SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6583 | snp | C/T | 0.460252 | 0.135255 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24307046 | ATGAATTTTAATATA[C/T]AAAACAACAAATATA | 221178 |
rs715921 | snp | C/T | 0.425894 | 0.177655 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221351 | AATAACCATAAAAGA[C/T]TACCAACTTTTAAGT | 221178 |
rs724932 | snp | A/T | 0.378372 | 0.214524 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995972 | CTATCTGCTCGGTTG[A/T]CTCTCTAGCTCTTCA | 221178 |
rs727113 | snp | C/T | 0.364401 | 0.222289 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112702 | GACTGAGAAAGTAGA[C/T]GAAGACTGAGACATC | 221178 |
rs728096 | snp | C/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220291 | TTCTTGGTTATAAAA[C/G]GTCTTATAGTGCCCT | 221178 |
rs728097 | snp | C/G/T | 0.552443 | 0.192851 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220247 | GCACCAAGGTTAGGC[C/G/T]GATTCCCATGTCTTG | 221178 |
rs736081 | snp | C/T | 0.499885 | 0.00758699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085587 | TCCAGAGGAAGGTGC[C/T]CCTTCTGCCACCACG | 221178 |
rs737529 | snp | A/G | 0.491263 | 0.0655142 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133973 | TGAGGAGGGGGCTGG[A/G]TCGAGCCCCTGGGGG | 221178 |
rs745918 | snp | A/G | 0.495483 | 0.0473088 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083274 | GTCCTCTTGCAGGCC[A/G]TGAGTGACACCAGCT | 221178 |
rs745919 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083330 | CACCAAACCCTGCCC[C/T]GCCCACAGGAGTCCA | 221178 |
rs746798 | snp | A/G | 0.459687 | 0.136129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040259 | CACTGAGTGCTCTCT[A/G]TGCATCCAGCTCTGG | 221178 |
rs747310 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134525 | CATTTCCCATTGGGA[C/T]GCTTTGCTAATCCAG | 221178 |
rs747311 | snp | A/T | 0.0584853 | 0.160693 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134486 | TAAGCTGCCAAAAAG[A/T]GATGTGCTGCTCTCG | 221178 |
rs754134 | snp | A/G | 0.499203 | 0.0199521 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990616 | TAGTGGATTCTTCTC[A/G]GATCCAGCATGTCCC | 221178 |
rs754135 | snp | A/G | 0.499053 | 0.0217445 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990651 | CTTGCAAATTGCCCT[A/G]TGCTATAATTGTCTA | 221178 |
rs756025 | snp | C/T | 0.325799 | 0.238232 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094381 | CCTACAATGTTGATC[C/T]GTTTTTCACAACCCT | 221178 |
rs756026 | snp | A/G | 0.481087 | 0.0953875 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094259 | CATTTGTGAGGCCAC[A/G]ATGTTCTCGCCAAAG | 221178 |
rs871970 | snp | C/T | 0.489492 | 0.0717183 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050398 | TTATAACAAGGATAT[C/T]TGATTTCTTGTGAGG | 221178 |
rs872196 | snp | C/T | 0.309154 | 0.242901 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992598 | TCATCATACATGGGA[C/T]TACCCCTGCCAACAT | 221178 |
rs873868 | snp | A/G | 0.306927 | 0.243432 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991320 | CTACATTCTGCAAAC[A/G]CAGGATTTATTGCCC | 221178 |
rs877039 | snp | C/T | 0.250732 | 0.249999 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078588 | GTCCCAGCATGGTGC[C/T]GACAGCAGCAGGCCT | 221178 |
rs880357 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255497 | tggtcatctgaatgg[C/T]ttgacctgtgaaatc | 221178 |
rs881428 | snp | C/T | 0.490782 | 0.0672626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236041 | gtgacagtccttgaa[C/T]ttttccaagcctcag | 221178 |
rs882554 | snp | A/G | 0.270621 | 0.249148 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011704 | ACTAGTTAAGCAGGA[A/G]CCTGGGAGTCTCCAA | 221178 |
rs883262 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024473 | TCTTCTTGCATGTGG[C/T]TGGTCTTGTCACTAG | 221178 |
rs883645 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058060 | GCAAGATGAGCTCCC[A/G]TCTGGCCATGCTGTG | 221178 |
rs883646 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058256 | TTGAAAACTCTCTAC[C/G]TGATATTGTTATCTG | 221178 |
rs912136 | snp | C/G | 0.5 | 0.00019968 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086828 | CATTGCTGGCTTCAG[C/G]TGCTGCCACTACCCA | 221178 |
rs912137 | snp | G/T | 0.5 | 0.00019968 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086827 | ATTGCTGGCTTCAGC[G/T]GCTGCCACTACCCAG | 221178 |
rs912138 | snp | C/G | 0.250168 | 0.25 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086557 | TCGCCAGTCCCCAAG[C/G]CTACAGACCCAGCCA | 221178 |
rs912139 | snp | A/G | 0.24449 | 0.249939 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085873 | TGCGCCCTGGTTCCG[A/G]TGCTTTGCACTATTA | 221178 |
rs912140 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24084745 | GATGTGAGCCACTGC[A/G]CTGCGCCACTTCATT | 221178 |
rs912141 | snp | C/T | 0.404209 | 0.196773 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253297 | ATTTCCAAAGAGTGT[C/T]ATTCTAATGACACTC | 221178 |
rs912142 | snp | A/G | 0.404559 | 0.196498 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253362 | TCTCTCTTCCCTAGA[A/G]GGAGACACCCAGATC | 221178 |
rs912143 | snp | C/T | 0.336245 | 0.234652 | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24253606 | AACAGATTCCATAAG[C/T]CAATATGTAGGATGC | 221178 |
rs912144 | snp | C/T | 0.405429 | 0.195811 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254522 | CTTCCTTCTCTGTGA[C/T]GTTCTGGGCCTGGAT | 221178 |
rs912145 | snp | A/G | 0.405603 | 0.195673 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254541 | CTGGGCCTGGATGGC[A/G]TGTGAGATGCTGCGA | 221178 |
rs912146 | snp | A/G | 0.345704 | 0.230956 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254689 | TGCAATCAGCTTTCC[A/G]CAAGGGGCTGTCTGG | 221178 |
rs912147 | snp | A/G | 0.210605 | 0.246877 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204210 | TACAGGAATAATACC[A/G]TTTAATTCTCACTGC | 221178 |
rs912148 | snp | C/T | 0.21303 | 0.247251 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204247 | CCAGAGTCTCTGTTA[C/T]TGTTATCCACATTTT | 221178 |
rs912149 | snp | A/G | 0.213333 | 0.247296 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204307 | CACTGTGTTCAGAAA[A/G]CGATAGGAAAATTGT | 221178 |
rs912150 | snp | A/G | 0.442791 | 0.15916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078747 | GCATGGAATGGGAAG[A/G]TGAATGTACACTGAT | 221178 |
rs912151 | snp | A/G | 0.397452 | 0.201886 | intron-variant | SPATA13 | GRCh38.p7 | 13:24078410 | CATATACTTCAGACT[A/G]TTACTGTGAGTCTTC | 221178 |
rs912863 | snp | A/G | 0.153332 | 0.230554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099548 | TGTGCTTCAGACCCC[A/G]TGCATCCACAAGCAC | 221178 |
rs912864 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | SPATA13 | GRCh38.p7 | 13:24083434 | GGGCAGGCCTGACCT[C/T]GGCCACAGGTGCTGC | 221178 |
rs912865 | snp | C/T | 0.498084 | 0.0308911 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041910 | TACATTCCAATTGAC[C/T]GTTACGCCTCACTCT | 221178 |
rs912866 | snp | A/G | 0.498084 | 0.0308911 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041904 | CCAATTGACCGTTAC[A/G]CCTCACTCTGATTCC | 221178 |
rs912867 | snp | C/T | 0.498109 | 0.0306926 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041803 | CCCTTACCTGTCTCA[C/T]GCTTTCCCACCTTCC | 221178 |
rs912868 | snp | A/T | 0.5 | 0.000399361 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990463 | GTGCTGAAACAAGGG[A/T]GCACCCTGAGTTTAA | 221178 |
rs912869 | snp | C/G | 0.498253 | 0.0295011 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990216 | GATCATAAAACTGCT[C/G]AATGTGGAAAAGTCT | 221178 |
rs912870 | snp | C/T | 0.242488 | 0.249887 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011946 | TGTGCACCTCCGCCT[C/T]CCCCTACGGATTGTA | 221178 |
rs912871 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012660 | CCGTCTTCCGCAGCC[A/G]ACCCCCAAGTGTGTG | 221178 |
rs927552 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234367 | TTCCATATTCTTCAG[A/G]GGGGGAATTTTAGCT | 221178 |
rs927553 | snp | C/G | 0.49089 | 0.0668743 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234566 | AGAAGGAATGCCGTA[C/G]GTTTTGTTGGTGGGG | 221178 |
rs927764 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989816 | gcaccaaccctgttc[A/G]tcaggcttctgtcct | 221178 |
rs942109 | snp | C/T | 0.225597 | 0.248806 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065868 | GCTCTGAAGTCCAAA[C/T]ACTTGGGTTTGAATC | 221178 |
rs942110 | snp | C/T | 0.225301 | 0.248777 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065904 | TCTGCCACTTAACAA[C/T]TTGACTTGTCTTGGA | 221178 |
rs942872 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058384 | CCGTAATCCCTTCAG[C/T]AGGGAATTCTGATAT | 221178 |
rs942875 | snp | A/G | 0.382279 | 0.212137 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040611 | GGGGTCCAGGACACA[A/G]AGCCTGCCAAGCACC | 221178 |
rs942876 | snp | A/G | 0.448066 | 0.152544 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040812 | TGATTGTTTGCTGTC[A/G]TTCCTTTATAAAACT | 221178 |
rs942877 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990952 | GCCAACTCAGCTTTC[A/T]CTTCTTGCCACACAG | 221178 |
rs942878 | snp | C/G | 0.479984 | 0.0980171 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990742 | GGTTCTGGGTGATCA[C/G]GGGAAACAAGGTAGA | 221178 |
rs942879 | snp | C/G | 0.491157 | 0.065903 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990728 | ACGGGAAACAAGGTA[C/G]ATGTGATCCTGCTCC | 221178 |
rs942880 | snp | A/G | 0.348574 | 0.229746 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986221 | TGGAATTTGGCATAT[A/G]GTTTCCTTAGAAAGA | 221178 |
rs942882 | snp | A/C | 0.482234 | 0.0925596 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100130 | TTTAAACTATTTAAA[A/C]ATTATAAAATAAATC | 221178 |
rs947227 | snp | A/G | 0.496616 | 0.0409947 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301932 | AATCCCTAAAACGGG[A/G]ATTACAGTACCTATG | 221178 |
rs947228 | snp | C/T | 0.49681 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301891 | GAGAATTAAATGAAT[C/T]AATAGAAGTAAAGTG | 221178 |
rs947229 | snp | C/T | 0.496649 | 0.0407971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301652 | AGAAGGCTCTCCCTA[C/T]CTCCCGAGGTGGCAG | 221178 |
rs947230 | snp | G/T | 0.496842 | 0.0396107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24300788 | GGATGTGCGTGACCT[G/T]GTGGCTAACACCATC | 221178 |
rs956382 | snp | C/T | 0.409212 | 0.192748 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112821 | AAGAATCTGAAGCAA[C/T]GACAGCAAAGACCAA | 221178 |
rs958993 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996212 | GGCCTCAGAAGGAAA[A/G]CAATCCTTGAGTCAG | 221178 |
rs976418 | snp | G/T | 0.163564 | 0.234582 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073847 | CTCAGTTCACAGCCT[G/T]CCTGAATATTCATGG | 221178 |
rs989513 | snp | C/T | 0.465158 | 0.127307 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143453 | CGCAGCTGCTGGCAG[C/T]GCTCTCATTCCTATG | 221178 |
rs989514 | snp | C/T | 0.465473 | 0.126772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143502 | AAATTGATAGTTACT[C/T]CTATTTTTGCAAAGA | 221178 |
rs1001784 | snp | A/C | 0.272241 | 0.249009 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980081 | CGCACCTATAGCTCT[A/C]TCCCTTCTCCTACCC | 221178 |
rs1012035 | snp | A/G | 0.488666 | 0.0744214 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056430 | GTCTTGTATGGAAAT[A/G]GAATAACAAGCCTAA | 221178 |
rs1022825 | snp | A/C | 0.465263 | 0.127129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097163 | AGCTGTCAGTGCACC[A/C]GGCATGGGTGGCTGG | 221178 |
rs1022826 | snp | C/G | 0.434687 | 0.168495 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097312 | CTTACAAATGAGAAG[C/G]TAAATAATTTCCCCA | 221178 |
rs1028695 | snp | C/T | 0.385932 | 0.209815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178628 | ACTTAGTGAACCAAG[C/T]AGACCCAGTCTATCT | 221178 |
rs1028696 | snp | A/G | 0.386313 | 0.209568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178795 | agatctaattgatat[A/G]taacgcatccattta | 221178 |
rs1028697 | snp | C/T | 0.474091 | 0.11083 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178844 | tttttagtgtatcca[C/T]ggagtcatgcactca | 221178 |
rs1028698 | snp | C/T | 0.364401 | 0.222289 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061807 | aaataatctttacaa[C/T]aaactcctgagttta | 221178 |
rs1028699 | snp | A/T | 0.358303 | 0.225323 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061872 | aacataaaagttttt[A/T]aaaaaaattaaaaat | 221178 |
rs1028700 | snp | A/G | 0.252983 | 0.249982 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062439 | TCTCCAATGGCGCCA[A/G]GGTGCACGGTGCTGG | 221178 |
rs1028701 | snp | C/T | 0.239902 | 0.249796 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062671 | ACCCAGTGAAGTATC[C/T]TCATGACTGCACCTG | 221178 |
rs1033848 | snp | A/C | 0.463234 | 0.130503 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140540 | AGAGCTGTTTGGATC[A/C]AAATTCAGCCTCTCC | 221178 |
rs1033849 | snp | A/G | 0.453939 | 0.144598 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140628 | GCGTGTCCTTCTGAG[A/G]CAGCTCTCAAGCTTT | 221178 |
rs1033850 | snp | C/T | 0.469839 | 0.119042 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140706 | GCAGCGTATTTAAGT[C/T]AAAGAGCCAAGAATG | 221178 |
rs1033851 | snp | A/T | 0.47023 | 0.118317 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140729 | CAAGAATGTTAGTAT[A/T]ATATAATGAAGTGAA | 221178 |
rs1033852 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250615 | TAAAAGGGAACTCCT[A/G]TGGAGTACTAGTACT | 221178 |
rs1041131 | snp | C/T | 0.307423 | 0.243316 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981879 | AAAAGAAAATTGCAT[C/T]ACAGTTATTGTTTTT | 221178 |
rs1113414 | snp | A/G | 0.414576 | 0.188188 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053589 | CTGGGCCCACGGTGG[A/G]AGTATTTTTCTCTAT | 221178 |
rs1117357 | snp | C/T | 0.498568 | 0.0267188 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047042 | aatcagcagcactca[C/T]tccctagcctgctgt | 221178 |
rs1124510 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24288370 | TCATGACATTCAGTA[C/G]AATAAACTGACCATG | 221178 |
rs1125959 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061790 | TTCATACCTGGGTGA[C/T]GAAATAATCTTTACA | 221178 |
rs1129021 | snp | A/G | 0.417521 | 0.185571 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305565 | CCTGATTTGAGTCAC[A/G]TGTTCCACTTGGAAA | 221178 |
rs1138013 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24302297 | AGAATTAGCTCTCTA[A/C/G]AAAAAAATATAAAAA | 221178 |
rs1220545 | snp | C/G | 0.00329302 | 0.0404434 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24223195 | GTGCCCACCCCGAGC[C/G]GCCCCACTCCATGGT | 221178 |
rs1220546 | snp | C/T | 0.412198 | 0.190241 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223775 | CAGGACGGCCCATGA[C/T]GCACGGGTACCACAG | 221178 |
rs1220547 | snp | C/T | 0.497614 | 0.0344582 | synonymous-codon, intron-variant | SPATA13 | GRCh38.p7 | 13:24223982 | GGCCAGCCTGAGACT[C/T]CAGGCACACAGCCGG | 221178 |
rs1220548 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225375 | cttccgctgcaggca[C/T]cagcgtgtggacgag | 221178 |
rs1220549 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24227361 | TAGTTATTTGCCAGG[A/G]TGATTTTGACCATTT | 221178 |
rs1220550 | snp | A/G | 0.499994 | 0.00179711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228083 | ctaattttttgtaaa[A/G]atagggtttctccCC | 221178 |
rs1220551 | snp | A/C | 0.499971 | 0.00379382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228611 | ACAGGAAAAGGGTGA[A/C]ACGCAAGGATTCCAG | 221178 |
rs1220552 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | SPATA13 | GRCh38.p7 | 13:24228748 | GTAAGGTTCTACTTA[C/T]AGGATTAAAGCAAAT | 221178 |
rs1220553 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SPATA13 | GRCh38.p7 | 13:24229171 | ATTCATGCTGCTTCT[C/G]CTACCAGCTCACAAG | 221178 |
rs1220554 | snp | C/T | 0.480853 | 0.0959518 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191595 | gctcactgcaagctc[C/T]gccacccgggttcac | 221178 |
rs1220555 | snp | C/T | 0.480853 | 0.0959518 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191602 | gcaagctccgccacc[C/T]gggttcacgccattc | 221178 |
rs1220556 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192914 | GAGCACTGGTAGAGA[C/T]GGACAGGAGGAAAAG | 221178 |
rs1220557 | snp | C/T | 0.154329 | 0.23097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193948 | AGAAGGGTGGAAGCT[C/T]TGAGGACTATAGAGA | 221178 |
rs1220558 | snp | A/G | 0.181659 | 0.240478 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193965 | GAGGACTATAGAGAC[A/G]CAAAAAGGCAGAAAC | 221178 |
rs1220559 | snp | A/G | 0.139225 | 0.224118 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194305 | ATGACTTACAAAAGA[A/G]GAAAAGAAAAGTTAG | 221178 |
rs1220560 | snp | A/G | 0.227074 | 0.248947 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194507 | TAGCTGGAGAGGTAG[A/G]ATGCATGCTCTGAGT | 221178 |
rs1220561 | snp | C/T | 0.153 | 0.230415 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194930 | TTCATGGGAAGTGGA[C/T]GATACAACTTTTTAa | 221178 |
rs1220562 | snp | A/G | 0.154993 | 0.231244 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195044 | tgtacagctgttgcc[A/G]ctgattccaggacct | 221178 |
rs1220563 | snp | A/T | 0.498693 | 0.0255257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195979 | ATTAAAAATTTAAGC[A/T]TGTTTCATATTATCT | 221178 |
rs1220564 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196062 | CATTTGATTTTAATT[C/T]TTTGGTGCCAAGAAA | 221178 |
rs1220565 | snp | C/T | 0.491473 | 0.0647364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196114 | TAACTTACTGCAGAG[C/T]TTTCAAAATATCTTA | 221178 |
rs1220566 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197223 | AATATTTATGTGATG[A/G]AATAGTCAAGTATAA | 221178 |
rs1220567 | snp | G/T | 0.487368 | 0.0784625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197735 | ACATGTGCCATCCTT[G/T]GCCTTATTTCCATGT | 221178 |
rs1220568 | snp | A/G | 0.490453 | 0.0684267 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197747 | CTTGGCCTTATTTCC[A/G]TGTTCTGACTAATTT | 221178 |
rs1220569 | snp | A/G | 0.262435 | 0.249691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197894 | GCTGATTTTTCTCCT[A/G]GGATGAAGTCCCCCA | 221178 |
rs1220570 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163456 | CCAGCTGTCTCCTCC[C/T]GTGCATTGAGAGTTC | 221178 |
rs1220571 | snp | C/G | 0.191461 | 0.24305 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181139 | ttatgaatggagttt[C/G]caggactggaagttg | 221178 |
