SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3602 | snp | C/T | 0.238171 | 0.24972 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986441 | ACGCACTAAAAAAAA[C/T]GTGTGCTTGCTGCTG | 81929 |
rs8566 | snp | G/T | 0.319376 | 0.240181 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985601 | TGAACTAAAGTGGTA[G/T]TCCCCTCCTCCCAAC | 81929 |
rs489221 | snp | C/G/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978818 | AGATCTTCCCAAATT[C/G/T]GGAGCGAATGCAATA | 81929 |
rs498816 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967727 | gagactagcctggcc[A/C]acacagcgaaaccct | 81929 |
rs498888 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967760 | ttctactaaaaatac[A/C]aaaattagatgggcg | 81929 |
rs503063 | snp | A/C/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978858 | CTAGCCATAGCGACC[A/C/G]AAGATGTGAGAATTT | 81929 |
rs522801 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12951317 | TTAGGTAACAGAGAC[A/C]ATTAGTTACAGTCAC | 81929 |
rs527830 | snp | A/C | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12970793 | CATTAACTATGAAAC[A/C]AAAAGTAACCCTACT | 81929 |
rs527909 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970760 | GACTAACTTCATGAC[A/C]AAAAGATCTTAAGTG | 81929 |
rs528699 | snp | G/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12963018 | GTACTTGTAGGAACT[G/T]GTGGCCCAGAGATGt | 81929 |
rs612704 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12952784 | aaaaaaaaaaaaaaa[A/G]aaaagaagagaagag | 81929 |
rs616062 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967884 | ctctgttgcccaggc[G/T]ggagtgcagtggcat | 81929 |
rs616083 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967874 | caggctggagtgcag[G/T]ggcatcatcttggct | 81929 |
rs616100 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967863 | gcagtggcatcatct[G/T]ggctcactgcaacct | 81929 |
rs621350 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962997 | CTACAAGTACATGGC[A/C]AAATACCACATATAT | 81929 |
rs621878 | snp | A/C | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12962871 | TAATCTCTCTTAAGC[A/C]AACTGATCACAAAAA | 81929 |
rs640682 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970737 | AGTGTTTCTTCTTTT[G/T]GTCAAAGCACTTAAG | 81929 |
rs651176 | snp | A/C | 0 | 0 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978761 | CATTAGGAAATATGC[A/C]AAAGCTGAAACTCTT | 81929 |
rs651632 | snp | A/C | 0 | 0 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978848 | TTTCCATATTCTAGC[A/C]ATAGCGACCAAAGAT | 81929 |
rs652076 | snp | C/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12978946 | TGCCTTCTGATTACC[C/T]TTGTTTGTGGAGGAG | 81929 |
rs977104 | snp | C/G | 0.277334 | 0.248501 | intron-variant | SEH1L | GRCh38.p7 | 18:12982892 | GTTGTAATTACTTTA[C/G]TTTTGAAAACTGCTC | 81929 |
rs1300125 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958166 | aaccccggaggcgga[A/G]aatgcagtaagccga | 81929 |
rs1474043 | snp | C/T | 0.354235 | 0.227234 | intron-variant | SEH1L | GRCh38.p7 | 18:12951739 | TAGTTAACAAAAGAA[C/T]ACAATCAGCAAGTAA | 81929 |
rs1523064 | snp | A/T | 0.463881 | 0.12944 | intron-variant | SEH1L | GRCh38.p7 | 18:12982265 | TTTCTTTCTTCCATG[A/T]AACAGTCACTGAGTA | 81929 |
rs1964084 | snp | A/G | 0.414741 | 0.188044 | intron-variant | SEH1L | GRCh38.p7 | 18:12981071 | ttctcagacggggcg[A/G]ttgccaggcagaggg | 81929 |
rs1971424 | snp | A/G | 0.481856 | 0.0935034 | intron-variant | SEH1L | GRCh38.p7 | 18:12969040 | TATTTTTAGTAGAGA[A/G]GGGTTTTCTCCATGT | 81929 |
rs2014404 | snp | C/T | 0.494936 | 0.050064 | intron-variant | SEH1L | GRCh38.p7 | 18:12981431 | TGAGCACTGAGTGAA[C/T]GCAACTCCGTCTGCC | 81929 |
rs2902856 | snp | A/C | 0.349013 | 0.229557 | intron-variant | SEH1L | GRCh38.p7 | 18:12984341 | TTCATTTTGTTAGCT[A/C]TGTATTTGGCTTACT | 81929 |
rs3070220 | in-del | -/TTTT | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962485 | ttttttttttttttt[-/TTTT]gagagagggtcttac | 81929 |
rs3809911 | snp | A/G | 0.067446 | 0.170804 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947361 | CTTCGCTCTTAGGCT[A/G]CCGAGCCTGGACTGC | 81929 |
rs3809912 | snp | C/T | 0.339656 | 0.233371 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947463 | CAAACCCACGGTTCG[C/T]CTTCTCCACCTGCTC | 81929 |
rs3809913 | snp | C/G | 0.0498117 | 0.149749 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947484 | CCACCTGCTCCGCGC[C/G]CCTCGCATGTGTCTG | 81929 |
rs3809914 | snp | C/T | 0.419936 | 0.183362 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947617 | AAGCTCTTACTACTT[C/T]TCAGCACAGGTAACT | 81929 |
rs3840889 | in-del | -/T | 0.467946 | 0.122472 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946933 | CCTTCTGCAGCCTCA[-/T]TTTTTTTTTTTCTGT | 81929 |
rs3976787 | snp | C/T | 0.416218 | 0.186739 | intron-variant | SEH1L | GRCh38.p7 | 18:12971895 | TGCATGTGGTAAGGC[C/T]GTGAGCAAGAGAGAG | 81929 |
rs4797721 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949616 | cgccaccacgcccgg[C/G]taattttttgtattt | 81929 |
rs4995995 | snp | A/C | 0.354235 | 0.227234 | intron-variant | SEH1L | GRCh38.p7 | 18:12954741 | GTGGCTCACGCCTGT[A/C]TTCTCAGCCCTTTAG | 81929 |
rs6505773 | snp | A/G | 0.49907 | 0.0215454 | intron-variant | SEH1L | GRCh38.p7 | 18:12974092 | GGTGTTGGGGAAAGA[A/G]TGTCTGCAGGTGGGG | 81929 |
rs6505774 | snp | G/T | 0.484421 | 0.0868729 | intron-variant | SEH1L | GRCh38.p7 | 18:12976468 | tctctgccacaGTAC[G/T]GGTGTTCCTCCCACT | 81929 |
rs6505775 | snp | C/T | 0.349013 | 0.229557 | intron-variant | SEH1L | GRCh38.p7 | 18:12978184 | CTAAATGTACATTAT[C/T]AAAGGAGGAAACGTG | 81929 |
rs6505776 | snp | A/C | 0.437409 | 0.165462 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984145 | CTTCCCTAGGTTCAA[A/C]TATTCCAAGTCTTCA | 81929 |
rs7227812 | snp | A/G | 0.499 | 0.0223418 | intron-variant | SEH1L | GRCh38.p7 | 18:12976561 | TGTGCTCTTAGCTCC[A/G]CCTGTCCTATTTCTG | 81929 |
rs7228108 | snp | C/T | 0.26078 | 0.249767 | intron-variant | SEH1L | GRCh38.p7 | 18:12976656 | TTATAGGTACTGAAA[C/T]CATGGGTGTAGAAAC | 81929 |
rs7228122 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | SEH1L | GRCh38.p7 | 18:12976687 | CATGCATATTCTGGC[C/T]GGGCGCAGTGGCTCA | 81929 |
rs7233600 | snp | A/G | 0.34989 | 0.229177 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986001 | CTTATATACATTTGT[A/G]TATTTTTATGGTGTT | 81929 |
rs7236729 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | SEH1L | GRCh38.p7 | 18:12953345 | tctgtgtagacatat[A/G]ttttcatttcttttg | 81929 |
rs7237381 | snp | C/G | 0.11228 | 0.208646 | intron-variant | SEH1L | GRCh38.p7 | 18:12953664 | tccaaGGTCCCCCCC[C/G]CTTttaaggtgaggt | 81929 |
rs7359710 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12985020 | ATCAAAACAATTTCA[A/G]GTTACCGTGGAAGAT | 81929 |
rs7506801 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | SEH1L | GRCh38.p7 | 18:12954711 | gggctcaagcagtct[G/T]cccacctcagccccc | 81929 |
rs8083401 | snp | C/T | 0.416218 | 0.186739 | intron-variant | SEH1L | GRCh38.p7 | 18:12967651 | gggcacagtggctca[C/T]gcctgttatcccagc | 81929 |
rs8083472 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12976109 | gaaacagtacagatt[C/T]ggtatttcaatgtct | 81929 |
rs8085257 | snp | C/T | 0.0402882 | 0.136092 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946529 | tcactcccactctga[C/T]aatctctggcaacca | 81929 |
rs8086882 | snp | C/G | 0.467132 | 0.12391 | intron-variant | SEH1L | GRCh38.p7 | 18:12982135 | CCTCCCAAAGTGCTG[C/G]GATTACAGGTGTGAG | 81929 |
rs8088313 | snp | A/C | 0.349452 | 0.229367 | intron-variant | SEH1L | GRCh38.p7 | 18:12977207 | AAAGAAGGTCAAGTG[A/C]AGAATGCTGTAGAAA | 81929 |
rs8089123 | snp | A/G | 0.350109 | 0.229081 | intron-variant | SEH1L | GRCh38.p7 | 18:12970263 | TTAAAAAGTCATTCA[A/G]CTTATAGTTCAGGAG | 81929 |
rs8089189 | snp | C/T | 0.412249 | 0.190198 | intron-variant | SEH1L | GRCh38.p7 | 18:12970467 | ACTCTGTTGCCCAGG[C/T]TAGAGTGCAGTGGCA | 81929 |
rs8090667 | snp | A/C | 0.445987 | 0.155207 | intron-variant | SEH1L | GRCh38.p7 | 18:12974074 | TCAAAAACGAGGGGA[A/C]GTGGTGTTGGGGAAA | 81929 |
rs8092888 | snp | A/G | 0.477684 | 0.103247 | intron-variant | SEH1L | GRCh38.p7 | 18:12978067 | tactgggttcaagca[A/G]ttctcccacctcagc | 81929 |
rs8093576 | snp | C/G | 0.426507 | 0.177046 | intron-variant | SEH1L | GRCh38.p7 | 18:12978290 | actcacagttctgga[C/G]gtcggaagtctgaaa | 81929 |
rs8096596 | snp | A/T | 0.498982 | 0.0225409 | intron-variant | SEH1L | GRCh38.p7 | 18:12966561 | TTCACCACCATGCCT[A/T]GCTAATTTTTTGTTA | 81929 |
rs8099508 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SEH1L | GRCh38.p7 | 18:12951290 | tgctgtttaaaatgg[C/T]ctccaagcgtagtgA | 81929 |
rs8182426 | snp | C/G | 0.201836 | 0.245317 | intron-variant | SEH1L | GRCh38.p7 | 18:12978734 | CTAAAATGTTAATGT[C/G]AATTGTTTTTCCATT | 81929 |
rs9748518 | snp | C/T | 0.350327 | 0.228986 | intron-variant | SEH1L | GRCh38.p7 | 18:12979221 | GACCCTGCGGCCTTC[C/T]GCAGTGTTTGTGTCC | 81929 |
rs9748528 | snp | C/T | 0.350982 | 0.228698 | intron-variant | SEH1L | GRCh38.p7 | 18:12979435 | gaatttttcttagta[C/T]agaacaaaatgaaaa | 81929 |
rs9748873 | snp | A/G | 0.350982 | 0.228698 | intron-variant | SEH1L | GRCh38.p7 | 18:12979436 | aatttttcttagtat[A/G]gaacaaaatgaaaag | 81929 |
rs9946408 | snp | A/C | 0.412416 | 0.190055 | intron-variant | SEH1L | GRCh38.p7 | 18:12968759 | GGAGATCCAGGTGAT[A/C]TGTCTACACTATTCA | 81929 |
rs9947799 | snp | C/T | 0.42574 | 0.177808 | intron-variant | SEH1L | GRCh38.p7 | 18:12956924 | TACAAAAAATTAGCC[C/T]GGCATGGTGGTGGGT | 81929 |
rs9948681 | snp | A/C | 0.369958 | 0.21934 | intron-variant | SEH1L | GRCh38.p7 | 18:12974738 | GTTTATATAGGTTAC[A/C]GGGCATTTTTATGTG | 81929 |
rs9949126 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12969069 | tacaaaattagctgg[G/T]tttggtggcacatgc | 81929 |
rs9949380 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | SEH1L | GRCh38.p7 | 18:12953062 | gctgggattacaggc[G/T]tgagccaccatgcct | 81929 |
rs9949475 | snp | C/T | 0.412249 | 0.190198 | intron-variant | SEH1L | GRCh38.p7 | 18:12969516 | aacatggtgaaacct[C/T]atctttactaaagat | 81929 |
rs9949532 | snp | C/G | 0.389152 | 0.207694 | intron-variant | SEH1L | GRCh38.p7 | 18:12962367 | tgacagagcaagacc[C/G]tgtccctaagaaaaa | 81929 |
rs9949863 | snp | C/T | 0.176219 | 0.238865 | intron-variant | SEH1L | GRCh38.p7 | 18:12953517 | CTGTCTTTTTTATTA[C/T]AGCCATTTTAGTAGT | 81929 |
rs9950241 | snp | C/T | 0.44768 | 0.153045 | intron-variant | SEH1L | GRCh38.p7 | 18:12957024 | agtgagccgagatca[C/T]gccactgcactccag | 81929 |
rs9951081 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | SEH1L | GRCh38.p7 | 18:12957948 | tcctggactgaagca[A/G]tcctctcacctcggc | 81929 |
rs9951490 | snp | G/T | 0.485118 | 0.0849685 | intron-variant | SEH1L | GRCh38.p7 | 18:12966059 | GATTAATCTTACTTA[G/T]CACTTACCATTTGTT | 81929 |
rs9953795 | snp | C/T | 0.118235 | 0.212457 | intron-variant | SEH1L | GRCh38.p7 | 18:12951120 | ttgcagtcatttgtg[C/T]atgtgtgaggagtgg | 81929 |
rs9954360 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SEH1L | GRCh38.p7 | 18:12951611 | gtctaggctggtctc[A/G]aactcctgacctcag | 81929 |
rs9958369 | snp | C/G | 0.349452 | 0.229367 | intron-variant | SEH1L | GRCh38.p7 | 18:12977631 | CAGGAGGCTGAAGCA[C/G]GAGAATCACTTGAAC | 81929 |
rs9960379 | snp | C/T | 0.17654 | 0.238964 | intron-variant | SEH1L | GRCh38.p7 | 18:12953270 | ctgttcaccagttga[C/T]ggacatttgagttgt | 81929 |
rs9964329 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949034 | tttttttttttttgt[A/G]ttttttagtagagac | 81929 |
rs9964794 | snp | A/G | 0.274124 | 0.248833 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949295 | AGTAACTGGAAATCT[A/G]AAGGATAGTTTATCC | 81929 |
rs9965936 | snp | G/T | 0.118235 | 0.212457 | intron-variant | SEH1L | GRCh38.p7 | 18:12951077 | GTCTACTCTGAAATT[G/T]ACTTGTACCCcaaaa | 81929 |
rs9965977 | snp | G/T | 0.368938 | 0.219895 | intron-variant | SEH1L | GRCh38.p7 | 18:12958329 | gatctcaaatgattc[G/T]cctgccttggcctcc | 81929 |
rs10541594 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956455 | TGTGTCTGGGGAATC[-/A]AAAAAAAAAAAAGAA | 81929 |
rs11080616 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | SEH1L | GRCh38.p7 | 18:12962000 | AGTTTCATCTTATCT[A/G]TGTGCCAGAAGATAA | 81929 |
rs11080617 | snp | A/G | 0.326976 | 0.237854 | intron-variant | SEH1L | GRCh38.p7 | 18:12968508 | ACTCCATGATTGTCC[A/G]TGACTCATTTATATT | 81929 |
rs11286163 | in-del | -/T | 0.0179954 | 0.0931336 | intron-variant | SEH1L | GRCh38.p7 | 18:12955441 | GTATCTGTTCTTTTC[-/T]TTTTTTTTTTTGATT | 81929 |
rs11314030 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949215 | TGAGATTTAGGAACC[-/T]CCCAGATGTGTTGCA | 81929 |
rs11351617 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964653 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 81929 |
rs11480632 | in-del | -/T/TT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986813 | TTGTGTTTTTTTTTT[-/T/TT]CCTGTTTTTGTTTTG | 81929 |
rs11548616 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985372 | CCAAGATACACCAGC[A/G]GCCTGCTTACTACTA | 81929 |
rs11548617 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985541 | GTTCCTGAAACTAAT[C/T]TGGGTTTAAAGATTA | 81929 |
rs11661908 | snp | C/T | 0.465996 | 0.12588 | intron-variant | SEH1L | GRCh38.p7 | 18:12981827 | TTCCATTCTTTCATT[C/T]TTTCCTACTTGCTGC | 81929 |
rs11663762 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SEH1L | GRCh38.p7 | 18:12953790 | catttttattattcc[A/G]aaaggaaaccccatC | 81929 |
rs11876664 | snp | G/T | 0.444444 | 0.157135 | intron-variant | SEH1L | GRCh38.p7 | 18:12962664 | ttttagtagagacgg[G/T]gtcttgccatgtagc | 81929 |
rs11876742 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | SEH1L | GRCh38.p7 | 18:12966183 | CTGCAAGCTCCGCCT[C/T]CTGGGTTTAAGAGAT | 81929 |
rs12232629 | snp | G/T | 0.303438 | 0.244222 | intron-variant | SEH1L | GRCh38.p7 | 18:12981146 | acatctcagatgatg[G/T]gcggccgggcagaga | 81929 |
rs12326946 | snp | C/G | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947226 | TTCTACAGGCGGACT[C/G]TTCTAATTCATACTA | 81929 |
rs12457672 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971434 | AAGAGGAGAAAGTag[A/C]ccagcctggccaata | 81929 |
rs12604345 | snp | C/T | 0.46974 | 0.119223 | intron-variant | SEH1L | GRCh38.p7 | 18:12968224 | AACAACTTACTCTCT[C/T]AACTAGGGAGGCTGA | 81929 |
rs12605267 | snp | A/G | 0.318656 | 0.240388 | intron-variant | SEH1L | GRCh38.p7 | 18:12957416 | CTGGGGAACAAGAGC[A/G]AGACTTCGTCTCAAA | 81929 |
rs12954256 | snp | C/T | 0.378372 | 0.214524 | intron-variant | SEH1L | GRCh38.p7 | 18:12959060 | tgtgttgtgaagtgg[C/T]atctccattgtggtt | 81929 |
rs12955780 | snp | A/G | 0.34146 | 0.23267 | intron-variant | SEH1L | GRCh38.p7 | 18:12982761 | TCTGAAATATTTTTT[A/G]AAAATGGTCTTTTAC | 81929 |
rs12961596 | snp | C/G | 0.448066 | 0.152544 | intron-variant | SEH1L | GRCh38.p7 | 18:12969750 | GGAAGTTTGTGGCCA[C/G]GTGTGGTGGTTCACG | 81929 |
rs12964252 | snp | C/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12975380 | GCAGCATGGACTGTA[C/T]TAAGAGCTGAAGGAG | 81929 |
rs12967249 | snp | C/T | 0.328148 | 0.237472 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949601 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 81929 |
rs12968052 | snp | G/T | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949443 | AAACTACGTTAACCG[G/T]ttttttttttttttt | 81929 |
rs12968559 | snp | A/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12981850 | CTTGCTGCCCTGCCC[A/T]ttttttttttttttt | 81929 |
rs12970503 | snp | A/G | 0.445987 | 0.155207 | intron-variant | SEH1L | GRCh38.p7 | 18:12955235 | AACTGGACTTCAGAA[A/G]CATTACAATCCTAAA | 81929 |
rs28377612 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | SEH1L | GRCh38.p7 | 18:12969492 | CAGGAGATCAAGACC[A/G]TCCTGGCCAACATGG | 81929 |
rs28534710 | snp | A/G | 0.47666 | 0.105476 | intron-variant | SEH1L | GRCh38.p7 | 18:12961400 | AGAGAAAGTTTAACA[A/G]CTGCCTGATCATCAC | 81929 |
rs28547349 | snp | A/C | 0.429837 | 0.173662 | intron-variant | SEH1L | GRCh38.p7 | 18:12957749 | TACCCCTCACCTGCC[A/C]TCCCTAATGGCATGA | 81929 |
rs28550089 | snp | C/T | 0.21875 | 0.248039 | intron-variant | SEH1L | GRCh38.p7 | 18:12950582 | GTTGTACTGAAATTT[C/T]TCATTAGTTTAGCAT | 81929 |
rs28579212 | snp | C/G | 0.118235 | 0.212457 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947277 | CTCCTAGCACCCCCA[C/G]GCCTGTTCTACCTGT | 81929 |
rs28622491 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | SEH1L | GRCh38.p7 | 18:12974791 | CAACCACCTTGTAAG[G/T]AGAGGAGACAGCTTT | 81929 |
rs28671274 | snp | A/G | 0.499203 | 0.0199521 | intron-variant | SEH1L | GRCh38.p7 | 18:12957771 | ATGGCATGATACTAC[A/G]TTAGAGCCAGTCACA | 81929 |
rs28735037 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | SEH1L | GRCh38.p7 | 18:12969504 | ACCATCCTGGCCAAC[A/G]TGGTGAAACCTCATC | 81929 |
rs34166083 | snp | C/T | 0.328382 | 0.237395 | intron-variant | SEH1L | GRCh38.p7 | 18:12961735 | GCAGTGGCATGATCT[C/T]GGCTCAGTGCAGCCT | 81929 |
rs34198242 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978817 | TATTGCATTCGCTCC[-/C]AAATTTGGGAAGATC | 81929 |
