SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2739 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400995 | ACTGTCTTCACACAG[A/G]GCATTCTTTCTCACC | 54467 |
rs10145 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401104 | ACCAAGGAAATACAA[A/T]TTGGATAATGATCAT | 54467 |
rs10946 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399125 | ACAAAGGAAATTCCC[C/T]GTAAGGTTAAAATAA | 54467 |
rs12740 | snp | A/G | 0.409382 | 0.192607 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399988 | TTATTAAGAAATTCA[A/G]TAAAACATCCTGCGC | 54467 |
rs38793 | snp | A/G | 0.437588 | 0.16526 | intron-variant, utr-variant-3-prime | ANKIB1 | GRCh38.p7 | 7:92397873 | AGGTAGCCTTTCTGA[A/G]CAGCCTCATTGCCTG | 54467 |
rs38794 | snp | A/C | 0.499577 | 0.0147501 | missense, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92398725 | GTGAAGGATGTGGAA[A/C]TGGTGCTGCCAGAAG | 54467 |
rs721015 | snp | C/T | 0.495252 | 0.0484902 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92295942 | TTCCAGCATCAGACT[C/T]CTATACCTGCATAAT | 54467 |
rs929171 | snp | A/G | 0.261608 | 0.24973 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92316287 | CAGACATAACTTTCT[A/G]TTTTGTCAAAGTAAG | 54467 |
rs975707 | snp | C/G | 0.474634 | 0.109726 | intron-variant, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245213 | GCGAGAAGTGAGTTA[C/G]AGGGGGAGAAGTGAG | 54467 |
rs1013522 | snp | A/G | 0.271432 | 0.24908 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258682 | CTGAAGTTTGGAATT[A/G]TAATTAATTTCATCA | 54467 |
rs1064819 | snp | A/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92244940 | TCATCAGTCATAGTG[A/G]CAACCAGAAATGCCC | 54467 |
rs1064820 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92244939 | CATCAGTCATAGTGA[C/G]AACCAGAAATGCCCT | 54467 |
rs1064821 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92244935 | AGTCATAGTGACAAC[C/T]AGAAATGCCCTCCAT | 54467 |
rs1137240 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92260519 | cctcccctctacaaa[A/G]ggtaaactaaattag | 54467 |
rs1142020 | snp | G/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245480 | GCAAGTTCGACTCCA[G/T]CGAGGGAAAACGGAG | 54467 |
rs1142021 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245471 | ACTCCAGCGAGGGAA[A/C]ACGGAGCCTCACCAG | 54467 |
rs1142022 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92244920 | CAGAAATGCCCTCCA[C/T]ATTTTCCAGTGATCC | 54467 |
rs1861635 | snp | C/G | 0.221553 | 0.248376 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92398223 | TCAGGCTCTGAGTTC[C/G]TTGGATGAAGACGAT | 54467 |
rs1978348 | snp | C/G | 0.26818 | 0.249338 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395577 | agatggagtcttgct[C/G]ttgttgcccaggctg | 54467 |
rs1978349 | snp | G/T | 0.345482 | 0.231048 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395873 | CACTTTCATATCCAG[G/T]TTCAAtggctcacac | 54467 |
rs2013491 | snp | A/G | 0.231189 | 0.249291 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92316702 | GCAGTTACCTTCAAC[A/G]ATGACTTCTCACACA | 54467 |
rs2040498 | snp | A/T | 0.338069 | 0.233974 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269803 | GGTCttttttttttt[A/T]aaaaaaattatactt | 54467 |
rs2097810 | snp | A/G | 0.456627 | 0.140731 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92347912 | TTGCATATAGTAATC[A/G]TTCAATAAATATTAC | 54467 |
rs2193239 | snp | C/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389367 | CAGTTAAGTGAAAAC[C/T]TAGACTGTTATAATG | 54467 |
rs2193240 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389656 | AACCTTTTGGTTGAC[C/T]TAAAGCTAGATTTGC | 54467 |
rs2287178 | snp | C/T | 0.0912534 | 0.193131 | downstream-variant-500B | ANKIB1 | GRCh38.p7 | 7:92402019 | AATATTTATCATTTA[C/T]GTGTTATGAATTAAA | 54467 |
rs2374563 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345443 | TTTTGTGACAACCAA[A/G]TTGCCTTGAAAATCT | 54467 |
rs2888876 | snp | A/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309942 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 54467 |
rs3020099 | snp | A/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92257235 | AAAAAGAAAAGAAAA[A/T]TTGTTACAATGAAGA | 54467 |
rs3041533 | in-del | -/TGT/TGTTT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261427 | TGTTTTGTTTTGTTT[-/TGT/TGTTT]GGCAACATACTACAC | 54467 |
rs3042461 | in-del | -/CA | 0.268515 | 0.249313 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311725 | AATAAGCGCCCCCCC[-/CA]CACACACACACACAG | 54467 |
rs3928926 | snp | A/C | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248603 | GGTAATTTTTCCCCC[A/C]TTGAGGATGCA | 54467 |
rs4141413 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307738 | GGTTTTTTTTTTTTT[G/T]attgtcttagtaatt | 54467 |
rs4266578 | snp | A/G | 0.270892 | 0.249126 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92281178 | tgttgaattatgaca[A/G]tgtgtatgaaatgta | 54467 |
rs4727269 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92257644 | CTAAAAATAGAAAAT[A/T]AGCTGAGCATGGTGG | 54467 |
rs4727270 | snp | A/G | 0.34526 | 0.23114 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92257875 | TAAACCAACTATTGA[A/G]ACTCAGGCCTTGTAA | 54467 |
rs4727271 | snp | C/G | 0.271432 | 0.24908 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270194 | cagccacccgagtag[C/G]tgggactgtaggcgc | 54467 |
rs4727273 | snp | A/G | 0.261884 | 0.249717 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92377615 | aatacagcaaagtgc[A/G]atgaaacaaggtatg | 54467 |
rs4729026 | snp | A/G | 0.264906 | 0.249555 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256378 | ATTCAGTTGGGGGTG[A/G]GATCTGGAAGCAAGG | 54467 |
rs4729027 | snp | A/T | 0.261608 | 0.24973 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331456 | TATTTTTAGTAGAGA[A/T]GGGGTTTCACCAGAT | 54467 |
rs4729028 | snp | A/G | 0.276267 | 0.248616 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331859 | TTGCCAAAAGTCTCT[A/G]CATTCAGCCAAATCA | 54467 |
rs4729029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354906 | TTCTTCAAAATCTCA[A/G]AAGTAATTTTCTAAA | 54467 |
rs4729035 | snp | C/T | 0.261608 | 0.24973 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92377073 | tttggctaactgaca[C/T]aagaagcctagcttt | 54467 |
rs4729036 | snp | A/G | 0.347032 | 0.230401 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389145 | TTAGGGGAAAAAAAC[A/G]AAAAGATACAGCAAT | 54467 |
rs4729037 | snp | A/G | 0.261608 | 0.24973 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389377 | AAAACCTAGACTGTT[A/G]TAATGATGTTCTTAA | 54467 |
rs5885804 | in-del | -/C | 0.259951 | 0.249802 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92316743 | CACACATTTTTTTAA[-/C]CCCCCCAATGAATGA | 54467 |
rs5885805 | in-del | -/ATAATA | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355882 | ATAATAATAATAATA[-/ATAATA]GTAATAGTAATAATA | 54467 |
rs6946462 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336151 | tttaatcagccatat[A/G]tattttaaataaact | 54467 |
rs6950017 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282050 | tctaaacttcgatac[A/G]tagtgtgtaattttt | 54467 |
rs6950926 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370340 | ggtgaaaccccatgt[C/T]tactaaaaatacaaa | 54467 |
rs6965321 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314565 | aatcccaaagggatt[C/T]ttatttaaagcttga | 54467 |
rs6965936 | snp | A/G | 0.494936 | 0.050064 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284904 | GGGTTTGTGAATTTA[A/G]GACATTGTTTTAATT | 54467 |
rs6972939 | snp | C/G | 0.497473 | 0.0354532 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333686 | ttcctatcattgtat[C/G]cccgctacctgacat | 54467 |
rs7384749 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383532 | cagcacatcaaaaag[C/T]ttatccaccaagatc | 54467 |
rs7780220 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356496 | ATTTAAATATCATGT[A/G]TACTCTCTGCAGAGT | 54467 |
rs7784492 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370214 | GGAGGATGAAGAAAA[A/G]TTGGGTAATGGGggc | 54467 |
rs7785589 | snp | A/G | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92330332 | TTAGGTATTGTTTCC[A/G]TAATACCTAATATAT | 54467 |
rs7787408 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92287905 | gccaggcatggcggc[A/G]tgcgcctgtagtccc | 54467 |
rs7791014 | snp | A/G | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359089 | TCCAGtttttttttc[A/G]tacttaagttctgtt | 54467 |
rs7796370 | snp | A/C | 0.317692 | 0.240661 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92272402 | tGTCAGCAACCTTGT[A/C]GAAGGAGAGAGTAGA | 54467 |
rs7796938 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354761 | TTAAAATCTAAGTGG[A/G]AATTGTCATATGCTT | 54467 |
rs7804001 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336602 | agatttggagagtct[A/G]tatccagaatctgtg | 54467 |
rs7807542 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379965 | accttggaagcataa[A/G]gggttgggggatttc | 54467 |
rs7807839 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380128 | aggtcccacacccac[A/G]gagccttgctcactg | 54467 |
rs7810095 | snp | A/T | 0.26518 | 0.249539 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338256 | ctctacaaaaaaatt[A/T]aaaaaaaaaaaaaat | 54467 |
rs9640603 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333345 | ctctagtcccatgct[A/G]tagctacactgacct | 54467 |
rs9690243 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367188 | GACAAAAGGCTGAAG[A/C]CACCTGAGATTTGTT | 54467 |
rs9691719 | snp | A/T | 0.344592 | 0.231414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383717 | aaaagctctcaatag[A/T]ctaggtattgatgga | 54467 |
rs9718935 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92287744 | ttgcaaatataaaag[A/G]aaaaaaaaaggccag | 54467 |
rs10215316 | snp | C/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92351676 | CAGATTTTACTGAGT[C/T]TAATATGTGAACTTT | 54467 |
rs10227853 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355876 | ataataataataata[A/G]taataataatagtaa | 54467 |
rs10227856 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355882 | ataataataataata[A/G]taatagtaatagtaa | 54467 |
rs10232840 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380418 | agctctgagaacgga[C/T]agaccacctcctcaa | 54467 |
rs10233202 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92300605 | tgtatatatttaagg[G/T]atacaatgtgatgtt | 54467 |
rs10233911 | snp | A/G | 0.497473 | 0.0354532 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375125 | atttaaaaatacttt[A/G]ttactaaaaaatgct | 54467 |
rs10236278 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380577 | tgttctgcaatattt[G/T]ctgttctgcagcctc | 54467 |
rs10236645 | snp | A/T | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293282 | gttattatacagcca[A/T]ggttgagaactacCC | 54467 |
rs10238257 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399345 | CTTTAAAAAAAAAAA[A/G]AAAGTTTTCTTCATT | 54467 |
rs10239410 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92276111 | AGTTGGTCTCATTAC[A/G]TCTCATTTAGATACA | 54467 |
rs10240009 | snp | A/G | 0.494733 | 0.0510469 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323789 | GAACTACTAATACAC[A/G]CTATATATAATATGG | 54467 |
rs10244041 | snp | G/T | 0.0444908 | 0.142359 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358012 | ctttgggaggccgag[G/T]cgggcatatcacaag | 54467 |
rs10245056 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288014 | gcactccagcctggg[C/G/T]gacagagcaagactc | 54467 |
rs10250316 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314063 | actactttggttggc[C/T]gaggcgggagcgtat | 54467 |
rs10263485 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389161 | aaaagatacagcaat[C/T]gcaaaggaagaagca | 54467 |
rs10266214 | snp | A/G | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293188 | ggagcttaaataccc[A/G]tgcctgggtgcttcc | 54467 |
rs10277068 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270671 | tgtccctgtatagtc[A/G]taccctctgccactc | 54467 |
rs10277246 | snp | C/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92301070 | attgtatatatgcca[C/T]atattctttatccat | 54467 |
rs10277500 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359109 | taagttctgttgtac[A/G]tgtgcagaacatgca | 54467 |
rs10488513 | snp | A/G | 0.275732 | 0.248672 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285661 | ATTAATTATTCTGTC[A/G]TAGGAAACAAGATCT | 54467 |
rs10488514 | snp | A/C | 0.39979 | 0.200158 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92322528 | AATGTAAAATAATTT[A/C]TTCATCCTGACTGTA | 54467 |
rs10623886 | in-del | -/TT | 0.347473 | 0.230215 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331920 | CATATAGAATCTAAC[-/TT]AACCTATAATTTCAC | 54467 |
rs10953066 | snp | C/T | 0.261332 | 0.249743 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278801 | ggaaaaaatcccatt[C/T]tggggaaagcttcct | 54467 |
rs10953067 | snp | A/G | 0.261332 | 0.249743 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278909 | ttgttgtaagttgca[A/G]tgaatcaagaaaccc | 54467 |
rs10953068 | snp | G/T | 0.347473 | 0.230215 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285437 | TTTATATTGGTGGAC[G/T]TTTTAGTCTTAAATG | 54467 |
rs10953069 | snp | C/T | 0.261056 | 0.249755 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293227 | CTCTGATTTTTGTTA[C/T]GAGATGTAGTTTGGT | 54467 |
rs10953070 | snp | A/G | 0.262435 | 0.249691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367738 | GCCTCTGTTGTGTCT[A/G]ATTAGAGCAAGAAGC | 54467 |
rs11267474 | in-del | -/CTCTTTTTTTTTCTTTTTAATT | 0.276267 | 0.248616 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355253 | AACCAATGACTTTTC[-/CTCTTTTTTTTTCTTTTTAATT]AAGTAAAATATGCTA | 54467 |
rs11311575 | in-del | -/T | 0.348794 | 0.229651 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92391496 | GACTTTTTTTGGTGA[-/T]TTTTTTTTTCCTCCA | 54467 |
rs11393456 | in-del | -/A | 0.405603 | 0.195673 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338418 | TGCCTCAAAAAAAAA[-/A]TAAAAATTAAAAAAA | 54467 |
rs11760878 | snp | A/G | 0.260504 | 0.249779 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92332908 | TACCTTAAACTCATC[A/G]TGTTTAAAACTAAGA | 54467 |
rs11763580 | snp | A/T | 0.262159 | 0.249704 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369334 | TTGCTGTGTGGAATT[A/T]AAAACCAATGCTTTT | 54467 |
rs11766996 | snp | A/C | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92320087 | CAAGACTCCAGTCct[A/C]ctgttcatcagtctc | 54467 |
rs11768934 | snp | A/G | 0.260504 | 0.249779 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261678 | GTTTTGATTTTGAGG[A/G]TTTTGTTCATTTTAG | 54467 |
rs11771536 | snp | A/C | 0.347914 | 0.230028 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387614 | GCACTCCAGCCTGGG[A/C]GACACAGCGAGACTC | 54467 |
rs11772754 | snp | C/T | 0.259951 | 0.249802 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92262222 | TATGGCAATAGAATG[C/T]GCTTAATGCTAAGAT | 54467 |
rs11971017 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378416 | ttgatgttgtacctc[A/G]tgttattggtatatc | 54467 |
rs11971507 | snp | A/T | 0.495213 | 0.048687 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92324205 | caccttaaagtggtt[A/T]attttatgttatgag | 54467 |
rs11972158 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278975 | gcagtggtccccaac[C/G/T]tttttggtactagag | 54467 |
rs11974646 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293868 | ATAGCTCAAGAATAG[A/G]TCCAGAAACAACGTT | 54467 |
rs11975525 | snp | A/G | 0.342582 | 0.232225 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358009 | GCACTTTGGGAGGCC[A/G]AGGCGGGCATATCAC | 54467 |
rs11976007 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303684 | ATTGAAAAAGTGTGA[C/T]TACAGAAGCCAAGGT | 54467 |
rs11977622 | snp | C/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92259847 | tcttatttttgtctt[C/T]tctctcacttctgct | 54467 |
rs11978229 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390783 | GCACTTTTATATAGT[C/T]TGCACTATGGCATCA | 54467 |
rs11978240 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92272991 | atcaaaacatagaaa[A/C]attatagtgaaaata | 54467 |
rs11979677 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283262 | AAAAGTGAATTTTAA[G/T]TCTGGAATTTATATT | 54467 |
rs12056285 | snp | C/G | 0.347032 | 0.230401 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92276495 | GGCCAGTCTTGCAAG[C/G]AGGCCTTTGTAAGGA | 54467 |
rs12530886 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269264 | ACCAGTTTTCTTAGG[G/T]GAGGGCTATAGTTGT | 54467 |
