SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11027 | snp | C/T | 0.452103 | 0.147154 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176509515 | AGTTGTAGATTGAGC[C/T]GAATAACCATGGGAA | 23197 |
rs11320 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176509873 | AAACCAGTTGTAGAG[C/T]GGAGCTCCTTGTTCA | 23197 |
rs12341 | snp | A/G | 0.237014 | 0.249662 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176508734 | ATCTGACTGCTGTCA[A/G]TAAAATGTATCTGGC | 23197 |
rs753379 | snp | C/G | 0.330016 | 0.236849 | intron-variant | FAF2 | GRCh38.p7 | 5:176493119 | ATGGGAATGCTGTGG[C/G]AATAGGCAAAAGGGG | 23197 |
rs754350 | snp | A/C | 0.496175 | 0.0435625 | intron-variant | FAF2 | GRCh38.p7 | 5:176493440 | TGTGCGTGCTCCTGC[A/C]TGTGCGTGCTCCTGA | 23197 |
rs754351 | snp | C/T | 0.49621 | 0.0433651 | intron-variant | FAF2 | GRCh38.p7 | 5:176493289 | TTGCCTGGCATACAG[C/T]AGGTGCTCAGTTTTT | 23197 |
rs1049975 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176507025 | AACAACAGCAAGTCA[A/G]AAAAAAAAAACAAGA | 23197 |
rs1991473 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAF2 | GRCh38.p7 | 5:176505010 | CCTGGGCGACAGAGC[A/G]AGACCTGTCTGGGAA | 23197 |
rs2033198 | snp | A/G | 0.264906 | 0.249555 | intron-variant | FAF2 | GRCh38.p7 | 5:176466062 | ATACTTACAGTATCT[A/G]TTTTATTACACGGTA | 23197 |
rs2115050 | snp | C/T | 0.263535 | 0.249633 | intron-variant | FAF2 | GRCh38.p7 | 5:176462256 | CAGAATCTCACTCTG[C/T]CACCCAGGCTGGAGT | 23197 |
rs2115051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF2 | GRCh38.p7 | 5:176462190 | CTCTTGGGTTCAAGC[A/G]ATTCTCCCGCCTCAG | 23197 |
rs2162764 | snp | C/T | 0.263535 | 0.249633 | intron-variant | FAF2 | GRCh38.p7 | 5:176462015 | tgttgggactacagg[C/T]gtgagacactgcacc | 23197 |
rs2162777 | snp | C/T | 0.247621 | 0.249989 | intron-variant | FAF2 | GRCh38.p7 | 5:176502101 | GAGATAATGTGGATG[C/T]GCCTCACACAGTATC | 23197 |
rs2277068 | snp | A/G | 0.47023 | 0.118317 | intron-variant | FAF2 | GRCh38.p7 | 5:176489248 | GGTTTTTGCAAACAA[A/G]AGGTAAGACTAATTT | 23197 |
rs2277069 | snp | C/G/T | 0.00015415 | 0.00877806 | intron-variant | FAF2 | GRCh38.p7 | 5:176489066 | TTTCAGCTCCAAAGT[C/G/T]TTACTATTCTACTAA | 23197 |
rs2335415 | snp | G/T | 0.345037 | 0.231231 | intron-variant | FAF2 | GRCh38.p7 | 5:176466575 | TAGCTGTTTGAGCCA[G/T]CTGGTTAAAATACTA | 23197 |
rs2335803 | snp | C/T | 0.495056 | 0.049474 | intron-variant | FAF2 | GRCh38.p7 | 5:176458639 | tcaaactcctgacct[C/T]gtgatctgcccacct | 23197 |
rs2434376 | snp | A/G | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176492023 | TGGTTCAAAAGCCAT[A/G]AAGCAGCAAGTGTTA | 23197 |
rs2434415 | snp | A/C | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176489981 | TAACAAGAGCTCATC[A/C]TTGGAAGCTACAGAG | 23197 |
rs2913727 | snp | A/T | 0.468148 | 0.122112 | intron-variant | FAF2 | GRCh38.p7 | 5:176474391 | CAACAGGAACTACAC[A/T]TAAGCACTGTTCTCT | 23197 |