rs34236518 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962768 | TAAGCCATCACGCCC[-/C]AACTCATTTACAGTT | 81929 |
rs34381701 | in-del | -/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986741 | GCTTTTTTTTTTTTT[-/T]CTAGCATGTGTTTTC | 81929 |
rs34549663 | in-del | -/T | 0.473543 | 0.111932 | intron-variant | SEH1L | GRCh38.p7 | 18:12967050 | ACTATTTCCCTGTGG[-/T]TTTCTAGTGAAGATT | 81929 |
rs34660430 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970930 | CCATAAGAATATGCT[-/A]AAAAACAGTTCATAA | 81929 |
rs34677616 | in-del | -/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12983460 | CTTTTCTGCCTTTAG[-/G]CTTTATTCAGGACCA | 81929 |
rs34738452 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12973308 | ATTTTTTTTTTTTTT[-/T]GAGAGTCTCACTCTG | 81929 |
rs35029907 | in-del | -/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965282 | TCCCAAACTGCTGGG[-/G]ATTACAGGCATGAGC | 81929 |
rs35133318 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977452 | ATTCCTGCTGGGCGC[-/C]AGTGGCTCACACCTG | 81929 |
rs35368962 | snp | C/T | 0.446118 | 0.155041 | intron-variant | SEH1L | GRCh38.p7 | 18:12962502 | AGAGAGGGTCTTACT[C/T]TGTCACCCAGGCTGG | 81929 |
rs35556009 | in-del | -/A | 0.406468 | 0.194981 | intron-variant | SEH1L | GRCh38.p7 | 18:12972901 | TGTAGACATAAGCCC[-/A]AAAACGTAAAAGGTG | 81929 |
rs35889009 | in-del | -/T | 0.483708 | 0.088773 | intron-variant | SEH1L | GRCh38.p7 | 18:12966095 | TTTTTATTTTTATGG[-/T]TTTTTTTTTTTTTTG | 81929 |
rs35999381 | in-del | -/T | 0.932732 | 0.113673 | intron-variant | SEH1L | GRCh38.p7 | 18:12963148 | TTTAAATTGTTATTA[-/T]TTTTTTTTTAGGTTA | 81929 |
rs56263236 | snp | C/T | 0.433673 | 0.1696 | intron-variant | SEH1L | GRCh38.p7 | 18:12979029 | TAAAAATGTAAACTT[C/T]GAAATGTTTTTTAAA | 81929 |
rs56319921 | in-del | -/T | 0.360421 | 0.224293 | intron-variant | SEH1L | GRCh38.p7 | 18:12979076 | TTTCTTTTTTTTTTT[-/T]ATTGATCATTCTTGG | 81929 |
rs56774587 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SEH1L | GRCh38.p7 | 18:12951452 | CTGGAGTGCAGTGGC[A/G]TGATGTCAGCTCACT | 81929 |
rs56845444 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | SEH1L | GRCh38.p7 | 18:12958187 | CTCCGGGGTTCAAGC[A/G]ATTTTCCTGCCTCAG | 81929 |
rs56915491 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953109 | TCTAGAAATTTCATA[A/G]AAATGGAATTTTGAA | 81929 |
rs57012663 | snp | A/G | 0.166832 | 0.235761 | intron-variant | SEH1L | GRCh38.p7 | 18:12954341 | GCCAACAGGAGGGGT[A/G]TAAGGATTTGGGCTT | 81929 |
rs57267022 | in-del | -/C | 0.310386 | 0.242597 | intron-variant | SEH1L | GRCh38.p7 | 18:12985012 | GTACATGCATCAAAA[-/C]AATTTCAGGTTACCG | 81929 |
rs57277014 | snp | A/G | 0.142947 | 0.22592 | intron-variant | SEH1L | GRCh38.p7 | 18:12971569 | AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 81929 |
rs57472937 | snp | A/T | 0.203267 | 0.245593 | intron-variant | SEH1L | GRCh38.p7 | 18:12975003 | TTTTTATTTTATTTT[A/T]TTTTTTGAGATGAAG | 81929 |
rs57503635 | snp | C/G | 0.021333 | 0.101051 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947557 | GAGGACCGTGAGAGG[C/G]AGTCTTCACTTTTTC | 81929 |
rs57535684 | snp | A/G | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987891 | TTAGAATATTTTCTA[A/G]AATATTTTAAAATGA | 81929 |
rs57635324 | in-del | -/AAAAAA/AAAAAAAA | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12971645 | CCTCAAAAAAAAAAA[-/AAAAAA/AAAAAAAA]GAGGAGAAGGTAATT | 81929 |
rs57692810 | snp | C/T | 0.164219 | 0.234823 | intron-variant | SEH1L | GRCh38.p7 | 18:12970527 | CTGGGCGCAAGTGAT[C/T]CTCCTGCCTCAGCTC | 81929 |
rs57733399 | in-del | -/TTTTTTTTTTT | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958091 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GAGACAGAGTCTTGT | 81929 |
rs57834325 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SEH1L | GRCh38.p7 | 18:12950773 | CATTTTTAACAGGTG[A/G]AATTGGCACCTTCTT | 81929 |
rs58172687 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953710 | TAATTTCAGAGTAAA[-/A]CAATTAATTGGCATT | 81929 |
rs58458627 | in-del | -/T | 0.190519 | 0.242821 | intron-variant | SEH1L | GRCh38.p7 | 18:12974993 | TTTTATTTTTATTTT[-/T]ATTTTTTTTTTTGAG | 81929 |
rs58537161 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | SEH1L | GRCh38.p7 | 18:12956337 | GTGAGCCACCACGCC[C/T]GGCCAAGGGTTAATA | 81929 |
rs58764311 | snp | A/G | 0.263809 | 0.249618 | intron-variant | SEH1L | GRCh38.p7 | 18:12978485 | GAATACTTACTGCAC[A/G]TTGGATTTAGGACCC | 81929 |
rs59647001 | snp | A/G | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987711 | ATGTATTTTATTTAA[A/G]ATAATTGCCAAGGCT | 81929 |
rs59664947 | snp | A/G | 0.164219 | 0.234823 | intron-variant | SEH1L | GRCh38.p7 | 18:12972907 | CATAAGCCCAAAAAC[A/G]TAAAAGGTGTATCAT | 81929 |
rs59814486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12953045 | CCTTGGCCTTCCAAA[A/G]TGCTGGGATTACAGG | 81929 |
rs59844990 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12952909 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACAG | 81929 |
rs60273686 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12952838 | CCAGGCTGGAGTGCA[A/G]TGGTGCGATGTTGGC | 81929 |
rs60383179 | snp | C/G | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947661 | GCACCCTCCGCCGCC[C/G]AACGGTCAGAGCCTG | 81929 |
rs60964320 | snp | A/G | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987671 | TATTTAAAAATATAC[A/G]AATCTCTTGCCTTAT | 81929 |
rs61123859 | in-del | -/AT | 0.264632 | 0.249571 | intron-variant | SEH1L | GRCh38.p7 | 18:12982793 | GTTACTTTTAATGTC[-/AT]ATTAATTTATGTTAT | 81929 |
rs61138002 | snp | A/G | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987807 | TTTATTTAAAAGGTA[A/G]AAAGTCAGTATGTAG | 81929 |
rs61304518 | snp | A/G | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987837 | GACTACTAACATTTA[A/G]AATGGACAGATGTTG | 81929 |
rs61310469 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | SEH1L | GRCh38.p7 | 18:12976585 | ATTTCTGGCCTTTGG[C/T]AGAAGGCCAGAATCT | 81929 |
rs61480660 | snp | A/G | 0.491834 | 0.0633738 | intron-variant | SEH1L | GRCh38.p7 | 18:12956439 | CCATACAGATCCACT[A/G]TGTGTCTGGGGAATC | 81929 |
rs61610540 | snp | A/T | 0.301681 | 0.2446 | intron-variant | SEH1L | GRCh38.p7 | 18:12979042 | TTTGAAATGTTTTTT[A/T]AAAATGGTCTTTTAC | 81929 |
rs62095793 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956450 | CACTGTGTGTCTGGG[A/G]AATCAAAAAAAAAAA | 81929 |
rs62095794 | snp | C/T | 0.142609 | 0.225759 | intron-variant | SEH1L | GRCh38.p7 | 18:12958106 | TTTTTTTTTTTGAGA[C/T]AGAGTCTTGTTCTGT | 81929 |
rs62095795 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SEH1L | GRCh38.p7 | 18:12961165 | TGTTTACTGGAGTTG[C/T]GCAGATGCTCACTTG | 81929 |
rs62095796 | snp | G/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12966109 | GTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTTG | 81929 |
rs62095797 | snp | C/T | 0.142947 | 0.22592 | intron-variant | SEH1L | GRCh38.p7 | 18:12970242 | TATGTTAATTAGGCA[C/T]AGAAATTAAAAAGTC | 81929 |
rs62095799 | snp | C/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12973454 | ACAAGTGCGTGCCAC[C/T]ACGCCTGGCTAATTT | 81929 |
rs62095800 | snp | A/G | 0.144632 | 0.226711 | intron-variant | SEH1L | GRCh38.p7 | 18:12977915 | CTCACTGCAACCTCC[A/G]CCTCCTGGGCTCAAG | 81929 |
rs62095801 | snp | A/C | 0.144632 | 0.226711 | intron-variant | SEH1L | GRCh38.p7 | 18:12978512 | ACCCACCCTAAATCT[A/C]GGATGTCATTCTGAG | 81929 |
rs62095802 | snp | C/T | 0.143959 | 0.226396 | intron-variant | SEH1L | GRCh38.p7 | 18:12979057 | AAAAATGGTCTTTTA[C/T]AGTTACTTTTTTTTC | 81929 |
rs62095804 | snp | C/G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12981264 | ATCCCAGACGATGGG[C/G/T]GGCCAGGCAGAGACG | 81929 |
rs62095825 | snp | A/G | 0.109578 | 0.206838 | intron-variant | SEH1L | GRCh38.p7 | 18:12984272 | GGTGGATTATTTCAT[A/G]GATTATAAGATGGAG | 81929 |
rs62095826 | snp | A/G | 0.143622 | 0.226238 | intron-variant | SEH1L | GRCh38.p7 | 18:12984967 | TTATGTTTTCATAAA[A/G]AAGTTCTGCTTTTGA | 81929 |
rs66484417 | snp | C/T | 0.375 | 0.216506 | intron-variant | SEH1L | GRCh38.p7 | 18:12955121 | CTTTGTTTCAAAGGT[C/T]GGTTACGCTAAACTC | 81929 |
rs66661616 | snp | A/T | 0.176861 | 0.239062 | intron-variant | SEH1L | GRCh38.p7 | 18:12960746 | CATAAGAAGGACTTT[A/T]CTTTGAATTTCAAGA | 81929 |
rs67068160 | snp | C/T | 0.237014 | 0.249662 | intron-variant | SEH1L | GRCh38.p7 | 18:12984346 | TTTGTTAGCTATGTA[C/T]TTGGCTTACTTGGTC | 81929 |
rs67415465 | snp | A/G | 0.238171 | 0.24972 | intron-variant | SEH1L | GRCh38.p7 | 18:12981717 | ATTTAATGACAAGTG[A/G]CAGTCTATTTAGGGA | 81929 |
rs67538562 | snp | C/G | 0.234401 | 0.249513 | intron-variant | SEH1L | GRCh38.p7 | 18:12978646 | CCACTACAGAGGTGA[C/G]CACTACATGATTGTG | 81929 |
rs67640584 | snp | G/T | 0.238171 | 0.24972 | intron-variant | SEH1L | GRCh38.p7 | 18:12985093 | GTTGATTTTTTAAAG[G/T]CTGGTTTTTGGTCAC | 81929 |
rs68004799 | snp | C/T | 0.319376 | 0.240181 | intron-variant | SEH1L | GRCh38.p7 | 18:12967225 | TCACTACATTTTTGT[C/T]AACTGATCAGTGTAT | 81929 |
rs71174155 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949470 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 81929 |
rs71174156 | in-del | -/A | 0.444 | 0.157683 | intron-variant | SEH1L | GRCh38.p7 | 18:12952193 | ACATAGTTTTCTCTT[-/A]AAAAAAAAAAACAAA | 81929 |
rs71174157 | in-del | -/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12958101 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT | 81929 |
rs71174159 | in-del | -/TT | 0 | 0 | downstream-variant-500B, utr-variant-3-prime | SEH1L | GRCh38.p7 | 18:12987573 | TTTTTTTTTTTTTTT[-/TT]AAAGGAAATTGCCTT | 81929 |
rs71353231 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949639 | TTGTATTTTTTAGTA[A/G]AGACAGGGTTTCACC | 81929 |
rs71353232 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949791 | GAATTCAGTGGCATA[A/G]AGCACAGCATTCACA | 81929 |
rs71370923 | in-del | -/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12981350 | TGGGGGGCCAAGGCA[-/G]GCAGCTGGGAGGTGG | 81929 |
rs71436628 | snp | C/G | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12979776 | CTGCCCAGCCAGCCG[C/G]CCCGTCCAGGAGGGA | 81929 |
rs72528947 | in-del | -/T/TT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986812 | CTTGTGTTTTTTTTT[-/T/TT]TCCTGTTTTTGTTTT | 81929 |
rs72636758 | snp | A/G | 0.23846 | 0.249734 | intron-variant | SEH1L | GRCh38.p7 | 18:12977946 | CCATCCTCCCACCTC[A/G]GCCTCCTGAGTAGCT | 81929 |
rs72874147 | snp | C/T | 0.437259 | 0.165632 | intron-variant | SEH1L | GRCh38.p7 | 18:12955065 | TAGGTGGGTATTTTC[C/T]GTAGAAAGAATTTGC | 81929 |
rs72874162 | snp | C/T | 0.104504 | 0.2033 | intron-variant | SEH1L | GRCh38.p7 | 18:12973591 | AGGTGTGAGCCACCA[C/T]GGCCGGCCTAGAAAT | 81929 |
rs72874177 | snp | A/T | 0.309648 | 0.24278 | downstream-variant-500B, utr-variant-3-prime | SEH1L | GRCh38.p7 | 18:12987661 | TAATAAAATATATTT[A/T]AAAATATACGAATCT | 81929 |
rs73407750 | snp | A/C | 0.118584 | 0.212673 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947197 | GGCCGCTTCCTTCCC[A/C]CGGGATGACACGTTT | 81929 |
rs73407763 | snp | G/T | 0.0191948 | 0.0960676 | intron-variant | SEH1L | GRCh38.p7 | 18:12951917 | GAAGGTTAGTATTTA[G/T]TTTTACATTTATTAA | 81929 |
rs73407884 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | SEH1L | GRCh38.p7 | 18:12954946 | CCCTGTGCTCATTTA[A/G]CAGTCACTTCTTGTT | 81929 |
rs73953324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12962826 | TGTGTGACAAAACTT[A/C]TTGTCTGAAAATTCT | 81929 |
rs73953326 | snp | C/G | 6.59207e-05 | 0.00574073 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984138 | TCAAATCCTTCCCTA[C/G]GTTCAACTATTCCAA | 81929 |
rs74256317 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972901 | TGTAGACATAAGCCC[A/C]AAAACGTAAAAGGTG | 81929 |
rs74352989 | snp | A/C/T | 1.65113e-05 | 0.00287322 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986981 | ATGCTGACACTGCCA[A/C/T]CCTCCAGTATCCTCA | 81929 |
rs74440160 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12965638 | ACTAGGTTTTATTAA[C/T]GAGCTGTCGTCAGTC | 81929 |
rs74623112 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964828 | ATTTTTAGTAGAGAC[A/G]GGGTTTGTCCATGTT | 81929 |
rs74922547 | snp | A/G | 0.444444 | 0.157135 | intron-variant | SEH1L | GRCh38.p7 | 18:12973962 | CCTAGAAGTATCTTA[A/G]CAGGCTTCTTATCAG | 81929 |
rs74979344 | snp | A/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12957441 | CTCAAAAAAAAAAAA[A/T]TACACTCTCCTTTAT | 81929 |
rs75038521 | snp | C/G | 0.039522 | 0.134904 | intron-variant | SEH1L | GRCh38.p7 | 18:12975437 | GATGGTCACCTGCTA[C/G]AGATGGCAGCACATA | 81929 |
rs75233261 | snp | G/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12962483 | TTTTTTTTTTTTTTT[G/T]TTGAGAGAGGGTCTT | 81929 |
rs75335027 | snp | A/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12950018 | TTTCACTTAGTATAA[A/T]TTTTTTTTTCTTTTT | 81929 |
rs75576434 | snp | A/T | 0.030278 | 0.119257 | intron-variant | SEH1L | GRCh38.p7 | 18:12950813 | TATATTTTTTCTGGG[A/T]AATAAGGTTTAATTT | 81929 |
rs75646889 | snp | C/T | 0.109461 | 0.206758 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986301 | TCATTCTGTGAATCC[C/T]TTTACTTATCAAAAT | 81929 |
rs75647569 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | SEH1L | GRCh38.p7 | 18:12972929 | GTGTATCATTGGCCA[C/T]GCGAGGTGACTTATG | 81929 |
rs75687303 | snp | G/T | 0.030278 | 0.119257 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946315 | TTTGGGTGATAATGA[G/T]GTGTCAATGTAGGTT | 81929 |
rs75879377 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SEH1L | GRCh38.p7 | 18:12984308 | ATGTTCACATGTGCT[C/T]GTATTAGCATTTAAG | 81929 |
rs75882156 | snp | C/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12966934 | GTATACATTTTTTCC[C/T]ATCATTGAATTTTTG | 81929 |
rs75903576 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | SEH1L | GRCh38.p7 | 18:12952218 | AACAAAACCTTTACT[C/G]AAGTAGAAATTTTCT | 81929 |
rs76305639 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SEH1L | GRCh38.p7 | 18:12977259 | CACCCAGTCTCCTAC[A/G]TGCAGGGGGTTAGGT | 81929 |
rs76454292 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | SEH1L | GRCh38.p7 | 18:12957744 | GCTATTACCCCTCAC[A/C]TGCCCTCCCTAATGG | 81929 |
rs76592190 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12977013 | CTGATTGTGTAGGCC[C/T]CAGGAGGGGGCTGAG | 81929 |
rs76690218 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | SEH1L | GRCh38.p7 | 18:12958844 | TTGAGACCGTGCTTT[C/T]GATTCTTTTGGAAAT | 81929 |
rs76802403 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12950530 | AGTTGTCATGGTAGA[A/G]TGTGTGTATATACGT | 81929 |
rs76966363 | snp | G/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12981878 | TTTTTTTTTTTTTTT[G/T]AGGCAAGGTCTCACT | 81929 |
rs76998264 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SEH1L | GRCh38.p7 | 18:12972534 | CAGATGGGCTTCGCA[A/G]GTACTAGACAAAATT | 81929 |
rs77021171 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SEH1L | GRCh38.p7 | 18:12968743 | GCTTTTGGAGGGAGG[C/T]GGAGATCCAGGTGAT | 81929 |
rs77174634 | snp | A/C | 0.0678174 | 0.1712 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946499 | AAAATCCACTGTTTC[A/C]CCTAATTCAACACTT | 81929 |
rs77406625 | in-del | -/C | 0.490563 | 0.0680388 | intron-variant | SEH1L | GRCh38.p7 | 18:12962221 | GGCAACATAGTGAGA[-/C]CCCCCCATCTCTATA | 81929 |
rs77514320 | snp | A/C | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12957428 | AGCGAGACTTCGTCT[A/C]AAAAAAAAAAAAATA | 81929 |
rs77679117 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986728 | TGAATATACTAAAGC[C/T]TTTTTTTTTTTTTCT | 81929 |
rs77679338 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | SEH1L | GRCh38.p7 | 18:12975384 | CATGGACTGTACTAA[G/T]AGCTGAAGGAGCTTA | 81929 |
rs77724135 | snp | C/T | 0.0569829 | 0.158885 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947377 | CCGAGCCTGGACTGC[C/T]TGTCATCCCCTCAGG | 81929 |
rs77750416 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957429 | GCGAGACTTCGTCTC[A/C/G]AAAAAAAAAAAATAC | 81929 |
rs77824661 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12972417 | AAGTTAATTTTGGTC[A/G]TGCCGAGATACAAGT | 81929 |
rs77908530 | snp | C/T | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949285 | ACAACTCCAGAGTAA[C/T]TGGAAATCTGAAGGA | 81929 |
rs78001413 | snp | G/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12955451 | TTTTCTTTTTTTTTT[G/T]TGATTCCCCAGACAC | 81929 |
rs78479727 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949197 | TAATGTGGGGATGCT[A/G]CATGAGATTTAGGAA | 81929 |
rs78526934 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SEH1L | GRCh38.p7 | 18:12985146 | TTGTAAATAGCTTCT[A/G]TTTTTTGATCTGTAT | 81929 |
rs78780289 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | SEH1L | GRCh38.p7 | 18:12975385 | ATGGACTGTACTAAG[A/T]GCTGAAGGAGCTTAC | 81929 |
rs78944617 | snp | A/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12950016 | TATTTCACTTAGTAT[A/T]ATTTTTTTTTTCTTT | 81929 |
rs79053934 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SEH1L | GRCh38.p7 | 18:12967312 | CATTGAACTCATAGC[C/T]AACAACACAAACTAC | 81929 |
