SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193224 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58814591 | aggagttcgagacca[C/G]cctgagcaatatggc | 54629 |
rs347111 | snp | C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58848629 | cctcccgagtagctg[C/G]gactacaggcgcccg | 54629 |
rs347112 | snp | A/G | 0.479984 | 0.0980171 | intron-variant | FAM63B | GRCh38.p7 | 15:58813579 | ttggtgggttatatc[A/G]taGttgcttgttggt | 54629 |
rs347113 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58816078 | caatatttacttatg[C/T]gccaggcactgttct | 54629 |
rs347114 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | FAM63B | GRCh38.p7 | 15:58832606 | tgaggcggaggttgc[G/T]gtgaactgaaatcac | 54629 |
rs347115 | snp | A/G | 0.462253 | 0.132093 | intron-variant | FAM63B | GRCh38.p7 | 15:58790760 | accaaaaatgagata[A/G]tccttgactccactt | 54629 |
rs347116 | snp | A/C | 0.194954 | 0.245711 | intron-variant | FAM63B | GRCh38.p7 | 15:58790588 | cttgtcttacccccc[A/C]ctaaggtctattgtc | 54629 |
rs364439 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58821078 | ACTTAAACTTTTAAG[C/T]TATAGGAAAATAAAA | 54629 |
rs367267 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | FAM63B | GRCh38.p7 | 15:58838111 | CAAGATATACTTTCA[G/T]GCCAGGTGTGGTGTG | 54629 |
rs374865 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58791543 | gattgcttgggcctg[A/G]gatccagaggctgca | 54629 |
rs379879 | snp | G/T | 0.391024 | 0.206427 | intron-variant | FAM63B | GRCh38.p7 | 15:58778977 | ATGTTGGCCAGGCTG[G/T]TCTTGAACTCCTGAC | 54629 |
rs384322 | snp | A/C | 0.0551013 | 0.156571 | intron-variant | FAM63B | GRCh38.p7 | 15:58788663 | ATTTATATATTTATA[A/C]TATCACCAAATAGGA | 54629 |
rs387812 | snp | C/T | 0.431177 | 0.172264 | intron-variant | FAM63B | GRCh38.p7 | 15:58782587 | TTTCCTCATCGTGCT[C/T]CACTTTTCACTGGTC | 54629 |
rs392739 | snp | C/T | 0.0352966 | 0.128072 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58859134 | TTTGGGAAGAGATCA[C/T]GCCATACTCAAAGAA | 54629 |
rs395601 | snp | C/G | 0.420733 | 0.18262 | upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770997 | ACAAGGGAGCTGCCC[C/G]GGAGTTCAACTTCCG | 54629 |
rs406699 | snp | A/G | 0.480931 | 0.0957637 | intron-variant | FAM63B | GRCh38.p7 | 15:58777655 | AAAAAAAGAAAATCT[A/G]TTGAATAGTTGAGCT | 54629 |
rs411007 | snp | C/G | 0.437118 | 0.165792 | intron-variant | FAM63B | GRCh38.p7 | 15:58786303 | GTTAAAAATTCTTCA[C/G]CAATTATTTTGTGTT | 54629 |
rs411211 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | FAM63B | GRCh38.p7 | 15:58834729 | TAATTCACGACTTTA[A/G]TAAGCCACTTTCATT | 54629 |
rs421829 | snp | C/G | 0.431325 | 0.172108 | intron-variant | FAM63B | GRCh38.p7 | 15:58787703 | gttgcccagggtgga[C/G]tgcagtggcgcaatc | 54629 |
rs422259 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58805409 | TAGGCTCTTTGCTTA[C/T]ATTACAACTTCTGGT | 54629 |
rs431414 | snp | C/T | 0.375797 | 0.216044 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855601 | AGTTAGAGATAATCT[C/T]TGTGTCTTATAAAAA | 54629 |
rs432978 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | FAM63B | GRCh38.p7 | 15:58785345 | AGAAGCAAATACACA[A/G]ATATTTCGACTCACT | 54629 |
rs442321 | snp | A/T | 0.0829062 | 0.185956 | utr-variant-3-prime, downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58854838 | AAATGCTGTGTGTTG[A/T]CATTCATGAAAAATA | 54629 |
rs446126 | snp | C/T | 0.430285 | 0.173197 | intron-variant | FAM63B | GRCh38.p7 | 15:58820903 | TAAGTAAGTTATATA[C/T]CTAATAAAACAAATA | 54629 |
rs449243 | snp | A/G | 0.45762 | 0.139261 | intron-variant | FAM63B | GRCh38.p7 | 15:58831041 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 54629 |
rs452698 | snp | A/G | 0.429538 | 0.173972 | intron-variant | FAM63B | GRCh38.p7 | 15:58813372 | tcatggcatgtgcct[A/G]taatcccagctactt | 54629 |
rs472200 | snp | A/C | 0.269809 | 0.249214 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860203 | AACATTTTGTTTTGT[A/C]CTTCTCTAATTTATG | 54629 |
rs474875 | snp | A/C | 0.461592 | 0.133149 | intron-variant | FAM63B | GRCh38.p7 | 15:58794504 | TCACTTTCTCCAACA[A/C]AAATCCCATAATTTT | 54629 |
rs481309 | snp | A/G | 0.451856 | 0.147493 | intron-variant | FAM63B | GRCh38.p7 | 15:58799766 | GAGCCAGACATGGAC[A/G]TGGCTTTTTGAAGGG | 54629 |
rs484952 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58781858 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 54629 |
rs499269 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58811078 | ggccccttgggccac[A/C]cctgcagtttatact | 54629 |
rs500057 | snp | A/G | 0.446771 | 0.154211 | intron-variant | FAM63B | GRCh38.p7 | 15:58822276 | CCTTTATGAATGATT[A/G]CTTCTTCTTCTTTTT | 54629 |
rs501165 | snp | G/T | 0.450859 | 0.148847 | intron-variant | FAM63B | GRCh38.p7 | 15:58811284 | ATATATCCATCACTC[G/T]AACTGTACATTTCTA | 54629 |
rs510759 | snp | A/G | 0.444931 | 0.15653 | intron-variant | FAM63B | GRCh38.p7 | 15:58782337 | ACTATTATTTAGTGC[A/G]TCCATTTTGCCTTAC | 54629 |
rs512146 | snp | G/T | 0.450609 | 0.149185 | intron-variant | FAM63B | GRCh38.p7 | 15:58807529 | CATGCCTGGCTAAAA[G/T]TTTTTTGTATTTTTT | 54629 |
rs519649 | snp | G/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58804230 | ATTGCTAAAAATGTT[G/T]AAATATCACTGTTTT | 54629 |
rs522391 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803940 | TTTTTTTTTTCAGTA[A/G]AGCTGGGGTTTCACC | 54629 |
rs523354 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803809 | TTAttttttgaggca[A/G]agtctccctctgctg | 54629 |
rs529301 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58804272 | TATTGGAAGCTGGGA[C/T]GAGATTTCATTTGAA | 54629 |
rs533831 | snp | C/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58844777 | ggagcacaccaccac[C/G]cctggctaatttttg | 54629 |
rs533904 | snp | C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58844750 | TTTGTATTTTTAGTA[C/G]AGATGGAGTTTCACC | 54629 |
rs533907 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58844748 | TGTATTTTTAGTAGA[A/G]ATGGAGTTTCACCAT | 54629 |
rs534646 | snp | A/G | 0.277778 | 0.248452 | intron-variant | FAM63B | GRCh38.p7 | 15:58844699 | gaactcctgacctca[A/G]atgatccaccgcctc | 54629 |
rs535679 | snp | A/G | 0.297128 | 0.245518 | intron-variant | FAM63B | GRCh38.p7 | 15:58843296 | CAGGTGTAGTGGTAC[A/G]TGCCTGTAGTCTCAG | 54629 |
rs546116 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58808740 | gtgggcacctgtagt[A/C]ccagctactcgggag | 54629 |
rs551943 | snp | A/T | 0.0356815 | 0.128715 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855214 | GATCATGGAGCTTAG[A/T]TTTAATTTAGATAGC | 54629 |
rs556082 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58784876 | CTGGGCTCAAGTGAT[C/G]CTTTCACTTCAGCCT | 54629 |
rs556256 | snp | C/T | 0.445724 | 0.155538 | intron-variant | FAM63B | GRCh38.p7 | 15:58802565 | GCTAAAAATGGATTT[C/T]ATATTTTTAAAGAGG | 54629 |
rs561903 | snp | C/T | 0.44638 | 0.154709 | intron-variant | FAM63B | GRCh38.p7 | 15:58783631 | TGTAATTCTTAATCA[C/T]CTAAAGAGTAAAGTA | 54629 |
rs567876 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | FAM63B | GRCh38.p7 | 15:58799432 | ATTAGCCAGGCGTGG[G/T]GGCGGGTGCCTGTAG | 54629 |
rs571030 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | FAM63B | GRCh38.p7 | 15:58851005 | gcctgggcgacagag[C/G]aagactcagtcgtga | 54629 |
rs574683 | snp | C/T | 0.448452 | 0.152042 | intron-variant | FAM63B | GRCh38.p7 | 15:58816117 | aatgCAGCATACATG[C/T]GTGCATCCATTAACT | 54629 |
rs596094 | snp | A/G | 0.44638 | 0.154709 | intron-variant | FAM63B | GRCh38.p7 | 15:58783004 | TGGGCCCAGAAGACA[A/G]AGGCTGCAGTGAGTA | 54629 |
rs597112 | snp | C/T | 0.446771 | 0.154211 | intron-variant | FAM63B | GRCh38.p7 | 15:58818486 | GGAGGACGGCTTCAG[C/T]CCAGGAATTTGAGAC | 54629 |
rs601795 | snp | C/G | 0.451732 | 0.147663 | intron-variant | FAM63B | GRCh38.p7 | 15:58797951 | CCCCTCTGAACATTG[C/G]TTTCCTCTTCTGTAA | 54629 |
rs610877 | snp | G/T | 0.461481 | 0.133325 | intron-variant | FAM63B | GRCh38.p7 | 15:58811129 | ctaaatcttggcatt[G/T]ctgtaccaataggag | 54629 |
rs618684 | snp | C/T | 0.461259 | 0.133677 | intron-variant | FAM63B | GRCh38.p7 | 15:58823723 | AAAAGAGTTGTCAGA[C/T]GAATCAATGATCAAC | 54629 |
rs620284 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58811985 | AAGTTTACAATTAAC[C/T]AATATTATTTTGAAA | 54629 |
rs624536 | snp | G/T | 0.447032 | 0.153878 | intron-variant | FAM63B | GRCh38.p7 | 15:58834299 | GATTAAGGAGTGAGA[G/T]ATtgtggggaaaaga | 54629 |
rs625312 | snp | C/T | 0.450734 | 0.149016 | intron-variant | FAM63B | GRCh38.p7 | 15:58781080 | CCTGGGCAACAAGAA[C/T]GAAACACTGTCTGGA | 54629 |
rs626228 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAM63B | GRCh38.p7 | 15:58810007 | ggcggatcacttgag[A/G]tcaggagtttgagac | 54629 |
rs633585 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58785350 | TTTTTAGAAGCAAAT[A/T]CACAGATATTTCGAC | 54629 |
rs634116 | snp | A/C | 0.00717551 | 0.0594665 | intron-variant | FAM63B | GRCh38.p7 | 15:58830646 | tagacaaaggctgtg[A/C]tgtgccttatagaga | 54629 |
rs634565 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAM63B | GRCh38.p7 | 15:58830516 | tcttttggattttgg[A/G]atgtctgcattatac | 54629 |
rs635349 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58784924 | TAACAGGCTGGGTAC[A/G]GTGGCTCACGTCTAC | 54629 |
rs637918 | snp | C/T | 0.385741 | 0.209939 | intron-variant | FAM63B | GRCh38.p7 | 15:58846071 | cattaaccatccatc[C/T]tgcctgcctccaaat | 54629 |
rs640045 | snp | C/T | 0.293551 | 0.246177 | intron-variant | FAM63B | GRCh38.p7 | 15:58852262 | CTTGCTCTATCATCC[C/T]GACTGGAGTGTAGTG | 54629 |
rs648432 | snp | C/G | 0.0970103 | 0.197722 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861645 | CCTCCCAAAGTGAAA[C/G]TTTTGAAACTGATGA | 54629 |
rs650013 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58809925 | gggcatggtggcatg[C/T]gcctgtagtcccagc | 54629 |
rs650731 | snp | A/G | 0.131038 | 0.219882 | intron-variant | FAM63B | GRCh38.p7 | 15:58773460 | GTACTGTCTTCACTT[A/G]AAACATCTCAGTGCC | 54629 |
rs652193 | snp | C/T | 0.446641 | 0.154377 | intron-variant | FAM63B | GRCh38.p7 | 15:58773115 | GAAACATTGCATCTA[C/T]AGATATAATTATCAA | 54629 |
rs654857 | snp | C/T | 0.450859 | 0.148847 | intron-variant | FAM63B | GRCh38.p7 | 15:58814545 | caaaaaattaaaaag[C/T]gagcagggtatggtg | 54629 |
rs654870 | snp | A/G | 0.457037 | 0.140127 | intron-variant | FAM63B | GRCh38.p7 | 15:58808145 | GGGGAAGCTGTGTGT[A/G]TGGGGTTAGGAGGAA | 54629 |
rs655312 | snp | A/C | 0.0879971 | 0.190408 | intron-variant | FAM63B | GRCh38.p7 | 15:58851169 | ctggccaacatggta[A/C]aaccccgtctctatt | 54629 |
rs656317 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58804229 | TTGCTAAAAATGTTT[A/G]AATATCACTGTTTTA | 54629 |
rs657649 | snp | A/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803942 | ttttttttttttcag[A/T]aaagctggggtttca | 54629 |
rs661367 | snp | C/T | 0.270351 | 0.24917 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861104 | AGGAAAAGATTCACA[C/T]GCACTAGCTTTAGGA | 54629 |
rs661852 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860961 | TGAATCTGTAACAAG[C/T]TGTCATTTATTAAGC | 54629 |
rs662149 | snp | C/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58791855 | gaccttttcttttat[C/G]tactacattccttcc | 54629 |
rs664783 | snp | C/G | 0.14665 | 0.227637 | intron-variant | FAM63B | GRCh38.p7 | 15:58808905 | tttaaagatgaaaaa[C/G]tggctgggcacggtg | 54629 |
rs664909 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58782922 | aaaaaaaaaaaaaaa[A/C]aaaaaaaaaaCAGAG | 54629 |
rs664936 | snp | C/T | 0.453331 | 0.145452 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772587 | TACTTTCTCCAATTC[C/T]TCACTTTTTTGCATA | 54629 |
rs670920 | snp | C/G | 0.39009 | 0.207062 | intron-variant | FAM63B | GRCh38.p7 | 15:58849895 | ACAAAAATTAGCCGG[C/G]TGTGGTGGCACATGC | 54629 |
rs673813 | snp | A/T | 0.470618 | 0.117591 | intron-variant | FAM63B | GRCh38.p7 | 15:58784972 | TGGCAGTCTGTCTGA[A/T]TTTCTAAATTTTAAG | 54629 |
rs677933 | snp | C/G | 0.410737 | 0.191478 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58859717 | ATGAACTAAAATTTA[C/G]ATAGATATTCAAAGT | 54629 |
rs678020 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58795977 | TTCTCCAGTATTCAA[C/T]ACCCTTTCTCCTTTC | 54629 |
rs682619 | snp | A/G | 0.476052 | 0.106772 | intron-variant | FAM63B | GRCh38.p7 | 15:58806574 | AATATTAAAACAACT[A/G]AGTTAACACCATTTG | 54629 |
rs684505 | snp | C/G | 0.448708 | 0.151707 | intron-variant | FAM63B | GRCh38.p7 | 15:58821443 | ACTTTATTTCTTAAG[C/G]TCATAAACATGTATT | 54629 |
rs688343 | snp | A/T | 0.446641 | 0.154377 | intron-variant | FAM63B | GRCh38.p7 | 15:58819867 | GGATAAGATTCTATG[A/T]ACATTGCACAAAAAA | 54629 |
rs688756 | snp | G/T | 0.402982 | 0.197728 | intron-variant | FAM63B | GRCh38.p7 | 15:58784073 | CTCGCAAATTGCTGG[G/T]ATTACAGGTGTGAGC | 54629 |
rs793571 | snp | C/T | 0.459347 | 0.136653 | intron-variant | FAM63B | GRCh38.p7 | 15:58849507 | CCAGtttttttcttt[C/T]ttgagacggagtctt | 54629 |
rs793572 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | FAM63B | GRCh38.p7 | 15:58849269 | gtgatcggcccgcct[C/T]ggcctcccaaagtgc | 54629 |
rs809904 | snp | C/T | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855830 | cgggttcaagcaatt[C/T]tcctgcctcagccct | 54629 |
rs812659 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58844584 | actgtcaacaatgca[A/G]atttttttttttttt | 54629 |
rs813219 | snp | C/T | 0.39527 | 0.203462 | intron-variant | FAM63B | GRCh38.p7 | 15:58849500 | ttttctttcttgaga[C/T]ggagtcttgctctgt | 54629 |
rs813220 | snp | A/C | 0.386884 | 0.209196 | intron-variant | FAM63B | GRCh38.p7 | 15:58844489 | tcttgggtcactgca[A/C]cctccgcctcctggg | 54629 |
rs814252 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58844557 | tttttttttttttga[A/G]acggagtctcgctct | 54629 |
rs1047390 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771652 | CCACTGTCCTTCAAG[C/T]CCAAACCCGCGGAGG | 54629 |
rs1053420 | snp | A/G | 0.496517 | 0.0415876 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861609 | AATTATTTTAAAACT[A/G]CTTAATTCTTAAAAA | 54629 |
rs1054991 | snp | A/G | 0.495407 | 0.0477027 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857201 | ATGAAATGTTCAATT[A/G]TATTAAAACAAACAA | 54629 |
rs1365452 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58816673 | TGCCTTTCCCCATTG[C/T]TCTAGAGTGCCCTAG | 54629 |
rs1551445 | snp | A/G | 0.34989 | 0.229177 | intron-variant | FAM63B | GRCh38.p7 | 15:58836359 | TTGCCACTTGTCCCC[A/G]GAATAGTTCTATGGA | 54629 |
rs1648532 | snp | C/G | 0.463018 | 0.130857 | intron-variant | FAM63B | GRCh38.p7 | 15:58784579 | AAAATGACAAATCAA[C/G]TATGACCTATTTTAG | 54629 |
rs1678977 | snp | C/T | 0.450859 | 0.148847 | intron-variant | FAM63B | GRCh38.p7 | 15:58813456 | CAGGCTGGAGAGAAG[C/T]GGCACGATCTTGGCT | 54629 |
rs1693533 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58842769 | ggagttgtgaagatt[A/T]aatgagataatccat | 54629 |
rs2002386 | snp | C/T | 0.146985 | 0.227789 | intron-variant | FAM63B | GRCh38.p7 | 15:58803834 | AAATAAGAGGCCGGG[C/T]GTGGTGGCTCACGCC | 54629 |
rs2013098 | snp | A/G | 0.350764 | 0.228794 | intron-variant | FAM63B | GRCh38.p7 | 15:58804600 | CAGGCTGGTCTCACT[A/G]CTGGGCTCAAGCAAT | 54629 |
rs2019744 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58778815 | TTCTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 54629 |
rs2054097 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58839132 | GACAAAAGATTTTAA[C/T]GCACACTCaaaaaaa | 54629 |
rs2266403 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | FAM63B | GRCh38.p7 | 15:58803817 | GGAGACTCTGCCTCA[A/G]AAAATAAGAGGCCGG | 54629 |
rs2414610 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803971 | aaaaaaaaaaaaaat[A/C]caaaaaattagccag | 54629 |
rs2414611 | snp | C/T | 0.380333 | 0.213338 | intron-variant | FAM63B | GRCh38.p7 | 15:58791622 | ACACACACACACACA[C/T]ATTTTGAGACAGGGT | 54629 |
rs2448484 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58818997 | TTTTGTTTTGTTTTA[A/G]AGACAGTGTCTTGCT | 54629 |
rs2555357 | snp | A/G | 0.431473 | 0.171952 | | | GRCh38.p7 | 15:58794916 | agttgggccgggcgc[A/G]gtggctcacggctgt | 54629 |
rs2604453 | snp | C/G | 0.430583 | 0.172886 | | | GRCh38.p7 | 15:58797313 | ggagttcaagaccag[C/G]ctgggcaacatggca | 54629 |
rs2604454 | snp | A/C | 0.45762 | 0.139261 | | | GRCh38.p7 | 15:58806533 | CTGGCCTCTTTTAAC[A/C]GTTTTATTAATCTTT | 54629 |
rs2620358 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58787437 | aaTAAATAGAATAAT[A/C]CAGTAAAGACTGGTT | 54629 |
rs2620359 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58802736 | ATTTTATTTATATTT[C/T]ACAATTAAGTTATGT | 54629 |
rs2620360 | snp | C/T | 0.473174 | 0.112665 | intron-variant | FAM63B | GRCh38.p7 | 15:58808638 | GAGACAGAGTCTCGC[C/T]CTGTCGCCCAGGCTG | 54629 |
rs3985718 | in-del | -/AC | | | intron-variant | FAM63B | GRCh38.p7 | 15:58794358 | TATTTTATTCTTAAA[-/AC]ACACACACACACACA | 54629 |
rs3985719 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58790586 | TGTCTTACCCCCCAC[C/T]AAGGTCTATTGTCAA | 54629 |
rs4145842 | snp | C/G/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58801474 | AGTTAATACATAATT[C/G/T]gaaagataatacgta | 54629 |
rs4566091 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | FAM63B | GRCh38.p7 | 15:58836416 | AAAGACCATGCATTG[C/T]ATTTGATAGAGTAAC | 54629 |
