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 |