rs12532157 | snp | C/G | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350210 | CTTCAAAAAACTATG[C/G]TATATTTTAATGCCA | 54467 |
rs12533312 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269119 | TGAAAGTATTATGCA[A/C]TACCTATAGCATAGG | 54467 |
rs12536421 | snp | A/G | 0.409041 | 0.192888 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378906 | cagtcaacaacctTC[A/G]TGTGTATCAACAACA | 54467 |
rs12536804 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388239 | ACCCAGCACCTAGCC[G/T]CCTCCTCTTGATGCA | 54467 |
rs12539439 | snp | A/C | 0.381697 | 0.212499 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288051 | aaaaaaaaaaaaaaa[A/C]aaaaaactgccacca | 54467 |
rs12539878 | snp | A/C | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358641 | TGTTCTGACAGCAAA[A/C]CCAGTATTTACCAGC | 54467 |
rs12666899 | snp | A/G | 0.499368 | 0.0177603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361873 | GGAGTGCAATGGTGC[A/G]ATCTCGGCTCACTGC | 54467 |
rs12670516 | snp | C/T | 0.271432 | 0.24908 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255314 | AGTAATCATGTTCAG[C/T]GGCCACAGAAATCCA | 54467 |
rs12672992 | snp | C/T | 0.26078 | 0.249767 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329637 | GATCACAGCTGGACT[C/T]ATCATTTCTCCCATT | 54467 |
rs12704637 | snp | C/T | 0.316243 | 0.241064 | intron-variant, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245372 | CTCAAAGAGTTTCCA[C/T]CCAAAAAGTGGCTAT | 54467 |
rs12704638 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92253403 | TGGAACCACAACCCT[C/T]CACTGGGCCTATGAC | 54467 |
rs13220951 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338573 | GCTTTATAAATAAGG[G/T]TAGGTTTTGGCATTT | 54467 |
rs13223564 | snp | A/G | 0.390464 | 0.206809 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303352 | CTCAAAACATTTCAG[A/G]TTTTGGAGCATTTCA | 54467 |
rs13225256 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312419 | AAAATTATTTACAgg[G/T]cagcaaacttttctg | 54467 |
rs13230577 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338148 | aggtgtagtggctca[A/G]gtctgtaattttagc | 54467 |
rs13230852 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353527 | ATGGATACACTTAGG[G/T]GGATATGAAATTTTA | 54467 |
rs13231408 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92393204 | TAAATCAGATACTTT[C/T]TCTTTTCAGCTGCTG | 54467 |
rs13232519 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92381002 | acaaggaaggtaaaa[A/C]ccttgaaaaaagatt | 54467 |
rs13235429 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364212 | cagctactcaggagg[C/T]taaggcaggagaatc | 54467 |
rs13235542 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364309 | agagcaagactccat[C/T]taaaaaaaaaaaaaa | 54467 |
rs13236026 | snp | A/G | 0.40086 | 0.199352 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256559 | AACTGAGAACTAGGT[A/G]ACAACAATATGAGGC | 54467 |
rs13236437 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307831 | ttttttttttttttt[A/T]tgagacagagtcttg | 54467 |
rs13240665 | snp | A/C | 0.0146691 | 0.0843764 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312508 | acagacaatacagaa[A/C]caaaagagaatggca | 54467 |
rs13242676 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331147 | AATGTAGGATTAAAT[A/C]CAGTAAACGTTTCTT | 54467 |
rs13245461 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335239 | ctggatgttttattg[G/T]tttcacttcagtttt | 54467 |
rs13438254 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361011 | ctgggactacaggca[C/T]gagccaccactccct | 54467 |
rs17164460 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92257361 | TAGATAGCATACTTA[C/T]TAATTTAAGGTTCTT | 54467 |
rs17164465 | snp | C/G | 0.046775 | 0.145601 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92259299 | CATAATGTCCACGTG[C/G]CAGGTCGTAACCTAA | 54467 |
rs17164467 | snp | A/C | 0.2462 | 0.249971 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261030 | AATTGATAAAGTCCA[A/C]ACCTCTCTTGTTTGG | 54467 |
rs17164470 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263145 | TATGGGAATGAAATG[A/G]CAGGAGGTACATAAA | 54467 |
rs17164471 | snp | A/G | 0.191147 | 0.242974 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263394 | GATAAATGATACTGT[A/G]TTAAAAGAGGTAAAG | 54467 |
rs17164513 | snp | C/T | 0.273856 | 0.248859 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353384 | TCTTTTGACTATATA[C/T]GTGTCAGCCATCAGC | 54467 |
rs17164515 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365155 | CCTCTATGCTCTTGA[A/T]GTTTATATTTTAGAG | 54467 |
rs17164519 | snp | A/C | 0.25214 | 0.249991 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369181 | TTAGCCCTAAGTATA[A/C]TAAGTTCCTTCTGAA | 54467 |
rs17679665 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92349628 | TGTACTTCAAAAGTT[C/T]GTTTCTTGCTTTTCT | 54467 |
rs17685237 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358355 | AGTATTGCATTGGAA[A/C]CTGTACCAACCAGTT | 54467 |
rs17756839 | snp | C/T | 0.123105 | 0.215401 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261878 | ATCATGTCCTAACTT[C/T]TCTATTTGAAAGAGT | 54467 |
rs17757278 | snp | A/G | 0.021333 | 0.101051 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313025 | TAGTCATTAGGCCTC[A/G]TTATGTTTCCATTAG | 54467 |
rs17757926 | snp | C/T | 0.401747 | 0.198678 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358388 | AACACCCTGAAGTGG[C/T]CCTGCTGATTGGGCT | 54467 |
rs28365965 | snp | A/G | 0.254944 | 0.249951 | upstream-variant-2KB, utr-variant-5-prime | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245996 | AAAAGGAGCAGGAAC[A/G]GCAGCAGCCCGGCCG | 54467 |
rs28378808 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338255 | TCTCTACAAAAAAAT[A/T]AAAAAAAAAAAAAAA | 54467 |
rs28380045 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353798 | ACTTTATTTATGTAT[C/T]GTCTGTGCCTGCTTT | 54467 |
rs28427202 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261362 | TCAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAATT | 54467 |
rs28437555 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248554 | AATCTGAATGTCCTT[G/T]AAATGAAGTTGGAAA | 54467 |
rs28463248 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92297155 | AGGTAGTTTATTGTC[C/T]GTATTTTATAGGTGA | 54467 |
rs28529240 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92271300 | CCTGTTTCTGAATTC[C/T]TTTCTGTTGTATGAA | 54467 |
rs28561899 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92327196 | TTGCCATTATACTAT[A/G]ATATTTTATTTTTAG | 54467 |
rs28571910 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338253 | TGTCTCTACAAAAAA[A/T]TTAAAAAAAAAAAAA | 54467 |
rs28647645 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92304442 | GGATCTAGAGATATT[A/T]AATACTAGAGAGAGC | 54467 |
rs28656891 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355888 | ATAATAATAATAATA[A/G]TAATAGTAATAATAA | 54467 |
rs28663619 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355879 | ATAATAATAATAATA[A/G]TAATAATAGTAATAG | 54467 |
rs28697907 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255659 | GTTCTTATGAAATAT[A/G]TTTTTTTCTGTTCTT | 54467 |
rs28755784 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355885 | ATAATAATAATAATA[A/G]TAGTAATAGTAATAA | 54467 |
rs28814600 | snp | A/C | 0.254664 | 0.249956 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92384757 | GCATTAAAGACTTAA[A/C]TATTAGACCTAAAAC | 54467 |
rs28896529 | snp | G/T | 0.347694 | 0.230122 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92384414 | GGGAACCAAAAAAGA[G/T]CCCACATTGCCAAGA | 54467 |
rs33993294 | snp | A/C | 0.40157 | 0.198813 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369341 | GTGGAATTAAAAACC[A/C]ATGCTTTTACAGTCC | 54467 |
rs34008798 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248564 | TCCTTGAAATGAAGT[-/T]GGAAAAGATTCCTCA | 54467 |
rs34047879 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303469 | CTGGTCATACTTCCC[-/C]AATTTACAAAGTGTA | 54467 |
rs34058873 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285940 | TTTGATGATTTAGCC[-/C]TTAGTTATGCAATTC | 54467 |
rs34062479 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334057 | TGACTATATGTAAGA[-/C]AAATTGTTTGGATGT | 54467 |
rs34062641 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92271585 | GCCGGAAAACTTTTT[-/T]AAAAGAATATTTAAT | 54467 |
rs34091044 | in-del | -/A | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92298788 | AAAAAAAAAAAAAAA[-/A]GCAGTTTCCCCTAAA | 54467 |
rs34102223 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278534 | TACAAAATGTGTCCC[-/C]ATTTAACAATCTTAA | 54467 |
rs34104278 | in-del | -/TT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331921 | ATATAGAATCTAACA[-/TT]ACCTATAATTTCACC | 54467 |
rs34119329 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255066 | GTGACTTGCTCCTCC[-/C]TTGCCTTCTGCCATG | 54467 |
rs34121011 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273189 | GCCTTCAAATTCAAG[-/A]AAATAGAAAACTTAT | 54467 |
rs34145891 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374935 | AAGAATAAGGGAGAT[A/C]CAGCCATATCTCAGA | 54467 |
rs34176764 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92391232 | ACCTTCGCACACCCC[-/C]GCCACAAGATCATCA | 54467 |
rs34197906 | in-del | -/T | 0.492918 | 0.0590819 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92371176 | GGAGTAATATGTTGC[-/T]TTTTTTTTTTTAAAT | 54467 |
rs34219266 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92253265 | ATTTATCATTTCCCC[-/C]AGTTGTTTTATTTAT | 54467 |
rs34239167 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92343592 | TCCTAGCACTTTGGG[-/G]AGGCCAAGGTGGGTG | 54467 |
rs34265787 | in-del | -/T | 0.274124 | 0.248833 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92297667 | CTGGCATCTAAATGG[-/T]TTTTTTTTTTACAAG | 54467 |
rs34278792 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292538 | TTATTAATCTAATCC[-/C]AGAACTTTGGAAATG | 54467 |
rs34296377 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303175 | AAGTAACACAAATTG[-/G]AGCATCTCTTATTCA | 54467 |
rs34303457 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390262 | GTTTTTAAATAAAGG[-/G]AAAAGTTACCAGTAA | 54467 |
rs34306068 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248733 | GTCTGTGGGAGTTTT[-/T]ATACATTGATCTAAA | 54467 |
rs34307308 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401022 | AGTGTACACAATGGG[-/T]TTCCGGTTTCCTTGC | 54467 |
rs34318038 | in-del | -/A | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370540 | AAAAAAAAAAAAAAA[-/A]GTTGGTTAATGGGGA | 54467 |
rs34323757 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289551 | AGCATAGTTTCAAAA[-/A]TTAGTCCGTGGTTCT | 54467 |
rs34362735 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369130 | ATTATAGCAATACCC[-/C]TTTGTAAGTGGAATT | 54467 |
rs34399457 | in-del | -/C | 0.44546 | 0.155869 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280451 | AACGTTTGGAGGGCA[-/C]CCCCCCCCCCTTTTT | 54467 |
rs34404682 | in-del | -/GTGT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290404 | TGTGTGTGTGTGTGT[-/GTGT]ATTGGGACCTGCTGC | 54467 |
rs34411750 | in-del | -/C | | | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247721 | CATTTGCTACTTTTC[-/C]AGAGCACCATAGGAA | 54467 |
rs34421121 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345489 | TTTAAAATTTCTTTT[-/T]AGTGAATGCAGAGTT | 54467 |
rs34422207 | in-del | -/T | 0.399968 | 0.200024 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358538 | GCTTTTTTTTTTTTT[-/T]CAGACTTTATTTGAA | 54467 |
rs34433516 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268079 | CATTCTTTCTGTGTA[-/A]CTTTTGTTTTGTTTA | 54467 |
rs34445590 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92318635 | ACTTGAACCTACAGT[-/G]CCTTAATAACAACAT | 54467 |
rs34459328 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329405 | ATAACCCCAGAGAAT[-/A]CTAAGTCATTAGGTC | 54467 |
rs34482010 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354303 | CCCCAAAATATCAGG[-/G]CTGGTTATACTCAAG | 54467 |
rs34483972 | in-del | -/T | 0.471004 | 0.116864 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92286496 | AGGATATTATCCGTA[-/T]TTTTTTTTTTTTTTT | 54467 |
rs34497530 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248934 | TTCTCTTGCCAAGGC[-/C]TGGAGTGCAGTGGTG | 54467 |
rs34502019 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369565 | TTACTTCCCCAGGGG[-/G]CTTATATCTAGGGGT | 54467 |
rs34545193 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268014 | GGTAGAAGAGAAAAA[-/A]CGAGTTCAAGTACAG | 54467 |
rs34557370 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266315 | GAAAAGGGAAAGTTT[-/T]AATATAAAGAATTAT | 54467 |
rs34632900 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92393828 | CATTGTGAGACTTTC[-/C]AAATTCTGCATGTGT | 54467 |
rs34651708 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361532 | CAGGAATACACCTTT[-/G]GAATAACAAGAATTT | 54467 |
rs34700026 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386204 | GATTAGAATGCACTT[-/T]AAAAATGAAACACTT | 54467 |
rs34749774 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367622 | CTCAGGATGAGAAAA[-/A]TCTAATTAATGAGAA | 54467 |
rs34766543 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323720 | CTAATGAATGGGTAA[-/C]ACAAGATGTGAGATA | 54467 |
rs34891046 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92252404 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 54467 |
rs34917329 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268702 | CTTGTCTCTAACTCC[-/C]TGGACCCAAACGATC | 54467 |
rs34919563 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369134 | TAGCAATACCCTTTG[-/G]TAAGTGGAATTGCCT | 54467 |
rs34930995 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336840 | TCTGCCTGCTTTTGG[-/G]TTGCTCTCTAGTGTC | 54467 |
rs34931227 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92254716 | TGTTCTTTGATATCC[-/C]TTATTATGGATATAA | 54467 |
rs34994800 | in-del | -/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270752 | TTTTTTTTTTTTTTT[-/T]GAGAATGTCATATCA | 54467 |
rs35001937 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284962 | TTAGGATAAGCTTTT[-/T]AGGTATCTAGCGTAG | 54467 |
rs35009495 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92299822 | ATTTTGTTTTTTTTT[-/T]CTGAGACAGGGTCTT | 54467 |
rs35010422 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92396988 | AACTTTTAAATGTTA[-/G]AATTATTAAGTGAAA | 54467 |
rs35028119 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395560 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 54467 |
rs35055406 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269183 | TGTCTCACCCTGTTT[-/A]CTTAGATTGAATCAG | 54467 |
rs35086466 | in-del | -/TTT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358773 | ATTGCATTTGTTTGT[-/TTT]AGTTACTGCAGATAT | 54467 |
rs35099467 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280410 | AAGGGTGATGGGGTT[-/T]GGTGTAGCAGCAGCT | 54467 |
rs35133808 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248740 | GGAGTTTTTATACAT[-/T]GATCTAAAAATGTTT | 54467 |
rs35149498 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308566 | ATTTGCGTTAAAGTG[C/T]TCCTGAATACATACT | 54467 |
rs35203954 | in-del | -/CAGTACTTGCCTCAT | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292016 | GCCTGTTTGGTACTC[-/CAGTACTTGCCTCAT]GAAGCTCTATACATA | 54467 |
rs35210542 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92391765 | TGAAGGAAAGAGAAA[-/A]TTTGATATTTGTAGT | 54467 |
rs35237464 | snp | A/G | 0.0422008 | 0.138995 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342479 | GTTCAAGATCACTTA[A/G]TATAGAATTTATACC | 54467 |
rs35297077 | snp | A/T | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92250445 | TATCAAAAATAATTT[A/T]CAGTCATTGTTTAAA | 54467 |
rs35318216 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284316 | GTATTACCTATGGGG[-/G]AATGTAAAATTTCCT | 54467 |
rs35321105 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288493 | AGTCAATTGGCTTTT[-/T]ACAAAGATTCAAAGG | 54467 |
rs35331536 | in-del | -/TT | 0.231482 | 0.249313 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350142 | AGTAGGAAATAAAAC[-/TT]ATTTTAATATTCATC | 54467 |
rs35351716 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92301036 | GATTTCCTTCTTTTT[-/T]AAGACTGAATAATAT | 54467 |
rs35399470 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268599 | CTCCCACCTCAGGCT[-/T]CCCGTAGCTGGGATT | 54467 |