rs1220572 | snp | A/C | 0.188631 | 0.242351 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181628 | atcactgtctaccac[A/C]tccatccacatcttg | 221178 |
rs1220573 | snp | C/T | 0.159292 | 0.232964 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183024 | CTGAGGATATCTGCT[C/T]ACATATATTCCTCAT | 221178 |
rs1220574 | snp | C/T | 0.188 | 0.24219 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183305 | AGGATAGACATCATC[C/T]TTTATCACTTCCCTC | 221178 |
rs1220575 | snp | C/G | 0.16618 | 0.23553 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183665 | tattttatgcgtggc[C/G]caagacaattcttct | 221178 |
rs1220576 | snp | A/G/T | 0.658676 | 0.0533228 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183785 | ACTCCTGGGGTGAGA[A/G/T]GGGGGCGGGGTGAGC | 221178 |
rs1220577 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154906 | cttgttgcccaggct[A/G]gagtgcaatagcatg | 221178 |
rs1220578 | snp | A/G | 0.139903 | 0.224452 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156008 | gttgcagcgtgtgtc[A/G]gaattttgttcctct | 221178 |
rs1220579 | snp | A/G | 0.463343 | 0.130326 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156680 | TATCCATTCTAATCA[A/G]TGATAGCCACCAGTT | 221178 |
rs1220580 | snp | A/C | 0.040671 | 0.13668 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157083 | TCTGCTTCCCTAACC[A/C]GGTCTAGACCTTAAG | 221178 |
rs1220581 | snp | A/T | 0.499998 | 0.000998401 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159141 | GTGATATTTTTTTTT[A/T]AATAATACTAACATA | 221178 |
rs1220582 | snp | G/T | 0.233818 | 0.249476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167729 | CCTTCTGTGGCAAGT[G/T]ATCTGTCTTCTAGGG | 221178 |
rs1220583 | snp | G/T | 0.386313 | 0.209568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168030 | CTATTTCTGCCTCTT[G/T]ATGACGTAATTATTC | 221178 |
rs1220584 | snp | C/G | 0.426354 | 0.177198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24169376 | GGGATTCTGGGTAAG[C/G]AAAAGTGGCAGCTTC | 221178 |
rs1220585 | snp | A/G | 0.108048 | 0.20579 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260386 | TGTAAGGAGCTGGCA[A/G]ATCCCACAGTGTGGC | 221178 |
rs1220586 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260401 | AATCCCACAGTGTGG[A/C]CTGCGCTTGCCTTCC | 221178 |
rs1220587 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260429 | TCCTGGCTCCTCTTC[A/G]CTGGTCCCACAAGTA | 221178 |
rs1220588 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24260474 | CCGGGAGTCAAGAGC[A/T]TGACCCCACCAAGCC | 221178 |
rs1220589 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237311 | gaggttgcagtgagc[C/T]gagattgcaccactg | 221178 |
rs1220590 | snp | A/C | 0.081446 | 0.184634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237382 | caaaacaaaacaaaa[A/C]aaacatgctgcagca | 221178 |
rs1220591 | snp | A/G | 0.167919 | 0.236458 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238659 | AGGTAGGGGACAGGC[A/G]GCTGAAGTCTTGCAT | 221178 |
rs1220592 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240059 | CCTGTAATCTCAGCA[C/T]TTTGGGAGTCTGAAG | 221178 |
rs1220593 | snp | A/G | 0.359575 | 0.224707 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241602 | AGTGATGCCTGGACA[A/G]GTGGAAAGAGCCAGG | 221178 |
rs1220594 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241830 | TCCTGGGCTCAGGCA[A/G]TCCTCCCGCCTCGGC | 221178 |
rs1220595 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:24242154 | GTCTATGGAACCAAG[A/T]GTCGATTTTGTTTCA | 221178 |
rs1220596 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243139 | TTTCACATTATACAA[C/T]GGGTTTTTCTGATGT | 221178 |
rs1220597 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243875 | AAACTTTTGGTATGC[C/T]CAGAGTCCCTATGCT | 221178 |
rs1220598 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232617 | tgcaatcacagctta[C/G]tgcagcctcaacctc | 221178 |
rs1220599 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233622 | ATCATTTTCTAAGTC[A/G]GTTTAAAAAAAAAAG | 221178 |
rs1220600 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | SPATA13 | GRCh38.p7 | 13:24234079 | AAGGGGGGAGGTAGA[C/T]GGAATCATACCCCTA | 221178 |
rs1220601 | snp | G/T | 0.250168 | 0.25 | intron-variant | SPATA13 | GRCh38.p7 | 13:24236210 | TTAATCTTTCTTATC[G/T]GTAAAGTAGAATTAA | 221178 |
rs1220602 | snp | C/T | 0.483923 | 0.0882034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215005 | GTCCCTGGGATATTA[C/T]ACCAGAGTATTCCTG | 221178 |
rs1220603 | snp | A/G | 0.490287 | 0.0690083 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215423 | GGGCCTCTGTCCTCA[A/G]CAGTGGCAAAATGGT | 221178 |
rs1220604 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215568 | CACATTTTATGCAAA[A/G]ACAAAAAAATTGAAC | 221178 |
rs1220605 | snp | A/G | 0.447162 | 0.153712 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215671 | AATTAAGCTGTGGAT[A/G]TAAAAGCTACATCAT | 221178 |
rs1228438 | snp | A/G | 0.212425 | 0.24716 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181884 | ctttgggaggccaag[A/G]cgggtggatcacctg | 221178 |
rs1231459 | snp | C/T | 0.492087 | 0.0623997 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191551 | gtcttgctctgtcac[C/T]caggctggagtgcag | 221178 |
rs1236195 | snp | C/T | 0.213937 | 0.247385 | intron-variant | SPATA13 | GRCh38.p7 | 13:24181842 | agtataggccgggtg[C/T]ggtggcttaacacct | 221178 |
rs1237543 | snp | C/T | 0.328148 | 0.237472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165225 | GTCTTTGTGGAATCA[C/T]GAGAGCGCAGACATT | 221178 |
rs1238928 | snp | A/C | 0.00240384 | 0.0345853 | intron-variant | SPATA13 | GRCh38.p7 | 13:24217081 | aaacaaaaacaaaaa[A/C]AAAAAAAAGGAAATG | 221178 |
rs1318365 | snp | C/T | 0.120326 | 0.21374 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204454 | ataacgtaacattga[C/T]gacgactttaaccat | 221178 |
rs1325661 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24071118 | GACCAGAGGAACTAG[A/G]GATGCGTAGAAAACT | 221178 |
rs1325662 | snp | A/C | 0.402454 | 0.198136 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120391 | AGACAGCTTAGCCAT[A/C]CATCTTCCCCAAAGA | 221178 |
rs1325663 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120355 | AACACAGCCAAAGTG[C/T]CAAAGTTAGTGACCC | 221178 |
rs1325664 | snp | C/T | 0.361474 | 0.223771 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120348 | CCAAAGTGTCAAAGT[C/T]AGTGACCCAGGCGAC | 221178 |
rs1325665 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117507 | TGAATCAAAAACTGA[C/T]ATCACTAAAGTCATA | 221178 |
rs1325666 | snp | C/T | 0.368119 | 0.220336 | intron-variant | SPATA13 | GRCh38.p7 | 13:24117266 | ACAGACACTATGTCT[C/T]TATTAGATACACTAT | 221178 |
rs1325674 | snp | C/T | 0.140581 | 0.224783 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017116 | GGCCAGGGCAGAGAG[C/T]TGAGGTAACATCAGT | 221178 |
rs1409020 | snp | A/G | 0.225301 | 0.248777 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065818 | TGTCATTCTCAACTA[A/G]GTTTTTAAAAATATT | 221178 |
rs1409021 | snp | A/G | 0.225301 | 0.248777 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066014 | TAAATGAGATAGCAC[A/G]CCTGAAGCATTTGCC | 221178 |
rs1409022 | snp | C/T | 0.499325 | 0.0183582 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115990 | acttctgagactaga[C/T]cataaggttctgtgg | 221178 |
rs1409023 | snp | G/T | 0.49998 | 0.00319482 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115981 | actagatcataaggt[G/T]ctgtggctctcacct | 221178 |
rs1409024 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080908 | ACTTCCAGTGCACCT[C/G]TCTTCTGTCCCCTCA | 221178 |
rs1409025 | snp | A/T | 0.319616 | 0.240112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052080 | TTGGCTTCTTACACC[A/T]GCATCCTGTGCTGTG | 221178 |
rs1409026 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052099 | TCCTGTGCTGTGTCC[A/G]GGCTCCTCGGGTCTC | 221178 |
rs1409028 | snp | A/G | 0.472335 | 0.114312 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986868 | CCCATGATGTTTCCA[A/G]TCTGAGGAAACTGCA | 221178 |
rs1409030 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112384 | GTAGGATTGATTGTC[A/G]TACAATGTGGGGAGC | 221178 |
rs1409031 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112174 | GCTTTGCAAGAAGGA[A/G]TGGGGGGCAGAAGTG | 221178 |
rs1409032 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111994 | AACAAGAGTCTTTAT[C/T]CAATTCAAAACGATC | 221178 |
rs1475199 | snp | C/T | 0.377582 | 0.214995 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209536 | ttgtctctctgtgcc[C/T]ggctcatttcactca | 221178 |
rs1536199 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049458 | ggtttgtgtgagtac[A/G]ctccgtgttgttcac | 221178 |
rs1536204 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061573 | gtcttttatagggac[A/G]tggatggagctggaa | 221178 |
rs1536205 | snp | A/G | 0.45645 | 0.140991 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061762 | cagaaaaaaatcatg[A/G]atactaccaggcttc | 221178 |
rs1570460 | snp | A/C | 0.466515 | 0.124985 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197298 | GAAGAAATTGTAAAG[A/C]TGGAAAGAGTAAACA | 221178 |
rs1570461 | snp | G/T | 0.466618 | 0.124806 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197407 | GTATCATGAATATGT[G/T]TCAGAAATTTATTTA | 221178 |
rs1570462 | snp | A/T | 0.279461 | 0.248258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077501 | GATAGGAAATTTTTC[A/T]TCCCTCACCCACTCC | 221178 |
rs1570886 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055648 | CAAGGGTTCCAATAC[C/T]AGCTCTCAGGTGCTG | 221178 |
rs1570887 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056419 | TAAACTTACCTTTAG[A/G]CTTGTTATTCCATTT | 221178 |
rs1570889 | snp | C/T | 0.133093 | 0.220981 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050330 | CTAGTTCCTTGAAAT[C/T]TGATAATGCTGACGA | 221178 |
rs1570890 | snp | C/T | 0.137527 | 0.223271 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033643 | GGACCTGGTGTGGCA[C/T]TGAGTGGCTGTGAGT | 221178 |
rs1570891 | snp | C/T | 0.484771 | 0.0859212 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033731 | TGCTGATGGAGCAGT[C/T]GCCTCCACCTGGCTG | 221178 |
rs1808040 | snp | C/T | 0.474903 | 0.109173 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141003 | AACAAGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 221178 |
rs1810681 | snp | A/G | 0.157972 | 0.232445 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109353 | atgcccatcaatgat[A/G]gaccggattaagaaa | 221178 |
rs1810682 | snp | A/G | 0.157972 | 0.232445 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109351 | gcccatcaatgatag[A/G]ccggattaagaaaat | 221178 |
rs1830926 | snp | A/G | 0.499295 | 0.0187567 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121370 | ATGTAATGGGGTGTG[A/G]GGCAAGGGTAATTTC | 221178 |
rs1830927 | snp | C/T | 0.49934 | 0.0181589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121336 | TTATTAATTGAAAAA[C/T]GAACTAGCAATTTTG | 221178 |
rs1885901 | snp | A/C | 0.499295 | 0.0187567 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123933 | ATTTCCTCTTTCAGG[A/C]TTTTGAGATAACCTG | 221178 |
rs1886801 | snp | A/T | 0.412249 | 0.190198 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985760 | TATGTTGCCTGTGTA[A/T]CCTTCTGTCCTGGAA | 221178 |
rs1886802 | snp | C/T | 0.460027 | 0.135605 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027980 | AAATTGTTTTTGTTA[C/T]AATTCTGTTTTAGTA | 221178 |
rs1886803 | snp | C/T | 0.41275 | 0.189769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028026 | TATATTTTTCTTTGA[C/T]TCATAAATTTAGATG | 221178 |
rs1886804 | snp | G/T | 0.41275 | 0.189769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028035 | CTTTGATTCATAAAT[G/T]TAGATGTTTTTATAA | 221178 |
rs1886805 | snp | A/G | 0.41275 | 0.189769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24028355 | TCAGTTCATGTGCAG[A/G]TGTCTATATTTTGCC | 221178 |
rs1891103 | snp | A/T | 0.188316 | 0.242271 | | | GRCh38.p7 | 13:24305739 | AGAATGGAATAGGTG[A/T]AATTCATCAAAATGT | 221178 |
rs1891104 | snp | C/T | 0.0383715 | 0.133092 | | | GRCh38.p7 | 13:24199109 | ttgagctcaggagtt[C/T]gagaccagcctgagc | 221178 |
rs1891105 | snp | C/T | 0.48491 | 0.0855403 | | | GRCh38.p7 | 13:24274257 | TTCAGGTTAAGCTTA[C/T]TTAAACCACACCACA | 221178 |
rs1923898 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136332 | aaatacaaaattagc[C/T]gggtgtggtggcgca | 221178 |
rs1923899 | snp | A/G | 0.497121 | 0.0378299 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136439 | tgagatcgtgccatt[A/G]cactccagcctgggt | 221178 |
rs1923900 | snp | A/T | 0.49703 | 0.0384237 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136504 | aagaaagaaagaaag[A/T]gagagagagggagag | 221178 |
rs1923901 | snp | A/G | 0.49703 | 0.0384237 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136505 | agaaagaaagaaaGT[A/G]agagagagggagaga | 221178 |
rs1923902 | snp | C/G | 0.475259 | 0.108435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141235 | CCTGTAATTCCAACA[C/G]TTTAGGAGGTCAAGG | 221178 |
rs1923903 | snp | A/C | 0.475259 | 0.108435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141248 | CAGTTTAGGAGGTCA[A/C]GGTGGGAGGATCACT | 221178 |
rs1923904 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145243 | TCTGATTTTTTACAA[C/T]AGCCACAAAATACTA | 221178 |
rs1923905 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145435 | GAAGCTGTCTGTAGC[A/G]TCCCTACCAGCACGT | 221178 |
rs1923906 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145944 | GGGGGGAGCACTCCC[A/G]ACCAAGTCAACAGGC | 221178 |
rs1923907 | snp | C/T | 0.421368 | 0.182025 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200873 | AAATACACAGTTTCA[C/T]GTAATAGTCAAAATA | 221178 |
rs1923908 | snp | G/T | 0.484701 | 0.0861117 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200934 | TGACAGAATGTGTCT[G/T]ATTACGTCCTTGTTC | 221178 |
rs1923909 | snp | C/T | 0.398354 | 0.201224 | intron-variant | SPATA13 | GRCh38.p7 | 13:24124980 | ACTGAAACTCATTCA[C/T]AGGGTCAGAGCGGGT | 221178 |
rs1923910 | snp | A/T | 0.308661 | 0.24302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125140 | CTCTGTGAGGCTCTT[A/T]GTTTCTGCTCCCGCA | 221178 |
rs1923911 | snp | C/T | 0.377977 | 0.21476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24125975 | CAGCTGCCTTTGGCT[C/T]TGCTCCTGGCTTGGG | 221178 |
rs1923912 | snp | C/G | 0.36955 | 0.219562 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126013 | GTTCTTGGGGAGGTA[C/G]GAATAGAGCAGGGGA | 221178 |
rs1935042 | snp | C/T | 0.136166 | 0.22258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275992 | cacattctcaccaac[C/T]gtagtttcttttgtt | 221178 |
rs1935043 | snp | A/C | 0.110519 | 0.207473 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275852 | ttgcctccagggttc[A/C]agagattctcctgcc | 221178 |
rs1952099 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048541 | ACATCCTACAAATAT[A/G]GAATATATAACTTTC | 221178 |
rs1952100 | snp | C/T | 0.497668 | 0.0340657 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048840 | TTGTAGCAAATTTAT[C/T]GCATCCAGGAAAAGT | 221178 |
rs1969883 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050070 | tagagatagggtttc[A/G]ctgtgtggccaggct | 221178 |
rs1977255 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | SPATA13 | GRCh38.p7 | 13:24077701 | CAGCATAGTGTGTGC[C/T]GCTCTATAATACACT | 221178 |
rs1980696 | snp | A/G | 0.282632 | 0.247861 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085073 | CTCCAGATCAACATC[A/G]CCACGAAGGCACCGC | 221178 |
rs1983870 | snp | A/G | 0.36315 | 0.222928 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096024 | ACCAGGCTTAGCTGG[A/G]AAGTGACCCAGGCAG | 221178 |
rs1998477 | snp | A/G | 0.461259 | 0.133677 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147492 | TTCTCCGTTGGAAGT[A/G]GTGATTGCTCGGTGC | 221178 |
rs1998478 | snp | C/T | 0.481856 | 0.0935034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147635 | ATATACAGAACAAAA[C/T]GTACCATCTTAACCA | 221178 |
rs1998783 | snp | C/T | 0.370772 | 0.218893 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107596 | ATAAATATAAGAGTG[C/T]TAAGAGTTGGCATGG | 221178 |
rs2004641 | snp | C/T | 0.256994 | 0.251562 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222037 | TCACCTGAGGTCAGA[C/T]GTTCGAGACCAGCCT | 221178 |
rs2025304 | snp | G/T | 0.391024 | 0.206427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24062773 | TGTCCACATGCATTT[G/T]TTATCTTCCATCCTT | 221178 |
rs2027436 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220849 | GGGGCAAATAAAAAT[A/G]GAACCCATCAAGAAC | 221178 |
rs2027437 | snp | A/C | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221027 | CTTGGAGGTAATGGC[A/C]TTGACTGATGTCTAA | 221178 |
rs2027438 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221035 | TAATGGCATTGACTG[A/G]TGTCTAAAGATTTTT | 221178 |
rs2031156 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139883 | ccatcctgcctaaca[C/T]ggtgaaaccctgtct | 221178 |
rs2031157 | snp | G/T | 0.101658 | 0.201233 | intron-variant | SPATA13 | GRCh38.p7 | 13:24140036 | gtcgtgccactgcac[G/T]ccagcctgggtgaca | 221178 |
rs2031158 | snp | G/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219916 | ATTTGCAAGGAACTT[G/T]GCTGGTTTCAACCCT | 221178 |
rs2031159 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219957 | TATCCTGAGATACCC[C/T]TCATTCCTGGGTCAG | 221178 |
rs2031160 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220081 | GCGATTACCTTATCA[C/T]TGCCTTGAATTCCTC | 221178 |
rs2031161 | snp | A/G | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24220191 | GTAGACAGCACTGAA[A/G]TACAGATCACTGAAA | 221178 |
rs2031162 | snp | C/T | 0.485118 | 0.0849685 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159281 | AAGGTTTGGTTTTTA[C/T]ATTTTTTCAGCTTTA | 221178 |
rs2039924 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24284837 | CCCCTCCACTATCTC[A/G]TGTAATTCTCACAAC | 221178 |
rs2068032 | snp | A/G | 0.379354 | 0.213933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219481 | TAAGAAGTTGTTACA[A/G]CCCACTATGTTTTTA | 221178 |
rs2068033 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219404 | AGGATTCAGATTTCA[C/T]AAAACACATGCAAAA | 221178 |
rs2068034 | snp | C/T | 0.102726 | 0.202016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219351 | AATATGCTTTTTAAA[C/T]GACCAGTGACTTAGT | 221178 |
rs2077187 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204443 | gtaaaataggtataa[A/C]gtaacattgacgacg | 221178 |
rs2077899 | snp | A/C | 0.499325 | 0.0183582 | intron-variant | SPATA13 | GRCh38.p7 | 13:24123202 | ATGGTGTGATATATT[A/C]TTTAGCTTTTTCTTG | 221178 |
rs2093643 | snp | A/C | 0.494057 | 0.0541878 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204909 | aatgctgctgtgaac[A/C]tcagtgtataaatat | 221178 |
