| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs183317065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236239 | AAAAATCTTAAAAGC[A/G]GCCAGAGGAAAAAAA | 55120 |
| rs183318422 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220020 | GAGAGCAAAATAAAG[C/T]AGCTCGGTTCTAATA | 55120 |
| rs183328744 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58203174 | TATGGATCTTAAAAT[C/T]AGACCTACATACATA | 55120 |
| rs183334636 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58186617 | AGAGCATTTTTTTCC[A/G]GCTTCCATGCCACTG | 55120 |
| rs183356987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235197 | TATACACAGAGAAAC[A/G]CCAGCGAATTTCAGA | 55120 |
| rs183378632 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202204 | AGTTTGACAATTAGT[C/T]GCTGGTGGTTTTATA | 55120 |
| rs183466720 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239613 | CTATCTTAGATAATA[C/G]TATATCATTAAATAT | 55120 |
| rs183474264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58221819 | GCAACAATAAGGATC[A/G]AATACTCTAGTTACA | 55120 |
| rs183479202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206346 | TAGAAACATGGAAGT[A/T]GTAAACATGAATATT | 55120 |
| rs183510037 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192801 | CTAACAGCCAAAAGT[C/G]TTTGCCCCTGGAGAA | 55120 |
| rs183599592 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58199606 | GTCATATAAAAACTG[A/G]CAGTCATGAGGACAA | 55120 |
| rs183610870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58184460 | AATTCTTAACAGGAA[C/T]AGCAAAACAACTGTA | 55120 |
| rs183716902 | snp | A/C | 1.95884e-05 | 0.00312951 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163547 | GATTAAATCTTTTAG[A/C]AGTAGAACAGCTCAT | 55120 |
| rs183793807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167287 | GGATATTGACGGTAT[A/C]ATGTCTGTTCTCTTC | 55120 |
| rs183827302 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58228189 | AAGTAAAACCTGTTA[C/T]AATAAAATGGCAAAA | 55120 |
| rs183843125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193109 | GACCTAAGTAAATGT[A/G]GAGATAAATGTTTTT | 55120 |
| rs183908012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58240556 | TCTTTTAAAAATTTC[C/T]GCCTCAAAGGGCTGA | 55120 |
| rs183912444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58223517 | CATTTATACACTCTA[C/T]CTTCTATTCTGAGTC | 55120 |
| rs183922039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207867 | TTCAAGACCAGCCTG[G/T]GCGACACAGTGAGAC | 55120 |
| rs183938116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176496 | CTACAACTACCTGAT[A/C]GTTGACAAACCTGAG | 55120 |
| rs183939860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58190668 | AAACCTTTACATCAC[A/G]TAAGTTCAAAACTAA | 55120 |
| rs183958650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233589 | GAAGACAGGGTACAC[A/G]ATAAACCTCAAATTA | 55120 |
| rs183970225 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217241 | ACACACACACACACA[C/T]ACATATATATGTTTG | 55120 |
| rs184000347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | FANCL | GRCh38.p7 | 2:58188716 | AAGTGTTGGGATTAC[C/G]GGTGTGAGACACTGC | 55120 |
| rs184002134 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242655 | CCCCAGTTTATTACC[A/G]TTAGACCATGCTTTG | 55120 |
| rs184020155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210463 | TACAATTCAAGATGA[C/G]ACTTGGGTAGGGACA | 55120 |
| rs184020559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164738 | CTACATTTCTTTGAA[A/G]AAAATATTTTCATTC | 55120 |
| rs184026449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177869 | AGAAGAAAAGAGAGA[A/C]GAATCAAATAGACAC | 55120 |
| rs184032917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179533 | AACTGGCTAGCCATA[C/T]GCAGAAAACTCAAAC | 55120 |
| rs184091714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169747 | ACAGCACGAGAACTT[A/T]GTGAAGCATACACAA | 55120 |
| rs184111605 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58233049 | ACAGTTCTGACTTTC[A/G]TTACATTTAAATGTC | 55120 |
| rs184168789 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58187408 | CATCACACACTGGGG[C/G]CTGTCGTGGGGTGGG | 55120 |
| rs184213118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58230574 | ATTAAGTAACTCTTC[C/T]AAGGAATTACTTTTA | 55120 |
| rs184216540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212408 | AACTCAAGATGAGAT[C/T]TGGGTGGGGACACAG | 55120 |
| rs184226656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195558 | ACACAACAGAAACCA[C/T]AAGAGAAGGATGTGA | 55120 |
| rs184236479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181789 | TGGAGGGGGGAATGA[A/T]TCTCAAAAATATTAA | 55120 |
| rs184484029 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58237455 | GTGTGTGATATAGCT[A/C]AACCAGTATTCAAAA | 55120 |
| rs184497995 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160319 | TTTTGCAAGAGTAAG[A/G]GATGTATTTCCTGAG | 55120 |
| rs184500895 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220890 | GAAATAATAAATGAA[C/T]ACTAAAATACTATTG | 55120 |
| rs184505418 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58174489 | ATTAAGAAACTCACT[C/G]AAAACCGCTCATCTA | 55120 |
| rs184505637 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 2:58243654 | AAAGATTTCCAGCAC[A/G]TTTATTGCTAATTTA | 55120 |
| rs184506971 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241561 | CCACAGGACTGACTG[A/G]CCAAGATCATTCTAG | 55120 |
| rs184507342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203658 | AAAATACTTAAAAAA[A/C]CCCAGCCAAAGCAAA | 55120 |
| rs184509248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58229089 | ATACTTCTTTGCAGC[C/T]TTAATGCTTTATGGG | 55120 |
| rs184655871 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225967 | GCAGCTATAAGAAAT[C/T]ATTAACTTTATTGAG | 55120 |
| rs184656873 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58234290 | AAATGAGAAATTGTA[C/T]TTTAAAAAATGAAAA | 55120 |
| rs184660438 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58171688 | AGCGACGCAGAAGAC[A/G]GGTGATTTCTGCATT | 55120 |
| rs184670867 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58200296 | CAGCTTTCTTTGGTT[A/C]CAGCTCTGCTAACTA | 55120 |
| rs184741617 | snp | A/G | 0.00028309 | 0.0118939 | intron-variant | FANCL | GRCh38.p7 | 2:58241208 | TAGAAAGCAACCACT[A/G]GGCGGGTACCTGAGC | 55120 |
| rs184755765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225115 | ATAAAGAGCCAATAT[G/T]AAGGGACTTGTGCTG | 55120 |
| rs184803941 | snp | A/G | 0.137527 | 0.223271 | intron-variant | FANCL | GRCh38.p7 | 2:58173966 | GCAAATGGAAAACAA[A/G]AAAAGGCAGGGGTTG | 55120 |
| rs184809303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217981 | GTAAACTTCAAAGTA[C/T]TGAGATAATTAAAAG | 55120 |
| rs184811805 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171052 | CTACACAACTCTCCA[A/C]CCCAAATTAACAAAA | 55120 |
| rs184819934 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58184830 | AAAGTCCCCCAAAAC[A/G]GGAGGAAACATCGTG | 55120 |
| rs184834219 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172280 | ACCTGGAGATCTGAG[A/T]ACAGGCAGACTGCCT | 55120 |
| rs184838744 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58220394 | GTGGTTAAAACAAAA[A/C/G]GGAAAAAATTGATCT | 55120 |
| rs184859259 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58186894 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 55120 |
| rs184861957 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58181310 | TAGGAAAGAGTACAT[A/G]CTGTATGCCTCTGTT | 55120 |
| rs184937158 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58236811 | GAAAGATGCAATCTA[C/T]ATGTTAATATTGGAA | 55120 |
| rs184952992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58203350 | GGACAAACACAATTG[A/G]TCTTTTCATCACTAC | 55120 |
| rs184957841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169455 | GATGAGGAAAAACTC[A/G]CACAAAAAGGAGGAA | 55120 |
| rs184984034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211382 | AGTCCCTAGCCTGCA[C/T]ACAGTGCTGGGACCC | 55120 |
| rs184994056 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58198757 | ATTAGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 55120 |
| rs184997403 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180864 | AAAAAGAAATCGAAA[C/T]TTTTCAGAAAAAAAA | 55120 |
| rs185003183 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58183810 | GTTGATTCAATGAAA[A/T]TAACATTTTAGCCAT | 55120 |
| rs185098777 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58194141 | AAAAATATAAAGACC[A/G]CTATTTACTACACCA | 55120 |
| rs185216610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234984 | TTGAAATAAGGGAAA[C/T]AAATGTGAAAATGCC | 55120 |
| rs185220845 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219117 | TACAAAATTTCTTTC[A/G]GTGCCAGAAAGTAAA | 55120 |
| rs185232049 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201780 | TAAAGGACATCTAGT[C/T]AAAATAGGTATTTGT | 55120 |
| rs185440106 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162756 | TCAGAAGTCTGTGTT[A/G]TAATATTTTTCTAAT | 55120 |
| rs185453654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168972 | TTATAGATAAAACTC[C/T]CATCTCCCTGGGACA | 55120 |
| rs185471629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229935 | AAAAACTTATTTGTA[C/T]GCTAACACAAACATG | 55120 |
| rs185474011 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58164957 | AGTATAAAAATTGCT[A/C]ACTAACTTGGATGTG | 55120 |
| rs185493567 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58194865 | CAGCAGGAAGACAGG[G/T]ACCATAAGGAAAATT | 55120 |
| rs185503348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58166029 | ACTCTCCCTGCTTCA[C/T]ATCTCTTCCTACAGC | 55120 |
| rs185505390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178853 | ATCTCAGCCCAAAAT[C/G]TCCTTAAGCTGATAA | 55120 |
| rs185592577 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241946 | TATAAAGCAAAACAT[A/G]AGTAAAGATTGCTGA | 55120 |
| rs185595203 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58226343 | ATAAAATGAAGCCTA[A/C]TAAGTTTTTCAGATA | 55120 |
| rs185603447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210205 | CACACCCAAGACTTG[A/G]CAATTTACAAAAGAA | 55120 |
| rs185612924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191597 | TTCATTTTTGAGCAT[A/G]GAAAACTCCTTGTTT | 55120 |
| rs185620488 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190894 | ACAAAAAGATGAGGG[G/T]GGAATATTTTCTAGC | 55120 |
| rs185622179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179086 | GGAAATAAGAGAGGA[C/T]ACAAACAAATGGAAA | 55120 |
| rs185624492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58216217 | GGCAGCAATCAGAGG[C/T]AGACTGACCTCTATG | 55120 |
| rs185709887 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159297 | TACACAAAATAAATA[A/C]TTGGATAACTCACGT | 55120 |
| rs185749937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208369 | TGGCACTCCACTTTG[C/T]ATTTATCATTTGCTA | 55120 |
| rs185763808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178397 | CACGATCAAGTTGGT[C/T]TCAACCCTAGGATTC | 55120 |
| rs185774067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167184 | GCCACTGCACTCCAG[C/G]CTGGTGACAGAGCTA | 55120 |
| rs185903627 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172831 | GCTTCAGACCATCAA[A/G]CTACTATGAGCTACA | 55120 |
| rs185926077 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58175642 | ACGTATCTCAAAATA[A/C]TAAGAGCTATCTATG | 55120 |
| rs186125250 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58185838 | AGGGAATATAATTTT[A/C]GTCAAGGAGTCAGTA | 55120 |
| rs186131605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209087 | TCTCCTCTAAGAACT[C/T]TCCTAAATTATTTGT | 55120 |
| rs186152999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196720 | GGCATTGCAAACTTT[C/T]CCACAGATAAATGCC | 55120 |
| rs186156887 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58237844 | TAAAGCAGAAGTAAA[C/T]GTGTGTGACTTCAGA | 55120 |
| rs186159022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58221070 | TACAAAAAATTAGCC[A/G]GTCGTGGTGGCAGGC | 55120 |
| rs186163091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183050 | ATGTATAAAAATTGG[C/G]AGCCATTATTATAAG | 55120 |
| rs186167218 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204694 | ACAAAAATCTAGCTG[C/G]TATTTGTTCATATAC | 55120 |
| rs186198595 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58172670 | ACCAAAAGTAGATAA[A/C]ACCACAAAGATGGGG | 55120 |
| rs186218076 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235389 | AATGTAAGAGCCATT[A/T]AATAGAGTGCTCAGA | 55120 |
| rs186225244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239586 | TCATAAACAAAATTT[A/G]AAATATGGACTCTAT | 55120 |
| rs186229660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221696 | TGAAAGTATCTATTA[C/T]GGTAACATCTTACTG | 55120 |
| rs186239259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202426 | AAAGACAGCTATGGT[G/T]TATATATGAAAGCTA | 55120 |
| rs186241774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58206075 | AAAATGAAGAATTGA[C/T]AAAAATTGGGAAGTA | 55120 |
| rs186252134 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188479 | GGGTCTCTCTGTCAC[A/C]CAGGCTGAAGTGCAG | 55120 |
| rs186273682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191200 | GTCAGGAACAAAACA[A/T]GAGAGAATGTTAATA | 55120 |
| rs186290632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218600 | TAAGTAACTGAAAAT[A/G]AGTGAAGCCTATAAA | 55120 |
| rs186306543 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58201047 | GATGATTTATCATAA[A/G]TATTAAAATATAAAC | 55120 |
| rs186313367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185411 | CACACATACTGAAAA[G/T]ATTTCTGAACAAACC | 55120 |
| rs186355632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58170273 | AAACTAGAATTTCCT[A/G]TCCCGCCAAACTAAC | 55120 |
| rs186367016 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221490 | TCTTACAAACCCTAG[A/T]TGCTAAAATTTACCA | 55120 |
| rs186390423 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58219245 | GGACACAGGAGCCAA[C/T]TGAAAGAGCTCTCAA | 55120 |
| rs186442002 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242517 | ATCCTTCTTCCCTGA[C/G]GCGGGTCATTGGATC | 55120 |
| rs186464457 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58175402 | AAAATACTGGCAAAC[A/C]AAATCCAGCAGCACA | 55120 |
| rs186492083 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58168317 | AGCCAAAGCAGGGTG[G/T]GCTATCACCTCACTC | 55120 |
| rs186570463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239237 | TTACAAAAGGAGACT[C/G]TGACAGATGATACCT | 55120 |
| rs186593085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58205874 | TTTAAACCAAATTAT[A/G]AACAATAAAACTGCA | 55120 |
| rs186646688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232541 | TAACATTATATAGTC[A/G]TTTTCAGCTTACTTT | 55120 |
| rs186716710 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217227 | ATATACACACACACA[C/T]ACACACACACACACA | 55120 |
| rs186773134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169981 | TTAAAAAACACTCTT[C/T]AGGATGTTATCCAGG | 55120 |
| rs186783325 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58193326 | ACTACTGCCTAAATA[A/C/G]AAGCATTAATGGTAA | 55120 |
| rs186794482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180186 | TCAAGGATCTAGAAG[C/G]AGAAATACTGTTTGA | 55120 |
| rs186861967 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242936 | GGGCTCAGCAGTCTG[C/T]GTTTTAACAAGCTCT | 55120 |
| rs186875986 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58228705 | AATGATACAAGAAAA[A/G]AATAGTAATATTCAC | 55120 |
| rs186882366 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58211002 | CAAGCTGTCAGTGGA[A/T]CTACCATTCTGGGGT | 55120 |
| rs186888676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193466 | AAGAAAGGCAGCTGA[C/T]AGGTGACTAAGTCTA | 55120 |
| rs186895103 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58180561 | AGGGCCTGTCGGGGG[A/G]TGGGGGACTAGGTGA | 55120 |
| rs186903801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236293 | GAAAAGAGCAGAGAT[C/T]TCTCGTAGAAAACAG | 55120 |
| rs186903922 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58220066 | GAGAAAACATATAAA[A/G]TAAGATTACAGAGAC | 55120 |
| rs186942044 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58213553 | AAAACAAATGATTAA[A/G]TAACAGCAGCTAAAT | 55120 |
| rs186963865 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58182162 | AGGTAAGAAACCACA[A/G]AAATATTATCAGTAA | 55120 |
| rs186995304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164217 | TTTTTTGAAGGTACA[C/T]AGTGTAACTGCTTAA | 55120 |
| rs187009527 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58177825 | AAAAAACAAAAAAAA[A/C/T]CCAAATAGACCGCTA | 55120 |
| rs187026516 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58215138 | GTCAAAATAATATTT[A/C]TTTATTCCATCAATC | 55120 |
| rs187031955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58197271 | TATTAGGCTTTTTAT[C/T]TTTTTACTAATTTCT | 55120 |
| rs187037653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183191 | AAATATTTAAAATAA[A/G]AATGAACAGATAATA | 55120 |
| rs187063453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231735 | TATCAGTCAAAAGTT[C/G]GAAAAAAAGTTTTCT | 55120 |
| rs187131600 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58231023 | TTGCATCTAACCTAT[C/T]TCTTTGTAATCCTCA | 55120 |
| rs187147242 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58167623 | TTTTGAACAGAAAAA[A/T]GTATTCTTAATAAGA | 55120 |
| rs187152244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58196190 | CACGGATGGCCTATA[C/T]ACCAATTTTGGGTAA | 55120 |
| rs187189469 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58227460 | GAGACAGAAGGGAGA[C/T]GGTTTTCCCCTGGCG | 55120 |
| rs187210033 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | FANCL | GRCh38.p7 | 2:58192939 | AAAATAAAACATTTT[A/T]AAAAATCAATAGCTT | 55120 |
| rs187263940 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58213678 | CAGGAGTGTGAGACT[C/T]GCCTGGGCAATACAG | 55120 |
| rs187275051 | snp | A/T | 0.275197 | 0.248727 | intron-variant | FANCL | GRCh38.p7 | 2:58175029 | aaataaactagaaaa[A/T]ctagaagaaatggat | 55120 |
| rs187287819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187429 | GTGGGGTGGGGGGGA[C/T]GGGGAAGGGATAGCA | 55120 |
| rs187414095 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58210369 | CCAATAAAACCATCA[C/G]ATCTCATGACACTTA | 55120 |
| rs187420612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234916 | AAATTGGACAAAACA[C/T]ATGAAACAATGATTT | 55120 |
| rs187428526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58179468 | TTGACAAACATGACA[A/G]AAACAAGCAATGGGG | 55120 |
| rs187461749 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58240661 | AAACTCCATATGAGA[A/G]GCCACTGGAATCAGC | 55120 |
| rs187462715 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160931 | GTTACACACAGTTTA[C/T]CATGTATCAACTAGG | 55120 |
| rs187463029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224646 | GATCACAAAGAAATA[A/T]CAAAACTTTCCATTG | 55120 |
| rs187503529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236172 | AAAACATGAAAAAAG[C/G]TACACCAAGGTACAA | 55120 |
| rs187515235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58219932 | ACATAAAATCCCTAC[C/T]GCATATCTTAGGACT | 55120 |
| rs187584935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223031 | AACCAGGATAGGACA[C/T]TATCAAATTGAGATC | 55120 |
| rs187698956 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242677 | CATGCTTTGTCCAAC[C/T]GTACTTCCCCACAAC | 55120 |
| rs187710930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58186873 | CAGAATGAGATATCA[C/T]CTCACACCAGTTAGA | 55120 |
| rs187714952 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210866 | ATCATGCTGATACAA[C/G]AGTTGAGTTCCCATG | 55120 |
| rs187728710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233181 | TTTAACCTAACATTA[C/T]AGACATCCCACACAA | 55120 |
| rs187731671 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216420 | AGTCTGAATAGCCAA[C/G]GGCAAATGCAGCAGG | 55120 |
| rs187735136 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58173595 | AAACGCTGAGAGATT[C/T]TGTCACCACCAGGCC | 55120 |
| rs187739792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58240275 | AATTTTTAACCTCTA[C/T]TTTCTGTGATGGTCA | 55120 |
| rs187751009 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58198907 | TGTGGTGGGCGCCTG[C/T]AGTCCCAGCTACTTG | 55120 |
| rs187759416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58183973 | ACCTATAATTGTGGA[C/T]GGTACAAGAGACAAC | 55120 |
| rs187847368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240512 | TTCCCATACCTTGAT[A/T]TCTTCAACTAGAAAA | 55120 |
| rs187857723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207492 | TGGATTCTTGAATGT[C/G]CTTGTGAAGAGAGGC | 55120 |
| rs187872758 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58173280 | CAGATTAAAGAAATA[C/T]AGAGAATGCCACAAA | 55120 |
| rs187900573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202913 | GTCTTCATAGAAAAA[C/T]GGCTAATTTTACTAA | 55120 |
| rs187908443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58186537 | TGGTTATTGTAGTCA[A/G]TGGTAGCTATGTAAG | 55120 |
| rs187946112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170630 | GGAGATCCATCTCAC[C/G]TGCAAAGAAACACAC | 55120 |
| rs187980488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190183 | TCTGTCAAGCAATCC[A/G]TAAAGAACATATCAC | 55120 |
| rs187989722 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58203290 | CAGCTTTAGATATTA[A/C]TTTTCTCTTGTGGAA | 55120 |
| rs188001732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228247 | ATATTTAAGAGTTAC[C/T]ATTCCATTTCCTAGA | 55120 |
| rs188016555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171115 | TTTTAAAACTGATCA[C/T]AAAATTTGAAGTAAA | 55120 |
| rs188077775 | snp | C/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58173105 | AAGAATAACAAGAAA[C/T]GAACAAAGCCTCCAA | 55120 |
| rs188156953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186256 | AGTCAAATAATCAAA[A/G]AGCAAACATCAGAAT | 55120 |
| rs188161103 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169553 | GGACAGAGAATGAGT[A/C/T]TGACAAACTGACAGA | 55120 |
| rs188215817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239028 | ATATAATTAAATAAA[C/T]GAGAAAGCAGGCAAT | 55120 |
| rs188238175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209379 | AACCTAGAAAAACAT[C/G]ATTTTTTTTTTACTA | 55120 |
| rs188245711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233831 | AGTCAAGGAGCCAGT[C/T]CTGGGAAAGAATGCT | 55120 |
| rs188248196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58191512 | TTTATAGTACAATGT[A/G]TATGTAGTCACCTTC | 55120 |
| rs188252592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217675 | GTATGTACCCAATAA[C/T]ATGACTGCAAATAGA | 55120 |
| rs188258536 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58179025 | GAATCCAACTTACAA[C/G]GGATGTGAAGGACCT | 55120 |
| rs188306798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166081 | TGACAGTAGACTATA[C/T]ACCTGAGAAAGAATG | 55120 |
| rs188352625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229513 | GGGTCTGATTTTTTT[C/T]CCCTATCACCACCAT | 55120 |
| rs188366325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194146 | TATAAAGACCACTAT[C/T]TACTACACCACACTG | 55120 |
| rs188375806 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58168726 | GCTGCCAGCACAGCA[C/G]TCTGAAGTAGACCTG | 55120 |
| rs188386797 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58212069 | CCAATTTACTGTATT[A/C]GTCTGTTTTCATGCT | 55120 |
| rs188393218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194919 | CAAAGCCATGTCTAT[G/T]ATATCACAAAAAAAA | 55120 |
| rs188399431 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58181762 | TATGTCAGAAAATTT[G/T]TAATAAAACATTGGA | 55120 |
| rs188488574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230648 | GCCTTTTCAAACTGT[C/T]ACAACTCTCTCCATT | 55120 |
| rs188501884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215665 | CAAGAGAAGAAGGAT[A/C]TGGGCAAAGAGCCCA | 55120 |
| rs188503140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212907 | CTCAATATTATTTCC[A/G]TATTTCTTTCTAAGG | 55120 |
| rs188509398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170865 | ACAGAAGCAACCAGA[C/T]TCATAAAGCAAGTTC | 55120 |
| rs188511064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195884 | AAAGAGGCACATAGC[A/C]TGAAATCCAGCATTT | 55120 |
| rs188522273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58183464 | ACTGCTTTTATTACC[A/G]AACCTCAGTGAAGAG | 55120 |
| rs188637364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58211677 | CAAGTCACCTCTTCA[A/G]TGTTTTGCTGCTTAG | 55120 |
| rs188651766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206572 | ATCACAATGTTTAAA[A/G]TCATTTTTTAACATC | 55120 |
| rs188658186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181045 | TCCTACCTTAACCTG[G/T]CAATTCTACTCCAAA | 55120 |
| rs188673141 | snp | A/G | 0.00139149 | 0.0263402 | intron-variant, downstream-variant-500B, missense, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160083 | CTAGGCACATTTTAT[A/G]AGATGTGATTAACAA | 55120 |
| rs188681684 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FANCL | GRCh38.p7 | 2:58174115 | ATATGCACCCAATAC[A/G]GGAGCACCCAGATTC | 55120 |
| rs188783895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232799 | AAGTGAATGGGTAAG[C/T]AGTTTAAACTTTATA | 55120 |
| rs188793396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198459 | CAAAGTCCCATTTAT[A/G]TAAGAGATTTGGGTA | 55120 |
| rs188804548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164894 | TTCTCGTAATACCAC[A/G]TATGTGACATTCTTC | 55120 |
| rs188811886 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58178103 | GCAGTATTTAATAGC[C/T]TACTAACCAAAAAAA | 55120 |
| rs188885596 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58177311 | ACTATAAATCATGCT[G/T]CTATAAAGACACATG | 55120 |
| rs188886635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237559 | AATCAGGAAACTTAA[C/G]ATCAGAAAACTATCA | 55120 |
| rs188899170 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58220912 | ATACTATTGATAACG[A/G]TTAAGAAGTGATAAG | 55120 |
| rs188902839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203846 | GTTACATGTAGGATG[C/T]TACAAAATTAACACC | 55120 |
| rs188913422 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58187422 | GCCTGTCGTGGGGTG[G/T]GGGGGATGGGGAAGG | 55120 |
| rs188922810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58221877 | TAAACTGCTAAAACT[A/G]GAAATACATTAAGTT | 55120 |
| rs188935358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188897 | AAAGGTGAATGGCCA[A/G]TATGTGGCACATCCA | 55120 |
| rs188944918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160339 | TATTTCCTGAGCCAA[G/T]AGCAGACTATTAAGA | 55120 |
| rs188955556 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58174524 | GAAACTGAACAACCT[A/G]CTCCAGAATGACTAC | 55120 |
| rs189050230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208004 | TTTGAGGTTGCAGTG[A/C]GCTATGATGGCACCA | 55120 |
| rs189054485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190788 | TTAATACTGTCTCAG[C/T]GTCTCTACTATTTAC | 55120 |
| rs189062884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160941 | GTTTATCATGTATCA[A/G]CTAGGCCCTAAGGTG | 55120 |
| rs189121096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226132 | GTAGAAGAGGAAATA[A/T]GATTGGCAAAATGTT | 55120 |
| rs189137543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234943 | ATTTTCAGACATTAA[A/G]CAATAGGCAGCGAGG | 55120 |
| rs189145551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58218712 | GATAGTGCTCTGCAC[A/G]TATACTGCAACTGAA | 55120 |
| rs189147276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199886 | TCAGTACTCTGCTGG[G/T]TAAGTAAAAGGGAAG | 55120 |
| rs189155208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163624 | TTCACTGTATACCCA[C/T]GGAAAGATTAACCAA | 55120 |
| rs189178005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171816 | GGCACTGCCTCCCTC[A/G]GGAAGTGCAAAGGGT | 55120 |
| rs189251993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221293 | AATGTAATGTTTCAA[A/C]GTATCCACACTAAGA | 55120 |
| rs189267219 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58187571 | AAAGTATAATAATAA[A/T]AAAAAAAAAGTGTTG | 55120 |
| rs189389475 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241841 | AAGTTCAATCAGATA[C/T]ATTTGAGGCACACAC | 55120 |
| rs189401604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58237261 | TTTTAAAAATTTAAA[C/T]CATACAAGTTATATT | 55120 |
| rs189410042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58181823 | AATGATATAAATTAC[A/G]TATGAGTTATTTGTT | 55120 |
| rs189417967 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58203428 | AAAAAAAGTTGGACA[C/T]CCTGGTTTTCTTCAA | 55120 |
| rs189443589 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58184581 | GCATACATACAATAA[G/T]AAGAATAAGGAAATG | 55120 |
| rs189542705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58204789 | ATTTTCTTTCTGCAC[G/T]ATATATAGCTTCTGA | 55120 |
| rs189543073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230168 | TAGATTCTTTTCCAA[C/G]ATAGGTTAAATAAAA | 55120 |
| rs189619087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228267 | CATTTCCTAGAAATC[C/T]TTCATTCTTAAAATA | 55120 |
| rs189629843 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170386 | GAGCTCCTGAAGGAC[A/G]CGTGAAATATGCAAA | 55120 |
| rs189631621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210889 | TTCCCATGACCTTGG[A/G]GAGCTAGACCCCTGT | 55120 |
| rs189640075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58193395 | TTCTCTTCTTTTTTA[A/G]AATCAATATAGGCTG | 55120 |
| rs189641790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235002 | ATGTGAAAATGCCTA[A/G]AATTGTCTGGTTCTA | 55120 |
| rs189685315 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58220447 | CTAAATAAAAGCCTT[G/T]TAAGGAATATAAAGG | 55120 |
| rs189701196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187109 | TACTATAAAAACACA[C/T]GCACACATATGTTTA | 55120 |
| rs189765714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58231930 | TCAGAAATGTTTCTT[C/T]TGGGGCAAATGACTA | 55120 |
| rs189769724 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58213921 | CCAGGTAGTTGGGGA[C/G]AATTTATTAAAGGCT | 55120 |
| rs189783871 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197083 | CATCAAAATACCAAA[A/T]GCAAATTACAGGCTC | 55120 |
| rs189790032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183069 | CATTATTATAAGACA[C/T]ATAGTACTCATCCTA | 55120 |
| rs189996109 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169797 | TCAAGCGGAAGAAAG[C/G]ATATCAGAGATTTAA | 55120 |
| rs190060712 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187778 | AGAACGTGTGTATAC[A/G]TAAAACAACGTCCAT | 55120 |
| rs190080326 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58218154 | TAACATCAAAACTTA[C/T]GGGATCAAGCTAAAA | 55120 |
| rs190094001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184863 | AAAGTTAGGAAACAT[A/T]AAACAAGGTGAGAAT | 55120 |
| rs190127453 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58172332 | CTGACCCCTGAGCAG[C/G/T]CTAACTGGGAGGCAC | 55120 |
| rs190203433 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241408 | CCGCGGAGCGGAAAC[C/G]CCAGCCTTGGCGGGA | 55120 |
| rs190219773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208634 | AACAGGCAGACTGCT[C/T]CAAAAGACAGACTGA | 55120 |
| rs190236482 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58178634 | AATATCATACTGAAT[A/G]GGCAAAAGCTGGAAG | 55120 |
| rs190243101 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169021 | GCGGCTGTGGGCACA[A/G]CTTCAGCAGACTTAA | 55120 |
| rs190274914 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58232607 | ACAATCTATACAGAC[A/G]TAAGTGAAATACTTG | 55120 |
| rs190288050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58215246 | GCATCTCAACTTTTT[A/G]CTTGTCTTCCCTGTC | 55120 |
| rs190312929 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58234708 | CAACAGATTTTCAAA[A/G]TAAGAAAAAAGTCCA | 55120 |
| rs190335102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200609 | TTGGAGTAGATACAC[A/G]AAGTAAAGTATCTGT | 55120 |
| rs190377299 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58169091 | CCCACCACAACACTC[A/G]AGCTCTGCTAAGGGA | 55120 |
| rs190410522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162412 | GTCTGTCATTAATGA[C/T]GTCACTACTGAAGAC | 55120 |
| rs190421279 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58175437 | AAACGTTATCCACCA[G/T]GATCAAGTGGGCTTC | 55120 |
| rs190455830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225367 | TACCTCAAATTAACC[A/G]AACAACTGATGAGAA | 55120 |
| rs190476573 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190895 | CAAAAAGATGAGGGG[A/G]GAATATTTTCTAGCT | 55120 |
| rs190548194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239594 | AAAATTTGAAATATG[A/G]ACTCTATCTTAGATA | 55120 |
| rs190552344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221767 | TTTTACTTTGTAAGG[C/T]AATTTTTTATGATGA | 55120 |
| rs190562829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173122 | AACAAAGCCTCCAAG[A/G]AATATGGCACCATGT | 55120 |
| rs190565723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206279 | ATTCTTTTTCATTAA[C/T]CAGTTCATAATTCCT | 55120 |
| rs190572769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL | GRCh38.p7 | 2:58188669 | GGTCTCCAACTGCTG[A/G]GCTCAATCAATCTTC | 55120 |
| rs190687306 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242030 | CAGGAATGTTATCCA[C/T]CCCATCTTATTAAGA | 55120 |
| rs190693635 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58176475 | CTCAGAAATAACGCC[A/G]CATATCTACAACTAC | 55120 |
| rs190700938 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58186311 | GGCCATAAGTATGAT[C/T]GGTATATTTGGACCC | 55120 |
| rs190702997 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226909 | CTACATCTGAAAACT[A/C/G]TAAGAAATGAAGTAT | 55120 |
| rs190708947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210251 | CTCACAGTTCCATGT[A/G]GCTGGGGAAGGCTCA | 55120 |
| rs190713415 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58201278 | AAGCTCCATATCATA[G/T]AGGAATATTAACTGA | 55120 |
| rs190717178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192795 | AATCAGCTAACAGCC[A/G]AAAGTGTTTGCCCCT | 55120 |
| rs190720931 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58201895 | TTTATTTACTGTATA[C/T]TTAAAAAATCAAGTA | 55120 |
| rs190721868 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58185662 | CAGGGTAAGGACAGG[G/T]TTGGTTATTCTTGCT | 55120 |
| rs190777696 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58164997 | AGAATTTCAAAATAC[C/G]CTTGAACAACATATC | 55120 |
| rs190824662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172884 | GAAGAAGCTGAAAAC[C/T]TTGAAAAAAATTTAG | 55120 |
| rs190930442 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242682 | TTTGTCCAACCGTAC[G/T]TCCCCACAACTGTCC | 55120 |
| rs190961149 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219189 | ATATATATATATATA[A/T]ATATATATATATATA | 55120 |
| rs190976618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185859 | GGAGTCAGTAGTTTG[A/G]CTTGTACAGTGTTAT | 55120 |
| rs190981696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205945 | AAATATTTATGTAGT[C/T]GTAAAAAATTAAACT | 55120 |
| rs191050487 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58172696 | TGGGGAAAAAACAGA[A/C]CAGAAAAACTGGAAA | 55120 |
| rs191055541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240306 | TATGGTAATTCCACA[C/T]ATACTCAAAGACTAT | 55120 |
| rs191212968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180380 | TACACCATGGAATAC[A/T]ATGCAGCCATAAAAA | 55120 |
| rs191339144 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58168508 | CTGGGTTTCAAGCAC[A/C]AAACTGGGTGGTCAT | 55120 |
| rs191373985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239376 | ATTAGCTGAATTTAA[C/T]AGTGAGGAAATATCA | 55120 |
| rs191379452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171412 | ATAACGAAATGCCCA[A/C]ATGAGAAAGCAGAAA | 55120 |
| rs191380061 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183342 | TGAAAAAAAAATTAA[C/G]TATATGGGTGTAGGT | 55120 |
| rs191445475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233541 | ACCATATTAAGAATA[A/C]ATAAAACCACAAAAA | 55120 |
| rs191453402 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217179 | TTTTATATATATATA[C/T]ATATATATATATATA | 55120 |
| rs191457354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199092 | TATTATAACTGAAAA[C/T]GTATTACATATAAAT | 55120 |
| rs191467298 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58184404 | AGAAAAACTGCAATA[A/G]TCAATAAACTCTTGA | 55120 |
| rs191483351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167282 | TTTGAGGATATTGAC[A/G]GTATAATGTCTGTTC | 55120 |
| rs191484736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164277 | AAATGTCTTGATAAA[A/T]TCCATACACTGTAGA | 55120 |
| rs191494951 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58177830 | ACAAAAAAAACCCAA[A/G]TAGACCGCTAGCCAG | 55120 |
| rs191516320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231115 | AAGTTTTCCTCTTCT[C/G]TGGTCAATCCTTAGT | 55120 |
| rs191527291 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FANCL | GRCh38.p7 | 2:58196267 | AGGAGGGACAGAAAA[A/G]GGGGTCAGGTCTTAG | 55120 |
| rs191612614 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58197878 | TCAATGTCAAAAGTT[C/T]TAGCAATATAAAACA | 55120 |
| rs191613343 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170182 | ATCAGACTAACAGCA[C/G]ATCTCTCTGCAGAAA | 55120 |
| rs191617222 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170652 | GAAACACACAGGCTC[C/G]AAATAAAGGGATGGA | 55120 |
| rs191625343 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221522 | TCAAATTACAAAAGC[A/G]CTTATAATGTTATAT | 55120 |
| rs191626863 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58219508 | CTTCCAAAGAGTAAA[A/G]TGTGGAGAGAGAGAA | 55120 |
| rs191775068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213554 | AAACAAATGATTAAG[A/T]AACAGCAGCTAAATC | 55120 |
| rs191796408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58182849 | AGATGCAATAGAGTA[C/T]GCTGATTAAGATCAA | 55120 |
| rs191797058 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58179504 | ATTCCCTATTTATTA[A/C]ACGGTGTTGGGAAAA | 55120 |
| rs191854241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207829 | TCTGGGAAGCTGAGG[G/T]GAGGATTACTTGAGC | 55120 |
| rs191858496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190426 | ATAAGTAGGTACTTT[C/G]AATCTTATCCTTAGC | 55120 |
| rs191889783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233917 | ATTAGGAGGAAAAAG[A/G]AAAGTGGGAAACTTA | 55120 |
| rs191916616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235391 | TGTAAGAGCCATTAA[A/C]TAGAGTGCTCAGAAG | 55120 |
| rs191925781 | snp | G/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163483 | CATAGTAGGATGCCT[G/T]GGGTCTACCTCTATA | 55120 |
| rs191933765 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202676 | TAAAAGCATCATCTT[A/G]TCTACCTTGAAAAAG | 55120 |
| rs191944718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240904 | TTTACAAAAAAAAAA[C/T]TAAAAAACAGTCAAT | 55120 |
| rs191963330 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58224736 | TAAGTGAAATATAAC[A/C]AGTAGAACATAACAA | 55120 |
| rs191969664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179138 | GGAAGAATCAATATC[A/G]TGAAAATGGCCATAC | 55120 |
| rs191969898 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58208261 | TATTTAGAAGGAGTT[G/T]AGATATTATCACTAA | 55120 |
| rs191979160 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58190827 | ATATTTTCCAATTCT[A/G]TATCTATCTAATAAA | 55120 |
| rs192060383 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58174176 | GACTTAAGACTCCCA[A/C]ACAATAATAATGGGA | 55120 |
| rs192087780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58192997 | ATACAATTAAAAAGA[C/T]TGCATTAAAAATAAC | 55120 |
| rs192109695 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243321 | CCTAATCATTTAGCA[C/T]ATTTCCTGCTGCATC | 55120 |
| rs192112014 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203447 | GGTTTTCTTCAAATT[C/G]TCATGTTTCTCCAGT | 55120 |
| rs192115554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242520 | CTTCTTCCCTGAGGC[A/G]GGTCATTGGATCCTC | 55120 |
| rs192124283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58187371 | ACTGAACAATGAGAA[C/T]ACTTGGACACAGGGC | 55120 |
| rs192124647 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58228856 | AAACAGAGTAATAGA[C/T]CTTAATATTAGACTA | 55120 |
| rs192125918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210417 | AATATGGGGGAAACC[A/G]CCCTCCCACAACACA | 55120 |
| rs192128277 | snp | C/G/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58211226 | GTTCTGAAACCTCAG[C/G/T]TCTGGACTTCTGTGC | 55120 |
| rs192202693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236447 | TATGTATATTATAAA[A/C]CCTTTAAGCAACTAG | 55120 |
| rs192222066 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58203341 | TTTTAAAAAGGACAA[A/C]CACAATTGATCTTTT | 55120 |
| rs192233717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171032 | CAAGCAGACCTAATA[A/G]ACATCTACACAACTC | 55120 |
| rs192245237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164069 | AAGATTTCATTCACA[C/T]TGGCAATTGTTCATT | 55120 |
| rs192349864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173318 | TCGAGAAGAGCAACT[C/T]CAAGACACATAATTG | 55120 |
| rs192354907 | snp | C/T | 3.49534e-05 | 0.00418037 | intron-variant | FANCL | GRCh38.p7 | 2:58222063 | TAAAAGAAGAAAACC[C/T]GAATTAGCTGTGGAA | 55120 |
| rs192366364 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58169412 | AAAGTCAACAATATC[A/C]AAGACCAAACGTAGA | 55120 |
| rs192375262 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58189131 | GGGAGGGACAATAAT[C/G]AGGAAGGAGGTGACT | 55120 |
| rs192402660 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58173616 | CCACCAGGCCTGCCC[G/T]AAAAGAGCTCCTGAA | 55120 |
| rs192492756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167633 | AAAAATGTATTCTTA[A/G]TAAGAAAATAGCCAA | 55120 |
| rs192494792 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58227932 | GAGGAGGAGGAAGAG[A/G]AAAAAAAAGAGAAAG | 55120 |
| rs192623562 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58220169 | TCCGAGGCTGTAATT[C/T]TTATCAAGACCAGGA | 55120 |
| rs192639542 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58186893 | CACCAGTTAGAATGG[C/T]AATCATTAAAAAGTC | 55120 |
| rs192652413 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58236214 | GTGACTGAAACCAAT[A/G]ACCAAAAAGAAAAAT | 55120 |
| rs192665141 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58177357 | TGCAGCACTATTCAC[A/C]ACAGCAAAGACTTGG | 55120 |
| rs192670068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219972 | AACATCCTTTAATCC[A/G]AGTCAGTGGCATCCT | 55120 |
| rs192674486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203163 | GACTTATCACATATG[A/G]ATCTTAAAATTAGAC | 55120 |
| rs192684703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186605 | AACCAGAATGCAAGA[A/G]CATTTTTTTCCGGCT | 55120 |
| rs192738544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206818 | TTCAGATTAATATCA[C/G]CATGGCCATTTAAAA | 55120 |
| rs192754138 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159638 | ATGTTTATTATTATC[A/G]CATCATCATACCTGT | 55120 |
| rs192773819 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58217926 | GGAAATAGAACACAT[A/T]CCAAAATTGACAAGG | 55120 |
| rs192848111 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58232938 | TCAAAAAACAATTAC[A/C/T]ATGTGGAATTTTAAC | 55120 |
| rs192860123 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58198501 | TGGTATTTACAGAGG[A/G]CCCAAGAAATAATCC | 55120 |
| rs192906462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220873 | ATAGGGCAATCTAAA[C/T]GGAAATAATAAATGA | 55120 |
| rs192923552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58193863 | CATATACAGTACATA[C/T]GAACTGAGGCAAAGG | 55120 |
| rs192951077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178388 | CTTATCTACCACGAT[A/C]AAGTTGGTTTCAACC | 55120 |
| rs192991624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223197 | GAATATCAATATGGA[C/T]TTAATTAGAGGGTAA | 55120 |
| rs193062013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58216209 | ACAGGAAGGGCAGCA[A/G]TCAGAGGTAGACTGA | 55120 |
| rs193138435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211970 | TGAGCCTTCCAAACC[A/G]TTCCAACCTCTGCCT | 55120 |
| rs193143949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181139 | AAGCACCAAAAACTG[C/G]TAACAGTCCAGATGT | 55120 |
| rs193167564 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58180599 | TATTAGGAGAAATAC[A/C]TAATGTAGATGTCGG | 55120 |
| rs193176786 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164901 | AATACCACGTATGTG[A/T]CATTCTTCCCCCAGA | 55120 |
| rs193294003 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58194570 | GCACTTTGTGCTTCT[G/T]TGGCACATATCATGG | 55120 |
| rs199520335 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58228870 | ATCTTAATATTAGAC[-/T]ACATAAACCATTTTT | 55120 |
| rs199527629 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58182066 | TATGATAAGCATTCT[C/G]AATCAGAGAATCTCA | 55120 |
| rs199550601 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173357 | ACCAAAGTTGAAATG[A/C]AGGAAAAAATGTTAA | 55120 |
| rs199564543 | snp | C/T | 0.000247103 | 0.0111126 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165793 | CCCAGGTCTTCTCAT[C/T]GATTTCATCCATAAC | 55120 |
| rs199574967 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223429 | GAAATATTAATTATT[-/G]CTATTCACAAAAATT | 55120 |
| rs199602133 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58217791 | CTCAGGACAAGCGGA[A/C]AAAAAAAAAAAATAA | 55120 |
| rs199660431 | snp | A/T | | | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165817 | CCATAACATCCCAGA[A/T]TGCCTTTAGTGATTC | 55120 |
| rs199661008 | snp | C/G | 3.91183e-05 | 0.0044224 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241353 | AAAAGCTCTAGACCT[C/G]CTGGGTCCTGCACAT | 55120 |
| rs199686678 | in-del | -/AAG | 0.0170251 | 0.090679 | intron-variant | FANCL | GRCh38.p7 | 2:58164596 | GCCTGGAGGAGAAAA[-/AAG]AAGCTAAAAGGTAAA | 55120 |
| rs199707945 | in-del | -/ATT | | | intron-variant | FANCL | GRCh38.p7 | 2:58206325 | ATTGCATGTAGGCAG[-/ATT]ATTTAGAAACATGGA | 55120 |
| rs199732201 | snp | C/T | 0.00199806 | 0.0315443 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159620 | GTGAAGAGACAAACG[C/T]AGATGTTTATTATTA | 55120 |
| rs199772991 | snp | A/T | 0.0667028 | 0.170006 | intron-variant | FANCL | GRCh38.p7 | 2:58222327 | GAGATAAAAAAAAAA[A/T]TTTTATTAAATTCAT | 55120 |
| rs199852217 | in-del | -/ATATCCTTTAA | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58194005 | GCTATGTAATAGGAC[-/ATATCCTTTAA]TGACTCCTTTAATTA | 55120 |
| rs199860158 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58177037 | ATGAAAAAATGCTCA[C/T]CATCACTGGCCATCA | 55120 |
| rs199875654 | snp | A/G | 0.00199799 | 0.0315437 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162894 | ATAGCACGAGCTGGA[A/G]AATCAATTTCTAAAA | 55120 |
| rs199878008 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58233335 | TTTTAAAAGGTCAAA[-/T]TAACATGTCACATGC | 55120 |
| rs199889756 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199829 | ATTTGACAAATTATT[A/T]AAAGAAGTTTTAGGC | 55120 |
| rs199948753 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169583 | AAGTAGGCTTCAGAA[A/G]GTGGGTAATAACAAA | 55120 |
| rs199954173 | snp | A/G | 0.000291519 | 0.0120696 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159311 | ACTTGGATAACTCAC[A/G]TCTAACAAACTAAAC | 55120 |
| rs199966372 | snp | A/G | 9.91277e-05 | 0.00703946 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198610 | TGAGGTGTCCAGGAG[A/G]CACAAAATGGAACAG | 55120 |
| rs199988534 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58224929 | CACTGAAAAAACCTA[A/C]AAGTAACAGCAATGC | 55120 |
| rs200014581 | snp | C/T | 0.103438 | 0.202533 | intron-variant | FANCL | GRCh38.p7 | 2:58176950 | AAAAAAACAAACAAC[C/T]CCATCAAAAAGTGGG | 55120 |
| rs200072385 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58205890 | AACAATAAAACTGCA[G/T]TAAAAATGGTAATTA | 55120 |
| rs200106687 | in-del | -/ACTT | 0.0170251 | 0.090679 | intron-variant | FANCL | GRCh38.p7 | 2:58182684 | AAGAATGCAATCCTC[-/ACTT]ACATCACATCAGGTT | 55120 |
| rs200106971 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213716 | TTGTCTCTTAAAAAA[A/G]AAAAAAAAAAAAAAA | 55120 |
| rs200132675 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176030 | AACTCCCATTCACAA[C/T]TGCTTCAAAGAGAAC | 55120 |
| rs200244869 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172435 | CAGACAGCAGCATTC[A/G]TGGTTCAAGAAAATC | 55120 |
| rs200306031 | snp | C/T | 1.65941e-05 | 0.00288041 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229833 | TGTACTATTCGATGG[C/T]ATCCACTAAGTATTG | 55120 |
| rs200310294 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58194009 | ATGTAATAGGACTGA[-/C]TCCTTTAATTACAAA | 55120 |
| rs200323182 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167985 | CCAAATTGAAAAAAA[-/T]AAATTATTTCTAAAT | 55120 |
| rs200325071 | in-del | -/A | 0.142873 | 0.225885 | intron-variant | FANCL | GRCh38.p7 | 2:58221907 | TAAAATATATAAAAC[-/A]AAGGCATTTAAAACA | 55120 |
| rs200334210 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | FANCL | GRCh38.p7 | 2:58192840 | ATGAAGGCTATGCTG[-/T]TTTTTTCTAAAAAGA | 55120 |
| rs200355042 | snp | C/G | 1.65501e-05 | 0.00287659 | missense, stop-gained, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241230 | TACCTGAGCCGAGAT[C/G]AATCCCTCATACACG | 55120 |
| rs200388525 | in-del | -/ATAA | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58203612 | TCCTATAAGGGATCT[-/ATAA]ATAGAGGCATAACCT | 55120 |
| rs200412376 | snp | C/T | 3.36287e-05 | 0.00410039 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159797 | ACATTTTTAAGGTAA[C/T]TGGCTTTAAAAAGAG | 55120 |
| rs200428034 | in-del | -/AAACAGTCAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58240909 | AAAAAAAAAATTAAA[-/AAACAGTCAA]TTGCGGGACACTGAA | 55120 |
| rs200441282 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58213717 | AAAAAAAAAAAAAAA[-/AA]GAGAGGGAAAAAAAG | 55120 |
| rs200467879 | in-del | -/AACT | 0.0414363 | 0.137845 | intron-variant | FANCL | GRCh38.p7 | 2:58170475 | TGAAGAAACTGCATC[-/AACT]AACTAACAAAATAAC | 55120 |
| rs200544068 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215719 | CAAAAAAAAAAAAAA[C/T]CATCATTTCCGCCAA | 55120 |
| rs200559825 | snp | A/C/G | 0.000318081 | 0.0126075 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241293 | GCACTGGCGCAACAG[A/C/G]CTCGCTTCCGTCACC | 55120 |
| rs200560137 | in-del | -/T | 0.160043 | 0.233254 | intron-variant | FANCL | GRCh38.p7 | 2:58223008 | ATATCAATTTTTTTT[-/T]AACCAGGATAGGACA | 55120 |
| rs200614051 | in-del | -/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162497 | CTACTTATACACAGA[-/T]TTTTTTTTTTAACCA | 55120 |
| rs200645448 | in-del | -/A/AA | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58194936 | ATCACAAAAAAAAAA[-/A/AA]GAAAAATAAAGATCT | 55120 |
| rs200652916 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174710 | CAAAATTGACACCCT[A/G]ACATCACAATTAAAA | 55120 |
| rs200662163 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58236050 | ACAGAAAAGGAGGAA[A/C]AAAAAAAAAAAAAGA | 55120 |
| rs200679501 | snp | A/G | 0.000446071 | 0.0149277 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165869 | ATAAATGCTTATTAA[A/G]GAGCTCTGTGAAAAA | 55120 |
| rs200778219 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234088 | CAAACAGCCAAAACG[C/T]CCATGAATACAAAGA | 55120 |
| rs200819615 | snp | C/T | 8.27424e-05 | 0.00643151 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161573 | CTGAGAATTATCACA[C/T]ACTTGATCAGGAATG | 55120 |
| rs200849840 | snp | A/G | 0.000133558 | 0.00817076 | intron-variant | FANCL | GRCh38.p7 | 2:58232047 | TTATAACTAAACACC[A/G]TATCACCTTGCATTC | 55120 |
| rs200861962 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176913 | ATCCAGAATCTACAA[A/T]GAACTCAAACAAATT | 55120 |
| rs200862445 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58233562 | ACCACAAAAATCCCA[-/T]GTTTTCAGCCAGAAG | 55120 |
| rs200895973 | snp | A/G | 0.000265204 | 0.0115122 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162997 | TTTGTAAAATCACCA[A/G]AAAGTAAAAATTATA | 55120 |
| rs201046109 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206317 | AAAGAAATATTGCAT[A/G]TAGGCAGATTATTTA | 55120 |
| rs201084086 | snp | A/C | 9.94349e-05 | 0.00705036 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198641 | GAAAATCCACAAAAT[A/C]ATCTGGTGATTCTGC | 55120 |
| rs201154888 | in-del | -/A/AAAAAAATAAA | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58206294 | CAGTTCATAATTCCT[-/A/AAAAAAATAAA]AAAAAATAAAGAAAT | 55120 |
| rs201239590 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159538 | TACACTTCCACAGTC[A/G]GCACGGGGATCACAG | 55120 |
| rs201251765 | snp | A/G/T | 0.00166216 | 0.0287809 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161488 | CTATGTTGTGTTAGC[A/G/T]GAAAAAAGTCTTGAC | 55120 |
| rs201256168 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58215704 | GCTGCTATTAAGTGG[A/C]AAAAAAAAAAAAAAG | 55120 |
| rs201266814 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217215 | ATATATATATATATA[C/T]ACACACACACACACA | 55120 |
| rs201297014 | in-del | -/GC | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58198044 | TGTGTGTGTGTGTGT[-/GC]GCGTGTGTGTGTGTG | 55120 |
| rs201356389 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58177526 | CTCAGTAAACTATCG[C/T]AAGAACAAAAAACCA | 55120 |
| rs201368676 | in-del | -/A | 0.0352966 | 0.128072 | intron-variant | FANCL | GRCh38.p7 | 2:58183208 | ATGAACAGATAATAG[-/A]AAAAAATGAATAAAG | 55120 |
| rs201404515 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176929 | GAACTCAAACAAATT[G/T]ACAAGAAAAAAACAA | 55120 |
| rs201405464 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163332 | TCTCAGACAAAAAAT[-/A]AAAAACTACCATTAA | 55120 |
| rs201410058 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165828 | CAGAATGCCTTTAGT[A/G]ATTCTATTGCTGCCA | 55120 |
| rs201433154 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183629 | TATATTTTAAAAATC[C/T]TCTTTTATGACAATG | 55120 |
| rs201503665 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58173773 | AATGACAGGATCAAA[C/T]TCACACATAACAATA | 55120 |
| rs201513341 | in-del | -/T | 0.0630245 | 0.165952 | intron-variant | FANCL | GRCh38.p7 | 2:58228124 | TAATTGTGATTTTTG[-/T]CCTCTCACAACTAAT | 55120 |
| rs201570047 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171232 | CTCACTCAAAACTGC[A/T]CAACTACATAGAAAC | 55120 |
| rs201600562 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199823 | TCTTTCATTTGACAA[A/T]TTATTAAAAGAAGTT | 55120 |
| rs201610023 | snp | A/G | 1.6525e-05 | 0.00287441 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159469 | TATGAGCCTCATCAA[A/G]ATTTTACCAGTCCAG | 55120 |
| rs201644508 | in-del | -/ATGAG | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58180898 | AGAGTACTAATATTA[-/ATGAG]ATAACATTAAAATAA | 55120 |
| rs201689276 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205365 | TCTTAGAAAACAAAA[C/G]TATTCTAGAAAGTGT | 55120 |
| rs201708705 | snp | C/G/T | 9.9486e-05 | 0.00705217 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241275 | CTGGGGCAGAAGCAG[C/G/T]GGGCACTGGCGCAAC | 55120 |
| rs201729929 | in-del | -/TTG | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58193260 | TTTTTAAATGAAACT[-/TTG]TTAAGTGACAAGCAT | 55120 |
| rs201733792 | snp | A/G | 0.000182692 | 0.00955577 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161507 | AAAAGTCTTGACAAT[A/G]TTTTTATTTTTTACC | 55120 |
| rs201749725 | in-del | -/AAAC | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163200 | ATGTATTATGTTAAA[-/AAAC]AAAATTATACAGTTC | 55120 |
| rs201782544 | in-del | -/TTACT | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58164690 | ATCATAACCTGATAA[-/TTACT]TTAATGGGGCCACGA | 55120 |
| rs201828459 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169558 | GAGAATGAGTTTGAC[A/G]AACTGACAGAAGTAG | 55120 |
| rs201835070 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58175862 | CTGTTTGCAGACGAC[A/C]TGATTGTATATCTAG | 55120 |
| rs201860343 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58236473 | ACTAGTTAAAAAAAA[A/C]ACACACACACACACA | 55120 |
| rs201863300 | snp | A/C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187568 | CTTAAAGTATAATAA[A/C/T]AAAAAAAAAAAAGTG | 55120 |
| rs201875132 | snp | C/T | 0.000202494 | 0.0100601 | intron-variant | FANCL | GRCh38.p7 | 2:58232123 | CTTCCCTGTGGAAAA[C/T]ATTGAAAAGGATCAC | 55120 |
| rs201914378 | snp | G/T | 0.000917153 | 0.0213948 | intron-variant | FANCL | GRCh38.p7 | 2:58229778 | TAGTAATTTCTTATC[G/T]TCACTGAAAACATAA | 55120 |
| rs201953385 | in-del | -/AC | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58232952 | CCATGTGGAATTTTA[-/AC]ACAGTCTCCCTCAAA | 55120 |
| rs201977980 | in-del | -/TA | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58198417 | AGATAACTTAAAGTA[-/TA]CAGAAGAGTGTGCAC | 55120 |
| rs202063255 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190469 | GTACTATTCAAAAAG[A/G]AAAAAAAAAAAAAAA | 55120 |
| rs202137980 | in-del | -/GCAGTGTTCA | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58205772 | ACAGCTGGCAAAAAT[-/GCAGTGTTCA]GGATAGAGAGTATGA | 55120 |
| rs202162281 | snp | C/T | 9.92819e-05 | 0.00704493 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241258 | ACGGTTTTCGACCGG[C/T]TCTGGGGCAGAAGCA | 55120 |
| rs202191193 | snp | A/G | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158889 | CAGTTTTCTTTGGCT[A/G]TGTACAGCCTCATCC | 55120 |
| rs202210053 | snp | C/T | 8.24137e-05 | 0.00641873 | intron-variant | FANCL | GRCh38.p7 | 2:58165689 | ATACAAAATAAAACA[C/T]CTAAAAACAAACCCT | 55120 |
| rs202212067 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58202388 | TAACTTTTTTTTCCT[-/A]AAAAAAAAAATTATC | 55120 |
| rs367625287 | snp | A/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163474 | CTCAGGAAGCATAGT[A/T]GGATGCCTGGGGTCT | 55120 |
| rs367645171 | in-del | -/GC | | | intron-variant | FANCL | GRCh38.p7 | 2:58198045 | TGTGTGTGTGTGTGT[-/GC]GTGTGTGTGTGTGTA | 55120 |
| rs367669814 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239238 | TACAAAAGGAGACTC[C/T]GACAGATGATACCTT | 55120 |
| rs367684519 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199427 | ACAAACATGAATACA[C/T]ATAGCTGTCAATTTA | 55120 |
| rs367689766 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219277 | GGCCAAAGCTAGAAC[A/G]AATTGAGCAAGAAAA | 55120 |
| rs367703311 | snp | A/T | 0.000385849 | 0.0138844 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241339 | CCGGAGAAACACAGA[A/T]AAGCTCTAGACCTGC | 55120 |
| rs367776591 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58234106 | ATGAATACAAAGATA[A/C]TGTCTTCATCAATGC | 55120 |
| rs367789171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175858 | GTCCCTGTTTGCAGA[C/T]GACATGATTGTATAT | 55120 |
| rs367803579 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214989 | TCAGATCCACTGAGG[C/T]AGGCTGCCTCAAACT | 55120 |
| rs367826319 | snp | C/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163383 | ATTTAACAATGCTAG[C/G]CAAGGATTTTATGAC | 55120 |
| rs367876383 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182305 | CCTTTATACTGGGAC[A/T]TTTAAAAGTTTCTCA | 55120 |
| rs367879242 | snp | A/G | 3.36417e-05 | 0.00410119 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222035 | TGTCTATTCTTTAAG[A/G]CAACTTCCTGTTTAA | 55120 |
| rs367892841 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58177898 | ACAATAAAAAAATGA[G/T]GAAGGGGATATCGCC | 55120 |
| rs367894688 | snp | C/T | 3.33389e-05 | 0.00408269 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159697 | TTTTTTCTCTGAAGA[C/T]GATACCAAAATTCCT | 55120 |
| rs367932442 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168812 | GTGGTTTACCCCTCA[C/T]AGTGTATACAATGCC | 55120 |
| rs368003896 | in-del | -/GAGAA | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58173305 | CACAAAGATACTCTC[-/GAGAA]GAGCAACTCCAAGAC | 55120 |
| rs368052572 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226278 | GGATAAACTGAATAA[C/T]CAAGTATTTTATGCA | 55120 |
| rs368107475 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216278 | GCCCTTTGCCAATCT[A/G]TTCCCAGTCTATCTT | 55120 |
| rs368119259 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159183 | TAAACTCTTAAAAAG[C/T]GTAAATCTTTAAGAT | 55120 |
| rs368125495 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58176575 | GAAAACTGGCTAGCT[A/G]TATGTAGGAAGCTGA | 55120 |
| rs368257506 | in-del | -/ACACACACAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58217216 | TATATATATATATAT[-/ACACACACAC]ACACACACACACACA | 55120 |
| rs368275397 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58175474 | GGGATGCAAGGCTGG[C/T]TCAATATACGCAAAT | 55120 |
| rs368279793 | snp | A/G | 1.65146e-05 | 0.0028735 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159544 | TCCACAGTCAGCACG[A/G]GGATCACAGACTTAG | 55120 |
| rs368300021 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | FANCL | GRCh38.p7 | 2:58204269 | ATCACACCGGGGAGA[A/G]CTGGAGAGGGGAACT | 55120 |
| rs368329002 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192494 | AATAAAAACGAGGGT[A/G]ACAAAGGAAAATTAA | 55120 |
| rs368331490 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58219541 | AAACAGTAACTTTAC[C/G]GTGCAGAAACCCGAC | 55120 |
| rs368338920 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200571 | ATGTAGATAAAATAA[A/G]ACTAATGAAATGTTT | 55120 |
| rs368369905 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58210700 | CTAGATACAACAGGG[A/G]TATAGGCATTCGATA | 55120 |
| rs368384315 | snp | A/G | 0.000205356 | 0.0101309 | intron-variant | FANCL | GRCh38.p7 | 2:58241178 | CGCAGCTACGCTGCA[A/G]GAGGCTCTCTTAGCT | 55120 |
| rs368409823 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172803 | AATGACTTTGACGAG[C/T]TGAGAGAAGAAGGCT | 55120 |
| rs368440130 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214095 | CCTGAGAAATTAAAT[A/C]AGAATACATGAAGCA | 55120 |
| rs368443564 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181122 | ACAGCAGCTACATTC[A/G]TAAGCACCAAAAACT | 55120 |
| rs368471530 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58227540 | CCACGTCATTCTGCC[A/G]GTCAATGGCCTGCCG | 55120 |
| rs368585288 | in-del | -/TTAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58182686 | GAATGCAATCCTCAC[-/TTAC]ATCACATCAGGTTAT | 55120 |
| rs368604691 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200266 | TTATCTCAAAGTAAA[C/T]GTAGACAGAGACCTC | 55120 |
| rs368688452 | snp | A/C/G | 0.000492177 | 0.0156797 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241348 | CACAGAAAAGCTCTA[A/C/G]ACCTGCTGGGTCCTG | 55120 |
| rs368689742 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232336 | AGTTACTGGGAAATC[A/G]AAACACTCAGATAAG | 55120 |
| rs368750557 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58227956 | GAGAAAGAAGAGGTA[G/T]AGGAGTGATGTGAGT | 55120 |
| rs368756935 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211340 | CCTTTTCAGCCACAG[C/T]TGGAGCAGCTGGGAT | 55120 |
| rs368838149 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180860 | ATCAAAAAAGAAATC[A/G]AAACTTTTCAGAAAA | 55120 |
| rs368843119 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240773 | AAGGGCCAAAATAAG[A/G]TTTTCTTCCCAAATG | 55120 |
| rs368900762 | snp | A/G | 6.59e-05 | 0.00573983 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165804 | TCATCGATTTCATCC[A/G]TAACATCCCAGAATG | 55120 |
| rs368922000 | in-del | -/A | 0.0655868 | 0.168795 | intron-variant | FANCL | GRCh38.p7 | 2:58227932 | GAGGAGGAGGAAGAG[-/A]AAAAAAAAGAGAAAG | 55120 |
| rs368986645 | snp | A/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159719 | AAAATTCCTTTTGAT[A/T]ATTTTTTAAGTTTCC | 55120 |
| rs368988322 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241545 | AAGATTGCCCTCAAG[C/T]CCACAGGACTGACTG | 55120 |
| rs369011323 | snp | A/G | 0.193653 | 0.243567 | intron-variant | FANCL | GRCh38.p7 | 2:58177530 | GTAAACTATCGCAAG[A/G]ACAAAAAACCAAACA | 55120 |
| rs369016129 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58171011 | GAGTTGAACTCAGCT[C/G]TGGACCAAGCAGACC | 55120 |
| rs369041049 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218035 | TTAAACTGGAACTCA[A/T]TAACCCAAAAATCTC | 55120 |
| rs369048526 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | FANCL | GRCh38.p7 | 2:58226788 | GTGCTGCATTCTCTA[G/T]ATCAAAATATTTCCA | 55120 |
| rs369095757 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | FANCL | GRCh38.p7 | 2:58229904 | AGACAAAATGGTTTA[C/T]TCATTGTTCAGAATT | 55120 |
| rs369115051 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169364 | ATAGCATCAACATCA[A/G]CAAAAAGGACATCCA | 55120 |
| rs369127734 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194883 | CATAAGGAAAATTAC[C/T]CATTTTTAATATGGA | 55120 |
| rs369165797 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160656 | TGATTATAAGCATGA[A/G]CCAGTGAATTTTTAA | 55120 |
| rs369184967 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241644 | ACTGTTACAACTTTG[A/G]TGTTGCATTTCCTCC | 55120 |
| rs369204341 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194959 | AAAGATCTTCCAAGT[C/T]TAAAGTCCAGAAACA | 55120 |
| rs369256880 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241488 | GCCAAGTGGCGCTCT[A/G]CGGGAGGCGACATCA | 55120 |
| rs369259658 | snp | C/G | 1.66576e-05 | 0.00288592 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162845 | TACTGTCTGGAATAT[C/G]AAAACACTGATAAAA | 55120 |
| rs369293352 | in-del | -/A | | | | | GRCh38.p7 | 2:58243590 | TGACCACTTGCCAAA[-/A]GCAGTTGGCTCCTTG | 55120 |
| rs369309959 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178275 | AATCTGGAGGAGGCA[C/T]AACAGAAAAAGAAAA | 55120 |
| rs369327529 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58241078 | CTTCTCAAACCTTTA[A/G]TCTCCCAAGAGCCGT | 55120 |
| rs369374140 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161979 | CAAAGCTATTGTAGG[A/G]TGTTTCCTTTTCCAC | 55120 |
| rs369378431 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58234597 | ATTTAAAAATATAAT[C/G]CAAGTACACTTCCTG | 55120 |
| rs369423797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171637 | GGAGCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 55120 |
| rs369447345 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216937 | TTTCCCATTTCCTTT[G/T]ATGTTATTTTATTAC | 55120 |
| rs369455565 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58194056 | AGATTATCAGCCAGA[C/G]GCTTTATCATTAGTT | 55120 |
| rs369523860 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159902 | GTGTCATAGTACAGT[C/T]TGGAAAACACTTCTG | 55120 |
| rs369534313 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58176862 | TACAAAATGGGAGAA[A/C]ATTTTCGCAACCTAC | 55120 |
| rs369604375 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58184511 | TCCAAAAATTACAAC[C/G]AGAACTTTGCAACTG | 55120 |
| rs369662044 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171767 | GCGCAAGACAGTGGG[C/T]GCAGTGCACCATGCG | 55120 |
| rs369699068 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221678 | ATACAGTTGTATGTT[C/T]AGTGAAAGTATCTAT | 55120 |
| rs369702659 | snp | A/G | 1.80794e-05 | 0.00300656 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163110 | ATTTAATAATTGCAT[A/G]CTCTACTCTTGGTTT | 55120 |
| rs369748775 | snp | A/G | | | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159360 | ATAGGAAAGCACAAG[A/G]AGAAGACAGAAATAT | 55120 |
| rs369752377 | snp | C/T | 0.000234098 | 0.0108164 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159750 | AGCTCTTCACCGAAA[C/T]GTTGTATTCTTATTT | 55120 |
| rs369755920 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190944 | TAGTGATGCTAGGAG[G/T]TCATATTTGAATTAA | 55120 |
| rs369756342 | snp | C/T | 0.000297162 | 0.0121858 | intron-variant | FANCL | GRCh38.p7 | 2:58204118 | ACAATAACAGTTTAA[C/T]GAGGCACATACCTTT | 55120 |
| rs369845485 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189803 | AGTGCCAGAATGTGA[G/T]CTTTTGTGCTATGAT | 55120 |
| rs369876807 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204165 | TGATTAAATGCTCTC[C/T]ACCAGAAGCATCTTC | 55120 |
| rs370066647 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191481 | GTATTTCTCTCAACA[A/T]CTCTTATCTCTGTTA | 55120 |
| rs370088083 | in-del | -/TTTG | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58206870 | CTGCTTCCTGGTCAC[-/TTTG]TTTGGGGCACAGAAA | 55120 |
| rs370100534 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230095 | CAGTAAATGACATGC[A/G]AACAGTACATCTTGT | 55120 |
| rs370104694 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58174501 | ACTCAAAACCGCTCA[A/T]CTACATGGAAACTGA | 55120 |
| rs370106620 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213498 | AATCCATGCACACCA[C/T]TTCTCTTCTGCTAAA | 55120 |
| rs370127908 | in-del | -/ATT | | | intron-variant | FANCL | GRCh38.p7 | 2:58165665 | GTCATTGTTAGATTT[-/ATT]TTCATAATACAAAAT | 55120 |
| rs370169018 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58220374 | GCCCACTCAGTCAAA[C/T]TTTAGTGGTTAAAAC | 55120 |
| rs370192898 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58168465 | CGCAGATCAGGAGAT[G/T]CCCTCTGGTGCCTAT | 55120 |
| rs370202006 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58181842 | GAGTTATTTGTTATA[A/C]CTGAGAAAGCTGACC | 55120 |
| rs370217096 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180382 | CACCATGGAATACTA[C/T]GCAGCCATAAAAAAG | 55120 |
| rs370244462 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213561 | TGATTAAGTAACAGC[A/T]GCTAAATCGAAAGTC | 55120 |
| rs370283793 | snp | G/T | 1.65463e-05 | 0.00287626 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160149 | ATATGATGTTAAAAC[G/T]CTGTCTACTAGTTAG | 55120 |
| rs370362904 | snp | A/T | 5.46961e-05 | 0.00522925 | intron-variant | FANCL | GRCh38.p7 | 2:58222089 | TGGAACGCAAGACAA[A/T]GAACTGTTAATACCT | 55120 |
| rs370392756 | snp | C/G | 8.35429e-05 | 0.00646254 | intron-variant | FANCL | GRCh38.p7 | 2:58232045 | GTTTATAACTAAACA[C/G]CATATCACCTTGCAT | 55120 |
| rs370409722 | snp | C/T | 5.00171e-05 | 0.0050006 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241287 | CAGGGGGCACTGGCG[C/T]AACAGGCTCGCTTCC | 55120 |
| rs370412981 | snp | A/C | 0.119281 | 0.213102 | intron-variant | FANCL | GRCh38.p7 | 2:58175242 | CCTTCTGAAACTATT[A/C]CAATCAATAGAAAAA | 55120 |
