SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs750133 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108667009 | AAATAGGCCACACTC[A/G]TGGCTTACTGTGCGG | 23603 |
rs750134 | snp | G/T | 0.184203 | 0.241186 | intron-variant | CORO1C | GRCh38.p7 | 12:108667330 | CTGATCTCTGTGCAG[G/T]CTTGTTAGCTTTTCT | 23603 |
rs750135 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | CORO1C | GRCh38.p7 | 12:108666963 | ACCCTTAACAAAACT[A/G]CCACTCTCTGAGCCT | 23603 |
rs961355 | snp | A/G | 0.488118 | 0.0761554 | intron-variant | CORO1C | GRCh38.p7 | 12:108672036 | GTGCCTCACACCTGT[A/G]ATTCCAGCAATTTGG | 23603 |
rs1060665 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645400 | TGATGGTGGTGAAAC[A/C]CCGTAGGGCATGTGG | 23603 |
rs1077167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658277 | gggtggatcatttga[A/G]gtcaggagtttgaga | 23603 |
rs1079088 | snp | A/C | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108667755 | AATGGGATTTTACTG[A/C]TGGATTCACTTTTTC | 23603 |
rs1344512 | snp | C/T | 0.436123 | 0.166908 | intron-variant | CORO1C | GRCh38.p7 | 12:108696263 | GGAGAAAGAAAGCAA[C/T]TTGGGAAGACAGGAG | 23603 |
rs1344513 | snp | G/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108696805 | TTACAAAAGAGAGTG[G/T]GAATCACGTGTGCTA | 23603 |
rs1345421 | snp | G/T | 0.394721 | 0.203852 | intron-variant | CORO1C | GRCh38.p7 | 12:108691259 | TGCCCTCTCAGCTCA[G/T]TCTTCCCCAGACTCA | 23603 |
rs1362614 | snp | C/T | 0.18989 | 0.242666 | intron-variant | CORO1C | GRCh38.p7 | 12:108670182 | GTGTTTGCTCCCACC[C/T]GCTTAAATTTTGGGG | 23603 |
rs1362615 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CORO1C | GRCh38.p7 | 12:108667072 | TTTTTTTTTTTGCCA[C/T]GCGCTATTCTAAGCC | 23603 |
rs1549088 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108723540 | ACTATGGTCTCTCAT[A/G]AAAAATCTACAGCTT | 23603 |
rs1861638 | snp | A/C | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108671681 | TAGGTGTTGCTGTCA[A/C]AGTCAGATTATAATC | 23603 |
rs1861639 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108668422 | TTTTTGCCCTGAAAT[A/G]AAAATGGAAGTGATG | 23603 |
rs1861640 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668378 | CAGGCATTCAGCAGG[C/G]AGGGCTTCGTCTTAA | 23603 |
rs1861641 | snp | A/G | 0.434976 | 0.168179 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658167 | GGGCGAAAAGCAACA[A/G]GTTCTCTCATCAGCT | 23603 |
rs2111211 | snp | A/G | 0.431916 | 0.171483 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646093 | AGCAGAAACAGGAGC[A/G]CAGACCTCTGCTGTA | 23603 |
rs2111212 | snp | G/T | 0.395087 | 0.203592 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646018 | CTGCCTCTCCATCTC[G/T]CACCAAGGCTGCGTC | 23603 |
rs2302700 | snp | A/G | 0.368529 | 0.220116 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731563 | GCCGCCACCGCCCCC[A/G]MCACCGCGCGTAGGC | 23603 |
rs2302701 | snp | A/C | 0.368529 | 0.220116 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731564 | CCGCCACCGCCCCCG[A/C]CACCGCGCGTAGGCC | 23603 |
rs3741782 | snp | C/T | 0.42798 | 0.175566 | intron-variant | CORO1C | GRCh38.p7 | 12:108701361 | AAGCTTTCAGTTTGG[C/T]GCATAATTCTAACAT | 23603 |
rs3782519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662648 | TTCTTGAGTGTTTCA[A/G]TCATTTTGTAGTTTT | 23603 |
rs3825252 | snp | G/T | 0.223225 | 0.248562 | intron-variant | CORO1C | GRCh38.p7 | 12:108715542 | GGGACCAAAAGAGGT[G/T]GTTGTGTTTATAAAG | 23603 |
rs3825253 | snp | C/T | 0.161924 | 0.233971 | intron-variant | CORO1C | GRCh38.p7 | 12:108715505 | GTGATAAGCAGAAAA[C/T]TGGGAGATGTGGAGG | 23603 |
rs3837483 | in-del | -/G | 0.175254 | 0.238565 | intron-variant | CORO1C | GRCh38.p7 | 12:108721990 | GCCTGCTTTAGAAAG[-/G]TTCTTCCTGTCACTC | 23603 |
rs3839976 | in-del | -/CACCTCCTTT | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108690286 | GGGTTTATTCCAGAG[-/CACCTCCTTT]TACCTCAAGGATGGT | 23603 |
rs4014703 | in-del | -/CCTGGA/CTGGAC | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703779 | GCCTGACTATGGGCC[-/CCTGGA/CTGGAC]TGGATGACACCCAGC | 23603 |
rs4964272 | snp | A/G | 0.43598 | 0.167067 | intron-variant | CORO1C | GRCh38.p7 | 12:108709839 | TTCAACTTTGGAAAA[A/G]CTGCTTGCTCATTAG | 23603 |
rs4964273 | snp | G/T | 0.447032 | 0.153878 | intron-variant | CORO1C | GRCh38.p7 | 12:108709897 | GCATAGGCTTTCCCT[G/T]GCTTGCAACAGTAAG | 23603 |
rs4964274 | snp | G/T | 0.367503 | 0.220665 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732212 | TACCACCACCTCCCT[G/T]GAGGACTGCCGACGT | 23603 |
rs4964731 | snp | A/C | 0.443732 | 0.158012 | intron-variant | CORO1C | GRCh38.p7 | 12:108664033 | AAACAAACAACCTCT[A/C]AGAAAAGGGCTGAGT | 23603 |
rs4964734 | snp | A/G | 0.394538 | 0.203982 | intron-variant | CORO1C | GRCh38.p7 | 12:108693760 | CTTCTTTGCCCTCCT[A/G]GGGACAGAGCCCCTC | 23603 |
rs4964736 | snp | C/T | 0.408017 | 0.193729 | intron-variant | CORO1C | GRCh38.p7 | 12:108706727 | agcctcccgagtagc[C/T]gggactacactgcac | 23603 |
rs4964737 | snp | A/C | 0.44252 | 0.159487 | intron-variant | CORO1C | GRCh38.p7 | 12:108706732 | cccgagtagccggga[A/C]tacactgcacccagc | 23603 |
rs5800834 | in-del | -/A | 0.401924 | 0.198543 | intron-variant | CORO1C | GRCh38.p7 | 12:108678719 | GATGTTCCATGGCTT[-/A]AAAAAAAAAAAAAAA | 23603 |
rs5800835 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | CORO1C | GRCh38.p7 | 12:108694793 | ATATTTCTACGTAGA[-/T]TTTTTTCTTAAAGGC | 23603 |
rs6539449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658109 | TTGTCAAGGTATGTG[A/G]TTTTGTTGAGGTCCA | 23603 |
rs6539450 | snp | G/T | 0.488666 | 0.0744214 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658554 | TAAAAGCTGGAAAAT[G/T]TACAACTCTGGAGAG | 23603 |
rs7135100 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | CORO1C | GRCh38.p7 | 12:108705691 | tacagaccaatatct[C/G]ttatgaatacagatg | 23603 |
rs7136703 | snp | A/C | 0.43978 | 0.162738 | intron-variant | CORO1C | GRCh38.p7 | 12:108728679 | CAGAAAGGAGTACAG[A/C]ATCTTGTTCACTCAC | 23603 |
rs7295054 | snp | A/T | 0.488394 | 0.0752869 | intron-variant | CORO1C | GRCh38.p7 | 12:108725825 | tttatttatttattt[A/T]tttgagacggattct | 23603 |
rs7296370 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | CORO1C | GRCh38.p7 | 12:108730007 | CAGGCAGAAAGGCTG[A/C]GGTAAGAGGGCCTAA | 23603 |
rs7298543 | snp | G/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733475 | ccactgtgcccACAA[G/T]TCAATAGTTTTGAAC | 23603 |
rs7300215 | snp | A/G | 0.403509 | 0.197319 | intron-variant | CORO1C | GRCh38.p7 | 12:108695618 | GGCAACATCTGAGCT[A/G]GATAATGAACAGGAA | 23603 |
rs7300726 | snp | C/T | 0.411242 | 0.191052 | intron-variant | CORO1C | GRCh38.p7 | 12:108660086 | GTGGATTCTTGCCAA[C/T]AAAGCAATTTGGAAA | 23603 |
rs7304904 | snp | G/T | 0.109108 | 0.206518 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731719 | CCGAGGGATGCAGGC[G/T]GTGCCCAAGCGCACG | 23603 |
rs7310556 | snp | C/G | 0.393987 | 0.204372 | intron-variant | CORO1C | GRCh38.p7 | 12:108655590 | tttcgctgtgttggc[C/G]gggctggtctccagc | 23603 |
rs7312102 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CORO1C | GRCh38.p7 | 12:108694776 | ATATGTATATAGATA[C/T]TATATTTCTACGTAG | 23603 |
rs7313667 | snp | G/T | 0.245346 | 0.249957 | intron-variant | CORO1C | GRCh38.p7 | 12:108698939 | ACTCATGAACCTATC[G/T]ACTATAGAAACCCAA | 23603 |
rs7313999 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656138 | gtgaggagcccctcc[A/G]cccggcagccgcccc | 23603 |
rs7315864 | snp | A/G | 0.433673 | 0.1696 | intron-variant | CORO1C | GRCh38.p7 | 12:108674443 | GTCCCAGCTACTCGG[A/G]GGGCTGAGGCAGGAG | 23603 |
rs7358571 | snp | C/T | 0.437683 | 0.165152 | intron-variant | CORO1C | GRCh38.p7 | 12:108675924 | ggacagaggagcaag[C/T]tgaactgcaacatga | 23603 |
rs7484423 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CORO1C | GRCh38.p7 | 12:108727371 | TAGAAGTAGAAAGGC[A/G]ATGAAGTAATAAATT | 23603 |
rs7952939 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CORO1C | GRCh38.p7 | 12:108699533 | GCTCCAGTGTCTGAC[C/T]TTAGCTAACAAGCTA | 23603 |
rs7955014 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108717883 | TTTGCTCGCAAAAGT[A/G]TCTGGAGCTTGAAGA | 23603 |
rs7961079 | snp | A/G | 0.245631 | 0.249962 | intron-variant | CORO1C | GRCh38.p7 | 12:108729288 | CCGAATCTAATCCTA[A/G]ACTATATATAAATAA | 23603 |
rs7961563 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671936 | cccagctaatttttt[A/T]tttttttgtagacac | 23603 |
rs7969979 | snp | A/G | 0.441568 | 0.160629 | intron-variant | CORO1C | GRCh38.p7 | 12:108714119 | ACCTGGGCCGGGCAC[A/G]GTGGCTCACACCTAT | 23603 |
rs7970075 | snp | A/C | 0.0854556 | 0.188216 | intron-variant | CORO1C | GRCh38.p7 | 12:108714112 | AAGAACAACCTGggc[A/C]gggcacagtggctca | 23603 |
rs7973091 | snp | A/G | 0.106987 | 0.205054 | intron-variant | CORO1C | GRCh38.p7 | 12:108725106 | cagacCTGAATAGAG[A/G]AGACTGTCTGAATAG | 23603 |
rs7973983 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CORO1C | GRCh38.p7 | 12:108667988 | ATACTGCTTTCCAGA[C/T]ACTGCTTCCCTATTT | 23603 |
rs7974616 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | CORO1C | GRCh38.p7 | 12:108722598 | GTCTAGGCTGGGAAC[A/G]TACCCACCACTTACA | 23603 |
rs7976646 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671935 | acccagctaattttt[A/T]atttttttgtagaca | 23603 |
rs9669138 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | CORO1C | GRCh38.p7 | 12:108725161 | AAAACACTGGAGGTG[C/T]TTTTAAGACCGCCTT | 23603 |
rs9783411 | snp | A/C | 0.319376 | 0.240181 | intron-variant | CORO1C | GRCh38.p7 | 12:108712761 | CTGAGGTGGGAAGAT[A/C]GCTTAAGGCCAGGGG | 23603 |
rs9783521 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108674120 | gtacaaggagattaa[C/T]gttgttttcacctgc | 23603 |
rs9795953 | snp | A/G | 0.395087 | 0.203592 | intron-variant | CORO1C | GRCh38.p7 | 12:108715926 | ATCACAAGGTCAGGA[A/G]ATGAGACCATCCTGG | 23603 |
rs10431414 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108688295 | CCTATATATTGAGGG[A/C]AGTACTGAGTACAAT | 23603 |
rs10450765 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644751 | GCGGCCATGCAGCGA[A/G]GGTTGTTTGTGTGGC | 23603 |
rs10450766 | snp | A/G | 0.00874735 | 0.0655527 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644850 | AGGATTAGGAACCCC[A/G]TCCCAGGACACACCG | 23603 |
rs10450767 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644856 | AGGAACCCCATCCCA[A/G]GACACACCGCTGGCA | 23603 |
rs10450768 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646736 | GGTAATATGAATCCA[C/T]GTGATTTTTCAAGTC | 23603 |
rs10507230 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108668645 | TTTAAACTTAAAAAT[C/T]TGGACTATTCTATAG | 23603 |
rs10507231 | snp | C/T | 0.184203 | 0.241186 | intron-variant | CORO1C | GRCh38.p7 | 12:108679562 | GTGCACAGAAAGGAA[C/T]CACTGCAATGTATGG | 23603 |
rs10507232 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | CORO1C | GRCh38.p7 | 12:108702242 | ATACAGCAGTAACAG[C/T]TGGGACCTAGGAAAG | 23603 |
rs10507233 | snp | G/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108709908 | CCCTTGCTTGCAACA[G/T]TAAGATCATCTCAGT | 23603 |
rs10645621 | in-del | -/GAGG | 0.432357 | 0.171014 | intron-variant | CORO1C | GRCh38.p7 | 12:108647952 | GCTCCTGCCATCTGT[-/GAGG]GAGGCTCCTTCTTGG | 23603 |
rs10652886 | in-del | -/ATA | 0.364401 | 0.222289 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732809 | ATCTGTAAAATGGGG[-/ATA]ATAACAGCCCCTCCC | 23603 |
rs10652887 | in-del | -/TAA/TAC | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732813 | GTAAAATGGGGATAA[-/TAA/TAC]CAGCCCCTCCCTCAC | 23603 |
rs10746128 | snp | C/T | 0.435407 | 0.167703 | intron-variant | CORO1C | GRCh38.p7 | 12:108663255 | CATTTGGTGGCAGAC[C/T]TTGGAAAACAGCCTG | 23603 |
rs10746129 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | CORO1C | GRCh38.p7 | 12:108697313 | TAACCTGCCTGTCTA[C/T]AACCAGAAACAAAAA | 23603 |
rs10746130 | snp | A/T | 0.436692 | 0.166271 | intron-variant | CORO1C | GRCh38.p7 | 12:108720305 | AGAAATCAATTAAGT[A/T]AATTTGTGATGAGTA | 23603 |
rs10778652 | snp | C/G | 0.488666 | 0.0744214 | intron-variant | CORO1C | GRCh38.p7 | 12:108650947 | AAAAAATCACATAGA[C/G]AGTTTTGGTTTGTTT | 23603 |
rs10778653 | snp | C/G | 0.489201 | 0.0726845 | intron-variant | CORO1C | GRCh38.p7 | 12:108688689 | AGGCAGGTGGATCAT[C/G]TGAGGTCAGGAGTTC | 23603 |
rs10778654 | snp | A/G | 0.41141 | 0.19091 | intron-variant | CORO1C | GRCh38.p7 | 12:108715144 | GAGGCTGAAGCAGGA[A/G]GATCCCTTGAGCCCA | 23603 |
rs10778655 | snp | C/T | 0.424503 | 0.179021 | intron-variant | CORO1C | GRCh38.p7 | 12:108721912 | TGTGAAGTTCCCAAA[C/T]GGAAAAGAAAAAAAA | 23603 |
rs10861956 | snp | A/G | 0.411242 | 0.191052 | intron-variant | CORO1C | GRCh38.p7 | 12:108660699 | TGTTGCTGCTGCCCT[A/G]TATTGAGCCTTGATG | 23603 |
rs10861957 | snp | C/T | 0.434976 | 0.168179 | intron-variant | CORO1C | GRCh38.p7 | 12:108662601 | TGTTAAGTTCAAAAC[C/T]CTCCAGTTAGAAGCA | 23603 |
rs10861959 | snp | A/G | 0.39527 | 0.203462 | intron-variant | CORO1C | GRCh38.p7 | 12:108674444 | TCCCAGCTACTCGGA[A/G]GGCTGAGGCAGGAGA | 23603 |
rs10861960 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108683467 | GTGGAAAAAAAATAA[A/G]TAACAAAATCAACTA | 23603 |
rs10861961 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | CORO1C | GRCh38.p7 | 12:108692019 | CAGCAAAACTGTGGA[A/T]AACACAGTCACTAGG | 23603 |
rs10861962 | snp | C/G | 0.48818 | 0.0759629 | intron-variant | CORO1C | GRCh38.p7 | 12:108692847 | CTGTCGCCCAGGCTG[C/G]AGTGCAATGGTGCTA | 23603 |
rs10861963 | snp | G/T | 0.394904 | 0.203722 | intron-variant | CORO1C | GRCh38.p7 | 12:108692861 | GGAGTGCAATGGTGC[G/T]ATCTCAGCTCACTGC | 23603 |
rs10861964 | snp | G/T | 0.40386 | 0.197046 | intron-variant | CORO1C | GRCh38.p7 | 12:108693967 | ACAAAGCACCCCCCT[G/T]GAGAGATCAAGCACA | 23603 |
rs10861965 | snp | A/G | 0.435837 | 0.167226 | intron-variant | CORO1C | GRCh38.p7 | 12:108705435 | ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAGA | 23603 |
rs10861966 | snp | A/G | 0.435837 | 0.167226 | intron-variant | CORO1C | GRCh38.p7 | 12:108705998 | TCAAGACCAGCTTGC[A/G]CAACATGGTGAAACC | 23603 |
rs11114019 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108651372 | TGTTGACTAGCATGA[A/G]AAAAAAGCCTGTCCC | 23603 |
rs11114020 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656114 | CCCGGCAGCCGCCCC[A/G]TCTGAGAAGTGAGGA | 23603 |
rs11114021 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656178 | GTGAGGAGCCCCTCC[A/G]CCCGGCAGCCGCCCC | 23603 |
rs11114022 | snp | A/G | 0.40263 | 0.198 | intron-variant | CORO1C | GRCh38.p7 | 12:108656428 | CCATCCGGGAGGGAG[A/G]TGGGGGGTCAGCCTC | 23603 |
rs11114023 | snp | A/T | 0.375 | 0.216506 | intron-variant | CORO1C | GRCh38.p7 | 12:108663261 | GTGGCAGACCTTGGA[A/T]AACAGCCTGGCAGTT | 23603 |
rs11114024 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CORO1C | GRCh38.p7 | 12:108682549 | AATAATTAAGGCAAA[C/T]GTTGACAGAACTTGA | 23603 |
rs11114025 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | CORO1C | GRCh38.p7 | 12:108695413 | AAAGGCTACCATATA[C/T]ATAGCCACCCAGTTT | 23603 |
rs11114026 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108698260 | TGCCAAAGTTATACA[C/T]TGAATTAGGGGGACA | 23603 |
rs11114028 | snp | A/G | 0.246485 | 0.249975 | intron-variant | CORO1C | GRCh38.p7 | 12:108702171 | CAAGCTCAAAGCCAG[A/G]TACTGGGCTAGGAAG | 23603 |
rs11114029 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705137 | CAAATTACTTAACCT[C/T]TCTGAGCCTCAGTTT | 23603 |
rs11114030 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705139 | AATTACTTAACCTCT[C/T]TGAGCCTCAGTTTCC | 23603 |
rs11114031 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705312 | GGTGAAACCCAGTCT[C/T]TACTAAAAATACAAA | 23603 |
rs11114032 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705457 | AGAGCAAGACCCTGT[C/T]TCAAAAAAAAAAAAA | 23603 |
rs11114033 | snp | A/G | 0.409041 | 0.192888 | intron-variant | CORO1C | GRCh38.p7 | 12:108706008 | CTTGCACAACATGGT[A/G]AAACCCCATCTCTAC | 23603 |
rs11114034 | snp | A/C | 0.436123 | 0.166908 | intron-variant | CORO1C | GRCh38.p7 | 12:108706196 | TGAATCAAAAAAAAA[A/C]AAAAAAAACAAAAAA | 23603 |
rs11114035 | snp | A/T | 0.489434 | 0.0719116 | intron-variant | CORO1C | GRCh38.p7 | 12:108709207 | TCCAAACTGTTTTTT[A/T]AAAAAAACTATAAAG | 23603 |
rs11114036 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CORO1C | GRCh38.p7 | 12:108711725 | CTACATAGGAAACAT[A/G]TAGGGTGTTAGGAGG | 23603 |
rs11114037 | snp | C/T | 0.134119 | 0.221521 | intron-variant | CORO1C | GRCh38.p7 | 12:108712642 | TAGAATACACATTCA[C/T]GAGAGAGCAGACACC | 23603 |
rs11114038 | snp | G/T | 0.231189 | 0.249291 | intron-variant | CORO1C | GRCh38.p7 | 12:108726569 | AATCCTAGCACTTTC[G/T]GAGGCTAAGGTAGGA | 23603 |
