SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1054618 | snp | C/T | 0 | 0 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521333 | CCCCTGGGCCCTGGT[C/T]TTCCTCCAACATCAC | 4542 |
rs1054619 | snp | C/T | 0 | 0 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521303 | CACCTGCTGCCCATT[C/T]TCCATTTCTGTGTGT | 4542 |
rs1054621 | snp | C/T | 0 | 0 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521263 | GACTAACAGCAGAAT[C/T]TACCTCCCAACTGCC | 4542 |
rs1054622 | snp | A/G | 0 | 0 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521237 | CTGCCATGTGATTAA[A/G]AAATGGGTCTTGAGT | 4542 |
rs1054623 | snp | G/T | 0.340559 | 0.233022 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521202 | TGCTGTTGGCAAAGT[G/T]CCAGGCACAGTTGGG | 4542 |
rs1975029 | snp | A/G | 0.460477 | 0.134905 | intron-variant | MYO1F | GRCh38.p7 | 19:8537723 | CACCCagccaggtat[A/G]gtggctcatgcctgt | 4542 |
rs2013694 | snp | A/G | 0.16618 | 0.23553 | intron-variant | MYO1F | GRCh38.p7 | 19:8551508 | AAAAATTAGCCAGAT[A/G]TGGTGGCGTGTGACT | 4542 |
rs2013882 | snp | C/T | 0.488965 | 0.0734569 | intron-variant | MYO1F | GRCh38.p7 | 19:8551036 | CAGGCGTGAGCGTCG[C/T]GTCCGGACTGGGCTT | 4542 |
rs2288411 | snp | C/T | 0.000367124 | 0.0135435 | missense | MYO1F | GRCh38.p7 | 19:8522805 | GCAATGGGGTGCCCC[C/T]CTCTGCCAGAGGGGG | 4542 |
rs2303686 | snp | A/G | 0.271231 | 0.249107 | intron-variant | MYO1F | GRCh38.p7 | 19:8550384 | CCAACCAACTGTCCC[A/G]TTTTTGCCCTGACCT | 4542 |
rs2303687 | snp | C/G | 0.464523 | 0.128375 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526688 | GCTTCGGCCCCGGCC[C/G]CGGCCCCGCCCCTGC | 4542 |
rs2340539 | snp | C/G | 0.404209 | 0.196773 | intron-variant | MYO1F | GRCh38.p7 | 19:8527159 | GGTGCAGGACGGAAG[C/G]ATTTGGCATCTAAGG | 4542 |
rs2913922 | snp | C/T | 0.342358 | 0.232314 | utr-variant-3-prime, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520871 | CTCACGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 4542 |
rs2913923 | snp | A/G | 0.460589 | 0.13473 | intron-variant | MYO1F | GRCh38.p7 | 19:8538689 | acctcctgggctcaa[A/G]tgatcctcctgcctc | 4542 |
rs2913925 | snp | A/G | 0.244786 | 0.249946 | intron-variant | MYO1F | GRCh38.p7 | 19:8554577 | CATACTGGGCCTGGC[A/G]GGGGAGGTCAGGTCT | 4542 |
rs2913926 | snp | A/G | 0.22263 | 0.248497 | intron-variant | MYO1F | GRCh38.p7 | 19:8555042 | TACAAAAAATTACCC[A/G]GGCATGGTGGTGCAT | 4542 |
rs2913930 | snp | C/T | | | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520572 | tgctaggattacagg[C/T]gtgaggcaccgcgcc | 4542 |
rs2967589 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8525178 | gcaccccagcctggg[A/C]gacagagttggactc | 4542 |
rs2967590 | snp | C/G | 0.426831 | 0.264938 | intron-variant | MYO1F | GRCh38.p7 | 19:8528838 | TGAGAGGAAGTGAGC[C/G]GGTGTGTATCTGAAC | 4542 |
rs2967591 | snp | C/T | 0.468349 | 0.121752 | intron-variant | MYO1F | GRCh38.p7 | 19:8532744 | TAAGCAAAAATTAGC[C/T]GAGGGTGATGGCACG | 4542 |
rs2967592 | snp | C/T | 0.369346 | 0.219673 | intron-variant | MYO1F | GRCh38.p7 | 19:8533396 | gtcttgctctgtcgc[C/T]caggctggagtgcag | 4542 |
rs2967593 | snp | C/T | 0.210605 | 0.246877 | intron-variant | MYO1F | GRCh38.p7 | 19:8533417 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 4542 |
rs2967594 | snp | C/T | 0.204803 | 0.245881 | intron-variant | MYO1F | GRCh38.p7 | 19:8535589 | GCTAGTTTTATTTTG[C/T]CTTTTTTCTGTTCTA | 4542 |
rs2967766 | snp | C/T | 0.444444 | 0.157135 | intron-variant | MYO1F | GRCh38.p7 | 19:8548602 | ATTTTCTTTTTTTTT[C/T]TTTCTTTTTTTTTTT | 4542 |
rs2967767 | snp | A/G | 0.178785 | 0.239642 | intron-variant | MYO1F | GRCh38.p7 | 19:8542757 | AAAAATCAGCCAGGT[A/G]TGGTGGCACACGCCT | 4542 |
rs2967768 | snp | A/T | 0.485664 | 0.0834419 | intron-variant | MYO1F | GRCh38.p7 | 19:8553894 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 4542 |
rs2967769 | snp | A/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8553896 | cacacacacacacac[A/T]ctctctctctctctc | 4542 |
rs2967770 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8541427 | AAAAAAAAAAAAAAA[A/C]ACACACACACACACA | 4542 |
rs2967771 | snp | A/G | 0.460589 | 0.13473 | intron-variant | MYO1F | GRCh38.p7 | 19:8539011 | ggcgtgagccactgt[A/G]cccagcctatctaat | 4542 |
rs2967772 | snp | C/G | 0.191461 | 0.24305 | intron-variant | MYO1F | GRCh38.p7 | 19:8538225 | TAATCCCAGGACTTT[C/G]GGAGGCTGAGGCAGG | 4542 |
rs2967773 | snp | A/T | 0.222333 | 0.248464 | intron-variant | MYO1F | GRCh38.p7 | 19:8533193 | TCTCTACCAAAAAAA[A/T]ATATATATAATAATA | 4542 |
rs2967774 | snp | C/T | 0.363678 | 0.22266 | intron-variant | MYO1F | GRCh38.p7 | 19:8527323 | GGTGAAGCCAGGTCC[C/T]TACCTGCCGCACAGT | 4542 |
rs2967775 | snp | C/T | 0.301177 | 0.244706 | intron-variant | MYO1F | GRCh38.p7 | 19:8521913 | TCCTGCCTCAGCCAC[C/T]GAAAGTGCTGGGATT | 4542 |
rs2967776 | snp | A/G | 0.303938 | 0.244112 | intron-variant | MYO1F | GRCh38.p7 | 19:8545429 | CTGGGGTTCCCGGGG[A/G]AATGTTTATTGAATG | 4542 |
rs2967777 | snp | G/T | 0.466824 | 0.124448 | intron-variant | MYO1F | GRCh38.p7 | 19:8545511 | GGACATTTTGGTTGT[G/T]ATCTGTCGCTGGAAG | 4542 |
rs2967778 | snp | A/C | 0.466308 | 0.125343 | intron-variant | MYO1F | GRCh38.p7 | 19:8545512 | GACATTTTGGTTGTT[A/C]TCTGTCGCTGGAAGT | 4542 |
rs3097181 | snp | C/G | 0.293807 | 0.246132 | intron-variant | MYO1F | GRCh38.p7 | 19:8544812 | ACGGAGTCTTGCTCT[C/G]TTGCCCAGGCTGGAG | 4542 |
rs3111576 | snp | A/G | 0.162253 | 0.234095 | intron-variant | MYO1F | GRCh38.p7 | 19:8546010 | TGCTGTGGACAACCG[A/G]AATGCAACTGCACTG | 4542 |
rs3213834 | snp | C/G/T | 0.0108079 | 0.0727137 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8530370 | TCCACCCTCTGTCCC[C/G/T]GCAGCTTCCAACATC | 4542 |
rs3764550 | snp | A/G | 0.219049 | 0.248077 | intron-variant | MYO1F | GRCh38.p7 | 19:8544628 | CCTGACCCCTGCAAC[A/G]CCTTTTGTGCTTGTA | 4542 |
rs3815907 | snp | A/G | 0.21695 | 0.247806 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8530009 | AGCCTAGATCCATCT[A/G]TTCCATCACAGGTAT | 4542 |
rs4040643 | in-del | -/TT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8541445 | ttttttttttttttt[-/TT]ngagacagaatctcc | 4542 |
rs4072910 | snp | C/G | 0.466618 | 0.124806 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8579147 | acctggccatgctaa[C/G]cgctcaagcaaaggc | 4542 |
rs4488592 | snp | A/G | 0.306679 | 0.24349 | intron-variant | MYO1F | GRCh38.p7 | 19:8575568 | TCTAACAGACAGACC[A/G]TGGCCCGATAGCAGT | 4542 |
rs4542783 | snp | C/T | 0.498521 | 0.0271552 | intron-variant | MYO1F | GRCh38.p7 | 19:8577276 | TGTCCCTCCTCTTTC[C/T]TCTTCCAGATCCCAC | 4542 |
rs4566305 | snp | A/G | 0.424037 | 0.179474 | intron-variant | MYO1F | GRCh38.p7 | 19:8561147 | ccttggccttccaaa[A/G]tgctgggattacagg | 4542 |
rs4605306 | snp | C/T | 0.496714 | 0.0404017 | intron-variant | MYO1F | GRCh38.p7 | 19:8560807 | gcagtggcacgatct[C/T]ggctcactgcaagct | 4542 |
rs4804310 | snp | C/T | 0.151001 | 0.229563 | intron-variant | MYO1F | GRCh38.p7 | 19:8532981 | GAAAAATTAGCACTT[C/T]ACCCAGAGTGCTTTC | 4542 |
rs4804311 | snp | A/G | 0.125018 | 0.216517 | intron-variant | MYO1F | GRCh38.p7 | 19:8550705 | GCACTCTGTGGTACA[A/G]CGGGGGCAGAAACTG | 4542 |
rs4804312 | snp | C/T | 0.480931 | 0.0957637 | intron-variant | MYO1F | GRCh38.p7 | 19:8575223 | ctaggatgacaggca[C/T]gtgccaccacaccca | 4542 |
rs4804313 | snp | C/T | 0.396727 | 0.202413 | intron-variant | MYO1F | GRCh38.p7 | 19:8575502 | ggtggagctcgggct[C/T]gcttgcctgccactc | 4542 |
rs4804314 | snp | C/T | 0.49928 | 0.018956 | intron-variant | MYO1F | GRCh38.p7 | 19:8575632 | AGGACTTCAGAAATA[C/T]TGTTTCATTGAATCC | 4542 |
rs5827003 | in-del | -/A | 0.49753 | 0.0350569 | intron-variant | MYO1F | GRCh38.p7 | 19:8560494 | AGGAAAAAAAAAAAA[-/A]GAACAGGTTCTTGCC | 4542 |
rs7245972 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8553931 | tctctctcgctctct[C/T]tctctctctctgctc | 4542 |
rs7246812 | snp | C/T | 0.375 | 0.216506 | intron-variant | MYO1F | GRCh38.p7 | 19:8571423 | tctctctctctctct[C/T]ttttttttttagatg | 4542 |
rs7247517 | snp | G/T | 0.140242 | 0.224618 | intron-variant | MYO1F | GRCh38.p7 | 19:8537207 | GGCCAGATGTCCCTG[G/T]TCTGTGTGCACCTCC | 4542 |
rs7248239 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | MYO1F | GRCh38.p7 | 19:8567191 | tctgcctcatcctct[C/T]gagtagctgggatta | 4542 |
rs7249449 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | MYO1F | GRCh38.p7 | 19:8537681 | tcaggtgatccatcc[A/G]cctctggctcccaag | 4542 |
rs7249568 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | MYO1F | GRCh38.p7 | 19:8537726 | ggcatgagccactat[A/G]cctggctGGGTGAtt | 4542 |
rs7251254 | snp | A/G | 0.31503 | 0.241394 | intron-variant | MYO1F | GRCh38.p7 | 19:8552222 | TGCAGGTGGGGGAAG[A/G]GTTGGGGATGGGTCT | 4542 |
rs7251782 | snp | A/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543156 | tgatccacccgcctc[A/G]gcctcccaaagtgct | 4542 |
rs7251784 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | MYO1F | GRCh38.p7 | 19:8552642 | atggatattaacatc[A/G]tcaccattttatgga | 4542 |
rs7252717 | snp | C/T | 0.093417 | 0.194889 | intron-variant | MYO1F | GRCh38.p7 | 19:8552700 | tgcatagattttttt[C/T]ccccccaggctacac | 4542 |
rs7252938 | snp | C/G | 0.0670745 | 0.170406 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577668 | AGCTGGCTGCAGGAC[C/G]AACCACCTCTTTTCA | 4542 |
rs7254422 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | MYO1F | GRCh38.p7 | 19:8565530 | ctgggcaacaagtgc[A/G]aaactctgtctcgaa | 4542 |
rs7255459 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MYO1F | GRCh38.p7 | 19:8565293 | cacgcctgtaatccc[A/G]gcactttgggaggtt | 4542 |
rs7256051 | snp | A/C | 0.0333695 | 0.124785 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536005 | tttcttaatctctcg[A/C]tcagtctctctcagt | 4542 |
rs7256500 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | MYO1F | GRCh38.p7 | 19:8569554 | CTACTGTGCATGGAG[A/G]TAGGTGGAGACCAGG | 4542 |
rs7256582 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8553924 | ctctctctctctctc[G/T]ctctctttctctctc | 4542 |
rs7258504 | snp | C/T | 0.349452 | 0.229367 | intron-variant | MYO1F | GRCh38.p7 | 19:8548790 | tatttttagtagaga[C/T]ggggtttcactgtgg | 4542 |
rs7258614 | snp | C/T | 0.338296 | 0.233889 | intron-variant | MYO1F | GRCh38.p7 | 19:8548855 | ggcctcccaaagtgc[C/T]gggattacaggtgtg | 4542 |
rs7258802 | snp | C/T | 0.120674 | 0.21395 | intron-variant | MYO1F | GRCh38.p7 | 19:8571848 | atgatctgcccgcct[C/T]ggcctcccaaagtgc | 4542 |
rs8104131 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8555414 | aaaaaaaaGAACAAA[C/G]AGGGTTGGATCCGGA | 4542 |
rs8104707 | snp | A/G | 0.372995 | 0.217652 | intron-variant | MYO1F | GRCh38.p7 | 19:8547069 | ttggcaggccaaggc[A/G]ggaggattgcttgag | 4542 |
rs8106859 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | MYO1F | GRCh38.p7 | 19:8552805 | CACCCACACAAAGAA[C/T]GAGTCCCAGAACTAT | 4542 |
rs8109435 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559350 | GTGGGGGGTGGGGGG[G/T]GGGGGTGGAGGTGCA | 4542 |
rs8110924 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MYO1F | GRCh38.p7 | 19:8569290 | GACCACAAGCTGAAT[A/G]TGACTCAACCTGCTG | 4542 |
rs9749382 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | MYO1F | GRCh38.p7 | 19:8568354 | cgtgaacctgggagg[C/T]ggagcttgcagtgag | 4542 |
rs10401267 | snp | C/T | 0.00412542 | 0.0452293 | intron-variant | MYO1F | GRCh38.p7 | 19:8541891 | CCGGAGGTCCCCATG[C/T]CTGGGACCACTCACT | 4542 |
rs10401387 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8557286 | tctcaaaaaaaacaa[A/C]caaccaaacaaacaa | 4542 |
rs10402716 | snp | G/T | 0.198944 | 0.244731 | intron-variant | MYO1F | GRCh38.p7 | 19:8525286 | AGTGGTTAGCTGGGT[G/T]TGGGTTTTGAAGGGC | 4542 |
rs10403664 | snp | C/T | 0.200182 | 0.244986 | intron-variant | MYO1F | GRCh38.p7 | 19:8560570 | TGAGAAGGAtttttt[C/T]gttttgttttggttt | 4542 |
rs10405687 | snp | A/G | 0.219648 | 0.248151 | intron-variant | MYO1F | GRCh38.p7 | 19:8545976 | TCGCTTCTCCGCTCT[A/G]TGAAGCCTCCTCGAG | 4542 |
rs10406181 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | MYO1F | GRCh38.p7 | 19:8540555 | tctctactaaaaata[C/T]aaaaattagcggggc | 4542 |
rs10406855 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | MYO1F | GRCh38.p7 | 19:8563408 | attcaagcgattctc[A/G]tgcctcagcctcctg | 4542 |
rs10407838 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | MYO1F | GRCh38.p7 | 19:8571027 | CCATCAATGGTGGCC[A/G]TGAGCTGGCCAGGAG | 4542 |
rs10408143 | snp | C/T | 0.498253 | 0.0295011 | intron-variant | MYO1F | GRCh38.p7 | 19:8522898 | GAGGAGGACTTGGCT[C/T]CAAGTTCTCAGGCTG | 4542 |
rs10408572 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8523235 | agacggagtttcatc[A/G]tgttagccaggatgg | 4542 |
rs10409059 | snp | C/T | 0.314544 | 0.241524 | intron-variant | MYO1F | GRCh38.p7 | 19:8551496 | AGCTGGGATTACAGT[C/T]ACACGCCACCACATC | 4542 |
rs10409154 | snp | C/G | 0.383824 | 0.211166 | intron-variant | MYO1F | GRCh38.p7 | 19:8546225 | atgtgccaccacgcc[C/G]gactaattttgtatt | 4542 |
rs10409874 | snp | A/G | 0.332337 | 0.236052 | intron-variant | MYO1F | GRCh38.p7 | 19:8551499 | TGGGATTACAGTCAC[A/G]CGCCACCACATCTGG | 4542 |
rs10411722 | snp | C/G/T | 0.0549768 | 0.157587 | intron-variant | MYO1F | GRCh38.p7 | 19:8540193 | GGttttttggtttgt[C/G/T]ttttgaggcagggcc | 4542 |
rs10414158 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | MYO1F | GRCh38.p7 | 19:8523233 | agagacggagtttca[C/T]catgttagccaggat | 4542 |
rs10415142 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8568303 | tggcgggcgcccgta[A/G]tcccagctcctcggg | 4542 |
rs10416039 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | MYO1F | GRCh38.p7 | 19:8568650 | GATTTggccgcgcat[A/G]gtggctcacgcctgt | 4542 |
rs10416597 | snp | C/T | 0.493386 | 0.0571263 | intron-variant | MYO1F | GRCh38.p7 | 19:8567703 | CACAGAGAGGTTAAG[C/T]GTCCTCTTCAAGGAC | 4542 |
rs10417009 | snp | A/G | 0.320814 | 0.239761 | intron-variant | MYO1F | GRCh38.p7 | 19:8547475 | tgggcatggtggtgg[A/G]tgcctgtagtcccag | 4542 |
rs10417466 | snp | A/G | 0.217851 | 0.247924 | intron-variant | MYO1F | GRCh38.p7 | 19:8524928 | GAggccaggcgccgt[A/G]gctcatgcttgttaa | 4542 |
rs10422512 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574581 | TCTTTCTTTCTTTCT[C/T]TCTCTCTCTCTCTCT | 4542 |
rs10422681 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MYO1F | GRCh38.p7 | 19:8526035 | GGCCTTTGTTTAAAA[A/G]TCTGTCTCTCTggcc | 4542 |
rs10422709 | snp | C/T | 0.343477 | 0.231866 | intron-variant | MYO1F | GRCh38.p7 | 19:8560222 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4542 |
rs10422786 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8560316 | ggtgaaaccccatct[C/T]tactaaaaatacaaa | 4542 |
rs10424530 | snp | C/T | 0.493703 | 0.0557558 | intron-variant | MYO1F | GRCh38.p7 | 19:8562241 | ctcctgacctcgtta[C/T]ccgcccgccttggcc | 4542 |
rs10424637 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8522141 | cattctcctgcctca[A/G]cctcccgagtagctg | 4542 |
rs10469478 | snp | G/T | 0.0058139 | 0.0536018 | intron-variant | MYO1F | GRCh38.p7 | 19:8536888 | GAGGTGTCTCGGTCA[G/T]TTCTAGGGGTAACTG | 4542 |
rs11259990 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | MYO1F | GRCh38.p7 | 19:8569882 | CTGCTGGCCTCTCAT[C/T]GCTTAGGAGGACAGG | 4542 |
rs11669933 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574577 | tctttctttctttct[C/T]tctctctctctctct | 4542 |
rs11669936 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574599 | TCTCTCTCTCTCTCT[C/T]TCTTTCTTTCTTTCT | 4542 |
rs11670066 | snp | G/T | 0.499958 | 0.00459246 | intron-variant | MYO1F | GRCh38.p7 | 19:8574933 | gctaatttttgtatt[G/T]ttagtagagacaggg | 4542 |
rs11670281 | snp | A/C | 0 | 0 | splice-donor-variant, intron-variant | MYO1F | GRCh38.p7 | 19:8545648 | GTTGACCCAGCCCTC[A/C]CCAGCTTGTTTTCGA | 4542 |
rs11671997 | snp | G/T | 0.444931 | 0.15653 | intron-variant | MYO1F | GRCh38.p7 | 19:8568646 | AGTGGATTTggccgc[G/T]catggtggctcacgc | 4542 |
rs11672367 | snp | C/T | 0.464629 | 0.128197 | intron-variant | MYO1F | GRCh38.p7 | 19:8569059 | TGAGAGGATTTAAGG[C/T]ATCAGTGTTGGACAG | 4542 |
rs11673177 | snp | A/G | 0.447291 | 0.153545 | intron-variant | MYO1F | GRCh38.p7 | 19:8562606 | agtggtgtaatcata[A/G]ctaactgtagccttg | 4542 |
rs11878208 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | MYO1F | GRCh38.p7 | 19:8575292 | acgttggccaggatc[A/G]tttctatctcttgac | 4542 |
rs11879455 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MYO1F | GRCh38.p7 | 19:8552328 | cagtggcgcaatgtc[A/G]gctcactgcaacgtc | 4542 |
rs11880545 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8531724 | GATGTCACGGTTTCT[A/T]ACACTGTTACTCGAC | 4542 |
rs11880567 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8531835 | GTAAATATGAAAATG[C/T]ggccgggtgcagtgg | 4542 |
rs11881450 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8542948 | ttgctctgttgctca[A/G]gctggagtgctgtgg | 4542 |
rs11881473 | snp | A/G | 0.457037 | 0.140127 | intron-variant | MYO1F | GRCh38.p7 | 19:8543065 | CCCACGACCACGCCC[A/G]GCTGATTTTTGTATT | 4542 |
rs11881996 | snp | A/G | 0.00529873 | 0.0511985 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550238 | TGCCTGCTCCACGTT[A/G]AGGGTCACATTGATG | 4542 |
