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 |