| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs274899 | snp | C/T | 0.475235 | 0.108485 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643234 | TCTTCAACAGGACTG[C/T]GTGCAACGCCAAGGC | 146845 |
| rs364423 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626786 | CTTTCTAACTAAGTA[C/G]TCCATCATTATAACT | 146845 |
| rs368787 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622927 | GATCTCCaaagtaca[C/T]attgaaatattctat | 146845 |
| rs389995 | snp | C/T | 0.495818 | 0.0455352 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636253 | TAGTTATTTTTCTTT[C/T]TCTTTCTTTCTTTCT | 146845 |
| rs418706 | snp | A/C | 0.291235 | 0.246576 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635332 | AAAAGATTCCAAGAG[A/C]TTTTTCCCCTTTGCT | 146845 |
| rs419461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639227 | ctgaggtcaggagtt[C/T]gagaccagcctagcc | 146845 |
| rs755307 | snp | A/G | 0.484491 | 0.0866827 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591073 | TCCAGCCTGGGAAAC[A/G]AGAGTGAAACTCCAT | 146845 |
| rs922016 | snp | A/G | 0.36955 | 0.219562 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600621 | ccaggctggcgtgca[A/G]tggcgagatgtcggt | 146845 |
| rs1698285 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629748 | cgtgtgtcatcacga[G/T]gggctaattttttgt | 146845 |
| rs1807022 | snp | A/C/G | 0.539677 | 0.182521 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589481 | CTCACGCCTGAAATC[A/C/G]CAGCACTTTGGGAGG | 146845 |
| rs1968765 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585442 | gggaggctaaggtgg[A/G]cggatcacgaggtca | 146845 |
| rs1979287 | snp | A/G | 0.127944 | 0.218179 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595493 | ACGGGCTGTGGCGAC[A/G]CTCTTCAACTTTTTT | 146845 |
| rs1979288 | snp | A/T | 0.0763149 | 0.179815 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595603 | ATTGGTCCATTCTGA[A/T]GTCCATGAGCAACAT | 146845 |
| rs2016355 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600327 | gctcactgcaacttc[C/T]gcctcccaggttcaa | 146845 |
| rs2034948 | snp | C/T | 0.477004 | 0.104734 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609885 | ATACATGCTCAAGTT[C/T]GAAAGCCACAGCCCC | 146845 |
| rs2054229 | snp | C/T | 0.35809 | 0.225425 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603092 | TTTTTTGTTTTGTTT[C/T]GTTTTGTTTTCCTAG | 146845 |
| rs2085579 | snp | A/G | 0.393619 | 0.204631 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597650 | tctactaaaaataca[A/G]aaattagctgggcgt | 146845 |
| rs2134311 | snp | C/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626926 | TCATGAAAAAATGTA[C/G]ACATTGCTTGAGATG | 146845 |
| rs2271003 | snp | A/G | 0.00674831 | 0.0576942 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643217 | TGATGAGATGTCTCT[A/G]AGCCTTGGCGTTGCA | 146845 |
| rs2315137 | snp | A/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589745 | ctcaaaaaaaaaaaa[A/T]aaaaaaaaagaaaag | 146845 |
| rs2315138 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589749 | aaaaaaaaaaaaaaa[A/T]aaaaagaaaagaaAT | 146845 |
| rs2654718 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626214 | TTCCAAACTCTCTAC[A/G]CTTGATGGCCTATCC | 146845 |
| rs2654722 | snp | C/T | 0.404559 | 0.196498 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635999 | CCAACATGGTGAAAC[C/T]CCTTCTCTACTAAAA | 146845 |
| rs2872833 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579195 | TTAGAGCTAGTATAG[C/T]TTTTTAAAATAAACA | 146845 |
| rs2937972 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627249 | gcacagtggctcaca[C/T]ctgtaatcccagcac | 146845 |
| rs2937973 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629872 | TGGGATTACAGGAGT[A/G]AGCCACTGCACCCGG | 146845 |
| rs3060109 | in-del | -/TTTT/TTTTTTT/TTTTTTTTT | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589815 | CTTTTTTTTTTTTTT[-/TTTT/TTTTTTT/TTTTTTTTT]GCAAGCAGAAAAAGC | 146845 |
| rs3968764 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627442 | acttggctttactcc[A/G]cctcccgggttcacg | 146845 |
| rs4062872 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627436 | ctttactccgcctcc[C/T]gggttcacgccattc | 146845 |
| rs4062873 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9627434 | ttactccgcctcccg[G/T]gttcacgccattctc | 146845 |
| rs4275899 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579254 | AACTTTCATAAGGCT[C/T]GGGAGAGAAGATTTT | 146845 |
| rs4341784 | snp | G/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625662 | GGCTCCCACATGTGA[G/T]AAAGCCACATGCTAA | 146845 |
| rs4791352 | snp | C/T | 0.349671 | 0.229272 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601228 | GAGAACACATGGACC[C/T]GGGAAAGGGAACATC | 146845 |
| rs4791353 | snp | A/G | 0.398894 | 0.200825 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601625 | CATTATAAGTCGTGA[A/G]CAAGACCTAGAAATA | 146845 |
| rs4791854 | snp | A/C | 0.372391 | 0.217992 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583182 | CCTGCAATTAGAAAA[A/C]TATAAAAAATTTTTA | 146845 |
| rs6503230 | snp | C/T | 0.394538 | 0.203982 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576047 | CTCAGTTAAAATTGT[C/T]AAATAGAAACAAAGC | 146845 |
| rs6503231 | snp | A/C | 0.434976 | 0.168179 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576359 | TGTACGCCTGATTAC[A/C]TATTTTTTAAATGCC | 146845 |
| rs6503232 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586427 | AATTAGCAGGGCGTG[C/G]TGGTGCATGCCTGTA | 146845 |
| rs6503233 | snp | G/T | 0.0788843 | 0.182262 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598078 | ACCTGCCTCGTGGTG[G/T]TGTTATGAGGATCGA | 146845 |
| rs6503234 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608512 | CCATGATGAAAGGAA[C/T]GGGATGTTATAAACT | 146845 |
| rs6503235 | snp | A/G | 0.411273 | 0.191026 | missense | CFAP52 | GRCh38.p7 | 17:9612460 | CACTTTGATGCTGTC[A/G]AGGATATTGTCTTTC | 146845 |
| rs6503236 | snp | A/G | 0.217551 | 0.247885 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614606 | ATTCATTTGTTTATT[A/G]AACAAATTCATTTAT | 146845 |
| rs7207303 | snp | C/T | 0.22263 | 0.248497 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585390 | TTTTAAAGTGTTggc[C/T]gggcgcggtggctca | 146845 |
| rs7209502 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611995 | TAAAGGGGTTAGTTG[A/C]TGTGGTCATTTGTAC | 146845 |
| rs7210038 | snp | C/T | 0.373598 | 0.21731 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575731 | AGTGATTGCCTGCTC[C/T]CCGGAAGCCCGGCCT | 146845 |
| rs7214348 | snp | A/G | 0.49645 | 0.0419827 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591663 | cggaaaggatcactt[A/G]agcctagaagttcaa | 146845 |
| rs7217559 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596059 | GATATATATGTGTGT[A/G]TATATATATATATAT | 146845 |
| rs7220517 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597996 | GAGTGAGACGGAGCC[A/G]GGTGTGAATCCCTGC | 146845 |
| rs7220694 | snp | A/G | 0.0364509 | 0.129988 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643868 | GGAGTTGGCCATTAC[A/G]TCTTTCTTCTGTGCT | 146845 |
| rs7222390 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593486 | ttcgagacgcagtct[C/T]gctctcttgcccagg | 146845 |
| rs7222448 | snp | G/T | 0.383379 | 0.211448 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596722 | TGTGTGTGTGTGTGt[G/T]ttttttttttgagat | 146845 |
| rs7224675 | snp | C/T | 0.397271 | 0.202018 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583582 | ACTTATGAAGAAACA[C/T]ATCCTGTTTTTAAAA | 146845 |
| rs7224680 | snp | C/T | 0.15665 | 0.231917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635894 | TAACGAATGCAAggt[C/T]gggcgtggtggcttc | 146845 |
| rs7224817 | snp | A/C | 0.411526 | 0.190812 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575781 | CACCGCCGCCCTCAC[A/C]CGGGACTCACCAGGG | 146845 |
| rs7225814 | snp | A/G | 0.228842 | 0.249103 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608445 | ACTATTACCCAGAGG[A/G]ACACTGCCCATTTAA | 146845 |
| rs7350938 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9618745 | caacctgctcctgaa[C/T]gactactgggtacat | 146845 |
| rs7359617 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619303 | aagactaaaccagga[A/G]gaagttgaatctctg | 146845 |
| rs7359621 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619384 | aaccaaaaagagtcc[A/G]ggaccagatggattc | 146845 |
| rs7503761 | snp | A/G | 0.353803 | 0.227431 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580880 | tacaattcttaatga[A/G]gataatctttgaGCT | 146845 |
| rs7503872 | snp | A/G/T | 0.0115144 | 0.0749975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589751 | AAAAAAAAAAAAAAA[A/G/T]AAAGAAAAGAAATGT | 146845 |
| rs8064915 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578389 | acattactgaaatca[C/G]tctgttgtccaatca | 146845 |
| rs8067557 | snp | G/T | 0.379942 | 0.213577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615752 | gtagctgggatgcag[G/T]catgtaccaccatgc | 146845 |
| rs8068403 | snp | C/T | 0.151001 | 0.229563 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615546 | TGTTTTATTTGGTTC[C/T]GTTTTAACCTTTGCT | 146845 |
| rs8076248 | snp | C/T | 0.372391 | 0.217992 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582845 | tttcgccatattggc[C/T]aggctggtctcaaac | 146845 |
| rs8080111 | snp | A/G | 0.389903 | 0.207189 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598693 | TTGAACCTGGGAGGC[A/G]GAAGTTGCGGTGAGC | 146845 |
| rs8080667 | snp | C/T | 0.221439 | 0.248363 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597757 | gcagtgagcagagat[C/T]gcgccactgcactcc | 146845 |
| rs8182308 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9618839 | cagaatctctgggac[A/G]cattcaaagcagtgt | 146845 |
| rs9674652 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9619132 | gaaaaaaagagagaa[A/G]aatcaaatagacaca | 146845 |
| rs9786533 | snp | A/C | 0.48 | 0.0979796 | intron-variant | CFAP52 | GRCh38.p7 | 17:9618754 | CATTTCGTTATGTAC[A/C]CAGTAGTCGTTCAGG | 146845 |
| rs9807067 | snp | A/C | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637552 | CTTGGTACAGTATCT[A/C]AGGCAGGGGTTCTAT | 146845 |
| rs9889489 | snp | C/T | 0.468349 | 0.121752 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603741 | agatgatgtagatga[C/T]gggttgatgggtgca | 146845 |
| rs9889814 | snp | C/T | 0.431029 | 0.17242 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603328 | ATTCTCCTGACTCAG[C/T]CTCCAGAGTAGCTGG | 146845 |
| rs9889912 | snp | A/G | 0.0941369 | 0.195465 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575734 | GATTGCCTGCTCTCC[A/G]GAAGCCCGGCCTCCC | 146845 |
| rs9891338 | snp | C/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605692 | agagtgagactccat[C/T]tgaaaaaaaaaaaaa | 146845 |
| rs9891626 | snp | C/T | 0.0193679 | 0.0964822 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575747 | CCGGAAGCCCGGCCT[C/T]CCCGAAGGTCCCTCC | 146845 |
| rs9897098 | snp | A/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580129 | AGATcaggagtctac[A/T]aactatagcccatgg | 146845 |
| rs9897757 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634440 | acctgagctcaggag[A/T]ttgagaccagcctgg | 146845 |
| rs9898166 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589017 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 146845 |
| rs9900804 | snp | A/T | 0.486595 | 0.0807641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622575 | agaagaagaagaaGA[A/T]GATGATGATGATGAG | 146845 |
| rs9901292 | snp | A/G | 0.112631 | 0.208878 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602371 | tgaatgagaacatgc[A/G]gtgtttggttttctg | 146845 |
| rs9902732 | snp | A/G | 0.148326 | 0.228391 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601903 | TAGATACTTTTCCAC[A/G]TAGCAGATATTCTCA | 146845 |
| rs9904304 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589727 | acaagagcgagactc[C/T]gtctcaaaaaaaaaa | 146845 |
| rs9907091 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592795 | ATTTCCACTTCTAAA[C/T]TATTATTAATAATGG | 146845 |
| rs9907855 | snp | A/G | 0.112983 | 0.209108 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602830 | acgtgagatggtatc[A/G]cattgcagttttgat | 146845 |
| rs9909865 | snp | C/T | 0.125874 | 0.217008 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602393 | ggttttctgttcctg[C/T]tttagtttgctgaga | 146845 |
| rs9911158 | snp | C/T | 0.468949 | 0.12067 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603509 | ccaccacacccggcc[C/T]TAAGTagatatttca | 146845 |
| rs9911407 | snp | A/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596061 | TATATATGTGTGTGT[A/G]TATATATATATATAT | 146845 |
| rs9911693 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591258 | ggtcaggctggtctc[A/G]aactcccaacctcag | 146845 |
| rs9913344 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591210 | GCCTGGCTAATTTTG[C/T]ATTTTTAGTAGAGAC | 146845 |
| rs9913960 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591163 | ctgcctcagcctccc[A/G]aacagctgggattac | 146845 |
| rs9914158 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591183 | GCTGGGATTACAGGC[A/G]TGCACCACCATGCCT | 146845 |
| rs9916826 | snp | C/G | 0.482683 | 0.0914256 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588597 | cttcagcatgggctg[C/G]acctggaccctggga | 146845 |
| rs10548437 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597804 | GGGACTCTGTCAGAA[-/AG]AGAGAGAGAGAGAGA | 146845 |
| rs10656812 | in-del | -/A/AAAAAAAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636194 | AAAGAAAGAAAGAAA[-/A/AAAAAAAAA]GAAAGAAAGAAAGAA | 146845 |
| rs10688020 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597830 | AGAGAGAGAGAGAGA[-/G]AAGAGAGAAAGAGAG | 146845 |
| rs10699113 | in-del | -/TGTGTG/TGTGTGTG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596051 | GTATGTAGATATATA[-/TGTGTG/TGTGTGTG]TGTGTGTGTATATAT | 146845 |
| rs11078808 | snp | A/G | 0.473451 | 0.112115 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607215 | ACCAGGCATGATGGC[A/G]CATGCCTATAATCCC | 146845 |
| rs11078809 | snp | A/G | 0.187053 | 0.241946 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607282 | ACTTGGGAGGCAGAG[A/G]GTGCAGTGAGTTGAG | 146845 |
| rs11281941 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636191 | AAAAAAGAAAGAAAG[-/A]AAAGAAAGAAAGAAA | 146845 |
| rs11296135 | in-del | -/A | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586585 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAAGAAA | 146845 |
| rs11309835 | in-del | -/C | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585618 | GAAGGTTGCAGTGAG[-/C]CCAAGACTGCACCAT | 146845 |
| rs11347755 | in-del | -/T | 0.211819 | 0.247067 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614158 | TCTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 146845 |
| rs11378454 | in-del | -/T/TT/TTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594893 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GACAGTGTTTTGCTG | 146845 |
| rs11386649 | in-del | -/A/AA | 0.499218 | 0.0197529 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580318 | AAAAAAAAAAAAAAA[-/A/AA]GCCAGACCCTGTAAA | 146845 |
| rs11651115 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589024 | ggagaatcacttgaa[C/G]ctgggaggcagaggt | 146845 |
| rs11651385 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614578 | GTAATAAATGAATTC[A/G]tttattataaaaatt | 146845 |
| rs11652942 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616061 | gacgcagaagacggg[G/T]gatttctgcatttcc | 146845 |
| rs11653066 | snp | C/T | 0.37138 | 0.218556 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608452 | CCCAGAGGGACACTG[C/T]CCATTTAATAAATAC | 146845 |
| rs11653477 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603500 | aggcgtgagccacca[C/T]acccggccCTAAGTa | 146845 |
| rs11653956 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629516 | ttttctttctttctt[C/T]cttctttcttttttc | 146845 |
| rs11654017 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623687 | ttgtttgtttgtttg[C/T]ttgtttgtttgttta | 146845 |
| rs11654310 | snp | C/T | 0.24932 | 0.249999 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587133 | TATTTGGTTTTCTAC[C/T]CCTGCATTAGGTTGC | 146845 |
| rs11655590 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610171 | ACATCCAAGTATTGT[C/T]GATAATACAAGATGC | 146845 |
| rs11656135 | snp | G/T | 0.388775 | 0.207946 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606102 | taaaaacaaaaaTAg[G/T]ccaggcaaggtggat | 146845 |
| rs11656195 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615917 | agcacaggcctctca[A/C/G]attataggcatgagc | 146845 |
| rs11656236 | snp | A/G | 0.277778 | 0.248452 | intron-variant | CFAP52 | GRCh38.p7 | 17:9616052 | agcgtgagcgacgca[A/G]aagacgggtgatttc | 146845 |
| rs11656351 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586258 | TGTAGAACCTGATCC[A/G]ATTTCTAGAAAAGTG | 146845 |
| rs11656370 | snp | C/T | 0.35445 | 0.227135 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600693 | cctcagcctcccaag[C/T]agctgggactacagg | 146845 |
