SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs35904030 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50709401 | TTATCAGTATATCCC[-/C]TTGGAAAGTAGCACA | 11124 |
rs35910195 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50858926 | ATCCAACAGCACATC[-/A]AAAAGTAAATTAACC | 11124 |
rs35911050 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50477843 | AATATGCACTTGGAA[-/A]GGGAAGGAATAAACT | 11124 |
rs35934575 | in-del | -/T | 0.253544 | 0.249975 | intron-variant | FAF1 | GRCh38.p7 | 1:50857311 | TAAACTTTTTTTTTT[-/T]AGCATTTCTAAGGCA | 11124 |
rs35936303 | in-del | -/C | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459646 | TCTTCTCTTCATCCC[-/C]AAATTGTTGCCATCT | 11124 |
rs35983172 | in-del | -/A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694567 | GGAAAAAAAAAAAAA[-/A/C]CCCACAAAGGTCTCC | 11124 |
rs35993240 | snp | A/T | 0.470618 | 0.117591 | intron-variant | FAF1 | GRCh38.p7 | 1:50665695 | TGGCCTAAAAAGCCC[A/T]AAATAGGAATTATCT | 11124 |
rs35993642 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50858482 | CTGCTAGACACATGT[-/G]GGCTAGTGAGTCCTT | 11124 |
rs35997260 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50567260 | AAAATCTGATCAATT[-/T]AAAATATCCACTAAT | 11124 |
rs35999034 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50764482 | CCAATCTCAGTCTCA[-/G]GGGAATCTCCTAGCT | 11124 |
rs36000484 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50654376 | TTACTTTTACTTTTT[-/T]AAAAAAACTTAGGTA | 11124 |
rs36004603 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50826761 | GATAGACAAACTCTT[-/AAC]AAAATACAACCTGTG | 11124 |
rs36009998 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885728 | CCATTTTGTTACTTG[-/T]TTTTCCAGTTGTTTT | 11124 |
rs36018827 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50743616 | TATAGGCGTGAGCCA[C/T]TGCGCCCAGCCAAAA | 11124 |
rs36045755 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50500711 | TTGAAAATGATATTG[-/G]AGTGTGCCTATGTTA | 11124 |
rs36051023 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50839379 | GATATGCAAAGAAGT[-/A]CTGGTATTAATAGAC | 11124 |
rs36053491 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836170 | TGTTTTTTGTTTCTG[-/T]TTTTTTTTTTTTTTT | 11124 |
rs36053834 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50621417 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 11124 |
rs36071834 | snp | C/T | 0.3746 | 0.216737 | intron-variant | FAF1 | GRCh38.p7 | 1:50723396 | CAGAGCAAGACTGTC[C/T]CCAAAAAAAAAAAAA | 11124 |
rs36096271 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50923396 | CCAGCCTGGGTGACA[-/G]GGGTAAGACCTTGTG | 11124 |
rs41286821 | snp | A/T | 0.00597247 | 0.0543191 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440844 | AGCAGCAGTAAATAA[A/T]TATCTTGCATATATG | 11124 |
rs41292141 | snp | A/C | 0.0876345 | 0.190099 | intron-variant | FAF1 | GRCh38.p7 | 1:50490958 | AGGACATCCTTTGGT[A/C]TTCCTTTCTGACCTT | 11124 |
rs41292699 | snp | A/G | 0.0110318 | 0.0734453 | intron-variant | FAF1 | GRCh38.p7 | 1:50655572 | AAATAGAATTTTCAC[A/G]TGACTTACAGTTTCC | 11124 |
rs41305632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50633372 | TTCCATCTCCTTGCA[C/T]TTTGAAATCTCCACA | 11124 |
rs41478350 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50683991 | TTTTTTATTTGTTGG[C/T]ATTATAGCATCTATG | 11124 |
rs55637473 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50906469 | ATAAATTATCTTGGG[C/T]AGTATGGCCATTTTC | 11124 |
rs55694728 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | FAF1 | GRCh38.p7 | 1:50549517 | GGGCATGGTGGCTCA[C/T]GACTGTACTCCCAGC | 11124 |
rs55721112 | snp | C/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50705172 | CTAGCTTTTAGGTGG[C/G]TGGGGCCCAAGGCAT | 11124 |
rs55724112 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FAF1 | GRCh38.p7 | 1:50892341 | CCTGCTTTGGTTCAC[A/G]CTTGGTGCGCTGCAC | 11124 |
rs55728484 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649363 | TCCATGTTGGTCAGG[A/C]TGGTCTTGAACTCCT | 11124 |
rs55728524 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457603 | AAGCTTATTTGATTT[C/T]TTGGTCAGGTGTGGT | 11124 |
rs55732047 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50759849 | GATCGTCATTCTAAC[A/T]GGTGTGAGATGGTAA | 11124 |
rs55743332 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50805397 | CCCTCTAAAATGCCA[A/T]CTTCCATAGCACACT | 11124 |
rs55770483 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50818443 | CCAAAGACCAGTATA[A/C]AAATATTCGTACCGG | 11124 |
rs55770916 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50939407 | ACTGGATTTTTGTAC[A/T]CTGATTTTATATCCT | 11124 |
rs55771842 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749934 | AGTGCCTAATACATA[C/T]TAAGGAACTCAAAAA | 11124 |
rs55827769 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510185 | AAAAAAAAAAAAAAA[A/T]TTAAATTTAAAACTC | 11124 |
rs55836912 | in-del | -/CAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50663841 | AATATAATTAATAAT[-/CAT]TTGTTACAGAAATTC | 11124 |
rs55839847 | snp | A/G/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50863178 | TTCTGTCAGACCACA[A/G/T]TAGAATAAAATTGGA | 11124 |
rs55855890 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50892996 | TAAAATGCATTCTTG[A/T]GTAGTTCAATTGCAT | 11124 |
rs55859203 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50791380 | CTACTCTGTGATGCT[A/G]GGGCCAGTATTCTGC | 11124 |
rs55874244 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729525 | AATTCTCATGCCTCA[G/T]CCTCCTGAGTAGCTG | 11124 |
rs55889880 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575094 | TTTGTATTTTTAATA[A/G]AGACGGGGTTTCACC | 11124 |
rs55916309 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50766581 | TGGAGGGAAGGCATT[C/G]AGAGTGGATGAAGGG | 11124 |
rs55922890 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50699728 | TGAGCCTTCCTTTTC[C/T]TTTGAAAACTAAAAA | 11124 |
rs55954520 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50903615 | AAAAATGGCAATAAA[C/T]AGAGGACATCAGGAG | 11124 |
rs55986089 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50955550 | TTCAAAATTTTGGTG[C/G]TGCAGCCACTATAGA | 11124 |
rs56001578 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50648487 | AGTATTTACTCAGAG[C/T]CTGTATGGGAAAACA | 11124 |
rs56014400 | snp | A/T | 0.0337553 | 0.125452 | intron-variant | FAF1 | GRCh38.p7 | 1:50725465 | AGACATTTAAAAAAA[A/T]TTTTTTTTGAGACAG | 11124 |
rs56019576 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749924 | TGTTTTGCAGAGTGC[C/T]TAATACATACTAAGG | 11124 |
rs56028018 | snp | C/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961068 | TGAGACGGAGTCTCG[C/T]ACTGTGGCCCGGGCT | 11124 |
rs56037430 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50725653 | TAAAGAAGGGGTTTC[A/G]CCATGTTGTCCAGGC | 11124 |
rs56057793 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50903369 | CTTATAAATTATAAT[A/G]ATTAGCACACTGTGT | 11124 |
rs56104424 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881597 | TGGGGATTTGAGTAA[A/G]TACTTCCATACATGT | 11124 |
rs56172127 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50905262 | TGGTGTACATGTGCC[A/G]CATTTTCTTAATCCA | 11124 |
rs56201451 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50604327 | TATCAGTGATCCCAC[C/G]ATCCCCAACAGATTC | 11124 |
rs56202902 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50525780 | GTGGATTTTGGCCAA[C/T]TTTTTTTCTGTGTCA | 11124 |
rs56207132 | snp | C/T | 0.124144 | 0.21601 | intron-variant | FAF1 | GRCh38.p7 | 1:50575154 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 11124 |
rs56213411 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50852734 | ATTAGCCCTCAGTTT[C/G]TCATCTATATAATAA | 11124 |
rs56214447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50547038 | GGACTACAGGTAAGC[A/G]CCACCATGCCTGGAT | 11124 |
rs56215652 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50888665 | ATATGCTGGATTACG[C/T]TTACTGATTTGCGTA | 11124 |
rs56229310 | snp | A/T | 0.115438 | 0.210697 | intron-variant | FAF1 | GRCh38.p7 | 1:50703012 | TCAAAAATTAAAAAA[A/T]ATATATATATAAAAT | 11124 |
rs56266143 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50748936 | GCTACAATGCAATTA[C/T]TCATGGTCTCAATGA | 11124 |
rs56268558 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50876627 | GTCTCACTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 11124 |
rs56269966 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50955563 | TGGTGCAGCCACTAT[A/G]GAAAACAATATGACA | 11124 |
rs56272614 | snp | C/T | 0.28052 | 0.24813 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467528 | CCATGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 11124 |
rs56273459 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50515433 | TTATACAGGAAATTT[A/G]TGAAAACACAGACTC | 11124 |
rs56274214 | snp | A/T | 0.276534 | 0.248588 | intron-variant | FAF1 | GRCh38.p7 | 1:50703014 | AAAAATTAAAAAAAA[A/T]ATATATATAAAATAC | 11124 |
rs56298082 | snp | C/T | 0.220246 | 0.248223 | intron-variant | FAF1 | GRCh38.p7 | 1:50484055 | AATCTGGGAGTCAAA[C/T]GTATAGACAATATAA | 11124 |
rs56323917 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50951380 | ACAGAGAACAAGTAC[A/T]TACCTTAAAACTGTC | 11124 |
rs56360209 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50937386 | AAGAGTTAATGCTAA[C/T]ATAGTTGCCTTCATA | 11124 |
rs56393503 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922482 | AAAAAAAAAAAAAAA[-/A]GAAAAGAGAGAGAGA | 11124 |
rs56402443 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50494486 | AGAACAACTGGATTA[C/T]GAGATTCAGAAACAG | 11124 |
rs56719774 | in-del | -/C | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50796060 | AAAACAACAACAACA[-/C]AAAAAAAACAAAAAC | 11124 |
rs56743286 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50471723 | ATCAGTGGACTCTTA[-/A]GAGTTCATCTGCCAT | 11124 |
rs56778303 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | FAF1 | GRCh38.p7 | 1:50624186 | GCAGTCTATCTCTGT[A/C]GCCCAGGCTGGGGTG | 11124 |
rs56789242 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50730984 | TCCTATTGTGTTATA[A/C/T]TGAATTTGCACCTTC | 11124 |
rs56806783 | in-del | -/A | 0.229136 | 0.249128 | intron-variant | FAF1 | GRCh38.p7 | 1:50630057 | GCGAGCCTCTGTCTC[-/A]AAAAAAAAAACATAT | 11124 |
rs56837046 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50796544 | TTTCCTTTGTGCCCA[C/T]TGGTGGTCAGCAGGG | 11124 |
rs56907396 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704734 | ATCAGATCAGAAAAA[-/AA]TTTTAAAGAGTTTAG | 11124 |
rs56908494 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556855 | CATAAAATAAAATAA[-/AA]TATAAAATAAAATAA | 11124 |
rs56985406 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50534023 | CATTTACCCCCTCAG[A/G]ATCCATGTTCTCTAC | 11124 |
rs56997734 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50894698 | AATGGAATAAACCTA[A/G]AAATCAATAATGAGG | 11124 |
rs57016473 | in-del | -/TA | 0.167809 | 0.236103 | intron-variant | FAF1 | GRCh38.p7 | 1:50637914 | GTATATATATATATA[-/TA]CACCAACACATGATC | 11124 |
rs57074997 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | FAF1 | GRCh38.p7 | 1:50505592 | GTTAGTAAACTATGT[A/G]TGGTCTTTGGGCCAA | 11124 |
rs57092469 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50703297 | AACTTTCCAATCATG[C/T]AACAAGAAAAAATGT | 11124 |
rs57095912 | snp | G/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50891158 | TGATGAAATCGGCTA[G/T]TGAAGCTTGTACATG | 11124 |
rs57172783 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847435 | AAAAAAAAAAAAAAA[-/A]CAGTAACAGAGATGA | 11124 |
rs57183177 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50914273 | TTCATCAAATACACC[A/G]AAGAGGAAATTTGGT | 11124 |
rs57223383 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50926528 | GCTGTGGGGTGACAT[A/G]GTTAACTATAATTTA | 11124 |
rs57230400 | in-del | -/TCTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527840 | CTCTCTCTCTCTCTC[-/TCTC]CCTCTCTCCCTCTCT | 11124 |
rs57254915 | snp | G/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50673329 | GAATAATTTCCCAAT[G/T]GATGTATAAGCAACT | 11124 |
rs57281556 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50718535 | TCCTGTTATGTGCAT[-/AT]GTTATTTCTTTTCTT | 11124 |
rs57298510 | in-del | -/GAAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50879287 | AATGAATGAATGAAT[-/GAAT]CAGATTAATGTAATT | 11124 |
rs57342753 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649574 | CAAAGAGCTTTGATT[C/T]TAAAATTCCTAGTTT | 11124 |
rs57362903 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808673 | AAAAAAAAAAAAAAA[-/A]CTTTTCTCCCTAACA | 11124 |
rs57400675 | snp | C/T | 0.114036 | 0.209795 | intron-variant | FAF1 | GRCh38.p7 | 1:50602985 | TAAGGATTATAATCC[C/T]CACTTTAGAGATGAG | 11124 |
rs57412341 | snp | A/G | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50844655 | GATTCGGGAAAAATG[A/G]ATACAAAGAATCTGG | 11124 |
rs57421400 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50772422 | ATTGCAACAGTATTC[A/C]CAATAGCTAAGACAT | 11124 |
rs57446850 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50531665 | AAACCAAATACTACT[A/C]ATGAAAATGTCTAAG | 11124 |
rs57468024 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50570238 | GAGAAGACAAGCGAA[C/T]GCAGACGGTGAAAAA | 11124 |
rs57489116 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50666143 | TCAAAAAAAAAAAAA[-/A]GACCAGGTGATCTGC | 11124 |
rs57490213 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50540120 | TGATTACAAGCTCCC[A/G]CCACCACACCTGGCT | 11124 |
rs57523646 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50929099 | AAAAAGAAAGAAAAG[-/A]AAAAAAAAACTGGGA | 11124 |
rs57528056 | in-del | -/AC/CA | 0.289424 | 0.246872 | intron-variant | FAF1 | GRCh38.p7 | 1:50779992 | ACACACACACACACA[-/AC/CA]GAGGAAGTAAAAGAG | 11124 |
rs57541625 | in-del | -/GTGGAAATACA | 0.625 | 0.125 | intron-variant | FAF1 | GRCh38.p7 | 1:50490547 | TCAGTATCAAATACA[-/GTGGAAATACA]ACCCAGCTTTTGAAT | 11124 |
rs57544709 | in-del | -/CC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527868 | CTCTCTCCCTCTCTC[-/CC]TCTCTCTCTCTCTCT | 11124 |
rs57545230 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50759838 | GACTTTTTAATGATC[A/G]TCATTCTAACTGGTG | 11124 |
rs57607955 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847681 | ATTAATCATGAATTT[-/T]CAAAACCAACTAGAG | 11124 |
rs57609567 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50898581 | TTTACAATGAAAAAA[-/A]TAAAAGATAATTTCT | 11124 |
rs57621664 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575253 | TTTGAACTAATTTAA[A/G]AAATAATTTTAATAT | 11124 |
rs57643686 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748492 | GTGAAACTCTGTCTC[-/AA]AAAAAAAAAAAAAGA | 11124 |
rs57657521 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692325 | TCTAATCTTTTAGCA[A/T]TTTTGAAATATATAA | 11124 |
rs57731439 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733793 | ATGGTACTTTGTTAT[-/T]AGCAGCCCTAGCAAA | 11124 |
rs57743355 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50612079 | AGTATCTTAATAGTT[G/T]GAAAAATTTAAAAAC | 11124 |
rs57773328 | in-del | -/GCT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50849447 | CATTCTAAACACACT[-/GCT]ATCACTCATTATACA | 11124 |
rs57775942 | snp | A/G | 0.225301 | 0.248777 | intron-variant | FAF1 | GRCh38.p7 | 1:50501534 | GGCGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 11124 |
rs57779128 | in-del | -/AAGG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490519 | AGGAAGGAAGGAAGG[-/AAGG]TAGGTTAACAGCTTC | 11124 |
rs57793888 | snp | A/G | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50735752 | ACAGGGTCTTGCTCT[A/G]CTGCCCAGGCTTAAA | 11124 |
rs57839936 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50840601 | TCTAACTATATACTT[C/T]AGATTTATGTATTTC | 11124 |
rs57957311 | snp | A/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50900904 | AGAGGTAAAATCACT[A/T]CCCCAGGTACTGTTA | 11124 |
rs57980948 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50851100 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC | 11124 |
rs58004439 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928749 | AATCACGCCATTGGA[C/T]TCCAGCCCAGGCAAC | 11124 |
rs58029717 | snp | A/G | 0.111576 | 0.20818 | intron-variant | FAF1 | GRCh38.p7 | 1:50696456 | TTAATCAACCCCAAC[A/G]AACATTTGCCTTTGA | 11124 |
rs58190330 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50932796 | ACGAGAGCCCCACCC[C/T]TGCAGCAAACTTTTG | 11124 |
rs58193277 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50662713 | TTTTTTTTTTTTTTT[-/T]GAAACGGAGTCTCCC | 11124 |
rs58215354 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50821129 | ACCACAAGGTTGTTA[G/T]AAGAATCAAATGAAA | 11124 |
rs58235906 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | FAF1 | GRCh38.p7 | 1:50874926 | AGCCATGGACCACCA[C/T]GCCCAGCTAATCTTT | 11124 |
rs58236240 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874905 | CTGTAATGTAGCTGA[A/G]ACTACAGCCATGGAC | 11124 |
rs58241436 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50635589 | TGCCACTATACCCAA[C/T]TAATTTTTGTATTTT | 11124 |
rs58252400 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869629 | CATGTCATCTTTTAA[-/A]TTTTCTATACAAATT | 11124 |
rs58305289 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50728061 | AATAAACTCCCTTGC[A/G]TATATACATATATCC | 11124 |
rs58314543 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50891778 | CCCCTACTGGGGCCT[A/G]CCTCCCAGTTAGGCT | 11124 |
rs58384431 | snp | C/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50759597 | TGCTATTGTGAATAG[C/T]GCCGCAATAAACATA | 11124 |
rs58392694 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543767 | CACTGTTTTTTTTTT[-/T]CCATTCAGAAAATGA | 11124 |
rs58415078 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50766923 | ACAGTGTCTTCTCAC[C/T]TCCACACAACCACAC | 11124 |
rs58418926 | in-del | -/GT/GTGTGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530276 | TGTGTGTGTGTGTGT[-/GT/GTGTGT]ATGTATATATGTATA | 11124 |
rs58432198 | snp | C/T | 0.130008 | 0.219321 | intron-variant | FAF1 | GRCh38.p7 | 1:50790419 | TGCAGGGATTACAGG[C/T]GTGAGCCACCGCACC | 11124 |
rs58446086 | snp | A/G | 0.114738 | 0.210248 | intron-variant | FAF1 | GRCh38.p7 | 1:50506129 | AATGGACAGGTTTCT[A/G]GGTATCTAGGACAAG | 11124 |
rs58504145 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909140 | CACTTATGAAGCTTA[A/G]TTTGGCTGGATATGA | 11124 |
rs58507793 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50542556 | GATAAAAGTGTACCA[G/T]TGCATCCAGTGGCAG | 11124 |
rs58511862 | in-del | -/AAAAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50722664 | AAAAAAAAAAAAAAA[-/AAAAAA]GCCCTATAAAATCTA | 11124 |
rs58544593 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50768894 | GAACTAAAGAAACAA[A/G]AAGAAACCAATTACA | 11124 |
rs58567132 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50753774 | TTTTTTTTTTTTTTT[-/TT]GAGACATAGTCTCGC | 11124 |
rs58573193 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50956208 | GGGAGGATTTTCTTA[A/G]AGGACAATTTGGGGT | 11124 |
rs58574309 | snp | C/T | 0.115088 | 0.210473 | intron-variant | FAF1 | GRCh38.p7 | 1:50494508 | CAGAAACAGGTCTTA[C/T]GTGTTGCCTAGGCTA | 11124 |
rs58672235 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50867771 | TGAAAAACAGCATGG[A/C]GATTCCTTAAAGAAC | 11124 |
rs58686129 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50741991 | TGGGAATAGCAGAAA[C/T]CACCTAGTGAAGAGT | 11124 |
rs58695465 | in-del | -/GGTATCCCTTGC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50518114 | TGTGGTATCCCTTGC[-/GGTATCCCTTGC]AGTCCACGCTTTCCT | 11124 |
rs58762442 | in-del | -/TAA | 0.212728 | 0.247206 | intron-variant | FAF1 | GRCh38.p7 | 1:50944986 | GCAAAACTGGCTTTC[-/TAA]TAAGTAAGGTGTGTG | 11124 |
rs58791125 | snp | A/G | 0.217851 | 0.247924 | intron-variant | FAF1 | GRCh38.p7 | 1:50877184 | GAGAAACCTAACAAC[A/G]CTCAGTCAGGTGATC | 11124 |
rs58795848 | snp | A/G | 0.165853 | 0.235413 | intron-variant | FAF1 | GRCh38.p7 | 1:50817838 | TGAATTCCATGATAC[A/G]TGAATTATATCTCAA | 11124 |
rs58813795 | snp | C/T | 0.161924 | 0.233971 | intron-variant | FAF1 | GRCh38.p7 | 1:50908570 | CCTGTATTGGGTGCA[C/T]ATATATTTAGGATAG | 11124 |
rs58818877 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50674764 | ATCATTCTCTCAATT[C/T]CCCAACATTATCACT | 11124 |
rs58832551 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713791 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 11124 |
rs58895507 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | FAF1 | GRCh38.p7 | 1:50933081 | TCCTCCTGGGCCTCC[A/G]TGCCTATGATGAGAG | 11124 |
rs58902185 | in-del | -/A | 0.480064 | 0.0978296 | intron-variant | FAF1 | GRCh38.p7 | 1:50679323 | AAGTACAAAAAAAAA[-/A]GAATAGCATTTCATT | 11124 |
rs58904547 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50924659 | TACAGCAGAGCTATA[A/G]TAACCAAAACAGCAT | 11124 |
rs58946586 | in-del | -/AAAAAAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50678797 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GGCCAGTCATGGTGG | 11124 |
rs59020486 | snp | C/T | 0.120674 | 0.21395 | intron-variant | FAF1 | GRCh38.p7 | 1:50508342 | AACAATCTGAATGTC[C/T]AGCTACAGATGAATA | 11124 |
rs59029934 | snp | C/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50527084 | CTGGTCTCAAACTCC[C/T]AGCCTCAAGTATCTG | 11124 |
rs59066916 | in-del | -/AAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556857 | TAAAATAAAATAATA[-/AAA]TAAAATAAAATAAAA | 11124 |
rs59078269 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929089 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAA | 11124 |
rs59097691 | snp | C/T | 0.212425 | 0.24716 | intron-variant | FAF1 | GRCh38.p7 | 1:50928426 | TGCTTTTAGTCTCAG[C/T]GGCATTAATTCTTTA | 11124 |
rs59110918 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50896655 | CAACCTTTAAGGACA[C/T]TATGCTAAATGAAAT | 11124 |
rs59114947 | in-del | -/AC | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50796228 | CACACACACACACAC[-/AC]CCCTATCTTCTTGCA | 11124 |
rs59128535 | snp | A/T | 0.212425 | 0.24716 | intron-variant | FAF1 | GRCh38.p7 | 1:50874729 | TGATTTAAGTCTCCA[A/T]CCCTTCTCCATCTTA | 11124 |
rs59136667 | snp | G/T | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50678811 | AAAAAAAAAGGCCAG[G/T]CATGGTGGCTCACGC | 11124 |
rs59137959 | in-del | -/AAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50827635 | ATCAATAAATACTAA[-/AAAA]TAAATAAATAAATAA | 11124 |
rs59160200 | in-del | -/GT/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820848 | TGTGTGTGTGTGTGT[-/GT/TG]ACACATACCAGATTT | 11124 |
rs59182122 | in-del | -/C | 0.471483 | 0.115954 | intron-variant | FAF1 | GRCh38.p7 | 1:50576634 | CTCATCTCCGCACCG[-/C]CCCCCCCCCCGCCAC | 11124 |
rs59187392 | in-del | -/TG | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50692293 | GTGTGTGTGTGTGTG[-/TG]GTGGGAACATTTAAA | 11124 |
rs59218631 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50565601 | CTACTTAACAGACTT[C/T]TTTAGTAAAACATAA | 11124 |
rs59269579 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50886363 | ATATTATTCCAGGGT[C/T]AAAGTTTTTTTCCTT | 11124 |
rs59299964 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50666143 | CAAAAAAAAAAAAAA[-/A]GACCAGGTGATCTGC | 11124 |
rs59318346 | snp | A/C | 0.211819 | 0.247067 | intron-variant | FAF1 | GRCh38.p7 | 1:50725260 | TAGGATCTGAGGCCC[A/C]GTGCAGACTTCCCTA | 11124 |
rs59390962 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50848859 | GAGAGGCTACAGAGA[C/T]GTGAAAACTAAATGT | 11124 |
rs59396661 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830674 | TTTTTTTTTTTTTTT[-/T]ACCAACTCCAATGGC | 11124 |
rs59409846 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836079 | CCTATCTCATCTATT[-/T]CACAAAACAGAAATA | 11124 |
rs59412984 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50546586 | GGTCAGGTTGGTCTC[A/G]AACTCCTGGCCTTGT | 11124 |
rs59430062 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50796992 | AATAAAAAAATTAGC[C/T]GGGCTTGGTGGCACA | 11124 |
rs59431798 | in-del | -/TGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50780680 | CAGAGAGGACTATGA[-/TGA]GCATGTGCTGCCACC | 11124 |
rs59524047 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50933543 | TTGTCAAAGCCATTC[A/G]ACAAGTCTCTAGGAG | 11124 |
rs59542416 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50906579 | GTTTGTAGTTCTCCT[C/T]GAAGAGGTCCTTCAC | 11124 |
rs59582352 | in-del | -/C/CA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601740 | ATTCATATACACACA[-/C/CA]TATATTCATATATAC | 11124 |
rs59600829 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50939995 | AGCTCACTGCAACCA[C/T]TGTCTCATGGGTTCA | 11124 |
rs59622625 | snp | C/T | 0.268995 | 0.249277 | intron-variant | FAF1 | GRCh38.p7 | 1:50507592 | AATTTAAAAATTAGC[C/T]TGTAGTCCTAGCTAC | 11124 |
rs59635377 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766807 | AAAAAAAAAAAAAAA[A/T]AAAAACCACACATCC | 11124 |
rs59709788 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674259 | CAATTTTTTTTTTTT[-/T]ATTGTACCATGACAC | 11124 |
rs59743675 | snp | A/C | 0.0074973 | 0.0607655 | intron-variant | FAF1 | GRCh38.p7 | 1:50491713 | CAGAAGTACTTGACC[A/C]AGCCTACCTTTGCTC | 11124 |
rs59786222 | snp | C/T | 0.212425 | 0.24716 | intron-variant | FAF1 | GRCh38.p7 | 1:50830121 | TTTTGTTTTTTGGGT[C/T]TTTTTGGTTTTTTTG | 11124 |
rs59806816 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794808 | TTTTTTTTTTTTTTT[-/TT]GTATTTTGAGTAGAG | 11124 |
rs59844445 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50937369 | AAAATTAGGACTTAG[A/G]TAAGAGTTAATGCTA | 11124 |
rs59848467 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575366 | ATATACTATTTAGTA[A/G]AAATATCTAATTACA | 11124 |
rs59885358 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50818319 | TGGTGCAGCTACTTT[A/G]GAAACAGCATGGCAG | 11124 |
rs59930153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50713569 | ATGAGCCATCGCGTC[C/T]GGCCAAAAAACTACG | 11124 |
rs59965680 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50487628 | ATACTTTTCTAGATG[G/T]TTGATTTCACTCCAA | 11124 |
rs60014462 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50771007 | ACAAATGGGGAAAGG[C/T]TCCCTATTCAATAAA | 11124 |
rs60048959 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50938225 | AAAGCCAGGACTCTA[C/T]AGTTTCACACATTTC | 11124 |
rs60185039 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50853477 | GGTTGAAACATGTAG[A/T]TAAAGACAAATATAA | 11124 |
rs60244087 | in-del | -/AAAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50882646 | AATAAATAAATAAAT[-/AAAT]GTGTATGTATGTATG | 11124 |
rs60244988 | snp | G/T | 0.151001 | 0.229563 | intron-variant | FAF1 | GRCh38.p7 | 1:50908936 | TGTTAGCTGGTTACT[G/T]TCCTCATTAGTTGAT | 11124 |
rs60290409 | snp | A/C | 0.151001 | 0.229563 | intron-variant | FAF1 | GRCh38.p7 | 1:50938369 | GAGTCCTAGGACCAG[A/C]TATGTATGTCACCAG | 11124 |
rs60329786 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50891671 | GAGGCTGCAGAACAG[C/T]GAATACTGCTGAACA | 11124 |
rs60355854 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50577835 | ACGATATACTTAAAA[A/C/G]AAACATGAAAACTTA | 11124 |
rs60403650 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50708090 | TGGGGTTACAGGTGT[A/G]AGCCACAGCGCCCGG | 11124 |
rs60454536 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50889494 | CCTGCTTTCTCTTGT[A/G]GGCATTTAGTGCTAT | 11124 |
rs60483827 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50835985 | TAGGAGGGAAGTCTG[A/G]GCACAAAAGTAGCTG | 11124 |
rs60551908 | snp | A/G | 0.119978 | 0.213528 | intron-variant | FAF1 | GRCh38.p7 | 1:50921188 | ACCCTGCCCACAACC[A/G]CCAGAGCCTGGGTGA | 11124 |
rs60638627 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50708309 | TGTCAAGTTCAGAAT[A/G]TATTTTAGAGGTGGA | 11124 |
rs60719405 | in-del | -/ATTTT/ATTTTATTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674906 | ATTTTATTTTATTTT[-/ATTTT/ATTTTATTTT]GAGATGCAGTTTCGC | 11124 |
rs60720562 | in-del | -/A | 0.111576 | 0.20818 | intron-variant | FAF1 | GRCh38.p7 | 1:50669575 | AAAAAAAATTGGGGG[-/A]AAATAAGATTTCAAG | 11124 |
rs60756005 | snp | C/T | | | missense | FAF1 | GRCh38.p7 | 1:50596165 | GTGAAGATCTTCTTC[C/T]CACTGTAAGTCGATG | 11124 |
rs60756778 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50894330 | AAAAAAAAAAAAAAA[-/A]CTCCAAGGGCTCTTC | 11124 |
rs60779404 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50521018 | AACAGGACTGGCACT[C/T]ATACTGTTTTTTATA | 11124 |
rs60785372 | snp | C/G | 0.000399281 | 0.0141238 | missense | FAF1 | GRCh38.p7 | 1:50744695 | TCACACTGTCTTCCA[C/G]ATCTCCCGTCTTCCA | 11124 |
rs60788683 | snp | A/C | 0.174932 | 0.238463 | intron-variant | FAF1 | GRCh38.p7 | 1:50796981 | TCTCTACAAAAAATA[A/C]AAAAATTAGCCGGGC | 11124 |
rs60792426 | snp | C/T | 0.105924 | 0.204309 | intron-variant | FAF1 | GRCh38.p7 | 1:50523626 | TTAATTTTCTGTTGT[C/T]GTGTTGTAGGAGTTA | 11124 |
rs60826248 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50829472 | TCACCCCCAACAAAG[G/T]GACCTCTCATTAGAG | 11124 |
rs60832780 | snp | C/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50838042 | GCCACCGCGCCTGGC[C/T]GGATGCTCCTTTATA | 11124 |
rs60848584 | snp | C/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50544471 | TGATTAATGGCCACA[C/T]TTTGAGACACATTGC | 11124 |
rs60896591 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50612080 | GTATCTTAATAGTTT[A/G]AAAAATTTAAAAACC | 11124 |
rs60914341 | snp | A/G | 0.36021 | 0.224397 | intron-variant | FAF1 | GRCh38.p7 | 1:50948645 | TCAAGCGATTCTCAC[A/G]CCTCAGCCTCCCAAG | 11124 |
rs60944603 | in-del | -/AACA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50664823 | ACAAACAAACAAACA[-/AACA]GGTTATGTTTTCCTA | 11124 |
rs61047986 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828274 | TTTTTTTTTTTTTTT[-/T]CTTTCTTTTTTTGAG | 11124 |
rs61115731 | snp | C/G | 0.213333 | 0.247296 | intron-variant | FAF1 | GRCh38.p7 | 1:50932429 | AGGGCCCATTCAAGT[C/G]TGAAATCCAGCGGGG | 11124 |
rs61121387 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50681144 | CTCCGCCTCCCAGGT[C/T]CAAATGATTCTTCTG | 11124 |
rs61176999 | in-del | -/TGTGTG | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460829 | GTGTGTGTGTGTGTG[-/TGTGTG]CAGAGAAAGGGTCTC | 11124 |
rs61200472 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742167 | TAAAAAAAAAAAAAA[-/A]TTAGCCAGGCGTGGT | 11124 |
rs61258960 | in-del | -/TTTTTTTTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50497556 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GTGACGGAGTCTCAC | 11124 |
rs61273057 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50494848 | CTCAACAGTTATATA[C/T]TAGAAATTCAGAAGC | 11124 |
rs61286266 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50794206 | GGTTGAAAGCACATG[A/C]AGGTGAAAGCTGTAC | 11124 |
rs61350490 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | FAF1 | GRCh38.p7 | 1:50623400 | TGGCGAAACCCTGTC[C/T]CTACTAAAATACAAA | 11124 |
rs61376152 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50617712 | TTTTTTTTTTTTTTT[-/TT]AATAATTTCAGTAGC | 11124 |
rs61386942 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50720242 | CCTGACAGGTGATCC[A/G]CGTGCCTTGGCCTCC | 11124 |
rs61419821 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50676161 | CCTGTAATCCCAGCA[C/T]TTCGGGAGGCCGAGG | 11124 |
rs61462155 | in-del | -/TGTGTG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692288 | GTGTGTGTGTGTGTG[-/TGTGTG]GTGGGAACATTTAAA | 11124 |
rs61468246 | snp | C/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576641 | CCGCACCGCCCCCCC[C/G/T]CCGCCACCACCCCTG | 11124 |
rs61525573 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50867422 | AGTGGGAGAAAATCT[C/T]GGTAAATTATGCATC | 11124 |
rs61612294 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447142 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCCC | 11124 |
rs61643320 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50805228 | AAGAAGAACATCTTG[A/C]CTTGACCTAGTTTAT | 11124 |
rs61654181 | in-del | -/T | 0.493613 | 0.0561475 | intron-variant | FAF1 | GRCh38.p7 | 1:50448938 | TACGAGGGTCACAGC[-/T]TTTTTTTTTTTTTTT | 11124 |
rs61673645 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50808358 | ACCGCACAATTAAGA[C/T]GCGTAACAACCAGGT | 11124 |
rs61781009 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50447637 | ACCCTTTGCCACGCT[A/G]GCAGAAAATCTGTAA | 11124 |
rs61781010 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50451339 | TAACATTTATTGGGA[A/G]CTTACTAGGTGCTAA | 11124 |
rs61781011 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457025 | AGTTACTTCCCATTT[C/T]TGCATCTCAGTTTTT | 11124 |
rs61781012 | snp | C/T | 0.00836719 | 0.0641372 | intron-variant | FAF1 | GRCh38.p7 | 1:50475429 | GGCACATCTCCCACC[C/T]GGATATACTTCCTGA | 11124 |
rs61781013 | snp | A/C | | | missense | FAF1 | GRCh38.p7 | 1:50491726 | CCAAGCCTACCTTTG[A/C]TCTGTCAGCCTCAAG | 11124 |
rs61781014 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50514693 | GATGTTTAGAAAAGA[A/T]TCTTTTTCATCTGGA | 11124 |
rs61781015 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50536274 | TATGTGCCATTTCCT[G/T]AACACATTTAAGTCA | 11124 |
rs61781016 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50541790 | AAATAAAAAAAAAGG[A/G]AAAAGCAGGCAAGTT | 11124 |
rs61781017 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | FAF1 | GRCh38.p7 | 1:50546421 | TCTAGGCTGGAGTGC[A/G]GTGGTGCAATCTCAG | 11124 |
rs61781018 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | FAF1 | GRCh38.p7 | 1:50555757 | TTCAGCAATCCCACT[A/G]CTGAGTACCCAAAGG | 11124 |
rs61781019 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50559266 | AAAAAAAAAAAAAAG[A/G]ATAATCTGTTTTAAG | 11124 |
rs61781020 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50566286 | AATTGTTCTATAATC[A/G]TTTAAATTAGGTGAC | 11124 |
rs61781021 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50609792 | GTGAAGTTGAATTAT[A/G]GAAAAAAAAAAAAAG | 11124 |
rs61781022 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50633302 | GAACATGTATTGATT[A/C]TTTAAAGTTTTATTC | 11124 |
rs61781023 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50633808 | TGCCTGTCAAACCCC[C/T]GTGAGGTTTGATATG | 11124 |
rs61781024 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50656230 | CCAGCTACTTGGGAG[G/T]CTGAGGCAGGAGAAT | 11124 |
rs61781025 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50660516 | TTTTTTTTTTTTTCC[C/T]AAGACAGTCTTGCTC | 11124 |
rs61781026 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50660647 | TACAGGAGTGTGCCA[A/C]CACACCTGGCTAATT | 11124 |
rs61781027 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50664679 | GGCGCCTGTAGTCCC[A/G]GCTACTCAGGAGGCT | 11124 |
rs61781028 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683528 | TGAGACCCTGTCTCA[A/T]TAAAAAAAAAAAAAA | 11124 |
rs61781029 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50698114 | TTTATGAGCACTTTA[G/T]ATTCACTTACCCATC | 11124 |
rs61781030 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701988 | AACAGATAAGTAATA[C/T]TCCATAATTCTGCAC | 11124 |
rs61781031 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50710233 | TCTTGATCTTGACTG[G/T]CAGACTTGTGTAATA | 11124 |
rs61781032 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50714365 | AAAAAAAAAAAAAAT[A/T]AGCTAGGTGTGGTGG | 11124 |
rs61781033 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50722444 | ATGAGGTCAGGAGAT[C/T]GAGACCAGCCTGGCT | 11124 |
rs61781034 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50723256 | AAATACAAAAATGAG[C/T]CAGGTGTGGCGGCAT | 11124 |
rs61781059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50730970 | TCTCTGAACTTGCTT[C/T]CTATTGTGTTATATT | 11124 |
rs61782360 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | FAF1 | GRCh38.p7 | 1:50751886 | TTTTTGCGAAGGACT[A/G]GTAATAGTTCTTCCT | 11124 |
rs61782361 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | FAF1 | GRCh38.p7 | 1:50773221 | TGAGGCTTCAGTGGG[A/G]CATGACTGCATCACT | 11124 |
rs61782362 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50784312 | AAGAAAAAAAAAACT[A/T]AGAACTAATAAATAA | 11124 |
rs61782364 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803641 | GACTTAAAGCAGGCT[A/C]AGAAACACCTGGATA | 11124 |
rs61782365 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50813807 | AAATCCACAGCTTCA[A/T]TTAAAAAAAAAAAAT | 11124 |
rs61782367 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50818490 | CATCAACCAATGAAT[A/G]AACAGATTGAAGAAT | 11124 |
rs61782368 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830657 | CTTCCTCCAGTGCTC[A/T]ATTTTTTTTTTTTTT | 11124 |
rs61782369 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50831826 | AAAAAAAAAAAAAAG[A/G]ACTGAGACACAGAGA | 11124 |
rs61782370 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50835299 | TTCCAGTAATCCAAA[A/C]TGAGACTTAAGCAAT | 11124 |
rs61782371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841436 | GTAGTGTAAGATGGT[A/G]ACTTTCTCCTTTGTG | 11124 |
rs61782372 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50847418 | AAACTATGCCTGAAA[A/T]TAAAAAAAAAAAAAA | 11124 |
rs61782373 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50850144 | AAAAAAAAAAAAAAT[A/T]GAATGGTCAACAAGA | 11124 |
rs61782374 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | FAF1 | GRCh38.p7 | 1:50858311 | CAAAGATTCTCATGG[A/G]CAACCACATGTAAAA | 11124 |
rs61782375 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905383 | ATCATGATTCATAAT[A/C]CTTTGGATATATACC | 11124 |
rs61782376 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50912965 | TACATTCAACTCAAC[C/T]AACAGAAATGAACCA | 11124 |
rs61782377 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50918205 | AATTTTTTTTTTTTA[A/T]TTATACTCTAAGTTT | 11124 |
rs61782378 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940255 | AAGTACATTACCAGA[A/T]TTAAAAAAAAGTTAT | 11124 |
rs66503743 | in-del | -/TATCTTATTTTTAGAATAAGATATT | 0.221439 | 0.248363 | intron-variant | FAF1 | GRCh38.p7 | 1:50558203 | CGCATCCAGCCTAAA[-/TATCTTATTTTTAGAATAAGATATT]TATCTTATTTTTAGA | 11124 |
rs66702010 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50851082 | TGGAGCAATTTACAT[-/T]TTTTTTTTTTTTTTT | 11124 |
rs66707243 | in-del | -/TATTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674861 | CCTGTCACCTTGTAC[-/TATTT]TATTTTATTTTATTT | 11124 |
rs66856661 | in-del | -/AGAG/GAGA | 0.625 | 0.125 | intron-variant | FAF1 | GRCh38.p7 | 1:50527843 | AGAGAGGGAGAGAGG[-/AGAG/GAGA]GAGAGAGAGAGAGAG | 11124 |
rs67057333 | in-del | -/AAATACAGTGG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490541 | ACAGCTTCAGTATCA[-/AAATACAGTGG]AATACAACCCAGCTT | 11124 |
rs67168626 | in-del | -/AATA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50718034 | GCGAGACTCCGTCTC[-/AATA]AATAAATAAATAAAT | 11124 |
rs67753893 | in-del | -/CTG | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50849445 | TGCATTCTAAACACA[-/CTG]CTATCACTCATTATA | 11124 |
rs67974718 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50953950 | ATTCAGAAAGAATAC[-/A]TTTTTTTTTTTTATT | 11124 |
rs68136082 | in-del | -/TCAATT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789741 | CTCTTTCTCAACCCT[-/TCAATT]ACTCTCCTTTACTCT | 11124 |
rs71059589 | in-del | -/TGTGTGTG | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50472423 | CTTGGTTTTGGGGTT[-/TGTGTGTG]TGTGTGTGTGTGTGT | 11124 |
rs71059590 | in-del | -/AGGAAGGTAGAGCAGTGTGGTGTGGCGGCCCACCTAAAAAC | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50479226 | TGGCGTGATCCAGAG[lengthTooLong]ATTCTGCATCTTATA | 11124 |
rs71059592 | in-del | -/A/AA | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50640852 | GTGAGACCCAGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 11124 |
rs71059593 | in-del | -/TA | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50694005 | CATATATGTCATGTA[-/TA]TATATAATGACACAT | 11124 |
rs71059594 | in-del | -/TATGTCATATATATGTCATACATGTCATGTA | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50694038 | CATACATGTCATGTA[lengthTooLong]TATGTCATATATATG | 11124 |
rs71059597 | in-del | -/TATATATATATGTATATATATGTATATATATATACGTATATATATATG | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50819799 | ATATATATATATGTA[lengthTooLong]TATATATATATGTAT | 11124 |
rs71059598 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50836189 | AATGAGACCCTGTCT[-/A]AAAAAAAAAAAAAAA | 11124 |
rs71059599 | in-del | -/TCTTC | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50922506 | GGTTTTCTTTTCTTC[-/TCTTC]TCTTCTCTTCTCTCT | 11124 |
rs71059600 | in-del | -/TAT | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50931928 | CAGTCTTTCATGTGC[-/TAT]TATTATTATTATTAT | 11124 |
rs71059601 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50953961 | ACTCCGTCTCAAATA[-/A]AAAAAAAAAAAGTAT | 11124 |
rs71574409 | in-del | -/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50585080 | TTTGTCTTTTTCCCC[-/C]AGCATATAGTATACA | 11124 |
rs71574410 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50621420 | TTTTTTTTTTTTGAG[-/A]ATGGAGTCTCACTCT | 11124 |
rs71574411 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50621422 | TTTTTTTTTTTGAGA[-/T]GGAGTCTCACTCTGT | 11124 |
rs71574412 | in-del | -/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50733850 | GCCCAGGCTTGAGTG[-/G]CAGTGTTGCAATCTC | 11124 |
rs71575295 | multinucleotide-polymorphism | CT/TG | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50524328 | ATTTTTCTCCCATTC[CT/TG]TAGGTTCCCTGTTCA | 11124 |
rs71577268 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50922484 | CTTCTCTCTCTCTTT[A/T]CTTTTTTTTTTTTTT | 11124 |
rs71578049 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50736778 | GAAAGAAAAAAAAAA[-/A]GATGTCAAAATATTT | 11124 |
rs71578050 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50874036 | GGGTATGTGAGACCC[-/A]AAAATTTGGGGCTTA | 11124 |
rs71578680 | multinucleotide-polymorphism | AGCGATCA/GGTGATCT | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50524077 | CACACCAGTTAGAAT[AGCGATCA/GGTGATCT]TTAAAAAGTCAGGAA | 11124 |
rs71651146 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50491955 | TAAATAAGCAAACAA[A/C]CAATAAGATGAGCAG | 11124 |
rs71651147 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50493277 | ACCTCAAGTGATCTG[C/T]CTGCCTTGGCCTTCC | 11124 |
rs71651148 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50494696 | CTCACTGGTCCCTAC[C/T]TGAGCTGTACACTCC | 11124 |
rs71651149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518562 | TCTCCTGCCTCAGCC[A/T]CCTGAGTAGCTGGGA | 11124 |
rs71651150 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50553000 | TACAGGCATACAGAA[A/G]GTGAACAGGCGGGTC | 11124 |
rs71651151 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50559351 | TTCTCAATTGTAAGA[A/G]GCCATCACTTTTATC | 11124 |
rs71651152 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50663064 | TTCCTAAAGTGCTAA[A/G]AAAATGTTTATAGAT | 11124 |
rs71651153 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50663082 | AATGTTTATAGATGA[A/G]AAAAGCTAAACATAT | 11124 |
rs71651154 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FAF1 | GRCh38.p7 | 1:50712887 | TTCAAGTTGGGGGGG[C/T]GCTGTGGCTCACACC | 11124 |
rs71651155 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50737202 | GATAAAGTACTCATT[C/T]TCCAATAAACACTGC | 11124 |
rs71651156 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50737358 | TAATCACGCTACTGG[A/G]AAGCAACAGATTATA | 11124 |
rs71651157 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50749430 | ATAGCCTTTTGTTCC[A/C]CAGAAAGAGAGGAAT | 11124 |
rs71651158 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50777092 | AGTGAGACCCCATCT[A/C]CAAAAATGATAATAA | 11124 |
rs71651159 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50787703 | TAAAGTGTGATATGC[A/C]ATGTACTTGATTAGG | 11124 |
rs71651160 | snp | A/C | 0.046775 | 0.145601 | intron-variant | FAF1 | GRCh38.p7 | 1:50814616 | GCGAATAGTTAGATA[A/C]GTAAGAGTAAATACT | 11124 |
rs71651161 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50868877 | TTCTATCTGTTATTG[G/T]GTGGAATTGCCATTT | 11124 |
rs71651162 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50884373 | AAAGAAAAAAAAAAT[A/C]CAAAATTAGCCGGGC | 11124 |
rs71651163 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50885288 | TTCCCATTCTCTCCG[G/T]GTCTCTTTCTCTCTC | 11124 |
rs71651165 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50894132 | GGTGAAACTCCGTCT[C/T]TACTAAAAATATAAA | 11124 |
rs71651166 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50902786 | ATATGTAAGTAGCTG[G/T]TATACTGTATCTGTT | 11124 |
rs71659280 | in-del | -/GA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554400 | TATATAGAGAGAGAG[-/GA]AGAGAGAGAGAGAGA | 11124 |
rs71672961 | in-del | -/A | 0.234109 | 0.249494 | intron-variant | FAF1 | GRCh38.p7 | 1:50734734 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 11124 |
rs71699119 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50547418 | AATTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 11124 |
rs71713286 | in-del | -/CTCT | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50928181 | CACTTTTACTGCATG[-/CTCT]CTGTCTTTGGCACAC | 11124 |
rs71760943 | in-del | -/AAAC | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50664798 | GACTCCGTCTCAAAT[-/AAAC]AAACAAACAAACAAA | 11124 |
rs71765972 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50628133 | TGTGTATGCGTGTGT[-/GT]TTCTGTTAAGATGAG | 11124 |
rs71769751 | in-del | -/A | 0.332568 | 0.235971 | intron-variant | FAF1 | GRCh38.p7 | 1:50609794 | GAAGTTGAATTATGG[-/A]AAAAAAAAAAAAGTT | 11124 |
rs71812010 | in-del | -/CC | 0.257732 | 0.24988 | intron-variant | FAF1 | GRCh38.p7 | 1:50555294 | ACACACACACACACA[-/CC]CCCCAAAATAAAACC | 11124 |
rs71850142 | in-del | -/ACAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472369 | AATTGGGGAAAACAT[-/ACAC]ACACACACACACACA | 11124 |
rs71957678 | in-del | -/CC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527867 | CCTCTCTCCCTCTCT[-/CC]CTCTCTCTCTCTCTC | 11124 |
rs71962090 | in-del | -/TGTTTTTAGGTGGGCCGCCACACCACACTGCTCTACCTTCC | 0.0614824 | 0.164198 | intron-variant | FAF1 | GRCh38.p7 | 1:50479225 | CTATAAGATGCAGAA[lengthTooLong]TCTCTGGATCACGCC | 11124 |
rs71985016 | in-del | -/TTTTG | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50736870 | AAGGTTCTGCATGGA[-/TTTTG]TTTTGTTTTTTAAAT | 11124 |
rs72016541 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662684 | AAATGAATTTGTATC[-/T]TTTTTTTTTTTTTTT | 11124 |
rs72220248 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530239 | TAGCTTTAAGAAGTG[-/GT]GTGTGTGTGTGTGTG | 11124 |
rs72228005 | in-del | -/TACTT | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50442357 | GAATTAGAAAGACTC[-/TACTT]TAAATTACAGCTGTG | 11124 |
rs72249276 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601734 | ATATATATTCATATA[-/AC]CACACATATATTCAT | 11124 |
rs72690462 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50451292 | CCTGTTTGTTCTTTG[G/T]TTTATTAAATTATAA | 11124 |
rs72690463 | snp | A/T | 7.11098e-05 | 0.00596237 | intron-variant | FAF1 | GRCh38.p7 | 1:50452138 | ATAAAGAACATAAAA[A/T]GAATATACAAAGAAC | 11124 |
rs72690464 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | FAF1 | GRCh38.p7 | 1:50458271 | ATACATAAACAGTAA[G/T]AGTCACTCCATTTTA | 11124 |
rs72690465 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50478166 | GTTACAGTGGTGGTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs72690471 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | FAF1 | GRCh38.p7 | 1:50588898 | GCACTGGGGTAAGTG[A/C]TGGAGACAGAAACAG | 11124 |
rs72690472 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50597754 | GTCAATGATTGAAAT[A/G]TAAGGATGGTAAATC | 11124 |
rs72690473 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50602147 | GTAACACAAGTGAAC[A/G]AGATTCAAACTACAG | 11124 |
rs72690478 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50630409 | TAGGTAAGAACTATG[A/G]TAGCATTTTTGAACT | 11124 |
rs72690484 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50748162 | GTATAGTTGGTCTGC[A/G]AAGGACAGACAAACC | 11124 |
rs72690485 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50748814 | GACTGATTATATTAC[A/G]TATTAAAAGAAGAAA | 11124 |
rs72690486 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50754345 | CAGTATTTAATCTTG[G/T]ACTAGTACTCTCCAC | 11124 |
rs72690487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50767944 | TCAAATCCACACCTA[C/T]CAATATAAACTTTGA | 11124 |
rs72690488 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50781448 | AAAATGGTCAATTCA[C/T]CAGGAAGATATCCAT | 11124 |
rs72690489 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50782749 | TAAGGTTAATTCTTA[C/T]TAAAGAAATATATTT | 11124 |
rs72690490 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50785730 | CTATAGGAAACAGTA[C/T]GGAAGTTCCTCAAAA | 11124 |
rs72690491 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50787829 | AAACTTACCTCAATC[G/T]CAACACAGTATTTAA | 11124 |
rs72690492 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50793420 | AGTGAAAAATTAGAA[C/T]TGGAAGTGAAGTTTT | 11124 |
rs72690493 | snp | C/T | 0.376195 | 0.215812 | intron-variant | FAF1 | GRCh38.p7 | 1:50793907 | TCCAAAATCTGAAAC[C/T]TTTTGAGCACTGACA | 11124 |
rs72690494 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50802518 | GAGAGGTTTCCTTAT[A/G]TAAAACATCCCTAAA | 11124 |
rs72690496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808887 | ATCCAGCAGCACATC[C/T]AGTAAGGGCATTACA | 11124 |
rs72690500 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50840910 | AATGAAATACCACTC[A/G]GTCAAGAAAAAAATG | 11124 |
rs72690501 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50851367 | CGTGAGCCACTGCAC[A/C]AAGTCTAAATTTTTA | 11124 |
rs72690502 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50861373 | AGATGAGGTTATGAA[A/G]GTAGAATCTTCATGA | 11124 |
rs72692203 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50866702 | ATCATAGATGACACA[A/T]ATGGACACATCCCAT | 11124 |
rs72692205 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50876023 | GCAGCTCACTGTCTA[A/G]GAGGACAAAAGCATG | 11124 |
rs72692206 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50880383 | GGAACTGCATGTTTA[C/T]GCCCCTCCTCAATTC | 11124 |
rs72692207 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50882932 | CGGGTTGTAGTAAGC[C/T]GAGATTGCGCCACTG | 11124 |
rs72692208 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50883122 | GGAAACCCCTATTTA[A/C]GCACCTAGGATGCAA | 11124 |
rs72692216 | snp | A/C | 0.0115144 | 0.0749975 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50962232 | CTAAAAATAATACAA[A/C]AATTAGCTGGGCATG | 11124 |
rs72898910 | snp | C/G | 0.279461 | 0.248258 | intron-variant | FAF1 | GRCh38.p7 | 1:50442426 | CAATCTTGCAGGACT[C/G]ATTGTGAGAATTAAA | 11124 |
rs72898921 | snp | C/T | 0.161924 | 0.233971 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463103 | ATGAACACTTGCTTT[C/T]CTTCTGGGAGTCTGG | 11124 |
rs72898923 | snp | C/T | 0.144969 | 0.226867 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466011 | AGCTATTACAGGGTT[C/T]GAAAAGAGAAGTGAC | 11124 |
rs72898937 | snp | A/T | 0.289165 | 0.246913 | intron-variant | FAF1 | GRCh38.p7 | 1:50485134 | ATTATTATTATTATT[A/T]TTTTTAAATAGAGAT | 11124 |
rs72898944 | snp | A/C | 0.225301 | 0.248777 | intron-variant | FAF1 | GRCh38.p7 | 1:50492355 | CACCACACCACACCA[A/C]TAAAGCTCTGGTTAC | 11124 |
rs72898946 | snp | A/C | 0.192715 | 0.243348 | intron-variant | FAF1 | GRCh38.p7 | 1:50493590 | ATTAATTATCACATA[A/C]TTATTTATTTAATGC | 11124 |
rs72898950 | snp | C/T | 0.225005 | 0.248747 | intron-variant | FAF1 | GRCh38.p7 | 1:50495549 | AAATCTTGGCTACTG[C/T]GAACAATGCTGCAAC | 11124 |
rs72898951 | snp | C/G | 0.274929 | 0.248754 | intron-variant | FAF1 | GRCh38.p7 | 1:50497846 | TGCCACCGCGCCCGG[C/G]CTCAAAACTCTTTAA | 11124 |
rs72898953 | snp | C/T | 0.220544 | 0.248259 | intron-variant | FAF1 | GRCh38.p7 | 1:50498186 | CCTCAACAAATGATG[C/T]TAGGAAAGCTGGATA | 11124 |
rs72898956 | snp | G/T | 0.48 | 0.0979796 | intron-variant | FAF1 | GRCh38.p7 | 1:50499365 | TGTTAGCTGTAGGGT[G/T]TTTTTTTTTTTTTTT | 11124 |
rs72898957 | snp | C/T | 0.152001 | 0.229992 | intron-variant | FAF1 | GRCh38.p7 | 1:50500629 | GACCCAAAAGCATGA[C/T]ACATAAAAGAAAAAA | 11124 |
rs72898961 | snp | A/G | 0.114036 | 0.209795 | intron-variant | FAF1 | GRCh38.p7 | 1:50501304 | GCTGTCTCATTAATC[A/G]TCAAGAAAATGCAAA | 11124 |
rs72898963 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50502483 | TTCACTGGAGACTGG[A/G]GGCACATGAGCATTC | 11124 |
rs72898966 | snp | A/G | 0.225597 | 0.248806 | intron-variant | FAF1 | GRCh38.p7 | 1:50503899 | CAGACAGAGACAGCA[A/G]AGAGGGATGACAAAG | 11124 |
rs72898969 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50505036 | CTTCTGAGTGGGGGA[G/T]CTTACTGATCTTATA | 11124 |
rs72898971 | snp | A/G | 0.114738 | 0.210248 | intron-variant | FAF1 | GRCh38.p7 | 1:50505736 | TGTGACAGAAAGTAT[A/G]TGGTCCCCAAGGCCA | 11124 |
rs72898974 | snp | C/T | 0.110872 | 0.20771 | intron-variant | FAF1 | GRCh38.p7 | 1:50510299 | AACCTAATAATAATC[C/T]CAATAATATTAATCT | 11124 |
rs72898980 | snp | A/G | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50521075 | AAAATTGTATATATC[A/G]TGTATAATCTGATGT | 11124 |
rs72898982 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50523110 | CTTCAATCCTTTATT[A/G]AGGCTAAATAATATT | 11124 |
rs72898987 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50535881 | ACAAATCTATGAAGG[A/G]TTCATTATGATTTGG | 11124 |
rs72898990 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50538426 | TTTTAACTAAATACA[C/T]GGCAATGAAGAATAT | 11124 |
rs72898997 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50556913 | ATCAGTTTTCTTTAA[C/G]AACAGCAACTGACAC | 11124 |
rs72899000 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50566566 | TTTTTTTTCCCTATT[A/G]AGAATATGGATGTAT | 11124 |
rs72899002 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50585087 | TTTTTCCCCAGCATA[C/T]AGTATACAAGTAAGT | 11124 |
rs72900903 | snp | A/G | 0.119281 | 0.213102 | intron-variant | FAF1 | GRCh38.p7 | 1:50587913 | TCATAACTGGCATTA[A/G]AGCAAGCTTATAATT | 11124 |
rs72900906 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50590441 | AATTTTCTGTTCAGC[C/T]TGTTGACTGTTGGTT | 11124 |
rs72900917 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50617356 | GGGTTTTTATCAAGA[A/G]GTGATGTTCAGATTT | 11124 |
rs72900920 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50625733 | GTGAGGAACACAGGT[A/C]GGAAGGGAGGCACTG | 11124 |
rs72900922 | snp | A/G | 0.112631 | 0.208878 | intron-variant | FAF1 | GRCh38.p7 | 1:50629523 | TAATAGGTAAAATTG[A/G]GGAACTATGCTAGGA | 11124 |
rs72900924 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50631543 | TTGGCAATTCAGATA[C/T]GACAAAGAGAAGCCA | 11124 |
rs72900926 | snp | C/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50635944 | GGCATATGGTTTGGC[C/G]AGTGTAAATGCAATT | 11124 |
rs72900928 | snp | G/T | 0.115088 | 0.210473 | intron-variant | FAF1 | GRCh38.p7 | 1:50637508 | AGGAACACTAGCTCT[G/T]TCACATTTCCATACA | 11124 |
rs72900932 | snp | C/T | 0.115088 | 0.210473 | intron-variant | FAF1 | GRCh38.p7 | 1:50642287 | TGTTTAGTGTTTGGA[C/T]GGCAAATATTTTTAT | 11124 |
rs72900933 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50642686 | AATAAAATTCTTGTA[A/G]TCAGTTGAATCTTGT | 11124 |
rs72900936 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50645310 | AGAATGCTTCTGATT[A/C]TGCATGTGTATGCAA | 11124 |
rs72900938 | snp | C/T | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50652855 | TTATCTTAATTATAA[C/T]GTCGACTCATTTACT | 11124 |
rs72900940 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50658907 | AATGCTGTTACCATA[C/T]GTAGATGTTACCAGT | 11124 |
rs72900944 | snp | C/T | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50661242 | TGTCACACTGGTTTC[C/T]CAGAAAACTATTCTA | 11124 |
rs72900956 | snp | G/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50677993 | AAAATGGTGAGTTTT[G/T]TGAGATATGTAGGCT | 11124 |
rs72900957 | snp | A/G | 0.110872 | 0.20771 | intron-variant | FAF1 | GRCh38.p7 | 1:50680136 | GTTGAAGAAACATTT[A/G]TCTCTGATAGTGTAT | 11124 |
rs72900967 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50694547 | TCTTCTATAACACTA[C/T]AGCCAGGAAAAAAAA | 11124 |
rs72900979 | snp | C/T | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50724642 | TTAAATGAGAAAATA[C/T]GTAGCTTTCCCACTC | 11124 |
rs72900982 | snp | C/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50724787 | CAGTTTCCTCTTTCA[C/T]TTCCTGTGCCCTAGT | 11124 |
rs72900983 | snp | C/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50727084 | ACTCTGCCCTTCACT[C/T]AGATGGCCCCTCCAT | 11124 |
rs72900998 | snp | C/T | 0.138207 | 0.223612 | intron-variant | FAF1 | GRCh38.p7 | 1:50740088 | TAGCCACTGAGAATA[C/T]AGCATTGAACAGAAC | 11124 |
rs72901000 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50742422 | AGACTCTTGCTCTGT[C/T]GCCCAGGATGGAGTG | 11124 |
rs72902703 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50745461 | AAATCTCATGTCAAA[C/T]TGTAATTCCCAGTGT | 11124 |
rs72902706 | snp | A/C | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50747124 | TGAGGTTGGACCCCC[A/C]CACACACAGTCTCCA | 11124 |
rs72902708 | snp | C/T | 0.211212 | 0.246973 | intron-variant | FAF1 | GRCh38.p7 | 1:50748005 | TAGCCTGCAGAACTG[C/T]GAACCAATTAAACCT | 11124 |
rs72902722 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50757330 | TGTTATAATCTCCAA[C/T]TGTGAATTTATCCAT | 11124 |
rs72902726 | snp | C/T | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50757828 | CTTCATTGGGGATTT[C/T]TGAGTATTTTTTAAG | 11124 |
rs72902729 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50766263 | TTAACATGTTTTATA[A/G]TATGAGAAATCATTC | 11124 |
rs72902736 | snp | A/G | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50774304 | GAACATTTAACTAGT[A/G]TTTATTACTCATAAA | 11124 |
rs72902742 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50777671 | CAGATGGCTACCAAG[C/T]TAGAAAAAAGATTTC | 11124 |
rs72902744 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50777970 | CTTGAAGGTCAAAAG[A/G]AGAATGTTTATGTAT | 11124 |
rs72902748 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50779722 | GAAGTTAGATTGTTA[C/T]CAGCTTAAAATAGAT | 11124 |
rs72902751 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50781678 | CAGACATATACTGAA[C/G]ATCCATTCTATCACA | 11124 |
rs72902755 | snp | G/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50785236 | GGCAATGGTTTTTTG[G/T]AAATGACTCCAAAAG | 11124 |
rs72902760 | snp | A/C | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50786799 | ACTAGAAATGCAGGT[A/C]GGGGCTTGATCAAAC | 11124 |
rs72902763 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50789648 | TAACTAATCCCTTTA[C/T]ATGTACTCCTGCAAC | 11124 |
rs72902765 | snp | G/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50791026 | CATTGTAAATCATAC[G/T]CCAAAAAGTTCAAAA | 11124 |
rs72902767 | snp | A/G | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50795327 | CTTGACTTGCCTGAC[A/G]GCAATGCATCTGTCA | 11124 |
rs72902768 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50796293 | AGTGACATATCACCC[C/T]AACACTGGCACTCAT | 11124 |
rs72902772 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50799696 | CTATAGTATTTGATA[C/T]CTCCTTTCTTTGTTA | 11124 |
rs72902776 | snp | A/G | 0.151668 | 0.229849 | intron-variant | FAF1 | GRCh38.p7 | 1:50804282 | AAAAATCACAGCTAC[A/G]TTCAAGAAAGCAACA | 11124 |
rs72902777 | snp | C/T | 0.117886 | 0.21224 | intron-variant | FAF1 | GRCh38.p7 | 1:50806606 | CTGAGACAAAGGGCA[C/T]TGGCTAGCACCACCC | 11124 |
rs72902778 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50811043 | GTGAGACTCTGTCTC[A/G]AAAAACATGGACCAG | 11124 |
rs72902785 | snp | A/G | 0.165527 | 0.235296 | intron-variant | FAF1 | GRCh38.p7 | 1:50825158 | GGTGATGGATATCCT[A/G]ATTACTGATTGTATC | 11124 |
rs72902789 | snp | C/G | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50827934 | TGTTAATTCTTCCCA[C/G]ATTCATCTTCAAATC | 11124 |
rs72902792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50831524 | GTCTTTCTCTACACC[A/G]TCCCCTTGTACAGTG | 11124 |
rs72904709 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50840330 | GCCGGCCACATACCA[A/G]AAATGTGTTTATTCT | 11124 |
rs72904713 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50847320 | AACAGGAAATTTTAG[A/G]TGACTATGATTAATA | 11124 |
rs72904718 | snp | C/T | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50849784 | CAACATAGCATTACA[C/T]TAGAGCTACTTAAAT | 11124 |
rs72904719 | snp | G/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50858874 | GTGACCCAGCTCATG[G/T]CAGTGTAGGCATTTT | 11124 |
rs72904720 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50861984 | AAGCCAACCAGACTA[C/T]TGTATTTTGTTATGA | 11124 |
rs72904723 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50868632 | TTCAAAGTTTTTTCT[A/G]AAGTTTTCCTCATGA | 11124 |
rs72904725 | snp | C/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50868816 | TGAAGACTTAATAGC[C/T]CAATAATCTGTATTG | 11124 |
rs72904726 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50873660 | TTACCACTCCTTTTC[C/T]AGGGATTTCTGAAAA | 11124 |
rs72904730 | snp | C/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50876363 | CAATAAAAGGAACCA[C/G]TGTTCCTTGTAGAAA | 11124 |
rs72904732 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50877137 | CAAGGGCGACAGCAC[A/G]GGTAGTGGGGAGAAA | 11124 |
rs72904734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50877710 | TAAGTACCCTCCTGG[C/G]CAGGAAGAAATGCTT | 11124 |
rs72904737 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50886174 | TTACTGTTGCCAGTG[A/G]TTTATTTTACCCTCA | 11124 |
rs72904745 | snp | C/G | 0.110872 | 0.20771 | intron-variant | FAF1 | GRCh38.p7 | 1:50897601 | GAGAAAAATGGCTGA[C/G]AGTGTAAATGTTCAC | 11124 |
rs72904749 | snp | C/T | 0.208474 | 0.246527 | intron-variant | FAF1 | GRCh38.p7 | 1:50901748 | TGCATGCTTGAGGTC[C/T]CAGCTACTAGGGAAG | 11124 |
rs72904754 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50905588 | CATTGTAACTGTGAG[A/G]TGGTATCTGATTGTG | 11124 |
rs72904767 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50923111 | ATAATGAGCAACAAG[A/G]TTGAATCAGTAATAA | 11124 |
rs72904771 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50927740 | ATTTTTTTTCTTACA[A/G]TTCTGAGACTAGAAA | 11124 |
rs72904783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943694 | CAGGAAGTTTCCCCA[A/G]GCAAGCAAGCATGGC | 11124 |
rs72904788 | snp | G/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50949575 | TAAATATTTTAGGCT[G/T]TGCAGGACATGCAGT | 11124 |
rs72904790 | snp | C/T | 0.21845 | 0.248001 | intron-variant | FAF1 | GRCh38.p7 | 1:50949980 | TACAAGCACATGCTA[C/T]CACACCCAGCTAATT | 11124 |
rs74080003 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | FAF1 | GRCh38.p7 | 1:50548299 | TTAGTGGTTCAGATG[A/T]AGTGCTGGGGAAAAT | 11124 |
rs74080004 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50551166 | AGATTATGAGATTAC[A/G]TATAGCTATTATGTC | 11124 |
rs74080005 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50562696 | TAGCTCTTATGTCTG[C/T]TTTGCCTACTAGACT | 11124 |
rs74080006 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50562699 | CTCTTATGTCTGTTT[G/T]GCCTACTAGACTATA | 11124 |
rs74080007 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50579625 | GTCACCTAAATCTAA[C/T]AAAGCTTTTAGACCT | 11124 |
rs74080008 | snp | G/T | 0.297833 | 0.253419 | intron-variant | FAF1 | GRCh38.p7 | 1:50582045 | TAAAACCTTTTTTTG[G/T]GGGGGTGGGCAGGGG | 11124 |
rs74080009 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50582925 | AAGTACACTTAGCAA[A/G]TGAATTTAATAAGTG | 11124 |
rs74080010 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50585590 | TGGGCTGTAAATACT[G/T]CTGAATATTCATGCC | 11124 |
rs74080011 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50587367 | AAAAGCCAATTTTGT[C/T]GAAAAAAGTATATTT | 11124 |
rs74080012 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50589453 | TGTCAAGGCTGCTGG[A/G]CTGTGTTCCCAGGCC | 11124 |
rs74080022 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50589454 | GTCAAGGCTGCTGGG[C/T]TGTGTTCCCAGGCCA | 11124 |
rs74080023 | snp | A/T | 0.0785177 | 0.181917 | intron-variant | FAF1 | GRCh38.p7 | 1:50589564 | AGGAGTTCTCTATAT[A/T]TTATAGACATTGATC | 11124 |
rs74080024 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | FAF1 | GRCh38.p7 | 1:50596047 | ATTGCTCTGGCAGAT[A/T]AAAAAAAAGGGAAGT | 11124 |
rs74080025 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50607850 | AATCCCAGGTGGGAA[C/T]TGAGTAGACAGAGGC | 11124 |
rs74080026 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50611958 | AGGGCAAAATAATGA[C/T]GCTGAGCAGGAAATT | 11124 |
rs74080027 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50626734 | AGTGTTATTCTGATA[C/T]AGTACGGAGAGTTGA | 11124 |
rs74080028 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50626991 | GATGGATTGTGATGC[C/T]ATTCATGGAATTAGA | 11124 |
rs74080029 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50632910 | TAGTTATTTCTCGAA[C/T]TGCTTTCCTTCTCAG | 11124 |
rs74080030 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50633977 | AAAAGAACAAAAAGA[C/G]TTTCATTGGCTCTGG | 11124 |
rs74080031 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50634622 | AACCTGTTTGTGGTT[G/T]TTGTTTGTTTTAAAG | 11124 |
rs74080033 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | FAF1 | GRCh38.p7 | 1:50635000 | CTACTACTTGGCTCA[A/G]ATAAGATCATGTACA | 11124 |
rs74080034 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | FAF1 | GRCh38.p7 | 1:50636266 | TATAATTTTCAAATT[A/G]TAGAAAATTTCCATC | 11124 |
rs74080035 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | FAF1 | GRCh38.p7 | 1:50636959 | ACAAACTGTCTCCAC[C/T]GCATTACTTTGTTAT | 11124 |
rs74080036 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50637041 | CTCTATTTTACCTAT[C/T]GATTTATGTCTGTCT | 11124 |
rs74080037 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50637712 | GTGTGTGTGTGTGTG[C/T]GCGTGTGCATATGTG | 11124 |
rs74080038 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50650936 | GAGTACAAAAGGAAC[A/G]GAGTTACTGACAATT | 11124 |
rs74080039 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50652405 | TTACAGGCAGAAGAA[C/T]TGATCATATTTCATC | 11124 |
rs74080040 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50654640 | GAGATTAAAGTGTTA[C/T]TAACTATAAAAATTA | 11124 |
rs74080041 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50665215 | CCATTTTGTGAAATT[C/G]AATTTTATATAACAC | 11124 |
rs74080042 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50668849 | ATCAGGAAAAAAAAT[G/T]TAACCACATGATTCA | 11124 |
rs74080043 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50671477 | ATCTAATTTTCATCA[A/G]TCCATACATTCACAA | 11124 |
rs74080045 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50679413 | TCCTCAGTAACCCTA[C/T]TAAATAGATGGCATT | 11124 |
rs74080046 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50685398 | GTAGCGAGATAGAAG[G/T]AGGGTGAGGTAAACT | 11124 |
rs74080048 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50706696 | TAAATGAGTATTAAA[C/T]TAATATTAGAAATAT | 11124 |
rs74080049 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50708266 | GACAGTAGCTTGGAC[A/T]AAGGTGGTAGAGGCA | 11124 |
rs74080051 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50711464 | GTTATCCACACTGAC[A/T]TTTTTTTTTTTTTTT | 11124 |
rs74080052 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | FAF1 | GRCh38.p7 | 1:50716322 | AGTAGACAGAAGAAT[C/T]AGCTAAACTAACCCA | 11124 |
rs74080053 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50718866 | TTTAAATTAAAAAGC[C/G]TGACACATGGCAATT | 11124 |
rs74080067 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | FAF1 | GRCh38.p7 | 1:50722943 | TAGCTCCTTCCAAAG[A/C]TGGTATCCTAGAGCT | 11124 |
rs74080069 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50737349 | AAATCCATTTAATCA[C/T]GCTACTGGAAAGCAA | 11124 |
rs74080070 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50740749 | TACAATTTACCAGGA[C/G]ACATGGACATCCTGA | 11124 |
rs74080072 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50754401 | GTGTAACCAAAGCCA[C/T]ATGAATTATGAGGTT | 11124 |
rs74080073 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50758570 | ACAGAAAAGGTTTTT[A/T]AAAAATGTGTAACCA | 11124 |
rs74080074 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50766808 | AAAAAAAAAAAAAAA[A/T]AAAACCACACATCCA | 11124 |
rs74080075 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50776965 | GGTGATTTAAAAAAA[A/T]ATATACAGAATCAGC | 11124 |
rs74080076 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50778271 | GGAGATTAAATTGCT[A/G]GTAGGAGGAATGAGA | 11124 |
rs74080078 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50790757 | AAGAACAATGTTCAA[C/T]TGTTCATACAATTAA | 11124 |
rs74080079 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50793851 | TAAGCAGCAAGTATA[C/G]GTTAAGTCTCCCTAA | 11124 |
rs74080080 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50795957 | GGGCATGTCTAGTAA[G/T]AATGGAAAATTACAA | 11124 |
rs74080081 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50796059 | AAAAAACAACAACAA[A/C]AAAAAAAAACAAAAA | 11124 |
rs74080082 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50802467 | AAACCTAACACCATG[A/G]CTATTAACAGGTAAC | 11124 |
rs74080093 | snp | A/C/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50819037 | CAAAATTTTCTACTT[A/C/G]TGGCATCATGTTGGC | 11124 |
rs74080094 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50830402 | GGCGTGAGCCATTGC[A/G]CCCAGCACCACAGGG | 11124 |
rs74080095 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50831655 | TATAGTGGGTTGAAT[A/T]GTGTGTCTAAAAAAT | 11124 |
rs74080096 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50842396 | AAAACCATTTTGTAA[C/T]CCAAACCAGTATAAT | 11124 |
rs74080097 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50844281 | CTGGTTTTTAATCCC[A/G]TCAGGTGAATAGTTT | 11124 |
rs74080099 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50853125 | CTATTCATTCATAAA[A/G]CTGCAGGTGTTCATA | 11124 |
rs74080102 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50897773 | ACTAGGCTCAGACAT[A/G]TGACTTTACTCTATC | 11124 |
rs74082103 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50913590 | TTCATCAAGAGTAAA[C/T]TGTCAGCAACAGCAG | 11124 |
rs74082105 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50931220 | GGTTCTCAGTTTACT[A/G]TCTTGGTTCTTTTAT | 11124 |
rs74082106 | snp | A/G | 0.031825 | 0.122064 | intron-variant | FAF1 | GRCh38.p7 | 1:50938059 | TTATTAGGCACAATC[A/G]CTTATACTGACAAAA | 11124 |
rs74082107 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50940423 | CACTATACCATTATG[C/T]TTCTGTTGTTCATTT | 11124 |
rs74082108 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50949345 | TCAACATTTTGAGCC[A/C]GAAAATTCTTTACTA | 11124 |
rs74082109 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50949755 | AGTTATCTGAATTAC[A/G]ATTGATTGTCCTCAG | 11124 |
rs74082110 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50951799 | GTTTGGTCCCTAATC[C/T]GCAACATCACAAAAG | 11124 |
rs74082524 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441040 | CAGTCATGAAAATAA[A/G]AAGACATATATCAAA | 11124 |
rs74082526 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50445863 | TAATCATTTAGCAAA[C/T]TGGCTTTGTGAAACA | 11124 |
rs74082527 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50448982 | TGGTCTTGATTAAAA[A/G]ATGGGAAAATCAACT | 11124 |
rs74082529 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50455188 | GCTGACAGTAAGTCT[C/G]CATCAGTTGCCCTTT | 11124 |
rs74082530 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461550 | TAAGACAGTATAGCT[A/G]CTGCCCTAAATGAAC | 11124 |
rs74082532 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463810 | CACATCGGAGATCCA[C/T]CACCTCTTGGAAGGC | 11124 |
rs74082533 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50480637 | CACACATAAGAAAAG[A/G]TAGTATGTGCCACAT | 11124 |
rs74082535 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50487489 | TCATGTAAGTTTCTT[G/T]AAACTGATTTTGGAA | 11124 |
rs74082538 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50496290 | CTTGTCATCAGAGAC[A/G]TGGCCCTGCTATCTA | 11124 |
rs74082541 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50501104 | GAAAGTCATAGTGAC[A/C]AAACCATAGACTGAG | 11124 |
rs74082543 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50517125 | GCAGTATTTTTCTAA[C/T]AAAAGTGCATGTACA | 11124 |
rs74082544 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50521343 | AAAAATTCATGAGGA[A/C]TATGACTGTCTCCAA | 11124 |
rs74082547 | snp | C/T | 0.106633 | 0.204807 | intron-variant | FAF1 | GRCh38.p7 | 1:50538651 | TCTACAAACCACACC[C/T]TGAGAAACACTAGTT | 11124 |
rs74082548 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50547927 | TAAGTACTTGAAAAT[G/T]TCTTCATAAAAATGG | 11124 |
rs74329106 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50703408 | CAGGTGTTGCACAAG[C/T]TGAAGCAGAAAAGTC | 11124 |
rs74343551 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50878929 | TGTCTCTCTTGTTAA[A/C]TGTTACTAAATGAAA | 11124 |
rs74349886 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50640310 | GTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCGC | 11124 |
rs74367063 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50639126 | TATTGTATCTATCAG[C/T]AGTTTGCTGCTTTTC | 11124 |
rs74396767 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50747067 | TGTCCAGGCAGAAGC[C/T]CTCATGGAGAATCTC | 11124 |
rs74411796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50847085 | TTTGTTTTCATTTCT[C/T]TGTCAGTGAGGACTT | 11124 |
rs74419151 | snp | C/G | 0.106278 | 0.204558 | intron-variant | FAF1 | GRCh38.p7 | 1:50563065 | TGGGAGGATGTGCAT[C/G]GGTTATATGTAAATA | 11124 |
rs74423262 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50639936 | AAGACTCGATCTCAA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs74423539 | snp | G/T | | | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462289 | ATATCGATTTTTAAA[G/T]GCTCACTACATGCCT | 11124 |
rs74493426 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50597977 | TTCTACTATTCACTC[A/G]AATCAATATTTTCCA | 11124 |
rs74498039 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50883405 | CTAAGTATCACAAAT[A/G]CTAAGACAACGTCAG | 11124 |
rs74499206 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50847573 | ACTGAAACACACTGA[A/G]AAGAACAAACAAAAG | 11124 |
rs74502293 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50800603 | GGGGTATAGGTCTAT[G/T]TTATCATTGCTTTCA | 11124 |
rs74504834 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50789023 | TTTTTTTGTAGAAAC[C/G]GAGTCTTGTTAATGT | 11124 |
rs74507064 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50690233 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 11124 |
rs74508207 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50777408 | AACCTGGGTGACACA[C/G]CAAGACTCTGTCACT | 11124 |
rs74510374 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648463 | CATTCATTCAACAAA[C/T]ATTTATCAAGTATTT | 11124 |
rs74526277 | snp | A/G | | | missense | FAF1 | GRCh38.p7 | 1:50584687 | TATTAATACTCACTC[A/G]TTGGAGATTTTCTCA | 11124 |
rs74532588 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50639462 | ATGCTTTTCCAGGAC[C/T]TTATTCACCTGATTG | 11124 |
rs74539268 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50803221 | CTTTACTAAGTAACA[A/G]TAAATGGTTAAGAGA | 11124 |
rs74542839 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50520360 | GTGACATGTCAAAAA[C/T]ACTAATGGAAGGCAA | 11124 |
rs74550555 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50860307 | AGAAACTATCAACAG[A/G]GTAAACATACAACCT | 11124 |
rs74556469 | snp | A/C | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50927542 | TGAGACCCTGTCTCC[A/C]AAAAAAATAAAAGCT | 11124 |
rs74576709 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50786750 | GTCCATTATGGCATA[G/T]GCATAGTGAACTAGG | 11124 |
rs74580662 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50732905 | CTTCTTTTTTTTTTT[A/G]GTGTTTATTCTCTTT | 11124 |
rs74587801 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527870 | CTCTCCCTCTCTCCC[C/T]CTCTCTCTCTCTCTC | 11124 |
rs74613980 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50577126 | GTTTCCTCACTTTAA[C/T]CTTCCATTGCCTTTA | 11124 |
rs74619768 | snp | G/T | 0.277778 | 0.248452 | intron-variant | FAF1 | GRCh38.p7 | 1:50770368 | AACTCCATAACCTCT[G/T]TCCAAAAGTTCCTAG | 11124 |
rs74621392 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50684901 | ATAGTACCCCTCCTC[C/G]AAGAGTATATAGGCT | 11124 |
rs74629821 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50919762 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCGAAGA | 11124 |
rs74639705 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50883597 | ACTATCCTGGACCCC[A/T]CACAAGTTAATGTTA | 11124 |
rs74643150 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50861261 | ATTAAAAACAAGAGA[C/T]TGCTATGGATTGAAT | 11124 |
rs74648981 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50684280 | TTTTTTTTTTTTTTG[G/T]TTCAAACTCTGAAGC | 11124 |
rs74683556 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50801066 | TAATTCTCTTGGCCA[C/T]ATCTTCCAGTTTTAC | 11124 |
rs74683936 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50757038 | GTTTATTTAGGAATA[C/T]GTTGTTTAATTTCCA | 11124 |
rs74686822 | snp | C/G/T | 0.00875412 | 0.0656548 | intron-variant | FAF1 | GRCh38.p7 | 1:50503324 | CCATAAAAAATTGTA[C/G/T]AGATATTGTTAATGG | 11124 |
rs74700695 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50911014 | CATCTTGGAACCTCC[A/T]TTCACCTTCCTTTTT | 11124 |
rs74708126 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50785153 | AAAAAAAAAAAAAAA[A/G]AAGACTTGAAACTAT | 11124 |
rs74711696 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50927284 | GAATTTTTTTTTTAA[A/G]GCTTACTGCATGGGG | 11124 |
rs74727214 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50946554 | TCCAGAATGTCACGT[A/G]TCTGTCAACATCCAT | 11124 |
rs74729038 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50676473 | TTTCAGTAAAAAAAA[A/G]GAAAAATGTAAATAT | 11124 |
rs74734499 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50790501 | TTTATACATAGGAGG[C/T]ACTCAAATATTTGCC | 11124 |
rs74738164 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50612551 | AGTCAATAGTGAGAT[A/G]CCATTTACCCCTCAA | 11124 |
rs74756335 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592933 | ACAGAGCAAGACTCT[A/G]TTTCAAAAAAAAAAA | 11124 |
rs74777408 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50784796 | TTACAAAGCTAGAGT[A/C]ATTAGATCAGTTTGT | 11124 |
rs74780881 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | FAF1 | GRCh38.p7 | 1:50686694 | TTAATATCAAACTCA[A/T]GAAAACTGTATCCAA | 11124 |
rs74784988 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50603157 | TCTTGTCTTACTATC[C/T]GATAACCAGTAATTA | 11124 |
rs74827444 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50455697 | AAAAAGACCCAGAGA[C/T]GTATGTACCTTGCTT | 11124 |
rs74830103 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50733714 | CTACTGGAACCTTCA[C/T]CTTGGAGATTTCCAA | 11124 |
rs74863417 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50771573 | CCACAATGAGATACC[A/G]TGTTATACCAGTCAG | 11124 |
rs74871284 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50564966 | ATTTGTTTTTTTTTT[A/T]TTACTTGCTTTTTAA | 11124 |
rs74886057 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50837761 | CCTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCAC | 11124 |
rs74902190 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490540 | TAACAGCTTCAGTAT[C/G]AAATACAACCCAGCT | 11124 |
rs74904376 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | FAF1 | GRCh38.p7 | 1:50763986 | ATTTTCTTTATATAC[C/T]TCAACAGAAGTAACA | 11124 |
rs74905420 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50694527 | CATAGTAATGATTAT[A/G]GATCTCTTCTATAAC | 11124 |
rs74925851 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50714363 | AAAAAAAAAAAAAAA[A/T]TTAGCTAGGTGTGGT | 11124 |
rs74925918 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50686550 | TCTATCTCAAAGAAG[A/G]GGAGGGGAGGGGAGG | 11124 |
rs74929692 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50899508 | AGTCTCACTCTGTCA[C/G]CCAAGCTGGAGTGCA | 11124 |
rs74929965 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50484801 | TTTATCAGGCTTATA[A/C]GTTAGGTAAAAATTT | 11124 |
rs74942898 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50807935 | AGGTACTATAAAAGA[C/T]GACCTTGCCCAAGAC | 11124 |
rs75009771 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50678394 | TAAGTTATCCAAAAC[A/C]TACAAATTAGTACTT | 11124 |
rs75013786 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50555363 | GGAGAAAATACATCC[A/G]ACAAAGGATTACTAT | 11124 |
rs75019420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50475401 | TTGAACTACTTTGTT[C/T]AGCTTTAATGATGGC | 11124 |
rs75029011 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50524893 | TTGGTCCCATATGAA[A/T]TTTTTTTTTTGAGAC | 11124 |
rs75038278 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50712661 | ACTCTGTTGTAAAAG[A/G]AAAAAAAATGCCATG | 11124 |
rs75039701 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50654988 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTTTCGCT | 11124 |
rs75042220 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50738443 | AGTGAAACTCCGTCG[A/C]AAAAAAAAAAAAAAA | 11124 |
rs75055136 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465948 | GAGGGGTCAGAGAAA[C/T]GCCAGCAAGTTAGAT | 11124 |
rs75063675 | snp | G/T | 0.16911 | 0.236552 | intron-variant | FAF1 | GRCh38.p7 | 1:50582940 | ATGAATTTAATAAGT[G/T]CTATAAAACCATGCC | 11124 |
rs75069849 | snp | G/T | 0.279726 | 0.248226 | intron-variant | FAF1 | GRCh38.p7 | 1:50880687 | ACTGTGAGAAAATTT[G/T]TTTCTGTTGTTTAAG | 11124 |
rs75081331 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50689889 | AACAAAAACAAATTT[C/G]TACCCATTAAACATT | 11124 |
rs75101698 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50565204 | ATTTTGAATAAGGAT[A/G]CCAAGTATCTTAAAT | 11124 |
rs75151105 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50495080 | CATGGAAAGTGGGGT[G/T]TCCGTCCCCTCAAGC | 11124 |
rs75177467 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50673628 | CTGTGATGGGTGATA[A/C]GAGACTCTTGACAGT | 11124 |
rs75212675 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50904809 | CTGAAACAAATATAA[C/T]TACTACCCAACTAAA | 11124 |
rs75215302 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | FAF1 | GRCh38.p7 | 1:50455584 | TCAATGGGGCATGTA[C/T]TATCAACATCCAGGT | 11124 |
rs75228088 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50491196 | TTTCCACTGAAACTC[C/T]TACTCACTGAACTCT | 11124 |
rs75228748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50484583 | ACATATTAATTGTGC[A/G]ATAGTGGTGATAATG | 11124 |
rs75240124 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | FAF1 | GRCh38.p7 | 1:50833342 | TACAGGCTTATTATA[A/T]AAAAAAAAAAGAACT | 11124 |
rs75242859 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50791276 | ACATCTAAAGCTTGT[A/C]ATAACTTCTCAGAAC | 11124 |
rs75253937 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50448939 | ACGAGGGTCACAGCT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs75255087 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50618729 | AACATTTGTTTTATC[A/G]AATATAAGAATAGCA | 11124 |
rs75273373 | snp | C/G/T | 0.0938545 | 0.199427 | intron-variant | FAF1 | GRCh38.p7 | 1:50489266 | AGCACAGGTCTTCTT[C/G/T]AAAAAACATTTGTTA | 11124 |
rs75273935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50529617 | AAGAAAGAACCCAGC[A/G]TGTAGCAGGAAGCTG | 11124 |
rs75291690 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50444757 | CAACAGCTCAGTGAA[A/G]TAGGTACGATTCTTT | 11124 |
rs75333002 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50590983 | CGAGACTCTGTCTCC[A/C]AAAAAAAAAAAGAAA | 11124 |
rs75348538 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50849117 | CACACACAAAAAAAA[A/T]TTATCCAGGAGTGGT | 11124 |
rs75378640 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50740013 | CTTTACATCATAAGC[C/T]AGGAAATGCACTTAT | 11124 |
rs75380251 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | FAF1 | GRCh38.p7 | 1:50538067 | TGGTTCACTGAGTTA[C/T]GCATTTCTCTGCTGA | 11124 |
rs75392349 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50803192 | ACAGCATTGGTTCCA[C/T]GTACATGTATCTCCT | 11124 |
rs75392698 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464144 | TGTCTGTGTCCTCAC[A/G]TTACCTCACTTAATT | 11124 |
rs75399333 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50564965 | TATTTGTTTTTTTTT[A/T]ATTACTTGCTTTTTA | 11124 |
rs75442667 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | FAF1 | GRCh38.p7 | 1:50446181 | AGCTTAGAGAGGTCA[A/T]GTGACTTAGCTGAGG | 11124 |
rs75448946 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947704 | TCTTATTGAGCCCCT[C/G]AATAAAAGCTAAACA | 11124 |
rs75450883 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50913093 | CTGTCACTTATTATA[A/G]CACTTACTACACAGT | 11124 |
rs75456048 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50477839 | TGCTCAATATGCACT[C/T]GGAAGGGAAGGAATA | 11124 |
rs75482411 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50697831 | GGAGTACATTGAGGG[C/T]AATAAGGTACTATAC | 11124 |
rs75484477 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50870404 | ACAAGTTGCAGAGAG[C/T]CGAGATTGCGCCACT | 11124 |
rs75504300 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50734735 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAAGA | 11124 |
rs75504961 | snp | C/T | 0.282632 | 0.247861 | intron-variant | FAF1 | GRCh38.p7 | 1:50902373 | AGAAATTAAAGAAAA[C/T]ATTTCATTAATAATT | 11124 |
rs75505376 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50796346 | ATGTTAGCTTCTAGC[C/T]TTTTTTTTACGGCAC | 11124 |
rs75520406 | snp | C/G | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50530504 | GTTGGGAAGGGTGGT[C/G]GGGGGAGGTGGGGAT | 11124 |
rs75525604 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | FAF1 | GRCh38.p7 | 1:50694012 | CATTATATATATACA[C/T]GACATATATGACATA | 11124 |
rs75545886 | snp | C/G | 0.122411 | 0.214991 | intron-variant | FAF1 | GRCh38.p7 | 1:50779991 | ATGCACAGACAGACA[C/G]ACACACACACACACA | 11124 |
rs75551582 | in-del | -/GGA | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50600025 | AGATTTTCAGATTAC[-/GGA]GGATACTCAACCTGT | 11124 |
rs75578370 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50698378 | TATTTTAATACTGAA[A/G]AAGAAAAACCTCTTC | 11124 |
rs75580261 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAF1 | GRCh38.p7 | 1:50612021 | ACACATATTGGTGAA[C/T]GAAAACAGTTCGATG | 11124 |
rs75587670 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50528703 | TAAGTCCACTTACAT[A/G]GAGAGTTTTTTCAAT | 11124 |
rs75599831 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FAF1 | GRCh38.p7 | 1:50808241 | CCACTAGACCTGACT[C/T]ACCAGAACTCCTTAA | 11124 |
rs75642970 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | FAF1 | GRCh38.p7 | 1:50441663 | CTTAGTTGATCTTCA[A/G]AATAACCTGCAAGGC | 11124 |
rs75651063 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50869115 | AAAATTGATTCTCCC[A/G]CGATTATGTTTCTTT | 11124 |
rs75651163 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50709604 | GGAACTAATTGTCCC[C/T]GGTCATCAAGCTACA | 11124 |
rs75653435 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50553201 | AGACCAGTGATACTT[C/G]AACAAATAAATAGGA | 11124 |
rs75665280 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50608860 | TGTATGACTCTGGAC[A/G]ACTCTCTCACCTTCT | 11124 |
rs75685970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866736 | CATGGATGGGTAGAA[A/T]CAATACTAGAAAGAT | 11124 |
rs75691618 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50921432 | TAAGGAGGTCCTACA[C/T]CTGGAAGTGAAAGAA | 11124 |
rs75725792 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50721183 | AAATTTTTTTTTTTT[C/T]TTTTGAGAGGAGTCT | 11124 |
rs75730547 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50912049 | CTCAAAAAAAAAAAA[A/G]GGCAGAGTATTTAGA | 11124 |
rs75775178 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50594316 | TGAGATCCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs75777152 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50534298 | TGCTGATAATTTTTT[G/T]GAGACATATTCTCAC | 11124 |
rs75781943 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50850142 | GAAAAAAAAAAAAAA[A/T]TTGAATGGTCAACAA | 11124 |
rs75782433 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50785133 | GCAAGACCCTATCTC[A/C]AAAAAAAAAAAAAAA | 11124 |
rs75791117 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846256 | CATACAAAAAAAAAA[-/AA]GAAAAGAAAAAGTAC | 11124 |
rs75796439 | snp | A/G | 0.100231 | 0.200173 | intron-variant | FAF1 | GRCh38.p7 | 1:50818433 | AAAATGTCTACCAAA[A/G]ACCAGTATACAAATA | 11124 |
rs75839338 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463836 | AAGGCTCAGGCCCAA[A/C]TGTTCTTAAAACTAG | 11124 |
rs75843566 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50451988 | TGGTATCCTTGATGG[C/T]GGCTTTGGTCACTAT | 11124 |
rs75861605 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50720016 | TTTTTTTTTTTTTTT[C/T]TTTGAGAAGGAGTCT | 11124 |
rs75876848 | snp | A/G | 0.281841 | 0.247964 | intron-variant | FAF1 | GRCh38.p7 | 1:50736991 | AAGAAGTAAACCCTA[A/G]CTTTTAAGTTATGTG | 11124 |
rs75880632 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50793065 | CAAAATTAAAGGTCA[C/G]TCTACTAAAATACTA | 11124 |
rs75881270 | snp | C/T | 0.00954224 | 0.0684493 | intron-variant | FAF1 | GRCh38.p7 | 1:50849854 | ATTAAAGGTATCATA[C/T]AATGCATTTCCCCTG | 11124 |
rs75895653 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50661192 | AAAAAACACTAATAT[C/T]TTCCCCTTATGAGAT | 11124 |
rs75896234 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961648 | TAACTAGTGAAATCA[G/T]CATGTAGCATGAAGG | 11124 |
rs75900179 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50549193 | TTGTAAGATAACGTC[C/T]TACTCAGAGCAGAGA | 11124 |
rs75922269 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527869 | TCTCTCCCTCTCTCC[C/T]TCTCTCTCTCTCTCT | 11124 |
rs75926355 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | FAF1 | GRCh38.p7 | 1:50784161 | ACCACTTCTATTCAA[C/T]GTAGTACTGGAAAGC | 11124 |
rs75930273 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50854108 | ATTCAATTAATGCAG[A/T]GTGTTTACCACTATA | 11124 |
rs75937768 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50667034 | TACTTTTAAGTGCTG[C/T]AGAGGAAGAACAACT | 11124 |
rs75947091 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50672700 | AGACTATTGATAAAC[G/T]AGATACTTACATGCT | 11124 |
rs75957150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50904785 | GAACTGCCAGTTTCC[A/G]CAAACCTCCTGAAAC | 11124 |
rs75958505 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50698721 | TTGGGAATTCTCCTT[A/G]TATCCCTCCTCACCC | 11124 |
rs75966686 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50816220 | CTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTT | 11124 |
rs75971201 | snp | A/T | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50779061 | AACCATGTTTATGCA[A/T]AGCGTCTTCATCAGC | 11124 |
rs75990236 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602179 | TTTACTGTTTTTATC[A/T]TTTATTCACTCAGTT | 11124 |
rs76014525 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50615386 | GGGAGGGGCTGTATA[C/T]ACCCGTAATGGAACT | 11124 |
rs76023676 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50749599 | GAGACCAACATGAGC[A/G]ACACAGCAAGACACC | 11124 |
rs76027421 | snp | A/C | 0.305436 | 0.243776 | intron-variant | FAF1 | GRCh38.p7 | 1:50501888 | CCATATTACCATATG[A/C]CTATATAAAATGTGT | 11124 |
rs76028324 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50773455 | TAGATGAACAGATAC[A/C]AAAATGTGGTATATA | 11124 |
rs76041186 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50687744 | AGACTCCATTTCAAA[A/G]AAAAAAAAAAAAGGA | 11124 |
rs76048034 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAF1 | GRCh38.p7 | 1:50538450 | AGAATATGACTACTA[C/T]TGCAGTTTTGTGTTA | 11124 |
rs76052322 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50502842 | TCTAATTTAAAGAAA[C/G]AGGGTCTCACTCTGT | 11124 |
rs76069358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50835384 | TTGTAAAGAATGCAG[A/G]CTTTAGAAAGTTTAA | 11124 |
rs76097312 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50547252 | AATGCACATATTGTA[A/G]GCATGTTGGAGAACA | 11124 |
rs76098868 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50656346 | CCCTACCACCGACCA[A/C]AAAAAAAAAAAAAAG | 11124 |
rs76102742 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50541956 | ATAACAAAACTTTCA[C/G]CACTATACAAAGCAT | 11124 |
rs76104736 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50946677 | AAGACATTGACTCCC[A/C]GGTCAGAGACAATGA | 11124 |
rs76125309 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50591770 | TCACCTCATCTCTTA[C/T]CTTCCTTTTCCCCCG | 11124 |
rs76149275 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50606075 | ATGTAGCATAGTGGA[C/T]TAGATTTTCAACTTT | 11124 |
rs76176490 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50517793 | CTTTTCTATAAAATG[A/G]GTATAATAAAACCTG | 11124 |
rs76179493 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50614033 | ACCTGAGAGGTGGAG[A/G]TTGCAGTGAGTCGGG | 11124 |
rs76183105 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | FAF1 | GRCh38.p7 | 1:50948292 | ATAAAAAAAATCTGA[A/G]GCTGGGTAATTTATA | 11124 |
rs76183578 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50860292 | CTTCTGCACAGCAAA[A/C]GAAACTATCAACAGG | 11124 |
rs76195937 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50797910 | TTAGTTCTAAAACTT[A/C]AACCAAATAAGTGTT | 11124 |
rs76201941 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50541904 | AAGATAAAATAATTA[C/T]GAAAATGTAGATATC | 11124 |
rs76202790 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50536412 | CCAAGGCTTGAGAAG[A/G]GATCTTCTTCTCCAT | 11124 |
rs76205049 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | FAF1 | GRCh38.p7 | 1:50889671 | TCCATGTAGTTGAGC[A/G]GTTTTGAGTGAGTTT | 11124 |
rs76215192 | snp | A/C | 0.279991 | 0.248195 | intron-variant | FAF1 | GRCh38.p7 | 1:50892624 | TTTAGGATACTTTAT[A/C]TTTGATCTCTGGGAG | 11124 |
rs76238724 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50798087 | AAAAAAAAAAAAAAA[C/T]TCCGCATTTATTTTA | 11124 |
rs76244754 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50609886 | AACTTATGTTGCAAA[A/G]CCACGTTTCACCTGT | 11124 |
rs76255042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919908 | GAAGTATAGCAAAGA[G/T]GAGATCTGCTGGTTT | 11124 |
rs76268687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694018 | ATATATACATGACAT[A/G]TATGACATATATATG | 11124 |
rs76272233 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50563990 | AATTTGTTAGAGAAA[C/T]TAGGAAATTTAATTT | 11124 |
rs76280875 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50622165 | GCGAGACTCCATCTC[A/C]AAAAAAAAAAAATAA | 11124 |
rs76288021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50796084 | CAAAAACAAAAAAAA[A/C]CCCTGACCATTTGAG | 11124 |
rs76293293 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50851464 | CTAAATTGGTTTTCC[C/T]GCTGTGAGCTGAATC | 11124 |
rs76296489 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714362 | TAAAAAAAAAAAAAA[-/AA]TTAGCTAGGTGTGGT | 11124 |
rs76331537 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50919466 | AAGAATAAAATAAAG[C/G]CTGCCGGGGGGTAAA | 11124 |
rs76338813 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50958906 | CTAAAATAATTCCTT[C/G]ACCAAACATCAAAAG | 11124 |
rs76361776 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50844464 | TAATATATTGCTTGA[A/G]GCAGACACTATCAAT | 11124 |
rs76363306 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50687401 | AATGGGCAAAGGATT[A/T]GCATAGACATTCCTC | 11124 |
rs76363742 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50897980 | CAATCTGTTCCATCC[A/C]ACCAGATCTGCAACT | 11124 |
rs76364569 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681674 | CAGCCTGTAATCCCT[A/T]TTTTTTTTTTTTTTT | 11124 |
rs76388126 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50898403 | CTATACCTATACAGA[C/T]AGACACATTAAATAT | 11124 |
rs76393990 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50825672 | AACACAAAAAAAACC[C/T]GACATAATAACAAAG | 11124 |
rs76394593 | snp | C/G | 0.148326 | 0.228391 | intron-variant | FAF1 | GRCh38.p7 | 1:50651064 | ACTTCACTGAGTAAC[C/G]TGAAAATGCCCAAGA | 11124 |
rs76425467 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50644456 | ACCCTATGCATGCAC[-/A]GAGACTGGTATTCAG | 11124 |
rs76440979 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50904864 | AGCCATCTGAATAAT[A/G]TTTCCTATTTTTTTC | 11124 |
rs76449429 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50958678 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAT | 11124 |
rs76452583 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50915959 | CATACACTGACACTT[C/G]GATGTTCCCAAAGAA | 11124 |
rs76455335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502511 | TTCCGAGTGAATTAG[A/G]TAAAAGTACAGTATT | 11124 |
rs76508122 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50682183 | AAGGATGTACCTCTA[C/G]AGATAGAGGGTACTT | 11124 |
rs76511280 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50871463 | CATTAGGGGCTAATG[C/T]AGATGGTGACTTTCA | 11124 |
rs76512273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50720978 | ATTTGATCATTCTTC[A/G]AGTCTCATATTTTGT | 11124 |
rs76522845 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50681677 | CCTGTAATCCCTATT[A/T]TTTTTTTTTTTTGTA | 11124 |
rs76529744 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50860315 | TCAACAGGGTAAACA[G/T]ACAACCTACAGAATA | 11124 |
rs76566467 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50727532 | GGTAGGGATACAACA[C/G]TGAACAACAAAAAAT | 11124 |
rs76577325 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50516289 | CCTAGCCTATCCTCA[G/T]CTCTTATTCTTCTGA | 11124 |
rs76579246 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592954 | AAAAAAAAAAAAAAG[A/G]AAGAAAGATGATTGT | 11124 |
rs76581323 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50723400 | GCAAGACTGTCTCCA[A/C]AAAAAAAAAAAAAAT | 11124 |
rs76582550 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50671747 | ATTTTTTTTTTTTTT[G/T]GAGACAGAATCTTAC | 11124 |
rs76583893 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50776690 | AAAACAAAAAAAAAA[A/T]TCTGAGGTAATTTTA | 11124 |
rs76589723 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50742902 | TGGCCTGTGAGTTAA[A/G]AATGGTTTTCACTTT | 11124 |
rs76595394 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50607564 | CTTCTGCTCAGTCCA[C/T]TACTCTTGCCTGGGT | 11124 |
rs76603344 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50770769 | AAGCTCTTTTTTTGT[G/T]CCATATGAATTTTAT | 11124 |
rs76606504 | snp | A/C | 0.280785 | 0.248097 | intron-variant | FAF1 | GRCh38.p7 | 1:50725902 | AGAGGCCACAGAAGA[A/C]AGTGATATGCTTGAC | 11124 |
rs76643295 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592934 | CAGAGCAAGACTCTG[G/T]TTCAAAAAAAAAAAA | 11124 |
rs76660036 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50452913 | TCACCCAACACCACA[G/T]GGTCTCTTAATAGAC | 11124 |
rs76677454 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50516499 | AATTTTTCTTGGACC[A/G]AAATACCAAGCACGC | 11124 |
rs76695769 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50629738 | TAACATCTACCCTTC[A/G]GGATTGATTAACGTG | 11124 |
rs76725784 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960560 | TACACACCACCCTCA[C/G]AAACCAACTAAACAC | 11124 |
rs76736434 | snp | G/T | | | missense | FAF1 | GRCh38.p7 | 1:50491795 | TTTCTCTGGCTTCAC[G/T]TTCATCCTTAAAGAA | 11124 |
rs76743923 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50684550 | AACCAATGATATACC[A/G]GTAAATGGCTCTCCC | 11124 |
rs76753090 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50560608 | ACACTTAGTAGCATG[C/T]ACACTGATGTGCAAA | 11124 |
rs76776990 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50779978 | ACTACAAGCACACAT[A/G]CACAGACAGACAGAC | 11124 |
rs76789762 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463699 | TGGAACAGAACATTA[A/G]TAATTGTTAATTCCT | 11124 |
rs76797724 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50956010 | GATATAAGGACTTAT[C/T]GTTAAATAAGTACGG | 11124 |
rs76852690 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713262 | CAGTTAAAAAAAAAA[-/AA]GGCATGTTTTCTTTT | 11124 |
rs76852824 | snp | C/T | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50655854 | ACGATTATACATTTT[C/T]ATAATTTATTTAATC | 11124 |
rs76868648 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50722214 | GCCAAAAAGCACTGT[C/T]TCTAGTTTACTTCAT | 11124 |
rs76889314 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527846 | CTCTCTCTCTCTCCC[C/T]CTCTCCCTCTCTCCC | 11124 |
rs76893666 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50527251 | GAGTAATAATGTTGA[A/G]CTTCTTTTCATGTGC | 11124 |
rs76894818 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50721182 | GAAATTTTTTTTTTT[C/T]CTTTTGAGAGGAGTC | 11124 |
rs76908108 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50636529 | CAGCTAGGACTACTA[C/T]ACTTTTAGTAGAGAG | 11124 |
rs76910477 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50918203 | TTAATTTTTTTTTTT[A/T]AATTATACTCTAAGT | 11124 |
rs76932415 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50649555 | CTGAATCCTAACACA[C/T]GCCCAAAGAGCTTTG | 11124 |
rs76943844 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50814309 | TAAGTATGCATATTA[A/G]TGTATGCTATATTGC | 11124 |
rs76950216 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50599888 | ACTTAGAACTGTTTT[C/G]GGTTTTGGAATATTG | 11124 |
rs76961778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50950997 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGACCAC | 11124 |
rs76966886 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766791 | AAACAAGCAAGCAAG[A/C]AAAAAAAAAAAAAAA | 11124 |
rs76967973 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50518889 | ACTTTGTATTCTTGA[C/T]GGCAGTGAATAATAG | 11124 |
rs76975671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50660513 | TTCTTTTTTTTTTTT[C/T]CCCAAGACAGTCTTG | 11124 |
rs77009490 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50722665 | AAAAAAAAAAAAAAA[A/G]CCCTATAAAATCTAA | 11124 |
rs77017890 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50521509 | CTCTTGAGAAGGCTT[C/T]AGAAGGTTTCAATTT | 11124 |
rs77024124 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50622767 | ATGACCTCCTCTTTA[C/G]TAAAGTGGGATATCC | 11124 |
rs77026666 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50862918 | GAGATGATGGCAACA[A/C]AGTAATAGCAGGAGA | 11124 |
rs77036096 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50873891 | AAATCTTGGGTCTCG[A/C]ATACCCTGCATCATT | 11124 |
rs77036920 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | FAF1 | GRCh38.p7 | 1:50500408 | AGAGGCAATGTAGTG[A/G]AAAAAGGAAAACCTT | 11124 |
rs77040629 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50543757 | CCAACACTGTCACTG[G/T]TTTTTTTTTTCCATT | 11124 |
rs77056380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549189 | ATCATTGTAAGATAA[C/T]GTCCTACTCAGAGCA | 11124 |
rs77059525 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50661647 | TTATCAGATGTTCTG[A/G]TTAAGAGTTTGTTAA | 11124 |
rs77082692 | snp | C/T | 0.279726 | 0.248226 | intron-variant | FAF1 | GRCh38.p7 | 1:50804875 | GCCAAGCACTACGCA[C/T]TACTTTGTGGATAGC | 11124 |
rs77104022 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50784645 | CAATGCAATCTCTAT[A/C]AAAAGCCCAATGGTA | 11124 |
rs77105681 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50624165 | TTCGAACTTTTTTTT[C/T]CAGATGCAGTCTATC | 11124 |
rs77124941 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50754521 | GTAAATCTGATTCCT[C/G]TTATTCCATACTGGC | 11124 |
rs77128673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50675554 | GATTTTCTGATTCTT[C/T]GCAAGAAGCCAGAAG | 11124 |
rs77132924 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50556243 | ACTCCATCTCCAAAA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs77141271 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50927281 | CCAGAATTTTTTTTT[A/T]AAAGCTTACTGCATG | 11124 |
rs77150187 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50718789 | TTTTTTCTCTCTTTT[G/T]TCTCTTTAGGAATAC | 11124 |
rs77154528 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50772487 | GATGAAGAAAATATC[A/G]TACATTTACACCATG | 11124 |
rs77175241 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50779987 | ACACATGCACAGACA[C/G]ACAGACACACACACA | 11124 |
rs77177523 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | FAF1 | GRCh38.p7 | 1:50729400 | AAGTGAAATGTACCC[A/G]TATTTTTTCTTTTAT | 11124 |
rs77186122 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | FAF1 | GRCh38.p7 | 1:50478867 | TTGTAATTGTTTTAA[A/G]GTTTTTATTAAAGTA | 11124 |
rs77191068 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50895140 | AAATCTTTAACCAGA[C/T]TAAATAAAAGAGGAA | 11124 |
rs77203548 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50728791 | GCCAGACTCCGTCTC[A/C]AAAAAAAAAAAAAGA | 11124 |
rs77206138 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50708486 | TCAAAGTTTGAGATG[C/T]CCATTGAGATGTTTT | 11124 |
rs77209555 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50793547 | GGTAACTGGTAGATA[G/T]TCCATATTGCTTTCC | 11124 |
rs77222361 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50576228 | CAAAACAACCTCTAT[A/G]AAGTAAATACTATCA | 11124 |
rs77236920 | snp | C/G | 0.282105 | 0.24793 | intron-variant | FAF1 | GRCh38.p7 | 1:50637146 | TGTTCTTTTTGAAAA[C/G]TATTTTAGGCTGGGC | 11124 |
rs77256302 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50825033 | GTAATTTCTAGTATT[C/G]AATAACACAACAGAG | 11124 |
rs77256946 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50849723 | TAAGTAAAACATAAT[A/C]AATATCCTTGTAAAA | 11124 |
rs77270042 | snp | C/G/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50819514 | CACCTGTAATCCCAG[C/G/T]TACTTGAAAGGCTGA | 11124 |
rs77273342 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50782371 | GACACAAAAATGCAC[A/G]TTAGGCTAGGCCTAC | 11124 |
rs77283227 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50701647 | ACGTTAGGTTCAAAT[A/G]CTCAGAATCAGAGTT | 11124 |
rs77288530 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | FAF1 | GRCh38.p7 | 1:50643341 | ATTCTGGTTTTTTTT[G/T]TGTGTGCTACTGTTC | 11124 |
rs77293990 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50809379 | GCTAGACTAATGAAG[-/A]AAAAAAAAGATAAAA | 11124 |
rs77304278 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50583374 | AAAATTACTATCCTA[C/T]ATCCTAGTCCTTTGG | 11124 |
rs77308712 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463411 | TATGCTGAGTCCTGT[A/G]AGTCTTCCCAGGAAA | 11124 |
rs77311965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793838 | GTCCTGAATTGCATA[A/T]GCAGCAAGTATAGGT | 11124 |
rs77320121 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50501583 | GGAGAATGGCATGAA[C/T]CCAAGAGGTGGAGAC | 11124 |
rs77334389 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50928800 | AAAAAAAAAAAAAAA[A/C]AACTAGGGAAGGCTG | 11124 |
rs77335760 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50873196 | TTTTAAGACATAATG[A/C]TACTGCACACTTAAT | 11124 |
rs77339514 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | FAF1 | GRCh38.p7 | 1:50745561 | TGGTAGGGTTCTCAG[A/G]AGATCTGGTTGTTTA | 11124 |
rs77340026 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50445135 | GTGGTTTTTGTTACA[C/T]GGGTATGTTCTTTAA | 11124 |
rs77353808 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50797572 | GGTGTGGTGGCAAGC[A/G]CCTACAGTCCCAGCT | 11124 |
rs77363321 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50615471 | GAGAATGCAGACGAG[C/T]TCAGCCACTGTAGAA | 11124 |
rs77370199 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50956558 | CATGTAATTTTACCA[C/T]ATTCACTTTTGGTGA | 11124 |
rs77371039 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865973 | GATACTAACCAAATC[A/C]AACTGCATATCAAAA | 11124 |
rs77380911 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50728007 | GCAGATGGCCTATCA[C/T]GGGACTTTAGCTTGT | 11124 |
rs77397921 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50834053 | GGCAGGAGGTGACTG[C/G]ATCATGTGAGTGGAT | 11124 |
rs77408134 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | FAF1 | GRCh38.p7 | 1:50959324 | CCATCTCATCATTCT[A/G]CTTTTTTACTCTTCC | 11124 |
rs77428412 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50815045 | ACAATAAAAAGAATT[A/C]AAAGCAGTCTCTTAA | 11124 |
rs77429081 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FAF1 | GRCh38.p7 | 1:50946852 | ACAGCCTAAAGAACC[C/T]AAATCTTTTAGAGTG | 11124 |
rs77429763 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50732011 | TCCATGAGTGCTTTA[C/T]GGGGTTATTAAAATC | 11124 |
rs77460775 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50724369 | CTCTTTGCTAGGACG[A/G]GGGCTAGGAGCACAG | 11124 |
rs77465908 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50677895 | AACAAAACTCTGCCT[A/C]AAAAAAAAAAAAAAA | 11124 |
rs77479973 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50904898 | TTTTTTTTCCTTTTT[G/T]TAATATACTTTAAGT | 11124 |
rs77491013 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50602129 | CTGCATGTGACACAC[C/T]CAGTAACACAAGTGA | 11124 |
rs77491617 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50888621 | AGGCCTTTTCTGCAT[C/T]GATTAGGTTTTTGTC | 11124 |
rs77497550 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50486767 | TGATTTAATAATTTG[C/T]ACACAGAAGGAGATT | 11124 |
rs77537035 | snp | A/G/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50860298 | CACAGCAAAAGAAAC[A/G/T]ATCAACAGGGTAAAC | 11124 |
rs77538408 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50928801 | AAAAAAAAAAAAAAA[A/T]ACTAGGGAAGGCTGG | 11124 |
rs77540857 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50687477 | AAAACTGGCCGGGTG[C/T]GATGGCTCATGCCTG | 11124 |
rs77542636 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | FAF1 | GRCh38.p7 | 1:50450451 | AGTCATTACCCTTCA[C/T]TGCCTCTCAACTTCT | 11124 |
rs77546490 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50515619 | TGAGTAAGCAAATGT[C/T]ATACCTATCAAATTA | 11124 |
rs77549435 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | FAF1 | GRCh38.p7 | 1:50659539 | AATTCCAGTTAAGGA[C/G]AAGTGGCACTTCACA | 11124 |
rs77557054 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50549104 | TCAGATCACTAAACA[A/G]GAAGTTATTCTTTAC | 11124 |
rs77565488 | snp | A/G | 0.105924 | 0.204309 | intron-variant | FAF1 | GRCh38.p7 | 1:50573894 | CCACTTTGGGAGGCC[A/G]AGGCAGTTGGATCAC | 11124 |
rs77573012 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527862 | CTCTCCCTCTCTCCC[C/T]CTCTCCCTCTCTCTC | 11124 |
rs77585984 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50479987 | AAACACTGTTGTAAA[A/G]CAACAACATAAAGGA | 11124 |
rs77596479 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50564723 | AGACAATTTTATTTA[A/G]ATGAATCTGTGATAT | 11124 |
rs77603669 | snp | G/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50958107 | TCAAGACCAGCCTGG[G/T]CAACATGGCAAGGCC | 11124 |
rs77616477 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50814421 | GTTTTGGATATATCA[C/T]ATTGTGTGGGTACAA | 11124 |
rs77635966 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50897060 | ACAACACTATTTACA[A/T]TAGCTCCAATTAAAA | 11124 |
rs77637678 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FAF1 | GRCh38.p7 | 1:50560730 | AATGTTTGATTCTAA[A/G]TGTTCTAGAATTAGA | 11124 |
rs77648138 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50609794 | GAAGTTGAATTATGG[A/G]AAAAAAAAAAAAGTT | 11124 |
rs77657858 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50705191 | GGCCCAAGGCATACC[A/G]ACAAGGTACCTCTTC | 11124 |
rs77682744 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50649788 | CTACTAAAACTACAA[A/C]AAAAAAAAAAAAAGA | 11124 |
rs77685156 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50927656 | TGCTGAAAGGTGAGG[G/T]GTAATTGAATGGAAG | 11124 |
rs77686707 | snp | A/G | 0.131723 | 0.220251 | intron-variant | FAF1 | GRCh38.p7 | 1:50926566 | TTTTCAAAAAGATAA[A/G]AAAGCAGACTTTAAA | 11124 |
rs77701130 | snp | C/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50766956 | GTTCCCCAGCAATAG[C/G]TCTTAACCAGGTTGA | 11124 |
rs77703979 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | FAF1 | GRCh38.p7 | 1:50641889 | ATTATTACAGAATCT[C/T]TTTTTTTAGTCCTGA | 11124 |
rs77732134 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50942483 | GGAGGGGAAAGGGAA[A/G]GGAAGGGAATTAAAT | 11124 |
rs77733062 | snp | A/T | 0.281577 | 0.247998 | intron-variant | FAF1 | GRCh38.p7 | 1:50622957 | TAGGACCTGATTCTC[A/T]CCCTCATTATCTTGC | 11124 |
rs77736831 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50927855 | CATTGTTCTTCCTTG[G/T]GTCTCTATGTGCCCT | 11124 |
rs77761089 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50491591 | TGGATAGGATTATAT[C/T]CTTTCTGTTAACTAA | 11124 |
rs77779390 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50648842 | GAGGTAGGAGAATCA[C/G]TTGAACCCAGGAGGC | 11124 |
rs77780148 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50556244 | CTCCATCTCCAAAAA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs77780318 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50687745 | GACTCCATTTCAAAG[A/G]AAAAAAAAAAAGGAA | 11124 |
rs77788102 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464956 | TAGGCATTGGTAACC[C/T]TTACATCCAATCATC | 11124 |
rs77808757 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50929875 | TATTCTGTCTTACCA[A/G]AAGCTACAAATATAA | 11124 |
rs77836738 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656359 | CAAAAAAAAAAAAAA[-/AA]GTAGCACACGTTATT | 11124 |
rs77850159 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50790482 | TCTGCCCTGAGCTTA[A/G]GATTTTATACATAGG | 11124 |
rs77864065 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707294 | TAGACTATACTTAGC[A/G]AGCACCAATATATGT | 11124 |
rs77899630 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50912894 | AAGCCACACCAAAAC[C/T]GAATTCTGATAAACT | 11124 |
rs77904411 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50485938 | CCATCATGAGAACAG[C/T]AAGGGGAAATGGCGC | 11124 |
rs77914551 | snp | C/T | 0.287606 | 0.247155 | intron-variant | FAF1 | GRCh38.p7 | 1:50900353 | TTTGTTTCTCTTCAA[C/T]TATTCTAATCTTTGG | 11124 |
rs77915822 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50634293 | CAGTTTATAATGCTA[C/T]CTTCACAATCTTTCT | 11124 |
rs77932424 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50493754 | CATAAAATACTTATT[A/G]TTTACAGCAACAATT | 11124 |
rs77935192 | snp | A/C | 0.0246293 | 0.108204 | intron-variant | FAF1 | GRCh38.p7 | 1:50715032 | TCTAAAAATATATAT[A/C]TATTTGCATTATCAA | 11124 |
rs77940702 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50497300 | AAAACAACCATCAAC[C/T]CCAGAATTCTATACC | 11124 |
rs77961797 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | FAF1 | GRCh38.p7 | 1:50441344 | GTGACATTGAATTGA[C/G]TGAGACGAGCGTGTG | 11124 |
rs77963966 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50592761 | AAAACCAGTTTGGCC[A/G]ACATGGCAAAATCCT | 11124 |
rs77967615 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50536635 | ACTCACTCAGTAAAT[C/G]AGTTACAGGACAAAT | 11124 |
rs77985870 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50486145 | CTGTTTTCCCACTTA[A/G]TAGTCATTAATATTA | 11124 |
rs77986778 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465001 | CTGCCTGGTGGTATT[C/T]CTATCATCTCATTTT | 11124 |
rs78012880 | snp | A/G | 0.289942 | 0.246789 | intron-variant | FAF1 | GRCh38.p7 | 1:50506343 | TTCCACATACTCTAC[A/G]CTTGACCCAAACAAG | 11124 |
rs78028814 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50570538 | ACACTTAAAAAAAAA[A/T]TTCCCACTTTAAGCT | 11124 |
rs78056587 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50784041 | AGGAAATAACCTCTA[C/T]ATAATAAATGCCATA | 11124 |
rs78068378 | snp | G/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50451250 | ATTAAAGTAAGAGAG[G/T]AATAGAAATTGTGCC | 11124 |
rs78091876 | snp | C/T | 0.127944 | 0.218179 | intron-variant | FAF1 | GRCh38.p7 | 1:50799261 | ACTTGGGCAAGTCTA[C/T]GTAAACTCTCTAACT | 11124 |
rs78096537 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50798458 | CACTAACATTTCTTC[C/T]TAAAAATATCTCCAA | 11124 |
rs78109153 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | FAF1 | GRCh38.p7 | 1:50733582 | GGATTGATGTCCTTA[C/T]AAAAAGATGAAGGGA | 11124 |
rs78111033 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50494743 | TATTTCATATGTCTT[C/T]GTATTTCCTATAGCA | 11124 |
rs78113118 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50745448 | TGTGGCCCTGCTCAA[A/C]TCTCATGTCAAATTG | 11124 |
rs78132573 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50534299 | GCTGATAATTTTTTT[G/T]AGACATATTCTCACT | 11124 |
rs78167265 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50525978 | CACCCAGATGCAAAC[C/G]ACAAACTTTAGGAAA | 11124 |
rs78171786 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | FAF1 | GRCh38.p7 | 1:50640152 | TTTCCCCAATGTCTC[A/G]GACCAATTTTGGTAT | 11124 |
rs78174173 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50484793 | GTTCTGCTTTTATCA[A/G]GCTTATACGTTAGGT | 11124 |
rs78174197 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50487140 | TTAGTATTCACTACA[C/T]TGCACAGCTTCCTCT | 11124 |
rs78176135 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50457491 | TTTAAGTGAGCAAAG[C/T]GTGTCTGCGAAAGCA | 11124 |
rs78183778 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50577110 | TACCAAACTGGTTGT[C/T]GTTTCCTCACTTTAA | 11124 |
rs78204897 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527861 | TCTCTCCCTCTCTCC[C/T]TCTCTCCCTCTCTCT | 11124 |
rs78238512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50794111 | GATACTTTGGTAGGA[C/T]GCATGCATGTTAGGG | 11124 |
rs78239982 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50847420 | ACTATGCCTGAAATT[A/T]AAAAAAAAAAAAAAA | 11124 |
rs78251121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948264 | TACTCTGTTAGTCCA[C/T]TCTTGTGTTGCTATA | 11124 |
rs78278248 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50616394 | CATTGGTAGTTTGAT[C/T]GGAATAACACAGAAT | 11124 |
rs78280022 | snp | A/T | 0.0376468 | 0.132172 | intron-variant | FAF1 | GRCh38.p7 | 1:50580756 | TGTGTTAGAATACTT[A/T]CTCTTTGCTTTTCGG | 11124 |
rs78288854 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50786957 | CAGCTTTGCTTTCCA[A/C]GACTCAATTAATGAA | 11124 |
rs78291486 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50927243 | ATGGCAAAAAGGGTA[A/C]ATTTTATGTTATGTA | 11124 |
rs78291852 | in-del | -/TTTTG | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468474 | ATTTTTTTTTTTTTT[-/TTTTG]AGATGGAGTCTCACT | 11124 |
rs78293456 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | FAF1 | GRCh38.p7 | 1:50675982 | TATTATGTGGTAGAG[C/T]TGAATGTGAATTTGA | 11124 |
rs78318631 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50784310 | CAAAGAAAAAAAAAA[C/T]TTAGAACTAATAAAT | 11124 |
rs78318851 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50849266 | AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAG | 11124 |
rs78323938 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50767645 | AAGCCAGAAGAGATT[G/T]GGGGTTTATATTCAG | 11124 |
rs78325708 | in-del | -/AAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687371 | AAAAAAAAAAAAAAA[-/AAA]CCCAACCTGAAAAAT | 11124 |
rs78345609 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50764756 | TCAAGGGCAAAAGTA[G/T]AAATTCTGTTAATTT | 11124 |
rs78348653 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50795006 | AGGATCTTAATAACA[A/T]AGATAAGAAGACATT | 11124 |
rs78366038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50720015 | CTTTTTTTTTTTTTT[C/T]CTTTGAGAAGGAGTC | 11124 |
rs78366216 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50660501 | AACTAGATTTCTTTC[C/T]TTTTTTTTTTTTCCC | 11124 |
rs78372656 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50722339 | AATGCTCAAAGACAC[A/G]AATAACTTGGAATTA | 11124 |
rs78375373 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50598062 | ACTTTGCAAGGCTGA[C/G]TCAGGAGGATAGCCT | 11124 |
rs78386138 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527845 | TCTCTCTCTCTCTCC[C/T]TCTCTCCCTCTCTCC | 11124 |
rs78389037 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | FAF1 | GRCh38.p7 | 1:50592501 | ATGATCGTAAAGAAA[A/C]TGTGTCTGTAGGGCC | 11124 |
rs78399447 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50779951 | AAGAAAAAAAAGGAA[A/T]CAAAGCATATCACTA | 11124 |
rs78412553 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50479476 | ATTGATCCTCATGCT[A/G]TATGTAATACTGTGA | 11124 |
rs78416402 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592939 | CAAGACTCTGTTTCA[A/C]AAAAAAAAAAAAAGA | 11124 |
rs78419872 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50784309 | CCAAAGAAAAAAAAA[A/C]CTTAGAACTAATAAA | 11124 |
rs78429255 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | FAF1 | GRCh38.p7 | 1:50479763 | CTGCTCCTCAATGTA[C/T]ACAGTCTCCAGGGCT | 11124 |
rs78440468 | snp | C/T | 0.170733 | 0.237101 | intron-variant | FAF1 | GRCh38.p7 | 1:50544597 | CTTCACTGGACCAAG[C/T]GTCTAGTCTCCTGAG | 11124 |
rs78452113 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | FAF1 | GRCh38.p7 | 1:50475164 | GCTACAGATATATCT[C/T]ATTTGAGGAATACAG | 11124 |
rs78461270 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | FAF1 | GRCh38.p7 | 1:50949132 | GCAATTCTCAAGTGT[A/C]GTCCTTGGATCAGAA | 11124 |
rs78461690 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50837673 | TGTACCAAATACATA[A/C]CCAATCTGGAAAGTA | 11124 |
rs78515899 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50699759 | AGCTTTCCTTTGAAT[A/T]TTAAACTGTCAGGGT | 11124 |
rs78520067 | in-del | -/AAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457882 | AAAAAAAAAAAAAAA[-/AAA]GGTAAAAGTTTATTT | 11124 |
rs78523737 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50688669 | AATACAAAATTAGCC[A/G]GGCGTTGTGGCGCAT | 11124 |
rs78526447 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50872956 | CACAGAAACCTCTCA[G/T]GAAAGAAGGCCAACC | 11124 |
rs78553659 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50667828 | AAGCTTCAAACTTTT[A/T]AAAATGCTGACAATG | 11124 |
rs78558089 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50497394 | TTCATCAATAGTATA[C/T]GTATTACAGTAAAAG | 11124 |
rs78565398 | snp | C/T | 0.11963 | 0.213316 | intron-variant | FAF1 | GRCh38.p7 | 1:50877048 | AAATAATTTATGTAG[C/T]TACTCCACCCTCAAG | 11124 |
rs78586429 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50729058 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTG | 11124 |
rs78593246 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50614417 | TAGAGTTAAGGGGGG[A/G]AAAAAAAGAATGTTT | 11124 |
rs78625523 | snp | C/T | 0.279726 | 0.248226 | intron-variant | FAF1 | GRCh38.p7 | 1:50824457 | TCTTTGCATCAACCA[C/T]AGCACTTAAAGTTGA | 11124 |
rs78646566 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FAF1 | GRCh38.p7 | 1:50534700 | TGATATACAACTTCA[C/T]GGGTTATTTTGAGGA | 11124 |
rs78660165 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50750837 | CATGCAGGCCAGGCT[A/G]GTCTCAAACTCCTGA | 11124 |
rs78665920 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50876529 | CGACAAACGAATACG[A/T]CAAAGGGATATAAAG | 11124 |
rs78668697 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648454 | ATATTCAATCATTCA[G/T]TCAACAAATATTTAT | 11124 |
rs78675240 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50785612 | GATGGCTACTATACA[A/C]AAAAAAAAGGAAAGA | 11124 |
rs78731436 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50519759 | CTCCTCCAATCTAAC[C/T]ATCAATTGGAAAAGT | 11124 |
rs78731777 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FAF1 | GRCh38.p7 | 1:50785461 | CCCATTTAAAAAAAT[A/G]GACAAAGGACTTGAA | 11124 |
rs78735799 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50944466 | CTCTGTCCATTGCTA[C/T]AAAATCAGTATGTCC | 11124 |
rs78738909 | snp | G/T | 0.360842 | 0.224085 | intron-variant | FAF1 | GRCh38.p7 | 1:50851702 | AAACAGATGTTTCTT[G/T]CATGCAATAAAGTAA | 11124 |
rs78755251 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50935796 | CTTAAAGCTAACACA[C/T]AGAAGTAATTATGAA | 11124 |
rs78758501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652397 | GCACTATTTTACAGG[A/C]AGAAGAATTGATCAT | 11124 |
rs78770042 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50739574 | CTTTTTCACTGAAGA[A/G]GTATATCCTTGCAAA | 11124 |
rs78770291 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922511 | GAAGAGAAGAGAAGA[A/G]AAGAAAAGAAAACCA | 11124 |
rs78776240 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50916995 | TTCTGCCAGATGAAT[C/T]GTGATAACTACAATG | 11124 |
rs78776673 | in-del | -/CTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556561 | GAAAATTGGCCAGGC[-/CTC]AGAGTGGCTTATGCC | 11124 |
rs78781302 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50625606 | GGAGGGTAGGCGGAG[G/T]GTAAGCACCTTAGAA | 11124 |
rs78781836 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50557035 | AAATTATTTGAGAGC[A/T]GCTCAGAGAATCCAG | 11124 |
rs78802074 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50668609 | CAATTTAATTAAATC[A/G]TATCAAATGAATTGA | 11124 |
rs78803013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50609410 | ATTTATTTGAGGCAA[G/T]GTCTCACTCTGTCAC | 11124 |
rs78808800 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50606493 | TGTGAGAGTTGCTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs78815440 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50671748 | TTTTTTTTTTTTTTT[G/T]AGACAGAATCTTACT | 11124 |
rs78819510 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50570937 | AATCAGAAAACTGCT[C/T]TCGTGAAGAAAGCAG | 11124 |
rs78844493 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50831731 | TTTGCAGATGGAATT[A/C]AAGTAAGGATTGGGA | 11124 |
rs78848190 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50764378 | GTGTAGAGATTACTA[C/T]TCAGCCAAAGATTTG | 11124 |
rs78848672 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50559264 | TCAAAAAAAAAAAAA[A/G]GGATAATCTGTTTTA | 11124 |
rs78863286 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50443675 | GTAAAATGGGAATCA[G/T]AGTTTCTCCTTCATA | 11124 |
rs78877224 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50680201 | TTATGAAACTAGGGT[G/T]TGACTGTTATTGACA | 11124 |
rs78880263 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50786752 | CCATTATGGCATAGG[C/T]ATAGTGAACTAGGAG | 11124 |
rs78882667 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50871154 | GCTTACATTCTACGA[C/G]ACAGGTGAGGACACG | 11124 |
rs78884406 | snp | A/G | 0.126909 | 0.217598 | intron-variant | FAF1 | GRCh38.p7 | 1:50695591 | ATCTATAAAATGGAG[A/G]GCCCATCTCTTTTAT | 11124 |
rs78885842 | snp | A/T | 0.292523 | 0.246357 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460550 | TGAACCAACAGTATA[A/T]ATTAATGTGTCTTTA | 11124 |
rs78888589 | snp | A/G | 0.0283406 | 0.115616 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961623 | CTGATTTTATCCTGT[A/G]GAGCTAAAATAACTA | 11124 |
rs78905899 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | FAF1 | GRCh38.p7 | 1:50958871 | TCTAAGTTGATGCCA[A/C]AATGGCCAAAAATAT | 11124 |
rs78918002 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50610707 | TTTTCTGCTGTTTTT[C/T]TCGGTTAGAAGTTCA | 11124 |
rs78921300 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50896540 | CTAAGTGTCCATGAA[A/T]GGATGTTAAATGGAT | 11124 |
rs78934708 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50861812 | TAATTAAAAAAAAAA[A/T]TTCTGTCTCCCTCAC | 11124 |
rs78941889 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50530269 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATGTATAT | 11124 |
rs78951300 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50668003 | TTTCTCTGAGATGTG[A/G]AAAAAGTGGTGGGAA | 11124 |
rs78953427 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50722662 | AAAAAAAAAAAAAAA[A/G]AAGCCCTATAAAATC | 11124 |
rs78955573 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50849119 | CACACAAAAAAAAAT[A/T]ATCCAGGAGTGGTGG | 11124 |
rs78975044 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50597146 | TGCCTAGCACACAGT[G/T]GGTGGCTCAACAAAC | 11124 |
rs78987324 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683945 | CAAAAAAAAAAAAAA[-/AA]GTAATATTTTAAGGC | 11124 |
rs79006962 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50785611 | GGATGGCTACTATAC[A/C]AAAAAAAAAGGAAAG | 11124 |
rs79025069 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470396 | AGTGCTTAATTTTAC[C/T]TCCCTTGATTCTCCC | 11124 |
rs79033039 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50659886 | ATATAAATCAGGTTA[A/T]TTTTTAATAGTATAG | 11124 |
rs79051005 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592937 | AGCAAGACTCTGTTT[A/C]AAAAAAAAAAAAAAA | 11124 |
rs79059619 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687755 | CAAAGAAAAAAAAAA[-/AA]GGAAATGATGCTCAA | 11124 |
rs79065881 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50799424 | TTTATGGTTACATTA[A/C]AAATCATATACCCTC | 11124 |
rs79070772 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50676696 | GCATGGTGGCAGGTG[C/T]CTGTGATCTTAGCTA | 11124 |
rs79080477 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50454716 | TTTTGCTAAAACAGC[A/G]TTCTTATACTTTGAC | 11124 |
rs79090772 | snp | C/T | 0.173643 | 0.238054 | intron-variant | FAF1 | GRCh38.p7 | 1:50743476 | TGGATTACAGGGGCG[C/T]GCCACCACGCCCAGC | 11124 |
rs79113074 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526272 | GGTGGCATGAGCCAC[A/C/T]GTGCCTGGCCAAAAC | 11124 |
rs79122207 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50592940 | AAGACTCTGTTTCAA[A/C]AAAAAAAAAAAAGAA | 11124 |
rs79132042 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50941231 | TGTTTTTGGAGACAA[A/G]GGCTCACTCACTCTG | 11124 |
rs79132588 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50471129 | AATGAGAGAATACAT[A/G]AATTAAATGCGAATT | 11124 |
rs79136802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645105 | TTTGCAAAAGACTCT[A/G]TATGTTGACAAGGGC | 11124 |
rs79137237 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692610 | AAATGACAGAAGTTT[C/T]TTCTTTTTAAAGGCT | 11124 |
rs79157851 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50605371 | GCATTAAGTTACACA[A/T]TAAGAAATACAACCC | 11124 |
rs79161860 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50559250 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAG | 11124 |
rs79164575 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50923505 | TTCTACAAAACTCTT[A/G]AAAAAAACTAGCACC | 11124 |
rs79165799 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50822790 | TTTTTTTTTTTTTTT[G/T]TGAGACGCAGTTTCG | 11124 |
rs79170582 | snp | A/C/T | 0.0414609 | 0.138013 | intron-variant | FAF1 | GRCh38.p7 | 1:50444764 | TCAGTGAAATAGGTA[A/C/T]GATTCTTTCCATTTT | 11124 |
rs79175924 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50667704 | CATTCACTTAGTTAA[C/T]GTCTAGGTCAGAACA | 11124 |
rs79180055 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50611125 | GTGGGCCTCTTTAAA[C/T]TTACTTCATTGTGCT | 11124 |
rs79184820 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FAF1 | GRCh38.p7 | 1:50836288 | CAATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 11124 |
rs79196684 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | FAF1 | GRCh38.p7 | 1:50741158 | AATGCTGGGATGGGA[C/T]CAAATTAGATACAGA | 11124 |
rs79197946 | snp | A/G | 0.0883596 | 0.190715 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461043 | TGACGAGAGGCTCAC[A/G]AGAACTTAACCCTGT | 11124 |
rs79198048 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50540505 | GGTCTTCTAGTTTCA[G/T]ACTTAGCATGAGATA | 11124 |
rs79206010 | snp | C/T | 0.105214 | 0.203807 | intron-variant | FAF1 | GRCh38.p7 | 1:50591580 | CAGGAGACTGAGGCA[C/T]GAGAATAGCTTGCAC | 11124 |
rs79214373 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50779932 | TTAAAAAAAGAAAAA[A/G]AAAAAGAAAAAAAAG | 11124 |
rs79221947 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50727466 | CACTTTACAATATTC[A/G]TTCCACAAACACTTC | 11124 |
rs79242023 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470536 | TAACTCAAATTTGAT[A/G]TCCATCACTGTTCTA | 11124 |
rs79242933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644646 | GGGATCCAGAAGTTG[A/C]CTCCAGGCAGAATTT | 11124 |
rs79248756 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50644933 | TTCATATTTACTGAG[C/T]AAACATTTCCCTTGA | 11124 |
rs79278986 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50444249 | TGGGCCCCATTCAAG[A/G]AGGACATGGAGCATG | 11124 |
rs79295482 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50501662 | CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAGA | 11124 |
rs79296065 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50642222 | AAAAAAAAAAAAAAA[A/T]ATCCTTGTTCTGTAT | 11124 |
rs79299967 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50625179 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCTCC | 11124 |
rs79304286 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50524891 | TTTTGGTCCCATATG[A/T]ATTTTTTTTTTTGAG | 11124 |
rs79307121 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50842337 | ATTATTTCCTTGAAA[C/G]AATAATTAGCTTTTA | 11124 |
rs79318639 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50630828 | TCTAGTGTATCATAT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs79335628 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50486859 | AAATTTCTCTGCTTA[C/T]CAAAAACTCAGTAGA | 11124 |
rs79339491 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50602828 | TTTTTGACATATATA[C/T]ACATACACCCATGAA | 11124 |
rs79349247 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50848899 | ATTAAATGTGATCTT[A/G]AACCAGAAAAAGCAC | 11124 |
rs79360335 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50943262 | GACTCCAAGCAGCAG[A/G]ATGAGGTCAATTTTC | 11124 |
rs79369465 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471420 | ACTGAAGGTCTACTC[C/T]AGGAAAACCATGCTG | 11124 |
rs79371281 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50457153 | GAGGAGGGAAAGTGA[A/G]AAAAAAAAAAAAATG | 11124 |
rs79411249 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50545731 | GATACAATTCCTTCA[G/T]GGGCAATTTGCCAAT | 11124 |
rs79424702 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50705709 | ATTTCCAACCAGAAC[A/C]GATAAGCCCTCTTTA | 11124 |
rs79429122 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50520859 | CAAAAAACCAAAAAA[A/C]TTTAGCTCTTTATTA | 11124 |
rs79463242 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50867190 | AAAACTCAACACAAC[A/G]TGGATCAAAGACTTA | 11124 |
rs79468516 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50954639 | TCCACCTCCCAGGTT[C/T]AAGTGATTCTCCTGC | 11124 |
rs79470955 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50843199 | TTTAATATTGAGGGC[C/T]GTGTGTCACATATGT | 11124 |
rs79479034 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | FAF1 | GRCh38.p7 | 1:50610234 | TATGATCCATATGAT[A/G]ATATGTTCAATACAC | 11124 |
rs79492740 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50785610 | AGGATGGCTACTATA[A/C]AAAAAAAAAAGGAAA | 11124 |
rs79521580 | snp | A/T | 0.280785 | 0.248097 | intron-variant | FAF1 | GRCh38.p7 | 1:50578053 | TTTACTTAGTGATTA[A/T]CTATATACCAGTTGA | 11124 |
rs79531247 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50730065 | GTTCCATGAAAATTT[A/G]TGAAAAATCCTCTGG | 11124 |
rs79543493 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50843091 | AGCAGGTGATGGAAA[C/T]AGAGATGTTATCGAA | 11124 |
rs79556689 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FAF1 | GRCh38.p7 | 1:50779388 | TGCCAAAATCCATCA[A/G]AAGAATCACTACATA | 11124 |
rs79560897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50835137 | AGAACTGGATTATAT[A/G]AAGTGCTTTATTTGC | 11124 |
rs79564522 | snp | G/T | 0.0433465 | 0.140692 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960480 | AAGCAAAGGCCTCAG[G/T]ATAGCGCCTCCCCCT | 11124 |
rs79587238 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50843470 | GTCTATTGTGCTACA[G/T]AACATCAGAACTTAT | 11124 |
rs79589671 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50797399 | ATAAATACCTTTTTT[A/T]AAAAAAGATATTGAT | 11124 |
rs79615139 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472424 | ACACACACACACACA[A/C]ACCCCAAAACCAAGT | 11124 |
rs79635813 | in-del | -/AAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724252 | CAAAAAAAAAAAAAA[-/AAAA]CAACCATATATATAT | 11124 |
rs79637438 | in-del | -/AAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50722645 | AGAGAGCGACAGTCT[-/AAA]CAAAAAAAAAAAAAA | 11124 |
rs79639283 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50602517 | GCTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTCT | 11124 |
rs79643985 | snp | A/C | 0.0879971 | 0.190408 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463917 | CACATTTCCATGTAA[A/C]CCTAGCTGAGAGGAT | 11124 |
rs79645249 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50514405 | TATCTGCTGGTGCTC[A/T]AAAACAGTGAAATAA | 11124 |
rs79649764 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50662505 | GTTGGAGACGGATTT[C/T]GGCCATCCTGAAACA | 11124 |
rs79649808 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50692980 | AAGTCTCTTATCAAT[A/G]TACAATTTGGAAATA | 11124 |
rs79653552 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50585658 | CATGCTTGTCTGTCC[C/T]ATGTTCAATAAATAA | 11124 |
rs79674907 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50673270 | TCAAAAAAAAAAAAG[A/G]AAAGAAAAAAGAAAA | 11124 |
rs79678135 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50825603 | TATATCTACCAGTAA[C/T]TGATAGAGAAGGGGA | 11124 |
rs79679897 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50957367 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 11124 |
rs79692441 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50745504 | CTGATGGGAGGTGAC[A/T]GGATCATAGGGGGCT | 11124 |
rs79695896 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50672710 | TAAACTAGATACTTA[C/T]ATGCTTCACTTCATT | 11124 |
rs79696756 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50949691 | TATTTACAAAAAAAG[A/G]TGGTGGTTTGGCCCT | 11124 |
rs79701974 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50753757 | ATGTCATTATCTGTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs79704976 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50866398 | AAAGAGGAAATCAAA[C/G]TATTGCTGTTCACTG | 11124 |
rs79705475 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50798086 | TAAAAAAAAAAAAAA[A/C]CTCCGCATTTATTTT | 11124 |
rs79710143 | snp | C/T | 0.015176 | 0.0857769 | intron-variant | FAF1 | GRCh38.p7 | 1:50738816 | TTAAAGCAATTTTAA[C/T]AACTGAGTTTTTCAT | 11124 |
rs79718112 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50551336 | ACAGTATATGGTACA[C/T]ATATGGTACACAGCT | 11124 |
rs79734027 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692611 | AATGACAGAAGTTTC[C/T]TCTTTTTAAAGGCTG | 11124 |
rs79735796 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50654986 | CTTTTTTTTTTTTTT[G/T]TGAGATGGAGTTTCG | 11124 |
rs79737368 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50557309 | GTAGATAAACTGTCA[A/T]ACAGCTTTTAAAAAG | 11124 |
rs79737879 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50870480 | AAAAGAAAGAAAAAA[A/T]TAGAGGTTTATGGCA | 11124 |
rs79755378 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50589757 | TATCATTGCCAAATC[C/T]AATGTCATAAAACTT | 11124 |
rs79765023 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50478180 | TCTTTTTTTTTTTTT[G/T]TGAGATGGAGTTTCA | 11124 |
rs79796073 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50520946 | AATCTTTGCTAGGGA[C/T]ACTTTTTGTAAGGAT | 11124 |
rs79799417 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50871408 | GCAAAAGAGAAGTCA[A/G]TGCCTGGCTTCAAAG | 11124 |
rs79811361 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | FAF1 | GRCh38.p7 | 1:50446958 | GAGGCAGAACCAGAA[C/T]CCAGGCCTTCTGCTG | 11124 |
rs79819370 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50505431 | AGAGAATTTTGGGGG[G/T]GTGTGTATGTGAGTG | 11124 |
rs79830255 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50800367 | AAAAATAAAACTGGA[A/G]TGATATTTAGCAGTG | 11124 |
rs79859002 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50896865 | ACGGAGATGGATGAT[A/G]GTGATGGTTGCACAA | 11124 |
rs79869828 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50860303 | CAAAAGAAACTATCA[A/G]CAGGGTAAACATACA | 11124 |
rs79886777 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | FAF1 | GRCh38.p7 | 1:50767954 | ACCTATCAATATAAA[C/T]TTTGAATGTAAATGG | 11124 |
rs79891440 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50513873 | TAGAATGCAGACCTC[A/C]TGATACCTAATATAC | 11124 |
rs79892910 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50553910 | GCAGCTAAAAAAAAA[A/G]GCTATCTTTTGAAGC | 11124 |
rs79893158 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50955084 | TATTTGATAGCAATC[A/G]CAATTATTTGGATAA | 11124 |
rs79921875 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50566839 | CTGCAAATATAAGAT[A/G]AGAAATGTATTTTTG | 11124 |
rs79922538 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50851465 | TAAATTGGTTTTCCC[A/G]CTGTGAGCTGAATCC | 11124 |
rs79931278 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50777745 | GAATTCATTTTAAGA[A/G]AAAAAAAAAAAAAGG | 11124 |
rs79941013 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50554887 | TATCATCTTGTTTTT[C/T]GTATTTCCAGCCTGA | 11124 |
rs79948214 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50856533 | GTACCAAAACACAAA[A/G]AAGATAAGGAAGCAT | 11124 |
rs79950897 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50728324 | AAAATATAAATGCTC[C/T]AAGGTTTAAGCACAC | 11124 |
rs79952613 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50603533 | AGGTAGTTTTAAACC[A/G]AACTGAGTCATGAGG | 11124 |
rs79959512 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50722649 | GAGCGACAGTCTCAA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs79980292 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50682129 | TGTGAGTCACCACAC[G/T]TGGCAGTATTTCAAT | 11124 |
rs79998886 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | FAF1 | GRCh38.p7 | 1:50636514 | CCTCAGCCTCCTGAG[A/C]AGCTAGGACTACTAT | 11124 |
rs80006792 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50451758 | TCTCTGTAGCATATG[C/G]GGACAGAAAAGCCCA | 11124 |
rs80019068 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50848270 | ATATTATGTTCCTGG[C/T]ATATGCAAAAGTAAA | 11124 |
rs80023475 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50938146 | ATATTCTGAGTAAAT[C/G]TCTGGTTAGGCAAGC | 11124 |
rs80034786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50481118 | TTTAAGCTATTACAA[A/G]ATAATCAGAAAGTTA | 11124 |
rs80048136 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50764535 | GGCTCTGCTTACATT[C/T]CCTTTTTCATGGACT | 11124 |
rs80057903 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50629180 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC | 11124 |
rs80074627 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50753204 | TCTTCCCTAGAGAAC[C/T]ACTAATTTGATTTCT | 11124 |
rs80090685 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50818843 | CTCCATCCCCCCACC[A/C]AAAAAAAAAAAGAAA | 11124 |
rs80101607 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865981 | CCAAATCCAACTGCA[A/T]ATCAAAATGAGAATC | 11124 |
rs80104311 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50925580 | TCAGAATGGCTATTA[A/T]CAAAGACAAAAAATT | 11124 |
rs80108500 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50610116 | GATTAAAAAACATTG[A/G]TCAAATCTTCCGTGG | 11124 |
rs80117673 | snp | A/C/G | 0.031825 | 0.122064 | intron-variant | FAF1 | GRCh38.p7 | 1:50808420 | ATTAATATTAACCTC[A/C/G]TATGTAAATGGGTTA | 11124 |
rs80118491 | snp | G/T | 0.444444 | 0.157135 | intron-variant | FAF1 | GRCh38.p7 | 1:50482488 | GAAAGCAGTTTACTG[G/T]TACTTTCATTTCACT | 11124 |
rs80134023 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50739891 | CACCAAATTTCTTTG[A/C]CAGAAAATTCACATA | 11124 |
rs80138357 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50774808 | CACAATACTTCACAT[A/C]AGACACCATTTTATA | 11124 |
rs80149404 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50526292 | CTGGCCAAAACAATT[C/T]TAAAATTATTTATTA | 11124 |
rs80168536 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50524069 | TCTGTTGTTTCCAGA[C/G]TTTTTAATGAATGCC | 11124 |
rs80169810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50631504 | TTTACTTAATAATGG[C/T]CCCAAAGCTCAAGAG | 11124 |
rs80184555 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50879983 | ACAACAACAAAAAGC[A/G]TAAGTCTTGACAAAG | 11124 |
rs80202057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823308 | AGGTGGCAATTACTC[A/G]GTACAAAGAACTGTG | 11124 |
rs80218915 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50671971 | ACCTAATTTTTACAT[A/T]TTTTTTTGTAGAGAA | 11124 |
rs80222300 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50927285 | AATTTTTTTTTTAAA[G/T]CTTACTGCATGGGGA | 11124 |
rs80248927 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527853 | TCTCTCCCTCTCTCC[C/T]TCTCTCCCTCTCTCC | 11124 |
rs80263645 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50534253 | GAGATGATAATGGTT[A/C]CCTTTAGCCTTGGGG | 11124 |
rs80266206 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50622178 | TCAAAAAAAAAAAAA[G/T]AAAAAGAAAAAAAAA | 11124 |
rs80271470 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50637021 | TATGGATCTATTCCT[A/G]AACACTCTATTTTAC | 11124 |
rs80283605 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50826552 | TGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAT | 11124 |
rs80286553 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50746732 | AAGTTTACATAAGTA[A/T]AGAAAAGCCAAGTGC | 11124 |
rs80294865 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50954699 | ACCAGCCACCATGCC[C/T]GGCTAATTTGTGTGT | 11124 |
rs80297338 | snp | A/C | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50790005 | CTCAACCTTTCATAT[A/C]TCAGATTGAATGTTT | 11124 |
rs80299389 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50742840 | AGCAGCGGGGGATAG[A/C]AAACTATGGCCTGTG | 11124 |
rs80312157 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50779970 | AGCATATCACTACAA[A/G]CACACATGCACAGAC | 11124 |
rs80313193 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50530275 | TGTGTGTGTGTGTGT[A/G]TATGTATATATGTAT | 11124 |
rs80314578 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50684277 | TTTTTTTTTTTTTTT[G/T]TGGTTCAAACTCTGA | 11124 |
rs80315981 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50447716 | CATCTTACCTCTTAC[A/G]CCAATGTCAAGGACA | 11124 |
rs80326064 | snp | C/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50775179 | TGCTGGTCACATAAA[C/T]TTTAATGAGTGTACA | 11124 |
rs80336075 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50689291 | AACAAGAGAACTGAA[A/C]ACATATGTCCAGGCC | 11124 |
rs80337531 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50833598 | TATCCCCTGTCCTCT[A/C]CCCAGAGGTTGGGGA | 11124 |
rs80337925 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50718865 | TTTTAAATTAAAAAG[C/T]GTGACACATGGCAAT | 11124 |
rs111229488 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50714727 | AACAGCTATGGACCC[G/T]TGGAAGATGAATCAA | 11124 |
rs111238328 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | FAF1 | GRCh38.p7 | 1:50739271 | ATGTGCATGTGTACA[C/T]GTGCATACATATACA | 11124 |
rs111253797 | in-del | -/T | 0.478354 | 0.101757 | intron-variant | FAF1 | GRCh38.p7 | 1:50750973 | GCTCTTTTTTTTTTT[-/T]AACATGAAATGGGTG | 11124 |
rs111258551 | snp | C/G | 0.18134 | 0.240387 | intron-variant | FAF1 | GRCh38.p7 | 1:50540225 | GATCCACCTGCCTCG[C/G]CCTCCCAAAGTGCTG | 11124 |
rs111266990 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50441651 | GTCTCGCAGTATCTT[A/G]GTTGATCTTCAAAAT | 11124 |
rs111278364 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50767719 | GCCAGATTAAGCTTC[A/G]TAAATGAATCCTTTT | 11124 |
rs111305017 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50598966 | CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAAG | 11124 |
rs111305376 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865374 | AATCATGCTGCTATA[A/C]AGACACATGCACACG | 11124 |
rs111308543 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50692908 | TTGCCAATTTTCAAT[C/T]AGATTATTTGTCTTT | 11124 |
rs111308652 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50866784 | CAATCTGGAACTTCA[A/G]TGCAATTGCCATCAA | 11124 |
rs111313816 | snp | A/G | 0.0298908 | 0.118541 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460697 | GGAGTGTAGTGGTGC[A/G]ATCACAGCTTAATGT | 11124 |
rs111330377 | in-del | -/AGTA | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50443757 | GTGTCTGAGCCAATG[-/AGTA]AGTACTCAGTAGGTT | 11124 |
rs111330709 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50673956 | ATGTGACTCTGAGGC[-/T]TTTTTTTTTTTTGAC | 11124 |
rs111338002 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50821530 | ATAAACTCATATATT[A/G]TTAAATATGCTCAAA | 11124 |
rs111341494 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50646008 | CTTCTAATCTGCAAC[A/C]ATTTTTGTCCCTAAA | 11124 |
rs111345085 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50671125 | ATGTAAGTTTGAAGG[C/G]CGGGCACAGTGGCTC | 11124 |
rs111352324 | snp | C/T | 0.152001 | 0.229992 | intron-variant | FAF1 | GRCh38.p7 | 1:50755008 | AATTCAAGATGAGAT[C/T]TGGGTGGGGACACAG | 11124 |
rs111358652 | snp | A/G | 0.281313 | 0.248031 | intron-variant | FAF1 | GRCh38.p7 | 1:50595103 | CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCACA | 11124 |
rs111368210 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50696117 | ATGGAAGAGGTATTA[C/G]ATGTGTAAGATAGAA | 11124 |
rs111370304 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50539935 | AAGCAGGAAGCATAC[C/T]CTAAATGCTGTCTGG | 11124 |
rs111372167 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50860544 | AAATCAAAACTACAA[C/T]GACATACCATCTCAC | 11124 |
rs111383113 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50664801 | TCCGTCTCAAATAAA[C/T]AAACAAACAAACAAA | 11124 |
rs111389040 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50650325 | TAAAACTGAAAGAGT[C/T]GGCCGGGCACAGTGG | 11124 |
rs111391875 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50922725 | TGTGGGGGCTGAGGC[A/G]GGAGAATCACTTGAA | 11124 |
rs111401993 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50596081 | CAGGTAGGTGGGGGA[C/T]GGGCCTTCTGTTCAA | 11124 |
rs111403858 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50570425 | TCGCCTCGCCCCTCT[C/T]TTCACTGGAAGCTGA | 11124 |
rs111409409 | in-del | -/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50643341 | TTCTGGTTTTTTTTT[-/G]TGTGTGCTACTGTTC | 11124 |
rs111425975 | in-del | -/A | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50930815 | TCCGTCTCAAAAAAG[-/A]AAAAAAAGTAGGTAA | 11124 |
rs111429121 | in-del | -/T | 0.046775 | 0.145601 | intron-variant | FAF1 | GRCh38.p7 | 1:50831136 | TAGACAAAGCAGGGA[-/T]TTTTTTTTTAAAGTT | 11124 |
rs111431869 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50837251 | GTGAGCCACCGTGCC[C/T]GGCCATATGTTATGT | 11124 |
rs111438623 | snp | A/C | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50825948 | AAGAAATTAAAACAA[A/C]TTCCATATTTAAATT | 11124 |
rs111440287 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50813677 | CATGTTGTTGAGGCT[C/T]GTCTCAAATTCCTAG | 11124 |
rs111443958 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50451925 | AACTTGGCACACTGT[C/T]GGGGACACCCTGGGC | 11124 |
rs111445808 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50727663 | TGAAAGTATTGCTCC[C/T]TTGACTGAAAGTGTC | 11124 |
rs111457688 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50941417 | AGATGGGGTTTTACC[A/G]TGTTGGCCAGGCCAG | 11124 |
rs111461848 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50910663 | AGTGAGCAAGGCTCC[A/G]TGGCCGTGGGACCCT | 11124 |
rs111469705 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50668909 | CCTGAAGTCTCCTGT[C/T]AAAAAATTACTCCTA | 11124 |
rs111471142 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50886463 | ACACATGTGCCATGT[G/T]TGTGTGCTGCACCCA | 11124 |
rs111476427 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50443615 | CACTTCCTACCAGTA[C/T]GACTTTGAAGAAATT | 11124 |
rs111481759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50475912 | TTGATGACACATATT[A/G]TTAAATATATAGGAA | 11124 |
rs111483490 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907940 | GTTTGCTCTTGCTTA[G/T]CTAGTTCTTTTAATT | 11124 |
rs111485988 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50899388 | CATATTTTCTAGCTT[A/C]TTACATGCTTGGTAA | 11124 |
rs111493273 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50919505 | TTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCGC | 11124 |
rs111495700 | snp | C/T | 0.081446 | 0.184634 | intron-variant | FAF1 | GRCh38.p7 | 1:50694061 | CATGTATGACATATA[C/T]ATGACATATACATGA | 11124 |
rs111507981 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447383 | GCCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 11124 |
rs111517306 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50590684 | TCAAATAGAAATGGT[-/G]AAAGGGGTCATTCTT | 11124 |
rs111525311 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50687355 | AACGTTTTATCAATC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs111538500 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50764517 | AACTCTGCAGGACCG[C/T]TGGGCTCTGCTTACA | 11124 |
rs111539308 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50745047 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGTGGGC | 11124 |
rs111544782 | snp | A/C | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50911317 | CCTCAAGTGATCTGC[A/C]TGCCTCGGCCTCCCA | 11124 |
rs111546036 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50539028 | ACCAACCCTTGGAGT[A/G]CATTACTAACAGTAA | 11124 |
rs111549412 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50488693 | TTTATAGTCATAAAG[A/T]CCTGGATGAGAATCT | 11124 |
rs111562429 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | FAF1 | GRCh38.p7 | 1:50485131 | ATTATTATTATTATT[A/T]TTTTTTTTAAATAGA | 11124 |
rs111566559 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50950213 | AAAGAACCACAGCTA[A/G]GAAAACCTAAAACAA | 11124 |
rs111567650 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50590282 | TCCAACCCATGTACA[C/T]GAAATGTGTTTCCAT | 11124 |
rs111570226 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50941880 | TTTTATACATACTTT[A/G]TGAAAATGATTTTTA | 11124 |
rs111580012 | snp | A/C | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50731643 | AAAGTGCTGGGATTA[A/C]AGGCATGAGCCACCG | 11124 |
rs111592122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50454623 | GGATCCTCAGACAAG[A/G]CAGTTGCCAAGGTCT | 11124 |
rs111596162 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909345 | GGTGAATCTGACAAT[G/T]ATGTGTCTTGGAGTT | 11124 |
rs111604405 | snp | C/T | 0.281577 | 0.247998 | intron-variant | FAF1 | GRCh38.p7 | 1:50533095 | TGCTAGGATTACAGG[C/T]GTGAGCCACTGTGCT | 11124 |
rs111605271 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50653668 | GTCAGGAGTTCAAGA[C/G]CAGCCTGGCCTACTT | 11124 |
rs111609856 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50618517 | ATCAGGCTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 11124 |
rs111618594 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50624020 | GAAGAAAGAAGAAGA[A/G]GAAAGAAGAAAGAAG | 11124 |
rs111621732 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50949996 | ACACCCAGCTAATTT[-/A]AAAAAAAAAAAATTT | 11124 |
rs111628348 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | FAF1 | GRCh38.p7 | 1:50742337 | AAAAAAGAAGAAGAA[A/C]GAAGTAAATTGAAGT | 11124 |
rs111632161 | snp | C/T | 0.357451 | 0.225731 | intron-variant | FAF1 | GRCh38.p7 | 1:50726148 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 11124 |
rs111634926 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50880647 | TATCATGTGAAACAT[C/T]GATCGTGGACTTCTA | 11124 |
rs111655281 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50807027 | CTAATTCCCCAGTAC[A/T]GGGTCTTAACCAGAC | 11124 |
rs111655515 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50837933 | TATTTTTAGCAGAGA[C/T]GGGGTTTCACCGTGT | 11124 |
rs111669251 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50472915 | AAGAATGAAGGGCCT[G/T]TAACTCTCACCCCAC | 11124 |
rs111669898 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50862105 | CCACAGAAAGCAACG[-/A]AAAAAAAAAACACAT | 11124 |
rs111677187 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50776679 | AAACAAAAAAAAAAA[-/A]TCTGAGGTAATTTTA | 11124 |
rs111682826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50792838 | ATTCCAGAATGGCAG[A/G]GGTCAAATGGCAAAA | 11124 |
rs111684735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50910188 | CAACAGCAGAGGCAG[A/C]AGAAAAGCAAATATT | 11124 |
rs111686512 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50513853 | CCCAGAGTCACATAG[C/T]TTGTTAGAATGCAGA | 11124 |
rs111699227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50481513 | AGCCTAGGAGCAACA[A/G]GTTATACCATATAAT | 11124 |
rs111701702 | snp | C/T | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50818774 | GCCGGGAGGCAGAGC[C/T]TGCAGTGAGCTGAGA | 11124 |
rs111701872 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50783856 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACTCCAT | 11124 |
rs111703977 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50534533 | CTACCTCAGCCTCCC[-/A]AAAGTGCTGGGATTA | 11124 |
rs111708621 | in-del | -/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50683039 | TCCGTCACAAAAAAA[-/G]AAGAAAAAGGAAATC | 11124 |
rs111716111 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50671854 | GCTGTGTCACCCAGA[C/G]TGGAGTGCAGTGGCA | 11124 |
rs111716460 | snp | C/T | 0.000799808 | 0.0199816 | intron-variant | FAF1 | GRCh38.p7 | 1:50452144 | AACATAAAATGAATA[C/T]ACAAAGAACGAGAAC | 11124 |
rs111725115 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50705773 | TATTTCTTAGCTGTG[A/G]GACATAACTCACCTC | 11124 |
rs111728302 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50762764 | TAGGCATTACCATTC[A/G]GGACATAGGCATGGG | 11124 |
rs111731850 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50843046 | GATAAATTCATTTTG[A/G]AATTATTTACTAGCT | 11124 |
rs111732191 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50866714 | ACAAATGGACACATC[A/C]CATGATCATGGATGG | 11124 |
rs111738064 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468145 | GCACAGGAGGCTGGG[A/G]CTGCAGTGAGCTATA | 11124 |
rs111742185 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50631967 | TTATTGTGCCTAATT[A/T]ACAAATTAAACTTTA | 11124 |
