| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs6558298 | snp | C/T | 0.192401 | 0.243274 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101110 | aaagtgctgggatga[C/T]aggcgtgagccaccg | 81858 |
| rs6558299 | snp | A/G | 0.0887219 | 0.191022 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102494 | GACCAGGCTGGTCTC[A/G]AACTCCTGACATCAG | 81858 |
| rs11136254 | snp | A/C | 0.100088 | 0.200066 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103600 | AGCGCGGACCCTGAG[A/C]GGCCTGGGCGCTTCC | 81858 |
| rs11136255 | snp | A/G | 0.311123 | 0.242413 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104196 | GACCTCCAATGGGCT[A/G]CCACCTTCGCCCGCA | 81858 |
| rs11136256 | snp | C/T | 0.0298051 | 0.118382 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105743 | GCTGACTGTGGAGAC[C/T]GGAGATGCCCACATC | 81858 |
| rs11335429 | in-del | -/C | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104806 | ACCGACGCGGAGCGA[-/C]CCAGCCCAGCCAGAC | 81858 |
| rs11433813 | in-del | -/T | 0.447421 | 0.153379 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102275 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 81858 |
| rs11541802 | snp | C/G | | | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099566 | TCCGCCGCGTCCTCT[C/G]CACACGTTGCCCTGC | 81858 |
| rs11541803 | snp | C/T | | | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099339 | CCATCCTGCCGAACC[C/T]CGTAAGAGGCAAGGC | 81858 |
| rs11541804 | snp | C/G | 0.108282 | 0.205951 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099354 | CCGTAAGAGGCAAGG[C/G]TGCGCTCAGGCACAC | 81858 |
| rs11541805 | snp | C/T | 0.0542423 | 0.156054 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100007 | GTCTCCCTGCCCAGT[C/T]CCCCGGAAGCCTCCA | 81858 |
| rs11541806 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103575 | GCTTCCGGCTGGAGC[C/T]GCTGGGCGCGGGACC | 81858 |
| rs11546145 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104713 | GGATACAGTGCGGCC[C/T]GAGCGGAGGCCGCGG | 81858 |
| rs12549149 | snp | C/T | 0.101703 | 0.201266 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103543 | CCGCGCGCCCTCCGC[C/T]CCCACTCACCGCCCC | 81858 |
| rs12550729 | snp | C/T | 0.204189 | 0.245767 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100505 | AGCCACTGCCCTGGG[C/T]GTCTTCAGAGCTGAG | 81858 |
| rs13254954 | snp | A/G | 0.21695 | 0.247806 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098235 | GGTGTCCTAGCTGCA[A/G]GAGCTGAGGGGAGTG | 81858 |
| rs17852938 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105704 | GCTATTGGAGAACTC[A/G]AGCTTTGAAGCCATC | 81858 |
| rs34173062 | snp | A/G | 0.146162 | 0.227415 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103704 | AAGAGCACTGCGGCG[A/G]AGCCCAAGTCCGAGG | 81858 |
| rs34270727 | in-del | -/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101404 | TTTTTTTTTTTTTTT[-/T]GTGAGATGGAGTCTC | 81858 |
| rs34674752 | snp | A/G | 0.0583163 | 0.160491 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099319 | AGTAGAGGAAAGCAG[A/G]GTCCCCATCCTGCCG | 81858 |
| rs34818837 | in-del | -/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102217 | CTGGGTGAGAGAGGG[-/G]AGTCTTTGTCTGCAA | 81858 |
| rs34839093 | snp | A/G | 0.000234828 | 0.0108332 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099392 | CCGTCCGATGACCCA[A/G]CGTTGCACGGCTGGC | 81858 |
| rs34857822 | in-del | -/A | | | frameshift-variant, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099930 | CCCCCACCTGTACCT[-/A]CTCTCCGTCAAGTTT | 81858 |
| rs34947229 | in-del | -/A | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102935 | CTCCACCTACTCCCT[-/A]CCTGGAAGCCTTCCC | 81858 |
| rs34948990 | snp | A/G | 0.00914312 | 0.0669923 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098555 | TGGCTGGGGAGCCCC[A/G]CCTGCTGATGAGGGC | 81858 |
| rs34960192 | snp | A/G/T | 0.000428471 | 0.0146309 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098850 | CCACCTCCCCTGCCT[A/G/T]TGCCACCTCTGGTAC | 81858 |
| rs35333153 | in-del | -/T | 0 | 0 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100854 | CTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC | 81858 |
| rs35351724 | snp | A/G | 0.0854556 | 0.188216 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098292 | GCTGAATGGGAGAAA[A/G]GTGGTACCAATAGGC | 81858 |
| rs35397593 | snp | A/C/T | 0.0104709 | 0.0715948 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098504 | CTGACCACTGAGGCT[A/C/T]AGGGTCCGGGCCCAT | 81858 |
| rs35801151 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098267 | TGGCCATAGTCCAAG[C/G]AAGGCAAGAGCTGAA | 81858 |
| rs35844464 | snp | A/C/G | 0.00456515 | 0.0475596 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099196 | GGGTGCTGAGGGCTA[A/C/G]GTCCTGTGGCTGAGG | 81858 |
| rs57151029 | in-del | -/AG | 0.375 | 0.216506 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101602 | TTTTTTTTTTTTAGT[-/AG]AGTCAGGGTTTCACC | 81858 |
| rs57242566 | snp | A/G | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102865 | CTGGCTGGGGCCTCA[A/G]ATGGTGTAGGAGACT | 81858 |
| rs58173496 | in-del | -/T | 0 | 0 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101599 | TTTTTTTTTTTTTTT[-/T]AGTAGTCAGGGTTTC | 81858 |
| rs61732529 | snp | C/T | 0.000232994 | 0.0107909 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099154 | GATGGGGGAAACAAG[C/T]GTCCAAGTTCCCCGT | 81858 |
| rs66878813 | in-del | -/CTT/TCT | 0 | 0 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105299 | GTGGCTGGAGCTCTT[-/CTT/TCT]TTGGAGTGGGCGTGG | 81858 |
| rs71516044 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, frameshift-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106091 | ACTCAGCAAAAGCCA[-/A]GGCGGTGAGGAGGAG | 81858 |
| rs72543665 | in-del | -/CTT | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105301 | GGTGGCTGGAGCTCT[-/CTT]TYTGGAGTGGGCGTG | 81858 |
| rs73381305 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101671 | TCTGCCCACATCGGC[C/T]TCCCAAAGTGCTGTG | 81858 |
| rs73717808 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098534 | TTCTTCAGTAACACC[A/G]GGGTCTGGCTGGGGA | 81858 |
| rs74667328 | snp | A/C | 0.0726307 | 0.176182 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104142 | GCATCCAGCGTGCGA[A/C]TATCCCAGCGCCTAA | 81858 |
| rs75361772 | snp | A/G | 0.0696718 | 0.173152 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104401 | AGAAGGCAGAACTGA[A/G]TGGCGGGTACGGCAC | 81858 |
| rs76065466 | snp | C/G | 0.0197687 | 0.0974348 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103986 | TGGGCGAGGCTGGCG[C/G]CGTGTACGAGGCTGG | 81858 |
| rs76483965 | in-del | -/TCT | 0.0905309 | 0.192535 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105298 | CATGGTGGCTGGAGC[-/TCT]TCTTTTGGAGTGGGC | 81858 |
| rs76591178 | snp | A/G | 0.00580766 | 0.0535733 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099669 | ACCTGGGATGGTCAC[A/G]AGGACAAGGTGAAGA | 81858 |
| rs76889608 | snp | C/T | | | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099135 | GCCTGGGGGTAGCCC[C/T]AATGATGGGGGAAAC | 81858 |
| rs77359862 | snp | A/G | 0.0056191 | 0.0527065 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099379 | GCACACACAGGCACC[A/G]TCCGATGACCCAGCG | 81858 |
| rs78648437 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106165 | TGATTGCCACGCTCA[A/G]TGAGTCCTTCAGGCC | 81858 |
| rs111322040 | snp | A/G | 0 | 0 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100578 | CCCACTGCAATGGGG[A/G]GGTCCCCATCCAGTG | 81858 |
| rs112028217 | snp | A/G | 0.0178098 | 0.0926698 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098481 | AGAGATCCCCATGCC[A/G]TGCTTTCCTGACCAC | 81858 |
| rs112063891 | snp | A/G | | | splice-donor-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103049 | CATTACAGGGCACTG[A/G]CCATTCTGTCCTTCC | 81858 |
| rs112255220 | snp | C/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105443 | GGCTGACCTGGAGCC[C/T]GGACTTACCACCCTC | 81858 |
| rs112342688 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105302 | GGTGGCTGGAGCTCT[C/T]TTGGAGTGGGCGTGG | 81858 |
| rs112552278 | snp | C/T | 0.0161031 | 0.0882736 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098948 | ATCTCACAGCCAGGG[C/T]GGTCTGGGGCATTGA | 81858 |
| rs112813219 | snp | A/G | | | splice-donor-variant | SHARPIN | GRCh38.p7 | 8:144099701 | GCAGCCCCAGGCCTC[A/G]CCTGATGGGGCCAGG | 81858 |
| rs113068322 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105866 | TCTCTCTGCATCCTA[C/T]AGGATTGAGAGCTAC | 81858 |
| rs113151355 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104998 | GGCCCAGGCGGGCGC[C/T]GCCTGGTGACTGCAG | 81858 |
| rs113194942 | snp | C/G/T | 0 | 0 | utr-variant-3-prime, splice-donor-variant, downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098636 | TGAAAGGGATGCTTG[C/G/T]TGGCTCTTAAGGGTC | 81858 |
| rs113197734 | snp | G/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103048 | CCATTACAGGGCACT[G/T]ACCATTCTGTCCTTC | 81858 |
| rs113472943 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104035 | CTCACGTTAGAGCTG[G/T]TCTTTGGGGGCGAAG | 81858 |
| rs113734637 | snp | C/T | 0.0029089 | 0.0380262 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099773 | GATGCTGGGCCAGGA[C/T]GGCTGCCACTTGGGC | 81858 |
| rs113993743 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103421 | TCACCCCCATTTCAC[C/G]GACGAGAAAACAGAA | 81858 |
| rs114433070 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098225 | TTTCATTGCTGGTGT[C/T]CTAGCTGCAAGAGCT | 81858 |
| rs116004300 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102055 | CATGTTTCTCAGTCT[C/T]AACTGCTAACTCTTC | 81858 |
| rs117299156 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100763 | GGTTTGTTTGCTGCT[C/T]CCTTGGTCACATGGT | 81858 |
| rs117580205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102159 | CACCGTAGACCAGGA[A/G]TTCAAGGCTCCAGTG | 81858 |
| rs118008466 | snp | A/G | 0.000116491 | 0.00763098 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103111 | GCTGAGCTTCCTGAG[A/G]GTTGAGGAAGTGCAG | 81858 |
| rs138032964 | snp | A/C/G | 0.00279258 | 0.0372817 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104996 | GTGGCCCAGGCGGGC[A/C/G]CTGCCTGGTGACTGC | 81858 |
| rs138355198 | snp | C/G/T | 0.0287284 | 0.116357 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103902 | GCGCCGAGTGGTGCA[C/G/T]TCTGGCCAAGCCTGC | 81858 |
| rs138633295 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098138 | ACATGACCCAGCACC[A/G]GCCCAGTGACCTGGT | 81858 |
| rs139701481 | snp | C/T | 3.30896e-05 | 0.00406739 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105722 | CTTTGAAGCCATCAA[C/T]TCACAGCTGACTGTG | 81858 |
| rs139962028 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101534 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAT | 81858 |
| rs140040594 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100871 | AGACGGAGTTTCACT[C/T]GTTGCCCAGGCTGGA | 81858 |
| rs140042949 | snp | C/T | 1.66021e-05 | 0.0028811 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105966 | CTGGAGGCACTTTCT[C/T]CACCCCAGACTTCAG | 81858 |
| rs140326885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102999 | TCCCCAACCAGGACT[C/G]GGGGGCCAAGGCTAT | 81858 |
| rs141201044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100627 | TCTCAGGCCCACTAT[A/G]TTCTACCATCTCCCT | 81858 |
| rs141573856 | snp | C/T | 0.000682145 | 0.0184555 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105859 | TCATGGTTCTCTCTG[C/T]ATCCTATAGGATTGA | 81858 |
| rs143553694 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105525 | CCTGATGTGCAGCCT[A/G]GACAGAGGCCAGACT | 81858 |
| rs143866381 | snp | A/G | 0.00185283 | 0.0303806 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100099 | TGGGTGTGCTGTGCT[A/G]TGGCCTCTGTCCAGG | 81858 |
| rs144006632 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100993 | GGCATGCACCACCAC[A/G]CCCGGCTAATTTTGT | 81858 |
| rs144249942 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102568 | GTGAGCCACCCCACC[C/T]GGCCACTAATTCCAT | 81858 |
| rs144735402 | snp | C/T | 0.000348597 | 0.0131976 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105947 | GGAGGGCCAGCCCCA[C/T]GTGCTGGAGGCACTT | 81858 |
| rs145431068 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103325 | GACCATTTACACGGT[C/G]CTAAGCCCTGTACGC | 81858 |
| rs145525277 | snp | A/G | 0.000708156 | 0.0188036 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098911 | AAGGGGGTCCCAAGT[A/G]CAGGGCCTCTGGGTG | 81858 |
| rs145703823 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102076 | CTAACTCTTCCATTT[A/C]AGCAGCCATGTGAGC | 81858 |
| rs146582662 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102848 | GGAGGCTGCAACTTG[A/T]GCTGGCTGGGGCCTC | 81858 |
| rs146947779 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104955 | CTGGGATTTGTAGTT[C/G]CACCGCGGCTTGGCT | 81858 |
| rs147294629 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105579 | TTAGTGGGTAGGAGG[A/G]CTGAAGGCAGGGCCC | 81858 |
| rs147378643 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100734 | CAAGGATCACTTATA[C/T]ATGCTCACCTCAGGG | 81858 |
| rs148205171 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100596 | TCCCCATCCAGTGCT[A/G]ACACAGCTCCCGTGG | 81858 |
| rs148781318 | snp | C/T | 0.00245598 | 0.0349565 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105644 | TCACTCCCCAGGCAA[C/T]ACTAGCCCCTCTGGA | 81858 |
| rs149246735 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104151 | GTGCGACTATCCCAG[C/T]GCCTAACGGCAGCTG | 81858 |
| rs149544330 | snp | A/C | 0.000119899 | 0.00774178 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099484 | CTCCTCTGCCCCTGG[A/C]AGGGCTCCCCAGACC | 81858 |
| rs150179957 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103788 | CACCCCTCCGAGCGC[A/G]CTTCCGTGGGATCGG | 81858 |
| rs150993337 | snp | A/C | 0.000381534 | 0.0138066 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103563 | CTCACCGCCCCAGGT[A/C]CCGCGCCCAGCAGCT | 81858 |
| rs180734534 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104131 | CGGACGTAGATGCAT[C/T]CAGCGTGCGACTATC | 81858 |
| rs180866062 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100667 | AGCAGGGCCTTCCAC[A/G]CACCCAGCGCTGTTC | 81858 |
| rs181377031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098854 | CTCCCCTGCCTGTGC[C/G]ACCTCTGGTACCTCT | 81858 |
| rs182009566 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105115 | TTCCTCTCCCCGGGC[A/C]AGAAAGTAGCCAAAA | 81858 |
| rs182638894 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102005 | CTCGTTTGTGGGCTG[C/T]CCTCTATCTGGGAGC | 81858 |
| rs182704918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101468 | GGCTGGAGTGCAGTG[A/G]TGCAATCTCGGCTCA | 81858 |
| rs182784687 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100939 | CTCCTGGGTTCAGGC[A/G]ATTCTCCTGCCTCAG | 81858 |
| rs182918416 | snp | C/T | 0.000231888 | 0.0107652 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105758 | TGGAGATGCCCACAT[C/T]ATTGGCAGGTGAGGC | 81858 |
| rs184461229 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102364 | CTGCAACCTCTGCCT[C/G]CGGGTTCAAGTGATT | 81858 |
| rs184627197 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098631 | CACCATGAAAGGGAT[C/G]CTTGCTGGCTCTTAA | 81858 |
| rs184688195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103322 | ATAGACCATTTACAC[A/G]GTCCTAAGCCCTGTA | 81858 |
| rs185857366 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105381 | GGTGAGCAGGGTCCC[C/T]GGTGGTCTAGTCTAG | 81858 |
| rs186002508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100941 | CCTGGGTTCAGGCGA[G/T]TCTCCTGCCTCAGCC | 81858 |
| rs186039261 | snp | G/T | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104881 | TCCGCCCTGCGTCCC[G/T]CGCCGTCTGCGTACC | 81858 |
| rs187218299 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100696 | TCCTGGCCCCGGCCC[C/T]GGCCCCGGCCCCCAC | 81858 |
| rs187998311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101712 | TGAGCCACCGTGCCC[A/G]GCCCACTCAGCTAAT | 81858 |
| rs188600709 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098663 | GGTCTTTAATGGTTT[C/T]ATTTTGTGGCCCTTC | 81858 |
| rs188954031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102025 | TATCTGGGAGCCCCA[C/T]ACTACCTAGTCCTTC | 81858 |