rs11114039 | snp | A/G | 0.403684 | 0.197183 | intron-variant | CORO1C | GRCh38.p7 | 12:108727919 | AACCCATTAAAAAAC[A/G]GGCAGAGCATTTGAA | 23603 |
rs11114040 | snp | A/G | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108727983 | ttcaccaaccacatg[A/G]aaagatgctcaacat | 23603 |
rs11114041 | snp | C/G | 0.441568 | 0.160629 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730353 | TCCCAAAAAAGGATG[C/G]CAGGGCCAGCGCCTC | 23603 |
rs11114042 | snp | A/G | 0.465158 | 0.127307 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730938 | GTGAGCCCGGCCCCT[A/G]CCCGCCCCCACCCAC | 23603 |
rs11114043 | snp | A/C | 0.0607341 | 0.163335 | upstream-variant-2KB, intron-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731419 | CCCCCGCCGGGCGCG[A/C]GCCGCTCACCCGGGC | 23603 |
rs11272026 | in-del | -/CAGAACCATATAAAATC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715668 | ATACTCACAACACTG[-/CAGAACCATATAAAATC]GCAGCAGCCATCTCC | 23603 |
rs11274706 | in-del | -/GCAGAACCATATAAAATCGCCTGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715667 | CATACTCACAACACT[-/GCAGAACCATATAAAATCGCCTGA]GGCAGCAGCCATCTC | 23603 |
rs11447073 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692794 | CCATTAGACCACAGC[-/T]TTTTTTTTTTTTTTT | 23603 |
rs11449783 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689050 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGGT | 23603 |
rs11547298 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678337 | ACAGGACCAGTGCTG[G/T]ACATAGACTGGTGCC | 23603 |
rs11611153 | snp | A/G | 0 | 0 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732756 | ACTAAGACAGCTATC[A/G]CAgcaaattatttat | 23603 |
rs11611166 | snp | C/T | 0.217851 | 0.247924 | intron-variant | CORO1C | GRCh38.p7 | 12:108725520 | GGGAGCTGGCAAAGT[C/T]ACAGCTAGCAAGAAG | 23603 |
rs11611236 | snp | A/G | 0.217851 | 0.247924 | intron-variant | CORO1C | GRCh38.p7 | 12:108725640 | ACGAGAACTACAGAA[A/G]GTACCCATAGCTCAC | 23603 |
rs11613321 | snp | A/T | 0.217851 | 0.247924 | intron-variant | CORO1C | GRCh38.p7 | 12:108725579 | CTGGCCCTAAAGGCC[A/T]GCACCCTCACGGCCT | 23603 |
rs11614170 | snp | A/T | 0.225893 | 0.248835 | intron-variant | CORO1C | GRCh38.p7 | 12:108681407 | TCTTATCTATTCATA[A/T]CCTAGTGCAATTTAG | 23603 |
rs11830250 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108653957 | CATAAGTACAGATAA[A/G]TCTAAAATCACCAAT | 23603 |
rs11835024 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664330 | GTTTTCAATTGCTTA[C/G]TGGAAGGCAGAGATC | 23603 |
rs12298235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700635 | TTTTCTTGAGTTCTT[C/G]TTCCATTTCCAACTC | 23603 |
rs12301079 | snp | C/G | 0.230896 | 0.249269 | intron-variant | CORO1C | GRCh38.p7 | 12:108677118 | AGTAGCATGGTTCTC[C/G]AATGCTGACACGTGC | 23603 |
rs12310514 | snp | C/T | 0.133777 | 0.221342 | intron-variant | CORO1C | GRCh38.p7 | 12:108709023 | gccttccaaactgct[C/T]ggattataggcatta | 23603 |
rs12310647 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108712361 | ggtggattgcccgaa[C/T]tcaggaattcgagac | 23603 |
rs12310699 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712461 | tgcctgtaatcccag[C/T]tactcaggaggctga | 23603 |
rs12311748 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728491 | atggggtttcttttt[G/T]ggggggatgaaaatg | 23603 |
rs12312512 | snp | G/T | 0.108402 | 0.206034 | intron-variant | CORO1C | GRCh38.p7 | 12:108688946 | tgaggcaggagaatt[G/T]cttgagcctgggaga | 23603 |
rs12316020 | snp | C/T | 0.224709 | 0.248717 | intron-variant | CORO1C | GRCh38.p7 | 12:108720668 | agctgggactacagg[C/T]gcccgccaccacgcc | 23603 |
rs12316028 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720687 | cgccaccacgcccgg[C/T]taattttttgtattt | 23603 |
rs12319291 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732461 | ctcagctctgcggcc[A/G]tcagactgtgtgacc | 23603 |
rs12322587 | snp | C/T | 0.00331674 | 0.0405878 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704646 | CTGAGTCAGGCATCT[C/T]TAAGCGGAGCTTGAA | 23603 |
rs12368018 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | CORO1C | GRCh38.p7 | 12:108699812 | TAATGAAAAGATTCA[C/T]CTTCGCCAATAAGAA | 23603 |
rs12370950 | snp | A/C | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730186 | AATTTGCTTCGCACT[A/C]TGAATCCCACGTTTG | 23603 |
rs12371090 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720175 | tgggtgacagagcaa[A/G]accctgtctcaaaca | 23603 |
rs12423307 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108668905 | AGTAAAATACTTAGG[C/T]AGCCACAATCTTAAA | 23603 |
rs12423733 | snp | C/T | 0.189576 | 0.242588 | intron-variant | CORO1C | GRCh38.p7 | 12:108724213 | AACTGAAGAAAACTC[C/T]GTGAATAGGCTTGGT | 23603 |
rs12424752 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108675027 | ttttgtgagaggcca[A/G]gtcaatcagtatgac | 23603 |
rs12426771 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697798 | TGCTGGCACACAGCA[A/G]GTACTCTGCTTACAG | 23603 |
rs12427083 | snp | C/T | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108719465 | TCCTAAGCGATTAGA[C/T]CATTTTAACAGTTGT | 23603 |
rs12578143 | snp | G/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108669500 | TATGGAAGGCAACTG[G/T]GGCTGAGAGCGTTTA | 23603 |
rs12579105 | snp | G/T | 0.411074 | 0.191194 | intron-variant | CORO1C | GRCh38.p7 | 12:108693078 | GCTGGAATTACAAGC[G/T]TGAGCCACCGCGCCC | 23603 |
rs12580445 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108681581 | TAAGAAAAACCACCA[C/T]CCTTGTATTCCATAC | 23603 |
rs12581386 | snp | A/C | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108689223 | CAAAAAAAGATGGAT[A/C]AATCTGATAATCACT | 23603 |
rs12582815 | snp | A/C | 0.195214 | 0.243923 | intron-variant | CORO1C | GRCh38.p7 | 12:108723602 | TTGAGACATGGGGAC[A/C]CACACCCAGTTCCAC | 23603 |
rs12812516 | snp | G/T | 0.0879795 | 0.190393 | intron-variant | CORO1C | GRCh38.p7 | 12:108687718 | tgaacctgggaggca[G/T]aggtttcagtgagcc | 23603 |
rs12821621 | snp | A/C | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108722683 | TAACTGAGTTAGACT[A/C]TGGAACACAACCCAG | 23603 |
rs12821861 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655343 | TTTAAAAAATATAGT[C/G]CCCTCCCTctcccct | 23603 |
rs17040848 | snp | C/T | 0.140581 | 0.224783 | intron-variant | CORO1C | GRCh38.p7 | 12:108677183 | TTAATTAGAGACCAT[C/T]TTCCCTTATTTCAGG | 23603 |
rs17040852 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108679552 | TTAAGAGCAGGTGCA[C/T]AGAAAGGAACCACTG | 23603 |
rs17040859 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | CORO1C | GRCh38.p7 | 12:108682515 | ATAAACTGTAATTCA[C/T]CTAACCATATAATTT | 23603 |
rs17040860 | snp | C/T | 0.193028 | 0.243422 | intron-variant | CORO1C | GRCh38.p7 | 12:108686254 | GATTGTGAGGGGCCA[C/T]TCAGAAAGACATCCA | 23603 |
rs17040862 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108686329 | GCAAATTTAAATGAA[C/T]GCAGAGGCTGAAAGG | 23603 |
rs17040863 | snp | C/G | 0.0152663 | 0.0860237 | intron-variant | CORO1C | GRCh38.p7 | 12:108689216 | GAAAAAACAAAAAAA[C/G]ATGGATCAATCTGAT | 23603 |
rs17040870 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108691634 | CACCATTCTCTGAGC[C/T]ACCCGTGCAGCCAAT | 23603 |
rs17040872 | snp | C/T | 0.186737 | 0.241863 | intron-variant | CORO1C | GRCh38.p7 | 12:108693217 | AACCTAAGTTCTAAT[C/T]CACAAACAACCTCAC | 23603 |
rs17040877 | snp | C/G | 0.186105 | 0.241697 | intron-variant | CORO1C | GRCh38.p7 | 12:108693426 | TAAAGATGATACAAA[C/G]GAAAGACGCCATGTT | 23603 |
rs17040884 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108695521 | TTAATAATGTGATAA[C/T]GCAGGCTGTGGTACC | 23603 |
rs17040894 | snp | C/T | 0.184203 | 0.241186 | intron-variant | CORO1C | GRCh38.p7 | 12:108698941 | TCATGAACCTATCGA[C/T]TATAGAAACCCAAGT | 23603 |
rs17040895 | snp | C/T | 0.184203 | 0.241186 | intron-variant | CORO1C | GRCh38.p7 | 12:108699937 | CACTGAAGTAAAAAT[C/T]AGATGTTATAATAAA | 23603 |
rs17040909 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108710883 | TTTTCTTACATGTTG[C/G]GTGAATATTTTAACC | 23603 |
rs17040915 | snp | A/C | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108722068 | GGTCTGCCTGACTTC[A/C]CATGCCTCTGCTCAA | 23603 |
rs28408449 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655171 | CGACACATGTACACA[A/G]AGATTGAGATGATAG | 23603 |
rs28529616 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707894 | TGCTGGACATCATTA[A/G]TCAATGGAGAAATGA | 23603 |
rs34025914 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670272 | GGGACACCTGACAGA[-/C]CTGAGGGCAGCAGGC | 23603 |
rs34108470 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715547 | AAACACAACCACCTC[-/T]TTTTGGTCCCTGGAG | 23603 |
rs34115561 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674921 | AGTTGATAAGGCAGC[-/A]AAAGGGTTTGAGAGG | 23603 |
rs34122937 | in-del | -/A | 0.432063 | 0.171327 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647042 | TGGTCCCTATTCATT[-/A]AAAAAAAAAGGGTAC | 23603 |
rs34182326 | in-del | -/A/AA | 0.499824 | 0.00938333 | intron-variant | CORO1C | GRCh38.p7 | 12:108714397 | GCGAGAGTCAGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 23603 |
rs34199304 | in-del | -/A | 0.217851 | 0.247924 | intron-variant | CORO1C | GRCh38.p7 | 12:108728342 | TATTATTTGACCATT[-/A]AAAAAAAAAAATGAA | 23603 |
rs34254734 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703438 | ACATGAAAGGACAAG[-/C]AGGACTGGAAAAGAG | 23603 |
rs34285595 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662822 | AAAAGAAAAAAATGA[-/C]ATTAGACCTCATCAA | 23603 |
rs34292438 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO1C | GRCh38.p7 | 12:108699495 | GGGAAATAAAAACTC[A/G]TAACTCCAAAACAAA | 23603 |
rs34330834 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679583 | AATGTATGGCTTAAT[-/C]CTATTTTTTGTTGTT | 23603 |
rs34430227 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CORO1C | GRCh38.p7 | 12:108714265 | GTGGTGGCGCACAAC[C/T]GTAGTCCCAGCTACT | 23603 |
rs34448583 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722693 | GACTCTGGAACACAA[-/C]CCCAGTCTTGAGTTG | 23603 |
rs34606032 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720537 | GAATTTTTTTTTTTT[-/T]ATTTGAGATGGAGTC | 23603 |
rs34743822 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710099 | GTAATTTATCACTCT[-/C]CCTCCTATTTTCCAA | 23603 |
rs34776902 | snp | C/G | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730402 | TTTCTTCTCAGCTCT[C/G]ACCGCAGCCTGCCAC | 23603 |
rs34799202 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665818 | TGATGTGACTGAATT[-/C]CTGATTCAGTCACAT | 23603 |
rs34807033 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702483 | AGATCACCAGGCCCT[-/C]CCCTGATTAAGATTT | 23603 |
rs34822039 | in-del | -/A | 0.169435 | 0.236663 | intron-variant | CORO1C | GRCh38.p7 | 12:108671465 | ACAGGAAAAAAAAAA[-/A]TTAAAAACTGTAATG | 23603 |
rs34827230 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669673 | CAGAGCTTTTCCGTT[-/A]AAAAAAAAAAAAAAA | 23603 |
rs34841535 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700743 | ATTTCTGCCCATTTG[-/A]AAAATGTAACTGTTT | 23603 |
rs34887047 | in-del | -/C | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644833 | AGAAAAGGGACTCAG[-/C]AAGGATTAGGAACCC | 23603 |
rs34893627 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720555 | TGAGATGGAGTCTCT[-/C]CTTTGTTGCCCAGGC | 23603 |
rs34898518 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650466 | TTACAGGGTGAACCA[-/C]CCACTCCTGGCCCAA | 23603 |
rs34941792 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108705482 | AAAAAAAAAAAAAAA[A/G]GAATGTAAACCAACC | 23603 |
rs34955160 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652474 | AAACATCTGGATTAT[-/G]GGGGGTGTCTCTCTC | 23603 |
rs34961869 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699441 | CCATTTCTTTGAAGG[-/A]AAAAAAAAGTCTTAC | 23603 |
rs34979355 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | CORO1C | GRCh38.p7 | 12:108722209 | AAAGGGTTAAAGAAC[A/C]TGAGTGAAATGACAT | 23603 |
rs35005278 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728490 | ATGGGGTTTCTTTTT[-/G]GGGGGGGATGAAAAT | 23603 |
rs35021885 | in-del | -/G | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658758 | AATCTCTTGTTTCCT[-/G]GGGATCAATGACTCT | 23603 |
rs35067523 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645249 | GGGATGTCATGGCTT[-/A]AAAAAAAAAAAAAAA | 23603 |
rs35103901 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702335 | ATCCACCACAGCCAC[-/T]TTCCCTAGTAAACCA | 23603 |
rs35221821 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673453 | ATAAAAGTACAAGGG[-/C]AAAGCAGCAAGTGCT | 23603 |
rs35233071 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713262 | GATATGGACTTGTTG[-/A]AAAAAATGTTTTTTC | 23603 |
rs35299953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108676564 | ATCACTTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 23603 |
rs35335898 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675759 | ACAGAATACACAAAT[-/G]GGAAAAAGGATGAAA | 23603 |
rs35410135 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651219 | TTAATTGTGAGACCA[-/G]GAACAGCAAGCGTTT | 23603 |
rs35418727 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665820 | ATGTGACTGAATTCC[-/T]GATTCAGTCACATAG | 23603 |
rs35452794 | in-del | -/A/AAAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679170 | GAAATTTAAAAAGTT[-/A/AAAA]AAAAAAAAAAAAAAA | 23603 |
rs35502116 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709486 | AAAATTGGGAACTAT[-/C]CCCAAACACAAAAAC | 23603 |
rs35573294 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653548 | ATTTATTTCAACTAC[-/A]AAAAGTTCTAAGGGA | 23603 |
rs35637732 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670653 | CCATTTAAAAAGCTT[-/G]GGGAAAATTAAATCC | 23603 |
rs35685734 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700462 | GCAGGCTTTCTGGGA[-/G]GGATAAAGGAAGGAG | 23603 |
rs35744002 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679879 | TGATACTTATTAACT[-/C]CCCACAATTACCGTA | 23603 |
rs35852984 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723291 | TAAATCAGTCAATTC[-/T]TTTAAGTTCCTAAGA | 23603 |
rs35885046 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714245 | ATACAAAAATTAGCA[-/G]GGGCGTGGTGGCGCA | 23603 |
rs35887254 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696238 | TTTCACAATACTCAA[-/G]GGAAGGAAGGGAGAA | 23603 |
rs35894267 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701516 | CAAAATGCGTCAGGG[-/A]AAAGAATTACAAAGA | 23603 |
rs35984712 | in-del | -/A | 0.498908 | 0.0233371 | intron-variant | CORO1C | GRCh38.p7 | 12:108689032 | GAGACTCTGTCTCAG[-/A]AAAAAAAAAAAAAAA | 23603 |
rs36060769 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711518 | AACCCCATGTCTACT[-/A]AAAATACAAAAATTA | 23603 |
rs55660433 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108685575 | CCAACCATACTAGAT[C/T]TGGATAGGGAAAGAA | 23603 |
rs55721100 | snp | A/C | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108728878 | AGGAGACAGTAACAC[A/C]GAGAAGTCATAAATG | 23603 |
rs55756843 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108699020 | TCACCTCCTCTAAAA[C/T]AAACTCATATTTAAG | 23603 |
rs55939346 | snp | A/G | 0.40386 | 0.197046 | intron-variant | CORO1C | GRCh38.p7 | 12:108691113 | GGGGTGGGAGGGGCT[A/G]ATGCCTTGGGCTCCA | 23603 |
rs55980422 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CORO1C | GRCh38.p7 | 12:108653278 | TCTGAGTAACTGCTC[A/G]TTTTGTTTGTTTTAA | 23603 |
rs56001016 | in-del | -/AAATAACAAAAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683476 | AATAAATAACAAAAT[-/AAATAACAAAAT]CAACTAAACTGGATA | 23603 |
rs56011926 | in-del | -/A | 0.350764 | 0.228794 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704471 | CAAAAAAAAAAAAAA[-/A]GTTATTTCCATATTA | 23603 |
rs56049020 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720237 | ACTTGCTAACCAGAG[C/T]TATAAAATACAGCCA | 23603 |
rs56092188 | snp | A/G | 0.17332 | 0.23795 | intron-variant | CORO1C | GRCh38.p7 | 12:108655721 | CAGTGGTGTGATCTC[A/G]GCTAGCTACAACCTC | 23603 |
rs56204306 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108728767 | CTAGGTACTAGGTCA[C/T]ACTGAAATATTCATG | 23603 |
rs56216117 | in-del | -/GTAT | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108729389 | AGTTATGTTTCATCG[-/GTAT]GTATCTATTAAAATT | 23603 |
rs56342329 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | CORO1C | GRCh38.p7 | 12:108719308 | ATGGTTTATGGTACC[A/C]TCAAAAAACTACCAG | 23603 |
rs56354906 | snp | C/T | 0.171704 | 0.237423 | intron-variant | CORO1C | GRCh38.p7 | 12:108677909 | CTGTAATCCCAATTA[C/T]TCGGGAGGCTGAGGC | 23603 |
rs56364122 | snp | C/T | 0.43655 | 0.16643 | intron-variant | CORO1C | GRCh38.p7 | 12:108666850 | CATGCCCCAAAGCAC[C/T]ACCCTAATAGGAAAT | 23603 |