| rs370449029 | snp | C/G/T | 3.67493e-05 | 0.00428644 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163532 | CCTAGAATGAAACAA[C/G/T]ATTAAATCTTTTAGA | 55120 |
| rs370465804 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190468 | TGTACTATTCAAAAA[-/G]AAAAAAAAAAAAAAA | 55120 |
| rs370472584 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198854 | CTATACGGTGAAACC[C/T]CGCCTCTACTAAAAA | 55120 |
| rs370515140 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205889 | AAACAATAAAACTGC[A/G]TTAAAAATGGTAATT | 55120 |
| rs370558500 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170778 | AAAAGAGACAAAGAA[C/G]GGCATTACATAATGG | 55120 |
| rs370564291 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224053 | GGATTTCATTTTTAT[G/T]CAGAAATTGAATAAA | 55120 |
| rs370624007 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209818 | ATTTAGTATGAACAA[G/T]GATCTCCATTTCCCC | 55120 |
| rs370652481 | in-del | -/TTTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58206329 | CATGTAGGCAGATTA[-/TTTA]GAAACATGGAAGTTG | 55120 |
| rs370670536 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58172907 | AAATTTAGACGAATG[C/G]ATAACTAGAATAACC | 55120 |
| rs370670595 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218439 | CACAAAAAACTCATG[C/T]GGAAAGAAAAAGGCA | 55120 |
| rs370675563 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229953 | TAACACAAACATGCA[C/T]GTACATACAAAAGAA | 55120 |
| rs370676351 | snp | A/C/G/T | 0.000118268 | 0.00768917 | intron-variant | FANCL | GRCh38.p7 | 2:58232029 | AAATGCAAAAATGCA[A/C/G/T]GTTTATAACTAAACA | 55120 |
| rs370695836 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192190 | TCATGAGAGAGCTTT[A/G]CCATTCCACAAGTAT | 55120 |
| rs370702600 | snp | G/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162335 | CATCCATAAACAGAC[G/T]ATGTAGAAAAGCCAA | 55120 |
| rs370706621 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227766 | GTCCTCACCTAGGTC[A/G]GTGGGCACAGGCCCG | 55120 |
| rs370733383 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58181368 | GCTTTGGTGGAAAAC[A/C]ATCAAAATAATGGGG | 55120 |
| rs370745619 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207805 | GACTCATGCCTATAA[A/T]CCCAGCACTCTGGGA | 55120 |
| rs370780049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58227285 | TCCATAGGCAGCTTG[C/T]GTTAGTCAGCTCAAT | 55120 |
| rs370792501 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58235610 | GCATTCATTATGTCT[A/C]GCATCCAATCAAGAT | 55120 |
| rs370894372 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58180575 | GGTGGGGGACTAGGT[A/G]AGGGATAGTATTAGG | 55120 |
| rs370906866 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186684 | TTACAGGTGTAGATA[C/T]GTATGTATGCCTTGT | 55120 |
| rs371054266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211057 | ACAGCTACACTAGGC[A/G]GTGCCTCAGTAGGGA | 55120 |
| rs371059417 | snp | A/G | 1.65592e-05 | 0.00287738 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162976 | GAAAAAAATTATGCT[A/G]TGAACTTTGTAAAAT | 55120 |
| rs371115914 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58175628 | TAGGTATTGATGGGA[C/T]GTATCTCAAAATAAT | 55120 |
| rs371154063 | snp | A/G | 1.64838e-05 | 0.00287083 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204209 | ATGGTACTGAAGCAG[A/G]TATCCGCATACACAA | 55120 |
| rs371165395 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167108 | TCCCAGCTATTTGGG[A/G]GACAGAGGCAGGAGA | 55120 |
| rs371185001 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171121 | AACTGATCACAAAAT[C/T]TGAAGTAAAACACTC | 55120 |
| rs371191174 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58183876 | ACCCAGTTTGCAAGG[A/C]AATCACAGCTCTCAT | 55120 |
| rs371196539 | snp | A/G/T | 6.80467e-05 | 0.00583261 | intron-variant | FANCL | GRCh38.p7 | 2:58198676 | TACTATTAAAAAAGC[A/G/T]TAACATTAGACCATT | 55120 |
| rs371207959 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205833 | TGGGAATTTTTAAGT[A/G]CATGATAAAAGGGGG | 55120 |
| rs371215234 | snp | C/G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242830 | TTCTTATAAGGGACT[C/G/T]AAACAGGAATCTAGC | 55120 |
| rs371216600 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208772 | GCGTGTCTTTACTTC[A/G]TCTCTGTACACCAAT | 55120 |
| rs371223229 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217145 | TTTTTATATATAGAT[A/T]TATATATATATTTAT | 55120 |
| rs371255402 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200480 | AAATGGAAAATTTAG[C/T]TCATTTTGAGTTGCT | 55120 |
| rs371409919 | snp | C/G/T | 3.30329e-05 | 0.00406393 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159542 | CTTCCACAGTCAGCA[C/G/T]GGGGATCACAGACTT | 55120 |
| rs371433803 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58238448 | AAAAGATAACCAACA[C/T]AGAGAGCATCATTAC | 55120 |
| rs371450929 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198906 | TTGTGGTGGGCGCCT[A/G]TAGTCCCAGCTACTT | 55120 |
| rs371485095 | snp | A/G | 4.95675e-05 | 0.00497808 | intron-variant | FANCL | GRCh38.p7 | 2:58204109 | TTTCTGATCACAATA[A/G]CAGTTTAACGAGGCA | 55120 |
| rs371504051 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202422 | TCTCAAAGACAGCTA[C/T]GGTGTATATATGAAA | 55120 |
| rs371522975 | snp | C/T | 3.86526e-05 | 0.004396 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161659 | AAAGAAAAATATTTA[C/T]AAAAAGCGTATGTGT | 55120 |
| rs371524685 | snp | A/G | 6.64441e-05 | 0.00576347 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160209 | AGATAAAGGAGAAGC[A/G]TCAGCATGATTACAA | 55120 |
| rs371556562 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238390 | ACAGTGAGACAATAA[C/T]TGTTTTTGTTTTAAG | 55120 |
| rs371587235 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181584 | GAAAGTATTCAGATA[C/T]CTGCAAGTTACTTTG | 55120 |
| rs371587757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58166146 | CTTGATATACTACAC[A/G]TATGCAATAGTAATG | 55120 |
| rs371626362 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221783 | AATTTTTTATGATGA[C/T]ATCCCTCTCTTTAAT | 55120 |
| rs371655652 | snp | C/T | 0.00043667 | 0.0147697 | intron-variant | FANCL | GRCh38.p7 | 2:58198553 | ACTGTACTTTTTAAT[C/T]ACTTAAAACAAATTT | 55120 |
| rs371659651 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58176248 | CCCATCAAGCTACCA[A/G]TGACTTTCTTCACAG | 55120 |
| rs371683819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182770 | TTCAATACAGCAACT[C/G]TGAATAATGTGTCTA | 55120 |
| rs371698749 | snp | C/T | 8.94782e-05 | 0.00668813 | intron-variant | FANCL | GRCh38.p7 | 2:58222079 | GAATTAGCTGTGGAA[C/T]GCAAGACAATGAACT | 55120 |
| rs371718569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212137 | AAGAAAGAGGTTTAA[C/T]TGGACTTACAGTTCC | 55120 |
| rs371824942 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216428 | TAGCCAAGGGCAAAT[A/G]CAGCAGGGGCAATGA | 55120 |
| rs371862623 | snp | A/C | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164296 | ATACACTGTAGAATA[A/C]GCCTTTCACTAAGGC | 55120 |
| rs371921135 | snp | C/G | 1.85458e-05 | 0.00304509 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241343 | AGAAACACAGAAAAG[C/G]TCTAGACCTGCTGGG | 55120 |
| rs372037880 | snp | A/C | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159269 | TAACATTTTATTTAG[A/C]ATTCTTACACACTAC | 55120 |
| rs372048411 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58176717 | TTCAGGACATAGGCA[C/T]GGGCAAGGACTTCAT | 55120 |
| rs372097604 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200061 | AACACAAAGGCAAAT[A/G]GATAAGAAATCATAT | 55120 |
| rs372101290 | in-del | -/A | 0.00524111 | 0.0509579 | intron-variant | FANCL | GRCh38.p7 | 2:58226708 | TGGTAACAGTGTCAG[-/A]AAAAAAAAAAAATTC | 55120 |
| rs372127636 | in-del | -/TG | | | intron-variant | FANCL | GRCh38.p7 | 2:58227664 | CAACGTCCAGCCACT[-/TG]TGTGTGTGTGTGCCT | 55120 |
| rs372155101 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211629 | TTATTTTATGCTGTT[G/T]CCCTTTTAAAACTAA | 55120 |
| rs372161649 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58188101 | TAATTTTTGTATATG[C/G]ATCGATGAGGTCATT | 55120 |
| rs372240390 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58189225 | TCAAAACTCAGCAAA[C/G]TGTACACCTTAAATA | 55120 |
| rs372267680 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58240200 | AGCTAGGTAATTCAA[A/G]AAGAATACTTCTAAT | 55120 |
| rs372282838 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220479 | AAGTAGAAGGCAAAG[A/G]CAACGAAAATAATTC | 55120 |
| rs372412141 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170109 | CAAGGTTGAAATGAA[A/G]GAAAAAATGTTAAGG | 55120 |
| rs372477534 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58166583 | GAGTTTCTCATGAAA[A/C]AATGTGGTATGTTTA | 55120 |
| rs372608600 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184044 | CAAGAATTCTAAATA[G/T]AACTGTTTGAAAATC | 55120 |
| rs372682280 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237038 | AACACCCCCTCTCAC[C/T]AACTGATAGAAAAAG | 55120 |
| rs372719547 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159731 | GATAATTTTTTAAGT[G/T]TCCAGCTCTTCACCG | 55120 |
| rs372722648 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58237674 | ATCTAGATGTATCGG[A/G]GGAAAAAATGAGACA | 55120 |
| rs372754560 | snp | C/T | 0.000280327 | 0.0118357 | intron-variant | FANCL | GRCh38.p7 | 2:58165677 | TTTATTTTCATAATA[C/T]AAAATAAAACACCTA | 55120 |
| rs372767610 | snp | C/T | 1.94801e-05 | 0.00312084 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241350 | CAGAAAAGCTCTAGA[C/T]CTGCTGGGTCCTGCA | 55120 |
| rs372784934 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178415 | AACCCTAGGATTCAA[C/G]GCTGGTTCAACATAA | 55120 |
| rs372785408 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164586 | AGCAAATCATGCCTG[G/T]AGGAGAAAAAAGAAG | 55120 |
| rs372811058 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195944 | TCTCATACATGTGCA[C/T]AAGGAAACATGGAAG | 55120 |
| rs372814889 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58225713 | CAGATTACAAAGAAA[C/G]TAGAATATGTTAAAA | 55120 |
| rs372896363 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166651 | ATCAAAACAGTTTAA[A/T]AAGAAGGATTTGTTT | 55120 |
| rs372900953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181092 | ATCCATAAAAATACC[A/G]TTACCGGAATGCTCA | 55120 |
| rs372906353 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241590 | AGCCTCAATTGTCCC[A/G]GGAGCCCTTTCGATG | 55120 |
| rs372907056 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58210426 | GAAACCGCCCTCCCA[A/C]AACACATGAGAACTG | 55120 |
| rs372911833 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232481 | AGAAATTCCTTCAAA[A/C/T]TGCTTTAATGGAAGA | 55120 |
| rs372929511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58213603 | CTAGGCCAGGCATGG[C/T]AGCGAACACCTGTTA | 55120 |
| rs372961987 | snp | C/G/T | 0.000101899 | 0.00713726 | intron-variant | FANCL | GRCh38.p7 | 2:58241185 | ACGCTGCAAGAGGCT[C/G/T]TCTTAGCTAGAAAGC | 55120 |
| rs373033673 | snp | A/T | 0.000153988 | 0.00877327 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159806 | AGGTAATTGGCTTTA[A/T]AAAGAGAACATATTT | 55120 |
| rs373042513 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198387 | AAATGCATTGTATTA[C/G]GTATTATAATCTAGA | 55120 |
| rs373105042 | in-del | -/CTGT | 0.0142736 | 0.0832652 | intron-variant | FANCL | GRCh38.p7 | 2:58191684 | TATAGATAATAATTG[-/CTGT]CTGACAGATATGTGT | 55120 |
| rs373161108 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58218130 | TTTTAACTGATAGTA[A/G]TAGAAATATAACATC | 55120 |
| rs373175790 | in-del | -/GTT | | | intron-variant | FANCL | GRCh38.p7 | 2:58193262 | TTTAAATGAAACTTT[-/GTT]AAGTGACAAGCATAG | 55120 |
| rs373237140 | snp | C/G/T | 0.00016443 | 0.00906605 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163116 | TAATTGCATGCTCTA[C/G/T]TCTTGGTTTCTAAAG | 55120 |
| rs373252087 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58166987 | GGGAGGCTGAGGTGC[A/G]CAGATCACGAGGTCA | 55120 |
| rs373253571 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217157 | GATTTATATATATAT[A/T]TATATATTTTATATA | 55120 |
| rs373270652 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198857 | TACGGTGAAACCTCG[C/T]CTCTACTAAAAAATA | 55120 |
| rs373364584 | snp | A/C | 1.66029e-05 | 0.00288117 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162875 | ACTTACAGATTTTTC[A/C]AGGATAGCACGAGCT | 55120 |
| rs373377667 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58209417 | ATTTGCAGTTATTCA[A/G]TGACATGGATTTATG | 55120 |
| rs373384384 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58186602 | AAGAACCAGAATGCA[A/T]GAGCATTTTTTTCCG | 55120 |
| rs373405000 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | FANCL | GRCh38.p7 | 2:58174026 | AAACCAACAAAGATC[A/G]AAAGAGACAAAGAAG | 55120 |
| rs373491616 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208653 | AAGACAGACTGAAGA[C/T]CTTCATGTTTGAATA | 55120 |
| rs373493158 | snp | A/G | 6.60404e-05 | 0.00574594 | intron-variant | FANCL | GRCh38.p7 | 2:58204119 | CAATAACAGTTTAAC[A/G]AGGCACATACCTTTG | 55120 |
| rs373506534 | snp | C/G | 1.67281e-05 | 0.00289202 | intron-variant | FANCL | GRCh38.p7 | 2:58229806 | TAAACCTTTTAAAAA[C/G]GACTTACCTGTTGTA | 55120 |
| rs373638792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166746 | AATAATTTAAGAATA[C/T]GATACACCCTAAGAT | 55120 |
| rs373653865 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215936 | TCATAATACAAGGAG[A/G]AATTAATTGGAATTC | 55120 |
| rs373761140 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199324 | CAAATGAGTTGATAT[A/T]TAATTTTCTTCTAGT | 55120 |
| rs373854636 | snp | G/T | 4.97022e-05 | 0.00498484 | intron-variant, downstream-variant-500B, synonymous-codon, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160090 | CATTTTATGAGATGT[G/T]ATTAACAATTTGCTT | 55120 |
| rs373863775 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187007 | TGGAAGACAGTGTGG[C/T]GATTCCTCAAGAATC | 55120 |
| rs374010008 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174136 | ACCCAGATTCATAAA[A/G]CAAGTCCTGAGTGAC | 55120 |
| rs374025218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58190400 | GAAAGCTCCTCAAGC[A/C]CATGCTGAAAATAAG | 55120 |
| rs374060779 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219175 | AAAAAAAAAAAAATA[G/T]ATATATATATATATA | 55120 |
| rs374081102 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207917 | TTTTAAAACTAACTC[A/C/G]TCATGGTGGCGTGCA | 55120 |
| rs374093014 | snp | A/G | 0.00013844 | 0.0083187 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161667 | ATATTTATAAAAAGC[A/G]TATGTGTCTCACTAA | 55120 |
| rs374100498 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210998 | TGTGCAAGCTGTCAG[C/T]GGATCTACCATTCTG | 55120 |
| rs374143605 | snp | C/T | 1.66136e-05 | 0.00288211 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160211 | ATAAAGGAGAAGCGT[C/T]AGCATGATTACAAAT | 55120 |
| rs374165109 | snp | A/T | 5.77684e-05 | 0.00537409 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161660 | AAGAAAAATATTTAT[A/T]AAAAGCGTATGTGTC | 55120 |
| rs374192999 | snp | A/C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171892 | CCCGGAAAATCGGGT[A/C/G]ACTCCCACCCCAATA | 55120 |
| rs374195602 | snp | A/G | 0.00011532 | 0.00759255 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165794 | CCAGGTCTTCTCATC[A/G]ATTTCATCCATAACA | 55120 |
| rs374236117 | in-del | -/A | 0.0022113 | 0.0331777 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163084 | TTACCACTTCAGATT[-/A]AAAAAAAAAAATTTA | 55120 |
| rs374301486 | in-del | -/AT | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58165112 | AAAGGCTGAAGTCAC[-/AT]GTTTTGCTTGCTTAT | 55120 |
| rs374302037 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221992 | GCTTGAGTAGAACTG[C/G]GGAGGAGGAGGTAGT | 55120 |
| rs374366064 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192299 | AACTATAGCGATATA[A/G]TATCTTCTTTAATCT | 55120 |
| rs374389238 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174687 | CACAAGAGAAAGCAG[C/G]AAAGATCCAAAATTG | 55120 |
| rs374414809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204320 | TGAAAATATTTGCTA[C/T]ATTCCTATTAATCCA | 55120 |
| rs374415004 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169127 | TGCCTCCTCAAGCAG[C/G]GGTCAAAAGACAACT | 55120 |
| rs374422445 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58232326 | AAAACTTTGTAGTTA[C/T]TGGGAAATCAAAACA | 55120 |
| rs374424645 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230233 | AATGTATCAAACATG[A/T]ATTTGAAAAAGCATG | 55120 |
| rs374428065 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213517 | TCTTCTGCTAAAACA[C/T]TCTTTATTTTTAAAC | 55120 |
| rs374437241 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191315 | CAACATTAAAGGAGT[C/T]ATTTGGAGACTGATA | 55120 |
| rs374448630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214563 | ACCTAGACTGAAGTG[A/C]AGTGGTGTGATCTCA | 55120 |
| rs374452719 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192891 | AAAAACCTTGCAAAC[C/T]TAACTTCTGAAGCTA | 55120 |
| rs374507719 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58228892 | ACCATTTTTTCCCAT[C/G]CTATTTCAATATGTC | 55120 |
| rs374521238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179137 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 55120 |
| rs374539676 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181773 | ATTTGTAATAAAACA[C/T]TGGAGGGGGGAATGA | 55120 |
| rs374547278 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | FANCL | GRCh38.p7 | 2:58171944 | AAAAAACGGCACACC[A/T]GGAGATTACATCCCG | 55120 |
| rs374549169 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172938 | AATACAGAGAAGTGC[A/T]TAAAGCAGCTGATGG | 55120 |
| rs374568736 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187676 | ATTCCCTAAGAGCTA[A/G]GTAAATATATTTTGA | 55120 |
| rs374572843 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58218469 | AGCATCACTATAGAT[A/C]CTAAAATCATTTTTT | 55120 |
| rs374576833 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196660 | TAGAGAGTCACAAAC[C/T]GATTTTGTTAAATAA | 55120 |
| rs374580291 | snp | A/G | 1.66394e-05 | 0.00288434 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232059 | ACCATATCACCTTGC[A/G]TTCTTCAGTTGTAAA | 55120 |
| rs374599100 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58178770 | TAAAAGGTATTCAAA[C/T]AGGAGGAGAGGAAGT | 55120 |
| rs374655920 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FANCL | GRCh38.p7 | 2:58221099 | GCGCCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG | 55120 |
| rs374672012 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204182 | CCAGAAGCATCTTCT[A/G]CTTTTAACTTGATGG | 55120 |
| rs374675609 | snp | C/G | 9.94201e-05 | 0.00704983 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226755 | CAACTCCATCATAAA[C/G]CTCATTAGATCAGGA | 55120 |
| rs374683786 | snp | A/G | 6.90667e-05 | 0.0058761 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159355 | TTTCCATAGGAAAGC[A/G]CAAGGAGAAGACAGA | 55120 |
| rs374687261 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172800 | GAGAATGACTTTGAC[A/G]AGTTGAGAGAAGAAG | 55120 |
| rs374699085 | snp | A/G/T | 8.25899e-05 | 0.00642565 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159543 | TTCCACAGTCAGCAC[A/G/T]GGGATCACAGACTTA | 55120 |
| rs374748612 | snp | C/T | | | | | GRCh38.p7 | 2:58243557 | CATTCACCTTTACTA[C/T]TGATACACTGGACAG | 55120 |
| rs374750427 | snp | C/T | 1.70206e-05 | 0.00291719 | intron-variant | FANCL | GRCh38.p7 | 2:58198677 | ACTATTAAAAAAGCA[C/T]AACATTAGACCATTT | 55120 |
| rs374836948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188790 | AAAAAAAAAGAGCTG[C/T]TGGGATTTTGATTGC | 55120 |
| rs374928731 | snp | A/C | 9.04527e-05 | 0.00672445 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163407 | TTATGACTCTATTAA[A/C]AAACGTTTAAATCTC | 55120 |
| rs374960980 | snp | A/C | 0.00050698 | 0.0159133 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241347 | ACACAGAAAAGCTCT[A/C]GACCTGCTGGGTCCT | 55120 |
| rs374960998 | snp | C/T | 0.00058183 | 0.0170463 | intron-variant | FANCL | GRCh38.p7 | 2:58232002 | ATACCAAATGTACTG[C/T]CTGTCCCACCAAAAT | 55120 |
| rs374985852 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191612 | AGAAAACTCCTTGTT[C/T]ACTGCACGTAAATAA | 55120 |
| rs375024937 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194768 | TGCAAGTTATAATTA[C/T]TCATCCAAATGAATA | 55120 |
| rs375041681 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239926 | TTTAGACACGTAAAA[C/T]GTTTAAGATTTAAAT | 55120 |
| rs375074601 | snp | A/C | 1.70038e-05 | 0.00291575 | intron-variant | FANCL | GRCh38.p7 | 2:58232134 | AAAATATTGAAAAGG[A/C]TCACTCAAATTTTTA | 55120 |
| rs375075791 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201426 | ATCACACACAGTATT[C/T]TTTAGACTCTATAAT | 55120 |
| rs375109863 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163708 | TTGATATGATTATCA[C/T]TGAAAGGATCTTAAA | 55120 |
| rs375113632 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189655 | GAATGTAACGCTTAT[C/T]ATCTTTAAAAGCATT | 55120 |
| rs375197324 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241441 | ATCCTGGAGGATTCC[A/G]CGGGCGGAAATGAAG | 55120 |
| rs375317278 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204055 | TAACTAGCACTTCTT[C/T]ACATTGAGAGCATTC | 55120 |
| rs375325401 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170629 | AGGAGATCCATCTCA[C/T]GTGCAAAGAAACACA | 55120 |
| rs375332065 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183575 | ACTCTGCTTCATTGA[C/T]TTTATTCTAATCTTT | 55120 |
| rs375414034 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58203826 | GTGTCCACTGTCTTC[C/T]ACATGTTACATGTAG | 55120 |
| rs375419273 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58175699 | AATGGGCAAAAACTT[C/G]AAGCATTCCCTTTGA | 55120 |
| rs375422145 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214552 | GTCTCACTGTCACCT[A/G]GACTGAAGTGCAGTG | 55120 |
| rs375471309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165304 | GGTCTACTGCAAGTT[A/C]TTTTATCTTCCTCTG | 55120 |
| rs375483641 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204468 | GTGTCAAGGCTCATG[-/G]CTGTGGTCAGTGAGC | 55120 |
| rs375504895 | snp | C/T | 1.65688e-05 | 0.00287821 | splice-acceptor-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160180 | TAGTCCTCTCAGCCA[C/T]TGCAAATTTTAAAAG | 55120 |
| rs375504998 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58199046 | AAAAAAAAAAAAAAA[-/G]AAAAACGAGATATAT | 55120 |
| rs375526911 | snp | C/T | 0.000232234 | 0.0107733 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162885 | TTTTCCAGGATAGCA[C/T]GAGCTGGAAAATCAA | 55120 |
| rs375626670 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | FANCL | GRCh38.p7 | 2:58204237 | CAAGTCTGGTGAGCA[A/G]AGGAGAATAAAAAAT | 55120 |
| rs375672771 | snp | A/G | 3.76783e-05 | 0.00434024 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161652 | TCCTTCAAAAGAAAA[A/G]TATTTATAAAAAGCG | 55120 |
| rs375705760 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58225091 | GCAAACAAGCTTGGG[A/T]TATATTAAATAAAGA | 55120 |
| rs375878155 | snp | A/C/G | 3.94791e-05 | 0.00444278 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241358 | CTCTAGACCTGCTGG[A/C/G]TCCTGCACATGCGCA | 55120 |
| rs375898409 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227286 | CCATAGGCAGCTTGT[A/G]TTAGTCAGCTCAATT | 55120 |
| rs375939352 | in-del | -/AG | | | intron-variant | FANCL | GRCh38.p7 | 2:58209579 | TACTATAAAACTCAG[-/AG]GCAGTCTGACAGTCA | 55120 |
| rs376006932 | snp | A/G | 5.0166e-05 | 0.00500804 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159746 | TTCCAGCTCTTCACC[A/G]AAATGTTGTATTCTT | 55120 |
| rs376041448 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58212407 | CAACTCAAGATGAGA[C/T]TTGGGTGGGGACACA | 55120 |
| rs376043580 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58211920 | AGCAACTAGTCTCTA[G/T]GAAGTTCCAAACTCT | 55120 |
| rs376071214 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163537 | AATGAAACAAGATTA[A/C]ATCTTTTAGAAGTAG | 55120 |
| rs376129811 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58216454 | AATGAGAAAAGGTAC[A/T]CTAACTAGTATGCCT | 55120 |
| rs376180961 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211032 | TCTGGAAGATGGTGG[C/T]CCTCTTCTCACAGCT | 55120 |
| rs376207402 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232424 | ACCAGGCCCATAGAA[A/G]AAATTTCAGTGTTAT | 55120 |
| rs376210968 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214308 | TTAGAACAATGGGTA[C/T]AATACAAAGCAAAAG | 55120 |
| rs376224867 | snp | C/G/T | 0.000150671 | 0.00867847 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241294 | CACTGGCGCAACAGG[C/G/T]TCGCTTCCGTCACCG | 55120 |
| rs376229390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237877 | CTAAGAGATTAAAGA[C/G]AATGTGCATCTTTAT | 55120 |
| rs376235726 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218437 | GGCACAAAAAACTCA[C/T]GTGGAAAGAAAAAGG | 55120 |
| rs376250296 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178452 | CAATAAACGTAACCC[A/G]TCACACAAACAGAAC | 55120 |
| rs376302617 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162325 | GTATTTGAGCCATCC[A/G]TAAACAGACTATGTA | 55120 |
| rs376384949 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58231155 | AGTTCCTCTTTAGTG[A/T]CCAGTCCTTTAAATG | 55120 |
| rs376390237 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161826 | ACAATTCTTCTAACT[A/G]CTTTAGAATACGAAA | 55120 |
| rs376396127 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58192108 | AAGTAAATCAGTTAA[C/T]GTACCAATGAAGGCA | 55120 |
| rs376515275 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58226196 | ATCTTCCCTCTTCTT[C/T]TGTTTATGTTGAAAA | 55120 |
| rs376516013 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238138 | ACAAATTAATAAACT[C/T]TCTTAAAACATTATG | 55120 |
| rs376528147 | snp | A/G | 6.63372e-05 | 0.00575884 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162886 | TTTCCAGGATAGCAC[A/G]AGCTGGAAAATCAAT | 55120 |
| rs376550296 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58187741 | CTTTAATGGTAGTAA[-/AA]GTGTTATCCTTGAAA | 55120 |
| rs376617166 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205589 | ACTTCCAGAAAAATT[A/G]ATCATTTAAAAAATG | 55120 |
| rs376624896 | in-del | -/TTTCCAAT | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242112 | TTCCAATTTTCCAAT[-/TTTCCAAT]GCATCACGTTTGAGC | 55120 |
| rs376687535 | in-del | -/AAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58164714 | TGGGGCCACGAAAAT[-/AAT]GATTTACTACATTTC | 55120 |
| rs376716140 | snp | C/G | 4.95225e-05 | 0.00497582 | intron-variant | FANCL | GRCh38.p7 | 2:58204121 | ATAACAGTTTAACGA[C/G]GCACATACCTTTGCC | 55120 |
| rs376742771 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58221644 | CTCAGCATTACTCTT[A/C]AAACATGGAAAATTT | 55120 |
| rs376818265 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203588 | AAAATTTGTGATTAT[A/T]GATCACTATCCTATA | 55120 |
| rs376831871 | in-del | -/CTCT | | | intron-variant | FANCL | GRCh38.p7 | 2:58191922 | ACAGATATTCTTTCT[-/CTCT]TTTTATAAATAAGTA | 55120 |
| rs376851945 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | FANCL | GRCh38.p7 | 2:58229776 | TTTAGTAATTTCTTA[C/T]CTTCACTGAAAACAT | 55120 |
| rs376879842 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226540 | CAAAGAGGTTCCTTC[C/G]AACAGTTATGTCCCT | 55120 |
| rs376885541 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58234516 | AAGTGGAACACAGAC[A/C]CAAAAAAGTCCAGAG | 55120 |
| rs376930947 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58195580 | AGGATGTGACCAGAC[G/T]GAAAGTTAAACTCTG | 55120 |
| rs376956540 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197645 | CTAATATCATCAATG[C/T]ACTGCGAAATTCAAC | 55120 |
| rs376979561 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237448 | CCAAAATGTGTGTGA[C/T]ATAGCTAAACCAGTA | 55120 |
| rs376991511 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222888 | CTACAATAAATAACG[A/G]AAGTAGATAGGGACA | 55120 |
| rs377027863 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229779 | AGTAATTTCTTATCT[G/T]CACTGAAAACATAAA | 55120 |
| rs377033981 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213283 | GGCGGGGCCTTAAAC[A/G]GTAGCAATTCTAGTA | 55120 |
| rs377039440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240318 | ACATATACTCAAAGA[C/T]TATGCGTGATGGTGG | 55120 |
| rs377052216 | snp | A/G | 4.97253e-05 | 0.004986 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160185 | CTCTCAGCCACTGCA[A/G]ATTTTAAAAGATAAA | 55120 |
| rs377060600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58174495 | AAACTCACTCAAAAC[C/T]GCTCATCTACATGGA | 55120 |
| rs377118172 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213610 | AGGCATGGCAGCGAA[C/T]ACCTGTTAATCCCAG | 55120 |
| rs377127125 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58176807 | AACTAAAGAGCTTCT[A/G]CACAGCAAAAGAAAC | 55120 |
| rs377144813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236150 | GCTCCACAGACCTTA[C/T]GGAGGAAAAACATGA | 55120 |
| rs377232955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210634 | ATCTAAGACAAGGCA[A/G]GTCTCTTCCACCGAT | 55120 |
| rs377236769 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204167 | ATTAAATGCTCTCTA[A/C]CAGAAGCATCTTCTG | 55120 |
| rs377297886 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203358 | ACAATTGATCTTTTC[A/G]TCACTACAATCTTCT | 55120 |
| rs377398832 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213716 | TTGTCTCTTAAAAAA[-/G]AAAAAAAAAAAAAAA | 55120 |
| rs377401239 | snp | C/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243125 | TTAAGAGAACATATA[C/G]TCCCTTACTTCAAGC | 55120 |
| rs377408383 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58230401 | CTGAACTCCTAGGCT[A/C/T]AAGAAACCCTCCCGC | 55120 |
| rs377429618 | snp | A/C | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204200 | TTTAACTTGATGGTA[A/C]TGAAGCAGGTATCCG | 55120 |
| rs377436957 | snp | C/T | 8.31069e-05 | 0.00644566 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159394 | GAGTCTCAAGAACCT[C/T]TGAATGAAGTAAACA | 55120 |
| rs377534926 | in-del | -/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242640 | ACCTTTGACAACTTA[-/C]CCCAGTTTATTACCA | 55120 |
| rs377535042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206693 | AGGTAATACACTACA[A/G]AAAAAGTGCCACGCT | 55120 |
| rs377541119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58218837 | ACATATGGTAATGGA[C/T]TGGAGTTGTAGACAT | 55120 |
| rs377555984 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218709 | TCTGATAGTGCTCTG[C/T]ACGTATACTGCAACT | 55120 |
| rs377648081 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229824 | CTTACCTGTTGTACT[A/G]TTCGATGGTATCCAC | 55120 |
| rs377703252 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186054 | AAAATTTTTCAAATA[C/G]TGACAAGTCAAAGGA | 55120 |
| rs377723951 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217175 | TATATTTTATATATA[G/T]ATATATATATATATA | 55120 |
| rs377725250 | snp | C/T | 5.73784e-05 | 0.00535592 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161657 | CAAAAGAAAAATATT[C/T]ATAAAAAGCGTATGT | 55120 |
| rs386646475 | in-del | C/GT | | | intron-variant | FANCL | GRCh38.p7 | 2:58171590 | TGAACCCAGGAGCTG[C/GT]TTTTTGAAAAGAGTA | 55120 |
| rs386646476 | in-del | ATATCCTTTAATTACATA/TGAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58194006 | GCTATGTAATAGGAC[ATATCCTTTAATTACATA/TGAC]TCCTTTAATTACAAA | 55120 |
| rs386646477 | in-del | C/GA | | | intron-variant | FANCL | GRCh38.p7 | 2:58202696 | CCTTGAAAAAGTATA[C/GA]AAAAAGCAGACAAAA | 55120 |
| rs397752216 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58215718 | CAAAAAAAAAAAAAA[-/A]GCATCATTTCCGCCA | 55120 |
| rs397753969 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228079 | ATGGTCATTTTTTTT[-/T]ATTTTTCCCTTGACC | 55120 |
| rs397779532 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223015 | TATATCAATTTTTTT[-/T]AACCAGGATAGGACA | 55120 |
| rs397871498 | in-del | -/A/AT/T | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58222326 | GAGATAAAAAAAAAA[-/A/AT/T]TTTTTATTAAATTCA | 55120 |
| rs397977975 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58177802 | AGATTAAAAAAAAAA[-/A]GAAAAAGAAAAAACA | 55120 |
| rs527244587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161436 | ACTATTGACTCAACA[C/G]ATTTTAGATTCTGTG | 55120 |
| rs527282716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167139 | ATCACTTGAACCCGG[A/G]AGGCAGAGGTTGCAG | 55120 |
| rs527294638 | snp | A/G | 1.67492e-05 | 0.00289384 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198658 | TCTGGTGATTCTGCA[A/G]GATACTATTAAAAAA | 55120 |
| rs527323173 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58238245 | TTCCAATGTGACCCA[A/G]GGAAGCCAAAAGATT | 55120 |
| rs527413624 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205281 | GTAATGAAAATATGT[C/G]TAAATCTGAAGATAT | 55120 |
| rs527439353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218125 | AATATTTTTAACTGA[C/T]AGTAATAGAAATATA | 55120 |
| rs527443580 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58211284 | CTGCCAAGGCTTGGG[A/G]TTTGCACCCTCTGCA | 55120 |
| rs527467999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58180124 | TTGACACTGTTGGTC[A/G]AAGTGTAAATTAGTT | 55120 |
| rs527503398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175444 | ATCCACCATGATCAA[C/G]TGGGCTTCATCCCTG | 55120 |
| rs527535029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179661 | AGGCAAAACCATTCA[A/G]TACATTGGCATGGGC | 55120 |
| rs527552719 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222599 | TGCCATCCATCTGGC[C/T]AGATTACAGTCCCGT | 55120 |
| rs527554721 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58185938 | ACATATTAGTACCTA[C/T]CACTGAAATATTGAG | 55120 |
| rs527603905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224720 | ATAGACAGGAAAAGC[A/G]TAAGTGAAATATAAC | 55120 |
| rs527658440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184737 | TAGAAATCAAGTTAA[C/T]GCAGAAGCCTCTCAG | 55120 |
| rs527665563 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58191023 | ATCTTTATTCTCCAA[C/T]GGGCATGTTTTTCAG | 55120 |
| rs527685510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162413 | TCTGTCATTAATGAC[A/G]TCACTACTGAAGACC | 55120 |
| rs527686579 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183687 | TTTCCATATTTTCTA[C/T]AACATTTTTATAATC | 55120 |
| rs527695254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185142 | GAATCTAATCTTCCT[A/G]TGGTGAAAAATCAAA | 55120 |
| rs527723357 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180174 | TGTGGCGATTCCTCA[A/G]GGATCTAGAAGCAGA | 55120 |
| rs527765808 | in-del | -/TG | | | intron-variant | FANCL | GRCh38.p7 | 2:58190163 | TGTCTGGTCAAACAC[-/TG]TTATCTGTCAAGCAA | 55120 |
| rs527792387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237310 | TAAATTATAAATCAA[A/T]AACAAAAAGATATCT | 55120 |
| rs527794915 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211454 | GAGTGGCTGCCGTGA[A/T]GACCTCTGGCATGCC | 55120 |
| rs527828992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58197113 | CTCTCTTCTCTATTT[C/T]GCTATGTTTTCTCAA | 55120 |
| rs527854941 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58203886 | TGAGTCTATAAAATT[C/G]TAACTGTAGTATTTG | 55120 |
| rs527865062 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231511 | GTCACAAAATCCTCT[C/G]AATTCTACTCATAAA | 55120 |
| rs527886890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196506 | ACAAAACAAAACTTG[A/T]ATGACCCAATTAAAC | 55120 |
| rs527902245 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230175 | TTTTCCAAGATAGGT[C/T]AAATAAAACCAACAG | 55120 |
| rs527940840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170515 | TCATAATGACAGGAT[A/C]AAATTTACACATAAA | 55120 |
| rs527949191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58174627 | CAGAATCTCTGGGAC[A/G]CATTCAAAGCAGTGT | 55120 |
| rs527981064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216268 | ACCCACTTGGGCCCT[C/T]TGCCAATCTGTTCCC | 55120 |
| rs528024404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58210609 | TCAAAAGTCCACAGT[C/T]CAAAGTCTCATCTAA | 55120 |
| rs528173427 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58221807 | CTTTAATTCACAGCA[A/C]CAATAAGGATCAAAT | 55120 |
| rs528178133 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229187 | CAGGAAAAAAACACA[C/G]AAATGCATAAAGCAT | 55120 |
| rs528193890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58222311 | ACTATTATGCCTATC[A/G]GAGATAAAAAAAAAA | 55120 |
| rs528241141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183821 | GAAATTAACATTTTA[C/G]CCATGTACAGGACTA | 55120 |
| rs528266241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188463 | GTTTTTTTTTGAGAT[A/G]GGGTCTCTCTGTCAC | 55120 |
| rs528270425 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58222207 | TCATGAAAAAGAGAC[A/C]AGAAAAAGTTAAAGG | 55120 |
| rs528304810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58183218 | AATAGAAAAAAATGA[A/G]TAAAGACATAATTCC | 55120 |
| rs528313074 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219627 | ATAACATGTACCCTT[C/G]ATATGAAGAGAAGAA | 55120 |
| rs528318449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235784 | AAGGAAAACATGAGC[A/G]TACTAAATAGAGACA | 55120 |
| rs528372331 | in-del | -/AAATATATATA | | | intron-variant | FANCL | GRCh38.p7 | 2:58219170 | AAAAAAAAAAAAAAA[-/AAATATATATA]TATATATATATATAT | 55120 |
| rs528408578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195207 | GAAGTCTCACATTTC[C/T]TCTTATTTTCAAAAC | 55120 |
| rs528437688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209078 | CAACATTCATCTCCT[C/T]TAAGAACTCTCCTAA | 55120 |
| rs528443928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214807 | TGTGAGCCACCACAC[A/C]TGGCCCATGAGGAAT | 55120 |
| rs528455623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58201831 | AGATCGTGAGGGGAA[A/G]TGGTAGAATTGGGAA | 55120 |
| rs528460616 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163918 | ACATTTCATAGAACT[A/G]TGGCCAAATGTAAAA | 55120 |
| rs528464214 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240216 | AAGAATACTTCTAAT[A/T]GGAGAGGGAAAGGTG | 55120 |
| rs528480242 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238105 | GGCAGCCCAGGACAG[C/T]TCTGAATGCAGCCCA | 55120 |
| rs528491121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194634 | TGATTTCTTACTACT[C/G]TAAATGTCTCCTCTG | 55120 |
| rs528520363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240853 | CTCATCAACATCCGT[A/G]GAGGTGGAGGGTGTT | 55120 |
| rs528539809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173286 | AAAGAAATACAGAGA[A/C]TGCCACAAAGATACT | 55120 |
| rs528602600 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216626 | TGAAAATAAAGAAAA[A/G]TAGAGAAAAACCCTT | 55120 |
| rs528636870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221014 | TCAGGAGATCGAGAC[C/G]GATCCTGGCTAACAC | 55120 |
| rs528641328 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169562 | ATGAGTTTGACAAAC[G/T]GACAGAAGTAGGCTT | 55120 |
| rs528644664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182472 | TTCATCATAACTTTG[A/G]CTTTCGTTGTTAATG | 55120 |
| rs528672825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177208 | CTAGTTCAACCCTTG[C/T]GGAAGTCAGTGTGGC | 55120 |
| rs528765102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227416 | AGTGCAAGGTTTTAT[C/T]AAGTGCAAGTAGCTC | 55120 |
| rs528803572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58220522 | TAATCACAGTGCATT[C/T]TTATCACCTCTAGAA | 55120 |
| rs528807457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181832 | AATTACGTATGAGTT[A/C]TTTGTTATAACTGAG | 55120 |
| rs528839772 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58202046 | TAACATACAGTTAAC[A/G]TTTCAACTATTAGTG | 55120 |
| rs528864727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187271 | TCCTTTGTTGGGACA[C/T]GGATGAAGCTGGAAA | 55120 |
| rs528945207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233610 | CCTCAAATTACCTAC[A/T]GGAAGAAAAATATGA | 55120 |
| rs528977744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199283 | TGAACCAAACTGGAT[A/C]TCTGTTTATCTTTAA | 55120 |
| rs528996529 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204381 | AACCCTTTCTGCTGC[C/T]ATAGATTTACTGCCG | 55120 |
| rs529010021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232827 | ATAACTTAAATAGGA[A/T]AATACACAGGAAACT | 55120 |
| rs529010099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239871 | TTGTACTGTATATCC[C/T]TGCTACTTTTCTGTA | 55120 |
| rs529013677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162582 | ATCTCTGTATACAGA[A/G]GGCCGACTTCTTCTA | 55120 |
| rs529037549 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58198814 | GCGGGCGGATCACAA[C/G]GTCAGGAGATCGAGA | 55120 |
| rs529050391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172596 | TTAGCTGAGGGTCTG[C/T]GTGTTAACAGAAAAG | 55120 |
| rs529058523 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180904 | CTAATATTAATGAGA[C/T]AACATTAAAATAATA | 55120 |
| rs529201454 | in-del | -/T | | | frameshift-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161609 | TCAAGTTGATAAGCA[-/T]TAACAAATTCCACAA | 55120 |
| rs529222705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212541 | TGTCCTAGGCAAAAT[A/G]GTATGCATGATAAGC | 55120 |
| rs529222793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206206 | AGAGGTTTAAGAAAC[A/G]GTAAAGCTAATGGAA | 55120 |
| rs529253197 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176614 | CCCTTCCTTACACCT[C/T]ATACAAAAATTAATT | 55120 |
| rs529274749 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58174684 | GCCCACAAGAGAAAG[C/T]AGCAAAGATCCAAAA | 55120 |
| rs529281504 | in-del | -/A/AA | 0.541267 | 0.102209 | intron-variant | FANCL | GRCh38.p7 | 2:58194926 | TGTCTATTATATCAC[-/A/AA]AAAAAAAAAAGAAAA | 55120 |
| rs529308052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176018 | AAATCATGAGTGAAC[A/T]CCCATTCACAATTGC | 55120 |
| rs529313268 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237943 | TAGCTGCCATGTGTG[A/G]TAACAGTCAAGCAAC | 55120 |
| rs529330955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218882 | GTTTACCTTAATACA[C/G]ATATAAATGGTTATA | 55120 |
| rs529352787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224805 | ATTTTCAGAGTAAAA[C/G]TGATACAAGCAAACA | 55120 |
| rs529392868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225906 | TTAAGAGACTTATCA[A/C]CTAAATATAATGTGA | 55120 |
| rs529473525 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58177847 | AGACCGCTAGCCAGA[C/T]TAATAAAGAAGAAAA | 55120 |
| rs529480548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191724 | ATCCACAAATATACA[A/G]TATCATTACACATGG | 55120 |
| rs529509417 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171584 | AATCAATGAACCCAG[A/G]AGCTGGTTTTTTGAA | 55120 |
| rs529518507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192293 | AACTGAAACTATAGC[C/G]ATATAATATCTTCTT | 55120 |
| rs529552762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238162 | CATTATGGGATTTTT[C/T]GTGATTTTTTTTTAG | 55120 |
| rs529563604 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 2:58243673 | ATTGCTAATTTATCA[C/T]CTTAGATTTTAAAGA | 55120 |
| rs529586751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205223 | CTATATAATGATAAC[A/C]TGGGCTAATTTCAAG | 55120 |
| rs529590085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160543 | AATCCATTAATCACA[A/T]ATTAACAACTCCTGC | 55120 |
| rs529616392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204652 | CTCCTCAATGAACTT[A/C]TCCTATATTATCAAT | 55120 |
| rs529645756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191261 | CACTAATATTGAAAA[A/C]AATAATTTTTATCCA | 55120 |
| rs529707345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171417 | GAAATGCCCACATGA[C/G]AAAGCAGAAAGAACT | 55120 |
| rs529717404 | snp | A/G | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188587 | GGGGACTACAGACAC[A/G]TTGCCCCCACACCCA | 55120 |
| rs529720648 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58210847 | CTCCATGTCTCACAT[A/C]CAGATCATGCTGATA | 55120 |
| rs529722422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217415 | TTCTGGTGGCTGCCA[C/G]CAAGAAAAATATTTT | 55120 |
| rs529736821 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58192256 | TACAAAGCTTAAACC[A/C]ATTTTTATAATCTTA | 55120 |
| rs529755382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211250 | TCTGTGCACCCACAG[A/G]CTCAACAACATGTGG | 55120 |
| rs529770761 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58175119 | TAGACCAATAACAGG[A/C]TCTGAAATTGTGGCG | 55120 |
| rs529774469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171026 | CTGGACCAAGCAGAC[C/G]TAATAGACATCTACA | 55120 |
| rs529832410 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58179308 | AGAACAAAGCTGGAA[C/G]CATCATGCTACCTGA | 55120 |
| rs529883225 | in-del | -/ATTTTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58238198 | AGCTATCATTAGTGT[-/ATTTTA]ATTTTATGTGTGCCC | 55120 |
| rs529913041 | snp | C/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58230043 | TGTCTTCAAACTGTT[C/G]GTACTAATTTTATTT | 55120 |
| rs529915166 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193487 | ACTAAGTCTATAGGT[C/G]AAATGACTGCTACGC | 55120 |
| rs529920079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179561 | AACGGGACCCCTCCC[A/T]TACACCTTATACAAA | 55120 |
| rs529933214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174739 | AAGAACTAGAAAAGC[A/G]AGAGCAAACACATTC | 55120 |
| rs529940701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224159 | ATTACATGGCCAAGA[C/G]AGCTGTGACTTACAA | 55120 |
| rs529949344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58223472 | AAACCTGGATAATAG[C/T]AAAAACACTTTTCAA | 55120 |
| rs529991060 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240872 | GTGGAGGGTGTTAAA[A/T]TCGAGTTAAGGCAAA | 55120 |
| rs529993251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184643 | CAGAAATTAGCAACA[A/G]AAAACAACCCTTAAA | 55120 |
| rs530107619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165250 | TACTTAAAACTATAA[A/G]TTCTTTCTCTGTGCT | 55120 |
| rs530108140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236117 | TTAAATGAAAATATA[C/T]ACTCAGAGATCCAAG | 55120 |
| rs530118227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184014 | ACTTCTAAGGTGACT[G/T]CCAGGTATAGAAGTC | 55120 |
| rs530133754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203371 | TCATCACTACAATCT[G/T]CTGAAAAAGAGTTGA | 55120 |
| rs530136438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229397 | TATCTCCCCTCATTA[C/T]GCAAGTACACATGAT | 55120 |
| rs530162727 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232773 | ATTTATTCCATTTTA[C/G]TTTCTTGGAAAAGTG | 55120 |
| rs530188437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209927 | ATCAAAAACCTACCA[A/T]TATATGTTGACAATC | 55120 |
| rs530227335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58170101 | AGATTCATCAAGGTT[A/G]AAATGAAGGAAAAAA | 55120 |
| rs530227346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174074 | AAGGGATCAATTCAA[C/T]AAGAGGAGCTAACTA | 55120 |
| rs530245377 | in-del | -/TTAG | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58233394 | TCCAAAATTAGCTTT[-/TTAG]TTAAAGTATCTAGAA | 55120 |
| rs530248391 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58234789 | ACAGACTTCTTAAAG[A/C]AAATTAAAAAATGAA | 55120 |
| rs530287872 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58173769 | TCATAATGACAGGAT[C/G]AAACTCACACATAAC | 55120 |
| rs530376347 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222364 | GGCTTCACTATGGCT[C/G]TATTCCCATGAATAT | 55120 |
| rs530396061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214822 | CTGGCCCATGAGGAA[C/T]CTTAAGTCTTGCCTT | 55120 |
| rs530433434 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58215450 | AATGGAATAGCTTGC[A/T]AAAGACCAACACTTC | 55120 |
| rs530444458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178273 | AAAATCTGGAGGAGG[C/T]ACAACAGAAAAAGAA | 55120 |
| rs530445234 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58177793 | AAAATAAAAAAGATT[-/A]AAAAAAAAAGAAAAA | 55120 |
| rs530460549 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185623 | CTGGAAGTTATGAAT[A/G]AGTCAAAGACCCCGA | 55120 |
| rs530486437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235356 | CCATGTTCCAACCAG[C/G]CAGAGTGGAAACCTT | 55120 |
| rs530506933 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226446 | ATGTTAAACTCTCTG[C/T]TGATAGGCCAGGAGT | 55120 |
| rs530564570 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221679 | TACAGTTGTATGTTC[A/T]GTGAAAGTATCTATT | 55120 |
| rs530565786 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58222663 | TGTTTATGTTCTCCC[A/C]ACCAAAACTAAAATT | 55120 |
| rs530609254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58240689 | AGCAAAGTTAATTAA[C/T]TCCATTGCTGTCATG | 55120 |
| rs530685003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169489 | TCCAAAAACCAGAAC[A/G]CCTTTTCTCCAACGG | 55120 |
| rs530703357 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58199338 | TTTAATTTTCTTCTA[A/G]TCCTAAATTTAATTT | 55120 |
| rs530710619 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163717 | TTATCATTGAAAGGA[A/T]CTTAAATTTCAGCCA | 55120 |
| rs530736477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187795 | AAAACAACGTCCATT[C/T]TGAGTTTTATTATTG | 55120 |
| rs530741686 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224996 | TTTCCCACAAAGAAA[A/T]CATGATTCTTTGGAG | 55120 |
| rs530819895 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216906 | ATCCTTCATGATTCC[C/T]GACCCCCCAATCCTT | 55120 |
| rs530821506 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179548 | TGCAGAAAACTCAAA[C/G/T]GGGACCCCTCCCTTA | 55120 |
| rs530866619 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163338 | GACAAAAAATAAAAA[C/T]TACCATTAATATACT | 55120 |
| rs530888966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220402 | AACAAAAGGGAAAAA[A/G]TTGATCTACACATAA | 55120 |
| rs530889288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212779 | CCAGACCTGTCATAC[C/T]ATCTTCACGTTAACC | 55120 |
| rs530914097 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219351 | CATGAGTCCATAGTA[C/T]TTCAAATAAATGACT | 55120 |
| rs530921575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173025 | TGCGATCAACTGGAA[A/G]AAAGGGTATCAGTGA | 55120 |
| rs530925558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213512 | ACTTCTCTTCTGCTA[A/C]AACATTCTTTATTTT | 55120 |
| rs530981067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177184 | TTACACTGTTGGTGG[A/G]ACTGTAAACTAGTTC | 55120 |
| rs530981177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172758 | AAGGAACACAGCTCC[C/T]CACCAGCAATGGAAC | 55120 |
| rs531015058 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172227 | TTAAATGTCCCTGTC[C/T]GACAGCTTTGAAGAG | 55120 |
| rs531027272 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58222225 | AAAAAGTTAAAGGAC[-/T]GCACTGAAGGTCATG | 55120 |
| rs531148932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176616 | CTTCCTTACACCTTA[C/T]ACAAAAATTAATTCA | 55120 |
| rs531177206 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198100 | GTGGGTGTGTTTGTG[A/T]GTGCATGTAGAGAGG | 55120 |
| rs531179794 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181041 | ATATTCCTACCTTAA[C/G]CTGGCAATTCTACTC | 55120 |
| rs531180053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192511 | CAAAGGAAAATTAAT[C/T]ACCGTTAACCACATT | 55120 |
| rs531198278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232613 | TATACAGACATAAGT[A/G]AAATACTTGCATAAA | 55120 |
| rs531215903 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231303 | ATCTGCACTCCAGGT[C/T]TCACACTCTATTTCC | 55120 |
| rs531217593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193128 | ATAAATGTTTTTCTA[G/T]ATTTTGGCCATATTA | 55120 |
| rs531238642 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58232261 | TACTTGTTAAAATAT[A/C]TGCAACACAATATTG | 55120 |
| rs531322738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238758 | AAACCAAAAAGGACC[C/T]TCCACGAGAAAATTT | 55120 |
| rs531338351 | in-del | -/TTAATTTGTTTTATATTAATACCAC | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158759 | TGCATAAGTAACCAG[-/TTAATTTGTTTTATATTAATACCAC]TTAATTTGCTTTATA | 55120 |
| rs531338429 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182511 | AATATTCTATTTTAT[G/T]CCTGCGATAAATTTT | 55120 |
| rs531342337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58198758 | TTAGGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 55120 |
| rs531360490 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164177 | GTACTGGACTACAGC[A/C/G]TAAGTTTCAGAAATT | 55120 |
| rs531360519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239185 | ATGTGTGTGAAAGTT[C/T]GATGCCTCAGAGTAC | 55120 |
| rs531365056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205473 | GAATGTCTTTATCAC[A/G]TTTTACCATATGACT | 55120 |
| rs531396114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175833 | AATTAGGAAAAGAGG[A/G]AGTCAAATTGTCCCT | 55120 |
| rs531399514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171915 | CCCCAATACTGCGCT[A/T]TTCCGACGGGTTTAA | 55120 |
| rs531430925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172188 | GCACAGACAAACAAA[A/C]AGACAGCAGTAACCT | 55120 |
| rs531434334 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58206081 | AAGAATTGACAAAAA[C/T]TGGGAAGTAGAAATG | 55120 |
| rs531456576 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58175484 | GCTGGTTCAATATAC[A/G]CAAATCAATAAATGT | 55120 |
| rs531485365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212196 | GTGGAAGGCAAAGAG[G/T]AGCAAGTCCCATCTT | 55120 |
| rs531522271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211746 | AGTTCATAGTTCCAC[A/T]TATCTCTAGGGCAGG | 55120 |
| rs531576013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179743 | TGGGATCTAATTAAA[A/C]TAAAGAGCTCCTTCA | 55120 |
| rs531649863 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211206 | CTTCTGAAATCTAGG[C/T]GGAGGTTCTGAAACC | 55120 |
| rs531656861 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL | GRCh38.p7 | 2:58188663 | CCAGATGGTCTCCAA[C/T]TGCTGGGCTCAATCA | 55120 |
| rs531675843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231021 | ACTTGCATCTAACCT[A/C]TCTCTTTGTAATCCT | 55120 |
| rs531747743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180180 | GATTCCTCAAGGATC[C/T]AGAAGCAGAAATACT | 55120 |
| rs531751049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160453 | TGATAAGAATTACGC[A/G]TTTTCTTTATCCCCA | 55120 |
| rs531752803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185201 | TCTTAAGGAAAAAAT[A/G]GACATCTCCACATCA | 55120 |
| rs531782154 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242959 | CAAGCTCTCCAGGTG[A/C]TTCTGATGCATGCTA | 55120 |
| rs531813832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58164783 | TTCACAAATATACCA[C/T]AATTTGGTTAATTGT | 55120 |
| rs531814852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191128 | TAGCCCCTGGATTAT[A/T]AAAAAAAAAATTCAA | 55120 |
| rs531816784 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240663 | ACTCCATATGAGAGG[C/T]CACTGGAATCAGCAA | 55120 |
| rs531843739 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58224445 | TAATTAGGATTTATG[A/T]ACTCATAAATCAAAA | 55120 |
| rs531877379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58165963 | ACTCAATTTAGAAAT[C/T]TTAAGCTGTTTCATT | 55120 |
| rs531997395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171340 | GTTATTGAGAACAAA[C/G]ACACAATGTACCAGA | 55120 |
| rs531999472 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179923 | AAAGGATATGAACAG[A/T]CATTTCTCAAAAGAA | 55120 |
| rs532035074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166427 | AAGGTACAAATGATG[A/T]TTTTCCACATTTAAC | 55120 |
| rs532040276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170981 | ACGAGACACAAAATT[A/C]ACAAGGATATTCAGG | 55120 |
| rs532054843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58223352 | AAGATTGTGCTCTAC[C/T]AGTTATTAAATAAAA | 55120 |
| rs532128253 | snp | A/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161980 | AAAGCTATTGTAGGG[A/T]GTTTCCTTTTCCACT | 55120 |
| rs532137055 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58174670 | TTATAGCACTAAATG[A/C]CCACAAGAGAAAGCA | 55120 |
| rs532155018 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58228881 | AGACTACATAAACCA[-/T]TTTTTCCCATGCTAT | 55120 |
| rs532200855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174242 | AACAAGACAGAAAGT[C/T]AACAAGGATACCCAG | 55120 |
| rs532209083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215771 | AAAATAACAGACTGG[A/G]AAGGCCAGAATCTGG | 55120 |
| rs532214602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222402 | GATATATACATTTTT[A/T]AAAAAGTACCTCTAA | 55120 |
| rs532256601 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223803 | ACTCCCACTATATGC[A/T]GTAATTACTAGGAAA | 55120 |
| rs532331805 | snp | A/G | | | | | GRCh38.p7 | 2:58243418 | GGATAGGTAATCCGC[A/G]GAAATTAATTATTTC | 55120 |
| rs532337686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203260 | AAGATATCAACTTTT[C/T]TGTGTCATCCAGTAC | 55120 |
| rs532352178 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58219492 | AGCTACATATAGTGA[-/G]CTTCCAAAGAGTAAA | 55120 |
| rs532359670 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58235082 | AGCATAATATTCTCC[A/C]TGATGTGAGAAGAAA | 55120 |
| rs532365681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178954 | CAGACAAACAGAGAG[A/T]CAAATTATGAGTGAA | 55120 |
| rs532375787 | snp | A/G | 1.67217e-05 | 0.00289147 | intron-variant | FANCL | GRCh38.p7 | 2:58229877 | ACTACATAATAATCT[A/G]AAATTTTAATGAGAC | 55120 |
| rs532430579 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241571 | GACTGACCAAGATCA[C/T]TCTAGCCTCAATTGT | 55120 |
| rs532464732 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58169984 | AAAAACACTCTTCAG[G/T]ATGTTATCCAGGACA | 55120 |
| rs532472266 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159049 | GTTTTGCCAAGAAAA[C/T]TCAGTTTTCATATTC | 55120 |
| rs532495670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58202636 | TTGCAAAACTGACCC[C/T]GGAAAATATTCTCCA | 55120 |
| rs532499057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209164 | ATGTAAGTTTTAGCT[A/T]GCCAAACACATAATA | 55120 |
| rs532531782 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241297 | TGGCGCAACAGGCTC[C/G]CTTCCGTCACCGCCA | 55120 |
| rs532540197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188600 | ACGTTGCCCCCACAC[C/G]CAGCTGATTTTTGTA | 55120 |
| rs532560438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214718 | GGTTTCACCATGTTG[A/C]CCAGGTTGGTCTCAA | 55120 |
| rs532568618 | snp | A/C | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188604 | TGCCCCCACACCCAG[A/C]TGATTTTTGTATTTT | 55120 |
| rs532569550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235427 | GCTTCACTTGTAGAG[A/G]CTAACTACCTTAGAC | 55120 |
| rs532588938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164996 | CAGAATTTCAAAATA[A/C]CCTTGAACAACATAT | 55120 |
| rs532593339 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58190620 | TCTAATTTTTCATCA[A/C]TCTAAAATCAATGAA | 55120 |
| rs532621047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173693 | AATCATGCCAAATTG[G/T]AAAGACCATCGAGGC | 55120 |
| rs532651769 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58235948 | AGAGAAAGACATTGA[-/G]GGGAAAAAAAAATGA | 55120 |
| rs532653324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164503 | AATGGCTCCAGACAG[C/T]ACTTTCACGTAATAT | 55120 |
| rs532688258 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212496 | TATTTGAGACTGACA[C/G]GGGCCAAAACAAAAA | 55120 |
| rs532701290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208516 | TAGAAGAAATGTGTT[C/T]TACATAGCTCATAAA | 55120 |
| rs532768430 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169561 | AATGAGTTTGACAAA[A/C]TGACAGAAGTAGGCT | 55120 |
| rs532771583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58187652 | AGACAAGCAACTGAC[A/G]TAAGTTCAATTCCCT | 55120 |
| rs532774875 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218804 | TTCAGATATACCAAG[C/T]AAGTGGGCTACAAAA | 55120 |
| rs532839758 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58221052 | CCCCGTCTCTACTAA[A/G]AATACAAAAAATTAG | 55120 |
| rs532863732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214242 | TTCATATCCTTATTT[C/T]TGGCTTTCATCTATT | 55120 |
| rs532878896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221601 | TTATTCCAGAAATAC[C/T]GCAATTTTTCCAGTC | 55120 |
| rs532889385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166979 | AGCACTCTGGGAGGC[C/T]GAGGTGCGCAGATCA | 55120 |
| rs532932547 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58199926 | ACTACAGTATTTAAC[A/C]AACATTTGAAATCAA | 55120 |
| rs533006527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227847 | GCCGCCCTTCTGTAT[C/T]ACTACTATGTCTAGC | 55120 |
| rs533042341 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58172962 | CTGATGGAGCTGAAA[A/G]CCAAGACTTGAGAAC | 55120 |
| rs533076757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169058 | CTGCCTGCTGGCTCT[A/G]AAAAGAGCAGCAGAT | 55120 |
| rs533086374 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187288 | GATGAAGCTGGAAAC[A/T]ATCATTCTCAGCAAA | 55120 |
| rs533110817 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180797 | AGCTACTGTGCCATT[G/T]TTTAAAGGTTTTTTG | 55120 |
| rs533124361 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179759 | TAAAGAGCTCCTTCA[C/T]AGCAAAAGAAACTAT | 55120 |
| rs533153629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194000 | CTCCCTGCTATGTAA[C/T]AGGACTGACTCCTTT | 55120 |
| rs533182789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240024 | AATCTCAATTCTAAT[G/T]GGTGTACTTGTTTCC | 55120 |
| rs533188740 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58181068 | ACTCCAAAAAAAGTG[-/AA]AAGATATATCCATAA | 55120 |
| rs533254729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219068 | ACCAGGACTCCTTGG[A/G]AAAATGGCTGATTCT | 55120 |
| rs533299734 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58207716 | AGATCTTAAAGGAAA[A/C]AAAGAGTGATAAACT | 55120 |
| rs533319398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212679 | GCCATTCTGTAAAAC[A/T]ACATGGGCAGAAGTT | 55120 |
| rs533331720 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196841 | AGTATAATTTAGAAA[C/T]AACACCTGGAAAGAG | 55120 |
| rs533377225 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58221157 | GGCGGAGCTTGCAAT[A/C]AGCCTAGGCAACAGA | 55120 |
| rs533378114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58186767 | AAGAAGTAAAGTGGC[A/G]GAACCGCAGTGAATT | 55120 |
| rs533379841 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58207033 | AAGTTTTAGCAGGAT[A/C]CACTTCACCCAGCTA | 55120 |
| rs533395494 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58226011 | ATTTAAAAACAGATA[A/C]AAAGCACTTAGCTGT | 55120 |
| rs533395803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232602 | GTTACACAATCTATA[A/C]AGACATAAGTGAAAT | 55120 |
| rs533550702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186351 | ATATCTTCATCTGTA[C/G]CATACAACAATGACA | 55120 |
| rs533605220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58236861 | ACATTATTACTAAAG[A/G]TAAAAAAGGTCATTT | 55120 |
| rs533632493 | in-del | -/A | 0.00159712 | 0.0282137 | intron-variant | FANCL | GRCh38.p7 | 2:58218315 | GCAGATATTAATGAT[-/A]AAAAAAATATACAAC | 55120 |
| rs533632672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204731 | TGATCCTCTAAGGAA[A/C]ATGCTGTATAAGCAC | 55120 |
| rs533640901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196830 | ATAAATATTAAAGTA[C/T]AATTTAGAAATAACA | 55120 |
| rs533658622 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212378 | TCCTGCAACACATGG[C/G]AATTGTGGGAGTACA | 55120 |
| rs533725021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192382 | CATTTACTTAAGAAA[C/T]ACCATTGGTATTTTA | 55120 |
| rs533763210 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242649 | AACTTACCCCAGTTT[A/G]TTACCATTAGACCAT | 55120 |
| rs533787581 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235415 | TCAGAAGGTGTTGCT[A/T]CACTTGTAGAGACTA | 55120 |
| rs533787725 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58210899 | CTTGGGGAGCTAGAC[A/C]CCTGTGATTTTGCAG | 55120 |
| rs533796780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58170706 | AAGCAAAAAAAAAAA[A/G]AAGCATGGTTTGCAA | 55120 |
| rs533858872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210896 | GACCTTGGGGAGCTA[C/G]ACCCCTGTGATTTTG | 55120 |
| rs533873729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160730 | CCTTAGAGTATTTCT[A/G]TAATTTGACCTGTAT | 55120 |
| rs533908333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58179050 | GGACCTCTTGAAGGA[G/T]AACTACAAACCACTG | 55120 |
| rs533911686 | snp | C/T | 0.000248742 | 0.0111494 | intron-variant, downstream-variant-500B, missense, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160075 | ACTGAAAGCTAGGCA[C/T]ATTTTATGAGATGTG | 55120 |
| rs533978456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171066 | ACCCCAAATTAACAA[A/C]ACATACATTCCTCTC | 55120 |
| rs533987128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216068 | GCTTTGTCAAAAATG[A/G]ACCCCAAACTGTAAT | 55120 |
| rs534016104 | in-del | -/A | 0.475877 | 0.107142 | intron-variant | FANCL | GRCh38.p7 | 2:58240111 | TAACATGCTTCCTGT[-/A]AAAAAAAAAAAAAAA | 55120 |
| rs534070331 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184150 | CATTTATTACCAATT[A/C/T]TTGTTTATAAAGAGA | 55120 |
| rs534100638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58188771 | CTTAAATTAGGAAGG[A/G]AAAAAAAAAAAAGAG | 55120 |
| rs534130437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58183484 | TCAGTGAAGAGGTCA[A/G]CATTTTGTAGGTCCT | 55120 |
| rs534174131 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58226277 | AGGATAAACTGAATA[A/C]TCAAGTATTTTATGC | 55120 |
| rs534248413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223549 | GGTAAGTTACTCCTA[C/T]TGTAGAACCGTAACA | 55120 |
| rs534259402 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178503 | TTATCTCAATAGATG[C/T]AGAAAAGGCCTTCAA | 55120 |
| rs534259483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229517 | CTGATTTTTTTTCCC[C/T]ATCACCACCATTCAG | 55120 |
| rs534262204 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181330 | ATGCCTCTGTTTATA[A/G]TATCTGGAATAGACA | 55120 |
| rs534307565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169730 | TGATGAAGCTGAAAA[A/G]CACAGCACGAGAACT | 55120 |
| rs534340302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170158 | TGGGTTACCCACAAA[A/G]GGAAGCCCATCAGAC | 55120 |
| rs534340612 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164284 | TTGATAAATTCCATA[C/T]ACTGTAGAATAAGCC | 55120 |
| rs534368159 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58196188 | TGCACGGATGGCCTA[C/T]ATACCAATTTTGGGT | 55120 |
| rs534372937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173478 | GAGAGTGGGAGCCAA[C/T]ATTCAACATTCTTAA | 55120 |
| rs534380793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180179 | CGATTCCTCAAGGAT[C/G]TAGAAGCAGAAATAC | 55120 |
| rs534400347 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241796 | TAACACATTGATTAT[A/G]TCATATATATTACAG | 55120 |
| rs534404920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214431 | CTCTACCCTTCTTAT[C/T]GTGGTCATAATTCAG | 55120 |
| rs534409602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189362 | ACTAACAGCTTCTCG[A/T]TAGTTTTCTCAACAA | 55120 |
| rs534486660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202892 | TATTTAAAATCTTTA[C/G]TTTTGGTCTTCATAG | 55120 |
| rs534497528 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171468 | ACAATTAAAAGAACT[A/G]CAGAAGCAAGAACAA | 55120 |
| rs534505962 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203406 | TTGACTCCAAGAATA[A/G]TTAAAAAAAAAAAGT | 55120 |
| rs534533413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177878 | GAGAGAAGAATCAAA[C/T]AGACACAATAAAAAA | 55120 |
| rs534550549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202105 | TCTTTTTTTTTCCCT[A/G]AAATTTTTGTTTCCT | 55120 |
| rs534557201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209404 | TTACTACTAGATAAT[C/T]TGCAGTTATTCAATG | 55120 |
| rs534593434 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58215888 | GGATAAAAAGTCAAG[A/C]AGAAAGGCAATGAAA | 55120 |
| rs534596847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173862 | GGATAAAGAGTCAAG[A/G]CCCATCAGTGTGCTG | 55120 |
| rs534615419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58227965 | GAGGTATAGGAGTGA[C/T]GTGAGTGGGAAGAGG | 55120 |
| rs534634111 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58241087 | CCTTTAGTCTCCCAA[C/G]AGCCGTTACGCGCCG | 55120 |
| rs534669509 | snp | A/C | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162281 | GAGAAACTATAACTG[A/C]TTCACAAACACTTAC | 55120 |
| rs534678439 | snp | A/G | 0.000136827 | 0.00827011 | intron-variant, missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58194242 | ACAGGCAAAACCGCA[A/G]TTTTCACATCCATTT | 55120 |
| rs534686761 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186696 | ATATGTATGTATGCC[C/T]TGTGGCTTCCACAAG | 55120 |
| rs534702343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240260 | CCATATGGAATAATG[A/T]ATTTTTAACCTCTAC | 55120 |
| rs534711273 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212959 | TTATTTTAAATATTT[C/G]TTTTTCTTTTCCAAC | 55120 |
| rs534729695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233940 | GAAACTTAGGCTCTT[A/C]TACGAGTAAATAAAA | 55120 |
| rs534736742 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58214844 | TCTTGCCTTATGTAT[A/C]CTTAGTGCTTTACAT | 55120 |
| rs534788006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58207868 | TCAAGACCAGCCTGG[A/G]CGACACAGTGAGACC | 55120 |
| rs534789040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182753 | ATGATGTCCTAATAC[A/G]ATTCAATACAGCAAC | 55120 |
| rs534829701 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192098 | TAACATCAGCAAGTA[A/G]ATCAGTTAACGTACC | 55120 |
| rs534842698 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58227936 | AGGAGGAAGAGAAAA[A/C/G]AAAAGAGAAAGAAGA | 55120 |
| rs534925147 | in-del | -/AAAG | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58196988 | TTTTTTAAAATAAAA[-/AAAG]AAAGCTATAAAATTT | 55120 |
| rs534928789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220877 | GGCAATCTAAATGGA[A/G]ATAATAAATGAATAC | 55120 |