rs2913728 | snp | A/T | 0.26518 | 0.249539 | intron-variant | FAF2 | GRCh38.p7 | 5:176473114 | aatcagaataaagaa[A/T]ggacttttgttaata | 23197 |
rs2913729 | snp | A/G | 0.495745 | 0.0459295 | intron-variant | FAF2 | GRCh38.p7 | 5:176487584 | ACTTTCTGTGTCTGT[A/G]GCCAGGAAGCTCTGG | 23197 |
rs2913730 | snp | A/C | 0.494976 | 0.0498674 | intron-variant | FAF2 | GRCh38.p7 | 5:176466941 | TTTCTCCCACTGATA[A/C]TATCAGGCAATTACA | 23197 |
rs2913731 | snp | C/G | 0.495291 | 0.0482933 | intron-variant | FAF2 | GRCh38.p7 | 5:176470219 | AAACCAGTTGTATTA[C/G]TAATGGTTGGAACCA | 23197 |
rs2913736 | snp | A/C | | | intron-variant | FAF2 | GRCh38.p7 | 5:176454631 | ATGTTGCTAACTTCC[A/C]ACAAGCATGTATTAT | 23197 |
rs2913738 | snp | A/T | 0.466308 | 0.125343 | intron-variant | FAF2 | GRCh38.p7 | 5:176452261 | CAAGGTTTCCCCGTG[A/T]TGGCCAGGCTGGTCT | 23197 |
rs2913745 | snp | A/G | 0.25214 | 0.249991 | intron-variant | FAF2 | GRCh38.p7 | 5:176481610 | tgcagtgagctgaga[A/G]catgccactgcactc | 23197 |
rs2913895 | snp | C/G | 0.250168 | 0.25 | intron-variant | FAF2 | GRCh38.p7 | 5:176490857 | GAAAAAAAAATAAAG[C/G]CTTTAAGAGAGAATT | 23197 |
rs2913896 | snp | C/T | 0.470715 | 0.117409 | intron-variant | FAF2 | GRCh38.p7 | 5:176494460 | GGGTCATATTACCTT[C/T]GCTTTATGGTTTAGG | 23197 |
rs2913897 | snp | A/G | 0.49621 | 0.0433651 | intron-variant | FAF2 | GRCh38.p7 | 5:176494782 | AAACTCCTGGACTCA[A/G]GTGAGCAGCCCACCT | 23197 |
rs2913898 | snp | C/T | 0.251014 | 0.249998 | intron-variant | FAF2 | GRCh38.p7 | 5:176478302 | GGGAATATAGAGAGA[C/T]CCCGTCTTTACAAAA | 23197 |
rs2913899 | snp | C/T | 0.298398 | 0.245271 | intron-variant | FAF2 | GRCh38.p7 | 5:176478430 | ACTGCAGTGAGCAGT[C/T]ATTGCGCTATTGCAC | 23197 |
rs2913900 | snp | A/T | 0.229723 | 0.249176 | intron-variant | FAF2 | GRCh38.p7 | 5:176497366 | TAAGATCACTGATAA[A/T]CCTACCACCACTTGA | 23197 |
rs2913901 | snp | C/G | 0.247621 | 0.249989 | intron-variant | FAF2 | GRCh38.p7 | 5:176499745 | CCTGCTGTGGCCTCT[C/G]AAGTAGCTGGAACTA | 23197 |
rs2913902 | snp | A/G | 0.495855 | 0.045338 | intron-variant | FAF2 | GRCh38.p7 | 5:176503487 | ttgaacctgggaggc[A/G]gaggttgcagtgaat | 23197 |
rs2913903 | snp | C/G | 0.247905 | 0.249991 | intron-variant | FAF2 | GRCh38.p7 | 5:176504228 | cgcctctaatcccag[C/G]actttgggaggccga | 23197 |
rs2913904 | snp | C/T | 0.255224 | 0.249945 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176508728 | ATCACCATCTGACTG[C/T]TGTCAATAAAATGTA | 23197 |
rs2913915 | snp | A/C | 0.462253 | 0.132093 | intron-variant | FAF2 | GRCh38.p7 | 5:176482790 | caaagtgttgggatt[A/C]cagacgtgagccacc | 23197 |
rs2963296 | snp | C/T | 0.255224 | 0.249945 | intron-variant | FAF2 | GRCh38.p7 | 5:176504769 | CATGAATGGATTAGA[C/T]AAGAGGAACATGGAT | 23197 |
rs2963297 | snp | A/G | 0.0368353 | 0.130617 | downstream-variant-500B | FAF2 | GRCh38.p7 | 5:176510546 | AGTTGGTTCCAACAA[A/G]AGTGACAAATTCCTT | 23197 |