rs111748717 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50586258 | TGGTTGATACAGGGA[C/G]AGGTCAATGGGGAGC | 11124 |
rs111752464 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50724312 | ACACACACACACACA[C/T]ACACACACACACACA | 11124 |
rs111760520 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50762914 | GGCAACCTACAAAAT[A/G]GGAGAAAATTTTCAC | 11124 |
rs111776925 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50753921 | CGCCACCATGCTCAG[C/T]TAATTTTTGTATTTT | 11124 |
rs111777270 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50573145 | GAGTGTTGCTCTGTT[A/G]CCCAGGCTGATGGCA | 11124 |
rs111779227 | snp | A/C | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50863315 | AAATTATTTGAACTT[A/C]ACAATAATAATGGCA | 11124 |
rs111788179 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50623965 | AGAAAGAAGAAGAAG[A/G]AGAAAGAAGAAGAGG | 11124 |
rs111790258 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50684939 | GGCCTAAACCAATTA[C/T]ACAAATGAATGTTGT | 11124 |
rs111794640 | in-del | -/AT | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50819705 | TACATATATATATAC[-/AT]ATATATATACGTATA | 11124 |
rs111810191 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50750812 | ATTTTTAGTAGAGAC[A/G]GGGGTTAACCATGCA | 11124 |
rs111810195 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50456248 | CACTGCAGGCTTGTG[C/T]CACCCACAATCTTCT | 11124 |
rs111816289 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50789200 | CAGTATCTTTGACAT[C/G]TCTTTCTCTTCTGGA | 11124 |
rs111823885 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50855109 | CCAAAATCTGAAAAA[A/C]TCCAAAATCTGGACA | 11124 |
rs111825097 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50901930 | TAGAAGTACTATAAG[C/T]AGATCTTTTAGAACA | 11124 |
rs111829380 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50518535 | AAGCTCCGCCTCCCG[A/G]GTTCACGCCATTCTC | 11124 |
rs111830822 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50638609 | CCACCATGCCCAGCT[A/G]ATTTTTTTGTATTTT | 11124 |
rs111832500 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50649561 | CCTAACACACGCCCA[A/G]AGAGCTTTGATTCTA | 11124 |
rs111834174 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50448696 | ACATCAGCAAGCCCC[A/T]TGGCTGCTTAATCTC | 11124 |
rs111834465 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50553465 | TGAACCCCAAATGAT[C/T]TTGTCAATCAACTGC | 11124 |
rs111867300 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50780500 | GTAGAGACAGGGACT[C/T]ACTTTCTCATCCCCT | 11124 |
rs111870125 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50922963 | ATACCAAAGAAACAC[A/G]AAAGATCATTGCAGG | 11124 |
rs111870790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50887300 | CAGATGAGTAGATTG[A/C]AAAAATTTTCTCCCA | 11124 |
rs111872237 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50890016 | AGTCTCTTTGTAGGT[C/G]TCTAAGGACTTGCTT | 11124 |
rs111876956 | snp | C/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50627699 | TAAAGGGAATGTGAG[C/G]GGGGGCTTCTGGGAT | 11124 |
rs111892623 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50554986 | AGAAAACAGTTGTAA[C/T]GAAAAATTGTGGTTT | 11124 |
rs111901479 | snp | A/G | 0.114387 | 0.210022 | intron-variant | FAF1 | GRCh38.p7 | 1:50606715 | CATGTTGGTCAGGCT[A/G]GTCTCGGACTTCTGA | 11124 |
rs111914338 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50796061 | AAAACAACAACAACA[A/C]AAAAAAACAAAAACA | 11124 |
rs111938598 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50724146 | GCTAAGGCAGGAGGA[C/T]GACTGCTTGAGCCCA | 11124 |
rs111940518 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50518168 | CCAGTTCTCTGTCCC[A/T]ACACTTTTACCTTTT | 11124 |
rs111946633 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50573109 | TGAATTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 11124 |
rs111949735 | snp | A/G | 0.280256 | 0.248162 | intron-variant | FAF1 | GRCh38.p7 | 1:50892350 | GTTCACGCTTGGTGC[A/G]CTGCACCCACTGTCC | 11124 |
rs111951410 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50635837 | TGCTCAACTGATAAA[C/T]AGAAATTTAGGTCAG | 11124 |
rs111956235 | snp | A/C | 0 | 0 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468384 | TGCAACCTCCGCCTC[A/C]CAGGTTCAAGCAATT | 11124 |
rs111956492 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50452475 | TCCAGTAAGACACAC[A/G]AACACCATTTTCAAT | 11124 |
rs111963032 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | FAF1 | GRCh38.p7 | 1:50893841 | AAGCCAGACTAGGGT[C/G]AAACACCTTAGAAAC | 11124 |
rs111970654 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50774541 | AAATAGTATCCAATA[C/T]AGTAAAAGTAGCTTT | 11124 |
rs111978716 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50681569 | CTCGAGTGCAATGGC[A/G]CAATCTCGTCTCACT | 11124 |
rs111979165 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50803614 | GAATACAAAGAAAAG[C/T]CACCTATTCAAGACT | 11124 |
rs111991832 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50693757 | TACATTTCACAGCAA[C/T]ATATTTACACATTTA | 11124 |
rs111996074 | snp | G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50590524 | TGAATTCATTTTTTA[G/T]TTCCAATAGTTTTTT | 11124 |
rs111997851 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947190 | ATTCAACCACTACTT[C/T]CCTTAGGGAAAAAGA | 11124 |
rs112028508 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50729765 | TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 11124 |
rs112036959 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50832472 | TAAGTGCCAATAGCA[C/T]CCTCAGAGTACAGTA | 11124 |
rs112038356 | in-del | -/A | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50771965 | TTCTCTTCTAAATGC[-/A]AAAAAAAATTGACAG | 11124 |
rs112043939 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50931594 | AGCACGTGGGTGGGC[A/G]CAGTGACTCACACCT | 11124 |
rs112045565 | snp | C/G | 0.113334 | 0.209338 | intron-variant | FAF1 | GRCh38.p7 | 1:50650446 | CCAACACAGCGAAAC[C/G]CTGTCTCTACTAAAA | 11124 |
rs112049131 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50844622 | GCAGTGTCAACATAA[C/T]GATGGAGCCAAGAAA | 11124 |
rs112070711 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50870386 | CACTTGAACGCGCGA[A/G]GCACAAGTTGCAGAG | 11124 |
rs112090968 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50742100 | GACTGCATGAGTCCA[C/G]GAATTCAGGATCAGT | 11124 |
rs112095647 | snp | C/G | 0.151668 | 0.229849 | intron-variant | FAF1 | GRCh38.p7 | 1:50771630 | AATGGGCCCAGCACA[C/G]TGGCTCACACCTGTA | 11124 |
rs112099269 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50545667 | TTGGCAAGGTTACAG[A/G]AAAACCAGGAAAAAG | 11124 |
rs112104612 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468617 | GGCGCCTGCCACCGC[A/G]CCTGGCTAATTTTTT | 11124 |
rs112108602 | in-del | -/G | 0.218151 | 0.247963 | intron-variant | FAF1 | GRCh38.p7 | 1:50684148 | GCCAAAAACTTAGTA[-/G]GTAGCAAAGTCATAG | 11124 |
rs112109071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50608937 | TGTTGTGAAGATTCA[A/G]GAGTATGTGTATCTG | 11124 |
rs112111914 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460814 | TATTTGTATATGTGT[A/G]TGTGTGTGTGTGTGT | 11124 |
rs112111991 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50585892 | CATAAAAAAAAAAAA[-/G]AAAAAAAAAGAAAAA | 11124 |
rs112112277 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50770447 | GAAAATCAGTACCAT[A/T]TCTACATACCTACAA | 11124 |
rs112112465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591873 | CTGAATGGAATGAAT[A/G]GAATATGATTCCTTT | 11124 |
rs112122866 | in-del | -/TGTG | 0.5 | 0 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460809 | CTAAGTATTTGTATA[-/TGTG]TGTGTGTGTGTGTGT | 11124 |
rs112123418 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50907220 | CAGCCTTGCATCCTA[C/T]GGATGAAGACAACTT | 11124 |
rs112130452 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50756820 | TATAAAATCATCAGA[A/T]CTCATGAGACTTATT | 11124 |
rs112133377 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662699 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTG | 11124 |
rs112134442 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50771819 | GGCAGGGGAATTGCT[C/T]GAACCTGGGAGGCGG | 11124 |
rs112143246 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50892487 | GGCCATCTTGGAACC[A/G]CCTCCCTTCAGCTCT | 11124 |
rs112150027 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50491350 | CTATTCACTTCTCTC[C/T]CCTTCAAAGCTCAAC | 11124 |
rs112150793 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50457472 | ATGGGGTTATTATAC[A/G]GACTTTAAGTGAGCA | 11124 |
rs112164717 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50944357 | GGAAGGCTTCAAGGG[A/C]GATTCTGAAAGAAAA | 11124 |
rs112166930 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50831509 | AAGAATATATCTGCC[A/G]TCTTTCTCTACACCG | 11124 |
rs112173124 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50845920 | CTGAGGTCAGGAGTT[C/T]GAGAACAACCTGGCC | 11124 |
rs112176297 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50926852 | GTTGACAATATCCAA[A/T]ATGTATAAACAACTC | 11124 |
rs112176474 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50759287 | GTATATCTCCTAAAG[C/T]TATCCCTCCCCCCTC | 11124 |
rs112185786 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50642233 | AAAAAATCCTTGTTC[C/T]GTATCTTTTCTGATG | 11124 |
rs112186417 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50736772 | AAAGAAAGAAAGAAA[A/G]AAAAAAGATGTCAAA | 11124 |
rs112190902 | in-del | -/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50744909 | TGAATATTTCTGTAT[-/C]TATAAAATGGGAAAT | 11124 |
rs112192962 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50665160 | GAAATAACTGGAACA[A/G]TTATAGAAACATTTT | 11124 |
rs112195677 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50540836 | CTTTTAATAACACAG[A/G]TCACAAAAGGCAAAA | 11124 |
rs112217847 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50820613 | CAGAATTTATTCATG[C/T]TACAACTGAAAGTTT | 11124 |
rs112218462 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50827328 | TAATCTATAACCTTA[A/C]CCCCAACTCCGTGCC | 11124 |
rs112243606 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50479485 | CATGCTATATGTAAT[A/G]CTGTGATCAACATAT | 11124 |
rs112247206 | snp | C/T | 0.277867 | 0.248442 | intron-variant | FAF1 | GRCh38.p7 | 1:50752120 | GACTACAGGCGCGTG[C/T]CACCACACCCAGCTA | 11124 |
rs112251459 | snp | C/T | 0.067446 | 0.170804 | intron-variant | FAF1 | GRCh38.p7 | 1:50452254 | AGAACAATTTGCAAG[C/T]TCATTGCCCCTGAAA | 11124 |
rs112256187 | snp | A/G | 0.0433465 | 0.140692 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50962082 | GCTTAATTTTCAGCC[A/G]TAAGAAAATAATTCC | 11124 |
rs112259013 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50944055 | AATCTGTCCCATTTG[G/T]CCAGGCCATAAGCCA | 11124 |
rs112279132 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50598036 | TGGTGGCTCATGCCT[A/G]TAATTCCAGCACTTT | 11124 |
rs112282787 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50755734 | ACATCTTCTGAAATA[C/T]AGGCAGAGGTTCCCA | 11124 |
rs112287615 | in-del | -/AA | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50850128 | GGGTTAGGAGCTACG[-/AA]AAAAAAAAAAAAATT | 11124 |
rs112295345 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50650277 | CAACAAGAGCGAAAC[G/T]CTGTCTCAAAAAAAA | 11124 |
rs112299817 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50783643 | CTCTGGGAGGCTGAG[A/G]TGGGCGGATCACTTG | 11124 |
rs112309008 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50821338 | GTGCCAGAAATCATA[A/T]TTTTTTACAGGCTCC | 11124 |
rs112312742 | snp | A/G | 0.131381 | 0.220067 | intron-variant | FAF1 | GRCh38.p7 | 1:50941166 | CTTCCTCAGTAGCTG[A/G]GACTTACAGGTGCGC | 11124 |
rs112324543 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50492740 | TTTTTTGTCTCCCCA[A/G]TATATGCTTACTCAA | 11124 |
rs112331712 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50734594 | AAAAAATTAGCCGGG[C/T]GTATTGGCGGGCGCC | 11124 |
rs112332643 | snp | G/T | 0.0232938 | 0.105441 | intron-variant | FAF1 | GRCh38.p7 | 1:50606721 | GGTCAGGCTGGTCTC[G/T]GACTTCTGACCTCAG | 11124 |
rs112348928 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50446445 | TTTTGGATGTTCTGA[C/T]TTGGGATGCTCAACC | 11124 |
rs112350914 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50515541 | AAAGCACGGTAGTTC[A/C]GACAGCAAACAAAAT | 11124 |
rs112357322 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50618554 | AGGCATGAGCCACCG[C/T]GCCCGGCCACCTAAA | 11124 |
rs112367658 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50686369 | CCAACATGGAGAAAC[C/G]CCGTCCCTACTAAAA | 11124 |
rs112376808 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50624941 | AGTTTTGCTCTTGTT[A/G]CCCAGGCTGGAGTGC | 11124 |
rs112414817 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50742481 | CTCCACCTCCCAGGT[C/T]CAAGCGATTCTTGTG | 11124 |
rs112415808 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50762415 | GAACAAAGCTGGAGG[C/T]ATCACACTACCTGAC | 11124 |
rs112430201 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865849 | ATAATAATAATAAAA[A/G]AAAAAAAAAAAGAAA | 11124 |
rs112430490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50504651 | AAATGGTAACACCCA[A/G]TTTTAAAGAAACTCC | 11124 |
rs112444485 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50828472 | GACGGGGTTTCACTG[C/T]GTTAACCAGGATGTT | 11124 |
rs112445873 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50951149 | TAAGGCAGGAGAACT[A/G]CCTGAACCGGGGAGA | 11124 |
rs112446754 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50706797 | GTGTAATTTTGCCAT[A/G]CCTATGGTACCAGGA | 11124 |
rs112452014 | snp | C/G | 0.120326 | 0.21374 | intron-variant | FAF1 | GRCh38.p7 | 1:50723824 | CCTGATCTTGGCTCA[C/G]TGCAACCTCCGCCTC | 11124 |
rs112455930 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50483169 | GCTTGTGATGCAATA[C/T]ATGAATTGAAGCATT | 11124 |
rs112457318 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50571591 | TATTAAAGATTAAGC[A/G]GCTCCTTCATTTTTC | 11124 |
rs112472180 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50556810 | CCACTGCATTCCAGC[C/G]TGGGCACCAGAGCAA | 11124 |
rs112479181 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50739260 | TGTGTCTATATATGT[A/G]CATGTGTACATGTGC | 11124 |
rs112482299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50454057 | ATGGACCTGCTATGA[A/G]CATCATCACAGCTTA | 11124 |
rs112488983 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50672342 | CACCGCGCCCCAGCC[A/T]GTTTTGTTTTGTTTT | 11124 |
rs112494106 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50519321 | GTGACAGAGCGAGAC[A/T]GTCTCGAAAGAAAGA | 11124 |
rs112500419 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50653937 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 11124 |
rs112507450 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50895630 | CTGATGAACATTGAC[A/G]CAAAAATCCTTAACA | 11124 |
rs112516611 | snp | A/G | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50606625 | CTGCTTCAGCCTCCC[A/G]AGTAGCTGGGATTAT | 11124 |
rs112522393 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50804175 | GAACATAAGACAGCT[G/T]GCCTTCTACGTAGGA | 11124 |
rs112527145 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | FAF1 | GRCh38.p7 | 1:50736483 | GGCTGGGCACAGTGG[C/G]TCACGCCTGTAATCC | 11124 |
rs112527464 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50623407 | ACCCTGTCTCTACTA[A/C]AATACAAAGAAATTA | 11124 |
rs112568731 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50724308 | ACATACACACACACA[C/T]ACACACACACACACA | 11124 |
rs112568996 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50722509 | AAAACATTAGCCAGG[C/T]GTGGCGGCGGGCGCC | 11124 |
rs112573893 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50721130 | CTACAATATCATTCA[C/T]GAAAATAACAAAAAG | 11124 |
rs112580559 | in-del | -/AG | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50891321 | ATCTTCCTTTAGCCC[-/AG]AGAAGTTTGGTCTTC | 11124 |
rs112586674 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50633634 | CCAGCAGGGAATAAG[A/T]ATCTGTGGGTCTATG | 11124 |
rs112594267 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50778848 | ACACAGACACACACA[C/G]ACACACACACACAAA | 11124 |
rs112597061 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50715827 | TTTTTTAAAAAGGGG[A/G]AAATTAGGTATAGCA | 11124 |
rs112602593 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465977 | ATCGAGAAAGGCCTT[G/T]CACTCTGAACTGATG | 11124 |
rs112615362 | snp | A/G | 0.5 | 0 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50801642 | ATACCTTTGTAGAAT[A/G]CCATTTTCCTGTGGT | 11124 |
rs112615512 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50838859 | TCAGATTCAAATTCA[A/C]CTCTGGCCAATCCAT | 11124 |
rs112615680 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50859108 | CTCAAGAAAGTAGGC[A/C]TCAAAGGAATATATC | 11124 |
rs112616027 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50857663 | GAGCATCTCCACCAA[A/C]AAATTACGTGGGAAG | 11124 |
rs112616951 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50588336 | ATTTGTCAGGCAATT[C/T]GTGTATCTCTAATTC | 11124 |
rs112618522 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50735600 | GTTAAGAAGTTTTTT[G/T]GTTTTCTTGTTTTTT | 11124 |
rs112620393 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50900535 | CCAGTCTGACTCCAA[A/G]TTCACACACTTTGAA | 11124 |
rs112632642 | snp | A/G | 0.170408 | 0.236992 | intron-variant | FAF1 | GRCh38.p7 | 1:50649962 | ACAGAGTAAGACTCC[A/G]TCAAAGAGAGAGAGA | 11124 |
rs112652732 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50534439 | AAGCACATGCCACCA[C/T]ACCCAGCTCATTTTT | 11124 |
rs112654194 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50813646 | TAAAAATTTTTTTGT[A/G]GAGACGGAGTTTCAC | 11124 |
rs112662430 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50476395 | GGGATTTGGCCAAAT[C/G]TTAGTGGTTGATTTC | 11124 |
rs112664585 | snp | C/G | 1.69628e-05 | 0.00291224 | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959836 | CGAGTTCCGCGGCTC[C/G]GGGAGCGAAGCGCGC | 11124 |
rs112664721 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50499428 | ACATTTTACTCGATT[C/T]CTATTTTACTGGAAA | 11124 |
rs112666914 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50837233 | AGTGCTGGGATTACA[C/G]GCGTGAGCCACCGTG | 11124 |
rs112678420 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50644476 | CTGGTATTCAGCTAA[A/T]GACTTGGGGAACCCC | 11124 |
rs112695547 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50928649 | TCAGCCGAGCATGAT[G/T]GCGGGCGCCTGTAAT | 11124 |
rs112701504 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50910617 | AGCCTTGCTGTGGCC[C/T]TGCAGTTCGATCTCA | 11124 |
rs112702917 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462655 | ATCTGGGGCAAATTT[A/G]CATTGAACACGCTGA | 11124 |
rs112705281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50816012 | AGCCTAGGCGATAGA[A/G]TGAGATTCCGTCTTA | 11124 |
rs112708415 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50595519 | AATGAATCTACTCAA[C/T]TACACAGTCAATAGC | 11124 |
rs112717424 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50763127 | CTGGGGCATGGTGGC[A/G]TGCGTCTGTAGTCCC | 11124 |
rs112736640 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50802095 | TTATGATTACTATTC[-/T]TTTTTTTTTTTTGAG | 11124 |
rs112741026 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50458966 | TCCCCTGCCCTGCCC[-/T]TTTTTTTTTTCTTTT | 11124 |
rs112748369 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50763280 | AAATACATAAAATAT[A/C/G]AAATAAAACAAAATA | 11124 |
rs112753768 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50838558 | GAATTATAAATTAAA[A/T]ATATATATATTTTAT | 11124 |
rs112754181 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50882447 | AAAAATACAAAAATT[A/T]AAAAATTAGCCAGGC | 11124 |
rs112759976 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50867844 | GTACCTACCCAGAGG[A/G]AAAGAAGTCATTATA | 11124 |
rs112764482 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50713251 | AAATAATGAAACAGT[A/T]AAAAAAAAAAAAGGC | 11124 |
rs112773214 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50618303 | CTTTCCTCTTAACAC[C/T]GCTTTAGCTGCATCC | 11124 |
rs112779134 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50538728 | TTCATTATCCATTTA[A/C]CCTATGCAAATCAGT | 11124 |
rs112780433 | snp | C/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50935747 | AAAGTGCTGGGATTA[C/T]GGGCATGAGCTACTA | 11124 |
rs112793586 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50591529 | ATACAAAAATTTCAC[C/T]GGGCATGGTGGTGGG | 11124 |
rs112796721 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50503530 | AGCCTGAGGAGACTC[A/T]CTTGGGCCCAAGAGT | 11124 |
rs112808077 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50454575 | CATGTGGTCAATCCA[C/T]GTTTACCGGACTAAT | 11124 |
rs112809024 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50477319 | AGTATGGCATCTGAC[A/T]CATAATAGGCTTCAG | 11124 |
rs112809743 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50913813 | AGAAATAGAGCAGGA[A/G]GAACTTCCTAGACTT | 11124 |
rs112810143 | snp | G/T | 0.280785 | 0.248097 | intron-variant | FAF1 | GRCh38.p7 | 1:50664667 | GGCATGGTGGCGGGC[G/T]CCTGTAGTCCCAGCT | 11124 |
rs112820007 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50730336 | TATTACTTTAAAAAT[A/C]TCTTCTTAATCTGTA | 11124 |
rs112832934 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50716865 | GCGACCCACTCGGGT[C/T]CCCTTCCACGCTGTG | 11124 |
rs112833436 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50755178 | CAAGGCAAGTCCCTT[C/T]GACCTACGAGCCTGT | 11124 |
rs112833489 | in-del | -/T | 0.211212 | 0.246973 | intron-variant | FAF1 | GRCh38.p7 | 1:50935475 | CTGATTTACTCTCTC[-/T]TTTTTTTTTTTTTGA | 11124 |
rs112834625 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50728468 | GTCCCAGTAAGGAAC[C/T]TGGATTTTTATTAGA | 11124 |
rs112848454 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50831451 | TGCAGATACTGGTGT[-/C]CTACATCTGCCTTCC | 11124 |
rs112854770 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50452880 | TCCAAATTTCTCATC[A/T]GTAAGTTGGTGACAA | 11124 |
rs112879948 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865850 | TAATAATAATAAAAG[A/G]AAAAAAAAAAGAAAA | 11124 |
rs112888808 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527950 | ATCACAGCTCACTGC[A/T]GCCTTGACCTCTTGA | 11124 |
rs112893512 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50911204 | CAGCCTCCCAAGCAG[C/T]TGGGATTACAGGCCA | 11124 |
rs112898078 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | FAF1 | GRCh38.p7 | 1:50621087 | GGGGGCTCCTCCCCT[A/G]CTCAAGTGTTGGTCT | 11124 |
rs112902422 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50536233 | TCATTTTATTCCAAC[C/T]GAGTCCATAACAAAC | 11124 |
rs112903935 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50857698 | ACCATAACACACAGT[A/G]AAATAAGAGAAAAAC | 11124 |
rs112910381 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50500133 | CCAATCAAAATACCA[C/T]CAAAAATTTTTTTGG | 11124 |
rs112914273 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50748150 | ATTAAACTTGAAGTA[C/T]AGTTGGTCTGCAAAG | 11124 |
rs112915276 | in-del | -/T/TT | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50837747 | GAAAGGGGAAGCTCC[-/T/TT]TTTTTTTTTTTTTTG | 11124 |
rs112922656 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50710837 | TCAATTTCCTGACCT[C/T]GTGATCCGCCCATCT | 11124 |
rs112928681 | snp | C/T | 0.287867 | 0.247116 | intron-variant | FAF1 | GRCh38.p7 | 1:50456006 | CTTGAGCCTGGGAGG[C/T]GGAGATGGCAGTGAG | 11124 |
rs112931784 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50828460 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 11124 |
rs112940663 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | FAF1 | GRCh38.p7 | 1:50519059 | TTTCACGGCCAGGCA[C/T]GGTGGCTCACGCCTG | 11124 |
rs112981140 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672581 | AGCCACGGCGCCTGG[C/G]CAGCAATTTAAGTTT | 11124 |
rs112981353 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50474407 | TTTCAGGGGTAGTTT[G/T]TTTTTTTTTTAAATT | 11124 |
rs112982684 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50681782 | CCCTGGCCTCCCAAA[A/G]TGCTGGCATTACAAG | 11124 |
rs112995235 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50614519 | TTTGATCAACACATA[A/G]TAATATTAGAAATCT | 11124 |
rs112995534 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50551535 | CCCACAAAACTTTAA[A/G]AAGTCACTTAGAAAG | 11124 |
rs113001878 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | FAF1 | GRCh38.p7 | 1:50501989 | GGTGAACATTCAAAA[A/C]ATTGTGAAAAATATA | 11124 |
rs113007720 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50928238 | CAAAAATATTGGTTC[A/T]ATTTCAAAAGTGGCC | 11124 |
rs113011203 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50708373 | AAACATAACCCCAAG[A/G]TTTCTGGCCTAAGTA | 11124 |
rs113011226 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50714347 | TCTCTACTAAAAATT[-/T]AAAAAAAAAAAAAAA | 11124 |
rs113015905 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50504976 | GTGACTCCTATCATA[C/T]GCAGATTAAATTTTG | 11124 |
rs113017811 | snp | A/T | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50827635 | ATCAATAAATACTAA[A/T]AAATAAATAAATAAA | 11124 |
rs113026235 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50736489 | GCACAGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 11124 |
rs113028610 | snp | C/T | 0.145642 | 0.227177 | intron-variant | FAF1 | GRCh38.p7 | 1:50498774 | AGAATTGCTTGAACT[C/T]GGGAGGCGGAGGTTG | 11124 |
rs113031651 | in-del | -/ACAA | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50592057 | ACAGAGGGGAGAAAG[-/ACAA]ACAAAGTTCTTGCCT | 11124 |
rs113040481 | snp | G/T | 0.031825 | 0.122064 | intron-variant | FAF1 | GRCh38.p7 | 1:50771295 | CACAGCAAAAGAAAC[G/T]ATCAACAGAGTAATC | 11124 |
rs113042024 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50660637 | TAGCTGGGATTACAG[A/G]AGTGTGCCACCACAC | 11124 |
rs113052493 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50456205 | TCAAGTTATCCTCCT[C/G]CCTCAGCCTCCTGAG | 11124 |
rs113053576 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50663694 | TGGCGTGAGCCACCG[C/T]GCCCGGCCAGAAGCA | 11124 |
rs113069567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50619518 | GCTGGGATATGAAAT[C/T]CTTGGTTGAAATTTA | 11124 |
rs113075317 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50922320 | AAAAATTAGCTGAGC[A/G]TGGTGGCAGGCACCT | 11124 |
rs113080090 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50771980 | CAAAAAAAATTGACA[A/G]AAGTAGAGCCCTTGG | 11124 |
rs113084288 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50821874 | CACTATAAAGAAGTA[C/G]ATTGCAGACAACTTA | 11124 |
rs113086742 | in-del | -/TTCAAT | 0.217851 | 0.247924 | intron-variant | FAF1 | GRCh38.p7 | 1:50789740 | TCTCTTTCTCAACCC[-/TTCAAT]TACTCTCCTTTACTC | 11124 |
rs113096152 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50565517 | TCTAATAAGCAGCTT[C/T]TGTCGCTTTGGTCAC | 11124 |
rs113096493 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50623315 | GCTCACACCTGTAAT[C/T]CTAGCACTTTGGGAG | 11124 |
rs113104776 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687274 | GTTTCCTTTTTATAT[C/T]TCAATGTACAACTCA | 11124 |
rs113113684 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50725606 | GATTACAGGTGTGTG[C/T]CACCATGCCCAGCTA | 11124 |
rs113119450 | snp | C/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50770144 | AACCCACAGCCAACA[C/T]CATACTGAATTGAGC | 11124 |
rs113123268 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50957052 | AGATAATATAAAAAA[C/T]AGGAAGAATCATCAC | 11124 |
rs113145700 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50885041 | ACTTCCTTTAGATTT[C/G]TCAATTTATTGGCAT | 11124 |
rs113146201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50519315 | GCCTGGGTGACAGAG[C/T]GAGACTGTCTCGAAA | 11124 |
rs113157291 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50721513 | CCACCGTGCCCGGCC[A/G]GAAAAAAAAATTACA | 11124 |
rs113177430 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50724029 | GCTGGGATTATAGGC[A/G]TGAGCCACCACACCC | 11124 |
rs113179718 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50880171 | CCAGTAGTGTCTAAG[A/G]AGCATGCTTTCATGA | 11124 |
rs113191566 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50625059 | GGCGTGCACCACCAC[A/G]CCCAGCTAATTTTGT | 11124 |
rs113199665 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50457625 | AGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11124 |
rs113206168 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50896309 | AGTATATGGATTGTT[C/T]GTAACACAAAGGATA | 11124 |
rs113214638 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50873133 | AGGTGATAATTAGCA[-/T]TTTTTTTTAACAATA | 11124 |
rs113232576 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | FAF1 | GRCh38.p7 | 1:50642931 | CTGCAACCTCTGCCT[A/C]CCAGGTTCAAGCGAT | 11124 |
rs113240717 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50514065 | ACTTGCTGAATGAAT[A/T]GTATGGGAAAAACAA | 11124 |
rs113252621 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50719363 | GTAACAATCTTAAAA[A/C/T]CATGTTTAACGAAGG | 11124 |
rs113253522 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50522654 | GTACCCCGTAAGTAC[A/T]GAGCCCAAGAATCAA | 11124 |
rs113283551 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50891599 | CCCTCAGCTGCAGGT[A/C]TGTTGGTGTTTGCTG | 11124 |
rs113307988 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50729350 | GTGAGCCACCACGCC[A/C]GGCCTATCTACTCAT | 11124 |
rs113312279 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50925475 | CCAAAAAAAAAAAAA[-/A]TCCCACTACTACAAA | 11124 |
rs113315055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468844 | CAAGTGATCTGTCTG[C/T]CTCAGACTTCCAAAG | 11124 |
rs113317642 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50896455 | AAAAATGAGAAAAGA[C/T]GTAAAAGGAATATCC | 11124 |
rs113319965 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50756623 | TTAGTCCATTTTCAC[A/G]CTGCTGATAAAGACA | 11124 |
rs113342815 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50653104 | TCATGTATGAACATT[A/C]TTCTTTTATTTTTGT | 11124 |
rs113348171 | snp | C/G | 0.2776 | 0.248472 | intron-variant | FAF1 | GRCh38.p7 | 1:50660608 | AAGCGATTCTCCTGC[C/G]TCAGCCTCCTGAGTA | 11124 |
rs113351536 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50816666 | TAGCTTCTTTTGCTC[A/G]GCAGAAGCTCTTTAG | 11124 |
rs113353244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50839803 | GCCATCCCAAGATAC[C/T]TGAACAAGAATAAAA | 11124 |
rs113363749 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50584995 | CTAAACTTTCTGTGA[C/T]ACCTGTAGACCGAAG | 11124 |
rs113369846 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50892470 | TAGAGCTGTTCCTAT[A/T]TGGCCATCTTGGAAC | 11124 |
rs113371078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50778026 | ACAGCAGCTTGGTAA[C/T]GCTAGAAAGAACCCA | 11124 |
rs113389179 | snp | A/G | 0.110872 | 0.20771 | intron-variant | FAF1 | GRCh38.p7 | 1:50672234 | GTATTTTTAGTAGAG[A/G]CGGGGTTTATCTTGG | 11124 |
rs113391958 | snp | A/C/T | 0.00676944 | 0.0578265 | intron-variant | FAF1 | GRCh38.p7 | 1:50614818 | CACTCCAGCCTGGGC[A/C/T]GCAACAGCGAAACTC | 11124 |
rs113402151 | snp | C/T | 0.23846 | 0.249734 | intron-variant | FAF1 | GRCh38.p7 | 1:50655000 | TTTGAGATGGAGTTT[C/T]GCTTTTGTCGCCCAG | 11124 |
rs113405338 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50885135 | GTTTTTCATCTCTGA[C/T]TTTATTTATTTGGGT | 11124 |
rs113412687 | snp | G/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50925255 | TAAGACTCAAAACTA[G/T]AAAACTGCTGGGTGG | 11124 |
rs113416810 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50857795 | TATTAAAGATATGGC[A/G]TTTAGACTTTATTAA | 11124 |
rs113417399 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50477435 | TCATTTTTTATATGG[A/G]GAAATTGATGCCCAG | 11124 |
rs113433941 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50847211 | ATAAAAATTGAAGAC[C/T]AATGTATTAATTATA | 11124 |
rs113454428 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50738228 | GTGGGCAGATCACCT[A/C]AGGTCAGGAGTTCAA | 11124 |
rs113466952 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | FAF1 | GRCh38.p7 | 1:50906595 | GAAGAGGTCCTTCAC[A/G]TCCCTTGTAAGTTGG | 11124 |
rs113471094 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50936242 | CTCACAAATTAGTAA[G/T]AAAGACAAACAGATA | 11124 |
rs113472894 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50874882 | TCAAGCAGTTCTCCT[C/G]TCTCAGCCTGTAATG | 11124 |
rs113502165 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | FAF1 | GRCh38.p7 | 1:50496745 | TACAAAAAAATCAGC[C/T]GGGCATGGTGGCACA | 11124 |
rs113502667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50585232 | TTCTAAACTTTCCAC[C/T]TCCTTACTGCAGTGG | 11124 |
rs113503385 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50828214 | GGAATACTTGATTTA[C/T]GACAAAGATGGCACT | 11124 |
rs113512950 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50527391 | ATTCCAGATACAAGT[C/T]CCTTATTATTAGATT | 11124 |
rs113513207 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | FAF1 | GRCh38.p7 | 1:50567779 | ATGTATTCTCATATT[A/T]AGCCCTTATTTATCA | 11124 |
rs113525142 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50692795 | ATTTCTTTGGATTTT[C/T]TATTTGCATTTCCCT | 11124 |
rs113536179 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50885314 | CTCTCTCTCTCTCTC[A/T]CACACACACACTCTC | 11124 |
rs113541449 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50688386 | TCAAAGATGTATTTG[C/T]ACACCCATGTTTATA | 11124 |
rs113550922 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50458656 | ACGCATACAATGATG[C/G]GTTTTCTCATAAAAT | 11124 |
rs113553568 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | FAF1 | GRCh38.p7 | 1:50881736 | ATCTCTCCCATTACA[G/T]GAGTGGTTTCTAAAA | 11124 |
rs113554476 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50453268 | ATGTGCTCCTCAGGC[C/T]CAGTGGGCTAGGGAG | 11124 |
rs113562818 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50941552 | TTTGTAGAGACAAGA[A/T]CTCACTATACTGCCC | 11124 |
rs113565035 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50514576 | ATAGTTTGTGTAGGA[C/G]TATAAAAACAGAGAT | 11124 |
rs113565430 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50786081 | AGGCTACAGTGAGCC[A/G]CGATCACGCCACTGC | 11124 |
rs113568523 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50488225 | CTGTCCTCTCCCCCA[A/C]TGTACCCCAACCTCT | 11124 |
rs113574655 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50709549 | CAAAATTATACTTCT[C/G]AAAGGTTAATTGCCC | 11124 |
rs113581235 | snp | A/T | 0.0788843 | 0.182262 | intron-variant | FAF1 | GRCh38.p7 | 1:50673013 | CTATAATCCCAGCAC[A/T]TTGGGAGGCTGAAGC | 11124 |
rs113581784 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50582915 | CTGGAATTTTAAGTA[C/T]ACTTAGCAAATGAAT | 11124 |
rs113582845 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50833902 | TGATCACATTCCAGG[C/T]GCTCATGAAACCACA | 11124 |
rs113587257 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50889771 | ACATTTGCTGAGGAG[A/T]GCTTTACTTCCAACT | 11124 |
rs113597763 | snp | C/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50928237 | GCAAAAATATTGGTT[C/G]TATTTCAAAAGTGGC | 11124 |
rs113598997 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50599271 | GTGTGTGCCACCATG[C/T]CTGGCTAATTTTTGT | 11124 |
rs113602989 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50480583 | TTCTGCCTAAATGGA[G/T]CCTACATTCTAGTAG | 11124 |
rs113609040 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50821809 | TTGATACCCTTTTTT[A/G]AAATCACAAATGGTT | 11124 |
rs113611257 | snp | A/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50755431 | GCCTTGGGCAGCTCC[A/G]CCCTTGTGGCTTTGC | 11124 |
rs113611542 | snp | C/T | 0.111928 | 0.208413 | intron-variant | FAF1 | GRCh38.p7 | 1:50663531 | CCTCAGCCTCCCAAC[C/T]ACCTGGGACCACAGG | 11124 |
rs113618923 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466276 | AAGGATAACAGTAAG[G/T]TTTCTTGCCTGAACA | 11124 |
rs113620896 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50451215 | AAAGAAAAATTAAAG[A/G]AAGAACAAGGGGAGA | 11124 |
rs113623907 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50943517 | ACTCTTGTCAGTGAA[C/T]TGAGGCAGACCTTAA | 11124 |
rs113631365 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50650493 | GGCATGGTGGTATAC[A/G]CCTGTAATCCCAGCT | 11124 |
rs113631860 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922180 | TCAAAAAAAAAAGGC[A/C]AGGCGCAGTGGCTCA | 11124 |
rs113632692 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50672031 | TTCTTTTTTTTTTTT[-/A]TTATTATTTATTTAC | 11124 |
rs113652958 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440828 | CCTGGAGACCCAAGG[C/T]AGCAGCAGTAAATAA | 11124 |
rs113664530 | in-del | -/A | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50596046 | ATTGCTCTGGCAGAT[-/A]AAAAAAAAAGGGAAG | 11124 |
rs113666066 | in-del | -/TT | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50493035 | AAAGGATTAAACTTC[-/TT]TTTTTTTTTTTTTTT | 11124 |
rs113686078 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50870381 | AAAATCACTTGAACG[C/T]GCGAGGCACAAGTTG | 11124 |
rs113724622 | in-del | -/ACTA | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50790061 | GTCTAATTCCACACT[-/ACTA]ACTAACTATAAAGTT | 11124 |
rs113730976 | snp | C/T | 0.211819 | 0.247067 | intron-variant | FAF1 | GRCh38.p7 | 1:50751413 | GATCTCGGCTTACTG[C/T]AACCTCTGCCTCCTC | 11124 |
rs113738137 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50882527 | GAATGGCTTGAGCCC[A/G]AGAGGCAGAGGTTGT | 11124 |
rs113758665 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50562425 | TTCAACCACTGACCC[-/T]TTGTTCCCCATACGT | 11124 |
rs113771907 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50456739 | GGAGTATACAGTCTA[A/G]GGCAGAATGCTGACA | 11124 |
rs113796433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50733341 | CCATCTGTCTCCAAT[C/T]TTCTATTATTACACC | 11124 |
rs113808476 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50715337 | CCAGGCACAGTGCTG[C/T]GTGCCTGTAATCCCA | 11124 |
rs113809118 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50474845 | ATACAGAGCCTCTTG[C/G]TTCCCTACAAGGAAA | 11124 |
rs113814626 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50691458 | TGTTGCCCAGGCTGG[C/T]CTCAAACTCCTGACC | 11124 |
rs113815363 | snp | A/G | 0.311614 | 0.242289 | intron-variant | FAF1 | GRCh38.p7 | 1:50577253 | CCCTAGGCTGGGCGC[A/G]GTAGCTCATGCCTGT | 11124 |
rs113818968 | in-del | -/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50742204 | TAGTCCTAGCTACTT[-/T]AGAAGGCTGAGGTAG | 11124 |
rs113834846 | snp | C/G | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50512006 | ACCAGTGATGACGAG[C/G]TTTTTTTCATGTTTG | 11124 |
rs113836734 | snp | A/G | 0.21845 | 0.248001 | intron-variant | FAF1 | GRCh38.p7 | 1:50954169 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 11124 |
rs113840067 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50445288 | TTTTTATGCCTTTGC[A/G]TTGAGGTAAGGACAA | 11124 |
rs113845971 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50742267 | AGCAATGAGCCATGA[C/T]TGTACCGCTGCACTC | 11124 |
rs113849657 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50624019 | AGAAGAAAGAAGAAG[A/G]AGAAAGAAGAAAGAA | 11124 |
rs113858959 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50773385 | TGCACTTCCCTGTTC[A/G]TTGCAGGATTATTCA | 11124 |
rs113867571 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50854983 | TGTTTGAAAGGAAAT[A/G]CTCGATGGAACATTT | 11124 |
rs113870552 | snp | C/T | 0.144969 | 0.226867 | intron-variant | FAF1 | GRCh38.p7 | 1:50457782 | GGTGGTGTGCACTTA[C/T]AGTCCCAGCTACTGG | 11124 |
rs113883102 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50578638 | TTCTGGACTTTCTCA[C/T]CTCTAAAATGGGAAT | 11124 |
rs113884055 | snp | A/G | 0.120326 | 0.21374 | intron-variant | FAF1 | GRCh38.p7 | 1:50712407 | ACACCTGTAATCCTA[A/G]CACTTTGGGAGGCAG | 11124 |
rs113884278 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50489055 | TCATCTGTACATTGT[C/T]TGATTATCTCAGCTG | 11124 |
rs113885663 | snp | C/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50705742 | AGGGTCAACATTAGC[C/T]ATAATGAGCTACCTT | 11124 |
rs113889795 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50479277 | TTCCTCTCTGGATCA[C/T]GCCAGCTGCCTAGTC | 11124 |
rs113893923 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | FAF1 | GRCh38.p7 | 1:50831911 | TGAGCTCCGCCTCTC[A/G]TCAGATGAGCAGGAG | 11124 |
rs113899460 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | FAF1 | GRCh38.p7 | 1:50751393 | ATGCTGGAGTGCAGC[A/G]GCATGATCTCGGCTT | 11124 |
rs113900532 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50666312 | GGATCTCCTGGGCTG[A/T]TAAGATCCTCCCAAC | 11124 |
rs113910111 | snp | C/T | 0.151668 | 0.229849 | intron-variant | FAF1 | GRCh38.p7 | 1:50863101 | ATTCTCCAAGATAGG[C/T]CATATGGTAGGCCAC | 11124 |
rs113914786 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50647933 | GTTGGAGAAGGCAGC[A/G]CGGGAAGAAGGGCAT | 11124 |
rs113923006 | snp | C/G | 0.131723 | 0.220251 | intron-variant | FAF1 | GRCh38.p7 | 1:50690604 | AGACTGTCTCAAAAA[C/G]AAACAAACAAACAAA | 11124 |
rs113927178 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50887239 | GTTGTTGTTTTCTTG[C/T]AAATTTGTTTGAGTT | 11124 |
rs113928129 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50798783 | GCCTTTAATAGCTTA[C/T]GACTAAAATAATAAC | 11124 |
rs113928378 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50922780 | GCCAAGATCACGCCA[C/T]TGCACTCCAGCCCAG | 11124 |
rs113930101 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830569 | CATTTCCAAGTTTTA[C/G]CAACCTATATTTTGT | 11124 |
rs113934707 | snp | A/G | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50553827 | GCAAAACCAGAACCA[A/G]AAAGGATAAAGTTGA | 11124 |
rs113935355 | snp | A/C | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50947461 | AAGCCAGGTGTAATT[A/C]TTCTGTTAATTTTAC | 11124 |
rs113942530 | snp | A/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50900970 | AGAGGTAAAATCACT[A/T]CCCCAGGTACTGTTA | 11124 |
rs113943380 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50632026 | ATAGTATATACAGAG[A/G]TTGGTATTATCAGTA | 11124 |
rs113943392 | in-del | -/AT | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50739411 | TGTATGTGTATACAT[-/AT]GTGAGTGTATGTGTA | 11124 |
rs113948240 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50933752 | ATCCAAAACAGGGAA[A/C]AAAGAGAGGTTTAAT | 11124 |
rs113958834 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461357 | GTCGTATCTGCCCTG[A/C]CACACTTGGTTGGCC | 11124 |
rs113966662 | snp | G/T | 0.0829062 | 0.185956 | intron-variant | FAF1 | GRCh38.p7 | 1:50714277 | GGAGGCTGAGGCGGG[G/T]GGATTACTTGAGGTC | 11124 |
rs113972997 | snp | C/G/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50454229 | TCCTCTCATAGACCC[C/G/T]ATGTGCCAGACAATT | 11124 |
rs113979341 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50803412 | AATTTTGTAACCTTA[A/G]TATATTCACTGAACT | 11124 |
rs114000679 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50649766 | GCCAACTTATGAAAC[A/C]GCGTCTCTACTAAAA | 11124 |
rs114004988 | snp | C/T | 0.030278 | 0.119257 | intron-variant | FAF1 | GRCh38.p7 | 1:50618558 | ATGAGCCACCGCGCC[C/T]GGCCACCTAAATCTT | 11124 |
rs114005606 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50660018 | AAACTTCATACTTCC[C/T]CAATGTCTGTGGGAA | 11124 |
rs114010342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50815511 | GCTATGGTGAATACT[A/G]CTGTGATGAACACAT | 11124 |
rs114029798 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50919320 | GGAACTGCTAATCTA[C/T]ACAAAGAGCATCAGA | 11124 |
rs114040389 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50829815 | TTCCAGTTGTTTAAA[C/T]GTCATGAGCCAAACT | 11124 |
rs114042453 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674671 | TTATGACAGTAATAA[A/G]TAAATTTGAGGTTGT | 11124 |
rs114044884 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50579784 | TGGGGAGAGATGGTG[A/C]TTGCTTAAAAGGTAT | 11124 |
rs114047537 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50684189 | TTAACAAGGTGATAA[C/T]AGACAGAAATGCCAT | 11124 |
rs114051633 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50456712 | GTAAACAAGACACTA[G/T]TTCTGCTCTCAGGAG | 11124 |
rs114054699 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50555766 | CCCACTACTGAGTAC[C/G]CAAAGGAAAAAAAGT | 11124 |
rs114054879 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50809981 | AATCAATTGGCTTGG[C/T]GCAGTGGCTCATGCC | 11124 |
rs114066875 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50739438 | TGTGTATGTGTGTAT[A/C]TATGTGTATACACAC | 11124 |
rs114069560 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50650779 | AAAATTATTTCTCCT[A/G]TCTAGAAACCAAGAG | 11124 |
rs114101649 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50603117 | AAAAAGTATCCAATC[A/G]AACAACTATTAAGGC | 11124 |
rs114103441 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50655352 | TGGAAGACTCAAAGC[A/G]TTTAATTGTGCTTAT | 11124 |
rs114118335 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50896266 | CTCCAGCCTGGATGA[G/T]AGAGTGAGACCCTGT | 11124 |
rs114127904 | snp | A/G | 0.089084 | 0.191327 | intron-variant | FAF1 | GRCh38.p7 | 1:50457936 | AAAAGGTTATCGACC[A/G]GGCGCGGTGGCTCAC | 11124 |
rs114189060 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FAF1 | GRCh38.p7 | 1:50536754 | CTGGAAATTGGCACA[C/T]GACAAAGGCTTTAAT | 11124 |
rs114191600 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50756489 | TTCCTGCATTTTTCT[A/G]TCTTCTTCATAGCCC | 11124 |
rs114199486 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50803225 | ACTAAGTAACAGTAA[A/T]TGGTTAAGAGAATGC | 11124 |
rs114218874 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50937186 | TTACTATTAATTGTG[A/C]ATTAATAATAATACA | 11124 |
rs114227402 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50581970 | CAAAACTTATCTTCT[A/G]AATTCTTGTTATGGG | 11124 |
rs114230187 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50563478 | CAAGACTACCAAGGG[C/T]TTCCTGTCACTGTTT | 11124 |
rs114236327 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50612095 | GAAAAATTTAAAAAC[C/G]ATCATACACAGGAAA | 11124 |
rs114240567 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50703598 | TAACTTAAAGGGAAA[A/C]AAAGGAAAAAGGAGA | 11124 |
rs114244145 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50746705 | CAGGGGAGAAATTCA[A/G]GCGGGCTGCAGAAGT | 11124 |
rs114248434 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50626649 | GGTTAGTCATATTAA[C/G]GGGTCCGGTCTTTAC | 11124 |
rs114251634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50846699 | CAACTGTTGAAAGCA[C/T]GATGGAGCACTTCTC | 11124 |
rs114255012 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50891745 | GAGAGGTACCCAGCC[A/G]TGTGAGGTGTCAGTC | 11124 |
rs114256755 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50555946 | TGTGTATATATACAT[A/G]GTGTATATATATGGT | 11124 |
rs114269807 | snp | C/G/T | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50926121 | ACTCGGGAGACTGAG[C/G/T]GGGGAGGATCGCTTA | 11124 |
rs114282766 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50823065 | AGGCTTGAGGCACCG[C/T]GCCCGGCCAAGGCTA | 11124 |
rs114292605 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50770744 | CTTCACACAATTAGA[A/G]AAGACTATTTTAAAA | 11124 |
rs114294201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50719457 | TAAATAAACATTTGG[C/T]TTCACATAATTTCTA | 11124 |
rs114309116 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50590704 | GGGTCATTCTTGGCC[A/G]GGCGCCGTGGCTCAC | 11124 |
rs114323011 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | FAF1 | GRCh38.p7 | 1:50935537 | GTGCAGTAGCAGGGT[A/G]TCAGCTCACTGCAAC | 11124 |
rs114329036 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50643456 | TAATGGGAACAGTTT[C/T]TATTGCTGTATCTTT | 11124 |
rs114329455 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50487247 | CAGATCTGATGTTAC[A/G]CACAAAGTAAAACTT | 11124 |
rs114338459 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50838883 | AATCCATCAGATGGT[A/G]TTCTTTATACACTAA | 11124 |
rs114355074 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | FAF1 | GRCh38.p7 | 1:50904234 | GTGTGGATGCACCCT[A/G]AAGACATTAATGAAA | 11124 |
rs114361935 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50583934 | AGAACCTTAAAATAT[G/T]CCAAGCTCATAAATT | 11124 |
rs114386426 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50577640 | ACTATATGGATTGTT[C/T]ATATTGTTTTATTTA | 11124 |
rs114397816 | snp | C/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50442728 | GGGTGGGGGATATGG[C/G]GAAGTGGAGGCCCTG | 11124 |
rs114419967 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | FAF1 | GRCh38.p7 | 1:50694049 | ACATATACATGACAT[A/G]TATGACATATATATG | 11124 |
rs114421797 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50517900 | AAACAAATGAAAGAA[C/T]AATAAAATTTTGTTA | 11124 |
rs114422091 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50877949 | AACATTTTCACCTAG[C/T]AGCTGCTGAAACAAC | 11124 |
rs114427641 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50579256 | ACTGTATTTTTAAGT[A/G]TAAGTTATCTGCATT | 11124 |
rs114439578 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50905044 | CAACACCAGCCCCCC[A/G]CCCCACAACAGGCCC | 11124 |
rs114451631 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50937671 | GTTTAAAGTACTACA[A/T]GAGTATACCCATTTT | 11124 |
rs114469200 | snp | C/T | 0.00214464 | 0.032676 | intron-variant | FAF1 | GRCh38.p7 | 1:50612361 | CATTTTATTATAAGT[C/T]TGATAAATAAAGAGG | 11124 |
rs114477070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50834840 | CAAAAGGCATGAAAA[C/T]AAATAGTTATAATGT | 11124 |
rs114490430 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50593168 | ATAATAAGATATTAC[C/T]GAGGTTGTGAATGTT | 11124 |
rs114496917 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50473705 | ATGACCTTGGAGCAG[C/T]AGGCAGGGCCAGTGA | 11124 |
rs114518631 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50793108 | ACAGTAGAAACCCCA[C/G]ACTTGGTAGCCTAAA | 11124 |
rs114525520 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FAF1 | GRCh38.p7 | 1:50648753 | CCAACATGGAGAAGC[C/T]CCAGCTCTACTAAAA | 11124 |
rs114540602 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | FAF1 | GRCh38.p7 | 1:50863135 | ATGAGTTCCAATCAA[A/T]TTAAGAAAATCAAAA | 11124 |
rs114541491 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | FAF1 | GRCh38.p7 | 1:50932204 | AACCAATCATGCCTT[C/T]CCAATAGTCCCCCAA | 11124 |
rs114553539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50885693 | TCAATGTTACCATGA[A/G]TAAGTAAAGATTTAC | 11124 |
rs114562560 | snp | C/G/T | 0.0287743 | 0.116735 | intron-variant | FAF1 | GRCh38.p7 | 1:50612923 | TGTGATTTAAAAGAA[C/G/T]TACAACTTTCATTGT | 11124 |
rs114573542 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50803522 | CCTACCTTTTTGTTT[A/C]TCAAAGGCCTGTCTG | 11124 |
rs114574192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50614441 | AATGTTTATGTGAGT[A/G]TAAAAAAACAAAAAC | 11124 |
rs114581994 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | FAF1 | GRCh38.p7 | 1:50874863 | CAGCCTCAACCTCCC[A/G]AGCTCAAGCAGTTCT | 11124 |
rs114591390 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50829636 | TTCCCAAAAGTCCAT[C/T]TCTCTTTCAGAGCTT | 11124 |
rs114593374 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50456714 | AAACAAGACACTATT[G/T]CTGCTCTCAGGAGTA | 11124 |
rs114614699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50903518 | TGTATCTTTAGTATA[C/T]GTATAAATTAAATCA | 11124 |
rs114623137 | snp | C/T | 0.118584 | 0.212673 | intron-variant | FAF1 | GRCh38.p7 | 1:50676222 | GTCCAGCTTGGACAA[C/T]CTGGTGAAACCCCGT | 11124 |
rs114637295 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50499098 | TGGACCTTAAGGACA[C/T]TGTGCTTCAAATGTG | 11124 |
rs114653608 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | FAF1 | GRCh38.p7 | 1:50602796 | TAGGAGCCACCTCAC[A/C]CAGCCTAAAGTATTG | 11124 |
rs114653677 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50564995 | AATTTTTTGACATTT[A/T]AAAAAAACTTTTATG | 11124 |
rs114656273 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50821503 | GTTAATGTCTAAAGG[C/T]ATAGAGCCTTCATAA | 11124 |
rs114656854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50724661 | GCTTTCCCACTCCCC[C/T]TTCCTCCATTCTAGA | 11124 |
rs114657020 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50533779 | ATCTTACCAATATCT[A/G]TGAACATAACATCTC | 11124 |
rs114669264 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50699104 | AATGAACATGGTGGC[A/G]GTAATATATGCCATC | 11124 |
rs114670138 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50865937 | AGCTCAATTACAAAT[G/T]AAAGGGGAGATACTA | 11124 |
rs114690923 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50679182 | GTAACTGCTATATGT[A/G]GCAACAAAATTACTG | 11124 |
rs114698948 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50480068 | GATTTGCTCAACAAA[G/T]ATAGTTTATTTGCAT | 11124 |
rs114702551 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50896276 | GATGATAGAGTGAGA[C/T]CCTGTCTAAAAAAAA | 11124 |
rs114718546 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50893864 | TTAGAAACCTACCTG[A/G]TATTCTATTGTACTG | 11124 |
rs114720739 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50756481 | TCCAAACTTTCCTGC[A/T]TTTTTCTGTCTTCTT | 11124 |
rs114725961 | snp | A/T | 0.111606 | 0.2082 | intron-variant | FAF1 | GRCh38.p7 | 1:50672031 | TTTCTTTTTTTTTTT[A/T]TTATTATTTATTTAC | 11124 |
rs114727588 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50546899 | CAGTGTTAAACATAT[C/T]TTTCTATTTTATATG | 11124 |
rs114744819 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50766193 | TGCAATAATATTACA[C/T]CATTTGGATTTTTCT | 11124 |
rs114745413 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50713639 | AACGTAGAACCTTTT[A/G]AAAAAAAACAAAGAC | 11124 |
rs114770015 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50474527 | ACCCAGTGGGTAGTT[C/T]ATCTTAGTGCAGAGT | 11124 |
rs114796791 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50527230 | TTTGATTTGCAGTCA[A/C]CTGGTGAGTAATAAT | 11124 |
rs114802191 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50633450 | AAACAAAATCCCAAG[A/G]GGAGCAGTCCACAGA | 11124 |
rs114810178 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50671282 | TGTTGGTACGAACCT[A/G]TAATCCCAGTTACTC | 11124 |
rs114827875 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50552066 | TTGAGTTGCCAAGGC[A/G]GGCGGATCACCTGAG | 11124 |
rs114854195 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50797425 | TTGATTGAATGCCAG[A/G]TGTAGTGGCTCATGC | 11124 |
rs114854380 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50533152 | GTTGTTGCCCTGGCT[A/G]GAATACAATGGCATG | 11124 |
rs114859334 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50597951 | TCAGAGTGTCCTGAG[G/T]TCAAATTCACTTCTA | 11124 |
rs114889462 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50736007 | TATAGGCATAAGCTA[C/T]GGTGCCCGGCCAACA | 11124 |
rs114893712 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50490308 | GAGGCTACAACGAGC[C/T]GAGATGGTGCTACAG | 11124 |
rs114907757 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50713259 | AAACAGTTAAAAAAA[A/G]AAAAGGCATGTTTTC | 11124 |
rs114912404 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50449297 | TTATGCACAGTCGTA[A/C]AACCAGAAATTGTCG | 11124 |
rs114915405 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460400 | AAAATGGTTCCCAAT[A/C]ATAGTGCTGAAGTGC | 11124 |
rs114925906 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50481870 | TGAAGAATAGCAAGG[C/T]AGCCAATGTGGCGGG | 11124 |
rs114928936 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50839811 | AAGATACTTGAACAA[A/C/G]AATAAAAGAAAAAGA | 11124 |
rs114937664 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50445388 | AAGGTCTCAGAGCTA[C/T]TAAGGGCAGAGCCAG | 11124 |
rs114941695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550640 | AGTATTTAAGGACCA[C/T]ATCACCTAAACTCCC | 11124 |
rs114950173 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50634924 | AAGGAAAATTTAGGA[C/T]AACAGATAGTAACTA | 11124 |
rs114950434 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50680229 | ACACTTAGTTTTATC[A/G]CTAAATATTACAACT | 11124 |
rs114956358 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50836679 | CATATACCATTTCTT[C/T]CACATTTGAAGGTAA | 11124 |
rs114958856 | snp | C/G/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50494652 | ACTGCTCTCATATTG[C/G/T]GCTGTGCTACACTCA | 11124 |
rs114974481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50598676 | CATACTGTGCTGGGC[A/G]CAATGGCTCATGTGC | 11124 |
rs114987353 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50665623 | GTTTACATATTTTCT[C/G]TGGCTGTTTTTGCAC | 11124 |
rs115005065 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50472590 | TCTTAACATGAAGTA[C/T]TGTTTTGGTTGGGGG | 11124 |
rs115013662 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50593140 | CCTAATAATAAGATA[C/T]TATTATTCAGTAATA | 11124 |
rs115014241 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50652431 | TCATCGACTTTGCCT[A/G]TCATTCTTGGAACTT | 11124 |
rs115021760 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50934428 | CTCATATTTGATCAT[A/G]TAACACTGTCTTGGC | 11124 |
rs115021828 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50795296 | TCTCTGAAAAAGACA[A/C]TTTTCTAAATAGGAA | 11124 |
rs115023655 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50698633 | TTCTTGAAATGTTTT[C/T]CTCCCCAAGGATATC | 11124 |
rs115026108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528772 | CTTTCACCTCCTCTA[C/T]CTCTTTTGGCTCTGC | 11124 |
rs115032801 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50448516 | ACACAGGGGTGAGAA[C/T]AAACTTATTTGCCTG | 11124 |
rs115057676 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50685404 | AGATAGAAGGAGGGT[A/G]AGGTAAACTACTGCT | 11124 |
rs115069774 | snp | A/G | 0.030278 | 0.119257 | intron-variant | FAF1 | GRCh38.p7 | 1:50442902 | CTCAGAGCAAAGCAC[A/G]CTGTATTTGTATCTC | 11124 |
rs115069968 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50700964 | TCAATATTTATAAAA[C/T]GATCCCTACTGATTT | 11124 |
rs115070052 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50895220 | TTCAAAGGATCATTA[C/G]AGGCTACCATGACCA | 11124 |
rs115071227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50472853 | ATGGCTGTTACAGAA[C/T]AGCCTTGCAAAAACA | 11124 |
rs115072809 | snp | C/T | 0.112631 | 0.208878 | intron-variant | FAF1 | GRCh38.p7 | 1:50558188 | ACAGGTGTGAGCCGC[C/T]GCATCCAGCCTAAAT | 11124 |
rs115075933 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50452959 | CTATCTCCTTCACAC[A/T]TCCACTAGTGAGAGT | 11124 |
rs115087589 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50510828 | AGAATAGAGATTACA[C/T]GTAGAGGAAAAAGAT | 11124 |
rs115091877 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50809088 | AGATCATCAAAGATA[C/T]AATATATCAGAAACT | 11124 |
rs115100714 | snp | A/G | 0.114738 | 0.210248 | intron-variant | FAF1 | GRCh38.p7 | 1:50713843 | CAGTGGCATGATCTC[A/G]GTTCACTGTAACCTC | 11124 |
rs115106551 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50537183 | GCATGGGAAATGGGT[A/T]CTATATGGAGTACAC | 11124 |
rs115108083 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | FAF1 | GRCh38.p7 | 1:50656577 | AAGGTTAAACTCTAC[G/T]TCAGCCAGTAATTAA | 11124 |
rs115108541 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | FAF1 | GRCh38.p7 | 1:50497654 | CCCCAGGTTTAAGCA[A/C]TTCTCTGCCTCAGTC | 11124 |
rs115110771 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50656984 | AGGAGGTCAAGGTAC[A/C]AGGATCACTTGAGCT | 11124 |
rs115111623 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50843796 | CTTTGATGAACACTT[A/G]GGTTGATTCCATATC | 11124 |
rs115113672 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50626038 | AAACCATACTTGTTG[C/T]CATGTTTTTGCATAT | 11124 |
rs115123066 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50540929 | AAGGCAACTTAAATC[A/G]TGTGTTTTCTTATGC | 11124 |
rs115131550 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50800551 | GCCACATTTACTCTG[C/G]ATGAAAATCTTTCTG | 11124 |
rs115136563 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50721176 | CTTTGGGAAATTTTT[A/T]TTTTTTCTTTTGAGA | 11124 |
rs115139154 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50514259 | GCCATATTTATCTCT[C/T]TATTCTGACCCCCAA | 11124 |
rs115152865 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50522009 | TAAACTGATCTATCA[C/G]CAGGCACTTTAAGAA | 11124 |
rs115154906 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466544 | AGACTGGATGAGAGC[A/G]CTTAGATAATGCCAG | 11124 |
rs115177415 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50867337 | AAGATAAATAGATGA[A/C]ACTTAACTAAACTCA | 11124 |
rs115180668 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50486339 | TAGCTCTAATAATTC[A/G]ACTGTGTTCTAAGTT | 11124 |
rs115185740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50946616 | CTGAGTTTTATCCTG[C/T]TAGCAAGCTAACAAC | 11124 |
rs115209828 | snp | C/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50484408 | ATGAGAACAACGGAA[C/G]ACTTCAAACTGAAAG | 11124 |
rs115227691 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50893517 | TTGTTATCTTCCCAC[A/G]CTTTCTCCCAAACAA | 11124 |
rs115230564 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50709085 | TCAAAGGTAGATCTA[C/T]TGTACAACTATTCTC | 11124 |
rs115233920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949580 | ATTTTAGGCTTTGCA[A/G]GACATGCAGTCAACT | 11124 |
rs115281737 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50576411 | TAATGAAATTACTAA[C/T]ATCAAAGCTCAGACT | 11124 |
rs115282104 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467341 | TCTTTTTGGGACGGG[A/G]TCTCACTCTGTTACC | 11124 |
rs115288858 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50480711 | CTCGTAAGATTATAA[C/T]GGAGCTGAAAAATTC | 11124 |
rs115289319 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50644305 | TGTATTCACTGAGGT[A/G]TCTCTACAATGTGTA | 11124 |
rs115290385 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50948852 | AACAATCAGATCTCA[C/T]GTGAACTAACTGAGC | 11124 |
rs115295033 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50704217 | AGGCTATCTGCTGAA[C/T]AGTCCTTTCTGCCCT | 11124 |
rs115297002 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50544553 | GTTCTTAAAAGAAAT[A/C]ATCATAAAAATATTT | 11124 |
rs115307512 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50567836 | AGAGATAGAAAAATA[C/T]TCAGTTCACATGCAT | 11124 |
rs115307849 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50684927 | AGGCTATAAGATGGC[C/T]TAAACCAATTATACA | 11124 |
rs115310990 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50768988 | AAAATATACAAAAGA[C/T]TGAGTCCAGGAATTA | 11124 |
rs115314210 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465528 | CTAGGTGCCAGGAAT[G/T]TATTAGTTAACAAAT | 11124 |
rs115328949 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50764499 | GGAATCTCCTAGCTC[G/T]TTAACTCTGCAGGAC | 11124 |
rs115332164 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | FAF1 | GRCh38.p7 | 1:50681835 | CTTTTGTTTTTTTTG[G/T]TTTTTTTTCCTCTTT | 11124 |
rs115341174 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469750 | ACTTGGGCAGTGGTA[C/T]AGAGGGAAAGAGAAG | 11124 |
rs115343398 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50495724 | TAATTTACATTCCCA[A/G]TAACAGTGTACAAGG | 11124 |
rs115344987 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50822077 | AAAAGAATTCCAACC[A/G]GCAATCCTAGATCAG | 11124 |
rs115347886 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | FAF1 | GRCh38.p7 | 1:50486506 | TCTTTAACCATCAAA[A/G]TCTGTGAAGTCTTTT | 11124 |
rs115363550 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FAF1 | GRCh38.p7 | 1:50754364 | AGTACTCTCCACCAC[C/T]GAGGAAAGATCCTTC | 11124 |
rs115409586 | snp | A/G | 0.100944 | 0.200705 | intron-variant | FAF1 | GRCh38.p7 | 1:50588805 | ACAATGAAGGCCAGA[A/G]CCAGTGAAATGCACA | 11124 |
rs115427752 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50650583 | TGAGATCTCACCACC[G/T]CACTCCACCCTGGGT | 11124 |
rs115432382 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50599595 | ATTAAGTAATTTAAT[G/T]TATTTATTAAGTAAA | 11124 |
rs115436027 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50835041 | GCAGTTATGACAGAC[C/T]AAAGCTTTAATTCCA | 11124 |
rs115439921 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50819294 | GTGTGCCAAAATTCA[C/T]AGGGCTATCTACATT | 11124 |
rs115449133 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50900031 | CTTCATAAATACTTT[C/G]CATTTACTTTACTTT | 11124 |
rs115459241 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50946841 | AAGAGGAACTCACAG[C/G]CTAAAGAACCCAAAT | 11124 |
rs115461055 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50507155 | GGCACTTAGTAGGTA[A/T]TCAACAGATGTGCAC | 11124 |
rs115461924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824713 | ATGCCTATCAGTGGA[C/T]GAAGAGATTTAAAAA | 11124 |
rs115462138 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50824845 | GTGAAATAAGCCAGG[G/T]ACAAGGAGACAAATT | 11124 |
rs115470382 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50746735 | TTTACATAAGTAAAG[A/C]AAAGCCAAGTGCTGA | 11124 |
rs115471093 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50738072 | AAAATCATGTGATCA[G/T]TGTATAAATGTATTG | 11124 |
rs115478001 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50547331 | TAACCTAAAAAAGCA[C/T]ATCTCATCTGCCTGA | 11124 |
rs115485644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50930437 | AATGCAGTTTTACCA[C/T]TTAACTAGCCCTGTG | 11124 |
rs115517749 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50446887 | AGCCCCACTCTGTAG[A/G]TTAGGAAACAAGACC | 11124 |
rs115527919 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50480638 | ACACATAAGAAAAGA[C/T]AGTATGTGCCACATA | 11124 |
rs115532843 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50820118 | GCACAATGGTGGTTA[C/G]TAGGGGATGGGGTGG | 11124 |
rs115541002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739985 | AATACACATTAAGAA[A/G]TACATTGTATACCTT | 11124 |
rs115546817 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50529908 | GAAATTAATTTTCTG[G/T]GATTTGGGCCTCAGA | 11124 |
rs115553434 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50442640 | GACTGCAGCACCTGA[A/G]GCAGGCAATCTTATC | 11124 |
rs115561392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50472493 | AAGGCCTATGTCTGC[A/G]GCTATTTTGGTTGTC | 11124 |
rs115579144 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50885119 | TCAGACATAACGTGT[C/T]GTTTTTCATCTCTGA | 11124 |
rs115596210 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50482787 | TGATGCACTTATTTG[C/T]CTTCTGTATATTTTC | 11124 |
rs115596547 | snp | A/C | 0.0260105 | 0.111035 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461409 | TAATTATCATCACAC[A/C]CTTCAAAGTGTATAC | 11124 |
rs115623373 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50446579 | GCGACCTGAGGGCAG[A/G]AGCTGAGTAATACTA | 11124 |
rs115638846 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50508095 | AAAATAAGCACTGGT[A/G]AAGATATACAGAAAT | 11124 |
rs115639545 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50496354 | TCTCTCAATATAAAT[A/G]CTTAGAGATAGTAGG | 11124 |
rs115653780 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50497839 | AGGTGTGTGCCACCG[C/T]GCCCGGGCTCAAAAC | 11124 |
rs115658954 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50930180 | ATCATAATGCCAAAG[A/T]GGGAAATTCTCAATT | 11124 |
rs115660810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50640778 | TGGCACTGTTAATTC[A/G]TATCTAGTCTCTTTT | 11124 |
rs115661914 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50710894 | GGCATGAGCCACCGA[A/G]CCCGGCCAAGTGGCA | 11124 |
rs115671571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521327 | AGGCCCCATGGGAAA[C/T]AAAAATTCATGAGGA | 11124 |
rs115675951 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50692133 | AGATGGGAGGATCAA[G/T]GGAACCCGGGAGTTC | 11124 |
rs115680653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459636 | TGATTCTGTTGTCTT[C/T]TCTTCATCCCAAATT | 11124 |
rs115687062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50859309 | ATCTAAATAGGAAAA[C/G]AAGAAGTCAAACTAT | 11124 |
rs115688353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50933048 | AGTACTCCTGGGTCC[A/G]GCCCACAAAACCACT | 11124 |
rs115688798 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50529593 | TCACACTGAGAAACA[C/T]TGCCCCAGAAGAAAG | 11124 |
rs115691951 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50666202 | TACAGGCATAAGCAA[A/C]CGCGCCCGGCTGGAC | 11124 |
rs115693662 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50545602 | AAAAAAGAAAAAAGA[A/G]AAAAAAAACATTTTT | 11124 |
rs115694526 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50775996 | CAAATAAAACTGGAA[C/G]AGCTAGAAGAAGCAG | 11124 |
rs115703757 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50675523 | TTATAGAAAATGTAG[A/G]GTTCAGCATTACCAG | 11124 |
rs115719045 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50763817 | ATAACAGAACATTAA[A/C]ATTTCATTGAAGTGG | 11124 |
rs115735855 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50815441 | CATGGTGTATATGTA[A/C]CATATTTTCATTATC | 11124 |
rs115737264 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50516316 | CTGAACTTCCTTCCA[C/T]TCCACTTGTTCGTGG | 11124 |
rs115739112 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50893740 | TCAAAAATCAGCAGA[G/T]GGTGAAGCCAACCAA | 11124 |
rs115739604 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | FAF1 | GRCh38.p7 | 1:50694609 | TTATTAAGTATTTGC[G/T]ATGGTAACTACCATA | 11124 |
rs115745594 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50947211 | GGGAAAAAGAGGATG[A/G]GGAGGGCAAAAGAGA | 11124 |
rs115746354 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50734245 | AAGTTTTCTGAAAAT[A/T]ACAGTAATCATTTCT | 11124 |
rs115759222 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50897661 | TTTATAGAACAAGGA[C/T]AAAATGGACTGTGGT | 11124 |
rs115759686 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FAF1 | GRCh38.p7 | 1:50752545 | AAATAATTATCAGTT[C/T]TATTAATCTTTTTAA | 11124 |
rs115774053 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50661472 | GAATTAAGATACTAT[C/T]GCACATCATAGTACA | 11124 |
rs115776512 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50833408 | TAAGGTGTGTGGGGG[C/T]GGGTGTGTGGGAGAC | 11124 |
rs115797343 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50933741 | GATACAGACACATCC[A/G]AAACAGGGAACAAAG | 11124 |
rs115797810 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50787480 | GTTCCCCACTTAGGC[A/G]GATACAGCATCAACG | 11124 |
rs115851210 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50815031 | CCACTTCTGGGTATA[C/G]AATAAAAAGAATTAA | 11124 |
rs115854801 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50893188 | GGATTGGTCCCTGGT[A/G]CCTCATTTAACTCAT | 11124 |
rs115855502 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50937726 | TCCTTTATTGTTATT[A/C]TGCACTACAATTATT | 11124 |
rs115867430 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50579248 | TACGATATACTGTAT[A/T]TTTAAGTGTAAGTTA | 11124 |
rs115867929 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50518084 | GAAACAGTTTCATCA[C/T]ACAAAAAATATCCCT | 11124 |
rs115869376 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50486641 | GGTTTTTATAATGTA[C/T]GGTATCTTTTCCTGT | 11124 |
rs115886313 | snp | A/C | 0.030278 | 0.119257 | intron-variant | FAF1 | GRCh38.p7 | 1:50735785 | ACAGTGGCATGATCT[A/C]AGCTCACTGTAACCT | 11124 |
rs115895785 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50810763 | TAAGGTACAAAAATG[A/G]TCAGGCCAGGCACGG | 11124 |
rs115929764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50885922 | ATTATCTTAAGCGGA[C/T]AACAACTTGAAACTG | 11124 |
rs115953838 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50740419 | ATATGGAACTTATTC[C/T]TAACCCCTCCATGAG | 11124 |
rs115955738 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50721138 | TCATTCATGAAAATA[A/T]CAAAAAGTTGTTTCG | 11124 |
rs115973355 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50805211 | ATACTGTAATGTATT[C/T]TAAGAAGAACATCTT | 11124 |
rs115979111 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50944285 | ACCCAGCAGTCAGCT[A/C]AATTTAATGTGATAA | 11124 |
rs115996771 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50836468 | TTAGGGACAAAAATT[A/G]GACCAAAATAGTAAG | 11124 |
rs116014038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50450827 | TAATAATAATTATTA[C/T]AAACAACTATGACAA | 11124 |
rs116037786 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50573046 | CTATAAGTAGAAACA[A/G]ACAAACCACAGTAAA | 11124 |
rs116039828 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50615794 | TGAAAGTATTTTCTC[C/T]CATTCTGTATGTCAT | 11124 |
rs116052205 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50773998 | AAAGAATATTTCTAA[C/T]GCATAAATAAACTAT | 11124 |
rs116056817 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50826219 | GTGGAGAAAGCCACA[A/G]ATATTCTCAAAAGTC | 11124 |
rs116057146 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50703247 | AACTACAAAATAGTT[C/T]CACAATTATATTTTT | 11124 |
rs116060502 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50562683 | TCATATTATATATTA[A/G]CTCTTATGTCTGTTT | 11124 |
rs116065283 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50795555 | AACCTCAAAGCTTGG[A/G]GGTCCTCCTTAAAGT | 11124 |
rs116074529 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50572012 | AGTGTTAAAACTATA[A/G]TATAAAATAATTTCC | 11124 |
rs116081157 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50721462 | TCAGGATCCGCCTGC[A/G]TCGGCCTCCCAAAGT | 11124 |
rs116086296 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50915653 | TTAATCCACAAGGAA[A/C]CTCCCAGTTCCCAAA | 11124 |
rs116091456 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463368 | TGTATCCTTTTGCTG[C/T]AACAACTCATAACCA | 11124 |
rs116096835 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50497203 | GGAAACAATGACAGC[C/T]GACTTTTCATCAGAA | 11124 |
rs116102074 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50518805 | CAGTAGGTTGCTGTA[C/T]CATAAGTTAAATCTA | 11124 |
rs116115121 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50859047 | CATCTCAATAGATGC[A/G]GAAAAAGTTTTCAAT | 11124 |
rs116119980 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50582430 | AGCAGCACATAATAC[C/T]AAAATTGGACTTATA | 11124 |
rs116132367 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50932129 | AGATTTGGATGGGGA[C/T]ACAGCCAACCATATC | 11124 |
rs116138218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50832214 | TCCTCTACTCCAGTC[C/T]GCAGAAAAACTGTTG | 11124 |
rs116139765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50843671 | TATTTAACATAATGT[C/T]CTCCCGTTCTACCCA | 11124 |
rs116144893 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50592573 | AATATAACTACAATC[A/C]ATAAAGTCTAAAACT | 11124 |
rs116151857 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50572543 | GTATATGGATGTTCA[C/T]AGGTACCACATAGCA | 11124 |
rs116156264 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50679749 | TGAAAATATTGGTAA[A/C]TGCTATTTATTTCCA | 11124 |
rs116182873 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50619146 | TATGTGTGAGATGTG[C/T]CTCTTGAACACAACA | 11124 |
rs116192128 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50601573 | TGTACTCTCAGGCAC[C/T]CGGGAGGCTGAGGCA | 11124 |
rs116194089 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50794943 | TACCTGGCTAAATAT[A/T]TTTGTTTCTTAAGTG | 11124 |
rs116206962 | snp | A/G/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50619805 | TGTAGTGAGATTAGG[A/G/T]AAATTTTCATGGACT | 11124 |
rs116224281 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50515888 | CTGTATCACATACCC[A/G]AATTTTTATGTTCTT | 11124 |
rs116236548 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50583333 | ATTTTAAAGGATTTT[C/T]CATTTGACTGTCCTA | 11124 |
rs116247810 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50661198 | CACTAATATTTTCCC[C/T]TTATGAGATCTCATT | 11124 |
rs116273703 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50562482 | CCTTTAGTAAAGAAG[A/G]GCAAAATCTGCCACC | 11124 |
rs116274820 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | FAF1 | GRCh38.p7 | 1:50767671 | TTCAGCATTCTTAAG[A/G]AAAAGAAATTCTAAT | 11124 |
rs116276287 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50450718 | AAGTATCAGAGGGGG[A/G]ACTTAGGGGAATTGC | 11124 |
rs116293605 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50691132 | TAACCATGTTTAACA[A/T]GTTGAGGAACTATCA | 11124 |
rs116307259 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50720373 | CAATTAAATTTAAGT[G/T]GAACAGTAATCACAA | 11124 |
rs116315997 | snp | A/G | 0.0330485 | 0.124226 | intron-variant | FAF1 | GRCh38.p7 | 1:50590991 | TGTCTCCAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 11124 |
rs116371042 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50482099 | TGCATAAGTACCATC[A/C]CCAACAAAGAAGAGT | 11124 |
rs116372438 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471370 | ATACCCCAAATTTGA[A/G]AGGCTTTTCCCCCAG | 11124 |
rs116381848 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50552022 | ACTGCAGGCCAGGTG[C/T]GGTGGCTCATGCTCA | 11124 |
rs116400034 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | FAF1 | GRCh38.p7 | 1:50481249 | AGTGATTATAAAGTC[C/T]GCTGTAATGTAATGT | 11124 |
rs116402191 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50745091 | CCAGGAGTTCAAGAC[C/T]GGTCTGACCAACATG | 11124 |
rs116411807 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50650892 | TTTTCCTACTGGTAA[A/C]GCTTTAGATACCTAT | 11124 |
rs116412718 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50752459 | GTCCATGTAATGTAC[A/G]TAGGCGCTTCTTTCA | 11124 |
rs116414349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50787592 | ATGTGAGAAAATAAA[C/T]TTCTGTTCCTTATAA | 11124 |
rs116417963 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50939370 | ACTCTAAGCCTGGGC[A/G]TTACTGGTGTATAGA | 11124 |
rs116419094 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50537129 | CAAGTCTCTGGGTTT[C/T]TATGTTTTATTTAAA | 11124 |
rs116423083 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50610298 | TTCAAGCATTTTTCT[A/G]ATTGTGGAAGTATCC | 11124 |
rs116431759 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50873963 | ACCAGTCTTCAGCCC[C/G]TAGTATCTACATCCA | 11124 |
rs116442133 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50706098 | TCTTTCTCTACCAAG[G/T]TGTTTTTAAATTTCA | 11124 |
rs116452151 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50707686 | GCGATAGAGGGAGAC[A/G]CTGTCCCAAAAAAAA | 11124 |
rs116453297 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460691 | CAGGCTGGAGTGTAG[C/T]GGTGCGATCACAGCT | 11124 |
rs116483483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50635848 | TAAATAGAAATTTAG[A/G]TCAGCTACTAGGGGA | 11124 |
rs116496035 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462621 | ACAACCGTAGGGGTT[C/T]GGAGCAGACCATTAT | 11124 |
rs116502428 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50661539 | CATCTCATTCTTTTA[A/T]CATTCTTAGAAGAAA | 11124 |
rs116505675 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50730067 | TCCATGAAAATTTAT[A/G]AAAAATCCTCTGGAG | 11124 |
rs116513411 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50551733 | CAAAAGATCCTTTAG[A/G]TAAGATTCAGAAATA | 11124 |
rs116517024 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50679491 | GCCCAACAGATGATC[C/T]TGCCTCTCTACTCAG | 11124 |
rs116517491 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50561215 | AGGATGAACTCATCT[A/G]GGTTGGAATTCAAGC | 11124 |
rs116519860 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50758647 | TCTTCCATCTGTTAT[C/T]GTTTTCTTTCAGGCT | 11124 |
rs116526297 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50893168 | GTCACATATCTGTTT[C/T]TCCAGGATTGGTCCC | 11124 |
rs116534888 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50748707 | GTACTTATCTTTCAT[A/C]TATCTGCTTATGTTA | 11124 |
rs116536977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50782089 | AATCGTATATAGTAC[A/G]TAATACTTGATAATG | 11124 |
rs116539821 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50520345 | TTTGGAGAGGTAAAA[C/G]TGACATGTCAAAAAT | 11124 |
rs116545733 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50719651 | TCAAGTAGTACATGG[C/T]AAAACTGTCAAAACA | 11124 |
rs116546814 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50942842 | GCCATACATCATGGA[C/T]TGCGTTACGGGAGAG | 11124 |
rs116553473 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50551143 | CCTATTTTATATTGT[A/G]TGTACAGAGATTATG | 11124 |
rs116553800 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50659230 | GGGAAGATGAAGAAA[C/T]ATGAGGAAGAAAGAG | 11124 |
rs116571661 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50527195 | AATTGTAGCAGGTAT[A/G]AAGTGGTACCTCATG | 11124 |
rs116582233 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50522025 | CAGGCACTTTAAGAA[A/C]AACAAATGTAAACAG | 11124 |
rs116583643 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50514137 | GAGAAGAGCAAGATG[C/T]TAAGGAATGATATTT | 11124 |
rs116609105 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50616971 | CAGGCATGAGCTACC[A/G]CACTCAGGCTGTACA | 11124 |
rs116613651 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50957142 | ATGTGTTTAAGGTGT[A/G]TAGTTTTCCAAATAA | 11124 |
rs116620532 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50881645 | CAATCGGGAAGACCC[C/T]TGGCAACACCTGCAG | 11124 |
rs116622504 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50654511 | GAAATGACAGAGATA[A/G]GAAAGGCTTCAAACA | 11124 |
rs116626164 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50509555 | AAGTTGAGGCTGCAG[A/T]GAGCTGTGACTGTAC | 11124 |
rs116627611 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50703414 | TTGCACAAGTTGAAG[C/G]AGAAAAGTCACAGAA | 11124 |
rs116635037 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50456088 | TTAAACAAAAAAAAA[A/T]TTTTTTTTTTTAGAG | 11124 |
rs116644005 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50667686 | AGCTACTTGCCTAAA[C/T]GTCATTCACTTAGTT | 11124 |
rs116647844 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50931389 | GATAAAGACACACCC[A/C]AAACTGGAAACAAAA | 11124 |
rs116674217 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459971 | AATTCTGTCCTCAAT[C/T]AGTGGACGTATAGTA | 11124 |
rs116684960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50887206 | CCTGTTCACATCCTT[C/T]GCCCACTTGTTGATG | 11124 |
rs116691517 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50790900 | CAGTCTTTTAAAGAT[C/T]AGAATAGAAATTATC | 11124 |
rs116692933 | snp | C/T | 0.110519 | 0.207473 | intron-variant | FAF1 | GRCh38.p7 | 1:50670601 | AATTCTTCAAAATTA[C/T]ACTTTTATTATTTTT | 11124 |
rs116703300 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50628347 | TCATTGCTCTTTTTC[C/T]ACACACAGCTATCTG | 11124 |
rs116704217 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50782423 | TTAAAAGTTAAAAAA[C/T]AATAATTAAAAAATT | 11124 |
rs116725290 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50852994 | AACTTATCTTTTGTT[A/G]TAGCAAGCATCTGTG | 11124 |
rs116732144 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50935100 | TATTGAAAAATGTGG[C/T]AATAAGATCCATATA | 11124 |
rs116732283 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50668241 | GGCCAGTGTTTGCAT[G/T]TGGGGCCCTGGAGTC | 11124 |
rs116758989 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50917227 | TGCTGAGAACAAATT[A/G]AAAAGCTGAAAGATA | 11124 |
rs116763723 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50576408 | CTGTAATGAAATTAC[C/T]AATATCAAAGCTCAG | 11124 |
rs116765752 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50704116 | GCAATATGCCAATTA[G/T]CTGTAAATCAAACAA | 11124 |
rs116766155 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50835417 | CCTAAATTCAAATCC[C/T]CTAGTCACTGTCTAT | 11124 |
rs116779014 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FAF1 | GRCh38.p7 | 1:50794927 | CAGGCGTGAGCCACC[A/G]TACCTGGCTAAATAT | 11124 |
rs116788255 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50495731 | CATTCCCAATAACAG[C/T]GTACAAGGGTTCCCT | 11124 |
rs116790443 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50567528 | AGGAATTGTATTTTG[C/T]TTAAAGGAAATGGAT | 11124 |
rs116804106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916175 | GTCGTAGGAGGAAGG[C/G]TAGAATGCAGGACAG | 11124 |
rs116809636 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50645481 | GGTCTTTGTTTGCAA[C/T]TATATATCCCTGCTT | 11124 |
rs116827723 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50739057 | TTTTGTAGTTTTTTT[A/T]ATCTTTTGATAATTT | 11124 |
rs116843559 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50657364 | TCCTACTGTATCAAA[C/T]GAAGTTAGGATTGAA | 11124 |
rs116867071 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50935813 | GAAGTAATTATGAAC[A/G]CTACTAGTGATGTGG | 11124 |
rs116872937 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50688326 | CCATATGATTCAGCA[A/C]TCCCATTTCTTGGGT | 11124 |
rs116874533 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50881895 | TGCATTGAAAACATA[C/T]ACAGGTAAAGCATAA | 11124 |
rs116876459 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | FAF1 | GRCh38.p7 | 1:50778893 | TCGATTAACTTCCTT[C/T]CATGAAAAGTTTTGC | 11124 |
rs116922310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721813 | CTTTTTTGTAGAGAT[A/G]AGGTTCCACTATGTT | 11124 |
rs116927128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50516040 | ACATGTATCAACTGA[C/T]TTAATCTTCACAACA | 11124 |
rs116959423 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | FAF1 | GRCh38.p7 | 1:50818402 | AATTCCACTCTTAAG[A/C]ATTTACCCAAAAGAA | 11124 |
rs116982413 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50670581 | AGAAATACTGCAGTT[A/T]AATTAATTCTTCAAA | 11124 |
rs117003636 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50495056 | GCATGCAATGGGTAT[C/T]AATTACTTCATGGAA | 11124 |
rs117007449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471192 | GTATCCATGTGTTAT[C/T]GATGAAGTCAAGTCA | 11124 |
rs117056565 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50609505 | TTTTTCCACTTCAGC[A/C]TCCTGAGCAGCTGAT | 11124 |
rs117088556 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50535709 | TTAATGAGAAGGACT[C/T]TTAGCACTATATAGA | 11124 |
rs117088790 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50702381 | AGCCTGTTTAAATTT[A/G]AGGAAACTCACAATT | 11124 |
rs117125037 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | FAF1 | GRCh38.p7 | 1:50681296 | AAGTGATAAGCCTCC[C/T]TCAACCTCCCAAAAT | 11124 |
rs117193805 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50519111 | CCGAGGTGCGAGAAT[C/T]ACGAGGTCAGGTGTT | 11124 |
rs117209433 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FAF1 | GRCh38.p7 | 1:50868547 | AAGCATTTATAGCTG[C/T]AAATTTACCTCTAGG | 11124 |
rs117211656 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | FAF1 | GRCh38.p7 | 1:50844366 | CTTTGAAACAAACAT[A/G]GCTACAGGGAGAAAT | 11124 |
rs117221425 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50765365 | AATACATTATCTACA[A/G]AATTTAATACCTTTT | 11124 |
rs117250880 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50664751 | GAGAGTCGAGATCGC[A/G]CTACTGCACTCCAGA | 11124 |
rs117253261 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50646987 | AGTGTCTGGGATCAC[A/C]TGTGTGAGCCACCAC | 11124 |
rs117271353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50609062 | GTGCAAAATACCATT[A/G]TCCACTCACTTAACT | 11124 |
rs117288941 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50627481 | TGAAATATCCACACA[A/G]TGGAATATAATAAAG | 11124 |
rs117291672 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50745917 | GACAAGAAGATGAGG[A/G]AAAATTAGGAACTTC | 11124 |
rs117343996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50666243 | TGTTGAGACAGTGTC[C/T]TACTCTGTCACCCAG | 11124 |
rs117348566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50587033 | GCCTAGTACTCACCC[C/T]CTCCTTTGAGGCATC | 11124 |
rs117438533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50720598 | GGCACTTGGGGAACA[A/G]CTGACACAAACACAG | 11124 |
rs117467082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50625607 | GAGGGTAGGCGGAGT[A/G]TAAGCACCTTAGAAG | 11124 |
rs117470804 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50556041 | TCAGCTATAAAAAAG[A/C]ATAAGGTCTTCAATG | 11124 |
rs117479547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50638345 | CAGTATAACATTGAA[C/T]AGAACTTGCGCAAGT | 11124 |
rs117484059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50454960 | GATCTACTGAATGAC[C/T]AAATGGAAACTCCCC | 11124 |
rs117508236 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50607191 | ACATCTTTAGGCTTC[A/G]TGGTGCCCTTGTATG | 11124 |
rs117509722 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50597245 | TCTAGAAAACATGAC[G/T]TTAGCAGAAACACCT | 11124 |
rs117514254 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50631076 | ATTATAGGCATGAGC[C/T]ACAGTGCCCAGCCTC | 11124 |
rs117517023 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50727163 | ACCTTACAACCCACA[C/T]TAGTCATTCAATTAT | 11124 |
rs117528599 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50913743 | AAGACTAAAGATATC[A/G]TAAAGATACTAAAAA | 11124 |
rs117620032 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50866423 | TTGCCGATGATATAA[C/T]TGTATACCTAGGAAA | 11124 |
rs117707989 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50814881 | AAAACCAGAAGATAA[C/G]TGTTGGCAAGATGTG | 11124 |
rs117743346 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | FAF1 | GRCh38.p7 | 1:50880432 | CCAATGTGGCTGGCC[A/G]TATTCGGAGTAAGGA | 11124 |
rs117759475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521134 | CTATATTGAGCTAAG[C/T]AACACATGCATAACC | 11124 |
rs117776073 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50709429 | ACACTAGAAGGTGAT[G/T]CAATTCAACTGTATA | 11124 |
rs117776559 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50513941 | GCTTATTGTATTTCT[A/C]CATCTCTACATTTTC | 11124 |
rs117778880 | snp | G/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50495712 | TGGTGATTGTACTAA[G/T]TTACATTCCCAATAA | 11124 |
rs117824737 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50680823 | AATGGTCAGAATTTC[A/G]AGAGTTTTCATCTGT | 11124 |
rs117904132 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50746874 | ACCACCCTGCACAGA[C/T]GCAGGAAACTGCTCC | 11124 |
rs117905462 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50725241 | AAGAGCCTCTATTTT[C/T]TGGTAGGATCTGAGG | 11124 |
rs117928213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50944027 | GAAAGGACTGAATGA[C/T]GGCAGTCAGTCCAAT | 11124 |
rs117929904 | snp | A/G/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50917843 | TGGGAGAAAATGTTC[A/G/T]CAATACATTTATCTG | 11124 |
rs117943048 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50730096 | AGGGTGAAGGGGGTT[A/G]GAGCAGCATGCGGAA | 11124 |
rs117958180 | snp | A/C/T | 0.0165278 | 0.0893908 | intron-variant | FAF1 | GRCh38.p7 | 1:50710104 | CTAGGCTGAGGAGCT[A/C/T]GGAGTTCCAGAAGTC | 11124 |
rs117970346 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50793680 | TGCATTTTGCTTTCA[C/T]ACAGCAGGGTAGACT | 11124 |
rs117980316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610815 | CTTCAAATTAGCATT[A/G]TACCAAGGCACTAGC | 11124 |
rs118013600 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463150 | TGGCAGAGTATACCT[A/G]TGTGTTCAGCACCCA | 11124 |
rs118058004 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50925976 | ATCCCAGTGATTTGG[A/G]AGGCTGAGGCAGGAG | 11124 |
rs118072079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50868610 | ATGTATGTTCATTAT[A/C]ATTCAGTTCAAAGTT | 11124 |
rs118115679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50583055 | ATTCCAGAATTCCAA[C/T]AGAAGGAAAAAACTG | 11124 |
rs118176942 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50946449 | TAAAGTAGAGAACCA[C/T]TTAATTTGGGCAACA | 11124 |
rs137862727 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50648729 | GTAGGAAGTTCAAGA[C/T]CAGCCTGACCAACAT | 11124 |
rs137863218 | in-del | -/G/GG | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50476794 | AATTTAAAAGCTAGT[-/G/GG]GAAAAAAAACCAATA | 11124 |
rs137873747 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50531348 | AATGAATAAACAAAT[A/G]AAACAATAAATAGAT | 11124 |
rs137886504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50730833 | TTATATATATTGCTA[C/G]TTGCTACACGCTTTT | 11124 |
rs137886577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50780932 | GGGCCAGAATTGTGG[C/T]GGAAAAGGCTGAGCA | 11124 |
rs137888593 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50883093 | TAACCAGGAGGTCAC[C/T]GTTTGCCCCACCTGG | 11124 |
rs137890525 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50644888 | CTTGTAAGTTTCCAA[C/T]TGGGGCTGTCTTGCT | 11124 |
rs137930193 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50602605 | TCTCCCAGGTTCAAA[C/T]GATTCTCCTGCCTCA | 11124 |
rs137939242 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50515739 | ATAGCAGAACATAGA[C/T]ATACCTTCAAAAAAA | 11124 |
rs137942920 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50526549 | CTGCAAGCAATCCAC[A/G]TGCCTCTGCCTCCCA | 11124 |
rs137959438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902532 | TGTGGCTCACACTCT[A/G]TTTTGGACATGTACT | 11124 |
rs137963015 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50736021 | ACGGTGCCCGGCCAA[C/T]ATGTTATTTTATATC | 11124 |
rs137964098 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50949284 | TTATTCTGATGCAAA[C/T]TAAAGTTTGAGAACC | 11124 |
rs137971972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684965 | GTTGTATGAGGCACA[A/C]TATCACTGTGTGGTA | 11124 |
rs137974235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50769328 | ACCAGACAATGCCCA[A/G]GACCAGATGAGCTCA | 11124 |
rs137982755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869724 | CTACCTAGTATAGAG[C/T]TTTTTCTTTGAGGAT | 11124 |
rs137984542 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50568796 | CAGGGAAATCAACCA[C/T]ACTGTAGTCAAGGCT | 11124 |
rs137984861 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50810798 | TCACACCTGTAATCC[C/T]AGCACTCTGGGAGGC | 11124 |
rs137994124 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50537283 | TAAGTCACTGCTTAT[C/T]AGCTATGTTTTAGCC | 11124 |
rs138000558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50913406 | ATCAAGTGGCATGTG[C/T]AACTTACTCAGCTAC | 11124 |
rs138007267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824576 | TCCTCAAAAAACTAA[A/T]GACAGATTTACTGTA | 11124 |
rs138011693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620297 | GTCTGAATGAGTTGA[C/T]TTGAAGAACCAGTCT | 11124 |
rs138024184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50913839 | GACTTACTATGGCCT[A/G]AGTAAACCATCCCCC | 11124 |
rs138029094 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50945354 | AAGCTGGCTGAATAG[G/T]CAGGTCAAAGGTCCA | 11124 |
rs138043965 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50667146 | ATCTGAGAAAGATGG[C/T]AAGATAAAAAATTTC | 11124 |
rs138062016 | in-del | -/AAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931889 | ATAATAATAATAATA[-/AAT]ATAATAATAATAATA | 11124 |
rs138065801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50587119 | ATACTTCTTTCTATA[C/T]TTACCCCTTTTACTT | 11124 |
rs138065919 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50532902 | CTGCAGCCTTCAACT[C/T]GTGGGCTCAAGTGAT | 11124 |
rs138074417 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50688704 | GTAATCCCAGTTACT[C/T]GGGAGGCTGAGGCAG | 11124 |
rs138074659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653829 | GAGCCAAGATTGTGT[C/T]ATTGTACTCCAGACT | 11124 |
rs138079375 | in-del | -/AA | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50740317 | TTTGAGCAAAAACTT[-/AA]AAGGTGAAGGAAGCA | 11124 |
rs138082915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50608074 | GTGTGCTCAGAGTAG[C/T]AGCTCAAAGGCTGTT | 11124 |
rs138093581 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50486708 | AGTAAGCTCCTTGAG[A/G]GCTGGACTATGCCTC | 11124 |
rs138097320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50775843 | GTCAGAAAAAAATTC[C/T]ATCAAGTCTAAGTAT | 11124 |
rs138098116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50950552 | CAATAAATCCTTATT[C/T]ATAAAAACAGGCAGC | 11124 |
rs138100730 | in-del | -/TTTG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50605123 | AATATAAAAGGTTTT[-/TTTG]GTTTGTTTGTTTTTT | 11124 |
rs138103591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50878188 | CCCAAAATATAACAT[C/T]AAATTTAGAAATTTG | 11124 |
rs138108920 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50740141 | TCTTAGGGAGCTTAC[A/C]TTTGAGTAGGAATAA | 11124 |
rs138124566 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50588052 | AGCACTTTCAGAGGC[C/T]GAGGCAGGCGGATCA | 11124 |
rs138135161 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50704887 | TACAGAAACAGTTCA[C/T]ATATTTCTGAAAGAA | 11124 |
rs138144556 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50928609 | CAACATAGTGAAACC[C/T]CATCTCTACTAAAAA | 11124 |
rs138160522 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50917697 | AGGAAAGGAAAGGAA[A/G]GGAAAAGAAAGAAAA | 11124 |
rs138167403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50631488 | TTTAAGTTACCCTTA[C/T]TTTACTTAATAATGG | 11124 |
rs138179655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667931 | CGCTGATGCTCAGAC[A/G]TGATGTGATGTTTAT | 11124 |
rs138201581 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50657574 | AAAACAAAACAAAAC[C/T]CAAAAACTTCAATAG | 11124 |
rs138203708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50899409 | TGCTTGGTAATTTTT[G/T]ATTGGGTCCAAATAC | 11124 |
rs138216279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50809086 | ACAGATCATCAAAGA[C/T]ACAATATATCAGAAA | 11124 |
rs138226090 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50446340 | ACAGGATGAGTATCA[C/G]TAATGTAAAAATCCC | 11124 |
rs138234050 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50790862 | AAACTATAGATTACA[C/G/T]AGTCGACTTGGTGAG | 11124 |
rs138239247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50663048 | TTACGATAAAAGACA[A/G]TTCCTAAAGTGCTAA | 11124 |
rs138240734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50705331 | CCAACAGCATCTTAG[C/G]CATACTGCCCAAGGG | 11124 |
rs138267952 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | FAF1 | GRCh38.p7 | 1:50549735 | AGCTGAGATCCCACC[A/G]CTGCACTTCAGCCTA | 11124 |
rs138271723 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460740 | CCAGACTGAAGTGAT[C/T]CTCCCACCTCACTCT | 11124 |
rs138281157 | snp | A/C/G | 0.0333695 | 0.124785 | intron-variant | FAF1 | GRCh38.p7 | 1:50638476 | TTGAGATGGAGTCAC[A/C/G]CTCTGTTGCTCAGGC | 11124 |
rs138286513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50552169 | AGGCATGGTAGTGTG[C/T]GTTTGTAGTCCCAGC | 11124 |
rs138293857 | in-del | -/T/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640851 | AGTTTATCAGCTGAT[-/T/TT]TTTTTTTTTTTTTTT | 11124 |
rs138308268 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50621476 | GGGATCTCAGCTCAC[C/T]GCAACCTTCGCCTCT | 11124 |
rs138325040 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50537807 | CTGGTTGAAATTTAC[A/G]AAGAAAATCTGGTCA | 11124 |
rs138330557 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50546656 | GGCATGAGATACCGC[A/G]CCCGGCCATTAATTT | 11124 |
rs138361242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50754612 | CTTTCTTTATCTGTA[A/G]TTAAGCATTTGAACC | 11124 |
rs138364069 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50832533 | TATATGAGAGTTTGA[C/T]AAACACTAAATTTAA | 11124 |
rs138368422 | snp | A/G | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50890151 | AATCTTTGTTGGTGT[A/G]AAGTCTGTTTTATCA | 11124 |
rs138411700 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50935039 | TGGTATTCACTAAGC[G/T]TCTTAAATCTGTATA | 11124 |
rs138414307 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50688297 | GTTCCTCAAAAACTT[-/A]AAACACAGAATTACC | 11124 |
rs138420149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941571 | ACTATACTGCCCAGG[C/T]AATACTGAATTCCTG | 11124 |
rs138422027 | snp | A/C | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50887396 | TTAGATCCCATTTGT[A/C]AATTTTGGCTTTGGT | 11124 |
rs138423297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50819988 | CAGATGCATGTGTTG[A/C]CCCATTAGCTAGTAT | 11124 |
rs138428601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50858136 | ACACTAAAAGTTTAA[C/T]ACTTCTAAGCATTTT | 11124 |
rs138433784 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457420 | CTAGAAAAGGTTAAT[C/T]TGCGCACATACACAT | 11124 |
rs138435376 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50729943 | GGAGAGTTGCTTGAA[C/T]CCAGGAGGCAGAGGT | 11124 |
rs138435918 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50606755 | ATCCGCCCACCTCGG[C/T]CTCCCAAAGTGCTGG | 11124 |
rs138443413 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50675853 | AATAAGGTATAAGAG[G/T]CCATTATAGTAGCTG | 11124 |
rs138444756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50592814 | ATGGTGGCACATGCC[G/T]GTAGTCCCTGCTACT | 11124 |
rs138448317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50519528 | AATTTTTGATAGGGG[C/T]GTTTTGCCTATATAT | 11124 |
rs138449095 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50611545 | GCAGATTTTAAAAAT[A/G]AATAAGATGGTCTTT | 11124 |
rs138453648 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50894646 | TAAGACACTAAAAAA[A/C]AAAAATGAAATAATA | 11124 |
rs138458088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50802715 | AAACAAACAACAACA[C/T]AAGCCCAACTTTTCC | 11124 |
rs138484995 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50815657 | TAAACTAATTTACAT[A/T]TCTACCAACAGGGTA | 11124 |
rs138486507 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940687 | ACTAACATAATTATT[C/T]ACAGGTACTTTCAGT | 11124 |
rs138491704 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50724866 | TGGACAAAGCTTACC[A/G/T]TGAGATCTCTAAGCT | 11124 |
rs138495649 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50891176 | AAGCTTGTACATGTG[G/T]CATGTAGTTCTTGTG | 11124 |
rs138504701 | in-del | -/TACA | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50489635 | ATTTGGAGCACATAG[-/TACA]TACATATCCCAAAAA | 11124 |
rs138506854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687480 | ACTGGCCGGGTGCGA[C/T]GGCTCATGCCTGTAA | 11124 |
rs138523025 | in-del | -/TG | 0.16911 | 0.236552 | intron-variant | FAF1 | GRCh38.p7 | 1:50820847 | ATGGCTGAATAATAA[-/TG]TGTGTGTGTGTGTGT | 11124 |
rs138529130 | in-del | -/CC/CTCC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885342 | TCTCTCTCTCTCTCT[-/CC/CTCC]CAATATTTGCTTTAC | 11124 |
rs138531815 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50831711 | CCTTACTTGGAAACA[G/T]GATCTTTGCAGATGG | 11124 |
rs138532669 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50769979 | TCACTTGAACCCGGG[A/T]GGCGGACGTTGCAGT | 11124 |
rs138536915 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50685375 | AACTTTACTGATAAA[C/G]AGTCCGTGTAGCGAG | 11124 |
rs138537372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50679690 | TGAATAAAAGTATAA[A/C]ATTATGTAGTTAAAA | 11124 |
rs138538507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50597174 | AACATTACTTTTTAC[C/T]AGTCTGTGAAGAATA | 11124 |
rs138544025 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50877171 | TACCTTTACAGTGGA[A/G]AAACCTAACAACGCT | 11124 |
rs138557904 | snp | A/C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50661965 | TTTCTGAACAAAAAA[A/C/T]GCTTGAAACCGGATG | 11124 |
rs138567821 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50580179 | TTTGAAGTTTTAATT[A/G]TTTATATTTATTTTA | 11124 |
rs138585618 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50700315 | AGGTTCTTTTCCCCC[-/CT]CTCTCTCTCTCTTCT | 11124 |
rs138588465 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50557465 | AATTACCTGAACACA[A/T]CAGAAACAGGATTCC | 11124 |
rs138592878 | in-del | -/CTTTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50621379 | GAAGTTAGCCCCGAT[-/CTTTC]TTTTTTTCTTTTTTT | 11124 |
rs138625902 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50775391 | TCTGAAACACAAAGG[A/G]TAAGATGTGTTAAAA | 11124 |
rs138631040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50574324 | GCTCTTACAGCAAGT[C/T]ACAGAGAAGCAGGCA | 11124 |
rs138633700 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50650209 | GAATCGTTTGAATCC[A/G]GAAAGCAGAGGCTGC | 11124 |
rs138634218 | in-del | -/T/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50448380 | TGAGACCTTTTTTTT[-/T/TT]GCCTCCCAGAGTTGT | 11124 |
rs138634848 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50737128 | CCAATACAAAAAAAG[A/G]ATCATTATAACTTGG | 11124 |
rs138638489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50483963 | CTGATGTATATGAGA[C/T]ATCTAAGTAGACATG | 11124 |
rs138647833 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50490967 | TTTGGTCTTCCTTTC[G/T]GACCTTTTCTATCTA | 11124 |
rs138651712 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50953839 | AAACAAAAGCACATT[A/T]GTGTGTTACAGAAAA | 11124 |
rs138659146 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50949776 | TTGTCCTCAGTCCCA[C/T]GGCTGCCAAGTGATT | 11124 |
rs138661349 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50879018 | TGGGAGGCCAAGGTG[A/G]GCAGATCACTTGAGG | 11124 |
rs138664153 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50883900 | GAGGGTGAGGCAGGC[A/G]GATCACCTGAGGTGA | 11124 |
rs138672246 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50782147 | TTCACTATACTATAC[C/T]TTTTATTGTTATTTT | 11124 |
rs138687587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541977 | TACAAAGCATGTTTG[C/T]GGTGCAGATCGCAAA | 11124 |
rs138688315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570310 | TTTTCCACAAGGAAA[C/G]TTTAGGAAAGTGTTT | 11124 |
rs138692094 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50478727 | TTATTTCCAAAACTT[C/T]TTCATCACCCAGATA | 11124 |
rs138700768 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624038 | AAGAAGAAAGAAGAA[A/G]AAGAACCACAAATAC | 11124 |
rs138704662 | snp | A/G | 0.117886 | 0.21224 | intron-variant | FAF1 | GRCh38.p7 | 1:50759601 | ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG | 11124 |
rs138705001 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50541413 | AAGGTGCTCAAGCAG[C/G]CTAACCTTCTATGCC | 11124 |
rs138707594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909539 | GATTTGGTCTTTTCA[C/T]ATAGTCCCATATTTC | 11124 |
rs138712851 | in-del | -/GTGA | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50480170 | TTCTACTAAAAATAT[-/GTGA]GTATTTAAAGCATAT | 11124 |
rs138714168 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50890460 | TCTTCCTAGCATTGA[C/T]GGTCTTTACAATTTG | 11124 |
rs138714984 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50487453 | ATCTACTCTTTCTTA[A/C]TCCCTTTGAATTGCA | 11124 |
rs138724118 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50913559 | AGTTTTACAAAGACT[C/T]GAATTGTTTTCAAAT | 11124 |
rs138727527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50796856 | TTGGGTAGACCAGGT[A/G]AGGTGGCTCACACCT | 11124 |
rs138729305 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50675480 | CTATCCAAAGAGGCA[C/G]ATGCTGCTCCAGACT | 11124 |
rs138740256 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50825902 | CTTGAAAATCAAGCA[G/T]TATACCTCAAAATAA | 11124 |
rs138754336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465971 | AGTTAGATCGAGAAA[A/G]GCCTTTCACTCTGAA | 11124 |
rs138754692 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692251 | TTTACTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 11124 |
rs138755621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816496 | GGCGTGAGCCACCAC[A/G]CCTGGCTTTTGCCCA | 11124 |
rs138793023 | in-del | -/GG | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50781139 | AGTCAATACTCCTCC[-/GG]GTGCCCCGGTGAGGG | 11124 |
rs138793169 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50740158 | TTGAGTAGGAATAAA[-/T]AAGTAACCCTATATA | 11124 |
rs138805532 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50492288 | GTAATCCCTGGGTCA[C/G]TGTAGAAAGAGGCCA | 11124 |
rs138816489 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50855194 | CAGATCAGAGATCAT[G/T]TGTCTTATTGATTTT | 11124 |
rs138825162 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50622095 | ACTTGAATTCGGGAG[G/T]TGGAGGTTGCAGTGA | 11124 |
rs138832278 | snp | C/T | 3.30846e-05 | 0.00406709 | intron-variant | FAF1 | GRCh38.p7 | 1:50744666 | TTTCTTTTATTTCTA[C/T]GCAATTAAGAAACTC | 11124 |
rs138864991 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50581637 | AAGAGATAAGCAGAG[C/G]GTTTTTCACTGGGAA | 11124 |
rs138874058 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50548352 | GAAGTCAGGGAGAAC[A/T]TGATGTTGTAAGGTG | 11124 |
rs138905171 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50680449 | GAACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 11124 |
rs138906706 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50702673 | ACCCTCAATAACTAA[A/C]TGGCTTAAATTAAAA | 11124 |
rs138907261 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50597841 | AAAAGTAATCCATGG[A/G]AAAGGCAGGCACTTA | 11124 |
rs138907701 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50714403 | CTGTAATCCCAGCTA[C/T]GCAGGAGGCTGAGGC | 11124 |
rs138912636 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470920 | TTTATAATACTTTCC[A/G]TTATCACAGCCTGCT | 11124 |
rs138919673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50934584 | AAAAAATTAGCCAAG[C/T]ATGGTGGTGCACACC | 11124 |
rs138926590 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | FAF1 | GRCh38.p7 | 1:50814275 | TTATAGCTGCATATT[A/G]TATGTACAGTATACA | 11124 |
rs138929062 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50563986 | TTCCAATTTGTTAGA[G/T]AAATTAGGAAATTTA | 11124 |
rs138929118 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50615416 | TGTTGGGTTGAATGG[G/T]AGCTCTGATTTAAGT | 11124 |
rs138929786 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50893539 | CCAAACAAATGGAGA[-/CT]CTCTCTCTCTCTCTC | 11124 |
rs138936490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50514908 | AACCTAGGATGGAGC[C/T]TGTACATTTTTCAAG | 11124 |
rs138961606 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50895933 | TATGACAAACCCACA[A/G]CTAGCATCATACTGA | 11124 |
rs138974356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694949 | CTTTGGCGACAGAGC[A/G]AGACTGTCTCAAAAA | 11124 |
rs138974399 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50749285 | AAGACCTGACACCAC[C/T]TTCTTACACTCTTGA | 11124 |
rs138979082 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510537 | CCATTAGTCCCTAAC[C/T]GACTGTTACACCCCA | 11124 |
rs138979795 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50648088 | ACATAGTGAAACCCC[A/G]TCTCTACTAATAATA | 11124 |
rs139000074 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50849965 | CAACAATACACATTC[G/T]CTTTAAATGCAGAAT | 11124 |
rs139006724 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50755391 | CACATCTAGGTCACA[C/T]TGATGCAAGAGGTGG | 11124 |
rs139009691 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50891833 | AGGAGGCAGTCTGTC[C/T]GTTCTCAGATCTCAA | 11124 |
rs139014048 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50507728 | CTTAAAAAAGAAAAA[A/G]GGTAAGAACTTGTCT | 11124 |
rs139014114 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50452824 | TAGCACTGCATGTGT[A/G]CTCTTGAGTAAGTCA | 11124 |
rs139042679 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677356 | TATTAAAATAAAATT[C/T]ATGTACCCTTCAACC | 11124 |
rs139042974 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50760490 | ATAACAAACTGTCTC[A/T]CAGACCACGGTGCAA | 11124 |
rs139054497 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50598267 | TGCCACTGTACTCCA[C/G]CTTGGGTGACAGAGT | 11124 |
rs139060560 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50511572 | CCCCTGAAAAGGACA[C/T]GAACTCATCCTTTTT | 11124 |
rs139063802 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50592433 | CAGAAATATGGAAAA[A/C]TCATTAAACGGGGGC | 11124 |
rs139080073 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50503650 | TGCTAAAACCAAAAC[A/C]AAAAAAAAAGTAACA | 11124 |
rs139091435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50494456 | GAAATTTTTACACAT[C/T]GATTGGGTGGAGGTA | 11124 |
rs139104256 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50783107 | CAACAAATTAGATAA[C/T]ATAGAAGAAATGGAT | 11124 |
rs139107899 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50842274 | TGCAGCCCAAATGGT[A/G]TAAGGGAGGTAGGTA | 11124 |
rs139117573 | snp | C/G/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50627703 | GGGAATGTGAGGGGG[C/G/T]GCTTCTGGGATACTT | 11124 |
rs139118855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50593003 | ATGTAGGAGTAGAAC[C/T]GGAAGACAGCAGTAG | 11124 |
rs139121081 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50506263 | AGGTAATGACTCTAA[C/T]GAACACCTAATCTTA | 11124 |
rs139154781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50599583 | TCAGTAAAAATTATT[A/C]AGTAATTTAATTTAT | 11124 |
rs139155926 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50923670 | TGAACATAGATTCGA[C/T]AGAATCCTCAACAAA | 11124 |
rs139158190 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50455556 | TTTTGTTCTAGTTTT[C/T]GGAAGAGAGTTGTCA | 11124 |
rs139159036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930881 | GCAATATAACTTAAC[C/T]AGGGTTAGAAAGCAG | 11124 |
rs139166904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50473455 | GAAGGGCAAACTTAG[C/T]TCCTAAGTTTTTTAA | 11124 |
rs139168720 | in-del | -/T | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50484318 | ATTTTTGCTTGCTTC[-/T]GGATATAAAGAACAG | 11124 |
rs139171518 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50837944 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 11124 |
rs139183458 | snp | C/T | 0.00319488 | 0.0398401 | intron-variant | FAF1 | GRCh38.p7 | 1:50818113 | ATCTGTCAAAACTTA[C/T]CAAATTTTACAGTGG | 11124 |
rs139205440 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50457803 | CAGCTACTGGGGAGG[C/T]TGAGGCTGCTGTGAT | 11124 |
rs139217450 | in-del | -/GGACCCAGC | 0.198324 | 0.244601 | intron-variant | FAF1 | GRCh38.p7 | 1:50939618 | GTTCTCAAGGGGAAT[-/GGACCCAGC]TTTTGCCCATTAAGT | 11124 |
rs139218284 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929099 | AAAAAAGAAAGAAAA[A/G]AAAAAAAAACTGGGA | 11124 |
rs139223364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927335 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 11124 |
rs139243470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50959658 | CGCACCGTATAAAAG[C/G]CTAAATGACACACCA | 11124 |
rs139244188 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50763036 | CAAGGCAGGTGATCA[C/T]CTGAGGTCAGGAGTT | 11124 |
rs139259314 | in-del | -/AGGC | 0.0726307 | 0.176182 | intron-variant | FAF1 | GRCh38.p7 | 1:50694293 | ATTTTCATTAGGCAA[-/AGGC]AGGCAGGCATGTAAA | 11124 |
rs139293519 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50771389 | CAATAAAGGTCTAAT[A/G]TCCAGAATCTATAAG | 11124 |
rs139298043 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50765772 | CTGTTACCACTTTGT[A/G]AAATTTAAAATATCA | 11124 |
rs139300993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50571620 | TCCTACTGGCAATAG[A/T]GTCTGGGATGCTTAT | 11124 |
rs139308966 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561848 | GGATGGACGGATGGA[A/C/T]GGAAGGAAGGAAGGA | 11124 |
rs139315033 | snp | A/C/G | 0.0334187 | 0.12516 | intron-variant | FAF1 | GRCh38.p7 | 1:50915142 | TTGGAAGGCTGAGGC[A/C/G]GACAGATCACCTGAG | 11124 |
rs139335419 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50622488 | CTCTCGGTAGAAGTG[A/G]CACTTCCAGGCCGCA | 11124 |
rs139337219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50588223 | ACGTGGGAGATGGAA[A/G]TTGCAGTACGTGCCA | 11124 |
rs139347509 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50636744 | TTTTTCCTCTTAGGA[A/G]CTTTTAGTGTCCTCT | 11124 |
rs139358657 | snp | C/T | 3.30956e-05 | 0.00406776 | missense | FAF1 | GRCh38.p7 | 1:50567147 | TCAGATAAGAAACAA[C/T]GGATTCAGCACAAAG | 11124 |
rs139385998 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50639007 | TTACTCCTTGGCAAC[C/T]CACTGACTGGATTTC | 11124 |
rs139391035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50768054 | CCAAAAAGAGAACCA[C/T]CACATGTGCAATGAC | 11124 |
rs139391131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721278 | ACTCTTATCACCAGC[A/G]ATCTCTGCTCGCTGC | 11124 |
rs139392983 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50691393 | GACTGCAGGCATGCA[A/C]CACAATGTCCACTTC | 11124 |
rs139406957 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50577250 | TCCCCCTAGGCTGGG[C/T]GCGGTAGCTCATGCC | 11124 |
rs139407154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488642 | GTGGACACAATGATA[C/T]AGGGTTTTGTACTGG | 11124 |
rs139428992 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50833704 | AGAGGCCCACCAAGA[C/G]TAGACTCATTAGAAC | 11124 |
rs139431367 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50942484 | GAGGGGAAAGGGAAG[A/G]GAAGGGAATTAAATG | 11124 |
rs139438406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50590306 | TTTCCATTTATTTAT[A/G]TCTTCTTTAATTTTT | 11124 |
rs139440820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770841 | AAGCTGGAGGCACCA[C/T]ATTACCCAACTTCAA | 11124 |
rs139442663 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | FAF1 | GRCh38.p7 | 1:50722618 | CGCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 11124 |
rs139448656 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463398 | ACAAGTGTGATTATA[A/T]GCTGAGTCCTGTGAG | 11124 |
rs139449144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871611 | CTTTACCATATGGGT[G/T]ACTCAATATTTTAAC | 11124 |
rs139450168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858520 | GGCTCAACTGAGTTA[A/G]GATGTGCTATAAGTA | 11124 |
rs139451119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50634433 | GACTTATTAAGAAAT[C/G]GTATCACATATGTTA | 11124 |
rs139453617 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50931338 | ATCTGCATTCTTTAG[A/G]GTTGAGCATATGTAT | 11124 |
rs139462546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846694 | AACCACAACTGTTGA[A/G]AGCATGATGGAGCAC | 11124 |
rs139464190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50617022 | CTTGCTAAATTGTCT[A/G]TCAGTTCTAGGAGCT | 11124 |
rs139473083 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FAF1 | GRCh38.p7 | 1:50603200 | TAATTAAAACAGCTA[C/T]TCCTAGATACCATCC | 11124 |
rs139478849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534407 | TGCCTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11124 |
rs139480445 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50474454 | TTTTGGGGAACAGGT[A/G]TTTGGTTACATGAGT | 11124 |
rs139481340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516204 | CACCAACTTACAGTT[A/C]TCTCTCATGAGTCAT | 11124 |
rs139497033 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50936816 | AGAAGAAATATGAGG[A/G]GAAGGAGAGAGAAAC | 11124 |
rs139500832 | in-del | -/A | 0.437118 | 0.165792 | intron-variant | FAF1 | GRCh38.p7 | 1:50645834 | AAAAGAAAAAAAAAA[-/A]GGAAGAAAAAAAATA | 11124 |
rs139530180 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50613518 | AATCCAAATGTCATT[C/T]AGCTCTACGTTGTAA | 11124 |
rs139534127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50792561 | GATGAGATGCCTGAA[C/T]CTTCCTAGCATAATG | 11124 |
rs139541130 | snp | A/C | 0.0264357 | 0.111888 | intron-variant | FAF1 | GRCh38.p7 | 1:50583397 | TCCTTTGGGAATATA[A/C]TAAAAATATTAAATT | 11124 |
rs139542805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50721771 | TAGGACTACAGGCAC[A/G]TGCCACTATGCCTGG | 11124 |
rs139545864 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50528949 | AACATTTTATTTCTC[C/T]AGTTCACTTTATTAA | 11124 |
rs139572772 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50873664 | CACTCCTTTTCTAGG[C/G]ATTTCTGAAAAACCT | 11124 |
rs139572900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639068 | TCATAAATGTGGAAT[C/G]ACACAGTGATGTAGT | 11124 |
rs139582543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521885 | AATGTGGAGGGCTGG[C/T]TCTGAACAGGTGTGC | 11124 |
rs139590428 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | FAF1 | GRCh38.p7 | 1:50905286 | TAATCCAGTCTATCA[C/T]TGATGGACATTTGGG | 11124 |
rs139595903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50805453 | ATACAGTGGAAGCCA[A/G]TGTCAGAGATGACCA | 11124 |
rs139596706 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50863575 | TAAATGAAACAAAAA[G/T]CTGCTTCTTTGAAAA | 11124 |
rs139603682 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50764627 | TTCCCATTTCTCATG[A/T]ATCATAGGCCTACGC | 11124 |
rs139607680 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50717398 | TTGGGAGGACACAAT[A/G]AGAAGGTGACAAAGC | 11124 |
rs139622183 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50516759 | AACAGTAATTAGATA[G/T]CTACAGCTATACATT | 11124 |
rs139623062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50947120 | CTAGAAGTTACTGCT[A/G]TTACTCTTTCCCTAT | 11124 |
rs139626367 | in-del | -/AACTTTTTCCACAG | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50691148 | GTTGAGGAACTATCA[-/AACTTTTTCCACAG]CTACTACATTATGTC | 11124 |
rs139669408 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50659373 | AGAGGGAAGTGAGAA[A/G]GAGAGGGGGAAGGAC | 11124 |
rs139687015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50792271 | AAAGTTTCTTACTTG[C/T]AACCATAGGTACAAC | 11124 |
rs139692630 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50887986 | TATGGCCATTTTCAC[A/G]ATATTGATTCTTCCT | 11124 |
rs139695792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565428 | ATAGCTCTAAAGCCT[C/T]AAACAACACCTTTAT | 11124 |
rs139717692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852855 | AATAAACCCTCAATT[A/C]AAGAAGAGACAATAG | 11124 |
rs139728820 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50821861 | CAAAGAATGAAAACA[C/G]TATAAAGAAGTAGAT | 11124 |
rs139737290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50731871 | CATGGGGGATTTGGG[A/G]TATATGTTTTTATTA | 11124 |
rs139739501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50746861 | GACCCAGGGCCTCAC[A/C]ACCCTGCACAGACGC | 11124 |
rs139750618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660357 | ACCATTCCTTGTGAG[C/G]TAAATATCTATCAAA | 11124 |
rs139764105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50521225 | CAACCAGTAGTAGTC[C/T]CTCAGTTTAGTAGTA | 11124 |
rs139769004 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50612747 | AGTCTGAATTAACTA[C/T]ACCATGTTAGGCACA | 11124 |
rs139773059 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50796993 | ATAAAAAAATTAGCC[A/G]GGCTTGGTGGCACAT | 11124 |
rs139773756 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766790 | CAAACAAGCAAGCAA[-/G]CAAAAAAAAAAAAAA | 11124 |
rs139774564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50528627 | ACTGGAGTTCCTTGA[A/G]TTATTTCTATACTAA | 11124 |
rs139775217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742093 | GCAGGAGGACTGCAT[C/G]AGTCCAGGAATTCAG | 11124 |
rs139786612 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50656193 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGGTGCCT | 11124 |
rs139789947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50552896 | TTATTGTGTGCTTAT[C/T]TGAAGCTTGTGTTTA | 11124 |
rs139791048 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50638733 | ACAGGCATGAGCCAC[C/G]ACGCCCAGCCTAGCT | 11124 |
rs139791650 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50501736 | GGAACTCTCTTATAC[A/T]CTGCTGTTGGGAACG | 11124 |
rs139792208 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50880703 | TTTCTGTTGTTTAAG[G/T]CACCCAGTGTACGAT | 11124 |
rs139823347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549220 | GAGATTTAAAGTATA[C/T]GTATCTCTACTTTAA | 11124 |
rs139830344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50583061 | GAATTCCAATAGAAG[A/G]AAAAAACTGTTTCTT | 11124 |
rs139855524 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50815608 | GTTCTTTTTAAGTTC[-/T]TTGAGAAATCTCTAA | 11124 |
rs139859900 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50925993 | GGCTGAGGCAGGAGG[G/T]TCGCTTAAGGCCAGG | 11124 |
rs139863579 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50505122 | GGGATGTTATTTTTG[A/C]TTTCAGGAAAGACAT | 11124 |
rs139865151 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50884928 | GCTGGCAGATTTTTC[A/G]TTACACCTTCGATCA | 11124 |
rs139866078 | in-del | -/CAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50715959 | TATTGATAAAATCAT[-/CAA]CAACACAAAGAAAAT | 11124 |
rs139876701 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50888671 | TGGATTACGTTTACT[A/G]ATTTGCGTATGTCGA | 11124 |
rs139877722 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922290 | CTGGCAAAACCCTGT[C/T]TAAACTAAAAATACA | 11124 |
rs139878228 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50778838 | AAACAAAACACACAG[-/AC]ACACACACACACACA | 11124 |
rs139886517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50716722 | CCGTAAAAACACGCC[A/C]ATCAGTGCTGTGTGC | 11124 |
rs139890165 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50803596 | AAGGAATTAATAATA[A/G]AGGAATACAAAGAAA | 11124 |
rs139913505 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50818956 | ATACAATATTTTAAA[C/T]AATTTTTTGCATTAA | 11124 |
rs139924977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50727890 | TTGCCAGGAGCTCTC[A/G]GACCTTTGGCCACAG | 11124 |
rs139936069 | in-del | -/CA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50700243 | CTTTGAAAAGGGGGC[-/CA]TGTGTGTAATGGGTC | 11124 |
rs139937761 | in-del | -/TTTA | 0.0399052 | 0.1355 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961015 | TATAGTCAGTCTATT[-/TTTA]TTTATTTATTTATTT | 11124 |
rs139939155 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950996 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGACCA | 11124 |
rs139941578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50740681 | CCAATCCACTAATGG[A/T]TTATGGTCCATAGTT | 11124 |
rs139953889 | in-del | -/AAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624030 | GAAGAAGAAAGAAGA[-/AAG]AAGAAGAAGAACCAC | 11124 |
rs139958105 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50685976 | ATGCTTTCCTAACAG[A/G]CTAATTAATATCTTT | 11124 |
rs139958909 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739281 | GTACATGTGCATACA[C/T]ATACATATGTACATG | 11124 |
rs139977218 | snp | C/T | 0.131723 | 0.220251 | intron-variant | FAF1 | GRCh38.p7 | 1:50534482 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAAGCTA | 11124 |
rs139986095 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50821409 | AGATAGTTTTTAGCA[C/T]ACATATTAAAGGAAC | 11124 |
rs139997175 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50677936 | CAACTAGTTTTTATC[A/G]AATTATGCAGTTCTT | 11124 |
rs140004010 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50576501 | AGATTTTTATTCCTG[C/T]TGATTTTTAGTTACT | 11124 |
rs140005244 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50886077 | AGTTATTTTTGATCA[G/T]TTCATATTTTAGTCC | 11124 |
rs140010442 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847889 | CAAATGCACACATAT[-/AC]ACACACACACACACA | 11124 |
rs140024044 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50785418 | ATACAGAAAAACTTC[C/T]ATAACTCAACAATAA | 11124 |
rs140027012 | snp | A/G | 0.00380587 | 0.0434563 | missense | FAF1 | GRCh38.p7 | 1:50738885 | GACTAGATGATGAAG[A/G]TGGTGGCAAATCTGG | 11124 |
rs140034934 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50573378 | TGCTGAGATTACAGG[C/T]GTAAGCCACTGTGCC | 11124 |
rs140040903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50539401 | CAATTTTATTAAGAT[A/G]TTTCTTTTAGATTTT | 11124 |
rs140054682 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50447405 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 11124 |
rs140087721 | snp | C/T | 0.110872 | 0.20771 | intron-variant | FAF1 | GRCh38.p7 | 1:50908467 | GTCTAATGTTGATAG[C/T]GGGGTGTTAAAGTCT | 11124 |
rs140103936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534909 | TAAGGAAGCTGAGAA[A/T]TTCAGAATGCTGGAG | 11124 |
rs140105935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50589346 | TGAAAAATACGAAGT[C/T]TGCTGAGGAGGGATT | 11124 |
rs140117211 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50484658 | TGGACAAAAGCAACT[G/T]ACATAAGATAAAAAT | 11124 |
rs140134347 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50747103 | GGACAGTGCAGAGAA[A/G]AAATGTGAGGTTGGA | 11124 |
rs140145002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881631 | TAAGTTGAAAGTATC[A/C]ATCGGGAAGACCCTT | 11124 |
rs140150203 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50734499 | CAGCACTTTGGGAAG[C/T]CGAGGCGGGTGGATC | 11124 |
rs140152043 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50824260 | GGCTTATCCATTCCA[A/G]TAGGCACCAAGCCCA | 11124 |
rs140158306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50699953 | ATTTGATTCATCCTC[A/G]GACACAAAGCTTCAC | 11124 |
rs140172049 | snp | C/T | 0.118933 | 0.212888 | intron-variant | FAF1 | GRCh38.p7 | 1:50706941 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11124 |
rs140185861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50542830 | GGCCAAATGCTAAAA[C/T]TACAAATTTGAAAAG | 11124 |
rs140193989 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50453134 | CAATGAAAGACGTGG[C/G]TGGAAAGACAGTTTG | 11124 |
rs140198469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50844804 | ATTATAAAGGGGCTG[C/T]CAGTGATTGGTAATC | 11124 |
rs140204530 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50698752 | TATAACTTACATTTC[A/T]ATGAGCACTCCCAAA | 11124 |
rs140205173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955995 | GGCTGAGGAGAGAGG[A/G]ATATAAGGACTTATT | 11124 |
rs140205689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50751341 | CTATTTGTTTGATTG[A/T]TTGTTTGTTTTGAGA | 11124 |
rs140210508 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50921296 | GCTGGCCTGCCCAAC[C/T]CTGCAACGCACTATC | 11124 |
rs140222545 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50748004 | ATAGCCTGCAGAACT[A/G]CGAACCAATTAAACC | 11124 |
rs140226996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50922391 | TTGAACCTGAGAAAC[A/G]GAGGTTGTAGTGAAC | 11124 |
rs140235143 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573817 | TCAGAGGGTTAAAAA[A/C]AAAAAAAAAAAAAAC | 11124 |
rs140248614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451146 | CTGCAAAGCATAGGT[A/G]TCGAGGACATTTTCT | 11124 |
rs140249347 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50549499 | AAAACAAAATTTAAG[G/T]CTGGGCATGGTGGCT | 11124 |
rs140256221 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50831863 | TGTGAAGGGTGGTAA[C/T]GTGAGCCACTCCCCA | 11124 |
rs140259851 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927872 | TCTCTATGTGCCCTA[A/C]TCTCCTCTTTTTCTT | 11124 |
rs140260657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50917300 | AGAGGCAACAAGAAC[A/G]AGATGGTATAAGATC | 11124 |
rs140262197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459452 | CAGACTCAACAAATC[C/T]CAAAGTGAACCTGCC | 11124 |
rs140264335 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50786359 | ATAAGCCATCACAGC[A/G]GGCAAATACTGCATT | 11124 |
rs140269035 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50648219 | GCCGAGATCGTGCCA[C/T]TGCACTCCAGCCTGG | 11124 |
rs140273958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50898609 | TCTGTAATGTTTCCT[A/G]TAGAAGGGAGAGAAT | 11124 |
rs140289895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50811613 | TAGGAAGAATCAATA[C/T]TGTGAAAATGGCCAC | 11124 |
rs140295343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807569 | GTCCCTCCCCCAACA[C/T]TGGGAATTACAATTC | 11124 |
rs140296266 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50903923 | CACAAAACAAGCTAC[A/G]TACATGAAAACTGTA | 11124 |
rs140298602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50780528 | CCTGGGTACGGAAAC[C/T]AATGATCTTTGACTT | 11124 |
rs140302676 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50693727 | AAGTAATACCTTAAG[A/G]ATTAAAAGATTACTT | 11124 |
rs140316475 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50495619 | CCCTCCTTTTGGGTA[C/T]ATACCCAGCAGTGGG | 11124 |
rs140342328 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50629599 | TTATGGTATAGTAAA[A/C]AGAGGTAGCCTTTAG | 11124 |
rs140379596 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50627846 | AACATTTTTTTTTTT[-/T]AAATGCTGCTAAGAA | 11124 |
rs140387829 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50623062 | TGACCCTGTTCTCAC[C/T]GGTTCCCAACTTTAC | 11124 |
rs140388774 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50591255 | CTTGCTTGCACTAGT[A/G]CAACAGACTCATACC | 11124 |
rs140390927 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50501868 | TAGTTACCCAAGACA[A/T]ATGACCATATTACCA | 11124 |
rs140392832 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50444171 | AAACCTAGGGGGATG[C/T]AGGACATCATGTTTC | 11124 |
rs140393662 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50540064 | GAAACCCCCGCCTCC[C/T]GGGTTCAAGCAATTT | 11124 |
rs140395165 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50887095 | TGTGAGATGGTATCT[C/G]ATTGTGGTTTTGATT | 11124 |
rs140400468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50789028 | TTGTAGAAACGGAGT[A/C]TTGTTAATGTTGCCC | 11124 |
rs140420828 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50513084 | TGTGAGGATCAAATG[G/T]AAAACCAGATGGTGG | 11124 |
rs140438824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893339 | CCTTGGGAAGACTTT[C/G]CAGGTATTGGAAAGA | 11124 |
rs140439508 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50671222 | TCAGCCTGGCCAACA[C/T]TGTGAAACCTCATCT | 11124 |
rs140444850 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50762136 | CCAACTTACAAGGGA[C/T]GTGAAGGACCTCTTC | 11124 |
rs140449808 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50679420 | TAACCCTATTAAATA[C/G]ATGGCATTATTTCTA | 11124 |
rs140453220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50560798 | TCCTATTCAGAACAA[A/G]AGATACCCACTAACC | 11124 |
rs140454193 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50586569 | AGATACATTTGTTGC[A/C]TGAATAAATAAATGG | 11124 |
rs140464158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50559663 | ACATTCTGTTAAGAC[C/T]GCCACTAAAAATCAA | 11124 |
rs140468540 | snp | C/T | 0.112631 | 0.208878 | intron-variant | FAF1 | GRCh38.p7 | 1:50909092 | CAAAATCTCTCAGCA[C/T]TTGCTTGTCTGTAAG | 11124 |
rs140473037 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50944640 | ACCATACAGAGACTC[A/G]GCAAGCAGTATACTC | 11124 |
rs140490418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50860076 | GAATGACACTAGACC[C/T]CTACTTTTCACCATA | 11124 |
rs140491415 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50937183 | GTATTACTATTAATT[A/G]TGCATTAATAATAAT | 11124 |
rs140506622 | snp | A/G | 6.75049e-05 | 0.00580929 | missense | FAF1 | GRCh38.p7 | 1:50738953 | AGAGATTTTAGGACC[A/G]TCTGAAAAAGAAAAA | 11124 |
rs140522171 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50630407 | CATAGGTAAGAACTA[C/T]GATAGCATTTTTGAA | 11124 |
rs140529843 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50555949 | GTATATATACATGGT[A/G]TATATATATGGTATG | 11124 |
rs140536720 | in-del | -/A | 0.131723 | 0.220251 | intron-variant | FAF1 | GRCh38.p7 | 1:50607517 | TTTGCTCAATGATCC[-/A]AAAATGTGCCTTGCA | 11124 |
rs140543038 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469557 | ATGGTAAGGAGTTTG[G/T]ACTTTTTCTGCAGGC | 11124 |
rs140546895 | snp | A/G | 0.00030175 | 0.0122794 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50583705 | TCCTTCATTTTCTGC[A/G]TTTTCTGGCACTAAA | 11124 |
rs140557224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855853 | ATAGCCTGATGTTTT[C/T]GCTTGGGCCTGATAC | 11124 |
rs140559835 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | FAF1 | GRCh38.p7 | 1:50568668 | TGAGGTTTAGAAAGC[A/G]GACTTGTCCCAAATG | 11124 |
rs140562672 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50806351 | GTTAAATTAAATCAG[A/T]TAATACAAGTATTAG | 11124 |
rs140563344 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50939045 | GAATGCTTTGGCTAT[C/T]TGGGCTCATTTTTGC | 11124 |
rs140565484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50812928 | CCTTTGCAGCAACAC[A/G]GATGGTGCTGGAGGC | 11124 |
rs140568271 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50946101 | ATAAGACATTATGCA[C/T]TCCATCTCTCAGGCA | 11124 |
rs140571912 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50897635 | AAAGTCGACCTAAAA[A/T]CATTTCTAATTTTAT | 11124 |
rs140586796 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50723538 | AACAGGGAGAGAGGA[C/G]AGTAGAGTGGCTAGA | 11124 |
rs140610998 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50472999 | TGGAATCTGGGTGGG[C/G]CTAGAGCATCTGTTC | 11124 |
rs140617625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808260 | AGAACTCCTTAAGGG[A/T]GTGCTAAATATGGAA | 11124 |
rs140630592 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50720505 | CTTAAAATACTTTTA[C/T]GGATAAATATTGACG | 11124 |
rs140640601 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519398 | GGAGGGAGGGAGGGA[A/G]GGAGGGAGGGAGGGA | 11124 |
rs140664261 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50652271 | TATAGTAATTAGACT[A/G]CATGACAACTCTTTG | 11124 |
rs140704216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610732 | AGTTCAAGAGAGCCC[A/G]TGGGAAGCCACACCC | 11124 |
rs140705261 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50833192 | CTTCAAATGCCAATT[C/G]CAAGTATTAGGTCCC | 11124 |
rs140713080 | in-del | -/T | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50858092 | AATATGTAATTTAAA[-/T]TTCAAATAGGTATAT | 11124 |
rs140713515 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50523808 | TGATGGGCATTTAGG[C/T]TGATTCCATGTCTTT | 11124 |
rs140759992 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656825 | GAGGCAGAGGCTGCA[G/T]TGAGCTGAGATCGTG | 11124 |
rs140770493 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50574139 | TAAAAAAAGAAAAGC[C/T]TAAAGTAAAATCAAA | 11124 |
rs140775338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50449294 | TTCTTATGCACAGTC[A/G]TACAACCAGAAATTG | 11124 |
rs140777613 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50916669 | ATGAAAGGAGAGGAG[C/G]ACTAACAAATCATAG | 11124 |
rs140778257 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50886928 | CAAATGGTATTTCTA[C/G]TTCTAGATCCTTGAG | 11124 |
rs140801555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50645701 | GGTGGCACCTGCCTG[C/T]AGTCCCAGCTACTCT | 11124 |
rs140807898 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50560276 | GTGCTTTAAGTCAAT[C/T]AACTCTTGCCAAAGA | 11124 |
rs140809139 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50506897 | TAGCCTTTGCGAGGT[A/C]AATGTTCTTGCTTTA | 11124 |
rs140817113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50853402 | TACAAAATTATCTTC[A/G]AGGACTAAAAATTCC | 11124 |
rs140822830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50758440 | CTAGTTCCCTTTCCT[A/G]TTCTTCATGTTATTG | 11124 |
rs140827856 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50956518 | TCTCAAACTATTATT[A/G]AGTCTCACAATCATA | 11124 |
rs140844812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778175 | TAAACACAGTATACA[A/G]TGTATGATTTCAATT | 11124 |
rs140862931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50781030 | CTGGCCACTGTGGGT[C/G]ACAGCCTGATTGAAC | 11124 |
rs140865715 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50690854 | GGCTTTTTGTGTTTA[A/G]TTTCTTTCATTTAGC | 11124 |
rs140866275 | in-del | -/GACAGAG | 0.372995 | 0.217652 | intron-variant | FAF1 | GRCh38.p7 | 1:50957372 | TTTTTTTTTTTTTGA[-/GACAGAG]TCTCGCTCTGTCGCC | 11124 |
rs140871242 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50579809 | AGGTATTTAAGATAT[C/G]TAATACTCAAATATA | 11124 |
rs140872563 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50742541 | GGTGTGCACCACCAC[A/G]CCCAGCTAATTTTTA | 11124 |
rs140872808 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50607246 | TGTGGTATGATTCCA[A/G]GTGTGTAAATACTTG | 11124 |
rs140872840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50687172 | AAGTGGCATAATTCC[C/T]GATTCTCTAGTTTTC | 11124 |
rs140878407 | snp | A/G | 0.000330126 | 0.0128434 | intron-variant | FAF1 | GRCh38.p7 | 1:50490715 | CACATACTTGTTTAC[A/G]AAGAAAGAGAGAAAT | 11124 |
rs140885649 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50922708 | CTATAATCCCAGCTA[C/T]TTGTGGGGGCTGAGG | 11124 |
rs140893315 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50836320 | GGTATAATAGCATGA[A/G]TCACCATGCCCAGCC | 11124 |
rs140904320 | snp | G/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50623462 | TAGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 11124 |
rs140909239 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | FAF1 | GRCh38.p7 | 1:50955607 | ATTAAAAATAGAATG[A/C]CTATGTGATCCAGCA | 11124 |
rs140912765 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465524 | TGTCCTAGGTGCCAG[G/T]AATGTATTAGTTAAC | 11124 |
rs140921630 | snp | A/G | 0.11963 | 0.213316 | intron-variant | FAF1 | GRCh38.p7 | 1:50830221 | CTCCTGGATTCAAGC[A/G]ATTCTGCTGCCTCAG | 11124 |
rs140926493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848846 | CAGCACAAGTTGGGA[C/G]AGGCTACAGAGACGT | 11124 |
rs140930161 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50723916 | ACCACACCTGGCTAA[A/T]TTTTGTATTTTTAGT | 11124 |
rs140934767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626722 | TCTCTTTTAAAAAGT[A/G]TTATTCTGATATAGT | 11124 |
rs140938175 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739368 | TGTACATGTGTACAC[A/G]TACATACATATACAT | 11124 |
rs140945602 | in-del | -/TAAA | 0.494272 | 0.053207 | intron-variant | FAF1 | GRCh38.p7 | 1:50882601 | AGCAAGACTCTGTCT[-/TAAA]TAAATAAATAAATAA | 11124 |
rs140946020 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50605356 | AAATACTTCTGAAGA[A/G]CATTAAGTTACACAA | 11124 |
rs140961504 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50540859 | AGGCAAAACAGTGGA[A/T]ATTCTGGGGACTAGC | 11124 |
rs140961804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50947642 | AATTCAGCAGCAGCA[C/T]TCAAATTTTACAAAG | 11124 |
rs140969572 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50451544 | TAACCACCACAGTAG[A/G]TTATTTTAGTATTGT | 11124 |
rs140982992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50915490 | GTCAACCACTTAGAC[A/G]AGTAGAAGATAAAAC | 11124 |
rs141003499 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50491681 | ATTTAAATAATGAAC[A/C]ATTGAGTTCTTTATC | 11124 |
rs141007439 | in-del | -/TTAT | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50930963 | AGTCTTAGTCTAACA[-/TTAT]TAATTAATTACAGCA | 11124 |
rs141010592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50592203 | CATCTGACTAGTACA[C/T]AGTGAGCATTCAATA | 11124 |
rs141021155 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50673032 | GGAGGCTGAAGCAGG[C/T]GGATTACCTGAGGTC | 11124 |
rs141048494 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FAF1 | GRCh38.p7 | 1:50642111 | ATGAGGCTGAGGCAC[A/G]AGAATTGCTTGAACC | 11124 |
rs141056383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50526146 | ACTCCTGTTTTGACC[C/T]GTAGGTTAGCTTTCA | 11124 |
rs141063867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50876527 | TACGACAAACGAATA[C/T]GTCAAAGGGATATAA | 11124 |
rs141076383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50868521 | TTTAATCCCTTCTTC[C/T]CTTCTAATGTAAGCA | 11124 |
rs141088776 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50652101 | GGGCAGGCACCACTT[C/T]ACAGGTTCTGGGACA | 11124 |
rs141097284 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545678 | ACAGGAAAACCAGGA[A/G]AAAGTCACTACTATA | 11124 |
rs141112837 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50455075 | TACAGCAGGCAGACT[C/T]CGTTGGTGATACCAT | 11124 |
rs141126618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467063 | ACCCACTGCATGAAC[A/T]GCAGTATGAGGACTG | 11124 |
rs141133874 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | FAF1 | GRCh38.p7 | 1:50574807 | GTAGCTTTTTAATAC[C/T]ATCAAATATTGTCTG | 11124 |
rs141135568 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50712322 | AGTTTTGTTTTGTGA[C/T]GACTCTGAGGAGAGG | 11124 |
rs141140231 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50725708 | TGATCCACCCTCCTC[C/T]GCCTCCTAAAGTGCT | 11124 |
rs141143673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816823 | TTTGGGGTCTTACAT[C/T]TAATTCTTTCATCCA | 11124 |
rs141151645 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50607823 | TCAGCTAGTTCCTAA[G/T]GGGAGACCCAGAATC | 11124 |
rs141166978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949971 | AGCTAGGACTACAAG[A/C]ACATGCTATCACACC | 11124 |
rs141198842 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50905699 | TGAGAAGTGTCTGTT[A/C]ATATCCTTCACCCAC | 11124 |
rs141213271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50530928 | GGAAAGGAAAAGGAA[C/T]GCACTGCTGAAAACA | 11124 |
rs141225922 | in-del | -/A | 0.156319 | 0.231784 | intron-variant | FAF1 | GRCh38.p7 | 1:50496045 | TTAACCAAAAAAAAA[-/A]GAAATTTAGATGTAA | 11124 |
rs141233424 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50909750 | TAAGGTCTTCTCTAC[A/G]CTGTTTATTCTGGTT | 11124 |
rs141262610 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50528464 | TCAAAAAATGTTCTA[A/C]GAAACACTGACACTA | 11124 |
rs141264260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50900564 | AATTCACAAACTTTA[C/T]AAGCCAGAGCAAGTT | 11124 |
rs141272453 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50761291 | CCATTCCTTCTGAAA[C/T]TATTCCAATCAATAG | 11124 |
rs141275142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50577800 | CTGATCAGTACATTA[A/T]CAGAAGTCAATACTT | 11124 |
rs141275574 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50859543 | ATACCTAGGAATGTG[G/T]TTAACCAAGGAGATG | 11124 |
rs141277202 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50526428 | TAGCGAGACCCCATC[C/T]CTATTAAAAATAATA | 11124 |
rs141277326 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50661362 | TAAAATTTTTTGAAA[C/T]CTGGCCCACGATTCT | 11124 |
rs141282082 | snp | C/T | 0.118933 | 0.212888 | intron-variant | FAF1 | GRCh38.p7 | 1:50713472 | AGAGACGGTGTTTCA[C/T]TATGTTGGCCAGGCT | 11124 |
rs141282493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50777500 | GCATTTCATTATTAT[A/G]TATTTCCTAAGTCAA | 11124 |
rs141283739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50624093 | CCACTAGAAAGACCA[C/T]GTAGTTCCGTGGCAG | 11124 |
rs141298640 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739734 | CCTGAGAGGTTAGGT[A/G]ACTTGGATGAGGTCT | 11124 |
rs141308678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50854252 | CAGATTAGAATTTAT[A/G]ATGTTCATGTAGCAC | 11124 |
rs141312853 | in-del | -/CTTA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694448 | AAAAAAATCAGGAAT[-/CTTA]CTAATTATCTCACTT | 11124 |
rs141313368 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50841460 | CTTTGTGTTTCCATA[A/T]AGTTTTAAATTTTTC | 11124 |
rs141314967 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50758465 | TTATTGTTGTCATAC[C/T]TGTACTTGTACACAT | 11124 |
rs141320764 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50653396 | TTGCTCTTATTGCCC[A/G]GTGGAGTGCAATGGC | 11124 |
rs141324959 | in-del | -/AAACCC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50669009 | AAGGACATTAAAAAA[-/AAACCC]CCGCCACAAACCATG | 11124 |
rs141328556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470662 | TTTATGTGCTATGAA[C/T]ATAGTAATTTATATT | 11124 |
rs141333971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749311 | CTTGAAAACACTCTG[A/T]GCCCTCATGACTTAA | 11124 |
rs141354739 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50691906 | ATGTATACACTATGA[A/C]ATGATTAAATTAAGC | 11124 |
rs141362147 | in-del | -/C | 0.245916 | 0.249967 | intron-variant | FAF1 | GRCh38.p7 | 1:50847374 | CAGACAATACCTAAG[-/C]CAGATGGGTAATTAC | 11124 |
rs141384042 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50809146 | AGAAAAGTTTATAGC[A/G]CTGAACACCCACAGC | 11124 |
rs141384473 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50954188 | TCCTGACCTCGTGAT[C/G]CACCTGCCTCAGCCT | 11124 |
rs141411542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709049 | GAGTAATGGAAAGAC[A/T]TCCTGAGGTTTGAAG | 11124 |
rs141433417 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50945107 | CCAGATGCCTATGAA[C/T]GGCAGGGAGCATGGA | 11124 |
rs141443183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50705149 | CACCCTCCATGAAGA[C/T]AGAATTACTAGCTTT | 11124 |
rs141449415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616464 | CTGATTCTTCCAATG[A/C]ATGACTATGAATTGT | 11124 |
rs141456152 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50847483 | CTCATCAGTAGAACT[G/T]ACACAGTCAAGGAAA | 11124 |
rs141463702 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50959294 | GACCTCAGTACCCCA[C/T]TGTCATTGCCCTCGC | 11124 |
rs141472697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50594292 | TGCACTCCAGCCTGG[G/T]TGACAGAGTGAGATC | 11124 |
rs141480352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842441 | AAGCATATATTTTAA[A/T]ACTACATGCATTACT | 11124 |
rs141497835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461021 | TACCGAGTGGTTGAT[A/G]AAAATGTGACGAGAG | 11124 |
rs141502540 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50901048 | TAAAAAAAGTAGATA[G/T]AAAAATATGGAAGTA | 11124 |
rs141509272 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50775568 | CTAAAGCAAGAAAAG[A/G]TTTATCAAACAGAAT | 11124 |
rs141513680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50810241 | GCCTGGGCAACAAGA[A/G]CGAGACTCTGTCTCA | 11124 |
rs141517606 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50687932 | CAAGGTCAGGAGTTC[A/G]AGACCATCTTGGCTA | 11124 |
rs141519506 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50638735 | AGGCATGAGCCACCA[C/T]GCCCAGCCTAGCTAT | 11124 |
rs141528230 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50602276 | TCTCAAGCTTGTCAT[C/T]GTCCTCACAAGACAC | 11124 |
rs141536229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50945253 | TAGGGTCACGATGGC[A/G]TGGCCAGAGCCAGCT | 11124 |
rs141547741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50646781 | TTGCAACTTTAAGGG[A/C]CAGCACAGTTACTGG | 11124 |
rs141549228 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50614416 | TAGAGTTAAGGGGGG[-/A]AAAAAAAAGAATGTT | 11124 |
rs141553823 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50596626 | TTTAAAATTTCCATA[A/C]GATACATATATCAGA | 11124 |
rs141558135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50622348 | GCACCAGCATTCAGA[C/T]ACTCCACACAAGGTT | 11124 |
rs141559282 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50539253 | TACTTCTTCCAATTA[A/T]TCAACATTATAACAA | 11124 |
rs141573398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50770668 | ATATTATGAAAATGG[C/T]CATACTGCCCAGAGC | 11124 |
rs141582064 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50887793 | TAGCTTTGCAGTATA[C/G]TTTCAAGTCAGGTAA | 11124 |
rs141594276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50668399 | CTGGTCAGGTTATCT[C/G]AGTCTAACTTGCTAC | 11124 |
rs141602291 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50551826 | GAGAGTAGTCTCAAA[C/T]AGTTTACTAGCTGGC | 11124 |
rs141610232 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50510958 | CCTATGTATTATATA[C/T]ATTCTTTTATATGGA | 11124 |
rs141617535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50764269 | TACTAACTGTACCCT[A/G]TGTGCGACAAAGTCT | 11124 |
rs141634088 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50562923 | ATTCAGAAAAAAATT[A/G]TGTCTATACTGAACA | 11124 |
rs141637578 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460531 | GCTATGAATTCAATG[C/T]TAATGAACCAACAGT | 11124 |
rs141643976 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50910085 | GTCCTTTCTGTTTGT[C/T]AGTTTTCCTTCTAAC | 11124 |
rs141650642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50820719 | TGACACTTTTAGGTT[C/T]TACATGTAAGTGAGG | 11124 |
rs141656414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928501 | AAAAACTGAGGAAGG[C/T]GGCCAGGCGCAGTGG | 11124 |
rs141665862 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50643877 | GGATTACAGACAAGA[A/G]CCATCGCTGCCCCCA | 11124 |
rs141694380 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622185 | AAAAAAAATAAAAAG[-/A]AAAAAAAAAGAAAGA | 11124 |
rs141696261 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | FAF1 | GRCh38.p7 | 1:50600202 | ATCATGAGCTTGACA[A/G]CTTCTCAATGCTTAA | 11124 |
rs141700951 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50632870 | ACCTCCTCTATGATC[C/T]TTCCAGGTAAAATTC | 11124 |
rs141708243 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50515789 | TCAGCCTTCTCCCTC[C/T]TCACTTCTGTCTATA | 11124 |
rs141711349 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50910564 | GGGCCACTTTGTTTA[A/C]CTACTCAAGCCTCAG | 11124 |
rs141713281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50957153 | GTGTGTAGTTTTCCA[A/C]ATAATTTTTTCTTCT | 11124 |
rs141734097 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50916281 | TCCCATCTTCTAGAT[A/G]AGGAAATGACACAGG | 11124 |
rs141734153 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50869140 | TTCTTTTATCTTTGG[C/T]AATATGCCTTGTACT | 11124 |
rs141734869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50571575 | AATGGCCATGAAAAT[C/G]TATTAAAGATTAAGC | 11124 |
rs141743801 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50479717 | AATAAACAACAGTAG[C/T]TCGTTACTTCATTCA | 11124 |
rs141744516 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50768600 | CACTACTGAACCAGT[G/T]CAATAAAAATAGAAA | 11124 |
rs141757343 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50581022 | TCAAGTGATCCACTC[A/G]CCGTGGCTTCCCAAA | 11124 |
rs141758459 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50826910 | CGCCTCTGCCCAGCC[A/G]CCCCGTCTGGGAAGT | 11124 |
rs141763266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50491283 | ACTTGTGTTCTTTAC[C/T]TAATCAACTCTACCA | 11124 |
rs141763666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694434 | ATTGAGTTTTCATTA[A/C]AAAAATCAGGAATCT | 11124 |
rs141780344 | snp | A/G | 0.111576 | 0.20818 | intron-variant | FAF1 | GRCh38.p7 | 1:50953664 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 11124 |
rs141783572 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50953968 | TTTTTTTTTTATTTG[A/G]GACGGAGTCTCCCTC | 11124 |
rs141788843 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50442245 | GTCTTCTGAATCTGC[A/G]AGTGAGAGAAGAAAC | 11124 |
rs141799745 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50912055 | AAAAAAAAAAGGCAG[A/G]GTATTTAGAGGACCT | 11124 |
rs141803724 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50825662 | AGAATACCTGAACAC[-/A]AAAAAAACCCGACAT | 11124 |
rs141811210 | in-del | -/TAA | 0.492386 | 0.0612297 | intron-variant | FAF1 | GRCh38.p7 | 1:50614519 | TTGATCAACACATAG[-/TAA]TAATATTAGAAATCT | 11124 |
rs141822097 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50641831 | GTTACCAGGCACATA[C/T]ACATTTAGGATCATT | 11124 |
rs141827084 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50700341 | TCTTCTCAAATCATT[-/T]GGAGTCGAACGCAGC | 11124 |
rs141828142 | snp | A/G | 0.120326 | 0.21374 | intron-variant | FAF1 | GRCh38.p7 | 1:50729650 | AATCTCAGGTGATCC[A/G]CCTGCGTTGGCCTCC | 11124 |
rs141843042 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638833 | TTTGCTTTTGCTTTG[-/A]AAAAAAACTTATTTT | 11124 |
rs141854245 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50826321 | TTTTGGAGGCTGAAG[C/T]GGGTGGATCACTTGA | 11124 |
rs141858543 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50913786 | GAACTGATGGATGAA[C/T]ATCCAAACAGCAGAA | 11124 |
rs141877006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50658931 | TACCAGTATATGGAT[A/G]AAGCACAAGTGATAA | 11124 |
rs141877201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576221 | TAAGTCTCAAAACAA[C/T]CTCTATAAAGTAAAT | 11124 |
rs141879506 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50541686 | ATCTGCCCATAAGTG[C/T]TATTAAGTACTAGTA | 11124 |
rs141879889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876156 | CCAGAGGACACAGTA[C/G]TTGAGCAGGCTTCGT | 11124 |
rs141885083 | in-del | -/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50500704 | AAAGACAATTGAAAA[-/T]GATATTGAGTGTGCC | 11124 |
rs141888552 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50452565 | CAAGGCCAATACCAC[A/G]GAAGCAGCCAGGACC | 11124 |
rs141893480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772555 | TCCTCTGCAGCAATA[C/T]GGATGGAGCTGGAGG | 11124 |
rs141897361 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50919273 | ATAAAAAACAGTAAC[C/G]GTTTTCATGCTGGAG | 11124 |
rs141904163 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50795579 | TTAAAGTATGTGGTA[C/T]AAATGCTTTATATCA | 11124 |
rs141908577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709961 | ACAGTTCAGAAACGA[C/T]GATGGGGGAATATTA | 11124 |
rs141930554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50802009 | TCAGTAACTTCATCT[C/T]ATAAACATTATTTCC | 11124 |
rs141935515 | snp | G/T | 0.112631 | 0.208878 | intron-variant | FAF1 | GRCh38.p7 | 1:50759200 | ACATGTGCACAATGT[G/T]CAGGTTAGTTACATA | 11124 |
rs141938611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50857739 | AATTAAATTATCTAA[A/G]TATTCATAATAACTT | 11124 |
rs141957225 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50660271 | CAGATTAGCCTCAAA[C/T]GAGTTGTTCTAAACT | 11124 |
rs141960327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50576976 | CCAGCCTAAAAACAG[A/G]TTTTAAATGTCAGCT | 11124 |
rs141961380 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50665188 | TTTTAGGAATTTTAC[G/T]TTAACCTAACACCAT | 11124 |
rs141971714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50615167 | CGTGCATTACTTAGC[C/T]TAGGTAATGGCCTCC | 11124 |
rs141973734 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50531433 | AAACAGTGCATATAA[A/T]AAAATCAATCCATTT | 11124 |
rs141978084 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769045 | CTACTAAGTAGACTT[-/A]AAAAAAAAAACAGGA | 11124 |
rs141990488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582183 | ATTTGCGTAACTGAA[A/G]AGAATACAAATATGT | 11124 |
rs141991203 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50796952 | CTGAGCAACATGGCT[G/T]GGGCGAAACTCCATC | 11124 |
rs142003776 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50924699 | ATAATAAAAGATACA[C/T]AGGCTAGGCACAGTG | 11124 |
