SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13723 | snp | C/T | 0.494774 | 0.0508504 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614868 | CTCCTGGGCTCAGGG[C/T]CCATCAGGCAGCCTC | 84940 |
rs871014 | snp | A/G | 0.494815 | 0.0506538 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618321 | GCTTATCCCAGCCGG[A/G]TGCCCTGGGAGGGCG | 84940 |
rs1064133 | snp | A/G | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614729 | TTTATTTGTGCCTCA[A/G]AATCAGTCTGGTGCC | 84940 |
rs2162660 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615271 | TTCCATCACCCTGAG[C/T]GGTAAACCAGATGGG | 84940 |
rs3029571 | in-del | -/ACAG | 0.0283406 | 0.115616 | intron-variant | CORO6 | GRCh38.p7 | 17:29616391 | CCCCCTTGGTCTTAG[-/ACAG]GAGAAGTTAAGGACG | 84940 |
rs3744628 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615527 | AGCCGAGTCCCAGAC[A/G]AGGCTCGCAGTCCAG | 84940 |
rs3760456 | snp | C/T | 0.463881 | 0.12944 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621826 | GCATCTCTTCACGGA[C/T]GTGGTTGTAGCTCCC | 84940 |
rs3809791 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618029 | GGCCAGGCCGCGCCG[G/T]GCGCGCTAGCTCGCT | 84940 |
rs3809792 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617127 | AGGGTTTGGGAAGGC[C/T]AGGAAGCGTAAAGGG | 84940 |
rs8065982 | snp | A/G | 0.0360663 | 0.129354 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614801 | GGGGGGAACGCCTAC[A/G]GTGTGGGTTGGGGTC | 84940 |
rs8075441 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | CORO6 | GRCh38.p7 | 17:29621031 | TAGGGAGTGGGAGTA[A/G]GCCACCCTGATGTTA | 84940 |
rs9889295 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622394 | CAGTGGCTCCTGCCC[A/C]ACCCCAGCCCCAGCA | 84940 |
rs9890056 | snp | A/C | 0.0468597 | 0.145719 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622750 | GAAGGGGCCCGAGTG[A/C]GTAGGGGGCCGAGGA | 84940 |
rs9894979 | snp | C/G/T | 0.0134861 | 0.0810011 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614787 | ACCTAACTTTACTTG[C/G/T]GGGGAACGCCTACGG | 84940 |
rs9900849 | snp | G/T | 0 | 0 | intron-variant | CORO6 | GRCh38.p7 | 17:29620897 | GGGATGCGGCATTAG[G/T]AGAGGCAGTGATGGA | 84940 |
rs9903385 | snp | C/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615310 | GCTGATTAGGAGAAG[C/G]GCTGTCATTTTCCCC | 84940 |
rs9910346 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621939 | ACAGGATACCGAACT[C/T]GCATCTCTGGAATAG | 84940 |
rs11540702 | snp | C/T | 0.0861826 | 0.188849 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615380 | TGATGCTTGGGGTTA[C/T]TGGAGCCTGAGCTTG | 84940 |
rs11553124 | snp | C/T | 0 | 0 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614728 | GGGCACCAGACTGAT[C/T]CTGAGGCACAAATAA | 84940 |
rs11650479 | snp | A/C | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619539 | GGGCAGGGCAGGGCC[A/C]TGGGACCCAGCACCT | 84940 |
rs11650514 | snp | A/C | 0.277778 | 0.248452 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619668 | TGATGGTGGTGTCGT[A/C]TGAGGCACTGGCGAT | 84940 |
rs11657079 | snp | C/T | 0.315719 | 0.241208 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617071 | GGAGGCGTGACCAGC[C/T]CTGCCCCACCCTCCC | 84940 |
rs11871271 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CORO6 | GRCh38.p7 | 17:29620407 | GAAAGAGCAGACATA[C/T]TGGGGGAGGAGGCAG | 84940 |
rs12162129 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29621114 | AGGAGCCAATCCACA[C/T]AGATGCTTCTCCTGA | 84940 |
rs12451014 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621760 | TTTTGGGAGGAGCCT[C/T]AATGCCACACTGCCT | 84940 |
rs34111908 | in-del | -/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620337 | TCTGAGACCTCTGCA[-/G]GGGCAGACACTGGTC | 84940 |
rs34262470 | in-del | -/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623873 | ACTTCCCACCCTCCA[-/G]GGCACACCTGGGAGT | 84940 |
rs35334517 | in-del | -/C | | | intron-variant, upstream-variant-2KB, synonymous-codon | CORO6 | GRCh38.p7 | 17:29618478 | CAGGAGCTCAGGTTT[-/C]ATGCAGGTTCTGGTG | 84940 |
rs36001900 | in-del | -/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614659 | GACACAAAGAGGGAT[-/G]GGAAGAAAAGAACAA | 84940 |
rs57737050 | snp | G/T | 0.0379877 | 0.132479 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624810 | GACAGTGCCACTTTA[G/T]CTCACAAGTGCTGAG | 84940 |
rs61732667 | snp | A/G | 0.0516902 | 0.152228 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618961 | CCAGATGATGATCAC[A/G]TTGTCACCACCTGCC | 84940 |
rs73280611 | snp | C/G | 0.0573587 | 0.15934 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615224 | CTCTGCAGCAAACGG[C/G]TTGTGTATGTGTCTG | 84940 |
rs77991986 | in-del | -/C | 0 | 0 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622916 | CCTAAGAGGGCGGGG[-/C]CTAGCATAGGGGCGG | 84940 |
rs79779927 | snp | C/T | 0.0524604 | 0.153226 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623311 | CCTAGAGAATGAGGA[C/T]CCAGGCTGATCCTGA | 84940 |
rs79996304 | snp | C/T | 0.0998734 | 0.199905 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614493 | GACTCTAAAACCCTT[C/T]ATCCAATGGTGCTAA | 84940 |
rs111487344 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614765 | CTTCATACCGGAGGC[G/T]TTTGCTACCTAACTT | 84940 |
rs111572312 | snp | A/G/T | 0 | 0 | splice-acceptor-variant | CORO6 | GRCh38.p7 | 17:29616338 | GTAGCTTGTAGAACC[A/G/T]ATAAGGGAGCAGGGT | 84940 |
rs112030766 | snp | A/G | | | splice-donor-variant | CORO6 | GRCh38.p7 | 17:29621222 | TTTCCCTGATCCCTC[A/G]CCTTGGCCAGAGGCA | 84940 |
rs112034012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO6 | GRCh38.p7 | 17:29620426 | GGGAGGAGGCAGCTC[C/T]GGCTGAAATTTGAGC | 84940 |
rs112317482 | snp | A/G/T | 7.88571e-05 | 0.00627872 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617578 | CTGGCGCGTGAAGAC[A/G/T]GCCCGCATGGGCCTC | 84940 |
rs112503922 | snp | C/T | | | splice-donor-variant | CORO6 | GRCh38.p7 | 17:29621223 | TTCCCTGATCCCTCA[C/T]CTTGGCCAGAGGCAG | 84940 |
rs113259900 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624304 | CCTCTAGGCTGGTCG[C/T]GGGTGGCTAACGCCT | 84940 |
rs113619334 | snp | C/T | 0.5 | 0 | intron-variant | CORO6 | GRCh38.p7 | 17:29621133 | TGCTTCTCCTGACTA[C/T]GGAATGGAACTAGGT | 84940 |
rs113697022 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623487 | CAGGAAGCAGCTGAA[A/G]GAACAAGGGGAGGAC | 84940 |
rs113833180 | snp | G/T | 0.444444 | 0.157135 | intron-variant | CORO6 | GRCh38.p7 | 17:29616511 | TGTTCACCATCATCT[G/T]ATAGATGAGGAAACT | 84940 |
rs114668106 | snp | A/G | 0.0205511 | 0.0992634 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621489 | AGTCCTGTGAGCTGC[A/G]GGAGGGAGGAGGAGT | 84940 |
rs114797199 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615121 | TTCGCGGGGGCTGCC[A/G]CGAGGAAGCAGCCCT | 84940 |
rs114944698 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CORO6 | GRCh38.p7 | 17:29620840 | CTTAATCAAATGGTC[A/C]TCTTGGGCTAGGGAG | 84940 |
rs115017679 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CORO6 | GRCh38.p7 | 17:29620943 | GCTGTGCTGTGTCCC[A/G]ACCATCTCCATCACC | 84940 |
rs117879473 | snp | G/T | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621501 | TGCGGGAGGGAGGAG[G/T]AGTGGAGGGGTGGCT | 84940 |
rs138126589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, synonymous-codon | CORO6 | GRCh38.p7 | 17:29618489 | GTTTCATGCAGGTTC[C/T]GGTGGGAGGATGGAG | 84940 |
rs138424174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619869 | GATTCCTTATTACCT[A/G]TTTTCTCTTTGCAGA | 84940 |
rs138692015 | snp | C/G | 0.00184279 | 0.0302985 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616077 | CCTCAGCGAAATGAG[C/G]ACGGGTTCGGCGTCC | 84940 |
rs139295677 | snp | G/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622149 | GAAGCCCTGATCATG[G/T]TCTTCTGGCTTTTGC | 84940 |
rs140098516 | snp | A/G | 0.0090587 | 0.066688 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615730 | CTGCCTGGCGCGCGG[A/G]GCTAGTCCGTGCCGT | 84940 |
rs140141463 | snp | A/C | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621821 | GATGAGCATCTCTTC[A/C]CGGACGTGGTTGTAG | 84940 |
rs140191201 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624601 | CACACGCACAAAAAA[A/C]CAAAAAACAATCCTC | 84940 |
rs141982268 | snp | A/C | 6.595e-05 | 0.00574201 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616788 | GCTGCTGAACGTGTT[A/C]AGGTAGTGCACGAAA | 84940 |
rs142109518 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621867 | TGTCCAGAAGCAGAA[A/G]ACTTGACCATTGGAT | 84940 |
rs142118749 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619309 | AAGGGTCAAATACAG[A/G]GCAAGATGTGGTGGT | 84940 |
rs142182145 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623862 | GGCCAGTTATTACTT[C/T]CCACCCTCCAGGGCA | 84940 |
rs142704020 | snp | C/T | 3.465e-05 | 0.00416219 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616097 | GTTCGGCGTCCTGGC[C/T]GGATAGCCATTCGTC | 84940 |
rs143051080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620959 | ACCATCTCCATCACC[C/T]GGCTCCCCTCCTGGT | 84940 |
rs143699377 | snp | A/G | 0.0353628 | 0.128183 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616006 | GGCGGGCGCACGTCC[A/G]GGATGTTGCGCTTCG | 84940 |
rs144430370 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619992 | GAGAGGTAAGATGGC[C/T]TCATCAAGGACACAC | 84940 |
rs145189449 | snp | A/C/G/T | 0.00221707 | 0.033225 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622893 | AGCCCCAGCTGCCGC[A/C/G/T]GCCATCAACCTAAGA | 84940 |
rs145299989 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623510 | GGGAGGACCGAGTGT[A/T]AAGTGAACCCACCTT | 84940 |
rs145891968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619848 | TAGCAGATCTGCTTA[C/T]ATCTCGATTCCTTAT | 84940 |
rs145924561 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624053 | GTCAGTGGCTTGTAG[A/G]GGAACAGAATAAAAA | 84940 |
rs146122207 | snp | A/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615451 | AAGGGGGACACCACC[A/T]CGCCGTGCAGCACCA | 84940 |
rs146140978 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621648 | AATGCTGTTTAATGT[A/G]AGTGGCTAGGATTTG | 84940 |
rs146808043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616409 | TCTAAGACCAAGGGG[G/T]TTGGAGGCCAACACT | 84940 |
rs146919004 | snp | A/C | 1.7074e-05 | 0.00292177 | missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616124 | CGTCCGCTTCTAGGG[A/C]CGGCTCCGGGCCTGG | 84940 |
rs146995190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618306 | CGAGGCCAGGGCCGC[C/T]GCCCTCCCAGGGCAT | 84940 |
rs147633307 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623830 | GATTTCTTCCCTTGG[A/G]TCATAAGGGCATCTG | 84940 |
rs148179219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620682 | CCCATCCTGAGGGTA[A/G]GGAGGGCTCTGGCTT | 84940 |
rs148707315 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623111 | GGGGAGGCTCGGGTT[A/C]GCAGACCTAGAGCAG | 84940 |
rs149253472 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619974 | ATTAGGGACTGTGAC[A/G]CAGAGAGGTAAGATG | 84940 |
rs149562910 | in-del | -/AG | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615161 | CGGTGGAAAGAAGGA[-/AG]AGAGTTCTCTACCAC | 84940 |
rs150675943 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616847 | GAATGCTGCTGTCGC[C/T]CTGCAAAATCAGTCG | 84940 |
rs150860766 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622097 | AGAGTGAGGTGGATC[C/G]CTCTTCTCCCACTCC | 84940 |
rs150908445 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615033 | TCTGAGAGAGGCAAC[A/G]GCAGAGGGTTGGGGG | 84940 |
rs151176506 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624113 | TGGCGTAGGGGTGCT[A/G]GGGCAGGGTATGAGG | 84940 |
rs151229946 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617809 | CCTGGAGAGCATCCG[A/G]GCCTGGAGAGAGCAG | 84940 |
rs181260808 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621905 | TAAAGCCAGGTATGG[A/G]GCCAAGACTGCAGCC | 84940 |
rs182101059 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624485 | CAGGAGGCTGAGACA[C/T]GAGAATTGCTTGAAC | 84940 |
rs182725588 | snp | A/C | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617424 | GGTGGGCATGCCCTG[A/C]GGGTGGGGGGCGCCT | 84940 |
rs183210181 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624850 | AACTGAGAGTTTATA[C/T]TGTGTGGCACAGAGG | 84940 |
rs183288956 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614745 | TGAGGCACAAATAAA[A/C]GAGGCTTCATACCGG | 84940 |
rs183962792 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623863 | GCCAGTTATTACTTC[C/T]CACCCTCCAGGGCAC | 84940 |
rs183984079 | snp | C/G | 0.000121308 | 0.00778711 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615930 | TGGGCCAGAGTGCAG[C/G]AGGGCCGATCTTACC | 84940 |
rs184625815 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29620053 | CTTTCCAGCCCAGTG[C/G]TCTTCCAAAGACACC | 84940 |
rs185353317 | snp | A/G | 0.000149911 | 0.00865639 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618756 | CTGGCCACTGGTCAA[A/G]GGGTTCTGGGGAGTG | 84940 |
rs185519746 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CORO6 | GRCh38.p7 | 17:29620636 | AAGGGGCTTAAGGTT[A/T]TGAAGCTAACGTGGT | 84940 |
rs186320722 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624102 | GAAATAACTCCTGGC[A/G]TAGGGGTGCTGGGGC | 84940 |
rs186784044 | snp | C/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624785 | CATGCATTTCTGTCT[C/G]TCCCTGAAGGACAGT | 84940 |
rs186893482 | snp | A/C | 0.00062072 | 0.0176061 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615935 | CAGAGTGCAGCAGGG[A/C]CGATCTTACCGACAA | 84940 |
rs186906344 | snp | A/G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622933 | TAGCATAGGGGCGGG[A/G/T]CCAGAGCCCAAGTTG | 84940 |
rs187008656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617676 | CTGCCCTGAGGAGCA[C/T]GGAGGGATGAGCAAC | 84940 |
rs187417457 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615166 | GAAAGAAGGAAGAGA[A/G]TTCTCTACCACAGAC | 84940 |
rs188248233 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620253 | GCAAGCAGTCCTGGT[A/G]CCTACTATCCCCAAA | 84940 |
rs189396265 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621733 | CTGAAAGCTTTCTGG[A/T]CGTTGGAATGTTTTT | 84940 |
rs189881050 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624287 | TTCATACTCTTAACA[A/G]TCCTCTAGGCTGGTC | 84940 |
rs190204003 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619363 | GGGAGCCAGGAGGGG[C/G]CACTGCCAGCTCTCC | 84940 |
rs191308299 | snp | A/G | | | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616286 | CCCCTCACCTTGCGG[A/G]GCACAGTCATGATGA | 84940 |
rs191739451 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623533 | CCCACCTTGACACTC[C/T]CTCCCCTCCCAGATG | 84940 |
rs192086816 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615196 | CCGCTGTGGGTGTAG[C/T]CACTGGGTCCGGCTC | 84940 |
rs192786211 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624832 | AGTGCTGAGCTAAAA[C/T]GTAACTGAGAGTTTA | 84940 |
rs193135655 | snp | C/G | 1.66161e-05 | 0.00288232 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619778 | ACTCGCCCTGTCTGA[C/G]GGGTTGGAGAAGAAG | 84940 |
rs193156938 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617847 | GCGGCTCTCAGCCGA[C/T]CCCGAACCCTTAAGC | 84940 |
rs199548298 | snp | C/G | 1.70592e-05 | 0.0029205 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616138 | GCCGGCTCCGGGCCT[C/G]GCGTATCCGGGTACA | 84940 |
rs200010729 | snp | A/C/G | 1.64887e-05 | 0.00287125 | missense, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616785 | TTTGCTGCTGAACGT[A/C/G]TTCAGGTAGTGCACG | 84940 |
rs200229530 | snp | A/G | 0.000529507 | 0.0162626 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621412 | TTTGCCGAACCACAC[A/G]TCTGCTCATAGCTGC | 84940 |
rs200293727 | snp | A/G | 0.000247245 | 0.0111158 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616982 | CGGGATCGTAAAAGG[A/G]CAATAGGACCCCGTT | 84940 |
rs200487393 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617158 | ATGCCCCAAACCTCT[A/G]GTGACCAGAGTTGCA | 84940 |
rs200504173 | snp | A/G | 0.000372255 | 0.0136378 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617602 | GGGCCTCATCCCCTC[A/G]TGGGCCGCAAACCTC | 84940 |