rs79086071 | snp | C/T | 0.165853 | 0.235413 | intron-variant | SEH1L | GRCh38.p7 | 18:12966198 | CCTGGGTTTAAGAGA[C/T]TCTCCTGCCTCAGCC | 81929 |
rs79089316 | snp | C/T | 0.0130683 | 0.0797708 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971246 | TGAATATAATGAAAA[C/T]ACCAGGTCAGTCCTG | 81929 |
rs79167669 | snp | A/C | | | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987738 | GGCTTACTCTTCTTT[A/C]ACTATCTCACAAAAA | 81929 |
rs79241410 | snp | C/T | 0.110167 | 0.207236 | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12988004 | GGTTTAACCTCTTAT[C/T]AGGGCTAGAGAGAGA | 81929 |
rs79577542 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SEH1L | GRCh38.p7 | 18:12974925 | CTTTATTTACACTCT[C/T]ATTGAGGATCTTATT | 81929 |
rs79749565 | snp | C/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12964634 | ATTTACTCCCGTCTC[C/T]TTTTTTTTTTTTTTT | 81929 |
rs79766921 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12982408 | TGATGTGGTGGCGAG[A/T]CCACTTGTATTAATT | 81929 |
rs79825066 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | SEH1L | GRCh38.p7 | 18:12957163 | CCGGGTGCGGTGGCT[C/T]ACGCCTATAATCCCA | 81929 |
rs79896190 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SEH1L | GRCh38.p7 | 18:12962890 | TAAGAGAGATTACTT[A/G]TATAACAAAGGTAGG | 81929 |
rs79959182 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986729 | GAATATACTAAAGCT[C/T]TTTTTTTTTTTTCTA | 81929 |
rs80081342 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SEH1L | GRCh38.p7 | 18:12971096 | CAGTGTGTTCATTCT[A/G]TGAATGAAATGTGTA | 81929 |
rs80082998 | snp | C/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12964633 | TATTTACTCCCGTCT[C/T]TTTTTTTTTTTTTTT | 81929 |
rs80108323 | snp | A/G | 0.101301 | 0.200969 | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987340 | CAAAGTGCCTGTTCT[A/G]TAAATTTTATTTTAA | 81929 |
rs80161796 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | SEH1L | GRCh38.p7 | 18:12954400 | TGTTATCGATAGACT[A/G]TATTGTCAGTTAAAA | 81929 |
rs80253766 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SEH1L | GRCh38.p7 | 18:12953420 | TTTCTAAGAAACTGC[A/G]AAACTCTTCCAAAGT | 81929 |
rs111288711 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986174 | TTTAAATTAATTCAT[C/G]TCCTGTAAAGTTCTG | 81929 |
rs111405259 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12951525 | CCTCCCTAGTAGCTG[A/G]GACTATAGGCATGCG | 81929 |
rs111490972 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12958583 | TTGACTAGGTACTGC[A/G]TGTAAGTGGAATCAC | 81929 |
rs111526225 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12959533 | GTATGCTTCAATAAG[C/T]ATTTTCTTTGAGCAT | 81929 |
rs111547911 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12974570 | GGTGTGAGCCACCAC[A/G]CCCGGCCTGTTTATC | 81929 |
rs111577496 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12972467 | GCCAAAAGCAGTGTC[C/T]CAGAGGCACACTACT | 81929 |
rs111723530 | snp | C/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12978484 | AGAATACTTACTGCA[C/T]GTTGGATTTAGGACC | 81929 |
rs111734021 | in-del | -/A | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12957067 | CAAAAAAAAAAAAAA[-/A]TTCTATAAAAATTGT | 81929 |
rs111790249 | snp | A/G | 0.067446 | 0.170804 | intron-variant | SEH1L | GRCh38.p7 | 18:12955342 | CTCTCATAGAAGTAA[A/G]ACTATATTCTGTTTC | 81929 |
rs111793496 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12967227 | ACTACATTTTTGTCA[A/G]CTGATCAGTGTATAA | 81929 |
rs111817647 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SEH1L | GRCh38.p7 | 18:12957049 | CTCCAGCCTGGGCGA[C/T]GGAGCGAGACTTGTC | 81929 |
rs111834714 | snp | A/G/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12960762 | CTTTGAATTTCAAGA[A/G/T]ACTTATTTGTATTTA | 81929 |
rs111836460 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12975456 | TGGCAGCACATACCT[A/G]CCTGGTAGGGTGAGA | 81929 |
rs111966976 | in-del | -/CT | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986742 | CTTTTTTTTTTTTTT[-/CT]AGCATGTGTTTTCTC | 81929 |
rs112042439 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SEH1L | GRCh38.p7 | 18:12965035 | TTTTTTTTTTTTGAG[G/T]TGGAGTCTCGCTCTG | 81929 |
rs112243530 | snp | C/T | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946943 | CCTCATTTTTTTTTT[C/T]TCTGTACTTTCGCTC | 81929 |
rs112254211 | in-del | -/T | 0.211819 | 0.247067 | intron-variant | SEH1L | GRCh38.p7 | 18:12956007 | CTAACTCTAAAATTC[-/T]TTTTTTTTTTTAACT | 81929 |
rs112302826 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12965077 | GGAGTGCAGTGGCGC[A/G]ATCTAGGCTCACTGC | 81929 |
rs112317407 | snp | C/T | 0.464203 | 0.128908 | intron-variant | SEH1L | GRCh38.p7 | 18:12980843 | CCCCCACTTCCCTTC[C/T]GGACGGGGCGGCTGG | 81929 |
rs112381580 | snp | A/G | 0.106987 | 0.205054 | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987244 | ATCAAAGGAACATTT[A/G]CTTCACTGGGTGATA | 81929 |
rs112386420 | snp | A/C | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12950797 | CCTTCTTATTGTAAT[A/C]TATATTTTTTCTGGG | 81929 |
rs112389527 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | SEH1L | GRCh38.p7 | 18:12957421 | GAACAAGAGCGAGAC[G/T]TCGTCTCAAAAAAAA | 81929 |
rs112516463 | in-del | -/CCCC | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12969212 | AAAACTCTGTACCCG[-/CCCC]CCCCCCCCCCCCCAC | 81929 |
rs112707857 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12954525 | AGGCTGGAGTGCAGT[A/G]GCACAATCTTGGCTT | 81929 |
rs112715613 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SEH1L | GRCh38.p7 | 18:12976250 | GGCAGCTGCTTCTGC[A/G]AGGCCTGAAAGCAGG | 81929 |
rs112757623 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SEH1L | GRCh38.p7 | 18:12974256 | GGACTATGTAGTATC[A/G]TTATTAATACCTGTT | 81929 |
rs112863665 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SEH1L | GRCh38.p7 | 18:12957383 | TGATGAGCAGAGATC[A/G]TGCCATTGCACTCCA | 81929 |
rs112912312 | snp | A/C | 0.0111196 | 0.0737302 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947037 | TTCCTGATAAGCAAA[A/C]CCCCCCGAGTCGTTG | 81929 |
rs112957562 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12967662 | CTCACGCCTGTTATC[C/T]CAGCACTTTGGGAGG | 81929 |
rs113061602 | snp | C/T | 0.0629771 | 0.165899 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949748 | GTGAGCCACCGCGCC[C/T]GGCCCACGTTAACCG | 81929 |
rs113223090 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SEH1L | GRCh38.p7 | 18:12973456 | AAGTGCGTGCCACCA[C/T]GCCTGGCTAATTTTT | 81929 |
rs113225357 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12982752 | AATGTAAACTCTGAA[A/G]TATTTTTTGAAAATG | 81929 |
rs113297283 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12954466 | TTGTTAGACTTTTGA[A/G]GCAAATAATTTTTTT | 81929 |
rs113310554 | snp | C/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12956105 | GCTGGAGTGCAGTGG[C/T]ACAATCTTGGCTCAC | 81929 |
rs113341624 | snp | A/C/G | 0.0197687 | 0.0974348 | intron-variant | SEH1L | GRCh38.p7 | 18:12958201 | CGATTTTCCTGCCTC[A/C/G]GTCTCCTGAGTAGCT | 81929 |
rs113419170 | snp | C/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12983941 | AGCTCATAGCCTCTG[C/T]CTCGTTTCTTTAATT | 81929 |
rs113470857 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12968335 | CAACTGACAAAGCAA[A/G]AAAGATTTTCCGTTG | 81929 |
rs113502922 | snp | A/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12960242 | CATTATATTGTGGCA[A/G]CAAGGGATATTCAGC | 81929 |
rs113503350 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948848 | AGCAGAATTTCTTTT[C/T]TTTTTTTTTTTTTTT | 81929 |
rs113612669 | snp | A/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12951991 | TTGTTTTGAGAAAAT[A/T]ACATTTATACAGTAG | 81929 |
rs113624477 | in-del | -/T | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12954641 | CTGACTAATTTTTTG[-/T]ATTTTTTGTAGTGAT | 81929 |
rs113690982 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987292 | ATATGTCCAAGTAAC[A/G]TTAACTGTGAAGTTA | 81929 |
rs113713245 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12982335 | AAATGAAAATGACAT[A/T]GGCCCAGCTCAAGGG | 81929 |
rs113784266 | in-del | -/T/TT/TTT | 0.607895 | 0.163892 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986803 | TCTCTTTTTCTTGTG[-/T/TT/TTT]TTTTTTTTTTCCTGT | 81929 |
rs113792015 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SEH1L | GRCh38.p7 | 18:12955273 | TGTCTTCTAAAGGTT[A/G]AAACATTCTGGAATT | 81929 |
rs113792535 | snp | C/G | 0.5 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12974763 | TATGTGTGTTATGAA[C/G]TTTGAATCCTACCAA | 81929 |
rs113805588 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986028 | TGTTATTTATTCCAT[G/T]GCTTAGCTTCCTTCA | 81929 |
rs113814738 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SEH1L | GRCh38.p7 | 18:12956234 | CATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGC | 81929 |
rs113824344 | snp | C/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12970406 | CACTTTTCCCCTGTC[C/T]ATCTGTTTTTTCTTC | 81929 |
rs113860348 | snp | C/T | 0.242201 | 0.249878 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949018 | CCACCCCCGGCTAAT[C/T]TTTTTTTTTTTTTGT | 81929 |
rs113967767 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SEH1L | GRCh38.p7 | 18:12956843 | GCAAATTCTTTCTAC[A/G]GAAAATACCCACCTA | 81929 |
rs114127185 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949756 | CCGCGCCCGGCCCAC[A/G]TTAACCGTTTTAAAG | 81929 |
rs114151153 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12961787 | TTCTCCTGCCTTAGC[C/G]TCTCTAGTAGCTGGG | 81929 |
rs114172110 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SEH1L | GRCh38.p7 | 18:12960555 | ATTCAGACTGTTTTA[C/T]AGCTCTTCTCAGGGG | 81929 |
rs114273038 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SEH1L | GRCh38.p7 | 18:12952039 | CATTTTACTGTTTTT[C/T]GCTATTAAAGTAACA | 81929 |
rs114311318 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | SEH1L | GRCh38.p7 | 18:12957445 | AAAAAAAAAAAATAC[A/G]CTCTCCTTTATCTAC | 81929 |
rs114440210 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SEH1L | GRCh38.p7 | 18:12974067 | TTCAGCATCAAAAAC[A/G]AGGGGAAGTGGTGTT | 81929 |
rs114646603 | snp | A/T | 0.114146 | 0.209866 | intron-variant | SEH1L | GRCh38.p7 | 18:12962388 | CTAAGAAAAAAAAAA[A/T]AATAATAATAATAGT | 81929 |
rs114658754 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12961540 | TAATTATTCAGTGGT[A/G]TCTGTAGACAAAAGT | 81929 |
rs114699101 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12953926 | CAGTTTCCATTTTAT[A/T]GTGATGAGCATCTTT | 81929 |
rs114723263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12958409 | CTATTTGTAAATGGT[A/G]TAATTCAGTAGAATT | 81929 |
rs114800705 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SEH1L | GRCh38.p7 | 18:12952381 | GGGACTGTAGGCGTG[C/T]ACCACGATGCCCGGC | 81929 |
rs115089753 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | SEH1L | GRCh38.p7 | 18:12960990 | GAGGGCCAAGTGGGT[A/G]ACTTGAGAGAGTCAA | 81929 |
rs115142291 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12969908 | AAAACAGGAAAAAAA[C/T]GCAAAAGGAAGTTTG | 81929 |
rs115205390 | snp | A/T | 0.0127568 | 0.0788395 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986820 | TTTTTTTTTCCTGTT[A/T]TTGTTTTGTTTGGTG | 81929 |
rs115288645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961815 | GGGATTGCAGGCGCC[C/T]GCCACAATGTCTGGC | 81929 |
rs115328145 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | SEH1L | GRCh38.p7 | 18:12963915 | ATGGGGTTTTACCAT[A/G]TTGGCCAGACTGGTC | 81929 |
rs115335158 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SEH1L | GRCh38.p7 | 18:12968685 | TGGCACTCTTTCTAG[A/T]TTTCTAGCCCTGTAC | 81929 |
rs115625572 | snp | A/C | 0.0111196 | 0.0737302 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947712 | GTAGGGCATGACGGG[A/C]CGGGGGCGGGACGAG | 81929 |
rs115716409 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SEH1L | GRCh38.p7 | 18:12975352 | AAAATCTCACTTTTT[C/T]AACATTTCATAAGCA | 81929 |
rs115759752 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12970276 | CAGCTTATAGTTCAG[A/G]AGAGCCATTCTTTCA | 81929 |
rs115919193 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SEH1L | GRCh38.p7 | 18:12962717 | AGCTCAAGCAGTCTG[C/T]CTGCCTCGGCTTCCC | 81929 |
rs116077553 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SEH1L | GRCh38.p7 | 18:12978998 | TGGTTTATATTTCTG[C/T]TCTGGAAGTTTTACT | 81929 |
rs116101985 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | SEH1L | GRCh38.p7 | 18:12972499 | AGTCTTACAGGAGAA[A/G]AGAGCACTTGTCAGG | 81929 |
rs116252648 | snp | A/C | 0.0178098 | 0.0926698 | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987754 | ACTATCTCACAAAAA[A/C]CCCAAACAAAAATTA | 81929 |
rs116272221 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12976554 | CAGCATGTGTGCTCT[C/T]AGCTCCACCTGTCCT | 81929 |
rs116509075 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12957576 | AACATTGAACTAGAT[G/T]ATATTTAAGACTCTT | 81929 |
rs116599794 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SEH1L | GRCh38.p7 | 18:12960391 | GACCATTCTTTCCCC[C/T]GTTGAATGGTCTTGA | 81929 |
rs116654576 | snp | C/T | 0.110519 | 0.207473 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986741 | GCTTTTTTTTTTTTT[C/T]CTAGCATGTGTTTTC | 81929 |
rs116792109 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | SEH1L | GRCh38.p7 | 18:12978617 | ACATATTCTTTTGGG[A/G]GCTGCTGTTGAGCCC | 81929 |
rs116807153 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SEH1L | GRCh38.p7 | 18:12958393 | GCCTGGCCCATTTTA[A/G]CTATTTGTAAATGGT | 81929 |
rs116828909 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12953224 | TGATACTGAGTAGTC[C/T]GTTGTATGTATATTG | 81929 |
rs116884204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12972238 | GGATCTGGTGATTGA[C/T]TGGATTTGAGAACTG | 81929 |
rs117133556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949785 | AGTGTAGAATTCAGT[A/G]GCATAGAGCACAGCA | 81929 |
rs117231205 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SEH1L | GRCh38.p7 | 18:12970190 | TGCCAGGTTTACAGA[A/G]ATATTAATTAATCTG | 81929 |
rs117307220 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SEH1L | GRCh38.p7 | 18:12959814 | TGAAGACTTTCCCCA[A/G]TGTTTTCTTCTAAGA | 81929 |
rs117403554 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12984362 | TTGGCTTACTTGGTC[A/T]TAATATTTGCAGGTA | 81929 |
rs117549164 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | SEH1L | GRCh38.p7 | 18:12952002 | AAATAACATTTATAC[A/T]GTAGTTCTTTTCCTG | 81929 |
rs117568712 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12976638 | GATTTAGGAATTATT[A/G]GTTTATAGGTACTGA | 81929 |
rs117606295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961601 | AATATTATCCTTTTA[A/G]TGTTGAGACTCTTTA | 81929 |
rs117621211 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SEH1L | GRCh38.p7 | 18:12972131 | TGCTATGAAGACAGT[C/T]CAGGTGGGAGAGTAC | 81929 |
rs117651768 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947600 | TTGCACAGTATACCA[A/G]TAAGCTCTTACTACT | 81929 |
rs117889884 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SEH1L | GRCh38.p7 | 18:12952758 | CTCCCTCTCCCCTCC[C/T]CTCCCACCCTCTCTT | 81929 |
rs117928661 | snp | G/T | 0.039522 | 0.134904 | intron-variant | SEH1L | GRCh38.p7 | 18:12957526 | GAACATAATATAATC[G/T]GTGTGCTGTTGAAGT | 81929 |
rs117978838 | snp | A/G | 0.0280468 | 0.115051 | missense, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12951879 | AAAAGTGAAAGTGGT[A/G]ATTGGCATTGTACTG | 81929 |
rs118042246 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985713 | GAATAAATATTTTTT[A/G]TAAAGATTGTTTTGA | 81929 |
rs118060189 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946520 | TTCAACACTTCACTC[C/T]CACTCTGATAATCTC | 81929 |
rs118101711 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12952393 | GTGCACCACGATGCC[C/T]GGCTAATTTTTGTGT | 81929 |
rs137918111 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946657 | TAGTGAGCACTTTCT[C/T]TGGAAATGAGTGTCT | 81929 |
rs138005192 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12975803 | GTAGCCCACTATGAT[G/T]TGGAATGAGGACATG | 81929 |
rs138137924 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SEH1L | GRCh38.p7 | 18:12967252 | GTATAACCTTTTTGT[G/T]TGTCTTTCTTTTTAA | 81929 |
rs138176288 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SEH1L | GRCh38.p7 | 18:12950238 | GCAGGGTCTTGCTGC[A/G]TTGCCCAGGCTAGTC | 81929 |
rs138190378 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12954586 | ATCCTCCCACCTCAG[C/G]CTCCCAAGCAGCTGG | 81929 |
rs138459666 | snp | C/T | 0.00839921 | 0.0642578 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971180 | TTCCCCCATGATCGC[C/T]GTAGGAAGTGATGAC | 81929 |
rs138518398 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976316 | GTGTTGTAGTCACAC[A/G]GGTGTTGTCCCACCA | 81929 |
rs138590778 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12978002 | CCAGCTATTTCTGTA[-/T]TTTTTTGTAAAGATG | 81929 |
rs138623178 | snp | C/T | 0.000182978 | 0.00956324 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987034 | CGGCCTCTTAATCCC[C/T]TACCTGAGAATGAAG | 81929 |