rs2094112 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978557 | acagcacatacgttc[C/T]tgtttttattaatat | 221178 |
rs2094113 | snp | A/G | 0.496034 | 0.0443518 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040455 | GAAATTCACAGCACC[A/G]CCCTTGACAGGAAAC | 221178 |
rs2094114 | snp | C/G | 0.494896 | 0.0502606 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040456 | AAATTCACAGCACCG[C/G]CCTTGACAGGAAACC | 221178 |
rs2096083 | snp | C/T | 0.485596 | 0.0836329 | intron-variant | SPATA13 | GRCh38.p7 | 13:24274198 | TTTGTTGCCTGTCCA[C/T]GCAGCAAGCCACAAG | 221178 |
rs2104256 | snp | C/T | 0.145978 | 0.227331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24109582 | GTGACAAGATAGAGA[C/T]AGAGGCAGAGGTAGA | 221178 |
rs2104257 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119603 | ACAGCTCTCTAAAGG[A/G]TCCTCAAAGGCAGCC | 221178 |
rs2104442 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978408 | tctagcaccactttt[C/T]tcttaaaatctcttt | 221178 |
rs2104443 | snp | A/G | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978427 | taaaatctctttgtg[A/G]taatgcagctacttc | 221178 |
rs2104444 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023753 | GCCAAGGAATGTGGG[C/T]GCCTCTCAAAGCTGG | 221178 |
rs2146682 | snp | A/G | 0.162581 | 0.234218 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179588 | actgaaactctgtac[A/G]gattaaatgcaagtc | 221178 |
rs2146683 | snp | A/G | 0.498277 | 0.0293024 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231341 | acatttcatagaaat[A/G]gaatcctgtaatacg | 221178 |
rs2146684 | snp | C/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24238228 | gtggcataatctcgg[C/G]tcactgcagtcttcg | 221178 |
rs2146685 | snp | A/G | 0.491316 | 0.0653198 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250596 | GTAACCCATAAAATT[A/G]TCTTAAAAGGGAACT | 221178 |
rs2146686 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115890 | cctcacctcatggat[C/G/T]tctcctgagcacagt | 221178 |
rs2146687 | snp | C/T | 0.3512 | 0.228601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126477 | GACAATTGTGTCTAT[C/T]CTGGAGTTTCCCTGG | 221178 |
rs2146688 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126599 | acaggttctgtcact[C/G]aggctggagtgcagt | 221178 |
rs2147992 | snp | C/G | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024099 | CTGAGTCATGTGCTG[C/G]GGAGGTCAGTGTGTC | 221178 |
rs2147993 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024326 | GGTGGGTGCTTAACT[A/G]TTTATtggatggatg | 221178 |
rs2147996 | snp | C/T | 0.394904 | 0.203722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000490 | GGATGGCAAGGGCTC[C/T]ATCTGCCCTGAAAGT | 221178 |
rs2147997 | snp | C/T | 0.395635 | 0.2032 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000429 | CCCCACCAAGAGCTG[C/T]CTGGCTTAGACACCT | 221178 |
rs2181504 | snp | G/T | 0.36021 | 0.224397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24126762 | CAGTCTCACTATGTT[G/T]CCCAGGCTGGTCTCA | 221178 |
rs2182221 | snp | A/T | 0.402806 | 0.197864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000047 | GGTTTTAATATGCAT[A/T]TTGGTGATAACTAAT | 221178 |
rs2182225 | snp | A/T | 0.217851 | 0.247924 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024379 | TGGATGGATGGATGG[A/T]TGGATAGATGGAATG | 221178 |
rs2182226 | snp | A/G | 0.499759 | 0.0109798 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025097 | tcctgtcttctttct[A/G]gaggtagccactgtt | 221178 |
rs2182228 | snp | A/G | 0.402982 | 0.197728 | intron-variant | SPATA13 | GRCh38.p7 | 13:24000547 | ATGTTGTTGCCGTGT[A/G]CTTGGTTTGTGGCCT | 221178 |
rs2209002 | snp | A/G | 0.386884 | 0.209196 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177660 | gagacagggtctcct[A/G]tgttgcccaggctgg | 221178 |
rs2209003 | snp | A/C | 0.387074 | 0.209071 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177744 | ggcatgagcctggcc[A/C]ttgggcctttttaat | 221178 |
rs2209507 | snp | A/G | 0.132066 | 0.220435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047422 | ctgcattcattttac[A/G]aaggcagtttcggtc | 221178 |
rs2244601 | snp | A/G | 0.497151 | 0.037632 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24160857 | CGGGGCTCCGCCGGC[A/G]CCGGAGGTGGCTCTG | 221178 |
rs2247174 | snp | C/G | 0.5 | 0.000399361 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990405 | GTGGAGTGTAGGAAG[C/G]AGGGGGCAATGAGCA | 221178 |
rs2248119 | snp | A/G | 0.39325 | 0.204889 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252956 | GGGTATCCAGTGAGC[A/G]CTTTGAAAATACAAA | 221178 |
rs2248122 | snp | A/C | 0.404733 | 0.196361 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998928 | aaaaaaaaaaaaaaa[A/C]caaagttagtgaaaa | 221178 |
rs2248349 | snp | A/G | 0.330016 | 0.236849 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24255078 | TTCAGCCAGGCCATT[A/G]GCTCCTAACCAGGAG | 221178 |
rs2248601 | snp | C/T | 0.241053 | 0.24984 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257317 | CAAAGGACGAATGCA[C/T]ACCCGTGCACCAAAG | 221178 |
rs2248602 | snp | C/T | 0.18325 | 0.240924 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257321 | GGACGAATGCACACC[C/T]GTGCACCAAAGTCAG | 221178 |
rs2248605 | snp | A/G | 0.379746 | 0.213696 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257329 | GCACACCCGTGCACC[A/G]AAGTCAGTCGATATG | 221178 |
rs2251368 | snp | A/G | 0.102014 | 0.201495 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172628 | tccttcttgcattca[A/G]ttggttttgcttctt | 221178 |
rs2252068 | snp | A/G | 0.271702 | 0.249056 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251215 | GCCTTCAGCTCCACA[A/G]ATCCTTACTGAGGGC | 221178 |
rs2255669 | snp | A/T | 0.433818 | 0.169443 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184659 | AGTGAGGAGTTTTGT[A/T]TTCTGTGCAGGACAA | 221178 |
rs2255675 | snp | C/T | 0.36606 | 0.221428 | intron-variant | SPATA13 | GRCh38.p7 | 13:24184917 | AAGCGACGGAGTCTA[C/T]GGAAAATGACCACTT | 221178 |
rs2255808 | snp | A/G | 0.495252 | 0.0484902 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186281 | TTGCAAAGCAAAAGT[A/G]GAAAATTAGAAGGTT | 221178 |
rs2255894 | snp | A/G | 0.331874 | 0.236213 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186599 | ATGCCACTGTGCTAG[A/G]CCCAAGAGCTAAAGA | 221178 |
rs2264961 | snp | C/T | 0.434687 | 0.168495 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172468 | tcttttgtgtttttt[C/T]ctaaaacgttcgtgg | 221178 |
rs2264962 | snp | C/G | 0.437401 | 0.165472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172552 | gcatgagatttaggt[C/G]agtgtttttttcttg | 221178 |
rs2264964 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231752 | caatttctcctcatc[C/T]ttgccaggacttggt | 221178 |
rs2265615 | snp | A/G | 0.115438 | 0.210697 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191101 | tgttaacatttttta[A/G]caatgaagtcttttt | 221178 |
rs2265616 | snp | C/T | 0.334642 | 0.235236 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191105 | aacattttttaacaa[C/T]gaagtctttttaaat | 221178 |
rs2265617 | snp | A/T | 0.485255 | 0.0845871 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191134 | attTATTAATTAAAT[A/T]AATtaattattattt | 221178 |
rs2265618 | snp | C/T | 0.193028 | 0.243422 | intron-variant | SPATA13 | GRCh38.p7 | 13:24191227 | acaatcctcctgcct[C/T]ggcctcccaaaatgt | 221178 |
rs2312603 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024696 | AACATATATATAATA[C/T]ATAACATTTTTATGT | 221178 |
rs2476208 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173425 | tcttgagattttcta[C/T]gtgggcaatcatgtc | 221178 |
rs2492086 | snp | C/T | 0.417196 | 0.185864 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987702 | AGCACATTCACATTA[C/T]TGTGCAACCTTCACC | 221178 |
rs2760355 | snp | A/T | 0.154661 | 0.231107 | intron-variant | SPATA13 | GRCh38.p7 | 13:24173794 | ctgaatcagtcttgg[A/T]tccctggaataaacc | 221178 |
rs2760356 | snp | C/T | 0.149999 | 0.229128 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177864 | taggatttcaacata[C/T]gaatttttttttaat | 221178 |
rs2760357 | snp | A/G | 0.188316 | 0.242271 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180177 | tattttgcatatggt[A/G]taagggaagatctca | 221178 |
rs2760358 | snp | A/G | 0.188946 | 0.24243 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180584 | ctgaatttgggatgc[A/G]ttgccattttaacaa | 221178 |
rs2760359 | snp | A/G | 0.477768 | 0.103061 | intron-variant | SPATA13 | GRCh38.p7 | 13:24186769 | GAAATGGGCAACAAC[A/G]CTATTGAGGCGGTTG | 221178 |
rs2760360 | snp | A/C | 0.332106 | 0.236133 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187414 | TCCACCCTTCTATTT[A/C]TAGAAGTTTGACAGG | 221178 |
rs2760361 | snp | A/T | 0.136166 | 0.22258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24187470 | cgttttattctgcct[A/T]gctttattgcatttt | 221178 |
rs2760362 | snp | A/G | 0.313814 | 0.241719 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188550 | agagaggtgaagaaa[A/G]gtttgaagctagtag | 221178 |
rs2760363 | snp | C/T | 0.313814 | 0.241719 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188569 | tgaagctagtagatg[C/T]gggttcttgaggttt | 221178 |
rs2760364 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197685 | GTCCTAGAGAATGAA[A/G]TCAGTTAGACTGGCT | 221178 |
rs2760365 | snp | G/T | 0.490063 | 0.0697833 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197696 | TGAAATCAGTTAGAC[G/T]GGCTTTGGTGTGATA | 221178 |
rs2760368 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24230235 | ACCACTCAACACCTG[C/G]TATGTGAACAGAAGG | 221178 |
rs2760371 | snp | A/G | 0.293294 | 0.246223 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246622 | CCCAGCACTTTGGGA[A/G]GCTGCAGTGGGTGGA | 221178 |
rs2760372 | snp | C/T | 0.334412 | 0.235318 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246634 | GGAAGCTGCAGTGGG[C/T]GGATCATGAGGTCAG | 221178 |
rs2760373 | snp | A/C | 0.409041 | 0.192888 | intron-variant, nc-transcript-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24252931 | GAGGTATCCAGTGAG[A/C]ACTTTATCTGGGTAT | 221178 |
rs2760374 | snp | C/T | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254458 | TCTCCCAGCTGCCTC[C/T]GTAACTTCATTTTTA | 221178 |
rs2760375 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256521 | TAAGTAGTATCCACA[A/G]CTAAATTTTTCTCAA | 221178 |
rs2760376 | snp | C/G | 0.242201 | 0.249878 | intron-variant | SPATA13 | GRCh38.p7 | 13:24256966 | TGGGGAATTATCTTT[C/G]CCGCCTTTGCTTTGC | 221178 |
rs2760377 | snp | C/T | 0.153665 | 0.230694 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159973 | AGGGTTTGCTTCTCT[C/T]CTGTGGTTTTCATGT | 221178 |
rs2760378 | snp | C/G | 0.142609 | 0.225759 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160115 | AAAAATCCCTACCCT[C/G]CGTTTTCCTTTCACA | 221178 |
rs2765140 | snp | A/T | 0.0425829 | 0.139564 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978141 | actcctaacttcaag[A/T]gatccacctgtctcg | 221178 |
rs2765141 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978190 | attacaagcgtgagc[C/T]actgggcacctggcc | 221178 |
rs2765142 | snp | G/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978289 | attccattgactttt[G/T]agtgtgtccgttttc | 221178 |
rs2765144 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978699 | TCTCCTAACATTCTC[C/T]Atttgtctttttttg | 221178 |
rs2765145 | snp | C/G/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978863 | ccacacccaactaat[C/G/T]aaaaaaatttttttt | 221178 |
rs2765146 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979221 | atctgctaaagttca[C/T]gtgttggaaacttga | 221178 |
rs2765147 | snp | A/G | 0.440471 | 0.161928 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986633 | AAAGTCTGCCTGGGA[A/G]AATGTTTAGAGGTGT | 221178 |
rs2765148 | snp | A/C | 0.421684 | 0.181726 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986659 | GGTGTGGATTTCTCA[A/C]CTTTAATTTATCTTT | 221178 |
rs2765149 | snp | A/G | 0.030278 | 0.119257 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987151 | ATGAGACATTCATTT[A/G]TAATGAAAGCAGATC | 221178 |
rs2765150 | snp | A/T | 0.499816 | 0.0095829 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987192 | TGGGATGGATAATCT[A/T]GGGGTCTTATTTAGC | 221178 |
rs2765152 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988838 | GTTGGGTTTTTCTCC[C/T]CCCTCTTCTTTATAT | 221178 |
rs2765153 | snp | G/T | 0.5 | 0.00019968 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989140 | AATGTTAAGATTTAC[G/T]TGGCTGGGCGCGGTG | 221178 |
rs2765154 | snp | G/T | 0.499999 | 0.000798721 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990007 | AATATCTGTTGTTTA[G/T]AAGCCACCCAGGTTA | 221178 |
rs2765155 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990010 | ATCTGTTGTTTATAA[A/G]CCACCCAGGTTATGG | 221178 |
rs2765156 | snp | A/C | 0.498734 | 0.0251279 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991595 | CTTTGCTATTACTGC[A/C]TTCTTTTCTCCAATG | 221178 |
rs2765158 | snp | A/G | 0.495368 | 0.0478996 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995168 | AGCCTGAAGATACAT[A/G]CCAATCTCATTTGCT | 221178 |
rs2765159 | snp | G/T | 0.495407 | 0.0477027 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995287 | TGATCTTTGAACACA[G/T]GTAAATCAAAGACAA | 221178 |
rs2765160 | snp | G/T | 0.383824 | 0.211166 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995352 | GTGATGAATCCCATT[G/T]AACGGGATTTGACAT | 221178 |
rs2765161 | snp | G/T | 0.420415 | 0.182917 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996640 | TGAGATTTGGCTACT[G/T]ATTAAAAGAGTAGCT | 221178 |
rs2765162 | snp | A/G | 0.41141 | 0.19091 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996931 | tggccctctcagatc[A/G]tcttggaGGCAGGGG | 221178 |
rs2765163 | snp | A/G | 0.408188 | 0.193589 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997083 | ATCACTCTTGTAAGG[A/G]TCAGTCACGATTGAT | 221178 |
rs2765164 | snp | C/T | 0.410061 | 0.192043 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997187 | AGCAGAAATGGTTTC[C/T]ATTTTTATCTTTTCT | 221178 |
rs2765165 | snp | A/T | 0.409552 | 0.192466 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997511 | atgtatcactagttc[A/T]tggcttttcattgct | 221178 |
rs2765166 | snp | A/G | 0.409552 | 0.192466 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997594 | ggtaatttataaaga[A/G]gaggtttatttggct | 221178 |
rs2765167 | snp | C/T | 0.398174 | 0.201356 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997871 | gagccaaacacttcc[C/T]actaggccccatctc | 221178 |
rs2765168 | snp | C/T | 0.396 | 0.202938 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997910 | gggatcatatttgaa[C/T]atcagtcttggaggg | 221178 |
rs2765169 | snp | G/T | 0.417521 | 0.185571 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998416 | tgtccatttttatca[G/T]gttgttttcatgtta | 221178 |
rs2765170 | snp | A/G | 0.400682 | 0.199487 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998428 | tcaggttgttttcat[A/G]ttattgcagttgaga | 221178 |
rs2765171 | snp | G/T | 0.399968 | 0.200024 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998437 | tttcatgttattgca[G/T]ttgagagtgttttat | 221178 |
rs2765172 | snp | C/T | 0.399611 | 0.200291 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998625 | gatcgtgattttttg[C/T]tgtatttgtgaaatc | 221178 |
rs2765173 | snp | A/G | 0.399611 | 0.200291 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998633 | ttttttgctgtattt[A/G]tgaaatcttttccta | 221178 |
rs2765174 | snp | A/G | 0.403334 | 0.197456 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999691 | gtttctgcctctcag[A/G]gattactctcaagtc | 221178 |
rs2765175 | snp | G/T | 0.399073 | 0.200692 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999866 | CTATTTAGATACTTA[G/T]GCAAAGCAAATGCAA | 221178 |
rs2765176 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24005690 | GCTGGTATGTGTCAT[A/G]TAAAGGGTCAGAGAA | 221178 |
rs2765181 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24010764 | ACCCAAGGCCTGGAT[A/G]GTGTCTTGGCAAGCA | 221178 |
rs2793482 | snp | A/G | 0.470908 | 0.117046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185945 | GGCCTTAAGATTGCC[A/G]TAAGATTCAAGCCTA | 221178 |
rs2793483 | snp | C/T | 0.471004 | 0.116864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185549 | ATTATGTCAAAATTA[C/T]AGAAGGCTATTAATG | 221178 |
rs2793484 | snp | A/G | 0.442926 | 0.158996 | intron-variant | SPATA13 | GRCh38.p7 | 13:24185159 | ATACGTCACAGGGGA[A/G]CTTCAGGGCTTATGA | 221178 |
rs2793485 | snp | C/G | 0.499866 | 0.0081858 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162201 | AAGGAGATGGGAGAA[C/G]TGGGTGGAGGCAGAT | 221178 |
rs2793486 | snp | C/T | 0.131723 | 0.220251 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160003 | TTGTGAGGCTCAAGG[C/T]CTAATCATTAATTGA | 221178 |
rs2793488 | snp | G/T | 0.459801 | 0.135955 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246585 | GTGACTCAGGCCGGG[G/T]GTGGTGGCTCACGCC | 221178 |
rs2793489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:24248787 | AGAACAGCAGTGGAT[A/G]GCATTACCCATTCAT | 221178 |
rs2793490 | snp | A/G | 0.223819 | 0.248625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24250798 | GTCTGAAGGTGCTCC[A/G]CTGTTGGGAAATGAT | 221178 |
rs2793491 | snp | C/T | 0.359023 | 0.224975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251913 | ATGGGCCCATCTGAC[C/T]GTTTCCAGCTAACCT | 221178 |
rs2810687 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23978824 | cctcaaccactggag[C/T]agctggagtacaagc | 221178 |
rs2810688 | snp | A/G | 0.0422008 | 0.138995 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979486 | AACAGTAAGGGGTTG[A/G]GAGAAGGGAGAGAAA | 221178 |
rs2810689 | snp | A/G | 0.0337553 | 0.125452 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979776 | GCCCTGGCCGAGGAA[A/G]TGAAGAGGGCGCAGG | 221178 |
rs2810690 | snp | A/C/G | 0.0445584 | 0.142804 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979852 | CGTGACCTTCCTCCC[A/C/G]CTTCCAGCTCGGAGC | 221178 |
rs2810691 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984450 | CTCTTCTCTGTAAGT[C/T]GAATAGAAACCGTGT | 221178 |
rs2810692 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984644 | CTGAAGAGCAGGGCT[C/G]CAATGCACCTGGTGG | 221178 |
rs2810693 | snp | A/G | 0.424037 | 0.179474 | intron-variant | SPATA13 | GRCh38.p7 | 13:23985205 | TTGAGTGGCTTGGAA[A/G]TTCAAACCACTCAAC | 221178 |
rs2810694 | snp | C/T | 0.499154 | 0.0205497 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986663 | TGGATTTCTCACCTT[C/T]AATTTATCTTTTTGG | 221178 |
rs2810695 | snp | C/T | 0.410568 | 0.191619 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987863 | attctatagtatttg[C/T]cctttagtatctggc | 221178 |