rs11882152 | snp | C/G | 0 | 0 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550293 | CTGTCCATCTTGCGG[C/G]TGGTCAGCTTCTCCT | 4542 |
rs11882389 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8546154 | atcgcaacctccgcc[C/T]cccgagttcaagcga | 4542 |
rs11882393 | snp | G/T | 0.4628 | 0.13121 | intron-variant | MYO1F | GRCh38.p7 | 19:8531737 | CTTACACTGTTACTC[G/T]ACACTATCCACGAGG | 4542 |
rs11882507 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8531596 | CTGGACCTCCCTGTG[C/G]GTCTCTCCCCATGTG | 4542 |
rs12151191 | snp | A/G | 0.426201 | 0.177351 | intron-variant | MYO1F | GRCh38.p7 | 19:8523313 | gctgggattacaggc[A/G]tgagccaccgcgcct | 4542 |
rs12460069 | snp | C/T | 0.153665 | 0.230694 | intron-variant | MYO1F | GRCh38.p7 | 19:8564616 | CTCAACCCTGAAGAG[C/T]GTCTGAGCTCACTGG | 4542 |
rs12460946 | snp | A/G | 0.158302 | 0.232576 | intron-variant | MYO1F | GRCh38.p7 | 19:8571225 | TCCGTAGCTGCTTCT[A/G]GAGCCAGCTCTCAGC | 4542 |
rs12462245 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543696 | gtggtggtggtggtg[C/G]tggtggtggtgctgg | 4542 |
rs12462386 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543768 | gtggtggtggtggtg[C/G]tggtggtgctggtgg | 4542 |
rs12462590 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | MYO1F | GRCh38.p7 | 19:8531573 | AATTTTTATCTTCCT[C/T]CAAATGACTGGACCT | 4542 |
rs12608739 | snp | C/G | 0.491051 | 0.0662916 | intron-variant | MYO1F | GRCh38.p7 | 19:8563704 | tttagtagagatggg[C/G]tttcactatgttggt | 4542 |
rs12611122 | snp | C/T | 0.286564 | 0.247312 | intron-variant | MYO1F | GRCh38.p7 | 19:8574209 | GAGCCATTATCACCA[C/T]GAACCTGCAACAAGA | 4542 |
rs12971599 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543849 | gtggtggtggtggtg[C/G]tggtggtgctggtgg | 4542 |
rs12972649 | snp | C/G | 0.497984 | 0.0316851 | intron-variant | MYO1F | GRCh38.p7 | 19:8573675 | GCCAACATGGCGAAA[C/G]CCCGTCTCCACTAAA | 4542 |
rs12973191 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574610 | ctctttctttctttc[C/T]ttctttctttctttc | 4542 |
rs12973194 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574619 | tctttctttctttct[C/T]tctttctttctttct | 4542 |
rs12973392 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574636 | ctttctttctttctt[C/T]ctttctttcctttct | 4542 |
rs12973441 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8574703 | TTTCTCTTTCTCTCT[C/T]TCTTTCTTTTTCTTT | 4542 |
rs12975214 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561459 | cttcctccctctctc[C/T]ctctctctctctttc | 4542 |
rs12975224 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561466 | cctctctccctctct[C/T]tctctttctttttct | 4542 |
rs12980251 | snp | A/C | 0.254105 | 0.249966 | intron-variant | MYO1F | GRCh38.p7 | 19:8573083 | GGAGGCTGAGGCGGG[A/C]AGATCACGAGGTCAG | 4542 |
rs12980457 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8565921 | tagtgagacccccat[A/C]tctgcaaaaaaaaat | 4542 |
rs12980898 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574609 | tctctttctttcttt[C/T]tttctttctttcttt | 4542 |
rs12981123 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574669 | ctctttcttctttct[C/T]tctttctttctttct | 4542 |
rs12982567 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561426 | ctccctcccttcctt[C/T]ctcctctccctccct | 4542 |
rs12983080 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561633 | tttctttcttctttc[C/T]ttccttctttccttc | 4542 |
rs12983677 | snp | A/G | 0.498253 | 0.0295011 | intron-variant | MYO1F | GRCh38.p7 | 19:8571576 | CCCGCCACCGCGCCC[A/G]GCTAATTTTTTTTTT | 4542 |
rs12984227 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | MYO1F | GRCh38.p7 | 19:8561103 | ctcaggctgatgtct[A/G]taactcctgggctca | 4542 |
rs13345078 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | MYO1F | GRCh38.p7 | 19:8561730 | atctttttttttgtt[C/T]gtttgagatggagtc | 4542 |
rs13346588 | snp | C/G | 0.117886 | 0.21224 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521342 | GAGGAAGACCAGGGC[C/G]CAGGGGCGGGGGCTG | 4542 |
rs17160563 | snp | A/G | 0.156357 | 0.231799 | intron-variant | MYO1F | GRCh38.p7 | 19:8548030 | CCTGACTGCTTGGCC[A/G]CCCACCTGCTCGGCC | 4542 |
rs28432269 | snp | C/T | 0.213635 | 0.247341 | intron-variant | MYO1F | GRCh38.p7 | 19:8543515 | TGAACATAGGCAGTC[C/T]GGTACCCAAGCTGGT | 4542 |
rs28547526 | snp | A/G | 0.291493 | 0.246533 | intron-variant | MYO1F | GRCh38.p7 | 19:8559624 | CAAGCCTGAGTGGTC[A/G]TGAGGATAGACCGAG | 4542 |
rs28566606 | snp | C/G | 0.136506 | 0.222754 | intron-variant | MYO1F | GRCh38.p7 | 19:8558071 | TGCCGTGGCCTTCTC[C/G]TCTGTGTCCCTTCAC | 4542 |
rs28587245 | snp | C/T | 0.281577 | 0.247998 | intron-variant | MYO1F | GRCh38.p7 | 19:8559720 | TTTGGGAGGCCGAGG[C/T]GGGGAGATCATCTAA | 4542 |
rs28699647 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8524536 | GTTGCAGTGAGCCAA[A/G]ATCATGCCACTGCAC | 4542 |
rs34070649 | in-del | -/T | 0.258843 | 0.249844 | intron-variant | MYO1F | GRCh38.p7 | 19:8571581 | ACCGCGCCCAGCTAA[-/T]TTTTTTTTTTGTATT | 4542 |
rs34105946 | in-del | -/T | 0.482459 | 0.0919928 | intron-variant | MYO1F | GRCh38.p7 | 19:8522024 | TGTCAGTCAGGGTTC[-/T]TTTTTTTTTTTTTTT | 4542 |
rs34243582 | in-del | -/AG/G | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8552922 | TAAGAATGTTACACA[-/AG/G]GGGGTGTCATGGCCT | 4542 |
rs34256101 | snp | A/G | 0.0823912 | 0.185492 | intron-variant | MYO1F | GRCh38.p7 | 19:8537075 | GGCAGAAGTGAAGAC[A/G]GGTGGGTGGGGGGCA | 4542 |
rs34261365 | snp | C/T | 0.49931 | 0.0185575 | intron-variant | MYO1F | GRCh38.p7 | 19:8571751 | TACAGGCACCCGCCA[C/T]CACGCCTGGGTAATT | 4542 |
rs34276116 | in-del | -/C | 0.0444908 | 0.142359 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521176 | CACGCTTGTTAAGGA[-/C]CCCCCCCCTCCCCAA | 4542 |
rs34295411 | snp | C/T | 0.0021919 | 0.0330325 | synonymous-codon, intron-variant, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8541950 | CGAGAGGAACCGAGA[C/T]GTTCTCTTCTCCGAC | 4542 |
rs34367204 | snp | C/T | 0.25214 | 0.249991 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578098 | GGTGCCTTCTTCAGC[C/T]GTGTCTGCTCTGGGC | 4542 |
rs34408419 | multinucleotide-polymorphism | CT/GG | | | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550653 | GAGCTGCAGGACCAG[CT/GG]GCTGGATGCTGGGCG | 4542 |
rs34428318 | in-del | -/T | 0.497803 | 0.033074 | intron-variant | MYO1F | GRCh38.p7 | 19:8523036 | AAAATTATTTTTTAC[-/T]TTTTTTTTTTTTTGA | 4542 |
rs34460450 | snp | A/G | 0.159622 | 0.233092 | intron-variant | MYO1F | GRCh38.p7 | 19:8561852 | CTCCCGGGCAGCTGG[A/G]ACTATAGGCGCGCAC | 4542 |
rs34507143 | snp | C/T | 0.00721357 | 0.0596217 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550268 | GGACAGCCGCTGGGG[C/T]GGGCGCAGCGAGTCC | 4542 |
rs34593851 | in-del | -/C | 0.255224 | 0.249945 | intron-variant | MYO1F | GRCh38.p7 | 19:8575730 | TCATTTTTTTCTCTT[-/C]CTATCATCCTCTGCG | 4542 |
rs34644563 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MYO1F | GRCh38.p7 | 19:8576354 | ACACCACCTCTGCCT[C/T]TTGCCCTATGTCCCT | 4542 |
rs34667346 | in-del | -/G/T/TGA | 0.257732 | 0.24988 | intron-variant | MYO1F | GRCh38.p7 | 19:8554418 | CCTCCCTGGGGGTGG[-/G/T/TGA]TGATGTTTCAGCAGG | 4542 |
rs34751170 | in-del | -/ATG | | | intron-variant | MYO1F | GRCh38.p7 | 19:8554423 | CTGGGGGTGGTGATG[-/ATG]TTTCAGCAGGGGCCC | 4542 |
rs34798332 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561705 | TTCCTTCCTTCCTCC[-/T]TTTTTTTCTATCTTT | 4542 |
rs34804868 | in-del | -/A | | | intron-variant | MYO1F | GRCh38.p7 | 19:8563502 | AGGATTTTTCTTTTT[-/A]CTTTCTTTCTTTCTT | 4542 |
rs34808041 | in-del | -/G | | | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520504 | TCCCCATGTTAGCCA[-/G]GGATGGTCTCGATCT | 4542 |
rs34887428 | in-del | -/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534694 | CAGTGGTGCGATCTC[-/G]GGCTCACTGCAACCT | 4542 |
rs34993471 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8533463 | GGGTTCACGCCATTC[G/T]CCTGCCTCAGCCTCC | 4542 |
rs35089564 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577494 | GAGGGGCCGAGGCCA[C/T]GGGGGAGGGAAGCTG | 4542 |
rs35121916 | in-del | -/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574263 | CAATGACACCAACAA[-/C]CCCAGCAATGACCAC | 4542 |
rs35156710 | in-del | -/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559104 | GGCTGGTCTTGAACT[-/G]CCTGAGTTCAAGCGA | 4542 |
rs35275313 | in-del | -/A | 0.434687 | 0.168495 | intron-variant | MYO1F | GRCh38.p7 | 19:8524583 | GAGCGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 4542 |
rs35285307 | in-del | -/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8539443 | ACCAACAAAAAAACA[-/G]AAATTAGCTGGGTGT | 4542 |
rs35449895 | in-del | -/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8549111 | TGCGCCACCACGCCC[-/G]GGCTAATTCTTGTAT | 4542 |
rs35506435 | snp | A/G | 0.00100721 | 0.0224185 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8553175 | GCGCACAGTCTTGGC[A/G]TTGCCGAAGGCCTCG | 4542 |
rs35515901 | in-del | -/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8564530 | TAGGAACTGCCAGGG[-/C]AAGTCAGAGGCAAAA | 4542 |
rs35536931 | in-del | -/TC/TCTC | 0.385157 | 0.239292 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526349 | CACAAAACTCAAAAG[-/TC/TCTC]TCTCTCTCTCTCTCT | 4542 |
rs35618231 | in-del | -/C | 0.0539704 | 0.155153 | intron-variant | MYO1F | GRCh38.p7 | 19:8552700 | TGCATAGATTTTTTT[-/C]CCCCCCAGGCTACAC | 4542 |
rs35639897 | in-del | -/T | | | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520778 | CCACCACACCCGGCT[-/T]TTTTTTTTTTTTCTT | 4542 |
rs35644247 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8563797 | GATTACAGGGGTGAG[C/T]CACCGCGCCTGGCTT | 4542 |
rs35658338 | in-del | -/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8521815 | TCTACTCTTTAAAAG[-/T]TTTTTTTTTGTAAAT | 4542 |
rs35692978 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559987 | TAAAGAATTAACACT[-/T]CAGCGAGCACCTATG | 4542 |
rs35723384 | in-del | -/T | 0.424037 | 0.179474 | intron-variant | MYO1F | GRCh38.p7 | 19:8572269 | TGGGCATTTTTTTTT[-/T]CCCCTCTGAGACAGA | 4542 |
rs35778736 | snp | C/T | 0.0275837 | 0.114153 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8553226 | GCCTCTGCCCCAGCA[C/T]GTCAAAGATATCATC | 4542 |
rs36025540 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | MYO1F | GRCh38.p7 | 19:8523837 | TTTAAAAAGAATTTT[C/T]AGGCTAGGCGCGGTG | 4542 |
rs55705253 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533609 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 4542 |
rs55711162 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8555480 | CCAGGACAGAGGGAG[C/T]AGTGGCAGCCACAGC | 4542 |
rs55764629 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8521824 | AAAAGTTTTTTTTTT[-/T]GTAAATCTTTTGTAG | 4542 |
rs55770417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8527759 | CTGGGACCACAGGTG[C/T]GCACCACCATGCCCA | 4542 |
rs55833513 | in-del | -/A/AAAAAA/AAAAAAA | | | intron-variant | MYO1F | GRCh38.p7 | 19:8568445 | AAAAAAAAAAAAAAA[-/A/AAAAAA/AAAAAAA]TTAATCACAGGCTGT | 4542 |
rs55872402 | snp | A/G | 0.107341 | 0.205301 | intron-variant | MYO1F | GRCh38.p7 | 19:8529053 | CAAAGCAGGTGGGTG[A/G]ATCAGGTGAAGGTAC | 4542 |
rs55872879 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8532251 | ACCTGCACAGCCATC[A/C/T]GTAGCAGGCCCAGAA | 4542 |
rs55920976 | snp | A/C | 5.62308e-05 | 0.0053021 | missense | MYO1F | GRCh38.p7 | 19:8522534 | TTGCCCCACGCTGCG[A/C]TTCCTCTGCATGCTG | 4542 |
rs56008209 | snp | G/T | 0.000796047 | 0.0199346 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8544459 | GCTCATGATGCCTGG[G/T]GGGCTCTGCGGGGCG | 4542 |
rs56029063 | in-del | -/T | 0.375 | 0.216506 | intron-variant | MYO1F | GRCh38.p7 | 19:8522040 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 4542 |
rs56053232 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8527180 | GCATCTAAGGATCAT[A/G]AGCATAGGGGGCAGG | 4542 |
rs56184962 | snp | A/G | 0.49925 | 0.0193545 | intron-variant | MYO1F | GRCh38.p7 | 19:8564444 | TCCCTGGGGTGCGTC[A/G]GGAGATGACAGAATC | 4542 |
rs56328846 | snp | C/G | 0.0304323 | 0.119541 | intron-variant | MYO1F | GRCh38.p7 | 19:8537084 | GAAGACGGGTGGGTG[C/G]GGGGCACAGAGATGG | 4542 |
rs56369630 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MYO1F | GRCh38.p7 | 19:8544542 | TCAGTGCAGAGATTA[A/G]GGGAGGGAGGGGGTG | 4542 |
rs56843156 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543786 | GTGGTGCTGGTGGTG[C/G]TGGTGGTGGTGGTGC | 4542 |
rs56935925 | snp | A/T | 0.181431 | 0.240413 | intron-variant | MYO1F | GRCh38.p7 | 19:8551929 | GGCTCAGCCCCTGTG[A/T]TCCCTCATCTGCCCT | 4542 |
rs56989930 | snp | C/G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543735 | GTGGTGCTGGTGGTG[C/G/T]TGGTGGTGCTGGTGG | 4542 |
rs57114174 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8546183 | GATTCTCCTGCCTCA[C/G]CCTCCCGAGAAGCTG | 4542 |
rs57151843 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533511 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAACTTTT | 4542 |
rs57169847 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533558 | GAGACATAGTTTTGC[C/T]GTGTTAGCCAGGGTG | 4542 |
rs57312139 | in-del | -/TTCTTTCTCT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574573 | TCTTTCTTTCTTTCT[-/TTCTTTCTCT]CTCTCTCTCTCTCTC | 4542 |
rs57316317 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543693 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGC | 4542 |
rs57365490 | in-del | -/AG | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533593 | AATCTCCTGACCTCA[-/AG]TGATCCGCCTGCCTC | 4542 |
rs57563221 | in-del | -/A | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8539595 | TCTCAAAAAAAAAAA[-/A]TTATTGGATATTATT | 4542 |
rs57614495 | in-del | -/TC | 0.43088 | 0.172575 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536167 | CTCTCTCTCTCTCTC[-/TC]AGTCCCTCTCTATAC | 4542 |
rs57666560 | snp | A/G | 0.000329372 | 0.0128288 | intron-variant | MYO1F | GRCh38.p7 | 19:8542039 | CTGAGAAACCTGGCT[A/G]GGAGGGTGGGCGTGG | 4542 |
rs57842422 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8526137 | TTCAAGACCAGCCTG[A/G]CCAAGATGGTGAAAC | 4542 |
rs57976295 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533500 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCT | 4542 |
rs58076701 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543708 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG | 4542 |
rs58145523 | in-del | -/TTTCTTTC | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574638 | TTCTTTCTTTCTTTC[-/TTTCTTTC]CTTTCTTTCTCTTTC | 4542 |
rs58476251 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533531 | GGCTAACTTTTTTGT[A/G]TTTTTTTAGTAGAGA | 4542 |
rs58501729 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8523555 | GGGGTCTCACTATGT[-/T]GCTCAGGCTGGTCTC | 4542 |
rs58587283 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543828 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG | 4542 |
rs58596348 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8572843 | TGGTACTACAGGTCC[A/G]TGCCACCATGCCTGG | 4542 |
rs58620132 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8551369 | TTTTTTTTTTTTTTT[-/T]GAGATGTAGTCTCAC | 4542 |
rs58623850 | in-del | -/TGTC | | | intron-variant | MYO1F | GRCh38.p7 | 19:8555529 | TGCTGTCACTCTGTC[-/TGTC]CTCTGTGTCACCACT | 4542 |
rs58635686 | in-del | -/TT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533537 | CTTTTTTGTATTTTT[-/TT]AGTAGAGACATAGTT | 4542 |
rs58638075 | in-del | -/TTTTTTTTTTTT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8546070 | TCTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGATGGAGTTTCAC | 4542 |
rs58681956 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543714 | GTGGTGGTGCTGGTG[C/G]TGGTGGTGGTGCTGG | 4542 |
rs58706590 | snp | C/T | 0.331874 | 0.236213 | intron-variant | MYO1F | GRCh38.p7 | 19:8549933 | AGCCCTCTGAGTAGC[C/T]AGAACTACACATGCA | 4542 |
rs58722726 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | MYO1F | GRCh38.p7 | 19:8570374 | TGCACCCAGCCACAT[A/T]TTTTTTTTTATTTGA | 4542 |
rs58816360 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533490 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 4542 |
rs59011759 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543789 | GTGCTGGTGGTGCTG[C/G]TGGTGGTGGTGCTGG | 4542 |
rs59034061 | snp | A/C/G | 0.00914312 | 0.0669923 | intron-variant | MYO1F | GRCh38.p7 | 19:8546158 | CAACCTCCGCCTCCC[A/C/G]AGTTCAAGCGATTCT | 4542 |
rs59048744 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543744 | GTGGTGCTGGTGGTG[C/G]TGGTGGTGGTGGTGG | 4542 |
rs59083919 | snp | A/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8572851 | CAGGTCCATGCCACC[A/T]TGCCTGGCTAACTTT | 4542 |
rs59119488 | snp | A/G | 0.21875 | 0.248039 | intron-variant | MYO1F | GRCh38.p7 | 19:8533980 | ACTTGAGGTCAGGAG[A/G]CCAGCCTGGCCAACA | 4542 |
rs59138202 | snp | A/G | 0.353371 | 0.227628 | intron-variant | MYO1F | GRCh38.p7 | 19:8561213 | ATAAACAGCTGGGAG[A/G]AAGGGTGCACCAGTC | 4542 |
rs59243818 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543858 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG | 4542 |
rs59252510 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYO1F | GRCh38.p7 | 19:8558114 | CAGTGCCAGCACCTT[C/T]TTAGGTTGCCATTTT | 4542 |