rs4774311 | snp | C/T | 0.4087 | 0.193169 | intron-variant | FAM63B | GRCh38.p7 | 15:58779382 | GTTTTTGCTCTATTT[C/T]TCCCTACCTCCTTGA | 54629 |
rs4774312 | snp | A/G | 0.49941 | 0.0171624 | intron-variant | FAM63B | GRCh38.p7 | 15:58848725 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 54629 |
rs4775094 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | FAM63B | GRCh38.p7 | 15:58823796 | GAAGCAATAAAAACT[A/G]TTACAAAAGTATATT | 54629 |
rs4775095 | snp | C/T | 0.44638 | 0.154709 | intron-variant | FAM63B | GRCh38.p7 | 15:58828427 | ATCAAGTTTCCTTCC[C/T]TCCTATTTCTACTTT | 54629 |
rs4775096 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | FAM63B | GRCh38.p7 | 15:58848130 | CCATAAGTGGGCAGT[C/T]TTGGAGCCACAGGTC | 54629 |
rs4775097 | snp | C/T | 0.495745 | 0.0459295 | intron-variant | FAM63B | GRCh38.p7 | 15:58848602 | TAAAAATCAATTATC[C/T]GGGCATGGTGGCGGG | 54629 |
rs5812950 | in-del | -/A | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58773136 | CCTAGGAAAAAAAAA[-/A]CAAAACAAACTGGGT | 54629 |
rs5812951 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58787737 | GCGAGAGTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs6494041 | snp | A/G | 0.302435 | 0.244439 | intron-variant | FAM63B | GRCh38.p7 | 15:58846907 | GATTGGACTAGTCAT[A/G]TAGGCTTAATTGGAA | 54629 |
rs6494042 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | FAM63B | GRCh38.p7 | 15:58849787 | cactctgtcaccaag[A/G]ctagagtacagtggt | 54629 |
rs7162584 | snp | G/T | 0.0626037 | 0.165477 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58858811 | GAGGCATTACAAATA[G/T]TCTACAGTTTGTATT | 54629 |
rs7162921 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAM63B | GRCh38.p7 | 15:58779866 | CCCCTTGGTATGAGT[A/G]GTCTTTTAGTTAAAA | 54629 |
rs7163754 | snp | C/G | 0.0685596 | 0.171987 | intron-variant | FAM63B | GRCh38.p7 | 15:58853438 | CCTACCATGTTATGT[C/G]TAGGTTTTCACTCAA | 54629 |
rs7164053 | snp | A/G | 0.4087 | 0.193169 | intron-variant | FAM63B | GRCh38.p7 | 15:58780180 | GAGGCCGAGGCAGGC[A/G]GATCACTTGATGTCA | 54629 |
rs7164683 | snp | A/G | 0.499053 | 0.0217445 | intron-variant | FAM63B | GRCh38.p7 | 15:58854173 | CTCTTGAACCCAGGA[A/G]GTGGAGGTTGCAGTG | 54629 |
rs7164844 | snp | C/T | 0.409041 | 0.192888 | intron-variant | FAM63B | GRCh38.p7 | 15:58780002 | ACTCAGTTATTTTTG[C/T]GTCCAGATACTGTGC | 54629 |
rs7165019 | snp | C/T | 0.350764 | 0.228794 | intron-variant | FAM63B | GRCh38.p7 | 15:58780098 | TGTAGACTATTGTTC[C/T]TATTTTATATATATA | 54629 |
rs7168421 | snp | A/C | 0.138886 | 0.22395 | intron-variant | FAM63B | GRCh38.p7 | 15:58801928 | CAGCCAGATGCCAAA[A/C]TTCTTTTTTTTACTT | 54629 |
rs7168825 | snp | C/G | 0.350764 | 0.228794 | intron-variant | FAM63B | GRCh38.p7 | 15:58780329 | GAATCACTTTAACCT[C/G]GGAGGGAGGTTGCGG | 54629 |
rs7169205 | snp | A/G | 0.316492 | 0.240995 | intron-variant | FAM63B | GRCh38.p7 | 15:58788004 | ATCTCTTTCAAAACA[A/G]AAGTTTTCAAAGCTA | 54629 |
rs7169796 | snp | C/T | 0.350764 | 0.228794 | intron-variant | FAM63B | GRCh38.p7 | 15:58780292 | GCCTGTAATCCCAGC[C/T]ACTCGGGAGGCTGAG | 54629 |
rs7170538 | snp | A/C | 0.403334 | 0.197456 | intron-variant | FAM63B | GRCh38.p7 | 15:58775488 | CATGAAGAAAGTGGT[A/C]TTTTACTTTGATATT | 54629 |
rs7171198 | snp | C/G | 0.403334 | 0.197456 | intron-variant | FAM63B | GRCh38.p7 | 15:58775661 | GTGAAGACAGTAACA[C/G]CATTTTTCAAACCTG | 54629 |
rs7171482 | snp | G/T | 0.410905 | 0.191336 | intron-variant | FAM63B | GRCh38.p7 | 15:58814296 | ttgatgtgcttgttt[G/T]ccatttgcatattct | 54629 |
rs7172793 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58785161 | AAAAAAAAAAAAAGA[A/G]AAGCAAGCTTTTGGG | 54629 |
rs7173746 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58834145 | ttgacacagcacacg[A/T]ttcagggagcacagg | 54629 |
rs7174187 | snp | C/T | 0.409382 | 0.192607 | intron-variant | FAM63B | GRCh38.p7 | 15:58837538 | TGAGCCATGATGGCA[C/T]CAAAAAAAAAAAAAA | 54629 |
rs7178522 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | FAM63B | GRCh38.p7 | 15:58843585 | TCGTAAATTAATTCT[A/G]CATGGAGTAGTTACT | 54629 |
rs7178955 | snp | A/G | 0.496746 | 0.040204 | intron-variant | FAM63B | GRCh38.p7 | 15:58843561 | AACCTATTCTGTCCA[A/G]AAATACCCTCGTAAA | 54629 |
rs7178970 | snp | C/T | 0.4087 | 0.193169 | intron-variant | FAM63B | GRCh38.p7 | 15:58778719 | ATAGCCTCGACCTCC[C/T]GAGCTCAAGCAATCC | 54629 |
rs7179154 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58778802 | cACCTAATTTTTTTT[C/T]TTTTTTTCttttttt | 54629 |
rs7179158 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58778810 | TTTTTTTCTTTTTTT[C/T]ttttttttttttttt | 54629 |
rs7180055 | snp | C/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58852698 | taaaatagaagaact[C/T]ttaagtttgttgtga | 54629 |
rs7180252 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58852844 | TTTAATGGTGGGATT[C/G/T]TACATGTTAAATCTC | 54629 |
rs7180472 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58778801 | ccACCTAATTTTTTT[C/T]CTTTTTTTCtttttt | 54629 |
rs7181446 | snp | A/G | 0.122064 | 0.214785 | intron-variant | FAM63B | GRCh38.p7 | 15:58840380 | AAATTCTGGAAAAAT[A/G]CCTCTGTGTTTCTTT | 54629 |
rs7181998 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | FAM63B | GRCh38.p7 | 15:58840584 | TACAATTAAACTGGG[C/T]GGATCCTCTTTGTGA | 54629 |
rs7182559 | snp | A/G | 0.444444 | 0.157135 | intron-variant | FAM63B | GRCh38.p7 | 15:58791662 | tgtgtgtgtgtgtgt[A/G]tgtgtgtgtgtgtaa | 54629 |
rs7183811 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | FAM63B | GRCh38.p7 | 15:58816459 | tctgttgcccagact[A/G]gagtgcagtagtgtg | 54629 |
rs7183900 | snp | C/T | 0.41023 | 0.191902 | intron-variant | FAM63B | GRCh38.p7 | 15:58800704 | CCAGGTGTGGTGGTG[C/T]GTGTCTTTAGTCCCA | 54629 |
rs7183956 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAM63B | GRCh38.p7 | 15:58816433 | tttgtttttttgaga[C/T]aagatcttgctctgt | 54629 |
rs7494967 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58823255 | ccattctccttcctc[A/G]gcctcctgagtagct | 54629 |
rs8024172 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | FAM63B | GRCh38.p7 | 15:58828837 | tgggattacaggcat[A/G]agccactgcgcccag | 54629 |
rs8025383 | snp | C/T | 0.33693 | 0.2344 | intron-variant | FAM63B | GRCh38.p7 | 15:58774477 | CAACAAGAGTGAAAC[C/T]CCGTCCCAAAAAAAG | 54629 |
rs8029301 | snp | C/T | 0.374 | 0.217081 | intron-variant | FAM63B | GRCh38.p7 | 15:58829637 | AGGGGCTTTTAAAAA[C/T]ATCTTTCTGAAGGGA | 54629 |
rs8029869 | snp | A/C/G | 0.033613 | 0.125208 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772079 | GGAGGAGACCGCTCA[A/C/G]GTGCTGGCGGCCTCC | 54629 |
rs8030897 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | FAM63B | GRCh38.p7 | 15:58839064 | TTTCTATAGGAATTT[A/G]CTAAACCCTATATAT | 54629 |
rs8031032 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FAM63B | GRCh38.p7 | 15:58839022 | CCTAGGAAGGGTCAC[C/T]TCCAGTTTCTTTACT | 54629 |
rs8032298 | snp | G/T | 0.44638 | 0.154709 | intron-variant | FAM63B | GRCh38.p7 | 15:58784302 | CTGCGATCCAGCCTG[G/T]AGGACAGTGAGAACA | 54629 |
rs8033478 | snp | G/T | 0.421051 | 0.182323 | intron-variant | FAM63B | GRCh38.p7 | 15:58784412 | CTAGATAATAAAAAT[G/T]TATTTGGCCTCTATT | 54629 |
rs8038226 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770023 | agcaaaaacaaaaAC[A/C]AAAAAACATATAAGT | 54629 |
rs8038358 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770030 | acaaaaACAAAAAAA[A/C]ATATAAGTATGTATT | 54629 |
rs8039141 | snp | A/G | 0.304937 | 0.243889 | intron-variant | FAM63B | GRCh38.p7 | 15:58843711 | TGGTGGTGGGCACCT[A/G]TAGTCCCAGCTACTC | 54629 |
rs8039747 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58843520 | TGCTTTCCTCCATAT[C/T]GGATCACAAAAGAAC | 54629 |
rs9646204 | snp | A/G | 0.32885 | 0.23724 | intron-variant | FAM63B | GRCh38.p7 | 15:58778230 | AGAAGATAGAGTATT[A/G]CAATATCTAGTCATT | 54629 |
rs9672161 | snp | C/T | 0 | 0 | downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58862206 | tcatgtcactgcagt[C/T]tagcctgagcaacag | 54629 |
rs9744045 | snp | C/G | 0.408871 | 0.193029 | intron-variant | FAM63B | GRCh38.p7 | 15:58782644 | ATAAGATTTCATTGA[C/G]TGGAAAGTGTTCTGC | 54629 |
rs9788674 | snp | A/T | 0.412583 | 0.189912 | intron-variant | FAM63B | GRCh38.p7 | 15:58805081 | GATTCTTGAAGGGAA[A/T]TTGGAATATTGGCTC | 54629 |
rs9788774 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FAM63B | GRCh38.p7 | 15:58803340 | GGGCATGGTGATGCG[C/T]GCCTGTAGTCCCAGC | 54629 |
rs10563818 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58853842 | AAAAAAAAAAAAAAA[-/A]GTCTGTTTATTATGG | 54629 |
rs10699783 | in-del | -/CT | 0.448323 | 0.15221 | intron-variant | FAM63B | GRCh38.p7 | 15:58824792 | TCCTGCCTCAGCCTC[-/CT]CTGAGTAGCTGGGAC | 54629 |
rs10718322 | in-del | -/T | 0.446249 | 0.154875 | intron-variant | FAM63B | GRCh38.p7 | 15:58779063 | CACTGTGCCCAACCA[-/T]TTTTTTTTTTTTCTC | 54629 |
rs10719398 | in-del | -/T | 0.499996 | 0.00139776 | intron-variant | FAM63B | GRCh38.p7 | 15:58848078 | ATGAGACAGATGAGA[-/T]TTTTTTTTTTTTTTT | 54629 |
rs10851640 | snp | C/T | 0.497855 | 0.0326773 | intron-variant | FAM63B | GRCh38.p7 | 15:58845671 | aaagtagagctgtta[C/T]acaatccggcaatcc | 54629 |
rs11071397 | snp | C/G | 0.348134 | 0.229934 | intron-variant | FAM63B | GRCh38.p7 | 15:58815298 | CCTTAAAAGCATCCA[C/G]TTTAATTAAAATAAG | 54629 |
rs11071398 | snp | A/G | 0.425123 | 0.178415 | intron-variant | FAM63B | GRCh38.p7 | 15:58827878 | TCCTCATCTTTACTT[A/G]AGCACTTATTTTTTG | 54629 |
rs11071399 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | FAM63B | GRCh38.p7 | 15:58847056 | TCATACATTAGCTGA[A/G]CATGCCAAGAGCTCT | 54629 |
rs11299168 | in-del | -/A | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58787754 | AAAAAAAAAAAAAAA[-/A]GCCTGGCTATAAAGA | 54629 |
rs11335033 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58846596 | AAAGTGAGACTCCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs11369418 | in-del | -/A | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855091 | AGGGATTCAAAAAAA[-/A]CAAAAACAAAAGAAT | 54629 |
rs11385535 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58774493 | CGTCCCAAAAAAAGA[-/A]AAAAAAAAAAAAAAA | 54629 |
rs11399455 | in-del | -/T | 0.411074 | 0.191194 | intron-variant | FAM63B | GRCh38.p7 | 15:58840193 | GTCACAATGGATGTG[-/T]TAATCAAACTGATCC | 54629 |
rs11463341 | in-del | -/A | 0.384401 | 0.210799 | intron-variant | FAM63B | GRCh38.p7 | 15:58802105 | GGAAGTAAAAAGTTC[-/A]AAAGCACTATAGTAT | 54629 |
rs11543227 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861282 | TCAATTTGCTGTGAC[A/G]TATCAAAGATCTCTT | 54629 |
rs11629654 | snp | C/T | 0.464841 | 0.127841 | intron-variant | FAM63B | GRCh38.p7 | 15:58826368 | ccaagtagctgggat[C/T]acaggcatgcgccac | 54629 |
rs11629739 | snp | C/T | 0.244776 | 0.249945 | intron-variant | FAM63B | GRCh38.p7 | 15:58819380 | TTGAGCCTGGGAGGT[C/T]GAGGCTGCAGTGGGC | 54629 |
rs11629758 | snp | C/G | 0 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856622 | TTAGTAAAATAACCA[C/G]ATATACTACAGAACT | 54629 |
rs11630503 | snp | C/T | 0.147991 | 0.228242 | intron-variant | FAM63B | GRCh38.p7 | 15:58774340 | ATACAAAAAATTAGA[C/T]GGGCATGGTGGTGGG | 54629 |
rs11631244 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | FAM63B | GRCh38.p7 | 15:58813911 | gtagcaatatttcat[G/T]gtagttttaacttgc | 54629 |
rs11631334 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | FAM63B | GRCh38.p7 | 15:58784001 | GTAGCTATTTTCTTT[A/T]ATTAATTTAAATATT | 54629 |
rs11631799 | snp | A/G | 0.410737 | 0.191478 | intron-variant | FAM63B | GRCh38.p7 | 15:58838728 | AGTAGTTGGGATTAC[A/G]GGCGGGTACCACCAC | 54629 |
rs11631838 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58838677 | ccacaacctccacct[C/T]tcaggttcaagcgat | 54629 |
rs11634452 | snp | A/G | 0.152001 | 0.229992 | intron-variant | FAM63B | GRCh38.p7 | 15:58812726 | agctaggcatgatgg[A/G]acatgcctgtagtcc | 54629 |
rs11635016 | snp | C/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58828374 | AATTTGAACACAAAT[C/T]TGAGACAGGACCACA | 54629 |
rs11635746 | snp | A/T | 0.444444 | 0.157135 | intron-variant | FAM63B | GRCh38.p7 | 15:58804253 | TTAGCAATAGAAACC[A/T]CTTTTCAAATGAAAT | 54629 |
rs11638653 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAM63B | GRCh38.p7 | 15:58819202 | gcctgtgatcccaac[A/G]ttttgaaagaccaag | 54629 |
rs11639208 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAM63B | GRCh38.p7 | 15:58773425 | AAAATTAGAAACCTT[A/G]CCATTGTCTGGTGCA | 54629 |
rs11852332 | snp | C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58826290 | gctggagtacaatgg[C/G]gcaaccttggcttac | 54629 |
rs11857460 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58777335 | TTAGAAAATCAATAG[A/C]CTGAACAAACCGGGA | 54629 |
rs11858548 | snp | C/T | 0.120326 | 0.21374 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769525 | ATGTATTATATGTAA[C/T]ACATATTATGTGTgg | 54629 |
rs12324310 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58776520 | TAATAAAAATGTAGT[A/C]CATTACTATTGTCAA | 54629 |
rs12437928 | snp | C/T | 0.446771 | 0.154211 | intron-variant | FAM63B | GRCh38.p7 | 15:58835820 | aaaagaaagtcagtg[C/T]ccctgaaacatagca | 54629 |
rs12438114 | snp | A/G | 0.380333 | 0.213338 | intron-variant | FAM63B | GRCh38.p7 | 15:58797265 | ttatcccagcacttc[A/G]cgagactgaggcagg | 54629 |
rs12439632 | snp | C/G | 0.349671 | 0.229272 | intron-variant | FAM63B | GRCh38.p7 | 15:58811764 | ATTCCAGTTGCTGCA[C/G]TCCATAGAGGTTAGT | 54629 |
rs12591310 | snp | A/G | 0.34659 | 0.230587 | intron-variant | FAM63B | GRCh38.p7 | 15:58792069 | tactaaaaattgact[A/G]ttgatttagccataa | 54629 |
rs12593426 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58812612 | tgcctgtaatcctag[A/G/T]actttgggaggccaa | 54629 |
rs12594276 | snp | G/T | 0.446902 | 0.154045 | intron-variant | FAM63B | GRCh38.p7 | 15:58832806 | GCTGGGATTACAGGC[G/T]TGAGCCACCGTGTGC | 54629 |
rs12595057 | snp | A/G | 0.34659 | 0.230587 | intron-variant | FAM63B | GRCh38.p7 | 15:58830627 | ctatctagcacatgt[A/G]ttttctctataaggc | 54629 |
rs12899744 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58782910 | TTAATTTTTTCTCTC[C/T]Gtttttttttttttt | 54629 |
rs12899746 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58782912 | AATTTTTTCTCTCTG[G/T]ttttttttttttttt | 54629 |
rs12900320 | snp | A/G | 0.445855 | 0.155373 | intron-variant | FAM63B | GRCh38.p7 | 15:58800911 | CTCTCACAAAAAATC[A/G]GTTAACTAGTTGTCT | 54629 |
rs12901111 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58829046 | GGATTATTTGAATCA[A/G]TAACACCTCTTTGAG | 54629 |
rs12901309 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58844875 | agccaagatcacacc[A/C]ctgcactccagcctg | 54629 |
rs12901817 | snp | C/T | 0.446641 | 0.154377 | intron-variant | FAM63B | GRCh38.p7 | 15:58801098 | CCTGCCTCAGCCTCC[C/T]GAGTAGTTGGGACTA | 54629 |
rs12905507 | snp | A/G | 0.290201 | 0.246747 | intron-variant | FAM63B | GRCh38.p7 | 15:58829414 | TGTCTTCCCTTTGCC[A/G]TAACTAGTTTGATGT | 54629 |
rs12914164 | snp | A/G | 0.44651 | 0.154543 | intron-variant | FAM63B | GRCh38.p7 | 15:58834698 | TCTTTCCATGTAAAT[A/G]TGTCATTTTTTTCTA | 54629 |
rs12915713 | snp | A/T | 0.371582 | 0.218444 | intron-variant | FAM63B | GRCh38.p7 | 15:58815663 | CAAGAAGAAAGGATA[A/T]TATTTCCTTCttttt | 54629 |
rs16940766 | snp | A/T | 0.121369 | 0.214369 | upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770938 | GCGCTAAAGGGTCAC[A/T]GCCAAGCTGTCCGCC | 54629 |
rs16940768 | snp | A/T | 0.121717 | 0.214577 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771307 | GCGCCAGGGCGCTGT[A/T]GCTGCCAATACAGCT | 54629 |
rs16940771 | snp | A/G | 0.122064 | 0.214785 | intron-variant | FAM63B | GRCh38.p7 | 15:58774136 | ATTCAATTCAGACAG[A/G]TTCAAGTGAATGATC | 54629 |
rs16940795 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | FAM63B | GRCh38.p7 | 15:58807750 | AATCTGACAAACAAG[C/T]CTTTGTGATCCAGCC | 54629 |
rs16940810 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | FAM63B | GRCh38.p7 | 15:58822960 | AAGAATTAAAACTAA[C/T]GACTACAGGAGCATA | 54629 |
rs16940850 | snp | A/G | 0.482053 | 0.093012 | intron-variant | FAM63B | GRCh38.p7 | 15:58852000 | GTCTTAAATGTGATG[A/G]TCATGGCTGGGTGTA | 54629 |
rs16940856 | snp | A/G | 0.16976 | 0.236773 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855349 | TTTTGAGGAATTTTG[A/G]AGTCTTTATCATAGG | 54629 |
rs16940866 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861301 | CAAAGATCTCTTTGT[A/G]CCAGGCCAAGACTGG | 54629 |
rs17190720 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | FAM63B | GRCh38.p7 | 15:58777171 | GTTTTTGGTCTTTCC[C/G]TAGTTCGCTTATGTC | 54629 |
rs17190727 | snp | A/C | 0.463234 | 0.130503 | intron-variant | FAM63B | GRCh38.p7 | 15:58781591 | CTTGTGGGTTGTCTC[A/C]TAAAATTTTCCTGTT | 54629 |
rs17236229 | snp | A/G | 0.0517044 | 0.152246 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772910 | GAATGTGTTAAGGGA[A/G]CTAAAACTCTAAAGA | 54629 |
rs17236243 | snp | A/G | 0.328382 | 0.237395 | intron-variant | FAM63B | GRCh38.p7 | 15:58775605 | GATGAGGATAATGTA[A/G]CGTTCCCAATGATGA | 54629 |
rs17269439 | snp | A/C | 0.0352966 | 0.128072 | upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770945 | AGGGTCACAGCCAAG[A/C]TGTCCGCCTCCTGCC | 54629 |
rs17301982 | snp | G/T | 0.188631 | 0.242351 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772766 | TAAGGAAAAGCATTG[G/T]TCTGAGACCCAATTA | 54629 |