rs2963301 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | FAF2 | GRCh38.p7 | 5:176502346 | tgatccgcctgcctc[A/G]gcctcccaaagtgct | 23197 |
rs2963657 | snp | G/T | 0.259951 | 0.249802 | intron-variant | FAF2 | GRCh38.p7 | 5:176452469 | AGGTGGTATGCATAA[G/T]GAAGCAGATCTATTG | 23197 |
rs2963658 | snp | C/T | 0.343924 | 0.231686 | intron-variant | FAF2 | GRCh38.p7 | 5:176454695 | TTTATTTCCCCATTC[C/T]AATTCCAGGTTTGTT | 23197 |
rs2963659 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | FAF2 | GRCh38.p7 | 5:176464025 | gtgagccactgtgcc[A/G]ggccTTAAATTTTTC | 23197 |
rs2963660 | snp | A/G | 0.34526 | 0.23114 | intron-variant | FAF2 | GRCh38.p7 | 5:176468022 | atacaaaaattaatc[A/G]ggtgtgttggtgggc | 23197 |
rs2963661 | snp | A/G | 0.26518 | 0.249539 | intron-variant | FAF2 | GRCh38.p7 | 5:176470310 | CAGCCGGGTGCGGTG[A/G]CTCACGCCTATAATC | 23197 |
rs2963663 | snp | C/T | 0.427271 | 0.176281 | intron-variant | FAF2 | GRCh38.p7 | 5:176482640 | CAGCCTCCTGAGTAG[C/T]TAGGACTACAAGCAC | 23197 |
rs2963664 | snp | A/G | | | intron-variant | FAF2 | GRCh38.p7 | 5:176482664 | caagcacacaccacc[A/G]catccagctaatatt | 23197 |
rs2963666 | snp | C/T | 0.277067 | 0.24853 | intron-variant | FAF2 | GRCh38.p7 | 5:176487057 | TTCTTTTTCTTACCC[C/T]TGGGGTTATACTCAC | 23197 |
rs2963667 | snp | C/T | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176488834 | GAAGAAGGAACTGTA[C/T]TTTAGAGGAACAAAT | 23197 |
rs2963668 | snp | C/T | 0.247621 | 0.249989 | intron-variant | FAF2 | GRCh38.p7 | 5:176490077 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 23197 |
rs2963669 | snp | A/G | 0.255503 | 0.249939 | intron-variant | FAF2 | GRCh38.p7 | 5:176496353 | AGGCGGGGAAAAAGC[A/G]GAGACTAAATGATAC | 23197 |
rs2963670 | snp | A/G | 0.491831 | 0.0633856 | intron-variant | FAF2 | GRCh38.p7 | 5:176496430 | TGTGGAAAGTCTAAG[A/G]GTTGATCTTTTTCAC | 23197 |
rs2963671 | snp | C/T | 0.250631 | 0.251182 | intron-variant | FAF2 | GRCh38.p7 | 5:176497138 | ATGACAGAGCAGGAC[C/T]CTGTCTTTAAAAAAT | 23197 |
rs2963672 | snp | C/T | 0.430583 | 0.172886 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176508315 | TATTCCAAAGTGTTC[C/T]GTAGCTAGACTGGTG | 23197 |
rs2963673 | snp | A/G | 0.254664 | 0.249956 | downstream-variant-500B | FAF2 | GRCh38.p7 | 5:176510372 | ACTTGAATTTCCCCA[A/G]CTATAAATGAAGATA | 23197 |
rs2963674 | snp | A/G | 0.247053 | 0.249983 | downstream-variant-500B | FAF2 | GRCh38.p7 | 5:176510393 | AATGAAGATAATGCC[A/G]TCCACCTCAGGATAG | 23197 |
rs2963677 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | FAF2 | GRCh38.p7 | 5:176506059 | ggagtgcaagcgccc[A/G]ccaccacgcctggct | 23197 |
rs2963678 | snp | C/T | 0.251859 | 0.249993 | intron-variant | FAF2 | GRCh38.p7 | 5:176506024 | ttttcgtatttttag[C/T]agagatggggtttca | 23197 |
rs2963686 | snp | G/T | 0.333261 | 0.235728 | intron-variant | FAF2 | GRCh38.p7 | 5:176477307 | GGCCAGGCTGGTCTC[G/T]AACTCCTGACCTCAT | 23197 |