rs200773299 | snp | C/G/T | 0.000154419 | 0.00878563 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616109 | GGCCGGATAGCCATT[C/G/T]GTCCGCTTCTAGGGC | 84940 |
rs201030691 | snp | A/C/G/T | 0.00165599 | 0.0287282 | intron-variant | CORO6 | GRCh38.p7 | 17:29616655 | GGACCCGACATGAGT[A/C/G/T]GGGGACAGAGGCGGG | 84940 |
rs201055158 | snp | C/T | 1.81625e-05 | 0.00301346 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617480 | CCGAGGCACACACCC[C/T]AAGCCTCCAGCTGCG | 84940 |
rs201079237 | snp | G/T | 0.000585651 | 0.0171021 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615739 | GCGCGGGGCTAGTCC[G/T]TGCCGTCCACCAGCT | 84940 |
rs201101451 | snp | A/G | | | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616087 | ATGAGCACGGGTTCG[A/G]CGTCCTGGCCGGATA | 84940 |
rs201216186 | snp | G/T | 0.000179822 | 0.00948044 | stop-gained, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616069 | TAGCCGTCCCTCAGC[G/T]AAATGAGCACGGGTT | 84940 |
rs201236237 | snp | A/G | 0.000196515 | 0.00991053 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617502 | CCAGCTGCGTTACCG[A/G]GTCCCACAGGCCCAG | 84940 |
rs201402766 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619259 | CACTCCTTCCCTACC[-/T]TTTTTTTTTAACCCT | 84940 |
rs201413487 | snp | A/G | 3.84061e-05 | 0.00438196 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615906 | GGGGCGGTTGGGGGA[A/G]ATGTAGATTGGGCCA | 84940 |
rs201440567 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621347 | CACACGGATGTCCTC[A/G]TAGGCCTGGTCGGCC | 84940 |
rs201494980 | snp | C/G | 0.00399205 | 0.0444982 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617248 | CACATATACCCGCTG[C/G]GCGCCGCATGCAGTC | 84940 |
rs201624665 | snp | A/T | 0.00018232 | 0.00954603 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619656 | TGGCTCCTACCATGA[A/T]GGTGGTGTCGTCTGA | 84940 |
rs201736872 | snp | C/G | 0.000255896 | 0.0113085 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616132 | TCTAGGGCCGGCTCC[C/G]GGCCTGGCGTATCCG | 84940 |
rs201898206 | snp | A/C | 4.94539e-05 | 0.00497238 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616964 | GGTAGACGATGCTGG[A/C]GTCGGGATCGTAAAA | 84940 |
rs201994744 | snp | C/T | 4.01139e-05 | 0.00447832 | intron-variant | CORO6 | GRCh38.p7 | 17:29616266 | CTGCCCAACCCTTCT[C/T]CCGGCCCCTCACCTT | 84940 |
rs201995220 | snp | A/G | 1.66438e-05 | 0.00288472 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619796 | GTTGGAGAAGAAGAT[A/G]TGGGGCTACTCTCCT | 84940 |
rs202223489 | snp | A/C/T | 0.000117419 | 0.00766132 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615784 | TCCAGAGCCGTGATG[A/C/T]GCTGCTCCTGGGCCT | 84940 |
rs207476356 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619117 | GGATGCCCACACGCT[C/T]GGAGTGGCCCTCAAG | 84940 |
rs367556536 | snp | A/C | 0.000949217 | 0.0217648 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619070 | CAGACCTGCACTGAG[A/C]AGGACATTCCTGGCA | 84940 |
rs367821219 | snp | A/G | 0.000103704 | 0.00720009 | synonymous-codon, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616170 | ATCGTCCTGGAAGAG[A/G]TCTGACTGCGGGGGT | 84940 |
rs367948668 | snp | A/G | 1.66863e-05 | 0.0028884 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619134 | GAGTGGCCCTCAAGT[A/G]TGATGATAGGTTCCG | 84940 |
rs368243534 | snp | C/T | 3.29821e-05 | 0.00406078 | intron-variant | CORO6 | GRCh38.p7 | 17:29616918 | CCAGTGCCCTGTTCT[C/T]CCTGCCCGGCCGTGA | 84940 |
rs368519460 | snp | C/T | 1.72154e-05 | 0.00293384 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619239 | TGAGGAGCCACCCTG[C/T]CCCTCCACTCCTTCC | 84940 |
rs368592581 | snp | C/T | 1.68029e-05 | 0.00289848 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621346 | ACACACGGATGTCCT[C/T]GTAGGCCTGGTCGGC | 84940 |
rs368623066 | snp | A/C/T | 0.000247971 | 0.0111326 | intron-variant | CORO6 | GRCh38.p7 | 17:29616378 | TCGCAGACTTCCACG[A/C/T]CCTTAACTTCTCCTG | 84940 |
rs368961234 | snp | C/T | 0.000311951 | 0.0124851 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618913 | TGGGTGCATATCATC[C/T]AGGCTCAGCAGCACC | 84940 |
rs369836156 | snp | A/G | 0.000359002 | 0.013393 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618750 | TGACAGCTGGCCACT[A/G]GTCAAGGGGTTCTGG | 84940 |
rs370213136 | snp | A/G | 0.000530725 | 0.0162813 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615904 | TAGGGGCGGTTGGGG[A/G]AGATGTAGATTGGGC | 84940 |
rs370298559 | snp | A/G | 0.000159987 | 0.00894249 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619073 | ACCTGCACTGAGCAG[A/G]ACATTCCTGGCAGTA | 84940 |
rs370360290 | snp | C/T | 0.000155054 | 0.00880357 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616052 | GGTGCTTGGGGGGCA[C/T]ATAGCCGTCCCTCAG | 84940 |
rs370489778 | snp | A/G | 0.000187315 | 0.00967587 | intron-variant | CORO6 | GRCh38.p7 | 17:29616214 | GACTTGCGTGAGAGG[A/G]TGCGGGGCTTGCTCC | 84940 |
rs370893604 | snp | A/G | 0.0001998 | 0.00999301 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618997 | TGGCCAGGCATGGTC[A/G]CCTGGGTCCCACCTT | 84940 |
rs371000206 | snp | A/C | 3.33344e-05 | 0.00408241 | splice-donor-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619059 | TCCTTAGCCCCCAGA[A/C]CTGCACTGAGCAGGA | 84940 |
rs371062707 | snp | A/C/T | 0.00151355 | 0.0274682 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619224 | ATATGGTGGGTGGAA[A/C/T]GAGGAGCCACCCTGT | 84940 |
rs371210343 | snp | A/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621360 | TCGTAGGCCTGGTCG[A/G]CCTTTGCTGCCTGCC | 84940 |
rs371297059 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621902 | GCTTAAAGCCAGGTA[C/T]GGGGCCAAGACTGCA | 84940 |
rs371328329 | snp | C/T | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617855 | CAGCCGATCCCGAAC[C/T]CTTAAGCGCGCTCAA | 84940 |
rs371388900 | snp | C/T | 9.95768e-05 | 0.00705539 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621411 | CTTTGCCGAACCACA[C/T]GTCTGCTCATAGCTG | 84940 |
rs371900852 | snp | A/T | 1.81187e-05 | 0.00300982 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617482 | GAGGCACACACCCCA[A/T]GCCTCCAGCTGCGTT | 84940 |
rs371963989 | snp | C/G | 1.65312e-05 | 0.00287495 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617060 | GCCCGAGCACAGGAG[C/G]CGTGACCAGCCCTGC | 84940 |
rs372167192 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620966 | CCATCACCCGGCTCC[C/T]CTCCTGGTCCCTGCT | 84940 |
rs372204134 | snp | C/T | 0.00125224 | 0.0249911 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619147 | GTGTGATGATAGGTT[C/T]CGTAATGTTGCGCAT | 84940 |
rs372494637 | snp | A/G | 0.000215323 | 0.0103738 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619681 | GTCTGAGGCACTGGC[A/G]ATAACGTTGTCATTG | 84940 |
rs372595207 | snp | C/G | 7.97162e-05 | 0.00631282 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615743 | GGGGCTAGTCCGTGC[C/G]GTCCACCAGCTCGCA | 84940 |
rs372681638 | snp | C/T | 3.31923e-05 | 0.0040737 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618933 | TCAGCAGCACCTCCC[C/T]GGTGCCCACATTCCA | 84940 |
rs372891094 | snp | A/C/G | 0.000221263 | 0.0105158 | intron-variant | CORO6 | GRCh38.p7 | 17:29616385 | CTTCCACGTCCTTAA[A/C/G]TTCTCCTGTCTAAGA | 84940 |
rs373085942 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615115 | GATTTCTTCGCGGGG[A/G]CTGCCGCGAGGAAGC | 84940 |
rs373096545 | snp | A/C/T | 1.66765e-05 | 0.00288756 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619015 | TGGGTCCCACCTTTG[A/C/T]CACCACCCACCCATC | 84940 |
rs373123604 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618352 | AACGCGCGAGGGTTG[C/G]CCCATCCCCCGCCCA | 84940 |
rs373788306 | snp | C/T | 7.59417e-05 | 0.00616158 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615899 | TCGTATAGGGGCGGT[C/T]GGGGGAGATGTAGAT | 84940 |
rs373980692 | snp | C/G | 0.000159987 | 0.00894249 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618787 | GCCAGGCCAGGCACT[C/G]ACCGCCACCACTTGG | 84940 |
rs374236088 | snp | C/G | 0.000130745 | 0.00808426 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622820 | AGTATCTGGGACCCG[C/G]GTGTCCAGCTCCGCA | 84940 |
rs374276508 | snp | A/G | 1.96783e-05 | 0.00313668 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621388 | GCCCAAACACATGGC[A/G]GAACTTGCTTTGCCG | 84940 |
rs374517928 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615630 | CCCCAGTCCCGCCCC[C/T]GGGCCCAGCCCAAGA | 84940 |
rs374753616 | snp | A/G | 0.000247392 | 0.0111191 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616284 | GGCCCCTCACCTTGC[A/G]GGGCACAGTCATGAT | 84940 |
rs374807611 | snp | C/T | 0.000159987 | 0.00894249 | intron-variant | CORO6 | GRCh38.p7 | 17:29621202 | GTGTCCTCCCACTTG[C/T]TTCCTTTCCCTGATC | 84940 |
rs375005683 | snp | C/T | 1.66593e-05 | 0.00288607 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619081 | TGAGCAGGACATTCC[C/T]GGCAGTAGGGTGCCA | 84940 |
rs375336485 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO6 | GRCh38.p7 | 17:29621003 | GGGGTGGTGCATGGA[C/G]AGGTGGGAGGGCTAG | 84940 |
rs375419798 | snp | C/T | 6.62614e-05 | 0.00575554 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619680 | CGTCTGAGGCACTGG[C/T]GATAACGTTGTCATT | 84940 |
rs375463631 | snp | A/C/G | 5.01872e-05 | 0.00500914 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619159 | GTTCCGTAATGTTGC[A/C/G]CATGGGGGTATAGTC | 84940 |
rs375589228 | snp | A/G | 0.000870847 | 0.0208486 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619169 | GTTGCGCATGGGGGT[A/G]TAGTCTGGAATCTGC | 84940 |
rs375611970 | snp | C/T | 0.000157988 | 0.00888644 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618824 | CTGGGGTCAATGATG[C/T]GCAAGGTCTTGTCCT | 84940 |
rs375954735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617882 | TCAAAGGCCGATCCC[C/T]AGAGCAGGGGTGTCT | 84940 |
rs376581271 | snp | A/G/T | 7.33629e-05 | 0.00605616 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617622 | CCGCAAACCTCTCCT[A/G/T]GGGGGAGGGGGAGAC | 84940 |
rs376655912 | snp | A/G | 3.4522e-05 | 0.00415449 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621359 | CTCGTAGGCCTGGTC[A/G]GCCTTTGCTGCCTGC | 84940 |
rs376958047 | snp | G/T | 0.000155988 | 0.00883005 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615902 | TATAGGGGCGGTTGG[G/T]GGAGATGTAGATTGG | 84940 |
rs377003436 | snp | C/T | 0.000930418 | 0.0215486 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615764 | CCAGCTCGCACAGCA[C/T]GTTCTCCAGAGCCGT | 84940 |
rs377223092 | snp | A/C/G/T | 0.000165019 | 0.00908216 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616744 | AGTCCCCTTTTGGGC[A/C/G/T]TGAAACCCATGCCCC | 84940 |
rs377380391 | snp | A/G | 0.000161987 | 0.00899819 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619032 | ACCACCCACCCATCT[A/G]TGGGGGACCCCTCCT | 84940 |
rs377722229 | snp | C/T | 0.000114523 | 0.00756625 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621402 | CGGAACTTGCTTTGC[C/T]GAACCACACGTCTGC | 84940 |
rs386385872 | in-del | -/C | 0 | 0 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622917 | CTAAGAGGGCGGGGC[-/C]TAGCATAGGGGCGGG | 84940 |
rs527374273 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622283 | CCCTGCCCCCGCCAC[A/G]GCCAAGCCAGATTTG | 84940 |
rs527381247 | snp | G/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619499 | GGGAGGGGGTGGGCA[G/T]GTAGCTAAAAATAGT | 84940 |
rs527420792 | snp | A/C/T | 0.000298686 | 0.0122169 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622864 | TGCGGCTCTCTAGAG[A/C/T]CCGGCGCCGCTGCAG | 84940 |
rs527482000 | snp | G/T | 0.00997481 | 0.0699136 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622674 | GTGACGGCCGGGTGT[G/T]GGGGGCTGGGTACCT | 84940 |
rs527841317 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615629 | TCCCCAGTCCCGCCC[C/G]CGGGCCCAGCCCAAG | 84940 |
rs528223027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, synonymous-codon | CORO6 | GRCh38.p7 | 17:29618570 | CTTCTGAGATGCAAG[A/G]GAGGGGAGGGAACAG | 84940 |
rs528781661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619583 | CCTTAGCACCTTCCC[C/T]AGCACAGGTGAGGCA | 84940 |
rs528910705 | snp | G/T | 4.94792e-05 | 0.00497365 | intron-variant | CORO6 | GRCh38.p7 | 17:29616856 | TGTCGCCCTGCAAAA[G/T]CAGTCGGTTCAGGGG | 84940 |
rs529028062 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CORO6 | GRCh38.p7 | 17:29616600 | ATCCCCCCGCCCCGC[-/T]TTTCCAAAGCACTGC | 84940 |
rs529188673 | snp | A/G | 0.000877578 | 0.0209289 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622944 | CGGGGCCAGAGCCCA[A/G]GTTGCCCCGCCCCCT | 84940 |
rs529384365 | snp | A/C/T | 0.000644538 | 0.0179403 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617999 | GGAAGGCGCTCCCGG[A/C/T]AGACCCAGAGAAGGA | 84940 |
rs529600965 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623609 | CAGAGAAGCCAACTC[A/G]GAGGCCAGACTCCTA | 84940 |
rs530573903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617183 | GTTGCAGGCCCCTCC[C/G]CTGGGCACATCTCTC | 84940 |
rs530948513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620366 | TCCAGACCAGGCAGC[A/G]GGGGAGAGGGTGGCT | 84940 |
rs531226256 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615738 | CGCGCGGGGCTAGTC[C/G]GTGCCGTCCACCAGC | 84940 |
rs531479120 | snp | A/G | 1.70699e-05 | 0.00292142 | synonymous-codon, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616149 | GCCTGGCGTATCCGG[A/G]TACAGATCGTCCTGG | 84940 |
rs531677042 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622377 | ACTCCCAAAGCCCCA[G/T]CCAGTGGCTCCTGCC | 84940 |
rs532675065 | snp | C/T | 3.86205e-05 | 0.00439417 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621384 | GCCTGCCCAAACACA[C/T]GGCGGAACTTGCTTT | 84940 |
rs532707443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620556 | ACAAGGTGTAGGGGC[C/T]AGAATCCAGGTCAAG | 84940 |
rs532832412 | snp | C/T | 0.00458952 | 0.0476833 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622760 | GAGTGCGTAGGGGGC[C/T]GAGGAAGGCTTCAGG | 84940 |
rs532949055 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624187 | GATTAGGAGGAAAAT[A/G]CCTGAGTGACTCAGT | 84940 |
rs533247552 | snp | A/T | 0.000156698 | 0.00885011 | intron-variant | CORO6 | GRCh38.p7 | 17:29616353 | TATAAGGGAGCAGGG[A/T]TCAGCACCCTCGCAG | 84940 |
rs533449677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618717 | CAGGGGCTCTGATAA[C/T]GGTGGGTACAAGGGT | 84940 |
rs533617237 | snp | G/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615090 | TAACTCCTCATGCCA[G/T]TTCTCTCGAGATTTC | 84940 |
rs533627149 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614284 | TGTCCAACGTAGCCC[C/T]CTGGCCTGTGCAAGC | 84940 |
rs533746339 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621686 | AATTCTCCACAGAGA[C/T]CCAGGCTGAGGGGAT | 84940 |
rs533839126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620853 | TCATCTTGGGCTAGG[C/G]AGGAGGTTCTCCACA | 84940 |
rs534027948 | snp | C/G | 0.000176258 | 0.00938605 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622718 | CTGCGGGGCGCTCAC[C/G]CTGCGAATCCTCTGC | 84940 |
rs534304245 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623078 | TGCTTCCCTCCCTCC[A/G]TGACTCCCGGGTAGG | 84940 |
rs534717231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618358 | CGAGGGTTGCCCCAT[C/T]CCCCGCCCAGCGGGT | 84940 |
rs535204257 | snp | A/C | 1.66189e-05 | 0.00288256 | splice-acceptor-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618972 | TCACATTGTCACCAC[A/C]TGCCCAGAGTGGCCA | 84940 |
rs535423984 | in-del | -/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624437 | CAAAAATTTGCCAGG[-/T]TGTGGTGATGCACAC | 84940 |
rs535431920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616488 | TGCAATAAAACACCC[C/T]GATGGTGTGTTCACC | 84940 |
rs535541264 | snp | C/G | 0.000763504 | 0.0195236 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617301 | TCGGCATCACCAGGT[C/G]GGGGCGCCAGCGCAG | 84940 |
rs535619137 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622559 | TGTCCGGCCAAATAT[A/T]GACACCACGTCCTCC | 84940 |
rs535722916 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615255 | CAGAACTGGGGTGAC[A/G]CCCATCTGGTTTACC | 84940 |
rs535747798 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620889 | AACATGAGGGGATGC[A/G]GCATTAGGAGAGGCA | 84940 |