rs59301382 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | MYO1F | GRCh38.p7 | 19:8555469 | GCTGAGCTTCCCCAG[A/G]ACAGAGGGAGCAGTG | 4542 |
rs59472184 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8568569 | TGGCTTGACAGTTGA[C/G]TGACTGTGTGACTCT | 4542 |
rs59506897 | snp | A/G | 0.332106 | 0.236133 | intron-variant | MYO1F | GRCh38.p7 | 19:8549806 | CACTGCATCTGGCCA[A/G]AAGTTTTTTTTAGAG | 4542 |
rs59718615 | snp | C/G | 0.193743 | 0.243588 | intron-variant | MYO1F | GRCh38.p7 | 19:8548334 | TGCGGTGTGGGTGGG[C/G]ACAGGAAGTCAGTGG | 4542 |
rs59742577 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543741 | CTGGTGGTGCTGGTG[C/G]TGCTGGTGGTGGTGG | 4542 |
rs59757576 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543777 | GTGGTGCTGGTGGTG[C/G]TGGTGGTGCTGGTGG | 4542 |
rs59758659 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8554273 | GAGGTGACATTTAGA[A/G]GGGACAGACAGACAA | 4542 |
rs59776145 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | MYO1F | GRCh38.p7 | 19:8559259 | AAGCAGAAGTGTCCA[C/T]GTGGGCAACTGTAAG | 4542 |
rs59836911 | in-del | -/CT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533522 | ACCATGCCTGGCTAA[-/CT]TTTTTGTATTTTTTT | 4542 |
rs59880313 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543726 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG | 4542 |
rs59943538 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543771 | GTGGTGGTGGTGCTG[C/G]TGGTGCTGGTGGTGC | 4542 |
rs60042889 | in-del | -/CAAAAAA | | | intron-variant | MYO1F | GRCh38.p7 | 19:8568438 | AAAAAAAAAAAAAAA[-/CAAAAAA]AAAAAAATTAATCAC | 4542 |
rs60096210 | in-del | -/A | | | intron-variant | MYO1F | GRCh38.p7 | 19:8532902 | CAGAAAAAAAAAAAA[-/A]TACACACACACACAC | 4542 |
rs60199031 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | MYO1F | GRCh38.p7 | 19:8558140 | ATTTTTTTCATTTCA[C/T]TTCCTCTCTCAGTTT | 4542 |
rs60369992 | in-del | -/A | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559971 | AAAAAAAAAAAAAAA[-/A]GTAAAGAATTAACAC | 4542 |
rs60396924 | snp | A/G | 0.134594 | 0.221769 | intron-variant | MYO1F | GRCh38.p7 | 19:8539927 | CAGGCCCAGCTCCCC[A/G]TTGTACACCCCAGGC | 4542 |
rs60549817 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8533480 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 4542 |
rs60550068 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543732 | GTGGTGGTGCTGGTG[C/G]TGCTGGTGGTGCTGG | 4542 |
rs60597817 | snp | C/T | 0.221439 | 0.248363 | intron-variant | MYO1F | GRCh38.p7 | 19:8540114 | GGGCAGCCTCAATGC[C/T]GCAACGCAAAATATG | 4542 |
rs60619060 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533559 | AGACATAGTTTTGCT[C/G]TGTTAGCCAGGGTGG | 4542 |
rs60648462 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543801 | CTGGTGGTGGTGGTG[C/G]TGGTGGTGCTGGTGG | 4542 |
rs60799506 | in-del | -/CA | | | intron-variant | MYO1F | GRCh38.p7 | 19:8532949 | ACACACACACACACA[-/CA]ATTGGGCTTTATTTA | 4542 |
rs60806727 | in-del | -/A | | | intron-variant | MYO1F | GRCh38.p7 | 19:8525222 | AAAAAAAAAAAAAAA[-/A]GATGTAGTTTACAGG | 4542 |
rs60849120 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8544220 | TTCCAGCCTGGGTGC[G/T]GGAGGGTGGGGGCTA | 4542 |
rs60971689 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8549389 | GATTCTTCCACCTCA[G/T]CCTCCTGAGTAGCCG | 4542 |
rs61021979 | snp | A/G | 0.00118512 | 0.0243137 | intron-variant | MYO1F | GRCh38.p7 | 19:8554777 | TCGTGTGGTGTCCTG[A/G]TAGGTTTTGTCCTCC | 4542 |
rs61036236 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533540 | TTTTGTATTTTTTTA[A/G]TAGAGACATAGTTTT | 4542 |
rs61070658 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8538604 | TTTTTTTTTTTTTTT[-/T]AAGAGACAGGGTCTC | 4542 |
rs61078650 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8542618 | GCTTTTTTTTTTTTT[-/T]GAGAAAGAGTCTTGC | 4542 |
rs61342405 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543705 | GTGGTGGTGGTGGTG[C/G]TGCTGGTGGTGGTGG | 4542 |
rs61370919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8542725 | CCTGTCTCAGCCTCC[C/T]GATGAGCTGGGATTA | 4542 |
rs61400406 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533603 | ACCTCATGATCCGCC[C/T]GCCTCGGCCTCCCAA | 4542 |
rs61430573 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533512 | GGCGCCCGCCACCAT[A/G]CCTGGCTAACTTTTT | 4542 |
rs61463028 | in-del | -/CC | 0.193661 | 0.243569 | intron-variant | MYO1F | GRCh38.p7 | 19:8548333 | TGCGGTGTGGGTGGG[-/CC]GACAGGAAGTCAGTG | 4542 |
rs61744125 | snp | C/T | 0.00503193 | 0.0499063 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8544375 | CACAGCCGCCTGCAG[C/T]TTCTGCAGCAGTGTC | 4542 |
rs62119397 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MYO1F | GRCh38.p7 | 19:8523849 | TTTTAGGCTAGGCGC[A/G]GTGGCTCACGCCTGT | 4542 |
rs62119398 | snp | C/T | 0.155325 | 0.23138 | intron-variant | MYO1F | GRCh38.p7 | 19:8523947 | AACATAGTGAAACTC[C/T]GCCTCTACTAAAAAT | 4542 |
rs62119399 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526335 | CCGTCTTAAAAAAAC[A/C]ACAAAACTCAAAAGT | 4542 |
rs62119400 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8557792 | CTCACTTCCTGCCAG[A/C]CTCCCAGCCTCTCCC | 4542 |
rs62119401 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559977 | AAAAAAAAAAGTAAA[G/T]AATTAACACTCAGCG | 4542 |
rs62119402 | snp | C/G | 0.478271 | 0.101943 | intron-variant | MYO1F | GRCh38.p7 | 19:8560698 | TCCTGGTCTCAGCCT[C/G]CTGTGTAGCTGAGAC | 4542 |
rs62119405 | snp | C/T | 0.466618 | 0.124806 | intron-variant | MYO1F | GRCh38.p7 | 19:8566268 | TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 4542 |
rs62119406 | snp | G/T | 0.44306 | 0.158832 | intron-variant | MYO1F | GRCh38.p7 | 19:8569818 | GGAATGGAGGGTCAT[G/T]GTCCTGGAGGGATAG | 4542 |
rs62119407 | snp | A/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8570691 | TTTTTTTTTTTTTAA[A/T]TAGAGACAAAGTCTA | 4542 |
rs62119436 | snp | A/G | 0.434543 | 0.168653 | intron-variant | MYO1F | GRCh38.p7 | 19:8573180 | GCCAGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC | 4542 |
rs62119437 | snp | C/T | 0.109108 | 0.206518 | intron-variant | MYO1F | GRCh38.p7 | 19:8573943 | GCAGCAGTCACCAGT[C/T]CTATCCTGTTCAAAA | 4542 |
rs71175875 | in-del | -/A | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8560756 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 4542 |
rs71211297 | multinucleotide-polymorphism | CC/TG | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8556138 | GGTTCAAGCGATTCT[CC/TG]TGCCTCAGCCTCCCG | 4542 |
rs71399862 | snp | A/C | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8556153 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 4542 |
rs71399863 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8556185 | AGGTGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 4542 |
rs73002701 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8523016 | GCTTTTTTAAGCATA[A/T]TTTTAAAATTATTTT | 4542 |
rs73004510 | snp | G/T | 0.214206 | 0.248941 | intron-variant | MYO1F | GRCh38.p7 | 19:8534294 | TAGCACAGTTAAACC[G/T]TTGGCTATTTTTCTT | 4542 |
rs73004514 | snp | A/G | 0.00261377 | 0.0360562 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8548249 | TACCTGGAAGATCTC[A/G]AAGCCGTAAATGTCC | 4542 |
rs73004516 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8549508 | CATTAAAAAAGTTTT[C/T]ATTTTATTTATTTAT | 4542 |
rs73004532 | snp | A/G | 0.481627 | 0.0940692 | intron-variant | MYO1F | GRCh38.p7 | 19:8566123 | AAACCCAAACACCAA[A/G]CTAGCACTTATTCTG | 4542 |
rs73004535 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8567042 | CTGGCTGAGGTTAGT[C/T]CTATCACTGGGTCCA | 4542 |
rs73004540 | snp | A/G | 0.108755 | 0.206276 | intron-variant | MYO1F | GRCh38.p7 | 19:8572093 | AGATTGCTGACAGTC[A/G]GTGGCTACCGTCTCA | 4542 |
rs73501537 | snp | A/G | 0.156282 | 0.231769 | intron-variant | MYO1F | GRCh38.p7 | 19:8550725 | GGCAGAAACTGTGCC[A/G]TGAATCCTGGCCTCC | 4542 |
rs73501539 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | MYO1F | GRCh38.p7 | 19:8552782 | GACTTTCACTGGGCC[C/T]AGCGCAGCACCCACA | 4542 |
rs73501540 | snp | C/T | 0.036473 | 0.130024 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8555752 | GTCATCCACGCCGCT[C/T]TGCTTCACGTTGTGG | 4542 |
rs73501543 | snp | A/C/T | 0.0598014 | 0.162251 | intron-variant | MYO1F | GRCh38.p7 | 19:8555842 | CCTTGCACGGGGATG[A/C/T]GGCACCTGGCTCACC | 4542 |
rs73501545 | snp | A/G | 0.41023 | 0.191902 | intron-variant | MYO1F | GRCh38.p7 | 19:8555939 | CCAGGAGAGGCTGGC[A/G]GGGTCCAAGCCAGGC | 4542 |
rs73501558 | snp | G/T | 0.152334 | 0.230133 | intron-variant | MYO1F | GRCh38.p7 | 19:8563444 | CTGGGATTATAGGCG[G/T]GCACCACCACGCCCA | 4542 |
rs73501559 | snp | C/G | 0.153997 | 0.230832 | intron-variant | MYO1F | GRCh38.p7 | 19:8567797 | GTATCAGAGATCGCC[C/G]GGGTTGCTGCTGAGG | 4542 |
rs73922133 | snp | C/T | 0.0173475 | 0.0915031 | synonymous-codon | MYO1F | GRCh38.p7 | 19:8522669 | CACGTTGAGGAATTC[C/T]GTGTTGTGCTCTGAG | 4542 |
rs73922151 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | MYO1F | GRCh38.p7 | 19:8564617 | TCAACCCTGAAGAGC[A/G]TCTGAGCTCACTGGA | 4542 |
rs73922154 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | MYO1F | GRCh38.p7 | 19:8574080 | ATAACAGCAACCACC[A/G]ATGGTCATCATTCCA | 4542 |
rs74178105 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8524408 | GGCAACAGGGCTAGA[C/T]TCTGTCTCAAAAAAA | 4542 |
rs74178106 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8551439 | TCACTGCAACTTCCA[C/T]CTCCCGTTTTCAAGC | 4542 |
rs74178107 | snp | A/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8564143 | CCCAGCACTTTGGGA[A/G]GCCAAGGTGGATGGA | 4542 |
rs74178108 | snp | C/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8574170 | ATTAAACACCAACCG[C/G]CACCACCACCAGCCC | 4542 |
rs74367415 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8532532 | TGCTTGAGAAACATC[A/C]TACTTCAAAGAGAAA | 4542 |
rs74436475 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | MYO1F | GRCh38.p7 | 19:8558005 | GTGCCTGTGTATGAC[C/T]TTGTTCCTCAGCTCT | 4542 |
rs74459657 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | MYO1F | GRCh38.p7 | 19:8558132 | AGGTTGCCATTTTTT[C/T]CATTTCATTTCCTCT | 4542 |
rs74462698 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8548601 | TATTTTCTTTTTTTT[C/T]TTTTCTTTTTTTTTT | 4542 |
rs74493937 | snp | G/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8521824 | TAAAAGTTTTTTTTT[G/T]GTAAATCTTTTGTAG | 4542 |
rs74611388 | snp | A/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8532903 | AGAAAAAAAAAAAAA[A/T]ACACACACACACACA | 4542 |
rs74619257 | snp | G/T | 0.089084 | 0.191327 | intron-variant | MYO1F | GRCh38.p7 | 19:8537143 | TGGATACAGTCCCAA[G/T]AGACAGAGACTGGGG | 4542 |
rs74629306 | snp | A/C | 0 | 0 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526333 | CTCCGTCTTAAAAAA[A/C]CCACAAAACTCAAAA | 4542 |
rs74631841 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8571538 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGACT | 4542 |
rs74744323 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543996 | GTGCTGGTGGTGGTG[C/G]TGGTGGTGGCGGTGG | 4542 |
rs74768935 | snp | C/T | 0.000803334 | 0.0200255 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536452 | ACAGGCCTGGCTGGG[C/T]GTTCTGATGAAGGGG | 4542 |
rs74808663 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8546378 | TTGCTTTTTTTTTTT[G/T]AGACCGGGTTTTGCT | 4542 |
rs75027791 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574166 | CAACATTAAACACCA[A/G]CCGCCACCACCACCA | 4542 |
rs75058013 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | MYO1F | GRCh38.p7 | 19:8565716 | TCAGTGGGTGGGGAC[A/G]CGGGAAGTGCATTTT | 4542 |
rs75107228 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8534110 | CTTGAACCAGGAAGG[C/T]GGAGGTTGCAGTGAG | 4542 |
rs75366391 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | MYO1F | GRCh38.p7 | 19:8535414 | TTATATAGTCTTTGC[C/T]GGTGATAGTTATTTT | 4542 |
rs75513910 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | MYO1F | GRCh38.p7 | 19:8538959 | AACCATATGAATGCA[C/T]TTAATACCACTGAAC | 4542 |
rs75582557 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8535697 | TTTCTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 4542 |
rs75679944 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8536886 | GGGAGGTGTCTCGGT[C/G]AGTTCTAGGGGTAAC | 4542 |
rs75747242 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | MYO1F | GRCh38.p7 | 19:8553540 | GTGCCTGCCAGTATT[C/T]CGGGTACTGGGGATA | 4542 |
rs75858056 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8572015 | GGCGTAAGCCACCGC[A/G]CCTGGCCTTTATACG | 4542 |
rs75917138 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8533037 | GCTAAGAGCCTTGCT[C/G]CCTGCTCTGCTGACC | 4542 |
rs75948259 | snp | G/T | 0.0108287 | 0.072781 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536467 | CGTTCTGATGAAGGG[G/T]ATGGCGAGGGCGGGG | 4542 |
rs76005914 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8565495 | TGTAGTGAGCCAAGA[C/T]TGTGCCATTGCAAGC | 4542 |
rs76017600 | snp | A/C | 0.5 | 0 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526345 | AAAACCACAAAACTC[A/C]AAAGTCTCTCTCTCT | 4542 |
rs76040706 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | MYO1F | GRCh38.p7 | 19:8564548 | GTCAGAGGCAAAACC[C/T]GGACCAGGCAGGGGA | 4542 |
rs76181887 | snp | C/T | 0.0944967 | 0.195752 | intron-variant | MYO1F | GRCh38.p7 | 19:8532758 | CTGAGGGTGATGGCA[C/T]GCATGTGTAGTCCCA | 4542 |
rs76234175 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8540785 | TAAACGTCATGGATT[G/T]AGACACTGCTTAAAG | 4542 |
rs76246227 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543702 | GTGGTGGTGGTGGTG[C/G]TGGTGCTGGTGGTGG | 4542 |
rs76290679 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8537812 | ATAGTTCACTGTAGC[C/G]TCAGCCTCCTGTGCT | 4542 |
rs76305252 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8535431 | GTGATAGTTATTTTT[C/G]TTTTTTCTTTTTGTC | 4542 |
rs76334555 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8571539 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 4542 |
rs76492781 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8533373 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 4542 |
rs76644197 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | MYO1F | GRCh38.p7 | 19:8545960 | AAATACCCCAGCTCC[C/T]TCGCTTCTCCGCTCT | 4542 |
rs76653224 | snp | G/T | 0.158962 | 0.232835 | intron-variant | MYO1F | GRCh38.p7 | 19:8571667 | CAGTGGCGCCATCTC[G/T]GCTCACTGCAAGCTC | 4542 |
rs76733250 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8522022 | AATGTCAGTCAGGGT[C/T]CTTTTTTTTTTTTTT | 4542 |
rs76741544 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8544000 | TGGTGGTGGTGCTGG[C/T]GGTGGCGGTGGCGGT | 4542 |
rs77215905 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8554921 | GGGCGCGGTGGCTCA[G/T]GCCTGTAATCCCAGC | 4542 |
rs77257182 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8539779 | AGCTCCCTAAACCCA[C/G]AGCTGGAGGAAGACC | 4542 |
rs77275384 | snp | C/T | 0.046775 | 0.145601 | intron-variant | MYO1F | GRCh38.p7 | 19:8543375 | TAGGAGGCTTCAGCA[C/T]ATTTTGAAGGCTGGT | 4542 |
rs77382565 | snp | C/G | 0 | 0 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578592 | TTCCTGGATGACTTA[C/G]TTACTCCCTTTTCTC | 4542 |
rs77496349 | in-del | -/TT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8560740 | CCACCACGCCTGGCT[-/TT]AATTTTTTTTTTTTT | 4542 |
rs77590279 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | MYO1F | GRCh38.p7 | 19:8554413 | GGCAAACCTCCCTGG[A/G]GGTGGTGATGTTTCA | 4542 |
rs77618573 | snp | C/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543990 | GTGCTGGTGCTGGTG[C/G]TGGTGCTGGTGGTGG | 4542 |
rs77825772 | snp | C/T | 0.185472 | 0.241529 | intron-variant | MYO1F | GRCh38.p7 | 19:8562048 | TTTTTTCTTTTGTTT[C/T]TTTTGAGATGGAGTC | 4542 |
rs77853209 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | MYO1F | GRCh38.p7 | 19:8568778 | ATACAAAAATTAGCC[C/T]GGCGTGGTGGCGGGT | 4542 |
rs77889622 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8531853 | CCGGGTGCAGTGGCT[C/T]AAGCCTGTAATCCCA | 4542 |
rs77971906 | snp | A/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8537994 | TATTTTTATTTGGAG[A/G]CAAAATCTCGCTCTG | 4542 |
rs78144891 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8557679 | CATGAAGGATGCCAG[G/T]CTTGGCGGGCAGGGC | 4542 |
rs78236562 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | MYO1F | GRCh38.p7 | 19:8564599 | GGGTTAGGAGCCATC[G/T]ACTCAACCCTGAAGA | 4542 |
rs78398748 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MYO1F | GRCh38.p7 | 19:8524767 | CCTCCTCCTATCCTC[C/T]GTAGGAGAGCTTCTG | 4542 |
rs78478432 | snp | A/G | 0.000314682 | 0.0125396 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8548279 | CAGCACACCGATGCT[A/G]TACTCTTCCTGGGGT | 4542 |
rs78543795 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539856 | GGTAGACAGACAGAC[A/G]TTGGAATGAGAGAAA | 4542 |
rs78709087 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | MYO1F | GRCh38.p7 | 19:8540154 | ATGTGGAGGGGAGCT[A/G]TGATGGGTGAGATGC | 4542 |
rs78797234 | snp | A/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8571384 | TCAGGGGAGCAGGGG[A/G]ACTGGACTCTGTTTC | 4542 |
rs78882643 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8546377 | CTTGCTTTTTTTTTT[G/T]GAGACCGGGTTTTGC | 4542 |