rs2810696 | snp | C/G | 0.436692 | 0.166271 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988811 | TTCCTTTGTTCATTT[C/G]TCAGTCGGGCTGTTG | 221178 |
rs2810697 | snp | C/T | 0.195526 | 0.243993 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989756 | AAATCTAACCCCCAA[C/T]GTGATGGTATCAGAA | 221178 |
rs2810698 | snp | C/T | 0.421684 | 0.181726 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989889 | TATGTGAGGATGCAG[C/T]GAGATGGTACCATCT | 221178 |
rs2810699 | snp | A/C | 0.499793 | 0.0101816 | intron-variant | SPATA13 | GRCh38.p7 | 13:23992017 | TACTACAAGCCAAGC[A/C]CTCTGCTAAATATTT | 221178 |
rs2810700 | snp | A/G | 0.420574 | 0.182769 | intron-variant | SPATA13 | GRCh38.p7 | 13:23993233 | AACTGCAGAATCACA[A/G]CTGCTGCCTCAGAGC | 221178 |
rs2810701 | snp | A/C | 0.409382 | 0.192607 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997645 | aggaagcatcagacc[A/C]gcatctgcttctgtt | 221178 |
rs2810702 | snp | C/T | 0.397994 | 0.201489 | intron-variant | SPATA13 | GRCh38.p7 | 13:23998151 | taccaaactgttttc[C/T]gaagtctttgcacca | 221178 |
rs2810703 | snp | C/T | 0.385168 | 0.210309 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999483 | tcttccaacccatca[C/T]acagtctatctctca | 221178 |
rs2810704 | snp | C/G | 0.403334 | 0.197456 | intron-variant | SPATA13 | GRCh38.p7 | 13:23999669 | aagccaaaggctcag[C/G]gtatttgtttctgcc | 221178 |
rs2861540 | snp | A/C | 0.429087 | 0.174436 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221872 | TGAGCCAAGATTGCG[A/C]CACTGCACTCCAAAC | 221178 |
rs2861541 | snp | A/T | 0.378174 | 0.214642 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221487 | GAAAAATGAAAATCC[A/T]GCTCCCCCTTAACCT | 221178 |
rs2861542 | snp | A/T | 0.377977 | 0.21476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221484 | AAATGAAAATCCTGC[A/T]CCCCCTTAACCTTTC | 221178 |
rs2861543 | snp | A/C | 0.383439 | 0.21141 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208708 | ATGGAACTGTCAGGG[A/C]TTTCTTTTGGCCTAT | 221178 |
rs2861544 | snp | C/T | 0.383439 | 0.21141 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208702 | CTGTCAGGGATTTCT[C/T]TTGGCCTATGGGCTC | 221178 |
rs2861545 | snp | A/G | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208591 | TGCAACTAAAGATCA[A/G]TCTGGAAAGTCCCCA | 221178 |
rs2861546 | snp | A/G | 0.213333 | 0.247296 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204610 | tggggtctgggagga[A/G]gaggagaaatgggag | 221178 |
rs2861547 | snp | G/T | 0.319856 | 0.240042 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052076 | GCACAGGATGCTGGT[G/T]TAAGAAGCCAAACCC | 221178 |
rs2861548 | snp | A/G | 0.488057 | 0.0763479 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050029 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCACCT | 221178 |
rs2861549 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050023 | TAGCTGGGCGTGGTG[A/G]TGGGCACCTGTAATC | 221178 |
rs2861550 | snp | A/G | 0.276267 | 0.248616 | intron-variant, utr-variant-5-prime | SPATA13 | GRCh38.p7 | 13:24270718 | CTGCTTTGACGTTGT[A/G]TGCGTTCCCGGCCAG | 221178 |
rs2861551 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288565 | GGTGGAATCCTTGGG[C/T]AAGAGGAATCCTTGC | 221178 |
rs2861552 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288566 | GTGGAATCCTTGGGT[A/T]AGAGGAATCCTTGCC | 221178 |
rs2861553 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288567 | TGGAATCCTTGGGTA[A/G]GAGGAATCCTTGCCC | 221178 |
rs2861554 | snp | A/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288569 | GAATCCTTGGGTAAG[A/T]GGAATCCTTGCCCTG | 221178 |
rs2862241 | snp | A/G | 0.420415 | 0.182917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24180585 | attgttaaaatggca[A/G]tgcatcccaaattca | 221178 |
rs2862243 | snp | C/T | 0.477853 | 0.102875 | intron-variant | SPATA13 | GRCh38.p7 | 13:24179310 | tgagttaccatttga[C/T]tcagcaatgccacgc | 221178 |
rs2862244 | snp | A/G | 0.351418 | 0.228505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131997 | tgaccttggtcacac[A/G]gtcaaccctagctgc | 221178 |
rs2862245 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087034 | CCACTGTTTCTCCAC[A/G]ATTGCTGTTCTGCTT | 221178 |
rs2862246 | snp | C/T | 0.494976 | 0.0498674 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082903 | CCATACTGAGACGAT[C/T]TAGAAGTTTTTCTTA | 221178 |
rs2862247 | snp | A/G | 0.185788 | 0.241613 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082776 | GCGGACTGCAGTGGC[A/G]CAATCTCGGCTCACT | 221178 |
rs2862248 | snp | A/G | 0.491577 | 0.0643472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068660 | atgcaagtcaaaata[A/G]tccaaaaataacaga | 221178 |
rs2901979 | snp | C/G | 0.153332 | 0.230554 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208453 | TATATTCACTCACTG[C/G]AGTGCTAGGAGCACT | 221178 |
rs2901980 | snp | A/T | 0.428635 | 0.174898 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266372 | CCTTGAGCCCAGGAG[A/T]TCGAGGCTGCAGTGA | 221178 |
rs2901981 | snp | A/G | 0.161267 | 0.233723 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294000 | GGATGGTTGGTCTCC[A/G]TGGCCCCGCATTATT | 221178 |
rs2902187 | snp | C/T | 0.488485 | 0.0749998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24096210 | agactataagctcca[C/T]gtgaacatgggctat | 221178 |
rs2902188 | snp | C/T | 0.247905 | 0.249991 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060483 | tgcctaggttgtctt[C/T]cagggtttagatagc | 221178 |
rs3067220 | in-del | -/TT/TTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24258365 | ttttttttttttttt[-/TT/TTT]GAGATGAACTCTTCA | 221178 |
rs3067223 | in-del | -/TA | 0.0123036 | 0.0774623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24231173 | agctccataaacata[-/TA]aaaatcactgaattg | 221178 |
rs3067259 | in-del | -/CACCCCC | 0.386504 | 0.209444 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208576 | GTCTGGAAAGTCCCC[-/CACCCCC]ACCAGTCTTCTTGAT | 221178 |
rs3067263 | in-del | -/A/AA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198951 | AAAAAAAAAAAAAAA[-/A/AA]GATTTTATAGTTCTA | 221178 |
rs3067264 | in-del | -/AA | 0.322007 | 0.239405 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052073 | ACAGGATGCTGGTGT[-/AA]GAAGCCAAACCCTGC | 221178 |
rs3067301 | in-del | -/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24285681 | GCCACCACATCTGGC[-/T]TTTTTTTTTTTTTTT | 221178 |
rs3075288 | in-del | -/TT/TTT | 0.494143 | 0.0537956 | intron-variant | SPATA13 | GRCh38.p7 | 13:24141173 | CCTAATTTCTTTTTC[-/TT/TTT]TTTTTTTTTTTTGAG | 221178 |
rs3075291 | in-del | -/GT | 0.389527 | 0.207442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112554 | TGTGTGTGTGTGTGT[-/GT]ATGCCTGGCACAAGA | 221178 |
rs3075296 | in-del | -/TTTTT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24082826 | ttttttttttttttt[-/TTTTT]gagacggagtctcgc | 221178 |
rs3075322 | in-del | -/TGGATT | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060706 | gttccttacagatgc[-/TGGATT]tggatattagacctt | 221178 |
rs3077626 | in-del | -/AGA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24011901 | CTGCAAGTTTAAAGA[-/AGA]AGGCTGAGCATTCTG | 221178 |
rs3078774 | in-del | -/T | 0.353587 | 0.22753 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981272 | TTGACATTTTTTTTT[-/T]CCTATGGTATATGGC | 221178 |
rs3222505 | microsatellite | (CA)16/17/18/19/20/21/22/23 | 0.78355 | 0.0675881 | intron-variant | SPATA13 | GRCh38.p7 | 13:24233926 | CTTTATACACTTAAA[(CA)16/17/18/19/20/21/22/23]TGATAAGATTATTTC | 221178 |
rs3742176 | snp | C/T | 0.225597 | 0.248806 | intron-variant | SPATA13 | GRCh38.p7 | 13:24273173 | GTCGTTGGCTCTGGG[C/T]TTCTTTGTATCTTGC | 221178 |
rs3803218 | snp | A/G | 0.31014 | 0.242659 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304328 | ATATAACTTTTAACT[A/G]TGTCTAGAGAAGGCA | 221178 |
rs3803219 | snp | A/C | 0.35207 | 0.228214 | utr-variant-3-prime, upstream-variant-2KB | SPATA13, C1QTNF9 | GRCh38.p7 | 13:24305174 | TATTCATGGGTAATG[A/C]AGAAATGGTTTGCAT | 221178 |
rs3915936 | snp | C/T | 0.485596 | 0.0836329 | intron-variant | SPATA13 | GRCh38.p7 | 13:24283739 | CTTGCAGATAAAGGA[C/T]GGAAGCAGAATATTG | 221178 |
rs3927452 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238065 | ACACA[G/T] | 221178 |
rs3939716 | snp | A/T | 0.177182 | 0.23916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204665 | tctacaaatttgact[A/T]ctctaggtacttcaa | 221178 |
rs3979306 | snp | C/T | 0.499954 | 0.00479211 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111918 | GCAGTATAACCTCAA[C/T]ACCAACATCAAACAA | 221178 |
rs3979679 | snp | A/C/G/T | | | intron-variant | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254200 | GTTCACAGTGAATCA[A/C/G/T]AGGCCACAGTGAATC | 221178 |
rs4067474 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23992111 | TGGTTCTGGATCTCA[A/G]AAATCTCACTGCAAA | 221178 |
rs4067476 | in-del | -/CA/CACA/CACACA | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23987001 | acacacacacacaca[-/CA/CACA/CACACA]NNNGATATATCCATT | 221178 |
rs4129558 | snp | A/C | 0.203882 | 0.245709 | intron-variant | SPATA13 | GRCh38.p7 | 13:24112493 | CTACTTCCGTGGCTG[A/C]GCATGAGAATTCAAC | 221178 |
rs4145023 | snp | A/C | 0.416708 | 0.186302 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281250 | ACTCCTCCCCCTCCA[A/C]CCCCGTCTCTTGGTC | 221178 |
rs4238175 | snp | A/G | 0.110519 | 0.207473 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276185 | tcacaatagccaagt[A/G]gtaaaaggagcccaa | 221178 |
rs4261384 | snp | A/G | 0.463234 | 0.130503 | intron-variant | SPATA13 | GRCh38.p7 | 13:24240217 | ATGAGCCGTGATTGC[A/G]CCACTGCACTGCAGC | 221178 |
rs4288857 | snp | A/G | 0 | 0 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304062 | GTCCTTAGCAATGAA[A/G]TCACAAAGACAGCCA | 221178 |
rs4296126 | snp | C/T | 0.45843 | 0.138046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095796 | GTGTTGCAATCCCAG[C/T]GAAGTGCTTTGGATT | 221178 |
rs4303330 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | SPATA13 | GRCh38.p7 | 13:24172012 | CAAGACTGTACTACA[A/G]TGGTGGAACTAAGGA | 221178 |
rs4304896 | snp | G/T | 0.137527 | 0.223271 | intron-variant | SPATA13 | GRCh38.p7 | 13:24035748 | gctgagcgaggtggc[G/T]cacacctgttctccc | 221178 |
rs4332615 | snp | C/G | 0.279461 | 0.248258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266109 | GTGCTGACTACTGTT[C/G]TGAGTTTGAGATACT | 221178 |
rs4347484 | snp | A/C | 0.414905 | 0.187899 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154212 | tgggtaaatacccaa[A/C]aagagtgtgattttt | 221178 |
rs4399412 | snp | A/G | 0.461703 | 0.132974 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154490 | tttatggcaataaac[A/G]ttaatgtttaccttt | 221178 |
rs4462447 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025961 | aggcatatagcacca[C/T]gcctggctaattttt | 221178 |
rs4465466 | snp | G/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026242 | TGATTAATGCTTCTT[G/T]TGAGTTAAGAAATCC | 221178 |
rs4465467 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221884 | GTGTCGCAATCTTGG[A/C]TCACTGCAACTTCTG | 221178 |
rs4470012 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026321 | TTTGGAGTTTTGTGT[C/T]CTTCACATGAAGAGC | 221178 |
rs4470013 | snp | C/T | 0.198014 | 0.244535 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065684 | AATAGATGGAATTAA[C/T]ACTAGAATCACATGG | 221178 |
rs4503645 | snp | A/T | 0.123798 | 0.215808 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092945 | ATCTTCTCATTAACG[A/T]TGCAGATGACTATTT | 221178 |
rs4511384 | snp | C/T | 0.454664 | 0.143571 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188105 | tagctctttgggagg[C/T]caaggcgggcagatt | 221178 |
rs4542512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24298127 | CACTTTGGATGCCAC[A/C]TGCAGGGTATGAAGA | 221178 |
rs4562938 | snp | C/G | 0.307176 | 0.243374 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095821 | TGGATTGGTTCAGCT[C/G]TAAAAACCGTCATTT | 221178 |
rs4569111 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111185 | AAAGAGGCCAGATAC[A/G]TGCATGAGCCACCAC | 221178 |
rs4624011 | snp | C/T | 0.386313 | 0.209568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24177515 | ttttagacacagtct[C/T]actctgcaatcgtag | 221178 |
rs4628803 | snp | C/G | 0.402806 | 0.197864 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154509 | atgtttacctttggg[C/G]tactgggcattgcta | 221178 |
rs4638422 | snp | C/T | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026066 | cctcggccttctaaa[C/T]ACCttttctttttac | 221178 |
rs4640031 | snp | A/G | 0.299916 | 0.244966 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095776 | AACCATCCTGTCCCA[A/G]ACAAGTGTTGCAATC | 221178 |
rs4644724 | snp | C/T | 0.422315 | 0.181128 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154166 | CAGAAGGTAAACATA[C/T]GCACACCTGATAGTC | 221178 |
rs4644725 | snp | C/T | 0.413748 | 0.188909 | intron-variant | SPATA13 | GRCh38.p7 | 13:24154182 | GCACACCTGATAGTC[C/T]GGCAGTACCACTCCT | 221178 |
rs4769297 | snp | C/T | 0.308414 | 0.24308 | intron-variant | SPATA13 | GRCh38.p7 | 13:23982926 | CTCTCCCTCACCTCC[C/T]CAAGGCTGCTCTGCC | 221178 |
rs4769298 | snp | A/T | 0.45235 | 0.146814 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983109 | AATGGGAGTGAGGGG[A/T]TGGGAGAGAGTGTCT | 221178 |
rs4769299 | snp | G/T | 0.311859 | 0.242226 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987408 | GATGGTGGAGTTATA[G/T]TCTTTGGAGAAAAGT | 221178 |
rs4769301 | snp | A/G | 0.306431 | 0.243548 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997661 | gcatctgcttctgtt[A/G]aggcctcaggaagct | 221178 |
rs4769303 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | SPATA13 | GRCh38.p7 | 13:24002565 | TCAGGGGGGTGAGTG[C/T]GTTGGTCTTTGAGTC | 221178 |
rs4769304 | snp | A/G | 0.483345 | 0.0897213 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016913 | CATGCCCAGCCTTCA[A/G]TGAATACAGTTTTAG | 221178 |
rs4769305 | snp | C/T | 0.386313 | 0.209568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018309 | GTCAAAATGTCTTTT[C/T]TGATGGACAAATAGA | 221178 |
rs4769306 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | SPATA13 | GRCh38.p7 | 13:24018323 | TTTGATGGACAAATA[A/G]AAATGTTGCAAAAGA | 221178 |
rs4769307 | snp | A/G | 0.499767 | 0.0107802 | intron-variant | SPATA13 | GRCh38.p7 | 13:24023846 | ACCTGCGAGACCCCT[A/G]TTGAACTTCCACCCT | 221178 |
rs4769308 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026726 | GGGACTACAGGTGCC[C/T]GCCACCACGTCCAGC | 221178 |
rs4769309 | snp | A/G | 0.307671 | 0.243257 | intron-variant | SPATA13 | GRCh38.p7 | 13:24036921 | GCTGAGACTACAGGC[A/G]TGCACCACCATGCCC | 221178 |
rs4769310 | snp | A/G | 0.452473 | 0.146644 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037027 | gatctgcccacttca[A/G]tctcccaaagtgctg | 221178 |
rs4769311 | snp | A/G | 0.41141 | 0.19091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037256 | ATACCTAATGTAAAT[A/G]ACGAGTTAATGGGTG | 221178 |
rs4769312 | snp | A/G | 0.499885 | 0.00758699 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049081 | AAAAAGATAAGAAAT[A/G]TCTAAAGTCTTCTAA | 221178 |
rs4769313 | snp | A/G | 0.497387 | 0.0360476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24049249 | GATGCCTCGCCTACA[A/G]GACAGCAGCCCCATG | 221178 |
rs4769314 | snp | A/G | 0.489608 | 0.0713316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050800 | TGGCCAAGGTGCCTC[A/G]TGCCACCCACCACGT | 221178 |
rs4769315 | snp | C/G | 0.493432 | 0.0569306 | intron-variant | SPATA13 | GRCh38.p7 | 13:24054004 | CCTCTGTGTCGTTGG[C/G]GTGACGGAGGCTCCT | 221178 |
rs4769316 | snp | A/G | 0.33303 | 0.235809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074452 | TGGCTATTGTGAATA[A/G]TATGGCTATGAACCT | 221178 |
rs4769317 | snp | C/G | 0.326035 | 0.238157 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098083 | TATTAAAGACCAGGC[C/G]CCAGAGAAAAACAAA | 221178 |
rs4769322 | snp | A/G | 0.369958 | 0.21934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122229 | TTCTTTGTTCTTCAG[A/G]AAGATGGTGAGTCAG | 221178 |
rs4769323 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122353 | TTAAATATCTGATAC[A/G]CATCAACAGGGTTAT | 221178 |
rs4769324 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133401 | CTCTGTGTATTTAAA[C/T]GTTGTAAATTTCAGT | 221178 |
rs4769326 | snp | C/T | 0.440884 | 0.161442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139842 | GGAGGCCAAGGAGGG[C/T]GGATAACGAGGTCAG | 221178 |
rs4769327 | snp | A/C | 0.46974 | 0.119223 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147815 | TTTTCTGAGCTTGAC[A/C]GCTCTAGATACCTCA | 221178 |
rs4769329 | snp | C/T | 0.472429 | 0.114129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153762 | GTCATTTTGAAATAT[C/T]CATGGAGATTGATGA | 221178 |
rs4769330 | snp | C/T | 0.452719 | 0.146304 | intron-variant | SPATA13 | GRCh38.p7 | 13:24157104 | AGACCTTAAGTTACT[C/T]CCTCCAGGTGAAAGT | 221178 |
rs4769331 | snp | A/G | 0.439224 | 0.163383 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24158988 | TATAAAAAGTATTGC[A/G]TGTAAATGTTAATAG | 221178 |
rs4769332 | snp | C/T | 0.24134 | 0.24985 | intron-variant, downstream-variant-500B | SPATA13, MIR2276 | GRCh38.p7 | 13:24162953 | CACCAGTGGAGGACA[C/T]GAATTCTATACCTGT | 221178 |
rs4769333 | snp | A/G | 0.242488 | 0.249887 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163082 | CCCTCTTAGCCACAG[A/G]AAGCCCTGAAGAAAG | 221178 |
rs4769334 | snp | A/T | 0.379746 | 0.213696 | intron-variant | SPATA13 | GRCh38.p7 | 13:24176411 | CTTTTCATGTAATCT[A/T]TACAGAAAAGTTGGA | 221178 |
rs4769335 | snp | A/G | 0.451732 | 0.147663 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188818 | agagcttcaaaggac[A/G]caatgattctccggt | 221178 |
rs4769337 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232553 | ttttttaatattttt[C/T]ttttttgagacaggg | 221178 |
rs4769338 | snp | A/G | 0.41141 | 0.19091 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241042 | ATTACTGACATGCAT[A/G]TCACCCCATTCCGTA | 221178 |
rs4769339 | snp | C/G | 0.270892 | 0.249126 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279507 | ctgctggagggagcc[C/G]gaagctggatgggaa | 221178 |
rs4770535 | snp | A/G | 0.308661 | 0.24302 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983174 | GGGGGCTTAAGTGAC[A/G]GACCTTGATTGTCCC | 221178 |
rs4770536 | snp | G/T | 0.308661 | 0.24302 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983205 | AGTGCTGGGGGCTGG[G/T]AGTCCGAGATCAAGG | 221178 |
rs4770537 | snp | A/G | 0.307423 | 0.243316 | intron-variant | SPATA13 | GRCh38.p7 | 13:23986192 | TCGCCCAGGGACCTA[A/G]TCATTGTATAACCTC | 221178 |