rs138673189 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947033 | CCTTTTCCTGATAAG[C/G]AAAACCCCCCGAGTC | 81929 |
rs138726079 | snp | C/G | 0.000299431 | 0.0122322 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986918 | GATGGTCCAGTTATG[C/G]CCAGCTCCTTCCTCC | 81929 |
rs138765210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12968104 | CTTGTTTTTCTTGGG[C/T]GTCTGCTGATCTTTG | 81929 |
rs138800135 | snp | C/T | 0.039522 | 0.134904 | intron-variant | SEH1L | GRCh38.p7 | 18:12957280 | TAAAAATACAAAAAT[C/T]AGCTGAGCATGGTGG | 81929 |
rs138814726 | snp | A/C/T | 0.0279689 | 0.115005 | intron-variant | SEH1L | GRCh38.p7 | 18:12953485 | TTCTCTACATCCTCA[A/C/T]CTACACTCGATAATA | 81929 |
rs138934038 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965010 | CCATTTCCTCATTCT[-/T]TTTTTTTTTTTTTTT | 81929 |
rs138946615 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | SEH1L | GRCh38.p7 | 18:12970610 | ATTTTTTTTTTGTAG[A/C]GATAGAGTCTTATTA | 81929 |
rs139191978 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12950976 | ACAGGTGTGCACCAC[C/T]ATGCCTGGTTTCAAT | 81929 |
rs139329981 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12973148 | GGGAGGTCGAGGCTG[C/T]GGTAAATCAAAATTG | 81929 |
rs139368225 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SEH1L | GRCh38.p7 | 18:12977093 | AGCAAGGATGTGGAT[G/T]AGATTGCTTAGGGTG | 81929 |
rs139432256 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948740 | GAAGAAAAATACAAA[C/G]CATTTACATCCAATG | 81929 |
rs139733316 | snp | C/T | 0.00014912 | 0.00863353 | missense, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948147 | CTCGCAGCATCGCGG[C/T]GGACCACAAGGATCT | 81929 |
rs139734049 | in-del | -/TTT | 0.00716266 | 0.059414 | intron-variant | SEH1L | GRCh38.p7 | 18:12965849 | GTTTTATTTGAGCAG[-/TTT]TTTCCACCTTGGGGT | 81929 |
rs139859888 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SEH1L | GRCh38.p7 | 18:12963964 | GTGATCTGCCTGCCT[C/T]GGCCTCCAAGAGTGC | 81929 |
rs140019942 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SEH1L | GRCh38.p7 | 18:12984676 | AGAGGAAATAATAAA[A/G]CACGAGATTGATTTT | 81929 |
rs140150049 | snp | C/T | 0.000300541 | 0.0122548 | intron-variant | SEH1L | GRCh38.p7 | 18:12955638 | TAGTATTCTGGGGAC[C/T]GGGAAGACATGAGCA | 81929 |
rs140156926 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12951624 | TCGAACTCCTGACCT[C/G]AGGTGATCCGTTTGC | 81929 |
rs140193247 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978762 | ATTAGGAAATATGCA[A/G]AAGCTGAAACTCTTA | 81929 |
rs140201819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12954978 | ACTCTGCTCCCAGCC[G/T]CTGGTAACCACTAAT | 81929 |
rs140218685 | snp | A/G | 0.0033222 | 0.0406209 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12955480 | ACATAGTGGATCTGT[A/G]TGGCGTGTGACATGG | 81929 |
rs140288468 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986448 | AAAAAAAATGTGTGC[C/T]TGCTGCTGCTGTGAG | 81929 |
rs140302471 | snp | C/T | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971157 | CCCGTTTCTAGCTCT[C/T]GTGCTCATTCCCCCA | 81929 |
rs140307782 | snp | C/G | 0 | 0 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946078 | AGCCACTCCAAGATT[C/G]CCATTATATGCCATT | 81929 |
rs140359077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12965332 | CCTAATTCTTATATT[G/T]CTTGTATACTGGCAA | 81929 |
rs140391404 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | SEH1L | GRCh38.p7 | 18:12958600 | GTAAGTGGAATCACA[G/T]TATTTGTCCATTTGC | 81929 |
rs140609812 | in-del | -/TAGTA | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12950010 | TTGGTTTATTTCACT[-/TAGTA]TAATTTTTTTTTTCT | 81929 |
rs140610410 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SEH1L | GRCh38.p7 | 18:12967128 | CACTGGCAATGTTCT[A/G]TAAAGTTGCCATGAA | 81929 |
rs140630364 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | SEH1L | GRCh38.p7 | 18:12969765 | GGTGTGGTGGTTCAC[A/G]CCTGTAATCCCAGCT | 81929 |
rs140675812 | snp | A/C | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986629 | TAACAGATTGTATTC[A/C]TTTCAAGTTTCTATA | 81929 |
rs140689908 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime | SEH1L | GRCh38.p7 | 18:12987552 | TGTGGACTTTTTGGT[-/C]TTTTTTTTTTTTTTT | 81929 |
rs140938225 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | SEH1L | GRCh38.p7 | 18:12952377 | AGCTGGGACTGTAGG[C/T]GTGCACCACGATGCC | 81929 |
rs140945309 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12970247 | TAATTAGGCATAGAA[A/G]TTAAAAAGTCATTCA | 81929 |
rs141033327 | in-del | -/A | 0.165527 | 0.235296 | intron-variant | SEH1L | GRCh38.p7 | 18:12969889 | GCAAGGCTCTGTCTC[-/A]AAAAAAACAGGAAAA | 81929 |
rs141239172 | snp | G/T | 0.00518109 | 0.0506754 | intron-variant | SEH1L | GRCh38.p7 | 18:12982451 | TGTGTATATATATAT[G/T]TGTGTGTATATATAT | 81929 |
rs141361510 | snp | C/T | 0.0599851 | 0.162463 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949087 | GCTGGTCTCGAACTC[C/T]TGACCTCGTGATCCA | 81929 |
rs141375482 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SEH1L | GRCh38.p7 | 18:12949999 | CCCTTTTATATTTGG[C/T]TTATTTCACTTAGTA | 81929 |
rs141503169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12976578 | CTGTCCTATTTCTGG[C/T]CTTTGGTAGAAGGCC | 81929 |
rs141629073 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SEH1L | GRCh38.p7 | 18:12971794 | ATCTGGTTTAGGGGC[C/T]AGGAAGGTTCACCTA | 81929 |
rs141736699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12977248 | GGAGATGTCTCCACC[C/T]AGTCTCCTACATGCA | 81929 |
rs141847263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12970655 | TTCTTGAACTCCTGG[C/T]CTCAAATGATCCTCT | 81929 |
rs141888007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12974599 | TCTTTTTCTAAGTAG[C/T]ATCACCATTTAGTAG | 81929 |
rs142005060 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SEH1L | GRCh38.p7 | 18:12962880 | TCAGTTTGCTTAAGA[A/G]AGATTACTTATATAA | 81929 |
rs142041554 | snp | C/T | 0.00939562 | 0.0678935 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971216 | CCCCAACGCAATGGC[C/T]AAGGTTCAGATTTTT | 81929 |
rs142273378 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12953075 | GCTTGAGCCACCATG[C/G]CTGGCCTGGTTTATC | 81929 |
rs142298347 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SEH1L | GRCh38.p7 | 18:12974501 | GCCAGGATGGTCTCC[A/G]TCTCTTGATCTTGTG | 81929 |
rs142362008 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946692 | CCTTCAAAAAAGTTA[C/T]AGTTGTTATCAGTTA | 81929 |
rs142668026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12966075 | CACTTACCATTTGTT[C/T]TTTATTTTTATTTTT | 81929 |
rs142743819 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SEH1L | GRCh38.p7 | 18:12968866 | AGTTCTGGTTGTACA[A/G]TTGAGGTAATCCTCA | 81929 |
rs142773894 | snp | A/C/G | 8.25411e-05 | 0.00642378 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986965 | GTAGAGCACTCTTGC[A/C/G]ATGCTGACACTGCCA | 81929 |
rs142805702 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987775 | ACAAAAATTAGGAGA[G/T]GTGAGCAAATATTAC | 81929 |
rs142860858 | snp | C/G | 0.114387 | 0.210022 | intron-variant | SEH1L | GRCh38.p7 | 18:12969811 | ACAGGAGAATCACTT[C/G]AACCCAGGAGGTGGA | 81929 |
rs143047266 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12975996 | CATATGTTTGAGGTG[C/T]GTTTGGAACATCCAG | 81929 |
rs143101349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12951396 | CATTCAAGGTTCTCA[A/G]TGTAAATTTTTTGAG | 81929 |
rs143183668 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | SEH1L | GRCh38.p7 | 18:12965075 | CTGGAGTGCAGTGGC[A/G]CAATCTAGGCTCACT | 81929 |
rs143221709 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SEH1L | GRCh38.p7 | 18:12967796 | GTGTGCGCCTGTACT[C/T]CCAGCTACTCAGGAG | 81929 |
rs143231376 | snp | C/T | 0.000215141 | 0.0103694 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987019 | AGACGATATCTCTCT[C/T]GGCCTCTTAATCCCT | 81929 |
rs143361838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978469 | TTCTCTTCTTTTTAA[A/C]GAATACTTACTGCAC | 81929 |
rs143405295 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12967698 | GCGGGCGGATCACTT[C/G]AAGTCAGGAGTTTGA | 81929 |
rs143426358 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SEH1L | GRCh38.p7 | 18:12952942 | GCATGCCACCACACC[C/T]GGCTAATTTTTGTAG | 81929 |
rs143470021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12972580 | CAGATCTTAGGCAGG[A/G]CCAGCAGTAGAGAAG | 81929 |
rs143526067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12956931 | AATTAGCCCGGCATG[A/G]TGGTGGGTGCCTGTA | 81929 |
rs143640963 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SEH1L | GRCh38.p7 | 18:12950841 | TTTTTTTGTTTTGAG[A/G]TGGAGTCTTGCCATG | 81929 |
rs143847623 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SEH1L | GRCh38.p7 | 18:12951793 | ACTGATTCAGTCTTA[C/T]AGTTTTTGTATCAAT | 81929 |
rs143962546 | snp | C/T | 8.23649e-05 | 0.00641683 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971207 | TGACAGTAGCCCCAA[C/T]GCAATGGCCAAGGTT | 81929 |
rs144250729 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12965435 | TCTAAAAATTAAGTG[G/T]CAGCCAGCTTTACAA | 81929 |
rs144359540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985994 | AATGTTTCTTATATA[C/T]ATTTGTGTATTTTTA | 81929 |
rs144565252 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947457 | CCTGACCAAACCCAC[C/G]GTTCGTCTTCTCCAC | 81929 |
rs144622552 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948375 | CCTGGCTGGACTGAG[C/T]GGAAGCCCTCCCCGC | 81929 |
rs144697552 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12951428 | CGGAGTCTTGCTTTG[C/T]CTCCCAGGCTGGAGT | 81929 |
rs144704738 | in-del | -/G | 0.0170251 | 0.090679 | intron-variant | SEH1L | GRCh38.p7 | 18:12975648 | ATTTTGGAGAGTGGT[-/G]GCTTGCCAAGTCTGA | 81929 |
rs144730855 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SEH1L | GRCh38.p7 | 18:12966497 | CCTCCCTGGGCTCAG[A/G]TGATCCTCCCACCAC | 81929 |
rs144993255 | snp | A/C/G | 6.59158e-05 | 0.00574059 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984098 | TAATGGGAGCCCAGT[A/C/G]AATGGGAGTTCTCAG | 81929 |
rs145064996 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12961715 | ACTGCCACCCAGCCT[A/G]GTGTGCAGTGGCATG | 81929 |
rs145087231 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949194 | TTCTAATGTGGGGAT[G/T]CTACATGAGATTTAG | 81929 |
rs145193261 | snp | A/G | 0.143959 | 0.226396 | intron-variant | SEH1L | GRCh38.p7 | 18:12981110 | CTTCTCAGACAGGGC[A/G]GCCGGGCAGAGATGC | 81929 |
rs145253657 | in-del | -/CATTC | 0.0166325 | 0.0896639 | intron-variant | SEH1L | GRCh38.p7 | 18:12984712 | ATTTAGCATATGTTA[-/CATTC]CATTCTTGTATATCA | 81929 |
rs145288849 | snp | A/C | 0.0444908 | 0.142359 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986491 | TAAGATAAAAAACTT[A/C]ACTAGATCTGTAAAT | 81929 |
rs145324977 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946210 | CAAACTATTCCGCGT[A/G]ATACTATAATGGTGG | 81929 |
rs145327380 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12978196 | TATTAAAGGAGGAAA[C/T]GTGGGAGGTTGTATT | 81929 |
rs145455643 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965646 | TTATTAACGAGCTGT[C/T]GTCAGTCTGATGCTG | 81929 |
rs145496300 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | SEH1L | GRCh38.p7 | 18:12952503 | CCAAAGTGCTGGGTT[C/T]ATAGGCATGAGCCAC | 81929 |
rs145612355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12962569 | GCCCCACTGGCTCAA[A/G]CGATCCACCCGCCTC | 81929 |
rs145661782 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967140 | TCTATAAAGTTGCCA[G/T]GAACACTGAATTAGC | 81929 |
rs145679761 | snp | A/G | 0.000462 | 0.0151917 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12955588 | AGAATCAAATGATAA[A/G]CTGCGAGGACAGAGC | 81929 |
rs145852229 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985420 | CTTTAAAAATACAGT[A/G]TATATTTTTTGTACT | 81929 |
rs146042185 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SEH1L | GRCh38.p7 | 18:12953454 | TGTGCCCACCAGCCA[C/T]GTGTGAGGTTCCAGT | 81929 |
rs146251836 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12972584 | TCTTAGGCAGGGCCA[A/G]CAGTAGAGAAGGAAC | 81929 |
rs146278290 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SEH1L | GRCh38.p7 | 18:12976924 | GAGCTTGCAGTGAGC[C/T]GAGATCACACCACTG | 81929 |
rs146696286 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986268 | ACAAGATGGAAGAAG[A/G]ATAACAGTAGGGCAC | 81929 |
rs146723981 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12969629 | GGAGATGGAGGTTGC[A/T]GTAAACCAAGATCAT | 81929 |
rs146815628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12966715 | CCAATCCTGCTTGAC[A/G]CTCAGTGGTCCCTTT | 81929 |
rs146844002 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SEH1L | GRCh38.p7 | 18:12952286 | TGCCCAGGTGGGAGT[G/T]CAGTGGCGTGATCTT | 81929 |
rs147097098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12970927 | TGAGCCATAAGAATA[C/T]GCTAAAAACAGTTCA | 81929 |
rs147119478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12975078 | GCTCACCGTAACCTC[C/T]GCCCCCTGGGTTCAA | 81929 |
rs147170727 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SEH1L | GRCh38.p7 | 18:12965202 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTAT | 81929 |
rs147180997 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SEH1L | GRCh38.p7 | 18:12950876 | CCAGGCTGGAGTGCA[C/G]TGGCTATTCACGGGC | 81929 |
rs147242511 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | SEH1L | GRCh38.p7 | 18:12984535 | CATTAGTGTTTTTTA[C/G]TGCTTGTAGTGTGGT | 81929 |
rs147277460 | snp | G/T | 0.118584 | 0.212673 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948048 | GCTGCGAGGTCTGGC[G/T]AGGCTACGGGCCACG | 81929 |
rs147367695 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956049 | AGGGTTAATAAAATT[-/C]TTTTTTTTTTTTTTA | 81929 |
rs147485672 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SEH1L | GRCh38.p7 | 18:12982463 | TATGTGTGTGTATAT[A/G]TATATGTTTTAAAAC | 81929 |
rs147497340 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SEH1L | GRCh38.p7 | 18:12967817 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 81929 |
rs147560381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12955942 | TCTCAAACTCCTGGC[C/T]CCACCTCAGCCTCCT | 81929 |
rs147570181 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SEH1L | GRCh38.p7 | 18:12958169 | GCTTACTGCATTCTC[C/T]GCCTCCGGGGTTCAA | 81929 |
rs147736172 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12975119 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATCACA | 81929 |
rs147738564 | snp | A/G | | | splice-acceptor-variant | SEH1L | GRCh38.p7 | 18:12963158 | TATTATTTTTTTTTT[A/G]GGTTAAAAGGACAAC | 81929 |
rs147745727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978364 | TAGTCCAGCTCCTGC[C/T]GGCTCCGGGAGTTCT | 81929 |
rs147852860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12958531 | GCCTCCCCCTTCCTC[C/T]TCCCTCTACCCCCTA | 81929 |
rs147872432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12974573 | GTGAGCCACCACGCC[C/T]GGCCTGTTTATCTTT | 81929 |
rs147975103 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986523 | TACAGAATAGCATCA[C/G]ATGTTTCTGAGAGAT | 81929 |
rs148180393 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12962764 | AGGTGTAAGCCATCA[C/T]GCCCAACTCATTTAC | 81929 |
rs148189020 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949899 | CCTGTTCCGCCACCC[C/T]ATCCTCTGGTAACCT | 81929 |
rs148368192 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SEH1L | GRCh38.p7 | 18:12967786 | GGGCGTGGTGGTGTG[C/T]GCCTGTACTCCCAGC | 81929 |
rs148440474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12957989 | GCTGTGATTATAGGC[A/G]TGAGCCACTACGAGG | 81929 |
rs148490489 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SEH1L | GRCh38.p7 | 18:12965767 | TTATGATGGATTTTG[A/G]TAGCCAATGGAAATG | 81929 |
rs148731401 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12973882 | CTTATGATCACAAAA[G/T]AGCTGCACAATGTCA | 81929 |
rs148827356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12952680 | TGTATCCTATTCCCA[C/T]TCCAAGCCCCAGGCA | 81929 |
rs148985802 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985979 | GTCACTAAAGAGATA[A/C]ATGTTTCTTATATAC | 81929 |
rs149172109 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12961534 | TTGTATTAATTATTC[A/G]GTGGTGTCTGTAGAC | 81929 |
rs149216760 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SEH1L | GRCh38.p7 | 18:12978417 | CAATCTCTGCCTCTG[C/T]GTTCACATGGCTGCC | 81929 |
rs149321051 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947121 | CCAGGGGCTCTGGCC[C/T]TCTTCACTTCCTTTT | 81929 |
rs149468070 | in-del | -/A | 0.0876345 | 0.190099 | intron-variant | SEH1L | GRCh38.p7 | 18:12975330 | CTTGCCTCAGGTAAG[-/A]AAAAAAAAAATCTCA | 81929 |
rs149480857 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12975972 | GTGGTAAGCACAATT[C/T]ATTTCAGACATATGT | 81929 |
rs149534248 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SEH1L | GRCh38.p7 | 18:12981943 | TGGCTCACTGCAACC[C/T]CCACCTCCCAGGTTC | 81929 |
rs149563434 | snp | A/G | 0.0143705 | 0.0835389 | intron-variant | SEH1L | GRCh38.p7 | 18:12954642 | TGACTAATTTTTTGT[A/G]TTTTTTGTAGTGATG | 81929 |