rs535748465 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624431 | AAAAATACAAAAATT[G/T]GCCAGGTGTGGTGAT | 84940 |
rs535809513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619832 | TTTTTTGGGGAGTGG[A/G]TAGCAGATCTGCTTA | 84940 |
rs535979732 | in-del | -/C | 0.00676609 | 0.0577691 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624721 | GTAGTTGATGTAGCT[-/C]ATGATTCTTACCCAC | 84940 |
rs536744987 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621861 | GCACCCTGTCCAGAA[G/T]CAGAAGACTTGACCA | 84940 |
rs537324262 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622004 | TTTGCCAAGGGGGAA[G/T]TTCCTCCTGTCCACC | 84940 |
rs537727247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618294 | ACTTGAGGCTGGCGA[G/T]GCCAGGGCCGCCGCC | 84940 |
rs537793790 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614443 | TGCTGCTAGCCTCTG[C/T]GGTTGTACATCCCAC | 84940 |
rs538399226 | snp | A/T | 1.6566e-05 | 0.00287797 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619740 | GGGCAGTGTGCCCAG[A/T]GACCAGTGGGTAGTT | 84940 |
rs539421172 | snp | A/T | 0.000524797 | 0.0161902 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618119 | GCTTCCCGTCTGCGG[A/T]GAAGACAGCCCGCAG | 84940 |
rs539614410 | snp | C/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615980 | CCGACTGGCTGCGGC[C/G]GGGGCCGGAGGGCGG | 84940 |
rs540070509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619281 | TTTAACCCTACTGGC[G/T]CTCTTGAGTGGTAAG | 84940 |
rs540588093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29621171 | AAGGCTCAGGAGTTC[C/T]CAGGGGCCCCAGCTA | 84940 |
rs540652429 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621949 | GAACTCGCATCTCTG[C/G]AATAGTTCAGGCAGA | 84940 |
rs540724570 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614902 | ATCGCCAGGTCTCCC[A/G]GGAGCCTGGGGGTAG | 84940 |
rs540771017 | snp | C/T | 1.79187e-05 | 0.00299317 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622706 | GTCCTGAGCGGGCTG[C/T]GGGGCGCTCACGCTG | 84940 |
rs541061536 | snp | C/G/T | 3.29898e-05 | 0.00406128 | intron-variant | CORO6 | GRCh38.p7 | 17:29616872 | CAGTCGGTTCAGGGG[C/G/T]GCGCCCGGACAAGGC | 84940 |
rs541119999 | snp | A/G | 0.00114325 | 0.0238813 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617345 | ACGCAGCAAAACTGG[A/G]CAGAGGGGTGGGTGT | 84940 |
rs541124891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617774 | ACTCAGCTTCCTGCG[G/T]GGCCACGTCTGGCCC | 84940 |
rs541334753 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624878 | AGGAAAGGATGCCTG[A/G]AATGAATTAAAAAAC | 84940 |
rs541540064 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622182 | ACCATAGGCTTGTCC[A/G]GTTTCTCCTCTGGGT | 84940 |
rs542021421 | snp | A/G/T | 1.66983e-05 | 0.00288944 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619139 | GCCCTCAAGTGTGAT[A/G/T]ATAGGTTCCGTAATG | 84940 |
rs542106614 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623593 | GTCACATTTTAGGGG[G/T]CAGAGAAGCCAACTC | 84940 |
rs542114976 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615524 | TCCAGCCGAGTCCCA[G/T]ACGAGGCTCGCAGTC | 84940 |
rs542127255 | snp | A/T | 0.000399281 | 0.0141238 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616055 | GCTTGGGGGGCACAT[A/T]GCCGTCCCTCAGCGA | 84940 |
rs542512505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | CORO6 | GRCh38.p7 | 17:29618515 | TGGAGTTTCCAGCTT[C/T]TCCCCTCCTCAATCC | 84940 |
rs542804592 | snp | A/G | 0.000150161 | 0.00866361 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622867 | GGCTCTCTAGAGCCC[A/G]GCGCCGCTGCAGCCC | 84940 |
rs543070377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620368 | CAGACCAGGCAGCGG[A/G]GGAGAGGGTGGCTAT | 84940 |
rs543132922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29621030 | CTAGGGAGTGGGAGT[A/T]AGCCACCCTGATGTT | 84940 |
rs543140429 | snp | A/G | 1.76033e-05 | 0.00296671 | intron-variant | CORO6 | GRCh38.p7 | 17:29616180 | AAGAGGTCTGACTGC[A/G]GGGGTGGGTGGACAG | 84940 |
rs543480611 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624019 | CCAGGTGGCTTGTAG[G/T]GACAGAATCAAATCA | 84940 |
rs543823447 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621526 | GTGGCTGATGAGAAG[A/G]GTTATGTGGTCAGGA | 84940 |
rs544514166 | snp | G/T | 0.00168985 | 0.0290185 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622748 | CGGAAGGGGCCCGAG[G/T]GCGTAGGGGGCCGAG | 84940 |
rs544560289 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615444 | GAGGACAAAGGGGGA[C/T]ACCACCTCGCCGTGC | 84940 |
rs544576313 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622092 | AGCACAGAGTGAGGT[A/G]GATCCCTCTTCTCCC | 84940 |
rs544645896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618423 | TCAGGCCCCAGACCC[C/T]GGAAGATGCGTCTGG | 84940 |
rs545293072 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617820 | TCCGGGCCTGGAGAG[A/T]GCAGGAGGCACGCGG | 84940 |
rs545475422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619323 | GGGCAAGATGTGGTG[A/G]TGCATGCCTAGAACA | 84940 |
rs545503072 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616987 | TCGTAAAAGGGCAAT[A/G]GGACCCCGTTGCTTG | 84940 |
rs546166170 | snp | A/G | | | intron-variant, upstream-variant-2KB, synonymous-codon | CORO6 | GRCh38.p7 | 17:29618591 | GAGGGAACAGGAGCC[A/G]GGCAGAGAATTGCAG | 84940 |
rs546908504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619584 | CTTAGCACCTTCCCC[A/G]GCACAGGTGAGGCAG | 84940 |
rs547009004 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615296 | ATGGAATCCAGTGAG[A/C]TGATTAGGAGAAGCG | 84940 |
rs547046363 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619839 | GGGAGTGGGTAGCAG[A/G]TCTGCTTACATCTCG | 84940 |
rs547266214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620463 | GCTGTGTCCCAGGAT[A/G]ATGTCTGCATTGTCT | 84940 |
rs547418052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617425 | GTGGGCATGCCCTGC[G/T]GGTGGGGGGCGCCTG | 84940 |
rs547496704 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615533 | GTCCCAGACGAGGCT[C/T]GCAGTCCAGCCTCCG | 84940 |
rs547505299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, synonymous-codon | CORO6 | GRCh38.p7 | 17:29618585 | GGAGGGGAGGGAACA[A/G]GAGCCGGGCAGAGAA | 84940 |
rs547654568 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623050 | TGTGCAGCTGTGTGC[C/T]AGGTGCGCACGCTGC | 84940 |
rs547666853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624150 | GAGTCATCTCTCTTT[C/T]ACCTAAAGATTCCAG | 84940 |
rs547733920 | snp | C/G/T | 0.000195903 | 0.00989525 | intron-variant | CORO6 | GRCh38.p7 | 17:29616238 | TTGCTCCGCTCCCTT[C/G/T]CGCCTCGTAGCCCTG | 84940 |
rs547822831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620688 | CTGAGGGTAGGGAGG[A/G]CTCTGGCTTTATGTG | 84940 |
rs547834991 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621622 | TATGGGAAAGTTATT[C/T]TGCTGTGTAAAATGC | 84940 |
rs548008465 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614566 | ACAGACCCCGCCAGG[A/G]GCAGGGGCCCACCGC | 84940 |
rs548409211 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615125 | CGGGGGCTGCCGCGA[A/G]GAAGCAGCCCTCGCC | 84940 |
rs548802609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617898 | AGAGCAGGGGTGTCT[C/G]CTGGCTCCCCGGAGT | 84940 |
rs548956958 | snp | G/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620140 | TCCTGGTGGAAGAGG[G/T]CAAGGTGAGATAATA | 84940 |
rs549404523 | snp | A/C | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624117 | GTAGGGGTGCTGGGG[A/C]AGGGTATGAGGGTAT | 84940 |
rs549658146 | snp | A/C | 1.67421e-05 | 0.00289323 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618827 | GGGTCAATGATGCGC[A/C]AGGTCTTGTCCTTGC | 84940 |
rs549773249 | snp | A/G | 0.000141834 | 0.00842003 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615758 | CGTCCACCAGCTCGC[A/G]CAGCATGTTCTCCAG | 84940 |
rs549802836 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624310 | GGCTGGTCGCGGGTG[A/G]CTAACGCCTGTAATC | 84940 |
rs549831876 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615227 | TGCAGCAAACGGGTT[G/T]TGTATGTGTCTGCAG | 84940 |
rs550051066 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622503 | CTGACACTGCGTTCT[A/T]GCGAGACGAGGTGTC | 84940 |
rs550098545 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620552 | CCTAACAAGGTGTAG[A/G]GGCCAGAATCCAGGT | 84940 |
rs550124163 | snp | A/G | 0.000220192 | 0.0104903 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622897 | CCAGCTGCCGCTGCC[A/G]TCAACCTAAGAGGGC | 84940 |
rs550272643 | snp | C/T | 8.79546e-05 | 0.00663096 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617196 | CCCCTGGGCACATCT[C/T]TCCTCCTCCCCTGCG | 84940 |
rs551512838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618722 | GCTCTGATAATGGTG[A/G]GTACAAGGGTGCTGA | 84940 |
rs551582326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616369 | TCAGCACCCTCGCAG[A/G]CTTCCACGTCCTTAA | 84940 |
rs552065381 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618215 | GGCGCCAGCCCCGAC[A/C/T]GCTCTCGGCGCGCTT | 84940 |
rs552184277 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622327 | GGTGAGGTGCCTTTT[C/T]TCCAGCTAGGGTCTC | 84940 |
rs552660905 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624254 | GGCACTGGCACTAAG[A/G]GCTTTATACGTATTA | 84940 |
rs553058746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618373 | CCCCCGCCCAGCGGG[C/T]CCACAAGGAGAAAGG | 84940 |
rs553991154 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622619 | GGGAGGAGGCGCAGA[A/C]CTCTGCCCCTCAGGG | 84940 |
rs554000087 | snp | C/G/T | 5.41261e-05 | 0.00520198 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616068 | ATAGCCGTCCCTCAG[C/G/T]GAAATGAGCACGGGT | 84940 |
rs554061613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616595 | GTCTTATCCCCCCGC[C/T]CCGCTTTTCCAAAGC | 84940 |
rs554126502 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624456 | GGTGATGCACACCTG[C/T]AATCCCAGCTACTCA | 84940 |
rs554390826 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623648 | TGGGCCTTGTTTGAA[C/T]TGGCGCCCGACTGTG | 84940 |
rs554413056 | snp | A/C | 0.067446 | 0.170804 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619233 | GTGGAATGAGGAGCC[A/C]CCCTGTCCCTCCACT | 84940 |
rs554496908 | snp | A/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622248 | CTTCTAGGGGTGGGG[A/T]CTTCAACCCCATCCT | 84940 |
rs554800825 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619355 | AAGCAGCTGGGAGCC[A/C]GGAGGGGGCACTGCC | 84940 |
rs555648198 | snp | G/T | 0.000559336 | 0.0167139 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617299 | ACTCGGCATCACCAG[G/T]TGGGGGCGCCAGCGC | 84940 |
rs556115783 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623522 | TGTAAAGTGAACCCA[C/T]CTTGACACTCCCTCC | 84940 |
rs556343915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616426 | TGGAGGCCAACACTT[A/G]CTCAGCGCCTACCAT | 84940 |
rs556436328 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621822 | ATGAGCATCTCTTCA[C/T]GGACGTGGTTGTAGC | 84940 |
rs556568259 | snp | C/T | 0.000114616 | 0.00756935 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616018 | TCCAGGATGTTGCGC[C/T]TCGTGACCCGGAGCT | 84940 |
rs558120106 | snp | A/C/G | 0.000554482 | 0.0166415 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617501 | TCCAGCTGCGTTACC[A/C/G]GGTCCCACAGGCCCA | 84940 |
rs558160459 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614307 | GTGCAAGCCCTGACT[C/T]CCTCATGGTGCCTCG | 84940 |
rs558775801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO6 | GRCh38.p7 | 17:29620924 | TGGAATCTGGCCAGG[C/T]TTGGCTGTGCTGTGT | 84940 |
rs558798899 | snp | A/C/T | 0.000112065 | 0.00748479 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615997 | GGGCCGGAGGGCGGG[A/C/T]GCACGTCCAGGATGT | 84940 |
rs558854907 | snp | C/T | 0.00988779 | 0.0696141 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622858 | CGATCCTGCGGCTCT[C/T]TAGAGCCCGGCGCCG | 84940 |
rs558961865 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615353 | CCCATCAAATCGCCA[C/T]CCGTTTGAGGTCAAG | 84940 |
rs559369269 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616944 | CGTGAGCACCTTGCC[A/G]CACAGGTAGACGATG | 84940 |
rs559432071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617790 | GGCCACGTCTGGCCC[C/T]TGACCTGGAGAGCAT | 84940 |
rs559510180 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624158 | TCTCTTTTACCTAAA[A/G]ATTCCAGGCACATGA | 84940 |
rs559552685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618650 | GTGGTTGCAGAGACG[C/G]GGGAAGGGGGCTAGT | 84940 |
rs559788502 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622275 | TCCTCCACCCCTGCC[A/C]CCGCCACGGCCAAGC | 84940 |
rs560291663 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615144 | GCAGCCCTCGCCCCT[A/G]TCGGTGGAAAGAAGG | 84940 |
rs560730542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617908 | TGTCTGCTGGCTCCC[C/T]GGAGTCGCAGCGAGG | 84940 |
rs560754662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | CORO6 | GRCh38.p7 | 17:29618544 | CCCAAAGCGAGGAGC[C/T]CTTCTCTGAGCTTCT | 84940 |
rs561730699 | snp | C/G | 1.759e-05 | 0.00296558 | intron-variant | CORO6 | GRCh38.p7 | 17:29616182 | GAGGTCTGACTGCGG[C/G]GGTGGGTGGACAGGA | 84940 |
rs561927325 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622609 | GCGGCGCGGGGGGAG[A/G]AGGCGCAGACCTCTG | 84940 |
rs562301918 | snp | G/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29616670 | GGGGGACAGAGGCGG[G/T]TAGGTGTTCAGGAGG | 84940 |
rs562749110 | snp | A/C | 1.67211e-05 | 0.00289142 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618832 | AATGATGCGCAAGGT[A/C]TTGTCCTTGCAGGTG | 84940 |
rs563169232 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615106 | TTCTCTCGAGATTTC[C/T]TCGCGGGGGCTGCCG | 84940 |
rs563541687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619337 | GGTGCATGCCTAGAA[C/T]AGAAGCAGCTGGGAG | 84940 |
rs563767409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620118 | TATTGAAGTGTCTGT[A/G]GGAATCTCCTGGTGG | 84940 |
rs563825608 | snp | A/T | 0.00163265 | 0.0285247 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622724 | GGCGCTCACGCTGCG[A/T]ATCCTCTGCGGAAGG | 84940 |
rs564109704 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622884 | CGCCGCTGCAGCCCC[A/C]GCTGCCGCTGCCATC | 84940 |
rs564508984 | snp | A/G | 1.70632e-05 | 0.00292084 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616147 | GGGCCTGGCGTATCC[A/G]GGTACAGATCGTCCT | 84940 |
rs565068730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619284 | AACCCTACTGGCTCT[C/T]TTGAGTGGTAAGGGT | 84940 |
rs565318023 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614943 | GGCTGGGGGTCTCGT[A/T]CCCCTCACTCCCACC | 84940 |
rs565349613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620512 | TTTCAGGCCTCTTCC[C/T]GACCCCGCCACCTGT | 84940 |
rs565723706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617441 | GGTGGGGGGCGCCTG[A/G]CCACTCTCCCGTGAT | 84940 |
rs565734749 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623076 | GCTGCTTCCCTCCCT[C/T]CATGACTCCCGGGTA | 84940 |
rs565737267 | snp | C/G | 0.000371264 | 0.0136196 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618094 | ATCCTGCTGAAGCCG[C/G]TGCTGAGCAGCTTCC | 84940 |
rs565883507 | snp | A/G | 3.97369e-05 | 0.00445723 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615960 | CGACAAGGGGGCGTC[A/G]CTGGCCGACTGGCTG | 84940 |
rs566102038 | snp | A/G | | | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621314 | GGCACAGAAGGAGCT[A/G]TCCCATGTGACCTTG | 84940 |
rs566123630 | snp | A/C/T | 0.000197845 | 0.00994412 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616784 | CTTTGCTGCTGAACG[A/C/T]GTTCAGGTAGTGCAC | 84940 |
rs566140873 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621666 | TGGCTAGGATTTGGG[A/G]CCTGAATTCTCCACA | 84940 |
rs566196337 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614279 | GAGTGTGTCCAACGT[A/G]GCCCCCTGGCCTGTG | 84940 |
rs566990899 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622640 | CCCCTCAGGGACCCC[G/T]CCCGCTCCGCTGGCT | 84940 |
rs567926594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619442 | CTGCTCTCCAGGCAC[C/T]AAGTTGGCCATGGCT | 84940 |
