SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2690 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50826683 | tcttttaaatatctg[G/T]ggggatttgtaCAGA | 11124 |
rs718257 | snp | C/T | 0.287085 | 0.247234 | intron-variant | FAF1 | GRCh38.p7 | 1:50445485 | TCATCCAACTTCTTT[C/T]TCTATATAGAAACTA | 11124 |
rs946499 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50793704 | CTTTAGGAAGACAAT[A/G]AAGGTATTAGTCTAC | 11124 |
rs956084 | snp | A/G | 0.067446 | 0.170804 | intron-variant | FAF1 | GRCh38.p7 | 1:50445675 | TTGTTGATTTAGAGA[A/G]TCGATAATTCAGTAA | 11124 |
rs967584 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576857 | tttttgtagagatgg[G/T]gatctcaccatgttg | 11124 |
rs1015085 | snp | G/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50794996 | TATCTATGTTATTAA[G/T]ATCCTTTTTTTAAAT | 11124 |
rs1149790 | snp | A/T | 0.180342 | 0.2401 | intron-variant | FAF1 | GRCh38.p7 | 1:50491837 | TTTTCAAAAAAAAGT[A/T]ATATGTCAAAAAATA | 11124 |
rs1149791 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | FAF1 | GRCh38.p7 | 1:50498368 | tatgctttcaatgac[C/G]tactaaagaaatcat | 11124 |
rs1149792 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50499817 | acagctaattgacca[A/C]aaccagtaacaaatt | 11124 |
rs1149793 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50502634 | GGCTGCTGACATATA[C/G]GGCAAGTCCAGCCTC | 11124 |
rs1149794 | snp | A/T | 0.190205 | 0.242744 | intron-variant | FAF1 | GRCh38.p7 | 1:50503319 | AACAATATCTATACA[A/T]ttttttatggaaatg | 11124 |
rs1149795 | snp | C/T | 0.203267 | 0.245593 | intron-variant | FAF1 | GRCh38.p7 | 1:50506892 | CAAGAACATTTACCT[C/T]GCAAAGGCTATTGAC | 11124 |
rs1149796 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50513971 | AAGGATTGTATTTGC[A/G]CTGTTTGGAAGGAAG | 11124 |
rs1278636 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50541569 | TTTTTGACATCTTTT[A/G]TTTTTGAGGTTGCCA | 11124 |
rs1278637 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50536719 | TAGATTATATAGCTT[A/G]TAAGTAATGGAATTA | 11124 |
rs1278638 | snp | G/T | 0.471004 | 0.116864 | intron-variant | FAF1 | GRCh38.p7 | 1:50554388 | ATATATATATATATA[G/T]ATAGAGAGAGAGAGA | 11124 |
rs1278748 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50886806 | aggttggttccaagt[C/T]tttgctattgtgaat | 11124 |
rs1315085 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | FAF1 | GRCh38.p7 | 1:50891092 | ctaaacttcccttct[C/T]gcttaatttcattca | 11124 |
rs1315086 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50891732 | aagtttcgtctcaga[A/G]aggtacccagccgtg | 11124 |
rs1334414 | snp | C/T | 0.0177876 | 0.0926144 | intron-variant | FAF1 | GRCh38.p7 | 1:50694448 | AAAAAAATCAGGAAT[C/T]TTACTAATTATCTCA | 11124 |
rs1334415 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50705237 | TCTCTTTTGAAACAG[C/T]GGCCCTGGTTGGTCG | 11124 |
rs1398868 | snp | A/G | 0.36021 | 0.224397 | intron-variant | FAF1 | GRCh38.p7 | 1:50853674 | AAAGATATCTGACAT[A/G]TACTTGATAACCCAA | 11124 |
rs1416685 | snp | C/G | 0.473909 | 0.111197 | intron-variant | FAF1 | GRCh38.p7 | 1:50777702 | CAGCCTGTTATGAGG[C/G]CTAAATTCAAAATGA | 11124 |
rs1464081 | snp | C/T | 0.198634 | 0.244666 | intron-variant | FAF1 | GRCh38.p7 | 1:50869422 | AGCACTAAAAGCCAC[C/T]AGAGAATGGGATGAT | 11124 |
rs1474784 | snp | C/G | 0.271432 | 0.24908 | intron-variant | FAF1 | GRCh38.p7 | 1:50478962 | ATATCTGTAAAACTA[C/G]AACTCTGATCAAGTA | 11124 |