rs149616269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957562 | ATCTATAAAGTGAAA[A/T]CATTGAACTAGATTA | 81929 |
rs149686293 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | SEH1L | GRCh38.p7 | 18:12952481 | CAGGTGATCCTCCCT[C/T]GGCCTCCCAAAGTGC | 81929 |
rs149713469 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949597 | AGCTGGGACTACAGG[C/G]GCCCGCCACCACGCC | 81929 |
rs149792580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12977655 | CTTGAACTCAGGAGG[C/T]GGAGGTTTCAGTGAG | 81929 |
rs149846400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12984975 | TCATAAAGAAGTTCT[A/G]CTTTTGATTTTGAGG | 81929 |
rs149868622 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12969428 | GGCATGGTTGTTTAC[A/G]CCTGTAATCCCAGCA | 81929 |
rs149891346 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12955916 | TTTTAAAGTATTCTG[G/T]CTCACTGCAGTCTCA | 81929 |
rs149922315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12973186 | TCACTCCAGCAGTGT[C/T]AAAAAAAGATTTTTT | 81929 |
rs150057875 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948742 | AGAAAAATACAAACC[A/G]TTTACATCCAATGAT | 81929 |
rs150075217 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946723 | TCATAAGAGGTGGGG[C/T]CCACCTCTTAAAGTA | 81929 |
rs150171090 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986700 | GTGCTATTATGTTCT[A/G]TTAGTTTTGGCATGA | 81929 |
rs150182644 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SEH1L | GRCh38.p7 | 18:12970447 | TTTTTCTGAAAGAGA[C/T]TCTCACTCTGTTGCC | 81929 |
rs150232659 | snp | A/G | | | intron-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12975798 | ATGCAGTAGCCCACT[A/G]TGATGTGGAATGAGG | 81929 |
rs150357610 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978812 | TCATGATATTGCATT[C/T]GCTCCAAATTTGGGA | 81929 |
rs150360561 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959516 | CAAAAACTTGAAATT[C/T]GGTATGCTTCAATAA | 81929 |
rs150381352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12950077 | CTGGCTCTGTCACCC[A/G]GGCTGGAGTGCAGTG | 81929 |
rs150466694 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953869 | AAGGCTTTTTATTAA[-/C]CAGCCAATAAATATA | 81929 |
rs150507996 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12972120 | CACGGCTAGGATGCT[A/G]TGAAGACAGTCCAGG | 81929 |
rs150561646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12977347 | TACCACTGCCTTCAT[G/T]ATCCTCTTATTCTGT | 81929 |
rs150676557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12963920 | GTTTTACCATGTTGG[C/T]CAGACTGGTCTTGAA | 81929 |
rs150695305 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SEH1L | GRCh38.p7 | 18:12951617 | GCTGGTCTCGAACTC[C/T]TGACCTCAGGTGATC | 81929 |
rs150857259 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SEH1L | GRCh38.p7 | 18:12954184 | TAAAAAATGTTAGCT[A/G]TACAGTGTGAAACAC | 81929 |
rs151055946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12969953 | TGCTGTGGAATTTAC[A/C]TCTATTTGAATGGCC | 81929 |
rs151247732 | snp | C/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948547 | GGGGCATCCCACCGT[C/T]AGCCTCGGCGTCGTG | 81929 |
rs151296974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978562 | AAGACGCTATTTTTG[A/C]ATAAGGTCACATTCA | 81929 |
rs180775460 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947138 | CTTCACTTCCTTTTC[C/T]CCGGAGGACTCTGGC | 81929 |
rs180780743 | snp | C/T | 0.237882 | 0.249706 | intron-variant | SEH1L | GRCh38.p7 | 18:12979863 | AATGGGGCGGCTGGC[C/T]GGGCGGGGGGCTGAC | 81929 |
rs180782385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12968005 | GTTTACAAGTGCAGA[A/G]TCTCTAAATAGTGAG | 81929 |
rs180828759 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SEH1L | GRCh38.p7 | 18:12957149 | TATACTGTCCTCGGC[C/T]GGGTGCGGTGGCTCA | 81929 |
rs180858612 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12973410 | GTTCAAGTGATTCTC[A/C]TGCCTTAGCCTCCTG | 81929 |
rs180926475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12973986 | TTATCAGGTGCTGGC[A/G]GCTGGAGTTTGGTCA | 81929 |
rs180944850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12953380 | GATGCGTAGGAGTGG[A/G]ATTGATGGGCTATAT | 81929 |
rs180964922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12984306 | AAATGTTCACATGTG[C/T]TTGTATTAGCATTTA | 81929 |
rs180992359 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SEH1L | GRCh38.p7 | 18:12961330 | GTTTCAGGTGTTTCT[A/G]TCTGTTGGGAGACTA | 81929 |
rs181112481 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | SEH1L | GRCh38.p7 | 18:12981036 | AGACGGTGTGGCTGC[C/T]GGGCGGAGGGGCTTC | 81929 |
rs181131439 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957571 | GTGAAAACATTGAAC[C/G/T]AGATTATATTTAAGA | 81929 |
rs181342219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12966338 | CTCAGGTGATTTGCC[A/G]GCCTCGGCCTCCCAA | 81929 |
rs181470652 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12984917 | CTATATAAAAGAAGA[A/C]AATTGTATTTAAAAT | 81929 |
rs181471714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961930 | CTCAGTCTCCCAAAG[A/T]GCTGGGATTACAGGC | 81929 |
rs181596209 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12981737 | CTATTTAGGGAAAAC[A/T]AAATTAGTATTGAGA | 81929 |
rs181937800 | snp | A/T | 3.29924e-05 | 0.00406142 | intron-variant | SEH1L | GRCh38.p7 | 18:12963385 | AGGTAAGTTTACATA[A/T]TAAACCTCTGATAAC | 81929 |
rs182043115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12952884 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 81929 |
rs182054620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12973213 | TTTTTCTAAAACATA[A/G]GAAAAGAAAATATTT | 81929 |
rs182058597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12967212 | TTCCACAAGTCTCTC[A/G]CTACATTTTTGTCAA | 81929 |
rs182183240 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SEH1L | GRCh38.p7 | 18:12970613 | TTTTTTTTGTAGAGA[C/T]AGAGTCTTATTATGT | 81929 |
rs182229201 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985757 | TACTTTTTGTAGATT[A/T]GCTTTATCCATGATA | 81929 |
rs182318226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12976490 | CCTCCCACTTTACGG[A/G]GAACTTGCTGAAGGT | 81929 |
rs182507434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12968878 | ACAATTGAGGTAATC[C/T]TCAATTCAGGTTGCT | 81929 |
rs182522794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948676 | CTCTCACCAGGGCAC[A/G]TGGTTTTCTCCGTGG | 81929 |
rs182565135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12981896 | GCAAGGTCTCACTCC[A/G]TTGCCCAGGCTGGAG | 81929 |
rs182705813 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986002 | TTATATACATTTGTG[C/T]ATTTTTATGGTGTTA | 81929 |
rs182717611 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SEH1L | GRCh38.p7 | 18:12955147 | AACTCTGAAGCAACT[C/T]TCCAACTATCAGCAC | 81929 |
rs182777485 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959203 | TAAATTGGGTTTTTT[A/G]TTGTTATAGGAGTTC | 81929 |
rs182850930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12958541 | TCCTCCTCCCTCTAC[C/T]CCCTATTCAACTGTC | 81929 |
rs182904559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12963914 | CATGGGGTTTTACCA[C/T]GTTGGCCAGACTGGT | 81929 |
rs182943497 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957925 | TGTTGCCCAGGCTGG[G/T]CTTGAACTCCTGGAC | 81929 |
rs183028647 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12964381 | ATGTTATCTTTTTTT[A/T]AAAAATTTTTATTCT | 81929 |
rs183078717 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12954580 | GAAGTGATCCTCCCA[C/T]CTCAGCCTCCCAAGC | 81929 |
rs183084167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12975956 | GCAAAGAGGAGTGAA[C/T]GTGGTAAGCACAATT | 81929 |
rs183158631 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SEH1L | GRCh38.p7 | 18:12982732 | GCTCTGCAATTTTTA[C/T]TTAAAATGTAAACTC | 81929 |
rs183413734 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SEH1L | GRCh38.p7 | 18:12975326 | TATAGCTTGCCTCAG[A/G]TAAGAAAAAAAAAAT | 81929 |
rs183494633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949106 | CCTCGTGATCCACCC[A/G]CCTCGGCGCCTCGGC | 81929 |
rs183577456 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SEH1L | GRCh38.p7 | 18:12954188 | AAATGTTAGCTATAC[A/G]GTGTGAAACACATTT | 81929 |
rs183594597 | snp | C/G/T | 0.0134995 | 0.0811632 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949719 | CGGCCTCCCAAAGTG[C/G/T]TAGGATTACGGGCGT | 81929 |
rs183731370 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965303 | AGGCATGAGCCACCT[C/T]GCCCAGTCCATTTCC | 81929 |
rs183806483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12969557 | GCTGGGCGTGGTGGC[A/G]CGTGCCTGTAATCCC | 81929 |
rs183862950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961520 | CTCAACATTTGTGTT[G/T]GTATTAATTATTCAG | 81929 |
rs183886059 | snp | C/T | 1.74821e-05 | 0.00295647 | intron-variant | SEH1L | GRCh38.p7 | 18:12971300 | AATTGCATTTAATTT[C/T]TTAAAATGTTATTTC | 81929 |
rs184006323 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12966381 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCACCAT | 81929 |
rs184470119 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987453 | TATGAGACCTTAAAA[A/T]ATGGATTTCATTTTA | 81929 |
rs184636323 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12982779 | AATGGTCTTTTACAG[C/T]TACTTTTAATGTCAT | 81929 |
rs184663762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12960311 | CTGATACAAATTATT[C/T]ATTTCAGTCATTAAA | 81929 |
rs184755465 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12984514 | GAGAGTTTTAGTCCA[A/T]ATGAACATTAGTGTT | 81929 |
rs184771046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978479 | TTTAAAGAATACTTA[C/T]TGCACGTTGGATTTA | 81929 |
rs184788260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12950771 | TACATTTTTAACAGG[C/T]GAAATTGGCACCTTC | 81929 |
rs184791957 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957083 | AAAAAAAAAAAAATT[A/C]TATAAAAATTGTTTC | 81929 |
rs185132509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12976876 | AGCTACTCCGGAGGC[C/T]GAGGCAGGAGAATGG | 81929 |
rs185235845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12956756 | TTCCAGTGCTGATAG[C/T]TGGAGAGTTGCTTCA | 81929 |
rs185294147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12951671 | GCTGGGATTACAGGC[A/G]TGAGCCATCGCACCC | 81929 |
rs185401639 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972095 | GTTTTGGAGGGAAAC[A/G]TGGTGGATTCACGGC | 81929 |
rs185448081 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12964981 | GTTTATTGCTTCCCC[C/T]TCACATTGCCCCTTC | 81929 |
rs185484630 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947588 | ATCTTTCTTCATTTG[C/T]ACAGTATACCAATAA | 81929 |
rs185495353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12968059 | AATATCAGTTCTTTT[A/C]GTGTGCCTTGGTCTT | 81929 |
rs185581198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12983410 | CCCAGACCTTCCTTT[C/T]CTCAGTGTAATTTGA | 81929 |
rs185725153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961017 | TCAAATGCATGGTTT[A/G]ATCTTGGACTTGGGT | 81929 |
rs186054793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12984936 | TGTATTTAAAATTTC[A/C]ACTATTTTTATATTG | 81929 |
rs186060747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12963044 | GATGTATCCAAGCTT[A/G]TATACCTAGTGAATG | 81929 |
rs186066573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12957483 | TTTATCGCTGTCTTT[A/G]CCTTATTGGATGTTT | 81929 |
rs186095971 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12981439 | GAGTGAATGCAACTC[C/T]GTCTGCCATCCCGGC | 81929 |
rs186203063 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12981798 | TTTTGAATTGTGAAT[C/T]TCAGTTCTTTTCTTT | 81929 |
rs186204846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957988 | TGCTGTGATTATAGG[C/T]GTGAGCCACTACGAG | 81929 |
rs186267160 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12980725 | CCCTCCCGGACGGGG[C/T]GGCTGGCCGGGCAGA | 81929 |
rs186282674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12974360 | CCTTGGCTCGCTTCA[A/G]CCTTTGCCTCCCGGG | 81929 |
rs186361938 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953415 | TTAGCTTTCTAAGAA[A/C]CTGCGAAACTCTTCC | 81929 |
rs186371887 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SEH1L | GRCh38.p7 | 18:12981113 | CTCAGACAGGGCGGC[C/T]GGGCAGAGATGCTCC | 81929 |
rs186448238 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12973457 | AGTGCGTGCCACCAC[A/G]CCTGGCTAATTTTTG | 81929 |
rs186458436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12953129 | GGAATTTTGAAATAC[A/G]TAGTCCTTTGTGTCT | 81929 |
rs186480253 | snp | G/T | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971162 | TTCTAGCTCTCGTGC[G/T]CATTCCCCCATGATC | 81929 |
rs186500525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949876 | TGAAACTCTGTACCC[A/G]AGAGCACCCTGTTCC | 81929 |
rs186572312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12957579 | ATTGAACTAGATTAT[A/G]TTTAAGACTCTTTCC | 81929 |
rs186941643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12954285 | GAAATTCTTTAAGAC[C/T]TTTGTATCCCTTCTC | 81929 |
rs187037073 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12967518 | GTGTAAAGGACATTC[A/G]TTTACCAATGACAGC | 81929 |
rs187082113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986085 | AGAGAAGCCATTAAA[A/T]TTTTACTAAAATTGT | 81929 |
rs187099922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12964295 | GCTGTCAATAGTTCT[A/G]TTTTCAGACTTTAAT | 81929 |
rs187125969 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12975632 | GCCAACAGGCCAGGC[A/C]GATTTTGGAGAGTGG | 81929 |
rs187193107 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985936 | GGACTAAGATGGAAA[C/T]ACTTTTTTTATAAGT | 81929 |
rs187246795 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959330 | GGATTTTGCAATATT[A/T]GCATTTATACTTACC | 81929 |
rs187252010 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946107 | TTCTGGAAAAGTCAA[A/T]ACCATGCAGTCAGTG | 81929 |
rs187253799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12968944 | TTAAGGCCAGGTGGG[G/T]TGGCTCACGTAATTC | 81929 |
rs187377456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986422 | TGTATTCCCAGTATC[A/C]TGTACGCACTAAAAA | 81929 |
rs187385134 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, splice-donor-variant | SEH1L | GRCh38.p7 | 18:12964496 | CTTCCACATCCCAAG[A/G]TATGACTAGATAGAT | 81929 |
rs187388446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12963703 | TATTGAAACCCATAC[A/T]TTTGATTGATTGATT | 81929 |
rs187724135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12958899 | TCATATGGTAGTTCT[A/G]TGTTTCACGTTTTTA | 81929 |
rs187806096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12960675 | AAAAGTTTTTTTGGC[A/G]TTAAGTCTGAGGTGT | 81929 |
rs187848974 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12954591 | CCCACCTCAGCCTCC[A/C]AAGCAGCTGGGACCG | 81929 |
rs187852720 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976355 | TGTTCCGTCCCCTGG[C/G]TAGAAAACAAGCCAC | 81929 |
rs187876764 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12982795 | TACTTTTAATGTCAT[A/T]TTAATTTATGTTATT | 81929 |
rs187899293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12976550 | GCTGCAGCATGTGTG[C/T]TCTTAGCTCCACCTG | 81929 |
rs187987386 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949071 | TCACCATGTGGGCCA[A/G]GCTGGTCTCGAACTC | 81929 |
rs188030514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12982230 | CTTGTGTGGGAGAAT[A/G]AAATCATCCTGTTTT | 81929 |
rs188094951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12953170 | CCTTTGCATGTTTTG[A/G]GGTTCATCCATATTG | 81929 |
rs188172416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12973551 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 81929 |
rs188188275 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SEH1L | GRCh38.p7 | 18:12955201 | CTAGATTTTTCTTTT[A/G]TTAGTAAAATGTCAG | 81929 |
rs188543474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12965341 | TATATTGCTTGTATA[A/C]TGGCAAGATTTATAA | 81929 |
rs188689897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961780 | CAAGCGATTCTCCTG[C/G]CTTAGCCTCTCTAGT | 81929 |
rs188690076 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12984563 | GGTCTTTGCATTAGG[A/T]CAAACTGAAATTTTA | 81929 |
rs188695766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12969666 | GCACTCCAGCCTGGC[A/G]ACAGAGTGAGACTCC | 81929 |
rs188849270 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987141 | GTTTTTCATTTTCTT[G/T]CAGAAGATTTTTCTA | 81929 |
rs188901731 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12956829 | CCACCATTTTACTTG[A/C]AAATTCTTTCTACAG | 81929 |
rs188989362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961140 | CCTGGGAGGGGCTGC[A/G]TGTGCAGTGTGTTTA | 81929 |
rs188991794 | snp | A/G | 0.0588605 | 0.161139 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949517 | GAGTGGGGTGGCGCA[A/G]TCTTGGCTCACTGCA | 81929 |
rs189123137 | snp | A/G | 0.039522 | 0.134904 | intron-variant | SEH1L | GRCh38.p7 | 18:12965170 | GGTGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 81929 |