| rs189221843 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102493 | TGACCAGGCTGGTCT[C/G]AAACTCCTGACATCA | 81858 |
| rs189603340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103334 | CACGGTCCTAAGCCC[C/T]GTACGCCTATCATCA | 81858 |
| rs189634832 | snp | C/T | 0.000102613 | 0.00716213 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099464 | GGCAGGTGATGTCAC[C/T]TAGGCTCCTCTGCCC | 81858 |
| rs190071341 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101388 | ATTACAGGCAGACAC[C/G]ACTACACTCAGCTAA | 81858 |
| rs190317757 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105550 | CAGACTCAGCTTGTT[C/G]CTAGCGGCTCCACTT | 81858 |
| rs190547150 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105074 | ACTAGGCAATTTTTC[C/T]GGGTAGAGTGGAGGA | 81858 |
| rs191764494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102533 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGAATTAC | 81858 |
| rs192013064 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100913 | TGATCTCGGCTCACC[A/G]CAACCTCCGCCTCCT | 81858 |
| rs192566318 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101851 | GCCAAAGGAGTACCT[A/G]GGACAGGGCAGCTGC | 81858 |
| rs192614290 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102126 | CAATAACAGCTACTT[A/C]GGCTGAAGCAGGAGG | 81858 |
| rs193045467 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098585 | CCTGTCTCCCTGTAT[C/T]GCTGGCTAGGATGGG | 81858 |
| rs199637644 | snp | C/T | 0.000159494 | 0.00892869 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103250 | GGGAGAGTCCAGGCT[C/T]AGGGCGTCCCCCCGC | 81858 |
| rs199738987 | snp | A/T | 0.00523954 | 0.0509312 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105770 | CATCATTGGCAGGTG[A/T]GGCAGGCTGGGGGGG | 81858 |
| rs199756474 | snp | A/G | 0.000200377 | 0.0100074 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099718 | CTGATGGGGCCAGGT[A/G]GGAAGCAGGCCTCCT | 81858 |
| rs199932176 | snp | A/C/G/T | 0.00607201 | 0.0548247 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099920 | CCAACCCCCTCCCCC[A/C/G/T]ACCTGTACCTCTCTC | 81858 |
| rs200051957 | snp | C/G | 0 | 0 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100014 | TTCCGGGGGACTGGG[C/G]AGGGAGACAGGGCAT | 81858 |
| rs200075787 | snp | A/C/G | 0.000533178 | 0.016319 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106080 | TGTCTGTGCAGACTC[A/C/G]GCAAAAGCCAAGGCG | 81858 |
| rs200222477 | snp | A/G | 1.79001e-05 | 0.00299161 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099120 | GGCAGCTGGCTGGGG[A/G]CCTGGGGGTAGCCCC | 81858 |
| rs200226522 | in-del | -/ACG | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102500 | CTGGTCTCAAACTCC[-/ACG]TGACATCAGGTGATC | 81858 |
| rs200240443 | snp | A/G/T | 3.32498e-05 | 0.00407725 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105640 | TCTCTCACTCCCCAG[A/G/T]CAATACTAGCCCCTC | 81858 |
| rs200314573 | snp | G/T | 0.00010008 | 0.00707319 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103160 | TCCTGGTGGAGGCTG[G/T]AGCTCGTGCTGGGTG | 81858 |
| rs200344062 | snp | C/T | 0.000303265 | 0.0123102 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099167 | AGCGTCCAAGTTCCC[C/T]GTCCATCTTCTGGGG | 81858 |
| rs200412533 | snp | A/G | 6.68617e-05 | 0.00578155 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099586 | GACGCGGCGGATGCG[A/G]CAGAGGCAGCGTCTT | 81858 |
| rs200449373 | snp | G/T | 0.00174701 | 0.0295035 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103054 | CAGGGCACTGACCAT[G/T]CTGTCCTTCCACGGT | 81858 |
| rs200607465 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101601 | TTTTTTTTTTTTTTA[A/G]TAGTCAGGGTTTCAC | 81858 |
| rs200617790 | snp | A/C/T | 3.63519e-05 | 0.0042632 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098831 | GTGGATTCTGCCCTG[A/C/T]CCCCCACCTCCCCTG | 81858 |
| rs200626709 | snp | A/G | 0.000338118 | 0.0129979 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099416 | GGCTGGCGGGAAACC[A/G]AGCTCTGAGAACACC | 81858 |
| rs200698932 | snp | C/G/T | 7.26353e-05 | 0.00602604 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099919 | CCCAACCCCCTCCCC[C/G/T]CACCTGTACCTCTCT | 81858 |
| rs200702253 | snp | C/G | 0.000218453 | 0.0104489 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099794 | CCACTTGGGCTGCCC[C/G]CTTCTCGTCTCCACC | 81858 |
| rs200764700 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102275 | AGCTAATTCCATCTT[C/T]TTTTTTTTTTTTTTT | 81858 |
| rs200777435 | snp | C/T | 3.35723e-05 | 0.00409695 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099393 | CGTCCGATGACCCAG[C/T]GTTGCACGGCTGGCG | 81858 |
| rs200797563 | snp | A/G | 0.000572005 | 0.0169019 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099801 | GGCTGCCCCCTTCTC[A/G]TCTCCACCTGCAATA | 81858 |
| rs200838839 | in-del | -/TG | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103919 | TGGCCAAGCCTGCCC[-/TG]CGCTGGCTTTGCCCA | 81858 |
| rs200972856 | snp | C/G | 0.00606514 | 0.0547338 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103611 | GGCCGCTCAGGGTCC[C/G]CGCTCAGCTGCAGCC | 81858 |
| rs201058020 | snp | C/T | 0.000251431 | 0.0112095 | missense, nc-transcript-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098934 | TCTGGGTGCTACACA[C/T]CTCACAGCCAGGGCG | 81858 |
| rs201069535 | snp | A/G/T | 6.91006e-05 | 0.0058776 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100003 | AGTGTGGAGGCTTCC[A/G/T]GGGGACTGGGCAGGG | 81858 |
| rs201083501 | snp | A/G | 3.52162e-05 | 0.00419605 | stop-gained, intron-variant | SHARPIN | GRCh38.p7 | 8:144099188 | TCTTCTGGGGGTGCT[A/G]AGGGCTAGGTCCTGT | 81858 |
| rs201294290 | snp | C/T | 7.18791e-05 | 0.00599453 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100064 | GTGGTGAGTTGCTCT[C/T]GCTGCCTAGAGGTAA | 81858 |
| rs201305567 | snp | G/T | 0.000194307 | 0.00985473 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099087 | CGTGCCCACCTGGAG[G/T]GGACTGGGCAGGCTG | 81858 |
| rs201311129 | in-del | -/G | 0.0146672 | 0.084371 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100573 | CCAGCCCACTGCAAT[-/G]GGGGGGGTCCCCATC | 81858 |
| rs201340976 | snp | G/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101602 | TTTTTTTTTTTTTAG[G/T]AGTCAGGGTTTCACC | 81858 |
| rs201396757 | snp | A/G | 3.3355e-05 | 0.00408367 | stop-gained, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103159 | CTCCTGGTGGAGGCT[A/G]TAGCTCGTGCTGGGT | 81858 |
| rs201472074 | snp | A/G/T | 0.000698056 | 0.0186697 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105784 | GAGGCAGGCTGGGGG[A/G/T]GCTGGCATCTCGGAG | 81858 |
| rs201533448 | snp | C/T | 0.000133545 | 0.00817035 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099578 | GTGCAGAGGACGCGG[C/T]GGATGCGGCAGAGGC | 81858 |
| rs201622976 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100022 | GACTGGGCAGGGAGA[C/T]AGGGCATGCTTCTGG | 81858 |
| rs201668898 | snp | C/T | 0.000200468 | 0.0100097 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099584 | AGGACGCGGCGGATG[C/T]GGCAGAGGCAGCGTC | 81858 |
| rs201680301 | snp | C/G/T | 0.000848416 | 0.0205791 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105852 | GCATGCTTCATGGTT[C/G/T]TCTCTGCATCCTATA | 81858 |
| rs201794180 | in-del | -/GGA | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104043 | GAGCTGGTCTTTGGG[-/GGA]GGCGAAGGGTCAGGG | 81858 |
| rs201818510 | snp | C/T | 5.01601e-05 | 0.00500775 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098970 | GGGCATTGATGAAGG[C/T]GCAGGAAGGACAGGA | 81858 |
| rs202027460 | snp | A/G | 0.00102556 | 0.0226214 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103188 | GTGGGGCCTCGGATG[A/G]TGTAGGAAACTGACT | 81858 |
| rs202237019 | in-del | -/TA | 0.00557542 | 0.0525036 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101768 | GCCCTGTACTTATTT[-/TA]TATGTCTGCCTCCTC | 81858 |
| rs367915714 | in-del | -/TCT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102583 | CGGCCACTAATTCCA[-/TCT]TCTAAGCATCTCTAG | 81858 |
| rs367915936 | snp | C/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105421 | TCGCGTGTTCTGCAG[C/G]GGGTATGGCTGACCT | 81858 |
| rs368001164 | snp | C/G | 6.69445e-05 | 0.00578513 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098945 | CACATCTCACAGCCA[C/G]GGCGGTCTGGGGCAT | 81858 |
| rs368029645 | snp | C/G/T | 6.75235e-05 | 0.00581015 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099812 | TCTCGTCTCCACCTG[C/G/T]AATAGCCCGGGCCAG | 81858 |
| rs368088636 | snp | A/G | 0.000132926 | 0.00815139 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105643 | CTCACTCCCCAGGCA[A/G]TACTAGCCCCTCTGG | 81858 |
| rs368101996 | snp | C/T | 0.000151399 | 0.00869923 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099400 | TGACCCAGCGTTGCA[C/T]GGCTGGCGGGAAACC | 81858 |
| rs368179662 | snp | G/T | 0.000159987 | 0.00894248 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099017 | AAGAGAGACAGTTGT[G/T]GCTTCCCTGCTCTTT | 81858 |
| rs368180546 | snp | A/C | 0.000317066 | 0.012587 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099684 | GAGGACAAGGTGAAG[A/C]AGCAGCCCCAGGCCT | 81858 |
| rs368240296 | in-del | -/GGATG | 0.00119737 | 0.0244387 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101628 | TCACCGTGTTAGCCA[-/GGATG]GTCTCGATCTCTTAA | 81858 |
| rs368352063 | in-del | -/CT | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100347 | CCACCTCTCTTGGCT[-/CT]TTCTGCCAGCCAGGG | 81858 |
| rs368359275 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104489 | GGGCCGGGCCCGGCG[A/G]ACGCTTGTTGTTGTC | 81858 |
| rs368474715 | snp | C/T | 0.000132637 | 0.00814254 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105674 | AGCACGGAGCTCCTT[C/T]CCCAAAGACATGAAG | 81858 |
| rs368525413 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105717 | TCGAGCTTTGAAGCC[A/G]TCAACTCACAGCTGA | 81858 |
| rs368762041 | snp | A/C/G/T | 6.65941e-05 | 0.00577007 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105806 | ATCTCGGAGGTCACA[A/C/G/T]TGCCGCGCCCTTCAG | 81858 |
| rs369335155 | snp | C/T | 5.0234e-05 | 0.00501144 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099544 | ACAGTGCAGTGGGGG[C/T]GGACCTGCAGGGCAA | 81858 |
| rs369439940 | snp | A/G | 1.75013e-05 | 0.0029581 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099885 | TCACCACTGGGGACT[A/G]TCTGCTATCCCCGAA | 81858 |
| rs369801459 | snp | C/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106029 | CCTACCTGGGGCTGG[C/G]GGTTGAGGGGAGGTG | 81858 |
| rs369801761 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102181 | GCTCCAGTGAGTTAG[C/G]GTCACGCTACTGCAC | 81858 |
| rs369818264 | snp | A/G | 6.67813e-05 | 0.00577808 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099579 | TGCAGAGGACGCGGC[A/G]GATGCGGCAGAGGCA | 81858 |
| rs369907286 | snp | C/T | 1.66369e-05 | 0.00288412 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105878 | CTATAGGATTGAGAG[C/T]TACTCATGTAAGATG | 81858 |
| rs369972505 | snp | A/G | 1.70324e-05 | 0.00291821 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099987 | AGGTGGAGGGCCCTT[A/G]AGTGTGGAGGCTTCC | 81858 |
| rs370038355 | snp | A/G | 0.000143469 | 0.00846842 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099137 | CTGGGGGTAGCCCCA[A/G]TGATGGGGGAAACAA | 81858 |
| rs370043380 | snp | A/C | 0.00010046 | 0.00708662 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098942 | CTACACATCTCACAG[A/C]CAGGGCGGTCTGGGG | 81858 |
| rs370144263 | snp | A/G | 6.66145e-05 | 0.00577086 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106160 | CTACCTGATTGCCAC[A/G]CTCAATGAGTCCTTC | 81858 |
| rs370279302 | snp | C/T | 5.01299e-05 | 0.00500624 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099587 | ACGCGGCGGATGCGG[C/T]AGAGGCAGCGTCTTC | 81858 |
| rs370326103 | snp | A/G | 1.81013e-05 | 0.00300838 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100078 | TTGCTGCCTAGAGGT[A/G]AGATATGGGTGTGCT | 81858 |
| rs370670828 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099880 | AGCTGTCACCACTGG[A/G]GACTATCTGCTATCC | 81858 |
| rs370921402 | snp | C/T | 8.43932e-05 | 0.00649534 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099407 | GCGTTGCACGGCTGG[C/T]GGGAAACCGAGCTCT | 81858 |
| rs370985648 | snp | C/G | 3.33895e-05 | 0.00408579 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099708 | CAGGCCTCACCTGAT[C/G]GGGCCAGGTGGGAAG | 81858 |
| rs371026461 | snp | C/G | 0.000116536 | 0.00763244 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103121 | CTGAGGGTTGAGGAA[C/G]TGCAGGCTGAGGGTT | 81858 |
| rs371028402 | snp | A/C/G | 0.000173736 | 0.00931879 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100011 | GGCTTCCGGGGGACT[A/C/G]GGCAGGGAGACAGGG | 81858 |
| rs371056984 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104242 | CACGCCCACACGTCG[C/T]ACTAGGTTGGCCCGC | 81858 |
| rs371109675 | snp | A/G | 1.66743e-05 | 0.00288736 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099362 | GGCAAGGCTGCGCTC[A/G]GGCACACACAGGCAC | 81858 |
| rs371467612 | snp | G/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100903 | TGCAGTGGTGTGATC[G/T]CGGCTCACCGCAACC | 81858 |
| rs371475032 | snp | A/C | 1.71193e-05 | 0.00292564 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099474 | GTCACCTAGGCTCCT[A/C]TGCCCCTGGCAGGGC | 81858 |
| rs371603416 | snp | A/G | 0.000150184 | 0.00866426 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099675 | GATGGTCACGAGGAC[A/G]AGGTGAAGAAGCAGC | 81858 |
| rs371756677 | snp | A/G | 3.38335e-05 | 0.00411286 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099821 | CACCTGCAATAGCCC[A/G]GGCCAGGCTCCCTGC | 81858 |
| rs371792980 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104581 | CTGTGGCGGTCGGCG[A/G]CAGGTCGGTCGCGAG | 81858 |
| rs371970645 | snp | A/G | 1.65696e-05 | 0.00287828 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105681 | AGCTCCTTCCCCAAA[A/G]ACATGAAGCTATTGG | 81858 |
| rs372146490 | snp | A/G | 0.00013322 | 0.00816041 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105813 | AGGTCACACTGCCGC[A/G]CCCTTCAGTGGAACC | 81858 |
| rs372402828 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101088 | GATCTGCCCACCTCG[A/G]CCTCCCAAAGTGCTG | 81858 |
| rs372516788 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098759 | GGAGATGTCGGACTT[A/G]TGAGGGAAGGGCCAC | 81858 |
| rs372684534 | snp | A/G | 8.34759e-05 | 0.00645995 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099597 | TGCGGCAGAGGCAGC[A/G]TCTTCAAGTGTGACC | 81858 |
| rs372912217 | snp | A/G | 0.000339461 | 0.0130236 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099433 | GCTCTGAGAACACCT[A/G]TGGCCAGAGCATCAG | 81858 |
| rs373024962 | snp | C/T | 0.000166146 | 0.00911293 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105905 | GATGGCAGGAGACGA[C/T]AAACACATGTTCAAG | 81858 |
| rs373073956 | snp | A/G | 3.33907e-05 | 0.00408586 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099571 | GCAACGTGTGCAGAG[A/G]ACGCGGCGGATGCGG | 81858 |
| rs373174477 | snp | A/G | 0.000149635 | 0.00864841 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099341 | ATCCTGCCGAACCCC[A/G]TAAGAGGCAAGGCTG | 81858 |
| rs373179874 | snp | A/G | 0.000692674 | 0.0185972 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099925 | CCCCTCCCCCCACCT[A/G]TACCTCTCTCCGTCA | 81858 |
| rs373246564 | snp | C/T | 6.80897e-05 | 0.0058344 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099240 | GACTGTGGGGCTGCA[C/T]CCCACCTCCCACACC | 81858 |
| rs373467092 | snp | C/T | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098297 | ATGGGAGAAAGGTGG[C/T]ACCAATAGGCCTGCA | 81858 |
| rs373616094 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103838 | CGGTCGGAAACACGG[A/G]CCGCGAACCTGGGGT | 81858 |
| rs373630291 | snp | C/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105184 | TCCCAGGTGTCCTGG[C/T]TCCTAACCGGGATGC | 81858 |
| rs373727483 | snp | C/G/T | 8.35644e-05 | 0.00646344 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099375 | TCAGGCACACACAGG[C/G/T]ACCGTCCGATGACCC | 81858 |
| rs373735012 | snp | A/C | 9.98353e-05 | 0.00706454 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103074 | CCTTCCACGGTGGCA[A/C]CTCGGACTAGGACTG | 81858 |
| rs373798191 | snp | A/G | 3.34146e-05 | 0.00408732 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099583 | GAGGACGCGGCGGAT[A/G]CGGCAGAGGCAGCGT | 81858 |
