SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12577 | snp | A/T | 0 | 0 | missense, intron-variant | ZFAND6 | GRCh38.p7 | 15:80131235 | TTTTTGTTTCGGTTT[A/T]TCAAGAGACTTGCTT | 54469 |
rs12890 | snp | C/T | 0 | 0 | missense | ZFAND6 | GRCh38.p7 | 15:80137608 | TCTTTTGGATCTTTT[C/T]ACCAACAACTACTGG | 54469 |
rs15416 | snp | A/G | | | stop-gained, intron-variant | ZFAND6 | GRCh38.p7 | 15:80131245 | AGCGATTCTTTTTTT[A/G]TTTCGGTTTTTCAAG | 54469 |
rs870184 | snp | G/T | 0.492727 | 0.0598633 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80098716 | TTTTCTGGTGGGTAG[G/T]ATACTGAGGGTGGAG | 54469 |
rs870185 | snp | A/G | 0.495252 | 0.0484902 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80098915 | GCATTGATTTCAGCC[A/G]TTTAAAGTTAATATT | 54469 |
rs870994 | snp | C/T | 0.41507 | 0.187755 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80071904 | TACTGGGCAGAAATA[C/T]TATTACATTTAACAG | 54469 |
rs934003 | snp | C/T | 0.493201 | 0.0579089 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80121593 | TGAACCAACATACTA[C/T]ATATTAAAAGAAAAC | 54469 |
rs939969 | snp | A/G | 0.439641 | 0.162899 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80099128 | AAAAATAAAATTGGC[A/G]AATTTAAAAAACTTT | 54469 |
rs939974 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80090739 | AGAACTCCTATTTAG[A/G]ACTTTGAAACCTGAG | 54469 |
rs939975 | snp | A/G | 0.127944 | 0.218179 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80071863 | TGAGTATTTTGCCAA[A/G]GTTAATGCTTAACCA | 54469 |
rs1056018 | snp | C/T | 0.496517 | 0.0415876 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80132592 | gtgccgattaaaatg[C/T]gtggcattttaagtg | 54469 |
rs1140650 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80059782 | GGCGGCGGCGCGCAG[C/T]GTGTCAGGCGGAGAG | 54469 |
rs1357335 | snp | A/T | 0.493013 | 0.058691 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80076521 | TCATATCTGTTTTTC[A/T]CTGCTTCATATTCGT | 54469 |
rs1357336 | snp | C/T | 0.492918 | 0.0590819 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80076556 | GAATACTAGCTAGAG[C/T]GAAGAATAACACCAG | 54469 |
rs1403251 | snp | A/C | 0.154329 | 0.23097 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80100717 | GCTCAAATACATTTA[A/C]AAATCTAAGCAAAAC | 54469 |
rs1522635 | snp | A/T | 0.397633 | 0.201754 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80123600 | TTAAAAATTTAGCCA[A/T]CTTAAACTAGGATTG | 54469 |
rs1522636 | snp | C/G | 0.391325 | 0.206222 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80121831 | ATTAGAATTCAGAGA[C/G]TACATCTTACCTGGG | 54469 |
rs1533857 | snp | A/G | 0.447421 | 0.153379 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80105157 | TATAACTGTAAAGGA[A/G]GGATAAAAGCAAGTA | 54469 |
rs1879892 | snp | C/T | 0.413914 | 0.188765 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80120769 | CCTTACTTTCCAAGA[C/T]ACTTGAGGTGTCCCC | 54469 |
rs1916048 | snp | A/G | 0.394904 | 0.203722 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80120237 | ATGATAAAGAAAAAA[A/G]CCCACATATATCAAA | 54469 |
rs1983414 | snp | C/T | 0.411242 | 0.191052 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80090995 | CAAGATAGAATATTT[C/T]AGTAGAAAAACATAA | 54469 |
rs2030555 | snp | C/T | 0.126564 | 0.217402 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80106426 | TCAATTTCGCCTTTA[C/T]AGTAAAAAAGAAGCC | 54469 |
rs2030556 | snp | A/G | 0.154329 | 0.23097 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80106403 | AAGAAGCCACAGACA[A/G]TAAGTAAATGAATAG | 54469 |
rs2103043 | snp | C/T | 0.49703 | 0.0384237 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80133741 | aagttagacgatctc[C/T]tcctgccttaagtcc | 54469 |
rs2114714 | snp | A/G | 0.406814 | 0.194704 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80134378 | agatgcttctctggg[A/G]gcaagcatttatcac | 54469 |