rs1499441 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50560903 | AGCTAAGAATCCACA[A/G]CTCAGCCTGGAGGGC | 11124 |
rs1513640 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | FAF1 | GRCh38.p7 | 1:50778104 | TAGAATTCTACATAG[C/T]AATTAGAATGAATGA | 11124 |
rs1573011 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50904015 | taacaattccacttc[C/T]gggtatatattccaa | 11124 |
rs1573012 | snp | C/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50904319 | gagtagtcaaattca[C/T]agagacagaaagtag | 11124 |
rs1683175 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50816249 | ccattgcactccagc[C/T]tgagcaacagagaga | 11124 |
rs1846522 | snp | A/G | 0.210301 | 0.246828 | intron-variant | FAF1 | GRCh38.p7 | 1:50515533 | TAGTTTGAAAAGCAC[A/G]GTAGTTCAGACAGCA | 11124 |
rs1849553 | snp | C/T | 0.280256 | 0.248162 | intron-variant | FAF1 | GRCh38.p7 | 1:50852333 | AGGTCTGTTCTTTCT[C/T]TATTGTTTGGATATT | 11124 |
rs1935301 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50902045 | AAATAATGAACTTCC[A/G]AAGAAAGTAACTTTT | 11124 |
rs1972100 | snp | A/G | 0.401215 | 0.199083 | intron-variant | FAF1 | GRCh38.p7 | 1:50819789 | TATACATATATATAC[A/G]TATATATATATACAT | 11124 |
rs2048636 | snp | C/G | 0.471578 | 0.115772 | intron-variant | FAF1 | GRCh38.p7 | 1:50848346 | CTTCATTTAACAGCC[C/G]TAtacggcattgtat | 11124 |
rs2090013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758345 | AGGCATAAGCCACCA[C/T]GCCCAGCACAACATA | 11124 |
rs2095864 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50833925 | AAACCACATTACTCT[C/T]TTAACTGGTCTCTCT | 11124 |
rs2095865 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50834015 | ATGTCAAATTGTAAT[C/T]CACAATGTTAGAGGA | 11124 |
rs2102038 | snp | A/C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50526393 | gtgcaggctggtctt[A/C/G]aactcctgggctcaa | 11124 |
rs2105211 | snp | C/G | 0.212728 | 0.247206 | intron-variant | FAF1 | GRCh38.p7 | 1:50834138 | GGGTGTAGCACCCCC[C/G]CTTCGCCCTCTTCCT | 11124 |
rs2137676 | snp | C/G | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50752167 | tagagacgggggtct[C/G]gtcctgttggccagg | 11124 |
rs2153765 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50937163 | ATATGTGTCAAAATT[G/T]TAAGGTATTACTATT | 11124 |
rs2173547 | snp | A/T | 0.105569 | 0.204058 | intron-variant | FAF1 | GRCh38.p7 | 1:50556856 | Cataaaataaaataa[A/T]ataaaataaaataaa | 11124 |
rs2175794 | snp | A/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50867507 | CCCTAGCCCAGTTTT[A/T]AATAGGATTGTTTGT | 11124 |
rs2207075 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50519884 | GGCCTAACTCTGCTA[A/G]GCAGCTCTAACACCC | 11124 |
rs2221933 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50737673 | TTCTTAACCCAAAAC[A/C]AACTATTAACAGACC | 11124 |
rs2404720 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | FAF1 | GRCh38.p7 | 1:50870435 | gcactcccgcctggg[C/T]gacagggcaagactc | 11124 |
rs2405004 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50948459 | caacccagactatca[C/T]atggcaagagaggga | 11124 |
rs2405008 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50957895 | ACAATTTTGTAACAC[A/G]GTAAAACTACACCTT | 11124 |
rs2644544 | snp | A/G | 0.0259275 | 0.110867 | intron-variant | FAF1 | GRCh38.p7 | 1:50898641 | AGTTTTTTGTGGTCT[A/G]TCCTGGAGAATGCCC | 11124 |
