAGGGCTGT | 221178 |
rs551952285 | in-del | -/CACA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24054735 | GGTTTAATACTACCT[-/CACA]CACAGGAGAAAAGGT | 221178 |
rs551964285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201930 | TGCCTTTTCCAGAAT[G/T]TCATGTAGTTGGAAT | 221178 |
rs551971484 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288021 | CCAGTGTTTAGCTTC[G/T]TTGTGCCAGCCATCT | 221178 |
rs551972233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010623 | TGCCTGGAAGCTCCT[C/T]CACCTGTGGCCTGAG | 221178 |
rs551978422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092643 | AACTCTATACAAGAG[A/G]ATATTTTCTGCTGCC | 221178 |
rs551997359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094985 | TGATGTAGCCACTAT[G/T]TAAAACATGGAGATT | 221178 |
rs552008816 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002933 | TTAGAAGTGGCTCAA[A/T]GAAATATTTTTCTTT | 221178 |
rs552019463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294069 | TGGACATGCTCTGTG[A/C]TAGCCTGTGTGTAGA | 221178 |
rs552019752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280692 | ACAGTTCTTGGGCCT[C/T]GTGGTCTGGGCAGCC | 221178 |
rs552044817 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999754 | TTCTTATATTTAGGT[A/T]GCTTTTATTTTCAGT | 221178 |
rs552048201 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23988817 | TGTTCATTTGTCAGT[C/G]GGGCTGTTGGGTTTT | 221178 |
rs552058898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088643 | CCCAAAATGGAATAA[A/G]AAAATCAAAGCTCAG | 221178 |
rs552062312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24293595 | TTGTCTTAAGTAAAA[A/C]AAAGCAAAAATTCTT | 221178 |
rs552065550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173114 | ACACAGTCTTGCTCC[G/T]TCATCCAGGCTGGAG | 221178 |
rs552069094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047847 | ACAGGATCTGCTGTC[C/T]GTAACCTGGAGATGT | 221178 |
rs552091309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006882 | GAGGATGCCCCCGCT[C/T]GGCAATTAACACGAA | 221178 |
rs552092785 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24154242 | TTTTCCACTAAAAGC[A/G]TGTTCATGTCCTGGC | 221178 |
rs552097031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004862 | ACATTAAACCACAAA[A/C]CCTTCCCATTATCAA | 221178 |
rs552104355 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24119886 | ATGCTTTGGGACAAT[A/G]TCCTGATAGTAAACA | 221178 |
rs552107753 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285698 | TTTTTTTTTTTTTTT[G/T]GAGACAGAGTTTTGC | 221178 |
rs552114792 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189884 | ATATAATTATATATC[A/G]TAATATATATTATAT | 221178 |
rs552143984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24299230 | TAGTGGGGGCATCCT[A/G]TGTGCTTTCAACAGT | 221178 |
rs552162828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042580 | ATCTATGCCCGTGCG[C/T]GAACTCACTTCTCAG | 221178 |
rs552163452 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996781 | CAAGAGGCTGCCAGC[A/G]TTCCTTGGCTTGTGG | 221178 |
rs552164091 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133320 | TGGTAGAGATTGTGT[A/G]AGCCCAGTTGGAAAT | 221178 |
rs552169790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078102 | GCTCTCCTCCTGCAC[A/G]TGTGTCAGAGCTCTG | 221178 |
rs552179357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001714 | ATGTTCAATGATGGC[C/T]GTGGATATGGAGGGA | 221178 |
rs552189248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099982 | GAACCGTGACTGGCC[C/T]AGGGTCCACGGAGGG | 221178 |
rs552194926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025566 | CAAAGTAGTTGTTCC[A/G]ATTTATATGTAAAAC | 221178 |
rs552197001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094291 | GAACTCAGGGTTAAC[A/G]TAGAAAAACCAGGTT | 221178 |
rs552203845 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233769 | CTAGTTAAACCGGCA[A/G]ATTATGTACTTGTGA | 221178 |
rs552204468 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24203094 | GGTATTAAGCCCAGC[A/G]TCCATTAGCTATTCT | 221178 |
rs552204506 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24226386 | ATGATGCTTGTTTAA[A/G]GAGATTTTTATGATG | 221178 |
rs552209263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983480 | GAATTTTGAGCCCAG[A/G]GCAGAGAATTTTTAA | 221178 |
rs552218911 | snp | A/C | 0.00119737 | 0.0244387 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223305 | GTCCTGAAAGGAATT[A/C]AGAGCCGAGAGGGGT | 221178 |
rs552236728 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24113193 | ACCACTATATCTGCA[C/T]GTGCCAAAGGAAAAC | 221178 |