rs2114715 | snp | C/G | 0.421209 | 0.182174 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80133410 | gtcaggagtttgaga[C/G]cagcctggccaacgt | 54469 |
rs2140155 | snp | A/C | 0.399253 | 0.200558 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80136867 | TTCAGAATTAAATTC[A/C]TTCCTCATTTAATCC | 54469 |
rs2461639 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80075814 | CGACAAAACTGTTTC[A/G]AGTTCATTTTCTCCG | 54469 |
rs2461640 | snp | C/G | 0.439085 | 0.163545 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80074266 | AGATACAATTGCTCA[C/G]TTAAGTGGGTAAAAG | 54469 |
rs2461641 | snp | C/T | 0.457388 | 0.139608 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80072414 | AGACACACTAAAACC[C/T]CCTGGATAAGCTGGT | 54469 |
rs2461642 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80071105 | AATATGGAGCAATAC[C/T]CTGCTGAAGCCCAAA | 54469 |
rs2461649 | snp | A/G | 0.305186 | 0.243833 | upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80058827 | CTATTGTGAATGAGG[A/G]GTTCCGTTAGGGCAT | 54469 |
rs2469600 | snp | C/G | 0.447162 | 0.153712 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80075489 | CCTTGTAGAAAACTA[C/G]TTTCCACTCTCCCTA | 54469 |
rs2469604 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80076289 | ACAATCAGATTCTGG[C/T]TTGGGTGGCAGTATC | 54469 |
rs2866367 | snp | G/T | 0.485596 | 0.0836329 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80073403 | GACGTAATTGTAGTG[G/T]ATTTCAGTACAAGAA | 54469 |
rs2866368 | snp | C/T | 0.126564 | 0.217402 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80096814 | CATATAGGGGAAAGG[C/T]AGTTATCTCAGTATT | 54469 |
rs2866369 | snp | G/T | 0.46014 | 0.13543 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80127455 | tagctggctgtgatg[G/T]catgcgcctgtagtc | 54469 |
rs2903265 | snp | A/G | 0.45843 | 0.138046 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80121042 | TGTTTCAGTAGTTGT[A/G]TAAGAAGGATCATGC | 54469 |
rs2903266 | snp | A/G | 0.460365 | 0.13508 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80127574 | cagcctgggcaaaag[A/G]gcaaaactccatctc | 54469 |
rs2957043 | snp | A/T | | | intron-variant | ZFAND6 | GRCh38.p7 | 15:80065538 | aaaaaaaaaaaaaaa[A/T]TCAAAACCAAAACTA | 54469 |
rs3082079 | in-del | -/TTTTTTT/TTTTTTTT | 0 | 0 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80099634 | ttttttttttttttt[-/TTTTTTT/TTTTTTTT]cgagacggagtctca | 54469 |
rs3082081 | in-del | -/T/TT | | | intron-variant | ZFAND6 | GRCh38.p7 | 15:80106599 | GTTTTTTTTTTTTTT[-/T/TT]GCTTCCATATTATAG | 54469 |
rs3082115 | in-del | -/T/TT | 0 | 0 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80133200 | TTTGTTTTTTTTTTT[-/T/TT]GAAATGGAGTCTTGC | 54469 |
rs3784761 | snp | A/C | 0.128632 | 0.218563 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80124871 | TCCAGTATGTAAAAT[A/C]TCTTAACAACCTAGT | 54469 |
rs3784762 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80130932 | AAGTACAGTTAAAAC[C/G]TAAAGAAAGTCTATA | 54469 |
rs3858955 | snp | A/G | 0.498673 | 0.0257246 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80128183 | TACTCATTAGCAATT[A/G]CTCCCCACTTCCCAC | 54469 |
rs3974671 | in-del | -/A/AA/TTTTAA | 0.491473 | 0.0647364 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80132941 | GTAAGGACTATTGTT[-/A/AA/TTTTAA]AAAAAAAAAAAAAAA | 54469 |
rs4594222 | snp | A/G | 0.487621 | 0.0776941 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80124035 | AAATATTCTAGTCCC[A/G]TCTAGCATATTGTGA | 54469 |
rs4778580 | snp | A/G | 0.415563 | 0.18732 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80070819 | TTTTTTTTTCTTCCC[A/G]TAAAACCTTTGGCCA | 54469 |