| rs534958426 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172570 | GGTCTGTTTGTTAAC[A/G]GAAAGGACTCTTAGC | 55120 |
| rs534970072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212452 | AAACCATATCATAAA[A/G]TGATATGTATTTCTT | 55120 |
| rs534983938 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58187116 | AAAACACATGCACAC[A/G/T]TATGTTTATTGCGGC | 55120 |
| rs534987151 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58224212 | AGAAGAGTTTAATGG[A/G]ACATGATATCTATAC | 55120 |
| rs534991403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58219935 | TAAAATCCCTACTGC[A/G]TATCTTAGGACTATT | 55120 |
| rs535018953 | snp | A/G | 0.000203807 | 0.0100927 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163402 | GGATTTTATGACTCT[A/G]TTAAAAAACGTTTAA | 55120 |
| rs535032622 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183912 | TGGTAACAAGGTATT[G/T]GATCTTAAGCAAGAC | 55120 |
| rs535054761 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58176786 | TTGACAAATGGGATC[C/T]AATTAAACTAAAGAG | 55120 |
| rs535090766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181392 | AATGGGGATTTACTA[C/G]GATGGGACAAAACCC | 55120 |
| rs535100521 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200217 | GCTGTAATCACTGGA[A/G]AAACAATTTGTATGC | 55120 |
| rs535158133 | snp | A/C/T | 0.000430493 | 0.0146661 | synonymous-codon, missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162923 | AACATCTTTCAAATT[A/C/T]TGTAACACACTATTT | 55120 |
| rs535172334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192589 | ATATCTTCATAATAA[G/T]GTAAACACTGAATAT | 55120 |
| rs535205273 | in-del | -/AAAA | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58189388 | AACAATTAGGAACTT[-/AAAA]AACACAAAATAGTAA | 55120 |
| rs535273352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186125 | GCAAGGAAATAATTT[A/G]AGAGAAGCCTAGTGC | 55120 |
| rs535320412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58236642 | CATATGAATAACCAC[A/G]TTAAATGTAAATAGT | 55120 |
| rs535378461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197424 | CACTAGAAATGTTTT[C/T]TCTCTTTGCCTAAGA | 55120 |
| rs535402273 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208627 | TAACATCAACAGGCA[C/G]ACTGCTTCAAAAGAC | 55120 |
| rs535408123 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178152 | TCACAGCCAAATTCT[A/C]CCAGAGGTACAAAGA | 55120 |
| rs535442730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176268 | TTTCTTCACAGAATT[A/G]GAAAAATCTACTTTA | 55120 |
| rs535496148 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167296 | CGGTATAATGTCTGT[A/T]CTCTTCTGGTATACT | 55120 |
| rs535501650 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243341 | CCTGCTGCATCGTAG[A/G]TGCTAATAAATTATT | 55120 |
| rs535545115 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58226311 | ACTGATTAAACAGTA[C/T]ATATGTAACAGTATA | 55120 |
| rs535593963 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232298 | AGGGAAAATAACTCA[A/G]AACTGTCTTACAAAA | 55120 |
| rs535641432 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161603 | GGTACCGTCAAGTTG[A/G]TAAGCATAACAAATT | 55120 |
| rs535684283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238798 | ATTAAGGTGCATAGT[A/G]AATTGACATCATATA | 55120 |
| rs535704473 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198157 | AGGAAATATAAAAGA[A/G]GCATTATAGAAGGTG | 55120 |
| rs535733052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205588 | TACTTCCAGAAAAAT[C/T]AATCATTTAAAAAAT | 55120 |
| rs535743835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58230410 | TAGGCTCAAGAAACC[C/T]TCCCGCCTCAGCCTC | 55120 |
| rs535831175 | in-del | -/GC | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58198897 | GCCAGGCATTGTGGT[-/GC]GGGCGCCTGTAGTCC | 55120 |
| rs535843488 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242586 | AAATATCCTTATCTC[C/T]AAAGAAACGGAGACA | 55120 |
| rs535855955 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172902 | GAAAAAAATTTAGAC[A/G]AATGCATAACTAGAA | 55120 |
| rs535874314 | snp | C/T | 0.00011582 | 0.00760899 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159425 | GTTTCCCACAAAAAA[C/T]CAGCTATACACAATT | 55120 |
| rs535880971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58236631 | TTAAATCCAACCATA[C/T]GAATAACCACGTTAA | 55120 |
| rs535947903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203619 | AGGGATCTATAAATA[A/G]AGGCATAACCTCTGC | 55120 |
| rs535984291 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58196270 | AGGGACAGAAAAGGG[G/T]GTCAGGTCTTAGCTA | 55120 |
| rs535993193 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58183329 | AGTTACAGGATGGTG[-/A]AAAAAAAATTAAGTA | 55120 |
| rs535994628 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175258 | CAATCAATAGAAAAA[C/G]AGGGAATCCTCCCTA | 55120 |
| rs536058182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58179892 | AAGAAAAAAACAACC[A/G]TATCTAAAAGTAGGC | 55120 |
| rs536078291 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58167499 | GTTAACTCCCCTGCC[-/A]AAAAAAGAGTTATAA | 55120 |
| rs536146368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215915 | GAAAAACAAGATTTA[A/G]AAAGTTCATAATACA | 55120 |
| rs536154860 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58231046 | AATCCTCAGCATTGC[A/T]AACCATGCCTTGCTT | 55120 |
| rs536187180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184905 | AAGTACATTCTACTT[C/T]GCCTTCCACAAAAGG | 55120 |
| rs536202344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58196676 | GATTTTGTTAAATAA[C/T]AAAATAAAGTACTAA | 55120 |
| rs536211896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58189700 | ATACCTGAAGTGAAG[C/T]AATAATGTCAGTCAC | 55120 |
| rs536221497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183437 | TCTCTTACAGCACTC[C/T]CCTTATTAGTTACTG | 55120 |
| rs536242024 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58230454 | ACTACAGACACCCAC[A/C]ACCAAGCCTGGCTAG | 55120 |
| rs536324623 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58184951 | CGTGTTGAAGGCACA[C/T]CAACCCACCACAGAC | 55120 |
| rs536340533 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58188064 | ATTTATGTTTTTACA[C/T]TGTTTATAATTCATT | 55120 |
| rs536342551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195428 | CACATTCAAATTGTA[C/T]AAGCATATAGAATAT | 55120 |
| rs536357184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228517 | TTTGTAAACAAAGTT[A/T]TATTGGCATGTAGCC | 55120 |
| rs536407316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194903 | TTTAATATGGATGCC[A/T]CAAAGCCATGTCTAT | 55120 |
| rs536442482 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164240 | CTGCTTAAGATCAAT[G/T]TGGATTTCATTTTCA | 55120 |
| rs536514194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222677 | CAACCAAAACTAAAA[C/T]TTTTTACAAGACACA | 55120 |
| rs536580160 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58211793 | CTCTTTGCTAAAACA[-/T]TAACAAGAGTAACCT | 55120 |
| rs536631235 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203387 | CTGAAAAAGAGTTGA[C/T]TGATTGACTCCAAGA | 55120 |
| rs536669223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173393 | GCCAGAGAGAAAGGT[C/T]GGGTTACCCACAAAG | 55120 |
| rs536671661 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228521 | TAAACAAAGTTTTAT[C/T]GGCATGTAGCCATAC | 55120 |
| rs536722013 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58228013 | TCAGGCAACTCTATG[A/T]AATTTTTAAAATCTA | 55120 |
| rs536790135 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58177354 | TATTGCAGCACTATT[A/C]ACAACAGCAAAGACT | 55120 |
| rs536835374 | snp | A/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159837 | TAACAAAGTTTGTGG[A/T]CACTCTAAAAAATAA | 55120 |
| rs536836570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58241007 | CCGCTCCACGCCGCG[C/T]GCCTCCTCGCTCCCC | 55120 |
| rs536856377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176983 | AAGGACATGAACAGA[C/T]ACTTCTCAAAAGAAG | 55120 |
| rs536882188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235023 | TCTGGTTCTATGATG[C/G]GAGTATTTTCAGGCT | 55120 |
| rs536933792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58201022 | TAAAAAGAACATTTA[C/T]GTAAGTCTGGATGAT | 55120 |
| rs537011360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199762 | AAATACCCATTTCTT[C/T]TCATTAAAAAGCTAA | 55120 |
| rs537044759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239005 | TAAAAGTCCATGCAT[C/T]CATTCTAATATAATT | 55120 |
| rs537054891 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58189416 | TAGTAACAATCCTCA[A/C]AGTAAGGACAAAGAA | 55120 |
| rs537084200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214353 | TTAGCTCACAAAACA[A/C]TTACTCCATATTTTA | 55120 |
| rs537092533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207990 | CTTGAGCTGAAAAGT[C/T]TGAGGTTGCAGTGAG | 55120 |
| rs537097832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198844 | ATCATCCTGGCTATA[C/T]GGTGAAACCTCGCCT | 55120 |
| rs537148985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58213714 | CCTTGTCTCTTAAAA[A/G]AGAAAAAAAAAAAAA | 55120 |
| rs537170483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207119 | CCAGTGGACTACAAG[C/G]ACAAGTGATGTGTGC | 55120 |
| rs537213500 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58174933 | TCAAATAGATGCAGT[A/G]AAAAATGATAAAGGG | 55120 |
| rs537241484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227004 | AATTTGCTGAGATAT[A/T]TTAAACTGTGTTAGA | 55120 |
| rs537250768 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58172884 | GAAGAAGCTGAAAAC[-/T]TTGAAAAAAATTTAG | 55120 |
| rs537260631 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58181507 | ATGCACTTTACTGTT[A/T]CCAAATTTTACAAAG | 55120 |
| rs537272855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220125 | TATTACATGCAATCG[C/T]GATTTTAGTAAGGTT | 55120 |
| rs537290858 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235772 | TTCAAGAAGGTAAAG[A/G]AAAACATGAGCGTAC | 55120 |
| rs537314683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218464 | AAGGCAGCATCACTA[C/T]AGATCCTAAAATCAT | 55120 |
| rs537330030 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232632 | TACTTGCATAAATCA[C/G]AGTATATTTAATTCT | 55120 |
| rs537342285 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193729 | TCCAGTTGGTCAAAA[C/G/T]AACTTCCACAGGATT | 55120 |
| rs537359728 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227366 | CCTGCCTTGGTGTAC[G/T]GGAAAAATTGGATCA | 55120 |
| rs537388187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187079 | GGTATATACCCAAAG[A/G]ATTATAAACCATGTT | 55120 |
| rs537399488 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58192867 | AAGAAAACAAAAACA[A/T]CAACAACAAAAAACC | 55120 |
| rs537459406 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162306 | ACTTACATCAAGCTA[A/C]TCAGTATTTGAGCCA | 55120 |
| rs537479025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225205 | TTAAATATATAAAAA[C/T]CTATGAGTTCATAAA | 55120 |
| rs537497892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231163 | TTTAGTGACCAGTCC[C/T]TTAAATGTTGGTACG | 55120 |
| rs537500321 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224655 | GAAATATCAAAACTT[C/T]CCATTGTTAGCAATA | 55120 |
| rs537508736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167977 | TTTTTTCCCCAAATT[A/G]AAAAAAATAAATTAT | 55120 |
| rs537537070 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58206373 | TATTTCAAAGTATTT[C/G]TCTCAAAGAATAAGA | 55120 |
| rs537564042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198937 | GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 55120 |
| rs537579188 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185575 | CACTGAAGCACCATC[A/T]GTTGCTTTTGGCAAT | 55120 |
| rs537584283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191948 | AATAAGTAATTTACA[C/T]AAGGTCATGCACTGG | 55120 |
| rs537608852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197380 | AGCCAAAATGAGTAG[C/T]CTCCATTTACGGAAT | 55120 |
| rs537625064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176183 | TAGGAAGAATCAATA[C/T]CATGAAAATGGCCAC | 55120 |
| rs537706179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166138 | TTATAATGCTTGATA[C/T]ACTACACGTATGCAA | 55120 |
| rs537759648 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58215885 | AGAGGATAAAAAGTC[A/C]AGCAGAAAGGCAATG | 55120 |
| rs537787213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175697 | TGAATGGGCAAAAAC[C/T]TGAAGCATTCCCTTT | 55120 |
| rs537821255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186027 | CCACTGTTAGTTATA[A/C]AGTAGTCACAGAAAA | 55120 |
| rs537839887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231557 | TTTCCTCCATTCTTC[A/T]CCAGAAATATTTAGA | 55120 |
| rs537856003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180400 | AGCCATAAAAAAGGA[C/T]GAGTTCATGTCCTTT | 55120 |
| rs537864858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175188 | AGATGGATTCACAGC[C/T]GAATTCTACCAGAGG | 55120 |
| rs537892034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210933 | ATGGCACCCCCACCC[A/G]GCTGAGTTCATGGGC | 55120 |
| rs537897114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58238325 | AGATCATGAGAGATT[C/T]TGATCAAGAACTACC | 55120 |
| rs537972203 | snp | A/G | 3.32486e-05 | 0.00407715 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161495 | GTGTTAGCGGAAAAA[A/G]GTCTTGACAATATTT | 55120 |
| rs538008548 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160811 | TTCTCCATTGGCAAA[C/G]TACAGACGGCACCAA | 55120 |
| rs538016525 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243287 | AAGCTTTTTTAATCT[C/T]CTGAAAATTATTGCT | 55120 |
| rs538037883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166754 | AAGAATATGATACAC[A/C]CTAAGATGAAAAGAA | 55120 |
| rs538058121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179103 | CAAACAAATGGAAAA[A/G]CATTCCATATTCATG | 55120 |
| rs538106751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236247 | TAAAAGCAGCCAGAG[A/G]AAAAAAATATTCTAT | 55120 |
| rs538195743 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178626 | CCACAGTCAATATCA[C/T]ACTGAATGGGCAAAA | 55120 |
| rs538222604 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241410 | GCGGAGCGGAAACCC[C/T]AGCCTTGGCGGGAAG | 55120 |
| rs538239224 | in-del | -/TAAT | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58222849 | ATTACAAAAAGTAAA[-/TAAT]TAATTAATTAAATAA | 55120 |
| rs538247632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164760 | TTTTCATTCTTAGTA[C/T]CTACTTGTTCACAAA | 55120 |
| rs538283124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58217558 | GCTTGTGTAGTTATA[A/G]CAAAGTAGACATTAA | 55120 |
| rs538309023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170262 | AAAGAATTTTCAAAC[C/T]AGAATTTCCTATCCC | 55120 |
| rs538537404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196220 | AACAGTTACTACTTA[A/G]AGGGAGAGAAGCAAA | 55120 |
| rs538600302 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58195636 | AAGACATGCCACAGA[A/G]ATATTTATATCCCAT | 55120 |
| rs538628695 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236319 | AACAGTGCAAGACAG[G/T]GAAGTAACATCTTTA | 55120 |
| rs538648770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234975 | CAGTGATCCTTGAAA[G/T]AAGGGAAACAAATGT | 55120 |
| rs538658728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182822 | AGATACTGGTGATAC[G/T]AACAATATAGAAGAT | 55120 |
| rs538672540 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232896 | TCTTTTACTCTAACA[C/G]AATAAAATGAAAAAG | 55120 |
| rs538674058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228007 | TAAAAATCAGGCAAC[G/T]CTATGTAATTTTTAA | 55120 |
| rs538697764 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238703 | AACAATACTGTCTAA[C/T]TACAATACAAGAAAA | 55120 |
| rs538713797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240911 | AAAAAAAATTAAAAA[A/C]CAGTCAATTGCGGGA | 55120 |
| rs538735294 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58202003 | ACTTAAAACTTAGTT[G/T]GGATTAAGATTTTGC | 55120 |
| rs538739097 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186989 | GAACTAGTTCAACCA[C/T]TGTGGAAGACAGTGT | 55120 |
| rs538741030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210156 | AATAAATGTATCTTA[G/T]AAAGTGTATTAGTCT | 55120 |
| rs538797537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200923 | ATATCTGAGTTAAAT[A/G]AGTATTTGCAATATG | 55120 |
| rs538803072 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183384 | AAAGTAGCTTTTCCA[G/T]CATTAACTGAGATAG | 55120 |
| rs538815317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173523 | AACCCAGAATTTCAT[A/G]TCCAGCCAAACTAAG | 55120 |
| rs538817216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178478 | AGAACCAAAAACAAA[A/T]ACCACATGATTATCT | 55120 |
| rs538847085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169216 | AGAAAGGAACAGGCA[A/G]CAAAATCTTTGCTGT | 55120 |
| rs538855879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173938 | AATAAAAGGATGGAG[A/G]AAGATCTACCAAGCA | 55120 |
| rs538918430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173071 | ATGAAATGAAGCAAG[A/G]AGGGAAGCTTAGAGA | 55120 |
| rs538927908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58214447 | GTGGTCATAATTCAG[C/T]ATTACTATGATCAAC | 55120 |
| rs538933803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207451 | ACAATGCAGTCACAG[C/T]GGATGGCTGAGAAAC | 55120 |
| rs538962918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183314 | ATTGCAGAGCTTCAG[A/T]GTTACAGGATGGTGA | 55120 |
| rs538976354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178056 | AAGAAGTCAAATCCC[A/G]AAATAGATCGATAAC | 55120 |
| rs538988105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207911 | AAATCTTTTTAAAAC[G/T]AACTCGTCATGGTGG | 55120 |
| rs539021395 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181647 | GAAGAAAGGATGAAT[A/G]AATGGAAAAACATGA | 55120 |
| rs539027559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176869 | TGGGAGAACATTTTC[A/G]CAACCTACTCATCTG | 55120 |
| rs539044903 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58205814 | GATATACTGGCAGAA[A/T]TTATGGGAATTTTTA | 55120 |
| rs539062352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222917 | CAAGTTGAAAATTAT[A/G]AACACTTCTGAAAAA | 55120 |
| rs539064553 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58177322 | TGCTGCTATAAAGAC[A/G]CATGCACATCTATGT | 55120 |
| rs539079308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234168 | GACTCACAAGATTTC[A/G]GGTGATAACAGACTC | 55120 |
| rs539170453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164137 | CTAAGAAAATTGGCA[A/C]TAGGTTCTTTTATAC | 55120 |
| rs539207285 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164927 | CCAGATAATCTATAT[C/T]ATACCTAGGTATAAA | 55120 |
| rs539207286 | snp | A/C | 1.68875e-05 | 0.00290576 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163440 | ATGTCATACCATGGT[A/C]AGCTCCAAGAAAGAA | 55120 |
| rs539245901 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163150 | CATTTGATACAGAAT[A/G]TTTCTTAACTACTTG | 55120 |
| rs539253359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58180836 | TGCCCATTTGTAATG[C/T]GCAAAGTAATCAAAA | 55120 |
| rs539257943 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187051 | ACCATTTGACCCAGC[A/C]ATCCCATGACTGGGT | 55120 |
| rs539274481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168823 | CTCACAGTGTATACA[A/G]TGCCACGAGGAAGCT | 55120 |
| rs539278173 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58168830 | TGTATACAATGCCAC[A/G]AGGAAGCTGGAACTG | 55120 |
| rs539283537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232930 | TAAAATTCTCAAAAA[A/C]CAATTACCATGTGGA | 55120 |
| rs539421608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161709 | TACATATTTGGGAGG[A/G]TATGTGTGATATTTT | 55120 |
| rs539437945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167379 | CCCAAGAAGCTAGTT[G/T]TAAAATCAGTACAAT | 55120 |
| rs539457516 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58213223 | AAATCATTGTGTGTG[A/T]CATTTCAAAAGATAA | 55120 |
| rs539474930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167865 | CGAACTTAGGGGGTA[C/G]ACATCAAAACTATTA | 55120 |
| rs539529492 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227529 | CTGGTCGAACTCCAC[A/G]TCATTCTGCCGGTCA | 55120 |
| rs539558275 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175129 | ACAGGCTCTGAAATT[C/G]TGGCGAAAATCAATA | 55120 |
| rs539573131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212333 | TGGGGGAAACTGCCC[C/T]CGTGATTAAATTATC | 55120 |
| rs539582467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58186598 | GTCCAAGAACCAGAA[G/T]GCAAGAGCATTTTTT | 55120 |
| rs539622022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175304 | CCAGCATCATTCTGA[C/T]ACCAAAGCCGGGCAG | 55120 |
| rs539632371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232410 | TTACAAAATTGCTAA[A/C]CAGGCCCATAGAAGA | 55120 |
| rs539671199 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242595 | TATCTCTAAAGAAAC[A/G]GAGACATAGAAAAGA | 55120 |
| rs539672063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226396 | TTTATACATCATATT[A/G]TATCTTTAAGTAGGA | 55120 |
| rs539674506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58238923 | CATACATAAAACCTG[C/T]TCACTGGCCAAATCT | 55120 |
| rs539692922 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208466 | TTTTTGTTGTTGTCC[C/T]TGTTAATAGCTGAAT | 55120 |
| rs539697717 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220612 | TTCTTTAGTTATCAG[A/G]TAATGGTATAAAATA | 55120 |
| rs539716293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231460 | ATTTGAAAAGCATCC[G/T]CTATTCCTTTTTCCC | 55120 |
| rs539717987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58224538 | ACCTTAGAAGGTTCT[C/T]ATTAGCATTAAAAAA | 55120 |
| rs539733771 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58198859 | CGGTGAAACCTCGCC[C/T]CTACTAAAAAATACA | 55120 |
| rs539745418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192699 | ACTCCTCATTATCTA[C/T]GGTGGAATTTAGTAG | 55120 |
| rs539756273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217820 | AAATCATTAAACATA[C/T]TGGATATCTGACACA | 55120 |
| rs539756742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199246 | AGCGTTGTGTCAGCT[C/G]CTGAAGTTATGATTT | 55120 |
| rs539765981 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236148 | AAGCTCCACAGACCT[C/T]ACGGAGGAAAAACAT | 55120 |
| rs539794965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206267 | TACATTAGCTAAATT[A/C]TTTTTCATTAATCAG | 55120 |
| rs539801877 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58166590 | CATGAAACAATGTGG[-/T]TATGTTTAAAAGATA | 55120 |
| rs539831809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223229 | CTCCTAGAAGACAAA[A/G]TATATGCTGCCTTTT | 55120 |
| rs539853095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174643 | CATTCAAAGCAGTGT[A/G]TAGAGGGAAATTTAT | 55120 |
| rs539952779 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58177793 | AAAATAAAAAAGATT[A/G]AAAAAAAAAGAAAAA | 55120 |
| rs540006327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188983 | CTCCAAGTAATTCTG[A/C]CAAGGAAAAAAGACT | 55120 |
| rs540014070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180324 | TGAAACCAACCCAAA[C/T]GCCCATCAATGATAG | 55120 |
| rs540018963 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235809 | GAGACAGGAAAGATG[G/T]AAATAAAGACTCCCT | 55120 |
| rs540064609 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158941 | ACTTCTCAGTTGCCA[C/T]GGAATCAGAAGGTAA | 55120 |
| rs540068492 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58230900 | AGAACATCATAACTC[-/CTT]CTTGAATGCATACCA | 55120 |
| rs540113571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203209 | GTGTGTGAGAGAATT[A/G]GTCATTTCTCAACCT | 55120 |
| rs540151860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203667 | AAAAAACCCCAGCCA[A/C]AGCAAACAAACTATA | 55120 |
| rs540171209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195835 | ACTTATACAACAATC[A/T]AGGGAAGGCAATTTG | 55120 |
| rs540174313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58179949 | AAGAACACATTTATG[C/T]GGCCAACAAACATAT | 55120 |
| rs540178820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185934 | AAAAACATATTAGTA[C/T]CTATCACTGAAATAT | 55120 |
| rs540268144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202444 | TATATGAAAGCTAAG[C/G]TAAATTGAGAAATAA | 55120 |
| rs540280108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209728 | TGAAAAAATGTGACT[G/T]AAAGAGATTAAGTTT | 55120 |
| rs540298537 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58196959 | TAAAAAAAGGGACAT[A/G]GGTCTCATGAAATTT | 55120 |
| rs540355517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184503 | AGTGAAGATCCAAAA[A/C]TTACAACCAGAACTT | 55120 |
| rs540401147 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242072 | AAGAAACCTACTAAA[A/G]TATTTACCATATGAT | 55120 |
| rs540410593 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58173661 | TGGAAAGGAACAACC[A/G]GTACCAGCCGCTGCA | 55120 |
| rs540438325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236404 | TGGAATCCTAATATT[A/T]CGTTAAGGCAGACCA | 55120 |
| rs540471676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178221 | AAAAATGACTCCTCC[C/G]TAACTCATTTTATGA | 55120 |
| rs540513650 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207132 | AGCACAAGTGATGTG[C/T]GCTTTTGGGGGTTCA | 55120 |
| rs540597198 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58174010 | TGATAAAACAGACTT[G/T]AAACCAACAAAGATC | 55120 |
| rs540608827 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58169934 | TATGTTTGATTGGTG[G/T]GCCTGAAAGTGATGG | 55120 |
| rs540611200 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198801 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGGT | 55120 |
| rs540622534 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58194450 | AAAGTAGAATAAAAT[G/T]ATGAGATGTTCTCAT | 55120 |
| rs540646925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164453 | ATTTACTATGAACAG[A/G]AATTTCTTATTAGCC | 55120 |
| rs540646952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170353 | ATAGATCTTGTCACC[A/C]CCAGGCCTGCCTTAC | 55120 |
| rs540663201 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188386 | CTATCACAGGACCTT[G/T]GCAGCCTTTGCACAT | 55120 |
| rs540725158 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166445 | TTCCACATTTAACTT[C/T]TAGCCAATCTCTGAA | 55120 |
| rs540775158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163278 | GTGAACCGAGATCGC[A/G]CCATTACACTACATA | 55120 |
| rs540790086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177740 | TACATATGTAAGTAA[C/T]CTGCACATTGTGCAC | 55120 |
| rs540810741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221015 | CAGGAGATCGAGACC[A/G]ATCCTGGCTAACACG | 55120 |
| rs540840412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168990 | TCTCCCTGGGACAGA[A/G]CACGTGGGGAAAGGG | 55120 |
| rs540913021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194950 | AAGAAAAATAAAGAT[C/G]TTCCAAGTTTAAAGT | 55120 |
| rs540942227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58220245 | CTTAATCAGGGAGGC[A/G]GTAAGGAAAACGGTA | 55120 |
| rs541007360 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58177074 | TGCAAATCAAAACCA[C/T]AACGAGATATCATCT | 55120 |
| rs541043275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234554 | AATTGGAGATCTTGG[A/G]AAGAAAAATAAAATA | 55120 |
| rs541098836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58200314 | GCTCTGCTAACTAAG[C/T]TGTATGATCCTGAAC | 55120 |
| rs541103458 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58227161 | TAGGGGAGCATACAG[A/T]CGGGCAGGCTGTGGA | 55120 |
| rs541112698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208028 | GGCACCACTGCACTC[C/T]GGCCTTGGTGAAAGA | 55120 |
| rs541133676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193986 | ACTAATGGATAATGC[C/T]CCCTGCTATGTAATA | 55120 |
| rs541160458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58192952 | TTAAAAAATCAATAG[C/T]TTGCCCACATCCTGA | 55120 |
| rs541209988 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238572 | TGAAAGACACAAACT[A/C]CCAAAGCTCACTCAA | 55120 |
| rs541238187 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58219927 | TCCAAACATAAAATC[C/T]CTACTGCATATCTTA | 55120 |
| rs541246215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239079 | GCCACTTCATAAATA[C/T]AGAAATGACAAGAGT | 55120 |
| rs541276085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207656 | AGAGACTATTTGTAT[C/G]AATTTATGACAGAAA | 55120 |
| rs541304666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205930 | TAACTTTTCAGTTAA[A/C]AATATTTATGTAGTC | 55120 |
| rs541342792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213392 | GACCTAATTTAAGAG[G/T]TAAGCCATAAAAATA | 55120 |
| rs541365953 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58184817 | GTCCTGACCTTAAAA[A/T]GTCCCCCAAAACGGG | 55120 |
| rs541393474 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183792 | GCAAAAAAATACATT[A/G]AAGTTGATTCAATGA | 55120 |
| rs541413119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226539 | TCAAAGAGGTTCCTT[C/T]GAACAGTTATGTCCC | 55120 |
| rs541416979 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58176497 | TACAACTACCTGATC[G/T]TTGACAAACCTGAGA | 55120 |
| rs541438160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175724 | CTTTGAAAACCAGCA[A/G]GACAGGGATGCCCTC | 55120 |
| rs541438695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58181706 | CAAATTTAGATGGTG[A/G]ATACATGGGTATTCA | 55120 |
| rs541452128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219659 | CACAGGAGAACAAAA[C/G]TCAGGTAAGATTAGC | 55120 |
| rs541470035 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58212121 | ATTGGGCAATTTACA[A/G]AAGAAAGAGGTTTAA | 55120 |
| rs541530740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186312 | GCCATAAGTATGATT[C/G]GTATATTTGGACCCT | 55120 |
| rs541533876 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58211614 | AAATTTTTTGAACTT[C/T]TATTTTATGCTGTTT | 55120 |
| rs541552531 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58201871 | TCCAGAATAAATAGA[A/G]CAAATGCATTTATTT | 55120 |
| rs541590481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185639 | AGTCAAAGACCCCGA[A/T]AATTAAGCAGGGTAA | 55120 |
| rs541676853 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58236473 | CTAGTTAAAAAAAAA[-/C]ACACACACACACACA | 55120 |
| rs541712194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190845 | TCTATCTAATAAATT[C/G]GTTTGGCTTCTAAAA | 55120 |
| rs541713091 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212049 | AATGCCCCACTCTAC[C/T]GGTACCAATTTACTG | 55120 |
| rs541727008 | snp | A/G | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198608 | CCTGAGGTGTCCAGG[A/G]GGCACAAAATGGAAC | 55120 |
| rs541750857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58191577 | TTTTCATTAATCATC[C/T]CTATTTCATTTTTGA | 55120 |
| rs541751100 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185122 | GGGAAATATTCCCTG[A/C]TATGGAATCTAATCT | 55120 |
| rs541795075 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58167562 | TTTTTTCCAATGGCA[C/T]TGTCCATTTCTCTTA | 55120 |
| rs541807928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166160 | CGTATGCAATAGTAA[G/T]GAGTACAAGATGTAT | 55120 |
| rs541823228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171795 | GCGCGAGCAGAAGCA[C/G]GACGAGGCACTGCCT | 55120 |
| rs541858058 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58172094 | GAAAACAAAGCAGCC[C/G/T]GGAAGCTCGAACTGG | 55120 |
| rs541891521 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240278 | TTTTAACCTCTACTT[C/T]CTGTGATGGTCATAT | 55120 |
| rs541938344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203838 | TTCTACATGTTACAT[A/G]TAGGATGTTACAAAA | 55120 |
| rs541969497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171241 | AACTGCACAACTACA[C/T]AGAAACTGAACAACC | 55120 |
| rs542002757 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58224698 | TTTTTATATAAACTA[A/T]CAACACATAGACAGG | 55120 |
| rs542006141 | snp | C/T | 0.000675514 | 0.0183658 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165835 | CCTTTAGTGATTCTA[C/T]TGCTGCCAAAAACTG | 55120 |
| rs542010887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180089 | AGATGCTGAAGAGGA[G/T]GTGGAGAAATAGGAA | 55120 |
| rs542024239 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178614 | TTTATGACAAACCCA[-/C]AGTCAATATCATACT | 55120 |
| rs542043750 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58224675 | TGTTAGCAATATTAG[A/T]ATTGTAATTTTTATA | 55120 |
| rs542046052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231185 | GTTGGTACGCCCCAA[A/G]GTCTTGTCACTGGCT | 55120 |
| rs542101634 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58198985 | AGTGAGCCGAGACTG[A/C]GCCACTGCACTCCAG | 55120 |
| rs542103511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237879 | AAGAGATTAAAGAGA[A/C]TGTGCATCTTTATTG | 55120 |
| rs542152857 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | FANCL | GRCh38.p7 | 2:58174079 | ATCAATTCAACAAGA[A/G]GAGCTAACTATCCTA | 55120 |
| rs542157426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178928 | TCACAAGCATTCTTA[C/T]ACACCAATAACAGAC | 55120 |
| rs542160975 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170502 | TAACCAGCTAGCATC[A/G]TAATGACAGGATCAA | 55120 |
| rs542203236 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243029 | CTTTATTTTGCAACT[C/T]GGTAATTAAGGACGG | 55120 |
| rs542271307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235661 | CTGCAAAGAAGCAAG[A/G]CAATACCCACAATGA | 55120 |
| rs542290549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222298 | AATATTCTCCTGGAC[C/T]ATTATGCCTATCGGA | 55120 |
| rs542325969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58211052 | TTCTCACAGCTACAC[C/T]AGGCGGTGCCTCAGT | 55120 |
| rs542326600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204376 | ATGCCAACCCTTTCT[C/G]CTGCTATAGATTTAC | 55120 |
| rs542381915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174544 | AGAATGACTACTGGG[C/T]ACATAACAAAATGAA | 55120 |
| rs542395849 | snp | C/G | 0.000181988 | 0.00953734 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241252 | TCATACACGGTTTTC[C/G]ACCGGTTCTGGGGCA | 55120 |
| rs542432682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235368 | CAGCCAGAGTGGAAA[C/T]CTTGCAATGTAAGAG | 55120 |
| rs542432841 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241445 | TGGAGGATTCCGCGG[A/G]CGGAAATGAAGGTGA | 55120 |
| rs542434596 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182333 | TCAAGTGATTCTAAT[G/T]TGCAGATAAGGTTAA | 55120 |
| rs542443635 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164364 | AAAAGAGGTCATTAA[C/G]AGAAAAAAATGACTA | 55120 |
| rs542465630 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58173529 | GAATTTCATATCCAG[A/C]CAAACTAAGCTTCAT | 55120 |
| rs542575390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202401 | CTAAAAAAAAAAATT[A/G]TCACATCTCAAAGAC | 55120 |
| rs542586650 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58186259 | CAAATAATCAAAAAG[A/C/T]AAACATCAGAATTTT | 55120 |
| rs542601656 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163673 | TAATGGTAAATATAA[C/T]TGAACCAAAAGAAGT | 55120 |
| rs542629449 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209269 | ACAATGTAGAGGATG[C/T]TGTCAGACTGGTTCA | 55120 |
| rs542639898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229735 | GTTACAACATTGTGC[A/C]AAGCAGGTCTTTAAA | 55120 |
| rs542750821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58182425 | CACACTTCCATACAA[C/T]TCACAAAAAGAAAGG | 55120 |
| rs542765584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188952 | AACTATATTACATGC[C/T]ACAACATGGTTGAAT | 55120 |
| rs542772201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58187541 | TGCACGTTGTGCACA[C/T]GTACCCTAAAACTTA | 55120 |
| rs542791123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161827 | CAATTCTTCTAACTA[C/T]TTTAGAATACGAAAT | 55120 |
| rs542791630 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FANCL | GRCh38.p7 | 2:58177656 | GGAGGGGGGAGGGAT[A/G]GCTTTAGGAGATATA | 55120 |
| rs542798703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195041 | AATTATCTGAAATCT[A/G]TTTACCATCTCTTAA | 55120 |
| rs542829961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164884 | CTATACTTTCTTCTC[A/G]TAATACCACGTATGT | 55120 |
| rs542884053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227653 | TATATTTCTCTCAAC[A/G]TCCAGCCACTTGTGT | 55120 |
| rs542897143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193875 | ATACGAACTGAGGCA[A/C]AGGGCAGTTATGTGA | 55120 |
| rs542933630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58194422 | ATATATTTTGAAGCA[C/T]TTGTGATGTTAGAAA | 55120 |
| rs543029154 | snp | C/G | 0.000438813 | 0.0148059 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163118 | ATTGCATGCTCTACT[C/G]TTGGTTTCTAAAGCC | 55120 |
| rs543035139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168910 | CCAGATTCCTCCTCT[C/T]TGGGCAGGGCACCTC | 55120 |
| rs543051606 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58189909 | ATAATACTTGCAGAT[-/AA]AAATCCCCTAATAAT | 55120 |
| rs543053978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169502 | ACACCTTTTCTCCAA[C/T]GGATCACAACTCCTC | 55120 |
| rs543116362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221335 | TTCAGAAACTGAATA[C/G]CAAACAAATCATCAC | 55120 |
| rs543158395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172895 | AAACTTTGAAAAAAA[C/T]TTAGACGAATGCATA | 55120 |
| rs543159845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207549 | ACCTCTGAATTGTTA[A/G]ATGAGAGATGAATAA | 55120 |
| rs543166971 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58181822 | AAATGATATAAATTA[C/T]GTATGAGTTATTTGT | 55120 |
| rs543188018 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180479 | ACCAAACACTGCATG[C/T]TCTCACTCATAAGCT | 55120 |
| rs543201171 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227303 | TAGTCAGCTCAATTA[A/C/G]ACCCCTGCCTTATTG | 55120 |
| rs543224120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172560 | GTTAACAGAGGGTCT[A/G]TTTGTTAACAGAAAG | 55120 |
| rs543266747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233548 | TAAGAATAAATAAAA[C/T]CACAAAAATCCCATG | 55120 |
| rs543295895 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213537 | TATTTTTAAACAGTA[G/T]AAAACAAATGATTAA | 55120 |
| rs543296581 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164687 | TTAATCATAACCTGA[G/T]AATTACTTTAATGGG | 55120 |
| rs543323179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226473 | GAGTACATTTTATTT[C/T]TTCACCACCTGCCCA | 55120 |
| rs543335277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196436 | TCAGTATATTCCACA[A/G]ATTAAGAATTTATAA | 55120 |
| rs543369751 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58171589 | ATGAACCCAGGAGCT[-/G]GTTTTTTGAAAAGAG | 55120 |
| rs543390475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58180960 | TGAACTCTCATATAC[C/T]GTCAGTGCGCATGTA | 55120 |
| rs543397162 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239598 | TTTGAAATATGGACT[C/T]TATCTTAGATAATAG | 55120 |
| rs543426712 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168867 | GCTCACCGCAGCTCA[A/G]CAAAGCCTCTGTAGC | 55120 |
| rs543465332 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190815 | TTACAAACTCCAATA[C/T]TTTCCAATTCTATAT | 55120 |
| rs543472833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238512 | TTATTGTAAATAACT[G/T]TAAGCCAATAAAATC | 55120 |
| rs543498571 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188136 | CTTACAGATATCTAA[C/T]TGTCTCAGCACCATG | 55120 |
| rs543510538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199235 | TGAATTAAGTCAGCG[C/T]TGTGTCAGCTGCTGA | 55120 |
| rs543537373 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221659 | CAAACATGGAAAATT[C/T]AGAATACAGTTGTAT | 55120 |
| rs543557039 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58214969 | TTGCACTTCTCTCAA[A/C]CATGTCAGATCCACT | 55120 |
| rs543594856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161791 | TCACCTCAACATTTA[A/C]CTTTTATGTTGGGAA | 55120 |
| rs543597574 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 2:58243609 | GTTGGCTCCTTGATT[C/T]GGAATCCCCATAATT | 55120 |
| rs543617379 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58189619 | CACTTAAGCAGGAAA[A/G]TATGAACACTGCCAA | 55120 |
| rs543631899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238133 | CCAACACAAATTAAT[A/G]AACTTTCTTAAAACA | 55120 |
| rs543655226 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214099 | AGAAATTAAATAAGA[A/C]TACATGAAGCACCTA | 55120 |
| rs543675644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167415 | ATCTCTGTTTCTCCT[G/T]TCTCTGTCTGTTTCT | 55120 |
| rs543686571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212524 | AAAGCATAAATTAGG[G/T]CTGTCCTAGGCAAAA | 55120 |
| rs543699531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180553 | CACACACCAGGGCCT[A/G]TCGGGGGGTGGGGGA | 55120 |
| rs543703108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205877 | AAACCAAATTATAAA[A/C]AATAAAACTGCATTA | 55120 |
| rs543714025 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243366 | ATTATTTACTAAATA[C/T]CTTAATTTGGGTTGT | 55120 |
| rs543719663 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193605 | GGCAACAGTAAGACT[A/G]CCAACAAAGAAAAAG | 55120 |
| rs543748690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219553 | TACGGTGCAGAAACC[C/T]GACAAATACTACCTC | 55120 |
| rs543797229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224629 | AAAATGGTCTCAACA[A/G]GGATCACAAAGAAAT | 55120 |
| rs543797551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217356 | GCAAAGATGTGCTCC[C/T]TCTGGAGGCTCTAGG | 55120 |
| rs543832891 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58225710 | TGCCAGATTACAAAG[A/T]AAGTAGAATATGTTA | 55120 |
| rs543833738 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58237596 | ACATAAAAATAATAG[-/A]AAAAAAATTGAAGAA | 55120 |
| rs543883155 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58185702 | TAAATGAAATAAACC[A/C]CTCGAAAACTGGGTA | 55120 |
| rs543915969 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58191710 | ATATGTGTGTATAAA[G/T]CCACAAATATACAAT | 55120 |
| rs543918242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198522 | GAAATAATCCCCCCA[C/T]GGATACTCTGGGACA | 55120 |
| rs543919188 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219901 | GTGCTATTATCATAC[A/G]ATGGAAGACATCCAA | 55120 |
| rs543975704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161119 | CAGCCTGAAAAGTAA[C/T]AGATACTACATAGTA | 55120 |
| rs543979784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166997 | GGTGCGCAGATCACG[A/G]GGTCAAGAGATAGAG | 55120 |
| rs544074688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197709 | CTCAAAATATTGAAT[A/G]TTCTAAAGCACAAAA | 55120 |
| rs544084308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196372 | ACATTTGTCAAATCT[C/G]AGTTGTGATAAAAGG | 55120 |
| rs544102746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58205182 | TTTTTAATATCACTA[C/T]ATGCCATTTAGATAC | 55120 |
| rs544123428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196997 | ATAAAAAAAGAAAGC[C/T]ATAAAATTTATGCAT | 55120 |
| rs544174163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171715 | CATTTCCATCTGAGG[A/T]ACCGGGTTCATCTCA | 55120 |
| rs544196800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175033 | AAACTAGAAAATCTA[A/G]AAGAAATGGATAAAT | 55120 |
| rs544234144 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58175329 | GGGCAGAGACACAAC[A/C]AAAAAAGAGAATTTT | 55120 |
| rs544236206 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171401 | AAGGGAAATTTATAA[C/G]GAAATGCCCACATGA | 55120 |
| rs544240791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172910 | TTTAGACGAATGCAT[A/G]ACTAGAATAACCAAT | 55120 |
| rs544262868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165156 | CAGCCATTTTATAGT[C/T]GAGAACATGATAACA | 55120 |
| rs544294307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185015 | TGGGGTAGGACTGCA[C/G]GAGAAAAAAGAGGCA | 55120 |
| rs544326269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179549 | GCAGAAAACTCAAAC[A/G]GGACCCCTCCCTTAC | 55120 |
| rs544346654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209812 | GAATGAATTTAGTAT[C/G]AACAAGGATCTCCAT | 55120 |
| rs544370708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58178873 | TAAGCTGATAAGCAA[C/T]ATCAGCAAGGTCTCA | 55120 |
| rs544385444 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58175789 | TCTGGCCAGGGCAAT[C/T]AGGCAGGAGAAGGAA | 55120 |
| rs544387142 | in-del | -/A | 0.331179 | 0.236453 | intron-variant | FANCL | GRCh38.p7 | 2:58215704 | CTGCTATTAAGTGGC[-/A]AAAAAAAAAAAAAAG | 55120 |
| rs544393543 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201284 | CATATCATATAGGAA[A/T]ATTAACTGAAAAATA | 55120 |
| rs544411107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174050 | AAAGAAGGCCATTAC[A/G]TAATGGTAAAGGGAT | 55120 |
| rs544411286 | in-del | -/T | 0.496308 | 0.0428067 | intron-variant | FANCL | GRCh38.p7 | 2:58228072 | TAACAATATGGTCAT[-/T]TTTTTTTATTTTTCC | 55120 |
| rs544425912 | snp | C/T | 0.000281278 | 0.0118558 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160112 | AATTTGCTTACCTTA[C/T]TACAATATGGACATT | 55120 |
| rs544556993 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242675 | ACCATGCTTTGTCCA[A/G]CCGTACTTCCCCACA | 55120 |
| rs544640206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203770 | TTTATAGTAACAGCT[A/G]AATGCAAAAGATTTT | 55120 |
| rs544652602 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196517 | CTTGTATGACCCAAT[G/T]AAACCTGAAACTTAA | 55120 |
| rs544655782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235280 | GGAAAACACCCAAAG[A/G]TGGGAACGTACAGGA | 55120 |
| rs544659546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164309 | TAAGCCTTTCACTAA[A/G]GCTGGCATCAACATA | 55120 |
| rs544668125 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211678 | AAGTCACCTCTTCAA[C/T]GTTTTGCTGCTTAGA | 55120 |
| rs544743506 | snp | C/G | 1.66222e-05 | 0.00288285 | intron-variant | FANCL | GRCh38.p7 | 2:58241212 | AAGCAACCACTGGGC[C/G]GGTACCTGAGCCGAG | 55120 |
| rs544763003 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222393 | ATGATGTTTGATATA[C/T]ACATTTTTTAAAAAG | 55120 |
| rs544787182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163710 | GATATGATTATCATT[A/G]AAAGGATCTTAAATT | 55120 |
| rs544812031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222158 | ATAAAAGTGCCTGTT[C/T]TTTTACGGAAATCTG | 55120 |
| rs544845795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58228772 | GTTCTACCTAACCAA[C/T]TGGGGGGCAAGGAAA | 55120 |
| rs544857257 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169482 | GGAAAATTCCAAAAA[A/C]CAGAACACCTTTTCT | 55120 |
| rs544880009 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58201383 | ATAACTAAAAAAAAA[-/G]ATTACATAATATTAA | 55120 |
| rs544893936 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220244 | TCTTAATCAGGGAGG[C/T]GGTAAGGAAAACGGT | 55120 |
| rs544939898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213924 | GGTAGTTGGGGAGAA[A/T]TTATTAAAGGCTCCA | 55120 |
| rs544990076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227592 | TGCTCTTGACATGCT[C/T]TCGATGTCCTCTCGA | 55120 |
| rs545003764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235620 | TGTCTAGCATCCAAT[C/G]AAGATATACCAAGCA | 55120 |
| rs545017217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173235 | ATTATCCAGGAGAAC[G/T]TCCCCAATCTAGCAA | 55120 |
| rs545039630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228208 | AAAATGGCAAAAAAG[A/G]AAATAATCTCTAAAG | 55120 |
| rs545084971 | snp | G/T | 0.000167378 | 0.00914664 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159769 | GTATTCTTATTTCAG[G/T]GTTTCCTTCCAGACA | 55120 |
| rs545110191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194472 | TGTTCTCATCGTCTA[A/T]GCTAAAATCTATAAA | 55120 |
| rs545147000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194967 | TCCAAGTTTAAAGTC[C/T]AGAAACACTGACTCC | 55120 |
| rs545169775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187143 | CGGCATGATTCACAA[C/T]AGCAAAGACTTGGAA | 55120 |
| rs545190743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240636 | CTACACATGTGTTAG[C/T]ATGTGTAATAAACTC | 55120 |
| rs545203004 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187899 | AATTCTCTTAATAGT[A/G]TCTTTCAAGAACAGA | 55120 |
| rs545207229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169758 | ACTTTGTGAAGCATA[C/T]ACAAGTATCAATTGC | 55120 |
| rs545231552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193850 | GGTTCACCATTTCCA[C/T]ATACAGTACATACGA | 55120 |
| rs545284680 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58233317 | TATTTGCAAAGCCCA[A/G]CCATTTTAAAAGGTC | 55120 |
| rs545392161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177083 | AAACCACAACGAGAT[A/G]TCATCTCACACCACT | 55120 |
| rs545392838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173006 | CAGAAGCCTCAGGAG[A/C]CGATGCGATCAACTG | 55120 |
| rs545459860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172533 | CCAACAGACCTGCAG[A/C]TGAGGGTCTCTGTTA | 55120 |
| rs545498114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58168202 | TCTGCAGCTCCCAGC[A/G]AGATCAAGGCAGAAG | 55120 |
| rs545537398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176454 | TCAATGGAACAGAAC[A/T]GAGCCCTCAGAAATA | 55120 |
| rs545543132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219519 | TAAAGTGTGGAGAGA[C/G]AGAAAAAAACAGTAA | 55120 |
| rs545544569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58186772 | GTAAAGTGGCGGAAC[C/T]GCAGTGAATTGTTTT | 55120 |
| rs545581855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212484 | CAAACTGGGACATAT[G/T]TGAGACTGACAGGGG | 55120 |
| rs545596840 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FANCL | GRCh38.p7 | 2:58175815 | AGGAAATAAAGGGTA[C/T]TCAATTAGGAAAAGA | 55120 |
| rs545671052 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183564 | GTTTTGTTCTCACTC[C/T]GCTTCATTGATTTTA | 55120 |
| rs545681179 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231440 | CTTAGAGATCTGAGC[C/T]GGGAATTTGAAAAGC | 55120 |
| rs545706125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193081 | TTAAGAAATCATTGC[C/T]ACTTTACTGAAGGAC | 55120 |
| rs545721301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180142 | GTGTAAATTAGTTCA[A/T]CCATTGTGGAAGACA | 55120 |
| rs545722247 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58239141 | AATAGTCGACTCAAG[C/G]AAAAGTCAATGGACG | 55120 |
| rs545757445 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168316 | GAGCCAAAGCAGGGT[G/T]GGCTATCACCTCACT | 55120 |
| rs545762577 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162500 | ACTTATACACAGATT[A/T]TTTTTTTAACCAAAT | 55120 |
| rs545769009 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232922 | AAAAGTAATAAAATT[C/G]TCAAAAAACAATTAC | 55120 |
| rs545803153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161050 | CTCAGATCACAAAAG[A/G]CATTCTTCTCAACAT | 55120 |
| rs545893447 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237914 | CTCTGTTGTATCATA[C/T]ACTCAGGAGAAGCTA | 55120 |
| rs545926923 | snp | C/G | 0.029116 | 0.117091 | intron-variant | FANCL | GRCh38.p7 | 2:58172171 | CCACCTCTGGGGACA[C/G]GGCACAGACAAACAA | 55120 |
| rs545977786 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58218835 | CTACATATGGTAATG[A/G]ACTGGAGTTGTAGAC | 55120 |
| rs546007758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225506 | GGCTAAAATCATTAG[G/T]TGACAGTCTGATGGG | 55120 |
| rs546070581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231746 | AGTTGGAAAAAAAGT[G/T]TTCTAATCCTTTTGT | 55120 |
| rs546072194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224724 | ACAGGAAAAGCATAA[C/G]TGAAATATAACAAGT | 55120 |
| rs546086936 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221878 | AAACTGCTAAAACTA[A/G]AAATACATTAAGTTA | 55120 |
| rs546095327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58171679 | CCCAGGGTGAGCGAC[A/G]CAGAAGACGGGTGAT | 55120 |
| rs546130196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211465 | GTGAAGACCTCTGGC[A/G]TGCCCTGGAGACATT | 55120 |
| rs546130688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58191619 | TCCTTGTTTACTGCA[C/T]GTAAATAAAATGCTG | 55120 |
| rs546135116 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58201270 | AACAACAAAAGCTCC[A/C]TATCATATAGGAATA | 55120 |
| rs546159368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58238046 | AATAGCTATGTGAAT[A/G]AGCAATCTTGGAAGC | 55120 |
| rs546230709 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58225235 | AGATACTTTAAAAAA[A/G]AAAACACTTTAGATC | 55120 |
| rs546233190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231296 | CACACACATCTGCAC[A/T]CCAGGTCTCACACTC | 55120 |
| rs546248029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170177 | AGCCCATCAGACTAA[C/T]AGCAGATCTCTCTGC | 55120 |
| rs546255325 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201788 | TCTAGTCAAAATAGG[-/T]TATTTGTTTTCTTTG | 55120 |
| rs546294012 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58200016 | CAATATACACTCTGA[A/C]TAATGGAATCTGGCT | 55120 |
| rs546294078 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58227707 | GGGTTTTTATAGGCA[C/G/T]AAGATGGAGGTATGG | 55120 |
| rs546294704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205141 | TTGGAGTTCAGAATA[C/T]AAGCCTCCTAACTTA | 55120 |
| rs546306810 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58197122 | CTATTTTGCTATGTT[G/T]TCTCAACTTCCATTG | 55120 |
| rs546320436 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 2:58243580 | CTGGACAGTGTGACC[A/C]CTTGCCAAAAGCAGT | 55120 |
| rs546331952 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58214957 | TGATTTTTCTTATTG[A/C]ACTTCTCTCAACCAT | 55120 |
| rs546358861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171305 | TTAAGGCAGAAATAA[A/G]TAAGTTTTTTGAAAC | 55120 |
| rs546407450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173905 | AAATCTCACAAGCAG[A/G]GACACACATAGGCTC | 55120 |
| rs546440730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217087 | ATCCAGAATACAGGA[C/G]TTTGAAAAAAATACA | 55120 |
| rs546475835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211161 | CCCTGCAGCAAACTT[A/C]TGCCTGGGCATCCAG | 55120 |
| rs546507900 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179800 | AACAGGCAATCTACA[C/T]AATGGGAGAATATTT | 55120 |
| rs546533330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235402 | TTAAATAGAGTGCTC[A/C]GAAGGTGTTGCTTCA | 55120 |
| rs546541064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174187 | CCCACACAATAATAA[C/T]GGGAGAATTTAACAC | 55120 |
| rs546555031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187895 | TTCTAATTCTCTTAA[C/T]AGTGTCTTTCAAGAA | 55120 |
| rs546557919 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199392 | AATAGGCAGTATCAG[A/T]TAAAGGAATTAAGAA | 55120 |
| rs546565592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58215635 | CTCAATATATTTATC[A/T]ATTCTGGCACAGGGC | 55120 |
| rs546588789 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231883 | TTTAGTAACAGGTAA[A/T]TATTTACAAATGCTG | 55120 |
| rs546594831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234949 | AGACATTAAACAATA[C/G]GCAGCGAGGACAGTG | 55120 |
| rs546609250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209406 | ACTACTAGATAATTT[C/G]CAGTTATTCAATGAC | 55120 |
| rs546640886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240859 | AACATCCGTGGAGGT[A/G]GAGGGTGTTAAAATC | 55120 |
| rs546643351 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178055 | GAAGAAGTCAAATCC[C/T]GAAATAGATCGATAA | 55120 |
| rs546664141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200712 | ATAGTAAATGGTATC[A/C]ATGTCCTGATATGGA | 55120 |
| rs546669213 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58174529 | TGAACAACCTGCTCC[A/T]GAATGACTACTGGGT | 55120 |
| rs546709552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178392 | TCTACCACGATCAAG[C/T]TGGTTTCAACCCTAG | 55120 |
| rs546746162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178939 | CTTATACACCAATAA[C/T]AGACAAACAGAGAGA | 55120 |
| rs546816794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207874 | CCAGCCTGGGCGACA[C/G]AGTGAGACCTCATCT | 55120 |
| rs546845119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173049 | TCAGTGACGGAAGAT[A/G]AAGTGAATGAAATGA | 55120 |
| rs546848816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195292 | TACCATCCAAAGTCC[C/T]TATGATATACAGCCA | 55120 |
| rs546882336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181883 | TTCTGGATTAGGTTA[C/T]AGACTAATTTGCTTC | 55120 |
| rs546930755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220589 | ATGTTTAAGTCTCTA[C/T]TTAGTTTTTCTTTAG | 55120 |
| rs546931969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182760 | CCTAATACAATTCAA[G/T]ACAGCAACTCTGAAT | 55120 |
| rs546965909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58169334 | GTTAGACGGAAAACT[A/G]ACAAACAGAAAGCAA | 55120 |
| rs546977526 | snp | A/C/T | 6.67763e-05 | 0.00577793 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241290 | GGGGCACTGGCGCAA[A/C/T]AGGCTCGCTTCCGTC | 55120 |
| rs547008795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177242 | TCCTCAGGGATCTAG[C/G]ACTAGAAATACCATT | 55120 |
| rs547080110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169527 | CTCCTCGCCAGCAAG[A/G]GAACAAAACTGGACA | 55120 |
| rs547104367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58186942 | GAGGATGTGGAGAAA[C/T]AGGAATGCTTTTACA | 55120 |
| rs547156854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169538 | CAAGGGAACAAAACT[A/G]GACAGAGAATGAGTT | 55120 |
| rs547175651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162599 | GCCGACTTCTTCTAT[A/G]TATGGGTCCTGCAGG | 55120 |
| rs547176749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173296 | AGAGAATGCCACAAA[A/G]ATACTCTCGAGAAGA | 55120 |
| rs547220139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169209 | CTTCCAGAGAAAGGA[A/T]CAGGCAGCAAAATCT | 55120 |
| rs547231825 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58240627 | TTCAAAACCCTACAC[-/AT]GTGTTAGTATGTGTA | 55120 |
| rs547265982 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58176847 | AGTGAACAGGCAACC[C/T]ACAAAATGGGAGAAC | 55120 |
| rs547280388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239320 | TCACAAGCCTTGAGA[A/C]GGACAAAACAATCTT | 55120 |
| rs547327957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167851 | CTTAGCAATTTCAAC[A/G]AACTTAGGGGGTAGA | 55120 |
| rs547396270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233636 | TATGAAGCACTTTCC[A/G]ATAGAACCTACTCTA | 55120 |
| rs547431006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227429 | ATTAAGTGCAAGTAG[C/T]TCTCAGTAGATGTGG | 55120 |
| rs547437978 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58176071 | GGAATCCAACTTACA[A/G]GGGATGTGAAGGACC | 55120 |
| rs547537942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238878 | CTTTTAAAACACTGA[C/T]GAGAGGAAATGCAAA | 55120 |
| rs547557449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232855 | ACTTGAGCAAAAATA[C/G]CAGAAAAAGACAAAC | 55120 |
| rs547592477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162196 | TACCATTTAGTAGTC[C/T]ACAACCTTAGCAGCC | 55120 |
| rs547609561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192640 | AGTTATTTGGGGAAA[G/T]CAGGAAGATAGGATG | 55120 |
| rs547640236 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238166 | TGGGATTTTTTGTGA[-/T]TTTTTTTTTAGCTTA | 55120 |
| rs547677667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206212 | TTAAGAAACAGTAAA[A/G]CTAATGGAAAAATAA | 55120 |
| rs547723908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231077 | AAGCCTCTCTTTATT[A/T]GGCTTGAAAGACTCT | 55120 |
| rs547725823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238172 | TTTTTTGTGATTTTT[C/T]TTTAGCTTATCAGCT | 55120 |
| rs547786494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237601 | AAAAATAATAGAAAA[A/G]AATTGAAGAAATTAA | 55120 |
| rs547788941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58191734 | ATACAATATCATTAC[A/T]CATGGAGAGAGACTA | 55120 |
| rs547825207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161227 | TAACAAGGAATTTAT[A/G]GAAAGATTCCAATGT | 55120 |
| rs547863813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180265 | CTACTATAAAGACAT[A/G]CATACATATGTTTAT | 55120 |
| rs547905433 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180468 | GTGAACAGAAAACCA[A/G]ACACTGCATGTTCTC | 55120 |
| rs547937413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180573 | GGGGTGGGGGACTAG[A/G]TGAGGGATAGTATTA | 55120 |
| rs548109262 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58191444 | CACAATATATTAACC[A/G]ATAAAACTGTGAAAC | 55120 |
| rs548134441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190304 | GGGTATCTGCCCACA[A/G]GACCAAATGAAACAT | 55120 |
| rs548135775 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243139 | AGTCCCTTACTTCAA[A/G]CACTTTATAATTTAT | 55120 |
| rs548156055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160640 | TTAATTTTCAACCCA[C/T]TGATTATAAGCATGA | 55120 |
| rs548175196 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58195577 | AGAAGGATGTGACCA[A/G]ACTGAAAGTTAAACT | 55120 |
| rs548209509 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222634 | TGCTAGGCCTATCTA[A/T]GAAGGCTTTAAAATG | 55120 |
| rs548211051 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214820 | ACCTGGCCCATGAGG[A/C]ATCTTAAGTCTTGCC | 55120 |
| rs548269316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204705 | GCTGGTATTTGTTCA[C/T]ATACTCAAATTGATC | 55120 |
| rs548273956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229434 | TTATTTCTGCCACAT[C/T]TTTTCTGTTGCTAAT | 55120 |
| rs548293292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189265 | TACTGTATGTCAATT[A/G]TATCTCAATAAAGCT | 55120 |
| rs548297879 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58166111 | GGTTTTTTAAAAATC[A/G]TAATTTTTTTATTAT | 55120 |
| rs548340509 | in-del | -/TCTA | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58237656 | TAAAATTTATAAACC[-/TCTA]TCTAGATGTATCGGG | 55120 |
| rs548342383 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58171437 | CAGAAAGAACTAAAA[C/T]TGACACCCTAACATC | 55120 |
| rs548344350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166044 | CATCTCTTCCTACAG[C/T]GTTTACAGGATTCTT | 55120 |
| rs548348077 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58170479 | AGAAACTGCATCAAC[A/T]AACAAAATAACCAGC | 55120 |
| rs548438229 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58194247 | CAAAACCGCAATTTT[C/T]ACATCCATTTTTGCT | 55120 |
| rs548468712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58164707 | ACTTTAATGGGGCCA[C/T]GAAAATAATGATTTA | 55120 |
| rs548489193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179316 | GCTGGAAGCATCATG[C/T]TACCTGACTTCAAAC | 55120 |
| rs548509922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170117 | AAATGAAGGAAAAAA[C/T]GTTAAGGGCAGCCAG | 55120 |
| rs548535806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173471 | GCCAGAAGAGAGTGG[A/G]AGCCAATATTCAACA | 55120 |
| rs548568046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58179937 | GACATTTCTCAAAAG[A/G]ACACATTTATGCGGC | 55120 |
| rs548571503 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58173781 | GATCAAACTCACACA[A/T]AACAATATTAACTTT | 55120 |
| rs548586619 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58230070 | ATTTCAAAATATAAA[A/T]AACTGCAATCAGTAA | 55120 |
| rs548603770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202778 | AACTAAATGTCATCA[A/G]CTTGGATTAAAATCT | 55120 |
| rs548613360 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159152 | ATTATATCCAGATTT[C/G]CTTGTTGGATGTTTA | 55120 |
| rs548626431 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180934 | AAATGTTAATAAGGA[C/T]ACAAAGCAACTGAAC | 55120 |
| rs548729394 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229266 | TTATGTCATTATTTT[C/G]CTTCAGTAACTGATT | 55120 |
| rs548766150 | snp | A/C | 0.000113841 | 0.00754372 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241349 | ACAGAAAAGCTCTAG[A/C]CCTGCTGGGTCCTGC | 55120 |
| rs548776954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165269 | TTTCTCTGTGCTTTC[A/T]GTTTACTCTTCAGTG | 55120 |
| rs548783293 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169668 | TGAAAAAAAGTTAGA[A/G]GAATTGCTAACTAAA | 55120 |
| rs548796160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58182652 | CATATTCAACAAAGT[A/G]TATGAGTCAAGCACT | 55120 |
| rs548809103 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241694 | AGCCTGGACGTTGTA[C/G]CACTCTGTCTTCTTT | 55120 |
| rs548832663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177856 | GCCAGACTAATAAAG[A/G]AGAAAAGAGAGAAGA | 55120 |
| rs548908917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209931 | AAAACCTACCAATAT[A/G]TGTTGACAATCTCCC | 55120 |
| rs548911589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233877 | AGGAGAAAAGATAGG[G/T]AGAGACACCTTTTGG | 55120 |
| rs548928579 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58178330 | CAGTGTGAAAATCCT[A/C]AACAAAATACTGGCA | 55120 |
| rs548974790 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58240177 | GTCTACAAGAGAATC[A/G]TATTTTCAGCTAGGT | 55120 |
| rs549033902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214835 | AATCTTAAGTCTTGC[C/G]TTATGTATCCTTAGT | 55120 |
| rs549109787 | snp | G/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162748 | GATGCAGATCAGAAG[G/T]CTGTGTTATAATATT | 55120 |
| rs549118784 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58181017 | TGACAATTTCTTTAA[A/G]AACTAAATATATTCC | 55120 |
| rs549152479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187802 | CGTCCATTTTGAGTT[C/T]TATTATTGAACTTTG | 55120 |
| rs549212813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163860 | TCACATGTTTAAGAA[A/G]TAACTATCTAAATTA | 55120 |
| rs549239716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58201708 | ATATACCTATAAAAA[A/C]CAAAAAATTTATCTG | 55120 |
| rs549259872 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215455 | AATAGCTTGCTAAAG[A/G]CCAACACTTCTACAG | 55120 |
| rs549271716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176653 | ATTAAAGACTTAAAC[A/G]TTAGACCTAAAACCA | 55120 |
| rs549315764 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58187402 | AAGGAACATCACACA[C/T]TGGGGCCTGTCGTGG | 55120 |
| rs549320270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58186435 | TATGGGGAAAATTTA[C/T]TGGAAGTGAACTCAG | 55120 |
| rs549367060 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58204467 | TGTGTCAAGGCTCAT[-/G]GCTGTGGTCAGTGAG | 55120 |
| rs549369760 | snp | A/T | 0.000732936 | 0.0191293 | intron-variant | FANCL | GRCh38.p7 | 2:58226828 | ATTTGCACAATAAAT[A/T]TTCTATCCACTAAAA | 55120 |
| rs549372745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169123 | AGACTGCCTCCTCAA[A/G]CAGGGGTCAAAAGAC | 55120 |
| rs549386387 | in-del | -/T | 0.138207 | 0.223612 | intron-variant | FANCL | GRCh38.p7 | 2:58227885 | CAACCTCATCATTAC[-/T]TTTTTTTAAAGAAGA | 55120 |
| rs549420320 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176879 | TTTTCGCAACCTACT[C/T]ATCTGACAAAGGGCT | 55120 |
| rs549423576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207247 | TAGCAAAGATCATGA[C/G]GACAGGAACAACACT | 55120 |
| rs549432942 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58181345 | ATATCTGGAATAGAC[A/G]TAACTAAGCTTTGGT | 55120 |
| rs549454177 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58177189 | CTGTTGGTGGGACTG[G/T]AAACTAGTTCAACCC | 55120 |
| rs549454393 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238016 | AGAGCAGTAACAAAC[C/T]GAGGCCTCATGGCCA | 55120 |
| rs549535599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173036 | GGAAGAAAGGGTATC[A/C]GTGACGGAAGATGAA | 55120 |
| rs549536877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232704 | TTAACTATATATTTG[A/G]ACAAACAGAATTTTA | 55120 |
| rs549538428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172228 | TAAATGTCCCTGTCC[A/G]ACAGCTTTGAAGAGA | 55120 |
| rs549563646 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162056 | GGCAAGATGTTTGGG[C/T]ATCAGTAATATTCCC | 55120 |
| rs549590407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198804 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG | 55120 |
| rs549637282 | in-del | -/ATT | 0.000644762 | 0.0179434 | cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163510 | TATATTTATGGAAAC[-/ATT]ATTACCTAGAATGAA | 55120 |
| rs549642312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180639 | TGCAGCAAACCACCA[C/T]GGCACGTGTATACCT | 55120 |
| rs549663452 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58175509 | AAATGTAATCCAGCA[C/T]ATAAACAGAACCAAA | 55120 |
| rs549719035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167832 | TGGACATAGAAACAC[A/T]TCTCTTAGCAATTTC | 55120 |
| rs549738165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58232272 | ATATATGCAACACAA[C/T]ATTGCATTTGAGGGA | 55120 |
| rs549750120 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238305 | TGGCAAATATCTTGA[C/T]TGCAAGATCATGAGA | 55120 |
| rs549752373 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58206194 | AATGGACGTGAAAGA[A/G]GTTTAAGAAACAGTA | 55120 |
| rs549809453 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58215275 | TCTCTCCTCACCATT[C/G]TTATGCTTAATTTTA | 55120 |
| rs549903431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224778 | ACAATGATGTTAACA[C/T]TAGAAAACAGCATTT | 55120 |
| rs549922075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167230 | AGAAAAAAAAGGTGT[A/G]AAGTAGGAATTAGAG | 55120 |
| rs549931661 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166213 | TTAATGTACATGATA[C/T]AGCTAACATTGGACC | 55120 |
| rs549948009 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237483 | AAAGAAAATTTAAAG[A/C]ACTAAATATCTGTAC | 55120 |
| rs549964849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231414 | TTTTCCATCTGTGAC[C/G]TCTTCTCTAGCTTAG | 55120 |
| rs549978672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160500 | AAATAATGCATACTA[A/C]GTTCCTGGCATTCAT | 55120 |
| rs549979196 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58209233 | GTATGTGTCAGTGTA[-/C]CCATGTTCCATGTAT | 55120 |