rs56366996 | snp | C/T | 0.440884 | 0.161442 | intron-variant | CORO1C | GRCh38.p7 | 12:108691080 | TGATAAATAGAAAAA[C/T]ATTACAACTTTTTTT | 23603 |
rs56389244 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108683396 | TGCACTCCAGTCCGG[A/G]CAACAGTGCAAGACT | 23603 |
rs57173285 | in-del | -/CACAG/CACAGACCTAAGGGC/CACAGACCTAAGGGCACCA | 0.394721 | 0.203852 | intron-variant | CORO1C | GRCh38.p7 | 12:108652845 | TAACGCAATGCTGTT[lengthTooLong]ATGCCAGTATGATGA | 23603 |
rs57182728 | snp | C/T | 0.21875 | 0.248039 | intron-variant | CORO1C | GRCh38.p7 | 12:108674328 | CCAAGGCGGGCGGAT[C/T]GCGAGATCAGGAGAT | 23603 |
rs57224191 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691948 | AAGTTCCTTCTGCCA[A/G]GACTTTGTGCTCCAT | 23603 |
rs57315277 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674038 | ATCAGGAAAAAAAAA[-/AA]GATTCCTTACAAAAT | 23603 |
rs57477152 | in-del | -/ACCAATAC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652849 | GCAATGCTGTTATGC[-/ACCAATAC]CAGTATGATGATAAA | 23603 |
rs57681690 | in-del | -/ATTC | 0.411074 | 0.191194 | intron-variant | CORO1C | GRCh38.p7 | 12:108655097 | TAAAAATCATTCCAT[-/ATTC]CAAAATCCTACAGCC | 23603 |
rs58103586 | in-del | -/CC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652846 | AACGCAATGCTGTTA[-/CC]TGCCAGTATGATGAT | 23603 |
rs58174892 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669690 | AAAAAAAAAAAAAAA[-/A]GGCGGGGGGTGGCGG | 23603 |
rs58319299 | in-del | -/AAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700893 | CAACATCGTTATAAT[-/AAT]TTTTTCATCCATAGA | 23603 |
rs58536250 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659361 | CTATTAGGCAAATAC[A/G]CTCCTTCCTTTTAAA | 23603 |
rs58733894 | snp | G/T | 0.219049 | 0.248077 | intron-variant | CORO1C | GRCh38.p7 | 12:108669463 | CTCTCGATAGGCATA[G/T]TATTATCATACCTCC | 23603 |
rs58845281 | in-del | -/A | 0.481932 | 0.0933148 | intron-variant | CORO1C | GRCh38.p7 | 12:108718370 | TGAGACTCCGTCTCG[-/A]AAAAAAAAAAAAAAT | 23603 |
rs59746177 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718329 | GCTGAAATCGCACTA[C/T]TGCACTCCAGCCTGG | 23603 |
rs60044610 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701977 | TCACTACCAAACCGC[C/T]TAGTGCTAAGTGGTA | 23603 |
rs60138475 | in-del | -/GAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652853 | TGCTGTTATGCCAGT[-/GAG]ATGATGATAAAAAGT | 23603 |
rs60459711 | in-del | -/GCAC | 0.395453 | 0.203331 | intron-variant | CORO1C | GRCh38.p7 | 12:108652852 | ATGCTGTTATGCCAG[-/GCAC]TATGATGATAAAAAG | 23603 |
rs60501120 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | CORO1C | GRCh38.p7 | 12:108708319 | AAAAAGGAATGAAGT[A/G]CTAATACATGCTACA | 23603 |
rs60647143 | in-del | -/AAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694302 | AAAAAAAAAAAAAAA[-/AAA]GCAAGAACCCACCAC | 23603 |
rs60922936 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674572 | AAAAAAAAAAAAAAA[-/AA]CCTTCTGGAAAGGAT | 23603 |
rs61189340 | in-del | -/AAGG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652847 | ACGCAATGCTGTTAT[-/AAGG]GCCAGTATGATGATA | 23603 |
rs61257887 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714822 | TACTTTTTAAAGTTT[C/T]CAAAGAAGAGCACTC | 23603 |
rs61278984 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723010 | ACAGTTACTCTATTT[C/G]TAAAACAGACAACGT | 23603 |
rs61934127 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656203 | CGCCCCGTCTGAGAA[A/G]TGAGGAGCCCCTCCG | 23603 |
rs61934128 | snp | A/G | 0.154661 | 0.231107 | intron-variant | CORO1C | GRCh38.p7 | 12:108660847 | GTGATTATAAAAAAC[A/G]TGGCATCTTTTTTGA | 23603 |
rs61934129 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666873 | TAGGAAATACTGCAA[C/T]TAGGGAGAAGAGCAT | 23603 |
rs61934130 | snp | C/T | 0.140242 | 0.224618 | intron-variant | CORO1C | GRCh38.p7 | 12:108671800 | ATTGGTCTCACTCTG[C/T]TAACCAGGCTGTAGT | 23603 |
rs61934131 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | CORO1C | GRCh38.p7 | 12:108683765 | CCAATCAATCAATCA[A/T]TCAGCAAATACCAAA | 23603 |
rs61934132 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698042 | AACCAGCCAGCATCT[A/C]AGGTAGGAACAGCAA | 23603 |
rs61934133 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730893 | GCCCTCGCCCCTCCC[G/T]ACGCAGGGCCCAGCT | 23603 |
rs66526882 | in-del | -/ATA | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732810 | TCTGTAAAATGGGGA[-/ATA]TAACAGCCCCTCCCT | 23603 |
rs66537703 | in-del | -/GAGG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647953 | CTCCTGCCATCTGTG[-/GAGG]AGGCTCCTTCTTGGG | 23603 |
rs71454745 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108651776 | TGAGGTATTAATTCC[A/C]CAGTACACACAAGGA | 23603 |
rs71454746 | snp | C/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108654073 | ACCCCAGCCCAACCT[C/T]TGCTTCAGTCAAAAG | 23603 |
rs71454747 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730472 | TGGGGAGCGTGCGCC[C/G]GTGGGGACAGGCGGG | 23603 |
rs71906647 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714398 | CGAGAGTCAGTCTCA[-/A]AAAAAAAAAAAAAAA | 23603 |
rs72517995 | in-del | -/TAA | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732812 | TGTAAAATGGGGATA[-/TAA]ACAGCCCCTCCCTCA | 23603 |
rs73191261 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108694923 | TACAGTCTAAGAATA[C/T]ATGTATTAGTTATCA | 23603 |
rs73193433 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | CORO1C | GRCh38.p7 | 12:108729532 | AATCCTCAGTACACA[A/C]GACTAACCTCCACCA | 23603 |
rs73406572 | snp | A/G | 0.0166325 | 0.0896639 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645032 | TGCTCGTCCACCAAA[A/G]TCAGAGAAGCTATGT | 23603 |
rs73406576 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | CORO1C | GRCh38.p7 | 12:108651271 | TGTTACACAAATGTT[C/T]GGTACGACCTTATAT | 23603 |
rs73406580 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CORO1C | GRCh38.p7 | 12:108663634 | TCCAGAATAGGCAAA[C/T]CCGTAAAGACAGAAA | 23603 |
rs73406584 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108666088 | ACCCAGGAGGGCTCC[C/T]TGAGGAGGTGACCTC | 23603 |
rs73406587 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | CORO1C | GRCh38.p7 | 12:108670068 | AGTGGCAGCATTTTT[G/T]GGGGGTTTTTCCGAA | 23603 |
rs73406589 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CORO1C | GRCh38.p7 | 12:108671700 | CAGCAACACCTATGC[C/T]AAAAGAAAATGGAAT | 23603 |
rs73406593 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108687804 | AATAATAACAATTTA[A/G]TTAAAATTAAAAAAA | 23603 |
rs73406596 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108689370 | TGATAAAAAGTGACA[C/T]ATTCATTCGAGTGAT | 23603 |
rs73406602 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | CORO1C | GRCh38.p7 | 12:108694320 | GCAAGAACCCACCAC[A/G]GGTCGCTGCACATGC | 23603 |
rs73408606 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | CORO1C | GRCh38.p7 | 12:108715039 | AATGAGCAGCAAAAC[A/G]GTAACACATAATGAA | 23603 |
rs74325719 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108686353 | TGAAAGGAAGATGTA[C/T]AAGAATTAAAGCCAG | 23603 |
rs74390014 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108711680 | GCAAAACTCCGTCTC[A/C]AAAAAAAAAAAAAAA | 23603 |
rs74577410 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108726441 | CAAAAAAAAAAAAAA[A/T]GAACATAAGAACACA | 23603 |
rs74626141 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704471 | AGCAAGATTCCATCT[A/C]AAAAAAAAAAAAAAG | 23603 |
rs74792606 | snp | G/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108662327 | AGGCGGTTTTTTTTT[G/T]GTTTGTTTTTTTGTT | 23603 |
rs74839415 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108726668 | TTAAAAAAAAAAAAA[A/G]AGAATGAAAAGAAAG | 23603 |
rs74877702 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CORO1C | GRCh38.p7 | 12:108686299 | GACAACACAGTTTAC[C/T]TGAACCTCTAAGCAG | 23603 |
rs74921457 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108717443 | CATTTTAAAAGCTCA[C/T]GCTGAATGAAGCTGG | 23603 |
rs74939224 | snp | C/T | 0.165853 | 0.235413 | intron-variant | CORO1C | GRCh38.p7 | 12:108657192 | TCTAAGACAATCAGG[C/T]GTTTAGAAAACTACA | 23603 |
rs74964400 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CORO1C | GRCh38.p7 | 12:108702972 | CTTTGGTAGAGGAGA[C/T]GGCAAATGATTCGTG | 23603 |
rs75007254 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710946 | GTTTAAAGGCTTTAT[G/T]TGTCAGAGAAAATTT | 23603 |
rs75029844 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108695566 | GCAACTAAGAGAACC[C/G]AATGGATGAGTTCCT | 23603 |
rs75118053 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | CORO1C | GRCh38.p7 | 12:108666524 | GCCTGTCATTATGTG[C/G]CTCTCTGCCCTCTTC | 23603 |
rs75258935 | snp | A/T | 0.1652 | 0.235179 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659436 | TATAGAGAACATATA[A/T]AAACAAAAGGAAAAA | 23603 |
rs75283310 | snp | C/T | 0.00343735 | 0.0413141 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648836 | AGGATACAGGTCATC[C/T]TGGAAAAGGTCAGAC | 23603 |
rs75326273 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108664258 | TCAACACTAGAACAC[A/G]TGAGAAAAAGAATTT | 23603 |
rs75435485 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108683071 | AAATTAATGCATTGA[A/G]TTGCTACCTTGAGAA | 23603 |
rs75522117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716883 | TCCCAGTCATTCTTT[G/T]GTTCAACAACTATTC | 23603 |
rs75568220 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CORO1C | GRCh38.p7 | 12:108679868 | AATAGTTAACAATGA[C/T]ACTTATTAACTCCCA | 23603 |
rs75623388 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108659852 | CTGCTCTGATCATGG[G/T]GAGAAGCCCAAACTG | 23603 |
rs75642916 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108705847 | TTAACGTAACACATT[A/G]TATCAATAGAAGAAA | 23603 |
rs75718483 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108683459 | AGAAGTCAGTGGAAA[A/C]AAAATAAATAACAAA | 23603 |
rs75743103 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CORO1C | GRCh38.p7 | 12:108693210 | ACTCAGCAACCTAAG[C/T]TCTAATTCACAAACA | 23603 |
rs75787928 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108678944 | GGTGAAACCCCACCT[C/T]TACTAAAAATACAAA | 23603 |
rs75792705 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108709637 | TATCAGCTATATTGT[A/C]CCAAACTGATCAAAT | 23603 |
rs75809436 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108692156 | TGGTGCCCTCCCCCT[C/G]CATCCTCCACCCCTC | 23603 |
rs75869638 | snp | G/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108687937 | CCCTTTTTTTTTTTT[G/T]GAGACGGAGTCTCAC | 23603 |
rs75932124 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108726440 | TCAAAAAAAAAAAAA[A/T]TGAACATAAGAACAC | 23603 |
rs76001896 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | CORO1C | GRCh38.p7 | 12:108721251 | GTATAAATGCATAAC[C/T]TATTATCATCACTTT | 23603 |
rs76006517 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108694282 | GCAAGACTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 23603 |
rs76030883 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | CORO1C | GRCh38.p7 | 12:108711897 | TGAAAAGCTATCTGT[G/T]TAAAGATTCCAGCAG | 23603 |
rs76064301 | snp | G/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108687936 | ACCCTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA | 23603 |
rs76069359 | snp | C/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108693856 | AGGAAAAAAAAAAAC[C/T]TGAATTCAAACCGAA | 23603 |
rs76107243 | snp | C/G | 0.0329836 | 0.124112 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731933 | TTAGCTCCTCTGAGC[C/G]CCGCGCACTGCCTAT | 23603 |
rs76144031 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CORO1C | GRCh38.p7 | 12:108725627 | AAACTCTCTTAGAAC[A/G]AGAACTACAGAAGGT | 23603 |
rs76226566 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108693854 | AGAGGAAAAAAAAAA[A/C]CCTGAATTCAAACCG | 23603 |
rs76470314 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108722538 | GAATTCCACTATCAC[A/C]ATAAACAATTTCAAA | 23603 |
rs76470389 | snp | C/T | 0.003504 | 0.04171 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647481 | TGTGTCTTTTATAGA[C/T]TTGATCTCTTTTAAA | 23603 |
rs76482184 | snp | C/T | 0.164219 | 0.234823 | intron-variant | CORO1C | GRCh38.p7 | 12:108691072 | GGTGGAGATGATAAA[C/T]AGAAAAATATTACAA | 23603 |
rs76489124 | snp | A/G | 0.11228 | 0.208646 | intron-variant | CORO1C | GRCh38.p7 | 12:108726667 | ATTAAAAAAAAAAAA[A/G]AAGAATGAAAAGAAA | 23603 |
rs76545327 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108648921 | GAATTTTATTTTTAC[A/T]TTTGTTTAAAATATG | 23603 |
rs76628739 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108702280 | GCAGGGGCTATTGTC[A/G]GGGGGAAACAAAACC | 23603 |
rs76764140 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682189 | GACAAATTTTTTAAG[-/A]AAAAAAAGCATGAAA | 23603 |
rs76824355 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | CORO1C | GRCh38.p7 | 12:108722946 | ACTTATCTTTTCCTA[C/T]AGTAGCACTGTAAAG | 23603 |
rs76826111 | snp | A/G/T | 0.00954224 | 0.0684493 | intron-variant | CORO1C | GRCh38.p7 | 12:108693263 | CTCAATTTGGTTTCA[A/G/T]TTTCTACAACTGTAG | 23603 |
rs76900183 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108719715 | TTTAATGACAATAGC[A/G]CATTAAAGGATGAGA | 23603 |
rs76904670 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108680620 | AAAACTAGAATGTTT[A/C]ACAGTTTATTCCTTA | 23603 |
rs76908343 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647957 | CTGCCATCTGTGAGG[C/G]TCCTTCTTGGGAGGG | 23603 |
rs76968863 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108705463 | AGACCCTGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 23603 |
rs76991074 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108716391 | GGGGGATATTTTTAT[C/T]AATAACTTCATAAGG | 23603 |
rs77000390 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CORO1C | GRCh38.p7 | 12:108712305 | AGGCCGGGCAGGGCG[A/G]CTCACACCTGTAAAT | 23603 |
rs77103653 | snp | A/G | 0.164546 | 0.234942 | intron-variant | CORO1C | GRCh38.p7 | 12:108671385 | TGGAGAGAAACTGAC[A/G]ATGACTAAAGAGAAG | 23603 |
rs77142765 | snp | A/G | 0.21875 | 0.248039 | intron-variant | CORO1C | GRCh38.p7 | 12:108698233 | GCAGCCAGGAGTAAA[A/G]AGGCATCTACTTGCC | 23603 |
rs77223355 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | CORO1C | GRCh38.p7 | 12:108677367 | TTCACACATAACCTA[C/T]TTTTGGAAACTAAAG | 23603 |
rs77230475 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108663310 | AGTTATCATATGATC[C/T]GGTAATTCCACTCCT | 23603 |
rs77251940 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | CORO1C | GRCh38.p7 | 12:108681129 | CCTCAGCCTCCTACA[C/T]AGCTGGAACTATAGG | 23603 |
rs77272046 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108727495 | TCAGAGCCCACCTTA[C/T]TCCACACCTCATTAA | 23603 |
rs77288681 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | CORO1C | GRCh38.p7 | 12:108651370 | TTTGTTGACTAGCAT[A/G]AGAAAAAAGCCTGTC | 23603 |
rs77329155 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108652519 | CAGTAGTTGGGACCC[C/T]GCTTCAGTAGCTGAC | 23603 |
rs77331697 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108700574 | ACTGTTTAAATCCTA[C/T]GCTGAAACTTACTAT | 23603 |
rs77333281 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108730052 | TATTTCCAAAAGTAA[A/G]TATATTCGCCACCCA | 23603 |
rs77347480 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108698243 | GTAAAAAGGCATCTA[C/T]TTGCCAAAGTTATAC | 23603 |
rs77395454 | snp | C/T | 0.222928 | 0.24853 | intron-variant | CORO1C | GRCh38.p7 | 12:108686791 | GGGACATTGGTGAAA[C/T]AGGTCAGGACACTGG | 23603 |
rs77494503 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704306 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 23603 |
rs77573034 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108650937 | AACTAAAAAAAAAAA[A/T]TCACATAGAGAGTTT | 23603 |
rs77588813 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702328 | AGCTGATCATCCACC[A/C]CAGCCACTTCCCTAG | 23603 |
rs77604030 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | CORO1C | GRCh38.p7 | 12:108662365 | TTTCGTTTTTGAGAC[A/G]GAGTCTCACACTGTT | 23603 |
rs77610543 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | CORO1C | GRCh38.p7 | 12:108702647 | AATCAGATCCTCATA[C/T]ACAGAGGAGAGCTAA | 23603 |
rs77619603 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108726428 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAATGA | 23603 |
rs77635580 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108652026 | CCAGACTCCGTCTCA[A/C]AAAAAAAAAAGTGAG | 23603 |
rs77715832 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108712179 | AGAAGAGATCCGATG[C/T]GTTATTCAATAGAAA | 23603 |