| rs11656430 | snp | A/G/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586456 | taatcccagctactc[A/G/T]ggaggctgagacagg | 146845 |
| rs11656540 | snp | A/G | 0.434976 | 0.168179 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577239 | AAAGGGCTGGGAGGG[A/G]ACGTGTGTTTGAGCA | 146845 |
| rs11656567 | snp | A/G | 0.137867 | 0.223442 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640983 | AGTCTATCATTGATG[A/G]GCATTTAGGTTGATT | 146845 |
| rs11657542 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629517 | tttctttctttcttt[C/T]ttctttcttttttct | 146845 |
| rs11657544 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629524 | ctttctttcttcttt[C/T]ttttttcttccttgc | 146845 |
| rs11657546 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629534 | tctttcttttttctt[C/G]cttgcttgcttGCtt | 146845 |
| rs11657876 | snp | A/C | 0.487495 | 0.0780784 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587024 | CTCTCCCTCTCCCAC[A/C]CTCCACCCTCAACAG | 146845 |
| rs11657922 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587162 | GCTAAGGATAATGGC[C/T]TCCAGCTCCATCCAT | 146845 |
| rs11868054 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583987 | CAAAGACCACCTCAC[C/T]GAGTTGAGTCTCTGA | 146845 |
| rs11869132 | snp | A/T | 0.039522 | 0.134904 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581417 | TAGATGTATATAAAC[A/T]AATGAGGAAAGATGT | 146845 |
| rs11869154 | snp | A/T | 0.039522 | 0.134904 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581731 | CCCAAGATAGGTAGG[A/T]GCTGGTTCTATTGCT | 146845 |
| rs11869172 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581809 | GCAGCCAATTGAGAG[A/G]TGTAACATAATTGGC | 146845 |
| rs11870706 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607257 | tgggtgagtcacaag[A/G]atcgcttgaacttgg | 146845 |
| rs11870731 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577268 | CAACCCCCTGAGGGG[A/T]TGTTGTTGGTCCTCT | 146845 |
| rs11870993 | snp | C/T | 0.039522 | 0.134904 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581416 | ATAGATGTATATAAA[C/T]TAATGAGGAAAGATG | 146845 |
| rs11871087 | snp | C/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606772 | AAAAAATTCACTCCA[C/T]GTTTTGTCTCCTCAT | 146845 |
| rs12051722 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596901 | tttatatttttaata[A/G]agacggggttttcac | 146845 |
| rs12051784 | snp | A/G | 0.482083 | 0.0929373 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598625 | AAGTAGCCAGGTGTG[A/G]TGGTAGGTGCCTGTA | 146845 |
| rs12051818 | snp | A/G | 0.016031 | 0.0880824 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598771 | GTTTCAAAAAAAAAA[A/G]AAGAAAAAGTTCACC | 146845 |
| rs12103586 | snp | A/G | 0.208779 | 0.246578 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610940 | GGGCTAGCAACAGAT[A/G]TAAAGGAGCAACATC | 146845 |
| rs12451615 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9594994 | ctcccgggttcaagc[A/G]attctcctgcctcag | 146845 |
| rs12453336 | snp | A/G | 0.435119 | 0.16802 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578430 | tatggcgggttgaac[A/G]gggcttcagttagta | 146845 |
| rs12453912 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578595 | tggagtctcgctctg[G/T]tgtgtaatggcacaa | 146845 |
| rs12453913 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578596 | ggagtctcgctctgt[A/T]gtgtaatggcacaat | 146845 |
| rs12600506 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636006 | ggtgaaaccccttct[C/G]tactaaaaataaaaa | 146845 |
| rs12601194 | snp | C/T | 0.00332778 | 0.0406548 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580062 | CCCATGATTTTCCTA[C/T]TATGGTATACAAAGA | 146845 |
| rs12601904 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608830 | TATTAATAAAATAAA[A/G]AAAAATAAGCTATGG | 146845 |
| rs12602008 | snp | C/T | 0.349233 | 0.229462 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608784 | TGTGCTTATTCAGCA[C/T]CTCCTCCAACCAAAC | 146845 |
| rs12602375 | snp | A/C | 0.278664 | 0.248351 | intron-variant | CFAP52 | GRCh38.p7 | 17:9621964 | ACATATGTAACTAAC[A/C]TGCACAATGTGCACA | 146845 |
| rs12602714 | snp | C/T | 0.484632 | 0.086302 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588535 | catcttccacctgcc[C/T]acagcccccgagtgt | 146845 |
| rs12944432 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9632705 | ggcttaggcaactgg[A/C]tgggtggtggcaacc | 146845 |
| rs12948579 | snp | A/G | 0.00475057 | 0.0485048 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615901 | tacctcggcctccca[A/G]agcacaggcctctca | 146845 |
| rs12951385 | snp | C/T | 0.45692 | 0.1403 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585543 | AGGTGTGGTGGCGGG[C/T]GCCTGTAATCCCAGC | 146845 |
| rs16958487 | snp | C/T | 0.0944967 | 0.195752 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576560 | CATTTCCAAGAATGC[C/T]AATGAACTCGAACTC | 146845 |
| rs16958489 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584002 | CGAGTTGAGTCTCTG[A/G]ATCAGGGAAATTAGA | 146845 |
| rs16958496 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589441 | GACTGTTTCTGATAA[A/T]AAATGTATTGGCCGG | 146845 |
| rs17852264 | snp | A/T | | | missense | CFAP52 | GRCh38.p7 | 17:9598292 | ATCTGGCCAACTGAG[A/T]GCCAAACAGGACAGT | 146845 |
| rs28432152 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582833 | GTAGAGACAGGGTTT[C/T]GCCATATTGGCTAGG | 146845 |
| rs28555611 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584835 | ACCATGTTGGCCAGG[C/T]TGGTCTTGAACTCCT | 146845 |
| rs28577148 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615057 | AAGGGTAACTTTCTA[A/C]AAGGAGATTTAAGAA | 146845 |
| rs28599811 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606339 | AGTGAGCTGTGATTG[C/T]GCCACTGCACTCCAG | 146845 |
| rs28720726 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639773 | AGGAGCAGCATCTGA[A/G]TGAGGCCTGAATGAC | 146845 |
| rs28814717 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605220 | GTAAGTAAAGGGATA[C/T]GTAAACTGTGATACA | 146845 |
| rs28877412 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604530 | CCCAGCACTTTGGGA[A/G]GCTGAGGCGGGCCGA | 146845 |
| rs33978485 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589753 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAATGTATC | 146845 |
| rs34162768 | snp | C/T | 0.11963 | 0.213316 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591544 | TCTATTTGGCCAGAT[C/T]TCTATGTTGTTGCCC | 146845 |
| rs34227157 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580034 | CATTCATCCATTGAC[-/C]TGGAGTAGGTAGCCC | 146845 |
| rs34259709 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611964 | TTTTAGGATTATTTT[-/T]CAGAAGTGGAATTAA | 146845 |
| rs34266215 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9599231 | TGAGCATTTCCTTGG[A/G]GTGTCACATCAGCAC | 146845 |
| rs34343098 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600000 | CCGCCTCGGCCTCCC[-/C]AAAGTGCTGATATTA | 146845 |
| rs34343666 | snp | A/G | 0.046775 | 0.145601 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585465 | CGAGGTCAGCAGTTC[A/G]AGACCAGCCTGACCA | 146845 |
| rs34406554 | in-del | -/G | | | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576848 | AGTGAGACACCGGGG[-/G]ACACCTGAAAGGCAG | 146845 |
| rs34434266 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589953 | TCTTCTCCTTCTTGG[-/G]CCCGGAGGTGCTCTT | 146845 |
| rs34510293 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612067 | TGCATTGCACAACCC[-/C]ATGTCAAAACGTTAT | 146845 |
| rs34511627 | in-del | -/T/TT | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588789 | TTTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTTTCAC | 146845 |
| rs34566219 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581222 | TCGGGAGGCTGAGGC[-/C]AGGAGAATGGCGTGA | 146845 |
| rs34567855 | in-del | -/AC | 0.0209421 | 0.100162 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606385 | CCCTGTCTCCAAAAT[-/AC]ACACACACACACACA | 146845 |
| rs34569016 | in-del | -/T | 0.402293 | 0.198259 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613903 | CGTTATTTCTAACAG[-/T]TGAAAATGGCTGCTG | 146845 |
| rs34653219 | snp | C/T | 6.59228e-05 | 0.00574083 | missense | CFAP52 | GRCh38.p7 | 17:9594294 | ATAAACATCTCATCC[C/T]GGCACCTGGAGAAGA | 146845 |
| rs34654539 | snp | A/C | 0.133435 | 0.221162 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622112 | TATTTTTATTTTCAC[A/C]TTTCCTCCACCATGT | 146845 |
| rs34662285 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583768 | TCTGACCATAGGTGA[A/G]CAATAATGGAGGACC | 146845 |
| rs34854955 | in-del | -/T | 0.479824 | 0.098392 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611246 | CATTCATGTATATAC[-/T]TTTTTTTTTTAAGTT | 146845 |
| rs34888799 | in-del | -/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591054 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC | 146845 |
| rs34908206 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9601576 | ATTTTTGTCTACTTT[-/G]ACTAACTAGATCTTA | 146845 |
| rs35013399 | in-del | -/A | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580703 | CAAAAAAAAAAAAAA[-/A]TGCTGTTAAAGCAGT | 146845 |
| rs35047038 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581419 | ATGTATATAAACTAA[-/A]TGAGGAAAGATGTCA | 146845 |
| rs35065797 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622252 | ACAATCTATATACAG[-/C]AAAATATGGTCTCAG | 146845 |
| rs35141945 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605225 | AAAGGGATACGTAAA[-/A]CTGTGATACATCCAA | 146845 |
| rs35203100 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602319 | TGATGTTCCCCTCCC[-/C]TGTGTCCATGTGTCC | 146845 |
| rs35212426 | in-del | -/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576180 | GTGAGACTTGCACGC[-/G]TGCGTAAACTCACTA | 146845 |
| rs35227739 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615824 | TTTTTTTTTTTCCCA[A/G]AAACAGGGTCTCACT | 146845 |
| rs35242661 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639845 | CTGGCAGAGGACACT[-/T]CCAGTAAGATGGAGC | 146845 |
| rs35309856 | snp | A/G | 0.298905 | 0.24517 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577797 | AACCACACACATAGA[A/G]CTCTGCAACTGAGGC | 146845 |
| rs35381857 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610279 | CTAATTTTTTACCCC[-/C]TTTGTTTTTAGTGTG | 146845 |
| rs35397077 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593826 | AAGAATTACCCGGAC[A/G]TGGTGGTGTGCGTCT | 146845 |
| rs35456032 | in-del | -/G | 0.0554779 | 0.157039 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591226 | ATTTTTAGTAGAGAC[-/G]GGGGTCTCTTCATGT | 146845 |
| rs35522999 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9612918 | AATAAATTACATGAG[-/T]ATATTCGACACTTTA | 146845 |
| rs35545462 | in-del | -/A/AA | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580758 | CAAAGGCAAAAAAAG[-/A/AA]AAAAAAAAAGGGTAA | 146845 |
| rs35581427 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9602893 | TTTTCTCATATGTTT[-/T]GTTGGCCGCATAAAT | 146845 |
| rs35645984 | in-del | -/T | 0.471768 | 0.115407 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602393 | GGTTTTCTGTTCCTG[-/T]TTTAGTTTGCTGAGA | 146845 |
| rs35656662 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9596486 | GCCTTGAAATTTTTA[C/T]ACAATTATTAATTCA | 146845 |
| rs35692348 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586134 | TTCCGTCAGACCGGG[-/G]AGTGAAGGACTCTGA | 146845 |
| rs35795512 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633402 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 146845 |
| rs35855599 | in-del | -/G | | | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576166 | AACACTAGATTGCGG[-/G]TGAGACTTGCACGCT | 146845 |
| rs35925268 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9600422 | AATTTTTGTATTTTT[-/T]AGTACAGACAGGGTT | 146845 |
| rs36018005 | snp | G/T | 0.00708563 | 0.0590983 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643027 | GACCAGATGGTCATT[G/T]CCACCTGAAAAAGAT | 146845 |
| rs36060092 | multinucleotide-polymorphism | GA/TT | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578595 | TGGAGTCTCGCTCTG[GA/TT]GTGTAATGGCACAAT | 146845 |
| rs36065034 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9641236 | CAGTGCTTTGGAGCA[C/G]AAGGGAAAGTTGGGA | 146845 |
| rs36124799 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581437 | GGAAAGATGTCAAAG[-/C]ATATATTAAGTATAA | 146845 |
| rs36182202 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595977 | CTAAAAAAACAAAAG[-/G]AAAAACTATATATAT | 146845 |
| rs55676181 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617043 | GCTTCAGACGATCAA[A/G]TTACTCTGAGCTACG | 146845 |
| rs55849704 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626933 | AAAATGTAGACATTG[C/T]TTGAGATGTACTGAA | 146845 |
| rs55862252 | snp | A/C | 0.32885 | 0.23724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584120 | CTGCCCTGTTCTTAC[A/C]AGGCTGGTCAGCCCA | 146845 |
| rs55966625 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9591226 | ATTTTTAGTAGAGAC[A/G]GGGGTCTCTTCATGT | 146845 |
| rs56001640 | snp | A/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596063 | TATATGTGTGTGTAT[A/G]TATATATATATATAT | 146845 |
| rs56024479 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625420 | CTGATCTCTAGCATT[A/G]TTAGCT | 146845 |
| rs56165620 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625470 | ACAGAGATTTGTGCA[A/G]TGTTTATAACCAGAA | 146845 |
| rs56169636 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604501 | AGCCGGGCGCAGTGG[C/T]TTGTGCCTGTAATCC | 146845 |
| rs56237272 | snp | A/G | 0.360632 | 0.224189 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607223 | TGATGGCGCATGCCT[A/G]TAATCCCAGCTACTC | 146845 |
| rs56238892 | snp | A/C | 0.183568 | 0.241012 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611409 | ATCCAGGATGGAGGG[A/C]AGGGATGAGATTGTG | 146845 |
| rs56258605 | snp | A/G | 0.142947 | 0.22592 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610106 | GTGGGGGAGAGGAAT[A/G]ATGAGAAACTTAACC | 146845 |
| rs56270741 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9625360 | GTTCTCTTGCCACTA[A/G]GATATTCCCCCTTTA | 146845 |
| rs56289163 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602595 | TAAACATACATGTGC[A/G]TGTAGAATGATTTAT | 146845 |
| rs56352557 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581210 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 146845 |
| rs56356021 | in-del | -/GAGA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597827 | AGAGAGAGAGAGAGA[-/GAGA]AAGAGAGAAAGAGAG | 146845 |
| rs56371689 | snp | A/G | 0.29278 | 0.246313 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637354 | CCTTAAAGCTGTTCC[A/G]TTGTGTAGCAGGAAT | 146845 |
| rs56404223 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631124 | CATAAGTCAGAATTT[A/G]CCATATTTAGGGCTC | 146845 |
| rs56408235 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590600 | TTTAAAAAACACTGA[C/T]GCCTGGGTCCCACCC | 146845 |
| rs56665510 | snp | A/G | 0.206642 | 0.246211 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631068 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs56749690 | in-del | -/C | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587016 | TCTGATCCTCTCCCT[-/C]CTCCCACCCTCCACC | 146845 |
| rs56818169 | in-del | -/AA/AAGAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631083 | AGAAAGAAAGAAAGA[-/AA/AAGAAA]GAAAGAAAGAAAGAG | 146845 |
| rs57052137 | in-del | -/T | 0.359152 | 0.224913 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584609 | CAGATTAATGCAGTA[-/T]TTTTTTTTTAATTTA | 146845 |
| rs57213820 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631004 | AAAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs57227334 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605351 | GTGGAAGATGCCAGT[C/T]TGAAAGACTGCACAC | 146845 |
| rs57323725 | snp | A/T | 0.115088 | 0.210473 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635139 | TTTGCATAGCAGGTG[A/T]CTGATTAAATTTCTC | 146845 |
| rs57409272 | in-del | -/T/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598216 | TTGTTTTTTTTTTTT[-/T/TT]ACATAGTGGGACAAT | 146845 |
| rs57510845 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631232 | CCTTTACCTTCTTAC[C/T]TGGAGCTCTTCCTCT | 146845 |
| rs57688684 | in-del | -/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597831 | GAGAGAGAGAGAGAA[-/G]AGAGAGAAAGAGAGA | 146845 |
| rs57881423 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636256 | AGAAAGAAAGAGAAA[-/AA]GAAAAATAACTAATG | 146845 |
| rs57960962 | snp | C/T | 0.0108618 | 0.0728899 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628711 | CTGTGCCAAGAAGGA[C/T]ATCAGGGTGTGGCAC | 146845 |
| rs57969608 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616359 | TCCTACGCCCACGGA[A/G]TCTCGCTGATTGCTA | 146845 |
| rs57975752 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629498 | CTTTCTTTCTTTCTT[-/T]TCTTTTCTTTCTTTC | 146845 |
| rs58055788 | in-del | -/AAAAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605718 | AAAAAAAAAAAAAAA[-/AAAAAA]TCAGTGCTTGCCATG | 146845 |