rs142013391 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50838443 | AAATATAATTTTACA[G/T]GTTAATGTAAAATTG | 11124 |
rs142017278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50716442 | ATTAATTCATACTGA[A/G]AGGTGAAGCCAGCTG | 11124 |
rs142021037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50533641 | ATTTGCAATACCTAA[A/G]GGATAGTCTATTAAA | 11124 |
rs142029735 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50597280 | CACCTAGACTGTTCC[A/G]TGAGAGAAGCCCACT | 11124 |
rs142032718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50509568 | AGTGAGCTGTGACTG[C/T]ACCACTGCATTCTAG | 11124 |
rs142034779 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50936238 | AGAACTCACAAATTA[G/T]TAAGAAAGACAAACA | 11124 |
rs142050721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50483601 | TGAAGTGACATGATG[G/T]GACAAATGATTTTTA | 11124 |
rs142075777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949358 | CCAGAAAATTCTTTA[A/C]TATCGGGCGATGCCT | 11124 |
rs142077187 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50662647 | TTATTTAAAGTAACA[A/G]CTAATAATCACACAT | 11124 |
rs142082131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50581864 | AGGCAGGGAATGGGA[A/G]GAGCTGAAGCTACAT | 11124 |
rs142093012 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50660708 | CATGTTGGCCAGGCT[A/G]GTCTCGAGCTCCTGA | 11124 |
rs142099909 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50543485 | GTATAAAGTGGAAAT[A/T]ACACTTACCTTTAAA | 11124 |
rs142105761 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50844962 | AATAAAGGTTTAATA[A/C]AATAAAAGGTACAGA | 11124 |
rs142113363 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50922185 | AAAAAAAGGCCAGGC[A/G]CAGTGGCTCACACCT | 11124 |
rs142115437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50797745 | GCAAGGTGTCACGTG[C/T]CTGTAGACCCAGTTA | 11124 |
rs142115646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930575 | GCACAGTGGCTCAAG[C/T]CTGTAATCCCAGCAC | 11124 |
rs142116855 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50619116 | ATCCCTTTACTTTGA[C/G]ACTGTGGGTGTCATT | 11124 |
rs142132591 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50592912 | CACTGTACTTCAGCC[C/T]GGGCAACAGAGCAAG | 11124 |
rs142142028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943541 | ACCTTAATGCCTTCC[A/C]GGGCCAAGGTGTTGT | 11124 |
rs142150192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50859159 | CTCACACCTAATATA[C/T]TGAATGGCCAAAAAC | 11124 |
rs142156956 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50515518 | TATGCTCAAAGACCA[C/T]AGTTTGAAAAGCACG | 11124 |
rs142165669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645530 | TGGCACAGTACATTA[A/G]GAAATCAATGTGGCC | 11124 |
rs142196683 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464497 | ACTGCATTTTACTAA[A/G]GGGAATGCAATAAAC | 11124 |
rs142201244 | in-del | -/TATGTGTG/TGTGTG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637681 | TCACACATATATATA[-/TATGTGTG/TGTGTG]TGTGTGTGTGTGTGT | 11124 |
rs142207006 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50710759 | AGGTGTGTGCCACCA[C/T]GCCCGGCTAATTTTT | 11124 |
rs142208166 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50927533 | GCGGCAGAGTGAGAC[A/C]CTGTCTCCAAAAAAA | 11124 |
rs142215938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933084 | TCCTGGGCCTCCGTG[C/T]CTATGATGAGAGGGG | 11124 |
rs142225020 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50748543 | ACTGAAAGGTAAAAA[A/C]GCAAAAATAGACATG | 11124 |
rs142226558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50807234 | AACAATTTTAAAACA[C/T]GGTCACAGGTGTATT | 11124 |
rs142235669 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50661784 | AAAGGCTTATAGTTA[A/C]GAAAGCAGTCACTTC | 11124 |
rs142246777 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50850071 | AGGGATAAAACTTCG[G/T]GTCAGCTTTAAAGGA | 11124 |
rs142257992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50934788 | TGAAGGATAATTTTG[C/T]TGAATATAAAATTCT | 11124 |
rs142261589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50690859 | TTTGTGTTTAGTTTC[C/T]TTCATTTAGCATGTT | 11124 |
rs142272863 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50609613 | TCTCGAACTCCTGGG[C/T]TCAAGCAATCCTCCT | 11124 |
rs142277197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488455 | AGCCAGTATGGTTGA[C/T]GATACACTAATACAC | 11124 |
rs142280332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952099 | GCCCTCTCCCTCTCC[C/T]CTTTCTACGGTCTCC | 11124 |
rs142280723 | in-del | -/TA | | | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462070 | AACATATCAATATTT[-/TA]TATATATATATACAC | 11124 |
rs142290785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50799251 | ATGCTTGTGAACTTG[A/G]GCAAGTCTATGTAAA | 11124 |
rs142290898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50744275 | CCTATTATCTTTGTT[C/T]CATAATCAATACTTG | 11124 |
rs142291088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50875173 | TGTTACAAAAGTAAT[A/G]GTTTCCAGCTGTCCC | 11124 |
rs142298884 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FAF1 | GRCh38.p7 | 1:50892423 | GCAGAAATCACCCAT[C/T]TTCTGTGTCGCTCAC | 11124 |
rs142299114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50833245 | ATCTTGGCTACAAAT[C/T]TGAAGTCTCCACAAC | 11124 |
rs142308228 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50796213 | GCAGCAAACACACAA[-/AC]ACACACACACACACC | 11124 |
rs142318499 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503036 | TAGAGATGGGGTCTC[G/T]CTATGTTGTTCAGGC | 11124 |
rs142319609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50556475 | ATGCTAAAAACTCAG[A/G]TTTCACCACTATACA | 11124 |
rs142329553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50824880 | GTTCTCATTCATATG[C/T]CAGAGCTAAAAAAAA | 11124 |
rs142348409 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | FAF1 | GRCh38.p7 | 1:50636635 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 11124 |
rs142348468 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50686493 | GTTGCCGTGAGCTGA[A/G]ATTGCACCATTGCGC | 11124 |
rs142350045 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50681526 | TCTTTTCTTTTTTTG[A/C]GACAGAGTTTCACTC | 11124 |
rs142350461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551002 | AATGATTATATGCCT[A/G]TGACATGTCCTTTCT | 11124 |
rs142358101 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50598709 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 11124 |
rs142369986 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50560408 | CATTAAGTTCAAAAG[C/T]TAATACTGACAGGCA | 11124 |
rs142373908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468927 | AAAATTTAAAACTTA[C/T]AATTTAGAAAATAAA | 11124 |
rs142398600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614224 | TCCCAAGACAAGCAT[A/G]TATTCTATGGGCAGA | 11124 |
rs142419834 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50780368 | GGTTTTAGTCCATCA[A/C/T]CAAGTTTGACCTGGC | 11124 |
rs142423844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50882662 | AATGTGTATGTATGT[A/G]TGTATGTGTAAACAC | 11124 |
rs142425135 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50747140 | CACACACAGTCTCCA[C/T]TGGGGCACTGCCTGG | 11124 |
rs142425517 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50552206 | GGAGGTTGAGGCAGG[A/G]GAATAGCTTGAACCC | 11124 |
rs142442783 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461621 | GTAAAAAATCTCTAT[A/G]AGGAAATACGCCTGT | 11124 |
rs142484923 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50639270 | AAATTCAAGTACAAA[A/T]CTTTGTGAGAACATG | 11124 |
rs142493892 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50685000 | AAGGCTAACTCAGGA[A/G]ATAAGGAGAGGTTAT | 11124 |
rs142526830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872559 | AGCAGTAGGGTTTGA[A/G]AGGATTGACTCCAAT | 11124 |
rs142542757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619067 | TGGCCCCTTGCTCTA[C/T]TATGTTTTATTTCTG | 11124 |
rs142546171 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50771070 | AAGACTGAAACTGGA[C/T]CCCTTCCTTACAGCA | 11124 |
rs142565479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50751877 | TCTCTCTCTTTTTTG[C/T]GAAGGACTGGTAATA | 11124 |
rs142569050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50489526 | TTAGGCATACCTCTA[C/T]AATAACGTTTACATA | 11124 |
rs142577879 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50537561 | TTAAAATAGAAATAT[G/T]TAAAATAAATTTATC | 11124 |
rs142581750 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50445764 | GGCTTGATTTTGTCT[A/G]TAGTTAGAAAAGGAA | 11124 |
rs142594028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50767407 | TAGGATATAATTCGC[A/G]AAAATTTCCCCAGCC | 11124 |
rs142594967 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50914214 | ACCTGGTATTAACAG[A/C]TATGATTTAATTTTA | 11124 |
rs142596754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50812784 | TGTATCTGTTCATCA[C/T]AGCACTATTCACCAT | 11124 |
rs142612011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50683924 | GCGACAAGGGCAACA[C/T]TCCATCAAAAAAAAA | 11124 |
rs142613634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50685886 | TCAAATTACTATGAA[A/G]TAAAAACCATTCTCC | 11124 |
rs142635926 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50946834 | AATACAGAAGAGGAA[C/T]TCACAGCCTAAAGAA | 11124 |
rs142643907 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50623424 | ATACAAAGAAATTAG[A/C]TGGGTGTGGCGGCGT | 11124 |
rs142653735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823476 | TACCTCATTAAATAG[A/C]AATTCCATTCTTCCA | 11124 |
rs142660488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50506358 | GCTTGACCCAAACAA[A/G]CCCTCTCACAATTCT | 11124 |
rs142667967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50878693 | ATACCACAAGATAGA[C/T]ATTATTATGCCCATT | 11124 |
rs142692821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757578 | ATCCTTCAGGTTATG[A/G]TTACAATTTTCATAC | 11124 |
rs142724402 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50639024 | ACTGACTGGATTTCT[C/G]TAAGTTATAGCTTTG | 11124 |
rs142724701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50554644 | AAATCACTCTGATCA[A/G]ATTATTACAAACTGG | 11124 |
rs142729050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50763604 | TTCCCTCTCCAGCCT[A/C]TAGCTCCCAGTATTT | 11124 |
rs142729164 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50716766 | TGTAAATGCACCAAT[C/T]GGCACTCTGTAAAAT | 11124 |
rs142753919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50858352 | TCAACCCATACCATG[C/T]ACTTTATATAAAAAC | 11124 |
rs142760654 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50617197 | TAGGAGTGGTGAGAG[G/T]AGGCATCCTTGTATT | 11124 |
rs142767925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50868475 | TAAGTTGCTCTTCCA[C/G]CTTCTTACGGTGGAA | 11124 |
rs142774985 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724256 | AAAAAAAAAAAAAAA[-/C]AACCATATATATATA | 11124 |
rs142792770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50651941 | AGTTATAAGCCATTT[C/T]TGGCTAAATTCAAGC | 11124 |
rs142803842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50695027 | ATAGAAGGAAAGAGG[C/G]TAAGAAAGTCAATGT | 11124 |
rs142807959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50612132 | TTATTAGAAATGTAA[C/T]ATTTTCTGAAGATAT | 11124 |
rs142815390 | in-del | -/GC | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460834 | TGTGTGTGTGTGTGT[-/GC]AGAGAAAGGGTCTCA | 11124 |
rs142821928 | snp | C/T | 0.000115427 | 0.00759606 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788076 | GTCCAGCATCCGAGG[C/T]TGCCTTTCTACAATC | 11124 |
rs142871704 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50570406 | TTTGTGGTAAGCGAC[C/T]GGCTCGCCTCGCCCC | 11124 |
rs142887474 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50519156 | CCAGCATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 11124 |
rs142888945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621596 | ATAGAGACAGGGTTT[C/T]ACCATGTTGCCCTGG | 11124 |
rs142926112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940970 | AATTTTAAAAATCAC[A/C]TTTAAAGAATAAAGA | 11124 |
rs142926350 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50891195 | GTAGTTCTTGTGCCA[A/C]GGTTTTCAGTTCCAT | 11124 |
rs142931721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916309 | AGGATTAAGTAAATT[A/C]TTCAGTCACACAGCT | 11124 |
rs142937833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50564114 | CACAGTATACTGTGA[C/T]TGAAGAACTAATGCC | 11124 |
rs142938304 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50828859 | AAGACTCATTAAAAG[A/G]GCAAAAACACAAGCC | 11124 |
rs142938491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50797116 | ACTTCAGCCTGGGTG[A/G]CAGAGTGAGACCTCA | 11124 |
rs142939416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50615958 | GAAGGGTATTTCCCA[C/T]GTTTTCTTCTGGGAT | 11124 |
rs142939668 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50473054 | TCTGGAACCAGAGAT[A/T]AGGGGAGCCTGAGGT | 11124 |
rs142949003 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50455846 | AATTTTGGGGGCCAG[A/G]TGCATCACTTGAGGT | 11124 |
rs142963905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50557189 | TATTTGCTGAAAAGG[A/C]CTTTCTTGGTGCTGA | 11124 |
rs142966979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923732 | AAAAGATCACTCACC[A/G]TAAGTGGGATTTATG | 11124 |
rs142975619 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50878829 | TATGACCATTTTAAC[-/A]ATGAGATTAAGCAAT | 11124 |
rs142979585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466303 | AACAAAAAGAATGAA[A/G]CTGCCATTTAATCAG | 11124 |
rs142989390 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50935055 | TCTTAAATCTGTATA[C/T]TTATGTCTCACACCA | 11124 |
rs143005323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870022 | TGTTTCCTGTACATG[C/T]ATTTGCTGAACTTTA | 11124 |
rs143011339 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50769910 | ACAAAAATTAGCTGC[A/G]CGTGGTGGCCCATGC | 11124 |
rs143013445 | in-del | -/A | 0.14665 | 0.227637 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466042 | GTGATTTGCCTTATT[-/A]AAAAAAAATCGCTGT | 11124 |
rs143013782 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50663400 | AGCATTGCTTTTTTT[A/T]AAATTTTAATTTCAA | 11124 |
rs143019991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652716 | ATCTAAATTAGCTCT[A/G]TCCTCACTCACTCTG | 11124 |
rs143026851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50536726 | ATTACTTACAAGCTA[A/T]ATAATCTAGTACCTG | 11124 |
rs143036478 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50920173 | GGGTGTGGTGGCACT[C/T]GCCTGTAGTCCCAGC | 11124 |
rs143037429 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50913499 | AGAGACCTTGCAGAT[A/T]TCTTCAAGATGTTAA | 11124 |
rs143053121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50702527 | ACAGAAAAGATTTTT[C/T]GTCTTTAAGACTACT | 11124 |
rs143067155 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50790647 | AGAGAGAACCATAGG[A/T]GTGTTTCAGTTGTAA | 11124 |
rs143068569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50894877 | TTACAGCAAAAGCAA[A/G]AGGGAAGTACCAAAT | 11124 |
rs143082507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50802911 | AAGTATTTGCCACAG[C/T]TTTGTCAAATTCACA | 11124 |
rs143113861 | snp | A/C/G | 0.00016489 | 0.00907852 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788074 | AAGTCCAGCATCCGA[A/C/G]GTTGCCTTTCTACAA | 11124 |
rs143114469 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50888724 | GAAGCCCACCTGATC[A/G]TGGTGGATAAGCTTT | 11124 |
rs143119473 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | FAF1 | GRCh38.p7 | 1:50884511 | TGGGCCACAGAGTGA[C/G]ACTCTGTCTCAAAAA | 11124 |
rs143123212 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50576087 | AGAACTAGTTCATAA[C/T]TGAATGAGAAAATCA | 11124 |
rs143156511 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50709912 | ATGGACAATAATTTG[A/G]TAAGTAGATATGGAG | 11124 |
rs143167159 | in-del | -/AAGG | 0.499993 | 0.00188599 | intron-variant | FAF1 | GRCh38.p7 | 1:50490492 | GGAAGGAAGGAAGGA[-/AAGG]AAGGAAGGAAGGAAG | 11124 |
rs143168205 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50501784 | TTTGGAAAACACTTC[A/G]GCAGTTTGTTAGAAA | 11124 |
rs143181568 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50840496 | TAAGAACACAGGAAG[A/G]TTTATAAGGAATCTT | 11124 |
rs143202373 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50632147 | ACAATAAGAAGTAAG[A/G]GGTACGATGAACACT | 11124 |
rs143218158 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50938758 | TAATTCTCATATATG[A/C/G]TGAAAGGTAAGGGTC | 11124 |
rs143235822 | in-del | -/AC | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50903139 | TATCCCCAGTGCACA[-/AC]ACAGATACCTGTTCA | 11124 |
rs143235929 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922314 | AAATACAAAAATTAG[C/T]TGAGCGTGGTGGCAG | 11124 |
rs143255468 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50861288 | GAATATCTGTATCCT[C/T]CTATGGTGACATCCT | 11124 |
rs143258533 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50835635 | TCCAAATCTCTATTA[C/T]GAAACTGTAAAATTG | 11124 |
rs143270508 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50743475 | TTGGATTACAGGGGC[G/T]TGCCACCACGCCCAG | 11124 |
rs143275326 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50455356 | GTGACTTAGCTGCCA[C/T]CTGATCCTAAGCTCT | 11124 |
rs143286078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50592569 | AGGAAATATAACTAC[A/G]ATCCATAAAGTCTAA | 11124 |
rs143286402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50801931 | TAAAGTCTAGTTCCA[C/T]AGTTCTGATTCAGGC | 11124 |
rs143288586 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50892539 | CTGCAGCCTGTAAGG[A/T]TTCCACTGAAAACTC | 11124 |
rs143300836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50595242 | TATTTTTAGTAGAGA[C/T]GGAGTTTCTCCATGT | 11124 |
rs143300969 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50678989 | CTACTCGGGAGGCTG[A/C]AGCAGGAGAATGGCA | 11124 |
rs143302334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50503704 | ATACTATTCAGCAAG[C/T]AAAAGGAATGAATTA | 11124 |
rs143309703 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50505165 | TTAATCCACACTGGG[A/G]GAGAAGAATGGTTAA | 11124 |
rs143311114 | in-del | -/G | 0.00283784 | 0.0375615 | intron-variant | FAF1 | GRCh38.p7 | 1:50441564 | AAAAGACTGAAACAA[-/G]CACTATATTCTCTAC | 11124 |
rs143318164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860889 | TGTATACACTGTGGA[A/C]TACTATGCAGCCATC | 11124 |
rs143324329 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50733346 | TGTCTCCAATCTTCT[A/G]TTATTACACCTTTCC | 11124 |
rs143327398 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637701 | GTGTGTGTGTGTGTG[-/GT]TGTGTGTGTGTGCGT | 11124 |
rs143329410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648045 | AGGTGGATAACCTGA[A/G]GTCAGGAGTTAGAGA | 11124 |
rs143345841 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50637088 | TTGTATTGAATATTA[C/T]AGTAATATTTTTTGA | 11124 |
rs143348139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588757 | GTCCTCTGCTGTGCC[G/T]CTGTGTCCAGCAACA | 11124 |
rs143353186 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50678236 | TGAACTTATGAAAGA[C/T]TGGAGAAATTCCTAT | 11124 |
rs143357209 | in-del | -/A | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50829101 | AATGGATTAAAAGCT[-/A]AAAAAGGCTGACAGG | 11124 |
rs143368457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50476340 | TTATTGGCAGAAGGA[C/G]ACCACAGTCCTAGTT | 11124 |
rs143374908 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460947 | TGTGAGCCACAGCAC[A/G]TGGCCTAAGTAAAGT | 11124 |
rs143382649 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50863072 | TATACATTCTATTCA[A/T]CAGTACATGGAACAT | 11124 |
rs143388511 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50809158 | AGCGCTGAACACCCA[C/T]AGCAAAAAGTTAGAA | 11124 |
rs143392135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945727 | TATCTTTAACTTGCC[A/C]GTCTATAGCTTTCCA | 11124 |
rs143405610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50601256 | TGCAAAGGAAAACTC[C/T]AGTAAACCATCATGA | 11124 |
rs143410987 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50907292 | TTTGCCAGTATTTTA[C/T]TGAGGATTTCTGCAT | 11124 |
rs143411199 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50475223 | GGAATAGGGAAAACA[A/G]CTAGGAAGGAAGATC | 11124 |
rs143414411 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50945151 | TTGACAATCAGTTCA[C/T]TGCTGAGTGGCTTGT | 11124 |
rs143419644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50820139 | GATGGGGTGGAGAGG[A/G]TAGGGAAGAGGGAAT | 11124 |
rs143427019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50818991 | ATTTTTGGCTTCATT[C/T]AGACTGTGACCCATC | 11124 |
rs143432183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50472602 | GTATTGTTTTGGTTG[A/G]GGGCGGGTGGCAGGC | 11124 |
rs143433357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50634144 | AAAGGCTACTTACCA[C/T]GCATAAATGTTCATT | 11124 |
rs143436728 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50693962 | TATTTCTGATATTTC[A/T]AATTTCAAGCAAAGT | 11124 |
rs143437699 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | FAF1 | GRCh38.p7 | 1:50611707 | ATCAATGCTAATGTT[C/T]ACTAGGAAAACAGGA | 11124 |
rs143443661 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50549354 | CACTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGC | 11124 |
rs143446041 | snp | C/G | 0.111576 | 0.20818 | intron-variant | FAF1 | GRCh38.p7 | 1:50953366 | CAAATCCCCCTCTCC[C/G]AGAAACACCCAAGAA | 11124 |
rs143452712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50942625 | CCACCCTACTTACTG[A/G]CAAGCTAACAACCTG | 11124 |
rs143456410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452545 | AGGGGACATGCCTCA[C/T]TTTCCAAGGCCAATA | 11124 |
rs143462519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836165 | TGTTTTTGTTTTTTG[C/T]TTCTGTTTTTTTTTT | 11124 |
rs143469087 | snp | C/T | 3.35897e-05 | 0.00409802 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50705789 | GACATAACTCACCTC[C/T]TGAATAGTACTGCTT | 11124 |
rs143469783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744109 | TTATATCTGAGGTTG[C/T]TACTGGGTTCCTAAG | 11124 |
rs143505387 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50765359 | TTAACCAATACATTA[C/T]CTACAGAATTTAATA | 11124 |
rs143507189 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50629143 | CAAAAAGATCAATCT[C/T]ATAGATCCAGATAGA | 11124 |
rs143509944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50562415 | CCTCAATTATTTCAA[C/T]CACTGACCCTTTGTT | 11124 |
rs143510256 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50545872 | GAATACTGGGTGTAA[C/T]CCATCAATTACTGGA | 11124 |
rs143512046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471649 | AGATCTAGAAAAAGG[C/T]ACGTTCCCTAGGCTA | 11124 |
rs143529806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50811144 | GTTCAAGACCAGTGT[A/G]AGCAACATGGCATAA | 11124 |
rs143537598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616337 | TCTTTCTAGGTTCCA[C/T]ATTAATTTTAGAATT | 11124 |
rs143538129 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50721915 | AGTAGGAAGCCACTG[G/T]GCCTGGCCAGGTCTC | 11124 |
rs143566728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749322 | TCTGAGCCCTCATGA[C/T]TTAAAAGAAGTTTCT | 11124 |
rs143576568 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662517 | TTTTGGCCATCCTGA[A/G]ACACTACCCAGCATA | 11124 |
rs143586777 | snp | A/C | 0.031825 | 0.122064 | intron-variant | FAF1 | GRCh38.p7 | 1:50540498 | AGTAGTAGGTCTTCT[A/C]GTTTCATACTTAGCA | 11124 |
rs143593425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50523358 | TGTTTTCCATAGCAG[C/T]TGCCATTTTACATCC | 11124 |
rs143618220 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | FAF1 | GRCh38.p7 | 1:50654000 | TATTTTCTGATTATT[A/C]AAGTTTCTGATTTTT | 11124 |
rs143624277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50740380 | TCCTTCCTGGGGAGG[A/G]GCAATCTTACACAAG | 11124 |
rs143673931 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FAF1 | GRCh38.p7 | 1:50887277 | GGTTCTGGATATTAG[C/T]CCTTTGTCAGATGAG | 11124 |
rs143683037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50859885 | AAACAGCATGGAATC[A/G]ATACAAAAACAGACA | 11124 |
rs143689674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591712 | CTTTTACTGCTTTCT[A/G]CAGTTCCAAATTCTC | 11124 |
rs143692642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502949 | CCTGCCTCAGCCTCT[A/G]AGGAGCTTGGATTAC | 11124 |
rs143703999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50611784 | ACCCACCGTACATTA[C/T]TTGGTCAGAGTTAAC | 11124 |
rs143706149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50527683 | GTAGTTTCATCCAAC[C/T]GTAAAGTATCTCTCT | 11124 |
rs143708047 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50848273 | TTATGTTCCTGGCAT[A/G]TGCAAAAGTAAATTG | 11124 |
rs143713416 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50754428 | GGTTTTCCAATCTAG[C/G]TGGTAGGAACAGACA | 11124 |
rs143716502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50635865 | CAGCTACTAGGGGAA[C/T]AGACTAAATACTTTG | 11124 |
rs143742737 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50528705 | AGTCCACTTACATGG[A/C]GAGTTTTTTCAATAG | 11124 |
rs143744520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772732 | GAGGGTGAAGATCAA[A/T]AAAACTACCTATCAG | 11124 |
rs143759148 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50657590 | CAAAAACTTCAATAG[C/G]GTTCTTCATACTTCA | 11124 |
rs143767260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50608489 | GCCCAGGCCATAACC[A/G]TGTATGACATTTCTG | 11124 |
rs143771234 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50521238 | TCCCTCAGTTTAGTA[C/G]TAAACAAGGTAAAGG | 11124 |
rs143776439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50948846 | CTCTTAAACAATCAG[A/G]TCTCACGTGAACTAA | 11124 |
rs143778922 | in-del | -/T | 0.127254 | 0.217792 | intron-variant | FAF1 | GRCh38.p7 | 1:50571988 | CAATGTAGTTCATAG[-/T]TTTTTTTCAGTGTTA | 11124 |
rs143795599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50508378 | ACAAAATGTGGTATA[A/T]CCATACAATGGAATA | 11124 |
rs143802123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50887470 | CCTATAGCCTGAATG[A/G]TATTGCCTACATTTT | 11124 |
rs143813643 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50758971 | CCTCAGCCTTCCGAG[G/T]AGCTGGGACTACAGG | 11124 |
rs143826399 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50839538 | AGAAAGGGCCTAAAT[A/G]CTGTTGATCAGATTT | 11124 |
rs143829015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50557100 | TTCTCAGATTTGAGG[C/T]ATGGCAATCAAGGCT | 11124 |
rs143830735 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50641836 | CAGGCACATACACAT[A/T]TAGGATCATTCTGTC | 11124 |
rs143852461 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50497838 | CAGGTGTGTGCCACC[A/G]CGCCCGGGCTCAAAA | 11124 |
rs143867195 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50573404 | GTGCCTGGCCTGAAG[C/T]GGAATTTTAAATATA | 11124 |
rs143872224 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961531 | TTGACTTGGGAAAAT[A/G]TCAGCTTCTGGATTG | 11124 |
rs143893800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689953 | ACTCTACAGTATACA[C/T]AGGAAGATCATTGTG | 11124 |
rs143906211 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50791831 | AAATTTCCTCTGCTG[A/G]AATATCTAGCATGTT | 11124 |
rs143914572 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50707038 | AAAACCCCGTCTCTA[C/T]TAAAAATGCAAAACA | 11124 |
rs143914634 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | FAF1 | GRCh38.p7 | 1:50652127 | GGACAAGGTGCAAAT[A/G]GCAATAATGAGGCTA | 11124 |
rs143917151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50832712 | TCTTTTCCCTGTCTT[C/T]ATGCTGTTTCTGACT | 11124 |
rs143917189 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50890263 | TGTGTGTCTCTGCAC[A/G]TGAGATGGGTTTCCT | 11124 |
rs143924020 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50935373 | TAGCATGTCAAGAAT[A/G]TAACATATATTTCCC | 11124 |
rs143925544 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50740775 | CCTGAAACTTTATGT[C/G]AAATATGTGATATCC | 11124 |
rs143928457 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50567366 | TAAGAGAGTACTTTA[C/T]ATTTTGGAGTTCCTA | 11124 |
rs143939267 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50916271 | AACTTATTATTCCCA[-/T]CTTCTAGATGAGGAA | 11124 |
rs143941771 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50852334 | ATATCCAAACAATAG[A/T]GAAAGAACAGACCTA | 11124 |
rs143947378 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642739 | ATCTTTTCCTTTTAA[A/T]GTAATTCATACTTAC | 11124 |
rs143953344 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50638617 | CCCAGCTAATTTTTT[C/T]GTATTTTTAGTAGAG | 11124 |
rs143959388 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50927379 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAGCCA | 11124 |
rs143993075 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50776107 | CTATGAAGAATATGA[C/T]TGGAAATATTTTAAA | 11124 |
rs143995695 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50454736 | TATACTTTGACCAGG[C/G]AAGAGATCCTAGAGG | 11124 |
rs144011555 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50689510 | AATGCCGTGGACCCG[C/G]GAGGCAGAGGTTGCA | 11124 |
rs144037382 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50815746 | ATAGCCATTCTGGCT[A/G]GGCACGGTGGCTCAT | 11124 |
rs144037545 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50886445 | CAGGTTTCTTAGATA[C/T]GTACACATGTGCCAT | 11124 |
rs144037980 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50931019 | CATGATATATTGTTT[C/G]TCCATCCTTTTATTT | 11124 |
rs144044122 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460809 | CTAAGTATTTGTATA[-/TG]TGTGTGTGTGTGTGT | 11124 |
rs144048870 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50786379 | AATACTGCATTATTC[C/T]ACTTCTATGAGGTAT | 11124 |
rs144052430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50832526 | TTTAACATATATGAG[A/C]GTTTGACAAACACTA | 11124 |
rs144061409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549158 | CTGCTGCATAACTTC[G/T]AGAATATGCACCAAC | 11124 |
rs144070447 | snp | C/T | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50458166 | TGCAGTGAGCTGAGA[C/T]TGAGCCATTGCACTC | 11124 |
rs144072197 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50546850 | AGCAAGTCCCTTACA[A/T]GAAGAAAAACTGCAT | 11124 |
rs144074073 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50492997 | GTTAAACCTGATAAT[C/G]TCTACCCTTTCAGTC | 11124 |
rs144077009 | in-del | -/GT | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50588597 | ACAAGATACCAAGTG[-/GT]GTGTGTGTGTGTGGT | 11124 |
rs144079884 | in-del | -/A | 0.0729998 | 0.176553 | intron-variant | FAF1 | GRCh38.p7 | 1:50545637 | GTCAGATTAGTAAAG[-/A]AAAAAAAACTGGCTT | 11124 |
rs144090696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722988 | AAGTCAGAGCTCTCA[C/T]GGATGTGACTTATGT | 11124 |
rs144094834 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50635362 | ACTTTCCCTCTACAA[C/T]TTGAAATGCAAAGAA | 11124 |
rs144113547 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50866576 | ATCAAACCGAGAACT[C/T]AACCCCCTTTAAAAT | 11124 |
rs144126035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858965 | GTATACTTCATTCTT[A/G]GGATACAAGGTTGGT | 11124 |
rs144135319 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50679855 | AGTACAGTCTAAACC[A/G]CACATCTCGGCAACT | 11124 |
rs144141399 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50543058 | AGAATATCTGATGGT[C/T]AGCATGTATTAATCA | 11124 |
rs144156271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645060 | CTTTCAAAGCTGTTC[C/T]TTCCATCTGTTTAGT | 11124 |
rs144160318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559486 | TGAACAATTACTGAG[C/T]CCATTTTGAAACCCT | 11124 |
rs144163070 | snp | A/G/T | 0.0091479 | 0.0670627 | intron-variant | FAF1 | GRCh38.p7 | 1:50726468 | TTGGGTGGCCGAGGC[A/G/T]GACAGATCACGAGGT | 11124 |
rs144165484 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50591337 | AGAGCGCTCTTCACT[A/C]AACTGTGTATTTGTG | 11124 |
rs144167825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852422 | TCACAGACAAAATTA[A/G]TAAGAAACACAATTC | 11124 |
rs144181036 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50613797 | TTTATATTAAAAAAA[-/A]CAAACAAACAAAAAA | 11124 |
rs144186467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50708469 | GAGAGTGAAGTTTTC[A/G]TTCAAAGTTTGAGAT | 11124 |
rs144188309 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50757033 | CTATGGTTTATTTAG[A/C/G]AATATGTTGTTTAAT | 11124 |
rs144193502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50907080 | GTTTATTGAGAGTTT[C/T]TAGCATGAAGGGCTA | 11124 |
rs144199775 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50740791 | AAATATGTGATATCC[C/T]TTTGAAATTGATGAG | 11124 |
rs144208374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50474582 | CTGGTTGGGATTACA[C/T]CTCTAAAACAGGAGC | 11124 |
rs144224236 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50538015 | ATCTTTTATCTATAC[A/C]TGATTTTATAACATA | 11124 |
rs144232598 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50846742 | TGATTAGACCGAATA[C/T]TGTCAAACACCCTCT | 11124 |
rs144233127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50446538 | CTTCAGATAAGGGAT[A/G]CTCCACCTGTACTAT | 11124 |
rs144242929 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50791249 | TGAACAGAATCTGTG[A/C]GATGACATTTCACAT | 11124 |
rs144246325 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50887643 | ACAGGGAATCCTTTC[C/T]CCATTTCTTGTTTTT | 11124 |
rs144253020 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50752816 | GCCTCCAGTGTAGCT[G/T]GGACTACAGGTACAC | 11124 |
rs144253773 | in-del | -/GAAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519416 | AGGGAGGGAGGGAGA[-/GAAG]GAAGGAAGGAAGGAA | 11124 |
rs144257273 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50588086 | AAGGTCAGGAGTTCG[A/C]GACCAGCCTGGCCAA | 11124 |
rs144258697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50668157 | TAAAGTGGCCTGGGG[A/G]TGTGGCTCATCAAGT | 11124 |
rs144261202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50627443 | AAATGCCTGCCTCAT[C/T]AATAGTAGAACAGAT | 11124 |
rs144261228 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50577738 | TTTATAGCCCTCAAC[C/T]GGATGAGTGTCCTTC | 11124 |
rs144288794 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50905334 | CTATTGTGAATAGTG[C/T]CGCAATAAACATGTG | 11124 |
rs144288831 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50951191 | CTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 11124 |
rs144304254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50813017 | GTAGGAGGTAAATAC[A/T]CAGTTACATAGATAC | 11124 |
rs144325946 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50623365 | CTGAGCTCATGAGTT[C/G]GAAACCAGCCTGGGC | 11124 |
rs144330032 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50711661 | TAGTAGAGACAAGGT[C/T]TTACTATATTGGTCA | 11124 |
rs144332594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50453415 | AGTTTAGTCCCTAAC[A/G]ACATACAAAAGACTT | 11124 |
rs144345054 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50797385 | AGATTTACTAATCTA[C/T]AAATACCTTTTTTAA | 11124 |
rs144355976 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50711545 | CATGATCTTGGCTCA[C/T]TGCAACCTCCACCTC | 11124 |
rs144362412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50592845 | TGGGAGGCTAAGGCA[C/T]GAGAATTGCTTGAAC | 11124 |
rs144363552 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50892457 | GGGAGCTACAGACTA[C/G]AGCTGTTCCTATTTG | 11124 |
rs144382520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50929748 | TGGCTCCTGCCCCCA[C/T]GATTCACAATTATTC | 11124 |
rs144383412 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50742355 | AGTAAATTGAAGTAT[C/T]TGTAACCAAGGCTGT | 11124 |
rs144417351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50560063 | GCTGGAAATTAATAC[C/T]CCTGTGTCTCCCATG | 11124 |
rs144419281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468200 | TATGACAGAGTGAGA[C/T]TCTGTCTCAAACAAC | 11124 |
rs144432213 | snp | C/G | 0.153665 | 0.230694 | intron-variant | FAF1 | GRCh38.p7 | 1:50888048 | TTGTATCCTCTTTTA[C/G]TTCATTGAGCAGTGG | 11124 |
rs144448396 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50792335 | CAGATTGTAGAATTA[C/T]GGTGAAAGTTGAATA | 11124 |
rs144462725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50613736 | CTCAATATACATGTG[C/T]TTATTTACTGGTTCT | 11124 |
rs144471726 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50548689 | CTGTCTAATTTTTAG[C/T]AAACTGTACTTTTTA | 11124 |
rs144489397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50763719 | CATCAGAGTAAATTA[C/T]TGATATCACATAATG | 11124 |
rs144495538 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958509 | GGCGAAACCCTGTCT[C/T]TACTAAAAATACAAA | 11124 |
rs144500896 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50681190 | TAGCTAGGATTACAG[A/G]TGCCTGCAACCACAC | 11124 |
rs144510202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897768 | CATTCACTAGGCTCA[C/G]ACATATGACTTTACT | 11124 |
rs144526265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660404 | AGGGAATTTTAAATG[C/T]CATTCAGGTATTATT | 11124 |
rs144528390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50610974 | CAAAATAGGTTCCCA[A/G]GGTTGAGCTTTGTGC | 11124 |
rs144544448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50532349 | TTAAGATGGAAAAAT[A/G]AACTGGGAATAAGCA | 11124 |
rs144547374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50524687 | TTTGTCAAACATCAG[A/G]TAGTTGTAGGTGTGC | 11124 |
rs144558935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884093 | CTGCACCACTGCACT[C/T]CAGCCTGGGCAACGG | 11124 |
rs144563835 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50830901 | CCCATTTGGAAGAAA[A/G]AAACTTGAAAACCAC | 11124 |
rs144591501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50812210 | ATGACCAATGAGACA[C/T]ATTTAAACTAGAGAG | 11124 |
rs144612283 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50887052 | CCTGCAGTTTCCTGA[C/T]GTTTTTAATGATCGC | 11124 |
rs144616952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603732 | TGCTAGTTACCAAGT[A/G]TACATGCACTTGTCT | 11124 |
rs144618410 | snp | A/G/T | 0.0685596 | 0.171987 | intron-variant | FAF1 | GRCh38.p7 | 1:50736563 | GAGACCAGCCTGTCC[A/G/T]ACATGGTGAAACCCC | 11124 |
rs144618701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685421 | GGTAAACTACTGCTA[C/T]AGTATATAGTATAGT | 11124 |
rs144623728 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50825713 | CTAACAAATCCAGAC[C/T]AGGCATTCTTTTCAT | 11124 |
rs144633136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50557461 | TAATAATTACCTGAA[C/T]ACATCAGAAACAGGA | 11124 |
rs144651812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50946548 | TCTTCTTCCAGAATG[C/T]CACGTGTCTGTCAAC | 11124 |
rs144660505 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50686885 | CCACGCTGGAGTGCA[A/G]TGGCGCGATCTTGGC | 11124 |
rs144662071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50613167 | GTCCTATAATCCAAG[A/G]CCTGGAAACCACTCC | 11124 |
rs144662449 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50697944 | TGTATAACACTGAGT[A/C]ATACACAAGACACAT | 11124 |
rs144672389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50651124 | AAGATTATAAAAGAA[C/T]TGATTACAAGAGGTC | 11124 |
rs144672946 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50492573 | AAGTATAGCCAATAT[A/G]CATATACTTAGCTTT | 11124 |
rs144686975 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50607444 | GTCTGATGTTCAAGG[C/T]CATAACCCTGCCCAC | 11124 |
rs144687272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50838123 | ATCAAATCATAAAGG[C/T]ATGCACAGCTTTTTA | 11124 |
rs144693793 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50512770 | TTTCTAATTCTGTGA[A/G]GAAAGTCAATGGTAG | 11124 |
rs144696218 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50746801 | TTCACAGACCTTCAC[A/G]GCAGCCCCTGCCATC | 11124 |
rs144699454 | in-del | -/CA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50959622 | TTCTCCATAGCTCGC[-/CA]CACACACACACACAC | 11124 |
rs144705156 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50625474 | CAATGTGGTTAAGTC[C/T]CACAATCAATGCTTT | 11124 |
rs144736404 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50566418 | GATGTTACGGCCACA[A/T]GTGTAATTAAACATG | 11124 |
rs144737888 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50645784 | GGTGAGCTGAGATCA[C/T]GCCACTGCAGTCCAG | 11124 |
rs144746515 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440817 | CCTAGGTAGAACCTG[C/G]AGACCCAAGGCAGCA | 11124 |
rs144758961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50910984 | AGCTACAGACTGGAG[C/T]TGTTCCTATTTGGCC | 11124 |
rs144759507 | snp | A/C/G | 0.0127132 | 0.078853 | intron-variant | FAF1 | GRCh38.p7 | 1:50623529 | CAGTGAGCTGAGATC[A/C/G]TGCCACTTGCACTCC | 11124 |
rs144765499 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50541312 | AATACACATTCAGAA[A/G]AGCAATAACCAGACC | 11124 |
rs144776873 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50911504 | AGTTTGAGACCAGTC[C/T]GGCCAACATGGTGAA | 11124 |
rs144800872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50664429 | AACTTGGAAGATATC[G/T]ATATATGTCAGATAA | 11124 |
rs144803915 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50751357 | TTGTTTGTTTTGAGA[C/T]GGAGTCTCACTTTGT | 11124 |
rs144812012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632252 | TTACCTTTCTTAGTC[A/T]GAATTACAAATATTT | 11124 |
rs144817604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50583091 | TTTAAAAGTCTCCAT[A/G]TTATATTTCAACAGA | 11124 |
rs144820852 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674048 | CTCCGCCAGCCAGGT[G/T]CAAGTGATTCTCCTG | 11124 |
rs144826736 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50620952 | TTTGTTAGGTGTTCC[A/G]GGCCATGGGGCCCCC | 11124 |
rs144826891 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50758446 | CCCTTTCCTATTCTT[C/T]ATGTTATTGTTGTCA | 11124 |
rs144835705 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50493493 | ATTTTAATTTGACCT[C/T]ACTTTCCTGACTTCA | 11124 |
rs144840217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50955611 | AAAATAGAATGACTA[C/T]GTGATCCAGCAATTT | 11124 |
rs144866488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956672 | AAATGATTTGAGCCG[A/G]GTGCGGTGGCTCATG | 11124 |
rs144872404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50702122 | TGCAGTAGTAAGGCC[A/G]ATAACAAAGAATCAG | 11124 |
rs144877387 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50584375 | ACAAGTATCGGTCAC[A/G]GAAAGTACACCTGTT | 11124 |
rs144880911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50883833 | ACAGTATTGAGTATA[C/T]GGGAAATTAGGCCAG | 11124 |
rs144889802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50956233 | TGGGGTAATATTTGC[C/T]TTGTAATAAATTCAC | 11124 |
rs144892913 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50839923 | CTATGAACAAACCCA[C/T]TCCTCAAAGCCATAG | 11124 |
rs144909238 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50718034 | ATTTATTTATTTATT[C/T]ATTGAGACGGAGTCT | 11124 |
rs144910825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50628791 | GCATGCTCATCATGA[A/G]TTGCTACCCAGTGAA | 11124 |
rs144911656 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50490919 | CTTTGATAGCTCTGG[A/G]TAAAGTGGCATTCAA | 11124 |
rs144912793 | snp | C/T | 3.31066e-05 | 0.00406844 | missense | FAF1 | GRCh38.p7 | 1:50567131 | GTTATAAAATTTTGA[C/T]TCAGATAAGAAACAA | 11124 |
rs144920776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50915899 | AGTGGACAAGCAGGA[A/G]CCTTTAAAAATCCTT | 11124 |
rs144934108 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50854450 | TGAAAAATGGTAACA[C/G]TCAGAGGGAGATAAC | 11124 |
rs144939896 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750536 | CTGCCCCTACTCACA[A/C]TGATCCTCCTTCTCA | 11124 |
rs144951685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758594 | GTAACCAAATATTTA[A/C]AATTTCTAGTGCTCT | 11124 |
rs144956187 | snp | C/G | 1.65833e-05 | 0.00287948 | missense | FAF1 | GRCh38.p7 | 1:50583665 | ACCTTGAAGAAAACT[C/G]TGCTGTAAATTGTAA | 11124 |
rs144958707 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50443088 | CCTCTGCTTCTCATT[C/T]GTTGGCATTTTCTGC | 11124 |
rs144974401 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50441940 | TTCCTCTTAGAACTA[C/T]ATTATAAACTGTAGA | 11124 |
rs144988159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502898 | GACCATAGCTCACTG[C/T]AGTTTTAAACTCCTG | 11124 |
rs144992818 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50805627 | TACAAAACAGTGGCA[A/T]GTAATATAAATCATA | 11124 |
rs145001798 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50905702 | GAAGTGTCTGTTAAT[A/G]TCCTTCACCCACTTT | 11124 |
rs145002024 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50849022 | CCAGAACTTTGGGAG[G/T]CCAGGGTGGGTGGAT | 11124 |
rs145005084 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50661676 | AAATAACTGCATTGA[A/G]CAAATAAGTATTTGT | 11124 |
rs145005087 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50717609 | CAGCACAGGCTTCTA[A/C]TGTACAAATCCAAAT | 11124 |
rs145015687 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50755329 | CAAAATCCAGCAGGG[A/C]AGTCAAATCTTAAAG | 11124 |
rs145032324 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50629623 | CCTTTAGTCAAACAC[A/G]GGTCAAGATCCCTTT | 11124 |
rs145033025 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50492260 | GACTGGGAGGGAGAA[A/C]AAAGACTAGGAAGTA | 11124 |
rs145053157 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50892384 | AAGCCCCAGTGAGAT[A/G]AACCTGGTACCTCAG | 11124 |
rs145057107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858943 | AAAGTAAATTAACCA[C/T]AATTAAGTATACTTC | 11124 |
rs145057250 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50798830 | GTGGAAGACAGACAT[G/T]ATGTACATGTATTGG | 11124 |
rs145063622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624473 | TTTCTAGTGTTCTTG[C/T]AAAAGTAATTTATCT | 11124 |
rs145069376 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50712341 | TCTGAGGAGAGGGGT[A/T]AGTGGGGAAGGCTGT | 11124 |
rs145092935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50535144 | CACCCCAAATCTAGC[A/G]AAGTGTAAATAGTAC | 11124 |
rs145095095 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50589829 | TTACAGTTAGGTCTT[C/T]CATATATTTTGAGTT | 11124 |
rs145109262 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50443000 | GAGGGGCAAGCTGCT[A/G]GCAAATGTTTACCCA | 11124 |
rs145130327 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50691987 | TTGGGAGGCCCAGGC[A/G]GGCAGATCACTTGAG | 11124 |
rs145143396 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519374 | GGAAGGAAGGAAGGA[A/G]GGAGGGAGGGAGGGA | 11124 |
rs145146268 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50664755 | GTCGAGATCGCGCTA[C/G]TGCACTCCAGACTGG | 11124 |
rs145149567 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50900712 | ACATTTCCCTTTCAG[C/T]TAAATACAAAGGTTT | 11124 |
rs145151337 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50771639 | AGCACACTGGCTCAC[A/G]CCTGTAATCCCAGCA | 11124 |
rs145160481 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50584189 | CCATTATTATTTTAG[G/T]GGTCATTTTGCACGT | 11124 |
rs145192275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932246 | ATTTCAGCATTAACC[C/T]AAAAGTCCACAGTCC | 11124 |
rs145213135 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50780911 | TGGCTCAGCAGGAAG[C/T]AGACAGGGCCAGAAT | 11124 |
rs145224494 | snp | C/T | 8.2498e-05 | 0.00642201 | missense | FAF1 | GRCh38.p7 | 1:50582620 | AAACTGTACTTACAT[C/T]TCGGGCTTTCACATA | 11124 |
rs145228378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50854085 | GGTCTGAAAAGCCAG[C/G]GCTCTTCATTCAATT | 11124 |
rs145232684 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50937478 | GAGGTAAAATTTTAT[C/T]AGCTGCCTTACAAAG | 11124 |
rs145232772 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50604517 | TTCTTTTTCTTCTTT[C/T]TTTGTTTTTTGAGAC | 11124 |
rs145243806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50639241 | TTTGTCTACTATAAA[C/T]AAAGCTCCAATAAAA | 11124 |
rs145244943 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729038 | TATCTATCTATCTAT[A/C]TATATATATATATAT | 11124 |
rs145246081 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459527 | CTTTTTAGTTGTTCA[C/G]GCTGGAGACCTCTAA | 11124 |
rs145254959 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50522878 | CATTCTCATTACTCA[A/G]AAAGAAACTCTGTAC | 11124 |
rs145262426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50878149 | CACCCAGTCTGTGTA[C/T]GCCCCAAACTGCAAT | 11124 |
rs145282525 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50775757 | TGTAACAAAGGGGGA[C/T]GAAAAAAAAAGGAGA | 11124 |
rs145283686 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874324 | ATACCCTGGTATACC[C/T]TCCATCAACACTTCA | 11124 |
rs145284159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467553 | CTCCTGACCTCGTGA[C/T]CTGCCCTCCTCGGCA | 11124 |
rs145294781 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50936839 | AGAGAAACATGGAAT[A/C]ATCTAGAATAAAACA | 11124 |
rs145294847 | in-del | -/TGATG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50856881 | AAACATTAAAAAGAA[-/TGATG]AACAGCCACAATTAA | 11124 |
rs145295249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50691683 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 11124 |
rs145301607 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50602589 | CTCACTGCAACCTCC[A/G]TCTCCCAGGTTCAAA | 11124 |
rs145320522 | in-del | -/A | 0.084364 | 0.187256 | intron-variant | FAF1 | GRCh38.p7 | 1:50653185 | AGCAAGAAAAACAAC[-/A]AAAAAAAAACCACAA | 11124 |
rs145330378 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50827220 | AAAAGAAAGAGAGAT[C/G]AGATTGTTACTTTGT | 11124 |
rs145341060 | in-del | -/C | 0.287085 | 0.247234 | intron-variant | FAF1 | GRCh38.p7 | 1:50573979 | TAAAAATACAAAAAA[-/C]ATTGGCTGGGTGTGG | 11124 |
rs145342630 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50739142 | ATATATAATATATAC[A/G]TATATAGGGGAAATA | 11124 |
rs145356587 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50921993 | CTAACATGGTGAAAC[C/G]CCGTCTCCACTAAAA | 11124 |
rs145364678 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50834934 | TATAAAGACTTCCTA[A/T]AGGAACTTACTCTTT | 11124 |
rs145367376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648519 | ACCTGGAAGGGAAGT[A/T]TCAGACTAAAGAATG | 11124 |
rs145368997 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50471722 | TATCAGTGGACTCTT[-/A]AGAGTTCATCTGCCA | 11124 |
rs145376218 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | FAF1 | GRCh38.p7 | 1:50822763 | TTCTTTCTTTCTTTC[A/T]TTCTTTCTTTCTTTT | 11124 |
rs145385808 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50732699 | AGTTTCTGTCTTTAA[C/T]AGGAGAGTTTAGTAC | 11124 |
rs145402421 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50647403 | ACGTCACTTTCCTTT[C/T]TTTGTCTATAAATTT | 11124 |
rs145414409 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50555976 | TATGTGTATATATTA[C/T]ATATATGGTGTGTAT | 11124 |
rs145416254 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50608836 | TCCTGGCTCTGCTGG[G/T]TAAGAGCTTGTATGA | 11124 |
rs145418394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464783 | ATGACATTATCCTCA[C/T]TTGAAAGATGAAGTA | 11124 |
rs145424086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50909244 | TCTGCCCAGAGATCC[A/G]CTGTTAGTCTGATGG | 11124 |
rs145429431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779442 | GTATTTCTTGAATAA[C/T]AAGACTTGAAATTTG | 11124 |
rs145430140 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662221 | TTTCCAGAAAACAAT[G/T]AAGATCTGTTTCAAG | 11124 |
rs145436707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50656979 | ATTTTAGGAGGTCAA[A/G]GTACAAGGATCACTT | 11124 |
rs145439660 | in-del | -/TAA | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50646069 | ATATGTTAACCCATG[-/TAA]TAATCTTCACAATAG | 11124 |
rs145443109 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50586619 | CCTGCCATCTTAACT[C/G]TACTTCTCACGGAAA | 11124 |
rs145446981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495997 | GATGACTATTAAAAA[C/T]AAAATATTTTATGAG | 11124 |
rs145451510 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50450318 | TACTCCTATTATTTC[A/C]ATTTTACAGATGAAT | 11124 |
rs145465698 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | FAF1 | GRCh38.p7 | 1:50888778 | TGCCAGTATTTTATT[C/G]AGGATTTTTGCATTG | 11124 |
rs145471828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50793527 | TAATAGAAAAAAACA[C/T]ACTCGGTAACTGGTA | 11124 |
rs145473196 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50686204 | TAGTTCAACATAACT[A/G]CCATCTAATAGTCAG | 11124 |
rs145479338 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50605209 | AAGAGCTGCTCACTG[G/T]AACAGAATTAGCACA | 11124 |
rs145479601 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50671587 | ATTTAAGAGGGTGAG[A/G]ATTCAAACTTAATCC | 11124 |
rs145481911 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50591023 | GGGTCATTCTTATCT[C/T]GTTCCTGATTTTAGA | 11124 |
rs145503800 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50876170 | ACTTGAGCAGGCTTC[A/G]TGCTTCTCAAGATGA | 11124 |
rs145506765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50720190 | TATTTTTAGTAGAGA[C/T]GGGGGTTTGCCATGT | 11124 |
rs145533324 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50583261 | TCCAAAAGAAAAAAA[-/T]AAAGGAAAAAATTCA | 11124 |
rs145539547 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917390 | GCAAGAACTTGAAAA[C/T]ACAGGCTTTGCATCA | 11124 |
rs145556931 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50539440 | ATATTATTTTTTATA[A/G]CACCTATATTTTTTG | 11124 |
rs145567954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50800696 | ATATATGGTTTCTTA[A/T]CAAGAACAGCATGTC | 11124 |
rs145572120 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50713075 | TGAGGTGGGAGGACC[C/T]CTTGAGGATAGAAGG | 11124 |
rs145582416 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50594629 | ATTTGGGAGGCCGGG[G/T]GGGGTGGGGGTTGGG | 11124 |
rs145595333 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50444867 | CTAAAGCTGATGATA[C/T]GAATGATTCTGACTA | 11124 |
rs145595373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502144 | CAGTGGCTTTCACAT[A/C]AACTTTAAGCCAATC | 11124 |
rs145605798 | in-del | -/T | 0.297128 | 0.245518 | intron-variant | FAF1 | GRCh38.p7 | 1:50448372 | TATAAAATTGAGACC[-/T]CTTTTTTTTGCCTCC | 11124 |
rs145639809 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50483905 | GAGCAGGTTTGGGTG[G/T]GGAGGGTAGGATCAG | 11124 |
rs145648822 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50944861 | TGGTCAGGGTGGAAT[C/T]CTGAATTCTCAAAAT | 11124 |
rs145649633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881634 | GTTGAAAGTATCAAT[C/T]GGGAAGACCCTTGGC | 11124 |
rs145654796 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50715308 | TTTTAAAATTGAAGG[C/T]GGCGGGGTGGGAGCC | 11124 |
rs145655631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50802563 | TAACAAGTTACCAAG[C/T]AGTCAGAACATAGCA | 11124 |
rs145659095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955154 | AAGTTTCAGACCAAA[A/T]GATTCATGTTCTCTA | 11124 |
rs145670724 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50537739 | TAATAGAAAACAACC[A/G]TATTCTGTATTCTCG | 11124 |
rs145696905 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50667784 | AAAAGATTTTTTTTC[A/C]TTGAAGAAAAGACCA | 11124 |
rs145712305 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50560384 | ACCTGAAATACCACA[-/C]CCCAAGGGCATTAAG | 11124 |
rs145743677 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50899108 | TATACAAGTTCACTA[C/G]TATACAAGTTCACTA | 11124 |
rs145750554 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766509 | AGCCAGGATGAACAT[C/G]TGCTGCCACCAAGAG | 11124 |
rs145754920 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50682826 | TGGCCGGGCGTGGTG[A/G]CTCAAGCCTGTAATG | 11124 |
rs145761206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619193 | CTTTTTATTCAGTTT[A/G]TCATTCTGTGTCTTT | 11124 |
rs145761389 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50478277 | CAAGCGATTCTCCCA[C/T]CTCAGCCTCCCGAGT | 11124 |
rs145774050 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50474286 | CTTTAGAGGTAATGT[C/T]CCTTAAATGACATGA | 11124 |
rs145783351 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 1:50822300 | CAAGACTGGTCCAGA[C/T]GAAATTAAACACAAG | 11124 |
rs145793666 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50739320 | TACATGCATATACAT[A/G]TGTACATGTGTACAC | 11124 |
rs145795226 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50519454 | GGAGGAGGGAAGGAG[A/G]GAGGGAAGGAAGGAA | 11124 |
rs145798814 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50618917 | CCATACCACCATGCC[C/T]GGCTGATTTTTGTAT | 11124 |
rs145801777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534671 | AAGTGTCTATTTACT[A/G]CCATAACACTGATTG | 11124 |
rs145816188 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50886335 | TTTGAAGGATATTTT[C/T]ACTGAATATTTTATA | 11124 |
rs145840783 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50652286 | GCATGACAACTCTTT[A/G]GCAAAAAATTAAATG | 11124 |
rs145846654 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | FAF1 | GRCh38.p7 | 1:50739336 | TGTACATGTGTACAC[A/G]TACATGCATATACAT | 11124 |
rs145849599 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50906276 | ATGCTGTTTTGGTTA[C/T]TGTAGCTTTGTAGTA | 11124 |
rs145872450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469733 | TAATTTGGGCTATGA[C/T]GACTTGGGCAGTGGT | 11124 |
rs145873677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50481627 | ACACATTTTCCCATC[C/T]TTAGGTGATACAAGA | 11124 |
rs145880404 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50940427 | ATACCATTATGTTTC[C/T]GTTGTTCATTTGTTT | 11124 |
rs145881557 | in-del | -/ATA | 0.118584 | 0.212673 | intron-variant | FAF1 | GRCh38.p7 | 1:50865834 | CCTAAAACTTAAAGT[-/ATA]ATAATAATAAAAGAA | 11124 |
rs145882984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50948040 | TGATCACTGACAATC[C/T]AACATAAGACTCAAA | 11124 |
rs145888025 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50828318 | CTGTCACCCAGGCTG[A/G]AGTGCAGTGGCACGA | 11124 |
rs145895825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50856736 | AATAGGTTAAATATG[C/T]AACATGTATATGCAG | 11124 |
rs145897491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50574209 | CTTTATCAGTTTTCA[C/T]TGCTTAGACTGTAAT | 11124 |
rs145901427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50483938 | GTGCAATTTAAAACA[C/T]ATTAAGTTTCTGATG | 11124 |
rs145904844 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50938701 | CTACTAGGATTTTCC[-/T]GGTTTGAGGTCTTTC | 11124 |
rs145914812 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466250 | TTGGAGAAAGGAGAG[A/G]AAGAGGAGTCAAGGA | 11124 |
rs145920112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744401 | TTTGAGAAAAAGGTA[A/G]AGCCTCTCAAAAAAA | 11124 |
rs145925459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50658741 | TTGGCTGAGAGAGTC[C/T]CATGTAAAGCATATT | 11124 |
rs145929466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50685150 | GAAGAGCTGAGGGAA[C/T]TACATGAGCAAGAAA | 11124 |
rs145932552 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50603173 | GATAACCAGTAATTA[C/T]TTTCTTTGGCTTAAT | 11124 |
rs145937888 | in-del | -/AACA | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50895578 | AAAACAAAAACAAAT[-/AACA]AACAAACAAACAAAA | 11124 |
rs145948617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681531 | TCTTTTTTTGAGACA[C/G]AGTTTCACTCTTGTT | 11124 |
rs145950928 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50598827 | TACAAAAAATTAGCC[A/G]GGCATGGTGGTTCAT | 11124 |
rs145959438 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466438 | ACTGAGTAGATCGTT[G/T]TATGTAGAAATGTTT | 11124 |
rs145969799 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50534463 | CATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 11124 |
rs145973798 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50552390 | AGCTAGAATTCCAAT[A/C/T]GTGGTCTGAATAAAT | 11124 |
rs145978489 | snp | A/T | | | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461686 | AGGAATATTTCCAAT[A/T]ATGAAAGAAATCTGC | 11124 |
rs145985989 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50727226 | GAAAGTACTCACTAT[C/T]ATCTGATATTTTTTC | 11124 |
rs145987062 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50818297 | CATTACTGGTGGGAA[G/T]GTAAAATGGTGCAGC | 11124 |
rs145987817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50878715 | ATGCCCATTAAAATC[A/C]TTACACATTAAAAAC | 11124 |
rs145993258 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50889974 | GTGGGGTGTTAAAGT[C/T]TCCTATTATTATTGT | 11124 |
rs146001895 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50950813 | CAGCCAAGCACTGCT[A/G]ATTTATTTTATACGT | 11124 |
rs146022206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50795337 | CTGACAGCAATGCAT[C/T]TGTCAGGACCACCAT | 11124 |
rs146028601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50731166 | ACAAGTTTCCTGTGT[A/G]AGGGACCCTCTGGTC | 11124 |
rs146043680 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50953695 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTACAG | 11124 |
rs146049338 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50710449 | CTTTGACCTCGACAA[C/G]TCATTCATTCTTTTT | 11124 |
rs146053323 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50572953 | ATCCTCCTGACCTGG[C/G]CTCCCAAAATGCTGG | 11124 |
rs146053689 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50622000 | GTGAAACCCAGTCTC[C/T]ACTAAAAATACAAAA | 11124 |
rs146055233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50480648 | AAAGATAGTATGTGC[C/T]ACATAGGGACTTTTC | 11124 |
rs146067827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50706560 | GAAATGTAAGTCATG[A/G]TTCTATTTTTATCTC | 11124 |
rs146069603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50615348 | ACTGCAAGTGTCATT[C/T]TGGTACAATAATCTA | 11124 |
rs146073903 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50618071 | TAATCTAGCTAGTAG[C/T]CTATCAATCTTGCTT | 11124 |
rs146080867 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50953988 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 11124 |
rs146096872 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576262 | TCATGTTTTTTCCAT[A/G]TTAGACATAGGCTCA | 11124 |
rs146098227 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50487875 | CTGATCCAGATTAGG[A/T]GTTCAACCAGTTTGG | 11124 |
rs146099851 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951530 | GGTCAAAGATCACCA[A/G]AAGAGTCAGTGGTAG | 11124 |
rs146107170 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50747074 | GCAGAAGCCCTCATG[C/G]AGAATCTCTACTAGG | 11124 |
rs146123501 | snp | A/G | 0.029116 | 0.117091 | intron-variant | FAF1 | GRCh38.p7 | 1:50891263 | GTTAGCCATTCGTCT[A/G]TCTTTTTTCAAGGTT | 11124 |
rs146146318 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50844741 | TATTTTCCAAGTCAC[A/G]TTATGGGTATGAGAT | 11124 |
rs146150374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50751213 | GCTTTGTAAACTTGA[C/T]AGAGGGCATTGCTGA | 11124 |
rs146165467 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50895759 | AATCAATCTATGTGA[C/T]ACATCATATCGACAG | 11124 |
rs146174806 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50730821 | CTTGAACTTCCCTTA[C/T]ATATATTGCTAGTTG | 11124 |
rs146177041 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50592978 | TGATTGTCTTAAAAC[A/C]CACAAAGTCATGTAG | 11124 |
rs146177334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505889 | ATTTAAAGTTTAGAA[A/T]ATCTAGGGAGAGCTT | 11124 |
rs146177591 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | FAF1 | GRCh38.p7 | 1:50644887 | GCTTGTAAGTTTCCA[A/G]CTGGGGCTGTCTTGC | 11124 |
rs146182378 | in-del | -/CTTTT | 0.0444908 | 0.142359 | intron-variant | FAF1 | GRCh38.p7 | 1:50645008 | GAATTCATTTCACAA[-/CTTTT]CTTTTCTTTTAAACC | 11124 |
rs146184283 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50749279 | ATCTCCAAGACCTGA[A/C]ACCACCTTCTTACAC | 11124 |
rs146196147 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50638817 | CAGTTTGCTAAGTTA[C/G]TTTGCTTTTGCTTTG | 11124 |
rs146218618 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50598058 | CAGCACTTTGCAAGG[C/T]TGAGTCAGGAGGATA | 11124 |
rs146219715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50511271 | TGAGATTTTATTATT[A/G]TACTTTAAGATCTGT | 11124 |
rs146231469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50765451 | ATTTCTAGAAGGCAA[C/T]TAAACATTAAGGATA | 11124 |
rs146234971 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50681854 | TTTTTCCTCTTTTTG[A/C]GACAGGGTCTTGCTC | 11124 |
rs146249787 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50821616 | GAGCATAATTTTGAG[A/G]AAGTTACTTAGTTTC | 11124 |
rs146272496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770690 | GCCCAGAGCAATTTA[C/T]AGATTCAATGCTATT | 11124 |
rs146272945 | in-del | -/GAG | 0.0704396 | 0.173948 | intron-variant | FAF1 | GRCh38.p7 | 1:50573681 | TCAGCTACTGAAGAT[-/GAG]GAGATGCCAGGATGG | 11124 |
rs146278651 | in-del | -/GGGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50586161 | ATCTGTCATCGGCGG[-/GGGT]TTTTCTAACTTATTT | 11124 |
rs146285557 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50913830 | AACTTCCTAGACTTA[C/T]TATGGCCTGAGTAAA | 11124 |
rs146298321 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50582020 | AGATCACAAAGTCCA[C/T]TTCTATGTTTAAAAC | 11124 |
rs146298340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50528842 | CCTCAGCCTGCTCTA[C/T]GTGAAGGTGACAAGA | 11124 |
rs146311731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50660280 | CTCAAATGAGTTGTT[C/T]TAAACTATTTTTATA | 11124 |
rs146316493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50577072 | GCAATGCAACTCCGT[C/T]CTGCATTTTTTTGCT | 11124 |
rs146323732 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50947094 | CCTGACATATACAAA[A/G]TAACCAAAAGCTAGA | 11124 |
rs146327938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639568 | CTGAGATAAATCCCA[A/G]TGATGATGCATAACT | 11124 |
rs146339474 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50534359 | GATCTTGGCTCACTG[C/T]AACCTCCACCTCCCA | 11124 |
rs146349863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850210 | CAAAAAACTTAGAGG[C/T]AGAAATACATACGGC | 11124 |
rs146351343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50791856 | CATGTTTCATTTTCC[C/T]GATTGGATCCTGATA | 11124 |
rs146354467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50707418 | AATTAAGCATAATGG[G/T]CTGGGTGCACTGGTG | 11124 |
rs146364766 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461129 | TATACAATATAACTA[C/T]TGTGAATAATGGGAA | 11124 |
rs146366388 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50930772 | CGTGCCACTGCACTC[C/T]AGCCTGGGAGACAGC | 11124 |
rs146370279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50845344 | TGCAGTCTTAGCCTA[C/T]CAATAACCTTTCCAT | 11124 |
rs146380968 | in-del | -/A | 0.0314385 | 0.121371 | intron-variant | FAF1 | GRCh38.p7 | 1:50711269 | ACTTACTGAAAACAG[-/A]ACACTTTTGAAGGGT | 11124 |
rs146406296 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50935036 | ACTTGGTATTCACTA[A/C]GCTTCTTAAATCTGT | 11124 |
rs146420986 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458295 | CATTTTATGTTCAGC[A/G]TAGTATGGGGAAAGG | 11124 |
rs146426576 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50927471 | CCTGTAGTCCCAGCT[A/G]CTTGGGAGGCTGAGG | 11124 |
rs146438793 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50545458 | ATTTTTAGTAGAGAT[A/G]GGGTTGCACCATGTT | 11124 |
rs146446625 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | FAF1 | GRCh38.p7 | 1:50739342 | TGTGTACACGTACAT[A/G]CATATACATGTGTAC | 11124 |
rs146451627 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50636709 | GTTGCCAATTGTAAT[A/G]AAGTCCAATTTATCC | 11124 |
rs146453675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652343 | TCATAAAAGACCATG[C/G]CAACTCAATTCAATG | 11124 |
rs146467249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786489 | TCCAATGGGTACAGA[C/G]TTTCAGTTATGTAAG | 11124 |
rs146478813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50591438 | AGCACTTTGGAAGGG[C/T]GTGGCAGGTGGATCA | 11124 |
rs146491313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723244 | CATCTCTACTACAAA[C/T]ACAAAAATGAGCCAG | 11124 |
rs146491590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50812862 | AAAGAAAATATGGTA[C/T]ATTTAGACCACAGAA | 11124 |
rs146503096 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50454803 | GTTATCTGTTGTGCC[C/T]TTTGATTATTTGTTT | 11124 |
rs146508131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50923222 | CCAGGAGTTCATGAC[C/T]GGCCTGGGCAATATA | 11124 |
rs146510209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50922674 | AAATACAAAATTATC[C/T]GGGTGTGTTGGTGCA | 11124 |
rs146514804 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50677871 | TTGCACTCCAGTCTG[A/C]GCAACAAGAACAAAA | 11124 |
rs146520494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50540768 | AAAGACCAAATGCAA[A/G]TATAGAATGCTTTAA | 11124 |
rs146520575 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50593917 | TATAGGCAGTTTAAA[G/T]AAAAATGAGCAACCA | 11124 |
rs146520775 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50451237 | AAGGGGAGAAAAGAT[G/T]AAAGTAAGAGAGGAA | 11124 |
rs146543533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50947434 | ATTCCCCCATAACCA[C/T]AAGTAAATATAAAGC | 11124 |
rs146555629 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50641708 | CAAAGTTGATTAATC[-/A]TGTTGGCCAAATCTA | 11124 |
rs146559295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50566952 | GCAACGAGCAGCTTT[C/T]GTCTAATGAAATGCA | 11124 |
rs146570464 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50819389 | GGAGATTGAGGAAGG[G/T]AGATCGAGTGAGCCT | 11124 |
rs146570520 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50758457 | TCTTCATGTTATTGT[G/T]GTCATACCTGTACTT | 11124 |
rs146576083 | snp | C/G/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50674087 | TCCCAAGTAGCTGGG[C/G/T]TTACAGGCGTCCGCC | 11124 |
rs146589134 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50813368 | AAACCATTGCTAATA[C/T]TTTAGTGTATATCCT | 11124 |
rs146595957 | snp | C/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50610995 | AGCTTTGTGCAGCAT[C/G/T]TGAATTATGCAGGAA | 11124 |
rs146621760 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50944958 | CCTTTTCTGGGGACA[A/G]CTACAATCAGTGGCA | 11124 |
rs146622531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50474764 | AATCTTATTTTTCAT[A/C]ATCTATAAATCTGAT | 11124 |
rs146626546 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50507669 | TACAGTGAGCTACCA[C/T]CATGTCACTGCCTTC | 11124 |
rs146640399 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470140 | TATTAGAGGTATTAC[C/T]ATAGGAAGGTTTTTG | 11124 |
rs146662319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916959 | TAGCCAAGTCCTAGG[C/T]AACTGGCAATGAGAG | 11124 |
rs146678495 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50501791 | AACACTTCGGCAGTT[C/T]GTTAGAAAGTTATGC | 11124 |
rs146685381 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927261 | TTTATGTTATGTATA[C/T]TTTACCAGAATTTTT | 11124 |
rs146690254 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50839611 | AGGTGTTCTACACAA[C/G]GAGACTTATGACCTG | 11124 |
rs146690968 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50780506 | ACAGGGACTCACTTT[C/T]TCATCCCCTGGGTAC | 11124 |
rs146693350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50693150 | CTAACCCAAAAACCA[C/T]GAAAAATTTTTCCTG | 11124 |
rs146700924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454262 | AGCAGTTTGCTATTC[C/T]TCAAATATGTCTTGT | 11124 |
rs146704413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50823567 | TTTTAGATCATAACA[C/G]TGAACATAAGGTAAA | 11124 |
rs146708827 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50836104 | GAAATAGGATGTACA[G/T]AAATACTCTCTCTGT | 11124 |
rs146710835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50763023 | CACTTTGGGAGGCCA[A/G]GGCAGGTGATCACCT | 11124 |
rs146715768 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50629327 | GGTGCATGGCACCAC[A/G]CCCAGCTAAGTGTTG | 11124 |
rs146716599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50546022 | AAATAAAAAAATTAG[C/T]TGGCAAGGTGGCATA | 11124 |
rs146759028 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50634357 | AAAACCCAAGGGTCT[A/G]AAAGTACAACTTAAT | 11124 |
rs146759231 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50549385 | ATGATCATAGCTCAC[A/G]GAAGGCTTGAACTCC | 11124 |
rs146759237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50495084 | GAAAGTGGGGTGTCC[A/G]TCCCCTCAAGCACTT | 11124 |
rs146797267 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50909343 | TTGGTGAATCTGACA[A/G]TTATGTGTCTTGGAG | 11124 |
rs146810495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808232 | AATTTGTTACCACTA[G/T]ACCTGACTTACCAGA | 11124 |
rs146811782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50867224 | CTAAAACCTGAAACC[A/G]TACAACTCAAGAAGA | 11124 |
rs146823325 | in-del | -/TTTA | 0.422787 | 0.180679 | intron-variant | FAF1 | GRCh38.p7 | 1:50717988 | TCAAAAATACAATCC[-/TTTA]TTTATTTATTTATTT | 11124 |
rs146824758 | snp | C/G | 1.67739e-05 | 0.00289597 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50738949 | GTGTAGAGATTTTAG[C/G]ACCGTCTGAAAAAGA | 11124 |
rs146825407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944147 | TTCACAGGTGTTTTG[C/G]ATGGAAGGTACATGA | 11124 |
rs146831648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860014 | GGAAAGGACTGCCTA[C/T]TGAATAAACAAACAG | 11124 |
rs146838059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652204 | ACTTAAGAGCACCAA[A/G]TAGTATTACAGTCTT | 11124 |
rs146838994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50568153 | TAACTTCTTGGTACT[A/G]CCTCAAAGAAGAGCT | 11124 |
rs146840879 | in-del | -/AAAAAAAAAACC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50651815 | GTAAGTATAAAAACA[-/AAAAAAAAAACC]CCACCGCCTGCAACA | 11124 |
rs146846920 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50819968 | ATGCTAGAAAAATGC[A/G]ATCTCAGATGCATGT | 11124 |
rs146854843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786065 | TTGAGCCCAGAGTTT[A/G]AGGCTACAGTGAGCC | 11124 |
rs146857605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50699363 | GGTTTTTTTAATCTC[A/C]TAACTTTGGTTAATA | 11124 |
rs146869073 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50905725 | CCCACTTTTTGATGG[G/T]GTTGATTTTTTCTTG | 11124 |
rs146876470 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50655767 | TCCTCCCTCTCTTGT[G/T]TTCAACTCCTGGCTG | 11124 |
rs146881643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50573525 | AAAGAACTCCAAGCT[A/G]GTTATCTTTAAAGAG | 11124 |
rs146881791 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519390 | GGAGGGAGGGAGGGA[A/G]GGAGGGAAGGAGGGA | 11124 |
rs146905973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50631585 | CTTTAAGTGAAAAGG[A/G]GAAAGTTCTTGACTT | 11124 |
rs146906006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50684487 | CGAGGCATTCAGGCA[C/G]AGATGAACTTGAAGA | 11124 |
rs146906401 | in-del | -/G | 0.0225045 | 0.103662 | intron-variant | FAF1 | GRCh38.p7 | 1:50569518 | CCATTAACAAATTCA[-/G]GAACTCTTCTTCTTA | 11124 |
rs146927922 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50577886 | TTGGAAGCTCTGCTT[C/T]GTACAGTACTGTAAA | 11124 |
rs146941488 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50657489 | ATCAGTTGAGCCCAG[C/T]AGATAGAGGCAGCAA | 11124 |
rs146951386 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50861448 | TTAGTGAAATGACCC[C/T]GAAACAGAAAGTCAA | 11124 |
rs146967630 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50909898 | TCGTCAAAGTCATTC[G/T]CCATCCAGCTTTGTT | 11124 |
rs146974867 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704503 | ATTTAGATTTTACTA[C/T]CCTGTAAAATTTCAG | 11124 |
rs146975821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50789389 | AACTCAGTATGTCCA[C/T]AGCTTAGTTCATTAG | 11124 |
rs146976386 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50847642 | TCAGAATCTTAGAAA[C/G]AGGAGAGAGAAAGAA | 11124 |
rs146988679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50928104 | AGCCAGACTGGTTTT[C/T]AGGAACAAGTCACCT | 11124 |
rs146993171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842003 | AGAGTTTTGGACTCT[A/G]TTACACTTCCTGACT | 11124 |
rs146997335 | snp | C/G | 0.0850919 | 0.187897 | intron-variant | FAF1 | GRCh38.p7 | 1:50574898 | AGAGTTGTATTAACT[C/G]TTTTTTTTTTTTTTT | 11124 |
rs147009094 | in-del | -/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50698146 | TTTGGTTTAATTTCT[-/TG]TGTGTGTGTGTGTGT | 11124 |
rs147010602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50709390 | ATAACTGATTACTTA[C/T]CAGTATATCCCTTGG | 11124 |
rs147011128 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50653776 | GAGGCTGAGGCAGGA[A/G]AATCAATCGCTTGAA | 11124 |
rs147012568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793991 | TTAGGAATGCTCAAC[C/T]AACCAGTACGTATAA | 11124 |
rs147033798 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50600231 | AAAGCCTTTGTGATG[C/T]GTTCAGTGGTTATAT | 11124 |
rs147035246 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50455981 | TCAGGAGGCTGAGGC[A/C]GGAGAATCGCTTGAG | 11124 |
rs147046071 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50679595 | CAATAAATGGCACTA[C/T]CATGAACTCAGTTAC | 11124 |
rs147056179 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50887334 | GGTAGGTTGCCTGTT[C/T]ACTCTGATGGTAGTT | 11124 |
rs147056265 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50933510 | TGGACCTTATTGTTC[A/G]TATCACTAATAGTAT | 11124 |
rs147072665 | snp | C/G/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50928599 | CCAGCCTGGCCAACA[C/G/T]AGTGAAACCCCATCT | 11124 |
rs147076437 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50814602 | AAACATTATGCTAAG[C/G/T]GAATAGTTAGATACG | 11124 |
rs147078631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50724694 | TGTTTCTCTTAGTGG[A/C]AAAATAGAGCCAATT | 11124 |
rs147091858 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869714 | TCCAATTTACCTACC[C/T]AGTATAGAGTTTTTT | 11124 |
rs147101877 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50597171 | ACAAACATTACTTTT[C/T]ACTAGTCTGTGAAGA | 11124 |
rs147113869 | in-del | -/GGG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950530 | TGAACGGGTATGGCT[-/GGG]GTGTTGCAATAAATC | 11124 |
rs147114445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50675566 | CTTTGCAAGAAGCCA[C/G]AAGTCAGGAATCCTG | 11124 |
rs147129986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50811546 | TACAAAAGATTGCTC[A/G]AAGGTATCACACATG | 11124 |
rs147141113 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50945899 | TCAGTCTGCATAGCT[A/G]GTACAGAGGCTGAAC | 11124 |
rs147141486 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50897358 | GATTGTCTGTTCCCA[A/C]AATTTAAACATTCTG | 11124 |
rs147146162 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50805735 | ACCCTTAAAGAAAAT[C/G]GCAATGACAAATTTT | 11124 |
rs147168526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671171 | GCACTTTGGGAGGCT[C/G]AGGCAGGCAGATCAC | 11124 |
rs147177766 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50903028 | AACAAAACCTGGGCA[C/T]TTATCAGACTATAAT | 11124 |
rs147187351 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50608655 | CCCAAAATGTCTCCC[C/G]CTATCTCTCAAATCA | 11124 |
rs147188587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521548 | AAAATACTAAGATGG[C/T]TACTTTTTAAATGTT | 11124 |
rs147192696 | in-del | -/GG | 0.021333 | 0.101051 | intron-variant | FAF1 | GRCh38.p7 | 1:50716215 | GGTACAATAGTAGTA[-/GG]CAAACTGTCTTGAAC | 11124 |
rs147201928 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50740527 | AAATGAAAAGAAATA[A/C]ATAATTACCCTTATT | 11124 |
rs147204375 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50908583 | CACATATATTTAGGA[C/T]AGTTAGCTCTTCTTG | 11124 |
rs147204850 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50654009 | ATTATTAAAGTTTCT[A/G]ATTTTTAAAATTTCA | 11124 |
rs147210320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943285 | CAATTTTCAGAACTG[A/T]TTTCAACCATGTTTC | 11124 |
rs147213113 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50556619 | GGTGGACAGATTGCA[C/T]GAGCTCAGGAATTTG | 11124 |
rs147223359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612033 | GAACGAAAACAGTTC[A/G]ATGGTAATCTTGTTA | 11124 |
rs147224371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467668 | TATTTCTTATTTGGC[C/T]CAGGAAGCATGATGG | 11124 |
rs147268445 | in-del | -/TTATTTAT | 0.301281 | 0.248076 | intron-variant | FAF1 | GRCh38.p7 | 1:50557907 | CACTTTATAAATATC[-/TTATTTAT]TTATTTATTTATTTA | 11124 |
rs147270908 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50778021 | TGTTCACAGCAGCTT[C/G]GTAACGCTAGAAAGA | 11124 |
rs147294056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625788 | GTTCCATTAAGGAGT[A/T]TAGACATTATCTTGT | 11124 |
rs147295241 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543096 | AATTTTTCATTGCTG[A/T]AGCATAGATATTTCT | 11124 |
rs147310614 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622624 | TGATCCATTTCATTT[C/G]CTGAAGGACATGTAT | 11124 |
rs147310948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50676495 | TGTAAATATTATTTT[C/T]AATGTAACAATCACC | 11124 |
rs147315718 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50498656 | GGAGTTCGAGACCAG[C/T]CTGACCAATATGGTG | 11124 |
rs147322251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50885405 | TATTCACAATTGTTA[C/T]GGCCTCGCTGAACTG | 11124 |
rs147331905 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50547247 | ATGCAAATGCACATA[C/T]TGTAAGCATGTTGGA | 11124 |
rs147332211 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493181 | GGGATTACACGCACC[C/T]GACATCACGCCCAGC | 11124 |
rs147339564 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50759871 | AGATGGTAACTCATT[C/G]TGGTTTTGATTTGCA | 11124 |
rs147358189 | snp | A/C/T | 3.29511e-05 | 0.00405887 | missense | FAF1 | GRCh38.p7 | 1:50490613 | TCTTCTTGTTCTTTG[A/C/T]GAATCTGCTCCAAAC | 11124 |
rs147358465 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50852482 | AAACAAAGCAGAAAT[A/G]TATTTAGAGTAAAGC | 11124 |
rs147378879 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50627553 | ATCCATCTCATAAAC[C/G]GAAGGTTGGACAAAG | 11124 |
rs147401185 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50565167 | CCTTTTAAATTTGTA[A/C]TATGGACAGAACTAT | 11124 |
rs147412345 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50695050 | GTCAATGTGTAAAAC[A/G]AAATTTTCTATTCAT | 11124 |
rs147413451 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50782862 | CACTCACTGCTCACT[C/T]ATTGAGAGCAACTTC | 11124 |
rs147413681 | in-del | -/TGTGTG | 0.251036 | 0.249998 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460809 | CTAAGTATTTGTATA[-/TGTGTG]TGTGTGTGTGTGTGT | 11124 |
rs147418452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521066 | TAATTGACAAAAATT[A/G]TATATATCATGTATA | 11124 |
rs147437358 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50516668 | CAAAATGGCTCTCAA[A/G]CATATGTAGGTTTGT | 11124 |
rs147457916 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50881393 | CTTTCAAAGTTGTCC[C/T]CCTGGTGAACTCATC | 11124 |
rs147458087 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924260 | ATCGGCAGTACTTCT[A/C]CACACCAAAAAGGAA | 11124 |
rs147482744 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50790813 | TATTTTATATTTAAT[G/T]TCCTTCATACTATTG | 11124 |
rs147485794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50651557 | CCTCACTTTTAATGA[C/G]CTTTATAACCAATCC | 11124 |
rs147485956 | in-del | -/G | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50589073 | GCAAGCACAGTGGTA[-/G]GGGCAGGAGCCAAGG | 11124 |
rs147493334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884764 | TTTTTCTGATTTTGG[C/T]ATCAGGGTAATACTG | 11124 |
rs147503908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50588781 | AGCAACAAAGGGCCA[C/T]GGCTAGCAACAATGA | 11124 |
rs147517574 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50721770 | CTAGGACTACAGGCA[C/T]GTGCCACTATGCCTG | 11124 |
rs147523983 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50542703 | GGCAAACCACTCTAC[A/T]ACAAAGGGAAATGGC | 11124 |
rs147527357 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50920498 | AATCCAGGCCAATTT[G/T]CCTCATGAACATAGA | 11124 |
rs147527508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50453003 | TGATCCTGTCCTGCT[C/T]CTTCTCAAAGTTCTT | 11124 |
rs147540276 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50592655 | AAGTCAACAGCAAAA[C/T]GATTATTGTTGGCTG | 11124 |
rs147543701 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50447389 | CTCGGCCTCCCAAAG[A/T]GCTGGGATTACAGGC | 11124 |
rs147553712 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50614972 | CATGTACAGGATTTT[C/T]ACATGGGTATATTGC | 11124 |
rs147554327 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50664854 | CTATCGTAGGCTAGC[A/T]GAAACAAGGCCCAAA | 11124 |
rs147571054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50661778 | ACTCTGAAAGGCTTA[C/T]AGTTAAGAAAGCAGT | 11124 |
rs147590003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50619084 | ATGTTTTATTTCTGC[A/G]TGGTAGATCTTTCTC | 11124 |
rs147590569 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50535278 | ATCATCCTTATTTAT[C/T]GATCATATCATAGGC | 11124 |
rs147610450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464270 | CCCTGGCCTCTCAAA[G/T]AGTTGAGATTATAGG | 11124 |
rs147612247 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50932314 | ATGAGCCTCTAAAAT[C/T]AAAAGCAAGCTAGTT | 11124 |
rs147615804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847833 | ACAGATCCAAGAGCA[C/T]CAACAGCACCCAAGG | 11124 |
rs147627295 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50517210 | TTTGCAAATCTTTTT[C/T]CCCAGCCCCTGCCCT | 11124 |
rs147627384 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459557 | AGTCACCTCTGAAAA[C/T]TTCCTATCCTCCCGC | 11124 |
rs147632431 | in-del | -/AC | 0.148577 | 0.228502 | intron-variant | FAF1 | GRCh38.p7 | 1:50740835 | GTTAACATGCAAACA[-/AC]ACACACACACACACA | 11124 |
rs147637423 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50799109 | GAGCTACCACGCCCA[A/G]CTCTCAAAGGAAAAA | 11124 |
rs147647466 | in-del | -/TC/TCTCTC/TCTCTCTC | 0.439502 | 0.163061 | intron-variant | FAF1 | GRCh38.p7 | 1:50885295 | CTCTCCGTGTCTCTT[-/TC/TCTCTC/TCTCTCTC]TCTCTCTCTCTCTCT | 11124 |
rs147651901 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794159 | ACAAAAATACAAGGG[C/G]TGCCACCTTGGTAAA | 11124 |
rs147676741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50600667 | TCCAACTATAGATCT[C/G]TAGGAGGTCAGATTT | 11124 |
rs147696085 | snp | A/G | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50556195 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 11124 |
rs147714841 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50488932 | TTTGTCAGGCATAAT[A/G]TCTTGTATATATGTG | 11124 |
rs147730771 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50483414 | CTGCACTCTAGTAAC[A/G]TCCAACTTTGTTTTC | 11124 |
rs147740076 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50732965 | TTTTAAAATACAGAC[C/T]AAAGTTAATCAGTAT | 11124 |
rs147741970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823167 | CAAAGCCATAAAGCT[A/G]TATCTGCTTTATATT | 11124 |
rs147753286 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50955443 | TGTACGTGTAAAACT[C/G]ATTTTTGGTCAAATA | 11124 |
rs147756789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50881945 | TGAAAATTGTAAGAT[C/T]TTTGCTCTTCAGTTG | 11124 |
rs147759484 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50712317 | GCTTAAGTTTTGTTT[G/T]GTGATGACTCTGAGG | 11124 |
rs147775908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50708548 | ATGTCATGTAGAGTT[C/G]AATATAAGACTCAAA | 11124 |
rs147776271 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50757230 | TATAATGAGGAGTAT[C/T]ATATACATTTTAAGT | 11124 |
rs147781350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50619439 | GTCTATTTGAAACAC[A/G]TTCCCTCAGCATTTG | 11124 |
rs147785620 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50494331 | ACTTCATGTATAAAT[C/T]TGTTCTCATAACCTG | 11124 |
rs147798220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50577742 | TAGCCCTCAACTGGA[C/T]GAGTGTCCTTCATAG | 11124 |
rs147802724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50490069 | TGTAAGAAATATTAA[C/T]AGTTTTGCAGCTGGG | 11124 |
rs147820102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512604 | CTATATATCTGTTTT[C/T]GTACCAGTATCATGC | 11124 |
rs147827373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50892486 | TGGCCATCTTGGAAC[C/T]GCCTCCCTTCAGCTC | 11124 |
rs147835447 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885312 | CTCTCTCTCTCTCTC[A/T]CACACACACACACTC | 11124 |
rs147836993 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50560098 | CTCCACACCTGAGCT[A/G]TATTTGCCAGATCAA | 11124 |
rs147845245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50753197 | CCCAACCTCTTCCCT[A/G]GAGAACCACTAATTT | 11124 |
rs147846559 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50846844 | AGAGGAAGAAGTGAG[A/G]AGATTCACCAGGAAT | 11124 |
rs147862797 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50898523 | TATAATATGCTACCA[C/T]TTATTATTCATATAT | 11124 |
rs147864087 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50732042 | TTCTATAGCTGACAA[A/C]GATGTATTGCTAAAT | 11124 |
rs147867212 | snp | A/T | 1.65441e-05 | 0.00287607 | intron-variant | FAF1 | GRCh38.p7 | 1:50596105 | TGTTCAAAGAAAAGC[A/T]GGCAAACAGGCTTAC | 11124 |
rs147869382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50646279 | CACATTGGTAAAAAT[C/T]GGCTCACAATGTAGC | 11124 |
rs147880016 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50729482 | AGCAATCCTAGCTCA[A/G]TGCAACCTCTGCCTC | 11124 |
rs147880501 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50778316 | GCAATAAATATTCTC[C/T]ATCTGGATCTGGGTG | 11124 |
rs147886252 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641396 | ATGTTTTCATTTTAA[C/T]TTAGTTTAAAATGTT | 11124 |
rs147904047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50599968 | TCTGAAATGCTCCAA[C/T]GAGCATTTCCTTTTA | 11124 |
rs147905663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512902 | TTCACTGTCTATCTA[C/T]TGATTTGGTAAATCT | 11124 |
rs147924652 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50772526 | CACAGCCATAAAAAA[-/A]GAATGAGATCATGTC | 11124 |
rs147927246 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50911854 | CCTGGGCAACATGAC[A/G]AAACCCCATGTCTAC | 11124 |
rs147927951 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50441982 | ACCATGCCCAACGAT[A/G]AAGATCTCCCCTGGT | 11124 |
rs147947624 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50875360 | CTAAATGGGGCTAAC[A/G]TATGTATTACCCTAC | 11124 |
rs147950430 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50771832 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 11124 |
rs147964170 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50916025 | CAGCCCTCTGTTTGA[A/T]AATTCCAGCCCATGT | 11124 |
rs147964238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50869016 | TCTCCATTTGTACTT[A/G]TGGATTTGTCTATAT | 11124 |
rs147972280 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50562546 | AAATCTCTAAATAGA[A/C]AGAGTAAAGTTCTAA | 11124 |
rs147973368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50472513 | TTTTGGTTGTCCTAC[A/G]GTGCTCAGTTCAGGG | 11124 |
rs147980333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910001 | GCTCTGGTTTCTCGC[C/T]ATCTTTGTGTTTTTA | 11124 |
rs147982975 | in-del | -/ATTTTTAGT | 0.112983 | 0.209108 | intron-variant | FAF1 | GRCh38.p7 | 1:50743502 | CCAGCTAATTTTTGC[-/ATTTTTAGT]AGAGATGGGGTTTTA | 11124 |
rs147983396 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50820230 | TCACAACAATGTGAA[A/C]ATAGTTAATGTCAAG | 11124 |
rs147988908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50611709 | CAATGCTAATGTTCA[C/T]TAGGAAAACAGGAGT | 11124 |
rs148019416 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50763861 | ATTGCAATAAACTTT[G/T]AAGAAACCACCATTT | 11124 |
rs148049255 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50953468 | GGCCAGACGCAGTGG[C/T]TCACAGCGCCTGTAA | 11124 |
rs148054386 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50744157 | TAAAATTGCAATACT[C/G]TCTGCAAATTCTTAA | 11124 |
rs148072719 | snp | A/G | 0.00459238 | 0.047698 | missense | FAF1 | GRCh38.p7 | 1:50596138 | CTTCCGACTGTTCCC[A/G]GGTCTGTGCAGGTGA | 11124 |
rs148088306 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50813636 | AACTAATTTTAAAAA[-/T]TTTTTTTGTAGAGAC | 11124 |
rs148101314 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50919145 | TACCCAACAGATAGG[C/T]TTACCACTAATTCTA | 11124 |
rs148104846 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50795365 | CATTCATGGACTTTG[A/C]GAATACCATATTGAT | 11124 |
rs148107062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709916 | ACAATAATTTGATAA[C/G]TAGATATGGAGGATG | 11124 |
rs148112028 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50592153 | TGCCTCAATTTTCTC[A/G]TTAATCATATAATAT | 11124 |
rs148116869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502989 | CCACCATGTCAGGCT[A/G]ATTATTCTAATTATT | 11124 |
rs148118705 | in-del | -/GTATC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662679 | TATTAAAATGAATTT[-/GTATC]TTTTTTTTTTTTTTT | 11124 |
rs148120807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848582 | TCCATTGGAGAAAAC[C/T]GGGAGACGCTATCTT | 11124 |
rs148130323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50557113 | GGTATGGCAATCAAG[A/G]CTTTTTAATTTTTCA | 11124 |
rs148138388 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | FAF1 | GRCh38.p7 | 1:50905936 | GCTTTTGGTGTTTTA[C/G]TCATGAAGTCCTTGC | 11124 |
rs148162809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50715344 | CAGTGCTGTGTGCCT[A/G]TAATCCCAGCTACTT | 11124 |
rs148165063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625492 | CAATCAATGCTTTGG[C/T]AGTACAAGAAGAGAT | 11124 |
rs148167679 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50508610 | GAGTGACTGCCTAAT[A/G]GGTAGGGGGGTGATA | 11124 |
rs148182693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607692 | TCTCTTTCTGAAAGC[C/G]TTCTATATGACCTCC | 11124 |
rs148190411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870146 | CTCTACAGCACCGTG[A/T]AGATATTGCATTTTT | 11124 |
rs148198162 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50653378 | TGTTTTTCAGATGGA[A/G]TTTTGCTCTTATTGC | 11124 |
rs148198646 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50739496 | AAACCTGAATGTTAA[C/T]ATATAAACTCTTTAG | 11124 |
rs148201191 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50522224 | TGGTAAGAGCACTGA[C/T]TCAGTTTATCCCATA | 11124 |
rs148205917 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50443705 | AGGTTGTTGTGATTA[C/T]AGTTAAATGGAATAA | 11124 |
rs148222799 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466931 | TCTCCTCATAACAAT[A/C]TACCAAAAAATCCTA | 11124 |
rs148236865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50527949 | AATCACAGCTCACTG[C/T]AGCCTTGACCTCTTG | 11124 |
rs148250174 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50658744 | GCTGAGAGAGTCCCA[C/T]GTAAAGCATATTAGG | 11124 |
rs148259637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452465 | AGTATGGTTCTCCAG[C/T]AAGACACACAAACAC | 11124 |
rs148268349 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50787730 | TAGGGTATTTTTTTA[A/C]AGCTCTTAGATGTTT | 11124 |
rs148312703 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | FAF1 | GRCh38.p7 | 1:50884509 | TCTGGGCCACAGAGT[C/G]AGACTCTGTCTCAAA | 11124 |
rs148314761 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50958938 | CAAAGGTAGCACTCA[C/G]AGGATATTAGTTCTA | 11124 |
rs148320049 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662558 | CTTCCATGGGTAACA[G/T]GGTTATGTTGATAAT | 11124 |
rs148321476 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50749576 | GGACAGCTTGAGCTC[A/G]GAAGTTTGAGACCAA | 11124 |
rs148322079 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50630015 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 11124 |
rs148325590 | snp | C/T | 0.031825 | 0.122064 | intron-variant | FAF1 | GRCh38.p7 | 1:50546514 | GGGATTACAGGCACG[C/T]GCCACCACACCTGGC | 11124 |
rs148332364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50892712 | ACCATTTTTTAATTA[C/T]ATACTAATATCTTTC | 11124 |
rs148337945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50802007 | AATCAGTAACTTCAT[C/T]TTATAAACATTATTT | 11124 |
rs148341041 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684651 | CAAGGTACCAACACT[C/T]TGTCAGATTCACAAA | 11124 |
rs148342494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601409 | CTGGGCGTGGTGGCT[C/T]GGTGTGAGACACCTG | 11124 |
rs148350079 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50945243 | GATTGGTTTCTAGGG[C/T]CACGATGGCGTGGCC | 11124 |
rs148353275 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828259 | AAAAAAGGGTCTTTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs148370934 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50668360 | CCTCCAAAGAACAGC[C/T]CTGAGAGATACTTAA | 11124 |
rs148378190 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50551764 | CAGGCTAAGGTAGAC[A/G]ATTCATTTGTCATCA | 11124 |
rs148378561 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461010 | ACAAAGTTATGTACC[A/G]AGTGGTTGATGAAAA | 11124 |
rs148380968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930494 | TCAGTGTTCTCACTC[A/G]TACAATGGTAATAAC | 11124 |
rs148388865 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50809995 | GCGCAGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 11124 |
rs148404966 | in-del | -/A | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50826108 | ATATCAATAAATTAC[-/A]AAAATGAAAGCAAAT | 11124 |
rs148416073 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50846289 | TTTGCAAGTGACAAG[C/G]TGTCATCAGAAACAG | 11124 |
rs148418703 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50886430 | CATATGCACAATGTA[C/T]AGGTTTCTTAGATAT | 11124 |
rs148421993 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50751832 | ATTAGGGTAATGCTA[C/G]CTTCATAAAATAAAT | 11124 |
rs148423709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632764 | GGTGTCCCACACTTA[C/T]GCATTGTTTGTGGTG | 11124 |
rs148428961 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50548955 | TGGAATTGGTCTGTG[G/T]ATTAATAAATTCTAC | 11124 |
rs148432866 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50896785 | GTCAGACAATGGTGT[A/G]AGGGGCATGGAAAAT | 11124 |
rs148443132 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50604065 | AAACACTACCATGTA[A/G]GCAACCGGAGCTGGA | 11124 |
rs148450176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50946707 | AACTTTATGATTCAC[A/G]GCAATATTAGTAGTC | 11124 |
rs148456195 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50738252 | AGTTCAAGACCAGCC[C/T]GACCAACATGGAGAA | 11124 |
rs148473203 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50671927 | TCCTCCTGCCTCAGC[A/C]TCCTGAGTAGGTAGG | 11124 |
rs148473891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757554 | CTAGCTCATCCCATA[C/T]TAACATAGATCCTTC | 11124 |
rs148474775 | in-del | -/AATAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527580 | ATATTTCTCACTGAT[-/AATAG]AATAAAGAGTGATGA | 11124 |
rs148480847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464224 | GTTGCCCAGGCTGGT[C/T]TTGAACTCCTGGGCC | 11124 |
rs148486158 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50905142 | ACATGTGGTGTCTGT[C/T]TTACTGTATTTGCGA | 11124 |
rs148490107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50812644 | TGTAACTTAGTTCAG[C/T]CATTCTGGAAACCAG | 11124 |
rs148491787 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50685766 | AGTATAAAACATTAA[C/T]TCAATATGAAGCTTC | 11124 |
rs148503046 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50911003 | TCCTATTTGGCCATC[C/T]TGGAACCTCCTTTCA | 11124 |
rs148507691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822637 | CTATTCAATGAAATG[G/T]GGAGAGGAAAGGAAG | 11124 |
rs148516149 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50582115 | ATATATATCACTACA[C/T]AGAATAATCATTTTG | 11124 |
rs148531719 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50517497 | ATACTAGGTACCAGT[G/T]CATGTTAATAGCAGG | 11124 |
rs148544469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50651635 | TTAAACCATTCTAAG[C/T]ATTAAGTTATGGCAC | 11124 |
rs148562845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707964 | AGCTGCGTGCGCCAC[C/G]ACGCCCAGTTAATTT | 11124 |
rs148564319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618918 | CATACCACCATGCCC[A/G]GCTGATTTTTGTATT | 11124 |
rs148569163 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50500509 | TACATCACACTATAT[A/G]CAAAATTTAACTGAA | 11124 |
rs148575181 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50924361 | AATCAATTTAATCAA[A/G]AAGGTAAAAGACCTC | 11124 |
rs148578588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50838184 | TTTTATGGGCTGAAC[C/T]ATCTGGGGTAAAGCC | 11124 |
rs148587996 | in-del | -/AAGAAATAATGAAACAGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713232 | GATGAGTGTTAACCA[-/AAGAAATAATGAAACAGT]AAGAAATAATGAAAC | 11124 |
rs148588882 | snp | A/G | 9.96049e-05 | 0.00705638 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50705834 | GTTGTACTCCCGCTG[A/G]ACTTCTCGGTGGGTG | 11124 |
rs148621239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50458487 | ATATTCATTGTCATC[A/G]CTCCCCACCATTCCA | 11124 |
rs148629086 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50711575 | CCCAGGTTCAAGCGA[A/T]TCTCCTGCCTCGGCC | 11124 |
rs148630130 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50797706 | AACAAACAACAACAA[A/C]AAAAGATACTAATGG | 11124 |
rs148635929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50592855 | AGGCACGAGAATTGC[C/T]TGAACCCGTGGGGAG | 11124 |
rs148647654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852393 | TCAAGTATTCATTAG[G/T]CAATTACTATATGTC | 11124 |
rs148648619 | snp | A/G | 6.59076e-05 | 0.00574016 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50490591 | ATTATGCCCCACCTC[A/G]CGTTCCTCTTCTTGT | 11124 |
rs148658685 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50907257 | GGTGTATAAACTTTT[C/T]GATGTGCTGCTGCAT | 11124 |
rs148667521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777288 | GCCAAACATGGTGGC[A/G]TGCGCCTGTAGTCCC | 11124 |
rs148680930 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50719144 | TTTAAATTGTCTCAG[G/T]AACAGCATAAAAATA | 11124 |
rs148690535 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50511931 | GACTTTTTAATGATC[A/G]CCATTCTAACTGGCG | 11124 |
rs148694545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50859072 | TTCAATAAAACCCAA[C/T]ATCCCTTTACAAGGA | 11124 |
rs148698031 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50760593 | TGAATGACTACTGGG[C/T]ACCTAACGAAATGAA | 11124 |
rs148706030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523296 | AGGAGTGGAATACCT[A/G]GTTCAAATGGTTACT | 11124 |
rs148712777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952038 | AGAGGAGCTCATATG[C/T]AAAGTTTCAAAGACC | 11124 |
rs148716590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874794 | TTTTTTTTGGAGACA[A/G]GGTCTCACTCTGTCA | 11124 |
rs148720470 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50741301 | AAGATGTAAAGAGCT[G/T]GAGCCTATTAAAAGA | 11124 |
rs148722322 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50655115 | AGTGGGATTAGAGGC[A/G]GCCGCCAAGTGATTC | 11124 |
rs148724004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50539023 | TTTACACCAACCCTT[A/G]GAGTGCATTACTAAC | 11124 |
rs148743632 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468686 | GGCTGGTGTTGAACT[C/T]CTGACCTCGTGATCC | 11124 |
rs148776882 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50577474 | AGTTTGCAGTGAGCC[A/G]AGATGGCGCCACTGC | 11124 |
rs148779349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50453995 | TGTCCTCTGAGATTC[C/T]TTGTCTGTTAAACAA | 11124 |
rs148780993 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50922076 | AAGGTTGAGGCAGGA[A/G]AATTGCTTAGAACCC | 11124 |
rs148785408 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50887775 | ATGCTGTTTTGGTTA[C/T]TGTAGCTTTGCAGTA | 11124 |
rs148790293 | snp | C/G/T | 0.00279258 | 0.0372817 | intron-variant | FAF1 | GRCh38.p7 | 1:50791428 | TGCTAGATGGTTTCC[C/G/T]GTTAGATTCTACCAA | 11124 |
rs148820480 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50878102 | TTTTAATAAAACTAA[C/T]CTTCTCTTTGTTCTT | 11124 |
rs148826540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657343 | AAGTTAATTATGGCA[C/T]TATTATCCTACTGTA | 11124 |
rs148860929 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50611679 | AAAGTCTGAGAAATA[C/T]GTCCACATCATAATC | 11124 |
rs148878546 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50662046 | GCTTTTTTTTTCTTC[C/T]CCCTTCCCCCAGGGC | 11124 |
rs148880054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50546404 | AGAGTCTCACTCTGT[C/T]GTCTAGGCTGGAGTG | 11124 |
rs148881741 | in-del | -/GAATC | 0.111576 | 0.20818 | intron-variant | FAF1 | GRCh38.p7 | 1:50879284 | AATGAATGAATGAAT[-/GAATC]AGATTAATGTAATTC | 11124 |
rs148884420 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50455335 | AATGCATTTGAATAA[C/T]CTTAGGTGACTTAGC | 11124 |
rs148890459 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50793657 | ACTAATTTGTAAGCA[C/T]TGGGACGTGCATTTT | 11124 |
rs148911227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748134 | GAGAAATGAGACTTA[A/T]ATTAAACTTGAAGTA | 11124 |
rs148942124 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50753934 | AGCTAATTTTTGTAT[C/T]TTTGGCAGAGACGGG | 11124 |
rs148951333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50549604 | ACAAGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 11124 |
rs148955613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50899218 | TGAAGATGTTTGATT[C/T]AGGACTTTTCACATG | 11124 |
rs148964762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766620 | GATGCTGGACCAAAG[A/G]GGTAGGAAGCTGGGG | 11124 |
rs148966927 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50683483 | AGTGAGCCGAAATCG[C/T]GCCACTGCACTCCAG | 11124 |
rs148970007 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50481997 | TAATAATTATTTTCC[C/T]ATTTTAAAATTAAGG | 11124 |
rs148979307 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50739335 | GTGTACATGTGTACA[C/T]GTACATGCATATACA | 11124 |
rs149003515 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556987 | ACATAGCTTTCCTAA[C/T]AGCCACATAATAAAA | 11124 |
rs149007343 | snp | A/T | 0.112631 | 0.208878 | intron-variant | FAF1 | GRCh38.p7 | 1:50905879 | CAGAAGCTCTTTAGT[A/T]TAATTAGATCCCGTT | 11124 |
rs149012948 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50814549 | ATTCAAAAAACAAGC[C/T]AATTATAGATATATT | 11124 |
rs149022319 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50443441 | GCCTACTATATGCCA[G/T]ACAACATATCCATAC | 11124 |
rs149029885 | in-del | -/A | 0.295854 | 0.245759 | intron-variant | FAF1 | GRCh38.p7 | 1:50613790 | AAAATCTTTTATATT[-/A]AAAAAAACAAACAAA | 11124 |
rs149031495 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50702205 | TGGGTTTTGGATTTG[C/T]TGAAAGCAAATCAAT | 11124 |
rs149031709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50787422 | TTGATGAAGGGAGTC[C/T]GTCCCTTTTGCCCTT | 11124 |
rs149036913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50584557 | TAATGAAGAATGCCT[A/G]CTCTCTATTATCTTA | 11124 |
rs149038573 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50494924 | CTGTCCTGAGTATTA[C/T]GATGAGTTGTTAAGA | 11124 |
rs149044067 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50927486 | ACTTGGGAGGCTGAG[G/T]TTGCAGTGAGCCAAG | 11124 |
rs149066436 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672033 | CTTTTTTTTTTTTTT[-/T]ATTATTTATTTACTT | 11124 |
rs149067372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652593 | CAACTATTTTTGCTT[C/T]AAACTTTTTATTATG | 11124 |
rs149072501 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50568823 | GGCTTATGGAAGCAC[A/T]CATATAACATGAAGA | 11124 |
rs149083180 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50709575 | TGCCCCTGGTCATCA[A/G]GCTACAAAGAGGTGG | 11124 |
rs149091970 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50502925 | CCTGGGCTCAAGTGA[G/T]TTTTTTTTCCTGCCT | 11124 |
rs149096276 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50848125 | ATGCCAGACAAAAAC[G/T]TAAACTTATACCAAA | 11124 |
rs149102007 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50840448 | AAAAGATTTTAATAG[A/T]TACTTCACCAAAGGA | 11124 |
rs149106007 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50628912 | GGCCATTCTTTGGGG[C/G]TTCAAATCCCACTGC | 11124 |
rs149117642 | snp | A/G | 6.59326e-05 | 0.00574125 | missense | FAF1 | GRCh38.p7 | 1:50744703 | TCTTCCACATCTCCC[A/G]TCTTCCAGCCTTTTA | 11124 |
rs149124806 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733619 | AGTTCTCTCTCTCTC[-/CT]CTCTCTCTCTGCCAT | 11124 |
rs149126847 | in-del | -/TT | 0.11228 | 0.208646 | intron-variant | FAF1 | GRCh38.p7 | 1:50661865 | GGCCTTCTTTTCCTC[-/TT]GTTTTTAAAAGTATT | 11124 |
rs149143599 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460942 | ACTGGTGTGAGCCAC[A/T]GCACGTGGCCTAAGT | 11124 |
rs149144829 | in-del | -/GCTGTTATG | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50833004 | CAATCACTCTACCAT[-/GCTGTTATG]GCCTTTTTTTCCCCC | 11124 |
rs149154651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50801122 | AAAACCATTCCACTT[A/G]TTAACACTGGATACT | 11124 |
rs149165645 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938207 | AATTGTGGAAAATAA[A/C]TAAAAGCCAGGACTC | 11124 |
rs149185104 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50882372 | GCCAAGGCGGGTGGA[A/T]TACTTGAGGTCAGGA | 11124 |
rs149190801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50780344 | CAGAAGGAAATATAG[C/T]TGCCAAAGGGTTTTA | 11124 |
rs149212824 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50601175 | ACAATAAACAAAGCA[C/T]ATAGTATTTTCTTTG | 11124 |
rs149213426 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50513627 | TACCATTAACTAAGT[A/C]AGTATTTGCAAAGGA | 11124 |
rs149219997 | in-del | -/AAGGAAAGGAAAGGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917626 | AAAAGGGAAAGGAAA[-/AAGGAAAGGAAAGGA]AAGGAAAGGAAAGGA | 11124 |
rs149224527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860807 | TCGCAGCACTATTCA[C/T]AATAGCAAAGACATG | 11124 |
rs149230723 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50647769 | AGTTACGGAGACTGA[C/G]ATCCATAGACATTAA | 11124 |
rs149259671 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50680757 | GTGACCTAAGGGATC[A/G]TCTAGTCAAAACACT | 11124 |
rs149267183 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471314 | TTTAGCTTGGTGCTT[A/G]GCATAATAAAAGTGG | 11124 |
rs149268823 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50941670 | TTTGGATGCATTTGA[A/G]TTTGCTTTATAAAAG | 11124 |
rs149276432 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820082 | AGGTACTTAAAGTAG[A/C/T]TGAATTCACAGACAC | 11124 |
rs149288352 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50883991 | TTAGCCAGGCATGGT[A/G]GTGCACACCTCTAAT | 11124 |
rs149304656 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50923020 | AATTGGAAAACCTAG[A/G]GTAAATGGATAAATT | 11124 |
rs149304908 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457652 | CAGCACTTTGGGAGT[C/T]TGAGGCAGGCAGACT | 11124 |
rs149314694 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50603578 | ACTGCCAACCAAAGC[A/G]CAACTCTAAAAAGCT | 11124 |
rs149320604 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50478976 | ACAACTCTGATCAAG[C/T]ATCTCAGAAGCATAC | 11124 |
rs149322214 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50946313 | GATTGGTGAAAAATA[A/T]CCTCCCCACCCAAAG | 11124 |
rs149327488 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50737934 | ATCTAAAAATAAACA[C/T]AGTTCTGGAATAATA | 11124 |
rs149333519 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50650373 | AGCACTTTGGGAGGC[C/T]GAGGTGAGGATCACT | 11124 |
rs149336966 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50531838 | CTTGGGTTTATTTAA[C/G]AAAAGTTTTAAACAT | 11124 |
rs149338408 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50954321 | TTTTTCTTTCTTCAC[C/T]TGAGTACAGCTATGA | 11124 |
rs149345317 | snp | A/C/G/T | 0.00438476 | 0.0466401 | intron-variant | FAF1 | GRCh38.p7 | 1:50746591 | ACAGGCATGAGCCAC[A/C/G/T]GAGCCCGGCCAATGA | 11124 |
rs149354633 | in-del | -/TCTG | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50608955 | GTATGTGTATCTGAA[-/TCTG]TCTATCAACCAATAT | 11124 |
rs149383827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612948 | CATTGTATCTGTGTT[C/T]AGGTGACTCTAAGGT | 11124 |
rs149388917 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50492566 | TATTCAGAAGTATAG[C/T]CAATATACATATACT | 11124 |
rs149397656 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50751344 | TTTGTTTGATTGTTT[C/G]TTTGTTTTGAGATGG | 11124 |
rs149407241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50548676 | GATTCTAAACTTACT[A/G]TCTAATTTTTAGCAA | 11124 |
rs149407485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457067 | ATAGGTTTTTTTCCC[C/G]TAGTTTTCACAGTAA | 11124 |
rs149414735 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50803772 | CTTTCCTTTCCCAAA[A/C]CCTTAGATTATTAAA | 11124 |
rs149417808 | in-del | -/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938037 | AAGAATTAAAGACAC[-/TG]TTTTTTTATTAGGCA | 11124 |
rs149420347 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50758830 | TCTGATAGAAGTCTG[C/T]ATTTTTTATTATTAT | 11124 |
rs149420376 | in-del | -/ATATAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554365 | GATTAAATGAGGTAA[-/ATATAT]ATATATATATATATA | 11124 |
rs149471119 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50724922 | TAAGGCAGGTCTACT[G/T]CATCAGTCCATCAGG | 11124 |
rs149479915 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50519642 | AATGAGAAGTATGTA[C/T]GGCTATTGTTAAAGT | 11124 |
rs149484175 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | FAF1 | GRCh38.p7 | 1:50869752 | GATGTACTTTTAGAT[C/T]CTTTATAAAATCCAA | 11124 |
rs149486938 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50902588 | AAAGTCACACAAACT[A/C]TATGCAGTTGTCTCT | 11124 |
rs149487599 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50769867 | ACCAGCCTGGCCAAT[A/G]TGGTGAAACCCCATC | 11124 |
rs149497464 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50950684 | GACACTATGTGCATT[C/G/T]CAAGGCTTCTGAACA | 11124 |
rs149498265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486758 | CACAGCACCTGATTT[A/G]ATAATTTGCACACAG | 11124 |
rs149501185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50917909 | CCATACTCAAAACAG[C/T]GCATGCTGTATGACT | 11124 |
rs149505472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50832215 | CCTCTACTCCAGTCC[A/G]CAGAAAAACTGTTGT | 11124 |
rs149510508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50620514 | CCTGAATCTCAATGC[A/G]CTTCGTTGACATCCA | 11124 |
rs149517258 | snp | A/G | 1.65482e-05 | 0.00287643 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475626 | GCTCACAGGCTCAGC[A/G]TTTTCTTCCTTTGGC | 11124 |
rs149528388 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50645026 | TTCTTTTCTTTTAAA[C/T]CCAAACTTTCTTCTA | 11124 |
rs149529340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50558671 | TGGAATGGCTTGCCA[A/G]TAATATCACCTTTGT | 11124 |
rs149533827 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50906826 | CATGTCATCTGCAAA[C/T]AGGGACAATCTGACT | 11124 |
rs149536787 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50818196 | ACCACAAAAAATTCC[A/G]TCTTAAACACACTAA | 11124 |
rs149540818 | in-del | -/ATA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931908 | TAATAATAATAATAA[-/ATA]TAATAATAATAATAA | 11124 |
rs149542668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775925 | AAACAGAGAAAGTAT[A/G]TAACATGATTCTCTG | 11124 |
rs149547019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50575358 | ACTAACAAATATACT[A/G]TTTAGTAGAAATATC | 11124 |
rs149558859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50791152 | AAGTAATCTTGTACA[A/G]AAAAACATGGGAACC | 11124 |
rs149560211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667965 | TGCTTTGCTGTTTTC[C/T]GTTGCCCATCCAGGC | 11124 |
rs149561720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50706166 | GTCATAGGCTAATTC[A/G]TAATATCTGCATACG | 11124 |
rs149562794 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50588053 | GCACTTTCAGAGGCC[A/G]AGGCAGGCGGATCAC | 11124 |
rs149567575 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | FAF1 | GRCh38.p7 | 1:50954905 | TCCCACCTACTCAGG[A/T]AGCTGAGGTGAGAGG | 11124 |
rs149570311 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50929445 | CTTTGGTTGATAAAA[C/T]TGTATTCAGATCCCT | 11124 |
rs149574637 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50843216 | TGTGTCACATATGTG[A/G]TAAGAGGGTTTGCCT | 11124 |
rs149582773 | in-del | -/AAATACAGTGG | 0.00141909 | 0.0266013 | intron-variant | FAF1 | GRCh38.p7 | 1:50490540 | AACAGCTTCAGTATC[-/AAATACAGTGG]AAATACAACCCAGCT | 11124 |
rs149597329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50654767 | GTTTTTGCCTTGAAC[A/G]TTTCATTAGTAGTAT | 11124 |
rs149598750 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50537998 | TATTGCCCTTTGAAA[C/G]GATCTTTTATCTATA | 11124 |
rs149616800 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50504928 | ACTTCAGAATAACTG[A/C]ATCAGAAATATGAAC | 11124 |
rs149627447 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50852223 | TTATTCCTTGGGTGT[A/C]TGGGTTGTCCCGCTC | 11124 |
rs149652558 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50453414 | GAGTTTAGTCCCTAA[C/G]GACATACAAAAGACT | 11124 |
rs149656943 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50793016 | CTTTTTTTTTATGGC[A/G]GAGTCTCGAACTGAG | 11124 |
rs149657949 | in-del | -/ACTC | 0.118933 | 0.212888 | intron-variant | FAF1 | GRCh38.p7 | 1:50674369 | GCCAAAGAAATTGTT[-/ACTC]ACACTATTCACTTAC | 11124 |
rs149670054 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50931558 | TCAGATCTCAAGAGA[C/T]TTATTCACTATCACA | 11124 |
rs149670739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463660 | GACAGAATACTTTCT[G/T]AAATGTCTGCACAAG | 11124 |
rs149679418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50811969 | GCAATGGGGAAAGGA[C/G]TCCCTGTTCAATAAA | 11124 |
rs149689584 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50555247 | CACACCAGGACCCTG[-/AC]ACACACACACACACA | 11124 |
rs149702358 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50753758 | TGTCATTATCTGTTC[-/TT]TTTTTTTTTTTTTTT | 11124 |
rs149703310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50450281 | ATCTAATTAAATGGT[C/T]CCAACAATTCTATGA | 11124 |
rs149716056 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50594500 | TCCTTATAACCATGG[A/T]CAGAGTTGGGCATGA | 11124 |
rs149720677 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50506938 | CCTGCCATTACTGCC[A/T]TTACCTCTATCTTAA | 11124 |
rs149727768 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50853862 | CAAACTTATGAAGAT[C/G]TATTAAAAATCTGTA | 11124 |
rs149734277 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | FAF1 | GRCh38.p7 | 1:50722478 | ATGGTGAAACTCGGT[C/G]TCTACTAAAAATACA | 11124 |
rs149764109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880832 | CATGAGTTGTTCAGT[C/T]GTAGAGTTACCATCA | 11124 |
rs149787062 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50682378 | TGTGGTAGCACGCAC[C/T]TGCAGTCATAGCTAC | 11124 |
rs149804208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50731960 | ATTCTTTGATACTGG[C/T]TTTGTGTTCTACTAC | 11124 |
rs149818391 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50886288 | TTGATGAAATCCCTC[C/T]GCTTTTCTTTGGGAA | 11124 |
rs149824031 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50664122 | CCTGCCTCAGCCTCC[C/T]GAGAAGCTGGGATTA | 11124 |
rs149834422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50927177 | GATGAGTGGTGGTGA[C/T]GCCACATAACAATGT | 11124 |
rs149845815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50947986 | CCAGACAGTTGTTTC[C/T]CCAACAGAGCTGACA | 11124 |
rs149859299 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | FAF1 | GRCh38.p7 | 1:50618555 | GGCATGAGCCACCGC[A/G]CCCGGCCACCTAAAT | 11124 |
rs149860746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534665 | GTTTAAAAGTGTCTA[C/T]TTACTGCCATAACAC | 11124 |
rs149862204 | in-del | -/ATTT | 0.0368353 | 0.130617 | intron-variant | FAF1 | GRCh38.p7 | 1:50599593 | TTATTAAGTAATTTA[-/ATTT]ATTTATTAAGTAAAT | 11124 |
rs149870180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50839865 | AAATTTAATCAACTT[C/T]CAAACATACAAAGCC | 11124 |
rs149875420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50627724 | TGGGATACTTTAAAA[C/T]GTTTTCTTTCTTAAT | 11124 |
rs149879764 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50544829 | AGACTCAAAAGAGGT[A/G]AAGGAGGAAATGAAA | 11124 |
rs149888453 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | FAF1 | GRCh38.p7 | 1:50760498 | CTGTCTCTCAGACCA[C/T]GGTGCAATCAAACTA | 11124 |
rs149915777 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50494715 | GCTGTACACTCCCAG[A/G]GGTAAAAGACTCTAT | 11124 |
rs149939282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807589 | AATTACAATTCAACA[C/T]GGGATTTGGGTGGGG | 11124 |
rs149940513 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50898974 | TCTGCCTTCTGCAGA[C/T]TCCAATTACACGTTT | 11124 |
rs149976310 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50915285 | TGAGGCACGAGAATC[A/G]CTTGAACCTGGGAGG | 11124 |
rs149999649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50639234 | TCTGGGTTTTGTCTA[A/C]TATAAATAAAGCTCC | 11124 |
rs150001571 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50521898 | GGCTCTGAACAGGTG[C/T]GCTGAATTGTAACGC | 11124 |
rs150011115 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FAF1 | GRCh38.p7 | 1:50771564 | AAGTCAAAACCACAA[C/T]GAGATACCATGTTAT | 11124 |
rs150012473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50874235 | TCTACCAGACCATTT[A/G]AAAGTCTATTGTTTA | 11124 |
rs150018604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50572746 | AAACTCTTTTCTAGA[C/T]GGGAGTAGTGAGGAA | 11124 |
rs150022925 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50921568 | GGAGTTCGAGACCAG[C/T]CTGGGTAACATGGTG | 11124 |
rs150030844 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | FAF1 | GRCh38.p7 | 1:50711461 | AATGTTATCCACACT[G/T]ACTTTTTTTTTTTTT | 11124 |
rs150035565 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50622585 | CAGGAATCTAATATT[A/G]CTTGAAATTTACCTG | 11124 |
rs150051139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50647003 | TGTGTGAGCCACCAC[A/G]CCCAGCTAATTTTTT | 11124 |
rs150052314 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733792 | TATGGTACTTTGTTA[-/T]TAGCAGCCCTAGCAA | 11124 |
rs150062413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779012 | TTTATCAATTAAGTT[C/T]ATGTCACATTCTAAA | 11124 |
rs150076617 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50916850 | ATCCTATCCATTCAT[A/G]GATTAGAAGCAAAAG | 11124 |
rs150101717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50611334 | TAGACAAGGTAGATA[C/T]TAACACAAAAAGAAA | 11124 |
rs150105648 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50526252 | GCCTACCTTGGCCTG[A/C]TCATGGTGGCATGAG | 11124 |
rs150111962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50774776 | CAATATACAATAATC[C/T]CTACCCTCAAAGAGA | 11124 |
rs150125839 | in-del | -/ATAAGAG | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50581620 | GTGTTAAGTGTAACA[-/ATAAGAG]ATAAGCAGAGGGTTT | 11124 |
rs150135599 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | FAF1 | GRCh38.p7 | 1:50712530 | GCGTGGTGGCACACG[A/C]CTCTAATCCCAGCTA | 11124 |
rs150141489 | snp | A/T | 1.66435e-05 | 0.0028847 | missense | FAF1 | GRCh38.p7 | 1:50596216 | ATTCAGCAAGACACA[A/T]CTGCAAAAAGTAGAA | 11124 |
rs150155748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50531541 | GTAATACTTGTTTTC[C/T]TCCTCACCCACTCTT | 11124 |
rs150163883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50781583 | ACACCCCATTTTCAA[G/T]AATGAATAGAAATAT | 11124 |
rs150172172 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50661924 | TTGTTTTACTAAGAT[A/G]CAAGTTAAAACCCTC | 11124 |
rs150172412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50579828 | TACTCAAATATAACT[C/T]GTGATCCTTGAGTGG | 11124 |
rs150178110 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50455076 | ACAGCAGGCAGACTC[C/T]GTTGGTGATACCATC | 11124 |
rs150181510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50795935 | CTGGAGCCCAGGAGA[C/T]TTTCTGGGGCATGTC | 11124 |
rs150183244 | snp | G/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50890419 | ATGATGTTAGCTGGT[G/T]ATTTTGCTCGTTAGT | 11124 |
rs150188588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50592258 | AACTGATGCTTTTAA[C/T]ATTACATTAAAACTT | 11124 |
rs150193293 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465741 | TATTTTATATGGGTT[G/T]GTCAGCAAAGGCCTC | 11124 |
rs150198978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50933841 | AGTTTTACATGGCAA[C/T]GGCAAGAGAAAAATG | 11124 |
rs150200472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50813690 | CTTGTCTCAAATTCC[C/T]AGGCTCAAGTGACTC | 11124 |
rs150205043 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50723979 | GTCTCGAACTCCTGA[A/C]CTCAGGTGATCCACC | 11124 |
rs150228639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452743 | AGCCTCAGAGTTTCA[C/G]TAGTAGGCATGGATT | 11124 |
rs150241546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50597496 | TGAAATATGAGGGTA[C/G]CTACAAAAGCAGTAT | 11124 |
rs150245360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941536 | CTAATTTTTCAAGTT[C/T]TTTGTAGAGACAAGA | 11124 |
rs150246222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470690 | ATTCACTTAATATAA[C/T]GCTTACCACAACCCT | 11124 |
rs150268789 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50868852 | TGTTTCATATGCATA[C/T]AAATGTGTATTCTAT | 11124 |
rs150312854 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50568695 | AATGTCACAGATAGT[A/T]AGTAACTAATACAAC | 11124 |
rs150314222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50475739 | ACTATGGAGAGTGGG[C/G]AGGAAGACACCAGAA | 11124 |
rs150314253 | in-del | -/AAG | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50568355 | TGGGATTCTGAACAA[-/AAG]AAGGAAACTTACAGA | 11124 |
rs150317602 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50912122 | CAATGGTGACAACAA[C/T]ATCATTTCAAAAATA | 11124 |
rs150319209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50945328 | AACAGGAGTGAGGCA[C/T]CACTGATAGGAAGCT | 11124 |
rs150324990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50700646 | AATTTCTCTTAACCC[A/G]GGCATTTCAAAACTA | 11124 |
rs150339174 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50887108 | CTGATTGTGGTTTTG[A/G]TTTGCATTTCTCTGA | 11124 |
rs150341520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753646 | TCTTCAACTCTAGTT[C/G]TTCAACTGGGTCATT | 11124 |
rs150367789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486702 | TTAGACAGTAAGCTC[C/T]TTGAGGGCTGGACTA | 11124 |
rs150375103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50831924 | TCGTCAGATGAGCAG[G/T]AGCAATAGAGTTTCA | 11124 |
rs150378657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50739990 | ACATTAAGAAATACA[C/T]TGTATACCTTTACAT | 11124 |
rs150379803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619588 | TTGTAGGGTTTGTGC[A/T]CACAGGCCTGCTGCT | 11124 |
rs150384516 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50537030 | TGCCCAGGTCTCAAG[A/T]GATCCTCCCACCTCA | 11124 |
rs150396308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50631472 | TATCACAGTGCTTGT[A/G]TTTAAGTTACCCTTA | 11124 |
rs150401714 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50513148 | GCTGGAAGGAAAAAT[C/T]AGCAATGACTTAGAA | 11124 |
rs150407152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894523 | GCTGTTACTTAAGGC[A/G]CAAGAAAAACTTATC | 11124 |
rs150435872 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50588018 | TCAGCCAGGCATGGT[A/G]GCTCATGCCTGTAAT | 11124 |
rs150436159 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | FAF1 | GRCh38.p7 | 1:50497764 | CATCTTGGCCAGGCT[A/G]GTCTTGAACTCCTGG | 11124 |
rs150452107 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637706 | GTGTGTGTGTGTGTG[C/T]GTGTGTGCGTGTGCA | 11124 |
rs150461445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50901177 | CCTCTTAAAAAATAT[A/G]ATCCTGCTTGGAATG | 11124 |
rs150463444 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50768859 | AATTAACAATCTAAC[A/G]TCACACATCACACCT | 11124 |
rs150468672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684774 | CTGCTACAATATAGA[A/T]AGAACGTGATATAGA | 11124 |
rs150482793 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | FAF1 | GRCh38.p7 | 1:50909242 | TTTCTGCCCAGAGAT[C/T]CGCTGTTAGTCTGAT | 11124 |
rs150500578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50632872 | CTCCTCTATGATCTT[C/T]CCAGGTAAAATTCTA | 11124 |
rs150507188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50515797 | CTCCCTCCTCACTTC[C/T]GTCTATAAACAACCC | 11124 |
rs150515189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863180 | CTGTCAGACCACAGT[A/G]GAATAAAATTGGAAA | 11124 |
rs150518818 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50764547 | ATTCCCTTTTTCATG[A/G]ACTGTTGTATAGAAA | 11124 |
rs150522672 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50648870 | GGCGGAGGTTGCGGT[A/G]AGCCAAGATCGTGCC | 11124 |
rs150538475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50590256 | GCTTTGGGCACTACA[A/G]TATTACGCCTTCCAA | 11124 |
rs150548731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931299 | ATCTGCATTGTTTAT[A/C]CTTTCTTATTGTTAT | 11124 |
rs150569432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685952 | CATGATAATTTCCCC[A/T]TTGAGAATATGCTTT | 11124 |
rs150576651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50563203 | TTTACTATTACCTAT[A/C]TGTTTTTAGCTCTTT | 11124 |
rs150581209 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50497373 | AACATATAAAACCTG[-/A]AAAAATTCATCAATA | 11124 |
rs150584036 | in-del | -/AC | 0.332337 | 0.236052 | intron-variant | FAF1 | GRCh38.p7 | 1:50601733 | TATATATATTCATAT[-/AC]ACACACATATATTCA | 11124 |
rs150622931 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573817 | TCAGAGGGTTAAAAA[-/C]AAAAAAAAAAAAAAC | 11124 |
rs150629395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528611 | CATCTTCTATACTGG[C/T]ACTGGAGTTCCTTGA | 11124 |
rs150636819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880196 | TCATGAAGAATTAAA[C/T]TGATGTCAAGCAATA | 11124 |
rs150639361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50745510 | GGAGGTGACTGGATC[A/G]TAGGGGGCTGATTTC | 11124 |
rs150641042 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50659281 | GAAGAAGGGGAAAAG[A/G]GAAAAGGAGGAAAGA | 11124 |
rs150654631 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50803541 | AAGGCCTGTCTGGCA[C/T]AGTGTCTGCACAATA | 11124 |
rs150660058 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50716471 | TGGACTTCCTGGGTC[A/G]AGTGGGGACTTGGAG | 11124 |
rs150663985 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50510400 | AGGACCTGGGGCAAA[C/T]CAGCTGTCACTAAAT | 11124 |
rs150671353 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50857753 | AGTATTCATAATAAC[G/T]TAATACTGAGCTAAA | 11124 |
rs150683021 | snp | G/T | 0.0209421 | 0.100162 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441200 | GAGGGTGAAGTGCAG[G/T]GGGTAGGGGAGGGTG | 11124 |
rs150687277 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50784321 | AAAACTTAGAACTAA[C/T]AAATAATACAAAATT | 11124 |
rs150695399 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | FAF1 | GRCh38.p7 | 1:50663605 | AGACAGGGTTTCACC[A/G]TATTGGCCAGGCTGG | 11124 |
rs150697495 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50582882 | ATTCTTCTTGGCCTA[C/T]ACTGATATACTAAAA | 11124 |
rs150699663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456773 | AAAGAATTTAGAACA[C/T]TGAAATTCAGAACAG | 11124 |
rs150704581 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50925840 | CAGATATGGAGTCAG[A/C]CTAAATGTCCATCAA | 11124 |
rs150709959 | in-del | -/ACAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50796213 | GCAGCAAACACACAA[-/ACAC]ACACACACACACCCC | 11124 |
rs150711986 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50676948 | ATTCCAACTGTGATA[C/T]ACATGAAAAAGGGCA | 11124 |
rs150716305 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467477 | TGCCACCATGCCTGG[C/T]TAATTTTTTGTATTT | 11124 |
rs150722193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50817143 | TTTGTTCTTTTTGCT[C/T]AGGATGGCTTTGGCT | 11124 |
rs150726575 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739481 | AAAATGAACTAGCAT[A/C]AACCTGAATGTTAAT | 11124 |
rs150728465 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50726024 | CTTTGGGAGGCCAAG[A/G]AAGGTGGATCACTAG | 11124 |
rs150730595 | in-del | -/TATTT | 0.452965 | 0.145963 | intron-variant | FAF1 | GRCh38.p7 | 1:50674860 | CCTGTCACCTTGTAC[-/TATTT]TATTTTATTTTATTT | 11124 |
rs150730880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50607830 | GTTCCTAAGGGGAGA[C/T]CCAGAATCCCAGGTG | 11124 |
rs150750153 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50544792 | CAGGGAAAGTCTCAA[A/T]GAAACGCTGACATTT | 11124 |
rs150780014 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50731658 | CAGGCATGAGCCACC[A/G]CGCCCGGCCTCAAAA | 11124 |
rs150784621 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50612241 | CAGTCTAGGATCTTA[A/T]CAAAACAAGCCCTTT | 11124 |
rs150785140 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50620370 | TTCATACTTGTATTG[G/T]ATTATGAAATTCTTG | 11124 |
rs150794396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50950253 | ACAACAGCTACAGCC[A/G]GTCTACCTAAGTACA | 11124 |
rs150840771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50479831 | CCAATGGACCAATGT[A/G]GAAAACAATGAAGAG | 11124 |
rs150842832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50445857 | TTAGCTTAATCATTT[A/G]GCAAATTGGCTTTGT | 11124 |
rs150847825 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50914627 | TGTATCAATCACTGC[A/G]CATTTAATTATATTT | 11124 |
rs150853283 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50616970 | ACAGGCATGAGCTAC[C/T]GCACTCAGGCTGTAC | 11124 |
rs150853437 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50705276 | AAAATACTGACACTA[C/T]AAATAGACTCTTCTC | 11124 |
rs150863845 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50959387 | CACCACACGCTCCAC[A/G]CTCACACTCCATACA | 11124 |
rs150868446 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50669404 | GGAGAGACACTGTCA[C/T]AGACTGTGTTGTCTT | 11124 |
rs150882335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810570 | ACATGGCACTGGAAG[C/T]CCTATCCAGAGCAAT | 11124 |
rs150891463 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50488576 | CTAAAAGGATAGTGA[A/C]TAATTTCTCCCTTAT | 11124 |
rs150899246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50833521 | TGTTTAGGGGTTTTA[C/T]GGAGGTTTCATTACA | 11124 |
rs150904469 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50741884 | CCAATAAGATATACA[A/C]GTACAAAAGTCAATT | 11124 |
rs150907675 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50622477 | TGATTTGGTCTCTCT[C/T]GGTAGAAGTGGCACT | 11124 |
rs150908931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50539323 | TTATGTCCTAATTGA[C/T]AGATTATACAATTTA | 11124 |
rs150912696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50504518 | ACACAGTCAAGAGTA[C/T]CTAATATGCATCTAC | 11124 |
rs150915809 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50887847 | TTTGGCTTAGGATTG[A/T]CTTGGCAAGGCAGGC | 11124 |
rs150940229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579342 | GGCTTTTAAAAATAT[C/T]TATACCTATTTTGGG | 11124 |
rs150945102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447712 | ATCTCATCTTACCTC[C/T]TACGCCAATGTCAAG | 11124 |
rs150949449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916576 | CTCTAAACGTAGAAA[C/T]AAAGATCTTCAAACT | 11124 |
rs150951014 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50792458 | CTGAGAAGGCTAGCC[C/T]CCACTTCTGTGAAAG | 11124 |
rs150953606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50829774 | TGTAACTGAGTTGCC[A/C]ATTATTGACAAATCA | 11124 |
rs150957494 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50708099 | AGGTGTGAGCCACAG[C/T]GCCCGGCCCGCCCCT | 11124 |
rs150968910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846573 | AAAAAGGAGCAATAG[C/T]GAGGAACTTGGAAAA | 11124 |
rs150972474 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50758367 | CACAACATACATTTT[A/T]AACTCAACAAAGACT | 11124 |
rs150974162 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50639048 | AGCTTTGGTTTTTCC[A/G]CATTTCATAAATGTG | 11124 |
rs150978570 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50555262 | ACACACACACACACA[C/G]ACCCCAGGACTCTGA | 11124 |
rs151009110 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50712395 | GCTTGGTAGCTCACA[C/T]CTGTAATCCTAACAC | 11124 |
rs151014772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50506552 | GGATTGAGTAGCTTC[A/T]CTTCTGTACTATATT | 11124 |
rs151016728 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FAF1 | GRCh38.p7 | 1:50889361 | TTTTGTGTCTCTATC[C/T]CCTTCAGTTCTGCTC | 11124 |
rs151022250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50853356 | GTTTTGACTCTTCAG[C/T]GTATATGACTGTACT | 11124 |
rs151024892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636459 | GGTGCGATCTCAGCT[C/G]ACTGCAATCTATGCC | 11124 |
rs151029328 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50605290 | GTACTTCATTACTTA[C/T]TGATTTTAGTGAGTA | 11124 |
rs151034059 | in-del | -/AGAA | 0.029116 | 0.117091 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465108 | TGAGATATAACAGAA[-/AGAA]TCACTACCGTCACAT | 11124 |
rs151037685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50868484 | CTTCCAGCTTCTTAC[A/G]GTGGAAGTATAGAGC | 11124 |
rs151042864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50766897 | TAAGAACTCTGCCAA[C/T]TTAAAAAGCCACAGT | 11124 |
rs151043638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652093 | GGAGGTGTGGGCAGG[C/T]ACCACTTCACAGGTT | 11124 |
rs151066911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464792 | TCCTCACTTGAAAGA[C/T]GAAGTAGCTGAAATA | 11124 |
rs151071184 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50491680 | CATTTAAATAATGAA[A/C]AATTGAGTTCTTTAT | 11124 |
rs151079216 | in-del | -/AAT | 0.146602 | 0.227616 | intron-variant | FAF1 | GRCh38.p7 | 1:50681025 | AAACACTACATTCAG[-/AAT]AATAATAATAATAAT | 11124 |
rs151084141 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50526087 | AGAAGGTAATTGATA[C/T]CGTTTGCGATATTTC | 11124 |
rs151095672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773461 | AACAGATACAAAAAT[A/G]TGGTATATACACAAT | 11124 |
rs151098462 | in-del | -/CTCTGG | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50763319 | AATGTATCTTTGTTT[-/CTCTGG]CTCTGGCTGCTTTCA | 11124 |
rs151099649 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50656631 | CTCACGCCTGTAATC[C/T]TAGCACTTTGGGAGG | 11124 |
rs151132239 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50798042 | ATTCTTTAAAGTCCA[C/T]GCCATGGCAAAATTT | 11124 |
rs151154434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50536746 | TCTAGTACCTGGAAA[C/T]TGGCACATGACAAAG | 11124 |
rs151161198 | snp | A/G/T | 0.0115307 | 0.0752106 | intron-variant | FAF1 | GRCh38.p7 | 1:50882705 | AATACTAGGTTAATG[A/G/T]CTGGGTGCGGTGGCT | 11124 |
rs151162631 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50955851 | ACATATATGACTCTT[A/G]GGCACATTATGCTAA | 11124 |
rs151167041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50661238 | AGCCTGTCACACTGG[C/T]TTCCCAGAAAACTAT | 11124 |
rs151168256 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50747937 | TTGCCTTCCACCACG[A/C]GTAAAGGCTCCCTGA | 11124 |
rs151182822 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50719308 | CTGCTACAGTTGTTA[A/T]CATCCTCCAAGACAC | 11124 |
rs151187699 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50599362 | GGTGATCTGCCCACC[C/T]CAGCCTCCCAAAGTG | 11124 |
rs151195938 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50859324 | GAAGAAGTCAAACTA[A/T]CTCACTTCATAAATA | 11124 |
rs151198187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50943615 | GCCTAGTCTAATTGA[A/G]TGACTCCCCTTATAA | 11124 |
rs151214223 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50887067 | CGTTTTTAATGATCG[C/T]CATTCTAACTGGTGT | 11124 |
rs151218958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50665263 | TGAATCAAGAAATAC[C/T]GTGGACCTGAAATGT | 11124 |
rs151223218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585855 | ATAATTAGCCTGGGC[A/T]TCATGGCCAGATCTC | 11124 |
rs151233183 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50807287 | AAGAATTACTTCAGA[A/C]TGGGTAATTTATAAA | 11124 |
rs151235690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50679276 | GCTGCTCTGCCTATG[C/G]AGTAACCATTCTTTA | 11124 |
rs151240165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50560572 | AACACTGCTTAGAAA[C/T]AGTGTGCAATGCCTG | 11124 |
rs151244485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469086 | ATTCTTTTAAACCTT[C/T]TGCTATTTACTTTTT | 11124 |
rs151246280 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938874 | GTCAAATATCAGTTG[C/T]AGAAGTGCAACTTTT | 11124 |
rs151251112 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50908903 | TTGTTATGTGTGAAT[C/T]TGATCCTGTCTTCAT | 11124 |
rs151256353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610026 | GTGATTTGAATTAGT[C/T]TGCTAAATAAATTAA | 11124 |
rs151257493 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50691305 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 11124 |
rs151306017 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733970 | CCCAGATAATTTTTG[C/T]ATTTTTAGTAGAGAT | 11124 |
rs151309226 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50614637 | CTAAGGTCAGGAGTT[C/T]GAGACCAGTCTGACC | 11124 |
rs151309470 | in-del | -/TCTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527812 | GAACTTACTCTGCTG[-/TCTC]TCTCTCTCTCTCTCT | 11124 |
rs151310568 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50530678 | ATAAATGCTTGAGGA[C/G]ATGGATACCCCATTC | 11124 |
rs151319106 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50952307 | TGGAGACGGGTTTTC[A/G]CCGTGTTGGCCGGGC | 11124 |
rs180679114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50730107 | GGTTGGAGCAGCATG[C/T]GGAATTTTTGACAAC | 11124 |
rs180682889 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50777270 | TGAAAAAAAAAAAAA[A/T]TTGCCAAACATGGTG | 11124 |
rs180692133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751186 | CTTAGAGCAAAGTAG[C/G]AATATAAGGCAGCTT | 11124 |
rs180695197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50790135 | CACAAGAATAAAGCT[C/T]TTATTTGTATGTTTT | 11124 |
rs180700872 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50767941 | GGATCAAATCCACAC[C/T]TATCAATATAAACTT | 11124 |
rs180703459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810960 | TGAGGCAGGAGAATC[A/G]CTTAAGCCTGGATGG | 11124 |
rs180711063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50827872 | CAAGTTCAATAAATG[A/G]AAGGATATTCTATGT | 11124 |
rs180788775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50449054 | TAACATAAAGCCACA[A/G]CAAAGATTATTCTTA | 11124 |
rs180789493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463556 | ATGTGTGTGGTGCTG[A/G]AAATAGCACTTAATA | 11124 |
rs180795646 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441150 | AATTCTATTTAGTGA[C/T]CACTCACACTTGAAC | 11124 |
rs180803026 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50953361 | CCTGCCAAATCCCCC[C/T]CTCCGAGAAACACCC | 11124 |
rs180816823 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50939062 | GGGCTCATTTTTGCT[G/T]CCATGTGAATTTTAG | 11124 |
rs180817210 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50895024 | AGAAGAAGAGAAATA[A/T]TAAAGATCAGAGCAG | 11124 |
rs180818538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50880833 | ATGAGTTGTTCAGTC[A/G]TAGAGTTACCATCAT | 11124 |
rs180821719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50928592 | TTCGAGACCAGCCTG[G/T]CCAACATAGTGAAAC | 11124 |
rs180823416 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50921154 | AGGTACACACTGTCC[A/G]GGGGCCTTAGGTTGG | 11124 |
rs180823513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50903922 | TCACAAAACAAGCTA[C/T]GTACATGAAAACTGT | 11124 |
rs180825109 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50862810 | AGGGACATTATATAA[C/T]GATAAAGGGACTAGT | 11124 |
rs180828216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886532 | ATCCCTCCCCACTCC[C/T]CCCACCCCACAACAG | 11124 |
rs180833216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842960 | TGCCACATCCCCTGT[A/G]CCTAAAACAGTGCTA | 11124 |
rs180834373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528323 | CTGCTTTTAGCAATA[A/G]ATTTTTTACTTTAGT | 11124 |
rs180842920 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50948430 | AGGCAAAGCGGGAGA[C/G/T]AGCCTCTCACAGTCA | 11124 |
rs180845588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505352 | CAATAGAGAGAGACA[A/G]CCAAACACCTATTCC | 11124 |
rs180851633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50912054 | AAAAAAAAAAAGGCA[A/G]AGTATTTAGAGGACC | 11124 |
rs180855254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50484850 | ATCTTTTTAAAACTA[C/T]TGTTTTTTTTAACCA | 11124 |
rs180857498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50870195 | GGCACATTGGCTCAC[A/G]CCTATAATCCTAGCA | 11124 |
rs180866247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657499 | CCCAGCAGATAGAGG[C/T]AGCAATGAGCCACGA | 11124 |
rs180867352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598181 | CACGCCTGTAGTCCT[C/T]GCTACTTGGGTTGCT | 11124 |
rs180875482 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576739 | GCTAGACCTTCTGGG[C/T]TCAAGTGATGCTCCT | 11124 |
rs180876687 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50553406 | ATAAGGACTTAAGAC[A/T]CATTTGTGGGTGATA | 11124 |
rs180878909 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50669788 | ACCACATATGGCTAC[A/T]GAGCACTTGAAATGT | 11124 |
rs180879577 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50588017 | GTCAGCCAGGCATGG[C/T]GGCTCATGCCTGTAA | 11124 |
rs180882307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50638589 | GCTGAGATTACAGAC[A/G]CCCACCACCATGCCC | 11124 |
rs180891213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687861 | CTAAAAAATGAAACA[C/T]GCGGTGGCTCACGCC | 11124 |
rs180893338 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50618716 | CTTAATTTTTACTAA[C/T]ATTTGTTTTATCGAA | 11124 |
rs180898815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50629029 | TGCTGGGAAGGTTAA[A/G]TGAGTTATTATATGT | 11124 |
rs180903343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695433 | CCACTGTATTAACAT[C/G]TAAAGGAGGCTTATT | 11124 |
rs180904759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50735193 | GAATCTTTCCTGTAA[C/T]AATATGAAACAGTAT | 11124 |
rs180908240 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50607589 | CTGGGTTTCCCTCAC[C/G]ATTCTTTTCCATCTG | 11124 |
rs180909842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848702 | TGTGATATTCTTTCC[A/T]AGAATGCATAAACTC | 11124 |
rs180910843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50726434 | GGGCACGGTAGCTCA[C/T]GCCTGTAATCCCAGC | 11124 |
rs180914182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50705717 | CCAGAACAGATAAGC[C/T]CTCTTTAACAGGGTC | 11124 |
rs180925142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50795392 | TGATGGCTTCCCACA[A/C]AACCTTGGTTCTAAC | 11124 |
rs180925351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50746768 | GCTAAAACAATGAAG[A/G]AAAGGCCTCACAGGC | 11124 |
rs180928356 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50763321 | TGTATCTTTGTTTCT[C/T]TGGCTCTGGCTGCTT | 11124 |
rs180929932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50815010 | TTATCATATGGTGCA[A/G]CAATTCCACTTCTGG | 11124 |
rs180931403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50782179 | AAGTATACACTTTCT[C/T]TTTGTTTTTTTTAAG | 11124 |
rs180934698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50830880 | GAATCTTTTTTGTAA[C/T]CTAAACCCATTTGGA | 11124 |
rs180935069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50678608 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11124 |
rs180943890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50715803 | ATACATTTTACATAC[C/G]CCTCCACATTTTTTA | 11124 |
rs180956314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648288 | CAAAACAAAACAAAA[A/T]AACAAAAAGGTCTTC | 11124 |
rs180973140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50754223 | GGATATTTTTGTAAT[C/T]CTATAAATATTCCTG | 11124 |
rs180981540 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50807064 | GCTGAAACGAAAGAA[A/G]CAGAATTGAAAGTAT | 11124 |
rs181012821 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50824023 | TGTGTTCTGGAAAAT[G/T]ATAAAGGAGACTAAA | 11124 |
rs181028116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515811 | CTGTCTATAAACAAC[A/C]CCTTCTTGCCTTATT | 11124 |
rs181033363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50444196 | TGTTTCTCCCCAGCA[A/G]GATGGTGGCCATGCT | 11124 |
rs181036679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495155 | TATTTTTAAATGTAC[A/G]ATGATTTTTACTATA | 11124 |
rs181052339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471524 | AGAGATAAAAACCTA[C/G]AAAGCTGGGGCAAAA | 11124 |
rs181055886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50565406 | CAGTCCTGCAGTTCA[C/T]TGAGAAATAGCTCTA | 11124 |
rs181056967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541779 | AGAGAGAAGAGAAAT[A/T]AAAAAAAAGGGAAAA | 11124 |
rs181060429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468182 | TCACTGCACTCCAGC[C/T]TGTATGACAGAGTGA | 11124 |
rs181079262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939908 | ATAAAAGTACTTTTT[A/T]ATTTTCTTGTTTTTT | 11124 |
rs181079826 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50586484 | AGCATTAATGCAGAG[A/T]ATCATAATCATATTT | 11124 |
rs181095751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948064 | ACTCAAAAGAAGAGA[C/G]ATGTACAAAATAGAA | 11124 |
rs181112493 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928342 | AGTATATGGAGAAAA[G/T]AACGTCAAGAATCTA | 11124 |
rs181120677 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50506043 | TACATGTGCCAATAG[C/T]AGAAAGTCTTGAAAA | 11124 |
rs181121060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50529372 | TGAATGCTTGCCAAG[A/G]CAAAACAATCAATGC | 11124 |
rs181128823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50441630 | AACTATGCACTGGCA[C/T]GAAGAGTCTCGCAGT | 11124 |
rs181130809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894522 | AGCTGTTACTTAAGG[C/T]GCAAGAAAAACTTAT | 11124 |
rs181131498 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50911898 | AAAAATCAATCAGGC[A/C]TGGTGGCATGCCCCT | 11124 |
rs181133134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50485922 | AGATCTTGTGAGAAC[C/T]CCATCATGAGAACAG | 11124 |
rs181133762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464405 | GTGACTTGCCCAAGG[C/G]CCCCCTAATAGTTGG | 11124 |
rs181139683 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50628504 | TTAACTGGGGATATT[G/T]AATATCATTTCTTAA | 11124 |
rs181140451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50577422 | CCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA | 11124 |
rs181149140 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50553968 | AAGCACAGGCTGGAG[A/C]AACATCAGCTAAGCA | 11124 |
rs181150887 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50879857 | GTTTAAGAACCACTG[C/T]CTTAATTGGCTAAGG | 11124 |
rs181155720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50861009 | CACCACATTTTCTCA[C/T]TTATAAGTGAGAGCT | 11124 |
rs181156271 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50639396 | TATACTACTTTGCCT[C/T]CCTACCTTGCTGATA | 11124 |
rs181159780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606153 | AGGATTATCATATAG[C/G]TGTTTTCAGTTGCAA | 11124 |
rs181164535 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50842434 | CATTCTTAAGCATAT[A/C]TTTTAATACTACATG | 11124 |
rs181165849 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50667674 | ACAGACAAATTAAGC[A/T]ACTTGCCTAAATGTC | 11124 |
rs181172742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50618852 | CTCCTGGGTTCCAGC[A/G]ATTCTTCTGCCTCAG | 11124 |
rs181175566 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50679004 | AAGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 11124 |
rs181179793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50647432 | TTGTTCTAACCACGA[A/G]GCATTCCTGGAGTCT | 11124 |
rs181181498 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50598954 | CAACCTGGACAACAA[A/G]AGTGAAACTCCGTCT | 11124 |
rs181183784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687441 | TCTATAAATGGTCAA[C/T]AAACACATGAAATGA | 11124 |
rs181186388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50658530 | ACATTCCTTTGCTAT[C/T]CTAAGCCTGAAAAGC | 11124 |
rs181188670 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50695896 | TCAGGTGATCCATTC[A/G]CCTCGTCCTCCCAAA | 11124 |
rs181194226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725252 | TTTTTTGGTAGGATC[G/T]GAGGCCCCGTGCAGA | 11124 |
rs181197983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824608 | GATGTAGCAATTCCA[A/C]TGCAGGGTATACATC | 11124 |
rs181199380 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50736487 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11124 |
rs181199474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50716470 | CTGGACTTCCTGGGT[C/G]GAGTGGGGACTTGGA | 11124 |
rs181207025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705185 | GGCTGGGGCCCAAGG[C/T]ATACCAACAAGGTAC | 11124 |
rs181232743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50755105 | GCCTTCCCAACAGTC[C/T]CCCAAAGTCTTAACT | 11124 |
rs181247617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50795609 | AGTGTCCAAAACACC[A/G]CACTATTTTTCATAC | 11124 |
rs181257923 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50832263 | GGTGCTAAAAAGGTT[C/G]GGGACTGCTGATTTA | 11124 |
rs181259205 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50772541 | AGAATGAGATCATGT[C/T]CTCTGCAGCAATATG | 11124 |
rs181271007 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50446104 | ATGTTTGGGGTTGTG[A/C/G]GGGGGAAGCTCCTTA | 11124 |
rs181291784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50899313 | ATAACTTTTAATGAC[A/C]TTCTATCATCTATAT | 11124 |
rs181301935 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50883211 | TGAACATCAAAAATA[A/G]AAATGTCTGAAATAA | 11124 |
rs181305349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815322 | TGCTTACGTGAGAAT[A/G]TGCTTTGGTCCTGAG | 11124 |
rs181306695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50867567 | ATACAAATGGCAAAA[A/G]AAAATGAAAAAATGC | 11124 |
rs181311789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846148 | GAAACGAAAAAGGAA[A/G]GAAAGGGAGACTCGT | 11124 |
rs181323325 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468441 | GGGATTACAGGTGCA[C/T]GCCACTACACTTGGC | 11124 |
rs181339555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925184 | AGGAATGAAACTAGA[C/G]CCCTATCTATCACTA | 11124 |
rs181345923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50944782 | TGCCACATAGAAGAT[A/G]GATACCAACCAGGCT | 11124 |
rs181349219 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50510990 | GACATATTTTATCTA[C/T]TAAAAAGTCCCCAAA | 11124 |
rs181361503 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50950150 | TGTCCCAGATCACCA[G/T]TTTATAGACTGAATA | 11124 |
rs181363124 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50915919 | TAAAAATCCTTTTTT[C/T]TTCCCCTAAAGCTGA | 11124 |
rs181365037 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50890596 | TGCTTGTCTATAAAG[G/T]ATTTTATTTCCCCTT | 11124 |
rs181365956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523199 | TTTCCACTTTTTGGC[G/T]ATTATGAATAATGAT | 11124 |
rs181377294 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50592038 | TATGCTAGGTGTTAG[C/G]GCTACAGAGGGGAGA | 11124 |
rs181382832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50643467 | GTTTCTATTGCTGTA[A/T]CTTTAAATTCACTGA | 11124 |
rs181385877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50572262 | TCTTTTAATACTTCC[C/T]TGAAACATCTGAATG | 11124 |
rs181388967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50561558 | TGTGGCCGGGCGCAG[C/G]GGCTCATGCCTGTAA | 11124 |
rs181389796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50549947 | ATCATTATATAAAAT[A/G]TTTCAGCATCATTTA | 11124 |
rs181390854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50623435 | TTAGCTGGGTGTGGC[A/G]GCGTGCACCTGTAGT | 11124 |
rs181411693 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50662486 | ACTAATTTAAATATA[C/T]TAAGTTGGAGACGGA | 11124 |
rs181413659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50614615 | GAGGCCAAGGTGGGC[A/G]GATTACCTAAGGTCA | 11124 |
rs181413870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50699440 | ATATTCCAAAGTAAG[A/G]TTATTAATTATACAA | 11124 |
rs181416627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50683073 | ATATAGTGCACTTAT[C/T]TTATCCAAAATTTAA | 11124 |
rs181419110 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50601661 | CACTCCAGCCTGGGT[A/G]AGACTCAGTCTCAAA | 11124 |
rs181425461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50719895 | GTACCTCACTCCAAT[C/T]AGATGTGTTGTGATT | 11124 |
rs181431954 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739394 | TACATATATGTGTGT[G/T]TATGTGTATGTGTAT | 11124 |
rs181434603 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757530 | TTCATAATATTCTTT[G/T]TCCAGAGTCTAGCTC | 11124 |