rs78936828 | snp | A/G | 0.0444908 | 0.142359 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536085 | TCAACCTCTATCTCA[A/G]TTTCTCTGTCAATCC | 4542 |
rs78946364 | snp | C/T | 0.144632 | 0.226711 | intron-variant | MYO1F | GRCh38.p7 | 19:8562309 | CCGGCCCTTCCTTTC[C/T]TTTTCTTGTCTTTTT | 4542 |
rs79007509 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8571254 | GCTCCCAGACCCTGC[C/T]CTGGTGCCTGAGGGT | 4542 |
rs79180777 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | MYO1F | GRCh38.p7 | 19:8547892 | AGAAGGAAGTATCAC[C/T]ATGGAGCCTGGGTAG | 4542 |
rs79190325 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8531852 | GCCGGGTGCAGTGGC[G/T]CAAGCCTGTAATCCC | 4542 |
rs79235764 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8540284 | CCTGGGCTCAAGCCA[A/G]TGTGTGAATGTATTG | 4542 |
rs79335539 | snp | G/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8522041 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 4542 |
rs79348958 | snp | C/T | 0.143284 | 0.226079 | intron-variant | MYO1F | GRCh38.p7 | 19:8563084 | GTAACCTCTGCCTCC[C/T]GGGTCCAAGTGATTG | 4542 |
rs79352255 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8558963 | GGCTCACTGCTACCT[C/T]TGCCTGCGGGGCTCA | 4542 |
rs79405287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8564568 | CAGGCAGGGGAGGCC[C/T]AGATGGGACGAGGGT | 4542 |
rs79443223 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8540307 | ATGTATTGAATGCCA[C/T]TGAATTGTACATTTC | 4542 |
rs79504417 | snp | C/T | 0.030665 | 0.119967 | intron-variant | MYO1F | GRCh38.p7 | 19:8565434 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 4542 |
rs79574013 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | MYO1F | GRCh38.p7 | 19:8562613 | TAATCATAGCTAACT[A/G]TAGCCTTGACGTCCA | 4542 |
rs79609735 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8554916 | TGGCCGGGCGCGGTG[G/T]CTCATGCCTGTAATC | 4542 |
rs79646756 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8537900 | TGCCTGGCTAAGACA[C/T]GTACTTTGGAGGTAG | 4542 |
rs79662401 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | MYO1F | GRCh38.p7 | 19:8537249 | CCACACTAGTGGGAC[C/T]GATGTGGGGTGTCTG | 4542 |
rs79734627 | snp | A/G/T | 0.000875516 | 0.0209046 | intron-variant | MYO1F | GRCh38.p7 | 19:8555800 | CTCCTTGCTGCCCTG[A/G/T]GGGGTGAGAGGGGGG | 4542 |
rs79764725 | snp | G/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8570091 | CATTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 4542 |
rs79781467 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8543248 | GAACTTCTGCTCTCA[G/T]GTTGTGAGATCCTTG | 4542 |
rs79873183 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | MYO1F | GRCh38.p7 | 19:8538828 | TGTCACATTCATAGC[A/G]ACAGAATGGTGAGTG | 4542 |
rs79980665 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8563920 | AGGCATGAGCCACTG[C/T]GCTTTGGCCTGACCC | 4542 |
rs79984057 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8522039 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 4542 |
rs79984981 | in-del | -/TT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8538603 | TTTTTTTTTTTTTTT[-/TT]AAGAGACAGGGTCTC | 4542 |
rs80079374 | snp | C/G/T | 0.0171124 | 0.0909042 | intron-variant | MYO1F | GRCh38.p7 | 19:8550724 | GGGCAGAAACTGTGC[C/G/T]GTGAATCCTGGCCTC | 4542 |
rs80155306 | snp | C/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8552722 | AGGCTACACAGCTCA[C/G]AGTGATAGAATCAAA | 4542 |
rs80179082 | snp | C/G | 0.0106087 | 0.0720543 | intron-variant | MYO1F | GRCh38.p7 | 19:8554458 | AGCAGGGTCTGTGGC[C/G]CCCCAACTCTGTCCA | 4542 |
rs80275520 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | MYO1F | GRCh38.p7 | 19:8555977 | CCCAGACAGAAGTTG[C/G]ACTGCTCGGATCCAG | 4542 |
rs111295514 | snp | A/G | 0.106278 | 0.204558 | intron-variant | MYO1F | GRCh38.p7 | 19:8549063 | TCAAGAGATTCTTCT[A/G]CCTCAGCCTCCCAAG | 4542 |
rs111296389 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8556007 | GCCCTCAGCCCTCTA[C/T]TTTTTTTTAATTTTT | 4542 |
rs111304826 | snp | C/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8536718 | CTGAGGGAAGTTTGG[C/G]GGGTGAGTTCTGTGG | 4542 |
rs111309880 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MYO1F | GRCh38.p7 | 19:8524816 | TAAATAAGAGCTCAA[C/T]GAATGGAATGGGAAT | 4542 |
rs111323682 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8560648 | GGCAAGGTCATGGCT[C/T]ACTGCAGCCTTGACC | 4542 |
rs111393660 | snp | C/T | 0.158632 | 0.232706 | intron-variant | MYO1F | GRCh38.p7 | 19:8556328 | AGCCACCGCACCCGG[C/T]CTCTTTTTTTTTTAA | 4542 |
rs111418585 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MYO1F | GRCh38.p7 | 19:8531748 | ACTCGACACTATCCA[C/T]GAGGTACACTGCCGT | 4542 |
rs111477047 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8529510 | ATGTATCCCTGTAGA[C/G]AGCATGTACCTATGG | 4542 |
rs111486936 | snp | C/T | 0.335559 | 0.234904 | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520418 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA | 4542 |
rs111505144 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | MYO1F | GRCh38.p7 | 19:8557056 | TTTGGGAGGCCGAGG[C/T]GGGAGGACTGCTTAA | 4542 |
rs111510988 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8541425 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTTTTTTTT | 4542 |
rs111515270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8569431 | AACTAGGGCAGGCGG[A/G]GACAACCTTCCTGGT | 4542 |
rs111542097 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | MYO1F | GRCh38.p7 | 19:8527265 | TGTCAGGGTAACAGA[C/T]GGGGTCACTAGAATG | 4542 |
rs111569539 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8531893 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 4542 |
rs111594115 | snp | A/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8564103 | AAGTGGGTGCTGGCC[A/G]GGCATGGCGGCTCAT | 4542 |
rs111602347 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8568275 | AAAACTACAAAAAAT[C/T]AGCCAGGTGCGGTGG | 4542 |
rs111609261 | snp | C/T | 0.308908 | 0.242961 | intron-variant | MYO1F | GRCh38.p7 | 19:8524113 | AACAGAGCAAGACAC[C/T]GTCTCAAAAAAAAAA | 4542 |
rs111642569 | snp | A/G | 0.160938 | 0.233598 | intron-variant | MYO1F | GRCh38.p7 | 19:8545369 | GCTGGGATTACAGGC[A/G]TGAGCCACCGGCATG | 4542 |
rs111644945 | snp | A/G | 0.157311 | 0.232183 | intron-variant | MYO1F | GRCh38.p7 | 19:8560197 | AACAGCAAAGAACAG[A/G]TTCTTGGCTGGGCGC | 4542 |
rs111647273 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8568355 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 4542 |
rs111656074 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534510 | TGGGGTTTCCCCATG[G/T]TGGCCAGGCTGGTCT | 4542 |
rs111676269 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | MYO1F | GRCh38.p7 | 19:8532296 | GAAAGCAGAGAAAAG[C/G]GTTTTGAGTTGTAAA | 4542 |
rs111740323 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8550469 | CCACATTTTTTTCCT[C/G]GTGGGCTTTCAGCTT | 4542 |
rs111751676 | snp | C/T | 0.123452 | 0.215605 | intron-variant | MYO1F | GRCh38.p7 | 19:8538078 | CCAGGTTCAAGTGAT[C/T]CTCCCACCTCAGCCT | 4542 |
rs111752144 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | MYO1F | GRCh38.p7 | 19:8568392 | GGTGCCACTGCAGTC[C/T]GGCCTGGGTGAAAGA | 4542 |
rs111752628 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8533357 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 4542 |
rs111752889 | in-del | -/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8534630 | TTTTCATTTTACTAA[-/T]TTTTTTTTTTTTTGA | 4542 |
rs111757104 | in-del | -/T | 0.460854 | 0.134315 | intron-variant | MYO1F | GRCh38.p7 | 19:8563516 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTGAGATG | 4542 |
rs111852383 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543894 | GTGGTGGTGGTGGTG[A/G]TGCTGGTGGTGGTGG | 4542 |
rs111876717 | snp | A/G | 0.338069 | 0.233974 | intron-variant | MYO1F | GRCh38.p7 | 19:8549564 | GTTGCCCAGGCTGGA[A/G]TACAATAGCACGATC | 4542 |
rs111995464 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8540649 | CAGGAGGTGGAGGTT[A/G]CAGTGAGCCGAGATC | 4542 |
rs112088495 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8529661 | TAGGCAAGGGTGGCC[C/T]CGTGGTTGGGGCTTC | 4542 |
rs112090287 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | MYO1F | GRCh38.p7 | 19:8550784 | ACCACAGCACGGACT[C/T]AGGGAGTGAGCACCC | 4542 |
rs112090355 | snp | A/T | 0.123452 | 0.215605 | intron-variant | MYO1F | GRCh38.p7 | 19:8538200 | TCAACTCCTGACCTC[A/T]GGTGATCCACCTGCC | 4542 |
rs112150607 | in-del | -/T | 0.0182935 | 0.0938728 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526641 | GGGCGCTGGCTGAGG[-/T]TCCCCCGCCCCACCC | 4542 |
rs112163085 | snp | A/G | 0.39709 | 0.20215 | intron-variant | MYO1F | GRCh38.p7 | 19:8546756 | CAATCTCGACTCACT[A/G]CAAGCTCTGCCTCCT | 4542 |
rs112181087 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8530926 | GTAGATGCCTGTGAT[C/T]CCAGCTACTCGGGAG | 4542 |
rs112187537 | snp | A/C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8525110 | GAGGCTGAGGCAGGA[A/C/G]AATCGCTTGAATCCA | 4542 |
rs112197280 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | MYO1F | GRCh38.p7 | 19:8576953 | GCTACACAGGGAGAC[C/G]AGAGACTGGGCTGGA | 4542 |
rs112280342 | snp | A/G | 0.337841 | 0.23406 | intron-variant | MYO1F | GRCh38.p7 | 19:8546749 | AATGGCACAATCTCG[A/G]CTCACTACAAGCTCT | 4542 |
rs112342819 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8533243 | CATGTTGTCCAGACT[C/G]GTCTGGAACTCCTGG | 4542 |
rs112379785 | snp | A/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8571082 | GCAACTCACCCCATG[A/G]GCTCCAGGCTGTCTG | 4542 |
rs112415550 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | MYO1F | GRCh38.p7 | 19:8570319 | AGGCAATCCACTCAT[A/C]TCGGCCTCCCAAAGT | 4542 |
rs112422651 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | MYO1F | GRCh38.p7 | 19:8530829 | TGGATCACCTGAGGT[C/G]AGGAGTTTGAGACGA | 4542 |
rs112456965 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | MYO1F | GRCh38.p7 | 19:8534942 | TTTTACTAAAATTAA[A/G]TTACTGTTGCCCAGG | 4542 |
rs112458917 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8530732 | CTTTCTAGTGACACT[C/G]GTTCATAAAGAAAAG | 4542 |
rs112538078 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | MYO1F | GRCh38.p7 | 19:8564178 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 4542 |
rs112548189 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | MYO1F | GRCh38.p7 | 19:8524481 | TCCCAGCTACTCAGG[C/G]GGCTGAGGCAGGAGA | 4542 |
rs112601546 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543885 | GTGGTGCTGGTGGTG[G/T]TGGTGGTGGTGCTGG | 4542 |
rs112625942 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8533360 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTGAG | 4542 |
rs112630616 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MYO1F | GRCh38.p7 | 19:8545470 | AGGTGGACAAGTAGG[C/T]GGAATGAATGGATGA | 4542 |
rs112640311 | snp | C/T | 0.0149554 | 0.0851705 | intron-variant | MYO1F | GRCh38.p7 | 19:8553325 | GAGGGCGACCCAGCT[C/T]ATCCTTCTGTTTTCC | 4542 |
rs112650392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8531224 | TGGTGGCACATGCCT[A/G]TAATACCAGCTACTC | 4542 |
rs112686108 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | MYO1F | GRCh38.p7 | 19:8531050 | ACTCCATCTCAAAAA[A/G]ACAAAAAACAAAAAC | 4542 |
rs112689568 | snp | C/T | 0.0178098 | 0.0926698 | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520754 | CAGTAGCTGGGATTA[C/T]AGGCAGGCACCACCA | 4542 |
rs112788465 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | MYO1F | GRCh38.p7 | 19:8535273 | TCAGTCTGTCTTTGT[C/T]GTTGATGTTCTTATA | 4542 |
rs112789212 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | MYO1F | GRCh38.p7 | 19:8534048 | GCCTGGTGTGGTGGC[A/G]GGTGCCTGTAATTCC | 4542 |
rs112827466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8564975 | ACAGGATTTCACCAC[A/G]TTGGACACGCTCATC | 4542 |
rs112887894 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | MYO1F | GRCh38.p7 | 19:8546500 | GAGTAGCTGGGACCG[C/T]AGGAGCACACCACCA | 4542 |
rs112893439 | snp | G/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8553914 | CTCTCTCTCTCTCTC[G/T]CTCTCTCTCGCTCTC | 4542 |
rs112981681 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | MYO1F | GRCh38.p7 | 19:8572492 | AGACTGGTCTCGAAC[A/T]CCTGACCTCAAGTGA | 4542 |
rs112997941 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8531240 | TAATACCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 4542 |
rs113039068 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577495 | AGGGGCCGAGGCCAT[C/G]GGGGAGGGAAGCTGG | 4542 |
rs113056059 | snp | C/G/T | 0 | 0 | splice-donor-variant, intron-variant | MYO1F | GRCh38.p7 | 19:8545649 | TTGACCCAGCCCTCA[C/G/T]CAGCTTGTTTTCGAT | 4542 |
rs113057816 | in-del | -/AGAA | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8556516 | GAAAGAGAAAGAAAG[-/AGAA]AGAAAGAAAGAAAGA | 4542 |
rs113131174 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | MYO1F | GRCh38.p7 | 19:8546959 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 4542 |
rs113135093 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8532728 | CCGTCTCTACAAAAA[A/C]TAAGCAAAAATTAGC | 4542 |
rs113189372 | snp | A/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8523269 | CGATCTCCTGACCTT[A/G]TGATCCGCCCGCCTT | 4542 |
rs113214325 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | MYO1F | GRCh38.p7 | 19:8535200 | TACAGGTGTGAGCCA[C/G]TGCGCCTGGCCAGCA | 4542 |
rs113280803 | snp | C/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8573308 | AGAGCGAGACTCTGT[C/G]TCAAAAAAAAAAGAA | 4542 |
rs113312019 | snp | A/G | 0.162253 | 0.234095 | intron-variant | MYO1F | GRCh38.p7 | 19:8555295 | GAATCATTTGAATCC[A/G]GGAGGTGGAGGTTGC | 4542 |
rs113331627 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8532997 | ACCCAGAGTGCTTTC[A/C]CAAGTCCATAGGTAG | 4542 |
rs113344276 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | MYO1F | GRCh38.p7 | 19:8575497 | GAGGAGGTGGAGCTC[A/G]GGCTTGCTTGCCTGC | 4542 |
rs113378543 | snp | A/G | 0.21695 | 0.247806 | intron-variant | MYO1F | GRCh38.p7 | 19:8531138 | AGATCGCCTGAGGTC[A/G]GGAGTTTGAGACCAG | 4542 |
rs113395896 | snp | A/G | 0.139225 | 0.224118 | intron-variant | MYO1F | GRCh38.p7 | 19:8540101 | TCCTCCAGGGGTGGG[A/G]CAGCCTCAATGCCGC | 4542 |
rs113402443 | snp | C/G | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8559667 | TTGAAAGAATTAACA[C/G]GACCGGGCGCGGTGG | 4542 |
rs113430749 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8557766 | TGGTGGGAAGTGGGC[A/G/T]CATCCCAGTTCTCAC | 4542 |
rs113446543 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | MYO1F | GRCh38.p7 | 19:8549199 | TTGGGTGATCTGCCC[A/G]CTTTGACCTCCCAAA | 4542 |
rs113482980 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8527953 | GGAGGGCTGGGTGCC[A/G]TGGCTCACGCCTGTA | 4542 |
rs113510643 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | MYO1F | GRCh38.p7 | 19:8576632 | TGACAGGCAGCAACA[A/C]CTCTGGCTGCCATCC | 4542 |
rs113521200 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8576181 | TTTTGTATTTTTTAG[G/T]AGAGACGAGGTTTCA | 4542 |
rs113531654 | in-del | -/A | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8555939 | CCAGGAGAGGCTGGC[-/A]GGGTCCAAGCCAGGC | 4542 |
rs113562766 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8529596 | GGTGAAGGTATATCT[A/G]ATTTCCAGGTTGAAG | 4542 |
rs113576178 | snp | G/T | 0.235273 | 0.249566 | intron-variant | MYO1F | GRCh38.p7 | 19:8531128 | TGAGGCGGGAAGATC[G/T]CCTGAGGTCGGGAGT | 4542 |
rs113632269 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8533132 | GCGATCTCGGCTCCC[A/G]GGCTCAAGGGATCCT | 4542 |
rs113634244 | snp | C/T | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8572279 | TGGGCATTTTTTTTT[C/T]CCCTCTGAGACAGAG | 4542 |
rs113664957 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8547033 | CTGGGCATATTAACT[C/G]ATGCCTGTAGTCCCA | 4542 |
rs113668631 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | MYO1F | GRCh38.p7 | 19:8545075 | GAGCCACCATGTCCC[A/G]CCTAAATACGTCTTA | 4542 |
rs113669128 | snp | A/C/G | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8530820 | CGAGGCGGGTGGATC[A/C/G]CCTGAGGTCAGGAGT | 4542 |
rs113690085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8539312 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 4542 |
rs113701057 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8533290 | AGCCTTGACCTCCCA[A/G]AGTGCTGGGATTACA | 4542 |
rs113747967 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | MYO1F | GRCh38.p7 | 19:8531119 | TTGGGAGGCTGAGGC[A/G]GGAAGATCGCCTGAG | 4542 |
rs113833574 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8531295 | GAGGTTGCGGTGAGC[C/T]GAGATTGTGCCATTG | 4542 |
rs113898159 | snp | C/T | 0.232943 | 0.249417 | intron-variant | MYO1F | GRCh38.p7 | 19:8524146 | AAAAAAAAGGCCGGG[C/T]GCGGTGGCTCACACC | 4542 |
rs113900022 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | MYO1F | GRCh38.p7 | 19:8561025 | TATAGGTGTGAGCCA[C/T]TGCGCCTGGCCACGC | 4542 |
rs113906911 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | MYO1F | GRCh38.p7 | 19:8533906 | AATCAAAATAGGGGC[C/T]GGGCGCGGTGGCTCA | 4542 |
rs113939769 | snp | C/T | 0.5 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8575981 | TTTGGGTGTGAATTC[C/T]GGGATGCCCAATTTC | 4542 |