rs189258574 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12983800 | CTAGTATCTGTAAGA[G/T]GGGTGGTGAAAGCTT | 81929 |
rs189524402 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12957085 | AAAAAAAAAAATTCT[A/G]TAAAAATTGTTTCTT | 81929 |
rs189596827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12979050 | GTTTTTTAAAAATGG[C/T]CTTTTACAGTTACTT | 81929 |
rs189652918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12950990 | CCATGCCTGGTTTCA[A/G]TATTTTTGCTTTACC | 81929 |
rs189782779 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965044 | TTTGAGGTGGAGTCT[C/T]GCTCTGTCACCCAGG | 81929 |
rs189794814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12966445 | GAGACACGTGTCACT[A/G]TGTCACCCAGGCTGG | 81929 |
rs189810142 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957484 | TTATCGCTGTCTTTG[C/T]CTTATTGGATGTTTG | 81929 |
rs189914484 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971373 | CTGATTTACTATAAT[A/G]TACCAAGTTCTGTGC | 81929 |
rs190080007 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SEH1L | GRCh38.p7 | 18:12977914 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGCTCAA | 81929 |
rs190201076 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947902 | GGCAGGGCTTGAGGG[A/G]CCAGGGGACTGTGTG | 81929 |
rs190208951 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12968135 | CTTATTTATATTTAT[C/G]AGTGAGTGACTGTTA | 81929 |
rs190352990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12964298 | GTCAATAGTTCTGTT[C/T]TCAGACTTTAATTCT | 81929 |
rs190375231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12972526 | CAGGTGATCAGATGG[A/G]CTTCGCAGGTACTAG | 81929 |
rs190392770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957753 | CCTCACCTGCCCTCC[C/T]TAATGGCATGATACT | 81929 |
rs190397220 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SEH1L | GRCh38.p7 | 18:12981731 | GGCAGTCTATTTAGG[A/G]AAAACTAAATTAGTA | 81929 |
rs190427630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986128 | ATTGTCAGCATTCCA[C/T]GTCTCAAGATTTTCT | 81929 |
rs190539471 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12954379 | TTTGCTCTTCCTACA[A/G]TAGTCTGTTATCGAT | 81929 |
rs190612488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12952183 | GATGTTTCATACATA[C/G]TTTTCTCTTAAAAAA | 81929 |
rs190663959 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12963913 | ACATGGGGTTTTACC[A/T]TGTTGGCCAGACTGG | 81929 |
rs190843818 | snp | A/T | 0.00378189 | 0.0433202 | intron-variant | SEH1L | GRCh38.p7 | 18:12963150 | TAAATTGTTATTATT[A/T]TTTTTTTAGGTTAAA | 81929 |
rs190860054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985696 | ATTTTAATTTGAAGA[C/T]TGAATAAATATTTTT | 81929 |
rs190896682 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985955 | TTTTTTATAAGTTTT[A/T]AATTCATAGTCACTA | 81929 |
rs191008062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12958170 | CTTACTGCATTCTCC[A/G]CCTCCGGGGTTCAAG | 81929 |
rs191153068 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SEH1L | GRCh38.p7 | 18:12976390 | CCCACTCACACTCAT[G/T]GGGAGGAGCCTCCAC | 81929 |
rs191153148 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12954977 | TACTCTGCTCCCAGC[C/T]GCTGGTAACCACTAA | 81929 |
rs191298215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12950384 | TTTAAAGGAGGAGCC[A/G]TGTATTTATTTGTAT | 81929 |
rs191319341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12953742 | ACTTCATTTACAGTG[C/T]TGTGTAACTACCACC | 81929 |
rs191448073 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12969029 | CAGTCTGACCAACAT[A/G]GAGAAAACCCTTCTC | 81929 |
rs191527614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12974489 | TTCACCATTTTGGCC[A/C]GGATGGTCTCCATCT | 81929 |
rs191606149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12975738 | TACCTTTTAGGGAGA[C/T]GACTTTGGCAGCTGT | 81929 |
rs191718283 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949075 | CATGTGGGCCAGGCT[C/G]GTCTCGAACTCCTGA | 81929 |
rs192012643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12960018 | TATGTGACTAGATCT[A/G]GTAAGGGAGGGGGAG | 81929 |
rs192084455 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947069 | CTCCTCCACTTTCCG[A/G]TTTTGGCAGAATCCT | 81929 |
rs192091365 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | SEH1L | GRCh38.p7 | 18:12982760 | CTCTGAAATATTTTT[A/T]GAAAATGGTCTTTTA | 81929 |
rs192161555 | snp | C/T | 0.134119 | 0.221521 | intron-variant | SEH1L | GRCh38.p7 | 18:12956999 | TGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 81929 |
rs192246658 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SEH1L | GRCh38.p7 | 18:12978449 | CCTCTCTGTCTCTGC[A/G]TTTCTTCTCTTCTTT | 81929 |
rs192262089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12965246 | CTCGATCTCCTGACC[G/T]TGTGATCCGCCCACC | 81929 |
rs192436499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12967967 | AGAATTGGGTTTTAT[A/G]GTTACAAATAAATTT | 81929 |
rs192641715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12983251 | TGTGATTTGTGCACC[A/G]CCATAGAATGGTGTC | 81929 |
rs192673514 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987336 | ACTTCAAAGTGCCTG[C/T]TCTGTAAATTTTATT | 81929 |
rs192691268 | snp | C/T | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949553 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 81929 |
rs192723314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12959011 | CTTCATCAGCACTTG[C/T]TGTGGTGCTATTTAT | 81929 |
rs192792324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12955786 | CATTTTAACTTGGGT[C/T]TGAAGCAATACTTAG | 81929 |
rs192875494 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972071 | GGATCTTCTATAGGT[A/G]TGACAAGTGTTTTGG | 81929 |
rs192903406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986777 | TTTGGTTCTCTTTGT[A/G]TTTACTACTTTTCTC | 81929 |
rs193007010 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976559 | TGTGTGCTCTTAGCT[C/T]CACCTGTCCTATTTC | 81929 |
rs193082856 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SEH1L | GRCh38.p7 | 18:12951236 | GTTTTTCATGATTTA[C/T]TTAGTGCAATGATTA | 81929 |
rs193149391 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SEH1L | GRCh38.p7 | 18:12960759 | TTTCTTTGAATTTCA[A/G]GATACTTATTTGTAT | 81929 |
rs193158140 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12964954 | TCCCCTCTCTTAAAA[A/T]AGAGGGAATTAGTTT | 81929 |
rs193302097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12969903 | TCAAAAAAACAGGAA[A/T]AAAACGCAAAAGGAA | 81929 |
rs199544910 | in-del | -/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986728 | TGAATATACTAAAGC[-/T]TTTTTTTTTTTTTCT | 81929 |
rs199636341 | snp | A/G | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946436 | TCTATTTTCTGCTCA[A/G]TTTTGCTGTGAACCT | 81929 |
rs199640502 | snp | C/T | 1.65384e-05 | 0.00287557 | intron-variant | SEH1L | GRCh38.p7 | 18:12955445 | CTGTTCTTTTCTTTT[C/T]TTTTTTTGATTCCCC | 81929 |
rs199700864 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986814 | TTGTGTTTTTTTTTT[C/T]CTGTTTTTGTTTTGT | 81929 |
rs199703025 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | SEH1L | GRCh38.p7 | 18:12957898 | TTATTTTGTAGAGAT[-/G]GGGTTTCACCATGTT | 81929 |
rs199727037 | in-del | -/C | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949112 | ATCCACCCGCCTCGG[-/C]CGCCTCGGCCTCCCA | 81929 |
rs199757952 | in-del | -/AAAGATT | 0.0283406 | 0.115616 | intron-variant | SEH1L | GRCh38.p7 | 18:12973190 | CCAGCAGTGTCAAAA[-/AAAGATT]AAAGATTTTTTTCTA | 81929 |
rs199759823 | in-del | -/T | 0.0297066 | 0.118198 | intron-variant | SEH1L | GRCh38.p7 | 18:12962388 | TAAGAAAAAAAAAAA[-/T]AATAATAATAATAGT | 81929 |
rs199763178 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | SEH1L | GRCh38.p7 | 18:12965280 | GCCTCCCAAACTGCT[-/G]GGATTACAGGCATGA | 81929 |
rs199811881 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971633 | GAGCGAAACCCTGCC[A/T]CAAAAAAAAAAAGAG | 81929 |
rs199814016 | snp | C/T | 4.94279e-05 | 0.00497107 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12963363 | TTGTATTTCTTGGAA[C/T]CCTTCAAGGTAAGTT | 81929 |
rs199816145 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970595 | GGCTAATTAAACAAA[-/T]TTTTTTTTTTGTAGA | 81929 |
rs199828651 | snp | C/G | 3.29506e-05 | 0.00405884 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12955533 | TTTTGGCTTCCTGTT[C/G]TTTTGACCGAACAGC | 81929 |
rs199838049 | in-del | -/T | 0.0418186 | 0.138422 | intron-variant | SEH1L | GRCh38.p7 | 18:12961675 | ACTTTATTGACTTAG[-/T]TTTTTTTTTGAGACA | 81929 |
rs199915355 | snp | A/C/G/T | 4.9436e-05 | 0.00497148 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978854 | TATTCTAGCAATAGC[A/C/G/T]ACCAAAGATGTGAGA | 81929 |
rs199990173 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953298 | TGTTGTTTTTGGCTG[G/T]TATGAGTAATGTTAA | 81929 |
rs200026117 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12982052 | TGTATTTTTAGTAGG[A/G]ATGGGGTTTCGCCAT | 81929 |
rs200082981 | in-del | -/TG | 0.0154538 | 0.0865337 | intron-variant | SEH1L | GRCh38.p7 | 18:12952089 | GAGAGTAAGAAAATC[-/TG]TAATTCTGTAGCATT | 81929 |
rs200102087 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12963252 | GTTAGCAACCTGTTC[C/T]GCAGATGGTATAGTA | 81929 |
rs200122984 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12984374 | GTCATAATATTTGCA[G/T]GTAGGTTATGAAGTC | 81929 |
rs200141163 | in-del | -/TC | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962457 | GAAATTGCATGCCTT[-/TC]TCTTTTTTTTTTTTT | 81929 |
rs200149743 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986803 | TTCTCTTTTTCTTGT[G/T]TTTTTTTTTTCCTGT | 81929 |
rs200167127 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974998 | TTTATTTTTATTTTA[-/T]TTTTTTTTTTTGAGA | 81929 |
rs200192978 | in-del | -/CCCCCCCCCC | 0.0456336 | 0.143994 | intron-variant | SEH1L | GRCh38.p7 | 18:12969212 | AAAACTCTGTACCCG[-/CCCCCCCCCC]CCCCCCCACCTCACC | 81929 |
rs200390009 | in-del | -/TT | 0.0283406 | 0.115616 | intron-variant | SEH1L | GRCh38.p7 | 18:12983781 | GCTCAGAGAATTGTC[-/TT]TGCTAGTATCTGTAA | 81929 |
rs200408195 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956900 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 81929 |
rs200687018 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971189 | GATCGCCGTAGGAAG[C/T]GATGACAGTAGCCCC | 81929 |
rs200750914 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957429 | TCAAAAAAAAAAAAA[-/A]TACACTCTCCTTTAT | 81929 |
rs200771866 | snp | G/T | 0.00159673 | 0.0282102 | intron-variant | SEH1L | GRCh38.p7 | 18:12955437 | ATGAGTATCTGTTCT[G/T]TTCTTTTTTTTTTTT | 81929 |
rs200809518 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12963186 | AACTCTGGTGGATAG[C/T]AGAACATCTGTTACT | 81929 |
rs200901292 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962459 | AAATTGCATGCCTTT[C/T]TTTTTTTTTTTTTTT | 81929 |
rs200987658 | in-del | -/T | 0.0437281 | 0.141251 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985938 | CTAAGATGGAAACAC[-/T]TTTTTTTATAAGTTT | 81929 |
rs201019425 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12982033 | CCTGGCTAATTTTTT[A/G]TTTTGTATTTTTAGT | 81929 |
rs201057542 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972107 | AACATGGTGGATTCA[C/T]GGCTAGGATGCTATG | 81929 |
rs201098722 | in-del | -/A | 0.31503 | 0.241394 | intron-variant | SEH1L | GRCh38.p7 | 18:12969687 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 81929 |
rs201118640 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971094 | TCCAGTGTGTTCATT[C/T]TGTGAATGAAATGTG | 81929 |
rs201174566 | snp | C/T | 0.0359639 | 0.129184 | intron-variant | SEH1L | GRCh38.p7 | 18:12955441 | GTATCTGTTCTTTTC[C/T]TTTTTTTTTTTGATT | 81929 |
rs201206357 | snp | G/T | 6.61332e-05 | 0.00574998 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12982531 | AGGAAAGAACTGACT[G/T]CCTCTGGTGGGCCAA | 81929 |
rs201281839 | in-del | -/GT | 0.0271762 | 0.113356 | intron-variant | SEH1L | GRCh38.p7 | 18:12954765 | GAGCCACTATGCCTG[-/GT]TGAATCAAATGAAAA | 81929 |
rs201293996 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967466 | CACTTTTAAAAAACA[A/C]AAAAATGTGAAAAAC | 81929 |
rs201352177 | snp | C/G | 1.6736e-05 | 0.0028927 | intron-variant | SEH1L | GRCh38.p7 | 18:12955649 | GGACCGGGAAGACAT[C/G]AGCAGCCAAGGAGCA | 81929 |
rs201370146 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971634 | AGCGAAACCCTGCCT[A/C]AAAAAAAAAAAGAGG | 81929 |
rs201451125 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12950117 | TGGCTTGTTGCAGCC[G/T]CAACATCCCAGGTTC | 81929 |
rs201532642 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974998 | TTTTATTTTTATTTT[A/T]TTTTTTTTTTTGAGA | 81929 |
rs201538151 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12985012 | GTACATGCATCAAAA[G/T]AATTTCAGGTTACCG | 81929 |
rs201596941 | in-del | -/G | 0.491987 | 0.0627894 | intron-variant | SEH1L | GRCh38.p7 | 18:12965106 | AGCTCCGCCTCCTGG[-/G]TTCAAGCGATTCCCC | 81929 |
rs201737177 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967050 | CACTATTTCCCTGTG[G/T]TTTCTAGTGAAGATT | 81929 |
rs201772773 | snp | A/G | 0.000317034 | 0.0125864 | intron-variant | SEH1L | GRCh38.p7 | 18:12955428 | CCTGGGATAATGAGT[A/G]TCTGTTCTTTTCTTT | 81929 |
rs201831408 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12982051 | TTGTATTTTTAGTAG[A/G]GATGGGGTTTCGCCA | 81929 |
rs201848221 | snp | C/G/T | 0.0588363 | 0.161119 | missense, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948135 | CCATGTTTGTGGCTC[C/G/T]CAGCATCGCGGCGGA | 81929 |
rs201854612 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971646 | CCTCAAAAAAAAAAA[A/G]AGGAGAAGGTAATTG | 81929 |
rs202002545 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | SEH1L | GRCh38.p7 | 18:12950096 | GGAGTGCAGTGGTGC[-/A]GATCTTGGCTTGTTG | 81929 |
rs202049745 | snp | C/G | 1.66391e-05 | 0.00288431 | intron-variant | SEH1L | GRCh38.p7 | 18:12955424 | AAGCCCTGGGATAAT[C/G]AGTATCTGTTCTTTT | 81929 |
rs202053257 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974999 | TTTATTTTTATTTTA[A/T]TTTTTTTTTTGAGAT | 81929 |
rs202065493 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979466 | GTCTCCCATGTCTAC[C/T]TCTTTCTACACAGAC | 81929 |
rs202112210 | snp | A/G | 0.00129465 | 0.0254096 | intron-variant | SEH1L | GRCh38.p7 | 18:12978736 | AAAATGTTAATGTCA[A/G]TTGTTTTTCCATTAG | 81929 |
rs202143910 | snp | A/G | 0.000559947 | 0.016723 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971206 | ATGACAGTAGCCCCA[A/G]CGCAATGGCCAAGGT | 81929 |
rs367563006 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964339 | AGTATATTTTTAAAG[A/G]ATTTACTTATACCTT | 81929 |
rs367747206 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12969670 | TCCAGCCTGGCGACA[A/G]AGTGAGACTCCATCT | 81929 |
rs367760887 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974921 | TTCTCTTTATTTACA[C/G]TCTCATTGAGGATCT | 81929 |
rs367878015 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12984891 | TCCTGTGGTTATATC[A/C]TCTTGTTATCCTATA | 81929 |
rs367967754 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12959419 | ACTCCTGGGTTCAAG[C/G/T]GATCCTCCACCTTGG | 81929 |
rs367997247 | in-del | -/C | 0.386504 | 0.209444 | intron-variant | SEH1L | GRCh38.p7 | 18:12980086 | CGGGCGGGGGGCTGA[-/C]CCCCCCCCACCTCCC | 81929 |
rs368119291 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | SEH1L | GRCh38.p7 | 18:12976708 | AGTGGCTCACGCCTG[-/T]AATCCCAGCACTTTG | 81929 |
rs368227577 | snp | A/C | 0.00230534 | 0.0338726 | intron-variant | SEH1L | GRCh38.p7 | 18:12951848 | TCTGCCTTTTATTTT[A/C]TTATAGGTCTGGGAT | 81929 |
rs368317100 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970633 | TCTTATTATGTGGCC[C/T]AGGTTCTTCTTGAAC | 81929 |
rs368328603 | snp | G/T | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948474 | TGCGCGCTCCCGCCC[G/T]CAGGGTACGCCGGGC | 81929 |
rs368330051 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12963236 | AGCACATGGGTCTTA[C/T]GTTAGCAACCTGTTC | 81929 |
rs368479205 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959426 | GGTTCAAGCGATCCT[C/G]CACCTTGGCCCCCCA | 81929 |
rs368494692 | in-del | -/TTTTTTCTTT | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974289 | TCTTTTTCTCTCTTT[-/TTTTTTCTTT]GAGATGGAGTCTCAC | 81929 |
rs368536335 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972421 | TAATTTTGGTCATGC[C/T]GAGATACAAGTGTCT | 81929 |
rs368586135 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12975955 | AGCAAAGAGGAGTGA[A/G]TGTGGTAAGCACAAT | 81929 |
rs368589849 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964705 | TGGTGGCATGATCTC[G/T]GCTCACTGCAAGCTC | 81929 |
rs368771027 | snp | A/G | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947880 | AGTCATGACGGGCCG[A/G]GGCGTGGGCAGGGCT | 81929 |
rs368812938 | snp | C/G | 0.000148629 | 0.0086193 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978888 | TTTACATTAAAGCCT[C/G]TGAGGTGAGTTTTAG | 81929 |
rs368813492 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12954608 | AGCAGCTGGGACCGT[A/G]AGTGCATACCACCAC | 81929 |
rs368830349 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962423 | CAAATGGGATTAACA[G/T]AAAATTATTCTTGAG | 81929 |