rs181437878 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717300 | CAGGTTTAGGTGAGG[C/T]CATGAGAGTGGGGCC | 11124 |
rs181442792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50635130 | CTATTTCCTGACACA[C/T]TAATAATATGGCTAC | 11124 |
rs181454422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50736659 | AGGAGGCTGAGACAG[A/G]AGAATTGCTTGAACC | 11124 |
rs181454997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674398 | CTTACTTGGCTAACT[C/T]TTCCTTCATATATTT | 11124 |
rs181456442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50710160 | ACCTTTACATATGAA[C/T]CTATGCATATGTTTA | 11124 |
rs181462472 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50755528 | CACGGTGCAAGCTGT[C/T]CGTGGATCTACCATT | 11124 |
rs181468365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773404 | CAGGATTATTCACGA[C/T]AGCCAAGAGATGGGA | 11124 |
rs181470524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50446715 | ATATTTCTGAGGTAA[C/T]GCTTTTATTTTGAAA | 11124 |
rs181472739 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50797005 | GCCGGGCTTGGTGGC[A/T]CATGCCTGTAGTCCC | 11124 |
rs181473840 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50746179 | GGAACAAAGCATTCA[A/G]GATGTTGCCTGGCTG | 11124 |
rs181479159 | snp | G/T | 0.119978 | 0.213528 | intron-variant | FAF1 | GRCh38.p7 | 1:50907919 | CTTCTGCTAGCTTTT[G/T]AATGTGTTTGCTCTT | 11124 |
rs181482388 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | FAF1 | GRCh38.p7 | 1:50780878 | GAGGAGTCACAGAAG[A/T]GGTGGAAGCCAAACA | 11124 |
rs181484245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50932447 | AAATCCAGCGGGGCA[A/G]TTAAATTTTAAAGCG | 11124 |
rs181484271 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50489206 | TGTAATATCTTCTTA[C/T]AGGCAGAAAACGTTT | 11124 |
rs181485171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815659 | AACTAATTTACATTT[C/T]TACCAACAGGGTATA | 11124 |
rs181491002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833932 | ATTACTCTCTTAACT[G/T]GTCTCTCTGCATTCA | 11124 |
rs181499017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50511573 | CCCTGAAAAGGACAC[A/G]AACTCATCCTTTTTT | 11124 |
rs181500023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822981 | GTTTCTCCACGTTGG[C/T]GAGGCTGGTCTCCAA | 11124 |
rs181506627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570691 | CATAAGCTTTCAACA[A/G]AAAATTTTCTGCTGC | 11124 |
rs181510241 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50581879 | AGAGCTGAAGCTACA[A/T]AGATAGGCAGGAGCC | 11124 |
rs181513601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50490394 | CTCAAAAAGGAAGGA[A/G]GGAAGGAAGGAAGGA | 11124 |
rs181521090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50536198 | AAGAAGGTATTTTTA[A/C]TGTTTGATTTTCTTT | 11124 |
rs181540618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612029 | TGGTGAACGAAAACA[G/T]TTCGATGGTAATCTT | 11124 |
rs181545402 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561856 | GGATGGACGGAAGGA[A/C]GGAAGGAAGGAAGGA | 11124 |
rs181549150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50537277 | TAGGCTTAAGTCACT[G/T]CTTATCAGCTATGTT | 11124 |
rs181552429 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50591230 | TATTACATTGAGGAT[G/T]CCATTATCTCTTGCT | 11124 |
rs181561326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944496 | CCATTCCAGCAGCTA[C/T]AACTTCACCTTTTTC | 11124 |
rs181564343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50653439 | CACTGCAACCTCCCC[C/T]TCCCAGGTTCAAGTG | 11124 |
rs181567984 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50652105 | AGGCACCACTTCACA[A/G]GTTCTGGGACAAGGT | 11124 |
rs181578068 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907383 | TTGGTATCAGGATGA[C/T]GCTGGCCTCATAAAA | 11124 |
rs181578747 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50924972 | TGGGTGACAAGAATG[A/G]AACTCCATCTCAAAA | 11124 |
rs181585468 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50691748 | GGCATGCACCACCAC[A/G]CCCGGCTAATTTTGT | 11124 |
rs181589508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50889891 | TAGGTCCGCTTGATG[C/T]AGAGCTGAGTTCTAT | 11124 |
rs181590970 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50875064 | ACCATGTTTTTTATA[C/T]TTTTACATTATATAT | 11124 |
rs181598947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50853909 | ACTGCTATTCATTGA[A/T]TTTTAACAAAAAATT | 11124 |
rs181605109 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50837657 | ATTGACCTATAAAGT[G/T]TGTACCAAATACATA | 11124 |
rs181609616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50763215 | GTAAGCCGAGATGAC[A/G]CCACTGCACTCCAAC | 11124 |
rs181623681 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50806710 | CCAGACAAGAATGCC[A/G]GGGGCCTGGTGTCAG | 11124 |
rs181640473 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50455051 | GACCTCTTCCCCCAG[C/G]CTCATTCCTACAGCA | 11124 |
rs181642433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50720961 | CCATATAAGTTTCAA[C/T]CATTTGATCATTCTT | 11124 |
rs181659804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50498369 | TGATTTCTTTAGTAC[A/G]TCATTGAAAGCATAA | 11124 |
rs181659964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50740979 | ATTAAATTTTCCCAT[C/T]AAACCACATATGGAA | 11124 |
rs181662988 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50757916 | GTGATTGCTCTAAAG[A/T]TTACAACATAATTTT | 11124 |
rs181666344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777904 | AATGTTTTGCTACAC[C/G]TGCTAACTCTAAACA | 11124 |
rs181668071 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447360 | TCGATCTCCTGACCT[A/C]GTGATCCGCCCGCCT | 11124 |
rs181676557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50800620 | TATCATTGCTTTCAT[C/T]TAAAAACCATCAACC | 11124 |
rs181680644 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960520 | GGGGACCAGATTGTG[A/C]ACCTCACGTGGTTAG | 11124 |
rs181682573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50819245 | TGATAGAAATCTTGA[C/T]TGAGGGAGGGGGGAT | 11124 |
rs181686071 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50450101 | CAGGAGGCTGAGACA[A/G]GAGAATTGCTTGAAC | 11124 |
rs181694271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50546873 | AACTGCATGTAATCC[C/T]AAACCTTTAACAGTG | 11124 |
rs181710172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50582472 | AGCATGGCCCATGCA[C/T]AATGATGACATACAA | 11124 |
rs181719119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897855 | TGAGAAGTACCATGA[C/G]TTTCTGCTTGCAGTC | 11124 |
rs181724592 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50950386 | CTGATTTCATGGGGG[G/T]AGCGGAGAAATAACT | 11124 |
rs181726610 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50623974 | AAGAAGAAGAAAGAA[G/T]AAGAGGAAGAAGAGG | 11124 |
rs181732245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932982 | GTTGGCCCATTTCAG[A/C]CATGGCTGGAGCGGC | 11124 |
rs181732616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866403 | GGAAGTCAAACTGTT[C/G]ATGTTTGCCGATGAT | 11124 |
rs181744654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50900151 | AGCTAGGAAACTGTA[C/T]ACATTCTCTCTCTCA | 11124 |
rs181747431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916425 | TAGGACTTATCTTCA[C/T]ATACAAACACCTCGA | 11124 |
rs181760532 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50884280 | AGCACTTTGGGAGGC[C/G]GAGGCGGATGGATCA | 11124 |
rs181762776 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50663056 | AAAGACAATTCCTAA[A/C]GTGCTAAGAAAATGT | 11124 |
rs181763744 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50535603 | GTTAAAATACTTTTG[C/T]GGTTTTATTGAAATG | 11124 |
rs181767110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50476665 | TCATCTAAAGCAGTG[C/G]TCTGATGAAATTCAC | 11124 |
rs181771185 | snp | A/C | 2.06392e-05 | 0.00321235 | intron-variant | FAF1 | GRCh38.p7 | 1:50475705 | CAAAAACCAGGTGTT[A/C]AAATGTGAGAAGGAC | 11124 |
rs181772310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50510282 | TGTAATTGATGACTA[C/T]TAACCTAATAATAAT | 11124 |
rs181786683 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50700087 | CCTCCCCAAAAATAA[C/T]GCACTTGAAAAACTC | 11124 |
rs181794095 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50673454 | ATAGCAGGAAGGTAT[A/T]ATTTTGTAGTAGTGA | 11124 |
rs181797259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456365 | TCTGGTGCTTGAGTT[C/T]TAGAAACTCCATGCT | 11124 |
rs181802533 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50663828 | ACTTTTGAGAATAAA[C/T]ATAATTAATAATCAT | 11124 |
rs181804292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691098 | ATCTAGGAGTAGAAT[C/T]GCTGGGTCAGATAGA | 11124 |
rs181804967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50499580 | CATCTACAATGAAAA[G/T]GAAGTAGAACTCTCT | 11124 |
rs181811624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50522046 | ATGTAAACAGGGACG[G/T]TATGGATATATCTTT | 11124 |
rs181815853 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | FAF1 | GRCh38.p7 | 1:50729320 | TCGGCCTCCCAAAGC[A/G]CTGGGATTACAGGTG | 11124 |
rs181816031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644699 | TTCCTTCTTCAGAGT[C/T]CTGTTGGCTAATATC | 11124 |
rs181822147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50710004 | GAAAGCAATGAGGAA[A/G]AAGTGTAAGGTGATG | 11124 |
rs181829065 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50852630 | AAAATGTGGTTTACC[A/G]CTATGACAATTCCTC | 11124 |
rs181830193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768314 | GTTCTTAGAGATCTA[C/T]AAAGAGACTTAAGAT | 11124 |
rs181834300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50837468 | CATGATTAGATTCAG[C/T]TAAATATTTTTGGCA | 11124 |
rs181841543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50789864 | CTATGCTAACAGGCG[C/T]ATGGTCTTTCATTTC | 11124 |
rs181848698 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50811086 | ATGGCTGTAATTCCA[A/G]CACTTTGGGAGGCTG | 11124 |
rs181918294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50882933 | GGGTTGTAGTAAGCC[A/G]AGATTGCGCCACTGC | 11124 |
rs181932484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644051 | CTTCCATGTCTGTTT[A/C]TTTTGACTGACTTCT | 11124 |
rs181934341 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50488779 | TTATAAAGATAAATC[G/T]CTAACCTTGTAGCTT | 11124 |
rs181939823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602214 | AAATACAATTCTCTT[A/G]TGTTTTAAGAAGAAC | 11124 |
rs181940821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50944127 | GAGATGGGAGTAAAG[A/G]AGTGTTCACAGGTGT | 11124 |
rs181948588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50522238 | ATTCAGTTTATCCCA[C/T]AAATCTTTAATATAA | 11124 |
rs181960543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906873 | GAATCCCCTTTCTTT[A/C]TTTCTCCTGCCTGGT | 11124 |
rs181961322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50483178 | GCAATATATGAATTG[A/C]AGCATTTTAAAACTG | 11124 |
rs181961772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50566215 | AACAAAGTCTGAATG[A/T]TGACCAAAAATTCAG | 11124 |
rs181963019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845921 | TGAGGTCAGGAGTTC[A/G]AGAACAACCTGGCCA | 11124 |
rs181963473 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50613183 | CCTGGAAACCACTCC[A/C]AAGTGAGATAAACAC | 11124 |
rs181967494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846604 | CCTGGGTGAGTGAGC[A/G]CTTCCTTGTAAGATC | 11124 |
rs181968302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50543251 | CTTTCACCAAGCTAT[A/T]CTCTAACATAAAATA | 11124 |
rs181973538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874544 | TTCTTTACTTTTCGT[A/T]GAAATGGAGTCTCAC | 11124 |
rs181976729 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50571435 | CATCGCAGATAATGT[A/G]GGTTAAGTACCTATT | 11124 |
rs181979872 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50652998 | TTAATTATCTTCTTC[C/T]ATTAATATTACTATT | 11124 |
rs181986485 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50606643 | TAGCTGGGATTATAG[A/G]GATGCGCCACCACAC | 11124 |
rs181988635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462822 | GGACTAAGTTATGTT[C/T]GAAGGTGGGAAGTTT | 11124 |
rs181989560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50628745 | TTTCATCTCACATTC[C/T]ATAAAAATGGAACTA | 11124 |
rs181991232 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50587775 | ACCATATATTATACA[C/T]AGAGTGATTAGTGCT | 11124 |
rs181993869 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50504326 | AAGAGATCATGTTTT[G/T]GAATTTTCTAGTATA | 11124 |
rs182001492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927678 | GAATGGAAGAAGGAG[A/G]CTTCTGGAACTCTGA | 11124 |
rs182002772 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50947808 | TATTTTCTCAATGAC[A/C]GATTTTATTATTCAA | 11124 |
rs182006711 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819668 | CACACACACACACAC[A/T]CTCTCTCTCTGTATA | 11124 |
rs182010424 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50684669 | TCAGATTCACAAAAT[A/C/T]CCTGAATATTTAATA | 11124 |
rs182011019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687601 | CTAAAAATACAAAAA[C/T]TAGCCAGGCATGGGG | 11124 |
rs182015295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50647646 | ACCATGTTAAGGCAT[C/T]CTTTCTAGTACATAC | 11124 |
rs182016727 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50684105 | TTTCCAACTTGGAAA[C/T]TGAAAGGTGAGTTAG | 11124 |
rs182017912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669109 | ATTAAGACTCAGTGA[A/C]CCTACACTAAATTTA | 11124 |
rs182018640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50911154 | CTCAGCTCACTGCAA[A/C]CTCTGCCTCCCCAGT | 11124 |
rs182020175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893430 | TGTAGCTCTTACAGA[C/G]TTCTAGAGGTATTGC | 11124 |
rs182033773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50879256 | TTTCAAAAAATAAAC[A/G]AATGAATGAATGAAT | 11124 |
rs182036796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50859953 | AAGCTGCTTGCACAA[C/T]TACAGCCATTTGATC | 11124 |
rs182041087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50702271 | TTTGTAACCACAGAT[A/C]TTTAATAGTATTAGT | 11124 |
rs182041723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721581 | TTTCAAAAAACTTAT[C/T]TACAGGCCACTTTAA | 11124 |
rs182046857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841459 | CCTTTGTGTTTCCAT[A/G]TAGTTTTAAATTTTT | 11124 |
rs182052385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685412 | GGAGGGTGAGGTAAA[C/T]TACTGCTATAGTATA | 11124 |
rs182055476 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50637520 | TCTTTCACATTTCCA[C/T]ACAATTTTTGGAATT | 11124 |
rs182055655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722119 | CACAGGAGTCCCCCA[C/T]TGGCAATTGCTCATC | 11124 |
rs182059720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758867 | TATTATTTTGAGATG[A/G]AGTCTTGCTCTGTTG | 11124 |
rs182067132 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50760012 | TTGTTTGTTTTTTTC[C/T]TGTAAATTTGTTTGA | 11124 |
rs182070026 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50742741 | AATAACTACAAAAGC[A/G]AACTCATTTTGGTGT | 11124 |
rs182070765 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | FAF1 | GRCh38.p7 | 1:50827500 | ACACTGCGGAAGGCC[C/G]CAGGGACCTCTGCCT | 11124 |
rs182072724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50801978 | CCAAAGTTTAAGGAT[A/G]TCAAAACAGGAAAAA | 11124 |
rs182080435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778705 | GGTTGGTCTTGCTAT[A/C]TCAGGGCTGGCAGAG | 11124 |
rs182083449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50790720 | ACCAGCTCTAAAACA[C/T]CTTTCCTCTCAACCT | 11124 |
rs182164174 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50829123 | GCTGACAGGTAGTGA[C/G]TGGCAAGAATGTAGA | 11124 |
rs182184325 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472812 | GATGACTTTTACAAA[G/T]TAGATCCTAATCCTT | 11124 |
rs182185111 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50507575 | CGAGACCCATAAAAA[A/G]TAATTTAAAAATTAG | 11124 |
rs182192655 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50914626 | ATGTATCAATCACTG[C/T]GCATTTAATTATATT | 11124 |
rs182192807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50955492 | TTTGCTCAGAGCTGA[C/T]TTTTAAAATAATTTA | 11124 |
rs182203612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50552874 | ATCCCAGTAGGCTTG[A/C]CCAGCATTATTGTGT | 11124 |
rs182204954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50953842 | CAAAAGCACATTTGT[A/G]TGTTACAGAAAACAT | 11124 |
rs182206565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50922947 | GAAGTCATCATAACT[C/G]ATACCAAAGAAACAC | 11124 |
rs182212163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922257 | TGAGGTCAAGGAGTT[C/T]GAGACCAGCATGACC | 11124 |
rs182213152 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50558399 | GTGGGGTCGGGGGAC[A/G]GGTTACAGAATGGGG | 11124 |
rs182213253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50532949 | TCTGAGTAGCTAGGA[C/T]TACAGGCATGCACCA | 11124 |
rs182218500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549292 | CTAGCTGCCAAATTT[A/G]GAGACTTTGTTTTTT | 11124 |
rs182222358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50597229 | AGCGAAAAGGATGGA[C/G]TCTAGAAAACATGAC | 11124 |
rs182224958 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50958934 | AAGGCAAAGGTAGCA[C/T]TCACAGGATATTAGT | 11124 |
rs182225872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621682 | TGAGATTACAGGAGT[G/T]AGGCACTGCACCTGG | 11124 |
rs182227749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50924090 | GACAAGAGGAAGAAG[C/T]AAAAGGTATCCAAAT | 11124 |
rs182231322 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50886784 | AGTCTATCATTGATG[G/T]ACATTTAGGTTGGTT | 11124 |
rs182233192 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940663 | TACTTTGCATTGATA[C/T]AGATTTATACTAACA | 11124 |
rs182236565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50579085 | CTGCTAAAACACCTA[C/G]ACACTAAGAAAAGCA | 11124 |
rs182237534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516345 | GGACTATATCCCTCC[A/G]TTTTGAACCAATCTG | 11124 |
rs182238143 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50599722 | TGAAGAAAAAGCATG[A/T]GTGTTTCAGTTATAT | 11124 |
rs182240758 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50867752 | GTAAACTAGTACACC[A/G]CTATGAAAAACAGCA | 11124 |
rs182242607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591493 | CCTGGCCAACATGGC[A/G]AAACCTCGTCTCTAC | 11124 |
rs182246062 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50889672 | CCATGTAGTTGAGCA[A/G]TTTTGAGTGAGTTTC | 11124 |
rs182249645 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50848984 | TTGTACTAAGCCAGG[C/T]GCAGTGGCTCATGCC | 11124 |
rs182255449 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640779 | GGCACTGTTAATTCA[C/T]ATCTAGTCTCTTTTT | 11124 |
rs182263036 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50660058 | TAAACACAGCACTGG[G/T]GGAAAGATCATTTCA | 11124 |
rs182278267 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50634561 | CAGTTATAAAATAGG[G/T]TTGGGTACAAGGCTG | 11124 |
rs182288310 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50473139 | ACCACAGGGAGATAG[C/T]AGCAGGCCCAAGAAC | 11124 |
rs182321250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50705585 | GTTTAAAAATTATCA[A/G]GAGTTCCCATTTACA | 11124 |
rs182326655 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742397 | GGAGGGGGGGTGTGG[C/T]GGGGGAGAGAGACTC | 11124 |
rs182365130 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601753 | ACATATATTCATATA[C/T]ACACATATATATTCA | 11124 |
rs182366862 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677072 | TAGTCACTTTATAAT[C/T]GAATAAATACTAAAG | 11124 |
rs182376019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50689817 | AACATGCCATTCTAT[C/T]TTCTGTTACTTTATT | 11124 |
rs182383274 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819741 | TATACATATATATAC[A/G]TATATATATACATAT | 11124 |
rs182384988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728160 | AGGGATAAAGCAAGA[G/T]AGAGAGAGGGTATAA | 11124 |
rs182390302 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50707995 | TTGTATTTTTAGTAG[A/C]GATGAGGTTTCACTA | 11124 |
rs182398757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749306 | ACACTCTTGAAAACA[C/G]TCTGAGCCCTCATGA | 11124 |
rs182411340 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50752691 | ATTTTTTTGGTTTTG[C/T]TTTGTTTTTTTGAGA | 11124 |
rs182411862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50765815 | GTAAAATAGGGCTAG[A/G]CATGGTGACTCACAC | 11124 |
rs182413838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816130 | GTGATTTTTTTTTCA[G/T]GTTGTTGGCCATTAT | 11124 |
rs182421491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50834327 | AGTTCTTTATAGCAA[C/T]GCAAGAATGGACTAA | 11124 |
rs182422901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786175 | TTCATTGCAGCGTTA[A/T]TCACAACAGCCAAAA | 11124 |
rs182425354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808742 | TATCTGATCTCATTA[C/G]TTTCAAAGAATTTCT | 11124 |
rs182435181 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50820201 | GCAAGATGAAAAAGT[A/T]CTGGAGATTTTTTTC | 11124 |
rs182443019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50450817 | TTACAATTATTAATA[A/C]TAATTATTATAAACA | 11124 |
rs182444880 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50793306 | CTTGCAGCTGTTTAC[C/T]AGAGTATCTGTGTGC | 11124 |
rs182459789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50952344 | CCAGCTCCTGACCGC[A/G]AGTGATCTGCCAGCC | 11124 |
rs182464355 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50495510 | TTATCCATTTGCCTA[C/T]TGATGGACATTTAGG | 11124 |
rs182471972 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50527793 | GATGAAGTATTTAAC[C/G]CAAGAACTTACTCTG | 11124 |
rs182475253 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50681861 | TCTTTTTGAGACAGG[G/T]TCTTGCTCTGTTCCC | 11124 |
rs182476131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937296 | TTTTGAAGTGTTTCA[A/T]TGACAGACAAGCACA | 11124 |
rs182481828 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50641790 | TCTACCTGTGTGTCA[C/G]CTTTGGCTTTGCGTA | 11124 |
rs182482879 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50939160 | TTGCTCTGGAGAGTA[C/T]GGCCATTTTAATGCT | 11124 |
rs182486104 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50904779 | AAAGATGAACTGCCA[C/G]TTTCCACAAACCTCC | 11124 |
rs182487493 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50697942 | ACTGTATAACACTGA[C/G]TCATACACAAGACAC | 11124 |
rs182489866 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50918909 | GTGAGATGATATCTC[A/C]TAGTGGTTTTGATTT | 11124 |
rs182491802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50901648 | AGGCAGGTGGATCAC[C/T]TTGAGCTCAGGAGTT | 11124 |
rs182494316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930644 | ATCGAGACCATCCTG[C/G]CTAACACAGTGAAAC | 11124 |
rs182499441 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576322 | GTGGGAAATCAGCAA[C/T]TGAGTACTGAGTCCC | 11124 |
rs182504681 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50718295 | AGCCTCCCAAAGTGT[G/T]GGGATTACAGGCATG | 11124 |
rs182504910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50763682 | TATTCACTGACCTTT[C/T]CAACAGTTAAACTGT | 11124 |
rs182507270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452306 | ATTCATAAGTGAAGA[C/T]TCTGTAGTGTGGCAA | 11124 |
rs182508417 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50870855 | CAAGTCATGTTTCTC[A/C]TTTTAAATCAAAAGC | 11124 |
rs182510730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50783356 | TCCTAACTTCTTTCA[C/T]GAGGCCAGCATTACA | 11124 |
rs182510907 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50738222 | GCCGAGGTGGGCAGA[C/T]CACCTAAGGTCAGGA | 11124 |
rs182512998 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50756460 | TTCAACAAGTCTCCA[A/G]GAGGTTCCAAACTTT | 11124 |
rs182514600 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50807235 | ACAATTTTAAAACAC[A/G]GTCACAGGTGTATTA | 11124 |
rs182516858 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50922698 | TGGTGCATACCTATA[A/C]TCCCAGCTACTTGTG | 11124 |
rs182521168 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50473405 | TTAAAGATGAGACCC[A/G]TTCAGAAAGGGAGTG | 11124 |
rs182522766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905156 | TTTTACTGTATTTGC[A/G]ATCGTTTGCTCAGAA | 11124 |
rs182525176 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50905336 | ATTGTGAATAGTGCC[A/G]CAATAAACATGTGTG | 11124 |
rs182528712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50887207 | CTGTTCACATCCTTC[A/G]CCCACTTGTTGATGG | 11124 |
rs182533060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465884 | ACATGTTTCATGGTG[G/T]TGTACAAATAGCAAA | 11124 |
rs182533236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50871441 | TCAAAGGGCAGGCTG[A/G]CTTTCTCATTAGGGG | 11124 |
rs182539082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872236 | GTCAAAATATCAACA[A/T]CAACAAGAGTTTGGG | 11124 |
rs182539840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849340 | TGTATTTATAAGATG[C/T]TAACATTAGCAGAAG | 11124 |
rs182543734 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50544187 | TCCCATATGAGTTTC[G/T]GTGGGGATGCTCAAA | 11124 |
rs182550230 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519523 | GCTACAATTTTTGAT[A/T]GGGGCGTTTTGCCTA | 11124 |
rs182557542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497137 | CTTAAAGTTAATAAT[A/T]AAAAAAAATCTGAAA | 11124 |
rs182558042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543692 | CAGGCCAGCTCTATG[A/G]GACTTTATTTTGCAC | 11124 |
rs182564535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588240 | TGCAGTACGTGCCAC[C/T]ACATCCAGCTAATTT | 11124 |
rs182567896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608191 | TGGGTTGTTTAGTTG[C/T]TGACATGGAAAGGGG | 11124 |
rs182573660 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50495940 | ATAGTCCTCTATCTC[C/T]GAGACAATAGCCATT | 11124 |
rs182574222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50567425 | TTTCTTACACTTTAA[A/C]AAGGCTGGGATGATT | 11124 |
rs182601963 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50725575 | ATTCCCGTGCCTCAG[A/C]TATACGAGTAGCTGG | 11124 |
rs182630433 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50654494 | GAAAACAGCAATGAG[C/T]GGAAATGACAGAGAT | 11124 |
rs182643345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50693693 | CAACAGAAAACGCTA[C/T]TTCAACCCTGAGCCC | 11124 |
rs182649095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50697483 | TTCTGATTGATCCTA[C/T]GTCTGTCTGTTTTGG | 11124 |
rs182657484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50733339 | CTCCATCTGTCTCCA[A/G]TCTTCTATTATTACA | 11124 |
rs182659179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736870 | AAGGTTCTGCATGGA[A/T]TTTGTTTTGTTTTTT | 11124 |
rs182663839 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803355 | GAAGAATACTAAGGA[C/T]TCAGAAAGTCTAAAG | 11124 |
rs182665612 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769449 | ACTCATTTTATGAGG[C/T]CAGCATCATCCTGAC | 11124 |
rs182694034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50664627 | AAACCTGTCTCTACT[A/G]AAAATACAAAAACAA | 11124 |
rs182710062 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645229 | AAAGATTGCCTGAAT[C/T]TGTCTGCCCTAGGAC | 11124 |
rs182730713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50917831 | TAAGTCACACACTGG[A/G]AGAAAATGTTCGCAA | 11124 |
rs182742536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50477708 | TACAGCATTCACTAT[G/T]TAGTACCATAGTTAT | 11124 |
rs182743567 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50949286 | ATTCTGATGCAAACT[A/C/G]AAGTTTGAGAACCAT | 11124 |
rs182745606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50900931 | GTTACAATTTAAAGA[C/T]TTGATCTTGATGTGA | 11124 |
rs182750011 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885054 | TTGTCAATTTATTGG[A/C]ATATAGTTGCTCTGA | 11124 |
rs182759774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945004 | TAAGTAAGGTGTGTG[A/G]ATCAAGAGGAGGTGA | 11124 |
rs182760372 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50868753 | TGTAATTTAATTCCA[C/T]TGTGGATGGAGAACT | 11124 |
rs182769634 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847526 | TTGAAGATAGATCTA[C/T]AGAAATTACTAGAGC | 11124 |
rs182780744 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50913272 | AAGGATGAATGGATC[A/G]ACTTTATACAAATAC | 11124 |
rs182782700 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50887637 | TATTAAACAGGGAAT[A/C]CTTTCCCCATTTCTT | 11124 |
rs182784281 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50500277 | TTTATTACAAAGCTG[A/C]AGTAATAGTAATTCT | 11124 |
rs182787876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50817294 | TATCCATACAATGGA[A/G]TATTATTCAGCGTTA | 11124 |
rs182790321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881891 | TATGTGCATTGAAAA[C/G]ATATACAGGTAAAGC | 11124 |
rs182793035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50447635 | CAACCCTTTGCCACG[C/T]TGGCAGAAAATCTGT | 11124 |
rs182796875 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50836182 | TCTGTTTTTTTTTTT[C/T]TTTTTTTAGACAGGG | 11124 |
rs182800702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469464 | ATTGTGGTTTAATGA[C/T]GAGATGCATGTGCTG | 11124 |
rs182806355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844163 | CATGTACCTGTTGAC[A/C]ATCTGTATGTCATCT | 11124 |
rs182813651 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50926413 | ATACAACTGTAGATA[C/T]TGGAGACTGGGAAGG | 11124 |
rs182821442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850146 | AAAAAAAAAAAATTG[A/G]ATGGTCAACAAGAAA | 11124 |
rs182822150 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50945138 | AGCATCAAATACCTT[C/G]ACAATCAGTTCATTG | 11124 |
rs182831423 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50909458 | TCTCCTGGGTAATAT[C/T]CTTTAGAGTGTTTTC | 11124 |
rs182832986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50891703 | CAAATGTTGCTGCCT[G/T]ATGATTCCTCTTGAA | 11124 |
rs182836052 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50487004 | GATGATTTTACTATA[G/T]TGTACTTTAGCCTTA | 11124 |
rs182840006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516855 | CACAAACACTTTGGA[C/T]TGGTTGCAAAGTTGA | 11124 |
rs182845800 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50877129 | TTCCTTCCCAAGGGC[A/G]ACAGCACAGGTAGTG | 11124 |
rs182850628 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50443326 | TAAACCACACCCAGT[A/T]TTCATATGAGAAAGC | 11124 |
rs182855049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50857382 | CCAATACTGCTCCAA[C/T]GCCATTATACAATCC | 11124 |
rs182860886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50670951 | AAATAAATAAAGTAG[C/T]TTGATAAGTATCAAT | 11124 |
rs182868403 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50707019 | CCATCCTGGCTAACA[A/C]GGTAAAACCCCGTCT | 11124 |
rs182873684 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50566717 | GTTATTAAAAAATAA[A/C]CTTACTACTAGGATT | 11124 |
rs182874665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689385 | GTCAGGAGATACAGA[A/C]CATCCTCGCTAACAC | 11124 |
rs182876127 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50649004 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT | 11124 |
rs182880654 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50621956 | GGATGGCCTGAGGTC[A/G]GAAGTTCGAGACCAG | 11124 |
rs182914214 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50688903 | AAAACAGTAAGCTGA[A/G]TGAAATAAGCCAAAT | 11124 |
rs182919248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50680909 | GAACACTGAAGCATA[A/G]AATTTAAGCAAACCA | 11124 |
rs182929981 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50718064 | TCGCTTTGTCACCCA[C/G]GCTGGAGTGCAATGG | 11124 |
rs182947373 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50726615 | TGGGCGGATCACAAG[C/G]TCAGGAGATTGAGAC | 11124 |
rs182950733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50755928 | ACACAGCACAGGGAC[C/T]CTGGGTCCAGCCCAC | 11124 |
rs182972876 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50797853 | AAAAATAAATAAATA[A/T]AAAAATAACACCGAT | 11124 |
rs182985092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760151 | ACTATCCTAAATATA[C/T]ATGCACCCAATACAG | 11124 |
rs182996830 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50779031 | TCACATTCTAAATCC[A/T]TTTTTTGTCATTTCA | 11124 |
rs182999698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50798825 | AAGCTGTGGAAGACA[G/T]ACATTATGTACATGT | 11124 |
rs183002236 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50804264 | ATGTCCAAAAAGTAA[A/C]TGAAAAATCACAGCT | 11124 |
rs183005783 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FAF1 | GRCh38.p7 | 1:50826952 | GTGCCCGGCCGCCCC[A/G]TCTGGGAGGTGAGGA | 11124 |
rs183008292 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | FAF1 | GRCh38.p7 | 1:50820545 | TAGCAAATTTCGAGA[C/G/T]GTAAACAATATAGTA | 11124 |
rs183021226 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50834853 | AACAAATAGTTATAA[C/T]GTAGTTCTATAACAG | 11124 |
rs183039289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50539949 | CCCTAAATGCTGTCT[A/G]GGGCTGACAGCATAG | 11124 |
rs183045944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50593322 | CCCAAATAACACATA[C/T]AATAGTGAGGGTGAG | 11124 |
rs183050672 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50513429 | TGGGAGGCGGAGGTT[G/T]CAGTGAGATGAGATC | 11124 |
rs183055155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50492578 | TAGCCAATATACATA[C/T]ACTTAGCTTTAATAA | 11124 |
rs183058555 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50635573 | TGCGACCACGGGTGC[A/G]TGCCACTATACCCAA | 11124 |
rs183063061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50952108 | CTCTCCCCTTTCTAC[A/G]GTCTCCATCTCCCTC | 11124 |
rs183066912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50653913 | CCTCAGGTAATCCAC[C/T]GGCTTCGGCCTCCCA | 11124 |
rs183068660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895863 | ATGATTTTAAAAAAA[A/C]AGCCTCAACACACTG | 11124 |
rs183075477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50563261 | ATCAGAACTACTGGT[C/T]AAACCAATATTTAAG | 11124 |
rs183075478 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50615140 | AGAACACACAGTGTT[C/T]GGTTGTCTGTTCGTG | 11124 |
rs183081143 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50674995 | TCCTGGGTTCAACCA[A/G]TTCTCCTGTCTCAGC | 11124 |
rs183087980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875918 | TTTAACTATCACTAC[C/T]ATCCTTTTCCTCAAA | 11124 |
rs183088156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863339 | AATGGCACAACCTAT[C/G]AAAACCTCTGGGATA | 11124 |
rs183093420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50692312 | GGAACATTTAAATTC[C/T]AATCTTTTAGCAATT | 11124 |
rs183094204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50856453 | TGCTTTGTTGGAGTA[C/T]AGCAACAATGGTTAA | 11124 |
rs183098322 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50731562 | TTTAGTAGAGACGGG[A/G]TTTCACTATGTTAGC | 11124 |
rs183101961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50838913 | ACACTGGAAGCTGAA[C/T]ATATGTTTCCAGTAT | 11124 |
rs183102392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562478 | ATGCCCTTTAGTAAA[A/G]AAGAGCAAAATCTGC | 11124 |
rs183106820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50711305 | TACTTTAAAATCTTA[C/T]AGTGATAGTGAAACA | 11124 |
rs183109570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50501917 | GTACACAAATGTTCA[C/T]AGCAGCTTTATTTGT | 11124 |
rs183120152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479297 | GCTGCCTAGTCAGTT[C/T]TGATGAGAGAACCTG | 11124 |
rs183120202 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50539180 | GAAACAATTGTCACT[G/T]TGAAAAATTCAATCT | 11124 |
rs183124330 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50855469 | ATATAAAATACAGAC[A/C]TATCCGAGGTTACAA | 11124 |
rs183132181 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50458545 | GTAAGGGCAAAATTT[G/T]TAAGGCTCTGAATTC | 11124 |
rs183132808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562747 | GATTGTGTCTTGTTC[C/T]ACCTTTCATTCTCAG | 11124 |
rs183138819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50625047 | GCTGGGATTACAGGC[A/G]TGCACCACCACGCCC | 11124 |
rs183145430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50513121 | GCTCTGAAATGTACT[A/G]AGCGTTTCCAGGCTG | 11124 |
rs183148546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50584043 | TGAAATAGACATCTT[A/G]TGACTAAATTATATT | 11124 |
rs183150974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559830 | CTTCATTTTAAAGCA[C/T]TAATTAAGCCCTTGA | 11124 |
rs183151819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50524877 | ATTCAGGCTCTTTTT[C/T]TTGGTCCCATATGAA | 11124 |
rs183151838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602852 | CCATGAAACCATTCC[A/G]TATTTTAAAAAGCAG | 11124 |
rs183156655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603118 | AAAAGTATCCAATCG[A/G]ACAACTATTAAGGCT | 11124 |
rs183175965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50600026 | AGATTTTCAGATTAC[A/G]GATACTCAACCTGTG | 11124 |
rs183189207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50629726 | ATGTGGGGATAATAA[C/T]ATCTACCCTTCGGGA | 11124 |
rs183206764 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50670366 | GTGCTGGGATTACAG[A/G]TGTGAGCCACGGCGC | 11124 |
rs183220734 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50706122 | AATTTCAAGTCTAAA[C/T]GCTTTGTATACTTAA | 11124 |
rs183229989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50747773 | AGTGGGGTCTGGTAG[A/G]AGGTGACTGAATCAT | 11124 |
rs183266050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775056 | AGGTGCATAATCTGA[C/T]TGAGCATCTCTTTGC | 11124 |
rs183283819 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50816665 | ATAGCTTCTTTTGCT[C/T]GGCAGAAGCTCTTTA | 11124 |
rs183287697 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748018 | TGCGAACCAATTAAA[A/C/T]CTTTTTTCTTTATAA | 11124 |
rs183298524 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50785388 | CATATATCTAATAAG[C/G]GGTTAAAATACAAAA | 11124 |
rs183310347 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50824945 | GAGGGATAGGGGAGG[G/T]TGGGAAGGGTAGGAG | 11124 |
rs183320188 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50936216 | AACATATACTTCCTG[G/T]CTGTAAAGAACTCAC | 11124 |
rs183321253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50692644 | TAGTATTCTGTTGTA[C/T]ATATTCATATATACC | 11124 |
rs183333710 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50456595 | CAAAAATAGTGGATG[A/G]ATAGCTGGGAACATT | 11124 |
rs183334777 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50712714 | ACATTTTTGCTAAAA[A/T]GTTATCTAGGCAAAC | 11124 |
rs183337163 | snp | A/G | 0.113685 | 0.209567 | intron-variant | FAF1 | GRCh38.p7 | 1:50929086 | CAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 11124 |
rs183341152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50442485 | TCTTGCCCAGAACAG[A/G]TGTTCCATAATGACT | 11124 |
rs183341176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948659 | CGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 11124 |
rs183342093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50732986 | TAATCAGTATTTCTA[C/G]CCTTCTTCAACTGTA | 11124 |
rs183343088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50752350 | TTTTTACTTCTGTGA[A/C]TGTGGTAACTTGTAC | 11124 |
rs183348397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912332 | CAGACTACTGAATCA[A/G]ACTTTCTAGAAGTAG | 11124 |
rs183354284 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50873013 | ATTTTAAGAAATTGC[C/T]AGAGCCACCCCAACT | 11124 |
rs183357533 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768804 | TAAGAGAAAAGTTTA[A/T]AACACTAAATGTCCA | 11124 |
rs183362838 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50791914 | TTCAAGGACAAGATT[C/T]AAGAATTGGCTTGAT | 11124 |
rs183363072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50850374 | AATCCAGTAACAGAG[A/G]CCTTTAAAGAACAAT | 11124 |
rs183363091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50895318 | AGACTGAACCCTGGG[A/G]AAATCCAAAATGTGA | 11124 |
rs183365546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50881382 | CTGGAAGGCTACTTT[C/T]AAAGTTGTCCTCCTG | 11124 |
rs183367017 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50811458 | CAATTCCACTTACAA[C/T]AGCCACAAAGAAAAT | 11124 |
rs183370161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50492325 | AAATACTCTGGTTAA[C/T]CTCATTCCATACCAC | 11124 |
rs183372107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50934952 | GTTTTAAAGATTTTT[C/T]TCTTTATCTTTGGTT | 11124 |
rs183374271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50506787 | AGATGACAGAAAAGA[A/G]GAAAGAAAAGAAGTG | 11124 |
rs183375971 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50828667 | ACAAAATTAACTTTC[C/G]ATAAATTACGACATT | 11124 |
rs183380537 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50875595 | GCAGCTGAGATTACA[A/G]GCACTTGCCACCATG | 11124 |
rs183382795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863035 | AGACATTTACAGAAC[A/C]TTCTACCCAACAACT | 11124 |
rs183386475 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50486435 | CTTCCCTTTGGTGTC[C/T]ATCCAACCATCCATC | 11124 |
rs183396548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465157 | GCCACTGCTTGGCTA[C/T]GTGATCTTGGTTAAA | 11124 |
rs183396895 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50838572 | AAATATATATATTTT[A/G]TATAATTATAAAAAT | 11124 |
rs183399312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50557224 | GTATTGAGGGGAAGA[A/G]AAGCACATGAAAGCA | 11124 |
rs183401873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50839341 | AGTTCACATACTCCC[A/G]CTAAAAATTCACAAT | 11124 |
rs183404566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50539496 | TTTTCAAATGCAAAG[A/G]TATTTACTAATAGAA | 11124 |
rs183407665 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50868334 | CTATTGAAATTTTTT[A/T]AAAAAGATAAAATAA | 11124 |
rs183416312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50530777 | ACCTACTGTGTACCC[A/C]AAAAATGAAACAAAC | 11124 |
rs183420966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50500525 | CAAAATTTAACTGAA[A/G]TGGATCATAGACCAA | 11124 |
rs183428279 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457423 | GAAAAGGTTAATCTG[C/T]GCACATACACATTTG | 11124 |
rs183436561 | snp | C/G/T | 0.000650368 | 0.0180214 | intron-variant | FAF1 | GRCh38.p7 | 1:50584664 | TTCTATTGCTGGACC[C/G/T]AAAGAGCTATTAATA | 11124 |
rs183454457 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50625221 | CCTACACTCTTAACA[A/G]CAATACAGGGAATCC | 11124 |
rs183454687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550185 | TGAAACCCCTCTCTA[C/T]TAAAAATACAAAAAA | 11124 |
rs183488860 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50727414 | TCTGGTCAATCAAAA[G/T]AAATCAAAGCTAAGG | 11124 |
rs183494741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50665543 | AAGCAGAGCCCAGAG[C/G]TCAAATCCAGTCTAC | 11124 |
rs183501234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625820 | GGCAACGGGAAACCA[C/G]TGAGAGATTTGAAGC | 11124 |
rs183501635 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50764222 | CTCAGTTTTAATTAC[C/T]AATATGGAAAATATT | 11124 |
rs183522125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50958338 | CAGATTTCACTGGGT[A/G]ACCAAAACAGCAAAC | 11124 |
rs183532177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50704025 | CTACTTTATAATCAC[C/T]GAACATTAATGAATA | 11124 |
rs183532828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943797 | GTAGAGGAAGGTCCA[A/T]GTTTCTAGGAGGGAG | 11124 |
rs183538149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50743782 | TCTGGAAGAAAAAAA[A/G]GTGTGTAAGCCCAGG | 11124 |
rs183538939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50589559 | GTTTTAGGAGTTCTC[C/T]ATATTTTATAGACAT | 11124 |
rs183542449 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808168 | ACTAAAATAAGCTTC[A/G]TAAGAAAAGGATAAA | 11124 |
rs183550995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50630014 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 11124 |
rs183554363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649912 | GGAGGTTGCAGTGAG[C/T]CAAGACCATGCCATT | 11124 |
rs183569781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50831080 | AAAGAAACCATAGTA[C/T]ATAGAAAAATTCAAC | 11124 |
rs183596912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951500 | GAAACTGAGGCAGAG[A/G]GGTGTGAGGTGATTG | 11124 |
rs183600075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454162 | TAAATTTTCGAACAG[C/G]GGGTAGGGGCTTGGC | 11124 |
rs183604518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50917459 | TTTGCAGCAATCAGA[A/G]GGCCTCAAACATAAT | 11124 |
rs183618604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50948935 | ACCCCCATGATCCAA[C/T]ATCTACCTCTAGGAC | 11124 |
rs183624260 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50520986 | TTCTCCAACTTTAGA[C/T]GACAAATTCCTTAAA | 11124 |
rs183625117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667261 | TATACACTTTTGGCC[A/G]ATGCCTTCTGAGTCT | 11124 |
rs183628418 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | FAF1 | GRCh38.p7 | 1:50884510 | CTGGGCCACAGAGTG[A/T]GACTCTGTCTCAAAA | 11124 |
rs183630453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50497783 | TTGAACTCCTGGGCT[C/T]GTGATCCACCTGCCT | 11124 |
rs183636480 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50474417 | AGTTTGTTTTTTTTT[A/T]AAATTTTTTATTTCC | 11124 |
rs183641753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50524148 | TCTCTAATGACCTGT[C/G]ATGCTGTGATTTTTA | 11124 |
rs183642175 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50446952 | GTGGTAGAGGCAGAA[A/C/T]CAGAACCCAGGCCTT | 11124 |
rs183648100 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50686772 | AACACCTAGGCAATA[C/T]GACAAAAAGAGTTCT | 11124 |
rs183652952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50724732 | CTTACAAGGTCATAC[A/G]TACCACGTTAGATTT | 11124 |
rs183656423 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50847164 | CACCTGGGATTGTGA[A/G]TTAGTCATTCAGACT | 11124 |
rs183664158 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50704863 | TAAAAAAGGAAACCA[C/T]TAATAGTCTACAGAA | 11124 |
rs183668446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50491155 | AGTCCCACTCCCTGG[C/G]TCTCCAAAAAAAACC | 11124 |
rs183673822 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50745520 | GGATCATAGGGGGCT[G/T]ATTTCCCTCTTTGAT | 11124 |
rs183676035 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50478803 | TTCAAAATTTGAGTC[A/G]GTGTTGTATTGTATA | 11124 |
rs183677096 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50762263 | AAAATGGCCATACTG[A/C]CCAATATAATTTATA | 11124 |
rs183679269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779901 | CAGCCTGGGCCGCTT[A/G]GTGAGAGCCTGTCTC | 11124 |
rs183688814 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573711 | TGGTGTCTTTTTCCC[C/G]TCACTTTCTGAGCAG | 11124 |
rs183690639 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50806112 | AAAAGTATTTATAAT[A/C]CATGTATCTGAGATA | 11124 |
rs183708562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603364 | TCAGGTACCAGATGG[C/T]AAACCAGATTTAACT | 11124 |
rs183715656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896582 | GGAATATATGTGCAA[C/T]AGAATATCACTCATC | 11124 |
rs183718339 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50573956 | AACAGGGCGAAACCC[C/T]ATCTCTACTAAAAAT | 11124 |
rs183727236 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645785 | GTGAGCTGAGATCAC[A/G]CCACTGCAGTCCAGC | 11124 |
rs183729084 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50882646 | AATAAATAAATAAAT[A/G]AATGTGTATGTATGT | 11124 |
rs183735346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863696 | CTGCCCGGCTTTGCT[A/G]TCAGGATGATGCTGG | 11124 |
rs183737886 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50953461 | AAAATTTGGCCAGAC[A/G]CAGTGGCTCACAGCG | 11124 |
rs183742607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50844667 | ATGAATACAAAGAAT[C/T]TGGAAGATAATGTGA | 11124 |
rs183752578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685732 | TCAAATGAACTAAGG[C/T]TGGAGAAATGAGTTG | 11124 |
rs183760177 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751700 | ATGTATACTATAAAC[A/G/T]TATTTATACATTTTA | 11124 |
rs183762102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722591 | GCGGCAGAGCTTGCA[A/G]TGAGCTGAGATCGCG | 11124 |
rs183775834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836922 | CTTCCAACTCTTCCA[A/T]TTGTCTCTTACAAGT | 11124 |
rs183788823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50789902 | ACCTTAATCATTCCC[A/G]TTTCACAGAGGAACA | 11124 |
rs183791538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810814 | AGCACTCTGGGAGGC[C/T]GAGATGGGTGTATCA | 11124 |
rs183791905 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50615531 | ATGCAGTCTTGCCAG[A/C]ATCTACTGTTTTCTG | 11124 |
rs183807448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50873969 | CTTCAGCCCCTAGTA[G/T]CTACATCCAGTTGAG | 11124 |
rs183809502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50654348 | ACTTGAGATTTCCAG[A/T]AACATTCTCATTTTT | 11124 |
rs183811310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851241 | ATGCGCCACCAAGCG[C/G]GGCTAATTTTTGTAT | 11124 |
rs183842653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581803 | AGAGTAAGATTATGG[G/T]GCAATACAAATGGTA | 11124 |
rs183849630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601635 | TGCAGTGAGCTGAGA[C/T]TGAGCCGCTGCACTC | 11124 |
rs183854051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50561378 | GCTTTAGTACCATAT[A/G]TTAGTACCATTAGTG | 11124 |
rs183859240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930348 | TTAGGGTACAGTACT[A/G]TTCAGGAAGGTATAT | 11124 |
rs183865798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469194 | ATCCAGGACCAGTTT[C/T]CTTTACAACAAAACT | 11124 |
rs183865825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50925847 | GGAGTCAGCCTAAAT[A/G]TCCATCAACAGGCAA | 11124 |
rs183868542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50869353 | TAAAGTACTTATATT[C/T]CATGTAATTATTATG | 11124 |
rs183869249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50498200 | GTTAGGAAAGCTGGA[C/T]ATCCACATGCAAAAG | 11124 |
rs183870033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50643396 | AAAAATTCCATATTG[C/T]TTATTAATTTTTTTC | 11124 |
rs183872871 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50891289 | AGGTTTTTAACTTCT[G/T]TGAGATGGGTTCGAA | 11124 |
rs183874349 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50760982 | aagaatcaaataaat[C/G]caataaaaaatgata | 11124 |
rs183880005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50474856 | CTTGGTTCCCTACAA[A/G]GAAATGGTGGTTAAC | 11124 |
rs183885420 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50682953 | AAAATTAGCTGCTTG[A/C]ACCTGGCAGGTGCAG | 11124 |
rs183891530 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50804821 | GATAAAATTGAAAGT[C/T]TGGTTAAATACAACA | 11124 |
rs183893736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570150 | GAATAAGCCTCTAGC[C/T]CCTAGAGAGACAGCT | 11124 |
rs183894223 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50662335 | GAATTCTTCATTCTA[A/G]TAACTGTAACTTAGT | 11124 |
rs183898109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50546205 | AAAATTATAGTATAT[G/T]ATGGAATTTAAAGAG | 11124 |
rs183906603 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50521178 | GCTTTTTATGGTGAG[A/G]ACTCACACTATTTTT | 11124 |
rs183914988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50611986 | ATTCAACAGAAGAAA[C/T]TGCTTGTTTGTAGAA | 11124 |
rs183921634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50633148 | GAACTGAAAGATAAT[C/T]TCTGCACTTTGGATG | 11124 |
rs183921688 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50591213 | ATTCTGTAAATGTGC[C/T]GTATTACATTGAGGA | 11124 |
rs183930304 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50512196 | TGTAGGTTGCCTGTT[C/T]ATTCTGATGATAGGT | 11124 |
rs183931969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50956189 | TTTTTCATTAACAGA[C/T]TGGGGGAGGATTTTC | 11124 |
rs183944523 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50550635 | AAAGGAGTATTTAAG[A/G]ACCACATCACCTAAA | 11124 |
rs183954669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50887973 | TTACCTTGGGCAGTA[C/T]GGCCATTTTCACGAT | 11124 |
rs183960404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893256 | TATGGATGTTTGCTG[G/T]TGTCTGGGCATATAT | 11124 |
rs183963257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50878916 | TCCCCCACAGCTCTG[C/T]CTCTCTTGTTAAATG | 11124 |
rs183965212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636195 | AGTAAAATGCACCCA[C/T]TTTAAAGCATATTTA | 11124 |
rs183970298 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50859446 | TACAAAAATCAGTAG[C/T]ATTTCTACACACCAA | 11124 |
rs183974357 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50594586 | AGGCTTGGGCCAGGC[A/G]TGGTGGCTCACACCT | 11124 |
rs183995904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938765 | CATATATGGTGAAAG[C/G]TAAGGGTCTAGTTTC | 11124 |
rs184006955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50676330 | GAGAATTGCTTGAAC[C/T]CAGGAGGTGGAGGTT | 11124 |
rs184016364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50946052 | CAGACAGTGAAGTGG[G/T]AACTAAAGTTTCCTC | 11124 |
rs184020444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50920784 | GCAGAAGGACATCTA[C/T]GAAAAACCTATAGCT | 11124 |
rs184024713 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50903408 | AGTCTCCTCAAGATA[C/T]GACTGGTGTCTTGTC | 11124 |
rs184030360 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50520697 | ACTAAAAATACAAAA[A/T]ATTAGCTAGGTGTGG | 11124 |
rs184031000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886281 | TCTGGTGTTGATGAA[A/T]TCCCTCCGCTTTTCT | 11124 |
rs184034041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869998 | CATTATGATGGTATC[C/T]TTATAAAGTGTTTCC | 11124 |
rs184044522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744324 | CATGTGACTTCTTTC[A/G]GACCAATATGTAATT | 11124 |
rs184045035 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50443836 | CTGCAGCTCTTTCAC[C/T]AAAACCTCCTGGAAC | 11124 |
rs184047438 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50473839 | GTCTCTATCCTGCAA[A/C]CCTGACAGCCAATGT | 11124 |
rs184051252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50848485 | TCATTGGCAAAAGTT[C/T]AATAAGAAACAGGAT | 11124 |
rs184053619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779575 | GATATGAGATAAATA[C/T]AGAAAATTATATATA | 11124 |
rs184063452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639883 | AGGTTGCAGTGAGCC[A/G]AAATCATGCCACTGC | 11124 |
rs184066393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50599206 | CAACCTCCACCTCCC[A/T]GGTTCGAGTGATTCT | 11124 |
rs184069837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50821269 | TCTGCCTCACACTGG[G/T]CTAGAAATTCAGTTA | 11124 |
rs184071860 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50567795 | AGCCCTTATTTATCA[A/G]CATGTGACATGTAAT | 11124 |
rs184095016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941190 | GGTGCGCGCTGCCAC[A/G]CTCAACTTTTTGTTT | 11124 |
rs184097050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50679817 | ACTAAAACATAAATC[A/G]CTTCTGTACATGCAT | 11124 |
rs184099836 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449201 | ATATATTATCTAAAC[A/C/G]TTAAAGCTATCCTAA | 11124 |
rs184105206 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50503213 | TAACACTGTTAATAA[A/T]TGCTAAATGGTAGTT | 11124 |
rs184112992 | snp | A/T | 0.0821764 | 0.185298 | intron-variant | FAF1 | GRCh38.p7 | 1:50905937 | CTTTTGGTGTTTTAG[A/T]CATGAAGTCCTTGCC | 11124 |
rs184122432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50647375 | GCTGTTTCTGTACCT[C/T]GCTTCTTTCTGTACG | 11124 |
rs184126618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50574341 | CAGAGAAGCAGGCAT[A/G]CTCTTTGGGGAGGCT | 11124 |
rs184128484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551561 | GAAAGATGGTTTATG[A/G]ACAATTAGAATACAG | 11124 |
rs184130322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50605748 | AAGAAGGGTGAGGGG[G/T]AAAGAGAGATCTGGA | 11124 |
rs184131335 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50494513 | ACAGGTCTTACGTGT[G/T]GCCTAGGCTATGGCT | 11124 |
rs184135356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526191 | TAGAGATAGGGTTTT[A/G]CCATGTTGCCTAGGC | 11124 |
rs184142872 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50616217 | CATTGGTCTATGTGT[A/C]TGTTTTTGTATCAAT | 11124 |
rs184144859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471364 | ATTTGTATACCCCAA[A/G]TTTGAAAGGCTTTTC | 11124 |
rs184158376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50699451 | TAAGATTATTAATTA[C/T]ACAACTGCAATTCAC | 11124 |
rs184161507 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50662848 | TGGGACTGCAGGCAC[C/T]CACTAGCGCGCCCGG | 11124 |
rs184166274 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50843502 | CCTTCTATCTACTTT[G/T]GTACACATAAACCAA | 11124 |
rs184168399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50595231 | AACTAATTTTGTATT[G/T]TTAGTAGAGACGGAG | 11124 |
rs184170071 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50612509 | TGTATGCATGAAGGG[C/T]ACCAACGAGCCACTT | 11124 |
rs184174753 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50683162 | GAAAAACAGTATTTT[A/T]AAAAAAAACATATAT | 11124 |
rs184177410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50720158 | AGGCATGCACCACCA[C/T]ACCCAGCTAATTTTT | 11124 |
rs184182555 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50577992 | CAGTTTTCATTAAGA[C/T]GGATTGAATGTGGCA | 11124 |
rs184187952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497636 | TCATTGCAACCTCCA[A/C]CCCCCCAGGTTTAAG | 11124 |
rs184188818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50787440 | CCCTTTTGCCCTTCT[C/G]GTTTCTGTCATGTGA | 11124 |
rs184189092 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50453327 | ATCCAAGCAGGGCCA[C/T]GCGAGCTGGTGTGTG | 11124 |
rs184193694 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50757618 | AGTTCTTTTCATTTT[C/T]AGTTTTTATTCAATT | 11124 |
rs184193875 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | FAF1 | GRCh38.p7 | 1:50740024 | AAGCCAGGAAATGCA[C/T]TTATCAACAGATATT | 11124 |
rs184200175 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50634148 | GCTACTTACCATGCA[A/T]AAATGTTCATTTTCA | 11124 |
rs184200728 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50754810 | AATCATGGTGGAAGG[A/C]AAGGAGGAGCAAGTC | 11124 |
rs184201140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50808987 | CACCCAGATTCAAAC[A/G]GCAAATACTTAGAGA | 11124 |
rs184202168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620391 | GAAATTCTTGTAGTA[A/C]ACTTAGCAGCTCTAG | 11124 |
rs184203520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50673014 | TATAATCCCAGCACA[C/T]TGGGAGGCTGAAGCA | 11124 |
rs184206917 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | FAF1 | GRCh38.p7 | 1:50827171 | CATGATGACGATGGC[A/G]GTTTTGTCAAAAAGA | 11124 |
rs184208729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652863 | ATTATAATGTCGACT[C/T]ATTTACTGAGTGTCT | 11124 |
rs184209086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50777303 | GTGCGCCTGTAGTCC[C/T]AGCACTCGGGAAGCT | 11124 |
rs184212203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709528 | CCTGAGGTTTCATTT[C/T]ACTCACAAAATTATA | 11124 |
rs184214245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906789 | TTTGGGCTGAGACGA[C/T]GGGGTTTTCTAAATA | 11124 |
rs184214692 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50690668 | GAAGAAGTTTAATAT[C/T]TAAAATGCATTGTGC | 11124 |
rs184215775 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50821946 | TCACCGAAATGCTCT[A/G]TTGATTACAGATAAG | 11124 |
rs184217751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50738548 | TAGCAATGAGAGAGA[C/T]TGGAACTCCATTTAT | 11124 |
rs184219285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545084 | AAGATAAATAACAAA[C/T]GGGGAAATTTTCTGA | 11124 |
rs184220815 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50795469 | GTGTATGCCATTACC[G/T]AGGAGCAGCTAGCTT | 11124 |
rs184221722 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729042 | TATCTATCTATATAT[A/C]TATATATATATATAT | 11124 |
rs184223295 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50756526 | CTATTCCAAACTCTG[A/C]GTGTTACCCAGTTCC | 11124 |
rs184224806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50776028 | AGCAGGTAGATATCA[A/T]ATAATAACAATATCT | 11124 |
rs184237137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50799343 | TGAGTATTAAATGAA[C/G]AAAAATATGTCAATT | 11124 |
rs184238950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50696147 | ATCTTATTTTGAACA[C/T]TGCCTAGCTCTCTCA | 11124 |
rs184243492 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874292 | TAATTTCTTAAACAT[A/C]AAAATAAAACCATCC | 11124 |
rs184243664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50659130 | AGGAAACCTCAATGA[C/T]AAAATACAGCTTTGT | 11124 |
rs184248723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50627781 | TACTTTTAAAAATTC[A/C]TCAAATTGTACATTC | 11124 |
rs184264017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50837107 | GGACTACAGGCACCC[A/G]CCACCATGCCCAGCT | 11124 |
rs184286551 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50848383 | TATTACCTAACTGTA[G/T]AATCTGTCTGATTAT | 11124 |
rs184328773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50735682 | AACTTAAGAGTGAGA[C/T]GGTTTGTCAGTGAAC | 11124 |
rs184347975 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50923845 | TTTTCATTTAAATAG[A/C]CATTGAAACAGCATT | 11124 |
rs184360559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50771868 | ATCGTGCCATTGCAC[A/G]CTAGCCTGGGTGATA | 11124 |
rs184378793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815058 | TTAAAAGCAGTCTCT[C/T]AAAAAGATATTTTAA | 11124 |
rs184380746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50888617 | TCAAAGGCCTTTTCT[G/T]CATCGATTAGGTTTT | 11124 |
rs184385482 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510674 | AAGAAAATACTTAAA[C/T]TGTAAACACATTTCA | 11124 |
rs184390989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50617062 | GTCCTTAGGGTTTTC[C/T]AGGTATAGAATCATA | 11124 |
rs184394621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468250 | CTGCATCACATTGTA[C/T]CCCATAACAATATAA | 11124 |
rs184396486 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661866 | GCCTTCTTTTCCTCT[C/T]GTTTTTAAAAGTATT | 11124 |
rs184399826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852091 | AAAAAAAGATTTGTA[C/T]GACATGCTTAGAAAA | 11124 |
rs184401955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632362 | AGTTTTCAACTGAAC[A/G]TCTAATTCAAGATAA | 11124 |
rs184403188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50656251 | GCAGGAGAATCGTTT[C/G]CATCCGGGAAGCGGA | 11124 |
rs184415011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638071 | TTTGGATAGAATTGC[A/G]AGTCATATAAGTTTT | 11124 |
rs184415514 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590454 | GCTTGTTGACTGTTG[A/G]TTTATAGAAATGCAA | 11124 |
rs184418584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927863 | TTCCTTGTGTCTCTA[C/T]GTGCCCTAATCTCCT | 11124 |
rs184420030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606464 | AGAGCATTTTTGTTT[A/G]GATATATTGTAGCTG | 11124 |
rs184423203 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947945 | AGCACCTTTTACTAG[A/G]TACTGTAGGAACAGA | 11124 |
rs184425448 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50672069 | TTTATTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 11124 |
rs184437429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50911589 | GTAGTCTCAGCTACT[C/T]GGGAGGCTGAGTCAT | 11124 |
rs184441224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50734181 | GCTTCCAATACTTCT[C/T]AAGTATCTTACCTTG | 11124 |
rs184442567 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714348 | TCTCTACTAAAAATT[A/T]AAAAAAAAAAAAAAA | 11124 |
rs184444369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50893496 | TGGATTAGCATATAG[A/G]AACTATTGTTATCTT | 11124 |
rs184446081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50879473 | TGAAAATAATTGCTA[C/T]AATATATGTTAAAAA | 11124 |
rs184458354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50753591 | AATGTCAGATCTGCT[A/G]TTAATCTCATCTGGT | 11124 |
rs184466882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50957628 | AAGTACTGGGATTAC[A/T]GGCCTGAGCCACCAT | 11124 |
rs184473208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50698808 | ATTTTATTTTAAATA[C/T]ATAAAAGGCATGCTA | 11124 |
rs184479502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739309 | ATGTGTACACGTACA[G/T]GCATATACATGTGTA | 11124 |
rs184487796 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50942921 | TACCTGACCTTTGCT[A/G]TGGAGGGAGAAAGTA | 11124 |
rs184496405 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50906343 | GTTCTTTTGGCTTAC[G/T]ATTGTCTTGGCAATG | 11124 |
rs184497299 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50448169 | GAAATAGCCATCAAG[A/G]GCCTGACACATGGAA | 11124 |
rs184498143 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50923278 | TTCCAAAAAAATTTA[G/T]CCAGGCAAAGGGGTG | 11124 |
rs184504954 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50777117 | TAATAATAAAAAATA[A/G]AATAAATAATATAGG | 11124 |
rs184505703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469914 | AATAACCAGATATAG[C/T]GACATAAAATAACTG | 11124 |
rs184506299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50535924 | GAAAAATGAGTCTTA[A/G]CTCAAAAAAACCTCT | 11124 |
rs184510722 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569200 | AAACCTTCCGTGATT[C/T]CCTCAGGCAGAGTTA | 11124 |
rs184510788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50946739 | AAGTATCAGCATGTT[A/C]TTGTGCTGGTTCTCC | 11124 |
rs184511407 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845985 | AAAAATTAGCTGGGC[A/C/G]TGGTGGGGCACGCCT | 11124 |
rs184513877 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50888227 | TTGCACATTGATTTT[C/G]TATCCTGAGACTTTG | 11124 |
rs184514713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50445178 | AGACTTTGGTGCACC[C/T]GTCACCCAGGCACTG | 11124 |
rs184521489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910911 | CCCCAGTGAGATGAA[A/C]CTGGTACCTCTGTTG | 11124 |
rs184521802 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50817583 | GGTTGCATAAAATTA[C/T]GAATATATTTAATGA | 11124 |
rs184548417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610201 | GCTCATTCAAATATA[G/T]GTATTACCTGTTTCA | 11124 |
rs184568608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650561 | GGAGGCAGAGGTTGC[A/G]GTCAGCTGAGATCTC | 11124 |
rs184599059 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50454861 | ATTCTGAGGGCACAT[A/G]AGAGATTTTACTGGC | 11124 |
rs184600795 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50487831 | AGAAGACAGGTAGTG[C/T]TGCTGTGAAAAGTCA | 11124 |
rs184612553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50719856 | TGAACTATCAATAGG[C/T]AATAAACTGTATAAA | 11124 |
rs184631301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50756844 | ACTTATTCACTATCA[C/T]GAGAACAGCATGGGA | 11124 |
rs184631594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50533566 | TTTAATGTAATACAG[C/T]GATAAATAAACTAAA | 11124 |
rs184641491 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50799772 | ATATATTCGACTTTA[C/T]TATAAAAACCAAACA | 11124 |
rs184653426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927439 | GACAAAAAATGAGCC[A/G]GGCATGGTGGCATGT | 11124 |
rs184697883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50780293 | CTGGGGAATTCATGT[A/G]GAGGTCAGAGTGGAA | 11124 |
rs184701141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806628 | GCACCACCCATGGAG[A/G]TGTCATGGCCAGAGG | 11124 |
rs184708837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822838 | GGAGTGCAATGGCAC[A/G]ATCTCAGCTCACTGC | 11124 |
rs184713112 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50690556 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 11124 |
rs184715047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50753991 | TCGATCTCCTGATCT[C/T]GTGATACGCCCACCT | 11124 |
rs184721257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734647 | GCTGAGGCAGGAGAA[G/T]GGCGTGAACCCAGGG | 11124 |
rs184721982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50651551 | AAATGACCTCACTTT[C/T]AATGACCTTTATAAC | 11124 |
rs184730760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771436 | GCAAAAAACAAACAA[C/T]CCCATTAAAAAGTAG | 11124 |
rs184731401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50840837 | ACTTATGGTAAAGAA[A/C]AATTACAGAGCCTAA | 11124 |
rs184732263 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50794868 | TCTTGAACTCCTGAC[C/T]TCAGGCGATCCACCC | 11124 |
rs184743798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50813710 | TCAAGTGACTCTCTC[A/G]CCTTGACCTCCCAAA | 11124 |
rs184749588 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50830508 | CAAATTGACCATTAG[A/T]TCAATACAGACTGAC | 11124 |
rs184766026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728747 | AATGAGCCGAGATTG[C/T]GCCACTGCACTCTAG | 11124 |
rs184773571 | snp | G/T | 0.151001 | 0.229563 | intron-variant | FAF1 | GRCh38.p7 | 1:50952944 | GATGGCGGTTTTGTC[G/T]AATAGAAAAGGGGGA | 11124 |
rs184775995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462897 | GAAGTGAATTTGAGA[C/T]ATGAATATCTTAAAA | 11124 |
rs184779189 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466722 | TTTATGTGGAATAAA[A/G]CCAAGCTCCTTCGCC | 11124 |
rs184780031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766079 | CCTGGGCGACAAGAA[C/T]GAAACTCTGTCTCAA | 11124 |
rs184785720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50483635 | GATTTATTAAGACTA[C/T]AGGAAAGGCAAAAAT | 11124 |
rs184788623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50508814 | TCAAGTGATTCTCTT[A/G]CCTCAGCTCCTGAGT | 11124 |
rs184793680 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863769 | ATTGGAATAGTTTCA[C/G]AAGGAATGGTACCAG | 11124 |
rs184810310 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50926985 | GTAACTTAAAAATAC[A/T]ATGTTAAGTGAAACA | 11124 |
rs184812096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50585895 | TAAAAAAAAAAAAAA[A/G]AAAAAAGAAAAAAGT | 11124 |
rs184816167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50800265 | AATTGGATGATATAT[C/T]CAATATGTACTCAGA | 11124 |
rs184820473 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50552955 | AGAAAAGACAGTGTG[A/G]TTTTCTCTAGCTGTG | 11124 |
rs184830096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50563697 | CCTTGTTTACTGAAA[C/T]CAACAAAATGAATAA | 11124 |
rs184830839 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50504476 | CAGAAAAATAAAATA[C/T]GAAAGAGAAGTTAAG | 11124 |
rs184834260 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50892186 | AATCTCCTGGTGTGC[A/C/T]GTTTGCTAAGACCAT | 11124 |
rs184845150 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50646512 | TAAATGCCTAAAACA[C/T]TCTTTGATATAAATG | 11124 |
rs184855025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858582 | AAATTAAAAATGTAA[C/G]CTATCTCATTAATAA | 11124 |
rs184856899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50672583 | CCACGGCGCCTGGCC[A/G]GCAATTTAAGTTTAA | 11124 |
rs184860054 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50604005 | TTAATGAAATAAACA[C/G/T]CAACAGTTACAAGTT | 11124 |
rs184861186 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50708607 | AGTCAGTACCATATA[A/G]TCAGTTTTTAGGCTT | 11124 |
rs184864944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626490 | ATAAAAAGCCCCAAT[C/G]ATGGTACCTCAGAAG | 11124 |
rs184866578 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50686410 | AGCTGGGTGTGGTGG[C/T]GAATGCCTGTAATCC | 11124 |
rs184874817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50665859 | AGTATAGGTACATAT[A/G]TATGCATACCATATG | 11124 |
rs184883901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50704550 | GAGATGGAGCCACGG[A/C]AAAACATTATTTCTA | 11124 |
rs184891473 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749701 | ACTGAGGCAGGAGTA[C/T]TGCTTGAGACCAGGA | 11124 |
rs184911832 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50480464 | GTGTTAAATAGGCTA[A/C]AGCTAACATTCATTA | 11124 |
rs184931334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949595 | GGACATGCAGTCAAC[C/T]ACTCAACTCTGCTAT | 11124 |
rs184932383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515487 | GATTCAGTAGGTCTA[G/T]CTTGGAAGCCAAAGG | 11124 |
rs184935190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50818759 | GGAGGCCAGGCGGGG[A/G]CCGGGAGGCAGAGCT | 11124 |
rs184937220 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50910658 | CTAGCAGTGAGCAAG[G/T]CTCCGTGGCCGTGGG | 11124 |
rs184939517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50931694 | AACACAGTGAAACCC[C/T]ATCTCTACTAAAAAT | 11124 |
rs184950376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50932462 | GTTAAATTTTAAAGC[A/G]CCAAAATGATCTCCT | 11124 |
rs184956694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50916149 | AGACAGACAAAAACA[A/G]ACAAAAGGGGGTCGT | 11124 |
rs184957277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50878621 | ACATTAGCAGCCAAC[A/T]AAGAAGTTATTTATG | 11124 |
rs184958082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50564814 | AATTAATTATCTTAC[A/G]GTTTCATATGTCAAA | 11124 |
rs184960983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50915089 | CTTAAAAACAAGAAC[A/G]GCTGGGCATGGTGGC | 11124 |
rs184967350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50897685 | CTGTGGTATTGAACC[C/T]AATTCTTCAACCTTC | 11124 |
rs184972083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50840008 | AAGGAAGGAATAAGC[C/T]TTTCAAAACTGGTGC | 11124 |
rs184973274 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50726467 | TTTGGGTGGCCGAGG[A/C/T]GGACAGATCACGAGG | 11124 |
rs184973512 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50899344 | CATTTCTAGGTCTCT[C/G]TCTACTGATTTTTCT | 11124 |
rs184977749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50883715 | TGTAAATTAGATACT[A/G]ACAGGAAAAGCTGTA | 11124 |
rs184981476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705756 | CTATAATGAGCTACC[C/T]TTATTTCTTAGCTGT | 11124 |
rs184981835 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50746885 | CAGACGCAGGAAACT[C/G]CTCCCTGCATCCTGG | 11124 |
rs184987967 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50867686 | AAAAAAATTATAGCT[G/T]TTGCTGTGGATGTGG | 11124 |
rs184990733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459286 | GCCCAGAACTCAGTC[G/T]TTTAACTACTACCCA | 11124 |
rs184991603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570774 | AGTAAATTTAGGCTA[C/T]ATAAATCTGATTAAA | 11124 |
rs184995327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50642772 | TAATTATCAATATGG[C/T]TAGATTTAAACCATA | 11124 |
rs184996455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50763574 | ATTTGCCTAGAAGTC[A/G]TTCAGACAACATCCT | 11124 |
rs184998411 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50846566 | CTGATGGAAAAAGGA[C/G]CAATAGTGAGGAACT | 11124 |
rs185002826 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50782717 | AAAATTTATAAAGTA[A/G]AAAAGTTACAGTAAG | 11124 |
rs185006749 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682690 | ATTATCTCAGCCATT[A/T]TGAAAGTAACTTCAG | 11124 |
rs185014368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50807204 | AGAAAGAATCTGATA[A/G]AGCTGAAAGACTCCA | 11124 |
rs185016698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50719034 | AGCTAGCAATGACAG[A/C]TTAGGTTCAAATAGC | 11124 |
rs185017853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50443911 | CAGCAAGAGTGCCCC[A/C]CCTTTCCTGATCAGG | 11124 |
rs185024542 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50824240 | ATTTATTTTAAAAGC[A/T]TCTAGGCTTATCCAT | 11124 |
rs185028024 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467080 | CAGTATGAGGACTGT[C/T]TGTATGAGAGGCTGA | 11124 |
rs185059159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50750568 | CCTAAAGATTACTTT[A/T]GTCTGGGTTCCTTTG | 11124 |
rs185064638 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50788838 | AAAACAATTCTTTTT[A/G]TTTGTTTGTTTGAGA | 11124 |
rs185067944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585980 | ATCACTTGAGCCCAC[A/G]AGGTCAAGGTTGCAG | 11124 |
rs185072945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534333 | TCACCCAGGCTGGAG[C/T]ACAGTGGCATGATCT | 11124 |
rs185075367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50509885 | AAATTAAAAAAAAAA[A/T]GGCCAGGCACAGTGG | 11124 |
rs185078979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937882 | AAGTGAGTGAAAATA[C/T]GAATAAAAACCATGT | 11124 |
rs185081587 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50541477 | AGGGATGTATAGATC[A/G]TGAGATTAGAAAATT | 11124 |
rs185083070 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50902560 | ACTGCCCTAAACTCA[C/T]CTCCCTTTATTCAAA | 11124 |
rs185086949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50827433 | TGCTTGAAGGCAGCA[C/T]GCTCCTTAAGAGTCA | 11124 |
rs185087863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488008 | ATGATATGTTAATTG[C/T]TGTTCCATTTAAAAA | 11124 |
rs185090550 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661175 | CTTTTATTATACTTT[C/T]TAAAAAACACTAATA | 11124 |
rs185094617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50622245 | GATAAAGGGTCCGCC[A/G]TAGCTAGGCTGGTCT | 11124 |
rs185099246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841516 | TTAAAACAAAATACA[C/T]TGAAAAAATAATTAA | 11124 |
rs185103192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50591439 | GCACTTTGGAAGGGC[A/G]TGGCAGGTGGATCAC | 11124 |
rs185106248 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50869550 | AATATTATCTCTCCT[A/G]CATAATCAATTCTGC | 11124 |
rs185109845 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50580620 | CATATAATATTAAAA[A/G]GTAAAAAAAGCTGTT | 11124 |
rs185110119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560612 | TTAGTAGCATGTACA[C/T]TGATGTGCAAAACAT | 11124 |
rs185120463 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50576918 | ACGATCCTCCCACCT[C/T]GGCCCCTCGAAGTGT | 11124 |
rs185122614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598769 | TGAGGTCAAGAATTC[A/G]AGACCAGCCTGACCA | 11124 |
rs185129163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50517869 | ACCATTATCAAAGGC[A/T]TCCAAAAAGTTATTA | 11124 |
rs185129996 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50698473 | CATGGTCATGATCAA[A/T]CCACTTCTGCTAACT | 11124 |
rs185135525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50553420 | CTCATTTGTGGGTGA[C/T]AAAACTTGTGAAGGT | 11124 |
rs185135702 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50495954 | CCGAGACAATAGCCA[C/T]TGAATTTTATTACAA | 11124 |
rs185139313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638922 | AATAAGCACAAACAC[A/C]ATTCTAATACACACA | 11124 |
rs185150103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657513 | GCAGCAATGAGCCAC[A/G]ACTGTGCCACTGAAC | 11124 |
rs185153807 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50618803 | GCCCAGGCTGGAGTG[C/G]AGTGGCACACTCTCA | 11124 |
rs185168247 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50678835 | CTCACGCCTGTAATC[C/G]CAACACTTTGGGAGG | 11124 |
rs185176009 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50602916 | ATGTATTGTTATTAC[A/C]CAAAGTGCTTTACAC | 11124 |
rs185176805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50766865 | GCTCAGCTCATACAG[A/T]TGAGAAAGAACCAGT | 11124 |
rs185178768 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50952706 | TGAGATGTGGGGAGC[A/G]CCTCTGCCCCGCCAC | 11124 |
rs185183671 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50625196 | TGAGCCACCGCTCCC[A/G]GCAGAGAATCCTACA | 11124 |
rs185186939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50920329 | AAAAGTAAAGAAAGA[A/G]AATATGCTTTGGAAG | 11124 |
rs185187338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50584236 | CTATAGTACACATCT[C/T]GTAAGTGGAAGTGAA | 11124 |
rs185189390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810335 | AAAAACAAAACAACA[C/T]GATCATCTCAAGATA | 11124 |
rs185196665 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50552023 | CTGCAGGCCAGGTGC[A/G]GTGGCTCATGCTCAT | 11124 |
rs185197269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50663949 | TTACTACAGACTTCA[C/T]TGCATTCTCAGTTTA | 11124 |
rs185203612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912167 | ATTATGGAGAGAGAA[C/G]GGCTTGAGCTGCCGC | 11124 |
rs185206459 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50860010 | ATAGGGAAAGGACTG[A/C]CTATTGAATAAACAA | 11124 |
rs185206860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460433 | TCTAGTGTTCCTAAG[C/T]AAAGGAGGGCTGTGA | 11124 |
rs185208024 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684869 | TTCTGTATAGAGAAT[A/G]TAAACATCAGTAAGA | 11124 |
rs185208070 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50895150 | CCAGACTAAATAAAA[A/G]AGGAAAATAAATAAA | 11124 |
rs185213994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50921996 | ACATGGTGAAACCCC[A/G]TCTCCACTAAAAACA | 11124 |
rs185214377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50644991 | CACTCTTGTTCAGAA[C/T]AGAATTCATTTCACA | 11124 |
rs185215173 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50885619 | ACAGACCATTTGGGT[A/C]TTGTTTTTGTATCCA | 11124 |
rs185216650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50710077 | GACCTCCATTATGGA[C/G]GGCTTCAAATGCTAG | 11124 |
rs185216853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939078 | CCATGTGAATTTTAG[A/G]ATAGTTTTTTTAGTT | 11124 |
rs185219827 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503872 | TCAGTGGATATGTGG[C/G]ACTTGGCTTGACAGA | 11124 |
rs185221021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751071 | GATGGATTATAAGCT[A/G]TTAAACAAGCTGTAC | 11124 |
rs185222714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50700901 | GCTGCATTATAAATA[C/T]TAAATTTATTACTTC | 11124 |
rs185222908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50880973 | TGCTATATAAAAGAA[C/T]TACCTGGATATATAT | 11124 |
rs185224883 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50729721 | CTATCTCACAGAACT[A/G]TTTATGTAAGATTGG | 11124 |
rs185231779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862861 | TGCTAAATATACATA[C/T]ACTAAACACTGGAGC | 11124 |
rs185232278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50767767 | GGAATTTGTCACCAC[A/G]AGACCTGCCTTATAG | 11124 |
rs185238256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50843056 | TTTTGGAATTATTTA[C/T]TAGCTTTATAAAATA | 11124 |
rs185238825 | snp | A/G | 0.00162766 | 0.0284813 | intron-variant | FAF1 | GRCh38.p7 | 1:50596077 | TGCGCAGGTAGGTGG[A/G]GGATGGGCCTTCTGT | 11124 |
rs185252341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50628612 | TCTTGGATGTCAAAA[C/G]CTTAAAAGTGATTAA | 11124 |
rs185284439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50807660 | AATCAACCAAAGAGA[A/G]GAAAGAATCTCAGAG | 11124 |
rs185290908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824633 | TACATCCAAAGAAGA[C/G]ATAGTTGCACTCCTA | 11124 |
rs185291788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50482052 | ATCCTTTTAAATGTA[C/T]AGTTCTGTGAGTTTT | 11124 |
rs185294259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50668401 | GGTCAGGTTATCTGA[A/G]TCTAACTTGCTACTT | 11124 |
rs185301457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705340 | TCTTAGGCATACTGC[C/G]CAAGGGCAGGATGGA | 11124 |
rs185305860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770751 | CAATTAGAAAAGACT[A/T]TTTTAAAATTCATAT | 11124 |
rs185307807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50950108 | TCTTCTCAAAGTGCT[A/G]GGAATACAGGTGGGA | 11124 |
rs185309683 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50746155 | ATAACTGGAGGAAGA[A/C]ATTTCTAAGGAACAA | 11124 |
rs185323550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456435 | CCAAGACCACCGTAA[A/G]GAGGAGGTAAGGGGA | 11124 |
rs185323809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50915511 | AAGATAAAACCTAAC[C/T]GTTTACAGAGATGAT | 11124 |
rs185324136 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50812960 | ATTATCCCAAACTAA[C/T]GCAGGTACAGAAAAC | 11124 |
rs185326511 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50527273 | TTCATGTGCTATTGG[C/T]CACTTGTATATCGTC | 11124 |
rs185335988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50446314 | CACTTTTTAGTACCT[A/G]AGCATAAACTACAGG | 11124 |
rs185341777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50477244 | GCACTGAATAACCAC[C/T]TACCTTATAGGGGAT | 11124 |
rs185344240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50883181 | CTGGGCAACTAACAG[A/G]TGTATGGGACAATCT | 11124 |
rs185357484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50576003 | AAGAGCACTGTTAAA[C/T]GTGAACTACTAATTT | 11124 |
rs185367675 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50549412 | CTCCTGGGCTCAAGC[A/C/G]ATCCTTCTGCCTCAG | 11124 |
rs185373586 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50522680 | ATCAATAACTTTTCC[A/T]ATTTCCAGCCCATAG | 11124 |
rs185383939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50499706 | ATATAAAATAAATAA[C/T]AAGCAACCCCTTCCC | 11124 |
rs185390488 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50847888 | ACAAATGCACACATA[C/T]ACACACACACACACA | 11124 |
rs185394232 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468449 | AGGTGCACGCCACTA[C/T]ACTTGGCTAATTTTT | 11124 |
rs185401480 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50647489 | CTGCCAATTTGCGAA[A/T]CATTTTTTTTTCTTG | 11124 |
rs185401646 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687458 | AACACATGAAATGAT[A/G]CTCAAAACTGGCCGG | 11124 |
rs185434570 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50794286 | AAAAAATTTGGACTG[A/G]GAAGAGAAAAAATGA | 11124 |
rs185446459 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50932137 | ATGGGGACACAGCCA[A/G]CCATATCATTCCACC | 11124 |
rs185447981 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493253 | AGCCAGGCTGGTCTC[C/G]AACTCCTGACCTCAA | 11124 |
rs185448377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50448617 | TACAAGGTACGAGGG[C/T]CTGCAGTGTCCAGCT | 11124 |
rs185449524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50762995 | GCGCGTTGGCTCATA[C/T]CTGTAATCCCAGCAC | 11124 |
rs185455619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50830242 | GCTGCCTCAGCCTCC[A/G]GTGTAGCTGGGACTA | 11124 |
rs185459798 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50898339 | CAACAACAACAACAA[A/C]AAAAAACTCTAGGAG | 11124 |
rs185475899 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50867408 | CTGACAACCCACAGA[A/G]TGGGAGAAAATCTTG | 11124 |
rs185478252 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50541003 | TCTAGCTGATGAGCA[A/G]AGTCCTGTCATCACA | 11124 |
rs185496852 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50576346 | GAGTCCCTTAATTTA[C/T]GTATAATATTTGGAA | 11124 |
rs185511558 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50656841 | TGAGCTGAGATCGTG[C/T]CACTGCGCTCCAGCC | 11124 |
rs185522439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618642 | CATATATTTAGGATA[A/G]TTAAGTCTTCCTGTT | 11124 |
rs185532302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695039 | AGGCTAAGAAAGTCA[A/T]TGTGTAAAACAAAAT | 11124 |
rs185538304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760057 | CTGGATACTCGCCCT[C/T]TGTCAGATGAGTAGG | 11124 |
rs185538320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50811015 | GTGCCACTGTTCCAG[A/C]CTGGGTGACAGAGTG | 11124 |
rs185542382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723442 | GAACTATTTGAAAGC[A/G]TCCTCAGCATGTCCT | 11124 |
rs185542476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778760 | AGGAGTTCAAGGCCA[A/C]AGTAAACTAAGAGTG | 11124 |
rs185546043 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50959166 | TATTAAGCTTGTGAA[C/T]TCATTGCAGAGATAC | 11124 |
rs185546712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50828017 | TGACTGTAAATATAT[G/T]TGAAGATACAAAGAC | 11124 |
rs185550711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50803676 | AATGCCTCACCTGAG[A/G]CTGAAGAATGAGTGA | 11124 |
rs185569167 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50514892 | TACACATCTGCCTGG[G/T]AACCTAGGATGGAGC | 11124 |
rs185579075 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50924296 | TGAAAAAAAAAAAAC[A/C]AGAAACCAATCCCAT | 11124 |
rs185587215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470734 | ATTTCTCTTTCAAAG[A/G]TGCAGAAATAAAAGT | 11124 |
rs185612463 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50597249 | GAAAACATGACTTTA[C/G]CAGAAACACCTTCCT | 11124 |
rs185618441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866115 | ACATGATAATCTCAA[C/T]AGATGCAGGAAAAGC | 11124 |
rs185640414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523870 | ACATGCAAGTGTCTT[C/T]ATAACAGAACAATTT | 11124 |
rs185661306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50638505 | GCTGGAGTGCAGTGG[C/T]GCAATCTCCGCTCAC | 11124 |
rs185666636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50592556 | TTCTCCCAGCTAAAG[A/G]AAATATAACTACAAT | 11124 |
rs185668382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50954573 | TTTGAGAGAGTCTTA[C/T]GCTGTCACCCAGGCT | 11124 |
rs185671527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50678006 | TTGTGAGATATGTAG[A/G]CTAGAGGCAAAACAG | 11124 |
rs185672378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50573165 | GGCTGATGGCACCAT[C/T]TCAGCTCACTGCAAA | 11124 |
rs185674548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550006 | CTTTGACATTTACAC[A/G]TAATGTCCTCATGTA | 11124 |
rs185676813 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50715199 | TTATTTGCAACAAAA[G/T]AAAATGAAAGTTAAC | 11124 |
rs185679532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50561899 | AGGAAGGAAGGAAGT[A/T]GTGTAAACCAATGGG | 11124 |
rs185683524 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50537350 | GGTACTACATATTTA[A/C]GCCCTTATTGATCAA | 11124 |
rs185687356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653487 | CCCCAAGTAGCTGGG[A/G]TTAAAGTCACAAGCC | 11124 |
rs185687626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50944156 | GTTTTGCATGGAAGG[C/T]ACATGACCTGGAGCC | 11124 |
rs185691425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614638 | TAAGGTCAGGAGTTC[A/G]AGACCAGTCTGACCA | 11124 |
rs185697629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50905184 | GAATGATGGTTTCCA[C/G]CTTCATCCGTGTCCC | 11124 |
rs185698339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948718 | TTTAGTAGAGATGGG[A/G]TTTCACCATGTTGGC | 11124 |
rs185700977 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50635194 | ACCATGATGAAAATT[C/T]GAAATTCACTTATGT | 11124 |
rs185708930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50929343 | ACATTGAGTACTAGT[A/G]TATAAATTTTATCCT | 11124 |
rs185711493 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50887420 | CTTTGGTTGCCATTG[C/T]TTTTGGTGTTTTAGA | 11124 |
rs185712682 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50583035 | TTTCCCACTTCAGTT[A/C]ATTTATTCCAGAATT | 11124 |
rs185716614 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50602386 | TGTATTTGTATGTCA[A/C]GATGTATCCAACTGT | 11124 |
rs185716902 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50906879 | CCTTTCTTTATTTCT[C/G]CTGCCTGGTTGCCCT | 11124 |
rs185721464 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50871958 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11124 |
rs185726265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849534 | CCCAAAATTCAAGCA[C/T]AGAATTTGTGAGAGT | 11124 |
rs185738816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50601379 | CTTCTTTCTTTAAAA[A/G]TATGAATTAGTAGGC | 11124 |
rs185749996 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50882806 | GCGTGGCCAACATGG[C/T]GAAACCCCATCTCTA | 11124 |
rs185762017 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50845605 | CCACCTGCACAGAAG[A/T]TGCTAACTGCTTGTC | 11124 |
rs185789228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607698 | TCTGAAAGCCTTCTA[C/T]ATGACCTCCCCAATT | 11124 |
rs185795227 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50944898 | ATATAACCTCCCACC[C/T]CTTCCATTCTGATCA | 11124 |
rs185801176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50567414 | AAAAATTTTACTTTC[C/T]TACACTTTAAAAAGG | 11124 |
rs185805648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648802 | GTGGTGGCGCATGCC[G/T]GTAATCCCAGCTACT | 11124 |
rs185821024 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | FAF1 | GRCh38.p7 | 1:50907952 | TTATCTAGTTCTTTT[A/C]ATTGTGATGTTAGGG | 11124 |
rs185821147 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50716025 | TATGTCTCATTCAGA[C/G]AGTACTTCTGCAACC | 11124 |
rs185837313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875817 | TCATGAACTTACCCC[A/C]CTAACTGAAATTTTG | 11124 |
rs185837659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50688600 | GGTGGATCACCTGAG[A/G]GCGGAAGTTCGAGAC | 11124 |
rs185855983 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50838725 | TCTCTCAGAGAAATA[A/G]CATGCAGAGGATTTT | 11124 |
rs185856463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452007 | TTTGGTCACTATACT[A/G]TTAAATGACAATATA | 11124 |
rs185864720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50473198 | GTTTCCTTTCAACAG[C/T]AACTTTCCACAGTCC | 11124 |
rs185871629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50547858 | TTTTTTGAGGAACAA[C/T]AATCATAAATAATAA | 11124 |
rs185873163 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50528326 | CTTTTAGCAATAGAT[A/T]TTTTACTTTAGTGAT | 11124 |
rs185875058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50471726 | CAGTGGACTCTTAGA[A/G]TTCATCTGCCATTCC | 11124 |
rs185884934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50441683 | ACCTGCAAGGCAGGT[C/G]TTGTTATTCTCATTT | 11124 |
rs185887812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543830 | AATACATTATAGATG[C/G]TGCATTTGTACAATA | 11124 |
rs185891307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464970 | CTTTACATCCAATCA[C/T]CTCTCCAATCTTCCC | 11124 |
rs185899168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50495215 | GTTATTCACTCTTTC[C/T]ATATTTTTTGTACCT | 11124 |
rs185917044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565466 | TTTTAAAAAAGTGTC[A/C]TAAGGAGTTAATAGG | 11124 |
rs185922674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50834450 | AGAAAATCAGAGTCA[C/T]TGGGAAAGACAGGTA | 11124 |
rs185929869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588027 | CATGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 11124 |
rs185933597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50542306 | TGTCAATTCATTCCA[C/T]TATAATTAACAAGAA | 11124 |
rs185934396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925345 | AAAAGGCTTCTCCAC[A/G]GTAAAAGAAACAATC | 11124 |
rs185937730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516145 | CTGCTAGGTGGAAGA[A/G]CTAGGATTTGAATTC | 11124 |
rs185950290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50670065 | GGTGGAGGTTGCGGT[A/G]AGCCGAGATTGCGCC | 11124 |
rs185950648 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50629093 | TTTTAAGTGATATCT[A/T]TTATTGTTATTCCCA | 11124 |
rs185954472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50587016 | AGTCTTTGCTTAATC[C/T]TGCCTAGTACTCACC | 11124 |
rs185955017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695494 | AATGAATACAAATTA[A/T]TCCTCTGGAAATGTG | 11124 |
rs185955098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50950208 | TTCTCAAAGAACCAC[A/G]GCTAAGAAAACCTAA | 11124 |
rs185964568 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50890980 | GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTACA | 11124 |
rs185973934 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50675359 | TCAAGAGCCGCCCAG[A/T]AAGTAACACAAATGA | 11124 |
rs185975087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855699 | CATGAAAACAGGATA[A/G]ATGATAAAATGTAAA | 11124 |
rs185984425 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50653986 | AATAAAGGTTTTGCT[A/G]TTTTCTGATTATTAA | 11124 |
rs185990541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871247 | CATAACATGAAAATG[C/T]AAGGTGAAGCAGCAA | 11124 |
rs185992193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50692454 | TCCTCATTCCTACCC[A/G]TCCACACCCCACCAC | 11124 |
rs185999820 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50732825 | CAGTTTCAAATTGCT[A/G]TTTGCTGATGTATTG | 11124 |
rs185999830 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50849245 | GCACTATAGCCTAGG[C/T]GACAGAGTGAGACTC | 11124 |
rs186004499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50711351 | ACAGTGCTTTTGTAG[C/T]AGTTACTTTTCATGT | 11124 |
rs186012811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777985 | AAGAATGTTTATGTA[A/T]GCCAAAAACATGTAC | 11124 |
rs186014928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50801183 | TTGCATTATTAAGAA[A/C]TGCCTCAAATTGTTG | 11124 |
rs186020959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751779 | CCTCCATAGTTATAA[G/T]AAATATTTTCCTGTA | 11124 |
rs186026587 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50819693 | TGTATATATATATAC[A/G]TATATATATACATAT | 11124 |
rs186031649 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562500 | AAAATCTGCCACCCA[A/G]AAGACTAGGAATGCT | 11124 |
rs186032825 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447329 | ACGGGGTTTCACCGT[G/T]TTAGCCAGGATGGTC | 11124 |
rs186033586 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50591784 | ATCTTCCTTTTCCCC[C/T]GACTTTCTTCTGCAC | 11124 |
rs186049999 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50512398 | TAAGTCTTTAATCCA[C/T]CTTGAGTTAATTTTT | 11124 |
rs186066745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50673485 | CTAAAAGAGACAAAG[C/T]TTCTGTGTTCATGGA | 11124 |
rs186075466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50634734 | ACTGATTTTTCAGTG[C/G]CATGCTTAATATAAT | 11124 |
rs186077594 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50948596 | GGAGTGCAGTGACGC[A/G]ATTTCAGCTCACTGC | 11124 |
rs186116857 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50886534 | CCCTCCCCACTCCCC[C/G]CACCCCACAACAGGC | 11124 |
rs186135799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742398 | GAGGGGGGGTGTGGC[A/G]GGGGAGAGAGACTCT | 11124 |
rs186138185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848747 | AAACATCAGACAAAC[C/T]CAAACTGAGGAACAT | 11124 |
rs186144033 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50778312 | ACGTGCAATAAATAT[G/T]CTCTATCTGGATCTG | 11124 |
rs186154214 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50783591 | TTAACATAAAAAAAT[C/T]GGCCAGGCGCGGTGG | 11124 |
rs186168218 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50613770 | ATATACACATGCATT[C/G]CAAGAAAAATCTTTT | 11124 |
rs186168289 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50539195 | GTGAAAAATTCAATC[A/T]TCAATATACAGTGAC | 11124 |
rs186184941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50571651 | TGTGTCTCTGAGTTC[A/G]GTGCCTCACTAATCT | 11124 |
rs186189631 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50653220 | ACATCCCTATCCTTA[G/T]CCATAGATGACCAGC | 11124 |
rs186197486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50639431 | TTTATCATGAATGTA[C/T]GCTAAATTTTATTAA | 11124 |
rs186206170 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961244 | GGGGTTTCACTATGT[C/T]GGGCAAGCTGATCTC | 11124 |
rs186210868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606798 | GAGCCACCGCGCCTG[A/G]CTGAGCTGTGAGGGT | 11124 |
rs186215597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691537 | ATGAACCACTGCATA[C/T]AGCCTACCTTTTAAA | 11124 |
rs186215938 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50928652 | GCCGAGCATGATGGC[A/G]GGCGCCTGTAATCCC | 11124 |
rs186216731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50679273 | TCAGCTGCTCTGCCT[A/C]TGGAGTAACCATTCT | 11124 |
rs186217121 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50578655 | TCTAAAATGGGAATA[G/T]GAGGATTATATATCC | 11124 |
rs186220735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50925017 | AAACAGATACATAGA[C/T]CAACAGAACAGAGAA | 11124 |
rs186227579 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50944579 | GCAAGAGGGTCAAGG[C/G]AATTTGCATAAAACC | 11124 |
rs186230652 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50587833 | CTAAATCATAGGGGG[G/T]AGGAATCAGGAAAAA | 11124 |
rs186231343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50658922 | CGTAGATGTTACCAG[C/T]ATATGGATGAAGCAC | 11124 |
rs186233652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50696055 | ACTTGAAAACAATTC[A/G]AATTATATAAGTCAA | 11124 |
rs186237697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50907384 | TGGTATCAGGATGAC[A/G]CTGGCCTCATAAAAT | 11124 |
rs186238569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50950390 | TTTCATGGGGGGAGC[A/G]GAGAAATAACTTTAC | 11124 |
rs186243755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890038 | GACTTGCTTTGTGAA[C/T]CTGGGTGCTCCTGTA | 11124 |
rs186244199 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50904648 | GTTTGCAAATATTTC[C/G]CTAGTGGATTTTATT | 11124 |
rs186246965 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50628947 | TATTATTTATGTGGT[A/C]ATATCAATATAATTC | 11124 |
rs186251219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669630 | ACATATGAAACTGCA[C/T]TATCAAATTACAAAC | 11124 |
rs186251979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50716800 | CCAACCAGCAGGATG[C/T]GGGCAGAGACAAATA | 11124 |
rs186252462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648032 | GGGAGGCCGAGGCAG[A/G]TGGATAACCTGAGGT | 11124 |
rs186254209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875283 | TATTTTAATTAACAA[A/G]AATTGAATATATTTA | 11124 |
rs186254481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933904 | CCCATCAGATCTTGT[A/G]AGACTTATTCACTAT | 11124 |
rs186256718 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705619 | TTCTAGGTCAAGTCA[A/C/T]TTAGTATATCTACAG | 11124 |
rs186258896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721943 | CTCCTTTTCTGCTGC[A/G]CTGCTAAAACCTCAC | 11124 |
rs186261301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50755430 | GGCCTTGGGCAGCTC[C/T]GCCCTTGTGGCTTTG | 11124 |
rs186264015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50870505 | ATGGCATCCCTGCAT[C/T]GAGCAAGTCCATCAG | 11124 |
rs186265102 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50916569 | TGAACCTCTCTAAAC[C/G]TAGAAACAAAGATCT | 11124 |
rs186265514 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50687618 | AGCCAGGCATGGGGC[A/G]CGTGCCTGTAATCCC | 11124 |
rs186265632 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50772593 | TCTAAACGAACTAAC[A/T]CAGGAACAGAAAACC | 11124 |
rs186268313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50489370 | CCTTCAGGCCTTTCC[A/G]TTGCTTGTTAGATGG | 11124 |
rs186270243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726188 | TTGAACTCAGGAGGC[A/G]GAGGTTGCAGAGAGC | 11124 |
rs186271290 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50758887 | TTGCTCTGTTGCCCA[A/G]GCTAGAGTGCAGTGG | 11124 |
rs186289178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582052 | TTTTTTTGGGGGGGT[G/T]GGCAGGGGCCCAAAG | 11124 |
rs186293481 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50500317 | TGTTGTAAAGACAGA[A/G]AAAAAATGGAAAAAA | 11124 |
rs186301805 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50833410 | AGGTGTGTGGGGGCG[G/T]GTGTGTGGGAGACAG | 11124 |
rs186302530 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50536493 | GGCATTTTTCCAGAG[A/G]GCTTGACTAACATGA | 11124 |
rs186309140 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50623503 | GAACCCGGCAGGTGG[A/C]GGGCAAGTTGCAGTG | 11124 |
rs186359022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50928502 | AAAACTGAGGAAGGC[A/G]GCCAGGCGCAGTGGC | 11124 |
rs186369498 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50894873 | GGGGTTACAGCAAAA[G/T]CAAGAGGGAAGTACC | 11124 |
rs186369749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50691751 | ATGCACCACCACGCC[C/T]GGCTAATTTTGTATT | 11124 |
rs186380423 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50730648 | CATGCCAGAAGCAGG[A/G]CTCCGCTACTCTTGA | 11124 |
rs186381893 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50862119 | GAAAAAAAAAAACAC[A/C]TGGGAATGAGGACCA | 11124 |
rs186389630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768104 | AGGGACAGAGAAAAA[C/T]CTACCAAGTCAACAG | 11124 |
rs186418075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50511409 | TAACCCCCCACCCAA[C/T]CCAACAGGCCCCGGT | 11124 |
rs186420767 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468981 | TAAAGAAATATAAAC[C/T]GCCCTTGCTAGTATT | 11124 |
rs186436516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512021 | CTTTTTTTCATGTTT[C/G]TTGGCCACATAAAAG | 11124 |
rs186442734 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490435 | GAAGGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA | 11124 |
rs186454354 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50446894 | CTCTGTAGATTAGGA[A/C/G]ACAAGACCCAGAGAC | 11124 |
rs186455290 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561716 | CTGTAGTTCCAGCTA[C/T]TCGGGAGGCTGAGGC | 11124 |
rs186461338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50889717 | TAGTTTGATTGCACT[A/G]TGGTCTGAGAGACAG | 11124 |
rs186462002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50477902 | AAGTGCTTAGTATGA[C/T]TGTAGGCACGTACTA | 11124 |
rs186469174 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874930 | ATGGACCACCATGCC[A/C]AGCTAATCTTTGTTT | 11124 |
rs186477069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50853073 | TGCTTGGCTGCTTTC[A/G]GATGAGGACAGAGAC | 11124 |
rs186478577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50755548 | GATCTACCATTCTGG[G/T]GTCTGGAGAACAGTG | 11124 |
rs186480600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50558830 | GCTTTGATTCAAATA[C/T]GATGCATGTGCAACC | 11124 |
rs186482818 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50773927 | TGAAACATCATATTG[A/T]ACCTCATAAACATAC | 11124 |
rs186484104 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50643674 | CTCAGCTCACAGCAA[C/G]CTCCGCCTCCCAGAT | 11124 |
rs186486350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50837490 | TTTTTGGCAAGAATA[C/T]TACATAAGGGATTTC | 11124 |
rs186494550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50797312 | TGTGAAAACCACCAT[C/T]TTATAATCTGACCTT | 11124 |
rs186495117 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602006 | TCCTTTTGTAAAATA[C/T]AGGTACGACCAACTA | 11124 |
rs186497765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50815955 | TCGCTTGAACCTGGG[A/G]GGTAGAGGTTGCAGT | 11124 |
rs186505841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834074 | CGGGCGGATTTCCCC[C/T]TTGCTGTTCTCATGA | 11124 |
rs186526933 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | FAF1 | GRCh38.p7 | 1:50441355 | TTGAGTGAGACGAGC[A/G]TGTGGGTGGGTTGGC | 11124 |
rs186533871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50485580 | GGCAGGGGAATCACT[G/T]GAACCCAGGAGGCAG | 11124 |
rs186538091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948168 | AGAAATAGAAACTTT[C/T]CAAAGGAACATGAAA | 11124 |
rs186540137 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50621884 | AAAGATTCCCCTGCT[A/G]GCCAGGCACAGTGGC | 11124 |
rs186544965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579294 | AAAATGTGTGAGGTA[C/T]ACATAGTATATCTTA | 11124 |
rs186546410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545696 | AGTCACTACTATACA[C/T]TGTTAGTATAAGTGA | 11124 |
rs186549356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50599725 | AGAAAAAGCATGTGT[A/G]TTTCAGTTATATGCT | 11124 |
rs186552997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660213 | TTCTTAGGAAAGTAA[A/T]TCTTAGGAAAAGTTG | 11124 |
rs186565036 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674643 | ATTTTATTTTTTGGC[A/G]TGTTTTACTGCATTA | 11124 |
rs186567030 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50641047 | CAATGTTGGCCAGGA[C/T]GGTCTCGATCTCTTG | 11124 |
rs186572367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50911900 | AAATCAATCAGGCAT[A/G]GTGGCATGCCCCTGT | 11124 |
rs186573701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50710856 | ATCCGCCCATCTCAG[C/T]CTCCCAAAGTGCTGG | 11124 |
rs186578347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50697611 | CTCATGGAAAAGTCA[G/T]TGTCAAAATTAAACA | 11124 |
rs186592985 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50939190 | TATTCATTCTTCCAA[C/T]GCATAAGCATGAAAT | 11124 |
rs186593511 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880534 | AATACTAGAGAACTC[A/G/T]TACACTATCTCCACA | 11124 |
rs186600283 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50644313 | CTGAGGTGTCTCTAC[A/C]ATGTGTAGTTGGAAG | 11124 |
rs186604455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684325 | GTCTATGACAATGGA[A/C]CATTTTAAAACTCAG | 11124 |
rs186606430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50751255 | TAGTTGATAATGAAA[C/T]ACTAAATACTAAGTA | 11124 |
rs186607636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50842439 | TTAAGCATATATTTT[A/G]ATACTACATGCATTA | 11124 |
rs186618727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50790391 | ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 11124 |
rs186619644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904920 | ACTTTAAGTTCTAGG[G/T]TACTTGTGCACAATG | 11124 |
rs186625630 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50936358 | AAAAAGAAGAAGAAT[A/G]AGAAATACAGAGGAG | 11124 |
rs186630166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50721152 | AACAAAAAGTTGTTT[C/T]GTAAAGCACTTTGGG | 11124 |
rs186642025 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | FAF1 | GRCh38.p7 | 1:50918048 | TCTGGCCTCAAGTGA[A/T]CTGCCCACCTCAGCC | 11124 |
rs186654037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820540 | TCTCTTAGCAAATTT[C/T]GAGACGTAAACAATA | 11124 |
rs186655112 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50901212 | GGATTCCACCTGCAG[A/G]GCTAAGATTTATTGT | 11124 |
rs186655258 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50885211 | ATCTTTTCAAAAAAA[A/C]CAACTTTGCCTTTCA | 11124 |
rs186662668 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50868903 | CATTTAACTCTATAA[A/G]TGTCAATTAAGTCTA | 11124 |
rs186684737 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50790836 | TACTATTGCTTTGAA[C/T]AGTGTTCATCAAACT | 11124 |
rs186698619 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50458826 | AGCTCTATGAATTTC[A/G/T]TACTATCATTATCCT | 11124 |
rs186707140 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828561 | GGCCTGAGCCACCGC[A/G]CCCGGCCAAGAAGGG | 11124 |
rs186722120 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50502426 | TTATTAGCAAAAATT[A/T]TGATGGTCACATACA | 11124 |
rs186732402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479528 | TGTTATCATTTTTGT[C/T]ATGATTATTCCTTTT | 11124 |
rs186735127 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50749496 | TCCTCATATTTTAAA[A/T]ATTACTCTCTATTGC | 11124 |
rs186741069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50728396 | AGCCAGAGGGACAGC[A/G]ATAAAAGACGAAGTT | 11124 |
rs186746912 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50765952 | AAAAAATTAGCTGGG[A/C]GTGGTAGCGGGTGCC | 11124 |
rs186754291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505570 | AAATGCTTACTTTCA[A/T]TCACAGGTTAGTAAA | 11124 |
rs186755846 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50550651 | ACCACATCACCTAAA[C/G]TCCCTAAAGAATTAT | 11124 |
rs186757955 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50525179 | GCGTGAGCCACTGTG[A/C]CTGGCCCCCATATGT | 11124 |
rs186758491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463683 | TGCACAAGGTCTGGC[A/G]TGGAACAGAACATTA | 11124 |
rs186762368 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50786597 | TTACCAAAATTTTTT[A/T]AAATAAAAAACAATC | 11124 |
rs186768573 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50808786 | TATTTTATTGTTTAC[C/T]CAAAGTCAATCAGGA | 11124 |
rs186779756 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50827064 | TCTGCCCAGCCACCC[C/T]GTCTGGGAGGTGAGG | 11124 |
rs186795275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624603 | AAAGGATTTTAAAAC[C/T]GAAAAACAGAGGGCT | 11124 |
rs186808673 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50506366 | CAAACAAGCCCTCTC[A/G]CAATTCTCACAGACT | 11124 |
rs186834220 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50756464 | ACAAGTCTCCAGGAG[A/G]TTCCAAACTTTCCTG | 11124 |
rs186835490 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50738367 | GGAATCACTTGAATC[C/T]GGGAGGCAGAGGTTG | 11124 |
rs186836013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50953857 | GTGTTACAGAAAACA[C/T]AACTGAAAATAACAT | 11124 |
rs186844421 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50663479 | ACAATCTCAGCTCAC[C/T]GCAACCTCCGCCTCC | 11124 |
rs186845024 | snp | A/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50775063 | TAATCTGATTGAGCA[A/G/T]CTCTTTGCATTGTAT | 11124 |
rs186852763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50799183 | ACAGAGTAATAGAGA[A/G]GATAGAGCATGGCTT | 11124 |
rs186853753 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50886997 | TACAGTCCCACCAAC[A/C]GTGTAAAAGTGTTCC | 11124 |
rs186855561 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50700150 | TCCCTTTCATACCCC[C/T]CTTTTTTTTTTTATT | 11124 |
rs186857468 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50741349 | GTGGCTGGAACATGG[A/T]AAGTGAGAGTAAGAA | 11124 |
rs186858715 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554707 | TATCAAACCTCACCA[A/G]AATTTATTTTAAAAA | 11124 |
rs186869284 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50930768 | AGATCGTGCCACTGC[A/G]CTCCAGCCTGGGAGA | 11124 |
rs186877966 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50914910 | ACTAAGCATGTTTCT[C/G]TCTATCCTTGGATTT | 11124 |
rs186879989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951677 | CTAAAACAACATGAT[C/T]TGTCTCTTTAATAAA | 11124 |
rs186887523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50955653 | ATATATGCAAAAGAA[C/T]TGAAAGCAGAAGCTG | 11124 |
rs186889345 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50768418 | TAAAATCTGAACTCA[A/G]TATTAGACCAAAAGA | 11124 |
rs186891446 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50896980 | AAAAAACACAAAGAA[A/G]AGAAAAAGTCAATTG | 11124 |
rs186892715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50917469 | TCAGAGGGCCTCAAA[C/T]ATAATGCCAGATTTT | 11124 |
rs186892795 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50598965 | ACAAGAGTGAAACTC[C/G]GTCTCAAAAAAAAAA | 11124 |
rs186900322 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940793 | GTAACTACGTAATCT[C/T]AGTAGCAACCATTGT | 11124 |
rs186900494 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50882654 | AATAAATAAATGTGT[A/G]TGTATGTATGTATGT | 11124 |
rs186908962 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | FAF1 | GRCh38.p7 | 1:50864795 | GCAAGGACTTCATGT[C/G]TAAAACACCAAAAGC | 11124 |
rs186911139 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50811150 | GACCAGTGTGAGCAA[C/G]ATGGCATAACCCCGT | 11124 |
rs186918132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844740 | GTATTTTCCAAGTCA[C/T]GTTATGGGTATGAGA | 11124 |
rs186921256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884703 | AGTATTAGTTGGGGA[C/T]ACTGAACTGTAGTTT | 11124 |
rs186942716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50957763 | GGTTAACAGTTAAGC[A/G]TAATAATTGTCACAC | 11124 |
rs186944076 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50706686 | AAACTAATATTAAAT[G/T]AGTATTAAACTAATA | 11124 |
rs186945865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50646608 | AACATAATCAAATGT[C/T]CCTTTCACTGAGAAG | 11124 |
rs186951260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50854641 | ATAGAGTTTGGAATA[A/C]CTCTTTTGCAGACAG | 11124 |
rs186955802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626540 | CTAGTGAACAGAGAA[C/T]AAGAGGCAATAAAAT | 11124 |
rs186959447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50747822 | TCTGGTGCTGTTCTT[A/G]TGATACAGTTCTCGT | 11124 |
rs186961791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943594 | GTCAGGAATGAATTT[C/T]GCACTGCCTAGTCTA | 11124 |
rs186967718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50666528 | GACACTTTTATAATT[C/G]TAACGTGTATGAATC | 11124 |
rs186969139 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50450572 | TATGTCCCTAATGGG[C/T]TTTGGTGTTCCAAAC | 11124 |
rs186969324 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50923360 | TTGAGGCTGCAGTAA[G/T]CTATGATCATACCAC | 11124 |
rs186971467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906553 | ATCCTCTTTTAGTTC[A/C]TTGAGCAGTGGTTTG | 11124 |
rs186971935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50704651 | GGTTGAAAATGAAAT[C/T]ACAATTTATACATAT | 11124 |
rs186976729 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50752603 | CTCTACTACTTATCC[A/G]TTTTCCACTTACTGT | 11124 |
rs186978558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50733016 | AGTTCCCAATAACCA[C/T]TATCTCTGTGTCGTC | 11124 |
rs186981310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815495 | TTGATTCCATGTCTT[C/T]GCTATGGTGAATACT | 11124 |
rs186981482 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50686461 | GCAGGAGAATCACTT[G/T]AACCTGGGAGGTGGA | 11124 |
rs186990572 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819753 | TACATATATATATAC[A/G]TATATATATACGTAT | 11124 |
rs187005763 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50551566 | ATGGTTTATGAACAA[C/T]TAGAATACAGTAGCG | 11124 |
rs187018089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616415 | AACACAGAATCTGTA[G/T]GTTGCCTTTGTCACT | 11124 |
rs187033108 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575751 | CAGACAAGATAAGCA[A/G]ACTGGGCATATTTTC | 11124 |
rs187033814 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | FAF1 | GRCh38.p7 | 1:50485952 | GCAAGGGGAAATGGC[A/G]CTCCCATGATCCAAT | 11124 |
rs187036184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50595752 | TTTACTATGTTGGCC[A/G]GGCTGGTCTCGAACT | 11124 |
rs187039321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50702325 | TAAACTGTTGACAAA[C/T]CTGAATTCTCAGCGT | 11124 |
rs187040182 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50827308 | CTTCTGCCTTGGGAG[A/G]CTGTTAATCTATAAC | 11124 |
rs187040627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50577644 | TATGGATTGTTTATA[C/T]TGTTTTATTTACCTC | 11124 |
rs187042736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685526 | GACCTTACTGTGAAC[C/T]CTTAAATACTACTTA | 11124 |
rs187046971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50637948 | AACACATGATCATGG[C/T]AGCTCATTCCATGTC | 11124 |
rs187047146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50722189 | AACAACTTACTGAGC[A/G]TCTACAAGGGCCAAA | 11124 |
rs187050313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50677120 | AATAATATTATTAAG[A/G]TAAACCCATACACAA | 11124 |
rs187059175 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50655206 | TTTGTGTTTTCAGTA[A/G]AGATGGGGTTTCACC | 11124 |
rs187062602 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50530278 | GTGTGTGTGTGTGTA[G/T]GTATATATGTATATA | 11124 |
rs187071653 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50743306 | TGAACCAAAAGTTGA[A/C]GTTTTTATATTTTTA | 11124 |
rs187082198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447883 | CAAGGCTGTACATTA[C/T]CTAATGTTATCAGGA | 11124 |
rs187086538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469627 | AGAGATCATCAAAGC[C/T]GTTTAAAAAAATCAC | 11124 |
rs187095040 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50618894 | GCTGGGATTACAGGC[A/G]TGCACCACCATACCA | 11124 |
rs187095296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50935630 | CACCCACCACCACGC[C/T]CCCAGCTAATTTTTG | 11124 |
rs187098084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495556 | GGCTACTGTGAACAA[C/T]GCTGCAACAAATATG | 11124 |
rs187100703 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50900739 | GTTTCCAATATAAAT[C/T]GTCATTTTTTATAAA | 11124 |
rs187126683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451253 | AAAGTAAGAGAGGAA[C/T]AGAAATTGTGCCTTG | 11124 |
rs187128066 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50513186 | TCTATGTGATAAAAA[C/T]GAATTCTCACTGGCT | 11124 |
rs187128165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543496 | AAATAACACTTACCT[A/T]TAAAACACTTGTCTT | 11124 |
rs187131996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50492477 | CTGAAATGATTATAC[C/T]ATCTGCCCATATTTA | 11124 |
rs187154068 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50837934 | ATTTTTAGCAGAGAC[A/G]GGGTTTCACCGTGTT | 11124 |
rs187158387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726889 | TAGACATTTTCATCA[C/T]TTACTAGACCGTGAC | 11124 |
rs187161099 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50796047 | CTTCACCAGGTAAAA[A/C]AACAACAACAACAAA | 11124 |
rs187167739 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50763851 | CAGGTTTTACATTGC[A/G]ATAAACTTTTAAGAA | 11124 |
rs187178141 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50802336 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 11124 |
rs187184312 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50844423 | TTCACTTTTTCTTGC[A/T]AAACCTGTACATAAT | 11124 |
rs187188320 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50900252 | TCTAAACTAACTTAA[C/T]GAAGACTAAAAGCTT | 11124 |
rs187197985 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50659519 | TTCATCTTTAGAGTA[A/T]GTTAAATTCCAGTTA | 11124 |
rs187210045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50868163 | ATGATACAAGGGACT[C/T]TGGGGACTTGAGGGG | 11124 |
rs187211451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50763265 | TCCATCTCAAAAAAT[A/G]AATACATAAAATATA | 11124 |
rs187213158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50696326 | TCTTTCCTTGTTTTG[A/G]AGGGAGAAAATGTTC | 11124 |
rs187231159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736771 | AAAAGAAAGAAAGAA[A/G]AAAAAAAGATGTCAA | 11124 |
rs187235777 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50806733 | GGTGTCAGGCCCCTA[A/G]AGTGAGAGCATGAAG | 11124 |
rs187241912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50888008 | ATTCTTCCTATCCAT[A/G]AGCATGGAATGTTCT | 11124 |
rs187247931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50912345 | CAGACTTTCTAGAAG[C/T]AGGATTCTAGAATCT | 11124 |
rs187255399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50873090 | CAAGACCCTTCACCA[A/G]CAAAAAGATTAATAC | 11124 |
rs187258829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50850548 | GAGAGAAACTGAGTA[C/T]ATGCACAAGAGATGA | 11124 |
rs187261608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895586 | AACAAATAACAAACA[A/C]ACAAACAAAAAACTA | 11124 |
rs187293601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50566588 | TGGATGTATTGTTGG[C/T]TGTGTGCAAAAGAAT | 11124 |
rs187302314 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656729 | CTCTATGAAAAATAC[A/C]AAAATTAGCCAGGTG | 11124 |
rs187327276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779158 | TTCAGTCACGTCTTC[A/C]GGCTCCTCTTCTAAT | 11124 |
rs187330027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50472902 | AGAGAATTCAGAGAA[C/G]AATGAAGGGCCTTTA | 11124 |
rs187331513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516512 | CCGAAATACCAAGCA[C/T]GCATTTTACCAACTA | 11124 |
rs187334289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734284 | TGTTTATCCATGAAA[A/G]TCTACTATAATCGAG | 11124 |
rs187335896 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50753662 | TTCAACTGGGTCATT[A/T]CTACATTTCCAATGC | 11124 |
rs187336026 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50804568 | GAGGCCTAAGGTTAT[C/T]AGACATAGTTTAAAA | 11124 |
rs187340728 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770880 | ACAAGGCTGCAGTAA[A/C/G]CATAACAGCACGTTA | 11124 |
rs187343788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820981 | TTGGTCATGTTACTA[A/C]TCTAAGATTTGTGGT | 11124 |
rs187373572 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50640251 | AAATATCTGGTAGTG[C/T]TTGGCAATGTAATAA | 11124 |
rs187378655 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50540223 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 11124 |
rs187381248 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50476093 | TATATTTGAGAAATA[C/T]AAGTAGAAGTAACTG | 11124 |
rs187382125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513510 | AAAAAGAATTCCCTA[A/G]CCCTAGGCCTAACTT | 11124 |
rs187384717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50599300 | GTATCTTTGTAGAGA[C/T]GGGGTTTTAACACGT | 11124 |
rs187389319 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | FAF1 | GRCh38.p7 | 1:50493057 | TTTTTTTTTGAGGGG[A/G]AGTCTTGCTCTGTCA | 11124 |
rs187394579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585460 | ATGCTCTGTTTATTT[A/T]GTTTTCAGCAACATC | 11124 |
rs187396700 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50635627 | GATGGAGTTTCACCA[G/T]GTTGCCCAGGCTTGT | 11124 |
rs187400540 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50603532 | GAGGTAGTTTTAAAC[A/C]GAACTGAGTCATGAG | 11124 |
rs187408864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50563286 | TTTAAGAAATTAGAA[C/T]GGGGCATGGTGTCAC | 11124 |
rs187414736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50522072 | TCTTTTTAAAAGTGA[A/G]CATTATTCCATGCAC | 11124 |
rs187415334 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50679911 | AAATTCACAATATAT[A/T]CAATTTCTGGTAAAT | 11124 |
rs187415495 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50884364 | ACTAAAAAAAAAGAA[A/G]AAAAAAATACAAAAT | 11124 |
rs187418862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50717631 | AATCCAAATTGAAAT[A/C]TCACTCACTAAAATC | 11124 |
rs187426632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50746188 | CATTCAAGATGTTGC[C/T]TGGCTGCTTCTAGTA | 11124 |
rs187427534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625829 | AAACCACTGAGAGAT[C/T]TGAAGCAAGCAAGTA | 11124 |
rs187428134 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50846662 | GGCGGGTATTTCCTG[A/G]TGAATTTTTATGCAC | 11124 |
rs187433639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50946275 | AAGTTGTTACACTGG[A/G]GAGGATTTGAGGGTG | 11124 |
rs187436684 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50781001 | CCAAGGCAGCTTAGC[A/T]GATTGCCAACTCACT | 11124 |
rs187437696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50487203 | TCTCATTGCTAGAAA[A/T]TGTGGAAAAATTCTG | 11124 |
rs187452187 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50443524 | CACTTGTTTACAGCC[A/T]TATGGTTAATAAGTG | 11124 |
rs187452993 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50926616 | AAGTTTAAGGTGAAG[G/T]ATATGCTAATTACTC | 11124 |
rs187453789 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50910773 | CGATTTTCCAGGTAC[C/G]GTCTGTCACAGCTTC | 11124 |
rs187458588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945552 | TCGTCATATCCAATA[C/T]AATGAATATGGCTCT | 11124 |
rs187465088 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50823103 | TAAGGGTTTATGAGT[G/T]AGACATCCCGCAGTA | 11124 |
rs187466233 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50533337 | CTTGGCCTCCCAAAG[C/T]GTTGGGATTACAGGT | 11124 |
rs187472586 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50878659 | AAGCAATTTACAGTA[C/G]CTTTTAATCCTCTCA | 11124 |
rs187475105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909763 | ACGCTGTTTATTCTG[G/T]TTAGCCATTCGTCTA | 11124 |
rs187477501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892023 | AGTTCGAGCTTCCCC[A/G]CCACTTTGTTTACCT | 11124 |
rs187485473 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569433 | ACCCAATAGCAATGG[C/T]AATGTAAAATCAGTT | 11124 |
rs187515468 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50610646 | TCCCCACAAAGTGTC[A/G]CTGAGATAATTACTG | 11124 |
rs187521076 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50697969 | ACACATTAGACAAAA[C/G]AAAAATTACCATAAC | 11124 |
rs187529087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681907 | AGTGCAATCTGGGCT[C/T]ATTGCAACTTCCACC | 11124 |
rs187531910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50718492 | ATAAAGTACTAACAT[C/T]AATACAGTGATTGAA | 11124 |
rs187532702 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50650595 | ACCGCACTCCACCCT[A/G]GGTGACAGAGCAAGA | 11124 |
rs187534179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689866 | GCCTATGTAGGGAGA[C/G]GTAATACAACAAAAA | 11124 |
rs187535764 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50718086 | GTGCAATGGTGTGGT[C/T]TCGACTCACTGCAAC | 11124 |
rs187547777 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50755936 | CAGGGACCCTGGGTC[C/G]AGCCCACGAAACCAC | 11124 |
rs187554750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50443890 | TCTTGTTTCTTCCCC[A/G]CGGCCCAGCAAGAGT | 11124 |
rs187555625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50798149 | TAAATGGAAATTAGA[A/C]AAAGCAATACATAGA | 11124 |
rs187573043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466929 | GTTCTCCTCATAACA[A/G]TCTACCAAAAAATCC | 11124 |
rs187584351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50487843 | GTGTTGCTGTGAAAA[A/G]TCAGGTGACCCGGCT | 11124 |
rs187585610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50544271 | AGTATATGACTAAGC[C/T]AGGGGAAACTAAGGT | 11124 |
rs187587839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50519860 | GCTTTAAAAAATTTG[C/T]CCTGGTGAGGCCTAA | 11124 |
rs187596789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497426 | TAAAGGAAGTCTTTC[A/G]GGTAAAAGGAAAAGG | 11124 |
rs187601693 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50588429 | ATGATCCTTGTATTC[C/T]TGCAAAGGTGTCTGT | 11124 |
rs187612160 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50567594 | AGAAATATTAACTTT[G/T]AACTGTTCAACAATA | 11124 |
rs187635547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50608581 | ACGGATGAGGGGACC[C/T]GCTGTCCTAGGAGGG | 11124 |
rs187641712 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50868543 | ATGTAAGCATTTATA[C/G]CTGTAAATTTACCTC | 11124 |
rs187641724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50629827 | ACTTTGGGAGGCCGA[C/G]ACAGGCAGATCACCT | 11124 |
rs187647546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50847191 | GACTGCATAATCATG[C/T]AGAAATAAAAATTGA | 11124 |
rs187651580 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465369 | AGTTCCTAGCACTTT[A/T]ACATATAATGGGAAC | 11124 |
rs187661269 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50455306 | CTGGTTCTGAATTAT[C/T]AAGCAACATTTTCAA | 11124 |
rs187665427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949315 | ATTAGTTTAAATCAG[A/G]ATTCTCCAATACTGT | 11124 |
rs187668487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469319 | GACCTCATGTTCCCC[A/G]TCTGCTGAATGATAT | 11124 |
rs187675144 | snp | A/C/T | 0.00438476 | 0.0466401 | intron-variant | FAF1 | GRCh38.p7 | 1:50498798 | GAGGTTGCAGTGAAC[A/C/T]GAGATCGTGCCACTG | 11124 |
rs187681851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922972 | AAACACAAAAGATCA[C/T]TGCAGGATATTATGA | 11124 |
rs187697672 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50927024 | ATAAAAGAACAAACA[C/G]TAAATAATTCCACGT | 11124 |
rs187697908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50506831 | CAAGAGAAAAAAGGA[A/G]AAAAAGCTAAGGTAC | 11124 |
rs187698383 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768967 | TGAAGGAAACTGAGA[A/C]ATAAAAAAATATACA | 11124 |
rs187700875 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50792220 | CAGCTCAGGTCATGA[C/T]AAGATAGCTACAAAA | 11124 |
rs187702168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486692 | CCCTCTTGCATTAGA[C/T]AGTAAGCTCCTTGAG | 11124 |
rs187706866 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50887862 | TCTTGGCAAGGCAGG[A/C]TCTTTTTTGGTTCCA | 11124 |
rs187708064 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50442721 | CATGGAGGGGTGGGG[G/T]ATATGGGGAAGTGGA | 11124 |
rs187708336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892357 | CTTGGTGCGCTGCAC[C/G]CACTGTCCGACAAGC | 11124 |
rs187708919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636601 | CCTCAGGTGATCCAC[C/T]TGCCTTGGCCTCCCA | 11124 |
rs187710518 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465965 | CCAGCAAGTTAGATC[A/G]AGAAAGGCCTTTCAC | 11124 |
rs187714465 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50811753 | GCCTGAGTAGCCAAG[A/T]CAATCCTAAGCAAAA | 11124 |
rs187716131 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50594696 | GCCAATATAGTGAAA[C/T]CCCGTCTCTATTAAA | 11124 |
rs187718986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50850223 | GGTAGAAATACATAC[A/G]GCATGTCTGAGAATA | 11124 |
rs187719703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50829040 | GGCTATTAATAATCT[A/G]GGAAGTATAATTTAA | 11124 |
rs187727618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50507622 | CTCAGGAAGCTGAGG[G/T]GGGAGGCTGTTTGAG | 11124 |
rs187729639 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50858603 | TCATTAATAATTTTT[A/C]CTCTGAATACATGTT | 11124 |
rs187736438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50530827 | AACAAAAAACAAACT[A/G]CAACAGAAGCCAGAA | 11124 |
rs187744551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909174 | TCTGGGTTGAAAATT[A/C]TTTTCTTTAAGAATG | 11124 |
rs187755336 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50891329 | TTAGCCCAGAGAAGT[G/T]TGGTCTTCTGAAGCC | 11124 |
rs187755800 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50676714 | GTGATCTTAGCTACT[C/T]GGGAGGCTGAGGCAG | 11124 |
rs187757191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632451 | TATGCTTGTTCATCA[A/G]TAAATCAGGAACACA | 11124 |
rs187761015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50712764 | TAACTATGTGTTGAG[C/T]CCTCAGCTGCAGCAT | 11124 |
rs187761429 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50590539 | GTTCCAATAGTTTTT[A/T]AAAAATGTAATCTTT | 11124 |
rs187761943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876435 | ACGAACCTGGAACAC[C/G]TTGTAGTGCCAGAAT | 11124 |
rs187768832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50672107 | CTGGAGTACAGTGGC[A/G]CGATCTCAGCTCACT | 11124 |
rs187769313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50856819 | ATACCCAACAGCATA[A/G]GACTAGTTGGTTAAT | 11124 |
rs187777280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50839098 | AGAGAAGTTTTCTTC[A/C]TAAAAATAAATATAT | 11124 |
rs187783857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50737350 | AATCCATTTAATCAC[A/G]CTACTGGAAAGCAAC | 11124 |
rs187804225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708195 | GCTGCTCTGGCCACA[A/G]TGAGCAAAGACTGGG | 11124 |
rs187810943 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50774701 | CACTGATTTAACAAA[C/G]TTTATTAAACAAATA | 11124 |
rs187822711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50817073 | AGTACCATGGCGTTA[C/T]GGTTACTTTAGTCTT | 11124 |
rs187827255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816147 | TTGTTGGCCATTATA[C/T]GTCTTATTTTGAGAA | 11124 |
rs187837916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952390 | GTCAAGATTGCAGAC[A/G]GAGTCTCGCTCACTC | 11124 |
rs187850672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50776455 | TAATATATTTAAAGT[A/G]TAACATTAACATACA | 11124 |
rs187856622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937582 | CTGGGACTTTGTACC[A/G]TATGATTCTCATGGT | 11124 |
rs187861622 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50799768 | CTGCATATATTCGAC[A/T]TTATTATAAAAACCA | 11124 |
rs187873712 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50817521 | TGTTTAATGGGTACA[G/T]GGTTTCAGTTTTAAA | 11124 |
rs187880160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836318 | TGGGTATAATAGCAT[A/G]AGTCACCATGCCCAG | 11124 |
rs187896480 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50630486 | CCTAAATATAACCGT[C/T]TTTTAACATGCAGTC | 11124 |
rs187904751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50650208 | AGAATCGTTTGAATC[C/T]GGAAAGCAGAGGCTG | 11124 |
rs187921035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50491573 | ACCATGCTTTAATAA[A/C]CATGGATAGGATTAT | 11124 |
rs187924518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671086 | TTTATAATCATCAAA[C/T]AGTCTAAACATTCTT | 11124 |
rs187934351 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50707360 | CACACCCAACTAAAA[C/T]AGAATTTCTTGAAGC | 11124 |
rs187934520 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50503399 | GCAAAGGTAGAATTG[C/T]TTGAGGCTAAGAGTT | 11124 |
rs187937964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50689615 | AAAACAAAACAAAAC[A/G]TATGTCCAAACAAAA | 11124 |
rs187940364 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50539821 | TGTGTTATTAGTTAT[G/T]TTAAATTAGACAGCC | 11124 |
rs187943021 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1 | GRCh38.p7 | 1:50447326 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 11124 |
rs187943338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50727633 | GTGATGGTTAATATC[A/G]GGTGTCAACTTGATT | 11124 |
rs187954458 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50930510 | TACAATGGTAATAAC[A/G]ACAATCTTGCAAAGC | 11124 |
rs187959782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50903690 | TTGCTAACCAACCAC[A/T]TTAGTGATATTGTAA | 11124 |
rs187961793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921111 | CCCACTGTGTCCCCC[A/C]AAAAATCAAACATAC | 11124 |
rs187965005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895879 | AGCCTCAACACACTG[C/G]GTATAGAGAGAACAT | 11124 |
rs187966328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748221 | AAGAAAAATGCCAGG[C/T]GTGGTGGCTCATGCC | 11124 |
rs187973708 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50886284 | GGTGTTGATGAAATC[A/C]CTCCGCTTTTCTTTG | 11124 |
rs187976565 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50584899 | TAACAACAGGACATA[A/C]GCGTTATAAAATTTT | 11124 |
rs187981575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870194 | GGGCACATTGGCTCA[C/T]GCCTATAATCCTAGC | 11124 |
rs187983010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50863583 | ACAAAAAGCTGCTTC[C/T]TTGAAAAGATGAACA | 11124 |
rs187985753 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50497840 | GGTGTGTGCCACCGC[A/G]CCCGGGCTCAAAACT | 11124 |
rs187987418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50664780 | GACTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 11124 |
rs187991180 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50905455 | GATCCTTGAGGAATC[A/G]CCACACTGTCTTCCA | 11124 |
rs187993692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50615578 | ATTTTGTCTGGTGTG[A/G]GATGGTATCTCATTG | 11124 |
rs187993855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50625326 | CATTCTTCTCTAATC[A/G]TCCTGTCAACAAATA | 11124 |
rs187994300 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50474468 | TATTTGGTTACATGA[C/G]TAAGTTCTTTAGTGG | 11124 |
rs188000779 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50454201 | TGCTTACTATGCTGA[C/T]CTCTAAATATTATCC | 11124 |
rs188001565 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872625 | AAACAGGCTGGGCGC[A/C/G]GTGGCTCATGCCTAT | 11124 |
rs188025207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521036 | ACTGTTTTTTATATA[C/T]TAATTCATTATTTTT | 11124 |
rs188028264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50693284 | TGTGCATGTAGATAT[C/T]TAGTTGTCCCAGCAC | 11124 |
rs188034356 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50654459 | GATGGCCTCCTTATA[A/T]AATGAAATTTACTCT | 11124 |
rs188041085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50694017 | TATATATACATGACA[C/T]ATATGACATATATAT | 11124 |
rs188045100 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50733895 | TCCACCTCCAGGGTT[C/G]AAGCAATTCTCCTGC | 11124 |
rs188056117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601759 | ATTCATATATACACA[C/T]ATATATTCATATGTA | 11124 |
rs188071745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50769870 | AGCCTGGCCAATATG[A/G]TGAAACCCCATCTCT | 11124 |
rs188082129 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50812043 | TGGGCCCCTTCCATA[A/C]AGCATATACAAAAAT | 11124 |
rs188109139 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50835514 | AGGCGGGGGTTGCAG[C/T]GAGCCGACATTGCGC | 11124 |
rs188115474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50809656 | AAAAGGCCAGGACCA[A/G]ACACAGTCATTCACA | 11124 |
rs188134492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751157 | TTTCATGTTAAAAAA[A/G]AAAAAGAGCTAAACT | 11124 |
rs188151523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50840254 | AAAATAATTCATAAA[C/T]TGAATTTTATTCAAG | 11124 |
rs188154146 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50767796 | AGACACTCCTTAAGG[G/T]TGTGCTAAATATGGA | 11124 |
rs188155794 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50789941 | TCCCTCTAAGAATAT[A/C]CTTTCCTCCATTACC | 11124 |
rs188163991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581807 | TAAGATTATGGGGCA[A/G]TACAAATGGTACACT | 11124 |
rs188171100 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50810872 | TGGCCAACATGGTGA[C/G]ACCCCGTCTCTACTG | 11124 |
rs188177001 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50827652 | AATAAATAAATAAAT[A/C]AATAAATAAATTCCA | 11124 |
rs188179729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50524367 | GATGTGTGTTTTGCT[C/T]TGCAGAAGGTATTTA | 11124 |
rs188189473 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50941366 | AGGTGCCAGCCACCA[C/T]GCCCAGCTAATTTTT | 11124 |
rs188191481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50643407 | ATTGCTTATTAATTT[C/T]TTTCCTAAAATTTAT | 11124 |
rs188193932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50478828 | TGTATAAAGCTTTAT[C/T]CTTTCTGTTCAAAAT | 11124 |
rs188194561 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50932530 | AAAGGTGGGTTCCCA[C/T]GGTCTTGGGCAGCTC | 11124 |
rs188201161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50950298 | GCCCCTTATGGAGGT[A/G]TAACCACATATTGCC | 11124 |
rs188203692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601654 | GCCGCTGCACTCCAG[C/G]CTGGGTGAGACTCAG | 11124 |
rs188211057 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50573729 | ACTTTCTGAGCAGAT[G/T]TTGGGATAGCATTCT | 11124 |
rs188211343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50448372 | TTATAAAATTGAGAC[C/T]TTTTTTTTGCCTCCC | 11124 |
rs188214500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50623374 | TGAGTTCGAAACCAG[C/G]CTGGGCAACATGGCG | 11124 |
rs188214711 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683013 | ACTCCAGCCTGGTGA[C/T]AGAGCAAGACTCCGT | 11124 |
rs188215555 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50916410 | CATTACCATTCCCTT[G/T]AGGACTTATCTTCAC | 11124 |
rs188217163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949129 | TCAGCAATTCTCAAG[G/T]GTAGTCCTTGGATCA | 11124 |
rs188218745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50906202 | GTAGATGTGTGGTAT[C/T]ATTTCTGAGGGCTCT | 11124 |
rs188222323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50899583 | TCAGCCTCCCGAGTA[A/G]CTGGGAATACAGGCG | 11124 |
rs188223049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50480691 | ACTGTATAAACCATG[C/G]AGGTCTCGTAAGATT | 11124 |
rs188227883 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50662338 | TTCTTCATTCTAATA[A/C]CTGTAACTTAGTTTT | 11124 |
rs188230056 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50699262 | TAAGAACTAATTATT[C/T]CACAGTCTTAGTATT | 11124 |
rs188231256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50913868 | CCAAACCAATGCAGG[C/T]AATTTGTTCTGTTTC | 11124 |
rs188248149 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50719887 | TGGGTTTGGTACCTC[A/G]CTCCAATTAGATGTG | 11124 |
rs188249228 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50615340 | TGAATAGCACTGCAA[A/G]TGTCATTTTGGTACA | 11124 |
rs188249341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603272 | CCATACATGACAACT[C/T]TGTAAATTAAAGACT | 11124 |
rs188251065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881612 | ATACTTCCATACATG[A/T]CAGTAAGTTGAAAGT | 11124 |
rs188252160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50882011 | CACACAAAAGGCATT[C/G]TTTCAATACCCATGA | 11124 |
rs188252178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526518 | TGTGTGGCCCAGGCT[C/G]GTCTTAAACTCCTGA | 11124 |
rs188255674 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50645898 | AAAATACTATTGACA[A/C]AAACAGATGCTGAGT | 11124 |
rs188258096 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50563147 | AGGAGGTCCTGGAAC[C/T]AATCCTGCATAACTA | 11124 |
rs188265993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50843529 | CCAACCTCTCTTCAT[C/T]CCCCGCTCCCTACCA | 11124 |
rs188281747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50685942 | ATAAATGATACATGA[C/T]AATTTCCCCATTGAG | 11124 |
rs188288098 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50645540 | CATTAAGAAATCAAT[A/G]TGGCCAGGCGCTATG | 11124 |
rs188315786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760442 | ATAGATGGAAGTAAA[C/G]CTCTCCTCTGCAAAT | 11124 |
rs188317426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50714165 | CTCTTCACTGGTATA[A/G]ATATTTTTTTTCTTC | 11124 |
rs188338934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50752784 | GCCTCCCGGGTTCAA[A/G]TGATTCTCCCGCCTC | 11124 |
rs188358677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50794289 | AAATTTGGACTGGGA[A/G]GAGAAAAAATGATTA | 11124 |
rs188361823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50793641 | GTGTTTTATTTTCTA[C/T]ACTAATTTGTAAGCA | 11124 |
rs188372028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50830390 | GCTGGGATTACAGGC[A/G]TGAGCCATTGCGCCC | 11124 |
rs188378043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50829189 | AGGAGATAGGTTGTA[A/C]TGACAACCACTTTCA | 11124 |
rs188415813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528001 | TTAGCCTCCCGAGTC[A/G]CTGGGACTACACCAC | 11124 |
rs188423123 | snp | G/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462954 | TTAACACAGCAGGAC[G/T]GCTACTGTTTGAGAG | 11124 |
rs188423191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505187 | AATGGTTAAATACCA[C/G]AACTGGGACCTAATC | 11124 |
rs188425878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50473435 | GACTTAAAACTAAGG[A/G]TTGGGAAGGGCAAAC | 11124 |
rs188429560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50484431 | ACTGAAAGTACTGAA[G/T]AAATAGTGGATATAC | 11124 |
rs188441088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598119 | GGCAACATAGTGAGA[C/T]CTTGTCTCTAAAAAC | 11124 |
rs188443175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50604421 | AACTGAGGTATAGAG[A/G]GGTAAAGTGTTTGTC | 11124 |
rs188447008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576516 | TTGATTTTTAGTTAC[C/T]ATAAATGTCTAATGA | 11124 |
rs188449223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50553358 | GTCTAGGAACCGAGA[A/G]GATTATCAAGAATGA | 11124 |
rs188475240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50500558 | GTGAAGTCTAAAGCT[A/G]TAATACTTATAAAGG | 11124 |
rs188481722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560257 | GACAGCTTACTGATA[A/G]TAAGTGCTTTAAGTC | 11124 |
rs188485061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956877 | CACTTGAACCCGAGA[A/G]GCGGAGGTTGCAGTG | 11124 |
rs188493547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50509270 | CTTTCCACATCTAAA[C/G]TATAAATGATGAGGG | 11124 |
rs188494983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50699705 | TCTCTGCTTCAATGC[C/T]ATTAGAATGAGCCTT | 11124 |
rs188495108 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50593808 | TCAATTACATAACTC[C/T]ATTTCTCTTTCACAT | 11124 |
rs188499176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923165 | AACGCACACCTATAA[C/T]CTCAATGCTTTGAGA | 11124 |
rs188501650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550307 | AGTGAATCGAGATCG[C/T]GCCCCTGCACTCCAG | 11124 |
rs188502014 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50600563 | ATAAGACTAACCTTT[A/G]GGAAACTACCACTTC | 11124 |
rs188502374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471474 | TGTTCCTTTAAGTCT[C/T]AGAGGGAGAAACAAA | 11124 |
rs188505044 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50720775 | AGACAGATGATCACC[G/T]CTTCTTCTGAGAGCT | 11124 |
rs188506451 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50867533 | TAGGGACATGAATAG[A/C]CAATTCTCAAAAGAA | 11124 |
rs188507930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50858208 | CATTGCTCTGAAAAA[A/C]AGACAATAAAGCAGG | 11124 |
rs188509377 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470119 | TGAAAATCAATCCCA[C/T]TGCAATATTAGAGGT | 11124 |
rs188512405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50888310 | CTAAATATACAATCA[C/T]GTCATCTGCAAACAG | 11124 |
rs188516601 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846138 | GAAAGGAAAAGAAAC[A/G/T]AAAAAGGAAAGAAAG | 11124 |
rs188522738 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50515605 | AGATAGGAACAAAGT[A/G]AGTAAGCAAATGTCA | 11124 |
rs188522813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874025 | AGAAATGATGCAGGG[C/T]ATGTGAGACCCAAAA | 11124 |
rs188527409 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50740930 | CATTTGATCATTATT[C/G]TTCTTTTTCCATGCC | 11124 |
rs188533785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50757632 | TTAGTTTTTATTCAA[C/T]TTCTATACTTTATAA | 11124 |
rs188536086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50670573 | ATAAAGGTAGAAATA[C/T]TGCAGTTAAATTAAT | 11124 |
rs188537482 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50777723 | TTCAAAATGAACTTT[C/G]GAACCTGAATTCATT | 11124 |
rs188542631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863220 | AAAGAAACCCTCAAA[A/T]CCATGCAAATACATG | 11124 |
rs188544503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50642166 | CAAGACTGTGCCACT[A/G]CACTTCAGCCTGGGC | 11124 |
rs188545209 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50450098 | ACTCAGGAGGCTGAG[A/G]CAAGAGAATTGCTTG | 11124 |
rs188545862 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800587 | TTAGAAGAGAGGAAC[A/G]GGGGTATAGGTCTAT | 11124 |
rs188550727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50665747 | TGCTGACCCCTAATA[C/T]GGAAGAATATTTGGT | 11124 |
rs188557875 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50818861 | AAAAAAAAAGAAATC[C/T]TGGAGATGGGACCCC | 11124 |
rs188561124 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50541773 | AGAGAGAGAGAGAAG[A/G]GAAATAAAAAAAAAG | 11124 |
rs188581938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50704080 | GTTTAATTTAAAAGG[A/G]TGAAATTAAGTCTCC | 11124 |
rs188588964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50743783 | CTGGAAGAAAAAAAA[A/G]TGTGTAAGCCCAGGT | 11124 |
rs188597981 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50744849 | CATATCCAGAGCTAA[C/T]ACTAATATGTGGCAT | 11124 |
rs188612133 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779742 | TTAAAATAGATTCAT[A/G]TAACTATAAGATGTC | 11124 |
rs188624815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50821335 | TGAGTGCCAGAAATC[A/G]TATTTTTTTACAGGC | 11124 |
rs188645697 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50813259 | AAAATTGAAAAAAAA[A/T]TTCATTTTTTAAATT | 11124 |
rs188695447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50453815 | TGGCCAGCCTTTTCT[C/T]CATGCGTATTCCCTA | 11124 |
rs188708628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598823 | TAAATACAAAAAATT[A/G]GCCGGGCATGGTGGT | 11124 |
rs188718674 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | FAF1 | GRCh38.p7 | 1:50953134 | GTGCTGTGTCCACTC[A/G]GGGTTAAATGGATTA | 11124 |
rs188731092 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50938816 | TTATCCTAGCACCAT[C/T]TATTGAATAAGGGGT | 11124 |
rs188731204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639123 | AAGTATTGTATCTAT[C/T]AGTAGTTTGCTGCTT | 11124 |
rs188737577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50658377 | GTACACACAAATACT[A/G]TAAGTATACAAACAA | 11124 |
rs188738568 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50497739 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATCTT | 11124 |
rs188747910 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50618851 | CCTCCTGGGTTCCAG[C/T]GATTCTTCTGCCTCA | 11124 |
rs188748416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452353 | ATGAGCCCCAGCAGT[A/G]TGCCCAGCTTACAGG | 11124 |
rs188749114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902006 | TTGATTAATGAAATT[A/G]CAAAGTACCTAATTT | 11124 |
rs188755722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50678960 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 11124 |
rs188756099 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50724923 | AAGGCAGGTCTACTG[C/T]ATCAGTCCATCAGGC | 11124 |
rs188758764 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50589843 | TTCATATATTTTGAG[C/T]TTAGTTTTGCATATG | 11124 |
rs188758791 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50925932 | AAAAGAATGGAATTG[G/T]GCCAGATGTAGTGTG | 11124 |
rs188762051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50704933 | ACTGGTTCTTTCAAA[A/G]TGACATTAAGTGATT | 11124 |
rs188763859 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50745642 | ACTTTGCCTTCTGCC[A/G]TGAGTAAAAGCTCCC | 11124 |
rs188764390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869378 | ATTATGGTTGGGCTT[C/G]AGTCTGCCACACTTC | 11124 |
rs188765229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50533766 | ATTAAAAATGATAAT[C/T]TTACCAATATCTGTG | 11124 |
rs188772090 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50695760 | TTCAAGTGATTCTCC[G/T]GTCTCAGCCTCCTGA | 11124 |
rs188774587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545280 | AATTATAGCTACATA[C/T]ATATATATATTCGAG | 11124 |
rs188777120 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50762627 | GGTGCTGGGAAAACT[A/G]GCTAGCCATATGTAG | 11124 |
rs188781646 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779973 | ATATCACTACAAGCA[C/T]ACATGCACAGACAGA | 11124 |
rs188781968 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50877549 | GTAAATATACATTAG[A/G]GTTAGAGCTACCTAC | 11124 |
rs188789019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50649071 | ACAGGTGTGAGCCAC[C/T]GTGTCCAGCCTTCAG | 11124 |
rs188793734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806578 | ACAAATGAACGCAGA[A/G]CCCACTAACCCGCTG | 11124 |
rs188799416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50839390 | GAAGTCTGGTATTAA[C/T]AGACTTTAGTCGCAT | 11124 |
rs188802011 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50822690 | CCAGATTGAATTTGC[A/G]AGCTAAAACCTAAAA | 11124 |
rs188807361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50580155 | ACTGCTAAAAACTAT[C/T]AAAATTTATTTGAAG | 11124 |
rs188811554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50689094 | AAAAAGGTTTTGAAA[A/G]TGGGTTAAAGTGATG | 11124 |
rs188813656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660802 | GCCAGAGAACTAGAT[A/T]TCTAATCCTAGTTCT | 11124 |
rs188818641 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50565664 | TAAAAAAAAGAAACC[C/T]TCAAACACTGTTTTT | 11124 |
rs188823285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50622023 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCAGGT | 11124 |
rs188833101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543005 | TGGTAAGATAAGATG[A/G]AATGGTTTTAATCTA | 11124 |
rs188835230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516163 | AGGATTTGAATTCAG[A/G]CAATATAGCACTGCA | 11124 |
rs188845080 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656704 | CCTGGCCAACATGGC[A/G]AAACCTTGTCTCTAT | 11124 |
rs188845414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606557 | CAGGCTGGAGTGCAA[C/T]GGCACGATCTCAGCT | 11124 |
rs188846531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50628728 | AAAGACCTAGTTACC[A/G]TTTTCATCTCACATT | 11124 |
rs188851439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50698658 | GATATCAATTCATTA[A/G]TGCCTCATTACTTAC | 11124 |
rs188851535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50738649 | ATTATACTGGAGTTA[C/T]GCTAAAGACTTTAAA | 11124 |
rs188854490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50677622 | AATTGGGGCTGGACA[C/T]GGTGGCTGACGCCTG | 11124 |
rs188854668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50587725 | ACGCTGTTTGGACCT[A/G]TGTGGAAGATACAGT | 11124 |
rs188857835 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50764400 | AAAGATTTGCAGAAA[G/T]CATCATTCAGATACC | 11124 |
rs188866891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808188 | AAAAGGATAAATAAG[A/C]TCCTTTTCAGACAAG | 11124 |
rs188870003 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50694567 | AGGAAAAAAAAAAAA[A/C]CCCACAAAGGTCTCC | 11124 |
rs188878417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760996 | TGCAATAAAAAATGA[A/T]AAAGGGGATATCACC | 11124 |
rs188883069 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50647490 | TGCCAATTTGCGAAT[A/C]ATTTTTTTTTCTTGT | 11124 |
rs188884285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931743 | TTAGCCAGGCATAGA[A/G]GCAGGCGCCTGTAGT | 11124 |
rs188887135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462491 | GTTGATCTGTATTTG[C/T]TTATAGTAACAAGCA | 11124 |
rs188887148 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50889882 | GATGTCTATTAGGTC[C/T]GCTTGATGCAGAGCT | 11124 |
rs188888681 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50714808 | CTAATAACTCTAAGC[G/T]CTGTCTATTTTCCAT | 11124 |
rs188891302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875035 | CCTTCCCAGAAGTGT[A/G]AGAAAGTTATACCAC | 11124 |
rs188895221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50915128 | GTAATCCTAGCACTT[C/T]GGAAGGCTGAGGCGG | 11124 |
rs188898120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50805418 | ATAGCACACTAAAAG[A/G]CATGTAAGGTATGCA | 11124 |
rs188899393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50853744 | TGAAGGAGTTTCATA[C/T]CTAGAGACCGTGTGT | 11124 |