rs35441868 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291113 | GCCTGGCCAAAATGG[-/G]CGAAACCCCGTCTCT | 54467 |
rs35462188 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264975 | ATCTCTGAGAACATG[-/G]ATATTTTTTATTTTA | 54467 |
rs35525211 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340106 | CACTGAATTTTTTTT[-/T]AAATGATGGCTTTGT | 54467 |
rs35579725 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284362 | ATTGCCGTTACATTT[-/T]CTAAAGGCCTTCTTT | 54467 |
rs35584170 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293805 | GTGTAGGCCTTTTTT[-/T]CATACCTGCCTTTGC | 54467 |
rs35592110 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350611 | GCATATAACCCCAGG[-/G]CTTTGGGAGGCCAAG | 54467 |
rs35606982 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270857 | GTTGTAGCATTTTCC[-/C]TTGTTGGATGTGTGA | 54467 |
rs35631070 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268655 | AATTTTTGTATTTTT[-/T]AGTAGAGACCAGCTT | 54467 |
rs35685363 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92368840 | TAGTTGGTTATTCCC[-/C]TGAACATGATTTACT | 54467 |
rs35708590 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344384 | TAATTTTTGTATTTT[-/T]GGTAGAGACAGGGTT | 54467 |
rs35734467 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358551 | GGCTTTTTTTTTTTT[-/T]CAGACTTTATTTGAA | 54467 |
rs35766675 | in-del | -/A | 0.494692 | 0.0512434 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288036 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 54467 |
rs35798241 | in-del | -/T | 0.270892 | 0.249126 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261028 | AAATTGATAAAGTCC[-/T]AAACCTCTCTTGTTT | 54467 |
rs35818557 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92301954 | TTTTCTTTTTTTTTT[-/T]GAGACGGAGTCTCAT | 54467 |
rs35941213 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291122 | AAATGGCGAAACCCC[-/C]GTCTCTACTAAAAAT | 54467 |
rs36036440 | in-del | -/AGTT | 0.395453 | 0.203331 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303038 | TCTGGGAGAAAAGAC[-/AGTT]AGTTCAGAGAGAGTT | 54467 |
rs36061214 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92276614 | TAGAGGTCCAGAATG[-/T]GGCCAGTTAAAACAA | 54467 |
rs36068183 | in-del | -/T | | | intron-variant, utr-variant-5-prime | ANKIB1 | GRCh38.p7 | 7:92347984 | TACCTATGATATCAT[-/T]CTGTGAATTTTACCT | 54467 |
rs36091746 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92252525 | CCGAGTAGCTGAGAT[-/T]ACAGGCACCCACCAC | 54467 |
rs36102367 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291076 | GGTGGGCAGATCACC[-/C]TGAAGTCAGGAGTTC | 54467 |
rs36201067 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383599 | CATACACAAATCAAT[-/T]AAACGTAATCCATCA | 54467 |
rs55647943 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323427 | AACTTTGTGTATTTT[C/T]CCATATCCTAAGTTT | 54467 |
rs55660961 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375951 | TTTCCTTGTACATCT[C/T]CATCAGAGCTCTTGG | 54467 |
rs55734309 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311706 | TGTAATAATTATGTT[C/T]TGTAATAAGCGCCCC | 54467 |
rs55768559 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334018 | CTAAACATTTTTCAA[C/T]AGTTATTATAATGAC | 54467 |
rs55894122 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334713 | TTATAACAATAGTAT[A/G]CTTAATCTACATATG | 54467 |
rs55936298 | in-del | -/GTGT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372009 | TGTGTGTGTGTGTGT[-/GTGT]ATCAAATGATTAACA | 54467 |
rs56001829 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334344 | ATTCAAGAATTCCTG[A/G]TTCCAAGGGATAATC | 54467 |
rs56006273 | snp | A/G | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255491 | CCTCGTGGTCTTCAG[A/G]TGGCATTCCAGACTG | 54467 |
rs56236313 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289885 | TGGGTAGCACTATCT[C/T]GGCTCACTGCAACTT | 54467 |
rs56238133 | in-del | -/T/TTT | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358605 | ATTCTTTTTTTTTTT[-/T/TTT]CCCAGAACATTTTCA | 54467 |
rs56362370 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92332956 | AACCTGGTTCTCTGG[G/T]GTTCCCTAACTCCAT | 54467 |
rs56718705 | in-del | -/T | 0.128976 | 0.218754 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296236 | CCTAATTTTTTTTTT[-/T]AATAGAAACGGTGTC | 54467 |
rs57088700 | snp | C/T | 0.346147 | 0.230772 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284015 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 54467 |
rs57433727 | snp | C/T | 0.0926964 | 0.194308 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400943 | CCAATATAGAGTCTT[C/T]GCATCACACTGAGGC | 54467 |
rs57505071 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92330046 | TATGACATAATCTTT[A/T]CCTAGACTGTCAGTC | 54467 |
rs57536267 | in-del | -/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309940 | AAAAAAAAAAAAAAA[-/T]AAATATATATATATA | 54467 |
rs58075588 | snp | A/G | 0.0704125 | 0.17392 | upstream-variant-2KB, utr-variant-5-prime | KRIT1, ANKIB1 | GRCh38.p7 | 7:92246057 | GGCAGGCGACTAGGA[A/G]ACTAGGGTGGTGGCG | 54467 |
rs58197600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92281198 | TATGAAATGTAATCT[C/G]CCAAAGAAGTTCCTT | 54467 |
rs58955889 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365422 | GGCAATATGAAGTAG[C/T]GTGGCATATTCAAAG | 54467 |
rs59131137 | in-del | -/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365816 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCGCTC | 54467 |
rs59213993 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92381513 | CAGGTTACCCACAAA[A/G]GAAAGCCCATCAGAC | 54467 |
rs59242586 | snp | A/G | 0.408017 | 0.193729 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288831 | TACTACACATCCATT[A/G]TAATGGCTACCAAAA | 54467 |
rs59410969 | in-del | -/AAAAAAAAAA | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370531 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GTTGGTTAATGGGGA | 54467 |
rs59479934 | in-del | -/ATT/T/TT | 0.237318 | 0.25019 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307661 | CTGTGTAGAGGTAAA[-/ATT/T/TT]TTTTTTTTTTTTTTA | 54467 |
rs59848454 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92371946 | GTGAGAGTCTTGAGA[A/G]AGGGGTGTGTGTGTG | 54467 |
rs59895741 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266404 | TATATGTAGCAGATA[C/T]AGGGAGCAACCATTA | 54467 |
rs59964758 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386236 | CCAAAGATATTATTT[A/G]GAAAGAATGGTTCCT | 54467 |
rs60029536 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280181 | GGATGATCCCTCTAG[-/C]ATTTATGAAATTACA | 54467 |
rs60063984 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92349977 | CCCAGGAGTTTGAGA[C/G]CAACCTAGGCAAAGA | 54467 |
rs60522228 | snp | A/G | 0.344147 | 0.231595 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266986 | GAGTTGAGAGGCAGT[A/G]AGTTGACAGTTGGCA | 54467 |
rs60553937 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401128 | CCTTGGTACATATTT[-/T]AAAAACAACACAGTC | 54467 |
rs60664984 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365830 | TTGAGACAGTCTCGC[C/T]CTGTCGCCCGGGCTG | 54467 |
rs60766571 | in-del | -/AG | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365823 | TTTTTTTTGAGACAG[-/AG]TCTCGCTCTGTCGCC | 54467 |
rs61386358 | snp | G/T | 0.0930568 | 0.194599 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306448 | AATTAGATCTTAGTC[G/T]TCTAGATCTAACCAC | 54467 |
rs61644094 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338757 | TCTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC | 54467 |
rs61678990 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92371944 | CAGTGAGAGTCTTGA[A/G]AGAGGGGTGTGTGTG | 54467 |
rs61740421 | snp | C/T | 0.0268142 | 0.112642 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92397766 | CAGGCCTGGCACATC[C/T]GTGGTAAGTTCTGCA | 54467 |
rs62467796 | snp | C/T | 0.120326 | 0.21374 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92251930 | GTTGTTATGTCTGTT[C/T]GTAGTTCTTCAGCCT | 54467 |
rs62467797 | snp | A/G | 0.392696 | 0.205275 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92260408 | ACTTTGGGCTTGGCC[A/G]GTGGCTCACCTGTAA | 54467 |
rs62467798 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92267719 | GATTATTTTTTCCAT[A/G]TGGATATGCAGTTGA | 54467 |
rs62467799 | snp | A/G | 0.122411 | 0.214991 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277428 | TGGCTTTATTCAGAT[A/G]TAACCCCATCATAAG | 54467 |
rs62467800 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279246 | CCTAACAGGCCATGG[A/C]CAGGTACCAGGCTAC | 54467 |
rs62467832 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290983 | TAGAATTTATTGTAC[A/G]TTTTAAAATAACTAG | 54467 |
rs62467833 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92302514 | CCTCTTTTGTGGGAA[A/C]CTAAATCCATACTCA | 54467 |
rs62467834 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303881 | GTAGAAGAAATAGAG[A/G]TAACAGCTATAAACT | 54467 |
rs62467835 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303895 | GGTAACAGCTATAAA[A/C]TGGCTGCTTAAGAAT | 54467 |
rs62467836 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92328988 | TTTTTTTTTTTTTGG[G/T]ACAGAGTCTTGCTCT | 54467 |
rs62467837 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329125 | GGTGCACACCACCAC[A/G]CCCGGCTAATTTTTG | 54467 |
rs62467838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329128 | GCACACCACCACACC[C/T]GGCTAATTTTTGTAT | 54467 |
rs62467839 | snp | A/G | 0.408871 | 0.193029 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338057 | GGGTGTAGTTTAGGC[A/G]AGAAATAGGAAATAG | 54467 |
rs62467840 | snp | C/G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344184 | TTTTGTTGTTGTTTT[C/G/T]TGTTTTTGGTTTTTT | 54467 |
rs62467841 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345813 | CTTTTTTTTTTTTAA[A/T]TAGAGTATCAGTTAG | 54467 |
rs62467842 | snp | A/G | 0.118584 | 0.212673 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356557 | GGGTTCAATTTATCA[A/G]ATTTCAACACAGTAC | 54467 |
rs62467843 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359731 | TCCTCTCCAGCATCT[G/T]TTGTTTCCTGACTTT | 54467 |
rs62467844 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361830 | GTTTTTTTTTTTTAA[A/T]TGGAGTTTCACTCTT | 54467 |
rs62467845 | snp | C/T | 0.116138 | 0.211142 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366996 | AGTGAGAACAGATTA[C/T]GGGCGGGACTGTGAA | 54467 |
rs62467846 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372468 | AATCCTCCATGGATA[C/T]CAGGGAACACCTATA | 54467 |
rs62467847 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383697 | ATTCAACAGCCCTTT[A/G]TGCTAAAAGCTCTCA | 54467 |
rs62467848 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92385965 | TAACTGACTCAAAAT[A/C/T]CTAAGCATAAGAAAG | 54467 |
rs62467849 | snp | C/T | 0.118933 | 0.212888 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386708 | ACTGGAATTATTTTG[C/T]ATTTCTTTTTCTATT | 54467 |
rs66506083 | in-del | -/T | 0.0955749 | 0.196603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358594 | ATTCTTTTTTTTTTT[-/T]CCCAGAACATTTTCA | 54467 |
rs66624934 | in-del | -/ACAC | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372003 | TGTTAATCATTTGAT[-/ACAC]ACACACACACACACA | 54467 |
rs67933063 | in-del | -/AAAAAAAAAAAA | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344210 | GTGAAACTCCGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 54467 |
rs68109065 | in-del | -/AG/GG | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365822 | TTTTTTTTTGAGACA[-/AG/GG]GTCTCGCTCTGTCGC | 54467 |
rs71107855 | in-del | -/A | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307832 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 54467 |
rs71107856 | in-del | -/TATTATTAT | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355879 | TATTATTACTATTAC[-/TATTATTAT]TATTATTATTATTAT | 54467 |
rs71292983 | multinucleotide-polymorphism | GCTAACACAGTGAAACCCCATCG/TCCAACATGGTGAGACCTTGTCT | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339251 | ATCAAGACCATCCTG[lengthTooLong]CTACTAAAAATACAA | 54467 |
rs71292984 | in-del | -/AC | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339216 | GTCTCTACTAAAAAT[-/AC]AAAAAAATTAGCCTG | 54467 |
rs71560810 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288050 | CAAAAAAAAAAAAAA[A/C]AAAAAACTGCCACCA | 54467 |
rs71560811 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288821 | TGTACAATACTACTA[C/T]ACATCCATTATAATG | 54467 |
rs71560812 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331160 | ATACAGTAAACGTTT[C/T]TTAATCATGTAATAG | 54467 |
rs71560813 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339256 | ACCATGTTGGACAGG[A/C]TGGTCTTGATCTCCT | 54467 |
rs71560814 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339266 | ACAGGATGGTCTTGA[A/T]CTCCTGACCTGGTGA | 54467 |
rs71560815 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357692 | GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 54467 |
rs71560818 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386919 | TTAACATTAATATCA[A/C]CAATGCAGTATTACA | 54467 |
rs71670038 | in-del | -/AG | 0.191461 | 0.24305 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92363814 | TTTGTCCACTGACTC[-/AG]GGTTATTCTGACCCA | 54467 |
rs71728712 | in-del | -/TTC | 0.0452528 | 0.143452 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247021 | GAGCGCTCCCCTGTA[-/TTC]TTATTCTTCTCCGTA | 54467 |
rs71840452 | in-del | -/CCT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362546 | CCATTTAATCCTCCT[-/CCT]ATAGCCCTTTTCTTT | 54467 |
rs72329256 | in-del | -/TCC | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362539 | GGGGGTCCCATTTAA[-/TCC]TCCTCCTATAGCCCT | 54467 |
rs73230404 | snp | C/T | | | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247870 | ATTAAGAAAGATGGA[C/T]GTGTTTAATGACTTT | 54467 |
rs73230419 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283556 | AAGGTCTGTCTCCTG[C/T]TCCTGGTTTTGTACT | 54467 |
rs73230434 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340050 | TTGGCCTTAAAGAAC[A/G]TTAATTTGTGTCTCA | 54467 |
rs73230436 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350716 | TTAAAAATTAGCCCA[A/G]CATAGCAGCATATAG | 54467 |
rs73230440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356823 | GTGCATGTAAAATGG[A/G]GATAAATAGTACCAG | 54467 |
rs73230441 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356827 | ATGTAAAATGGGGAT[A/C]AATAGTACCAGTTAC | 54467 |
rs73230450 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388388 | AGGAGCAAGATACAC[A/G/T]TGCTACCCAATTGTC | 54467 |
rs73407592 | snp | A/G | 0.0930568 | 0.194599 | upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92246171 | CTGGAACATGAGCCG[A/G]GCTTGACCGCGAGGC | 54467 |
rs73407593 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248450 | CTCAAACTTGTGAAA[A/G]TGAAATATGTGTATT | 54467 |
rs73407596 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92265463 | AGGGGCCAGTGTAGC[C/T]GGAGCATACTAAGCA | 54467 |
rs73407599 | snp | C/T | 0.110167 | 0.207236 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275545 | GCGAAATGTGAGGGA[C/T]GGTCCTACACAGTGA | 54467 |
rs73407600 | snp | A/G/T | 0.110167 | 0.207236 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275653 | GACATAGAACTGGGG[A/G/T]TGATGCACCATTCTG | 54467 |
rs73414030 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277652 | TTATGGATGTTCTGT[G/T]TGAAAGTGCAGGGAG | 54467 |
rs73414035 | snp | A/G | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294791 | GTTGGTTCCCTTATC[A/G]ATGATTCCCAGATTT | 54467 |
rs73414037 | snp | A/C | 0.346811 | 0.230494 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296900 | GTATTTCTTTTATCT[A/C]ATTTTTTTGCTTCTA | 54467 |
rs73414038 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305639 | GGCTTCTAAGTAGTG[C/T]TGGTTTGCTTAAGTG | 54467 |
rs73414039 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315419 | ATCTACATAGAGTTG[A/G]CAGCTAAAAGCAAGA | 54467 |
rs73414041 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323084 | TCATGATTATTACTT[C/T]GTAGTCGTCATTATT | 54467 |
rs73414044 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92326954 | AGTAGCTGAGACTAT[A/G]GGCATTCACCAAGTT | 54467 |
rs73414047 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333868 | TTTTATTAAAAAGTA[A/G]CATAATGGAAATTTT | 54467 |
rs73414049 | snp | A/C | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336030 | GTACCACTTCCCATA[A/C]AATGTAAGAATCTTG | 54467 |