rs4770539 | snp | A/T | 0.307423 | 0.243316 | intron-variant | SPATA13 | GRCh38.p7 | 13:23989060 | TTACTGAAATGGTTC[A/T]TATGCTGAAGAAAGA | 221178 |
rs4770541 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996245 | gagggagagtccgcc[G/T]ccttgcctttccacc | 221178 |
rs4770545 | snp | C/T | 0.383053 | 0.211653 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006064 | GCCGGAGGTGCCTGC[C/T]GTGTTCCTGCAGTTT | 221178 |
rs4770546 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006401 | AAAATCTGTACACAG[C/T]ATAAATGAGCAACGG | 221178 |
rs4770548 | snp | G/T | 0.139564 | 0.224285 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015240 | ACTCTTAACGAGAGA[G/T]GAATAGATACAAAAA | 221178 |
rs4770549 | snp | A/G | 0.434398 | 0.168811 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017540 | TATACACACATATGT[A/G]TATATACATTTTTGT | 221178 |
rs4770550 | snp | A/G | 0.185472 | 0.241529 | intron-variant | SPATA13 | GRCh38.p7 | 13:24017560 | TACATTTTTGTTTAC[A/G]TATATTTTTTAGATC | 221178 |
rs4770551 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020183 | AGGAATTTGGATTTT[G/T]TTGAGATCTGTGTGT | 221178 |
rs4770552 | snp | C/T | 0.362941 | 0.223034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24020291 | AGAGTGCTTGAACTT[C/T]TAACCAATATGCAGT | 221178 |
rs4770553 | snp | C/T | 0.41275 | 0.189769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021856 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 221178 |
rs4770554 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026771 | tttagtggagacggg[G/T]tttcaccgtgttagc | 221178 |
rs4770555 | snp | C/T | 0.412917 | 0.189626 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027612 | AGTTGCTGTTTTTTA[C/T]CTTTATGTATTAGTT | 221178 |
rs4770556 | snp | A/G | 0.41275 | 0.189769 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027621 | TTTTTATCTTTATGT[A/G]TTAGTTCTTAGTTCA | 221178 |
rs4770557 | snp | A/G | 0.482831 | 0.0910472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030824 | ACCATATTGCCAGCA[A/G]TGGAAAAGACCTTTA | 221178 |
rs4770558 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038193 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 221178 |
rs4770559 | snp | G/T | 0.0733688 | 0.176922 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042773 | CCTCACTTGGTCAGC[G/T]GTGGAGCCCAAGAAT | 221178 |
rs4770560 | snp | A/G | 0.364609 | 0.222182 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048704 | AGATAAATAAATTGT[A/G]TAAAGACCCAAGCTG | 221178 |
rs4770563 | snp | A/C | 0.4983 | 0.0291038 | intron-variant | SPATA13 | GRCh38.p7 | 13:24058911 | GTAATGATGCCAACT[A/C]TGTCTCATGTAGACC | 221178 |
rs4770564 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SPATA13 | GRCh38.p7 | 13:24059133 | CCCACCACCATGTCC[C/T]GCTAATTTTTTGTAT | 221178 |
rs4770567 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069301 | tctgatttatttgag[C/T]agtggtttgtagttc | 221178 |
rs4770568 | snp | C/T | 0.330947 | 0.236533 | intron-variant | SPATA13 | GRCh38.p7 | 13:24073434 | TATACCTATCTGTCA[C/T]ATGTTAGAAATTTGA | 221178 |
rs4770569 | snp | A/G | 0.194902 | 0.243853 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074304 | tttatttaactcaag[A/G]ttcatccacgtggta | 221178 |
rs4770570 | snp | A/G | 0.19459 | 0.243782 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074377 | ttctgttgtatgaat[A/G]gaccacatttttttt | 221178 |
rs4770571 | snp | A/G | 0.498277 | 0.0293024 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074698 | TGAATCCTGGTGGCC[A/G]ttgaaagaaaaactt | 221178 |
rs4770573 | snp | A/G | 0.33303 | 0.235809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086248 | TTTTAGTGTAAGTGT[A/G]TCATTCATATTGCAT | 221178 |
rs4770574 | snp | C/T | 0.331179 | 0.236453 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086317 | GCTTTCACTGGGTGT[C/T]CTGTGCTTTATCTGG | 221178 |
rs4770575 | snp | A/G | 0.330482 | 0.236691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086375 | GTTTTGTGATCGCAG[A/G]GTCCTCTTAGGAGGA | 221178 |
rs4770580 | snp | A/C | 0.2462 | 0.249971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24097747 | ATGTAAGGAGAGGGA[A/C]CCCCCAACATAGCCA | 221178 |
rs4770585 | snp | A/G | 0.381697 | 0.212499 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118334 | AAAAATGCCACATGT[A/G]CAAAATTGCTTATGC | 221178 |
rs4770586 | snp | A/G | 0.382085 | 0.212258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118448 | GAATTCCTAAGCACC[A/G]GAAGCTCAATTCACT | 221178 |
rs4770587 | snp | C/T | 0.370365 | 0.219117 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118696 | AGCAGGACTGCATCA[C/T]TGTGTTTCTTAGGGA | 221178 |
rs4770591 | snp | G/T | 0.49995 | 0.00499176 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122331 | TTGAATAGTTTGAAA[G/T]ATAGCTTTAAATATC | 221178 |
rs4770592 | snp | C/T | 0.3746 | 0.216737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122526 | TTCATCACTCCCCGG[C/T]TCCTCTGGTCAGTGC | 221178 |
rs4770593 | snp | A/G | 0.375598 | 0.21616 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122545 | TCTGGTCAGTGCCAC[A/G]CCCTTTGCACTGCAG | 221178 |
rs4770594 | snp | A/G | 0.244205 | 0.249933 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122681 | GACAGACAGAAGTGT[A/G]TCTGTATCAACTGTT | 221178 |
rs4770595 | snp | A/G | 0.3746 | 0.216737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24122715 | TAATTACGAAGGAGG[A/G]GCATCATATCTGTAA | 221178 |
rs4770596 | snp | C/T | 0.347914 | 0.230028 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133303 | GTGAGATTAAGTTCA[C/T]CTGGTAGAGATTGTG | 221178 |
rs4770597 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133327 | GATTGTGTAAGCCCA[A/G]TTGGAAATAGTGGCT | 221178 |
rs4770598 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133338 | CCCAGTTGGAAATAG[C/T]GGCTCCTGGGACATT | 221178 |
rs4770599 | snp | C/T | 0.35809 | 0.225425 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134825 | TCCCCCAAAATTTTG[C/T]ATGTTGAAGTCCTAA | 221178 |
rs4770600 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134829 | CCAAAATTTTGCATG[C/T]TGAAGTCCTAATTTC | 221178 |
rs4770601 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135972 | TTTAAGTGAATCTTT[C/T]GATCTCCTGGAAACA | 221178 |
rs4770602 | snp | C/G | 0.49706 | 0.0382258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136006 | TGTTCACTTTCCTGA[C/G]CAGAATTAAGCTCTT | 221178 |
rs4770603 | snp | G/T | 0.242201 | 0.249878 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139535 | TACCATCTGTTATAT[G/T]AAGGTGCTGCAGAAA | 221178 |
rs4770604 | snp | A/G | 0.417034 | 0.18601 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139954 | GCACCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG | 221178 |
rs4770606 | snp | C/T | 0.465158 | 0.127307 | intron-variant | SPATA13 | GRCh38.p7 | 13:24151657 | CTCAACTGTCCAAGT[C/T]CAAACACCAGCTGTG | 221178 |
rs4770611 | snp | C/T | 0.491263 | 0.0655142 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24160344 | TCCGCCTCTCGGGTT[C/T]AAGTGATTCTCCTGC | 221178 |
rs4770612 | snp | C/T | 0.241053 | 0.24984 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163185 | GAGGATTGCTTGAGC[C/T]CAGGAGTTCAAGACC | 221178 |
rs4770613 | snp | C/T | 0.490231 | 0.0692021 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163284 | GCACTCACCTGTAGT[C/T]CAAGGTGCTCAGGAG | 221178 |
rs4770614 | snp | A/C | 0.24134 | 0.24985 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163286 | ACTCACCTGTAGTCC[A/C]AGGTGCTCAGGAGGC | 221178 |
rs4770617 | snp | G/T | 0.454061 | 0.144427 | intron-variant | SPATA13 | GRCh38.p7 | 13:24188499 | aaagtctaatccaaa[G/T]caagtctctaactct | 221178 |
rs4770619 | snp | C/T | 0.453939 | 0.144598 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189082 | aatggagaagtacaa[C/T]gagatgaatattgtt | 221178 |
rs4770620 | snp | C/T | 0.441295 | 0.160954 | intron-variant | SPATA13 | GRCh38.p7 | 13:24190737 | agtggtttcttgtga[C/T]ggaaactacctctgg | 221178 |
rs4770623 | snp | A/G | 0.488846 | 0.0738428 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194608 | TAATAGCTGCATAAT[A/G]AGCCCGGTAGGTCCT | 221178 |
rs4770625 | snp | C/T | 0.159622 | 0.233092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206015 | ttcagggcataggaa[C/T]gagcaaagatttcat | 221178 |
rs4770626 | snp | A/G | 0.385932 | 0.209815 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207541 | ctatttcacatttcc[A/G]ccaacagtacacccg | 221178 |
rs4770627 | snp | C/T | 0.380529 | 0.213219 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207873 | ggtggccctgtcact[C/T]tctatggtgtgatct | 221178 |
rs4770628 | snp | A/G | 0.372391 | 0.217992 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207926 | GCATCTGTGAAATGG[A/G]TGTGATAATAGAGGG | 221178 |
rs4770629 | snp | A/G | 0.383824 | 0.211166 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207965 | TTGAGAATATCTGGC[A/G]TATAGACATTCTCTC | 221178 |
rs4770633 | snp | A/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232537 | tggcttgtcttttaa[A/T]ttttttaatattttt | 221178 |
rs4770639 | snp | A/G | 0.440057 | 0.162414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261601 | GGACCAGTGAAGGCA[A/G]AGAAATTCACAAAGA | 221178 |
rs4770640 | snp | A/G | 0.279195 | 0.248289 | intron-variant | SPATA13 | GRCh38.p7 | 13:24271412 | GGTTTAAGGCTGTGA[A/G]CTGATCTTTGAAAAA | 221178 |
rs4770641 | snp | C/T | 0.293037 | 0.246268 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272710 | GGCTCATAGCAGGAT[C/T]GCTTTGCTGGCAGAC | 221178 |
rs4770642 | snp | A/G | 0.214843 | 0.247516 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279613 | ctttcaggaacttga[A/G]tcagatctgccagtg | 221178 |
rs5016965 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291756 | TTTTTTTATTTTTTT[A/T]TTTTTTTTTTTGAGA | 221178 |
rs5021764 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024618 | GATCCCGCTATGATG[C/T]ATCCAGTGCTTACTA | 221178 |
rs5021765 | snp | A/C | 0.49975 | 0.0111793 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024595 | AGAGCAGCTGGCACG[A/C]TGCTGCTGATCCCGC | 221178 |
rs5802259 | in-del | -/CTT | 0.271702 | 0.249056 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011899 | CCCAGAATGCTCAGC[-/CTT]CTTCTTTAAACTTGC | 221178 |
rs5802261 | in-del | -/A | 0.499653 | 0.0131743 | intron-variant | SPATA13 | GRCh38.p7 | 13:24024685 | AATATTTGATGACAT[-/A]AAAATGTTATATATT | 221178 |
rs5802262 | in-del | -/A | 0.496778 | 0.0400063 | intron-variant | SPATA13 | GRCh38.p7 | 13:24048681 | TCTCTGATCAAAATT[-/A]AAAAAAAAGATAAAT | 221178 |
rs5802263 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24100143 | ATTTTTAAATAGTTT[-/A]AAAAAAAAAAAGAAT | 221178 |
rs5802264 | in-del | -/T | 0.0592699 | 0.161623 | intron-variant | SPATA13 | GRCh38.p7 | 13:24134574 | ATTGGTTTGTTTTTT[-/T]AGCACGGGGAGTAGC | 221178 |
rs5802265 | in-del | -/C | 0 | 0 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159111 | AGATAATAAAAAAAC[-/C]CCTCAATTTAGACCG | 221178 |
rs5802266 | in-del | -/G/T | 0.916766 | 0.130711 | upstream-variant-2KB, intron-variant | SPATA13 | GRCh38.p7 | 13:24159131 | ATTTAGACCGTGATA[-/G/T]TTTTTTTTTAAATAA | 221178 |
rs5802267 | in-del | -/T/TT | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24198966 | TTTTTTTTTTTTTTT[-/T/TT]AAGGCAGGGTCTTAC | 221178 |
rs5802269 | in-del | -/GTGGGGG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24208580 | AGAAGACTGGTGGGG[-/GTGGGGG]ACTTTCCAGACTGAT | 221178 |
rs5802270 | in-del | -/G | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208704 | GCCCATAGGCCAAAA[-/G]AAATCCCTGACAGTT | 221178 |
rs5802271 | in-del | -/G | 0.377582 | 0.214995 | intron-variant | SPATA13 | GRCh38.p7 | 13:24221479 | GATGGGAAAGGTTAA[-/G]GGGGAGCAGGATTTT | 221178 |
rs5802273 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SPATA13, SPATA13-AS1 | GRCh38.p7 | 13:24254818 | CTTCTTTTTTTTTTT[-/T]CCTTTTTATGAACCC | 221178 |
rs5802276 | snp | A/T | 0.375 | 0.216506 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291748 | TGTCTTTATTTTTTT[A/T]TTTTTTTATTTTTTT | 221178 |
rs5802277 | in-del | -/A | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24291753 | TATTTTTTTATTTTT[-/A]TTATTTTTTTTTTTG | 221178 |
rs6144956 | in-del | -/GGTAAGAGGAATCCTTG | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24288563 | CTGGTGGAATCCTTG[-/GGTAAGAGGAATCCTTG]CCCTGATGAACAGTG | 221178 |
rs6416353 | snp | C/G | 0.226484 | 0.248892 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065554 | CAGCGTGGCATATAT[C/G]AATATTAGCAAGTAA | 221178 |
rs6490851 | snp | C/T | 0.397633 | 0.201754 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983130 | GAGAGTGTCTTTGTT[C/T]GGGCTGCCATCACAA | 221178 |
rs6490853 | snp | G/T | 0.471578 | 0.115772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003971 | TTTTGTACACTTGCT[G/T]CATATACATACACAC | 221178 |
rs6490854 | snp | C/T | 0.222928 | 0.24853 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041397 | CAGAGTAGCATAATC[C/T]ATGATGCCTATGTCC | 221178 |
rs6490855 | snp | C/T | 0.152667 | 0.230274 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041488 | GATATCGTCATATAA[C/T]AGATAAAGCTAAACA | 221178 |
rs6490856 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041609 | CATGGTGATGTTAAG[A/G]AAATGTTTTCTTTTC | 221178 |
rs6490857 | snp | C/T | 0.494526 | 0.0520291 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045014 | CTTCCTTTATTCTTT[C/T]GTGTTTCCCTTGAAC | 221178 |
rs6490858 | snp | G/T | 0.4944 | 0.0526182 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045060 | AAAATCCAGGGCGGC[G/T]GAGTTTGTAAGATTT | 221178 |
rs6490859 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045210 | TGTCTTCTTTGAATA[A/G]CTGATCTATTTCCTT | 221178 |
rs6490860 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045288 | CTAAATTTAATATTC[A/G]ACCATGACCTTTGTA | 221178 |
rs6490861 | snp | A/T | 0.494976 | 0.0498674 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045295 | TAATATTCGACCATG[A/T]CCTTTGTATTATGTT | 221178 |
rs6490862 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045318 | ATTATGTTTCTTCCC[C/T]TTCTATGAGGTTTTA | 221178 |
rs6490863 | snp | C/T | 0.489608 | 0.0713316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24050105 | TCGAACTCCTGACCT[C/T]GTGATCCACCCACCT | 221178 |
rs6490865 | snp | A/G | 0.225005 | 0.248747 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065592 | TTGGATAACAAAAAT[A/G]TAAGCTCCTCACAAG | 221178 |
rs6490866 | snp | C/T | 0.191775 | 0.243125 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070343 | TCTCCTTGCCTCCTC[C/T]GCCGCCCCCCTACCA | 221178 |
rs6490867 | snp | A/G | 0.207253 | 0.246318 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082164 | AGTTGCTTGACATGC[A/G]GGATCCAAAATACAT | 221178 |
rs6490868 | snp | A/C | 0.210301 | 0.246828 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092038 | agtcatagtctttga[A/C]taaacactttactcc | 221178 |
rs6490869 | snp | G/T | 0.254664 | 0.249956 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095328 | caaaaggacaagtac[G/T]gtatgattccactta | 221178 |
rs6490870 | snp | A/G | 0.499424 | 0.0169631 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095569 | atggttatgatggta[A/G]atatgtatattttgc | 221178 |
rs6490871 | snp | A/T | 0.242488 | 0.249887 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095676 | TCTACAGACTTCTCT[A/T]CTATGTGGATGCAAA | 221178 |
rs6490872 | snp | C/T | 0.498964 | 0.02274 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139201 | cacacagctttttcc[C/T]atgtgtctctgagtc | 221178 |
rs6490873 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24139466 | TTCTCCTCTGGGATT[C/G]TATCACTGGCAGGTG | 221178 |
rs6490874 | snp | A/T | 0.449091 | 0.151204 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142473 | CCCCCTCAGTTTTGG[A/T]TTGTCTGATGTTTTC | 221178 |
rs6490875 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144611 | TCTTTGGTGCCTGCA[A/G]GTTGCTGCCATTGTG | 221178 |
rs6490876 | snp | C/T | 0.464416 | 0.128553 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153213 | GAGCTGTCATGCTGG[C/T]CTGTCTCATGTATGT | 221178 |
rs6490877 | snp | C/T | 0.476227 | 0.106402 | intron-variant | SPATA13 | GRCh38.p7 | 13:24168542 | TAAGCAAAACTCTAC[C/T]GCTGGGGAAACTTTT | 221178 |
rs6490884 | snp | C/T | 0.203267 | 0.245593 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200387 | CTGTTTTATTAAATA[C/T]TTAATTCATACAAAG | 221178 |
rs6490885 | snp | A/G | 0.26518 | 0.249539 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200561 | TCGGGGATTATCACC[A/G]CTTAACTCTTCTTTA | 221178 |
rs6490886 | snp | A/T | 0.482757 | 0.0912364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215727 | CTGCACTGTTGGGTG[A/T]CTTAGCCTGTGAACT | 221178 |
rs6490887 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | SPATA13 | GRCh38.p7 | 13:24219678 | GAGATGCCTGAAGGC[C/T]TGTGGAAGCACAGAG | 221178 |
rs6490889 | snp | A/G | 0.429837 | 0.173662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24262192 | TTTGATTTTTTAAAT[A/G]AAATTAATTGAATTA | 221178 |
rs6490891 | snp | C/T | 0.496649 | 0.0407971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301593 | ACGTTCACAGGTGGC[C/T]ACCGGGTGGGACGCT | 221178 |
rs6490892 | snp | G/T | 0.0267878 | 0.112589 | utr-variant-3-prime | SPATA13 | GRCh38.p7 | 13:24304941 | AATACAATGATATAT[G/T]TTGGAAACTACTTAA | 221178 |
rs6650255 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101210 | TTCTTATCCTCTCTT[C/G]TCTTTCTCGCCACAC | 221178 |
rs6650256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101283 | ATACCATTTCATCAT[A/G]CAGATGCACCATGAA | 221178 |
rs7139472 | snp | C/T | 0.425277 | 0.178263 | intron-variant | SPATA13 | GRCh38.p7 | 13:24268631 | GGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 221178 |
rs7139478 | snp | C/G | 0.389782 | 0.256681 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189243 | TTGGGAGGCCGAGGC[C/G]GGTGGATCACGACGT | 221178 |
rs7139760 | snp | C/G | 0.234401 | 0.249513 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198499 | TTAAATCCTTCAGAC[C/G]CAGTTAATAAAATCC | 221178 |
rs7139885 | snp | C/G | 0.499 | 0.0223418 | intron-variant | SPATA13 | GRCh38.p7 | 13:24006532 | TCAGGGCACGAGGTG[C/G]GGCAGAGGAGCGAAT | 221178 |
rs7140029 | snp | A/C | 0.181978 | 0.240568 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189483 | CATCTCTCTCTCTCT[A/C]TATATATATACGTGT | 221178 |
rs7140061 | snp | C/T | 0.462582 | 0.131564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152872 | CTCTCCTCCCTCAAA[C/T]GTTCAGAACTCAAAT | 221178 |
rs7316990 | snp | C/T | 0.225005 | 0.248747 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065154 | CCTGTCAGGGGGATG[C/T]CTAATAATGCACATG | 221178 |