| rs550054198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205503 | TCTGAAGTTCAGATA[C/T]ATCAATACCTGACTC | 55120 |
| rs550069570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211802 | TAAAACATAACAAGA[A/G]TAACCTTTGCTCCAG | 55120 |
| rs550105753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212198 | GGAAGGCAAAGAGGA[C/G]CAAGTCCCATCTTAC | 55120 |
| rs550110742 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243009 | GGGGCAGGACATAAC[A/G]CCTGCTTTATTTTGC | 55120 |
| rs550154442 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58202240 | TATACCTTTTTCCTA[-/A]AAAAAAAAAAAAAAA | 55120 |
| rs550177681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204631 | TTTAATGCTCCCTTT[G/T]TTTTTCTCCTCAATG | 55120 |
| rs550195741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217566 | AGTTATAACAAAGTA[A/G]ACATTAAGACAAGAA | 55120 |
| rs550216926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216671 | TATTAGGGATGCCAA[A/T]ATATAAGATCATATG | 55120 |
| rs550221915 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234918 | ATTGGACAAAACATA[A/T]GAAACAATGATTTTC | 55120 |
| rs550230385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58218239 | AAAAAAATCAATGAC[C/T]TACATATCCATCTCA | 55120 |
| rs550253364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166469 | CTCTGAATTCAGCAT[G/T]TCATATATTAATCCC | 55120 |
| rs550257348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236553 | AATAATATAAAATAC[A/T]GAAAAATACCAAAAC | 55120 |
| rs550357993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222584 | TAAGTCGGAGTATTA[A/T]GCCATCCATCTGGCT | 55120 |
| rs550369588 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225064 | TGAACCTGGGGCAAC[C/T]GGTATCAGAAGGCAA | 55120 |
| rs550434228 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183283 | CAAACTCTTAAGTTT[A/G]GAGATTATTTCACTA | 55120 |
| rs550439005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170554 | AGCTAAATCCCCCAA[C/T]TAAAAGACACAGACT | 55120 |
| rs550456964 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164795 | CCATAATTTGGTTAA[C/T]TGTTCCAAATTAAAC | 55120 |
| rs550466020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196645 | GACTTTCCAGTCTAG[C/T]AGAGAGTCACAAACT | 55120 |
| rs550502647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197225 | ATATAATTAAAATGG[A/C]ATTTTGGCCTTGACA | 55120 |
| rs550502944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190501 | GCCAAGCCAATTAGT[A/G]GACCAGAAAAAAAGA | 55120 |
| rs550528947 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58199355 | CCTAAATTTAATTTC[A/C]AATAGCATCAGTCAC | 55120 |
| rs550532294 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58227442 | AGCTCTCAGTAGATG[G/T]GGGAGACAGAAGGGA | 55120 |
| rs550544168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210735 | CAGCCATTCCAAATG[G/T]GAGGAATTGGCCAAA | 55120 |
| rs550561052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170444 | AACATACGAAAATGT[A/G]AAGACCATCAACACT | 55120 |
| rs550583948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183373 | CTGAATTCTCCAAAG[C/T]AGCTTTTCCATCATT | 55120 |
| rs550597735 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191764 | ACTTCTTTGCCCATA[C/T]TAGCTCTCACTATAT | 55120 |
| rs550606283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196006 | TGTGAATAACCTTAT[C/T]AGTAGTGCTACAGAT | 55120 |
| rs550622333 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172244 | ACAGCTTTGAAGAGA[A/G]CAGTGGTTCTCTCAG | 55120 |
| rs550669560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195396 | AATCAGCCCCCAACC[C/T]GCACAAATGAAGAAG | 55120 |
| rs550685734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235431 | CACTTGTAGAGACTA[A/C]CTACCTTAGACTAAA | 55120 |
| rs550695300 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58174304 | TAATAGAAATCTACA[C/G]AACTTTCCACCCCAA | 55120 |
| rs550727668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174677 | ACTAAATGCCCACAA[A/G]AGAAAGCAGCAAAGA | 55120 |
| rs550730823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173696 | CATGCCAAATTGTAA[A/C]GACCATCGAGGCTAG | 55120 |
| rs550742498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188612 | CACCCAGCTGATTTT[G/T]GTATTTTTTGTAGAG | 55120 |
| rs550758172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178961 | ACAGAGAGACAAATT[A/G]TGAGTGAACTCCCAT | 55120 |
| rs550762243 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238396 | AGACAATAATTGTTT[C/T]TGTTTTAAGCCACTA | 55120 |
| rs550794247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202045 | TTAACATACAGTTAA[C/T]GTTTCAACTATTAGT | 55120 |
| rs550834091 | snp | C/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58189084 | CATCAGTAGTTGCCT[C/G]AGGCCCTGGTGGAAG | 55120 |
| rs550867008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169620 | TGAGCTAAAGGAGCA[C/T]GTTCTAACCCAATGC | 55120 |
| rs550894226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173375 | GAAAAAATGTTAAGG[G/T]CAGCCAGAGAGAAAG | 55120 |
| rs550918960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58177350 | TGTTTATTGCAGCAC[C/T]ATTCACAACAGCAAA | 55120 |
| rs550949000 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58214255 | TTTTGGCTTTCATCT[A/G]TTATCGAAGTTAGAA | 55120 |
| rs550951510 | snp | A/G | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158850 | AGCTTTCCAAGAGAC[A/G]TAACACTATAGCTAC | 55120 |
| rs550974644 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159063 | ATTCAGTTTTCATAT[C/T]CTATCCTATTTATTT | 55120 |
| rs550975079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58236060 | AGGAACAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 55120 |
| rs550989811 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198140 | AATGGACATTAACTG[C/T]AAGGAAATATAAAAG | 55120 |
| rs551099546 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58164511 | CAGACAGTACTTTCA[C/G]GTAATATGGGCATAT | 55120 |
| rs551116752 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181101 | AATACCGTTACCGGA[A/G]TGCTCACAGCAGCTA | 55120 |
| rs551142193 | snp | A/C/G | 3.41338e-05 | 0.00413107 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241309 | CTCGCTTCCGTCACC[A/C/G]CCATGGCTCGAAGTC | 55120 |
| rs551146891 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58214761 | AAGTGATCTGCCCCA[C/T]CTCAGCCCCCCAAAG | 55120 |
| rs551161092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169994 | TTCAGGATGTTATCC[A/G]GGACAGCTTCTCCAA | 55120 |
| rs551176076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187291 | GAAGCTGGAAACTAT[C/T]ATTCTCAGCAAACTA | 55120 |
| rs551180825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163299 | ACACTACATACTGGG[A/C]AACAAGAGCAAAACT | 55120 |
| rs551184632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209175 | AGCTTGCCAAACACA[C/T]AATAAACTTTTTAAT | 55120 |
| rs551217634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162712 | GTACTTAACAACCAA[A/T]CAAAGGTAAACAAGT | 55120 |
| rs551290131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233757 | AAAAAATAGTAACAA[C/G]CTCTGGTAAATCAGA | 55120 |
| rs551345739 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58182560 | ACAATAAATTTGTAA[A/G]AAATAAAACCCATTT | 55120 |
| rs551375595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220734 | CAAAAGGCCAACTCA[C/T]AGAAAATAGCTAAAA | 55120 |
| rs551375617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227881 | TCTAACAACCTCATC[A/G]TTACTTTTTTTAAAG | 55120 |
| rs551416905 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58178016 | AATTCCTGGACACAT[-/A]ACACCCTCCCAAGAC | 55120 |
| rs551476116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212691 | AACAACATGGGCAGA[A/G]GTTAACAGAAACCCA | 55120 |
| rs551490689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168485 | CTGGTGCCTATTTCA[A/C]CAGGGCCCTGGGTTT | 55120 |
| rs551540912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226127 | AAAAAGTAGAAGAGG[A/C]AATAAGATTGGCAAA | 55120 |
| rs551644269 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184249 | TTTACTCTTTGATCA[A/G]AATAATTTTCACATC | 55120 |
| rs551650902 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58194006 | GCTATGTAATAGGAC[A/T]GACTCCTTTAATTAC | 55120 |
| rs551671211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58199632 | GACAAACCAAGTTTT[C/T]AAGTTAACAAAGGCA | 55120 |
| rs551698494 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58169071 | CTGAAAAGAGCAGCA[G/T]ATCTCCCACCACAAC | 55120 |
| rs551702535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239383 | GAATTTAATAGTGAG[A/G]AAATATCATCCAAAC | 55120 |
| rs551708573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193568 | TTTGATCCCTTTGAT[A/G]TCTTTTCAGCCATAC | 55120 |
| rs551708891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200605 | GTATTTGGAGTAGAT[A/G]CACAAAGTAAAGTAT | 55120 |
| rs551750540 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204741 | AGGAAAATGCTGTAT[A/G]AGCACAGGTACAGCC | 55120 |
| rs551759827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231461 | TTTGAAAAGCATCCT[C/T]TATTCCTTTTTCCCT | 55120 |
| rs551802921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58198735 | GTATTTTAGAAAAAC[G/T]AGATGTATTAGGGGC | 55120 |
| rs551807224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212335 | GGGGAAACTGCCCCC[A/G]TGATTAAATTATCTT | 55120 |
| rs551811877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58186368 | ATACAACAATGACAA[C/T]TGGCCCAAGCTTGAG | 55120 |
| rs551828597 | snp | A/G | 1.68635e-05 | 0.0029037 | intron-variant | FANCL | GRCh38.p7 | 2:58232119 | GTCTCTTCCCTGTGG[A/G]AAATATTGAAAAGGA | 55120 |
| rs551829131 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58197306 | TATTTACTTTACTCA[G/T]GTATTTATGTTTTAA | 55120 |
| rs551840486 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162045 | CATTTTTGGCTGGCA[A/G]GATGTTTGGGCATCA | 55120 |
| rs551865949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58198091 | TGGGTGTGAGTGGGT[A/G]TGTTTGTGTGTGCAT | 55120 |
| rs551881718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172322 | TTCTTGACCCCTGAC[C/G]CCTGAGCAGCCTAAC | 55120 |
| rs551901054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58176142 | AGAGGATACAAACAA[A/G]TGGAAGAACATTCCA | 55120 |
| rs551901837 | in-del | -/AATTTA | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58197945 | TACAGAGTTCTTTGG[-/AATTTA]AATTTAAAGGAAAAT | 55120 |
| rs551920722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175461 | GGGCTTCATCCCTGG[A/G]ATGCAAGGCTGGTTC | 55120 |
| rs551962355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180607 | GAAATACCTAATGTA[G/T]ATGTCGGGTTGATGG | 55120 |
| rs552049568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179666 | AAACCATTCAGTACA[C/T]TGGCATGGGCAAAGA | 55120 |
| rs552051393 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202687 | TCTTATCTACCTTGA[A/G]AAAGTATAGAAAAAA | 55120 |
| rs552091635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171879 | GTGACAGACAGCACC[C/T]GGAAAATCGGGTCAC | 55120 |
| rs552112416 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58179385 | CTGGTACCAAAACAG[A/G]GATATAGACCAATGG | 55120 |
| rs552115090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238256 | CCCAGGGAAGCCAAA[A/G]GATTGGACACCCTGT | 55120 |
| rs552115805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211701 | TGCTTAGAAATTTCT[C/T]CCACCAGATACCCTA | 55120 |
| rs552185034 | snp | C/G | 0 | 0 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161949 | AATATAATTACATTA[C/G]TATTTAACACCTAGC | 55120 |
| rs552280618 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58227307 | CAGCTCAATTAGACC[A/C]CTGCCTTATTGCAAG | 55120 |
| rs552316091 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58171591 | GAACCCAGGAGCTGG[C/T]TTTTTGAAAAGAGTA | 55120 |
| rs552331424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165942 | ATAATCTTTTACTTA[A/C]AATACACTCAATTTA | 55120 |
| rs552331597 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226562 | TATGTCCCTCATGCA[C/G]TTCAAGAAATGCGTC | 55120 |
| rs552335433 | snp | C/T | 1.67125e-05 | 0.00289067 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159732 | ATAATTTTTTAAGTT[C/T]CCAGCTCTTCACCGA | 55120 |
| rs552338561 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58211313 | CAGCCACGGCCCAAG[C/T]TCTACACTGGCCCTT | 55120 |
| rs552344087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167168 | AGTGGGCCGAGATCG[C/T]GCCACTGCACTCCAG | 55120 |
| rs552357079 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186568 | CAGCTGTAGAAAAAG[C/T]TCCTCAGAATTCCTG | 55120 |
| rs552403517 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58217508 | TAAAAAAATGCAAAT[C/G]GTAAAGAGCAGTTTT | 55120 |
| rs552407158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166724 | ATCTGAAATAACTGG[C/G]CACACCAATAATTTA | 55120 |
| rs552428803 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58237326 | AACAAAAAGATATCT[A/T]GAAAATCCTTAATAT | 55120 |
| rs552442634 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58217788 | GCTCTCAGGACAAGC[A/G]GACAAAAAAAAAAAA | 55120 |
| rs552473467 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58175143 | TGTGGCGAAAATCAA[C/T]AGCTTACCAACCAAA | 55120 |
| rs552519774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164286 | GATAAATTCCATACA[A/C]TGTAGAATAAGCCTT | 55120 |
| rs552541826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58189450 | AGAAGAGTTCATACA[A/C]CCAACACTTAAAAGA | 55120 |
| rs552585496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58223594 | AGCAGAGAAGCAACA[C/T]ATTCTTCACAGAAAA | 55120 |
| rs552585760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230912 | CTCCTTCTTGAATGC[A/G]TACCATTCTCTAACC | 55120 |
| rs552604469 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214625 | AGTGATCCTCCCACC[G/T]CAGCCTCCCGAGAAG | 55120 |
| rs552621474 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58224265 | TCTCCTTGTATTTGT[A/G]TTGTTTATTAAAATT | 55120 |
| rs552644863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169436 | ACGTAGATAAATCCA[C/T]GACGATGAGGAAAAA | 55120 |
| rs552645671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58241130 | CCCACAAGTCTGGGC[A/C]CCTAACCTCCTAGCC | 55120 |
| rs552701686 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242389 | TCACCTGGGAACTAT[A/G]TAGAAATACAAGTTT | 55120 |
| rs552704552 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233092 | GAAACAAAATGTACT[A/G]CTGACCTTTTCAAAA | 55120 |
| rs552735401 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58198011 | GAAAATGAAGCATAA[A/C]TATCTACAGGCTGGA | 55120 |
| rs552754124 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58191384 | GAATATTTTACTGAG[-/T]TTACTCCAAACCATA | 55120 |
| rs552832192 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58165311 | TGCAAGTTCTTTTAT[C/T]TTCCTCTGTATTTCT | 55120 |
| rs552860113 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233705 | TCAGGAAAAAAAATG[C/T]ATGGGAGAGAGACTG | 55120 |
| rs552912682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233946 | TAGGCTCTTATACGA[A/G]TAAATAAAAAAACAA | 55120 |
| rs552916751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58227162 | AGGGGAGCATACAGA[C/T]GGGCAGGCTGTGGAG | 55120 |
| rs552955572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58227557 | TCAATGGCCTGCCGG[C/T]ATGCTGAAGTCTATC | 55120 |
| rs553001675 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202153 | ATATTCCTATATGTG[C/G]AGTTTTTGTTGTTGT | 55120 |
| rs553013264 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58177416 | ACTGGATTAAGAAAA[C/T]GTGGCACATATACAC | 55120 |
| rs553056869 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58208778 | CTTTACTTCGTCTCT[A/G]TACACCAATCCATTC | 55120 |
| rs553063181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169739 | TGAAAAACACAGCAC[A/G]AGAACTTTGTGAAGC | 55120 |
| rs553147194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214434 | TACCCTTCTTATCGT[G/T]GTCATAATTCAGTAT | 55120 |
| rs553149730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207330 | CTGCACTGTTTAAAA[C/T]GGTAGCCACCAGCCA | 55120 |
| rs553220244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208053 | GAAAGACAGAGACCA[C/T]GTCACTAAATTTTTT | 55120 |
| rs553257664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58203737 | GATCACAGATAAGAA[C/T]AAGAACTACAAAAGA | 55120 |
| rs553287804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182255 | ACAAATTCTATTCCA[C/T]CCATTCCTTTTTAAT | 55120 |
| rs553328060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199985 | CAATAATAAGTTGGC[C/T]AAAAAGATTTACTAT | 55120 |
| rs553366392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212454 | ACCATATCATAAAGT[A/G]ATATGTATTTCTTCC | 55120 |
| rs553383773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172469 | TGTTCTGCAGCCACC[A/G]CTACTGGTACCCAGG | 55120 |
| rs553427854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186548 | GTCAATGGTAGCTAT[A/G]TAAGCAGCTGTAGAA | 55120 |
| rs553429774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180437 | ACACGGATGAAGCTA[C/G]AAACCATCATTCTCA | 55120 |
| rs553443028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176315 | AAAAAAGAGCCCGCA[G/T]CGCCAAGTCAATCCT | 55120 |
| rs553443669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194281 | TCAGTGACCTGGACA[A/G]AAGGAATTTCGTTTT | 55120 |
| rs553448919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181708 | AATTTAGATGGTGGA[A/T]ACATGGGTATTCACC | 55120 |
| rs553466759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180810 | TTGTTTAAAGGTTTT[C/T]TGTGTGTGTGTGCCC | 55120 |
| rs553467423 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58219504 | GTGACTTCCAAAGAG[C/T]AAAGTGTGGAGAGAG | 55120 |
| rs553485043 | snp | C/G/T | 0.0170251 | 0.090679 | intron-variant | FANCL | GRCh38.p7 | 2:58179506 | TCCCTATTTATTAAA[C/G/T]GGTGTTGGGAAAACT | 55120 |
| rs553514236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187125 | GCACACATATGTTTA[C/T]TGCGGCATGATTCAC | 55120 |
| rs553529396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58199015 | GCCTGGGCGACAGAG[C/T]GAATCTCCATCTCAA | 55120 |
| rs553591101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186152 | GTGCAGCCTTTGATT[C/T]ATAAATTGATTTTAA | 55120 |
| rs553599336 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206929 | GTTGAGTATATGCGA[C/T]CTTGATTGTCAATTG | 55120 |
| rs553599985 | snp | A/G | 1.65761e-05 | 0.00287885 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162961 | CCCTGAAAGCATGGG[A/G]AAAAAAATTATGCTG | 55120 |
| rs553620090 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184022 | GGTGACTTCCAGGTA[A/T]AGAAGTCAAGAATTC | 55120 |
| rs553657353 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58210924 | TTGCAGGGTATGGCA[A/C]CCCCACCCGGCTGAG | 55120 |
| rs553659651 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167118 | TTGGGAGACAGAGGC[A/T]GGAGAATCACTTGAA | 55120 |
| rs553732017 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58168164 | TGGTGGCTGGCAAGA[A/T]GGCCAAACAGGAACA | 55120 |
| rs553742734 | snp | A/C/T | 0.000120578 | 0.00776384 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161629 | AAATTCCACAATCCA[A/C/T]AGTAAAATCCTTCAA | 55120 |
| rs553783651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192125 | TACCAATGAAGGCAT[C/T]TGATTAAAAAAACCT | 55120 |
| rs553841055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171252 | TACATAGAAACTGAA[A/C]AACCTTCTCCTGAAT | 55120 |
| rs553849625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175774 | CATAGTGTTGGAAGT[G/T]CTGGCCAGGGCAATT | 55120 |
| rs553878049 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58171676 | GCTCCCAGGGTGAGC[A/G]ACGCAGAAGACGGGT | 55120 |
| rs553966596 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | FANCL | GRCh38.p7 | 2:58175261 | TCAATAGAAAAAGAG[A/G]GAATCCTCCCTAACT | 55120 |
| rs554050310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224525 | TAATCAAAGTCCTAC[C/T]TTAGAAGGTTCTTAT | 55120 |
| rs554085451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217800 | AGCGGACAAAAAAAA[A/T]AAATAAATCATTAAA | 55120 |
| rs554103653 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180242 | TACCCAAAGAATTAT[A/G]AATCATGCTACTATA | 55120 |
| rs554108203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229742 | CATTGTGCAAAGCAG[A/G]TCTTTAAAGAACAAT | 55120 |
| rs554274060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236373 | TATAGTTGATAAACC[A/G]ATAGTGCATAAAAAA | 55120 |
| rs554279321 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202757 | TCTGAATACTGCCAA[C/T]AAATGAACTAAATGT | 55120 |
| rs554291694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, synonymous-codon, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160048 | ATATAGATCTATCTT[C/T]TAGAACATATTACTG | 55120 |
| rs554298850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175000 | ATCAGAGAATACTAT[A/C]AACACCTCTATGCAA | 55120 |
| rs554315964 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58228445 | TATTACAGATGATCA[A/G]TAAATGACAGGGTCT | 55120 |
| rs554317625 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58216971 | TTTTTAAATATTTTT[A/T]AAAAATTATTTAACC | 55120 |
| rs554318297 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242118 | TTTTCCAATTTTCCA[A/G]TGCATCACGTTTGAG | 55120 |
| rs554319183 | in-del | -/A/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58213716 | TGTCTCTTAAAAAAG[-/A/AA]AAAAAAAAAAAAAAA | 55120 |
| rs554404796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215979 | TGAGACAAAGTCTCA[A/G]TGAATACCCCAGGAT | 55120 |
| rs554404993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209529 | TACAAAAAATTATCA[C/T]TATTGGTTGTAATTA | 55120 |
| rs554466416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179511 | ATTTATTAAACGGTG[C/T]TGGGAAAACTGGCTA | 55120 |
| rs554481647 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | FANCL | GRCh38.p7 | 2:58184906 | AGTACATTCTACTTC[C/G]CCTTCCACAAAAGGT | 55120 |
| rs554489177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223857 | TTCTGAATAAGTTCA[A/G]TAACTACTGATTTCA | 55120 |
| rs554504795 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210124 | TTCTGAATTATCTAG[A/G]AACATATGATTATTA | 55120 |
| rs554568131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58215159 | TCCATCAATCTATAC[C/T]TAAAGAATGACTAGG | 55120 |
| rs554576691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186766 | AAAGAAGTAAAGTGG[C/G]GGAACCGCAGTGAAT | 55120 |
| rs554594189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174361 | CACCACACCACACCT[A/G]TTCCAAAATCGACCA | 55120 |
| rs554611936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196309 | ACATTTTATTTTTAA[A/G]ACAAAGAGAAATATA | 55120 |
| rs554640748 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221281 | CACTTAATAATAAAT[A/G]TAATGTTTCAAAGTA | 55120 |
| rs554642455 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241953 | CAAAACATGAGTAAA[C/G]ATTGCTGATGGACTT | 55120 |
| rs554708697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58189775 | ATTTCCAGTATTTTA[A/G]TAATTTCCACAAAGT | 55120 |
| rs554716862 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58218061 | ATCTCCAGTTGTTTG[A/C]AAATTAAGAGATATA | 55120 |
| rs554733480 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178615 | TTATGACAAACCCAC[A/T]GTCAATATCATACTG | 55120 |
| rs554741207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183048 | AAATGTATAAAAATT[A/G]GGAGCCATTATTATA | 55120 |
| rs554770259 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58170703 | GGAAAGCAAAAAAAA[A/C]AAAAAGCATGGTTTG | 55120 |
| rs554780994 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188149 | AATTGTCTCAGCACC[A/T]TGTGTTGAAAGACTG | 55120 |
| rs554783468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58178190 | GTACCATTCCTTCTG[A/G]AACTATTTCAAACAG | 55120 |
| rs554804581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221436 | TTTATGCATCAGTTT[A/T]AAAAAAAAAATCATT | 55120 |
| rs554806865 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58165600 | CAAAAAAAAGTTTAT[A/C]CTAGAAAATTTTAAT | 55120 |
| rs554807573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194423 | TATATTTTGAAGCAT[C/T]TGTGATGTTAGAAAG | 55120 |
| rs554838435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173968 | AAATGGAAAACAAAA[A/T]AAGGCAGGGGTTGCA | 55120 |
| rs554900273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58178620 | ACAAACCCACAGTCA[A/G]TATCATACTGAATGG | 55120 |
| rs554905304 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169352 | AAACAGAAAGCAATA[G/T]CATCAACATCAACAA | 55120 |
| rs554942567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169687 | TTGCTAACTAAAATA[A/C]CCAGGTTATAGAAGA | 55120 |
| rs554960290 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219705 | TCCTATATCCAGCAT[A/G]GCTCTAAAAAGTGTG | 55120 |
| rs554978359 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178423 | GATTCAAGGCTGGTT[C/T]AACATAAGCAAATCA | 55120 |
| rs555034008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172901 | TGAAAAAAATTTAGA[C/T]GAATGCATAACTAGA | 55120 |
| rs555071525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58173106 | AGAATAACAAGAAAC[A/G]AACAAAGCCTCCAAG | 55120 |
| rs555085150 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58228527 | AAGTTTTATTGGCAT[A/G]TAGCCATACACATTC | 55120 |
| rs555167245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235066 | TGGACAAACAAATAA[A/G]AGCATAATATTCTCC | 55120 |
| rs555209390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202092 | CGCAGGCCCAATTTC[C/T]TTTTTTTTCCCTAAA | 55120 |
| rs555215460 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236641 | CCATATGAATAACCA[C/T]GTTAAATGTAAATAG | 55120 |
| rs555281351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164258 | GATTTCATTTTCATC[A/G]TAAAAATGTCTTGAT | 55120 |
| rs555297857 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192040 | ACAGTGGCTGAGCAG[A/G]TATGAAGCCTACTGT | 55120 |
| rs555299159 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58169635 | TGTTCTAACCCAATG[A/C]AAGGAAGCTAAGAAC | 55120 |
| rs555330865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58241009 | GCTCCACGCCGCGCG[C/G]CTCCTCGCTCCCCAT | 55120 |
| rs555350181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233077 | GTCCTTTAAAAAAAT[A/G]AAACAAAATGTACTA | 55120 |
| rs555423339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227157 | CCTCTAGGGGAGCAT[A/G]CAGACGGGCAGGCTG | 55120 |
| rs555463720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213798 | ATCTTTCACAAATCT[A/G]CGCAACAGATTTTGA | 55120 |
| rs555473319 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58164512 | AGACAGTACTTTCAC[A/G]TAATATGGGCATATT | 55120 |
| rs555523824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227528 | CCTGGTCGAACTCCA[A/C]GTCATTCTGCCGGTC | 55120 |
| rs555543811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198960 | CGTGAACCTGGGAGG[C/T]GGAGATGGCAGTGAG | 55120 |
| rs555711024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206421 | TATGGGAGACTGCTT[C/T]TCTTTATAAGCCTTA | 55120 |
| rs555757548 | snp | A/G | 0.000450161 | 0.0149959 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162838 | TATGCAATACTGTCT[A/G]GAATATCAAAACACT | 55120 |
| rs555762586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58218494 | TTTTTTAAAATGAAC[A/G]TAGGATGAAACAGAG | 55120 |
| rs555835500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199784 | AAAAGCTAAATGTAC[G/T]GAAAGAAAATTAGTT | 55120 |
| rs555838959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58180413 | GATGAGTTCATGTCC[A/T]TTGCAGGGACACGGA | 55120 |
| rs555862065 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200286 | ACAGAGACCTCAGCT[C/T]TCTTTGGTTCCAGCT | 55120 |
| rs555873870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225269 | GTGACAGTTGCTAGG[C/T]ACCAACTCATTATTC | 55120 |
| rs555892604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58167419 | CTGTTTCTCCTTTCT[C/T]TGTCTGTTTCTACAT | 55120 |
| rs555893973 | in-del | -/AATAAG | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58184579 | GTGCATACATACAAT[-/AATAAG]AATAAGGAAATGAAT | 55120 |
| rs555902152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192934 | TGATCAAAATAAAAC[A/G]TTTTAAAAAATCAAT | 55120 |
| rs555951074 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58169160 | TACAGGAGAGCTCCA[-/G]CTGGCATCTGGAGGA | 55120 |
| rs555961204 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58172354 | GGGAGGCACCGCCCA[C/G]TAGGGGCAGACTGAC | 55120 |
| rs555963783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58211441 | AGGGCTGTTATGTGA[A/G]TGGCTGCCGTGAAGA | 55120 |
| rs555983371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191536 | CACCTTCCACATCCA[C/T]GTAGCCTGGTGAGAT | 55120 |
| rs555998867 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233987 | CCCAGCACTCGCCAA[C/T]ATTTCATCCATTAAA | 55120 |
| rs556002506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58186052 | AGAAAATTTTTCAAA[C/T]AGTGACAAGTCAAAG | 55120 |
| rs556003510 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58166045 | ATCTCTTCCTACAGC[A/G]TTTACAGGATTCTTT | 55120 |
| rs556005793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197017 | AATTTATGCATAATT[C/G]CAATTCTTTAATAGA | 55120 |
| rs556042769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197391 | GTAGCCTCCATTTAC[A/G]GAATATTTGTAAAAT | 55120 |
| rs556086012 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175698 | GAATGGGCAAAAACT[G/T]GAAGCATTCCCTTTG | 55120 |
| rs556099433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171209 | AATTAGAACTCAGGA[A/T]TAAGAAACTCACTCA | 55120 |
| rs556111114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160844 | GCTACCTCTAATCAC[A/C]AAAGTAAAGATGTGA | 55120 |
| rs556122557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172061 | GAGGGGCGCCCGCCA[C/T]TGCCCAGGCTAGCTT | 55120 |
| rs556122841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176217 | GCCCAACGTACTTTA[A/T]AGATTCAATGCCATC | 55120 |
| rs556140648 | in-del | -/AT | 0.0103295 | 0.0711199 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241838 | ACTAAGTTCAATCAG[-/AT]ATATTTGAGGCACAC | 55120 |
| rs556151784 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58204812 | GCTTCTGACACTTAA[C/G]CTATGCATGTATTCA | 55120 |
| rs556201812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236029 | TTGGAGTGCCCAACA[C/G]AGAGGACAGAAAAGG | 55120 |
| rs556203862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185593 | TGCTTTTGGCAATGC[C/T]TGCCAATTTTTATGC | 55120 |
| rs556262569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174956 | ATAAAGGGTACATCA[C/T]CACCGATCCCACAGA | 55120 |
| rs556317263 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58211389 | AGCCTGCACACAGTG[C/G]TGGGACCCTGTGCCC | 55120 |
| rs556363886 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213620 | GCGAACACCTGTTAA[C/T]CCCAGCATTTTGGGA | 55120 |
| rs556399951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58238328 | TCATGAGAGATTTTG[A/G]TCAAGAACTACCATC | 55120 |
| rs556417676 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58166642 | TGATACAAAATCAAA[-/AC]AGTTTAATAAGAAGG | 55120 |
| rs556423102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166139 | TATAATGCTTGATAT[A/G]CTACACGTATGCAAT | 55120 |
| rs556509447 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241865 | CACACACATGTATAC[A/G]TATATGTGTATTGAT | 55120 |
| rs556517428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210945 | CCCGGCTGAGTTCAT[A/G]GGCTGGTGTTGAGTG | 55120 |
| rs556526750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184842 | AACGGGAGGAAACAT[C/T]GTGAGAAAGTTAGGA | 55120 |
| rs556549885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204330 | TGCTATATTCCTATT[A/G]ATCCATTATAAAAAT | 55120 |
| rs556564982 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158781 | GTTTTATATTAATAC[C/T]ACTTAATTTGCTTTA | 55120 |
| rs556568178 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58230533 | TCATCCACTTACTGG[-/C]TGACCTCTGTTGTGC | 55120 |
| rs556653315 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58235645 | CAAGCACATATATTT[A/C]CTGCAAAGAAGCAAG | 55120 |
| rs556655423 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58165452 | GAGTTACCTGTTCCA[A/C]GATTCCTGTGCTAAT | 55120 |
| rs556668971 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181562 | CATGCCGATGACATA[G/T]TTTGAAGAAAGTATT | 55120 |
| rs556670613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58179133 | GGATAGGAAGAATCA[A/G]TATCGTGAAAATGGC | 55120 |
| rs556705954 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180508 | CTGGAGTTGAACAAT[A/G]AGAACACATGGACAC | 55120 |
| rs556786002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203597 | GATTATAGATCACTA[C/T]CCTATAAGGGATCTA | 55120 |
| rs556796680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214449 | GGTCATAATTCAGTA[C/T]TACTATGATCAACTA | 55120 |
| rs556796702 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58221824 | AATAAGGATCAAATA[C/G]TCTAGTTACAATTAA | 55120 |
| rs556816235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223734 | AATAAAATAACCTAC[C/T]ACTTAGGATTATTTT | 55120 |
| rs556816402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216179 | CTTGGAAGCTCTAAA[C/G]GGTTATAGCTTGAGA | 55120 |
| rs556835565 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58238562 | ACAAATTCCTTGAAA[A/G]ACACAAACTACCAAA | 55120 |
| rs556841009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169775 | CAAGTATCAATTGCC[A/G]AATCAATCAAGCGGA | 55120 |
| rs556864927 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58229606 | AGAACCTAAAGTCTC[A/C]AAGATGGAAATCGAT | 55120 |
| rs556873715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208902 | GAATCATTAGCCTCG[C/T]AGTCAAGACCCCTCT | 55120 |
| rs556956012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221307 | AAGTATCCACACTAA[C/G]AAGGAAGCTAAATTC | 55120 |
| rs556956782 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192581 | GGATACAAATATCTT[C/T]ATAATAATGTAAACA | 55120 |
| rs556962180 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58167823 | GTGACAAGTTGGACA[C/T]AGAAACACTTCTCTT | 55120 |
| rs556985914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203003 | ACATGTGACCCTTTG[A/G]AAGGATAAAGGCAAA | 55120 |
| rs557005162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194869 | AGGAAGACAGGGACC[A/C]TAAGGAAAATTACCC | 55120 |
| rs557038346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196256 | GAAAGATGGGAAGGA[A/G]GGACAGAAAAGGGGG | 55120 |
| rs557045697 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192289 | AATCAACTGAAACTA[C/T]AGCGATATAATATCT | 55120 |
| rs557058767 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172929 | AGAATAACCAATACA[C/G]AGAAGTGCTTAAAGC | 55120 |
| rs557097957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58195638 | GACATGCCACAGAGA[C/T]ATTTATATCCCATAT | 55120 |
| rs557127679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200976 | AATCAATTTTGTTTA[G/T]ATAACAAACCTCACA | 55120 |
| rs557145482 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58187432 | GGGTGGGGGGGATGG[C/G]GAAGGGATAGCATTA | 55120 |
| rs557152004 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58209469 | TTATAAAGGTTTTCA[C/G]TTTAACTGAAAACCA | 55120 |
| rs557155054 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58173953 | GAAGATCTACCAAGC[A/C]AATGGAAAACAAAAA | 55120 |
| rs557183970 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58182412 | ATATTACCAGAGTCA[C/G]ACTTCCATACAATTC | 55120 |
| rs557195995 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235868 | AAAATATGCTAGATA[A/G]TATCAACAGCAGATT | 55120 |
| rs557199589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200181 | TTAAAAATATCAGAT[A/G]ATGTGCTTCAGAGTA | 55120 |
| rs557227958 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58173081 | GCAAGAAGGGAAGCT[G/T]AGAGAAAAAAGAATA | 55120 |
| rs557230277 | in-del | -/TAACT | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58198405 | ATTATAATCTAGAGA[-/TAACT]TAAAGTATACAGAAG | 55120 |
| rs557244604 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242250 | CTGAAGATTCTTAAA[A/G]TTTGACAAGAATTTG | 55120 |
| rs557277881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58178065 | AATCCCGAAATAGAT[C/T]GATAACAACTTCTGA | 55120 |
| rs557305496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58228010 | AAATCAGGCAACTCT[A/G]TGTAATTTTTAAAAT | 55120 |
| rs557316444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178498 | CATGATTATCTCAAT[A/T]GATGCAGAAAAGGCC | 55120 |
| rs557418789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176455 | CAATGGAACAGAACA[C/G]AGCCCTCAGAAATAA | 55120 |
| rs557429394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172873 | AAACCAAAGGCGAAG[A/T]AGCTGAAAACTTTGA | 55120 |
| rs557436280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188003 | AAATATCTGCCTAGC[C/G]TAGAGTTACAAATAC | 55120 |
| rs557455294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176901 | CAAAGGGCTAATATC[C/T]AGAATCTACAAAGAA | 55120 |
| rs557467881 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209475 | AGGTTTTCAGTTTAA[C/T]TGAAAACCATACTGG | 55120 |
| rs557562879 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58240354 | TGGGCACAAGGTTGA[A/C/G]TGTAATGGTCAGAAA | 55120 |
| rs557579750 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58180854 | AAAGTAATCAAAAAA[A/G]AAATCGAAACTTTTC | 55120 |
| rs557601436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240953 | GAAGGAAGCCAAACT[C/G]GGGGAAGGGCTAGGG | 55120 |
| rs557647346 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230741 | AAATGTCCATTGGTA[A/G]CCCCTGCTCAAAATG | 55120 |
| rs557652860 | snp | A/T | 0.00229515 | 0.033798 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163096 | ATTAAAAAAAAAAAA[A/T]TTAATAATTGCATGC | 55120 |
| rs557668812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169270 | CCAGGCAAACAAGGT[C/G]TGGAGTGGACCTCCA | 55120 |
| rs557722733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162264 | GGTATCTATTCAATT[C/T]TGAGAAACTATAACT | 55120 |
| rs557759572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161729 | TGTGATATTTTGATA[C/T]ATGTATACAGTGTTT | 55120 |
| rs557774860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186600 | CCAAGAACCAGAATG[C/G]AAGAGCATTTTTTTC | 55120 |
| rs557792542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212495 | ATATTTGAGACTGAC[A/G]GGGGCCAAAACAAAA | 55120 |
| rs557813544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232433 | ATAGAAGAAATTTCA[C/G]TGTTATTTCTTAGTA | 55120 |
| rs557912675 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239332 | AGAAGGACAAAACAA[A/T]CTTTCTGTAGTATCC | 55120 |
| rs557951612 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226096 | TCCTTTAAAATACTA[C/T]GGTGTCTTTCTTCTA | 55120 |
| rs557977028 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187059 | ACCCAGCAATCCCAT[G/T]ACTGGGTATATACCC | 55120 |
| rs558004494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226996 | TCAAATCTAATTTGC[C/T]GAGATATATTAAACT | 55120 |
| rs558048995 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58218440 | ACAAAAAACTCATGT[G/T]GAAAGAAAAAGGCAG | 55120 |
| rs558102386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58167880 | GACATCAAAACTATT[A/G]TATCAGTAAGCTATG | 55120 |
| rs558106588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238456 | ACCAACATAGAGAGC[A/G]TCATTACAGATCCTA | 55120 |
| rs558107836 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200652 | TACATACACAGCTCA[G/T]TATGCTAAAAGAGAG | 55120 |
| rs558134151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224542 | TAGAAGGTTCTTATT[A/T]GCATTAAAAAAGGAC | 55120 |
| rs558141101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231838 | TTTAAATATTTTTTT[A/T]AAAATGAGAGAACTA | 55120 |
| rs558178418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198494 | TGGATTTTGGTATTT[A/T]CAGAGGGCCCAAGAA | 55120 |
| rs558181379 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58189416 | AGTAACAATCCTCAC[-/A]AGTAAGGACAAAGAA | 55120 |
| rs558189058 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58225229 | TCATAAAGATACTTT[-/A]AAAAAAAAAACACTT | 55120 |
| rs558217328 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198880 | AAAAAATACAAAAAA[A/T]TAGCCAGGCATTGTG | 55120 |
| rs558257914 | snp | A/C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169735 | AAGCTGAAAAACACA[A/C/G]CACGAGAACTTTGTG | 55120 |
| rs558312702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211487 | GGAGACATTTTCCCC[A/T]TTATCTTGGGGACTA | 55120 |
| rs558326394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196331 | AGAAATATAGATGTA[A/T]CTGAACCAAAAGTGA | 55120 |
| rs558339546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175662 | AGCTATCTATGACAA[A/T]CCCACAGCCAATATC | 55120 |
| rs558347088 | in-del | -/TATGGGA | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58213954 | ATATCGGAGCTGCCC[-/TATGGGA]CAACTCTAGGGAGCA | 55120 |
| rs558363042 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58196945 | GAAAATGTGTATTTT[A/G]AAAAAAGGGACATGG | 55120 |
| rs558402979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205148 | TCAGAATATAAGCCT[C/T]CTAACTTAGGAAATA | 55120 |
| rs558407407 | in-del | -/A | 0.245631 | 0.249962 | intron-variant | FANCL | GRCh38.p7 | 2:58170694 | AAGCAAATGGAAAGC[-/A]AAAAAAAAAAAAAAG | 55120 |
| rs558471821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179955 | ACATTTATGCGGCCA[A/G]CAAACATATGAAAAA | 55120 |
| rs558508469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175314 | TCTGATACCAAAGCC[A/G]GGCAGAGACACAACC | 55120 |
| rs558525035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210902 | GGGGAGCTAGACCCC[A/T]GTGATTTTGCAGGGT | 55120 |
| rs558539189 | in-del | -/TC | | | intron-variant | FANCL | GRCh38.p7 | 2:58171098 | GCACCACATCACACT[-/TC]TTTTAAAACTGATCA | 55120 |
| rs558541743 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236360 | AGTGACAAAATTATA[C/T]AGTTGATAAACCAAT | 55120 |
| rs558611403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171073 | ATTAACAAAACATAC[A/G]TTCCTCTCAGCACCA | 55120 |
| rs558613519 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242102 | TTATTTGATTTTCCA[A/G]TTTTCCAATTTTCCA | 55120 |
| rs558625360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58184993 | TATTTGTTGGTATGC[C/T]TTAACGTGGGGTAGG | 55120 |
| rs558634553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58179539 | CTAGCCATATGCAGA[A/G]AACTCAAACGGGACC | 55120 |
| rs558664846 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215626 | GCCATTTTCCTCAAT[A/T]TATTTATCAATTCTG | 55120 |
| rs558685335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199175 | TGGAGGTGCAAGTTT[A/G]GTGATTTGGAAGTGC | 55120 |
| rs558701891 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213799 | TCTTTCACAAATCTA[C/T]GCAACAGATTTTGAA | 55120 |
| rs558746642 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58182391 | GCCATGCTTGTTTCA[C/G]TCCAAATATTACCAG | 55120 |
| rs558754886 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58166085 | AGTAGACTATACACC[C/T]GAGAAAGAATGGTTT | 55120 |
| rs558759579 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190242 | TAACTGATCACTGAT[C/G]ACCCATCATTTAAAA | 55120 |
| rs558774855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183561 | GTGGTTTTGTTCTCA[C/T]TCTGCTTCATTGATT | 55120 |
| rs558816519 | snp | A/T | 0.000676897 | 0.0183845 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159514 | TCAAGATCTCCATCT[A/T]GGTATAAATACACTT | 55120 |
| rs558871725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174497 | ACTCACTCAAAACCG[C/T]TCATCTACATGGAAA | 55120 |
| rs558922788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165660 | CAACTGTCATTGTTA[G/T]ATTTATTTTCATAAT | 55120 |
| rs558926664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210402 | CATTACCATGAGAAC[A/C]ATATGGGGGAAACCG | 55120 |
| rs558992194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163634 | ACCCACGGAAAGATT[A/C]ACCAAATGTTTTGTA | 55120 |
| rs559004460 | in-del | -/TCTC | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58191919 | GACACAGATATTCTT[-/TCTC]TCTTTTTATAAATAA | 55120 |
| rs559013560 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183497 | CAGCATTTTGTAGGT[C/T]CTATTGAATCTTTAT | 55120 |
| rs559028388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163291 | GCGCCATTACACTAC[A/C]TACTGGGCAACAAGA | 55120 |
| rs559060988 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163275 | GCGGTGAACCGAGAT[C/T]GCGCCATTACACTAC | 55120 |
| rs559080311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169013 | GGAAAGGGGCGGCTG[G/T]GGGCACAGCTTCAGC | 55120 |
| rs559112022 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185305 | TCTCTGCACCTAAAT[C/G]AGAAATACCCTGACT | 55120 |
| rs559141836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193995 | TAATGCTCCCTGCTA[C/T]GTAATAGGACTGACT | 55120 |
| rs559181672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239907 | AAAATATATACAAAA[C/T]ATTTTTAGACACGTA | 55120 |
| rs559198554 | snp | C/T | 1.87233e-05 | 0.00305962 | intron-variant | FANCL | GRCh38.p7 | 2:58222094 | CGCAAGACAATGAAC[C/T]GTTAATACCTGATTG | 55120 |
| rs559200572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229523 | TTTTTTCCCTATCAC[C/T]ACCATTCAGTCTCAG | 55120 |
| rs559242790 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58168458 | CACAACCCGCAGATC[A/T]GGAGATTCCCTCTGG | 55120 |
| rs559296990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194455 | AGAATAAAATTATGA[A/G]ATGTTCTCATCGTCT | 55120 |
| rs559333147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187631 | ACCTGATTTCTAGGC[A/T]GAAAAAGACAAGCAA | 55120 |
| rs559369376 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201617 | TTGATTGACCAAAGC[C/T]GAGGAAGCCCTGGGC | 55120 |
| rs559380132 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58185182 | AATAAAAAAAAAGAA[C/T]TAATCTTAAGGAAAA | 55120 |
| rs559412757 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58232590 | AAAATATATTTAGTT[A/C]CACAATCTATACAGA | 55120 |
| rs559439317 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214781 | GCCCCCCAAAGTACT[A/G]GGATTACAGGTGTGA | 55120 |
| rs559441062 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58240213 | AAGAAGAATACTTCT[A/C]ATTGGAGAGGGAAAG | 55120 |
| rs559449415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226574 | GCAGTTCAAGAAATG[C/T]GTCATCTATATTTAT | 55120 |
| rs559492975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212667 | TTTTTTTAATAGGCC[A/G]TTCTGTAAAACAACA | 55120 |
| rs559525907 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58233704 | GTCAGGAAAAAAAAT[A/G]CATGGGAGAGAGACT | 55120 |
| rs559531854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58176550 | TTCCCTATTTAATAA[A/G]TGGTGCTGGGAAAAC | 55120 |
| rs559566898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207685 | AAAAAATATCTTGGT[A/G]TTTGGTGTATGGAAG | 55120 |
| rs559582704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177075 | GCAAATCAAAACCAC[A/T]ACGAGATATCATCTC | 55120 |
| rs559618633 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58172944 | GAGAAGTGCTTAAAG[C/G]AGCTGATGGAGCTGA | 55120 |
| rs559640853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213410 | AGCCATAAAAATAAA[C/G]TTGATAGGTTTTGTC | 55120 |
| rs559668255 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58197109 | GGCTCTCTCTTCTCT[A/G]TTTTGCTATGTTTTC | 55120 |
| rs559691891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192319 | TTCTTTAATCTGGCA[A/C]GTAAGTGAGATTCAA | 55120 |
| rs559697248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212135 | AAAAGAAAGAGGTTT[A/G]ATTGGACTTACAGTT | 55120 |
| rs559701888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205250 | CAAGAAATGCACAAT[A/G]AAGTTGTGAAACACT | 55120 |
| rs559730339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58206970 | TTTAACTTACCTTCT[C/T]CAGTTTGGTAATAGG | 55120 |
| rs559802038 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58193031 | AATTTTAAAATACTT[A/C]AGAAAAAATTCAACA | 55120 |
| rs559810347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238585 | CTACCAAAGCTCACT[A/C]AAAAGGAAAGAGAAA | 55120 |
| rs559839501 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201867 | GTATTCCAGAATAAA[C/T]AGAACAAATGCATTT | 55120 |
| rs559943049 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58191323 | AAGGAGTCATTTGGA[A/G]ACTGATACTCACATG | 55120 |
| rs559971301 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58226576 | AGTTCAAGAAATGCG[C/T]CATCTATATTTATGT | 55120 |
| rs559974919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175438 | AACGTTATCCACCAT[A/G]ATCAAGTGGGCTTCA | 55120 |
| rs559988074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185139 | ATGGAATCTAATCTT[A/C]CTATGGTGAAAAATC | 55120 |
| rs560001414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161308 | CTGGATAGATTTTCT[C/G]CCTTGGATACTTCAG | 55120 |
| rs560003114 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169315 | ACCTGCAGCAGAGGG[G/T]TCTGTTAGACGGAAA | 55120 |
| rs560009587 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58221484 | GATGATTCTTACAAA[C/T]CCTAGTTGCTAAAAT | 55120 |
| rs560025919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58185641 | TCAAAGACCCCGATA[A/G]TTAAGCAGGGTAAGG | 55120 |
| rs560026196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186326 | TGGTATATTTGGACC[C/T]TTGTCCTACATATCT | 55120 |
| rs560082390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58167597 | CAACTGCAAATAAAA[C/T]CCTAATTGCATTTTG | 55120 |
| rs560113419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190331 | ACATAGTCACCTCAT[G/T]TGTAGCCATCACAGA | 55120 |
| rs560116451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197941 | TTTCTACAGAGTTCT[C/T]TGGAATTTAAATTTA | 55120 |
| rs560137188 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180859 | AATCAAAAAAGAAAT[C/T]GAAACTTTTCAGAAA | 55120 |
| rs560147347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167137 | GAATCACTTGAACCC[G/T]GGAGGCAGAGGTTGC | 55120 |
| rs560205327 | snp | C/G/T | 0.000115525 | 0.00759936 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165861 | AACTGACTATAAATG[C/G/T]TTATTAAGGAGCTCT | 55120 |
| rs560268684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170867 | AGAAGCAACCAGATT[A/C]ATAAAGCAAGTTCTC | 55120 |
| rs560275823 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214252 | TATTTTTGGCTTTCA[C/T]CTATTATCGAAGTTA | 55120 |
| rs560286692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58197106 | ACAGGCTCTCTCTTC[C/T]CTATTTTGCTATGTT | 55120 |
| rs560317714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160277 | AGTGCATTATGTTTT[A/T]ATTCCAGAAGACTTA | 55120 |
| rs560320280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171552 | AGGAGATAGAGACAC[A/G]AAAAACCCTTCAAAA | 55120 |
| rs560322111 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210313 | CCCATCTTACACGGA[G/T]GGCAGCAAAGACAGA | 55120 |
| rs560395411 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242700 | CCCACAACTGTCCAC[C/T]GTTCCTTCTAAAAAT | 55120 |
| rs560428305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224231 | TGATATCTATACTTT[C/T]ACTCTGGTTCCCTTA | 55120 |
| rs560430991 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58170495 | AACAAAATAACCAGC[C/T]AGCATCATAATGACA | 55120 |
| rs560452986 | snp | C/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160513 | TAAGTTCCTGGCATT[C/G]ATAGACTTTCCCTAA | 55120 |
| rs560457649 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207416 | AAATGTAAATGTCAA[C/T]AGCCACACATGGCTA | 55120 |
| rs560463812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230756 | ACCCCTGCTCAAAAT[A/G]TGCTTTCTCTCCCCT | 55120 |
| rs560516342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198845 | TCATCCTGGCTATAC[A/G]GTGAAACCTCGCCTC | 55120 |
| rs560579823 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174543 | CAGAATGACTACTGG[A/G]TACATAACAAAATGA | 55120 |
| rs560582499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236468 | AAGCAACTAGTTAAA[A/C]AAAAAACACACACAC | 55120 |
| rs560604367 | snp | A/G | 1.65754e-05 | 0.00287879 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159663 | ACCTGTCCTTTTGAT[A/G]TTAGTATTTCTTGCT | 55120 |
| rs560637552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174587 | GATGTTCTTTGAAAC[C/T]AACGAGAACAAAGAC | 55120 |
| rs560642671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58235779 | AGGTAAAGGAAAACA[C/T]GAGCGTACTAAATAG | 55120 |
| rs560646102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210470 | CAAGATGAGACTTGG[C/G]TAGGGACACAGAGTC | 55120 |
| rs560662384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216231 | GTAGACTGACCTCTA[C/T]GAAAACTACAACCCA | 55120 |
| rs560703025 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58178895 | AAGGTCTCAGGATAC[-/A]AAATCAATGTACAAA | 55120 |
| rs560721969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223184 | TCCGTACAGCTGAGA[A/G]TATCAATATGGATTT | 55120 |
| rs560794512 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168590 | GCGCCTGCAACACCA[A/G]CAAGACAAAACTATT | 55120 |
| rs560813813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228335 | TCAACAATGCATGAA[C/T]ACATATGATTCACAT | 55120 |
| rs560818312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174083 | ATTCAACAAGAGGAG[A/C]TAACTATCCTAAATA | 55120 |
| rs560869007 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58215583 | CTAAAGAAGAGGGAA[C/T]AGAAGTGAAGTAAGC | 55120 |
| rs560874682 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241457 | CGGGCGGAAATGAAG[A/G]TGAAGCGCAGGCCAG | 55120 |
| rs560896744 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190319 | GGACCAAATGAAACA[C/T]AGTCACCTCATGTGT | 55120 |
| rs560912087 | in-del | -/CA | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188397 | CCTTTGCAGCCTTTG[-/CA]CATACATTTTGGAAT | 55120 |
| rs560923095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208310 | TTGACAAAGCAAATA[C/T]AAAACTGAAGTATAA | 55120 |
| rs560923151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58214634 | CCCACCTCAGCCTCC[C/T]GAGAAGCTAGGTGCG | 55120 |
| rs560923595 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158851 | GCTTTCCAAGAGACA[G/T]AACACTATAGCTACC | 55120 |
| rs560952225 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195768 | ATAAGAAGGTCAGAC[C/G/T]AAGATGAGACTAAAG | 55120 |
| rs560959943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209075 | TCCCAACATTCATCT[C/T]CTCTAAGAACTCTCC | 55120 |
| rs560979836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178929 | CACAAGCATTCTTAT[A/G]CACCAATAACAGACA | 55120 |
| rs561027973 | snp | C/T | 0.00243585 | 0.0348136 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163470 | AGCACTCAGGAAGCA[C/T]AGTAGGATGCCTGGG | 55120 |
| rs561034612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163905 | CCTGAAAAAGTTTAC[A/C]TTTCATAGAACTATG | 55120 |
| rs561063627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228865 | AATAGATCTTAATAT[C/T]AGACTACATAAACCA | 55120 |
| rs561066251 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58186682 | ACTTACAGGTGTAGA[C/T]ATGTATGTATGCCTT | 55120 |
| rs561083954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214083 | CCTAAAATTTATCCT[A/G]AGAAATTAAATAAGA | 55120 |
| rs561101064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188448 | TTTTTTTGTTTTTTG[G/T]TTTTTTTTTGAGATA | 55120 |
| rs561150688 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58203887 | AGTCTATAAAATTGT[-/A]AACTGTAGTATTTGT | 55120 |
| rs561158668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169888 | GAACAAAGCCTCCAA[A/G]AAATATCAGACTATG | 55120 |
| rs561189122 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58217118 | ACACACACACATTAC[-/AT]ATATATATATATTTT | 55120 |
| rs561198934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202425 | CAAAGACAGCTATGG[C/T]GTATATATGAAAGCT | 55120 |
| rs561211331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187261 | TGAGTACATGTCCTT[C/T]GTTGGGACACGGATG | 55120 |
| rs561221909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169503 | CACCTTTTCTCCAAC[A/G]GATCACAACTCCTCG | 55120 |
| rs561226984 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240747 | GGTGTACAGGTACAT[A/T]CGACTTGGCAAAGGG | 55120 |
| rs561236519 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58185511 | TCACCAAATCACGAA[A/C]TTACAAAAAAACTAA | 55120 |
| rs561246298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187542 | GCACGTTGTGCACAC[A/G]TACCCTAAAACTTAA | 55120 |
| rs561275468 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58218001 | ATAATTAAAAGGATG[A/G]TTTCTGACAAAAGTA | 55120 |
| rs561287912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58220452 | TAAAAGCCTTTTAAG[A/G]AATATAAAGGGAAGT | 55120 |
| rs561364130 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | FANCL | GRCh38.p7 | 2:58177204 | TAAACTAGTTCAACC[A/C]TTGTGGAAGTCAGTG | 55120 |
| rs561414110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177687 | CTTAATGCTAAATGA[C/T]GAGTTAACGGGTGCA | 55120 |
| rs561449827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227339 | ACAAAGAACTTTCTG[C/T]ATCCCGTGGTTCCTG | 55120 |
| rs561473848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168960 | AAAGTCAGAGGCTTA[C/T]AGATAAAACTCCCAT | 55120 |
| rs561498372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172561 | TTAACAGAGGGTCTG[C/T]TTGTTAACAGAAAGG | 55120 |
| rs561552139 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58185446 | AACTAGCATATCTGA[C/T]ATTTAAACCTTGAGA | 55120 |
| rs561590124 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212071 | AATTTACTGTATTAG[C/T]CTGTTTTCATGCTGC | 55120 |
| rs561597573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234416 | GGAAGAACAAAATGA[A/C]ATACAAATGTCATAA | 55120 |
| rs561600384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162576 | TGTGAAATCTCTGTA[C/T]ACAGAGGGCCGACTT | 55120 |
| rs561624122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239864 | GAATTACTTGTACTG[C/T]ATATCCTTGCTACTT | 55120 |
| rs561665886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172252 | GAAGAGAGCAGTGGT[G/T]CTCTCAGCACGCACC | 55120 |
| rs561676982 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168691 | CCCAGCAAGCTAAGA[A/T]CCACTGGCTTGAAAT | 55120 |
| rs561684406 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58224987 | CAAATACTATTTCCC[A/G]CAAAGAAATCATGAT | 55120 |
| rs561698548 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58216858 | CAAGCACGGGGGTAA[A/C]GCGGGTGAGGAGAAG | 55120 |
| rs561746383 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58206880 | GTCACTTTGTTTGGG[G/T]CACAGAAAGAAACCT | 55120 |
| rs561759044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163250 | GTCATTTAAAATAAC[C/T]ATCATTATTGCGGTG | 55120 |
| rs561815644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58175859 | TCCCTGTTTGCAGAC[A/G]ACATGATTGTATATC | 55120 |
| rs561833481 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58193342 | AAGCATTAATGGTAA[C/T]TTTACATTTTAATTT | 55120 |
| rs561851791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212525 | AAGCATAAATTAGGG[C/G]TGTCCTAGGCAAAAT | 55120 |
| rs561860658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191423 | CATTAAGTTCATCAA[A/G]GTACTCACAATATAT | 55120 |
| rs561898634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225873 | ATACATAAGTACCTT[A/G]TAAGTCTTATATAAG | 55120 |
| rs561901520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238148 | AAACTTTCTTAAAAC[A/G]TTATGGGATTTTTTG | 55120 |
| rs561994165 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196369 | TTAACATTTGTCAAA[A/T]CTGAGTTGTGATAAA | 55120 |
| rs561994261 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172148 | AGGCCTGCCTGCCTC[C/T]GTAGGCTCCACCTCT | 55120 |
| rs562000847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212203 | GCAAAGAGGAGCAAG[C/T]CCCATCTTACATGGA | 55120 |
| rs562011152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58219574 | ATACTACCTCACCAG[A/G]TAATCAAGATCAAGA | 55120 |
| rs562055423 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58173670 | ACAACCGGTACCAGC[C/T]GCTGCAAAATCATGC | 55120 |
| rs562064230 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58219003 | CAATAGCAACAAGCA[-/C]CCCATAGTGCCCACA | 55120 |
| rs562065162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218856 | AGTTGTAGACATCAG[C/T]ATAAAATCATGTTTA | 55120 |
| rs562126730 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198081 | TGCATGGGTGTGGGT[A/G]TGAGTGGGTGTGTTT | 55120 |
| rs562128079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185902 | AATTACTTGTACACT[C/T]AGGTCTAAACATTTT | 55120 |
| rs562131075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211247 | ACTTCTGTGCACCCA[A/C]AGGCTCAACAACATG | 55120 |
| rs562132646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197727 | CTAAAGCACAAAATA[A/G]AAGAATATAATCAAA | 55120 |
| rs562168201 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58211586 | TTTCTTTTCTATCAC[A/G]TTGTCAGGCTGCAAA | 55120 |
| rs562221812 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182476 | TCATAACTTTGACTT[G/T]CGTTGTTAATGTTTA | 55120 |
| rs562270185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166998 | GTGCGCAGATCACGA[A/G]GTCAAGAGATAGAGA | 55120 |
| rs562291272 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234547 | TACATATAATTGGAG[A/T]TCTTGGAAAGAAAAA | 55120 |
| rs562291641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217382 | CTAGGAGAGAATCTA[C/T]TCCTTGCCTCTTCCA | 55120 |
| rs562294011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191720 | ATAAATCCACAAATA[C/T]ACAATATCATTACAC | 55120 |
| rs562296631 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58204510 | GTTTTCCATCACTGG[A/C]ACCTTTGGCACACAC | 55120 |
| rs562307386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161798 | AACATTTACCTTTTA[C/T]GTTGGGAACATTACA | 55120 |
| rs562334040 | snp | A/G | 1.77697e-05 | 0.0029807 | intron-variant | FANCL | GRCh38.p7 | 2:58198541 | TACTCTGGGACAACT[A/G]TACTTTTTAATTACT | 55120 |
| rs562382460 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162014 | ATATACACAGCTAGG[C/T]TAAAAAAAGAGATTC | 55120 |
| rs562420293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179550 | CAGAAAACTCAAACG[C/G]GACCCCTCCCTTACA | 55120 |
| rs562443957 | in-del | -/CTAT | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163864 | ATGTTTAAGAAATAA[-/CTAT]CTAAATTATTTTTCA | 55120 |
| rs562456459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231214 | CTTTCTCTTCTACCC[C/T]GCTAGACACAGCACC | 55120 |
| rs562512390 | in-del | -/AAGA | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58237507 | TCTGTACTAGAATAG[-/AAGA]AAGATCTCATATCAA | 55120 |
| rs562516436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230662 | TCACAACTCTCTCCA[C/T]TCTTGGTCTTCAAAT | 55120 |
| rs562517140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204645 | TGTTTTTCTCCTCAA[G/T]GAACTTCTCCTATAT | 55120 |
| rs562522528 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219919 | GGAAGACATCCAAAC[A/G]TAAAATCCCTACTGC | 55120 |
| rs562551159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224127 | TTTAGTTTTAAACTA[A/G]TAAGTGTTTCTCCAA | 55120 |
| rs562572558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196434 | TTTCAGTATATTCCA[C/T]AAATTAAGAATTTAT | 55120 |
| rs562583530 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58175087 | AGACTAAACCAGGAA[A/G]AAGTTGAATCTCTGA | 55120 |
| rs562616425 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207646 | TATAACTAATAGAGA[C/T]TATTTGTATCAATTT | 55120 |
| rs562666261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170830 | GAGAGCTAACAATCC[C/T]AAATGTATATGCACC | 55120 |
| rs562695267 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58174059 | CATTACATAATGGTA[A/C]AGGGATCAATTCAAC | 55120 |
| rs562730257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203806 | TACAACTTGGGATAG[C/T]GGAAGTGTCCACTGT | 55120 |
| rs562768101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236445 | AATATGTATATTATA[A/T]ACCCTTTAAGCAACT | 55120 |
| rs562772305 | snp | A/C | 1.65141e-05 | 0.00287346 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159558 | GGGGATCACAGACTT[A/C]GAAAGTTCAACTGGA | 55120 |
| rs562804913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237053 | TAACTGATAGAAAAA[C/G]CAGACAAAAAAGTCA | 55120 |
| rs562819076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178251 | AGGCCTGCATCATCC[C/T]GACACCAAAATCTGG | 55120 |
| rs562836161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229980 | AGAATGACAAACATA[A/T]TTTGGACAAGTTAAT | 55120 |
| rs562858175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173699 | GCCAAATTGTAAAGA[C/T]CATCGAGGCTAGGAA | 55120 |
| rs562878747 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210711 | AGGGGTATAGGCATT[C/G]GATAAATACAGCCAT | 55120 |
| rs562886511 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240653 | TGTGTAATAAACTCC[A/T]TATGAGAGGCCACTG | 55120 |
| rs562908124 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159085 | TATTTATTTTTAGAT[C/T]ATAAATTACTTAAGA | 55120 |
| rs562987865 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241595 | CAATTGTCCCAGGAG[C/T]CCTTTCGATGATTCT | 55120 |
| rs562989417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58170387 | AGCTCCTGAAGGACG[C/T]GTGAAATATGCAAAG | 55120 |
| rs562993644 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58174166 | CCTACAAAGAGACTT[-/A]AGACTCCCACACAAT | 55120 |
| rs563020028 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58183673 | CTCTTCTTTGTACCT[C/T]TCCATATTTTCTATA | 55120 |
| rs563025138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165164 | TTATAGTCGAGAACA[C/T]GATAACATTGCACAG | 55120 |
| rs563028488 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229170 | ACAGAAATATAGAAA[A/G]TCAGGAAAAAAACAC | 55120 |
| rs563039004 | snp | A/G | 0.000198863 | 0.00996956 | synonymous-codon, missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241221 | CTGGGCGGGTACCTG[A/G]GCCGAGATGAATCCC | 55120 |
| rs563059398 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58215396 | CAATATCATAATATA[C/G]TACACTTACAATTAT | 55120 |
| rs563149618 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58228778 | CCTAACCAATTGGGG[A/G]GCAAGGAAAGATAAA | 55120 |
| rs563260350 | in-del | -/GACA | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58171866 | GTCAAAGAAAGGGGT[-/GACA]GACAGCACCCGGAAA | 55120 |
| rs563269012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228223 | GAAATAATCTCTAAA[C/G]TACAATAAATATTTA | 55120 |
| rs563274180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227885 | ACAACCTCATCATTA[C/T]TTTTTTTAAAGAAGA | 55120 |
| rs563284619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58221669 | AAATTTAGAATACAG[C/T]TGTATGTTCAGTGAA | 55120 |
| rs563290732 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226478 | CATTTTATTTCTTCA[C/T]CACCTGCCCAACACT | 55120 |
| rs563337261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183112 | GCCTAATGAAACAAT[A/G]GCAAAATATCTGTAC | 55120 |
| rs563341572 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58195023 | AGGGATTTTTAAAAA[A/C]TCAATTATCTGAAAT | 55120 |
| rs563378210 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164201 | GAAATTTTACTTCTA[-/T]TTTTTTGAAGGTACA | 55120 |
| rs563400546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188365 | TCTTTTTCAGAGTTA[C/T]TTTAACTATCACAGG | 55120 |
| rs563429304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58235287 | ACCCAAAGGTGGGAA[C/T]GTACAGGAACAGTCT | 55120 |
| rs563503720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194496 | CTATAAAAGATTAAC[C/T]GAGCAAACAAATAAA | 55120 |
| rs563505648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202338 | ATGCTGAACTTGTTT[A/G]TTCTACTTATTTGTC | 55120 |
| rs563513081 | snp | C/G | 0.000315068 | 0.0125473 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226763 | TCATAAAGCTCATTA[C/G]ATCAGGAGAGTGCTG | 55120 |
| rs563516921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213465 | ACACAAACAGAATTA[C/T]CTTCTTTGGCTTCTC | 55120 |
| rs563536951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163713 | ATGATTATCATTGAA[A/C]GGATCTTAAATTTCA | 55120 |
| rs563547898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227280 | AGCCATCCATAGGCA[C/G]CTTGTGTTAGTCAGC | 55120 |
| rs563550275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219797 | GTTCACATTATTCAT[G/T]AAGTGGCAGGTTGGA | 55120 |
| rs563553886 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58207781 | AGTCTGTTTCATGTC[A/G]GGCATAATGACTCAT | 55120 |
| rs563561001 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58173248 | ACTTCCCCAATCTAG[A/C]AAGGCAGGCCAACAT | 55120 |
| rs563603934 | snp | A/G | | | | | GRCh38.p7 | 2:58243396 | TTATAGCAGAATACC[A/G]TAAACTGGATAGGTA | 55120 |
| rs563623426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169484 | AAAATTCCAAAAACC[A/G]GAACACCTTTTCTCC | 55120 |
| rs563644058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58193852 | TTCACCATTTCCATA[C/T]ACAGTACATACGAAC | 55120 |
| rs563661204 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235021 | TGTCTGGTTCTATGA[C/T]GGGAGTATTTTCAGG | 55120 |
| rs563721327 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58177542 | AAGAACAAAAAACCA[A/G]ACACCGCATATTCTC | 55120 |
| rs563721387 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173011 | GCCTCAGGAGCCGAT[G/T]CGATCAACTGGAAGA | 55120 |
| rs563722600 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58213966 | CCCTATGGGACAACT[C/G]TAGGGAGCATCATTC | 55120 |
| rs563767036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192417 | ATGGAGGTTGAATGA[C/G]TTATAACAACTTAGA | 55120 |
| rs563768937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58199149 | TGAAGAGCTTATTTA[C/T]AGTCAACCTATGGAG | 55120 |
| rs563769867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181165 | GATGTTTGTCAACAG[A/G]CAAAAGGATTAACAA | 55120 |
| rs563783128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177140 | GAAACAACAGGTGCT[A/G]GAGAGGATGTGGAGA | 55120 |
| rs563830352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186845 | GAGTAAAAAGTGCTG[A/C]AAAAATCAAAACCAG | 55120 |
| rs563927719 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58173047 | TATCAGTGACGGAAG[A/G]TGAAGTGAATGAAAT | 55120 |
| rs563940973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187158 | TAGCAAAGACTTGGA[A/G]CCAACCCAAATGTCC | 55120 |