rs73414052 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339884 | TAATTTCTACTTTGC[C/G]TTTATCACCTTCTTC | 54467 |
rs73414055 | snp | A/T | 0.345037 | 0.231231 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92351845 | TGTGCCTCAGCCTTA[A/T]GAGTAGCTGGGATTA | 54467 |
rs73414060 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366428 | CCCCAAATTTGATCT[A/G]TTACCCTGAAAGAAC | 54467 |
rs73414066 | snp | A/G | 0.347253 | 0.230308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387270 | AATACAGTCACATAG[A/G]GGGTAGGGCTTCAAA | 54467 |
rs73414072 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92393123 | TTTGTAATGTATAAC[C/G]CATTTGTTACCTGCA | 54467 |
rs73711593 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308789 | TTCATATCCATCCTT[A/G]CATATCTCATAGAAG | 54467 |
rs73711594 | snp | C/T | 0.093417 | 0.194889 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315240 | GGTGAAATGGAGAAA[C/T]TGGTTGAAAGGAAGA | 54467 |
rs73711595 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315246 | ATGGAGAAATTGGTT[C/G]AAAGGAAGAGAGAAT | 54467 |
rs73713703 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336077 | TTGCCCCATCCCTTA[A/T]GCTATCATTATTATA | 54467 |
rs73713704 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364865 | ATTTTTAGTTTGGGT[C/T]GGAGGGTAAATTATG | 54467 |
rs73713706 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367430 | TATACAAAAATGATA[C/T]TTCAAAAAGGAAAAG | 54467 |
rs73713707 | snp | A/G/T | 0.0926964 | 0.194308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92371190 | CTTTTTTTTTTTTAA[A/G/T]TTTTTTTGTGTATAT | 54467 |
rs74298195 | snp | C/T | 0.262159 | 0.249704 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92351584 | TTTGTCTTCATTCTT[C/T]TTCAGAAGTTGTAAG | 54467 |
rs74313100 | in-del | -/CTC | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387084 | CTTGATGAGGGTTCT[-/CTC]CTTGGTTTGCAGACA | 54467 |
rs74330577 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357235 | TAGATTAGGCAACTA[A/T]TTTTTTTTTCTTTAT | 54467 |
rs74358651 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400395 | TGTTTTACTTAAATA[C/T]TATCAAAACTAGCAT | 54467 |
rs74395907 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278087 | GAAACTCTGTGTCAA[A/C]AAAAAAAAAAAAAGT | 54467 |
rs74668307 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311515 | CCTGTTTCTTGACTA[C/T]ATCTGTGGAAGTATA | 54467 |
rs74719510 | in-del | -/TT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345809 | TAACCTTTTTTTTTT[-/TT]AAATAGAGTATCAGT | 54467 |
rs74752799 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92351359 | TTTATCAGAACTTTT[G/T]ATTAATTTGCCCGTT | 54467 |
rs74797352 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342341 | CCTAGCAAAGTAATT[C/G]AATGTATTAGTTTGT | 54467 |
rs74897167 | snp | C/T | 0.260504 | 0.249779 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309304 | TGTCCAGGCTGGTCT[C/T]AAACTCTTGGGTTTA | 54467 |
rs74904464 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359087 | TATCCAGTTTTTTTT[C/T]CATACTTAAGTTCTG | 54467 |
rs74930658 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279823 | TTCTTAAGCCTTTTT[A/T]ATCCTGGCAACCTTA | 54467 |
rs74952383 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312095 | TTTTAAATTGCATCA[A/G]ACTCATACTACCCAT | 54467 |
rs75116927 | snp | A/G | 0.0150606 | 0.0854603 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399842 | GACACTTTATTGGAA[A/G]TGCAATCATAGTTAT | 54467 |
rs75124428 | snp | A/G | 0.113334 | 0.209338 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319869 | GAGTCCAAGAGTTCA[A/G]GGCTGCCATGAGCTA | 54467 |
rs75142415 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282044 | TAGATTTCTAAACTT[C/T]GATACATAGTGTGTA | 54467 |
rs75174020 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354132 | CCATTCTCTTTGTAT[A/G]CTGCAAGTAATAATA | 54467 |
rs75175622 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275381 | AAAAGTATTGTTCCC[A/G]ATTGTTTTAATGATT | 54467 |
rs75181108 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92298813 | CCTAAAAAAATCCTC[G/T]ATTAAAGCAGTAAAA | 54467 |
rs75185170 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290218 | TCTGTTTGATTTCAA[C/G]CTGGAGTGGGATGGG | 54467 |
rs75207460 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92310794 | AAACGTGGATGTTCA[A/G]TACAGACACAACCAT | 54467 |
rs75208333 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266547 | GGGTACTGCACTTAA[A/G]GAACTCACCTGTAGA | 54467 |
rs75291964 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92363794 | TTTAGATCTACGAGG[A/G]TCATTTTGTCCACTG | 54467 |
rs75329884 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92337171 | TTCGTCCTTTACTGT[A/G]TACTAAGCAGTAAAC | 54467 |
rs75330762 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92297947 | ACTTAGCTTCATTCC[G/T]GTTGTTTCTGGATTC | 54467 |
rs75401615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372235 | AAAAATTGCATCTGT[A/T]TCGAACATGTACAGA | 54467 |
rs75476916 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365733 | GAAGGCTTAAGATGG[A/G]TAATTCAGGTGGGAG | 54467 |
rs75507371 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390948 | AAATGAGCGCTTTTT[A/T]AAAAATTCACATGAT | 54467 |
rs75619787 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344209 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]GAGACGGAGTTTCAC | 54467 |
rs75624974 | snp | A/G | 0.274929 | 0.248754 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92349197 | CAGAGCTGGCCAGAG[A/G]ATTTGAGGATTAGCC | 54467 |
rs75637675 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321478 | ATTAGACTGTCAATT[A/C]CATGAAGGCTAGAGC | 54467 |
rs75670577 | snp | G/T | 0.0327778 | 0.123752 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367783 | TTTTTATGAAATGAT[G/T]GTTAATTTATAAATT | 54467 |
rs75719792 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399106 | TGAATGGTAGCTTCA[G/T]TTTTTATTTTAACCT | 54467 |
rs75726584 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92317364 | TCTAACAAATTCCCA[A/G]GAGATACTACTGGTC | 54467 |
rs75839896 | snp | C/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390144 | TAATTACATTTAAAT[C/G]GCAGCAGTTATTATG | 54467 |
rs75924911 | snp | G/T | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275601 | AGAAGAAGACAGGAG[G/T]TGTATTAACCTGGAA | 54467 |
rs75930435 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340520 | CCATTGGAATACCAA[A/G]AAAAAAAAAGGATGA | 54467 |
rs76043196 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294847 | TGTTTCTTTTGTGAT[G/T]ATTGTTTTACAATCT | 54467 |
rs76089140 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294666 | GCCTGTGAAACCTTA[A/G]CAGTCTCTGTGTGGG | 54467 |
rs76131937 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92391979 | AGTAAATATTTACTT[G/T]TAAAATACAAATAGA | 54467 |
rs76209380 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314895 | GTGAACTGACAAAGC[A/G]TCTGGGTTTGTGTGG | 54467 |
rs76219885 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255778 | GGGCTGTCATGTTTT[A/G]AAGTTATTTATACGC | 54467 |
rs76242221 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395998 | TAAAAATAAAAAAAT[A/G]AAAAATAAAAAACCT | 54467 |
rs76270287 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339483 | CTTCAGCTGTAATCA[G/T]TTACAATTTCCTGGA | 54467 |
rs76301906 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354258 | TCTAGAATAACATTT[A/G]GAGAAATACATCAGC | 54467 |
rs76301986 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306428 | GAGATAAACACTCAC[C/T]GTGGAATTAGATCTT | 54467 |
rs76318974 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319802 | TTGCCAGGAATGGTG[A/G]CCCACACTCATTGTC | 54467 |
rs76338345 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92267541 | TACTCCTAAAAAATC[C/T]CCATAGAGATTTTTA | 54467 |
rs76449800 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | ANKIB1 | GRCh38.p7 | 7:92398171 | TTAAATCAGTTTTTT[C/T]CAGTCAAATTTTAAA | 54467 |
rs76569377 | snp | A/G | 0.347253 | 0.230308 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380236 | ACGGCTGGGAAGCTC[A/G]AACTGGGTGGAGCCC | 54467 |
rs76574735 | snp | G/T | 0.261608 | 0.24973 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92384895 | AAACATGGGATCTGA[G/T]TAAACTAAAGAGTTT | 54467 |
rs76631110 | snp | A/C | 0.273318 | 0.24891 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92341507 | GCAAAAAAAAAAAAA[A/C]TGTAAACAAAGTAGG | 54467 |
rs76667776 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344189 | TTGTTGTTTTGTGTT[G/T]TTGGTTTTTTTTTTT | 54467 |
rs76718820 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92251910 | AGGAATACATGTTAC[A/G]GTTGGTTGTTATGTC | 54467 |
rs76729539 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389066 | CCTTAACAACATTCA[A/G]TATTTGTAGATGTGA | 54467 |
rs76890500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344697 | TGTTTCTTGTACTTC[A/G]TTTTCCAAACGCACA | 54467 |
rs76892626 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273056 | GTACAGTATTTGCCA[C/T]ATAACATTTTGGTCA | 54467 |
rs76922447 | snp | A/C | 0.0348642 | 0.127344 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92398592 | TGACAATCTTCTCGG[A/C]AACATCATGGCTTGG | 54467 |
rs76959827 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92297728 | TTTTACTAAAGCATA[A/G]CCTTTCAGTGTTCTT | 54467 |
rs76988735 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350018 | CTTAAAAAAAAAAAA[A/G]AGAAAGAAAAGGAAA | 54467 |
rs77101858 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290423 | GGGACCTGCTGCCTG[A/C]ATGAACTTTCTGCTT | 54467 |
rs77124214 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273058 | ACAGTATTTGCCACA[G/T]AACATTTTGGTCAAC | 54467 |
rs77160063 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92396879 | ATACTGTTTTGTGTT[A/C]ATGGAATATTTGTCT | 54467 |
rs77183379 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331773 | CACACCTCACTGTCA[C/T]GTGGCCATACCTAAC | 54467 |
rs77199509 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274807 | AAAAAAAATTTTTTT[A/T]AATTATCTACATGGG | 54467 |
rs77257621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390366 | TCCTGTAGCATTTAT[A/G]TCTTTGTTTTAAACT | 54467 |
rs77273698 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263154 | GAAATGACAGGAGGT[A/G]CATAAACCACAGGAT | 54467 |
rs77307551 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372261 | ACAGATTTTTTTTTG[A/T]AATTATTCCCTAAAC | 54467 |
rs77333472 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335721 | GCATTTGGTTCAGTT[A/C]TTTATCCATTCTGAT | 54467 |
rs77370033 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390145 | AATTACATTTAAATG[G/T]CAGCAGTTATTATGA | 54467 |
rs77390260 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306636 | CCTCTATGAGGAATG[A/T]GCCCTTACCAGACAC | 54467 |
rs77391522 | snp | C/G | 0.021333 | 0.101051 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290204 | ATCTTAGAAACTCAT[C/G]TGTTTGATTTCAACC | 54467 |
rs77406038 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282771 | GTTGAAAAGTCAAAT[A/G]TTTAAAAGCTGAATA | 54467 |
rs77413792 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388947 | TGAAGTATTGTCCAC[A/G]GTATAAATTGAGAGG | 54467 |
rs77485577 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92384736 | atacaaaaattaatt[A/C]acgatgcattaaaga | 54467 |
rs77518748 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344202 | TTTTTGGTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 54467 |
rs77547829 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306332 | GTCAACTACTAATCC[A/T]GTGACTCATTTTAGG | 54467 |
rs77585083 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278100 | AAAAAAAAAAAAAAA[A/G]GTTACCCAGGCATGA | 54467 |
rs77595174 | snp | A/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361827 | TTTGTTTTTTTTTTT[A/T]AAATGGAGTTTCACT | 54467 |
rs77614434 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358241 | AGCAAGACTCCGCCT[A/C]AAAAAAAAATGTGGC | 54467 |
rs77682873 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273059 | CAGTATTTGCCACAT[A/G]ACATTTTGGTCAACA | 54467 |
rs77817955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331688 | GGAAAGTTTTATGAG[C/T]CACTCCTGTAAGTGG | 54467 |
rs77823876 | snp | C/T | 0.260504 | 0.249779 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282468 | ACTTTTTGTGTCTGT[C/T]TTAGATGCATCAGCT | 54467 |
rs77831607 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364034 | TTTTTTAAGCCAGGC[A/T]CAATGGCTCACATCT | 54467 |
rs77948261 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92317839 | AGAAAATAAAAAGAA[A/G]CTACCATTTTGATCA | 54467 |
rs78014482 | snp | A/T | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92343753 | AAAATACAAAAACAT[A/T]TTTTATAATTTCTTG | 54467 |
rs78072165 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292313 | CAAAATGACTTCTCA[A/G]TGCCATTATCCTTTT | 54467 |
rs78092499 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92310272 | TGATGATTGTTTTCA[G/T]TTTCTGTATTCAGAA | 54467 |
rs78093411 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270821 | TCTTGCATTCAGCAT[G/T]ATACCTTTGAGATTC | 54467 |
rs78131902 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280267 | ATACAAAATGATTCT[A/G]TGAAAATTTCCTTTT | 54467 |
rs78193091 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380226 | GGTAAACAAAACGGC[A/T]GGGAAGCTCAAACTG | 54467 |
rs78247359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323689 | CAAAAGGTGAAAACA[A/G]CTCAAACGTTTATCA | 54467 |
rs78271763 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92373043 | TACAAAATAATTTTT[A/G]TAAGTCTGTATTACT | 54467 |
rs78314221 | in-del | -/AA | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278099 | CAAAAAAAAAAAAAA[-/AA]GTTACCCAGGCATGA | 54467 |
rs78392842 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275130 | TTGTGTATTTGTTTT[C/G]CAGTTTTCAAAATTC | 54467 |
rs78448677 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374876 | TAAGCTAACATAATC[A/C]AGAAAAAAAAAATGA | 54467 |
rs78453299 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293896 | GTTTATTGGAATAGA[A/C]TGAAACTAGCATTTA | 54467 |
rs78477316 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359088 | ATCCAGTTTTTTTTT[C/T]ATACTTAAGTTCTGT | 54467 |
rs78480597 | snp | A/G | 0.264906 | 0.249555 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92251931 | TTGTTATGTCTGTTC[A/G]TAGTTCTTCAGCCTC | 54467 |
rs78481257 | in-del | -/A | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269803 | GGTCTTTTTTTTTTT[-/A]AAAAAAATTATACTT | 54467 |
rs78482469 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92330896 | TAGCCCATAATAATG[C/T]TTAATAGTCATAATG | 54467 |
rs78520556 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389419 | TCAGATATTAAGGCA[A/G]TTTAGTCTTCCATCT | 54467 |
rs78709990 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380227 | GTAAACAAAACGGCT[A/G]GGAAGCTCAAACTGG | 54467 |
rs78727688 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357234 | TTAGATTAGGCAACT[A/G/T]TTTTTTTTTTCTTTA | 54467 |
rs78778291 | in-del | -/AG | 0.276267 | 0.248616 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345862 | AATACTATGTGGGTA[-/AG]AGAGCGAGAACCTGA | 54467 |
rs78783151 | in-del | -/C | 0.261884 | 0.249717 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362908 | CTCTGAGGGGACTCC[-/C]TTTTTAAAGCCTTCC | 54467 |
rs78809913 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284680 | ATTCATTCATTTGTT[A/C]CTTCTTTCTTTCTTT | 54467 |
rs78851004 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399375 | TCTAGAAATTTATTT[G/T]GGATAAATCCGATAA | 54467 |
rs78861811 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261461 | GCATAAATCCTTTCA[G/T]TCTCTCTAAGGTATA | 54467 |
rs78879697 | snp | A/G | 0.030278 | 0.119257 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387652 | AAAAAAAAAAAACAA[A/G]TATTGTTTTTCTGTC | 54467 |
rs78900083 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379626 | TACAACCAGTGGAGA[A/C]ACATGAGTTATTTAA | 54467 |
rs78902885 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356382 | TCTAGCTATTTAAGT[A/G]TCAGACTCCTGCCAA | 54467 |
rs78917742 | snp | A/C | | | missense, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92387996 | CAACGCCTTCTTAAA[A/C]CAGCCAAAGAAAAGA | 54467 |
rs79102128 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372259 | GTACAGATTTTTTTT[G/T]GTAATTATTCCCTAA | 54467 |