rs28380111 | snp | G/T | 0.375 | 0.216506 | intron-variant | FAM63B | GRCh38.p7 | 15:58852944 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 54629 |
rs28394222 | snp | C/T | 0.353803 | 0.227431 | intron-variant | FAM63B | GRCh38.p7 | 15:58804958 | GATATAGTAAGACTC[C/T]ATCTCAAAAAATTAG | 54629 |
rs28404302 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840844 | TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGAGATG | 54629 |
rs28412567 | snp | A/T | 0.347473 | 0.230215 | intron-variant | FAM63B | GRCh38.p7 | 15:58810014 | ACTCCTGACCTCAAG[A/T]GATCCGCCCACCTCA | 54629 |
rs28433983 | snp | G/T | 0.375 | 0.216506 | intron-variant | FAM63B | GRCh38.p7 | 15:58852936 | TGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 54629 |
rs28470867 | snp | C/T | 0.346368 | 0.23068 | intron-variant | FAM63B | GRCh38.p7 | 15:58792434 | AACATGGTAAAACCC[C/T]GTCTCTACTAAGAAC | 54629 |
rs28502045 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58854923 | TCATAACTCATATCA[C/G]TTAGTAAGCTATTAT | 54629 |
rs28510910 | snp | A/G | 0.346147 | 0.230772 | intron-variant | FAM63B | GRCh38.p7 | 15:58790188 | AGATGTCTGCAAATC[A/G]CCTTAAAAAGAAAAT | 54629 |
rs28533385 | snp | A/G | 0.447032 | 0.153878 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769882 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 54629 |
rs28537903 | snp | C/T | 0.41408 | 0.188621 | intron-variant | FAM63B | GRCh38.p7 | 15:58810080 | CCAACTAGCTTCTGA[C/T]ACATAGTAGATACTC | 54629 |
rs28541765 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58816890 | GCCAGGAGTTTGAGG[C/T]TGCAGTGCACTATGA | 54629 |
rs28549775 | snp | A/C | 0.447162 | 0.153712 | intron-variant | FAM63B | GRCh38.p7 | 15:58829358 | TACTCATCTGCAATA[A/C]ATTTTAAAATTTAAT | 54629 |
rs28559610 | snp | A/G | 0.0021042 | 0.0323678 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771815 | CGCCGGCACCTGCCA[A/G]GCAGAACTGACCGCC | 54629 |
rs28580321 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58797580 | GCTGCTAGAAAATTT[A/T]AAATTACATTTGAGC | 54629 |
rs28582933 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58827883 | ATCTTTACTTAAGCA[A/C]TTATTTTTTGGCACA | 54629 |
rs28599729 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840985 | TTTTTTTTTTTTTTT[A/T]ATTTTTTTTGGTGTG | 54629 |
rs28613590 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58817735 | TCAAAAAACAAAAAT[A/T]AAAAAATAAAAGTTT | 54629 |
rs28617688 | snp | C/T | 0.414741 | 0.188044 | intron-variant | FAM63B | GRCh38.p7 | 15:58790264 | TTTTAAGTTTTTTTT[C/T]CCCCATGGGACTCTA | 54629 |
rs28625305 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58777793 | GTATTTTTCCTTTTT[A/G]TTGTTTTTTTATGGA | 54629 |
rs28649816 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58773437 | CTTGCCATTGTCTGG[C/T]GCATAATGGCACTGA | 54629 |
rs28676714 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857455 | AGGAGAATCGCTTGA[A/G]CCCAGGAGGCAGTGA | 54629 |
rs28683473 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58850166 | TAAAGTGGATATTAA[G/T]TTAATGCTTGACCAA | 54629 |
rs28689473 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58839844 | CTTTTTTTTTTTTTT[C/T]CTTTTTGGGACAGAG | 54629 |
rs28701980 | snp | G/T | 0.336245 | 0.234652 | intron-variant | FAM63B | GRCh38.p7 | 15:58791175 | ACAGAGTGAGACTCC[G/T]TCTCAAAAAAAAAAA | 54629 |
rs28711432 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840842 | TTTTTTTTTTTTTTT[G/T]TATTTTTAGTAGAGA | 54629 |
rs28721510 | snp | G/T | 0.48 | 0.0979796 | intron-variant | FAM63B | GRCh38.p7 | 15:58839322 | TAAGTTAGACTGTTT[G/T]TTTGTTTGTTTGTTT | 54629 |
rs28733370 | snp | C/G | 0.350764 | 0.228794 | intron-variant | FAM63B | GRCh38.p7 | 15:58779385 | TTTGCTCTATTTCTC[C/G]CTACCTCCTTGATGA | 54629 |
rs28734829 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAM63B | GRCh38.p7 | 15:58792293 | CAAGAGAAGTGAAAA[C/T]GTATGTCCATACAGC | 54629 |
rs28736366 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58788029 | AAGCTAGTTGATTAC[C/G]CAGTCTCACCTTTCT | 54629 |
rs28748572 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58839396 | GAGTGCAGTGGCACA[A/G]TCTTGGCTCACTGCA | 54629 |
rs28793354 | snp | A/G | 0.346368 | 0.23068 | intron-variant | FAM63B | GRCh38.p7 | 15:58792647 | AGCAGTATTATTCAT[A/G]GTAGTCAAAAAATGG | 54629 |
rs28800895 | snp | C/T | 0.375797 | 0.216044 | intron-variant | FAM63B | GRCh38.p7 | 15:58792837 | TAGTGTATGATTCCA[C/T]CTATATGAAACATCC | 54629 |
rs28812884 | snp | A/G | 0.452227 | 0.146984 | intron-variant | FAM63B | GRCh38.p7 | 15:58808498 | CTTGTTTTCTTTACT[A/G]CTACGCATTTAAGTT | 54629 |
rs28876251 | snp | C/T | 0.347032 | 0.230401 | intron-variant | FAM63B | GRCh38.p7 | 15:58819121 | AGCTGGGACTATGGA[C/T]GTGCACCACCATGTC | 54629 |
rs28889637 | snp | A/G | 0.347473 | 0.230215 | intron-variant | FAM63B | GRCh38.p7 | 15:58817580 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTGGGT | 54629 |
rs33978454 | in-del | -/T/TT | 0.499971 | 0.00379382 | intron-variant | FAM63B | GRCh38.p7 | 15:58798458 | TGCAGTAAAAAAAAA[-/T/TT]TTTTTTTTTTTTTTT | 54629 |
rs34021117 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58837300 | ATAGAGGCTGGGCAT[-/G]GGTGGCTCATGTGTG | 54629 |
rs34082956 | in-del | -/A | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803969 | ACCCCAGCTCTACTG[-/A]AAAAAAAAAAAAAAA | 54629 |
rs34152133 | in-del | -/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58777349 | ACTGAACAAACCGGG[-/C]AGGATTTGAGCAAAG | 54629 |
rs34161206 | in-del | -/AA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58846093 | TGGTTAATGGATGTT[-/AA]AAAAAAAAAAAAAAA | 54629 |
rs34168648 | in-del | -/T | | | intron-variant, downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58832229 | TTTTTTTTTTTTTTT[-/T]GAAATGGAATTTCGC | 54629 |
rs34186551 | in-del | -/T | 0.448452 | 0.152042 | intron-variant | FAM63B | GRCh38.p7 | 15:58805771 | GTTTATCAGTTGTTG[-/T]TTTTTTATTAAGACA | 54629 |
rs34282928 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58783660 | AGAATGGTCCGGGCA[-/T]TGGTGGCTTACACCC | 54629 |
rs34289953 | in-del | -/C | 0.337841 | 0.23406 | intron-variant | FAM63B | GRCh38.p7 | 15:58794999 | GAGACCACGGTGAAA[-/C]CCCGTCTCTACTAAA | 54629 |
rs34347740 | in-del | -/A | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58799579 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs34362744 | snp | A/G | 0.44651 | 0.154543 | intron-variant | FAM63B | GRCh38.p7 | 15:58820271 | TTCCATCTCAAAACA[A/G]ACAAACAAACAAACA | 54629 |
rs34432832 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58811096 | GCCCAAGGGGCCCAC[-/A]AATAAATAACACAGT | 54629 |
rs34452582 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58783885 | GGGGAGGTTGAGGGT[A/C]CAATGAGCCATGATT | 54629 |
rs34518608 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58794644 | GGGGAGAGAATGACA[-/G]GGAGCAAGTGGATAC | 54629 |
rs34546804 | snp | G/T | 0.299916 | 0.244966 | intron-variant | FAM63B | GRCh38.p7 | 15:58798804 | GCTAGTTATTTGGAG[G/T]TGTCAACATGTAGTT | 54629 |
rs34575283 | in-del | -/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58824791 | CTCCTGCCTCAGCCT[-/C]CCTGAGTAGCTGGGA | 54629 |
rs34592774 | in-del | -/AA | 0.475437 | 0.108066 | intron-variant | FAM63B | GRCh38.p7 | 15:58844560 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 54629 |
rs34605445 | in-del | -/A | 0.408359 | 0.193449 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860967 | AAATGACAGCTTGTT[-/A]ACAGATTCACACATT | 54629 |
rs34657462 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58815693 | TCTTTTTTCTTTTTC[C/T]TTTTTTTTGGACAGA | 54629 |
rs34660898 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58817448 | TGATGGTATTACGTT[-/G]GGCGCAGTGGCTCAC | 54629 |
rs34666834 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58826226 | TGTATTCACACAATC[-/T]TTTTTTTTTTTTTTT | 54629 |
rs34747262 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58814795 | TTCTTTAATTTTAAC[-/T]TTTTTTTTTTTTTTT | 54629 |
rs34778747 | in-del | -/C | | | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769395 | GCCACTGTACTATAG[-/C]CCTGGGTGACAAAGC | 54629 |
rs34781375 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58817941 | AGGATAAACGTCCTA[G/T]AATTTTTCACAGCAG | 54629 |
rs34805327 | snp | A/G | 0.00207676 | 0.0321569 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771749 | GACAGCCGTGGCCGG[A/G]GTGGGTCATGAGTTG | 54629 |
rs34849581 | snp | C/T | 0.438246 | 0.16451 | intron-variant | FAM63B | GRCh38.p7 | 15:58831039 | ATATATATATATACA[C/T]ACACACACACACACA | 54629 |
rs34880782 | snp | A/G | 0.453453 | 0.145282 | intron-variant | FAM63B | GRCh38.p7 | 15:58793323 | CGGGTGTGGTGGCAC[A/G]TGCCTGTAGTCCCAG | 54629 |
rs34909401 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58837969 | GTAAGACCTTCTTTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs34999651 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58843833 | TGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 54629 |
rs35046523 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58796179 | TGGGTAAGGAGTAGG[-/A]AAAGGCTTAATGGAG | 54629 |
rs35059967 | snp | C/G | 0.213399 | 0.256233 | intron-variant | FAM63B | GRCh38.p7 | 15:58854048 | AGGAGTGTGAGACCA[C/G]CCTGGCCAACATAGT | 54629 |
rs35110462 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58830843 | TGTTTGACCTCAGCT[-/G]GGGAATGTGCACATT | 54629 |
rs35205720 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58843832 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs35213947 | in-del | -/T | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58858535 | ATAATTGTTCATATA[-/T]TTAATGTTCACATGT | 54629 |
rs35322298 | snp | A/C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58774585 | ATGACAGACATATAA[A/C/G]CAATAATTACAGTGC | 54629 |
rs35327191 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58775498 | TGGTCTTTTACTTTG[-/A]ATATTAGGCTAGAAG | 54629 |
rs35354059 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58845910 | AACATGGATGGAACT[-/G]GGAGGTCATAATGTT | 54629 |
rs35379834 | in-del | -/A | 0.375 | 0.216506 | intron-variant | FAM63B | GRCh38.p7 | 15:58844943 | ACTGAGACCCTGCCT[-/A]AAAAAAAAAAAAAAA | 54629 |
rs35531909 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58828249 | CCCATCCTTTTGAGG[-/A]AAAAATACATTAATG | 54629 |
rs35536174 | snp | C/T | 0.14665 | 0.227637 | intron-variant | FAM63B | GRCh38.p7 | 15:58850016 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 54629 |
rs35589397 | in-del | -/TA | 0.0912534 | 0.193131 | intron-variant | FAM63B | GRCh38.p7 | 15:58816669 | AGAACTAGGGCACTC[-/TA]GAGCAATGGGGAAAG | 54629 |
rs35669038 | in-del | -/TTG | 0.0498117 | 0.149749 | intron-variant | FAM63B | GRCh38.p7 | 15:58841440 | GACAGAGTTTCACTC[-/TTG]TTGCCCTTCCTGGAG | 54629 |
rs35710937 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58778794 | ACCATGCCCACCTAA[A/T]TTTTTTTCTTTTTTT | 54629 |
rs35724367 | in-del | -/T | 0.479663 | 0.0987666 | intron-variant | FAM63B | GRCh38.p7 | 15:58840841 | ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 54629 |
rs35764277 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58791192 | CTCAAAAAAAAAAAA[-/A]GGGAGCCATCAGGAA | 54629 |
rs35765377 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58850797 | TTGCCATGTTGCTCA[A/G]GCTGGTCTCAAACTC | 54629 |
rs35800859 | in-del | -/T | 0.445855 | 0.155373 | intron-variant | FAM63B | GRCh38.p7 | 15:58813747 | TGTATTTTTTTTTTT[-/T]AAGAAAGCGACAAAC | 54629 |
rs35815178 | in-del | -/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852004 | AAATGTGATGATCAT[-/G]GGCTGGGTGTAGTGG | 54629 |
rs36008859 | in-del | -/T | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855182 | ATTTAGGAATGTACA[-/T]TTTTAGGTATTATCT | 54629 |
rs36028781 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58812214 | AGGCCGAGGCGGGTG[A/G]ATCATGAAGTCAGGA | 54629 |
rs36037356 | in-del | -/A | | | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769989 | GAGAGACTCCGTTTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs55897928 | in-del | -/C | 0.298144 | 0.245321 | intron-variant | FAM63B | GRCh38.p7 | 15:58853030 | CAGTCTCGCTCATTG[-/C]CAACCTCTGCTTCCT | 54629 |
rs55983371 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856099 | ATATATAGTTTGGAA[A/G]ACTATCCTTAATAGT | 54629 |
rs55985652 | snp | C/G | 0.039522 | 0.134904 | intron-variant | FAM63B | GRCh38.p7 | 15:58786863 | AGATGGAGTTTCACT[C/G]TTGTCACCCAGGCTG | 54629 |
rs56031317 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAM63B | GRCh38.p7 | 15:58845731 | AAATCAGTATATCAA[A/G]GAGATATCTGCACTC | 54629 |
rs56197260 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58785007 | TGTTAATTCTGTATT[C/T]TTAGCCAACTATCTC | 54629 |
rs56286216 | in-del | -/AA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852971 | TTTTTTTTTTTTTTT[-/AA]GACAGAGTCTCACTC | 54629 |
rs56935479 | in-del | -/GTTTT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58835928 | GTTTTGTTTTGTTTT[-/GTTTT]TGAGATGGGGTCTTG | 54629 |
rs57065807 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58806645 | AGCATGAGCCCAGAG[C/G]CATTAGAAATCATAT | 54629 |
rs57170334 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58818669 | TTTTTTTTTTTTTTT[-/T]GAGACAGTGTTTTTG | 54629 |
rs57285066 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | FAM63B | GRCh38.p7 | 15:58833895 | TGGGTGTCGGGCTGC[C/G]GGACGGTCAGGTCTT | 54629 |
rs57308436 | snp | A/G/T | 0.0490924 | 0.148973 | intron-variant | FAM63B | GRCh38.p7 | 15:58826956 | CCTTCCTTTTTTGTC[A/G/T]TTTATGACATTGACT | 54629 |
rs57361212 | in-del | -/TCTAT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58844009 | TGCATTAAAACCTAT[-/TCTAT]ATTATTATTTATGAA | 54629 |
rs57410072 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | FAM63B | GRCh38.p7 | 15:58825886 | GCTGGGATTACAGGC[A/G]TGAGATGCCATACCC | 54629 |
rs57434621 | in-del | -/TTTTTTGTA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58818816 | GGCTAATTTTTTGTA[-/TTTTTTGTA]GAGATGGGGTTTCCT | 54629 |
rs57658375 | in-del | -/AAAT | 0.416708 | 0.186302 | intron-variant | FAM63B | GRCh38.p7 | 15:58795178 | AATAAATAAATAAAT[-/AAAT]CTGTGGAAGTTGATA | 54629 |
rs57743704 | in-del | -/AAAA | | | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769452 | AAAAAAAAAAAAAAA[-/AAAA]GGGGCACAGTCTTCT | 54629 |
rs57744714 | in-del | -/A | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855931 | TCTCAAAAAAAAAAA[-/A]GTCTGAGAGTAGCTA | 54629 |
rs57783587 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58834003 | GTCCCTGCAGCCTTC[C/T]GCAGTGTTTTGTGTC | 54629 |
rs57824507 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58806375 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 54629 |
rs57832322 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861229 | GCAAGGAAGAGAAAC[A/G]AGTTTTCTTTCTCCA | 54629 |
rs57863736 | in-del | -/G/TTTGTTTG/TTTGTTTGTTTG | 0.469544 | 0.119585 | intron-variant | FAM63B | GRCh38.p7 | 15:58839322 | AAGTTAGACTGTTTT[-/G/TTTGTTTG/TTTGTTTGTTTG]TTTGTTTGTTTGTTT | 54629 |
rs57998049 | in-del | -/ATATATATATATATATAT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58791239 | TATATATATATATAT[-/ATATATATATATATATAT]CTTGAGTTCAGAGGA | 54629 |
rs58210669 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | FAM63B | GRCh38.p7 | 15:58815802 | TTCCTGCCTCAGTCT[C/G]CTGAGCAGCTGGGAC | 54629 |
rs58374538 | in-del | -/TT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58787164 | TTTTTTTTTTTTTTT[-/TT]ACTCTGTTGCCCAGG | 54629 |
rs58469477 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | FAM63B | GRCh38.p7 | 15:58844539 | TACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 54629 |
rs58734999 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771154 | AGGGCTGGGCCACGT[G/T]GGCGGCTGCTGAGTG | 54629 |
rs58768604 | in-del | -/TT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58807373 | TTTTTTTTTTTTTTT[-/TT]GAGACCGAGTCTTGC | 54629 |
rs58937576 | snp | A/G | 0.130008 | 0.219321 | intron-variant | FAM63B | GRCh38.p7 | 15:58776375 | AACAGAGGAATAAAG[A/G]TTACACTGGGGAAGG | 54629 |
rs59075081 | in-del | -/AA | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58800852 | AAAAAAAAAAAAAAA[-/AA]GTCTTCTAAAATGTG | 54629 |
rs59102287 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58838352 | GTAGTGAGCCAAGAT[C/T]ATGCCACTGCACTCC | 54629 |
rs59148227 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58812451 | CAAAAAAAAAAAAAA[A/C]GAAATAATAAAGAAT | 54629 |
rs59306702 | in-del | -/GTGTGT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58794391 | TGTGTGTGTGTGTGT[-/GTGTGT]TTTAAGAATAAAATA | 54629 |
rs59471550 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58837540 | AAAAAAAAAAAAAAA[-/A]GGAAACCTTTTTTAA | 54629 |
rs59518143 | in-del | -/G/GTT/GTTT/GTTTGTT/GTTTGTTT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58839321 | TAAGTTAGACTGTTT[-/G/GTT/GTTT/GTTTGTT/GTTTGTTT]TTTTGTTTGTTTGTT | 54629 |
rs59525226 | in-del | -/AA | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58846107 | AAAAAAAAAAAAAAA[-/AA]GAAAAAACAGAATGA | 54629 |
rs59576117 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | FAM63B | GRCh38.p7 | 15:58827526 | TGGAGTGTAGTGGCG[C/T]GATCTCGGCTCACTG | 54629 |