rs368838181 | snp | A/G | 0.273318 | 0.24891 | intron-variant | SEH1L | GRCh38.p7 | 18:12979643 | CTTCCCAGTAGGGGC[A/G]GCCGGGCAGAGGCGC | 81929 |
rs368863194 | snp | C/T | 0.000444543 | 0.0149021 | intron-variant | SEH1L | GRCh38.p7 | 18:12985225 | CTTTTCCATTTGTAT[C/T]ATGTCCTTTAACAGA | 81929 |
rs369038330 | multinucleotide-polymorphism | GTGTG/TTTTT | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949026 | GGCTAATCTTTTTTT[GTGTG/TTTTT]TGTATTTTTTAGTAG | 81929 |
rs369084553 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979563 | ATTGTCATCATGGCC[C/T]GTTCTCAATGAGCTG | 81929 |
rs369104899 | snp | A/G | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948753 | AACCATTTACATCCA[A/G]TGATTTCCCTGCTTG | 81929 |
rs369139415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12962267 | AGCTGGGCATGGTGG[C/T]AGGTGCCTGTCATCC | 81929 |
rs369195911 | snp | A/C/T | 0.000631725 | 0.0177632 | intron-variant | SEH1L | GRCh38.p7 | 18:12955413 | TAGGAAAAAAGAAGC[A/C/T]CTGGGATAATGAGTA | 81929 |
rs369214184 | snp | C/T | 4.4832e-05 | 0.00473434 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986853 | TTGTTCCTGTCTTCA[C/T]TGTTTCAGGTATTTC | 81929 |
rs369257177 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971651 | AAAAAAAAAAGAGGA[A/G]AAGGTAATTGATCTC | 81929 |
rs369372376 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987413 | GCTAATGTGAAAGCA[C/T]AATATTATGAAGTTT | 81929 |
rs369389355 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12963601 | TGTTTTCTATGCATA[G/T]GCAAATAACTATTTA | 81929 |
rs369406847 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967481 | CAAAAATGTGAAAAA[C/T]GTGAGGCGAACTGAC | 81929 |
rs369607063 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12973512 | ACCATGTTGGCCAGG[C/T]TTGTCTTGAACTCCT | 81929 |
rs369680959 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12978549 | AATTACATTTTCAAA[G/T]ACGCTATTTTTGAAT | 81929 |
rs369782838 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964590 | AATATATATATCTCT[A/C]CACATATTTATCAAT | 81929 |
rs369785032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12977574 | TACTAAAAATACAAA[A/G]TTAGCCAGGCGTAGT | 81929 |
rs369825089 | snp | A/C | 0.000181862 | 0.00953403 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987011 | ACCCTCGCAGACGAT[A/C]TCTCTCTCGGCCTCT | 81929 |
rs369905379 | in-del | GTGTG/TTTT | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949027 | GCTAATCTTTTTTTT[GTGTG/TTTT]TGTATTTTTTAGTAG | 81929 |
rs370049753 | snp | G/T | 1.65586e-05 | 0.00287733 | intron-variant | SEH1L | GRCh38.p7 | 18:12951847 | ATCTGCCTTTTATTT[G/T]CTTATAGGTCTGGGA | 81929 |
rs370062596 | in-del | -/TC | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964630 | ATATATTTACTCCCG[-/TC]TCTTTTTTTTTTTTT | 81929 |
rs370117073 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12980854 | CTTCCGGACGGGGCG[A/G]CTGGCCGGGCGGGGG | 81929 |
rs370172265 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964425 | ATGTTCTTGCTATGT[A/T]ATCATTAAAGAATAT | 81929 |
rs370362403 | snp | C/T | 0.294832 | 0.245947 | intron-variant | SEH1L | GRCh38.p7 | 18:12980605 | GACGGGGCAGCTGGC[C/T]GGGCAGAGGGGCTCC | 81929 |
rs370370485 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974571 | GTGTGAGCCACCACG[C/T]CCGGCCTGTTTATCT | 81929 |
rs370373158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12963861 | AGAATTACAGGCATG[C/T]GCCACCACGTCTGCC | 81929 |
rs370377593 | snp | C/G | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947670 | GCCGCCGAACGGTCA[C/G]AGCCTGGAGGAACCC | 81929 |
rs370442446 | snp | C/T | 3.85996e-05 | 0.00439298 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948262 | TGCGGGCGGGGCCGA[C/T]CCCGGAAGGAAGGAA | 81929 |
rs370505862 | snp | G/T | 3.73902e-05 | 0.00432362 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948145 | GGCTCGCAGCATCGC[G/T]GCGGACCACAAGGAT | 81929 |
rs370614756 | in-del | GG/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977031 | GGAGGGGGCTGAGAT[GG/T]CTGGATTTCCCAGAA | 81929 |
rs370630400 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12950082 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGCG | 81929 |
rs370671688 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12955529 | CAGGTTTTGGCTTCC[C/T]GTTCTTTTGACCGAA | 81929 |
rs370692887 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958515 | CATATTTTTAAAGAA[G/T]GCCTCCCCCTTCCTC | 81929 |
rs370698687 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | SEH1L | GRCh38.p7 | 18:12984035 | TTTGATTATTTTCCT[G/T]TCAGCTAATTATATG | 81929 |
rs370700080 | snp | C/T | 1.66032e-05 | 0.0028812 | intron-variant | SEH1L | GRCh38.p7 | 18:12982688 | AAGGTAAGAGTTCAG[C/T]GAAGGGGTAATTGTT | 81929 |
rs370714258 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958284 | AGAGACAGGGTTTCA[C/T]CATGTTGGTCAGGCT | 81929 |
rs370738853 | in-del | -/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959418 | AACTCCTGGGTTCAA[-/G]CGATCCTCCACCTTG | 81929 |
rs370806736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12953713 | ATTTCAGAGTAAACA[A/G]TTAATTGGCATTTAC | 81929 |
rs370888540 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971315 | TTTAAAATGTTATTT[C/G]TTTATTCATTTACAG | 81929 |
rs370997240 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974535 | CGCCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT | 81929 |
rs371012262 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977496 | TTGGGAGGCAGAGGC[A/G]GGTGGATCACCTGAG | 81929 |
rs371020100 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12983101 | CCATAAGTTAAGAGC[C/T]TTGGGGGCCCTGATT | 81929 |
rs371171674 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SEH1L | GRCh38.p7 | 18:12980027 | ACCTCCCTCCCGGAC[A/G]GGCGGCTGACCCCCC | 81929 |
rs371191121 | snp | A/G | 0.000659098 | 0.0181415 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971243 | TTTTGAATATAATGA[A/G]AACACCAGGTCAGTC | 81929 |
rs371240694 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12975115 | CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT | 81929 |
rs371459372 | snp | A/G | 8.23906e-05 | 0.00641783 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984100 | ATGGGAGCCCAGTCA[A/G]TGGGAGTTCTCAGCA | 81929 |
rs371642314 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978371 | GCTCCTGCTGGCTCC[A/C/G]GGAGTTCTTTGGCTT | 81929 |
rs371736675 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959773 | TTGGTGTTATATCCA[A/G]GAAAGCATTGCCAAA | 81929 |
rs371849114 | snp | A/C | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948674 | TTCTCTCACCAGGGC[A/C]CATGGTTTTCTCCGT | 81929 |
rs371893373 | snp | A/G | 6.61923e-05 | 0.00575254 | intron-variant | SEH1L | GRCh38.p7 | 18:12963407 | TCTGATAACATCCTA[A/G]TAAAATAAACTAGTA | 81929 |
rs371910475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12981189 | CCTAGATGGGATGGC[A/G]GCCGGGCAGAGACGC | 81929 |
rs372017827 | snp | C/G | 0.000107145 | 0.00731853 | missense, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986891 | CTCTGGATTCCCCAC[C/G]GGCTGGATCGAGATG | 81929 |
rs372268351 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977023 | AGGCCCCAGGAGGGG[C/G]CTGAGATTCTGGATT | 81929 |
rs372380906 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970138 | AGCTTTAAGAGGTTA[C/G]TAGTGCACAATACTG | 81929 |
rs372431736 | snp | G/T | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947182 | GCAGCCCACTTCCCC[G/T]GCCGCTTCCTTCCCC | 81929 |
rs372472266 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985342 | TTCCCCTTCCCCAGC[A/G]CCGTTTGACCTCTCC | 81929 |
rs372479691 | in-del | -/GT | | | intron-variant | SEH1L | GRCh38.p7 | 18:12952090 | AGAGTAAGAAAATCT[-/GT]AATTCTGTAGCATTC | 81929 |
rs372573953 | snp | C/T | 1.77656e-05 | 0.00298035 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948166 | CCACAAGGATCTCAT[C/T]CACGATGTCTCTTTC | 81929 |
rs372682457 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986106 | CTAAAATTGTGCATG[C/T]AAATTAATTGTCAGC | 81929 |
rs372715497 | snp | C/T | 1.65277e-05 | 0.00287464 | missense, utr-variant-5-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12951885 | GAAAGTGGTGATTGG[C/T]ATTGTACTGCTAGCT | 81929 |
rs372748245 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12977584 | ACAAAATTAGCCAGG[C/T]GTAGTGGTGCACGCT | 81929 |
rs372822658 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971648 | TCAAAAAAAAAAAGA[A/G]GAGAAGGTAATTGAT | 81929 |
rs372881524 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12987439 | AGTTTATTCTGCCTT[A/G]TGAGACCTTAAAAAA | 81929 |
rs372921378 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956146 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTACCTC | 81929 |
rs372997937 | in-del | -/TATATA | | | intron-variant | SEH1L | GRCh38.p7 | 18:12982457 | ATATATATGTGTGTG[-/TATATA]TATATATATATGTTT | 81929 |
rs373004325 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12981444 | AATGCAACTCCGTCT[C/G]CCATCCCGGCACCTC | 81929 |
rs373015480 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12983060 | GGAGAAAATCCAGTA[C/T]CTTCCCTGCTTCTTC | 81929 |
rs373058451 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972065 | TCAGATGGATCTTCT[A/G]TAGGTGTGACAAGTG | 81929 |
rs373059011 | snp | C/T | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949165 | AGCCACCGCGCCCGG[C/T]CTACAAGCAGAATTT | 81929 |
rs373104350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12963647 | CATATATGCAAACAC[A/G]CCCAGATATTCACTA | 81929 |
rs373227234 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | SEH1L | GRCh38.p7 | 18:12978908 | GTGAGTTTTAGAAGC[A/G]TTTATGAATTTGAAA | 81929 |
rs373238512 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957585 | CTAGATTATATTTAA[G/T]ACTCTTTCCAGCATT | 81929 |
rs373272137 | snp | C/G | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948884 | AGACCGAGTCTCACT[C/G]TGTCACCCAGGCTGG | 81929 |
rs373308482 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12954863 | TTAGTGATTTTAAGT[A/G]TATTCATTTAATTGG | 81929 |
rs373411410 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974103 | AAGAGTGTCTGCAGG[C/T]GGGGGTGTGTGCTAT | 81929 |
rs373480284 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12982075 | TTCGCCATGTTGGCC[A/G]GGCTGGTCTTGAACT | 81929 |
rs373588669 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12980329 | GCGGCCGGGCAGAGG[C/T]GCCCCTCACCTCCCG | 81929 |
rs373647238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12969538 | ACTAAAGATACAAAA[A/G]TTAGCTGGGCGTGGT | 81929 |
rs373697637 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959660 | TCTCCCGTTCTGTGG[A/G]TTGCCTTTTTCACTC | 81929 |
rs373702875 | snp | A/G | 4.94344e-05 | 0.00497139 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984120 | AGTTCTCAGCAGGGA[A/G]CCTCAAATCCTTCCC | 81929 |
rs373766082 | snp | C/T | 0.268724 | 0.249298 | intron-variant | SEH1L | GRCh38.p7 | 18:12980889 | ACCCCCCCCACCTCC[C/T]TTCCGGACGGGGCGG | 81929 |
rs373829303 | snp | A/G | 0.0667028 | 0.170006 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947832 | GACGGGCCTGGGGGC[A/G]GGGCGGGGCTTGAGG | 81929 |
rs373870345 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SEH1L | GRCh38.p7 | 18:12974294 | TTCTCTCTTTTTTTT[C/T]CTTTGAGATGGAGTC | 81929 |
rs373878313 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979595 | TGAGTACACCTCCCA[C/G]ACGGGGTGGTGGCTG | 81929 |
rs373973930 | snp | C/G | 0.000802045 | 0.0200095 | intron-variant | SEH1L | GRCh38.p7 | 18:12955639 | AGTATTCTGGGGACC[C/G]GGAAGACATGAGCAG | 81929 |
rs373980702 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12978807 | CCTGTTCATGATATT[G/T]CATTCGCTCCAAATT | 81929 |
rs373993947 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12984679 | GGAAATAATAAAACA[C/T]GAGATTGATTTTTAG | 81929 |
rs373996355 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SEH1L | GRCh38.p7 | 18:12968700 | ATTTCTAGCCCTGTA[C/T]GATAATATTCTTTCA | 81929 |
rs374023345 | snp | A/G | 0.129664 | 0.219133 | intron-variant | SEH1L | GRCh38.p7 | 18:12980606 | ACGGGGCAGCTGGCC[A/G]GGCAGAGGGGCTCCT | 81929 |
rs374357044 | snp | C/T | 1.68363e-05 | 0.00290136 | intron-variant | SEH1L | GRCh38.p7 | 18:12982721 | TTTATATTTCTGCTC[C/T]GCAATTTTTACTTAA | 81929 |
rs374511502 | snp | C/G | | | intron-variant, missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12964465 | TAGAAAAGATGAATA[C/G]AGCACATTTATACAA | 81929 |
rs374556599 | snp | A/G/T | 9.88826e-05 | 0.00703076 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12984082 | CTGGTATTTTGAAAG[A/G/T]TAATGGGAGCCCAGT | 81929 |
rs374604797 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958730 | GTGTGTATACCACAT[G/T]TTGTTTATCCATTCA | 81929 |
rs374676889 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977615 | TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAAGCA | 81929 |
rs374718956 | snp | A/G | 6.58935e-05 | 0.00573955 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971181 | TCCCCCATGATCGCC[A/G]TAGGAAGTGATGACA | 81929 |
rs374860079 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967023 | TTATACCAGTTTTTG[G/T]TACATGTATTACACT | 81929 |
rs374938350 | in-del | -/GTAGTTGTATTTCT | | | frameshift-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12963344 | CATGTAAGCTAAGCT[-/GTAGTTGTATTTCT]TGGAACCCTTCAAGG | 81929 |
rs374989571 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956422 | TGGGCCCATGTCACA[C/T]GCCATACAGATCCAC | 81929 |
rs375144252 | snp | A/G | 6.58924e-05 | 0.0057395 | missense, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12971188 | TGATCGCCGTAGGAA[A/G]TGATGACAGTAGCCC | 81929 |
rs375179934 | snp | C/T | 4.95356e-05 | 0.00497648 | stop-gained, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986986 | GACACTGCCAACCTC[C/T]AGTATCCTCACCCTC | 81929 |
rs375209158 | in-del | -/TACT | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986643 | CCTTTCAAGTTTCTA[-/TACT]TGCTTAAGCAATCTT | 81929 |
rs375374915 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12959390 | CTTAATAGAGTTGCC[C/T]AGGCTGGTCTTGAAC | 81929 |
rs375393182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12954886 | TTAATTGGCAACCAC[C/T]ACCACTTCTAATTTC | 81929 |
rs375399597 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12963448 | TAACAATTTGATAAT[G/T]TATTCTCTCAAAGGT | 81929 |
rs375532816 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12975522 | AAGACAGAGGGTGTT[A/C]TGCAAGCAGAGAGGA | 81929 |
rs375538896 | snp | C/G | | | intron-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12975853 | GAGGGACCGGGGAGA[C/G]TTGTCTAGGAGGCAC | 81929 |
rs375645784 | snp | G/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12985483 | AAATATAAACGGAGA[G/T]GCTTTCTGTTGAGAC | 81929 |
rs375654782 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979525 | TCCCCACCTTTCCCC[C/G]CTTTCTATTCCACAA | 81929 |
rs375759750 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12971649 | CAAAAAAAAAAAGAG[A/G]AGAAGGTAATTGATC | 81929 |
rs375826810 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12951332 | TGTCTCTGTTACCTA[A/G]TAGAGCTCAGCTTCC | 81929 |
rs375889149 | in-del | -/TTCTT | | | intron-variant | SEH1L | GRCh38.p7 | 18:12951846 | TATCTGCCTTTTATT[-/TTCTT]ATAGGTCTGGGATAA | 81929 |
rs375978463 | in-del | GTG/TT | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12949029 | TAATCTTTTTTTTTT[GTG/TT]TGTATTTTTTAGTAG | 81929 |
rs376254002 | in-del | -/TT | | | downstream-variant-500B, utr-variant-3-prime | SEH1L | GRCh38.p7 | 18:12987553 | GTGGACTTTTTGGTC[-/TT]TTTTTTTTTTTTTTT | 81929 |
rs376260185 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12963827 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 81929 |
rs376381695 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979609 | AGACGGGGTGGTGGC[C/T]GGGCAGAGGGGCTCC | 81929 |
rs376406726 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12964065 | TTTCACTTAAAGATA[C/G]ATTGTGGGCATTTTT | 81929 |
rs376463153 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957145 | GAAATATACTGTCCT[C/T]GGCCGGGTGCGGTGG | 81929 |
rs376523131 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12966070 | CTTATCACTTACCAT[C/T]TGTTTTTTATTTTTA | 81929 |
rs376554962 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977034 | GGGGCTGAGATTCTG[-/A]GATTTCCCAGAAGCT | 81929 |
rs376562047 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962200 | CAGGAGTTTGAGACC[C/T]ATCTGGGCAACATAG | 81929 |
rs376705003 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977450 | TCAATTCCTGCTGGG[C/T]GCAGTGGCTCACACC | 81929 |
rs376747252 | snp | A/G | 1.65023e-05 | 0.00287244 | intron-variant | SEH1L | GRCh38.p7 | 18:12971132 | TTTGTTATCTAAAAT[A/G]TTCTTTCTCCCCGTT | 81929 |
rs376751843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12979278 | GATGACTCTTAACGA[A/G]CATGCTGCCTTCAAG | 81929 |
rs376771409 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12980573 | GGCGGGGGGCTGACC[C/T]CCCCACCTCCCTCCC | 81929 |
rs376782608 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12981850 | CTTGCTGCCCTGCCC[-/A]TTTTTTTTTTTTTTT | 81929 |