| rs58609679 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626421 | TTTTAGTAGATACAG[C/G]GTTTTGCCATGTTGG | 146845 |
| rs58770209 | in-del | -/TAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9604805 | AAATAAATAAATAAA[-/TAAA]AGAAGATATACAGAT | 146845 |
| rs58836715 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586586 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAAAGAAAA | 146845 |
| rs58955810 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9610532 | CCATTTTTTTTTTTT[-/T]GTTTGTTTTGAGATG | 146845 |
| rs59127471 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9583321 | ATTTGGCCATTTGAG[C/T]AAAAATAATCCATTT | 146845 |
| rs59210222 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628093 | AGTCTACCAAGACTT[G/T]GTGAGAATTTTAAAT | 146845 |
| rs59392801 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631677 | AGAGATGGCGGGGGT[C/T]GGGGGTCGGGCACAA | 146845 |
| rs59502035 | in-del | -/A | 0.48378 | 0.0885831 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609240 | AAAACATAAAAGATG[-/A]AAAAAAAAATCCCTG | 146845 |
| rs59716468 | in-del | -/A | 0.188 | 0.24219 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612800 | AGTCCCTGACTTATG[-/A]TTTTTTTTATTTTAT | 146845 |
| rs59948460 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606702 | ACACATATGTAGCTT[C/T]GAGGCGCTGTTGAAC | 146845 |
| rs59951986 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634587 | AGAGCGACATTTTGT[C/T]TCAAAAAAAGAAAAA | 146845 |
| rs60017435 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634721 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCCAGC | 146845 |
| rs60109261 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631108 | AAGAGAAAGAAAGAA[-/AA]CATAAGTCAGAATTT | 146845 |
| rs60552428 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627044 | ATATTACTTCTTCTT[A/C]TTATTTGAATTGGAA | 146845 |
| rs60584008 | in-del | -/AA/AAGA/AG | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636252 | AGAAAGAAAGAAAGA[-/AA/AAGA/AG]GAAAGAAAAATAACT | 146845 |
| rs60601081 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631097 | AGAAAGAAAGAAAGA[-/AA]GAAAGAAAGAACATA | 146845 |
| rs60641556 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631032 | AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 146845 |
| rs60833082 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634689 | GAATTGCTTGAATCC[A/G]TGAGGCAGAGGTCGC | 146845 |
| rs60945802 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631056 | AGAGAGAGAGAGAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs60980260 | snp | A/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9595897 | AAAAAGCTCTTTGTT[A/T]AAAAAAAAAAAGTTC | 146845 |
| rs60983584 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9639404 | CCACTGCACTCCAGT[C/T]TGGGTGACAGAGCAA | 146845 |
| rs61022707 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631002 | AAAAAAAGAAAGAAA[A/G]AAAGAAAGAAAGAAA | 146845 |
| rs61233470 | in-del | -/TCAAATATAC | 0.358728 | 0.225118 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584599 | CTCTTTTAGCAGATT[-/TCAAATATAC]AATGCAGTATTTTTT | 146845 |
| rs61407923 | snp | A/C | 0.117188 | 0.211804 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586318 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCTAGA | 146845 |
| rs61595466 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626861 | TATTTTTTGTTTTAA[C/T]TCTAAAGTGAGTAGG | 146845 |
| rs61617597 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628297 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGCCTAGC | 146845 |
| rs61686548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593865 | AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAATCG | 146845 |
| rs62064103 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577956 | AATTATCCGGGCGTG[A/G]TGGTAGGTGCCTGTA | 146845 |
| rs62064104 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9581190 | GGCGCGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 146845 |
| rs62064123 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596065 | TATGTGTGTGTATAT[A/G]TATATATATATATAT | 146845 |
| rs62064124 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617326 | AAGAAATGAGCAAAG[C/T]CTCCAAGAAATATGG | 146845 |
| rs62064128 | snp | A/G | 0.375 | 0.216506 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631040 | AGAAAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 146845 |
| rs62064129 | snp | A/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631044 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAAAGA | 146845 |
| rs62064130 | snp | A/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631048 | AGAGAGAGAGAGAGA[A/G]AGAGAGAAAGAAAGA | 146845 |
| rs62064131 | snp | A/G | 0.375 | 0.216506 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631052 | AGAGAGAGAGAGAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs62064132 | snp | G/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637555 | GGTACAGTATCTAAG[G/T]CAGGGGTTCTATTAT | 146845 |
| rs66835682 | snp | A/G | 0.401924 | 0.198543 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597010 | GGTGTGAGCCACTGC[A/G]CCTGGCCCTCCTCCT | 146845 |
| rs67008061 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9586569 | AGACTCCGTCTCAAC[-/A]AAAAAAAAAAAAAAA | 146845 |
| rs67062843 | snp | C/T | 0.291493 | 0.246533 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630379 | TGGACCTGATTTACA[C/T]AGCTGTGATTACAAG | 146845 |
| rs67110049 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638127 | CATGACATCTTGCTA[C/T]AGCTTTTATTTGTGA | 146845 |
| rs67561525 | in-del | -/AGAG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636250 | GAAAGAAAGAAAGAA[-/AGAG]AAAGAAAAATAACTA | 146845 |
| rs67700248 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635027 | GCTCTGGGTACTCAC[A/G]AACTTTCCTGACAGT | 146845 |
| rs67873669 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606396 | TCCAAAATACACACA[-/CA]CACACACACACGAAC | 146845 |
| rs71135995 | in-del | -/GT | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596062 | TATATGTGTGTGTGT[-/GT]ATATATATATATATA | 146845 |
| rs71135996 | in-del | -/AAAAAA/AAAAAAAA/AAAAAAAG/AAAAAAG | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598770 | GTTTCAAAAAAAAAA[lengthTooLong]GAAGAAAAAGTTCAC | 146845 |
| rs71358262 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579335 | CAATAGCGGGGGGCA[A/G]AGGAGGAAAAGTGGA | 146845 |
| rs71358265 | snp | G/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9621854 | CTCTGGGGACTGTGG[G/T]GGGGTCGGGGGAGGG | 146845 |
| rs71358266 | snp | A/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625990 | ATTGTTAAGGGCAAA[A/T]TTATGTACATCTATA | 146845 |
| rs71363714 | in-del | -/C | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580661 | ACCACTGCACTCCTG[-/C]CTGGGCAACAGAGTG | 146845 |
| rs71995451 | in-del | -/CTTT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9629475 | CTTTTCTTTCTTTCC[-/CTTT]CTTTCTTTCTTTCTT | 146845 |
| rs72046857 | in-del | -/A/AAAGA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636187 | AAAAAAGAAAGAAAG[-/A/AAAGA]AAAGAAAGAAAGAAA | 146845 |
| rs72458172 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9588788 | ATTTTTTTTTTTTTT[-/TT]TGAGATGGAGTTTCA | 146845 |
| rs72820024 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592869 | CATTTCTCTTGGATA[C/T]GAGGCACTTCTTTTG | 146845 |
| rs72820027 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603135 | AAATATCTGTCCAGC[A/G]AAGATGCTGGCTATC | 146845 |
| rs72820028 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605007 | TGGGAATGCAAAATA[A/G]TACGGCCACTTTGGA | 146845 |
| rs72820029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606707 | TATGTAGCTTCGAGG[C/T]GCTGTTGAACTCTTT | 146845 |
| rs72820034 | snp | C/G | 0.470608 | 0.117611 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613903 | ACGTTATTTCTAACA[C/G]TGAAAATGGCTGCTG | 146845 |
| rs72820038 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641909 | AACTCCCAGGCTAGA[A/G]GCAATTGGAAAAGAC | 146845 |
| rs73252165 | snp | C/G | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575149 | TCATGCAGTCCTTGG[C/G]ATTAACTGCTAAATA | 146845 |
| rs73253836 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587954 | GTTGAAATCACCTGG[A/G]CAGCTTTAGGGAATC | 146845 |
| rs73253847 | snp | A/T | 0.40157 | 0.198813 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592522 | TAGCAATCACTCTCC[A/T]TCCCTCCTCCTCCAA | 146845 |
| rs73253860 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597890 | AAGAAAAGAAAAAGA[A/G]GAAGACATTTAATAA | 146845 |
| rs73253863 | snp | G/T | 0.39527 | 0.203462 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598966 | CTATGCCACTGATGC[G/T]ATTTCTGCCACTGAA | 146845 |
| rs73253874 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604131 | CCTAGACACAGACCT[G/T]ATACCTTTCACAAAA | 146845 |
| rs73253879 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607486 | AGAGAATGGTGGGGG[A/G]CACCCCAACCTTTGA | 146845 |
| rs73253893 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622725 | AGTATAACATATATG[C/G]AAAATACATAAATCA | 146845 |
| rs73253895 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626765 | TGTCTCATTCCAGCA[C/T]TTACTCTTTCTAACT | 146845 |
| rs73253896 | snp | A/G/T | 0.0208652 | 0.0999875 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632859 | GCATATACTGATCCT[A/G/T]CCTGCCTTTTGTTTC | 146845 |
| rs73253897 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633212 | ATATTATAAATGTAT[A/G]CTTATTTTGAAATGG | 146845 |
| rs73253902 | snp | C/G | 0.103082 | 0.202275 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637202 | CATTTCTAAGAAGCT[C/G]CCAACTGAGAGTGCT | 146845 |
| rs73255705 | snp | G/T | 0.0640965 | 0.167152 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643923 | GACCTTGTGTCCTTG[G/T]GTATTAATCACCCAG | 146845 |
| rs73975736 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577308 | GAAGGTTTCTAAATG[A/T]TGAGGATTTCAGACC | 146845 |
| rs73975738 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587847 | CCTGTCCCCTCTAAT[A/G]TTCTCTCTTGGCCCG | 146845 |
| rs73975739 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592997 | TCCCACTGTGGAAAA[C/G]GGAGAATTTATGGCT | 146845 |
| rs73975740 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601463 | TCACCTCTTCAAAGC[A/G]TAGGGCCTATTGCTT | 146845 |
| rs73975741 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601614 | GCCTCAGCTGACATT[A/G]TAAGTCGTGAGCAAG | 146845 |
| rs73975743 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610141 | AATAGCAACAATCAG[A/G]AGAGGAAAGAAATAA | 146845 |
| rs73975744 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611818 | TTTTTAGGCAAATAT[C/T]CTATGAAGCTGATGT | 146845 |
| rs73975745 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611838 | GAAGCTGATGTTCCA[C/T]AGATCATTTAACTAT | 146845 |
| rs73975746 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612539 | TGCCAGGGCATTTAA[C/T]TTTATGAATGCATTT | 146845 |
| rs73975747 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613192 | GGTCTTCTAGATTTC[A/G]CAGGCTTCATGGTGG | 146845 |
| rs73975748 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614748 | ATTAAAGGATGTTTG[A/G]CAGCATTCCTGGGCT | 146845 |
| rs73975750 | snp | A/C/G | 0.0107246 | 0.0724382 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625129 | CAAGCAAACAAAAAA[A/C/G]CAACAAACAAAAAAC | 146845 |
| rs73975751 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625995 | TAAGGGCAAAATTAT[A/G]TACATCTATAGCTAC | 146845 |
| rs73975752 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629375 | TGCTCAGAAAGTACA[C/T]ATACTGCTTCACATC | 146845 |
| rs73975753 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630043 | ATCTTGGAGTCCTCA[C/G]TGCCTCCCCTTTTTC | 146845 |
| rs73975754 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630218 | CTTCTCTTCTCACCC[A/G]GTATACTTTCCCGCA | 146845 |
| rs73975755 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632671 | GAATTGAGGGTAATC[A/G]AGGAAGACTCAGGCT | 146845 |
| rs73975756 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632788 | TTCCTCCAGCACAGC[A/G]CCACTCACCAGGCCT | 146845 |
| rs73975757 | snp | C/T | 0.00188774 | 0.0306644 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633051 | ATTGAAAGCAGAAAT[C/T]TGAAAAAATAACGCT | 146845 |
| rs73975759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635203 | GTAGCATTTTTGAAG[C/T]TCTGTTGAAGATGAT | 146845 |
| rs73975760 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635258 | GCCCTTCAACTTAGC[A/G]TTCACACCCCACCCA | 146845 |
| rs73975761 | snp | G/T | 0.00968933 | 0.0689259 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635476 | ACACAAGTCATCAGT[G/T]TCCTGCATTAGGGTG | 146845 |
| rs73975762 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635735 | ATCGATGCTAGTGGG[A/G]AGGGTTACAATTTCC | 146845 |
| rs73975763 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636563 | TATTTTAGAATCGGA[C/T]GCCATTCCTCCACCC | 146845 |
| rs73975765 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637320 | TTATTTCTATGGATG[C/G]TTTGTGACTGCCTCA | 146845 |
| rs73975767 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639040 | GACTGGAGTAGAATT[C/G]CTGTGCCCAAACCGG | 146845 |
| rs73975768 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639889 | CCCAGGAGAGTGTCA[A/G]TTTGGCTTCTTTGGC | 146845 |
| rs73975769 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641934 | AAAGACAACAAAAGG[C/G]TCTCAAGGCAACTTG | 146845 |
| rs74252907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586245 | TTGCTGTCATGTTTG[C/T]AGAACCTGATCCGAT | 146845 |
| rs74266369 | in-del | -/TT | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9611255 | ATATACTTTTTTTTT[-/TT]AAGTTCATACTCATT | 146845 |
| rs74325896 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623488 | AACTCCATCAATGCA[A/G]TATTATAATTTTTGC | 146845 |
| rs74351852 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603727 | ATGACGGGTAATATA[C/G]ATGATGTAGATGACG | 146845 |
| rs74381681 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581635 | GAGTATGTCTGGAGA[A/G]GAGAGCAAAGAATAT | 146845 |
| rs74409753 | snp | C/T | 0.000478063 | 0.0154532 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585766 | ACTGTGAATCTCTCT[C/T]TTTTAGGACATGTGC | 146845 |
| rs74418047 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633675 | GAATTGTCATCTTAT[C/T]TTTTTTTTTTTTTTT | 146845 |
| rs74424345 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629101 | GTTCAATTTTGAAAA[A/G]GAGTTTGAAAAGGAC | 146845 |
| rs74432803 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630359 | GAGGCGTGAGCCACC[A/G]CACCTGGACCTGATT | 146845 |
| rs74823165 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629145 | GAGGACCCTTTTTGT[C/T]GTGTAAGAGATAAAA | 146845 |
| rs74857551 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597898 | AAAAAGAGGAAGACA[C/T]TTAATAAGCTCTGAT | 146845 |
| rs74863351 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638850 | CAGCCATGCCACTTT[G/T]GAAAGGCCATATCAC | 146845 |
| rs74899014 | snp | A/C | 8.23649e-05 | 0.00641683 | missense | CFAP52 | GRCh38.p7 | 17:9600171 | TGGGCCTGCGAAGGA[A/C]AAATTCAGTTTGGTG | 146845 |
| rs74941929 | snp | A/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642045 | AACATTTGCACAAGA[A/G]CCTTAAGAGCACAAA | 146845 |
| rs74982294 | snp | C/T | 0.122411 | 0.214991 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636407 | GGACCTCTTATGCTC[C/T]GAGCGTATCACACCC | 146845 |
| rs75043071 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579216 | CTAGCTCTAAAAAAA[A/G]GAGGGAGAGAGAGAA | 146845 |
| rs75224587 | snp | C/T | 0.267908 | 0.249358 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632792 | TCCAGCACAGCACCA[C/T]TCACCAGGCCTGCCT | 146845 |
| rs75235742 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9623346 | ACATCTCTTGAAACA[G/T]CATATACTTGGTTTT | 146845 |
| rs75250905 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611693 | ACTTATAAATAAAAT[G/T]TTGTATTCTAATTTT | 146845 |
| rs75305250 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598441 | GGATAGGAAAGTGGG[G/T]TATAGACATAGGGGA | 146845 |
| rs75305362 | snp | A/G | | | missense | CFAP52 | GRCh38.p7 | 17:9633026 | TCAGTGGCGGTGGGG[A/G]AGGGGAGGTATTGAA | 146845 |
| rs75387012 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637593 | AAAATCAACTGAAAT[C/G]CTGGTTTAAAATGCA | 146845 |
| rs75556393 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622978 | CTTTTAATGTAGTTA[G/T]TGTCATACAGATCTT | 146845 |
| rs75586838 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585217 | ATACAGAATCTCAAC[C/T]CCTTCTCAGACCTGA | 146845 |
| rs75671790 | snp | C/T | 0.00499432 | 0.0497214 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628669 | TTGATGGCTTCCTTG[C/T]AGTGGCACTGCTGAG | 146845 |
| rs75735851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584225 | GAATAAACTACCAAC[C/T]CAAGCAAAACAATAA | 146845 |
| rs75736950 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642758 | GTATACCAGTATACT[C/T]ATAGAGAAAAGACTG | 146845 |