rs59599149 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAM63B | GRCh38.p7 | 15:58812211 | GGGAGGCCGAGGCGG[A/G]TGGATCATGAAGTCA | 54629 |
rs59631822 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | FAM63B | GRCh38.p7 | 15:58848943 | GGCCAGGCAAGGTGG[C/G]TCACACCTATAATCC | 54629 |
rs59647780 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58834738 | GGCTTATTAAAGTCG[A/T]GAATTACATCTTCAT | 54629 |
rs59728603 | in-del | -/C | 0.467337 | 0.123551 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770030 | ACAAAAACAAAAAAA[-/C]ATATAAGTATGTATT | 54629 |
rs59851506 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAM63B | GRCh38.p7 | 15:58835484 | ATGGTGAAACCCCGT[C/T]TTTACTAAAAATACA | 54629 |
rs60120240 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58846615 | AAAAAAAAAAAAAAA[-/A]TCTCATGTAACCCAC | 54629 |
rs60131191 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58813950 | TTTTTTTTTTTTTTT[-/T]AATTTGAGATGGAGT | 54629 |
rs60162496 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58788613 | GCAAGCAGTTGTACA[C/T]CACATTGTGGCCTTT | 54629 |
rs60365490 | in-del | -/AAAAAAAAAAA/AAAAAAAAAAAAAAAAA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852305 | AAAAAAAAAAAAAAA[lengthTooLong]GATGATCACTTTAGC | 54629 |
rs60618257 | in-del | -/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58795766 | CTAAGTTTTTTTTTT[-/T]CTTTTTTTTGGCCAC | 54629 |
rs60627319 | snp | G/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58794360 | AAGTTTTTTTTGGGG[G/T]GTGTGTGTGTGTGTG | 54629 |
rs60825497 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | FAM63B | GRCh38.p7 | 15:58789977 | AGAGATTGGGTTTCA[C/T]TGTGTTTCCCAGGCT | 54629 |
rs61055606 | in-del | -/ATATATATATATAT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58791256 | TATATATATATATAT[-/ATATATATATATAT]CTTGAGTTCAGAGGA | 54629 |
rs61211927 | in-del | -/ATATAT/ATATATATATATAT | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58831060 | TATATATATATATAT[-/ATATAT/ATATATATATATAT]GTTTTAAATTATACC | 54629 |
rs61729219 | snp | A/G | 0.00353536 | 0.0418949 | missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771460 | CCGGGCCAGCGTCAG[A/G]GACAGGTTCTTCGCA | 54629 |
rs62002433 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | FAM63B | GRCh38.p7 | 15:58810710 | TCACCAGAGTGACTA[A/G]CAGGACTCCCTGAAA | 54629 |
rs62002434 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58813929 | AGTTTTAACTTGCAT[C/T]TCTTTTTTTTTTTTT | 54629 |
rs62002454 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58823050 | ACATTACTTAATTAT[C/T]CAGAAGTTTAACACA | 54629 |
rs62002455 | snp | C/T | 0.309894 | 0.242719 | intron-variant | FAM63B | GRCh38.p7 | 15:58835366 | ACATTTAAAATGATA[C/T]CTGAGGCTGGGTGCG | 54629 |
rs62002456 | snp | C/G | 0.31014 | 0.242659 | intron-variant | FAM63B | GRCh38.p7 | 15:58835645 | GCGACAAGAGCGAAA[C/G]TCTGTCTCAGTAATT | 54629 |
rs62002457 | snp | G/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58841591 | TGTACTTTTAGTAGA[G/T]ACACAGTTTCACCAT | 54629 |
rs62002458 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58846346 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCTGA | 54629 |
rs62002459 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58846355 | TCCCAGCACTTTGGG[A/G]GGCTGAGGCGGGTGG | 54629 |
rs62004762 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | FAM63B | GRCh38.p7 | 15:58854183 | CAGGAAGTGGAGGTT[A/G]CAGTGAGACAAGATT | 54629 |
rs62004763 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857242 | GATACTGGTTTCCTG[A/C]CCTTGAAGGGTATAA | 54629 |
rs62004764 | snp | A/T | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857558 | AAAAAAAAAAAAATT[A/T]GAGCTATTGTGTCTT | 54629 |
rs66488066 | in-del | -/CTATT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58844005 | TTAATGCATTAAAAC[-/CTATT]CTATATTATTATTTA | 54629 |
rs66919821 | in-del | -/ATATATATATATATATATACAC | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58831042 | TATATATATATATAT[-/ATATATATATATATATATACAC]ACACACACACACACA | 54629 |
rs67438612 | in-del | -/C | 0.0588605 | 0.161139 | intron-variant | FAM63B | GRCh38.p7 | 15:58848594 | TAAAAATATAAAAAT[-/C]AATTATCCGGGCATG | 54629 |
rs67476667 | in-del | -/A | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58807373 | GCAAGACTCGGTCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs67582319 | in-del | -/TAGA | 0.375 | 0.216506 | intron-variant | FAM63B | GRCh38.p7 | 15:58774561 | TGTCTGTCATCCCAC[-/TAGA]TAGTCAGCTACACGA | 54629 |
rs67590689 | in-del | -/CT | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58840382 | ATTCTGGAAAAATAC[-/CT]CTGTGTTTCTTTCAT | 54629 |
rs67601600 | in-del | -/A/AA | 0.625 | 0.125 | intron-variant | FAM63B | GRCh38.p7 | 15:58798472 | GTGAAACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAT | 54629 |
rs67908953 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58803311 | AAAATACAAAAAAAA[-/A]TTAGCTGGGCATGGT | 54629 |
rs71116602 | in-del | -/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58789691 | CATTGCACTCCAGCC[-/T]TGAGAAACAAGAGTG | 54629 |
rs71119403 | in-del | -/ACACACAC | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58791661 | TACACACACACACAT[-/ACACACAC]ACACACACACACACA | 54629 |
rs71119407 | in-del | -/AAAAAC/AAACAAAC/CAACAAAC/TAAC | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58839345 | GACTTCATCTCAAAA[lengthTooLong]AAACAAACAAACAAA | 54629 |
rs71119408 | in-del | -/AAT | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58840672 | AAGACTCCATCTCAA[-/AAT]AATAATAATAATAAT | 54629 |
rs71297612 | in-del | -/AGGATCA | 0.479904 | 0.0982045 | intron-variant | FAM63B | GRCh38.p7 | 15:58814615 | GGAGGCTGAGGAGGG[-/AGGATCA]TTTGAGCCCAGGAGT | 54629 |
rs71478691 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58784922 | CTGTAGACGTGAGCC[A/C]CCGTACCCAGCCTGT | 54629 |
rs71478692 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAM63B | GRCh38.p7 | 15:58811261 | ATTTATTTTAAAAAG[G/T]CACCCCCATATATCC | 54629 |
rs71478693 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAM63B | GRCh38.p7 | 15:58829264 | ATGACAGGAGAATTA[C/T]GAAACATTGTTTTTT | 54629 |
rs72001552 | in-del | -/AA | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857554 | AAAAAAAAAAAAAAA[-/AA]ATTAGAGCTATTGTG | 54629 |
rs72332455 | in-del | -/A | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58801441 | GTAGAAAATTCAAAG[-/A]AAAAAGTATGTACAT | 54629 |
rs72518541 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58807354 | CATTTTAAAATAGTC[-/T]TTTTTTTTTTTTTTT | 54629 |
rs72745027 | snp | A/G | 0.391954 | 0.205789 | intron-variant | FAM63B | GRCh38.p7 | 15:58802130 | TAGTATATACATTGA[A/G]AAAATATTTGACGTG | 54629 |
rs72745037 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | FAM63B | GRCh38.p7 | 15:58816359 | TGTGAAGAATGACAG[A/T]CTGAGGAATGTAAGC | 54629 |
rs72745038 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58822564 | TATATTTCAGTATAA[A/T]ACAATATTAAAGCCC | 54629 |
rs72745042 | snp | G/T | 0.411242 | 0.191052 | intron-variant | FAM63B | GRCh38.p7 | 15:58839346 | TTTGTTTGTTTGTTT[G/T]TTTGAGATGAAGTCT | 54629 |
rs72745044 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FAM63B | GRCh38.p7 | 15:58849971 | CGAACTCCTGGGCTC[A/G]AGTGATGTGCCCGCC | 54629 |
rs73426583 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58785236 | TCCACAGTATTAGTG[A/T]GAAGTAGGCACTTTT | 54629 |
rs73426593 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58792334 | ATGTTCAGGCCACAC[A/G]CGGTGGCTTACGCCT | 54629 |
rs73426598 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58800761 | ATCACCTGAGTCTAG[A/G]GAGGTTGAGGTTGCA | 54629 |
rs73426599 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58801297 | CTTTTACAGTTCAAT[A/C]AGAAAAGATAGGCCA | 54629 |
rs73428510 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58809743 | TGTTTATCTCTCCCA[A/G]TAGAATGTTAGTTGC | 54629 |
rs73428513 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58810544 | CAGAGTCCTCCAGAC[C/T]ACTAAGTCTGCCCAA | 54629 |
rs73428515 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58810569 | GCCCAAGGCTTCTGA[C/T]CCCAACTCTAAGGAG | 54629 |
rs73428524 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58815649 | CACTGTGCTTGGCTC[A/G]AGAAGAAAGGATATT | 54629 |
rs73428529 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58819880 | GTACATAGAATCTTA[A/T]CCCAAGGATCCTCTC | 54629 |
rs73428533 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58821198 | CAGGAAAATAACATT[A/G]GTTATCTCTACTCAT | 54629 |
rs73428535 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58821323 | GTGCAACATTTGTTT[C/T]TTAGTTAAAAAAAAA | 54629 |
rs73428543 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAM63B | GRCh38.p7 | 15:58824173 | GTAGGACTTAGTACT[A/G]TAATAATTAACAAAA | 54629 |
rs73428554 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58836220 | CGGCCTATTGCATCT[C/G]AAAATTAACTATAAT | 54629 |
rs73428557 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58837730 | CAGTACTTTGAGAGG[C/T]AGAGGTGGGAAGATC | 54629 |
rs73428561 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58840239 | TATCTACCACACTTC[C/T]GAACGAATATAGTAC | 54629 |
rs73428564 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | FAM63B | GRCh38.p7 | 15:58842066 | CCCCTGTCTAGATCA[C/T]ATAGCTTCTAGATCT | 54629 |
rs74021005 | snp | C/T | 0.0627361 | 0.166206 | intron-variant | FAM63B | GRCh38.p7 | 15:58786166 | TAAAAACTTATTTTA[C/T]TTGTTGATTAAAACA | 54629 |
rs74021006 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | FAM63B | GRCh38.p7 | 15:58798849 | AGTATACTCTAACCA[C/T]GAAAATGTCAGCATG | 54629 |
rs74021007 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | FAM63B | GRCh38.p7 | 15:58800394 | TTCACTCCTCTACTT[A/G]AAAGTATAAAGATCC | 54629 |
rs74021008 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAM63B | GRCh38.p7 | 15:58818050 | TTCTATGGAATACTG[C/T]ACTACAGTGAAAACA | 54629 |
rs74021010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58822788 | CACTCTTTCAAAAAT[A/G]TACATAAATACTGAG | 54629 |
rs74021012 | snp | A/C/T | 0.0174175 | 0.0916809 | intron-variant | FAM63B | GRCh38.p7 | 15:58825375 | ACTGCTTTCGGGTGT[A/C/T]GATACCTTTTTTATT | 54629 |
rs74021013 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | FAM63B | GRCh38.p7 | 15:58827382 | TTTATTAGTTGTTAT[G/T]CTTCTGTAACAGAAC | 54629 |
rs74334714 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | FAM63B | GRCh38.p7 | 15:58775188 | GTCAGTTAATGCAAT[A/G]TGTGCCTCTGTACTT | 54629 |
rs74384075 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769595 | GGGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG | 54629 |
rs74433086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAM63B | GRCh38.p7 | 15:58800325 | CTGTATCATTCTTTG[C/T]CCCTAAATTAGCCTA | 54629 |
rs74434997 | snp | A/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58827441 | TCCCCATTAAAAAAA[A/T]TTGTATCCATATAAA | 54629 |
rs74438033 | snp | A/C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769615 | ACGAGGTCAGGAGAT[A/C/T]AAGACCATCCTGGCT | 54629 |
rs74570429 | snp | A/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58827629 | CCACCACGGCCGGCT[A/T]ATTTTTTTGTACTTT | 54629 |
rs74601258 | snp | A/G | 0.0163317 | 0.088877 | intron-variant | FAM63B | GRCh38.p7 | 15:58802429 | AGTTTAAATATATAC[A/G]TTGGTTTCTATTAGT | 54629 |
rs74641422 | in-del | -/T | 0.0479149 | 0.147179 | intron-variant | FAM63B | GRCh38.p7 | 15:58823140 | AATCTTTTTTTTTTC[-/T]TTTTTTTTTTTTTTG | 54629 |
rs74666311 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FAM63B | GRCh38.p7 | 15:58819028 | GCATTGCCCAGGCTG[A/G]TGTGTAGTAGCATGA | 54629 |
rs74722595 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAM63B | GRCh38.p7 | 15:58777804 | TTTTGTTGTTTTTTT[A/G]TGGAGACGGGGTCTC | 54629 |
rs74747971 | snp | G/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58826245 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTTTTG | 54629 |
rs74926492 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58859304 | TTCTCCATGGAATAC[A/G]GTGGTATCAAATTAC | 54629 |
rs74927354 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58833845 | AGGATTAGTATAAGA[A/G]GAAGGCATGCCTCTT | 54629 |
rs74929056 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58846106 | TTAAAAAAAAAAAAA[A/G]AGAAAAAACAGAATG | 54629 |
rs74930022 | snp | A/C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769616 | CGAGGTCAGGAGATC[A/C/G]AGACCATCCTGGCTA | 54629 |
rs74938175 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58843555 | AATGAAAACCTATTC[C/T]GTCCAGAAATACCCT | 54629 |
rs74988264 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852308 | AAAAAAAAAAAAAGA[A/T]GATCACTTTAGCAGT | 54629 |
rs75155934 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769675 | ATACAAAAAGTTAGC[C/T]GGGCGTGGTGGCGGG | 54629 |
rs75167644 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58787739 | GAGAGTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA | 54629 |
rs75174016 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | FAM63B | GRCh38.p7 | 15:58825924 | GAATGTTTCTTTAAC[A/G]GTTGTTCCTAGGACA | 54629 |
rs75245806 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | FAM63B | GRCh38.p7 | 15:58780009 | TATTTTTGTGTCCAG[A/T]TACTGTGCATTATTT | 54629 |
rs75269616 | snp | A/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58827631 | ACCACGGCCGGCTAA[A/T]TTTTTTGTACTTTTA | 54629 |
rs75288886 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAM63B | GRCh38.p7 | 15:58777340 | AAATCAATAGACTGA[A/G]CAAACCGGGAGGATT | 54629 |
rs75290054 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58854243 | TGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAGG | 54629 |
rs75301953 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58779763 | ACTCTGGATTTGTAA[G/T]ATAAGGTAGACAAGG | 54629 |
rs75343291 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769669 | CTAAAAATACAAAAA[A/G]TTAGCTGGGCGTGGT | 54629 |
rs75388688 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769610 | AGATCACGAGGTCAG[A/G]AGATCAAGACCATCC | 54629 |
rs75400379 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58785392 | AATGCAGAGATCAGC[A/G]AACTTTTTCTGTAAA | 54629 |
rs75610789 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | FAM63B | GRCh38.p7 | 15:58825605 | TGTGGTGTTTGTTTG[A/T]TTGTTTGTTTTGAGA | 54629 |
rs75618038 | snp | C/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58800664 | TGCATCCAGTTTAGC[C/T]TTTTTTTTTTTTTGA | 54629 |
rs75735558 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803484 | AAAAAAAAAAAAAAA[A/G]AAGAAGAATCAACAA | 54629 |
rs75870720 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58814910 | AGCCTCTCAGAGTGC[C/T]GAGGTTACAAATGTG | 54629 |
rs75888243 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | FAM63B | GRCh38.p7 | 15:58788191 | TAAGGAATCTAGGTA[A/C]CGTCTAGAAAACAAG | 54629 |
rs75994534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58847814 | AAGAAGGAAACAGGT[C/G]TAAGCAGAGACAAAT | 54629 |
rs75998310 | snp | G/T | 0.0123036 | 0.0774623 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861105 | CCTAAAGCTAGTGCG[G/T]GTGAATCTTTTCCTT | 54629 |
rs76035762 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58828455 | TTTCTATTCCTTTTT[C/G]ACTAATTATAGTACC | 54629 |
rs76096523 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58799580 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAAG | 54629 |
rs76143135 | snp | G/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58784638 | TTTTTTTTTTTTTTT[G/T]AGATCGGATCTCTCT | 54629 |
rs76193371 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58786116 | ATATATGCTTACAGA[A/T]GGCTTCAAACCATTC | 54629 |
rs76250279 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770032 | AAAAACAAAAAAACA[A/T]ATAAGTATGTATTAA | 54629 |
rs76344785 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769548 | ATGTGTGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 54629 |
rs76407709 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58825756 | GACTACAGGCTCACG[C/G]CACCACGCTGGCTAA | 54629 |
rs76450037 | snp | A/C | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58854245 | CAAGACTCTGTCTCA[A/C]AAAAAAAAAAAGGAA | 54629 |
rs76476189 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | FAM63B | GRCh38.p7 | 15:58812617 | GTAATCCTAGAACTT[C/T]GGGAGGCCAAGGCAA | 54629 |
rs76514889 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAM63B | GRCh38.p7 | 15:58848259 | ATTTAAGTGCACAAA[A/G]ACTGTTCAGTTAGCC | 54629 |
rs76631723 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | FAM63B | GRCh38.p7 | 15:58839818 | TTTATTTTTACCACA[C/G]CTGATTTTATCTTTT | 54629 |
rs76632872 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58838889 | CCCGGCCTAATTTTT[A/T]TTACGACTTTTCAGA | 54629 |
rs76655921 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769680 | AAAAGTTAGCTGGGC[A/G]TGGTGGCGGGCGCCT | 54629 |
rs76658691 | snp | C/G | 0.334182 | 0.235401 | intron-variant | FAM63B | GRCh38.p7 | 15:58802664 | GAGAGATCAAACCTA[C/G]TGTTTTTCTTGAAAA | 54629 |
rs76751232 | snp | A/G/T | 0.18325 | 0.240924 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857557 | AAAAAAAAAAAAAAT[A/G/T]AGAGCTATTGTGTCT | 54629 |
rs76846614 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58803482 | ATAAAAAAAAAAAAA[A/G]AGAAGAAGAATCAAC | 54629 |