rs568108482 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624384 | GGAGTTCGAGACCAG[C/G]CTGGCCAACATGGCA | 84940 |
rs568118705 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO6 | GRCh38.p7 | 17:29616448 | GCCTACCATGCATAT[G/T]GCACATTACACACAT | 84940 |
rs568267864 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622519 | GCGAGACGAGGTGTC[G/T]GCGCCCTCCGGGAGC | 84940 |
rs568313195 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615247 | TGTGTCTGCAGAACT[G/T]GGGTGACGCCCATCT | 84940 |
rs568640924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620644 | TAAGGTTATGAAGCT[A/G]ACGTGGTAGTCATTG | 84940 |
rs569747580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29616396 | TTAACTTCTCCTGTC[G/T]AAGACCAAGGGGGTT | 84940 |
rs569893234 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619604 | AGGTGAGGCAGCCTT[C/G]CCTGCTCCCCTGCTC | 84940 |
rs570287288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618274 | GCACCCGCACCCCAG[A/G]TTAGACTTGAGGCTG | 84940 |
rs570341020 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622366 | ACACACTGAGCACTC[C/T]CAAAGCCCCAGCCAG | 84940 |
rs570345060 | in-del | -/CTTT | 0.00318978 | 0.0398085 | intron-variant | CORO6 | GRCh38.p7 | 17:29620729 | CTTCCTTTCCGTTCC[-/CTTT]CTTTCTACTTCACTG | 84940 |
rs570363958 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615208 | TAGCCACTGGGTCCG[G/T]CTCTGCAGCAAACGG | 84940 |
rs570426092 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614335 | TCGGAGAGTGGGGAG[C/T]ATATTGGGCTGGGGT | 84940 |
rs570749863 | snp | A/C | 0.00993419 | 0.0697739 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621791 | GCACCCCCCGCCCCC[A/C]CCACCGCCAGCCTTG | 84940 |
rs570958547 | snp | C/T | 0.000141288 | 0.00840381 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616001 | CGGAGGGCGGGCGCA[C/T]GTCCAGGATGTTGCG | 84940 |
rs571291653 | snp | A/G | 1.6703e-05 | 0.00288985 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619143 | TCAAGTGTGATGATA[A/G]GTTCCGTAATGTTGC | 84940 |
rs571811449 | snp | C/G/T | 0.000364646 | 0.0134979 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619653 | ACCTGGCTCCTACCA[C/G/T]GATGGTGGTGTCGTC | 84940 |
rs572258140 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615282 | TACCGCTCAGGGTGA[A/T]GGAATCCAGTGAGCT | 84940 |
rs572442949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO6 | GRCh38.p7 | 17:29616631 | ATTACTGGGGAAGCC[C/T]CGTGGCTAGGACCCG | 84940 |
rs572526415 | snp | G/T | | | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617327 | CGCAGGATCCTTCAC[G/T]CGACGCAGCAAAACT | 84940 |
rs572715312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619259 | CCACTCCTTCCCTAC[A/C]TTTTTTTTTAACCCT | 84940 |
rs573224495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29621150 | GAATGGAACTAGGTG[A/G]GAACAAAGGCTCAGG | 84940 |
rs573808512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617739 | AGCGGATGCGGGGAA[A/G]AGACAAATGGGGCCT | 84940 |
rs574484557 | snp | A/C/G | 5.93235e-05 | 0.00544599 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616049 | CGCGGTGCTTGGGGG[A/C/G]CACATAGCCGTCCCT | 84940 |
rs575105700 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615505 | CAGGCCTCCCTAGGC[C/G]AGCTCCAGCCGAGTC | 84940 |
rs575132754 | snp | A/T | 1.68224e-05 | 0.00290016 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619186 | AGTCTGGAATCTGCC[A/T]CACCTGGGTAGGAAG | 84940 |
rs575479156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | CORO6 | GRCh38.p7 | 17:29618514 | ATGGAGTTTCCAGCT[C/T]CTCCCCTCCTCAATC | 84940 |
rs576068352 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624007 | CTCAGGAAGAGTCCA[A/G]GTGGCTTGTAGGGAC | 84940 |
rs576247432 | snp | A/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624722 | GTAGTTGATGTAGCT[A/T]TGATTCTTACCCACG | 84940 |
rs576306381 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621823 | TGAGCATCTCTTCAC[A/G]GACGTGGTTGTAGCT | 84940 |
rs576517494 | snp | A/C | 1.64936e-05 | 0.00287168 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616764 | ACCCATGCCCCGCTG[A/C]GGCTCTTTGCTGCTG | 84940 |
rs576597497 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617575 | GCCCTGGCGCGTGAA[A/G]ACGGCCCGCATGGGC | 84940 |
rs576928992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29620000 | AGATGGCCTCATCAA[A/G]GACACACAACAAGAT | 84940 |
rs576979679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO6 | GRCh38.p7 | 17:29620929 | TCTGGCCAGGCTTGG[A/C]TGTGCTGTGTCCCAA | 84940 |
rs577117697 | snp | A/C/G | 0.000249314 | 0.0111622 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622739 | AATCCTCTGCGGAAG[A/C/G]GGCCCGAGTGCGTAG | 84940 |
rs577126644 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614998 | CTTAGTAAAATATTT[C/T]ATTCAGTACGTCTTG | 84940 |
rs577508607 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622072 | CTTGTGGGGGGACGG[A/G]TGGCAGCACAGAGTG | 84940 |
rs577590299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618405 | CCAGCCCTCGAGCCA[A/G]TGTCAGGCCCCAGAC | 84940 |
rs577793082 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624590 | CTCAAATAAAACACA[C/G]GCACAAAAAACCAAA | 84940 |
rs578059790 | snp | G/T | | | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615793 | GTGATGCGCTGCTCC[G/T]GGGCCTGCACCCGCT | 84940 |
rs578090794 | in-del | -/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621525 | GGTGGCTGATGAGAA[-/G]GGTTATGTGGTCAGG | 84940 |
rs745356686 | snp | C/T | 8.13129e-05 | 0.00637572 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621415 | GCCGAACCACACGTC[C/T]GCTCATAGCTGCAGG | 84940 |
rs745449634 | snp | A/G | 3.14976e-05 | 0.00396835 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617605 | CCTCATCCCCTCGTG[A/G]GCCGCAAACCTCTCC | 84940 |
rs745449873 | snp | A/C/T | 5.7046e-05 | 0.00534044 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617534 | TCTCGCTGGCTCATG[A/C/T]GGGTGAAGCCCGTGG | 84940 |
rs745534832 | snp | A/G | 5.29311e-05 | 0.00514419 | intron-variant | CORO6 | GRCh38.p7 | 17:29616184 | GGTCTGACTGCGGGG[A/G]TGGGTGGACAGGAGG | 84940 |
rs745762920 | snp | A/C | 1.67742e-05 | 0.002896 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621343 | TGGACACACGGATGT[A/C]CTCGTAGGCCTGGTC | 84940 |
rs745872126 | in-del | -/TT | 0.000126526 | 0.0079528 | intron-variant | CORO6 | GRCh38.p7 | 17:29616380 | CAGACTTCCACGTCC[-/TT]TTAACTTCTCCTGTC | 84940 |
rs745920369 | snp | A/C | 4.78457e-05 | 0.00489087 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617567 | AAGATATGGCCCTGG[A/C]GCGTGAAGACGGCCC | 84940 |
rs746007452 | snp | C/G | | | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618835 | GATGCGCAAGGTCTT[C/G]TCCTTGCAGGTGGTG | 84940 |
rs746020297 | snp | A/T | 1.66045e-05 | 0.00288132 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618959 | TTCCAGATGATGATC[A/T]CATTGTCACCACCTG | 84940 |
rs746114557 | snp | A/T | 1.69137e-05 | 0.00290802 | intron-variant | CORO6 | GRCh38.p7 | 17:29616672 | GGGACAGAGGCGGGT[A/T]GGTGTTCAGGAGGGG | 84940 |
rs746196281 | snp | C/G | 1.65625e-05 | 0.00287766 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619705 | GTCATTGTGTGGACA[C/G]CAGTCAATATCCAGC | 84940 |
rs746282111 | snp | A/T | 3.29766e-05 | 0.00406045 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617011 | TTGCTTGTGTCCATC[A/T]CCTGCAGTGCCACTG | 84940 |
rs746309758 | snp | A/T | 1.69295e-05 | 0.00290937 | intron-variant | CORO6 | GRCh38.p7 | 17:29621197 | AGCTAGTGTCCTCCC[A/T]CTTGCTTCCTTTCCC | 84940 |
rs746326129 | snp | C/T | 1.66034e-05 | 0.00288122 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617086 | CCTGCCCCACCCTCC[C/T]GTGCTACTTCGGGAC | 84940 |
rs746402340 | snp | C/G | 0.000653034 | 0.018058 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615945 | CAGGGCCGATCTTAC[C/G]GACAAGGGGGCGTCG | 84940 |
rs746578793 | snp | A/G | 2.48099e-05 | 0.00352198 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621410 | GCTTTGCCGAACCAC[A/G]CGTCTGCTCATAGCT | 84940 |
rs746591864 | snp | A/G | 1.67005e-05 | 0.00288963 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621337 | TGACCTTGGACACAC[A/G]GATGTCCTCGTAGGC | 84940 |
rs746595436 | snp | G/T | 3.11881e-05 | 0.00394881 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617384 | CAGGCGCTGCAGAGG[G/T]GGCAGCAGCCTTCAG | 84940 |
rs746634752 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624737 | ATGATTCTTACCCAC[A/G]TGGTCTGGCATCTGG | 84940 |
rs746683301 | snp | C/T | 2.09958e-05 | 0.00323998 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616041 | CCGGAGCTCGCGGTG[C/T]TTGGGGGGCACATAG | 84940 |
rs746683551 | snp | C/T | 3.64279e-05 | 0.00426762 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617525 | AGGCCCAGCTCTCGC[C/T]GGCTCATGCGGGTGA | 84940 |
rs746775422 | snp | C/T | 6.39673e-05 | 0.00565504 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622935 | GCATAGGGGCGGGGC[C/T]AGAGCCCAAGTTGCC | 84940 |
rs746798640 | snp | A/G | 5.22389e-05 | 0.00511045 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618791 | GGCCAGGCACTCACC[A/G]CCACCACTTGGCCTT | 84940 |
rs746834698 | in-del | -/G | 1.68519e-05 | 0.0029027 | intron-variant | CORO6 | GRCh38.p7 | 17:29616668 | GTGGGGGACAGAGGC[-/G]GGTAGGTGTTCAGGA | 84940 |
rs746844516 | snp | C/T | 1.66015e-05 | 0.00288105 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618954 | CCACATTCCAGATGA[C/T]GATCACATTGTCACC | 84940 |
rs746890219 | snp | C/T | 6.94887e-05 | 0.00589402 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616313 | ATGATAGGTTCACAC[C/T]TTCTTTCGTGTAGCT | 84940 |
rs746995426 | snp | A/C | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616751 | TTTTGGGCATGAAAC[A/C]CATGCCCCGCTGCGG | 84940 |
rs747079202 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620960 | CCATCTCCATCACCC[A/G]GCTCCCCTCCTGGTC | 84940 |
rs747097790 | snp | C/T | 1.70519e-05 | 0.00291987 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615808 | TGGGCCTGCACCCGC[C/T]CGCGGAGGGCCTTGA | 84940 |
rs747113285 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614489 | GACTGACTCTAAAAC[A/C]CTTCATCCAATGGTG | 84940 |
rs747131416 | snp | A/C | 3.31422e-05 | 0.00407063 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617080 | ACCAGCCCTGCCCCA[A/C]CCTCCCGTGCTACTT | 84940 |
rs747196619 | snp | G/T | 2.08474e-05 | 0.00322851 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622870 | TCTCTAGAGCCCGGC[G/T]CCGCTGCAGCCCCAG | 84940 |
rs747227902 | snp | C/G | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617748 | GGGGAAGAGACAAAT[C/G]GGGCCTAAGCACTCA | 84940 |
rs747290523 | in-del | -/AGACCAAGGGGGTTGGAGGCCAACA | 1.66646e-05 | 0.00288652 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619806 | AGATGTGGGGCTACT[-/AGACCAAGGGGGTTGGAGGCCAACA]CTCCTGTGTGTTTTT | 84940 |
rs747479235 | snp | C/G | 1.65636e-05 | 0.00287776 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619696 | GATAACGTTGTCATT[C/G]TGTGGACACCAGTCA | 84940 |
rs747534844 | snp | A/C | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616955 | TGCCACACAGGTAGA[A/C]GATGCTGGAGTCGGG | 84940 |
rs747653144 | snp | A/G/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624833 | GTGCTGAGCTAAAAC[A/G/T]TAACTGAGAGTTTAT | 84940 |
rs747764203 | snp | C/T | 1.66654e-05 | 0.00288659 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621241 | TGGCCAGAGGCAGGA[C/T]GATGAAGGCACCCCC | 84940 |
rs747839405 | in-del | -/G | 1.67097e-05 | 0.00289043 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619822 | TCCTGTGTGTTTTTT[-/G]GGGGAGTGGGTAGCA | 84940 |
rs747968836 | snp | A/G | 3.73385e-05 | 0.00432063 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618758 | GGCCACTGGTCAAGG[A/G]GTTCTGGGGAGTGGC | 84940 |
rs748107280 | snp | A/G | 2.0995e-05 | 0.00323991 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616292 | ACCTTGCGGGGCACA[A/G]TCATGATGATAGGTT | 84940 |
rs748179989 | in-del | -/TGCCCGAGCACAGGAGGCGTGACCAGCCCTGCCCCACCCTCCCG | 1.65132e-05 | 0.00287339 | splice-acceptor-variant, intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617043 | TCCTCGAAGTTGTTC[lengthTooLong]TGCCCGAGCACAGGA | 84940 |
rs748209061 | snp | C/T | 5.07679e-05 | 0.00503799 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619208 | GGTAGGAAGAAAAGG[C/T]ATATGGTGGGTGGAA | 84940 |
rs748262739 | snp | A/C | 0.000140984 | 0.00839477 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615723 | GCTCCGCCTGCCTGG[A/C]GCGCGGGGCTAGTCC | 84940 |
rs748435441 | snp | C/G | 3.39092e-05 | 0.00411746 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615798 | GCGCTGCTCCTGGGC[C/G]TGCACCCGCTCGCGG | 84940 |
rs748473267 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29621070 | TGGGGTGGCCTCCCC[C/T]CTGGTCCTTGAGGGC | 84940 |
rs748646132 | snp | A/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621936 | ACCACAGGATACCGA[A/T]CTCGCATCTCTGGAA | 84940 |
rs748839216 | snp | C/G | 2.0405e-05 | 0.00319407 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616279 | CTCCCGGCCCCTCAC[C/G]TTGCGGGGCACAGTC | 84940 |
rs748865676 | snp | A/T | 1.88414e-05 | 0.00306926 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618752 | ACAGCTGGCCACTGG[A/T]CAAGGGGTTCTGGGG | 84940 |
rs748866821 | snp | G/T | 1.81803e-05 | 0.00301494 | intron-variant | CORO6 | GRCh38.p7 | 17:29616199 | GTGGGTGGACAGGAG[G/T]ACTTGCGTGAGAGGG | 84940 |
rs749090830 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618682 | TCTGGAGCAGGGATG[C/T]GACAGGTGAAAGCCG | 84940 |
rs749138496 | snp | A/G | 4.68702e-05 | 0.00484076 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CORO6 | GRCh38.p7 | 17:29621449 | AGAGGTAGGATCTCA[A/G]TGCCCAGAAATGCCT | 84940 |
rs749156472 | snp | A/C | 0.000267881 | 0.0115702 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622733 | GCTGCGAATCCTCTG[A/C]GGAAGGGGCCCGAGT | 84940 |
rs749191368 | in-del | -/GG | 0.000108419 | 0.0073619 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622754 | GGGCCCGAGTGCGTA[-/GG]GGGCCGAGGAAGGCT | 84940 |
rs749244425 | snp | A/C | 3.47409e-05 | 0.00416764 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617617 | GTGGGCCGCAAACCT[A/C]TCCTGGGGGGAGGGG | 84940 |
rs749426935 | snp | C/G | 1.83155e-05 | 0.00302612 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617450 | CGCCTGGCCACTCTC[C/G]CGTGATGCCAGTCCC | 84940 |
rs749458210 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616774 | CGCTGCGGCTCTTTG[C/T]TGCTGAACGTGTTCA | 84940 |
rs749643271 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622110 | TCCCTCTTCTCCCAC[C/T]CCTTTCTGCACTGGC | 84940 |
rs749649305 | snp | A/C | 1.6664e-05 | 0.00288647 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621335 | TGTGACCTTGGACAC[A/C]CGGATGTCCTCGTAG | 84940 |
rs749731161 | snp | C/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624207 | AGTGACTCAGTTGCT[C/T]CTTTACAACAATAAC | 84940 |
rs749741100 | snp | A/C | 5.75424e-05 | 0.00536357 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617362 | AGAGGGGTGGGTGTG[A/C]GAATGGCAGGCGCTG | 84940 |
rs749748380 | snp | A/C | 2.62526e-05 | 0.00362293 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616025 | TGTTGCGCTTCGTGA[A/C]CCGGAGCTCGCGGTG | 84940 |
rs749792929 | snp | A/G | 1.78144e-05 | 0.00298444 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616074 | GTCCCTCAGCGAAAT[A/G]AGCACGGGTTCGGCG | 84940 |
rs749955218 | snp | C/T | 1.77697e-05 | 0.0029807 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615768 | CTCGCACAGCATGTT[C/T]TCCAGAGCCGTGATG | 84940 |
rs749985856 | snp | A/G | 3.29957e-05 | 0.00406162 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617023 | ATCTCCTGCAGTGCC[A/G]CTGGCTCCTCGAAGT | 84940 |
rs750089262 | snp | C/T | 5.57398e-05 | 0.0052789 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615843 | TTCCAGCAGCGTCTC[C/T]AGGGTGTGCTGCTGC | 84940 |
rs750117989 | snp | C/T | 0.000744879 | 0.0192843 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618129 | TGCGGTGAAGACAGC[C/T]CGCAGCGGGCGGGCG | 84940 |
rs750282704 | snp | G/T | 1.67483e-05 | 0.00289377 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619166 | AATGTTGCGCATGGG[G/T]GTATAGTCTGGAATC | 84940 |