rs4778581 | snp | C/T | 0.47885 | 0.100637 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80070911 | TTGCTTCTGTACCTC[C/T]TCTGCTTCCAGTGTT | 54469 |
rs4778582 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80128624 | ATTCATTTGGTGACT[A/G]TTGAAATTCAGGTTG | 54469 |
rs4778744 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80063537 | gctgagactacagac[A/G]tgcaccaccacgccc | 54469 |
rs4778745 | snp | A/G | 0.150333 | 0.229274 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80071071 | GTCCACTTAAAGGGC[A/G]TAATAGATTATGCAG | 54469 |
rs4778746 | snp | A/G | 0.449726 | 0.150364 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80089680 | TAGACTCCATTGCCT[A/G]TGGAAATGGAATAGC | 54469 |
rs4778747 | snp | A/G | 0.121369 | 0.214369 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80103578 | TTGAGTTTGCTCTTA[A/G]TCAAGAACTTAAAGT | 54469 |
rs4778748 | snp | C/G | 0.152001 | 0.229992 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80108287 | GAAGATTTACCTTAG[C/G]GGGAGAAGAGATTTT | 54469 |
rs4778752 | snp | A/G | 0.439224 | 0.163383 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80112314 | GTACAGTAGTCCAAA[A/G]TCCCTATACTTTTAT | 54469 |
rs4778754 | snp | C/T | 0.398354 | 0.201224 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80128858 | TGAGATATGCAGTAG[C/T]ATTTGTATGCATAGA | 54469 |
rs6495471 | snp | A/G | 0.437683 | 0.165152 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80062811 | TGATAGATAACTATT[A/G]TTAACATTTTGTCAG | 54469 |
rs6495472 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80079750 | tgcctcccaggttca[C/T]gccatcctcctgcct | 54469 |
rs6495473 | snp | G/T | 0.419296 | 0.183954 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80080183 | ttgtattttagtagc[G/T]acggggtttcaccat | 54469 |
rs6495474 | snp | G/T | 0.457504 | 0.139435 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80085110 | CTGATTCTTCCATAC[G/T]TCATACCAGGAGGTT | 54469 |
rs6495475 | snp | A/G | 0 | 0 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80127720 | attgtcaaggatgta[A/G]aaaaattggagccct | 54469 |
rs7164584 | snp | G/T | 0 | 0 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80068139 | gcctgtttttttttt[G/T]tttgtttgtttgttt | 54469 |
rs7166132 | snp | C/T | 0.231482 | 0.249313 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80115894 | CTATGACTTTTTACT[C/T]GAGTTTTTATGGAAA | 54469 |
rs7166509 | snp | A/T | 0.227369 | 0.248974 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80080823 | caaaagccaggagct[A/T]aagagagtggggtgc | 54469 |
rs7168791 | snp | A/C | 0.444799 | 0.156695 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80107345 | ttaGGTAGTCATTAC[A/C]TAATGACATCACCAT | 54469 |
rs7169038 | snp | A/G | 0.460365 | 0.13508 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80126414 | acagtaatcaagact[A/G]tgttgtaccggcatg | 54469 |
rs7169400 | snp | A/G | 0.445724 | 0.155538 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80107396 | CATATAACGACAACT[A/G]TACTATTAtagtatg | 54469 |
rs7172637 | snp | A/T | 0.498852 | 0.0239341 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80136233 | gcacttcgggaggcc[A/T]aggcaggcagatcac | 54469 |
rs7173967 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80105004 | TCATTCTAAGGTGGT[A/G]GGATTCCCTGTTGCT | 54469 |
rs7175035 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80090598 | TCCATGCTCATCCCA[C/T]GTTTTTGTTTGTTTT | 54469 |
rs7175982 | snp | A/G | 0.48178 | 0.0936921 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80136401 | acgcaggaggcggag[A/G]ttgtggtgagccgag | 54469 |
rs7176220 | snp | A/G | 0.456568 | 0.140818 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80136541 | GAAGGGTGAGATTTA[A/G]TAATTTTCATCTTGT | 54469 |
rs7183846 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80088973 | TAATAGACCCACCAT[A/G]ATCTTGCCCTTGCTT | 54469 |
