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 |