| rs373839286 | snp | C/T | 3.34784e-05 | 0.00409122 | missense, nc-transcript-variant, stop-gained | SHARPIN | GRCh38.p7 | 8:144098943 | TACACATCTCACAGC[C/T]AGGGCGGTCTGGGGC | 81858 |
| rs373954379 | snp | A/G | 3.31901e-05 | 0.00407356 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105664 | GCCCCTCTGGAGCAC[A/G]GAGCTCCTTCCCCAA | 81858 |
| rs374034142 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105028 | GCGCCCCAGCGGGGC[C/G]GAGGGACCGCCCTCC | 81858 |
| rs374116632 | snp | A/G | 3.32585e-05 | 0.00407776 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106204 | ACTTCAGCACAGCCC[A/G]CAGCCATGAGTTCAG | 81858 |
| rs374254942 | snp | C/T | 3.34392e-05 | 0.00408883 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098960 | GGGCGGTCTGGGGCA[C/T]TGATGAAGGTGCAGG | 81858 |
| rs374306893 | snp | A/C | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102906 | GCCACTCCAAGTACT[A/C]CAAGCTACTCCAGGC | 81858 |
| rs374315256 | snp | A/C | 3.5895e-05 | 0.0042363 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103263 | CTCAGGGCGTCCCCC[A/C]GCCCTACATCGCACG | 81858 |
| rs374855089 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105799 | GGCTGGCATCTCGGA[A/G]GTCACACTGCCGCGC | 81858 |
| rs374972852 | snp | C/T | 3.41834e-05 | 0.00413407 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099848 | CTGCCAGCTCTTCTG[C/T]AGGGTAAGGAAAGGA | 81858 |
| rs375063113 | in-del | -/A | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100953 | GATTCTCCTGCCTCA[-/A]GCCTCCTGAGTAGCT | 81858 |
| rs375273226 | snp | A/G | 6.67858e-05 | 0.00577827 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099576 | GTGTGCAGAGGACGC[A/G]GCGGATGCGGCAGAG | 81858 |
| rs375442263 | snp | C/T | 1.67351e-05 | 0.00289263 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099755 | GAACACTCAGGGCCA[C/T]ACGATGCTGGGCCAG | 81858 |
| rs375767637 | snp | A/G | 1.66638e-05 | 0.00288645 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106117 | AGGAGGGCCCCCTCA[A/G]TGACAAGTGCAGCCG | 81858 |
| rs375767993 | snp | A/G | 6.7473e-05 | 0.00580792 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099408 | CGTTGCACGGCTGGC[A/G]GGAAACCGAGCTCTG | 81858 |
| rs375879516 | snp | G/T | 1.70208e-05 | 0.00291721 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099442 | ACACCTGTGGCCAGA[G/T]CATCAGGGCAGGTGA | 81858 |
| rs376013836 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101541 | AGCCTCCCGAGTAGC[C/T]GGGACTATAGGTCCC | 81858 |
| rs376015740 | snp | A/C/G/T | 3.42661e-05 | 0.00413909 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099477 | ACCTAGGCTCCTCTG[A/C/G/T]CCCTGGCAGGGCTCC | 81858 |
| rs376430556 | snp | G/T | 4.98998e-05 | 0.00499474 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105789 | AGGCTGGGGGGGCTG[G/T]CATCTCGGAGGTCAC | 81858 |
| rs376520557 | snp | C/T | 9.98752e-05 | 0.00706595 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099299 | TTCTCGAGGAGCTGA[C/T]AGCAAGTAGAGGAAA | 81858 |
| rs376683299 | snp | C/T | 5.04791e-05 | 0.00502365 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099964 | GGGCTCCTAGGAAGA[C/T]CTGCCTCAGGTGGAG | 81858 |
| rs376711205 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102914 | AAGTACTCCAAGCTA[C/T]TCCAGGCTCCACCTA | 81858 |
| rs376757668 | snp | C/T | 0.000182103 | 0.00954034 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105701 | GAAGCTATTGGAGAA[C/T]TCGAGCTTTGAAGCC | 81858 |
| rs377059880 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105369 | CAGCAGCCCCAGGGT[A/G]AGCAGGGTCCCCGGT | 81858 |
| rs377082592 | snp | C/T | 3.34431e-05 | 0.00408906 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099378 | GGCACACACAGGCAC[C/T]GTCCGATGACCCAGC | 81858 |
| rs377181483 | snp | C/G | 5.38488e-05 | 0.0051886 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099131 | GGGGGCCTGGGGGTA[C/G]CCCCAATGATGGGGG | 81858 |
| rs377463573 | snp | C/G | 3.34119e-05 | 0.00408715 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103171 | GCTGTAGCTCGTGCT[C/G]GGTGGGGCCTCGGAT | 81858 |
| rs377501207 | snp | A/G | 8.33326e-05 | 0.00645441 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106022 | GGTGGGGCCTACCTG[A/G]GGCTGGGGGTTGAGG | 81858 |
| rs377516994 | snp | A/G | 6.67601e-05 | 0.00577716 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099631 | AGCCTGTGCCAGAAT[A/G]TGGGTTCAGGGATGG | 81858 |
| rs377546812 | in-del | -/T | 0.364609 | 0.222182 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100840 | CTTCCCTGCCACCAC[-/T]TTTTTTTTTTTTTTG | 81858 |
| rs377585461 | snp | A/G | 6.69916e-05 | 0.00578717 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103010 | GACTGGGGGGCCAAG[A/G]CTATTCCAAATTGTA | 81858 |
| rs377598498 | snp | A/G | 3.32552e-05 | 0.00407756 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099334 | GGTCCCCATCCTGCC[A/G]AACCCCGTAAGAGGC | 81858 |
| rs386414271 | in-del | -/CTT | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105300 | TGGTGGCTGGAGCTC[-/CTT]TTTTGGAGTGGGCGT | 81858 |
| rs397753145 | in-del | -/AAG | 0 | 0 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105302 | CCACGCCCACTCCAA[-/AAG]AAGAGCTCCAGCCAC | 81858 |
| rs397958505 | in-del | -/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101424 | TTTTTTTTTTTTTTT[-/T]GTGAGATGGAGTCTC | 81858 |
| rs398010158 | in-del | -/G | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104808 | GGGTCTGGCTGGGCT[-/G]GGTCGCTCCGCGTCG | 81858 |
| rs398113126 | in-del | -/AG | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101604 | TTTTTTTTTTAGTAG[-/AG]TCAGGGTTTCACCGT | 81858 |
| rs527367704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100222 | TTCTCCCAGCCTTGG[C/T]TCTGGCAAGACCCTC | 81858 |
| rs527638837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101086 | GTGATCTGCCCACCT[C/G]GGCCTCCCAAAGTGC | 81858 |
| rs528034676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101705 | ACAGGTGTGAGCCAC[C/T]GTGCCCGGCCCACTC | 81858 |
| rs528048788 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104020 | AGGGCGGCCGAGGCG[C/G]TCACGTTAGAGCTGG | 81858 |
| rs528356654 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098780 | GAAGGGCCACTCTCC[C/T]CTTGTAACCTGTGGG | 81858 |
| rs528440761 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104344 | GTAAGCGGGTTAGTA[A/C]GACGAGAAGAGTGAC | 81858 |
| rs528632290 | snp | C/T | 1.66134e-05 | 0.00288208 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105650 | CCCAGGCAATACTAG[C/T]CCCTCTGGAGCACGG | 81858 |
| rs529398336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100384 | TCACAGCAGAACCAA[A/C]GCAGGCCCTCAGTGG | 81858 |
| rs529854800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102561 | TACAGGCGTGAGCCA[C/T]CCCACCCGGCCACTA | 81858 |
| rs529876217 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100607 | TGCTGACACAGCTCC[C/T]GTGGTCTCAGGCCCA | 81858 |
| rs531045960 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098722 | GCAGTCAGTAGAGGT[C/T]CCCGGAGTTCAGTGG | 81858 |
| rs531461088 | in-del | -/GCGT | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104133 | ACGTAGATGCATCCA[-/GCGT]GCGTGCGACTATCCC | 81858 |
| rs531557606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102465 | TTTTAGTAGAGACAG[A/G]GTTTCACCTTGCTGA | 81858 |
| rs531819911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101805 | TAAAAATGCAAGCTC[C/T]AATAGGATGGGGATG | 81858 |
| rs531973806 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099440 | GAACACCTGTGGCCA[C/G]AGCATCAGGGCAGGT | 81858 |
| rs532684429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102524 | GGTGATCACCCACCT[C/T]GGCCTCCCAAAGTGC | 81858 |
| rs532871584 | snp | A/G | 0.000649453 | 0.0180085 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099292 | CTGGGGCTTCTCGAG[A/G]AGCTGACAGCAAGTA | 81858 |
| rs533501411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100546 | ACTCACCTTCTTACC[C/T]GCCCTGTGAGGCCCA | 81858 |
| rs533661862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100966 | TCAGCCTCCTGAGTA[A/G]CTGGGATCACAGGCA | 81858 |
| rs533831931 | in-del | -/AAAC | 0.00119737 | 0.0244387 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098199 | CTAGGAAGGGAAGGA[-/AAAC]AAACACCCATTTTCA | 81858 |
| rs534044361 | snp | C/G/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101248 | ATTATTTTTGTTTTT[C/G/T]TTTTTGGAGACAGGA | 81858 |
| rs534199607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100587 | ATGGGGGGGTCCCCA[C/T]CCAGTGCTGACACAG | 81858 |
| rs534620830 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103420 | GTCACCCCCATTTCA[A/C]GGACGAGAAAACAGA | 81858 |
| rs534998362 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101668 | TGATCTGCCCACATC[A/G]GCCTCCCAAAGTGCT | 81858 |
| rs535014036 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104619 | TCTGTGGAAGGGGGC[A/G]AGGCTATGTCGCGGT | 81858 |
| rs535328764 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104136 | GTAGATGCATCCAGC[C/G]TGCGACTATCCCAGC | 81858 |
| rs535420467 | snp | G/T | 0.000234706 | 0.0108304 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099001 | CCAGCTGGGCTGGGG[G/T]AAGAGAGACAGTTGT | 81858 |
| rs535458328 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098539 | CAGTAACACCGGGGT[A/C]TGGCTGGGGAGCCCC | 81858 |
| rs535505993 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104690 | GTCGCCGCGGAGCTT[C/T]TTCCCCCGGATACAG | 81858 |
| rs535559043 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104670 | AGGGCCGGGAGTAAC[A/G]GGACGTCGCCGCGGA | 81858 |
| rs535570486 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104116 | GCCCCAGGGGCTCGG[C/G]GGACGTAGATGCATC | 81858 |
| rs535666509 | snp | C/T | 3.77444e-05 | 0.00434405 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099897 | ACTATCTGCTATCCC[C/T]GAACCCCCCAACCCC | 81858 |
| rs535770870 | snp | C/T | 1.68377e-05 | 0.00290148 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099403 | CCCAGCGTTGCACGG[C/T]TGGCGGGAAACCGAG | 81858 |
| rs535829435 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105154 | CGCCCGCCCAGGTGA[C/T]CGCAGGGCCCGGAGT | 81858 |
| rs535834939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101486 | CAATCTCGGCTCACT[A/G]CAAGCTCCACCTCCT | 81858 |
| rs535908828 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101497 | CACTGCAAGCTCCAC[C/T]TCCTGGGTTCACGCC | 81858 |
| rs536603239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102728 | CTCTTGGGATGATGT[C/T]TTCTCACACAGGTCC | 81858 |
| rs537207079 | snp | C/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098577 | GATGAGGGCCTGTCT[C/G/T]CCTGTATCGCTGGCT | 81858 |
| rs537612147 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104507 | GCTTGTTGTTGTCCG[A/G]CCGGGGGAGGCGGAG | 81858 |
| rs537939905 | snp | A/G | 0.00100336 | 0.0223757 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098949 | TCTCACAGCCAGGGC[A/G]GTCTGGGGCATTGAT | 81858 |
| rs538003890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101152 | TGCCACCGTTTTAAA[C/T]AGCAATCCTCCCAGC | 81858 |
| rs538413538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102011 | TGTGGGCTGCCCTCT[A/C]TCTGGGAGCCCCATA | 81858 |
| rs538845524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101301 | GAGTGCAGTGGCACG[A/G]TCACAGCTCACTGCA | 81858 |
| rs539568406 | snp | C/T | 0.000100612 | 0.00709196 | missense, nc-transcript-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098932 | CCTCTGGGTGCTACA[C/T]ATCTCACAGCCAGGG | 81858 |
| rs540497132 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104907 | GTACCCGGAACCACA[A/G]CCCCCAGCAGGCCTC | 81858 |
| rs540931816 | in-del | -/A | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104805 | CACCGACGCGGAGCG[-/A]CCCAGCCCAGCCAGA | 81858 |
| rs541030351 | snp | C/T | 0.000193817 | 0.00984231 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103637 | CAGCCTCCGCAGCTG[C/T]GCCTCGGCGTCTGGC | 81858 |
| rs541611117 | in-del | -/GGCCCC | 0.0131025 | 0.0798721 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100691 | GCTGTTCCTGGCCCC[-/GGCCCC]GGCCCCGGCCCCCAC | 81858 |
| rs541657469 | snp | G/T | 0.00119737 | 0.0244387 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103706 | GAGCACTGCGGCGGA[G/T]CCCAAGTCCGAGGCC | 81858 |
| rs541666307 | in-del | -/C | 0.00557542 | 0.0525036 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104279 | TGGTTACGGGGTCGA[-/C]CCCCCCTAGGGGGCG | 81858 |
| rs541846780 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098706 | GTGACTGTCCCAGCA[A/T]GCAGTCAGTAGAGGT | 81858 |
| rs541955212 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098202 | AGGAAGGGAAGGAAA[A/G]CACCCATTTTCATTG | 81858 |
| rs542277478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100276 | TAGTGCTGGAGCTGC[A/G]CTTAGTTCATATTTG | 81858 |
| rs542345391 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144104273 | GCCTCACTGGTTACG[A/G]GGTCGACCCCCCTAG | 81858 |
| rs542885760 | snp | C/T | 0.00127774 | 0.0252435 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099840 | CAGGCTCCCTGCCAG[C/T]TCTTCTGCAGGGTAA | 81858 |
| rs543186475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101610 | TTTTTAGTAGTCAGG[G/T]TTTCACCGTGTTAGC | 81858 |
| rs543243138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102986 | GGTGGATCCAACTTC[C/T]CCAACCAGGACTGGG | 81858 |
| rs543379604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102429 | CAGGCACACGCCACC[A/G]CGCCTGGCTAATTTT | 81858 |
| rs543874468 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104974 | CGCGGCTTGGCTGGT[G/T]CCCGACGTGGCCCAG | 81858 |
| rs543900754 | snp | G/T | | | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105783 | TGAGGCAGGCTGGGG[G/T]GGCTGGCATCTCGGA | 81858 |
| rs544172989 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105542 | ACAGAGGCCAGACTC[A/G]GCTTGTTCCTAGCGG | 81858 |
| rs544552634 | snp | C/T | 3.34018e-05 | 0.00408654 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099668 | GACCTGGGATGGTCA[C/T]GAGGACAAGGTGAAG | 81858 |
| rs544661719 | snp | A/G | 1.66233e-05 | 0.00288295 | upstream-variant-2KB, splice-acceptor-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105638 | GGTCTCTCACTCCCC[A/G]GGCAATACTAGCCCC | 81858 |
| rs544983392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100141 | TTGGTTTTCCAGGAC[C/T]TTTGCCTTCTCCCTC | 81858 |
| rs545512350 | snp | A/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102537 | CTCGGCCTCCCAAAG[A/T]GCTGGAATTACAGGC | 81858 |
| rs545587657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101684 | GCCTCCCAAAGTGCT[A/G]TGATTACAGGTGTGA | 81858 |
| rs545674096 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098753 | GGGCCTGGAGATGTC[A/G]GACTTGTGAGGGAAG | 81858 |
| rs545686101 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104337 | GCCGGGGGTAAGCGG[A/G]TTAGTACGACGAGAA | 81858 |
| rs545973264 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104848 | CGGCCTGATCTAACC[A/C]AGCCAGGCAGGTGGG | 81858 |
| rs546254240 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098500 | TTTCCTGACCACTGA[A/G]GCTCAGGGTCCGGGC | 81858 |
| rs546595353 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104352 | GTTAGTACGACGAGA[A/T]GAGTGACAGACAGGC | 81858 |
| rs546656540 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104029 | GAGGCGCTCACGTTA[C/G]AGCTGGTCTTTGGGG | 81858 |
| rs546802723 | snp | C/T | 6.64485e-05 | 0.00576366 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105651 | CCAGGCAATACTAGC[C/T]CCTCTGGAGCACGGA | 81858 |
| rs546841328 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105136 | GTAGCCAAAACGAAA[A/G]AGCGCCCGCCCAGGT | 81858 |
| rs546878969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098798 | TGTAACCTGTGGGGG[A/G]GGAGCTGGGTCATTC | 81858 |
| rs547664740 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100777 | TTCCTTGGTCACATG[A/G]TTCATGCCATGACCT | 81858 |
| rs547807104 | snp | C/G | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102784 | TGCTTGCCTCTCATC[C/G]TTCCTGAGGGTTAAG | 81858 |
| rs547991453 | snp | A/G | 1.81704e-05 | 0.00301411 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103274 | CCCCCGCCCTACATC[A/G]CACGAGGAGCAAAGA | 81858 |
| rs548436285 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100491 | CAGCACTCCAGACAA[A/G]CCACTGCCCTGGGCG | 81858 |