rs76901380 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770805 | CTTAATTTTCCATAT[C/T]AGGAGCTGAGAAACC | 54629 |
rs76924300 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | FAM63B | GRCh38.p7 | 15:58826530 | CACTGCACCTGGCCC[C/G]ACACACTCTTTTTCC | 54629 |
rs76961741 | snp | A/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58846680 | AAAAATTAAAAAAAA[A/T]TTTGTATGCACGTAC | 54629 |
rs76971771 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58778539 | AAACAGACACACACC[A/C]AAAAAAAAAACCTCA | 54629 |
rs76986256 | snp | A/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58785157 | AAAAAAAAAAAAAAA[A/G]AGAAAAGCAAGCTTT | 54629 |
rs77064120 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | FAM63B | GRCh38.p7 | 15:58782742 | GGTGTCTGATCTCAC[G/T]TCTCATCACAGTACT | 54629 |
rs77082298 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855920 | GGGAGACTCCGTCTC[A/C]AAAAAAAAAAAGTCT | 54629 |
rs77144915 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58854244 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAGGA | 54629 |
rs77386417 | snp | A/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58779063 | CACTGTGCCCAACCA[A/T]TTTTTTTTTTTTCTC | 54629 |
rs77391075 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAM63B | GRCh38.p7 | 15:58796318 | GAGGTGGAAATATGT[A/G]AGGCATATTGAAGGA | 54629 |
rs77521060 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | FAM63B | GRCh38.p7 | 15:58811386 | TGGCAGGAAGTAGAC[G/T]ACACACTGAAGGATA | 54629 |
rs77637863 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | FAM63B | GRCh38.p7 | 15:58776758 | CGTGTGTGGTGGCTC[A/G]TGCCTGTCGTCCCAG | 54629 |
rs77656700 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58837081 | TGCTAAATAAAATTT[A/G]GGGAAGGGGTTCTTC | 54629 |
rs77713295 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FAM63B | GRCh38.p7 | 15:58815214 | GTTATTCTTACCCTG[A/T]TGAATTGTCTTGAAC | 54629 |
rs77748075 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | FAM63B | GRCh38.p7 | 15:58794452 | ACAGACAGGCAGGGT[A/G]TTGGAAGAGACATCT | 54629 |
rs77779287 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769664 | CTCTACTAAAAATAC[A/C]AAAAGTTAGCTGGGC | 54629 |
rs77894675 | snp | C/T | 0.14665 | 0.227637 | intron-variant | FAM63B | GRCh38.p7 | 15:58844610 | ACAGTGAACCAGTTA[C/T]AGTTTTTTTAAAAAA | 54629 |
rs77904473 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58831515 | AAATCCTTTGTAATA[C/G]TAGGTGAAGTATAAG | 54629 |
rs77976434 | snp | C/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58847524 | TGATTTTTTTCAAAT[C/G]TGAATTCATGTATCC | 54629 |
rs78122215 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58821143 | AAATAAGAATCATGG[C/T]GCATATCCCATCCCC | 54629 |
rs78172344 | snp | A/G | 0.125182 | 0.216612 | intron-variant | FAM63B | GRCh38.p7 | 15:58784275 | AGGCTGCAGTGTGCC[A/G]TGATCCTGCCACTGC | 54629 |
rs78268932 | snp | A/C | 0.335559 | 0.234904 | intron-variant | FAM63B | GRCh38.p7 | 15:58795402 | TATATAGTATGTGTT[A/C]TTTTGTTTTGTTTTG | 54629 |
rs78275471 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58818319 | GCTAGAGTGCAGTGG[C/T]GTGATCATAGCTCAC | 54629 |
rs78322328 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769647 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 54629 |
rs78326613 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58798473 | ATTTTTTTTTTTTTT[G/T]AGACAGAGTTTCACT | 54629 |
rs78379983 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769570 | TCACGCCTGTAATCC[C/T]AGCACTTTGGGGGCC | 54629 |
rs78462800 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769987 | GAGAGAGACTCCGTT[A/T]CAAAAAAAAAAAAAA | 54629 |
rs78586819 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852306 | AAAAAAAAAAAAAAA[A/G]ATGATCACTTTAGCA | 54629 |
rs78589757 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | FAM63B | GRCh38.p7 | 15:58819538 | TATTTTTAGAGACAG[A/G]AGTTTTGCTGTGTTA | 54629 |
rs78778748 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | FAM63B | GRCh38.p7 | 15:58784917 | TGGGACTGTAGACGT[A/G]AGCCACCGTACCCAG | 54629 |
rs78780638 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | FAM63B | GRCh38.p7 | 15:58830393 | CTAATCTGAAAATCC[A/G]AAATCCAAAATGCTC | 54629 |
rs78782067 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852309 | AAAAAAAAAAAAGAT[A/G]ATCACTTTAGCAGTA | 54629 |
rs78823058 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769543 | ATATTATGTGTGGCC[A/G]GGCATGGTGGCTCAC | 54629 |
rs78846635 | snp | C/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58802310 | CTTTTTTTTTTTTTA[C/T]AGGAGATTACATGCT | 54629 |
rs78851944 | snp | G/T | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58852946 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 54629 |
rs78856239 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | FAM63B | GRCh38.p7 | 15:58776832 | TTTGAGACCAGCTGG[A/G]GCAATATAGTGAGAC | 54629 |
rs78871054 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | FAM63B | GRCh38.p7 | 15:58824487 | TTATATGTGTCATTT[A/T]GCATAATTAAAAAGC | 54629 |
rs79046137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58847665 | AGAAGGCCAGATCAT[A/G]TTGAACTGTGAAGGT | 54629 |
rs79198733 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58859685 | GGCCAGATGCAGGAC[C/T]CTGGTAAATTTAACT | 54629 |
rs79331191 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58806885 | TGAGAAAATATGTTG[A/T]TTGGGGGGAACAGTA | 54629 |
rs79378213 | snp | C/T | 3.35278e-05 | 0.00409424 | missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772093 | AGGTGCTGGCGGCCT[C/T]CAAGGAACGCTTCCC | 54629 |
rs79391556 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | FAM63B | GRCh38.p7 | 15:58818548 | GACATGAGCCACTAC[A/G]CCTGGCCTTGAGTGA | 54629 |
rs79402553 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | FAM63B | GRCh38.p7 | 15:58822983 | GGAGCATATGAGCAT[A/G]TAAAAGATATGTACA | 54629 |
rs79491470 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAM63B | GRCh38.p7 | 15:58816666 | GATAGAACTAGGGCA[C/T]TCTAGAGCAATGGGG | 54629 |
rs79510174 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FAM63B | GRCh38.p7 | 15:58778061 | GAAGGTATATAACAT[A/G]TATATTTTAGTGCTT | 54629 |
rs79512009 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | FAM63B | GRCh38.p7 | 15:58795845 | AGTGCAACATTACCT[C/G]TGCTAAAATGCATGA | 54629 |
rs79513234 | snp | A/C | 0.00101659 | 0.0225225 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | FAM63B | GRCh38.p7 | 15:58831803 | CAGTTTCTAAATAAC[A/C]CAGCCACTCAACTGA | 54629 |
rs79523831 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769590 | CTTTGGGGGCCGAGG[C/T]GGGCAGATCACGAGG | 54629 |
rs79553102 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FAM63B | GRCh38.p7 | 15:58796934 | TACTTTCCTTGTTCT[C/T]AGATGGAATTGTGTA | 54629 |
rs79714616 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58802309 | TCTTTTTTTTTTTTT[A/C]CAGGAGATTACATGC | 54629 |
rs79878883 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58808504 | TTCTTTACTACTACG[C/T]ATTTAAGTTTCCTCT | 54629 |
rs79896529 | in-del | -/AA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852307 | AAAAAAAAAAAAAGA[-/AA]TGATCACTTTAGCAG | 54629 |
rs79904206 | snp | A/C/T | 1.84504e-05 | 0.00303724 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771590 | GAGGAGCCTCCCGGA[A/C/T]TCGGCTTCTCCCGCG | 54629 |
rs80000489 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855919 | AGGGAGACTCCGTCT[A/C]AAAAAAAAAAAAGTC | 54629 |
rs80076887 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAM63B | GRCh38.p7 | 15:58809218 | CCCTATATTCATCAA[A/G]CAACCCCCCTTTTCC | 54629 |
rs80113584 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769547 | TATGTGTGGCCGGGC[A/G/T]TGGTGGCTCACGCCT | 54629 |
rs80211319 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | FAM63B | GRCh38.p7 | 15:58822961 | AGAATTAAAACTAAC[A/G]ACTACAGGAGCATAT | 54629 |
rs80294760 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58769585 | TAGCACTTTGGGGGC[C/T]GAGGTGGGCAGATCA | 54629 |
rs111263608 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58823689 | CAAAACAAAACAAAA[A/C]AAAAAACAGTATAGA | 54629 |
rs111332586 | in-del | -/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58790255 | TATTATTATTTTAAG[-/T]TTTTTTTTTCCCCAT | 54629 |
rs111380414 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAM63B | GRCh38.p7 | 15:58805868 | ATCACAAGGTCTGGA[A/G]ATCGAGACCATGCTG | 54629 |
rs111458504 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58782284 | ATATATACACACATG[A/T]GTATATACACTGCAT | 54629 |
rs111515685 | snp | C/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58813553 | TCTGGGTTAAATGCC[C/T]AGGAGTGCAGTTGGT | 54629 |
rs111525768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58807499 | TAGCTGAGAGAGACT[A/G]CAGGCGCCCGCCATC | 54629 |
rs111563124 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58780410 | TCCATCTCAAAAAAA[A/C]AAAAGAAAGAAAATT | 54629 |
rs111579799 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | FAM63B | GRCh38.p7 | 15:58838691 | TCTCAGGTTCAAGCG[A/T]TTGTCCTGCCTCAGC | 54629 |
rs111648865 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | FAM63B | GRCh38.p7 | 15:58817245 | TATTCAGAAAGTAGG[A/G]GCTCCTACAGATAAT | 54629 |
rs111689296 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | FAM63B | GRCh38.p7 | 15:58781394 | TCACTGCAACAACAT[G/T]CTTTATTGCTCTAAA | 54629 |
rs111724931 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58824833 | TGCCACCATGCCCGA[C/T]TAATTTTTGTATTTT | 54629 |
rs111781637 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58816469 | AGACTAGAGTGCAGT[A/G]GTGTGATCATAGCTC | 54629 |
rs111782147 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FAM63B | GRCh38.p7 | 15:58780301 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 54629 |
rs111795343 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58798386 | CACCTTACACTCTCA[A/G]AGTGCTGGGACTACA | 54629 |
rs111836391 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | FAM63B | GRCh38.p7 | 15:58805794 | TTAAGACAGAGTCTC[A/G]GCTGGGCACAGTGGC | 54629 |
rs111967960 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58837209 | CCTACTAATTCCTGA[A/G]TTGTTTGTAGCACTT | 54629 |
rs112011499 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58819063 | AGCTCATTGCAGCCT[C/T]GAACTCCTGGACTCA | 54629 |
rs112037045 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58776991 | ATTAAGATTGTAAAG[C/T]ATTTGACCCGGTGAA | 54629 |
rs112068235 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58848825 | ACAGTTCTGAAAGTC[A/G]TGCTCATTTTCCTTC | 54629 |
rs112108726 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | FAM63B | GRCh38.p7 | 15:58845109 | GACATTTCTCCAAAG[A/C]AGTCATGCAAATGAG | 54629 |
rs112165316 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | FAM63B | GRCh38.p7 | 15:58850693 | GCCTCAAGTGATCCT[C/T]CCACCTCAGCCTCCC | 54629 |
rs112242365 | snp | G/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58794397 | TGTGTGTGTGTGTGT[G/T]TTAAGAATAAAATAT | 54629 |
rs112256219 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855808 | GTGCCTGTAGTCCCA[G/T]CTACTCAGGGCTGAG | 54629 |
rs112257595 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58823929 | ATAATTACTAAAAAG[A/G]AGCTCCTATTTTAAA | 54629 |
rs112297028 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58795974 | GAAGAAAGGAGAAAG[C/G/T]GTATTGAATACTGGA | 54629 |
rs112299611 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | FAM63B | GRCh38.p7 | 15:58843214 | GAGTACAGTGGCACA[A/G]TCTTGGCTCACTGGA | 54629 |
rs112301856 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58777587 | GAGACCAGCCTGGTC[A/C]ACATAATGAGACCCC | 54629 |
rs112303345 | in-del | -/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58847202 | GGAATGTTTAATATA[-/T]TCTGAAGATACAGAT | 54629 |
rs112322674 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58792294 | AAGAGAAGTGAAAAC[A/G]TATGTCCATACAGCT | 54629 |
rs112337987 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58823784 | TTAGGAGAGAAAGAA[A/G]CAATAAAAACTATTA | 54629 |
rs112355711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58814183 | GACTTCAGGTGATCC[A/G]CCCGCTTCGGCCTCC | 54629 |
rs112399136 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58789082 | GTGGCTCACGCCTGT[A/T]ATCCCAGCACTTTGG | 54629 |
rs112417080 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | FAM63B | GRCh38.p7 | 15:58817531 | AGGAGTTTGAGACGC[C/T]TGGCCAACATGGTGA | 54629 |
rs112451048 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | FAM63B | GRCh38.p7 | 15:58838658 | GTGGCACAATCTCAG[C/T]TCACCACAACCTCCA | 54629 |
rs112518361 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58837354 | AAGGCTGGACAGTCG[C/T]TTGAGGCCCAGAGTT | 54629 |
rs112521870 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58818856 | GTGTTGGCCAGGCTG[C/G]TCTGGAACTGCTGAC | 54629 |
rs112537713 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | FAM63B | GRCh38.p7 | 15:58805939 | AATTAGCTGGGCGTG[G/T]TGGCACGTACTGTGG | 54629 |
rs112685813 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58841390 | TCTATGAAGATAATA[A/C]GCTTTTCCTTTCTTT | 54629 |
rs112713900 | snp | C/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58817827 | GTGGAAATTGGCCAT[C/T]TACTTTTGAAACCAG | 54629 |
rs112724162 | snp | A/T | 0.0456336 | 0.143994 | intron-variant, downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58832265 | GAATTTCGCTCTTGT[A/T]GCCCAGGCTGGAGTG | 54629 |
rs112768809 | snp | A/C | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58847057 | CATACATTAGCTGAA[A/C]ATGCCAAGAGCTCTT | 54629 |
rs112824175 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58789801 | TACAGGCATGCACCA[A/C]CACACGTGGCTAATT | 54629 |
rs112892709 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58788942 | GCTTGAACTCAAGAG[G/T]TGGAGGTTACAGTGA | 54629 |
rs112902442 | snp | C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58782942 | TTTTTTTTTTTGAGA[C/G]AGAGTCTTGCTCTGT | 54629 |
rs112921554 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58789154 | CATCCTGGCTAACAC[A/G]GTGAAACTCCGTCTC | 54629 |
rs112925355 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | FAM63B | GRCh38.p7 | 15:58833789 | ATTCCATTGCTCAGG[A/G]ACAAGCAGGAGACAG | 54629 |
rs112936799 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58785776 | CCGCCTCCCGGGTTC[A/G]AGCAATTCTCCTGCC | 54629 |
rs112970180 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58837813 | TGTACAAAAAACTTT[A/T]AAAAAATTAGCCAGG | 54629 |
rs113082743 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | FAM63B | GRCh38.p7 | 15:58790586 | TTGACAATAGACCTT[-/A]GTGGGGGGTAAGACA | 54629 |
rs113111487 | in-del | -/G | 0 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58807529 | CATGCCTGGCTAAAA[-/G]TTTTTTGTATTTTTT | 54629 |
rs113113774 | snp | A/G | 0 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855816 | AGTCCCAGCTACTCA[A/G]GGCTGAGGCAGGAGA | 54629 |
rs113169830 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58804703 | TCCCAGCTACTTGGG[A/G]GGCTGAGGTCAGAGG | 54629 |
rs113171003 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58774492 | CCCGTCCCAAAAAAA[A/G]AAAAAAAAAAAAAAA | 54629 |
rs113205642 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58774747 | TGGGCAAAGAGAATA[A/G]TGTATTGAAAGATAC | 54629 |
rs113275011 | snp | G/T | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58781514 | TGGTCTTACTCTGAG[G/T]ATAGGGTCTAAATTA | 54629 |
rs113279513 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58803598 | AAGGTGGATGGGTCA[C/T]TTGAGGCCAGGAGTT | 54629 |
rs113288107 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58816430 | TTGTTTGTTTTTTTG[A/G]GACAAGATCTTGCTC | 54629 |
rs113289264 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58798180 | GGAGTATAATGGTGC[A/G]ATCTTGGCTCATTGC | 54629 |
rs113381679 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58817492 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 54629 |
rs113402252 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58805057 | ATACACTCCCATTAC[A/G]CTGATCAGGATTCTT | 54629 |
rs113590674 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855823 | GCTACTCAGGGCTGA[A/G]GCAGGAGAATTGCTT | 54629 |
rs113646452 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | FAM63B | GRCh38.p7 | 15:58801426 | ATGATAATTATATAG[A/G]TAGAAAATTCAAAGA | 54629 |
rs113657074 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAM63B | GRCh38.p7 | 15:58799138 | GGCAAAGAAATTCTG[A/G]AGGCTCTGCCTCACC | 54629 |
rs113710021 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58839900 | TGCAGTGGAGCAATC[G/T]CAGCTCACTGCAACC | 54629 |
rs113714987 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | FAM63B | GRCh38.p7 | 15:58837096 | AGGGAAGGGGTTCTT[C/G]CAGCATGGTGTCCAT | 54629 |
rs113721636 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58808824 | TTAGCCAAGATGGTC[C/T]TGATCTCCTGACCTC | 54629 |
rs113799386 | snp | A/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58826712 | TTTAATATATTGTTC[A/G]TATCAGAATTCTCCC | 54629 |
rs113800059 | snp | C/G | 0.5 | 0 | intron-variant | FAM63B | GRCh38.p7 | 15:58853645 | CCAATATGATGAAAC[C/G]CTGTCACTACTAAAA | 54629 |
rs113831034 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | FAM63B | GRCh38.p7 | 15:58777759 | CTCTCATTTTCAAGA[C/G]ATAGTTTCATCTACC | 54629 |