| rs75742456 | snp | C/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642748 | TGATGTATATGTATA[C/G]CAGTATACTTATAGA | 146845 |
| rs75805385 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588283 | GACACTGTGCAGGTG[C/T]CCTGGCGCCCAGAGA | 146845 |
| rs75822418 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632427 | TTCTTGATCAAGAAG[A/T]TGACATAATTTTTAA | 146845 |
| rs75861018 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605694 | AGTGAGACTCCATCT[A/G]AAAAAAAAAAAAAAA | 146845 |
| rs75918522 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636585 | CCTCCACCCCTCTCC[C/T]CACCCACCTATCACC | 146845 |
| rs75942703 | in-del | -/GAGA | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581517 | AGTGTACATATGTTT[-/GAGA]GAGAGAGAGGGGATA | 146845 |
| rs75953015 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583047 | ACTTTTGTACACACT[A/G]TCTTGTTTTTCACAT | 146845 |
| rs75992562 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583988 | AAAGACCACCTCACC[A/G]AGTTGAGTCTCTGAA | 146845 |
| rs76048087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593203 | ATTTAACATAACGCC[C/T]CCTCCCCAGCATTTT | 146845 |
| rs76110934 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640558 | ACTCCATCCATGTCC[C/T]GGCAAAGGACATGAT | 146845 |
| rs76282985 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632396 | ATAAGCCTTTTTTTT[A/T]AAATAAAAAAGGAAG | 146845 |
| rs76441977 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641039 | AGCATTCTTTCCTAA[A/G]AAGGAAATTTAAATC | 146845 |
| rs76491800 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592075 | TCATAAAATTGACCC[A/G]TGTTAAGGTGTACAG | 146845 |
| rs76532160 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612800 | AGTCCCTGACTTATG[A/T]TTTTTTTTATTTTAT | 146845 |
| rs76627895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625624 | CACCTTTTTCTACAG[C/T]CACCATAGCTGTGGG | 146845 |
| rs76635578 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588746 | CTCCTTCCATACCCA[A/G]TAGAATATTTTTTAG | 146845 |
| rs76653197 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623566 | TAAAATGTCTTGTGT[A/G]CTTACTTATATATTT | 146845 |
| rs76725051 | snp | A/G | 0.0337553 | 0.125452 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576415 | TTACTAAGAAGTCAC[A/G]GACTCTACACAAGGG | 146845 |
| rs76785413 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631580 | CTTGGTGGATTTGAG[A/G]AATAGCAAGAGGGCC | 146845 |
| rs76808591 | snp | C/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614160 | TTTTCTTTCTTTCTT[C/T]TTTTTTTTTTTTTTG | 146845 |
| rs76883105 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578114 | AAATAAATAAATAAA[C/T]AAACAAACATACATA | 146845 |
| rs76978598 | snp | C/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603183 | TTGGCACTTAAGTCA[C/T]CTGTGGATGCTGAAA | 146845 |
| rs77002268 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590867 | CTGGATAGTCTCTGT[G/T]GTGAGAAGGGTGGAG | 146845 |
| rs77071429 | in-del | -/AAAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589750 | AAAAAAAAAAAAAAA[-/AAAAA]GAAAAGAAATGTATC | 146845 |
| rs77138371 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602243 | TAACCCGTCGTCTAC[A/G]TTAAGTATTTCTCTT | 146845 |
| rs77186622 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594754 | CATGTAAAATAATTA[C/T]GGGCAGGATCAGCTT | 146845 |
| rs77241553 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638945 | GATTAAAGTCATGCT[C/T]GCTCATGGTGCTTAT | 146845 |
| rs77262593 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579067 | CTTTGTCCAAAAGGG[A/G]ATCTGTTCAGTCAGT | 146845 |
| rs77377585 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634506 | AAAAATTAGGCCAGG[C/T]GTGGTGAGTTGGAGG | 146845 |
| rs77377854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598698 | CCTGGGAGGCGGAAG[C/T]TGCGGTGAGCTGGCA | 146845 |
| rs77404941 | snp | A/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605720 | AAAAAAAAAAAAAAA[A/T]AAATCAGTGCTTGCC | 146845 |
| rs77424298 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633676 | AATTGTCATCTTATC[C/T]TTTTTTTTTTTTTTT | 146845 |
| rs77481032 | snp | A/C/G | 0.0325976 | 0.123435 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628941 | TCCCACTGTCCACCC[A/C/G]CTTCTTGCTTCTAAT | 146845 |
| rs77515080 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603867 | CACAATATTGAAGAA[A/G]AACACAGTTGGAGGA | 146845 |
| rs77537820 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577305 | AAGGAAGGTTTCTAA[A/G]TGATGAGGATTTCAG | 146845 |
| rs77609838 | snp | C/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642082 | CCAAGACTTAGATTG[C/G]TAGGCTTGCTATTTT | 146845 |
| rs77686457 | snp | A/G | 0.128632 | 0.218563 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609702 | ACAGAACGAGACCTC[A/G]TCTCAATTTTTTTTT | 146845 |
| rs77771659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601517 | CCAGCCCCATTGCCA[C/T]ACATAAGAGAAGTGT | 146845 |
| rs77817088 | snp | G/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596732 | TGTGTGTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 146845 |
| rs77839011 | snp | C/T | 0.0100184 | 0.0700629 | missense | CFAP52 | GRCh38.p7 | 17:9594243 | TCTGTGGCAGCCCTG[C/T]AGCCGGCCTCAATGT | 146845 |
| rs77840450 | snp | C/T | 8.23839e-05 | 0.00641757 | missense | CFAP52 | GRCh38.p7 | 17:9635514 | ACAACGAGGAGTGTG[C/T]CACCGCCAGCACCGA | 146845 |
| rs77945520 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587905 | AAGCCTCTGAGAAAA[A/G]TACCATAAAAGTGGT | 146845 |
| rs77954781 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626741 | GGCAAGAAGCCCCAT[C/T]ACATCTGTTGTCTCA | 146845 |
| rs78005280 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590182 | CTTCAGAGCAGGTGG[C/T]GCAGAATCCTCATTC | 146845 |
| rs78027461 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579332 | CAGCAATAGCGGGGG[A/G]CAGAGGAGGAAAAGT | 146845 |
| rs78179016 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638948 | TAAAGTCATGCTTGC[C/T]CATGGTGCTTATAGC | 146845 |
| rs78189361 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631028 | AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA | 146845 |
| rs78233327 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583191 | AGAAAACTATAAAAA[A/G]TTTTTAGTAGGAATA | 146845 |
| rs78246223 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631016 | AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs78261387 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613976 | CTTTTGGTCTCACTT[C/T]TTCCCCTCTTTTTTT | 146845 |
| rs78267939 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603520 | GGCCCTAAGTAGATA[C/T]TTCATGTTCATGGAT | 146845 |
| rs78350111 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635753 | GGTTACAATTTCCAG[A/G]AAGAACTGAATGTTA | 146845 |
| rs78394376 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9636246 | GAAAGAAAGAAAGAA[A/G]GAAAGAGAAAGAAAA | 146845 |
| rs78430112 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610065 | CTCTTAATTTACAAC[C/G]GAACCTGAATCCTAA | 146845 |
| rs78477371 | snp | A/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577266 | AGCAACCCCCTGAGG[A/G]GATGTTGTTGGTCCT | 146845 |
| rs78608879 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576490 | TCCAGAGAAATAGCA[A/C]AAAAAAAAAGAAGAG | 146845 |
| rs78775270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629784 | TAGTAAAAACGGGTT[C/T]TCACCATGTTGGCCA | 146845 |
| rs78840286 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608458 | GGGACACTGCCCATT[G/T]AATAAATACATAAGT | 146845 |
| rs79055608 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600975 | GAAGAAAGTCATTGG[C/T]GGCACTATTCACAAT | 146845 |
| rs79115297 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9635039 | CACGAACTTTCCTGA[C/T]AGTACCAGAAATTTG | 146845 |
| rs79130013 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639995 | TCTATCTCTTTAGGC[A/G]TTTACTATGAAATCA | 146845 |
| rs79133731 | in-del | -/T | 0.413582 | 0.189052 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632078 | GCGCCCAGCCTCCAC[-/T]TTTTTTTTTCTTTTT | 146845 |
| rs79165165 | snp | A/T | 0.41441 | 0.188333 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589747 | CAAAAAAAAAAAAAA[A/T]AAAAAAAGAAAAGAA | 146845 |
| rs79173501 | snp | A/C | | | missense | CFAP52 | GRCh38.p7 | 17:9635516 | AACGAGGAGTGTGTC[A/C]CCGCCAGCACCGATG | 146845 |
| rs79224292 | snp | A/C | 0.136166 | 0.22258 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614674 | GCCAGGATTTCTCAA[A/C]CTCCGCACTATTGAC | 146845 |
| rs79234052 | in-del | -/G | 0.428484 | 0.175052 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603153 | ATGCTGGCTATCTTA[-/G]GGTTTCTCAAACCTT | 146845 |
| rs79276762 | snp | C/T | 0.0711525 | 0.174681 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642846 | GATTTTACCTCTTTG[C/T]ATTTCCCCCTCCTCT | 146845 |
| rs79401267 | snp | C/T | 4.95135e-05 | 0.00497537 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643078 | GGGTGAAGTGACTCA[C/T]GTTGGGGTGGGACAC | 146845 |
| rs79408319 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586124 | ACCCATTTTCATTCC[G/T]TCAGACCGGGAGTGA | 146845 |
| rs79441288 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579389 | CGGCAAATAGCTTGG[G/T]GTGGCTTCAGTATCA | 146845 |
| rs79517082 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615342 | ATTCATTACAGAGAC[G/T]TGCATTGCAGCAAAA | 146845 |
| rs79523782 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9606241 | TTTTAAAAATTAGCC[A/G]GCGTGGTGGCATGCA | 146845 |
| rs79561054 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632338 | GACTCAAGCAATCCA[C/T]CCACCTTGGCCTCCC | 146845 |
| rs79577119 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606534 | GTACCATTTTCATCC[A/C/T]TGCTTTACAGATGAG | 146845 |
| rs79600226 | snp | A/T | 0.0283406 | 0.115616 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643837 | AAGAAAGATGAAATT[A/T]CAGAGATGCTTTATT | 146845 |
| rs79772539 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626634 | GAGGAGGAGCTCATT[C/T]ACCAAAGGCATTATC | 146845 |
| rs79792561 | snp | G/T | 0.397271 | 0.202018 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601183 | AACCAAACACCACAT[G/T]TTCTTACTCATAGGT | 146845 |
| rs79811592 | snp | C/T | 0.137867 | 0.223442 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640019 | GAAATCAGAACTTTT[C/T]TGTTAACATGATCAA | 146845 |
| rs79857679 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605697 | GAGACTCCATCTGAA[A/G]AAAAAAAAAAAAAAA | 146845 |
| rs79997125 | snp | A/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642113 | TGGTGGGCATTGATA[A/T]TAGAAATGGGGCCTT | 146845 |
| rs80013522 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606492 | TAAATGATCTCATTC[A/G]ATCTTCATAAACGCC | 146845 |
| rs80018635 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578346 | TGGCCAGAGGTAGTC[C/T]GTGGTGAGTGGTCTT | 146845 |
| rs80058914 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632307 | GCCATGTTTCCAGGC[C/T]GGTCTTGTGCTCCTA | 146845 |
| rs80068515 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599564 | TTCCTCCCATTCTAT[A/G]TGTAGCCCTTACCCT | 146845 |
| rs80102768 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622852 | ACTACCCTCACCCTC[C/T]TACTTACTACCTGAA | 146845 |
| rs80162461 | snp | C/T | 0.0283406 | 0.115616 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643320 | CTTGAGTCAATTTTT[C/T]TCTTTTTCTTTATAG | 146845 |
| rs80196528 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601621 | CTGACATTATAAGTC[A/G]TGAGCAAGACCTAGA | 146845 |
| rs80270466 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590102 | GTTTTTTGAATACAT[A/T]CCCCTCCACCTTCAG | 146845 |
| rs80349882 | in-del | -/TTC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640242 | TTTTTTTTTTTTTTT[-/TTC]AACTTTAAGTTCAGG | 146845 |
| rs111234685 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605216 | TTCAGTAAGTAAAGG[A/G]ATACGTAAACTGTGA | 146845 |
| rs111264100 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615765 | AGGCATGTACCACCA[C/T]GCCCAGCTAATTAAA | 146845 |
| rs111293659 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639355 | AGAATTGCTTGAACC[C/T]GGGAAGTGGAGGTTG | 146845 |
| rs111296370 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642496 | GGGCGTGGTGGTGCA[C/T]GCCTATAATCCCAGC | 146845 |
| rs111298334 | in-del | -/AT | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640441 | GTGTTGTTTCCCCAC[-/AT]GTGTCCATCTCTTTT | 146845 |
| rs111306169 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627742 | TTTTAGAGGCAAATT[A/C]TCTTGTCTCACTCTG | 146845 |
| rs111325132 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588570 | TCTGCTCATCTACCC[A/G]CTCACCTCGGACTTC | 146845 |
| rs111389188 | snp | A/C/G | 0.0240643 | 0.107019 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607793 | GGAAGGATGGTGAAG[A/C/G]CTGTTTGCATCCTGT | 146845 |
| rs111402724 | snp | C/G | 0.0364509 | 0.129988 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575377 | TGAACCTCGGTTTCT[C/G]CACCTGTGAAATAAG | 146845 |
| rs111476097 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610840 | CACCATGCCCAGCCT[A/G]TTCTTCCCCTTTTAT | 146845 |
| rs111478468 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640953 | CCAGCTGGCCGTATC[C/G]CATTTTCTTTATGCA | 146845 |
| rs111500361 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574673 | CCGAGTAGCTGGGAT[C/T]ACAGGCATGTACTAC | 146845 |
| rs111562397 | in-del | -/T | 0.402982 | 0.197728 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610531 | TCTTTCCTTTCCCCA[-/T]TTTTTTTTTTTTGTT | 146845 |
| rs111578073 | in-del | -/C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632077 | GCGCCCAGCCTCCAC[-/C/T]TTTTTTTTTTCTTTT | 146845 |
| rs111592407 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610621 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 146845 |
| rs111629803 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631827 | GCTGGGAGTGCAGTG[C/G]TGTGATCTCGGTTCA | 146845 |
| rs111638739 | snp | G/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590260 | TACCTATGCCCATGT[G/T]CCTGCCCTTCTGGCG | 146845 |
| rs111653153 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9618731 | ACATGGAAACTGAAC[A/C]ACCTGCTCCTGAACG | 146845 |
| rs111658414 | snp | A/G | 0.031825 | 0.122064 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575710 | AGGCCACCAGCGGCA[A/G]TGCGAAGTGATTGCC | 146845 |
| rs111670697 | in-del | -/CATTG | 0.103082 | 0.202275 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634544 | GAGCCGAGACCACGC[-/CATTG]CATTGCACTCCAGCC | 146845 |
| rs111721616 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596707 | CCTCCTCATGGTTGT[C/T]GTGTGTGTGTGTGTG | 146845 |
| rs111758052 | snp | A/G | 0.031825 | 0.122064 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578481 | GTTGCAGTTGTTTTC[A/G]TATTGCTTATCTCAA | 146845 |
| rs111784998 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640696 | TGGAGTGCAGTGGCA[C/T]AATCTCAGCTCACTG | 146845 |
| rs111846590 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605710 | AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAATC | 146845 |
| rs111872249 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594996 | CCCGGGTTCAAGCAA[A/T]TCTCCTGCCTCAGCC | 146845 |
| rs111914194 | snp | C/T | 0.00157238 | 0.0279949 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638577 | TAGGGAAGAGAAAGT[C/T]GACTTTCACAGCTTT | 146845 |
| rs111922315 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582752 | AGCGATTCTCCTGCC[C/T]CAGCCTCTCAAGTAG | 146845 |
| rs111932348 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9616708 | TGACCCCCGGGCAGC[A/C]TAACTGGGAGGCACC | 146845 |
| rs111932926 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603156 | GCTGGCTATCTTAGG[G/T]TTCTCAAACCTTTGG | 146845 |
| rs112013930 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642687 | CAAGTACATTGACTA[C/T]AAAGCAGGTATCAAA | 146845 |
| rs112017923 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606310 | ATTGCTTCATCCCGG[A/G]AGTTCGTGGTTACAG | 146845 |
| rs112021263 | in-del | -/TGA | 0 | 0 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577309 | AAGGTTTCTAAATGA[-/TGA]GGATTTCAGACCAGG | 146845 |
| rs112097194 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612620 | TGGTGAATTATTTTA[A/G]GAGACTTTCCATTGT | 146845 |
| rs112138345 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600563 | ACACACTTTGTTTGT[G/T]TGTTTGTTTGTTTGT | 146845 |
| rs112179867 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575700 | TCATCCCGAAAGGCC[A/G]CCAGCGGCAATGCGA | 146845 |
| rs112258380 | snp | C/G | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641511 | TCAGCACATCAACAT[C/G]TCTTTAAATAGAATG | 146845 |
| rs112270562 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630312 | GGCCAGGCGCGGTGG[C/T]TCACGCCTGTAATCC | 146845 |
| rs112280734 | in-del | -/CTC | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634144 | TTTTTCTCTGGTTCT[-/CTC]CTCCTCTGTGCCCCA | 146845 |