rs7317009 | snp | A/G | 0.493703 | 0.0557558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131474 | GAATCCTCCAAGGGC[A/G]TGGAAATCACTAGAA | 221178 |
rs7317180 | snp | C/T | 0.34526 | 0.23114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198140 | AGCTGGGATTACAGG[C/T]GCCCGCCACCATGCC | 221178 |
rs7317204 | snp | A/G | 0.493703 | 0.0557558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131566 | GGATGCTGAAATGTC[A/G]AGATTTACAAGACAT | 221178 |
rs7317248 | snp | C/T | 0.126564 | 0.217402 | intron-variant | SPATA13 | GRCh38.p7 | 13:24153081 | TCTACTTAGGACCTC[C/T]GAGTTGGGACTTGGG | 221178 |
rs7318162 | snp | C/G | 0.349013 | 0.229557 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198642 | TTGGAATTTAAAACT[C/G]TATGTATGTTCAAGC | 221178 |
rs7318203 | snp | C/T | 0.451483 | 0.148002 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222228 | CTGGCATGTCCTTGC[C/T]GAGTCCTTCCCGCCT | 221178 |
rs7318364 | snp | C/T | 0.250168 | 0.25 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198754 | TCCCACGTGCTGCCA[C/T]GAGGACATGGAAACT | 221178 |
rs7318560 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106929 | AGGTAGCCATGTAGT[A/G]AAGTCTGTGCACTAT | 221178 |
rs7318566 | snp | C/G | 0.488545 | 0.074807 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251284 | ATGAGGCTGAAGAAG[C/G]ATGTGAGGATCACAG | 221178 |
rs7318607 | snp | A/G | 0.39214 | 0.205661 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202058 | agcctgggggacaga[A/G]caagactctgtctaa | 221178 |
rs7318680 | snp | A/G | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24031288 | ACCAAGGTCTGGTCC[A/G]TAGCATAACTGGTTG | 221178 |
rs7318885 | snp | C/G | 0.246769 | 0.249979 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040175 | ACCAAATGGCGAGTG[C/G]CCTATGCCAGCAAAA | 221178 |
rs7318898 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200948 | TGATTACGTCCTTGT[A/T]CTTTTTTTTCCCCCT | 221178 |
rs7318909 | snp | A/G | 0.494609 | 0.0516363 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107067 | CGGGGAAAAAAAAAA[A/G]GAAGAAATTTATGCT | 221178 |
rs7318988 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068585 | gttgaactaatttac[A/G]ctttcactgacagtg | 221178 |
rs7319037 | snp | A/G | 0.251014 | 0.249998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198761 | TGCTGCCACGAGGAC[A/G]TGGAAACTAGTAAAG | 221178 |
rs7319130 | snp | C/G | 0.498206 | 0.0298983 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137296 | TCCAGCCCTGGGTTT[C/G]CCAGGggcctgctcc | 221178 |
rs7319154 | snp | A/G | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24251590 | TGCAGCCTGCAACTC[A/G]TGGCAGGATTGGAGA | 221178 |
rs7320152 | snp | A/T | 0.450105 | 0.149859 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089816 | CTTGTGGTTCTCGAG[A/T]TTGGAAGTCCAAGAT | 221178 |
rs7320360 | snp | C/T | 0.491577 | 0.0643472 | intron-variant | SPATA13 | GRCh38.p7 | 13:24068610 | acagtgtataagcat[C/T]cctttttctccacaa | 221178 |
rs7320607 | snp | A/G | 0.316485 | 0.240998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211499 | gctttttctgtatct[A/G]ttgagatagtcctat | 221178 |
rs7320781 | snp | A/G | 0.316243 | 0.241064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211567 | tttagtaaatattgt[A/G]tatttatttaGTAAG | 221178 |
rs7320787 | snp | A/G | 0.109461 | 0.206758 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102103 | attcccactaacagc[A/G]cgtagggttccaatt | 221178 |
rs7320827 | snp | A/G | 0.316243 | 0.241064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211643 | CTCCCCTCTCTCCAT[A/G]TTGTCCAGCTGGTCA | 221178 |
rs7320910 | snp | C/T | 0.112983 | 0.209108 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232620 | aatcacagcttactg[C/T]agcctcaacctccca | 221178 |
rs7321078 | snp | A/C | 0.112631 | 0.208878 | intron-variant | SPATA13 | GRCh38.p7 | 13:24232670 | cctcagcaccacccc[A/C]acccagtagctggga | 221178 |
rs7321200 | snp | A/G | 0.356597 | 0.226135 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019380 | GGCGTGAGCCACCAC[A/G]CCCGGCCATGATTCT | 221178 |
rs7321356 | snp | A/G | 0.34437 | 0.231505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037439 | ttgagatagagtctc[A/G]ctctgttgcccaggc | 221178 |
rs7321406 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107662 | CAATGACAGCGCCTA[C/T]GTCAGCTTTTCTTCC | 221178 |
rs7321923 | snp | C/G | 0.364817 | 0.222075 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111139 | GGTCTTGAACCCCTG[C/G]TTTCAAGTGATCCTC | 221178 |
rs7321973 | snp | A/C | 0.316485 | 0.240998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211465 | ttttatcatgaaaga[A/C]tgttgaattttgtca | 221178 |
rs7322015 | snp | G/T | 0.409608 | 0.192419 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199019 | agtggttcattcttt[G/T]ttctcttttcaggca | 221178 |
rs7322143 | snp | C/T | 0.465996 | 0.12588 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102071 | atattttttccatag[C/T]agctgcaccatttta | 221178 |
rs7322284 | snp | A/G | 0.316243 | 0.241064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211322 | agagtggacatcctt[A/G]tcttatttctgatgc | 221178 |
rs7322332 | snp | A/G | 0.162253 | 0.234095 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23977751 | AATTTCTGTCTTTCA[A/G]AGAATCTTTTTTATC | 221178 |
rs7322365 | snp | G/T | 0.347914 | 0.230028 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199167 | gttctgggattacag[G/T]cctgagccactgcgc | 221178 |
rs7322383 | snp | C/T | 0.314544 | 0.241524 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211729 | TCTCATCCGGTGGCA[C/T]TGACGATGATGGCCT | 221178 |
rs7322473 | snp | C/G | 0.400682 | 0.199487 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111411 | TCTCTGTCCTGCCCC[C/G]CCACCCCCACCCCAg | 221178 |
rs7322486 | snp | A/T | 0.316485 | 0.240998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211430 | gaagaacattcctgt[A/T]tgccatatttgttga | 221178 |
rs7322682 | snp | A/T | 0.4661 | 0.125701 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101853 | ttctgttgtgtgtgt[A/T]taccacatgttcttt | 221178 |
rs7323080 | snp | A/G | 0.314544 | 0.241524 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211735 | CCGGTGGCACTGACG[A/G]TGATGGCCTCTGCTG | 221178 |
rs7323092 | snp | C/T | 0.315516 | 0.241263 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118916 | cttttcttttctttt[C/T]tttttttgagatgga | 221178 |
rs7323478 | snp | A/G | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208229 | TCCCAGAATAGTGAC[A/G]GAACTGGGGAGTGAT | 221178 |
rs7323612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111261 | AGTGAAAAAAAAATT[C/G]TAACAAACTATAATA | 221178 |
rs7323622 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132594 | AAAAGTATTAACATT[A/G]TTAGGAAGGTAAAGA | 221178 |
rs7323711 | snp | A/G | 0.133435 | 0.221162 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208356 | TGGTTCCAATTCCAA[A/G]TTGCACCACTGTGGA | 221178 |
rs7323812 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SPATA13 | GRCh38.p7 | 13:24072487 | CCATCCTGTTCTATC[A/G]GGGCTTCTGATGCAC | 221178 |
rs7323841 | snp | C/T | 0.40086 | 0.199352 | intron-variant | SPATA13 | GRCh38.p7 | 13:24111409 | CCTCTCTGTCCTGCC[C/T]CGCCACCCCCACCCC | 221178 |
rs7323845 | snp | G/T | 0.128976 | 0.218754 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198675 | GGAGGTGAGTTTTGT[G/T]TGGTAGTCTCTTTTT | 221178 |
rs7323877 | snp | C/T | 0.227369 | 0.248974 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039957 | GAGGGCCTTTCTGAG[C/T]GGTGGAGCCCAAGCT | 221178 |
rs7323885 | snp | A/G | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208422 | TTGAAGTGAAACAGT[A/G]TAATTCATAATCCCC | 221178 |
rs7324255 | snp | C/T | 0.470811 | 0.117228 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237973 | acatgtttaaatatg[C/T]aatatataaacatgt | 221178 |
rs7324314 | snp | A/G | 0.108402 | 0.206034 | intron-variant | SPATA13 | GRCh38.p7 | 13:24090663 | CCCCAACttactgat[A/G]ttccctatttgataa | 221178 |
rs7324542 | snp | A/G | 0.0577266 | 0.159784 | missense, intron-variant | SPATA13 | GRCh38.p7 | 13:24224427 | TCCGCGAATTCAGAG[A/G]AAAGTGAAGGAAGGG | 221178 |
rs7324841 | snp | A/T | 0.339882 | 0.233284 | intron-variant | SPATA13 | GRCh38.p7 | 13:24120002 | GCCATCCCCAGCCCC[A/T]CCCCCACAGAGTGAC | 221178 |
rs7325215 | snp | C/G | 0.386123 | 0.209692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178271 | GCCACTGCTTGCCAC[C/G]TCTGCCACCTGTGAG | 221178 |
rs7325299 | snp | C/T | 0.359787 | 0.224604 | intron-variant | SPATA13 | GRCh38.p7 | 13:24011067 | GCACTCTGCAGTTTG[C/T]TGACTCCTCTGCAAC | 221178 |
rs7325329 | snp | C/G | 0.397813 | 0.201621 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981732 | AGCCTCATGTCTCAC[C/G]GCCAGTCAGGCTCAA | 221178 |
rs7325589 | snp | A/G | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208259 | TCAGCTTTCTTCCAG[A/G]AATTCCCTGTAATTG | 221178 |
rs7325698 | snp | C/T | 0.484561 | 0.0864924 | intron-variant | SPATA13 | GRCh38.p7 | 13:24178556 | TGAGCTTACTCTGTG[C/T]CATGCATTGCTAGGA | 221178 |
rs7325740 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24019167 | GATCTCGGCTCACTG[C/T]AAGCTCCGCCTCCCG | 221178 |
rs7325917 | snp | C/G | 0.316726 | 0.240931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211884 | TGCACCCCAACATCC[C/G]TCCTTTCTCTGGCAT | 221178 |
rs7325920 | snp | C/T | 0.492533 | 0.0606443 | intron-variant | SPATA13 | GRCh38.p7 | 13:24137256 | GGGGTGAAAGGCCAC[C/T]GAACTGAAAGAAGAA | 221178 |
rs7326088 | snp | C/T | 0.383824 | 0.211166 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208825 | TTCTTCAGAAATTAC[C/T]GCACTTGGTTTAATT | 221178 |
rs7326148 | snp | A/G | 0.379942 | 0.213577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129080 | TTGAATTCCTCTGAT[A/G]GGCTGACTTCTAATG | 221178 |
rs7326164 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129112 | TCCTATACTTTAAAG[A/G]AGTGGCTTCTGCAGC | 221178 |
rs7326287 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041351 | CTCTCTTTCAAGCTC[A/G]TTTTCCCTATTGACA | 221178 |
rs7326323 | snp | G/T | 0.350327 | 0.228986 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086956 | CGGTCTCTAATCTGG[G/T]CTAAGAAGTGAATCT | 221178 |
rs7326642 | snp | C/G | 0.136166 | 0.22258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045015 | TTCCTTTATTCTTTC[C/G]TGTTTCCCTTGAACT | 221178 |
rs7326788 | snp | C/T | 0.142609 | 0.225759 | intron-variant | SPATA13 | GRCh38.p7 | 13:24224857 | TTTATTGAACATGTA[C/T]CAGGTACTAGATTCT | 221178 |
rs7326876 | snp | C/T | 0.316 | 0.241131 | intron-variant | SPATA13 | GRCh38.p7 | 13:23990181 | TTCCCTCAGCCACCT[C/T]CAGCTGTGTTGTTGC | 221178 |
rs7326946 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | SPATA13 | GRCh38.p7 | 13:24202690 | ACAGACGGAAGAGAG[C/T]GAGAACTGTCTTATT | 221178 |
rs7327051 | snp | C/T | 0.122064 | 0.214785 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203302 | TGTCAGGGTAATCAC[C/T]AATTACCCTGACGGT | 221178 |
rs7327245 | snp | A/G | 0.393987 | 0.204372 | intron-variant | SPATA13 | GRCh38.p7 | 13:24225925 | ccacatccaggaaaa[A/G]tgaagttacgtggac | 221178 |
rs7327336 | snp | C/T | 0.316726 | 0.240931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211909 | TGGCATTAGAGCATC[C/T]GTGTGTCGGCTGAAG | 221178 |
rs7327407 | snp | A/G | 0.268995 | 0.249277 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094748 | tgcactccagcctgg[A/G]caatatagcaagacc | 221178 |
rs7327593 | snp | C/G | 0.260227 | 0.249791 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064058 | TCAAGTCAGCCATTT[C/G]TCTCTTTGACCATGC | 221178 |
rs7327669 | snp | C/T | 0.355311 | 0.226737 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226504 | TCATATTCTATCAAA[C/T]ATCTTTATAATTTTC | 221178 |
rs7327723 | snp | C/T | 0.177182 | 0.23916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203663 | GGGGCTTAAATTTCA[C/T]GGGTTCTTCAATTCT | 221178 |
rs7327740 | snp | C/T | 0.316243 | 0.241064 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211566 | ATTTAGTAAATATTG[C/T]GTATTTATTTAGTAA | 221178 |
rs7327883 | snp | C/T | 0.316 | 0.241131 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212247 | TGGGCCACTCCAGCC[C/T]GCACCAGGCTGCACT | 221178 |
rs7327973 | snp | C/T | 0.314057 | 0.241654 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211716 | ACGGCCAGGATTATC[C/T]CATCCGGTGGCACTG | 221178 |
rs7327979 | snp | A/G | 0.316726 | 0.240931 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211931 | CGGCTGAAGGAGGCC[A/G]CTTCAGGCTTCATAA | 221178 |
rs7328758 | snp | C/T | 0.495782 | 0.0457324 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132757 | GGCAGGTGGATCACC[C/T]GAGGTCAAGAGTTCG | 221178 |
rs7328904 | snp | C/T | 0.497387 | 0.0360476 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064720 | tatggtactttgtta[C/T]agcagccaaactaaa | 221178 |
rs7328909 | snp | A/G | 0.152667 | 0.230274 | intron-variant | SPATA13 | GRCh38.p7 | 13:24087236 | CAGGGGTGAGGCCCC[A/G]AGACAAGGGGCCTGG | 221178 |
rs7328922 | snp | A/G | 0.184203 | 0.241186 | intron-variant | SPATA13 | GRCh38.p7 | 13:24037951 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGCATTGC | 221178 |
rs7329133 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SPATA13 | GRCh38.p7 | 13:24082406 | TCTGTGGCGGGGAGG[A/G]TAACACTGATGGAGA | 221178 |
rs7329319 | snp | C/G | 0.31014 | 0.242659 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052383 | CATCGCTACAAACAA[C/G]AACAACAACAACAAA | 221178 |
rs7329726 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237883 | tataatatatatcat[A/T]tataatatataaaca | 221178 |
rs7329958 | snp | C/T | 0.371987 | 0.218218 | intron-variant | SPATA13 | GRCh38.p7 | 13:24207942 | TGTGATAATAGAGGG[C/T]AGTTGTGTTGAGAAT | 221178 |
rs7329991 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | SPATA13 | GRCh38.p7 | 13:24052739 | GAATATAAATATTCA[A/G]CATCCTGGCCTTGGA | 221178 |
rs7330416 | snp | A/T | 0.267908 | 0.249358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24199707 | ttgtttgcctagacc[A/T]gcggcaatgtattgg | 221178 |
rs7330484 | snp | G/T | 0.294576 | 0.245994 | intron-variant | SPATA13 | GRCh38.p7 | 13:24215460 | GGACATCCCCTACCT[G/T]AAGACCTGATAGGCT | 221178 |
rs7330736 | snp | C/T | 0.0646939 | 0.167814 | missense | SPATA13 | GRCh38.p7 | 13:24249756 | TGCCCCAAAGGAGCC[C/T]GGAGAAGGCGCCCCA | 221178 |
rs7330756 | snp | C/T | 0.330714 | 0.236612 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980872 | GCTGGGATTAGAAGC[C/T]TGAGCCACTGCGCCT | 221178 |
rs7330926 | snp | C/G | 0.0788843 | 0.182262 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295580 | tcgtgcccctgcact[C/G]tagtctgggtgacag | 221178 |
rs7330947 | snp | C/T | 0.342582 | 0.232225 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033261 | CTAATAAAAATGAAA[C/T]GAAAGCAGTCAAGTA | 221178 |
rs7331042 | snp | C/T | 0.473081 | 0.112848 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209049 | GTCAGCTGTGGCTTC[C/T]TGGTTCCTGCCACTG | 221178 |
rs7331045 | snp | C/G | 0.31503 | 0.241394 | intron-variant | SPATA13 | GRCh38.p7 | 13:24026798 | tagccaggatggtct[C/G]gatctcctgacctcg | 221178 |
rs7331492 | snp | C/T | 0.380333 | 0.213338 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129263 | CCAACCATCAAAGTC[C/T]GAGTACAGCGTCTGT | 221178 |
rs7331517 | snp | G/T | 0.350546 | 0.22889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24129291 | TGTCCCATGTGAGCA[G/T]GAGGGAAAGGGAATC | 221178 |
rs7331859 | snp | G/T | 0.49783 | 0.0586125 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041631 | TTTCTTTTCATTCTT[G/T]TTCTTCTTAGTGGGA | 221178 |
rs7331947 | snp | A/C | 0.472709 | 0.11358 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209068 | TTCCTGCCACTGTTG[A/C]TGAGCTCTCAGCACT | 221178 |
rs7332020 | snp | A/G | 0.49925 | 0.0193545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24061091 | acttttcaaaagagg[A/G]catacatgtggctaa | 221178 |
rs7332038 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SPATA13 | GRCh38.p7 | 13:23991224 | CTTCAAGGGCAGCCC[G/T]TCTAAGAACCTGTGC | 221178 |
rs7332336 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | SPATA13 | GRCh38.p7 | 13:24246458 | CCTGTGAATTTTAAG[A/G]CCTGTGAATTAAATT | 221178 |
rs7332807 | snp | A/C | 0.455858 | 0.141853 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149351 | TCTCTTTATGTTCTC[A/C]TATGTGAGATCGTGG | 221178 |
rs7333022 | snp | A/G | 0.495016 | 0.0496707 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209645 | gtgtgtatacaccac[A/G]ttttctttatccatt | 221178 |
rs7333036 | snp | A/G | 0.48498 | 0.0853497 | intron-variant | SPATA13 | GRCh38.p7 | 13:24209658 | acattttctttatcc[A/G]ttcatccattcaggg | 221178 |
rs7333320 | snp | C/T | 0.48178 | 0.0936921 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165650 | TGTCTGGGACAGATG[C/T]ACGGGGAGGGCAGGC | 221178 |
rs7333383 | snp | A/G | 0.440746 | 0.161604 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065282 | AAACTTCCCCCATGT[A/G]CTGAGCTTCAGAGTG | 221178 |
rs7333431 | snp | A/G | 0.495095 | 0.0492773 | intron-variant | SPATA13 | GRCh38.p7 | 13:24145958 | CGACCAAGTCAACAG[A/G]CATAGACTGCGGGGG | 221178 |
rs7333520 | snp | A/T | 0.203575 | 0.245652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24064127 | CTGCACCTGTTCTCC[A/T]GCCTCATCAGGCCAC | 221178 |
rs7333647 | snp | C/T | 0.445592 | 0.155704 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212218 | AGGAGTTCAGGGCTG[C/T]GGGGAGCTGTGATTG | 221178 |
rs7333705 | snp | C/T | 0.486855 | 0.0799975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24165807 | ACTTGAGTGTTAATG[C/T]GACAATTCAGTCTCA | 221178 |
rs7333742 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183418 | AGTACACAAAATAGC[A/G]TTGTGTTTAAGGGTT | 221178 |
rs7333781 | snp | A/G | 0.49645 | 0.0419827 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070413 | GAAAGGAAGAGAGAG[A/G]GGAGATATCTCTTTC | 221178 |
rs7333976 | snp | C/T | 0.349233 | 0.229462 | intron-variant | SPATA13 | GRCh38.p7 | 13:24029968 | tctaattctttttta[C/T]ggctgcatagtattc | 221178 |
rs7334243 | snp | C/G | 0.239326 | 0.249772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065036 | catcctggatgggac[C/G]ttgCGTTTATATTAA | 221178 |
rs7334415 | snp | C/T | 0.224709 | 0.248717 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065080 | TACAACATTTATAGT[C/T]TCAATGTCAGAAACT | 221178 |
rs7334441 | snp | A/G | 0.46855 | 0.121392 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146407 | AGTACCCTTGTGATC[A/G]TTAGCTGCTTCCATG | 221178 |
rs7334520 | snp | A/G | 0.450105 | 0.149859 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222360 | CATGCTTATTCCTGC[A/G]TGTGCCAGCACTTGG | 221178 |