rs77736783 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CORO1C | GRCh38.p7 | 12:108676353 | CTATTTGGTGTGTTT[C/T]TCTGTTTTATAATAC | 23603 |
rs77747402 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | CORO1C | GRCh38.p7 | 12:108648548 | CTGGACCACAAGGGC[C/T]TTCTAGAGGATAAAG | 23603 |
rs77830776 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732814 | GTAAAATGGGGATAA[C/T]AGCCCCTCCCTCACA | 23603 |
rs77866012 | snp | A/G | 0.195526 | 0.243993 | intron-variant | CORO1C | GRCh38.p7 | 12:108721979 | TCACTGTTTTGGAGT[A/G]ACAGGAAGAACCTTT | 23603 |
rs77934196 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108728354 | ATTAAAAAAAAAAAA[A/T]GAAGTACTATACAAT | 23603 |
rs77952767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108672229 | AGATTGACACAATGA[C/T]TGATGGAGAGTACTT | 23603 |
rs78037690 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704623 | GCCAGTGCTTCCGCA[G/T]TGCTGTGCTGAGTCA | 23603 |
rs78091339 | snp | A/C | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108662916 | GGAGAAAATAACTTA[A/C]AAATCATACATTTGA | 23603 |
rs78136895 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108727872 | TTGAATCTAGAATAC[A/G]TGAACAACTTTTATA | 23603 |
rs78181570 | snp | A/G | 0.190519 | 0.242821 | intron-variant | CORO1C | GRCh38.p7 | 12:108684139 | ATGGGCAAATTACAC[A/G]AGCAGAGAACTCACA | 23603 |
rs78197408 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108661265 | TTCTGTACAACACCA[A/G]TGTCCAGAAATAGGG | 23603 |
rs78224947 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | CORO1C | GRCh38.p7 | 12:108722506 | TCTTTCACATGACTA[C/T]CAGCTCCCAAGATCC | 23603 |
rs78317425 | snp | C/T | 0.133093 | 0.220981 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704450 | GCACTCCAGCCTGGG[C/T]GACATAGCAAGATTC | 23603 |
rs78457084 | snp | G/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108713024 | AAGAATTTACCTAAC[G/T]AATTGCATATTTCTA | 23603 |
rs78466702 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108657068 | AAATTAAAAAAAATT[A/T]AAAAAATAAAAAATA | 23603 |
rs78566873 | snp | C/G/T | 0.00398763 | 0.0445073 | intron-variant | CORO1C | GRCh38.p7 | 12:108690629 | TGCCCAAATATGCGA[C/G/T]AGCAACCAGAGTAGC | 23603 |
rs78603070 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108693844 | GCTCCTACGCAGAGG[A/G]AAAAAAAAAACCTGA | 23603 |
rs78620380 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CORO1C | GRCh38.p7 | 12:108700715 | TCACAAAAAAAGAGA[A/G]TATTATCTTACAAAT | 23603 |
rs78654370 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | CORO1C | GRCh38.p7 | 12:108668015 | ATTTTAGTCACCCAT[C/G]ATCAACTTGCTACTG | 23603 |
rs78677860 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108715444 | CAATGACAGAAATAT[A/G]TATTTCTATTACAGA | 23603 |
rs78791412 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108726669 | TAAAAAAAAAAAAAA[A/G]GAATGAAAAGAAAGT | 23603 |
rs78876552 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108683741 | TATAACTCTACCCAT[C/T]ACCACCTCCCAATCA | 23603 |
rs78894088 | snp | C/T | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108663673 | GTGGTTGCTTAGTGT[C/T]GGGGAGAGTGGAGGG | 23603 |
rs78980285 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108696352 | TTACCGATTCCTCCC[C/T]CTCTTACTTGTTTAA | 23603 |
rs79190880 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108677572 | ACTTTGGCATCTTAC[A/G]TCACTGTCTTGTACA | 23603 |
rs79245676 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108653475 | CAGCTTTACCACCCA[C/G]TGAAGGGCTATCTAA | 23603 |
rs79511784 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108650936 | CAACTAAAAAAAAAA[A/T]ATCACATAGAGAGTT | 23603 |
rs79522055 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108693867 | AAACCTGAATTCAAA[C/T]CGAACCTTCTCTGTG | 23603 |
rs79808687 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108648526 | TGGGACAGTACTCGC[A/C]GACGCCCTGGACCAC | 23603 |
rs79893389 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CORO1C | GRCh38.p7 | 12:108684208 | ATACTTCAATCTCAC[C/T]GATAATTAGAGAACT | 23603 |
rs79895816 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108684111 | CTAACAAAATCAACA[A/G]CCAAACAGAACGATG | 23603 |
rs80021046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108663909 | CTCACCACATCTTAA[C/T]TGGGGACATGCCTGG | 23603 |
rs80037164 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108702288 | TATTGTCGGGGGGAA[A/C]CAAAACCAGGCTGGG | 23603 |
rs80079174 | snp | A/C/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108694868 | TCACTCTGAATTACT[A/C/T]ATATATGAATTGTGT | 23603 |
rs80094928 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108698864 | GTGATCTTCCCTCTA[C/T]GCCACATTGACGCTA | 23603 |
rs80095558 | snp | A/T | 0.00858914 | 0.0649676 | intron-variant | CORO1C | GRCh38.p7 | 12:108654461 | TGTATACATTTTTTT[A/T]AAAATAAATTTTTAT | 23603 |
rs80217980 | snp | C/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108705513 | ACAGACAAGAAAGCC[C/T]AGACCCAGATGACTT | 23603 |
rs80228696 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108727559 | GGTCACCAGAGGATT[C/G/T]GAACAGGTGAATGGC | 23603 |
rs80288490 | snp | A/C/T | 9.91211e-05 | 0.00703923 | intron-variant | CORO1C | GRCh38.p7 | 12:108648922 | AATTTTATTTTTACA[A/C/T]TTGTTTAAAATATGG | 23603 |
rs80318260 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668324 | AGGGTTATAATATCC[G/T]CTGGCAAATGGCCCA | 23603 |
rs111412444 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108664008 | ACAACAAAGGTTTCA[A/G]AAGGTTAAGAAACAA | 23603 |
rs111415400 | snp | G/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108719373 | TACAAAATAATTCAT[G/T]TTTTGTGACCACTTA | 23603 |
rs111427069 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108675380 | AAGGACTCAGAAATC[C/T]TGAAGAGGTTTCAAT | 23603 |
rs111427394 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108653708 | AGTCTCCCTATAACT[A/G]TTATCACCCCTGAGC | 23603 |
rs111725371 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108698121 | GGCCAAGCCCTGCCA[C/T]AGCAGATCCTACTGA | 23603 |
rs111778831 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108721872 | AAACCAAGCCACTTC[A/G]CCAAAACCTAAGACC | 23603 |
rs111814471 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108706602 | AATATATAAAAATCA[C/T]TTTTTTTTTTAAGAT | 23603 |
rs111829744 | snp | G/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645804 | TGTGCAAGAATTCCC[G/T]TCGTGGTCCCAATGG | 23603 |
rs111861989 | snp | A/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108706601 | TAATATATAAAAATC[A/T]TTTTTTTTTTTAAGA | 23603 |
rs111873279 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659213 | CAATCAACCAAACAA[A/C]AACAAAGAACCACAC | 23603 |
rs111920971 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108674342 | TCGCGAGATCAGGAG[A/C]TGGAGACCATCCTGG | 23603 |
rs112041936 | snp | A/C | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108681388 | AGTATAAGTGAAAAC[A/C]AATTCTTATCTATTC | 23603 |
rs112044762 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731171 | TCCCCACAGGGACCC[C/T]GCTTCACGCTCCCCA | 23603 |
rs112093978 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108688446 | GCCATGTTCACCTTC[C/T]CAAACTCTCGAAATT | 23603 |
rs112293403 | snp | A/C | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108663239 | AAAATGGTATAGCCA[A/C]CATTTGGTGGCAGAC | 23603 |
rs112295412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700866 | TAAAATTCCTATGCC[C/T]GCCCATGCTCACAAC | 23603 |
rs112401537 | snp | C/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108711417 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23603 |
rs112468945 | in-del | -/ACA | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108666604 | TCCTGCAGCTCAGGG[-/ACA]ACAACAAACAGAAGC | 23603 |
rs112481456 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108652119 | AGTGATATCCTTAGA[A/G]AGTGCCATCTCATGG | 23603 |
rs113026497 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108678083 | TTTTGATTTAAGGGC[C/T]TCTTGAAAGGATTAT | 23603 |
rs113029519 | snp | A/G | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108679066 | CAGTGAGCCGAGATC[A/G]TGCCACTACACTCCA | 23603 |
rs113154234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108688035 | TACAGGCGATTCTCC[C/T]GCCTCAGCCTCCTGA | 23603 |
rs113167481 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108674291 | TTCTGGGCTGGGCAC[A/G]GTGGCTCACACCTTT | 23603 |
rs113199104 | in-del | -/CCTGGA | 0.49089 | 0.0668743 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703778 | GGCCTGACTATGGGC[-/CCTGGA]CTGGATGACACCCAG | 23603 |
rs113229040 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108688703 | TCTGAGGTCAGGAGT[A/T]CAAGACCAGCCTGGC | 23603 |
rs113567681 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731690 | CACGCCTCGCTACGC[C/T]CCCTCTGGTCGCACC | 23603 |
rs113599223 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108671229 | TGGTTGCAGCTACTC[A/G]GAAGGTTGAGGTGGG | 23603 |
rs113670826 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108673845 | TAACTAACCTGCACA[C/T]TGTGCACATGTACCC | 23603 |
rs113697866 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730485 | CCGGTGGGGACAGGC[A/G]GGAGAGCTCGGTTTC | 23603 |
rs113761563 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108717196 | TGAGTCCCAGCTGGG[A/T]GGAACAACAAAATAT | 23603 |
rs113869869 | in-del | -/AC | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108661843 | CGAAATGGCCTTGAA[-/AC]ACACACACGTGCACA | 23603 |
rs113904963 | snp | A/T | 0.5 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108665569 | GATACAGACAGTTAG[A/T]GAGTGAGCACCAGAG | 23603 |
rs114076659 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108722713 | GTCTTGAGTTGGGGA[A/C]CAAATGTACACACTG | 23603 |
rs114167500 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108729379 | TATTGTGTGCAGTTA[C/T]GTTTCATCGGTATGT | 23603 |
rs114176302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108690805 | TTAAAATAAAATTGA[A/G]CTAGAAAGCAAAAGC | 23603 |
rs114390574 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO1C | GRCh38.p7 | 12:108717066 | GGCAAGTGCTGGAAT[A/G]CAGAAGAACACAAGG | 23603 |
rs114394735 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108674867 | GTGAACACTGTTGAA[A/C]TGACAACAAAACATT | 23603 |
rs114458379 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | CORO1C | GRCh38.p7 | 12:108685126 | GTTGTTCTTAATTAC[A/T]TACTAAGAAGCTTCT | 23603 |
rs114563669 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CORO1C | GRCh38.p7 | 12:108712611 | AGTGGGAAATGTAAT[A/G]ATATATAAGCCTACA | 23603 |
rs114571565 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108670288 | CTGAGGGCAGCAGGC[C/T]GGTGTGAGATCAGCA | 23603 |
rs114585552 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108713727 | TGAACTACAAAGTAC[A/G]GAGCAGTTCCAACTT | 23603 |
rs114596728 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108686869 | CAAGCAACATGAGCC[A/G]AAAGGAAAATTCAGC | 23603 |
rs114626801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658037 | GTGGCAAATGAGGAC[C/T]TCTCAGACTTACTAT | 23603 |
rs114699236 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | CORO1C | GRCh38.p7 | 12:108695131 | TGCAGGATCTACTTT[A/C]AAGATGGCTCATCAC | 23603 |
rs114803880 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108676740 | TCACGCCATTATACT[C/T]CAACCTGGGTGACAA | 23603 |
rs114875164 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733248 | CAGTCCACGGCTCAC[G/T]GCAGCATGGACCTCC | 23603 |
rs114895749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726980 | GGGCAAAAGGGAGTT[A/G]CCCCATTCATGTTAT | 23603 |
rs114923629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691639 | TTCTCTGAGCCACCC[A/G]TGCAGCCAATCAAAG | 23603 |
rs114948398 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108725356 | ACAGACATTTAAGAG[A/T]GAAGAGAGGGAACAG | 23603 |
rs114951546 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CORO1C | GRCh38.p7 | 12:108684566 | AAAGTTTAAGGCACG[C/T]GAAATAAAAGTACAT | 23603 |
rs115017989 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | CORO1C | GRCh38.p7 | 12:108697996 | TAACATGGAAGATCA[A/T]TCTATTTTCTACCAG | 23603 |
rs115028537 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | CORO1C | GRCh38.p7 | 12:108709579 | ACTGTTCAGTTTTAA[A/C]CTTTAAATTAAGATG | 23603 |
rs115039223 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108729401 | TCGGTATGTATCTAT[A/T]AAAATTCATCAGGCT | 23603 |
rs115096497 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CORO1C | GRCh38.p7 | 12:108668369 | AAAATGGAATTAAGA[C/T]GAAGCCCTCCCTGCT | 23603 |
rs115217311 | snp | A/G | 0.0501905 | 0.150254 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731165 | GCCTCCTCCCCACAG[A/G]GACCCTGCTTCACGC | 23603 |
rs115220426 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108661555 | TTCCTTTTGTTTATA[C/T]ATGTTCTCTACAGTA | 23603 |
rs115372608 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108649150 | TCCCCACATCTGATC[C/T]ACCCCGGGAATAGGC | 23603 |
rs115373766 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108693327 | AAACAGAGACACTGT[C/T]CATGAAGGGGACTAT | 23603 |
rs115447459 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108716757 | GGATACAGTCCACAT[C/T]CCCCCCAGTAAAACA | 23603 |
rs115452546 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CORO1C | GRCh38.p7 | 12:108673018 | GGCCAATTAATAACC[C/T]TAAATGACCTTTAAG | 23603 |
rs115478623 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CORO1C | GRCh38.p7 | 12:108671164 | ATTGTGAGAAACCTC[A/G]TCTCTACAAAAAAAA | 23603 |
rs115515605 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108684678 | AGAATGGTATTCTAC[C/T]TGTATCTGTTATGCT | 23603 |
rs115608907 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108695377 | CAATATAGTAAGGCA[A/G]GTTTTTGGAGAACCT | 23603 |
rs115731161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108687291 | ACACTAAATTCAACA[A/T]AAATCTTAAGAAATC | 23603 |
rs115801712 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108670256 | GGGAAGGGACAGCAA[C/G]GGGACACCTGACAGA | 23603 |
rs115803861 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108713397 | AAAAAAATTCACATG[A/T]ATTACATAGCCTTCC | 23603 |
rs115855436 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | CORO1C | GRCh38.p7 | 12:108678713 | TAAAAGGATGTTCCA[C/T]GGCTTAAAAAAAAAA | 23603 |
rs115862808 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108699763 | TTTTTTGAACAGAAA[G/T]AAAAGTATCTAAATA | 23603 |
rs115879260 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | CORO1C | GRCh38.p7 | 12:108691095 | TATTACAACTTTTTT[G/T]GGGGGGTGGGAGGGG | 23603 |
rs116054557 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108709298 | TTAAGAGCCCAGTAA[C/T]AGCTTTTCCCTATCC | 23603 |
rs116212229 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730450 | AATCATTTGAGAGAC[C/G]GAGAGCTGGGGAGCG | 23603 |
rs116306658 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108725272 | GGAATCCATACCCTT[A/G]ATAGCTTAATGTCAG | 23603 |
rs116338080 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108721801 | GCTCTGGCCATTATA[A/T]GATGCCCCAATTTAC | 23603 |
rs116339430 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | CORO1C | GRCh38.p7 | 12:108709575 | AAAAACTGTTCAGTT[A/T]TAACCTTTAAATTAA | 23603 |
rs116395482 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108651496 | TCAAGCTAACCTACC[A/G]CCCCATTATAGGACC | 23603 |
rs116426326 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645825 | GTCCCAATGGCACTA[C/T]ACATTTCACGTTCAA | 23603 |
rs116495281 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108686094 | CCATACTAATAACGG[C/T]CTTATATGGTAAAGA | 23603 |
rs116613120 | snp | A/T | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658626 | TATTCACAGTTGGTG[A/T]CTACACACAACAGGG | 23603 |
rs116675127 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | CORO1C | GRCh38.p7 | 12:108691027 | GGTTTAATCCACAGG[C/T]CTCAGAATGAAAATC | 23603 |
rs116680636 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108682227 | AGCACAAAGATGGTG[A/G]AAATAAAACCAACTA | 23603 |
rs116735304 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108711985 | AAACCCCTACTAGTA[A/G]CAAAATCCTGCTCAG | 23603 |
rs116768161 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CORO1C | GRCh38.p7 | 12:108693837 | ATCTTTAGCTCCTAC[A/G]CAGAGGAAAAAAAAA | 23603 |
rs116796652 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108671171 | GAAACCTCGTCTCTA[C/T]AAAAAAAATAGAAAA | 23603 |
rs116799887 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | CORO1C | GRCh38.p7 | 12:108666964 | CCCTTAACAAAACTG[C/T]CACTCTCTGAGCCTG | 23603 |
rs116850923 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | CORO1C | GRCh38.p7 | 12:108682049 | TGTATAATTTCTGGG[G/T]GTGGGTGGGGGTGGA | 23603 |