rs113971024 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | MYO1F | GRCh38.p7 | 19:8565064 | AGGCATGAGCCACTG[C/T]GTCCGGCCAGAGACA | 4542 |
rs113986837 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | MYO1F | GRCh38.p7 | 19:8535019 | TGGGTTAAAGTGATT[C/T]TCCTGCCTCAGCCTC | 4542 |
rs114019354 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | MYO1F | GRCh38.p7 | 19:8549360 | CACTACAGCCTCAAC[C/T]TCCTGGGGTCAGGGA | 4542 |
rs114026321 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8542050 | GGCTGGGAGGGTGGG[C/T]GTGGGGTGCTTACAG | 4542 |
rs114092933 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | MYO1F | GRCh38.p7 | 19:8558689 | ACTTGGAGCTACCCC[A/G]TTTGGTGAACTGATG | 4542 |
rs114095677 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | MYO1F | GRCh38.p7 | 19:8538112 | GAGTAGCTGCCACCA[C/T]ACCCAGCTCCTTTTT | 4542 |
rs114211438 | snp | G/T | 0.00529323 | 0.0511722 | intron-variant | MYO1F | GRCh38.p7 | 19:8530611 | AAGGGTGAGTCCTGG[G/T]GTCTCCCCAGGGGCT | 4542 |
rs114242403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8540210 | TTTGAGGCAGGGCCT[C/T]GCTTTGTCCTCCAGG | 4542 |
rs114453023 | snp | A/T | 0.0515638 | 0.152063 | intron-variant | MYO1F | GRCh38.p7 | 19:8538130 | CCAGCTCCTTTTTTT[A/T]TATATATATATTTTT | 4542 |
rs114581850 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8540712 | GAGAGACACTGTCTC[A/C]AAAAAAAAAAAAAAA | 4542 |
rs114612073 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | MYO1F | GRCh38.p7 | 19:8535343 | ATTTCTACCCCGTCC[A/G]TCTTCTCCAAATCAA | 4542 |
rs114632106 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MYO1F | GRCh38.p7 | 19:8574136 | TCCAGCTGAAAACAA[C/T]CCACCACCAACGAAC | 4542 |
rs114767281 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | MYO1F | GRCh38.p7 | 19:8545932 | GACCAATAATCAACA[A/G]GAGTGGGTGGATAAA | 4542 |
rs114770895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8575640 | AGAAATACTGTTTCA[C/T]TGAATCCTTCAGCGA | 4542 |
rs114879819 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | MYO1F | GRCh38.p7 | 19:8571986 | CCTCGGCCTCCTAAA[A/G]TATTGGGATTACAGG | 4542 |
rs114882772 | snp | A/C/T | 0.0162398 | 0.0886349 | intron-variant | MYO1F | GRCh38.p7 | 19:8546011 | AGTGCAGTTGCATTC[A/C/T]GGTTGTCCACAGCAT | 4542 |
rs114907713 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MYO1F | GRCh38.p7 | 19:8529292 | TCTGGGACATGAGAT[A/G]TGGGTCAAGTGAGTG | 4542 |
rs114938556 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539818 | CAGATGACGTCACAG[A/T]CAGAGGCAGAAGCCC | 4542 |
rs114942456 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8545084 | TGTCCCGCCTAAATA[C/T]GTCTTAAATTTAATT | 4542 |
rs114946243 | snp | G/T | 0.00286376 | 0.0377317 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8526894 | TCCAGGAAGCTGTCG[G/T]CGGCATCCTCTTGGA | 4542 |
rs114995767 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | MYO1F | GRCh38.p7 | 19:8541672 | GGCCTCAAGAGATTT[A/G]TCCACTTCGGCCTCC | 4542 |
rs115006719 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYO1F | GRCh38.p7 | 19:8524963 | AGCACTTTCGGAGGC[C/T]GAGACGGGCGGGTCA | 4542 |
rs115086862 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8538441 | GATTACAGGCATATG[C/T]TGGCTAAATTTTGTA | 4542 |
rs115088972 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | MYO1F | GRCh38.p7 | 19:8558648 | ATCTCTGCAAAGGAG[C/T]AGTCTGACAGATAGG | 4542 |
rs115152587 | snp | A/C/T | 0.0308354 | 0.12028 | intron-variant | MYO1F | GRCh38.p7 | 19:8540073 | GAGGTATGGCTAGAC[A/C/T]TTCGGGTACTCTTCC | 4542 |
rs115168743 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MYO1F | GRCh38.p7 | 19:8557908 | TTCTCCCTCCTACCT[C/T]TCCTCTTCTCTTGTG | 4542 |
rs115213713 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8542144 | CGCTGGCTGGGGGGT[A/G]TCTACAGTTCAGAAT | 4542 |
rs115441173 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | MYO1F | GRCh38.p7 | 19:8540400 | GGGAACAACACGGAT[A/G]AATTGTACATTTTAA | 4542 |
rs115444888 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | MYO1F | GRCh38.p7 | 19:8562997 | TTCTTTCCTTCTTTC[C/T]TTTTTTTGTTTTGAT | 4542 |
rs115484482 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | MYO1F | GRCh38.p7 | 19:8569230 | TTTGTTTGTAAGTCT[C/G]TTCCTTGGGGGTGGG | 4542 |
rs115485773 | snp | C/T | 0.00284737 | 0.0376242 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8526895 | CCAGGAAGCTGTCGG[C/T]GGCATCCTCTTGGAG | 4542 |
rs115515057 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8533727 | TGGACTTCTGACCTG[A/C/T]GGAACTGTGAGAGAA | 4542 |
rs115528415 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8551212 | GCATGGCATCATACC[C/T]GGCTAATCTTTGTAT | 4542 |
rs115675479 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8541797 | CACAGCCACTCCCCT[C/T]GAGTTTGTGGCGAGA | 4542 |
rs115713483 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | MYO1F | GRCh38.p7 | 19:8546418 | AGGCTGGAACTCAGC[A/G]ATGCGATCCTAGCTC | 4542 |
rs115749861 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8541397 | TTACATCTAATGCTA[C/T]GTTCTTTGTGTGTGT | 4542 |
rs115875216 | snp | A/G | 0.0300714 | 0.118876 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536473 | GATGAAGGGGATGGC[A/G]AGGGCGGGGGTGGAG | 4542 |
rs115988886 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8557175 | CTGTGATCATAGCTA[C/G]TCTGGAAGCTGAGGT | 4542 |
rs116023727 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8540845 | AACCCTTACGTGCAC[A/G]TGGATCCCTGGGAGG | 4542 |
rs116059799 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | MYO1F | GRCh38.p7 | 19:8561822 | CCCAGGTTCAAACGA[C/T]TCTTCTGCCTCAGCC | 4542 |
rs116148118 | snp | A/C/G | 0.0448719 | 0.142907 | intron-variant | MYO1F | GRCh38.p7 | 19:8538578 | TGAGCCATTGCTCCC[A/C/G]GTCTGATTTTTTTTT | 4542 |
rs116302458 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | MYO1F | GRCh38.p7 | 19:8550486 | TGGGCTTTCAGCTTC[C/T]TGGGGGCTGAGCTAG | 4542 |
rs116313178 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8541066 | ACGGCTCACTGTAGC[C/T]TCCACCTCCTAGGCT | 4542 |
rs116398083 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | MYO1F | GRCh38.p7 | 19:8544592 | AGCTTTGGGGGTGGG[A/G]AGGGCACCAGGGGCT | 4542 |
rs116559216 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | MYO1F | GRCh38.p7 | 19:8561444 | CCTCTCCCTCCCTTC[C/T]TTCCTCCCTCTCTCC | 4542 |
rs116615240 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | MYO1F | GRCh38.p7 | 19:8552241 | GGGGATGGGTCTTAT[A/G]AGCCTTGCCTCTCTT | 4542 |
rs116632618 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8538907 | CAGTTTGGGAAGATG[A/G]GAAAGTTCTGGAGAT | 4542 |
rs116642666 | snp | C/T | 0.271162 | 0.249103 | intron-variant | MYO1F | GRCh38.p7 | 19:8574677 | TCTTTCTCTCTTTCT[C/T]TCTTTCTTCCTTTCT | 4542 |
rs116679811 | snp | A/C | 0.120326 | 0.21374 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578072 | CCAAAAAAACAACAA[A/C]AACAGGGAAGGGTGC | 4542 |
rs116704366 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | MYO1F | GRCh38.p7 | 19:8548550 | CAGGGTCCCTGACTC[C/T]AGAGCTGACTCTGCC | 4542 |
rs116787802 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8557568 | CAGTCCCCCAAAGTG[G/T]TGGGATTATAGGCGT | 4542 |
rs116789656 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8521022 | TGAACCTCCATTGTT[C/T]CACCTGTAAGATGGG | 4542 |
rs116966117 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | MYO1F | GRCh38.p7 | 19:8528884 | AGGAAGGCAGGTGAG[A/G]GTGTACCTGGTAGAA | 4542 |
rs117077244 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | MYO1F | GRCh38.p7 | 19:8558693 | GGAGCTACCCCATTT[G/T]GTGAACTGATGGTCA | 4542 |
rs117118593 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MYO1F | GRCh38.p7 | 19:8540255 | TGCGATGATAGGAAC[C/T]GCAGCCTGGAACTCC | 4542 |
rs117162033 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MYO1F | GRCh38.p7 | 19:8562685 | GACCACAGGCAAGTA[C/T]CACTGTGCCCAGCTA | 4542 |
rs117296106 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MYO1F | GRCh38.p7 | 19:8576473 | GAGAAATGAAAGCTG[A/G]AGTGGTCTACACAGC | 4542 |
rs117298671 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | MYO1F | GRCh38.p7 | 19:8531387 | AGGGTCTCGCTCCGT[C/T]GCCCAGACTGGAGTG | 4542 |
rs117378928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8534212 | CATCCCAACATGAAT[A/G]CATTTTTGGTTGAGA | 4542 |
rs117417922 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | MYO1F | GRCh38.p7 | 19:8533728 | GGACTTCTGACCTGC[A/G]GAACTGTGAGAGAAT | 4542 |
rs117506721 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MYO1F | GRCh38.p7 | 19:8556558 | AAGCCATGAAAAGAC[A/G]TGGAGGAAACTTAAA | 4542 |
rs117515581 | snp | C/G | 0.0165278 | 0.0893908 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550572 | CTCACGGTCCACACT[C/G]TCCACTCGGGCGTAA | 4542 |
rs117536602 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYO1F | GRCh38.p7 | 19:8545797 | TGGCCACCCTTCCCC[C/T]CATGTCCTCTCCCCT | 4542 |
rs117551866 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | MYO1F | GRCh38.p7 | 19:8551098 | ACTCTTTCACCCAGG[C/T]GGGAGTGCAGCGGCG | 4542 |
rs117637408 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | MYO1F | GRCh38.p7 | 19:8541368 | AACACTTTAAGGATC[C/T]CCGTCTTATTACTTT | 4542 |
rs117665505 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | MYO1F | GRCh38.p7 | 19:8576602 | CCCGTTGCTATCATC[A/G]ACAGACCTCAGACTT | 4542 |
rs117700741 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | MYO1F | GRCh38.p7 | 19:8572948 | TGATCCTCCCACCTC[C/T]GTCTTCCAAACTGTT | 4542 |
rs117727578 | snp | C/T | 0.00224765 | 0.033448 | intron-variant | MYO1F | GRCh38.p7 | 19:8550157 | AGCCCCAGCCCCACT[C/T]GCCTCCACGAGGAAG | 4542 |
rs117739182 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | MYO1F | GRCh38.p7 | 19:8565532 | GGGCAACAAGTGCGA[A/T]ACTCTGTCTCGAAAT | 4542 |
rs118029702 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | MYO1F | GRCh38.p7 | 19:8569395 | TTCAGAGAGGTCTCT[C/G]TACCCCAAGGCTGAA | 4542 |
rs118094937 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | MYO1F | GRCh38.p7 | 19:8540769 | AATTCTGTGAATTTG[C/T]TAAACGTCATGGATT | 4542 |
rs137859878 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | MYO1F | GRCh38.p7 | 19:8549139 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGC | 4542 |
rs137863578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8528932 | GGTTGAGCTGGCCTG[C/T]GGTCAGAGTTCTCTG | 4542 |
rs137902973 | in-del | -/AAGCCTGT | 0.177824 | 0.239355 | intron-variant | MYO1F | GRCh38.p7 | 19:8531853 | CGGGTGCAGTGGCTC[-/AAGCCTGT]AAGCCTGTAATCCCA | 4542 |
rs137964017 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8542604 | TTTTTGTTTGTTTGC[-/T]TTTTTTTTTTTTTTG | 4542 |
rs138068763 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | MYO1F | GRCh38.p7 | 19:8532170 | CAAAAAAAAAAAGAA[A/G]GAAAAAGAAAATCTG | 4542 |
rs138074525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8561974 | CCCATGTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 4542 |
rs138085662 | in-del | -/ACTGTG | 0.0437281 | 0.141251 | intron-variant | MYO1F | GRCh38.p7 | 19:8538972 | ACTTAATACCACTGA[-/ACTGTG]ACATTAAAACTGGTT | 4542 |
rs138125354 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | MYO1F | GRCh38.p7 | 19:8539270 | AAATACAAAATTAGC[C/T]GGGCATGGTGGTGCA | 4542 |
rs138178012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8537781 | GTCACTCAGGCTGGG[A/G]TATAGTGGCGCCGTG | 4542 |
rs138339626 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | MYO1F | GRCh38.p7 | 19:8571509 | AACCTCCACCTCCTG[G/T]GTTCAAGCGATTCTC | 4542 |
rs138451900 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | MYO1F | GRCh38.p7 | 19:8558416 | AGTGATCCTCCCACC[C/T]CAGCCTCCCAAAGTG | 4542 |
rs138477350 | snp | A/G | 0.00039745 | 0.0140914 | intron-variant | MYO1F | GRCh38.p7 | 19:8554439 | TTTCAGCAGGGGCCC[A/G]GGCAGCAGGGTCTGT | 4542 |
rs138505600 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521258 | CACATGGCAGTTGGG[A/T]GGTAGATTCTGCTGT | 4542 |
rs138586450 | in-del | -/CT | | | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536175 | CCCTCTGTCTCTCTC[-/CT]TCTCTCTCTCAGTCC | 4542 |
rs138718962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8529769 | GCTACAAGTGCATGT[G/T]TGATGGACAGCTGTG | 4542 |
rs138785496 | snp | A/G | 0.238171 | 0.24972 | intron-variant | MYO1F | GRCh38.p7 | 19:8524029 | GAGGCTGAGGCAGGA[A/G]AATTGCTTCAACCTG | 4542 |
rs138792758 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | MYO1F | GRCh38.p7 | 19:8566216 | TTTCTCGCCCAGGCT[A/G]GAGTGCAGTGGCATG | 4542 |
rs138949132 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MYO1F | GRCh38.p7 | 19:8558573 | TTTTAGCCCGACTGA[A/G]TTTATCTAGTGCCTT | 4542 |
rs138953752 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8579348 | CTTTGGGAGGCTGAG[A/G]TGGGAGGATCGCTTG | 4542 |
rs138969920 | snp | C/T | 0.0209421 | 0.100162 | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520442 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 4542 |
rs139061910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8573279 | TCATGCCACTGCACT[C/G]CATCCTGGGTGACAG | 4542 |
rs139182785 | snp | C/T | 0.182296 | 0.240658 | intron-variant | MYO1F | GRCh38.p7 | 19:8545210 | CTCCCACCTCAGCCT[C/T]CCGGGTAGCTGGGAT | 4542 |
rs139197999 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8546221 | AGGTATGTGCCACCA[C/T]GCCGGACTAATTTTG | 4542 |
rs139211736 | snp | C/T | 0.0100238 | 0.0700815 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550174 | CCTCCACGAGGAAGT[C/T]GAAGAGGCGGGCATA | 4542 |
rs139221094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8546632 | CCTAGATAGCTGGGA[C/T]TATAGGTGTGAGTGA | 4542 |
rs139308074 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MYO1F | GRCh38.p7 | 19:8555559 | CACTTGGTGCTCTCC[C/T]GGCCCATTCCTCCCT | 4542 |
rs139317228 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | MYO1F | GRCh38.p7 | 19:8543129 | GGCTGGTCTTGAACT[C/G]CTGACCTCAGGTGAT | 4542 |
rs139400871 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | MYO1F | GRCh38.p7 | 19:8534165 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTAAA | 4542 |
rs139500979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8538751 | CACTACTATGCTTGG[C/T]TAATTTTTAATTTAT | 4542 |
rs139516079 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MYO1F | GRCh38.p7 | 19:8576341 | GTCTCTCAGACTAAC[A/G]CCACCTCTGCCTCTT | 4542 |
rs139595801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8572548 | GCTGGGATTACAGGT[A/G]TGAGCCACTGTGCCC | 4542 |
rs139638434 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | MYO1F | GRCh38.p7 | 19:8522062 | GAGTCTCGCTCTATC[A/G]CCCAGGCTGGAGTGT | 4542 |
rs139728555 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8562516 | AAGAGCTCAACACTT[C/T]GTTTATTTTAAAAAT | 4542 |
rs139742204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8525668 | CCCCGCCCCCTCAGG[A/C]TCTCCCATTAGCACC | 4542 |
rs139851854 | in-del | -/C | 0.0737376 | 0.17729 | intron-variant | MYO1F | GRCh38.p7 | 19:8562163 | CCCGGCTAATTTTTT[-/C]TTTTTTTTTTTGTAT | 4542 |
rs139854706 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8535804 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 4542 |
rs139899049 | in-del | -/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8541425 | TGTGTGTGTGTGTGT[-/G]TTTTTTTTTTTTTTT | 4542 |
rs139911601 | snp | A/C/T | 0.0126979 | 0.078662 | intron-variant | MYO1F | GRCh38.p7 | 19:8522311 | ACAGGCGTGAGCCAC[A/C/T]GCGCCCGGCCGATGT | 4542 |
rs139941279 | snp | C/T | 0.126564 | 0.217402 | intron-variant | MYO1F | GRCh38.p7 | 19:8546891 | ACCATGTTGGCCAGG[C/T]TGGTCTCAAACTCCT | 4542 |
rs139973071 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8545534 | GCTGGAAGTCCTGAG[C/T]GTAGGGTAGAGAAGG | 4542 |
rs139983042 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8564732 | GAGGGAGAGAGGCTG[G/T]GGGGGAGAAGTGGGG | 4542 |
rs140177744 | in-del | -/TT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561471 | CTCCCTCTCTCTCTC[-/TT]TCTTTTTCTCTTTCT | 4542 |
rs140193362 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8540566 | AATACAAAAATTAGC[A/G]GGGCATGATGGTGGG | 4542 |
rs140209365 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8557549 | CTGAATGGATTATCT[A/G]TCTCAGTCCCCCAAA | 4542 |
rs140344606 | in-del | -/CCT | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8557898 | GGCCCCTTCCTTCTC[-/CCT]CCTACCTCTCCTCTT | 4542 |
rs140344714 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8568528 | TAGTCGAGAATTTTG[C/G]CATGTGATGGATTGG | 4542 |
rs140378548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8572615 | AAATTCCTTTTGACT[C/T]CCAGCCTTTCCTGTC | 4542 |
rs140424626 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | MYO1F | GRCh38.p7 | 19:8538823 | TTTGTTGTCACATTC[A/G]TAGCAACAGAATGGT | 4542 |
rs140428641 | in-del | -/A/AG | 0.0366735 | 0.130358 | intron-variant | MYO1F | GRCh38.p7 | 19:8537074 | GGCAGAAGTGAAGAC[-/A/AG]GGGTGGGTGGGGGGC | 4542 |
rs140431962 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | MYO1F | GRCh38.p7 | 19:8535909 | GATGGTCTCGATCTC[C/T]TGGCCTTGTGATCCG | 4542 |
rs140471719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8545964 | ACCCCAGCTCCCTCG[C/T]TTCTCCGCTCTATGA | 4542 |