rs188903558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50482486 | GTGAAAGCAGTTTAC[A/T]GTTACTTTCATTTCA | 11124 |
rs188907716 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50837643 | TTACTAGATCTAACA[C/T]TGACCTATAAAGTTT | 11124 |
rs188987413 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50446015 | TCCTTTTCTAAAAAG[C/G]CTATCACTGCTGTTG | 11124 |
rs189011155 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50520774 | TGCTTCAGCCTGGGA[G/T]GTCGAGGCTGCAGTG | 11124 |
rs189011233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50919081 | AAGTGTCAGGAATGT[C/T]ATTTCCTTAATAATT | 11124 |
rs189012860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848528 | TCAAAATATTTCCCA[A/C]AAGATACTTACTAAT | 11124 |
rs189019623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945049 | GAAATCGTTGAGTCA[A/G]TTTTTGAAGAAGCTG | 11124 |
rs189026342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50473910 | TATGCTAGGTTACTA[C/T]ACCTAGATCACAATG | 11124 |
rs189028598 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50536132 | TCTTTTTTTGCCCAA[C/T]TGATATTTCTCCCTT | 11124 |
rs189033339 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885340 | CTCTCTCTCTCTCTC[C/T]CTCAATATTTGCTTT | 11124 |
rs189038167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50885878 | TATTGGAGGTTACCA[C/T]GAGGCTTCCAAATAC | 11124 |
rs189038777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50567984 | TGTCTTCTGTCATAG[A/T]TGGATACTCAATGCA | 11124 |
rs189040724 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50489174 | ACTCCTAGACAGGCT[A/G]TATATTCCCTCTAAG | 11124 |
rs189041927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869839 | ATATTTTAAACATAT[C/T]TACCTTAAAGTCTCT | 11124 |
rs189052381 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50848389 | CTAACTGTAGAATCT[C/G]TCTGATTATATTGTG | 11124 |
rs189053933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847971 | ATCTTAAAAAAGGCT[A/G]TCAACACAGAATTCC | 11124 |
rs189064368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570244 | ACAAGCGAATGCAGA[C/T]GGTGAAAAAGAAATA | 11124 |
rs189064776 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50546227 | TTTAAAGAGATACTA[C/T]GTAGCCATTAAATAG | 11124 |
rs189080017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822867 | GCAACCTCTGCCTCT[C/T]GGGTTCAAGCGATTC | 11124 |
rs189081186 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50521200 | ACTATTTTTTTAATG[A/T]CCCCAGAAACAACCA | 11124 |
rs189089647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50612005 | TTGTTTGTAGAAAAT[C/T]ACACATATTGGTGAA | 11124 |
rs189093124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50633947 | GTTGATCACAATTGT[C/G]AACAAACATACAATA | 11124 |
rs189104653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653266 | TATACTATAACATCA[A/G]TGCTAAAATCAGTTT | 11124 |
rs189107333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591222 | ATGTGCTGTATTACA[C/T]TGAGGATTCCATTAT | 11124 |
rs189111926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50682710 | AGTAACTTCAGGTAC[C/T]ATAACTAACAGTAAA | 11124 |
rs189114449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50947993 | GTTGTTTCCCCAACA[A/G]AGCTGACAGTACGAG | 11124 |
rs189120208 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50719573 | ATCAAAATGTATTAA[C/G]CAAAGTATGTAAAAT | 11124 |
rs189122954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50691737 | CTGGCATTATAGGCA[C/T]GCACCACCACGCCCG | 11124 |
rs189124395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927949 | ATATGGATGTGTTCA[A/T]GTTGTGCAAATTCAA | 11124 |
rs189127542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50672739 | TTCTTATTTCATTAT[A/G]GTCCTTGAACTATAA | 11124 |
rs189135885 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50911642 | GCAGAGGTTGCAGTG[A/T]GCCAAGATGTTGCCA | 11124 |
rs189138398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50785431 | TCTATAACTCAACAA[C/T]AAAATATCAAATAAC | 11124 |
rs189145197 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50757118 | GTTGCCAGAACACTT[A/G]TCACTTAATTTAAAC | 11124 |
rs189146724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756669 | AATTTATACAGAAGA[A/C]AGGGTTTAACGGACT | 11124 |
rs189155383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50730031 | TCTCCAAAATAAAAA[A/G]AACAGATTGTGATAA | 11124 |
rs189158943 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50825223 | TGCAACCCATAAATA[C/T]GTACATTATGTGTCA | 11124 |
rs189162594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50799932 | CAAGAGGAATTTTCA[C/G]TTATGTTAAATCCAC | 11124 |
rs189169610 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50726425 | AAATAGGCTGGGCAC[A/G]GTAGCTCACGCCTGT | 11124 |
rs189173858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50754149 | TTTTCTACATCTTTG[C/T]GTGCCTGGTAATTTT | 11124 |
rs189175943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771617 | AAAAACAAAAAATAA[C/T]GGGCCCAGCACACTG | 11124 |
rs189179824 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50837000 | TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 11124 |
rs189183117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50795259 | AAAATATTTCCATCA[G/T]GGAGGGGGCAGTGAT | 11124 |
rs189191668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50746592 | CAGGCATGAGCCACC[A/G]AGCCCGGCCAATGAA | 11124 |
rs189193895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50814491 | AACAAACCAACTACA[A/G]ATACATTCATCTACA | 11124 |
rs189204531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50830618 | TATTAGTTTATCAAA[C/T]AGATTAGCCAGTGTA | 11124 |
rs189231481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50458152 | TGGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGATT | 11124 |
rs189234135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50958812 | ACCTGTGCAATGTGA[A/G]TATTAAAAAAGAGGG | 11124 |
rs189236360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50923948 | AACCCATATATGACA[C/T]ACCCACAGCTAGCAT | 11124 |
rs189236570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50953800 | CAGCAAAAAGTATTA[C/T]TAGCTGAAAAGACTA | 11124 |
rs189263504 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50889670 | TTCCATGTAGTTGAG[C/T]AGTTTTGAGTGAGTT | 11124 |
rs189277954 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50852562 | GTAGGAAGAAAAAAG[C/T]CAGTACAGAGAAGAA | 11124 |
rs189280323 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50514954 | TAGATCCGGTCATCA[C/T]TAACTCACAGATTAT | 11124 |
rs189281864 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468419 | TGCCTCAGCCTCCCA[A/G]GTAGATGGGATTACA | 11124 |
rs189298352 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470917 | TCCTTTATAATACTT[A/G/T]CCGTTATCACAGCCT | 11124 |
rs189304908 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441105 | CTGTCCTAGACACTG[C/T]GGGGAAAAGATGGGC | 11124 |
rs189314105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510919 | GTGTCAAGTACATAG[G/T]TGTTTACTTTATTTT | 11124 |
rs189316396 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50563899 | GTTATTAGAATCATT[C/T]AAGAGGTGTAAAAAT | 11124 |
rs189346720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50561511 | TAGAGATGATTTATT[A/G]TCAATATAGTACTTA | 11124 |
rs189369734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50638515 | AGTGGCGCAATCTCC[A/G]CTCACTGCAACTTCT | 11124 |
rs189373433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708622 | GTCAGTTTTTAGGCT[C/T]CGAGGCCAAAACAAA | 11124 |
rs189374092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50652871 | GTCGACTCATTTACT[A/G]AGTGTCTACTATGAG | 11124 |
rs189388625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50673030 | TGGGAGGCTGAAGCA[A/G]GTGGATTACCTGAGG | 11124 |
rs189403971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749920 | AAAATGTTTTGCAGA[A/G]TGCCTAATACATACT | 11124 |
rs189407228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50690861 | TGTGTTTAGTTTCTT[C/T]CATTTAGCATGTTTT | 11124 |
rs189410709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50927519 | GGCACTCTGCCTGGG[C/T]GGCAGAGTGAGACCC | 11124 |
rs189411178 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50739310 | TGTGTACACGTACAT[A/G]CATATACATGTGTAC | 11124 |
rs189413649 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729046 | TATCTATATATATAT[A/C]TATATATATATATTT | 11124 |
rs189414381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50911129 | TCATGCTGGAGTGCA[C/G]TGGTGTGATCTCAGC | 11124 |
rs189416856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50673970 | GCTTTTTTTTTTTTG[A/G]CATGGAGTCTTGCTC | 11124 |
rs189417758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709749 | CCTGCTAGAAGTTTA[A/C]CGCTCATTCATTCAC | 11124 |
rs189418216 | snp | A/G | 3.29761e-05 | 0.00406041 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788119 | ATTACAGGTCGAAAC[A/G]CTGAAGAAGAAGAGG | 11124 |
rs189419174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50893359 | TATTGGAAAGAACTT[C/T]GGTGTTGTGATCTAA | 11124 |
rs189422524 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50710092 | GGGCTTCAAATGCTA[C/G]GCTGAGGAGCTCGGA | 11124 |
rs189423581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50750570 | TAAAGATTACTTTTG[C/T]CTGGGTTCCTTTGTT | 11124 |
rs189433686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777240 | AACAAAATGAGACCC[C/T]ATTTCTTCAAAAAGT | 11124 |
rs189434766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50879072 | CCAACATGGTGAAAC[A/C]CCGTCTCTCCTAGAA | 11124 |
rs189439440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50766994 | AAAATGACAGAAACA[C/G]AATTCAGAATATGGA | 11124 |
rs189441089 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50859884 | AAAACAGCATGGAAT[C/T]GATACAAAAACAGAC | 11124 |
rs189444299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50535115 | TAATTTCTTGCAAAT[C/T]GACTTCCTGTACCCA | 11124 |
rs189448465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841360 | TATGTACACATGCTT[A/G]TATATAGATCCCAGG | 11124 |
rs189453566 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50818216 | AAACACACTAAAGTG[A/C]GTGAAATTAAAAAGA | 11124 |
rs189456715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510053 | GTGCACCTGTAGTCC[C/T]AGCTGCTCAGGAGGC | 11124 |
rs189460802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467295 | TCCAAATATGTAACA[C/T]TGAGCTTCATTTACA | 11124 |
rs189464836 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50488657 | TAGGGTTTTGTACTG[A/G]AATGGAGTATGAGAA | 11124 |
rs189478378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601511 | ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 11124 |
rs189484780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50580944 | GCCTGGCTAATTTTT[C/G]TATGATTTTTTGTAA | 11124 |
rs189488886 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50560804 | TCAGAACAAGAGATA[C/T]CCACTAACCCACTTA | 11124 |
rs189504127 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50932370 | GGTATTGGGTAAACA[C/T]AGCCATTCTACATGG | 11124 |
rs189508732 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50898643 | GCATTCTCCAGGACA[A/G]ACCACAAAAAACTAT | 11124 |
rs189521884 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50448639 | TGTCCAGCTATACCA[G/T]GGACTGAGTGGGCAA | 11124 |
rs189524278 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865138 | CAAAACCACAATGAG[G/T]TACCATCTCACACCA | 11124 |
rs189532699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50906792 | GGGCTGAGACGATGG[A/G]GTTTTCTAAATACAC | 11124 |
rs189535715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862560 | AATACTAACATCAAA[C/T]GTAAATGGCCTAAAT | 11124 |
rs189542022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842689 | TTCTGTTTTCACCTG[A/G]CTGGCTCCTCGTTCT | 11124 |
rs189551278 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874495 | GCTCCCAAGTAGCTA[C/G]GACTACAGGCGAGCA | 11124 |
rs189554441 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460029 | TAGAATATACTCATT[C/T]TTCCATGTATAGTTC | 11124 |
rs189570967 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50494045 | CTTACTCACAGCTCT[C/T]TCTGACCATCCTGAC | 11124 |
rs189577696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50586136 | ATTTTAAAGCTGGAA[A/G]GATCTTAAAAATCTG | 11124 |
rs189592260 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50585897 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAAGTCT | 11124 |
rs189599806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541054 | TTTGAAAAGACAAAC[A/G]GCATTAAAATGTCAT | 11124 |
rs189602884 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50628208 | AGATCAAAGAAAAAA[C/T]ATATTAGATATTATT | 11124 |
rs189611847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50801488 | AATTAATATAACACA[C/T]AGAAATATCTGAAAG | 11124 |
rs189617511 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50819705 | TACATATATATATAC[A/G]TATATATATACGTAT | 11124 |
rs189635143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667371 | TACTTGGCCAATGGA[C/T]AGTAAATCAATTATG | 11124 |
rs189638933 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50656971 | ATCCCAGAATTTTAG[A/G]AGGTCAAGGTACAAG | 11124 |
rs189643203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949860 | TAGCTCTACACAGAT[C/T]ACCATTCTTTTTTTT | 11124 |
rs189644887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50907049 | ATTATCTTGAGATAC[A/G]TCCCATCAACACCTA | 11124 |
rs189648783 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50618680 | ACCCTTTATCATTAC[A/C]TAAGGCCCTTTATTG | 11124 |
rs189651527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50625211 | GGCAGAGAATCCTAC[A/G]CTCTTAACAACAATA | 11124 |
rs189665240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50690563 | CTGAGATCGTGCCAC[C/T]GCACTCCAGCCTGGG | 11124 |
rs189673696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50663028 | TAAAAGGTCAAACCT[A/G]GATTTTACGATAAAA | 11124 |
rs189677481 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50728774 | CTAGCCTGGGCGACA[A/G]AGCCAGACTCCGTCT | 11124 |
rs189685402 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50766316 | TTTTAAACATTATAA[A/G]CCATTACCCCCTAGA | 11124 |
rs189688720 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50645004 | AATAGAATTCATTTC[A/C]CAACTTTTCTTTTCT | 11124 |
rs189694395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736375 | CTAGTACAAAGCAAG[C/T]TTATCTGTCTACCAT | 11124 |
rs189695525 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701633 | ACATACAAAATCCGA[C/T]GTTAGGTTCAAATGC | 11124 |
rs189699552 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50684950 | ATTATACAAATGAAT[A/G]TTGTATGAGGCACAA | 11124 |
rs189704290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50477529 | CTTTTTTCTGATAGC[A/C]TGAGTAGCAGTTTAC | 11124 |
rs189710588 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50721998 | GCATGAAGAAGTCAC[A/G]CTCACAGAAAAATCA | 11124 |
rs189720759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742465 | CTCAGCTCACTGCAA[C/T]CTCCACCTCCCAGGT | 11124 |
rs189722285 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50772327 | AGAATTACCGTCCTA[C/T]CCCACAATCCCATTA | 11124 |
rs189729190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50549564 | GTGGGCGGACCACGA[A/G]GTCAGTTCAAGACCA | 11124 |
rs189736881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50523141 | CCATTGTATGGATAT[A/G]CCATATTTTTATCCA | 11124 |
rs189737109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50456503 | GTGGCCTCTCACTTG[C/T]CTGTCCTCAAGCTAT | 11124 |
rs189738989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815151 | CATGGCTATATTGCA[C/T]GATGCTGAGGTTTGG | 11124 |
rs189740650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50500202 | CTACAATAGCCAAAA[G/T]AATTATGGATAAAAA | 11124 |
rs189755591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948318 | TTATACAGAAAAGAG[A/G]TTTGTTGGCTCATGG | 11124 |
rs189761336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50572201 | CCTATTTATTCTTCA[C/T]CTAGATTTACCAATC | 11124 |
rs189769343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50950117 | AGTGCTGGGAATACA[C/G]GTGGGAGCCACCACA | 11124 |
rs189775334 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50915815 | AACTGTTGGACTGAA[A/G]ATAAGGCTAAGTCAG | 11124 |
rs189780121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50883815 | ATTAATTTACTGAGA[C/T]GTACAGTATTGAGTA | 11124 |
rs189786114 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50838780 | TAACTATAAAGAACA[C/T]ATCACTATTACTATC | 11124 |
rs189794428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50867696 | TAGCTGTTGCTGTGG[A/G]TGTGGTGAAAATAGA | 11124 |
rs189800949 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846603 | ACCTGGGTGAGTGAG[C/T]GCTTCCTTGTAAGAT | 11124 |
rs189801996 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50883209 | TCTGAACATCAAAAA[G/T]AAAAATGTCTGAAAT | 11124 |
rs189827024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50882917 | CTTGAACACGGGAGG[C/T]GGGTTGTAGTAAGCC | 11124 |
rs189829623 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50851318 | AACTAAGTGACCCAC[A/T]CGCATTGGCTTCCCA | 11124 |
rs189841100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50845785 | GAAATAAACCTCAAA[C/T]GAAACCTAACTCAAA | 11124 |
rs189845450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495256 | CCACCTTCCCCCACA[A/C]CCCACTGCCCTCCCT | 11124 |
rs189851220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50527732 | CTTATCACTCTTCCA[C/T]TGACCACCCCATTAC | 11124 |
rs189853640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565156 | GAAATATAACACCTT[C/T]TAAATTTGTAATATG | 11124 |
rs189863526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50507477 | GGTACAGTGGCTCAT[A/G]CCTGTAATCCCAGTG | 11124 |
rs189867527 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50450750 | GGGCATATGCTGAGT[C/T]AGGGTATAAAAAAAT | 11124 |
rs189872652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486943 | TCTAGTTACTATAAA[G/T]TCCATCCCTTAATCA | 11124 |
rs189873242 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50618393 | GTTGTTTAATATCCA[C/T]CTGTTTGTGTAGTTT | 11124 |
rs189879225 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50769414 | ATTCCAAATGCTTGA[A/G]GAAGAGAGACTCCTC | 11124 |
rs189887083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50793135 | TAAATCCTGACTTCA[A/G]TGACCACTGTGGAGA | 11124 |
rs189890061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576041 | AGAAATGTTCATGGG[G/T]TTCTCAAAATTCCTT | 11124 |
rs189893713 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50579016 | TCAGTGGATTTTGGT[G/T]ACAAATCTAATAGGA | 11124 |
rs189894665 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50605915 | GTCAGGCACTTGGAT[C/T]CAAATAACCTGGCCT | 11124 |
rs189897894 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50811981 | GGACTCCCTGTTCAA[C/T]AAATGGTGTTGGGGT | 11124 |
rs189898311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50558110 | CACTATGTTGGCCAG[A/G]CTGGTCTTGAACTCC | 11124 |
rs189900704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50532003 | TATTTCTAATTTTTT[A/T]AAAATAAAGGCAAAT | 11124 |
rs189907221 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50647395 | CTTTCTGTACGTCAC[C/T]TTCCTTTTTTTGTCT | 11124 |
rs189908488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50829117 | AAAAAGGCTGACAGG[C/T]AGTGAGTGGCAAGAA | 11124 |
rs189914419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50686960 | CAGCTTCCTGAGTAG[C/T]CAGGATTACAGGCGC | 11124 |
rs189927835 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687472 | TGCTCAAAACTGGCC[A/G]GGTGCGATGGCTCAT | 11124 |
rs189953530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50716227 | GTAGGCAAACTGTCT[C/T]GAACCAATAATAATC | 11124 |
rs189954803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451375 | CTAAGTGCTGTATAA[A/G]CACTCATACAACTCT | 11124 |
rs189957147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725487 | TTGAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGA | 11124 |
rs189957791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50755100 | ATCATGCCTTCCCAA[C/T]AGTCCCCCAAAGTCT | 11124 |
rs189972016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50763003 | GCTCATACCTGTAAT[C/T]CCAGCACTTTGGGAG | 11124 |
rs189977547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50795585 | TATGTGGTATAAATG[C/T]TTTATATCAGTGTCC | 11124 |
rs189979004 | snp | C/G | 0.030278 | 0.119257 | intron-variant | FAF1 | GRCh38.p7 | 1:50722534 | GGCGCCTGTAGTCCC[C/G]GCTACTCGGGAGGCT | 11124 |
rs189985388 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50743474 | CTTGGATTACAGGGG[C/T]GTGCCACCACGCCCA | 11124 |
rs189990905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50806693 | TTCCTAACCTCAAGA[A/G]TCCAGACAAGAATGC | 11124 |
rs189998025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50831244 | CACTCCGTGATCCAG[A/C]AGCACTTAAGAACCT | 11124 |
rs190001506 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50760103 | TGAGTAGGTTGCATA[C/T]TGGTAAAGGGATCAA | 11124 |
rs190005954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778842 | CAAAACACACAGACA[C/T]ACACACACACACACA | 11124 |
rs190018017 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50803995 | ATCTATGCTTCAAAC[A/T]ATGGGAAGATACAGA | 11124 |
rs190021408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833543 | TTCATTACATAGGCA[C/T]AATTGATTATCATTA | 11124 |
rs190026113 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50820541 | CTCTTAGCAAATTTC[A/G]AGACGTAAACAATAT | 11124 |
rs190048943 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50635560 | CCTCCTGAGTAGCTG[C/T]GACCACGGGTGCATG | 11124 |
rs190060547 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50614918 | CATGATTTATTTTTA[G/T]TTTTTAAATTTCAAC | 11124 |
rs190061743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897710 | ACCTTCCATGCATCC[A/G]TACCATTCAACTCTA | 11124 |
rs190062210 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | FAF1 | GRCh38.p7 | 1:50952802 | CTGCCCGGCCGCCCC[A/G]TCTGGGAAGCGAGGA | 11124 |
rs190064070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50920405 | ACAGCCCCAAGTACT[A/G]CTGCAGATGACAGAC | 11124 |
rs190066294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893801 | TCCCCCTAGGCCTTA[C/G]GGCAGGTCCAGGGAT | 11124 |
rs190077034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674920 | TTGAGATGCAGTTTC[A/G]CTCTTTGTTGCCCAG | 11124 |
rs190080304 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50860514 | TGTTCCACATCACCA[A/T]TCACAGAGAAATGCA | 11124 |
rs190086276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50866266 | CTGAAAGCATTCCCC[C/G]TGAGAACTGGAACAA | 11124 |
rs190094531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50691986 | TTTGGGAGGCCCAGG[C/T]GGGCAGATCACTTGA | 11124 |
rs190095370 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50552308 | TTTCCAAAAAAAAAA[A/C]AAAAAACTTCAGCTA | 11124 |
rs190100205 | snp | C/T | 0.000168645 | 0.00918119 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475659 | AGGAGGCAGGGCTTG[C/T]TCTAAGGACAGCCGG | 11124 |
rs190112912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50504298 | GAGAATACAGTGGAT[C/T]AAGCAATACCTAAAG | 11124 |
rs190123525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50597216 | AGATAAAATGTCCAG[C/T]GAAAAGGATGGACTC | 11124 |
rs190143121 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961980 | ATGAAAATAGGCTGG[C/G]CTACAGTTCTTAAGT | 11124 |
rs190144337 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561852 | GGACGGATGGACGGA[A/T]GGAAGGAAGGAAGGA | 11124 |
rs190149550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925138 | GTCTCTTCAATAAAT[C/G]GTGCTAAGAAAAATG | 11124 |
rs190153586 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50944646 | CAGAGACTCAGCAAG[A/C]AGTATACTCAACCAA | 11124 |
rs190162259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884986 | GGTTTTAGATTTCTT[C/T]ATGGTTGAATCTTGG | 11124 |
rs190163445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638173 | GCCCATGACCTTGCT[A/T]ATTTCACTTGTCACA | 11124 |
rs190166268 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50868733 | ACATCTTTTTGCTGT[G/T]GATTTGTAATTTAAT | 11124 |
rs190169852 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50907678 | TCATAGAGTTGTTTA[C/T]AGTATTCTCTGATGG | 11124 |
rs190172065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890236 | TTCCTCCATCCCTTT[A/G]TTTTGACCCTATGTG | 11124 |
rs190174938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50643790 | TAGAGCTGGGGTTTC[A/G]CCATGTTGGCCAGGC | 11124 |
rs190176883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50602146 | AGTAACACAAGTGAA[C/T]GAGATTCAAACTACA | 11124 |
rs190178304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50847286 | AAAAAAACAGACTGA[A/G]ATAGGACACAGATGT | 11124 |
rs190189651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50668438 | ATCAGCTTTCAGCAT[C/T]ACTCTCAGAGATTTG | 11124 |
rs190195304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50678323 | CTGGGTGGAGCAGGT[A/G]AGGGCCTAAAGTCTA | 11124 |
rs190195706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50705487 | TGTCAACAATTTCCA[C/T]AGTATTTTGAATAAT | 11124 |
rs190199558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50715247 | ATGCAAAATGCTAGA[C/G]ATTTTCAAACATATC | 11124 |
rs190208376 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50746156 | TAACTGGAGGAAGAA[A/T]TTTCTAAGGAACAAA | 11124 |
rs190228752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50780700 | ATGTGCTGCCACCTA[A/T]CATCACAGAAATCCT | 11124 |
rs190230930 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50747722 | GGTTTGGATTTGCAT[A/C]CCCAATCATGTTAAA | 11124 |
rs190231155 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50697837 | CATTGAGGGTAATAA[A/G]GTACTATACTATAGC | 11124 |
rs190235911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726510 | GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGG | 11124 |
rs190241661 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50763667 | ATTGCTATGTCTTCA[A/T]ATTCACTGACCTTTT | 11124 |
rs190247930 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50718258 | CTGGACTCAACTCCT[A/G]ACCTTGTGATCCGCC | 11124 |
rs190256431 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50782767 | AAGAAATATATTTTT[A/T]AATAAATTTAGGGTA | 11124 |
rs190260768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50781171 | TCTACCCTGCCTGCA[C/T]CTCTTTGGCCAACTA | 11124 |
rs190264824 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50807231 | TCCAACAATTTTAAA[A/G]CACGGTCACAGGTGT | 11124 |
rs190270024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50543947 | CGAAAGGTCAAGGGG[A/G]AAGTGGATCCATGTG | 11124 |
rs190273048 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50824362 | CCTATTTGAAGATAG[A/T]TATTATACTGATCAT | 11124 |
rs190273847 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50577295 | TCTGGGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 11124 |
rs190277463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823964 | TATACTTAGATTTTT[A/G]AAAAATGCTTTATTT | 11124 |
rs190278304 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519378 | GGAAGGAAGGAGGGA[A/G]GGAGGGAGGGAGGGA | 11124 |
rs190280413 | snp | A/T | 0.000106809 | 0.00730706 | intron-variant | FAF1 | GRCh38.p7 | 1:50452165 | GAACGAGAACAGGCA[A/T]GTTTCCCCATCCTGG | 11124 |
rs190290170 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50473344 | AATAAAGTTTAATTT[A/T]AAAATGCAAAGTCCT | 11124 |
rs190290339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50496276 | TCTACCAATAGGTCC[C/T]TGTCATCAGAGACAT | 11124 |
rs190305107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938408 | CATCAAAAGATGGCT[C/T]TGTATCCATTATTAA | 11124 |
rs190305647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50939110 | TGTTAAAAATAATCT[C/T]GGTAGTTTGATAGGA | 11124 |
rs190318036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50567421 | TTACTTTCTTACACT[A/T]TAAAAAGGCTGGGAT | 11124 |
rs190319089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50879551 | ATGGGAAAGATTCAG[A/G]GGCAGAAAACATTTA | 11124 |
rs190322549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904678 | TTGGGCATTTACCAT[C/T]TCAAGGGTAGAAATC | 11124 |
rs190327118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902763 | TAATACCTAATACAA[C/T]GTAAATGATATGTAA | 11124 |
rs190335179 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50870601 | TGTTTCAAACTTTTT[C/T]ACTATTATTATATAT | 11124 |
rs190338807 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50842300 | AGGTAGATACCAAGA[A/C]AAAGAGTCAAGGGTC | 11124 |
rs190341113 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50498309 | AACCATAACATTCTT[A/G]GATAAAAACATAGGT | 11124 |
rs190353600 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464991 | CAATCTTCCCCTGCC[C/T]GGTGGTATTTCTATC | 11124 |
rs190365891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454993 | TCCTCCCTAGAGCCT[C/T]CATGAATTCAAAGAA | 11124 |
rs190384461 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50506700 | TGCTTGGTAGTGAAT[C/G]CTTACTATACATACC | 11124 |
rs190385710 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50954786 | GACCTCAAGTGATCC[A/G]CCTGCCTCGGCCTCC | 11124 |
rs190386767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50548102 | AATTTATGTTTAATG[C/G]CATATAACATTTCTT | 11124 |
rs190390757 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50486421 | TGACTACTCTTGCAC[C/T]TCCCTTTGGTGTCCA | 11124 |
rs190392530 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50441927 | TTTGGGGCTGATCTT[A/C]CTCTTAGAACTACAT | 11124 |
rs190397578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582272 | CAGTGCTTCACAAGG[A/C]CTTCTGCAAGAGCCA | 11124 |
rs190406292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940300 | TATCTATCCAGTCAG[C/T]ATTGGCAGAGTATTT | 11124 |
rs190411496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50537131 | AGTCTCTGGGTTTCT[A/G]TGTTTTATTTAAAAA | 11124 |
rs190412585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922733 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCCAGGAG | 11124 |
rs190412965 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50623866 | GAGCCCAGGAGCCAG[A/G]AGGCAAGGCTGCAGT | 11124 |
rs190415196 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50905239 | TTTTATGGCTGCATA[A/G]TATCCCATGGTGTAC | 11124 |
rs190421196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50887503 | TCTAGGGTTTTTATG[C/G]TTTTAGGTCTAATAA | 11124 |
rs190422040 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661838 | CGTTCTGAACACATA[A/C]TTCATACCTAAGGCC | 11124 |
rs190426666 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622377 | TTCCCAGCTTCCTCC[C/T]TTTTCAGCCTTGGCT | 11124 |
rs190431938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50591454 | GTGGCAGGTGGATCA[C/T]GACTTAAGGTCAGGA | 11124 |
rs190454505 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50634229 | CAGTTGTAAGCACCC[C/T]TCTATTTTTGCACAT | 11124 |
rs190456156 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50695112 | TAACTTTCCTAAATA[A/C]TTTAAAGATTGTTGG | 11124 |
rs190472572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50734923 | TAGATATCAGGGAGA[A/G]GGTACAATAAGAAAG | 11124 |
rs190505931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948853 | ACAATCAGATCTCAC[A/G]TGAACTAACTGAGCA | 11124 |
rs190514208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50929749 | GGCTCCTGCCCCCAC[A/G]ATTCACAATTATTCA | 11124 |
rs190515152 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50806920 | TTCAAAGATTGAAGG[A/T]ATATCACCCACAATG | 11124 |
rs190518922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810496 | ATGGGCAAAAGATGG[A/G]AGCATTCCCCTTGAA | 11124 |
rs190528924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50778009 | CATGTACAAGAATGT[C/T]CACAGCAGCTTGGTA | 11124 |
rs190553639 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50922003 | GAAACCCCGTCTCCA[C/T]TAAAAACACAAAATT | 11124 |
rs190562217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944303 | TTTAATGTGATAACA[A/G]CAATTTGGAGGAGCT | 11124 |
rs190571602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50947322 | GAAAAACTAGGTGAC[C/T]CAAACCCCACCTGAA | 11124 |
rs190573001 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50589234 | GCTGTTTTCAGGCAC[A/T]CATGCAGTAGCTGTG | 11124 |
rs190577130 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50567690 | TCTGAACAATGGATA[C/G]TCTCTTCCATTTGAA | 11124 |
rs190578297 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50886612 | CAATTCCCACCTATG[A/C]GTGAGAACATGTGGT | 11124 |
rs190587650 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50880600 | GAGAAGGCAGCCATC[G/T]GCAAGCCAGGAGGAG | 11124 |
rs190593333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50649238 | TCTCACTGCAACCTC[C/T]GCCTTCCGGGTTCAA | 11124 |
rs190594544 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50848836 | GCTGAAGAATCAGCA[C/T]AAGTTGGGAGAGGCT | 11124 |
rs190600319 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468604 | AGCTGGGATTACAGG[C/T]GCCTGCCACCGCGCC | 11124 |
rs190600615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50696061 | AAACAATTCAAATTA[C/T]ATAAGTCAAATAGGA | 11124 |
rs190604593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608907 | ACCTCTGTAAAGTCT[C/T]ATAAGTTACAAGATT | 11124 |
rs190610675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50629840 | GAGACAGGCAGATCA[C/T]CTGAAGTCAGGAGTT | 11124 |
rs190612618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50679285 | CCTATGGAGTAACCA[C/T]TCTTTATTCCTTTAC | 11124 |
rs190619247 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50476338 | GTTTATTGGCAGAAG[A/G]AGACCACAGTCCTAG | 11124 |
rs190620440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50670931 | TAAGACTGCCTCAAA[C/T]ACATAAATAAATAAA | 11124 |
rs190620719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50716968 | AGCTGTAACACTTGC[C/T]GCAAAGGTCCGTGGC | 11124 |
rs190623243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50444039 | CTCTGGTGCCCTAAA[A/G]ATAAAATCAAGCAAT | 11124 |
rs190626210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50511468 | TGTTCTCATTGTTCA[A/G]CTCCCACTTATGAGT | 11124 |
rs190632000 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50755433 | CTTGGGCAGCTCCGC[C/T]CTTGTGGCTTTGCAG | 11124 |
rs190633789 | snp | A/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50736496 | GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA | 11124 |
rs190634503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50490253 | TCAACCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 11124 |
rs190639625 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50447414 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTATTC | 11124 |
rs190642592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50446708 | ACATTTAATATTTCT[A/G]AGGTAATGCTTTTAT | 11124 |
rs190646307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773114 | ATAACACCTACAATT[A/T]AAAAAGGATTATAAA | 11124 |
rs190650520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50522076 | TTTAAAAGTGAGCAT[C/T]ATTCCATGCACAAAA | 11124 |
rs190656055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50796711 | AACCACCCATACCTG[C/G]ACTTGGTGGTCCAGC | 11124 |
rs190660295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815588 | CATTGCTGGGTAGAA[C/T]GGCAGTTCTTTTTAA | 11124 |
rs190662129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50492142 | ATATACAAACTATCT[A/G]GCAAAGGACCTGGCA | 11124 |
rs190664805 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50642877 | ACAGAGTCTCATTCT[A/G]TTGCCCAGGTTAGAG | 11124 |
rs190672538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50612997 | GATCTTATATTCTCA[C/T]TTTTAGCTGCCATGG | 11124 |
rs190682684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50570888 | AACTGGATTAAGCAT[A/G]TCAACCAATTTGGAA | 11124 |
rs190689738 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50905061 | CCCACAACAGGCCCC[A/C/G]GTGTGTGATGTTCCC | 11124 |
rs190689998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50539262 | CAATTAATCAACATT[A/G]TAACAATAAATCAAT | 11124 |
rs190693572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50887027 | CTATTTCTCCAAATC[C/G]TCTCCAGCACCTGCA | 11124 |
rs190699088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621548 | GGGACTACAGGGGCG[C/T]ACCACCACACAGTTA | 11124 |
rs190706992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871280 | GCTGATGTAGAAGCT[A/G]TAGTAAGTTTTATTC | 11124 |
rs190709689 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50629022 | ATAGGGTTGCTGGGA[A/T]GGTTAAATGAGTTAT | 11124 |
rs190712841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849262 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 11124 |
rs190715443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669683 | CAAAATAAAGGATAA[C/G]TAATTGTGTATGTAA | 11124 |
rs190719588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50648252 | GACAAGAGTGAAACT[C/T]CGTCTCAAAACAAAA | 11124 |
rs190733205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50584299 | CCAAAGATGGGTACC[C/G]TTGAATAGAAAAGTA | 11124 |
rs190733745 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50687621 | CAGGCATGGGGCGCG[C/T]GCCTGTAATCCCAGC | 11124 |
rs190746259 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447336 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 11124 |
rs190755596 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50788907 | CACAATCTTGGCTCA[C/T]TGCAGCCTCAAACTC | 11124 |
rs190777766 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50827439 | AAGGCAGCATGCTCC[C/T]TAAGAGTCATCACCA | 11124 |
rs190787793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928831 | GCCAGGCACAGTGGC[A/G]CATGCCTGTAATCCC | 11124 |
rs190789511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948642 | GATTCAAGCGATTCT[C/T]ACGCCTCAGCCTCCC | 11124 |
rs190790496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50759830 | TGTTTCCTGACTTTT[C/T]AATGATCGTCATTCT | 11124 |
rs190798389 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960519 | CGGGGACCAGATTGT[A/G]CACCTCACGTGGTTA | 11124 |
rs190804950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912216 | AGAAAGCACAGGAGA[A/C]AGGAATGGTGTATTA | 11124 |
rs190805981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50802742 | TTCCAACTCTGTCTT[C/T]ATACCATAACAACTT | 11124 |
rs190808896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895271 | AAAACTTAGACCAAA[C/T]GTGGCAATTTCTAAA | 11124 |
rs190816389 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50925629 | GCAGAGAAAAGGGAA[C/G]TCATACACTGTTGGT | 11124 |
rs190816790 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50573405 | TGCCTGGCCTGAAGC[G/T]GAATTTTAAATATAC | 11124 |
rs190821463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881156 | CAAGAATTATTTTGC[G/T]AAAACTTAAAAGTGA | 11124 |
rs190825463 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50862870 | TACATACACTAAACA[C/T]TGGAGCTCCCATTTA | 11124 |
rs190826544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50891023 | AGATTTGGTCTTTTC[A/G]CATAGTCCCATATTT | 11124 |
rs190834441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50924841 | TACAAAAATTAGCTG[A/G]GTGTGGTGTTGGGCA | 11124 |
rs190834955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550042 | AAACAACTATCACCC[G/T]AATGGATATAAAAAT | 11124 |
rs190835713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50843352 | ATAAAATCTGGGTAA[C/T]TGGGATAACCATCAC | 11124 |
rs190846497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855864 | TTTTTGCTTGGGCCT[A/G]ATACAGTGTATGATT | 11124 |
rs190894679 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50472908 | TTCAGAGAAGAATGA[A/C]GGGCCTTTAACTCTC | 11124 |
rs190897946 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469331 | CCCATCTGCTGAATG[A/T]TATTAACACCACACC | 11124 |
rs190901497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50490969 | TGGTCTTCCTTTCTG[A/C]CCTTTTCTATCTACC | 11124 |
rs190902914 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50443114 | TCTGCCCACCTGCTT[A/C]TGATATTGTTCTTAA | 11124 |
rs190926573 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50562106 | AGAAGTGATACCTGT[C/T]CTGAATTTTAAGAAA | 11124 |
rs190930621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50797314 | TGAAAACCACCATCT[C/T]ATAATCTGACCTTGC | 11124 |
rs190932404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50537751 | ACCGTATTCTGTATT[C/T]TCGTACCTACATCTA | 11124 |
rs190935009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50591790 | CTTTTCCCCCGACTT[C/T]CTTCTGCACTAACAG | 11124 |
rs190935357 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50512046 | TAAAAGTCTTCTTTT[C/G]AGAAGTGTCTGTTCA | 11124 |
rs190936778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562571 | TTCTAACTTCATCTT[A/T]ATGTGTATCATCTCT | 11124 |
rs190942570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50816114 | ATTTCTCTGAATATT[A/G]GTGATTTTTTTTTCA | 11124 |
rs190945673 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50516552 | CAGTGGTTAAAGAGA[C/T]AGCACATGAATGGGT | 11124 |
rs190947947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834255 | TGTTTCCTGTACGGC[A/C]TGCAGAACTGTAAGC | 11124 |
rs190950619 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624631 | GCTTCAACATATGAA[A/G]AGGAAAACAAAAAAG | 11124 |
rs190955514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50607232 | GCCATAAGTCAGCCT[A/G]TGGTATGATTCCAGG | 11124 |
rs190957011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512953 | TGCTTAGTCTGCCTT[C/T]AGGTAATCACACTCT | 11124 |
rs190961735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50602460 | AATAAGGCAGTATTC[A/G]GTGCTATTAATATAT | 11124 |
rs190963610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602931 | ACAAAGTGCTTTACA[C/T]GCACTACCCCACTTA | 11124 |
rs190973721 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50566686 | TTGTGCAGAAAGTCC[C/T]GCCTTCTTCACTGAA | 11124 |
rs190976463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50635091 | ACTTTAAGTAACTGT[A/G]AGCACCAAAATAGAG | 11124 |
rs190984376 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50644461 | ATGCATGCACAGAGA[C/T]TGGTATTCAGCTAAA | 11124 |
rs191007283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50645651 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11124 |
rs191021914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50710892 | TAGGCATGAGCCACC[A/G]AGCCCGGCCAAGTGG | 11124 |
rs191033897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945070 | GAAGAAGCTGTTCCA[A/C]TATTCAATGTTTATC | 11124 |
rs191036715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685553 | CTTACTTATCTTCTG[C/T]ATCAGTATCTCTGTT | 11124 |
rs191037837 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50951157 | GAGAACTGCCTGAAC[C/T]GGGGAGATGGAGGTT | 11124 |
rs191042230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925957 | AGTGTGCCTCATGCA[C/T]GTAATCCCAGTGATT | 11124 |
rs191044208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909239 | GAGTTTCTGCCCAGA[A/G]ATCCGCTGTTAGTCT | 11124 |
rs191047635 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50944923 | TGATCATTACTCAGG[A/G]GTGATCAAGACGAGA | 11124 |
rs191050160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50891602 | TCAGCTGCAGGTCTG[C/T]TGGTGTTTGCTGGAG | 11124 |
rs191051927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778332 | ATCTGGATCTGGGTG[A/G]TGGTGGTTCCAAGGG | 11124 |
rs191053924 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50751612 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 11124 |
rs191059312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50752684 | TTTGCTCATTTTTTT[G/T]GTTTTGTTTTGTTTT | 11124 |
rs191060155 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50936148 | TTTAATATTCAGTGA[C/G]AACGTACTATGTGCC | 11124 |
rs191061167 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50876639 | CACCCAGGCTGGAGT[A/G]CAGTGGCGCAATCTC | 11124 |
rs191066055 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50820200 | TGCAAGATGAAAAAG[A/T]TCTGGAGATTTTTTT | 11124 |
rs191067751 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50790629 | AGAGAAGGTGGTGGG[A/G]AGAGAGAGAACCATA | 11124 |
rs191070337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908184 | TAGTTGAGTGGTTTC[A/G]AGTGAGCTTCTTAAT | 11124 |
rs191081484 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50828292 | TTCTTTTTTTGAGAC[A/G]GAGTCTCAGTCTGTC | 11124 |
rs191083458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50900740 | TTTCCAATATAAATC[A/G]TCATTTTTTATAAAT | 11124 |
rs191087146 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875889 | TTTGATAAAACCAGT[C/T]ATTCAAATCCTCCTT | 11124 |
rs191114259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875303 | GAATATATTTATCAC[A/G]TACAATATAATGTTT | 11124 |
rs191133684 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676188 | GAGGCCAGCAGATCA[C/T]CTCAGGTCAGGAGTT | 11124 |
rs191135981 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50838065 | CCTTTATACAATGTG[A/T]CCCTTAAAAACATAA | 11124 |
rs191148557 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FAF1 | GRCh38.p7 | 1:50953182 | GCTTTGTTAAACAGA[C/T]GCTTGAAGGCAGCAT | 11124 |
rs191149647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50692570 | CACTTAGCATGCTGT[C/T]CTCCAGGTCTTCCCA | 11124 |
rs191151973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495935 | TCAGCATAGTCCTCT[A/G]TCTCCGAGACAATAG | 11124 |
rs191152608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463896 | AAAACTTCTTGGATG[C/T]TTGGTCACATTTCCA | 11124 |
rs191163914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50732871 | CCTTTCTTTCTTCTA[A/G]ATGTATGCAGGTTAT | 11124 |
rs191171179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50712632 | CTGCACTCCAGCCTG[A/G]GCAGCAGAGAGAGAC | 11124 |
rs191182053 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50752062 | GCAACCTCCGCCTCC[C/T]AGGTTCAAGCGATTC | 11124 |
rs191184720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768601 | ACTACTGAACCAGTG[A/C]AATAAAAATAGAAAT | 11124 |
rs191187225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50502582 | TGACTCACAAGTATA[A/G]ATTGTATAACCATAT | 11124 |
rs191187944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543570 | TTGTGCCTAAAATAT[A/G]GTAGGCCCTTAAAAT | 11124 |
rs191190985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505615 | TGGGCCAAAACTGAT[G/T]TGTGGCCTGTTTTTG | 11124 |
rs191195231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479916 | AAAAAATAACAAAAA[C/T]ACATCAGTAGTTCAG | 11124 |
rs191199955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50791487 | TAAAGAGGGGAGGAG[A/T]TTAGTAGAGATTAGT | 11124 |
rs191206350 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465456 | TGTTAATTTGCATCA[C/T]TCATTCATTCATTCA | 11124 |
rs191210836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50574123 | GGGGCGAGACTCTGT[C/G]TAAAAAAAGAAAAGC | 11124 |
rs191212530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50459088 | GTGTTCCTCCTGTTT[C/T]GGCCTCCTGAGTAGG | 11124 |
rs191216716 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50551227 | TAAATGGAAAAAAAA[A/C]CCAGACATATATACA | 11124 |
rs191223728 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50587875 | AGATGATAACTAAAC[C/T]GTTTAAGGTAAACAT | 11124 |
rs191230978 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50525494 | TCATGTAAGATCATG[C/T]CATCTGCAAATAGAG | 11124 |
rs191232656 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50553961 | AATATTCAAGCACAG[G/T]CTGGAGCAACATCAG | 11124 |
rs191237203 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50615973 | CGTTTTCTTCTGGGA[G/T]TTTTATAGTTTGAGG | 11124 |
rs191238103 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50827164 | AATGGGCCATGATGA[C/T]GATGGCGGTTTTGTC | 11124 |
rs191239496 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50588173 | ACGCCTGTAATCCCA[A/G]CTACCTGGAAGGCTG | 11124 |
rs191245622 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50594731 | CAAAAATTAGCTGAG[C/T]GTGGTGGCGGGCACC | 11124 |
rs191259312 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50664913 | ACAAGACCTTGTCAC[A/G]AAGGGCAATATTTCC | 11124 |
rs191272134 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50670117 | CAAGAGCAAAACTCC[A/G]TCTCAAAAAGAAAAA | 11124 |
rs191275544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50730653 | CAGAAGCAGGGCTCC[A/G]CTACTCTTGACAGAG | 11124 |
rs191280179 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50629367 | AGAGACAGGGTTTCA[C/T]CATATTGGTCAGGCT | 11124 |
rs191296348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768129 | CAACAGAAAACAGAA[C/G]AAAACAGGGGTTGCT | 11124 |
rs191298772 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50702459 | ACAGACTATCACAGA[A/G]TTACTGTCACATTCT | 11124 |
rs191311814 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951979 | TTATGTGTCACTCAA[C/G/T]GTAAGTGACTTACCA | 11124 |
rs191313807 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917541 | CATTGAGTCAGATAA[C/T]TAAAAAGCTTAATTT | 11124 |
rs191315872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50811075 | CATGGTGGCTCATGG[C/T]TGTAATTCCAGCACT | 11124 |
rs191325837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50737624 | CATACGGTCTAAACA[C/T]AGAAAATAAAGAGCA | 11124 |
rs191346154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50774827 | CACCATTTTATAGGA[A/G]GACAAATGCTTTAAA | 11124 |
rs191363558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50911911 | GCATGGTGGCATGCC[C/T]CTGTAGTCCCAGCTA | 11124 |
rs191365442 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50816508 | CACGCCTGGCTTTTG[C/G/T]CCACTTTTTAACGGG | 11124 |
rs191368804 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50854922 | GCTCGATGGAACATT[A/T]TGGATGATGTTTGAA | 11124 |
rs191379686 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50849903 | GTGTACATTTATCAA[C/T]ACAGCTCTTCCTTAC | 11124 |
rs191382480 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | FAF1 | GRCh38.p7 | 1:50441370 | GTGTGGGTGGGTTGG[C/T]GAGGAGCCCTTCTCC | 11124 |
rs191391491 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50846943 | TTTTATATATAAGAG[G/T]GTATTGCAGGTGCTG | 11124 |
rs191411805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50646778 | TCATTGCAACTTTAA[C/G]GGCCAGCACAGTTAC | 11124 |
rs191415743 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50952287 | TGGTTTTCGTATCTT[G/T]TTGGTGGAGACGGGT | 11124 |
rs191427360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528742 | TACAGAGTGTGCCTG[C/T]CTCTTCTGCCTCCTC | 11124 |
rs191430741 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936627 | TATGTAAGCAATTTA[A/G]TATGAAATTCAAAGG | 11124 |
rs191434840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667248 | AGGCTCTTCCTCTTA[C/T]ACACTTTTGGCCAAT | 11124 |
rs191440604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50485805 | GCCTCAAGAAATTTA[C/T]AATCATGGTGGAAGG | 11124 |
rs191443012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50704819 | GTTATTCATGTCAAA[C/T]TCAGAAGCTGAAATT | 11124 |
rs191447560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50901474 | GCCAAGGTGGGAAGA[C/T]TGCTTGAGCCCAGGA | 11124 |
rs191451195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50918154 | ACTTACAAAGAGTAC[A/G]TTTCACTGAATGTAA | 11124 |
rs191451335 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50686628 | GGGGAGGGGAGCGGG[A/G]GAGAGCGGAGGAACA | 11124 |
rs191455587 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50724598 | GATAAAATTTCTGCC[C/G]ATGATGATTCTCCCC | 11124 |
rs191455729 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50858657 | AGCTTAAATAAAACA[A/T]GTTAAAATTAATTTC | 11124 |
rs191463199 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50840827 | TCATTGTTTTACTTA[C/T]GGTAAAGAAAAATTA | 11124 |
rs191464957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50885307 | TCTTTCTCTCTCTCT[C/G]TCTCTCACACACACA | 11124 |
rs191469507 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869125 | CTCCCGCGATTATGT[A/T]TCTTTTATCTTTGGT | 11124 |
rs191471490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50761016 | GGGATATCACCACCG[A/T]TCACACAGAAATATA | 11124 |
rs191474420 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50453900 | TCAGAGAACAAGCAT[A/C]ATTTGGGGAACTGCA | 11124 |
rs191475201 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50745374 | CAATTTAAACTGTAT[G/T]AAAGAGAAGAGCAAC | 11124 |
rs191476123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607778 | TATCCAGTGACACTC[A/G]GACAAATCTTCCAGA | 11124 |
rs191493195 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50577792 | TCATAAAACTGATCA[C/G]TACATTATCAGAAGT | 11124 |
rs191496450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50648867 | GGAGGCGGAGGTTGC[A/G]GTGAGCCAAGATCGT | 11124 |
rs191500357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50530640 | ACTTAAAGAATGTAA[C/T]TGGATTGTTTGTAAC | 11124 |
rs191513252 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50616844 | CGCCACCATGCCCAG[C/T]TAATTTTTGTATTTT | 11124 |
rs191522623 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50575845 | CAACTACAGCTGTGG[C/G]CTCAAATTTGTATAG | 11124 |
rs191524341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50595945 | ACAGAGCGAGAAGGA[A/G]CACATTAGTAGTAAC | 11124 |
rs191525462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688744 | TTGAACCCGGGAGGC[A/G]GAGGTTGCGGTGAGC | 11124 |
rs191526911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619039 | TAGGATTACAGGTGT[G/T]AGCCAGCACACCTGG | 11124 |
rs191538921 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50920428 | TGACAGACATTGTCC[C/T]TGATTGCCTGGCTCA | 11124 |
rs191541059 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50926965 | ACACATGCTATAAAA[C/T]GGATGTAACTTAAAA | 11124 |
rs191542951 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50902792 | AAGTAGCTGTTATAC[G/T]GTATCTGTTTTTTAT | 11124 |
rs191544785 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50677486 | ATAAAAATGACTCAT[A/C/G]TATTTCTTTAGTAAT | 11124 |
rs191544975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638014 | TTTCAATGTATAGAT[A/C]TTATAAATATTTTAT | 11124 |
rs191547460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659031 | TATATTTAATAAAAA[A/G]TTGAAATCATAATCC | 11124 |
rs191548888 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50885997 | TTAACATCAGCCCCC[C/G]TCTTTTTAACTTTTT | 11124 |
rs191548922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945792 | GGCAAAGGTCCGTAG[A/G]AATACAACAAGTTTC | 11124 |
rs191553387 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50656248 | GAGGCAGGAGAATCG[C/T]TTGCATCCGGGAAGC | 11124 |
rs191560264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694364 | AGAAACAAATGCTAA[C/T]AGCATATTTTGAATT | 11124 |
rs191560497 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50869908 | GCATCTGCTGAATGT[A/G]ATTGTGGCTTCTCCT | 11124 |
rs191569227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848419 | GAAACCTAGGATAAC[A/T]ACTAAAAATAATTTT | 11124 |
rs191573498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714221 | ATTTGCATTATCTTC[A/G]CCTGGGTGTCGTGGC | 11124 |
rs191577953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689355 | TTTCAGAGGCCGAGG[C/T]GGGTGGATCACGAGG | 11124 |
rs191581972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756081 | CTTATGCAAATTTCT[A/G]CAGCTGGCTTAAATT | 11124 |
rs191588432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50727392 | GTAGGATGATACTCA[A/G]TATATATCTGGTCAA | 11124 |
rs191598798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50763950 | TCCCTCCCTTCACCA[A/G]CTATATAGCTGTTTG | 11124 |
rs191601101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50798379 | GTGGCTAAAATTATG[C/T]TATTAATTTATAAAG | 11124 |
rs191609608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928580 | CAAGGTCAAGAGTTC[A/G]AGACCAGCCTGGCCA | 11124 |
rs191612625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50872156 | ATGGATCTGGGCAAA[A/G]TACACTGAAAACTTT | 11124 |
rs191613288 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50895725 | ATCCCAGAGATGCAA[C/G]GGTGGTTCAATATAC | 11124 |
rs191615593 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50953972 | TTTTTTATTTGAGAC[C/G]GAGTCTCCCTCTGTC | 11124 |
rs191617186 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834647 | GAACAAAGCAAATAA[A/C]TATAAAAGTCACAAC | 11124 |
rs191619159 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50808087 | ACAAGCCAGAAGAGA[C/T]TGAGGGATTATATTC | 11124 |
rs191624973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894986 | AACTGGAAAAATAAA[C/T]GCAAACCAAGCCAAA | 11124 |
rs191629582 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50868283 | CACCACTAAAGTACT[G/T]ATCATTGTAATCAAA | 11124 |
rs191633085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922675 | AATACAAAATTATCC[A/G]GGTGTGTTGGTGCAT | 11124 |
rs191638109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863266 | GCTCCTGAATGATCT[C/T]TGGGTCAACAATGAA | 11124 |
rs191704920 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50745756 | ATTATCCAGTCTCGG[G/T]TATTTTTTATAGCAG | 11124 |
rs191714897 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50762878 | TCTGCACAGCAAAAG[A/T]TACTACCATCAGAGT | 11124 |
rs191728979 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50780100 | ACAGTAAGTCCTTTC[A/C]TATCAGTAATTGCTT | 11124 |
rs191735710 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50806601 | ACCCGCTGAGACAAA[C/G]GGCATTGGCTAGCAC | 11124 |
rs191739959 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50523909 | TTGGGTAAATACCCA[C/G]TAATGGGATTGCTGA | 11124 |
rs191741163 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | FAF1 | GRCh38.p7 | 1:50822778 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 11124 |
rs191742513 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50498031 | ATAAAGCTACAGTAA[C/T]TGAAACCGTGGTAGT | 11124 |
rs191749444 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50474507 | GAGATTTTGGTGTAC[C/G]CATCACCCAGTGGGT | 11124 |
rs191755472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50556293 | ACAACCTGGATGAAA[C/G]TGGAGGTCATCATGT | 11124 |
rs191758668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454582 | TCAATCCATGTTTAC[C/T]GGACTAATACCTTTA | 11124 |
rs191759414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50478198 | AGATGGAGTTTCACT[C/G]TGTCGCCCAGGCTGG | 11124 |
rs191760902 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569722 | AAGAACACTGCAATG[G/T]AACATTTAGACTTTG | 11124 |
rs191763100 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50599852 | CCTTATTTAAAATGC[C/T]TGGGACCAGAGGTGT | 11124 |
rs191765220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621940 | GGAGGCCAAGGCAGG[A/C]GGATGGCCTGAGGTC | 11124 |
rs191768932 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50639484 | ACCTGATTGTATATG[C/T]TTTCTTAGTTTTGTT | 11124 |
rs191776259 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50545974 | GGAGTTGAAGACCAA[C/T]CTGGATAACAAAGTG | 11124 |
rs191776953 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50599128 | TTATTTATTTATTTT[C/T]TTGAGAGGGAACCTC | 11124 |
rs191784918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521076 | AAATTGTATATATCA[C/T]GTATAATCTGATGTT | 11124 |
rs191787214 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50660550 | CGCCCAGGCCAGAGT[A/G]CAGTAGGTTCTCGGC | 11124 |
rs191789613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50957846 | AACAAAGTTATAATT[A/G]CTTTATAAAGTTTTT | 11124 |
rs191800399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591091 | TTGCTGTGAGTTTTT[C/G]AGATATGTCTTTCAT | 11124 |
rs191800567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681248 | GACAGGGTTTAACCA[C/T]GTTGGCCAAGCTGGT | 11124 |
rs191803055 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50641774 | AAAGGAAAATGAAAT[A/C]TCTACCTGTGTGTCA | 11124 |
rs191806003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923826 | ATCAAGAACCAGAAT[C/T]ATATTTTCATTTAAA | 11124 |
rs191808014 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50943644 | AAAGATAATTCTTCA[C/T]AGGGTGTGCCTAAAT | 11124 |
rs191825776 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50906696 | GTCTGTTATTGGTGT[A/G]TAGGAATGCCTGTGA | 11124 |
rs191826262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50640655 | CTTTCAAGCAACTTG[C/T]CCATTTCAGCCTAGT | 11124 |
rs191829533 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50680287 | CTTAAATAAGGTACA[C/T]TTTATAGAAAGAATG | 11124 |
rs191838212 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50717871 | AATTGTATGTTTATT[C/G]TATATGAATTATAAC | 11124 |
rs191840840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50706747 | ATAAAGACCTATCAT[C/T]AGTATGCCTGAATAA | 11124 |
rs191849154 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50941037 | GGGTTTTTTTGGTTT[G/T]TTTTTTTTTTTTAAG | 11124 |
rs191859606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50755773 | TTCTTGACTTCTGTG[C/T]ACTTGCAGGCTCAAC | 11124 |
rs191882383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50794700 | GCAATCTTGCCTCAC[C/T]GCAACCTCTGCCTCC | 11124 |
rs191886455 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50813470 | TTCCTTTTAAAAAAA[A/T]TTTTTTTTGAGACAA | 11124 |
rs191891482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50747969 | GCCTCCCCAGAAGTA[A/G]ATGTTGCCATGCTTC | 11124 |
rs191898037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939851 | TCATTTTGAAGTAAA[C/T]TCTAGATATATCATT | 11124 |
rs191903717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912415 | AAAGTTTGAGAAGCA[C/T]GAGTATAGTGGAAAA | 11124 |
rs191907568 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50826702 | ATATTTAAAAGATCA[C/T]AAAAGAATATTATGA | 11124 |
rs191920263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749588 | CTCAGAAGTTTGAGA[C/G]CAACATGAGCAACAC | 11124 |
rs191924964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50863687 | GTTGTGTCTCTGCCC[A/G]GCTTTGCTATCAGGA | 11124 |
rs191925377 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50881842 | ATTCTTTAATAGCTG[A/C]AGAAAAAGTGCATTT | 11124 |
rs191925712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824714 | TGCCTATCAGTGGAT[A/G]AAGAGATTTAAAAAC | 11124 |
rs191934420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50844619 | ACAGCAGTGTCAACA[A/T]AATGATGGAGCCAAG | 11124 |
rs191938871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766046 | GCAGTGAGCCGAGAT[C/T]GCGCCATTGCACTCC | 11124 |
rs191940331 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50844151 | TTAGCATTTTTTCAT[G/T]TACCTGTTGACCATC | 11124 |
rs191941219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50787365 | AGGTGATTAGGCAAT[A/G]AGAGCTTTGTTAATG | 11124 |
rs191951801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808951 | TAACTATCCTAAATA[C/T]ATATGCACCAAACAC | 11124 |
rs191983313 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661408 | TTTGATATGGCAAAA[A/T]ACAAAAACAAAATGT | 11124 |
rs191989661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50501089 | GGTATTTATGAAAAA[C/G]AAAGTCATAGTGACA | 11124 |
rs191990850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469089 | CTTTTAAACCTTTTG[C/T]TATTTACTTTTTTTT | 11124 |
rs192000874 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50457136 | TCACATAAAGCCAAT[C/T]AGAGGAGGGAAAGTG | 11124 |
rs192015219 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50550329 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 11124 |
rs192027782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636126 | TCTCAGATCAACATA[A/C]TCATCCTAAATCCAC | 11124 |
rs192038910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50593923 | CAGTTTAAATAAAAA[C/T]GAGCAACCACATTTT | 11124 |
rs192044087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50663575 | ACCCGGCTAATTTTT[C/G]TATTTTTTTAGTAGA | 11124 |
rs192049001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50700361 | TCGAACGCAGCCCCC[A/G]GCCTTTGTAATTCTA | 11124 |
rs192050895 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50500326 | GACAGAAAAAAAATG[A/G]AAAAAAAATAAAGTC | 11124 |
rs192055903 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50741777 | CAGCAGTGGCTATAA[C/T]CATTGTGCTACTTCT | 11124 |
rs192057027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50487873 | TTCTGATCCAGATTA[A/G]GTGTTCAACCAGTTT | 11124 |
rs192091013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50443891 | CTTGTTTCTTCCCCA[A/C]GGCCCAGCAAGAGTG | 11124 |
rs192093299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50533916 | AGCTCCTACCAGCTA[C/T]ATGGCCTTGGGCAAA | 11124 |
rs192096657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50698136 | TTACCCATCCTTTGG[C/T]TTAATTTCTTGTGTG | 11124 |
rs192098338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467022 | CAGCAGGGATCTATT[G/T]CCCCTTTTGCTTGAC | 11124 |
rs192101688 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50509827 | TTTCTGTGCCCTTGG[G/T]CAAGTTCCTTGACCG | 11124 |
rs192102551 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50906342 | TGTTCTTTTGGCTTA[C/G]TATTGTCTTGGCAAT | 11124 |
rs192103452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50544751 | CAAAGCAGGGAAGGG[A/G]AGGTTGTAATATAAA | 11124 |
rs192105752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923197 | GCTGAGGTGGAAGGA[C/T]TGCTTAAGCCCAGGA | 11124 |
rs192108233 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50718874 | AAAAAGCGTGACACA[C/T]GGCAATTTAAATTTC | 11124 |
rs192110080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50811163 | AACATGGCATAACCC[C/T]GTCTCTATAAAAAAA | 11124 |
rs192114232 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50672832 | GTTATTTTAAAGTAG[C/T]CTGAGGCAGGGTGCA | 11124 |
rs192115925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916712 | ATGGAAGCCTTCATA[C/T]TACTTCTCCTAGAAG | 11124 |
rs192120394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888035 | TTCTTCCATTTGTTT[C/G]TATCCTCTTTTACTT | 11124 |
rs192120948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50950030 | TTTTTTTGTAGAGAC[A/G]CGATCTTGTTATGTT | 11124 |
rs192124033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884396 | AGCCGGGCATGGTGA[C/T]ATGCACCTGCAGTCC | 11124 |
rs192124619 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50873854 | TTTTCTGTGCAAAGC[A/C]AAGAAACCTCCCAGG | 11124 |
rs192130012 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50738508 | TGCAGAGCTCAATGA[A/G]TTTTCCTCAAAGGTA | 11124 |
rs192132571 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50690589 | CTGGGTGACAGAGCA[A/C]GACTGTCTCAAAAAC | 11124 |
rs192133521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659592 | TTTTGTCTTACACAT[C/T]TTTTTTTTGATCAGC | 11124 |
rs192134467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50851032 | TAAAAAATATCAGTA[C/T]ACAGTGCATCTGATT | 11124 |
rs192138876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756501 | TCTGTCTTCTTCATA[A/G]CCCTCCAAACTATTC | 11124 |
rs192144633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775446 | TTTTATGGGATCATA[A/G]CGGATGATTCAACTT | 11124 |
rs192148734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50696906 | ATCAAAATATATACT[C/T]AGCAAATTGTTTGGC | 11124 |
rs192149547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50799216 | AAAATAAGACAATCT[A/G]GACTTCACTACCTGC | 11124 |
rs192156396 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50955998 | TGAGGAGAGAGGGAT[A/G]TAAGGACTTATTGTT | 11124 |
rs192158326 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50818324 | CAGCTACTTTGGAAA[C/T]AGCATGGCAGTTTCA | 11124 |
rs192162232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923038 | AAATGGATAAATTTC[C/T]AGATACAGATAACTA | 11124 |
rs192162567 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50817109 | ATATTTTGAAGTCGG[C/G]TAATGTGATGCCTCC | 11124 |
rs192169022 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50774106 | CACAATTGATGGCAC[A/G]GAGGCAACAGACATC | 11124 |
rs192169432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50835919 | TGTGGTACACTGCAT[C/T]TAAAATAATCTGTGG | 11124 |
rs192255828 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50494326 | TTAACACTTCATGTA[A/T]AAATTTGTTCTCATA | 11124 |
rs192262575 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50446903 | TTAGGAAACAAGACC[C/T]AGAGACTGGATTTGT | 11124 |
rs192276441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50585975 | GGAGGATCACTTGAG[C/T]CCACGAGGTCAAGGT | 11124 |
rs192290105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541134 | AATTTTTAAAGCCAA[A/T]ACATTTTCTGTCTAT | 11124 |
rs192293891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50626664 | GGGGTCCGGTCTTTA[C/T]ATGGGAAGATTTAAG | 11124 |
rs192304831 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50693630 | TAAAAAATAAAATTT[A/C]TTATTATTCATTAAA | 11124 |
rs192314856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50654477 | TGAAATTTACTCTCA[C/T]AGAAAACAGCAATGA | 11124 |
rs192316873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927049 | CCACGTCTATAAGTA[C/T]TCAAACTCACAGAAG | 11124 |
rs192320740 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50524466 | GCTTTGCCCATGCCT[A/G]TGTCCTGAATGGTAT | 11124 |
rs192327849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50539936 | AGCAGGAAGCATACC[C/T]TAAATGCTGTCTGGG | 11124 |
rs192330584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892676 | GGTAGTCTTTCAGTT[C/G]AATCAGCTTGGTGTT | 11124 |
rs192333361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50448010 | TAGAAGTGTGAGGGC[A/G]AGTCAGTGGAGTAAA | 11124 |
rs192338428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513371 | TGCCTGCAATCCCAG[C/T]GATCAATACTTGAGA | 11124 |
rs192341449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469736 | TTTGGGCTATGACGA[C/T]TTGGGCAGTGGTATA | 11124 |
rs192343518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50733134 | AACATATATAACAGG[C/T]TTGCCAAAAAACCTG | 11124 |
rs192344650 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50492528 | TTAAAAGTTAATTCA[C/T]GAACAGAATTTCCCA | 11124 |
rs192358030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50573796 | GGGAGCACTGTCATA[C/T]GGAAGTCAGAGGGTT | 11124 |
rs192376133 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50580975 | AGATGGGGTTTCACC[A/T]GGTTGCTCAGGCTGA | 11124 |
rs192378778 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50601606 | AGAACTGTTTGAACC[C/T]GGGAGGCAGAGGTTG | 11124 |
rs192386088 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50805632 | AACAGTGGCATGTAA[A/T]ATAAATCATACCCTA | 11124 |
rs192387275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684544 | ACATACAACCAATGA[C/T]ATACCGGTAAATGGC | 11124 |
rs192392172 | snp | C/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50615415 | CTGTTGGGTTGAATG[C/G]TAGCTCTGATTTAAG | 11124 |
rs192394405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560821 | CACTAACCCACTTAT[C/T]ACTGGTTAATACTGG | 11124 |
rs192395847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50643181 | GTTTTATCTCTTTTA[A/G]TGGATTTTTAGCTAT | 11124 |
rs192395925 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50931483 | GAAAGGCACTTCTTA[A/C]ATGGTGGCAGTGAGA | 11124 |
rs192397885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671892 | AGTCACTGCAACCTC[A/T]AACTCCTGGATTCAT | 11124 |
rs192403702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949483 | TGCCCAATGTCCCCT[A/G]GGGGACAGAAATCAC | 11124 |
rs192414004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689769 | TAATGAATAAAATAC[A/G]GATTACATGTGGCAA | 11124 |
rs192414169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50622523 | GTTAGCTATCTCATC[C/T]ACTCTCTTGAGAGTT | 11124 |
rs192415693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50915054 | ATGCTTCTGTCCTCT[C/T]CTACTCTTCTTTTTC | 11124 |
rs192416931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50654271 | TTCAGTATTGATCAT[C/T]ACAAGATGTTTACAA | 11124 |
rs192419197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897681 | TGGACTGTGGTATTG[A/T]ACCCAATTCTTCAAC | 11124 |
rs192421215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50727646 | TCGGGTGTCAACTTG[A/G]TTGAAAGTATTGCTC | 11124 |
rs192422701 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50721435 | GGCCAGGATGATCTC[A/G]ATCTCACGACCTCAG | 11124 |
rs192423249 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50882787 | GGTCAGGAGTTCAAG[A/T]CCAGCGTGGCCAACA | 11124 |
rs192423535 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50707884 | CCATAGGAGTTAAGA[C/G]TTTGATTTTATTCAT | 11124 |
rs192426417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50758346 | GGCATAAGCCACCAC[A/G]CCCAGCACAACATAC | 11124 |
rs192436199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50865893 | TCACAGACCATTACC[A/G]AGATTAACCAAAAGA | 11124 |
rs192439822 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50748268 | TGGGAGGCCAAGGCA[A/G]GCAGATCAACTGAGG | 11124 |
rs192440221 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50817546 | TTTAAAAGATGAAAA[C/G]AGTTAGATGGGTGGT | 11124 |
rs192444062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50764906 | TAATTCAATTTTACA[C/T]GAAAATGTCTATCTT | 11124 |
rs192447680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50836469 | TAGGGACAAAAATTG[A/G]ACCAAAATAGTAAGT | 11124 |
rs192485051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50934123 | TCCTATTTATTAGTG[A/G]TTGTTCTCAGAATTA | 11124 |
rs192492719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50828645 | CTTCAGGCTCTCTTA[C/T]ACCAACACAAAATTA | 11124 |
rs192496943 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50900370 | ATTCTAATCTTTGGG[A/G]AAATTAAGGTGTTTT | 11124 |
rs192500791 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50520836 | AGCAACAGAGTGACA[A/C]CCTGTCTCAAAAAAC | 11124 |
rs192529468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50800050 | GTTTCATTCCTTCAA[A/G]AAAAGCAAACAAAAC | 11124 |
rs192535911 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50603286 | TCTGTAAATTAAAGA[C/T]TATCGTGATTGTACA | 11124 |
rs192540412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50478876 | TTTTAAAGTTTTTAT[C/T]AAAGTATAACATACA | 11124 |
rs192542105 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50527053 | GTAGAGACAGGGTTT[C/T]GCTATGTTGGCCAAG | 11124 |
rs192543632 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50563181 | AGTGATTTGCAAGAT[A/C]TTCTTGTTTACTATT | 11124 |
rs192548100 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50458542 | GCGGTAAGGGCAAAA[A/T]TTTTAAGGCTCTGAA | 11124 |
rs192552603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50837059 | GCATCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 11124 |
rs192560022 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50540637 | ACTGATAAAGCTTTT[C/T]TCTTCTATTAGAGGA | 11124 |
rs192564810 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938412 | AAAAGATGGCTCTGT[A/G]TCCATTATTAACTCA | 11124 |
rs192567218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50514772 | TTACTAATTTCTTTA[A/G]TGACAGAATTTCAAA | 11124 |
rs192578547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585636 | GTCCAAGCAAGATAT[C/G]TGGCTACATGCTTGT | 11124 |
rs192586489 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50563463 | ACCTTTAGCACTTCT[C/T]AAGACTACCAAGGGC | 11124 |
rs192596607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50910208 | AAGCAAATATTGCAG[A/G]ACGGCAAATGTTGCT | 11124 |
rs192600068 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50646446 | GTTTATTGCCATAGA[C/T]GTCAACTTTGTGGAG | 11124 |
rs192607794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50603932 | GCTCAAAAAACTGTG[C/T]TCTCTGCCTGGCCTT | 11124 |
rs192609521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626102 | CTTCAGTAGGAAGAA[A/T]CTATCTGCTTGGGTA | 11124 |
rs192623335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50877779 | CTGACTAACAGAAAC[A/G]GCTGTTGTGAAAGTT | 11124 |
rs192625143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753496 | CCTCCATTTCTCTTG[A/G]GAACCTATGTAGAAA | 11124 |
rs192625570 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50665815 | GGTTACAAAATAATA[C/T]GCATCTCTGTTTAAG | 11124 |
rs192633731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471163 | CTGCTTCTATCTCCT[C/T]ATGGTGGCAAATAGT | 11124 |
rs192640035 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50839637 | ACCTGTCAGGTCCTT[A/T]TAATACTTGTATCAA | 11124 |
rs192642285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50794208 | TTGAAAGCACATGAA[A/G]GTGAAAGCTGTACTT | 11124 |
rs192655555 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50694773 | CAACATGGTGAAACC[C/G]CATCTCTACTAAAAA | 11124 |
rs192657576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50515431 | TGTTATACAGGAAAT[C/T]TGTGAAAACACAGAC | 11124 |
rs192660719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50830236 | GATTCTGCTGCCTCA[C/G]CCTCCAGTGTAGCTG | 11124 |
rs192674512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50715054 | CATTATCAACAAGGA[C/T]ACAATTTGGTTTCTA | 11124 |
rs192683451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50564734 | TTTAGATGAATCTGT[C/G]ATATGATAGGTGGCA | 11124 |
rs192686450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753839 | CTCGGCTCACTGCAA[A/C]CTCTGCCTCCAGGAT | 11124 |
rs192686679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734522 | GGTGGATCACGAGGT[C/T]AGGAGATTGAGACCA | 11124 |
rs192688226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636762 | TTTAGTGTCCTCTCT[C/T]AGAAATTTTTTCCTA | 11124 |
rs192689337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50856848 | ATTATGTTACAGTGA[C/T]ACTATGAAATACTAT | 11124 |
rs192696921 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50839172 | ATTTTGTTGGCAACT[A/G]TGCAAGAAAAGCAGA | 11124 |
rs192699786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50821091 | TCTTCATCTATAAAA[A/T]GGAGGAAATAATGCT | 11124 |
rs192701284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771211 | AGATTTCATAACAAA[C/G]ACATCAAAAGCAATT | 11124 |
rs192703237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50946499 | GGACTTCCCTCAAAT[C/T]CTGTTAACCAACCTA | 11124 |
rs192708977 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50605638 | TTCACAGTTCCTATC[A/T]CTACAGCTTTATGCC | 11124 |
rs192712168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466271 | GAGTCAAGGATAACA[G/T]TAAGGTTTCTTGCCT | 11124 |
rs192712743 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677060 | CTATATGCACATTAG[G/T]CACTTTATAATTGAA | 11124 |
rs192714874 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50712878 | TCTTTTACCTTCAAG[G/T]TGGGGGGGCGCTGTG | 11124 |
rs192716696 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50910858 | GCCCCGCCCTGCTTC[A/G]GCTCACACTCCGTGG | 11124 |
rs192720296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50878873 | CAGTGTTAGCAAATG[A/G]TATTAGAATTACAAT | 11124 |
rs192732868 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50559175 | AGAATTGCTTGAACC[C/G]AGGAGGTGGAGTTTG | 11124 |
rs192740016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50508155 | GTAAAATGGTGCAGC[C/T]TCTCTAGAAGGTTCC | 11124 |
rs192741615 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50847792 | ATAAATTTCTCCTCA[A/G]TAAAAAAGAAAAATA | 11124 |
rs192746016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779786 | AGATAATACATTTTT[A/T]AAAAATTAGAAAAGA | 11124 |
rs192753252 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50821412 | TAGTTTTTAGCATAC[A/G]TATTAAAGGAACATA | 11124 |
rs192758574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632478 | CACATCTATTAGAAA[C/T]TGGGAACACATCTAT | 11124 |
rs192772063 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50949150 | CCTTGGATCAGAAGC[A/T]TCAGCATAACCAGGA | 11124 |
rs192773946 | snp | C/T | 0.030278 | 0.119257 | intron-variant | FAF1 | GRCh38.p7 | 1:50888379 | TCTTTCTTTCTCCTG[C/T]CTGATTGCCCTGGCC | 11124 |
rs192775149 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50914024 | TAATATTCCACACAA[C/G]AGATCAATCTCCTGT | 11124 |
rs192778996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50672279 | AACTCCTGACCTTGT[A/G]ATCCACCCGCCTCAG | 11124 |
rs192783375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852039 | TATAATGAGCTTTCC[C/T]TATATAGAATGGCAC | 11124 |
rs192784162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708490 | AGTTTGAGATGTCCA[C/T]TGAGATGTTTTGAGA | 11124 |
rs192808332 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50497759 | TTCACCATCTTGGCC[A/G]GGCTGGTCTTGAACT | 11124 |
rs192820406 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50551603 | GGCAGGCAGCATAGG[A/C]CCTTAAGAACATACT | 11124 |
rs192824607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50585209 | GCAGGTGGAGGCAAT[A/G]GTAGCATTTCTAAAC | 11124 |
rs192825700 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503531 | GCCTGAGGAGACTCA[C/G]TTGGGCCCAAGAGTT | 11124 |
rs192835926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625759 | CACTGATCAGATTAT[C/G]AACAGTCAAATATGT | 11124 |
rs192837126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453130 | ACTTCAATGAAAGAC[A/G]TGGCTGGAAAGACAG | 11124 |
rs192838696 | snp | C/T | 0.151334 | 0.229706 | intron-variant | FAF1 | GRCh38.p7 | 1:50952881 | GCCCGGCCGCCACCC[C/T]GTCTGGGAGGTATAC | 11124 |
rs192859031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50892167 | CAAGCCAGGAGTGGG[A/G]TATAATCTCCTGGTG | 11124 |
rs192859777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734148 | CATTTTTCCTACTTG[A/C]TGTCTCTTACTCCTT | 11124 |
rs192862191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50497503 | ACTAGAAATGGGAGC[C/T]TCATAGGTAAATTAA | 11124 |
rs192867812 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50858456 | TAGCCACTACCAGCC[A/G]CTCTCTGGTAGCTGC | 11124 |
rs192871865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770199 | AACCAGAACAAGAAA[A/G]GGATGCCCTCTCTCA | 11124 |
rs192880172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50812550 | ATCAGTCAGAATGGC[C/T]ATTATTTAAATCTCT | 11124 |
rs192889736 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50580227 | GAATTTTGAATAAAT[C/T]TTTAATTTATTTTCT | 11124 |
rs192891919 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50957037 | ATCCTATAAAAATTG[A/G]GATAATATAAAAAAC | 11124 |
rs192893694 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50660976 | GGTACAGGAAAAGAG[A/G/T]TGCTAAACATATACA | 11124 |
rs192895373 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | FAF1 | GRCh38.p7 | 1:50931971 | CAATTACCTCCCCCC[A/G]GGTCCCTCCCACAAC | 11124 |
rs192912981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50443560 | AAAGCACAGTGGTTA[A/C]AAAGAGTGAAGCAAA | 11124 |
rs192928316 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50487606 | TAGGGCCAATGACCA[C/G]ATCAATATACTTTTC | 11124 |
rs192931624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50766730 | ACTAAACTCACCTTA[C/T]ACCACAATCAAACCC | 11124 |
rs192943045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50810029 | GGGAGGCTGAGGCCC[A/G]TGGATCACATGAGGT | 11124 |
rs192945577 | snp | A/C/T | 0.00836003 | 0.0642105 | intron-variant | FAF1 | GRCh38.p7 | 1:50533401 | ATCATTGTAACCAAA[A/C/T]TTTTTTTTCAAGTTA | 11124 |
rs192957006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579763 | GCAAACGCCAGGAGG[A/G]AAAAATGGGGAGAGA | 11124 |
rs192973055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50611944 | CACATGAAAAGCAAA[A/G]GGCAAAATAATGACG | 11124 |
rs192981435 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50690162 | CACCATGCCCGGCTA[A/G]TTTTAAGTAGAAACT | 11124 |
rs192983520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650629 | TCTCAAAAAAATATA[C/T]AAATAAAAATAAAAA | 11124 |
rs192985422 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50930639 | AGGAGATCGAGACCA[C/T]CCTGGCTAACACAGT | 11124 |
rs192985532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50874050 | CCAAAATTTGGGGCT[C/T]AGTCTGGGAGGTTCT | 11124 |
rs192992564 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50896257 | ACCACTGCACTCCAG[A/C]CTGGATGATAGAGTG | 11124 |
rs192994046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50481965 | ATTAGATCATATATG[A/G]CTTTGGGAAGGACAA | 11124 |
rs192996636 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50728684 | TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 11124 |
rs193006455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50568632 | AATAGCATCCTTAAC[C/T]CCATTAGCATATGAG | 11124 |
rs193022135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50830401 | AGGCGTGAGCCATTG[C/T]GCCCAGCACCACAGG | 11124 |
rs193025119 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50610123 | AAACATTGATCAAAT[A/C]TTCCGTGGTTCTTAC | 11124 |
rs193042580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682747 | ATACCGAACATAAAA[C/T]TGAGAACTTCAGGGA | 11124 |
rs193046863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50905934 | TTGCTTTTGGTGTTT[C/T]AGTCATGAAGTCCTT | 11124 |
rs193053507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844871 | TGAGCAAGATAAATG[C/T]TTGAAAGGCTGTGTG | 11124 |
rs193056563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50719737 | ATCAATTTTTGTTTC[C/T]TAGAGTAGTGACCAA | 11124 |
rs193058442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872663 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGAACAC | 11124 |
rs193059481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50756830 | TCAGATCTCATGAGA[C/T]TTATTCACTATCACG | 11124 |
rs193064010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50520282 | AAGAAAAATGCCAGA[C/T]AATTCTCAGTATCCC | 11124 |
rs193070057 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50799769 | TGCATATATTCGACT[A/T]TATTATAAAAACCAA | 11124 |
rs193072153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50473733 | TGAGAAAAGGAACAA[A/T]AGTCAGCACCTGGGA | 11124 |
rs193085671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50601035 | AAAGCTGTGAACTGC[C/T]GAACTATGTAATGTG | 11124 |
rs193103200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470541 | CAAATTTGATATCCA[C/T]CACTGTTCTAGAGAA | 11124 |
rs193104711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50560313 | AATGTGGAAAACTAT[C/T]ACTTGAATATTAAGC | 11124 |
rs193130620 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50952620 | CCCAGTCTGGGAAGT[A/G]AGGAGCGCCTCTTCC | 11124 |
rs193133049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919261 | ACAGATCTGCATATA[A/T]AAAACAGTAACGGTT | 11124 |
rs193136003 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50704280 | ACAGAAACTAGGGGT[C/G]GGGGTTGAGAGGGTG | 11124 |
rs193136880 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638415 | TTCCCCCATTAAATA[C/T]GGTAGGTATTGCTTT | 11124 |
rs193138394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50885440 | CTTTATCATTATACA[A/G]TAACCTTTGTCTTTT | 11124 |
rs193139466 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50744165 | CAATACTCTCTGCAA[A/G]TTCTTAAAATATAAT | 11124 |
rs193141266 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677920 | AAAAAAAAAAAAAGA[A/G]CAACTAGTTTTTATC | 11124 |
rs193144114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50848286 | ATATGCAAAAGTAAA[C/T]TGCATGACAAAAATA | 11124 |
rs193145803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779538 | ATCTCCCTGTATATA[C/T]TGATATCTAAATATA | 11124 |
rs193148657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941968 | ACTGCCTAGCATACC[C/T]ATTTGAGAAAATGTG | 11124 |
rs193153214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50915305 | AACCTGGGAGGCGGA[A/G]GTTGCAGTGAGCCAA | 11124 |
rs193154443 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50642753 | ATGTAATTCATACTT[A/C]CTGTAATTATCAATA | 11124 |
rs193157201 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50682518 | CATGTCGTCTTATGT[A/T]ACTTTCTGTTTTGAT | 11124 |
rs193162185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50708662 | AAAATAAGTGACACA[A/G]ACAAAAGAGAGGCCA | 11124 |
rs193169521 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50750203 | TCCCACCCCAGGCCA[C/G]GTTCCTTGAAAAATT | 11124 |
rs193172958 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50788641 | CTCCCCAATTCTCCC[C/T]ATCTCACATCTCAGT | 11124 |
rs193176415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50827339 | CTTACCCCCAACTCC[A/G]TGCCCTCTGAAACAT | 11124 |
rs193194128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460156 | TTTTTCATCTCTTAT[A/T]TTATTTCCCTTTATA | 11124 |
rs193205851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50590344 | GTTTGGTAGCTTTCA[A/T]AGTACAAGTCTCCCG | 11124 |
rs193209838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545342 | TGCAGTGATGCCATC[C/T]TGGCTTACTGCAACC | 11124 |
rs193211789 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50631426 | AGTCATTTAGTAGAC[A/C]TTATCAGATTTATCA | 11124 |
rs193219314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662134 | TTCTTCTCATTAACC[A/T]TTAAAAAGACCAAGC | 11124 |
rs193227673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50698734 | TTATATCCCTCCTCA[C/T]CCTATAACTTACATT | 11124 |
rs193229329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50739306 | TACATGTGTACACGT[A/G]CATGCATATACATGT | 11124 |
rs193229667 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50887932 | AGTCATTGGTAGCTT[C/G]ATGGGGATGGCATTG | 11124 |
rs193233130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850259 | TAACTAGCTGGATTA[C/T]GAAGCTATACATACT | 11124 |
rs193234167 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50808452 | TGCCCTAATTAAAAG[A/G]CACAGACTGGCAAGT | 11124 |
rs193235875 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50776569 | CCATCAAAAAAAAGA[A/C]CAAGGTTTTTCTGAA | 11124 |
rs193257338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50448476 | ATCCACATGGAGTGA[C/T]TTCTGGATGTGTTCC | 11124 |
rs193270255 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50493252 | TAGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 11124 |
rs193284983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50686172 | TTGCTATCAACCCAC[A/T]TGAAATGTTATTCTA | 11124 |
rs193285388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50656775 | GTAATCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 11124 |
rs193286091 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50937698 | TTTTAACCACTGGAG[C/T]CAAGTTCTATATTCC | 11124 |
rs193290502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902196 | AAAGTACTTAAAGGA[C/T]TTTTTAAAACTATTC | 11124 |
rs193292466 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | FAF1 | GRCh38.p7 | 1:50723411 | TCCAAAAAAAAAAAA[A/T]AAATAAGTAGGATGA | 11124 |
rs193292947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50869405 | CTTCTACTTATTTTC[C/T]AATCATCCCATTCTC | 11124 |
rs193296563 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50760639 | GTTGTTTGAAACCAA[C/T]GAGAACAAAGACACA | 11124 |
rs193300444 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50804621 | TAAAAGCTAAAAAGA[C/T]ACATGGGAAACTAAG | 11124 |
rs199502223 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50941068 | ACACAGTCTCACTCT[G/T]TCACTCAGGCTAGAG | 11124 |
rs199503282 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50703014 | AAAAATTAAAAAAAA[-/T]ATATATATAAAATAC | 11124 |
rs199503471 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50743127 | TCTGACTCTGTACAG[A/G]AAAAGTTTGCTGCCA | 11124 |
rs199504627 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735782 | AGTACAGTGGCATGA[A/T]CTCAGCTCACTGTAA | 11124 |
rs199504654 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50811171 | TAACCCCGTCTCTAT[-/A]AAAAAAATACAGAAA | 11124 |
rs199506351 | snp | A/C/G | 1.65231e-05 | 0.00287424 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50596193 | ATGGCAGGGATAAGA[A/C/G]AGCCCTGATTCAGCA | 11124 |
rs199506503 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779995 | ACAGACAGACAGACA[C/G]ACACACACACACACA | 11124 |
rs199509684 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50826309 | TAATCCCAGCACTTT[G/T]GGAGGCTGAAGCGGG | 11124 |
rs199511430 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865836 | TAAAACTTAAAGTAT[A/T]ATAATAATAAAAGAA | 11124 |
rs199515180 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917688 | GGAAAGGAAAGGAAA[A/G]GAAAGGAAAGGAAAA | 11124 |
rs199522504 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50728141 | CACTAATATAATGCA[C/T]GGTAGGGATAAAGCA | 11124 |
rs199524443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50683584 | AAATGTTACTTTTGA[C/T]AAAACTGATAGGAAC | 11124 |
rs199537148 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50761803 | ATGCCCTCTCTCACC[A/G]CTCCTATTCAACATA | 11124 |
rs199575712 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750622 | TATCCTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs199586524 | in-del | -/AAAG | 0.067446 | 0.170804 | intron-variant | FAF1 | GRCh38.p7 | 1:50597115 | GTTGAGTTTATGGGT[-/AAAG]AAAGCAATGAGAAAA | 11124 |
rs199599205 | in-del | -/AAT | 0.0349115 | 0.127424 | intron-variant | FAF1 | GRCh38.p7 | 1:50526437 | CCCATCTCTATTAAA[-/AAT]AATAATAATATTTAT | 11124 |
rs199614408 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953151 | GGTTAAATGGATTAA[A/G]GGCGGTGCAAGATGT | 11124 |
rs199618409 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945299 | CAACATCAAAACCAT[-/A]AAAAAAAAATGGCAA | 11124 |
rs199634269 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836177 | TGTTTCTGTTTTTTT[-/G]TTTTTTTTTTTTAGA | 11124 |
rs199634797 | snp | C/T | 6.60982e-05 | 0.00574846 | missense | FAF1 | GRCh38.p7 | 1:50738918 | TAAGGACATAAAGAC[C/T]GTTGTTTTTTGGCAA | 11124 |
rs199635828 | in-del | -/TTTTTA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50782541 | AAAATGTCAAAAAAT[-/TTTTTA]TTTTTATTTTTTAAA | 11124 |
rs199637214 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499364 | ATGTTAGCTGTAGGG[-/T]TTTTTTTTTTTTTTT | 11124 |
rs199641825 | in-del | -/AAGTAACCC | 0.0193772 | 0.0965046 | intron-variant | FAF1 | GRCh38.p7 | 1:50689682 | ACAGCCAAAAGGTGG[-/AAGTAACCC]AAGTATCCATTAATG | 11124 |
rs199655087 | in-del | -/GAG | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50694422 | TTTGCTCTTGAAATT[-/GAG]TTTTCATTAAAAAAA | 11124 |
rs199662642 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601124 | CAAAAAAGCTCTTTC[-/AT]AAAATCTTAGAATCT | 11124 |
rs199664895 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50689993 | AATTACATTATATTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs199666451 | in-del | -/CTTG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50880243 | AGCTGATATTCATGT[-/CTTG]ATTAAGAAATAAGAT | 11124 |
rs199703019 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50723552 | AGAGTAGAGTGGCTA[C/T]AATGGCCTCAGTACA | 11124 |
rs199703084 | in-del | -/TATA | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50800105 | TTCAACCCCAAATAT[-/TATA]TATAGTAACTTTATG | 11124 |
rs199710646 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601733 | CTATATATATTCATA[C/T]ACACACATATATTCA | 11124 |
rs199718970 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637681 | CTCACACATATATAT[A/G]TGTGTGTGTGTGTGT | 11124 |
rs199723667 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510166 | ACGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 11124 |
rs199732708 | snp | A/G | 6.59315e-05 | 0.0057412 | intron-variant | FAF1 | GRCh38.p7 | 1:50490581 | TTTTCTTAAAATTAT[A/G]CCCCACCTCACGTTC | 11124 |
rs199744504 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931891 | AATAAATAAATAAAT[-/A]AATAATAATAATAAT | 11124 |
rs199757307 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457152 | AGAGGAGGGAAAGTG[-/A]AAAAAAAAAAAAAAT | 11124 |
rs199758536 | in-del | -/CT | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50478196 | TGAGATGGAGTTTCA[-/CT]CTGTCGCCCAGGCTG | 11124 |
rs199761587 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554384 | ATATATATATATATA[G/T]ATATATAGAGAGAGA | 11124 |
rs199783178 | in-del | -/AAAT | 0.282369 | 0.247896 | intron-variant | FAF1 | GRCh38.p7 | 1:50838557 | AGAATTATAAATTAA[-/AAAT]ATATATATTTTATAT | 11124 |
rs199783545 | in-del | -/GTG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50899687 | TGAGCTCCTGACCTT[-/GTG]ATCCACCCACCTCGC | 11124 |
rs199786316 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863177 | ATTCTGTCAGACCAC[A/G]GTAGAATAAAATTGG | 11124 |
rs199790509 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50667389 | TAAATCAATTATGCC[C/T]TATCCTGTTATTCTA | 11124 |
rs199799555 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872900 | GCGAAACTCCGTCTG[A/G]AAAAAAAAAAAAAAT | 11124 |
rs199805327 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704314 | GCAAAATTATGGCTA[A/G]AAAATTCAACCCCGA | 11124 |
rs199830442 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50699198 | TAAAAAGCAGGTGAT[A/G]TATATTCCTAAATTT | 11124 |
rs199851235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50476458 | ACTTAAGCAGGTGAA[A/G]CAAACTGTTGGAAGG | 11124 |
rs199878187 | in-del | -/A | 0.000143606 | 0.00847245 | intron-variant | FAF1 | GRCh38.p7 | 1:50714994 | TAACAGATATAAAGT[-/A]AAAAAAAAACCTGTT | 11124 |
rs199882037 | in-del | -/AG/AGAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779993 | CACAGACAGACAGAC[-/AG/AGAA]ACACACACACACACA | 11124 |
rs199883297 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50908032 | AAATTTCCCTCTACA[A/C]ACAGCTTTAAAAGTG | 11124 |
rs199900774 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573818 | CAGAGGGTTAAAAAC[-/A]AAAAAAAAAAAAACA | 11124 |
rs199911582 | in-del | -/AAGGAAGG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490385 | AGACTCTATCTCAAA[-/AAGGAAGG]AAGGAAGGAAGGAAG | 11124 |
rs199911765 | in-del | -/GACA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50798828 | TGTGGAAGACAGACA[-/GACA]TTATGTACATGTATT | 11124 |
rs199916977 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50482930 | CCTTGTCTGTGGCTT[G/T]TTTTTTCAATTTCCT | 11124 |
rs199925876 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50956640 | TATGCCAAGTCTTAA[A/G]CTGCAATCCTTAAAT | 11124 |
rs199938727 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748293 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGCCC | 11124 |
rs199964324 | in-del | -/TTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50954541 | AATAAAAAATTTTGA[-/TTT]TTTTTTTTTTTTTTT | 11124 |
rs199978603 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50711587 | CGATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 11124 |
rs199980383 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645833 | ACTCCGTCTAAAAAA[A/G]GAAAAAAAAAAGGAA | 11124 |
rs199994151 | snp | G/T | 0.000593796 | 0.0172205 | intron-variant | FAF1 | GRCh38.p7 | 1:50539762 | CAAAGTAAGTTTTGC[G/T]TTGTAGTTTAATAGA | 11124 |
rs200000793 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819047 | TACTTGTGGCATCAT[A/G]TTGGCATTCAAAAAG | 11124 |
rs200010940 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | FAF1 | GRCh38.p7 | 1:50672448 | CAGCTAATTTTTGTA[-/T]TTTTTTTTGTTTTTT | 11124 |
rs200021493 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50906988 | TGCTACCAGTTTTTG[C/T]GCATTCAGTATGATA | 11124 |
rs200027447 | in-del | -/AG | 0.0310518 | 0.120672 | intron-variant | FAF1 | GRCh38.p7 | 1:50895492 | ACTATTACAAAAAAC[-/AG]AGGAGAATACTTACA | 11124 |
rs200052941 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | FAF1 | GRCh38.p7 | 1:50584662 | AATTCTATTGCTGGA[C/T]CCAAAGAGCTATTAA | 11124 |
rs200067376 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50585902 | AAAAAAAAAAAAAAA[C/T]AAAAAAGTCTGGCAT | 11124 |
rs200070288 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50720000 | TTAAAATTAAACACA[C/T]TTTTTTTTTTTTTTT | 11124 |
rs200074665 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527278 | GTGCTATTGGCCACT[G/T]GTATATCGTCCTTGG | 11124 |
rs200107050 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50688144 | CTATCTCAAAAAAAA[-/T]AAATAAATAAATAAA | 11124 |
rs200111683 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50920017 | CATAACAAAACATGT[A/G]CAGGCCAGGCAGTGG | 11124 |
rs200130049 | in-del | -/ATA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681049 | ATAATAATAATAATA[-/ATA]CGATGATGATGATTT | 11124 |
rs200133978 | snp | G/T | 0.000732649 | 0.0191256 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50857943 | CCACTAAGTCCCAAT[G/T]ATTTTGTTCAAGCAA | 11124 |
rs200135861 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50489912 | AATATTTGTTGGCAC[A/C]AAAGGCAAAGATTAT | 11124 |
rs200142842 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872065 | GCCAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs200154325 | snp | A/C/T | 0.000119746 | 0.00773692 | synonymous-codon, missense | FAF1 | GRCh38.p7 | 1:50539626 | TTCATTAGATGATCG[A/C/T]TTTCCCATAATAATC | 11124 |
rs200156810 | in-del | -/ATA | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50551704 | ATTTCAGTAAGGCAT[-/ATA]ATAAGGTGTTCCAAA | 11124 |
rs200213992 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50691667 | CGCGATCTCGGCTTA[C/T]GCAACCTCCACCTCC | 11124 |
rs200222282 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50582107 | GTTGTTAGATATATA[C/T]CACTACACAGAATAA | 11124 |
rs200229291 | in-del | -/T | 0.282632 | 0.247861 | intron-variant | FAF1 | GRCh38.p7 | 1:50750623 | ATCCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 11124 |
rs200229352 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50680576 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11124 |
rs200236664 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50903293 | TCCCTACCCTCTAAC[C/T]CTCGAAAGAGTTACT | 11124 |
rs200240386 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50941202 | CACGCTCAACTTTTT[-/G]TTTTGTTTTGTTTTG | 11124 |
rs200247031 | in-del | -/AGTGGT | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50874824 | CCTGGGCTGGAGTGC[-/AGTGGT]AGTGGTGCAGTCACA | 11124 |
rs200268865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50516498 | GAATTTTTCTTGGAC[C/T]GAAATACCAAGCACG | 11124 |
rs200280624 | in-del | -/ATAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601705 | TTCATATATATATAT[-/ATAC]ACACACACACTATAT | 11124 |
rs200305373 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713253 | ATAATGAAACAGTTA[A/G]AAAAAAAAAAGGCAT | 11124 |
rs200308640 | in-del | -/AAAT | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50883140 | GGATGCAATTCAAAT[-/AAAT]GCCTAAGTGTCCAAA | 11124 |
rs200318373 | in-del | -/TCTC | 0.0260105 | 0.111035 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470613 | CCTACCTCTTCTGCT[-/TCTC]TCTATTTAGTATTAT | 11124 |
rs200340239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50614568 | AAATGGGCTGGGCAC[A/G]GTAGCTCACACCTGT | 11124 |
rs200348750 | in-del | -/G | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50735780 | AAAGTACAGTGGCAT[-/G]ATCTCAGCTCACTGT | 11124 |
rs200357140 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953164 | AAGGGCGGTGCAAGA[C/T]GTGCTTTGTTAAACA | 11124 |
rs200366572 | in-del | -/TTA | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50643933 | TCTCTTTTATATATT[-/TTA]TTATTTCCTCTTATG | 11124 |
rs200377893 | snp | A/G | 0.0650025 | 0.168154 | intron-variant | FAF1 | GRCh38.p7 | 1:50787989 | AGGCTTTATGGCAGG[A/G]AAAACCTTACCAACA | 11124 |
rs200384817 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50632624 | TATCTCCCAGCAGAT[A/T]CGCATGGTTCAATTT | 11124 |
rs200405044 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679012 | GAATGGCATGAACCC[G/T]GGAGGCGGAGGTTGC | 11124 |
rs200407686 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50712660 | ACTCTGTTGTAAAAG[-/A]AAAAAAAAATGCCAT | 11124 |
rs200417675 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50915922 | AAATCCTTTTTTTTT[-/C]CCCTAAAGCTGAAAA | 11124 |
rs200428938 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50496890 | GTCAAACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 11124 |
rs200434749 | in-del | -/AAGAAGAAAGAAGAAGAAGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624003 | GGAAGAAGAAGGAAG[-/AAGAAGAAAGAAGAAGAAGA]AAGAAGAAAGAAGAA | 11124 |
rs200438185 | in-del | -/AAAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931876 | AAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAT | 11124 |
rs200438935 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733479 | TATGTTGACTCTCTA[A/C]CACCCACTGTGACTG | 11124 |
rs200445983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505528 | GTCAGGATTCCTTCC[C/T]GAAAGGAGACAGATA | 11124 |
rs200446950 | in-del | -/TCAA | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50852370 | AAGCTTGCTAATAAC[-/TCAA]TCAGTCAAGTATTCA | 11124 |
rs200447097 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50888844 | TTTTGTTGTGTCTCT[A/G]CCAGGCTTTGGTATC | 11124 |
rs200449842 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714665 | AAAGGGGGTATGGAG[C/T]CCCAGCCACTCAAGA | 11124 |
rs200456232 | in-del | -/T | 0.185472 | 0.241529 | intron-variant | FAF1 | GRCh38.p7 | 1:50732894 | CAGGTTATTTACTTC[-/T]TTTTTTTTTTAGTGT | 11124 |
rs200470934 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924282 | AAAAAGGAACAATTT[G/T]AAAAAAAAAAAACAA | 11124 |
rs200473871 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50930962 | AAGTCTTAGTCTAAC[-/ATT]ATTAATTAATTACAG | 11124 |
rs200485966 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783045 | GAAAAAAACAGAAAA[A/C]TTAAATTAAAAATAA | 11124 |
rs200487575 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50703023 | AAAAAATATATATAT[-/AA]AATACACTAAAAAAA | 11124 |
rs200521344 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50669575 | AAAAAAAATTGGGGG[A/G]AAATAAGATTTCAAG | 11124 |
rs200522407 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50456078 | GACCCTGCTTTAAAC[-/A]AAAAAAAAATTTTTT | 11124 |
rs200523676 | in-del | -/TTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50474368 | TCTTCAGGCTTCGTT[-/TTT]CAGCATGAAGCCTAA | 11124 |
rs200535401 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694025 | CATGACATATATGAC[-/AT]ATATATGACATATAC | 11124 |
rs200536858 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50919645 | AGCACCTGACACCAC[A/G]TCTGGCTAATTTTTT | 11124 |
rs200541012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866902 | ACTAAACAAAAAGAA[C/T]AAATCTGGAGGCATA | 11124 |
rs200550139 | snp | G/T | 0.000399281 | 0.0141238 | missense | FAF1 | GRCh38.p7 | 1:50490644 | GAAACTGTTCTGCCA[G/T]CTCTCTCTCGTGAGC | 11124 |
rs200552011 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50761270 | AGGTATAAGGAGGAA[C/G]TGGTACCATTCCTTC | 11124 |
rs200556341 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50933060 | TCCGGCCCACAAAAC[C/T]ACTTTTCCTCCTGGG | 11124 |
rs200561079 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554386 | ATATATATATATATA[G/T]ATATAGAGAGAGAGA | 11124 |
rs200561819 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50584678 | CCAAAGAGCTATTAA[C/T]ACTCACTCATTGGAG | 11124 |
rs200567239 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50762297 | TCAATGCCATCCCCA[G/T]CAAGCTACCAATGAC | 11124 |
rs200572749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50716840 | AAGCTGGCCACCCCA[A/G]CCAGCAGTGGCGACC | 11124 |
rs200583751 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50489909 | ACAAATATTTGTTGG[A/C]ACAAAAGGCAAAGAT | 11124 |
rs200588965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50623134 | TATCAATAAGCTCAA[G/T]AAGTGCATCGAGTTC | 11124 |
rs200602479 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50824667 | TTATTGCAGCACTAT[G/T]CACAACAGCCAAGAT | 11124 |
rs200607198 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50865233 | GAACACTTTTACACT[C/G]TTGGTGGGACTGTAA | 11124 |
rs200610125 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant | FAF1 | GRCh38.p7 | 1:50782984 | CAACAATACTGAGTG[-/T]TTTTTTTAAAGATCA | 11124 |
rs200611700 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50533401 | ATCATTGTAACCAAA[-/T]TTTTTTTTCAAGTTA | 11124 |
rs200628409 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931888 | CAAAAATAAATAAAT[A/T]AATAATAATAATAAT | 11124 |
rs200690170 | snp | C/T | 0.00150793 | 0.027417 | intron-variant | FAF1 | GRCh38.p7 | 1:50857884 | AAAGACATTCAAGAA[C/T]TCATAAAATTTGATT | 11124 |
rs200690596 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447376 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 11124 |
rs200710823 | snp | A/C/G | 0.00011026 | 0.00742413 | utr-variant-3-prime | FAF1 | GRCh38.p7 | 1:50441436 | TTCCACCGCTGGGCC[A/C/G]TGTTTACTCTTTTGC | 11124 |
rs200713916 | in-del | -/TTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50822772 | TCTTTCTTTCTTTCT[-/TTC]TTTTTTTTTTTTTTT | 11124 |
rs200717353 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50841756 | AGCCAGATAGTAAAA[-/T]TTTTTTTAAGTTATT | 11124 |
rs200717683 | in-del | -/AGAGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922493 | AAAAAGAAAAGAGAG[-/AGAGA]AGAGAAGAGAAGAGA | 11124 |
rs200730738 | in-del | -/TTGA | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50880244 | GCTGATATTCATGTC[-/TTGA]TTAAGAAATAAGATT | 11124 |
rs200752590 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591675 | GAGACTCCATCTCAG[-/AA]AAAAAAAAAAAAAAA | 11124 |
rs200776711 | snp | A/T | 3.29772e-05 | 0.00406048 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788090 | GTTGCCTTTCTACAA[A/T]CTGCCTGGATGGCAT | 11124 |
rs200778776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705345 | GGCATACTGCCCAAG[A/G]GCAGGATGGAGCTGC | 11124 |
rs200779505 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | FAF1 | GRCh38.p7 | 1:50763093 | AACCCTGTCTCTACT[-/A]AAAATACAAAAAAAT | 11124 |
rs200804864 | snp | A/G | 0.00199802 | 0.0315439 | missense | FAF1 | GRCh38.p7 | 1:50490593 | TATGCCCCACCTCAC[A/G]TTCCTCTTCTTGTTC | 11124 |
rs200811727 | snp | G/T | 0.0569829 | 0.158885 | intron-variant | FAF1 | GRCh38.p7 | 1:50554392 | ATATATATATATATA[G/T]AGAGAGAGAGAGAGA | 11124 |
rs200819356 | in-del | -/TT | 0.0444908 | 0.142359 | intron-variant | FAF1 | GRCh38.p7 | 1:50614168 | TCAGATCCAAAACTC[-/TT]TTCAAAAATATTTTG | 11124 |
rs200832505 | in-del | -/A | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50824565 | ATATAGAGGTTCCTC[-/A]AAAAAACTAAAGACA | 11124 |
rs200848241 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50815612 | TTTTTAAGTTCTTTG[-/A]GAAATCTCTAAACTG | 11124 |
rs200867870 | in-del | -/TTTC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449482 | TTGGGGGAACAACTT[-/TTTC]TTTCTTTTTTTTTTT | 11124 |
rs200868274 | in-del | -/C | 0.0197687 | 0.0974348 | intron-variant | FAF1 | GRCh38.p7 | 1:50692211 | AGAAAACAACAACAA[-/C]CCCCACATATCCAGC | 11124 |
rs200870062 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50534610 | CCCTGCCCACATCTT[A/T]AAAAATGGTCACCTT | 11124 |
rs200875259 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742057 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 11124 |
rs200883496 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50901558 | TAAAAATTTAAAAAG[-/A]AAAAAAAAAACTGTT | 11124 |
rs200887556 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50760211 | AGTGACCTACAAAGA[A/G]ACTTAGACTCCCACA | 11124 |
rs200893646 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | FAF1 | GRCh38.p7 | 1:50804017 | AGATACAGAAGCAAA[-/G]GAAAATTCCAGATTC | 11124 |
rs200914643 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50703595 | AATTAACTTAAAGGG[-/A]AAAAAAGGAAAAAGG | 11124 |
rs200916356 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645834 | CTCCGTCTAAAAAAA[A/G]AAAAAAAAAAGGAAG | 11124 |
rs200940170 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50776523 | GAAATAAGCAGAGGA[-/T]TTTTTTTTAGTTGAA | 11124 |
rs200940717 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527868 | CTCTCTCCCTCTCTC[C/T]CTCTCTCTCTCTCTC | 11124 |
rs200979025 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836178 | TGTTTCTGTTTTTTT[G/T]TTTTTTTTTTTAGAC | 11124 |
rs200982335 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | FAF1 | GRCh38.p7 | 1:50541778 | AGAGAGAAGAGAAAT[-/A]AAAAAAAAAGGGAAA | 11124 |
rs200989462 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50485696 | AAAAAAAAAAAAAAA[A/C]CCAAAAAAACAAAAA | 11124 |
rs201002813 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50732231 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 11124 |
rs201015521 | snp | C/T | 8.24531e-05 | 0.00642026 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50584713 | TCTCAAGGCAGATGA[C/T]GCCATGCCAAATACT | 11124 |
rs201038150 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922496 | AAGAAAAGAGAGAGA[A/G]AAGAGAAGAGAAGAG | 11124 |
rs201041674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50867863 | GAAGTCATTATATGA[A/G]AAAGACTCTTGCACA | 11124 |
rs201041770 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50723394 | ACAGAGCAAGACTGT[-/C]CTCCAAAAAAAAAAA | 11124 |
rs201089417 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50665635 | TCTCTGGCTGTTTTT[A/C]CACTACCAAGATAGC | 11124 |
rs201090052 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50906989 | GCTACCAGTTTTTGT[C/G]CATTCAGTATGATAT | 11124 |
rs201099684 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672034 | CTTTTTTTTTTTTTT[A/T]TTATTTATTTACTTA | 11124 |
rs201103657 | in-del | -/AT | 0.0123036 | 0.0774623 | intron-variant | FAF1 | GRCh38.p7 | 1:50585370 | ATAATAATGTTTTAC[-/AT]ATGAGTTGTAATAAT | 11124 |
rs201107021 | in-del | -/A | 0.0298908 | 0.118541 | intron-variant | FAF1 | GRCh38.p7 | 1:50689583 | GCGAGACTCCGTCTG[-/A]AAAAAAAACAAAAAA | 11124 |
rs201111151 | in-del | -/TTTATTTA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717988 | TCAAAAATACAATCC[-/TTTATTTA]TTTATTTATTTATTT | 11124 |
rs201114342 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677960 | AGTTCTTGCCATCTT[C/T]CTTGTATTCTATTTA | 11124 |
rs201116160 | in-del | -/TGTTTA | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50739391 | ATATACATATATGTG[-/TGTTTA]TGTGTATGTGTATAC | 11124 |
rs201116775 | snp | C/T | 1.72603e-05 | 0.00293766 | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959855 | AGCGAAGCGCGCACC[C/T]GGGAGGCAGACGGCA | 11124 |
rs201118983 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50703013 | AAAAATTAAAAAAAA[-/A]TATATATATAAAATA | 11124 |
rs201130072 | in-del | -/AAAGGAAAGGAAAGG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917625 | GAAAAGGGAAAGGAA[-/AAAGGAAAGGAAAGG]AAAGGAAAGGAAAGG | 11124 |
rs201130108 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50586795 | CAGTGCTTGAGTTCC[C/T]GCTGTGTTTCAGGTA | 11124 |
rs201134207 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50740029 | AGGAAATGCACTTAT[C/T]AACAGATATTTTTTG | 11124 |
rs201145365 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50621391 | GATCTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs201153373 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50639593 | TAACTCTTTTTGTTC[-/T]TTTTTTTTTGTCTTC | 11124 |
rs201156790 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50614750 | AGGCTGAGGCAGGAG[A/G]ATCACTTAAACCTGG | 11124 |
rs201168076 | snp | A/G | 4.98674e-05 | 0.00499312 | missense | FAF1 | GRCh38.p7 | 1:50596213 | CTGATTCAGCAAGAC[A/G]CATCTGCAAAAAGTA | 11124 |
rs201188163 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499364 | TGTTAGCTGTAGGGT[-/G]TTTTTTTTTTTTTTT | 11124 |
rs201193358 | in-del | -/GCATG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735776 | GCTTAAAGTACAGTG[-/GCATG]ATCTCAGCTCACTGT | 11124 |
rs201215270 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50862104 | CCCACAGAAAGCAAC[-/G]AAAAAAAAAAACACA | 11124 |
rs201218960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50954644 | CTCCCAGGTTCAAGT[C/G]ATTCTCCTGCCTCAG | 11124 |
rs201226659 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929506 | CACACTGTTTATATT[-/A]TATCTTTTGGTAACA | 11124 |
rs201229513 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917683 | GGAAAGGAAAGGAAA[A/G]GAAAGGAAAGGAAAG | 11124 |
rs201243572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50804467 | AGGAGGAAAAAGACT[C/G]GGAAAGTGTTACAGA | 11124 |
rs201252253 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924283 | AAAAGGAACAATTTG[A/G]AAAAAAAAAAACAAG | 11124 |
rs201255813 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748306 | TTCGAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 11124 |
rs201261557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609287 | CCTGGCATAGCTTGC[C/T]ACACCGCCATTTCAC | 11124 |
rs201261803 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50697787 | AAATCTTTTTTCTCT[-/A]AAAAAAAAAGTTTTT | 11124 |
rs201264671 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503128 | ACAGGTATGAGCCAC[G/T]GCACCTTGCTCTTAT | 11124 |
rs201295380 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50616682 | ATTTTTGTATACTGA[-/T]TTTTTTTTTTTTTTT | 11124 |
rs201321615 | in-del | -/CAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50481200 | CATTGCTGAAAAAAG[-/CAA]AAAAAAAGTAAACCT | 11124 |
rs201344006 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50600526 | CCACATATACACACA[-/C]AAAAAAATTAAAATA | 11124 |
rs201351748 | snp | A/G | 0.000605865 | 0.0173944 | intron-variant | FAF1 | GRCh38.p7 | 1:50567280 | TATCCACTAATGTAA[A/G]ATTTCTTAAATTTTA | 11124 |
rs201358083 | snp | A/G | 0.0003473 | 0.0131731 | intron-variant | FAF1 | GRCh38.p7 | 1:50959733 | GAAACCCACGAGGTT[A/G]GAAGTGGGAGGGGAA | 11124 |
rs201378103 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50794026 | ATATTCTCAAATCTG[-/A]AAAAAAACTGAAATG | 11124 |
rs201378113 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724821 | CTAAGTTCTCTACCA[-/T]TTTTTTTACCCATTG | 11124 |
rs201403662 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717001 | CATTCTTGAAGTCAG[A/C]GAGACCACCAACCCA | 11124 |
rs201412517 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50751151 | CACCCATTTCATGTT[-/A]AAAAAAAAAAAGAGC | 11124 |
rs201423797 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50887835 | CAGCTTTGTTCTTTT[G/T]GCTTAGGATTGTCTT | 11124 |
rs201440581 | in-del | -/TAAATAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50882601 | AGCAAGACTCTGTCT[-/TAAATAAA]TAAATAAATAAATAA | 11124 |
rs201450132 | in-del | -/TC | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50521777 | TATCATCAATTGTGT[-/TC]TGTCATTACATGGCA | 11124 |
rs201451987 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530273 | TGTGTGTGTGTGTGT[A/G]TGTATGTATATATGT | 11124 |
rs201457467 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684147 | TGCCAAAAACTTAGT[-/A]AGTAGCAAAGTCATA | 11124 |
rs201466386 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573832 | CAAAAAAAAAAAAAA[A/C]AAAACAAAGCCTTCC | 11124 |
rs201510338 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50670127 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 11124 |
rs201543043 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50949679 | CCAGTAAGACTTTAT[C/T]TACAAAAAAAGGTGG | 11124 |
rs201545372 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735781 | AAGTACAGTGGCATG[A/T]TCTCAGCTCACTGTA | 11124 |
rs201558397 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50782386 | TGTGTGTGTTCGTGT[C/G]TTAGTTTTTAACAGA | 11124 |
rs201558823 | in-del | -/TCTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672014 | TGTTGTCCAGGGTGG[-/TCTT]TCTTTTTTTTTTTTT | 11124 |
rs201561229 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50941033 | TTTGGGGTTTTTTTG[G/T]TTTTTTTTTTTTTTT | 11124 |
rs201562009 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50822774 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs201565832 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601729 | ACACTATATATATTC[-/AT]ATATACACACATATA | 11124 |
rs201569952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895625 | CATCCCTGATGAACA[C/T]TGACGCAAAAATCCT | 11124 |
rs201575424 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769726 | AGATACAGAAAAGGC[C/T]TTCAATAAAATTCAA | 11124 |
rs201575512 | snp | C/G | 0.00036251 | 0.0134582 | intron-variant | FAF1 | GRCh38.p7 | 1:50490584 | TCTTAAAATTATGCC[C/G]CACCTCACGTTCCTC | 11124 |
rs201582667 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714345 | TGTCTCTACTAAAAA[-/T]TTAAAAAAAAAAAAA | 11124 |
rs201585272 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50785620 | TATACAAAAAAAAAA[-/A]GGAAAGAAAAGAAAA | 11124 |
rs201593653 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50635728 | TCAATTGTATAGATG[C/T]CATTTAGCTCACTCA | 11124 |
rs201597104 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50654763 | AAATGTTTTTGCCTT[A/G]AACATTTCATTAGTA | 11124 |
rs201599977 | in-del | -/ATAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556841 | ACCCCTGTCTCAAAC[-/ATAAA]ATAAAATAAAATAAT | 11124 |
rs201602872 | in-del | -/AG | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50517098 | AGAGATTTATGAAAA[-/AG]AGAATTTAAGGCAGT | 11124 |
rs201603938 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50776957 | GAAGTTTGGTGATTT[-/A]AAAAAAAAATATACA | 11124 |
rs201629986 | in-del | -/TAA | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50555611 | TAAAAAGTCAAAAAC[-/TAA]TAGATGTTGACACAG | 11124 |
rs201670630 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50881696 | TGTTTTCCATATAGC[-/A]AAAAAAAACAAGCTT | 11124 |
rs201675426 | in-del | -/AAC | 0.00676609 | 0.0577691 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960870 | GTAGTTATGAGAAAT[-/AAC]AACCTCGAGTTAATA | 11124 |
rs201701540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872644 | GCTCATGCCTATAAT[C/T]CCAGCACTTTGGGAG | 11124 |
rs201701725 | snp | A/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961049 | ATTTATTTATTTATT[A/T]TTTTGAGACGGAGTC | 11124 |
rs201724827 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701402 | ACAAAACAAACAAAC[A/C]AAAAAAAACACCCAA | 11124 |
rs201742480 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50889235 | TCATTTTTTATTGCA[C/T]CTATTTGATTCTTCT | 11124 |
rs201752415 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836951 | GTGTATGTTATGTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs201758729 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50489911 | AAATATTTGTTGGCA[A/C]AAAAGGCAAAGATTA | 11124 |
rs201764077 | in-del | -/AG | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50917437 | AAAATAGAAACCAGC[-/AG]AGATTTTTGCAGCAA | 11124 |
rs201764267 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50623668 | CAAATGAGGCCAGGT[A/G]TGGTAGCTCATGCCT | 11124 |
rs201769100 | snp | C/T | 0.000513343 | 0.0160127 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788003 | GAAAAACCTTACCAA[C/T]AGTACAGGTGTCTTC | 11124 |
rs201770728 | snp | A/G | 6.59924e-05 | 0.00574385 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788153 | TAGGAGCTGAAGCTG[A/G]ATGACTTGCTGGATT | 11124 |
rs201771551 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50870943 | AAGGTTTTTTTGCAC[A/C]AAATAGCCACATTGT | 11124 |
rs201808082 | snp | G/T | 0.00182796 | 0.0301768 | missense | FAF1 | GRCh38.p7 | 1:50744728 | CTTTTAACAGCATTT[G/T]GGACACAGGTATCTG | 11124 |
rs201818355 | snp | A/G | 0.000347939 | 0.0131852 | intron-variant | FAF1 | GRCh38.p7 | 1:50584633 | TCTTCATAAGTTTGT[A/G]TACTAGAAGAAAGAA | 11124 |
rs201828120 | in-del | -/TAAG | 0.0287284 | 0.116357 | intron-variant | FAF1 | GRCh38.p7 | 1:50599582 | ATCAGTAAAAATTAT[-/TAAG]TAATTTAATTTATTT | 11124 |
rs201829971 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50918878 | TGACTTTTTAATGAT[C/T]GCCATTCTAACTGGT | 11124 |
rs201834226 | in-del | -/CTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789739 | TTCTCTTTCTCAACC[-/CTT]CTACTCTCCTTTACT | 11124 |
rs201835470 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694009 | TGTCATTATATATAT[-/AC]ATGACATATATGACA | 11124 |
rs201844725 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808654 | TTAAATCAATAAAGA[-/T]TTTAAAAAAAAAAAA | 11124 |
rs201846887 | in-del | -/ATC | 0.0275645 | 0.114116 | intron-variant | FAF1 | GRCh38.p7 | 1:50663839 | TAAATATAATTAATA[-/ATC]ATTTGTTACAGAAAT | 11124 |
rs201862176 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672037 | TTTTTTTTTTTTATT[A/T]TTTATTTACTTATTT | 11124 |
rs201862964 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50700242 | GCTTTGAAAAGGGGG[-/CT]CTGTGTGTAATGGGT | 11124 |
rs201874092 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50760499 | TGTCTCTCAGACCAC[A/G]GTGCAATCAAACTAG | 11124 |
rs201876011 | snp | C/G | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459951 | AATGGTTTTATGAGG[C/G]CAAGAATTCTGTCCT | 11124 |
rs201878159 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50498823 | CCACTGCACTCCAGC[A/C]TGGGCGACAGAGCGA | 11124 |
rs201886577 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638744 | CCACCACGCCCAGCC[C/T]AGCTATTGCTTTTTC | 11124 |
rs201889646 | in-del | -/T | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50735782 | AGTACAGTGGCATGA[-/T]CTCAGCTCACTGTAA | 11124 |
rs201892383 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50641541 | TGTTTGGTTAGTGAT[-/A]ATATTAATTACAATC | 11124 |
rs201936599 | snp | C/T | 0.00129326 | 0.0253961 | intron-variant | FAF1 | GRCh38.p7 | 1:50858032 | GCATTTTACATATAA[C/T]TTTAGAAATAGGGAG | 11124 |
rs201944649 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885342 | CTCTCTCTCTCTCTC[C/T]CAATATTTGCTTTAC | 11124 |
rs201947438 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50682015 | TTTTTGTATTTTTTT[-/T]GTAGAGTCAGGGTCT | 11124 |
rs201956795 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490539 | TTAACAGCTTCAGTA[G/T]CAAATACAACCCAGC | 11124 |
rs201959810 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830675 | TTTTTTTTTTTTTTT[A/T]CCAACTCCAATGGCT | 11124 |
rs201964842 | in-del | -/AAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931889 | AAAAATAAATAAATA[-/AAT]AATAATAATAATAAT | 11124 |
rs201969293 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50696664 | ACTGGCATTTTTTTT[-/T]AAATTCTATTTTGAA | 11124 |
rs201969680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469541 | GAAGATTTTATATGC[C/T]ATGGTAAGGAGTTTG | 11124 |
rs202015233 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50485682 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAAAAAAAC | 11124 |
rs202018603 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468769 | GGCCTAATTTTTGTA[-/T]TTTTTTAGTAGAGGC | 11124 |
rs202030118 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50862751 | CTATTCTTATATGAG[-/A]AAAAAAACAAACTTT | 11124 |
rs202033561 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642284 | TTATGTTTAGTGTTT[C/G]GATGGCAAATATTTT | 11124 |
rs202037620 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50816044 | AAAAAAAAAAAAAAA[-/T]TTTAAAAAAGCCATT | 11124 |
rs202040929 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953644 | CTTGGGAGGCTGAGG[C/G]AGGAGAATCGCTTGA | 11124 |
rs202042404 | snp | C/T | 1.65078e-05 | 0.00287291 | missense | FAF1 | GRCh38.p7 | 1:50535422 | TCTCCATTGCAGCCA[C/T]GAGTCTCATCATTAA | 11124 |
rs202054576 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788021 | TACAGGTGTCTTCAA[G/T]TACCACATCAACATT | 11124 |
rs202055478 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590897 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 11124 |
rs202064951 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50720001 | TAAAATTAAACACAC[-/T]TTTTTTTTTTTTTTC | 11124 |
rs202099538 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924279 | ACCAAAAAGGAACAA[A/T]TTGAAAAAAAAAAAA | 11124 |
rs202110457 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750423 | AACTCACTCATGAGT[G/T]TAGCCAAATATATAC | 11124 |
rs202132117 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50676464 | GCCACTTATTTCAGT[-/A]AAAAAAAAAGAAAAA | 11124 |
rs202138904 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661865 | GGCCTTCTTTTCCTC[G/T]TGTTTTTAAAAGTAT | 11124 |
rs202140280 | in-del | -/TGGCA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735774 | AGGCTTAAAGTACAG[-/TGGCA]TGATCTCAGCTCACT | 11124 |
rs202143220 | snp | A/G | 0.000399281 | 0.0141238 | missense | FAF1 | GRCh38.p7 | 1:50567140 | TTTTGACTCAGATAA[A/G]AAACAATGGATTCAG | 11124 |
rs202143541 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50856095 | CAAAATTAGTGGACA[C/T]GAACCAATAGGAAGC | 11124 |
rs202156659 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50473533 | AGGCTGATCTTGAAC[A/G]CTTTGATAATGGTTC | 11124 |
rs202175527 | snp | A/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961050 | TTTATTTATTTATTA[A/T]TTTGAGACGGAGTCT | 11124 |
rs202216513 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50761255 | GCCGAATTCTACCAG[A/T]GGTATAAGGAGGAAC | 11124 |
rs202217491 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50952616 | GCCGCCCAGTCTGGG[-/A]AGTGAGGAGCGCCTC | 11124 |
rs202217820 | in-del | -/GCA | 0.0205511 | 0.0992634 | intron-variant | FAF1 | GRCh38.p7 | 1:50735776 | GCTTAAAGTACAGTG[-/GCA]TGATCTCAGCTCACT | 11124 |
rs202225053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50527902 | CTCTGAGACAGGGTC[G/T]TACTCTTGCCCAGGC | 11124 |
rs202229758 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922497 | AGAAAAGAGAGAGAG[A/G]AGAGAAGAGAAGAGA | 11124 |
rs202231293 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50799989 | TTAGGAAGGAAATAG[C/T]TGAAGAATATTACTA | 11124 |
rs207460119 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50584022 | TTTAGGATTTCAATG[C/T]TTTCTTGAAATAGAC | 11124 |
rs367550319 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50605864 | TATAGTTACTCAGAG[G/T]TGATAACTTATTCAA | 11124 |
rs367553866 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819779 | CGTATATATATATAC[A/G]TATATATACATATAT | 11124 |
rs367566293 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50594762 | TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 11124 |
rs367569585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50624971 | CAATGGCATGATCTC[A/G]GCTCACTGAACCCTC | 11124 |
rs367572716 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50600001 | ATCATGTTGCTGCTT[A/T]AAAAGTTTCAGATTT | 11124 |
rs367577010 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573436 | ATACGTGAGAGTGAG[-/A]AAAAAGAAGAGTAAA | 11124 |
rs367593248 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50504782 | TGCTGATCCAATGAT[A/T]AGACCCTGGATGACT | 11124 |
rs367595496 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683893 | GCCAAGATCGCGCCA[C/T]TGCACTTCAGCCTGG | 11124 |
rs367597752 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545277 | CCTAATTATAGCTAC[-/AT]ATATATATATATTCG | 11124 |
rs367626710 | in-del | -/GCT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950810 | TGACAGCCAAGCACT[-/GCT]AATTTATTTTATACG | 11124 |
rs367627801 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50882755 | CTTTGGGAGGCCAAC[A/G]TGGGCAGATCACCTG | 11124 |
rs367636047 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725612 | AGGTGTGTGCCACCA[G/T]GCCCAGCTAATTTTT | 11124 |
rs367645581 | in-del | -/AAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50778674 | GAACAAACTGAAGAG[-/AAG]GAGGAAGGGGAGGGG | 11124 |
rs367649130 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50759782 | AACAGTGTAAAAGTG[C/T]TCCTATTTCTCCACA | 11124 |
rs367656097 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50744096 | TGTGTAAAAAATGTT[A/G]TATCTGAGGTTGCTA | 11124 |
rs367679277 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766705 | AAAGGAAGGGAAACA[A/G]AGTCAGTTGACTAAA | 11124 |
rs367686180 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50834063 | GACTGGATCATCGGG[C/T]GGATTTCCCCCTTGC | 11124 |
rs367691732 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50787409 | TTATAAAAAGAGTTT[C/G]ATGAAGGGAGTCTGT | 11124 |
rs367694333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50840592 | CAAAATACATCTAAC[C/T]ATATACTTTAGATTT | 11124 |
rs367700566 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50653639 | GGGAGGCCGAGGCAG[A/G]CTGGTCACCTTAGGT | 11124 |
rs367707031 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50537084 | AGGTATGTGCCACCA[C/T]ACCTAACCAATGTAG | 11124 |
rs367708046 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50853768 | CGTGTGTAAAATAAG[C/T]GGCAGAGCATCTTCT | 11124 |
rs367715295 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50506806 | AGAAAAGAAGTGACC[A/G]TATATACAACAAGAG | 11124 |
rs367739340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50486292 | CTATTTTAATTCACC[C/T]AAGATTCGCCAAAAT | 11124 |
rs367759550 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543465 | TGAGTTTAAAAGAGC[C/T]TCAGGTATAAAGTGG | 11124 |
rs367763648 | in-del | CC/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576641 | CCGCACCGCCCCCCC[CC/T]CGCCACCACCCCTGC | 11124 |
rs367768828 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602963 | TTCTCACAATAACTC[G/T]GCCAGGTAAGGATTA | 11124 |
rs367770718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50572013 | GTGTTAAAACTATAG[C/T]ATAAAATAATTTCCT | 11124 |
rs367774505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50527285 | TGGCCACTTGTATAT[C/T]GTCCTTGGAGAAATA | 11124 |
rs367777542 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50625957 | CAGGAGAAAGTTATA[A/C]GAGTCTAAACTATGG | 11124 |
rs367781039 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591329 | TGCACAGCAGAGCGC[G/T]CTTCACTAAACTGTG | 11124 |
rs367788698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50654814 | CATCAAGAAAAAAAC[C/T]AAGTCAAAGTCAAAT | 11124 |
rs367793740 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50663868 | AAATTCTAAAAATGT[G/T]GCAATTTCATTTGGA | 11124 |
rs367804145 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50615687 | ATGTCTGTTTATATC[C/T]TTTATCCATTTTTTA | 11124 |
rs367818697 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50620619 | TGTCTGGAGGTAAGG[C/G]GACACTGGCTTTTTC | 11124 |
rs367830591 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50448275 | CTGTTGAAGTGTGAT[C/G]CCAGGGAGGGATACC | 11124 |
rs367839991 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958570 | GTAGTCCCAGCTACT[A/C]GGGAGGCTGAGGCAG | 11124 |
rs367843594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50681609 | GCCCCCCGAGTTCAA[A/G]TGATTCTCCTGCCTC | 11124 |
rs367843933 | snp | A/G | 1.85334e-05 | 0.00304407 | intron-variant | FAF1 | GRCh38.p7 | 1:50452063 | TATTAAGAATGGAAT[A/G]GGGAGGAAAAAACCG | 11124 |
rs367865849 | in-del | -/AGAAGAAAGAAGAAGAAGAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624024 | AAAGAAGAAGAAGAA[-/AGAAGAAAGAAGAAGAAGAA]CCACAAATACAAATG | 11124 |
rs367866473 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50813014 | TAAGTAGGAGGTAAA[C/T]ACTCAGTTACATAGA | 11124 |
rs367869283 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50790905 | TTTTAAAGATTAGAA[C/T]AGAAATTATCAGTAT | 11124 |
rs367875347 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50857802 | GATATGGCATTTAGA[C/T]TTTATTAACTCAGCT | 11124 |
rs367877788 | snp | C/T | 0.000454418 | 0.0150666 | intron-variant | FAF1 | GRCh38.p7 | 1:50539584 | TCTCCTTGTGACATG[C/T]ACTTTACCTTGTATC | 11124 |
rs367880161 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50841599 | CTTTCTTTGCCTTTA[C/G]GGTTGTAGCAAAAAG | 11124 |
rs367883457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881908 | TATACAGGTAAAGCA[C/T]AAATTTTTCAGCTGG | 11124 |
rs367902425 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50826546 | AGAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 11124 |
rs367902636 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875668 | ATGTTGGTCAGGCTG[A/G]TCTCGAACTCCTGAT | 11124 |
rs367904455 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960251 | TTCCTCCCTGGCCGC[C/T]GCCTCCGCCCCTGGT | 11124 |
rs367937376 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50605845 | TTGAATGTTATACTA[A/G]CCATATAGTTACTCA | 11124 |
rs367957992 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50738268 | GACCAACATGGAGAA[-/A]CCCCATCTCTACTAA | 11124 |
rs367969392 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50890196 | AACCCCTGCCTTTTT[C/T]TGCTTTCCATTTGCT | 11124 |
rs367975188 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50631595 | AAAGGAGAAAGTTCT[G/T]GACTTAATAAGAAAA | 11124 |
rs367981371 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649835 | CTGGGTATGATGGCA[A/C]GTGCCTGTAGTCCTA | 11124 |
rs367981830 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50594520 | GTTGGGCATGAAAGT[A/G]CTGTTTGTAGCCATG | 11124 |
rs367986474 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562244 | TATCTTATCCCTGCT[C/T]CACTGTCTGCCTGTA | 11124 |
rs368007138 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672571 | TATAGGCGTGAGCCA[C/T]GGCGCCTGGCCAGCA | 11124 |
rs368017165 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622864 | ACACCAGGAAGCAGT[G/T]GTAGGCACAATTGGT | 11124 |
rs368041236 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50669171 | TTCACATACTTTTCT[A/G]GTTGGGGATGCCCTC | 11124 |
rs368062963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694444 | CATTAAAAAAATCAG[G/T]AATCTTACTAATTAT | 11124 |
rs368064681 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50810208 | TGCAGTGAACCAAGA[C/T]TGCACCATTGCACTC | 11124 |
rs368067282 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766123 | ATGAGACCTAGCCCA[G/T]CTCAGAGTAGAAACA | 11124 |
rs368072235 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50832344 | ACCACTGTCCAGTAC[A/T]GGCACAGAATCCAGC | 11124 |
rs368089124 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50698687 | ACAAATTTCATTGTA[A/T]ATTTTGCTGGTGGAA | 11124 |
rs368091865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488821 | TAATTGATAAGCATA[C/T]GTAAAGCAGCTAGCA | 11124 |
rs368098538 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50679499 | GATGATCCTGCCTCT[A/C]TACTCAGACATTTAA | 11124 |
rs368110329 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748863 | AAGAAAAAGAAGAGT[G/T]GGGGGAGAACTTAAG | 11124 |
rs368117616 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50455537 | AGGACCAGGAAGCCA[A/G]TGGTTTTGTTCTAGT | 11124 |
rs368118564 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769453 | ATTTTATGAGGCCAG[C/T]ATCATCCTGACACCA | 11124 |
rs368148104 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50823751 | AAAGAGATTACCCAG[A/C]GAAAACAGTTAAAAA | 11124 |
rs368153348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549121 | AAGTTATTCTTTACA[C/G]CATGCTTGCCACTGT | 11124 |
rs368157044 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50853108 | TATTATCAATGGTTA[A/G]TCTATTCATTCATAA | 11124 |
rs368159655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845868 | TGGCTCATGCCTGTA[A/C]TCCCTGCACTTTGGG | 11124 |
rs368159726 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50571352 | TTAAAGTAACAGAGA[G/T]CTCTGTTCTAAATCC | 11124 |
rs368159868 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50547231 | AATATAATGCCTCAC[A/G]ATGCAAATGCACATA | 11124 |
rs368170216 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50517726 | AAATAAGATATTTTT[C/G]CAATTAGCATATGAC | 11124 |
rs368176358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50920367 | AAAAACAGCAGGCAT[C/T]ACTGCTCCCAAAAAG | 11124 |
rs368177135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50873307 | TTTACCGCATTGGTC[A/G]GGAACTGAGCCTAAA | 11124 |
rs368189268 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50930632 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 11124 |
rs368190773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50444635 | ATTTTCTTGTTCTTC[A/G]GTCATCATCATAGCA | 11124 |
rs368192527 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645987 | ATTAGATATAATTGT[A/G]TGAAACTTCTAATCT | 11124 |
rs368199029 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683657 | AATGTTTTTGGCCGG[A/G]TGCAGTGGCTCATAC | 11124 |
rs368209670 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50506416 | GCCTTTGTCCATCCT[G/T]TATCCTTGGCCTGGA | 11124 |
rs368216269 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50681572 | GAGTGCAATGGCGCA[A/G]TCTCGTCTCACTGAA | 11124 |
rs368220269 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50523261 | GAGTCCCTGTTTTCA[A/G]TTCTTTTGGGTATAT | 11124 |
rs368220868 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50613890 | GACCTCAAGGTCAAG[A/C]GATCAAGACCGTCCT | 11124 |
rs368228869 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50653848 | GTACTCCAGACTGGG[C/T]GATAGAGCAAGATTC | 11124 |
rs368229489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50746725 | GCTGCAGAAGTTTAC[A/G]TAAGTAAAGAAAAGC | 11124 |
rs368232180 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50712702 | TAATTTGCAAAGACA[C/T]TTTTGCTAAAATGTT | 11124 |
rs368263847 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938174 | AGCTCAGAACATCCT[A/G]TCTGACATTACTATA | 11124 |
rs368264801 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467060 | TGGACCCACTGCATG[A/G]ACTGCAGTATGAGGA | 11124 |
rs368273895 | in-del | -/GGCA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694302 | AGGCAAAGGCAGGCA[-/GGCA]TGTAAATATAATGTG | 11124 |
rs368285599 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50671032 | TAGAATGTATGTAAA[C/T]AATACCTTATTTGAA | 11124 |
rs368296424 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50441753 | ATAGTCAAGTTTGGT[A/G]GAGGTACCTTTCTTG | 11124 |
rs368304357 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458757 | TAGCTTAGAAATGCT[C/G]AGCATTTACTATGCT | 11124 |
rs368331190 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493157 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11124 |
rs368332513 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50837189 | TCTTGATCTCCTGAC[C/G]TCGTGATCTGCCCAT | 11124 |
rs368336200 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50790331 | ATTTTTAGTAGACAC[A/G]GGCTTTCACTGTATT | 11124 |
rs368341015 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50523798 | AGTCTCCCATTGATG[A/G]GCATTTAGGTTGATT | 11124 |
rs368348724 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50826164 | ATGTAAAGATAAATA[C/T]GAAAAATTTTAAAAA | 11124 |
rs368350043 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50679183 | TAACTGCTATATGTG[A/G]CAACAAAATTACTGA | 11124 |
rs368352448 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50948676 | TAGCTGGGACTACAG[A/G]TGCACGCCACCATAC | 11124 |
rs368353455 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881479 | ATTTACATGACTGAA[C/T]TAATTATTCCAAAAA | 11124 |
rs368358632 | snp | A/G | | | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462148 | GGACTTTGCCCATGT[A/G]CCTTTTCTCCTTGCT | 11124 |
rs368364556 | in-del | -/AGCC | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50846501 | GGCTTTAATCCTGAA[-/AGCC]ATGCCGCGGCCAGAC | 11124 |
rs368366543 | snp | A/G | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960502 | CCTCCCCCTAGCTGA[A/G]GCGGGGACCAGATTG | 11124 |
rs368370928 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649354 | TGGGGTTTCTCCATG[C/T]TGGTCAGGATGGTCT | 11124 |
rs368373234 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50474204 | CTCAAAAAATCAGAT[C/T]CCTCTTTTACAAGGC | 11124 |
rs368393172 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648819 | TAATCCCAGCTACTC[G/T]GGAAGCTGAGGTAGG | 11124 |
rs368395968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50885654 | GCCACTGTCTTTCCA[C/T]TGAAGAGTTTAGTCC | 11124 |
rs368401230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50731664 | TGAGCCACCGCGCCC[A/G]GCCTCAAAACACTTG | 11124 |
rs368407119 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50831805 | TATCCTTATCAGAGA[A/C]AAAAAAAAAAAAAAA | 11124 |
rs368415637 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50841582 | AGCTTTTTTTTCCCT[C/T]TCTTTCTTTGCCTTT | 11124 |
rs368416915 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50565956 | ATCTGTTTTTGGCAC[C/T]GCTTTTCATCACCTT | 11124 |
rs368461482 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927337 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 11124 |
rs368461682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50802817 | CAAAAACAAAAAACA[C/T]CTACCAATTCAATGT | 11124 |
rs368463765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50630565 | TGCATAATTTTGTTT[G/T]CTTTCTTATTTTGTT | 11124 |
rs368465136 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50801426 | TAAAAGATGGTGTTA[C/G]CAAATATGCAATAAT | 11124 |
rs368467693 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50580190 | AATTATTTATATTTA[G/T]TTTATACTTGTTTGT | 11124 |
rs368482838 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760159 | AAATATATATGCACC[C/G/T]AATACAGGAGCACCC | 11124 |
rs368484521 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50456732 | GCTCTCAGGAGTATA[C/T]AGTCTAGGGCAGAAT | 11124 |
rs368487313 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50891229 | GTCATTTAAGGACTT[A/C]TCTACATTGGTTATT | 11124 |
rs368504398 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643741 | GGGATTACAAGCATG[C/T]ACCACCATGCCTGGC | 11124 |
rs368505105 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50859515 | CATTTACAATAGCCA[A/C]AAAGAAAATGAAATA | 11124 |
rs368506478 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50708438 | GTGGAGTAGTGGCAG[C/G]TGAGGTGGAGAAATT | 11124 |
rs368506601 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677794 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATC | 11124 |
rs368511303 | in-del | -/CCAGAC | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50910149 | TGCTGGAGGTCCACT[-/CCAGAC]CCAGACCCTGTTTGC | 11124 |
rs368513570 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50876602 | TTGTTTTGTTTTGTT[C/T]TGAGATGGAGTCTCA | 11124 |
rs368516806 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50659540 | ATTCCAGTTAAGGAC[A/G]AGTGGCACTTCACAG | 11124 |
rs368519292 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50607807 | GATAAACCTCATTTA[C/T]TCAGCTAGTTCCTAA | 11124 |
rs368530523 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50866981 | TCATGGTACTGGTAT[A/G]AAAATAGGCATATAG | 11124 |
rs368530740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626345 | CTTGTGGAACATATG[C/G]TATAAAATAGGAAAT | 11124 |
rs368541598 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50944320 | AATTTGGAGGAGCTG[C/T]ACCAGAGTGTTTTCT | 11124 |
rs368546564 | snp | C/T | 3.30611e-05 | 0.00406565 | intron-variant | FAF1 | GRCh38.p7 | 1:50801681 | ATTGATAGCTGCCTG[C/T]AAACAAGAAACAGAG | 11124 |
rs368546912 | in-del | -/T/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50617693 | GTCCCTCCTCTTCTG[-/T/TT]TTTTTTTTTTTTTTT | 11124 |
rs368566999 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50871228 | CAAGGAAGGAAGTCA[A/C/T]CTCCATAACATGAAA | 11124 |
rs368574629 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50632656 | GGGTAGTGTCTCCGA[C/T]TCTTCTTGACATTTT | 11124 |
rs368592978 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591468 | ACGACTTAAGGTCAG[C/G]AGTTACCAGCCTGGC | 11124 |
rs368595076 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50609037 | ACAGACAGACAGTAC[C/T]ATAAGTAGAGTGCAA | 11124 |
rs368598592 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50930758 | CAATGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 11124 |
rs368602663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50538828 | CTAGAGGTCTGGTTT[C/T]ATTTGGGTTTTAAAG | 11124 |
rs368624043 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50484150 | ATGGATCCCATATAG[A/G]GACAGTTGATTTGAC | 11124 |
rs368639195 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50530814 | CAAGAACAACAACAA[A/C]AAAAAACAAACTGCA | 11124 |
rs368642190 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50567592 | AGAGAAATATTAACT[G/T]TGAACTGTTCAACAA | 11124 |
rs368658522 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457198 | ATCTTCAGGTTTGGG[A/G]TTCAGCCAAACCTGA | 11124 |
rs368676714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50734676 | GGGGCGGAGCTTGCA[C/T]TGAGCCGAGATCACG | 11124 |
rs368683937 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50763100 | TCTCTACTAAAAATA[C/G]AAAAAAATTAGCTGG | 11124 |
rs368686034 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447259 | GCCTCCCGAGTAGCT[A/G]GGACTACAGGTGCCC | 11124 |
rs368691549 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50954090 | AGTAGCTGGGACTAC[A/G]GGTGCCCGCCACCAT | 11124 |
rs368694488 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556599 | CCAGCACTTTGGGAG[G/T]CTGAGGTGGACAGAT | 11124 |
rs368698264 | in-del | -/GC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50606488 | GTAGCTGTGAGAGTT[-/GC]TTTTTTTTTTTTTTT | 11124 |
rs368699919 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50472607 | GTTTTGGTTGGGGGC[A/G]GGTGGCAGGCATGGG | 11124 |
rs368715640 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50777421 | CAGCAAGACTCTGTC[A/C]CTTAAGAGAAAAAAA | 11124 |
rs368727888 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50496098 | CAGTAGTGTTAAAGA[C/T]TAGTAATCATCAGTT | 11124 |
rs368729685 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779983 | AAGCACACATGCACA[C/G]ACAGACAGACACACA | 11124 |
rs368741993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695057 | TGTAAAACAAAATTT[C/T]CTATTCATCTGAATA | 11124 |
rs368752897 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50480804 | GTATTTTTTAGAAAA[C/G]TTAACCATAAAACAG | 11124 |
rs368756215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50710665 | TGGAGTGCAGTGGTG[C/T]GACCTCGGCTCACTG | 11124 |
rs368764899 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50918174 | ACTGAATGTAAATTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs368768507 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750112 | CTGGAATGTAGCAAG[C/T]TTCAGAGCCAGAATT | 11124 |
rs368774025 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874754 | ATCTTATTTTCTTTT[C/T]TTTCTTTTTTTTTTT | 11124 |
rs368774715 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457766 | AAAATTATCCAGGCA[C/T]GGTGGTGTGCACTTA | 11124 |
rs368778606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739304 | TGTACATGTGTACAC[A/G]TACATGCATATACAT | 11124 |
rs368779032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908647 | TTCTTTGTCTCTTTT[A/G]ATCTTTGTTGGTTTA | 11124 |
rs368780164 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725981 | TAACTGGGGCCAGGC[A/G]CAGTGCCTCATGCCT | 11124 |
rs368781425 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50831750 | TAAGGATTGGGATTA[C/T]ATAATGTTGGATTAT | 11124 |
rs368788567 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50521892 | AGGGCTGGCTCTGAA[C/T]AGGTGTGCTGAATTG | 11124 |
rs368788700 | snp | C/T | 0.000945866 | 0.0217264 | intron-variant | FAF1 | GRCh38.p7 | 1:50705782 | GCTGTGAGACATAAC[C/T]CACCTCTTGAATAGT | 11124 |
rs368792194 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50760778 | TCACAATTAAAAGAA[C/T]TAGAAAAGCAAAAGC | 11124 |
rs368819328 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50489217 | CTTATAGGCAGAAAA[C/T]GTTTTATTATCCTTT | 11124 |
rs368823532 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50517938 | TTTTAAAGTCCATTA[A/C]ATAAACTTACTTTTC | 11124 |
rs368825062 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50534278 | TTGGGGTCTATATTA[A/C/T]CTTCTGCTGATAATT | 11124 |
rs368832083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50741853 | GTTCCATTTTAAACA[C/T]GTTAAGTTTGAGACA | 11124 |
rs368864403 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50595575 | TGAGATGCATTCTCA[G/T]GCTGTTGCTTAGGCT | 11124 |
rs368874754 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50548206 | TTTTTGTCTTTAGCA[C/T]AGTAAGAATATTTTG | 11124 |
rs368887594 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50860016 | AAAGGACTGCCTATT[G/T]AATAAACAAACAGTG | 11124 |
rs368898912 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50952441 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCGCT | 11124 |
rs368916245 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50784640 | AGATTCAATGCAATC[G/T]CTATCAAAAGCCCAA | 11124 |
rs368917749 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50765831 | CATGGTGACTCACAC[C/T]TGTAATCCCAGCACT | 11124 |
rs368923982 | in-del | -/AGA | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50720906 | ATCATACCATCCACC[-/AGA]AGCCCCACGCTCCTA | 11124 |
rs368927804 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50730751 | CTCCTGCCTAACAGA[A/C]TAGGCTCCACATTTT | 11124 |
rs368955607 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50565555 | GTCTCTGTAACCTGC[A/G]AACTCTTATTACTAG | 11124 |
rs368968065 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468274 | AATATAAAATTATTA[C/T]ATGACAATTAAAATT | 11124 |
rs368971716 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50671635 | TCCTTAATGTATTCA[C/T]GTAGTAGGTTAGCAG | 11124 |
rs368972971 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50811859 | AGCATGGTACTGATA[C/G]AAAAACACATAGACC | 11124 |
rs368974787 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50959776 | CTTCACCTGAAAATC[C/T]GCCAGGATCATCTCC | 11124 |
rs368980622 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50857461 | CTCGCCTTTTGATTA[C/T]TGCCAAAAAAGAAAA | 11124 |
rs368985787 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50713033 | CCAGCATGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 11124 |
rs368990818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888358 | TTTTCTTAATTGAAT[A/C]CCCTTTCTTTCTTTC | 11124 |
rs368993720 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50696088 | AGGAAATCATGGCAC[C/T]TTGATTTCTAACAAT | 11124 |
rs368994794 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875047 | TGTGAGAAAGTTATA[C/T]CACCATGTTTTTTAT | 11124 |
rs369006731 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50909064 | AGCTCTTGTAAGGTA[C/G]GCCTGGTGGTAACAA | 11124 |
rs369007203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768367 | TCAACACCCCACTGA[C/T]AGAATTAGATCACTG | 11124 |
rs369008229 | snp | A/G | 1.68937e-05 | 0.0029063 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50539680 | TTTTTGAGTCCGAAT[A/G]GTTTGTGCCACAACA | 11124 |
rs369009192 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50485789 | GAAGGATGACTGGGA[A/G]GCCTCAAGAAATTTA | 11124 |
rs369013289 | in-del | -/GAAA | 0.0640901 | 0.167145 | intron-variant | FAF1 | GRCh38.p7 | 1:50519327 | GAGCGAGACTGTCTC[-/GAAA]GAAAGAAAGGAAGGA | 11124 |
rs369013617 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50926649 | ATTTGATCACTACAC[A/G]TTGCATATTCTTATG | 11124 |
rs369015091 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50846292 | GCAAGTGACAAGCTG[G/T]CATCAGAAACAGACT | 11124 |
rs369015554 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545367 | GCAACCTCCGCCTCC[A/C/T]GAGTGATTCTCCTGC | 11124 |
rs369024705 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50700152 | CCTTTCATACCCCCC[C/T]TTTTTTTTTTATTTC | 11124 |
rs369049099 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819394 | TTGAGGAAGGGAGAT[C/T]GAGTGAGCCTAGGGG | 11124 |
rs369055144 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458977 | GCCCTTTTTTTTTTC[-/T]TTTTTTTTTTTTGAG | 11124 |
rs369076651 | snp | A/C/T | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50921237 | GACCGACCTGCCCCA[A/C/T]CTGCAGTAGCCAACA | 11124 |
rs369081361 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729060 | TATATATATATATAT[A/T]TTTTTTTTTTTTGAG | 11124 |
rs369085593 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50574756 | TTCTTACTGAAAATC[A/G]TAAGAATTACAATGA | 11124 |
rs369088622 | snp | C/T | 0.000184441 | 0.00960137 | intron-variant | FAF1 | GRCh38.p7 | 1:50539747 | AAAGGAGACAAAATA[C/T]AAAGTAAGTTTTGCT | 11124 |
rs369097063 | in-del | -/ATT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643938 | TTTATATATTTTATT[-/ATT]TCCTCTTATGTTTTC | 11124 |
rs369107993 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50452426 | GAACCTCAGAGCTGG[G/T]TTGCTTCTGACTCTG | 11124 |
rs369124654 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50666313 | GATCTCCTGGGCTGA[C/T]AAGATCCTCCCAACT | 11124 |
rs369141849 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50952260 | TTGCAGGCGCGCGCC[A/G]CCACGCCTGACTGGT | 11124 |
rs369142458 | in-del | -/AAGTCAATAAGAAAATGGGGGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50806195 | TAAGAAAATGGGGGA[-/AAGTCAATAAGAAAATGGGGGA]GACAGACACTTCTCA | 11124 |
rs369142765 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50806470 | CGGAGGCAGCCGACA[C/G]CAGTGGAAGCACATA | 11124 |
rs369151162 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640311 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 11124 |
rs369153028 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50859903 | ACAAAAACAGACATA[A/C]ACACTCATGGAACAG | 11124 |
rs369156147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460425 | AAGTGCTGTCTAGTG[G/T]TCCTAAGTAAAGGAG | 11124 |
rs369159324 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50842945 | CTTTGTCTTGTTCAC[C/T]GCCACATCCCCTGTG | 11124 |
rs369163228 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50520720 | AGGTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 11124 |
rs369165759 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50835303 | AGTAATCCAAACTGA[A/G]ACTTAAGCAATGGTA | 11124 |
rs369168116 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50798091 | AAAAAAAAAAACTCC[A/G]CATTTATTTTAGAGA | 11124 |
rs369170390 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510888 | AAGTATTGTTATTAG[C/T]CTATTTTTTAACTCA | 11124 |
rs369171368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50900596 | CTTCACCTCTCTATT[A/G]TCTACAGAGAAAAAT | 11124 |
rs369172958 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50680972 | TTACCTTAACAGATG[C/T]ATTTACATATACAAA | 11124 |
rs369174099 | in-del | -/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820482 | TACCTTTTGTGTGCA[-/TG]TGTGTGTGTGTCCAT | 11124 |
rs369191154 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50585279 | TGTGAAATATGGTAC[A/C/G]CTATCCTCACATTGT | 11124 |
rs369208892 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50674012 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 11124 |
rs369213493 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928655 | GAGCATGATGGCGGG[C/T]GCCTGTAATCCCAAC | 11124 |
rs369219552 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50534084 | CTTCCAGCTTCTAAT[A/T]AGGCTAAATTAATAG | 11124 |
rs369235865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50573827 | AAAAACAAAAAAAAA[A/C]AAAACAAAACAAAGC | 11124 |
rs369240400 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863252 | AAATTAAATAATCCG[C/T]TCCTGAATGATCTTT | 11124 |