| rs563988349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175821 | TAAAGGGTATTCAAT[C/T]AGGAAAAGAGGAAGT | 55120 |
| rs563988575 | snp | C/G | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188595 | CAGACACGTTGCCCC[C/G]ACACCCAGCTGATTT | 55120 |
| rs564011391 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172172 | CACCTCTGGGGACAC[A/G/T]GCACAGACAAACAAA | 55120 |
| rs564049364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175483 | GGCTGGTTCAATATA[C/T]GCAAATCAATAAATG | 55120 |
| rs564051210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180477 | AAACCAAACACTGCA[C/T]GTTCTCACTCATAAG | 55120 |
| rs564069416 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58168223 | AAGGCAGAAGGCAGG[G/T]GATTTCTGCATTTCC | 55120 |
| rs564081004 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201436 | GTATTTTTTAGACTC[C/T]ATAATATTAATATAT | 55120 |
| rs564145215 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212169 | CATGGCTGGGGAAGC[A/C]TCACAATCATGGTGG | 55120 |
| rs564220265 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58174108 | TAAATATATATGCAC[C/T]CAATACAGGAGCACC | 55120 |
| rs564244156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160354 | TAGCAGACTATTAAG[A/C]TGTTGAGTAACAAGG | 55120 |
| rs564289517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211720 | CCAGATACCCTAAAT[C/T]ATCTCTCTCAAGTTC | 55120 |
| rs564292390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231312 | CCAGGTCTCACACTC[C/T]ATTTCCACACCACTA | 55120 |
| rs564318944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58191632 | CACGTAAATAAAATG[C/T]TGTCTTTAAAGTCTT | 55120 |
| rs564321704 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206971 | TTAACTTACCTTCTC[C/T]AGTTTGGTAATAGGA | 55120 |
| rs564354252 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237629 | TAAAGACAGGTTCTT[C/T]GAAGAAATCAGTAAA | 55120 |
| rs564380752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176136 | AATAAAAGAGGATAC[A/T]AACAAATGGAAGAAC | 55120 |
| rs564385897 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180616 | AATGTAGATGTCGGG[G/T]TGATGGGTGCAGCAA | 55120 |
| rs564462340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58165955 | TAAAATACACTCAAT[C/T]TAGAAATTTTAAGCT | 55120 |
| rs564478686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224732 | AGCATAAGTGAAATA[C/T]AACAAGTAGAACATA | 55120 |
| rs564482115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166377 | ATTAGGCAGAGTATG[A/T]AAAGGTTTTACACAT | 55120 |
| rs564529345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197650 | ATCATCAATGTACTG[C/T]GAAATTCAACTGACA | 55120 |
| rs564542627 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58202927 | ACGGCTAATTTTACT[A/C]AGGTACAAAATATAA | 55120 |
| rs564562510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191097 | ACAAGCATATAAACA[A/C]CCACATATTCCAAAT | 55120 |
| rs564581763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211180 | CTGGGCATCCAGGAA[G/T]TTCCATACATCTTCT | 55120 |
| rs564603582 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58237328 | CAAAAAGATATCTAG[A/C]AAATCCTTAATATTG | 55120 |
| rs564606654 | snp | A/G | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164445 | AACACATTATTTACT[A/G]TGAACAGAAATTTCT | 55120 |
| rs564635872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230942 | CACCTCTTTTTCTTC[A/C]AAATACTTTATACTT | 55120 |
| rs564648345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171326 | TTTTTGAAACTTAAG[C/T]TATTGAGAACAAAGA | 55120 |
| rs564684477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223286 | TAAAAATAGACTGAT[A/G]GTCCACCAAAATAAA | 55120 |
| rs564709100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229075 | ATAGTTTATCTCCTA[C/T]ACTTCTTTGCAGCTT | 55120 |
| rs564726028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58203960 | ATAAAACTGTCTAGG[C/T]TTTTGGAAACGTGGT | 55120 |
| rs564747338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58222350 | AAATTCATCCTCAAG[A/G]CTTCACTATGGCTCT | 55120 |
| rs564747999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217348 | AGGTGTCAGCAAAGA[A/T]GTGCTCCCTCTGGAG | 55120 |
| rs564751748 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222544 | TTTTTCACTGACTTA[C/T]ACTCTGTACTATTCT | 55120 |
| rs564753728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185925 | AACATTTTAAAAAAC[A/G]TATTAGTACCTATCA | 55120 |
| rs564756554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175030 | AATAAACTAGAAAAT[C/G]TAGAAGAAATGGATA | 55120 |
| rs564772448 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182819 | ACTAGATACTGGTGA[C/T]ACTAACAATATAGAA | 55120 |
| rs564782107 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58166233 | AACATTGGACCTATA[A/C]AAAATGTCTATAATA | 55120 |
| rs564915036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58210647 | CAAGTCTCTTCCACC[A/G]ATGAGCCTAATAAAA | 55120 |
| rs564948240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58178949 | AATAACAGACAAACA[A/G]AGAGACAAATTATGA | 55120 |
| rs564958425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58203215 | GAGAGAATTAGTCAT[C/T]TCTCAACCTGTCTGT | 55120 |
| rs564999425 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185049 | GCCAAACAAGAGAAA[C/G]TAGAAAACTACCTCT | 55120 |
| rs565052298 | in-del | -/A | 0.415727 | 0.187175 | intron-variant | FANCL | GRCh38.p7 | 2:58202239 | CTATACCTTTTTCCT[-/A]AAAAAAAAAAAAAAA | 55120 |
| rs565055427 | in-del | -/TCTT | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58193377 | TGCTTGTATTTTTCC[-/TCTT]TCTCTTCTTTTTTAG | 55120 |
| rs565080914 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58209129 | CTTCAAATTCCTCCA[A/C]ACTCACATTGCTCCT | 55120 |
| rs565084625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189078 | AAAGCACATCAGTAG[C/T]TGCCTGAGGCCCTGG | 55120 |
| rs565114856 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58209745 | AAGAGATTAAGTTTG[A/C]CCAAGATCACACAGC | 55120 |
| rs565143090 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158978 | AATCACATTAATGAC[C/G]AAAATATTTCTAATT | 55120 |
| rs565173334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164970 | CTCACTAACTTGGAT[C/G]TGATTCACATCAGAA | 55120 |
| rs565182708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178227 | GACTCCTCCCTAACT[A/C]ATTTTATGAGGCCTG | 55120 |
| rs565220485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235998 | TGACAACTTAAAGTG[A/T]CCTAAATGCATGTAT | 55120 |
| rs565224889 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215229 | CAGGAACTGCTGCTA[C/G]GGCATCTCAACTTTT | 55120 |
| rs565238061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164489 | CACTGTCATCTGGTA[A/G]TGGCTCCAGACAGTA | 55120 |
| rs565243859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177746 | TGTAAGTAACCTGCA[C/T]ATTGTGCACATGTAC | 55120 |
| rs565249638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183071 | TTATTATAAGACATA[C/T]AGTACTCATCCTAGA | 55120 |
| rs565256161 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58217781 | CTCCAGAGCTCTCAG[A/G]ACAAGCGGACAAAAA | 55120 |
| rs565362537 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58173672 | AACCGGTACCAGCCG[A/C]TGCAAAATCATGCCA | 55120 |
| rs565374294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181923 | ATATTTAATAACTGG[C/T]CTTTTAAAATAAATC | 55120 |
| rs565403012 | in-del | -/T | 0.00348583 | 0.0416024 | intron-variant | FANCL | GRCh38.p7 | 2:58228072 | TTAACAATATGGTCA[-/T]TTTTTTTATTTTTCC | 55120 |
| rs565429652 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | FANCL | GRCh38.p7 | 2:58190585 | GGTGCTACCATCCAT[A/C]AAGAAAAAAGTTAGC | 55120 |
| rs565443939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221492 | TTACAAACCCTAGTT[C/G]CTAAAATTTACCACT | 55120 |
| rs565469067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221017 | GGAGATCGAGACCGA[C/T]CCTGGCTAACACGGT | 55120 |
| rs565480207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214714 | ACGGGGTTTCACCAT[A/G]TTGCCCAGGTTGGTC | 55120 |
| rs565483115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183624 | GTGGTTATATTTTAA[A/T]AATCCTCTTTTATGA | 55120 |
| rs565562530 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58234425 | AAATGAAATACAAAT[C/G]TCATAAAGGGCAAAG | 55120 |
| rs565577240 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | FANCL | GRCh38.p7 | 2:58176849 | TGAACAGGCAACCTA[C/G]AAAATGGGAGAACAT | 55120 |
| rs565580579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162654 | TGGATTTTTGTATCC[A/G]TGGGCAGCCCTGAAA | 55120 |
| rs565597906 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231479 | TTCCTTTTTCCCTCT[C/T]AACTACACTTCTGTT | 55120 |
| rs565605898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228150 | CTAATCCATATTAGT[C/T]AAAATGGAGACAGTC | 55120 |
| rs565650980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227441 | TAGCTCTCAGTAGAT[A/G]TGGGAGACAGAAGGG | 55120 |
| rs565678875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220669 | AAGATATGTTCCTTG[C/T]TCTCTTTTAAATGGC | 55120 |
| rs565679072 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162225 | CCTTGTCAAAAATCA[A/G]TTCTATTATTTTTGC | 55120 |
| rs565694717 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212556 | GGTATGCATGATAAG[C/G]TACTCAAAGCAAAAG | 55120 |
| rs565715795 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58171443 | GAACTAAAATTGACA[A/C]CCTAACATCACAATT | 55120 |
| rs565726138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186950 | GGAGAAATAGGAATG[C/T]TTTTACACTGTTGGT | 55120 |
| rs565782861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167369 | AAATTAAACTCCCAA[A/G]AAGCTAGTTTTAAAA | 55120 |
| rs565816150 | in-del | -/AT | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241999 | CTGACAGCGCTTGCA[-/AT]ATGTTTTTCTAACTC | 55120 |
| rs565820667 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58172512 | GGAGTGGACCTCTAG[A/C]AAACTCCAACAGACC | 55120 |
| rs565827390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239346 | ATCTTTCTGTAGTAT[A/C]CCTGCCAAAAATGCA | 55120 |
| rs565827393 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192061 | AGCCTACTGTGAAGG[A/T]CTATAGTAAAGTCAT | 55120 |
| rs565836641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232386 | AGTCACTCACAAACA[C/G]AAGAAATATTACAAA | 55120 |
| rs565858375 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193900 | ATGTGACTTGTCTGA[A/G]TAATACAATTAAATT | 55120 |
| rs565858589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238895 | AGAGGAAATGCAAAG[C/G]CTTAAAAACTTACAT | 55120 |
| rs566009679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175629 | AGGTATTGATGGGAC[A/G]TATCTCAAAATAATA | 55120 |
| rs566031779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212225 | TTACATGGATGGCAG[C/G]AGGCAAAGAGAGAAT | 55120 |
| rs566047622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231441 | TTAGAGATCTGAGCC[A/G]GGAATTTGAAAAGCA | 55120 |
| rs566048942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171978 | GGAGAGTCCTACGCC[A/C]ACGGAGCCTCCTTCA | 55120 |
| rs566090549 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58237615 | AAAATTGAAGAAATT[A/C]AAGACAGGTTCTTTG | 55120 |
| rs566144356 | in-del | -/ATA | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58196554 | ATTAATATTATTAAT[-/ATA]ATATTTATTCCATGC | 55120 |
| rs566170805 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58176130 | CAAGGAAATAAAAGA[C/G]GATACAAACAAATGG | 55120 |
| rs566188319 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167188 | CTGCACTCCAGCCTG[G/T]TGACAGAGCTAGACT | 55120 |
| rs566221051 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58192137 | CATTTGATTAAAAAA[A/C]CCTGTTCCATGCAAC | 55120 |
| rs566258722 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58191503 | TCTCTGTTATTTATA[A/G]TACAATGTATATGTA | 55120 |
| rs566276511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204716 | TTCATATACTCAAAT[A/T]GATCCTCTAAGGAAA | 55120 |
| rs566303498 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58187739 | AGCTTTAATGGTAGT[-/AA]AAGTGTTATCCTTGA | 55120 |
| rs566307697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180320 | GACTTGAAACCAACC[C/G]AAACGCCCATCAATG | 55120 |
| rs566327109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197301 | TTATATATTTACTTT[A/G]CTCATGTATTTATGT | 55120 |
| rs566364331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191368 | GGACACCTGCTATAT[A/G]AGAATATTTTACTGA | 55120 |
| rs566396082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224529 | CAAAGTCCTACCTTA[C/G]AAGGTTCTTATTAGC | 55120 |
| rs566509566 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58203543 | TTAGAACTAAAAAAT[A/T]AAGATGAAACAACCA | 55120 |
| rs566547511 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179886 | ATTTACAAGAAAAAA[A/C]CAACCGTATCTAAAA | 55120 |
| rs566554996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58171533 | AAGATCAGAGCAGAA[C/G]TGAAGGAGATAGAGA | 55120 |
| rs566555031 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58166065 | CAGGATTCTTTTTTA[C/T]TGACAGTAGACTATA | 55120 |
| rs566591193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166692 | AAATGTAAAGTCACA[A/T]ACTACAAACGTTTTC | 55120 |
| rs566606399 | snp | A/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242220 | TTTATTGACCTCAAG[A/T]CAGAATTTGACATCC | 55120 |
| rs566609377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196768 | TTATCTACATCTAAA[A/G]CACAAAGAAACTCAT | 55120 |
| rs566625366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179325 | ATCATGCTACCTGAC[A/T]TCAAACTATACTGCA | 55120 |
| rs566647339 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58223536 | CTATTCTGAGTCAGG[A/T]AAGTTACTCCTACTG | 55120 |
| rs566663530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174790 | AAATAACTAAAACCA[C/G]AGCAGAACTGAAGGA | 55120 |
| rs566681600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216739 | ACACTGTCCACCTTC[A/C]CATTCACACACAGGT | 55120 |
| rs566734132 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208611 | TGCATTTAAGTAGTA[G/T]TAACATCAACAGGCA | 55120 |
| rs566747454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188765 | CAATTTCTTAAATTA[A/G]GAAGGAAAAAAAAAA | 55120 |
| rs566805001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170136 | AAGGGCAGCCAGAGA[C/G]AAAGGTTGGGTTACC | 55120 |
| rs566812296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222751 | TGAAGTTACCAACCT[A/G]GATAGACAGCTTATT | 55120 |
| rs566821638 | in-del | -/GTGTGTGTGTGC | | | intron-variant | FANCL | GRCh38.p7 | 2:58198035 | GGCTGGATGGTGTGT[-/GTGTGTGTGTGC]GTGTGTGTGTGTGTA | 55120 |
| rs566842126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58164708 | CTTTAATGGGGCCAC[A/G]AAAATAATGATTTAC | 55120 |
| rs566858448 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223305 | CACCAAAATAAATTC[A/G]TATTTAGGTTGTGCA | 55120 |
| rs566890647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179037 | CAAGGGATGTGAAGG[A/G]CCTCTTGAAGGAGAA | 55120 |
| rs566914449 | snp | G/T | 1.72193e-05 | 0.00293417 | intron-variant | FANCL | GRCh38.p7 | 2:58232153 | CTCAAATTTTTATCT[G/T]TCACTTAATGCTGAG | 55120 |
| rs566936529 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58203409 | ACTCCAAGAATAATT[A/T]AAAAAAAAAAGTTGG | 55120 |
| rs566948289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236161 | CTTACGGAGGAAAAA[C/T]ATGAAAAAAGCTACA | 55120 |
| rs566973977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196178 | GCAAAAAGTATGCAC[A/G]GATGGCCTATATACC | 55120 |
| rs566993767 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241757 | AATGTATTATTTTGT[A/G]TATAATTATTGTAAT | 55120 |
| rs567111181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235574 | ACTTAGAGAACAAAA[A/C]TATCTAGCATGCAAC | 55120 |
| rs567192934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173833 | TCCAATTAAAAGACA[C/T]AGACTGGCTAATTGG | 55120 |
| rs567197918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240799 | AAATGTTCTTTCTAC[A/G]GGAAACACGAAAATA | 55120 |
| rs567200783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202865 | AGAGCTTGTAAAAAT[A/G]AGGACAGGGTGTATT | 55120 |
| rs567209195 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218744 | AATTAAGTAAATGGA[G/T]AACAGATAATGGGAG | 55120 |
| rs567213941 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186814 | CCACCACGAAGCTGA[C/T]TGAAGCAATGTGGTT | 55120 |
| rs567235212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214843 | GTCTTGCCTTATGTA[G/T]CCTTAGTGCTTTACA | 55120 |
| rs567248753 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58213238 | TCATTTCAAAAGATA[A/C]TTTAAATTAAGAATT | 55120 |
| rs567258574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178385 | AAGCTTATCTACCAC[C/G]ATCAAGTTGGTTTCA | 55120 |
| rs567274433 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220662 | TGCACTTAAGATATG[A/T]TCCTTGTTCTCTTTT | 55120 |
| rs567362847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173472 | CCAGAAGAGAGTGGG[A/G]GCCAATATTCAACAT | 55120 |
| rs567398162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58214408 | CTCTCAAGAATCCTA[C/T]AATTATACTCTACCC | 55120 |
| rs567409483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194595 | TCATGGCAGCAATAG[C/T]AGCAGCAGCCTTGCC | 55120 |
| rs567463627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182096 | AAATAGGCTGAAAAA[A/C]TACATCTTAACTTCT | 55120 |
| rs567466016 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187819 | ATTATTGAACTTTGA[A/G]AGTTCTTTATATATT | 55120 |
| rs567466969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227538 | CTCCACGTCATTCTG[A/C]CGGTCAATGGCCTGC | 55120 |
| rs567485643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213002 | TAATGTCTAATCCTA[C/T]AGAGTTGATTAGAAA | 55120 |
| rs567504675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58182679 | CACTGAAGAATGCAA[C/T]CCTCACTTACATCAC | 55120 |
| rs567527371 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187405 | GAACATCACACACTG[C/G]GGCCTGTCGTGGGGT | 55120 |
| rs567530643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207261 | AGGACAGGAACAACA[A/C]TCTATAAAGCAGTAA | 55120 |
| rs567628988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228511 | ACTGTTTTTGTAAAC[A/G]AAGTTTTATTGGCAT | 55120 |
| rs567636275 | snp | A/G | 1.66699e-05 | 0.00288698 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162839 | ATGCAATACTGTCTG[A/G]AATATCAAAACACTG | 55120 |
| rs567708975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186443 | AAATTTATTGGAAGT[C/G]AACTCAGGGAACGAA | 55120 |
| rs567742411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168536 | CATTTGGGCAGACAT[G/T]GAGCTAGCTACAGGA | 55120 |
| rs567744300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173039 | AGAAAGGGTATCAGT[A/G]ACGGAAGATGAAGTG | 55120 |
| rs567775076 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230415 | TCAAGAAACCCTCCC[A/G]CCTCAGCCTCTCAAG | 55120 |
| rs567776752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192558 | ACCACATTACTTATA[C/T]CTACATAGGATACAA | 55120 |
| rs567821086 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208925 | ACCCCTCTGTTTAGC[C/G]CTAATATGTTAATCC | 55120 |
| rs567830636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176243 | CCATCCCCATCAAGC[C/T]ACCAGTGACTTTCTT | 55120 |
| rs567902200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172778 | AGCAATGGAACAAAG[A/C]TGGACAGAGAATGAC | 55120 |
| rs567937474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58192091 | TATTTATTAACATCA[A/G]CAAGTAAATCAGTTA | 55120 |
| rs567937973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226896 | AGATTAGCTATATCT[A/G]CATCTGAAAACTATA | 55120 |
| rs567983578 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183208 | ATGAACAGATAATAG[A/G]AAAAAATGAATAAAG | 55120 |
| rs567992348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180676 | CAAACCTGCACGTTC[G/T]GCACATGTATACCAG | 55120 |
| rs568053733 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242122 | CCAATTTTCCAATGC[A/G]TCACGTTTGAGCCCT | 55120 |
| rs568065161 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189257 | ATTCAGTTTACTGTA[A/T]GTCAATTATATCTCA | 55120 |
| rs568129860 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239340 | AAACAATCTTTCTGT[-/A]AGTATCCCTGCCAAA | 55120 |
| rs568136722 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222574 | TTCAAGCAGGTAAGT[C/T]GGAGTATTATGCCAT | 55120 |
| rs568137431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238794 | ACCTATTAAGGTGCA[C/T]AGTAAATTGACATCA | 55120 |
| rs568148204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198259 | GTAAAAACAGTTACA[C/G]TTGGCCCTACCCACG | 55120 |
| rs568151673 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58194258 | TTTTCACATCCATTT[C/T]TGCTTGATCAGTGAC | 55120 |
| rs568156956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171638 | GAGCCAAGATGGCCG[A/C]ATAGGAACAGCTCCG | 55120 |
| rs568191767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232385 | AAGTCACTCACAAAC[A/C]CAAGAAATATTACAA | 55120 |
| rs568214467 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58197255 | AAGACTATTTAAATC[A/C]TATTAGGCTTTTTAT | 55120 |
| rs568221238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175244 | TTCTGAAACTATTAC[A/C]ATCAATAGAAAAAGA | 55120 |
| rs568233855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206195 | ATGGACGTGAAAGAG[A/G]TTTAAGAAACAGTAA | 55120 |
| rs568270655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58198805 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 55120 |
| rs568288142 | in-del | -/TAC | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58230555 | CTGTTGTGCTCCCGA[-/TAC]TATTAAGTAACTCTT | 55120 |
| rs568298627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238357 | TCCAAGTTGTTCGCA[A/G]ATTTCAAATCCACAG | 55120 |
| rs568313544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205527 | CTGACTCTTAAAACT[C/T]CCACACTTCAGATTC | 55120 |
| rs568355480 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58234365 | AAAAACACAAAATTA[C/T]ATGAAAGTGAAGGAA | 55120 |
| rs568377734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174886 | ACAAAATTGATAGAC[C/T]GCTAGCAAGACTAAT | 55120 |
| rs568395296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236602 | CAAACAGAAAACACA[C/G]AGCAAGAGTAGATTT | 55120 |
| rs568427808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211400 | AGTGCTGGGACCCTG[C/T]GCCCACTTTTTCCTC | 55120 |
| rs568428753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179843 | CATCTGACAAAGGGC[C/T]AATATCCAGAATCTA | 55120 |
| rs568432211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58237529 | ATCTCATATCAATAA[C/T]CTTCCATCTAAAGAA | 55120 |
| rs568449364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224497 | TTAAACTATTATTCT[A/G]ATCTCACACATTTAA | 55120 |
| rs568466531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211831 | AGTTCCCAACAAATT[C/T]CTCACCTCCATCTGA | 55120 |
| rs568468995 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179960 | TATGCGGCCAACAAA[A/C]ATATGAAAAAAAGCT | 55120 |
| rs568512069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231042 | TTGTAATCCTCAGCA[C/T]TGCTAACCATGCCTT | 55120 |
| rs568543095 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242576 | CACAGGAAAGAAATA[G/T]CCTTATCTCTAAAGA | 55120 |
| rs568545826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58180222 | CAATCCCATTATGGG[A/G]TATATACCCAAAGAA | 55120 |
| rs568594177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217612 | AAAGAAACATGTCCT[A/G]ATAACAAAAGGGAAA | 55120 |
| rs568626296 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180972 | TACTGTCAGTGCGCA[A/T]GTAAATGGCACAACT | 55120 |
| rs568659825 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194426 | ATTTTGAAGCATTTG[C/T]GATGTTAGAAAGTAG | 55120 |
| rs568675249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215882 | ATAAGAGGATAAAAA[C/G]TCAAGCAGAAAGGCA | 55120 |
| rs568691671 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226933 | GAAGTATCGGTCATC[A/G]ACTTTACTACTCCTA | 55120 |
| rs568713154 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58166013 | CAGTAAACAGTAGTC[A/G]ACTCTCCCTGCTTCA | 55120 |
| rs568722984 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58216677 | GGATGCCAAAATATA[A/C]GATCATATGACAATA | 55120 |
| rs568735594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204006 | GGCTTTCCAAAATCA[A/G]TGTTTTAAAGCATGA | 55120 |
| rs568800792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221827 | AAGGATCAAATACTC[C/T]AGTTACAATTAAACA | 55120 |
| rs568949030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174679 | TAAATGCCCACAAGA[A/G]AAAGCAGCAAAGATC | 55120 |
| rs568949752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58165507 | TGAATGTTACCTCCA[C/T]TGGATCATCACCTTT | 55120 |
| rs568952902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170565 | CCAATTAAAAGACAC[A/C]GACTGGCAAATTGGA | 55120 |
| rs568961545 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58188048 | CTTCTAGAAGCTTTA[G/T]ATTTATGTTTTTACA | 55120 |
| rs568963489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195419 | TGAAGAAGACACATT[C/G]AAATTGTATAAGCAT | 55120 |
| rs568972245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203609 | CTATCCTATAAGGGA[A/T]CTATAAATAGAGGCA | 55120 |
| rs569011174 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184078 | GAAGTAGGTATTGCT[G/T]TCCCCTTAAAAGTAC | 55120 |
| rs569033812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210229 | AAAAGAAAAAGGCTT[A/C]ATTGGACTCACAGTT | 55120 |
| rs569046655 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58229279 | TTGCTTCAGTAACTG[A/C]TTTTTTTTTCTAATC | 55120 |
| rs569062899 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58178992 | TCACAATTGCTTCAA[A/G]GCGAAGAAAATACCT | 55120 |
| rs569084618 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179115 | AAAACATTCCATATT[C/G]ATGGATAGGAAGAAT | 55120 |
| rs569102973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58178576 | AGGTGTTGATGGAAC[A/G]TATCTCAAAACAGTA | 55120 |
| rs569110010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58236113 | CAAATTAAATGAAAA[C/T]ATATACTCAGAGATC | 55120 |
| rs569115102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174309 | GAAATCTACAGAACT[C/T]TCCACCCCAAATCAA | 55120 |
| rs569120692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194870 | GGAAGACAGGGACCA[C/T]AAGGAAAATTACCCA | 55120 |
| rs569173220 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207782 | GTCTGTTTCATGTCG[C/G]GCATAATGACTCATG | 55120 |
| rs569183812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173390 | GCAGCCAGAGAGAAA[C/G]GTCGGGTTACCCACA | 55120 |
| rs569240715 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164560 | ACTTGTTCAAAACTT[C/G/T]GTCTTAAGAAAGCAA | 55120 |
| rs569336959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58209177 | CTTGCCAAACACATA[A/G]TAAACTTTTTAATAA | 55120 |
| rs569350917 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235440 | AGACTAACTACCTTA[C/G]ACTAAAGTCTGCTCT | 55120 |
| rs569351533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173085 | GAAGGGAAGCTTAGA[C/G]AAAAAAGAATAACAA | 55120 |
| rs569352488 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241346 | AACACAGAAAAGCTC[C/T]AGACCTGCTGGGTCC | 55120 |
| rs569413378 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58177353 | TTATTGCAGCACTAT[G/T]CACAACAGCAAAGAC | 55120 |
| rs569515888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240964 | AACTCGGGGAAGGGC[C/T]AGGGAGAGAGGAGGC | 55120 |
| rs569525476 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58202230 | TTATATATACCTATA[A/C]CTTTTTCCTAAAAAA | 55120 |
| rs569529822 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58175586 | ACAAAATTCAACAAC[A/G]CTTCATGCTAAAAAC | 55120 |
| rs569562429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207962 | TATTCAGGAAACTGA[A/G]GCAGAAGGTTTGCTT | 55120 |
| rs569582635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208540 | TCATAAAATACTGCA[C/T]TTATATTGACCAAGA | 55120 |
| rs569594126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239404 | TCATCCAAACCCAAA[C/T]TGAGATACATTCTAC | 55120 |
| rs569635476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240084 | TAACAGTATTTTGCC[G/T]AAAATTAGGTATAAC | 55120 |
| rs569647211 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190835 | CAATTCTATATCTAT[C/G]TAATAAATTGGTTTG | 55120 |
| rs569656927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182591 | TATACAACTAACCCA[C/T]GGAAGAAACAGTTTT | 55120 |
| rs569680735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214261 | CTTTCATCTATTATC[A/G]AAGTTAGAAATCTGT | 55120 |
| rs569696537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182001 | ACACAAATACGTCTT[A/C]TCAGAAAAAAAGCTC | 55120 |
| rs569712852 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58223920 | ATTATAGTATAGGAA[A/C]CCTATTACTTACAAT | 55120 |
| rs569723251 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223778 | TGTTCACTTGTTAAA[C/T]ATATACTGAACTCCC | 55120 |
| rs569739372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187062 | CAGCAATCCCATGAC[C/T]GGGTATATACCCAAA | 55120 |
| rs569764238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162296 | CTTCACAAACACTTA[C/T]ATCAAGCTAATCAGT | 55120 |
| rs569777000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181516 | ACTGTTTCCAAATTT[C/T]ACAAAGAACTGAACT | 55120 |
| rs569778303 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196144 | AAAAGAGACTGCAAA[C/T]ATGGCATAAACAAAT | 55120 |
| rs569800007 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215399 | TATCATAATATAGTA[C/T]ACTTACAATTATATG | 55120 |
| rs569825853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163307 | TACTGGGCAACAAGA[A/G]CAAAACTCCGTCTCA | 55120 |
| rs569845607 | in-del | -/CT | | | intron-variant | FANCL | GRCh38.p7 | 2:58191767 | CTTTGCCCATATTAG[-/CT]CTCTCACTATATTAA | 55120 |
| rs569858511 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | FANCL | GRCh38.p7 | 2:58194007 | CTATGTAATAGGACT[G/T]ACTCCTTTAATTACA | 55120 |
| rs569863600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187368 | AGAACTGAACAATGA[A/G]AACACTTGGACACAG | 55120 |
| rs569868019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232992 | AAAAACAGAGGAACA[C/T]AATTAAATGTACCCT | 55120 |
| rs569887524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58219284 | GCTAGAACAAATTGA[A/G]CAAGAAAATAAAATA | 55120 |
| rs569917220 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58193719 | AGAAAAAGAATCCAG[C/T]TGGTCAAAAGAACTT | 55120 |
| rs569946109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162782 | CTAATTCCCTCCTTT[C/T]TCAGCCTCATTTTTC | 55120 |
| rs569955377 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230549 | TGACCTCTGTTGTGC[C/T]CCCGATACTATTAAG | 55120 |
| rs570011159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58207082 | CCTTGCAAGGAGGTG[C/T]TGGCATATAACTACA | 55120 |
| rs570012187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225142 | GCTGACCAAAAAAAT[A/G]GGACAATTTAAGCAT | 55120 |
| rs570046360 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212173 | GCTGGGGAAGCCTCA[C/G]AATCATGGTGGAAGG | 55120 |
| rs570051169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58218441 | CAAAAAACTCATGTG[A/G]AAAGAAAAAGGCAGC | 55120 |
| rs570110490 | in-del | -/ATA | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58194009 | TGTAATAGGACTGAC[-/ATA]TCCTTTAATTACAAA | 55120 |
| rs570154517 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58183365 | GTGTAGGTCTGAATT[A/C]TCCAAAGTAGCTTTT | 55120 |
| rs570165752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198127 | GAGGGAGAAAGAAAA[C/T]GGACATTAACTGTAA | 55120 |
| rs570176536 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58172728 | TCTAAAAAGCAGAGC[A/G]CCTCTCCTCCTCCAA | 55120 |
| rs570179010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212721 | ACCAAGACATCATTT[G/T]GTATCACTTACCTTT | 55120 |
| rs570217357 | in-del | -/A | 0.00193567 | 0.0310498 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162961 | CCTGAAAGCATGGGG[-/A]AAAAAAATTATGCTG | 55120 |
| rs570251839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58220835 | CACATTGTACCTAAG[C/T]TAGCCCTCGATTTAT | 55120 |
| rs570291000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204749 | GCTGTATAAGCACAG[A/G]TACAGCCTGGTCTCC | 55120 |
| rs570303840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58176177 | CATGGGTAGGAAGAA[A/T]CAATATCATGAAAAT | 55120 |
| rs570312234 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58222770 | AGACAGCTTATTTGG[-/A]AAGTAAAAATAAATC | 55120 |
| rs570314114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231512 | TCACAAAATCCTCTC[A/G]ATTCTACTCATAAAT | 55120 |
| rs570347268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191869 | AAAAGGATTTTCATA[C/T]ACAACACCCCAATTT | 55120 |
| rs570364359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175685 | CCAATATCACAGTGA[A/C]TGGGCAAAAACTTGA | 55120 |
| rs570379670 | in-del | -/AGTT | 0.00253914 | 0.0355404 | intron-variant | FANCL | GRCh38.p7 | 2:58164813 | TTCCAAATTAAACAC[-/AGTT]AGACTTTTTGAAACC | 55120 |
| rs570386356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175161 | CTTACCAACCAAAAA[C/G]AGTCCAGGACCAGAT | 55120 |
| rs570434874 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227566 | TGCCGGCATGCTGAA[A/G]TCTATCGGTGTGCTC | 55120 |
| rs570473909 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197791 | ACAATAAAAATGGAG[G/T]AGAAATGCCAAGGTT | 55120 |
| rs570500893 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231068 | GCCTTGCTTAAGCCT[C/T]TCTTTATTTGGCTTG | 55120 |
| rs570551277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174923 | GAGAGAAGAATCAAA[C/T]AGATGCAGTAAAAAA | 55120 |
| rs570575233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160768 | ATTTCATGATTTTAT[A/G]TAAGGTAAATAGATG | 55120 |
| rs570582054 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58177817 | AGAAAAAGAAAAAAC[-/A]AAAAAAACCCAAATA | 55120 |
| rs570642784 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58205472 | AGAATGTCTTTATCA[C/G]GTTTTACCATATGAC | 55120 |
| rs570669373 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203324 | TTAAATGCCAGACAC[A/G]TTTTTAAAAAGGACA | 55120 |
| rs570702854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211358 | GAGCAGCTGGGATGC[A/G]GGGAACCAAGTCCCT | 55120 |
| rs570718666 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236023 | ATGTATTTGGAGTGC[C/T]CAACACAGAGGACAG | 55120 |
| rs570750083 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195243 | CTATCAACACTCTTA[C/T]CATGTCTAAAAGACT | 55120 |
| rs570765937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217531 | GCAGTTTTTAAAATA[G/T]GTAACTAATTAGCTT | 55120 |
| rs570786939 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159234 | TCAGGAAAAATAACA[C/T]GCAAAAACTTGATCT | 55120 |
| rs570795184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165370 | ACTAATCTGAGAAGA[C/T]TGTAAGCTTCACAAA | 55120 |
| rs570797875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216791 | ACCTCACCTACAACT[A/G]GGATGTACCTAGAGA | 55120 |
| rs570828910 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58224430 | TTTGATAACCCTTAT[G/T]AATTAGGATTTATGA | 55120 |
| rs570851560 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58198246 | AATGACTACCTAAGT[-/A]AAAACAGTTACAGTT | 55120 |
| rs570896110 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218459 | AGAAAAAGGCAGCAT[C/T]ACTATAGATCCTAAA | 55120 |
| rs570913177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236529 | AACAGAATTACAAAA[A/C]AGAATTCCAATAATA | 55120 |
| rs570955552 | snp | A/C | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158919 | CTTTGCCCACTGTAC[A/C]GTGGACACTTCTCAG | 55120 |
| rs570957262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230245 | ATGTATTTGAAAAAG[C/T]ATGTGTAGCAATATT | 55120 |
| rs570959436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164759 | ATTTTCATTCTTAGT[A/G]TCTACTTGTTCACAA | 55120 |
| rs570994029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223623 | AAGAGGCAAAGGTAC[A/G]TAGCGGAAAGGCTTC | 55120 |
| rs571015835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189496 | TTTTATATGTATATA[C/T]AGATACATAAATGTA | 55120 |
| rs571018517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58229548 | TCTCAGAAGAAAAAT[C/T]ACTGAAGAAGTGATG | 55120 |
| rs571077381 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242401 | TATGTAGAAATACAA[G/T]TTTTCACCGCTGATG | 55120 |
| rs571113066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58196212 | TTTGGGTAAACAGTT[A/G]CTACTTAAAGGGAGA | 55120 |
| rs571138645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58210069 | TATATTGTTTAAAAA[A/G]GACAAAAGTATCAGC | 55120 |
| rs571206553 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210491 | ACACAGAGTCAAACC[A/G]TATCATTCTACCCCT | 55120 |
| rs571240597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221265 | TAGAAAGGTTATAAT[A/C]CACTTAATAATAAAT | 55120 |
| rs571244895 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232975 | TCCCTCAAAGCAGTT[C/T]CAAAAACAGAGGAAC | 55120 |
| rs571266013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174203 | GGGAGAATTTAACAC[C/G]CCACTGTCAACATTA | 55120 |
| rs571280639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58203534 | ATTCACAATTTAGAA[A/C]TAAAAAATAAAGATG | 55120 |
| rs571293343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173914 | AAGCAGAGACACACA[C/T]AGGCTCAAAATAAAA | 55120 |
| rs571330868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170251 | ATTCTTAAAGAAAAG[A/G]ATTTTCAAACTAGAA | 55120 |
| rs571450270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235417 | AGAAGGTGTTGCTTC[A/T]CTTGTAGAGACTAAC | 55120 |
| rs571450894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58201962 | TACTTTGAGGTATGT[C/T]ATTAATAAAAAAAAT | 55120 |
| rs571462973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183295 | TTTAGAGATTATTTC[A/T]CTAATTGCAGAGCTT | 55120 |
| rs571490062 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58207883 | GCGACACAGTGAGAC[C/G]TCATCTTTACAAAAA | 55120 |
| rs571567400 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178449 | AATCAATAAACGTAA[C/G]CCATCACACAAACAG | 55120 |
| rs571598670 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58194789 | CAAATGAATATGTCA[C/G]AGCAGCAGCAGCAGA | 55120 |
| rs571605217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194292 | GACAAAAGGAATTTC[A/G]TTTTTTTATAATCAT | 55120 |
| rs571620651 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58168110 | AGGGAGATGAATTCT[C/T]TAAAAAATATTTTTA | 55120 |
| rs571669076 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58172036 | CTGCAAGGTGGCAGC[A/C/G]AGGCTGGGGGAGGGG | 55120 |
| rs571820295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172847 | CTACTATGAGCTACA[A/G]GAGGAAATTCAAACC | 55120 |
| rs571857918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58169210 | TTCCAGAGAAAGGAA[C/G]AGGCAGCAAAATCTT | 55120 |
| rs571908691 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192845 | AGGCTATGCTGTTTT[A/T]TCTAAAAAGAAAACA | 55120 |
| rs571919257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173054 | GACGGAAGATGAAGT[A/G]AATGAAATGAAGCAA | 55120 |
| rs571929727 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205158 | AGCCTCCTAACTTAG[A/G]AAATATATTTTTTAA | 55120 |
| rs571946278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172157 | TGCCTCTGTAGGCTC[C/T]ACCTCTGGGGACACG | 55120 |
| rs572005294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175791 | TGGCCAGGGCAATTA[C/G]GCAGGAGAAGGAAAT | 55120 |
| rs572005576 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | FANCL | GRCh38.p7 | 2:58176361 | AGCTGGAGGCATCAC[A/G]CTACCTGACTTCAAA | 55120 |
| rs572025197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161703 | TCGTTGTACATATTT[A/G]GGAGGGTATGTGTGA | 55120 |
| rs572061771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161049 | ACTCAGATCACAAAA[A/G]GCATTCTTCTCAACA | 55120 |
| rs572107375 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168283 | CTGGTTAGATAGTGG[A/G]TGCAGCCCACAGAGG | 55120 |
| rs572143438 | snp | A/C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58188105 | TTTTGTATATGGATC[A/C/G]ATGAGGTCATTTTCA | 55120 |
| rs572216474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166891 | TCCACTGTGCTGGAT[G/T]CAACTGTTCTAACCT | 55120 |
| rs572228962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58225484 | ACAGGCAATGATTGT[C/T]ATTAGAGGCTAAAAT | 55120 |
| rs572330172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197462 | TGTTCTCTCCATTTT[A/G]CTATCAACTGCCACA | 55120 |
| rs572351598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192144 | TTAAAAAAACCTGTT[C/T]CATGCAACTAGTTTC | 55120 |
| rs572352561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231267 | GTCTCAAATCCTTCA[C/T]CTGTTGTAACTTCCA | 55120 |
| rs572392708 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58237981 | AGATCCATGTGGTGA[A/G]GAACTAAGGCCTCCT | 55120 |
| rs572435823 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58186022 | ATTACCCACTGTTAG[C/T]TATACAGTAGTCACA | 55120 |
| rs572456649 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 2:58243443 | TATTTCTTAGTTATG[C/G]AGGCTGAGAAGTCCA | 55120 |
| rs572469329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163376 | TCTAATAATTTAACA[A/G]TGCTAGGCAAGGATT | 55120 |
| rs572552754 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58175005 | AGAATACTATAAACA[C/G]CTCTATGCAAATAAA | 55120 |
| rs572587099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171263 | TGAACAACCTTCTCC[C/T]GAATGACTACTGAGT | 55120 |
| rs572590601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236395 | CATAAAAAATGGAAT[A/C]CTAATATTACGTTAA | 55120 |
| rs572623932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58229751 | AAGCAGGTCTTTAAA[A/G]AACAATAAATTTAGT | 55120 |
| rs572647027 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211114 | CTTCCCTTCCGCATT[C/G]TCCTAACAGAGGTTC | 55120 |
| rs572667302 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58169595 | GAAAGTGGGTAATAA[-/C]AAACTCCTCTGAGCT | 55120 |
| rs572681764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217032 | GGAATTGCAGACTCT[A/G]TATGACTGAAATAAA | 55120 |
| rs572682934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58204487 | TGGTCAGTGAGCACT[A/G]TGTTTCAGTTTTCCA | 55120 |
| rs572684769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211448 | TTATGTGAGTGGCTG[A/C]CGTGAAGACCTCTGG | 55120 |
| rs572734402 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58185332 | GACTGTTCCGTATAC[A/G]GGCTTGTCCATGAAA | 55120 |
| rs572738548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179520 | ACGGTGTTGGGAAAA[C/T]TGGCTAGCCATATGC | 55120 |
| rs572749995 | in-del | -/ACTT | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162291 | AACTGCTTCACAAAC[-/ACTT]ACATCAAGCTAATCA | 55120 |
| rs572778461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190637 | CTAAAATCAATGAAA[C/T]AAAAAAAGATCATAA | 55120 |
| rs572793883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209684 | TTTGAAATCTTTATT[A/G]TTAGGCATTATTAGC | 55120 |
| rs572832609 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58203192 | ACCTACATACATATT[A/C]TGTGTGTGAGAGAAT | 55120 |
| rs572868322 | snp | A/G | 1.6531e-05 | 0.00287493 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159438 | AATCAGCTATACACA[A/G]TTCCCAAACTCATTT | 55120 |
| rs572874753 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58204617 | ATACAGTATGAGACT[G/T]TAATGCTCCCTTTGT | 55120 |
| rs572895501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184922 | CCTTCCACAAAAGGT[A/T]TGCAGCAAAGGTCCG | 55120 |
| rs572899334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179175 | AAGTAATTTATAGAT[C/T]CAATGCTATCCCCAT | 55120 |
| rs572924686 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164236 | GTAACTGCTTAAGAT[C/T]AATTTGGATTTCATT | 55120 |
| rs572958804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196315 | TATTTTTAAGACAAA[A/G]AGAAATATAGATGTA | 55120 |
| rs572963445 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58195978 | GTTCACTGCAGCACT[C/G]TTTGTCAGAATTTGT | 55120 |
| rs572963676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195825 | GGGAATATAAACTTA[C/T]ACAACAATCTAGGGA | 55120 |
| rs573064544 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58193302 | ACAATTATACAATGA[C/T]ACCTCAATACTACTG | 55120 |
| rs573066415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58220935 | GTGATAAGAATTGCC[A/G]GGCGTGGTGGCTCAC | 55120 |
| rs573083133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188172 | AAAGACTGTCCTTCC[C/T]CCACTAAACTATCTT | 55120 |
| rs573103330 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218906 | GGTTATATACAAAAA[C/T]ATTTACAAGTATGTA | 55120 |
| rs573103849 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241523 | TCCCCAACCGGTAGT[A/G]GGAGGGAAGATTGCC | 55120 |
| rs573110316 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58215185 | CTAGGTCCATGACAT[C/T]AATGCCTCAAAACTA | 55120 |
| rs573120248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165625 | TTTAATAGTTGACTT[C/T]ATATAAAGAAGTCTG | 55120 |
| rs573144891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170341 | AAGCAAATCCTGATA[G/T]ATCTTGTCACCACCA | 55120 |
| rs573183499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58164900 | TAATACCACGTATGT[A/G]ACATTCTTCCCCCAG | 55120 |
| rs573183541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170704 | GAAAGCAAAAAAAAA[A/G]AAAAGCATGGTTTGC | 55120 |
| rs573188785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173982 | AAAAGGCAGGGGTTG[C/T]AATCCTAGTCTCTGA | 55120 |
| rs573189076 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58173630 | CGAAAAGAGCTCCTG[A/T]AGGAAGCACTAAACA | 55120 |
| rs573214063 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224663 | AAAACTTTCCATTGT[A/T]AGCAATATTAGTATT | 55120 |
| rs573225884 | in-del | -/GAG | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58227910 | GAAGAAGAGAAAGAA[-/GAG]GAGGAGGAGGAGGAG | 55120 |
| rs573227103 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196083 | AATAAATATAGTAGA[C/T]AAACATAAGATTATG | 55120 |
| rs573273746 | snp | C/T | 4.77635e-05 | 0.00488666 | intron-variant | FANCL | GRCh38.p7 | 2:58221892 | AGAAATACATTAAGT[C/T]AAAATATATAAAACA | 55120 |
| rs573283224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221462 | TCATTTTTTTCAAAG[A/G]AAGCTGGATGATTCT | 55120 |
| rs573370745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173121 | GAACAAAGCCTCCAA[G/T]AAATATGGCACCATG | 55120 |
| rs573408957 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58169400 | AAACCCCATATGAAA[A/G]TCAACAATATCAAAG | 55120 |
| rs573443278 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58241027 | CCTCGCTCCCCATCC[A/C]GCGCGGCGACCACCG | 55120 |
| rs573464226 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211241 | TTCTGGACTTCTGTG[C/T]ACCCACAGGCTCAAC | 55120 |
| rs573466203 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182146 | CTTCAACTATGGATA[C/T]AGGTAAGAAACCACA | 55120 |
| rs573502350 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207152 | TTGGGGGTTCATTTA[G/T]AACAGAACTATGCTT | 55120 |
| rs573536494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163610 | GTCTGGCTACCTATT[A/T]CACTGTATACCCACG | 55120 |
| rs573562752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234522 | AACACAGACCCAAAA[A/G]AGTCCAGAGTACATA | 55120 |
| rs573565636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202104 | TTCTTTTTTTTTCCC[C/T]AAAATTTTTGTTTCC | 55120 |
| rs573590808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194427 | TTTTGAAGCATTTGT[C/G]ATGTTAGAAAGTAGA | 55120 |
| rs573626130 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184027 | CTTCCAGGTATAGAA[C/G]TCAAGAATTCTAAAT | 55120 |
| rs573725826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240511 | TTTCCCATACCTTGA[C/T]TTCTTCAACTAGAAA | 55120 |
| rs573754946 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58233256 | AAGAACTATTCTATA[C/T]AGAAATCTGTGCTGT | 55120 |
| rs573774147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58177065 | TCAGAGAAATGCAAA[C/T]CAAAACCACAACGAG | 55120 |
| rs573775669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207619 | CTTTGTTAATAGTGG[A/C]CTAGCCTATGATATA | 55120 |
| rs573788864 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | FANCL | GRCh38.p7 | 2:58177398 | AATATCCAACAATGA[C/G/T]AGACTGGATTAAGAA | 55120 |
| rs573799665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239555 | AGGGGATGGGGGTAT[A/G]AAACATACAACTGTA | 55120 |
| rs573799851 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58232569 | TTTCTAAATTTTAAT[A/G]AAATGAAAATATATT | 55120 |
| rs573810372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208005 | TTGAGGTTGCAGTGA[A/G]CTATGATGGCACCAC | 55120 |
| rs573837485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181588 | GTATTCAGATACCTG[A/C]AAGTTACTTTGTATA | 55120 |
| rs573858727 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58227160 | CTAGGGGAGCATACA[A/G]ACGGGCAGGCTGTGG | 55120 |
| rs573885787 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179553 | AAAACTCAAACGGGA[C/T]CCCTCCCTTACACCT | 55120 |
| rs573895358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220211 | TGGCTCTTAAGTACA[A/G]ATCGTACACACTTTG | 55120 |
| rs573943488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238539 | AATCAGAAACCTAGA[C/T]GAAACTAACAAATTC | 55120 |
| rs573992496 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58226510 | GTGTCAAGAATACCT[A/C]GTTTATAATACAATC | 55120 |
| rs574048703 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58201138 | GTAGATGACTAAATA[C/G]AATATAAGAAAGTAA | 55120 |
| rs574049145 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211611 | TGCAAATTTTTTGAA[A/C]TTTTATTTTATGCTG | 55120 |
| rs574066750 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180274 | AGACATGCATACATA[G/T]GTTTATTCCAGCATT | 55120 |
| rs574076259 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58179373 | AACAGCATGGTACTG[A/G]TACCAAAACAGAGAT | 55120 |
| rs574154093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186123 | GGGCAAGGAAATAAT[G/T]TGAGAGAAGCCTAGT | 55120 |
| rs574181289 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213059 | GCAAGGCCAGCATTA[C/T]CTAACAAGGATTTTT | 55120 |
| rs574213615 | in-del | -/TGTG | | | intron-variant | FANCL | GRCh38.p7 | 2:58203193 | CCTACATACATATTC[-/TGTG]TGTGAGAGAATTAGT | 55120 |
| rs574280079 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240330 | AGACTATGCGTGATG[A/G]TGGGGAAGTGGGCAC | 55120 |
| rs574348425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175354 | AATTTTACACCAATA[A/T]CCTTGATGAACATTG | 55120 |
| rs574355109 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216003 | CCAGGATCTCTGTGG[A/G]AACTCTTGAAAGACT | 55120 |
| rs574358359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172063 | GGGGCGCCCGCCATT[A/G]CCCAGGCTAGCTTAG | 55120 |
| rs574371013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180419 | TTCATGTCCTTTGCA[G/T]GGACACGGATGAAGC | 55120 |
| rs574391873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172358 | GGCACCGCCCAGTAG[A/G]GGCAGACTGACACCT | 55120 |
| rs574393932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58167436 | GTCTGTTTCTACATG[G/T]GTATTTAAAATCCGT | 55120 |
| rs574431166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224653 | AAGAAATATCAAAAC[G/T]TTCCATTGTTAGCAA | 55120 |
| rs574441642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190830 | TTTTCCAATTCTATA[C/T]CTATCTAATAAATTG | 55120 |
| rs574452757 | in-del | -/AATA | | | intron-variant | FANCL | GRCh38.p7 | 2:58190775 | TTTAATTAATTAATT[-/AATA]CTGTCTCAGTGTCTC | 55120 |
| rs574454569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231621 | TTCAGTCTCATATCC[C/T]GACTAGTTGTATCTA | 55120 |
| rs574560056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170858 | ACCCAATACAGAAGC[A/C]ACCAGATTCATAAAG | 55120 |
| rs574574920 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58171678 | TCCCAGGGTGAGCGA[C/T]GCAGAAGACGGGTGA | 55120 |
| rs574599026 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58171221 | GGATTAAGAAACTCA[C/T]TCAAAACTGCACAAC | 55120 |
| rs574599745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58196323 | AGACAAAGAGAAATA[C/T]AGATGTATCTGAACC | 55120 |
| rs574613670 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168747 | AGTAGACCTGGGGCA[C/T]TCAAGCTTGGTGGGG | 55120 |
| rs574614843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58207069 | TTGTCCTAGCTGCCC[C/T]TGCAAGGAGGTGTTG | 55120 |
| rs574655745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166789 | GCCACTTCCTTAAAC[A/G]TGTATTTTATACCTA | 55120 |
| rs574659785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160880 | AGGAAGACTGAAACC[A/G]AAGGCAACATACAAT | 55120 |
| rs574680429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230734 | TTCATTCAAATGTCC[A/C]TTGGTAACCCCTGCT | 55120 |
| rs574714203 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58204331 | GCTATATTCCTATTA[A/C]TCCATTATAAAAATC | 55120 |
| rs574721088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174534 | AACCTGCTCCAGAAT[C/G]ACTACTGGGTACATA | 55120 |
| rs574750839 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58197061 | ATAGTATTTTACTTA[G/T]AGCATACATCAAAAT | 55120 |
| rs574787901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204854 | ATTCTAAACATATAG[C/T]ACAAGCACAACTGCT | 55120 |
| rs574875457 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58188127 | TCATTTTCACTTACA[A/G]ATATCTAATTGTCTC | 55120 |
| rs574914375 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242681 | CTTTGTCCAACCGTA[A/C]TTCCCCACAACTGTC | 55120 |
| rs574925264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179134 | GATAGGAAGAATCAA[A/T]ATCGTGAAAATGGCC | 55120 |
| rs574938099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58236294 | AAAAGAGCAGAGATT[A/T]CTCGTAGAAAACAGT | 55120 |
| rs574958628 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241436 | GGAAGATCCTGGAGG[A/C]TTCCGCGGGCGGAAA | 55120 |
| rs574976980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58216861 | GCACGGGGGTAAAGC[A/G]GGTGAGGAGAAGAGG | 55120 |
| rs574979506 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158811 | ATATTAATATCTATT[C/T]GGTCTATACTGGTTC | 55120 |
| rs574986407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184431 | TTGAGTTTTGGAATA[G/T]GTTTTGAACCACAAA | 55120 |
| rs574995941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235660 | CCTGCAAAGAAGCAA[C/G]GCAATACCCACAATG | 55120 |
| rs575045198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58223072 | GAACAGATATTACAA[A/T]ACAGCACTTCAAAAC | 55120 |
| rs575073708 | in-del | -/AAAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58239575 | ATACAACTGTATCAT[-/AAAC]AAAATTTGAAATATG | 55120 |
| rs575123869 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172868 | AATTCAAACCAAAGG[C/T]GAAGAAGCTGAAAAC | 55120 |
| rs575177878 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58214546 | GACAGGGTCTCACTG[A/T]CACCTAGACTGAAGT | 55120 |
| rs575194035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214024 | ACCCAGCCCTGTCTA[C/T]ATACACTTGTTTTAT | 55120 |
| rs575194077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221334 | ATTCAGAAACTGAAT[A/G]GCAAACAAATCATCA | 55120 |
| rs575242941 | snp | C/G | 1.67773e-05 | 0.00289626 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159379 | AGACAGAAATATCAA[C/G]AGTCTCAAGAACCTT | 55120 |
| rs575266960 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206616 | AGAAATAAAAGCTCT[C/T]TAGTTCTTTGTTTGT | 55120 |
| rs575285333 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167478 | CCTTTGTATACCCAA[A/G]ATAAGGTTAACTCCC | 55120 |
| rs575318255 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227392 | GATCACATGTGGGCT[A/T]GGAGAATGAGTGCAA | 55120 |
| rs575327472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189671 | ATCTTTAAAAGCATT[C/T]TGTTACTTTCATAAT | 55120 |
| rs575362230 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58203129 | ATAATGAGATTTCCA[A/T]CCCACTAATTTTTTC | 55120 |
| rs575409102 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58194413 | GCATTAAGGATATAT[G/T]TTGAAGCATTTGTGA | 55120 |
| rs575428524 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58213962 | GCTGCCCTATGGGAC[-/A]ACTCTAGGGAGCATC | 55120 |
| rs575438360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164339 | AAATGCAGTTATTGC[A/G]TATCTGGCAAAAAGA | 55120 |
| rs575460078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195699 | ATAAAATGTTTATAA[A/T]AAAAGGAAAAAAATA | 55120 |
| rs575483324 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201246 | CTTTTCCTTTCAAAA[G/T]TAATTTACAACAACA | 55120 |
| rs575521752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208984 | AGTCAAAAAATAAAT[A/T]GCACATTTCTATTGC | 55120 |
| rs575522327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58195027 | ATTTTTAAAAAATCA[A/G]TTATCTGAAATCTAT | 55120 |
| rs575536193 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228546 | CCATACACATTCACT[C/T]ACCTCTTGTCTATGG | 55120 |
| rs575562041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175702 | GGGCAAAAACTTGAA[G/T]CATTCCCTTTGAAAA | 55120 |
| rs575579370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173539 | TCCAGCCAAACTAAG[A/C]TTCATAAGTGAAGGA | 55120 |
| rs575616190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173964 | AAGCAAATGGAAAAC[A/C]AAAAAAGGCAGGGGT | 55120 |
| rs575670876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227649 | CCGATATATTTCTCT[A/C]AACGTCCAGCCACTT | 55120 |
| rs575699463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172542 | CTGCAGCTGAGGGTC[A/T]CTGTTAACAGAGGGT | 55120 |
| rs575700280 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58177569 | TCTCACTCATAGGTG[A/G]GAATTGAACAATGAG | 55120 |
| rs575727243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187178 | CCCAAATGTCCATCA[A/G]TGATAGACTGGATTA | 55120 |
| rs575810554 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58187504 | AAACCAACATGGCCC[A/C]TGTATACATATGTAA | 55120 |
| rs575862199 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58176471 | AGCCCTCAGAAATAA[C/T]GCCGCATATCTACAA | 55120 |
| rs575887634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200978 | TCAATTTTGTTTATA[C/T]AACAAACCTCACATA | 55120 |
| rs575916313 | snp | C/T | 1.79326e-05 | 0.00299432 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163104 | AAAAAAATTTAATAA[C/T]TGCATGCTCTACTCT | 55120 |
| rs575951427 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58166143 | ATGCTTGATATACTA[A/C]ACGTATGCAATAGTA | 55120 |
| rs575963592 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234285 | AACTAAAATGAGAAA[C/T]TGTATTTTAAAAAAT | 55120 |
| rs576014162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240366 | TGAGTGTAATGGTCA[A/G]AAAGGAAAAGTCTAC | 55120 |
| rs576069231 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58238597 | ACTCAAAAGGAAAGA[A/G]AAAATCTGATAATAG | 55120 |
| rs576093750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206852 | AGGTACATTTTACCC[A/G]TGCTGCTTCCTGGTC | 55120 |
| rs576114611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161769 | ATCAGGATAATTAAG[A/C]TATTCATCACCTCAA | 55120 |
| rs576121305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58211566 | TTCTGCTCAGAAAAC[A/G]GGATTTTCTTTTCTA | 55120 |
| rs576123484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58213300 | TAGCAATTCTAGTAT[A/G]TGGACAGCACAGTTC | 55120 |
| rs576132993 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58213027 | TAGAAATACCAAATA[C/T]GTAATTTAAAAACAC | 55120 |
| rs576152070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161077 | ACATGAAAAGTAGTA[A/G]TATTGGATATATTCT | 55120 |
| rs576178220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180948 | ACACAAAGCAACTGA[A/G]CTCTCATATACTGTC | 55120 |
| rs576179044 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179848 | GACAAAGGGCTAATA[A/T]CCAGAATCTACAAGG | 55120 |
| rs576203224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220091 | AGAGACTTTAAGCAG[A/T]CCATCTGCAGTGAAA | 55120 |
| rs576212318 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58180517 | AACAATGAGAACACA[G/T]GGACACAGGGAGGGA | 55120 |
| rs576239156 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58236061 | GGAACAAAAAAAAAA[-/AAAG]AAAGAAAGAAAAAAT | 55120 |
| rs576260195 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 2:58243594 | CACTTGCCAAAAGCA[C/G]TTGGCTCCTTGATTC | 55120 |
| rs576263507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232447 | AGTGTTATTTCTTAG[C/T]AAATAAATTTATGAA | 55120 |
| rs576323777 | snp | A/G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58205774 | AGCTGGCAAAAATGC[A/G/T]GTGTTCAGGATAGAG | 55120 |
| rs576372655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186266 | TCAAAAAGCAAACAT[A/C]AGAATTTTCTTTAAG | 55120 |
| rs576388948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224621 | CTAGGAATAAAATGG[C/T]CTCAACAAGGATCAC | 55120 |
| rs576389872 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203886 | GAGTCTATAAAATTG[-/T]TAACTGTAGTATTTG | 55120 |
| rs576391356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58217354 | CAGCAAAGATGTGCT[A/C]CCTCTGGAGGCTCTA | 55120 |
| rs576458485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58167414 | TATCTCTGTTTCTCC[C/T]TTCTCTGTCTGTTTC | 55120 |
| rs576464123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58238500 | GATAATAAGGGATTA[C/T]TGTAAATAACTTTAA | 55120 |
| rs576480131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58192219 | ATCTCATGTGCTCAA[A/G]ATGCACAGATCTCAA | 55120 |
| rs576523667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205164 | CTAACTTAGGAAATA[C/T]ATTTTTTAATATCAC | 55120 |
| rs576553021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58224035 | GAAGAAAGCTAAAAT[A/G]CAGGATTTCATTTTT | 55120 |
| rs576571147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185118 | AACAGGGAAATATTC[C/T]CTGATATGGAATCTA | 55120 |
| rs576599136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58166988 | GGAGGCTGAGGTGCG[C/G]AGATCACGAGGTCAA | 55120 |
| rs576606947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196958 | TTAAAAAAAGGGACA[C/T]GGGTCTCATGAAATT | 55120 |
| rs576614896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172023 | GTCTAAGATCAAACT[A/G]CAAGGTGGCAGCGAG | 55120 |
| rs576641867 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181594 | AGATACCTGCAAGTT[A/G]CTTTGTATAGAACTA | 55120 |
| rs576667300 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58171692 | ACGCAGAAGACGGGT[C/G]ATTTCTGCATTTCCA | 55120 |
| rs576700327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58211565 | TTTCTGCTCAGAAAA[C/T]GGGATTTTCTTTTCT | 55120 |
| rs576710880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58197703 | TCTTTACTCAAAATA[C/T]TGAATGTTCTAAAGC | 55120 |
| rs576766596 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58185462 | ATTTAAACCTTGAGA[A/G/T]CATGAACCATTAGAA | 55120 |
| rs576767523 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58196334 | AATATAGATGTATCT[A/G]AACCAAAAGTGACAA | 55120 |
| rs576772468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175317 | GATACCAAAGCCGGG[C/G]AGAGACACAACCAAA | 55120 |
| rs576803073 | in-del | -/TTTA | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160763 | CTGTAATTTCATGAT[-/TTTA]TATAAGGTAAATAGA | 55120 |
| rs576819503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184998 | GTTGGTATGCCTTAA[C/T]GTGGGGTAGGACTGC | 55120 |
| rs576829263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58203746 | TAAGAATAAGAACTA[C/T]AAAAGAAATTTATAG | 55120 |
| rs576848690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230647 | GGCCTTTTCAAACTG[C/T]CACAACTCTCTCCAT | 55120 |
| rs576866691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171761 | CAGTGGGCGCAAGAC[A/G]GTGGGTGCAGTGCAC | 55120 |
| rs576890951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179088 | AAATAAGAGAGGACA[C/T]AAACAAATGGAAAAA | 55120 |
| rs576903537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58196465 | AACACTCATTACTAC[A/G]AATTCTACATTTTCT | 55120 |
| rs576905755 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232919 | TGAAAAAGTAATAAA[A/G]TTCTCAAAAAACAAT | 55120 |
| rs576927541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58174513 | TCATCTACATGGAAA[C/G]TGAACAACCTGCTCC | 55120 |
| rs576940749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179974 | ACATATGAAAAAAAG[C/T]TCATCATCACTGGTC | 55120 |
| rs576940861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58175031 | ATAAACTAGAAAATC[C/T]AGAAGAAATGGATAA | 55120 |
| rs577010040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237012 | AATCAACAAAGATCG[C/T]TGGAGATTTCAACAC | 55120 |
| rs577029404 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239948 | GATTTAAATAAACTG[C/T]TAAGGCAGGTACAAA | 55120 |
| rs577032625 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58173135 | AGAAATATGGCACCA[C/T]GTGAAAAGACCAAAC | 55120 |
| rs577039302 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58165665 | GTCATTGTTAGATTT[A/C]TTTTCATAATACAAA | 55120 |
| rs577063114 | snp | C/T | 4.96504e-05 | 0.00498224 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160108 | TAACAATTTGCTTAC[C/T]TTACTACAATATGGA | 55120 |
| rs577068223 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58184299 | ATGAGAATCAAAATA[G/T]TTGGATTACATTATA | 55120 |
| rs577071498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236415 | TATTACGTTAAGGCA[C/G]ACCATGATAGATTTA | 55120 |
| rs577176931 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242127 | TTTCCAATGCATCAC[A/G]TTTGAGCCCTACTAT | 55120 |
| rs577206296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170800 | ACATAATGGTAAACG[A/G]ATCAATGCAACAAGG | 55120 |
| rs577233140 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58174043 | AAGAGACAAAGAAGG[A/C]CATTACATAATGGTA | 55120 |
| rs577233560 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58188805 | TTGGGATTTTGATTG[A/C]GAATGCATTGAATCT | 55120 |
| rs577265094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58215282 | TCACCATTGTTATGC[C/T]TAATTTTATTTAAAA | 55120 |
| rs577268399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170366 | CCACCAGGCCTGCCT[C/T]ACAAGAGCTCCTGAA | 55120 |
| rs577279370 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212215 | AAGTCCCATCTTACA[C/T]GGATGGCAGCAGGCA | 55120 |
| rs577330364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164289 | AAATTCCATACACTG[C/T]AGAATAAGCCTTTCA | 55120 |
| rs577344443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163697 | AAGAAGTAATTTTGA[C/T]ATGATTATCATTGAA | 55120 |
| rs577415280 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58223015 | TATATCAATTTTTTT[A/T]AACCAGGATAGGACA | 55120 |
| rs577422116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188813 | TTGATTGCGAATGCA[C/T]TGAATCTCTAGATCA | 55120 |
| rs577450954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235597 | CATGCAACAGGTAGC[A/T]TTCATTATGTCTAGC | 55120 |
| rs577465014 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192794 | GAATCAGCTAACAGC[C/G]AAAAGTGTTTGCCCC | 55120 |
| rs577476743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58222152 | TGCCTAATAAAAGTG[C/T]CTGTTTTTTTACGGA | 55120 |
| rs577545353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194961 | AGATCTTCCAAGTTT[A/T]AAGTCCAGAAACACT | 55120 |
| rs577577230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227572 | CATGCTGAAGTCTAT[C/T]GGTGTGCTCTTGACA | 55120 |
| rs577584491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188331 | TGAAATCAGGTTGTG[A/T]TAGTCTTCTAACTTT | 55120 |
| rs577600082 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58171309 | GCAGAAATAAATAAG[-/T]TTTTTTGAAACTTAA | 55120 |
| rs577676420 | snp | C/T | 3.44691e-05 | 0.00415131 | intron-variant | FANCL | GRCh38.p7 | 2:58241171 | TTCTCCGCGCAGCTA[C/T]GCTGCAAGAGGCTCT | 55120 |
| rs577698619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233304 | TTCCAAAGTCCCTTA[C/T]TTGCAAAGCCCAGCC | 55120 |
| rs577734361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58214446 | CGTGGTCATAATTCA[A/G]TATTACTATGATCAA | 55120 |
| rs577739284 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58227253 | GTGTGTTACAAGGTG[C/T]TTTTTTAGTTTAGCC | 55120 |
| rs577766967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173222 | CACTCTGCAGGATAT[C/T]ATCCAGGAGAACTTC | 55120 |
| rs577770754 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58208885 | TATCACCTGCATATA[C/G]AGAATCATTAGCCTC | 55120 |
| rs577796907 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58200104 | GTGGTCTACTTCTGG[A/G]AAAAAAAAAAAAGAA | 55120 |
| rs577797259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58173507 | AAAGAAAAGAATTTT[C/T]AACCCAGAATTTCAT | 55120 |
| rs577815723 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243001 | TCTCTGCAGGGGCAG[A/G]ACATAACACCTGCTT | 55120 |
| rs577867469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58220910 | AAATACTATTGATAA[C/T]GGTTAAGAAGTGATA | 55120 |
| rs577884164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208123 | AGGAAATAAATAACT[G/T]TCATTCACTTAAATA | 55120 |
| rs577921303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58220304 | GTCTACATAAAGTCA[C/T]GACTGAAGGAATGGC | 55120 |
| rs577972812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58177449 | TGGAATACTATGCAG[C/G]CATAAAAAAGGATGA | 55120 |
| rs578010985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187129 | ACATATGTTTATTGC[A/G]GCATGATTCACAATA | 55120 |
| rs578048315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58234039 | TACCCAACAGAAGAG[A/G]GTATTCTTAAACTAG | 55120 |
| rs578089612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58177081 | CAAAACCACAACGAG[A/T]TATCATCTCACACCA | 55120 |
| rs578090979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182338 | TGATTCTAATGTGCA[G/T]ATAAGGTTAAAAACC | 55120 |
| rs578136417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193800 | TTGTTTTAAACTCGA[C/T]TTATTTTTCTTTACA | 55120 |
| rs578155567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239592 | ACAAAATTTGAAATA[A/T]GGACTCTATCTTAGA | 55120 |
| rs578166949 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226165 | AATTTGGTCAGGCCC[A/G]GCAGTATTCACTATA | 55120 |