rs552244475 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018559 | AGATTATGTTTAGGT[A/C]TCAGAAAACCTGAGA | 221178 |
rs552251353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990307 | CAAAACCCTTTGATG[A/G]CCACCACTCCCCCAG | 221178 |
rs552279390 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24006743 | GGTGGAGCTGGGAGA[A/G]CACCGGGACACGCAG | 221178 |
rs552279477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112385 | CTCCCCACATTGTAT[A/G]ACAATCAATCCTACA | 221178 |
rs552280580 | snp | C/T | 0.000247368 | 0.0111186 | synonymous-codon | SPATA13 | GRCh38.p7 | 13:24286297 | ACTGGGCTTCAAAGC[C/T]GGGGATGTCATCCAG | 221178 |
rs552300850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199709 | GTTTGCCTAGACCTG[C/G]GGCAATGTATTGGAA | 221178 |
rs552310961 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123178 | GAGCCTGCATTACAG[G/T]TCTGATGAATGGTGT | 221178 |
rs552328569 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189214 | TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 221178 |
rs552337446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101957 | TGGGTGGGCGAATAT[C/T]TGCTCAAGACCTTGC | 221178 |
rs552347048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301911 | ATTTAATTCTCATAG[A/C]AACCCCATAGGTACT | 221178 |
rs552347472 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190223 | AACATATCATATATA[-/AT]ATATATATTATTATA | 221178 |
rs552349199 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106686 | GACAGAGCTGGCTCT[C/T]GTTCCAGGGCAAACT | 221178 |
rs552352020 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24125366 | TTGGGAAAAGAAACT[C/T]AGGACATTTCAAGCC | 221178 |
rs552354768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24128291 | GGACAGGAAAGGACA[A/T]TGTGGCTTCATCACC | 221178 |
rs552378513 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24231251 | AGAAAGAAGCCTCGC[A/G]CCATTTGCAGTCACT | 221178 |
rs552383308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24088991 | GGGTTTATGACAAAA[G/T]AAACCTGCACAAATG | 221178 |
rs552394584 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24148291 | CTCAGGGTTCAAGGG[A/G]TCTCAGTCCTACTTT | 221178 |
rs552400784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102536 | CTGGAGTGCAGTGGC[A/G]CAATCTTGGCACACT | 221178 |
rs552402962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096203 | AACAGACATAGCCCA[G/T]GTTCACGTGGAGCTT | 221178 |
rs552405454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122307 | TTTGAAACTATTCAA[A/C]CTATCGATTTGAATA | 221178 |
rs552421924 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291723 | CAAGCAACAAAATAC[A/C]CTCTCTCTCTGTCTT | 221178 |
rs552425981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24205627 | GCCTGAATAGTGAAG[A/G]CAATTCTAAGCAAAA | 221178 |
rs552426751 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984364 | TTTATATTCTGCCTT[C/G]AAAGGGAGGGAGAGT | 221178 |
rs552433230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24014558 | ATAATATTTGAAAAT[A/C]ATAAGAAAGAGAAAA | 221178 |
rs552439863 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24007414 | CAAAATCCTGCTGCA[C/G]CAGGGACAAGCTGGG | 221178 |
rs552442851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198245 | TGATCTGCCCCCCTT[A/G]GCCTCCCAAAGTGCT | 221178 |
rs552448309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204470 | GACGACTTTAACCAT[C/T]TTTAGGCATAAAATT | 221178 |
rs552463696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122546 | CTGGTCAGTGCCACG[C/T]CCTTTGCACTGCAGA | 221178 |
rs552465237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255449 | TCTGTTTTGTTCCTG[G/T]GGACCCCGAGATCAG | 221178 |
rs552467620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24116968 | GCTGGGAAGAGAGTA[C/T]TGACCAGGAACTTAA | 221178 |
rs552471407 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082123 | TTACTGCAATCTACT[C/G]TGTGCCAACCTCTAT | 221178 |
rs552491738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217707 | AGGAAGTTGCTACCA[C/G]CCCCTGGGCTGGAGT | 221178 |
rs552493417 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24093418 | CGTATGGTTAGTGAT[A/C]TAGGTTTTCCGAAGG | 221178 |
rs552513805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246779 | GAGACAGGATAATCA[C/T]TTGAACCTGGGAGGT | 221178 |
rs552518656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176925 | TGTGCCACCACGCGC[A/G]GCTTATTTTTGTATT | 221178 |
rs552519934 | snp | A/G | | | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255685 | TGTCACATGGGAGAT[A/G]CAGCCCAAGGGGTGG | 221178 |