rs140543028 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | MYO1F | GRCh38.p7 | 19:8570392 | TTTTTTTATTTGAGA[A/T]GGAGTCTCGCTCTTG | 4542 |
rs140565033 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | MYO1F | GRCh38.p7 | 19:8548598 | CTCTATTTTCTTTTT[C/T]TTTTTTTCTTTTTTT | 4542 |
rs140689024 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | MYO1F | GRCh38.p7 | 19:8542518 | TGCTACCAAAGGTTA[C/G]GGCCCTCTGTAGTTC | 4542 |
rs140720485 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | MYO1F | GRCh38.p7 | 19:8523275 | CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC | 4542 |
rs140756462 | snp | A/G | 0.000665834 | 0.0182339 | intron-variant | MYO1F | GRCh38.p7 | 19:8550707 | ACTCTGTGGTACAAC[A/G]GGGGCAGAAACTGTG | 4542 |
rs140769387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8539009 | TTATTAGATAGGCTG[A/G]GTACAGTGGCTCACG | 4542 |
rs140776818 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8527038 | TAGGGAAGGGTCAGC[-/T]AAGGGCCAAGTCAGC | 4542 |
rs140781856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8529164 | GAGGGTGTCCAGGCC[A/C]TATGAGACTATCCAT | 4542 |
rs140786705 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543675 | GTGGTGGTGGTGGTG[C/G]TGGTGGTGGTGGTGG | 4542 |
rs140798554 | snp | A/G | 0.499998 | 0.000998401 | intron-variant | MYO1F | GRCh38.p7 | 19:8560494 | TGGTCTTAAAAAAAG[A/G]AAAAAAAAAAAAGAA | 4542 |
rs140843881 | in-del | -/AGAAAGAAAG | 0.165527 | 0.235296 | intron-variant | MYO1F | GRCh38.p7 | 19:8556497 | AAAAGAAAGAAAGAA[-/AGAAAGAAAG]AGAAAGAAAGAGAAA | 4542 |
rs140868192 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | MYO1F | GRCh38.p7 | 19:8565989 | TGGTATGCGCCTGTA[C/G]TCCCAGCCACTCAGG | 4542 |
rs140951629 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574627 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 4542 |
rs141168772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8546554 | TTGTAGAGATGAGGT[C/T]TCACTATGTTGTCCA | 4542 |
rs141188240 | in-del | -/GGGGGTG | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559331 | ACGGAATGTTCTTGA[-/GGGGGTG]GGGGGTGGGGGGTGG | 4542 |
rs141193771 | in-del | -/AG | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534331 | TCTTTTCTTTTTTTC[-/AG]AGTCTCACTTTGTCC | 4542 |
rs141195985 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8568659 | GCGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4542 |
rs141235240 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8534772 | CTGGGATTACAGGTG[C/T]GCACCACCACACTTG | 4542 |
rs141246249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8539362 | GAGGTTGTGGTGAGC[C/T]GAGATCACGCCATTG | 4542 |
rs141282202 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MYO1F | GRCh38.p7 | 19:8549854 | CACCCAGGCTGGAGT[A/G]CAATAGCGCAATCAT | 4542 |
rs141412651 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | MYO1F | GRCh38.p7 | 19:8528196 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCAAG | 4542 |
rs141452501 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8540274 | GCCTGGAACTCCTGG[C/G]CTCAAGCCAATGTGT | 4542 |
rs141648818 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | MYO1F | GRCh38.p7 | 19:8575828 | CCTTGGGGAGGGGTT[A/G]CCTTTCTTTCAAGTA | 4542 |
rs141649251 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521299 | TGACACACACAGAAA[C/T]GGAGAATGGGCAGCA | 4542 |
rs141658386 | snp | A/G | 0.0667028 | 0.170006 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578391 | TGATCCTCCCAACTC[A/G]GCCTCCCAAAGTGCT | 4542 |
rs141730791 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | MYO1F | GRCh38.p7 | 19:8555000 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTTGTC | 4542 |
rs141749665 | snp | C/T | 0.00694211 | 0.0585052 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521489 | AGGCCGGCAGGCAGA[C/T]AGGCGGGCGAAAGAG | 4542 |
rs141793513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8532715 | ACATAGAAAGACCCC[A/G]TCTCTACAAAAACTA | 4542 |
rs141838083 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8559767 | CCAGCCTGACCAACA[G/T]GGTGAAACTCCATCT | 4542 |
rs141996403 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MYO1F | GRCh38.p7 | 19:8562295 | CATGAGCCACCGCAC[C/T]GGCCCTTCCTTTCTT | 4542 |
rs142090633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8541843 | AGATGGAGTGGGGCC[C/T]GGTCCTCCCTCCATC | 4542 |
rs142197097 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8545583 | ACCCTTGGCCCTCCC[C/G]CTCATCTTCCAGACT | 4542 |
rs142214811 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520450 | AGGCGCCCGCCACCA[C/T]GCCCGGCTACTTTTT | 4542 |
rs142283542 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577820 | TGAGTCCAGGAGTTT[C/G]AGACCAGCCTGGGCT | 4542 |
rs142396793 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | MYO1F | GRCh38.p7 | 19:8546157 | GCAACCTCCGCCTCC[C/T]GAGTTCAAGCGATTC | 4542 |
rs142413652 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | MYO1F | GRCh38.p7 | 19:8523254 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 4542 |
rs142434219 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | MYO1F | GRCh38.p7 | 19:8568126 | ATGCTCCAGCCACCT[A/G]TAAAATCACAGGCTG | 4542 |
rs142542540 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8572371 | CTCTCGGGTTCAAGC[C/G]ATTCTGCTGCCTCAG | 4542 |
rs142569263 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578890 | ATATGCAGCGCCCCT[A/G]GTGGCCACAGCTGGG | 4542 |
rs142617748 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | MYO1F | GRCh38.p7 | 19:8542687 | CTCACTGCAACCTCC[A/G]CCTTCCGGGATCAAG | 4542 |
rs142693483 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539489 | TAATCCCAGCTACTT[A/G]GGAGGCTGAGGCAGA | 4542 |
rs142799836 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | MYO1F | GRCh38.p7 | 19:8561748 | TTGAGATGGAGTCTC[A/G]CTCTGTTGGCCAGGC | 4542 |
rs142817836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8529941 | ATGGAACAGATGGAT[C/G]TAGGCTGGGGGATAG | 4542 |
rs142841757 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8558650 | CTCTGCAAAGGAGTA[A/G]TCTGACAGATAGGAG | 4542 |
rs142922901 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8562598 | TGGAGTGCAGTGGTG[G/T]AATCATAGCTAACTG | 4542 |
rs143014041 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8531324 | TGCACTCCAGCCTGG[G/T]CAACAAGAGCAAAAC | 4542 |
rs143108385 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | MYO1F | GRCh38.p7 | 19:8555069 | GCATGCCTGTAATCC[C/T]GGCTACTTGGGAGGC | 4542 |
rs143208152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8570093 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCTTGCTCT | 4542 |
rs143288207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8544218 | CTTTCCAGCCTGGGT[G/T]CTGGAGGGTGGGGGC | 4542 |
rs143314025 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | MYO1F | GRCh38.p7 | 19:8572771 | GGCCATCACAGCTCA[C/T]TGCAGCCTGGAACTC | 4542 |
rs143326184 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8546224 | TATGTGCCACCACGC[C/T]GGACTAATTTTGTAT | 4542 |
rs143347435 | snp | A/G | 0.0202061 | 0.0984621 | intron-variant | MYO1F | GRCh38.p7 | 19:8530584 | AAAAGCTGGGCGGGG[A/G]TCGTGGGGGGCAAGG | 4542 |
rs143354982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8572563 | GTGAGCCACTGTGCC[C/T]GTGCCCAGTTAGTGG | 4542 |
rs143376679 | in-del | -/GAAC | | | intron-variant | MYO1F | GRCh38.p7 | 19:8555407 | AAAAAAAAAAAAAAA[-/GAAC]AAACAGGGTTGGATC | 4542 |
rs143395564 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8574523 | TTCCTTTATTTCTTC[G/T]TTTTTCCCTTTCTTT | 4542 |
rs143456474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8528613 | TCAGATGGGAATGTG[C/T]TGGTTGGTTGGTTGG | 4542 |
rs143512862 | in-del | -/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574166 | AACATTAAACACCAA[-/C]CCGCCACCACCACCA | 4542 |
rs143542176 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MYO1F | GRCh38.p7 | 19:8565358 | GACCAGCCTGACCAA[C/T]GTGGGGAAACCCCGT | 4542 |
rs143662273 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8558224 | GCTGGAGTGCAGTGG[C/T]GGGATCATAGCTCAC | 4542 |
rs143733196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8542898 | GTGAGCCACTGCACC[C/T]GGCCCTGTTTGCTTT | 4542 |
rs143778203 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8556659 | TTGGGAGGCCAAGAC[A/G]GGTGGATCACCTGAG | 4542 |
rs143814920 | snp | A/G | 0.191775 | 0.243125 | intron-variant | MYO1F | GRCh38.p7 | 19:8560312 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 4542 |
rs143840733 | in-del | -/C | 0.447421 | 0.153379 | intron-variant | MYO1F | GRCh38.p7 | 19:8561594 | CTTCCCTCCCTCCCT[-/C]CTCTTCTCTTTTTTC | 4542 |
rs143854654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8541274 | TTGGGACCTCCAGTG[A/G]TCCTTCTGGCTAGGG | 4542 |
rs143969087 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8573898 | CATCAACAACCACAC[A/G]TAACCAACTACCATT | 4542 |
rs143983212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8575370 | GTGAGCCACCGCACC[C/T]GGCCGGGCATTAGAT | 4542 |
rs143985271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8540583 | GGCATGATGGTGGGC[A/G]TCTATAATCCCAGCT | 4542 |
rs144051400 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | MYO1F | GRCh38.p7 | 19:8573203 | GTAGTCCCAGCTACT[C/G/T]GGGAGGCTGAGGCAG | 4542 |
rs144085544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8576964 | AGACGAGAGACTGGG[C/T]TGGACTGGGAAAGGG | 4542 |
rs144104013 | snp | G/T | 0.111224 | 0.207945 | intron-variant | MYO1F | GRCh38.p7 | 19:8545321 | CTCGAACTCCTGACC[G/T]CAGGTGATCCGCCCA | 4542 |
rs144169495 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574615 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 4542 |
rs144179441 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | MYO1F | GRCh38.p7 | 19:8577124 | ACCACCTACAGATGG[C/G]AGCTTGCTCCCTGGT | 4542 |
rs144179469 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8540007 | ATCCAGCTTCTCGGG[A/G]AAGAGCATCCGGAGG | 4542 |
rs144215111 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8562120 | GCTCACTGCAAGCCT[C/G]GCCTCCAGGGTTCAC | 4542 |
rs144216220 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8571913 | CTGTATTTTTAGAGA[C/T]GGGGTTTCACTGTGT | 4542 |
rs144236868 | snp | C/T | 0.00140779 | 0.0264936 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8530431 | TCCTTGTGCCCCCAC[C/T]CCGCGCCGTTTACCC | 4542 |
rs144322212 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8567355 | CAGGCATGAGCCACC[A/G]TGCCCGGCCCACTGG | 4542 |
rs144348484 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MYO1F | GRCh38.p7 | 19:8564187 | GGAGTTCGAGACCAG[C/T]CTGGCCAACATGGTG | 4542 |
rs144396997 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | MYO1F | GRCh38.p7 | 19:8528005 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGTTTG | 4542 |
rs144467959 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | MYO1F | GRCh38.p7 | 19:8522168 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 4542 |
rs144550920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8554905 | AAAAACAGGGCTGGC[C/T]GGGCGCGGTGGCTCA | 4542 |
rs144596316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8554114 | ACAGGCGTGCACCAC[C/T]GTGTCCGGCTAATTA | 4542 |
rs144615962 | in-del | -/A | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574062 | ACACCTTTCCTCTCC[-/A]AAATAACAGCAACCA | 4542 |
rs144616317 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | MYO1F | GRCh38.p7 | 19:8557057 | TTGGGAGGCCGAGGC[A/G]GGAGGACTGCTTAAG | 4542 |
rs144683390 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559272 | CACGTGGGCAACTGT[A/G]AGGCAGAAGTGGAGC | 4542 |
rs144867079 | snp | A/C/G | 0.0685596 | 0.171987 | intron-variant | MYO1F | GRCh38.p7 | 19:8563712 | AGATGGGCTTTCACT[A/C/G]TGTTGGTCAGGCTGG | 4542 |
rs144925962 | in-del | -/TTTA | 0.0707826 | 0.174302 | intron-variant | MYO1F | GRCh38.p7 | 19:8540339 | TTCATTTTATCTTAT[-/TTTA]TTTATTTATTTATTT | 4542 |
rs144976209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8568877 | AGTGAGCCAAGATTA[C/T]GTCATTGCACTCCAG | 4542 |
rs145008229 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8542694 | CAACCTCCGCCTTCC[A/G]GGATCAAGTGATTCT | 4542 |
rs145063430 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8541173 | ATTATTATTATTTTT[G/T]CTGGCAGAGTAGACA | 4542 |
rs145242446 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | MYO1F | GRCh38.p7 | 19:8556439 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGGC | 4542 |
rs145269171 | snp | G/T | 0.00288629 | 0.0378789 | synonymous-codon | MYO1F | GRCh38.p7 | 19:8522465 | TAGGGCCCGGCACCT[G/T]GGACCATGTGTCCGA | 4542 |
rs145346891 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | MYO1F | GRCh38.p7 | 19:8522317 | GTGAGCCACCGCGCC[C/T]GGCCGATGTCAGGGT | 4542 |
rs145378255 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8525730 | CACTAATTGGCCTCG[C/T]CCCCCAAGGGCCCAA | 4542 |
rs145390661 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | MYO1F | GRCh38.p7 | 19:8542882 | TGCTGGGATTATAGG[C/T]GTGAGCCACTGCACC | 4542 |
rs145403661 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | MYO1F | GRCh38.p7 | 19:8561022 | GATTATAGGTGTGAG[C/T]CACTGCGCCTGGCCA | 4542 |
rs145491530 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578653 | CAGAGCCTGGCCCAG[A/G]TACGTGTCAGCCTAT | 4542 |
rs145614476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8538321 | TTTATCTGAGACAGG[C/G]TCTTGCTCTGTCATC | 4542 |
rs145624058 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | MYO1F | GRCh38.p7 | 19:8556610 | AGCCAATCTGGGGCC[A/G]GGCACAGTGGCTCAT | 4542 |
rs145631384 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8571178 | CTCACCCAGGTCCTG[C/T]GAGCTGTGGTTGCCG | 4542 |
rs145644766 | in-del | -/A | 0.0545821 | 0.155923 | intron-variant | MYO1F | GRCh38.p7 | 19:8538130 | CAGCTCCTTTTTTTT[-/A]TATATATATATTTTT | 4542 |
rs145645587 | in-del | -/TCTT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561469 | CTCTCCCTCTCTCTC[-/TCTT]TCTTTTTCTCTTTCT | 4542 |
rs145650203 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8537324 | CTCACCACTTACCTT[A/G]GCACATAGTAAGTGC | 4542 |
rs145741456 | in-del | -/A | 0.0562307 | 0.157967 | intron-variant | MYO1F | GRCh38.p7 | 19:8564981 | TTCACCACGTTGGAC[-/A]ACGCTCATCTCGAAC | 4542 |
rs145768921 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8574749 | TTTTTCTTTCTTTCT[C/T]TCTCTCTCTCTTTCT | 4542 |
rs145819910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8527621 | GAAGGTGTATGAGTC[A/G]TCTGTTTTGTAGACA | 4542 |
rs145860846 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | MYO1F | GRCh38.p7 | 19:8523285 | TGATCCGCCCGCCTT[A/G]GCCTCCCAAAGTGCT | 4542 |
rs145889532 | in-del | -/AAG | 0.0263992 | 0.111815 | intron-variant | MYO1F | GRCh38.p7 | 19:8532163 | CCATCTCAAAAAAAA[-/AAG]AAAGAAAGAAAAAGA | 4542 |
rs145984163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8549221 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 4542 |
rs146008493 | snp | C/T | 0.163564 | 0.234582 | intron-variant | MYO1F | GRCh38.p7 | 19:8566621 | CTGGCTCAAGCGATT[C/T]TCCTGCCTCAGTTTC | 4542 |
rs146106354 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8537988 | TATTTTTATTTTTAT[C/T]TGGAGACAAAATCTC | 4542 |
rs146125749 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8533611 | ATCCGCCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 4542 |
rs146225868 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521349 | ACCAGGGCCCAGGGG[C/T]GGGGGCTGCAGCAGT | 4542 |
rs146346914 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8566369 | AGATGGGCTTTCACC[A/G]TGTTAGCCAGGATGG | 4542 |
rs146368535 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8562296 | ATGAGCCACCGCACC[A/C/G]GCCCTTCCTTTCTTT | 4542 |
rs146471743 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8548396 | ACTCCTTAGACACAC[A/G]CCTAGCCAACTTCAT | 4542 |
rs146527914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8542583 | ATGGGAGCTCCAGCC[A/G]TTTTTGTTTTTGTTT | 4542 |
rs146542478 | in-del | -/A/AAAA | | | intron-variant | MYO1F | GRCh38.p7 | 19:8547603 | ACGAGACTTTGTCTC[-/A/AAAA]AAAAAAAAAAAAAAA | 4542 |
rs146544943 | in-del | -/T/TCT/TCTTTCT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574654 | TCTTTCCTTTCTTTC[-/T/TCT/TCTTTCT]TCTTTCTTCTTTCTC | 4542 |
rs146554398 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539050 | CAGCACTTTGGGAGG[C/G]TGAGGTGGGCGGATC | 4542 |
rs146711241 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8574534 | CTTCTTTTTTCCCTT[C/T]CTTTCTTTCTTTCTT | 4542 |
rs146733137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8543509 | CTTATCTGAACATAG[A/G]CAGTCTGGTACCCAA | 4542 |
rs146838764 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | MYO1F | GRCh38.p7 | 19:8560521 | AGAACAGGTTCTTGC[C/G]TCTGTCTACACGCAC | 4542 |
rs146947062 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MYO1F | GRCh38.p7 | 19:8534825 | AGAGACGGGGTTTCA[C/T]CATGTTGGTCGGGCT | 4542 |
rs146989990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8532084 | GATTGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 4542 |
rs147079181 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8573117 | ATCGAGACCATCCTT[G/T]CTAACACGGTGAAAC | 4542 |