rs113854050 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58851657 | TATTGCCCAGGCCTG[G/T]TGTATTTTTTAATAG | 54629 |
rs114030759 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | FAM63B | GRCh38.p7 | 15:58828559 | CAGTTTAATGAACTA[A/T]TTTATTATTGAATTT | 54629 |
rs114172573 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FAM63B | GRCh38.p7 | 15:58830429 | TCTAAACACCAACAT[A/G]ACGCTCACAGGAAAT | 54629 |
rs114340524 | snp | C/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58800028 | AAAAAATTATTTTAT[C/G]TTTTGAATATAAATA | 54629 |
rs114351544 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAM63B | GRCh38.p7 | 15:58833753 | GTAGATGGAGTATAC[A/G]ATCGGGCTTTACACC | 54629 |
rs114411510 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAM63B | GRCh38.p7 | 15:58843055 | ACTCTCTTAGAAATG[C/T]ATAAATTTTCAAATT | 54629 |
rs114416931 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58853298 | GAAATTCTGATTTGG[C/G]CATACAAGAAAGCAA | 54629 |
rs114439761 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAM63B | GRCh38.p7 | 15:58789941 | CGTGAGCCACCGTGC[C/T]TGGTTAAGTTTTATT | 54629 |
rs114634572 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58825162 | AACATTTTATTTCCT[A/T]TCAAGGTATGAGGAA | 54629 |
rs114669283 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAM63B | GRCh38.p7 | 15:58817781 | TGGTGAAGATGTGCA[A/G]CATAGAGAATTCTCA | 54629 |
rs114688542 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58785628 | ATGGGAACTCTCTGT[A/G]CTTTCTGCCCAGTTT | 54629 |
rs114788354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58813775 | AGAAAGCGACAAACT[A/G]TTTACTAGATTACCT | 54629 |
rs114867956 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAM63B | GRCh38.p7 | 15:58819895 | TCCCAAGGATCCTCT[C/T]GCAAAGAAAAGGATT | 54629 |
rs114941356 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58807662 | GCCATTGCGCCCGGC[C/T]TAAAATAGTCTTTAT | 54629 |
rs114962095 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771019 | CAACTTCCGGCCACA[C/T]AGTGAGAGGATGTTT | 54629 |
rs115051410 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58792022 | GAGAGATGAGCTGAA[C/T]CAAATGCTGCTAATA | 54629 |
rs115055093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58779888 | TAGTTAAAAACCTTC[C/T]CACTCCCCATTCAAC | 54629 |
rs115081155 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAM63B | GRCh38.p7 | 15:58779372 | CCAGGGCTGAGTTTT[C/T]GCTCTATTTCTCCCT | 54629 |
rs115084721 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58808176 | CACTGTCAACATCCC[A/G]CATCAGAGTGGTTCA | 54629 |
rs115112984 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | FAM63B | GRCh38.p7 | 15:58793560 | TTGTACATTTTAAGT[A/G]AGTAGCTTGTATCGT | 54629 |
rs115139464 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAM63B | GRCh38.p7 | 15:58810818 | GCAGAATCTAGGAGG[A/G]TTCCAACTGTGAAGC | 54629 |
rs115230400 | snp | C/G | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58820855 | AAGAAAACATTGGCC[C/G]TCTTATTTTTATTTA | 54629 |
rs115234258 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAM63B | GRCh38.p7 | 15:58832897 | GAAGAAATAAATTTA[C/T]TTATTTATTTAGATG | 54629 |
rs115371007 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58805271 | GTCTAAGCTAATGTG[C/T]AATGTTCCACAAGTG | 54629 |
rs115466037 | snp | A/C/T | 0.00875189 | 0.0656212 | intron-variant | FAM63B | GRCh38.p7 | 15:58798241 | CCTGCCTCAGCTACC[A/C/T]GAGCAGCTGGGATTA | 54629 |
rs115478219 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | FAM63B | GRCh38.p7 | 15:58825977 | TCTAGGATATGTATT[C/T]GTTAATTCAAATATT | 54629 |
rs115544878 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58782261 | CATGCTGAATATATA[A/G]ATGCTACATATATAC | 54629 |
rs115612944 | snp | A/C | 0.0715223 | 0.175059 | intron-variant | FAM63B | GRCh38.p7 | 15:58809867 | TCACTGCAACCTACA[A/C]CTACTGGGTTCAAGT | 54629 |
rs115620640 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | FAM63B | GRCh38.p7 | 15:58816867 | CTGAGGTAGGAGAAT[C/G]ACTTAAGGCCAGGAG | 54629 |
rs115729496 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | FAM63B | GRCh38.p7 | 15:58791456 | CCCCATCTCCACTTA[A/G]AAATTCAAAAATTAG | 54629 |
rs115778696 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | FAM63B | GRCh38.p7 | 15:58775637 | TTCTCCCAATGATGA[A/C]TATAAGAAGTGAAGA | 54629 |
rs115831537 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAM63B | GRCh38.p7 | 15:58775278 | CATAGATGAAAGTTA[C/T]TGGGGGTCCTCAATC | 54629 |
rs115891724 | snp | C/T | 0.160609 | 0.233472 | intron-variant | FAM63B | GRCh38.p7 | 15:58849576 | AGTCCAGATAAGGTG[C/T]TGAGATTGTTATCTG | 54629 |
rs115892990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58776624 | TGAAAAGTCAGGATA[A/G]CATGGAATCCTCAGT | 54629 |
rs115894252 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAM63B | GRCh38.p7 | 15:58834462 | GTATGCTAAAACTGT[A/G]TGGGAGGCTTTTTTA | 54629 |
rs115943181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58812551 | TATCAAAACCAGGAA[A/G]TTGACATTAGTAAAG | 54629 |
rs116116698 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FAM63B | GRCh38.p7 | 15:58787378 | TGTTTTTAAGCTTTG[C/T]ATTACTTTTAATAGC | 54629 |
rs116134859 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | FAM63B | GRCh38.p7 | 15:58819465 | CCACTGCACTCCAGC[A/G]TGGGTGACAGAGCGT | 54629 |
rs116292580 | snp | A/G | 0.0263992 | 0.111815 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861578 | ATTTCTGTGAAATAA[A/G]TTTGTTTTAAATACT | 54629 |
rs116319400 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770755 | GCCGTCGAGTAGATA[C/T]GCCTGCTTTAAAATC | 54629 |
rs116409725 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58775014 | GAAGAGATGGATAAG[C/T]GAAGCAAAGTAGAGC | 54629 |
rs116411705 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | FAM63B | GRCh38.p7 | 15:58822897 | TCTCAGACACACAAT[A/T]ATTTTACATAAGATA | 54629 |
rs116522636 | snp | C/T | 0.144296 | 0.226554 | intron-variant | FAM63B | GRCh38.p7 | 15:58853369 | CCATTAAAATAAGTA[C/T]AAAATTTCTATTTCT | 54629 |
rs116536795 | snp | A/T | 0.0696718 | 0.173152 | intron-variant | FAM63B | GRCh38.p7 | 15:58823573 | GGGAGGCTGAGGCTG[A/T]AAGATCACTTGAGCC | 54629 |
rs116574240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58779809 | AATACCGCCAGTAGG[A/G]GTTGCCCTCTAATAG | 54629 |
rs116777606 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAM63B | GRCh38.p7 | 15:58813869 | GCACTTAATGTTGTC[A/C]CTATTTTTTATTTTA | 54629 |
rs116803237 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58827826 | GTGATATGGCCAGTG[C/G]GATGCCCTCAAGTTG | 54629 |
rs116840420 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58852287 | AGCAAGACTCCTTCT[A/C]AAAAAAAAAAAAAAA | 54629 |
rs116905204 | snp | C/T | 0.133777 | 0.221342 | intron-variant | FAM63B | GRCh38.p7 | 15:58805956 | GGCACGTACTGTGGT[C/T]CCAGCTACTCGAGAG | 54629 |
rs116990761 | snp | C/T | 0.00892415 | 0.0662 | missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772221 | ATCCTCAATGTTTTG[C/T]TCCTGGCCTGGAAGG | 54629 |
rs117015397 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | FAM63B | GRCh38.p7 | 15:58831267 | TACTTTTAGTTTTAA[A/G]GCAAGAATTGAGAAG | 54629 |
rs117093482 | snp | G/T | 0.0142736 | 0.0832652 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855449 | AGGCTTTGTAAATAT[G/T]GGGATGTAGAAAAGC | 54629 |
rs117140028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58776908 | AGATGAAAATTGAAG[C/T]CTCATATTTTTCAGT | 54629 |
rs117167262 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58801516 | ATTAAAATTGTGATC[A/C]ATATTTTTAAAAGGT | 54629 |
rs117199150 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58813844 | ATCCAGTTTCTCTGC[A/G]TCTTCATCAGCACTT | 54629 |
rs117258318 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58794753 | CAAGACAGAGCCAAA[A/T]ACTCAGATAATAAGG | 54629 |
rs117320945 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772519 | AGAGCATCTTAAATC[G/T]TATGATTATTTTAAA | 54629 |
rs117365676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58817175 | AAACAGAATGTAAAA[C/G]CAAGCCACAGAGTAG | 54629 |
rs117444165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58836384 | TATGGATGGTTTGTT[C/G]AAACCAGGATCTAAT | 54629 |
rs117453891 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861036 | GCTACAAAACAGTCA[A/G]CAAAAGGAATCATGT | 54629 |
rs117737052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58831182 | TTGGAGGAGATTAGC[A/G]TAAAAATGGCATAAA | 54629 |
rs117805146 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58813162 | TGAGTAGTATTTTGT[G/T]GTGTGGACCTACCGC | 54629 |
rs117806482 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58823315 | TTTTAGTAGAGATGG[A/G]ATTTTGTCATGTTGG | 54629 |
rs117829424 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772577 | CCTTATCACATATGC[A/G]AAAAAGTGAAGAATT | 54629 |
rs117830580 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FAM63B | GRCh38.p7 | 15:58825745 | CAGGTAGCTGGGACT[A/G]CAGGCTCACGCCACC | 54629 |
rs117942397 | snp | A/G | 0.000150995 | 0.00868763 | missense, nc-transcript-variant | FAM63B | GRCh38.p7 | 15:58851823 | AGAGCCAAGAGATCA[A/G]TTGGGAACAAATCCC | 54629 |
rs118015368 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58830794 | CTTGTTTACAGTATG[C/T]GAGAGAGCTGAAGCA | 54629 |
rs118075084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58850174 | ATATTAAGTTAATGC[C/T]TGACCAAAATGCACT | 54629 |
rs118107890 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FAM63B | GRCh38.p7 | 15:58848465 | GAATATTTAATTCTC[C/T]GGGTGCGGTGGCTCA | 54629 |
rs137925229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58819681 | GTGGATTTCTTAGAA[C/T]TGAAAATTCAGATTA | 54629 |
rs137926161 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857299 | AGTACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 54629 |
rs137960970 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58823051 | CATTACTTAATTATC[C/T]AGAAGTTTAACACAT | 54629 |
rs138011425 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58827090 | ATGCTACGTAGGTGA[C/T]ATTGTGTCTTTCCCA | 54629 |
rs138045194 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | FAM63B | GRCh38.p7 | 15:58794062 | CGTGTTGACGAAAGA[A/T]TCTAGGGTATGTTGC | 54629 |
rs138045792 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58854088 | TCTCTACTAAAAATA[C/G]AAAAAGTTAGCCAGG | 54629 |
rs138093111 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58775086 | ATTTTTATGATAATA[C/T]TAAGATGTTATTTGC | 54629 |
rs138120213 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58831505 | AACCTGCATGAAATC[A/C]TTTGTAATAGTAGGT | 54629 |
rs138192185 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58800658 | TTTTTCTGCATCCAG[C/T]TTAGCTTTTTTTTTT | 54629 |
rs138198263 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAM63B | GRCh38.p7 | 15:58841890 | AGAAACAGACTCATT[G/T]AAGTCAGTTTTGCTT | 54629 |
rs138205629 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58780170 | AGCACTTTGTGAGGC[A/C]GAGGCAGGCGGATCA | 54629 |
rs138214495 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772399 | GAAGGAATATTCCTT[C/T]ATACATATATCGAAA | 54629 |
rs138292699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58804918 | GGATTACTTGAGCCT[A/G]GGAGTTCAAGACCAA | 54629 |
rs138320718 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58786582 | ATCACTATAACGTAT[C/T]TTTACTTTTAACCTT | 54629 |
rs138326345 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860191 | GAAAGAATGCCTCAT[A/G]AATTAGAGAAGGACA | 54629 |
rs138365113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58808279 | TATATTCTGTGGATT[C/T]TGAAAAATGTATAAT | 54629 |
rs138488325 | in-del | -/TT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58798459 | GCAGTAAAAAAAAAT[-/TT]TTTTTTTTTTTTTGA | 54629 |
rs138492822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58814688 | TTTCCCCATTTTTTT[A/T]ATTTGGCTATGTGTC | 54629 |
rs138507891 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAM63B | GRCh38.p7 | 15:58853611 | GGATCTCGAGGCCAG[A/G]AGTTCGAGACCAGCC | 54629 |
rs138558672 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58858937 | TCTTTAAATATGTGA[A/G]GGATGCTCTTTTTGA | 54629 |
rs138588306 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58849398 | TAGTCTCAGCTACTC[A/G]GGAGACTGAGGCAGG | 54629 |
rs138589240 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58811385 | CTGGCAGGAAGTAGA[C/T]GACACACTGAAGGAT | 54629 |
rs138620929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58793770 | CTCTTGAGTGCTTCT[A/G]TTTTCTCAATGAAAT | 54629 |
rs138666892 | in-del | -/ATTA | 0.0715223 | 0.175059 | intron-variant | FAM63B | GRCh38.p7 | 15:58835209 | ATTACACAAATAATT[-/ATTA]ATTTATTTCTATTGA | 54629 |
rs138675145 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771244 | AGCGGTAGCGCGCGC[C/T]CGCGCGCGTTCTTAG | 54629 |
rs138676952 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58842976 | GAAAGTGCTTTTTTG[A/G]ATAAGACTACATTTG | 54629 |
rs138735271 | in-del | -/ACAA | 0.00557542 | 0.0525036 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860759 | GCAACATGTTTTAAG[-/ACAA]ACAGTATTTAATCCT | 54629 |
rs138790473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58837934 | TGATCATGCCACTGC[A/G]CTCCAACCTGGATGA | 54629 |
rs138790849 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58811039 | AGCTGAGCTGACACC[A/G]TGTGGTTCAAGGGAT | 54629 |
rs138834142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58800255 | TCTTAATTCTTTCCT[G/T]GAAATTTTTTCTCTT | 54629 |
rs138857645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772652 | GGACTAAGTTTTCAT[A/G]GTTATATTTAGTTTG | 54629 |
rs138864128 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | FAM63B | GRCh38.p7 | 15:58836066 | AGGCGCCCGCCACCA[C/T]ACCCAGCTAATTTTT | 54629 |
rs138908932 | snp | A/G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58830852 | CTCAGCTGGGAATGT[A/G/T]CACATTGGGCCACTC | 54629 |
rs138910104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58775756 | GGAAAGTTGATGCCA[A/G]AGTTTGGTTGTGTTG | 54629 |
rs138935754 | in-del | -/ATT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840670 | ATTATTATTATTATT[-/ATT]TTGAGATGGAGTCTT | 54629 |
rs138974288 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58797997 | CATCTGGGCACCTTC[C/T]ATGATTTAAAGTATG | 54629 |
rs139055514 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58827254 | ATATTATTCTTTGAA[A/C]TGTGTGAATATGCTA | 54629 |
rs139080301 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58782148 | TATTTTGAAAAAAGC[A/C/G]GGTAAAGCTTCTCTT | 54629 |
rs139197611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58788236 | CAATAAATTGTAGAA[G/T]GGGAGATGGTACAGA | 54629 |
rs139244151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58785385 | ATCATCTAATGCAGA[C/G]ATCAGCAAACTTTTT | 54629 |
rs139271721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58821267 | GGAATAATTTTATTA[A/G]TCCTATAAATTAACA | 54629 |
rs139323009 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58815400 | GTGTCACCCAGGCTG[A/G]AGTGCAGTGGCACAG | 54629 |
rs139323881 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAM63B | GRCh38.p7 | 15:58816701 | GCAATCCTTTAAACA[A/G]AAGGTTCTAAGACAA | 54629 |
rs139344617 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FAM63B | GRCh38.p7 | 15:58862199 | GCCATGATCATGTCA[C/T]TGCAGTCTAGCCTGA | 54629 |
rs139391025 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58818705 | GCTACCCAGGTGTGA[C/T]CTCGGCTCACTGCAA | 54629 |
rs139398988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58809374 | GCATGATGTCCTCAA[A/G]GTTCATCTGGTTGTA | 54629 |
rs139402598 | snp | C/G | 0.00999612 | 0.0699867 | missense, nc-transcript-variant | FAM63B | GRCh38.p7 | 15:58847426 | CTTCGACCTCCTTCA[C/G]ATCCTGAAACTGTAT | 54629 |
rs139405416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58809523 | TAATGTTGCAATGAG[C/T]GTGGGTGTACAACTA | 54629 |
rs139431306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58773122 | TTATATCTGTAGATG[C/T]AATGTTTCCTAGGAA | 54629 |
rs139471307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58811982 | AAATTTCAAAATAAT[A/G]TTAGTTAATTGTAAA | 54629 |
rs139473342 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58773422 | AATAAAATTAGAAAC[C/T]TTGCCATTGTCTGGT | 54629 |
rs139512673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58812543 | TAGTAAAATATCAAA[A/G]CCAGGAAATTGACAT | 54629 |
rs139620455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58817408 | ACCACTGTACATACA[A/T]CAGACTGGCTAACAT | 54629 |
rs139651928 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58836112 | AGACAGGGTTTCGCT[C/G]TGTTAGCCAGGATGG | 54629 |
rs139652880 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | FAM63B | GRCh38.p7 | 15:58799306 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 54629 |
rs139712130 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAM63B | GRCh38.p7 | 15:58850216 | AAACTAATCTGAGTG[C/T]GTACATGGGAGGAGG | 54629 |
rs139752706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58833121 | TCAGAAGTTTGTCAA[C/T]TTATACATAGATTTC | 54629 |
rs139829371 | snp | A/G | 0.300926 | 0.244758 | intron-variant | FAM63B | GRCh38.p7 | 15:58795608 | ACAGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 54629 |
rs139839213 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855407 | GACAATGTGATTGAG[C/T]GTATGGAGGAAAGCA | 54629 |