| rs112283605 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591742 | AAATGAGCCAGGCAC[A/G]GTGGTGTGTGCCTGT | 146845 |
| rs112312923 | in-del | -/C | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629500 | TTCTTTCTTTCTTTT[-/C]TTTTCTTTCTTTCTT | 146845 |
| rs112346431 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635908 | TCGGGCGTGGTGGCT[C/T]CTGCCTGTAATCCCA | 146845 |
| rs112355144 | snp | A/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594940 | GTGTCACCCAGGCTG[A/T]AGTGCGGTGGCATGA | 146845 |
| rs112431705 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629329 | TTTCTCAGTATTGTC[A/T]TATGCTAAATCTATC | 146845 |
| rs112439825 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640292 | TGCAGGTTTGTTCCA[C/T]AGGTAAACATGTGCC | 146845 |
| rs112446338 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637000 | CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA | 146845 |
| rs112448825 | snp | A/C | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598829 | GTCAGGGAAGAGTCA[A/C]CTAGACACAGCACAG | 146845 |
| rs112474080 | in-del | -/A | 0 | 0 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576490 | CCAGAGAAATAGCAC[-/A]AAAAAAAAAGAAGAG | 146845 |
| rs112518826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608899 | AAGGTATGTACACAC[A/G]AAAGAAGTCACTACC | 146845 |
| rs112525792 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626467 | ACTCCTGACCTCAGG[G/T]GATCCACTCACCTTG | 146845 |
| rs112525953 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634295 | GGCACTATAAGAAGG[C/T]GTAAGCATCTGACTA | 146845 |
| rs112544398 | snp | A/G | 0.000823628 | 0.0202765 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585916 | GTCTCCTGCTTGGCC[A/G]TCTCCAGGTCTGGAG | 146845 |
| rs112604590 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627247 | GGGCACAGTGGCTCA[C/T]ACCTGTAATCCCAGC | 146845 |
| rs112610193 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623188 | TTTATTAAAGTGTTC[C/T]TCTTTGTCTCTAGTA | 146845 |
| rs112612589 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612285 | TTGAGTGAATCTACT[C/T]TACTTTTGTGCTTCT | 146845 |
| rs112644163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586362 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAGCCA | 146845 |
| rs112696029 | in-del | -/TTTG/TTTGTTTG | 0.0126979 | 0.078662 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623670 | CTTTGCTTAGCTTTT[-/TTTG/TTTGTTTG]TTTGTTTGTTTGTTT | 146845 |
| rs112783393 | snp | C/T | 0.00154819 | 0.0277795 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643107 | ACAGTGGCAACATCA[C/T]ACGCATCCGCATAAG | 146845 |
| rs112816088 | snp | A/G | 0.0314385 | 0.121371 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575911 | CCGTGCGCGACCGGA[A/G]CCTGGAGTTTGCAAA | 146845 |
| rs112927879 | snp | A/T | 0.0283406 | 0.115616 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | CFAP52, USP43 | GRCh38.p7 | 17:9643418 | CTAATTAGAACTTTT[A/T]ACATTTTGAATAAAT | 146845 |
| rs112931080 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631683 | GGCGGGGGTTGGGGG[G/T]CGGGCACAAATACTA | 146845 |
| rs112964538 | in-del | -/T | 0.0285824 | 0.116079 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632255 | GCAAGTTTTTTTTTG[-/T]TTTTTTTTTTCATAT | 146845 |
| rs113007203 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615638 | TTTTTTTTCTTTTAG[C/G]ACATAAGGTCTTCCT | 146845 |
| rs113018738 | in-del | -/A | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635296 | CAAAGACAGGGAATT[-/A]AAAAAACACAAATCA | 146845 |
| rs113052016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611192 | TTCTTCATTGTCTAA[A/G]CTAAACTAGTTACAG | 146845 |
| rs113066379 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589720 | CCTGGGGACAAGAGC[A/G]AGACTCCGTCTCAAA | 146845 |
| rs113082866 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640359 | GTATTAAGCCCTGCA[G/T]GCATTAGCTATTCTT | 146845 |
| rs113085321 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636103 | CGCTTGAACCCAGGA[C/T]GCGGAGGTTGCAGTG | 146845 |
| rs113095667 | snp | C/T | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599834 | GCAACCTCTGCCTCC[C/T]GAGTTCAAGCGATTC | 146845 |
| rs113106614 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609092 | TTATGGCCTCTGCTA[C/T]CCCCAGGAAGCCAGG | 146845 |
| rs113139431 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597342 | CGTAATATATTGTAT[A/G]CTTGAAAATTGCTAA | 146845 |
| rs113164874 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9620946 | ACATAGGCATGGGCA[A/C]GGACTTCATGTCCAA | 146845 |
| rs113172662 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634478 | GGCCAAACCCTGTCT[C/G]TACTAAAAATACAAA | 146845 |
| rs113215689 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632244 | CACCATGCGAGGCAA[A/G]TTTTTTTTTGTTTTT | 146845 |
| rs113220597 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622731 | ACATATATGCAAAAT[A/G]CATAAATCATAAATA | 146845 |
| rs113302651 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639877 | CTACTGGGGCTGCCC[A/G]GGAGAGTGTCAATTT | 146845 |
| rs113311384 | in-del | -/AGAAG/AGAAGAAG | 0.0020016 | 0.031572 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622552 | TTCTATTAAAAAAAA[-/AGAAG/AGAAGAAG]AAGAAGAAGAAGAAG | 146845 |
| rs113352875 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640289 | ATGTGCAGGTTTGTT[C/G]CATAGGTAAACATGT | 146845 |
| rs113395932 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579648 | TCTCAGCTCACTGCA[A/C]CCTCTGCCTCATGGG | 146845 |
| rs113409503 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623110 | TTTTTGTTTTGCATA[C/T]CTTAAAGCTCTGTTA | 146845 |
| rs113440291 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614672 | AGGCCAGGATTTCTC[A/G]ACCTCCGCACTATTG | 146845 |
| rs113468616 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633321 | GCGATTCTCCTGCCT[C/T]AGCCTCCTGAGCAGC | 146845 |
| rs113471796 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586455 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGACAG | 146845 |
| rs113537068 | snp | C/T | 0.427575 | 0.175975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630581 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 146845 |
| rs113544023 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637013 | TCGCACCACTGCACT[C/T]CAGCCTGGGCCACAG | 146845 |
| rs113548600 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643008 | CAATGCCATATACGT[A/G]TTTATCTTTTTCAGG | 146845 |
| rs113556452 | in-del | -/TT | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640225 | CCTGGTCAAGCACTC[-/TT]TTTTTTTTTTTTTTT | 146845 |
| rs113570158 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575784 | CGCCGCCCTCACCCG[A/G]GACTCACCAGGGGTC | 146845 |
| rs113576151 | snp | A/T | 0.000713865 | 0.0188792 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628693 | TGCTGAGCTATTTGC[A/T]ACCTGTGCCAAGAAG | 146845 |
| rs113595843 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584602 | CTTTTAGCAGATTAA[C/T]GCAGTATTTTTTTTT | 146845 |
| rs113605539 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629837 | TCAGGCAATCCACCC[A/G]CCTCGGCCTCCCAAA | 146845 |
| rs113633622 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626426 | GTAGATACAGCGTTT[A/T]GCCATGTTGGCCAGG | 146845 |
| rs113651658 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634718 | GCAGTGAGCCGAGAT[C/T]GCGCCATTGCACTCC | 146845 |
| rs113680739 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637081 | AACAAACAAAAAAGC[-/A]AAAAAAAACCCGACA | 146845 |
| rs113686931 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632110 | TGAGACAGGGTCTTG[C/T]TCTGTTGCCCAGGCT | 146845 |
| rs113738245 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640848 | AGGGTTTCACCATAT[C/T]GCCCAGGCTGGTCTC | 146845 |
| rs113749938 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587808 | TTATTTTCTGCAAGG[C/T]GTATTTCCAGAAGTG | 146845 |
| rs113755446 | in-del | -/C | 0.0551013 | 0.156571 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592539 | CCCTCCTCCTCCAAG[-/C]CCCAGGCAACCACTA | 146845 |
| rs113779067 | snp | A/C | 0.0360663 | 0.129354 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574693 | GCATGTACTACCATG[A/C]CCGGCTAATTTTGTA | 146845 |
| rs113801746 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615455 | TTTAATTCATTCATA[A/C]GTATTACTATCTGAT | 146845 |
| rs113811909 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613607 | ACTGCAACCTCTGCC[C/T]CCTCGATTCAAGCGA | 146845 |
| rs113879411 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581186 | GCCGGGCGCGGTGGC[C/G]GGCACCTGTAGTCCC | 146845 |
| rs113881919 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626995 | CAAGCTAGAAATTTA[C/T]ACTTATGAACCAAAT | 146845 |
| rs113988991 | snp | A/G | 0.5 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585419 | CACACCTGTAATCCC[A/G]GCACTTTGGGAGGCT | 146845 |
| rs114114423 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588364 | AGGACACAGCTCAGC[C/T]CGCTCGTGCCCAGAG | 146845 |
| rs114163639 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580853 | GTTGAAGGCCAGTTT[C/T]ATAGTATCTATTACA | 146845 |
| rs114250092 | snp | C/T | 0.135825 | 0.222405 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623691 | TTGTTTGTTTGTTTG[C/T]TTGTTTGTTTAAGAG | 146845 |
| rs114378209 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633659 | AGGATCGTGGTTGTA[C/T]GAATTGTCATCTTAT | 146845 |
| rs114467025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581785 | CATATTTTCTCTCCT[A/G]ATTCCTTGGCAGCCA | 146845 |
| rs114593009 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633357 | TTACAGGCGCACACC[A/G]TCATGCCCAGCTAAT | 146845 |
| rs114602679 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630768 | GAGATGGGGTTTCGC[C/T]TGAGGTCAGGAGTTT | 146845 |
| rs114828427 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624107 | GTTTATATTTCAATA[C/T]TTTTTCTTTGCTTTT | 146845 |
| rs114949599 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588822 | TTGTTGCCCAGGCTG[C/G]AGTAATGGCACAATC | 146845 |
| rs115025791 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609083 | ACATGTGCTTTATGG[C/T]CTCTGCTACCCCCAG | 146845 |
| rs115341323 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633660 | GGATCGTGGTTGTAC[A/G]AATTGTCATCTTATC | 146845 |
| rs115377020 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642614 | GAGTGACAGACAGTC[C/T]GTCTCAATAAATAAA | 146845 |
| rs115389354 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592047 | TTTTTTTAATTGAAA[C/T]ACATTTCACATATCA | 146845 |
| rs115421145 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598091 | TGGTGTTATGAGGAT[C/T]GAATAAAAGATCTTT | 146845 |
| rs115493968 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633601 | TTAAGGAATTCATGC[A/G]GGTGTTTTGCCAGTG | 146845 |
| rs115543110 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578210 | AAACATTGATGTAAT[A/C]TATCACTCATATTCA | 146845 |
| rs115613569 | snp | G/T | 0.00953873 | 0.0683987 | downstream-variant-500B, upstream-variant-2KB, intron-variant | CFAP52, USP43 | GRCh38.p7 | 17:9643758 | ATTCCTGACAGGGTA[G/T]AGAGAAATATGCATG | 146845 |
| rs115633434 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632267 | TTGTTTTTTTTTTTC[A/G]TATTTTTTGTAGAGA | 146845 |
| rs115677604 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624626 | ATGTATTTTAAAATA[G/T]CTGCTTTAAAGTTTT | 146845 |
| rs115740131 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580548 | CCAAAAAATAGCCAG[G/T]CATGGCGATGCATGC | 146845 |
| rs115742045 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611077 | ACTGAGGTTTAACTT[G/T]TCATCTTCCTTTCGT | 146845 |
| rs115799119 | snp | C/G/T | 0.00662509 | 0.057177 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575803 | TCACCAGGGGTCCGG[C/G/T]GCCATCCTGCAGACT | 146845 |
| rs115922623 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598052 | TCTAATTTGGGAGGG[A/G]GGATCATAAAACCTG | 146845 |
| rs115931305 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637299 | ACTAGAAGGACATGT[C/T]TGAACTTATTTCTAT | 146845 |
| rs116050907 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633650 | TTTCCTCCGAGGATC[G/T]TGGTTGTACGAATTG | 146845 |
| rs116153083 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625087 | TCCAAGCTGAGCTCA[G/T]TTGGGGAATGTATTT | 146845 |
| rs116275977 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606904 | CTTGAGCCTTGGTTT[A/C]TCTTCTCAATCACAA | 146845 |
| rs116522211 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633150 | TCAAGCAGGACCAAA[C/T]TGACATTTTGATGAG | 146845 |
| rs116586188 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596487 | CCTTGAAATTTTTAT[A/G]CAATTATTAATTCAG | 146845 |
| rs116587543 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605465 | ACCACTAATCCCAGC[A/G]CTTTGTGGGGAGCTG | 146845 |
| rs116710896 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588972 | GCCAGGCATAGTGCC[A/G]GGGCCTGTAATCCCA | 146845 |
| rs116815948 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580938 | TTTTCAAAAAATTTA[C/T]GTGCAATGAAGTTCA | 146845 |
| rs116952958 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586281 | GAAAAGTGATAGAGC[A/G]GGCTGGGCGCGGTGG | 146845 |
| rs117068078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601996 | TCATTTAATATTCAA[A/G]CATTCAAGGAGATGC | 146845 |
| rs117334935 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578979 | CCACAAAAGAGAGGG[G/T]GTATAATGAGGCATG | 146845 |
| rs117569464 | snp | A/C | 0.000296609 | 0.0121744 | missense | CFAP52 | GRCh38.p7 | 17:9628789 | CTGCCACGGCATCGA[A/C]TTCATGAGGGACGGC | 146845 |
| rs117620514 | snp | A/T | 0.0337553 | 0.125452 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576363 | CGCCTGATTACATAT[A/T]TTTTAAATGCCATTC | 146845 |
| rs117638439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595657 | TTTTATATTAAAAAA[A/G]AAGTTTTTTTAGGAC | 146845 |
| rs117742036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615271 | GAAACTTGTGTAATA[C/T]TCTGTTAGGTTGGTG | 146845 |
| rs117901126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612201 | TCACTTCTGTGAGGG[C/T]GTGTCTGAAATTATA | 146845 |
| rs117945544 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605944 | GTTTATTAGCTGTCA[C/T]ACATCTACTCTGCTG | 146845 |
| rs118086550 | snp | C/T | 0.0283818 | 0.115695 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575837 | CCCGCCGCTCGGACT[C/T]TTCCTGCTCTTAGCA | 146845 |
| rs118154450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639054 | TGCTGTGCCCAAACC[A/G]GTTATCACTTTGACT | 146845 |
| rs137866064 | snp | G/T | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574670 | CTCCCGAGTAGCTGG[G/T]ATTACAGGCATGTAC | 146845 |
| rs137875006 | in-del | -/GA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609991 | GGAATCTGATTTCTG[-/GA]GAGAGAGAGAGAGAG | 146845 |
| rs137995073 | snp | C/T | 0.00433466 | 0.0463523 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608169 | TTTGTTGGTGGGCTC[C/T]GGAGCCGGACTGCTG | 146845 |
| rs137996810 | snp | C/T | 3.29826e-05 | 0.00406082 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9638687 | TGAGGAGTTCCAGAT[C/T]ATCACCAGCGGAACA | 146845 |
| rs138015662 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579859 | AGGCGTGAGCCACTG[C/T]GACTGGCCTTAAACT | 146845 |
| rs138018844 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642515 | TATAATCCCAGCTAC[C/T]TGGGAGGCTGAGACA | 146845 |
| rs138116556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613044 | GTTCAGTAGGTGAAG[C/T]GTATTAAGTGCATTT | 146845 |
| rs138124935 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640262 | CTTTAAGTTCAGGGG[C/T]ACATGTGCAGGATGT | 146845 |
| rs138128293 | in-del | -/A | 0.084364 | 0.187256 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622663 | CCCTCAGACTTGAAT[-/A]ACAGTTTGGTGCAGT | 146845 |
| rs138149905 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625082 | TGCCATCCAAGCTGA[A/G]CTCAGTTGGGGAATG | 146845 |
| rs138276250 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628375 | ACCTTTGCCTTCCAG[G/T]TTCAAGCGATTCTCC | 146845 |
| rs138342063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595279 | CCCATCTTGGAAAGG[C/T]ACACATGGTTGGTTA | 146845 |
| rs138429217 | snp | A/G | 0.00016685 | 0.00913221 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643173 | ATGGAGCCATTTTGC[A/G]ATGGAAGTACCCATA | 146845 |
| rs138470663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597463 | TGTATATGTATATAA[A/G]CATCATGATGTACAC | 146845 |
| rs138663544 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642275 | TACCACACAACATGC[C/T]GATTGGAACATCATT | 146845 |
| rs138715665 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639403 | ACCACTGCACTCCAG[A/T]CTGGGTGACAGAGCA | 146845 |
| rs138717268 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584707 | GCTCACTGCAACCTC[C/T]GCCTCGTGGGTTCCA | 146845 |
| rs138750173 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624422 | CAGTTTACAGATTTT[C/T]CACCATCTCCAATCT | 146845 |
| rs138750181 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580614 | GGATCACCTGAGCCC[A/G]GGAGGTAGAGGCTGC | 146845 |