rs7334772 | snp | A/T | 0.23846 | 0.249734 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094859 | TAAGTAAAAACCTCC[A/T]taccaccttataccc | 221178 |
rs7334897 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | SPATA13 | GRCh38.p7 | 13:24030068 | cacacacacacacgc[A/G]cacacacacacacac | 221178 |
rs7334898 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24030070 | cacacacacacgcac[A/G]cacacacacacacac | 221178 |
rs7334958 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995128 | gtcagtagtgccaag[G/T]ttcgggaaccctgAC | 221178 |
rs7335101 | snp | A/G | 0.418974 | 0.184249 | intron-variant | SPATA13 | GRCh38.p7 | 13:24222602 | TTTACCTTCATGTCC[A/G]TGGCACAGCCCATAA | 221178 |
rs7335477 | snp | A/G | 0.323671 | 0.238899 | intron-variant | SPATA13 | GRCh38.p7 | 13:24133867 | GAGCGAGTCCCCAGG[A/G]TGTGGCCTCCAGAAG | 221178 |
rs7335680 | snp | C/G | 0.46845 | 0.121572 | intron-variant | SPATA13 | GRCh38.p7 | 13:24146301 | ACTGACAAGGCTGTT[C/G]CCATTGTGAAAGGGA | 221178 |
rs7336084 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301431 | ATCTTTAAGGCAGAA[A/G]AACCCATGTTATTAA | 221178 |
rs7336612 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142681 | tcatccttcttcctc[G/T]tcctcttcctcttcc | 221178 |
rs7336618 | snp | A/C | 0.483563 | 0.0891524 | intron-variant, upstream-variant-2KB | SPATA13, MIR2276 | GRCh38.p7 | 13:24162107 | CTGCCCTCCTCCCGC[A/C]CTTTAGAGTTTCATG | 221178 |
rs7336646 | snp | C/T | 0.384017 | 0.211044 | intron-variant | SPATA13 | GRCh38.p7 | 13:24208885 | ATACTGTATTCACTC[C/T]TATACTGAAGATCGG | 221178 |
rs7336684 | snp | A/G | 0.49934 | 0.0181589 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118818 | GAAGAACTAACTGTT[A/G]TTTGGCTAACCACAC | 221178 |
rs7336773 | snp | A/G | 0.493969 | 0.05458 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106671 | CCTGGTTCTGGGGCC[A/G]ACAGAGCTGGCTCTC | 221178 |
rs7337007 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | SPATA13 | GRCh38.p7 | 13:24033423 | TGAACTCTCCTTTTC[C/T]ATTAATGACTATGGG | 221178 |
rs7337087 | snp | C/T | 0.343254 | 0.231956 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033986 | GAGGAGACCCTTTAT[C/T]TGCATCGCAATTCTG | 221178 |
rs7337169 | snp | C/T | 0.495445 | 0.0475058 | intron-variant | SPATA13 | GRCh38.p7 | 13:24076089 | TCCCCACTTGTAAAA[C/T]AGAGAAAAGAGGACT | 221178 |
rs7337335 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | SPATA13 | GRCh38.p7 | 13:24266975 | gattttAAGACTTCT[C/T]TGAACTATGGTTTAG | 221178 |
rs7337393 | snp | C/T | 0.470034 | 0.11868 | intron-variant | SPATA13 | GRCh38.p7 | 13:24171272 | GCCTCATGTGTTCAG[C/T]GCTGTCATTTTTCAA | 221178 |
rs7337499 | snp | A/T | 0.36021 | 0.224397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24136128 | TTATTAACAGGAAAT[A/T]ATTCATCTGAGTTTC | 221178 |
rs7337678 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131261 | AGGAATTTCCATCAC[A/G]TATGGGCATATCTTG | 221178 |
rs7337736 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003874 | AACACAATATACATC[A/G]GCAAATACAGAACCC | 221178 |
rs7337824 | snp | C/T | 0.227369 | 0.248974 | intron-variant | SPATA13 | GRCh38.p7 | 13:24297896 | AAATACTTCTGAATG[C/T]ACTTACAAGACAGAC | 221178 |
rs7337840 | snp | C/T | 0.362523 | 0.223246 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012168 | GAAAGCCTGCAGAGG[C/T]ATCAGTCTCTTTCCT | 221178 |
rs7337891 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131403 | CAAAACCATCTACCC[A/G]AAGCATCTCTACTTA | 221178 |
rs7338032 | snp | A/G | 0.468349 | 0.121752 | intron-variant | SPATA13 | GRCh38.p7 | 13:23995609 | TGGAATTTCATCTGT[A/G]TCTGATATGCATTTT | 221178 |
rs7338192 | snp | C/G | 0.452842 | 0.146134 | intron-variant | SPATA13 | GRCh38.p7 | 13:24189270 | acgtcaggagatgga[C/G]accatcctggctaac | 221178 |
rs7338464 | snp | A/G | 0.258288 | 0.249863 | intron-variant | SPATA13 | GRCh38.p7 | 13:24275013 | TATCACACCCTCACC[A/G]GGACTACCCTCCCCC | 221178 |
rs7338807 | snp | A/G | 0.120674 | 0.21395 | intron-variant | SPATA13 | GRCh38.p7 | 13:24263037 | ATCTAATGATTTTTC[A/G]TTGTATCACCCAGAG | 221178 |
rs7338824 | snp | A/T | 0.316485 | 0.240998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210177 | tcatctattatgggt[A/T]ttagtcctttacttg | 221178 |
rs7339148 | snp | A/G | 0.453575 | 0.145111 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198229 | TGAACTCCTGACCTT[A/G]TGATCTGCCCCCCTT | 221178 |
rs7339362 | snp | A/G | 0.331642 | 0.236293 | intron-variant | SPATA13 | GRCh38.p7 | 13:24198310 | CTTGTTTTGTTTCCA[A/G]ACTCACTGGACTAAA | 221178 |
rs7350652 | snp | A/C | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24013984 | CAAGTCTGGAGTGTG[A/C]TAGAGTCAGAGCCTC | 221178 |
rs7490420 | snp | C/T | 0.084364 | 0.187256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24040515 | GACACACAGATGGGG[C/T]TGGAGAGGAGGCTAC | 221178 |
rs7491802 | snp | A/G | 0.484209 | 0.0874434 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24034116 | AGGAATCATGAGACC[A/G]TCGACATTTAGCAGC | 221178 |
rs7981291 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24105033 | CTGCCTGCTTCCAGG[C/G]AGAAGAAGTCACTTG | 221178 |
rs7981327 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24118168 | AGCGTAGACCACCAC[C/T]GCAGAAGCCAGGTGC | 221178 |
rs7981441 | snp | A/G | 0.349671 | 0.229272 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075006 | ctgtttacacctgca[A/G]tttggttatgttttc | 221178 |
rs7981445 | snp | C/T | 0.369754 | 0.219451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277607 | GTTCCTATCCTGGTT[C/T]GGACCCAGCCCCTGT | 221178 |
rs7981510 | snp | A/C | 0.381113 | 0.21286 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277270 | taacatggtgaaacc[A/C]cgtctctactaaaaa | 221178 |
rs7981755 | snp | C/G | 0.376592 | 0.215579 | intron-variant | SPATA13 | GRCh38.p7 | 13:24272541 | GGGCAGGGGGCAGGG[C/G]AGGGGTTGTGGGGCT | 221178 |
rs7981846 | snp | A/G | 0.363568 | 0.222716 | intron-variant | SPATA13 | GRCh38.p7 | 13:24216043 | GCAGGGCAGTCTTCA[A/G]GGCTGAGGGCTGTGA | 221178 |
rs7982225 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | SPATA13 | GRCh38.p7 | 13:24301618 | GACGCTGTGCCTGGG[C/T]TATCTGATTTCTTCC | 221178 |
rs7982475 | snp | A/G | 0.369754 | 0.219451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277797 | GTCCTGTCCTTTAAG[A/G]TGGTAAGCGACCTAG | 221178 |
rs7982553 | snp | A/C | 0.181022 | 0.240296 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089313 | TTGCATGGGACCCCC[A/C]CACACACCACTCGGA | 221178 |
rs7982678 | snp | A/G | 0.466308 | 0.125343 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144267 | TCTCCCACATGCCTC[A/G]TGTACGTCACAAACA | 221178 |
rs7982745 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24080630 | CTTCCCCTTAAATTT[A/G]CAGGTAGATCTGAGA | 221178 |
rs7982870 | snp | G/T | 0.421051 | 0.182323 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074532 | atgcagcacttacta[G/T]gtatcaggcactgct | 221178 |
rs7982888 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104651 | AAGTATTAGGGGAAG[G/T]TCCCATCTTTGATGA | 221178 |
rs7982951 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | SPATA13 | GRCh38.p7 | 13:24156401 | AGACAGGGAGGCACC[A/G]TAGATGGCACACTGG | 221178 |
rs7983014 | snp | A/C | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24147278 | GAGATAGAATGATGA[A/C]CGTATTGAGTAACTG | 221178 |
rs7983191 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098794 | tagctgggcattttg[A/G]tgcgtgcatgtagtc | 221178 |
rs7983192 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098798 | tgggcattttggtgc[A/G]tgcatgtagtcctag | 221178 |
rs7983198 | snp | A/G | 0.163236 | 0.234461 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074883 | acaggaaagggaagt[A/G]aggcacagacacagc | 221178 |
rs7983208 | snp | A/G | 0.367708 | 0.220556 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074900 | ggcacagacacagct[A/G]ggctgggtgcagttt | 221178 |
rs7983228 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098857 | gcttgagcccaggag[G/T]tggaggttgcagtga | 221178 |
rs7983946 | snp | A/G | 0.244776 | 0.249945 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086015 | GATGAAGGAAACTCT[A/G]GGTTAGAGGACATCT | 221178 |
rs7984325 | snp | G/T | 0.137867 | 0.223442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092207 | CCAATGTTGATCTTT[G/T]AAAAGTGCTTTTGAG | 221178 |
rs7984381 | snp | A/G | 0.322007 | 0.239405 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241523 | CTTTGCATGGGTAAC[A/G]GGCTTTTATAGGAGC | 221178 |
rs7984482 | snp | G/T | 0.33303 | 0.235809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086287 | GTCTTGCTAAAAAAA[G/T]GGATCTGAAATTTAG | 221178 |
rs7984719 | snp | C/T | 0.137187 | 0.223099 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092432 | TTGGTATAACTGGAA[C/T]AAAAAGAGATAATGG | 221178 |
rs7984796 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24144400 | GAGACAAGATGAGCG[A/C]ATGAAACTAACATCA | 221178 |
rs7985197 | snp | C/T | 0.337386 | 0.23423 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055864 | AGTCCAATCCACCAC[C/T]GCACGGGTCCAGAAT | 221178 |
rs7985484 | snp | A/G | 0.489142 | 0.0728777 | intron-variant, downstream-variant-500B | SPATA13 | GRCh38.p7 | 13:24035344 | ATTTTTAATAGAGAC[A/G]GGTTTTGCCATGTGG | 221178 |
rs7985529 | snp | A/G | 0.338296 | 0.233889 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056776 | AGAAAAGACAAGTAC[A/G]TTGCTGTGCGTGTCT | 221178 |
rs7985555 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | SPATA13 | GRCh38.p7 | 13:24086197 | AAAATATAACAGGCC[C/T]GGCTACGTTTGAATT | 221178 |
rs7986211 | snp | C/T | 0.271432 | 0.24908 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277915 | GACACTGAGAAATCC[C/T]ACTCCATAAAACACA | 221178 |
rs7986503 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24056586 | aattgcctactgctg[C/T]acccacagagcccag | 221178 |
rs7986973 | snp | C/T | 0.19646 | 0.2442 | intron-variant | SPATA13 | GRCh38.p7 | 13:24278307 | GAGTTTCCTCATCTG[C/T]AAGTGGGGACAACTG | 221178 |
rs7987132 | snp | A/G | 0.362313 | 0.223351 | intron-variant | SPATA13 | GRCh38.p7 | 13:23984455 | CTCTGTAAGTTGAAT[A/G]GAAACCGTGTGCATT | 221178 |
rs7987799 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099045 | agctatgatcatacc[A/G]cttcactcctgccta | 221178 |
rs7987800 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074927 | gtttggcatttgcct[C/T]atttgaacagttggc | 221178 |
rs7987854 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24051027 | TGAGCTAAGCAGGCT[A/G]TAGACCCATATCTGC | 221178 |
rs7987967 | snp | G/T | 0.340108 | 0.233197 | intron-variant | SPATA13 | GRCh38.p7 | 13:24119476 | CTAGATGTTTTTCAG[G/T]GGGTCCAGACATGTA | 221178 |
rs7988546 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099458 | gtcgtcagtggccac[A/G]cacactagtggccgc | 221178 |
rs7988619 | snp | C/G | 0.155325 | 0.23138 | intron-variant | SPATA13 | GRCh38.p7 | 13:24107866 | TTAAGTCCTGTTATG[C/G]AAGATGCTCACTCGC | 221178 |
rs7988677 | snp | A/G | 0.384209 | 0.210922 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138043 | TAGTGGCTCGCGCAT[A/G]TAATCCCAGCAGTTT | 221178 |
rs7988701 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148061 | gccatgactatgttg[C/T]gtacaaatatctgtt | 221178 |
rs7988870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SPATA13 | GRCh38.p7 | 13:24245708 | gcaatcctcctgcct[C/T]ggcctcccaagtagc | 221178 |
rs7988904 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148172 | GACATTCCTGCACAG[C/G]ATTTGCAGTTGTAGT | 221178 |
rs7989087 | snp | A/C | 0.194278 | 0.243711 | intron-variant | SPATA13 | GRCh38.p7 | 13:24281925 | TGAACTCCTCCTCAT[A/C]ATGACAGCCCTGTCT | 221178 |
rs7989553 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | SPATA13 | GRCh38.p7 | 13:24041502 | ACAGATAAAGCTAAA[C/T]AAAATGTCAGTATCA | 221178 |
rs7989564 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24098906 | cactccagcctggca[A/G]cagagcgagactcca | 221178 |
rs7990442 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | SPATA13 | GRCh38.p7 | 13:24261676 | TCAAAGGAAGCCAGG[G/T]CTTCCAGGTGTGAGA | 221178 |
rs7990496 | snp | A/G | 0.451359 | 0.148171 | intron-variant | SPATA13 | GRCh38.p7 | 13:24015067 | GGCTAATTTTTTTGT[A/G]TTTTTAGTAGATAAC | 221178 |
rs7990616 | snp | A/G | 0.381113 | 0.21286 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138029 | TACTGGGCCAGGCGT[A/G]GTGGCTCGCGCATGT | 221178 |
rs7991134 | snp | A/G | 0.275197 | 0.248727 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138266 | AAGCTGGGATGCACC[A/G]TTCCAGTCCAGCCCA | 221178 |
rs7991169 | snp | A/C | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24138315 | CGTCTGAAAAAAAAA[A/C]AAAAAACAGTTTTAC | 221178 |
rs7991170 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138318 | CTGAAAAAAAAAAAA[A/C]AAACAGTTTTACTGA | 221178 |
rs7991171 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24138319 | TGAAAAAAAAAAAAA[A/C]AACAGTTTTACTGAA | 221178 |
rs7991257 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | SPATA13 | GRCh38.p7 | 13:24055338 | AAGATCCCAGATGCA[A/G]TCAGCATGCCTGGGT | 221178 |
rs7991559 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24057057 | AGCGTCTGGCTCttt[C/T]ttttttttttttctt | 221178 |
rs7991661 | snp | A/G | 0.472429 | 0.114129 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066224 | TGCTCACCCCAAAAT[A/G]CCAAGCCCCACCAGA | 221178 |
rs7992375 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | SPATA13 | GRCh38.p7 | 13:24057078 | TTTTTTTCTTTTTTT[A/T]AAAAATTTTATTATT | 221178 |
rs7992761 | snp | C/G | 0.493293 | 0.0575177 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200451 | CCATGTATGCACTGC[C/G]CAACCTGAAACGTGA | 221178 |
rs7992902 | snp | A/G | 0.290718 | 0.246662 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994737 | GTGTAGAGGAATAAA[A/G]AGCACTCAGTTTTGG | 221178 |
rs7993660 | snp | A/G | 0.00500837 | 0.0497906 | intron-variant | SPATA13 | GRCh38.p7 | 13:24294887 | AGTGGAAAGCACCCC[A/G]CATGATCCCATGCCA | 221178 |
rs7994230 | snp | A/G | 0.249038 | 0.249998 | intron-variant | SPATA13 | GRCh38.p7 | 13:24069985 | GAGATGTGGGAGTGC[A/G]GTAGAGGGGTCTCTG | 221178 |
rs7994294 | snp | A/G | 0.480382 | 0.097079 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066513 | ACAGGCCACCATTTT[A/G]CCACCCTGGGACAAA | 221178 |
rs7994320 | snp | G/T | 0.499971 | 0.00379382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121765 | TCATGACATCCCCTC[G/T]TGTTTCAGATTTCCA | 221178 |
rs7994350 | snp | A/C | 0.396727 | 0.202413 | intron-variant | SPATA13 | GRCh38.p7 | 13:24142419 | TTTTCTTTGTCTTTC[A/C]TGACCTTGACACTTT | 221178 |
rs7994554 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148306 | GTCTCAGTCCTACTT[A/T]CATGAGCCCCGTTGT | 221178 |
rs7994815 | snp | A/G | 0.177182 | 0.23916 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203917 | GTGTGTATATGCTGT[A/G]GCTCTGGATGATTAA | 221178 |
rs7994865 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149733 | ACCCAGAGGGAGAGC[A/G]GCTTGTACAAAGGCC | 221178 |
rs7995044 | snp | G/T | 0.491473 | 0.0647364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070458 | CTTGGCGTCTCTGGT[G/T]TGTTTTGGTCGTGGT | 221178 |
rs7995047 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155815 | ttgcaaaactgacat[C/T]ctgtccccattaagc | 221178 |
rs7995088 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291906 | ggactacaggcgccc[A/G]ccaccgcgcccggct | 221178 |
rs7995090 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SPATA13 | GRCh38.p7 | 13:23996360 | AAAATTCAGATAAGC[C/T]AGagaagaaaggctt | 221178 |
rs7995092 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24099268 | agcatctctttataa[C/T]atcattctatctaat | 221178 |
rs7995793 | snp | G/T | 0.231775 | 0.249335 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276572 | agttctgtcgtacaa[G/T]agtgtgaatatactt | 221178 |
rs7995893 | snp | A/G | 0.144969 | 0.226867 | intron-variant | SPATA13 | GRCh38.p7 | 13:24095010 | gagatttctcagaaa[A/G]ttaaaaatagaatcg | 221178 |
rs7996017 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24182912 | AAGAAGGCAAAGGCA[A/G]CTCACCGAGGGCTCA | 221178 |
rs7996166 | snp | A/G | 0.499974 | 0.00359416 | intron-variant | SPATA13 | GRCh38.p7 | 13:24121752 | AGAAAAGCTGCCTTC[A/G]TGACATCCCCTCGTG | 221178 |
rs7996973 | snp | C/G | 0.175576 | 0.238665 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103963 | ATTAGCTGATTAGGA[C/G]TGACTCTAAGTAGGG | 221178 |
rs7997126 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | SPATA13 | GRCh38.p7 | 13:24291757 | TTTTTTATTTTTTTA[A/T]TTTTTTTTTTGAGAC | 221178 |
rs7997140 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SPATA13 | GRCh38.p7 | 13:24070856 | aaatagcagctcttc[C/T]tggatctcagaactg | 221178 |
rs7997167 | snp | A/T | 0.348574 | 0.229746 | intron-variant | SPATA13 | GRCh38.p7 | 13:24045108 | TTTTGAAAATCACCC[A/T]ATGTATAATTTATAT | 221178 |
rs7997351 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24167196 | GTGTCCTGGCCATCA[C/T]GCAGGAAGTGCTTTG | 221178 |
rs7997542 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | SPATA13 | GRCh38.p7 | 13:24021750 | ggagtctcactctgt[C/T]gcccaggctggagtg | 221178 |
rs7997748 | snp | C/G | 0.171704 | 0.237423 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104392 | TTTTAGAGAGGTTTG[C/G]TTTTACAATTCTCAA | 221178 |
rs7998301 | snp | G/T | 0.116838 | 0.211584 | upstream-variant-2KB | SPATA13 | GRCh38.p7 | 13:23979482 | ATGCAACAGTAAGGG[G/T]TTGGGAGAAGGGAGA | 221178 |
rs7998390 | snp | A/G | 0.369958 | 0.21934 | intron-variant | SPATA13 | GRCh38.p7 | 13:24074654 | AAAAAAAAAACCCTT[A/G]TAGGAATTAGGGAAC | 221178 |
rs7998436 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SPATA13 | GRCh38.p7 | 13:24183063 | CTTGCCAGAAAAGAT[A/G]TAGAGAGATTGCTGC | 221178 |
rs7998538 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24105990 | aactgtgagaaatac[A/G]tttctgtcgtttaag | 221178 |
rs7999071 | snp | A/G | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24271283 | GCTGATATTGTTACT[A/G]GTTTTGCTGCTGATA | 221178 |
rs7999091 | snp | G/T | 0.228842 | 0.249103 | intron-variant | SPATA13 | GRCh38.p7 | 13:24257883 | ACAGCATGACCCAAA[G/T]TTTATGCCAACCAGC | 221178 |
rs7999200 | snp | G/T | 0.481087 | 0.0953875 | intron-variant | SPATA13 | GRCh38.p7 | 13:24066562 | ATCAAAGCAGAGGCA[G/T]TTCTCAAAGGCGGGA | 221178 |
rs7999364 | snp | A/G | 0.185155 | 0.241444 | intron-variant | SPATA13 | GRCh38.p7 | 13:24104234 | ACAATGTAAAGCTAG[A/G]ATGGGTTTTTTTTTT | 221178 |
rs7999402 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | SPATA13 | GRCh38.p7 | 13:24295367 | tgtaatcccagcact[C/T]tgggaggccaaagtg | 221178 |