| rs549928490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101161 | TTTAAACAGCAATCC[C/T]CCCAGCTCCACCATT | 81858 |
| rs549976877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101816 | GCTCCAATAGGATGG[C/G]GATGGGAGGTTTTGT | 81858 |
| rs550269288 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100952 | CGATTCTCCTGCCTC[-/A]AGCCTCCTGAGTAGC | 81858 |
| rs550592820 | snp | A/G | 0.000533805 | 0.0163284 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099281 | CGAGGACTGACCTGG[A/G]GCTTCTCGAGGAGCT | 81858 |
| rs550621520 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104476 | ATTCAGAGGCGCGGG[A/G]CCGGGCCCGGCGGAC | 81858 |
| rs550902061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100405 | CCCTCAGTGGCCCTG[A/C]AGTCAGGGTGGCCTC | 81858 |
| rs551095847 | snp | G/T | 1.67253e-05 | 0.00289178 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099750 | AAGCTGAACACTCAG[G/T]GCCACACGATGCTGG | 81858 |
| rs551589838 | snp | C/T | 1.8136e-05 | 0.00301126 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100084 | CCTAGAGGTAAGATA[C/T]GGGTGTGCTGTGCTG | 81858 |
| rs551729674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100568 | TGAGGCCCAGCCCAC[G/T]GCAATGGGGGGGTCC | 81858 |
| rs551752885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100992 | AGGCATGCACCACCA[C/T]GCCCGGCTAATTTTG | 81858 |
| rs552332976 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105049 | ACCGCCCTCCTAGGC[A/G]TCTGGAGAAACTAGG | 81858 |
| rs552537225 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104511 | GTTGTTGTCCGGCCG[C/G]GGGAGGCGGAGGTCG | 81858 |
| rs552702150 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103499 | GCCTAACTTTGGGCT[C/T]CGTGCCCTGCCCGGG | 81858 |
| rs552933359 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098678 | CATTTTGTGGCCCTT[C/T]CCCCCAACCCTGGTG | 81858 |
| rs552935234 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104630 | GGGCGAGGCTATGTC[A/G]CGGTGGCAGCCCGGA | 81858 |
| rs552998379 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104205 | TGGGCTGCCACCTTC[A/G]CCCGCAGACCCCAGC | 81858 |
| rs553054724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103519 | CCCTGCCCGGGCCAA[G/T]AGGACTGACCGCGCG | 81858 |
| rs554047729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100703 | CCCGGCCCCGGCCCC[A/G]GCCCCCACTGAACCT | 81858 |
| rs554127010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144102097 | CCATGTGAGCCAGGG[A/G]CAGTGGCTCATGCCA | 81858 |
| rs554393647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102872 | GGGCCTCAGATGGTG[G/T]AGGAGACTGACTCCA | 81858 |
| rs554522364 | snp | C/T | 1.672e-05 | 0.00289132 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099747 | CTGAAGCTGAACACT[C/T]AGGGCCACACGATGC | 81858 |
| rs554921025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102990 | GATCCAACTTCCCCA[A/G]CCAGGACTGGGGGGC | 81858 |
| rs555189362 | snp | A/G | 0.00676609 | 0.0577691 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103566 | ACCGCCCCAGGTCCC[A/G]CGCCCAGCAGCTCCA | 81858 |
| rs555221400 | in-del | -/TCGC | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104523 | CGGGGGAGGCGGAGG[-/TCGC]TCGCTCGCTCGCTCG | 81858 |
| rs555274225 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104301 | TAGGGGGCGGAGCTA[C/G]AGAGGCCACGGCCAA | 81858 |
| rs555628524 | snp | C/T | 1.6666e-05 | 0.00288664 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106082 | TCTGTGCAGACTCAG[C/T]AAAAGCCAAGGCGGT | 81858 |
| rs555665685 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105521 | AGCTCCTGATGTGCA[C/G]CCTGGACAGAGGCCA | 81858 |
| rs555906602 | snp | G/T | | | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105857 | CTTCATGGTTCTCTC[G/T]GCATCCTATAGGATT | 81858 |
| rs555935290 | snp | A/G | 0.00012459 | 0.00789172 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099168 | GCGTCCAAGTTCCCC[A/G]TCCATCTTCTGGGGG | 81858 |
| rs556127279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100648 | CCATCTCCCTACTAG[A/G]ATAAGCAGGGCCTTC | 81858 |
| rs556517361 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101157 | CCGTTTTAAACAGCA[A/G]TCCTCCCAGCTCCAC | 81858 |
| rs556978793 | snp | C/T | 8.65194e-05 | 0.00657664 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099057 | ATGGCTGTCCTGGCC[C/T]TCCCTGCCCAGTCCC | 81858 |
| rs557065049 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098545 | CACCGGGGTCTGGCT[G/T]GGGAGCCCCGCCTGC | 81858 |
| rs557108256 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105163 | AGGTGACCGCAGGGC[C/G]CGGAGTCCCAGGTGT | 81858 |
| rs557382381 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104788 | CCCCGCCTGCGCACC[A/G]GCACCGACGCGGAGC | 81858 |
| rs558072764 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101953 | CTCTTACATCACTGT[C/T]TGGCTGTCTTCCTAC | 81858 |
| rs558184218 | snp | C/T | 3.42009e-05 | 0.00413513 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099472 | ATGTCACCTAGGCTC[C/T]TCTGCCCCTGGCAGG | 81858 |
| rs558294828 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105435 | GGGGGTATGGCTGAC[C/T]TGGAGCCTGGACTTA | 81858 |
| rs558322802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102300 | TTTTTTTGAGATGGA[A/G]TCTTGCTCTGTCACC | 81858 |
| rs558565345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102741 | GTCTTCTCACACAGG[A/T]CCTGACCCTGCCTGC | 81858 |
| rs559001796 | snp | C/T | 0.000798403 | 0.0199641 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103616 | CTCAGGGTCCGCGCT[C/T]AGCTGCAGCCTCCGC | 81858 |
| rs559380649 | snp | A/G | 0.00118483 | 0.0243108 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103655 | CTCGGCGTCTGGCCC[A/G]GCGCCCAGCGGCCTC | 81858 |
| rs559941971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100167 | CCCTCACCTCAGTCC[A/G]TGCCAGGGCCCTGCC | 81858 |
| rs560607879 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100889 | TGCCCAGGCTGGAGT[A/G]CAGTGGTGTGATCTC | 81858 |
| rs560669320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100382 | CCTCACAGCAGAACC[A/G]AAGCAGGCCCTCAGT | 81858 |
| rs560716966 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102365 | TGCAACCTCTGCCTC[C/T]GGGTTCAAGTGATTC | 81858 |
| rs560727610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101704 | TACAGGTGTGAGCCA[C/T]CGTGCCCGGCCCACT | 81858 |
| rs561297740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101727 | GGCCCACTCAGCTAA[G/T]TTTTAAATTTTTTGT | 81858 |
| rs561587842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102431 | GGCACACGCCACCAC[A/G]CCTGGCTAATTTTTG | 81858 |
| rs561699355 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104383 | TCCATAACCAGTAGA[C/T]GTAGAAGGCAGAACT | 81858 |
| rs561984365 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104931 | AGGCCTCGCGCGGCG[C/T]GCTGCCTCCTGGGAT | 81858 |
| rs562365868 | in-del | -/GGCCCCGGCCCC | 0.00160675 | 0.0282983 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100685 | CCCAGCGCTGTTCCT[-/GGCCCCGGCCCC]GGCCCCGGCCCCCAC | 81858 |
| rs562492626 | snp | C/T | 1.67038e-05 | 0.00288992 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099728 | CAGGTGGGAAGCAGG[C/T]CTCCTGAAGCTGAAC | 81858 |
| rs562533242 | snp | A/C | 1.66801e-05 | 0.00288787 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099283 | AGGACTGACCTGGGG[A/C]TTCTCGAGGAGCTGA | 81858 |
| rs563396079 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098709 | ACTGTCCCAGCAAGC[A/G]GTCAGTAGAGGTCCC | 81858 |
| rs563528580 | snp | C/T | 0.000736106 | 0.0191706 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103745 | CGCCCCGCCCGCTGG[C/T]GGCGCCATCTCCGGT | 81858 |
| rs563648983 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104299 | CCTAGGGGGCGGAGC[C/T]AGAGAGGCCACGGCC | 81858 |
| rs564281728 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100872 | GACGGAGTTTCACTC[-/G]TTGCCCAGGCTGGAG | 81858 |
| rs564360333 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104338 | CCGGGGGTAAGCGGG[G/T]TAGTACGACGAGAAG | 81858 |
| rs564435451 | snp | A/G | 1.78115e-05 | 0.0029842 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099112 | AGGCTGGAGGCAGCT[A/G]GCTGGGGGCCTGGGG | 81858 |
| rs565007645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101637 | TAGCCAGGATGGTCT[C/T]GATCTCTTAACCTCA | 81858 |
| rs565386743 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102147 | AAGCAGGAGGATCAC[C/T]GTAGACCAGGAGTTC | 81858 |
| rs565572316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102539 | CGGCCTCCCAAAGTG[C/T]TGGAATTACAGGCGT | 81858 |
| rs565829522 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105133 | AAAGTAGCCAAAACG[A/G]AAGAGCGCCCGCCCA | 81858 |
| rs566351279 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104130 | GCGGACGTAGATGCA[G/T]CCAGCGTGCGACTAT | 81858 |
| rs566907704 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100569 | GAGGCCCAGCCCACT[C/G]CAATGGGGGGGTCCC | 81858 |
| rs567754700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101129 | CGTGAGCCACCGCGC[A/C]CGGCCCCTGCCACCG | 81858 |
| rs567765786 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100626 | GTCTCAGGCCCACTA[C/T]ATTCTACCATCTCCC | 81858 |
| rs568347092 | snp | A/G/T | 5.13671e-05 | 0.00506768 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099852 | CAGCTCTTCTGCAGG[A/G/T]TAAGGAAAGGACAGC | 81858 |
| rs568386578 | snp | C/T | 5.39981e-05 | 0.00519578 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098841 | CCCTGCCCCCCACCT[C/T]CCCTGCCTGTGCCAC | 81858 |
| rs568434127 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105140 | CCAAAACGAAAGAGC[A/G]CCCGCCCAGGTGACC | 81858 |
| rs568718279 | snp | C/T | 6.62976e-05 | 0.00575712 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105677 | ACGGAGCTCCTTCCC[C/T]AAAGACATGAAGCTA | 81858 |
| rs568863338 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104491 | GCCGGGCCCGGCGGA[A/C]GCTTGTTGTTGTCCG | 81858 |
| rs569730111 | in-del | -/C | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103812 | GATCGGGCCGCTGAG[-/C]CCCCCTCCGCCGGTC | 81858 |
| rs569936293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102594 | TCCATCTTCTAAGCA[C/T]CTCTAGAAACATCCT | 81858 |
| rs570005869 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104648 | GTGGCAGCCCGGATG[A/G]GCCGGCAGGGCCGGG | 81858 |
| rs570197136 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104133 | GACGTAGATGCATCC[A/G]GCGTGCGACTATCCC | 81858 |
| rs570453030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102847 | TGGAGGCTGCAACTT[C/G]TGCTGGCTGGGGCCT | 81858 |
| rs570464489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103350 | GTACGCCTATCATCA[A/G]ATCCTCACAATAGCC | 81858 |
| rs570807510 | snp | A/G | 0.0151205 | 0.0856249 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104530 | AGGCGGAGGTCGCTC[A/G]CTCGCTCGCTCGGCT | 81858 |
| rs570830736 | snp | A/C | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098268 | GGCCATAGTCCAAGG[A/C]AGGCAAGAGCTGAAT | 81858 |
| rs570832649 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101063 | TGGTCTTGAACTCCC[A/G]ACCTCAGGTGATCTG | 81858 |
| rs571059518 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098935 | CTGGGTGCTACACAT[C/G]TCACAGCCAGGGCGG | 81858 |
| rs571318286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101226 | TAAAAAACTCTACAG[C/T]AATTTTATTATTTTT | 81858 |
| rs571714085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101842 | TTTGTTCATGCCAAA[A/G]GAGTACCTGGGACAG | 81858 |
| rs571752438 | snp | C/T | 0.000255936 | 0.0113094 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099238 | AGGACTGTGGGGCTG[C/T]ACCCCACCTCCCACA | 81858 |
| rs572016810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SHARPIN | GRCh38.p7 | 8:144101477 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAAGCT | 81858 |
| rs572312403 | in-del | -/C | 0.0080159 | 0.0627989 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104531 | GGCGGAGGTCGCTCG[-/C]TCGCTCGCTCGGCTC | 81858 |
| rs572422598 | snp | C/T | 0.00185326 | 0.0303841 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099273 | ACCCCCATCGAGGAC[C/T]GACCTGGGGCTTCTC | 81858 |
| rs572645076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102982 | GGAAGGTGGATCCAA[C/T]TTCCCCAACCAGGAC | 81858 |
| rs572750141 | snp | C/T | 0.000151522 | 0.00870275 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099806 | CCCCCTTCTCGTCTC[C/T]ACCTGCAATAGCCCG | 81858 |
| rs572758287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102416 | GTAGCTGGGACTACA[A/G]GCACACGCCACCACG | 81858 |
| rs573029115 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105437 | GGGTATGGCTGACCT[A/G]GAGCCTGGACTTACC | 81858 |
| rs573157145 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104888 | TGCGTCCCGCGCCGT[C/T]TGCGTACCCGGAACC | 81858 |
| rs573875084 | snp | A/G | 4.99322e-05 | 0.00499636 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106176 | CTCAATGAGTCCTTC[A/G]GGCCTGACTATGACT | 81858 |
| rs574460041 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104649 | TGGCAGCCCGGATGG[G/T]CCGGCAGGGCCGGGA | 81858 |
| rs574460088 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098701 | CCCTGGTGACTGTCC[C/T]AGCAAGCAGTCAGTA | 81858 |
| rs574572887 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104263 | GTTGGCCCGCGCCTC[A/T]CTGGTTACGGGGTCG | 81858 |
| rs575107274 | snp | G/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105556 | CAGCTTGTTCCTAGC[G/T]GCTCCACTTAGTGGG | 81858 |
| rs575371085 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104334 | AACGCCGGGGGTAAG[A/C/G]GGGTTAGTACGACGA | 81858 |
| rs575625315 | snp | A/C/T | 0.000105151 | 0.00725023 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099072 | CTCCCTGCCCAGTCC[A/C/T]GTGCCCACCTGGAGT | 81858 |
| rs575686517 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104800 | ACCGGCACCGACGCG[C/G]AGCGACCCAGCCCAG | 81858 |
| rs575944472 | snp | C/T | 4.99222e-05 | 0.00499586 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105862 | TGGTTCTCTCTGCAT[C/T]CTATAGGATTGAGAG | 81858 |
| rs576069602 | snp | A/C/G | 5.36278e-05 | 0.00517798 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103262 | GCTCAGGGCGTCCCC[A/C/G]CGCCCTACATCGCAC | 81858 |
| rs576711521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102994 | CAACTTCCCCAACCA[C/G]GACTGGGGGGCCAAG | 81858 |
| rs576797888 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103622 | GTCCGCGCTCAGCTG[A/C]AGCCTCCGCAGCTGT | 81858 |
| rs576882474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102316 | TCTTGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 81858 |
| rs576882614 | in-del | -/CTT | 0.00318978 | 0.0398085 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100206 | CACTTCTAGCCACAC[-/CTT]CTCCCAGCCTTGGCT | 81858 |
| rs577129971 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104160 | TCCCAGCGCCTAACG[A/G]CAGCTGGACTTCGCT | 81858 |
| rs577869302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100656 | CTACTAGGATAAGCA[A/G]GGCCTTCCACGCACC | 81858 |
| rs577870600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100125 | CCAGGCCTCTAGGCC[C/T]TTGGTTTTCCAGGAC | 81858 |
| rs578196723 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102186 | AGTGAGTTAGGGTCA[C/T]GCTACTGCACTCCAG | 81858 |
| rs745434380 | snp | A/G | 0.000348377 | 0.0131935 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105665 | CCCCTCTGGAGCACG[A/G]AGCTCCTTCCCCAAA | 81858 |
| rs745592037 | snp | A/G | 1.71761e-05 | 0.00293049 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099861 | TGCAGGGTAAGGAAA[A/G]GACAGCTGTCACCAC | 81858 |
| rs745718448 | snp | A/G | 1.71044e-05 | 0.00292436 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099048 | CCAATGCCCATGGCT[A/G]TCCTGGCCCTCCCTG | 81858 |
| rs745796766 | snp | C/G | 1.77436e-05 | 0.0029785 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099105 | ACTGGGCAGGCTGGA[C/G]GCAGCTGGCTGGGGG | 81858 |
| rs746004362 | snp | C/T | 1.66949e-05 | 0.00288915 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099674 | GGATGGTCACGAGGA[C/T]AAGGTGAAGAAGCAG | 81858 |
| rs746041158 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105107 | CTGTAGTTTTCCTCT[C/G]CCCGGGCCAGAAAGT | 81858 |
| rs746232418 | snp | C/T | 4.99946e-05 | 0.00499948 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106064 | GCCCAGCTGATGGTT[C/T]TGTCTGTGCAGACTC | 81858 |