rs79102338 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344203 | TTTTGGTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 54467 |
rs79197878 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379427 | TATACGGCGGGATTA[A/T]GGGGAAGCAAGAATA | 54467 |
rs79306962 | snp | A/G | 0.0112701 | 0.0742163 | synonymous-codon, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92391201 | TGAAGACCTTGCCCA[A/G]AAAGTCAATAGGCCT | 54467 |
rs79368186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288888 | GAAACTGACAATTCC[A/G]ATTGCTGACCATGGT | 54467 |
rs79369627 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92341310 | GCGAGACCCTGTCTC[A/C]AAAAAAAAAAAAAAA | 54467 |
rs79422189 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282838 | TTATTTAGAGAGCTG[C/T]GATCATTATAGGTAA | 54467 |
rs79477786 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275426 | GGGGTGGTGCTGCCC[A/G]TCACCAACTCAGGAC | 54467 |
rs79488515 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313586 | TACAGGTATTGAAGA[A/G]ATAATTTTTTAATTT | 54467 |
rs79565048 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296040 | CTTTGGAACTTGATT[A/T]AAAAAACTTAACGTT | 54467 |
rs79568185 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273055 | AGTACAGTATTTGCC[A/C]CATAACATTTTGGTC | 54467 |
rs79583147 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92391151 | TGATTTTTTTTTTTT[C/T]TCTGCTTACTATAGA | 54467 |
rs79611211 | snp | G/T | 0.5 | 0 | downstream-variant-500B | ANKIB1 | GRCh38.p7 | 7:92402015 | CTCAAATATTTATCA[G/T]TTACGTGTTATGAAT | 54467 |
rs79669705 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379420 | CAGAAGTTATACGGC[A/G]GGATTAAGGGGAAGC | 54467 |
rs79706240 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296053 | TTAAAAAAACTTAAC[A/G]TTCAGCCTTTTTCCT | 54467 |
rs79736274 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268122 | GGGTCCTGAGAAGAT[A/G]CGTCAAGAAGGAAAG | 54467 |
rs79744085 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342857 | ATTTTGTGTAAAAAC[A/G]CTAATAACAAGAACA | 54467 |
rs79749467 | snp | A/G | 0.246485 | 0.249975 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282846 | AGAGCTGTGATCATT[A/G]TAGGTAATTGTGTTT | 54467 |
rs79851006 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380228 | TAAACAAAACGGCTG[G/T]GAAGCTCAAACTGGG | 54467 |
rs79868264 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264620 | TTTCTCCACATTGAC[C/T]AGGCTGGTCTCGAAC | 54467 |
rs79951488 | snp | A/T | 0.273104 | 0.249744 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303744 | GTTGGTAATTTAAAG[A/T]TTAGAACAAAAATTA | 54467 |
rs80006134 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370144 | CAAATTAAAAGATTT[C/T]AAGTGGTGTGTATTC | 54467 |
rs80007919 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365788 | GATATATTAAATAAT[C/T]TTTTTTTTTTTTTTT | 54467 |
rs80133818 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335913 | TTTAATTATCTGTTG[A/G]GTTTTTAGCTAATTC | 54467 |
rs80137103 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92324072 | AGGGGCAGGGAAGAG[A/G]AGGAGTGACTGCTTA | 54467 |
rs80168256 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274319 | TTAGAGCAGTAAGAA[A/G]TTTACACAAAATATC | 54467 |
rs80173855 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344209 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 54467 |
rs80174068 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289741 | GGGGGAATGAACAGG[C/T]TGAGAGCTTAGTATT | 54467 |
rs80193792 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279847 | AACCTTAGAGTCCAA[A/C]TTGACCCACTCAAAA | 54467 |
rs80202816 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380230 | AACAAAACGGCTGGG[A/G]AGCTCAAACTGGGTG | 54467 |
rs80225119 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305589 | ACAAAGAAAAGAGTG[A/G]CAAACTGAACTGGTG | 54467 |
rs80231664 | snp | C/T | 0.261056 | 0.249755 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92287209 | CTACTAACTAAACTA[C/T]TTACTGTGTTTAGAT | 54467 |
rs80272621 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353359 | GGAAAGGATATGTAA[C/T]TCTGAATACTCTTTT | 54467 |
rs111288792 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273292 | ATTCAGCTGAACTCA[G/T]ATAGGATGGATCAAG | 54467 |
rs111298506 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92254954 | TCCCGTGCTGTTCTC[A/G]TGATAGTGAGTAAGT | 54467 |
rs111304180 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380237 | CGGCTGGGAAGCTCA[A/C]ACTGGGTGGAGCCCA | 54467 |
rs111344907 | snp | C/T | 0.274929 | 0.248754 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92397316 | CATGGTGAAACCCTA[C/T]CTCTACTGAAAATGC | 54467 |
rs111372356 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311854 | GTCTCTGATGCCTAT[A/G]TCTGACTTCTCTGAA | 54467 |
rs111386545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92347819 | AATCTATAAAGTGGT[A/G]ATAATAGTATGTGCT | 54467 |
rs111390425 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357614 | GTGGTGCATACCTAT[A/T]GTCCTGGCTACTTGG | 54467 |
rs111404066 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383511 | ATACTGGCAAACCAA[A/G]TCCAGCAGCACATCA | 54467 |
rs111414202 | in-del | -/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273778 | TCTTTTTTTTTTTTT[-/T]GAGACAGGGAATCAC | 54467 |
rs111455045 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92249403 | CCACTTGACCCTGTT[A/G]CAAGGTTGTTTCATA | 54467 |
rs111636168 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92385862 | TTGTGCACATGTACC[C/T]TAGAACTTAATGTAT | 54467 |
rs111679375 | snp | A/C | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92250275 | GCACATGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 54467 |
rs111690666 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357723 | CTGGGTGCCAGAGCA[A/G]GACTCTCTCAAAAAA | 54467 |
rs111805492 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256928 | GGCTCTGTGGCTCAC[A/G]CCTGTAATCCTGGCA | 54467 |
rs111882166 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319314 | GTTGCAAGTTTTTGA[A/G]AAAAAACTTTTTTAG | 54467 |
rs111946649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92348151 | CTGTCTTCAATGAGG[C/T]CTTCTCAGTTCTGTA | 54467 |
rs111947127 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247578 | TTTCAGATTTTTGAA[C/G]TAGGCGTTTTTTCTC | 54467 |
rs111983677 | snp | A/C | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278453 | AGGAACCCTTCCAAA[A/C]ACAGTTCTGAAAAAC | 54467 |
rs111989638 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92261422 | TTGTTTTGTTTTGTT[G/T]TGTTTGGCAACATAC | 54467 |
rs112003803 | snp | A/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92363055 | TAGTTCTGGTCTTTA[A/T]AAAAAAAAAAAGACT | 54467 |
rs112016909 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92363277 | TTAGCTGGGCGTGGT[G/T]GCACGTGCCTGTAGT | 54467 |
rs112020434 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | ANKIB1 | GRCh38.p7 | 7:92402026 | ATCATTTACGTGTTA[C/T]GAATTAAAATCTGGA | 54467 |
rs112074989 | in-del | -/GT | 0.347089 | 0.230377 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290371 | AGTATATGTATGAAA[-/GT]GTGTGTGTGTGTGTG | 54467 |
rs112207870 | in-del | -/CTC | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387085 | TTCTTGATGAGGGTT[-/CTC]CTCTTGGTTTGCAGA | 54467 |
rs112248140 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92259047 | TAACCTCTGCTTCCC[A/G]GGCTCCATTGATCCT | 54467 |
rs112253892 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92299159 | AGCTTTCAAGTGATT[A/G]TTAAAATCCAGGAAA | 54467 |
rs112360738 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353721 | AAGGTTCAGCAAACT[A/G]TTGTCTATACTTATT | 54467 |
rs112394025 | snp | A/G | 0.26078 | 0.249767 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309818 | TAGTCCCAGCTGCTT[A/G]GGAGGCTGAGGCAGG | 54467 |
rs112466383 | in-del | -/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92347280 | ACATTATGAGTTTTT[-/G]TTTTGTTTTGTTTTT | 54467 |
rs112514798 | snp | G/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92254404 | ATTTAATTTTAATAC[G/T]TAATGCTAAATTATT | 54467 |
rs112516041 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312092 | TTTTTTTAAATTGCA[C/T]CAAACTCATACTACC | 54467 |
rs112516651 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387615 | CACTCCAGCCTGGGA[C/G]ACACAGCGAGACTCC | 54467 |
rs112523891 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307809 | TAAATAAAGGGCCTC[A/T]TTTTTTTTTTTTTTT | 54467 |
rs112620589 | snp | A/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338935 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 54467 |
rs112621068 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366842 | CATCTGGTATCAGAA[G/T]GCAGAAAAACTCTTT | 54467 |
rs112671222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361376 | AGGTAAAAGTAACTA[C/T]AGTAATTCAACTTAA | 54467 |
rs112682485 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256001 | AAACATTTAATTATA[A/G]TTTTAGATGGTAAGT | 54467 |
rs112686248 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247761 | AATTTAAGAATAATT[C/T]TACTGTGTACTGCAG | 54467 |
rs112703793 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339303 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 54467 |
rs112804084 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92381160 | TTGAAGATCAAATTA[A/G]TGAAATGACGCAAGT | 54467 |
rs112882706 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270119 | CCAAGCTGGAGTGCA[A/G]TGGTGTCATCACAGC | 54467 |
rs112902395 | in-del | -/A | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387480 | ATCTCTACTAAAAAT[-/A]CAAAAATTACCCAGG | 54467 |
rs112950283 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291672 | AGCTCCACCTCCCAG[A/G]TTCAACCAATTCTCC | 54467 |
rs112952692 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92324379 | GCTGGGATTACAGGC[A/G]CCCACTGCCACACCT | 54467 |
rs112964646 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344500 | GTGAGCCACCGCGCC[C/T]GGCCTAATACTTAGT | 54467 |
rs112972249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289624 | TTCCCACTCTGGCCT[C/T]GTTCCCCTTAAGACC | 54467 |
rs112988701 | snp | A/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333941 | TGCCTCACATTTTTT[A/T]TATGTGACACATTTT | 54467 |
rs113067234 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92302044 | AGGGTTCAAGCAGTT[C/T]TGCCCCAGCCTCCCA | 54467 |
rs113107513 | in-del | -/TCT | 0.261884 | 0.249717 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92360843 | GAGTCAGTTGGTGTG[-/TCT]TCTTAACACACATAA | 54467 |
rs113236981 | snp | C/T | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380593 | CTGTTCTGCAGCCTC[C/T]GCTGGTGACACCCAG | 54467 |
rs113270132 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92359957 | TCTGTTAAGCTACCA[C/T]TAAGTTGCTAGGAGC | 54467 |
rs113346200 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92250191 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 54467 |
rs113444442 | snp | A/T | 0.030278 | 0.119257 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296752 | GTATTTTACACAGAG[A/T]AAATAGAAGTTCTAT | 54467 |
rs113478410 | in-del | -/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264574 | ACTAATTTTTTTTTC[-/T]TTTTTTTTTGTATTT | 54467 |
rs113502259 | snp | C/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264829 | ACTTATAACCTAGTA[C/G]AATAGACAAACACTA | 54467 |
rs113531752 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92246255 | GGCCGGAGAGGGATG[G/T]GGGGCGCCCACCCAG | 54467 |
rs113565806 | in-del | -/A | 0.272241 | 0.249009 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374879 | GCTAACATAATCAAG[-/A]AAAAAAAAATGAAGG | 54467 |
rs113626950 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390554 | AAACACCTAAGCCAA[G/T]TGGCATCACTATAGC | 54467 |
rs113685435 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282222 | TGAGTGGCGCCATCT[C/T]GGTGCACCACACCCT | 54467 |
rs113713986 | snp | C/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353699 | TGCAAACCCCTGACT[C/G]TAAGTCAAGGTTCAG | 54467 |
rs113743168 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92347481 | ATAGTGGCACATGTC[C/T]GTAGTCCTAGCTACT | 54467 |
rs113772145 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323274 | CACATTCTTGCTAGC[A/G]TTGAATATTATCAGT | 54467 |
rs113774200 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280093 | CTGATATTCAGAGTG[C/T]TCTGCTCACCAGTAG | 54467 |
rs113800464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269996 | AGTGTGTGAGTTCCC[C/T]GCCCTGTGTCCAAGT | 54467 |
rs113801862 | snp | A/G | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92259935 | TAAGAATTCACCACC[A/G]TCACTGCTACCTCCT | 54467 |
rs113866114 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92281275 | ACCTTCTAACTAGCA[C/T]GTACCAATATTCCAG | 54467 |
rs113875070 | snp | C/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92332257 | ATGCTTGTGAGTTAG[C/T]GCACATAACTACAGT | 54467 |
rs113893401 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307084 | TATATTTCTCATCTT[C/T]CTTTTTTCTTCCTTT | 54467 |
rs113924455 | snp | G/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305439 | CTGTGTTTGTGACAC[G/T]GTGTTGGGGATTCAA | 54467 |
rs113928184 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390704 | ATCAGTATTCATTTT[A/C]TCCGTAAAGCCTTCC | 54467 |
rs113967798 | snp | C/T | 0.5 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285334 | CTGGGAAGATTTAAA[C/T]GTAGTTCTTTCTAGT | 54467 |
rs113984994 | snp | A/C | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311728 | AAGCGCCCCCCCCAC[A/C]CACACACACACAGAA | 54467 |
rs114020344 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361366 | GGAGATGCAGAGGTA[A/G]AAGTAACTACAGTAA | 54467 |
rs114085029 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92260699 | AAAAAAAAAAAAAAG[C/T]CATTTTGGTAAGGCT | 54467 |
rs114236272 | snp | C/T | 0.0448719 | 0.142907 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247801 | CTGCAAACTACTGTG[C/T]AGTGTAGACTGGTAG | 54467 |
rs114373901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395060 | ATGGAAAGACACCAT[A/T]ATGATTCTCTAAATT | 54467 |
rs114427523 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378477 | TGCTGAAAAGCTATT[C/T]GACAAAAAAAAAAAA | 54467 |
rs114464989 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270783 | ATAGAATCATATAGT[A/G]TATAGCCCTTTGAGA | 54467 |
rs114669641 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323744 | TGAGATATACACACA[A/G]TAGAATATTACTCAG | 54467 |
rs114722800 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289215 | GATTTATGTATCAAC[A/G]TGGATAAATCTTAGT | 54467 |
rs114752180 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283030 | GCTATTTTCATTTCT[G/T]CTCTAACTACAGTAT | 54467 |
rs114793995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92360093 | TTTTTTACCATGTAA[C/T]CATTTTTAAGTATGC | 54467 |
rs114801083 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366603 | AGTCTTTTGTCTCCT[A/G]TCATGTTTTCAAACA | 54467 |
rs114888110 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356842 | AAATAGTACCAGTTA[A/C]AAAGAGATGTTAAGA | 54467 |
rs114925809 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395418 | TCATTTGATTTGTGA[A/G]TATGATATGTAGTAG | 54467 |
rs114957191 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92325116 | ATTAGACCTAGGTTG[A/G]GGTCAGATTCTGTAG | 54467 |
rs115012495 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247419 | AGACAGACGTTTAAA[G/T]ATCATATTAGATTGT | 54467 |
rs115094140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372072 | AGCTGGTTTTGGAGC[A/G]TACGGCTTAGACTCA | 54467 |
rs115153871 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315424 | CATAGAGTTGACAGC[C/T]AAAAGCAAGATAATG | 54467 |
rs115227892 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375527 | AACAACTTCTCCCCA[A/G]TTCAAGTTTTATCAT | 54467 |
rs115235205 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319921 | GCCTGGCGACAAAGT[G/T]AGACCCTGTCTCTAA | 54467 |
rs115235242 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263563 | CAGATTTGGTAATAT[C/T]TCTGGGGTAGCTAAG | 54467 |
rs115330733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92310783 | TGACAAGAAAAAAAC[A/G]TGGATGTTCAATACA | 54467 |
rs115333923 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256927 | AGGCTCTGTGGCTCA[C/T]GCCTGTAATCCTGGC | 54467 |
rs115339242 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362476 | ATCATGGACAAGTTC[C/T]ATGTTTCTAACAGAC | 54467 |