rs2781796 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | FAF1 | GRCh38.p7 | 1:50731463 | caagctctgcctccc[A/G]ggttcacgccattct | 11124 |
rs2781797 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731495 | ctgcctcagactccc[A/C]agtagctgggactac | 11124 |
rs2781798 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731623 | tccgcctgccttggc[A/C]tcccaaagtgctggg | 11124 |
rs2781799 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731659 | aggcatgagccaccg[C/T]gcctggctCATAACA | 11124 |
rs2781800 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731671 | accgtgcctggctCA[A/T]AACACTTGTCTTCTA | 11124 |
rs2789899 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885194 | ttttttgaaaagata[A/G]acaatattgacaaat | 11124 |
rs2789900 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746294 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 11124 |
rs2896886 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50613967 | ccgggcgtggtggca[C/T]gtgcctgtaatctca | 11124 |
rs2896887 | snp | C/T | 0.281313 | 0.248031 | intron-variant | FAF1 | GRCh38.p7 | 1:50677721 | ccaacatggagaaac[C/T]ctgtctctactaaaa | 11124 |
rs3033415 | in-del | -/TTTATTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50557930 | ttatttatttattta[-/TTTATTT]gatacagggtcttgc | 11124 |
rs3033489 | in-del | -/AT/TA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694001 | atgtcaagtatatat[-/AT/TA]aatgacacatataca | 11124 |
rs3062915 | in-del | -/ACACACAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819669 | cacacacacacacac[-/ACACACAC]TCTCTCTCTGtatat | 11124 |
rs3062918 | in-del | -/TA/TACG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819739 | atatacatatatata[-/TA/TACG]catatatatatacat | 11124 |
rs3062921 | in-del | -/AT/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819740 | tatacatatatatac[-/AT/GT]atatatatatacata | 11124 |
rs3747997 | snp | C/T | 0.199564 | 0.24486 | intron-variant | FAF1 | GRCh38.p7 | 1:50846947 | ATATATAAGAGTGTA[C/T]TGCAGGTGCTGTTTG | 11124 |
rs3789575 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FAF1 | GRCh38.p7 | 1:50472280 | CCACTGATGTACATA[C/T]GGCTCTAACATGTCC | 11124 |
rs3789576 | snp | G/T | 0.145978 | 0.227331 | intron-variant | FAF1 | GRCh38.p7 | 1:50479854 | ATGAAGAGATACGAG[G/T]TAAATCAGCAACCTT | 11124 |
rs3789577 | snp | A/G | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50488456 | GCCAGTATGGTTGAC[A/G]ATACACTAATACACA | 11124 |
rs3789578 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50516640 | TTCTTGACAAAAGAC[C/T]AAGAAGCAAATGCAA | 11124 |
rs3789579 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50531251 | CCGAGCTATTGTTCA[C/G]ATACAAGTTAATCAG | 11124 |
rs3789580 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50550469 | GGCATCTTAGTCACT[C/G]ATCAAAGCTTTCAAG | 11124 |
rs3789581 | snp | C/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50553778 | GATAAAAGGTTATAA[C/T]GCTATAGAGAAGTTA | 11124 |
rs3789582 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50561719 | TAGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 11124 |
rs3789583 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50562561 | AAGAGTAAAGTTCTA[A/G]CTTCATCTTTATGTG | 11124 |
rs3789584 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | FAF1 | GRCh38.p7 | 1:50563715 | ACAAAATGAATAAGC[C/T]CTTCAGGAGATCACA | 11124 |