| rs746278696 | snp | C/T | 1.81853e-05 | 0.00301535 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100104 | GTGCTGTGCTGTGGC[C/T]TCTGTCCAGGCCTCT | 81858 |
| rs746365862 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100138 | CCCTTGGTTTTCCAG[A/G]ACCTTTGCCTTCTCC | 81858 |
| rs746401235 | snp | C/T | 3.3253e-05 | 0.00407742 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099333 | GGGTCCCCATCCTGC[C/T]GAACCCCGTAAGAGG | 81858 |
| rs746401527 | snp | A/G | 1.66405e-05 | 0.00288443 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103079 | CACGGTGGCACCTCG[A/G]ACTAGGACTGCCCAC | 81858 |
| rs746462580 | snp | C/T | 1.81668e-05 | 0.00301381 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100088 | GAGGTAAGATATGGG[C/T]GTGCTGTGCTGTGGC | 81858 |
| rs746723710 | snp | C/T | 3.32127e-05 | 0.00407495 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105655 | GCAATACTAGCCCCT[C/T]TGGAGCACGGAGCTC | 81858 |
| rs746918471 | snp | A/G | 3.34566e-05 | 0.00408989 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098955 | AGCCAGGGCGGTCTG[A/G]GGCATTGATGAAGGT | 81858 |
| rs746973574 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098777 | AGGGAAGGGCCACTC[C/T]CCCCTTGTAACCTGT | 81858 |
| rs747099758 | snp | C/T | 7.47831e-05 | 0.00611441 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103525 | CCGGGCCAAGAGGAC[C/T]GACCGCGCGCCCTCC | 81858 |
| rs747101211 | snp | A/G | 1.74491e-05 | 0.00295368 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103235 | ATTAACCTGAGAAGA[A/G]GGAGAGTCCAGGCTC | 81858 |
| rs747172393 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103327 | CCATTTACACGGTCC[C/T]AAGCCCTGTACGCCT | 81858 |
| rs747258304 | snp | C/T | 5.01081e-05 | 0.00500515 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099575 | CGTGTGCAGAGGACG[C/T]GGCGGATGCGGCAGA | 81858 |
| rs747427525 | snp | A/T | 1.66123e-05 | 0.00288199 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105916 | ACGACAAACACATGT[A/T]CAAGCAGTTCTGCCA | 81858 |
| rs747441138 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104097 | AGGCGGACGCGGCCT[C/T]TTCGCCCCAGGGGCT | 81858 |
| rs747549689 | snp | C/T | 1.76839e-05 | 0.00297349 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099926 | CCCTCCCCCCACCTG[C/T]ACCTCTCTCCGTCAA | 81858 |
| rs747550327 | snp | A/C/T | 3.33224e-05 | 0.0040817 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106051 | GGGGAGGTGATGGGC[A/C/T]CAGCTGATGGTTCTG | 81858 |
| rs747573095 | snp | A/C/G | 5.06388e-05 | 0.00503162 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103193 | GCCTCGGATGGTGTA[A/C/G]GAAACTGACTCCAGG | 81858 |
| rs747634446 | snp | C/T | 3.32342e-05 | 0.00407627 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105902 | TAAGATGGCAGGAGA[C/T]GACAAACACATGTTC | 81858 |
| rs747773365 | snp | G/T | 3.51062e-05 | 0.00418949 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099215 | CTGTGGCTGAGGGGG[G/T]GGAGCTCAGGACTGT | 81858 |
| rs747797971 | in-del | -/G | 1.6696e-05 | 0.00288924 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105779 | CAGGTGAGGCAGGCT[-/G]GGGGGGCTGGCATCT | 81858 |
| rs747883788 | in-del | -/A | 3.42521e-05 | 0.00413822 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099854 | GCTCTTCTGCAGGGT[-/A]AGGAAAGGACAGCTG | 81858 |
| rs747952143 | snp | A/G | | | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099978 | ATCTGCCTCAGGTGG[A/G]GGGCCCTTGAGTGTG | 81858 |
| rs748175578 | snp | C/T | 1.68604e-05 | 0.00290343 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099027 | GTTGTTGCTTCCCTG[C/T]TCTTTCCAATGCCCA | 81858 |
| rs748211287 | snp | C/G | 1.66125e-05 | 0.00288201 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106219 | GCAGCCATGAGTTCA[C/G]CCGGGAGCCCAGCCT | 81858 |
| rs748389296 | snp | A/C | 1.71443e-05 | 0.00292777 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103212 | ACTGACTCCAGGGGC[A/C]ACTCCAAATTAACCT | 81858 |
| rs748466081 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104283 | TTACGGGGTCGACCC[A/C]CCTAGGGGGCGGAGC | 81858 |
| rs748567191 | snp | C/G | 3.33901e-05 | 0.00408582 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099570 | GGCAACGTGTGCAGA[C/G]GACGCGGCGGATGCG | 81858 |
| rs748630931 | snp | A/G | 1.66427e-05 | 0.00288462 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105846 | GGGGAAGCATGCTTC[A/G]TGGTTCTCTCTGCAT | 81858 |
| rs748742689 | snp | A/C/G | 0.000199594 | 0.00998785 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099310 | CTGACAGCAAGTAGA[A/C/G]GAAAGCAGGGTCCCC | 81858 |
| rs748840660 | snp | A/G | 1.72612e-05 | 0.00293774 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099869 | AAGGAAAGGACAGCT[A/G]TCACCACTGGGGACT | 81858 |
| rs748959417 | snp | A/C | 3.63062e-05 | 0.00426049 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099921 | CAACCCCCTCCCCCC[A/C]CCTGTACCTCTCTCC | 81858 |
| rs748973820 | snp | C/G | | | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100046 | CTTCTGGGCCCAAGG[C/G]TGGTGGTGAGTTGCT | 81858 |
| rs748993857 | in-del | -/GG | 1.67624e-05 | 0.00289498 | frameshift-variant, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099539 | CTGCAACAGTGCAGT[-/GG]GGGTGGACCTGCAGG | 81858 |
| rs749282187 | snp | A/C | 7.26401e-05 | 0.00602617 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103537 | GACTGACCGCGCGCC[A/C]TCCGCCCCCACTCAC | 81858 |
| rs749314419 | snp | C/G | 3.39219e-05 | 0.00411823 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099775 | TGCTGGGCCAGGACG[C/G]CTGCCACTTGGGCTG | 81858 |
| rs749540271 | snp | C/T | 1.66388e-05 | 0.00288429 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106184 | GTCCTTCAGGCCTGA[C/T]TATGACTTCAGCACA | 81858 |
| rs749606288 | snp | A/G | 1.66388e-05 | 0.00288429 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103101 | ACTGCCCACCGCTGA[A/G]CTTCCTGAGGGTTGA | 81858 |
| rs749678393 | snp | C/T | 5.10617e-05 | 0.00505255 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103202 | GGTGTAGGAAACTGA[C/T]TCCAGGGGCCACTCC | 81858 |
| rs749884925 | snp | G/T | 1.68596e-05 | 0.00290336 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103189 | TGGGGCCTCGGATGG[G/T]GTAGGAAACTGACTC | 81858 |
| rs749957315 | snp | C/T | 5.36155e-05 | 0.00517734 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103257 | TCCAGGCTCAGGGCG[C/T]CCCCCCGCCCTACAT | 81858 |
| rs749975820 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104372 | GACAGACAGGCTCCA[C/T]AACCAGTAGACGTAG | 81858 |
| rs750009163 | snp | C/G | 1.7049e-05 | 0.00291962 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099446 | CTGTGGCCAGAGCAT[C/G]AGGGCAGGTGATGTC | 81858 |
| rs750068285 | snp | C/G | 1.67528e-05 | 0.00289415 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099540 | TGCAACAGTGCAGTG[C/G]GGGTGGACCTGCAGG | 81858 |
| rs750163708 | snp | A/G | 1.66499e-05 | 0.00288525 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105823 | GCCGCGCCCTTCAGT[A/G]GAACCTGGGGGAAGC | 81858 |
| rs750288637 | snp | A/G | 4.99205e-05 | 0.00499578 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105869 | CTCTGCATCCTATAG[A/G]ATTGAGAGCTACTCA | 81858 |
| rs750450161 | snp | C/T | 3.33962e-05 | 0.0040862 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099371 | GCGCTCAGGCACACA[C/T]AGGCACCGTCCGATG | 81858 |
| rs750648890 | snp | A/G | 1.65597e-05 | 0.00287743 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105692 | CAAAGACATGAAGCT[A/G]TTGGAGAACTCGAGC | 81858 |
| rs750766780 | snp | G/T | 5.02871e-05 | 0.00501408 | intron-variant | SHARPIN | GRCh38.p7 | 8:144098997 | AGGACCAGCTGGGCT[G/T]GGGGAAGAGAGACAG | 81858 |
| rs750797394 | snp | C/T | 3.33061e-05 | 0.00408068 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106157 | CTTCTACCTGATTGC[C/T]ACGCTCAATGAGTCC | 81858 |
| rs750960945 | in-del | -/CACCCCACCTCCCA | 1.70825e-05 | 0.00292249 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099237 | AGGACTGTGGGGCTG[-/CACCCCACCTCCCA]CACCCCACCTCCCAC | 81858 |
| rs751015946 | in-del | -/TGGGCT | 1.66663e-05 | 0.00288667 | cds-indel, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103144 | GAGGGTTCCAGGCCC[-/TGGGCT]TCCTGGTGGAGGCTG | 81858 |
| rs751022913 | snp | A/G | 1.67312e-05 | 0.00289229 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098984 | GTGCAGGAAGGACAG[A/G]ACCAGCTGGGCTGGG | 81858 |
| rs751058075 | snp | C/T | 3.33161e-05 | 0.00408129 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106142 | CAGCCGCAAGACCCT[C/T]TTCTACCTGATTGCC | 81858 |
| rs751153793 | snp | C/T | 1.67262e-05 | 0.00289185 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099382 | CACACAGGCACCGTC[C/T]GATGACCCAGCGTTG | 81858 |
| rs751182815 | snp | C/T | 3.32801e-05 | 0.00407908 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103072 | GTCCTTCCACGGTGG[C/T]ACCTCGGACTAGGAC | 81858 |
| rs751329631 | snp | A/C | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098470 | GGGGTCTGGGAAGAG[A/C]TCCCCATGCCATGCT | 81858 |
| rs751476490 | snp | C/T | 1.66463e-05 | 0.00288494 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105817 | CACACTGCCGCGCCC[C/T]TCAGTGGAACCTGGG | 81858 |
| rs751554369 | snp | C/G | 0.000141335 | 0.00840522 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099183 | GTCCATCTTCTGGGG[C/G]TGCTGAGGGCTAGGT | 81858 |
| rs751670932 | snp | C/T | 1.66983e-05 | 0.00288944 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099278 | CATCGAGGACTGACC[C/T]GGGGCTTCTCGAGGA | 81858 |
| rs751816932 | in-del | -/T | 1.80917e-05 | 0.00300758 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100076 | CTTGCTGCCTAGAGG[-/T]TAAGATATGGGTGTG | 81858 |
| rs751867164 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104952 | CTCCTGGGATTTGTA[-/G]TTCCACCGCGGCTTG | 81858 |
| rs751904401 | in-del | -/ACCTCTGGT | 1.77843e-05 | 0.00298191 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098854 | TCCCCTGCCTGTGCC[-/ACCTCTGGT]ACCTCTGGTACCTCT | 81858 |
| rs752077721 | snp | C/G | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098293 | CTGAATGGGAGAAAG[C/G]TGGTACCAATAGGCC | 81858 |
| rs752166347 | snp | C/T | 1.74848e-05 | 0.0029567 | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098869 | CACCTCTGGTACCTC[C/T]GGTGGCTGCTAGGTG | 81858 |
| rs752205365 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100558 | ACCCGCCCTGTGAGG[C/G]CCAGCCCACTGCAAT | 81858 |
| rs752548797 | snp | G/T | 1.69378e-05 | 0.00291009 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099422 | CGGGAAACCGAGCTC[G/T]GAGAACACCTGTGGC | 81858 |
| rs752576178 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101837 | GAGGTTTTGTTCATG[C/T]CAAAGGAGTACCTGG | 81858 |
| rs752653168 | snp | A/C | 1.83673e-05 | 0.0030304 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099915 | ACCCCCCAACCCCCT[A/C]CCCCCACCTGTACCT | 81858 |
| rs752880410 | snp | A/C | 1.68303e-05 | 0.00290084 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099965 | GGCTCCTAGGAAGAT[A/C]TGCCTCAGGTGGAGG | 81858 |
| rs752887435 | snp | A/G | 1.76328e-05 | 0.00296919 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099086 | CCGTGCCCACCTGGA[A/G]TGGACTGGGCAGGCT | 81858 |
| rs752991344 | snp | A/G | 1.8013e-05 | 0.00300103 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103271 | GTCCCCCCGCCCTAC[A/G]TCGCACGAGGAGCAA | 81858 |
| rs753085683 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104587 | CGGTCGGCGGCAGGT[A/C]GGTCGCGAGAGCGGG | 81858 |
| rs753128050 | snp | G/T | 5.25362e-05 | 0.00512497 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103596 | AGCCGGAAGCGCCCA[G/T]GCCGCTCAGGGTCCG | 81858 |
| rs753181517 | snp | A/G | 1.66924e-05 | 0.00288893 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099649 | GGTTCAGGGATGGAT[A/G]GGGGACCTGGGATGG | 81858 |
| rs753222991 | in-del | -/C | 5.36155e-05 | 0.00517734 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103257 | CCAGGCTCAGGGCGT[-/C]CCCCCCGCCCTACAT | 81858 |
| rs753247691 | snp | C/T | 0.000190096 | 0.0097474 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103580 | CGCGCCCAGCAGCTC[C/T]AGCCGGAAGCGCCCA | 81858 |
| rs753300716 | snp | A/G | 1.66871e-05 | 0.00288847 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099617 | CAAGTGTGACCTGCA[A/G]CCTGTGCCAGAATGT | 81858 |
| rs753344440 | snp | A/G | 1.67379e-05 | 0.00289287 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099546 | AGTGCAGTGGGGGTG[A/G]ACCTGCAGGGCAACG | 81858 |
| rs753369810 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102387 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCCAAGT | 81858 |
| rs753452002 | snp | A/G | 1.66322e-05 | 0.00288371 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105884 | GATTGAGAGCTACTC[A/G]TGTAAGATGGCAGGA | 81858 |
| rs753558654 | snp | C/T | 1.7219e-05 | 0.00293414 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100000 | TTGAGTGTGGAGGCT[C/T]CCGGGGGACTGGGCA | 81858 |
| rs753600666 | snp | C/T | 3.32956e-05 | 0.00408004 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106004 | CCCCAGCAGGTGAGC[C/T]ATGGTGGGGCCTACC | 81858 |
| rs753688028 | snp | C/T | 1.80133e-05 | 0.00300105 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100067 | GTGAGTTGCTCTTGC[C/T]GCCTAGAGGTAAGAT | 81858 |
| rs753743524 | snp | C/T | 1.66768e-05 | 0.00288758 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099285 | GACTGACCTGGGGCT[C/T]CTCGAGGAGCTGACA | 81858 |
| rs753775959 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105067 | TGGAGAAACTAGGCA[A/G]TTTTTCCGGGTAGAG | 81858 |
| rs753900511 | snp | C/T | 1.65499e-05 | 0.00287657 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105710 | GGAGAACTCGAGCTT[C/T]GAAGCCATCAACTCA | 81858 |
| rs754028171 | snp | A/G | 3.33111e-05 | 0.00408099 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105811 | GGAGGTCACACTGCC[A/G]CGCCCTTCAGTGGAA | 81858 |
| rs754079359 | snp | G/T | 5.66481e-05 | 0.00532173 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099898 | CTATCTGCTATCCCC[G/T]AACCCCCCAACCCCC | 81858 |
| rs754099101 | snp | C/G | 1.75496e-05 | 0.00296217 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099075 | CCTGCCCAGTCCCGT[C/G]CCCACCTGGAGTGGA | 81858 |
| rs754549387 | snp | C/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105388 | AGGGTCCCCGGTGGT[C/T]TAGTCTAGTCCCAGA | 81858 |
| rs754598020 | snp | G/T | 1.66585e-05 | 0.00288599 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106013 | GTGAGCCATGGTGGG[G/T]CCTACCTGGGGCTGG | 81858 |
| rs754615366 | snp | G/T | 1.6628e-05 | 0.00288335 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105894 | TACTCATGTAAGATG[G/T]CAGGAGACGACAAAC | 81858 |
| rs754674690 | in-del | -/GGCCCGGCGCCC | 0.00175936 | 0.0296072 | cds-indel, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103649 | TGTGCCTCGGCGTCT[-/GGCCCGGCGCCC]GGCCCGGCGCCCAGC | 81858 |
| rs754762848 | snp | C/G | 1.80915e-05 | 0.00300756 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100075 | CTCTTGCTGCCTAGA[C/G]GTAAGATATGGGTGT | 81858 |
| rs754763038 | snp | A/G | 0.00369843 | 0.0428432 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099209 | TAGGTCCTGTGGCTG[A/G]GGGGGTGGAGCTCAG | 81858 |
| rs754812005 | snp | A/G | 3.33339e-05 | 0.00408238 | stop-gained, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099289 | GACCTGGGGCTTCTC[A/G]AGGAGCTGACAGCAA | 81858 |
| rs755007938 | snp | G/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099868 | TAAGGAAAGGACAGC[G/T]GTCACCACTGGGGAC | 81858 |
| rs755155409 | snp | A/G | 0.000117462 | 0.00766273 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099008 | GGCTGGGGGAAGAGA[A/G]ACAGTTGTTGCTTCC | 81858 |
| rs755204398 | snp | C/T | 2.00379e-05 | 0.00316521 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099901 | TCTGCTATCCCCGAA[C/T]CCCCCAACCCCCTCC | 81858 |
| rs755259384 | snp | C/T | 1.75779e-05 | 0.00296457 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099078 | GCCCAGTCCCGTGCC[C/T]ACCTGGAGTGGACTG | 81858 |
| rs755303629 | snp | A/C/G | 3.41304e-05 | 0.00413089 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103207 | AGGAAACTGACTCCA[A/C/G]GGGCCACTCCAAATT | 81858 |
| rs755441109 | snp | A/G | 0.000100232 | 0.00707856 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099561 | GACCTGCAGGGCAAC[A/G]TGTGCAGAGGACGCG | 81858 |