rs7999639 | snp | A/G | 0.49621 | 0.0433651 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042872 | CCAGGGGAAACGTGC[A/G]TTTAAAAATAGTTCC | 221178 |
rs7999836 | snp | C/G | 0.49621 | 0.0433651 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042998 | AGAATGAACCCTTTC[C/G]CAATGTGTGTCTTAG | 221178 |
rs8000702 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SPATA13 | GRCh38.p7 | 13:24106098 | gagtgcagtggcaca[A/G]tcatggctcactgca | 221178 |
rs8000782 | snp | A/G | 0.497613 | 0.0344622 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003877 | ACAATATACATCAGC[A/G]AATACAGAACCCATT | 221178 |
rs8000800 | snp | A/C | 0.497641 | 0.0342639 | intron-variant | SPATA13 | GRCh38.p7 | 13:24003893 | AATACAGAACCCATT[A/C]AACAAGAACCAATAC | 221178 |
rs8001002 | snp | A/C | 0.496175 | 0.0435625 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042893 | AAATAGTTCCTCAGA[A/C]GCCTACTGTCTGTTT | 221178 |
rs8001153 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053374 | TCAACCACTCATTCC[A/G]TGGCTGATTCACGTG | 221178 |
rs8001551 | snp | A/G | 0.369754 | 0.219451 | intron-variant | SPATA13 | GRCh38.p7 | 13:24277361 | AGGCAGGAGAATGGC[A/G]TGAACCTAGGAGGCG | 221178 |
rs8001704 | snp | C/T | 0.177824 | 0.239355 | intron-variant | SPATA13 | GRCh38.p7 | 13:24203988 | TCAGTCATGCAAAAA[C/T]GTAACTTAATGTAAT | 221178 |
rs8001760 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | SPATA13 | GRCh38.p7 | 13:23983153 | catcacaaaacacca[C/T]agcctgggggcttaa | 221178 |
rs8002029 | snp | A/G | 0.137187 | 0.223099 | intron-variant | SPATA13 | GRCh38.p7 | 13:24092396 | CTGCCTTGCTCTTGC[A/G]TAGTTAGTGAATGAC | 221178 |
rs8002266 | snp | G/T | 0.485866 | 0.0828688 | intron-variant | SPATA13 | GRCh38.p7 | 13:24204284 | TGCAGATGAAAAATC[G/T]GAAGAAACACTGTGT | 221178 |
rs8002376 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SPATA13 | GRCh38.p7 | 13:24235703 | tcgaggccacagtga[A/G]ttatgattgcaccac | 221178 |
rs8002384 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SPATA13 | GRCh38.p7 | 13:24292190 | CCATCATTTCGTGCA[C/T]GCACAGAAGCCTTTG | 221178 |
rs8002750 | snp | C/T | 0.251296 | 0.249997 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276671 | ataaaatttactttt[C/T]aattattataataCA | 221178 |
rs8002758 | snp | A/T | 0.232651 | 0.249397 | intron-variant | SPATA13 | GRCh38.p7 | 13:24276889 | TGGCCATTGTGAGGA[A/T]CTCTGCCCAGCAGAG | 221178 |
rs8002868 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | SPATA13 | GRCh38.p7 | 13:24089145 | TCCACAGGGAATAAC[A/G]GAAGCACACGTAGGA | 221178 |
rs9318268 | snp | A/G | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24046626 | tagcaagagtttgtt[A/G]ttagttcctgtagct | 221178 |
rs9318271 | snp | A/G | 0.49607 | 0.0441545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24047006 | ctagtctaggtaggg[A/G]tttcatggctaattt | 221178 |
rs9318302 | snp | C/T | 0.432357 | 0.171014 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075642 | CAACGTTGCTTATCC[C/T]GCTTTTTAAAAGTTA | 221178 |
rs9318303 | snp | C/G | 0.463774 | 0.129618 | intron-variant | SPATA13 | GRCh38.p7 | 13:24079824 | ACATCTCCCCATTTC[C/G]CCTCTCACCTTTTGG | 221178 |
rs9318309 | snp | C/T | 0.396546 | 0.202545 | intron-variant | SPATA13 | GRCh38.p7 | 13:24085135 | TGCTTTTTCCCTTGT[C/T]TTGTTGAGACAGATT | 221178 |
rs9318313 | snp | A/G | 0.109814 | 0.206997 | intron-variant | SPATA13 | GRCh38.p7 | 13:24103234 | TTCCACAGATGCTAA[A/G]CCAGGTTATTACCAG | 221178 |
rs9318316 | snp | C/T | 0.474634 | 0.109726 | intron-variant | SPATA13 | GRCh38.p7 | 13:24110024 | TCTCGGATGCTCTTA[C/T]GCTTTTAGAATTGCA | 221178 |
rs9318333 | snp | A/T | 0.491629 | 0.0641526 | intron-variant | SPATA13 | GRCh38.p7 | 13:24131937 | CATATCCCCTCAGGG[A/T]ACCAATGTGCTCAGC | 221178 |
rs9318334 | snp | C/G | 0.488363 | 0.0753851 | intron-variant | SPATA13 | GRCh38.p7 | 13:24132034 | GAGATGCGCTTGAGT[C/G]ACAGACTGAGGCTTC | 221178 |
rs9318347 | snp | A/G | 0.469937 | 0.118861 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148154 | TTTCCCATATTTTTA[A/G]AAGACATTCCTGCAC | 221178 |
rs9318363 | snp | C/T | 0.489492 | 0.0717183 | intron-variant | SPATA13 | GRCh38.p7 | 13:24163855 | ACAAAGTTTCTTTCC[C/T]CTTCCTTTCCCTTGA | 221178 |
rs9318385 | snp | A/G | 0.475789 | 0.107327 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193851 | TGATGAAGTGGTCAC[A/G]ATGAGGAAGATGGAT | 221178 |
rs9318386 | snp | C/T | 0.466927 | 0.124269 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196963 | GCAAGCTGCTGAGTA[C/T]GGGGTGAGTAGTGAT | 221178 |
rs9318387 | snp | A/C | 0.466927 | 0.124269 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197026 | TAGAAATCTTAACTT[A/C]GTGATAAAAGTTACC | 221178 |
rs9318417 | snp | C/T | 0.426507 | 0.177046 | intron-variant | SPATA13 | GRCh38.p7 | 13:24226858 | AGAAAGTAGGACTAT[C/T]GCAGAGTACTTTCAG | 221178 |
rs9318423 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SPATA13 | GRCh38.p7 | 13:24237867 | tatatcacatatatt[A/G]tataatatatatcat | 221178 |
rs9318424 | snp | A/G | 0.5 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24238193 | CCAGACTCTTGCTCT[A/G]TCTCCCAGACTGGAG | 221178 |
rs9318427 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SPATA13 | GRCh38.p7 | 13:24243461 | CTTCTGTAAAAGTAC[A/G]TGCTAAGTATGCAGG | 221178 |
rs9318446 | snp | C/T | 0.261332 | 0.249743 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279855 | TCTCTTGCCCCTGGC[C/T]TCTGCCCCCCATCTC | 221178 |
rs9318447 | snp | C/T | 0.265727 | 0.249505 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279882 | TCTCCTGGCCAGGAC[C/T]GAGTCAGCCCACCCA | 221178 |
rs9318448 | snp | C/G | 0.26518 | 0.249539 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279892 | AGGACTGAGTCAGCC[C/G]ACCCATGAGCGCTTC | 221178 |
rs9318449 | snp | A/T | 0.260227 | 0.249791 | intron-variant | SPATA13 | GRCh38.p7 | 13:24279988 | ACCTCTCTTGTGATT[A/T]ACCTCAGCCAGAGTT | 221178 |
rs9318450 | snp | G/T | 0.266425 | 0.25328 | intron-variant | SPATA13 | GRCh38.p7 | 13:24280172 | GCGTACCACGACCCC[G/T]GGTAGAGCTGTTTTG | 221178 |
rs9318459 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | SPATA13 | GRCh38.p7 | 13:24290209 | ATTGGGAAGAGAGGT[A/G]TGTTGAAATGGGCAT | 221178 |
rs9507205 | snp | A/C | 0.39709 | 0.20215 | intron-variant | SPATA13 | GRCh38.p7 | 13:23981414 | AGGCTCTACTATGTG[A/C]TGTGTACAGTGCTAG | 221178 |
rs9507206 | snp | A/G | 0.348794 | 0.229651 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987788 | CTCCAACCCCTGGCA[A/G]CCACCATTCTACTTT | 221178 |
rs9507207 | snp | C/T | 0.348354 | 0.22984 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988025 | CACAGTTTACTGCAA[C/T]CTGTGTCTGCTGAGT | 221178 |
rs9507208 | snp | C/T | 0.29789 | 0.24537 | intron-variant | SPATA13 | GRCh38.p7 | 13:23988213 | TGGCCTCCTGAAGTG[C/T]TGGGATTACAGGCGT | 221178 |
rs9507210 | snp | A/G | 0.287606 | 0.247155 | intron-variant | SPATA13 | GRCh38.p7 | 13:23994499 | GGAGGAGGTTCGTGT[A/G]TGGGACTGGCCGGCA | 221178 |
rs9507211 | snp | G/T | 0.300421 | 0.244863 | intron-variant | SPATA13 | GRCh38.p7 | 13:23997224 | gttaaggtataatgg[G/T]catagaatgcacata | 221178 |
rs9507212 | snp | A/C | | | intron-variant | SPATA13 | GRCh38.p7 | 13:23999366 | agatcctcattttct[A/C]ccaaaaaaaaaaaaa | 221178 |
rs9507214 | snp | G/T | 0.407502 | 0.194147 | intron-variant | SPATA13 | GRCh38.p7 | 13:24022653 | AAAATAAGAATTTTT[G/T]GGGGCTAAAACAAGA | 221178 |
rs9507215 | snp | G/T | 0.133777 | 0.221342 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025544 | aaaaataatccaaac[G/T]cttctccaaagtagt | 221178 |
rs9507216 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025685 | aaatggattttatta[C/T]ggtttaaattttcct | 221178 |
rs9507217 | snp | C/G | 0.533348 | 0.0891207 | intron-variant | SPATA13 | GRCh38.p7 | 13:24025891 | ctcactacaacctcc[C/G]cctcccaggttcaaa | 221178 |
rs9507219 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SPATA13 | GRCh38.p7 | 13:24027993 | TATAATTCTGTTTTA[C/G]TAGtttttaatttct | 221178 |
rs9507221 | snp | A/G | 0.46754 | 0.123192 | intron-variant, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:24033516 | TCTTGGTTTCAGCTC[A/G]GACTGACCTGGAAGA | 221178 |
rs9507222 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038052 | GAGTAGCTGGGATTA[C/T]AGGCGCCTGCCACCA | 221178 |
rs9507223 | snp | G/T | 0.482757 | 0.0912364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24038339 | CCTCGATTGTGCCAG[G/T]GGGCTTTAGTTCCCT | 221178 |
rs9507224 | snp | A/T | 0.106278 | 0.204558 | intron-variant | SPATA13 | GRCh38.p7 | 13:24039323 | GTTGACAGCTCTACC[A/T]TGCAGACTTTCGTGG | 221178 |
rs9507225 | snp | C/T | 0.498133 | 0.030494 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042398 | TTGTGGAAAGATCCA[C/T]AGGCCGCTTTCTGAG | 221178 |
rs9507226 | snp | A/G | 0.138546 | 0.223781 | intron-variant | SPATA13 | GRCh38.p7 | 13:24042607 | TCAGAGCACTGGCTC[A/G]TGGGCGGTCAGCTGG | 221178 |
rs9507227 | snp | G/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24044895 | cagaggagggggtgg[G/T]gTTCTTCCTTTATTC | 221178 |
rs9507228 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053073 | TTATTGTTTTGTTTC[A/G]ATTTTCTGAGACCTA | 221178 |
rs9507229 | snp | A/G | 0.136847 | 0.222927 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053101 | CTATCCGTACCTAGA[A/G]CACAAACTTGTTTTT | 221178 |
rs9507230 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053335 | GATGCAAATATCTAG[C/T]GAACTCTAGGCCGCT | 221178 |
rs9507231 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SPATA13 | GRCh38.p7 | 13:24053358 | AGGCCGCTAAAACTT[C/T]TCAACCACTCATTCC | 221178 |
rs9507233 | snp | A/C | 0.496681 | 0.0405994 | intron-variant | SPATA13 | GRCh38.p7 | 13:24060417 | tcccttccttacacc[A/C]tgtaaaaatgtaact | 221178 |
rs9507234 | snp | C/G | 0.197393 | 0.244402 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065381 | GAGGGCTGTGAGCCT[C/G]CTTATGTTCCTCCAC | 221178 |
rs9507235 | snp | A/G | 0.225005 | 0.248747 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065456 | TGCTCTGGAAATACA[A/G]CCACCTGTAGCTCTG | 221178 |
rs9507236 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SPATA13 | GRCh38.p7 | 13:24065513 | CTTACCCCAGCCAAC[A/G]CTGAGAACTCACTGA | 221178 |
rs9507239 | snp | A/T | 0.256619 | 0.249912 | intron-variant | SPATA13 | GRCh38.p7 | 13:24075770 | AAAAAAGTGGACGGG[A/T]AGCACTGTTCTTTCT | 221178 |
rs9507240 | snp | C/T | 0.237593 | 0.249692 | intron-variant | SPATA13 | GRCh38.p7 | 13:24094783 | GTCTAAAAATTAATA[C/T]GTAAAATATTTCAGA | 221178 |
rs9507241 | snp | C/T | 0.332568 | 0.235971 | intron-variant | SPATA13 | GRCh38.p7 | 13:24101067 | CCTGGTGGACACTCT[C/T]AAGGGGAAATTCGCA | 221178 |
rs9507242 | snp | C/T | | | intron-variant | SPATA13 | GRCh38.p7 | 13:24102120 | gtagggttccaattt[C/T]ttcacatccttagca | 221178 |
rs9507243 | snp | C/T | 0.38286 | 0.211774 | intron-variant | SPATA13 | GRCh38.p7 | 13:24102765 | aggcatgagccacca[C/T]gcccagccacttcac | 221178 |
rs9507245 | snp | G/T | 0.450483 | 0.149354 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114669 | TTTTTTGTTGTTGTT[G/T]TTGTTGTTTTGAGAT | 221178 |
rs9507246 | snp | C/T | 0.479095 | 0.100076 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114731 | GCAATGGCACGATCT[C/T]GGCTCACCACAACTT | 221178 |
rs9507247 | snp | A/G | 0.382473 | 0.212016 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114979 | TTGGCTTTGTTTTGA[A/G]CCCAGCCCAGGTTGA | 221178 |
rs9507248 | snp | C/T | 0.499968 | 0.00399348 | intron-variant | SPATA13 | GRCh38.p7 | 13:24114999 | GCCCAGGTTGAGTCC[C/T]GGTGACTCTGACAGG | 221178 |
rs9507249 | snp | C/T | 0.499971 | 0.00379382 | intron-variant | SPATA13 | GRCh38.p7 | 13:24115038 | CCAGAAACATTGTTT[C/T]AGGGGAGGAGACAAG | 221178 |
rs9507251 | snp | A/T | 0.371785 | 0.218331 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130041 | AGGAGGCTACTCCAC[A/T]CAGCCCTTTCCTTCA | 221178 |
rs9507252 | snp | A/G | 0.349233 | 0.229462 | intron-variant | SPATA13 | GRCh38.p7 | 13:24130972 | GGGGTGGAGCGGGGG[A/G]CGCTTTCTGGCTTCA | 221178 |
rs9507253 | snp | A/C | 0.496999 | 0.0386216 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135603 | CTCGGGAGGCTGAGG[A/C]AGGAGAATGGCGTGA | 221178 |
rs9507255 | snp | A/C | 0.49706 | 0.0382258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24135689 | GGCGACAGAGCAAGA[A/C]TCCGTCTCAAAAAAA | 221178 |
rs9507258 | snp | C/T | 0.379158 | 0.214052 | intron-variant | SPATA13 | GRCh38.p7 | 13:24143350 | TCTCCCATTTTTCCC[C/T]AATATTAAAGTAAAA | 221178 |
rs9507259 | snp | C/G | 0.481242 | 0.0950111 | intron-variant | SPATA13 | GRCh38.p7 | 13:24148670 | GAGAATCTCTGCAAG[C/G]AACTGGCTCAGTCTT | 221178 |
rs9507260 | snp | A/G | 0.49681 | 0.0398085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24149793 | GGGTCAGGTTGTCAC[A/G]GGCCTTGCATGACAT | 221178 |
rs9507261 | snp | A/C | 0.459233 | 0.136827 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152394 | TCAGTGGTTCCTGCT[A/C]AAGGACATGGCCACT | 221178 |
rs9507262 | snp | G/T | 0.304688 | 0.243945 | intron-variant | SPATA13 | GRCh38.p7 | 13:24152887 | TGTTCAGAACTCAAA[G/T]GATGATTATTTCTTT | 221178 |
rs9507263 | snp | A/T | 0.441568 | 0.160629 | intron-variant | SPATA13 | GRCh38.p7 | 13:24155998 | GTCCACCTGTGTTGC[A/T]GCGTGTGTCGGAATT | 221178 |
rs9507264 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | SPATA13 | GRCh38.p7 | 13:24164107 | CTTGAGGGAAACTAT[A/G]TAATACATGGCAATT | 221178 |
rs9507266 | snp | C/G | 0.450609 | 0.149185 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192131 | cccagtccattgtgg[C/G]catgctcagacaagg | 221178 |
rs9507267 | snp | C/G | 0.454302 | 0.144085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24192240 | ggacccccctccccc[C/G]acaccttatctgcct | 221178 |
rs9507268 | snp | A/G | 0.453939 | 0.144598 | intron-variant | SPATA13 | GRCh38.p7 | 13:24193509 | GCTTCACCTGGAGCC[A/G]AGAATGGGTGATGTG | 221178 |
rs9507269 | snp | A/G | 0.454182 | 0.144256 | intron-variant | SPATA13 | GRCh38.p7 | 13:24194640 | ATTGATTCACCACTC[A/G]CCGACTGGTCTGCCG | 221178 |
rs9507270 | snp | C/T | 0.454302 | 0.144085 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195158 | CCTGCCTCCTGTCTC[C/T]ATGGATTTGCCTATT | 221178 |
rs9507271 | snp | G/T | 0.453575 | 0.145111 | intron-variant | SPATA13 | GRCh38.p7 | 13:24195280 | ttgtagcatagcatg[G/T]gtcagtacttctgtt | 221178 |
rs9507272 | snp | A/G | 0.468148 | 0.122112 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196271 | TTCCCTAAGAGTGAG[A/G]CTTGGCATAAACCCT | 221178 |
rs9507273 | snp | A/G | 0.467132 | 0.12391 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196734 | ACAGAGTGAGACCCT[A/G]TGTCAAAACAAAACA | 221178 |
rs9507274 | snp | C/G | 0.482384 | 0.0921818 | intron-variant | SPATA13 | GRCh38.p7 | 13:24196736 | AGAGTGAGACCCTAT[C/G]TCAAAACAAAACAAA | 221178 |
rs9507276 | snp | A/T | 0.413083 | 0.189483 | intron-variant | SPATA13 | GRCh38.p7 | 13:24197776 | TTTAAAAAATATGTA[A/T]AAGGATTAGTGAGGG | 221178 |
rs9507278 | snp | A/C | 0.475613 | 0.107697 | intron-variant | SPATA13 | GRCh38.p7 | 13:24200511 | CTCGTTCTCAGCCCC[A/C]AGTCTCCCACCCAAG | 221178 |
rs9507279 | snp | A/C | 0.32153 | 0.239548 | intron-variant | SPATA13 | GRCh38.p7 | 13:24201696 | cgcccaccttggcct[A/C]ccaaaatgctgagat | 221178 |
rs9507281 | snp | C/T | 0.157311 | 0.232183 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206680 | gtggatcacctgagg[C/T]caggagttcaagacc | 221178 |
rs9507282 | snp | A/G | 0.157311 | 0.232183 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206825 | tgaacccagggggca[A/G]aggttgcagtaagct | 221178 |
rs9507283 | snp | A/G | 0.158302 | 0.232576 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206836 | ggcaaaggttgcagt[A/G]agctgagattgtgct | 221178 |
rs9507284 | snp | C/T | 0.17138 | 0.237316 | intron-variant | SPATA13 | GRCh38.p7 | 13:24206840 | aaggttgcagtaagc[C/T]gagattgtgctattg | 221178 |
rs9507285 | snp | C/G | 0.291235 | 0.246576 | intron-variant | SPATA13 | GRCh38.p7 | 13:24210750 | gaatcttttatggtt[C/G]tatatgaattttagg | 221178 |
rs9507286 | snp | C/T | 0.290718 | 0.246662 | intron-variant | SPATA13 | GRCh38.p7 | 13:24211331 | atccttatcttattt[C/T]tgatgctagaggaaa | 221178 |
rs9507287 | snp | C/T | 0.291235 | 0.246576 | intron-variant | SPATA13 | GRCh38.p7 | 13:24212439 | CCTTGCTTCATGTGG[C/T]CCTGAAGTGCTTATG | 221178 |
rs9507291 | snp | C/T | 0 | 0 | intron-variant | SPATA13 | GRCh38.p7 | 13:24241211 | ATTATTTATTTTTAC[C/T]TACAAGCCATAGAAA | 221178 |
rs9507292 | snp | C/T | 0.254944 | 0.249951 | intron-variant | SPATA13 | GRCh38.p7 | 13:24244846 | GGCAACAGAGTGAGA[C/T]TGTCGCAAAATAAAT | 221178 |
rs9507294 | snp | C/T | 0.493793 | 0.055364 | intron-variant | SPATA13 | GRCh38.p7 | 13:24249209 | TATCATAGCTCATCA[C/T]TGGTCACCAAACCAC | 221178 |
rs9507299 | snp | A/G | 0.451856 | 0.147493 | intron-variant | SPATA13 | GRCh38.p7 | 13:24285052 | TACCTCCAGCTTTTG[A/G]CATTCTTGAGCAGAA | 221178 |
rs9507300 | snp | A/G | 0.346147 | 0.230772 | intron-variant | SPATA13 | GRCh38.p7 | 13:24286102 | CCAAATGCCACCAGC[A/G]TATCCAAGTGAGAGG | 221178 |
rs9510982 | snp | A/G | 0.32768 | 0.237625 | utr-variant-5-prime, nc-transcript-variant | SPATA13 | GRCh38.p7 | 13:23979722 | GGGGAGCCAGAGACT[A/G]ATTCGCTGCGGTCCT | 221178 |
rs9510983 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SPATA13 | GRCh38.p7 | 13:23980161 | cgccactccatcctc[A/G]gcgacagagcgagac | 221178 |
rs9510985 | snp | C/T | 0.29789 | 0.24537 | intron-variant | SPATA13 | GRCh38.p7 | 13:23987805 | CACCATTCTACTTTC[C/T]GTCTCTATGAATTTG | 221178 |
rs9510987 | snp | G/T | 0.279461 | 0.248258 | intron-variant | SPATA13 | GRCh38.p7 | 13:24001104 | ACACAGTTCTTCCAG[G/T]CTGGCCGAGTGGCCT | 221178 |
rs9510988 | snp | A/T | 0.260504 | 0.249779 | intron-variant | SPATA13 | GRCh38.p7 | 13:24004772 | AAAGCTGTGGGAGAG[A/T]CTACAGTGACAGTAG | 221178 |
rs9510989 | snp | A/T | 0.242775 | 0.249896 | intron-variant | SPATA13 | GRCh38.p7 | 13:24008401 | CCCTGGGGCTGGCTG[A/T]TCTTGACGCTGATGC | 221178 |
rs9510990 | snp | A/G | 0.342358 | 0.232314 | intron-variant | SPATA13 | GRCh38.p7 | 13:24009607 | aaaattttctgaatg[A/G]caattgattgaaaga | 221178 |
rs9510991 | snp | A/G | 0.470034 | 0.11868 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012143 | GCCAGGTGTGTAACC[A/G]GCCTATGATGAAAGC | 221178 |
rs9510992 | snp | C/G | 0.242481 | 0.250607 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012387 | CACCAGCAGATGCTC[C/G]TGGTTGGTCAGTATC | 221178 |
rs9510993 | snp | C/T | 0.29278 | 0.246313 | intron-variant | SPATA13 | GRCh38.p7 | 13:24012444 | ACCATTAGGGTGTCC[C/T]CTAGTACAACAGGAC | 221178 |
rs9510995 | snp | A/G | 0.482534 | 0.0918038 | intron-variant | SPATA13 | GRCh38.p7 | 13:24016216 | CCTCCTGTGAGGGGT[A/G]GAGGCCAGTGGGGTC | 221178 |