rs147089372 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | MYO1F | GRCh38.p7 | 19:8538128 | ACCCAGCTCCTTTTT[A/T]TTTATATATATATTT | 4542 |
rs147140635 | in-del | -/AAAC | 0.118933 | 0.212888 | intron-variant | MYO1F | GRCh38.p7 | 19:8557280 | ACTCTGTCTCAAAAA[-/AAAC]AAACAACCAAACAAA | 4542 |
rs147248262 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8550507 | GCTGAGCTAGGAGGA[C/T]GCAGTTCACCCACCC | 4542 |
rs147339116 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | MYO1F | GRCh38.p7 | 19:8540608 | CCAGCTACTCGGGAG[G/T]CTGAGGCAGGAGAAT | 4542 |
rs147345250 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | MYO1F | GRCh38.p7 | 19:8572090 | TGGAGATTGCTGACA[A/G]TCGGTGGCTACCGTC | 4542 |
rs147354904 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8573245 | GAACCTAGGAGGTGG[A/G]GCTTGCAGTGAGCCA | 4542 |
rs147400322 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8530005 | GGGTATACCTGTGAT[A/G]GAACAGATGGATCTA | 4542 |
rs147660247 | snp | G/T | 0.126909 | 0.217598 | intron-variant | MYO1F | GRCh38.p7 | 19:8547598 | GACAGAACGAGACTT[G/T]GTCTCAAAAAAAAAA | 4542 |
rs147691828 | snp | A/C | | | intron-variant | MYO1F | GRCh38.p7 | 19:8540675 | AGATCGTGCCACTGC[A/C]CTCCAGCCTGGGCGG | 4542 |
rs147692861 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578663 | CCCAGGTACGTGTCA[A/G]CCTATGAGCTGGTCT | 4542 |
rs147763540 | snp | C/T | 0.135825 | 0.222405 | intron-variant | MYO1F | GRCh38.p7 | 19:8534660 | AGATGGAGTCTCACT[C/T]TGTTGCCCAGGCTAG | 4542 |
rs147796937 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | MYO1F | GRCh38.p7 | 19:8564829 | CCAGGCTGGAGTGCA[A/G]TGGTATGATTTCGGC | 4542 |
rs147806445 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | MYO1F | GRCh38.p7 | 19:8531842 | TGAAAATGTGGCCGG[A/G]TGCAGTGGCTCAAGC | 4542 |
rs147878935 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | MYO1F | GRCh38.p7 | 19:8522269 | CCTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 4542 |
rs147902198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8548414 | TAGCCAACTTCATGG[A/G]TGATGTCCCCTCATG | 4542 |
rs147912338 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | MYO1F | GRCh38.p7 | 19:8551111 | GGCGGGAGTGCAGCG[G/T]CGCTATCTTGGCTCA | 4542 |
rs148024013 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | MYO1F | GRCh38.p7 | 19:8554925 | GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 4542 |
rs148160806 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MYO1F | GRCh38.p7 | 19:8546353 | ACAGGCATGAGCCAC[C/T]GCACACAGCTTGCTT | 4542 |
rs148274278 | in-del | -/G | 0.21695 | 0.247806 | intron-variant | MYO1F | GRCh38.p7 | 19:8531520 | TGCCCAGCTAATTTT[-/G]TGGTGATGTGGTCTT | 4542 |
rs148281976 | snp | A/C/T | 0.00021765 | 0.0104298 | missense, synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8536967 | TTCTCCTCCCAGTCT[A/C/T]GGGGCCTCTTGGTCT | 4542 |
rs148306444 | snp | C/T | 0.125528 | 0.21681 | intron-variant | MYO1F | GRCh38.p7 | 19:8523300 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG | 4542 |
rs148328349 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8540211 | TTGAGGCAGGGCCTC[A/G]CTTTGTCCTCCAGGT | 4542 |
rs148371835 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | MYO1F | GRCh38.p7 | 19:8575698 | GAAGATTTCAGCATC[C/T]CCAGACAGAGGTGGG | 4542 |
rs148428772 | snp | G/T | 0.0256215 | 0.110247 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521352 | AGGGCCCAGGGGCGG[G/T]GGCTGCAGCAGTGAC | 4542 |
rs148430354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8572120 | CTCAAACATCTCCAC[A/G]CAGAAGCTGGAGCTG | 4542 |
rs148433089 | in-del | -/ACAAAAC | 0.0267878 | 0.112589 | intron-variant | MYO1F | GRCh38.p7 | 19:8555185 | CACTCAGTCTCAAAA[-/ACAAAAC]ACAAAACACAAAAAG | 4542 |
rs148478420 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8547396 | GGATCACGAGGTCAG[A/G]AGTTTGAGACCAGTC | 4542 |
rs148634348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8574379 | AATGGCAGCTACCAT[A/G]GATCAAGTGCATGTT | 4542 |
rs148644054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8541371 | ACTTTAAGGATCCCC[A/G]TCTTATTACTTTACA | 4542 |
rs148681216 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577667 | CAGCTGGCTGCAGGA[C/T]GAACCACCTCTTTTC | 4542 |
rs148781274 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | MYO1F | GRCh38.p7 | 19:8533964 | CTGAGGTGGGCAGAT[C/T]ACTTGAGGTCAGGAG | 4542 |
rs148797423 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8567493 | CCTGCCTCAGCCTCT[G/T]GAGTAGCTGGGATTA | 4542 |
rs148802802 | in-del | -/AGAC | 0.0189856 | 0.0955633 | intron-variant | MYO1F | GRCh38.p7 | 19:8539844 | AGCCCCAGGATTGGT[-/AGAC]AGACAGACGTTGGAA | 4542 |
rs148905101 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8539137 | ATACAAAATTAGGCC[A/G]AGCGCGGTGGCTCAC | 4542 |
rs148947452 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | MYO1F | GRCh38.p7 | 19:8574835 | ATCTCGTCTCATTGC[A/G]ACCTCTGCCTCCTGG | 4542 |
rs149114388 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | MYO1F | GRCh38.p7 | 19:8570063 | AGGTGCATACTACCA[C/T]GCCTGGCTAATACAT | 4542 |
rs149135282 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8572733 | CAGAGTCTGTCTCTG[C/T]TGCTCAGGCTGGAGT | 4542 |
rs149160151 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8523022 | TTAAGCATAATTTTA[A/G]AATTATTTTTTACTT | 4542 |
rs149201095 | in-del | -/AAAC | 0.0248432 | 0.108648 | intron-variant | MYO1F | GRCh38.p7 | 19:8528579 | AAAAACAAAAAAGAA[-/AAAC]AAAAAAGAAACGAGG | 4542 |
rs149264737 | snp | A/C/G | 8.28013e-05 | 0.0064338 | intron-variant | MYO1F | GRCh38.p7 | 19:8554473 | CCCCCAACTCTGTCC[A/C/G]TACCTAATGATGACA | 4542 |
rs149304344 | in-del | -/TGAGGTGC | | | intron-variant | MYO1F | GRCh38.p7 | 19:8552615 | GCAGGTGTAATACTG[-/TGAGGTGC]AAGTCTATGAGATGG | 4542 |
rs149369796 | snp | A/G | 0.0380344 | 0.132554 | intron-variant | MYO1F | GRCh38.p7 | 19:8536650 | GAGTCACCAGTCCTG[A/G]GGGTGGGTGGGAGGT | 4542 |
rs149412658 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MYO1F | GRCh38.p7 | 19:8538154 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 4542 |
rs149476327 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8523809 | ATAGGCACACACCAC[C/T]ATGCCCAGCTAATTT | 4542 |
rs149529709 | snp | C/G/T | 1.65712e-05 | 0.00287843 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8530417 | ACAGCTCCTCCAGGT[C/G/T]CTTGTGCCCCCACCC | 4542 |
rs149618250 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | MYO1F | GRCh38.p7 | 19:8567316 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 4542 |
rs149670241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8534469 | CGTGTCACCATGCCC[A/G]GCTTATTTTGTATTT | 4542 |
rs149786856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8526997 | GACAGGTGAGAGAGA[C/G]AGATGAAGGTGGCTG | 4542 |
rs150189017 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | MYO1F | GRCh38.p7 | 19:8574673 | TTCTTCTTTCTCTCT[C/T]TCTTTCTTTCTTCCT | 4542 |
rs150193994 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8566137 | AACTAGCACTTATTC[C/T]GTGTACCAGGCTCCA | 4542 |
rs150242009 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8579168 | AAGCAAAGGCCCAGA[C/T]ATGGGAAAACCATAG | 4542 |
rs150279394 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8540085 | GACTTTCGGGTACTC[-/T]TCCTCCAGGGGTGGG | 4542 |
rs150291727 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MYO1F | GRCh38.p7 | 19:8523323 | CAGGCATGAGCCACC[A/G]CGCCTGGCCAATTAT | 4542 |
rs150356068 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539167 | CACCTGTAATCCCAG[C/T]GCTTTGGGAGGCTGA | 4542 |
rs150388329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8561878 | CGCACCACCACACCC[A/G]GCTAATTTTTGTATT | 4542 |
rs150397640 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8545970 | GCTCCCTCGCTTCTC[C/T]GCTCTATGAAGCCTC | 4542 |
rs150501039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8575859 | GCAAATCACTTCCTG[C/T]GTTCTTTTGATCAAA | 4542 |
rs150510779 | snp | C/G | 0.014211 | 0.0830875 | intron-variant | MYO1F | GRCh38.p7 | 19:8544291 | GGGTAGGGGCAGGGG[C/G]CGCACCTTGCCAGCG | 4542 |
rs150648046 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | MYO1F | GRCh38.p7 | 19:8559842 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 4542 |
rs150668644 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8571620 | TTTATTGTTTTGAGA[C/T]GGAGTCTTGCTCTCT | 4542 |
rs150709832 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | MYO1F | GRCh38.p7 | 19:8546599 | CCCCAGGCTCAAGCG[A/T]TCCTCTTAACTTAGC | 4542 |
rs150745082 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | MYO1F | GRCh38.p7 | 19:8539024 | GGTACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 4542 |
rs150763373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8549913 | TCAAATGATCCCCCA[A/G]CCTCAGCCCTCTGAG | 4542 |
rs150811028 | in-del | -/T | 0.404733 | 0.196361 | intron-variant | MYO1F | GRCh38.p7 | 19:8546367 | CCGCACACAGCTTGC[-/T]TTTTTTTTTTGAGAC | 4542 |
rs150858195 | in-del | -/CTTT | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574646 | TTCTTTCTTTCTTTC[-/CTTT]CTTTCTCTTTCTTCT | 4542 |
rs150884550 | snp | C/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534332 | CTTTTCTTTTTTTCA[C/G]AGTCTCACTTTGTCC | 4542 |
rs150961153 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8561231 | GGGTGCACCAGTCAG[C/G]GTTAACTGTCTGGGG | 4542 |
rs150965130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8538862 | GGGACTTGGAAAGCA[G/T]ATAGGCAGTGTTTCC | 4542 |
rs151008609 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574623 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 4542 |
rs151077254 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8552320 | CTGGGATTCAGTGGC[A/G]CAATGTCGGCTCACT | 4542 |
rs151131407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8557242 | GTGAGCTGATATTTC[A/G]CCACTACACTCCATC | 4542 |
rs151202130 | in-del | -/GA | 0.0260105 | 0.111035 | intron-variant | MYO1F | GRCh38.p7 | 19:8532105 | CCTGGGCGACAGAGT[-/GA]GACTCAGTCCCCCGA | 4542 |
rs151220096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8545910 | ACATCTGGTTTCAGC[A/C]GTCCTTGACCAATAA | 4542 |
rs151236103 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578370 | CCTTGAACTCCTGAC[C/T]TCAGGTGATCCTCCC | 4542 |
rs151238674 | in-del | -/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8563525 | CTTTCTTTTTTTTTT[-/T]GAGATGGAGTGTCTC | 4542 |
rs151293485 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | MYO1F | GRCh38.p7 | 19:8523268 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 4542 |
rs180683583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8535203 | AGGTGTGAGCCAGTG[C/T]GCCTGGCCAGCAAGA | 4542 |
rs180905554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8548758 | AGGGCCTGCCACCAC[A/G]CCCGGCTAATTTTTT | 4542 |
rs180907585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8567257 | TTTTAGTAGAGATGG[A/G]GGTTTCACCATCTTG | 4542 |
rs180915569 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | MYO1F | GRCh38.p7 | 19:8538579 | GAGCCATTGCTCCCG[G/T]TCTGATTTTTTTTTT | 4542 |
rs180938193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8574322 | ATCGTCACCTCCGTC[A/C]ATCCTCATTGCTGAA | 4542 |
rs180938562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8531762 | ACGAGGTACACTGCC[A/G]TGTCAGAGATGGTAG | 4542 |
rs180965514 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | MYO1F | GRCh38.p7 | 19:8557026 | CGCAATGGCTCACAC[C/T]TGTAATCCCAGCACT | 4542 |
rs180974918 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543720 | GTGCTGGTGGTGGTG[A/G]TGGTGCTGGTGGTGC | 4542 |
rs181137602 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8524330 | CTGAGGCAGGAGAAT[A/C]TCTTGAACCCAGAAG | 4542 |
rs181142816 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8560988 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4542 |
rs181198523 | snp | C/T | 0.000346921 | 0.0131659 | intron-variant | MYO1F | GRCh38.p7 | 19:8553315 | CCATGCAGGTGAGGG[C/T]GACCCAGCTTATCCT | 4542 |
rs181207136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8535400 | AATTAAATTTTACTT[C/T]ATATAGTCTTTGCTG | 4542 |
rs181343658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8539710 | AAATGTATTAGAATA[A/G]TGGTCTACTTCTGCA | 4542 |
rs181354596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8558473 | GCCTGACCCAGACGA[A/C]ACTTTCTTTAGGCCC | 4542 |
rs181359205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8574824 | GCAGTGGCGTGATCT[C/T]GTCTCATTGCGACCT | 4542 |
rs181376532 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | MYO1F | GRCh38.p7 | 19:8523284 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4542 |
rs181578359 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8553935 | TCTCGCTCTCTTTCT[C/G]TCTCTCTGCTCTCAT | 4542 |
rs181596262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8561841 | TCTGCCTCAGCCTCC[C/T]GGGCAGCTGGGACTA | 4542 |
rs181782932 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8574983 | CTGGTCTTGAACTCT[C/T]GACCTCAGGTGATCC | 4542 |
rs181794463 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8544031 | GGCGGTGGCGGTGGC[A/G]GTGGCGGTGCTGGTG | 4542 |
rs181821005 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8559449 | AGCCTTTGGCATAAG[G/T]GTAGATCTGGGTTCT | 4542 |
rs181884689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8531331 | CAGCCTGGGCAACAA[A/G]AGCAAAACTTCATCT | 4542 |
rs182006612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8523311 | GTGCTGGGATTACAG[A/G]CATGAGCCACCGCGC | 4542 |
rs182040172 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8524949 | TGCTTGTTAATCCCA[A/G]CACTTTCGGAGGCCG | 4542 |
rs182043976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8547224 | GAGGATTGCTTGAGC[C/T]CAGGAGGTGTAGACT | 4542 |
rs182064076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8552481 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCAGA | 4542 |
rs182085205 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8569666 | TGGCTGGAAAGTACT[A/G]TGGAGAGGTGAGAGG | 4542 |
rs182203558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8533851 | AAGGCCAACAGGCAG[A/T]TAAAATGTTTGAGGA | 4542 |
rs182215917 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8550826 | TCCTACCCCTTTCAG[C/T]CACTTGCCGCGTGAC | 4542 |
rs182285052 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | MYO1F | GRCh38.p7 | 19:8566482 | TGGTCTATGCTTTTT[A/T]AAAAAAATTTTATTT | 4542 |
rs182288791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8540216 | GCAGGGCCTCGCTTT[A/G]TCCTCCAGGTTGGGG | 4542 |
rs182289752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8562801 | AGTCTCCCAGAGTGC[C/T]AGGATTACAGGCATG | 4542 |
rs182321380 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8525980 | GGTTTCCTCCATGGC[C/T]ACGTCCCTCCTCCAC | 4542 |
rs182493995 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8532163 | TCCATCTCAAAAAAA[A/G]AAAGAAAGAAAAAGA | 4542 |
rs182569847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8563116 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 4542 |
rs182582315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8576457 | TCACTGACTGAATGA[C/T]GAGAAATGAAAGCTG | 4542 |
rs182590905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8544892 | GTGATTCTCCTGCTT[C/T]AGCCTCCTGAGTAGC | 4542 |
rs182599950 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8545368 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGGCAT | 4542 |
rs182601554 | snp | C/G | 0.00123978 | 0.0248667 | missense, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8526902 | GCTGTCGGCGGCATC[C/G]TCTTGGAGGATGAAG | 4542 |
rs182620823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8540839 | TGCTGAAACCCTTAC[A/G]TGCACATGGATCCCT | 4542 |
rs182791385 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | MYO1F | GRCh38.p7 | 19:8560280 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 4542 |
rs182803258 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8555310 | GGGAGGTGGAGGTTG[C/T]AGTGAGCTGAGATTG | 4542 |
rs182803558 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577740 | AAAACCAAGGAAGGG[A/G]CCCAGGGGAGGTGGC | 4542 |
rs182819869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8541467 | AGAATCTCCCTCTGT[C/T]GCCCAGGCTGGAGTG | 4542 |
rs182822856 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8523504 | AGGTATGCTCCACTA[G/T]GCCCAGTTGATTTTT | 4542 |
rs182853755 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8522321 | GCCACCGCGCCCGGC[C/T]GATGTCAGGGTTCTT | 4542 |
rs182856477 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8559928 | GCACTCCAGCCTGGG[A/C]AACAAGAGCAAAACT | 4542 |
rs182868059 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | MYO1F | GRCh38.p7 | 19:8556050 | TTTATTTATTTTGAG[A/T]CAGAGTCTCACTCTG | 4542 |
rs182878028 | snp | C/G/T | 0.0111301 | 0.0738707 | intron-variant | MYO1F | GRCh38.p7 | 19:8523328 | ATGAGCCACCGCGCC[C/G/T]GGCCAATTATTTTTT | 4542 |
rs182939178 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520758 | AGCTGGGATTACAGG[C/G]AGGCACCACCACACC | 4542 |
rs183129893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8572519 | GTGATCCACCTGCCT[C/T]GGCCTCCTAAAGTGC | 4542 |
rs183138947 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8549819 | CAAAAGTTTTTTTTA[A/G]AGACAGGGTCTTGCT | 4542 |