| rs755611511 | in-del | -/CTGGGTCATTC | | | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098802 | CCTGTGGGGGAGGAG[-/CTGGGTCATTC]CTGGGTCATTCCTGT | 81858 |
| rs755680467 | snp | C/G | 1.70845e-05 | 0.00292267 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099451 | GCCAGAGCATCAGGG[C/G]AGGTGATGTCACCTA | 81858 |
| rs755691686 | in-del | -/GAG | 1.66735e-05 | 0.00288729 | cds-indel, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099289 | GACCTGGGGCTTCTC[-/GAG]GAGCTGACAGCAAGT | 81858 |
| rs755733738 | snp | C/G | 1.6752e-05 | 0.00289408 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099541 | GCAACAGTGCAGTGG[C/G]GGTGGACCTGCAGGG | 81858 |
| rs755826356 | snp | C/T | 1.66471e-05 | 0.00288501 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105828 | GCCCTTCAGTGGAAC[C/T]TGGGGGAAGCATGCT | 81858 |
| rs755829381 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101779 | ATTTTATATGTCTGC[C/G]TCCTCCCCTCTAAAA | 81858 |
| rs755875968 | snp | A/C | 1.66416e-05 | 0.00288453 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105870 | TCTGCATCCTATAGG[A/C]TTGAGAGCTACTCAT | 81858 |
| rs756000276 | snp | G/T | 1.70432e-05 | 0.00291913 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099989 | GTGGAGGGCCCTTGA[G/T]TGTGGAGGCTTCCGG | 81858 |
| rs756327262 | snp | A/G | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098512 | TGAGGCTCAGGGTCC[A/G]GGCCCATTCTTCAGT | 81858 |
| rs756359356 | snp | C/T | 1.69461e-05 | 0.0029108 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099825 | TGCAATAGCCCGGGC[C/T]AGGCTCCCTGCCAGC | 81858 |
| rs756502012 | snp | C/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105455 | GCCTGGACTTACCAC[C/T]CTCAGGTAAAACAGG | 81858 |
| rs756529630 | in-del | -/G | 1.67237e-05 | 0.00289164 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103174 | TAGCTCGTGCTGGGT[-/G]GGGGCCTCGGATGGT | 81858 |
| rs756606722 | snp | C/T | 1.66388e-05 | 0.00288429 | stop-gained, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103092 | CGGACTAGGACTGCC[C/T]ACCGCTGAGCTTCCT | 81858 |
| rs756885460 | snp | A/G/T | 8.36497e-05 | 0.00646674 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099383 | ACACAGGCACCGTCC[A/G/T]ATGACCCAGCGTTGC | 81858 |
| rs756925077 | snp | C/G | 1.67094e-05 | 0.0028904 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103172 | CTGTAGCTCGTGCTG[C/G]GTGGGGCCTCGGATG | 81858 |
| rs757103477 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099853 | AGCTCTTCTGCAGGG[C/T]AAGGAAAGGACAGCT | 81858 |
| rs757180289 | snp | C/T | 0.000116545 | 0.00763276 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105819 | CACTGCCGCGCCCTT[C/T]AGTGGAACCTGGGGG | 81858 |
| rs757426535 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098641 | GGGATGCTTGCTGGC[A/T]CTTAAGGGTCTTTAA | 81858 |
| rs757437489 | snp | A/G | 6.67646e-05 | 0.00577736 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099671 | CTGGGATGGTCACGA[A/G]GACAAGGTGAAGAAG | 81858 |
| rs757638960 | snp | C/T | 5.02416e-05 | 0.00501181 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099757 | ACACTCAGGGCCACA[C/T]GATGCTGGGCCAGGA | 81858 |
| rs757765007 | snp | C/T | 3.33183e-05 | 0.00408143 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106148 | CAAGACCCTCTTCTA[C/T]CTGATTGCCACGCTC | 81858 |
| rs757850454 | in-del | -/ACCTCTGGT | 1.77843e-05 | 0.00298191 | intron-variant, cds-indel | SHARPIN | GRCh38.p7 | 8:144098855 | TCCCCTGCCTGTGCC[-/ACCTCTGGT]ACCTCTGGTGGCTGC | 81858 |
| rs757912877 | snp | A/G | 1.70531e-05 | 0.00291997 | missense, nc-transcript-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098891 | TGCTAGGTGGAAGCT[A/G]CAGCAAGGGGGTCCC | 81858 |
| rs757950460 | snp | A/G | 1.66582e-05 | 0.00288597 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106036 | GGGGCTGGGGGTTGA[A/G]GGGAGGTGATGGGCC | 81858 |
| rs758002159 | snp | C/T | 1.66471e-05 | 0.00288501 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103059 | CACTGACCATTCTGT[C/T]CTTCCACGGTGGCAC | 81858 |
| rs758018859 | snp | G/T | 1.8124e-05 | 0.00301026 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100082 | TGCCTAGAGGTAAGA[G/T]ATGGGTGTGCTGTGC | 81858 |
| rs758085288 | snp | C/T | 1.66682e-05 | 0.00288684 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106121 | GGGCCCCCTCAGTGA[C/T]AAGTGCAGCCGCAAG | 81858 |
| rs758407548 | snp | A/G | 1.68519e-05 | 0.0029027 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099972 | AGGAAGATCTGCCTC[A/G]GGTGGAGGGCCCTTG | 81858 |
| rs758600035 | snp | A/C | 1.7748e-05 | 0.00297887 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099174 | AAGTTCCCCGTCCAT[A/C]TTCTGGGGGTGCTGA | 81858 |
| rs758679181 | snp | C/T | 3.61481e-05 | 0.0042512 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103273 | CCCCCCGCCCTACAT[C/T]GCACGAGGAGCAAAG | 81858 |
| rs758734207 | snp | G/T | 5.24123e-05 | 0.00511892 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103597 | GCCGGAAGCGCCCAG[G/T]CCGCTCAGGGTCCGC | 81858 |
| rs758854912 | snp | C/G | 1.66932e-05 | 0.002889 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099658 | ATGGATGGGGGACCT[C/G]GGATGGTCACGAGGA | 81858 |
| rs759019439 | snp | C/T | 1.67156e-05 | 0.00289093 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099743 | CCTCCTGAAGCTGAA[C/T]ACTCAGGGCCACACG | 81858 |
| rs759030326 | snp | A/G | 3.32353e-05 | 0.00407634 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105903 | AAGATGGCAGGAGAC[A/G]ACAAACACATGTTCA | 81858 |
| rs759043093 | snp | A/C | 0.00249687 | 0.0352449 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103750 | CGCCCGCTGGCGGCG[A/C]CATCTCCGGTCCGGC | 81858 |
| rs759264930 | snp | C/T | 0.000252923 | 0.0112427 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099810 | CTTCTCGTCTCCACC[C/T]GCAATAGCCCGGGCC | 81858 |
| rs759369208 | snp | A/G | 1.66668e-05 | 0.00288672 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106107 | GGCGGTGAGGAGGAG[A/G]GCCCCCTCAGTGACA | 81858 |
| rs759422460 | snp | A/G | 1.66707e-05 | 0.00288705 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103153 | CAGGCCCTCCTGGTG[A/G]AGGCTGTAGCTCGTG | 81858 |
| rs759455122 | snp | G/T | 8.34369e-05 | 0.00645844 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099623 | TGACCTGCAGCCTGT[G/T]CCAGAATGTGGGTTC | 81858 |
| rs759498642 | snp | A/G | 1.67075e-05 | 0.00289023 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099373 | GCTCAGGCACACACA[A/G]GCACCGTCCGATGAC | 81858 |
| rs759504344 | snp | C/T | 9.99101e-05 | 0.00706718 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105812 | GAGGTCACACTGCCG[C/T]GCCCTTCAGTGGAAC | 81858 |
| rs759754943 | snp | C/G/T | 4.99308e-05 | 0.00499633 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105856 | GCTTCATGGTTCTCT[C/G/T]TGCATCCTATAGGAT | 81858 |
| rs759831761 | snp | A/G | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098346 | CTGGGGGACCAGGGT[A/G]GACAGTAGGAGACAA | 81858 |
| rs759843484 | snp | C/T | 3.38794e-05 | 0.00411564 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099946 | CTCTCCGTCAAGTTT[C/T]CAGGGCTCCTAGGAA | 81858 |
| rs759968173 | snp | A/G | 0.000196782 | 0.00991726 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099155 | ATGGGGGAAACAAGC[A/G]TCCAAGTTCCCCGTC | 81858 |
| rs760023026 | snp | A/C | 1.67773e-05 | 0.00289626 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099262 | TCCCACACCCCACCC[A/C]CATCGAGGACTGACC | 81858 |
| rs760040462 | snp | C/T | 5.1307e-05 | 0.00506467 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103590 | AGCTCCAGCCGGAAG[C/T]GCCCAGGCCGCTCAG | 81858 |
| rs760223155 | snp | C/G | 1.78624e-05 | 0.00298846 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103260 | AGGCTCAGGGCGTCC[C/G]CCCGCCCTACATCGC | 81858 |
| rs760404820 | snp | G/T | 0.00021077 | 0.0102636 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103697 | CACAGCCAAGAGCAC[G/T]GCGGCGGAGCCCAAG | 81858 |
| rs760435777 | snp | C/T | 1.66996e-05 | 0.00288956 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099596 | ATGCGGCAGAGGCAG[C/T]GTCTTCAAGTGTGAC | 81858 |
| rs760503884 | in-del | -/A | 1.92643e-05 | 0.00310351 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099907 | ATCCCCGAACCCCCC[-/A]ACCCCCTCCCCCCAC | 81858 |
| rs760553615 | snp | A/G | 3.32812e-05 | 0.00407915 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105997 | GACTGAGCCCCAGCA[A/G]GTGAGCCATGGTGGG | 81858 |
| rs760561566 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104056 | GGGGGCGAAGGGTCA[A/G]GGGGCGAAGCACCGG | 81858 |
| rs760606899 | snp | C/G | 0.000249973 | 0.0111769 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106088 | CAGACTCAGCAAAAG[C/G]CAAGGCGGTGAGGAG | 81858 |
| rs760608585 | snp | A/G | 1.77505e-05 | 0.00297908 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100045 | GCTTCTGGGCCCAAG[A/G]CTGGTGGTGAGTTGC | 81858 |
| rs760614885 | in-del | -/A | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101892 | GCTTGGTGAATGACT[-/A]AAAGAGAGCTTAGCT | 81858 |
| rs760934092 | snp | A/C | 3.81862e-05 | 0.0043694 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099896 | GACTATCTGCTATCC[A/C]CGAACCCCCCAACCC | 81858 |
| rs761160185 | snp | C/G/T | 0.000120337 | 0.00775606 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099936 | ACCTGTACCTCTCTC[C/G/T]GTCAAGTTTCCAGGG | 81858 |
| rs761225236 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104215 | CCTTCGCCCGCAGAC[A/C]CCAGCCCCCGCCACG | 81858 |
| rs761254735 | snp | A/C | 1.74175e-05 | 0.00295101 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099064 | TCCTGGCCCTCCCTG[A/C]CCAGTCCCGTGCCCA | 81858 |
| rs761265219 | snp | A/G | 1.79287e-05 | 0.002994 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099139 | GGGGGTAGCCCCAAT[A/G]ATGGGGGAAACAAGC | 81858 |
| rs761379275 | snp | C/G | 1.79303e-05 | 0.00299413 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099128 | GCTGGGGGCCTGGGG[C/G]TAGCCCCAATGATGG | 81858 |
| rs761552907 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105101 | AGGAACCTGTAGTTT[G/T]CCTCTCCCCGGGCCA | 81858 |
| rs761564851 | snp | A/G | 1.77436e-05 | 0.0029785 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103253 | AGAGTCCAGGCTCAG[A/G]GCGTCCCCCCGCCCT | 81858 |
| rs761689468 | snp | G/T | 1.67638e-05 | 0.0028951 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099537 | AGCTGCAACAGTGCA[G/T]TGGGGGTGGACCTGC | 81858 |
| rs761738333 | snp | C/G | 1.67139e-05 | 0.00289079 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099585 | GGACGCGGCGGATGC[C/G]GCAGAGGCAGCGTCT | 81858 |
| rs761788052 | snp | C/G | | | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105831 | CTTCAGTGGAACCTG[C/G]GGGAAGCATGCTTCA | 81858 |
| rs761863965 | snp | A/G | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103018 | GGCCAAGGCTATTCC[A/G]AATTGTAATTGTATC | 81858 |
| rs762075429 | snp | A/G | 3.31439e-05 | 0.00407073 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105679 | GGAGCTCCTTCCCCA[A/G]AGACATGAAGCTATT | 81858 |
| rs762132275 | snp | A/G | 1.69035e-05 | 0.00290714 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099816 | GTCTCCACCTGCAAT[A/G]GCCCGGGCCAGGCTC | 81858 |
| rs762173877 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100726 | CTGAACCTCAAGGAT[C/T]ACTTATACATGCTCA | 81858 |
| rs762333513 | in-del | -/G | 1.8136e-05 | 0.00301126 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100084 | CTAGAGGTAAGATAT[-/G]GGGTGTGCTGTGCTG | 81858 |
| rs762338240 | snp | C/T | 1.67405e-05 | 0.00289309 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098991 | AAGGACAGGACCAGC[C/T]GGGCTGGGGGAAGAG | 81858 |
| rs762410517 | snp | A/G | 1.67237e-05 | 0.00289164 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098979 | TGAAGGTGCAGGAAG[A/G]ACAGGACCAGCTGGG | 81858 |
| rs762440714 | snp | A/C/G/T | 0.000185797 | 0.00963689 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099815 | CGTCTCCACCTGCAA[A/C/G/T]AGCCCGGGCCAGGCT | 81858 |
| rs762617492 | snp | C/T | 1.72624e-05 | 0.00293784 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099052 | TGCCCATGGCTGTCC[C/T]GGCCCTCCCTGCCCA | 81858 |
| rs762708580 | snp | A/G | 1.76543e-05 | 0.002971 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103246 | AAGAGGGAGAGTCCA[A/G]GCTCAGGGCGTCCCC | 81858 |
| rs762829612 | snp | C/G | 1.69175e-05 | 0.00290834 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099513 | CCCTGTGCCCACCTG[C/G]TCCTGGAGAGCTGCA | 81858 |
| rs762859512 | snp | A/G | 6.77599e-05 | 0.00582025 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099423 | GGGAAACCGAGCTCT[A/G]AGAACACCTGTGGCC | 81858 |
| rs763020536 | snp | C/T | 1.66037e-05 | 0.00288125 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105971 | GGCACTTTCTCCACC[C/T]CAGACTTCAGGACTG | 81858 |
| rs763118369 | snp | A/G | 1.67629e-05 | 0.00289503 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103004 | AACCAGGACTGGGGG[A/G]CCAAGGCTATTCCAA | 81858 |
| rs763145216 | snp | G/T | 1.76204e-05 | 0.00296814 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100032 | GGAGACAGGGCATGC[G/T]TCTGGGCCCAAGGCT | 81858 |
| rs763238024 | in-del | -/GTGTGGAG | 5.10964e-05 | 0.00505427 | frameshift-variant, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099989 | GTGGAGGGCCCTTGA[-/GTGTGGAG]GCTTCCGGGGGACTG | 81858 |
| rs763403179 | snp | C/T | 0.000178492 | 0.00944532 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103777 | CGGCCGGGTCCCACC[C/T]CTCCGAGCGCGCTTC | 81858 |
| rs763456336 | snp | A/G | 1.67332e-05 | 0.00289246 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099751 | AGCTGAACACTCAGG[A/G]CCACACGATGCTGGG | 81858 |
| rs763558700 | snp | G/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101952 | TCTCTTACATCACTG[G/T]CTGGCTGTCTTCCTA | 81858 |
| rs763574934 | snp | A/G | 1.67312e-05 | 0.00289229 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098983 | GGTGCAGGAAGGACA[A/G]GACCAGCTGGGCTGG | 81858 |
| rs763703723 | snp | A/T | 1.66582e-05 | 0.00288597 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106137 | AAGTGCAGCCGCAAG[A/T]CCCTCTTCTACCTGA | 81858 |
| rs763821563 | snp | C/G | 1.69456e-05 | 0.00291075 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099425 | GAAACCGAGCTCTGA[C/G]AACACCTGTGGCCAG | 81858 |
| rs763825144 | snp | A/G | 1.66405e-05 | 0.00288443 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103070 | CTGTCCTTCCACGGT[A/G]GCACCTCGGACTAGG | 81858 |
| rs763997537 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104146 | CCAGCGTGCGACTAT[C/T]CCAGCGCCTAACGGC | 81858 |
| rs764006979 | snp | A/G | 1.76636e-05 | 0.00297178 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103247 | AGAGGGAGAGTCCAG[A/G]CTCAGGGCGTCCCCC | 81858 |
| rs764026759 | snp | C/T | 1.6888e-05 | 0.00290581 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099516 | TGTGCCCACCTGCTC[C/T]TGGAGAGCTGCAACA | 81858 |
| rs764107324 | snp | A/C/G | 0.00012416 | 0.00787818 | synonymous-codon, missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100043 | ATGCTTCTGGGCCCA[A/C/G]GGCTGGTGGTGAGTT | 81858 |
| rs764157250 | snp | C/T | 1.66996e-05 | 0.00288956 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099277 | CCATCGAGGACTGAC[C/T]TGGGGCTTCTCGAGG | 81858 |
| rs764258695 | snp | C/T | 8.86658e-05 | 0.00665771 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099177 | TTCCCCGTCCATCTT[C/T]TGGGGGTGCTGAGGG | 81858 |
| rs764352218 | in-del | -/AG | 8.75672e-05 | 0.00661634 | frameshift-variant, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100023 | ACTGGGCAGGGAGAC[-/AG]GGCATGCTTCTGGGC | 81858 |
| rs764455366 | snp | C/T | 1.65767e-05 | 0.00287891 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105676 | CACGGAGCTCCTTCC[C/T]CAAAGACATGAAGCT | 81858 |
| rs764531588 | snp | A/C | 3.34638e-05 | 0.00409033 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099752 | GCTGAACACTCAGGG[A/C]CACACGATGCTGGGC | 81858 |
| rs764547124 | in-del | -/CCC | 1.65496e-05 | 0.00287655 | intron-variant, cds-indel | SHARPIN | GRCh38.p7 | 8:144098831 | GTGGATTCTGCCCTG[-/CCC]CCCACCTCCCCTGCC | 81858 |
| rs764549165 | snp | A/C | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100548 | TCACCTTCTTACCCG[A/C]CCTGTGAGGCCCAGC | 81858 |