| rs138750666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588139 | GATGTTTACATCCTG[A/C]GTGACTCAGCAAGTT | 146845 |
| rs138755738 | snp | A/G | 0.000347185 | 0.0131709 | missense | CFAP52 | GRCh38.p7 | 17:9594200 | TTTGGCAGTGTGGTG[A/G]TGTGGAGCATAGCCA | 146845 |
| rs138772764 | in-del | -/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615622 | GTTACCCTTGAATTG[-/T]TTTTTTTTCTTTTAG | 146845 |
| rs138780836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600402 | GTGCCCCACCACACC[C/T]GACTAATTTTTGTAT | 146845 |
| rs138796102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615680 | GCTAGAGCACAGTGA[C/T]GCAATCACAGCTCAG | 146845 |
| rs138933683 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603307 | TCTGCCTCCAGAGTT[G/T]ACGCCATTCTCCTGA | 146845 |
| rs138938941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631307 | AAACACACTGGGCAT[A/G]GATAGAGCCTTTGCT | 146845 |
| rs139046989 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626288 | AGGCTGGAGTGTAAT[A/G]GCATGATCTCAGCTC | 146845 |
| rs139087892 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630052 | TCCTCACTGCCTCCC[C/T]TTTTTCTCTTATGCC | 146845 |
| rs139089477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9634751 | CCTGGGAGACGGACC[A/G]AGACTCCATCTCAAA | 146845 |
| rs139143365 | in-del | -/TCT | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622990 | TTAGTGTCATACAGA[-/TCT]TCTTCTCCTTATTGA | 146845 |
| rs139171654 | snp | C/T | 3.29522e-05 | 0.00405894 | CFAP52 | 17 | allele_origin=T(somatic)/C(germline) | 17:9612372 | AGGACACCAGTTTCT[C/T]GTAGGAACAGAAGAA | 146845 |
| rs139239296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609336 | AAAGTACATAGTATT[A/G]GAGGGTGATAAGTAC | 146845 |
| rs139321138 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613596 | GATTTCGACTCACTG[A/C]AACCTCTGCCTCCTC | 146845 |
| rs139528854 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B | CFAP52, USP43 | GRCh38.p7 | 17:9643421 | ATTAGAACTTTTAAC[A/T]TTTTGAATAAATTCT | 146845 |
| rs139631637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603648 | GTAGACAAACTGATT[C/T]TACAGTTTACACAGA | 146845 |
| rs139646371 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640517 | TTTCTGTTCCTGCGT[C/T]AGTTTGCTGAGGATA | 146845 |
| rs139646620 | snp | A/C/G | 0.0033974 | 0.0410755 | missense | CFAP52 | GRCh38.p7 | 17:9608153 | GCCTGAAGATGGGGG[A/C/G]TTTGTTGGTGGGCTC | 146845 |
| rs139653833 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | CFAP52 | GRCh38.p7 | 17:9632917 | AAAATCCGAGCCTTC[A/G]CCCCAGAGACAGGCC | 146845 |
| rs139671645 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601885 | GATGGTTCTAACTAA[C/G]CTTAGATACTTTTCC | 146845 |
| rs139764257 | snp | A/T | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637147 | TTGTTACAAATGTCG[A/T]TTTTGATTCATTAAA | 146845 |
| rs139797033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593030 | TATATGACTTCCTAC[C/T]TCCCTATTCCTGGTG | 146845 |
| rs139855675 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582249 | TTTCCAAAACGATTA[A/G]ACCGATTTACTCTCC | 146845 |
| rs139863455 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628974 | AGCCTCTCTTTGGAG[C/T]TTCCTTCCAGCTGGG | 146845 |
| rs139882429 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591976 | ATCCAAAATTCAAAA[G/T]CATGACTCTTATATC | 146845 |
| rs139936399 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9628918 | CATGTGGATAACCTA[A/G]AACAGCCTCCCACTG | 146845 |
| rs140009881 | snp | C/G/T | 4.99399e-05 | 0.00499679 | missense, upstream-variant-2KB, utr-variant-5-prime | CFAP52, STX8 | GRCh38.p7 | 17:9576715 | ATAACAAAATTTCGC[C/G/T]GGAGGCCCAAGTGGC | 146845 |
| rs140028264 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613162 | AACTTCTTTCCTGTC[A/C]TTTGTACCTCTTGAG | 146845 |
| rs140054356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588463 | GCCAGCTCAAGCAGC[A/G]GAGGCAGGGCAGACA | 146845 |
| rs140087416 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585711 | TGTGTTTTGTACTCA[A/G]GTAGAAAATTCCTGG | 146845 |
| rs140194948 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9579765 | TAGACACGGTGTTTC[A/G]CCACGTTGGCCAGGC | 146845 |
| rs140225455 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623086 | GAGTTCCACCTTTAT[G/T]TCTCACAGTTTTTGT | 146845 |
| rs140232866 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614772 | CTGGGCTCTACCCAT[C/G]AGACGCGAGTAGCAG | 146845 |
| rs140304927 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590037 | GCTGGGAGCTTTTCA[C/T]AGGCTTTGTCTGCCG | 146845 |
| rs140315215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629696 | GGGATTACAGGCACG[C/T]TCCTGCCTCAGCCTC | 146845 |
| rs140350447 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587269 | TTATCCAGTCTACCA[C/T]TGATGAGCATTTGGG | 146845 |
| rs140427266 | snp | A/C/G/T | 0.0477668 | 0.148125 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636916 | TGGGCGTGGTGGCGC[A/C/G/T]TGCCTGTTATCCCAG | 146845 |
| rs140498095 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603064 | CATGTAACACTACCT[G/T]AAAACTAGTGGATTT | 146845 |
| rs140517505 | snp | C/T | 0.00502848 | 0.0498894 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9635453 | AAGCTGGAGGAGGCC[C/T]TGAAGGAACACAAGT | 146845 |
| rs140629404 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638099 | TACGTCCAAACCTGT[C/G]TACAAATGTGTACAT | 146845 |
| rs140641061 | snp | C/G | 0.00057663 | 0.01697 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641761 | ATGGGACAGTAATCA[C/G]AGAATTGGAAGGTTC | 146845 |
| rs140676432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636412 | TCTTATGCTCCGAGC[A/G]TATCACACCCCCATA | 146845 |
| rs140749458 | in-del | -/TTTG | 0.4248 | 0.178731 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623671 | CTTTGCTTAGCTTTT[-/TTTG]TTTGTTTGTTTGTTT | 146845 |
| rs140750566 | in-del | -/T | 0.0442811 | 0.142055 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641702 | CTGAGTCCTGCTTAA[-/T]TGCTTCTTTCCTGAA | 146845 |
| rs140794884 | snp | C/T | 0.000109667 | 0.00740416 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584311 | CAGATATTTGGAGTA[C/T]GGGAGTTGCCTGTGG | 146845 |
| rs140835398 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593828 | GAATTACCCGGACAT[C/G]GTGGTGTGCGTCTGT | 146845 |
| rs140891449 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625331 | ATAACCAGAATTTAC[A/G]TCTTATTCTTGTGGT | 146845 |
| rs140905796 | snp | C/T | 4.95757e-05 | 0.00497849 | missense | CFAP52 | GRCh38.p7 | 17:9635556 | TCATTTGGGACCTTG[C/T]GTAGGTACCTGTGAT | 146845 |
| rs140921334 | snp | A/G | 6.61015e-05 | 0.0057486 | missense | CFAP52 | GRCh38.p7 | 17:9608176 | GTGGGCTCTGGAGCC[A/G]GACTGCTGGTCTTCT | 146845 |
| rs140931057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622265 | CAGAAAATATGGTCT[C/T]AGCCAGGTGCAGTGG | 146845 |
| rs140942649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599492 | CAGAGGATGCCTATT[A/G]ACATCAGAACCAGAT | 146845 |
| rs141029534 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624090 | TAATATGTCATTTTT[A/C]TGTTTATATTTCAAT | 146845 |
| rs141074400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638509 | GGCATGGAGATAAAC[C/T]AACCCAAATCCCAGC | 146845 |
| rs141182119 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603619 | TAAACATCCCAGCAA[C/G]TTATTTTGTGTCTGT | 146845 |
| rs141229371 | snp | A/C/G | 3.35268e-05 | 0.0040942 | missense | CFAP52 | GRCh38.p7 | 17:9628677 | TTCCTTGCAGTGGCA[A/C/G]TGCTGAGCTATTTGC | 146845 |
| rs141295874 | snp | A/C/T | 1.648e-05 | 0.0028705 | missense | CFAP52 | GRCh38.p7 | 17:9638644 | TGATACTAGCCAACA[A/C/T]CTTATTCCAGTGTGT | 146845 |
| rs141308784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608782 | AATGTGCTTATTCAG[C/T]ACCTCCTCCAACCAA | 146845 |
| rs141313059 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606025 | TGGGGAAATCTCAAA[C/T]ACTTGTATCTTCTGT | 146845 |
| rs141358587 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603248 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 146845 |
| rs141382632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624783 | TATAGAATATACTAT[A/G]GCAACTCTGTTCTCT | 146845 |
| rs141434430 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599122 | AGCCAGAAGTGTTTT[G/T]AATTTTGGATTTTCT | 146845 |
| rs141474394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594832 | TCTGCCTAAGGGAGG[A/G]AATAAATTAATTTAC | 146845 |
| rs141532385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596501 | TACAATTATTAATTC[A/G]GATTAATTCAACATA | 146845 |
| rs141641828 | snp | A/G | 0.039522 | 0.134904 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601024 | ACCCAAATGTCCAAC[A/G]ATGATAGACTGGATT | 146845 |
| rs141646758 | snp | A/G | 0.00113677 | 0.0238137 | missense | CFAP52 | GRCh38.p7 | 17:9628752 | ACAGGGAGCTGCTGC[A/G]GATCACCGTGCCCAA | 146845 |
| rs141662042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636764 | AAAAAACACAAAGCA[C/T]TGCTGGGCGCGGTGG | 146845 |
| rs141718755 | snp | A/G | 6.595e-05 | 0.00574201 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585940 | TCTGGAGAGTACATC[A/G]CCTCCGGACAAGTCA | 146845 |
| rs141765000 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576093 | TGGGAGCGCTGCAAG[A/T]CCTCTCTGTAGCAGT | 146845 |
| rs141768118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640293 | GCAGGTTTGTTCCAT[A/G]GGTAAACATGTGCCG | 146845 |
| rs141807222 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587613 | ACTTTGCATTTCTCT[A/T]ATGACCAGTGATATT | 146845 |
| rs141821696 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9621616 | ACCCAAATGTCCAAC[A/C]ATGATAGACTGGATT | 146845 |
| rs141890222 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578536 | AGAAAAAGAAAAACC[G/T]TGTGGCAGTGTATAG | 146845 |
| rs141891194 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580730 | GCAGTGATGGTTTTT[A/G]CTTCTCAAACTGGCA | 146845 |
| rs142148256 | in-del | -/A | 0.0711525 | 0.174681 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625213 | TCAATTAAAAAAAAA[-/A]CACAGTAGAATCCTC | 146845 |
| rs142157283 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598504 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT | 146845 |
| rs142250700 | snp | C/T | 1.65507e-05 | 0.00287664 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643060 | AGTTTGGGATTATAA[C/T]GAGGGTGAAGTGACT | 146845 |
| rs142265555 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602546 | GGACATTTGGGTTGG[C/T]TCCAAGTCTTTGCTA | 146845 |
| rs142270982 | in-del | -/AA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580689 | GTGAGACCTGGTCTC[-/AA]AAAAAAAAAAAAAAT | 146845 |
| rs142273503 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632670 | GGAATTGAGGGTAAT[C/T]AAGGAAGACTCAGGC | 146845 |
| rs142289033 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | CFAP52 | GRCh38.p7 | 17:9635526 | GTGTCACCGCCAGCA[C/T]CGATGGGACTTGTAT | 146845 |
| rs142293963 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631416 | ATCTTTGCTGAAATG[A/G]GATCTACCTTTAGCA | 146845 |
| rs142316723 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637949 | CCAGCTCCCTCTTGG[G/T]GGCACCCTGGGCAGG | 146845 |
| rs142381148 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9605529 | CCATCCTGGCCATCT[C/T]TACTAAAAATACAAA | 146845 |
| rs142381438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595353 | ATTGTTTCCTGTCCC[C/T]GCTTTATGATATGCA | 146845 |
| rs142418111 | snp | A/G | 4.94181e-05 | 0.00497057 | missense | CFAP52 | GRCh38.p7 | 17:9600154 | AAACTGCTGACAGAT[A/G]TTGGGCCTGCGAAGG | 146845 |
| rs142481098 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589137 | CAAAATATATTAGGA[A/G]GAACAATCAATGCAA | 146845 |
| rs142496927 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631060 | AGAGAGAGAGAAAGA[A/G]AGAAAGAAAGAAAGA | 146845 |
| rs142505032 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631058 | AGAGAGAGAGAGAAA[A/G]AAAGAAAGAAAGAAA | 146845 |
| rs142636794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613869 | TCCGTTCCCTGAATC[C/T]CTGTGATTAGGTCTT | 146845 |
| rs142701617 | in-del | -/AAAAAAA/AAAAAAAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9598761 | GTGACACTCTGTTTC[-/AAAAAAA/AAAAAAAA]AAAAAAAAAAGAAGA | 146845 |
| rs142708763 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607434 | GTGGATACTATAAAA[C/T]AACCATCATACATTG | 146845 |
| rs142708928 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613061 | TATTAAGTGCATTTT[C/T]GACTTAGGATATTTT | 146845 |
| rs142776056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9639650 | GAATAACAAGTGAAC[A/T]AGAGATGAGATGGTG | 146845 |
| rs142829796 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-5-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643502 | ACAGACCTTCCTCAT[A/G]ATCTGTGCACAGACA | 146845 |
| rs142850889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581246 | GGCGTGAACCCGGAA[A/G]TGCTGGTTGCACAGC | 146845 |
| rs142953577 | in-del | -/T | 0.416382 | 0.186593 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629496 | TTCTTTCTTTCTTTC[-/T]TTTCTTTTCTTTCTT | 146845 |
| rs143000931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626087 | GCTTGGTACCTCATC[A/G]TGATCCAATCAATTG | 146845 |
| rs143011898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600713 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAGC | 146845 |
| rs143018725 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590755 | GTAATTTTAAGCTGC[C/T]TAAAATTTGTTTGCA | 146845 |
| rs143049274 | snp | A/G | 0.00317525 | 0.0397183 | synonymous-codon, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641789 | TTCCCTGTCTGGGTC[A/G]ATAAATGGCATGGAT | 146845 |
| rs143061433 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588167 | GTTTAGAGTGCAGGC[A/G]TATAATTCCACTGTT | 146845 |
| rs143104021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636567 | TTAGAATCGGATGCC[A/G]TTCCTCCACCCCTCT | 146845 |
| rs143153799 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628204 | AGGGCATTAAATACC[A/G]TTTACACAAGATGTT | 146845 |
| rs143187282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590434 | CCTTCTTTTTGCCAC[A/G]GCAGAGGGCACTAGA | 146845 |
| rs143190154 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625529 | CCACTAGGATATTCC[A/C]CCTTTAAATTCCAGC | 146845 |
| rs143445180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636685 | GGGAGGAAGGAGGCA[C/T]GCACGACAAAGAACA | 146845 |
| rs143482450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583570 | GCATAAAAGGAGACT[C/T]ATGAAGAAACATATC | 146845 |
| rs143501761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623983 | TTACAGAATTCTTGC[C/T]CGATTATTTTCTATT | 146845 |
| rs143563239 | snp | A/G | 0.000684158 | 0.0184827 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576788 | CTCCAGCATCTTTGG[A/G]CTGGCTGGTTTAGGA | 146845 |
| rs143568386 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608416 | GCTTATGTTGAATCA[A/G]ACCAAAGTAGTCCAC | 146845 |
| rs143579503 | snp | C/T | 0.00480031 | 0.0487557 | intron-variant, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585915 | CGTCTCCTGCTTGGC[C/T]ATCTCCAGGTCTGGA | 146845 |
| rs143603836 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9603678 | AGGGGCAAAAGACTC[C/T]GACTAGAAAGCACAA | 146845 |
| rs143647886 | in-del | -/AGAA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597860 | GAGAGAAAGAGAGAG[-/AGAA]AGAAAGAAAGAAAGA | 146845 |
| rs143697444 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610230 | TATGTTGGGTTATCT[C/G/T]TGGATGTATGAAGTG | 146845 |
| rs143961097 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598053 | CTAATTTGGGAGGGG[A/G]GATCATAAAACCTGC | 146845 |
| rs143968723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588929 | CCAACCTAGTGAAAC[A/G]CTGTCTCTACTAAAA | 146845 |
| rs143991289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635325 | CAAGCATAGCAAAGG[A/G]GAAAAAGCTCTTGGA | 146845 |
| rs144038113 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608601 | ATTATGCAATGGGTA[A/C]CTATTATGTGCAAAG | 146845 |
| rs144191245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609461 | GCTCTTTGGGAGGTC[A/G]AGGCAAGTGGATCGC | 146845 |
| rs144257813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605439 | AGATCAGGCTGGGCG[C/T]GGTGGCTGACACCAC | 146845 |
| rs144300561 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640726 | GCAACCTCCTACAAC[G/T]TTCACCTCCTGGGTA | 146845 |
| rs144319003 | snp | C/T | 0.000381651 | 0.0138087 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9633018 | AAGGGTCATCAGTGG[C/T]GGTGGGGAAGGGGAG | 146845 |
| rs144371237 | snp | A/G | 1.64982e-05 | 0.00287208 | missense | CFAP52 | GRCh38.p7 | 17:9594314 | GAGATGTTTATGACT[A/G]CTGGAAAGTATGTGT | 146845 |
| rs144391287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638187 | AACAAAATAAAATAC[C/T]CTTCCCCACATTCTG | 146845 |
| rs144401450 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628514 | CAAACTCCTGACCTC[A/G/T]TGATCCACCCCCCTG | 146845 |