rs750370647 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616836 | CTCAAAGTACCGAAT[A/G]CTGCTGTCGCCCTGC | 84940 |
rs750556654 | in-del | -/G | 1.67322e-05 | 0.00289237 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619163 | CGTAATGTTGCGCAT[-/G]GGGGTATAGTCTGGA | 84940 |
rs750651459 | snp | A/C/G/T | 5.11771e-05 | 0.00505832 | synonymous-codon, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616140 | CGGCTCCGGGCCTGG[A/C/G/T]GTATCCGGGTACAGA | 84940 |
rs750665921 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621687 | ATTCTCCACAGAGAC[A/C]CAGGCTGAGGGGATT | 84940 |
rs750836319 | snp | C/T | 1.65999e-05 | 0.00288091 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621316 | CACAGAAGGAGCTGT[C/T]CCATGTGACCTTGGA | 84940 |
rs750837268 | snp | A/T | 6.61288e-05 | 0.00574979 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616715 | ACCGGGCGATCTCAC[A/T]CTTGCTGACATCCAG | 84940 |
rs750922193 | snp | A/G | 3.53089e-05 | 0.00420157 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617307 | TCACCAGGTGGGGGC[A/G]CCAGCGCAGGATCCT | 84940 |
rs750964417 | snp | C/T | 3.53376e-05 | 0.00420328 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621371 | GTCGGCCTTTGCTGC[C/T]TGCCCAAACACATGG | 84940 |
rs751078194 | snp | C/T | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616811 | GCACGAAAGGCGGCT[C/T]GTCGGTAATCTCAAA | 84940 |
rs751180601 | snp | A/G | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618000 | GAAGGCGCTCCCGGC[A/G]GACCCAGAGAAGGAG | 84940 |
rs751216436 | snp | C/G | 1.64931e-05 | 0.00287163 | intron-variant | CORO6 | GRCh38.p7 | 17:29616899 | AGGCCCTCCACATCT[C/G]CATCCAGTGCCCTGT | 84940 |
rs751234960 | snp | A/G | 0.00013395 | 0.00818271 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615763 | ACCAGCTCGCACAGC[A/G]TGTTCTCCAGAGCCG | 84940 |
rs751245002 | snp | C/T | 0.000200622 | 0.0100135 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622713 | GCGGGCTGCGGGGCG[C/T]TCACGCTGCGAATCC | 84940 |
rs751302131 | snp | C/G | 1.84391e-05 | 0.00303632 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616061 | GGGGCACATAGCCGT[C/G]CCTCAGCGAAATGAG | 84940 |
rs751455587 | snp | C/T | 1.66757e-05 | 0.00288749 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619052 | GGACCCCTCCTTAGC[C/T]CCCAGACCTGCACTG | 84940 |
rs751573890 | snp | C/T | 5.01718e-05 | 0.00500833 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619158 | GGTTCCGTAATGTTG[C/T]GCATGGGGGTATAGT | 84940 |
rs751701245 | snp | G/T | 1.65899e-05 | 0.00288005 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621292 | TGGCCAGGAATTTGG[G/T]GTTGACGGCACAGAA | 84940 |
rs751764222 | snp | A/T | 1.83055e-05 | 0.00302529 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617291 | CCCCAGGGACTCGGC[A/T]TCACCAGGTGGGGGC | 84940 |
rs751956122 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614944 | GCTGGGGGTCTCGTT[C/T]CCCTCACTCCCACCC | 84940 |
rs752002811 | snp | C/G | 9.87281e-05 | 0.00702526 | intron-variant | CORO6 | GRCh38.p7 | 17:29616357 | AGGGAGCAGGGTTCA[C/G]CACCCTCGCAGACTT | 84940 |
rs752025357 | snp | A/G | 3.45018e-05 | 0.00415328 | intron-variant | CORO6 | GRCh38.p7 | 17:29621174 | GCTCAGGAGTTCCCA[A/G]GGGCCCCAGCTAGTG | 84940 |
rs752191034 | snp | C/G | 1.66757e-05 | 0.00288749 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619037 | CCACCCATCTATGGG[C/G]GACCCCTCCTTAGCC | 84940 |
rs752349475 | snp | A/T | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616795 | AACGTGTTCAGGTAG[A/T]GCACGAAAGGCGGCT | 84940 |
rs752483490 | snp | G/T | 7.80884e-05 | 0.00624805 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615917 | GGGAGATGTAGATTG[G/T]GCCAGAGTGCAGCAG | 84940 |
rs752584099 | snp | A/G | 0.000133932 | 0.00818217 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617264 | GCGCCGCATGCAGTC[A/G]CAGCAAACCACCCCC | 84940 |
rs752616932 | snp | A/G | 6.3014e-05 | 0.00561275 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622930 | GGCTAGCATAGGGGC[A/G]GGGCCAGAGCCCAAG | 84940 |
rs752675732 | snp | A/G | 3.89902e-05 | 0.00441515 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615990 | GCGGCGGGGGCCGGA[A/G]GGCGGGCGCACGTCC | 84940 |
rs752699569 | snp | C/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620147 | GGAAGAGGTCAAGGT[C/G]AGATAATAGTGTAGT | 84940 |
rs752797705 | snp | C/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623866 | AGTTATTACTTCCCA[C/T]CCTCCAGGGCACACC | 84940 |
rs752856330 | snp | C/T | 1.66012e-05 | 0.00288103 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619769 | TTCTTATCCACTCGC[C/T]CTGTCTGAGGGGTTG | 84940 |
rs753039230 | snp | C/G | 1.81352e-05 | 0.00301119 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622801 | CACCTCTCCGGGTGT[C/G]TGTAGTATCTGGGAC | 84940 |
rs753097679 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29616900 | GGCCCTCCACATCTC[C/T]ATCCAGTGCCCTGTT | 84940 |
rs753151189 | snp | C/T | 2.72031e-05 | 0.00368793 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617584 | CGTGAAGACGGCCCG[C/T]ATGGGCCTCATCCCC | 84940 |
rs753259381 | snp | C/T | 1.9691e-05 | 0.0031377 | intron-variant | CORO6 | GRCh38.p7 | 17:29616241 | CTCCGCTCCCTTCCG[C/T]CTCGTAGCCCTGCCC | 84940 |
rs753325023 | snp | C/G | 1.92432e-05 | 0.00310181 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622838 | GTCCAGCTCCGCACT[C/G]TGGCCGATCCTGCGG | 84940 |
rs753356165 | snp | C/G | 6.12351e-05 | 0.00553297 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622925 | GGCGGGGCTAGCATA[C/G]GGGCGGGGCCAGAGC | 84940 |
rs753435134 | snp | C/T | 6.63768e-05 | 0.00576056 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618909 | CGTCTGGGTGCATAT[C/T]ATCCAGGCTCAGCAG | 84940 |
rs753521016 | snp | A/C | 1.66663e-05 | 0.00288667 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619017 | GGTCCCACCTTTGCC[A/C]CCACCCACCCATCTA | 84940 |
rs753561854 | snp | A/G | 4.03088e-05 | 0.00448918 | intron-variant | CORO6 | GRCh38.p7 | 17:29616375 | CCCTCGCAGACTTCC[A/G]CGTCCTTAACTTCTC | 84940 |
rs753620095 | snp | C/T | 3.29766e-05 | 0.00406045 | intron-variant | CORO6 | GRCh38.p7 | 17:29616925 | CCTGTTCTCCCTGCC[C/T]GGCCGTGAGCACCTT | 84940 |
rs753645723 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620312 | GTCTTCACAGGCTGC[C/T]TGTGGGGGTTCTGAG | 84940 |
rs753662812 | snp | C/T | 0.000248812 | 0.011151 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619762 | TGGGTAGTTCTTATC[C/T]ACTCGCCCTGTCTGA | 84940 |
rs753712051 | snp | A/C | 1.65679e-05 | 0.00287814 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619745 | GTGTGCCCAGTGACC[A/C]GTGGGTAGTTCTTAT | 84940 |
rs753753114 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621497 | GAGCTGCGGGAGGGA[C/G]GAGGAGTGGAGGGGT | 84940 |
rs753816432 | snp | C/G | 0.000122572 | 0.00782756 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615777 | CATGTTCTCCAGAGC[C/G]GTGATGCGCTGCTCC | 84940 |
rs754029706 | snp | A/G | 1.65696e-05 | 0.00287828 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619666 | CATGATGGTGGTGTC[A/G]TCTGAGGCACTGGCG | 84940 |
rs754150094 | in-del | -/GAT | 0.000149381 | 0.00864108 | cds-indel, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618949 | GGTGCCCACATTCCA[-/GAT]GATGATCACATTGTC | 84940 |
rs754324519 | snp | A/C | 2.06571e-05 | 0.00321374 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621392 | AAACACATGGCGGAA[A/C]TTGCTTTGCCGAACC | 84940 |
rs754358584 | snp | A/C | | | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615936 | AGAGTGCAGCAGGGC[A/C]GATCTTACCGACAAG | 84940 |
rs754419520 | in-del | -/G | 1.75342e-05 | 0.00296087 | intron-variant | CORO6 | GRCh38.p7 | 17:29616180 | AAGAGGTCTGACTGC[-/G]GGGGTGGGTGGACAG | 84940 |
rs754428832 | snp | C/G/T | 7.9609e-05 | 0.00630866 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617582 | CGCGTGAAGACGGCC[C/G/T]GCATGGGCCTCATCC | 84940 |
rs754474252 | snp | A/C | 1.88191e-05 | 0.00306744 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618753 | CAGCTGGCCACTGGT[A/C]AAGGGGTTCTGGGGA | 84940 |
rs754492733 | snp | C/T | 1.65943e-05 | 0.00288043 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618912 | CTGGGTGCATATCAT[C/T]CAGGCTCAGCAGCAC | 84940 |
rs754498959 | snp | G/T | 9.38424e-05 | 0.00684926 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622928 | GGGGCTAGCATAGGG[G/T]CGGGGCCAGAGCCCA | 84940 |
rs754579051 | snp | C/T | 4.04179e-05 | 0.00449526 | intron-variant | CORO6 | GRCh38.p7 | 17:29616376 | CCTCGCAGACTTCCA[C/T]GTCCTTAACTTCTCC | 84940 |
rs754744978 | snp | A/C | 1.65356e-05 | 0.00287533 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617061 | CCCGAGCACAGGAGG[A/C]GTGACCAGCCCTGCC | 84940 |
rs754799036 | snp | A/G | 4.94654e-05 | 0.00497295 | intron-variant | CORO6 | GRCh38.p7 | 17:29616926 | CTGTTCTCCCTGCCC[A/G]GCCGTGAGCACCTTG | 84940 |
rs754914490 | snp | A/C | 1.9204e-05 | 0.00309865 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622842 | AGCTCCGCACTCTGG[A/C]CGATCCTGCGGCTCT | 84940 |
rs755007953 | snp | A/C | | | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617210 | TCTCCTCCTCCCCTG[A/C]GCACATAGCTCCTCC | 84940 |
rs755040488 | snp | G/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623507 | AAGGGGAGGACCGAG[G/T]GTAAAGTGAACCCAC | 84940 |
rs755044549 | snp | C/T | 1.68386e-05 | 0.00290155 | splice-acceptor-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619191 | GGAATCTGCCACACC[C/T]GGGTAGGAAGAAAAG | 84940 |
rs755146724 | in-del | -/TGCTCAGCG | 1.66713e-05 | 0.0028871 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619808 | ATGTGGGGCTACTCT[-/TGCTCAGCG]CCTGTGTGTTTTTTG | 84940 |
rs755199216 | snp | C/T | | | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621354 | ATGTCCTCGTAGGCC[C/T]GGTCGGCCTTTGCTG | 84940 |
rs755280721 | snp | C/G | 1.65652e-05 | 0.0028779 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619678 | GTCGTCTGAGGCACT[C/G]GCGATAACGTTGTCA | 84940 |
rs755398712 | snp | A/C | 1.79316e-05 | 0.00299424 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617514 | CCGGGTCCCACAGGC[A/C]CAGCTCTCGCTGGCT | 84940 |
rs755400712 | snp | G/T | 0.000303905 | 0.0123232 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622700 | TACCTGGTCCTGAGC[G/T]GGCTGCGGGGCGCTC | 84940 |
rs755607659 | snp | A/C/G | 0.000413328 | 0.0143709 | upstream-variant-2KB, utr-variant-5-prime, missense, stop-gained, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622730 | CACGCTGCGAATCCT[A/C/G]TGCGGAAGGGGCCCG | 84940 |
rs755623889 | snp | A/C | 3.77181e-05 | 0.00434253 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622829 | GACCCGGGTGTCCAG[A/C]TCCGCACTCTGGCCG | 84940 |
rs755650930 | snp | A/C/G | 0.000270256 | 0.0116216 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617609 | ATCCCCTCGTGGGCC[A/C/G]CAAACCTCTCCTGGG | 84940 |
rs755658116 | snp | A/G | 0.000126064 | 0.00793826 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615773 | ACAGCATGTTCTCCA[A/G]AGCCGTGATGCGCTG | 84940 |
rs755670079 | snp | A/T | 1.88777e-05 | 0.00307221 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618749 | CTGACAGCTGGCCAC[A/T]GGTCAAGGGGTTCTG | 84940 |
rs755810931 | snp | C/G | | | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617374 | GTGAGAATGGCAGGC[C/G]CTGCAGAGGTGGCAG | 84940 |
rs755964265 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618658 | AGAGACGGGGGAAGG[C/G]GGCTAGTCTCTGGAG | 84940 |
rs755981438 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616839 | AAAGTACCGAATGCT[C/G]CTGTCGCCCTGCAAA | 84940 |
rs756058918 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620168 | ATAGTGTAGTGCTGG[A/G]CAGCCCTTTCCTGGC | 84940 |
rs756130666 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621534 | TGAGAAGGGTTATGT[A/G]GTCAGGAGTCAGGTA | 84940 |
rs756147390 | snp | A/G | 1.78538e-05 | 0.00298774 | synonymous-codon, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617511 | TTACCGGGTCCCACA[A/G]GCCCAGCTCTCGCTG | 84940 |
rs756218114 | snp | C/T | 3.0232e-05 | 0.00388781 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616015 | ACGTCCAGGATGTTG[C/T]GCTTCGTGACCCGGA | 84940 |
rs756429595 | in-del | -/G | 3.30131e-05 | 0.00406269 | frameshift-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616044 | GAGCTCGCGGTGCTT[-/G]GGGGGCACATAGCCG | 84940 |
rs756441853 | snp | C/T | 1.65307e-05 | 0.0028749 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616716 | CCGGGCGATCTCACA[C/T]TTGCTGACATCCAGT | 84940 |
rs756579729 | snp | C/T | 1.66164e-05 | 0.00288235 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621325 | AGCTGTCCCATGTGA[C/T]CTTGGACACACGGAT | 84940 |
rs756618062 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618783 | AGTGGCCAGGCCAGG[C/T]ACTCACCGCCACCAC | 84940 |
rs756695203 | snp | G/T | 0.000196522 | 0.00991071 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617313 | GGTGGGGGCGCCAGC[G/T]CAGGATCCTTCACGC | 84940 |
rs756728914 | snp | C/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623885 | CCAGGGCACACCTGG[C/G]AGTGAGTGAATGGAA | 84940 |
rs756756692 | snp | A/G | 3.29788e-05 | 0.00406058 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616818 | AGGCGGCTCGTCGGT[A/G]ATCTCAAAGTACCGA | 84940 |
rs756950260 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615205 | GTGTAGCCACTGGGT[C/T]CGGCTCTGCAGCAAA | 84940 |
rs757092830 | snp | C/T | 3.29984e-05 | 0.00406179 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616754 | TGGGCATGAAACCCA[C/T]GCCCCGCTGCGGCTC | 84940 |
rs757122528 | snp | A/C/T | 3.3339e-05 | 0.00408272 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619053 | GACCCCTCCTTAGCC[A/C/T]CCAGACCTGCACTGA | 84940 |
rs757198283 | in-del | -/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620300 | ATCTATTTTTTGGTC[-/T]TCACAGGCTGCTTGT | 84940 |
rs757279068 | snp | C/T | 0.000199074 | 0.00997484 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621298 | GGAATTTGGGGTTGA[C/T]GGCACAGAAGGAGCT | 84940 |
rs757320168 | snp | C/T | 1.6569e-05 | 0.00287824 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617081 | CCAGCCCTGCCCCAC[C/T]CTCCCGTGCTACTTC | 84940 |
rs757464048 | snp | A/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618709 | GCCGGGACCAGGGGC[A/T]CTGATAATGGTGGGT | 84940 |
rs757527797 | snp | C/T | 2.02112e-05 | 0.00317887 | intron-variant | CORO6 | GRCh38.p7 | 17:29616271 | CAACCCTTCTCCCGG[C/T]CCCTCACCTTGCGGG | 84940 |
rs757640008 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624231 | CAATAACCCATGCTT[A/G]TGTGCTAGGCACTGG | 84940 |
rs757691636 | in-del | -/CA | 1.64855e-05 | 0.00287097 | frameshift-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616288 | CCTCACCTTGCGGGG[-/CA]CAGTCATGATGATAG | 84940 |
rs757790205 | in-del | -/G | 1.66599e-05 | 0.00288611 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619014 | CTGGGTCCCACCTTT[-/G]CCACCACCCACCCAT | 84940 |
rs757831068 | snp | G/T | 0.000395736 | 0.014061 | intron-variant | CORO6 | GRCh38.p7 | 17:29621177 | CAGGAGTTCCCAGGG[G/T]CCCCAGCTAGTGTCC | 84940 |
rs757918949 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619049 | GGGGGACCCCTCCTT[A/G]GCCCCCAGACCTGCA | 84940 |
rs758158396 | snp | A/C | 0.000145338 | 0.00852338 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617271 | ATGCAGTCACAGCAA[A/C]CCACCCCCAGGGACT | 84940 |
rs758165124 | snp | A/C/T | 3.33947e-05 | 0.00408613 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621336 | GTGACCTTGGACACA[A/C/T]GGATGTCCTCGTAGG | 84940 |
rs758180579 | snp | G/T | 3.99034e-05 | 0.00446656 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615925 | TAGATTGGGCCAGAG[G/T]GCAGCAGGGCCGATC | 84940 |
rs758183844 | snp | A/G | 0.000540833 | 0.0164354 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615992 | GGCGGGGGCCGGAGG[A/G]CGGGCGCACGTCCAG | 84940 |
rs758318761 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618934 | CAGCAGCACCTCCCC[A/G]GTGCCCACATTCCAG | 84940 |
rs758461627 | snp | A/G | 1.65638e-05 | 0.00287778 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619687 | GGCACTGGCGATAAC[A/G]TTGTCATTGTGTGGA | 84940 |