rs115340325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92304279 | ATGCAGATATGCTAC[C/T]GTGTCTAATAATTTG | 54467 |
rs115350745 | snp | A/C | 0.268343 | 0.249326 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288841 | CCATTATAATGGCTA[A/C]CAAAAAAGAAAAAAA | 54467 |
rs115502034 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365359 | AAGCTGATAGATGTC[C/T]TTCACATGAACCAGA | 54467 |
rs115595927 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92376782 | TATGAAGATGGCATC[C/T]TTCCTTAAACCTCAT | 54467 |
rs115849705 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92317445 | TAAGACCTTGCCCTC[A/G]GAATCTAGAAGGTGG | 54467 |
rs115861035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92365399 | ACATTCCAGGCATAG[A/G]GTGAAGTGGCAATAT | 54467 |
rs115868470 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92390553 | AAAACACCTAAGCCA[A/G]TTGGCATCACTATAG | 54467 |
rs115895410 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321655 | CTTGATTCTAAAAGG[C/T]ATTATGTAACTACTG | 54467 |
rs115899827 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264483 | GCTCACCACAACCTC[C/T]GCCTCCCAGCTTTAA | 54467 |
rs115976149 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379676 | GCAGTTGTGTGAGAA[A/G]GAATAAAGTTGAATT | 54467 |
rs116035131 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323906 | AACAGATAAAAGCCA[C/T]AGAAACAGAACTCAT | 54467 |
rs116154112 | snp | C/T | 0.0225045 | 0.103662 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401545 | TTACTGAGCATTTTA[C/T]ATCCCAGTTATAAAT | 54467 |
rs116167364 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92287470 | TTTCACAAGAGTACT[A/G]CAGAACTTATGTGCC | 54467 |
rs116270312 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255412 | GGAGCTGGTATAGTG[A/G]TTCCACAGTGCTATC | 54467 |
rs116300760 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92377459 | AAAGTTTGAAACATT[A/C]TGAGAATTACCAAAA | 54467 |
rs116300913 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282627 | TACTAAAATTACACT[A/G]TTTGCCAACAGCACC | 54467 |
rs116312145 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358933 | CCATATGGAAACACT[A/G]TTCCTAGATCTATGG | 54467 |
rs116324707 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92341377 | TTTTCTTTTAAAAAC[A/G]CAATGGGCCTTAGAC | 54467 |
rs116379258 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290717 | GTTAATTTAAGTACC[A/G]TTGAGTTTTTGTTAC | 54467 |
rs116386283 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92273970 | TAGAGATGAAGTCCC[A/C]CTATGTTGTCCGGGC | 54467 |
rs116397232 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92349270 | GGAAGAAAGGAAAGA[A/G]TGCTAAAGATACTGC | 54467 |
rs116474607 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92286397 | AGTAAATAGCATTGA[C/T]TTTTCTTGGTGTGGC | 54467 |
rs116485271 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266213 | AGAGGGCTGCTAAGA[A/G]TTCAGATAGGATGAG | 54467 |
rs116492966 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354943 | TACAAAAACAACAAA[C/T]GACAATAATAATTTC | 54467 |
rs116540920 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338497 | GTTATGTGTATATAA[C/T]TGTTTTTAATAATTC | 54467 |
rs116699711 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374962 | CAGAGATGCTGTGGT[C/T]CAGTTCCAGACCACT | 54467 |
rs116712572 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336559 | TTAGAGTATATTGCT[G/T]TAGGCATTATATGTA | 54467 |
rs116766050 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329492 | TGAGAAACATTGCTG[C/T]GCATATTTATCTCAT | 54467 |
rs116794731 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282929 | AGTTTCGACAGTTTT[C/T]TGCTTGTAGACCTCA | 54467 |
rs116865086 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374377 | CAGCTACTAGGGAGG[C/G]TAAGGTAGGAGTGTC | 54467 |
rs116875932 | snp | A/G | 0.00394587 | 0.0442421 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92246544 | AGCTTCGCGGTACAG[A/G]TGTGTTTGAGGCTGC | 54467 |
rs116891782 | snp | A/G | 0.025748 | 0.110504 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92352452 | AATATTTTCTTTTGT[A/G]TTTTGTTATTGCTGT | 54467 |
rs116915150 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277445 | AACCCCATCATAAGT[C/T]GAGGAGCATCTGTAT | 54467 |
rs116993975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290759 | CTATCAATGGTGCAG[C/T]TGGGAGACAGAGATT | 54467 |
rs117010573 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321405 | TTTTTCATAGGACCT[A/G]TCACATGCTATAATT | 54467 |
rs117011767 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92270507 | TTCAGGTAGTAGAAG[A/C]AAACTTTTATTTTTT | 54467 |
rs117012444 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266101 | GAATCTGAGAACCAG[A/G]TGTCCAGTGAGGTTG | 54467 |
rs117056067 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92346915 | ATTATTGGTTTCCTT[A/T]GTACCTTCTAGCCTA | 54467 |
rs117144480 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92396581 | TGTCATTTAGATATA[C/T]AATAAATATGCAGAT | 54467 |
rs117169559 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245107 | AGATCCTGAGTTGGA[C/T]CACCGAGATGAAAGA | 54467 |
rs117223959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92286011 | GAGGTTTTATAGAAG[A/G]TAATTTAATGACTAC | 54467 |
rs117258920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245430 | TAAACTCCTTGCCTG[A/G]GGCAACTAGATGTGG | 54467 |
rs117279682 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340093 | CTCTTTATTTGGCCA[C/T]TGAATTTTTTTTTAA | 54467 |
rs117286808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388305 | TTTGCTTACTCTGTG[A/T]CACTGCTGATGCTCT | 54467 |
rs117331233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277249 | AGCACTGTGAAAATG[C/G]ACTAATACAGTACTC | 54467 |
rs117364263 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92368479 | CCCAGTACTTGGAGA[C/G]GCCAACGCAGGCAGA | 54467 |
rs117367439 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264071 | CCATTGTATGATTAA[C/T]CATCACTTATTTTAT | 54467 |
rs117370502 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92337508 | ATTTCTTTCCTAATG[A/T]TCAGCTGTTCTTATA | 54467 |
rs117376527 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92249980 | TCTCGAAAAGATTTG[A/G]CTTACAGTCCTTAAA | 54467 |
rs117392323 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92350638 | CAAGGCAGGAGAATC[A/G]CTTGAGACCAGGGGT | 54467 |
rs117405506 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313793 | ATCTCTGGGAATAGA[C/T]TCCAGAAATGTTTAG | 54467 |
rs117418444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361731 | TCATTTTTAGTGCCT[C/T]CATTGAAATGCTCCA | 54467 |
rs117444970 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314358 | TGAAAGCAAATATGA[G/T]GAGATTAGCCTGATG | 54467 |
rs117453488 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258521 | TTGCTGTTGTCTTTT[A/G]TATGAAATTAATTTG | 54467 |
rs117498668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92331725 | TCACTCCTGTACGTA[C/T]TTCATTCATTGACCA | 54467 |
rs117527070 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339383 | AACCATGTGAACCCT[A/G]TACTTTTTAAATAAA | 54467 |
rs117547960 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92287080 | TTAAGTAATTTTAGA[C/T]TTATGGAAAGGTTGC | 54467 |
rs117551793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275732 | CAGCTTCTTTCCTCC[A/G]CTTAGCCTAAAGGAA | 54467 |
rs117613084 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357193 | ATGTTAGGTTAACCA[A/G]TCATATTTGAGCTAC | 54467 |
rs117613526 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372818 | ATGATATTCTGATTT[G/T]TTTTGCTTTATCATT | 54467 |
rs117630786 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289281 | AGATCAAGCTTAAAA[A/G]CCTGCACACAGAATA | 54467 |
rs117658538 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268105 | GTTTATGAGCTAAAG[A/T]TGGGTCCTGAGAAGA | 54467 |
rs117685469 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264450 | TCACCCAGGGTGGAG[C/T]GCAGTGGCGTGTTGT | 54467 |
rs117704951 | snp | A/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247171 | GGAATGGCATATCGA[A/T]CAATCTTGTATTGGA | 54467 |
rs117709660 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92271990 | ATGATTTCATGGAGA[G/T]AGAAAATGGAATGGT | 54467 |
rs117733150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92251469 | ATCACTAGATGTTCT[A/G]TATCACATCTTTATT | 54467 |
rs117791130 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268340 | CAGGTAAATAAAATT[A/G]GAATATAATGGAAGA | 54467 |
rs117795543 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294808 | TGATTCCCAGATTTT[G/T]TTTAGTGTTCCTAAT | 54467 |
rs117834210 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364723 | ATTTATCCTCCTAAT[A/G]GAATAAGCCATAAAG | 54467 |
rs117901457 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292880 | TTCTTGCAGTAAACC[A/G]TGAGGTAAACCATGA | 54467 |
rs117907311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92324583 | AAAACTTATATTTGT[A/G]CCTTCTACTTTGACC | 54467 |
rs117939028 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305387 | TGAAAGTTTAATATG[C/T]ATCCAATTCATTTAT | 54467 |
rs118003854 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315363 | AAAGTGTTAGGGAAT[A/G]AAGAATATAGACACT | 54467 |
rs118013431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280987 | GATTCCCTTAGAGAA[C/G]TCACAGGACTCAGCG | 54467 |
rs118030488 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284248 | TAGTAATAGGATGAA[G/T]ATAATGAGGCATGTA | 54467 |
rs118057251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92267378 | AAGCCTTCCCTCATC[C/T]ATCCAGTAAAAATTA | 54467 |
rs118087187 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92327539 | AACTAGTACAATGCA[A/C]ATAATATGTAATTAG | 54467 |
rs118109716 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92310343 | GGAGCCCTATAAATA[C/T]CTTACATTTATTCTA | 54467 |
rs118111016 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288472 | ACACACAGAAAAATA[A/G]AACACAGTCAATTGG | 54467 |
rs118136766 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92341736 | TAGTCCCTGACTTAG[C/G]ATGGTTTGACTTACA | 54467 |
rs137907206 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92370081 | ATCATAATAGGCTTT[A/G]TATTCTTTGCAAAAG | 54467 |
rs137945265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378105 | CTCTACAGATATTAG[C/T]AAACATAATCCAGCA | 54467 |
rs137945313 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313875 | AGGTCTCAGACATAC[A/G]CAGATTGAAGTATTT | 54467 |
rs137983408 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92267648 | TTACCTTTCACATAT[A/T]CATCTGCAGTTCATC | 54467 |
rs137985176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92318303 | GGTGGATCACCTGAA[C/G]TCAGGAGTTCAAGAC | 54467 |
rs138014108 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303624 | AGTAGAGCCATCATC[A/G]TGGGTAAAAGAGAAG | 54467 |
rs138029500 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362962 | ACAGAGAAATCTATC[G/T]GCTTTGCAATAATTT | 54467 |
rs138032462 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400155 | GCTTTTACACTAACT[A/G]TAACAACTAAATGTT | 54467 |
rs138051513 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345513 | CAGAGTTAAATGTTT[C/T]AGCGAGACATAGTTG | 54467 |
rs138054046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308966 | CTTAATGTTGTTCAT[A/G]TATACTTTAGACTTC | 54467 |
rs138103370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255337 | GAAATCCAAAAAAGG[G/T]TCATATAAATAAACA | 54467 |
rs138137303 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92259721 | AATGTAACTTGTTCA[A/G]ATATAAGCAGATTTT | 54467 |
rs138166930 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92300350 | TCTACCAAAAGTCTT[C/T]GGATATTTTCTTTTT | 54467 |
rs138171934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388468 | AGGGCGTGGAAGTCA[A/G]TAACAGTTTGGGAAG | 54467 |
rs138195075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283817 | GCTCTGTTTCCCAGG[C/G]TGGAGTGCAGTGGCA | 54467 |
rs138270457 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383798 | GATACTGAACGGGCA[A/G]AAACTGGAAGCATTC | 54467 |
rs138287648 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292415 | AATGAGTACTCCATG[A/G]TAACATTACTTTCTT | 54467 |
rs138293714 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92391846 | TTATTTTACATACTC[A/T]TACTACTTCTGTAAA | 54467 |
rs138302149 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378373 | GGGATGCTTCCACCT[A/G]TATAAGAATGGTTCA | 54467 |
rs138314345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278974 | AGCAGTGGTCCCCAA[C/G]CTTTTTGGTACTAGA | 54467 |
rs138364331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245251 | GACAAGCTGTGAATC[C/T]CTTTCCCTGCAATGA | 54467 |
rs138366048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344088 | TTCTAGAGAGCTATT[A/G]TTTAGAAGATACTAG | 54467 |
rs138404649 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92327489 | ACCTATGCATATCCT[C/T]CCATATACTTTAAAT | 54467 |
rs138404715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387302 | TATTAATTTTAGGGG[A/G]AATACCATTAGTCCA | 54467 |
rs138426711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369298 | AGTAAAGTCTGATCA[G/T]TTCATTACCGCTGTT | 54467 |
rs138437092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333702 | CCCGCTACCTGACAT[A/G]GTGGATGGGACATAA | 54467 |
rs138465089 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313173 | ATTCAGCTGTGCCCT[A/G]CTTGCTTATTCAGAG | 54467 |
rs138596344 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92393024 | TCCATCCTTGCTCTT[C/T]ATTAAACAGTATTTG | 54467 |
rs138609846 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293679 | TTTAATTATCTGTTC[A/T]TTTCAGGTTAAAGTG | 54467 |
rs138651285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92320507 | TCCTTTATGTCTTCC[C/T]GGTCTCAATAAATAT | 54467 |
rs138669802 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92353403 | TCAGCCATCAGCACT[C/T]TACTTATTCATAGAA | 54467 |
rs138683885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92325574 | TTCTCCCTGAACATC[G/T]AAACATCTTTTAAAC | 54467 |
rs138687172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268100 | GTTTTGTTTATGAGC[C/T]AAAGATGGGTCCTGA | 54467 |
rs138688468 | in-del | -/CT | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386017 | CTCATATTTTTGGCA[-/CT]GTCTGATAATTATGG | 54467 |
rs138703644 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274109 | TTAAGCTTTTCTGTT[G/T]CCAGTCAAGAATTTA | 54467 |
rs138745913 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92254032 | CAGCTGAGTGTGAGG[A/C]AGCTGGTCTAGTGTA | 54467 |
rs138760175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335065 | TTTTTGTGATTTGTC[A/G]TTCATATCTTTTTTA | 54467 |
rs138929014 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92326230 | TAAAAAACTGGATCT[A/G]TGCAGATTGTTTCAT | 54467 |
rs138948742 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274857 | GCCCGAGCCCAGGAG[A/G]TGAAGACTGCAGTGA | 54467 |
rs138959488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279200 | TAATGTTCACTTGCC[C/T]GCTGCTCACCTCGTG | 54467 |
rs138978086 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283204 | TGTGTTTATGTAGCC[A/G]TTTTATTTGGAATGC | 54467 |
rs138979645 | snp | A/T | 0.106278 | 0.204558 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383283 | GAGTCCAGGACCAGA[A/T]GGATTCACAGCCAAA | 54467 |
rs139023078 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344246 | TTTCACTCTTGTTGC[C/T]GAGGCTGGAGTGTAA | 54467 |
rs139036532 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311408 | TAACACAAATTCTCT[A/G]TTAGCCTGTTATTGC | 54467 |
rs139053135 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92256793 | TAAAATGATTTTCAA[C/G]TTGGAATACCAAGTA | 54467 |
rs139063706 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92351432 | TTTTACCTACTTTAA[A/G]TTTTCCAAAAGACAT | 54467 |
rs139071017 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92346689 | TCTTAGTTGTTAACT[C/G]TACTTAATTAGGAAG | 54467 |
rs139104059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291697 | TTCTCCTGCCGCAGC[C/T]GCCTGATTAGCTGGT | 54467 |
rs139111260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354061 | ACTGTGGTTTCTGTG[A/G]TCTAGCTTTTACCAG | 54467 |
rs139111336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290222 | TTTGATTTCAACCTG[A/G]AGTGGGATGGGGTTG | 54467 |
rs139149262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294271 | AAAGAAATAAATTTA[A/G]TGGTCTTAAATGGTA | 54467 |
rs139165115 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248160 | AGTCTTAGAAAAAAT[A/G]TTGTTGATTCTCTTT | 54467 |