rs116874279 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | CORO1C | GRCh38.p7 | 12:108650011 | GGAGTCCATTGAAGA[C/G]AACCTGGCAGATACA | 23603 |
rs116885977 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108675265 | TTCCGAAAGAAATGG[C/T]TTGGGCAGGGATGTC | 23603 |
rs117012226 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CORO1C | GRCh38.p7 | 12:108665848 | TAGTGGTGTGACCTT[A/G]AGGACATTCACCTAA | 23603 |
rs117025865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657806 | CTACCAATATCATAG[A/G]GCAGAAAGAAGCCTT | 23603 |
rs117058530 | snp | C/T | 5.00872e-05 | 0.00500411 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678367 | TGTGGCCACATACTG[C/T]AGGGTAAGATTTGTC | 23603 |
rs117132756 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108717769 | GTAAGGTATCTGAAA[A/G]GAGTAAAACCATGGG | 23603 |
rs117181453 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108709141 | TATATACTATAAACC[A/G]CTGAACTGTACACTT | 23603 |
rs117213531 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108724104 | TCCTAAAAACCTGGA[C/T]CAAACTTCACAGTTT | 23603 |
rs117286740 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108729996 | GAATGTAATCCCAGG[C/T]AGAAAGGCTGCGGTA | 23603 |
rs117295163 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CORO1C | GRCh38.p7 | 12:108663207 | TCAGAGCCTGCACAC[A/G]TGGCTGGTGAAAATG | 23603 |
rs117301595 | snp | A/G | 0.165527 | 0.235296 | intron-variant | CORO1C | GRCh38.p7 | 12:108654966 | CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 23603 |
rs117316420 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108667402 | TTTCTCAAAACTGTA[G/T]GCAGTGAGTGCAGAG | 23603 |
rs117333979 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CORO1C | GRCh38.p7 | 12:108665673 | AAAACATTAGTACCT[A/G]TGCCTGCGAGGTGTG | 23603 |
rs117383257 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108693869 | ACCTGAATTCAAACC[A/G]AACCTTCTCTGTGAT | 23603 |
rs117385557 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108678773 | CAAAATGTTAATACA[A/G]TAAGACAATATCCTC | 23603 |
rs117393101 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108672072 | CTGCCCAATCATTTT[A/T]TATTCAGAGAAACTC | 23603 |
rs117423030 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710385 | ATAAACTTGTTTTCA[C/G/T]TTTAAAAAGAAAAAA | 23603 |
rs117427136 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108697142 | TTGCAATAAGAAGCC[C/T]TATTTACTGCTGACA | 23603 |
rs117427270 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108662937 | ATACATTTGATAAGA[A/G]ACCCATAGCCTGAAT | 23603 |
rs117459536 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | CORO1C | GRCh38.p7 | 12:108692922 | CCTGTCTCAGCCTCC[C/G]GATTAGCTGCGATAA | 23603 |
rs117461253 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108662405 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 23603 |
rs117503985 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108647651 | AGTCACCAAGTTGAA[A/G]AGAGAAGTCAAAGCC | 23603 |
rs117508341 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108692003 | CCCACCCCACCCCTC[C/T]CAGCAAAACTGTGGA | 23603 |
rs117512837 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108725765 | TCCCGAAATGGCCAA[C/T]TGGTTTCTCCTAATT | 23603 |
rs117557461 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108707729 | AAACTTTTGCAAACT[G/T]TATATCTGATAAGAC | 23603 |
rs117615354 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108691105 | TTTTTTGGGGGGTGG[A/G]AGGGGCTAATGCCTT | 23603 |
rs117619728 | snp | A/C | 0.031825 | 0.122064 | intron-variant | CORO1C | GRCh38.p7 | 12:108663335 | ACTCCTAGGGATATA[A/C]CCAAGAGGATGGAAA | 23603 |
rs117660611 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108647749 | ACAGTGTGTCACAGT[A/G/T]TCACAGTGCCACTTC | 23603 |
rs117666396 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CORO1C | GRCh38.p7 | 12:108693393 | TCCATCAACGTGACA[A/G]AAGTCACTGCTTTTT | 23603 |
rs117746162 | snp | G/T | 0.039522 | 0.134904 | intron-variant | CORO1C | GRCh38.p7 | 12:108670816 | AAAAACTACATTATA[G/T]TGATTCAAAATAAGA | 23603 |
rs117852036 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108677476 | GTCCACTGGACAGAA[C/T]ACAGTTCTGCCATTA | 23603 |
rs117863216 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO1C | GRCh38.p7 | 12:108687094 | ACAGCCGAGTTCCTG[A/G]AGACTGATACTTCAA | 23603 |
rs117865607 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CORO1C | GRCh38.p7 | 12:108663336 | CTCCTAGGGATATAC[C/T]CAAGAGGATGGAAAC | 23603 |
rs118049100 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108688467 | TCTCGAAATTCAACA[C/T]TGGGAATTTTGCTTC | 23603 |
rs118065658 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645495 | CCTCAGCAGATTACA[C/T]TGATAAAGAAACAAA | 23603 |
rs118110680 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CORO1C | GRCh38.p7 | 12:108689624 | ACTGGTTACACCACC[C/T]GAAGATGTAAGGGCC | 23603 |
rs118170699 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108694573 | TCAATGTTAACATTG[A/C/T]ACATTATTTCCTAAA | 23603 |
rs137863327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108721850 | ATCAACTTTCCAAAG[A/G]TCACAGAAACCAAGC | 23603 |
rs137866444 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646371 | ACCCCTCTCCACATG[C/T]CCACATTTTTAGTCC | 23603 |
rs137918589 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108717707 | TTTGGTGTGGAGACT[G/T]ACTTACTACCTCTTA | 23603 |
rs137939419 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108650869 | CATATTTTGATTAGT[C/T]TGGTTTAAACCACAA | 23603 |
rs137970398 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108684376 | TTCAAGAGCAATTTG[G/T]TAACAGGTAGAGGTG | 23603 |
rs138072620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698045 | CAGCCAGCATCTCAG[A/G]TAGGAACAGCAACTT | 23603 |
rs138109873 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108689351 | AAGTAATAAATTCCC[A/C]TGGTGATAAAAAGTG | 23603 |
rs138112468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730164 | CCGGGGGAAATGAAC[A/G]ACTTGCAATTTGCTT | 23603 |
rs138119208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667414 | GTATGCAGTGAGTGC[A/T]GAGGAAAACAGACAC | 23603 |
rs138128974 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712571 | AAGCGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 23603 |
rs138132259 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108694209 | AGTGCTTGAACCTGG[A/G]AGGTGGAGGCTGCAG | 23603 |
rs138163879 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108687308 | AATCTTAAGAAATCC[A/G]GCGAAACCCTGTCCC | 23603 |
rs138235183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708044 | TGGGAATGCAAAATG[C/T]TGCAGCTGATGTGGA | 23603 |
rs138250407 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672877 | ACTGCACTCATATAA[C/G]ACAGTGAACTTCATC | 23603 |
rs138291345 | snp | C/G | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662067 | GCCGTTGGATGCCAA[C/G]CCACGATGCCGACTC | 23603 |
rs138366985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108670897 | GTGACAGACATCAAG[A/G]AAAAAATTAGAAATA | 23603 |
rs138394832 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CORO1C | GRCh38.p7 | 12:108680584 | AATTACTCCATCCCT[C/T]AACCTCGGTTCCTCA | 23603 |
rs138432039 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108698654 | TCAGGTGATCCGCCC[C/G]CCTCAGCCTCCCAAA | 23603 |
rs138436436 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645828 | CCAATGGCACTACAC[A/G]TTTCACGTTCAATCA | 23603 |
rs138446179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108716401 | TTTATTAATAACTTC[A/G]TAAGGCTAGTCACAG | 23603 |
rs138492992 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108714241 | TAAAAATACAAAAAT[C/T]AGCAGGGCGTGGTGG | 23603 |
rs138494724 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO1C | GRCh38.p7 | 12:108705399 | TGGGAGGCAGAGGTC[A/G]CAGTGAGCCGAGATC | 23603 |
rs138535236 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108726358 | TGGGAGGCAGAGCTT[A/G]CAGTGAGCTGAGATC | 23603 |
rs138669139 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CORO1C | GRCh38.p7 | 12:108694033 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCACTT | 23603 |
rs138683527 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704060 | TTTCCTCTTCACTCA[A/G]ATAGGCCAGATACCA | 23603 |
rs138711508 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108676047 | AGGAGGAATCTTTAG[A/C]TTAAGACTTAAAAGA | 23603 |
rs138711843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108721154 | TAGAAATCACTAACA[C/T]TAGTGACACCCACAA | 23603 |
rs138746213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651578 | TGGTTCTTCCACTCA[C/T]AGGGTAGGAAAACCA | 23603 |
rs138767522 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108717444 | ATTTTAAAAGCTCAC[G/T]CTGAATGAAGCTGGA | 23603 |
rs138774818 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108722748 | CCTCCAAAACAGAAA[C/T]TTCATCTGGGCTCTT | 23603 |
rs138785128 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646670 | AGAAAGGAAAAGAAG[A/G]AATACGACGTGAGCT | 23603 |
rs138791979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659882 | GTAATCAAGTAGCTA[C/T]ATAGATTCAGAAACG | 23603 |
rs138831397 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108710071 | ATACAAACCTTACTT[-/G]GTCTTTTTAAGATGT | 23603 |
rs138858188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660210 | TAATCCCAGCACCCT[A/G]GGAGGCCGAGGCGGG | 23603 |
rs138860147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108709927 | GATCATCTCAGTAAT[A/G]AAGAGGAAGACGATG | 23603 |
rs139003471 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108672165 | TTCCCACTCCTTCTT[A/G]AGGAATCCACCCAAG | 23603 |
rs139027441 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732434 | TGAAAGTCGGAGCAC[A/G]GGAATTTGAGCCTCA | 23603 |
rs139037336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667658 | GAAGTGAGGCTCGGC[A/G]TTCAAGGCCAGCCTG | 23603 |
rs139088712 | in-del | -/ATA | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108715319 | GAACTAAAAGATGCC[-/ATA]ATGAGGCCTGTAACT | 23603 |
rs139146685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710885 | TTCTTACATGTTGGG[C/T]GAATATTTTAACCAA | 23603 |
rs139157556 | snp | A/C | 3.39899e-05 | 0.00412235 | intron-variant | CORO1C | GRCh38.p7 | 12:108647550 | AAAAAGGAGGCAGTG[A/C]TTAAAATGCAGTAAA | 23603 |
rs139158619 | snp | A/C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108723218 | TAACAGAGATGACAG[A/C/T]GCACTTTCACGTGTG | 23603 |
rs139212404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679650 | CAGGCTTCTTAGCAA[C/T]TTTTCAAGAACAGAA | 23603 |
rs139319796 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108678046 | GAAAAAGAAAGACAC[A/G]GCAGACACTGCAGTA | 23603 |
rs139320231 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108727648 | CCTTTCCCCAGTCCT[C/T]TCACATTTGGGTTTC | 23603 |
rs139334112 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660472 | AAAAAAAAAAAAAAA[-/AA]GAAGTAGGAAACTGG | 23603 |
rs139386424 | snp | C/T | 0.000197674 | 0.00993972 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648607 | CACTGGTCCTCACCA[C/T]ACTGGCCGTGTCTGT | 23603 |
rs139403513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108677220 | AAGTACTCCCATTTG[C/T]GTTTATGCCTAACCT | 23603 |
rs139429006 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732512 | TTTGGGCCTGAGTCC[C/G]CTAATCTTCAGCATG | 23603 |
rs139481559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108673991 | TACTGCATGGTTTAC[C/T]GAATATTTTAAGCCC | 23603 |
rs139517774 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703875 | CCTCCTGGCTCCCAA[A/G]ATACCACCTGCCTTA | 23603 |
rs139529616 | snp | A/G | 0.000214177 | 0.0103461 | intron-variant | CORO1C | GRCh38.p7 | 12:108701109 | TCTACCAGAATGGAA[A/G]ATCAAATTACCTACC | 23603 |
rs139566146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108674322 | GGGAGGCCAAGGCGG[A/G]CGGATCGCGAGATCA | 23603 |
rs139582152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687760 | AGTGTACTCCAGCCT[A/G]GGTGACAGCGAGACT | 23603 |
rs139589616 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657057 | TAAAATTAAAAAAAA[-/A]TTAAAAAAATAAAAA | 23603 |
rs139621669 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678018 | CTCCATCTCAAAAAA[-/A]AAAAAAGAAAAAGAA | 23603 |
rs139703627 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108652902 | AAACTCAGTTTTAGT[A/G]AGTATCCTCAGAAAG | 23603 |
rs139714990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696570 | TGCCAACGTGGTAGA[C/T]TACACAGAGGGCTGA | 23603 |
rs139820945 | snp | G/T | 0.0154263 | 0.0864636 | intron-variant | CORO1C | GRCh38.p7 | 12:108648578 | GCCTGAACCAGCCAA[G/T]CACCCCTGCACTCCA | 23603 |
rs139821097 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108694917 | ACGTAATACAGTCTA[A/C]GAATATATGTATTAG | 23603 |
rs139887547 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CORO1C | GRCh38.p7 | 12:108692086 | GTAATGAGGCCAGGC[C/T]GTGCTCGTGTGGCTG | 23603 |
rs139916586 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108718092 | GGCCTGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 23603 |
rs139922883 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108714838 | CAAAGAAGAGCACTC[A/G]TATATTTACATTTTA | 23603 |
rs139979598 | in-del | -/AGTT | 0.231482 | 0.249313 | intron-variant | CORO1C | GRCh38.p7 | 12:108665563 | TGGTGTGATACAGAC[-/AGTT]TAGAGAGTGAGCACC | 23603 |
rs140020741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108652635 | CATGCCTTTTAAGTG[A/G]TCTCCTCAGCCTCCT | 23603 |
rs140023717 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695900 | AAATGATTTTCTGTA[G/T]AGCTAAATTCTTTCA | 23603 |
rs140092308 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108718763 | ATCTTCTAAAGCGAA[A/G]GAAAAAACAAAACAA | 23603 |
rs140099949 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108655433 | CTCTCCCTCTGATGC[C/T]GAGCCGAAGCTGGAC | 23603 |
rs140104353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661818 | AGCTTTCCTCAGGTT[A/G]TCGAAATGGCCTTGA | 23603 |
rs140131149 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732697 | TTTTTTATTTTAAGC[A/G]TCAGCCTCAGAAACG | 23603 |
rs140137076 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108656677 | AGAAGGAAGTAGACA[C/T]GGGAGACTTCATTTT | 23603 |
rs140231517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654871 | CCACCACCCGTGGCT[A/T]ATTTTTGTATTTTTA | 23603 |
rs140239359 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108729105 | CGTCGACATACCCAC[C/T]TATATAACTAAGAAT | 23603 |
rs140248379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668737 | CAATTATGCAATCCC[A/G]TTGTCCAAATTAGCC | 23603 |
rs140250129 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714367 | GCACTCCTCCAGCCT[A/G]CAGCCTGGCAACAGA | 23603 |
rs140261481 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648987 | AACAGTCATAATAAT[A/G]GGTTCACACTTTCTC | 23603 |
rs140304744 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108693088 | CAAGCTTGAGCCACC[A/G]CGCCCGGCTAAACCA | 23603 |
rs140314066 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108710712 | GGGACAACAGGTGTG[C/T]GCCACCACACCCTGC | 23603 |
rs140369934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697576 | AGTTGCCAAGACACT[A/G]AAGTTGTAGGAGTCT | 23603 |
rs140444818 | snp | C/G/T | 0.00172157 | 0.0292889 | intron-variant | CORO1C | GRCh38.p7 | 12:108678443 | TATCAACACCACAGA[C/G/T]GTTATACATTTTCTC | 23603 |
rs140445519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108672938 | ACCACCTGCTCTTCC[C/T]GTATTCCTGTCTCTT | 23603 |
rs140451273 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108719490 | AGTTGTAGTGGTGCA[A/C]AATTCACCCTATCTT | 23603 |
rs140504503 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | CORO1C | GRCh38.p7 | 12:108706747 | CTACACTGCACCCAG[C/T]TAATTTTTGTATTTT | 23603 |
rs140514721 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108666714 | CAGAGCTGGGACACT[A/G]ATTGGTCATGTTAGC | 23603 |
rs140559060 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108650004 | CTGGGCAGGAGTCCA[C/T]TGAAGACAACCTGGC | 23603 |
rs140582947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711326 | AGTGGGCCATGATCA[A/T]GCCACTGCACTCCAG | 23603 |
rs140719474 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108728064 | AACAAGTGTTGGCAA[C/G]AATGTGGAGAATTTA | 23603 |
rs140759292 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108728750 | TTCTATTACTTAACA[C/T]TCTAGGTACTAGGTC | 23603 |
rs140800408 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108651114 | CCACGACCACACATA[A/G]CAAATTTTTTATTTT | 23603 |
rs140814696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693918 | GCCTAGGGTGAAACT[A/C]TCTCTCACACCCCAG | 23603 |