rs758479690 | snp | C/T | 3.29685e-05 | 0.00405995 | synonymous-codon, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616947 | GAGCACCTTGCCACA[C/T]AGGTAGACGATGCTG | 84940 |
rs758504557 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620637 | AGGGGCTTAAGGTTA[C/T]GAAGCTAACGTGGTA | 84940 |
rs758515367 | in-del | -/G | 1.67322e-05 | 0.00289237 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619162 | CGTAATGTTGCGCAT[-/G]GGGGGTATAGTCTGG | 84940 |
rs758660541 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621718 | GTGGAGCCTAACAGA[C/T]TGAAAGCTTTCTGGA | 84940 |
rs758684863 | snp | C/G | 5.55494e-05 | 0.00526988 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617589 | AGACGGCCCGCATGG[C/G]CCTCATCCCCTCGTG | 84940 |
rs758712172 | in-del | -/CTC | 4.39126e-05 | 0.00468555 | intron-variant | CORO6 | GRCh38.p7 | 17:29616388 | CCACGTCCTTAACTT[-/CTC]CTGTCTAAGACCAAG | 84940 |
rs758803022 | snp | C/T | 0.000508001 | 0.0159293 | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618116 | GCAGCTTCCCGTCTG[C/T]GGTGAAGACAGCCCG | 84940 |
rs758932234 | snp | C/T | 1.96821e-05 | 0.00313699 | intron-variant | CORO6 | GRCh38.p7 | 17:29616242 | TCCGCTCCCTTCCGC[C/T]TCGTAGCCCTGCCCA | 84940 |
rs758945705 | snp | A/G | 1.83122e-05 | 0.00302585 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617452 | CCTGGCCACTCTCCC[A/G]TGATGCCAGTCCCCG | 84940 |
rs759095626 | snp | A/G | 0.000201935 | 0.0100462 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615987 | GCTGCGGCGGGGGCC[A/G]GAGGGCGGGCGCACG | 84940 |
rs759141013 | snp | A/G | 1.66774e-05 | 0.00288763 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619034 | CACCCACCCATCTAT[A/G]GGGGACCCCTCCTTA | 84940 |
rs759167952 | in-del | -/G | 1.69169e-05 | 0.00290829 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618811 | CACTTGGCCTTTTCT[-/G]GGGTCAATGATGCGC | 84940 |
rs759211260 | snp | A/G | 1.66211e-05 | 0.00288275 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621257 | GATGAAGGCACCCCC[A/G]CCTCCAGCCTCCACA | 84940 |
rs759214286 | in-del | -/TTC | | | cds-indel, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615167 | AAAGAAGGAAGAGAG[-/TTC]TCTACCACAGACCGC | 84940 |
rs759251621 | in-del | -/T | 0.00576364 | 0.0533723 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622913 | CAACCTAAGAGGGCG[-/T]GGGCTAGCATAGGGG | 84940 |
rs759391584 | snp | C/G | 1.66316e-05 | 0.00288367 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621253 | GGACGATGAAGGCAC[C/G]CCCGCCTCCAGCCTC | 84940 |
rs759626347 | snp | C/G | 0.000341297 | 0.0130588 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622890 | TGCAGCCCCAGCTGC[C/G]GCTGCCATCAACCTA | 84940 |
rs759718653 | snp | A/C | 1.96632e-05 | 0.00313547 | intron-variant | CORO6 | GRCh38.p7 | 17:29616239 | TGCTCCGCTCCCTTC[A/C]GCCTCGTAGCCCTGC | 84940 |
rs759763909 | snp | C/T | 2.42639e-05 | 0.00348301 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616320 | GTTCACACTTTCTTT[C/T]GTGTAGCTTGTAGAA | 84940 |
rs759903357 | snp | A/C | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615024 | TCTTGTTTTTCTGAG[A/C]GAGGCAACGGCAGAG | 84940 |
rs759908976 | snp | A/G | 0.000107026 | 0.00731448 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622784 | CTTCAGGGCGAAGGA[A/G]CCACCTCTCCGGGTG | 84940 |
rs759922330 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant | CORO6 | GRCh38.p7 | 17:29616891 | CCCGGACAAGGCCCT[C/T]CACATCTCCATCCAG | 84940 |
rs759975194 | snp | A/C/T | 1.69045e-05 | 0.00290723 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615814 | TGCACCCGCTCGCGG[A/C/T]GGGCCTTGATCTCTT | 84940 |
rs759983378 | snp | C/G | | | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616756 | GGCATGAAACCCATG[C/G]CCCGCTGCGGCTCTT | 84940 |
rs760076776 | snp | G/T | 1.6649e-05 | 0.00288518 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621249 | GGCAGGACGATGAAG[G/T]CACCCCCGCCTCCAG | 84940 |
rs760231069 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CORO6 | GRCh38.p7 | 17:29621460 | CTCAGTGCCCAGAAA[C/T]GCCTTTGGTCCTTAG | 84940 |
rs760235550 | snp | C/G | 0.000115633 | 0.00760283 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617049 | GAAGTTGTTCTGCCC[C/G]AGCACAGGAGGCGTG | 84940 |
rs760321320 | snp | A/C | 0.000109499 | 0.00739848 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617235 | TCCTCCTCCCCTGCA[A/C]ATATACCCGCTGCGC | 84940 |
rs760321729 | snp | A/C | 7.35051e-05 | 0.00606194 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615880 | GGAGGACAGAGAGGC[A/C]GTGTCGTATAGGGGC | 84940 |
rs760339822 | snp | C/T | 0.00054439 | 0.0164894 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615976 | CTGGCCGACTGGCTG[C/T]GGCGGGGGCCGGAGG | 84940 |
rs760367073 | snp | C/T | 1.88873e-05 | 0.003073 | intron-variant | CORO6 | GRCh38.p7 | 17:29616215 | ACTTGCGTGAGAGGG[C/T]GCGGGGCTTGCTCCG | 84940 |
rs760371377 | snp | C/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622916 | ACCTAAGAGGGCGGG[C/G]CTAGCATAGGGGCGG | 84940 |
rs760386783 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619170 | TTGCGCATGGGGGTA[C/T]AGTCTGGAATCTGCC | 84940 |
rs760494066 | in-del | -/GCTGCGGGGCGCTCAC | 1.80029e-05 | 0.00300019 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622702 | CCTGGTCCTGAGCGG[-/GCTGCGGGGCGCTCAC]GCTGCGAATCCTCTG | 84940 |
rs760613230 | snp | C/T | 1.65658e-05 | 0.00287795 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619735 | CACAGGGGCAGTGTG[C/T]CCAGTGACCAGTGGG | 84940 |
rs760768811 | snp | A/G | 4.35246e-05 | 0.00466481 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617645 | GGGGAGACAGGGAGG[A/G]ACATCACCCAGCTGC | 84940 |
rs760834371 | snp | A/C | 0.00129842 | 0.0254465 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622688 | TGGGGGGCTGGGTAC[A/C]TGGTCCTGAGCGGGC | 84940 |
rs761021544 | snp | C/G/T | 6.59667e-05 | 0.00574279 | intron-variant | CORO6 | GRCh38.p7 | 17:29616916 | ATCCAGTGCCCTGTT[C/G/T]TCCCTGCCCGGCCGT | 84940 |
rs761284520 | snp | A/G | 1.64931e-05 | 0.00287163 | intron-variant | CORO6 | GRCh38.p7 | 17:29616901 | GCCCTCCACATCTCC[A/G]TCCAGTGCCCTGTTC | 84940 |
rs761374794 | snp | C/G | 1.65806e-05 | 0.00287924 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619651 | CCACCTGGCTCCTAC[C/G]ATGATGGTGGTGTCG | 84940 |
rs761465111 | snp | A/G | 1.65633e-05 | 0.00287774 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619719 | ACCAGTCAATATCCA[A/G]CACAGGGGCAGTGTG | 84940 |
rs761490098 | snp | C/T | 1.65045e-05 | 0.00287263 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617030 | GCAGTGCCACTGGCT[C/T]CTCGAAGTTGTTCTG | 84940 |
rs761673821 | snp | A/G | 1.86705e-05 | 0.0030553 | intron-variant | CORO6 | GRCh38.p7 | 17:29616212 | AGGACTTGCGTGAGA[A/G]GGTGCGGGGCTTGCT | 84940 |
rs761893368 | snp | A/G | 0.000756144 | 0.0194294 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622669 | CTGCGGTGACGGCCG[A/G]GTGTGGGGGGCTGGG | 84940 |
rs762162880 | snp | C/T | 1.66048e-05 | 0.00288134 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618894 | ACACACTGTGGATGA[C/T]GTCTGGGTGCATATC | 84940 |
rs762182866 | snp | C/T | 3.33278e-05 | 0.00408201 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619009 | GTCACCTGGGTCCCA[C/T]CTTTGCCACCACCCA | 84940 |
rs762189593 | snp | A/C | 3.31384e-05 | 0.00407039 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616706 | AGGCTGCTGACCGGG[A/C]GATCTCACACTTGCT | 84940 |
rs762272850 | snp | C/G | 1.6659e-05 | 0.00288604 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619091 | ATTCCTGGCAGTAGG[C/G]TGCCAGGAGAGGATG | 84940 |
rs762379931 | snp | C/T | 1.67122e-05 | 0.00289064 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619148 | TGTGATGATAGGTTC[C/T]GTAATGTTGCGCATG | 84940 |
rs762399585 | in-del | -/CTC | 8.67115e-05 | 0.00658394 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617196 | CCCCTGGGCACATCT[-/CTC]CTCCTCCCCTGCGCA | 84940 |
rs762471661 | snp | A/T | 3.29766e-05 | 0.00406045 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616803 | CAGGTAGTGCACGAA[A/T]GGCGGCTCGTCGGTA | 84940 |
rs762561774 | snp | C/T | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617924 | GGAGTCGCAGCGAGG[C/T]TTTTCCCGAATGGGA | 84940 |
rs762622246 | snp | C/T | 1.66582e-05 | 0.00288597 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619609 | AGGCAGCCTTCCCTG[C/T]TCCCCTGCTCAACTG | 84940 |
rs762705288 | snp | G/T | 1.70153e-05 | 0.00291674 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621351 | CGGATGTCCTCGTAG[G/T]CCTGGTCGGCCTTTG | 84940 |
rs762721743 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623206 | GGTGCCTCCACCCGC[A/G]TTCCAGCCTCAATCG | 84940 |
rs762806280 | snp | A/G | 4.13976e-05 | 0.0045494 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617551 | GGTGAAGCCCGTGGT[A/G]AAGATATGGCCCTGG | 84940 |
rs762817200 | snp | A/G | 1.70764e-05 | 0.00292197 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616121 | ATTCGTCCGCTTCTA[A/G]GGCCGGCTCCGGGCC | 84940 |
rs762879906 | snp | A/G | 1.86322e-05 | 0.00305217 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616059 | GGGGGGCACATAGCC[A/G]TCCCTCAGCGAAATG | 84940 |
rs762940025 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614759 | AAGAGGCTTCATACC[A/G]GAGGCTTTTGCTACC | 84940 |
rs763063962 | snp | C/T | 0.000166453 | 0.00912134 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618992 | CAGAGTGGCCAGGCA[C/T]GGTCACCTGGGTCCC | 84940 |
rs763101202 | snp | A/G | 5.58628e-05 | 0.00528472 | intron-variant | CORO6 | GRCh38.p7 | 17:29616339 | TAGCTTGTAGAACCT[A/G]TAAGGGAGCAGGGTT | 84940 |
rs763109169 | snp | C/T | 1.65968e-05 | 0.00288065 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621271 | CGCCTCCAGCCTCCA[C/T]AATAATGGCCAGGAA | 84940 |
rs763189102 | snp | C/T | 6.72009e-05 | 0.0057962 | intron-variant | CORO6 | GRCh38.p7 | 17:29616678 | GAGGCGGGTAGGTGT[C/T]CAGGAGGGGCCAAGG | 84940 |
rs763297725 | snp | A/G | 4.03983e-05 | 0.00449417 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615951 | CGATCTTACCGACAA[A/G]GGGGCGTCGCTGGCC | 84940 |
rs763325218 | snp | C/T | 6.64695e-05 | 0.00576457 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618873 | GGCTACCGTTGCTGT[C/T]CCAGCACACACTGTG | 84940 |
rs763359207 | snp | C/G | 0.00140911 | 0.026506 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615822 | CTCGCGGAGGGCCTT[C/G]ATCTCTTCCAGCAGC | 84940 |
rs763367696 | snp | C/T | 0.000122617 | 0.007829 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622810 | GGGTGTCTGTAGTAT[C/T]TGGGACCCGGGTGTC | 84940 |
rs763535509 | snp | C/T | 1.66297e-05 | 0.0028835 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619626 | CCCCTGCTCAACTGC[C/T]CAGCAGTAGCCACCT | 84940 |
rs763588603 | snp | A/G | 1.67125e-05 | 0.00289067 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619149 | GTGATGATAGGTTCC[A/G]TAATGTTGCGCATGG | 84940 |
rs763682305 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616807 | TAGTGCACGAAAGGC[A/G]GCTCGTCGGTAATCT | 84940 |
rs763690204 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | CORO6 | GRCh38.p7 | 17:29616895 | GACAAGGCCCTCCAC[A/G]TCTCCATCCAGTGCC | 84940 |
rs763815512 | snp | A/G | 1.81246e-05 | 0.00301031 | intron-variant, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617481 | CGAGGCACACACCCC[A/G]AGCCTCCAGCTGCGT | 84940 |
rs763823503 | snp | C/T | 1.85276e-05 | 0.00304359 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616060 | GGGGGCACATAGCCG[C/T]CCCTCAGCGAAATGA | 84940 |
rs763889716 | snp | A/G | 3.70295e-05 | 0.00430272 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615996 | GGGGCCGGAGGGCGG[A/G]CGCACGTCCAGGATG | 84940 |
rs764025870 | snp | A/G | 1.67531e-05 | 0.00289418 | intron-variant | CORO6 | GRCh38.p7 | 17:29616682 | CGGGTAGGTGTTCAG[A/G]AGGGGCCAAGGCTGC | 84940 |
rs764065500 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620267 | TGCCTACTATCCCCA[A/G]ATGGGAGCTGGGGGC | 84940 |
rs764274309 | snp | A/G | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621291 | ATGGCCAGGAATTTG[A/G]GGTTGACGGCACAGA | 84940 |
rs764300010 | snp | A/C | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617883 | CAAAGGCCGATCCCT[A/C]GAGCAGGGGTGTCTG | 84940 |
rs764336747 | in-del | -/T | 1.79851e-05 | 0.00299871 | frameshift-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616069 | AGCCGTCCCTCAGCG[-/T]AAATGAGCACGGGTT | 84940 |
rs764366051 | snp | C/T | 1.70156e-05 | 0.00291677 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621352 | GGATGTCCTCGTAGG[C/T]CTGGTCGGCCTTTGC | 84940 |
rs764366111 | snp | A/G | 1.89385e-05 | 0.00307716 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617281 | AGCAAACCACCCCCA[A/G]GGACTCGGCATCACC | 84940 |
rs764538701 | snp | A/C/G | 4.98536e-05 | 0.00499247 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618874 | GCTACCGTTGCTGTT[A/C/G]CAGCACACACTGTGG | 84940 |
rs764577758 | in-del | -/C | 1.6607e-05 | 0.00288153 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618883 | CTGTTCCAGCACACA[-/C]CTGTGGATGACGTCT | 84940 |
rs764867863 | snp | C/G | 1.67086e-05 | 0.00289033 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619144 | CAAGTGTGATGATAG[C/G]TTCCGTAATGTTGCG | 84940 |
rs764921678 | snp | A/G | 3.33522e-05 | 0.0040835 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619036 | CCCACCCATCTATGG[A/G]GGACCCCTCCTTAGC | 84940 |
rs764936433 | snp | C/T | 3.30267e-05 | 0.00406353 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616727 | CACACTTGCTGACAT[C/T]CAGTCCCCTTTTGGG | 84940 |
rs764942619 | snp | C/T | 3.32436e-05 | 0.00407685 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621256 | CGATGAAGGCACCCC[C/T]GCCTCCAGCCTCCAC | 84940 |
rs764962142 | snp | A/T | 0.000127771 | 0.00799182 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617262 | GCGCGCCGCATGCAG[A/T]CACAGCAAACCACCC | 84940 |
rs765017979 | snp | A/G/T | 9.92087e-05 | 0.00704241 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617062 | CCGAGCACAGGAGGC[A/G/T]TGACCAGCCCTGCCC | 84940 |
rs765103521 | snp | C/T | 6.2901e-05 | 0.00560772 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622929 | GGGCTAGCATAGGGG[C/T]GGGGCCAGAGCCCAA | 84940 |
rs765127813 | snp | A/G | 4.05145e-05 | 0.00450063 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615989 | TGCGGCGGGGGCCGG[A/G]GGGCGGGCGCACGTC | 84940 |
rs765206512 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614319 | ACTCCCTCATGGTGC[C/G]TCGGAGAGTGGGGAG | 84940 |
rs765349848 | snp | A/G | 3.93414e-05 | 0.00443499 | intron-variant | CORO6 | GRCh38.p7 | 17:29616240 | GCTCCGCTCCCTTCC[A/G]CCTCGTAGCCCTGCC | 84940 |
rs765437209 | snp | C/G | 2.46012e-05 | 0.00350713 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616321 | TTCACACTTTCTTTC[C/G]TGTAGCTTGTAGAAC | 84940 |
rs765504035 | snp | A/G | 4.97929e-05 | 0.00498939 | stop-gained, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619767 | AGTTCTTATCCACTC[A/G]CCCTGTCTGAGGGGT | 84940 |
rs765569712 | snp | A/G | 0.000137071 | 0.00827748 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615761 | CCACCAGCTCGCACA[A/G]CATGTTCTCCAGAGC | 84940 |
rs765608465 | in-del | -/CTT | 3.33511e-05 | 0.00408344 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619046 | TATGGGGGACCCCTC[-/CTT]AGCCCCCAGACCTGC | 84940 |
rs765750279 | snp | G/T | 0.000230388 | 0.0107304 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622796 | GGAGCCACCTCTCCG[G/T]GTGTCTGTAGTATCT | 84940 |
rs765815355 | snp | C/G | 2.68944e-05 | 0.00366694 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617583 | GCGTGAAGACGGCCC[C/G]CATGGGCCTCATCCC | 84940 |
rs765910666 | snp | C/G | 0.000601142 | 0.0173266 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618012 | GGCAGACCCAGAGAA[C/G]GAGCGAGCTAGCGCG | 84940 |
rs765931087 | snp | A/G | 2.11222e-05 | 0.00324972 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617244 | CCTGCACATATACCC[A/G]CTGCGCGCCGCATGC | 84940 |
rs765986880 | snp | A/G | 0.000244768 | 0.01106 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622924 | GGGCGGGGCTAGCAT[A/G]GGGGCGGGGCCAGAG | 84940 |