rs139178991 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92330181 | AATGGGTCTATTCCT[A/G]TTTTATTCCATGCAT | 54467 |
rs139253127 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92276192 | GATTCTAGGCCCAAG[G/T]CATATTTATTTTCAA | 54467 |
rs139308269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366034 | TCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 54467 |
rs139314397 | in-del | -/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92307808 | TTAAATAAAGGGCCT[-/C]TTTTTTTTTTTTTTT | 54467 |
rs139348711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366865 | AACTCTTTAAAGCAA[A/G]TATTTTTAAATAGAT | 54467 |
rs139358405 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268856 | GCTTGCATCTCATCT[A/G]GCTGTACCTTACGTT | 54467 |
rs139460925 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358502 | TCTTGGAGAGCCAAG[A/C]ACATTGATAAGCAAT | 54467 |
rs139480347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92304690 | TTTTTGTCAATCATG[C/T]CTTGTAGAAGAGATA | 54467 |
rs139490587 | in-del | -/T | 0.124144 | 0.21601 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264564 | GACTAATTTTTTTTT[-/T]CTTTTTTTTTGTATT | 54467 |
rs139491136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92376391 | TAGATCTTCTGGATA[A/C]TTTGCCACAGCTTCT | 54467 |
rs139495557 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284702 | TCTTTCTTTTCTTTT[C/T]TCACATAGAGAAGTA | 54467 |
rs139530461 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315618 | TACAATGTCAAAGAT[A/G]CAAGAGAAGAATTTC | 54467 |
rs139531722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379631 | CCAGTGGAGAAACAT[A/G]AGTTATTTAAATGGT | 54467 |
rs139568649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321656 | TTGATTCTAAAAGGT[A/G]TTATGTAACTACTGG | 54467 |
rs139599941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379915 | GTGGGTGCAGCACAC[A/G]AAGGGCAAGCCGAAG | 54467 |
rs139640743 | in-del | -/GTTGG | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264181 | TTTTTTTGTTTGTTT[-/GTTGG]TTTTTTTTTTTCTGG | 54467 |
rs139672123 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92250418 | AATCAATAAAGCAGA[-/T]TAATTATATACTATC | 54467 |
rs139689632 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92322700 | TCTCCTAAGTCAGAA[C/G]ATACAATCTACATAT | 54467 |
rs139697873 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284119 | TAACATTTCAATATA[A/G]TATTTGTGACATTTA | 54467 |
rs139734079 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289082 | GTTATGGCAGCCTTA[A/G]TAATAATTGCCCCAG | 54467 |
rs139805322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395237 | ATTGTCACAAATGTG[G/T]AATAGGCTGAGGACA | 54467 |
rs139824665 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400418 | ACTAGCATAACATAA[G/T]CAAAATAGATAAGTA | 54467 |
rs139845849 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345997 | TATACAAGCTTGAAA[A/C]CATCACCACAACCCT | 54467 |
rs139848142 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248812 | ATGGTAATTTTTGGA[G/T]TCTCAGTTTATTTTT | 54467 |
rs139878181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314430 | AGTGTTTCTTAAAAG[C/G]CTTGCTACTCAAAAG | 54467 |
rs140033908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269604 | CCTGTTGCCCTGTTA[C/T]AGACTAGAATTATTC | 54467 |
rs140052653 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275877 | AGCATCACTGTACAT[A/G]TCTCTTTGTGTACCT | 54467 |
rs140056062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375192 | TTGCTGATGGAGAGC[C/T]TTGCCTCAGTGTTGA | 54467 |
rs140075998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92325598 | TTTAAACTTTTAACA[C/G]TTACAGTTACTTTTG | 54467 |
rs140141110 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314212 | CTGAGGTGGAAGGAT[C/T]ACTTGAGCCCAGGAG | 54467 |
rs140145117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92257711 | GCAGGAGAATCACTT[G/T]AACCCTGGAGGCGGA | 54467 |
rs140223981 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284974 | TTTTAGGTATCTAGC[A/G/T]TAGAAGGTAATTATT | 54467 |
rs140283485 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92317660 | GTCAAATCCAGTGGG[C/T]TTGTCAAGTTAGCCC | 54467 |
rs140292210 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263055 | CATAATTTTCTCAAT[A/T]TACTATAAGGTCTTT | 54467 |
rs140311304 | snp | A/G | 0 | 0 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92267408 | ATGTCTCCCAAGAGT[A/G]ACTATTATCATGACT | 54467 |
rs140343417 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362057 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 54467 |
rs140440454 | in-del | -/AT | 0.0240643 | 0.107019 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264848 | AGACAAACACTAAAC[-/AT]ATAAATACATCAAAT | 54467 |
rs140446649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92368349 | GAAGTGAAGAGAAGA[G/T]TTTGAAAGTCAGTAG | 54467 |
rs140448266 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308743 | TCACTACTATACATA[A/C]AACAGAATAGGTTTT | 54467 |
rs140448819 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356370 | AGATTGGCAGTATCT[A/T]GCTATTTAAGTATCA | 54467 |
rs140457592 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258999 | CGTTTTATTACCCAG[G/T]TTGGAGTACAGTGGC | 54467 |
rs140488131 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312161 | TCCATTTATTTCTGT[C/G]GCCACTTTCTAACAC | 54467 |
rs140521347 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335794 | TTGGATTTAGGTCTT[C/T]CATTTCACTGTTTGT | 54467 |
rs140561851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92348626 | CCTGACCTTGTGATC[C/T]GCCTACCTCGGCCTC | 54467 |
rs140562308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339825 | TTTTTTTCTTGCAGT[G/T]TATAGGTTGTCTATC | 54467 |
rs140582588 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290788 | TTTGAAGCTAGAATT[A/T]TACACTTATTTGTGG | 54467 |
rs140641084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92332992 | GCAGCACCAGCCAAC[C/T]AACTGGGTATTCGAG | 54467 |
rs140665362 | snp | A/G | 0.0003134 | 0.0125141 | synonymous-codon, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92386562 | GAAAAAACATAGTTC[A/G]TCCACTGGAGGTTAT | 54467 |
rs140681825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92278480 | AAACAAATCATTTCC[G/T]ATGCCTCCCTAGGTG | 54467 |
rs140739631 | snp | C/T | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92389998 | GTCCAGATACCACTT[C/T]CATTGAAGATGCAGT | 54467 |
rs140763836 | in-del | -/GTTG | | | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293362 | GTTGTTGTTATTGTT[-/GTTG]TTTGTTTTGAGATGA | 54467 |
rs140775876 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92337381 | TTTTCTTACTATTTA[A/G]GAGCTCTCTTTTTAA | 54467 |
rs140817886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92272523 | AGGTAGGAAGATTTA[A/G]CCTAAGACTGTACAG | 54467 |
rs140819102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92368923 | AAGAAAAAACTGTTA[C/T]GTTGCAGGCCACACT | 54467 |
rs140871385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ANKIB1 | GRCh38.p7 | 7:92397999 | TGTGCTGCAGGAAAA[G/T]ATATTCCTATATTTT | 54467 |
rs140895489 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354603 | ATCTTTTGTCTTTCA[A/G]TTTTGGTATTTATTA | 54467 |
rs140927415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361478 | GTAAATCACATGGGG[C/T]CTGTTCTTCTGCATG | 54467 |
rs140948993 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306776 | GCAGATTAAGACATC[A/G]TGTAAATATATGCCT | 54467 |
rs141006387 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92387402 | CACTTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 54467 |
rs141023555 | in-del | -/CA | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279877 | AAACAAACAAACAAG[-/CA]CACACACACACATAC | 54467 |
rs141029733 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312759 | TAACAGGTCCTATAA[A/G]CTTCAGTTATACAAA | 54467 |
rs141051459 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296118 | GCTGCTTTTTTTGCT[A/G]TCTCCAAAACATGCC | 54467 |
rs141067534 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92260181 | TAAGACCCTACCTAC[A/G]CAGTTGCCTGCCCCT | 54467 |
rs141068975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92316386 | TCCTGACTTTATGCC[A/G]TAAAGGTCAGCAAGC | 54467 |
rs141126241 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92369618 | TTCAAACTGCAAGGG[G/T]TCTGATTTCTCTCCT | 54467 |
rs141150618 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92310176 | CAATTTGCTTGATAC[A/G]TATGTGTGAGCATGT | 54467 |
rs141186059 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277463 | GGAGCATCTGTATTA[G/T]TCAGGCAGTCCCCAG | 54467 |
rs141230826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255791 | TTAAAGTTATTTATA[C/T]GCAAACGGAAATAAA | 54467 |
rs141263450 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92399916 | CAATTACTTTTAATC[A/G]TGTTTTATAAAATAG | 54467 |
rs141328169 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92281310 | TCTGAAGAAAAGCAG[G/T]TGATTAGCATATACT | 54467 |
rs141353355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92337937 | AATAACTGAAAAAAA[A/G]GGAGGAGATCATAAA | 54467 |
rs141385916 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92247691 | GATTGGACAATAGCT[C/T]TTATATGACTTTATG | 54467 |
rs141396916 | in-del | -/A | 0.228842 | 0.249103 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361669 | TAAATGAATGTACTG[-/A]TTTTTTTTTTAATAA | 54467 |
rs141471559 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282932 | TTCGACAGTTTTCTG[C/T]TTGTAGACCTCATGC | 54467 |
rs141471656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342568 | AGCTGTTTATTAAAT[G/T]ATTTTTAGGACCTGT | 54467 |
rs141481397 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401026 | GTACACAATGGGTTC[C/T]GGTTTCCTTGCACCT | 54467 |
rs141493434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338181 | TTGGGGAGCCAAGGC[A/G]AGAAGATCACCTGAG | 54467 |
rs141502650 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321617 | TCCCAAAAGGATTCT[C/G]ATTCCTCAGTGTTTA | 54467 |
rs141527259 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268676 | AGACCAGCTTTCACC[A/G]TGTTGCCCAGGCTTG | 54467 |
rs141564096 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92292224 | GACCGTTTAGATGAT[A/G]CATTTCTTAGTGACT | 54467 |
rs141633106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92262579 | AAGATTCCAAGTATA[C/T]AGCATGATCTGGTTC | 54467 |
rs141633804 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92358152 | GAGGCTGAGGCAGGA[G/T]AATCACTTGAACCGA | 54467 |
rs141692122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92297493 | TTATTTCTCACCGCT[A/G]TAATCCTTAATATCT | 54467 |
rs141698304 | snp | C/G | 0.0026867 | 0.0365531 | missense, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92398691 | CCAGCTCCCCTGTAT[C/G]AAAGATGGGTCAGAA | 54467 |
rs141709657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92357886 | TTGTTATTACTATAC[G/T]TTGGAGAATTCTGAG | 54467 |
rs141730298 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305615 | TGGTGGGGGAGCCTA[G/T]TGTAAAGAGGCTTCT | 54467 |
rs141731946 | snp | C/G/T | 0.000399281 | 0.0141238 | splice-acceptor-variant, upstream-variant-2KB, intron-variant | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245172 | ATGAAAGCCAAAAAC[C/G/T]TTAAAAGGTGGAGAA | 54467 |
rs141740928 | snp | A/G | 0.000165615 | 0.00909836 | synonymous-codon, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92352547 | AGCAGTAAGACTAAC[A/G]AAACAAGGGTCAAAT | 54467 |
rs141750901 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303364 | CAGATTTTGGAGCAT[G/T]TCAGATTTCTGAATT | 54467 |
rs141772438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92253405 | GAACCACAACCCTTC[A/G]CTGGGCCTATGACTC | 54467 |
rs141813467 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92293102 | CTTGGCAGACATCTT[A/T]CTCTGATACTTAGCT | 54467 |
rs141825480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379640 | AAACATGAGTTATTT[A/G]AATGGTATAAGGACT | 54467 |
rs141912597 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92286886 | AATACTATTTAGAAC[A/G]TATCCAGAATCCAGA | 54467 |
rs141927103 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92378245 | ATTTTTTTTTCATTT[A/G]GAATATTTGCAGTAT | 54467 |
rs141931402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92374437 | GAGCTGAGATTGTGC[C/T]ATTGCACTCCAGCGT | 54467 |
rs141949154 | in-del | -/TTGT | 0.118933 | 0.212888 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92373842 | CCCCTAAAAATAAGC[-/TTGT]TTATTTTAAAAACAC | 54467 |
rs141950166 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314246 | GAGGCTACAGTGAGC[C/T]GTGATCATGCTACTG | 54467 |
rs141963697 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319639 | CTAAATATCCTGTCA[C/T]CTTCATAGCCATAAA | 54467 |
rs141965595 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92380840 | TCTAAAAACCAGAGC[A/G]CCCCATCTCCTCCAG | 54467 |
rs141979619 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248711 | AAGTCATTATTAAAG[-/A]AGACCAGTCTGTGGG | 54467 |
rs142066718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379416 | AATTCAGAAGTTATA[C/T]GGCGGGATTAAGGGG | 54467 |
rs142091128 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279354 | CTTCTTGTGATGTGC[A/G]CCAACTTGTAGCTTT | 54467 |
rs142108881 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92325117 | TTAGACCTAGGTTGG[C/G]GTCAGATTCTGTAGG | 54467 |
rs142140877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92377113 | TTGGCTTTTCAACAT[A/G]CCTTCCTTACTAAGC | 54467 |
rs142214324 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92317169 | TTACTATAAGTTCCC[C/T]GTATTGAATAAATTA | 54467 |
rs142259592 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92329663 | CCATTGTATTGATTA[A/G]TGGGCAGCAATATTC | 54467 |
rs142323633 | snp | C/G | 0.00252844 | 0.0354659 | missense, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92398908 | TCAAGTCAAACACCT[C/G]AAACCTCAAGTGACT | 54467 |
rs142343515 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344120 | TAGGCGCAAAAGTGA[C/T]TGCAGCTTTTGCTAT | 54467 |
rs142383512 | snp | A/C | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92253713 | CTTTCCATTCTTTTT[A/C]ACAACTTACATAGTA | 54467 |
rs142454954 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285561 | TATTTTCTAGATGAG[A/G]AATCCTCAGTTGTCA | 54467 |
rs142463996 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92386324 | TTTAAACTACCCCCA[A/C]ATCTTTCCATAATGC | 54467 |
rs142474134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92251669 | TCCTCATTACAGTCT[G/T]TTTCTGAACCTTTTG | 54467 |
rs142476260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92346707 | CTTAATTAGGAAGTA[C/T]TACCTGAGCTCTACC | 54467 |
rs142476650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92349806 | TGGTGAAACTGAGGC[C/T]TAGAGCAGTTAAATA | 54467 |
rs142493982 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400335 | TGTAATTAGGATACA[A/G]TGGTACAGTGTGTAA | 54467 |
rs142503959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303734 | AAATGAAGCAGTTGG[C/T]AATTTAAAGTTTAGA | 54467 |
rs142527380 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258333 | ATCCTTGAGAGAATT[C/G]AGTGTTAATGTCCTA | 54467 |
rs142537892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248321 | GGCTCTAACAGGTAG[A/G]TGACTCCTGAAACAT | 54467 |
rs142542281 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309194 | GTGTAACCTTTACCC[A/G]TTAGTTAGTTAGTGA | 54467 |
rs142572815 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92344659 | TTTTGCAACATGTAA[-/G]TTTGATGTTGGCCCA | 54467 |
rs142577402 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92341429 | ATTTATACCAAGGAA[A/G]TACCAATATAAACAT | 54467 |
rs142579693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255358 | TAAATAAACAAGGGG[A/G]ATTATTTTCCTCAAG | 54467 |
rs142592745 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92324220 | TATTTTATGTTATGA[A/G]TTTTACCTGAATTTT | 54467 |
rs142596740 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284270 | AGGCATGTACTGGGG[A/G]GTCAGGGCACATAAG | 54467 |
rs142677598 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364983 | ACTTACAGAACATAT[A/G]TGTGGAGATGTCCAG | 54467 |
rs142686057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92268312 | CTTAATAGAGAAGTG[A/G]TGGAACCGCTGTCAG | 54467 |
rs142709829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274130 | CAAGAATTTATTTTA[C/T]CTCCCTCCCCTGAAC | 54467 |