| rs578173683 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58189669 | TTATCTTTAAAAGCA[-/TT]TTGTTACTTTCATAA | 55120 |
| rs578243495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168201 | GTCTGCAGCTCCCAG[C/T]GAGATCAAGGCAGAA | 55120 |
| rs578252754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58168797 | CTGAGGCTTGAGTAC[A/G]TGGTTTACCCCTCAC | 55120 |
| rs745306555 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180842 | TTTGTAATGTGCAAA[C/G]TAATCAAAAAAGAAA | 55120 |
| rs745338794 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240246 | GGATTAACTTTTTTC[C/G]ATATGGAATAATGAA | 55120 |
| rs745366278 | snp | G/T | 0.000300576 | 0.0122555 | intron-variant | FANCL | GRCh38.p7 | 2:58226721 | CAGAAAAAAAAAAAA[G/T]TCTTACCAAAAGCAT | 55120 |
| rs745408295 | snp | A/G | 3.54711e-05 | 0.00421121 | intron-variant | FANCL | GRCh38.p7 | 2:58226819 | ATTAATTTCATTTGC[A/G]CAATAAATATTCTAT | 55120 |
| rs745418634 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58225786 | AGATTTTATAGGACA[A/C]CTAATTTGTTTTATT | 55120 |
| rs745458616 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236860 | AACATTATTACTAAA[C/G]ATAAAAAAGGTCATT | 55120 |
| rs745474533 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58190656 | AAAAGATCATAAAAA[A/C]CTTTACATCACATAA | 55120 |
| rs745516344 | snp | G/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161796 | TCAACATTTACCTTT[G/T]ATGTTGGGAACATTA | 55120 |
| rs745526326 | snp | C/T | 8.23662e-05 | 0.00641688 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165738 | CCTAATGCAATTCTG[C/T]GTGCTGTTGCACTCC | 55120 |
| rs745544496 | snp | C/T | 5.02374e-05 | 0.0050116 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159772 | TTCTTATTTCAGTGT[C/T]TCCTTCCAGACATTT | 55120 |
| rs745549746 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191581 | CATTAATCATCCCTA[C/T]TTCATTTTTGAGCAT | 55120 |
| rs745654892 | snp | A/T | 1.66114e-05 | 0.00288192 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198645 | ATCCACAAAATAATC[A/T]GGTGATTCTGCAGGA | 55120 |
| rs745656000 | in-del | -/TGA | | | intron-variant | FANCL | GRCh38.p7 | 2:58194619 | CCTTGCCCTTGGTGC[-/TGA]TTTCTTACTACTCTA | 55120 |
| rs745713304 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232430 | CCCATAGAAGAAATT[G/T]CAGTGTTATTTCTTA | 55120 |
| rs745726117 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186825 | CTGACTGAAGCAATG[A/T]GGTTGAGTAAAAAGT | 55120 |
| rs745728710 | snp | G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242971 | GTGATTCTGATGCAT[G/T]CTAAGGTTTGAGGAT | 55120 |
| rs745744791 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58225439 | GAATTTTTAAAATTA[A/C]CATTTGTAAATCCTA | 55120 |
| rs745748447 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170274 | AACTAGAATTTCCTA[A/T]CCCGCCAAACTAACC | 55120 |
| rs745754597 | in-del | -/CTCA | 2.02374e-05 | 0.00318092 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161675 | AAAAAGCGTATGTGT[-/CTCA]CTAACTTATTCGTTG | 55120 |
| rs745812922 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58237671 | TCTATCTAGATGTAT[-/C]GGGGGAAAAAATGAG | 55120 |
| rs745816176 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199932 | GTATTTAACAAACAT[G/T]TGAAATCAACACTTT | 55120 |
| rs745819715 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168581 | ACCCCAGTGGCGCCT[A/G]CAACACCAGCAAGAC | 55120 |
| rs745845830 | snp | C/G | 1.66507e-05 | 0.00288532 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162850 | TCTGGAATATCAAAA[C/G]ACTGATAAAACTTAC | 55120 |
| rs745879256 | snp | A/G | 1.68388e-05 | 0.00290158 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163447 | ACCATGGTCAGCTCC[A/G]AGAAAGAAGCACTCA | 55120 |
| rs745923105 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240693 | AAGTTAATTAATTCC[A/G]TTGCTGTCATGCTTC | 55120 |
| rs745987113 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228604 | GCAACAGAGATCTTA[C/T]GGCTTACTAAGCCAG | 55120 |
| rs746005877 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58196088 | ATATAGTAGACAAAC[A/G]TAAGATTATGGCTAA | 55120 |
| rs746046267 | snp | A/C | 1.66134e-05 | 0.00288208 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232080 | CAGTTGTAAATCTTC[A/C]GGCAACACTATCCTA | 55120 |
| rs746057756 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209633 | TTGATACACCTACTT[A/T]ACACTAGGAACTATA | 55120 |
| rs746086230 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58210672 | ATAAAATCAAAAGCA[A/C]GTTAGTTACTTCCTA | 55120 |
| rs746096056 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194842 | AATACATCAAAACAT[C/T]ATCAACCCAGCAGGA | 55120 |
| rs746101341 | snp | A/C | 1.77773e-05 | 0.00298133 | intron-variant | FANCL | GRCh38.p7 | 2:58198537 | TGGATACTCTGGGAC[A/C]ACTGTACTTTTTAAT | 55120 |
| rs746109291 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58233959 | GAGTAAATAAAAAAA[-/C]AACTCCTTCCCACCC | 55120 |
| rs746110289 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58165126 | CATGTTTTGCTTGCT[C/T]ATAATGAAAATACAC | 55120 |
| rs746130633 | in-del | -/A | 6.62257e-05 | 0.005754 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159418 | TAAACAGTTTCCCAC[-/A]AAAAAATCAGCTATA | 55120 |
| rs746200741 | snp | A/T | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204223 | GGTATCCGCATACAC[A/T]AGTCTGGTGAGCAGA | 55120 |
| rs746211577 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231923 | GGAAAAATCAGAAAT[A/G]TTTCTTTTGGGGCAA | 55120 |
| rs746300656 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58173102 | AAAAAGAATAACAAG[A/G]AACGAACAAAGCCTC | 55120 |
| rs746325072 | in-del | -/AATA | 1.78247e-05 | 0.0029853 | intron-variant | FANCL | GRCh38.p7 | 2:58226821 | TAATTTCATTTGCAC[-/AATA]AATATTCTATCCACT | 55120 |
| rs746405545 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184798 | GAACACAATTCTCAG[C/T]AACGTCCTGACCTTA | 55120 |
| rs746454771 | snp | A/G | 1.73219e-05 | 0.0029429 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161631 | ATTCCACAATCCATA[A/G]TAAAATCCTTCAAAA | 55120 |
| rs746489381 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220704 | TGATTTTCTGGTTCT[A/T]TTTAGGTTAGTTATC | 55120 |
| rs746508342 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226768 | AAGCTCATTAGATCA[C/G]GAGAGTGCTGCATTC | 55120 |
| rs746513985 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213297 | CAGTAGCAATTCTAG[C/T]ATGTGGACAGCACAG | 55120 |
| rs746515626 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227060 | CTGTTTCTTGAGCAC[C/T]GTTTACTACTGAATC | 55120 |
| rs746526500 | in-del | -/A | 6.62394e-05 | 0.00575459 | intron-variant | FANCL | GRCh38.p7 | 2:58165879 | TTAAGGAGCTCTGTG[-/A]AAAAAAATGAAAGTT | 55120 |
| rs746574757 | in-del | -/C | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243196 | CAGTATGTTAAACTT[-/C]CCCACCACCACACTT | 55120 |
| rs746577214 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242882 | TCATTCCCTACAGGC[C/T]CCTATTTCAAACCTC | 55120 |
| rs746603917 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58225920 | AACTAAATATAATGT[A/G]AGGACCTTGTTTGCA | 55120 |
| rs746623168 | snp | G/T | 0.000115897 | 0.00761151 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222008 | GGAGGAGGAGGTAGT[G/T]CATACAGCTCTTGTC | 55120 |
| rs746633432 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192865 | AAAAGAAAACAAAAA[C/T]AACAACAACAAAAAA | 55120 |
| rs746676234 | snp | A/G | 1.75001e-05 | 0.002958 | intron-variant | FANCL | GRCh38.p7 | 2:58226688 | AAGAAATCAAGACTT[A/G]CAGTATGGTAACAGT | 55120 |
| rs746678210 | snp | C/T | 1.68298e-05 | 0.00290079 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163473 | ACTCAGGAAGCATAG[C/T]AGGATGCCTGGGGTC | 55120 |
| rs746702765 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184455 | CCACAAATTCTTAAC[A/T]GGAATAGCAAAACAA | 55120 |
| rs746737823 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178518 | CAGAAAAGGCCTTCA[A/G]TAAAATTCAATACCC | 55120 |
| rs746766628 | snp | A/C | 3.32613e-05 | 0.00407793 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232062 | ATATCACCTTGCATT[A/C]TTCAGTTGTAAATCT | 55120 |
| rs746794787 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233934 | AAGTGGGAAACTTAG[A/G]CTCTTATACGAGTAA | 55120 |
| rs746817862 | snp | C/T | 0.000136977 | 0.00827464 | intron-variant | FANCL | GRCh38.p7 | 2:58194293 | ACAAAAGGAATTTCG[C/T]TTTTTTATAATCATA | 55120 |
| rs746855016 | in-del | -/ATA | | | intron-variant | FANCL | GRCh38.p7 | 2:58191674 | TAATTCAATATATAG[-/ATA]ATAATTGCTGTCTGA | 55120 |
| rs746863722 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220549 | AGAAACAAATTTACA[A/T]GGGAACAATTTGGAA | 55120 |
| rs746881377 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201553 | AGCAGAGAAAGAGTG[C/T]CCACCCTCTGATGCA | 55120 |
| rs746890275 | snp | C/T | | | intron-variant, missense | FANCL | GRCh38.p7 | 2:58188676 | AACTGCTGGGCTCAA[C/T]CAATCTTCTCGTCTC | 55120 |
| rs746934437 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169935 | ATGTTTGATTGGTGT[G/T]CCTGAAAGTGATGGG | 55120 |
| rs746936184 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187768 | TGAAAAATCTAGAAC[A/G]TGTGTATACATAAAA | 55120 |
| rs746967598 | snp | G/T | 1.65386e-05 | 0.00287559 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161550 | ATTTGATGGAAAGGT[G/T]GTCCACACTGAGAAT | 55120 |
| rs746986811 | snp | C/G | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198620 | AGGAGGCACAAAATG[C/G]AACAGGAAAATCCAC | 55120 |
| rs747047023 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230101 | ATGACATGCAAACAG[C/T]ACATCTTGTTTTTTA | 55120 |
| rs747077812 | snp | C/G | 4.96463e-05 | 0.00498203 | intron-variant | FANCL | GRCh38.p7 | 2:58204273 | CACCGGGGAGAGCTG[C/G]AGAGGGGAACTGGAG | 55120 |
| rs747082749 | in-del | -/AAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58233695 | GCTAGGAAGGTCAGG[-/AAA]AAAAATGCATGGGAG | 55120 |
| rs747110288 | snp | G/T | 3.30611e-05 | 0.00406565 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159440 | TCAGCTATACACAAT[G/T]CCCAAACTCATTTTA | 55120 |
| rs747143384 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58176472 | GCCCTCAGAAATAAC[A/G]CCGCATATCTACAAC | 55120 |
| rs747159700 | snp | G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241729 | TTGTCCTCTCTCCCT[G/T]AACATACAGAATAAT | 55120 |
| rs747203881 | in-del | -/A | 1.66726e-05 | 0.00288722 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159700 | TTCTCTGAAGATGAT[-/A]ACCAAAATTCCTTTT | 55120 |
| rs747210328 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197584 | AATCATACCACCTTA[C/T]ATCTATGTTATAGTT | 55120 |
| rs747214106 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58196202 | ATATACCAATTTTGG[A/G]TAAACAGTTACTACT | 55120 |
| rs747219246 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184829 | AAAAGTCCCCCAAAA[C/T]GGGAGGAAACATCGT | 55120 |
| rs747253294 | in-del | -/ATA | 0.00051322 | 0.0160108 | cds-indel, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161533 | TTACCTCATATAAGC[-/ATA]TTTGATGGAAAGGTT | 55120 |
| rs747258792 | snp | G/T | 1.67789e-05 | 0.00289641 | intron-variant | FANCL | GRCh38.p7 | 2:58229883 | TAATAATCTAAAATT[G/T]TAATGAGACAAAATG | 55120 |
| rs747285172 | in-del | -/AAGCAAATGGA | | | intron-variant | FANCL | GRCh38.p7 | 2:58170680 | GGAGGAATATTTACC[-/AAGCAAATGGA]AAGCAAAAAAAAAAA | 55120 |
| rs747310464 | in-del | -/TCTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58172713 | AGAAAAACTGGAAAC[-/TCTA]AAAAGCAGAGCGCCT | 55120 |
| rs747348064 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237208 | TATTCACCAGGATAG[A/T]CTATATTATTGGTCA | 55120 |
| rs747354131 | snp | A/G | 1.65573e-05 | 0.00287721 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241267 | GACCGGTTCTGGGGC[A/G]GAAGCAGGGGGCACT | 55120 |
| rs747369292 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214455 | AATTCAGTATTACTA[C/T]GATCAACTACCTAAA | 55120 |
| rs747394195 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163262 | AACTATCATTATTGC[A/G]GTGAACCGAGATCGC | 55120 |
| rs747428014 | snp | A/G | 1.6607e-05 | 0.00288153 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160207 | AAAGATAAAGGAGAA[A/G]CGTCAGCATGATTAC | 55120 |
| rs747432060 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234534 | AAAAAGTCCAGAGTA[C/T]ATATAATTGGAGATC | 55120 |
| rs747432322 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191756 | GAGAGACTACTTCTT[C/T]GCCCATATTAGCTCT | 55120 |
| rs747489023 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172479 | CCACCGCTACTGGTA[C/T]CCAGGCAAACAGGGT | 55120 |
| rs747509910 | snp | A/G | 1.68647e-05 | 0.0029038 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241303 | AACAGGCTCGCTTCC[A/G]TCACCGCCATGGCTC | 55120 |
| rs747520252 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206320 | GAAATATTGCATGTA[A/G]GCAGATTATTTAGAA | 55120 |
| rs747542072 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171940 | GTTTAAAAAACGGCA[C/T]ACCAGGAGATTACAT | 55120 |
| rs747594960 | snp | A/G | 1.66346e-05 | 0.00288393 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160221 | AGCGTCAGCATGATT[A/G]CAAATTACAGATACT | 55120 |
| rs747689832 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58234272 | TCAGACATTTTAAAA[C/G]TAAAATGAGAAATTG | 55120 |
| rs747717121 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202993 | GCCACTGGCAACATG[C/T]GACCCTTTGGAAGGA | 55120 |
| rs747717397 | snp | C/T | | | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161532 | TTTACCTCATATAAG[C/T]ATATTTGATGGAAAG | 55120 |
| rs747746019 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58222496 | ATCCTAACAAACAAA[A/C]TCATTATCAGAACAA | 55120 |
| rs747756237 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214190 | TAGTGAAAAAAGGAG[G/T]CAATTATATTGTGAT | 55120 |
| rs747757276 | in-del | -/C | 0.000136958 | 0.00827408 | intron-variant | FANCL | GRCh38.p7 | 2:58194209 | ACTTCACCAAGCCTG[-/C]CACTTAGTGGCACAC | 55120 |
| rs747759150 | snp | A/G | 1.82121e-05 | 0.00301757 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241336 | AGTCCGGAGAAACAC[A/G]GAAAAGCTCTAGACC | 55120 |
| rs747805067 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215027 | TCAATACAACAGAAA[G/T]AAAACTAGAACATTT | 55120 |
| rs747806073 | in-del | -/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162627 | GGGTAACTGTGGAAC[-/T]TTTAATGTCTGTGGA | 55120 |
| rs747845031 | in-del | -/AA | 0.00119546 | 0.0244192 | intron-variant | FANCL | GRCh38.p7 | 2:58226709 | TGGTAACAGTGTCAG[-/AA]AAAAAAAAAATTCTT | 55120 |
| rs747849105 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166880 | TCATGCTCAGTTCCA[C/T]TGTGCTGGATTCAAC | 55120 |
| rs747892360 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186805 | CAACATACACCACCA[C/G]GAAGCTGACTGAAGC | 55120 |
| rs747900495 | in-del | -/AAG | 3.30371e-05 | 0.00406417 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159493 | AGTCCAGATATATTC[-/AAG]AAGTCAAGATCTCCA | 55120 |
| rs747937355 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222385 | CCATGAATATGATGT[C/T]TGATATATACATTTT | 55120 |
| rs747963330 | snp | A/G | 1.73501e-05 | 0.00294529 | intron-variant | FANCL | GRCh38.p7 | 2:58229775 | ATTTAGTAATTTCTT[A/G]TCTTCACTGAAAACA | 55120 |
| rs747996761 | snp | A/C | 1.65127e-05 | 0.00287334 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159526 | TCTTGGTATAAATAC[A/C]CTTCCACAGTCAGCA | 55120 |
| rs748013648 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179225 | TTAACAGAATTAGAA[A/C]AAAACTACTTTACAT | 55120 |
| rs748023476 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235454 | AGACTAAAGTCTGCT[C/G]TGGGTCTACCTAGCA | 55120 |
| rs748025072 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210869 | ATGCTGATACAAGAG[C/T]TGAGTTCCCATGACC | 55120 |
| rs748025131 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220741 | CCAACTCATAGAAAA[C/T]AGCTAAAAAACAGAT | 55120 |
| rs748066835 | in-del | -/TATG | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188217 | AAACAGCTGTCTGTA[-/TATG]TATGGGTATATTTCT | 55120 |
| rs748118153 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190267 | TTAAAAAATCTGCTA[C/G]TGTTTTTCATTCATG | 55120 |
| rs748118571 | snp | C/T | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165853 | CTGCCAAAAACTGAC[C/T]ATAAATGCTTATTAA | 55120 |
| rs748169090 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58218045 | ACTCAATAACCCAAA[A/C]ATCTCCAGTTGTTTG | 55120 |
| rs748173047 | snp | A/G | 3.3071e-05 | 0.00406625 | intron-variant | FANCL | GRCh38.p7 | 2:58204103 | AAGTATTTTCTGATC[A/G]CAATAACAGTTTAAC | 55120 |
| rs748210226 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229416 | AGTACACATGATCCT[A/T]AATTATTTCTGCCAC | 55120 |
| rs748230800 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58232293 | ATTTGAGGGAAAATA[A/C]CTCAAAACTGTCTTA | 55120 |
| rs748246751 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172582 | AACAGAAAGGACTCT[C/T]AGCTGAGGGTCTGTG | 55120 |
| rs748267861 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172555 | TCTCTGTTAACAGAG[A/G]GTCTGTTTGTTAACA | 55120 |
| rs748285722 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218825 | GGCTACAAAACTACA[C/T]ATGGTAATGGACTGG | 55120 |
| rs748298862 | snp | A/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204207 | TGATGGTACTGAAGC[A/G]GGTATCCGCATACAC | 55120 |
| rs748326873 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231177 | CTTTAAATGTTGGTA[C/T]GCCCCAAGGTCTTGT | 55120 |
| rs748335815 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199562 | AAACCTTTGAAAGAT[A/T]GCTAAATACAAAATT | 55120 |
| rs748425411 | snp | C/G | 1.65578e-05 | 0.00287726 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162978 | AAAAAATTATGCTGT[C/G]AACTTTGTAAAATCA | 55120 |
| rs748435689 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185870 | TTTGGCTTGTACAGT[A/G]TTATTTTCCACTGCT | 55120 |
| rs748444705 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239122 | ATTTGGCAACCGTGA[C/T]AGTAATAGTCGACTC | 55120 |
| rs748507639 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218417 | TGATTAAGAAAAATT[A/T]AAAAGGCACAAAAAA | 55120 |
| rs748526677 | snp | C/G | | | intron-variant, splice-donor-variant | FANCL | GRCh38.p7 | 2:58194228 | TTAGTGGCACACTTA[C/G]AGGCAAAACCGCAAT | 55120 |
| rs748535670 | snp | A/C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226067 | ACAGAGGGATACATA[A/C/T]AATATCCAGAATTTC | 55120 |
| rs748597099 | snp | C/T | 1.67329e-05 | 0.00289243 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159761 | GAAATGTTGTATTCT[C/T]ATTTCAGTGTTTCCT | 55120 |
| rs748619426 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238297 | CAAAGTCTTGGCAAA[C/T]ATCTTGATTGCAAGA | 55120 |
| rs748627103 | snp | C/G | 1.66732e-05 | 0.00288727 | intron-variant | FANCL | GRCh38.p7 | 2:58241206 | GCTAGAAAGCAACCA[C/G]TGGGCGGGTACCTGA | 55120 |
| rs748629241 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164848 | GGAAAGTACCAATAC[G/T]ATTTGTAGAACTGCT | 55120 |
| rs748631020 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237672 | CTATCTAGATGTATC[A/G]GGGGAAAAAATGAGA | 55120 |
| rs748635161 | snp | C/G | 1.65748e-05 | 0.00287874 | intron-variant, downstream-variant-500B, missense, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160085 | AGGCACATTTTATGA[C/G]ATGTGATTAACAATT | 55120 |
| rs748646431 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207736 | AGTGATAAACTCTTA[C/G]AAGTGGTATCAAATC | 55120 |
| rs748678574 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163316 | ACAAGAGCAAAACTC[C/T]GTCTCAGACAAAAAA | 55120 |
| rs748701521 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58193037 | AAAATACTTAAGAAA[A/C]AATTCAACAAAAATA | 55120 |
| rs748767111 | in-del | -/TG | | | intron-variant | FANCL | GRCh38.p7 | 2:58223586 | AGGCAAAAGCAGAGA[-/TG]AGCAACATATTCTTC | 55120 |
| rs748786098 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236658 | TTAAATGTAAATAGT[C/T]GAAGCACCCCCAAGT | 55120 |
| rs748800551 | snp | A/T | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165831 | AATGCCTTTAGTGAT[A/T]CTATTGCTGCCAAAA | 55120 |
| rs748805033 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179990 | TCATCATCACTGGTC[A/T]TTAGAAAAATGCAAA | 55120 |
| rs748806981 | snp | A/C | 3.31934e-05 | 0.00407377 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229851 | CCACTAAGTATTGTT[A/C]TCAGCTGCCAACTAC | 55120 |
| rs748813886 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235593 | CTAGCATGCAACAGG[C/T]AGCATTCATTATGTC | 55120 |
| rs748851619 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203196 | ACATACATATTCTGT[C/G]TGTGAGAGAATTAGT | 55120 |
| rs748867071 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222593 | GTATTATGCCATCCA[A/T]CTGGCTAGATTACAG | 55120 |
| rs748870717 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190330 | AACATAGTCACCTCA[C/T]GTGTAGCCATCACAG | 55120 |
| rs748875030 | snp | C/G | 1.65446e-05 | 0.00287612 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160122 | CCTTACTACAATATG[C/G]ACATTCACCAAATAT | 55120 |
| rs748896681 | in-del | -/AACA | 0.000236546 | 0.0108728 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159315 | GGATAACTCACGTCT[-/AACA]AACTAAACTATATAT | 55120 |
| rs748930217 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216001 | CCCCAGGATCTCTGT[A/G]GGAACTCTTGAAAGA | 55120 |
| rs748960322 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189030 | CAGAATTATATAAGA[C/T]TCTGTAAACTGCAAA | 55120 |
| rs749093931 | snp | G/T | 1.65214e-05 | 0.0028741 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159299 | CACAAAATAAATACT[G/T]GGATAACTCACGTCT | 55120 |
| rs749126716 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223904 | AACATATTTATTGGT[A/G]ATTATAGTATAGGAA | 55120 |
| rs749138542 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212787 | GTCATACCATCTTCA[C/T]GTTAACCTTTGGGGA | 55120 |
| rs749173184 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210932 | TATGGCACCCCCACC[C/T]GGCTGAGTTCATGGG | 55120 |
| rs749191700 | snp | G/T | 1.6557e-05 | 0.00287719 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159413 | ATGAAGTAAACAGTT[G/T]CCCACAAAAAATCAG | 55120 |
| rs749207036 | in-del | -/ACTT | 1.65158e-05 | 0.00287361 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159553 | GCACGGGGATCACAG[-/ACTT]ACTTAGAAAGTTCAA | 55120 |
| rs749222607 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58226496 | CTGCCCAACACTAGT[-/A]GTCAAGAATACCTAG | 55120 |
| rs749224490 | in-del | -/GAGAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58173304 | CACAAAGATACTCTC[-/GAGAA]GAGAAGAGCAACTCC | 55120 |
| rs749228059 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211809 | TAACAAGAGTAACCT[C/T]TGCTCCAGTTCCCAA | 55120 |
| rs749229884 | in-del | -/TTAAG | 3.34124e-05 | 0.00408719 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159724 | CCTTTTGATAATTTT[-/TTAAG]TTAAGTTTCCAGCTC | 55120 |
| rs749253415 | snp | C/T | 0.0145559 | 0.08406 | intron-variant | FANCL | GRCh38.p7 | 2:58226831 | TGCACAATAAATATT[C/T]TATCCACTAAAACTG | 55120 |
| rs749263336 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179967 | CCAACAAACATATGA[A/G]AAAAAGCTCATCATC | 55120 |
| rs749350298 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178575 | TAGGTGTTGATGGAA[-/C]ATATCTCAAAACAGT | 55120 |
| rs749372143 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212355 | TAAATTATCTTCCAC[C/T]GGGTCCCTCCTGCAA | 55120 |
| rs749392186 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58164913 | GTGACATTCTTCCCC[A/C]AGATAATCTATATTA | 55120 |
| rs749405374 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239168 | GACGCTAAAACCAGA[C/G]AATGTGTGTGAAAGT | 55120 |
| rs749411866 | snp | A/C | 3.36185e-05 | 0.00409977 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198662 | GTGATTCTGCAGGAT[A/C]CTATTAAAAAAGCAT | 55120 |
| rs749430436 | snp | C/G | 3.30901e-05 | 0.00406743 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241254 | ATACACGGTTTTCGA[C/G]CGGTTCTGGGGCAGA | 55120 |
| rs749433866 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209360 | TACTGTTAAGCATAT[G/T]ACCAACCTAGAAAAA | 55120 |
| rs749460545 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174702 | CAAAGATCCAAAATT[C/G]ACACCCTGACATCAC | 55120 |
| rs749521594 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207884 | CGACACAGTGAGACC[C/T]CATCTTTACAAAAAT | 55120 |
| rs749523723 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220403 | ACAAAAGGGAAAAAA[G/T]TGATCTACACATAAG | 55120 |
| rs749530493 | snp | A/G | 0.000155379 | 0.0088128 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161663 | AAAAATATTTATAAA[A/G]AGCGTATGTGTCTCA | 55120 |
| rs749543769 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184713 | TGTCTTATAGGAAGA[A/G]AAGTATCCTAGAAAT | 55120 |
| rs749552141 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230045 | TCTTCAAACTGTTGG[C/T]ACTAATTTTATTTCA | 55120 |
| rs749711870 | snp | A/C | 1.68057e-05 | 0.00289872 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163466 | AAGAAGCACTCAGGA[A/C]GCATAGTAGGATGCC | 55120 |
| rs749734256 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220215 | TCTTAAGTACAGATC[A/G]TACACACTTTGACTC | 55120 |
| rs749766976 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194363 | AGTCTCAGTCAAGAG[C/T]ATTTACACATCTGAC | 55120 |
| rs749776730 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58218763 | AGATAATGGGAGCTC[A/G]GTTTCTCCCTGTTGG | 55120 |
| rs749783345 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183027 | GTCAACTTCTTAGAA[G/T]AGAGTAAATGTATAA | 55120 |
| rs749791110 | snp | A/G | 5.60952e-05 | 0.0052957 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163538 | ATGAAACAAGATTAA[A/G]TCTTTTAGAAGTAGA | 55120 |
| rs749811668 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166126 | ATAATTTTTTTATTA[C/T]AATGCTTGATATACT | 55120 |
| rs749841169 | snp | A/T | 1.65531e-05 | 0.00287686 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162957 | GGATCCCTGAAAGCA[A/T]GGGGAAAAAAATTAT | 55120 |
| rs749963743 | snp | A/G | 1.66001e-05 | 0.00288094 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159398 | CTCAAGAACCTTTGA[A/G]TGAAGTAAACAGTTT | 55120 |
| rs749971554 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192746 | AAAGTAGTATAAATA[C/G]AAAAGCATGTAATGA | 55120 |
| rs750013831 | snp | C/T | 3.33244e-05 | 0.0040818 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163041 | TACCACAAATGTATG[C/T]TCCTGCTCAGCTTAA | 55120 |
| rs750038723 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218416 | CTGATTAAGAAAAAT[C/T]AAAAAGGCACAAAAA | 55120 |
| rs750050199 | snp | G/T | 9.99633e-05 | 0.00706907 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163040 | CTACCACAAATGTAT[G/T]TTCCTGCTCAGCTTA | 55120 |
| rs750101616 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172432 | CATCAGACAGCAGCA[C/T]TCGTGGTTCAAGAAA | 55120 |
| rs750109791 | snp | C/T | 1.66056e-05 | 0.00288141 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229830 | TGTTGTACTATTCGA[C/T]GGTATCCACTAAGTA | 55120 |
| rs750192800 | snp | A/G | 3.40368e-05 | 0.00412519 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159835 | TTTAACAAAGTTTGT[A/G]GACACTCTAAAAAAT | 55120 |
| rs750217091 | snp | A/G | 1.65425e-05 | 0.00287593 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241246 | AATCCCTCATACACG[A/G]TTTTCGACCGGTTCT | 55120 |
| rs750243016 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183881 | GTTTGCAAGGAAATC[A/G]CAGCTCTCATATTGA | 55120 |
| rs750244924 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214711 | GACACGGGGTTTCAC[C/G]ATGTTGCCCAGGTTG | 55120 |
| rs750246188 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171397 | TTTCAAGGGAAATTT[A/G]TAACGAAATGCCCAC | 55120 |
| rs750258424 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197096 | AAAGCAAATTACAGG[C/T]TCTCTCTTCTCTATT | 55120 |
| rs750271999 | snp | C/T | 1.78112e-05 | 0.00298417 | intron-variant | FANCL | GRCh38.p7 | 2:58198713 | TCTGTGTGTTAATAT[C/T]ACTGAGGTATTTTAG | 55120 |
| rs750326451 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226860 | TGTAAAAAAATGTAG[A/G]CCCAAGTGAATGTGA | 55120 |
| rs750347352 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181643 | GGTGGAAGAAAGGAT[A/G]AATAAATGGAAAAAC | 55120 |
| rs750348227 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58194871 | GAAGACAGGGACCAT[-/AA]GGAAAATTACCCATT | 55120 |
| rs750377895 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218235 | CTGGAAAAAAATCAA[C/T]GACCTACATATCCAT | 55120 |
| rs750381360 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213935 | AGAATTTATTAAAGG[C/T]TCCATATCGGAGCTG | 55120 |
| rs750429919 | in-del | -/CT | 1.64743e-05 | 0.00287 | intron-variant | FANCL | GRCh38.p7 | 2:58165709 | AACAAACCCTTAATC[-/CT]CTCCTTGTCCCTACC | 55120 |
| rs750486781 | in-del | -/CTC | | | intron-variant | FANCL | GRCh38.p7 | 2:58240708 | ATTGCTGTCATGCTT[-/CTC]CTAGAAGATATTGTA | 55120 |
| rs750490307 | in-del | -/A | 1.66236e-05 | 0.00288297 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159681 | AGTATTTCTTGCTTT[-/A]TTTTTTCTCTGAAGA | 55120 |
| rs750526669 | snp | G/T | 3.31559e-05 | 0.00407147 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226761 | CATCATAAAGCTCAT[G/T]AGATCAGGAGAGTGC | 55120 |
| rs750526887 | in-del | -/AT | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241944 | TATATAAAGCAAAAC[-/AT]GAGTAAAGATTGCTG | 55120 |
| rs750557923 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167381 | CAAGAAGCTAGTTTT[A/G]AAATCAGTACAATAG | 55120 |
| rs750574743 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58211207 | TTCTGAAATCTAGGC[A/G]GAGGTTCTGAAACCT | 55120 |
| rs750588174 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190091 | GTTCATTTGAAGTTA[C/T]TTACAGGCTTCATTG | 55120 |
| rs750596891 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236420 | CGTTAAGGCAGACCA[C/T]GATAGATTTAATATG | 55120 |
| rs750612884 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179835 | AATCTATCCATCTGA[A/C]AAAGGGCTAATATCC | 55120 |
| rs750638810 | snp | A/G | 1.67178e-05 | 0.00289113 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159743 | AGTTTCCAGCTCTTC[A/G]CCGAAATGTTGTATT | 55120 |
| rs750644591 | snp | C/G | 1.64825e-05 | 0.00287071 | intron-variant | FANCL | GRCh38.p7 | 2:58165690 | TACAAAATAAAACAC[C/G]TAAAAACAAACCCTT | 55120 |
| rs750688887 | snp | A/C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191120 | TTCCAAATTAGCCCC[A/C/T]GGATTATAAAAAAAA | 55120 |
| rs750748716 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230857 | TTTTCTCCTTAATGA[A/G]TTAACTTGCTCAAAT | 55120 |
| rs750759235 | snp | A/G | 1.65482e-05 | 0.00287643 | stop-gained, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198596 | GAGGAGAATTTACCT[A/G]AGGTGTCCAGGAGGC | 55120 |
| rs750794812 | snp | A/G | | | | | GRCh38.p7 | 2:58243407 | TACCATAAACTGGAT[A/G]GGTAATCCGCAGAAA | 55120 |
| rs750819881 | snp | A/C | 3.31785e-05 | 0.00407286 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161591 | TTGATCAGGAATGGT[A/C]CCGTCAAGTTGATAA | 55120 |
| rs750837379 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217642 | AACCAACAAGGAAGA[C/T]ATAGCAATTATAAAT | 55120 |
| rs750850383 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231795 | TTCAGTATTTGTTAG[A/T]GAAGTGTACACAATG | 55120 |
| rs750864824 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58169612 | AACTCCTCTGAGCTA[A/C]AGGAGCATGTTCTAA | 55120 |
| rs750865052 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212318 | ACCATGAGAACAGTA[C/T]GGGGGAAACTGCCCC | 55120 |
| rs750871999 | in-del | -/CT | 0.00011581 | 0.00760864 | frameshift-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160147 | AATATGATGTTAAAA[-/CT]CTCTGTCTACTAGTT | 55120 |
| rs750882229 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168981 | AAACTCCCATCTCCC[C/T]GGGACAGAGCACGTG | 55120 |
| rs750883890 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186426 | AAGGACATGTATGGG[G/T]AAAATTTATTGGAAG | 55120 |
| rs750918226 | snp | C/G | 1.65176e-05 | 0.00287376 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221976 | CTATCTCTTCAATAA[C/G]GCTTGAGTAGAACTG | 55120 |
| rs750930860 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197364 | CTAACCAAAATTTTA[C/T]AGCCAAAATGAGTAG | 55120 |
| rs750989355 | snp | C/G/T | 5.21176e-05 | 0.00510456 | intron-variant | FANCL | GRCh38.p7 | 2:58198702 | CCATTTTTGCTTCTG[C/G/T]GTGTTAATATCACTG | 55120 |
| rs750994405 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190332 | CATAGTCACCTCATG[C/T]GTAGCCATCACAGAG | 55120 |
| rs750998663 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168340 | CCTCACTCAGGAAGC[A/G]CAAGGGGTTGGGGAG | 55120 |
| rs751025755 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240032 | TTCTAATGGGTGTAC[C/T]TGTTTCCTAAAAGGC | 55120 |
| rs751083138 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188428 | TAATTCTCTTAATTT[C/T]GGGGTTTTTTTGTTT | 55120 |
| rs751096663 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58182722 | AAAATTAAGTAAACA[A/C]ATATTACATAAATGA | 55120 |
| rs751140292 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228123 | TAATTGTGATTTTTG[-/T]TCCTCTCACAACTAA | 55120 |
| rs751175000 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213365 | CAATTTTATCAGTGT[A/G]TGTGTGTACCAGACC | 55120 |
| rs751221353 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58233231 | AATTCTTAATTTACA[A/C]GAAAAATAGAAGAAC | 55120 |
| rs751234269 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210192 | CATGCTGCTAAGACA[C/T]ACCCAAGACTTGGCA | 55120 |
| rs751234408 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58194134 | ATGATAAAAAAATAT[A/G]AAGACCACTATTTAC | 55120 |
| rs751258176 | snp | C/T | 0.000115673 | 0.00760415 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159633 | CGCAGATGTTTATTA[C/T]TATCGCATCATCATA | 55120 |
| rs751264572 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178825 | CATGACTGTATATTT[A/T]CAAAACCCTATCATC | 55120 |
| rs751346195 | snp | A/G | 1.79053e-05 | 0.00299204 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163521 | AAACATTATTACCTA[A/G]AATGAAACAAGATTA | 55120 |
| rs751386006 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174113 | ATATATGCACCCAAT[A/G]CAGGAGCACCCAGAT | 55120 |
| rs751391869 | snp | C/T | 0.000102907 | 0.00717238 | intron-variant | FANCL | GRCh38.p7 | 2:58232150 | TCACTCAAATTTTTA[C/T]CTTTCACTTAATGCT | 55120 |
| rs751395531 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161153 | ATTTCATTTTCACTG[C/T]ATTACTGCCACTTTC | 55120 |
| rs751396703 | in-del | -/A | 1.83117e-05 | 0.00302581 | intron-variant | FANCL | GRCh38.p7 | 2:58222090 | GAACGCAAGACAATG[-/A]AACTGTTAATACCTG | 55120 |
| rs751435009 | snp | C/T | 1.67049e-05 | 0.00289002 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159723 | TTCCTTTTGATAATT[C/T]TTTAAGTTTCCAGCT | 55120 |
| rs751457434 | in-del | -/GGTG | | | intron-variant | FANCL | GRCh38.p7 | 2:58198037 | TGGATGGTGTGTGTG[-/GGTG]TGTGTGTGCGTGTGT | 55120 |
| rs751505799 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214840 | TAAGTCTTGCCTTAT[A/G]TATCCTTAGTGCTTT | 55120 |
| rs751506003 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58228921 | TCAACAGATGCATTT[C/G]TTAAATTTTAGTGTA | 55120 |
| rs751529162 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202845 | ACATCTTCTTAGGAA[A/G]TAGAAGAGCTTGTAA | 55120 |
| rs751529494 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184235 | ATATACAATAACAAT[G/T]TACTCTTTGATCAAA | 55120 |
| rs751618033 | in-del | -/AAAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58165694 | AAATAAAACACCTAA[-/AAAC]AAACCCTTAATCCTC | 55120 |
| rs751623466 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219618 | GTCACAGAGATAACA[C/T]GTACCCTTGATATGA | 55120 |
| rs751642410 | in-del | -/T | 1.80122e-05 | 0.00300096 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163109 | AATTTAATAATTGCA[-/T]GCTCTACTCTTGGTT | 55120 |
| rs751652562 | snp | A/C | 3.90351e-05 | 0.00441769 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241351 | AGAAAAGCTCTAGAC[A/C]TGCTGGGTCCTGCAC | 55120 |
| rs751713797 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169008 | CGTGGGGAAAGGGGC[A/G]GCTGTGGGCACAGCT | 55120 |
| rs751725062 | snp | A/G | | | | | GRCh38.p7 | 2:58243469 | GTCCAAAATCAAGAC[A/G]CAAGGACAAGATTTG | 55120 |
| rs751735308 | snp | C/T | 1.6537e-05 | 0.00287545 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221964 | AACCAAGAGTTCCTA[C/T]CTCTTCAATAAGGCT | 55120 |
| rs751738439 | in-del | -/AAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58218375 | TCTTTGAAAAAACTT[-/AAA]TAATTGATATGGCTC | 55120 |
| rs751767432 | in-del | -/A | 1.66352e-05 | 0.00288398 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161489 | ATGTTGTGTTAGCGG[-/A]AAAAAAGTCTTGACA | 55120 |
| rs751775155 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163935 | GGCCAAATGTAAAAA[A/G]ACCAACAATACAGTA | 55120 |
| rs751805275 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239865 | AATTACTTGTACTGT[A/G]TATCCTTGCTACTTT | 55120 |
| rs751815103 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58192175 | TTTGGGTCTTTAAAT[G/T]CATGAGAGAGCTTTG | 55120 |
| rs751857451 | snp | A/G | 1.71525e-05 | 0.00292847 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163424 | AACGTTTAAATCTCA[A/G]ATGTCATACCATGGT | 55120 |
| rs751865450 | snp | A/G/T | 5.26869e-05 | 0.00513236 | intron-variant | FANCL | GRCh38.p7 | 2:58222069 | AAGAAAACCTGAATT[A/G/T]GCTGTGGAACGCAAG | 55120 |
| rs751889330 | snp | A/C | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165813 | TCATCCATAACATCC[A/C]AGAATGCCTTTAGTG | 55120 |
| rs751931283 | snp | A/G | 1.66554e-05 | 0.00288573 | intron-variant | FANCL | GRCh38.p7 | 2:58165906 | AGTTGAATAAGTTAT[A/G]TGGTACTCTACCAAT | 55120 |
| rs751939371 | in-del | -/ATAGTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58218124 | TAATATTTTTAACTG[-/ATAGTA]ATAGAAATATAACAT | 55120 |
| rs751966007 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232038 | AATGCACGTTTATAA[C/T]TAAACACCATATCAC | 55120 |
| rs751986875 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200694 | ATTCAAGTAGGATTC[A/G]GTATAGTAAATGGTA | 55120 |
| rs752015879 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220156 | TTAACAGTTGAAATC[C/T]GAGGCTGTAATTTTT | 55120 |
| rs752026540 | snp | A/G | 8.30503e-05 | 0.00644346 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161505 | AAAAAAGTCTTGACA[A/G]TATTTTTATTTTTTA | 55120 |
| rs752072108 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204621 | AGTATGAGACTTTAA[C/T]GCTCCCTTTGTTTTT | 55120 |
| rs752115874 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58233332 | GCCATTTTAAAAGGT[A/C]AAATAACATGTCACA | 55120 |
| rs752155510 | snp | C/G | 0.000116888 | 0.00764397 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159711 | ATGATACCAAAATTC[C/G]TTTTGATAATTTTTT | 55120 |
| rs752203283 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215932 | AAGTTCATAATACAA[A/G]GAGAAATTAATTGGA | 55120 |
| rs752265733 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58185125 | AAATATTCCCTGATA[C/T]GGAATCTAATCTTCC | 55120 |
| rs752293058 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229157 | CTGCCTTTAAGACAC[A/G]GAAATATAGAAAATC | 55120 |
| rs752302198 | snp | C/G/T | 1.66882e-05 | 0.00288857 | intron-variant | FANCL | GRCh38.p7 | 2:58241204 | TAGCTAGAAAGCAAC[C/G/T]ACTGGGCGGGTACCT | 55120 |
| rs752306135 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230578 | AGTAACTCTTCTAAG[C/G]AATTACTTTTAGTTA | 55120 |
| rs752366828 | snp | A/C | 1.75053e-05 | 0.00295844 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163090 | CTTCAGATTAAAAAA[A/C]AAAAATTTAATAATT | 55120 |
| rs752369559 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58195647 | CAGAGATATTTATAT[A/C]CCATATAACTAACAA | 55120 |
| rs752399043 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167129 | AGGCAGGAGAATCAC[C/T]TGAACCCGGGAGGCA | 55120 |
| rs752429763 | snp | A/G | 1.71858e-05 | 0.00293132 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161628 | CAAATTCCACAATCC[A/G]TAGTAAAATCCTTCA | 55120 |
| rs752432769 | snp | A/G | | | intron-variant, missense | FANCL | GRCh38.p7 | 2:58188679 | TGCTGGGCTCAATCA[A/G]TCTTCTCGTCTCGGC | 55120 |
| rs752435993 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58191127 | TAGCCCCTGGATTAT[-/A]AAAAAAAAAAATTCA | 55120 |
| rs752469482 | snp | C/T | 1.66543e-05 | 0.00288563 | stop-gained, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221948 | CAGACATACTTATCC[C/T]AACCAAGAGTTCCTA | 55120 |
| rs752487532 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237733 | AAAGCTATTTTTAAC[G/T]TATATCCATAAATTA | 55120 |
| rs752522785 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213631 | TTAATCCCAGCATTT[C/T]GGGAGGCTGAGGCAG | 55120 |
| rs752527589 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235536 | AAGTAATTTAACTGT[A/G]GCTCACAACAAATCT | 55120 |
| rs752602996 | snp | C/T | 3.30229e-05 | 0.0040633 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159587 | GACTTTGGCCTACAA[C/T]TTCCCAGTTTACTCT | 55120 |
| rs752611534 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58233314 | CCTTATTTGCAAAGC[A/C]CAGCCATTTTAAAAG | 55120 |
| rs752633179 | snp | A/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161466 | GTATTTCAAACAGGA[A/T]TACTTCCTATGTTGT | 55120 |
| rs752636820 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174518 | TACATGGAAACTGAA[C/G]AACCTGCTCCAGAAT | 55120 |
| rs752637829 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171783 | GCAGTGCACCATGCG[C/T]GAGCAGAAGCAGGAC | 55120 |
| rs752645285 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216860 | AGCACGGGGGTAAAG[C/T]GGGTGAGGAGAAGAG | 55120 |
| rs752653495 | in-del | -/ACAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58178457 | AACGTAACCCATCAC[-/ACAA]ACAGAACCAAAAACA | 55120 |
| rs752703285 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202594 | TTTTGCAAGAATATC[C/T]ATAAAAGTGCTTCGT | 55120 |
| rs752784771 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199297 | TCTCTGTTTATCTTT[A/T]AAATAAGAGATCAAA | 55120 |
| rs752844204 | snp | A/C | 1.66175e-05 | 0.00288244 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161502 | CGGAAAAAAGTCTTG[A/C]CAATATTTTTATTTT | 55120 |
| rs752861007 | snp | A/G | 1.75931e-05 | 0.00296584 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241322 | CCGCCATGGCTCGAA[A/G]TCCGGAGAAACACAG | 55120 |
| rs752869374 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233631 | AAAAATATGAAGCAC[C/T]TTCCAATAGAACCTA | 55120 |
| rs752872804 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221432 | TTTCTTTATGCATCA[A/G]TTTTAAAAAAAAAAT | 55120 |
| rs752877891 | in-del | -/C | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158926 | ACTGTACAGTGGACA[-/C]CTTCTCAGTTGCCAT | 55120 |
| rs752884189 | snp | A/G | 0.000198364 | 0.00995703 | intron-variant | FANCL | GRCh38.p7 | 2:58204262 | AAAAATGATCACACC[A/G]GGGAGAGCTGGAGAG | 55120 |
| rs752905815 | in-del | -/TT | 0.000130299 | 0.00807048 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163400 | AGGATTTTATGACTC[-/TT]TATTAAAAAACGTTT | 55120 |
| rs752934177 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201056 | TCATAAATATTAAAA[C/T]ATAAACTAGCATACT | 55120 |
| rs752937872 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214603 | AGCCTCGACCTACCC[A/G]GGCTCAAGTGATCCT | 55120 |
| rs753054636 | snp | C/T | 3.42683e-05 | 0.0041392 | intron-variant | FANCL | GRCh38.p7 | 2:58226796 | TTCTCTAGATCAAAA[C/T]ATTTCCAATTAATTT | 55120 |
| rs753065395 | snp | A/G | 3.33084e-05 | 0.00408082 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159389 | ATCAAGAGTCTCAAG[A/G]ACCTTTGAATGAAGT | 55120 |
| rs753094121 | in-del | -/TAT | 1.79486e-05 | 0.00299566 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159334 | ACTAAACTATATATG[-/TAT]TATTTTTTCCATAGG | 55120 |
| rs753105795 | snp | C/G | 1.66391e-05 | 0.00288431 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229819 | AAGGACTTACCTGTT[C/G]TACTATTCGATGGTA | 55120 |
| rs753107654 | snp | C/T | 1.64738e-05 | 0.00286995 | splice-donor-variant | FANCL | GRCh38.p7 | 2:58165723 | TCCTCCTTGTCCCTA[C/T]CTAATGCAATTCTGC | 55120 |
| rs753112210 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185508 | AGGTCACCAAATCAC[A/G]AACTTACAAAAAAAC | 55120 |
| rs753127092 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188416 | TACATTTTGGAATAA[C/T]TCTCTTAATTTCGGG | 55120 |
| rs753147862 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210468 | TTCAAGATGAGACTT[-/G]GGTAGGGACACAGAG | 55120 |
| rs753157858 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209171 | TTTTAGCTTGCCAAA[C/T]ACATAATAAACTTTT | 55120 |
| rs753158508 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179630 | CTAAAACCATAAAAA[C/G]CCTAGAAGAAAACCT | 55120 |
| rs753167651 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166008 | GACTCCAGTAAACAG[C/T]AGTCGACTCTCCCTG | 55120 |
| rs753212374 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220337 | ACCTATCTCTGCACA[C/T]AGGTGCACCAAAAGA | 55120 |
| rs753212697 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234820 | GCAAGAATGAAATAG[A/T]AAATGTTAAGAAACT | 55120 |
| rs753218842 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58183328 | AGTTACAGGATGGTG[-/A]AAAAAAAAATTAAGT | 55120 |
| rs753232320 | snp | C/T | 4.94246e-05 | 0.0049709 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165798 | GTCTTCTCATCGATT[C/T]CATCCATAACATCCC | 55120 |
| rs753283095 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207980 | AGAAGGTTTGCTTGA[A/G]CTGAAAAGTTTGAGG | 55120 |
| rs753295594 | snp | C/T | 1.65151e-05 | 0.00287355 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159513 | GTCAAGATCTCCATC[C/T]TGGTATAAATACACT | 55120 |
| rs753353983 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205553 | GATTCAAGATGTTAA[C/G]CACATGCATTTATAT | 55120 |
| rs753361995 | in-del | -/CTGCAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58227087 | ATCCCTTGTCCCCCT[-/CTGCAA]TGCAGGGCATGCGAT | 55120 |
| rs753400574 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172263 | TGGTTCTCTCAGCAC[A/G]CACCTGGAGATCTGA | 55120 |
| rs753412993 | snp | C/T | 1.65132e-05 | 0.00287339 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159581 | CAACTGGACTTTGGC[C/T]TACAATTTCCCAGTT | 55120 |
| rs753448913 | snp | A/T | 3.3695e-05 | 0.00410443 | intron-variant | FANCL | GRCh38.p7 | 2:58232032 | TGCAAAAATGCACGT[A/T]TATAACTAAACACCA | 55120 |
| rs753449397 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230784 | CCTGCTACCAACTTG[A/G]TGACTTCAATTAATT | 55120 |
| rs753453584 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171857 | TCTTTCCTAGTCAAA[C/G]AAAGGGGTGACAGAC | 55120 |
| rs753522452 | snp | C/T | 0.000105595 | 0.00726541 | intron-variant | FANCL | GRCh38.p7 | 2:58198549 | GACAACTGTACTTTT[C/T]AATTACTTAAAACAA | 55120 |
| rs753546868 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58185313 | CCTAAATCAGAAATA[A/C]CCTGACTGTTCCGTA | 55120 |
| rs753559993 | snp | A/G | 1.69135e-05 | 0.002908 | intron-variant | FANCL | GRCh38.p7 | 2:58165926 | ACTCTACCAATAGCA[A/G]ATAATCTTTTACTTA | 55120 |
| rs753605014 | snp | C/G | 1.74339e-05 | 0.0029524 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241318 | GTCACCGCCATGGCT[C/G]GAAGTCCGGAGAAAC | 55120 |
| rs753632420 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226619 | AAAACATCAAATGAC[C/T]GAGAGTTAAGAAGAC | 55120 |
| rs753659121 | in-del | -/GTT | 1.65403e-05 | 0.00287574 | cds-indel, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161548 | ATATTTGATGGAAAG[-/GTT]GTCCACACTGAGAAT | 55120 |
| rs753690162 | snp | C/T | 1.65504e-05 | 0.00287662 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162969 | GCATGGGGAAAAAAA[C/T]TATGCTGTGAACTTT | 55120 |
| rs753725513 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238763 | AAAAAGGACCTTCCA[C/T]GAGAAAATTTTTACA | 55120 |
| rs753726472 | snp | A/C | 6.60153e-05 | 0.00574485 | intron-variant | FANCL | GRCh38.p7 | 2:58204249 | GCAGAGGAGAATAAA[A/C]AATGATCACACCGGG | 55120 |
| rs753743452 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160322 | TGCAAGAGTAAGGGA[C/T]GTATTTCCTGAGCCA | 55120 |
| rs753744833 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58238548 | CCTAGATGAAACTAA[A/C]AAATTCCTTGAAAGA | 55120 |
| rs753745302 | snp | A/T | 1.72436e-05 | 0.00293624 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163082 | TTTTACCACTTCAGA[A/T]TAAAAAAAAAAAATT | 55120 |
| rs753748561 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58181495 | CACTTAAGATTTATG[A/C]ACTTTACTGTTTCCA | 55120 |
| rs753763139 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237809 | TTGAATATAGACTAA[A/G]AAACTTGCATCTAAC | 55120 |
| rs753779903 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207114 | TTTGGCCAGTGGACT[A/G]CAAGCACAAGTGATG | 55120 |
| rs753817524 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225413 | TTTTCAACTAATAAA[C/T]GCAGATGATGGAATT | 55120 |
| rs753849862 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189935 | ATAATCCTTTTTTTT[C/T]CTTTATCTTTGGGGG | 55120 |
| rs753873754 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58236247 | AAAAGCAGCCAGAGG[-/A]AAAAAAATATTCTAT | 55120 |
| rs753914335 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58236196 | GGTACAACACACATC[A/C]AAGTGACTGAAACCA | 55120 |
| rs753922391 | snp | G/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165789 | AGTACCCAGGTCTTC[G/T]CATCGATTTCATCCA | 55120 |
| rs753957462 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233800 | AAAGAGAAGACTTAA[C/T]GTGCATTAACACAAA | 55120 |
| rs753977997 | snp | A/T | 1.65545e-05 | 0.00287697 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160168 | TCTACTAGTTAGTAG[A/T]CCTCTCAGCCACTGC | 55120 |
| rs754028115 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221997 | AGTAGAACTGGGGAG[A/G]AGGAGGTAGTGCATA | 55120 |
| rs754060283 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200298 | GCTTTCTTTGGTTCC[A/G]GCTCTGCTAACTAAG | 55120 |
| rs754094663 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235167 | CAGGAGAGAAATGCA[C/T]GGAGAGTAGAGAAAT | 55120 |
| rs754141546 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223930 | AGGAACCCTATTACT[A/T]ACAATACAGCCTAAC | 55120 |
| rs754164758 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168174 | CAAGATGGCCAAACA[A/G]GAACAGCTCCAGTCT | 55120 |
| rs754247473 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229482 | TTTTTGCCACAGATA[C/T]CCCACAGCTCTAAAT | 55120 |
| rs754251274 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242352 | GGTTCTCAAAACGTG[A/G]TCCTAGAACCTAGCA | 55120 |
| rs754251607 | snp | A/G | 1.83117e-05 | 0.00302581 | intron-variant | FANCL | GRCh38.p7 | 2:58222090 | GGAACGCAAGACAAT[A/G]AACTGTTAATACCTG | 55120 |
| rs754317128 | in-del | -/AAAC | 3.31532e-05 | 0.0040713 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159404 | ACCTTTGAATGAAGT[-/AAAC]AAACAGTTTCCCACA | 55120 |
| rs754317980 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195836 | CTTATACAACAATCT[A/T]GGGAAGGCAATTTGT | 55120 |
| rs754327369 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58166376 | AATTAGGCAGAGTAT[A/G]AAAAGGTTTTACACA | 55120 |
| rs754336239 | in-del | -/GTTA | 1.65721e-05 | 0.0028785 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159663 | ACCTGTCCTTTTGAT[-/GTTA]GTATTTCTTGCTTTA | 55120 |
| rs754355543 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179698 | TTCATGACTAAAACA[A/C]CAAAAGCAATGGCAA | 55120 |
| rs754363315 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210575 | GCCCCCCAAAGTCTT[A/T]ACTTATTTCATCATT | 55120 |
| rs754363760 | snp | C/T | 1.66671e-05 | 0.00288674 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226777 | AGATCAGGAGAGTGC[C/T]GCATTCTCTAGATCA | 55120 |
| rs754384095 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213096 | CAGATTTTATGATTA[C/T]ACTGACAAATCTACA | 55120 |
| rs754404240 | in-del | -/AG | | | intron-variant | FANCL | GRCh38.p7 | 2:58235689 | TGAAGAGAAAAATCA[-/AG]AGAGACATAAAAATG | 55120 |
| rs754412490 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211108 | CCCACACTTCCCTTC[C/T]GCATTGTCCTAACAG | 55120 |
| rs754437507 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184330 | CTTTATATCTCCATG[G/T]ATTTAAAGGAGAAGT | 55120 |
| rs754464286 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169944 | TGGTGTGCCTGAAAG[A/T]GATGGGGAGAGTGGA | 55120 |
| rs754478291 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195618 | AAATATATACAAAGT[G/T]AAAAGACATGCCACA | 55120 |
| rs754490341 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182828 | TGGTGATACTAACAA[C/T]ATAGAAGATGCAATA | 55120 |
| rs754498146 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222359 | CTCAAGGCTTCACTA[C/T]GGCTCTATTCCCATG | 55120 |
| rs754508256 | snp | C/T | 1.68312e-05 | 0.00290092 | intron-variant | FANCL | GRCh38.p7 | 2:58232033 | GCAAAAATGCACGTT[C/T]ATAACTAAACACCAT | 55120 |
| rs754547551 | in-del | -/T | 3.48699e-05 | 0.00417537 | intron-variant | FANCL | GRCh38.p7 | 2:58226696 | AGACTTGCAGTATGG[-/T]TAACAGTGTCAGAAA | 55120 |
| rs754628864 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58188771 | CTTAAATTAGGAAGG[-/A]AAAAAAAAAAAAGAG | 55120 |
| rs754630887 | snp | A/G | 0.000137071 | 0.00827748 | intron-variant | FANCL | GRCh38.p7 | 2:58194184 | GGATTCCAACTGCCC[A/G]TGGCAAGAATACTTC | 55120 |
| rs754662879 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199288 | CAAACTGGATCTCTG[-/T]TTATCTTTAAAATAA | 55120 |
| rs754697786 | snp | C/T | 0.000115596 | 0.00760164 | intron-variant | FANCL | GRCh38.p7 | 2:58204255 | GAGAATAAAAAATGA[C/T]CACACCGGGGAGAGC | 55120 |
| rs754713515 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240059 | AGGCCTTAGCAGATA[C/T]AGACATACATAACAG | 55120 |
| rs754716488 | snp | C/G | | | intron-variant, stop-gained | FANCL | GRCh38.p7 | 2:58188700 | TCGTCTCGGCCTCCT[C/G]AAGTGTTGGGATTAC | 55120 |
| rs754730197 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235262 | CTTGCTCCATGGATA[C/T]GAGGAAAACACCCAA | 55120 |
| rs754739168 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58227190 | GAGCTCCAACCCCAC[A/C]GCAGTGTCTAGGGGT | 55120 |
| rs754804945 | snp | A/G | 6.62394e-05 | 0.00575459 | intron-variant | FANCL | GRCh38.p7 | 2:58204087 | CAGAGTTCATTTCAC[A/G]AAGTATTTTCTGATC | 55120 |
| rs754806566 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202881 | AGGACAGGGTGTATT[C/T]AAAATCTTTAGTTTT | 55120 |
| rs754829173 | in-del | -/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241431 | TGGCGGGAAGATCCT[-/G]GAGGATTCCGCGGGC | 55120 |
| rs754842029 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58190133 | TCTTTCTACAGGTAT[A/C]TCTGTAACTGAATTT | 55120 |
| rs754860957 | snp | A/T | 3.81134e-05 | 0.00436523 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163084 | TTACCACTTCAGATT[A/T]AAAAAAAAAAATTTA | 55120 |
| rs754861669 | snp | C/G | 1.67525e-05 | 0.00289413 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159775 | TTATTTCAGTGTTTC[C/G]TTCCAGACATTTTTA | 55120 |
| rs754868989 | snp | A/C | 1.65573e-05 | 0.00287721 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159418 | GTAAACAGTTTCCCA[A/C]AAAAAATCAGCTATA | 55120 |
| rs754894485 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215890 | ATAAAAAGTCAAGCA[A/G]AAAGGCAATGAAAAA | 55120 |
| rs754912741 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170582 | ACTGGCAAATTGGAT[A/G]AACAGTGAAGACCCA | 55120 |
| rs754967702 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172501 | AAACAGGGTCTGGAG[C/T]GGACCTCTAGCAAAC | 55120 |
| rs755028404 | snp | A/G | 1.6615e-05 | 0.00288223 | stop-gained, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229858 | GTATTGTTCTCAGCT[A/G]CCAACTACATAATAA | 55120 |
| rs755044475 | snp | A/C/T | 3.30908e-05 | 0.00406749 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241255 | TACACGGTTTTCGAC[A/C/T]GGTTCTGGGGCAGAA | 55120 |
| rs755065491 | snp | A/G | | | | | GRCh38.p7 | 2:58243574 | GATACACTGGACAGT[A/G]TGACCACTTGCCAAA | 55120 |
| rs755079242 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194972 | GTTTAAAGTCCAGAA[A/T]CACTGACTCCAAAGA | 55120 |
| rs755108270 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159869 | ATTGCTTTGTACTAG[A/G]AATAGTGTCATAGAA | 55120 |
| rs755125058 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200914 | CTTTACTTCATATCT[C/G]AGTTAAATGAGTATT | 55120 |
| rs755144777 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169016 | AAGGGGCGGCTGTGG[C/G]CACAGCTTCAGCAGA | 55120 |
| rs755189717 | snp | A/G | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164115 | AAGTAACCTAATTTC[A/G]CAAGACCTAAGAAAA | 55120 |
| rs755199779 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181427 | ATGTTAATAATGTTC[C/T]GCATCTTGACTGTGG | 55120 |
| rs755202899 | in-del | -/TTA | 1.66087e-05 | 0.00288168 | intron-variant, cds-indel, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161511 | GTCTTGACAATATTT[-/TTA]TTTTTTACCTCATAT | 55120 |
| rs755203374 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241895 | TTAGACTCAAGTCAA[C/T]ACTGGACTCAGTTCT | 55120 |
| rs755272184 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168473 | AGGAGATTCCCTCTG[A/G]TGCCTATTTCACCAG | 55120 |
| rs755328491 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208833 | AATACATTTTTAATC[A/G]TATCAATCCCTTGCT | 55120 |
| rs755349971 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207653 | AATAGAGACTATTTG[C/T]ATCAATTTATGACAG | 55120 |
| rs755374298 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183011 | ATAATGAAGATAAAA[C/T]GTCAACTTCTTAGAA | 55120 |
| rs755417959 | snp | C/T | 1.68221e-05 | 0.00290014 | splice-acceptor-variant, intron-variant | FANCL | GRCh38.p7 | 2:58226786 | GAGTGCTGCATTCTC[C/T]AGATCAAAATATTTC | 55120 |
| rs755447831 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207244 | AGCTAGCAAAGATCA[C/T]GAGGACAGGAACAAC | 55120 |
| rs755464452 | snp | A/C/G | 3.76628e-05 | 0.00433939 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163540 | GAAACAAGATTAAAT[A/C/G]TTTTAGAAGTAGAAC | 55120 |
| rs755477979 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206558 | CATTGTTGCTCACCA[C/T]CACAATGTTTAAAAT | 55120 |
| rs755502639 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant | FANCL | GRCh38.p7 | 2:58165703 | ACCTAAAAACAAACC[A/C]TTAATCCTCCTTGTC | 55120 |
| rs755566712 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171808 | CAGGACGAGGCACTG[C/T]CTCCCTCGGGAAGTG | 55120 |
| rs755611049 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217026 | GAATAAGGAATTGCA[G/T]ACTCTGTATGACTGA | 55120 |
| rs755618937 | snp | A/G | 1.65162e-05 | 0.00287365 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159504 | ATTCAAGAAGTCAAG[A/G]TCTCCATCTTGGTAT | 55120 |
| rs755624278 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215963 | ATTCAGGGCCTACCA[A/G]TGAGACAAAGTCTCA | 55120 |
| rs755632860 | snp | A/G | 1.65712e-05 | 0.00287843 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159405 | ACCTTTGAATGAAGT[A/G]AACAGTTTCCCACAA | 55120 |
| rs755677747 | snp | A/T | 0.000180193 | 0.00949021 | intron-variant | FANCL | GRCh38.p7 | 2:58226823 | ATTTCATTTGCACAA[A/T]AAATATTCTATCCAC | 55120 |
| rs755689605 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224773 | ATACTACAATGATGT[C/T]AACATTAGAAAACAG | 55120 |
| rs755715438 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204422 | AGCCTAGCACTTAAT[A/G]CAGTCATATATCTCT | 55120 |
| rs755748731 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58226709 | TGGTAACAGTGTCAG[-/A]AAAAAAAAAAATTCT | 55120 |
| rs755763054 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185207 | GGAAAAAATAGACAT[C/G]TCCACATCATTTGAA | 55120 |
| rs755783905 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206327 | TGCATGTAGGCAGAT[-/T]ATTTAGAAACATGGA | 55120 |
| rs755786403 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215084 | CATTTCCAACTATGC[G/T]CTAAAAAACAAATAT | 55120 |
| rs755792621 | snp | C/G | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165821 | AACATCCCAGAATGC[C/G]TTTAGTGATTCTATT | 55120 |
| rs755816246 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184586 | CATACAATAATAAGA[A/G]TAAGGAAATGAATAA | 55120 |
| rs755831120 | in-del | -/TGTG | | | intron-variant | FANCL | GRCh38.p7 | 2:58227664 | CAACGTCCAGCCACT[-/TGTG]TGTGTGTGTGCCTGC | 55120 |
| rs755860411 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229226 | AGGCAATTCTAAAAA[C/T]TATTTTTCTAAAAGA | 55120 |
| rs755868073 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179943 | TCTCAAAAGAACACA[G/T]TTATGCGGCCAACAA | 55120 |
| rs755869574 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223782 | CACTTGTTAAATATA[C/T]ACTGAACTCCCACTA | 55120 |
| rs755874039 | snp | C/T | 1.65732e-05 | 0.00287859 | intron-variant | FANCL | GRCh38.p7 | 2:58204081 | CATTCACAGAGTTCA[C/T]TTCACAAAGTATTTT | 55120 |
| rs755890804 | in-del | -/AA | 1.66974e-05 | 0.00288936 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159719 | AAAATTCCTTTTGAT[-/AA]TTTTTTAAGTTTCCA | 55120 |
| rs755891388 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180763 | ATTTTTTAACATAAG[C/T]GGTCTCACATCTCAC | 55120 |
| rs755910909 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237771 | CTCCTACCTCTAGGA[C/G]TTGGTGCCTAATTTC | 55120 |
| rs755923083 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58211388 | TAGCCTGCACACAGT[A/G]CTGGGACCCTGTGCC | 55120 |
| rs755927989 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213647 | GGGAGGCTGAGGCAG[G/T]AGAATCATTTCAGCC | 55120 |
| rs755952682 | snp | A/T | 1.66377e-05 | 0.00288419 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162855 | AATATCAAAACACTG[A/T]TAAAACTTACAGATT | 55120 |
| rs755965406 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191229 | TAAATTATACTCGCA[C/T]TAAAATAAATTTGCT | 55120 |
| rs756000370 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204173 | TGCTCTCTACCAGAA[A/G]CATCTTCTGCTTTTA | 55120 |
| rs756047554 | snp | A/G | 0.000115895 | 0.00761144 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162960 | TCCCTGAAAGCATGG[A/G]GAAAAAAATTATGCT | 55120 |
| rs756054987 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205424 | TATTTTCTTTCAGCT[A/G]TATCTGTAAATGCTT | 55120 |
| rs756055451 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190307 | TATCTGCCCACAGGA[C/T]CAAATGAAACATAGT | 55120 |
| rs756060574 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236629 | ATTTAAATCCAACCA[C/T]ATGAATAACCACGTT | 55120 |
| rs756102200 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178140 | AACCACACAGATTCA[C/T]AGCCAAATTCTACCA | 55120 |
| rs756129858 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233354 | CATGTCACATGCCAC[A/G]ATACTTTCCTGATTC | 55120 |
| rs756139184 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187345 | CCGCATGTTCTCACT[C/T]GTAGGTGAGAACTGA | 55120 |
| rs756168321 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174653 | AGTGTGTAGAGGGAA[A/G]TTTATAGCACTAAAT | 55120 |
| rs756221790 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231256 | TCATAATCAAGGTCT[C/G]AAATCCTTCATCTGT | 55120 |
| rs756228176 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233662 | CTCTAGGACTCCCAC[A/G]GCAACTCTTTTTAGA | 55120 |
| rs756229711 | snp | A/G | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188429 | AATTCTCTTAATTTC[A/G]GGGTTTTTTTGTTTT | 55120 |
| rs756329852 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197780 | AATACTTTAAAACAA[C/T]AAAAATGGAGTAGAA | 55120 |
| rs756339078 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198746 | AAACTAGATGTATTA[G/T]GGGCCGGGCGCGGTG | 55120 |
| rs756362960 | snp | A/C | 1.67186e-05 | 0.0028912 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159744 | GTTTCCAGCTCTTCA[A/C]CGAAATGTTGTATTC | 55120 |
| rs756372082 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167205 | GACAGAGCTAGACTC[C/T]GTCTCAAAAAGAAAA | 55120 |
| rs756417974 | snp | C/T | 5.11705e-05 | 0.00505793 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159838 | AACAAAGTTTGTGGA[C/T]ACTCTAAAAAATAAA | 55120 |
| rs756420413 | snp | A/T | 1.65425e-05 | 0.00287593 | stop-gained, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241250 | CCTCATACACGGTTT[A/T]CGACCGGTTCTGGGG | 55120 |
| rs756443718 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58228311 | ATATTCTCAAGTTTT[A/G]CATTGTTTTCAACAA | 55120 |
| rs756459114 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58232309 | CTCAAAACTGTCTTA[A/C]AAAAACTTTGTAGTT | 55120 |
| rs756470370 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195673 | AACAAAAAATTAGTA[A/T]CAAAATATAGATAAA | 55120 |
| rs756487177 | snp | A/G | 8.29731e-05 | 0.00644047 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241278 | GGGCAGAAGCAGGGG[A/G]CACTGGCGCAACAGG | 55120 |
| rs756487959 | snp | C/G | 1.66479e-05 | 0.00288508 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161599 | GAATGGTACCGTCAA[C/G]TTGATAAGCATAACA | 55120 |
| rs756503275 | snp | C/T | 1.95048e-05 | 0.00312282 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241355 | AAGCTCTAGACCTGC[C/T]GGGTCCTGCACATGC | 55120 |
| rs756522337 | in-del | -/AATA | | | intron-variant | FANCL | GRCh38.p7 | 2:58166190 | TGTACACACAACTTT[-/AATA]AATATTAATGTACAT | 55120 |
| rs756573827 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209194 | AAACTTTTTAATAAG[A/G]AATATGAAAGCTTTA | 55120 |
| rs756590256 | snp | A/G | 0.000115608 | 0.00760201 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221981 | TCTTCAATAAGGCTT[A/G]AGTAGAACTGGGGAG | 55120 |
| rs756622482 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221666 | GGAAAATTTAGAATA[C/T]AGTTGTATGTTCAGT | 55120 |
| rs756647476 | snp | C/G | 8.99386e-05 | 0.00670531 | intron-variant | FANCL | GRCh38.p7 | 2:58222081 | ATTAGCTGTGGAACG[C/G]AAGACAATGAACTGT | 55120 |
| rs756681755 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58166032 | CTCCCTGCTTCACAT[C/G]TCTTCCTACAGCGTT | 55120 |
| rs756695293 | snp | A/G | 3.31653e-05 | 0.00407204 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162888 | TCCAGGATAGCACGA[A/G]CTGGAAAATCAATTT | 55120 |
| rs756707104 | in-del | -/AA | 3.36409e-05 | 0.00410113 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159377 | GAAGACAGAAATATC[-/AA]GAGTCTCAAGAACCT | 55120 |
| rs756748685 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236694 | GCAATGACTATCATA[C/T]TGCATAACAAAGCAA | 55120 |
| rs756751763 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207118 | GCCAGTGGACTACAA[G/T]CACAAGTGATGTGTG | 55120 |
| rs756773258 | snp | A/G | 1.66538e-05 | 0.00288559 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162847 | CTGTCTGGAATATCA[A/G]AACACTGATAAAACT | 55120 |
| rs756826489 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191515 | ATAGTACAATGTATA[C/T]GTAGTCACCTTCCAC | 55120 |
| rs756899124 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161728 | GTGTGATATTTTGAT[A/G]CATGTATACAGTGTT | 55120 |
| rs756905041 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58171887 | CAGCACCCGGAAAAT[A/C]GGGTCACTCCCACCC | 55120 |
| rs756913424 | snp | A/G | 1.72704e-05 | 0.00293852 | intron-variant | FANCL | GRCh38.p7 | 2:58226803 | GATCAAAATATTTCC[A/G]ATTAATTTCATTTGC | 55120 |
| rs756968142 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169958 | GTGATGGGGAGAGTG[C/G]AACCAAGTTAAAAAA | 55120 |
| rs756980264 | snp | C/G | 1.66399e-05 | 0.00288438 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159391 | CAAGAGTCTCAAGAA[C/G]CTTTGAATGAAGTAA | 55120 |
| rs757023833 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212848 | ATTGAAATAAGAACA[A/G]AAATTATAACAATAG | 55120 |
| rs757041554 | in-del | -/AAG | 1.8332e-05 | 0.00302748 | intron-variant, cds-indel, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161645 | AGTAAAATCCTTCAA[-/AAG]AAAAATATTTATAAA | 55120 |
| rs757065505 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169098 | CAACACTCGAGCTCT[A/G]CTAAGGGACAGACTG | 55120 |
| rs757071062 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199854 | TTAGGCTTTCACTTT[C/T]TTCAGCCTCTTATTT | 55120 |
| rs757082773 | snp | A/T | 1.65529e-05 | 0.00287683 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198636 | AACAGGAAAATCCAC[A/T]AAATAATCTGGTGAT | 55120 |
| rs757088926 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58192582 | GATACAAATATCTTC[A/G]TAATAATGTAAACAC | 55120 |
| rs757145128 | in-del | -/A | 5.46612e-05 | 0.00522758 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163404 | TTTTATGACTCTATT[-/A]AAAAAACGTTTAAAT | 55120 |
| rs757189918 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191091 | GCATGCACAAGCATA[C/T]AAACACCCACATATT | 55120 |
| rs757211531 | snp | C/G | 5.44608e-05 | 0.00521799 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161642 | CATAGTAAAATCCTT[C/G]AAAAGAAAAATATTT | 55120 |
| rs757216388 | in-del | -/TATT | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160346 | GAGCCAATAGCAGAC[-/TATT]TATTAAGATGTTGAG | 55120 |
| rs757235886 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166145 | GCTTGATATACTACA[C/T]GTATGCAATAGTAAT | 55120 |
| rs757254495 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222107 | ACTGTTAATACCTGA[C/T]TGCAAAACATAATTT | 55120 |
| rs757277395 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179757 | ACTAAAGAGCTCCTT[A/C]ACAGCAAAAGAAACT | 55120 |
| rs757277846 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215926 | TTTAGAAAGTTCATA[A/G]TACAAGGAGAAATTA | 55120 |
| rs757304737 | in-del | -/CTAACAAA | 3.64325e-05 | 0.0042679 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159313 | TTGGATAACTCACGT[-/CTAACAAA]CTAAACTATATATGT | 55120 |
| rs757309110 | in-del | -/AC | 1.65669e-05 | 0.00287805 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159407 | CTTTGAATGAAGTAA[-/AC]AGTTTCCCACAAAAA | 55120 |
| rs757318350 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180819 | GGTTTTTTGTGTGTG[C/T]GTGCCCATTTGTAAT | 55120 |
| rs757321657 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236313 | GTAGAAAACAGTGCA[A/G]GACAGTGAAGTAACA | 55120 |
| rs757325992 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190039 | TTGCAATATCTCCAT[C/G]AGGTATCTTTAAACA | 55120 |
| rs757332234 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179146 | CAATATCGTGAAAAT[G/T]GCCATACTGCCCTAA | 55120 |