| rs764553309 | snp | C/T | 4.99014e-05 | 0.00499482 | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105634 | GTCTGGTCTCTCACT[C/T]CCCAGGCAATACTAG | 81858 |
| rs764610896 | snp | C/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105523 | CTCCTGATGTGCAGC[C/T]TGGACAGAGGCCAGA | 81858 |
| rs764837171 | snp | A/G | 3.33267e-05 | 0.00408194 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106116 | GAGGAGGGCCCCCTC[A/G]GTGACAAGTGCAGCC | 81858 |
| rs764859723 | snp | A/G | 5.01685e-05 | 0.00500817 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098975 | TTGATGAAGGTGCAG[A/G]AAGGACAGGACCAGC | 81858 |
| rs764880938 | snp | A/G | 5.2796e-05 | 0.00513763 | splice-donor-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098864 | TGTGCCACCTCTGGT[A/G]CCTCTGGTGGCTGCT | 81858 |
| rs764927919 | snp | C/T | 1.66632e-05 | 0.0028864 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106018 | CCATGGTGGGGCCTA[C/T]CTGGGGCTGGGGGTT | 81858 |
| rs764962159 | snp | C/G | 6.66822e-05 | 0.00577379 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103044 | GTATCCATTACAGGG[C/G]ACTGACCATTCTGTC | 81858 |
| rs764984315 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105984 | CCCCAGACTTCAGGA[C/T]TGAGCCCCAGCAGGT | 81858 |
| rs765037666 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105102 | GGAACCTGTAGTTTT[C/T]CTCTCCCCGGGCCAG | 81858 |
| rs765165425 | snp | C/G | 1.66757e-05 | 0.00288749 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103156 | GCCCTCCTGGTGGAG[C/G]CTGTAGCTCGTGCTG | 81858 |
| rs765227799 | snp | C/T | 1.69292e-05 | 0.00290935 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099419 | TGGCGGGAAACCGAG[C/T]TCTGAGAACACCTGT | 81858 |
| rs765378567 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100775 | GCTTCCTTGGTCACA[C/T]GGTTCATGCCATGAC | 81858 |
| rs765674423 | snp | A/G | 3.34818e-05 | 0.00409143 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099267 | CACCCCACCCCCATC[A/G]AGGACTGACCTGGGG | 81858 |
| rs765720798 | snp | A/T | 5.20291e-05 | 0.00510018 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103595 | CAGCCGGAAGCGCCC[A/T]GGCCGCTCAGGGTCC | 81858 |
| rs765773837 | snp | C/T | 0.000918695 | 0.0214127 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103755 | GCTGGCGGCGCCATC[C/T]CCGGTCCGGCCGGGT | 81858 |
| rs765934841 | snp | G/T | 0.000190458 | 0.00975668 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103576 | GTCCCGCGCCCAGCA[G/T]CTCCAGCCGGAAGCG | 81858 |
| rs766116574 | snp | A/G | 1.66427e-05 | 0.00288462 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106000 | TGAGCCCCAGCAGGT[A/G]AGCCATGGTGGGGCC | 81858 |
| rs766243804 | snp | C/T | 1.7872e-05 | 0.00298926 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098849 | CCCACCTCCCCTGCC[C/T]GTGCCACCTCTGGTA | 81858 |
| rs766279310 | snp | C/T | 1.66687e-05 | 0.00288688 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106094 | CAGCAAAAGCCAAGG[C/T]GGTGAGGAGGAGGGC | 81858 |
| rs766369803 | snp | C/T | 1.67307e-05 | 0.00289224 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103021 | CAAGGCTATTCCAAA[C/T]TGTAATTGTATCCAT | 81858 |
| rs766514476 | snp | A/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103433 | CACGGACGAGAAAAC[A/T]GAAGCAAAGAAACAT | 81858 |
| rs766596518 | snp | C/T | 1.65518e-05 | 0.00287674 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105708 | TTGGAGAACTCGAGC[C/T]TTGAAGCCATCAACT | 81858 |
| rs766649934 | snp | C/T | 9.99068e-05 | 0.00706706 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105810 | CGGAGGTCACACTGC[C/T]GCGCCCTTCAGTGGA | 81858 |
| rs766741220 | snp | A/G | 0.000105396 | 0.00725858 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099073 | TCCCTGCCCAGTCCC[A/G]TGCCCACCTGGAGTG | 81858 |
| rs766753036 | snp | C/T | 1.79351e-05 | 0.00299454 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099141 | GGGTAGCCCCAATGA[C/T]GGGGGAAACAAGCGT | 81858 |
| rs767217219 | snp | C/G | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103256 | GTCCAGGCTCAGGGC[C/G]TCCCCCCGCCCTACA | 81858 |
| rs767343694 | snp | C/G | 1.67567e-05 | 0.00289449 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099539 | CTGCAACAGTGCAGT[C/G]GGGGTGGACCTGCAG | 81858 |
| rs767432912 | snp | A/G | 1.6641e-05 | 0.00288448 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105865 | TTCTCTCTGCATCCT[A/G]TAGGATTGAGAGCTA | 81858 |
| rs767486499 | snp | C/T | 1.66125e-05 | 0.00288201 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105985 | CCCAGACTTCAGGAC[C/T]GAGCCCCAGCAGGTG | 81858 |
| rs767534363 | snp | A/G | 1.69352e-05 | 0.00290987 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099979 | TCTGCCTCAGGTGGA[A/G]GGCCCTTGAGTGTGG | 81858 |
| rs767558066 | snp | A/G | 1.66743e-05 | 0.00288736 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099363 | GCAAGGCTGCGCTCA[A/G]GCACACACAGGCACC | 81858 |
| rs767841730 | snp | C/G | 1.77593e-05 | 0.00297982 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099887 | ACCACTGGGGACTAT[C/G]TGCTATCCCCGAACC | 81858 |
| rs767942814 | snp | C/T | 1.67579e-05 | 0.00289459 | splice-acceptor-variant | SHARPIN | GRCh38.p7 | 8:144098996 | CAGGACCAGCTGGGC[C/T]GGGGGAAGAGAGACA | 81858 |
| rs767943795 | snp | C/T | 6.7651e-05 | 0.00581558 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099820 | CCACCTGCAATAGCC[C/T]GGGCCAGGCTCCCTG | 81858 |
| rs767961720 | in-del | -/AATTGT | 1.67354e-05 | 0.00289265 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103019 | GCCAAGGCTATTCCA[-/AATTGT]AATTGTATCCATTAC | 81858 |
| rs768025678 | snp | A/G | 1.66454e-05 | 0.00288486 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105833 | TCAGTGGAACCTGGG[A/G]GAAGCATGCTTCATG | 81858 |
| rs768069353 | snp | C/T | 1.7505e-05 | 0.00295841 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099071 | CCTCCCTGCCCAGTC[C/T]CGTGCCCACCTGGAG | 81858 |
| rs768130430 | snp | C/T | 1.72719e-05 | 0.00293865 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099871 | GGAAAGGACAGCTGT[C/T]ACCACTGGGGACTAT | 81858 |
| rs768154841 | in-del | -/CGCGGCGGATGCGGCAGAGGC | 3.33895e-05 | 0.00408579 | cds-indel, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099572 | AACGTGTGCAGAGGA[-/CGCGGCGGATGCGGCAGAGGC]CGCGGCGGATGCGGC | 81858 |
| rs768255196 | snp | G/T | 5.35633e-05 | 0.00517482 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099924 | CCCCCTCCCCCCACC[G/T]GTACCTCTCTCCGTC | 81858 |
| rs768255562 | snp | A/G | 3.45095e-05 | 0.00415374 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099053 | GCCCATGGCTGTCCT[A/G]GCCCTCCCTGCCCAG | 81858 |
| rs768308625 | snp | A/C | 1.79133e-05 | 0.00299271 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099122 | CAGCTGGCTGGGGGC[A/C]TGGGGGTAGCCCCAA | 81858 |
| rs768507571 | snp | A/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105346 | GAATGTTGAGCAACA[A/T]TCTCAGCCAGCAGCC | 81858 |
| rs768651874 | snp | C/T | 3.62549e-05 | 0.00425748 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103539 | CTGACCGCGCGCCCT[C/T]CGCCCCCACTCACCG | 81858 |
| rs768768411 | snp | A/T | 0.000190894 | 0.00976784 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103620 | GGGTCCGCGCTCAGC[A/T]GCAGCCTCCGCAGCT | 81858 |
| rs768870232 | snp | A/G | 3.36372e-05 | 0.00410091 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099401 | GACCCAGCGTTGCAC[A/G]GCTGGCGGGAAACCG | 81858 |
| rs769106513 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099467 | AGGTGATGTCACCTA[A/G]GCTCCTCTGCCCCTG | 81858 |
| rs769153681 | snp | C/T | 1.70854e-05 | 0.00292274 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099470 | TGATGTCACCTAGGC[C/T]CCTCTGCCCCTGGCA | 81858 |
| rs769276287 | snp | A/G | 4.9884e-05 | 0.00499395 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105785 | AGGCAGGCTGGGGGG[A/G]CTGGCATCTCGGAGG | 81858 |
| rs769318482 | snp | A/C | 1.65913e-05 | 0.00288017 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105666 | CCCTCTGGAGCACGG[A/C]GCTCCTTCCCCAAAG | 81858 |
| rs769327322 | snp | A/C | | | downstream-variant-500B | SHARPIN | GRCh38.p7 | 8:144098200 | CTAGGAAGGGAAGGA[A/C]AACACCCATTTTCAT | 81858 |
| rs769479344 | in-del | -/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101602 | TTTTTTTTTTTTTAG[-/T]AGTCAGGGTTTCACC | 81858 |
| rs769498586 | snp | A/T | 1.71953e-05 | 0.00293212 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099863 | CAGGGTAAGGAAAGG[A/T]CAGCTGTCACCACTG | 81858 |
| rs769601165 | snp | C/G/T | 0.000207152 | 0.0101752 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099051 | ATGCCCATGGCTGTC[C/G/T]TGGCCCTCCCTGCCC | 81858 |
| rs769686381 | snp | A/G | 5.24801e-05 | 0.00512224 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103236 | TTAACCTGAGAAGAG[A/G]GAGAGTCCAGGCTCA | 81858 |
| rs769935596 | in-del | -/C | 1.89224e-05 | 0.00307585 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099909 | CCCCGAACCCCCCAA[-/C]CCCCTCCCCCCACCT | 81858 |
| rs770003038 | snp | A/G | 1.66048e-05 | 0.00288134 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105948 | GAGGGCCAGCCCCAC[A/G]TGCTGGAGGCACTTT | 81858 |
| rs770036763 | snp | C/G | 3.63894e-05 | 0.00426537 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100111 | GCTGTGGCCTCTGTC[C/G]AGGCCTCTAGGCCCT | 81858 |
| rs770199747 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103340 | CCTAAGCCCTGTACG[C/T]CTATCATCAAATCCT | 81858 |
| rs770287630 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104320 | GGCCACGGCCAATGA[A/G]CGCCGGGGGTAAGCG | 81858 |
| rs770319429 | snp | C/T | 8.31525e-05 | 0.00644743 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099322 | AGAGGAAAGCAGGGT[C/T]CCCATCCTGCCGAAC | 81858 |
| rs770382059 | snp | C/T | | | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100066 | GGTGAGTTGCTCTTG[C/T]TGCCTAGAGGTAAGA | 81858 |
| rs770546108 | snp | G/T | 0.000150294 | 0.00866744 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099727 | CCAGGTGGGAAGCAG[G/T]CCTCCTGAAGCTGAA | 81858 |
| rs770685421 | snp | A/G | 3.31978e-05 | 0.00407404 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105659 | TACTAGCCCCTCTGG[A/G]GCACGGAGCTCCTTC | 81858 |
| rs770739038 | snp | C/T | 1.68332e-05 | 0.00290109 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099805 | GCCCCCTTCTCGTCT[C/T]CACCTGCAATAGCCC | 81858 |
| rs770838568 | snp | A/G | 1.66123e-05 | 0.00288199 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106222 | GCCATGAGTTCAGCC[A/G]GGAGCCCAGCCTTAG | 81858 |
| rs770955793 | snp | C/T | 3.34415e-05 | 0.00408896 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098958 | CAGGGCGGTCTGGGG[C/T]ATTGATGAAGGTGCA | 81858 |
| rs771009347 | snp | C/T | 3.37262e-05 | 0.00410633 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099028 | TTGTTGCTTCCCTGC[C/T]CTTTCCAATGCCCAT | 81858 |
| rs771022710 | snp | A/C | 0.000194534 | 0.00986047 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103533 | AGAGGACTGACCGCG[A/C]GCCCTCCGCCCCCAC | 81858 |
| rs771239652 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105667 | CCTCTGGAGCACGGA[A/G]CTCCTTCCCCAAAGA | 81858 |
| rs771446311 | snp | C/T | 1.66054e-05 | 0.00288139 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105938 | GTTCTGCCAGGAGGG[C/T]CAGCCCCACGTGCTG | 81858 |
| rs771449782 | snp | A/G | 8.63804e-05 | 0.00657136 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100005 | TGTGGAGGCTTCCGG[A/G]GGACTGGGCAGGGAG | 81858 |
| rs771499771 | snp | A/C | 1.73537e-05 | 0.0029456 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100009 | GAGGCTTCCGGGGGA[A/C]TGGGCAGGGAGACAG | 81858 |
| rs771529759 | snp | C/T | 3.36496e-05 | 0.00410167 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099257 | CCACCTCCCACACCC[C/T]ACCCCCATCGAGGAC | 81858 |
| rs771572333 | snp | A/G | 0.000104132 | 0.00721494 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099216 | TGTGGCTGAGGGGGT[A/G]GAGCTCAGGACTGTG | 81858 |
| rs771611655 | snp | A/G | 1.66935e-05 | 0.00288903 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103035 | ATTGTAATTGTATCC[A/G]TTACAGGGCACTGAC | 81858 |
| rs771624288 | snp | A/G | 1.81741e-05 | 0.00301441 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100094 | AGATATGGGTGTGCT[A/G]TGCTGTGGCCTCTGT | 81858 |
| rs771845419 | in-del | -/C | 1.83567e-05 | 0.00302952 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099894 | GGGACTATCTGCTAT[-/C]CCCGAACCCCCCAAC | 81858 |
| rs771898974 | in-del | -/T | 3.32662e-05 | 0.00407824 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105791 | CTGGGGGGGCTGGCA[-/T]TCTCGGAGGTCACAC | 81858 |
| rs771912667 | snp | C/T | 0.000381461 | 0.0138053 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103545 | GCGCGCCCTCCGCCC[C/T]CACTCACCGCCCCAG | 81858 |
| rs771915675 | snp | C/T | 1.80713e-05 | 0.00300588 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098834 | GATTCTGCCCTGCCC[C/T]CCACCTCCCCTGCCT | 81858 |
| rs772090523 | snp | A/C | 3.33784e-05 | 0.0040851 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099688 | ACAAGGTGAAGAAGC[A/C]GCCCCAGGCCTCACC | 81858 |
| rs772117369 | snp | A/G | 1.66524e-05 | 0.00288547 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103126 | GGTTGAGGAAGTGCA[A/G]GCTGAGGGTTCCAGG | 81858 |
| rs772156416 | snp | C/T | 5.80984e-05 | 0.00538942 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099902 | CTGCTATCCCCGAAC[C/T]CCCCAACCCCCTCCC | 81858 |
| rs772240216 | snp | A/C | 1.72454e-05 | 0.00293639 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103219 | CCAGGGGCCACTCCA[A/C]ATTAACCTGAGAAGA | 81858 |
| rs772365786 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105117 | CCTCTCCCCGGGCCA[A/G]AAAGTAGCCAAAACG | 81858 |
| rs772638818 | snp | A/G | 1.66446e-05 | 0.00288479 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105848 | GGAAGCATGCTTCAT[A/G]GTTCTCTCTGCATCC | 81858 |
| rs772694137 | snp | C/T | 1.74921e-05 | 0.00295732 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099929 | TCCCCCCACCTGTAC[C/T]TCTCTCCGTCAAGTT | 81858 |
| rs772800601 | snp | A/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105553 | ACTCAGCTTGTTCCT[A/G]GCGGCTCCACTTAGT | 81858 |
| rs772832418 | snp | A/G | 5.5107e-05 | 0.00524886 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103691 | GGCGTGCACAGCCAA[A/G]AGCACTGCGGCGGAG | 81858 |
| rs773106949 | snp | C/T | 3.32369e-05 | 0.00407644 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105989 | GACTTCAGGACTGAG[C/T]CCCAGCAGGTGAGCC | 81858 |
| rs773124678 | snp | C/T | 6.66556e-05 | 0.00577264 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106068 | AGCTGATGGTTCTGT[C/T]TGTGCAGACTCAGCA | 81858 |
| rs773204855 | in-del | -/C | 2.04463e-05 | 0.0031973 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099900 | TCTGCTATCCCCGAA[-/C]CCCCCCAACCCCCTC | 81858 |
| rs773225447 | snp | A/G | 1.66671e-05 | 0.00288674 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103150 | TTCCAGGCCCTCCTG[A/G]TGGAGGCTGTAGCTC | 81858 |
| rs773265225 | snp | A/T | 1.80941e-05 | 0.00300778 | intron-variant, utr-variant-3-prime | SHARPIN | GRCh38.p7 | 8:144098837 | TCTGCCCTGCCCCCC[A/T]CCTCCCCTGCCTGTG | 81858 |
| rs773282336 | snp | C/T | 3.38158e-05 | 0.00411178 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099415 | CGGCTGGCGGGAAAC[C/T]GAGCTCTGAGAACAC | 81858 |
| rs773294814 | snp | A/G | 3.48517e-05 | 0.00417428 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103233 | AAATTAACCTGAGAA[A/G]AGGGAGAGTCCAGGC | 81858 |
| rs773320403 | snp | C/G | 1.67279e-05 | 0.002892 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098950 | CTCACAGCCAGGGCG[C/G]TCTGGGGCATTGATG | 81858 |
| rs773581978 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103400 | AGGTCCCAGTAGGTC[C/T]GAGCGTCACCCCCAT | 81858 |
| rs773586773 | snp | C/T | 1.72662e-05 | 0.00293817 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099934 | CCACCTGTACCTCTC[C/T]CCGTCAAGTTTCCAG | 81858 |
| rs773640004 | snp | C/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144099893 | GGGGACTATCTGCTA[C/T]CCCCGAACCCCCCAA | 81858 |
| rs773682714 | snp | A/G | 1.73972e-05 | 0.00294929 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099881 | GCTGTCACCACTGGG[A/G]ACTATCTGCTATCCC | 81858 |