| rs144465881 | snp | C/T | 0.000214502 | 0.010354 | missense | CFAP52 | GRCh38.p7 | 17:9638610 | AATCTACTTTCCAGG[C/T]GTCTCAGGAGGAATC | 146845 |
| rs144485665 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635699 | TGTTCATCAGAAGCC[A/G]TTCATGACGGTCCAT | 146845 |
| rs144543717 | snp | C/G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575561 | ATATTCAGAGATTTG[C/G/T]CGTAAGTCCTCAGCT | 146845 |
| rs144564279 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612722 | ACCCCTCATGGAAAG[A/G]GTAAGTACCTGACAA | 146845 |
| rs144675275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586973 | TTTCATCAACCAGGT[A/G]CTCAGCCTAGTACCC | 146845 |
| rs144696580 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615990 | ATAGTTTTTCGGGGG[C/G]AGGAGCCAAGATGGC | 146845 |
| rs144765305 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584690 | GCAATAGTGTGATCT[C/T]GGCTCACTGCAACCT | 146845 |
| rs144808343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624202 | AAACTTTTTGAATCT[A/G]TAAGCTGATATTTTC | 146845 |
| rs144847536 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592625 | CATACAATATGTGGT[A/C]TTTTGTGACTGGCTT | 146845 |
| rs144892229 | snp | A/G | 0.00677283 | 0.0577974 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622552 | TTTCTATTAAAAAAA[A/G]AAGAAGAAGAAGAAG | 146845 |
| rs144929134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613889 | GATTAGGTCTTTCCA[C/T]GTTATTTCTAACAGT | 146845 |
| rs145032534 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590154 | GTGATCAATCTTCTT[C/T]GATCCATGGTATCTT | 146845 |
| rs145070409 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629726 | CCCAAGTATCTGGGA[C/T]TACAGGCGTGTGTCA | 146845 |
| rs145103496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606793 | GTCTCCTCATAGGCT[A/G]AGCCTTCATCCTGTT | 146845 |
| rs145130650 | snp | C/T | 0.000132749 | 0.00814598 | missense | CFAP52 | GRCh38.p7 | 17:9608200 | GTCTTCTGTAAAAGC[C/T]CTGGCTACAAACCCA | 146845 |
| rs145147887 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603295 | CTCACTGCAAGCTCT[A/G]CCTCCAGAGTTTACG | 146845 |
| rs145149414 | in-del | -/CA | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9585670 | AGTGCAAGACTCTGT[-/CA]CACACACACACACAC | 146845 |
| rs145153199 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637424 | CACGTTTGAAAACTT[A/C]CATAATGAGAAGAAA | 146845 |
| rs145177791 | in-del | -/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592928 | TAGTTATCATTTAAA[-/C]TTTTTAAGTAGTTTA | 146845 |
| rs145237801 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633544 | TGTACACAGAAAGGA[C/T]GTTTACAATACAGAC | 146845 |
| rs145277034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602202 | TACATAGGTATACAC[A/G]TGCCATGGTGGTTTG | 146845 |
| rs145293486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577746 | ATTGAGCAGCCTACA[A/G]TGGGTTGCATAATGT | 146845 |
| rs145298736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599238 | TTCCTTGGAGTGTCA[C/T]ATCAGCACTCAACAA | 146845 |
| rs145370335 | in-del | -/C/TC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9615819 | TTTTTTTTTTTTTTT[-/C/TC]CCCAGAAACAGGGTC | 146845 |
| rs145373923 | snp | C/G | 0 | 0 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613829 | CGGCCTCAGACCTCA[C/G]TTTTTGAGATCTTGA | 146845 |
| rs145482024 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623445 | ATCTTTCATATGTTT[G/T]TATTAAATCTTTATA | 146845 |
| rs145531628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587413 | CTGGGTTGAATGACA[A/G]TTCTGTTTTTAGCTG | 146845 |
| rs145618994 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586057 | CAAGTTGTTAGTTCT[A/G]TGTGGCAATGTGCTT | 146845 |
| rs145626755 | in-del | -/AAGT | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575925 | AGCCTGGAGTTTGCA[-/AAGT]TGAGTAGCTAGGGCC | 146845 |
| rs145662842 | snp | A/G | 0.000477614 | 0.015446 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585811 | TGCCATCCTGACCAG[A/G]AGCATATGATTTATC | 146845 |
| rs145751336 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578615 | TAATGGCACAATCTC[G/T]GCTCACTGCAACCTC | 146845 |
| rs145792282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610355 | CAGGTTTGTGCTATC[A/G]CTGTTTCCAAAATAA | 146845 |
| rs145827979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636430 | TCACACCCCCATAGA[A/G]TGACTAACTTCAAAC | 146845 |
| rs145922964 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631572 | GGAGATCGCTTGGTG[A/G]ATTTGAGGAATAGCA | 146845 |
| rs145951373 | snp | C/T | 0.00133431 | 0.0257949 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9628801 | CGACTTCATGAGGGA[C/T]GGCAAAAGCATCATT | 146845 |
| rs146008600 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580582 | TAGTCCCAGCTATTC[A/G]AGAGGCTGAGGTGGG | 146845 |
| rs146045510 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613110 | CAGGCATATAGCCCC[A/G]TCTTAAGACACGAAG | 146845 |
| rs146057434 | snp | A/G | 0.00100459 | 0.0223894 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612390 | AGGAACAGAAGAATC[A/G]CACATTTATCGTGTC | 146845 |
| rs146156224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600877 | GGCCAGTTCTCTATG[A/C]CCTCGTCTCTGGTTT | 146845 |
| rs146193554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593228 | CATTTTTTTGTATTA[C/T]GATCCACACCCTATT | 146845 |
| rs146275247 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584866 | GACCTCAGGTGATCC[A/G]CCTGCCTCGGCCTCC | 146845 |
| rs146289590 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643333 | TTCTCTTTTTCTTTA[G/T]AGAATGCATTTTATA | 146845 |
| rs146367373 | snp | C/T | 0.000461673 | 0.0151863 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632916 | TAAAATCCGAGCCTT[C/T]GCCCCAGAGACAGGC | 146845 |
| rs146475642 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624067 | TATTCTTATGATTTT[C/G]TTCTTTATAATATGT | 146845 |
| rs146525637 | snp | A/C | | | missense | CFAP52 | GRCh38.p7 | 17:9594240 | CCATCTGTGGCAGCC[A/C]TGCAGCCGGCCTCAA | 146845 |
| rs146544451 | snp | A/G | 1.64738e-05 | 0.00286995 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585858 | CCTCATTCAGGCAAT[A/G]AATACTAAAGAGCAG | 146845 |
| rs146548028 | snp | C/T | 0.000611242 | 0.0174713 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608175 | GGTGGGCTCTGGAGC[C/T]GGACTGCTGGTCTTC | 146845 |
| rs146584137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605892 | GGAACCCTAATGTAC[A/G]CAATGGATTTTGGGT | 146845 |
| rs146594945 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603247 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 146845 |
| rs146620915 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638404 | CACTGATAGGCCAAC[C/T]GGAGTACACAGAAGT | 146845 |
| rs146702172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589978 | GCTCTTCACAGTGCT[C/T]GTGTGTTTCCTTGGT | 146845 |
| rs146740011 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626907 | ACTCTTTTTTGAAAT[G/T]TGTTCATGAAAAAAT | 146845 |
| rs146796396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577168 | GGATGCTGTCTGTGT[A/C]GGCCCCTGGGACCAG | 146845 |
| rs146809968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638063 | CAGGCTCGTGCTTTC[C/T]GAGGGTTGTGCATGA | 146845 |
| rs146836355 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636336 | ACTTCCCATGGAGGG[A/G]AGGGATGCTGGTGGG | 146845 |
| rs146845939 | snp | C/T | 0.000609319 | 0.0174439 | missense | CFAP52 | GRCh38.p7 | 17:9600164 | CAGATGTTGGGCCTG[C/T]GAAGGACAAATTCAG | 146845 |
| rs146928155 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611259 | ACTTTTTTTTTTTAA[A/G]TTCATACTCATTATA | 146845 |
| rs146937773 | snp | A/G | 1.65767e-05 | 0.00287891 | missense | CFAP52 | GRCh38.p7 | 17:9608128 | CCCTAGGGAGTGTCA[A/G]CTATCAGGTGCCTGA | 146845 |
| rs146979019 | snp | A/G | 0.000510755 | 0.0159724 | missense | CFAP52 | GRCh38.p7 | 17:9638665 | TCCAGTGTGTGTGCT[A/G]TCACCCTGAGGAGTT | 146845 |
| rs147033633 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595162 | GGGAAGGTTAAATAT[G/T]AATTTTAGAAATCCT | 146845 |
| rs147201188 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603730 | ACGGGTAATATAGAT[A/G]ATGTAGATGACGGGT | 146845 |
| rs147276801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625219 | AAAAAAAAAACACAG[C/T]AGAATCCTCCCTGGT | 146845 |
| rs147286982 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622210 | ATCAATCCCCTTAGA[C/T]TCTTTTTGTTTTGGA | 146845 |
| rs147354190 | snp | C/T | 4.94303e-05 | 0.00497119 | missense | CFAP52 | GRCh38.p7 | 17:9594267 | TCAATGTTGGCAATG[C/T]CACCAATGTGATCTT | 146845 |
| rs147381890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603633 | AGTTATTTTGTGTCT[A/G]TAGACAAACTGATTC | 146845 |
| rs147392419 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601792 | CAGTAACTTATCAGG[C/G]CTGTTTCTACTAAAC | 146845 |
| rs147486114 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588370 | CAGCTCAGCCCGCTC[A/G]TGCCCAGAGAGACAA | 146845 |
| rs147509941 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628306 | TTTTTTTGAGATGGA[G/T]CCTAGCTCTGTCACC | 146845 |
| rs147551886 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614403 | TCAGGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 146845 |
| rs147629560 | in-del | -/AG | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9631081 | GAAAGAAAGAAAGAA[-/AG]AGAAAGAAAGAAAGA | 146845 |
| rs147646589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602218 | TGCCATGGTGGTTTG[C/T]TGCACCCATTAACCC | 146845 |
| rs147656194 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599278 | TTGGAGCATTTCAGA[G/T]TTTAGATTTTTAGAT | 146845 |
| rs147829154 | snp | A/C | 4.94401e-05 | 0.00497168 | missense | CFAP52 | GRCh38.p7 | 17:9638642 | GATGATACTAGCCAA[A/C]ACCTTATTCCAGTGT | 146845 |
| rs147844022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635883 | GGCAAGAAAAATAAC[A/G]AATGCAAGGTCGGGC | 146845 |
| rs147867103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633229 | TTATTTTGAAATGGA[A/G]TCTCACTCTGTCACC | 146845 |
| rs147939471 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582394 | CATAATTTACATTTT[C/G]CTGGTTACTTATGAG | 146845 |
| rs147982997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636706 | ACAAAGAACATGAGA[C/T]ACGCTTGATGGGAAT | 146845 |
| rs148001781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583872 | AAGTTTGGGCCACTT[A/G]TCACTTGAAAGCTAA | 146845 |
| rs148055444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587523 | TCTTTGCAACCTCAC[C/T]AGCATCTGTTATTTT | 146845 |
| rs148194324 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603575 | ATGAGTTCTTCTTAA[C/T]TTGAACTATAGATTT | 146845 |
| rs148229360 | in-del | -/AT | 0.0441095 | 0.141807 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584048 | GCATTTTTGTGAAAC[-/AT]GTGCAGTCTCAGGTA | 146845 |
| rs148248120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608639 | TTAATCATGCATTTG[A/T]ATACAATTTATAATA | 146845 |
| rs148288821 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590751 | TGCTGTAATTTTAAG[A/C]TGCCTAAAATTTGTT | 146845 |
| rs148341486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596342 | CTGAGCTCAGGCAAT[C/T]CACCTGCCTCGGCCT | 146845 |
| rs148468122 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576075 | AGCATTTTCCCAGGA[A/G]GGTGGGAGCGCTGCA | 146845 |
| rs148508276 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581234 | AGGCAGGAGAATGGC[A/G]TGAACCCGGAAGTGC | 146845 |
| rs148510531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605428 | AGACAATAAAAAGAT[A/C]AGGCTGGGCGCGGTG | 146845 |
| rs148584020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626015 | TCTATAGCTACATCT[A/G]TATCTATAAATATCT | 146845 |
| rs148590702 | in-del | -/AA | 0.0115144 | 0.0749975 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589733 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 146845 |
| rs148657355 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598127 | TGCACTAGGCCATAA[C/T]GAAGCCTCAAAAATG | 146845 |
| rs148721106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637923 | GCCGGGCTCTCTTCA[G/T]TTGCGGGAGGCCAGC | 146845 |
| rs148740350 | snp | A/C | 0.0115307 | 0.0752106 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585443 | GGAGGCTAAGGTGGA[A/C]GGATCACGAGGTCAG | 146845 |
| rs148792833 | snp | A/G | 1.67674e-05 | 0.00289541 | missense | CFAP52 | GRCh38.p7 | 17:9598268 | GAATTGGATCTTCCA[A/G]ATAGAAAAATCTGGC | 146845 |
| rs148794571 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9589056 | GCAGTGAGCGAAGAT[C/T]GCACCACTGCACTCC | 146845 |
| rs148803926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628565 | TACAGGTTTGAGCCA[C/T]CGCGCCCAGCCTTTT | 146845 |
| rs148827882 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582871 | CAAACTCCCAGCCTC[A/G]AGTGATCTGCCTGCC | 146845 |
| rs148837689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623512 | TTTTTGCTTTAAAGA[A/G]TCATAAACATTTTCA | 146845 |
| rs148905544 | snp | A/C/T | 0.000971656 | 0.022022 | intron-variant, missense, synonymous-codon | CFAP52 | GRCh38.p7 | 17:9585891 | CTTCCTACAGGGTCA[A/C/T]GGCAACAACGTCTCC | 146845 |
| rs149016984 | snp | C/T | 0.463451 | 0.130149 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615819 | TTTTTTTTTTTTTTT[C/T]CCCAGAAACAGGGTC | 146845 |
| rs149106566 | snp | A/G | 0.000131798 | 0.00811675 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9612381 | GTTTCTCGTAGGAAC[A/G]GAAGAATCGCACATT | 146845 |
| rs149175006 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595100 | TTCACCACATTGGCC[-/G]GGTTGGTCTCCAACT | 146845 |
| rs149175633 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633642 | CTTGCTCTTTTCCTC[C/T]GAGGATCGTGGTTGT | 146845 |
| rs149194646 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577894 | GTCAGGAGTTCGAGA[C/T]CATCCTGTCCAACAT | 146845 |
| rs149196269 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640930 | ATTATAGGTGTGAGC[C/T]GCTGCACCCAGCTGG | 146845 |
| rs149280526 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9574929 | GTTCTTGGAATCCAT[C/T]CTTCTAATATCCAGG | 146845 |
| rs149304215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612601 | TCCTTAAATTTTTCT[A/G]ACGTGGTGAATTATT | 146845 |
| rs149344663 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615923 | GGCCTCTCAGATTAT[A/G]GGCATGAGCCACTGC | 146845 |
| rs149419257 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592464 | ACAAGAGCAAAACTC[C/T]GTCTCAAAAAAATTA | 146845 |
| rs149428354 | snp | C/T | 0.00817763 | 0.0634188 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9632898 | GCCAGCATGGAACGA[C/T]GGTAAAATCCGAGCC | 146845 |
| rs149504656 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642743 | ATATATGATGTATAT[A/G]TATACCAGTATACTT | 146845 |
| rs149515574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580274 | TAGTCTCAAGAGACC[A/G]TATTGCCCACAAAGC | 146845 |
| rs149568809 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585311 | TGATTACTAGATGAA[C/T]GTTTTTGTCAGTGAA | 146845 |
| rs149630996 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9628383 | CTTCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 146845 |
| rs149663084 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623432 | TACATTTAATATAAT[C/G]TTTCATATGTTTGTA | 146845 |
| rs149758398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605210 | ATGTCCTTCAGTAAG[C/T]AAAGGGATACGTAAA | 146845 |
| rs149768145 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640553 | TCCCAACTCCATCCA[G/T]GTCCCGGCAAAGGAC | 146845 |
| rs149819920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582270 | TTTACTCTCCCACCA[A/G]GCATTTTATGAGTGT | 146845 |
| rs149874076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586257 | TTGTAGAACCTGATC[C/T]GATTTCTAGAAAAGT | 146845 |
| rs149894242 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597869 | AGAGAGAGAAAGAAA[G/T]AAAGAAAGAAAAGAA | 146845 |
| rs149896840 | snp | A/G | 0.14665 | 0.227637 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626375 | GCTGGGACTACAGGC[A/G]CACACCACCACACCC | 146845 |
| rs149950268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629718 | CTCAGCCTCCCAAGT[A/G]TCTGGGACTACAGGC | 146845 |
| rs149961740 | snp | A/G | 0.000132247 | 0.00813055 | synonymous-codon | CFAP52 | GRCh38.p7 | 17:9608181 | CTCTGGAGCCGGACT[A/G]CTGGTCTTCTGTAAA | 146845 |
| rs149990362 | in-del | -/T | 0.0399052 | 0.1355 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592698 | ATGCACAGTATTTCA[-/T]TTTTTTATCATCAAA | 146845 |
| rs150116794 | snp | C/G | 0.000399281 | 0.0141238 | missense | CFAP52 | GRCh38.p7 | 17:9612457 | TGTCACTTTGATGCT[C/G]TCGAGGATATTGTCT | 146845 |
| rs150136894 | snp | A/G | 0.000758325 | 0.0194573 | intron-variant, missense | CFAP52 | GRCh38.p7 | 17:9585946 | GAGTACATCGCCTCC[A/G]GACAAGTCACATTCA | 146845 |
| rs150190874 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587809 | TATTTTCTGCAAGGC[A/G]TATTTCCAGAAGTGA | 146845 |
| rs150324599 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579815 | TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 146845 |