rs7183862 | snp | A/G | 0.373598 | 0.21731 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80088994 | GCCCTTGCTTATCTC[A/G]GTATCCTCATCTCAA | 54469 |
rs7183963 | snp | C/T | 0.198014 | 0.244535 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80097450 | gtcaggaatttgaga[C/T]cagccctgccgatat | 54469 |
rs8025843 | snp | C/T | 0.487621 | 0.0776941 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80134371 | cgtcgaagtgataaa[C/T]gcttgctcccagaga | 54469 |
rs8026552 | snp | A/T | 0.409552 | 0.192466 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80064647 | ATGTTTGGGTTTTTT[A/T]AAATGTTTTTTGAGA | 54469 |
rs8026715 | snp | A/G | 0.211516 | 0.24702 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80086132 | caacctccgtctgcc[A/G]ggttcgagtgattct | 54469 |
rs8034821 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80066233 | GATGATCTGAGACTG[C/T]CTCTCTGAGGATGTC | 54469 |
rs8034878 | snp | G/T | 0.455977 | 0.141681 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80060798 | GTGGTGGCGGGCGCC[G/T]GTAGTCCCAGCTACT | 54469 |
rs8035077 | snp | C/T | 0.219349 | 0.248114 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80124067 | AAATTCTTAAATGTT[C/T]TAAGTGAATAATTCT | 54469 |
rs8037703 | snp | A/G | 0.440471 | 0.161928 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80118145 | atttatttttgagac[A/G]gagtcttgctctgtt | 54469 |
rs8038958 | snp | C/T | 0.49168 | 0.063958 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80118084 | tataCATACTATATA[C/T]ACACACATTATACAT | 54469 |
rs8042120 | snp | C/T | 0.49121 | 0.0657086 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80118274 | actacaggcacacgc[C/T]gccacacccggctag | 54469 |
rs8042747 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80088421 | AAAAATACAAAATTA[A/G]GGGGTGTGGTGGTGC | 54469 |
rs9302291 | in-del | -/ACAC | 0.48033 | 0.0972021 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80064608 | TACACATGTATACAT[-/ACAC]ACACACACACACACA | 54469 |
rs9744611 | snp | A/C | 0.278995 | 0.248313 | intron-variant, upstream-variant-2KB | ZFAND6 | GRCh38.p7 | 15:80097673 | ATAAATAAATAAATA[A/C]ATACATACATTTATT | 54469 |
rs9920107 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80079123 | ttaatgggattattt[A/G]tttcttgcttgttga | 54469 |
rs10047974 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80127397 | gttggagaccagctt[C/G]gccaacatggtgaaa | 54469 |
rs10152983 | snp | C/T | 0.401215 | 0.199083 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80078289 | agtgcttagttccca[C/T]ttataagtgacaacg | 54469 |
rs10163055 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80075939 | CAATAGATTTTTGTA[A/G]GTACTAGATTTCTCA | 54469 |
rs10519277 | snp | A/G | 0.128632 | 0.218563 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80081346 | ACATACTGTTTGATA[A/G]AAGTAGGGGATATGA | 54469 |
rs10519280 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80100347 | AGAGAGGCCTTTGGA[A/G]CATACTAATGAAACT | 54469 |
rs10519281 | snp | C/T | 0.21303 | 0.247251 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80113654 | TCAACAGAATATAGC[C/T]GTTTTTTGCCTGACA | 54469 |
rs10851925 | snp | A/C | 0.476314 | 0.106217 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80106556 | ATAACTCTGAAAAAA[A/C]CAAATAATTTTTTCA | 54469 |
rs11072878 | snp | A/G | 0.393065 | 0.205018 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80064400 | CTTCCCTTTCTATAG[A/G]AATCATCATATATTT | 54469 |
rs11072879 | snp | G/T | 0.457271 | 0.139781 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80094783 | agttttcccattaat[G/T]ttttttttcttttgt | 54469 |
rs11072880 | snp | A/T | 0.41023 | 0.191902 | intron-variant | ZFAND6 | GRCh38.p7 | 15:80106571 | CCAAATAATTTTTTC[A/T]GTATGTTAAATTTGT | 54469 |