rs369248360 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619572 | CCAAATCTCTTTTAG[C/T]TTGTAGGGTTTGTGC | 11124 |
rs369288416 | in-del | -/AC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779991 | TGCACAGACAGACAG[-/AC]ACACACACACACACA | 11124 |
rs369291254 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50560133 | AAGTGTAGGGTTAGA[A/G]TAACATGGTCAGCAA | 11124 |
rs369293143 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50732842 | TTGCTGATGTATTGA[A/C]TGAGTTCCTCATTCC | 11124 |
rs369303347 | in-del | -/CTCT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928183 | CTTTTACTGCATGCT[-/CTCT]GTCTTTGGCACACAG | 11124 |
rs369314024 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724767 | GAAGCCAGGGACAAG[A/G]CCAGCAGTTTCCTCT | 11124 |
rs369314423 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767860 | CACTTAAATACATAG[A/G]CCATTAGCCCTACAA | 11124 |
rs369327798 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735065 | GGTATCTAAGAATAT[A/T]TTCTATACAGGAATA | 11124 |
rs369341634 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783599 | AAAAAATCGGCCAGG[C/T]GCGGTGGTTCACGCC | 11124 |
rs369343137 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50582223 | CCTTCTAAGCACATC[C/T]ACCTTTTTTCCCATT | 11124 |
rs369350966 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50795776 | TCCACAACACTTCCA[C/T]TGAATTGGAACTTGA | 11124 |
rs369356394 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50522101 | ACAAAAGTAGAAGTA[C/T]GCAATTAAGAGAAAC | 11124 |
rs369359287 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50774183 | GTCTTTCTTCCCCCA[A/G]AATACAAGCTATAAT | 11124 |
rs369362514 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50496530 | TAGGTTATCCATCTT[A/G]ATAATCCAGAAGCCC | 11124 |
rs369370456 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50728765 | CACTGCACTCTAGCC[G/T]GGGCGACAGAGCCAG | 11124 |
rs369391408 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50937284 | CTTGATCTCTTCTTT[G/T]GAAGTGTTTCATTGA | 11124 |
rs369394861 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50632294 | GAGTTTAGCTTACAT[-/C]TATTCTAAATAAGAC | 11124 |
rs369419636 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50592864 | AATTGCTTGAACCCG[A/T]GGGGAGAAGGCTGCA | 11124 |
rs369427628 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50557835 | TTTTCAGACCTTTTT[A/C]ATTTCAGGCAAGAAG | 11124 |
rs369433481 | snp | C/T | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460287 | TGCTTGGCAAATGCC[C/T]ATTCCTTTCTTTCTG | 11124 |
rs369448455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50442546 | GGACACACAGATAAA[C/T]GGGCAACTCCAAGTG | 11124 |
rs369453261 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50651060 | GTTGACTTCACTGAG[A/G/T]AACCTGAAAATGCCC | 11124 |
rs369453465 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50911022 | AACCTCCTTTCACCT[C/T]CCTTTTTCTCCTAAG | 11124 |
rs369466762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581090 | AGTATTTTCCATAAA[C/T]CTATATTTATGAACA | 11124 |
rs369489788 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869732 | TATAGAGTTTTTTCT[C/T]TGAGGATGTACTTTT | 11124 |
rs369495877 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656512 | ACATGCAACATTATA[A/C]CTTTTACTTTGAAAG | 11124 |
rs369496662 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619216 | GTGTCTTTTAAGTGA[A/G]GCGTTTAGCCCATTT | 11124 |
rs369499234 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50730698 | CTATACCCAAATGGC[C/T]CAGGCCAGTGGTCAG | 11124 |
rs369508602 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731372 | GTTTTATCTTTTCTC[-/T]TTTTTTTTTTTTTTT | 11124 |
rs369510050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669910 | GCGGATCACTTGAGG[C/T]CGGGAGTTCGAGACC | 11124 |
rs369511155 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50682813 | TAAGATCTGAATATG[G/T]CCGGGCGTGGTGGCT | 11124 |
rs369511509 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50734860 | GTGAGTTGCTAAATA[C/G]AGATTTGTAAGTTAT | 11124 |
rs369529067 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50773099 | TTAAAATGCTTTAAC[A/G]TAACACCTACAATTA | 11124 |
rs369529286 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50784989 | ACATGCAAAAGAACT[G/T]GGAACCTCATAACCT | 11124 |
rs369543928 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662071 | CAGGGCTGGCCTGTG[C/T]TGGAGAATTCAAATC | 11124 |
rs369545258 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50815519 | GAATACTGCTGTGAT[G/T]AACACATTTTGGTAG | 11124 |
rs369556430 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50693431 | TCCACAGTCTTAATA[A/C/T]TCATATGGAATTTTA | 11124 |
rs369556486 | in-del | -/TCA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50913613 | AACAGCAGATAATTA[-/TCA]ATCAAAATAATGACA | 11124 |
rs369568153 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909915 | CATCCAGCTTTGTTC[C/T]GTTGCTGGTGAGGAG | 11124 |
rs369569714 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828275 | TTTTTTTTTTTTTTT[C/T]TTTCTTTTTTTGAGA | 11124 |
rs369572337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609810 | AAAAAAAAAAAAGTT[A/C]AGTCATTAGATTGCC | 11124 |
rs369588923 | in-del | -/CA | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50766657 | CACAGGGCTACCGTG[-/CA]CAGGTATTCATTCTT | 11124 |
rs369597338 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50497466 | AGGAATGGCTTTGTG[C/T]CTAGACAAGGGAATA | 11124 |
rs369598088 | snp | C/T | 0.279461 | 0.248258 | intron-variant | FAF1 | GRCh38.p7 | 1:50864353 | TTTAGTGCTATAAAT[C/T]TCCCTCTACACACTG | 11124 |
rs369603599 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50668224 | AAGTTTGGGAACAAC[C/T]AGGCCAGTGTTTGCA | 11124 |
rs369634001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560119 | GCCAGATCAAATGGA[A/C]GTGTAGGGTTAGAGT | 11124 |
rs369637464 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447148 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCCCTCTGT | 11124 |
rs369640415 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562946 | ACTGAACATGTACAC[C/T]TTTTCCTTGTCATTT | 11124 |
rs369640627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50525857 | TGTGAATGCAAAATA[C/T]CTGCATGTATATTTC | 11124 |
rs369651237 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469041 | AGATTAGAGTTTCAT[A/G]TATAGACCTATTTAA | 11124 |
rs369659984 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50691229 | CAACATCTTTGCCAA[C/T]ACAACACTTGTCACT | 11124 |
rs369676986 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50662526 | TCCTGAAACACTACC[C/T]AGCATAAGATTTAAC | 11124 |
rs369682545 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50906428 | AAGAAAGTCATTGGT[A/G]GCTTGATGGGGATGG | 11124 |
rs369690565 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50635249 | AAAGGAAGATAAAGG[A/C]ACATTTTTGCTTGTT | 11124 |
rs369691640 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50913788 | ACTGATGGATGAATA[C/T]CCAAACAGCAGAAAT | 11124 |
rs369695568 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50716547 | CTCTGTGTCTAGCTA[C/G]ACAATTGTAAATACA | 11124 |
rs369701510 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447286 | GCCCGCCACCACGCC[C/T]GGCTCATTTTTTGTA | 11124 |
rs369708828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50447226 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 11124 |
rs369712410 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50849266 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 11124 |
rs369730178 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50705090 | ATAGTCATCATTTCA[A/C]TGTTTCTAAACATAA | 11124 |
rs369730499 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50650893 | TTTCCTACTGGTAAA[A/G]CTTTAGATACCTATT | 11124 |
rs369742313 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929187 | AAATGATGTGTTTAA[A/T]AATACTCTCAAAGTA | 11124 |
rs369751522 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50710804 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 11124 |
rs369760816 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50832829 | CTCTAGTTATAAAGT[G/T]CCATTTCTTTGCATC | 11124 |
rs369774023 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FAF1 | GRCh38.p7 | 1:50739374 | TGTGTACACGTACAT[A/G]CATATACATATATGT | 11124 |
rs369774201 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466000 | AACTGATGGGGAGCT[A/G]TTACAGGGTTCGAAA | 11124 |
rs369775832 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713773 | GGCAAATGTAAAAGC[-/TT]TTTTTTTTTTTTTTT | 11124 |
rs369788654 | snp | A/G | 0.000221865 | 0.0105301 | intron-variant | FAF1 | GRCh38.p7 | 1:50452232 | ATAAAAGAAAGTCCC[A/G]CTTTACAGAACAATT | 11124 |
rs369794125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50951815 | GCAACATCACAAAAG[A/G]TATCTGTTTGGATCA | 11124 |
rs369805097 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50931730 | AACAACAAAAAAATT[A/C]GCCAGGCATAGAGGC | 11124 |
rs369806163 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50598335 | GGGCATGGTGGAACA[C/T]ACCCATAGTCCAGCT | 11124 |
rs369808758 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649708 | AGCACTTTGACAGGC[C/T]GAGGCAGGTGGATCA | 11124 |
rs369809246 | in-del | -/A | 0.160609 | 0.233472 | intron-variant | FAF1 | GRCh38.p7 | 1:50538111 | TCATTATAGGATATT[-/A]AAAAAAAAAAATCAC | 11124 |
rs369818345 | in-del | -/GATGGCTACCAAGCC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50509116 | GATGGCTACCAAGCC[-/GATGGCTACCAAGCC]AATGGCTAAACAACA | 11124 |
rs369823851 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50856506 | TATACAAATATTTGT[A/C]AATTTTGACAAGTAC | 11124 |
rs369827071 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789163 | TCATTAGCTCTACAC[C/T]AAGTATTATCCCTTT | 11124 |
rs369829891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50825408 | ATATTACAAAGTCCT[A/G]TGTAATACAAGACAT | 11124 |
rs369830715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50451595 | ATTCTAAGTCCCTTG[C/T]TTGGGAGGACTGTAC | 11124 |
rs369835896 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50799105 | GCGTGAGCTACCACG[C/T]CCAGCTCTCAAAGGA | 11124 |
rs369838098 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50549105 | CAGATCACTAAACAG[C/G]AAGTTATTCTTTACA | 11124 |
rs369842520 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556497 | CACTATACAGTTCAT[A/C]CATGTAACTAAAAAC | 11124 |
rs369842667 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50835523 | TTGCAGTGAGCCGAC[A/G]TTGCGCCACTGCACT | 11124 |
rs369843554 | snp | C/G | 0.000164959 | 0.00908033 | missense | FAF1 | GRCh38.p7 | 1:50596142 | CGACTGTTCCCGGGT[C/G]TGTGCAGGTGAAGAT | 11124 |
rs369844200 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50487999 | TAGGGTGCCATGATA[C/T]GTTAATTGTTGTTCC | 11124 |
rs369856631 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527548 | AATAATCACTAAGTG[A/T]AAAACTTCTGTAATA | 11124 |
rs369863216 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894371 | TGGTGAATGCTGTCA[A/G]GCCTGGGACTCTCTC | 11124 |
rs369870162 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50490270 | GAGGCTGAGGCAGGA[A/G]AATCACTTGAACCTG | 11124 |
rs369877703 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648782 | AAATATAAAATCAGC[A/C/T]GGGTGTGGTGGCGCA | 11124 |
rs369878989 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50590567 | TTTGGAGTTGTCTAC[A/C]TATAAAATTATCCTC | 11124 |
rs369891385 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543474 | AAGAGCCTCAGGTAT[A/G]AAGTGGAAATAACAC | 11124 |
rs369913122 | snp | A/G | 1.70731e-05 | 0.00292169 | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959846 | GGCTCCGGGAGCGAA[A/G]CGCGCACCTGGGAGG | 11124 |
rs369942624 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | FAF1 | GRCh38.p7 | 1:50567028 | GATAAACACAATGAT[A/T]TTTTTTTTAATAGAA | 11124 |
rs369951593 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808937 | TCAACAAGAAGACCT[A/G]ACTATCCTAAATATA | 11124 |
rs369960248 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475506 | CTTGTACTCATCCCA[C/T]GGAAATCCTTTGGAA | 11124 |
rs369963161 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729649 | CAATCTCAGGTGATC[C/T]GCCTGCGTTGGCCTC | 11124 |
rs369971124 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767088 | CAATAAAATGATTTG[A/G]GAGATGAAAAATGAA | 11124 |
rs369973542 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50695416 | CCACCTTGGATAGAC[A/G]TCCACTGTATTAACA | 11124 |
rs369995683 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750785 | ATCCCACCACACTCA[A/G]CTAATTTTTGTATTT | 11124 |
rs369997224 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50944548 | CACCCAGACCTTTCA[G/T]CTGGAAATGTCAGGC | 11124 |
rs370005087 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447848 | ACCCTCTCCTCTCTG[A/G]ATTCCTCTGTGCTGA | 11124 |
rs370005460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50828560 | AGGCCTGAGCCACCG[C/T]GCCCGGCCAAGAAGG | 11124 |
rs370012962 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50843976 | TTTCCATAATGGCTG[G/T]ACTAATTTACATTCC | 11124 |
rs370015986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50747909 | TGGCAATGTGACGAT[A/G]TCTGCTCCTGCTTTG | 11124 |
rs370024274 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50833886 | CTCCTTTTCCAAATA[C/T]TGATCACATTCCAGG | 11124 |
rs370024425 | snp | A/G/T | 0.000152558 | 0.00873254 | missense | FAF1 | GRCh38.p7 | 1:50539663 | AGCGGAAACTGATCC[A/G/T]TTTTTTGAGTCCGAA | 11124 |
rs370027811 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687497 | GCTCATGCCTGTAAT[A/T]CCAGCACTTTGGGAG | 11124 |
rs370028338 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50502984 | GTGCACCACCATGTC[A/C]GGCTAATTATTCTAA | 11124 |
rs370031236 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50559506 | TTTGAAACCCTACAC[C/T]AATAAAGTCATTAGA | 11124 |
rs370032041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497784 | TGAACTCCTGGGCTC[A/G]TGATCCACCTGCCTC | 11124 |
rs370034050 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50764684 | GTTGTTTCATATATT[G/T]TCTCCAGCTTTCCAG | 11124 |
rs370036058 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725486 | TTTGAGACAGAGTCT[C/G]GCTCTGTTGCCCAGG | 11124 |
rs370038178 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50804094 | TATCAATTGTTCATA[C/T]AATAAATGTGTATTA | 11124 |
rs370047068 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50860090 | CCCTACTTTTCACCA[C/T]ACACAAAAATTAACT | 11124 |
rs370056145 | snp | G/T | 0.000164978 | 0.00908086 | missense | FAF1 | GRCh38.p7 | 1:50744764 | CATTTTCTAGAATCT[G/T]TTTAATCTCTCCTGT | 11124 |
rs370058802 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FAF1 | GRCh38.p7 | 1:50918603 | ATCATTGTTGGACAT[C/T]TGGGTTGGTTCCAAG | 11124 |
rs370070091 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958519 | TGTCTCTACTAAAAA[C/T]ACAAAAATATTAGCC | 11124 |
rs370074577 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638801 | AATTCTTCTCTATTC[C/T]CAGTTTGCTAAGTTA | 11124 |
rs370078605 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50861565 | TGTGGCAGGGTAGGA[C/G]GTAGTAAGGGACAAA | 11124 |
rs370084115 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50603005 | TTAGAGATGAGGTTA[C/T]TAAATCTCACACAGA | 11124 |
rs370086564 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50879737 | GAACATGTTTGAAAT[A/G]TAAATTCTCAGGCCT | 11124 |
rs370092938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50919324 | CTGCTAATCTACACA[A/G]AGAGCATCAGAAATA | 11124 |
rs370098443 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50647389 | TCGCTTCTTTCTGTA[A/C]GTCACTTTCCTTTTT | 11124 |
rs370103366 | snp | C/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50866101 | TAAAAACAAACATCA[C/G/T]ATGATAATCTCAATA | 11124 |
rs370129708 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787140 | AACATAGTTAAACTA[C/T]AGTAACTTGGTAAAG | 11124 |
rs370146036 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50741092 | AGGCTTTAAATATAC[A/G]ATGATGAAAGAAACA | 11124 |
rs370152291 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50688090 | CAGGGAGCCGAGATC[A/G]CACCCACTGCACTCC | 11124 |
rs370152651 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50551856 | CTTTGTCCTGTTAAC[A/G]TTTTCATAAATATCT | 11124 |
rs370154209 | in-del | -/T | 0.460702 | 0.134554 | intron-variant | FAF1 | GRCh38.p7 | 1:50672019 | CCAGGGTGGTCTTTC[-/T]TTTTTTTTTTTTTTA | 11124 |
rs370155018 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830658 | TCCTCCAGTGCTCAA[-/T]TTTTTTTTTTTTTTT | 11124 |
rs370168274 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50695735 | TCACTTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 11124 |
rs370172108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50718112 | GCAACCTCCGCCTCC[C/T]GAGTTCAAGCGATTC | 11124 |
rs370172853 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950536 | GGGTATGGCTGTGTT[A/G]CAATAAATCCTTATT | 11124 |
rs370197200 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50741983 | TAATGTCATGGGAAT[A/G]GCAGAAATCACCTAG | 11124 |
rs370203778 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50517608 | AACAAGCTCCCCAGG[C/T]GATTGTGATACTAGT | 11124 |
rs370213986 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50492138 | AATAATATACAAACT[A/G]TCTAGCAAAGGACCT | 11124 |
rs370221661 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50473462 | AAACTTAGCTCCTAA[C/G]TTTTTTAAGTTCTCT | 11124 |
rs370241176 | in-del | -/GTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50736879 | CATGGATTTTGTTTT[-/GTTTT]TTAAATTGTCTCCCA | 11124 |
rs370246808 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50821461 | CATACCATTCTTATT[G/T]CCCATGGGCCCTTTA | 11124 |
rs370253911 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50516999 | CTTTGTATTTACATA[C/T]CATTATTCTAGTATA | 11124 |
rs370277376 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50480510 | ACTGAGCATCTTCTA[C/T]GAGTCAGGCATTGTT | 11124 |
rs370288194 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50889655 | AGCAGGTTGTTCAGT[C/T]TCCATGTAGTTGAGC | 11124 |
rs370292772 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | FAF1 | GRCh38.p7 | 1:50491692 | GAACAATTGAGTTCT[G/T]TATCCCAGAAGTACT | 11124 |
rs370311312 | in-del | -/TTTTTTTTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50497541 | TATTATTCAAAACTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 11124 |
rs370325543 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50657424 | ACTTGAGGCCAGGCA[C/T]GGTGTCTCATGCCTG | 11124 |
rs370340368 | snp | A/G | 9.99101e-05 | 0.00706718 | intron-variant | FAF1 | GRCh38.p7 | 1:50583619 | GTAGCATAAAACAGC[A/G]TCAAATTTATATAGT | 11124 |
rs370341819 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50930434 | TCAAATGCAGTTTTA[C/T]CATTTAACTAGCCCT | 11124 |
rs370356406 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707508 | GTTCGAGACCACCCC[A/G]GGTAACATGGTGAAA | 11124 |
rs370358206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50676781 | GAGCCAAGATCCTGC[C/T]ACTGCACTCTAGCCT | 11124 |
rs370358723 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50791220 | GAAATCCAAAGTGAG[C/T]TCTTAAATATCTATG | 11124 |
rs370370327 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701968 | TTCATCATGCTTCTT[C/G]TTGTAACAGATAAGT | 11124 |
rs370381814 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468227 | CAACAACAACAACAA[C/T]AACAAAACTGCATCA | 11124 |
rs370388751 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50587251 | TTCTCCATGTGTCTC[C/T]ATTATTCGTTTTCCC | 11124 |
rs370392778 | in-del | A/CC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576637 | ATCTCCGCACCGCCC[A/CC]CCCCCGCCACCACCC | 11124 |
rs370395022 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50897235 | TAGATGTCATCTATG[A/T]ATAACTCCCCTCATA | 11124 |
rs370402004 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50883750 | AAATTTTTTCAGCAT[A/C]ACTAGGAAATTTTCA | 11124 |
rs370422127 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50930343 | AAGTTTAGGGTACAG[-/T]TACTATTCAGGAAGG | 11124 |
rs370423156 | in-del | -/GGGTTCTGCATCTGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562866 | GGGTTCTGCATCTGT[-/GGGTTCTGCATCTGT]TGATTCAACTAGCCA | 11124 |
rs370425675 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50523706 | GCAAATATTTTCTTC[C/T]ATTCTGTGGGTTATC | 11124 |
rs370428653 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800729 | GCAGTTCATGGTGAA[C/T]TTCCTGATGTTTCTG | 11124 |
rs370437961 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820786 | TCACTTAGCATAATG[C/T]CTTCCAGCTTCTTCC | 11124 |
rs370446101 | in-del | -/TGTGGC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742392 | ATTTGGGAGGGGGGG[-/TGTGGC]GGGGGAGAGAGACTC | 11124 |
rs370452298 | snp | C/G/T | 0.000329791 | 0.0128371 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788113 | GATGGCATTACAGGT[C/G/T]GAAACGCTGAAGAAG | 11124 |
rs370467557 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50535265 | GAAATGCATCTTCAT[C/T]ATCCTTATTTATCGA | 11124 |
rs370471305 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545167 | CAAACTAGTAAGTAA[A/G]AGATCAACAAAAAAT | 11124 |
rs370478039 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562061 | ACCCTGACTGAGGCA[A/G]GAGAAGGATGGGGAG | 11124 |
rs370481238 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50742153 | GTCTCTACAAAAATT[A/T]AAAAAAAAAAAAAAT | 11124 |
rs370481737 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463581 | TTAATATCTCTTAGC[C/T]CCAGTTGTCTAACCT | 11124 |
rs370501994 | in-del | -/GG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917593 | AAAGGAAAGGAAAAG[-/GG]AAAGGAAAAAGGAAA | 11124 |
rs370537811 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50546242 | TGTAGCCATTAAATA[G/T]ATTTCTTTATTAACT | 11124 |
rs370545413 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50943873 | CACACATGGTACATC[A/G]GAAAAGAGAGGGTTG | 11124 |
rs370578254 | in-del | -/ATTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50564951 | TAGCTATGTAATTTT[-/ATTT]GTTTTTTTTTTATTA | 11124 |
rs370580221 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50521783 | CAATTGTGTTCTGTC[A/T]TTACATGGCAACTCC | 11124 |
rs370590053 | snp | A/G | 6.73548e-05 | 0.00580283 | intron-variant | FAF1 | GRCh38.p7 | 1:50655547 | TGAAAAGAAAGAAAC[A/G]GGACAATTAAAATAG | 11124 |
rs370601388 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50734078 | TTGGGAATACAGGCG[C/T]GAGCCACTGCACTCA | 11124 |
rs370614231 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50697632 | AAATTAAACAATGCC[A/G]GCTTTGCAATGAGCA | 11124 |
rs370615738 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800081 | CAACAAAATCCTACT[C/T]TGATCACAGTTCAAC | 11124 |
rs370625145 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50886737 | GGCTGCATAGTATTC[A/C]ATGGTGTATATGTGC | 11124 |
rs370628357 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50536476 | GACCAAACATTCTTG[C/G]TGGCATTTTTCCAGA | 11124 |
rs370641491 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472196 | GGAGTAGTGGGGTGA[A/G]TGTCATTACTCAGCT | 11124 |
rs370646020 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50495755 | GTTCCCTTTTCTCCA[A/C]ATCCTCTCCAGCATT | 11124 |
rs370646793 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50604656 | GAGTCTGCAGGTGCA[C/T]GCTGCCATGCCCAGC | 11124 |
rs370658999 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50916360 | AAAGGAATCCAAGGC[C/T]ACCTGACCCCAATAC | 11124 |
rs370676784 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50479851 | ACAATGAAGAGATAC[A/G]AGGTAAATCAGCAAC | 11124 |
rs370687801 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50892376 | TGTCCGACAAGCCCC[A/C]GTGAGATGAACCTGG | 11124 |
rs370692665 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50609069 | ATACCATTATCCACT[C/G]ACTTAACTAATAGTT | 11124 |
rs370693177 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641092 | CTGCCTCAGCCTCCT[A/G]AAGTGCTGGGATTAC | 11124 |
rs370706041 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50443373 | GGCTTTCTTCAGTCA[C/G]TTTGAGTGGGAGAGC | 11124 |
rs370722446 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50763738 | TATCACATAATGTAT[C/T]GACATTTTGTTAATA | 11124 |
rs370730696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50783402 | AAGAAGCTATCAGAC[A/G]AAAAGAAAACTACAG | 11124 |
rs370737565 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907715 | GCATTTCTGTGGGAT[C/T]GGTGGTGATATCCCC | 11124 |
rs370759273 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50920301 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs370768728 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50473447 | AGGGTTGGGAAGGGC[A/G]AACTTAGCTCCTAAG | 11124 |
rs370774322 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50661305 | TTTGCCAGAACGCTA[C/T]TGTGATATAGTTTTC | 11124 |
rs370782061 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50770431 | TACAAAATCAATGTA[C/G]GAAAATCAGTACCAT | 11124 |
rs370787457 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50948423 | TGGTGTAAGGCAAAG[C/T]GGGAGACAGCCTCTC | 11124 |
rs370791459 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50694021 | TATACATGACATATA[C/T]GACATATATATGACA | 11124 |
rs370797127 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725570 | AAGCAATTCCCGTGC[C/G]TCAGCTATACGAGTA | 11124 |
rs370800267 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812708 | TACCATTCGACCCCA[C/G]CATCATTACTGCGTA | 11124 |
rs370825624 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50873118 | TACTTGCTGAAGGCT[C/G]AGGTGATAATTAGCA | 11124 |
rs370825846 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50570702 | AACAAAAAATTTTCT[C/G]CTGCTTTTATAACAA | 11124 |
rs370829670 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50576259 | TCATCATGTTTTTTC[C/T]ATATTAGACATAGGC | 11124 |
rs370836990 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50543867 | AATTTTAAACATTTA[C/G]AACTGGATACAAAAC | 11124 |
rs370840376 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561844 | AGACGGATGGACGGA[A/T]GGACGGAAGGAAGGA | 11124 |
rs370848815 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929098 | AAAAAAAGAAAGAAA[A/G]GAAAAAAAAACTGGG | 11124 |
rs370854828 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50531486 | TTTGGAATCAGGCTT[C/T]AGGCAAAAATAGATT | 11124 |
rs370859036 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50852720 | GTTTACTTAACTTCA[C/T]TAGCCCTCAGTTTCT | 11124 |
rs370868444 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FAF1 | GRCh38.p7 | 1:50761735 | ACAACCAATATCATA[C/T]TGAATGGGCAAAAAC | 11124 |
rs370871766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625803 | TTAGACATTATCTTG[C/T]AGGCAACGGGAAACC | 11124 |
rs370879606 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863012 | ACCCTAGAACAAATG[C/G]ACTTAACAGACATTT | 11124 |
rs370899750 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50706066 | TGAGAACAACCAAGG[A/G]GAGCTAACCTGTTAA | 11124 |
rs370926574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50652861 | TAATTATAATGTCGA[C/T]TCATTTACTGAGTGT | 11124 |
rs370937786 | in-del | -/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468459 | ACTACACTTGGCTAA[-/T]TTTTTTTTTTTTTTT | 11124 |
rs370960423 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714338 | TGAAATCGTGTCTCT[A/T]CTAAAAATTAAAAAA | 11124 |
rs370961631 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679637 | ATTTAGAGATCATCT[C/T]TCATTCCCCTGAATC | 11124 |
rs370965451 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50698387 | ACTGAAAAAGAAAAA[A/C]CTCTTCTTCATGCAT | 11124 |
rs370969315 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50493175 | GTAGCTGGGATTACA[C/T]GCACCCGACATCACG | 11124 |
rs370976302 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50825574 | ACTCCATAATCATAG[C/G]GGAGATTTTAACGTA | 11124 |
rs370981028 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50743839 | GCACTTTGGAAGGCC[A/G]AGGCAGGTGGATCAC | 11124 |
rs370982938 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50801141 | ACACTGGATACTTCA[A/G]GTAAAATAGTTCAGT | 11124 |
rs370988022 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836876 | AATATTGACTCTATA[C/T]TGCAACTACAAAATA | 11124 |
rs370991877 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875497 | TTACTCTGTTGCCCA[C/G]GCTGGAGTGCAGTGG | 11124 |
rs370993874 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819841 | TATACCAGCTATTGT[A/G]TATCAGCTTCAGCAC | 11124 |
rs370995359 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643340 | CATTCTGGTTTTTTT[C/T]TTGTGTGCTACTGTT | 11124 |
rs370996440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50575268 | GAAATAATTTTAATA[C/T]GGGCACTAAAGATTT | 11124 |
rs370998026 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50452402 | CTTCTCAACTCTTGG[G/T]GCAGCCAGGAACCTC | 11124 |
rs370999702 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50848304 | CATGACAAAAATAAT[A/G]CCAAAAAAGTGCGAG | 11124 |
rs371008493 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50892366 | CTGCACCCACTGTCC[A/G]ACAAGCCCCAGTGAG | 11124 |
rs371010849 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50903758 | ACTAATTAGCAAAGA[A/T]CTGAATTATCCCTGG | 11124 |
rs371016015 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493034 | TAAAGGATTAAACTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs371022639 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50509842 | GCAAGTTCCTTGACC[A/G]CTTCCAACACTGATC | 11124 |
rs371039013 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812444 | TTTTCAAAAGAAGAC[A/G]TACATGCAGCCAGAA | 11124 |
rs371048459 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50841243 | CCCTTGACACATATA[C/T]ATAAAATTTTGTCTT | 11124 |
rs371056282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50565436 | AAAGCCTTAAACAAC[A/G]CCTTTATTTAGTGTT | 11124 |
rs371060021 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50594403 | ACTTTTGAAGTCTTG[A/C/G]TGATGACTTTTCCTA | 11124 |
rs371083173 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881295 | TAGGTGGCCCCCTTA[C/T]ACAATCTACTGAACT | 11124 |
rs371097004 | snp | C/T | 0.127944 | 0.218179 | intron-variant | FAF1 | GRCh38.p7 | 1:50762369 | GGAACCAAAAAAGAG[C/T]CTGCATCGCCAAGTC | 11124 |
rs371133021 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50720345 | TTTAAAAATCTAACA[A/G]TGATGCTCACTACAA | 11124 |
rs371135633 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50791321 | AGAAAAAGCTAGTCA[C/T]TGACTTACTGTTTTT | 11124 |
rs371155699 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746634 | AAGGGAAGCAGAGTG[C/T]AAAAGTTTGAAAAAT | 11124 |
rs371177591 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50657415 | TATGTTAAGACTTGA[G/T]GCCAGGCATGGTGTC | 11124 |
rs371182282 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50934444 | TAACACTGTCTTGGC[C/T]AGGTATGGTGGCTCA | 11124 |
rs371190715 | snp | A/G/T | 6.63178e-05 | 0.00575805 | missense | FAF1 | GRCh38.p7 | 1:50567116 | AGATCCCAAGCCCAG[A/G/T]TTATAAAATTTTGAC | 11124 |
rs371191897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688688 | GTTGTGGCGCATGCC[C/T]GTAATCCCAGTTACT | 11124 |
rs371199037 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50753725 | CACAGGTAATACAGT[C/T]AATAATAACTGCTCT | 11124 |
rs371205901 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50792793 | GGGGAGATGACACGA[C/T]TGAGAAAGACTCCTG | 11124 |
rs371207630 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50509633 | TAAATATCAAAAAAG[C/G]AAAAGAAGTGCCTGG | 11124 |
rs371220874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457517 | AAGCAACTAGAATAC[A/G]GAGCACAGAACTAAC | 11124 |
rs371223595 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779670 | ACAAAAAAACGTTTG[C/G]GGGTGGAGGGAAGTA | 11124 |
rs371256847 | in-del | -/CT | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50853496 | AGACAAATATAAGCA[-/CT]CTGAATAGAGTCTTT | 11124 |
rs371256903 | snp | C/T | 3.29674e-05 | 0.00405988 | intron-variant | FAF1 | GRCh38.p7 | 1:50655420 | AGGAGGATATAAAAC[C/T]GAAAATTTGACTGTC | 11124 |
rs371260813 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638354 | ATTGAATAGAACTTG[C/T]GCAAGTGAACATCCT | 11124 |
rs371264389 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750622 | TATCCTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs371286169 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960121 | GGGCCAGGATGAGGG[C/G]AGGTTGCGACAGCGC | 11124 |
rs371296122 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50456108 | TTTTTTTAGAGATGA[G/T]ATTTCACTATGTTGC | 11124 |
rs371299976 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683475 | GAGGTTGCAGTGAGC[C/T]GAAATCGCGCCACTG | 11124 |
rs371302373 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50921226 | CAGGGCCTAGGGACC[A/G]ACCTGCCCCACCTGC | 11124 |
rs371307118 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | FAF1 | GRCh38.p7 | 1:50738854 | TCCCAGGAAATATAA[A/G]CAACTTACCCAGCAT | 11124 |
rs371307386 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50668442 | GCTTTCAGCATTACT[C/G]TCAGAGATTTGTAGG | 11124 |
rs371309378 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679160 | TTAACACACAGTACA[C/T]TGTTTTGTAACTGCT | 11124 |
rs371330134 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | FAF1 | GRCh38.p7 | 1:50584714 | CTCAAGGCAGATGAC[A/G]CCATGCCAAATACTT | 11124 |
rs371333219 | in-del | -/AAC | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50852897 | GTTGTCAGGTTAAAA[-/AAC]AGAGAAATTGAAAAA | 11124 |
rs371339142 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50645706 | CACCTGCCTGTAGTC[C/T]CAGCTACTCTACTCG | 11124 |
rs371353477 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704176 | ATATAAGAGAAGCTA[A/C]TTTGAAAACACTGAA | 11124 |
rs371363016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50592676 | TTGTTGGCTGGGCAC[A/G]GTGACTCACACCTGT | 11124 |
rs371365074 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50660841 | GTTACTGTGGGAAAA[C/T]TGGTGGAGCCATTCT | 11124 |
rs371377671 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50663698 | GTGAGCCACCGCGCC[C/T]GGCCAGAAGCACCGC | 11124 |
rs371393939 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50957347 | CGAAATTTTCATTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs371395514 | in-del | -/AA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713155 | CAGAGCCAGACCCTC[-/AA]AAAAAAAAAAAAAAA | 11124 |
rs371396615 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50539958 | CTGTCTGGGGCTGAC[A/G]GCATAGGATTCTTTT | 11124 |
rs371410899 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808278 | GCTAAATATGGAAAA[A/G]AAAGACTAATACAGG | 11124 |
rs371420781 | snp | A/G | 0.00154611 | 0.0277609 | intron-variant | FAF1 | GRCh38.p7 | 1:50452078 | GGGGAGGAAAAAACC[A/G]TCTTAGTCTAAAAAC | 11124 |
rs371423654 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503296 | TTAACTGTATCTTAT[A/G]TAAATTCCATTTCCA | 11124 |
rs371424435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50771600 | TCAGAATGGCTATTA[C/T]TAAAAACAAAAAATA | 11124 |
rs371426770 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769788 | GGGTGTGGTGGCTCA[C/T]GTCTATGATCCCAGC | 11124 |
rs371430733 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50566937 | CTGCATGTGTTAGCT[A/G]CAACGAGCAGCTTTT | 11124 |
rs371440328 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50794000 | CTCAACCAACCAGTA[C/T]GTATAATGCAAATAT | 11124 |
rs371447975 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561526 | ATCAATATAGTACTT[A/G]CTCTTTAAAAGGTAG | 11124 |
rs371457258 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50552506 | ACAAAAGTGGAAAAG[A/G]TTGATATAACTCTTA | 11124 |
rs371474636 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50870788 | CCCTATTCTCTCAGA[C/T]ACAATATTGAAACGA | 11124 |
rs371476890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50447051 | TCATTCCATGAGTTA[C/T]AGGCTTTAGGTTCAA | 11124 |
rs371483175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609779 | ATGCAGGAACATGGT[A/G]AAGTTGAATTATGGA | 11124 |
rs371489890 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50889675 | TGTAGTTGAGCAGTT[A/T]TGAGTGAGTTTCTTA | 11124 |
rs371491003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855240 | AAGTTAGAGACTACA[C/T]CTTGTTATATTTTTT | 11124 |
rs371495112 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50578413 | AATTTTAAAAAATAA[A/T]CTTGAGCAAAATCTG | 11124 |
rs371502518 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50864040 | TATTTCTGTGGGATC[A/G]GTGGTGATATCCCCT | 11124 |
rs371504022 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640323 | TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG | 11124 |
rs371505670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50914771 | TATCCCTTCTATCTC[A/G]CTATCAAAGTAATGT | 11124 |
rs371506752 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50562522 | AGGAATGCTACTATG[G/T]TAATATAAAAATCTC | 11124 |
rs371521906 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465903 | ACAAATAGCAAAGAT[A/G]CCAAGGTAAATGGAA | 11124 |
rs371527815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50474325 | TCCCTCACCTTCCTA[C/T]CAGCCCTGCTCCAGA | 11124 |
rs371528456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50875548 | ACCTCCCTCTCCCAG[A/G]TTCAAGCAATTCTCC | 11124 |
rs371542925 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50891763 | TGAGGTGTCAGTCTG[-/C]CCCTACTGGGGCCTA | 11124 |
rs371553609 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951237 | AGACCCTGTCTCAAA[C/T]GAACAAACAAACAAA | 11124 |
rs371558804 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50849108 | TAAAAATACACACAC[-/A]AAAAAAAAATTATCC | 11124 |
rs371601966 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929282 | TACAATTTATACATA[G/T]GAAAGCAGAAGGAGT | 11124 |
rs371617118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50689311 | ATGTCCAGGCCAGGC[A/G]CAGTGGCTCACGCCT | 11124 |
rs371633650 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945200 | CTGTTAGACTGCAAA[A/C]AGTCCAGAAAGCCAA | 11124 |
rs371636601 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50764800 | ACTGCCAAGAAAAAT[A/T]TCAATGTTTTCTCAG | 11124 |
rs371636618 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50550718 | CTTTTACAGGGGATT[C/T]ATATTTTAAAAAACT | 11124 |
rs371637922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50739130 | CTTATTGCCCATATA[C/T]ATAATATATACATAT | 11124 |
rs371640599 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50592118 | CCCCCATTATCTATG[C/T]TCCCCTAGCATCTCA | 11124 |
rs371642589 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602881 | AGTTGTATAATAACT[A/G]CTACTATTAAGAGCT | 11124 |
rs371650861 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50807925 | AACCCCTGCAAGGTA[C/T]TATAAAAGACGACCT | 11124 |
rs371650931 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909022 | CAGTATTGGTTGTTC[C/T]TTTCCACGTTTAGTG | 11124 |
rs371653028 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50571617 | TTTTCCTACTGGCAA[C/T]AGTGTCTGGGATGCT | 11124 |
rs371653732 | snp | C/G | 1.70443e-05 | 0.00291923 | intron-variant | FAF1 | GRCh38.p7 | 1:50787987 | GAAGGCTTTATGGCA[C/G]GAAAAACCTTACCAA | 11124 |
rs371655188 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50518856 | TGCCATGAAACTGTT[C/T]ATCAGAGTGGCTGAA | 11124 |
rs371661726 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50495969 | TTGAATTTTATTACA[A/G]TTCACTGAAAATGAT | 11124 |
rs371682639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50729176 | TTCTCCTGCCTCAGC[C/T]TCCCAAATAGCCGGG | 11124 |
rs371685044 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50918174 | ACTGAATGTAAATTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs371685811 | in-del | -/CA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50903142 | CCCCAGTGCACAACA[-/CA]GATACCTGTTCATAT | 11124 |
rs371687957 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50488885 | TATTTTCTACCTTCC[A/G]TTATTGACAGTCCTC | 11124 |
rs371693133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50614826 | CCTGGGCCGCAACAG[C/T]GAAACTCCGTCTCAA | 11124 |
rs371697580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50813436 | AAATGAGATCTTACT[A/G]TATGTGCTATTTTAT | 11124 |
rs371701846 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50547986 | AGACTCTTAGGAGGG[A/G]TAATAGAGAACATCT | 11124 |
rs371710489 | in-del | -/AGATAAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50581625 | AAGTGTAACAATAAG[-/AGATAAG]CAGAGGGTTTTTCAC | 11124 |
rs371721063 | in-del | -/AAAAAAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694793 | TCTACTAAAAAATAC[-/AAAAAAA]AAAAAAAAAAAAAAT | 11124 |
rs371738517 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50547456 | TTTGCTCTTGTTGCC[C/T]AGGCTGTAGTGCAAC | 11124 |
rs371740817 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803723 | GAGGGGATTCTATAC[A/G]GAAGGAACAGTGATA | 11124 |
rs371753767 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622164 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAATA | 11124 |
rs371753781 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940173 | CACTTCGGCACCCCA[A/C]GGTGCTGGGATTACA | 11124 |
rs371756311 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648702 | GAAGCCGAGGTAGGC[A/G]GATCACCTGAGGTAG | 11124 |
rs371757045 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50572587 | CAAGATAAGTGCAAT[C/G]TGAGAACACAAGCAG | 11124 |
rs371758088 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820867 | TGTGTGTGTGTGTGT[A/G]CACATACCAGATTTT | 11124 |
rs371773045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50597439 | GTGGTGATGATGATG[C/T]TTATATATAAAAAAA | 11124 |
rs371780890 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50795424 | AAGGAACTTGTTTCA[C/T]AGCAAAAGAAGTGCA | 11124 |
rs371808414 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50816204 | TTTTTTTTTCCTTTT[C/T]CTTTTTTTTTTTTTT | 11124 |
rs371814689 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50751601 | CCCACCTCAGCCTCC[C/T]AAAGTGCTGGGATTA | 11124 |
rs371817682 | snp | C/T | 6.6201e-05 | 0.00575292 | intron-variant | FAF1 | GRCh38.p7 | 1:50801718 | ATTTAAAGAAACAGA[C/T]AAATGCCCAAGTGTG | 11124 |
rs371821832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50687996 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT | 11124 |
rs371839622 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50701410 | TTAAAGTATTGGGTG[-/T]TTTTTTTTGGTTTGT | 11124 |
rs371847916 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50478147 | TGGGATCATCTATTT[C/T]TCAGTTACAGTGGTG | 11124 |
rs371848278 | snp | A/C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50784294 | ACACTAAGGATTCTA[A/C/T]CAAAGAAAAAAAAAA | 11124 |
rs371866360 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50802791 | GTATCCACATCAAAA[C/T]GAATAACCCACAAAA | 11124 |
rs371875581 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50558873 | CTGTAGTACTAGGTA[A/G]GAGTGTAGGAAGTAT | 11124 |
rs371878564 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50740043 | CAACAGATATTTTTT[-/T]GAGCCACCTACTCTG | 11124 |
rs371887609 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530630 | TTTTAAAATAACTTA[A/G]AGAATGTAATTGGAT | 11124 |
rs371901211 | snp | C/G | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459430 | CCTAGACTTTCTCCT[C/G]GTCCCTCAGACTCAA | 11124 |
rs371916111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50893760 | AAGCCAACCAAGCTT[A/G]TATCCTTCCCTAAAG | 11124 |
rs371931019 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924486 | AAATGACCATACTAC[A/C]CAAAGCAATCTACAG | 11124 |
rs371932304 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545098 | ACGGGGAAATTTTCT[A/G]AATTCCAAACCACAA | 11124 |
rs371932713 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958465 | GGTGGATCACGAGGT[C/T]AGGAGATCAAGACCA | 11124 |
rs371939972 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672019 | TCCAGGGTGGTCTTT[C/T]TTTTTTTTTTTTTTA | 11124 |
rs371954466 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50779567 | TATATTTAGATATGA[-/G]ATAAATATAGAAAAT | 11124 |
rs371960679 | in-del | -/AG/AGAGAGAGAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554390 | TATATATATATATAT[-/AG/AGAGAGAGAG]AGAGAGAGAGAGAGA | 11124 |
rs371967726 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767139 | CCAAAGTGATCTGAT[A/G]GAGCTGAGAAACTCA | 11124 |
rs371991768 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50725922 | ATATGCTTGACTGCA[A/G]GACTAGAGCTCAATA | 11124 |
rs371993037 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50822868 | CAACCTCTGCCTCTC[A/G]GGTTCAAGCGATTCT | 11124 |
rs371995658 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50808104 | GAGGGATTATATTCA[A/G]CATTCTTAAAGAAAA | 11124 |
rs371996853 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50834251 | GCCATGTTTCCTGTA[C/T]GGCCTGCAGAACTGT | 11124 |
rs372010530 | snp | A/C/G | 0.000101448 | 0.00712149 | intron-variant | FAF1 | GRCh38.p7 | 1:50857910 | TGATTACTCATCAGA[A/C/G]AAAGAAAAAAGTACT | 11124 |
rs372017205 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694823 | AAAAAATTGGCCAGG[A/C]GTAGTGGTGGGCACC | 11124 |
rs372019610 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50749543 | ATAATCCCAGCACTT[C/T]GGGAAGCCAAGGTAG | 11124 |
rs372026531 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749570 | GTAGAAGGACAGCTT[C/G]AGCTCAGAAGTTTGA | 11124 |
rs372032162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50487193 | TGCTCTAAAATCTCA[C/T]TGCTAGAAAATGTGG | 11124 |
rs372048904 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449560 | AGTAGCATGATCTCG[G/T]CTCACTGCTACCTCT | 11124 |
rs372061402 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679323 | AAAAAAAAAAAAGTA[A/C]AAAAAAAAAGAATAG | 11124 |
rs372074289 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50834257 | TTTCCTGTACGGCCT[A/G]CAGAACTGTAAGCCA | 11124 |
rs372078349 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50853373 | TATATGACTGTACTA[C/T]AAGCTTCTATTAGTA | 11124 |
rs372088457 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50939720 | CCTAGTCTGTGGAGG[C/G]TTTTTATCATGAAAG | 11124 |
rs372093938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50477441 | TTTATATGGGGAAAT[C/T]GATGCCCAGAAATGG | 11124 |
rs372097232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928288 | CTACTATAAATAATA[A/G]AATGGAAAAGTCTAA | 11124 |
rs372105061 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50720173 | ACCCAGCTAATTTTT[-/T]GTATTTTTAGTAGAG | 11124 |
rs372110211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908660 | TTGATCTTTGTTGGT[G/T]TAAAGTCTGTTTTAT | 11124 |
rs372115737 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50581268 | CATTAGACTGTCAAT[C/T]ATAGCTCTAATTTGA | 11124 |
rs372130771 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50580464 | ATAAAAATATGGCAA[A/T]ATTTTCCTAATTATT | 11124 |
rs372148317 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50704203 | TGAATAGCATTTTTA[G/T]GCTATCTGCTGAATA | 11124 |
rs372149493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50693327 | TTTCTTGGTAATCTT[A/G]CTGAAAATTAATTGA | 11124 |
rs372150670 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50655636 | TTTTCTTCTAGATTC[A/G]AAACAAGAATTTGAA | 11124 |
rs372155267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50757048 | GAATATGTTGTTTAA[C/T]TTCCAAATATACAGG | 11124 |
rs372157258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771935 | ACAAAATGCCAACTA[C/T]GTTTAATTTTGAAAT | 11124 |
rs372167058 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672100 | ACCCAGGCTGGAGTA[C/T]AGTGGCGCGATCTCA | 11124 |
rs372170192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50695901 | TGATCCATTCGCCTC[A/G]TCCTCCCAAAGTACT | 11124 |
rs372172150 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50677809 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 11124 |
rs372172521 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50618435 | TTTTTTTTTTTTTTT[G/T]TATTTTCAGTAGAGA | 11124 |
rs372175336 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50706580 | ATTTTTATCTCCTCC[C/T]GGAACTGTCAATTAT | 11124 |
rs372178426 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447368 | CTGACCTAGTGATCC[A/G]CCCGCCTCGGCCTCC | 11124 |
rs372185579 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50608491 | CCAGGCCATAACCAT[A/G]TATGACATTTCTGTT | 11124 |
rs372190808 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50740398 | AATCTTACACAAGCA[C/T]GGAACATATGGAACT | 11124 |
rs372194994 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50712548 | CTAATCCCAGCTACT[C/T]GGGAGGCTGAGGTAT | 11124 |
rs372198103 | snp | A/G | 0.0001495 | 0.00864453 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50705822 | TGAGAAGTTCAGGTT[A/G]TACTCCCGCTGGACT | 11124 |
rs372198908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543333 | ATGCTCACTGCCTAC[C/T]TACCGTATACCAGGT | 11124 |
rs372211143 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50816205 | TTTTTTTTCCTTTTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs372214566 | snp | A/G | | | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441211 | GCAGGGGGTAGGGGA[A/G]GGTGGCAGAGTTGTA | 11124 |
rs372223940 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950637 | TCAGGCAAACAACAG[G/T]CATCAACTCTATCAT | 11124 |
rs372248460 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50814689 | GGCAAAGGACTTGAA[C/T]AGACATTTCTCCAAA | 11124 |
rs372264887 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50634716 | TGCAATTTAGAGCCA[A/G]TCACTGATTTTTCAG | 11124 |
rs372268515 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50763737 | ATATCACATAATGTA[C/T]CGACATTTTGTTAAT | 11124 |
rs372268610 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746875 | CCACCCTGCACAGAC[A/G]CAGGAAACTGCTCCC | 11124 |
rs372271328 | in-del | -/TC | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50777943 | TCTTCACGCTATGAT[-/TC]AGCAGCTCCACTTGA | 11124 |
rs372273512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50852708 | TGAGCTTGGACAGTT[C/T]ACTTAACTTCATTAG | 11124 |
rs372274705 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50494872 | CAGAAGCCTCTAAGT[A/G]TTCTTCAGTCTAGTA | 11124 |
rs372274899 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50514903 | CTGGTAACCTAGGAT[A/G]GAGCCTGTACATTTT | 11124 |
rs372278182 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936743 | AACCACATGGGATGC[A/G]GTAGAGTGGAAAGGA | 11124 |
rs372281637 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50884178 | CAACAAAGCAACAAA[C/T]TTGTATGTATACATA | 11124 |
rs372282969 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50866668 | CCAGAAGAGAAACTA[C/T]AAAACAATGCTGAAA | 11124 |
rs372295323 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50835737 | ACCAGATATTAAATA[C/T]GTACTTGAAAAACAT | 11124 |
rs372308025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606689 | GTATTTTAGTAGAGA[C/T]GGAGTTTCTCCATGT | 11124 |
rs372318085 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50951410 | CAAAAATAACAGCTA[A/C]AATTTATTGAACACT | 11124 |
rs372320897 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624335 | TGTATTTTTTAGTAG[A/T]GATAGGGTTTCACTG | 11124 |
rs372326854 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50944545 | CAACACCCAGACCTT[C/T]CATCTGGAAATGTCA | 11124 |
rs372329480 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50650593 | CCACCGCACTCCACC[C/T]TGGGTGACAGAGCAA | 11124 |
rs372332935 | in-del | -/GTGTGTGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530239 | TAGCTTTAAGAAGTG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 11124 |
rs372334513 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50814915 | AAATTAAAACCCTTT[G/T]GTACTGCTGATGGGA | 11124 |
rs372335702 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50595123 | GCAATGGCACAATCT[C/T]GGCTCACTACAACCT | 11124 |
rs372339241 | snp | A/G | 0.000106733 | 0.00730446 | intron-variant | FAF1 | GRCh38.p7 | 1:50452154 | GAATATACAAAGAAC[A/G]AGAACAGGCATGTTT | 11124 |
rs372340511 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50728176 | AGAGAGAGGGTATAA[C/T]AGAGGGGCTGTTTTA | 11124 |
rs372348553 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50689270 | CAATTCTACTCCTAG[A/C]TATATAACAAGAGAA | 11124 |
rs372357717 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50904790 | GCCAGTTTCCACAAA[A/C]CTCCTGAAACAAATA | 11124 |
rs372366927 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642744 | TTCCTTTTAATGTAA[G/T]TCATACTTACTGTAA | 11124 |
rs372368801 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50631013 | TCACCATCTTGGCCA[C/G]GCTCCTGACCTCGTA | 11124 |
rs372374634 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642071 | AACCAGGCATGGTGG[C/T]GGGTGCCCGTAATCC | 11124 |
rs372381483 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836157 | TGTGTGTGTGTTTTT[G/T]TTTTTTGTTTCTGTT | 11124 |
rs372403257 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936742 | AAACCACATGGGATG[C/T]GGTAGAGTGGAAAGG | 11124 |
rs372411140 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499008 | AATGGATACACAAAA[C/T]ATGGTATATACCTAC | 11124 |
rs372422349 | snp | A/G | 0.000356014 | 0.0133372 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50539701 | TGCCACAACACTGCC[A/G]AAGTGTCTATTGCAC | 11124 |
rs372424401 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50840909 | TAATGAAATACCACT[C/T]GGTCAAGAAAAAAAT | 11124 |
rs372428817 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50828690 | ACGACATTAAATATA[A/G]AAGGTAAAAACAATG | 11124 |
rs372437538 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50780637 | TCCAGCCTGTCTCTA[A/G]CCAGCTTCCTCACAT | 11124 |
rs372440476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50782200 | TTTTTTTAAGTTAAC[A/G]GTAAAACAGGCTCAG | 11124 |
rs372445264 | in-del | -/GAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674907 | ATTTTATTTTATTTT[-/GAG]ATGCAGTTTCGCTCT | 11124 |
rs372445827 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457504 | AGCGTGTCTGCGAAA[A/G]CAACTAGAATACGGA | 11124 |
rs372448632 | in-del | -/TTTCTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590628 | TTATTTCTTTTTCTT[-/TTTCTT]GCCTAATTGCCCTGG | 11124 |
rs372453485 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50755515 | GCTTTTCCAGGTTCA[C/T]GGTGCAAGCTGTCCG | 11124 |
rs372469291 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50933675 | TACCTTTTCGGCAAC[A/G]CCCCACTGTACTGAT | 11124 |
rs372469503 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50760297 | ACAGAAAGTCAACAA[C/T]GATACCCAGGAATTG | 11124 |
rs372478075 | snp | A/C | 0.000437904 | 0.0147905 | intron-variant | FAF1 | GRCh38.p7 | 1:50959704 | GCTGGGAAGAAGACT[A/C]CCTTGTGGCACCGGA | 11124 |
rs372485951 | snp | C/G/T | 0.000148391 | 0.00861241 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788118 | CATTACAGGTCGAAA[C/G/T]GCTGAAGAAGAAGAG | 11124 |
rs372527083 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50539240 | AACTAAAGATAAGTA[C/T]TTCTTCCAATTAATC | 11124 |
rs372532187 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457446 | CACATTTGCAGTTGT[C/T]TGTGTTTACAATGGG | 11124 |
rs372532554 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50866743 | GGGTAGAATCAATAC[-/T]AGAAAGATGACCATA | 11124 |
rs372543004 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50921497 | CCAGGCATGGTGGCT[C/T]GCGCCTGTAATCCCA | 11124 |
rs372546632 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50864149 | TTGATCCTTTCAAAA[A/T]ACCAGCTCCTGGATT | 11124 |
rs372548756 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50513027 | TTGTATGAGGGCCCA[A/G]AGCAAGCCTCTAGGT | 11124 |
rs372595402 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50643794 | GCTGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 11124 |
rs372596220 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50735045 | AAGAACACCAGGAAT[A/G]AGTTGGTATCTAAGA | 11124 |
rs372603834 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50779333 | TTCTTCATGGTATCT[C/T]AGAATGGTGAGTCCT | 11124 |
rs372607831 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50774498 | TGTTTTAAATCTTTC[A/C]ATATTCAACCTGAGT | 11124 |
rs372616404 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846558 | TAGAGGTTCTGATGG[A/G]AAAAGGAGCAATAGT | 11124 |
rs372634158 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619035 | GTGCTAGGATTACAG[C/G]TGTGAGCCAGCACAC | 11124 |
rs372643944 | in-del | -/GAGTTT | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50496684 | ATCACCTGAAGTCAG[-/GAGTTT]GAGACCAGCCTGACC | 11124 |
rs372655175 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50688668 | AAATACAAAATTAGC[C/T]GGGCGTTGTGGCGCA | 11124 |
rs372690416 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510165 | ACGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs372698752 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50851995 | CCTGAGAATCAGAAC[C/T]GATAAAAACTTTCAA | 11124 |
rs372708080 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50872887 | CTGGGCAACAACAGC[C/G]AAACTCCGTCTGGAA | 11124 |
rs372713139 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50891036 | TCACATAGTCCCATA[C/T]TTCTTGGAGACTTTG | 11124 |
rs372715237 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449133 | CTACTAAACTTCGTT[A/C]TGAAGAATGCATACA | 11124 |
rs372719986 | snp | C/T | 0.000181337 | 0.00952028 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475569 | GCTGGCCAGGAAACG[C/T]CGCTCCAAGAACTCG | 11124 |
rs372726130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50474102 | CACGACACAAGATAT[A/T]CCTTTCTTAGAAAAT | 11124 |
rs372759446 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881677 | TATTTTTGCAGAGCT[C/G]ATGTTGTTTTCCATA | 11124 |
rs372773840 | in-del | -/A/AT/ATAATAA | 0.41507 | 0.187755 | intron-variant | FAF1 | GRCh38.p7 | 1:50931893 | TAAATAAATAAATAA[-/A/AT/ATAATAA]TAATAATAATAATAA | 11124 |
rs372773997 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640869 | AGACTGGGTCTCACT[-/CT]GTCGCCAGGCTGGAG | 11124 |
rs372777926 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50859392 | AAAGGATCCTGGAAC[C/T]GATAACTTCAGTAAA | 11124 |
rs372786177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50531424 | TAGCTTAAAAAACAG[C/T]GCATATAAAAAAATC | 11124 |
rs372786365 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50841969 | ACTAAGAATGCTGGA[C/T]CATTACATTTCCAAA | 11124 |
rs372788373 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50520021 | AGCACAATGCGGATA[C/T]ATAGCAAGTCCCTAA | 11124 |
rs372799502 | in-del | -/AACT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694999 | AAATTGATAGATTCT[-/AACT]GTCAGCAAAATAGAA | 11124 |
rs372802490 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717628 | ACAAATCCAAATTGA[A/T]ATCTCACTCACTAAA | 11124 |
rs372804882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50793913 | ATCTGAAACTTTTTG[A/G]GCACTGACATTAACA | 11124 |
rs372822523 | in-del | -/GTCT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50608958 | TGTGTATCTGAATCT[-/GTCT]ATCAACCAATATATC | 11124 |
rs372825352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50744927 | TAAAATGGGAAATAA[C/T]ATTATTTATCTTATC | 11124 |
rs372845992 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643165 | CTTTTTTCAGCATTG[C/T]GTTTTATCTCTTTTA | 11124 |
rs372862400 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641919 | ATAATATTCCTTGTT[A/C]TGGCCAGGCGCGGGG | 11124 |
rs372868241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50712858 | GTTAAGCCACCTTGG[A/G]GCAGTCTTTTACCTT | 11124 |
rs372880583 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490396 | AAAAAGGAAGGAAGG[-/A]AAGGAAGGAAGGAAG | 11124 |
rs372887611 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50673244 | GCCTGGGAACAGAGC[A/G]AGACTCTGTCTCAAA | 11124 |
rs372897213 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50491186 | TGGAAAAAAATTTCC[A/C]CTGAAACTCCTACTC | 11124 |
rs372897424 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50763669 | TGCTATGTCTTCATA[-/T]TCACTGACCTTTTCA | 11124 |
rs372902044 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50772381 | TCAATCATCACACCA[G/T]AAAAGACACATGTAC | 11124 |
rs372916663 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50715806 | CATTTTACATACCCC[C/T]CCACATTTTTTAAAA | 11124 |
rs372948241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50696709 | AGAATTGGTTTCTCT[A/G]TGTCACTCATGGGAC | 11124 |
rs372961968 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769067 | AAAACAGGAGAGAAA[A/G]AGAGAGAGATAGCTC | 11124 |
rs372971256 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729062 | TATATATATATATTT[A/T]TTTTTTTTTTGAGGC | 11124 |
rs372971644 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731391 | TTTTTTTTTTTTTGA[A/G]ATGGAGTCTCACTCT | 11124 |
rs372971721 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50678932 | CTCTACTAAAAATAC[A/G]AAAAAGTAGCCAGGC | 11124 |
rs372977926 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50523229 | TGCAATGAACTTTCA[A/G]GCACAAATACCTATT | 11124 |
rs372979165 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50713961 | TATTTTTAGTTGAGA[C/T]GGGGTTTCACCATCT | 11124 |
rs372993143 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50776917 | TTGTAAAGATAAATA[A/T]CATTACTTTTAAAAC | 11124 |
rs373001905 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50770847 | GAGGCACCACATTAC[A/C]CAACTTCAAACTATA | 11124 |
rs373004858 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789143 | CCCAGGCTAAAATAA[C/T]CTCCTCATTAGCTCT | 11124 |
rs373008181 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50833493 | ACCAATCTGGAAGCT[C/G]TCCAAATCCTGTTGT | 11124 |
rs373016910 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50891982 | AGAGGCAGGCAGGCC[A/T]CCTTGAGCTGCAGTG | 11124 |
rs373024619 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50760790 | GAACTAGAAAAGCAA[A/G]AGCAAACACATTCAA | 11124 |
rs373026982 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50805239 | CTTGCCTTGACCTAG[A/T]TTATACTCATTTGAA | 11124 |
rs373032940 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50904509 | AAATTATTAAAATGA[C/T]AGATTTTATGTTATG | 11124 |
rs373037636 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50447157 | TTGAGATGGAGTCTC[C/G/T]CTCTGTTGTCCAGGC | 11124 |
rs373040763 | snp | C/T | 5.26385e-05 | 0.00512996 | intron-variant | FAF1 | GRCh38.p7 | 1:50596260 | AACAAAATACGGCCA[C/T]GTTTCACAAAAGGAT | 11124 |
rs373086243 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50879176 | CTTGAACCCGGGAGG[C/T]GGAGTCTACAGTGAG | 11124 |
rs373102999 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447291 | CCACCACGCCTGGCT[A/C]ATTTTTTGTATTTTT | 11124 |
rs373107148 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543967 | GGATCCATGTGGAAA[C/G]GGCATCCTCCCTTTA | 11124 |
rs373108605 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50535254 | TGGTAAATTTGGAAA[C/T]GCATCTTCATCATCC | 11124 |
rs373110012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50758020 | CCTCTGACATTCAAC[C/T]GATTCTCGTGCCTCA | 11124 |
rs373112008 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50861591 | ACAAAAATGCTACTT[A/C]TTGGGTACAGTGTAC | 11124 |
rs373113215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714006 | TGGAACTCCTGACCT[C/T]GTGATCCACCCGCCT | 11124 |
rs373116880 | in-del | -/CAACCAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724256 | AAAAAAAAAAAAAAA[-/CAACCAT]ATATATATACATATA | 11124 |
rs373136849 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50644293 | CTGAATGCCCTGTGT[A/G]TTCACTGAGGTGTCT | 11124 |
rs373145150 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50502227 | AGACTCAAAGGAAGA[A/G]TGTGCTTAGAACTGA | 11124 |
rs373152115 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50732838 | CTGTTTGCTGATGTA[C/T]TGACTGAGTTCCTCA | 11124 |
rs373159035 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929461 | TGTATTCAGATCCCT[C/T]CAAAAAAATAAAAAT | 11124 |
rs373161973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50717118 | CGCGGCTTCATTCTT[A/G]GAGTCAGCGAGAACA | 11124 |
rs373165684 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50442303 | CACAATGTTTAAAAG[C/T]TGAGTAATACTGGTT | 11124 |
rs373166530 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819612 | GCCTGGTCAACAGAG[C/T]AAGACTGACCGACTG | 11124 |
rs373170134 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50838755 | TATTTTGAAAACTCC[G/T]TAAATGTGATAACTA | 11124 |
rs373179755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50879386 | GGTGAATACAAAGAT[A/G]ACCATATATTCCCTA | 11124 |
rs373183379 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50846797 | AGGGATTGTCCCAAT[C/G]CCACTTAAAGGAAAA | 11124 |
rs373184788 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50913930 | ATTGGTTTTTCAGGT[A/G]TCCTACCAGGAAGAA | 11124 |
rs373215675 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50716455 | GAGAGGTGAAGCCAG[C/T]TGGACTTCCTGGGTC | 11124 |
rs373237000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758683 | GGTGCTTACTTTAAC[A/G]TCTCTTATAGCTTTT | 11124 |
rs373244599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50599144 | TTGAGAGGGAACCTC[A/G]CTCTGTCACCCAGGC | 11124 |
rs373246654 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50625170 | TTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 11124 |
rs373258777 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50680494 | TTGAGACCAGCCTGG[C/T]CAAACTGGGGAAACC | 11124 |
rs373265389 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50858252 | TTTAAATTTTGAGCT[C/T]TGATACCCAGGATGA | 11124 |
rs373270248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523553 | AGCTTGTTGGTCATC[C/T]GTATATCTTTGAAGA | 11124 |
rs373277561 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50485707 | AAAAACCAAAAAAAC[A/C]AAAAAACAACCTGAG | 11124 |
rs373280665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909749 | TTAAGGTCTTCTCTA[C/T]GCTGTTTATTCTGGT | 11124 |
rs373283969 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50900363 | TTCAATTATTCTAAT[A/C]TTTGGGGAAATTAAG | 11124 |
rs373296955 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447251 | CTGCCTCAGCCTCCC[A/G]AGTAGCTAGGACTAC | 11124 |
rs373303991 | snp | G/T | 6.6433e-05 | 0.00576299 | intron-variant | FAF1 | GRCh38.p7 | 1:50584852 | TTCATATTGATTTTG[G/T]CCTATCAAATTCTAA | 11124 |
rs373339737 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800344 | AAAAGTGGCAATAAC[A/G]TTTACTCAAAAATAA | 11124 |
rs373343385 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661062 | ACAATAGAAAAAAAT[A/G]TAACAGACATCAAAA | 11124 |
rs373353168 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836503 | ACTGTCCTAATATTA[C/T]AGTTTATTCTTTGTG | 11124 |
rs373356310 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50895778 | TCATATCGACAGAAT[A/G]AAGGACAAAAACCAT | 11124 |
rs373360003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50856262 | TTTTTAACCACCCCA[A/G]TAACTTCCATCAGCC | 11124 |
rs373392349 | in-del | -/ACTG | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50499518 | TATATCATAAATTAC[-/ACTG]ACTGATTTTCAAATC | 11124 |
rs373412962 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803543 | GGCCTGTCTGGCATA[C/G]TGTCTGCACAATAAA | 11124 |
rs373414046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940863 | TTTTTGGGAAGATTT[C/T]GTTTCTCCATCTCTC | 11124 |
rs373425527 | in-del | -/T | 0.458775 | 0.137524 | intron-variant | FAF1 | GRCh38.p7 | 1:50449490 | ACAACTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 11124 |
rs373435438 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661105 | AATAATTTCACATGA[C/G]AAATAAAGATAATAA | 11124 |
rs373443539 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50495651 | TTGCTGGATCATATG[G/T]TAGCTCTATTTTTAG | 11124 |
rs373451601 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50886606 | ATTGATCAATTCCCA[A/C]CTATGAGTGAGAACA | 11124 |
rs373463479 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50471678 | TAGAACAGGGGCTGT[A/G]TCATTATATCAGTGG | 11124 |
rs373471070 | in-del | -/GA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927015 | AAGCCAGACATAAAA[-/GA]ACAAACACTAAATAA | 11124 |
rs373477724 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894185 | ATGCCTGTAATCCCA[A/G]CTACTCAGGAGGCTG | 11124 |
rs373487022 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50566871 | TTTCAGGTTATTCTT[C/G]AATTTAAAAAGTTTT | 11124 |
rs373489124 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50765194 | TATTTGCCTGCCCAG[A/G]AGAGAAATAATTAGC | 11124 |
rs373520384 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50791198 | GGCAGGAAAGAATGC[C/T]ACAGCTGAAATCCAA | 11124 |
rs373539016 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50827732 | AAGAATACCTAAATA[C/T]GTAAATAAAATATCT | 11124 |
rs373551091 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50733108 | GATTTATTATGATGA[C/G]CTAATAAGATAACAT | 11124 |
rs373561387 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50933356 | AGATACCCTAAATCA[C/T]CTCCCTCAAGTTCAA | 11124 |
rs373564121 | in-del | -/CC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50796231 | ACACACACACACCCC[-/CC]TATCTTCTTGCAGTT | 11124 |
rs373565854 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50879288 | AATGAATGAATGAAT[-/C]AGATTAATGTAATTC | 11124 |
rs373571671 | in-del | -/GA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50891324 | TTCCTTTAGCCCAGA[-/GA]AGTTTGGTCTTCTGA | 11124 |
rs373578502 | in-del | -/GGAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561849 | GATGGACGGATGGAC[-/GGAA]GGAAGGAAGGAAGGA | 11124 |
rs373581373 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637296 | AAAAAAAAAAAAAAA[-/T]ACAAAAATTAGCCAG | 11124 |
rs373584579 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50886624 | ATGAGTGAGAACATG[A/T]GGTGTTTGGTTTTTT | 11124 |
rs373601259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756687 | GGTTTAACGGACTTA[C/T]AGTTCCACATGGTTG | 11124 |
rs373602208 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50678903 | CCATCCTGGCTAACA[-/T]GGTGAAACCCCATCT | 11124 |
rs373603609 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467526 | CACCATGTTAGCCAG[A/G]ACGGTCTCGATCTCC | 11124 |
rs373606089 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50795280 | GGGCAGTGATCTATC[C/T]TCTCTGAAAAAGACA | 11124 |
rs373623036 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836528 | TTTGTGGAGATTTTG[A/T]CCCCAGCTTTTTAAA | 11124 |
rs373627352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50789785 | TAAAGTGGCGTATGA[C/G]GCCCTGTATGATCTG | 11124 |
rs373628659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516530 | ATTTTACCAACTAAA[C/T]TATATTCAGTGGTTA | 11124 |
rs373648010 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50825457 | GGGAGGTCTTTTTCA[C/T]AATGATAAAAGGGTC | 11124 |
rs373651306 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50546314 | AAGGTATTAAATTGT[-/GT]TTACCATTTGTGTAA | 11124 |
rs373655164 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50669756 | GTTCTTTGTGCTGTC[C/T]AATATAGTGGCCATT | 11124 |
rs373674975 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50923270 | AAAAAATATTCCAAA[A/G]AAATTTAGCCAGGCA | 11124 |
rs373697889 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679056 | GGTGCCACTGCACTC[C/T]AGCCTGGGTGACAGA | 11124 |
rs373698484 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50761064 | ACTACAAACACCTCT[A/G]TGCAAATAAACTAGA | 11124 |
rs373699141 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872083 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAATACAT | 11124 |
rs373716477 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50737645 | ATAAAGAGCAATCCA[A/G]GAACTCTTTAAATTC | 11124 |
rs373775552 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748470 | CCACTGCACCTAGAT[A/G]ACAAGAGTGAAACTC | 11124 |
rs373789071 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767820 | ATATGGAAAGGAAAG[A/T]CCATTACTAGACACC | 11124 |
rs373791397 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50630043 | AGCCTGGCGACAGAG[A/C/T]GAGCCTCTGTCTCAA | 11124 |
rs373798883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50694551 | CTATAACACTATAGC[C/T]AGGAAAAAAAAAAAA | 11124 |
rs373804697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50870285 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAATA | 11124 |
rs373813398 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50625195 | GTGAGCCACCGCTCC[C/T]GGCAGAGAATCCTAC | 11124 |
rs373818944 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50505262 | TGAACAGACACCTCA[A/C]AATAGGTTCCCAAAT | 11124 |
rs373819414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722415 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAT | 11124 |
rs373825122 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50888921 | TTTCTATTGATTGGA[A/G]TAGTTTCAGAAGGAA | 11124 |
rs373827781 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50588199 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACGTGGG | 11124 |
rs373846971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50638842 | GCTTTGAAAAAAAAC[C/T]TATTTTTATGAAAGA | 11124 |
rs373860340 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50512040 | GCCACATAAAAGTCT[A/T]CTTTTGAGAAGTGTC | 11124 |
rs373861440 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50920523 | CATAGATGCAAAAAT[C/T]CTTAACAAAATATTA | 11124 |
rs373863450 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50549138 | ATGCTTGCCACTGTA[C/T]TATACTGCTGCATAA | 11124 |
rs373869477 | snp | A/G | 0.000118336 | 0.00769117 | missense | FAF1 | GRCh38.p7 | 1:50539676 | CCGTTTTTTGAGTCC[A/G]AATGGTTTGTGCCAC | 11124 |
rs373871776 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50453990 | CTTTTTGTCCTCTGA[A/G]ATTCCTTGTCTGTTA | 11124 |
rs373896240 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643462 | GAACAGTTTCTATTG[C/T]TGTATCTTTAAATTC | 11124 |
rs373902598 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922847 | AAAAAAAAGGCAAAA[A/G]ATCAAAAAAGTTGGT | 11124 |
rs373906664 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958220 | ACCTACAAAACATCA[A/C]AATCTTATGGTCAAC | 11124 |
rs373914670 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50647089 | CCTGGTCTCAAGCAA[C/T]CCACCTGCCTCAGCC | 11124 |
rs373929599 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951430 | TATTGAACACTTTCT[A/G]TGTCAGACACCTTTT | 11124 |
rs373930755 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50664265 | CTTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 11124 |
rs373933763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451651 | TCCCCCATAACAGAG[C/T]GTATTATTACCTTAG | 11124 |
rs373943871 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50792683 | CCATGAGGTCCTGGA[C/G]GATACTGCATTAAAG | 11124 |
rs373946456 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467317 | TCATTTACACATTGA[A/G]AGTATTTTTCTTTTT | 11124 |
rs373958244 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739772 | TACCTATATATCTTT[C/T]ACTCCAGATATCTTT | 11124 |
rs373958364 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676875 | TTTAAGACATTAACA[C/T]TTGAGATATAGGAGT | 11124 |
rs373961890 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50654721 | AATGATTAGCTTGAT[C/T]TTGAAATATCTGTAA | 11124 |
rs373964123 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50721033 | ATTAAGTATGTTTTC[A/C]TCTTGTTAATCTGTT | 11124 |
rs373965695 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50611426 | AAGTGCAAAATAATC[C/T]CAAAATTATGCCACC | 11124 |
rs373972776 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50695717 | CAGTGGCGCGATCTC[C/G]GCTCACTTGCAACCT | 11124 |
rs373987580 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917357 | AGCTGACTTCTGCTA[C/G]GGACTTTTTAATTCC | 11124 |
rs373994448 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50589969 | GGATTAGTGCCCTTG[C/T]CAAAAACCATTTTAT | 11124 |
rs373998567 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50658453 | TACAACAATAAAGTA[C/T]TATGAAATAAACAGT | 11124 |
rs374012420 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748404 | CAGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC | 11124 |
rs374016862 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50579962 | TTGTTATATGTGAAA[A/G]TGGTATTGTGATTAT | 11124 |
rs374021590 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950904 | GCTGACAAATTAGCT[A/G]GAAAATGAACACTCT | 11124 |
rs374027359 | snp | A/G | | | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440903 | CATCTTAGTAAAGCC[A/G]TCAGAAAGTTCTAAC | 11124 |
rs374029682 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907011 | GTATGATATTGGCTG[G/T]GGGTTTGTCATAAAT | 11124 |
rs374031621 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50866413 | CTGTTGATGTTTGCC[A/G]ATGATATAATTGTAT | 11124 |
rs374035439 | snp | C/T | 3.39876e-05 | 0.00412221 | intron-variant | FAF1 | GRCh38.p7 | 1:50858029 | TAAGCATTTTACATA[C/T]AATTTTAGAAATAGG | 11124 |
rs374039528 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50883341 | GCTAAAGTATCACCC[C/T]CAGATTACTTGCTAA | 11124 |
rs374058025 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50455741 | AAGTGGCTAGAAGAA[C/T]TAAAATTTTGCCCCA | 11124 |
rs374063167 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881524 | TCCCTCACACTACCA[A/C]AAGAAGGAACATCCA | 11124 |
rs374068953 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50861233 | TGAAAAACAAAACAC[C/T]AGTAGACCACATATT | 11124 |
rs374071519 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50753757 | ATGTCATTATCTGTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs374073361 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50622173 | CCATCTCAAAAAAAA[A/G/T]AAAATAAAAAGAAAA | 11124 |
rs374074100 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872781 | GGTGGGTGCCTGTAA[A/T]CCCAGCTACTCAGGA | 11124 |
rs374087163 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50718324 | TGAGGCACCGTGCCC[A/C/G]GCCACAATCCACTTT | 11124 |
rs374087774 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50614944 | TCAACTTTTATGTTA[A/G]ACACAGGGAGTACAT | 11124 |
rs374088035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50567013 | AATGTTTATGATGAT[A/G]ATAAACACAATGATT | 11124 |
rs374095313 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50870147 | TCTACAGCACCGTGA[A/T]GATATTGCATTTTTA | 11124 |
rs374102466 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50453683 | ACCAAACCTATACCC[A/C]AAATTCCCAAACTCC | 11124 |
rs374113479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858195 | CAAAGTAAATTTACA[C/T]TGCTCTGAAAAAAAG | 11124 |
rs374113874 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707071 | AGCCAGGTGTGGTGG[C/T]GGGCACCTGTAGTCC | 11124 |
rs374124922 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649745 | CAGGAGTTCAAGACC[A/G]GCCTGGCCAACTTAT | 11124 |
rs374134767 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50952310 | AGACGGGTTTTCGCC[A/G]TGTTGGCCGGGCTGG | 11124 |
rs374146304 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749805 | GAGAAAAAAAAAAAA[-/A]CACGATTCTCAGCCT | 11124 |
rs374156944 | snp | A/G | 0.000115824 | 0.00760911 | intron-variant | FAF1 | GRCh38.p7 | 1:50959745 | GTTGGAAGTGGGAGG[A/G]GAAGAGGGCCAGATA | 11124 |
rs374162629 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50818680 | ATGCTTGGGACCAGA[A/C]TCATTTTGGATTTTG | 11124 |
rs374167406 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50743042 | TTCACATATTGTCTA[C/T]GGCTGCTTTCCCACT | 11124 |
rs374169503 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50759545 | TTTTCTTAATCCAGT[C/T]TATCATTGTTGGACA | 11124 |
rs374181428 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50943492 | CAGGGCAATTTTATC[A/G]TCCATAATAACTCTT | 11124 |
rs374191387 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50633215 | GGGTGCATTTACTTA[C/T]TAAACAAGTGGCTAA | 11124 |
rs374193216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50952576 | GGCCACCCATCGTCT[A/G]GGATGTGAGGAGCCC | 11124 |
rs374193522 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746784 | AAAGGCCTCACAGGC[A/G]TTTCACAGACCTTCA | 11124 |
rs374209600 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50606165 | TAGGTGTTTTCAGTT[G/T]CAATGCCCAATTATT | 11124 |
rs374211591 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683002 | CACACCACTACACTC[C/T]AGCCTGGTGACAGAG | 11124 |
rs374213310 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50527093 | AACTCCCAGCCTCAA[C/G]TATCTGCCCACCTCG | 11124 |
rs374217344 | snp | A/G | | | synonymous-codon | FAF1 | GRCh38.p7 | 1:50535405 | TTGTTGGGCTGTGAA[A/G]ATCTCCATTGCAGCC | 11124 |
rs374218251 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50518678 | ATCTCCTGACCTTGT[C/G]ATCTGCCCACCTCGG | 11124 |
rs374229051 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50488554 | AAACTATATTTCTTG[A/G]AATAGCCTAAAAGGA | 11124 |
rs374236158 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50511930 | TGACTTTTTAATGAT[C/T]GCCATTCTAACTGGC | 11124 |
rs374243594 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50465120 | GAAAGAATCACTACC[A/G]TCACATTTAAGTGCC | 11124 |
rs374252707 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50864062 | ATATCCCCTTTATCA[-/T]TTTTTATTGTGTCTA | 11124 |
rs374255138 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50895501 | AAAAACAGAGGAGAA[C/T]ACTTACAAACTCATT | 11124 |
rs374257469 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953861 | TACAGAAAACATAAC[C/T]GAAAATAACATCAAA | 11124 |
rs374262419 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50573458 | TAAAAAAGATAAAAA[A/G]CAAAGGAAAAGTTTG | 11124 |
rs374267575 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50549265 | TTAACGTTGTCATGT[C/T]CCCTAAATTTTCTAG | 11124 |
rs374267881 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50705076 | AGGTGTAATGCAACA[C/T]AGTCATCATTTCAAT | 11124 |
rs374269031 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50628418 | TGTTCAGTATAAGGA[A/G]CTCCCAAGTTTTAAT | 11124 |
rs374275583 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50571000 | TTTCTATTACTATAA[C/T]CAGTTTTTCCTTTGG | 11124 |
rs374280124 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50546749 | TAGATATGGGTTTAA[C/G]AAGGAGACTTTTTAT | 11124 |
rs374333702 | snp | A/C | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459676 | TTAGTACTGTCTCCC[A/C]CAGCCTGTTTAATTT | 11124 |
rs374336408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807178 | GAGATAAAAGACAAA[C/T]GGCAATTGTAAGAAA | 11124 |
rs374339822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50516382 | AACAGCTTCAGGTAC[C/T]GAGTTTTCATTTTTA | 11124 |
rs374374807 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951085 | AAAATATTTAAAAAG[C/T]TAGCTGGATGTGGTG | 11124 |
rs374379809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777577 | GAAAAAACACAGATA[C/T]GGTAAACTATACCAG | 11124 |
rs374386797 | snp | A/G | 3.35447e-05 | 0.00409527 | intron-variant | FAF1 | GRCh38.p7 | 1:50787972 | TAATTATTTATTTGT[A/G]AAGGCTTTATGGCAG | 11124 |
rs374396881 | snp | A/G | 4.95413e-05 | 0.00497677 | intron-variant | FAF1 | GRCh38.p7 | 1:50801598 | TCTTTGTTCTGCTAA[A/G]TCATCTTAACTGGTA | 11124 |
rs374400872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462346 | TTACCAAGAAATTAA[A/G]TAACCTAAGATCACT | 11124 |
rs374403060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50801266 | TAGTAAGCCTGGAGA[C/T]AAAGCCTGTATAGTT | 11124 |
rs374412408 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50479385 | ACTCTGCTTCTAATC[A/G]GCCATCTTGGCGCTG | 11124 |
rs374419981 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50774368 | ATTTGCCAAACACTA[C/T]ACAGCTAATAAGAGT | 11124 |
rs374425428 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50702327 | AACTGTTGACAAATC[G/T]GAATTCTCAGCGTAA | 11124 |
rs374428212 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50758413 | AGAAATCTGTCTTAC[G/T]ACAGAATACTTCTAG | 11124 |
rs374429958 | snp | C/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50759721 | AGATCCCTGAGGAAT[C/G/T]GCCACACTGACTTCC | 11124 |
rs374453674 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50575597 | ATTATTTGTATAATT[A/C]AAATATATTTTTCTA | 11124 |
rs374461640 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50744019 | GAGTTTGCAGTGAGG[C/T]GAGATCATGCCACTA | 11124 |
rs374467317 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50791533 | GACTTCTTTTTTCCT[G/T]CTTGCATTCATTTCC | 11124 |
rs374472769 | snp | A/G/T | 0.000139384 | 0.00834709 | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959858 | GAAGCGCGCACCTGG[A/G/T]AGGCAGACGGCACCT | 11124 |
rs374486608 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927901 | TTTTTTCTACTCGTT[A/C]CATATTCTGTTCTTT | 11124 |
rs374501349 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50610127 | ATTGATCAAATCTTC[C/G]GTGGTTCTTACTGTA | 11124 |
rs374503228 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938114 | CTCTGACCACAATGC[C/T]AACCATACCACTAAG | 11124 |
rs374505604 | in-del | -/AG/TA | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50637915 | AAGATAAATTTGTGT[-/AG/TA]ATATATATATATACA | 11124 |
rs374510055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50503177 | GCAAAATTTTTAAAT[A/G]TAAAGGTTAAATTAT | 11124 |
rs374510990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725736 | GCTGGGATTATAGGC[A/G]TGAGCCACCACACCT | 11124 |
rs374522095 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50759945 | TTTGGCTGCATAAAT[A/G]TCTTCTTTTGAGAAG | 11124 |
rs374525317 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50636321 | TCTAGTCAACTACCA[C/T]ACCTGATCTGAGGCA | 11124 |
rs374529349 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863968 | TTTATCCATTTCTTC[C/T]AGATTTTCTAGTTTA | 11124 |
rs374530522 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50748698 | AATCAGAATGTACTT[A/C]TCTTTCATATATCTG | 11124 |
rs374533866 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50738036 | TTAAACAATAAAAAA[C/T]GTAATGTATAATTAA | 11124 |
rs374534805 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50661215 | TATGAGATCTCATTT[-/A]AAAATAAAGCCTGTC | 11124 |
rs374535204 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50506166 | AATAATTTCTAATTA[C/T]AGACACAAAAAACCC | 11124 |
rs374543486 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50839113 | ATAAAAATAAATATA[C/T]GTTTATTATATTTAT | 11124 |
rs374545853 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50476424 | TCTGGACCTACAGAT[A/G]GACCAAACCCTTCAT | 11124 |
rs374548408 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787946 | AAAAAAATATAACCT[A/G]AATGTTTACCTAATT | 11124 |
rs374554882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671538 | TAGATGTTACTGTAA[A/T]AGATAATGTTAACTA | 11124 |
rs374556580 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953963 | ACATTTTTTTTTTTT[A/T]TTTGAGACGGAGTCT | 11124 |
rs374570336 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510764 | ATTTCAAAAAGGTTT[C/G]TCTTTTTTTTAAGGA | 11124 |
rs374573312 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50571679 | TCTTCACATTCAAAT[C/G]CAGGAGCTAAGGTAC | 11124 |
rs374575473 | snp | C/T | 3.30344e-05 | 0.004064 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50801654 | AATGCCATTTTCCTG[C/T]GGTATTACACCATTG | 11124 |
rs374579559 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530750 | CATTTCATGTACTCC[A/G]TAAACATATACACCT | 11124 |
rs374582460 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766005 | GCTGAGGCAGAAGAA[C/T]AGCTTGAACCCGGGA | 11124 |
rs374626972 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50822039 | TTTCTTTTTATTAAC[C/T]CTGCTGTATATTTTT | 11124 |
rs374641137 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569746 | GACTTTGGGAAAGAG[A/T]TTAGTGATTTACATT | 11124 |
rs374657055 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50682287 | GGCCCATCGCTTGAG[C/T]CCAGGAGTTCCAGAC | 11124 |
rs374659634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50703702 | ATGACATTTAGAAAA[C/T]GGTATAAAAAAGATT | 11124 |
rs374665574 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50704036 | TCACCGAACATTAAT[G/T]AATATTTTATGTCTT | 11124 |
rs374685901 | snp | C/T | 1.67337e-05 | 0.00289251 | missense | FAF1 | GRCh38.p7 | 1:50583701 | CATCTCCTTCATTTT[C/T]TGCGTTTTCTGGCAC | 11124 |
rs374698092 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499362 | GATGTTAGCTGTAGG[-/GT]GTTTTTTTTTTTTTT | 11124 |
rs374704139 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50710672 | CAGTGGTGCGACCTC[A/G]GCTCACTGAAACCTC | 11124 |
rs374710213 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50777743 | CTGAATTCATTTTAA[A/G]AAAAAAAAAAAAAAA | 11124 |
rs374714827 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679635 | ATATTTAGAGATCAT[C/T]TTTCATTCCCCTGAA | 11124 |
rs374744642 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50633806 | GTTGCCTGTCAAACC[C/T]CCGTGAGGTTTGATA | 11124 |
rs374746264 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50781169 | GGTCTACCCTGCCTG[C/T]ACCTCTTTGGCCAAC | 11124 |
rs374746753 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50925276 | TGCTGGGTGGAATCA[C/T]GTCAGGACAAAAACA | 11124 |
rs374750095 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50852475 | TATTTGAAAACAAAG[C/T]AGAAATGTATTTAGA | 11124 |
rs374799361 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875876 | CCCAGACTCTAGTTT[C/T]GATAAAACCAGTCAT | 11124 |
rs374805834 | snp | A/G | 0.000153988 | 0.00877328 | missense | FAF1 | GRCh38.p7 | 1:50705862 | GTGATGATCAGCATG[A/G]AGTTTTGATTTAATG | 11124 |
rs374821594 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50558524 | TCATAATCAAGATAC[C/G]TAGAATATTCAAAAA | 11124 |
rs374826669 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50930839 | AGCACCAAATAGCCC[A/C]ATTTTACAATAAGAA | 11124 |
rs374838455 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50587469 | ATATTTTTTTATCAG[C/T]CATCTAACAGGTTAG | 11124 |
rs374848406 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50540415 | TCATCCTAAAAAACA[A/G]AATTTAGCAACGTTT | 11124 |
rs374852258 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50510098 | TTGAACCTGGGAGGC[A/G]GGGGTTGCAGTGAGC | 11124 |
rs374862776 | in-del | -/AT | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50718533 | ATTCCTGTTATGTGC[-/AT]ATGTTATTTCTTTTC | 11124 |
rs374868052 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50864675 | CCTTCCTTACACCTT[A/C]TACAAAAATCAATTC | 11124 |
rs374875004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909054 | TTCCTTCAGAAGCTC[C/T]TGTAAGGTAGGCCTG | 11124 |
rs374885647 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50939059 | TTTGGGCTCATTTTT[C/G]CTTCCATGTGAATTT | 11124 |
rs374887221 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50563580 | CTCCAATTTAGATAT[A/G]CAATATTGAAATTAT | 11124 |
rs374909561 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50755766 | ACCTCAATTCTTGAC[C/T]TCTGTGCACTTGCAG | 11124 |
rs374918190 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50776336 | TAAACCAATATGTAT[C/G]TACTCCTGCTTCTAG | 11124 |
rs374920219 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50802214 | TCCTGCCTCAGCCTC[C/T]TGAATAGCTAGGATT | 11124 |
rs374924889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50515593 | GTATTATCATAAAGA[C/T]AGGAACAAAGTGAGT | 11124 |
rs374924901 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50898956 | CTTCTCTCCCCTCCC[A/G]TTTCTGCCTTCTGCA | 11124 |
rs374934369 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692126 | GTGGCTGAGATGGGA[A/G]GATCAATGGAACCCG | 11124 |
rs374937721 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820868 | GTGTGTGTGTGTGTA[C/T]ACATACCAGATTTTC | 11124 |
rs374949229 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676972 | AAGGGCAATAAAATA[C/T]ACACAGCAACAAATA | 11124 |
rs374951537 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812172 | GACAAACACGCCAAA[-/A]GCAACTGCAACAAAA | 11124 |
rs374957053 | snp | A/C/G/T | 0.00172445 | 0.0293223 | intron-variant | FAF1 | GRCh38.p7 | 1:50452153 | TGAATATACAAAGAA[A/C/G/T]GAGAACAGGCATGTT | 11124 |
rs374964406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50785206 | AGAGAGGAAATGCTT[C/T]ATAACACTGATCTTG | 11124 |
rs374975545 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50781475 | CCATAAATATATATG[C/T]ATCCAATACTGAAGT | 11124 |
rs374981346 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50679527 | TAACAGACAATAAAT[A/C]AAAAGGTAATATAGC | 11124 |
rs374986413 | in-del | -/TA | 0.276267 | 0.248616 | intron-variant | FAF1 | GRCh38.p7 | 1:50594888 | AAAAAAAAAAAAAAT[-/TA]TATATATATATATAT | 11124 |
rs374990480 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50501964 | GAAATAATCCAAATA[C/T]CCATCAACAGGTGAA | 11124 |
rs375000214 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50793103 | TATAAACAGTAGAAA[C/T]CCCAGACTTGGTAGC | 11124 |
rs375003896 | snp | C/G | 3.295e-05 | 0.00405881 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50655469 | AGCAGAAGTTGGCCA[C/G]CCCTCCCATAATTGG | 11124 |
rs375006695 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FAF1 | GRCh38.p7 | 1:50700316 | GGTTCTTTTCCCCCC[C/T]CTCTCTCTCTCTTCT | 11124 |
rs375011318 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769625 | TTTATCCCTGGGATG[C/T]AAGGTTGGTTTAATA | 11124 |
rs375018164 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50566639 | ATCAATTAGCATATG[C/T]TAGAGTTAAGCTATT | 11124 |
rs375024176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50879620 | AAAACGGGAAAATAC[A/G]TCAGATTTACAAATG | 11124 |
rs375024941 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50544912 | ATTGAAGTTGGAAAG[C/T]ATCTAGCATATTTGA | 11124 |
rs375028879 | snp | C/T | 0.000131985 | 0.0081225 | intron-variant | FAF1 | GRCh38.p7 | 1:50490710 | CTTAACACATACTTG[C/T]TTACAAAGAAAGAGA | 11124 |
rs375035117 | in-del | -/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961043 | TTATTTATTTATTTA[-/T]TTATTATTTTGAGAC | 11124 |
rs375036926 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828641 | CAAACTTCAGGCTCT[C/T]TTATACCAACACAAA | 11124 |
rs375037535 | snp | A/G | 1.68937e-05 | 0.0029063 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50539677 | CGTTTTTTGAGTCCG[A/G]ATGGTTTGTGCCACA | 11124 |
rs375062788 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457345 | GGGAATCTACCATTT[A/G]ATGCATGTGCTAATG | 11124 |
rs375071397 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945531 | TCAGTTTATGATAGT[C/T]GATATTCGTCATATC | 11124 |
rs375077404 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543303 | ATTTAGGGGAAGGGA[C/G]ATGAAATTCCACAAA | 11124 |
rs375081495 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672284 | CTGACCTTGTGATCC[A/C]CCCGCCTCAGCTTCC | 11124 |
rs375082749 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50552187 | TTGTAGTCCCAGCTA[C/T]TCAGGAGGTTGAGGC | 11124 |
rs375085119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50853063 | CAGTGCTCAATGCTT[A/G]GCTGCTTTCGGATGA | 11124 |
rs375092505 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717562 | TAGGGCCTCTGTATT[C/G]ATAGTACTCAAGTAA | 11124 |
rs375097584 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701618 | AGAATAATAGACACA[A/G]CATACAAAATCCGAC | 11124 |
rs375099640 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50798027 | TTGTTTATTATTTCA[A/G]TTCTTTAAAGTCCAT | 11124 |
rs375102732 | snp | A/G | 1.67228e-05 | 0.00289156 | intron-variant | FAF1 | GRCh38.p7 | 1:50787975 | TTATTTATTTGTGAA[A/G]GCTTTATGGCAGGAA | 11124 |
rs375104491 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50520948 | TCTTTGCTAGGGATA[C/T]TTTTTGTAAGGATAT | 11124 |
rs375105233 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50767834 | GACCATTACTAGACA[C/T]CACAAAAACTCACTT | 11124 |
rs375107904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50556110 | GGGCTTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 11124 |
rs375114106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744829 | TAACACAGTTAACAT[C/T]TGTCCATATCCAGAG | 11124 |
rs375126492 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50823212 | AAGGAAAACACTCTT[C/T]CTTGTTAACAGCAAC | 11124 |
rs375128689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50887604 | TACATATGGCTAGCC[A/G]GTTTTCCCAGCACCA | 11124 |
rs375136296 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50547918 | ATAAACATTTAAGTA[C/T]TTGAAAATTTCTTCA | 11124 |
rs375158728 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50867715 | GGTGAAAATAGAACA[C/G]TTTTACACTGCTGGT | 11124 |
rs375162086 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50577051 | ATTTTATCAGCATCA[C/T]GCCTAGCAATGCAAC | 11124 |
rs375217538 | in-del | -/GAAGA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50922511 | GAAGAGAAGAGAAGA[-/GAAGA]AAAGAAAACCACCAA | 11124 |
rs375221339 | snp | A/G | 1.79906e-05 | 0.00299916 | intron-variant | FAF1 | GRCh38.p7 | 1:50452198 | AGTCCTGGAATCTGG[A/G]AGACATAATTTCAAG | 11124 |
rs375249217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525824 | AGTATCAGAGTTACA[G/T]ATTATGTTGCATAAT | 11124 |
rs375266019 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50474249 | CTGAAGACAACAATC[A/G]CATCTCTCATGGTCC | 11124 |
rs375270994 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50790580 | ACTTAATTTATCTTA[C/T]GTATTGCCACTTCTT | 11124 |
rs375282531 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499682 | AAGTGAGTTTAGTAA[A/G]GTTGCAGAATATAAA | 11124 |
rs375286383 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50794947 | TGGCTAAATATATTT[A/G]TTTCTTAAGTGAATA | 11124 |
rs375293580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50774171 | ACAACATTTGCTGTC[C/T]TTCTTCCCCCAAAAT | 11124 |
rs375295185 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50706388 | GTTATGTAAAAATTC[A/T]TTCAAAATAATTGTG | 11124 |
rs375297713 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50690603 | AAGACTGTCTCAAAA[A/C]CAAACAAACAAACAA | 11124 |
rs375305944 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50858331 | CACATGTAAAACAAA[C/T]GAATTTCAACCCATA | 11124 |
rs375322293 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50587966 | ACATTCACCAACTAC[A/C]TATTATGTCAAGGCA | 11124 |
rs375328060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551165 | GAGATTATGAGATTA[C/T]GTATAGCTATTATGT | 11124 |
rs375345248 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449489 | AACAACTTTTTCTTT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs375362345 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50669431 | TCTTAAAAATGAATA[A/G]TACCTAGAGGCATTA | 11124 |
rs375364007 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50555213 | AGGTGACAGAGCGAG[-/AC]ACACACACACATACA | 11124 |
rs375367365 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50492953 | CTGGCCTGAAGGTAA[A/T]TGTTATACTACAAAA | 11124 |
rs375390253 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50621213 | TTCTGATGTGCTCCT[C/G]AGTCACTGGGAAAAT | 11124 |
rs375406733 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679568 | CTATCCTCCTACCTG[A/G]TCCTCTCCAACCAAT | 11124 |
rs375436005 | in-del | -/TGTGTG | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460808 | CTAAGTATTTGTATA[-/TGTGTG]TGTGTGTGTGTGTGT | 11124 |
rs375442687 | in-del | -/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961046 | TTATTTATTTATTTA[-/T]TTATTTTGAGACGGA | 11124 |
rs375448287 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50760383 | AATCAACAGAACATA[C/T]ATTTTTTTCAGCACC | 11124 |
rs375448375 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50933169 | GCTCCTTGCTACTTA[C/T]GCAAATTTCTGCAGC | 11124 |
rs375449115 | snp | A/G | 1.6757e-05 | 0.00289452 | intron-variant | FAF1 | GRCh38.p7 | 1:50582714 | TCTATAGGAAAAAGT[A/G]AGTCTATTAATTAAA | 11124 |
rs375466890 | in-del | -/CT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940878 | TGTTTCTCCATCTCT[-/CT]ATTAGCCTTGGTCAA | 11124 |
rs375491882 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679723 | TAAAGCACATAGTAG[A/T]AAATATAAAATGAAA | 11124 |
rs375499054 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731947 | CAATATGATAGTGAT[C/T]CTTTGATACTGGCTT | 11124 |
rs375511902 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936249 | ATTAGTAAGAAAGAC[A/G]AACAGATATTTACAA | 11124 |
rs375520581 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50618437 | TTTTTTTTTTTTTGT[A/T]TTTTCAGTAGAGATG | 11124 |
rs375527132 | in-del | -/AGAAG | 0.00279273 | 0.0372635 | intron-variant | FAF1 | GRCh38.p7 | 1:50557703 | ACTATCAGTGTTTAT[-/AGAAG]AGGAGAAATGTGCTA | 11124 |
rs375527667 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50563512 | GAATGGCTCTGAAAT[C/T]CAACTAGATAAGGTG | 11124 |
rs375533086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766071 | CACTCCAGCCTGGGC[A/G]ACAAGAACGAAACTC | 11124 |
rs375538850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50490879 | AGCATAGGTCTCTGA[C/T]AATGTTAGGTTCCTA | 11124 |
rs375547250 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493051 | TTTTTTTTTTTTTTT[G/T]AGGGGGAGTCTTGCT | 11124 |
rs375565770 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50583874 | TATATCTGAGGGGAT[A/T]GTTTAACTCAACATA | 11124 |
rs375570512 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50655031 | GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC | 11124 |
rs375571060 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543045 | GAGAAATATAAACAG[A/C]ATATCTGATGGTTAG | 11124 |
rs375583993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512779 | CTGTGAAGAAAGTCA[A/G]TGGTAGCTAGATGGG | 11124 |
rs375592047 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50682782 | CTGCTATTTTTAGTC[C/T]TTTAATATTTAGTGT | 11124 |
rs375592266 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50582597 | GCACTTTTTAATCAG[A/G]AAAGGTCAAACTGTA | 11124 |
rs375616971 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50664226 | TGGTCTCGATCTCTT[A/C/G]ACCTCGTGATCCGCC | 11124 |
rs375635542 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50585356 | GAAGATGAGATGTAA[C/T]AATAATGTTTTACAT | 11124 |
rs375636447 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50612837 | CCTTGCTGGCTCAGC[C/T]TAGCCAAGTAATTTT | 11124 |
rs375646939 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50450717 | AAAGTATCAGAGGGG[A/G]AACTTAGGGGAATTG | 11124 |
rs375669032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50534273 | TAGCCTTGGGGTCTA[C/T]ATTATCTTCTGCTGA | 11124 |
rs375669945 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50778099 | TATAATAGAATTCTA[C/T]ATAGCAATTAGAATG | 11124 |
rs375674050 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50520721 | GGTGTGGTGGTGCAC[A/G]CCTGTAGTCCCAGCA | 11124 |
rs375682098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50852044 | TGAGCTTTCCTTATA[C/T]AGAATGGCACAACCA | 11124 |
rs375685544 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50832529 | AACATATATGAGAGT[C/T]TGACAAACACTAAAT | 11124 |
rs375687331 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50804816 | ACAGGGATAAAATTG[A/C]AAGTTTGGTTAAATA | 11124 |
rs375722133 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50473497 | TGAGATTTTCATCAC[A/C]GAACATAAAGTATGA | 11124 |
rs375728896 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50696251 | TTTACACTTTCCCAA[G/T]CAAAGGTAACTTAAT | 11124 |
rs375729019 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50923832 | AACCAGAATCATATT[G/T]TCATTTAAATAGACA | 11124 |
rs375737496 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50691956 | GCCAGGTGTGGTGGC[A/T]GACACCTGTAATCCT | 11124 |
rs375740495 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787728 | TTAGGGTATTTTTTT[-/T]AAAGCTCTTAGATGT | 11124 |
rs375746327 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50480916 | CCAAAGACTTTCCAG[A/T]GGACAAGATGTGAAT | 11124 |
rs375754453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687031 | ACAGGGTTTTGCCAT[C/G]TTGCCCAGGCTGGAC | 11124 |
rs375755252 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50592805 | ATGCCGGGCATGGTG[A/G]CACATGCCTGTAGTC | 11124 |
rs375766169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50783792 | AGGCATGAGAATCAC[C/T]TGAACCTAGGAGGCG | 11124 |
rs375779639 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50769848 | TTGGGGTCAGGAGTT[G/T]GAGACCAGCCTGGCC | 11124 |
rs375804034 | in-del | -/ATAGAAAAAAACTGGT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50483207 | GGTTTTCTATGGGAT[-/ATAGAAAAAAACTGGT]TTTTTTTGGATATAA | 11124 |
rs375805907 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819122 | GATGCTCAACCCGTA[G/T]AGAGTTCTAGAATAG | 11124 |
rs375806438 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50762689 | ATACAAAAATTAATT[A/C]CAGATGGATTAAAGA | 11124 |
rs375816493 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50490491 | AGGAAGGAAGGAAGG[-/A]AAGGAAGGAAGGAAG | 11124 |
rs375817595 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768168 | TTCAGACAAAACACA[C/T]CTTAAACCAAAAAGA | 11124 |
rs375819386 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783601 | AAAATCGGCCAGGCG[C/T]GGTGGTTCACGCCTG | 11124 |
rs375823050 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50447801 | GCTTTAGGAAATCCA[C/T]CCCTTCAGTTATAGA | 11124 |
rs375826755 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872411 | AACCTGAATAGATAC[A/G]AAGTTGCTTCTTATG | 11124 |
rs375831697 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947332 | GTGACTCAAACCCCA[A/C]CTGAAAGCCATTAAG | 11124 |
rs375834356 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50478454 | AGGTGTGAACCACTG[C/T]GCCTGGCCACAATGG | 11124 |
rs375837223 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50742860 | TATGGCCTGTGGGTC[-/A]AACCCAGCCTGCTGC | 11124 |
rs375839938 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50478912 | AAAAGTGCACAAATC[G/T]TAAGTGTACAACTTG | 11124 |
rs375844089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50925034 | AACAGAACAGAGAAC[C/G]TTGAAATTAAAAATA | 11124 |
rs375872069 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50744420 | CTCTCAAAAAAAGGG[C/T]CAAACTCCTTTAAAA | 11124 |
rs375874982 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50869189 | TATTAATATTGTCAT[C/G]TAGCTTTTCAATAAT | 11124 |
rs375875641 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466460 | GAAATGTTTGGAGTT[A/G]AGGAGAGAATTTAGA | 11124 |
rs375887522 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | FAF1 | GRCh38.p7 | 1:50490653 | CTGCCATCTCTCTCT[C/T]GTGAGCTTCCCTCTG | 11124 |
rs375890421 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50690188 | AAACTGGGTTTCAGC[A/G]TTAGCCAGGCAGGTC | 11124 |
rs375892280 | in-del | -/CA/CACACA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50819638 | ACTGACTGACTCACT[-/CA/CACACA]CACACACACACACAC | 11124 |
rs375893597 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681833 | TCTTTTGTTTTTTTT[-/T]GGTTTTTTTTCCTCT | 11124 |
rs375895388 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836164 | GTGTTTTTGTTTTTT[G/T]TTTCTGTTTTTTTTT | 11124 |
rs375909388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669205 | TATTAACAACTCTAC[A/G]GGGTTTCTCTAATCT | 11124 |
rs375911064 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50658153 | GATAGAAGAGGGAGT[A/G]TGAGGAGTCTTTAGG | 11124 |
rs375913672 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50959193 | ATACTCTGGAATATA[C/T]AGTCTTATCTGTCTC | 11124 |
rs375926769 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945181 | TACGATAAAAGGTGC[A/G]CTACTGTTAGACTGC | 11124 |
rs375929767 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50879305 | GATTAATGTAATTCA[C/T]CTATGACTGGTTACC | 11124 |
rs375930803 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50715357 | CTGTAATCCCAGCTA[C/T]TTAGGAGGCGGAGAC | 11124 |
rs375933304 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50893119 | CTTTGAGTTTCCCTC[A/G]AAGCAGCTCTTTGGA | 11124 |
rs375936233 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869892 | TAGTTCTATGATTTT[A/G]GCATCTGCTGAATGT | 11124 |
rs375948637 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50688395 | TATTTGTACACCCAT[A/G]TTTATAGCAGCATTA | 11124 |
rs375955277 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50923625 | GCAAGAACACAACAA[A/T]AAAAGAAAACTACAG | 11124 |
rs375960999 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50760690 | CACATTCAAAGCAGT[A/G]TGTAGAGGGAAATTT | 11124 |
rs375964953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461052 | GCTCACAAGAACTTA[A/G]CCCTGTATTTCCCCT | 11124 |
rs375965743 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50824487 | ACTGATTAATGCGAA[A/T]AAAAAAGGAACACTT | 11124 |
rs375978283 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931104 | ATCAATATTTAATTT[G/T]CATCCAACCTGATGG | 11124 |
rs375986456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649263 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCACA | 11124 |
rs375993876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50517845 | CCTAGTCTTATGCCT[A/G]TAATGGTCACCATTA | 11124 |
rs375998765 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742728 | GAATGAATGAATAAA[C/T]AACTACAAAAGCGAA | 11124 |
rs376001435 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928828 | CTGGCCAGGCACAGT[G/T]GCGCATGCCTGTAAT | 11124 |
rs376009675 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50630144 | TGTTCCTGTTACTAA[A/T]TATTTATTAATAAAG | 11124 |
rs376010077 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472890 | ATTTGACTTGAAAGA[C/G]AATTCAGAGAAGAAT | 11124 |
rs376012298 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50778317 | CAATAAATATTCTCT[A/G]TCTGGATCTGGGTGG | 11124 |
rs376020071 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50689155 | TAACTGAACTATACA[C/T]GTAAAAATGGTTAAA | 11124 |
rs376021571 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50903702 | CACATTAGTGATATT[C/G]TAATATACATCTGGT | 11124 |
rs376047736 | snp | C/G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50709198 | TCTCATCCTCCTTTC[C/G/T]TTTGCTCCCTTCCAA | 11124 |
rs376074043 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872900 | CGAAACTCCGTCTGG[-/A]AAAAAAAAAAAAAAT | 11124 |
rs376087364 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50689153 | TGTAACTGAACTATA[C/T]ACGTAAAAATGGTTA | 11124 |
rs376090209 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50471139 | TACATGAATTAAATG[C/T]GAATTAAACTGCTTC | 11124 |
rs376095333 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50955542 | TCTCTCCATTCAAAA[A/T]TTTGGTGGTGCAGCC | 11124 |
rs376102004 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50941367 | GGTGCCAGCCACCAC[A/G]CCCAGCTAATTTTTG | 11124 |
rs376103629 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50758331 | AATGCTGGGATTAAA[C/G]GCATAAGCCACCACG | 11124 |
rs376123152 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50774469 | TTTTCAGACTGAAAA[-/A]TGCACCTGCTAAATG | 11124 |
rs376141769 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50657054 | ATTTCTACCAAAAAA[-/A]TAACAAAATTAGCTA | 11124 |
rs376152207 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676364 | GTGAGCCAAGATCAC[A/G]CCATTGCACTCCAGC | 11124 |
rs376156889 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50685134 | GGGTAAGGCTGAGGG[A/G]GAAGAGCTGAGGGAA | 11124 |
rs376162861 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50695611 | ATCTCTTTTATAATA[C/T]ATATGATTTCTCTCT | 11124 |
rs376167918 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803049 | GACAATAGATACCAC[A/C]GAACCCTGACGACTC | 11124 |
rs376174453 | snp | A/C | 1.65206e-05 | 0.00287403 | missense | FAF1 | GRCh38.p7 | 1:50738872 | ACTTACCCAGCATGA[A/C]TAGATGATGAAGGTG | 11124 |
rs376174853 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917254 | GATACACTGCAATCA[A/T]CTATTTGCAGGCTCA | 11124 |
rs376175716 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569186 | CAAATGCCTCTATGA[A/C]ACCTTCCGTGATTCC | 11124 |
rs376198293 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50839838 | AAGAATTTCAAAAAG[C/T]TAAGGCTTTTCAAAT | 11124 |
rs376202823 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50546235 | GATACTATGTAGCCA[A/T]TAAATAGATTTCTTT | 11124 |
rs376214746 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460415 | CATAGTGCTGAAGTG[C/T]TGTCTAGTGTTCCTA | 11124 |
rs376229716 | snp | A/C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576638 | TCTCCGCACCGCCCC[A/C/G]CCCCCGCCACCACCC | 11124 |
rs376233901 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50941217 | GTTTTGTTTTGTTTT[G/T]TTTTTGGAGACAAGG | 11124 |
rs376240062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645211 | AAGTCAGTGAAAATG[C/T]CCAAAGATTGCCTGA | 11124 |
rs376247463 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50893708 | CTACCAACTATGTTC[A/G]CACAAGGTCCTATGT | 11124 |
rs376251387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50648794 | AGCTGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 11124 |
rs376251572 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50621272 | GGCTGCAAAGGGGGT[A/G]CTGTGTACACGCTCC | 11124 |
rs376267772 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50579706 | ACACAAATCCAGAAT[C/T]TGGAACCATCTACAA | 11124 |
rs376277996 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50596672 | AAGTTTAGGTTTTAT[C/G]ATAAAGGAAGCTGCC | 11124 |
rs376288347 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945266 | GCGTGGCCAGAGCCA[A/G]CTGATTGGACTAGAA | 11124 |
rs376292674 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50678907 | CCTGGCTAACATGGT[A/G]AAACCCCATCTCTAC | 11124 |
rs376302084 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449489 | AACAACTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs376316351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50733051 | CACCTCTACCCCAAC[G/T]CAGTTTCTCTATCTG | 11124 |
rs376316554 | snp | A/G | 0.000200676 | 0.0100149 | intron-variant | FAF1 | GRCh38.p7 | 1:50583765 | AAAACAAAACAAATA[A/G]ACACAAAAACAAACC | 11124 |
rs376339499 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50946786 | GGGCAACACAAAATA[C/G]ACCAAGTGATACCTG | 11124 |
rs376344207 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800686 | TCCATCCTAAATATA[C/T]GGTTTCTTATCAAGA | 11124 |
rs376354476 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50777133 | AATAAATAATATAGG[C/T]TGTCAAGTTGGCTCA | 11124 |
rs376359522 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50560589 | GTGTGCAATGCCTGA[G/T]TTAACACTTAGTAGC | 11124 |
rs376370191 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863615 | AATTCAGTATTTTAT[C/T]GAGGATTCTTGAATC | 11124 |
rs376377299 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50922759 | GGAGATGGAGGTTGC[-/A]AGTGAGCCAAGATCA | 11124 |
rs376380847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50776168 | CCAGGGATCACTTTT[C/T]GTAAACTTTTGGCTT | 11124 |
rs376390257 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50919551 | GGAGTGCAGTGGCAC[A/G]GTCTCGGCTCACTGC | 11124 |
rs376391444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50710206 | GCCTTTATGCAATTC[C/T]TTAGATATGTCTCTT | 11124 |
rs376393650 | in-del | -/GTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50941221 | GTTTTGTTTTGTTTT[-/GTTTT]TGGAGACAAGGGCTC | 11124 |
rs376397913 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874749 | TCTCCATCTTATTTT[C/T]TTTTCTTTCTTTTTT | 11124 |
rs376400714 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50731558 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT | 11124 |
rs376401315 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50665592 | AGTTACACTGGAACA[-/C]CAGCCACATCCATTT | 11124 |
rs376401693 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50826240 | CTCAAAAGTCCATAA[A/G]AAAGAATCCAGTAAA | 11124 |
rs376405032 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575673 | TGCTGTCCCAGCTGT[C/T]ATACAAAATTACTAT | 11124 |
rs376406676 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527927 | CCAGGCTGGAGTGCA[G/T]TGGTGCAATCACAGC | 11124 |
rs376419376 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869854 | CTACCTTAAAGTCTC[C/T]TTGTTACCAGTTCTC | 11124 |
rs376423932 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953505 | CACTTTGGGAAGCCA[C/T]AGTGGGTGGATCAAC | 11124 |
rs376424316 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50609092 | TAATAGTTACTGAAC[A/T]ACCACAATGTGTCAA | 11124 |
rs376434464 | in-del | -/CACACACACA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50885313 | TCTCTCTCTCTCTCT[-/CACACACACA]CACTCTCTCTCTCTC | 11124 |
rs376440808 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50580754 | TCTGTGTTAGAATAC[C/T]TTCTCTTTGCTTTTC | 11124 |
rs376457188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50765345 | CAGAGTCTCAAATTT[C/T]AACCAATACATTATC | 11124 |
rs376466118 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50665590 | AAAGTTACACTGGAA[-/C]CACAGCCACATCCAT | 11124 |
rs376474907 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519798 | TTCTTCTAGAAGATA[A/C]TTCTCCACAAGTCTA | 11124 |
rs376478110 | snp | C/T | 0.000101726 | 0.0071311 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50539662 | AAGCGGAAACTGATC[C/T]GTTTTTTGAGTCCGA | 11124 |
rs376485762 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447280 | ACAGGTGCCCGCCAC[C/T]ACGCCTGGCTCATTT | 11124 |
rs376487435 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50790979 | TTCTGTTACATAGAT[A/G]TATATGTGTGTTTGG | 11124 |
rs376488654 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701409 | AACAAACCAAAAAAA[-/A]ACACCCAATACTTTA | 11124 |
rs376492103 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858080 | ATGTAAATAGCATAA[A/C/T]ATGTAATTTAAATTC | 11124 |
rs376493368 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50638831 | AGTTTGCTTTTGCTT[C/T]GAAAAAAAACTTATT | 11124 |
rs376493567 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846660 | GAGGCGGGTATTTCC[G/T]GGTGAATTTTTATGC | 11124 |
rs376496032 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794340 | GCCAAAATTACACTG[C/T]TGTAGTACTACGACC | 11124 |
rs376496763 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803844 | TTATGTACAGCAAAC[G/T]CTGTACATAAATAAA | 11124 |
rs376500490 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50661353 | CTCAACATTTAAAAT[G/T]TTTTGAAATCTGGCC | 11124 |
rs376503401 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50608193 | GGTTGTTTAGTTGTT[C/G]ACATGGAAAGGGGCA | 11124 |
rs376504996 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50837246 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCATATGT | 11124 |
rs376510156 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50492441 | ATCTAAGTTGAAAAT[C/G]TCTTAGAATATTTTT | 11124 |
rs376516370 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50587624 | TCATAATTTTAAAAA[-/C]AGCTAAAAAATTAGT | 11124 |
rs376527083 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694969 | TGTCTCAAAAAAAAA[-/A]TTATGGCATGTATTA | 11124 |
rs376530791 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50706215 | TGTCAATTATATCAA[C/T]TCCAAATATGCTACT | 11124 |
rs376538405 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725572 | GCAATTCCCGTGCCT[C/T]AGCTATACGAGTAGC | 11124 |
rs376544722 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50549683 | GGGAGGCTGAGACAG[A/G]AGAATTGCTTGAACC | 11124 |
rs376545136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50475281 | TGGGTACATATCTGC[C/T]GGCCTGGGAAGCCAT | 11124 |
rs376546607 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50752138 | CCACACCCAGCTAAC[A/T]TTTGCATTTTTAGTA | 11124 |
rs376551626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50442244 | GGTCTTCTGAATCTG[C/T]GAGTGAGAGAAGAAA | 11124 |
rs376560175 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748304 | AGTTCGAGACCAGCC[A/T]GCCCAACATGGTGAA | 11124 |
rs376573665 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50850269 | GATTACGAAGCTATA[C/T]ATACTCCAGGAGTTA | 11124 |
rs376574210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742667 | GGGATTACAAGGGTG[A/C]GCCACTCCACCCAGC | 11124 |
rs376586002 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50764942 | TGGAAACTAGGGTGG[C/T]TCACATTCATGTGGC | 11124 |
rs376597715 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50504628 | GACAAGTACCCAACA[C/T]CAATTTCAAATGGTA | 11124 |
rs376604595 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50814857 | ACTATCACACACACA[C/T]ACACACACAAAACCA | 11124 |
rs376609836 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50842511 | TATTCTTGCCACACA[C/T]AAAATTCTTGTCTAC | 11124 |
rs376613457 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50606923 | GCTCCAGGTTTCCCA[C/T]TCAATTCCTGCGAGA | 11124 |
rs376613551 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50907585 | CTATTCAGGGATTCA[A/C]CTTCTTCCTGGTTTA | 11124 |
rs376633489 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50644016 | AAAGTCCATGTCTGC[-/C]AATTTCATTATCTAA | 11124 |
rs376643160 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50496054 | TTTAACCAAAAAAAA[-/A]GAAATTTAGATGTAA | 11124 |
rs376644823 | snp | G/T | 0.00020523 | 0.0101278 | intron-variant | FAF1 | GRCh38.p7 | 1:50857895 | AGAATTCATAAAATT[G/T]GATTACTCATCAGAG | 11124 |
rs376648071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50651031 | GGAGATGGGCAACAA[C/T]GTTGTAAATGAGTGT | 11124 |
rs376656703 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50445477 | GCTGAGAGTAGTTTC[C/T]ATATAGAGAAAGAAG | 11124 |
rs376663500 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766335 | TTACCCCCTAGAATA[A/C]TTTTTGTTTATAAAC | 11124 |
rs376676590 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739444 | TGTGTGTATATATGT[G/T]TATACACACATACAC | 11124 |
rs376686812 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766048 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 11124 |
rs376696563 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50497068 | AGAATCTTAACAAAC[A/G]TTAAGCAAAAGAAAC | 11124 |
rs376703911 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637929 | GTATATATATATATA[C/T]ACCAACACATGATCA | 11124 |
rs376714256 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449780 | GGCATGAGCCACCGC[A/G]CCTGGCCTAACTAAT | 11124 |
rs376730202 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50584203 | GTGGTCATTTTGCAC[A/G]TAGCATGTCTTGTTA | 11124 |
rs376738996 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543513 | AAAACACTTGTCTTC[C/T]TGTAAGGATGAAATA | 11124 |
rs376739579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866158 | CCAGCATTTCTCTGT[A/G]ATTAAAACCCTCAGC | 11124 |
rs376745517 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50598577 | ACACTTGCTACATAG[C/T]AGATATTCTATCAGT | 11124 |
rs376745962 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622569 | TAGTACAATTGTCAT[C/T]CAGGAATCTAATATT | 11124 |
rs376747701 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50809555 | CATACAACCTCCCAA[C/G]ATTGGATCATGAAGA | 11124 |
rs376782236 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648076 | CCAGCCTGGCCGACA[C/T]AGTGAAACCCCGTCT | 11124 |
rs376788917 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FAF1 | GRCh38.p7 | 1:50487116 | AGTAGCTATTAGATA[C/T]AGTTGGGGTTAGTAT | 11124 |
rs376790255 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50449485 | GGGGAACAACTTTTT[-/C]TTTCTTTTTTTTTTT | 11124 |
rs376791441 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656713 | CATGGCAAAACCTTG[C/T]CTCTATGAAAAATAC | 11124 |
rs376806260 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50793195 | AGTTGGTTCACAGAC[A/G]TAAAGCCCCTGGATT | 11124 |
rs376809136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50896141 | AATAGAAAAATTAGC[C/T]CAGCATGGTGGTGCA | 11124 |
rs376815196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50665092 | TCAAGTAAATTAATC[A/G]ATTTATAATTCTTTC | 11124 |
rs376816049 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50701741 | TTCAGTTCCTGAGAC[-/T]TATTCAACTCTATTG | 11124 |
rs376831884 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931068 | TTTATATTCCAGATG[C/T]TTCTCTTATACGAAA | 11124 |
rs376836344 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50728409 | GCGATAAAAGACGAA[G/T]TTAGAGAGAAAGACA | 11124 |
rs376855014 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50553611 | GTGCACAGCACCAGA[C/T]AAACCTCCTCTAGAG | 11124 |
rs376855065 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50514156 | GAATGATATTTACCT[-/C]CCAGCCTTATATTAT | 11124 |
rs376855534 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958976 | GTCTTTCACAATGCA[C/T]ACAGTTCTACTTTCA | 11124 |
rs376874167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860966 | AGCCATAATCCTAAG[C/T]GAATTAATGCAGAAA | 11124 |
rs376874969 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50666002 | GCCAACATGGTGAAA[A/C]CCTGTCTCCACTAAA | 11124 |
rs376879025 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50518569 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGG | 11124 |
rs376883390 | in-del | -/TCAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674371 | CAAAGAAATTGTTAC[-/TCAC]ACTATTCACTTACTT | 11124 |
rs376890368 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50535423 | CTCCATTGCAGCCAT[A/G]AGTCTCATCATTAAC | 11124 |
rs376893269 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50511814 | AGATCCTTGAGGAAT[C/T]GCCACACTGTCTTCC | 11124 |
rs376899185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50915699 | GTGAAGCAACTAACC[G/T]TCCTCTTAACCTTCT | 11124 |
rs376905414 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50668847 | GATCAGGAAAAAAAA[-/A]TTTAACCACATGATT | 11124 |
rs376914699 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50508867 | ACCACACCCTGCTAA[-/A]TTTTTTTTGCATTTT | 11124 |
rs376925566 | in-del | -/CTAGAAC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50727354 | TTATATCCCTAGCAC[-/CTAGAAC]AAAGACTTAACACAT | 11124 |
rs376931518 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50604071 | TACCATGTAAGCAAC[C/T]GGAGCTGGAAGAAAC | 11124 |
rs376937412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50929188 | AATGATGTGTTTAAT[A/G]ATACTCTCAAAGTAT | 11124 |
rs376940238 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461178 | TCTAAAACCAATAGC[C/T]CCCCACAGCCTATAG | 11124 |
rs376943077 | in-del | -/TACCTAAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50834894 | ACGGCAAAGAAAAAA[-/TACCTAAT]ACAGCCAGTGAAGGC | 11124 |
rs376945233 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50795921 | ACTATGGACTATGAC[C/T]GGAGCCCAGGAGATT | 11124 |
rs376946668 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50442875 | CCTGGAATCCTCTCC[G/T]CTTATAAGGAACTCA | 11124 |
rs376947759 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50657786 | AATAAAACAAAAACA[C/G]AGAACTCACTCTATT | 11124 |
rs376962282 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475670 | CTTGCTCTAAGGACA[A/G]CCGGATGGCCTAGGG | 11124 |
rs376971542 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947193 | CAACCACTACTTCCC[C/T]TAGGGAAAAAGAGGA | 11124 |
rs376972312 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649856 | TGTAGTCCTAGCTAC[A/G/T]CGGGAGGCTGAGGAG | 11124 |
rs376973652 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50953735 | CAAAAGCGAAACTCT[G/T]TCTCAAACAAAAAAA | 11124 |
rs376975855 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638760 | AGCTATTGCTTTTTC[-/AT]AGAGTCCTTCTATCA | 11124 |
rs376981584 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704890 | AGAAACAGTTCATAT[A/G]TTTCTGAAAGAAAAC | 11124 |
rs376987736 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928866 | CTTTGGGAGGCTAAG[C/T]TGAGCTCAGGGGATC | 11124 |
rs376989422 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684473 | GTTCCTATCACAGTC[A/G]AGGCATTCAGGCAGA | 11124 |
rs377008377 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50526430 | GCGAGACCCCATCTC[C/T]ATTAAAAATAATAAT | 11124 |
rs377022777 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950712 | ACACCTGTGAACACA[A/G]AAGCATGGCACTAAA | 11124 |
rs377030108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834519 | GGATGAGATAATTGA[A/G]GCCAAGAGACCAAGG | 11124 |
rs377043460 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50691512 | CTCCCAAAGTACTGG[A/G]ATTACCGGCATGAAC | 11124 |
rs377053518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50715722 | TTATCAGGAACAGAG[A/G]GGTTACCTGTAAAAT | 11124 |
rs377069093 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575206 | AGCCACTGCGCCCAG[A/C]CAAATGGCAGTGTAT | 11124 |
rs377071563 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50891524 | TTTGATGATAGTGAC[A/G]TACAGATGAGGTTTT | 11124 |
rs377079957 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50903515 | TGATGTATCTTTAGT[A/G]TATGTATAAATTAAA | 11124 |
rs377082283 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619095 | CTGCGTGGTAGATCT[C/T]TCTCCATCCCTTTAC | 11124 |
rs377085323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603419 | ACATCACATTTCCAA[C/T]GTAGATAAGGTTTTT | 11124 |
rs377089710 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50659830 | AGTTTAATTTCTTCC[A/G]TATCGTTTCAGATAA | 11124 |
rs377098040 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50626739 | TATTCTGATATAGTA[C/T]GGAGAGTTGATTGAG | 11124 |
rs377104862 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789732 | TCATATCATTCTCTT[C/T]CTCAACCCTACTCTC | 11124 |
rs377116003 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50574108 | TCCATCCTGGGCAAC[A/G]GGGCGAGACTCTGTC | 11124 |
rs377120612 | in-del | -/AATT | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50897153 | AAGTCTAATGAAATA[-/AATT]AAAGAATATATAAAT | 11124 |
rs377126826 | in-del | -/TG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50851052 | TGCATCTGATTGATA[-/TG]AACAATCCTAAAAAT | 11124 |
rs377127369 | snp | A/G | 1.66621e-05 | 0.00288631 | synonymous-codon, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50857941 | TACCACTAAGTCCCA[A/G]TTATTTTGTTCAAGC | 11124 |
rs377131911 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499796 | GGAGTGGAGAAAGAA[C/G]AAAGAAATTTGTTAC | 11124 |
rs377142113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684708 | TTTTGCACTAAGCTC[C/G]AGCATTCAACTAATA | 11124 |
rs377157617 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591216 | CTGTAAATGTGCTGT[A/G]TTACATTGAGGATTC | 11124 |
rs377169303 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50848992 | AGCCAGGCGCAGTGG[C/T]TCATGCCTATAATCC | 11124 |
rs377172172 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50872616 | AATGCTATCAAACAG[A/G]CTGGGCGCGGTGGCT | 11124 |
rs377182550 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50890438 | TTGCTCGTTAGTTGA[C/T]GCAGTTTCTTCCTAG | 11124 |
rs377194410 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947605 | AATGAAATTATAATC[A/G]GGAAGAGTGAATAAA | 11124 |
rs377213896 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847419 | ACTATGCCTGAAATT[-/A]AAAAAAAAAAAAAAA | 11124 |
rs377228131 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50613335 | AGACTTAAAACTACC[A/C]ATCAAAATATGCAAA | 11124 |
rs377234558 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863314 | AAAATTATTTGAACT[G/T]AACAATAATAATGGC | 11124 |
rs377238394 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50702036 | CTTATTGTTATTCTG[A/G]GTCATGTGTATATTC | 11124 |
rs377238427 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50595937 | TGAAACTAACAGAGC[A/G]AGAAGGAGCACATTA | 11124 |
rs377240484 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894796 | AACAAATTAAGGAAG[A/C]ACTTGAAAAACTAAC | 11124 |
rs377257684 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50760810 | AACACATTCAAAAGC[C/T]AGCAGAAGGCAAGAA | 11124 |
rs377258727 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50518481 | AGTCTCACTCTGTTG[A/C]CCAGGCTGGAGTGCA | 11124 |
rs377264598 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50856359 | CTCAAGACAAGAAAC[G/T]TGGGAGCATCGTTTC | 11124 |
rs377267224 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50924915 | TTGAACCCAGGAGGC[A/G]GAGGCTGCAGTGAGC | 11124 |
rs377267905 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50799003 | TTTTAGTAGAGACAG[A/G]GTTTTACCATGTTGG | 11124 |
rs377267981 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50489770 | GAGCTCAATGCAAGA[C/T]GTTACAAAAGTAACT | 11124 |
rs377269124 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50625945 | AAACAGGGAAATCAG[A/G]AGAAAGTTATAAGAG | 11124 |
rs377270550 | snp | C/G | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50692243 | CTTGAAGTATTTACT[C/G]TGTGTGTGTGTGTGT | 11124 |
rs377276016 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874439 | TGATCACAGCTCACT[A/G]TAATACTGAACTCCT | 11124 |
rs377280198 | in-del | -/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50663998 | TGAAAATCTGTTAAT[-/C]TTTTTTTTTTTTTTT | 11124 |
rs377290445 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50548180 | CAAATATATGACGAG[A/G]TAAGACATGGTTTTT | 11124 |
rs377300593 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803083 | AGGCTTGTAAATCCT[C/T]TGAGTAAAGCAAATG | 11124 |
rs377319109 | snp | C/T | 6.965e-05 | 0.00590086 | intron-variant | FAF1 | GRCh38.p7 | 1:50567051 | TAATAGAAGCCCAAC[C/T]TGTAACTTGTGAACA | 11124 |
rs377342290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50706926 | TTAGACAGATAGGAC[A/G]GGCACGGTGGCTCAC | 11124 |
rs377344061 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50910426 | GCTGTCAGACAGGGA[A/T]GTTTAAGTCTGCAGA | 11124 |
rs377365751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932388 | CCATTCTACATGGGA[A/G]AAATTAGCCAAAACA | 11124 |
rs377374794 | snp | A/G | 0.000131796 | 0.00811668 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50655493 | TAATTGGTGGCGAAC[A/G]GGGATACTTGTAAGG | 11124 |
rs377386079 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490490 | AGGAAGGAAGGAAGG[-/A]AAAGGAAGGAAGGAA | 11124 |
rs377401572 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591037 | TTGTTCCTGATTTTA[A/G]AGAAAAAGTTTTCAG | 11124 |
rs377412135 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894840 | AATAAAAACACAGCA[C/T]GCCATGCCAAAACCT | 11124 |
rs377425483 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662924 | GGATGGTCTCCATCT[C/G]CTGACCTCGTGATCC | 11124 |
rs377425819 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50651182 | AAGGTTAATGAGAAG[A/T]ATACTGAACAAAACA | 11124 |
rs377430543 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601575 | TACTCTCAGGCACTC[A/G]GGAGGCTGAGGCAGG | 11124 |
rs377432765 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637022 | ATGGATCTATTCCTG[A/C]ACACTCTATTTTACC | 11124 |
rs377440559 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50868224 | CTACACATTGTGTAC[A/G]GTACACAGTGCTTGG | 11124 |
rs377442041 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50671732 | TACTGAACATTTTAA[-/T]TTTTTTTTTTTTTTT | 11124 |
rs377450384 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50585902 | AAAAAAAAAAAAAAA[-/G]AAAAAAGTCTGGCAT | 11124 |
rs377458659 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50508571 | AGTGTTGTCAGGGGC[C/T]ATGTGTAAGTGTGTG | 11124 |
rs377459611 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50724306 | ACACATACACACACA[C/T]ACACACACACACACA | 11124 |
rs377462846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50530508 | GGAAGGGTGGTGGGG[A/G]GAGGTGGGGATGTTT | 11124 |
rs377526690 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490498 | AAGGAAGGAAAGGAA[A/G]GAAGGAAGGAAGGAA | 11124 |
rs377527725 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50586447 | GTGTCAAATGTCAGC[A/C]TTTCCTCCTTGGGCA | 11124 |
rs377531239 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50599835 | GTATTTAGACAAGTA[C/T]CCCTTATTTAAAATG | 11124 |
rs377534240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50924721 | GGCACAGTGGCTCAC[A/G]CCTGTAAACCCAGCA | 11124 |
rs377535263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50619279 | TGATCCTGTCATTGT[A/G]GTGTTAGCTGGCTGC | 11124 |
rs377547832 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50628365 | ACACAGCTATCTGAT[C/T]TGAAACTGTAGGATT | 11124 |
rs377550460 | in-del | -/GA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50517101 | GATTTATGAAAAAGA[-/GA]ATTTAAGGCAGTATT | 11124 |
rs377564272 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50804783 | CACAGGAAAGAGAGA[A/C]AAAAAAAGCCACAAG | 11124 |
rs377568429 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50782495 | AACATTTGTACAACT[A/G]TACAATGTGTGTTCT | 11124 |
rs377584168 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739288 | TGCATACATATACAT[A/G]TGTACATGTGTACAC | 11124 |
rs377588215 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812802 | CACTATTCACCATAG[C/T]AAAGACATGGAATCA | 11124 |
rs377589218 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554626 | CTTCACTACACCCCA[C/T]TAAAATCACTCTGAT | 11124 |
rs377591794 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50844326 | CCATTCTACAGGCTG[C/T]CAATCACAACTGATT | 11124 |
rs377598439 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50612277 | ATTCTACAATCACAA[C/T]AAATTCAGAGAATCA | 11124 |
rs377603121 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50590753 | TTGGGAGGCTGAGGC[A/G]GATAGATCACCTGAG | 11124 |
rs377603569 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767606 | CCCACAGACTAACAG[C/T]GTACCTTTTGGCAGA | 11124 |
rs377603958 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50742920 | TGGTTTTCACTTTTT[C/T]TAAAGGTTGGAAAAT | 11124 |
rs377622382 | in-del | -/CC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50485697 | AAAAAAAAAAAAAAA[-/CC]AAAAAAACAAAAAAA | 11124 |
rs377622865 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590710 | TTCTTGGCCGGGCGC[C/T]GTGGCTCACGCCTGT | 11124 |
rs377624455 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50721883 | CCACCTTAGCCTCCC[-/A]AAAGTGTTGAGATTA | 11124 |
rs377635290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756574 | TTCAGGTATCTTTTC[A/G]GCAGTGCCCCACTCT | 11124 |
rs377640909 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794279 | GAGGAAAAAAAAATT[G/T]GGACTGGGAAGAGAA | 11124 |
rs377642151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50847056 | ATCTGTGATACAAGC[A/G]GATCATTCTTGATTT | 11124 |
rs377642651 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869919 | ATGTGATTGTGGCTT[C/T]TCCTGTGGTATATAA | 11124 |
rs377642744 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50488031 | TTTAAAAAAGGGGCA[A/G]ATAAGTTTGGATAAG | 11124 |
rs377646049 | snp | C/T | | | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440774 | GCTTGAACAGTTTCC[C/T]TATGCTGCAATGGAA | 11124 |
rs377665958 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927655 | ATGCTGAAAGGTGAG[C/G]GGTAATTGAATGGAA | 11124 |
rs377674269 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50586671 | AGTTTGTTCGTAGAT[A/C]TAAGATCTCCTGGTT | 11124 |
rs377691432 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50796162 | CTCACAGTATCAACT[A/G]TGGCCTTATGACCAG | 11124 |
rs377699071 | snp | A/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462653 | GAATCTGGGGCAAAT[A/T]TGCATTGAACACGCT | 11124 |
rs377702344 | snp | C/T | 4.99921e-05 | 0.00499935 | intron-variant | FAF1 | GRCh38.p7 | 1:50583615 | CACAGTAGCATAAAA[C/T]AGCATCAAATTTATA | 11124 |
rs377714617 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50934688 | ATGTTCACACCACTG[C/T]ACTCCAGCCTGGGTG | 11124 |
rs377727552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50719227 | ACTAGGTTTTGCTCC[C/T]GTCCAGCTAAACTAA | 11124 |
rs377732241 | snp | C/T | 6.59478e-05 | 0.00574191 | intron-variant | FAF1 | GRCh38.p7 | 1:50655414 | AGAGAAAGGAGGATA[C/T]AAAACTGAAAATTTG | 11124 |
rs377733380 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50691668 | GCGATCTCGGCTTAC[A/G]CAACCTCCACCTCCC | 11124 |
rs386366932 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50701404 | AAACAAACAAACCAA[-/A]AAAAAACACCCAATA | 11124 |
rs386631100 | multinucleotide-polymorphism | CAG/TAT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50582286 | GCCTTCTGCAAGAGC[CAG/TAT]CAGTACCCCTATCAC | 11124 |
rs386631101 | in-del | GGTGACAA/TC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717403 | AGGACACAATGAGAA[GGTGACAA/TC]AGCCAGGATGAGGGA | 11124 |
rs386631102 | multinucleotide-polymorphism | AC/GA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50741887 | ATAAGATATACAAGT[AC/GA]AAAAGTCAATTACCA | 11124 |
rs386631103 | in-del | AAG/CTTGCC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50758288 | CAAACTCCTGACCTC[AAG/CTTGCC]TGATCCACCTGCCTC | 11124 |
rs386631104 | in-del | ACC/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50763867 | ATAAACTTTTAAGAA[ACC/T]ACCATTTCCCAAATT | 11124 |
rs386631105 | multinucleotide-polymorphism | AGC/CAG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50832349 | TGTCCAGTACTGGCA[AGC/CAG]AATCCAGCAGTAGCA | 11124 |
rs386631106 | in-del | GA/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50862235 | GGCCCATTCAAGAGA[GA/T]AATTAACAGAAGCTG | 11124 |
rs386631107 | multinucleotide-polymorphism | AG/TA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50899324 | TGACCTTCTATCATC[AG/TA]TATCATTTCTAGGTC | 11124 |
rs386631108 | in-del | A/GC | | | intron-variant | FAF1 | GRCh38.p7 | 1:50919311 | ATACTAGATGGAACT[A/GC]TAATCTACACAAAGA | 11124 |
rs397700447 | in-del | -/A | 0.375 | 0.216506 | intron-variant | FAF1 | GRCh38.p7 | 1:50510184 | AAAAAAAAAAAAAAA[-/A]TTTAAATTTAAAACT | 11124 |
rs397703323 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50489910 | aaatatttgttggca[-/A]caaaaGGCAAAGATT | 11124 |
rs397709840 | in-del | -/TA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637928 | GTATATATATATATA[-/TA]CACCAACACATGATC | 11124 |
rs397734559 | in-del | -/GTAA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642743 | TTCCTTTTAATGTAA[-/GTAA]TTCATACTTACTGTA | 11124 |
rs397735916 | in-del | -/TA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50694008 | GTGTCATTATATATA[-/TA]CATGACATATATGAC | 11124 |
rs397761119 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50929108 | GAAAAGAAAAAAAAA[-/A]CTGGGAAGGCTAGCA | 11124 |
rs397783600 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50947189 | ATTCAACCACTACTT[-/T]CCCTTAGGGAAAAAG | 11124 |
rs397793458 | in-del | -/T | 0.5 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50547074 | CGTATTTTTTTTTTT[-/T]GTAGAGATGGGTTTC | 11124 |
rs397860409 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50637295 | AAAAAAAAAAAAAAA[-/A]TACAAAAATTAGCCA | 11124 |
rs397861490 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50538571 | AAAAAAAAAAAAAAA[-/A]GTCTTATTACAGTTA | 11124 |
rs397862445 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707220 | AAAAAAAAAAAAAAA[-/A]GAATTAGGCAGATAA | 11124 |
rs397862672 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50538571 | AAAAAAAAAAAAAAA[-/A]GTCTTATTACAGTTA | 11124 |
rs397862723 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50597146 | TGCCTAGCACACAGT[-/T]GGTGGCTCAACAAAC | 11124 |
rs397862883 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576846 | TCTTTTTTTTTTTTT[-/T]GTAGAGATGGTGATC | 11124 |
rs397863480 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50708533 | AGTCAAAAAAAAAAA[-/A]TGTCATGTAGAGTTG | 11124 |
rs397864080 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458989 | TTCTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT | 11124 |
rs397864101 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748493 | TGAAACTCTGTCTCA[-/A]AAAAAAAAAAAAAGA | 11124 |
rs397956898 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679332 | AAGTACAAAAAAAAA[-/A]GAATAGCATTTCATT | 11124 |
rs397959024 | in-del | -/GT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50820866 | TGTGTGTGTGTGTGT[-/GT]ACACATACCAGATTT | 11124 |
rs397969063 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674271 | CAATTTTTTTTTTTT[-/T]ATTGTACCATGACAC | 11124 |
rs397976873 | in-del | -/CACACA | | | intron-variant | FAF1 | GRCh38.p7 | 1:50780022 | ACACACACACACACA[-/CACACA]GAGGAAGTAAAAGAG | 11124 |
rs397980161 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50748506 | TCTTTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG | 11124 |
rs397980162 | in-del | -/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50924294 | GGGATTGGTTTCTTG[-/T]TTTTTTTTTTTCAAA | 11124 |
rs397980163 | in-del | -/A | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50954560 | GCGTAAGACTCTCTC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs527240377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691752 | TGCACCACCACGCCC[A/G]GCTAATTTTGTATTT | 11124 |
rs527241011 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638666 | GGCCAGGTTGGTGTT[A/C/G]AACTCCTGACATTGT | 11124 |
rs527245629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588001 | GTTAAAAACTAGGTA[C/T]GTCAGCCAGGCATGG | 11124 |
rs527253893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793325 | GTATCTGTGTGCCAA[C/T]AAAAAGAAAATATCC | 11124 |
rs527257473 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447167 | GTCTCCCTCTGTTGT[C/T]CAGGCTGGAGTGCAG | 11124 |
rs527257481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50538668 | GAGAAACACTAGTTC[C/T]TGCAACATTGCCTCT | 11124 |
rs527264124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50942493 | GGGAAGGGAAGGGAA[A/T]TAAATGTTCAGTAAA | 11124 |
rs527279491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50641703 | TTAGGCAAAGTTGAT[G/T]AATCATGTTGGCCAA | 11124 |
rs527280781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579027 | TGGTTACAAATCTAA[C/T]AGGAAGCAAAATATT | 11124 |
rs527283559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50480415 | GGTTTCTATGAGTAT[A/G]TATAAATAACGGTTT | 11124 |
rs527284954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588232 | ATGGAAGTTGCAGTA[A/C]GTGCCACTACATCCA | 11124 |
rs527288971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648931 | AACTCCATCTCAAAA[A/G]TTAGGGGGCCTGGCC | 11124 |
rs527303485 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50671045 | ATAATACCTTATTTG[-/A]AAAAAAAAGGAAATA | 11124 |
rs527304579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892047 | TTTACCTACTCAAGC[C/T]TCAGCAATGGTGGAT | 11124 |
rs527313581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479613 | TCCCTTTAATCCACC[G/T]GTCTGCTTGCTTTCT | 11124 |
rs527315057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50934364 | CTACAACCCAAAGAA[A/T]TTTCTTTATAATTTC | 11124 |
rs527316098 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50633365 | TAATTAATTCCATCT[A/C]CTTGCACTTTGAAAT | 11124 |
rs527320637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846624 | CTTGTAAGATCTCCA[C/T]CCACAATCAGTGGCA | 11124 |
rs527324936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50839099 | GAGAAGTTTTCTTCA[A/T]AAAAATAAATATATG | 11124 |
rs527325145 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50489923 | GCACAAAAGGCAAAG[A/C]TTATAGAAAATCATG | 11124 |
rs527325202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50642253 | CTTTTCTGATGTCAC[A/G]GTCATCCCAAATTTC | 11124 |
rs527325654 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602964 | TCTCACAATAACTCT[G/T]CCAGGTAAGGATTAT | 11124 |
rs527332282 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50646396 | TCAAAATGTTTATCC[-/A]AATTACTATACTCAT | 11124 |
rs527338862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461906 | AAGAAAAAAAAAAGA[C/G]GAAGGAGGGAATGGG | 11124 |
rs527342564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579813 | ATTTAAGATATCTAA[C/T]ACTCAAATATAACTT | 11124 |
rs527348045 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50887318 | AAATTTTCTCCCATT[C/T]GGTAGGTTGCCTGTT | 11124 |
rs527378048 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521714 | AATGAATGCTTTTAC[A/C]GTAATAAATGGTGAC | 11124 |
rs527382434 | snp | C/G | 0.00518234 | 0.0506391 | intron-variant | FAF1 | GRCh38.p7 | 1:50447194 | GCAGGGGCACGATCT[C/G]GGCTCACTGCAAGCT | 11124 |
rs527401506 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50669981 | ACAAAATAAGCCAGG[C/T]GTGGTGGCGCATGCC | 11124 |
rs527408152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50927037 | CACTAAATAATTCCA[C/G]GTCTATAAGTACTCA | 11124 |
rs527415908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521070 | TGACAAAAATTGTAT[A/G]TATCATGTATAATCT | 11124 |
rs527421052 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50845166 | TCTCTCCTTTAAAGT[-/AA]AAGCATGATATTAAC | 11124 |
rs527423420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50887691 | TCAGATGGTTGTAGA[C/T]GTGTGGCATTATTTT | 11124 |
rs527426325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50530253 | GGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 11124 |
rs527427808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50776832 | CCCAACTAATAAACC[C/T]GAGATGCCTTAGCAA | 11124 |
rs527429766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50785724 | TAGCTGCTATAGGAA[A/G]CAGTATGGAAGTTCC | 11124 |
rs527436973 | in-del | -/TT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50493034 | AAAGGATTAAACTTC[-/TT]TTTTTTTTTTTTTTT | 11124 |
rs527437311 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50759837 | TGACTTTTTAATGAT[A/C]GTCATTCTAACTGGT | 11124 |
rs527438250 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936207 | AAAACAAGTAACATA[C/T]ACTTCCTGGCTGTAA | 11124 |
rs527443062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880479 | TGAGGTCACAAGGAC[A/G]GGGCACTGATCCAAC | 11124 |
rs527450529 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50943001 | AGTCTGGTAGCAATA[C/T]AACATCCTTGAGAAG | 11124 |
rs527450960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602268 | AAACCATATCTCAAG[C/T]TTGTCATCGTCCTCA | 11124 |
rs527467314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545110 | TCTGAATTCCAAACC[A/G]CAAAAAAGAGGCTAA | 11124 |
rs527471445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50654553 | GAAATCATTATAAAA[C/T]ATATAATAAGGGTAA | 11124 |
rs527472194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862387 | TCAAAAATAGAGAAC[A/G]CTGGATAGAGAGCAA | 11124 |
rs527488648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452976 | CCACTAGTGAGAGTT[C/G]AACAAAATGTCTGAT | 11124 |
rs527489501 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50946322 | AAAATATCCTCCCCA[A/C]CCAAAGGAGAGTTGG | 11124 |
rs527491802 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739305 | GTACATGTGTACACG[C/T]ACATGCATATACATG | 11124 |
rs527492115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50954834 | AGGTGTGAGCCACCA[C/T]GCCTGGCTTAAACAT | 11124 |
rs527493296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551910 | TAGATAAATGCACTG[A/G]GCACTTACTCTGTAC | 11124 |
rs527499158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50444514 | AAATAAAATCACAGG[C/G]AAGCAGAACCCAGCT | 11124 |
rs527501483 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50918167 | ACATTTCACTGAATG[C/T]AAATTTCTTTTTTTT | 11124 |
rs527505178 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50655177 | GAGGCGGCCGCCACC[A/G]TGCCCAGCTAATTTT | 11124 |
rs527511064 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50706462 | GAAATCATAGCAACA[C/T]TTTGTAAAGCCTATA | 11124 |
rs527518131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807886 | TGCTAAACATGCCAA[A/C]ATTCAAATTCAGGAA | 11124 |
rs527520052 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50443288 | ACCATGCTGGGGTTG[C/T]CATATGCAAGATTAG | 11124 |
rs527540233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955616 | AGAATGACTATGTGA[C/T]CCAGCAATTTAACTT | 11124 |
rs527540626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50505075 | GAATATTTTGATTAA[C/G]GTAATATATCTAACA | 11124 |
rs527555352 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768093 | GCTAAAAGTAAAGGG[A/G]CAGAGAAAAATCTAC | 11124 |
rs527556929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488982 | TTGACATGAATAAAC[A/T]TTGATTTCCAAACAG | 11124 |
rs527569399 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50719680 | CACAATTCTAACCAT[C/T]TAGACAAAATTTGAA | 11124 |
rs527570597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50898365 | AGGAGTACTATGCAG[C/G]TATAAAAGAAATAAG | 11124 |
rs527590030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50799613 | TGTATCAGTGAGGTG[C/G]GTATTTATTTCCTAC | 11124 |
rs527591849 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50700947 | AAGAATCACAGGAAA[A/C]CTCAATATTTATAAA | 11124 |
rs527597371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50853963 | ATACTTCATATATCA[C/T]GGAAGCTTGAGTATA | 11124 |
rs527602459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50792525 | AAATGAAAACTCTCA[A/G]AAGAGTCCACATTTC | 11124 |
rs527606639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846543 | CTTTGAAACATACGA[C/T]AGAGGTTCTGATGGA | 11124 |
rs527606797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50899402 | TCTTACATGCTTGGT[A/T]ATTTTTGATTGGGTC | 11124 |
rs527608049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949578 | ATATTTTAGGCTTTG[A/C]AGGACATGCAGTCAA | 11124 |
rs527613186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753909 | ATTACAGGGGTACGC[C/T]ACCATGCTCAGCTAA | 11124 |
rs527626683 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50690953 | TATTCCATTGTATGG[A/T]TATACCACATTTTGT | 11124 |
rs527639756 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50749783 | GACAGAGTGAGAACC[C/T]GTCTCAGAGAAAAAA | 11124 |
rs527642886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50913720 | AGAATTTGTCTATTA[A/C]TTTCCAAAAGACTAA | 11124 |
rs527644817 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50555928 | TATATATAAAATTAG[C/G]TGTGTGTATATATAC | 11124 |
rs527653614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50906817 | ATACACAATCATGTC[A/G]TCTGCAAACAGGGAC | 11124 |
rs527663614 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50657005 | CACTTGAGCTCAGGA[C/G]TTCAAGATGAGCCTG | 11124 |
rs527669532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50766041 | AGGGTGCAGTGAGCC[A/G]AGATCGCGCCATTGC | 11124 |
rs527672469 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50801013 | AGACAAAAGTTATGA[A/T]TTTATTTTTAACTCA | 11124 |
rs527678560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50754724 | TGATAAAGATATACC[C/T]GAGATTGGGCAATTT | 11124 |
rs527679504 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50761400 | AAAAAGAGAATTTTA[A/G]ACCAATATCCTTGAT | 11124 |
rs527681260 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50558251 | TTTTAGAATAAGATA[C/T]TTATCTTATTTTTGG | 11124 |
rs527683626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855033 | AATCCTCGATTGAAC[A/G]TTTTGGATTTTAGAT | 11124 |
rs527686067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50907338 | ATATTAGTCTAAAAT[C/T]CTCTTTTTTGGTTGT | 11124 |
rs527689349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50554858 | GATCTAGAAATGTTA[C/T]ACTACTTGTCTAATA | 11124 |
rs527692688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748165 | TAGTTGGTCTGCAAA[A/G]GACAGACAAACCAAA | 11124 |
rs527699483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657636 | TTATGTTTTAAAAAT[A/G]CAGAAGCCTAAAGTA | 11124 |
rs527710867 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50792760 | TGGTGACTGTTTTCT[G/T]TGAGTTGGGAATGAC | 11124 |
rs527712324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810242 | CCTGGGCAACAAGAG[C/T]GAGACTCTGTCTCAA | 11124 |
rs527720084 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50710815 | CACCATGTTAGCCAG[C/G]ATGGTCTCAATTTCC | 11124 |
rs527724823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951083 | TAAAAATATTTAAAA[A/G]GTTAGCTGGATGTGG | 11124 |
rs527736186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650379 | TTGGGAGGCCGAGGT[A/G]AGGATCACTTGAGGC | 11124 |
rs527747472 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50834618 | CCCCTAATTACTATT[C/T]CAATACTCAGGATGA | 11124 |
rs527753625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50748873 | AGAGTGGGGGGAGAA[C/T]TTAAGATACACAAGT | 11124 |
rs527756774 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50593840 | TTTAAGTGATATAAA[C/T]ACGTATTCAAAGGAT | 11124 |
rs527759962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50482051 | TATCCTTTTAAATGT[A/T]CAGTTCTGTGAGTTT | 11124 |
rs527762471 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510571 | CTCAAGTCAGTCCCT[A/G]TGTGTCAGGGCTCTG | 11124 |
rs527779489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50901883 | AACAACAACAACAAA[A/C]CCTGTTACAGCCAGT | 11124 |
rs527780115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606071 | AAATATGTAGCATAG[C/T]GGACTAGATTTTCAA | 11124 |
rs527781185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944195 | CTGTTTCCAGTAGAC[C/T]TCCCAGTAAGTTTAC | 11124 |
rs527794851 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50490489 | GAAGGAAGGAAGGAA[A/G]GAAAGGAAGGAAGGA | 11124 |
rs527795425 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | FAF1 | GRCh38.p7 | 1:50694011 | TCATTATATATATAC[A/G]TGACATATATGACAT | 11124 |
rs527806154 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50951714 | GGACAGAGGAGAAAG[C/G]AAAGAAAGGACAGGT | 11124 |
rs527806906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848455 | GTATAATTATGTCAA[C/T]GGAGAATAAAAAATT | 11124 |
rs527808210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50902705 | TTTGCATATAACTTA[C/T]GCACATCCTCCAGTA | 11124 |
rs527814024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50547813 | AATAACAAGGGTATA[C/G]CTAATCTATAGGAGA | 11124 |
rs527819238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50539913 | CAGAAGTGATTATCA[A/T]ATAGAAAAGCAGGAA | 11124 |
rs527821863 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768904 | AACAAGAAGAAACCA[A/C]TTACAAAGTTAGGAG | 11124 |
rs527827426 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50481793 | TGGATATTTAGATCT[A/G]AAAGAAGTATATTAT | 11124 |
rs527830960 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50797431 | GAATGCCAGGTGTAG[C/T]GGCTCATGCCTGTAA | 11124 |
rs527833818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50522210 | ATCCTACCTAATCTT[A/G]GTAAGAGCACTGATT | 11124 |
rs527836634 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50839337 | TCCAAGTTCACATAC[C/T]CCCGCTAAAAATTCA | 11124 |
rs527837827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515421 | AGAAATCACTTGTTA[G/T]ACAGGAAATTTGTGA | 11124 |
rs527847453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671768 | AGAATCTTACTCTGT[C/T]GCCCAGGCTGGAGTG | 11124 |
rs527869520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463588 | CTCTTAGCCCCAGTT[A/G]TCTAACCTGTAAAAT | 11124 |