rs142759969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279929 | AATTGTCAGCCTCTA[C/T]GGGTCAGAATCTGAT | 54467 |
rs142809981 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340046 | TCCCTTGGCCTTAAA[A/G]AACATTAATTTGTGT | 54467 |
rs142870940 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361317 | ATTTCCCAAATTCCA[A/G]TAAAAGTAAATTGAG | 54467 |
rs142899528 | snp | C/T | 0.0242459 | 0.107401 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92327765 | GCCCATTTAACTTTA[C/T]TTTTTTTCTTTTCAA | 54467 |
rs142922493 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334484 | AAATTATCTTACAAA[G/T]AATTGTTTCCTGATT | 54467 |
rs142938419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275322 | TCTCTGTACTTAGAT[A/T]TTACTGATGTAAGTC | 54467 |
rs142939460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345326 | ACAAATAATTTTTCT[C/T]AGTATTTTAGTTTAT | 54467 |
rs142941479 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92284020 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 54467 |
rs142970005 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92354490 | AGAACCTAACAAAAT[A/C]ATCATTTTTTGGACA | 54467 |
rs142980677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92288484 | ATAGAACACAGTCAA[C/T]TGGCTTTTTACAAAG | 54467 |
rs142989762 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296077 | TTTTCCTGTTTCTTC[C/T]GTGTACAAATTATTG | 54467 |
rs143004406 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92282296 | GTAGCTGGCATTACA[A/G]GCACGTGCCACCATG | 54467 |
rs143007341 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92381024 | AAAAAGATTAGATGA[A/G]TGGCTAACTAGAATA | 54467 |
rs143066017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92364005 | TCCTGTTCATGCACC[A/G]TTTAGTCAACAGATT | 54467 |
rs143086405 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92309285 | AGACAAGATCTCTCT[A/G]TGTTGTCCAGGCTGG | 54467 |
rs143118402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342180 | GTGTGATCATGGGAC[A/G]AACACAGCCTTTGGA | 54467 |
rs143179343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92249391 | CAGGTTTTTAAGCCA[C/T]TTGACCCTGTTGCAA | 54467 |
rs143193761 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92301847 | CTTTCTCACAAGTTG[A/G]TGACTATTACTTTCT | 54467 |
rs143213425 | in-del | -/TA | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92306225 | TGGAGTTCAGAAGAC[-/TA]TAATGGCTCCACTGA | 54467 |
rs143215997 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, utr-variant-5-prime | KRIT1, ANKIB1 | GRCh38.p7 | 7:92246005 | TGCTGCCGTTCCTGC[C/T]CCTTTTCACTGGACC | 54467 |
rs143216635 | in-del | -/TTGAG | 0.0930568 | 0.194599 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338478 | TGTTTTATTAAATGT[-/TTGAG]TTATGTGTATATAAT | 54467 |
rs143262504 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92346075 | TACTCTTCTCTTTCT[G/T]CCTTCCTTTTATCAC | 54467 |
rs143308723 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92366526 | AAGCAGTCTTAAACT[A/G]TGGGTATGATCTTTT | 54467 |
rs143347738 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92371913 | GCTAGTCACCTTCCC[A/C/T]GCTAGTCACCTTCCC | 54467 |
rs143347744 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311514 | GCCTGTTTCTTGACT[A/G]CATCTGTGGAAGTAT | 54467 |
rs143362665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92379090 | AGGTTTTGTTTCGGA[A/G]TCTAAGTAAACTAAT | 54467 |
rs143386540 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92314068 | TTTGGTTGGCCGAGG[C/T]GGGAGCGTATCTTGA | 54467 |
rs143420616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92332340 | CTGAACCATTAGGAA[A/G]ATTTATAGATTGTAT | 54467 |
rs143487638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92313773 | CCTTCACATTCTGAA[C/T]GTTTATCTCTGGGAA | 54467 |
rs143540342 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367876 | AAATTCAGTCTTTGA[C/G]TAGGTGCAGTGGTTT | 54467 |
rs143560940 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269617 | TATAGACTAGAATTA[G/T]TCTGACTTTATTCTA | 54467 |
rs143602815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275979 | TCATAACCTTATATA[C/T]ACATACACATGCCAT | 54467 |
rs143610417 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92352036 | CCCCTCTTTAACATA[G/T]AAAGTATAATATTGA | 54467 |
rs143684925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375877 | GAAAGTCAAAATGAC[C/T]GCTTAATCCATAGGC | 54467 |
rs143717542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92343350 | AATTGAATCCTATCC[C/G]TTTCTTGAAAGGTTC | 54467 |
rs143724079 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92388931 | GGCAATATCAAACTC[C/T]TGAAGTATTGTCCAC | 54467 |
rs143738412 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92286276 | CTCACCATCAGGGAA[A/G]TCTACTGTAGAGGGA | 54467 |
rs143761292 | snp | A/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335755 | CTGTTTAGTCCATTT[A/G]CATTTAATGTAATAT | 54467 |
rs143798332 | snp | C/T | 0.046775 | 0.145601 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92339331 | ACAGGCGTGAGCCAC[C/T]GCACCTGGCCAAAAA | 54467 |
rs143848097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92245499 | AGTCGAACTTGCTCC[A/T]CCTGTTTCCCGAAGG | 54467 |
rs143899568 | in-del | -/GT | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290529 | CTAAATTGAGTATGA[-/GT]GTGTGTGTGTGTGAC | 54467 |
rs143954883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92345690 | ATTGCTATAATGAGC[A/G]CTGTAATGTCATGTT | 54467 |
rs143955496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92389464 | CCCCTTCTTTCTTTG[A/G]ATTTTTTATTAACTA | 54467 |
rs143974532 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92290285 | CCTGTTTCTCTACTG[C/G]CTAAAGCATTTAGTT | 54467 |
rs143993789 | snp | A/C | | | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294544 | CATAATTTATACAGA[A/C]ATTTAAGTGTTTTCA | 54467 |
rs144036711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92394699 | TCTGTTGAGCCTTGA[C/T]GACACTTAAGTCATC | 54467 |
rs144083298 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92289381 | TATCCTTTTGTTCAT[G/T]TGTATTTTTTGACTG | 54467 |
rs144084878 | in-del | -/T | 0.336702 | 0.234484 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92347275 | TATGAGTTTTTTTTT[-/T]GTTTTGTTTTTTGTT | 54467 |
rs144102934 | in-del | -/TTC | 0.260504 | 0.249779 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92319607 | AACTCAGTTTGTGTG[-/TTC]TTCTTTACAGTATTC | 54467 |
rs144147952 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92368461 | GTGACTCATGCCTGT[A/G]ATCCCAGTACTTGGA | 54467 |
rs144166329 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92376459 | TATTTTTTATTTTTT[A/T]TTTTTTTGAGACAAA | 54467 |
rs144186743 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315866 | AATGTGAAGGCCAAG[A/G]AAGATAGAAAATTTT | 54467 |
rs144206155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92321918 | CTGGCCCTTCACATG[A/G]TTATTTAATCCACAT | 54467 |
rs144206852 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283933 | GTGCCACCAGGCACA[A/G]CTAATATTTGTATTT | 54467 |
rs144259429 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92384124 | AAATCATGAGTGAAC[G/T]CCCATTCACAATTGC | 54467 |
rs144268665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92367250 | GAGAAAGTCCCAGTT[A/G]TTGTTAAGAAAAGCC | 54467 |
rs144341156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269060 | ATGTTTGACTTTAAA[C/G]AGGAAGAACATTAGA | 54467 |
rs144378428 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92320848 | ATTTAATGATTTTTC[A/G]TTGTACTTAGAATAA | 54467 |
rs144380190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92277365 | AGTTTTTTGACTTGG[A/T]TTACAGGGGTATTAA | 54467 |
rs144380209 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335854 | TTCTCTGTTCCTCCT[C/T]CTCTGCTGTATTTTG | 54467 |
rs144397620 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92401464 | AATTAAATCCCTCCA[A/G]TGTGATGGGATCAAT | 54467 |
rs144401696 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92304988 | TATTCTTATATTTCC[A/C]CTTAGTTATAACACT | 54467 |
rs144419563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92280616 | CTCTTTCTCCTCCTA[C/T]CTCAGGAAAGAACAA | 54467 |
rs144484895 | snp | A/G | 0.00140816 | 0.0264971 | missense, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92390016 | TTGAAGATGCAGTTC[A/G]TGTGCTCTTAAAAAC | 54467 |
rs144497538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92394350 | CTAAACCCTTTTCAT[A/G]TACATTCTTGAAGAT | 54467 |
rs144505835 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92262317 | ACTTGAATGTCAACA[C/T]GCATAGTAATAGGGG | 54467 |
rs144568365 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92340521 | CATTGGAATACCAAG[A/G]AAAAAAAAGGATGAG | 54467 |
rs144686785 | in-del | -/T | 0.0452528 | 0.143452 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92269529 | TATTTAAGTATGTGA[-/T]TTTTTTAAGAAAGCT | 54467 |
rs144701105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92335518 | TTGTATATAGCTCCT[C/T]CTTAATGGTGTCAAT | 54467 |
rs144721889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279426 | CAGAAATATAGAGTC[A/G]ATCAGCAGCTCAATT | 54467 |
rs144754235 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355208 | AATTATCTCAAGACA[A/G]TATTCAAAACTTAGA | 54467 |
rs144792934 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296268 | TGCTCTGTCACTCAG[A/G]CTGGAGTGTAGTGGT | 54467 |
rs144793182 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92360631 | ATATGGTAATTCTAA[A/G]TTTAACTTTATGAGG | 54467 |
rs144829806 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305014 | ACACTCGTGGATAGA[C/T]TTTAAATGACTATAA | 54467 |
rs144833260 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92372561 | ACCTTCAATTAAATA[A/C]GTAACTGTTTATTAT | 54467 |
rs144837233 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92274947 | AAATATTTTTCAGTC[C/T]CTGCAGTTTTTAGCC | 54467 |
rs144882766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92260669 | GCATGAGTCACAAAG[C/T]GAGACCCTGTCTCAA | 54467 |
rs144899471 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92361491 | GGCCTGTTCTTCTGC[A/G]TGTCTAAAAAGCTGC | 54467 |
rs144917463 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92336852 | TTGGTTGCTCTCTAG[C/T]GTCCTCAGATAGTTG | 54467 |
rs144919881 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92266484 | GCCCCCCTCTACCAT[C/T]CCTGGACTGAGATTC | 54467 |
rs144937938 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92281511 | AAAGTAGAATGTCCT[C/G]AGACAAATGGGGCTG | 54467 |
rs145053059 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92376890 | CTAGGGCCTTGCTCT[A/G]GATTAGGATTTGGCT | 54467 |
rs145067084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92334760 | TTTTAAAAATTAATG[C/T]ATGATATAAAGCTTT | 54467 |
rs145076245 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92276802 | CCTGATAATCAGGGT[A/G]CACATGAAAGGAGTG | 54467 |
rs145088450 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92338081 | GAAATAGAAGGAGAA[C/T]GATAAGTCAAAGAAA | 54467 |
rs145161916 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92283162 | AAACTGCCATAGATA[C/T]TTTTATTACTGTCAT | 54467 |
rs145181449 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92285126 | AGGCTGGAGTGCAGT[A/G]GCACTATCTCGGCTC | 54467 |
rs145189675 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92356962 | AGATTTCTACTTAAT[A/T]CACTCAGAATTGCTT | 54467 |
rs145190373 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92385197 | ACCATCTCACACCAG[G/T]TAGAATGGCGATCAT | 54467 |
rs145220991 | in-del | -/ATAAAAGAGATC | 0.0941369 | 0.195465 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258845 | TAAATAAAAGAGATC[-/ATAAAAGAGATC]TCTCCATTTGGAATT | 54467 |
rs145249990 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312034 | TGCTACCATTATCTC[C/T]TTATCCAGTATTGAT | 54467 |
rs145291912 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92330331 | GTTAGGTATTGTTTC[C/T]ATAATACCTAATATA | 54467 |
rs145377740 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92291189 | GTTCCAGCTACTCGG[G/T]AGTCTGAGGCATGAG | 54467 |
rs145407418 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92362607 | TGTACTTTGTGGAAG[C/T]AGTATATGATCTGTA | 54467 |
rs145457631 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92296078 | TTTCCTGTTTCTTCC[A/G]TGTACAAATTATTGT | 54467 |
rs145480856 | in-del | -/CTC | 0.0236746 | 0.106192 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92320060 | TATGAATCCCATTTA[-/CTC]CTCCTACTACAAGAC | 54467 |
rs145487340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92305871 | GAGAGATTTACTGCC[C/T]GTGAGATATGTATTT | 54467 |
rs145516049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92253551 | GCAGACACCTTTACA[C/T]ATTCTAATAGTTAAT | 54467 |
rs145526214 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92311998 | TAGTGCTTGATTCTT[G/T]ACTCTAGATTCTATT | 54467 |
rs145556903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92258073 | TAGGATATGATATTC[C/T]GATTTGAAAAACATT | 54467 |
rs145558295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308777 | CAGCTACCAACATTC[A/G]TATCCATCCTTACAT | 54467 |
rs145595538 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92312600 | TCATGAAATAATTCT[A/G]TTTATTCTTTTCAAT | 54467 |
rs145600080 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92323564 | AGATTTTTTCAACCC[A/G]TATTGGATTTGTTTT | 54467 |
rs145635930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92308678 | ATTAGATAAAATCAC[A/G]CATATAATATGAGAT | 54467 |
rs145704167 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92263107 | AATCTGTGATTTCTT[A/T]TTGTAAAATGTAGGC | 54467 |
rs145715174 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92383736 | GGTATTGATGGAACA[A/G]ATCTCAAAATAATAA | 54467 |
rs145726501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92320343 | ATGGAACTGCCCCCC[A/G]TCATGGAGTGACATG | 54467 |
rs145752626 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92315099 | ATTTGTGTACATTCT[C/G]TATACCTGCTATCAC | 54467 |
rs145770072 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264243 | GCAGAGGGAAAACCT[A/G]AGTTACATGTTTAAA | 54467 |
rs145828789 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92342664 | CAGTTAAAAAATTAT[A/G]TATACTTTTGGAAAG | 54467 |
rs145839958 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | KRIT1, ANKIB1 | GRCh38.p7 | 7:92244550 | GTACTTGACTACTTA[A/C]AATCTACATTCTTCC | 54467 |
rs145870093 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92325477 | AAAAACTTTCCTGGC[G/T]ATTTTTTCCACCCTC | 54467 |
rs145893520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92333387 | CAAGGGTGTTACCCT[C/G]CCTCCTGCCACAGGC | 54467 |
rs145904928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92337441 | TACTTTTTCCAGATC[G/T]TTTTTAAAAATGATA | 54467 |
rs145936592 | snp | G/T | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92264185 | TTTGTTTGTTTGTTG[G/T]TTTTTTTTTTTCTGG | 54467 |
rs145950740 | in-del | -/G | | | intron-variant | ANKIB1 | GRCh38.p7 | 7:92375259 | GAGTTGGCTGTGGCA[-/G]GTTTCTTAAAATAAG | 54467 |
rs145951541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ANKIB1 | GRCh38.p7 | 7:92294726 | TTGGACAGTGTTAAA[A/G]ATTTGAGATTTTTTT | 54467 |
rs145953410 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92395175 | TACCCAGGTAATAGC[G/T]ATGGTCCCAGGTTGT | 54467 |
rs145959355 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | ANKIB1 | GRCh38.p7 | 7:92400381 | ACTGTTGGAATGGCT[A/G]TTTTACTTAAATATT | 54467 |
rs145962081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92303877 | GAATGTAGAAGAAAT[A/T]GAGGTAACAGCTATA | 54467 |
rs145976295 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92248697 | ATTTGGGAGTGGACT[A/G]AGTCATTATTAAAGA | 54467 |
rs145988524 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92255480 | CAGGCTTGTCACCTC[A/C/G]TGGTCTTCAGATGGC | 54467 |
rs146030142 | in-del | -/T | 0.0923359 | 0.194016 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92355358 | ACAACTCTTCACAGA[-/T]TTGTTGTCAGAAATA | 54467 |
rs146073524 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92322545 | TCATCCTGACTGTAT[A/C]CCCGAGTGGTAACAG | 54467 |
rs146087806 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92328179 | TAATTTTAGAAATAT[A/G]TCTAATTTGAGTGAG | 54467 |
rs146099012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92275510 | TATTTAATTGGCAGA[A/G]GTCAGGGATGATTAA | 54467 |
rs146110222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ANKIB1 | GRCh38.p7 | 7:92279099 | CATACAGCCTAGATC[C/T]TTTGTGTGTGCAGTT | 54467 |