rs2963687 | snp | G/T | 0.495135 | 0.0490805 | intron-variant | FAF2 | GRCh38.p7 | 5:176480195 | tactgagtggatgtt[G/T]aattttgtcaaaACA | 23197 |
rs3217316 | in-del | -/GTT | 0.220351 | 0.248236 | intron-variant | FAF2 | GRCh38.p7 | 5:176494150 | GTTTATAGTCAGCAA[-/GTT]GTTCTCATATCCTTT | 23197 |
rs3756768 | snp | G/T | 0.330482 | 0.236691 | intron-variant | FAF2 | GRCh38.p7 | 5:176490788 | ACAATCAGCTTTTTT[G/T]ATTTTTTAGAAAAAA | 23197 |
rs3834277 | in-del | -/G | 0.498754 | 0.0249289 | intron-variant | FAF2 | GRCh38.p7 | 5:176490533 | CTCTGCTCCCTAGAG[-/G]CAGGGTAAAGGCTGT | 23197 |
rs3842082 | in-del | -/G | 0.375 | 0.216506 | intron-variant | FAF2 | GRCh38.p7 | 5:176489293 | ATATGGTGGGGGGGG[-/G]AGGGGGAGACAAATA | 23197 |
rs3888233 | snp | C/T | 0.271972 | 0.249033 | intron-variant | FAF2 | GRCh38.p7 | 5:176485993 | CAATGTAGGCAGTAC[C/T]CCTGGAGTTATGCAG | 23197 |
rs4045162 | in-del | -/AC/CA | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176456577 | TCAAGCAGTCCACCC[-/AC/CA]CTTGGCCTCCCAAAG | 23197 |
rs4551090 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | FAF2 | GRCh38.p7 | 5:176462974 | TTCTCTTGAAACAAC[A/G]TTTCTGCTTGAATCT | 23197 |
rs4868640 | snp | A/G | 0.268995 | 0.249277 | intron-variant | FAF2 | GRCh38.p7 | 5:176490998 | GGAACGTTGTTGTCA[A/G]TGAATTTGGTTTGAT | 23197 |
rs4868641 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | FAF2 | GRCh38.p7 | 5:176494712 | ggcatgcaccaccac[A/G]cccagctaatttttt | 23197 |
rs5873535 | in-del | -/T | 0.25634 | 0.24992 | intron-variant | FAF2 | GRCh38.p7 | 5:176486674 | TACAGAAACTACTCA[-/T]TTTTTTTTTCTTTTC | 23197 |
rs5873536 | in-del | -/T | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176486683 | TACTCATTTTTTTTT[-/T]CTTTTCTTTGCCAGT | 23197 |
rs5873537 | in-del | -/A | 0.417845 | 0.185278 | intron-variant | FAF2 | GRCh38.p7 | 5:176503556 | GCAAAATTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23197 |
rs6556271 | snp | C/T | 0.264632 | 0.249571 | intron-variant | FAF2 | GRCh38.p7 | 5:176451450 | ctgctgcctcagagg[C/T]tgagattacagtgtt | 23197 |
rs6866627 | snp | A/G | 0.120674 | 0.21395 | intron-variant | FAF2 | GRCh38.p7 | 5:176456877 | TATGTTGCTGAATCT[A/G]TTCAAGAACATAGTT | 23197 |
rs6871487 | snp | C/T | | | intron-variant | FAF2 | GRCh38.p7 | 5:176468349 | cagcactttgggagg[C/T]cgaggcaggtggatc | 23197 |
rs6889369 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FAF2 | GRCh38.p7 | 5:176453831 | gaggccgaggctggc[A/G]gatcacgaggtcagg | 23197 |
rs7700747 | snp | C/T | 0.465892 | 0.126058 | intron-variant | FAF2 | GRCh38.p7 | 5:176462480 | aataccaaaattagc[C/T]gggcgtggtggcgca | 23197 |
rs7702142 | snp | A/T | 0.249603 | 0.25 | intron-variant | FAF2 | GRCh38.p7 | 5:176491047 | AGTAGAATTGTATAC[A/T]CAGGGGGAATTTGTT | 23197 |
rs7703718 | snp | C/T | 0.0425829 | 0.139564 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176508858 | GTCAGAGCCTTCCTC[C/T]CCATCTGGAATTCAC | 23197 |