rs527871613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453919 | TGGGGAACTGCAAAC[C/T]TGCCTCCTGACCCTA | 11124 |
rs527873027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881073 | TCAAACATTAGTACT[A/G]TTTAAAAAGCTCCCC | 11124 |
rs527873293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562436 | ACCCTTTGTTCCCCA[A/T]ACGTAATTATGAGGC | 11124 |
rs527873597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723923 | CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 11124 |
rs527901335 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50508865 | CCACCACACCCTGCT[-/A]AATTTTTTTTGCATT | 11124 |
rs527905646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50769117 | ATGACAAAGGGGACA[C/T]TACCACCAAACCCAC | 11124 |
rs527908061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50571872 | CTAAGGAAATATTTG[C/T]TGATGAACTAAAAAG | 11124 |
rs527919767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626742 | TCTGATATAGTACGG[A/G]GAGTTGATTGAGGGG | 11124 |
rs527928271 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50631482 | CTTGTGTTTAAGTTA[C/T]CCTTATTTTACTTAA | 11124 |
rs527939944 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50714169 | TCACTGGTATAAATA[-/T]TTTTTTTCTTCATTA | 11124 |
rs527952707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50717419 | GTGACAAAGCCAGGA[C/T]GAGGGACTGATTTTG | 11124 |
rs527954001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619977 | GCAATGGCACAATCT[C/G]GGCTCACTGCAACCT | 11124 |
rs527954641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912749 | CAGTGTAGGTGCATG[C/T]ACATTTTGTCAAACA | 11124 |
rs527956370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50921320 | CACTATCAGTGGCTG[C/T]GTGCACCATCCAAGA | 11124 |
rs527965007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872078 | TCAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 11124 |
rs527973415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497618 | CAGTGGTGTGATCTC[A/G]GCTCATTGCAACCTC | 11124 |
rs527987335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872776 | GTGGTGGTGGGTGCC[C/T]GTAATCCCAGCTACT | 11124 |
rs527997439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50817995 | AAAACAAAAATCTAA[A/T]CTATAGTTAAACAAA | 11124 |
rs528000448 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50956033 | AAGTACGGTAACAGA[C/T]TTTCAAGATGAAAAG | 11124 |
rs528000930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863614 | AAATTCAGTATTTTA[C/T]TGAGGATTCTTGAAT | 11124 |
rs528005499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612400 | GTGGAGAAACCTCAT[A/T]ATTTTAGAGAGCTAC | 11124 |
rs528008428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50506214 | ATATATAGAACTTTA[C/T]ATTCTGAACCACTTG | 11124 |
rs528020642 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50906886 | TTATTTCTCCTGCCT[A/G]GTTGCCCTGGCCAGA | 11124 |
rs528020709 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50760930 | GATCAACAAAATTGA[C/T]AGACCGCTAGCAAGA | 11124 |
rs528024510 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50875032 | TTCCCTTCCCAGAAG[C/T]GTGAGAAAGTTATAC | 11124 |
rs528026196 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50554037 | CTGCTAAGGACACGT[A/C]TAATCCCTAACTCTA | 11124 |
rs528027351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608235 | GTGTTCCCATGGTAA[A/T]GGTAAACAGACATGG | 11124 |
rs528036662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454834 | ATGAGTCTGTCTCTC[C/T]AGCCAGGTTGAATTC | 11124 |
rs528037570 | in-del | -/AT | 0.00597962 | 0.0543512 | intron-variant | FAF1 | GRCh38.p7 | 1:50694057 | TGACATGTATGACAT[-/AT]ATATATGACATATAC | 11124 |
rs528038841 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50907046 | TTATTATCTTGAGAT[-/A]ACGTCCCATCAACAC | 11124 |
rs528046528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50442333 | TTAGTGGAAACGACA[A/C]AGGCTTTGGAATTAG | 11124 |
rs528053358 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641455 | TCATGAATTTAAAAA[A/T]ATAGTATGTTTTTTA | 11124 |
rs528063419 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50514808 | GATTGCCATCTCAGT[A/G]TCTGCTTTAGATGAA | 11124 |
rs528082784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50868659 | ATGATCTGTTTTTTG[A/G]CCCATGTGTTGTATT | 11124 |
rs528084745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726502 | GAGATCAAGACCATC[C/T]TGGCTAACACGGTGA | 11124 |
rs528087659 | snp | C/T | | | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471417 | TTTACTGAAGGTCTA[C/T]TCTAGGAAAACCATG | 11124 |
rs528089271 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50683641 | ATATAGTAATTTTTT[A/C/T]AATGTTTTTGGCCGG | 11124 |
rs528091729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50558934 | GGTAATTTTAAATTA[C/T]CTCAAAGAACATTTT | 11124 |
rs528094472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50451030 | AAGTGGCACTGGGGT[A/G]AGGGCTTCCAGGAAA | 11124 |
rs528100899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860366 | ACACATGTGACAAGA[C/T]CTAATATCCAGAATC | 11124 |
rs528112013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751389 | GCCCATGCTGGAGTG[C/T]AGCAGCATGATCTCG | 11124 |
rs528112267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50813512 | GTTGCCCATGTTGGA[A/G]TGTAGTGGCACAATC | 11124 |
rs528113455 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50661221 | ATCTCATTTAAAAAT[A/T]AAGCCTGTCACACTG | 11124 |
rs528119634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50714019 | CTCGTGATCCACCCG[C/T]CTCTGCCTCCCAAAG | 11124 |
rs528136927 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50953029 | GTAGACATAGGAGAC[G/T]CCATTTTGTTCTGTA | 11124 |
rs528147354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757069 | AATATACAGGGATAT[C/T]CCAAATTCTTGTGAT | 11124 |
rs528148909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653269 | ACTATAACATCAATG[C/G]TAAAATCAGTTTTTC | 11124 |
rs528160440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793756 | TTTGTCATAATAATA[C/G]TCTATAGAGATCTTG | 11124 |
rs528164287 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905078 | TGTGTGATGTTCCCC[A/T]CCCTGTGTCCAAGTG | 11124 |
rs528165684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50494565 | ACTCCTTGCCACACC[A/T]AAGTGAGAAGCTGGA | 11124 |
rs528173895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50552042 | GCTCATGCTCATAAT[C/T]CCAGCACTTTGAGTT | 11124 |
rs528176909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50816064 | AAAAAGCCATTCTTC[C/T]TGGTGTGAGATGGAA | 11124 |
rs528184302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50797875 | AACACCGATTTGGAA[A/G]CTCTATGTAGAAATC | 11124 |
rs528188421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50851472 | GTTTTCCCGCTGTGA[A/G]CTGAATCCCTATTTC | 11124 |
rs528195392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50947528 | AAGTCAATGACTAGT[G/T]ATTTAACATGGTGAA | 11124 |
rs528198539 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50759089 | CCTCATGATCTGCCC[A/G/T]CCTCAGCCTCCCAAA | 11124 |
rs528217560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601533 | CTAAAAATACAAAAA[C/T]TAGCTCGGCATGGTG | 11124 |
rs528217572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905376 | TTAAAGCATCATGAT[C/T]CATAATCCTTTGGAT | 11124 |
rs528226436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518102 | AAAAAATATCCCTTG[C/T]GGTATCCCTTGCAGT | 11124 |
rs528243421 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50675015 | CCTGTCTCAGCCTCC[C/G]AAGTAGCAGGGATTA | 11124 |
rs528254645 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50827023 | TGCCTCTGCCCGGCC[A/G]CCCCGTCTGGGAGGT | 11124 |
rs528255816 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50585961 | GGGAGGCTGAGGCAG[A/G]AGGATCACTTGAGCC | 11124 |
rs528260424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50884484 | AGTAAGCTGAGATCA[C/T]GCACTCCAGTCTGGG | 11124 |
rs528275809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736421 | ATGCTATATAACTTA[C/T]TAGGATATTGTTTGT | 11124 |
rs528276343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457674 | AGGCAGACTGCTTGA[C/G]GTCAGGAGTTTGAGA | 11124 |
rs528276484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50727279 | ATTATAAACCAGATA[C/T]ACCTCTATACATATT | 11124 |
rs528277011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50827335 | TAACCTTACCCCCAA[C/T]TCCGTGCCCTCTGAA | 11124 |
rs528279274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50675829 | GATAGTTATAATGAT[A/G]AAGATATCAATAAGG | 11124 |
rs528301253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50575096 | TGTATTTTTAATAGA[C/G]ACGGGGTTTCACCGT | 11124 |
rs528322924 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836962 | GTTTCTTTTTTTTTT[-/TTTTTTTTTTTTTT]GAGATGGAGTCTTGC | 11124 |
rs528323801 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50548845 | CAAAGACTATGGAGT[C/T]GAACAAATCTGATTT | 11124 |
rs528328926 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830591 | ATATTTTGTAATCTG[A/G]ATAGAATTTGTTATT | 11124 |
rs528329112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50630160 | TATTTATTAATAAAG[C/T]AAAGATAATACAGAA | 11124 |
rs528337685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50622441 | TCTCTCCTAAGAGTT[A/G]CCCAAATTATGCTGA | 11124 |
rs528356413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772272 | AATTAGTTCAGCCTT[C/T]GTGGAAAGCAGTTTG | 11124 |
rs528364768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820481 | TTACCTTTTGTGTGC[A/G]TGTGTGTGTGTGTCC | 11124 |
rs528372600 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50581526 | TTTTACTAAGTACAG[A/G]GACATAAAGGATAGT | 11124 |
rs528373807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50511792 | GTCAAATGGTATTTC[C/T]GGTTCTAGATCCTTG | 11124 |
rs528376331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614907 | GAGAATGTGAGCATG[A/G]TTTATTTTTATTTTT | 11124 |
rs528376360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50623331 | CTAGCACTTTGGGAG[A/G]CCAAGGCGGGTGGAC | 11124 |
rs528395081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50867860 | AAAGAAGTCATTATA[C/T]GAAAAAGACTCTTGC | 11124 |
rs528397531 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50713247 | AAAGAAATAATGAAA[C/G]AGTTAAAAAAAAAAA | 11124 |
rs528399273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510903 | TCTATTTTTTAACTC[A/C]GTGTCAAGTACATAG | 11124 |
rs528400744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518592 | ACTACAGGTGCCTCC[A/C]ACCACGTCTGGCTAA | 11124 |
rs528406762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50449820 | ATGCTATGAGTAATC[G/T]ATTCTATTAGTTACT | 11124 |
rs528416095 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50622462 | ATTATGCTGACTTGA[A/T]GATTTGGTCTCTCTC | 11124 |
rs528421500 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961078 | TCTCGCACTGTGGCC[A/C]GGGCTGGAGTGCAGT | 11124 |
rs528430953 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50652135 | TGCAAATGGCAATAA[C/T]GAGGCTAAAAGAATC | 11124 |
rs528438968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50458486 | TATATTCATTGTCAT[C/T]GCTCCCCACCATTCC | 11124 |
rs528440178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933408 | AGGGGCACAATGCCA[C/T]CAGTCTCTTTGCTTA | 11124 |
rs528446615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925308 | AGACAACAAGAATAG[A/G]CAAATGGGACTGTAC | 11124 |
rs528452789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50774770 | ATCTAACAATATACA[A/G]TAATCCCTACCCTCA | 11124 |
rs528472619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50569747 | ACTTTGGGAAAGAGA[A/T]TAGTGATTTACATTG | 11124 |
rs528488186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469123 | TGTTGTAAATATTAT[A/G]TAAACAGTTTTTATC | 11124 |
rs528488834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50830064 | CAGTATGTCTAACTC[C/T]CTCTTCATGACCCCC | 11124 |
rs528492292 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50863560 | CAAAACTACAAAAGA[C/T]AAATGAAACAAAAAG | 11124 |
rs528502042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50568497 | TCAAAGGTAAATTTC[A/G]TAATAGATGAGGGTA | 11124 |
rs528511708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904178 | CATACAAGAGAGTAT[C/T]ATTCAGCCTTTGAAA | 11124 |
rs528520395 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50654966 | TTGCTTGGTTTTAGA[C/T]ATTTCTTTTTTTTTT | 11124 |
rs528524609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872535 | TGACATAACCTTAAC[C/T]GATAAAGCAGCAGTA | 11124 |
rs528524855 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50624454 | GCCCGGCCAACTTTC[A/C]AACTTTCTAGTGTTC | 11124 |
rs528537241 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619758 | TATCTAACCAGGGTT[C/T]TCTGTATTTCCTGGA | 11124 |
rs528537385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50926109 | GTAATCCCAGTTACT[C/T]GGGAGACTGAGGGGG | 11124 |
rs528575350 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469751 | CTTGGGCAGTGGTAT[A/G]GAGGGAAAGAGAAGA | 11124 |
rs528575870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50775546 | TGTGTAGGAGTTTTC[C/T]GGAAAGCTAAAGCAA | 11124 |
rs528596996 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50877868 | AGCTCTCAGAGCACA[C/T]AGTACTTGCTGCAAG | 11124 |
rs528600374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50520220 | TGTTTCCTGGGATGA[C/T]AGGTAATTGGAAAGA | 11124 |
rs528607683 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50614825 | GCCTGGGCCGCAACA[-/G]CGAAACTCCGTCTCA | 11124 |
rs528607967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50513344 | CAAAAATTAACCGGG[C/T]ATGGTGGTGCATGCC | 11124 |
rs528618233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689746 | CACAATGGAATATCA[C/T]TCAGTCTTAATGAAT | 11124 |
rs528629170 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50942747 | TTTTAGTTGTCGTTG[-/T]TTTTTTTTTTTTTTA | 11124 |
rs528631279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452295 | GACACAGGCAAATTC[A/G]TAAGTGAAGATTCTG | 11124 |
rs528636186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662045 | AGCTTTTTTTTTCTT[C/G]CCCCTTCCCCCAGGG | 11124 |
rs528647034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948278 | ATTCTTGTGTTGCTA[G/T]AAAAAAAATCTGAGG | 11124 |
rs528652325 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50842966 | ATCCCCTGTGCCTAA[A/T]ACAGTGCTAGCACAC | 11124 |
rs528662611 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | FAF1 | GRCh38.p7 | 1:50585881 | ATCTCATCTCTACAT[A/T]AAAAAAAAAAAAAAA | 11124 |
rs528672014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50745055 | CACTTTGAGAGGCCA[A/C]GGTGGGCAGATCACC | 11124 |
rs528681956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534872 | AATATGTTTAGGAGG[A/T]TGAGAAAACACCTGA | 11124 |
rs528690894 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50720241 | TCCTGACAGGTGATC[C/T]GCGTGCCTTGGCCTC | 11124 |
rs528693342 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50745727 | TGAGACAATTAAACT[C/T]TTTTTCTTTACAAAT | 11124 |
rs528693969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50646893 | CTCTGTTACCCAGGC[C/T]GGAGTACAGTGGCAT | 11124 |
rs528704174 | snp | C/T | | | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50962061 | TCACATGAATCAAAA[C/T]GTCTTGCTTAATTTT | 11124 |
rs528704830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845872 | TCATGCCTGTAATCC[C/T]TGCACTTTGGGAGGT | 11124 |
rs528708350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890078 | TGTATATTTAGGATA[C/G]TTAGCTCTTCTTGTT | 11124 |
rs528719818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486936 | GCATTTCTCTAGTTA[C/G]TATAAAGTCCATCCC | 11124 |
rs528722595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639635 | CTTCCCTCTTCTTTC[C/T]TTTTTAAGTAACAGC | 11124 |
rs528733843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728870 | AAGCTGTAGTTTTAT[A/G]GAGAGGACTAGTTCA | 11124 |
rs528738119 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50679780 | CAGGTAGTTGCATGT[C/T]ACAGACATTCTAAAT | 11124 |
rs528740016 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50837402 | TGCCACTAACAATTT[G/T]AAACTATTTTATAGA | 11124 |
rs528745510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50631531 | AGAGTAGTGATGTTG[C/G]CAATTCAGATATGAC | 11124 |
rs528746922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890524 | TTTTCCATGTTTAAT[A/G]CTTCCTTCAGGAGCT | 11124 |
rs528749408 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783229 | ATCAGTAATCAAAAA[C/T]CTCCCAACAAAGAAA | 11124 |
rs528759486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50640418 | CTGCCCCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 11124 |
rs528762761 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50605626 | AATAGCCCTTCTTTC[A/G]CAGTTCCTATCACTA | 11124 |
rs528768023 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50539207 | ATCTTCAATATACAG[C/T]GACTGGATTTTCTAG | 11124 |
rs528782145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50623915 | TGCACTCCAGCTTGG[A/G]TGACAGAGCGAGACC | 11124 |
rs528783459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632313 | TCTAAATAAGACTGA[A/C]AGGTTAGAAACGAGT | 11124 |
rs528796675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932723 | GACCTAGCAGGGACT[C/G]TGTGTGGAGGCTCTG | 11124 |
rs528822796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50527010 | CATGTGCGTGCCACC[A/G]TGCCCAGCAAAGATT | 11124 |
rs528827158 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50589071 | TTGCAAGCACAGTGG[G/T]AGGGGCAGGAGCCAA | 11124 |
rs528836148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50464512 | GGGGAATGCAATAAA[C/G]AGTGGACTTTCTTCC | 11124 |
rs528840719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515882 | TCCAAGCTGTATCAC[A/G]TACCCAAATTTTTAT | 11124 |
rs528841021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50782481 | GATATAAAGAAAAAA[A/G]CATTTGTACAACTGT | 11124 |
rs528844082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50733779 | TAAGCTACCCAGTCT[A/G]TGGTACTTTGTTATA | 11124 |
rs528845170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523212 | GCTATTATGAATAAT[A/G]ATGCAATGAACTTTC | 11124 |
rs528848863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778195 | TGATTTCAATTATAC[A/G]AAGGTCAAAATACAC | 11124 |
rs528853555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937218 | TGTGCACAACTAGGT[C/G]AAAGTCCACTCTACT | 11124 |
rs528856004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581914 | TGCTGATGTCTTGAC[C/T]GCTGTGACAACATAC | 11124 |
rs528858572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50907096 | TAGCATGAAGGGCTA[C/T]AGAATTTTGTTGAAG | 11124 |
rs528860994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50455055 | TCTTCCCCCAGCCTC[A/G]TTCCTACAGCAGGCA | 11124 |
rs528863507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50680448 | AGAACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 11124 |
rs528867006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888622 | GGCCTTTTCTGCATC[A/G]ATTAGGTTTTTGTCT | 11124 |
rs528871402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50573494 | GGCCCAGCAATGTCA[A/G]TGGCCCCATATGTTC | 11124 |
rs528876646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463835 | GAAGGCTCAGGCCCA[A/G]CTGTTCTTAAAACTA | 11124 |
rs528882901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834078 | CGGATTTCCCCCTTG[C/G]TGTTCTCATGATAGT | 11124 |
rs528895548 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50696170 | CTCTCTCATTCCATA[A/G]TGTAATCCTGGATTT | 11124 |
rs528901470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725713 | CACCCTCCTCCGCCT[C/T]CTAAAGTGCTGGGAT | 11124 |
rs528904277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50673087 | ACATGGTGAAACACC[A/G]TATCTACTAAAAATA | 11124 |
rs528904399 | in-del | -/GTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50728269 | GAAGAAATGAGCCAA[-/GTT]GTTGTTACCTGGTAG | 11124 |
rs528908070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50572982 | GGGATTACACACCTG[A/G]CCTGCGAAGGTGATA | 11124 |
rs528919610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50764327 | AGTATTCTAGTCTTA[C/T]GTATAAGGTCGAGGA | 11124 |
rs528925354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50627620 | CAAATAGTACATACC[A/G]CATGATTCATAATAT | 11124 |
rs528940924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928901 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 11124 |
rs528949448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50564230 | CTATAATATCAGATG[A/G]TAGTCCTAGGAAACC | 11124 |
rs528958642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874015 | AAGCAACTGTAGAAA[C/T]GATGCAGGGTATGTG | 11124 |
rs528969030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50826195 | GAGTAAACAAATACT[A/C]TTTCTTGTGTGGAGA | 11124 |
rs528972241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50613241 | CTATCTGATTGACAT[C/G]TGGGCCTCAGTGAAA | 11124 |
rs528972282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621519 | GTTCTCCTGCCTCAG[A/C]CTCCCAAATACCTGG | 11124 |
rs528977104 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50922172 | ACTCCGTCTCAAAAA[A/C]AAAAGGCCAGGCGCA | 11124 |
rs528978817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778880 | AGAGCTTGCTGCATC[A/G]ATTAACTTCCTTTCA | 11124 |
rs528989733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50519286 | GTGAGTCGAGACCAC[A/G]CCACTGCACTCCAGC | 11124 |
rs528996315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50761594 | GACAAAAACCACATG[A/T]TTATCTCAGTAGATG | 11124 |
rs529013578 | snp | A/G | | | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475482 | TCTCCTAGGAAAGGT[A/G]CTCAGTAACTTGTAC | 11124 |
rs529016747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50596420 | CTAAGGCTAATTTTC[A/T]TTAGATGATAGACTG | 11124 |
rs529021318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50455769 | CCAGGAGACATGGTT[C/T]CCAGCTTAACCCCCT | 11124 |
rs529022369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50818901 | ACAAATTCATTTATG[C/T]TTCATATATATCTTA | 11124 |
rs529034507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50665404 | GGATATTCATTGCAG[C/G]CTTGTTTATCATCAC | 11124 |
rs529035496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50856070 | CACTACCAGTAAGTG[C/T]TTTAACCTTCAAAAT | 11124 |
rs529036005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951002 | TTGGGAGGCCGAGGC[A/G]GGCAGACCACTTGAG | 11124 |
rs529041891 | snp | C/T | 6.12364e-05 | 0.00553303 | intron-variant | FAF1 | GRCh38.p7 | 1:50539774 | TGCTTTGTAGTTTAA[C/T]AGATTTACTAGTACT | 11124 |
rs529042673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50692911 | CCAATTTTCAATTAG[A/G]TTATTTGTCTTTTTA | 11124 |
rs529063098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943549 | GCCTTCCAGGGCCAA[C/G]GTGTTGTCATTGGTT | 11124 |
rs529069577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50481961 | GGTGATTAGATCATA[C/T]ATGGCTTTGGGAAGG | 11124 |
rs529074849 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | FAF1 | GRCh38.p7 | 1:50479203 | ACATCTTCCTCACAG[A/C]ATCCTTCTATAAGAT | 11124 |
rs529086749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50539182 | AACAATTGTCACTGT[C/G]AAAAATTCAATCTTC | 11124 |
rs529087844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748736 | TAGGTTGCTGCTAGT[C/T]TACAGTTTCAGATTA | 11124 |
rs529090474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50840418 | TAATAAGAAGAAAAT[C/T]CAAATATAATGCACA | 11124 |
rs529097748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50740931 | ATTTGATCATTATTG[C/T]TCTTTTTCCATGCCA | 11124 |
rs529101240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892911 | CTGTCTCCTCTGACT[G/T]TATTTTTAAGCAGGT | 11124 |
rs529101490 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50670874 | GGTGAAAGATGCAGT[A/C/G]AGCTGAGATCCCACC | 11124 |
rs529102290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50791458 | AGAGGAGACACTATC[G/T]AGAGATTAGTAGTTA | 11124 |
rs529102855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50490469 | AGGAAGGAAAAAGAA[A/G]GAAGGAAGGAAGGAA | 11124 |
rs529106046 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50828565 | TGAGCCACCGCGCCC[A/G]GCCAAGAAGGGTCTT | 11124 |
rs529113905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50480636 | ACACACATAAGAAAA[C/G]ATAGTATGTGCCACA | 11124 |
rs529123691 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50901710 | TGTCTACAAAAAATA[A/C]AAAAATGTGTCGGGC | 11124 |
rs529134569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50642943 | CCTCCCAGGTTCAAG[C/T]GATTTTCCTGCCTCA | 11124 |
rs529143892 | in-del | -/A | 0.366266 | 0.221319 | intron-variant | FAF1 | GRCh38.p7 | 1:50622164 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAATA | 11124 |
rs529147332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50741917 | CAGTTTGGATATGTG[A/G]ATTCAAAAAAGTATG | 11124 |
rs529149635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50589361 | CTGCTGAGGAGGGAT[A/T]CTAGACCCAAGCAGG | 11124 |
rs529154149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50635606 | AATTTTTGTATTTTT[A/G]ATAGAGATGGAGTTT | 11124 |
rs529161446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893590 | GCTGGGGGTGGGGTG[A/G]CACAAGTACTCCTAT | 11124 |
rs529163102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50794550 | AAAATTGGAAAACTG[A/G]GTGACAAGAAAGTCT | 11124 |
rs529166731 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50589874 | ATATTAGGTAAGGGT[A/C]CAACTTCATTCTTTC | 11124 |
rs529169312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50693869 | GATTTCTAAATTCCC[A/G]CATAATGACCAAATT | 11124 |
rs529173933 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50643656 | AGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACAGC | 11124 |
rs529178986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636374 | CTCTTAGTTTGGGGC[A/G]TGTCCTTTTTTTTTT | 11124 |
rs529182038 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50686344 | GGCCAGGAGATCGAG[A/G]CCAGCCTGACCAACA | 11124 |
rs529182570 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50549467 | GCATGCACCACCATG[C/G]CCAGCTAAGTTTTAA | 11124 |
rs529187433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50590211 | TGCAAAAAACCACCA[C/T]TGGAATTTTGATACG | 11124 |
rs529194510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786031 | CCTGCTACTCAGGAG[A/G]CCAAGGCAGGGGGAC | 11124 |
rs529196034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50936527 | ATTACAAGCATCAAA[A/G]TATTACTACAGCAGA | 11124 |
rs529197798 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50564907 | GTATTTTCCCATTTG[C/G]CTTAACAGTAGTAAT | 11124 |
rs529206975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50686922 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT | 11124 |
rs529208554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786602 | AAAATTTTTTTAAAT[A/T]AAAAACAATCTACAG | 11124 |
rs529217605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50533454 | TGTTCATTTATTCAA[C/T]TGCTTAACAAACATT | 11124 |
rs529228865 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849846 | ATGGCTTTATTAAAG[A/C/G]TATCATATAATGCAT | 11124 |
rs529231548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50531057 | ACGTTATCTTCCCTA[C/T]AGTGTGGCAATGCTG | 11124 |
rs529235078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888209 | TATGAATGCTTGTGA[C/T]TTTTGCACATTGATT | 11124 |
rs529239370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50679755 | TATTGGTAACTGCTA[C/T]TTATTTCCACAGGTA | 11124 |
rs529242948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50687808 | TGCAAGCCAGAACCA[C/T]GATCAGATACCACTT | 11124 |
rs529248122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644724 | AATATCTGAAAACAG[C/T]TGTTTCATGTATTTT | 11124 |
rs529249482 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50581373 | CTAGAAAATAGAAAT[A/C]TCAGAGGCATCCTTG | 11124 |
rs529277081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50541336 | CCAGACCTCATGGCA[A/G]TTTCATATCAGTGCC | 11124 |
rs529278928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50485482 | CCTGGCTAACACGGT[A/G]AAACCCCGTCTCTAC | 11124 |
rs529283388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645421 | TTGGCAAACTTTCTC[C/T]GTAAAGGGCCAGACA | 11124 |
rs529303824 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707037 | TAAAACCCCGTCTCT[A/G]CTAAAAATGCAAAAC | 11124 |
rs529310008 | snp | A/G | 5.35834e-05 | 0.00517579 | intron-variant | FAF1 | GRCh38.p7 | 1:50452181 | GTTTCCCCATCCTGG[A/G]AAGTCCTGGAATCTG | 11124 |
rs529326994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50627033 | GAAGATCAGGCATGC[A/G]CAGGGAATAATATGA | 11124 |
rs529335668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938123 | CAATGCCAACCATAC[C/T]ACTAAGAATATTCTG | 11124 |
rs529336443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638054 | CTTAAATATTTCATG[G/T]TTTTGGATAGAATTG | 11124 |
rs529336981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525165 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 11124 |
rs529337322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50788392 | CTGAAGGCCACATTA[C/T]TCTCCTTCCCATCCT | 11124 |
rs529342041 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50474677 | TCTACTAAAGGAATC[C/T]ATTTCTACACATTTC | 11124 |
rs529344281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50843263 | TTCTTTTTCTTCATT[G/T]TATGGATATATAATA | 11124 |
rs529349984 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50889203 | TTTCTGTGGGATCGG[C/T]GGTGATATCCCTTTT | 11124 |
rs529351344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50789365 | TACTTAGTAAGATCC[C/T]GGACCCCCAACTCAG | 11124 |
rs529351443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779746 | AATAGATTCATATAA[C/T]TATAAGATGTCTTAT | 11124 |
rs529361359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904304 | TTATATGAGGTACTA[C/G]AGTAGTCAAATTCAT | 11124 |
rs529363387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688331 | TGATTCAGCAATCCC[A/C]TTTCTTGGGTGTATA | 11124 |
rs529383101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50835169 | ATTTTCATTCTATCA[A/G]TGAAGAGAAGCACTA | 11124 |
rs529395721 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869104 | TACCTTCTTGAAAAA[C/T]TGATTCTCCCGCGAT | 11124 |
rs529401866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682006 | GCCTGGCTAATTTTT[A/G]TATTTTTTTGTAGAG | 11124 |
rs529405114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50930134 | CATTTCAAGAGAGGG[A/G]TATCTTTGAAATGTA | 11124 |
rs529405562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591556 | TGGGTGCCTATAATC[C/T]CAGTTACTCAGGAGA | 11124 |
rs529417291 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50889556 | TCCCAGAGGTTCTGG[C/T]ATGTTGTGTCTTTGT | 11124 |
rs529429111 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50859742 | TTTGTCACAAACTAG[-/A]AAAAAACTAAAATTC | 11124 |
rs529438870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50883816 | TTAATTTACTGAGAC[A/G]TACAGTATTGAGTAT | 11124 |
rs529439614 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50501101 | AAAGAAAGTCATAGT[A/G]ACAAAACCATAGACT | 11124 |
rs529440994 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50606346 | AATGATGCCGACCAA[C/T]GTTAAAGAAAAATTT | 11124 |
rs529441083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50783238 | CAAAAATCTCCCAAC[A/G]AAGAAACATGCAGAT | 11124 |
rs529452542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50666150 | AAAAAAAAAGACCAG[G/T]TGATCTGCCCGCCTT | 11124 |
rs529468505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50915255 | CATGCCTGTAATCCC[A/G]GCTACTTGGGAGGCT | 11124 |
rs529470848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50547987 | GACTCTTAGGAGGGA[C/T]AATAGAGAACATCTA | 11124 |
rs529471348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50687719 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 11124 |
rs529471646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866868 | GAAACCGAAAAAGTG[A/G]CCATATAGCCAAAAT | 11124 |
rs529473412 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50652471 | AAGCCAATTTCAGTC[A/T]GGTTTCTACAAGGGT | 11124 |
rs529477277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657763 | CACTACGGAAAGGAG[A/G]AACAAAAAATAAAAC | 11124 |
rs529484325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447711 | CATCTCATCTTACCT[C/T]TTACGCCAATGTCAA | 11124 |
rs529490037 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50958704 | AAAATTAATTAATTT[A/T]AAAAAAAATAAGGAA | 11124 |
rs529491119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50499027 | GTATATACCTACAGT[A/G]GAATATTATTTAGCT | 11124 |
rs529494270 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50901743 | GGTGGTGCATGCTTG[A/C]GGTCCCAGCTACTAG | 11124 |
rs529494819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50711594 | CCTGCCTCGGCCTCC[C/T]GAGTAGCTGCTACAG | 11124 |
rs529504511 | snp | A/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467908 | CTACAATGAATACAT[A/G]TATCAAAATATCACA | 11124 |
rs529517331 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50491848 | ATATAACTTTTTTTT[G/T]AAAAAAAAGAGAAAA | 11124 |
rs529517445 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50448939 | ACGAGGGTCACAGCT[-/T]TTTTTTTTTTTTTTT | 11124 |
rs529518165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50959202 | AATATATAGTCTTAT[C/G]TGTCTCCTTGTTATC | 11124 |
rs529525022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50555859 | ATAGGGAATCAACTT[C/T]AAGTACCCATTAACC | 11124 |
rs529525469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565170 | TTTAAATTTGTAATA[C/T]GGACAGAACTATTAA | 11124 |
rs529535913 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50753992 | CGATCTCCTGATCTC[A/G]TGATACGCCCACCTT | 11124 |
rs529537763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50556131 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 11124 |
rs529540379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50509583 | TACCACTGCATTCTA[A/G]CTTGGGCAATGGAGT | 11124 |
rs529552957 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50491032 | TCTATCCATCCTCCA[C/T]GCATTCTGGACCCTT | 11124 |
rs529558238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908710 | CCCTGCCTTTTTTTT[C/T]GCTTTCCATTTGCCT | 11124 |
rs529559504 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50807719 | AGTCAGACAAAAATT[A/T]AAAAAAGAGATTCAA | 11124 |
rs529565856 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50841136 | CAGCAATGGCTCCAC[C/T]ACAGCAGTAAGAAAA | 11124 |
rs529573016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50951951 | GAAAATATTATAAAC[G/T]GACAGAAACTACTTA | 11124 |
rs529586241 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50598488 | AAAAAAAAAAAAAGG[C/T]TAAGTTTTCTGTTCT | 11124 |
rs529598086 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50814536 | AAACATTATAGATAT[C/T]CAAAAAACAAGCCAA | 11124 |
rs529598172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50548719 | ATATAATTTCATCCT[A/G]TCACCACCCACTGAC | 11124 |
rs529605455 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50538673 | ACACTAGTTCTTGCA[A/C]CATTGCCTCTGACAG | 11124 |
rs529605619 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50579601 | ATTCAGCATTATTTT[A/T]CAAAGCATGTCACCT | 11124 |
rs529609568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849181 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAA | 11124 |
rs529610713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50866174 | ATTAAAACCCTCAGC[A/T]AAATCAGCATAGAAA | 11124 |
rs529618075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50690620 | AAACAAACAAACAAA[A/C]AAAACTGTTGCATAC | 11124 |
rs529618813 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705183 | GTGGCTGGGGCCCAA[C/G/T]GCATACCAACAAGGT | 11124 |
rs529622025 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50545584 | CTAAAGCTATATTTT[A/T]AAAAAAAAGAAAAAA | 11124 |
rs529624464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50749619 | AGCAAGACACCACCA[C/T]TGCAAAAAATTTTTA | 11124 |
rs529633689 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50952318 | TTTCGCCGTGTTGGC[C/T]GGGCTGGTTTCCAGC | 11124 |
rs529634818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50655164 | AGTAGTGGGATTAGA[A/G]GCGGCCGCCACCATG | 11124 |
rs529640138 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50948772 | CTCAAGTGATCCACC[A/G]GCCTTGGCCTCCCAA | 11124 |
rs529652973 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50599806 | GGCAGACAAACTGTG[C/G]TTATTTGGATTTGGT | 11124 |
rs529665126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50898211 | CCCAGGAGGCTGATG[A/G]GAGGATCACTTGAGC | 11124 |
rs529668304 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50853068 | CTCAATGCTTGGCTG[C/T]TTTCGGATGAGGACA | 11124 |
rs529673591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648184 | AATTGCTCGAACCCC[A/G]GAGACAGAGGTTGCA | 11124 |
rs529674261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50594116 | TCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACATA | 11124 |
rs529687122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50640766 | CTTATTAATTACTGG[C/T]ACTGTTAATTCATAT | 11124 |
rs529699588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941745 | TGTGGGCATAACAAT[A/T]GAAGGGAAATATGTT | 11124 |
rs529718757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50799590 | CAAAGGAATTTAGTA[A/T]CAACACATGTATCAG | 11124 |
rs529746005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50783562 | GAGATTTATCCCTGG[A/G]ATGAAAGGATTATTT | 11124 |
rs529756049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846446 | CAGCTCGCTTCCGAG[C/T]CGCACGCATCGAGCC | 11124 |
rs529757244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933625 | TTCAACCTCTGCCTG[C/T]TACCCAGTTCCAACG | 11124 |
rs529763869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50641442 | TTTCTTCTTTGACTC[A/T]TGAATTTAAAAAAAT | 11124 |
rs529765243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50527952 | CACAGCTCACTGCAG[C/T]CTTGACCTCTTGAGC | 11124 |
rs529765305 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50543511 | TTAAAACACTTGTCT[G/T]CTTGTAAGGATGAAA | 11124 |
rs529772241 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50639466 | TTTTCCAGGACCTTA[A/T]TCACCTGATTGTATA | 11124 |
rs529784213 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50494417 | TCCCTTTGCTAAATC[A/T]AAGAGGACACATCAA | 11124 |
rs529791426 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50617439 | AATTCTGTTTATGTG[A/G]TGAATCACATTTATT | 11124 |
rs529791886 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50766164 | CAGACCTGTTACCCA[A/G]AAGCAACAAAACATG | 11124 |
rs529792675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691262 | CACCTTTTTTTTTTT[C/T]CAGACAGTTTCACTC | 11124 |
rs529797769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886788 | TATCATTGATGGACA[A/T]TTAGGTTGGTTCCAA | 11124 |
rs529800807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50633323 | AGTTTTATTCGTAAA[A/G]TCAGTCCTGTATCTT | 11124 |
rs529801804 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50648978 | TTAGTAGAGACAGGT[G/T]TCAATACGTTGGCCA | 11124 |
rs529802870 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | FAF1 | GRCh38.p7 | 1:50942469 | GAGGGGAGGGAAAGG[A/C/G]AGGGGAAAGGGAAGG | 11124 |
rs529811488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50594740 | GCTGAGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 11124 |
rs529814181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452261 | TTTGCAAGCTCATTG[C/T]CCCTGAAAGCATAAA | 11124 |
rs529826673 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50955021 | AAAAGAAAGAGGTTA[-/AGG]AGGAGAAGACTCTAG | 11124 |
rs529832095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50661311 | AGAACGCTACTGTGA[C/T]ATAGTTTTCAAGTTT | 11124 |
rs529837332 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | FAF1 | GRCh38.p7 | 1:50882918 | TTGAACACGGGAGGC[A/C/G]GGTTGTAGTAAGCCG | 11124 |
rs529845531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50891819 | GAGGGACACACTTGA[A/G]GAGGCAGTCTGTCCG | 11124 |
rs529853481 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783338 | ACTGAAGGAGGGAAT[A/G]CTTCCTAACTTCTTT | 11124 |
rs529856339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910427 | CTGTCAGACAGGGAA[A/G]TTTAAGTCTGCAGAA | 11124 |
rs529863564 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50821247 | ATATGCCAGTGGAGC[A/G]TAAATATCTGCCTCA | 11124 |
rs529863954 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50857248 | TCTAAACTCACTTCT[A/G]TAAGTACACATCTTA | 11124 |
rs529875894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50443533 | ACAGCCATATGGTTA[A/G]TAAGTGTCTATAAAG | 11124 |
rs529881397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50670209 | CAGCCGGGGGTGAGA[C/T]AGGGGAGGGACAGAG | 11124 |
rs529884859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50617529 | AATTAAGTTTTTGAG[A/G]TGCTTCCGGATTCAG | 11124 |
rs529886446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513297 | CCAGCCTGGACAAGA[C/T]GGAGAAACCCTGTCT | 11124 |
rs529894861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609100 | ACTGAACAACCACAA[C/T]GTGTCAAGACCTCAG | 11124 |
rs529895102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50654376 | TTTACTTTTACTTTT[A/T]AAAAAAACTTAGGTA | 11124 |
rs529928309 | snp | A/T | 0.00363344 | 0.0424679 | intron-variant | FAF1 | GRCh38.p7 | 1:50714995 | TAACAGATATAAAGT[A/T]AAAAAAAACCTGTTG | 11124 |
rs529936337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50905599 | TGAGATGGTATCTGA[C/T]TGTGGTTTTAATTTG | 11124 |
rs529949262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50494844 | AGTGCTCAACAGTTA[C/T]ATACTAGAAATTCAG | 11124 |
rs529963619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495434 | ATGTTGTTGCAAATC[A/G]CAGGATCTAATTCTT | 11124 |
rs529967398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815350 | GAGTTAATTCGCTTA[C/G]GATTATGGCCTCCAG | 11124 |
rs529973302 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50905919 | TGGCTTTGGTTGCCA[C/T]TGCTTTTGGTGTTTT | 11124 |
rs529986873 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50609797 | GTTGAATTATGGAAA[A/C]AAAAAAAAAGTTAAG | 11124 |
rs530003387 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50446356 | TAATGTAAAAATCCC[A/C]AATATTTCAAAATCC | 11124 |
rs530008092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50920403 | GTACAGCCCCAAGTA[C/T]TACTGCAGATGACAG | 11124 |
rs530008466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707852 | TCTCACACAGAAATG[A/T]TGCCTTCTGGAAACT | 11124 |
rs530012190 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50816218 | TTCTTTTTTTTTTTT[G/T]TTTTGAGACGGAGTC | 11124 |
rs530015169 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50646618 | AATGTCCCTTTCACT[A/G]AGAAGTCATTTTTTC | 11124 |
rs530017544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862301 | AAAGTCTATCAATCA[C/T]CATCTTAAACATACT | 11124 |
rs530019074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708357 | ATGGAGTGTGAGAGA[A/G]AAACATAACCCCAAG | 11124 |
rs530031133 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681051 | TAATAATAATAATAC[A/G]ATGATGATGATTTGA | 11124 |
rs530037639 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50698737 | TATCCCTCCTCACCC[A/T]ATAACTTACATTTCA | 11124 |
rs530037950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50954785 | TGACCTCAAGTGATC[C/T]GCCTGCCTCGGCCTC | 11124 |
rs530040733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50920247 | CAGAGGGTTGCAGTG[A/G]GCCAAGATCGCGCCA | 11124 |
rs530043502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453820 | AGCCTTTTCTTCATG[C/T]GTATTCCCTATCAGT | 11124 |
rs530045113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551790 | CATCAGGAAATTCAA[A/T]CTGTAGAATGCTACC | 11124 |
rs530052750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562286 | ATGCTGGATGAATCA[C/T]TAACAAAACATCTTC | 11124 |
rs530054695 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50480428 | ATGTATAAATAACGG[C/T]TTATAGCTGGCTGAG | 11124 |
rs530059685 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50664301 | GTGCCCGGCCAATCT[C/T]TAGTTTTTCTGTCTC | 11124 |
rs530064334 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50444312 | AAAAGCTATGTTCTC[C/T]GAGAGACAGCTAAAG | 11124 |
rs530068619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760428 | CCAAAATTGACCACA[C/T]AGATGGAAGTAAAGC | 11124 |
rs530069307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50717265 | ATGATTATTTGGATA[C/T]GGGGTCTTTGGGAGG | 11124 |
rs530073192 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50817011 | GTGCAGCATTATTTC[C/G/T]GGGTTCTTCACTCTG | 11124 |
rs530088148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50663699 | TGAGCCACCGCGCCC[A/G]GCCAGAAGCACCGCT | 11124 |
rs530092995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956495 | TTCCTACAAAGATAA[G/T]ACTGAGCTCTCAAAC | 11124 |
rs530095088 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50734439 | TTGGACATTTGAAAC[A/G]AAAAACACATGTAGG | 11124 |
rs530096048 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50563557 | CAATATTTTCCAAGG[-/A]AAAAAACCTCCAATT | 11124 |
rs530108259 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787663 | ATCAAGATATATCCT[A/G]TGAAAAATGAGTAAG | 11124 |
rs530109887 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50777885 | GGTTCGACCATTTTA[C/T]AAAAATGTTTTGCTA | 11124 |
rs530110095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871971 | TCGGGAGGCTGAGGC[A/T]GGAGAATGGCATGAA | 11124 |
rs530114087 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50912580 | CTTTTTAACATCATT[A/C]CTCTGGTTATCACAA | 11124 |
rs530127315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50701229 | TCATTCTAATTGATC[C/T]AATATATGCCATTTA | 11124 |
rs530128014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50656225 | TAATCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 11124 |
rs530128150 | in-del | -/A | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50578899 | TTATAGAAATGTAAT[-/A]AACTGTACATAAACT | 11124 |
rs530132774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760802 | CAAAAGCAAACACAT[A/T]CAAAAGCCAGCAGAA | 11124 |
rs530136575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833388 | GGAAAAGATACACAG[A/G]GTGGTAAGGTGTGTG | 11124 |
rs530138472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863555 | ACAAACAAAACTACA[A/G]AAGATAAATGAAACA | 11124 |
rs530139389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50702101 | ATTTTGCCTAACAGA[A/G]GCTTCTGCAGTAGTA | 11124 |
rs530144939 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50783775 | AGCTACTGAGGGGGC[C/T]GAGGCATGAGAATCA | 11124 |
rs530153806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50957500 | GGGACTACAGGCGCC[C/T]GCCACCTCGACCGGC | 11124 |
rs530154968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50611768 | AATTTGATTCACAAA[C/T]ACCCACCGTACATTA | 11124 |
rs530160234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50604680 | GCCCAGCTAATTCTT[A/T]AATTTTTTGTAGAAA | 11124 |
rs530173873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50490194 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 11124 |
rs530176540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649132 | GAGGGCTGTGTGCAG[G/T]TTTCATTTTATGTAT | 11124 |
rs530177177 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50554765 | TACTGAAAACAACTG[A/T]ATCCAAGTCAGAATA | 11124 |
rs530182717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50497837 | ACAGGTGTGTGCCAC[C/T]GCGCCCGGGCTCAAA | 11124 |
rs530183829 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50744065 | AACAGAGCGAGACTG[C/T]CTCAAAAAAAAAAAG | 11124 |
rs530184241 | in-del | -/A | 0.389734 | 0.207303 | intron-variant | FAF1 | GRCh38.p7 | 1:50751153 | CCCATTTCATGTTAA[-/A]AAAAAAAAAGAGCTA | 11124 |
rs530196517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50603720 | GCTTATCAAGAATGC[G/T]AGTTACCAAGTGTAC | 11124 |
rs530200700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50784428 | AAAAGAAAATTAAGA[A/C]AACAGTCCCATTTAC | 11124 |
rs530202710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50678509 | ACATTTTTTGGTCAG[A/G]TGTGGTGGCTCACAT | 11124 |
rs530204296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685388 | AAGAGTCCGTGTAGC[A/G]AGATAGAAGGAGGGT | 11124 |
rs530218792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50710091 | AGGGCTTCAAATGCT[A/G]GGCTGAGGAGCTCGG | 11124 |
rs530220494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497458 | TACCATAAAGGAATG[A/G]CTTTGTGTCTAGACA | 11124 |
rs530221841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50579753 | TCTTCACAAAGCAAA[C/T]GCCAGGAGGAAAAAA | 11124 |
rs530226549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50801747 | TGGTGGAGAACACTT[C/T]AAAAGGAAATAAGTA | 11124 |
rs530230177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50854989 | AAAGGAAATGCTCGA[C/T]GGAACATTTTGGATG | 11124 |
rs530237800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50671164 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCAGGC | 11124 |
rs530246086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688705 | TAATCCCAGTTACTC[A/G]GGAGGCTGAGGCAGG | 11124 |
rs530251399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50546513 | TGGGATTACAGGCAC[A/G]CGCCACCACACCTGG | 11124 |
rs530263740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521033 | CATACTGTTTTTTAT[A/C]TATTAATTCATTATT | 11124 |
rs530269918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50934185 | TGAGTTAATATTACC[A/G]CACCCCATATAATGT | 11124 |
rs530276999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723325 | AGAATTGCTTGAACC[A/G]GGAGGCAGAGGTTGC | 11124 |
rs530278173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50838949 | ACCAAATTATAAACC[C/T]CTAAGATCAATGTTT | 11124 |
rs530280589 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50566258 | TAACAAAAAGACAAA[C/T]CAGATGGTTTCTAAT | 11124 |
rs530281417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50561681 | AAATACAAAAATTAG[C/T]CAGGCGTGGTGGCAC | 11124 |
rs530284949 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50571765 | AGCTACAGTAGCTAT[G/T]GTATTTAGACTCTTA | 11124 |
rs530289810 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847880 | ACACACAAACAAATG[C/T]ACACATATACACACA | 11124 |
rs530289876 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50806882 | AAAAACAAACAAACA[A/T]ACACATTCAAAGGAT | 11124 |
rs530301176 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50730678 | ACAGAGTTTCCAGTT[C/G]TATACTATACCCAAA | 11124 |
rs530303312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739748 | TAACTTGGATGAGGT[A/C]TCTGGTGTTACCTAT | 11124 |
rs530304396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515288 | AAACTGAGACTTGAA[C/T]TGGCTATGTAACTTG | 11124 |
rs530304983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570935 | CTAATCAGAAAACTG[C/T]TTTCGTGAAGAAAGC | 11124 |
rs530308597 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50606106 | AAAAAAATAAAAATC[A/C]CACACCACCTCATCT | 11124 |
rs530310861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919771 | AGCCACCGCACCCAG[C/T]CGAAGAATATTCTTA | 11124 |
rs530312227 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50927488 | TTGGGAGGCTGAGGT[G/T]GCAGTGAGCCAAGAT | 11124 |
rs530316372 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50823852 | GATCCCAATATAAAT[A/C]GTCCCATTAATGATC | 11124 |
rs530335732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470367 | TCTGCTTTTATAATT[G/T]TTCAAGTGACTTAAG | 11124 |
rs530340752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50521529 | GGTTTCAATTTTTAT[C/T]TGGAAAATACTAAGA | 11124 |
rs530344991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50578846 | CCTGTTTAGATTTAA[C/T]TTTGAATAATTTATC | 11124 |
rs530364432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50731792 | AAGTATCTGATGTTT[A/G]CTATTATGACTTCAT | 11124 |
rs530373382 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50809673 | CACAGTCATTCACAG[A/C]CAAATTCTACCAGAT | 11124 |
rs530382783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50880231 | GACCAGCCAAGGAGC[C/T]GATATTCATGTCTTG | 11124 |
rs530387234 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50449735 | CCTCCTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 11124 |
rs530393767 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50563036 | TAAGTAATCTAGAGA[C/T]GACTCAAAGTAGATG | 11124 |
rs530396030 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951150 | AAGGCAGGAGAACTG[C/T]CTGAACCGGGGAGAT | 11124 |
rs530396413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50776716 | TTTTAAGATTTAAAA[C/G]AAAAAGTGTGATGTG | 11124 |
rs530396759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923452 | AACAAAAACTTCCAA[A/G]AAAGAGAAGCCCAGG | 11124 |
rs530397695 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50827304 | AATTCTTCTGCCTTG[C/G]GAGGCTGTTAATCTA | 11124 |
rs530403367 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50557861 | AGAAGAAAAGCAAAA[A/T]ACACGATGGCATATA | 11124 |
rs530404078 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50505380 | TCCTCTCCAAAATGG[A/C]AGCCTTGTTATGTGG | 11124 |
rs530421203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50871414 | GAGAAGTCAATGCCT[A/G]GCTTCAAAGCTTCAA | 11124 |
rs530422071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50959560 | AATCCCATTCAACCC[A/G]TACTTAACACATTCT | 11124 |
rs530433937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820347 | AGGCTTAATGGGGTA[C/T]AACTGACAAATAAAA | 11124 |
rs530446435 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50727867 | ACTCTTGGACTTACA[C/T]TAGTGGTTTGCCAGG | 11124 |
rs530468351 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50763569 | TTTATATTTGCCTAG[A/C]AGTCGTTCAGACAAC | 11124 |
rs530476236 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50772187 | TGAAAAATAAATAAA[C/T]AAATAAATAATAGAT | 11124 |
rs530477013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50812720 | CCACCATCATTACTG[C/T]GTATATACCCAAAGG | 11124 |
rs530481917 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960538 | CTCACGTGGTTAGTC[A/T]CACAAATACACACCA | 11124 |
rs530495764 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50915350 | ACTCCAGCCTGGGCA[A/T]CAAGAGCGAAACTCC | 11124 |
rs530505857 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50545106 | ATTTTCTGAATTCCA[A/G]ACCACAAAAAAGAGG | 11124 |
rs530509326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50442232 | ATGGGACATGAAGGT[C/G]TTCTGAATCTGCGAG | 11124 |
rs530509775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607474 | CCTTTCCAGCCATTA[C/G]CTCCCACTATTTTTG | 11124 |
rs530511664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875729 | GTGCTGGGATTACAG[C/G]TGTGGGCCACTGCAC | 11124 |
rs530519300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50867256 | AACATTGGAAAAACT[A/G]TTCTTGACATTGGCT | 11124 |
rs530529657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457575 | CAGATTAGATTGTAT[A/G]TACAGCCTTCAAAAG | 11124 |
rs530534800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50805603 | CAAGTCACTGGTAAA[C/T]TGGTAGATTACAAAA | 11124 |
rs530536067 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961759 | GCTGGCTTCCAACTC[C/T]TGTGCTCAAGCCATC | 11124 |
rs530536199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952724 | TCTGCCCCGCCACCC[C/T]GTCTGGGAACTGAGG | 11124 |
rs530552707 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676164 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCCA | 11124 |
rs530560471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510781 | CTTTTTTTTAAGGAC[A/G]TACATAAATGAGTAA | 11124 |
rs530567148 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50811999 | ATGGTGTTGGGGTAG[C/G]TGGTTAGTCATATAC | 11124 |
rs530567565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50844228 | TTTTAAATCATAGTA[C/T]TTGTTTTTCTGCAGT | 11124 |
rs530574718 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50786479 | AAAGTTGCTATCCAA[C/T]GGGTACAGAGTTTCA | 11124 |
rs530578185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50929267 | TTCTTTCATCATTCA[C/T]ACAATTTATACATAG | 11124 |
rs530581850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50524021 | CTAACAGTGTGTAAG[C/T]GCTCTCTTTTCTCTG | 11124 |
rs530584354 | snp | C/T | 0.000133522 | 0.00816966 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788197 | GGTATGGTCTCACCT[C/T]CATATTCACTAAAAT | 11124 |
rs530585673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660423 | TCAGGTATTATTCTC[A/G]TGAAAGCAAACTAAT | 11124 |
rs530599510 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50889173 | GTTTACAGTATTCTC[C/T]GATGGTAGTTTGTAT | 11124 |
rs530606706 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50937705 | CACTGGAGCCAAGTT[C/T]TATATTCCTTTATTG | 11124 |
rs530607819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50590913 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 11124 |
rs530610423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50615512 | TGTAAGTGCTCCCTT[C/T]TCTATGCAGTCTTGC | 11124 |
rs530612534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50574052 | AATTGCTTGAAACTG[C/G]GAGGCAGAGGTTGTA | 11124 |
rs530613372 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FAF1 | GRCh38.p7 | 1:50861390 | TAGAATCTTCATGAT[A/G]GGATTAGTGCCCTTA | 11124 |
rs530613537 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50637353 | AGCTACTCGGGAGGC[G/T]GAGGCAGGAGAATCG | 11124 |
rs530616225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909341 | CTTTGGTGAATCTGA[C/T]AATTATGTGTCTTGG | 11124 |
rs530634226 | in-del | -/ACAGAC | 0.0178098 | 0.0926698 | intron-variant | FAF1 | GRCh38.p7 | 1:50779988 | CACATGCACAGACAG[-/ACAGAC]ACACACACACACACA | 11124 |
rs530635781 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50821348 | TCATATTTTTTTACA[A/G]GCTCCTCAAATGATT | 11124 |
rs530660184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909803 | CAAGGTTTTTAGCTT[A/C]TTTGCGATGGGTTTG | 11124 |
rs530660333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757424 | ATTTTAAATATTTCA[A/C]ACTCTGTTATTAGAT | 11124 |
rs530660827 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50940037 | TGCCTCAGCCTCCCG[A/T]GTAGCTGGGACTACA | 11124 |
rs530663034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50580919 | TGGGACTAGAGGCAT[A/G]CATCACCAGGCCTGG | 11124 |
rs530672210 | in-del | -/TTGT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50757040 | TTATTTAGGAATATG[-/TTGT]TTAATTTCCAAATAT | 11124 |
rs530672935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50637020 | ATATGGATCTATTCC[C/T]GAACACTCTATTTTA | 11124 |
rs530683926 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50619219 | TCTTTTAAGTGAGGC[A/G]TTTAGCCCATTTATA | 11124 |
rs530690324 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50926592 | TTAAATGTTCTCAAC[-/A]AAAAAAAAAAGTTTA | 11124 |
rs530690777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50834282 | AAGCCAATTAAATTT[C/T]GTTTCTTTATAAATT | 11124 |
rs530694707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779591 | AGAAAATTATATATA[A/G]AATACTCTATAAAAT | 11124 |
rs530699799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50930744 | GGAGGTGGAGCTTGC[A/G]ATGAGCCGAGATCGT | 11124 |
rs530699977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50826979 | AGGAGTGCCTCTGCC[C/T]GGCCGCCCATCGTCT | 11124 |
rs530700872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50743367 | GGGTCTCACTCTGTC[A/G]CCCAGGCTAGAGTAC | 11124 |
rs530701205 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50734663 | GGCGTGAACCCAGGG[A/G]GCGGAGCTTGCATTG | 11124 |
rs530705418 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50900674 | AACAAGCTCACAGCA[C/G]ATGCTCAGTAAGTCT | 11124 |
rs530706309 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688216 | GTATTGGTTAGTACA[C/G/T]GGAGAAATGGAAACT | 11124 |
rs530732782 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50720269 | CTCCCAAAAAATGAG[A/C]CACTTTTAAGTGGCC | 11124 |
rs530737046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50517260 | TTATAAGATAACTAT[C/T]TAATTTGAATTAAGA | 11124 |
rs530739911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50583569 | AGGAGAAACTTTAAA[C/T]AATCTATAATTAAAA | 11124 |
rs530742858 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50526744 | TACATTTAATCAACT[G/T]AAGAGCTGCCAGACT | 11124 |
rs530743870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674100 | GGGTTACAGGCGTCC[A/G]CCACCACACCCAGCT | 11124 |
rs530752021 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50456796 | CAGAACAGTAAAGGG[A/C]CACAAGAGGGAAAAG | 11124 |
rs530759479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50628667 | TGCAACTAAAAGAAT[C/T]GTCAAACAGGTGCAC | 11124 |
rs530760051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674986 | ACCTCCGCCTCCTGG[G/T]TTCAACCAATTCTCC | 11124 |
rs530766800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50637997 | CTCCAATTATTTGCC[A/G]TTTTCAATGTATAGA | 11124 |
rs530772189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836764 | TTTTAAAAGAAAGTA[A/T]ATTGCAAGCATTATG | 11124 |
rs530792843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50737043 | TAACTTTTACATTAG[C/T]AGGAGTCTCCATTTG | 11124 |
rs530794277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621743 | TACCTGGGGCCAGCA[C/T]CTCCTAGAGGAAGAT | 11124 |
rs530795905 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50883737 | AAAGCTGTAAAAAAA[A/T]TTTTTTCAGCATAAC | 11124 |
rs530797240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50885398 | GCATATATATTCACA[A/G]TTGTTATGGCCTCGC | 11124 |
rs530797889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50629357 | GTATTTTAATAGAGA[C/T]AGGGTTTCATCATAT | 11124 |
rs530802460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510056 | CACCTGTAGTCCCAG[A/C]TGCTCAGGAGGCTGA | 11124 |
rs530807910 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681357 | TGGCCTAATTAACTT[C/T]TATCACTTAACTTTT | 11124 |
rs530815740 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50897347 | GAGGAGAGTGTGATT[A/G]TCTGTTCCCACAATT | 11124 |
rs530818387 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50922913 | ATGAGACTAACAAAA[A/G]AAATTCAGAAATGAA | 11124 |
rs530818750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50518083 | CGAAACAGTTTCATC[A/G]TACAAAAAATATCCC | 11124 |
rs530827064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50477077 | AAAGTTTGCTCAGAC[A/G]CAAGTATGGATAAGA | 11124 |
rs530827347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467783 | TACCTAACCTCTTTT[A/G]TGCCTCAGTTTCCCT | 11124 |
rs530850681 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50615869 | TTAATTAGGTCCTAC[C/T]TGTCAATTTTTGTTT | 11124 |
rs530850977 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50651123 | CAAGATTATAAAAGA[A/G]TTGATTACAAGAGGT | 11124 |
rs530855958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50524931 | TGCTCTGTTGCCCAG[G/T]GTGTAGTGCAGTGGT | 11124 |
rs530859812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50828274 | CTTTTTTTTTTTTTT[C/T]CTTTCTTTTTTTGAG | 11124 |
rs530862157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721743 | ATCCTTCCATCTCAG[C/G]CTCCCAAGTAGCTAG | 11124 |
rs530865489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50729602 | AGTAGAGACAGGGTT[C/T]CACCATGTTGGCTAG | 11124 |
rs530879188 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750587 | TGGGTTCCTTTGTTT[A/G]GAGTAATGTTTTCGA | 11124 |
rs530879611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876671 | GCTCACAGCAACCTC[C/T]GCCTCCCAGGTTCAA | 11124 |
rs530883723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50623844 | ACTACCCAAGAAGCT[G/T]AAGTGGGAGCCCAGG | 11124 |
rs530884527 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50956042 | AACAGATTTTCAAGA[G/T]GAAAAGCTTTCTGGA | 11124 |
rs530884659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773562 | ATTCTGCTAAGTGAA[A/T]TAAGACAGGCACAGA | 11124 |
rs530889036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512767 | TTTTTTCTAATTCTG[G/T]GAAGAAAGTCAATGG | 11124 |
rs530900523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50683306 | TCGATGCAGGTGGAT[C/G]ACTTGAGGCCAGGAG | 11124 |
rs530900934 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50513983 | CAGCGCAAATACAAT[A/C]CTTGAATTAGGGTAG | 11124 |
rs530902074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940770 | GTAAAAGTGACGTAA[A/C]AATACTAGTAACTAC | 11124 |
rs530906049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50585694 | ATAAATATTACTTAG[C/T]AAATAAAATTTCTAT | 11124 |
rs530916612 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50929498 | AAATTTTACACACTG[C/T]TTATATTATATCTTT | 11124 |
rs530921180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624306 | GTGCCAGCCACCACG[C/T]CCAGCTAATTTTTTG | 11124 |
rs530939064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459863 | TCAATTTGTATAAGC[C/T]GCTTGGCAGCTCTAA | 11124 |
rs530939719 | in-del | -/T | 0.00282942 | 0.0375061 | intron-variant | FAF1 | GRCh38.p7 | 1:50583398 | CCTTTGGGAATATAA[-/T]AAAAATATTAAATTA | 11124 |
rs530970436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50600356 | ACAGTGATTGCATGA[C/T]GTTATAAAATTATGT | 11124 |
rs530970778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50924769 | GGGTGGATCACCTGA[A/G]TTCAAGAGTTCAAGA | 11124 |
rs530981557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50837308 | CTACTTGGGGATCAC[A/G]CATTGTTGTATTTAG | 11124 |
rs531006492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850993 | TAGAAATTAAATCAA[C/G]CTAAATTGTAGGTTA | 11124 |
rs531011000 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50782381 | GGTAATGTGTGTGTT[C/T]GTGTCTTAGTTTTTA | 11124 |
rs531014105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744282 | TCTTTGTTCCATAAT[C/T]AATACTTGACATAAA | 11124 |
rs531015710 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458148 | AACCTGGGAGGCAGA[A/G]GTTGCAGTGAGCTGA | 11124 |
rs531027686 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50457044 | ATCTCAGTTTTTTCA[C/T]CTAGAAAATAGGTTT | 11124 |
rs531030579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50646048 | CTTCATATGGTCCCA[C/T]CTAATAATATGTTAA | 11124 |
rs531036967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50485641 | CACCACTGCACCCCA[A/G]CCTGGGCAACAGAGC | 11124 |
rs531043526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50851415 | AAGTCGTTAAGCAGC[A/G]TATGCTACTTCTTTC | 11124 |
rs531050293 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50722370 | AGAGCACTATAAGGC[C/T]GGGCGCGGTGGCTCA | 11124 |
rs531055067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50947416 | ATTCTTCCTATCTCT[A/G]TTATTCCCCCATAAC | 11124 |
rs531058326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50519277 | GAGGTTGCAGTGAGT[C/T]GAGACCACGCCACTG | 11124 |
rs531060497 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50510114 | GGGGTTGCAGTGAGC[C/T]GAGATGGCACCACTG | 11124 |
rs531064022 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50775673 | TAGAAAAGATGGACT[A/G]AAGGAAGAAAGAAAC | 11124 |
rs531067293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50813766 | TTAACACTGTATTGT[C/T]GGCATCTCTCCATAC | 11124 |
rs531069383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896743 | AAAGTAGTAAAACTC[C/T]TAGAGACAGAAAATA | 11124 |
rs531072320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50774608 | TTCAAATAATAACAG[A/G]CCTATTTTTCTGCTA | 11124 |
rs531074613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459702 | AATTTTCTAGTGCAA[C/T]AGTCATATCTGGTCT | 11124 |
rs531075339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50677131 | TAAGATAAACCCATA[A/C]ACAAAGAAAAATGGG | 11124 |
rs531091586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543253 | TTCACCAAGCTATAC[G/T]CTAACATAAAATATA | 11124 |
rs531093550 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50535131 | GACTTCCTGTACCCA[C/T]CCCAAATCTAGCAAA | 11124 |
rs531099728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50615817 | TATGTCATTTACTCC[A/G]TCAATAGTTTATTTT | 11124 |
rs531110362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526250 | TTGCCTACCTTGGCC[G/T]GCTCATGGTGGCATG | 11124 |
rs531116200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939894 | ATTACAGTATGTCAA[C/T]AAAAGTACTTTTTTA | 11124 |
rs531122966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50652532 | CTGTGAAGCCCCACA[G/T]TTCCAGAGTTTCTCT | 11124 |
rs531128497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860190 | CATTCTGGACATCAA[C/T]CTTGGCAAAGAATTT | 11124 |
rs531131632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50542361 | CAAATCTTTCTCATG[A/G]CTAGGAGACTCTGCT | 11124 |
rs531132248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844764 | TATGAGATGGTGTGA[A/G]AAAAGAGAGGTACCT | 11124 |
rs531135141 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751686 | CCTACTTGGCTATGA[G/T]GTATACTATAAACGT | 11124 |
rs531147811 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50778673 | TGAACAAACTGAAGA[A/G]AAGGAGGAAGGGGAG | 11124 |
rs531155589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896075 | GGAAACAAATAAAGG[A/G]TATCCAAATTGGAAA | 11124 |
rs531159461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50797053 | ATGTGGGAGGATCAA[C/T]TGAGTCAGGGAGGTA | 11124 |
rs531163931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50806455 | CAGGTAAACATGTGA[C/T]GGAGGCAGCCGACAC | 11124 |
rs531169186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50530919 | TTAAACAAAGGAAAG[A/G]AAAAGGAATGCACTG | 11124 |
rs531178081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50589315 | GGGGAGGAGGGATTT[C/T]AGGTGCTTAGGCACC | 11124 |
rs531182036 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50689823 | CCATTCTATTTTCTG[A/T]TACTTTATTTTAGAA | 11124 |
rs531185848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50471885 | AGAAGAGTTGTGGGA[C/T]AAAGAAATAAGGAGA | 11124 |
rs531198890 | snp | A/C | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50642896 | CCCAGGTTAGAGTTC[A/C]ATGGCACGATCTTGG | 11124 |
rs531200318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744859 | GCTAACACTAATATG[G/T]GGCATACAGTGTACA | 11124 |
rs531203123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50634448 | CGTATCACATATGTT[A/G]CAGCTGTTCAAATGC | 11124 |
rs531214164 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50532851 | GGGTCTCACTCTGTC[A/G]CCCAGACTGGAGTAT | 11124 |
rs531221891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50481571 | TCTATGTTTGTGTAA[A/G]TAAAGTCTAGGATGT | 11124 |
rs531222942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50797802 | CTTGAGCTCAGGAGG[A/C]GTTCAAGTCCAGCCT | 11124 |
rs531226148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893453 | GGTATTGCCTTGATG[A/G]TCTTGGATAAGATCT | 11124 |
rs531226355 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50851437 | ACTTCTTTCAGAATT[A/G]GCATGAAGCCTCTAA | 11124 |
rs531228972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50535307 | GCATGTATCATCATT[C/T]GACAAATTAAAATCC | 11124 |
rs531233980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50697271 | GCATACAGGGACACT[C/G]TAATACTTAGCCATG | 11124 |
rs531237044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50790245 | CTCCTGGGTTCAAGT[A/G]ATTCTCCTACCTCAG | 11124 |
rs531239772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50635531 | CCCAGGCTCCAGCAA[C/T]CCTCCCACCTCAGCC | 11124 |
rs531253063 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50841237 | TAAATGCCCTTGACA[C/G]ATATATATAAAATTT | 11124 |
rs531261742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50888094 | GAAGAGGTCCTTCAC[A/G]TCCCTTGTAAGTTGG | 11124 |
rs531264943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50733712 | CTCTACTGGAACCTT[C/T]ATCTTGGAGATTTCC | 11124 |
rs531268108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534754 | TTAGCACAGTGCCTA[A/G]CACATGATAAATACT | 11124 |
rs531276105 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50626853 | GGGTAGTGGCAGTGG[A/G]AATAGAAGTGAATGA | 11124 |
rs531293119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50920943 | AATAAAGTAAGAAAA[A/G]GAAAGAAAAAGTCAT | 11124 |
rs531298021 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50935670 | TAGAGATGGGGTTTC[A/T]CCATGTTGGCCAGGC | 11124 |
rs531302859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50785838 | CTATGAAATATCCAC[A/T]CTCCCATGGCTGGGC | 11124 |
rs531306591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50686295 | TACCTGTAATCCCAG[C/G]ACTTTGGGAGGCCAA | 11124 |
rs531319806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725642 | TGTATTTTTAGTAAA[A/G]AAGGGGTTTCGCCAT | 11124 |
rs531320614 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50450071 | GTGGTGGTGCACACT[A/G]TAATCCCAGCTACTC | 11124 |
rs531327188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807327 | TTTAATTGACTCACA[A/G]TTCCACAGGCTGTAT | 11124 |
rs531328113 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642423 | TGGGAGGCCGACGCG[G/T]GGGGATCACAAAGTC | 11124 |
rs531329461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50522391 | CTCCTCAGTAAATGG[C/G]GGCAATTACTATCTC | 11124 |
rs531344218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50769296 | GTGAAATTGAATGAA[A/T]AATAAAAAGCCTACC | 11124 |
rs531348928 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50503203 | ATTATCCTATTAACA[-/CT]GTTAATAATTGCTAA | 11124 |
rs531360943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50936383 | GAGGAGGGAGTAAGT[A/T]ACTGTCAGAGAAGAC | 11124 |
rs531365072 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50889082 | TCAGCTTCTTCCTGG[C/T]TTAGTCTTGGGAGGG | 11124 |
rs531368282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579939 | ATATTAGAGAATTAT[C/T]GTTAATTTTGTTATA | 11124 |
rs531370811 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50949646 | GACAACATGTAAACA[G/T]ACGTGCACGACTATA | 11124 |
rs531382356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50832463 | CTGGGCTAGTAAGTG[C/T]CAATAGCACCCTCAG | 11124 |
rs531385025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949660 | ATACGTGCACGACTA[C/T]ATTCCAGTAAGACTT | 11124 |
rs531387707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50665090 | AATCAAGTAAATTAA[C/T]CAATTTATAATTCTT | 11124 |
rs531390305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50572839 | ACATCAGATTGGCTG[C/T]TTCTTTATGAAGATG | 11124 |
rs531391614 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50719490 | AACATTTTTCATGAT[G/T]ATTTCAAAGTTCAGG | 11124 |
rs531397200 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462280 | AACATTTTATATCGA[-/T]TTTTTAAATGCTCAC | 11124 |
rs531401486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50863468 | AAACTAGAGAAACAA[C/G]AAGAAAACAAACCCA | 11124 |
rs531402338 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50670340 | CAATCTGCCTACCTG[C/T]ACCTCCCAAAGTGCT | 11124 |
rs531410756 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50582239 | CCTTTTTTCCCATTT[-/A]AAAAAAAAACCCTAT | 11124 |
rs531413846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50553711 | AAAGAACTAATTATA[A/T]TTGGTAGGAAGAGGC | 11124 |
rs531416567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50446286 | CTCTTTCTAGTCACA[C/T]CCTTCTGCCTCTCAC | 11124 |
rs531419122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824632 | ATACATCCAAAGAAG[A/C]GATAGTTGCACTCCT | 11124 |
rs531422231 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50451654 | CCCATAACAGAGTGT[A/G]TTATTACCTTAGGCA | 11124 |
rs531428191 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50899474 | CTGTATTCCTTTAAA[C/T]ATATATATTTTGAGA | 11124 |
rs531435990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50809145 | GAGAAAAGTTTATAG[C/T]GCTGAACACCCACAG | 11124 |
rs531442125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50847055 | AATCTGTGATACAAG[C/T]GGATCATTCTTGATT | 11124 |
rs531443009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620172 | TCGGCCTCCCAAAAT[A/G]CTGGGATTATAGGCG | 11124 |
rs531454666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50480495 | ATTCCATGAATTCTT[A/G]CTGAGCATCTTCTAT | 11124 |
rs531460371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649601 | GTTTCTCAATTCTGA[A/G]TGAATATTTTGTGGC | 11124 |
rs531461759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50680364 | CTTAGAAATATAATA[C/T]TCTCCCATATTATTA | 11124 |
rs531465661 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50847958 | AACACAAAGAAACAT[C/G]TTAAAAAAGGCTGTC | 11124 |
rs531481262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50672439 | GGGTATCACCCAGCT[A/C]ATTTTTGTATTTTTT | 11124 |
rs531486933 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50920227 | AATCGCTTGAGCCTG[A/G]GGGGCAGAGGGTTGC | 11124 |
rs531493607 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50487010 | TTTACTATATTGTAC[C/T]TTAGCCTTATGATTT | 11124 |
rs531496402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50701074 | TAAAAGATGCATAAT[C/T]GTCTTTTCTGAAAGC | 11124 |
rs531497444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50595877 | CTGATGGTTCTAAGT[A/G]AAAATCATTTCAACC | 11124 |
rs531508769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50546405 | GAGTCTCACTCTGTC[A/G]TCTAGGCTGGAGTGC | 11124 |
rs531515049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50656054 | AAGTAGCACAGGGCC[A/G]GGGACGGTGGCTCAC | 11124 |
rs531532292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50839218 | ATTTCATTTCTACTA[C/T]TATTTTTACAAACAA | 11124 |
rs531532925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50596367 | CCAGGAAGGCTTTGA[A/G]AATTTGAAATTTTTC | 11124 |
rs531536039 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50887319 | AATTTTCTCCCATTC[A/G/T]GTAGGTTGCCTGTTC | 11124 |
rs531544356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50692711 | TACATTGCTTCCATA[C/T]CTTGCTTATTGTGAA | 11124 |
rs531545475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545785 | CTTAAACAAGCATTT[A/C]GTCTATAGATATATT | 11124 |
rs531548598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50670432 | GCTAGTAGTGACCCT[A/G]TTGGACAATATATTG | 11124 |
rs531558460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906686 | CTCTCTGTTTGTCTG[C/T]TATTGGTGTATAGGA | 11124 |
rs531564766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50800631 | TCATCTAAAAACCAT[C/T]AACCATTAAAGGTGG | 11124 |
rs531569762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50540735 | AAAAAGTAAATGTCA[C/T]AATAATAATGAATTA | 11124 |
rs531573439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562509 | CACCCAAAAGACTAG[C/G]AATGCTACTATGGTA | 11124 |
rs531577888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650439 | AGCCTGGCCAACACA[G/T]CGAAACCCTGTCTCT | 11124 |
rs531578906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50942649 | CAACCTGGCCTGTTA[A/C]AATTTCATGGATATT | 11124 |
rs531585392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50736311 | TCTAAGAATCCATCA[A/G]TTGTAACAAAATTCT | 11124 |
rs531588580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50642379 | TCTTGGGCCAGGCAC[A/G]GTGGCTCACACCTGT | 11124 |
rs531592738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50900404 | TTGCAATGGTGATTA[C/T]TGTTTTCTTCTTAAT | 11124 |
rs531596562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50755919 | CTAGGCTGCACACAG[C/T]ACAGGGACCCTGGGT | 11124 |
rs531599999 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50526969 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCTAAGTA | 11124 |
rs531608715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749586 | AGCTCAGAAGTTTGA[A/G]ACCAACATGAGCAAC | 11124 |
rs531614415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650848 | GTAACTCCTTGTTCT[C/T]ACAGCTGAACTGTCA | 11124 |
rs531614812 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50483280 | TTCCCCATTGAATTG[C/T]CTTTGTATCTCTGTT | 11124 |
rs531629573 | snp | A/C/G | 1.65397e-05 | 0.00287569 | intron-variant | FAF1 | GRCh38.p7 | 1:50801698 | AACAAGAAACAGAGA[A/C/G]GGCCATTTAAAGAAA | 11124 |
rs531632400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50530294 | GTATATATGTATATA[C/T]GTATGAGTGTGTGTG | 11124 |
rs531635872 | snp | C/T | 1.83353e-05 | 0.00302776 | intron-variant | FAF1 | GRCh38.p7 | 1:50539745 | TAAAAGGAGACAAAA[C/T]ACAAAGTAAGTTTTG | 11124 |
rs531639122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943499 | ATTTTATCATCCATA[A/G]TAACTCTTGTCAGTG | 11124 |
rs531651967 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50952297 | ATCTTTTTGGTGGAG[A/G]CGGGTTTTCGCCGTG | 11124 |
rs531652357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50903504 | AAGGAATTAAATGAT[A/G]TATCTTTAGTATATG | 11124 |
rs531659472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847641 | GTCAGAATCTTAGAA[A/C]GAGGAGAGAGAAAGA | 11124 |
rs531664904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588359 | TCTAATTCTTTAGGG[A/T]CAGTTACTAGAGTTT | 11124 |
rs531673018 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50560222 | TATGGCTAATTACTG[A/G]GATGGAAAGTACATG | 11124 |
rs531673599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50538906 | AGGCAGAAATTAGTA[C/T]ACCAGATATAGTTTT | 11124 |
rs531679263 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50916809 | AGGACAGAATTAATG[G/T]CAATAAGTAAGTAAA | 11124 |
rs531695058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50606690 | TATTTTAGTAGAGAC[A/G]GAGTTTCTCCATGTT | 11124 |
rs531696457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50796125 | AAAACAGGGAATACA[A/G]AATAAATAGTGAAAG | 11124 |
rs531698170 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746209 | GCTTCTAGTACCCTA[C/T]GCTCGTATGTGTGAG | 11124 |
rs531715417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770891 | GTAACCATAACAGCA[C/T]GTTACTGGTATAAAA | 11124 |
rs531721505 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50927597 | AGTTTTAAAACTGGC[-/A]AAACTAACATATGTG | 11124 |
rs531725738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50483592 | GCAAGTTTTTGAAGT[A/G]ACATGATGTGACAAA | 11124 |
rs531728539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50532701 | AGCAATAGAAGATAC[A/C]TAGTGAGCATTAAAA | 11124 |
rs531733739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50857464 | GCCTTTTGATTACTG[C/T]CAAAAAAGAAAAAAC | 11124 |
rs531746486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50590950 | TCGTGCCACTGTACT[C/T]CAGCCTGGGCAACAG | 11124 |
rs531757930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895262 | ATAAATTTGAAAACT[C/T]AGACCAAATGTGGCA | 11124 |
rs531789202 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50802132 | TTTCACTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 11124 |
rs531790950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50484520 | ATTGAATTGTAAAAA[C/T]TCAATAAGATAATTA | 11124 |
rs531806145 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50742471 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGC | 11124 |
rs531810438 | in-del | -/GTAAGG | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50909103 | AGCATTTGCTTGTCT[-/GTAAGG]GATTTTATTTCTCCT | 11124 |
rs531812089 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50761537 | GGCTGGTTCAATATA[C/T]GCAAATCAATAAATG | 11124 |
rs531812865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50454996 | TCCCTAGAGCCTCCA[C/T]GAATTCAAAGAAATG | 11124 |
rs531816395 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50454605 | TACCTTTATTTCACC[C/T]TAGGATCCTCAGACA | 11124 |
rs531821390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922091 | GAATTGCTTAGAACC[C/T]GGGAGGCAGAGGTTG | 11124 |
rs531826001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50507134 | TTCATACTGGACACA[A/G]GGCAGGGCACTTAGT | 11124 |
rs531827344 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50516448 | TATTACCCTGTATAC[C/G/T]TTGGCTTGGACTTGT | 11124 |
rs531829443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50590364 | CAAGTCTCCCGCTTC[A/T]TTTATTAGTTAATTC | 11124 |
rs531833639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50787524 | ACAGTGAGCAGCCCT[C/T]ACCAGACATCAAACC | 11124 |
rs531835185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598226 | ACTTGAGCCCAGGTG[A/G]TTAAGGCTGCAGTGA | 11124 |
rs531855493 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909916 | ATCCAGCTTTGTTCC[A/G]TTGCTGGTGAGGAGC | 11124 |
rs531871776 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50726462 | AGCACTTTGGGTGGC[C/G]GAGGCGGACAGATCA | 11124 |
rs531877729 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50888687 | ATTTGCGTATGTCGA[A/T]CGAGCCTTGCATCCC | 11124 |
rs531879422 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50498843 | CGACAGAGCGAACCT[C/T]TGTCTCAAAAAAAAA | 11124 |
rs531879822 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50805987 | TGTCACAACAATGGG[C/T]AGGCAAATGATGAAA | 11124 |
rs531882465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50907481 | TCCTTGTACCTCTGG[C/T]AGAATTCGGTTGTGA | 11124 |
rs531887864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50656456 | CCTTCCTGAAAATTA[A/G]ATACAAAAAATGCAT | 11124 |
rs531892432 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50635674 | CAGGCTGGTCTCAAA[A/C]CGCTAAGCTCAAGCA | 11124 |
rs531899130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50613073 | ATGCTCTAACTTATA[C/T]GGGTACTTTTCCTAC | 11124 |
rs531900937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50802945 | TCGTACTGTTGAATG[A/G]AAATAAATAGAGTGT | 11124 |
rs531902645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447151 | TTTTTTTTGAGATGG[A/G]GTCTCCCTCTGTTGT | 11124 |
rs531906137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921403 | ACAACAAGACCAGCT[A/C]TACAAGAAATGTTTA | 11124 |
rs531913092 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50825296 | ACAAACCTTAAATAT[A/G]AAAACCTAAAAATGT | 11124 |
rs531916937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50554962 | ATCTGTCTGTCTGCA[A/C]AAACAATGAGAAAAC | 11124 |
rs531918262 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50762654 | GTAGAAAGCTGAAAC[C/T]GGATCCCTCCTTACA | 11124 |
rs531920912 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50455557 | TTTGTTCTAGTTTTC[A/C/G]GAAGAGAGTTGTCAA | 11124 |
rs531921689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50865980 | ACCAAATCCAACTGC[A/G]TATCAAAATGAGAAT | 11124 |
rs531922592 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50657671 | GTTGTCCAATTATAG[C/T]ATTTTGTTTTCACAT | 11124 |
rs531923472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50564032 | TGATACTCATATTCT[C/G]GTGACTTCATCAAAG | 11124 |
rs531928024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810886 | AGACCCCGTCTCTAC[C/T]GAAAACACAAAAATT | 11124 |
rs531937138 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50835467 | AAATCATTTAACAGG[A/C]GGCTGAGGCAGGAGA | 11124 |
rs531938828 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50613925 | AACATAGTGAAACCC[G/T]GTCTATACTAAAAAT | 11124 |
rs531943912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50913785 | GGAACTGATGGATGA[A/C]TATCCAAACAGCAGA | 11124 |
rs531951140 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50642122 | GCACGAGAATTGCTT[A/G]AACCCTGGAGGCGGA | 11124 |
rs531952822 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50911470 | GGAGGCCAAGGCAGG[C/T]GGATCACTTGAGGTC | 11124 |
rs531955261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50544186 | TTCCCATATGAGTTT[C/T]GGTGGGGATGCTCAA | 11124 |
rs531974153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50697682 | TGTAAAACCCTAGAA[C/G]AATCCAGTACTCTAC | 11124 |
rs531986291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551712 | AAGGCATATAATAAG[A/G]TGTTCCAAAAGATCC | 11124 |
rs531986713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50810473 | ATCCATAGCCAACAT[C/T]ACACTGAATGGGCAA | 11124 |
rs531987655 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50551054 | TACAGCTAAACTTCA[A/T]CTCAGGTGCTTATAA | 11124 |
rs531988431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50953856 | TGTGTTACAGAAAAC[A/G]TAACTGAAAATAACA | 11124 |
rs531997748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50818857 | CAAAAAAAAAAAAGA[A/G]ATCTTGGAGATGGGA | 11124 |
rs532003512 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50864713 | ATTAAAGACTTAAAC[A/G]TTAGATCTAAAACCA | 11124 |
rs532009166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50797995 | AACAGAAAGAAAACT[A/G]AACAGGAACTCTGCA | 11124 |
rs532012542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807141 | ATAAAAGGATTCTAA[A/G]GAATACAATAAAATA | 11124 |
rs532022565 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499735 | CCCTTCCCTCCCCTT[C/T]CTCCCTTCTTTCTTT | 11124 |
rs532027960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50646961 | AGCAATTCTTGTGTC[C/T]CAGCCTCCTGAGTGT | 11124 |
rs532028455 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50576640 | TCCGCACCGCCCCCC[C/G]CCCGCCACCACCCCT | 11124 |
rs532031839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50710845 | CTGACCTCGTGATCC[A/G]CCCATCTCAGCCTCC | 11124 |
rs532037257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50498022 | AAACTTACTATAAAG[C/T]TACAGTAATTGAAAC | 11124 |
rs532037569 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50912256 | CGGTGTTGTCCTCAT[C/T]CTTCCTACATCAGAT | 11124 |
rs532050838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50856374 | TTGGGAGCATCGTTT[C/T]GATTAAGCCACTGCT | 11124 |
rs532057360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50664572 | AAGGTGGGTGGATCA[C/T]GAGGTCAGCAGATCG | 11124 |
rs532059950 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50549461 | CTACAGGCATGCACC[A/T]CCATGCCCAGCTAAG | 11124 |
rs532066805 | in-del | -/AAATGGTAACACCCAGTTTTAAAGA | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50504636 | CCCAACATCAATTTC[-/AAATGGTAACACCCAGTTTTAAAGA]AACTCCTAAACTGAA | 11124 |
rs532069375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447634 | GCAACCCTTTGCCAC[A/G]CTGGCAGAAAATCTG | 11124 |
rs532081223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941019 | ATACTTGGATGCAGT[C/T]TGGGGTTTTTTTGGT | 11124 |
rs532084892 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50664418 | CTCACTAAATAAACT[C/T]GGAAGATATCTATAT | 11124 |
rs532088653 | in-del | -/GTT | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50737876 | CAAAAAAATCACCAA[-/GTT]GTTGTATTTAAAAGA | 11124 |
rs532090595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50690600 | AGCAAGACTGTCTCA[A/G]AAACAAACAAACAAA | 11124 |
rs532103329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50593124 | ATAGGAGGGCAAAAC[G/T]CCTAATAATAAGATA | 11124 |
rs532107900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50544797 | AAAGTCTCAATGAAA[C/T]GCTGACATTTGATCA | 11124 |
rs532116981 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894003 | AGGGACTACTGCCAG[G/T]CTACTGCCAATGTTC | 11124 |
rs532118027 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50779494 | GCTGCAGAACTGATA[C/G]TGTGTTAGCAGGCGG | 11124 |
rs532127212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845937 | AGAACAACCTGGCCA[A/G]CATGAGGAAACCCCG | 11124 |
rs532136043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50764515 | TTAACTCTGCAGGAC[C/T]GTTGGGCTCTGCTTA | 11124 |
rs532136617 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50752416 | TGTAAATTTACCAGC[A/G]TAAGTTTGTTCTTAA | 11124 |
rs532139038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851583 | AGCCACATTTCCAAA[C/T]TGCATTCAACCATGG | 11124 |
rs532143814 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50535726 | TAGCACTATATAGAA[C/G]AATGTCCAAATCATG | 11124 |
rs532143871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50668479 | GGCAGAAAGCCTATC[A/T]TAAGAAAAGTAGCTG | 11124 |
rs532148828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50443426 | TAAAATTTCTTGAAC[A/G]CCTACTATATGCCAG | 11124 |
rs532171036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707709 | AAAAAAAAGAAAGAA[A/G]AAAGAAAAGAAAAAA | 11124 |
rs532179525 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50536086 | ATCCTCCAGTGAAAG[A/C]AATAGTAATTCAATT | 11124 |
rs532181056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50660634 | GAGTAGCTGGGATTA[C/T]AGGAGTGTGCCACCA | 11124 |
rs532186831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50917035 | TATCACCCTAAGAGA[A/G]TCAGCTATCAAAAAA | 11124 |
rs532190373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559060 | GTTCGAGATCAGCCC[A/G]ACCTACAAGGTGAAA | 11124 |
rs532192452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876622 | ATGGAGTCTCACTCT[C/G]TCACCCAGGCTGGAG | 11124 |
rs532217536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50488223 | GCCTGTCCTCTCCCC[C/G]ACTGTACCCCAACCT | 11124 |
rs532227492 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50538204 | AAGTAAAAATAATTT[A/C]TATAAGAAATAAAAA | 11124 |
rs532228438 | snp | G/T | 0.000272403 | 0.0116674 | intron-variant | FAF1 | GRCh38.p7 | 1:50567260 | AAAAATCTGATCAAT[G/T]AAAATATCCACTAAT | 11124 |
rs532237934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602071 | CTATGATCTTCATAC[A/G]TCACTAAGGAGATTT | 11124 |
rs532240775 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50645609 | GCGGGGAGAACCTGA[A/G]GTCAGGAGTTTGAGA | 11124 |
rs532255661 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50884111 | GCCTGGGCAACGGAG[C/T]GAGGAAGTACTTAAC | 11124 |
rs532264231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50593966 | AATGGAAAAAAATTT[G/T]TATCTTACTAGCCTA | 11124 |
rs532270006 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50452096 | TTAGTCTAAAAACAG[A/G]AGATGATCCAAGTCT | 11124 |
rs532271666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909946 | CTGCATTCCTCTGGA[A/G]GAGAAGAGGCACTCT | 11124 |
rs532275502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890733 | TGTCGAGAGATCCCC[C/T]GTTAGTCTGATGGGC | 11124 |
rs532278959 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50814463 | ACAAACCGACTACAG[A/G]TAAATTCAAAAAAAC | 11124 |
rs532279945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512719 | TCTTGGCTATAACGG[C/T]TCTTTTTTGGTTCCA | 11124 |
rs532291590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806650 | GGCCAGAGGATTGGG[A/T]ACATCTCAGAAGCTC | 11124 |
rs532297226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50676502 | ATTATTTTCAATGTA[A/T]CAATCACCCTGGAAT | 11124 |
rs532305749 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50456053 | GCACTCCAGTTTGGG[C/T]GACAGAGTGAGACCC | 11124 |
rs532305766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50766053 | GCCGAGATCGCGCCA[C/T]TGCACTCCAGCCTGG | 11124 |
rs532306430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50706923 | GAATTAGACAGATAG[A/G]ACGGGCACGGTGGCT | 11124 |
rs532310187 | in-del | -/CTT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50911405 | TTTTCTTGAGAAAAA[-/CTT]CTTCCTGGCTGGGCG | 11124 |
rs532315801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50661263 | AACTATTCTATCAAT[C/T]TAATGTCATCAAAGT | 11124 |
rs532329504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50567894 | TCCACTGTGGCTCTT[C/T]ATATAGAAAATTATT | 11124 |
rs532330731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50442498 | AGGTGTTCCATAATG[A/G]CTGCTGTGTGTGAGA | 11124 |
rs532338803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758347 | GCATAAGCCACCACG[C/T]CCAGCACAACATACA | 11124 |
rs532340911 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50919613 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 11124 |
rs532341241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50831152 | TTTTTTTTTAAAGTT[C/T]CTAATTAACAAATAA | 11124 |
rs532341860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669398 | GCACATGGAGAGACA[A/C]TGTCATAGACTGTGT | 11124 |
rs532343185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822943 | CAACACCCAGCTAAT[A/T]TTGTATTTTTAGTAG | 11124 |
rs532343293 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470139 | ATATTAGAGGTATTA[C/T]CATAGGAAGGTTTTT | 11124 |
rs532345357 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50487788 | CTCTTGTTTCTCAAT[A/G]TAATTATATGGGTTA | 11124 |
rs532369814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576538 | GTCTAATGATTCTCC[A/G]GGGTACTTTTGGTGG | 11124 |
rs532372240 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50713359 | GTTCACTGCAACCTC[C/T]GCCTCCCAGGATCAA | 11124 |
rs532377926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919231 | ATAAACAAAAGCTGA[A/G]AGAATTTCTCACCAA | 11124 |
rs532384230 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50870524 | CAAGTCCATCAGAAC[A/C]ATTTTTCCAATAGTA | 11124 |
rs532395227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50715825 | CATTTTTTAAAAAGG[A/G]GAAAATTAGGTATAG | 11124 |
rs532415159 | in-del | -/CCG | 0.0528381 | 0.153711 | cds-indel, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959893 | CGACCGTCGCCGCCA[-/CCG]CCGCCGCCGCCGCCG | 11124 |
rs532417877 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50709950 | TCAGACATAGAACAG[C/T]TCAGAAACGACGATG | 11124 |
rs532421721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616889 | TTTGGCCATGTTGGC[A/C]AGGCTGGTCTCAAAC | 11124 |
rs532428524 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723835 | CTCACTGCAACCTCC[A/C/G]CCTCCCAGGTTCAAG | 11124 |
rs532435914 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50917678 | GGAAAGGAAAGGAAA[A/G]GAAAGGAAAGGAAAG | 11124 |
rs532436554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714204 | TTTTTTTCAATAGAA[A/G]TATTTGCATTATCTT | 11124 |
rs532441563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862505 | GAGGAATAAGATCTC[A/G]TATTTGTTAGCACAA | 11124 |
rs532444155 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50674125 | CCAGCTAATTTTTCT[A/G]TATTTTTAGTAGAGA | 11124 |
rs532448035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50869590 | GCTCCTACTTGCCAT[A/G]GAGGTGCATCTCATT | 11124 |
rs532452614 | in-del | -/GTGTACAC | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50739295 | TATACATATGTACAT[-/GTGTACAC]GTGTACACGTACATG | 11124 |
rs532454665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807993 | GTGAAAGATAAAATA[C/T]TAAAGGCAGCTAGGA | 11124 |
rs532455485 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50712592 | ATCTGGGAGGCAGAG[A/G]TTGCAGTGAGCCGAA | 11124 |
rs532459998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50716375 | ATAGTACTAGGGGAA[A/G]CACTCACTATTATAA | 11124 |
rs532469809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709501 | AAGAACTACTGATTA[C/T]CATTTTTTTAGCCTG | 11124 |
rs532470200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608912 | TGTAAAGTCTTATAA[A/G]TTACAAGATTGTTGT | 11124 |
rs532472287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714839 | GTTCTCAGAGCCCCT[A/G]GGCAGACAGACACAG | 11124 |
rs532477580 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50863097 | GAACATTCTCCAAGA[C/T]AGGTCATATGGTAGG | 11124 |
rs532481481 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50559859 | GACCTGGGATGTTTA[G/T]GATGGCAATACACTT | 11124 |
rs532482681 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50565445 | AACAACACCTTTATT[C/T]AGTGTTTTTAAAAAA | 11124 |
rs532485085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50619066 | CTGGCCCCTTGCTCT[A/G]TTATGTTTTATTTCT | 11124 |
rs532496533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451659 | AACAGAGTGTATTAT[C/T]ACCTTAGGCATTTGG | 11124 |
rs532511483 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50767238 | AGCTCAAACACTGGT[C/T]CCCCAAAATAACTCA | 11124 |
rs532511577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50776594 | TCTGAAGTGATACAC[C/T]ATTCACTCACATGAA | 11124 |
rs532516803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955686 | ACATATATTTGAACA[A/C]CAATGTTTATGGCTG | 11124 |
rs532521365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50561628 | GTCAGGAGTTTTAGA[A/C]CAGCCTGGCCAATAT | 11124 |
rs532529204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932850 | ACATCTTCTGAAATC[A/G]AGGCAGAAGTTCTCA | 11124 |
rs532533395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50941555 | GTAGAGACAAGATCT[C/T]ACTATACTGCCCAGG | 11124 |
rs532548663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919742 | TCCACCAGCCTTGGC[C/T]TTTTACAGGCGTGAG | 11124 |
rs532548780 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950021 | AAATTTATTTTTTTT[G/T]GTAGAGACACGATCT | 11124 |
rs532549814 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50829172 | CTCTGCCAGTAGAGA[A/G]TAGGAGATAGGTTGT | 11124 |
rs532554127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662855 | GCAGGCACCCACTAG[C/T]GCGCCCGGCTAATTT | 11124 |
rs532561176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50577671 | CCTCATTAGACTGAG[A/C]AAAAGCAGGAAACCT | 11124 |
rs532572475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50767922 | AGGTAACAATCCGAT[G/T]ACTGGATCAAATCCA | 11124 |
rs532588059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618622 | GTGCTCCAATGCTGG[A/G]TGAGCATATATTTAG | 11124 |
rs532588511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824483 | GTTGACTGATTAATG[C/T]GAAAAAAAAAGGAAC | 11124 |
rs532590149 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50953779 | AAATTCATCAAGCAA[-/T]TTAGGCAGCAAAAAG | 11124 |
rs532603278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50587712 | ACTGTTAAGTGCTAC[A/G]CTGTTTGGACCTATG | 11124 |
rs532606679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50496410 | GCATTACTAAGCATG[A/T]CAGAAAGAAAGAAAT | 11124 |
rs532608628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770975 | CAACCATCTGATCTT[C/T]GACAAAGTTGACAAA | 11124 |
rs532610564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871291 | AGCTGTAGTAAGTTT[G/T]ATTCAGGACCTAGCT | 11124 |
rs532613575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50829088 | TCTAAGCTCAAAATA[A/G]TGGATTAAAAGCTAA | 11124 |
rs532615730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933528 | TCACTAATAGTATTT[C/T]TGTCAAAGCCATTCG | 11124 |
rs532620393 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50506026 | GGTCTCAGAGCAGCC[G/T]TTACATGTGCCAATA | 11124 |
rs532625223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50569839 | ACTAAGAAACCCAAC[A/G]TGCAGAGTTCTCTAT | 11124 |
rs532625277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50578494 | TAAATCCTGAAGTAC[A/G]GCAGTTAGCAATGAA | 11124 |
rs532631253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50641410 | ATTTAGTTTAAAATG[C/T]TACCAATCTTTTCTG | 11124 |
rs532632775 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50959525 | CCACACACATTGTAA[A/C]CCAAGTCATTAATAC | 11124 |
rs532634711 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FAF1 | GRCh38.p7 | 1:50698350 | CTCTGGCATTCAGGA[A/G]TCTAGGAGTTAATAT | 11124 |
rs532639279 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50729824 | TCAAGAGATTGAGAC[C/G]ATCCTGGCCAACATG | 11124 |
rs532656827 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50808511 | GCTGTCATCAAGAGA[C/G]CCATCACACATATAA | 11124 |
rs532679356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50926165 | AACATTACTGAAGCA[A/T]ATGATCACACTACTG | 11124 |
rs532696513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50846436 | TCCTGGGAACCAGCT[C/T]GCTTCCGAGCCGCAC | 11124 |
rs532697061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50655258 | AACTCCTGACCTCAG[A/G]TGATCCACACGCCTC | 11124 |
rs532698809 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | FAF1 | GRCh38.p7 | 1:50938587 | TTAGTTTAATCATGT[A/C]CCACTTGTCAATTTT | 11124 |
rs532709018 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50602653 | GACTACAGGTGCATG[C/T]CACCAAGTCCGGCTA | 11124 |
rs532709106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50586919 | TTTACAGTGCCTAGC[C/G]AGATTCACAGGCAAC | 11124 |
rs532710518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50687704 | CAGTGAGCCAAGATC[A/G]CACTCCAGCCTGGGC | 11124 |
rs532723480 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50806413 | ACTGTACAAACAACT[C/T]TCAAAACTGTGTGAT | 11124 |
rs532731312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50746710 | GAGAAATTCAAGCGG[A/G]CTGCAGAAGTTTACA | 11124 |
rs532733100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50738384 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCGT | 11124 |
rs532734912 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50826305 | CCTGTAATCCCAGCA[C/G]TTTTGGAGGCTGAAG | 11124 |
rs532738209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50640603 | TTTGGGCTTTTCTAG[G/T]TTTCTATTTCTCTTG | 11124 |
rs532744211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50929766 | TTCACAATTATTCAG[C/G]TAACAAAGTACATCT | 11124 |
rs532759932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674037 | CTCACTGCAACCTCC[A/G]CCAGCCAGGTGCAAG | 11124 |
rs532775921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565338 | TTTACAAATTTTCAT[A/G]ACAGTTGCTTAATTC | 11124 |
rs532788244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50455936 | AAATTAGCCGGGCAG[C/T]AGATGGCATGCACCT | 11124 |
rs532788463 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50883853 | AATTAGGCCAGGCGC[A/G]GTGGCTCATACCTAT | 11124 |
rs532789467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632437 | TCATGTGCAATCCAT[A/G]TGCTTGTTCATCAAT | 11124 |
rs532795318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50730514 | GTGCACTTACTCTGC[A/G]GTTATTATTCTATTT | 11124 |
rs532805870 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | FAF1 | GRCh38.p7 | 1:50840338 | CATACCAAAAATGTG[-/T]TTATTCTACAAATAC | 11124 |
rs532809168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886748 | ATTCAATGGTGTATA[C/T]GTGCCACATTTTCTT | 11124 |
rs532813278 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50912803 | AATCAATTGCTTACC[C/G]ATTCTCAGTTTCTTA | 11124 |
rs532821946 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50668699 | TCAAAAGCTCCATAC[A/G]ACTGGCCTTTAATTA | 11124 |
rs532827285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50633131 | ATGAGAAAATGGTAA[A/C]AGAACTGAAAGATAA | 11124 |
rs532833437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50513388 | ATCAATACTTGAGAG[A/G]CTAAGGCAGGAGAAT | 11124 |
rs532840802 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50614267 | GCACTTATTTACGTC[A/T]ATGCCACAAATCTGA | 11124 |
rs532846110 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50819703 | TATACATATATATAT[A/G]CATATATATATACGT | 11124 |
rs532853555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723227 | CCAACACGGCAAAAT[C/G]TCATCTCTACTACAA | 11124 |
rs532860640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50874953 | CTTTGTTTTTCGTTT[C/T]CTGTTTTTGTAGAGA | 11124 |
rs532867752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50678434 | AATTTACACATTTGG[C/T]CAGATTTTCTTCTCC | 11124 |
rs532869769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50500157 | TTTTTGGTTAGCTGA[C/T]TGTAAAATTCATGTG | 11124 |
rs532873273 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50867129 | TGGGATAACTGGTTA[C/G]CCACATGCAGAAGAA | 11124 |
rs532876685 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50598252 | AGTGAGCTGTGATCA[C/T]GCCACTGTACTCCAG | 11124 |
rs532876784 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50638070 | TTTTGGATAGAATTG[C/T]GAGTCATATAAGTTT | 11124 |
rs532879519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606780 | TGCTGGTATTACAGG[A/C]GTGAGCCACCGCGCC | 11124 |
rs532887734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50712427 | TTGGGAGGCAGAGGT[A/G]GGTGTATCCCTTGAG | 11124 |
rs532890854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922246 | GGCAGATCACCTGAG[G/T]TCAAGGAGTTCGAGA | 11124 |
rs532891878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50448533 | AACTTATTTGCCTGG[A/T]GAATTTGGGAGAAGG | 11124 |
rs532903379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775688 | AAAGGAAGAAAGAAA[C/T]GAACATATGGAAATC | 11124 |
rs532904714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50509841 | GGCAAGTTCCTTGAC[C/T]GCTTCCAACACTGAT | 11124 |
rs532913360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50686986 | GGCGCATGCCACCAC[A/G]CCCAGCTAATTTTTG | 11124 |
rs532913993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50517184 | AAACAAAATGCTAGA[A/G]TTCAAAATCATTTGC | 11124 |
rs532925380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50936630 | GTAAGCAATTTAATA[C/T]GAAATTCAAAGGAGG | 11124 |
rs532926041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874094 | CAATGACACTGATTT[A/C]CCTTTTTGGTTCTAG | 11124 |
rs532940951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50532297 | ATTAAAGGAATTAAA[A/G]TAAATTTCTTTACCA | 11124 |
rs532941385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50730056 | TGATAATTTGTTCCA[C/T]GAAAATTTATGAAAA | 11124 |
rs532946428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50674823 | AAAGATGAGAACAGC[C/T]ATTGCTAGAGCAATG | 11124 |
rs532950845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50590304 | TGTTTCCATTTATTT[A/G]TATCTTCTTTAATTT | 11124 |
rs532963388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581988 | TTCTTGTTATGGGCT[G/T]CTTCTTATAGACTTC | 11124 |
rs532963694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50564324 | ACTAGGTTAACCAGA[C/T]ATGGGACGAGGCAAG | 11124 |
rs532972229 | in-del | -/T | 0.266273 | 0.24947 | intron-variant | FAF1 | GRCh38.p7 | 1:50627834 | GTTTTCAACAAAACA[-/T]TTTTTTTTTTTAAAT | 11124 |
rs532981238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50473017 | AGAGCATCTGTTCTC[A/C]TTTGGACCAGCCTCT | 11124 |
rs532989096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50523114 | AATCCTTTATTAAGG[C/T]TAAATAATATTCCAT | 11124 |
rs532991496 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50939828 | TGGTGAATCACATTT[A/C]TTGAAGGTCATTTTG | 11124 |
rs532997391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50914841 | CTAGATCCAAACAAA[A/T]CACTATCAATATATG | 11124 |
rs533007463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50711628 | CATACCACCATGCCC[A/G]GCTAATTTTTGTATT | 11124 |
rs533009116 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50937312 | TGACAGACAAGCACA[A/T]CCAGAGGGGAGCTAA | 11124 |
rs533011408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725756 | CCACCACACCTGGCC[A/C]AAAAGCCATATATTT | 11124 |
rs533015191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760324 | ATTGAACTCAGCTCT[A/G]CACCAAGCAGACCTA | 11124 |
rs533017483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50573591 | ATCACAAAACTTAGC[C/T]CTGTTTAGCTCCTGA | 11124 |
rs533021762 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50842118 | AGACTCTGTTATACT[C/G]TAAGTATATTAAGAG | 11124 |
rs533024911 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50622220 | CCTGCCAGCTCACAT[C/G]TCCATGGAGGATAAA | 11124 |
rs533029158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510664 | TGGAATTCAGAAGAA[A/T]ATACTTAAACTGTAA | 11124 |
rs533047351 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50942354 | AAAAGTGTATATATA[C/T]GTACACATAAATTAG | 11124 |
rs533048806 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50734561 | AACATGGTGAAACCC[C/T]GTCTCTACTAAATAT | 11124 |
rs533049192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687606 | AATACAAAAATTAGC[A/C]AGGCATGGGGCGCGT | 11124 |
rs533054766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50480686 | GATGGACTGTATAAA[C/T]CATGGAGGTCTCGTA | 11124 |
rs533056212 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50738444 | TGAAACTCCGTCGCA[-/A]AAAAAAAAAAAAAAA | 11124 |
rs533072231 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50704345 | AGGAAAAAAAGGCAA[A/T]CTATATTTATTCATC | 11124 |
rs533078585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50628559 | CTTGGCTAACAGTTT[C/T]AGAGATGAAAAAGGC | 11124 |
rs533084103 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50909422 | TTTGAATGTTGGCCT[C/G]CCTTGCTAGGTTGGG | 11124 |
rs533097602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582507 | GTGAAGAGTTCCATG[C/T]TTTTGGAAAAAAACA | 11124 |
rs533098259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667187 | AAATCAAGGAAAAAG[A/G]AGAAGAGCATATAAA | 11124 |
rs533098274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50658966 | GCAAAAGCATCAAAA[C/G]AGTGGGGATTTTACT | 11124 |
rs533104434 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50675182 | GGCGTGAGCCACAGC[A/G]CCCAGCCAGACCTTG | 11124 |
rs533106667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681461 | TTGGAGCTCTTATTT[C/T]TAAATATCTTCAATA | 11124 |
rs533119205 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50579820 | ATATCTAATACTCAA[A/G]TATAACTTGTGATCC | 11124 |
rs533124436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50786696 | CATAGAAGAAGAAAC[A/G]AGTATAAAGGCCCAG | 11124 |
rs533127775 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | FAF1 | GRCh38.p7 | 1:50809316 | TAAAAGATCAATAAG[A/G]TCAAGAGTTAGTTCC | 11124 |
rs533129598 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | FAF1 | GRCh38.p7 | 1:50518390 | TTGTTTTTAGTTTTG[G/T]CAATTATGAACACAG | 11124 |
rs533130185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50741999 | GCAGAAATCACCTAG[A/T]GAAGAGTACATAGAA | 11124 |
rs533131016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722375 | ACTATAAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 11124 |
rs533131070 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50519347 | AAAGAAAGGAAGGAA[G/T]GAAGGAAGGAAGGAA | 11124 |
rs533131545 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590421 | GACATTGGAATTGTT[G/T]TTCTAATTTTCTGTT | 11124 |
rs533133601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525315 | ATTGATTCTTCTTAC[A/C]TTTGAGCATGAAATG | 11124 |
rs533135792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744193 | AATTCATTCCATGCA[C/T]CTGCCACTATCCAAG | 11124 |
rs533148420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50643749 | AAGCATGCACCACCA[C/T]GCCTGGCTAATTTTT | 11124 |
rs533153316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50638082 | TTGCGAGTCATATAA[C/G]TTTTCTAAAACCCAT | 11124 |
rs533168913 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50477031 | TTTGACCTATGCAAA[G/T]TATCTGTTAAAAAAT | 11124 |
rs533171553 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FAF1 | GRCh38.p7 | 1:50889614 | TTTCTGCCTTCATTT[C/T]GTTATGTACCCAGTA | 11124 |
rs533172816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467071 | CATGAACTGCAGTAT[A/G]AGGACTGTTTGTATG | 11124 |
rs533175411 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50894317 | ATTAAAAAAAAAAAA[A/C]AAAAAAAAAAAAACT | 11124 |
rs533177565 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | FAF1 | GRCh38.p7 | 1:50888264 | TTGCTTATCACCTTA[A/C]GGAGATTTTGGGCTG | 11124 |
rs533187476 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50486015 | GGGATTACAATTTGA[G/T]ATTAGATTTGGGTGG | 11124 |
rs533190398 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794157 | CCACAAAAATACAAG[A/G]GCTGCCACCTTGGTA | 11124 |
rs533190537 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50613329 | TCACAAAGACTTAAA[A/G]CTACCAATCAAAATA | 11124 |
rs533195577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50733942 | GCTCGGGTTACAGGC[A/G]TGCACCACCACACCC | 11124 |
rs533198549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50483209 | GTTTTCTATGGGATT[G/T]TTTTTGGATATAAAT | 11124 |
rs533207923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50797268 | TATTGAATCAAAAAA[C/G]AGTAAATGTATTTTT | 11124 |
rs533211920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50473974 | TAAGCAAGTCCAAGT[A/C]CCATTCCATATAAAG | 11124 |
rs533214606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888664 | TATATGCTGGATTAC[A/G]TTTACTGATTTGCGT | 11124 |
rs533215354 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50552681 | TTCTGAAGGAATATA[C/T]AGACAGGATAGAAAA | 11124 |
rs533227450 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50924433 | GAACACAAACAAAGG[C/T]ATCCCATACTCATTG | 11124 |
rs533227533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50630253 | AAATACTCCATGTTT[A/G]GTTGTAAGACATATT | 11124 |
rs533235034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518621 | AATTTTTTGTATTTT[C/T]AGTAGAGACGGAGTT | 11124 |
rs533243915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50680558 | TGTGGTGGTGGGTGT[C/T]TGTAATCCCAGCTAC | 11124 |
rs533254765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50780530 | TGGGTACGGAAACCA[A/G]TGATCTTTGACTTTC | 11124 |
rs533256360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931650 | AGGCGGGTGGATCAC[A/G]AGATCAGCAGGTTGA | 11124 |
rs533257473 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50523817 | TTTAGGTTGATTCCA[C/T]GTCTTTGCTATTGTG | 11124 |
rs533259476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50475221 | CTGGAATAGGGAAAA[C/T]AGCTAGGAAGGAAGA | 11124 |
rs533261126 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50553642 | CACTATGCTTGATCC[C/T]GGCACCTTTAGAAGG | 11124 |
rs533262604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50631359 | GTCCCCATCAGGACA[C/T]AAATCATCCCTTTGT | 11124 |
rs533265272 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50451194 | TAAGGTGGGAAAGAG[A/G]GAATGAAAGAAAAAT | 11124 |
rs533267325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620954 | TGTTAGGTGTTCCGG[A/G]CCATGGGGCCCCCTC | 11124 |
rs533283404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50673183 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 11124 |
rs533287522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50533278 | GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTCTT | 11124 |
rs533292391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50675951 | CACATCAATTCTATG[A/G]GTATAGAAATTGCTT | 11124 |
rs533298378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50882878 | GTAATCCCAGACACT[C/T]GGGAGGCTGAGGCAG | 11124 |
rs533298653 | in-del | -/CTCT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50836109 | GGATGTACATAAATA[-/CTCT]CTCTCTCTGTATGTA | 11124 |
rs533298764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772291 | GAAAGCAGTTTGGCA[A/G]TCTCTCAAAGAACTT | 11124 |
rs533304975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607373 | TTATCACCTGTATGA[C/T]GAAAAAATTGGACTA | 11124 |
rs533309897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778969 | TTCTTTTACAGTTGG[A/G]GTCAATTCTCTCAAA | 11124 |
rs533311335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682087 | CAATCCACCCACTTT[A/G]GCCTCCCAAAGTGAA | 11124 |
rs533328289 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50938924 | TGTTCCATTGGTCTA[C/T]GTGTCTGTTTTTGTA | 11124 |
rs533348918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50858418 | AAAATCGAAAACTAT[A/G]AAACTAGATCTGTGC | 11124 |
rs533353007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50750692 | GCAGTGGCGCAATCT[C/T]GGCCCACTGTAACCT | 11124 |
rs533360436 | snp | C/T | 0.000292702 | 0.012094 | synonymous-codon | FAF1 | GRCh38.p7 | 1:50475668 | GGCTTGCTCTAAGGA[C/T]AGCCGGATGGCCTAG | 11124 |
rs533365428 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50449420 | ATTATAGTGAAGCTG[A/T]CTATATTTGCTTTTG | 11124 |
rs533376206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50651788 | AGCAGATGCCTCCAC[C/T]TGAATGATTTCAGTA | 11124 |
rs533383948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50657723 | ACATCTAAGTTACCA[C/T]TCCAGTGAAATAGAG | 11124 |
rs533389484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939768 | AAAGCTTTTTCTGCA[C/T]CTATTGAGATGATCA | 11124 |
rs533395343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50492021 | TAACTCTACAAACTG[C/T]GTGACCTTGTATAAG | 11124 |
rs533397872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705221 | CTCTCTTGGGGGAGG[C/T]TCTCTTTTGAAACAG | 11124 |
rs533400330 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50952681 | CATCTCTGCCCGGCC[A/G]CCCATCGTCTGAGAT | 11124 |
rs533411589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836085 | TCATCTATTTCACAA[A/T]ACAGAAATAGGATGT | 11124 |
rs533411736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645461 | TCAGGTTTTGTGGGC[C/G]ACATGGTCTTTGTTT | 11124 |
rs533418950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736871 | AGGTTCTGCATGGAT[A/T]TTGTTTTGTTTTTTA | 11124 |
rs533432613 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50771088 | CTTCCTTACAGCATA[A/T]ACAAAAATCAACTTA | 11124 |
rs533453640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923793 | AAATCAATAAATACA[A/G]TACATCAAAATAACA | 11124 |
rs533456230 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874115 | TTGGTTCTAGTACCT[C/G]ACAATTGTCTATTTT | 11124 |
rs533465131 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687931 | ACAAGGTCAGGAGTT[C/T]GAGACCATCTTGGCT | 11124 |
rs533477693 | snp | C/T | | | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471221 | CAAACTTCATCTAGA[C/T]GTAGCTTCTGGATTC | 11124 |
rs533479529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850676 | AAAATGAGTACCTGG[A/C]AGGTATAAGTAGGAA | 11124 |
rs533486424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526095 | ATTGATATCGTTTGC[A/G]ATATTTCACAAAGGT | 11124 |
rs533487398 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FAF1 | GRCh38.p7 | 1:50591675 | GAGACTCCATCTCAG[A/G]AAAAAAAAAAAAAAA | 11124 |
rs533491123 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50683155 | ATGGTTAGAAAAACA[G/T]TATTTTAAAAAAAAA | 11124 |
rs533502254 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50520548 | CTTTCCAGAACCAGA[G/T]CAAATCTTACCTCTT | 11124 |
rs533513713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876064 | TATAGTAGGATATGT[A/G]CTATAATAGTATGTA | 11124 |
rs533514488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50783791 | GAGGCATGAGAATCA[C/G]TTGAACCTAGGAGGC | 11124 |
rs533514807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775234 | GAATTAATATATACA[A/C]ATATATTCATATACT | 11124 |
rs533517842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50781302 | TAAAATCACTTCAAA[A/G]AGAAAAAAAAAAAGA | 11124 |
rs533521926 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | FAF1 | GRCh38.p7 | 1:50441426 | GAATGGCTGGTTCCA[C/G]CGCTGGGCCGTGTTT | 11124 |
rs533523602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598708 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCTCAGC | 11124 |
rs533530220 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50908778 | TGTGTCTCTGCACAT[C/G]AGATGGGTTTCCTGA | 11124 |
rs533533843 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50933777 | TTTAATTCGATTTAC[A/G]GTTCCACATGGCTGG | 11124 |
rs533541212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659499 | TGTGTTGCTTCTGAC[A/G]GAGTTTCATCTTTAG | 11124 |
rs533552006 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50491254 | ATTTAGGATTCTTGG[C/G]TTATGTTACAGCTAC | 11124 |
rs533572796 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50504032 | CATAGGTGTGGTTTA[C/T]TGTATATCAATTGTA | 11124 |
rs533575996 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739572 | TACTTTTTCACTGAA[A/G]AAGTATATCCTTGCA | 11124 |
rs533576486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50903789 | CTCCCTTAACAAGAA[A/G]TTAGGGAAGAGTCTC | 11124 |
rs533578749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50548968 | TGGATTAATAAATTC[C/T]ACTTGTTTTTCTTTC | 11124 |
rs533595025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822604 | CTCTTCCTTCTGCTC[A/C]CTGTATAACTGCCTT | 11124 |
rs533606276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50945426 | TGCCACTGGCTTCTC[C/T]CATCATGTGACAAAC | 11124 |
rs533617223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625416 | GAGGGGTTCACAAAC[A/G]GTAGTGAATAAACTT | 11124 |
rs533619639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50500752 | TGTACCCCATAAATA[C/T]GTACAACTATTATGT | 11124 |
rs533625005 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50775952 | TCTGCCTGCCATAAT[A/G]CTCATAAGGCAATAA | 11124 |
rs533625488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50715307 | ATTTTAAAATTGAAG[A/G]TGGCGGGGTGGGAGC | 11124 |
rs533632634 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50837116 | GCACCCGCCACCATG[C/T]CCAGCTAATTTTTTG | 11124 |
rs533634572 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50766047 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 11124 |
rs533635101 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50766738 | CACCTTATACCACAA[A/T]CAAACCCCCAAGGGC | 11124 |
rs533644976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50514437 | GATTATGGCAAATCT[A/G]ACATGACACTCTTTC | 11124 |
rs533662541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50796356 | CTAGCTTTTTTTTTA[C/T]GGCACCTTTTCCATA | 11124 |
rs533664116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543152 | CTAATAAATCAGATA[C/T]GGCAAAAAGTAATCT | 11124 |
rs533667940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895474 | AATACCAATCCCACT[C/G]GAACTATTACAAAAA | 11124 |
rs533675885 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50841250 | CACATATATATAAAA[C/T]TTTGTCTTCAACATT | 11124 |
rs533677041 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50726297 | GAACCGTAAGTCCAG[C/G]ACAAAAAGATAAAAG | 11124 |
rs533688930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50788587 | TAACTCTGCTTTCCA[C/T]GGATTATTTTGAAAC | 11124 |
rs533692874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695850 | GACAGGGTTTTGCCA[C/T]GTTGGCCAGGCTGGT | 11124 |
rs533697987 | in-del | -/TAGC | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50635732 | TGTATAGATGCCATT[-/TAGC]TAGCTCACTCATCTG | 11124 |
rs533700745 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50542232 | TTGAGATTTTCAAAT[G/T]GCAATCATCAAGAGC | 11124 |
rs533703004 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50673187 | TGCTTGAACCCGGGA[A/G]GCAGAGGTTGCAGTG | 11124 |
rs533707590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897120 | ATATGTGCAAAATCT[A/G]TATGAGGAAAACTAT | 11124 |
rs533715317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50647112 | CCTCAGCCTCCCAAA[A/C]CGCTGGGAGTATAGG | 11124 |
rs533718658 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50868354 | AGATAAAATAAAAAA[-/T]GTAAAAAAGAAAGTA | 11124 |
rs533724170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50838260 | AAATGAAGAATCTAT[A/G]CTTGAGGATATTCAT | 11124 |
rs533724302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50829604 | TCAGGATTAAAGGCA[A/G]TCAAAGGTAACACCC | 11124 |
rs533741016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50745384 | TGTATTAAAGAGAAG[A/G]GCAACAAGAATTTCA | 11124 |
rs533743517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897716 | CATGCATCCATACCA[C/T]TCAACTCTATAGTCC | 11124 |
rs533745082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845573 | GTACCCACTCTTCTG[C/T]TTGCTGATTTGCTCC | 11124 |
rs533751120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50647760 | TTGTTCGACAGTTAC[A/G]GAGACTGAGATCCAT | 11124 |
rs533763231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50640069 | CTGTGAAATTCAATT[C/T]GGTAAAATGTGTTAA | 11124 |
rs533766963 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50653919 | GTAATCCACCGGCTT[C/T]GGCCTCCCAAAGTGC | 11124 |
rs533768128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50461075 | TTTCCCCTAGGAACA[G/T]TGGTTGAGTATCCAC | 11124 |
rs533780333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50722638 | TGGGCGACAGAGAGC[A/G]ACAGTCTCAAAAAAA | 11124 |
rs533781624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570208 | CAAAGCCTAGGAAGA[C/T]TAAACATCCATGCTG | 11124 |
rs533798311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886889 | AATCCTCTGGGTATA[C/T]ACCCAGTAGTGGGAT | 11124 |
rs533799233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50640903 | CAGTGGCACCATCTC[A/G]GCTCACTGCAACCTC | 11124 |
rs533801359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694545 | TCTCTTCTATAACAC[C/T]ATAGCCAGGAAAAAA | 11124 |
rs533806620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50631992 | ACTTTACTACAGATG[A/T]ACATGTATATGAAAA | 11124 |
rs533809531 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50730391 | CTAGTATTTTGTTTA[C/T]GCTTACTCTCATTTT | 11124 |
rs533809818 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50561146 | TTTGGGAGGCCAATT[A/T]CTTCTGGGGTATCAC | 11124 |
rs533811327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50926536 | GTGACATGGTTAACT[A/G]TAATTTATTGTATAT | 11124 |
rs533811389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50624938 | AGCAGTTTTGCTCTT[A/G]TTGCCCAGGCTGGAG | 11124 |
rs533813934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50830481 | TTTCTATGATAGTTA[C/T]TAGAGTTAATTCAAA | 11124 |
rs533824244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906621 | GTTGGATTCCTAGGT[A/G]TTTTGTTCTCTTTGA | 11124 |
rs533827073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50890956 | ATCCTGCAGAGTGTT[C/T]TCCAACTTGGTTCCA | 11124 |
rs533830715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50519776 | TCAATTGGAAAAGTA[A/C]CCTTCTTTCTTCTAG | 11124 |
rs533830922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528148 | GCTGAGATTATAGCC[A/G]TGAGCCACTGCACCC | 11124 |
rs533831416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452709 | CTTAAAAGCCTTCTG[A/T]GAGATCCTGATTATT | 11124 |
rs533834511 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50477645 | GTAACCCAGTGAATG[A/G]ATTAACATCTGTGTA | 11124 |
rs533837502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618349 | TTTTCGCTAATACTG[C/G]TGTTCACTCAGGAGT | 11124 |
rs533844444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659966 | CCTGTTTATATACTA[C/T]AATTAATGTGAAAAA | 11124 |
rs533846855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50782984 | CAACAATACTGAGTG[C/T]TTTTTTTAAAGATCA | 11124 |
rs533862954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50891375 | TTCAAAGTCATTCTC[C/T]ATCCAGCTTTGTTCC | 11124 |
rs533877711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610368 | GATTTCACACCATAA[C/T]GGCTTACCACAAAAA | 11124 |
rs533893093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50595645 | CCTGCTGGATTCAAG[C/T]AATTCTCATGCCTCA | 11124 |
rs533896546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50458889 | GGCTAAGTAATTTAC[A/G]CAAGATCAAACACCT | 11124 |
rs533898206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50596060 | ATAAAAAAAAAGGGA[A/G]GTGCGCAGGTAGGTG | 11124 |
rs533908267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50942846 | TACATCATGGATTGC[A/G]TTACGGGAGAGGAAC | 11124 |
rs533918717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649246 | CAACCTCCGCCTTCC[A/G]GGTTCAAGCAATTCT | 11124 |
rs533922523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870900 | CTTAATGAGAAAGAA[A/G]TGTTGAAAGTTGAGA | 11124 |
rs533934034 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50767508 | ATGCCCAAGACACAT[A/T]GTCTTCAGATTCTTA | 11124 |
rs533954753 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907769 | TTTGATTCTTCTCTC[G/T]TTTCTTCTTTATTAG | 11124 |
rs533956769 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729030 | TATCTATCTATCTAT[A/C]TATCTATATATATAT | 11124 |
rs533960982 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50535994 | CTGAAACCAGAAGAG[C/G/T]CTGACTCGAAGCCTG | 11124 |
rs533965272 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50839540 | AAAGGGCCTAAATAC[G/T]GTTGATCAGATTTTG | 11124 |
rs533969283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943624 | AATTGAATGACTCCC[A/C]TTATAAAGATAATTC | 11124 |
rs533994696 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881210 | CCCATTCCCAGAGAC[C/T]CTTTTTTGGTTAGTT | 11124 |
rs533997739 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50758097 | TAATTTTTGTATTTT[C/T]AGTAGAGACGATGTT | 11124 |
rs534000061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50580185 | GTTTTAATTATTTAT[A/T]TTTATTTTATACTTG | 11124 |
rs534003532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50741184 | ACAGAAGCCTGTTGG[A/G]GAAGGTAACCTTAAG | 11124 |
rs534008105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685625 | TCCTCAGCAGGACCA[C/T]TGTGTTGCACAGCCA | 11124 |
rs534008914 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50647987 | GTCTTGGCTGGGCGC[A/G]GTGGCTCACGCCTCC | 11124 |
rs534018137 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50633085 | AAGCTACTTGCCTCT[A/G]AACAACAAAATGTTG | 11124 |
rs534018315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50690234 | CAGGTGATCCACCCA[C/T]CTCAGCCTCCCAAAG | 11124 |
rs534019664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50588734 | CAGAGGCTGCAAGGG[A/C]TACTGGAGTCCTCTG | 11124 |
rs534024263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50798957 | CAATCTTGGCTCACT[A/G]CAACCTTGGCCTCCC | 11124 |
rs534029262 | in-del | -/ATATATATATATATATATATATTTTT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746272 | TATATATATATATAT[-/ATATATATATATATATATATATTTTT]TTTTTTTTTTTTTTT | 11124 |
rs534046576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50831856 | AAGGCCCTGTGAAGG[A/G]TGGTAATGTGAGCCA | 11124 |
rs534057341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50690744 | AAAATTCAAACCCAA[C/T]AGCAACCATTAACTA | 11124 |
rs534060810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50738738 | TGATATACTTCATAG[C/T]AGTTGGTAAGGTCAA | 11124 |
rs534061274 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940302 | TCTATCCAGTCAGCA[A/C/T]TGGCAGAGTATTTTT | 11124 |
rs534068824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468750 | AGGTGTGAGCCACCA[C/G]GCCCGGCCTAATTTT | 11124 |
rs534071499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50586156 | TTAAAAATCTGTCAT[C/T]GGCGGTTTTCTAACT | 11124 |
rs534078992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919835 | TTAAGAGGAACTGTG[A/G]TAAGTAAACCATGTA | 11124 |
rs534084919 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50948425 | GTGTAAGGCAAAGCG[C/G]GAGACAGCCTCTCAC | 11124 |
rs534087618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50791593 | TTTTCAGCATTCTTA[C/T]AACCAGCTTCTTGAT | 11124 |
rs534100372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50837799 | CCCAGGCTGGAGTGC[A/G]GTGGCGTGACCTCAG | 11124 |
rs534107853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684593 | AGTGTTTTTAAGAGT[C/T]TGCCAATCTCCATGA | 11124 |
rs534109042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50587218 | ACCTTACTTCATACT[A/G]AGATAGTGATTTTAA | 11124 |
rs534113246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50553166 | AGATTGGAAGGCATG[A/T]GGAGATAAAAAAATC | 11124 |
rs534143012 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530541 | TGGGTACAAAAAGAA[G/T]AGAAAGAATGAATAA | 11124 |
rs534145116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50924990 | CTCCATCTCAAAAAA[C/T]ATAACAAAACAAAAC | 11124 |
rs534152974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50561695 | GCCAGGCGTGGTGGC[A/G]CACACCTGTAGTTCC | 11124 |
rs534160991 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50550224 | GGCATGGTGGCAGGC[A/T]CCTGTAGTCCCAGCT | 11124 |
rs534161254 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590791 | GTTTGAGACCAGTCT[C/G]ACCAATATGGTGAAA | 11124 |
rs534163004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912180 | AAGGGCTTGAGCTGC[C/T]GCTAGACAAGTCACT | 11124 |
rs534164799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50899730 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 11124 |
rs534168620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50529512 | GTGAACAAAAATCAA[C/T]CTGTTGCTTATTCAT | 11124 |
rs534169662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906218 | ATTTCTGAGGGCTCT[G/T]TTGTATTCCATTGGT | 11124 |
rs534173565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816322 | CCATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT | 11124 |
rs534176140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50747659 | TGATTGTATTTTGCA[A/G]TGTGAGAAGGACATG | 11124 |
rs534184851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50700711 | AGCTATCATGTTTGA[C/T]ACACATATCTTAAGT | 11124 |
rs534187812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709684 | ACCTGAGCATCCTAT[C/T]TCCCAAAAGGCTAGG | 11124 |
rs534194146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847252 | TGGCTTTGATAATAA[A/G]CGTGATTTTAGAAAT | 11124 |
rs534199224 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50642662 | TAAAAAATAATAATA[A/C]TAAAATAAAATAAAA | 11124 |
rs534202804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50740251 | TGTGGGGTTGAGCTT[A/T]GCAATTTTAAACAGG | 11124 |
rs534205046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50538022 | ATCTATACATGATTT[G/T]ATAACATACATTGGT | 11124 |
rs534222912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50691665 | GGCGCGATCTCGGCT[C/T]ACGCAACCTCCACCT | 11124 |
rs534228632 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50937211 | AATACAATGTGCACA[A/G]CTAGGTGAAAGTCCA | 11124 |
rs534237472 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50837203 | CCTCGTGATCTGCCC[A/G]TCTTGGCCTCCCAAA | 11124 |
rs534246385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479980 | TGTAAGCAAACACTG[C/T]TGTAAAACAACAACA | 11124 |
rs534248084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50701332 | GCACATTCTCAGTTA[C/G]CCTACTCTTACTTCA | 11124 |
rs534261261 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50794539 | CTGAAAAGAATAAAA[C/T]TGGAAAACTGGGTGA | 11124 |
rs534261508 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50873528 | AAGACAAACTTAAGA[-/AT]AAATGGCCAGAACCT | 11124 |
rs534265393 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50732134 | GGCTGGAGTGCAATA[C/G]CCCGATCTCAGCTCA | 11124 |
rs534272372 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50947851 | GATAGATATCAAAAA[G/T]ACATAAACATTTACA | 11124 |
rs534283437 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50522044 | AAATGTAAACAGGGA[A/C/T]GGTATGGATATATCT | 11124 |
rs534286492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50903973 | TGGCAGCCCTCAAAA[A/C]ATTAAATTTAGAATT | 11124 |
rs534294660 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50902984 | GGTGTTATTTCTGGT[A/C]ATCTTGGTCCTTCTC | 11124 |
rs534299387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50785274 | AATGAAAGAAAAAAT[A/G]GACAAGTGGGACTTT | 11124 |
rs534303452 | in-del | -/TGATA | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50554687 | GCTTATGTTATAATC[-/TGATA]TATCAAACCTCACCA | 11124 |
rs534310336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470916 | TTCCTTTATAATACT[A/T]TCCGTTATCACAGCC | 11124 |
rs534313394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50850113 | TGGATAGTTCCTGAA[G/T]GGTTAGGAGCTACGA | 11124 |
rs534314222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50679320 | TTAAAAAAAAAAAAA[C/G]TACAAAAAAAAAGAA | 11124 |
rs534318690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50887929 | GAAAGTCATTGGTAG[C/T]TTGATGGGGATGGCA | 11124 |
rs534332545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50549522 | TGGTGGCTCACGACT[A/G]TACTCCCAGCACTTT | 11124 |
rs534344480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50843759 | TGTGTGTGTGTATTG[C/T]ATTTTCTTTAATTCA | 11124 |
rs534347744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50495778 | CCAGCATTTGTTATT[A/C]CCTGTCTTTGGGATA | 11124 |
rs534350937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50761243 | GATGAATTCACAGCC[A/G]AATTCTACCAGAGGT | 11124 |
rs534352256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50620911 | GGGTGCCCCCTCCAG[G/T]CACTGGCACTGTGCC | 11124 |
rs534364969 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50937932 | TGTATTCCTTACATC[C/T]TTGCATCACAAGACA | 11124 |
rs534370948 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50484914 | GAACAATGAGAACAC[C/T]TGGACACAGGAAGGG | 11124 |
rs534380025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862796 | TAAAAAAGACAAAAA[A/G]GGACATTATATAATG | 11124 |
rs534384846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815688 | TAAGTGTTTCCTTTT[C/G]CCTATAGCTTCATCA | 11124 |
rs534393060 | in-del | -/AC | 0.0146544 | 0.0843353 | intron-variant | FAF1 | GRCh38.p7 | 1:50740836 | TAACATGCAAACAAC[-/AC]ACACACACACACACA | 11124 |
rs534401427 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | FAF1 | GRCh38.p7 | 1:50532786 | TTGGGTTTCATTTTT[A/T]AAAAATATTTTAAAA | 11124 |
rs534403337 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927983 | ATACTGTTAGGATTT[A/G]TGTTCTTTGCTGAGT | 11124 |
rs534403609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591849 | TACATCAAATCATGC[C/T]TTTTTTCTCTGAATG | 11124 |
rs534409176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50444813 | GGTTATCTTGCCCAA[C/G]GCTGCAGACAGAATA | 11124 |
rs534410033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753613 | TCATCTGGTGGCTTT[C/T]CACTTCAGACATCAC | 11124 |
rs534414204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453355 | GTGCATTGCTCTGCA[C/T]GCAAACACCACTCAA | 11124 |
rs534416111 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830129 | TTTGGGTCTTTTTGG[C/T]TTTTTTGAGACAGAG | 11124 |
rs534428653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50835520 | GGGTTGCAGTGAGCC[A/G]ACATTGCGCCACTGC | 11124 |
rs534428747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844489 | ATCAATGGCCTTTGC[A/G]CACAGCAAAATATAA | 11124 |
rs534435549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50611262 | GCTTTGTATTAGGGA[G/T]AAAGAATTTTCTTCT | 11124 |
rs534436651 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50682302 | CCCAGGAGTTCCAGA[A/C]AAGCCTGAGCAACAC | 11124 |
rs534454419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708941 | TGCAGTGAAGGCTGC[A/G]TGAGAGAAGTCTACT | 11124 |
rs534456148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955859 | GACTCTTGGGCACAT[A/T]ATGCTAAGTGAAATA | 11124 |
rs534481620 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50504100 | CAAAAAATTAATAGA[C/T]GGATGACACAGTAGC | 11124 |
rs534486811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906549 | TTGTATCCTCTTTTA[C/G]TTCATTGAGCAGTGG | 11124 |
rs534494182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50819379 | CAGCACTTTGGGAGA[C/T]TGAGGAAGGGAGATC | 11124 |
rs534494445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50557068 | GCTCATTTATTACTG[A/G]GACTAGGCTATGTAA | 11124 |
rs534519347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659108 | TTCTGAAAAAAGTTA[C/G]TATTCTAGGAAACCT | 11124 |
rs534523269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447976 | ACTTTTCTTGTCTAG[A/G]CTTTAATTTTTGCAT | 11124 |
rs534525104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50595354 | TCACTGTACCTGGCC[A/C]CTGTTATTTTATCTA | 11124 |
rs534526245 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50746964 | CCGCTGCTTCCATGT[C/G]GTGTTAAGCCTGCAG | 11124 |
rs534532027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50555995 | TATGGTGTGTATATA[C/T]ATGGTGTGTGTATAT | 11124 |
rs534538342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705975 | GCAAAAACCCCAGGA[A/G]TACCCTAACCTCCAC | 11124 |
rs534554713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50755970 | TTCTTTCTAGGCCTC[C/T]GGGTCTGTCATGGGA | 11124 |
rs534556985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50750963 | CAAACAAATAGCTCC[A/C]AGTTTAGCTCTTTTT | 11124 |
rs534559968 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50585894 | TAAAAAAAAAAAAAA[-/G]AAAAAAAGAAAAAAG | 11124 |
rs534563175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50712087 | GAGATAACACTCTTA[C/T]GATTGGACCTTCAGG | 11124 |
rs534565561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50704833 | ATTCAGAAGCTGAAA[C/T]TCATTAACACAATAT | 11124 |
rs534582540 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50931542 | ATCCCTGATAAACCT[A/G]TCAGATCTCAAGAGA | 11124 |
rs534587313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645083 | TGTTTAGTCTTTGCC[C/T]GTGTTATTTGCAAAA | 11124 |
rs534588749 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50759147 | TCTCTTTTATTTTAA[-/T]TTTTTTAAAATTATT | 11124 |
rs534590430 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50541462 | GCTTAACTCATCGAT[A/G]GGGATGTATAGATCG | 11124 |
rs534594462 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606855 | TCATTACCTGCTTAC[A/C/G]ACTGGGAATTTCGAA | 11124 |
rs534612352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904700 | GTAGAAATCTTCCTG[C/T]TTATAAATATTACTA | 11124 |
rs534625575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705358 | AGGGCAGGATGGAGC[C/T]GCTTAAGAAAAGTCC | 11124 |
rs534627985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645626 | TCAGGAGTTTGAGAC[A/C]AGCCTGGCCAACATG | 11124 |
rs534636066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50804920 | AGGGCTCAGGAGAGG[C/G]GCTCAGATGGAGGGG | 11124 |
rs534637030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952551 | TGGGAAGTGAGGAGC[A/G]TCTCTGCCTGGCCAC | 11124 |
rs534640923 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50570529 | CAGGAAAACACACTT[-/A]AAAAAAAAATTCCCA | 11124 |
rs534643653 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50655919 | ATATTTCAAGTTTCT[A/G]TGTGGAATAGTGAAG | 11124 |
rs534649949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50651260 | GTGAAAAAGTATTTT[A/C]ATCTAGTTAATTAAC | 11124 |
rs534654413 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50492870 | AATTCCTAAAAGCTC[G/T]GGTATGAATAGGAAC | 11124 |
rs534655068 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50667765 | TTTCCTTTTCTTCAA[-/G]GAAAAAAGATTTTTT | 11124 |
rs534675063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50660772 | GCTGGAATTACAGGC[A/G]AGCTACCTTACCCAG | 11124 |
rs534677931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938530 | ATTCTGTAGGTTGTC[G/T]GTTTACACTGTTGAT | 11124 |
rs534680040 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960836 | AGAAGAGGAGGAGCA[-/T]TTTTTTTTAATTGAT | 11124 |
rs534694245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896216 | CCTGAGCCCGGGAGG[C/T]TGAGGCTGCGGTGAG | 11124 |
rs534696560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50713742 | AGTTGAGATTACAAC[C/T]GTAAGTCACTGCGCC | 11124 |
rs534702653 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50788944 | TCCAGCAATCAATCC[A/C]CCCCAGCCTCCCAAG | 11124 |
rs534712710 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50685935 | TAGAAATATAAATGA[C/T]ACATGATAATTTCCC | 11124 |
rs534726738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50789862 | CTCTATGCTAACAGG[C/T]GCATGGTCTTTCATT | 11124 |
rs534726924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50485657 | CCTGGGCAACAGAGC[A/G]AGACTGTCTCAAAAA | 11124 |
rs534732610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689189 | CTAAATTTTGTTATG[C/T]ATATTTTACAATTAG | 11124 |
rs534738847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608650 | CCTACCCCAAAATGT[A/C]TCCCCCTATCTCTCA | 11124 |
rs534747939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910151 | GCTGGAGGTCCACTC[C/T]AGACCCTGTTTGCCT | 11124 |
rs534752999 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50785738 | AACAGTATGGAAGTT[C/T]CTCAAAAAATTATAA | 11124 |
rs534755510 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50522920 | TAACTTCCCAATTTA[C/T]CCTACATCTTTAGTT | 11124 |
rs534756463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50706523 | AACCATGAAGAGTAT[C/T]TGAAATTAGTGAAAA | 11124 |
rs534757685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534410 | CTCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAA | 11124 |
rs534774631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609139 | TAGAGATAGAGCCAA[C/T]GGTGAACAGTTTCTG | 11124 |
rs534775230 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50510099 | TGAACCTGGGAGGCG[A/G]GGGTTGCAGTGAGCC | 11124 |
rs534776781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486555 | TCTACGGGCGCACCG[C/T]GAAGTCTTTCTTGTT | 11124 |
rs534781241 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50545601 | AAAAAAAGAAAAAAG[A/G]AAAAAAAAACATTTT | 11124 |
rs534785172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875110 | AATACTGAATTTTTT[A/T]GTTTTTCAAAGTATT | 11124 |
rs534787707 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905256 | ATCCCATGGTGTACA[A/T]GTGCCACATTTTCTT | 11124 |
rs534792027 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50854592 | CCTGCAGTTACCCCA[A/C]AATAAGTGGAGCCAA | 11124 |
rs534806739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50958956 | GATATTAGTTCTAGC[C/T]CCAAGTCTTTCACAA | 11124 |
rs534810116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50448735 | ATCTCTGATCAACTT[C/T]TCCGGTAACAAAGGA | 11124 |
rs534818195 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50507367 | TTCTAAGTTAGTACC[C/T]GGCTGGTGTGAGAAC | 11124 |
rs534818980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851944 | TCATAACTATTTAAT[C/T]ATAGTTTAGCAGTGT | 11124 |
rs534820061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50819925 | ATATAAATAAATATT[G/T]TTCCACTTTAATTGA | 11124 |
rs534821681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50752055 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 11124 |
rs534828359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50503391 | TTTGGGAGGCAAAGG[C/T]AGAATTGCTTGAGGC | 11124 |
rs534831964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456905 | CTTGTCTCAAACTTC[C/G]TGTGTACAATTTTTT | 11124 |
rs534851063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543729 | ATACATTAGCAAAGA[C/T]TTGTTGACTAAACCA | 11124 |
rs534854294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585146 | TGGAGAAGTCAGAGA[A/C]AAAGTAAGTTATGCG | 11124 |
rs534855629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908503 | TATTATTGTTTGGGC[A/G]TCTAAGTCTCTTTGT | 11124 |
rs534876521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50712549 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGTATG | 11124 |
rs534877147 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50921534 | TGTGAAGTCAACAAG[C/T]GCAGATCATTTGAGC | 11124 |
rs534894768 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50931293 | TTTCTTATCTGCATT[A/G]TTTATACTTTCTTAT | 11124 |
rs534897002 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50676368 | GCCAAGATCACGCCA[C/T]TGCACTCCAGCCTGG | 11124 |
rs534903198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50566752 | ATTAGACTTGTTTTG[C/T]CTTTTCTGAACATCA | 11124 |
rs534920826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884715 | GGATACTGAACTGTA[G/T]TTTTTTTTGGTTTGT | 11124 |
rs534922180 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50784333 | TAATAAATAATACAA[A/C]ATTCATCAATCTTTT | 11124 |
rs534930448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50607634 | ATGTGAACATAATAT[A/G]AGGAAAATTTAAGTG | 11124 |
rs534936358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50500377 | TATGATCAACACATA[C/T]GTTTGACAAAGGTGC | 11124 |
rs534937288 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50647567 | CAGAGTTGTTCCACA[A/G]ATGTCAAGTGAATGA | 11124 |
rs534940792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50575413 | ATGGTTGTATTTATA[C/T]AAACTATATCAGCTT | 11124 |
rs534945315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50458774 | GCATTTACTATGCTA[C/G]TGCTTTATGTGTAAC | 11124 |
rs534946539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50750023 | GCCTAGCATAGTACC[C/T]GGGCAGTATAGGTTC | 11124 |
rs534949126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50827594 | GACCCTGCCACATCC[C/T]CCTCTCCGAGAAACA | 11124 |
rs534953452 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50711931 | TAACACTTAACAAGC[G/T]CTACCACATACCAGG | 11124 |
rs534957564 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50747633 | GACTTTGGAGGACTG[A/C]TGAGAAGGGATGATT | 11124 |
rs534960761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756943 | GGAAGGGACACAGCC[A/C]AACCATATCATCATG | 11124 |
rs534966277 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50659789 | AACAGATTTTCTAAT[A/T]TGCATTCAAGATTTT | 11124 |
rs534966282 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787126 | TCAAATGTAAGTTCA[A/G]CATAGTTAAACTATA | 11124 |
rs534968857 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50575069 | ACCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 11124 |
rs534970926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616599 | TTTCTTTGTGGCTAA[G/T]GTAAATGGGATTGTG | 11124 |
rs534973569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50450639 | TCCTAACAACTAATC[A/G]TCTATTTTCTTTAAT | 11124 |
rs534973864 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50934751 | GTGACTGAAAAAATT[C/T]TAAAGTCTTCACTTT | 11124 |
rs534974389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50502618 | TGCTCAGTGGCTGCT[A/G]GAGGCTGGACTTGCC | 11124 |
rs534988255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50616050 | TATAAAATTTAAGGT[A/G]CCTAGTTCCATTCCT | 11124 |
rs534989177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772602 | ACTAACACAGGAACA[A/G]AAAACCAAATATTGC | 11124 |
rs535000049 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50813356 | TCACTGAGAGGAAAA[A/C]CATTGCTAATATTTT | 11124 |
rs535020626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50661513 | AAAAGTACCCTGAAA[C/T]TACAGCCATCCATCT | 11124 |
rs535037100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451325 | ATGGTAACAAGAGCT[A/T]ACATTTATTGGGAGC | 11124 |
rs535041968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559254 | AGACTCCGTCTCAAA[A/T]AAAAAAAAAAGGATA | 11124 |
rs535044155 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50506618 | TGTCTCTCACTAGAC[A/T]GTGAGTACTTAGCTG | 11124 |
rs535059148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872376 | GAAGATATGCATGAA[A/T]TGCTGCAATCTTATG | 11124 |
rs535064031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50813810 | TCCACAGCTTCATTT[A/T]AAAAAAAAAAATGAC | 11124 |
rs535064701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714297 | TACTTGAGGTCAGAC[A/G]TTCAAAACCAGCCTG | 11124 |
rs535065557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725098 | CATCCTCTCCATCAG[C/G]TGCTTGCCCGGCCAT | 11124 |
rs535074078 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50870693 | TGCCCACAAGACAAT[A/G]AACTTCATCAATAAA | 11124 |
rs535074391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50769338 | GCCCAGGACCAGATG[A/G]GCTCACAGTTGAGTT | 11124 |
rs535078663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50707120 | AGGCAGAGGAATGGC[A/G]TGAACCTGGGAGGTG | 11124 |
rs535079155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806868 | GAAGACAAAAGCAAA[A/C]AAACAAACAAACAAA | 11124 |
rs535103221 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50624623 | AACAGAGGGCTTCAA[C/G]ATATGAAAAGGAAAA | 11124 |
rs535123148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620218 | AGCCTAGATTTGGTC[A/T]CTTAACATAATCCCA | 11124 |
rs535125318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50697960 | ATACACAAGACACAT[C/T]AGACAAAAGAAAAAT | 11124 |
rs535133146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50954064 | TGCCATTCTCCTGCC[C/T]CAGCCTCCCGAGTAG | 11124 |
rs535135098 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649880 | TGAGGAGGGACAATT[A/G]CTTGAACCTGGGAGG | 11124 |
rs535137179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601746 | TATACACACATATAT[G/T]CATATATACACATAT | 11124 |
rs535140121 | snp | A/G | 0.000545405 | 0.0165047 | intron-variant | FAF1 | GRCh38.p7 | 1:50612390 | GGTTCCGTTAGTGGA[A/G]AAACCTCATTATTTT | 11124 |
rs535148425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50717781 | CTGAGGTGGGAGGAT[A/G]ACTTGAGGCCAGGAG | 11124 |
rs535154798 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50905091 | CCACCCTGTGTCCAA[C/G]TGTTCTCATTGTTCA | 11124 |
rs535157914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653785 | GCAGGAGAATCAATC[A/G]CTTGAACCCAGGAGG | 11124 |
rs535159370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50612542 | CTCATGTCTAGTCAA[C/T]AGTGAGATGCCATTT | 11124 |
rs535161849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50710577 | AGATAATCCTTCACT[C/T]ATAGAACTATGAATA | 11124 |
rs535172858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551202 | TTTAAAGGAGGCAAA[A/C]TGTAAATGCTAAATG | 11124 |
rs535187330 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50564884 | TTCACCTTGTGTTTA[C/T]AAAATGTGTATTTTC | 11124 |
rs535203098 | in-del | -/CAGTGA | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50607767 | GTAGTCAATCATATC[-/CAGTGA]CACTCGGACAAATCT | 11124 |
rs535210771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50605603 | CAATAATCCACACTG[C/T]GAATTAAAATAGCCC | 11124 |
rs535216351 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50736544 | CACCTGAGTTCAGGG[G/T]TTTGAGACCAGCCTG | 11124 |
rs535217891 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50755042 | AACCATATCATTCTG[C/T]CCCTGGCCCCTCCAA | 11124 |
rs535218377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576260 | CATCATGTTTTTTCC[A/G]TATTAGACATAGGCT | 11124 |
rs535225899 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50928437 | TCAGCGGCATTAATT[A/C]TTTAGAATAAAAATA | 11124 |
rs535248475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50931952 | AAGACTGACTCCCAT[A/G]ATTCAATTACCTCCC | 11124 |
rs535252433 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50672919 | GTTTAGGAGTTCCAG[A/G]CCAGCCTGGGCAACA | 11124 |
rs535263641 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466152 | AGATTATAGTGGCTT[C/T]GGCTAGGGTTCAGTT | 11124 |
rs535280498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50732051 | TGACAAAGATGTATT[A/G]CTAAATACATTATTA | 11124 |
rs535299080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50470841 | CCATTTACTTCTGAC[C/T]TTGCTATTCTGCTTC | 11124 |
rs535305927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50828345 | ACGATCTTGGCTCAC[C/T]GCAAGCTCCACCTCC | 11124 |
rs535321170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512316 | TGAAGTCTTTGCCCA[C/T]GCCTATGTCCTGAAT | 11124 |
rs535334638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50724182 | GTTCAAGGTTACAAT[A/G]AGCTATGATAATGCC | 11124 |
rs535336308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50935691 | TTGGCCAGGCTGACT[C/T]GAACTCCTGACCTCA | 11124 |
rs535355078 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50924923 | AGGAGGCGGAGGCTG[A/C]AGTGAGCTGAGATCG | 11124 |
rs535365991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50668698 | CTCAAAAGCTCCATA[C/T]GACTGGCCTTTAATT | 11124 |
rs535369988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518787 | TTCTAGAATAATACC[A/G]AGCAGTAGGTTGCTG | 11124 |
rs535378564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876915 | CAACAAAGTGAAGTA[A/G]TATTGAATTACAACC | 11124 |
rs535386351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50580085 | AAAATAATAAATATA[C/T]AGTATACCCTAAATG | 11124 |