rs139895318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58798520 | TAGTGCAATGGCACA[A/G]TCTTGGCTCACTGCA | 54629 |
rs139898373 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58796042 | GACCTTCATCAAACC[C/G/T]TGTCACTGCAGTGAT | 54629 |
rs139910584 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856090 | TGTGTTTCTATATAT[A/G]GTTTGGAAAACTATC | 54629 |
rs139986422 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58839180 | ATTCTAGAGATGTTT[A/G/T]AGCTGTGGGCTTTGA | 54629 |
rs139987320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58851035 | CTGGAGCGCAGTGGC[A/G]TGATCTCAGCTCACT | 54629 |
rs140147267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58832459 | GTGTCAAACTCCTGA[C/G]CTCAGGTGATCGCCC | 54629 |
rs140216331 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857026 | GATAAGTAGATGTCA[A/G]TGTATACTTACAAGG | 54629 |
rs140252358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58774802 | CTTGGAACCTTCAAC[A/C]TTGGTTGAAGTGTGC | 54629 |
rs140258696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58778044 | TTTATGAAGTTAAGC[A/C]AGAAGGTATATAACA | 54629 |
rs140269564 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FAM63B | GRCh38.p7 | 15:58837693 | CATATTTAATGACCA[G/T]CCAGGCTTACACATG | 54629 |
rs140345884 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58826707 | TATTATTTAATATAT[C/T]GTTCATATCAGAATT | 54629 |
rs140392641 | snp | A/T | 0.00677751 | 0.0578171 | intron-variant | FAM63B | GRCh38.p7 | 15:58810191 | TTTGTTCTCGTTTTG[A/T]TGTTTCTGAATTAGA | 54629 |
rs140421070 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58779950 | TGGGCCCAGGTGGTA[C/G]TAGCAATCATAGGGG | 54629 |
rs140472882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58841135 | TATAGGCGCGCACCA[C/T]CATGTCCAGCTAATT | 54629 |
rs140493823 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58814186 | TTCAGGTGATCCACC[C/G]GCTTCGGCCTCCCAG | 54629 |
rs140521149 | in-del | -/TATATATATATATATATA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58791216 | TCAGGAAAGCAATTT[-/TATATATATATATATATA]TATATATATATATAT | 54629 |
rs140537036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58807808 | TACAACTTTTCACTT[C/T]TATTTTGTCCCAGCC | 54629 |
rs140538841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58844089 | AGTCTTAAGAAAGCA[C/T]TGACTGCATAATCTA | 54629 |
rs140590218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58794474 | GAGACATCTCCATAC[A/G]TATTGAAATTACCAA | 54629 |
rs140662697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58824300 | AAACTATAGTTAATA[C/T]ATGTGTTATTGATAA | 54629 |
rs140711522 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58796878 | TGTATTTCTGACCCT[A/G]TTTCCTATCCAGCTC | 54629 |
rs140726836 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58792243 | TTAAACAGAATTACC[A/G]TATGACCATGAAATA | 54629 |
rs140747821 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58852148 | AAAATTAGCCGGGCG[G/T]GGTGGTGGTGAACAC | 54629 |
rs140803554 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58821566 | AACTTGGAAACTGTT[C/G]GGTGTTGATTTTAGT | 54629 |
rs140814279 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FAM63B | GRCh38.p7 | 15:58807643 | GCTGGGATTACAGGC[A/G]TGAGCCATTGCGCCC | 54629 |
rs140827713 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAM63B | GRCh38.p7 | 15:58829504 | TGAGAAAGACCTTTC[C/T]AATGTTGAATTTTTG | 54629 |
rs140829555 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | FAM63B | GRCh38.p7 | 15:58793673 | AAATTAGCCTTAGAT[A/C]GTTCATCCATGGTAA | 54629 |
rs140855892 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58857402 | AGCCAGGCATGGTGG[C/T]GGGCACCTGTCATCC | 54629 |
rs140887489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58840386 | TGGAAAAATACCTCT[C/G]TGTTTCTTTCATTAT | 54629 |
rs140984439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58785260 | CACTTTTTAGTTTTA[A/G]TAAACATCCAAAGTA | 54629 |
rs140985962 | in-del | -/A | 0.0532157 | 0.154195 | intron-variant | FAM63B | GRCh38.p7 | 15:58776859 | GACCCCCATCTCTGT[-/A]AAAAAAAAATTATAA | 54629 |
rs140997149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58844797 | TGGTGTGCTCCTATA[A/G]TTGCAGCTACTTGGG | 54629 |
rs141001045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58777539 | AGCACTTTGGGAGGC[C/T]GAGGCCAGAGGATCA | 54629 |
rs141108876 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58779804 | GTATAAATACCGCCA[A/G]TAGGAGTTGCCCTCT | 54629 |
rs141131113 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAM63B | GRCh38.p7 | 15:58781918 | AAAAAGAAAAAAAAA[A/G]GAAAGAAATACTGAT | 54629 |
rs141192808 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58810603 | GGGCCCAACTACAAG[A/G]TTAGAGGGAAGAGCT | 54629 |
rs141207115 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58815999 | CTATTATTTCTTTAC[C/G]TGGTTAACTGTCATC | 54629 |
rs141230922 | snp | A/C/G | 3.31746e-05 | 0.00407262 | missense, nc-transcript-variant | FAM63B | GRCh38.p7 | 15:58847435 | CCTTCAGATCCTGAA[A/C/G]CTGTATACAAAGGAC | 54629 |
rs141249924 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAM63B | GRCh38.p7 | 15:58775614 | AATGTAGCGTTCCCA[A/G]TGATGACTTCTCCCA | 54629 |
rs141253800 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58813687 | AAGTGATCCTCTTGC[C/T]GCAGCCTCCCAAGTA | 54629 |
rs141302936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58854425 | CCTTTCTAGATAACC[A/G]TGAGTAAGTCCCTCA | 54629 |
rs141370138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58803614 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCTGTTCA | 54629 |
rs141417069 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAM63B | GRCh38.p7 | 15:58826022 | TATGTGCCATAGACA[C/T]TGAACATTATAGTTT | 54629 |
rs141503750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58808966 | TCTGTAATCCCAATA[C/T]GTTGAGAGGCTGAGG | 54629 |
rs141619774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58812310 | GGTGCAGTGGCAGGC[A/G]CCTGTAATCCTAGCT | 54629 |
rs141643053 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58853712 | GTAGTCCCAGCTACT[C/T]GGGAGACTTGAGGCA | 54629 |
rs141647232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58793883 | GAGAAATGGGAGATT[A/G]AATGGATTAGAGAGC | 54629 |
rs141693873 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58846273 | ATTTACCCTCATGTG[A/T]TTATTATGCATTGCA | 54629 |
rs141716234 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAM63B | GRCh38.p7 | 15:58845564 | AATGTTGGTGAGGAT[A/G]TGGAGAAAAGGGAAC | 54629 |
rs141718392 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | FAM63B | GRCh38.p7 | 15:58785793 | GCAATTCTCCTGCCT[C/T]AGTCTCCCAAGTAGC | 54629 |
rs141750601 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58797737 | CTTCCCTGCTCGTTA[G/T]CACTAGCACTCTACT | 54629 |
rs141790910 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAM63B | GRCh38.p7 | 15:58789024 | CTCAAAAACAAAAAC[A/G]TATTTTATTTTTAAA | 54629 |
rs141802618 | in-del | -/TATATATATATATATATATA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58791216 | TCAGGAAAGCAATTT[-/TATATATATATATATATATA]TATATATATATATAT | 54629 |
rs141822769 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAM63B | GRCh38.p7 | 15:58835920 | TTTTGTTTTGTTTTG[C/T]TTTGTTTTTGAGATG | 54629 |
rs141918761 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | FAM63B | GRCh38.p7 | 15:58804711 | ACTTGGGAGGCTGAG[C/G]TCAGAGGATCGCTTG | 54629 |
rs141927707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58777140 | TTAAAAACTATTAGC[A/G]TATCAGTTTTGCTTT | 54629 |
rs141936552 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58838798 | GTTGTCCAGACTGGT[A/C/T]TCAAATCCCTGACAT | 54629 |
rs142041285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58838136 | GGTGTGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 54629 |
rs142062754 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58774221 | GGCGCGGTGGCTCAC[A/G]CCTGTATTCCCAGCA | 54629 |
rs142135542 | snp | A/G | | | intron-variant | FAM63B | GRCh38.p7 | 15:58830636 | ACATGTATTTTCTCT[A/G]TAAGGCACATCACAG | 54629 |
rs142154092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58809939 | CGCATGCCACCATGC[C/T]CAGCTAATTTTTGTA | 54629 |
rs142173154 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772783 | CTGAGACCCAATTAC[C/T]GTAACTTCTTGGTTT | 54629 |
rs142187175 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58836084 | CCAGCTAATTTTTTT[C/G]TATTTTTAGTAGAGA | 54629 |
rs142200512 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58834324 | TTAATCCCTGTTTGG[A/C]AAGGTCTTCTCATTC | 54629 |
rs142204511 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770080 | AAAAAAGACAGTAAG[C/T]TCCATGAAGATATAA | 54629 |
rs142262354 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58813728 | CAGGCATGCACCATT[A/G]TGCCCCGTTAACTTG | 54629 |
rs142303662 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861527 | TTTTTGCATAAAGAT[A/G]CCTAAAACCATCTAC | 54629 |
rs142323296 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58790016 | ACTCCTGGGCTCAAG[C/T]GATCCTCCCACCTTG | 54629 |
rs142359441 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAM63B | GRCh38.p7 | 15:58848471 | TTAATTCTCCGGGTG[C/T]GGTGGCTCACACCTG | 54629 |
rs142425188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58799126 | AAGAATGATGTAGGC[A/G]AAGAAATTCTGAAGG | 54629 |
rs142467456 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAM63B | GRCh38.p7 | 15:58787079 | ACGTGATCCGCCTGC[A/G]TTGGCCTTCCAAAGT | 54629 |
rs142500342 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAM63B | GRCh38.p7 | 15:58836952 | AAGGGTCAAAAGCAC[A/G]TCTTCTTCACTGACC | 54629 |
rs142500735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58814920 | AGTGCCGAGGTTACA[A/G]ATGTGAGCCACTGTG | 54629 |
rs142533607 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58802931 | GCGGAGCTTCATTTT[A/C]TTCAGTATTCTTCCT | 54629 |
rs142564243 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58818370 | CTTAAGCAATCCTGT[A/C]TCAGCTTCCTGAGTA | 54629 |
rs142607472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58779341 | AAAGTGAGGCACCAT[A/G]AAGGTGAGCCTCTTG | 54629 |
rs142611089 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | FAM63B | GRCh38.p7 | 15:58820037 | TTGGGAGACTGAGGC[A/C]GGCAGAGTACTTGAG | 54629 |
rs142614543 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840271 | AACAATGATTTTTAT[C/T]GCACAGGACATTTTC | 54629 |
rs142640909 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | FAM63B | GRCh38.p7 | 15:58848801 | CTTTCTAGGACTTTT[A/C]TTTGAAAAACAGTTC | 54629 |
rs142692789 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58791923 | TGGGGAAGGAGAAAG[A/G]GCCGGCACGGTCAGC | 54629 |
rs142719663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58845961 | AGAAAGACACACTTC[A/G]CATGTTCTTTCTTAT | 54629 |
rs142732750 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772464 | GTTTAAGAGTTCAAC[A/G]TTCAATTGTGGTTGA | 54629 |
rs142866311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58808479 | TGTAGCCTTTTCATA[G/T]TAGCTTGTTTTCTTT | 54629 |
rs142878356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58818143 | TTTGCTTTTACTCTA[A/G]AATATAAGCTTTATG | 54629 |
rs142904808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58798022 | AGTATGCTGAAAAGC[C/T]CATATGCTCAAAAAT | 54629 |
rs142945089 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58828201 | TCTTTTCAAGTAAAA[A/T]CTGGGCATTTGTCAT | 54629 |
rs142951474 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856864 | ATCTGTTTATTGCCC[A/G]TGGAAAATATATGTG | 54629 |
rs142952633 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAM63B | GRCh38.p7 | 15:58833209 | AGTAGCACTTCATGC[A/G]TGGGGATAAAAATAC | 54629 |
rs142972693 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | FAM63B | GRCh38.p7 | 15:58816981 | CAAACATGGAGGGGG[-/A]AAAAAAAGTTTAACT | 54629 |
rs142984787 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58827334 | CTGAATCAGTTATTA[C/G]TGTGGTGGTTATAAT | 54629 |
rs143003293 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58805365 | GAAAGACCAACACAG[A/C]GCTGCAATATTCCCA | 54629 |
rs143056967 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58830969 | AGTTAGATGAACTTG[C/T]AGATATGAACTTGCA | 54629 |
rs143057018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58794804 | GTTGAATACCTAGGG[A/G]ATTTGCTAATGGCAG | 54629 |
rs143093190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58849294 | GATCACGAGGTCGGG[A/T]GATCAAGACCATCCT | 54629 |
rs143159323 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58804587 | CCAAAGCAGGCGGAT[A/T]GCTTGAGCCCAGTAG | 54629 |
rs143283504 | in-del | -/G | 0.0217236 | 0.101931 | upstream-variant-2KB, intron-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58770338 | TGAAAGAAAAAAGAT[-/G]GGGGGAAAAAGCCCT | 54629 |
rs143320689 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAM63B | GRCh38.p7 | 15:58842582 | ATTTGGAAACTGGAA[C/T]AAGGAAAGTGATGAT | 54629 |
rs143337859 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58842235 | ATATTCAGTCCCAAC[A/G]TTTTTGAGGTTGGTT | 54629 |
rs143350858 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | FAM63B | GRCh38.p7 | 15:58847088 | ATTTCTTGTTATAGT[G/T]TAGTGTGCCAATTAT | 54629 |
rs143359138 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | FAM63B | GRCh38.p7 | 15:58787529 | GATCAGAAGGTTAGG[A/C]GATTGAGACCATCCT | 54629 |
rs143405176 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAM63B | GRCh38.p7 | 15:58793127 | GCTAATGGGTACAGG[A/G]TTTCTTTTAGGGAAG | 54629 |
rs143469071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58777717 | TTATTACATTTAATT[C/T]GAGCTCAAATTTGTA | 54629 |
rs143472477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58830432 | AAACACCAACATGAC[A/G]CTCACAGGAAATGCT | 54629 |
rs143488084 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58782749 | GATCTCACTTCTCAT[A/C]ACAGTACTTCTACTT | 54629 |
rs143498226 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58843947 | TTACAAATTGTGACA[A/G]TATTGACATTTATAT | 54629 |
rs143504796 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58797572 | TTAATGTGGCTGCTA[C/G]AAAATTTAAAATTAC | 54629 |
rs143550992 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58841407 | TTTTCCTTTCTTTTC[-/T]CTTTTTTTTTTTTTT | 54629 |
rs143579200 | snp | A/G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58835512 | ACAAAAATTAGCTGG[A/G/T]CATGGTGGTGGGTGC | 54629 |
rs143583599 | snp | C/G/T | 0.000840866 | 0.0204875 | missense, upstream-variant-2KB, nc-transcript-variant | FAM63B, LOC101928725 | GRCh38.p7 | 15:58771613 | CTCCCGCGGGCTCTC[C/G/T]TGAGGTTCCCGGACC | 54629 |
rs143584135 | snp | A/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58845571 | GTGAGGATATGGAGA[A/T]AAGGGAACCCTTATA | 54629 |
rs143644047 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FAM63B | GRCh38.p7 | 15:58784104 | GCTGAGGTAGGAGGA[C/T]TGCTTGAGGCCAGGA | 54629 |
rs143687955 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58776170 | CATAGAGTAAATATG[A/G]TAGTACTACATAGAG | 54629 |
rs143732528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58827091 | TGCTACGTAGGTGAC[A/G]TTGTGTCTTTCCCAG | 54629 |
rs143811940 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860294 | TCAGGAAACTGGCCC[A/G]GTGCGGTGGCTCATG | 54629 |
rs143827884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58822104 | AAAATACAACAAAAA[A/G]TTAGTTGGCCATGGT | 54629 |
rs144098473 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58811837 | AAGGAAAAAATAATT[C/G]TACTGTAACATACTA | 54629 |
rs144120787 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58782468 | AAGCAGACATCATTT[A/T]CTTCTACAAACTTAA | 54629 |
rs144129685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58847706 | AGTTTGAATTTTATT[C/T]TAATTGCAGTAGGAA | 54629 |
rs144162720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58813574 | TGCAGTTGGTGGGTT[A/G]TATCATAGTTGCTTG | 54629 |
rs144177219 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58794304 | GTAATAATGAAACTG[A/T]ATTACCATGGGAAAT | 54629 |
rs144228032 | in-del | -/TTT | 0.0205511 | 0.0992634 | intron-variant | FAM63B | GRCh38.p7 | 15:58800418 | AAGATCCCTGTGATC[-/TTT]TATAGTCAGCCAAAC | 54629 |
rs144303943 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58798665 | TTCATCATCTTGGCC[A/G]GGCTGGATTCAAACT | 54629 |
rs144330063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58803341 | GGCATGGTGATGCGC[A/G]CCTGTAGTCCCAGCT | 54629 |
rs144371197 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58836722 | CTCCTGGGTTCAAGC[G/T]ATCCTCATGGCTCAG | 54629 |
rs144375553 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FAM63B | GRCh38.p7 | 15:58773285 | GTGAGACCCTATATT[A/G]AAAGAAAAAGAAAAA | 54629 |
rs144383107 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58801800 | ACCCGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 54629 |
rs144441185 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58786860 | TTGAGATGGAGTTTC[A/G]CTCTTGTCACCCAGG | 54629 |
rs144446890 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58845972 | CTTCGCATGTTCTTT[C/G]TTATTTTTGCGGGCT | 54629 |
rs144465855 | in-del | -/TGATCCT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58814616 | CTCCTGGGCTCAAAC[-/TGATCCT]CCTCCTCAGCCTCCC | 54629 |
rs144528494 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58799369 | TCGGGAGATCGAGAC[C/T]ATCCTGGCTAACACA | 54629 |