| rs150347945 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614989 | AGAGTTTATTAAATT[A/C]CTAATAAGAAAGAAA | 146845 |
| rs150401477 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624842 | AAATTTTGCCTCCCC[A/G]TAGTATGCATCATCT | 146845 |
| rs150409434 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9633361 | AGGCGCACACCGTCA[C/T]GCCCAGCTAATTTTT | 146845 |
| rs150503527 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | CFAP52 | GRCh38.p7 | 17:9628760 | CTGCTGCGGATCACC[A/G]TGCCCAACATGACCT | 146845 |
| rs150541280 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636901 | AATACAAAAAGTAGC[C/T]GGGCGTGGTGGCGCG | 146845 |
| rs150592698 | snp | C/G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9576596 | GCTGGGTTTCTGCGC[C/G/T]GGCGTGGAGCTGGAG | 146845 |
| rs150594521 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640308 | AGGTAAACATGTGCC[A/G]TGGTGGTTTGCTGTA | 146845 |
| rs150616545 | in-del | -/AT | 0.0252325 | 0.109451 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635682 | CAACACAGTAAAGGG[-/AT]ATGTTCATCAGAAGC | 146845 |
| rs150645595 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581669 | TTGTAGTGGACATGC[A/G]TAGTTTTGGTTACTC | 146845 |
| rs150666055 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591960 | CCTACTATGCAAAAG[G/T]ATCCAAAATTCAAAA | 146845 |
| rs150675216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631182 | TGACAAAGATCCCCC[C/T]ATCACCTACAAGGCT | 146845 |
| rs150719465 | in-del | -/A | 0.304438 | 0.244001 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590828 | AAACCTTGCTGTACT[-/A]AAAAAAATGCAATAT | 146845 |
| rs150802282 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609179 | TGTGTTGAACATTCA[C/T]GGGGTACCAGGCATC | 146845 |
| rs150857037 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613494 | TTTGTTTTTTGTTTT[G/T]GGGGGGTTTTTGTTT | 146845 |
| rs150886022 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596856 | GACTAGCTGGGATTA[C/G]AGGTGCCCACCACCA | 146845 |
| rs150918260 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589452 | ATAATAAATGTATTG[A/G]CCGGGTGTGGCAGCT | 146845 |
| rs150971794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593808 | TGTCTCTACTAAAAA[C/T]ACAAGAATTACCCGG | 146845 |
| rs151109931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611184 | GCGTTGAATTCTTCA[C/T]TGTCTAAACTAAACT | 146845 |
| rs151124246 | in-del | -/T | 0.0422008 | 0.138995 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608002 | CATTAATATTTAAAA[-/T]TTTTTTTATTGCCAT | 146845 |
| rs151131928 | snp | C/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9626158 | AACAATCTACCACTT[C/G]AATGGTTCAGTTTTG | 146845 |
| rs151185341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629454 | CCAGGAAACCATCTC[A/G]CCCCTCTTTTCTTTC | 146845 |
| rs151198307 | in-del | -/A | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9640062 | ATTACAAAGCAAAAG[-/A]AAAAAATTAACAAGA | 146845 |
| rs151243943 | in-del | -/TCAAATATAC | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9584590 | TAAGATCAACTCTTT[-/TCAAATATAC]TAGCAGATTAATGCA | 146845 |
| rs151248064 | snp | A/G | 0.000131833 | 0.00811782 | missense | CFAP52 | GRCh38.p7 | 17:9635528 | GTCACCGCCAGCACC[A/G]ATGGGACTTGTATCA | 146845 |
| rs151259266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602900 | CATATGTTTGTTGGC[C/T]GCATAAATATCTTCT | 146845 |
| rs151321583 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CFAP52 | GRCh38.p7 | 17:9641333 | CTAGAACTCTGGGGA[C/G]TGGGGAGTGCTCATC | 146845 |
| rs180713526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627475 | GACCATTGCACTCCA[A/G]CCCAGGCAACAGAGT | 146845 |
| rs180734689 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579586 | TTGAATTTTGTTTTT[C/G]AGATGGAGTCTCACC | 146845 |
| rs180742518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602685 | AGATCCTTGAGGAAT[C/T]ACCACACTGTCTTCC | 146845 |
| rs180749846 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585594 | GAGAATCACTTGAAC[C/T]CAGGAGGTGAAGGTT | 146845 |
| rs180803865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9636779 | CTGCTGGGCGCGGTG[A/G]CTCCCGCCTGTAACC | 146845 |
| rs180813214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593103 | TCCATATGTAGAAAA[C/G]TTGGGAAATATAGTT | 146845 |
| rs180836141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612924 | ATTACATGAGATATT[C/T]GACACTTTATTATAA | 146845 |
| rs180974013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9582376 | ATGGTATCTCATTTC[A/G]GACATAATTTACATT | 146845 |
| rs181005315 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9631195 | CCCATCACCTACAAG[G/T]CTCCATGTGAATTTC | 146845 |
| rs181005737 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9609001 | AGAGGATGACCTTCT[C/T]GGGATGGAAAGATCA | 146845 |
| rs181015124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588839 | GTAATGGCACAATCT[C/T]GGCTCACTGCAATCT | 146845 |
| rs181066084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640884 | CCTGACCTCAAGCAA[C/T]GGGCCCAACTCGGCT | 146845 |
| rs181071995 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622306 | TAATCACAGCACTTT[A/G]GGAGACTGAGGTGGG | 146845 |
| rs181085085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597884 | GAAAGAAAGAAAAGA[A/C]AAAGAGGAAGACATT | 146845 |
| rs181205572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9635821 | CCACACAGTGAAGCA[C/T]GGTTTAACTTACACG | 146845 |
| rs181222295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612648 | TGTCTTTGCCATGCA[A/G]TTATATTAGCTTTCC | 146845 |
| rs181227201 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9592803 | TTCTAAATTATTATT[A/G]ATAATGGCGCTATGA | 146845 |
| rs181233418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9579207 | AAAACTATACTAGCT[C/T]TAAAAAAAAGAGGGA | 146845 |
| rs181428110 | snp | C/G | | | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575049 | TTTTTAATTATTAAG[C/G]AGAAAGGTCAAGTCT | 146845 |
| rs181432818 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9597252 | ATTTCTTCCCATTGC[A/G]TACATATACCACATT | 146845 |
| rs181438972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581703 | TCTGAATACTATTCT[A/G]TTTGAGAAGTATCCC | 146845 |
| rs181520052 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588429 | GGTAGAGCTGGCTGC[A/G]CAGCTGTATGTGGGA | 146845 |
| rs181635497 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9578422 | ATTGTTCTTATGGCG[A/G]GTTGAACAGGGCTTC | 146845 |
| rs181649965 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9608898 | TAAGGTATGTACACA[C/T]GAAAGAAGTCACTAC | 146845 |
| rs181743544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627560 | ACTTCACAGGAAAGG[A/G]TTTGTTTATTCTCTC | 146845 |
| rs181746335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9603309 | TGCCTCCAGAGTTTA[C/T]GCCATTCTCCTGACT | 146845 |
| rs181825457 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612012 | GTGGTCATTTGTACC[C/T]ATATGCCTGCCTGGA | 146845 |
| rs181931842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9622798 | ACCCTGGTAAAGCAA[C/T]AGAACATTTTTATCA | 146845 |
| rs181935310 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9598683 | GGAGAATTGCTTGAA[C/G]CTGGGAGGCGGAAGT | 146845 |
| rs181936649 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630651 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACCTCG | 146845 |
| rs181941953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583044 | CTTACTTTTGTACAC[A/G]CTGTCTTGTTTTTCA | 146845 |
| rs182004032 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9617148 | CCAATACAGAGAAGT[A/G]CTTAAAGGAGCTGAT | 146845 |
| rs182083236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592076 | CATAAAATTGACCCG[C/T]GTTAAGGTGTACAGT | 146845 |
| rs182128949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629249 | ATAAATTATAGGCAG[C/T]GTGATATTCCACCTC | 146845 |
| rs182141453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9605011 | AATGCAAAATAGTAC[A/G]GCCACTTTGGAAGAT | 146845 |
| rs182160437 | snp | A/C/G/T | 0.00160474 | 0.0282814 | intron-variant | CFAP52 | GRCh38.p7 | 17:9608229 | CATCAAGTAAGTTCC[A/C/G/T]GGTCTCACACAGTGG | 146845 |
| rs182185292 | snp | G/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9634774 | ATCTCAAAAAATGAA[G/T]GAATACCATACTAAC | 146845 |
| rs182215122 | snp | C/G | 0.000798403 | 0.0199641 | missense, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9641749 | GGGAAGTATTTGATG[C/G]GACAGTAATCAGAGA | 146845 |
| rs182354781 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575505 | AACCAGGATGGGCGG[C/G]AAATCCCCGCAACGA | 146845 |
| rs182432911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588166 | AGTTTAGAGTGCAGG[C/T]GTATAATTCCACTGT | 146845 |
| rs182560715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638768 | AGAAAAGCAGTGAGG[C/T]GTTGTGGTGGAGGGT | 146845 |
| rs182735297 | snp | A/G | 0.00443727 | 0.0468968 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584375 | TCAGAGCACCTGGTG[A/G]GCACTCAGAACTGAA | 146845 |
| rs182738925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9638277 | TGTGGGAGGCAGCAG[G/T]TTGGCTGTGAGTTCA | 146845 |
| rs182744395 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9613747 | TGGTCTTGAACTCCC[A/G]ACTTCAAGTGATCCA | 146845 |
| rs182755035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9594621 | AAACAATTTGCACAA[A/T]TGCACAGATTCACCT | 146845 |
| rs182762206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9580500 | TGAGACCAGCCTGGG[A/C]AACATGGTGAAACCC | 146845 |
| rs182816009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9624801 | AACTCTGTTCTCTGA[G/T]GATTGTTGGCATGGA | 146845 |
| rs182963599 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9590084 | TTCCGTGAGAATCCA[A/G]TTGTTTTTTGAATAC | 146845 |
| rs182967629 | snp | G/T | | | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642232 | CCCACCAAAACAAAT[G/T]AATTAACCAATATTT | 146845 |
| rs182969819 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9623515 | TTGCTTTAAAGAGTC[A/G]TAAACATTTTCAAGA | 146845 |
| rs182973731 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577631 | GGACTTAGCTCTTGA[C/T]TCTTGGTTTAACTTT | 146845 |
| rs182977985 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9599954 | CCATGTTGGTCAGTC[C/T]GGTCTTGAACTCCTG | 146845 |
| rs183003068 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CFAP52 | GRCh38.p7 | 17:9604593 | GCCAACATGGTGAAA[C/T]CCCGTCTCTACTAAA | 146845 |
| rs183007873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CFAP52 | GRCh38.p7 | 17:9600666 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 146845 |
| rs183090750 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629352 | AATCTATCTGTAAGT[A/C/G]TCCCCAGTGCTCAGA | 146845 |
| rs183112021 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9642633 | TCAATAAATAAATAA[A/G]TAAAAAATAAATAAA | 146845 |
| rs183184917 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CFAP52 | GRCh38.p7 | 17:9593897 | TTGAATCCAGGAGGC[A/G]GAGGTTGCAATGAGC | 146845 |
| rs183190938 | snp | C/T | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9580146 | ACTATAGCCCATGGG[C/T]CAAATCTGGCCCACT | 146845 |
| rs183288912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9586174 | ACCCGAGGTTGCAGC[C/T]TGTGACTGATAATGC | 146845 |
| rs183346358 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CFAP52 | GRCh38.p7 | 17:9625656 | GTTGGAGGCTCCCAC[A/T]TGTGAGAAAGCCACA | 146845 |
| rs183348498 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CFAP52 | GRCh38.p7 | 17:9601426 | TAATAATAAAATTTT[A/T]AAAAAAGTACCACAT | 146845 |
| rs183355845 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9584902 | GCTGGGATTACAAGG[A/G]TGAGCAACCGTGCCT | 146845 |
| rs183367987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627963 | TGAACTCCTGGCCTC[A/G]AGTCATGGGATCCTC | 146845 |
| rs183581080 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CFAP52 | GRCh38.p7 | 17:9610623 | CACTGCAACCTCCGC[C/G]TCCCGGGTTCAAGAG | 146845 |
| rs183591899 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587522 | TTCTTTGCAACCTCA[A/C]CAGCATCTGTTATTT | 146845 |
| rs183595641 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9613383 | TCATTTCATGAAGTT[A/G]GTCAGTTTTTGCTCT | 146845 |
| rs183608062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9583671 | ATACTATCTCACTAA[A/G]AACACAATCATGAAT | 146845 |
| rs183762473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9630132 | CTCACCCCTCATTAT[C/T]TTCCCCCTTATCCTA | 146845 |
| rs183765653 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607926 | TCCAGGCAATGTGTG[C/T]AGCACTGGCATGACT | 146845 |
| rs183773903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9588001 | ACCTTCCAAGAGTCC[A/G]ATTTGATTGGCCTGA | 146845 |
| rs183814932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9637040 | ACAGAGTGAGACTTC[G/T]TATCAAAAAAGCAAA | 146845 |
| rs183889024 | snp | A/G/T | 0.00974668 | 0.0691314 | upstream-variant-2KB, missense, nc-transcript-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575795 | CCCGGGACTCACCAG[A/G/T]GGTCCGGTGCCATCC | 146845 |
| rs183904330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9606436 | AAATGGTATCTGTCA[A/G]TAAATGCTGATGTGT | 146845 |
| rs183930211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CFAP52, STX8 | GRCh38.p7 | 17:9577903 | TCGAGACCATCCTGT[C/T]CAACATGGTGAAATC | 146845 |
| rs183970038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9609368 | ATGGAGAAAAATGAA[A/G]TAGGATGCAGAGTAA | 146845 |
| rs183989501 | snp | A/G | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9633673 | ACGAATTGTCATCTT[A/G]TCTTTTTTTTTTTTT | 146845 |
| rs184005755 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CFAP52 | GRCh38.p7 | 17:9611227 | AGTCTGTATCCTAGG[C/G]CCTCATTCATGTATA | 146845 |
| rs184009440 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CFAP52 | GRCh38.p7 | 17:9591074 | TGGAGTTTCACTCTT[A/G]TTTCCCAGGCTGGAG | 146845 |
| rs184032397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9597446 | TTTGCTATTCTACAA[C/T]GTGTATATGTATATA | 146845 |
| rs184053410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9589499 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATTAC | 146845 |
| rs184112297 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9640800 | AGGTGTGTGCCACCA[C/T]ATCCAGCTAATTTTT | 146845 |
| rs184113890 | snp | A/C | | | intron-variant | CFAP52 | GRCh38.p7 | 17:9622202 | TTTAACACATCAATC[A/C]CCTTAGATTCTTTTT | 146845 |
| rs184127925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9632209 | CAGCCTCCCGAGTAG[C/G]TAGGACTAAATGGGC | 146845 |
| rs184228310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9595523 | TCAGATTTGCAGAGT[C/G]ATTTGACTAAGCCAG | 146845 |
| rs184306700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9612160 | GGTACACCAACTTGT[A/G]AGTAACTCCTGCCTT | 146845 |
| rs184317386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9592261 | TGAGGTCAGGAGTTC[A/G]AGAACAGCCCGGCCA | 146845 |
| rs184325874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9626800 | AGTCCATCATTATAA[C/T]TGTAACACTAAGCCC | 146845 |
| rs184326223 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9578994 | GGTATAATGAGGCAT[G/T]TCTGACCTCCCATTC | 146845 |
| rs184358806 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CFAP52 | GRCh38.p7 | 17:9614376 | GGCCCAGCTGGTCGC[A/C/G]AGCTCCCAACCTCAG | 146845 |
| rs184378887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581148 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACCAA | 146845 |
| rs184539534 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9615554 | TTGGTTCCGTTTTAA[C/T]CTTTGCTGCATACAA | 146845 |
| rs184545559 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CFAP52 | GRCh38.p7 | 17:9596724 | TGTGTGTGTGTGTGT[G/T]TTTTTTTTGAGATGG | 146845 |
| rs184553373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581493 | TGATATGAGCCTATT[A/T]CAGTTTAAAGTGTAC | 146845 |
| rs184560330 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CFAP52 | GRCh38.p7 | 17:9627006 | TTTATACTTATGAAC[A/C]AAATGGTCTTTATTG | 146845 |
| rs184572959 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CFAP52 | GRCh38.p7 | 17:9585530 | AAAAAAATTAGCCAG[A/G]TGTGGTGGCGGGTGC | 146845 |
| rs184697124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9602359 | AACTCTCACTTATGA[A/G]TGAGAACATGCGGTG | 146845 |
| rs184834287 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CFAP52 | GRCh38.p7 | 17:9581741 | GTAGGAGCTGGTTCT[A/C]TTGCTTTAGTGAGAG | 146845 |
| rs184843443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9607040 | GTCACTAGCTATACT[A/G]AATGTTTTAAAATCA | 146845 |
| rs184944961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CFAP52 | GRCh38.p7 | 17:9629818 | TGGTCTTGAACTCCC[A/G]ACCTCAGGCAATCCA | 146845 |
| rs184955267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CFAP52 | GRCh38.p7 | 17:9587862 | GTTCTCTCTTGGCCC[A/G]TCTGTATTTCAGTAT | 146845 |
| rs185044778 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CFAP52, STX8 | GRCh38.p7 | 17:9575647 | GCGGGATGTGGCTGA[A/G]CCCCCTCAGTAAAGG | 146845 |