rs7704499 | snp | C/G | 0.0333695 | 0.124785 | utr-variant-3-prime | FAF2 | GRCh38.p7 | 5:176509209 | CTGAGACCCTAGGCC[C/G]GTCTCCTTGCTGACC | 23197 |
rs7708363 | snp | A/G | 0.269538 | 0.249235 | intron-variant | FAF2 | GRCh38.p7 | 5:176485330 | tcagtcttcaagtca[A/G]ctgataccaagttgt | 23197 |
rs7708676 | snp | A/G | 0 | 0 | intron-variant | FAF2 | GRCh38.p7 | 5:176479598 | GTTGTCTAGGTAGTC[A/G]TGTTCTCTGCAACTC | 23197 |
rs7708814 | snp | A/G | | | intron-variant | FAF2 | GRCh38.p7 | 5:176451786 | tatacgtgtgtgtgt[A/G]tatatatatatacat | 23197 |
rs7713154 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | FAF2 | GRCh38.p7 | 5:176485754 | ttatttttagagaca[A/G]ggtctcgtttcattg | 23197 |
rs7724162 | snp | C/T | | | intron-variant | FAF2 | GRCh38.p7 | 5:176488166 | tatttttagtagaga[C/T]agggttttaccatgt | 23197 |
rs7724297 | snp | A/G | 0.0252325 | 0.109451 | upstream-variant-2KB | FAF2 | GRCh38.p7 | 5:176447496 | AATctcattcaacaa[A/G]tggcaaaatggagcc | 23197 |
rs7725080 | snp | A/G | 0.0232847 | 0.105357 | upstream-variant-2KB | FAF2 | GRCh38.p7 | 5:176447712 | GTCACGGCGGTGGAC[A/G]GCAAGCTGTGCGGAC | 23197 |
rs7730599 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | FAF2 | GRCh38.p7 | 5:176506543 | ATTAATTCAGAGTAG[G/T]ACTAGTGTTGGGCTT | 23197 |
rs7732877 | snp | A/G | 0.247905 | 0.249991 | intron-variant | FAF2 | GRCh38.p7 | 5:176494935 | AAGCCTGCCACATTC[A/G]TAGAAATACCCAGTC | 23197 |
rs9647576 | snp | A/T | | | intron-variant | FAF2 | GRCh38.p7 | 5:176451894 | tatatatatatatat[A/T]ttttttttttttttt | 23197 |
rs9765363 | snp | A/C | | | intron-variant | FAF2 | GRCh38.p7 | 5:176506211 | aaaaaaaaaaacaaa[A/C]aaaaaaaaCTGGATC | 23197 |
rs10039150 | snp | A/G | 0.120674 | 0.21395 | intron-variant | FAF2 | GRCh38.p7 | 5:176464051 | TTTTCTATTGCTGCT[A/G]CACAAATTAAAATTG | 23197 |
rs10044221 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF2 | GRCh38.p7 | 5:176488332 | GGAAAGAATGAGTGT[A/G]TATCATTTGGGGAAC | 23197 |
rs10050658 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAF2 | GRCh38.p7 | 5:176466212 | ATGATCACTTAATTT[C/T]CTGAACAGATTTCAG | 23197 |
rs10051756 | snp | A/G | 0.291 | 0.258786 | intron-variant | FAF2 | GRCh38.p7 | 5:176451006 | GCCATTAAACAAACA[A/G]TTGTTGAAACTTATT | 23197 |
rs10054778 | snp | C/T | 0.281841 | 0.247964 | intron-variant | FAF2 | GRCh38.p7 | 5:176489082 | ACTTTGGAGCTGAAA[C/T]TTAGGCCAAAATAAG | 23197 |
rs10055062 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | FAF2 | GRCh38.p7 | 5:176468412 | acacggtgaaacccc[A/G]tctctactaaaaata | 23197 |
rs10055450 | snp | C/T | 0.223225 | 0.248562 | intron-variant | FAF2 | GRCh38.p7 | 5:176458407 | ATTTTTCtttttctt[C/T]ctttttttttttttt | 23197 |
rs10063364 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF2 | GRCh38.p7 | 5:176458197 | agccatctttccagc[C/T]ccccttcttgcgtag | 23197 |