rs183139125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8533456 | GTCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 4542 |
rs183168153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8537495 | CACCCAGGCTGGAGC[A/G]CAATGGTGCCATCTT | 4542 |
rs183194141 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8567605 | CAGGTGATCCTCCCA[C/T]CTCGGCCTCGCAAAG | 4542 |
rs183217821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8532065 | GGTGGTTGCAGTGAG[C/T]GGAGATTGCGCCACT | 4542 |
rs183398956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8571975 | TGATCCGCACGCCTC[A/G]GCCTCCTAAAGTATT | 4542 |
rs183400382 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8529163 | TGAGGGTGTCCAGGC[C/G]ATATGAGACTATCCA | 4542 |
rs183420008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536466 | GCGTTCTGATGAAGG[A/G]GATGGCGAGGGCGGG | 4542 |
rs183426327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8554386 | AGGGCAATGTTCAGA[C/T]TGGGAGTTTCAGGCA | 4542 |
rs183428859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8548898 | CGGCCTTGCACCTCT[A/G]TTTTCTTATCTTTAA | 4542 |
rs183438805 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8545810 | CCCCATGTCCTCTCC[C/T]CTTCTCCATCTCATC | 4542 |
rs183632139 | snp | C/T | | | downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8520425 | CAGCCTCCCGAGCAG[C/T]TGGGACTACAGGCGC | 4542 |
rs183635920 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8524169 | CTCACACCTGTAATC[A/C]CAGCAGTTTGGGAGG | 4542 |
rs183711877 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8528266 | AGGCGCGGTGGCACA[A/C/T]GCCTGTAATCCCAGC | 4542 |
rs183755029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8569718 | TTGCAACATGAACTT[C/T]CCAGGCAGCATCAGT | 4542 |
rs183856570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8529829 | CAGGTGTGTCTGTGC[C/T]GGGTAATGATGTACC | 4542 |
rs183863111 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8546498 | CCGAGTAGCTGGGAC[C/T]GTAGGAGCACACCAC | 4542 |
rs183863302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8566049 | AGGAGTTCGGAGTTA[A/C]AGTGAGCTGTGATTG | 4542 |
rs183949099 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | MYO1F | GRCh38.p7 | 19:8567985 | CCTCCTGGCTCTCCC[A/G]GCTCTGACGACTTGG | 4542 |
rs184040351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8565372 | ACGTGGGGAAACCCC[C/G]TCTCCACTAAAAGTA | 4542 |
rs184089838 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | MYO1F | GRCh38.p7 | 19:8524612 | AAAGAAAGAATTTTT[A/G]GTAGAGACAGGATCT | 4542 |
rs184104278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8561177 | GTGTGAGCCACTGTG[C/G]CTGGCCTGAGAAGGG | 4542 |
rs184176681 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8546284 | GGTCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG | 4542 |
rs184207950 | snp | A/G | 0.00290177 | 0.0379798 | intron-variant | MYO1F | GRCh38.p7 | 19:8521626 | GAGAGAGGAAAGCTT[A/G]AGGTGCCCCTAGCTG | 4542 |
rs184345029 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578328 | ATTTTTAGTAGAGAC[A/G]GAATTTCGCCATGTT | 4542 |
rs184467778 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8560532 | TTGCCTCTGTCTACA[C/T]GCACAGGAGGCTGGG | 4542 |
rs184512203 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8556190 | CCCACCACCATGCCC[A/G]GCTAATTTTTAATAT | 4542 |
rs184517225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8572872 | GGCTAACTTTTAAAT[A/G]CTTTGTAGAGATGGG | 4542 |
rs184540632 | snp | A/G | 1.70246e-05 | 0.00291754 | missense | MYO1F | GRCh38.p7 | 19:8522467 | GGGCCCGGCACCTGG[A/G]ACCATGTGTCCGAGG | 4542 |
rs184546910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8537833 | CTCCTGTGCTCAAGC[A/G]ATCAACTGCCTTAGC | 4542 |
rs184591213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8557447 | GCTGGGACTACAGAC[A/G]TGCACCACCATGCCT | 4542 |
rs184610367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8523239 | GGAGTTTCATCATGT[C/T]AGCCAGGATGGTCTC | 4542 |
rs184717640 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | MYO1F | GRCh38.p7 | 19:8538714 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACCACA | 4542 |
rs184730011 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574442 | TTTGGCACCAGAGAC[C/T]GGTTTAATGGAAGAC | 4542 |
rs184748543 | snp | C/T | 0.00610888 | 0.0549283 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8552111 | CAAGAAGTTGGAGAT[C/T]TTGCCCCCATCTGGC | 4542 |
rs184750480 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8569536 | AACACACTTCCTGGG[C/T]CCCTACTGTGCATGG | 4542 |
rs184782256 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534872 | CCTCGTGATCCACTC[A/G]CCTCGGCTTCCCAAA | 4542 |
rs184782257 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577964 | AACCTGGGAGGTGGA[A/G]GCCTCAGTGAGCCCT | 4542 |
rs184876243 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8569009 | CAAAGAGAAAAAATG[C/T]GCCGAGATGCCTCAG | 4542 |
rs184905160 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8534028 | TATTAAAAACACAAA[A/G]ATTAGCCTGGTGTGG | 4542 |
rs185021865 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MYO1F | GRCh38.p7 | 19:8556835 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCATTG | 4542 |
rs185023976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8573695 | TCTCCACTAAAAGCA[C/T]AAAAATTAGCTGGGT | 4542 |
rs185031196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8551161 | GGTTTAAGCGATTCT[C/T]CTGCCTCAGCCTCCC | 4542 |
rs185158286 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8547104 | GGAGTTCAAGACCAA[C/T]CTGGGCAACAAAGTG | 4542 |
rs185237646 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | MYO1F | GRCh38.p7 | 19:8566374 | GGCTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 4542 |
rs185264493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8530712 | ATTTTTTTAAGAGGC[A/G]GGGTCTTTCTAGTGA | 4542 |
rs185265529 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8552622 | GTAATACTGAAGTCT[A/G]TGAGATGGATATTAA | 4542 |
rs185270138 | snp | C/G | 0.00190078 | 0.0307697 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8526413 | TCTTAACCAGCCTCG[C/G]TGGCCCCGCCCCCTC | 4542 |
rs185277730 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | MYO1F | GRCh38.p7 | 19:8544921 | GCTGGGATTACAGGC[A/G]TGCCGCCACCATGCC | 4542 |
rs185419369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8560359 | GTGTGGGGGTGCGCG[C/G]CTGTAATCCCAGCTA | 4542 |
rs185454769 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8524040 | AGGAGAATTGCTTCA[A/G]CCTGGGAGGTGGAGG | 4542 |
rs185509910 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | MYO1F | GRCh38.p7 | 19:8548809 | GTTTCACTGTGGTCT[C/T]GATCTCCTGACCTCG | 4542 |
rs185514510 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | MYO1F | GRCh38.p7 | 19:8567266 | AGATGGGGGTTTCAC[A/C/T]ATCTTGGCCAGGCTG | 4542 |
rs185545214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8531839 | ATATGAAAATGTGGC[C/T]GGGTGCAGTGGCTCA | 4542 |
rs185545870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8541643 | CATGTTGCCCAGGCT[A/G]GTCTCAAACTCTTGG | 4542 |
rs185757013 | snp | A/G | 0 | 0 | intron-variant | MYO1F | GRCh38.p7 | 19:8545417 | TCTAACTGTGAGCTG[A/G]GGTTCCCGGGGAAAT | 4542 |
rs185758761 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8563336 | ACAGTCTTGCTCTAT[C/T]GCCCAGGCTGGAGTG | 4542 |
rs185795273 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8544037 | GGCGGTGGCGGTGGC[A/G]GTGCTGGTGGTGGTG | 4542 |
rs185797819 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8574828 | TGGCGTGATCTCGTC[C/T]CATTGCGACCTCTGC | 4542 |
rs185820623 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8539791 | CCAGAGCTGGAGGAA[G/T]ACCCTGCTGAACAGA | 4542 |
rs185826671 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8523288 | TCCGCCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 4542 |
rs185830149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8523117 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 4542 |
rs185830859 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8558667 | CTGACAGATAGGAGT[C/G]ATGGCAACTTGGAGC | 4542 |
rs186010157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8563015 | TTTTTGTTTTGATAC[C/T]GAGTCTCACTCTGTC | 4542 |
rs186062890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | MYO1F | GRCh38.p7 | 19:8536019 | GCTCAGTCTCTCTCA[A/G]TCTCTTACTTTCAGT | 4542 |
rs186074494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8535309 | TTACCACTAAGCATC[G/T]GCCATCGTGAATTTC | 4542 |
rs186077369 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | MYO1F | GRCh38.p7 | 19:8554100 | AGTAGCTGGGGACTA[C/T]AGGCGTGCACCACCG | 4542 |
rs186083162 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | MYO1F | GRCh38.p7 | 19:8571559 | AGCTGGGACTACAGG[C/T]GCCCGCCACCGCGCC | 4542 |
rs186103433 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | MYO1F | GRCh38.p7 | 19:8521177 | CACGCTTGTTAAGGA[A/C]CCCCCCCTCCCCAAC | 4542 |
rs186313399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8575560 | TCATGGTTTCTAACA[A/G]ACAGACCATGGCCCG | 4542 |
rs186456451 | snp | G/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8535441 | TTTTTCTTTTTTCTT[G/T]TTGTCTTTTGTAGAG | 4542 |
rs186468116 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8570531 | GCCACCACACCTGGC[A/T]AATTTTTGTGTTTTT | 4542 |
rs186530109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8547536 | TTGAACTCTGGAGGC[A/G]GAGGTTGCAGTGAGC | 4542 |
rs186531833 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | MYO1F | GRCh38.p7 | 19:8531740 | ACACTGTTACTCGAC[A/C]CTATCCACGAGGTAC | 4542 |
rs186571556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8572002 | TATTGGGATTACAGG[C/T]GTAAGCCACCGCGCC | 4542 |
rs186574857 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8546297 | TCGAACTCCCAACCT[A/C]AGGACATCTGCCCAC | 4542 |
rs186578639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8529323 | TGTACCTGGCCCGCC[C/T]AGGTACAGGTGACGG | 4542 |
rs186589960 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8565398 | AAGTACAACATTAGC[C/T]AGGTGTGGTGGCGAG | 4542 |
rs186649365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | MYO1F | GRCh38.p7 | 19:8553729 | ATACAAAAATTAGCC[A/G]GACATGGTGGTGGGC | 4542 |
rs186686150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8549432 | CCAGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 4542 |
rs186789321 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8568517 | TGTGGGGAGGATAGT[C/T]GAGAATTTTGGCATG | 4542 |
rs186819415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8551031 | GATTACAGGCGTGAG[A/C]GTCGTGTCCGGACTG | 4542 |
rs186902889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8567627 | CTCGCAAAGTGCTGG[C/G]ATTATAGGCGTGAGC | 4542 |
rs186934753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8532674 | GGAGCATTGTTGAGC[C/T]CAGGAGTTCAAGACC | 4542 |
rs186987643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8523331 | AGCCACCGCGCCTGG[C/T]CAATTATTTTTTACT | 4542 |
rs187004609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8525428 | AGGTCTGGCTTAGGC[A/C]ATGGGACCCACAACA | 4542 |
rs187022158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8562069 | AGATGGAGTCTTGCT[C/T]TGTCGCCCAGGCTGA | 4542 |
rs187225042 | snp | A/G | 0.00128294 | 0.0252947 | synonymous-codon | MYO1F | GRCh38.p7 | 19:8522423 | GTTGAAGCTCAGCTC[A/G]TCCACATCTTGGCCC | 4542 |
rs187227196 | snp | C/T | 1.69347e-05 | 0.00290982 | intron-variant | MYO1F | GRCh38.p7 | 19:8544269 | GTCTGCGAGGAGGCA[C/T]AGGGTAGGGTAGGGG | 4542 |
rs187261172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8527651 | AGGGTCTCACTCTGT[C/T]GCTCAGGCTGGAGTG | 4542 |
rs187303140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8566876 | AGATAGAGTCTCGCT[A/G]TGTTGCCTAGGCTGG | 4542 |
rs187309177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8540604 | AATCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA | 4542 |
rs187424652 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561375 | CCCTCCCTCCCTCCC[C/T]CCCTTCCCCCCTTCT | 4542 |
rs187445902 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MYO1F | GRCh38.p7 | 19:8560310 | TAACATGGTGAAACC[C/T]CATCTCTACTAAAAA | 4542 |
rs187447067 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8577793 | TTGGGGGGCCAAGGT[C/T]GGAGGATCGCTTGAG | 4542 |
rs187470067 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | MYO1F | GRCh38.p7 | 19:8541585 | AGGTGCGCGCCACCA[C/T]GCCTAGGTAATTTTT | 4542 |
rs187471712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8523600 | AAGCAATCCTCCCAC[G/T]TCGGCCTCCCAACAT | 4542 |
rs187544741 | snp | A/G | 0.00304527 | 0.038902 | intron-variant | MYO1F | GRCh38.p7 | 19:8521629 | AGAGGAAAGCTTGAG[A/G]TGCCCCTAGCTGGCC | 4542 |
rs187556951 | snp | A/G | 0.000215273 | 0.0103726 | intron-variant | MYO1F | GRCh38.p7 | 19:8554464 | GTCTGTGGCCCCCCA[A/G]CTCTGTCCATACCTA | 4542 |
rs187562391 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | MYO1F | GRCh38.p7 | 19:8523312 | TGCTGGGATTACAGG[C/T]ATGAGCCACCGCGCC | 4542 |
rs187570050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8559506 | CTGTGAGTCTCCATC[A/G]TCTCATCTATAAAAA | 4542 |
rs187642105 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | MYO1F | GRCh38.p7 | 19:8556352 | TTTTTAATTAAAAAA[A/T]TTTTTAATGCCAAGT | 4542 |
rs187659034 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | MYO1F | GRCh38.p7 | 19:8573165 | AATAGAAAAAAATTA[C/G]CCAGGCATGGTGGCG | 4542 |
rs187667984 | snp | C/G/T | 0.00041461 | 0.0143926 | synonymous-codon, missense | MYO1F | GRCh38.p7 | 19:8522483 | ACCATGTGTCCGAGG[C/G/T]TGGGGCTTGGGTCGG | 4542 |
rs187674497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8538004 | TGGAGACAAAATCTC[A/G]CTCTGTTGCCAGGCT | 4542 |
rs187760822 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | MYO1F | GRCh38.p7 | 19:8533872 | TGTTTGAGGATGGCC[C/T]AAACCATGTTCATAA | 4542 |
rs187761189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8560076 | CAGTGTGGGTAGGCT[C/T]GAAGGGAAACGGAGG | 4542 |
rs187824097 | snp | A/G | 0.000500394 | 0.0158097 | synonymous-codon, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8550319 | CTCCTGCAGTCGCCC[A/G]CTGTCAATGCCCAGC | 4542 |
rs187828432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8568240 | TATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 4542 |
rs188017021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8572564 | TGAGCCACTGTGCCC[A/G]TGCCCAGTTAGTGGT | 4542 |
rs188048315 | snp | C/G/T | 0.0148955 | 0.0850128 | utr-variant-5-prime, nc-transcript-variant | MYO1F | GRCh38.p7 | 19:8577417 | GGCCCTGCTTCTGCC[C/G/T]GTTCACCGGACTCCC | 4542 |
rs188053696 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8537653 | TGGTCAGGCTGGTCA[G/T]GAACTCCTGACCTCA | 4542 |
rs188088545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8541242 | GTCTTGCTATGTTGC[C/T]CAGGCTGGTCTTAAA | 4542 |
rs188151158 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8567205 | TCGAGTAGCTGGGAT[C/T]ATAGGCACCCACCAC | 4542 |
rs188180684 | snp | A/C/T | 8.35434e-05 | 0.00646263 | intron-variant | MYO1F | GRCh38.p7 | 19:8548321 | ACGGTTGATGGCCTG[A/C/T]GGTGTGGGTGGGGAC | 4542 |
rs188302868 | snp | A/G | | | intron-variant | MYO1F | GRCh38.p7 | 19:8543738 | GTGCTGGTGGTGCTG[A/G]TGGTGCTGGTGGTGG | 4542 |
rs188330846 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | MYO1F | GRCh38.p7 | 19:8556121 | GCAACATCCACCTCC[C/T]GGGTTCAAGCGATTC | 4542 |
rs188342443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | MYO1F | GRCh38.p7 | 19:8524186 | AGCAGTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 4542 |
rs188419292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8569845 | ATAGACAGCCCAGGC[C/G]ATGTGGGGTCAGCAC | 4542 |
rs188567616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8565176 | TGCTGGGAGTACAGG[C/T]GTGAGCCACCACGCC | 4542 |
rs188587233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8523240 | GAGTTTCATCATGTT[A/G]GCCAGGATGGTCTCG | 4542 |
rs188589240 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | MYO1F | GRCh38.p7 | 19:8566234 | GTGCAGTGGCATGAT[C/T]TCGGCTCACTGCAAG | 4542 |
rs188591207 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | MYO1F | GRCh38.p7 | 19:8546585 | GGCTGGCTTTGAACC[A/C]CCAGGCTCAAGCGAT | 4542 |
rs188595692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8528381 | AAAATACAAAAAACT[A/G]GCTGGGCGTGGTGGC | 4542 |
rs188810871 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8542080 | GCCCAGGTGGTCAAG[C/G]CTTTCCTGGGGCCTG | 4542 |
rs188824021 | snp | A/G | | | upstream-variant-2KB | MYO1F | GRCh38.p7 | 19:8578036 | CCTGTCTCTAAAAAC[A/G]AACCAGAAAAAACAA | 4542 |
rs188828837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | MYO1F | GRCh38.p7 | 19:8524936 | GCGCCGTAGCTCATG[C/G]TTGTTAATCCCAGCA | 4542 |
rs188839233 | snp | C/T | | | intron-variant | MYO1F | GRCh38.p7 | 19:8561447 | CTCCCTCCCTTCCTT[C/T]CTCCCTCTCTCCCTC | 4542 |
rs188843833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | MYO1F | GRCh38.p7 | 19:8545981 | TCTCCGCTCTATGAA[A/G]CCTCCTCGAGTCCCA | 4542 |
rs189056782 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | MYO1F | GRCh38.p7 | 19:8556848 | GCCGAGATTGTGCCA[C/T]TGCACTCCAGCCTTG | 4542 |