rs376823500 | snp | A/C | 0.264358 | 0.249587 | intron-variant | SEH1L | GRCh38.p7 | 18:12981234 | ACTGGGCAGCCAGGC[A/C]GAGAGGCTCCTCACA | 81929 |
rs376853740 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956312 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 81929 |
rs376872225 | snp | A/T | 5.014e-05 | 0.00500674 | intron-variant | SEH1L | GRCh38.p7 | 18:12955648 | GGGACCGGGAAGACA[A/T]GAGCAGCCAAGGAGC | 81929 |
rs376953677 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962679 | TGTCTTGCCATGTAG[C/T]CCAGGCTGGTCTTGA | 81929 |
rs376996010 | snp | A/C | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948392 | GAAGCCCTCCCCGCC[A/C]GCGTATTGTGGGGTC | 81929 |
rs377060813 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965009 | TTCCATTTCCTCATT[C/T]TTTTTTTTTTTTTTT | 81929 |
rs377188581 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957591 | TATATTTAAGACTCT[C/T]TCCAGCATTTTCATA | 81929 |
rs377194560 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976379 | AAGCCACGGGCCCCA[C/T]TCACACTCATGGGGA | 81929 |
rs377246665 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948184 | CGATGTCTCTTTCGA[C/T]TTCCACGGGCGGCGG | 81929 |
rs377373014 | snp | A/G | 0.0019421 | 0.0311011 | intron-variant | SEH1L | GRCh38.p7 | 18:12984011 | ATTGGTATTAATCAT[A/G]TTAATGTATTTGATT | 81929 |
rs377451628 | snp | A/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958213 | CTCAGTCTCCTGAGT[A/T]GCTGGGACTACAGGC | 81929 |
rs377456262 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949610 | GGCGCCCGCCACCAC[A/G]CCCGGCTAATTTTTT | 81929 |
rs377480400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12974405 | CTGCCTCAGCCTCCC[C/T]GGTAGCTGGGACTAC | 81929 |
rs377489068 | snp | C/T | 0.319616 | 0.240112 | intron-variant | SEH1L | GRCh38.p7 | 18:12979996 | GCGGCTGGCCGGGCG[C/T]GGGGCTGACCCCCCC | 81929 |
rs377602105 | snp | A/G/T | 0.000214143 | 0.0103454 | synonymous-codon, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12982608 | TCAGGTCTGGCGAGT[A/G/T]AGTTGGAATATAACA | 81929 |
rs377602381 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12949966 | GTACCTCAGATAAAT[A/G]GAATCATAGAATATT | 81929 |
rs377723866 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12956423 | GGGCCCATGTCACAC[G/T]CCATACAGATCCACT | 81929 |
rs386801388 | in-del | ACG/CA | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972905 | GACATAAGCCCAAAA[ACG/CA]TAAAAGGTGTATCAT | 81929 |
rs397719900 | in-del | -/T | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12963157 | TTATTATTTTTTTTT[-/T]AGGTTAAAAGGACAA | 81929 |
rs397822158 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12967053 | ATTTCCCTGTGGTTT[-/T]CTAGTGAAGATTTTT | 81929 |
rs397841634 | in-del | -/T | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946944 | CTCATTTTTTTTTTT[-/T]CTGTACTTTCGCTCC | 81929 |
rs397858199 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12966109 | GTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTTG | 81929 |
rs397858470 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12973321 | ATTTTTTTTTTTTTT[-/T]GAGAGTCTCACTCTG | 81929 |
rs397858857 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12972905 | GACATAAGCCCAAAA[-/A]CGTAAAAGGTGTATC | 81929 |
rs397933439 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12979087 | TTTCTTTTTTTTTTT[-/T]ATTGATCATTCTTGG | 81929 |
rs397975377 | in-del | -/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974997 | TTTTATTTTTATTTT[-/T]ATTTTTTTTTTTGAG | 81929 |
rs398032025 | in-del | -/A | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12952204 | TCTTAAAAAAAAAAA[-/A]CAAAACCTTTACTCA | 81929 |
rs398032026 | in-del | -/A | 0 | 0 | intron-variant | SEH1L | GRCh38.p7 | 18:12956467 | ATCAAAAAAAAAAAA[-/A]GAAAAGAACAGATAC | 81929 |
rs398079278 | in-del | -/T | | | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12946943 | CCTCATTTTTTTTTT[-/T]TCTGTACTTTCGCTC | 81929 |
rs398079279 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12962226 | CATAGTGAGACCCCC[-/C]CATCTCTATAAAAAT | 81929 |
rs398120193 | in-del | -/A | | | intron-variant | SEH1L | GRCh38.p7 | 18:12957080 | CAAAAAAAAAAAAAA[-/A]TTCTATAAAAATTGT | 81929 |
rs527278514 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12976983 | TCTGTCTCAAAAAAA[A/T]AAAAAAAGCATATTC | 81929 |
rs527312199 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12983220 | CTTGGATGATTATCC[A/G]TTAGGCAGAGATGTC | 81929 |
rs527345062 | snp | A/G | 3.9208e-05 | 0.00442747 | intron-variant | SEH1L | GRCh38.p7 | 18:12982467 | TGTGTGTATATATAT[A/G]TGTTTTAAAACTTTG | 81929 |
rs527400741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949698 | GACCTCGTGATCCGC[C/T]CACCTCGGCCTCCCA | 81929 |
rs527454857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12977007 | CATATTCTGATTGTG[C/T]AGGCCCCAGGAGGGG | 81929 |
rs527456542 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12949984 | ATCATAGAATATTCG[C/T]CCTTTTATATTTGGT | 81929 |
rs527502021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12963000 | TATGTGGTATTTTGC[C/T]ATGTACTTGTAGGAA | 81929 |
rs527643036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12951196 | ACCAGGCGATACTCT[A/G]TTTTGGCTCATACTG | 81929 |
rs527817702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12956410 | CCAAATTCAGGATGG[A/G]CCCATGTCACACGCC | 81929 |
rs527948302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12985049 | ATACCAGATTATAAA[C/G]ATTATTTCATGAAAC | 81929 |
rs527984265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12974924 | TCTTTATTTACACTC[G/T]CATTGAGGATCTTAT | 81929 |
rs528051942 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12968750 | GAGGGAGGCGGAGAT[A/C]CAGGTGATCTGTCTA | 81929 |
rs528185039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12960083 | TTGGTCTCAGGTAAC[A/G]CCTTGAGCAACCAGA | 81929 |
rs528276049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12975243 | GTGATCTGCCTGCTT[C/T]GGCCTCCCAAAGTGT | 81929 |
rs528317347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12981184 | CACTTCCTAGATGGG[A/G]TGGCGGCCGGGCAGA | 81929 |
rs528460284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12969785 | TAATCCCAGCTACTC[A/G]GGAGACTGAGACAGG | 81929 |
rs528487811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12969464 | GGAGGCCGAGGTGGG[C/T]GGATCATGAGGTCAG | 81929 |
rs528565113 | in-del | -/A | 0.00424406 | 0.0458696 | intron-variant | SEH1L | GRCh38.p7 | 18:12963147 | ATTTAAATTGTTATT[-/A]TTTTTTTTTTAGGTT | 81929 |
rs528625322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12975781 | CAGGAACTCAGGGAT[C/G]AATGCAGTAGCCCAC | 81929 |
rs528660069 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12960732 | TTTGGGAGTGGTGGC[A/G]TAAGAAGGACTTTTC | 81929 |
rs528792920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961872 | GGGTTTCACCATGTT[A/G]GACAGGCTGGTCTTG | 81929 |
rs528855225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948518 | GCGCTGCCGGGGCTG[C/T]GGGCGGGAACCCAGG | 81929 |
rs528958165 | snp | G/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976835 | AAAAACATTGGCCGG[G/T]CGTGGTGGCAGGCCC | 81929 |
rs528995697 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12948040 | GCTCCCGGGCTGCGA[A/G]GTCTGGCTAGGCTAC | 81929 |
rs528997725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12954293 | TTAAGACCTTTGTAT[C/T]CCTTCTCCAGCCACC | 81929 |
rs529083215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12976504 | GAGAACTTGCTGAAG[A/G]TCGTTACAGCCTGGA | 81929 |
rs529105191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12975918 | TAGCTGATGGTAGTG[C/T]CACTTGTTGAGATGG | 81929 |
rs529105812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12982441 | GAATTTTACGTGTGT[A/G]TATATATATGTGTGT | 81929 |
rs529216860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12981682 | AACAATTCTCCAAAT[A/C]TAACTGATAATCTAT | 81929 |
rs529280518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12961997 | TAAAGTTTCATCTTA[C/T]CTGTGTGCCAGAAGA | 81929 |
rs529312912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12970483 | TAGAGTGCAGTGGCA[C/T]GATCATAGCTCACTG | 81929 |
rs529359645 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12977841 | CCTTTTTTATTTTTT[A/G]TTTTTGCAGTTGAGT | 81929 |
rs529442261 | in-del | -/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12964633 | TATTTACTCCCGTCT[-/C]TTTTTTTTTTTTTTT | 81929 |
rs529445385 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12983373 | GCCTCCCATGTTCAA[A/T]TTTGGGCTTTGGTAA | 81929 |
rs529455314 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SEH1L | GRCh38.p7 | 18:12969858 | GATCGCCACTGCACT[C/G]CAGCCTGGGTGACAG | 81929 |
rs529615388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957746 | TATTACCCCTCACCT[C/G]CCCTCCCTAATGGCA | 81929 |
rs529704687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12965893 | TTCATTAGAGAAAAT[G/T]TCAGATACACCAGAA | 81929 |
rs529726036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12973546 | CTCAGGTGATCCACC[C/T]ACCTCGGCCTCCCAA | 81929 |
rs529768058 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12958944 | TTTCCATAGCAGCTA[C/T]ACCATTTTACATTCC | 81929 |
rs529786383 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12974389 | GGTTCAAGCGATTCT[C/G]CTGCCTCAGCCTCCC | 81929 |
rs529841404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12972886 | TGAGCAGAATGAATA[C/T]GTAGACATAAGCCCA | 81929 |
rs529874164 | in-del | -/T | 0.0135831 | 0.0812837 | intron-variant | SEH1L | GRCh38.p7 | 18:12954642 | GACTAATTTTTTGTA[-/T]TTTTTTGTAGTGATG | 81929 |
rs529976823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12958258 | CTGGCTAATTTTTTT[G/T]TGTTTTTAGAAGAGA | 81929 |
rs530055321 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12980798 | CCCTCACCTCCCGGA[C/T]GGGGCGGCTGGCCGG | 81929 |
rs530093120 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12979987 | CCGGACGGGGCGGCT[C/G]GCCGGGCGCGGGGCT | 81929 |
rs530238301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12968371 | GATGAACCATTGGGG[C/T]GCAGTTCCTTCCTCC | 81929 |
rs530371217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12975043 | TGTTGCCCAGGTTGG[A/G]GTGCAATGGTGTGAT | 81929 |
rs530379084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12959149 | TCAATTGTATGTCTT[C/T]CTGGGGAAAATACTA | 81929 |
rs530470164 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12967787 | GGCGTGGTGGTGTGC[A/G]CCTGTACTCCCAGCT | 81929 |
rs530478199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12952341 | GGGTTCAAGTGATTC[C/T]TCTGCCTCAGCCTCC | 81929 |
rs530617194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12958376 | CAGGCGTGAGCCACC[A/G]TGCCTGGCCCATTTT | 81929 |
rs530656607 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947705 | CAGGATCGTAGGGCA[G/T]GACGGGCCGGGGGCG | 81929 |
rs530657258 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12971921 | AGAGGGAGTATATTT[-/A]ATACTGTTGTTGGAA | 81929 |
rs530665763 | in-del | -/AG | 0.00159617 | 0.0282053 | downstream-variant-500B | SEH1L | GRCh38.p7 | 18:12987693 | TTGCCTTATAAAAAC[-/AG]AATGTATTTTATTTA | 81929 |
rs530689157 | snp | G/T | | | intron-variant, upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12948682 | CCAGGGCACATGGTT[G/T]TCTCCGTGGGTTCAG | 81929 |
rs530692378 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947334 | CTTCTGATCCTTTCC[A/T]CCCCGTCCAGCCTTC | 81929 |
rs530710026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12980848 | ACTTCCCTTCCGGAC[A/G]GGGCGGCTGGCCGGG | 81929 |
rs530724646 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12983778 | GTAGCTCAGAGAATT[A/G]TCTTTGCTAGTATCT | 81929 |
rs530726795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12952943 | CATGCCACCACACCC[A/G]GCTAATTTTTGTAGT | 81929 |
rs530851023 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | SEH1L | GRCh38.p7 | 18:12954194 | TAGCTATACAGTGTG[-/A]AACACATTTTCTGAA | 81929 |
rs530867950 | snp | C/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12983068 | TCCAGTATCTTCCCT[C/G]CTTCTTCTCTGCAGC | 81929 |
rs530946920 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SEH1L | GRCh38.p7 | 18:12981152 | CAGATGATGGGCGGC[C/T]GGGCAGAGACGCTCC | 81929 |
rs531098385 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12961089 | CTGATTCTTCCCTTG[G/T]GGTGGGCAGTCCGCA | 81929 |
rs531139965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12969280 | AAATCTCACATTTTT[A/T]TAGCTGGGTGTGGTG | 81929 |
rs531163858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12981660 | GTGCTTTATTTAGGC[C/T]GAAACTAACAATTCT | 81929 |
rs531174807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978262 | TCAGGTGGCTTAACA[C/G]AGAAATGTATTCACT | 81929 |
rs531175663 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | SEH1L | GRCh38.p7 | 18:12971255 | TGAAAACACCAGGTC[A/G]GTCCTGCTTTGGTTT | 81929 |
rs531454167 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12970331 | AATGAGGTTGACCAC[A/C]GATGAGTCTAGGGAG | 81929 |
rs531485565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957165 | GGGTGCGGTGGCTCA[C/T]GCCTATAATCCCAGC | 81929 |
rs531626682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12977390 | AGAAATAGAATTGCA[A/G]GGATGAAATAGCCTT | 81929 |
rs531643787 | snp | C/T | | | intron-variant | SEH1L | GRCh38.p7 | 18:12953008 | GCTGGTCTCGAACTC[C/T]TGACCTCAAGTGATC | 81929 |
rs531748494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12957577 | ACATTGAACTAGATT[A/G]TATTTAAGACTCTTT | 81929 |
rs531891162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SEH1L | GRCh38.p7 | 18:12949690 | TATCTCCTGACCTCG[G/T]GATCCGCCCACCTCG | 81929 |
rs531948327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12972931 | GTATCATTGGCCACG[C/T]GAGGTGACTTATGCC | 81929 |
rs531951057 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SEH1L | GRCh38.p7 | 18:12947092 | AGAATCCTTGATCTG[A/T]GCCAGGCCTCTTCCC | 81929 |
rs531953368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | SEH1L | GRCh38.p7 | 18:12986626 | GTTTAACAGATTGTA[A/T]TCCTTTCAAGTTTCT | 81929 |
rs531976180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12972839 | AGGCTTCATGAAGTG[C/T]TGGGCTTGTTAAAGT | 81929 |
rs532013173 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965259 | CCTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 81929 |
rs532055411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12960349 | AGGGTGCTGAAATCT[A/G]GTTTTCCCAGCACCA | 81929 |
rs532074519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12978983 | GAGGTAACTATGATT[G/T]GGTTTATATTTCTGC | 81929 |
rs532136446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12972105 | GAAACATGGTGGATT[C/T]ACGGCTAGGATGCTA | 81929 |
rs532265659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12957636 | TCTGCATGCTTTTTT[C/T]CCCCCTTTATGATTT | 81929 |
rs532272626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SEH1L | GRCh38.p7 | 18:12978294 | ACAGTTCTGGAGGTC[A/G]GAAGTCTGAAATCAA | 81929 |
rs532301963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12957301 | AGCATGGTGGCACAT[C/G]CCTGTAATCCCAGCT | 81929 |
rs532303323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12965766 | TTTATGATGGATTTT[A/G]ATAGCCAATGGAAAT | 81929 |
rs532357706 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12979846 | GCACCCCTCACCTCC[C/T]GAATGGGGCGGCTGG | 81929 |
rs532514607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12952239 | GAAATTTTCTTTTTT[C/T]TTTTTTTTTGAGACG | 81929 |
rs532630082 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SEH1L | GRCh38.p7 | 18:12954116 | TACCTTTAGTTGGTG[-/A]CATTGTTACCATGTA | 81929 |
rs532716261 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | SEH1L | GRCh38.p7 | 18:12980616 | TGGCCGGGCAGAGGG[A/G]CTCCTCTCTTCCCAG | 81929 |
rs532723112 | snp | A/C | | | intron-variant | SEH1L | GRCh38.p7 | 18:12965534 | ACCTGAAAATGTCTT[A/C]ATTTGACTCCATGCT | 81929 |
rs532762757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12966905 | ATCTCCCAGATCTCC[A/C]CTTTGTTCTCCAGGT | 81929 |
rs532808418 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SEH1L | GRCh38.p7 | 18:12954014 | CTTAGTGTGCATTTT[A/T]AATTTTATAGCCCTG | 81929 |
rs533059936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12954896 | ACCACCACCACTTCT[A/C]ATTTCAGAACATTGT | 81929 |
rs533183947 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12973063 | GTACAAAAATTAGCT[A/G]TGGGGATGATGGCGC | 81929 |
rs533261056 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SEH1L | GRCh38.p7 | 18:12981296 | TCCTCACTTCCCAGA[C/T]GGGGTGGCGGCCGGG | 81929 |
rs533261147 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12955950 | TCCTGGCCCCACCTC[A/G]GCCTCCTGAGTTGCT | 81929 |
rs533273051 | snp | A/G | | | intron-variant | SEH1L | GRCh38.p7 | 18:12976135 | TGTCTGTGGGTCAAG[A/G]GTCAGGCCAGACTGG | 81929 |
rs533298513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12983088 | TTCTCTGCAGCTCCC[A/G]TAAGTTAAGAGCCTT | 81929 |
rs533313467 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SEH1L | GRCh38.p7 | 18:12956294 | CGTGATCTGCCTGTC[A/G]GCCTCCCAAAGTGCT | 81929 |
rs533340886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SEH1L | GRCh38.p7 | 18:12977811 | AGAAAGATGTTAGTG[G/T]CTAATAAATCAAGCC | 81929 |