| rs773723143 | snp | C/G | 4.99205e-05 | 0.00499578 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105849 | GAAGCATGCTTCATG[C/G]TTCTCTCTGCATCCT | 81858 |
| rs773888306 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100080 | GCTGCCTAGAGGTAA[A/G]ATATGGGTGTGCTGT | 81858 |
| rs773979958 | snp | A/G | 1.793e-05 | 0.00299411 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099125 | CTGGCTGGGGGCCTG[A/G]GGGTAGCCCCAATGA | 81858 |
| rs774032019 | snp | C/T | 1.67798e-05 | 0.00289648 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099533 | GGAGAGCTGCAACAG[C/T]GCAGTGGGGGTGGAC | 81858 |
| rs774305358 | snp | A/C | 7.34673e-05 | 0.00606038 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103540 | TGACCGCGCGCCCTC[A/C]GCCCCCACTCACCGC | 81858 |
| rs774370156 | snp | C/G | 3.33333e-05 | 0.00408235 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106087 | GCAGACTCAGCAAAA[C/G]CCAAGGCGGTGAGGA | 81858 |
| rs774420523 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103736 | CGCCGCCGCCGCCCC[A/G]CCCGCTGGCGGCGCC | 81858 |
| rs774423254 | snp | A/T | 3.34818e-05 | 0.00409143 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103014 | GGGGGGCCAAGGCTA[A/T]TCCAAATTGTAATTG | 81858 |
| rs774430882 | snp | A/G | 1.66538e-05 | 0.00288559 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099358 | AAGAGGCAAGGCTGC[A/G]CTCAGGCACACACAG | 81858 |
| rs774447183 | snp | C/T | 1.65438e-05 | 0.00287605 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105729 | GCCATCAACTCACAG[C/T]TGACTGTGGAGACTG | 81858 |
| rs774549186 | snp | A/G | 1.66463e-05 | 0.00288494 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103118 | TTCCTGAGGGTTGAG[A/G]AAGTGCAGGCTGAGG | 81858 |
| rs774670680 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101300 | GGAGTGCAGTGGCAC[A/G]ATCACAGCTCACTGC | 81858 |
| rs774802799 | snp | C/T | | | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099325 | GGAAAGCAGGGTCCC[C/T]ATCCTGCCGAACCCC | 81858 |
| rs774943933 | snp | G/T | 3.31653e-05 | 0.00407204 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105673 | GAGCACGGAGCTCCT[G/T]CCCCAAAGACATGAA | 81858 |
| rs775123568 | snp | C/T | 1.7249e-05 | 0.0029367 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099867 | GTAAGGAAAGGACAG[C/T]TGTCACCACTGGGGA | 81858 |
| rs775204088 | snp | A/G | 1.67239e-05 | 0.00289166 | missense, nc-transcript-variant, synonymous-codon | SHARPIN | GRCh38.p7 | 8:144098978 | ATGAAGGTGCAGGAA[A/G]GACAGGACCAGCTGG | 81858 |
| rs775299885 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144104040 | GTTAGAGCTGGTCTT[C/T]GGGGGCGAAGGGTCA | 81858 |
| rs775389013 | in-del | -/C | 0.000112626 | 0.00750337 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099915 | ACCCCCCAACCCCCT[-/C]CCCCCACCTGTACCT | 81858 |
| rs775468027 | snp | C/T | 1.75974e-05 | 0.00296621 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103243 | GAGAAGAGGGAGAGT[C/T]CAGGCTCAGGGCGTC | 81858 |
| rs775537225 | snp | C/T | 0.000103473 | 0.00719207 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100002 | GAGTGTGGAGGCTTC[C/T]GGGGGACTGGGCAGG | 81858 |
| rs775548323 | snp | A/G | 7.00783e-05 | 0.00591897 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144100024 | CTGGGCAGGGAGACA[A/G]GGCATGCTTCTGGGC | 81858 |
| rs775739228 | in-del | -/AGT | | | upstream-variant-2KB, intron-variant, cds-indel | SHARPIN, MAF1 | GRCh38.p7 | 8:144105120 | CTCCCCGGGCCAGAA[-/AGT]AGCCAAAACGAAAGA | 81858 |
| rs775877099 | snp | G/T | 5.02812e-05 | 0.00501379 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103003 | CAACCAGGACTGGGG[G/T]GCCAAGGCTATTCCA | 81858 |
| rs775949388 | snp | A/C | 1.67326e-05 | 0.00289241 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099268 | ACCCCACCCCCATCG[A/C]GGACTGACCTGGGGC | 81858 |
| rs775956036 | snp | C/T | 0.000711111 | 0.0188428 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103776 | CCGGCCGGGTCCCAC[C/T]CCTCCGAGCGCGCTT | 81858 |
| rs776004451 | snp | C/T | 1.66288e-05 | 0.00288343 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099340 | CATCCTGCCGAACCC[C/T]GTAAGAGGCAAGGCT | 81858 |
| rs776073288 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100300 | ATATTTGGGAATTAG[A/G]GCCTTTTCAAACCCT | 81858 |
| rs776345138 | snp | A/G | 3.33289e-05 | 0.00408207 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106103 | CCAAGGCGGTGAGGA[A/G]GAGGGCCCCCTCAGT | 81858 |
| rs776502638 | snp | A/G | 1.66346e-05 | 0.00288393 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105796 | GGGGGCTGGCATCTC[A/G]GAGGTCACACTGCCG | 81858 |
| rs776538261 | snp | C/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105424 | CGTGTTCTGCAGGGG[C/G]TATGGCTGACCTGGA | 81858 |
| rs776696108 | snp | C/T | 1.66441e-05 | 0.00288474 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105854 | ATGCTTCATGGTTCT[C/T]TCTGCATCCTATAGG | 81858 |
| rs776727779 | snp | C/T | 1.70513e-05 | 0.00291982 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099498 | GCAGGGCTCCCCAGA[C/T]CCTGTGCCCACCTGC | 81858 |
| rs776942448 | snp | C/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100711 | CGGCCCCGGCCCCCA[C/G]TGAACCTCAAGGATC | 81858 |
| rs776988893 | snp | A/C/G | 8.37074e-05 | 0.006469 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099758 | CACTCAGGGCCACAC[A/C/G]ATGCTGGGCCAGGAC | 81858 |
| rs777016306 | snp | C/G | 1.6604e-05 | 0.00288127 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105944 | CCAGGAGGGCCAGCC[C/G]CACGTGCTGGAGGCA | 81858 |
| rs777097807 | snp | C/T | 1.69726e-05 | 0.00291308 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099943 | CCTCTCTCCGTCAAG[C/T]TTCCAGGGCTCCTAG | 81858 |
| rs777177495 | snp | C/T | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103321 | TATAGACCATTTACA[C/T]GGTCCTAAGCCCTGT | 81858 |
| rs777277438 | snp | C/G | 1.67922e-05 | 0.00289755 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099260 | CCTCCCACACCCCAC[C/G]CCCATCGAGGACTGA | 81858 |
| rs777280886 | snp | C/G | 1.66341e-05 | 0.00288388 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099315 | AGCAAGTAGAGGAAA[C/G]CAGGGTCCCCATCCT | 81858 |
| rs777326803 | snp | C/T | 1.66305e-05 | 0.00288357 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099323 | GAGGAAAGCAGGGTC[C/T]CCATCCTGCCGAACC | 81858 |
| rs777369922 | snp | A/G | 1.66613e-05 | 0.00288623 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106045 | GGTTGAGGGGAGGTG[A/G]TGGGCCCAGCTGATG | 81858 |
| rs777492504 | in-del | -/G | 1.66696e-05 | 0.00288696 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106027 | GGCCTACCTGGGGCT[-/G]GGGGTTGAGGGGAGG | 81858 |
| rs777628570 | snp | A/C | 1.66073e-05 | 0.00288156 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105653 | AGGCAATACTAGCCC[A/C]TCTGGAGCACGGAGC | 81858 |
| rs777649112 | snp | A/G | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144102187 | GTGAGTTAGGGTCAC[A/G]CTACTGCACTCCAGT | 81858 |
| rs777839426 | snp | C/T | 1.68213e-05 | 0.00290006 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099800 | GGGCTGCCCCCTTCT[C/T]GTCTCCACCTGCAAT | 81858 |
| rs777908449 | snp | A/C | 5.25624e-05 | 0.00512625 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103599 | CGGAAGCGCCCAGGC[A/C]GCTCAGGGTCCGCGC | 81858 |
| rs778021240 | snp | C/T | 1.66977e-05 | 0.00288939 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099573 | AACGTGTGCAGAGGA[C/T]GCGGCGGATGCGGCA | 81858 |
| rs778287529 | snp | A/G | 4.98616e-05 | 0.00499283 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105899 | ATGTAAGATGGCAGG[A/G]GACGACAAACACATG | 81858 |
| rs778333448 | snp | C/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105626 | TACCCATGGTCTGGT[C/G]TCTCACTCCCCAGGC | 81858 |
| rs778378673 | snp | A/G | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102599 | CTTCTAAGCATCTCT[A/G]GAAACATCCTTCTCC | 81858 |
| rs778401532 | snp | A/C | | | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144102636 | CTATCTGCACCAACC[A/C]TTGCCACTGCAGAAC | 81858 |
| rs778417144 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144104824 | AGCCCAGCCAGACCC[A/G]GCCCGGCGCGGCCTG | 81858 |
| rs778435024 | snp | A/C | 1.66454e-05 | 0.00288486 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105836 | GTGGAACCTGGGGGA[A/C]GCATGCTTCATGGTT | 81858 |
| rs778483790 | in-del | -/T | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144101242 | ATTTTATTATTTTTG[-/T]TTTTTTTTTTTGGAG | 81858 |
| rs778572874 | snp | A/G | 1.74017e-05 | 0.00294967 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099212 | GTCCTGTGGCTGAGG[A/G]GGTGGAGCTCAGGAC | 81858 |
| rs778597535 | in-del | -/G | 1.6696e-05 | 0.00288924 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105778 | CAGGTGAGGCAGGCT[-/G]GGGGGGGCTGGCATC | 81858 |
| rs778667823 | snp | C/G | 1.80917e-05 | 0.00300758 | intron-variant | SHARPIN | GRCh38.p7 | 8:144100076 | TCTTGCTGCCTAGAG[C/G]TAAGATATGGGTGTG | 81858 |
| rs778687416 | in-del | -/GATGCGGCA | 3.33918e-05 | 0.00408592 | cds-indel, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099579 | GCAGAGGACGCGGCG[-/GATGCGGCA]GATGCGGCAGAGGCA | 81858 |
| rs778975473 | snp | A/G | 1.66205e-05 | 0.00288271 | upstream-variant-2KB, missense | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106207 | TCAGCACAGCCCGCA[A/G]CCATGAGTTCAGCCG | 81858 |
| rs778985406 | snp | A/G | 2.75456e-05 | 0.00371107 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103630 | TCAGCTGCAGCCTCC[A/G]CAGCTGTGCCTCGGC | 81858 |
| rs779040311 | snp | C/G | 3.33762e-05 | 0.00408497 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099678 | GGTCACGAGGACAAG[C/G]TGAAGAAGCAGCCCC | 81858 |
| rs779040465 | snp | A/T | 1.66153e-05 | 0.00288225 | upstream-variant-2KB, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105645 | CACTCCCCAGGCAAT[A/T]CTAGCCCCTCTGGAG | 81858 |
| rs779058225 | in-del | -/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SHARPIN, MAF1 | GRCh38.p7 | 8:144105030 | CCCCAGCGGGGCCGA[-/G]GGGACCGCCCTCCTA | 81858 |
| rs779153022 | snp | C/T | 1.67863e-05 | 0.00289704 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099010 | CTGGGGGAAGAGAGA[C/T]AGTTGTTGCTTCCCT | 81858 |
| rs779172807 | snp | C/G | 1.70974e-05 | 0.00292376 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099471 | GATGTCACCTAGGCT[C/G]CTCTGCCCCTGGCAG | 81858 |
| rs779222252 | snp | A/G | 1.76409e-05 | 0.00296987 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099084 | TCCCGTGCCCACCTG[A/G]AGTGGACTGGGCAGG | 81858 |
| rs779278706 | snp | A/G | 1.79403e-05 | 0.00299497 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103264 | TCAGGGCGTCCCCCC[A/G]CCCTACATCGCACGA | 81858 |
| rs779409863 | in-del | -/TTG | 1.65067e-05 | 0.00287282 | cds-indel, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099369 | TGCGCTCAGGCACAC[-/TTG]ACAGGCACCGTCCGA | 81858 |
| rs779415875 | snp | C/T | 1.6701e-05 | 0.00288968 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099564 | CTGCAGGGCAACGTG[C/T]GCAGAGGACGCGGCG | 81858 |
| rs779424609 | snp | A/T | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105272 | TCCCGTTGCGGACTC[A/T]AGAGTTACCCCCATG | 81858 |
| rs779647452 | in-del | -/T | 1.78144e-05 | 0.00298444 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103257 | TCCAGGCTCAGGGCG[-/T]CCCCCCGCCCTACAT | 81858 |
| rs779681158 | snp | A/C/G | 0.000133164 | 0.00815885 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105832 | TTCAGTGGAACCTGG[A/C/G]GGAAGCATGCTTCAT | 81858 |
| rs779853100 | snp | A/G | 1.71734e-05 | 0.00293026 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099997 | CCCTTGAGTGTGGAG[A/G]CTTCCGGGGGACTGG | 81858 |
| rs779931716 | snp | A/G | 0.000107373 | 0.00732632 | synonymous-codon, intron-variant | SHARPIN | GRCh38.p7 | 8:144099117 | GGAGGCAGCTGGCTG[A/G]GGGCCTGGGGGTAGC | 81858 |
| rs780070016 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144098726 | TCAGTAGAGGTCCCC[A/G]GAGTTCAGTGGGGGC | 81858 |
| rs780204048 | snp | A/C/G | 6.70854e-05 | 0.00579129 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099004 | GCTGGGCTGGGGGAA[A/C/G]AGAGACAGTTGTTGC | 81858 |
| rs780264021 | snp | A/G | 5.02037e-05 | 0.00500993 | synonymous-codon, nc-transcript-variant, missense | SHARPIN | GRCh38.p7 | 8:144098947 | CATCTCACAGCCAGG[A/G]CGGTCTGGGGCATTG | 81858 |
| rs780283653 | snp | A/G | 1.66385e-05 | 0.00288426 | missense, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103096 | CTAGGACTGCCCACC[A/G]CTGAGCTTCCTGAGG | 81858 |
| rs780307845 | snp | A/G | 0.000117668 | 0.00766942 | synonymous-codon, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099774 | ATGCTGGGCCAGGAC[A/G]GCTGCCACTTGGGCT | 81858 |
| rs780341921 | in-del | -/GGCCCC | | | intron-variant | SHARPIN | GRCh38.p7 | 8:144100685 | CCCAGCGCTGTTCCT[-/GGCCCC]GGCCCCGGCCCCGGC | 81858 |
| rs780365154 | snp | C/G | 1.69519e-05 | 0.0029113 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099827 | CAATAGCCCGGGCCA[C/G]GCTCCCTGCCAGCTC | 81858 |
| rs780385793 | snp | A/G | 8.34578e-05 | 0.00645925 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103166 | TGGAGGCTGTAGCTC[A/G]TGCTGGGTGGGGCCT | 81858 |
| rs780650155 | snp | C/T | 1.70863e-05 | 0.00292281 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099455 | GAGCATCAGGGCAGG[C/T]GATGTCACCTAGGCT | 81858 |
| rs780691915 | snp | A/G | 0.000134228 | 0.00819122 | missense, nc-transcript-variant | SHARPIN | GRCh38.p7 | 8:144099394 | GTCCGATGACCCAGC[A/G]TTGCACGGCTGGCGG | 81858 |
| rs780918459 | snp | G/T | 0.0211949 | 0.100738 | upstream-variant-2KB, splice-donor-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105768 | CACATCATTGGCAGG[G/T]GAGGCAGGCTGGGGG | 81858 |
| rs780935480 | snp | C/T | 1.70321e-05 | 0.00291818 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099445 | CCTGTGGCCAGAGCA[C/T]CAGGGCAGGTGATGT | 81858 |
| rs780973441 | snp | A/C | 3.3295e-05 | 0.00408 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144105820 | ACTGCCGCGCCCTTC[A/C]GTGGAACCTGGGGGA | 81858 |
| rs781032080 | snp | A/G | 1.77432e-05 | 0.00297847 | missense, intron-variant | SHARPIN | GRCh38.p7 | 8:144099103 | GGACTGGGCAGGCTG[A/G]AGGCAGCTGGCTGGG | 81858 |
| rs781046660 | snp | A/G | 1.71537e-05 | 0.00292857 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099857 | CTTCTGCAGGGTAAG[A/G]AAAGGACAGCTGTCA | 81858 |
| rs781087096 | snp | A/G | 7.47971e-05 | 0.00611498 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103534 | GAGGACTGACCGCGC[A/G]CCCTCCGCCCCCACT | 81858 |
| rs781179957 | snp | C/G | 1.6884e-05 | 0.00290547 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099029 | TGTTGCTTCCCTGCT[C/G]TTTCCAATGCCCATG | 81858 |
| rs781340614 | snp | A/G | 0.000951384 | 0.0217896 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103613 | CCGCTCAGGGTCCGC[A/G]CTCAGCTGCAGCCTC | 81858 |
| rs781425333 | snp | C/T | 8.33104e-05 | 0.00645355 | upstream-variant-2KB, intron-variant | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106052 | GGGAGGTGATGGGCC[C/T]AGCTGATGGTTCTGT | 81858 |
| rs781465438 | snp | A/G | 1.66874e-05 | 0.0028885 | intron-variant | SHARPIN | GRCh38.p7 | 8:144099672 | TGGGATGGTCACGAG[A/G]ACAAGGTGAAGAAGC | 81858 |
| rs781621683 | snp | A/G | 6.67034e-05 | 0.00577471 | intron-variant, upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144103042 | TTGTATCCATTACAG[A/G]GCACTGACCATTCTG | 81858 |
| rs781680999 | snp | G/T | | | upstream-variant-2KB | SHARPIN, MAF1 | GRCh38.p7 | 8:144104274 | CCTCACTGGTTACGG[G/T]GTCGACCCCCCTAGG | 81858 |
| rs781721737 | snp | C/T | 1.66579e-05 | 0.00288595 | upstream-variant-2KB, synonymous-codon | WDR97, SHARPIN, MAF1 | GRCh38.p7 | 8:144106149 | AAGACCCTCTTCTAC[C/T]TGATTGCCACGCTCA | 81858 |
| rs781737565 | snp | C/G | | | upstream-variant-2KB, intron-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144105409 | TAGTCCCAGAACTCG[C/G]GTGTTCTGCAGGGGG | 81858 |
| rs781778009 | snp | C/T | 3.32784e-05 | 0.00407898 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SHARPIN, MAF1 | GRCh38.p7 | 8:144103076 | TTCCACGGTGGCACC[C/T]CGGACTAGGACTGCC | 81858 |
| rs781779024 | in-del | -/GGCTGGAGGCAGCT | 1.77505e-05 | 0.00297908 | frameshift-variant, intron-variant | SHARPIN | GRCh38.p7 | 8:144099098 | GGAGTGGACTGGGCA[-/GGCTGGAGGCAGCT]GGCTGGGGGCCTGGG | 81858 |