| rs757419935 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58205852 | GATAAAAGGGGGAAG[-/A]AGAAACTTTAAACCA | 55120 |
| rs757429080 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202149 | GTTAATATTCCTATA[-/T]GTGGAGTTTTTGTTG | 55120 |
| rs757437166 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210589 | TAACTTATTTCATCA[A/T]TAACTCAAAAGTCCA | 55120 |
| rs757478584 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235171 | AGAGAAATGCATGGA[A/G]AGTAGAGAAATATAC | 55120 |
| rs757501573 | snp | C/T | 3.30568e-05 | 0.00406538 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159636 | AGATGTTTATTATTA[C/T]CGCATCATCATACCT | 55120 |
| rs757507955 | in-del | -/CT | | | intron-variant | FANCL | GRCh38.p7 | 2:58211034 | TGGAAGATGGTGGCC[-/CT]CTTCTCACAGCTACA | 55120 |
| rs757518527 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58224037 | AGAAAGCTAAAATAC[A/G]GGATTTCATTTTTAT | 55120 |
| rs757520179 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185326 | TACCCTGACTGTTCC[A/G]TATACGGGCTTGTCC | 55120 |
| rs757560351 | snp | A/G | 1.82174e-05 | 0.00301801 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163528 | ATTACCTAGAATGAA[A/G]CAAGATTAAATCTTT | 55120 |
| rs757568770 | in-del | -/ATC | | | intron-variant | FANCL | GRCh38.p7 | 2:58221343 | CTGAATAGCAAACAA[-/ATC]ATCACATACTTTTTC | 55120 |
| rs757597691 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200405 | TTACAAAATCTCTTT[A/T]CCTTCTAAAATGTCA | 55120 |
| rs757622310 | snp | A/C | 1.67531e-05 | 0.00289418 | intron-variant | FANCL | GRCh38.p7 | 2:58165917 | TTATATGGTACTCTA[A/C]CAATAGCAGATAATC | 55120 |
| rs757650938 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184765 | CAGCTAAGCCTTAGC[A/G]TGGTATGAGAAGGAA | 55120 |
| rs757683704 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221984 | TCAATAAGGCTTGAG[C/T]AGAACTGGGGAGGAG | 55120 |
| rs757714548 | snp | A/G | 0.000106891 | 0.00730986 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241326 | CATGGCTCGAAGTCC[A/G]GAGAAACACAGAAAA | 55120 |
| rs757716369 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168224 | AGGCAGAAGGCAGGT[A/G]ATTTCTGCATTTCCA | 55120 |
| rs757726228 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58166380 | AGGCAGAGTATGAAA[A/C]GGTTTTACACATTTT | 55120 |
| rs757733149 | in-del | -/TTTAT | 1.6619e-05 | 0.00288257 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159678 | GTTAGTATTTCTTGC[-/TTTAT]TTTTTCTCTGAAGAT | 55120 |
| rs757774955 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58211145 | TCCATGAGGGCCCCA[A/C]CCCTGCAGCAAACTT | 55120 |
| rs757822598 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167334 | CCTGTAAGTTTAGGT[A/G]ACAGAATCCAGAAAT | 55120 |
| rs757842951 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241366 | CTGCTGGGTCCTGCA[A/C]ATGCGCAGTCCGCTG | 55120 |
| rs757858944 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231092 | GGCTTGAAAGACTCT[-/G]GCTGCCCAAGTTTTC | 55120 |
| rs757892335 | snp | A/G | 4.95683e-05 | 0.00497812 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198609 | CTGAGGTGTCCAGGA[A/G]GCACAAAATGGAACA | 55120 |
| rs757940244 | snp | A/G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242791 | TAAATAAATTTGCAC[A/G/T]CTTTTCTCTTATTAA | 55120 |
| rs757940427 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239031 | TAATTAAATAAATGA[C/G]AAAGCAGGCAATGCT | 55120 |
| rs757945007 | in-del | -/AAAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58202240 | CTATACCTTTTTCCT[-/AAAA]AAAAAAAAAAAAAAA | 55120 |
| rs757978832 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58207528 | CCCACTCTTGACCAT[A/C]TGCCTACCTCTGAAT | 55120 |
| rs757995529 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226902 | GCTATATCTACATCT[A/G]AAAACTATAAGAAAT | 55120 |
| rs758057758 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58164498 | CTGGTAATGGCTCCA[C/G]ACAGTACTTTCACGT | 55120 |
| rs758062496 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208317 | AGCAAATATAAAACT[C/G]AAGTATAAAATCTAA | 55120 |
| rs758091193 | in-del | -/CTTT | | | intron-variant | FANCL | GRCh38.p7 | 2:58165264 | AATTCTTTCTCTGTG[-/CTTT]CTGTTTACTCTTCAG | 55120 |
| rs758092508 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179158 | aatggccatactgcc[C/T]taagtaatttataga | 55120 |
| rs758190742 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214764 | TGATCTGCCCCACCT[C/T]AGCCCCCCAAAGTAC | 55120 |
| rs758190931 | snp | C/G | 1.65141e-05 | 0.00287346 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159535 | AAATACACTTCCACA[C/G]TCAGCACGGGGATCA | 55120 |
| rs758231122 | snp | A/T | 1.6513e-05 | 0.00287336 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159603 | TTCCCAGTTTACTCT[A/T]AGTGAAGAGACAAAC | 55120 |
| rs758315047 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182576 | AAATAAAACCCATTT[G/T]ATACAACTAACCCAC | 55120 |
| rs758332810 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171402 | AGGGAAATTTATAAC[A/G]AAATGCCCACATGAG | 55120 |
| rs758335437 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213944 | TAAAGGCTCCATATC[A/G]GAGCTGCCCTATGGG | 55120 |
| rs758336022 | in-del | -/TCT | 3.29478e-05 | 0.00405867 | cds-indel, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165784 | GCTCAAGTACCCAGG[-/TCT]TCTCATCGATTTCAT | 55120 |
| rs758337132 | in-del | -/G | 1.675e-05 | 0.00289391 | frameshift-variant, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222034 | TTGTCTATTCTTTAA[-/G]GCAACTTCCTGTTTA | 55120 |
| rs758404552 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169848 | GTGTGAAGACAAGAT[A/T]AGAGAAAAAAGAATG | 55120 |
| rs758546412 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180609 | AATACCTAATGTAGA[C/T]GTCGGGTTGATGGGT | 55120 |
| rs758577664 | snp | A/T | 1.76325e-05 | 0.00296916 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241323 | CGCCATGGCTCGAAG[A/T]CCGGAGAAACACAGA | 55120 |
| rs758597677 | in-del | -/ACACA | 1.65511e-05 | 0.00287668 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159433 | CAAAAAATCAGCTAT[-/ACACA]ATTCCCAAACTCATT | 55120 |
| rs758619310 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223558 | CTCCTACTGTAGAAC[C/T]GTAACAGCTAAAAAG | 55120 |
| rs758639881 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58172445 | CATTCGTGGTTCAAG[A/C]AAATCTGCTGTTCTG | 55120 |
| rs758687156 | in-del | -/T | 3.32508e-05 | 0.00407729 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159681 | GTATTTCTTGCTTTA[-/T]TTTTTTCTCTGAAGA | 55120 |
| rs758696645 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179908 | TATCTAAAAGTAGGC[A/G]AAGGATATGAACAGA | 55120 |
| rs758712673 | snp | A/C | 1.75919e-05 | 0.00296574 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163093 | CAGATTAAAAAAAAA[A/C]AATTTAATAATTGCA | 55120 |
| rs758728377 | snp | C/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165735 | CTACCTAATGCAATT[C/G]TGCGTGCTGTTGCAC | 55120 |
| rs758732387 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217704 | GACATAAAGCAAAAT[C/T]TTGAGGAACAAAAAC | 55120 |
| rs758754024 | snp | C/T | 1.66313e-05 | 0.00288364 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229822 | GACTTACCTGTTGTA[C/T]TATTCGATGGTATCC | 55120 |
| rs758757153 | snp | A/G | 1.65789e-05 | 0.0028791 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221955 | ACTTATCCCAACCAA[A/G]AGTTCCTATCTCTTC | 55120 |
| rs758850921 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165803 | CTCATCGATTTCATC[C/T]ATAACATCCCAGAAT | 55120 |
| rs758900730 | in-del | -/AAAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58202454 | CTAAGCTAAATTGAG[-/AAAT]AAAGATTCTAATAAA | 55120 |
| rs758914385 | snp | A/G | 1.6588e-05 | 0.00287988 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160195 | CTGCAAATTTTAAAA[A/G]ATAAAGGAGAAGCGT | 55120 |
| rs758917546 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198752 | GATGTATTAGGGGCC[A/G]GGCGCGGTGGCTCAC | 55120 |
| rs758933787 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58241099 | CAAGAGCCGTTACGC[A/G]CCGCCCCTCTCAATC | 55120 |
| rs758989239 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58224281 | TTGTTTATTAAAATT[A/G]TAATAAAAAGATAAA | 55120 |
| rs759004553 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230932 | ATTCTCTAACCACCT[C/T]TTTTTCTTCAAAATA | 55120 |
| rs759014427 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58190386 | AAAAGTGAAAGAAAG[A/C]AAGCTCCTCAAGCAC | 55120 |
| rs759021953 | snp | C/G | 5.02913e-05 | 0.00501429 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241296 | CTGGCGCAACAGGCT[C/G]GCTTCCGTCACCGCC | 55120 |
| rs759025839 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215035 | ACAGAAATAAAACTA[G/T]AACATTTCCTCTGTC | 55120 |
| rs759046648 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167870 | TTAGGGGGTAGACAT[C/G]AAAACTATTATATCA | 55120 |
| rs759088086 | snp | A/G | 5.00455e-05 | 0.00500202 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159701 | TTCTCTGAAGATGAT[A/G]CCAAAATTCCTTTTG | 55120 |
| rs759092214 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197076 | TAGCATACATCAAAA[C/T]ACCAAAAGCAAATTA | 55120 |
| rs759217429 | snp | A/T | 1.67228e-05 | 0.00289156 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232107 | CCTAAGGTGGAAGTC[A/T]CTTCCCTGTGGAAAA | 55120 |
| rs759217526 | in-del | -/TAAT | 0.00574453 | 0.0532847 | FANCL, VRK2 | 2 | allele_origin=T(germline)/(germline) | 2:58159793 | CAGACATTTTTAAGG[-/TAAT]TAATTGGCTTTAAAA | 55120 |
| rs759231330 | in-del | -/AAC | | | utr-variant-3-prime, intron-variant, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159315 | GGATAACTCACGTCT[-/AAC]AAACTAAACTATATA | 55120 |
| rs759243979 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167023 | TAGAGACCATCCTGG[C/T]CAATAAGGTGAAACC | 55120 |
| rs759297087 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179596 | AACACAATATGGATT[A/G]AAGACTTAAACATAA | 55120 |
| rs759317234 | in-del | -/TGTT | 1.65214e-05 | 0.0028741 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159623 | AGAGACAAACGCAGA[-/TGTT]TGTTTATTATTATCG | 55120 |
| rs759365110 | snp | A/C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178176 | ACAAAGAAGAGCTGG[A/C/T]ACCATTCCTTCTGAA | 55120 |
| rs759388980 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216655 | TTTAGTTTTCAAAAA[A/G]TATTAGGGATGCCAA | 55120 |
| rs759396046 | snp | C/T | 1.68241e-05 | 0.00290031 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222036 | GTCTATTCTTTAAGG[C/T]AACTTCCTGTTTAAA | 55120 |
| rs759420748 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58199008 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAATCTCC | 55120 |
| rs759425129 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198174 | CATTATAGAAGGTGT[A/G]TTTATAAATAAATGC | 55120 |
| rs759459944 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185997 | AAGTGCAGCTAAGAA[C/G]TCAGTGCCTATTACC | 55120 |
| rs759467155 | snp | A/T | 1.7594e-05 | 0.00296592 | intron-variant | FANCL | GRCh38.p7 | 2:58221930 | TTAAAACATATTTTA[A/T]AACAGACATACTTAT | 55120 |
| rs759474073 | snp | A/C | 1.79348e-05 | 0.00299451 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163410 | TGACTCTATTAAAAA[A/C]CGTTTAAATCTCAGA | 55120 |
| rs759496775 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223046 | CTATCAAATTGAGAT[C/T]ATATTAGAAAGAACA | 55120 |
| rs759513031 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185052 | AAACAAGAGAAACTA[C/G]AAAACTACCTCTATA | 55120 |
| rs759533198 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167765 | GGTAGATACATTAAA[C/T]ATTATTTTTACATTC | 55120 |
| rs759586585 | snp | A/G | 6.73718e-05 | 0.00580357 | intron-variant | FANCL | GRCh38.p7 | 2:58229888 | ATCTAAAATTTTAAT[A/G]AGACAAAATGGTTTA | 55120 |
| rs759588855 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221175 | CCTAGGCAACAGAGC[A/G]AGACTCGGTCTCAAA | 55120 |
| rs759596979 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227605 | CTCTCGATGTCCTCT[C/T]GATGTCCAGCCACTT | 55120 |
| rs759652074 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214543 | GTTGACAGGGTCTCA[A/C]TGTCACCTAGACTGA | 55120 |
| rs759671554 | in-del | -/GAG | 1.64977e-05 | 0.00287203 | intron-variant | FANCL | GRCh38.p7 | 2:58204237 | CAAGTCTGGTGAGCA[-/GAG]GAGAATAAAAAATGA | 55120 |
| rs759711454 | snp | A/G | 3.30874e-05 | 0.00406726 | intron-variant | FANCL | GRCh38.p7 | 2:58165877 | TTATTAAGGAGCTCT[A/G]TGAAAAAAATGAAAG | 55120 |
| rs759740975 | in-del | -/A | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163394 | CTAGGCAAGGATTTT[-/A]TGACTCTATTAAAAA | 55120 |
| rs759745363 | snp | A/C/G | 5.27768e-05 | 0.00513674 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241319 | TCACCGCCATGGCTC[A/C/G]AAGTCCGGAGAAACA | 55120 |
| rs759786662 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58193644 | ATTAACCAATTTAAG[A/T]GTGAATAAAATTCCA | 55120 |
| rs759795718 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182374 | TGGAAGAATGAAGAA[C/T]AGCCATGCTTGTTTC | 55120 |
| rs759924910 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178830 | CTGTATATTTACAAA[A/T]CCCTATCATCTCAGC | 55120 |
| rs759945648 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210261 | CATGTGGCTGGGGAA[A/G]GCTCACAATCATGGT | 55120 |
| rs759962245 | snp | A/C | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188275 | TTGTCTACCTTTATG[A/C]AAATACCATATTATC | 55120 |
| rs759998890 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239810 | GATCAGTAAAATGGA[-/G]AAAATGTAAACTGGT | 55120 |
| rs760008652 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235746 | AAATTAAAACAATTA[A/G]ATTTCATACGTTCAA | 55120 |
| rs760013811 | snp | C/G/T | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158866 | TAACACTATAGCTAC[C/G/T]CCTGAGGCAGTTTTC | 55120 |
| rs760023098 | snp | C/G | | | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159376 | AGAAGACAGAAATAT[C/G]AAGAGTCTCAAGAAC | 55120 |
| rs760088188 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228391 | TGTAGAGCAAATCCT[G/T]GACTATCCCTTCTTC | 55120 |
| rs760090192 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203432 | AAAGTTGGACATCCT[A/G]GTTTTCTTCAAATTC | 55120 |
| rs760145730 | snp | C/T | 1.65282e-05 | 0.00287469 | utr-variant-3-prime, stop-gained, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159466 | TTTTATGAGCCTCAT[C/T]AAGATTTTACCAGTC | 55120 |
| rs760157185 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243052 | AAGGACGGCCATGCT[A/G]CATGTTTTCCTATAA | 55120 |
| rs760163232 | snp | A/G | 3.35233e-05 | 0.00409396 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163063 | TCAGCTTAATTCCCA[A/G]GGGTTTTACCACTTC | 55120 |
| rs760167123 | snp | A/G | 1.8745e-05 | 0.0030614 | intron-variant | FANCL | GRCh38.p7 | 2:58221922 | AAAGGCATTTAAAAC[A/G]TATTTTAAAACAGAC | 55120 |
| rs760183197 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58193671 | TCCACTACTGTAAGT[A/C]CTCCAACAAAAACAG | 55120 |
| rs760221884 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168766 | AGCTTGGTGGGGGAA[G/T]GGACATCCACCATTA | 55120 |
| rs760281226 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163223 | TTATACAGTTCAGAA[C/T]GCTGAGACATTGTCA | 55120 |
| rs760322966 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197147 | CCATTGTGGGGAGAT[A/T]GGGACTTTAAAAAAA | 55120 |
| rs760336067 | in-del | -/CTAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58175194 | ATTCACAGCCGAATT[-/CTAC]CAGAGGTACAAGGAG | 55120 |
| rs760337641 | in-del | -/ATATTTTAACAAAGTTTGT | 3.38241e-05 | 0.00411229 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159816 | CTTTAAAAAGAGAAC[-/ATATTTTAACAAAGTTTGT]GGACACTCTAAAAAA | 55120 |
| rs760395951 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163670 | ATGTAATGGTAAATA[C/T]AATTGAACCAAAAGA | 55120 |
| rs760396835 | snp | A/T | 1.65138e-05 | 0.00287343 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159560 | GGATCACAGACTTAG[A/T]AAGTTCAACTGGACT | 55120 |
| rs760406786 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168087 | TCAAAGTTCAGTAAG[C/T]ATTTTGCAGGGAGAT | 55120 |
| rs760447231 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181996 | AAAACACACAAATAC[A/G]TCTTCTCAGAAAAAA | 55120 |
| rs760502912 | in-del | -/ATG | | | cds-indel, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160136 | GGACATTCACCAAAT[-/ATG]ATGTTAAAACTCTGT | 55120 |
| rs760523667 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238339 | TTTGATCAAGAACTA[C/T]CATCCAAGTTGTTCG | 55120 |
| rs760536836 | snp | C/G | 5.54544e-05 | 0.00526537 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241342 | GAGAAACACAGAAAA[C/G]CTCTAGACCTGCTGG | 55120 |
| rs760540055 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207096 | GTTGGCATATAACTA[C/T]ATTTTGGCCAGTGGA | 55120 |
| rs760542163 | snp | A/C | 3.30961e-05 | 0.0040678 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160150 | TATGATGTTAAAACT[A/C]TGTCTACTAGTTAGT | 55120 |
| rs760587361 | snp | C/T | 9.97871e-05 | 0.00706283 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161487 | CCTATGTTGTGTTAG[C/T]GGAAAAAAGTCTTGA | 55120 |
| rs760590237 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172899 | TTTGAAAAAAATTTA[C/G]ACGAATGCATAACTA | 55120 |
| rs760593303 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208085 | TAAGTCTATGTTAAG[G/T]TGGACGTCTCACTTT | 55120 |
| rs760615591 | snp | G/T | 8.6175e-05 | 0.00656354 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241315 | TCCGTCACCGCCATG[G/T]CTCGAAGTCCGGAGA | 55120 |
| rs760641420 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204029 | AAGCATGATATATGT[A/T]TTTTTAGATGTAACT | 55120 |
| rs760725236 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201982 | ATAAAAAAAATTCAG[C/T]ATTCCACTTAAAACT | 55120 |
| rs760744126 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214606 | CTCGACCTACCCAGG[A/C]TCAAGTGATCCTCCC | 55120 |
| rs760770525 | snp | C/T | 1.68744e-05 | 0.00290463 | intron-variant | FANCL | GRCh38.p7 | 2:58229797 | CTGAAAACATAAACC[C/T]TTTAAAAAGGACTTA | 55120 |
| rs760788175 | snp | A/G | 1.6585e-05 | 0.00287962 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226762 | ATCATAAAGCTCATT[A/G]GATCAGGAGAGTGCT | 55120 |
| rs760788528 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58203644 | CTCTGCAAATTCTTA[A/C]AATACTTAAAAAACC | 55120 |
| rs760796412 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215410 | AGTACACTTACAATT[A/G]TATGTAACATCTATT | 55120 |
| rs760804603 | snp | A/G | 1.76593e-05 | 0.00297142 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159345 | ATATGTATTTTTTCC[A/G]TAGGAAAGCACAAGG | 55120 |
| rs760858938 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58235035 | ATGGGAGTATTTTCA[A/G]GCTGCAAGATAGGGA | 55120 |
| rs760912654 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | FANCL | GRCh38.p7 | 2:58165693 | AAAATAAAACACCTA[A/G]AAACAAACCCTTAAT | 55120 |
| rs760951123 | in-del | -/T | 1.84558e-05 | 0.00303769 | intron-variant | FANCL | GRCh38.p7 | 2:58221924 | GGCATTTAAAACATA[-/T]TTTTAAAACAGACAT | 55120 |
| rs760964833 | in-del | -/TCATCATACCTGTCC | 1.65312e-05 | 0.00287495 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159640 | TTTATTATTATCGCA[-/TCATCATACCTGTCC]TCATCATACCTGTCC | 55120 |
| rs761006496 | in-del | -/TATC | | | intron-variant | FANCL | GRCh38.p7 | 2:58213057 | CAGCAAGGCCAGCAT[-/TATC]TAACAAGGATTTTTC | 55120 |
| rs761016847 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183651 | ATGACAATGACAATT[C/T]TTTATTCTCTTCTTT | 55120 |
| rs761020505 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236034 | GTGCCCAACACAGAG[C/G]ACAGAAAAGGAGGAA | 55120 |
| rs761025575 | in-del | -/AT | | | intron-variant | FANCL | GRCh38.p7 | 2:58190318 | AGGACCAAATGAAAC[-/AT]AGTCACCTCATGTGT | 55120 |
| rs761039364 | in-del | -/G | 1.65737e-05 | 0.00287864 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241274 | TCTGGGGCAGAAGCA[-/G]GGGGCACTGGCGCAA | 55120 |
| rs761047182 | snp | C/T | 1.67002e-05 | 0.00288961 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162817 | AGAGAAGCATTTAAA[C/T]TTCATTATGCAATAC | 55120 |
| rs761106745 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223124 | CTTCAATTTCGTTCT[A/G]AATCTGCTTTATGAT | 55120 |
| rs761124053 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189813 | TGTGATCTTTTGTGC[C/T]ATGATGACACTTAAA | 55120 |
| rs761125806 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204785 | ATAAATTTTCTTTCT[A/G]CACGATATATAGCTT | 55120 |
| rs761138735 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211059 | AGCTACACTAGGCGG[C/T]GCCTCAGTAGGGACT | 55120 |
| rs761175143 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58232347 | AATCAAAACACTCAG[A/C]TAAGACTTTGTTTTT | 55120 |
| rs761177091 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190779 | ATTAATTAATTAATA[C/T]TGTCTCAGTGTCTCT | 55120 |
| rs761210597 | snp | C/T | 1.65021e-05 | 0.00287241 | intron-variant | FANCL | GRCh38.p7 | 2:58204127 | GTTTAACGAGGCACA[C/T]ACCTTTGCCTTCAAC | 55120 |
| rs761259325 | snp | A/G/T | 3.31424e-05 | 0.00407066 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162900 | CGAGCTGGAAAATCA[A/G/T]TTTCTAAAACATCTT | 55120 |
| rs761291501 | snp | A/G | 0.000102747 | 0.00716679 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241312 | GCTTCCGTCACCGCC[A/G]TGGCTCGAAGTCCGG | 55120 |
| rs761327399 | snp | C/T | 1.65583e-05 | 0.00287731 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162934 | AATTTTGTAACACAC[C/T]ATTTTCTGGATCCCT | 55120 |
| rs761344488 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219554 | ACGGTGCAGAAACCC[A/G]ACAAATACTACCTCA | 55120 |
| rs761371487 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58173155 | AAAGACCAAACCTAC[A/G]TCTGATTTGTGTACC | 55120 |
| rs761490451 | snp | A/G | 0.000395915 | 0.0140642 | intron-variant | FANCL | GRCh38.p7 | 2:58204239 | AGTCTGGTGAGCAGA[A/G]GAGAATAAAAAATGA | 55120 |
| rs761509078 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209886 | CAAAATATCACCATT[A/T]ATCAGCTTCTAAGAT | 55120 |
| rs761535925 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227706 | CGGGTTTTTATAGGC[A/G]CAAGATGGAGGTATG | 55120 |
| rs761562505 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195157 | CAAGCAGAATTGTTT[A/T]CAGCCAGCCAATTAA | 55120 |
| rs761573995 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186327 | GGTATATTTGGACCC[C/T]TGTCCTACATATCTT | 55120 |
| rs761593798 | in-del | -/CTTGCTTAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58165120 | AAGTCACATGTTTTG[-/CTTGCTTAT]AATGAAAATACACAG | 55120 |
| rs761689573 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | FANCL | GRCh38.p7 | 2:58165686 | ATAATACAAAATAAA[A/G]CACCTAAAAACAAAC | 55120 |
| rs761704892 | snp | A/G | 1.69106e-05 | 0.00290775 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159813 | TGGCTTTAAAAAGAG[A/G]ACATATTTTAACAAA | 55120 |
| rs761714477 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58165571 | CCTAAAATATTTACA[C/T]TTAAATGTGTAGCCA | 55120 |
| rs761722210 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240824 | AAAATAATTAGCCCA[A/G]ATTCCCGAGTGAACT | 55120 |
| rs761742545 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165753 | CGTGCTGTTGCACTC[C/T]GTGGAGGTTTTTCTG | 55120 |
| rs761768579 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206326 | TTGCATGTAGGCAGA[-/T]TATTTAGAAACATGG | 55120 |
| rs761769619 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182392 | CCATGCTTGTTTCAG[C/T]CCAAATATTACCAGA | 55120 |
| rs761841521 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178635 | ATATCATACTGAATG[G/T]GCAAAAGCTGGAAGC | 55120 |
| rs761857472 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58180908 | TATTAATGAGATAAC[A/C]TTAAAATAATAAATG | 55120 |
| rs761858505 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227990 | AAGAGGAGTATAAAA[C/T]ATAAAAATCAGGCAA | 55120 |
| rs761923433 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236269 | ATATTCTATTTACAG[A/G]GAAACAAAGAAAAGA | 55120 |
| rs761946214 | snp | C/T | 1.65078e-05 | 0.00287291 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161679 | AGCGTATGTGTCTCA[C/T]TAACTTATTCGTTGT | 55120 |
| rs761950134 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204951 | AATTCTGTAAAAATA[C/T]GGTCCCTTGAGTAGC | 55120 |
| rs761951196 | in-del | -/TTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58165662 | CTGTCATTGTTAGAT[-/TTA]TTATTTTCATAATAC | 55120 |
| rs762011579 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204293 | GGGAACTGGAGATGG[C/T]TGAATTTGAAATGAA | 55120 |
| rs762052029 | snp | C/T | 1.80683e-05 | 0.00300563 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159326 | GTCTAACAAACTAAA[C/T]TATATATGTATTTTT | 55120 |
| rs762055361 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162078 | AATATTCCCATATCA[C/T]ACATTGTTATAATGT | 55120 |
| rs762067554 | in-del | -/A | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160775 | GATTTTATATAAGGT[-/A]AATAGATGCCTCTGC | 55120 |
| rs762069385 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169506 | CTTTTCTCCAACGGA[C/T]CACAACTCCTCGCCA | 55120 |
| rs762108335 | snp | G/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161065 | GCATTCTTCTCAACA[G/T]GAAAAGTAGTAGTAT | 55120 |
| rs762156045 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58176737 | AAGGACTTCATGTCT[-/A]AAACACCAAAAGCAA | 55120 |
| rs762159653 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171543 | CAGAACTGAAGGAGA[C/T]AGAGACACGAAAAAC | 55120 |
| rs762172533 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168894 | TAGCCAGACTGCCTC[A/G]CCAGATTCCTCCTCT | 55120 |
| rs762187856 | snp | C/T | 1.71255e-05 | 0.00292617 | intron-variant | FANCL | GRCh38.p7 | 2:58198562 | TTTAATTACTTAAAA[C/T]AAATTTAAGAATTTA | 55120 |
| rs762210449 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58168178 | ATGGCCAAACAGGAA[A/C]AGCTCCAGTCTGCAG | 55120 |
| rs762238736 | snp | C/T | 1.65759e-05 | 0.00287883 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161587 | ACACTTGATCAGGAA[C/T]GGTACCGTCAAGTTG | 55120 |
| rs762249762 | snp | A/C | 1.66402e-05 | 0.00288441 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232093 | TCAGGCAACACTATC[A/C]TAAGGTGGAAGTCTC | 55120 |
| rs762338908 | snp | A/G | 3.31411e-05 | 0.00407056 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241222 | TGGGCGGGTACCTGA[A/G]CCGAGATGAATCCCT | 55120 |
| rs762366997 | in-del | -/TTATGAGATG | 9.94596e-05 | 0.00705123 | intron-variant, downstream-variant-500B, frameshift-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160078 | AAAGCTAGGCACATT[-/TTATGAGATG]TTATGAGATGTGATT | 55120 |
| rs762375937 | snp | A/C | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164298 | ACACTGTAGAATAAG[A/C]CTTTCACTAAGGCTG | 55120 |
| rs762397392 | snp | A/T | 1.69095e-05 | 0.00290765 | intron-variant | FANCL | GRCh38.p7 | 2:58198668 | CTGCAGGATACTATT[A/T]AAAAAGCATAACATT | 55120 |
| rs762415491 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188385 | ACTATCACAGGACCT[C/T]TGCAGCCTTTGCACA | 55120 |
| rs762438552 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208644 | CTGCTTCAAAAGACA[C/G]ACTGAAGACCTTCAT | 55120 |
| rs762451147 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234435 | CAAATGTCATAAAGG[G/T]CAAAGAAAAAGCAAG | 55120 |
| rs762463456 | snp | C/T | 3.41939e-05 | 0.0041347 | intron-variant | FANCL | GRCh38.p7 | 2:58198683 | AAAAAAGCATAACAT[C/T]AGACCATTTTTGCTT | 55120 |
| rs762488803 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179426 | AGGCCTCAGAAATAA[C/T]GCCACACATCTACAA | 55120 |
| rs762491763 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210008 | ACAAACTTGAAAAGT[A/T]CAACTAGTTGAAGTG | 55120 |
| rs762520467 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233007 | CAATTAAATGTACCC[C/T]ATAACCTTTACTTTC | 55120 |
| rs762564285 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239945 | TAAGATTTAAATAAA[C/T]TGCTAAGGCAGGTAC | 55120 |
| rs762598250 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184899 | ATAGCCAAGTACATT[C/G]TACTTCGCCTTCCAC | 55120 |
| rs762613868 | snp | C/T | 1.66114e-05 | 0.00288192 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241282 | AGAAGCAGGGGGCAC[C/T]GGCGCAACAGGCTCG | 55120 |
| rs762637652 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58177816 | AGAAAAAGAAAAAAC[-/A]AAAAAAAACCCAAAT | 55120 |
| rs762682564 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178749 | CAATCAGGCAAGAGA[A/C]AGAAATAAAAGGTAT | 55120 |
| rs762692084 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58215733 | AGCATCATTTCCGCC[A/C]ATCTCTTGAGGATAG | 55120 |
| rs762727214 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58173302 | TGCCACAAAGATACT[C/T]TCGAGAAGAGCAACT | 55120 |
| rs762777524 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198913 | GGGCGCCTGTAGTCC[C/G]AGCTACTTGGGAGGC | 55120 |
| rs762815455 | snp | A/G | 3.29848e-05 | 0.00406095 | intron-variant | FANCL | GRCh38.p7 | 2:58165676 | ATTTATTTTCATAAT[A/G]CAAAATAAAACACCT | 55120 |
| rs762818038 | snp | A/G | 1.72513e-05 | 0.0029369 | intron-variant | FANCL | GRCh38.p7 | 2:58222053 | ACTTCCTGTTTAAAA[A/G]AAGAAAACCTGAATT | 55120 |
| rs762820766 | in-del | -/C | 3.95538e-05 | 0.00444695 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241360 | CTAGACCTGCTGGGT[-/C]CTGCACATGCGCAGT | 55120 |
| rs762839658 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58165453 | AGTTACCTGTTCCAC[A/G]ATTCCTGTGCTAATT | 55120 |
| rs762876936 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230244 | CATGTATTTGAAAAA[A/G]CATGTGTAGCAATAT | 55120 |
| rs762881693 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58196771 | TCTACATCTAAAACA[A/C]AAAGAAACTCATAAA | 55120 |
| rs762885563 | snp | A/G | | | | | GRCh38.p7 | 2:58243416 | CTGGATAGGTAATCC[A/G]CAGAAATTAATTATT | 55120 |
| rs762900406 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58195531 | AAAAATATATGAAAG[A/G]TTTTATTTGAAACAC | 55120 |
| rs762904548 | snp | C/T | 5.17942e-05 | 0.00508866 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163503 | CTACCTCTATATTTA[C/T]GGAAACATTATTACC | 55120 |
| rs762929927 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58185018 | GTAGGACTGCAGGAG[-/A]AAAAAAGAGGCACAG | 55120 |
| rs762940521 | snp | A/T | 1.65674e-05 | 0.00287809 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226744 | AAAAGCATCTTCAAC[A/T]CCATCATAAAGCTCA | 55120 |
| rs762965800 | snp | C/T | 1.67019e-05 | 0.00288975 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159714 | ATACCAAAATTCCTT[C/T]TGATAATTTTTTAAG | 55120 |
| rs763012232 | snp | A/C | 1.66158e-05 | 0.0028823 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161503 | GGAAAAAAGTCTTGA[A/C]AATATTTTTATTTTT | 55120 |
| rs763041336 | in-del | -/TAG | 1.65496e-05 | 0.00287655 | cds-indel, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160162 | ACTCTGTCTACTAGT[-/TAG]TAGTCCTCTCAGCCA | 55120 |
| rs763044655 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215170 | ATACCTAAAGAATGA[C/G]TAGGTCCATGACATC | 55120 |
| rs763048371 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58240991 | AGGCGTGGCCCCAGC[A/C]CCGCTCCACGCCGCG | 55120 |
| rs763057392 | snp | C/T | 1.65512e-05 | 0.00287669 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161575 | GAGAATTATCACACA[C/T]TTGATCAGGAATGGT | 55120 |
| rs763108021 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162465 | CCCTTGAACAACATG[A/G]GTTTGAACTGCACAG | 55120 |
| rs763197509 | in-del | -/ATC | | | intron-variant | FANCL | GRCh38.p7 | 2:58197040 | TTAATAGAAAAAAAA[-/ATC]AACATAGTATTTTAC | 55120 |
| rs763207894 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58209954 | AATCTCCCAGTTCGC[A/C]CATCAGATTTAGTAA | 55120 |
| rs763218703 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206765 | TTTGTTAAACTTTAA[A/G]ACGCAATTTAAATAA | 55120 |
| rs763225905 | snp | A/T | 1.87009e-05 | 0.00305779 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163395 | TAGGCAAGGATTTTA[A/T]GACTCTATTAAAAAA | 55120 |
| rs763239730 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58191987 | GAGCCAGAATTTGAT[C/G]CAGACTTTAAGACTC | 55120 |
| rs763308728 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213606 | GGCCAGGCATGGCAG[C/T]GAACACCTGTTAATC | 55120 |
| rs763317098 | snp | A/T | 1.69717e-05 | 0.002913 | intron-variant | FANCL | GRCh38.p7 | 2:58232017 | CCTGTCCCACCAAAA[A/T]GCAAAAATGCACGTT | 55120 |
| rs763367770 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214287 | TCTGTTCCTTTTTCT[C/T]CTACATTAGAACAAT | 55120 |
| rs763400472 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233243 | ACACGAAAAATAGAA[C/G]AACTATTCTATATAG | 55120 |
| rs763401780 | snp | C/T | 1.65211e-05 | 0.00287407 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159480 | TCAAGATTTTACCAG[C/T]CCAGATATATTCAAG | 55120 |
| rs763404839 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58182134 | ATGTAGCATTTCCTT[A/C]AACTATGGATATAGG | 55120 |
| rs763417767 | in-del | -/AA | 0.000231983 | 0.0107674 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163084 | TTACCACTTCAGATT[-/AA]AAAAAAAAAATTTAA | 55120 |
| rs763424708 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201880 | AATAGAACAAATGCA[C/T]TTATTTACTGTATAT | 55120 |
| rs763432147 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58169536 | AGCAAGGGAACAAAA[A/C]TGGACAGAGAATGAG | 55120 |
| rs763452293 | snp | G/T | 1.66377e-05 | 0.00288419 | intron-variant | FANCL | GRCh38.p7 | 2:58165901 | ATGAAAGTTGAATAA[G/T]TTATATGGTACTCTA | 55120 |
| rs763456981 | snp | G/T | 1.65158e-05 | 0.00287361 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159553 | AGCACGGGGATCACA[G/T]ACTTAGAAAGTTCAA | 55120 |
| rs763459893 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172111 | GAAGCTCGAACTGGG[C/T]GGAGCCCACCACAGC | 55120 |
| rs763468021 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171545 | GAACTGAAGGAGATA[A/G]AGACACGAAAAACCC | 55120 |
| rs763479620 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58226477 | ACATTTTATTTCTTC[A/C]CCACCTGCCCAACAC | 55120 |
| rs763483048 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168985 | TCCCATCTCCCTGGG[A/T]CAGAGCACGTGGGGA | 55120 |
| rs763505840 | in-del | -/T | 1.70124e-05 | 0.00291649 | intron-variant | FANCL | GRCh38.p7 | 2:58198676 | ACTATTAAAAAAGCA[-/T]TAACATTAGACCATT | 55120 |
| rs763515392 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218185 | TTGCTTACAAATTTA[C/T]AGCCTTAAATTAATA | 55120 |
| rs763523035 | snp | A/C | 1.66269e-05 | 0.00288326 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232088 | AATCTTCAGGCAACA[A/C]TATCCTAAGGTGGAA | 55120 |
| rs763546341 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231567 | TCTTCTCCAGAAATA[C/T]TTAGAGGCAGAATTG | 55120 |
| rs763566148 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58196521 | TATGACCCAATTAAA[A/C]CTGAAACTTAAATTT | 55120 |
| rs763568885 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172258 | AGCAGTGGTTCTCTC[A/T]GCACGCACCTGGAGA | 55120 |
| rs763610692 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217128 | CATTACATATATATA[C/T]ATTTTTATATATAGA | 55120 |
| rs763615183 | snp | A/C/G/T | 6.62412e-05 | 0.00575476 | stop-gained, missense, synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241225 | GCGGGTACCTGAGCC[A/C/G/T]AGATGAATCCCTCAT | 55120 |
| rs763660087 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58205461 | CAAAAAAAATTAGAA[C/T]GTCTTTATCACGTTT | 55120 |
| rs763670271 | snp | C/G | 3.4562e-05 | 0.0041569 | intron-variant | FANCL | GRCh38.p7 | 2:58198696 | ATTAGACCATTTTTG[C/G]TTCTGTGTGTTAATA | 55120 |
| rs763696738 | in-del | -/AGG | | | intron-variant | FANCL | GRCh38.p7 | 2:58170994 | TTAACAAGGATATTC[-/AGG]AGTTGAACTCAGCTC | 55120 |
| rs763723949 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242348 | CAGTGGTTCTCAAAA[C/T]GTGATCCTAGAACCT | 55120 |
| rs763774770 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58230678 | TCTTGGTCTTCAAAT[A/C]CCCATAACCATCCCT | 55120 |
| rs763813243 | snp | A/T | 1.75486e-05 | 0.0029621 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163512 | TATTTATGGAAACAT[A/T]ATTACCTAGAATGAA | 55120 |
| rs763837257 | snp | A/G | 1.66593e-05 | 0.00288607 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162843 | AATACTGTCTGGAAT[A/G]TCAAAACACTGATAA | 55120 |
| rs763840016 | snp | A/C | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160203 | TTTAAAAGATAAAGG[A/C]GAAGCGTCAGCATGA | 55120 |
| rs763874552 | snp | A/G | 3.3413e-05 | 0.00408722 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159716 | ACCAAAATTCCTTTT[A/G]ATAATTTTTTAAGTT | 55120 |
| rs763893895 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58238705 | CAATACTGTCTAATT[A/G]CAATACAAGAAAAAT | 55120 |
| rs763912617 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58218011 | GGATGATTTCTGACA[A/G]AAGTAGACTTAAACT | 55120 |
| rs763963728 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181469 | GTATCCATTTACTGG[A/T]ACTTATGGAACACTT | 55120 |
| rs763972614 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237801 | CCCTCCTTTTGAATA[C/T]AGACTAAGAAACTTG | 55120 |
| rs763993192 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207103 | TATAACTACATTTTG[A/G]CCAGTGGACTACAAG | 55120 |
| rs764000842 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215726 | AAAAAAAAGCATCAT[C/T]TCCGCCAATCTCTTG | 55120 |
| rs764011851 | in-del | -/GA | | | intron-variant | FANCL | GRCh38.p7 | 2:58180900 | AGTACTAATATTAAT[-/GA]GATAACATTAAAATA | 55120 |
| rs764085319 | snp | C/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162808 | TTTTCACTGAGAGAA[C/G]CATTTAAACTTCATT | 55120 |
| rs764090694 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58235627 | CATCCAATCAAGATA[C/T]ACCAAGCACATATAT | 55120 |
| rs764091316 | snp | A/T | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158921 | TTGCCCACTGTACAG[A/T]GGACACTTCTCAGTT | 55120 |
| rs764122820 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188451 | TTTTGTTTTTTGGTT[C/T]TTTTTTGAGATAGGG | 55120 |
| rs764122832 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203761 | CAAAAGAAATTTATA[C/G]TAACAGCTGAATGCA | 55120 |
| rs764174197 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189874 | AGTTGTTTTCAATTC[C/T]GATCTTTTTTATTCT | 55120 |
| rs764186056 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202023 | TAAGATTTTGCATAA[C/T]ATACTCTTAACATAC | 55120 |
| rs764186411 | snp | C/G | 1.65559e-05 | 0.00287709 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161578 | AATTATCACACACTT[C/G]ATCAGGAATGGTACC | 55120 |
| rs764193884 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223909 | ATTTATTGGTGATTA[C/T]AGTATAGGAACCCTA | 55120 |
| rs764207302 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58194386 | ATCTGACCTGTATGT[-/A]AAAATTCTAAAGCAT | 55120 |
| rs764273540 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215413 | ACACTTACAATTATA[C/T]GTAACATCTATTTCT | 55120 |
| rs764333125 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168118 | GAATTCTCTAAAAAA[C/T]ATTTTTAAAAATAAA | 55120 |
| rs764351688 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202608 | CTATAAAAGTGCTTC[A/G]TAACTACAGATGTTG | 55120 |
| rs764373985 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58197161 | TTGGGACTTTAAAAA[A/C]AAAAACAATAAAAGG | 55120 |
| rs764374441 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240329 | AAGACTATGCGTGAT[-/G]GTGGGGAAGTGGGCA | 55120 |
| rs764375123 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214649 | CGAGAAGCTAGGTGC[A/G]TACCACCACACCTAA | 55120 |
| rs764378405 | snp | A/G/T | 3.34265e-05 | 0.00408807 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241292 | GGCACTGGCGCAACA[A/G/T]GCTCGCTTCCGTCAC | 55120 |
| rs764386146 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180217 | TCCAGCAATCCCATT[A/G]TGGGGTATATACCCA | 55120 |
| rs764393410 | snp | C/T | 1.65493e-05 | 0.00287652 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221961 | CCCAACCAAGAGTTC[C/T]TATCTCTTCAATAAG | 55120 |
| rs764407713 | in-del | -/C | 3.36287e-05 | 0.00410039 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241301 | GCAACAGGCTCGCTT[-/C]CGTCACCGCCATGGC | 55120 |
| rs764408622 | in-del | -/AAA | 1.71369e-05 | 0.00292714 | intron-variant, utr-variant-3-prime, cds-indel | FANCL, VRK2 | GRCh38.p7 | 2:58159844 | GTTTGTGGACACTCT[-/AAA]AAATAAAATTGCTTT | 55120 |
| rs764413990 | snp | G/T | 0.000345411 | 0.0131372 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163421 | AAAAACGTTTAAATC[G/T]CAGATGTCATACCAT | 55120 |
| rs764474023 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58176840 | CCATCAGAGTGAACA[-/G]GCAACCTACAAAATG | 55120 |
| rs764475167 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170453 | AAATGTAAAGACCAT[C/G]AACACTATGAAGAAA | 55120 |
| rs764501439 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168150 | ATAGCTAACATTCTT[G/T]GTGGCTGGCAAGATG | 55120 |
| rs764507447 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58211098 | GGACTCCAATCCCAC[A/G]CTTCCCTTCCGCATT | 55120 |
| rs764517006 | in-del | -/CCTTTGAATGAAGTAAACAGTTT | 1.66474e-05 | 0.00288503 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159390 | CAAGAGTCTCAAGAA[-/CCTTTGAATGAAGTAAACAGTTT]CCTTTGAATGAAGTA | 55120 |
| rs764560935 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212148 | TTAATTGGACTTACA[A/G]TTCCACATGGCTGGG | 55120 |
| rs764561595 | snp | A/G | 1.75468e-05 | 0.00296194 | intron-variant | FANCL | GRCh38.p7 | 2:58198551 | CAACTGTACTTTTTA[A/G]TTACTTAAAACAAAT | 55120 |
| rs764571426 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58187330 | ACAGAAAACCAAACA[A/C]CGCATGTTCTCACTC | 55120 |
| rs764591934 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58179683 | GGCATGGGCAAAGAC[G/T]TCATGACTAAAACAC | 55120 |
| rs764596577 | in-del | -/CTTAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58210572 | CAGGCCCCCCAAAGT[-/CTTAA]CTTATTTCATCATTA | 55120 |
| rs764629926 | snp | A/G | 1.66106e-05 | 0.00288184 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161504 | GAAAAAAGTCTTGAC[A/G]ATATTTTTATTTTTT | 55120 |
| rs764649246 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236184 | AAGCTACACCAAGGT[A/G]CAACACACATCAAAG | 55120 |
| rs764661559 | snp | C/T | 1.66546e-05 | 0.00288566 | intron-variant | FANCL | GRCh38.p7 | 2:58165905 | AAGTTGAATAAGTTA[C/T]ATGGTACTCTACCAA | 55120 |
| rs764661561 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213068 | GCATTATCTAACAAG[A/G]ATTTTTCTGTATCAG | 55120 |
| rs764678435 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219813 | AAGTGGCAGGTTGGA[C/T]AGTCAGGCAAAGCAT | 55120 |
| rs764738818 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223179 | ACAGATCCGTACAGC[C/T]GAGAATATCAATATG | 55120 |
| rs764758671 | snp | A/G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207143 | TGTGTGCTTTTGGGG[A/G/T]TTCATTTATAACAGA | 55120 |
| rs764760346 | snp | A/G | 1.66879e-05 | 0.00288855 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159705 | CTGAAGATGATACCA[A/G]AATTCCTTTTGATAA | 55120 |
| rs764782273 | snp | A/T | 1.6607e-05 | 0.00288153 | intron-variant | FANCL | GRCh38.p7 | 2:58241215 | CAACCACTGGGCGGG[A/T]ACCTGAGCCGAGATG | 55120 |
| rs764858631 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231769 | CCTTTTGTTCTCCCT[C/T]TATATACCTGTTCAG | 55120 |
| rs764955577 | snp | C/T | 1.67517e-05 | 0.00289406 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221943 | TAAAACAGACATACT[C/T]ATCCCAACCAAGAGT | 55120 |
| rs764969578 | snp | C/G | 1.65263e-05 | 0.00287452 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198606 | TACCTGAGGTGTCCA[C/G]GAGGCACAAAATGGA | 55120 |
| rs765022740 | snp | A/G | 3.33394e-05 | 0.00408272 | stop-gained, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161602 | TGGTACCGTCAAGTT[A/G]ATAAGCATAACAAAT | 55120 |
| rs765040501 | snp | C/T | 1.65252e-05 | 0.00287443 | intron-variant | FANCL | GRCh38.p7 | 2:58204260 | TAAAAAATGATCACA[C/T]CGGGGAGAGCTGGAG | 55120 |
| rs765049506 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186976 | TTGGTGGGAGTGTGA[A/G]CTAGTTCAACCATTG | 55120 |
| rs765058568 | snp | G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241397 | GCGCTCGGACGCCGC[G/T]GAGCGGAAACCCCAG | 55120 |
| rs765059646 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196862 | CTGGAAAGAGTAACA[C/T]AACCTAGCTATAATA | 55120 |
| rs765079182 | snp | C/T | 1.79001e-05 | 0.00299161 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163411 | GACTCTATTAAAAAA[C/T]GTTTAAATCTCAGAT | 55120 |
| rs765102215 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169788 | CCGAATCAATCAAGC[A/G]GAAGAAAGGATATCA | 55120 |
| rs765176056 | in-del | -/GGA | 1.65248e-05 | 0.00287439 | cds-indel, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221993 | CTTGAGTAGAACTGG[-/GGA]GGAGGAGGTAGTGCA | 55120 |
| rs765201430 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190899 | AAGATGAGGGGGGAA[C/T]ATTTTCTAGCTCTAA | 55120 |
| rs765209343 | snp | A/G | 1.65119e-05 | 0.00287327 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159585 | TGGACTTTGGCCTAC[A/G]ATTTCCCAGTTTACT | 55120 |
| rs765240084 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58237504 | ATATCTGTACTAGAA[A/T]AGAAGAAAGATCTCA | 55120 |
| rs765250178 | in-del | -/GAT | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160414 | ACTGGTTTATAACCA[-/GAT]GATTATGGGCCCCTT | 55120 |
| rs765265718 | snp | C/T | 1.72424e-05 | 0.00293614 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163501 | GTCTACCTCTATATT[C/T]ATGGAAACATTATTA | 55120 |
| rs765296461 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239814 | AGTAAAATGGAGAAA[A/G]TGTAAACTGGTGAAT | 55120 |
| rs765321485 | snp | G/T | 1.65864e-05 | 0.00287974 | intron-variant | FANCL | GRCh38.p7 | 2:58165888 | CTCTGTGAAAAAAAT[G/T]AAAGTTGAATAAGTT | 55120 |
| rs765352168 | in-del | -/TTTAT | 1.6619e-05 | 0.00288257 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159677 | GTTAGTATTTCTTGC[-/TTTAT]TTTATTTTTTCTCTG | 55120 |
| rs765408457 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206459 | CATAACCATGATGAA[C/T]ATAAAGAGGGAGAGA | 55120 |
| rs765436582 | snp | C/G | 1.66236e-05 | 0.00288297 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161496 | TGTTAGCGGAAAAAA[C/G]TCTTGACAATATTTT | 55120 |
| rs765437556 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204968 | GTCCCTTGAGTAGCA[C/T]AAGCTACTGCCAAAA | 55120 |
| rs765453781 | snp | G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243260 | TCTTCTCAAGTGCTA[G/T]GTCTTTTTGGAAAGC | 55120 |
| rs765505083 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186403 | CCCCAGAAGGCAAAG[C/T]CAGAGACAAGGACAT | 55120 |
| rs765616967 | snp | G/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161090 | TAGTATTGGATATAT[G/T]CTATTCTTAAATGCA | 55120 |
| rs765639691 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58226315 | ATTAAACAGTACATA[C/T]GTAACAGTATACATA | 55120 |
| rs765657023 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58168262 | TACCGGCTCACCTCA[C/T]TGGGACTGGTTAGAT | 55120 |
| rs765659741 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58198701 | ACCATTTTTGCTTCT[C/G]TGTGTTAATATCACT | 55120 |
| rs765683135 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169564 | GAGTTTGACAAACTG[A/G]CAGAAGTAGGCTTCA | 55120 |
| rs765718795 | snp | C/T | 1.66468e-05 | 0.00288498 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229817 | AAAAGGACTTACCTG[C/T]TGTACTATTCGATGG | 55120 |
| rs765718948 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58190198 | GTAAAGAACATATCA[A/C]CTCTTCTATACTTAA | 55120 |
| rs765729177 | in-del | -/CT | 0.00011581 | 0.00760864 | frameshift-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160148 | AATATGATGTTAAAA[-/CT]CTGTCTACTAGTTAG | 55120 |
| rs765769907 | snp | A/G | 1.6855e-05 | 0.00290297 | intron-variant | FANCL | GRCh38.p7 | 2:58229890 | CTAAAATTTTAATGA[A/G]ACAAAATGGTTTATT | 55120 |
| rs765773076 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224869 | AATATCAATACAAAC[C/T]CATAATTATATTCTT | 55120 |
| rs765778508 | snp | A/C | 1.65258e-05 | 0.00287448 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159468 | TTATGAGCCTCATCA[A/C]GATTTTACCAGTCCA | 55120 |
| rs765795452 | snp | C/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242518 | TCCTTCTTCCCTGAG[C/G]CGGGTCATTGGATCC | 55120 |
| rs765800516 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58181343 | TAATATCTGGAATAG[A/T]CATAACTAAGCTTTG | 55120 |
| rs765808434 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214879 | GGAAGTCCATAAATA[A/T]TATTAGCAGGGTAAA | 55120 |
| rs765822164 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212226 | TACATGGATGGCAGC[A/T]GGCAAAGAGAGAATG | 55120 |
| rs765839703 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211166 | CAGCAAACTTCTGCC[G/T]GGGCATCCAGGAATT | 55120 |
| rs765846258 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58239950 | TTTAAATAAACTGCT[A/C]AGGCAGGTACAAATT | 55120 |
| rs765872787 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229279 | TGCTTCAGTAACTGA[-/T]TTTTTTTTTCTAATC | 55120 |
| rs765881788 | snp | A/G | 3.30262e-05 | 0.0040635 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159568 | GACTTAGAAAGTTCA[A/G]CTGGACTTTGGCCTA | 55120 |
| rs765926796 | snp | C/G | | | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165775 | GTTTTTCTGGCTCAA[C/G]TACCCAGGTCTTCTC | 55120 |
| rs765929160 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58172325 | TTGACCCCTGACCCC[-/T]GAGCAGCCTAACTGG | 55120 |
| rs765943099 | snp | G/T | 1.6517e-05 | 0.00287372 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159505 | TTCAAGAAGTCAAGA[G/T]CTCCATCTTGGTATA | 55120 |
| rs765991434 | snp | C/T | 1.68738e-05 | 0.00290458 | intron-variant | FANCL | GRCh38.p7 | 2:58165924 | GTACTCTACCAATAG[C/T]AGATAATCTTTTACT | 55120 |
| rs766070924 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208659 | GACTGAAGACCTTCA[C/T]GTTTGAATAAAGCAT | 55120 |
| rs766104531 | snp | C/G | 8.64775e-05 | 0.00657505 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241316 | CCGTCACCGCCATGG[C/G]TCGAAGTCCGGAGAA | 55120 |
| rs766120470 | snp | A/G | 3.3753e-05 | 0.00410796 | intron-variant | FANCL | GRCh38.p7 | 2:58232030 | AATGCAAAAATGCAC[A/G]TTTATAACTAAACAC | 55120 |
| rs766136636 | snp | A/G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58177911 | GATGAAGGGGATATC[A/G/T]CCACTGATCCTACAG | 55120 |
| rs766167644 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58171609 | TTTGAAAAGAGTAAC[A/C]AAATAGGGGATTGGA | 55120 |
| rs766203041 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178819 | AGATGACATGACTGT[A/G]TATTTACAAAACCCT | 55120 |
| rs766210836 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58240998 | GCCCCAGCCCCGCTC[A/C]ACGCCGCGCGCCTCC | 55120 |
| rs766220225 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184999 | TTGGTATGCCTTAAC[A/G]TGGGGTAGGACTGCA | 55120 |
| rs766227781 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58173325 | GAGCAACTCCAAGAC[A/C]CATAATTGTCAGATT | 55120 |
| rs766231526 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215794 | GAATCTGGGGAAAGG[C/T]AGGCCCAGAACCTGG | 55120 |
| rs766302163 | snp | A/G | 6.59979e-05 | 0.00574409 | intron-variant | FANCL | GRCh38.p7 | 2:58204246 | TGAGCAGAGGAGAAT[A/G]AAAAATGATCACACC | 55120 |
| rs766319030 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212368 | ACCGGGTCCCTCCTG[C/T]AACACATGGGAATTG | 55120 |
| rs766344718 | in-del | -/AAG | 3.4356e-05 | 0.00414449 | intron-variant | FANCL | GRCh38.p7 | 2:58222051 | CAACTTCCTGTTTAA[-/AAG]AAGAAAACCTGAATT | 55120 |
| rs766351502 | snp | G/T | 1.67744e-05 | 0.00289602 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163065 | AGCTTAATTCCCAGG[G/T]GTTTTACCACTTCAG | 55120 |
| rs766353592 | snp | C/T | 1.81727e-05 | 0.00301431 | intron-variant | FANCL | GRCh38.p7 | 2:58221926 | GCATTTAAAACATAT[C/T]TTAAAACAGACATAC | 55120 |
| rs766392441 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58226421 | GTAGGACTACCTAAT[A/C]TCTTCTTAGATGTTA | 55120 |
| rs766392516 | snp | C/G/T | 3.29507e-05 | 0.00405887 | intron-variant | FANCL | GRCh38.p7 | 2:58165702 | CACCTAAAAACAAAC[C/G/T]CTTAATCCTCCTTGT | 55120 |
| rs766417160 | in-del | -/T | 8.88755e-05 | 0.00666557 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163096 | ATTAAAAAAAAAAAA[-/T]TTAATAATTGCATGC | 55120 |
| rs766419213 | snp | G/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163771 | TAGATTGCAATTCTG[G/T]TCAACTGTATTAAAG | 55120 |
| rs766420612 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168986 | CCCATCTCCCTGGGA[C/G]AGAGCACGTGGGGAA | 55120 |
| rs766440818 | in-del | -/AGAT | 1.65861e-05 | 0.00287972 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160193 | ACTGCAAATTTTAAA[-/AGAT]AGATAAAGGAGAAGC | 55120 |
| rs766459541 | snp | C/T | 3.36542e-05 | 0.00410195 | intron-variant | FANCL | GRCh38.p7 | 2:58229800 | AAAACATAAACCTTT[C/T]AAAAAGGACTTACCT | 55120 |
| rs766570507 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237677 | TAGATGTATCGGGGG[A/G]AAAAATGAGACATAA | 55120 |
| rs766618785 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165774 | GGTTTTTCTGGCTCA[A/G]GTACCCAGGTCTTCT | 55120 |
| rs766620360 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202042 | CTCTTAACATACAGT[A/T]AACGTTTCAACTATT | 55120 |
| rs766631841 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58225053 | AAATGAATAAATGAA[A/C]CTGGGGCAACTGGTA | 55120 |
| rs766631917 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238521 | ATAACTTTAAGCCAA[C/T]AAAATCAGAAACCTA | 55120 |
| rs766641449 | snp | C/G/T | 3.41397e-05 | 0.00413146 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159840 | CAAAGTTTGTGGACA[C/G/T]TCTAAAAAATAAAAT | 55120 |
| rs766758036 | snp | C/T | 1.65474e-05 | 0.00287636 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160158 | TAAAACTCTGTCTAC[C/T]AGTTAGTAGTCCTCT | 55120 |
| rs766780791 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206536 | ACCTACTACTTTCTG[A/T]ACTTCACATTGTTGC | 55120 |
| rs766785357 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58217791 | TCAGGACAAGCGGAC[-/A]AAAAAAAAAAAATAA | 55120 |
| rs766818402 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187128 | CACATATGTTTATTG[C/T]GGCATGATTCACAAT | 55120 |
| rs766854274 | snp | C/T | 1.76101e-05 | 0.00296728 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159346 | TATGTATTTTTTCCA[C/T]AGGAAAGCACAAGGA | 55120 |
| rs766882824 | snp | G/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242077 | ACCTACTAAAATATT[G/T]ACCATATGATTATTT | 55120 |
| rs766932264 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169541 | GGGAACAAAACTGGA[C/T]AGAGAATGAGTTTGA | 55120 |
| rs766967805 | snp | C/T | | | | | GRCh38.p7 | 2:58243468 | AGTCCAAAATCAAGA[C/T]GCAAGGACAAGATTT | 55120 |
| rs766981249 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197121 | TCTATTTTGCTATGT[G/T]TTCTCAACTTCCATT | 55120 |
| rs766995602 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58185105 | AGAAGCTAAGTTTAA[C/T]AGGGAAATATTCCCT | 55120 |
| rs767038810 | snp | A/G | 0.000395876 | 0.0140635 | intron-variant | FANCL | GRCh38.p7 | 2:58204241 | TCTGGTGAGCAGAGG[A/G]GAATAAAAAATGATC | 55120 |
| rs767048675 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184457 | ACAAATTCTTAACAG[A/G]AATAGCAAAACAACT | 55120 |
| rs767072559 | snp | A/G | 1.656e-05 | 0.00287745 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162935 | ATTTTGTAACACACT[A/G]TTTTCTGGATCCCTG | 55120 |
| rs767214256 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58195624 | ATACAAAGTTAAAAG[A/G]CATGCCACAGAGATA | 55120 |
| rs767230450 | snp | A/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161375 | ATGAAGCACATAAGC[A/T]TCTGGAATAAACTGG | 55120 |
| rs767236818 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236517 | CAAAGGAGATAAAAC[A/G]GAATTACAAAAAAGA | 55120 |
| rs767244500 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233276 | ATCTGTGCTGTTATC[C/T]GAAAGAATAAAATTC | 55120 |
| rs767254287 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211051 | CTTCTCACAGCTACA[C/T]TAGGCGGTGCCTCAG | 55120 |
| rs767270220 | in-del | -/TTA | 1.65229e-05 | 0.00287423 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159627 | GACAAACGCAGATGT[-/TTA]TTATTATCGCATCAT | 55120 |
| rs767326425 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58230266 | TAGCAATATTATCTT[-/C]AAATTCCCGATTAAT | 55120 |
| rs767343464 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167073 | AAAAATTAGCTGGGC[A/G]TAGTGGCACGCGCCC | 55120 |
| rs767356418 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191145 | AAAAAAAAATTCAAA[C/T]AGACATATAGACATA | 55120 |
| rs767380648 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205214 | GACCAGGTACTATAT[A/G]ATGATAACATGGGCT | 55120 |
| rs767424993 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201720 | AAACCAAAAAATTTA[A/T]CTGGTTTACTTCTAC | 55120 |
| rs767450055 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159815 | GCTTTAAAAAGAGAA[C/T]ATATTTTAACAAAGT | 55120 |
| rs767489178 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58174277 | TGAACTCAGCTCTGC[A/C]CCAAGCAGACCTAAT | 55120 |
| rs767512286 | snp | A/T | 1.78493e-05 | 0.00298736 | intron-variant | FANCL | GRCh38.p7 | 2:58222077 | CTGAATTAGCTGTGG[A/T]ACGCAAGACAATGAA | 55120 |
| rs767513074 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186074 | AAGTCAAAGGAAGCC[A/G]ACAGCAACTGTGAAG | 55120 |
| rs767516722 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199049 | AAAAAAAAAAAAGAA[A/T]AACGAGATATATTGG | 55120 |
| rs767554404 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215916 | AAAAACAAGATTTAG[A/G]AAGTTCATAATACAA | 55120 |
| rs767594845 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202363 | TTTGTCCAAATTCAC[A/G]ATCTAGAACTAACTT | 55120 |
| rs767602826 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58221328 | AGCTAAATTCAGAAA[A/C]TGAATAGCAAACAAA | 55120 |
| rs767617831 | in-del | -/C | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159915 | GTTTGGAAAACACTT[-/C]TGAAGTTTCAGATCA | 55120 |
| rs767722695 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221146 | TGAACCCGGGAGGCG[C/G]AGCTTGCAATCAGCC | 55120 |
| rs767745600 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58189606 | TGAGCTAGGAAAGCA[C/G]TTAAGCAGGAAAGTA | 55120 |
| rs767774736 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58213845 | GTTAATTTTGCAAAT[A/C]GTCCATTTTATTCGT | 55120 |
| rs767777932 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210275 | AGGCTCACAATCATG[G/T]TGCAATGCAAGGAGG | 55120 |
| rs767779534 | snp | C/T | 1.65721e-05 | 0.0028785 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226756 | AACTCCATCATAAAG[C/T]TCATTAGATCAGGAG | 55120 |
| rs767781467 | in-del | -/CT | 3.73183e-05 | 0.00431946 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163398 | GCAAGGATTTTATGA[-/CT]CTATTAAAAAACGTT | 55120 |
| rs767833500 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242136 | CATCACGTTTGAGCC[C/T]TACTATTTGAAAAAC | 55120 |
| rs767843173 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187182 | AATGTCCATCAATGA[C/T]AGACTGGATTAAGAA | 55120 |
| rs767851051 | snp | C/T | 1.82437e-05 | 0.00302018 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163529 | TTACCTAGAATGAAA[C/T]AAGATTAAATCTTTT | 55120 |
| rs767861553 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159887 | TAGTGTCATAGAATA[A/G]TGTCATAGTACAGTT | 55120 |
| rs767949582 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198580 | ATTTAAGAATTTACC[A/T]GAGGAGAATTTACCT | 55120 |
| rs767965537 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58165995 | TAGCTACAAAGTAGA[C/G]TCCAGTAAACAGTAG | 55120 |
| rs767966517 | snp | G/T | 2.14254e-05 | 0.00327296 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161684 | ATGTGTCTCACTAAC[G/T]TATTCGTTGTACATA | 55120 |
| rs767970128 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210264 | GTGGCTGGGGAAGGC[A/T]CACAATCATGGTGCA | 55120 |
| rs767983260 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58236050 | CAGAAAAGGAGGAAC[-/A]AAAAAAAAAAAAAGA | 55120 |
| rs767985150 | in-del | -/AAT | 6.70646e-05 | 0.00579032 | intron-variant | FANCL | GRCh38.p7 | 2:58165918 | ATATGGTACTCTACC[-/AAT]AATAGCAGATAATCT | 55120 |
| rs768000672 | snp | A/G | 1.65789e-05 | 0.0028791 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161588 | CACTTGATCAGGAAT[A/G]GTACCGTCAAGTTGA | 55120 |
| rs768023871 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58200241 | TGTATGCCATATTTA[A/G]AAATCGTGATTATCT | 55120 |
| rs768039421 | in-del | -/AAACT | 1.81843e-05 | 0.00301526 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159317 | TAACTCACGTCTAAC[-/AAACT]AAACTAAACTATATA | 55120 |
| rs768056738 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169340 | CGGAAAACTAACAAA[C/G]AGAAAGCAATAGCAT | 55120 |
| rs768120986 | snp | C/G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233591 | AGACAGGGTACACGA[C/G/T]AAACCTCAAATTACC | 55120 |
| rs768253825 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213994 | TTCACACAGAATGCC[C/T]GAGTGGTGTTATGTA | 55120 |
| rs768303607 | snp | A/C | 1.66239e-05 | 0.00288299 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160215 | AGGAGAAGCGTCAGC[A/C]TGATTACAAATTACA | 55120 |
| rs768308581 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58164827 | CAGTTAGACTTTTTG[-/A]AACCAGGAAAGTACC | 55120 |
| rs768324044 | in-del | -/CTT | | | intron-variant | FANCL | GRCh38.p7 | 2:58234892 | GATTTATCTTCCCTC[-/CTT]ATTTAAAAATTGGAC | 55120 |
| rs768342310 | in-del | -/G | 1.65809e-05 | 0.00287926 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163001 | TAAAATCACCAAAAA[-/G]TAAAAATTATATTGC | 55120 |
| rs768347495 | snp | A/G | 1.79968e-05 | 0.00299968 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241329 | GGCTCGAAGTCCGGA[A/G]AAACACAGAAAAGCT | 55120 |
| rs768352905 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209638 | ACACCTACTTTACAC[C/T]AGGAACTATATGAGT | 55120 |
| rs768401257 | snp | A/C | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204224 | GTATCCGCATACACA[A/C]GTCTGGTGAGCAGAG | 55120 |
| rs768411699 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168782 | GGACATCCACCATTA[C/G]TGAGGCTTGAGTACG | 55120 |
| rs768416928 | snp | A/G | 1.8274e-05 | 0.00302269 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159300 | ACAAAATAAATACTT[A/G]GATAACTCACGTCTA | 55120 |
| rs768419528 | snp | C/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242995 | TGAGGATCTCTGCAG[C/G]GGCAGGACATAACAC | 55120 |
| rs768421377 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219008 | AGCAACAAGCACCCA[C/T]AGTGCCCACATCCTA | 55120 |
| rs768460578 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58208126 | AAATAAATAACTTTC[A/C]TTCACTTAAATAAAA | 55120 |
| rs768480846 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58213313 | ATGTGGACAGCACAG[A/T]TCAGGTCTCAGCTTT | 55120 |
| rs768538410 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208959 | TATGTGAGCCACTGA[C/T]CTACTCCAAAGTCAA | 55120 |
| rs768568679 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205844 | AAGTGCATGATAAAA[C/G]GGGGAAGAAGAAACT | 55120 |
| rs768596921 | snp | A/C/T | 3.31424e-05 | 0.00407066 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58226751 | TCTTCAACTCCATCA[A/C/T]AAAGCTCATTAGATC | 55120 |
| rs768626260 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229215 | CATAAAAAGAAAGGC[A/G]ATTCTAAAAACTATT | 55120 |
| rs768651890 | snp | A/T | 1.81916e-05 | 0.00301587 | intron-variant | FANCL | GRCh38.p7 | 2:58226834 | ACAATAAATATTCTA[A/T]CCACTAAAACTGTAA | 55120 |
| rs768704605 | snp | A/C | 1.65583e-05 | 0.00287731 | intron-variant | FANCL | GRCh38.p7 | 2:58204089 | GAGTTCATTTCACAA[A/C]GTATTTTCTGATCAC | 55120 |
| rs768745077 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216259 | CCATCCTGAACCCAC[C/T]TGGGCCCTTTGCCAA | 55120 |
| rs768795836 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58185746 | GCCTTAAAATGTATC[C/T]CATTTTTGAATTATT | 55120 |
| rs768806440 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225767 | GCCAAATCCAGAATG[C/T]AGAAGATTTTATAGG | 55120 |
| rs768814501 | snp | C/G | 5.04359e-05 | 0.00502149 | splice-acceptor-variant | FANCL | GRCh38.p7 | 2:58198663 | TGATTCTGCAGGATA[C/G]TATTAAAAAAGCATA | 55120 |
| rs768819241 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171950 | CGGCACACCAGGAGA[C/T]TACATCCCGCTTGGA | 55120 |
| rs768838648 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170385 | AGAGCTCCTGAAGGA[C/T]GCGTGAAATATGCAA | 55120 |
| rs768855398 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58197589 | TACCACCTTATATCT[A/G]TGTTATAGTTTACAG | 55120 |
| rs768872237 | snp | A/G | 1.68145e-05 | 0.00289948 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163469 | AAGCACTCAGGAAGC[A/G]TAGTAGGATGCCTGG | 55120 |
| rs768970308 | in-del | -/C | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158841 | CGTCTGTATAGCTTT[-/C]CAAGAGACATAACAC | 55120 |
| rs768971115 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216764 | ACAGGTACCTTCATA[C/T]CTTGACCTCTGACCT | 55120 |
| rs768975596 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230189 | TTAAATAAAACCAAC[A/G]GTTTTGATAACAATA | 55120 |
| rs768982809 | in-del | -/GT | | | intron-variant | FANCL | GRCh38.p7 | 2:58198079 | TATGCATGGGTGTGG[-/GT]GTGAGTGGGTGTGTT | 55120 |
| rs768994925 | snp | C/T | 3.31664e-05 | 0.00407211 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159665 | CTGTCCTTTTGATGT[C/T]AGTATTTCTTGCTTT | 55120 |
| rs769041851 | snp | C/T | 1.66302e-05 | 0.00288355 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232089 | ATCTTCAGGCAACAC[C/T]ATCCTAAGGTGGAAG | 55120 |
| rs769052968 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58172623 | AAAGACATCCACACC[-/A]AAAACCCATCTGTAC | 55120 |
| rs769058926 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214593 | AGCTCCCTGCAGCCT[C/T]GACCTACCCAGGCTC | 55120 |
| rs769069044 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200224 | TCACTGGAAAAACAA[-/T]TTGTATGCCATATTT | 55120 |
| rs769084666 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237309 | CTAAATTATAAATCA[A/G]TAACAAAAAGATATC | 55120 |
| rs769151137 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234541 | CCAGAGTACATATAA[C/T]TGGAGATCTTGGAAA | 55120 |
| rs769156276 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178669 | CCCTTTGCAAACCAG[A/C]ACAAGACAAGGATGC | 55120 |
| rs769215579 | snp | C/T | 3.95296e-05 | 0.00444559 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163550 | TAAATCTTTTAGAAG[C/T]AGAACAGCTCATCAA | 55120 |
| rs769220500 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206359 | GTTGTAAACATGAAT[A/G]TTTCAAAGTATTTGT | 55120 |
| rs769259739 | snp | C/G | 1.6951e-05 | 0.00291122 | intron-variant | FANCL | GRCh38.p7 | 2:58241187 | GCTGCAAGAGGCTCT[C/G]TTAGCTAGAAAGCAA | 55120 |
| rs769285566 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163284 | CGAGATCGCGCCATT[A/G]CACTACATACTGGGC | 55120 |
| rs769300042 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179681 | TTGGCATGGGCAAAG[A/C]CTTCATGACTAAAAC | 55120 |
| rs769319753 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222567 | ACTATTCTTCAAGCA[A/G]GTAAGTCGGAGTATT | 55120 |
| rs769338663 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162067 | TGGGCATCAGTAATA[C/T]TCCCATATCATACAT | 55120 |
| rs769382342 | snp | C/T | 1.67503e-05 | 0.00289393 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159774 | CTTATTTCAGTGTTT[C/T]CTTCCAGACATTTTT | 55120 |
| rs769389629 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58176233 | AGATTCAATGCCATC[C/T]CCATCAAGCTACCAG | 55120 |
| rs769404124 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58203146 | CCACTAATTTTTTCC[A/C]AGACTTATCACATAT | 55120 |
| rs769425665 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165739 | CTAATGCAATTCTGC[A/G]TGCTGTTGCACTCCG | 55120 |
| rs769427855 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167657 | TAGCCAAAAACAAAA[C/T]ATCCCTGGAACTAGA | 55120 |
| rs769488483 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170142 | AGCCAGAGACAAAGG[C/T]TGGGTTACCCACAAA | 55120 |
| rs769566717 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58221009 | CGAGGTCAGGAGATC[A/G]AGACCGATCCTGGCT | 55120 |
| rs769572902 | in-del | -/CAGT | 1.65138e-05 | 0.00287343 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159532 | ATAAATACACTTCCA[-/CAGT]CAGTCAGCACGGGGA | 55120 |
| rs769622982 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184834 | TCCCCCAAAACGGGA[C/G]GAAACATCGTGAGAA | 55120 |
| rs769635718 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58201773 | CTTTTAATAAAGGAC[A/G]TCTAGTCAAAATAGG | 55120 |
| rs769636666 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58165286 | TTTACTCTTCAGTGG[A/C]ATGGTCTACTGCAAG | 55120 |
| rs769641715 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229651 | TGCCTGGAGATCTCC[C/T]GAGGACACTGAGATT | 55120 |
| rs769663888 | snp | A/C | 1.65795e-05 | 0.00287914 | splice-donor-variant, intron-variant | FANCL | GRCh38.p7 | 2:58226726 | AAAAAAAAAATTCTT[A/C]CCAAAAGCATCTTCA | 55120 |
| rs769693832 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58205166 | ACTTAGGAAATATAT[-/A]TTTTTAATATCACTA | 55120 |
| rs769762001 | snp | C/T | 3.40205e-05 | 0.00412421 | splice-acceptor-variant, intron-variant | FANCL | GRCh38.p7 | 2:58222044 | TTTAAGGCAACTTCC[C/T]GTTTAAAAGAAGAAA | 55120 |
| rs769781347 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209933 | AACCTACCAATATAT[A/G]TTGACAATCTCCCAG | 55120 |
| rs769783363 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222425 | ACCTCTAAAGAAAGG[C/T]CTGAACTCTAAGTAC | 55120 |
| rs769784879 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207742 | AAACTCTTACAAGTG[C/G]TATCAAATCAGTTTG | 55120 |
| rs769881474 | snp | A/G | 1.66123e-05 | 0.00288199 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232081 | AGTTGTAAATCTTCA[A/G]GCAACACTATCCTAA | 55120 |
| rs769884327 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58206684 | AAGTCAGAGAGGTAA[C/T]ACACTACAGAAAAAG | 55120 |
| rs769925533 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172597 | TAGCTGAGGGTCTGT[A/G]TGTTAACAGAAAAGA | 55120 |