rs140851075 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108691332 | AGGAGCAGATGATTT[G/T]CTACATGTGGTTATA | 23603 |
rs140899112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659395 | AACTTTGATTTTCCC[C/T]TGCTATACAATTAGT | 23603 |
rs140931985 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108654637 | TGACAACATAATGCG[C/G/T]GCATACATCAGCGTG | 23603 |
rs140946141 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683481 | AATAACAAAATCAAC[C/T]AAACTGGATAGATCA | 23603 |
rs140975501 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703187 | AGCTGCAATCCCTAC[A/C]AGCATCTTCAAGCAA | 23603 |
rs141048623 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108688914 | ACATGCCTGTAATCC[C/T]GGCTACTCGGGAGGG | 23603 |
rs141053860 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108724938 | TAGAGGCTCTTTTCC[C/T]ACACAGGATGTTACA | 23603 |
rs141143640 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108717473 | GAGAATGGATCTGCA[A/C/T]GTGGGAGCATCTGAA | 23603 |
rs141208210 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108715242 | GTGTCTCTTAAAAAA[A/G]CAAAACAAAACAAAA | 23603 |
rs141208304 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108670929 | ATGAAGACAAACCAA[A/G]AAAGAACACAAGAGC | 23603 |
rs141220526 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108712239 | AAATATCCTAAACTC[A/T]GTTATTTAAATGACA | 23603 |
rs141249388 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646718 | CCATGAAATGAGAGC[A/G]GTGGTAATATGAATC | 23603 |
rs141267749 | in-del | -/AAAT | 0.163892 | 0.234703 | intron-variant | CORO1C | GRCh38.p7 | 12:108673893 | TAATAATAAAATAAA[-/AAAT]AAATAAATAAATAAT | 23603 |
rs141288767 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108691010 | CATTGCAGCTCTGCA[C/T]TGGTTTAATCCACAG | 23603 |
rs141302762 | snp | C/T | 0.000595031 | 0.0172384 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662046 | GCACTAAGAAGCACA[C/T]TGCGGGCCGTTGGAT | 23603 |
rs141312714 | snp | A/G | 0.175897 | 0.238765 | intron-variant | CORO1C | GRCh38.p7 | 12:108674527 | CGCTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 23603 |
rs141333840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108664685 | GCCTCTTTCCCCTGC[A/G]GAGAACATGGGCATC | 23603 |
rs141476620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669429 | AACAGTCCATTATAC[A/G]TTTACAGCTTCCTTT | 23603 |
rs141513033 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108712988 | ATTTTCTAAATTAAA[C/T]CCAGCAGTGACACTC | 23603 |
rs141558483 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108699948 | AAATCAGATGTTATA[A/G]TAAAACAAGTTAGTC | 23603 |
rs141560385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108672396 | TTTCAACTAAAAGTC[A/G]TTTAGTTTTTTAACG | 23603 |
rs141599477 | in-del | -/A | 0.031825 | 0.122064 | intron-variant | CORO1C | GRCh38.p7 | 12:108647599 | AAACTTGTAAGATAT[-/A]AAAATGTAGTTTTCT | 23603 |
rs141619729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108680465 | GTGTCACAGGAAGGA[A/G]CCACACAGTTCATTT | 23603 |
rs141653743 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108722113 | CCTTGCTGTAATGAC[C/T]GAATGCAAACATTTC | 23603 |
rs141736646 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108652529 | GACCCCGCTTCAGTA[A/G]CTGACCTTTTCTTCC | 23603 |
rs141740083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684146 | AATTACACAAGCAGA[C/G]AACTCACAGCGAAGA | 23603 |
rs141752010 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108679766 | ATAAGACAGGTAAGG[A/G]TTCAAATCCAGGCTC | 23603 |
rs141754823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727285 | CAGGGACAAATGTCT[A/G]CCTGTGAGATGAGGA | 23603 |
rs141821039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726548 | GGCATGGTGCATCAC[A/G]CCTATAATCCTAGCA | 23603 |
rs141864153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694959 | TGATTAACAAGTTAT[C/G]CTAAAATTCAGCTGA | 23603 |
rs141941845 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | CORO1C | GRCh38.p7 | 12:108675805 | ATCATGTGCTTCCTA[A/G]CGTATGGAAGAACAT | 23603 |
rs141977748 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108663999 | TAACAATGAACAACA[A/C]AGGTTTCAAAAGGTT | 23603 |
rs142077812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696986 | CTGCTTGCTGCATAT[A/G]TGTGTGTCTTTGTAT | 23603 |
rs142089556 | in-del | -/GAAACAAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679130 | AAAAAAAAAAAAAAA[-/GAAACAAG]AAAAAAGAAAAAAAA | 23603 |
rs142092657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705896 | CTCAGACACAGAAAA[A/G]GCATTTGAGGCTGGG | 23603 |
rs142127988 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108667976 | TTTATTTTTCAAATA[C/T]TGCTTTCCAGACACT | 23603 |
rs142159844 | snp | A/G/T | 0.00104616 | 0.0228515 | intron-variant | CORO1C | GRCh38.p7 | 12:108702769 | TAAATGCAGAGAGAC[A/G/T]AATTTATTTTTGCCA | 23603 |
rs142171866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698256 | TACTTGCCAAAGTTA[C/T]ACATTGAATTAGGGG | 23603 |
rs142364373 | snp | C/G | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646459 | GCAGTACACGTCTTC[C/G]TGTCCTGGGCACCCT | 23603 |
rs142392542 | snp | C/G/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108649852 | CGGCTGGTGTGCAAG[C/G/T]GGGGAGTTGAATGTG | 23603 |
rs142408726 | in-del | -/AG | 0.19334 | 0.243495 | intron-variant | CORO1C | GRCh38.p7 | 12:108685671 | GGCCATCAGAAACAC[-/AG]AGTTAATAAAAAATG | 23603 |
rs142425853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108692963 | CCACCATGCCCAGCT[A/C]ATTTTTGTATTTTTA | 23603 |
rs142531143 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108720196 | GTCTCAAACACTCAT[A/G]CAGACACACACACAC | 23603 |
rs142532889 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645140 | TTTTATCTCTGAAAA[C/T]GGAAGCAAGTGTTTT | 23603 |
rs142542965 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108716541 | ACATGTACTCCTGAC[A/G]GTGTTTCAAAGGAAC | 23603 |
rs142544277 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108687409 | GGAGGATCACCTGAG[C/T]CCAGGAGGTCAAGGC | 23603 |
rs142546420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108668346 | AATGGCCCAGATGCA[A/G]TCTGTACAAAATGGA | 23603 |
rs142647034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108674023 | CCATTGAGAACCACC[A/G]ATCAGGAAAAAAAAA | 23603 |
rs142662192 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108649764 | CAAGACGGGAAACAA[C/T]AAAAAAAGTCTCTAA | 23603 |
rs142691160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108673698 | GTGACTTTAAGTTGA[C/T]GCCAATGCTCATTTA | 23603 |
rs142710311 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | CORO1C | GRCh38.p7 | 12:108714720 | GTAAGCCAAGATCAC[A/G]ACACTGCACTCCAGC | 23603 |
rs142724229 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714511 | ATTACAGGTGCGGTG[A/G]TTCACACCTGTATTC | 23603 |
rs142738064 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108676730 | TGAGCTGAGATCACG[A/C]CATTATACTCCAACC | 23603 |
rs142742201 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712914 | GATCATGTCTCTTTA[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs142764814 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108667550 | CATTTTCTGTTTGGA[C/T]AACACATTACTATGG | 23603 |
rs142810789 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660037 | AGGATGTTAGTTCAA[A/G]GATGAAGCAAAATAC | 23603 |
rs142840382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723858 | TGCCAATTTTTCTGG[C/T]AAGATGCAATGCAAG | 23603 |
rs142863747 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CORO1C | GRCh38.p7 | 12:108714556 | GGCTGAGCTCAGGAG[C/T]TGGAGACCAGCCTGG | 23603 |
rs142938342 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108728492 | TGGGGTTTCTTTTTG[C/G]GGGGGATGAAAATGT | 23603 |
rs143023335 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108709358 | ATTATGGGCTAAAAG[G/T]AGAATTTTCATATAA | 23603 |
rs143023503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661346 | CATTAAAAATAGGAA[A/G]AGAGCTTAATGGCAC | 23603 |
rs143087404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684454 | AGATGCTCCCATATT[C/T]TGTACAAGAGGAATA | 23603 |
rs143115944 | snp | A/G | 0.000296492 | 0.012172 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658818 | TCAGACTGCCATTCC[A/G]GTTCCAGCTCACATT | 23603 |
rs143148641 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731693 | GCCTCGCTACGCCCC[C/G]TCTGGTCGCACCGAG | 23603 |
rs143225890 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733530 | CACTAGTTAATAAAT[G/T]AAACAGGGGCATTGA | 23603 |
rs143266205 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108706686 | TGCAACCTCCGCCTC[C/T]GGGGTTCAAGCGATT | 23603 |
rs143396538 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CORO1C | GRCh38.p7 | 12:108710622 | CAGGCTGGAGTGCAG[C/T]GGCACAATCTCGGCT | 23603 |
rs143419159 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108718118 | CAGTACTTTGGGAGG[C/T]CAAGGCGGGCAGATC | 23603 |
rs143467241 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658658 | CCCACTGACCAGTAC[C/T]GCTGCCTGCCTTAAA | 23603 |
rs143487064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108714250 | AAAAATTAGCAGGGC[A/G]TGGTGGCGCACAACT | 23603 |
rs143501666 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108721447 | TCACAGTCTATACTG[C/T]AGAATTCACCATCAA | 23603 |
rs143509755 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646065 | GGAGGGACATGTTTG[C/T]ATGCATTAAAGCTAC | 23603 |
rs143564799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694159 | TGATGGTACACACCC[A/G]TAGTCCCAGCTACTC | 23603 |
rs143573451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665674 | AAACATTAGTACCTA[C/T]GCCTGCGAGGTGTGC | 23603 |
rs143683564 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108670674 | AATTAAATCCACATA[A/C]AAATAAGCAAGAAAA | 23603 |
rs143793342 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108675709 | AGAATTTACTGTCAC[A/C]ATATTGCAACCCCTA | 23603 |
rs143816150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727650 | TTTCCCCAGTCCTCT[C/T]ACATTTGGGTTTCAA | 23603 |
rs143820214 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108652739 | TGCCAAACAGCTACA[C/T]TGCAATTCAACTGTG | 23603 |
rs143827636 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108716161 | AAAAAAAAAAAAATC[A/C]TTGAATATGTTTCTA | 23603 |
rs143847683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661845 | TTGAAACACACACAC[A/G]TGCACACACACACAA | 23603 |
rs143862037 | snp | C/G/T | 0.000166446 | 0.00912125 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678278 | GGAGCTTACCATGAC[C/G/T]GTGCAGTCCTCTGAA | 23603 |
rs143897619 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732126 | CTCAACGTTTAAACC[C/T]CAAGCCCCGCCCCGA | 23603 |
rs143899708 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | CORO1C | GRCh38.p7 | 12:108655837 | CATCTCTGCCTGGCC[A/G]CCCATCGTCTGGGAT | 23603 |
rs143950407 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672893 | ACAGTGAACTTCATC[A/G]ATAAACGCTGTGTGT | 23603 |
rs143963240 | snp | C/T | | | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701124 | GATCAAATTACCTAC[C/T]TTGTGCAGAGGGAGG | 23603 |
rs144022280 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108696818 | TGGGAATCACGTGTG[C/T]TAATCTAAATCAACC | 23603 |
rs144130421 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108677792 | GGGAGGCCGAGGCAG[A/G]CGGATCACTTGAGGT | 23603 |
rs144144633 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108718054 | GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAT | 23603 |
rs144190846 | in-del | -/AAAATAAATAAC/AAAATAAGTAAC | 0.561924 | 0.150458 | intron-variant | CORO1C | GRCh38.p7 | 12:108683459 | GAAGTCAGTGGAAAA[-/AAAATAAATAAC/AAAATAAGTAAC]AAAATAAATAACAAA | 23603 |
rs144241661 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108715139 | TTTGGGAGGCTGAAG[C/T]AGGAAGATCCCTTGA | 23603 |
rs144249408 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108699567 | CTGTCTTCTCAGTTG[A/C/G]CTGCCATAAAGCCTA | 23603 |
rs144253059 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CORO1C | GRCh38.p7 | 12:108669182 | AACTGCAAAGTAGCT[A/G]TCACTAAATCAATGC | 23603 |
rs144298863 | in-del | -/A | 0.219049 | 0.248077 | intron-variant | CORO1C | GRCh38.p7 | 12:108661596 | ATTGTATAGCAGGGG[-/A]AAAATCAAAGTTTTC | 23603 |
rs144323376 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732658 | ACTTCCCAAAGCAAG[C/G]CATCTTTGCCATTCA | 23603 |
rs144387439 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | CORO1C | GRCh38.p7 | 12:108656372 | CCAGCCGCCCCGTCC[A/G]GGAGGGAGGTGGGGG | 23603 |
rs144473799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664226 | AAATTTAAGAACTTG[G/T]CAATGAAAAATCATG | 23603 |
rs144475640 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108710830 | GCCTTCCAAAATGCT[A/G]GGATTACAGGTGTGA | 23603 |
rs144490525 | snp | A/G | 0.000798881 | 0.01997 | intron-variant | CORO1C | GRCh38.p7 | 12:108710325 | GGAGGATTACGGGCT[A/G]CTCTGCCTATGGAGT | 23603 |
rs144518110 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648734 | GCCTGGAATGTACCC[A/G]TGCTTCAAGGAGATG | 23603 |
rs144540123 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108706242 | ATTAAATACTCTTTC[A/G]TGATAAAACACTCAA | 23603 |
rs144602398 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108714530 | ACACCTGTATTCCCA[A/G]CACTTTGGGAGGCTG | 23603 |
rs144623415 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108652483 | GGATTATGGGGGTGT[A/C]TCTCTCCTCTACAAA | 23603 |
rs144623802 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | CORO1C | GRCh38.p7 | 12:108726171 | TTTAAAAATAAACAT[A/C]ATCTGGGAGGCCGAG | 23603 |
rs144627823 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108651352 | TGAGTCTCAGAGGAT[A/T]TATTTGTTGACTAGC | 23603 |
rs144694685 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108654848 | CTGGGATTATAGATA[A/G]GCACATGCCACCACC | 23603 |
rs144696817 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108728871 | TAATTCAAGGAGACA[A/G]TAACACAGAGAAGTC | 23603 |
rs144698349 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CORO1C | GRCh38.p7 | 12:108660758 | GGAATTCCAGCTCTG[C/G]AATTTTTTTCCTCTC | 23603 |
rs144737336 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108723300 | TCAATTCTTTAAGTT[A/C]CTAAGAATGAAAGGA | 23603 |
rs144800601 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO1C | GRCh38.p7 | 12:108668265 | GTGCAGAGTGGCACC[A/G]AGTTCGGGAAAACCA | 23603 |
rs144875917 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108683747 | TCTACCCATCACCAC[A/C]TCCCAATCAATCAAT | 23603 |
rs144878552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663608 | TTGCAGGATTCCATG[C/T]ATGTGAAATGTCCAG | 23603 |
rs144887994 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108728113 | GGTGAATACCGTAAA[A/G]TGGTGCAGCTGCTTT | 23603 |
rs144950906 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108724999 | TCAAGCACTGCAGTG[A/C]AATCTCCTTCAAATC | 23603 |
rs144967609 | snp | A/G | 8.24844e-05 | 0.00642148 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654353 | GGTCATAGAAAGGCA[A/G]CAACACCCCATTGCT | 23603 |
rs144973798 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108725874 | GGAGTGCAACTCTGT[A/C]GCCCAGGCTGGAGTG | 23603 |
rs144981859 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108670168 | AAACTAGGTGATATC[C/T]CCAAAATTTAAGCAG | 23603 |
rs145019721 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108671822 | GGCTGTAGTACAGTG[A/G]CACGATCACGGCTCA | 23603 |
rs145065768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108674839 | GATGGAATGTACTCC[C/T]GGTAACGACGCTGTG | 23603 |
rs145270979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702634 | CAACTCAGCTGAAAA[A/T]CAGATCCTCATATAC | 23603 |
rs145282594 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689186 | GCCTGGGCAACAGAG[A/C/T]GAGACTCCATCTCTG | 23603 |
rs145325902 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652342 | CTCTCTGAGGCTCCT[G/T]GCTGCTGAATGTGTT | 23603 |
rs145373401 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108693569 | AAAGGGTCAAGAAAT[G/T]TAGGATTTTCTACCA | 23603 |
rs145400562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678849 | TGTAAAGGCCGGGCG[C/T]GGTGGCTCACGCCTA | 23603 |
rs145441429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108701707 | CAAAGTGAAATTCTC[C/T]GGTAGAGGTGAGGCT | 23603 |
rs145537977 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108689010 | CACTCCAGCCTGGGC[A/G]ACAGAATGAGACTCT | 23603 |
rs145548307 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108706628 | AAGATGGAGTCTTGC[C/T]CTGTCACCCAGGGTG | 23603 |
rs145564427 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108726563 | GCCTATAATCCTAGC[A/G]CTTTCGGAGGCTAAG | 23603 |