rs144542465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58791514 | CCCAGCTACTTGGGA[C/T]GCTCAGGTGGGAGGA | 54629 |
rs144554051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58813223 | TTTCCCGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 54629 |
rs144566192 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAM63B | GRCh38.p7 | 15:58815506 | AGGTGCACACCAGCA[C/T]GCCTGGCAATTTTTG | 54629 |
rs144602888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58793753 | ATGTGGTTGCAGCGC[A/G]TCTCTTGAGTGCTTC | 54629 |
rs144634000 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58823257 | ATTCTCCTTCCTCAG[C/T]CTCCTGAGTAGCTGG | 54629 |
rs144639525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58823910 | CAAGCTCTCATTACC[A/G]TAGATAATTACTAAA | 54629 |
rs144676578 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58821592 | TTAGTGCTGATTTTG[G/T]TTTTCGTAAATAATA | 54629 |
rs144706813 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58826490 | CGCCTTGGCCTTCCA[A/G]AGTGCTGGTATTACA | 54629 |
rs144740074 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58788886 | GCGTGGTGTCATGCA[C/G]CTATAGTCCCAACTA | 54629 |
rs144745969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58825012 | TGTTCAGTTAAAGTA[A/G]TCTGCTTTCATTTTC | 54629 |
rs144746841 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58790368 | TTTTGAGGAATAGCC[-/A]ATATGACTGTCAAGG | 54629 |
rs144781721 | in-del | -/ACTTT | 0.0170251 | 0.090679 | intron-variant | FAM63B | GRCh38.p7 | 15:58833247 | GTTCTATTTGCCAAC[-/ACTTT]ACTTCAGCCAAAATG | 54629 |
rs144826086 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FAM63B | GRCh38.p7 | 15:58805889 | GACCATGCTGGCTAA[C/T]ACAGTGAAACCCCAT | 54629 |
rs144840164 | in-del | -/C | 0.0700422 | 0.173537 | intron-variant | FAM63B | GRCh38.p7 | 15:58805252 | GCTTATATGGCTGGG[-/C]TGAGTCTAAGCTAAT | 54629 |
rs144911267 | in-del | -/AAAAG | 0.409041 | 0.192888 | intron-variant | FAM63B | GRCh38.p7 | 15:58785161 | AAAAAAAAAAAAGAA[-/AAAAG]AAGCAAGCTTTTGGG | 54629 |
rs144929323 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAM63B | GRCh38.p7 | 15:58809810 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGACCAGG | 54629 |
rs144964036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58775696 | ATAGAGATTGGCTGG[A/C]TCTTTCCAAAGATAG | 54629 |
rs144977422 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58837797 | GAAGTAAGACCTTGT[C/T]TGTACAAAAAACTTT | 54629 |
rs145012731 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | FAM63B | GRCh38.p7 | 15:58773701 | ATCTTTTTTTTTTTC[A/G]TTTGTTTGTTTGTTT | 54629 |
rs145022159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58779904 | CACTCCCCATTCAAC[A/C]TTGTCTGTTGAGTCC | 54629 |
rs145068471 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58837734 | ACTTTGAGAGGCAGA[C/G]GTGGGAAGATCACTT | 54629 |
rs145088792 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58806346 | ACAGGCGTGAGTCAA[C/T]GTGCCAACTTTTTTT | 54629 |
rs145185046 | in-del | -/TTA | | | intron-variant | FAM63B | GRCh38.p7 | 15:58840629 | TCACTATTTATTTAC[-/TTA]TTATTATTATTATTA | 54629 |
rs145197702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58847901 | GCACATATCTGAGCT[A/G]TATTTTGACTAGTTA | 54629 |
rs145198641 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAM63B | GRCh38.p7 | 15:58788339 | TAGAGCAGTGCTACC[A/G]AAAGTGTGATTCATG | 54629 |
rs145239339 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58822817 | AGGCTATAATTCTTC[C/T]GTCTGTGAAAGGGAA | 54629 |
rs145256093 | in-del | -/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58809411 | CAGGATTTCTTTCTT[-/T]TTTTTTAAGGCTGAA | 54629 |
rs145337947 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58821464 | GAAATAAAGTTGCAT[G/T]TAATAATCCCATTTA | 54629 |
rs145358661 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAM63B | GRCh38.p7 | 15:58792467 | AAAAATTAGCCGGGC[A/G]TGGTGGCACATGCCT | 54629 |
rs145433608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58826008 | TATTGAGCCTTTATT[A/G]TGTGCCATAGACACT | 54629 |
rs145520941 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAM63B | GRCh38.p7 | 15:58810460 | GGCAAATTAATCTCA[A/G]TTTATATTTTTTGTT | 54629 |
rs145534040 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58829738 | GTATTCAATGAATTT[C/G]TTTTGGCTGTAGACC | 54629 |
rs145608736 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | FAM63B | GRCh38.p7 | 15:58807652 | ACAGGCGTGAGCCAT[C/T]GCGCCCGGCCTAAAA | 54629 |
rs145635567 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAM63B | GRCh38.p7 | 15:58807879 | TCGTTTTTGCACTGG[A/C]ATCTACTTTGGAATG | 54629 |
rs145725651 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58841300 | CTTCATGATTTTCTT[A/G]TAAATAATTTCAATT | 54629 |
rs145829831 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58800165 | CTCTCTTCCATTTTT[G/T]TGGCCTAAAGTAGCT | 54629 |
rs145856729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58797076 | GAGTCCTTGAAATGT[C/G]GCCAGTGTGAATTGA | 54629 |
rs145886213 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856534 | TAAATCATCAAAGAA[C/T]CTGTTTGGGATATAA | 54629 |
rs145953146 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58834751 | CGTGAATTACATCTT[C/T]ATATTTTCTTCAACA | 54629 |
rs145955493 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58787228 | CCAACTCCTGACCTC[A/G]AGTGATCTGCCCACC | 54629 |
rs145997079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58820134 | AGTTGGGCATGGTGG[C/T]GTGCACCTGTAGTCT | 54629 |
rs146039047 | snp | C/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58817078 | ATTTCAAAAACAAGA[C/T]ACAAACCTATTAACT | 54629 |
rs146095579 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | FAM63B, LOC101928725 | GRCh38.p7 | 15:58772470 | GAGTTCAACATTCAA[C/T]TGTGGTTGATACACT | 54629 |
rs146121173 | snp | G/T | | | intron-variant | FAM63B | GRCh38.p7 | 15:58805850 | GGAGGCTGAGGCGGG[G/T]GGATCACAAGGTCTG | 54629 |
rs146160969 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAM63B | GRCh38.p7 | 15:58801801 | CCCGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 54629 |
rs146205499 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58816401 | TTTTTATTTTTAATT[A/C]TTTTTTTGTTTGCTT | 54629 |
rs146234067 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58830643 | TTTTCTCTATAAGGC[A/G]CATCACAGCCTTTGT | 54629 |
rs146246265 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | FAM63B | GRCh38.p7 | 15:58849768 | ATTTTTTGAGACAGG[G/T]TCTCACTCTGTCACC | 54629 |
rs146286327 | snp | C/T | 0.000456494 | 0.0151009 | intron-variant | FAM63B | GRCh38.p7 | 15:58847290 | TCTTTTGTTACTTCT[C/T]ATTAAGGGTCAACTG | 54629 |
rs146342147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58804757 | GGTTGCTGTGAGCCA[A/T]ATCACACCACTGCAT | 54629 |
rs146364805 | in-del | -/AT | 0.103794 | 0.20279 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58861048 | TCAGCAAAAGGAATC[-/AT]GTTTGCTTGTGAAAC | 54629 |
rs146367123 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | FAM63B | GRCh38.p7 | 15:58836095 | TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCGC | 54629 |
rs146407296 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FAM63B | GRCh38.p7 | 15:58832864 | TGGAAGTTTATATTT[A/C]AGTGCTAAAGGAATT | 54629 |
rs146468797 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58785338 | GTAAGTAAGTGAGTC[A/G]AAATATTTGTGTATT | 54629 |
rs146483138 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAM63B | GRCh38.p7 | 15:58782614 | GGTCACAAAGTTCTG[C/T]CAATTATGTTTTGTA | 54629 |
rs146508358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58813635 | AAGAGACAGGGTCTT[C/G]CTTTGTTGCCCAGGC | 54629 |
rs146522906 | in-del | -/TTA | 0.145642 | 0.227177 | intron-variant | FAM63B | GRCh38.p7 | 15:58831544 | AGTAAATGCATTTGT[-/TTA]TAAAAAAGAATTTCA | 54629 |
rs146524862 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58779664 | TTCACACAATTGTGG[A/G]GTTTTGTTTACACAA | 54629 |
rs146625148 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | FAM63B | GRCh38.p7 | 15:58799428 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGTGCCT | 54629 |
rs146672259 | snp | A/G | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58856947 | AAATGCTGCCATACT[A/G]CATTCCCTCTGGAAG | 54629 |
rs146745700 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAM63B | GRCh38.p7 | 15:58783084 | GCCACCGCGCCTGGC[C/T]AATTGTTTGTATTTT | 54629 |
rs146751052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58844061 | AAACTGATGAAATTA[A/G]AAGGAAGATTTGAGT | 54629 |
rs146752527 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAM63B | GRCh38.p7 | 15:58818450 | TTGTGAAGACAGGGC[C/T]TTGTTATGTTGCCTA | 54629 |
rs146761119 | in-del | -/GTTT | | | intron-variant | FAM63B | GRCh38.p7 | 15:58785547 | GTGTTCCAAAAAAAC[-/GTTT]ATTTAGAAAAACAGA | 54629 |
rs146789752 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58779940 | GAAGGACATTTGGGC[C/T]CAGGTGGTACTAGCA | 54629 |
rs146792926 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58841127 | GCTGGGATTATAGGC[A/G]CGCACCACCATGTCC | 54629 |
rs146822969 | in-del | -/TGTT | 0.0569829 | 0.158885 | intron-variant | FAM63B | GRCh38.p7 | 15:58825594 | TGTTTGTTTGTGTGG[-/TGTT]TGTTTGTTTGTTTGT | 54629 |
rs146873292 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58829215 | AAAATTTAAAACTAG[G/T]TTAGCCTTTTCCACT | 54629 |
rs146892249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAM63B | GRCh38.p7 | 15:58796781 | ACCTGCCTTGGCCTC[C/T]GGAAGTGCTGGGATT | 54629 |
rs146913358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58815160 | CTTTATTCATATACA[C/T]GTAGATAGCCAGTTG | 54629 |
rs147014498 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FAM63B | GRCh38.p7 | 15:58800600 | ATTCATTCTTCCCCT[C/T]AAAAGATGCTTTTTC | 54629 |
rs147027239 | in-del | -/GAAA | 0.14665 | 0.227637 | intron-variant | FAM63B | GRCh38.p7 | 15:58844945 | AAAAAAAAAAAAAAT[-/GAAA]GGACAACCCACAAAA | 54629 |
rs147083272 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FAM63B | GRCh38.p7 | 15:58789108 | TTTGGGAGGCCGAGG[C/T]GGGCCGATCACAAGG | 54629 |
rs147085482 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58848727 | CTCCAGCCTGGGCAA[A/C]AGAGCGAGACTCCAT | 54629 |
rs147118971 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58786067 | TTACTGAATAATAAA[A/T]CTACTGGATGACTAA | 54629 |
rs147123371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58845597 | TTATACACTGTTGAT[A/G]GGAATATAAATGAGT | 54629 |
rs147138307 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAM63B | GRCh38.p7 | 15:58777892 | TAAATTTATCAAAAT[A/G]TATGACTTAGAATAC | 54629 |
rs147143440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58840071 | ACTCCTGACCTCAGG[C/T]AGTCTGCCCGCCTCT | 54629 |
rs147211045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58827132 | CGGGGGCACATGAGC[C/T]TGATTATCTCATTAT | 54629 |
rs147247513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58824270 | TCTCTGACATTGATT[C/G]CTCAGGATAATGAAA | 54629 |
rs147265460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58846026 | TGGAGATAGAGAGTA[A/G]AATGATGGTTACCAG | 54629 |
rs147284759 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860298 | GAAACTGGCCCGGTG[C/T]GGTGGCTCATGCCTG | 54629 |
rs147318346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58811974 | TAAGATTCAAATTTC[A/G]AAATAATATTAGTTA | 54629 |
rs147354632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58809518 | ATGAATAATGTTGCA[A/G]TGAGCGTGGGTGTAC | 54629 |
rs147419207 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58798405 | GCTGGGACTACAGGC[A/G]TGAGCCACCACACCC | 54629 |
rs147421424 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58859823 | TTTACATGAAGGATT[A/C]TACTTTCTAATTTTA | 54629 |
rs147455446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58795075 | CAGCTGCTCGGGAGG[C/T]GGAGGCAGGAGAATA | 54629 |
rs147457610 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58855177 | ACCTTTATTTAGGAA[C/T]GTACATTTTAGGTAT | 54629 |
rs147524884 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58780451 | AAGTTTAAATAACTA[A/G]TCCAAGGTAAGATTA | 54629 |
rs147529160 | snp | C/G/T | 0.0119091 | 0.0762411 | intron-variant | FAM63B | GRCh38.p7 | 15:58842721 | TCTGTTTATGAAGCA[C/G/T]TTAGAGGCTTTGTAC | 54629 |
rs147596491 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAM63B | GRCh38.p7 | 15:58773725 | TTTGTTTTAAAGACA[A/C]ATTAGAGCAATTTAA | 54629 |
rs147601666 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAM63B | GRCh38.p7 | 15:58836971 | TCTTCACTGACCCAG[C/T]GACAGATTACCTGAT | 54629 |
rs147705138 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAM63B | GRCh38.p7 | 15:58821482 | ATAATCCCATTTAAT[C/G]TTATTTTGCATAATT | 54629 |
rs147708670 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAM63B | GRCh38.p7 | 15:58848739 | CAACAGAGCGAGACT[C/G]CATCTCAAAACAAAA | 54629 |
rs147724434 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58851561 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTAGGAC | 54629 |
rs147767896 | snp | A/T | | | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860967 | TAAATGACAGCTTGT[A/T]ACAGATTCACACATT | 54629 |
rs147805353 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAM63B | GRCh38.p7 | 15:58806095 | ACAACAAAAGAAAAG[A/G]CAAAGTCTCCCTCTG | 54629 |
rs147861805 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58835221 | ATTATTAATTTATTT[A/C]TATTGAGATACAGTT | 54629 |
rs147893567 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58788945 | TGAACTCAAGAGGTG[A/G]AGGTTACAGTGAGCC | 54629 |
rs147916342 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | FAM63B | GRCh38.p7 | 15:58850664 | TCACAGCTCACTGCA[C/G]CCTCAACTTTCTGGC | 54629 |
rs147930380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAM63B | GRCh38.p7 | 15:58821654 | TTCTAAAGAGTGATA[C/T]GGCTTTCTTTTGTTT | 54629 |
rs147989427 | in-del | -/C | 0.0640965 | 0.167152 | intron-variant | FAM63B | GRCh38.p7 | 15:58844003 | TTTAATGCATTAAAA[-/C]CCTATTCTATATTAT | 54629 |
rs148002650 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAM63B | GRCh38.p7 | 15:58797733 | ACCTCTTCCCTGCTC[A/G]TTATCACTAGCACTC | 54629 |
rs148092923 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAM63B | GRCh38.p7 | 15:58835912 | GTTTTTTGTTTTGTT[C/T]TGTTTTGTTTTGTTT | 54629 |
rs148117162 | in-del | -/A | | | intron-variant | FAM63B | GRCh38.p7 | 15:58843833 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54629 |
rs148143843 | snp | G/T | 0.021333 | 0.101051 | intron-variant | FAM63B | GRCh38.p7 | 15:58838437 | TCAGCAAACAAAATT[G/T]AACATCTAGATAGAA | 54629 |
rs148146060 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAM63B | GRCh38.p7 | 15:58776347 | TACCTCATTCTCCAG[A/G]AGACAGAGAGAAAAC | 54629 |
rs148180119 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAM63B | GRCh38.p7 | 15:58789263 | GAATGGTGTGAACCC[A/G]GGAGGCATAGCTTGC | 54629 |
rs148182231 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAM63B | GRCh38.p7 | 15:58815925 | CCTCGTGATCCGTCT[C/G]CCTCGGCCTCCCAAA | 54629 |
rs148214368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58826667 | TCACAATGCAATTAT[G/T]TCAAGCAATTTAGCA | 54629 |
rs148304397 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAM63B | GRCh38.p7 | 15:58804697 | CTATAGTCCCAGCTA[C/T]TTGGGAGGCTGAGGT | 54629 |
rs148341176 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAM63B | GRCh38.p7 | 15:58842338 | TACTCTATGTTTAGG[A/G]ATTAGAAGTGAAAAG | 54629 |
rs148412482 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAM63B | GRCh38.p7 | 15:58836723 | TCCTGGGTTCAAGCG[A/G]TCCTCATGGCTCAGC | 54629 |
rs148444322 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAM63B | GRCh38.p7 | 15:58791585 | TCACAAGACTGCACT[C/T]TACCCTGGGCAACAG | 54629 |
rs148458856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58779288 | TTAACAGAAAATTCA[A/T]AGTTCGAATGGACGT | 54629 |
rs148480844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58824071 | GCTAGCCAAGAAGTA[A/G]TACTTGGATAAACTG | 54629 |
rs148534070 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | FAM63B | GRCh38.p7 | 15:58827732 | GCCGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 54629 |
rs148616074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58805936 | AAAAATTAGCTGGGC[A/G]TGGTGGCACGTACTG | 54629 |
rs148618257 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAM63B | GRCh38.p7 | 15:58780878 | CTCTCACCTGGACTA[C/T]CTTAGTAGCCTTCAA | 54629 |
rs148639454 | in-del | -/AAAAC | 0.469126 | 0.120349 | intron-variant | FAM63B | GRCh38.p7 | 15:58823665 | ACAGAATCTGTCTCA[-/AAAAC]AAAACAAAACAAAAC | 54629 |
rs148690315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58854352 | GTAATATAACAAATC[C/T]GTATGCCAATAGCTA | 54629 |
rs148709874 | snp | A/C | | | intron-variant | FAM63B | GRCh38.p7 | 15:58848137 | TGGGCAGTCTTGGAG[A/C]CACAGGTCTGTTTAT | 54629 |
rs148741065 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | FAM63B | GRCh38.p7 | 15:58860784 | TTTAATCCTTGAAGA[C/T]CTGTCTTGTATGTCT | 54629 |
rs148742923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58798735 | TGCTGGGATTACAGA[C/T]GTCAGCCACCACGCC | 54629 |
rs148797156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAM63B | GRCh38.p7 | 15:58802604 | AGATTTTTCCTTTTT[C/T]TCTCATTTTTTTCTC | 54629 |