rs766020064 | snp | A/G | 1.68869e-05 | 0.00290571 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615982 | GACTGGCTGCGGCGG[A/G]GGCCGGAGGGCGGGC | 84940 |
rs766023143 | snp | C/G | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617977 | CTTGGGCGCCAGCCA[C/G]AGCCCGGGAAGGCGC | 84940 |
rs766050251 | in-del | -/G | 3.60399e-05 | 0.00424484 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617622 | CCGCAAACCTCTCCT[-/G]GGGGGAGGGGGAGAC | 84940 |
rs766081044 | snp | A/G | 1.65949e-05 | 0.00288048 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618905 | ATGACGTCTGGGTGC[A/G]TATCATCCAGGCTCA | 84940 |
rs766158357 | snp | A/G | 1.65737e-05 | 0.00287864 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619661 | CCTACCATGATGGTG[A/G]TGTCGTCTGAGGCAC | 84940 |
rs766304604 | snp | C/T | 2.63703e-05 | 0.00363104 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617580 | GGCGCGTGAAGACGG[C/T]CCGCATGGGCCTCAT | 84940 |
rs766473849 | in-del | -/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624869 | GTGGCACAGAGGAAA[-/G]GATGCCTGGAATGAA | 84940 |
rs766492308 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617051 | AGTTGTTCTGCCCGA[A/G]CACAGGAGGCGTGAC | 84940 |
rs766521906 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623243 | CAATTTAGCTGTCCC[A/G]ATCGGCCGGGACTGC | 84940 |
rs766590347 | snp | C/T | 5.25804e-05 | 0.00512713 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617666 | ACCCAGCTGCCTGCC[C/T]TGAGGAGCATGGAGG | 84940 |
rs766672965 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616791 | GCTGAACGTGTTCAG[A/G]TAGTGCACGAAAGGC | 84940 |
rs767055302 | snp | A/T | 3.64325e-05 | 0.0042679 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622692 | GGGCTGGGTACCTGG[A/T]CCTGAGCGGGCTGCG | 84940 |
rs767075706 | snp | A/G | 3.29821e-05 | 0.00406078 | intron-variant | CORO6 | GRCh38.p7 | 17:29616906 | CCACATCTCCATCCA[A/G]TGCCCTGTTCTCCCT | 84940 |
rs767080785 | snp | G/T | 1.78083e-05 | 0.00298393 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615767 | GCTCGCACAGCATGT[G/T]CTCCAGAGCCGTGAT | 84940 |
rs767119846 | snp | A/G | 6.17113e-05 | 0.00555444 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615838 | ATCTCTTCCAGCAGC[A/G]TCTCCAGGGTGTGCT | 84940 |
rs767132185 | snp | A/G | 1.85211e-05 | 0.00304306 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622819 | TAGTATCTGGGACCC[A/G]GGTGTCCAGCTCCGC | 84940 |
rs767160000 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617033 | GTGCCACTGGCTCCT[C/T]GAAGTTGTTCTGCCC | 84940 |
rs767457231 | snp | C/T | 1.74196e-05 | 0.00295119 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621365 | GGCCTGGTCGGCCTT[C/T]GCTGCCTGCCCAAAC | 84940 |
rs767581329 | snp | C/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623738 | CAAGGAGATTAAAGA[C/T]AACCTGATCAAAATA | 84940 |
rs767712452 | snp | C/T | 3.89355e-05 | 0.00441206 | intron-variant | CORO6 | GRCh38.p7 | 17:29616373 | CACCCTCGCAGACTT[C/T]CACGTCCTTAACTTC | 84940 |
rs767713288 | in-del | -/CTTTA | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624208 | GTGACTCAGTTGCTC[-/CTTTA]CAACAATAACCCATG | 84940 |
rs767851479 | snp | A/G | 2.44484e-05 | 0.00349623 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617572 | ATGGCCCTGGCGCGT[A/G]AAGACGGCCCGCATG | 84940 |
rs767949789 | snp | C/T | 1.65356e-05 | 0.00287533 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616714 | GACCGGGCGATCTCA[C/T]ACTTGCTGACATCCA | 84940 |
rs767987373 | snp | A/G | 6.59794e-05 | 0.00574329 | intron-variant | CORO6 | GRCh38.p7 | 17:29616880 | TCAGGGGCGCGCCCG[A/G]ACAAGGCCCTCCACA | 84940 |
rs768074824 | snp | C/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624742 | TCTTACCCACGTGGT[C/G]TGGCATCTGGTTCTT | 84940 |
rs768144987 | snp | A/G | 1.83542e-05 | 0.00302932 | intron-variant | CORO6 | GRCh38.p7 | 17:29616204 | TGGACAGGAGGACTT[A/G]CGTGAGAGGGTGCGG | 84940 |
rs768147951 | snp | C/G | 0.000386175 | 0.0138902 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622693 | GGCTGGGTACCTGGT[C/G]CTGAGCGGGCTGCGG | 84940 |
rs768275465 | snp | C/T | 5.23327e-05 | 0.00511504 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CORO6 | GRCh38.p7 | 17:29621452 | GGTAGGATCTCAGTG[C/T]CCAGAAATGCCTTTG | 84940 |
rs768393522 | snp | A/C | 1.65633e-05 | 0.00287774 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619710 | TGTGTGGACACCAGT[A/C]AATATCCAGCACAGG | 84940 |
rs768452219 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623508 | AGGGGAGGACCGAGT[A/G]TAAAGTGAACCCACC | 84940 |
rs768467904 | snp | A/G | 2.23371e-05 | 0.00334187 | synonymous-codon, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617560 | CGTGGTGAAGATATG[A/G]CCCTGGCGCGTGAAG | 84940 |
rs768570038 | snp | G/T | 3.256e-05 | 0.00403472 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615685 | AAAAGCCGGGGCGGG[G/T]CCGAGCTTGTGCGCC | 84940 |
rs768617307 | in-del | -/AGTGCAC | 1.64885e-05 | 0.00287123 | frameshift-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616793 | TGAACGTGTTCAGGT[-/AGTGCAC]GAAAGGCGGCTCGTC | 84940 |
rs768623627 | snp | C/T | | | splice-acceptor-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617621 | GCCGCAAACCTCTCC[C/T]GGGGGGAGGGGGAGA | 84940 |
rs768726483 | snp | G/T | 8.32841e-05 | 0.00645253 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619087 | GGACATTCCTGGCAG[G/T]AGGGTGCCAGGAGAG | 84940 |
rs768812994 | snp | A/G/T | 3.29866e-05 | 0.00406108 | intron-variant | CORO6 | GRCh38.p7 | 17:29616871 | TCAGTCGGTTCAGGG[A/G/T]CGCGCCCGGACAAGG | 84940 |
rs768816410 | snp | C/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616775 | GCTGCGGCTCTTTGC[C/T]GCTGAACGTGTTCAG | 84940 |
rs768908886 | snp | G/T | 4.7995e-05 | 0.00489849 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616031 | GCTTCGTGACCCGGA[G/T]CTCGCGGTGCTTGGG | 84940 |
rs769109106 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29621005 | GGTGGTGCATGGAGA[A/G]GTGGGAGGGCTAGGG | 84940 |
rs769130089 | snp | C/G | 8.65763e-05 | 0.0065788 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617373 | TGTGAGAATGGCAGG[C/G]GCTGCAGAGGTGGCA | 84940 |
rs769184207 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619388 | CTCTCCAGAGACCTC[C/T]CATTCACTCCAGCAG | 84940 |
rs769188988 | snp | G/T | 1.7144e-05 | 0.00292775 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616110 | GCCGGATAGCCATTC[G/T]TCCGCTTCTAGGGCC | 84940 |
rs769435927 | snp | A/G | 1.78036e-05 | 0.00298353 | intron-variant | CORO6 | GRCh38.p7 | 17:29616188 | TGACTGCGGGGGTGG[A/G]TGGACAGGAGGACTT | 84940 |
rs769547833 | in-del | -/CCGAGCACAGGAGGCG | 1.66092e-05 | 0.00288172 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617090 | CCCACCCTCCCGTGC[-/CCGAGCACAGGAGGCG]TACTTCGGGACCCCC | 84940 |
rs769703221 | snp | A/G | 1.64947e-05 | 0.00287177 | stop-gained, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616763 | AACCCATGCCCCGCT[A/G]CGGCTCTTTGCTGCT | 84940 |
rs769758908 | snp | A/G | 8.17294e-05 | 0.00639203 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621416 | CCGAACCACACGTCT[A/G]CTCATAGCTGCAGGC | 84940 |
rs769810589 | snp | C/G | 1.83142e-05 | 0.00302601 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617459 | ACTCTCCCGTGATGC[C/G]AGTCCCCGAGGCACA | 84940 |
rs770055458 | snp | G/T | 1.65949e-05 | 0.00288048 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617087 | CTGCCCCACCCTCCC[G/T]TGCTACTTCGGGACC | 84940 |
rs770123429 | snp | A/C | 5.48501e-05 | 0.00523661 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616063 | GGCACATAGCCGTCC[A/C]TCAGCGAAATGAGCA | 84940 |
rs770187298 | snp | G/T | 0.00740318 | 0.0603886 | intron-variant | CORO6 | GRCh38.p7 | 17:29616675 | ACAGAGGCGGGTAGG[G/T]GTTCAGGAGGGGCCA | 84940 |
rs770214037 | snp | A/G | | | intron-variant | CORO6 | GRCh38.p7 | 17:29621164 | GAGAACAAAGGCTCA[A/G]GAGTTCCCAGGGGCC | 84940 |
rs770232965 | snp | C/T | 4.05293e-05 | 0.00450145 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615948 | GGCCGATCTTACCGA[C/T]AAGGGGGCGTCGCTG | 84940 |
rs770267301 | snp | A/C | 3.33812e-05 | 0.00408528 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621229 | GATCCCTCACCTTGG[A/C]CAGAGGCAGGACGAT | 84940 |
rs770268033 | snp | G/T | 0.000351247 | 0.0132476 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622891 | GCAGCCCCAGCTGCC[G/T]CTGCCATCAACCTAA | 84940 |
rs770292515 | snp | C/G | 1.66985e-05 | 0.00288946 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621338 | GACCTTGGACACACG[C/G]ATGTCCTCGTAGGCC | 84940 |
rs770301809 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621940 | CAGGATACCGAACTC[A/G]CATCTCTGGAATAGT | 84940 |
rs770478240 | in-del | -/GGGCGGGGCTAGCATAG | 0.338585 | 0.233779 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622909 | GCCATCAACCTAAGA[-/GGGCGGGGCTAGCATAG]GGGCGGGGCCAGAGC | 84940 |
rs770601736 | snp | A/C | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619532 | AGGAGCTGGGCAGGG[A/C]AGGGCCCTGGGACCC | 84940 |
rs770617846 | snp | C/T | 4.74372e-05 | 0.00486994 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616317 | TAGGTTCACACTTTC[C/T]TTCGTGTAGCTTGTA | 84940 |
rs770663335 | snp | C/G | 1.83775e-05 | 0.00303124 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617528 | CCCAGCTCTCGCTGG[C/G]TCATGCGGGTGAAGC | 84940 |
rs770717814 | snp | C/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614953 | CTCGTTCCCCTCACT[C/T]CCACCCATGCAGGAG | 84940 |
rs770755881 | snp | C/G | 8.10209e-05 | 0.00636426 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616045 | AGCTCGCGGTGCTTG[C/G]GGGGCACATAGCCGT | 84940 |
rs770835337 | snp | A/G | 8.30117e-05 | 0.00644197 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618955 | CACATTCCAGATGAT[A/G]ATCACATTGTCACCA | 84940 |
rs770854544 | snp | G/T | | | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616304 | ACAGTCATGATGATA[G/T]GTTCACACTTTCTTT | 84940 |
rs770971772 | snp | A/C | 0.00010044 | 0.0070859 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621251 | CAGGACGATGAAGGC[A/C]CCCCCGCCTCCAGCC | 84940 |
rs770991457 | snp | C/G | 9.79576e-05 | 0.0069978 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615810 | GGCCTGCACCCGCTC[C/G]CGGAGGGCCTTGATC | 84940 |
rs771160389 | snp | C/G | 0.00122081 | 0.0246762 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622871 | CTCTAGAGCCCGGCG[C/G]CGCTGCAGCCCCAGC | 84940 |
rs771226997 | snp | A/T | 6.62515e-05 | 0.00575512 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619697 | ATAACGTTGTCATTG[A/T]GTGGACACCAGTCAA | 84940 |
rs771314206 | snp | A/G | 1.64939e-05 | 0.0028717 | intron-variant | CORO6 | GRCh38.p7 | 17:29616883 | GGGGCGCGCCCGGAC[A/G]AGGCCCTCCACATCT | 84940 |
rs771317541 | snp | A/G | 1.68298e-05 | 0.00290079 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618818 | CCTTTTCTGGGGTCA[A/G]TGATGCGCAAGGTCT | 84940 |
rs771642925 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619727 | ATATCCAGCACAGGG[A/G]CAGTGTGCCCAGTGA | 84940 |
rs771711028 | snp | A/G | 3.91474e-05 | 0.00442404 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617629 | CCTCTCCTGGGGGGA[A/G]GGGGAGACAGGGAGG | 84940 |
rs771730733 | snp | A/G | 1.66563e-05 | 0.0028858 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621242 | GGCCAGAGGCAGGAC[A/G]ATGAAGGCACCCCCG | 84940 |
rs771832728 | snp | A/G/T | 1.65941e-05 | 0.00288041 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621308 | GTTGACGGCACAGAA[A/G/T]GAGCTGTCCCATGTG | 84940 |
rs771888486 | snp | A/G | 1.87051e-05 | 0.00305813 | intron-variant | CORO6 | GRCh38.p7 | 17:29616213 | GGACTTGCGTGAGAG[A/G]GTGCGGGGCTTGCTC | 84940 |
rs771896033 | snp | A/C | 9.37603e-05 | 0.00684626 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617204 | CACATCTCTCCTCCT[A/C]CCCTGCGCACATAGC | 84940 |
rs771920824 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622564 | GGCCAAATATAGACA[C/T]CACGTCCTCCCCGCC | 84940 |
rs771934319 | snp | C/T | 1.82493e-05 | 0.00302065 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618770 | AGGGGTTCTGGGGAG[C/T]GGCCAGGCCAGGCAC | 84940 |
rs772048161 | snp | C/G | 2.20194e-05 | 0.00331801 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616305 | CAGTCATGATGATAG[C/G]TTCACACTTTCTTTC | 84940 |
rs772136445 | snp | A/C | 0.000102182 | 0.00714705 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615803 | GCTCCTGGGCCTGCA[A/C]CCGCTCGCGGAGGGC | 84940 |
rs772198313 | snp | G/T | 0.000321492 | 0.0126745 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615724 | CTCCGCCTGCCTGGC[G/T]CGCGGGGCTAGTCCG | 84940 |
rs772560923 | snp | A/T | 1.72332e-05 | 0.00293535 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616102 | GCGTCCTGGCCGGAT[A/T]GCCATTCGTCCGCTT | 84940 |
rs772611039 | snp | C/T | 1.6943e-05 | 0.00291053 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619212 | GGAAGAAAAGGTATA[C/T]GGTGGGTGGAATGAG | 84940 |
rs772756514 | snp | A/G | 3.90648e-05 | 0.00441937 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615964 | AAGGGGGCGTCGCTG[A/G]CCGACTGGCTGCGGC | 84940 |
rs772790637 | in-del | -/GACCAGCCCTGCCCC | 1.66109e-05 | 0.00288187 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617091 | CCACCCTCCCGTGCT[-/GACCAGCCCTGCCCC]ACTTCGGGACCCCCA | 84940 |
rs772898226 | snp | A/G | 1.66535e-05 | 0.00288556 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621243 | GCCAGAGGCAGGACG[A/G]TGAAGGCACCCCCGC | 84940 |
rs772910964 | snp | C/T | 3.30382e-05 | 0.00406423 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617048 | CGAAGTTGTTCTGCC[C/T]GAGCACAGGAGGCGT | 84940 |
rs772940477 | snp | C/G | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617890 | CGATCCCTAGAGCAG[C/G]GGTGTCTGCTGGCTC | 84940 |
rs772981019 | in-del | -/T | 0.000110406 | 0.00742904 | upstream-variant-2KB, utr-variant-5-prime, frameshift-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622751 | AGGGGCCCGAGTGCG[-/T]TAGGGGGCCGAGGAA | 84940 |
rs772993131 | snp | A/G | 2.2848e-05 | 0.00337986 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616311 | TGATGATAGGTTCAC[A/G]CTTTCTTTCGTGTAG | 84940 |
rs772998862 | snp | A/G | 0.000107556 | 0.00733255 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617232 | AGCTCCTCCTCCCCT[A/G]CACATATACCCGCTG | 84940 |
rs773074195 | snp | A/C | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624879 | GGAAAGGATGCCTGG[A/C]ATGAATTAAAAAACT | 84940 |
rs773126156 | snp | C/T | 0.000181637 | 0.00952813 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615727 | CGCCTGCCTGGCGCG[C/T]GGGGCTAGTCCGTGC | 84940 |
rs773205661 | snp | G/T | 0.000602954 | 0.0173526 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622675 | TGACGGCCGGGTGTG[G/T]GGGGCTGGGTACCTG | 84940 |
rs773314445 | snp | A/G | 1.65649e-05 | 0.00287788 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619729 | ATCCAGCACAGGGGC[A/G]GTGTGCCCAGTGACC | 84940 |
rs773382960 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614715 | TCCCTGATGCCAGGG[C/G]CACCAGACTGATTCT | 84940 |
rs773488786 | snp | A/C | 4.26667e-05 | 0.00461861 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617642 | GAGGGGGAGACAGGG[A/C]GGGACATCACCCAGC | 84940 |
rs773559369 | snp | A/C/T | 0.000216738 | 0.0104082 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622752 | AGGGGCCCGAGTGCG[A/C/T]AGGGGGCCGAGGAAG | 84940 |
rs773724310 | snp | G/T | 1.6495e-05 | 0.0028718 | intron-variant | CORO6 | GRCh38.p7 | 17:29616875 | TCGGTTCAGGGGCGC[G/T]CCCGGACAAGGCCCT | 84940 |
rs773839176 | in-del | -/T | 0.00579705 | 0.053525 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622912 | TCAACCTAAGAGGGC[-/T]GGGGCTAGCATAGGG | 84940 |
rs773886858 | snp | C/T | 1.64996e-05 | 0.0028722 | synonymous-codon, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617025 | CTCCTGCAGTGCCAC[C/T]GGCTCCTCGAAGTTG | 84940 |
rs773918842 | in-del | -/TG | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614683 | AGAACAAAGAGAAAC[-/TG]TTCCTCCCACCCCCT | 84940 |
rs774034604 | in-del | -/CAT | 4.3957e-05 | 0.00468792 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617646 | GGAGACAGGGAGGGA[-/CAT]CATCACCCAGCTGCC | 84940 |