rs145618573 | snp | A/C | 0.00716266 | 0.059414 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644745 | ACAGTAGCGGCCATG[A/C]AGCGAGGGTTGTTTG | 23603 |
rs145652289 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108707526 | AGAGCTAAAACTATA[A/C]AACTCTGAGAAGAAA | 23603 |
rs145683753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688841 | TCGAGACCAGCCTGG[A/C]CAAAATGGTGAAATC | 23603 |
rs145706944 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | CORO1C | GRCh38.p7 | 12:108711453 | GGGAGGCCAAGACAA[A/G]TGGATCGCCTGAGGT | 23603 |
rs145732864 | in-del | -/A | 0.163892 | 0.234703 | intron-variant | CORO1C | GRCh38.p7 | 12:108691201 | CCAGAAATGAAACCC[-/A]AGTCACCGTTCCTCC | 23603 |
rs145748526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108711161 | AGAGTCCAGGAGTTC[A/G]AGACCAGCCCAGGCA | 23603 |
rs145870283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108717191 | AAAAGTGAGTCCCAG[A/C]TGGGAGGAACAACAA | 23603 |
rs145963955 | snp | C/T | 0.000362629 | 0.0134604 | intron-variant | CORO1C | GRCh38.p7 | 12:108701073 | CTATTAAGGAAAAAG[C/T]ATGGAGACTATCAGA | 23603 |
rs146016806 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646638 | ATTCTGGTACAAACA[C/T]CCAATTTCTAGAAAA | 23603 |
rs146021826 | snp | A/G | 0.192088 | 0.2432 | intron-variant | CORO1C | GRCh38.p7 | 12:108655695 | TGCTCAATGTTGCCC[A/G]GGCTGGAGTGCAGTG | 23603 |
rs146022156 | snp | C/T | 0.000733138 | 0.0191319 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702826 | GTGAAAGTGGCCTCT[C/T]TCCAATGCTGGGGGC | 23603 |
rs146043359 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674572 | AAAAAAAAAAAAAAA[-/A]CCTTCTGGAAAGGAT | 23603 |
rs146112964 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108705816 | ATGCGAGGTTGGGTC[A/G]ACATCTGAAAATCAA | 23603 |
rs146151542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667655 | AAGGAAGTGAGGCTC[A/G]GCGTTCAAGGCCAGC | 23603 |
rs146155338 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108661461 | TTATGTATGTGCACA[A/G]AAATATCTTTCGGAA | 23603 |
rs146207533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659515 | TTGATGTTTCTTTCC[A/G]AAAGATATTTCTGTG | 23603 |
rs146232868 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO1C | GRCh38.p7 | 12:108723104 | TTGCTTGCCAAGAAA[A/G]ACTAGGATGACATTG | 23603 |
rs146272178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108687261 | TGACTTAGCAAAAAA[C/T]ATTCCTCTTTAGGCA | 23603 |
rs146275653 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108680671 | ATGAGACAATCAAGG[A/T]AAAGAACTTGGTTCT | 23603 |
rs146330498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108682441 | AAATGCACTATTAGC[A/G]ATTAATGTCACTATC | 23603 |
rs146341234 | in-del | -/CCATTGTGATGAGATGTA | 0.0637235 | 0.166737 | intron-variant | CORO1C | GRCh38.p7 | 12:108700108 | TCAGAATCACATGAT[-/CCATTGTGATGAGATGTA]CCCTGAATATAAGGG | 23603 |
rs146393781 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704797 | TAGCAATTAAGAGAG[C/T]AAACTCCAGAGTCAG | 23603 |
rs146396594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108700513 | AAGTTGAAGAAAACA[C/T]AGAACCATTCTCAGT | 23603 |
rs146413332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693724 | TCCTGGAGTCTGAAG[A/G]AGGAATGTGCCTACC | 23603 |
rs146451272 | snp | A/G | 0.00158345 | 0.028093 | intron-variant | CORO1C | GRCh38.p7 | 12:108654271 | AATGTTTCCACTTAC[A/G]GGATTTAACACCAAA | 23603 |
rs146455303 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108696855 | AGGACTGAGGACTTT[C/G]TATATTCCTCCGGCA | 23603 |
rs146468367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660180 | AAACTGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 23603 |
rs146534590 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108711666 | GCTTGAGTGACAGAG[C/T]AAAACTCCGTCTCAA | 23603 |
rs146572610 | snp | A/G | 0.164873 | 0.23506 | intron-variant | CORO1C | GRCh38.p7 | 12:108674434 | ATGACTGTAGTCCCA[A/G]CTACTCGGAGGGCTG | 23603 |
rs146590694 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108715187 | TGCACTGAGCTATTA[C/T]TGCACCACTGAACTT | 23603 |
rs146651186 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108729053 | TGACAAATCAAAATA[C/T]GAGAAATTAAAATTT | 23603 |
rs146653832 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108655003 | GGCCACTGCGCCTAC[A/C]CTATTTTATTTTTTT | 23603 |
rs146716909 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108677944 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTAC | 23603 |
rs146773146 | in-del | -/GG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662477 | TCCCAAGTATCGGCT[-/GG]GTTTTTAAAATGTAA | 23603 |
rs146775962 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108675230 | AATAGATATAATTTT[C/T]CCTTAAAATAAACCA | 23603 |
rs146817658 | snp | A/C/T | 4.95514e-05 | 0.00497732 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678318 | ATGACCTGATCGTTA[A/C/T]GTGGGCACCAGTCTA | 23603 |
rs146846953 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108676036 | GAAAATGATGAAGGA[A/G]GAATCTTTAGATTAA | 23603 |
rs146910738 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108679329 | ATTAGCCAGTTCCAC[A/G]TCTGATTAAGAATAA | 23603 |
rs146956059 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108680278 | TTTCTTCTGGGAAAG[G/T]TAAGTTCTAAGTTGA | 23603 |
rs147020690 | snp | A/G | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662050 | TAAGAAGCACATTGC[A/G]GGCCGTTGGATGCCA | 23603 |
rs147061311 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CORO1C | GRCh38.p7 | 12:108698309 | TTTCTTTGCTGAATT[C/T]TGAGTACACACCAAC | 23603 |
rs147132916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710685 | TCTCCTGCCTCAGCC[G/T]CCCGAGTAGCTGGGA | 23603 |
rs147235538 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108727670 | TTGGGTTTCAACTTA[C/T]ATAACCAAAATATTG | 23603 |
rs147253163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108652877 | AAAAAGTGAGATTTT[C/T]CTAATGAAGAAACTC | 23603 |
rs147275685 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732342 | GACCCCATTTCGCAG[A/G]TGAGGGAATGGAAAC | 23603 |
rs147276847 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108655959 | TGCCCGGCCGCCCAT[C/T]GTCTGAGATGTGGGG | 23603 |
rs147380492 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108676837 | CTTAACAAAATGCGT[A/C]CATAGCCATTAAAAT | 23603 |
rs147449734 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108691753 | TCAGGCCTGCGGGCC[A/G]GCTGCTGTGGACATA | 23603 |
rs147470153 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694277 | ACAGAGCAAGACTGT[C/T]TCAAAAAAAAAAAAA | 23603 |
rs147482343 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108652530 | ACCCCGCTTCAGTAG[A/C]TGACCTTTTCTTCCT | 23603 |
rs147485504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694897 | GTGAACTAACATTAT[A/G]AGTCACGTAATACAG | 23603 |
rs147485862 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108648321 | GAGGCTCCTGTTCAC[A/T]CTGAGAGATAGGAGG | 23603 |
rs147637287 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108706111 | AGAATTGCTTGAACC[C/T]GGGAGATAGCAGTTG | 23603 |
rs147653636 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108702720 | GCTAATTCCTTTCCT[C/T]TAATTCCCTTCCTCA | 23603 |
rs147739062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724725 | AAGAAATGTAGATCA[G/T]TGCCTGACCAAAGGG | 23603 |
rs147742517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649710 | AATGACTTCTCTTAT[C/G]ATGACCCTGATAAGG | 23603 |
rs147745941 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644997 | CCCTGTACTTACCCC[C/T]GGAGAGGAGTATGGC | 23603 |
rs147758015 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108719893 | ACTCTAAAGTCAAAC[G/T]TGCTAACCAGGCCAG | 23603 |
rs147848608 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669258 | ATTTATACCATAAGT[A/G]ATACAAAAAGCAGTT | 23603 |
rs147851282 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108664682 | CAGGCCTCTTTCCCC[G/T]GCGGAGAACATGGGC | 23603 |
rs147918310 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108725562 | GTGAAGCCCAGCTCT[A/G]TCTGGCCCTAAAGGC | 23603 |
rs147952217 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108688725 | CAGCCTGGCCAACAC[A/G]GTGAAACTTCATCTC | 23603 |
rs147968320 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108728247 | ACAGCATTATTCATA[A/G]TAGCCAAAAAGGAAA | 23603 |
rs147968731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684016 | AAAGCAAACCAAATT[C/G]AGCAGTGTGAGTTGT | 23603 |
rs148017712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680296 | AGTTCTAAGTTGAGG[C/T]CTGAATATGGCCCTG | 23603 |
rs148022617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652489 | TGGGGGTGTCTCTCT[C/G]CTCTACAAACCCAGC | 23603 |
rs148023136 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726771 | AAATACTATCAGGGT[C/T]GGCCTGTATGCATTT | 23603 |
rs148179707 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108675743 | AATGACTGGATATAG[A/G]CACAGAATACACAAA | 23603 |
rs148182762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108684464 | ATATTTTGTACAAGA[A/G]GAATATTTATTGCCG | 23603 |
rs148236548 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108689878 | GCAAGGAGAATGTTA[A/G]GTCACACATGTGCTC | 23603 |
rs148246664 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658834 | GTTCCAGCTCACATT[A/G]TAAATCATGTCTGAA | 23603 |
rs148250061 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731939 | CCTCTGAGCCCCGCG[C/T]ACTGCCTATCCGAGT | 23603 |
rs148304931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699817 | AAAAGATTCATCTTC[A/G]CCAATAAGAAGGTAC | 23603 |
rs148321362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666170 | GAATATCCAGTCTCA[A/C]AATAAAACACGCAGA | 23603 |
rs148387076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108712541 | ATTGTGCCACTACAC[C/T]CCAGCCTGAACAACA | 23603 |
rs148438196 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108710526 | CTAATATTCATAATA[C/T]TTAACATCTAAGGAA | 23603 |
rs148505203 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108723475 | ATCAAAAGTAGAAAA[C/T]ACAGCCTGACGGCTT | 23603 |
rs148548510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108653513 | AGGGACTACCTCAAC[A/G]GCTCCACTGTTATTA | 23603 |
rs148565900 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108668301 | CGAGTGTTGGGTTCC[A/G]ATCTGCCAGGGTTAT | 23603 |
rs148645441 | in-del | -/AGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705592 | ATTTTCCAAAGATAG[-/AGA]AGAAGGGAACACTTT | 23603 |
rs148699633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677848 | ACATGGTGAAACCTC[A/G]TCTCTATTAAAAATA | 23603 |
rs148774211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108705854 | AACACATTATATCAA[C/T]AGAAGAAAAAAAAAT | 23603 |
rs148823100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658619 | CTTCTCTTATTCACA[A/G]TTGGTGTCTACACAC | 23603 |
rs148826176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108701855 | TCTATTCCCCAGAGT[A/G]TTTCAACAAGAATAG | 23603 |
rs148840681 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108721167 | CACTAGTGACACCCA[A/C]AAATTACACTTTCAC | 23603 |
rs148857954 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646005 | GCCTCTGTGCTTTGA[C/T]GCAGCCTTGGTGAGA | 23603 |
rs148879698 | snp | C/T | 0.162581 | 0.234218 | intron-variant | CORO1C | GRCh38.p7 | 12:108706647 | TCACCCAGGGTGGAG[C/T]GCAGTGGTGCAATCT | 23603 |
rs148931796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675695 | GAAAACAAAATGACA[G/T]AATTTACTGTCACCA | 23603 |
rs148999882 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108716102 | CCACTGCACTCCAGC[C/T]TGGCAATAGAACGAG | 23603 |
rs149021672 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662317 | GACCGTGTTAGGCGG[-/T]TTTTTTTTTTGTTTG | 23603 |
rs149027703 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108726068 | TCAAACCCCTGACCT[C/T]GTGATCTGCCCGCCT | 23603 |
rs149030026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696934 | ACACCTCATAAACCA[C/T]ATGCTTAAAATAAGC | 23603 |
rs149051449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684434 | CTAGGTGGTCTGGGT[A/G]AGAGAGATGCTCCCA | 23603 |
rs149062887 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658801 | TTTGGAAGCTGTGCA[A/G]ATCAGACTGCCATTC | 23603 |
rs149079477 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731482 | CGCTGCAAAGCCGGG[A/C]GAAGCCTCCAACCGC | 23603 |
rs149087806 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108670187 | AAATTTAAGCAGGTG[A/G]GAGCAAACACCAACA | 23603 |
rs149226774 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | CORO1C | GRCh38.p7 | 12:108678972 | AAAAATTAGCTGGTC[A/C/G]TGGTGGTGTGCGCCT | 23603 |
rs149292814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694080 | GAGGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 23603 |
rs149348526 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108660659 | CATTCTCCTTCACAT[C/G]TAAAAGGGAGAATGC | 23603 |
rs149364457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723229 | ACAGCGCACTTTCAC[A/G]TGTGTTCCTCAGTCC | 23603 |
rs149371960 | in-del | -/AA | 0.0501905 | 0.150254 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645526 | TACAGATTTGAATAT[-/AA]GTCATTGCCATTATT | 23603 |
rs149378019 | snp | C/T | 1.64985e-05 | 0.0028721 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701319 | TACCACTCGCCTCAT[C/T]GTGTCTGCAAAGGAA | 23603 |
rs149416305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710104 | TTTATCACTCTCCTC[C/T]TATTTTCCAATACAA | 23603 |
rs149469292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108677759 | CACTCACAGAAAAGA[C/T]TGTAATCCCAGCACT | 23603 |
rs149507463 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108655670 | TGCAAACGGAGTCTC[A/G]TTCACTCAGTGCTCA | 23603 |
rs149525241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717874 | TTATGTACTTTTGCT[C/T]GCAAAAGTGTCTGGA | 23603 |
rs149615566 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108672892 | GACAGTGAACTTCAT[C/T]GATAAACGCTGTGTG | 23603 |
rs149698104 | snp | A/G | 0.000181221 | 0.00951722 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701277 | TTTCACCGCTTGCCC[A/G]AATACATGCCGAAAC | 23603 |
rs149780966 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108715466 | TATTACAGAGATAAT[A/G]TGCAAGGATGACATG | 23603 |
rs149788602 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108647620 | GTAGTTTTCTATTTT[A/G]CAAACGGCAAGCCAT | 23603 |
rs149819630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695925 | CTTTCATAAAACCCT[A/C]CATGAAAAACTGCAA | 23603 |
rs149842601 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108652908 | AGTTTTAGTGAGTAT[C/G]CTCAGAAAGTGCCAT | 23603 |
rs149872202 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108663022 | GGCCAGTCATCTAAA[C/T]AGACATTTCAAGGAA | 23603 |
rs149925886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670083 | TGGGGGTTTTTCCGA[A/C]GTCCCTCCGTAAAAA | 23603 |
rs149942616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108711160 | TAGAGTCCAGGAGTT[C/T]GAGACCAGCCCAGGC | 23603 |
rs150001378 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108688135 | AGGCTGGTCTCAAAC[A/T]CCTGACCTCAGGTGA | 23603 |
rs150049934 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108719558 | AATTCTCAAATACAT[G/T]AAATCCTTGGGGCTC | 23603 |
rs150051153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692399 | TTGTCTAAAACAGAG[C/T]ACCACAATGTGTAGA | 23603 |
rs150065926 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732655 | TTTACTTCCCAAAGC[A/C]AGGCATCTTTGCCAT | 23603 |
rs150155334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693960 | TTCATGCACAAAGCA[C/T]CCCCCTGGAGAGATC | 23603 |
rs150223631 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703481 | CAAATGTGACAATAA[A/G]CTTTCGAAGATGGAA | 23603 |
rs150313626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108650209 | TTTTTTTTTTTTTGG[C/G]ACTGGGTCTTGCTCC | 23603 |
rs150321606 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108725662 | ATAGCTCACTGTCCC[C/T]AACTAGACAAAAAAG | 23603 |
rs150363868 | snp | A/G | 0.1652 | 0.235179 | intron-variant | CORO1C | GRCh38.p7 | 12:108655439 | CTCTGATGCCGAGCC[A/G]AAGCTGGACGCTGCC | 23603 |
rs150380191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108697892 | CTGTAAAATGTATAA[C/T]CATTATTCAAATATT | 23603 |
rs150413643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678803 | CCAATATATAAATTA[C/T]CAGTTCTGGAAATGA | 23603 |
rs150432779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667349 | GTTAGCTTTTCTTTG[G/T]TCTATGGCTACAGAC | 23603 |
rs150487345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108672476 | CTATTACATGTATAA[C/T]GTGAAAAGACAAATG | 23603 |
rs150516974 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108680482 | CACACAGTTCATTTA[C/T]AGGCAGCGAAGTATA | 23603 |