rs535387704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773628 | TGGAATCTAAACATC[G/T]GAATCCACATATGAA | 11124 |
rs535388510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50777604 | CCAGAGGTATCCTCA[A/G]TGCAGCTAAGAAAAT | 11124 |
rs535396173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921068 | ATAAGTAAATGTATA[C/T]AGTAACAAAATACAT | 11124 |
rs535399017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871692 | ACTATTCATTGACAA[C/T]GCACTTGGTTACTCA | 11124 |
rs535401785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50664183 | TTGTGTTTTTAGTAG[A/G]GACGAGGTTTCACCA | 11124 |
rs535410590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50958578 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATGG | 11124 |
rs535411685 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50672540 | TGCCTACCTCGACCT[A/C]CCAAAGTGCTGGGAT | 11124 |
rs535413077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50716899 | GCTTTGCTCTTTTGC[C/T]CTTCACAATAAATCT | 11124 |
rs535424472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523514 | ATTTCCCCAAAGACT[A/G]CTGACATTGAGCATC | 11124 |
rs535430257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50778637 | AGTGAAAGTGGATCA[A/T]CTTCCTCACTGTCTT | 11124 |
rs535430288 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50787576 | TTCTTAGCCTCCAGA[A/T]ATGTGAGAAAATAAA | 11124 |
rs535430822 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50722604 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 11124 |
rs535433896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50563329 | CCAGCTACTCAGAAG[A/G]CTGAGACAGGATGAT | 11124 |
rs535435138 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50680915 | TGAAGCATAGAATTT[A/T]AGCAAACCAATTAAA | 11124 |
rs535445940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50928662 | ATGGCGGGCGCCTGT[A/G]ATCCCAACTACTCGA | 11124 |
rs535453771 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50813985 | TATATATATACTATG[-/T]TTTTTACCTATACAT | 11124 |
rs535465307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937426 | GGGGCGGGGCGCAGA[C/T]TCTGTATAGGTCCAG | 11124 |
rs535468138 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50629004 | AATAATAGCCTTCAG[A/C]TCATAGGGTTGCTGG | 11124 |
rs535471040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50636646 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCTTGTTT | 11124 |
rs535471814 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50787451 | TTCTGGTTTCTGTCA[C/T]GTGAGGACACAATGT | 11124 |
rs535486757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50546660 | TGAGATACCGCGCCC[A/G]GCCATTAATTTGTTT | 11124 |
rs535491222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50817460 | AGAGACAGACAGCAA[A/C]ATGTTGGTTGCCAGA | 11124 |
rs535495212 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50555064 | TCTACAAAAAAAAAA[A/T]AATAATAGCTGGGCA | 11124 |
rs535498916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50863868 | AGCTACTGATTATTG[C/T]CACAATTTCAGAGCC | 11124 |
rs535503401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50809757 | AAGAAAGACTCCTCC[C/T]TAACTCACTGTTTGA | 11124 |
rs535508233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50627916 | ACATGGCAGTCATTC[G/T]TACCTAAAGAAAAGC | 11124 |
rs535511380 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FAF1 | GRCh38.p7 | 1:50907015 | GATATTGGCTGTGGG[G/T]TTGTCATAAATAGCT | 11124 |
rs535511398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50604315 | CTCTTAAACTTCTAT[C/G]AGTGATCCCACCATC | 11124 |
rs535515260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956984 | TAAATAAATTACCTG[A/G]TTTTCTTATAACTGA | 11124 |
rs535522157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50490446 | GGAAGGAAGGAAGGA[A/G]GGAAGGAAGGAAGGA | 11124 |
rs535538228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855644 | TGATGGATTATTCAA[A/T]ATATTTGTTTCATTT | 11124 |
rs535543228 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50819702 | ATATACATATATATA[C/T]ACATATATATATACG | 11124 |
rs535545059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50673402 | ATGAGCATCCATTCC[A/G]TTGTGCAGCAGGCAA | 11124 |
rs535556550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50826460 | GAGGCCAAGGCAGGA[C/G]AATCACTTGCACCTG | 11124 |
rs535559618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50507246 | CCCTGCCAAATTTGT[A/G]GACACAGTGATGTCA | 11124 |
rs535561697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50802106 | TATTCTTTTTTTTTT[C/T]TGAGATGGAGTTTCA | 11124 |
rs535565889 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50738775 | CAAGACTTGTATTTG[A/C]TTTAATTTTGAGGTT | 11124 |
rs535569841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50447211 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 11124 |
rs535574914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50509230 | CTGTCTGTAGTGAAA[A/G]AGAGAGAGAGAAAAA | 11124 |
rs535579335 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50823331 | GAACTGTGCTGGGTA[C/T]TGTGAATAATACATG | 11124 |
rs535581647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50674167 | CATGTTGGTCAGGTT[A/G]GTCTCGAACTCCTGA | 11124 |
rs535592377 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50578031 | AACACTTTATCAAAT[A/G]TAGTGTTTTACTTAG | 11124 |
rs535604259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50521186 | TGGTGAGAACTCACA[C/T]TATTTTTTTAATGTC | 11124 |
rs535605679 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50485802 | GAGGCCTCAAGAAAT[C/T]TACAATCATGGTGGA | 11124 |
rs535608878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50530443 | CCTGCTTTAAAGAAA[A/G]CAGCAATAACTCATG | 11124 |
rs535609071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516769 | AGATATCTACAGCTA[C/T]ACATTCAAATTTATC | 11124 |
rs535619661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771329 | CAACCTACAGAATGG[G/T]AGAAAATATTTGCAA | 11124 |
rs535622768 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50492755 | ATATATGCTTACTCA[A/C]GGCTGAATATATGCT | 11124 |
rs535628801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50934760 | AAAATTTTAAAGTCT[C/T]CACTTTTGGTTTTGA | 11124 |
rs535636319 | in-del | -/A | 0.24932 | 0.249999 | intron-variant | FAF1 | GRCh38.p7 | 1:50649785 | CTCTACTAAAACTAC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs535637439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50571581 | CATGAAAATGTATTA[A/G]AGATTAAGCAGCTCC | 11124 |
rs535640298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650051 | GCACTCTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 11124 |
rs535640928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50907661 | GATTTTCTAGTTTTT[C/T]TTCATAGAGTTGTTT | 11124 |
rs535642757 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50897916 | TTTGATTTATCTGTG[A/G]TCTCATCAGAGGATA | 11124 |
rs535651043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50529391 | AACAATCAATGCAAT[C/G]AATCCTTATTATCTA | 11124 |
rs535654757 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50902136 | GTCAGATAGAGGTGA[A/T]CAGTTGATTACTGTA | 11124 |
rs535676264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927305 | CTGCATGGGGACCAA[A/G]CGTGGTGGCTCACAC | 11124 |
rs535677674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579297 | ATGTGTGAGGTATAC[A/T]TAGTATATCTTACAG | 11124 |
rs535685401 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50753169 | TGCCCCTTGGTAATT[C/T]CACCATACCATCCCC | 11124 |
rs535692399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749160 | TATACCAAACACATA[C/T]AAACATTGCCTTTTT | 11124 |
rs535696828 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50617944 | TCTAATTTGTGTGCA[C/T]AGAGTTGTTCATAGT | 11124 |
rs535697256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453584 | ACATTTCATCTACCC[A/C]AAAGCTTATAAAACT | 11124 |
rs535704839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50803042 | TAACATAGACAATAG[A/G]TACCACAGAACCCTG | 11124 |
rs535712268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644047 | GTAACTTCCATGTCT[A/G]TTTCTTTTGACTGAC | 11124 |
rs535718420 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50809866 | ACAGATGCAAATATC[C/T]TTGACAAAATACTAG | 11124 |
rs535724180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50490533 | GGTAGGTTAACAGCT[C/T]CAGTATCAAATACAA | 11124 |
rs535729354 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50522464 | TATCTAACAAAGTGC[-/T]TGGCCCTAGCAATTC | 11124 |
rs535731025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777090 | ATAGTGAGACCCCAT[C/G]TACAAAAATGATAAT | 11124 |
rs535742275 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704632 | ATAAAATACTCATTA[C/T]GGAGGTTGAAAATGA | 11124 |
rs535743338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50679282 | CTGCCTATGGAGTAA[C/T]CATTCTTTATTCCTT | 11124 |
rs535746057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50768338 | TTAAGATAACCACAC[A/G]ATAATAGTAGACTTC | 11124 |
rs535754228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50787017 | GGAAAACAGGGAAAT[A/T]TCCAGAAACATCTAG | 11124 |
rs535765520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927783 | GTGTCAGCAGTTTGC[A/G]TGTCTTCTGGGGCCT | 11124 |
rs535772770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894862 | CCAAAACCTATGGGG[A/T]TACAGCAAAAGCAAG | 11124 |
rs535774315 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50803850 | ACAGCAAACTCTGTA[C/G]ATAAATAAATAAAAT | 11124 |
rs535780574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50482292 | CATGTTGTTGAATAT[A/G]TCAGTAGTTTGTTTC | 11124 |
rs535782052 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50672033 | TCTTTTTTTTTTTTT[A/T]ATTATTTATTTACTT | 11124 |
rs535785147 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50521127 | AGAATGGCTATATTG[A/C]GCTAAGTAACACATG | 11124 |
rs535791952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687323 | ACAAAGTCATACAAC[C/T]ACCTTAACCAATTCC | 11124 |
rs535795640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833903 | GATCACATTCCAGGC[A/G]CTCATGAAACCACAT | 11124 |
rs535803038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541639 | CTTGTTGCTTTCACA[C/T]CAATGGATTAATTAA | 11124 |
rs535805328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50683670 | GGGTGCAGTGGCTCA[C/T]ACCCATAATCCCAGA | 11124 |
rs535812953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582063 | GGGTGGGCAGGGGCC[C/T]AAAGTGACTTTTGGG | 11124 |
rs535837064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932294 | AAGGCAAGTCCCTTC[C/T]ACCTATGAGCCTCTA | 11124 |
rs535840460 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50499630 | TTAGAAATGTGGAAA[A/G]TTCTAAGGATTCTAC | 11124 |
rs535847191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526655 | ACAGTCATGTACAAA[C/T]GTTTACATGGACACA | 11124 |
rs535857081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50734715 | CTCCAGCCTGGGCGA[C/T]AGAGCGAGACTCCAT | 11124 |
rs535858049 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50713901 | GGCTCAGCCTCCCAC[A/G]TAGCTGGGTTTACAG | 11124 |
rs535861322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726070 | CCAGCCTGGCCAAGA[G/T]GGTGAAACCCTGTCT | 11124 |
rs535865076 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50601405 | TAGGCTGGGCGTGGT[G/T]GCTCGGTGTGAGACA | 11124 |
rs535870766 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50791462 | GAGACACTATCTAGA[C/G]ATTAGTAGTTAAAGA | 11124 |
rs535873120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50932904 | CACCCGGAGGCTCAA[C/T]ACCATGTGGAAGCTG | 11124 |
rs535885848 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575263 | TTTAAGAAATAATTT[G/T]AATATGGGCACTAAA | 11124 |
rs535885913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50825812 | AAGGACTGAAATCAC[A/G]TAGTACATTTTCTAA | 11124 |
rs535904753 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50574197 | TTGGGTATAGATCTT[G/T]ATCAGTTTTCATTGC | 11124 |
rs535907622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50568882 | AGACAGCTTGTAATG[C/G]GAATAAGGGCAGGAC | 11124 |
rs535919449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50847890 | AAATGCACACATATA[C/T]ACACACACACACACA | 11124 |
rs535927248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726601 | TTGGGAGGCTGAGGT[A/G]GGCGGATCACAAGGT | 11124 |
rs535931883 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50864035 | GTTTGTATTTCTGTG[G/T]GATCAGTGGTGATAT | 11124 |
rs535932013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50577755 | GATGAGTGTCCTTCA[C/T]AGTTAAGGGCAAGGA | 11124 |
rs535935630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50517539 | ATTATCCCCATTTTA[C/T]TTAAGAGGAAATTGG | 11124 |
rs535936034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632492 | ATTGGGAACACATCT[A/G]TTCTTTTTAATCTCT | 11124 |
rs535936311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50722114 | TTAGCCACAGGAGTC[C/T]CCCACTGGCAATTGC | 11124 |
rs535938690 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50676913 | TTTAACCAATATGCT[A/G]TGCTGCCTCTCTCCA | 11124 |
rs535954135 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50621906 | CACAGTGGCTCACGC[C/G]TGTAATCCCAGCACT | 11124 |
rs535955859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50774109 | AATTGATGGCACGGA[A/G]GCAACAGACATCAGT | 11124 |
rs535959293 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50620031 | CTCCTGCCTCAACTT[C/T]CCAAGTAGCTGGGAC | 11124 |
rs535959699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684535 | GGGTTACAGACATAC[A/C]ACCAATGATATACCG | 11124 |
rs535974926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50677692 | CTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGACC | 11124 |
rs535993704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758415 | AAATCTGTCTTACGA[A/C]AGAATACTTCTAGTT | 11124 |
rs535999908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50670036 | TGAGGGAGGAGAATC[A/G]CTTGAACAAGGGAGG | 11124 |
rs536000360 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50748006 | AGCCTGCAGAACTGC[A/G]AACCAATTAAACCTT | 11124 |
rs536000824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748428 | CTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG | 11124 |
rs536010945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50904837 | AAAAAAATACATTAT[C/G]AATATCTTTTAAGCC | 11124 |
rs536021333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50751535 | TTTTAGTAGAAACAG[A/G]GTTTCACCACGTTGG | 11124 |
rs536035860 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50806106 | CTAGGAAAAAGTATT[G/T]ATAATACATGTATCT | 11124 |
rs536046153 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50525445 | TTGTTTTAAGCTCAG[-/T]TTTTTTTGTTGGTGT | 11124 |
rs536047734 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50649661 | AATCAAGAAAGAAAA[C/G]TCTGGGCACAGTGCC | 11124 |
rs536048222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848149 | TACCAAAAAATAATT[A/T]AAAAAAAACAATGGA | 11124 |
rs536052828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50905221 | GGACATGAACTCATC[C/T]ATTTTTATGGCTGCA | 11124 |
rs536055705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50951195 | GCCAAGATCACGCCA[C/G]TGCACTCCAGCCTGG | 11124 |
rs536063028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653722 | CATACAAAAATTACC[C/T]GGGTGTGGCGGCAGG | 11124 |
rs536063218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50646459 | GATGTCAACTTTGTG[A/G]AGCACTGAACAATTT | 11124 |
rs536068487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50741360 | ATGGAAAGTGAGAGT[A/G]AGAAAGGCTCAAGAT | 11124 |
rs536081385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50797414 | AAAAAAAGATATTGA[C/T]TGAATGCCAGGTGTA | 11124 |
rs536081767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744559 | CTGATTCCTTAAACT[A/G]AATTACTATTGCCAA | 11124 |
rs536082883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50794153 | CACACCACAAAAATA[A/C]AAGGGCTGCCACCTT | 11124 |
rs536086404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848642 | AATAACACATATTGA[C/T]ATCATATACCTCCTG | 11124 |
rs536088423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50703327 | TACATACTTAAGTGT[C/T]ATTGTGGATTGAATA | 11124 |
rs536102145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50696616 | TCATCTAAATGGATA[C/T]CATATATCTCTGGAT | 11124 |
rs536105554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944429 | TAAGATGGTCCCTCC[A/T]CCAAGTGTCAGGATT | 11124 |
rs536109399 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50717742 | AATGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 11124 |
rs536126595 | in-del | -/AGTT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50728407 | AGCGATAAAAGACGA[-/AGTT]AGTTAGAGAGAAAGA | 11124 |
rs536136605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50597958 | GTCCTGAGTTCAAAT[C/T]CACTTCTACTATTCA | 11124 |
rs536138124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50897038 | TGGAATTTCAACACA[C/T]TTCAACACAACACTA | 11124 |
rs536139058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689347 | CCCAGCACTTTCAGA[A/G]GCCGAGGCGGGTGGA | 11124 |
rs536148288 | in-del | -/C | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50915348 | GCACTCCAGCCTGGG[-/C]AACAAGAGCGAAACT | 11124 |
rs536160196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50751035 | TTTCTTATTTACTAT[A/G]CTAATATGGGGATGT | 11124 |
rs536169314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50936945 | GAGTCAGACGAAGCA[C/G]AGATGCAGAAGCCAA | 11124 |
rs536174372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841696 | ATTTTGAAGTAGCCA[A/G]TCTGTTAACATGGCA | 11124 |
rs536179164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50535035 | CCATAAAACTGAGTG[A/C]TAAAATCCATATAGT | 11124 |
rs536183541 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50829538 | TTCCTTAACACATTC[C/T]ACAAAAGGAAAACAG | 11124 |
rs536188181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50540771 | GACCAAATGCAAATA[C/T]AGAATGCTTTAATAA | 11124 |
rs536190615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50890298 | ACAGCACACTGATGG[A/G]TCTTGACTCTTTATC | 11124 |
rs536192628 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50544261 | AGGAAAACAGAGTAT[A/T]TGACTAAGCTAGGGG | 11124 |
rs536198373 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50593274 | CACTGCTCTTCACTA[C/T]ATGGAACTGACTTCT | 11124 |
rs536205007 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50603029 | ACACAGAATAAGAAG[C/G]TTGCCCAAAGTCAAA | 11124 |
rs536207338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50845997 | GGCGTGGTGGGGCAC[A/G]CCTGTAATCCCAGCT | 11124 |
rs536212008 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50918255 | GTGCAGGTTAGTTAC[A/C]TATGTATACATGTGC | 11124 |
rs536233538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545906 | AGTAGCTCACACCAG[C/T]AATCCCAGCACTTTG | 11124 |
rs536241143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955785 | TATGGTATATACATA[A/C]AATGGAACATTATTT | 11124 |
rs536244067 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50877268 | GTACTTTACCTCTGT[G/T]GTCTTCCTTCCCAAG | 11124 |
rs536244558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468673 | ACCATCTTGGCCAGG[A/C]TGGTGTTGAACTCCT | 11124 |
rs536253925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50737825 | GGGGGAAAGCTTGAC[A/C]ATGTTCAAAATTTAG | 11124 |
rs536261348 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846431 | TCGCGTCCTGGGAAC[C/G]AGCTCGCTTCCGAGC | 11124 |
rs536263691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50553120 | AAAACTGGATATAGG[A/G]AAGGGTAGATGGGGT | 11124 |
rs536267237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50890862 | CTCTCCCTGAGGATT[A/G]TCTTTGTGACGTTCT | 11124 |
rs536278058 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50729940 | GCAGGAGAGTTGCTT[A/G]AACCCAGGAGGCAGA | 11124 |
rs536278942 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50700528 | AAGTGCATATTGTAA[A/T]ACAGGATTATTACAG | 11124 |
rs536280294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50854182 | TTTATTCTCCCCTGA[C/T]CCAAATTCTTCTATA | 11124 |
rs536282550 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468235 | ACAACAACAACAAAA[A/C]TGCATCACATTGTAC | 11124 |
rs536308894 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FAF1 | GRCh38.p7 | 1:50942134 | TAACAACAATGGCTG[G/T]TACAAATTAGATGGC | 11124 |
rs536320810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50479875 | CAGCAACCTTGAGAT[C/T]TGAATATCCAACAGT | 11124 |
rs536321618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624102 | AGACCACGTAGTTCC[A/G]TGGCAGGCAGTCAAG | 11124 |
rs536324398 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50495219 | TTCACTCTTTCCATA[C/T]TTTTTGTACCTATTA | 11124 |
rs536343695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513106 | AGATGGTGGGACTCT[A/G]CTCTGAAATGTACTA | 11124 |
rs536356299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624741 | CATATCTCTAACTTT[A/T]CACATATATTCCCTT | 11124 |
rs536358305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50617264 | CCATTCAGTATAATG[C/T]TAGCTGTGGGTTTGT | 11124 |
rs536364920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50838662 | ACCAGCTGCTCCCAC[A/C]GATGTTACTGGGTTT | 11124 |
rs536367289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691992 | AGGCCCAGGCGGGCA[A/G]ATCACTTGAGCCCAG | 11124 |
rs536372976 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50588045 | TAATCCCAGCACTTT[C/G]AGAGGCCGAGGCAGG | 11124 |
rs536377547 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50628509 | TGGGGATATTTAATA[A/T]CATTTCTTAAGTTTT | 11124 |
rs536381563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50747386 | GAGATTATTTGGAAC[A/T]TTAAGATTTAATGAC | 11124 |
rs536392472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50878403 | TAGGATTCTAGTCAG[A/G]TAACTCACAACCTTT | 11124 |
rs536399714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50918582 | CACATTTTCTTAATC[A/C]AGTCTATCATTGTTG | 11124 |
rs536403317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50926409 | GAGTATACAACTGTA[A/G]ATATTGGAGACTGGG | 11124 |
rs536407816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50513447 | GTGAGATGAGATCGC[A/G]CCATTGCACTCCAGT | 11124 |
rs536411504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822317 | AAATTAAACACAAGG[C/G]AATATGAGGCAGATC | 11124 |
rs536417160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910060 | GTACAGACGGGGTTT[C/T]GGTGTGGATGTCCTT | 11124 |
rs536421411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543649 | TATCATCATTTCTTT[C/T]AGGATTAAAAATGAT | 11124 |
rs536432213 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50739702 | GCCAACGATTTTATA[C/G]ATGGGAAGCTATATA | 11124 |
rs536436637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560949 | GGAAACAGATTAATA[C/T]TTACTATGCTGGTGC | 11124 |
rs536440968 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50860781 | AAAAGACAAATTCAC[G/T]CACACGTTAATCGCA | 11124 |
rs536443047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50946919 | CATTATCTCTATCTT[C/T]CAAGGCTGTTAGGAA | 11124 |
rs536443741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851186 | TCCAGGTTCAAGTGA[C/T]CCTCCTATCTCAGCC | 11124 |
rs536448345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823031 | TGCCCGCCTCGGCCT[C/G]CCAAAGTGTTGGGAT | 11124 |
rs536449031 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50488513 | GTGTGCATGTGTGAA[C/T]GACAGCATAAAGGAG | 11124 |
rs536450403 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50445047 | TATAGTCCAAGCACT[G/T]TAATATAAAAGGTAG | 11124 |
rs536459651 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50776496 | AAGCCAGCCATTTCT[G/T]ATCACCACACTCGAA | 11124 |
rs536465588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550488 | AAAGCTTTCAAGCAA[G/T]AGCTGATTGTAACCC | 11124 |
rs536469815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751939 | AGAAAAGCCATCTAG[C/T]GTTTCAGGTTTTCTT | 11124 |
rs536471497 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50583068 | AATAGAAGGAAAAAA[C/T]TGTTTCTTTTAAAAG | 11124 |
rs536475401 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50570148 | TAGAATAAGCCTCTA[G/T]CTCCTAGAGAGACAG | 11124 |
rs536480536 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707002 | AGGTCAGGAGATCAA[C/G]ACCATCCTGGCTAAC | 11124 |
rs536480638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851759 | GATACAACAGGTAGA[A/G]CAAGATCCAATGTAA | 11124 |
rs536485696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50493885 | AAAAAACGGACCTTC[G/T]AAAAGCAATCACAGC | 11124 |
rs536487333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910689 | ACCCTCCAAGCCAGG[C/T]GCGGGATTAATCTGG | 11124 |
rs536498821 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50601118 | GAGAAGACAAAAAAG[C/G]TCTTTCAAAATCTTA | 11124 |
rs536503513 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50715907 | TTTATATATATGAAC[A/G]TACAAAGCCATATAT | 11124 |
rs536507503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807533 | TAAATCCACCCCCAT[A/G]GTCCAATCACCTCCC | 11124 |
rs536507659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50861776 | TGTTTCAAGCTTGAA[A/G]GACTAGAAAGGAAAA | 11124 |
rs536510624 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FAF1 | GRCh38.p7 | 1:50815612 | TTTTTAAGTTCTTTG[A/G]GAAATCTCTAAACTG | 11124 |
rs536521728 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50831515 | ATATCTGCCGTCTTT[A/C]TCTACACCGTCCCCT | 11124 |
rs536524100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50767406 | TTAGGATATAATTCG[C/T]GAAAATTTCCCCAGC | 11124 |
rs536537127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50592702 | CCTGTAACCCCAACA[C/T]TTTGGGAGGCCAAGG | 11124 |
rs536550807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486537 | TTTTTTTAAATTCAC[A/G]TCTCTACGGGCGCAC | 11124 |
rs536559948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50611164 | TGATTCACTTTGTTA[A/G]TTCTTTTGTGTCAAG | 11124 |
rs536574174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50593169 | TAATAAGATATTACC[A/G]AGGTTGTGAATGTTT | 11124 |
rs536577642 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50811157 | GTGAGCAACATGGCA[C/T]AACCCCGTCTCTATA | 11124 |
rs536585072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50955227 | AGAACAGTTATTCTA[C/T]AGTTACAAAAAGACT | 11124 |
rs536592717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50663012 | GAATTTGTATCTTTA[A/G]TAAAAGGTCAAACCT | 11124 |
rs536611367 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50440863 | CTTGCATATATGTCA[A/G]ATTCAGTCCTCAAAC | 11124 |
rs536614049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906069 | TATAAGGTGTAAGGA[A/G]GGGATCCAGTTTCAG | 11124 |
rs536617080 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50925110 | GCTAAGAATACACAT[G/T]GGGAAAACAACAGTC | 11124 |
rs536620411 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50811164 | ACATGGCATAACCCC[A/G]TCTCTATAAAAAAAT | 11124 |
rs536624523 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50683136 | ACAATAGATGTTACA[C/T]AGGATGGTTAGAAAA | 11124 |
rs536630219 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50730481 | ATTTCTGCTCTTTAA[-/TCTT]TCTTTCTATTTTCAG | 11124 |
rs536637553 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50675037 | CAGGGATTACAAGTG[C/T]CCACCACCATACCTG | 11124 |
rs536640058 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50640586 | CAATTTTTAAAATTA[C/T]ATTTGGGCTTTTCTA | 11124 |
rs536640549 | snp | A/G/T | 1.71971e-05 | 0.00293227 | intron-variant | FAF1 | GRCh38.p7 | 1:50857881 | ATTAAAGACATTCAA[A/G/T]AATTCATAAAATTTG | 11124 |
rs536649482 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50846355 | AAGCATGCTTTTGCC[A/G]CCCAGGAGACGTCAG | 11124 |
rs536667517 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50545361 | CTTACTGCAACCTCC[A/G]CCTCCCGAGTGATTC | 11124 |
rs536667900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648714 | GGCGGATCACCTGAG[A/G]TAGGAAGTTCAAGAC | 11124 |
rs536672451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749913 | TTCACGAAAAATGTT[C/T]TGCAGAGTGCCTAAT | 11124 |
rs536677220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849521 | GAAAAAAATAAGTCC[C/T]AAAATTCAAGCATAG | 11124 |
rs536677650 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50604580 | TGGTACAATCACGGC[C/T]GACTGCCACCTCGAT | 11124 |
rs536685045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50804086 | CAGGAGAATATCAAT[A/T]GTTCATATAATAAAT | 11124 |
rs536685401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50799915 | TCTGGTCAGTAGACA[C/T]ACAAGAGGAATTTTC | 11124 |
rs536692563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50496603 | GAGGTGTAAAAGTTA[A/T]CTCTGGGGACCAAGC | 11124 |
rs536715581 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50918571 | TGTATATGTGCCACA[-/T]TTTCTTAATCCAGTC | 11124 |
rs536728388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50874114 | TTTGGTTCTAGTACC[C/T]GACAATTGTCTATTT | 11124 |
rs536730441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694721 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTCA | 11124 |
rs536731293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50691514 | CCCAAAGTACTGGGA[C/T]TACCGGCATGAACCA | 11124 |
rs536731403 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50914981 | CCCAAATCAGCTCTC[A/C]ACATTGCAAAGTTTT | 11124 |
rs536732043 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50503598 | CCAGCCTGGGCAACA[G/T]AGTGATTCCCTGTCT | 11124 |
rs536732454 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50958633 | CAATGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 11124 |
rs536736000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598760 | TGGATCACCTGAGGT[C/T]AAGAATTCGAGACCA | 11124 |
rs536741079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50792942 | ATGTACAAGACCTGC[A/G]GAGACCTTTAGAAGT | 11124 |
rs536753010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50484006 | TTAGATATTCAAGTC[C/T]GGAGTTCAGGGAAAG | 11124 |
rs536753257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50783929 | ATACACCACATTAAA[A/G]GCAAGAAGGATAAAT | 11124 |
rs536758176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50479058 | TGCAGTTTAAAAAAT[G/T]TTAATTAAATGCAAT | 11124 |
rs536758980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50793532 | GAAAAAAACACACTC[A/G]GTAACTGGTAGATAT | 11124 |
rs536771445 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50894316 | AATTAAAAAAAAAAA[A/C]AAAAAAAAAAAAAAC | 11124 |
rs536772911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50942750 | TTAGTTGTCGTTGTT[G/T]TTTTTTTTTTTACAG | 11124 |
rs536782104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895555 | TAGCAAAACCAAAGA[A/C]ACATCAAAAAACAAA | 11124 |
rs536784651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742764 | TTTGGTGTTTTCTTT[A/C]TGTCAAGGTTGTTGA | 11124 |
rs536785238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50537963 | TCAATGAAATCTGTG[C/T]ACTCTGTTACATTAA | 11124 |
rs536785485 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | FAF1 | GRCh38.p7 | 1:50739411 | ATGTGTATGTGTATA[C/T]ATGTGAGTGTATGTG | 11124 |
rs536789586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50892237 | GTGGGAGTGACCCAA[C/T]TTTCTAGGTGCCATC | 11124 |
rs536797772 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50548051 | TCTAGCAATGCAAAG[-/A]AAAGATTCACTTTCC | 11124 |
rs536816831 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704300 | TTGAGAGGGTGGCAG[C/T]AAAATTATGGCTAGA | 11124 |
rs536820101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50673269 | CTCAAAAAAAAAAAA[A/G]AAAAGAAAAAAGAAA | 11124 |
rs536821205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50766654 | CAGCACAGGGCTACC[A/G]TGCACAGGTATTCAT | 11124 |
rs536829445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50670543 | TCATTCTTATTTCAT[G/T]ATAGTCCTTGAACTA | 11124 |
rs536845728 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50447361 | CGATCTCCTGACCTA[A/G]TGATCCGCCCGCCTC | 11124 |
rs536859878 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50882986 | AGACTCTTGTCTCCA[-/A]AAAAAAAAAAAAAAA | 11124 |
rs536862674 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50568989 | TTTGTTGAAATGCTC[-/TT]TGTGTCAGGCTCAGC | 11124 |
rs536865767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662436 | TTTCTAAGAGATTAC[C/T]AGGATGATGATAGTA | 11124 |
rs536875020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50573657 | TGGAGAGGTTCCAAA[A/G]AGAAAAAGTCAGCTA | 11124 |
rs536888457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618254 | TAATTTTAGAGCTTT[C/G]TAACTAATTAATGAG | 11124 |
rs536889777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50718838 | ATTTTTATCTCTTTA[A/G]CTACATCAAGATTTT | 11124 |
rs536893362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50826368 | CCAGCTTAGCCAACA[C/T]GGTGAAACCCCGTCT | 11124 |
rs536895399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50922265 | AGGAGTTCGAGACCA[A/G]CATGACCAACTGGCA | 11124 |
rs536898446 | in-del | -/TAAAA | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50550737 | TTTTAAAAAACTATT[-/TAAAA]TAATCTGTCTTCTGC | 11124 |
rs536902431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50552082 | GGCGGATCACCTGAG[A/G]TCAGGAGTCCGAGAC | 11124 |
rs536902943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50711177 | CCTCCCAAAGTGCTG[C/T]GATTACAGGCATGAG | 11124 |
rs536910329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870802 | ACACAATATTGAAAC[A/G]AGGCCAATTAATAAT | 11124 |
rs536911267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50819248 | TAGAAATCTTGATTG[A/G]GGGAGGGGGGATTGG | 11124 |
rs536915396 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50874318 | CATCCCATACCCTGG[A/T]ATACCCTCCATCAAC | 11124 |
rs536918297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50958159 | ATTAATTAATTGAAA[A/C]ATTTTTTAAAATGTA | 11124 |
rs536918679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50613470 | TTGCATTCTAATGTA[C/T]TTCATCTCTGTGGAC | 11124 |
rs536925874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50759311 | CCCCCTCCCCCCCAC[C/G]CCACAACAGTCCCCA | 11124 |
rs536927702 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50524531 | GGGTTTTCCATTTAA[A/G]TCTTCAATCTATCTT | 11124 |
rs536929433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610290 | ACCAAACTTTCAAGC[A/G]TTTTTCTAATTGTGG | 11124 |
rs536929807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50911326 | ATCTGCCTGCCTCGG[C/T]CTCCCAAAGTACTGG | 11124 |
rs536931577 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50895990 | CTAAGATTGGGAACA[A/C]AAGGATGCCCACTTT | 11124 |
rs536939249 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50815563 | CCTCTGGATATATAC[C/T]TAGTAATAGCATTGC | 11124 |
rs536954077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862636 | CAACCAAATATCTGC[C/T]GTCTTCAAGAGACTC | 11124 |
rs536964005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50711748 | GGGATTATAGGCATA[A/G]GCCACCACACCCGGC | 11124 |
rs536968383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602388 | TATTTGTATGTCAAG[A/G]TGTATCCAACTGTAC | 11124 |
rs536976470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808113 | TATTCAGCATTCTTA[A/G]AGAAAAAAAATTCCA | 11124 |
rs536987199 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50760053 | GATTCTGGATACTCG[C/T]CCTTTGTCAGATGAG | 11124 |
rs537007233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50826054 | AGCCTTAATGATACA[C/T]ATTAAGTATGAAGAC | 11124 |
rs537007379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50536762 | TGGCACATGACAAAG[A/G]CTTTAATGAATATTT | 11124 |
rs537009810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50511091 | ATGTAAGGCTCTCCA[A/G]ATGCATTTAAACACA | 11124 |
rs537014372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908433 | GGATATTCTTGTTAA[C/T]TTTCTGTCTCATTGA | 11124 |
rs537015392 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50505019 | TGTAAGACTGTAGAA[C/G]TCTTCTGAGTGGGGG | 11124 |
rs537026338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50876131 | CCTACAGAAAATAAA[A/G]GTATGCATTCCAGAG | 11124 |
rs537028564 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50650623 | AGACTGTCTCAAAAA[A/T]ATATATAAATAAAAA | 11124 |
rs537028683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659044 | AAATTGAAATCATAA[C/T]CCTGCAGGGAAGAAA | 11124 |
rs537029065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50803258 | TGTGGTGCTGGAAAA[G/T]AAACAAAATACCAGA | 11124 |
rs537031346 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50934810 | TAAAATTCTAGTTGA[-/T]TTTTTTTCTTTCAAC | 11124 |
rs537033999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50720680 | CTCAACTGTCCTGAA[A/C]CCCCACCCTAGGAAT | 11124 |
rs537051133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50908890 | TTTAAGGTTAATATT[A/G]TTATGTGTGAATTTG | 11124 |
rs537063496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50651112 | CATAAGAGACTCAAG[A/T]TTATAAAAGAATTGA | 11124 |
rs537067721 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50796134 | AATACAGAATAAATA[G/T]TGAAAGAAGAAACTC | 11124 |
rs537069267 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50538315 | TACCCATACCTCCCA[-/T]TTGTGCCACATAAAC | 11124 |
rs537079591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50623410 | CTGTCTCTACTAAAA[C/T]ACAAAGAAATTAGCT | 11124 |
rs537097927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50752116 | TTGGGACTACAGGCG[C/T]GTGCCACCACACCCA | 11124 |
rs537106747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945145 | AATACCTTGACAATC[A/G]GTTCATTGCTGAGTG | 11124 |
rs537106851 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50714642 | TTTGACAGACCTATT[A/G]AAGAAGGAAAGGGGG | 11124 |
rs537112661 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50758586 | AAAAATGTGTAACCA[A/C]ATATTTACAATTTCT | 11124 |
rs537113415 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50813220 | ATGTAAAATAAATTT[A/T]AAAAAAAAGAAAAGC | 11124 |
rs537132977 | in-del | -/TTTG | 0.00636936 | 0.0560724 | intron-variant | FAF1 | GRCh38.p7 | 1:50643578 | CTCTAGAAGTGTTAC[-/TTTG]TTCTTTTAAAAAAAA | 11124 |
rs537133415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909543 | TGGTCTTTTCACATA[C/G]TCCCATATTTCTTGG | 11124 |
rs537133965 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50458459 | CATACAATAGGCACA[A/G]AAAGAAATAGCTATA | 11124 |
rs537135404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50493016 | ACCCTTTCAGTCATC[A/G]ATTAAAGGATTAAAC | 11124 |
rs537142899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50903856 | CCAGCATGTTCTCTC[C/T]ACAGGTTGCACATAC | 11124 |
rs537150164 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50895052 | CAGAAATAAATGCAA[A/T]TGAAACAAATAAAGC | 11124 |
rs537156826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50796543 | CTTTCCTTTGTGCCC[A/G]TTGGTGGTCAGCAGG | 11124 |
rs537161150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50787872 | ATAATCAGTATTGGA[A/G]AGTTACCAGTTTCAA | 11124 |
rs537164849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842565 | TACCTCTGCTTGGTC[C/T]TCTCCTCTAGGCACA | 11124 |
rs537170984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695361 | TGCAGCGAGCAGAGA[C/T]TGCACCATTGCACTA | 11124 |
rs537171911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50501625 | GAGATTGCACCACTG[C/T]ACTCCAGCCTGGGTG | 11124 |
rs537174415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50855483 | CATATCCGAGGTTAC[A/C]ACTCAATTAATGCAA | 11124 |
rs537181624 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50574284 | AAGTTTTTATGAATA[A/G]GGACATGAGAAGCTG | 11124 |
rs537183371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541479 | GGATGTATAGATCGT[G/T]AGATTAGAAAATTAG | 11124 |
rs537185026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50888878 | ATGATGCTGGCTTCA[C/T]AAAATGAGTTAGGGA | 11124 |
rs537185298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50750838 | ATGCAGGCCAGGCTG[C/G]TCTCAAACTCCTGAC | 11124 |
rs537189150 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50512577 | CTGAGGCCACTGTTC[C/T]GTTCCATTGGTCTAT | 11124 |
rs537191802 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50570965 | CAGTACCACAGAAAA[C/T]GAGTAAGAAAATGTT | 11124 |
rs537194006 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50507692 | CTGCCTTCTAGCCTG[A/G]GCAATAGTGTGAAAC | 11124 |
rs537196194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757731 | TTATTATAACATGAG[A/T]TCATTTATATGTATT | 11124 |
rs537196323 | in-del | -/AC | 0.00517822 | 0.0506191 | intron-variant | FAF1 | GRCh38.p7 | 1:50751991 | TTTTTGTTTTTTGAG[-/AC]ACAGTCTCACTCTAT | 11124 |
rs537206262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921685 | ACTAGGGAGGCTGAC[A/G]TGGGAGGATCACCTG | 11124 |
rs537207701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770502 | GAACACAATCTCATT[C/T]ACAGTAGCCACAAGG | 11124 |
rs537208809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591776 | CATCTCTTATCTTCC[G/T]TTTCCCCCGACTTTC | 11124 |
rs537209091 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50583261 | TCCAAAAGAAAAAAA[A/T]AAAGGAAAAAATTCA | 11124 |
rs537211218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50524549 | TTCAATCTATCTTGA[C/G]TTAATTTTTGTATAT | 11124 |
rs537220819 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50915718 | TCTTAACCTTCTTAC[A/G]AGAAAAAAGGTATGT | 11124 |
rs537221466 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50950520 | ATAAAGGTAAATGAA[C/T]GGGTATGGCTGTGTT | 11124 |
rs537227162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456021 | CGGAGATGGCAGTGA[A/G]CTGAGATGGCACCAC | 11124 |
rs537229090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50873506 | AGGACTTACTTCCCC[A/C]TCTGGGCAAGACAAA | 11124 |
rs537240909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50475014 | CACCCTCTGTAACTT[C/T]CCAGGGTAGTAAGAC | 11124 |
rs537245072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50743740 | CTCTAGAACTAACTC[A/T]TTTTTTTTCCTTCTT | 11124 |
rs537245938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50721461 | CTCAGGATCCGCCTG[C/T]GTCGGCCTCCCAAAG | 11124 |
rs537246715 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734858 | ATGTGAGTTGCTAAA[A/C/T]AGAGATTTGTAAGTT | 11124 |
rs537257165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50735879 | GTGCCACAACACCCG[A/G]CTATTTCATAAAAAT | 11124 |
rs537259002 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50918642 | ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG | 11124 |
rs537277069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50621061 | ACCCTAGTTCTCAGT[C/T]CTCTGATGGTGGGGG | 11124 |
rs537284860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50821242 | GTGTTATATGCCAGT[A/G]GAGCATAAATATCTG | 11124 |
rs537302692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467200 | AAATACAACTAAGAG[C/T]ATATTTTACCAGCAT | 11124 |
rs537314074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810788 | GCACGGTGATTCACA[C/T]CTGTAATCCCAGCAC | 11124 |
rs537314119 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50726454 | GTAATCCCAGCACTT[C/T]GGGTGGCCGAGGCGG | 11124 |
rs537315153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50629737 | ATAACATCTACCCTT[C/T]GGGATTGATTAACGT | 11124 |
rs537317444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771141 | TAAAACCTAAAACTA[C/T]AAAAACCCTAGAAGA | 11124 |
rs537318268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50727502 | ATCTACTATGTTTCC[A/G]ACACTTTTTTAGGTG | 11124 |
rs537320570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50865519 | AGCCATAAAAAATGA[C/T]GAGTTCATGTCCTTT | 11124 |
rs537337329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50779906 | TGGGCCGCTTAGTGA[A/G]AGCCTGTCTCTTAAA | 11124 |
rs537344425 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50771878 | TGCACGCTAGCCTGG[A/G]TGATAAGAGTGAAAC | 11124 |
rs537345771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50574458 | AGGACTTTGGTACAG[C/T]AGTCTCTTAAAAGTG | 11124 |
rs537349446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771933 | AAACAAAATGCCAAC[C/T]ATGTTTAATTTTGAA | 11124 |
rs537356636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50508956 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 11124 |
rs537359363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614400 | TAAATGTATTGAAAT[A/G]TTAGAGTTAAGGGGG | 11124 |
rs537373278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50781007 | CAGCTTAGCTGATTG[C/T]CAACTCACTGGCCAC | 11124 |
rs537381406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50762984 | ATGTAGGCCAGGCGC[A/G]TTGGCTCATACCTGT | 11124 |
rs537387417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50658109 | AGGTGTTCCACAAAC[C/T]GAGAGTGTTACGTTA | 11124 |
rs537389244 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50744936 | AAATAATATTATTTA[A/T]CTTATCTTGCCTTAG | 11124 |
rs537395190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884636 | GATTAATAACTTTTT[A/T]AATGTGTTGTTGAAT | 11124 |
rs537400001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50514699 | TAGAAAAGATTCTTT[G/T]TCATCTGGATAGAAG | 11124 |
rs537401138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50755704 | GCTTCTGCCTGGGCA[A/T]CCAGGCACTTCTACA | 11124 |
rs537408319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50776953 | CAGAGGAAGTTTGGT[A/G]ATTTAAAAAAAAATA | 11124 |
rs537412020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50767688 | AAAGAAATTCTAATC[A/G]AGAGCTTCATATCCT | 11124 |
rs537413670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50827499 | AACACTGCGGAAGGC[C/T]GCAGGGACCTCTGCC | 11124 |
rs537417012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50676030 | CTTCAAAAATCAGTG[A/G]GTCTTTTTCCTAACA | 11124 |
rs537424720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871113 | TTGCTTAAGCCAAAA[A/C]CTAATGCAGAGCAAG | 11124 |
rs537428583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880553 | ACTATCTCCACATGT[A/G]CACACCAAGGAAAGT | 11124 |
rs537431259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50558398 | GGTGGGGTCGGGGGA[C/T]GGGTTACAGAATGGG | 11124 |
rs537444735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50815935 | TGGGGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 11124 |
rs537447304 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50608372 | GCCTTGCACCTCAAT[A/C]GACAAAGGTTTTACA | 11124 |
rs537456846 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462110 | ATATATAAAAACTTG[A/G]GAGGTTGTGCCTGGT | 11124 |
rs537459569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50668591 | GAAACTGGCTCCAAA[C/T]GACAATTTAATTAAA | 11124 |
rs537469654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457946 | CGACCGGGCGCGGTG[A/G]CTCACACCTTTAATC | 11124 |
rs537473828 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50811706 | CATAATTAGAAAAGA[C/T]TATTTTAAAATTCAT | 11124 |
rs537478591 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50612166 | TCTTCATTTTCCTAA[C/T]ATTTAGATAGTCACA | 11124 |
rs537480865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626226 | AGTTGTTAAGAATTG[C/G]AAACTGAGTTTTAGA | 11124 |
rs537493138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820595 | TGCTGTACCTTAGAT[C/T]CTCAGAATTTATTCA | 11124 |
rs537494398 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50721213 | TCACTCTTATCACCA[C/T]GCTGGAGATAAGTCT | 11124 |
rs537497536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559124 | GGCATGGTGGCAAGC[A/G]CCTGTAGCCCCAGCT | 11124 |
rs537510921 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50659395 | GGGAAGGACACTGAT[C/T]GATTTGGGACTTGAG | 11124 |
rs537511789 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961395 | ATTGAAAGTTTCAAC[C/G]CATGGTCAGAAATTG | 11124 |
rs537523149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50615935 | ATCTTTGCCAAGGCC[C/T]TTATTGAGAAGGGTA | 11124 |
rs537523533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50768244 | ATTCAACAAGAAGAC[C/G]TAACTATCCTAAATA | 11124 |
rs537529483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912214 | ACAGAAAGCACAGGA[G/T]ACAGGAATGGTGTAT | 11124 |
rs537536834 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50845207 | AAAAGGCACTGGAAG[C/G]ACACTGCAGAAGGAA | 11124 |
rs537561992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50706294 | TCTAGAATAACAGAA[A/G]TATGAAACTATTATT | 11124 |
rs537574533 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50962147 | ACACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 11124 |
rs537574680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50952826 | GCGAGGAGCCCCTCC[A/G]CCCGGCAGCCGCCCC | 11124 |
rs537588156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760502 | CTCTCAGACCACGGT[A/G]CAATCAAACTAGAAC | 11124 |
rs537589575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50664059 | CTGGAGTGTAGTGAC[A/G]CGATCTTGGCTCACT | 11124 |
rs537591389 | in-del | -/TA | 0.00160032 | 0.0282418 | intron-variant | FAF1 | GRCh38.p7 | 1:50447194 | CAGGGGCACGATCTC[-/TA]GGCTCACTGCAAGCT | 11124 |
rs537596077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50660639 | GCTGGGATTACAGGA[A/G]TGTGCCACCACACCT | 11124 |
rs537599121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681761 | TGACCTCAGGTGATC[A/C]ACCTGCCCTGGCCTC | 11124 |
rs537600385 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50626384 | AATAAAATATAAAAT[C/T]ACAACTGTAAATGCA | 11124 |
rs537605682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50691484 | TGACCTCAAGTAATC[C/T]GCTGGCCTTGGCCTC | 11124 |
rs537622871 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50787041 | CATCTAGAATTCAGA[-/T]TTAAGGTAAACCACA | 11124 |
rs537623847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50648520 | CCTGGAAGGGAAGTT[G/T]CAGACTAAAGAATGA | 11124 |
rs537625242 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50671617 | CCTTTTTTTGGGTCA[A/G]GATCCTTAATGTATT | 11124 |
rs537642388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50837890 | CTGGGACTACAGGCG[C/T]GTGACACCATGCCCA | 11124 |
rs537650033 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50636722 | ATGAAGTCCAATTTA[C/T]CCATTTTTTTTCCTC | 11124 |
rs537668616 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50632752 | TCCAGCTCTCAAGGT[G/T]TCCCACACTTATGCA | 11124 |
rs537671002 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50783216 | TTATAGAGAGTGAAT[A/C]AGTAATCAAAAATCT | 11124 |
rs537676517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50478921 | CAAATCTTAAGTGTA[C/T]AACTTGATAAAGTTT | 11124 |
rs537682053 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50638331 | TGTACTAAGACTAGC[A/C]GTATAACATTGAATA | 11124 |
rs537693270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938996 | CTTTGAAGTTGGGTG[G/T]TATAATGCCTCCCAC | 11124 |
rs537704569 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50740469 | GTGCAGTCTTAATCC[A/G]AGGGTATTGAGACTT | 11124 |
rs537715141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50575260 | TAATTTAAGAAATAA[C/T]TTTAATATGGGCACT | 11124 |
rs537715796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50827093 | GGAGCGCCTCTGCCC[A/G]GCCACCCCATCTGGG | 11124 |
rs537720271 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50663712 | CCGGCCAGAAGCACC[A/G]CTTTAGAATGTGCAA | 11124 |
rs537726501 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881790 | CACAGAGGATTATAT[A/T]AAATGCCTATATATA | 11124 |
rs537737281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948516 | TCTCAGACTCTTATT[A/T]CTTTTTCTTTTCTTT | 11124 |
rs537737571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518255 | TTACAAAGCATAATG[C/T]CTTTGTGATACATTC | 11124 |
rs537752872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50784957 | TCAAAAAATGGTACT[A/G]GGAAAACTGGATATC | 11124 |
rs537759317 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50665996 | AGTCTGGCCAACATG[C/G]TGAAACCCTGTCTCC | 11124 |
rs537759612 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50633577 | AAGCAATCACAAAAG[A/G]GCTCTGTCTTGGCTT | 11124 |
rs537760538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931213 | CTATCTTGGTTCTCA[A/G]TTTACTATCTTGGTT | 11124 |
rs537766184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50923153 | GCTAAGTGCAATAAC[A/G]CACACCTATAATCTC | 11124 |
rs537774487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525678 | TGAGTACGATGTTGG[C/T]TGTGGGTTTTTCATA | 11124 |
rs537785521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50529211 | TCATCATTACTTTTA[C/T]GTTTCAATGAACCAT | 11124 |
rs537794556 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50708207 | ACAGTGAGCAAAGAC[G/T]GGGGGTAGGGAGAGC | 11124 |
rs537797426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525607 | AAGGCAGCAGGGAAG[G/T]TGGAATCCTTGCTTT | 11124 |
rs537798166 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50646079 | CCCATGTAATCTTCA[A/C]AATAGGTTTTCAAGT | 11124 |
rs537801580 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50831612 | GACCCCTACTAATAA[C/G]AGTTTTATCTAATTG | 11124 |
rs537801868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50702547 | TTAAGACTACTTGCA[A/T]CTCTCTCCATTCTGA | 11124 |
rs537803199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823239 | CAACCCTGAATATAG[C/G]TGCCTACATTTTGAG | 11124 |
rs537806879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927088 | GGAATGGGGAGTTAA[A/T]GTTTAGAAGCAGAAA | 11124 |
rs537808714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50686484 | GAGGTGGAAGTTGCC[A/G]TGAGCTGAGATTGCA | 11124 |
rs537809953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50589551 | ATTACTTAGTTTTAG[A/G]AGTTCTCTATATTTT | 11124 |
rs537823634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50531367 | CAATAAATAGATCAC[A/C]AACTAAGTATCACAA | 11124 |
rs537832615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944297 | GCTAAATTTAATGTG[A/G]TAACAACAATTTGGA | 11124 |
rs537845773 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50704019 | ATGCCACTACTTTAT[A/C]ATCACCGAACATTAA | 11124 |
rs537867308 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50491859 | TTTGAAAAAAAAGAG[-/A]AAAAAAAACTAATGG | 11124 |
rs537867373 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50945376 | AAAGGTCCAATGTAT[A/T]CAATCTGCCAGGAGC | 11124 |
rs537871481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50893837 | ACAGAAGCCAGACTA[A/G]GGTCAAACACCTTAG | 11124 |
rs537878804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618835 | CTCACTGCAGCATCT[A/G]CCTCCTGGGTTCCAG | 11124 |
rs537879010 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50794898 | CGCCTTGGCCTCCCA[A/T]AGTGCTGGGATTACA | 11124 |
rs537880946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927982 | TATACTGTTAGGATT[A/T]GTGTTCTTTGCTGAG | 11124 |
rs537884190 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50716234 | AACTGTCTTGAACCA[A/G]TAATAATCACAGTAA | 11124 |
rs537886407 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50527480 | GTCCTTTGAAGTAGT[C/T]AGTCAACAGTACTGA | 11124 |
rs537887621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841577 | AACCAAGCTTTTTTT[C/T]CCCTTTCTTTCTTTG | 11124 |
rs537888142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824157 | AAATATGCATGTATG[A/C]CTATTTTAACAAGCT | 11124 |
rs537894308 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50709082 | CTTTCAAAGGTAGAT[C/T]TATTGTACAACTATT | 11124 |
rs537896265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50716860 | CAGTGGCGACCCACT[C/T]GGGTCCCCTTCCACG | 11124 |
rs537911303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816443 | TCTCCTGACCTCGTG[A/G]TCCTTCCGCCTCGGC | 11124 |
rs537912208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728872 | GCTGTAGTTTTATGG[A/G]GAGGACTAGTTCATT | 11124 |
rs537913373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871555 | TCTATTCTGCCTGTG[C/T]TCTCTAAATGGAACA | 11124 |
rs537919599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50611453 | CACCTCTGAAAGACC[C/T]AGGATAGTTGGAGGT | 11124 |
rs537921611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50496999 | AAAGTTACTTTAAGA[A/C]ATAATCATTGAAATT | 11124 |
rs537942735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786945 | TTAAGAGTTTAACAG[C/G]TTTGCTTTCCAAGAC | 11124 |
rs537947013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687071 | TGACCTCAGGCCATC[C/T]GTCCACCTGAGCCTT | 11124 |
rs537950143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50863250 | GGAAATTAAATAATC[C/T]GCTCCTGAATGATCT | 11124 |
rs537955945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50709827 | GATAGAAATCACTGA[C/T]CTCAGAGAGGTTCGA | 11124 |
rs537966248 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50561687 | AAAAATTAGCCAGGC[A/G]TGGTGGCACACACCT | 11124 |
rs537969416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50928624 | CCATCTCTACTAAAA[A/C]TACAAAGTATCAGCC | 11124 |
rs537971187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50897625 | TGTTCACTATAAAGT[C/T]GACCTAAAAACATTT | 11124 |
rs537973954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50955978 | GGATGGTGGTTGCCA[A/G]GGGCTGAGGAGAGAG | 11124 |
rs537979558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833813 | GACCAGATATCTTTC[C/T]GTGATACCACATCTG | 11124 |
rs537985483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50680815 | TTCTGACAAATGGTC[A/G]GAATTTCGAGAGTTT | 11124 |
rs537991434 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50523077 | CAAGATTCATTTATG[C/T]TGCAACATTTATCAG | 11124 |
rs537993585 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50535957 | GACTAAGGTCAAGCT[G/T]GTTAAGTGGTGAGGC | 11124 |
rs538000363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50684632 | ATCCCACTGAAGCCA[A/G]TTTCAAGGTACCAAC | 11124 |
rs538003222 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50587311 | TAAAATTCCAGAAAA[A/C]AAAATCCTATAACCA | 11124 |
rs538012653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50537806 | ACTGGTTGAAATTTA[C/T]GAAGAAAATCTGGTC | 11124 |
rs538016694 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50875694 | TGATCTTGTGATCCA[-/C]CCCCCCTCGGCCTTC | 11124 |
rs538023316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912901 | ACCAAAACTGAATTC[C/T]GATAAACTATGTTTC | 11124 |
rs538023343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50906585 | AGTTCTCCTTGAAGA[G/T]GTCCTTCACGTCCCT | 11124 |
rs538033236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50656321 | TGGGCAACAGAGTGA[A/G]ACTCCATCTCCCTAC | 11124 |
rs538033647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469667 | AGTGGGGAGCATAGA[C/T]GTGGGGAGGCAAAAC | 11124 |
rs538038433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50863745 | GGAGGATTCCCTCTT[C/T]TTCTATTGATTGGAA | 11124 |
rs538047371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50537057 | CTCAGCCTTCCAAGT[A/G]GCTGGGATTATAGGT | 11124 |
rs538050272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50949920 | AGGCTGGTGTGCAGC[A/G]GTGCAATCATATCCT | 11124 |
rs538058805 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50874710 | AGTCAGAAATGTTTA[G/T]AGATGATTTAAGTCT | 11124 |
rs538063206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50891511 | TCTACCTTTGGTCTT[A/T]GATGATAGTGACATA | 11124 |
rs538066715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50899994 | ATAGTCTATGCTTTG[C/T]GTGAGTGCTAGAGAT | 11124 |
rs538067693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50792713 | GCATTTTAAAATACA[C/T]TAGTAAGGGAATCTG | 11124 |
rs538068666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50754930 | TATCATGAGAACAGC[A/G]TGGGAAAGACCCACC | 11124 |
rs538069963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649302 | GGATTACAGGCATGC[A/G]CCACACACCTGGCTA | 11124 |
rs538095894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461248 | AGTCTGCACCACTGA[G/T]AGAGGACTTTTTATT | 11124 |
rs538096982 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50809490 | GCTATGAACATCTCT[A/C/T]TATGCACAAAGGCTA | 11124 |
rs538101098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793690 | TTTCACACAGCAGGG[C/T]AGACTAATACCTTCA | 11124 |
rs538116531 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50910580 | CTACTCAAGCCTCAG[C/G]AATGGCGGACGCCCC | 11124 |
rs538137275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685093 | TCTTGAAACACATAC[A/G]GATCTTTGAATGGCA | 11124 |
rs538146652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50776043 | TATAATAACAATATC[G/T]GATTTAAAATTCATT | 11124 |
rs538147706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50702337 | AAATCTGAATTCTCA[A/G]CGTAAAAAAAATTCA | 11124 |
rs538157350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50490334 | TACAGTGAGCCCAGA[C/T]GGTGCCACTGCACTC | 11124 |
rs538165833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50794049 | CTGAAATGTGAAATA[C/T]TTCTGGTCCTATGCA | 11124 |
rs538176691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50678729 | AGGTTGCAGTGAACC[A/G]AGACTGTGCCACTGC | 11124 |
rs538193387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940533 | CCAAAGTGCTGGGAT[C/T]ATAGGCATGAGCCAA | 11124 |
rs538213484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50584567 | TGCCTACTCTCTATT[A/G]TCTTATCTCCTCAAA | 11124 |
rs538230827 | snp | A/G | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50745264 | CGAGATCGTGCCACT[A/G]CACTCCAGCCTGGGT | 11124 |
rs538231962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50472599 | GAAGTATTGTTTTGG[C/T]TGGGGGCGGGTGGCA | 11124 |
rs538239838 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50530712 | ATGATGTGCTTATTT[C/T]GCATTGCATGCCTGT | 11124 |
rs538246276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742115 | GGAATTCAGGATCAG[C/T]CTGGAAAACATAGCA | 11124 |
rs538246408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50733361 | ATTATTACACCTTTC[A/C]TACTGTCTCTAAACC | 11124 |
rs538253994 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50683249 | CATTATACCTCGGCC[A/G]GGTGTGGTGGCTCAC | 11124 |
rs538255757 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50844579 | AATCTAGAGTCTGAA[C/G]ACCTGGGCTTCGAGT | 11124 |
rs538259338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543522 | GTCTTCTTGTAAGGA[A/T]GAAATAAGTTAAGAT | 11124 |
rs538259616 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50523387 | CCCAATCAGCAATGT[A/G]CAAGGGTTCTAAATT | 11124 |
rs538262528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786170 | TCATGTTCATTGCAG[C/T]GTTATTCACAACAGC | 11124 |
rs538267156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50482139 | TCTCTCCCCGTTCAA[A/C]TTTCTTCATCCCTAG | 11124 |
rs538267920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534449 | CACCATACCCAGCTC[A/C]TTTTTGTATTTTTAG | 11124 |
rs538274544 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50832963 | GGAGTCCTTTTTTGC[A/T]GCGAAGACAGGATCT | 11124 |
rs538281650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931368 | TTAGTTTGTTTTCAC[A/G]CTGCTGATAAAGACA | 11124 |
rs538283725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836327 | TAGCATGAGTCACCA[C/T]GCCCAGCCATGTTTT | 11124 |
rs538287782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940192 | GCTGGGATTACAGGC[A/G]TCGAGCCACCATGCC | 11124 |
rs538290900 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50476859 | AAAGAAATAATTTAG[-/A]AAAAAAAGAAATATA | 11124 |
rs538292148 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50827832 | CGACAGAGAGCCTAA[A/C]AGAGTACTAAGAGAT | 11124 |
rs538295617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50881582 | TGATACAGAGGATAC[C/T]GGGGATTTGAGTAAA | 11124 |
rs538299830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888285 | TTTTGGGCTGAGACG[A/G]TGGGGTTTTCTAAAT | 11124 |
rs538303171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50725296 | TACAGTGATTCTGAA[A/G]CCAAGCTGGACCTAA | 11124 |
rs538305991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50734048 | GCAATCCACTCACCT[C/T]GGCCTCTCAAAGTGT | 11124 |
rs538312909 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50810999 | GCAGAGAGGTGAGAT[C/T]GTGCCACTGTTCCAG | 11124 |
rs538314692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576359 | TATGTATAATATTTG[G/T]AAAAAGCACTGGTGT | 11124 |
rs538319660 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50903674 | AAAGAAAAAATTCAA[C/T]TTGCTAACCAACCAC | 11124 |
rs538323269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728395 | GAGCCAGAGGGACAG[A/C]GATAAAAGACGAAGT | 11124 |
rs538325772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50777935 | AACATATATCTTCAC[A/G]CTATGATTCAGCAGC | 11124 |
rs538330395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516054 | ATTTAATCTTCACAA[C/T]AATCTTATCAAGTGG | 11124 |
rs538344617 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50769835 | GCAGGTGGATCACTT[A/G]GGGTCAGGAGTTTGA | 11124 |
rs538344991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682982 | AGGCTGCAGTGAGCC[A/G]AGATCACACCACTAC | 11124 |
rs538369376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50932138 | TGGGGACACAGCCAA[A/C]CATATCATTCCACCC | 11124 |
rs538369405 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50567703 | TAGTCTCTTCCATTT[A/G]AAAGGAAAAGGTCTG | 11124 |
rs538383513 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50888678 | GTTTACTGATTTGCG[-/T]TATGTCGAACGAGCC | 11124 |
rs538386575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585942 | CCGCTGGTCTTAGTT[A/G]CTTGGGAGGCTGAGG | 11124 |
rs538401260 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50776293 | GCTACAGACACATTA[C/T]AAATACAACTGGACT | 11124 |
rs538404600 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50848985 | TGTACTAAGCCAGGC[A/G]CAGTGGCTCATGCCT | 11124 |
rs538411091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808881 | AAACAAATCCAGCAG[C/T]ACATCCAGTAAGGGC | 11124 |
rs538418727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50916163 | AAACAAAAGGGGGTC[A/G]TAGGAGGAAGGGTAG | 11124 |
rs538432520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956730 | AAGGCAGGTGGATCA[A/C]CTGAGGTCGGGGGTT | 11124 |
rs538436009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50812311 | ACCTACAGAATGGGA[C/G]AAGATATACGTATCC | 11124 |
rs538437549 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50540057 | GCTCACTGAAACCCC[C/T]GCCTCCCGGGTTCAA | 11124 |
rs538456318 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FAF1 | GRCh38.p7 | 1:50441174 | CTTGAACAATGCATT[C/T]GTCATTGAAGGAGGG | 11124 |
rs538469184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847313 | ATGTTAGAACAGGAA[A/G]TTTTAGATGACTATG | 11124 |
rs538479480 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50606790 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCTGAGCT | 11124 |
rs538482677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705531 | TGAAATATATTACAT[A/G]ATAATCAGTTATTTT | 11124 |
rs538485855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50805197 | GGTGGATCATTATCA[C/T]ACTGTAATGTATTTT | 11124 |
rs538488116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50642713 | TTGTTTTTTAAAGTT[C/T]ATTTTTAATAATCTT | 11124 |
rs538489285 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50604061 | ACACAAACACTACCA[C/T]GTAAGCAACCGGAGC | 11124 |
rs538499954 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50796894 | CAACACTTTGGGAGG[C/T]CGAGGCAGGAGGATC | 11124 |
rs538501779 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50805841 | TTGTGGTAACAATAA[C/T]GGCAGCTAACACTGT | 11124 |
rs538511838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952782 | CTGGGAGGTGAGGAG[C/G]ATCTCTGCCCGGCCG | 11124 |
rs538514723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50692368 | TATAGTCACCCTGCT[A/G]TACGAAAGACCATTA | 11124 |
rs538522132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50493801 | CTCATCCACAAAATG[G/T]CTGGCCCAATCTGAG | 11124 |
rs538524843 | snp | C/T | 4.94988e-05 | 0.00497463 | missense | FAF1 | GRCh38.p7 | 1:50596137 | TCTTCCGACTGTTCC[C/T]GGGTCTGTGCAGGTG | 11124 |
rs538525596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50900827 | TTCACTTAGTAAATT[A/C]TATTTATGTGTGTGT | 11124 |
rs538532026 | in-del | -/AT | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684350 | ACTCAGTCTCAAAAA[-/AT]TCACTAGATTCTGAA | 11124 |
rs538542511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695624 | TATATATGATTTCTC[C/T]CTATAAGACAAAGTT | 11124 |
rs538547084 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50795129 | ACACCACAACATGGA[A/C]TGCCCCTCACCAAGG | 11124 |
rs538552037 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50590927 | GCGGAGGTTGCAGTG[A/T]GCCAAGATCGTGCCA | 11124 |
rs538556029 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50923242 | TGGGCAATATAGAAA[A/C]ACCCATCACTACAAA | 11124 |
rs538559131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50596931 | TAAACCTGTCTTTAA[A/G]AGATACTTTGAAAAA | 11124 |
rs538562018 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50639885 | GTTGCAGTGAGCCGA[A/T]ATCATGCCACTGCAC | 11124 |
rs538570155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688741 | CACTTGAACCCGGGA[G/T]GCGGAGGTTGCGGTG | 11124 |
rs538576665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50547350 | TCATCTGCCTGAGGC[G/T]TCCAGTAATAGTAAA | 11124 |
rs538576901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50591960 | CTAGTCTTTTTTTAT[C/T]TCCTTTATTTAAAAA | 11124 |
rs538593264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50550269 | GGCAGGAGAATGGCG[A/T]GAACCCAGGAGGCAG | 11124 |
rs538594642 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50528470 | AATGTTCTAAGAAAC[A/G]CTGACACTAGGGGTA | 11124 |
rs538595322 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869977 | AAGATTTATTTTCAT[A/G]CCATGCATTATGATG | 11124 |
rs538601214 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50595914 | TCTGAATTCCGTCTG[C/T]TGAAACATGAAACTA | 11124 |
rs538606353 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50473023 | TCTGTTCTCATTTGG[A/C]CCAGCCTCTGTTCAT | 11124 |
rs538606892 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50646419 | ATACTCATACAAATC[C/G]ATCCTTTAGTTGTTT | 11124 |
rs538621846 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50444670 | CTATCACTTATCGAG[A/T]GCCTACTATGTAGCT | 11124 |
rs538626711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50744444 | TTTAAAAGTTAGAAA[C/T]AGGAAAAACATGCCA | 11124 |
rs538628780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50476302 | AAAGTTTTAAAAAAT[A/G]GAAAGAACTTCAAAT | 11124 |
rs538631849 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50861569 | GCAGGGTAGGAGGTA[A/G]TAAGGGACAAAAATG | 11124 |
rs538636013 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50444578 | CTGCCGACGTGGCTA[C/T]TACTGCTTCTCTTAT | 11124 |
rs538649493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896889 | TGCACAATTTAACTA[C/T]ACTTAATACCACTGG | 11124 |
rs538656553 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50447820 | TTCAGTTATAGACTA[C/T]GTACTTCAGAAAACC | 11124 |
rs538659169 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FAF1 | GRCh38.p7 | 1:50889761 | CTGTTCTTTTACATT[G/T]GCTGAGGAGTGCTTT | 11124 |
rs538665447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50475276 | GCTACTGGGTACATA[G/T]CTGCTGGCCTGGGAA | 11124 |
rs538665827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50845204 | TGTAAAAGGCACTGG[A/T]AGGACACTGCAGAAG | 11124 |
rs538675986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50708079 | TCACAAAGTGCTGGG[G/T]TTACAGGTGTGAGCC | 11124 |
rs538681393 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50951249 | AAACGAACAAACAAA[C/T]AAAATTTGTTTCAAA | 11124 |
rs538685640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50494972 | TTACTTATTTTTAGT[C/T]AAAAAAATTTTTTTT | 11124 |
rs538692409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50601772 | CATATATATTCATAT[A/G]TATACATATATTCAT | 11124 |
rs538694996 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50771648 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 11124 |
rs538695632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50630713 | CCACAGTATTGAAAA[A/G]TGTATCATATAATAA | 11124 |
rs538697508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50639790 | AATACAAAAATTAGC[C/T]GGGCATGGTGGCATG | 11124 |
rs538699028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50504588 | TAAAGAGATCATGTT[C/T]TTGAATTTTCTAGTA | 11124 |
rs538713999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948570 | CAGAGTCTTGCTCTG[A/T]CGCCCAGGCTGGAGT | 11124 |
rs538718897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852465 | ACTGAGAATCTATTT[A/G]AAAACAAAGCAGAAA | 11124 |
rs538726273 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50699684 | ACTTCTAATTAGTTA[C/T]AATAATCTCTGCTTC | 11124 |
rs538729220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602332 | AATGCTACCGGATAT[C/T]AGCACTGACTACACT | 11124 |
rs538731481 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50483766 | CTGCATATATTTGCA[G/T]AGCCCACAGGATTTA | 11124 |
rs538735774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518904 | CGGCAGTGAATAATA[G/T]CTTTGGTTGTTCTCC | 11124 |
rs538737045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50781965 | CTATCATCTAGTGAC[A/G]TCTTAGCCACTGTAA | 11124 |
rs538739944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50772693 | AACAGACACTGGGGA[C/G]TACTTGAGAGTGGAG | 11124 |
rs538748964 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50528037 | TTGGCTAATTTTTTT[C/T]CCCTATTTTTTGTAG | 11124 |
rs538750507 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50897808 | CAAAACATGGTCAGA[A/T]GTCACATTGTGACAA | 11124 |
rs538758032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50700352 | CATTTGGAGTCGAAC[A/G]CAGCCCCCGGCCTTT | 11124 |
rs538761211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526454 | TAATAATAATATTTA[C/T]TATTTTTAAATAATT | 11124 |
rs538767500 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50478216 | TCGCCCAGGCTGGAG[C/T]GTGATGGCGCAATCT | 11124 |
rs538768107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846196 | ATTTGCCTTTGTCTA[C/T]ACTATGCTACATACG | 11124 |
rs538772900 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50746567 | TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 11124 |
rs538784435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50753435 | TGGAGCTATTACAAA[A/G]AAAGTTGCTATAAAC | 11124 |
rs538790661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50891005 | GGTACACCAATCAAA[C/T]GTAGATTTGGTCTTT | 11124 |
rs538806114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50828404 | CTCCCAAGCAGTTGG[A/G]ACTACAGGCGCCCGC | 11124 |
rs538810665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50867972 | GAAAGTGTGGTATAT[A/G]TATCCCATGGAATAC | 11124 |
rs538817613 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50924960 | TGCACTCCAGCCTGG[G/T]TGACAAGAATGAAAC | 11124 |
rs538819105 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50858695 | TCTTTTTACCCCTTT[A/C]ACATAAATACTAAGA | 11124 |
rs538824221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451470 | CTGCCTAAGAATGCA[C/T]AGGCAGGAAGTGGCA | 11124 |
rs538825068 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50738416 | CCATTGCACCTCAGT[C/G]TGGGCAACAAGAGTG | 11124 |
rs538828106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50668859 | AAAATTTAACCACAT[A/G]ATTCATTAAATAAGG | 11124 |
rs538829631 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961259 | TGGGCAAGCTGATCT[C/T]GAACTCCTGTCCTCG | 11124 |
rs538833628 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50686112 | TATGATAATGTAAAC[A/G]GTACCCAATAATAGT | 11124 |
rs538835258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50904131 | CAACCTAAATGTCCA[C/T]TGATAGATGAATAAA | 11124 |
rs538837815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50449993 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 11124 |
rs538841452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50757593 | ATTACAATTTTCATA[C/T]ATATTTTCCAGTTCT | 11124 |
rs538852866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50623438 | GCTGGGTGTGGCGGC[A/G]TGCACCTGTAGTCCC | 11124 |
rs538857034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50460121 | TCTGTTGGATTAATG[C/T]GTAGAAAACTCTTCC | 11124 |
rs538868401 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50633614 | GAGCTCTGTCACTAC[A/G]GCAACCAGCAGGGAA | 11124 |
rs538870705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50501429 | CAGCACTTTGGAAGG[C/T]CAAGGCAGGCGGATC | 11124 |
rs538876726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50567595 | GAAATATTAACTTTG[A/G]ACTGTTCAACAATAC | 11124 |
rs538880983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50877056 | TATGTAGCTACTCCA[C/T]CCTCAAGGAGGTTGA | 11124 |
rs538881752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607744 | TCCAAAACACTTGGT[A/T]TCTTTTGGTAGTCAA | 11124 |
rs538884323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721945 | CCTTTTCTGCTGCAC[G/T]GCTAAAACCTCACAA | 11124 |
rs538893807 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50479113 | GGGGTATGACAGACA[C/T]GCGTTCAAATCCTGG | 11124 |
rs538895580 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50644921 | CATGTGTTCTTCTTC[A/G]TATTTACTGAGCAAA | 11124 |
rs538897442 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50690506 | TTCGGGAGGCTGAGG[G/T]AGGAGAATCGCTTGA | 11124 |
rs538898447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714537 | AACAAAAAACCAAAA[C/G]AAACAAACAAAAAAA | 11124 |
rs538905668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50859633 | TAAAAAACATTCCAT[C/G]CTCACAGGTTGGAAG | 11124 |
rs538908771 | snp | C/T | 5.4759e-05 | 0.00523226 | intron-variant | FAF1 | GRCh38.p7 | 1:50452077 | TGGGGAGGAAAAAAC[C/T]GTCTTAGTCTAAAAA | 11124 |
rs538912286 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | FAF1 | GRCh38.p7 | 1:50917615 | AAAAGGAAAGGAAAA[A/G]GGAAAGGAAAAAGGA | 11124 |
rs538913702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50706101 | TTCTCTACCAAGGTG[A/T]TTTTAAATTTCAAGT | 11124 |
rs538917666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50608379 | ACCTCAATAGACAAA[A/G]GTTTTACATGAGTGG | 11124 |
rs538928149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50492956 | GCCTGAAGGTAATTG[C/T]TATACTACAAAATAT | 11124 |
rs538929350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50822201 | ATGTAACCATTCCAC[A/C]ATCTGTTTTTAGTCA | 11124 |
rs538929520 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50887718 | TTTTGGAGGGCTCTG[C/T]TCTGTTCCATTGGTC | 11124 |
rs538930483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50814248 | AATACTAGGTATAAT[A/G]TTAGCCTAATATTAT | 11124 |
rs538931479 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50881725 | TTATCACTGTTATCT[C/T]TCCCATTACATGAGT | 11124 |
rs538935069 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50842363 | TTTTAGCTTGCCATT[G/T]GAGGTCTATATTAAG | 11124 |
rs538941444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50851085 | GAGCAATTTACATTT[C/T]TTTTTTTTTTTTTTT | 11124 |
rs538948536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50696448 | GATTCTTTTTAATCA[A/G]CCCCAACAAACATTT | 11124 |
rs538951297 | in-del | -/A | | | intron-variant | FAF1 | GRCh38.p7 | 1:50786132 | TGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAT | 11124 |
rs538953978 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50609272 | CTTAGTAAGAATGAA[C/G]CTGGCATAGCTTGCC | 11124 |
rs538959864 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50744020 | AGTTTGCAGTGAGGC[A/G]AGATCATGCCACTAC | 11124 |
rs538960259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50715125 | ACCCTCAGATATAGA[C/T]TGAAGTTAATGTTCA | 11124 |
rs538972011 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50845468 | GTGGTTAGAGGGTTC[A/G]CACCAGGCTGCTGCT | 11124 |
rs538975165 | in-del | -/TATG | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50875323 | TATAATGTTTTGAAA[-/TATG]TATGTATACATTGTA | 11124 |
rs538975458 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50617769 | CTGGCAGAATTCAGC[C/T]GTGACTCCATCTGGT | 11124 |
rs538977971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707415 | AAAAATTAAGCATAA[G/T]GGGCTGGGTGCACTG | 11124 |
rs538985414 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50759153 | TTATTTTAATTTTTT[A/T]AAAATTATTATTATA | 11124 |
rs538992490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921117 | GTGTCCCCCAAAAAA[A/T]CAAACATACAATTAC | 11124 |
rs538994748 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50656755 | AGGTGTGGTGGTGTG[C/T]GCTTGTAATCCCAGC | 11124 |
rs539002608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50653849 | TACTCCAGACTGGGC[A/G]ATAGAGCAAGATTCC | 11124 |
rs539003533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50814954 | TGGTATCGCTGCTGT[C/T]GCAAACAATATGACA | 11124 |
rs539008787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50910637 | GTTCGATCTCAGACT[A/G]CTGTGCTAGCAGTGA | 11124 |
rs539010338 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50802551 | TAATCTCTGAGCTAA[A/C]AAGTTACCAAGTAGT | 11124 |
rs539012714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50758523 | AATTTCTACTTTTAA[A/G]TGTCAATTCTCATTT | 11124 |
rs539014847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806891 | CAAACAAACACATTC[A/C]AAGGATTAGCATTTT | 11124 |
rs539027495 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50707189 | GCCTGGGTGACACAG[A/C]GAGACTCTGTGTCAA | 11124 |
rs539033673 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50865071 | ACATTTATGCAGCCA[A/G]AAAACACATGAAAAA | 11124 |
rs539037814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50447724 | CTCTTACGCCAATGT[C/T]AAGGACAAGCAGGTC | 11124 |
rs539041708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50905717 | ATCCTTCACCCACTT[G/T]TTGATGGGGTTGATT | 11124 |
rs539044862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50551461 | AGGAATCTGTGTCCC[C/T]AAAAACATGTAAATA | 11124 |
rs539059814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50898827 | TTGATTTGATGCTTT[C/T]TAGTTTTCTTCATGT | 11124 |
rs539064932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50807387 | ACTTACAGTAATGCC[A/G]GTAGGGCGAAGGGGA | 11124 |
rs539065486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50447316 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 11124 |
rs539066896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50495075 | TACTTCATGGAAAGT[A/G]GGGTGTCCGTCCCCT | 11124 |
rs539077937 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50755540 | TGTCCGTGGATCTAC[A/C]ATTCTGGGGTCTGGA | 11124 |
rs539088106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50710989 | ATCTCGGCTCATTGC[A/G]ACCTCAACCTCCCAG | 11124 |
rs539091288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50799064 | TGATCTGCCAGCCTC[C/G]GCCTCCCAAAGTGCT | 11124 |
rs539107785 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50944099 | TACCCCACAGAATCT[G/T]AGTGAAGTTGATGAG | 11124 |
rs539111163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50482699 | TTTTCTTTTAAAAAG[C/T]CTTCTAAAAGGTGTA | 11124 |
rs539112285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50699110 | CATGGTGGCGGTAAT[A/T]TATGCCATCAAACAA | 11124 |
rs539121698 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50856728 | CTGAAAAAAATAGGT[A/T]AAATATGTAACATGT | 11124 |
rs539128214 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50703896 | TCAGGTGTGAGCAGA[C/T]TGCATTAACGCTGCT | 11124 |
rs539131309 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50906011 | GTTTTTATGGTTTTA[C/G]GTCTAACATTTGAGT | 11124 |
rs539139115 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50948960 | TAGGACCCACCTCCA[A/C]CTTTGGAGGTCACAT | 11124 |
rs539153779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50941271 | CTGGAGTGCAGTGGT[A/G]TGATCTCAGCTGACT | 11124 |
rs539158450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50857763 | ATAACTTAATACTGA[A/G]CTAAATATAAACTTC | 11124 |
rs539161759 | in-del | -/A | 0.245061 | 0.249951 | intron-variant | FAF1 | GRCh38.p7 | 1:50723399 | AGCAAGACTGTCTCC[-/A]AAAAAAAAAAAAAAA | 11124 |
rs539165715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50647818 | GATGAAGCCAGAGAG[A/G]AGGAAGGAAGGGAGA | 11124 |
rs539173325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952000 | TGACTTACCAGTATG[C/T]AACAGAAAAGTCCAT | 11124 |
rs539175729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598033 | GCGTGGTGGCTCATG[A/C]CTGTAATTCCAGCAC | 11124 |
rs539182383 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50676417 | TGTCTTAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 11124 |
rs539183700 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50880674 | TCTAGCCTCCAGAAC[C/T]GTGAGAAAATTTGTT | 11124 |
rs539184438 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50545163 | CTTACAAACTAGTAA[A/G]TAAAAGATCAACAAA | 11124 |
rs539186094 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50520863 | AAACCAAAAAACTTT[A/T]GCTCTTTATTAAAGT | 11124 |
rs539188751 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50512407 | AATCCACCTTGAGTT[A/C]ATTTTTGTATAAGGT | 11124 |
rs539189418 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50831252 | GATCCAGCAGCACTT[A/T]AGAACCTATGACTTC | 11124 |
rs539198431 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50729086 | TTGAGGCAGAGTTTC[C/G]CTATTGTTGCCCAGG | 11124 |
rs539204100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50832693 | TTACTGAAGGTTCTC[C/T]ACCTCTTTTCCCTGT | 11124 |
rs539207890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50679829 | ATCACTTCTGTACAT[A/G]CATTTACTTTAGTAC | 11124 |
rs539209180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50773703 | AGCTCCGTGGATAAA[A/G]AGAAAATATCAATCA | 11124 |
rs539209754 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | FAF1 | GRCh38.p7 | 1:50535650 | AGAAATAGTAGTATA[-/C]TGGCAGTTGAAATTT | 11124 |
rs539215657 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50511614 | AATATCCCGTGGTGT[A/G]TATGTGCCATATTTT | 11124 |
rs539217596 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50732266 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 11124 |
rs539223948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50724402 | AGATACCTATTACCA[C/T]TGCTGCTGGATGGTT | 11124 |
rs539236053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50458907 | AGATCAAACACCTAG[A/G]AAATGGTAAAAATGA | 11124 |
rs539268318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925433 | AAAGAACTAACAACC[A/G]GAATATACAAGGAAT | 11124 |
rs539278265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50560178 | ATGAACCACTGAGTA[A/G]TTTGGAATTAAGGGT | 11124 |
rs539280946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50581021 | CTCAAGTGATCCACT[C/T]GCCGTGGCTTCCCAA | 11124 |
rs539282752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463174 | GCACCCAATAAAAGC[C/T]CTGGGCAGAGTCCCT | 11124 |
rs539291596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50627053 | GAATAATATGAATTC[A/G]ATTTTGGATATGGTA | 11124 |
rs539294014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50617148 | CTTTCTCTTGCCTGA[C/T]TGCTGTGGCTAGGAC | 11124 |
rs539299905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50503608 | CAACAGAGTGATTCC[C/T]TGTCTCTTTAAAAAA | 11124 |
rs539300953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50717914 | TTAACCATAAAAAAA[A/T]GCCTGAATAATCGAA | 11124 |
rs539306286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50918274 | GTATACATGTGCCAT[A/G]CTGGTGTGCTGCACC | 11124 |
rs539310290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669860 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 11124 |
rs539313888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50882121 | AAATACATAAAATAT[A/G]TAATACACATAAAAA | 11124 |
rs539317442 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50725353 | CTCAATTTCTTCCAC[A/G]GCACCCACTGGAAAA | 11124 |
rs539325358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50765862 | TTGGAAGGCTGAGGC[A/G]GGTGGATGACCTGAG | 11124 |
rs539328071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620306 | AGTTGATTTGAAGAA[A/C]CAGTCTTTGAGCTCT | 11124 |
rs539335776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50825587 | AGGGGAGATTTTAAC[A/G]TATATCTACCAGTAA | 11124 |
rs539341195 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50556933 | GCAACTGACACATTT[C/T]AATGTGTACAAGTCT | 11124 |
rs539341342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50672626 | AGCTAGTAGTGACCC[C/T]ATTGGACAATATATT | 11124 |
rs539356852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512971 | GTAATCACACTCTAA[C/G]TGCAGAAAGTGGGGA | 11124 |
rs539357805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50690281 | GTGAGCCACCGCACC[C/T]GGCAAATTACATTAT | 11124 |
rs539358410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612706 | TGCTGGGCATCTTGT[C/T]CTGGCTTTTCCTCCT | 11124 |
rs539363463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870143 | ACACTCTACAGCACC[A/G]TGAAGATATTGCATT | 11124 |
rs539393602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50863901 | TTATTGGTCTATTCA[A/G]AGAGTCAACTTCTTC | 11124 |
rs539396846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50873223 | TAATGGGCTACATAA[C/T]AGTGTAAATATAACT | 11124 |
rs539402150 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50555921 | ACATATATATATATA[A/T]AATTAGGTGTGTGTA | 11124 |
rs539402916 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50674250 | GCCATTGCTCCGGGC[C/G]CCAAGGCAATTTTTT | 11124 |
rs539407740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50517653 | ATTTTGAGAACTCCC[A/G]CACCAATGGCTGCAG | 11124 |
rs539420695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50809856 | ATTGATGAACACAGA[C/T]GCAAATATCCTTGAC | 11124 |
rs539421547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779886 | CAGGGAATTCAAGAC[C/T]AGCCTGGGCCGCTTA | 11124 |
rs539422012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50771402 | ATATCCAGAATCTAT[A/G]AGAAACTTAAATTAA | 11124 |
rs539422509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650141 | AATACAAAATTAGCC[A/G]GGCGTGGTGGTGCAT | 11124 |
rs539423980 | in-del | -/TTGCTGGGCTTTTGCCC | 0.0158469 | 0.0875917 | intron-variant | FAF1 | GRCh38.p7 | 1:50638744 | CACCACGCCCAGCCT[-/TTGCTGGGCTTTTGCCC]AGCTATTGCTTTTTC | 11124 |
rs539427085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50547634 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 11124 |
rs539427280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50726656 | AACACAGTGAAACCC[A/G]GTCTCTACTAAAAAT | 11124 |
rs539431562 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50550519 | AGCACTTATTAAGCT[C/G]AATTCAGACAGCTGA | 11124 |
rs539436955 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50632318 | ATAAGACTGAAAGGT[C/T]AGAAACGAGTAACAC | 11124 |
rs539438953 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50591859 | CATGCTTTTTTTCTC[C/T]GAATGGAATGAATGG | 11124 |
rs539443990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50565706 | ACACTGCAATTTTTT[A/G]TCATTGTAAAATAAA | 11124 |
rs539445395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50657953 | GCAATATTTTGTTTA[C/T]AGTCAGTCACATCAT | 11124 |
rs539459749 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50907691 | TATAGTATTCTCTGA[G/T]GGTAGTTTGCATTTC | 11124 |
rs539461167 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50667141 | CACACATCTGAGAAA[C/G]ATGGCAAGATAAAAA | 11124 |
rs539464888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50883850 | GGAAATTAGGCCAGG[C/T]GCAGTGGCTCATACC | 11124 |
rs539483830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50810684 | ACCTAGAAAACCTCA[C/T]AGTTTCTGTCCAAAA | 11124 |
rs539486581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50621955 | CGGATGGCCTGAGGT[C/T]GGAAGTTCGAGACCA | 11124 |
rs539491550 | in-del | -/AAAC | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50607002 | AAATAACAACAACAA[-/AAAC]AAACAAACAAACAAA | 11124 |
rs539507170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50875280 | ATATATTTTAATTAA[A/C]AAAAATTGAATATAT | 11124 |
rs539517076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50908278 | ACATTTGCTGAGGAG[C/T]GCTTTACTTCCAACT | 11124 |
rs539523274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614579 | GCACGGTAGCTCACA[C/G]CTGTAATCCCAGCAC | 11124 |
rs539526549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50848717 | AAGAATGCATAAACT[A/C]ACTCTCTCATGAAAA | 11124 |
rs539527480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50510938 | TTACTTTATTTTAAA[A/C]TCTGCCTATGTATTA | 11124 |
rs539528469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50500423 | GAAAAAGGAAAACCT[C/T]TTAAACAAATAGCAC | 11124 |
rs539539057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50666670 | GGCGGATCACCTGAG[A/G]TCAGAAGTTTGAGAC | 11124 |
rs539541671 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50921812 | AAAGTATAAAATTCA[C/T]TGGTAGAGAGCAGAC | 11124 |
rs539548500 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50629239 | CAATGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 11124 |
rs539553356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50944538 | TTACTCACAACACCC[A/C]GACCTTTCATCTGGA | 11124 |
rs539554332 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50949777 | TGTCCTCAGTCCCAC[A/C/G]GCTGCCAAGTGATTC | 11124 |
rs539561139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50803717 | GATGGGGAGGGGATT[A/C]TATACAGAAGGAACA | 11124 |
rs539562674 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50800437 | AGTTCATCTGGTTTG[C/T]TTTCTAGACAAGGGC | 11124 |
rs539573712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50659253 | AGAAAGAGGGAGGGG[A/G]AAGGGAAAGGGAGAA | 11124 |
rs539575535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50667568 | TGTAAAACAGTGCCA[C/T]TAATCTACTCTGCCC | 11124 |
rs539582213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50927879 | GTGCCCTAATCTCCT[C/T]TTTTTCTTTTTTCTA | 11124 |
rs539585788 | in-del | -/ACTTTTAA | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50807465 | GGGGAAGTGCCACAC[-/ACTTTTAA]ACTATCAGATCTCAT | 11124 |
rs539589540 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50755413 | AAGAGGTGGCCTCCC[A/C]TGGCCTTGGGCAGCT | 11124 |
rs539601621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50590566 | CTTTGGAGTTGTCTA[C/T]ATATAAAATTATCCT | 11124 |
rs539602663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50694087 | CATGACATATATATA[A/T]AAAAAACTGACCAGC | 11124 |
rs539605062 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50732219 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 11124 |
rs539611358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50894120 | CCTGGCCAACATGGT[A/G]AAACTCCGTCTCTAC | 11124 |
rs539611821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902958 | TCACAGCTATCCAAC[C/T]ACACAATTTGGGTGT | 11124 |
rs539614666 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50472538 | TCAGGGAATTATGCT[C/T]AGCAGACATTTAGTA | 11124 |
rs539620885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50626605 | GACTACTTTGCAGAA[A/G]TAAGCAAGAATCAGA | 11124 |
rs539623989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644101 | TTTTCCTGCTTGTTC[A/G]TATGTGCAGTAACTT | 11124 |
rs539635066 | in-del | -/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50625014 | TCAAGAGATTCTCCT[-/G]CCTCAGCCTCCCGAG | 11124 |
rs539637521 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50749758 | GTTGCCACTGCACTC[G/T]ATCCTGGATGACAGA | 11124 |
rs539640591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50881533 | CTACCAAAAGAAGGA[A/G]CATCCAGTCTACAAT | 11124 |
rs539649149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894909 | TCAAGAGGGAAGTTT[A/C]TAGGTGTAAGCACCT | 11124 |
rs539651028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50742627 | GGCCTCAAGTGATCT[A/G]CCTGACTCAGCTTCC | 11124 |
rs539652433 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50572330 | TCTTGAGAATAATAC[A/G]TTCCCTTACATAATC | 11124 |
rs539658668 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467896 | GATTTACTCTTTCTA[-/C]AATGAATACATATAT | 11124 |
rs539664299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50824786 | AGAGAATGAAATCAT[C/G]TCATTTGAAGCAACA | 11124 |
rs539667173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50636915 | TTTACTGATATCCAG[C/T]TGCCTCATCGCCATT | 11124 |
rs539678079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50872538 | CATAACCTTAACTGA[A/T]AAAGCAGCAGTAGGG | 11124 |
rs539683780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50446732 | CTTTTATTTTGAAAT[A/T]GAATAAAAGAAAGTC | 11124 |
rs539691644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50483803 | AAATATGGATGTAAA[C/T]GAGATAAGTCAAGGA | 11124 |
rs539694180 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50768113 | GAAAAATCTACCAAG[G/T]CAACAGAAAACAGAA | 11124 |
rs539705734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50637532 | CCATACAATTTTTGG[A/C]ATTAATTTGCCAATT | 11124 |
rs539705773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50628168 | CTTGCCATGTTTAAA[A/T]GTGAACAGAATTTCT | 11124 |
rs539712826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734745 | TCTCAAAAAAAAAAA[A/G]AAAGAAAAAGAAAAA | 11124 |
rs539716119 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50650347 | GCACAGTGGCTTAGG[C/T]TTGTAATCCCAGCAC | 11124 |
rs539727951 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50517154 | CAAATTTTTTAAAAG[A/G]AAAATGCTATTTAAA | 11124 |
rs539728612 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50484103 | GTCAATATAATAGTC[A/G]TAATACTGGATGAGA | 11124 |
rs539729871 | snp | A/G | | | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50469493 | TGAGGAGGTAATCAG[A/G]AGAAGTGAGAAAAGG | 11124 |
rs539734708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50516858 | AAACACTTTGGATTG[A/G]TTGCAAAGTTGAATC | 11124 |
rs539734806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50710653 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGTGCGAC | 11124 |
rs539738418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888792 | TGAGGATTTTTGCAT[C/T]GATGTTCATCAGGGA | 11124 |
rs539750078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50815905 | GGTGGTGCATGCCTG[C/T]AGCCCCAGCTACTCT | 11124 |
rs539752863 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50618340 | TTTTGGTAATTTTCG[C/T]TAATACTGGTGTTCA | 11124 |
rs539754861 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50484778 | TGGATAGAAGCTCTG[G/T]TTCTGCTTTTATCAG | 11124 |
rs539758759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681598 | CTGAAACCTCTGCCC[C/G]CCGAGTTCAAATGAT | 11124 |
rs539762084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515954 | TCCAAACTTAGTTTA[C/T]ATTATTAGTATTACT | 11124 |
rs539767890 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50761054 | ATCAGAGAATACTAC[A/G]AACACCTCTGTGCAA | 11124 |
rs539774571 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50664792 | GAGCGAGACTCCGTC[A/T]CAAATAAACAAACAA | 11124 |
rs539774781 | snp | A/G | 0.359364 | 0.22481 | intron-variant | FAF1 | GRCh38.p7 | 1:50889280 | ATTAGTCTTGCTAGC[A/G]GTCTATCAATTTTGC | 11124 |
rs539781195 | in-del | -/ATTT | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50659918 | ATTAATATGGTACTG[-/ATTT]GTTTCCTTATTTGTC | 11124 |
rs539791304 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50751303 | AGAGCAGTGCTAGGG[C/G]CATTCAGCACTATTC | 11124 |
rs539791362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462611 | AGGCTCAAGGACAAC[C/T]GTAGGGGTTCGGAGC | 11124 |
rs539792583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50770409 | CAACTCCAGCAATGT[C/T]TCAGGATACAAAATC | 11124 |
rs539800534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513164 | AGCAATGACTTAGAA[A/G]GCCTCATCTATGTGA | 11124 |
rs539800837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50835376 | TATGTACATTGTAAA[C/G]AATGCAGACTTTAGA | 11124 |
rs539802260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50826730 | TGAACTTTATGCCAA[C/T]AAATATGAAAATTTA | 11124 |
rs539822135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714079 | CCTGGCCTGATATAC[A/G]AACTTTTTAAAAGCA | 11124 |
rs539824836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50819545 | GGCAGAAGGATCACT[G/T]GAGCCCAGGAGTTCG | 11124 |
rs539826266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50497709 | GCATGCCACCATGCC[C/T]GGCTAATATTTTGTA | 11124 |
rs539836862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50575164 | CCACCCGCCTCGGCC[A/T]CCCAAAGTGCTGGGA | 11124 |
rs539839578 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50883811 | AATTATTAATTTACT[C/G]AGACGTACAGTATTG | 11124 |
rs539840393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457056 | TCATCTAGAAAATAG[G/T]TTTTTTTCCCCTAGT | 11124 |
rs539841288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874669 | CAGCCAACTGCCCTA[C/T]ATATTTCAAACCCAC | 11124 |
rs539842727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50560347 | ACAAGTACCTGTCAG[C/G]ACAGCAGCGGAAGTT | 11124 |
rs539845083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50624163 | CTTTCGAACTTTTTT[C/T]TTCAGATGCAGTCTA | 11124 |
rs539848094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50814449 | CAATAAAATAAAAAA[C/G]AAACCGACTACAGAT | 11124 |
rs539861390 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50767442 | TAGACATGCCAACAT[C/T]CAAATATAAGAAATG | 11124 |
rs539868541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50918654 | GCCGCAATAAACATA[C/T]GTGTGCATGTGTCTT | 11124 |
rs539870185 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50938605 | ACTTGTCAATTTTTG[C/T]TTTGGTTGCAATTAC | 11124 |
rs539879849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50569173 | ATAAGGCTCAAAACA[A/C]ATGCCTCTATGAAAC | 11124 |
rs539885496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50827082 | CTGGGAGGTGAGGAG[C/T]GCCTCTGCCCGGCCA | 11124 |
rs539889485 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50512232 | TGCTGTGCAAGAAGC[G/T]CTTCAGTTTAATTAG | 11124 |
rs539890751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50521111 | ACTATATATACATTG[C/T]AGAATGGCTATATTG | 11124 |
rs539895226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50720519 | ACGGATAAATATTGA[C/T]GGAGTTCAGGAAATG | 11124 |
rs539895531 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50490668 | CGTGAGCTTCCCTCT[A/G]TTGATAAAACAGAAA | 11124 |
rs539912258 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50675167 | AGCACTGGGATTACA[G/T]GCGTGAGCCACAGCG | 11124 |
rs539931961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50615068 | GTAGTCCACAGTGTC[C/T]ACTGTTCCCATGTTT | 11124 |
rs539947148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50606935 | CCATTCAATTCCTGC[A/G]AGAGGAACTAAACCA | 11124 |
rs539947887 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50587602 | TAAATCCAGAAAAAG[C/T]ATTTATTCATAATTT | 11124 |
rs539952565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50698493 | TTCTGCTAACTGAGG[C/T]TCTGCCTTTAAAGAT | 11124 |
rs539953048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50712698 | TGTGTAATTTGCAAA[C/G]ACATTTTTGCTAAAA | 11124 |
rs539954782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910789 | GTCTGTCACAGCTTC[C/T]CTTGGCTAGGAAAGG | 11124 |
rs539969583 | snp | A/G | 0.0240643 | 0.107019 | utr-variant-5-prime, upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50959945 | GCGAGCCGGCGGGCG[A/G]GTCGGCGGGCCAGCG | 11124 |
rs539970605 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50503867 | AAAGTTCAGTGGATA[A/T]GTGGGACTTGGCTTG | 11124 |
rs539972322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50910244 | ATCCTTCCTCTGGAA[C/G]CTTTGTCTCAGAGGG | 11124 |
rs539985962 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50944917 | CCATTCTGATCATTA[C/T]TCAGGAGTGATCAAG | 11124 |
rs539998034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50852249 | CGCTCTTTCCTCAAA[C/T]CTTATGTTTGCCAGA | 11124 |
rs540000290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50759488 | ACATGAACTCATCAT[A/T]TTTTATGGCTGCATA | 11124 |
rs540008791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50526801 | ACATTCCCACTAGCA[A/G]CCAATGAGGGTTCAG | 11124 |
rs540009056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518598 | GGTGCCTCCCACCAC[A/G]TCTGGCTAATTTTTT | 11124 |
rs540017832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50841740 | ATTGTAAAAAATAAA[A/G]AGCCAGATAGTAAAA | 11124 |
rs540020635 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50876565 | TGAACTCCCAATGGC[C/T]AAAGCTAAAACATTT | 11124 |
rs540029826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50734210 | TGACTTCTCCCTCAA[C/T]TTCTCCTTCCTTCAC | 11124 |
rs540031996 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50445455 | ACATTACATTTTCAG[A/C]GATATTGCTGAGAGT | 11124 |
rs540039460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50644929 | CTTCTTCATATTTAC[C/T]GAGCAAACATTTCCC | 11124 |
rs540039934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50630180 | ATAATACAGAAGTCA[A/G]GAGAATGGTTACAGT | 11124 |
rs540041116 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | FAF1 | GRCh38.p7 | 1:50793847 | TGCATAAGCAGCAAG[G/T]ATAGGTTAAGTCTCC | 11124 |
rs540042995 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | FAF1 | GRCh38.p7 | 1:50890361 | ATTTAGCCCATTTAC[A/T]TTTAAGGTTAATATT | 11124 |
rs540044908 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | FAF1 | GRCh38.p7 | 1:50540870 | TGGAAATTCTGGGGA[C/T]TAGCCACTGGTACTG | 11124 |
rs540059807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50787117 | TAATCTGAATCAAAT[A/G]TAAGTTCAACATAGT | 11124 |
rs540076071 | snp | C/T | 0 | 0 | intron-variant | FAF1 | GRCh38.p7 | 1:50694698 | CGCCTGCAATCTCAG[C/T]ACTTTGGGAGGCCGA | 11124 |
rs540097049 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50685461 | GGATGAAAGATTTAG[C/G]AAATGGAATCAGAGA | 11124 |
rs540098079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50576025 | TACTAATTTTTGTGG[C/T]AGAAATGTTCATGGG | 11124 |
rs540098218 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50662802 | GCCTCCCGGGTTCAC[A/G]TCATTCTCCTGCCTC | 11124 |
rs540103041 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50681053 | ATAATAATAATACGA[C/G/T]GATGATGATTTGAGA | 11124 |
rs540122448 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50524313 | TGTACAGTTTGCAAA[A/C]ATTTTCTCCCATTCT | 11124 |
rs540132108 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50860511 | AAATGTTCCACATCA[A/C]CAATCACAGAGAAAT | 11124 |
rs540135779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50773305 | TTTAAAAATGTGACA[C/T]CAGATCCAGCCATCC | 11124 |
rs540138422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50938299 | CAGGAGGGAGCTCCT[C/T]GCCACTACCTTCATA | 11124 |
rs540147953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50774320 | TTTATTACTCATAAA[G/T]CATGGCTGAGGCATG | 11124 |
rs540154182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50669223 | GTTTCTCTAATCTCA[A/G]CTCTGAACTATGTCA | 11124 |
rs540156040 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50840169 | TTTCTAGAAGAAAAC[A/G]TAGGAAAAAATCTTT | 11124 |
rs540158929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50533555 | CTTGCTCTCAGTTTA[A/G]TGTAATACAGCGATA | 11124 |
rs540169409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50468383 | CTGCAACCTCCGCCT[C/T]CCAGGTTCAAGCAAT | 11124 |
rs540170136 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50866186 | AGCAAAATCAGCATA[A/G]AAAGGACATACCTTA | 11124 |
rs540183149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50821778 | ATGAACTGCTTTTAC[A/G]GTAATTATTGTCATA | 11124 |
rs540209188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50690805 | AGACTTGCCTACTCT[C/T]GGCATTTGATATAAA | 11124 |
rs540214722 | in-del | -/A | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50453203 | TCATTTAAACTTCTG[-/A]AAAAAATCTTTTCTC | 11124 |
rs540219305 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50904230 | TACAGTGTGGATGCA[C/T]CCTGAAGACATTAAT | 11124 |
rs540227093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50838821 | ATAACTCTTTCAAAA[C/T]TGTAACAATAAAAGT | 11124 |
rs540232815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723020 | GTATTAAGGAAGGAC[A/G]CCAAAGACTGAAATA | 11124 |
rs540233197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50886676 | GAATGATGGTTTCCA[C/G]CTTCATCCATGTCCC | 11124 |
rs540255648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50559715 | AATGAGTGGGTAGGA[C/T]GTAATCATGGAACAG | 11124 |
rs540259232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50451616 | AGGACTGTACCCTTC[A/G]TGTAACTGAAATGCA | 11124 |
rs540259940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739468 | CATACACATATATAA[A/G]ATGAACTAGCATAAA | 11124 |
rs540261554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50714807 | TCTAATAACTCTAAG[C/T]TCTGTCTATTTTCCA | 11124 |
rs540273192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50707637 | AGGTGGAGGTTGCAG[C/T]GAGCTGAGATGGCAC | 11124 |
rs540274314 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50578403 | TTCATTCAAAAATTT[A/T]AAAAAATAATCTTGA | 11124 |
rs540275699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528685 | ACAAGGGTCTGAACT[G/T]TGTAAGTCCACTTAC | 11124 |
rs540279457 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50650199 | TGAGGCAGGAGAATC[A/G]TTTGAATCCGGAAAG | 11124 |
rs540280424 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50723348 | GAGGTTGCAGTGAGC[A/G]GAGACTGTGCCACTG | 11124 |
rs540288695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50861189 | GGTAATAAACTTCTA[C/T]CTGTACTCCCTGAAT | 11124 |
rs540293998 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50723792 | TCGCTCAGGTTGCCC[A/C]AGCTGGAGTGTAATG | 11124 |
rs540302998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50609454 | CAGTGGCTTGATCAC[A/G]GCTCACCACAGCCTT | 11124 |
rs540304386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462569 | TGAAGAAAGTATTCT[C/T]CCTAGGCAGTGTGGG | 11124 |
rs540306773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685306 | TCACCTACATTGTCT[C/T]ACTTTCATTCTCACA | 11124 |
rs540318256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50949829 | CCTAGTCCAGTCTTC[G/T]GCTTACAGGTACATA | 11124 |
rs540332179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50602048 | AGATCCCTTCTAGCC[C/G]TAATGGGCTATGATC | 11124 |
rs540336928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50579403 | CATTTTCTGGTTACT[C/T]CAACTACTGGTAAGC | 11124 |
rs540337507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50571629 | CAATAGTGTCTGGGA[C/T]GCTTATTGTGTCTCT | 11124 |
rs540340854 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50461505 | GACCTGTGTAAGTAC[G/T]GTGCCAGAAACTGAG | 11124 |
rs540347393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50678869 | AGGCAGGCGGATCAC[A/G]AGGTCAGGATGATTG | 11124 |
rs540347890 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554645 | AATCACTCTGATCAG[A/T]TTATTACAAACTGGA | 11124 |
rs540352773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50654096 | AGCATCTACATAAAT[C/T]GTCTTAAAACTTTTC | 11124 |
rs540366180 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50687547 | CTGATGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 11124 |
rs540377938 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50861942 | AATCAGCTTTCAGAA[C/G]TACAAGGAGATAAAT | 11124 |
rs540383081 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50642274 | CCCAAATTTCTTATG[-/T]TTAGTGTTTGGATGG | 11124 |
rs540383979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585477 | TTTTCAGCAACATCA[A/G]TTGAAAAGGTATTAA | 11124 |
rs540404041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50940464 | GATGAGGTCTCAATA[C/T]GTCGTCTAAGCTGTT | 11124 |
rs540408945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50545461 | TTTAGTAGAGATGGG[A/G]TTGCACCATGTTGGC | 11124 |
rs540409283 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50807573 | CTCCCCCAACATTGG[A/G]AATTACAATTCAACA | 11124 |
rs540414145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736854 | ATTACCATCAACTTT[G/T]AAGGTTCTGCATGGA | 11124 |
rs540417037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50948644 | TTCAAGCGATTCTCA[C/T]GCCTCAGCCTCCCAA | 11124 |
rs540421778 | in-del | -/T | 0.367913 | 0.220446 | intron-variant | FAF1 | GRCh38.p7 | 1:50618414 | GTGTAGTTTTTAGAG[-/T]TTTTTTTTTTTTTTT | 11124 |
rs540424511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50836587 | GAAAAGTACAATGAA[C/T]ATCAATGTACCTTTC | 11124 |
rs540429131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50685380 | TACTGATAAAGAGTC[C/T]GTGTAGCGAGATAGA | 11124 |
rs540430362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50728608 | CCAGCCTAGCCAACA[C/T]AGTGAAACCCTGCCT | 11124 |
rs540437031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50655032 | CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACT | 11124 |
rs540445860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50631180 | TATCCTGTTCCATTG[C/T]TATGAAATGGAACTC | 11124 |
rs540446913 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50474237 | GCCTTCAAGTAGCTG[A/C]AGACAACAATCACAT | 11124 |
rs540449429 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50798742 | ACTTATCCTATCTAC[C/T]TGTAAAATGAGGAAG | 11124 |
rs540450317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50544782 | ATAGAGTGGTCAGGG[A/G]AAGTCTCAATGAAAC | 11124 |
rs540452834 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50819923 | AAATATAAATAAATA[-/T]TTTTCCACTTTAATT | 11124 |
rs540459056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50683137 | CAATAGATGTTACAT[A/T]GGATGGTTAGAAAAA | 11124 |
rs540463969 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50592491 | AAAATATTAAATGAT[C/T]GTAAAGAAACTGTGT | 11124 |
rs540479778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50623520 | GGCAAGTTGCAGTGA[A/G]CTGAGATCGTGCCAC | 11124 |
rs540485864 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50657416 | ATGTTAAGACTTGAG[A/G]CCAGGCATGGTGTCT | 11124 |
rs540496133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50676429 | AAAAAAAGAAAGAAA[C/G]AAAATGAAACTAATT | 11124 |
rs540498878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50721465 | GGATCCGCCTGCGTC[A/G]GCCTCCCAAAGTGCT | 11124 |
rs540505331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459298 | GTCTTTTAACTACTA[C/T]CCAATAAAGTCTCTC | 11124 |
rs540507505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50586670 | TAGTTTGTTCGTAGA[C/T]CTAAGATCTCCTGGT | 11124 |
rs540514083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512674 | CAGGTAGTATAATGC[C/T]TCCAGCTCTGTTCTT | 11124 |
rs540532181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50837995 | TGATCGGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 11124 |
rs540538526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50942291 | AGATCGCTTGAGCCC[A/G]GGAGTTTGAGACCAG | 11124 |
rs540542562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50587651 | TAGTGATTATGCTTA[C/T]TGCATTCATTTATTA | 11124 |
rs540544824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50925078 | ATATTTTTAGCCAAC[G/T]GATACTCAGCAAAAG | 11124 |
rs540549478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50898985 | CAGATTCCAATTACA[C/T]GTTTTTTAGACTGCT | 11124 |
rs540549795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50594665 | ATCACGAGGTCAGGA[A/G]TTCGAGACCAGCCTG | 11124 |
rs540555145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50877501 | AAAAGAACATTAGGT[A/T]AAAATATCATATATT | 11124 |
rs540577397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50582483 | TGCACAATGATGACA[C/T]ACAAATTCGTGAAGA | 11124 |
rs540579817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50933463 | TCCAGTTGCCAACAA[A/G]TTCCTCATCTCCATC | 11124 |
rs540615338 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50730376 | CCCTTTTTTTCATAC[C/G]TAGTATTTTGTTTAT | 11124 |
rs540615491 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50584426 | TAAAGAGAGACAGTC[A/G]TAATTCATTATACAT | 11124 |
rs540615904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842755 | CCTACCTGACTCTAC[A/G]ATATAAAATAACCCC | 11124 |
rs540617101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50632922 | GAACTGCTTTCCTTC[G/T]CAGTGTTCTTCTCCA | 11124 |
rs540628151 | snp | C/T | | | intron-variant, downstream-variant-500B | FAF1, LOC105378715 | GRCh38.p7 | 1:50471564 | CCTCATTACTTTGTT[C/T]TAGATATAAAATATA | 11124 |
rs540650904 | snp | A/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50463744 | GCTGGAAAAGGCTGT[A/T]AAAACTGAAGAGGTC | 11124 |
rs540655733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50834740 | GGATTAGAAGGAGGT[C/T]CACTAATCTCCATTC | 11124 |
rs540658141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50926827 | ATCCACCCATGTTCA[C/T]AGTACCATTGTTGAC | 11124 |
rs540660878 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50734506 | TTGGGAAGCCGAGGC[A/G]GGTGGATCACGAGGT | 11124 |
rs540664678 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50905517 | CAGTGTAAAAGTATT[C/T]CTATTTCTCCACATC | 11124 |
rs540665650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50775577 | GAAAAGGTTTATCAA[A/G]CAGAATAGAGGAAAT | 11124 |
rs540669357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937764 | ATTTTAAGAAAAATG[C/T]CCCTATCTTAATTTT | 11124 |
rs540673099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888942 | TCAGAAGGAATGGTA[C/T]CAGCTCCTCCTTGTA | 11124 |
rs540684918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50618567 | CGCGCCCGGCCACCT[A/G]AATCTTTTTTAATGC | 11124 |
rs540693131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50561569 | GCAGGGGCTCATGCC[C/T]GTAATCCCAGCACTT | 11124 |
rs540693859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50628473 | TTTTAAAGTACCTAG[A/C]CTTTTATCTTCATGT | 11124 |
rs540696466 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50466359 | GTTTTTAGGGGACAG[C/T]AGGAATCAGGAATTA | 11124 |
rs540696491 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50535928 | AATGAGTCTTAGCTC[-/A]AAAAAACCTCTCTGA | 11124 |
rs540696875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50456612 | TAGCTGGGAACATTT[C/T]ATTTCTTCTAATTTA | 11124 |
rs540709840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50681312 | TCAACCTCCCAAAAT[G/T]CTGGGATTACAGGCA | 11124 |
rs540717036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880012 | AGTAGAGAAAAACAC[A/G]TATCATTTCATCTTC | 11124 |
rs540728346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50776555 | AAATACTTAATAGTC[A/C]ATCAAAAAAAAGAAC | 11124 |
rs540732943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50767918 | AACCAGGTAACAATC[C/T]GATGACTGGATCAAA | 11124 |
rs540735967 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50505041 | GAGTGGGGGATCTTA[-/C]TGATCTTATAGAAAG | 11124 |
rs540741431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50823409 | AGCACAGAAGGAATA[A/G]CATAAGCACATAAAA | 11124 |
rs540755024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50919644 | AAGCACCTGACACCA[C/T]GTCTGGCTAATTTTT | 11124 |
rs540762079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50509780 | TTTCAAATACAGACA[A/G]CCTTGCTTTGAATTC | 11124 |
rs540762436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50874886 | GCAGTTCTCCTGTCT[C/T]AGCCTGTAATGTAGC | 11124 |
rs540778438 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50573948 | GCCTGGCCAACAGGG[A/C/T]GAAACCCCATCTCTA | 11124 |
rs540783584 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50752904 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTGAA | 11124 |
rs540787984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50647475 | TATGATTCTGGAGGC[C/T]GCCAATTTGCGAATC | 11124 |
rs540799078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50517176 | CTATTTAAAAACAAA[A/C]TGCTAGAATTCAAAA | 11124 |
rs540809870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810815 | GCACTCTGGGAGGCC[A/G]AGATGGGTGTATCAC | 11124 |
rs540821605 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50922713 | ATCCCAGCTACTTGT[C/G]GGGGCTGAGGCAGGA | 11124 |
rs540838770 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FAF1 | GRCh38.p7 | 1:50640430 | CCTGAGTAGCTGGGA[C/G]TACAGGCGCCCACCA | 11124 |
rs540841216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50661601 | AGACCGAATTTTAAA[C/T]ATATCAAACTTAAGC | 11124 |
rs540852317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50857086 | TTTTCATCTCATTTC[A/G]TTACATTAAGCATCA | 11124 |
rs540861771 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50509777 | GGCTTTCAAATACAG[A/G]CAGCCTTGCTTTGAA | 11124 |
rs540863728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50898065 | AAATAATTGTTGTTT[G/T]CAGCCACTTTACTAT | 11124 |
rs540869510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50488042 | GGCAAATAAGTTTGG[A/G]TAAGATTGGACTAAA | 11124 |
rs540875000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50703976 | CAGTATTTTCCCATC[A/G]AAACAGTAATAAAGG | 11124 |
rs540880200 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50792136 | TGACACCAAGGACTC[A/G/T]AGGATGGCTGCTTCT | 11124 |
rs540888902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50547751 | TTTCTCCTTGTTGCC[A/G]TCTAGAAATAACTCA | 11124 |
rs540890533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50846410 | CATCCCTGCCATCCC[A/G]CCCCTTCGCGTCCTG | 11124 |
rs540899748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50952179 | GCTGGACTGGACTGC[A/C]GCCATCTCGGCTCAC | 11124 |
rs540903653 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50456430 | TACTTCCAAGACCAC[C/T]GTAAGGAGGAGGTAA | 11124 |
rs540905677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50590249 | GTAGACTGCTTTGGG[A/C]ACTACAATATTACGC | 11124 |
rs540911461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50597315 | CCTTATATTCTGGGG[C/T]CTTTCTAAGTTAGCC | 11124 |
rs540913289 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50803359 | AATACTAAGGACTCA[C/G]AAAGTCTAAAGTCTG | 11124 |
rs540923323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50478278 | AAGCGATTCTCCCAC[A/C]TCAGCCTCCCGAGTA | 11124 |
rs540926565 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50824709 | CTAAATGCCTATCAG[C/T]GGATGAAGAGATTTA | 11124 |
rs540934580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50842107 | CAAAAACTTTAAGAC[C/T]CTGTTATACTGTAAG | 11124 |
rs540954426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50472960 | GGCCTAAAGAGTCCT[G/T]GGTGGGCTTTCTTAG | 11124 |
rs540957824 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50789388 | CAACTCAGTATGTCC[A/C]CAGCTTAGTTCATTA | 11124 |
rs540963095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50945247 | GGTTTCTAGGGTCAC[A/G]ATGGCGTGGCCAGAG | 11124 |
rs540970457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50687579 | ACAAGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 11124 |
rs540973904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50641333 | GCATTTAAACTATGA[A/G]TTCTCCTCTAAGCAC | 11124 |
rs540985638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50493166 | GCCTCCCGAGTAGCT[A/G]GGATTACACGCACCC | 11124 |
rs540988563 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50888644 | TTTTTGTCTTTGGTT[C/T]TGTTTATATGCTGGA | 11124 |
rs540991906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895112 | GGTTTTTAGAAAAGA[A/G]AAAAAAATTGACAAA | 11124 |
rs540992171 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50860619 | GATGCTAGTGAGGCC[A/G]CAGATACAAAGGGAA | 11124 |
rs540996250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50523802 | TCCCATTGATGGGCA[C/T]TTAGGTTGATTCCAT | 11124 |
rs540996984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50742423 | GACTCTTGCTCTGTC[A/G]CCCAGGATGGAGTGT | 11124 |
rs541021684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50904269 | CCAGACACAAAGGGA[A/C]AAATACTGTATGATT | 11124 |
rs541025820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50485489 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11124 |
rs541028454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50645864 | GAAAAAAAATAAATC[A/G]GTGTGAATGTGTCCC | 11124 |
rs541040989 | snp | C/T | 0.030665 | 0.119967 | intron-variant | FAF1 | GRCh38.p7 | 1:50637710 | GTGTGTGTGTGTGTG[C/T]GTGCGTGTGCATATG | 11124 |
rs541043452 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50735093 | ATAACTTAAGAAAAG[C/G/T]CCTAATCATCTTAAT | 11124 |
rs541043469 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50449777 | ACAGGCATGAGCCAC[C/T]GCGCCTGGCCTAACT | 11124 |
rs541044812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50751573 | GGTCTTGAACTCCTG[A/C]CCTCATGATCCACCC | 11124 |
rs541049673 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50830659 | CCTCCAGTGCTCAAT[-/T]TTTTTTTTTTTTTTT | 11124 |
rs541055122 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50952712 | GTGGGGAGCGCCTCT[A/G]CCCCGCCACCCCGTC | 11124 |
rs541059371 | snp | A/G | 6.59565e-05 | 0.00574229 | missense, utr-variant-5-prime | FAF1 | GRCh38.p7 | 1:50788075 | AGTCCAGCATCCGAG[A/G]TTGCCTTTCTACAAT | 11124 |
rs541062341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50688057 | GAAGAACAGCGTGAA[C/G]CCGGGAGGTGGAGCT | 11124 |
rs541067334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895872 | AAAAAAAAGCCTCAA[A/C]ACACTGGGTATAGAG | 11124 |
rs541069156 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50711357 | CTTTTGTAGTAGTTA[A/C]TTTTCATGTTTTAGT | 11124 |
rs541085256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50542171 | ATCAAAGAGAGACTT[A/G]AAATTTTAATTAATC | 11124 |
rs541100911 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | FAF1 | GRCh38.p7 | 1:50681834 | TCTTTTGTTTTTTTT[G/T]GTTTTTTTTCCTCTT | 11124 |
rs541103547 | in-del | -/AAA | 0.0360337 | 0.1293 | intron-variant | FAF1 | GRCh38.p7 | 1:50751151 | CACCCATTTCATGTT[-/AAA]AAAAAAAAAGAGCTA | 11124 |
rs541104630 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50857106 | ATTAAGCATCATTAC[G/T]TTTAATCTGAAAAGA | 11124 |
rs541107325 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50496505 | TGAAGTAATTCAGAA[C/T]CTGACAAGGTAGGTT | 11124 |
rs541108064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50896525 | AGATATGGAAGCAAC[A/C]TAAGTGTCCATGAAT | 11124 |
rs541121604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50930618 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 11124 |
rs541122793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50779455 | AACAAGACTTGAAAT[G/T]TGAAATTACTCCATG | 11124 |
rs541135357 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50770000 | ACGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 11124 |
rs541145459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50674749 | CACTTATTTCAGAGC[A/T]TCATTCTCTCAATTC | 11124 |
rs541147966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50884130 | GAAGTACTTAACAAT[G/T]AAGTATAATGATGTC | 11124 |
rs541163300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50808663 | ATAAAGATTTAAAAA[A/C]AAAAAAAAAACTTTT | 11124 |
rs541164667 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812033 | AGACTGAAACTGGGC[A/C]CCTTCCATACAGCAT | 11124 |
rs541165505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50646544 | GAAGACATTTCTTAC[C/T]TCCAATGCTTATAAT | 11124 |
rs541166165 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50488468 | GACGATACACTAATA[C/T]ACACACAAACACACA | 11124 |
rs541175653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50638784 | TTCTATCAGGCTGGG[A/G]AAATTCTTCTCTATT | 11124 |
rs541176418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50748767 | AAATATAATTCAATT[A/C]CATTTACAGTTAAGT | 11124 |
rs541179331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50939514 | TTTTTCATTCCCTAT[C/T]TGAATGCCTGCTCTG | 11124 |
rs541183083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50592774 | CCAACATGGCAAAAT[C/T]CTGTCTCTACTCAAA | 11124 |
rs541184308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50490793 | AAAGGCTCATTGTCA[A/G]CATGACTCAGAGGTA | 11124 |
rs541190336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650330 | CTGAAAGAGTTGGCC[A/G]GGCACAGTGGCTTAG | 11124 |
rs541197809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50736434 | TACTAGGATATTGTT[A/T]GTTTGATTCTATTAT | 11124 |
rs541205301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50711306 | ACTTTAAAATCTTAC[A/G]GTGATAGTGAAACAT | 11124 |
rs541222440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50650749 | ATAAGGTATCTAAAC[A/G]TAATTCACAGTGTTA | 11124 |
rs541222827 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50958598 | CAGGAGAATGGCGTG[A/C]ACCTGGGAGGCGGAG | 11124 |
rs541238145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50763285 | CATAAAATATAAAAT[A/G]AAACAAAATAAAATA | 11124 |
rs541245485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50749397 | TCTTGCAGAAAGCCT[A/G]GGTAACACATGAGAC | 11124 |
rs541255228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50614624 | GTGGGCGGATTACCT[A/G]AGGTCAGGAGTTCGA | 11124 |
rs541255333 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | FAF1 | GRCh38.p7 | 1:50454160 | TCTAAATTTTCGAAC[-/A]GGGGGTAGGGGCTTG | 11124 |
rs541260020 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50726745 | AAGGCAGGAGAATGG[C/T]GTGAATCCGGGAGGC | 11124 |
rs541261343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50457434 | TCTGCGCACATACAC[A/G]TTTGCAGTTGTTTGT | 11124 |
rs541264713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50606627 | GCTTCAGCCTCCCGA[A/G]TAGCTGGGATTATAG | 11124 |
rs541270293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50902687 | CTATAAAATGGCATA[A/G]TATTTGCATATAACT | 11124 |
rs541278299 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50712700 | TGTAATTTGCAAAGA[A/C]ATTTTTGCTAAAATG | 11124 |
rs541287697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50867640 | ATGCGATACCACTTT[A/G]CTCTTGCAAGAATGG | 11124 |
rs541294091 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50500952 | TGAATTATCGTGATA[C/T]AGTAAGAAATATTTT | 11124 |
rs541298374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50598153 | AACAAAAGATTAGCT[A/G]GGTATGGGGGTGCAC | 11124 |
rs541304797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50756676 | ACAGAAGAAAGGGTT[G/T]AACGGACTTATAGTT | 11124 |
rs541308015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50903297 | TACCCTCTAACCCTC[A/G]AAAGAGTTACTTACC | 11124 |
rs541310868 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50869814 | TAAGTTCTATTCTCT[A/G]CAGTTTTACATATTT | 11124 |
rs541313825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50894258 | GAGCCAAGATCACAC[A/G]ACTGCACTCCAGTCT | 11124 |
rs541317145 | in-del | -/AG | | | intron-variant | FAF1 | GRCh38.p7 | 1:50554382 | TATATATATATATAT[-/AG]ATATATATAGAGAGA | 11124 |
rs541320851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50849614 | ACAGACTATATAGAC[G/T]ATAGTGTACTATACA | 11124 |
rs541327560 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50960390 | CCGGCCAGGATCTCT[A/G]CGCTGGCGGCAGAGA | 11124 |
rs541328394 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50936354 | TTTAAAAAAGAAGAA[A/G]AATGAGAAATACAGA | 11124 |
rs541331036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50937219 | GTGCACAACTAGGTG[A/G]AAGTCCACTCTACTG | 11124 |
rs541331128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50607962 | AAAGAATTCAAGGGT[C/G]GACCAGAGGTGTTAA | 11124 |
rs541349596 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50719792 | CCGTAGAGAATACCC[A/G]CAGTTCTTTTTCAAA | 11124 |
rs541356689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50491466 | AAAATTGCTGGTTTC[C/T]ATCATAGACCAACTA | 11124 |
rs541362268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50541058 | AAAAGACAAACGGCA[C/T]TAAAATGTCATGTGT | 11124 |
rs541366523 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641724 | TGTTGGCCAAATCTA[A/C]ATTCTTACCTATCAT | 11124 |
rs541368017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50909603 | TTCTCTAAACTTCTC[C/T]TCTTGCTTCATTTCA | 11124 |
rs541372639 | in-del | -/ACTA | 0.0437281 | 0.141251 | intron-variant | FAF1 | GRCh38.p7 | 1:50790053 | GTCTAATTCCACACT[-/ACTA]ACTAACTATAAAGTT | 11124 |
rs541375031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50909205 | TTGAATATTGGACCC[C/T]ACTCTCTTCTGGCTG | 11124 |
rs541375357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50644465 | ATGCACAGAGACTGG[C/T]ATTCAGCTAAAGACT | 11124 |
rs541381453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50532158 | CTTGAGCTATAACTT[C/T]CATGAAGACACTCTA | 11124 |
rs541386094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50497170 | CAGCTGGAGAAAAGA[A/C]AAGACATAATATGTA | 11124 |
rs541387199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50651701 | GTAACACATTTCAGG[C/T]TGTTTACACAGCTGA | 11124 |
rs541394250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50753826 | GTAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 11124 |
rs541398826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50543113 | GCATAGATATTTCTA[C/T]CTTGTTAACGGAAAC | 11124 |
rs541402725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50705646 | ACAGTAATCATTGAT[A/G]CTCCAGTTAATTAAA | 11124 |
rs541406819 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50952869 | AGGAGCCCCTCTGCC[C/T]GGCCGCCACCCCGTC | 11124 |
rs541415348 | in-del | -/AAGA | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50775677 | AAGATGGACTAAAGG[-/AAGA]AAGAAAGAAACGAAC | 11124 |
rs541417638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50912241 | GTATTAAAGTGTTTA[C/T]GGTGTTGTCCTCATC | 11124 |
rs541418412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50805364 | TTCTGTTTAGCAAAA[C/T]TGACAACGAAAACAA | 11124 |
rs541434279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50655867 | TTTATAATTTATTTA[A/C]TCGTAAAAATGCACA | 11124 |
rs541436962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50648880 | GCGGTGAGCCAAGAT[C/T]GTGCCATTGCACTCC | 11124 |
rs541452516 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50718557 | TTCTTTTCTTGCACT[G/T]TATATTTTAAACAAA | 11124 |
rs541455764 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50547884 | AATAATTGGCTTTTT[A/C]TTACCACTAAGTAAG | 11124 |
rs541456023 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50537320 | GGAAGGCTCCATTGC[A/C]AAACTGGACTTGTAG | 11124 |
rs541461062 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746406 | CCTCCTGGGGTCAAG[A/C]AATTCTCCTGCCTCA | 11124 |
rs541461223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50549721 | TGGGGGTTGCAGTGA[C/G]CTGAGATCCCACCAC | 11124 |
rs541463189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50695800 | ATTACAGGAACCCAC[A/G]ACCACACCTGGCTAA | 11124 |
rs541466604 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50957647 | CTGAGCCACCATGCC[C/T]GGCCGAAATTTTCAT | 11124 |
rs541472395 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50797497 | CTTGAACCCAGTAGT[C/G]TAGAACTCCTGGGCA | 11124 |
rs541483817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50806143 | GATTTATATTAAAAA[C/T]TTATAAAAATTCTGG | 11124 |
rs541486396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793151 | TGACCACTGTGGAGA[A/G]CCACAGTCACTTCCG | 11124 |
rs541488647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50851239 | GCATGCGCCACCAAG[C/T]GGGGCTAATTTTTGT | 11124 |
rs541500227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50688827 | CAAAATAAAATAAAA[A/T]AAAAATAAAAAATAA | 11124 |
rs541500336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50900185 | ACTTACAATGAATTT[C/T]AGCATATTAAAGCCT | 11124 |
rs541500950 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | FAF1 | GRCh38.p7 | 1:50475552 | ACAATCTGGAGCTTG[C/T]TGCTGGCCAGGAAAC | 11124 |
rs541508019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50844178 | CATCTGTATGTCATC[C/T]TTTGAGAAATGTCTA | 11124 |
rs541514014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50538635 | AGGGTCTAGTCTGAT[A/G]TCTACAAACCACACC | 11124 |
rs541524257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50854611 | AAGTGGAGCCAAGTG[C/T]AGAGTACTTAAAACA | 11124 |
rs541527852 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50530703 | CCATTCTCCATGATG[C/T]GCTTATTTCGCATTG | 11124 |
rs541535073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50790117 | CCACTGGAATATAAG[C/T]ACCACAAGAATAAAG | 11124 |
rs541540777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50689392 | GATACAGACCATCCT[C/T]GCTAACACAGTGAAA | 11124 |
rs541546772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50844659 | CGGGAAAAATGAATA[C/T]AAAGAATCTGGAAGA | 11124 |
rs541551273 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50569941 | AAAACGGCATCTCTT[C/T]GGCAATATTTAATTT | 11124 |
rs541554001 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50446382 | AATCCAAAACTTTTT[G/T]AGTGCTGACATGATG | 11124 |
rs541555206 | snp | A/G | 0.000399281 | 0.0141238 | missense | FAF1 | GRCh38.p7 | 1:50584796 | TATCACTAACCATAT[A/G]AACATCGGTGATTTG | 11124 |
rs541557903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534601 | TTTTGAAAACCCTGC[C/G]CACATCTTTAAAAAT | 11124 |
rs541562405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50642173 | GTGCCACTGCACTTC[A/G]GCCTGGGCAACAAAG | 11124 |
rs541572267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50649554 | TCTGAATCCTAACAC[A/G]CGCCCAAAGAGCTTT | 11124 |
rs541583451 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50793794 | TGACATTCCAAAGAA[C/G]GATACTACACTGATG | 11124 |
rs541584852 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50771977 | ATGCAAAAAAAATTG[A/G]CAGAAGTAGAGCCCT | 11124 |
rs541585187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50489901 | ATTTGCCAACAAATA[A/T]TTGTTGGCACAAAAG | 11124 |
rs541591193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50449311 | ACAACCAGAAATTGT[C/T]GGGGCTCAAACTTGA | 11124 |
rs541607200 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50643789 | GTAGAGCTGGGGTTT[C/T]GCCATGTTGGCCAGG | 11124 |
rs541612944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50625120 | GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTTAG | 11124 |
rs541613748 | snp | A/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50900515 | GCATAGGCTTTGGAG[A/T]CAGACCAGTCTGACT | 11124 |
rs541619534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50517892 | AGTTATTAAAACAAA[C/T]GAAAGAACAATAAAA | 11124 |
rs541631278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50513949 | TATTTCTCCATCTCT[A/G]CATTTTCTTCCTTCC | 11124 |
rs541634217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50915269 | CGGCTACTTGGGAGG[C/G]TGAGGCACGAGAATC | 11124 |
rs541636606 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50605441 | CCTTTTTAGAGAGAA[C/T]GGTCAACTTTACCTA | 11124 |
rs541642688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50557558 | TTAGAACATTAAGAT[G/T]GTTGGGCTTTAAAAT | 11124 |
rs541645827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50870443 | GCCTGGGTGACAGGG[A/C]AAGACTCCATCTCAA | 11124 |
rs541646165 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50565894 | ATTTAGCCAAGTCTC[C/T]AGTCTCTGTATTTTG | 11124 |
rs541652550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50811820 | TGACTTCAAACTATA[C/T]CATAAAGCTGCAGTA | 11124 |
rs541653378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50452949 | CCCTCTGGGTCTATC[C/T]CCTTCACACTTCCAC | 11124 |
rs541671131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50723559 | AGTGGCTAGAATGGC[C/T]TCAGTACAGGATGAC | 11124 |
rs541673583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50871171 | CAGGTGAGGACACGC[A/G]GAAGAAAAGTTTGAA | 11124 |
rs541674089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50915755 | GAGATGTTGAAATAA[A/G]TATTTCAGGCTCATG | 11124 |
rs541674632 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50638405 | AGTGAAAGTATTCCC[C/T]CATTAAATACGGTAG | 11124 |
rs541695067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50570569 | TTAGACTGAATGTGA[A/G]AAAGGAGATGATAAA | 11124 |
rs541696419 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812480 | ACGAAAAAATGCTCA[A/G]TATCACTAATCATTA | 11124 |
rs541707223 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50558581 | GATGACCAAGGAGAA[C/T]ACCAACAGACTTATA | 11124 |
rs541727703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50445133 | AGGTGGTTTTTGTTA[C/T]ATGGGTATGTTCTTT | 11124 |
rs541728132 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50716318 | CTTCAGTAGACAGAA[G/T]AATTAGCTAAACTAA | 11124 |
rs541728241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50760231 | AGACTCCCACACATT[A/G]ATAATGGGAGACTTT | 11124 |
rs541736590 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50925941 | GAATTGGGCCAGATG[G/T]AGTGTGCCTCATGCA | 11124 |
rs541737128 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961561 | GTCATGGGGCATTTA[C/T]TTGCTTTGGAAAGTA | 11124 |
rs541755118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50505012 | CACTGCTTGTAAGAC[C/T]GTAGAAGTCTTCTGA | 11124 |
rs541758560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50611500 | TGTGAGGCTAATTGT[A/G]GATCTTGAGTTAATT | 11124 |
rs541759604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50906358 | TATTGTCTTGGCAAT[A/G]CAGGCTCTTTTTTGG | 11124 |
rs541765927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50488858 | TTAATACACAGAAGA[C/T]ATTCAACAAAATATT | 11124 |
rs541768638 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50805659 | CCTACATGGAATGCT[A/G]GGATATCCTTTCTCT | 11124 |
rs541772165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952678 | GAGCATCTCTGCCCG[C/G]CCGCCCATCGTCTGA | 11124 |
rs541775872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50824914 | TATCTCATGAAAGTA[A/G]AGAGTAGAATGATGG | 11124 |
rs541783457 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50955574 | CTATAGAAAACAATA[C/T]GACAGTTCCTCAAAA | 11124 |
rs541804534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50585048 | AGAATGCTTACAAAC[C/T]AAATAAAGACAGGGA | 11124 |
rs541809158 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50907172 | GTTCTGTTTACACAA[C/T]GGATTACGTTTATTG | 11124 |
rs541812774 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FAF1 | GRCh38.p7 | 1:50690532 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 11124 |
rs541815847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50501303 | TGCTGTCTCATTAAT[C/T]GTCAAGAAAATGCAA | 11124 |
rs541816650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50446002 | CCTGGGCTTCAGTTC[C/G]TTTTCTAAAAAGCCT | 11124 |
rs541818413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50563801 | GTTCATATTTGGAAT[C/G]TTCTAAGATCAACCT | 11124 |
rs541820377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50554813 | AGGTCAAATAGGTGA[A/G]TCACTCTCTTTTCAT | 11124 |
rs541828796 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FAF1 | GRCh38.p7 | 1:50817940 | TAAAAGGCTCGAAAA[A/C]GGTAAATACTATATG | 11124 |
rs541829705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50709137 | GAGCTTGTCTGACAT[C/T]CCCTCATGTCAAAAA | 11124 |
rs541838075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50446896 | CTGTAGATTAGGAAA[C/T]AAGACCCAGAGACTG | 11124 |
rs541848962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50921970 | CCAGGAGTTCAAGAC[C/T]AGCCCGGCTAACATG | 11124 |
rs541856111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50956002 | GAGAGAGGGATATAA[A/G]GACTTATTGTTAAAT | 11124 |
rs541859023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50562995 | TAACAACTATTTACA[C/T]AGCACTTACATTGTA | 11124 |
rs541865011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50515687 | GCTTAAGAGAAGCGA[C/T]GAATACTTACTGCCC | 11124 |
rs541892004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50810054 | TGAGGTCAGCAGTTC[G/T]AGACCAGCCTGACCA | 11124 |
rs541892022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50818730 | ATATGCGCAGACCCA[C/T]AATAAGAAATCTTGG | 11124 |
rs541893140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50700889 | CAGTTCCAAAGAGCT[A/G]CATTATAAATATTAA | 11124 |
rs541901699 | snp | C/T | | | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459501 | GATTTTTGCTTATGG[C/T]ACTATACCATCTTTT | 11124 |
rs541905339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50701630 | ACAACATACAAAATC[C/T]GACGTTAGGTTCAAA | 11124 |
rs541912404 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50782014 | TATTCATAAATTTTT[C/G]GTGATGCTGGTATAA | 11124 |
rs541913241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50846857 | AGAAGATTCACCAGG[A/T]ATTAGCCTTATATTT | 11124 |
rs541919536 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FAF1 | GRCh38.p7 | 1:50949996 | CACACCCAGCTAATT[A/T]AAAAAAAAAAAATTT | 11124 |
rs541945352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943164 | CCACTATCAGGCACT[A/C]TGATTAATCCAACTG | 11124 |
rs541950208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50847386 | AAGCCAGATGGGTAA[C/T]TACAGCAAAAAAAGA | 11124 |
rs541953925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50739764 | TCTGGTGTTACCTAT[A/G]TATCTTTTACTCCAG | 11124 |
rs541962278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50588202 | TGAGGCAGGAGAATC[A/G]CTTGAACGTGGGAGA | 11124 |
rs541970509 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50911560 | AAATTAACCAAGCCT[C/G]GTGGCACCTGCCTGT | 11124 |
rs541973042 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50914355 | AGAAGCATTTTTAAT[A/G]TAAGCTAGAATAAAA | 11124 |
rs541985710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50657601 | ATAGGGTTCTTCATA[C/T]TTCAACAAGCATCAT | 11124 |
rs541987351 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50750366 | ATGATAAATAAGAAT[G/T]TAAAACATTAACTTA | 11124 |
rs541987940 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50812721 | CACCATCATTACTGC[A/G]TATATACCCAAAGGC | 11124 |
rs541999345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50822806 | TGAGACGCAGTTTCG[C/T]TCTTGTTGCCCAGGC | 11124 |
rs542000166 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FAF1 | GRCh38.p7 | 1:50530790 | CCAAAAAATGAAACA[A/G]ACAACCAACAAGAAC | 11124 |
rs542007114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50722966 | CTAGAGCTTTCCTCT[C/G]AATTCTAAGTCAGAG | 11124 |
rs542016338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50740563 | AAATACACTCTGGCG[C/T]TTCCTATTGTATTCT | 11124 |
rs542016901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50513313 | GGAGAAACCCTGTCT[C/T]TACCAGAAAAAAATA | 11124 |
rs542024651 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50817260 | TGTCAATCAACAGAC[A/G]GATAAGCAAAATGTA | 11124 |
rs542029252 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50498475 | AGAATGGAAGAAAAT[A/G]TTTGCACGTGATGTC | 11124 |
rs542034864 | snp | C/G | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50467877 | CAGATGTGCTAATTA[C/G]CTTGATTTACTCTTT | 11124 |
rs542039826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50452271 | CATTGCCCCTGAAAG[C/T]ATAAACTGGACACAG | 11124 |
rs542054684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50815364 | AGGATTATGGCCTCC[A/G]GCTGCATCCATGTTA | 11124 |
rs542057033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50943923 | TCTAAGGAGAACCTA[C/T]ATCAGTCAAGGAGGC | 11124 |
rs542076280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50610747 | ATGGGAAGCCACACC[C/G]CTCACACCTGTTAGG | 11124 |
rs542076289 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FAF1 | GRCh38.p7 | 1:50934286 | ATACTTACCCATATA[C/T]ATGAAATTTTCAGTG | 11124 |
rs542088560 | snp | C/T | | | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462529 | TAAATATCAACAACT[C/T]CTCCCCTTTTTAAAG | 11124 |
rs542096775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50662734 | GGAGTCTCCCTCTGT[C/G]GCGCCCAGGCTGGAG | 11124 |
rs542099806 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50692934 | TCTTTTTATTATTGA[C/G]TTGTAAGAGTTCTTC | 11124 |
rs542105480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50552477 | CAAATAATTATTTAG[C/T]ATTTTAATAGGAAAC | 11124 |
rs542105708 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50681127 | TCTCAGCTCACTGCA[A/G]CCTCCGCCTCCCAGG | 11124 |
rs542105777 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | FAF1 | GRCh38.p7 | 1:50561878 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 11124 |
rs542112655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50786214 | CAACCTAAATGTCCA[A/T]TTATGATGTTAATGA | 11124 |
rs542117797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50816017 | AGGCGATAGAGTGAG[A/G]TTCCGTCTTAAAAAA | 11124 |
rs542125498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50911775 | TGGTGCCTCACGCCT[A/G]TAATCCCAGCACTTT | 11124 |
rs542133582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50655167 | AGTGGGATTAGAGGC[A/G]GCCGCCACCATGCCC | 11124 |
rs542136174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50671329 | AGAATCACTTGAAAC[C/T]GGGAGGTGGAGGTTA | 11124 |
rs542146087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50862913 | GAAATGAGATGATGG[C/T]AACACAGTAATAGCA | 11124 |
rs542147385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50888032 | ATGTTCTTCCATTTG[C/T]TTGTATCCTCTTTTA | 11124 |
rs542158201 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50664391 | CAAACTCACAATAAA[A/T]GACCTATTGGTCTCA | 11124 |
rs542159108 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50522151 | GAATATAATATTTGC[A/G]AATATGGCAATGTCT | 11124 |
rs542168078 | in-del | -/CTCT | 0.00557542 | 0.0525036 | intron-variant | FAF1 | GRCh38.p7 | 1:50611400 | CTAGTTATTATAAGC[-/CTCT]CTGTTTCAAGTGCAA | 11124 |
rs542169378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50820354 | ATGGGGTATAACTGA[C/T]AAATAAAAGTTGTGT | 11124 |
rs542174144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50833163 | AGGTTTAAAAGTCCA[A/C]AAGATTGCCCTCACT | 11124 |
rs542193069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50486548 | TCACATCTCTACGGG[C/T]GCACCGTGAAGTCTT | 11124 |
rs542193375 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50684053 | TATAATGTGAAAGGA[A/G]ATCTTTCAGCTAATT | 11124 |
rs542197089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50627433 | AAAACTATCTAAATG[C/T]CTGCCTCATCAATAG | 11124 |
rs542204998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50717341 | AATTAGTGTTCTTAT[A/G]AGAAGAGAAAGACAG | 11124 |
rs542223297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50518998 | TTTCTTCAGTGAAAC[A/G]ACAGTGGGCAGTTGA | 11124 |
rs542224385 | snp | G/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50752786 | CTCCCGGGTTCAAGT[G/T]ATTCTCCCGCCTCAG | 11124 |
rs542234779 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50959379 | GCCCATAACACCACA[A/C]GCTCCACGCTCACAC | 11124 |
rs542235602 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FAF1 | GRCh38.p7 | 1:50619921 | TCTCTTTTTTTTTTT[C/T]TTTTTGAGACAGAGT | 11124 |
rs542246706 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50880283 | TAATTAAAAAAAGGG[-/A]AAAAGGGCTATCACA | 11124 |
rs542249902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | FAF1, LOC105378715 | GRCh38.p7 | 1:50459233 | CCCACCTTGGCCTTC[C/T]AAAGTGCTGGGATTA | 11124 |
rs542251277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50504752 | CTATAGAATACCAGC[C/T]CTGATTCTTAATGCT | 11124 |
rs542253608 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50686112 | TATGATAATGTAAAC[-/G]GTACCCAATAATAGT | 11124 |
rs542254789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50821012 | TGGTGCAAAAGTAAT[G/T]GCGGTTTTTGCCATT | 11124 |
rs542270370 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50620552 | AATTCTGTGTCTGTC[A/G/T]TTGCAGTCATTTTGG | 11124 |
rs542270646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50612381 | AAATAAAGAGGTTCC[A/G]TTAGTGGAGAAACCT | 11124 |
rs542273705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50957508 | AGGCGCCCGCCACCT[C/T]GACCGGCTAATTTTT | 11124 |
rs542275380 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50709063 | CTTCCTGAGGTTTGA[A/G]GGCCTTTCAAAGGTA | 11124 |
rs542281169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50559609 | TTGCTGCTGGCAGAA[C/T]GCAAACCTTGAGTTA | 11124 |
rs542288598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50916927 | AAATGAACCAAGCTG[C/T]AGTTTTAATTTTTAA | 11124 |
rs542289258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50813469 | TTTCCTTTTAAAAAA[A/T]TTTTTTTTTGAGACA | 11124 |
rs542291654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50821606 | CACTTACTAGGAGCA[G/T]AATTTTGAGAAAGTT | 11124 |
rs542299854 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FAF1 | GRCh38.p7 | 1:50961762 | GGCTTCCAACTCCTG[C/T]GCTCAAGCCATCCTC | 11124 |
rs542303276 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | FAF1 | GRCh38.p7 | 1:50864125 | CTTGCTAGCGGTCTA[A/T]CAATTTTGTTGATCC | 11124 |
rs542316268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50558848 | TGCATGTGCAACCAG[A/G]CAGTTATAACTGTAG | 11124 |
rs542322819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50907302 | TTTTATTGAGGATTT[C/T]TGCATCGATGTTCAT | 11124 |
rs542323326 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50641405 | TTTTAATTTAGTTTA[A/C]AATGTTACCAATCTT | 11124 |
rs542337588 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50451435 | AAATGAGGACAAGAG[A/G]CTCAGCGAGATTATA | 11124 |
rs542337821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50498653 | TCAGGAGTTCGAGAC[C/T]AGCCTGACCAATATG | 11124 |
rs542343158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50507776 | ATTTGAGCAGTGAAA[C/G]GTTTTTAAAAAATTT | 11124 |
rs542357425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50856168 | CCTCCATTAAAGACT[C/T]GTACTCCCAGCCCAC | 11124 |
rs542361030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50952949 | CGGTTTTGTCGAATA[C/G]AAAAGGGGGAAATGT | 11124 |
rs542361069 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50672535 | CAATCTGCCTACCTC[C/G/T]ACCTACCAAAGTGCT | 11124 |
rs542367153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50528967 | TTCACTTTATTAATG[C/T]GCTATATAATACATA | 11124 |
rs542376145 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50909808 | TTTTTAGCTTCTTTG[A/C]GATGGGTTTGAAGAT | 11124 |
rs542377978 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50854911 | CAAAAGGAAATGCTC[A/G]ATGGAACATTTTGGA | 11124 |
rs542385003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50755359 | GCTCCAAAATGATCT[C/T]CTTTGACTCCAAGTC | 11124 |
rs542385859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50935235 | ATCAATTAATGCCAA[A/C]ATTTTATAATTAATA | 11124 |
rs542385909 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50634245 | TCTATTTTTGCACAT[A/C]AAAAAAAAAAAGAAT | 11124 |
rs542389392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50865800 | ATATGTAACTAACCT[A/G]CACATTGTGCACATG | 11124 |
rs542392656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50512594 | TTCCATTGGTCTATA[C/T]ATCTGTTTTCGTACC | 11124 |
rs542393419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50589077 | GCACAGTGGTAGGGG[C/T]AGGAGCCAAGGGGCA | 11124 |
rs542397972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50645769 | GGAGGCGGAGGTTGC[A/G]GTGAGCTGAGATCAC | 11124 |
rs542408935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50583574 | AAACTTTAAACAATC[C/T]ATAATTAAAATTGCC | 11124 |
rs542423146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50895770 | GTGACACATCATATC[A/G]ACAGAATGAAGGACA | 11124 |
rs542432384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50534032 | CCTCAGGATCCATGT[C/T]CTCTACACAGCTTTT | 11124 |
rs542437659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50525006 | TTCTTCTACCTCAGC[C/T]TCCCAAGTAGCTGGG | 11124 |
rs542439420 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50832208 | AAACCATCCTCTACT[A/C]CAGTCCGCAGAAAAA | 11124 |
rs542444744 | in-del | -/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50927726 | ATTTGTTTAAACAAA[-/T]TTTTTTTCTTACAAT | 11124 |
rs542450117 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | FAF1 | GRCh38.p7 | 1:50503617 | GATTCCCTGTCTCTT[A/T]AAAAAAAAAAAAAAA | 11124 |
rs542454887 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50789187 | TCCCTTTTATATCCA[C/G]TATCTTTGACATCTC | 11124 |
rs542462411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FAF1 | GRCh38.p7 | 1:50767341 | CATCTACATCTCACT[A/G]GTGTCCCTGAAAAAG | 11124 |
rs542462759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50732532 | TTGCCTTAAATTCAA[C/T]TTTATGTGATATAAA | 11124 |
rs542468475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50889527 | ATTTCCCTCTACACA[C/G]TGCTTTAAATGTGTC | 11124 |
rs542475248 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50575187 | TGCTGGGATTACAGG[C/G]GTGAGCCACTGCGCC | 11124 |
rs542482909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50835685 | GTAGCTGCTGAAAGA[A/C]TTTAATAAGATTCAT | 11124 |
rs542483270 | snp | C/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50746006 | CCAGGCTGAGGAGAG[C/G]TCAGATGGAAATAAG | 11124 |
rs542487087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50471106 | TTGCACAGCAAATGT[C/T]TTGCTATAATGAGAG | 11124 |
rs542496150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50682678 | ATATATACTGGTATT[A/G]TCTCAGCCATTTTGA | 11124 |
rs542503350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50485861 | ACATGGTGGCAGGGG[A/G]GAGAGAGAGAGAACA | 11124 |
rs542506894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50880975 | CTATATAAAAGAATT[A/G]CCTGGATATATATAT | 11124 |
rs542511252 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FAF1 | GRCh38.p7 | 1:50780446 | ATGCTGGGTACAGAG[C/T]TATCATCTTTGACCG | 11124 |
rs542516491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50931409 | TGGAAACAAAAAGAG[A/G]TTTAATTGGACTTAC | 11124 |
rs542518278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50923487 | GATGGCTTCACTGCT[A/G]AATTCTACAAAACTC | 11124 |
rs542518967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50769076 | GAGAAAGAGAGAGAG[A/G]TAGCTCCAAATAAAC | 11124 |
rs542527182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FAF1 | GRCh38.p7 | 1:50824504 | AAAAAGGAACACTTG[C/T]ACATTGTGGGTGGGA | 11124 |
rs542528833 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50526548 | ACTGCAAGCAATCCA[C/T]GTGCCTCTGCCTCCC | 11124 |
rs542528890 | snp | A/C | | | intron-variant | FAF1 | GRCh38.p7 | 1:50564375 | TCCAAACTTACATCT[A/C]TCATAAAGAAATAAC | 11124 |
rs542534750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FAF1 | GRCh38.p7 | 1:50675797 | ATATCCAGAAACAAA[C/T]GTTTATGATACAATG | 11124 |
rs542538702 | snp | C/T | | | intron-variant | FAF1 | GRCh38.p7 | 1:50949362 | AAAATTCTTTACTAT[C/T]GGGCGATGCCTGTGC | 11124 |
rs542548009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FAF1, LOC105378715 | GRCh38.p7 | 1:50462666 | ATTTGCATTGAACAC[A/G]CTGATACTCTACAAA | 11124 |
rs542561836 | snp | A/G | | | intron-variant | FAF1 | GRCh38.p7 | 1:50888995 | AATCCATCTGGTCCC[A/G]GACTTTTTTTGGTTG | 11124 |