rs774053469 | snp | A/C | 1.66087e-05 | 0.00288168 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619637 | CTGCCCAGCAGTAGC[A/C]ACCTGGCTCCTACCA | 84940 |
rs774081532 | snp | A/G | 4.61926e-05 | 0.00480564 | stop-gained, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617565 | TGAAGATATGGCCCT[A/G]GCGCGTGAAGACGGC | 84940 |
rs774086397 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619916 | TAACCCCATCCAGTC[C/T]ACTTCCTGCACTTTA | 84940 |
rs774109811 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29618444 | ATGCGTCTGGGTGCC[A/G]GCTGAGAGGAGAGGG | 84940 |
rs774141399 | snp | C/T | 1.6563e-05 | 0.00287771 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619715 | GGACACCAGTCAATA[C/T]CCAGCACAGGGGCAG | 84940 |
rs774174366 | snp | C/T | 5.15858e-05 | 0.00507841 | intron-variant | CORO6 | GRCh38.p7 | 17:29621178 | AGGAGTTCCCAGGGG[C/T]CCCAGCTAGTGTCCT | 84940 |
rs774248959 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616778 | GCGGCTCTTTGCTGC[C/T]GAACGTGTTCAGGTA | 84940 |
rs774271748 | snp | C/T | 1.70676e-05 | 0.00292122 | missense, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616130 | CTTCTAGGGCCGGCT[C/T]CGGGCCTGGCGTATC | 84940 |
rs774290038 | snp | C/T | 1.8434e-05 | 0.0030359 | intron-variant | CORO6 | GRCh38.p7 | 17:29616205 | GGACAGGAGGACTTG[C/T]GTGAGAGGGTGCGGG | 84940 |
rs774422358 | snp | C/G | 1.71761e-05 | 0.00293049 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621358 | CCTCGTAGGCCTGGT[C/G]GGCCTTTGCTGCCTG | 84940 |
rs774467325 | snp | A/T | | | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617558 | CCCGTGGTGAAGATA[A/T]GGCCCTGGCGCGTGA | 84940 |
rs774635768 | snp | C/T | 1.99619e-05 | 0.0031592 | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622657 | CCGCTCCGCTGGCTG[C/T]GGTGACGGCCGGGTG | 84940 |
rs774728282 | snp | A/T | 1.66576e-05 | 0.00288592 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619088 | GACATTCCTGGCAGT[A/T]GGGTGCCAGGAGAGG | 84940 |
rs774773768 | snp | G/T | 2.44281e-05 | 0.00349477 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615717 | CGCCCCGCTCCGCCT[G/T]CCTGGCGCGCGGGGC | 84940 |
rs774818421 | snp | A/G | 2.20792e-05 | 0.00332252 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616037 | TGACCCGGAGCTCGC[A/G]GTGCTTGGGGGGCAC | 84940 |
rs774911504 | snp | G/T | 1.66554e-05 | 0.00288573 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619002 | AGGCATGGTCACCTG[G/T]GTCCCACCTTTGCCA | 84940 |
rs774930255 | snp | A/T | 1.66355e-05 | 0.002884 | intron-variant | CORO6 | GRCh38.p7 | 17:29616695 | AGGAGGGGCCAAGGC[A/T]GCTGACCGGGCGATC | 84940 |
rs775006298 | snp | C/T | 1.71973e-05 | 0.0029323 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619240 | GAGGAGCCACCCTGT[C/T]CCTCCACTCCTTCCC | 84940 |
rs775022235 | snp | C/G | 1.70942e-05 | 0.00292349 | missense, stop-lost, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616118 | GCCATTCGTCCGCTT[C/G]TAGGGCCGGCTCCGG | 84940 |
rs775284578 | snp | A/G | 1.82573e-05 | 0.00302131 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617467 | GTGATGCCAGTCCCC[A/G]AGGCACACACCCCAA | 84940 |
rs775301092 | snp | C/G | 1.87623e-05 | 0.00306281 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616058 | TGGGGGGCACATAGC[C/G]GTCCCTCAGCGAAAT | 84940 |
rs775308342 | snp | C/T | 1.68403e-05 | 0.0029017 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621348 | ACACGGATGTCCTCG[C/T]AGGCCTGGTCGGCCT | 84940 |
rs775400353 | snp | C/G | 3.39403e-05 | 0.00411934 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CORO6 | GRCh38.p7 | 17:29621431 | GCTCATAGCTGCAGG[C/G]AGAGAGGTAGGATCT | 84940 |
rs775414694 | snp | A/G | 2.00604e-05 | 0.00316698 | missense, utr-variant-5-prime, utr-variant-3-prime, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617546 | ATGCGGGTGAAGCCC[A/G]TGGTGAAGATATGGC | 84940 |
rs775436497 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621934 | CCACCACAGGATACC[A/G]AACTCGCATCTCTGG | 84940 |
rs775659192 | snp | A/G | 2.49299e-05 | 0.00353048 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616323 | CACACTTTCTTTCGT[A/G]TAGCTTGTAGAACCT | 84940 |
rs775673078 | snp | A/C | 8.1616e-05 | 0.00638759 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615819 | CCGCTCGCGGAGGGC[A/C]TTGATCTCTTCCAGC | 84940 |
rs775818856 | snp | G/T | 1.6821e-05 | 0.00290004 | intron-variant | CORO6 | GRCh38.p7 | 17:29616677 | AGAGGCGGGTAGGTG[G/T]TCAGGAGGGGCCAAG | 84940 |
rs775878877 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617089 | GCCCCACCCTCCCGT[A/G]CTACTTCGGGACCCC | 84940 |
rs775982453 | snp | G/T | 6.66345e-05 | 0.00577172 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619086 | AGGACATTCCTGGCA[G/T]TAGGGTGCCAGGAGA | 84940 |
rs776038423 | snp | A/C | 8.02729e-05 | 0.00633483 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615949 | GCCGATCTTACCGAC[A/C]AGGGGGCGTCGCTGG | 84940 |
rs776064973 | snp | A/G | 3.32519e-05 | 0.00407736 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618865 | GGCTAGCAGGCTACC[A/G]TTGCTGTTCCAGCAC | 84940 |
rs776096355 | snp | A/G | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29623737 | TCAAGGAGATTAAAG[A/G]TAACCTGATCAAAAT | 84940 |
rs776156815 | snp | A/C/T | 3.66495e-05 | 0.00428058 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617451 | GCCTGGCCACTCTCC[A/C/T]GTGATGCCAGTCCCC | 84940 |
rs776206130 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619984 | GTGACACAGAGAGGT[A/G]AGATGGCCTCATCAA | 84940 |
rs776233847 | snp | A/G | 3.98748e-05 | 0.00446495 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615984 | CTGGCTGCGGCGGGG[A/G]CCGGAGGGCGGGCGC | 84940 |
rs776247867 | snp | G/T | 0.0234296 | 0.105669 | intron-variant | CORO6 | GRCh38.p7 | 17:29616671 | GGGGACAGAGGCGGG[G/T]AGGTGTTCAGGAGGG | 84940 |
rs776274372 | in-del | -/ATGC | 3.29685e-05 | 0.00405995 | frameshift-variant, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616957 | CCACACAGGTAGACG[-/ATGC]TGGAGTCGGGATCGT | 84940 |
rs776422694 | snp | A/C | 8.32009e-05 | 0.0064493 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621252 | AGGACGATGAAGGCA[A/C]CCCCGCCTCCAGCCT | 84940 |
rs776439177 | snp | C/T | 2.10466e-05 | 0.0032439 | intron-variant, synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617245 | CTGCACATATACCCG[C/T]TGCGCGCCGCATGCA | 84940 |
rs776633059 | snp | A/G | 1.67377e-05 | 0.00289284 | synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621341 | CTTGGACACACGGAT[A/G]TCCTCGTAGGCCTGG | 84940 |
rs776901500 | snp | A/G | 5.72754e-05 | 0.00535111 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | CORO6 | GRCh38.p7 | 17:29617668 | CCAGCTGCCTGCCCT[A/G]AGGAGCATGGAGGGA | 84940 |
rs776924661 | snp | C/T | 4.83162e-05 | 0.00491485 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616319 | GGTTCACACTTTCTT[C/T]CGTGTAGCTTGTAGA | 84940 |
rs776931265 | snp | A/G | 6.59718e-05 | 0.00574296 | intron-variant | CORO6 | GRCh38.p7 | 17:29616886 | GCGCGCCCGGACAAG[A/G]CCCTCCACATCTCCA | 84940 |
rs777025921 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29614358 | GCTGGGGTAAGCACT[A/G]GACCCAAGTAGACTG | 84940 |
rs777071554 | in-del | -/AGCATAGGGGCGGGGCCAG | 0.00032803 | 0.0128026 | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29622919 | TAAGAGGGCGGGGCT[-/AGCATAGGGGCGGGGCCAG]AGCCCAAGTTGCCCC | 84940 |
rs777178326 | snp | C/G/T | 0.000182916 | 0.00956161 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615812 | CCTGCACCCGCTCGC[C/G/T]GAGGGCCTTGATCTC | 84940 |
rs777312313 | snp | A/G | 3.55809e-05 | 0.00421772 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622778 | GGAAGGCTTCAGGGC[A/G]AAGGAGCCACCTCTC | 84940 |
rs777387291 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29618676 | CTAGTCTCTGGAGCA[C/G]GGATGCGACAGGTGA | 84940 |
rs777497701 | snp | A/G | 4.62107e-05 | 0.00480658 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621403 | GGAACTTGCTTTGCC[A/G]AACCACACGTCTGCT | 84940 |
rs777582042 | snp | A/G | 3.26184e-05 | 0.00403834 | intron-variant, utr-variant-5-prime, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617380 | ATGGCAGGCGCTGCA[A/G]AGGTGGCAGCAGCCT | 84940 |
rs777628026 | snp | C/T | 1.6681e-05 | 0.00288794 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619051 | GGGACCCCTCCTTAG[C/T]CCCCAGACCTGCACT | 84940 |
rs777737033 | snp | C/T | 4.97855e-05 | 0.00498902 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618939 | GCACCTCCCCGGTGC[C/T]CACATTCCAGATGAT | 84940 |
rs777789069 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616952 | CCTTGCCACACAGGT[A/G]GACGATGCTGGAGTC | 84940 |
rs777922878 | snp | G/T | 4.0252e-05 | 0.00448602 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615929 | TTGGGCCAGAGTGCA[G/T]CAGGGCCGATCTTAC | 84940 |
rs777949067 | snp | C/T | 1.656e-05 | 0.00287745 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617073 | AGGCGTGACCAGCCC[C/T]GCCCCACCCTCCCGT | 84940 |
rs778034169 | snp | G/T | 0.000195886 | 0.00989469 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615806 | CCTGGGCCTGCACCC[G/T]CTCGCGGAGGGCCTT | 84940 |
rs778214886 | snp | G/T | 5.28267e-05 | 0.00513912 | intron-variant | CORO6 | GRCh38.p7 | 17:29616183 | AGGTCTGACTGCGGG[G/T]GTGGGTGGACAGGAG | 84940 |
rs778264119 | snp | A/C | 3.31268e-05 | 0.00406968 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619693 | GGCGATAACGTTGTC[A/C]TTGTGTGGACACCAG | 84940 |
rs778302525 | snp | A/T | 1.99679e-05 | 0.00315967 | intron-variant | CORO6 | GRCh38.p7 | 17:29616263 | GCCCTGCCCAACCCT[A/T]CTCCCGGCCCCTCAC | 84940 |
rs778327121 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29622019 | GTTCCTCCTGTCCAC[C/T]AATCTGAGTCCTTTC | 84940 |
rs778354451 | snp | C/T | 1.65965e-05 | 0.00288062 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618925 | ATCCAGGCTCAGCAG[C/T]ACCTCCCCGGTGCCC | 84940 |
rs778358180 | snp | C/T | 2.08967e-05 | 0.00323232 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616290 | TCACCTTGCGGGGCA[C/T]AGTCATGATGATAGG | 84940 |
rs778397406 | snp | A/G | | | utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant | CORO6, ANKRD13B | GRCh38.p7 | 17:29615248 | GTGTCTGCAGAACTG[A/G]GGTGACGCCCATCTG | 84940 |
rs778423366 | snp | A/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624143 | GGTATGTGAGTCATC[A/T]CTCTTTTACCTAAAG | 84940 |
rs778506223 | snp | C/T | 1.69571e-05 | 0.00291174 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615797 | TGCGCTGCTCCTGGG[C/T]CTGCACCCGCTCGCG | 84940 |
rs778715265 | snp | A/C | 1.66751e-05 | 0.00288744 | | | GRCh38.p7 | 17:29621236 | CACCTTGGCCAGAGG[A/C]AGGACGATGAAGGCA | 84940 |
rs778905256 | snp | A/G | 0.000859968 | 0.0207182 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622852 | TCTGGCCGATCCTGC[A/G]GCTCTCTAGAGCCCG | 84940 |
rs779002941 | snp | A/G | 1.68795e-05 | 0.00290507 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619197 | TGCCACACCTGGGTA[A/G]GAAGAAAAGGTATAT | 84940 |
rs779062013 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | CORO6 | GRCh38.p7 | 17:29616931 | CTCCCTGCCCGGCCG[C/T]GAGCACCTTGCCACA | 84940 |
rs779106213 | snp | A/G/T | 5.0314e-05 | 0.00501543 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618825 | TGGGGTCAATGATGC[A/G/T]CAAGGTCTTGTCCTT | 84940 |
rs779117454 | in-del | -/ATG | 6.34363e-05 | 0.00563153 | cds-indel, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616295 | TTGCGGGGCACAGTC[-/ATG]ATGATAGGTTCACAC | 84940 |
rs779122841 | snp | C/T | | | intron-variant | CORO6 | GRCh38.p7 | 17:29620425 | GGGGAGGAGGCAGCT[C/T]CGGCTGAAATTTGAG | 84940 |
rs779382095 | snp | G/T | 1.82317e-05 | 0.00301919 | synonymous-codon, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617523 | ACAGGCCCAGCTCTC[G/T]CTGGCTCATGCGGGT | 84940 |
rs779383257 | snp | C/G | | | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617156 | CTATGCCCCAAACCT[C/G]TAGTGACCAGAGTTG | 84940 |
rs779498612 | snp | A/G | 0.000138188 | 0.00831114 | upstream-variant-2KB, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622833 | CGGGTGTCCAGCTCC[A/G]CACTCTGGCCGATCC | 84940 |
rs779542111 | snp | C/T | 1.74078e-05 | 0.00295019 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616091 | GCACGGGTTCGGCGT[C/T]CTGGCCGGATAGCCA | 84940 |
rs779547196 | snp | A/G | 1.78973e-05 | 0.00299137 | intron-variant | CORO6 | GRCh38.p7 | 17:29616191 | CTGCGGGGGTGGGTG[A/G]ACAGGAGGACTTGCG | 84940 |
rs779580009 | snp | C/T | | | upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29624263 | ACTAAGGGCTTTATA[C/T]GTATTAATTTCATAC | 84940 |
rs779817411 | snp | A/G | 4.07639e-05 | 0.00451445 | splice-donor-variant | CORO6 | GRCh38.p7 | 17:29616277 | TTCTCCCGGCCCCTC[A/G]CCTTGCGGGGCACAG | 84940 |
rs779957773 | snp | A/C | 1.64923e-05 | 0.00287156 | intron-variant | CORO6 | GRCh38.p7 | 17:29616851 | GCTGCTGTCGCCCTG[A/C]AAAATCAGTCGGTTC | 84940 |
rs780116908 | snp | C/T | 1.78395e-05 | 0.00298654 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616073 | CGTCCCTCAGCGAAA[C/T]GAGCACGGGTTCGGC | 84940 |
rs780155786 | snp | A/G | 1.67542e-05 | 0.00289427 | missense, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619171 | TGCGCATGGGGGTAT[A/G]GTCTGGAATCTGCCA | 84940 |
rs780210955 | snp | A/C | 0.000123693 | 0.0078633 | missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29615776 | GCATGTTCTCCAGAG[A/C]CGTGATGCGCTGCTC | 84940 |
rs780256611 | in-del | -/AGA | 0.000332513 | 0.0128898 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619786 | TGTCTGAGGGGTTGG[-/AGA]AGAAGATGTGGGGCT | 84940 |
rs780377164 | in-del | -/GT | 1.67472e-05 | 0.00289367 | intron-variant | CORO6 | GRCh38.p7 | 17:29616653 | TAGGACCCGACATGA[-/GT]GGGGGACAGAGGCGG | 84940 |
rs780518511 | snp | C/T | 1.66244e-05 | 0.00288304 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29621327 | CTGTCCCATGTGACC[C/T]TGGACACACGGATGT | 84940 |
rs780672620 | snp | C/G/T | 3.5802e-05 | 0.00423084 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617513 | ACCGGGTCCCACAGG[C/G/T]CCAGCTCTCGCTGGC | 84940 |
rs780676189 | snp | A/T | 1.86876e-05 | 0.0030567 | missense, utr-variant-5-prime, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617531 | AGCTCTCGCTGGCTC[A/T]TGCGGGTGAAGCCCG | 84940 |
rs780862794 | snp | A/G | 0.00183262 | 0.0302151 | upstream-variant-2KB, utr-variant-5-prime, missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29622723 | GGGCGCTCACGCTGC[A/G]AATCCTCTGCGGAAG | 84940 |
rs781042452 | in-del | -/TG | 1.66807e-05 | 0.00288792 | intron-variant, upstream-variant-2KB | CORO6 | GRCh38.p7 | 17:29619811 | GTGGGGCTACTCTCC[-/TG]TGTGTTTTTTGGGGA | 84940 |
rs781163770 | snp | C/G/T | 3.2992e-05 | 0.00406142 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616757 | GCATGAAACCCATGC[C/G/T]CCGCTGCGGCTCTTT | 84940 |
rs781178718 | snp | C/T | 4.05014e-05 | 0.0044999 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29615942 | CAGCAGGGCCGATCT[C/T]ACCGACAAGGGGGCG | 84940 |
rs781273061 | snp | C/T | 0.000114607 | 0.00756903 | intron-variant, missense, downstream-variant-500B, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29617246 | TGCACATATACCCGC[C/T]GCGCGCCGCATGCAG | 84940 |
rs781340228 | snp | C/G | 1.64909e-05 | 0.00287144 | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616832 | TAATCTCAAAGTACC[C/G]AATGCTGCTGTCGCC | 84940 |
rs781552260 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO6 | GRCh38.p7 | 17:29621926 | GACTGCAGCCACCAC[A/G]GGATACCGAACTCGC | 84940 |
rs781567271 | snp | A/G | 1.65627e-05 | 0.00287769 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29619702 | GTTGTCATTGTGTGG[A/G]CACCAGTCAATATCC | 84940 |
rs781577273 | snp | A/C | 1.66056e-05 | 0.00288141 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29618958 | ATTCCAGATGATGAT[A/C]ACATTGTCACCACCT | 84940 |
rs781603158 | snp | C/T | 0.000447564 | 0.0149527 | intron-variant, downstream-variant-500B | CORO6 | GRCh38.p7 | 17:29617085 | CCCTGCCCCACCCTC[C/T]CGTGCTACTTCGGGA | 84940 |
rs796412073 | snp | C/T | | | missense, nc-transcript-variant | CORO6 | GRCh38.p7 | 17:29616302 | GCACAGTCATGATGA[C/T]AGGTTCACACTTTCT | 84940 |