rs150525554 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | CORO1C | GRCh38.p7 | 12:108688448 | CATGTTCACCTTCCC[-/A]AACTCTCGAAATTCA | 23603 |
rs150538704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668630 | AAGGGAGAAGCGTCC[G/T]TTAAACTTAAAAATT | 23603 |
rs150552662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108714739 | CTGCACTCCAGCCTG[A/G]GGGACACAGTGATAC | 23603 |
rs150570500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687757 | GCCAGTGTACTCCAG[C/G]CTGGGTGACAGCGAG | 23603 |
rs150637843 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108691042 | TCTCAGAATGAAAAT[C/T]CACCCTCCTTGGATG | 23603 |
rs150690616 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108695580 | CCAATGGATGAGTTC[C/T]TCTGTTTCAGTAAAT | 23603 |
rs150742562 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108661888 | GCTGGGGGAGCAGTG[C/T]ACCCCAATACTCTTC | 23603 |
rs150745751 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CORO1C | GRCh38.p7 | 12:108705924 | GGGCATGGTGGCTCA[G/T]GCCTGTAATCCCAAC | 23603 |
rs150778526 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647226 | TTGTTTCTGCAAATT[C/T]GGGAGACAAATTGAG | 23603 |
rs150899262 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732494 | GGACAGTTCTCTTAC[C/G]TCTTTGGGCCTGAGT | 23603 |
rs150904635 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | CORO1C | GRCh38.p7 | 12:108656304 | GGGGGCTCAGCCCCC[A/G]CCCGGCCAGCCGCCC | 23603 |
rs150953637 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108728739 | ACCCAGAGAGATTCT[A/G]TTACTTAACATTCTA | 23603 |
rs151005576 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659084 | AGAGGCCCTACCAGA[A/G]GCCCTACTTACTAAC | 23603 |
rs151010482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674121 | TACAAGGAGATTAAC[A/G]TTGTTTTCACCTGCT | 23603 |
rs151029853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683356 | CCTGAGAGGCAGAGG[C/T]TGCAGTGAGCTGAGA | 23603 |
rs151080296 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108688849 | AGCCTGGCCAAAATG[C/G]TGAAATCTCGTCTCT | 23603 |
rs151165613 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108693050 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGCGCT | 23603 |
rs151215787 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108697330 | ACCAGAAACAAAAAA[C/G]GGAAAACATTCTCAG | 23603 |
rs151223348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108710853 | AGGTGTGAGCCACCG[C/T]GCCTGGCCTAAAATT | 23603 |
rs151239276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719467 | CTAAGCGATTAGATC[A/G]TTTTAACAGTTGTAG | 23603 |
rs151287196 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | CORO1C | GRCh38.p7 | 12:108706746 | ACTACACTGCACCCA[A/G]CTAATTTTTGTATTT | 23603 |
rs151306281 | snp | A/C | 4.98161e-05 | 0.00499055 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647513 | TCTCATCCAACTTGG[A/C]TTCATTTTGCTAAGA | 23603 |
rs180753234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671993 | GTCTTGAACTCCTGG[G/T]CTCAACCCGTCCACC | 23603 |
rs180766585 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646413 | CTCAAGAGCTGGGCA[A/G]GCTGCTGAAAAGGGC | 23603 |
rs180972792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685082 | AAACACAAAGCAATT[C/T]TGAGGGGAATCTGGA | 23603 |
rs180991787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695703 | TCTCTTCCTCAACCA[A/G]CATGACAGAAACATT | 23603 |
rs180997447 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708005 | TGAGAATATAGACAA[A/G]TCAGAACCCTCATAC | 23603 |
rs180999041 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731733 | CGGTGCCCAAGCGCA[C/G]GCCCCGCTCTCCAGT | 23603 |
rs181014491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108718939 | ATTCAATTTCACCAA[C/T]AAAATGAAAATATCT | 23603 |
rs181249011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664267 | GAACACGTGAGAAAA[A/G]GAATTTTCCTTTGTG | 23603 |
rs181274249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713713 | AGATGCAGTGACCTT[G/T]AACTACAAAGTACGG | 23603 |
rs181284407 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108671119 | GGGAGGAATGCTTGA[A/G]GCCACAAGTTAGAGG | 23603 |
rs181295487 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645439 | ACTTCATTAATTCGA[C/T]ATCAGAACCTTAAAA | 23603 |
rs181309465 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706457 | AGAAAAAGGAGTAAG[A/G]GACATTCAGATTGGA | 23603 |
rs181320508 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659468 | AATCACTTTTAATCC[C/T]ACCACTCAGAGAGAA | 23603 |
rs181399824 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108684293 | AAAAGTATAAATATA[A/G]GTGCTGACAAGGATG | 23603 |
rs181435978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108653120 | AAAATAGCTAGGTGG[C/T]ATCATGCCTCAACAG | 23603 |
rs181453025 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731226 | CCCTTTCCCCGAGCC[C/G]CCGACAGCAGCCCCC | 23603 |
rs181563624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108689292 | TCGCACAACGCTTTA[C/G]CCAGCAGGCCTACTC | 23603 |
rs181624133 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108701928 | CAAAAGCCTTCTAAT[C/T]TCCTTCTAACACAGA | 23603 |
rs181628591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724420 | GGCAGTTAAGTTCCT[A/G]ATCTTGGGTAAATCT | 23603 |
rs181631210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677906 | TGCCTGTAATCCCAA[A/T]TACTCGGGAGGCTGA | 23603 |
rs181694730 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713246 | TTTGTATTCCACTGC[C/T]GATATGGACTTGTTG | 23603 |
rs181699722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663873 | AGAAAATCCTCTTGA[C/G]TAGTGAAGACATGCA | 23603 |
rs181824716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658323 | AGTGCTGGGATTACA[A/C]GTGTGAGCCACCATG | 23603 |
rs181836765 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CORO1C | GRCh38.p7 | 12:108705431 | CGCCACTGCACTCCA[A/G]CCTAGGTGACAGAGC | 23603 |
rs181843253 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647028 | AAGCAATGTGGCATT[A/G]GTCCCTATTCATTAA | 23603 |
rs181848236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683281 | AAACTTAGCCAGGCA[G/T]GGTGGTGGGTGCCTG | 23603 |
rs181887884 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652494 | GTGTCTCTCTCCTCT[A/G]CAAACCCAGCAGTAG | 23603 |
rs181907276 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108677610 | CCAGCAGTTTCAGTT[C/T]TTTCTCTCCTTTTGG | 23603 |
rs181976535 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714165 | GGAGGCCGAGGTGGG[C/T]GGATCACGAAGTCAA | 23603 |
rs182051698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672813 | TGTATCTGTTACAGT[C/G]ATCAGTAATGTCTGA | 23603 |
rs182082701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719961 | AGGCTGAGGCGAGAG[A/G]ATCACTTGAGCCCAA | 23603 |
rs182161309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108666040 | CCGACCGCACTACTA[C/T]GAAATTAGCTTCCTG | 23603 |
rs182169056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108700907 | TAATTTTTTCATCCA[C/T]AGAGGGCATCCCCAG | 23603 |
rs182375111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714696 | TGAGCCCAGGAGGCA[A/G]AGGTTGCAGTAAGCC | 23603 |
rs182379974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692660 | CAAGGCATGGTATAG[A/C]CCAAGTACTTTCCAA | 23603 |
rs182382735 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108667048 | ACTAAATATTATCAT[G/T]CACATAAAGGCTTAG | 23603 |
rs182389613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696569 | ATGCCAACGTGGTAG[A/C]TTACACAGAGGGCTG | 23603 |
rs182403800 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108659896 | ACATAGATTCAGAAA[C/T]GGATTCTGAAAGAAG | 23603 |
rs182427211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108723604 | GAGACATGGGGACCC[A/C]CACCCAGTTCCACAA | 23603 |
rs182455844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691253 | ATCACATGCCCTCTC[A/G]GCTCATTCTTCCCCA | 23603 |
rs182548158 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647333 | CGCCCTCCCTAGGAC[C/G]ACACCAATAACCAGC | 23603 |
rs182576919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696979 | AAGTGTGCTGCTTGC[A/T]GCATATGTGTGTGTC | 23603 |
rs182580005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720125 | TGGGAGGGCGACGCT[A/G]CATTGAGCCTCAATC | 23603 |
rs182591198 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673517 | CTGGATAAGATCATT[A/G]ATGAAGGTGGCTACA | 23603 |
rs182672976 | snp | A/G | 0.00299761 | 0.0385981 | intron-variant | CORO1C | GRCh38.p7 | 12:108648873 | AGACATTTGGCACCC[A/G]TGGGTAAGGAAGAAG | 23603 |
rs182696888 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698204 | GCTGGGCTCAGCTTT[A/G]CCTTAGTGAAAAAGC | 23603 |
rs182788868 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725590 | GGCCTGCACCCTCAC[A/C/G]GCCTCAGTTCCCCTA | 23603 |
rs182990951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674320 | TTGGGAGGCCAAGGC[A/G]GGCGGATCGCGAGAT | 23603 |
rs182992734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678490 | TATTACCTCCACCCA[A/G]AACTCTCAATTTTCT | 23603 |
rs183016934 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720737 | ACCATGTTAGCCAGG[A/C]TGGTCTCGACATCCT | 23603 |
rs183055686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661329 | ATGGATTAGTATGAA[G/T]TCATTAAAAATAGGA | 23603 |
rs183100267 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108710402 | TTAAAAAGAAAAAAA[A/T]TGGATTACGGGACAG | 23603 |
rs183145202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680882 | GCATCCTTGAGTTAC[C/T]ACCCCAGGTAATATT | 23603 |
rs183170991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726850 | GTGCGCCAGTCATTA[C/G]TGTTCATCGGGGGAA | 23603 |
rs183180160 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704266 | ATCACGAGGTCAGGC[A/G]ATCAAGATCATCCTG | 23603 |
rs183208017 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732712 | GTCAGCCTCAGAAAC[A/G]TGTGTTATTTAAATC | 23603 |
rs183215142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698693 | ATTACAGGCATGGGC[C/T]ACTGTGCCCGGCCAG | 23603 |
rs183226342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649445 | GCCAGCTTGAGGTGG[C/T]TGAACATATAAGTAT | 23603 |
rs183228820 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108709032 | ACTGCTTGGATTATA[A/G]GCATTAGCCACCATG | 23603 |
rs183262931 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702849 | CTGGGGGCATGTAGC[C/T]GGGCTGAAGTAAGAG | 23603 |
rs183271844 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108654712 | TTCTTTTTCTTTTTT[C/T]TTTTTTTAAAGACTG | 23603 |
rs183366040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108687522 | AGGTGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 23603 |
rs183440249 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704112 | AGATTAATATAAATA[C/T]GTAAAATGCTTTGTC | 23603 |
rs183444837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108680396 | AAAACGCATCACCAA[A/G]AAAGGACTTCAAAAA | 23603 |
rs183447834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108655038 | TACTTCTTTAATTAT[A/G]AAATATGTGTGCTTT | 23603 |
rs183544918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705366 | TAGGGAGGCTGAGGC[A/G]TAAGAATTGCTTGAA | 23603 |
rs183547614 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729964 | GAGTGACTAAGAGCC[C/T]TACAAGTACTGTTTT | 23603 |
rs183567319 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108682369 | GCAAATAAAGGAGGG[C/T]GGCATATTAAAAAGT | 23603 |
rs183580012 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108656572 | CAGCTCATTGAGAAC[A/G]GGCCATGATGACGAT | 23603 |
rs183587045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691921 | TCAAAAATAGCCCCG[G/T]GGTACATTGGGAAGT | 23603 |
rs183674630 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108721458 | ACTGCAGAATTCACC[A/G]TCAAAGAGTCATGTG | 23603 |
rs183737673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661583 | GTATACATGTACTAA[C/T]TGTATAGCAGGGGAA | 23603 |
rs183756124 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108711715 | ATCTTATAAGCTACA[C/T]AGGAAACATGTAGGG | 23603 |
rs183769596 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108666347 | AAAAAGTCTCTGAAA[C/T]GAAATAAGAAGACAA | 23603 |
rs183795127 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714322 | TGAACCCGGGAGGCA[A/G]ATGTTGCAGTGAGCC | 23603 |
rs183844219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108685760 | ACAGAGAAAGTAGTA[C/T]TCTACTGTAGCACAA | 23603 |
rs183964686 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | CORO1C | GRCh38.p7 | 12:108715650 | CTCCCCCCCTCCCCC[C/G]CGCATACTCACAACA | 23603 |
rs184000829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695109 | CACCTGATGGCTTTA[C/T]TAGGGCTGCAGGATC | 23603 |
rs184005781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671308 | CCAGCCTGGGTGACA[A/G]AGCAAGACCTTGTCT | 23603 |
rs184008121 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645936 | AAGTTCCAGCTAACC[A/G]AGGAATGAACAGGTG | 23603 |
rs184030824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660823 | AATGATTCCCAAGTA[C/T]AGTCGATGGTGATTA | 23603 |
rs184040679 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108718110 | TGTAATCCCAGTACT[C/T]TGGGAGGCCAAGGCG | 23603 |
rs184153456 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726298 | GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTTGG | 23603 |
rs184256907 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108675201 | ATATATATACATAAT[A/G]CTACTGCATACTTAA | 23603 |
rs184351988 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730707 | CCTCCCAACCCCCAG[C/G]CAGTCCCAGCCCTCT | 23603 |
rs184452016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663913 | CCACATCTTAATTGG[A/G]GACATGCCTGGGCAC | 23603 |
rs184454333 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108699456 | AAAAAAAAAGTCTTA[C/G]ATTTATCCCTCAGTC | 23603 |
rs184459159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108722049 | GACTAGCCTCCTTAC[A/G]TGGGGTCTGCCTGAC | 23603 |
rs184500872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706118 | CTTGAACCCGGGAGA[C/T]AGCAGTTGCAGTAAG | 23603 |
rs184507174 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108651637 | TCCCTACTTGCCCAC[C/T]AGGGAACGCTGACCA | 23603 |
rs184575470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728115 | TGAATACCGTAAAAT[A/G]GTGCAGCTGCTTTGG | 23603 |
rs184593235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681637 | ATGACAAGAAAAAAG[C/T]AAACAAAAGGCACTG | 23603 |
rs184635371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108676671 | CAGCTACTCGGGAGG[C/T]TGAGGCAGGAGAATC | 23603 |
rs184658423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722897 | CATAAAAAGATCAAA[C/T]TAGCAGTCTTAGGGA | 23603 |
rs184693664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670197 | AGGTGGGAGCAAACA[C/T]CAACAGCCACACGAC | 23603 |
rs184694750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | CORO1C | GRCh38.p7 | 12:108657557 | GGAGGTCAGTGTTAA[C/T]CATCCCCCTTCCCCA | 23603 |
rs184698150 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644998 | CCTGTACTTACCCCC[A/G]GAGAGGAGTATGGCA | 23603 |
rs184729111 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704700 | CCAAGGTCAAATCTG[A/G]TCTGGGCTCACCTGT | 23603 |
rs184768951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657992 | AGATGCAGCCAAAGA[A/G]CAACCACATCTCAGG | 23603 |
rs184977832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108650310 | CAGCCTCTGGAATAA[C/T]TGGGACCACAGGTAC | 23603 |
rs185112548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713418 | ATAGCCTTCCAAATA[C/G]TTTCATCCCATCATT | 23603 |
rs185196216 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108690434 | GTCTTTTTGGACAGA[A/G]GTGAAAATGCCAAGC | 23603 |
rs185241754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685106 | ATCTGGAAGTACTAG[C/G]ACTAGTTGTTCTTAA | 23603 |
rs185255575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660538 | GCTAAACTCTGGGAT[A/G]GACAATTGAACCTTC | 23603 |
rs185278940 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108708007 | AGAATATAGACAAAT[C/T]AGAACCCTCATACAC | 23603 |
rs185284963 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731907 | CCCCAGAGCCCCTCA[A/G]TACAGGAACATTAGC | 23603 |
rs185318072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694362 | AATGAATATGTGAAT[C/G]AATGAATGTGATTTT | 23603 |
rs185325556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713773 | GTCATACTTTTCCAA[A/C]AATCAATCCCGAATC | 23603 |
rs185351281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697432 | TATCAACATGTATTG[A/G]AGCCTAACACACATC | 23603 |
rs185351992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720254 | ATAAAATACAGCCAT[A/G]AGAAACCCATGCTGC | 23603 |