| rs769932054 | snp | A/C | 1.77789e-05 | 0.00298146 | intron-variant | FANCL | GRCh38.p7 | 2:58198539 | GATACTCTGGGACAA[A/C]TGTACTTTTTAATTA | 55120 |
| rs769939354 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191961 | CACAAGGTCATGCAC[C/T]GGTAAAGACAGAGCC | 55120 |
| rs769973126 | snp | A/C | 1.65381e-05 | 0.00287555 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161563 | GTTGTCCACACTGAG[A/C]ATTATCACACACTTG | 55120 |
| rs769998557 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162267 | ATCTATTCAATTTTG[A/G]GAAACTATAACTGCT | 55120 |
| rs770063294 | snp | C/G | 6.64452e-05 | 0.00576352 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198646 | TCCACAAAATAATCT[C/G]GTGATTCTGCAGGAT | 55120 |
| rs770088485 | snp | C/T | 9.39717e-05 | 0.00685398 | intron-variant | FANCL | GRCh38.p7 | 2:58221897 | TACATTAAGTTAAAA[C/T]ATATAAAACAAAGGC | 55120 |
| rs770095807 | in-del | -/A/AA | 0.171762 | 0.237499 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163083 | TTACCACTTCAGATT[-/A/AA]AAAAAAAAAAAATTT | 55120 |
| rs770105669 | in-del | -/CT | | | intron-variant | FANCL | GRCh38.p7 | 2:58226439 | TTCTTAGATGTTAAA[-/CT]CTCTGCTGATAGGCC | 55120 |
| rs770131010 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58193040 | ATACTTAAGAAAAAA[C/T]TCAACAAAAATATGT | 55120 |
| rs770158440 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227344 | GAACTTTCTGTATCC[C/T]GTGGTTCCTGCCTTG | 55120 |
| rs770159346 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182084 | TCAGAGAATCTCAAA[C/T]AGGCTGAAAAAATAC | 55120 |
| rs770182004 | in-del | -/AGAATTTACCTGAGG | 0.000135199 | 0.00822078 | intron-variant | FANCL | GRCh38.p7 | 2:58198570 | CTTAAAACAAATTTA[-/AGAATTTACCTGAGG]AGAATTTACCTGAGG | 55120 |
| rs770205464 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214254 | TTTTTGGCTTTCATC[C/T]ATTATCGAAGTTAGA | 55120 |
| rs770241280 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58166516 | AAATATAGTTTCACT[-/A]AAATAATAAGTAATG | 55120 |
| rs770302859 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58222681 | CAAAACTAAAATTTT[G/T]TACAAGACACATAAA | 55120 |
| rs770309872 | snp | A/G | 1.65814e-05 | 0.00287931 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163004 | AATCACCAAAAAGTA[A/G]AAATTATATTGCCAA | 55120 |
| rs770330876 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239128 | CAACCGTGATAGTAA[C/T]AGTCGACTCAAGCAA | 55120 |
| rs770368316 | snp | A/C | 6.6788e-05 | 0.00577837 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222028 | CAGCTCTTGTCTATT[A/C]TTTAAGGCAACTTCC | 55120 |
| rs770421280 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204677 | ATCAATAATGTTACC[A/G]TACAAAAATCTAGCT | 55120 |
| rs770448326 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181638 | TTATGGGTGGAAGAA[A/G]GGATGAATAAATGGA | 55120 |
| rs770485181 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223959 | ACACTAATAATTCTT[A/G]TATCTTTAGGTATAC | 55120 |
| rs770485843 | snp | A/G | 1.65127e-05 | 0.00287334 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159546 | CACAGTCAGCACGGG[A/G]ATCACAGACTTAGAA | 55120 |
| rs770502963 | snp | A/G | 3.42847e-05 | 0.00414019 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163496 | CTGGGGTCTACCTCT[A/G]TATTTATGGAAACAT | 55120 |
| rs770528952 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180006 | TTAGAAAAATGCAAA[C/T]CAAAACCACAATGAG | 55120 |
| rs770550674 | snp | C/T | 1.74564e-05 | 0.0029543 | intron-variant | FANCL | GRCh38.p7 | 2:58226694 | TCAAGACTTGCAGTA[C/T]GGTAACAGTGTCAGA | 55120 |
| rs770602555 | in-del | -/AG | 1.6513e-05 | 0.00287336 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159558 | GGGGATCACAGACTT[-/AG]AAAGTTCAACTGGAC | 55120 |
| rs770617310 | snp | A/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160338 | GTATTTCCTGAGCCA[A/G]TAGCAGACTATTAAG | 55120 |
| rs770637324 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189161 | TGGGATGTGATGGAT[G/T]TGTTTATTATCCTGA | 55120 |
| rs770675343 | snp | A/G | 1.66713e-05 | 0.0028871 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159695 | TATTTTTTCTCTGAA[A/G]ATGATACCAAAATTC | 55120 |
| rs770688939 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197972 | AAGGAAAATGTCTGT[C/T]AAAAGTGCTTCTGCA | 55120 |
| rs770771884 | in-del | -/TG | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188327 | GTCTTGAAATCAGGT[-/TG]TGTTAGTCTTCTAAC | 55120 |
| rs770789775 | snp | C/G/T | 7.14291e-05 | 0.0059758 | intron-variant | FANCL | GRCh38.p7 | 2:58198531 | CCCCCATGGATACTC[C/G/T]GGGACAACTGTACTT | 55120 |
| rs770846942 | snp | C/T | 1.65373e-05 | 0.00287548 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161552 | TTGATGGAAAGGTTG[C/T]CCACACTGAGAATTA | 55120 |
| rs770851778 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168550 | TTGAGCTAGCTACAG[C/G]AGTTTTTTTTTTAAT | 55120 |
| rs770921798 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58211861 | AGACCACCTCAGCCT[C/G]GACCTTACTGTCCAT | 55120 |
| rs770953260 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58167859 | TTTCAACGAACTTAG[C/G]GGGTAGACATCAAAA | 55120 |
| rs770976250 | in-del | -/TAAG | 0.00015037 | 0.00866961 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159725 | CTTTTGATAATTTTT[-/TAAG]TAAGTTTCCAGCTCT | 55120 |
| rs770992806 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58189273 | GTCAATTATATCTCA[A/G]TAAAGCTATTTAAAA | 55120 |
| rs770999604 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58227475 | CGGTTTTCCCCTGGC[A/G]TCGGGTTGCTCAGCA | 55120 |
| rs771005364 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58240394 | TACACTCCTAACCTA[A/C]GGTATCCTGGTGCAA | 55120 |
| rs771016558 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58182177 | GAAATATTATCAGTA[A/G]CTGTAACTTTTTCCA | 55120 |
| rs771016640 | snp | A/C | 1.65422e-05 | 0.0028759 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159443 | GCTATACACAATTCC[A/C]AAACTCATTTTATGA | 55120 |
| rs771043484 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58164988 | ATTCACATCAGAATT[C/T]CAAAATACCCTTGAA | 55120 |
| rs771045532 | in-del | -/ATGT | | | intron-variant | FANCL | GRCh38.p7 | 2:58166170 | AGTAATGAGTACAAG[-/ATGT]ATGTACACACAACTT | 55120 |
| rs771097235 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187063 | AGCAATCCCATGACT[A/G]GGTATATACCCAAAG | 55120 |
| rs771100855 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163108 | AAATTTAATAATTGC[A/G]TGCTCTACTCTTGGT | 55120 |
| rs771136568 | snp | A/G | 1.6836e-05 | 0.00290133 | intron-variant | FANCL | GRCh38.p7 | 2:58229886 | TAATCTAAAATTTTA[A/G]TGAGACAAAATGGTT | 55120 |
| rs771138934 | in-del | -/AAA | 0.000210336 | 0.010253 | intron-variant | FANCL | GRCh38.p7 | 2:58226709 | TGGTAACAGTGTCAG[-/AAA]AAAAAAAAATTCTTA | 55120 |
| rs771218574 | snp | C/T | 1.68778e-05 | 0.00290493 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241304 | ACAGGCTCGCTTCCG[C/T]CACCGCCATGGCTCG | 55120 |
| rs771242855 | snp | C/T | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158816 | AATATCTATTCGGTC[C/T]ATACTGGTTCGTCTG | 55120 |
| rs771296573 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58215174 | CTAAAGAATGACTAG[A/G]TCCATGACATCAATG | 55120 |
| rs771342286 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207952 | TAGTTCCAGCTATTC[A/G]GGAAACTGAGGCAGA | 55120 |
| rs771345765 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58203283 | TCCAGTACAGCTTTA[C/G]ATATTAATTTTCTCT | 55120 |
| rs771351735 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220241 | GACTCTTAATCAGGG[A/G]GGCGGTAAGGAAAAC | 55120 |
| rs771356221 | in-del | -/CA | | | intron-variant | FANCL | GRCh38.p7 | 2:58224904 | AAAAGTATTTTTTCT[-/CA]GTTTTGTCCACTGAA | 55120 |
| rs771394654 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214374 | CCATATTTTATATAC[C/T]TGACTATTTCTCTTA | 55120 |
| rs771442622 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | FANCL | GRCh38.p7 | 2:58204111 | TCTGATCACAATAAC[A/G]GTTTAACGAGGCACA | 55120 |
| rs771462211 | in-del | -/TT | 3.31076e-05 | 0.0040685 | intron-variant | FANCL | GRCh38.p7 | 2:58204092 | TCATTTCACAAAGTA[-/TT]TTTTCTGATCACAAT | 55120 |
| rs771478808 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58196183 | AAGTATGCACGGATG[A/G]CCTATATACCAATTT | 55120 |
| rs771495568 | snp | A/G | 3.29701e-05 | 0.00406005 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204215 | CTGAAGCAGGTATCC[A/G]CATACACAAGTCTGG | 55120 |
| rs771560066 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58191647 | CTGTCTTTAAAGTCT[G/T]TAACATATACATAAT | 55120 |
| rs771586016 | in-del | -/AT | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160709 | TACAAAAGAAATCAC[-/AT]GTTCCCTTAGAGTAT | 55120 |
| rs771596442 | snp | A/G | 1.82737e-05 | 0.00302267 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241337 | GTCCGGAGAAACACA[A/G]AAAAGCTCTAGACCT | 55120 |
| rs771626484 | snp | A/T | 1.65633e-05 | 0.00287774 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162986 | ATGCTGTGAACTTTG[A/T]AAAATCACCAAAAAG | 55120 |
| rs771647174 | snp | A/G | 9.18632e-05 | 0.00677666 | intron-variant | FANCL | GRCh38.p7 | 2:58221904 | AGTTAAAATATATAA[A/G]ACAAAGGCATTTAAA | 55120 |
| rs771654902 | in-del | -/AGAGAACATAT | 3.37405e-05 | 0.0041072 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159808 | TAATTGGCTTTAAAA[-/AGAGAACATAT]AGAGAACATATTTTA | 55120 |
| rs771663409 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168613 | AAACTATTCACTCCC[C/G]TAGAAAGGGAGCTGA | 55120 |
| rs771669394 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225801 | CCTAATTTGTTTTAT[G/T]CAACAAATACATGGC | 55120 |
| rs771677521 | snp | A/G | 3.3134e-05 | 0.00407012 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161533 | TTACCTCATATAAGC[A/G]TATTTGATGGAAAGG | 55120 |
| rs771723328 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232505 | TGGAAGAAAAACATC[A/G]CAATATAAAATAAGG | 55120 |
| rs771742741 | in-del | -/AC | 1.66186e-05 | 0.00288254 | splice-donor-variant, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162864 | ACACTGATAAAACTT[-/AC]AGATTTTTCCAGGAT | 55120 |
| rs771755345 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240486 | GATCATCAGCAAATA[A/G]CGTCTCCGGTTTCCC | 55120 |
| rs771768209 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58179467 | TTTGACAAACATGAC[-/A]AAAACAAGCAATGGG | 55120 |
| rs771772034 | snp | A/G | 1.6531e-05 | 0.00287493 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221999 | TAGAACTGGGGAGGA[A/G]GAGGTAGTGCATACA | 55120 |
| rs771776667 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219397 | TGAGAGGGAACAAAA[C/T]CTGAGCAGAAAAATT | 55120 |
| rs771817789 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163396 | AGGCAAGGATTTTAT[G/T]ACTCTATTAAAAAAC | 55120 |
| rs771818903 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58205726 | GGCTGATAAAACAGA[A/G]AAGAAGAGAGAACAA | 55120 |
| rs771835604 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186870 | AACCAGAATGAGATA[C/T]CATCTCACACCAGTT | 55120 |
| rs771864882 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58180747 | AATAGCCACCTTCTC[-/A]ATTTTTTAACATAAG | 55120 |
| rs771906565 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224219 | TTTAATGGGACATGA[C/T]ATCTATACTTTTACT | 55120 |
| rs771934669 | snp | A/T | 1.66601e-05 | 0.00288614 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229867 | TCAGCTGCCAACTAC[A/T]TAATAATCTAAAATT | 55120 |
| rs771982403 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58225447 | AAAATTACCATTTGT[A/G]AATCCTAATGAAACA | 55120 |
| rs772025061 | snp | A/G | 4.94214e-05 | 0.00497074 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165754 | GTGCTGTTGCACTCC[A/G]TGGAGGTTTTTCTGG | 55120 |
| rs772037896 | snp | A/T | 3.43826e-05 | 0.0041461 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241313 | CTTCCGTCACCGCCA[A/T]GGCTCGAAGTCCGGA | 55120 |
| rs772044958 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243022 | ACACCTGCTTTATTT[C/T]GCAACTCGGTAATTA | 55120 |
| rs772050277 | snp | A/T | | | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229825 | TTACCTGTTGTACTA[A/T]TCGATGGTATCCACT | 55120 |
| rs772078142 | snp | A/G | 1.65045e-05 | 0.00287263 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165860 | AAACTGACTATAAAT[A/G]CTTATTAAGGAGCTC | 55120 |
| rs772093714 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231308 | CACTCCAGGTCTCAC[A/G]CTCTATTTCCACACC | 55120 |
| rs772128300 | snp | A/C | 1.65586e-05 | 0.00287733 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162980 | AAAATTATGCTGTGA[A/C]CTTTGTAAAATCACC | 55120 |
| rs772150411 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215276 | CTCTCCTCACCATTG[C/T]TATGCTTAATTTTAT | 55120 |
| rs772150996 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58228619 | TGGCTTACTAAGCCA[C/G]AAAAACTTATTATCT | 55120 |
| rs772182737 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58199028 | GTGAATCTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55120 |
| rs772224853 | snp | A/G | 1.65792e-05 | 0.00287912 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162891 | AGGATAGCACGAGCT[A/G]GAAAATCAATTTCTA | 55120 |
| rs772225810 | snp | G/T | 1.7879e-05 | 0.00298985 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159338 | AAACTATATATGTAT[G/T]TTTTCCATAGGAAAG | 55120 |
| rs772235676 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169207 | AGCTTCCAGAGAAAG[G/T]AACAGGCAGCAAAAT | 55120 |
| rs772237253 | in-del | -/A | 3.37285e-05 | 0.00410647 | intron-variant | FANCL | GRCh38.p7 | 2:58232119 | GTCTCTTCCCTGTGG[-/A]AAATATTGAAAAGGA | 55120 |
| rs772245635 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58184800 | ACACAATTCTCAGCA[A/T]CGTCCTGACCTTAAA | 55120 |
| rs772261201 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212890 | AAGGTCAACTACTAA[C/T]TCTCAATATTATTTC | 55120 |
| rs772321454 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189451 | GAAGAGTTCATACAC[C/T]CAACACTTAAAAGAA | 55120 |
| rs772348250 | snp | A/T | 1.65471e-05 | 0.00287633 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159435 | AAAAATCAGCTATAC[A/T]CAATTCCCAAACTCA | 55120 |
| rs772376654 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58174977 | ATCCCACAGAAATAC[A/G]AACTACCATCAGAGA | 55120 |
| rs772385387 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240723 | CTCCTAGAAGATATT[G/T]TAACTGTGGGTGTAC | 55120 |
| rs772393383 | snp | A/G | 3.39127e-05 | 0.00411767 | intron-variant | FANCL | GRCh38.p7 | 2:58198673 | GGATACTATTAAAAA[A/G]GCATAACATTAGACC | 55120 |
| rs772396790 | snp | C/T | 1.67351e-05 | 0.00289263 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159763 | AATGTTGTATTCTTA[C/T]TTCAGTGTTTCCTTC | 55120 |
| rs772404810 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210828 | CCAAAATGATCTCCT[C/T]TGACTCCATGTCTCA | 55120 |
| rs772415015 | in-del | -/AAAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58234146 | ATGAGACAAAGAAAC[-/AAAA]AGAGACTCACAAGAT | 55120 |
| rs772487978 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171919 | AATACTGCGCTTTTC[C/T]GACGGGTTTAAAAAA | 55120 |
| rs772569074 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236890 | TTCATAATCCTAAAG[C/G]AGTCAATTCATAAAG | 55120 |
| rs772569200 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223008 | TTAAGTATATATCAA[C/T]TTTTTTTAACCAGGA | 55120 |
| rs772652083 | snp | A/G/T | 9.89991e-05 | 0.00703497 | intron-variant | FANCL | GRCh38.p7 | 2:58204245 | GTGAGCAGAGGAGAA[A/G/T]AAAAAATGATCACAC | 55120 |
| rs772662524 | in-del | -/TATT | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241804 | TGATTATATCATATA[-/TATT]ACAGTTCTGTGGCTT | 55120 |
| rs772683953 | snp | A/G | 3.306e-05 | 0.00406558 | intron-variant | FANCL | GRCh38.p7 | 2:58204106 | TATTTTCTGATCACA[A/G]TAACAGTTTAACGAG | 55120 |
| rs772700022 | snp | A/G | 0.000115847 | 0.00760987 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241263 | TTTCGACCGGTTCTG[A/G]GGCAGAAGCAGGGGG | 55120 |
| rs772718076 | snp | A/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163397 | GGCAAGGATTTTATG[A/T]CTCTATTAAAAAACG | 55120 |
| rs772776529 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221912 | TATATAAAACAAAGG[C/T]ATTTAAAACATATTT | 55120 |
| rs772778730 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220843 | ACCTAAGTTAGCCCT[C/T]GATTTATCTTAGTAA | 55120 |
| rs772798007 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58188997 | GCCAAGGAAAAAAGA[C/T]TGGCACAGAAAAGTA | 55120 |
| rs772827443 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178696 | ATGCTCTCTCTCACC[A/T]CTCCTATTCAACACT | 55120 |
| rs772894803 | in-del | -/AG | | | intron-variant | FANCL | GRCh38.p7 | 2:58228239 | TACAATAAATATTTA[-/AG]AGTTACTATTCCATT | 55120 |
| rs772897710 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221018 | GAGATCGAGACCGAT[C/T]CTGGCTAACACGGTG | 55120 |
| rs772934507 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234380 | TATGAAAGTGAAGGA[A/T]TAAATTTAAAAAGAG | 55120 |
| rs772964961 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166918 | ACCTTCTACACATAT[A/T]TTTTTAAAAAGTGGG | 55120 |
| rs772984539 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201856 | TGGGAAAGTATGTAT[A/T]CCAGAATAAATAGAA | 55120 |
| rs773012159 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165756 | GCTGTTGCACTCCGT[A/G]GAGGTTTTTCTGGCT | 55120 |
| rs773037946 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58188016 | GCCTAGAGTTACAAA[C/T]ACTTTTCCCTGTGTT | 55120 |
| rs773040173 | in-del | -/CT | | | intron-variant | FANCL | GRCh38.p7 | 2:58231066 | ATGCCTTGCTTAAGC[-/CT]CTCTTTATTTGGCTT | 55120 |
| rs773044448 | in-del | -/AGACTT | 8.25709e-05 | 0.00642485 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159551 | CAGCACGGGGATCAC[-/AGACTT]AGACTTAGAAAGTTC | 55120 |
| rs773054616 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58195471 | ATACTTAAATACTTA[A/C]ATAGCAAAAATACCT | 55120 |
| rs773112837 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209952 | ACAATCTCCCAGTTC[A/G]CACATCAGATTTAGT | 55120 |
| rs773114848 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58222526 | AATATCCACATGCTA[A/C]TTTTTTTCACTGACT | 55120 |
| rs773117904 | snp | A/G | 1.65756e-05 | 0.00287881 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162896 | AGCACGAGCTGGAAA[A/G]TCAATTTCTAAAACA | 55120 |
| rs773164188 | snp | A/G | 3.43926e-05 | 0.0041467 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241314 | TTCCGTCACCGCCAT[A/G]GCTCGAAGTCCGGAG | 55120 |
| rs773171407 | snp | C/T | 1.77156e-05 | 0.00297615 | utr-variant-3-prime, intron-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159344 | TATATGTATTTTTTC[C/T]ATAGGAAAGCACAAG | 55120 |
| rs773195377 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241887 | TGTATTGATTAGACT[C/T]AAGTCAACACTGGAC | 55120 |
| rs773221826 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58198400 | TAGGTATTATAATCT[A/C]GAGATAACTTAAAGT | 55120 |
| rs773261619 | snp | A/G | 1.66385e-05 | 0.00288426 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161480 | AATACTTCCTATGTT[A/G]TGTTAGCGGAAAAAA | 55120 |
| rs773268744 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184943 | CAAAGGTCCGTGTTG[A/G]AGGCACACCAACCCA | 55120 |
| rs773285542 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240879 | GTGTTAAAATCGAGT[G/T]AAGGCAAAATTTACA | 55120 |
| rs773310088 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232026 | CCAAAATGCAAAAAT[A/G]CACGTTTATAACTAA | 55120 |
| rs773337207 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206701 | CACTACAGAAAAAGT[A/G]CCACGCTCAAAAATA | 55120 |
| rs773379974 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214277 | AAGTTAGAAATCTGT[A/T]CCTTTTTCTCCTACA | 55120 |
| rs773424134 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58237659 | AATTTATAAACCTCT[A/C]TCTAGATGTATCGGG | 55120 |
| rs773430569 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209662 | TATGAGTCACATAAC[A/G]TGCCTCTTTGAAATC | 55120 |
| rs773454358 | snp | A/C | 5.17487e-05 | 0.00508642 | intron-variant | FANCL | GRCh38.p7 | 2:58229782 | AATTTCTTATCTTCA[A/C]TGAAAACATAAACCT | 55120 |
| rs773518421 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229663 | TCCTGAGGACACTGA[A/G]ATTTAAAAACACACA | 55120 |
| rs773540831 | in-del | -/GAG | 1.66631e-05 | 0.00288639 | cds-indel, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198581 | TTTAAGAATTTACCT[-/GAG]GAGAATTTACCTGAG | 55120 |
| rs773541356 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218084 | GAGATATACTAAATA[A/T]GTCAAAAGAAATCAC | 55120 |
| rs773589908 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170537 | ACACATAAATGTAAA[C/T]GAGCTAAATCCCCCA | 55120 |
| rs773611035 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227350 | TCTGTATCCCGTGGT[A/T]CCTGCCTTGGTGTAC | 55120 |
| rs773655702 | snp | C/G | 3.32651e-05 | 0.00407817 | intron-variant | FANCL | GRCh38.p7 | 2:58241210 | GAAAGCAACCACTGG[C/G]CGGGTACCTGAGCCG | 55120 |
| rs773658313 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217787 | AGCTCTCAGGACAAG[C/T]GGACAAAAAAAAAAA | 55120 |
| rs773663246 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182107 | AAAAATACATCTTAA[C/T]TTCTAAGTAAAATGT | 55120 |
| rs773696049 | in-del | -/GA | | | intron-variant | FANCL | GRCh38.p7 | 2:58191739 | ATATCATTACACATG[-/GA]GAGAGACTACTTCTT | 55120 |
| rs773746576 | snp | A/G | 2.21197e-05 | 0.00332556 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161690 | CTCACTAACTTATTC[A/G]TTGTACATATTTGGG | 55120 |
| rs773762700 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193164 | TAATTTGCTGGATAA[A/G]CGTAAACCCAATTGT | 55120 |
| rs773768206 | snp | C/G | 1.65562e-05 | 0.00287712 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241264 | TTCGACCGGTTCTGG[C/G]GCAGAAGCAGGGGGC | 55120 |
| rs773780339 | snp | C/G | 1.69833e-05 | 0.00291399 | intron-variant | FANCL | GRCh38.p7 | 2:58198674 | GATACTATTAAAAAA[C/G]CATAACATTAGACCA | 55120 |
| rs773793592 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213570 | AACAGCAGCTAAATC[A/G]AAAGTCATTTATTCA | 55120 |
| rs773823387 | snp | C/T | 3.30568e-05 | 0.00406538 | intron-variant | FANCL | GRCh38.p7 | 2:58204107 | ATTTTCTGATCACAA[C/T]AACAGTTTAACGAGG | 55120 |
| rs773844602 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58210943 | CACCCGGCTGAGTTC[A/C]TGGGCTGGTGTTGAG | 55120 |
| rs773848254 | snp | A/G | 3.29919e-05 | 0.00406138 | intron-variant | FANCL | GRCh38.p7 | 2:58204232 | ATACACAAGTCTGGT[A/G]AGCAGAGGAGAATAA | 55120 |
| rs773866814 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189510 | ATAGATACATAAATG[C/T]ATATATATTGGAGAA | 55120 |
| rs773869051 | snp | A/C | 3.30814e-05 | 0.00406689 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160133 | TATGGACATTCACCA[A/C]ATATGATGTTAAAAC | 55120 |
| rs773924207 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214915 | GAGTGATTCAAAAAT[C/G]TCATATCACATCCTT | 55120 |
| rs773943899 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162574 | TATGTGAAATCTCTG[C/T]ATACAGAGGGCCGAC | 55120 |
| rs773974224 | in-del | -/CTCTTAG | 1.65121e-05 | 0.00287329 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159598 | CAATTTCCCAGTTTA[-/CTCTTAG]CTCTTAGTGAAGAGA | 55120 |
| rs774019849 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58201542 | ATACAAATTGCAGCA[A/G]AGAAAGAGTGCCCAC | 55120 |
| rs774033309 | snp | C/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159306 | TAAATACTTGGATAA[C/G]TCACGTCTAACAAAC | 55120 |
| rs774035220 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58180525 | GAACACATGGACACA[A/G]GGAGGGAAATATCAC | 55120 |
| rs774047558 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58167007 | TCACGAGGTCAAGAG[A/C]TAGAGACCATCCTGG | 55120 |
| rs774067966 | in-del | -/A | 3.35587e-05 | 0.00409613 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159789 | CTTCCAGACATTTTT[-/A]AAGGTAATTGGCTTT | 55120 |
| rs774102616 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179592 | AATTAACACAATATG[C/G]ATTAAAGACTTAAAC | 55120 |
| rs774109214 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203398 | TTGATTGATTGACTC[C/T]AAGAATAATTAAAAA | 55120 |
| rs774118062 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185034 | AAAAAAGAGGCACAG[C/G]CCAAACAAGAGAAAC | 55120 |
| rs774120064 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242023 | TCTAACTCAGGAATG[C/T]TATCCATCCCATCTT | 55120 |
| rs774130265 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169110 | TCTGCTAAGGGACAG[A/G]CTGCCTCCTCAAGCA | 55120 |
| rs774130469 | snp | A/T | 0.000118152 | 0.0076852 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159811 | ATTGGCTTTAAAAAG[A/T]GAACATATTTTAACA | 55120 |
| rs774183899 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185986 | AAACTAGGTACAAGT[A/G]CAGCTAAGAAGTCAG | 55120 |
| rs774247054 | snp | A/T | 1.69112e-05 | 0.0029078 | intron-variant | FANCL | GRCh38.p7 | 2:58198667 | TCTGCAGGATACTAT[A/T]AAAAAAGCATAACAT | 55120 |
| rs774253715 | in-del | -/CACCA | | | intron-variant | FANCL | GRCh38.p7 | 2:58174345 | ATACATTTTTCTCAG[-/CACCA]CACCACACCACACCT | 55120 |
| rs774257449 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196999 | AAAAAAAGAAAGCTA[C/T]AAAATTTATGCATAA | 55120 |
| rs774347184 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182281 | TTAATTGATATTAGT[C/T]CAATACAGCCTTTAT | 55120 |
| rs774352583 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216484 | TCCAAATTAAGCCAG[C/T]TTCCTCATTTATCTC | 55120 |
| rs774358564 | snp | A/C | 1.64895e-05 | 0.00287132 | intron-variant | FANCL | GRCh38.p7 | 2:58165679 | TATTTTCATAATACA[A/C]AATAAAACACCTAAA | 55120 |
| rs774358700 | snp | C/T | 1.73534e-05 | 0.00294558 | intron-variant | FANCL | GRCh38.p7 | 2:58229774 | AATTTAGTAATTTCT[C/T]ATCTTCACTGAAAAC | 55120 |
| rs774375375 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58165033 | AGAAAAAAAGAAATG[G/T]GTATCTTAAAACTAG | 55120 |
| rs774411712 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165748 | TTCTGCGTGCTGTTG[A/C]ACTCCGTGGAGGTTT | 55120 |
| rs774416980 | snp | A/G | 1.99958e-05 | 0.00316188 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161671 | TTATAAAAAGCGTAT[A/G]TGTCTCACTAACTTA | 55120 |
| rs774425575 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167725 | CCTAAAAGCCATTAT[A/T]CGATTTTACTAGCTA | 55120 |
| rs774453026 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239363 | CTGCCAAAAATGCAT[G/T]AGCTGAATTTAATAG | 55120 |
| rs774479802 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227485 | CTGGCGTCGGGTTGC[C/T]CAGCAGCCCAGGCTC | 55120 |
| rs774518191 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194663 | TGAGCCAGAATACAC[C/T]GGCTGTTGCTGATCA | 55120 |
| rs774596605 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58238606 | GAAAGAGAAAATCTG[A/G]TAATAGAGACAACAC | 55120 |
| rs774632268 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234656 | GCCACATGATAAAAG[C/T]GATTCACAATGATCA | 55120 |
| rs774650533 | in-del | -/G | 1.64866e-05 | 0.00287106 | frameshift-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204159 | TGAGAGTGATTAAAT[-/G]CTCTCTACCAGAAGC | 55120 |
| rs774687988 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212434 | CACAGGGGATACAGA[A/G]CCAAACCATATCATA | 55120 |
| rs774737156 | snp | A/G | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158827 | GGTCTATACTGGTTC[A/G]TCTGTATAGCTTTCC | 55120 |
| rs774751115 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193519 | TATACTTTTTCTACC[A/G]TATCACATAATCTCA | 55120 |
| rs774777844 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58210203 | GACACACCCAAGACT[C/T]GGCAATTTACAAAAG | 55120 |
| rs774787165 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58230159 | CCACTGAAGTAGATT[A/C]TTTTCCAAGATAGGT | 55120 |
| rs774791078 | snp | A/G | 1.6588e-05 | 0.00287988 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159667 | GTCCTTTTGATGTTA[A/G]TATTTCTTGCTTTAT | 55120 |
| rs774840155 | snp | C/T | 1.66366e-05 | 0.0028841 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232092 | TTCAGGCAACACTAT[C/T]CTAAGGTGGAAGTCT | 55120 |
| rs774870650 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170299 | CTAACCTTCAGGAGT[A/G]AAGGAGAAATAAAAT | 55120 |
| rs774922003 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183177 | ATAAGGTTACTAAAA[A/T]ATATTTAAAATAAAA | 55120 |
| rs774940458 | in-del | -/AATTTCATTTGCACAATA | 1.73426e-05 | 0.00294466 | intron-variant | FANCL | GRCh38.p7 | 2:58226807 | AAAATATTTCCAATT[-/AATTTCATTTGCACAATA]AATATTCTATCCACT | 55120 |
| rs774989597 | snp | C/T | 1.65471e-05 | 0.00287633 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160113 | ATTTGCTTACCTTAC[C/T]ACAATATGGACATTC | 55120 |
| rs775001589 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198380 | ACATGGCAAATGCAT[C/T]GTATTAGGTATTATA | 55120 |
| rs775008073 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180123 | TTTGACACTGTTGGT[C/T]GAAGTGTAAATTAGT | 55120 |
| rs775011832 | snp | C/G | 6.06594e-05 | 0.00550691 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163555 | CTTTTAGAAGTAGAA[C/G]AGCTCATCAAACAAC | 55120 |
| rs775024946 | in-del | -/TG | | | intron-variant | FANCL | GRCh38.p7 | 2:58227666 | ACGTCCAGCCACTTG[-/TG]TGTGTGTGTGCCTGC | 55120 |
| rs775029963 | in-del | -/TC | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188467 | TTTTTTGAGATAGGG[-/TC]TCTCTGTCACCCAGG | 55120 |
| rs775030893 | in-del | -/AGAAC | 3.37547e-05 | 0.00410807 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159810 | ATTGGCTTTAAAAAG[-/AGAAC]AGAACATATTTTAAC | 55120 |
| rs775066921 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58193535 | TATCACATAATCTCA[A/G]TAATAAATTTTCTTT | 55120 |
| rs775079349 | in-del | -/TTTATATATATATTTATATATTT | | | intron-variant | FANCL | GRCh38.p7 | 2:58217144 | ATTTTTATATATAGA[-/TTTATATATATATTTATATATTT]TATATATATATATAT | 55120 |
| rs775146550 | in-del | -/CAT | 1.65378e-05 | 0.00287552 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159639 | TGTTTATTATTATCG[-/CAT]CATCATACCTGTCCT | 55120 |
| rs775180337 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168634 | AGGGAGCTGATGCCA[C/G]GGCGCCAAGTGGTCT | 55120 |
| rs775202487 | snp | A/G | 1.70371e-05 | 0.0029186 | intron-variant | FANCL | GRCh38.p7 | 2:58222045 | TTAAGGCAACTTCCT[A/G]TTTAAAAGAAGAAAA | 55120 |
| rs775213684 | in-del | -/TTCT | | | intron-variant | FANCL | GRCh38.p7 | 2:58203983 | AACGTGGTGAATAAA[-/TTCT]TTGAGGCTTTCCAAA | 55120 |
| rs775231756 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240640 | ACATGTGTTAGTATG[G/T]GTAATAAACTCCATA | 55120 |
| rs775257540 | snp | A/T | 1.72448e-05 | 0.00293634 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163502 | TCTACCTCTATATTT[A/T]TGGAAACATTATTAC | 55120 |
| rs775260063 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58224376 | CTTTACCTTTTTAAG[G/T]TTATTACATTAAGGC | 55120 |
| rs775310385 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172872 | CAAACCAAAGGCGAA[A/G]AAGCTGAAAACTTTG | 55120 |
| rs775321888 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238242 | TTCTTCCAATGTGAC[C/T]CAGGGAAGCCAAAAG | 55120 |
| rs775372392 | snp | A/T | 1.66233e-05 | 0.00288295 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232087 | AAATCTTCAGGCAAC[A/T]CTATCCTAAGGTGGA | 55120 |
| rs775449389 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58186881 | GATATCATCTCACAC[C/T]AGTTAGAATGGCAAT | 55120 |
| rs775486124 | snp | A/G | 6.64949e-05 | 0.00576568 | intron-variant | FANCL | GRCh38.p7 | 2:58165897 | AAAAATGAAAGTTGA[A/G]TAAGTTATATGGTAC | 55120 |
| rs775554655 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58189535 | GGAGAAGAGGGAAAG[A/G]TATATGTGAGAACTA | 55120 |
| rs775616604 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215369 | TCTCATGAATAAATA[C/T]CAACCAGTCCTCAAT | 55120 |
| rs775664760 | snp | C/G | 1.66299e-05 | 0.00288352 | splice-donor-variant, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163028 | TTGCCAAGGTACCTA[C/G]CACAAATGTATGTTC | 55120 |
| rs775691874 | in-del | -/AG | 1.71202e-05 | 0.00292572 | intron-variant | FANCL | GRCh38.p7 | 2:58241177 | CGCAGCTACGCTGCA[-/AG]AGAGGCTCTCTTAGC | 55120 |
| rs775708061 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171297 | TAACAAAATTAAGGC[A/G]GAAATAAATAAGTTT | 55120 |
| rs775779594 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223007 | TTAAGTATATATCAA[-/T]TTTTTTTTAACCAGG | 55120 |
| rs775812458 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58183352 | ATTAAGTATATGGGT[A/G]TAGGTCTGAATTCTC | 55120 |
| rs775820902 | in-del | -/AATT | | | intron-variant | FANCL | GRCh38.p7 | 2:58167987 | AAATTGAAAAAAATA[-/AATT]ATTTCTAAATATTAC | 55120 |
| rs775879116 | snp | A/C/T | 4.68782e-05 | 0.00484121 | intron-variant | FANCL | GRCh38.p7 | 2:58221899 | CATTAAGTTAAAATA[A/C/T]ATAAAACAAAGGCAT | 55120 |
| rs775890254 | in-del | -/ATTTAAAACATA | 2.07568e-05 | 0.00322149 | intron-variant | FANCL | GRCh38.p7 | 2:58221913 | ATATAAAACAAAGGC[-/ATTTAAAACATA]TTTTAAAACAGACAT | 55120 |
| rs775899762 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230367 | CTGGCTGGAGTGCAG[C/T]AGAATAGCTGACTGC | 55120 |
| rs775926507 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58173142 | TGGCACCATGTGAAA[A/C]GACCAAACCTACGTC | 55120 |
| rs775956248 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203578 | TTGTGCCAATAAAAT[C/T]TGTGATTATAGATCA | 55120 |
| rs776013150 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204748 | TGCTGTATAAGCACA[A/G]GTACAGCCTGGTCTC | 55120 |
| rs776040668 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58175705 | CAAAAACTTGAAGCA[A/T]TCCCTTTGAAAACCA | 55120 |
| rs776061969 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223082 | TACAAAACAGCACTT[C/T]AAAACCAAAACTATT | 55120 |
| rs776063926 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58236982 | AAACTGATAGAAATT[A/G]AATAGAAATTGAAAA | 55120 |
| rs776093478 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | FANCL | GRCh38.p7 | 2:58229908 | AAAATGGTTTATTCA[C/T]TGTTCAGAATTAAAA | 55120 |
| rs776125101 | snp | C/G | 1.65153e-05 | 0.00287356 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159551 | TCAGCACGGGGATCA[C/G]AGACTTAGAAAGTTC | 55120 |
| rs776150803 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186903 | AATGGCAATCATTAA[A/G]AAGTCAGGAAACAAC | 55120 |
| rs776153043 | in-del | -/TCTTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58214385 | ATACTTGACTATTTC[-/TCTTA]TAACTCTCAAGAATC | 55120 |
| rs776153655 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236009 | AGTGACCTAAATGCA[C/T]GTATTTGGAGTGCCC | 55120 |
| rs776189946 | snp | C/G/T | 5.14296e-05 | 0.00507076 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163497 | TGGGGTCTACCTCTA[C/G/T]ATTTATGGAAACATT | 55120 |
| rs776241464 | snp | C/G | 1.95372e-05 | 0.00312541 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163546 | AGATTAAATCTTTTA[C/G]AAGTAGAACAGCTCA | 55120 |
| rs776270094 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231580 | TATTTAGAGGCAGAA[C/T]TGAGATTTGGGGTGG | 55120 |
| rs776291778 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58169351 | CAAACAGAAAGCAAT[A/C]GCATCAACATCAACA | 55120 |
| rs776298788 | snp | A/G | 1.65353e-05 | 0.00287531 | stop-gained, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161560 | AAGGTTGTCCACACT[A/G]AGAATTATCACACAC | 55120 |
| rs776337696 | snp | C/T | 1.87278e-05 | 0.00305999 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241345 | AAACACAGAAAAGCT[C/T]TAGACCTGCTGGGTC | 55120 |
| rs776377992 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58196595 | ATAAGGCACTGAGCA[C/T]GTGGATATAAAATTT | 55120 |
| rs776383671 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58178604 | GTAACAGCTATTTAT[G/T]ACAAACCCACAGTCA | 55120 |
| rs776387216 | snp | A/C | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243102 | CAAAAGTGGGATCAA[A/C]ACAAAGATTAAGAGA | 55120 |
| rs776399646 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166761 | TGATACACCCTAAGA[G/T]GAAAAGAAACTAGCC | 55120 |
| rs776404841 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213352 | AGGTCCTGAAACCCA[A/G]TTTTATCAGTGTATG | 55120 |
| rs776423906 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209645 | CTTTACACTAGGAAC[G/T]ATATGAGTCACATAA | 55120 |
| rs776448800 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58165512 | GTTACCTCCATTGGA[C/T]CATCACCTTTTATAA | 55120 |
| rs776455775 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58200246 | GCCATATTTAAAAAT[A/C]GTGATTATCTCAAAG | 55120 |
| rs776459462 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58208162 | ATCATTCAAATAATG[A/T]TTTAGGAAACAATCA | 55120 |
| rs776463455 | snp | A/G | 1.77439e-05 | 0.00297853 | intron-variant | FANCL | GRCh38.p7 | 2:58221929 | TTTAAAACATATTTT[A/G]AAACAGACATACTTA | 55120 |
| rs776509263 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204851 | AATATTCTAAACATA[C/T]AGCACAAGCACAACT | 55120 |
| rs776536382 | snp | A/G | 1.65318e-05 | 0.002875 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159457 | CCAAACTCATTTTAT[A/G]AGCCTCATCAAGATT | 55120 |
| rs776572988 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220626 | GGTAATGGTATAAAA[C/T]ATATTAAAGGACATA | 55120 |
| rs776623930 | snp | A/G | 1.67371e-05 | 0.0028928 | intron-variant | FANCL | GRCh38.p7 | 2:58229805 | ATAAACCTTTTAAAA[A/G]GGACTTACCTGTTGT | 55120 |
| rs776681755 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225885 | CTTATAAGTCTTATA[G/T]AAGGCTTAAGAGACT | 55120 |
| rs776732887 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58181150 | CTGGTAACAGTCCAG[-/A]ATGTTTGTCAACAGG | 55120 |
| rs776744907 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58216348 | AATATCATCTGGGGC[C/T]TCTAAACTATTTTAT | 55120 |
| rs776750454 | snp | A/T | 3.36734e-05 | 0.00410312 | intron-variant | FANCL | GRCh38.p7 | 2:58229887 | AATCTAAAATTTTAA[A/T]GAGACAAAATGGTTT | 55120 |
| rs776879651 | snp | G/T | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165872 | AATGCTTATTAAGGA[G/T]CTCTGTGAAAAAAAT | 55120 |
| rs776891156 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171970 | TCCCGCTTGGAGAGT[C/G]CTACGCCCACGGAGC | 55120 |
| rs776893356 | snp | C/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160988 | ACAGGAATGAAAGTA[C/G]ACTTCACATACAGTA | 55120 |
| rs776927609 | in-del | -/GAGAAGCGTCAGCATGATTACAAATTACAGATACTCCAAATGT | 1.67399e-05 | 0.00289304 | frameshift-variant, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163059 | TGCTCAGCTTAATTC[lengthTooLong]CCAGGGGTTTTACCA | 55120 |
| rs776928216 | in-del | -/AC | 9.01104e-05 | 0.00671171 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241332 | TCGAAGTCCGGAGAA[-/AC]ACAGAAAAGCTCTAG | 55120 |
| rs776946309 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171541 | AGCAGAACTGAAGGA[A/G]ATAGAGACACGAAAA | 55120 |
| rs776977788 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169440 | AGATAAATCCACGAC[A/G]ATGAGGAAAAACTCG | 55120 |
| rs777029078 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181216 | TGGACTATTACTCAG[A/G]AATAAAAAGGAATGA | 55120 |
| rs777034581 | in-del | -/AAAT | 1.71173e-05 | 0.00292547 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159846 | TGTGGACACTCTAAA[-/AAAT]AAATAAAATTGCTTT | 55120 |
| rs777055093 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58200104 | GTGGTCTACTTCTGG[-/A]AAAAAAAAAAAAGAA | 55120 |
| rs777059394 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190134 | CTTTCTACAGGTATA[A/T]CTGTAACTGAATTTG | 55120 |
| rs777075089 | snp | A/G | 4.95397e-05 | 0.00497668 | intron-variant | FANCL | GRCh38.p7 | 2:58204117 | CACAATAACAGTTTA[A/G]CGAGGCACATACCTT | 55120 |
| rs777076199 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214594 | GCTCCCTGCAGCCTC[C/G]ACCTACCCAGGCTCA | 55120 |
| rs777111103 | in-del | -/TGTT | 1.65693e-05 | 0.00287826 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159661 | TACCTGTCCTTTTGA[-/TGTT]TGTTAGTATTTCTTG | 55120 |
| rs777157461 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58237451 | AAATGTGTGTGATAT[A/G]GCTAAACCAGTATTC | 55120 |
| rs777166171 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234731 | AAAGTCCAGAGTCTC[C/T]AGGTAAAAGATCAAA | 55120 |
| rs777175455 | snp | A/T | 9.98934e-05 | 0.00706659 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162849 | GTCTGGAATATCAAA[A/T]CACTGATAAAACTTA | 55120 |
| rs777182078 | snp | C/T | | | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158856 | CCAAGAGACATAACA[C/T]TATAGCTACCCCTGA | 55120 |
| rs777183898 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58206364 | AAACATGAATATTTC[A/G]AAGTATTTGTCTCAA | 55120 |
| rs777200025 | snp | C/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204222 | AGGTATCCGCATACA[C/G]AAGTCTGGTGAGCAG | 55120 |
| rs777205908 | snp | A/G | 1.65638e-05 | 0.00287778 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162911 | ATCAATTTCTAAAAC[A/G]TCTTTCAAATTTTGT | 55120 |
| rs777206203 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58212158 | TTACAGTTCCACATG[A/G]CTGGGGAAGCCTCAC | 55120 |
| rs777219755 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58235541 | ATTTAACTGTAGCTC[A/C]CAACAAATCTCAAGA | 55120 |
| rs777241643 | snp | C/T | 1.65965e-05 | 0.00288062 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161519 | AATATTTTTATTTTT[C/T]ACCTCATATAAGCAT | 55120 |
| rs777259158 | snp | C/G | 8.28727e-05 | 0.00643657 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162995 | ACTTTGTAAAATCAC[C/G]AAAAAGTAAAAATTA | 55120 |
| rs777291161 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58169869 | AAAAAGAATGAGAAG[C/G]AATGAACAAAGCCTC | 55120 |
| rs777292945 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171821 | TGCCTCCCTCGGGAA[A/G]TGCAAAGGGTCAGGG | 55120 |
| rs777343898 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170821 | TGCAACAAGGAGAGC[C/T]AACAATCCTAAATGT | 55120 |
| rs777360910 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190751 | GCCAAGGAACTAACA[A/G]TGACATCATTTAATT | 55120 |
| rs777378352 | snp | C/T | 1.65392e-05 | 0.00287564 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161549 | TATTTGATGGAAAGG[C/T]TGTCCACACTGAGAA | 55120 |
| rs777383038 | snp | A/G | 3.30639e-05 | 0.00406581 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222000 | AGAACTGGGGAGGAG[A/G]AGGTAGTGCATACAG | 55120 |
| rs777389059 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58229383 | AGCAGCCTTTAATTT[A/G]TCTCCCCTCATTATG | 55120 |
| rs777424997 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58190329 | AAACATAGTCACCTC[A/T]TGTGTAGCCATCACA | 55120 |
| rs777455228 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203131 | AATGAGATTTCCATC[C/T]CACTAATTTTTTCCA | 55120 |
| rs777465123 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215117 | ACATTAAGCATCTGA[A/T]GATAAGTCAAAATAA | 55120 |
| rs777484681 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58211783 | ATACCACCAGCCTCT[C/T]TGCTAAAACATAACA | 55120 |
| rs777548616 | snp | C/G | 1.70377e-05 | 0.00291865 | intron-variant | FANCL | GRCh38.p7 | 2:58232138 | TATTGAAAAGGATCA[C/G]TCAAATTTTTATCTT | 55120 |
| rs777569280 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168859 | TGGGCAGAGCTCACC[A/G]CAGCTCAGCAAAGCC | 55120 |
| rs777575772 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210712 | GGGGTATAGGCATTC[A/G]ATAAATACAGCCATT | 55120 |
| rs777591674 | in-del | -/ATTTTTT | 3.34093e-05 | 0.004087 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159720 | AAATTCCTTTTGATA[-/ATTTTTT]AAGTTTCCAGCTCTT | 55120 |
| rs777650949 | snp | A/G | 1.65228e-05 | 0.00287422 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159629 | CAAACGCAGATGTTT[A/G]TTATTATCGCATCAT | 55120 |
| rs777659238 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58167801 | GGGGAAAAGAAAGAT[A/C]AAAAATGTGACAAGT | 55120 |
| rs777689729 | snp | A/T | 3.32674e-05 | 0.0040783 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232061 | CATATCACCTTGCAT[A/T]CTTCAGTTGTAAATC | 55120 |
| rs777712172 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179966 | GCCAACAAACATATG[A/G]AAAAAAGCTCATCAT | 55120 |
| rs777743179 | snp | C/T | 0.000136958 | 0.00827408 | intron-variant | FANCL | GRCh38.p7 | 2:58194291 | GGACAAAAGGAATTT[C/T]GTTTTTTTATAATCA | 55120 |
| rs777834284 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232419 | TGCTAACCAGGCCCA[C/T]AGAAGAAATTTCAGT | 55120 |
| rs777874853 | snp | A/C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58174694 | GAAAGCAGCAAAGAT[A/C/T]CAAAATTGACACCCT | 55120 |
| rs777915253 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58233509 | CCCACATATCATACC[-/A]AAAAGCTACATCAAT | 55120 |
| rs777947589 | snp | C/T | | | stop-gained, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160178 | AGTAGTCCTCTCAGC[C/T]ACTGCAAATTTTAAA | 55120 |
| rs777949859 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204211 | GGTACTGAAGCAGGT[A/G]TCCGCATACACAAGT | 55120 |
| rs777951844 | snp | C/G/T | 3.55652e-05 | 0.00421682 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241325 | CCATGGCTCGAAGTC[C/G/T]GGAGAAACACAGAAA | 55120 |
| rs777954960 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58236474 | TAGTTAAAAAAAAAA[-/C]CACACACACACACAG | 55120 |
| rs778001179 | snp | C/G | 1.65408e-05 | 0.00287578 | intron-variant | FANCL | GRCh38.p7 | 2:58204270 | TCACACCGGGGAGAG[C/G]TGGAGAGGGGAACTG | 55120 |
| rs778005017 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231300 | CACATCTGCACTCCA[C/G]GTCTCACACTCTATT | 55120 |
| rs778023041 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58187346 | CGCATGTTCTCACTC[A/G]TAGGTGAGAACTGAA | 55120 |
| rs778025797 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220180 | AATTTTTATCAAGAC[C/G]AGGATTTAAATAACT | 55120 |
| rs778042020 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58182960 | TTAGCATTTGTAATA[C/T]GGAAATAGTGTTAAT | 55120 |
| rs778049860 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58197868 | TATTATGTAATCAAT[A/G]TCAAAAGTTTTAGCA | 55120 |
| rs778068203 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165736 | TACCTAATGCAATTC[C/T]GCGTGCTGTTGCACT | 55120 |
| rs778070796 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166102 | AGAAAGAATGGTTTT[A/T]TAAAAATCATAATTT | 55120 |
| rs778085502 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58233741 | ACTAAGTAAGTGTAA[A/G]AAAAAATAGTAACAA | 55120 |
| rs778127243 | snp | A/C | 1.65652e-05 | 0.0028779 | intron-variant, downstream-variant-500B, stop-gained, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160094 | TTATGAGATGTGATT[A/C]ACAATTTGCTTACCT | 55120 |
| rs778155183 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195801 | TGCAAAGAATATGCA[C/T]TGCTGAATGGGAATA | 55120 |
| rs778189346 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58194335 | CTTAAAATCTGACAT[G/T]TAGGCATTCTACAGT | 55120 |
| rs778252009 | snp | G/T | 3.31802e-05 | 0.00407296 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160197 | GCAAATTTTAAAAGA[G/T]AAAGGAGAAGCGTCA | 55120 |
| rs778297632 | snp | C/T | 1.66252e-05 | 0.00288311 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160216 | GGAGAAGCGTCAGCA[C/T]GATTACAAATTACAG | 55120 |
| rs778392579 | snp | C/G | 1.68519e-05 | 0.0029027 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241302 | CAACAGGCTCGCTTC[C/G]GTCACCGCCATGGCT | 55120 |
| rs778410523 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240178 | TCTACAAGAGAATCA[C/T]ATTTTCAGCTAGGTA | 55120 |
| rs778413514 | snp | C/G | 8.28027e-05 | 0.00643386 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162985 | TATGCTGTGAACTTT[C/G]TAAAATCACCAAAAA | 55120 |
| rs778417028 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209195 | AACTTTTTAATAAGG[A/G]ATATGAAAGCTTTAT | 55120 |
| rs778466592 | snp | C/T | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161750 | TACAGTGTTTAATGA[C/T]GACATCAGGATAATT | 55120 |
| rs778470169 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210567 | CCCAACAGGCCCCCC[A/G]AAGTCTTAACTTATT | 55120 |
| rs778500880 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58238045 | CAATAGCTATGTGAA[C/T]GAGCAATCTTGGAAG | 55120 |
| rs778525938 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217623 | TCCTAATAACAAAAG[G/T]GAAAACCAACAAGGA | 55120 |
| rs778527521 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165840 | AGTGATTCTATTGCT[C/G]CCAAAAACTGACTAT | 55120 |
| rs778558061 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58180825 | TTGTGTGTGTGTGCC[C/T]ATTTGTAATGTGCAA | 55120 |
| rs778580417 | snp | C/T | 0.000410874 | 0.0143272 | intron-variant | FANCL | GRCh38.p7 | 2:58194212 | TTCACCAAGCCTGCA[C/T]TTAGTGGCACACTTA | 55120 |
| rs778620783 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58204709 | GTATTTGTTCATATA[C/G]TCAAATTGATCCTCT | 55120 |
| rs778622855 | snp | C/T | 1.65737e-05 | 0.00287864 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161526 | TTATTTTTTACCTCA[C/T]ATAAGCATATTTGAT | 55120 |
| rs778628106 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58199866 | TTTTTTCAGCCTCTT[A/G]TTTTTCAGTACTCTG | 55120 |
| rs778693777 | snp | A/G | 1.6552e-05 | 0.00287676 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159419 | TAAACAGTTTCCCAC[A/G]AAAAATCAGCTATAC | 55120 |
| rs778782244 | snp | A/G | 3.48566e-05 | 0.00417457 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163088 | CACTTCAGATTAAAA[A/G]AAAAAAATTTAATAA | 55120 |
| rs778796508 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170218 | AAGCCAGAAGAGAGT[-/G]GGGGGCCAATATTTA | 55120 |
| rs778820117 | snp | A/C | 1.65141e-05 | 0.00287346 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159522 | TCCATCTTGGTATAA[A/C]TACACTTCCACAGTC | 55120 |
| rs778894850 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58218471 | ATCACTATAGATCCT[-/A]AAAATCATTTTTTAA | 55120 |
| rs778926534 | in-del | -/T | 1.65625e-05 | 0.00287766 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159411 | GAATGAAGTAAACAG[-/T]TTCCCACAAAAAATC | 55120 |
| rs778933999 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168577 | TAATACCCCAGTGGC[A/G]CCTGCAACACCAGCA | 55120 |
| rs778940762 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58167336 | TGTAAGTTTAGGTGA[A/C]AGAATCCAGAAATCA | 55120 |
| rs778948144 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213003 | AATGTCTAATCCTAT[A/G]GAGTTGATTAGAAAT | 55120 |
| rs778972805 | snp | C/G/T | 3.32675e-05 | 0.00407834 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229863 | GTTCTCAGCTGCCAA[C/G/T]TACATAATAATCTAA | 55120 |
| rs778982249 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58220544 | CCTCTAGAAACAAAT[G/T]TACATGGGAACAATT | 55120 |
| rs778990486 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204201 | TTAACTTGATGGTAC[C/T]GAAGCAGGTATCCGC | 55120 |
| rs778992712 | in-del | -/TG | | | intron-variant | FANCL | GRCh38.p7 | 2:58233157 | CACTAAAAGGTATTA[-/TG]TAGTAACTTTAACCT | 55120 |
| rs778995956 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58179764 | AGCTCCTTCACAGCA[A/G]AAGAAACTATCATTA | 55120 |
| rs779011743 | in-del | -/G | 1.83954e-05 | 0.00303271 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161647 | TAAAATCCTTCAAAA[-/G]AAAAATATTTATAAA | 55120 |
| rs779043657 | snp | C/T | 1.65573e-05 | 0.00287721 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162977 | AAAAAAATTATGCTG[C/T]GAACTTTGTAAAATC | 55120 |
| rs779047274 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58179153 | GTGAAAATGGCCATA[A/C]TGCCCTAAGTAATTT | 55120 |
| rs779054490 | snp | C/T | 1.65592e-05 | 0.00287738 | intron-variant | FANCL | GRCh38.p7 | 2:58204091 | GTTCATTTCACAAAG[C/T]ATTTTCTGATCACAA | 55120 |
| rs779056711 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58189308 | AGTCATTCTGATTTA[C/T]GAACAGTAATGGATC | 55120 |
| rs779081355 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58210637 | TAAGACAAGGCAAGT[C/G]TCTTCCACCGATGAG | 55120 |
| rs779117531 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240515 | CCATACCTTGATTTC[C/T]TCAACTAGAAAATGG | 55120 |
| rs779171792 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233951 | TCTTATACGAGTAAA[C/T]AAAAAAACAACTCCT | 55120 |
| rs779180336 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58174877 | AAAGGATCAACAAAA[C/T]TGATAGACCGCTAGC | 55120 |
| rs779182717 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58230855 | TTTTTTCTCCTTAAT[A/G]AATTAACTTGCTCAA | 55120 |
| rs779188725 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216051 | TAACAAAAAGTGATA[A/G]AGCTTTGTCAAAAAT | 55120 |
| rs779198812 | snp | C/G | 1.75145e-05 | 0.00295921 | intron-variant | FANCL | GRCh38.p7 | 2:58226685 | AAAAAGAAATCAAGA[C/G]TTGCAGTATGGTAAC | 55120 |
| rs779229028 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222163 | AGTGCCTGTTTTTTT[A/G]CGGAAATCTGGCTGA | 55120 |
| rs779236147 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184780 | ATGGTATGAGAAGGA[A/G]AAGAACACAATTCTC | 55120 |
| rs779275069 | snp | G/T | 3.34549e-05 | 0.00408978 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159757 | CACCGAAATGTTGTA[G/T]TCTTATTTCAGTGTT | 55120 |
| rs779312251 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58209629 | CAACTTGATACACCT[A/T]CTTTACACTAGGAAC | 55120 |
| rs779321242 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171912 | CCACCCCAATACTGC[A/G]CTTTTCCGACGGGTT | 55120 |
| rs779368697 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228545 | GCCATACACATTCAC[C/T]TACCTCTTGTCTATG | 55120 |
| rs779376983 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant | FANCL | GRCh38.p7 | 2:58165718 | CTTAATCCTCCTTGT[C/T]CCTACCTAATGCAAT | 55120 |
| rs779427183 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229636 | TTTCAACACAAAGGC[C/T]GCCTGGAGATCTCCT | 55120 |
| rs779439089 | snp | A/G/T | 3.2948e-05 | 0.00405871 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165744 | GCAATTCTGCGTGCT[A/G/T]TTGCACTCCGTGGAG | 55120 |
| rs779444170 | in-del | -/GTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58204694 | ACAAAAATCTAGCTG[-/GTA]TTTGTTCATATACTC | 55120 |
| rs779490254 | in-del | -/A | 1.6507e-05 | 0.00287284 | frameshift-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165863 | TGACTATAAATGCTT[-/A]ATTAAGGAGCTCTGT | 55120 |
| rs779531933 | in-del | -/AGTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58168081 | TTAAAATCAAAGTTC[-/AGTA]AGTATTTTGCAGGGA | 55120 |
| rs779544327 | in-del | -/TT | 4.98732e-05 | 0.00499341 | frameshift-variant, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58222019 | TAGTGCATACAGCTC[-/TT]GTCTATTCTTTAAGG | 55120 |
| rs779544653 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58220326 | AGGAATGGCTAACCT[A/G]TCTCTGCACATAGGT | 55120 |
| rs779559043 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166555 | GACTTTAAAAATCAG[G/T]TTTTAAACAAAGGAG | 55120 |
| rs779560793 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58195899 | CTGAAATCCAGCATT[G/T]TCACTTCTAGGAAAA | 55120 |
| rs779587713 | in-del | -/C | 4.98525e-05 | 0.00499237 | splice-donor-variant, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162865 | CACTGATAAAACTTA[-/C]AGATTTTTCCAGGAT | 55120 |
| rs779602148 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58182694 | TCCTCACTTACATCA[C/G]ATCAGGTTATACAAA | 55120 |
| rs779656622 | in-del | -/ATAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58184196 | ATACATCCATTAAAT[-/ATAA]ATGTCTATTTATATG | 55120 |
| rs779666299 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58202790 | TCAACTTGGATTAAA[A/C]TCTTGTAGGTATAGT | 55120 |
| rs779718489 | snp | C/T | 3.31708e-05 | 0.00407238 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229840 | TTCGATGGTATCCAC[C/T]AAGTATTGTTCTCAG | 55120 |
| rs779745877 | snp | A/G | 3.29603e-05 | 0.00405944 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165826 | CCCAGAATGCCTTTA[A/G]TGATTCTATTGCTGC | 55120 |
| rs779753992 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58191743 | CATTACACATGGAGA[C/G]AGACTACTTCTTTGC | 55120 |
| rs779777610 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187767 | TTGAAAAATCTAGAA[C/T]GTGTGTATACATAAA | 55120 |
| rs779780781 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233885 | AGATAGGTAGAGACA[C/T]CTTTTGGAAACTGGG | 55120 |
| rs779787603 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | FANCL | GRCh38.p7 | 2:58204082 | ATTCACAGAGTTCAT[C/T]TCACAAAGTATTTTC | 55120 |
| rs779809687 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227640 | GTTCCTCCACCGATA[C/T]ATTTCTCTCAACGTC | 55120 |
| rs779816440 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58178430 | GGCTGGTTCAACATA[A/C]GCAAATCAATAAACG | 55120 |
| rs779820927 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58238122 | CTGAATGCAGCCCAA[A/C]ACAAATTAATAAACT | 55120 |
| rs779834767 | snp | C/T | 0.000116435 | 0.00762914 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162856 | ATATCAAAACACTGA[C/T]AAAACTTACAGATTT | 55120 |
| rs779873811 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239042 | ATGAGAAAGCAGGCA[A/G]TGCTACTCCTTATAA | 55120 |
| rs779903784 | snp | A/T | 3.31279e-05 | 0.00406975 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159409 | TTGAATGAAGTAAAC[A/T]GTTTCCCACAAAAAA | 55120 |
| rs779907287 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228897 | TTTTTCCCATGCTAT[A/T]TCAATATGTCAACAG | 55120 |
| rs779974378 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169900 | CAAGAAATATCAGAC[C/T]ATGTGAAAAGACCAA | 55120 |
| rs780027977 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213978 | ACTCTAGGGAGCATC[A/G]TTCACACAGAATGCC | 55120 |
| rs780035489 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172349 | TAACTGGGAGGCACC[A/G]CCCAGTAGGGGCAGA | 55120 |
| rs780083917 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58201472 | AACAAATTTTAACCA[A/C]GTCTGTTCTGTGACT | 55120 |
| rs780118756 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58211214 | ATCTAGGCGGAGGTT[-/C]TGAAACCTCAGTTCT | 55120 |
| rs780133163 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58197583 | TAATCATACCACCTT[A/G]TATCTATGTTATAGT | 55120 |
| rs780185177 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58214771 | CCCCACCTCAGCCCC[A/C]CAAAGTACTGGGATT | 55120 |
| rs780185479 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58167474 | TATTCCTTTGTATAC[C/T]CAAGATAAGGTTAAC | 55120 |
| rs780219890 | in-del | -/ACTT | | | intron-variant | FANCL | GRCh38.p7 | 2:58185958 | GAAATATTGAGAAAC[-/ACTT]ACATTCTGCAAACTA | 55120 |
| rs780243941 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58223709 | TTCAGTGGCTCAGCT[A/C]TAAAATAGAAATAAA | 55120 |
| rs780268295 | in-del | -/GAT | 6.66722e-05 | 0.00577336 | utr-variant-3-prime, cds-indel, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159695 | TATTTTTTCTCTGAA[-/GAT]GATACCAAAATTCCT | 55120 |
| rs780276907 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58185598 | TTGGCAATGCTTGCC[A/G]ATTTTTATGCTGGAA | 55120 |
| rs780301612 | snp | C/T | 1.6722e-05 | 0.00289149 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159745 | TTTCCAGCTCTTCAC[C/T]GAAATGTTGTATTCT | 55120 |
| rs780310527 | snp | C/G | | | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162012 | AAATATACACAGCTA[C/G]GCTAAAAAAAGAGAT | 55120 |
| rs780321019 | snp | A/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161024 | AGTGGCATTGCCTGA[A/G]TGCTGTGAGACTCAG | 55120 |
| rs780325689 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58236830 | TTAATATTGGAAAAT[A/C]CAGATTTCAGAGAAA | 55120 |
| rs780346651 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242645 | TGACAACTTACCCCA[A/G]TTTATTACCATTAGA | 55120 |
| rs780348127 | snp | A/C/G | 0.000196913 | 0.00992093 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241357 | GCTCTAGACCTGCTG[A/C/G]GTCCTGCACATGCGC | 55120 |
| rs780404439 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58231000 | TTCTGCCACCACACA[A/G]AACTTACTTGCATCT | 55120 |
| rs780408979 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58181337 | TGTTTATAATATCTG[C/G]AATAGACATAACTAA | 55120 |
| rs780414432 | snp | A/G | 1.68128e-05 | 0.00289933 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163455 | CAGCTCCAAGAAAGA[A/G]GCACTCAGGAAGCAT | 55120 |
| rs780434756 | snp | A/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241637 | TTGAAAGACTGTTAC[A/T]ACTTTGGTGTTGCAT | 55120 |
| rs780447628 | snp | C/T | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163261 | TAACTATCATTATTG[C/T]GGTGAACCGAGATCG | 55120 |
| rs780511644 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212651 | ACTGTTTAATTCTTA[-/T]TTTTTTTAATAGGCC | 55120 |
| rs780529151 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200918 | ACTTCATATCTGAGT[G/T]AAATGAGTATTTGCA | 55120 |
| rs780598090 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172475 | GCAGCCACCGCTACT[A/G]GTACCCAGGCAAACA | 55120 |
| rs780598562 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170089 | CACATAATGGTCAGA[C/T]TCATCAAGGTTGAAA | 55120 |
| rs780614415 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242485 | CAAAACCTAAGATCA[C/T]TCTCTGACCTTCTCC | 55120 |
| rs780633246 | snp | A/G | 8.73889e-05 | 0.0066096 | intron-variant | FANCL | GRCh38.p7 | 2:58226695 | CAAGACTTGCAGTAT[A/G]GTAACAGTGTCAGAA | 55120 |
| rs780648809 | in-del | -/AC | 1.74436e-05 | 0.00295322 | intron-variant | FANCL | GRCh38.p7 | 2:58226699 | ACTTGCAGTATGGTA[-/AC]AGTGTCAGAAAAAAA | 55120 |
| rs780648962 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58171937 | CGGGTTTAAAAAACG[A/G]CACACCAGGAGATTA | 55120 |
| rs780652198 | snp | G/T | 1.8563e-05 | 0.0030465 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163535 | AGAATGAAACAAGAT[G/T]AAATCTTTTAGAAGT | 55120 |
| rs780722369 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168460 | CAACCCGCAGATCAG[C/G]AGATTCCCTCTGGTG | 55120 |
| rs780735755 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170637 | CATCTCACGTGCAAA[C/G]AAACACACAGGCTCG | 55120 |
| rs780745258 | snp | C/T | 8.27616e-05 | 0.00643226 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159654 | CATCATCATACCTGT[C/T]CTTTTGATGTTAGTA | 55120 |
| rs780790604 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58213598 | TCATCCTAGGCCAGG[A/C]ATGGCAGCGAACACC | 55120 |
| rs780794056 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58214934 | TATCACATCCTTAAC[A/G]CTTCAACTGATTTTT | 55120 |
| rs780855374 | in-del | -/CCTGAACTCTAAGTACATTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58222425 | ACCTCTAAAGAAAGG[-/CCTGAACTCTAAGTACATTA]CCTAAACTGACATAT | 55120 |
| rs780871027 | snp | C/T | 1.73836e-05 | 0.00294813 | intron-variant | FANCL | GRCh38.p7 | 2:58226809 | AATATTTCCAATTAA[C/T]TTCATTTGCACAATA | 55120 |
| rs780902102 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222249 | GGTCATGCAAAATGT[C/G]AATTTTTATGCCATG | 55120 |
| rs780911747 | in-del | -/A | 0.000136977 | 0.00827464 | intron-variant | FANCL | GRCh38.p7 | 2:58194203 | CAAGAATACTTCACC[-/A]AGCCTGCACTTAGTG | 55120 |
| rs780914086 | snp | C/T | 1.73582e-05 | 0.00294598 | intron-variant | FANCL | GRCh38.p7 | 2:58232159 | TTTTTATCTTTCACT[C/T]AATGCTGAGAAGTTA | 55120 |
| rs780981205 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58202243 | ACCTTTTTCCTAAAA[-/A]AAAAAAAAAAAAAAA | 55120 |
| rs781022842 | in-del | -/AT | 1.65203e-05 | 0.002874 | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159485 | ATTTTACCAGTCCAG[-/AT]ATATTCAAGAAGTCA | 55120 |
| rs781060245 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58229297 | TTTTTTTCTAATCTT[C/T]AAAGGAATTTTCAGG | 55120 |
| rs781071191 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58211334 | ACTGGCCCTTTTCAG[A/C]CACAGCTGGAGCAGC | 55120 |
| rs781078040 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58234127 | TCATCAATGCAAAGC[C/T]ACTATGAGACAAAGA | 55120 |
| rs781090269 | snp | C/T | 1.76114e-05 | 0.00296739 | intron-variant | FANCL | GRCh38.p7 | 2:58198710 | GCTTCTGTGTGTTAA[C/T]ATCACTGAGGTATTT | 55120 |
| rs781142304 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58187281 | GGACACGGATGAAGC[C/T]GGAAACTATCATTCT | 55120 |
| rs781257747 | snp | A/T | | | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159789 | CCTTCCAGACATTTT[A/T]AAGGTAATTGGCTTT | 55120 |
| rs781295433 | snp | A/G | 1.65181e-05 | 0.00287381 | synonymous-codon, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221974 | TCCTATCTCTTCAAT[A/G]AGGCTTGAGTAGAAC | 55120 |
| rs781350185 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58232267 | TTAAAATATATGCAA[A/C]ACAATATTGCATTTG | 55120 |
| rs781357185 | snp | A/C | 1.66103e-05 | 0.00288182 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232073 | CATTCTTCAGTTGTA[A/C]ATCTTCAGGCAACAC | 55120 |
| rs781375167 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58186651 | GAATTGCCCTAAAGG[A/G]GATTCAGTCTCTCAC | 55120 |
| rs781384016 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212575 | TCAAAGCAAAAGTAT[C/T]TGGTACTTTCAACTC | 55120 |
| rs781409397 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172564 | ACAGAGGGTCTGTTT[A/G]TTAACAGAAAGGACT | 55120 |
| rs781429494 | snp | G/T | 1.66018e-05 | 0.00288108 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161516 | GACAATATTTTTATT[G/T]TTTACCTCATATAAG | 55120 |
| rs781438290 | snp | C/G | 1.68724e-05 | 0.00290446 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163442 | GTCATACCATGGTCA[C/G]CTCCAAGAAAGAAGC | 55120 |
| rs781444538 | in-del | -/CTGACTC | | | intron-variant | FANCL | GRCh38.p7 | 2:58194975 | TAAAGTCCAGAAACA[-/CTGACTC]CAAAGAGAAAATACA | 55120 |
| rs781449262 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58218409 | TGCAAAACTGATTAA[A/G]AAAAATTAAAAAGGC | 55120 |
| rs781474494 | snp | A/C/G | 3.58104e-05 | 0.00423133 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241327 | ATGGCTCGAAGTCCG[A/C/G]AGAAACACAGAAAAG | 55120 |
| rs781524477 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58199215 | CGGTGTTGAGTAAAA[C/G]GTAATGAATTAAGTC | 55120 |
| rs781525588 | snp | A/G | 1.65581e-05 | 0.00287728 | intron-variant | FANCL | GRCh38.p7 | 2:58204278 | GGGAGAGCTGGAGAG[A/G]GGAACTGGAGATGGT | 55120 |
| rs781529898 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242688 | CAACCGTACTTCCCC[A/G]CAACTGTCCACTGTT | 55120 |
| rs781533301 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58182055 | TTTGAAATGTCTATG[A/C]TAAGCATTCTGAATC | 55120 |
| rs781533833 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58218795 | GTATGAGATTTCAGA[C/T]ATACCAAGCAAGTGG | 55120 |
| rs781539073 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58239919 | AAATATTTTTAGACA[C/T]GTAAAATGTTTAAGA | 55120 |
| rs781539412 | snp | A/G | 0.00027371 | 0.0116953 | intron-variant | FANCL | GRCh38.p7 | 2:58194219 | AGCCTGCACTTAGTG[A/G]CACACTTACAGGCAA | 55120 |
| rs781556579 | snp | A/C/T | 6.61184e-05 | 0.00574941 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159637 | GATGTTTATTATTAT[A/C/T]GCATCATCATACCTG | 55120 |
| rs781559042 | snp | C/T | 1.70603e-05 | 0.0029206 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241308 | GCTCGCTTCCGTCAC[C/T]GCCATGGCTCGAAGT | 55120 |
| rs781567227 | in-del | -/CT | | | intron-variant | FANCL | GRCh38.p7 | 2:58178548 | CCTTCATGCTAAAAA[-/CT]CTCAATAAATTAGGT | 55120 |
| rs781588636 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58207681 | CAGAAAAAAATATCT[C/T]GGTGTTTGGTGTATG | 55120 |
| rs781611808 | snp | A/C | 1.67156e-05 | 0.00289093 | utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159739 | TTTAAGTTTCCAGCT[A/C]TTCACCGAAATGTTG | 55120 |
| rs781651814 | snp | G/T | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164213 | TCTATTTTTTGAAGG[G/T]ACATAGTGTAACTGC | 55120 |
| rs781666144 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58239111 | AGAAAATCATCATTT[A/G]GCAACCGTGATAGTA | 55120 |
| rs781738464 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58178122 | TAACCAAAAAAAGCC[C/G]AGAACCACACAGATT | 55120 |
| rs796136269 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217168 | ATATTTATATATTTT[A/T]TATATATATATATAT | 55120 |
| rs796214496 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58215705 | CTGCTATTAAGTGGC[-/A]AAAAAAAAAAAAAGC | 55120 |
| rs796277560 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217177 | TATTTTATATATATA[G/T]ATATATATATATATA | 55120 |
| rs796374656 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58238109 | GCCCAGGACAGCTCT[C/G]AATGCAGCCCAACAC | 55120 |
| rs796403448 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58205189 | TATCACTATATGCCA[C/T]TTAGATACTGACCAG | 55120 |
| rs796409160 | snp | A/G | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242928 | TGGCAATAGGGCTCA[A/G]CAGTCTGCGTTTTAA | 55120 |
| rs796528462 | in-del | -/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242513 | CCCATCCTTCTTCCC[-/T]TGAGGCGGGTCATTG | 55120 |
| rs796557555 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58226076 | TACATACAATATCCA[A/G]AATTTCCTTTAAAAT | 55120 |
| rs796646796 | in-del | -/ATTTATATATATATTTATATATTTTAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58217143 | TATTTTTATATATAG[-/ATTTATATATATATTTATATATTTTAT]ATATATATATATATA | 55120 |
| rs796713283 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58223140 | ATCTGCTTTATGATG[-/A]AAAAAAAAAAAACAA | 55120 |
| rs796725052 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58171652 | GAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 55120 |
| rs796769539 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58201738 | GGTTTACTTCTACTT[A/T]TTTATTATTTACATA | 55120 |
| rs796838368 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58198067 | GTGTGTGTATTTATG[-/C]CATGGGTGTGGGTGT | 55120 |
| rs796874236 | in-del | -/TA | | | intron-variant | FANCL | GRCh38.p7 | 2:58198415 | AGAGATAACTTAAAG[-/TA]TACAGAAGAGTGTGC | 55120 |
| rs796912489 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58181710 | TTTAGATGGTGGATA[A/C]ATGGGTATTCACCAT | 55120 |
| rs796987370 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217165 | TATATATTTATATAT[A/T]TTATATATATATATA | 55120 |
| rs864622189 | snp | G/T | | | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163516 | TTGTTTCATTCTAGG[G/T]AATAATGTTTCCATA | 55120 |