rs3789585 | snp | C/G | 0.16911 | 0.236552 | intron-variant | FAF1 | GRCh38.p7 | 1:50585433 | TTTACTACCTGCTGA[C/G]CACTGATGAATATGC | 11124 |
rs3789586 | snp | C/T | 0.332106 | 0.236133 | intron-variant | FAF1 | GRCh38.p7 | 1:50588650 | CTGAGTCTTGTCAGC[C/T]TAGACAGTTAAGAGT | 11124 |
rs3789587 | snp | C/T | 0.211819 | 0.247067 | intron-variant | FAF1 | GRCh38.p7 | 1:50800802 | TCTGCTGTTTCTGTT[C/T]GCCTCATCCGCACTT | 11124 |
rs3789588 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50800851 | GACTTAGAAATCCCA[A/G]CCACCAAAATTCAAG | 11124 |
rs3827730 | snp | C/T | 0.468949 | 0.12067 | intron-variant | FAF1 | GRCh38.p7 | 1:50472176 | ACAGGAGTTGGCCTA[C/T]AGGAGGAGTAGTGGG | 11124 |
rs3827731 | snp | A/G | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50522155 | ATAATATTTGCGAAT[A/G]TGGCAATGTCTCATC | 11124 |
rs3838294 | in-del | -/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50588598 | TGGTGTGTGTGTGTG[-/TG]GTGACTTGAGGTCTA | 11124 |
rs3838295 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50858094 | TATGTAATTTAAATT[-/T]CAAATAGGTATATGA | 11124 |
rs3850873 | snp | A/G | 0.477937 | 0.102688 | intron-variant | FAF1 | GRCh38.p7 | 1:50597304 | GCCCACTGTCACCTT[A/G]TATTCTGGGGTCTTT | 11124 |
rs3850874 | snp | C/T | 0.492087 | 0.0623997 | intron-variant | FAF1 | GRCh38.p7 | 1:50597459 | ATATAAAAAAATGCC[C/T]ATAGAATTTGAATAA | 11124 |
rs3862271 | snp | C/T | 0.305685 | 0.24372 | intron-variant | FAF1 | GRCh38.p7 | 1:50489324 | ACTGAGAGTAATAAC[C/T]AACAGAGTTTTCCTC | 11124 |
rs3888843 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469950 | TTAAAGGTACTACTG[C/T]TGAGCTTGTTCCATT | 11124 |
rs3900170 | snp | A/G | 0.0102772 | 0.0709436 | intron-variant | FAF1 | GRCh38.p7 | 1:50492784 | CTCAGCATTCTCTTA[A/G]GTGAGATAGCTAATC | 11124 |
rs3900215 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50496119 | TGAATTAGTCTTTTA[A/G]GAGTTAACTGATGAT | 11124 |
rs3992056 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50698210 | NNTCATCCTAAGAAA[A/G]AAATGTAACCAACCT | 11124 |
rs4256860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50685543 | TTAAATACTACTTAC[C/T]TATCTTCTGCATCAG | 11124 |
rs4275494 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50924704 | aaaagatacataggc[C/T]aggcacagtggctca | 11124 |
rs4285749 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50794344 | AAATTACACTGCTGT[A/G]GTACTACGACCACAA | 11124 |
rs4381241 | snp | C/T | 0.491473 | 0.0647364 | intron-variant | FAF1 | GRCh38.p7 | 1:50441766 | GTGGAGGTACCTTTC[C/T]TGCACAGCTCAGCCT | 11124 |
rs4448562 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50523415 | atttgtgtctacatc[C/T]tcataaattcttatg | 11124 |
rs4454589 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50847911 | cacacacacacccct[C/T]taggcatatcatatt | 11124 |
rs4477329 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50675505 | CAGACTAGCTGATTG[C/T]TGTTATAGAAAATGT | 11124 |
rs4492667 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50943724 | CCTCATTTTAGAGAG[A/C]TCTACACAGTTATCT | 11124 |
rs4926554 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50456969 | GACTATGTAAACTTG[A/G]ACCAGCCATTTCTGC | 11124 |
rs4926555 | snp | A/G | 0.492966 | 0.0588865 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468158 | gggctgcagtgagct[A/G]taattgtgtcactgc | 11124 |