SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs701378 | snp | C/T | 0.441977 | 0.16014 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122860 | CAGTTCTGAAGTCTG[C/T]GTCCCTCCATAAGGG | 7464 |
rs701379 | snp | A/T | 0.439085 | 0.163545 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124543 | TAATAACAGAATTCA[A/T]CAGAAGGCATCATCT | 7464 |
rs715910 | snp | C/T | 0.399611 | 0.200291 | intron-variant | CORO2A | GRCh38.p7 | 9:98149229 | aacaacaaatCGTTA[C/T]TTTTGCTTTTTTCtt | 7464 |
rs735111 | snp | A/G | 0.173399 | 0.23798 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133161 | AAGCCCCATGAGTAC[A/G]ATTAGCTGTCACCAA | 7464 |
rs751800 | snp | A/C | 0.235273 | 0.249566 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122282 | GTGGAGCTTATATGA[A/C]CATACAGGCCCTACT | 7464 |
rs753991 | snp | C/G | 0.0759472 | 0.179459 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123010 | GCAAACCCAGATCAC[C/G]CCACAGGTAGTTTTC | 7464 |
rs774121 | snp | C/T | 0.40263 | 0.198 | intron-variant | CORO2A | GRCh38.p7 | 9:98143706 | ACCATTACCCAGTTT[C/T]ATTGTTGCTCAGTAT | 7464 |
rs774122 | snp | A/G | 0.3746 | 0.216737 | intron-variant | CORO2A | GRCh38.p7 | 9:98149448 | gaatatgtgaggctg[A/G]gtatttacaaagaaa | 7464 |
rs774123 | snp | A/T | 0.398534 | 0.201091 | intron-variant | CORO2A | GRCh38.p7 | 9:98149568 | atcatgcagacagtg[A/T]aggggggatcaggtg | 7464 |
rs774124 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190931 | CCATGGCCGCAGGGC[A/G]AGGTCATAGGCACTA | 7464 |
rs812280 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98154329 | cttatgtgTTTGTGt[A/G]tatatatatatatat | 7464 |
rs814027 | snp | C/T | 0.444 | 0.157683 | intron-variant | CORO2A | GRCh38.p7 | 9:98149389 | ATGAGAAGCTCTGAT[C/T]AGTGGCTCCTGGGtg | 7464 |
rs882265 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98157761 | TTGAACTGACCACTG[C/T]CCTGCTCGTACCCTC | 7464 |
rs942164 | snp | C/T | 0.0551013 | 0.156571 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122752 | CCTGGGGGACTCTTC[C/T]GTTAACTAGGGCTGA | 7464 |
rs942165 | snp | G/T | 0.2768 | 0.248559 | intron-variant | CORO2A | GRCh38.p7 | 9:98127058 | TGTAGGAACAGCACG[G/T]TGCGTGCACTGAAGC | 7464 |
rs1063628 | snp | A/C | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121238 | CTTTGGCAGGTATCC[A/C]CCTTAACGCTACAAT | 7464 |
rs1201535 | snp | G/T | 0.4021 | 0.198407 | intron-variant | CORO2A | GRCh38.p7 | 9:98143774 | ACAAACTGTTCTGCA[G/T]GGGGACTCCCATCCT | 7464 |
rs1539288 | snp | C/G | 0.492918 | 0.0590819 | intron-variant | CORO2A | GRCh38.p7 | 9:98168803 | AGCATGAAGCAGCCT[C/G]CCAGGGGCCAAGTGG | 7464 |
rs1539289 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | CORO2A | GRCh38.p7 | 9:98168831 | TGGCTCGTGAGAGTT[C/T]CAACCCCTGGTGCAA | 7464 |
rs1539290 | snp | A/G | 0.167158 | 0.235875 | intron-variant | CORO2A | GRCh38.p7 | 9:98168876 | GAAACAGACACACAC[A/G]TGCAGAAGGCTAGCT | 7464 |
rs1544204 | snp | C/G | 0.287085 | 0.247234 | intron-variant | CORO2A | GRCh38.p7 | 9:98160405 | AGACCTCAGATTTGG[C/G]TCTGAGCTTCCTAGT | 7464 |
rs1544205 | snp | A/G | 0.259674 | 0.249813 | intron-variant | CORO2A | GRCh38.p7 | 9:98160592 | AAATGACCTCCCTAG[A/G]GTCTTGGCAACTTGG | 7464 |
rs1746239 | snp | C/T | 0.455181 | 0.142831 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123497 | CTATTCTCTCTCTCt[C/T]ttttttttttttttt | 7464 |
rs1891322 | snp | C/T | 0.449091 | 0.151204 | | | GRCh38.p7 | 9:98160338 | AGAGATCACCTGAAA[C/T]GCAGGAGGAGTTAAG | 7464 |
rs1891323 | snp | A/G | 0.0554779 | 0.157039 | | | GRCh38.p7 | 9:98122656 | CTACTTCTTTACCTC[A/G]TATAGTCATTTCAGA | 7464 |
rs1977261 | snp | A/G | 0.49168 | 0.063958 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174098 | ggcaacgagagtgaa[A/G]ctctgtTCCCCCGCC | 7464 |
rs1983815 | snp | A/C | 0.312104 | 0.242163 | intron-variant | CORO2A | GRCh38.p7 | 9:98175828 | aatggggatgataac[A/C]ataaatgagttaata | 7464 |
rs1985859 | snp | C/T | 0.440195 | 0.162252 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173831 | TAAGAGCGTGTAGCC[C/T]TTGGTCTGGGTGTGG | 7464 |
rs2050982 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98140710 | ttgccctcctaaagt[G/T]agggattacaggcat | 7464 |
rs2050983 | snp | G/T | 0.370974 | 0.218781 | intron-variant | CORO2A | GRCh38.p7 | 9:98140965 | aacattaaacttata[G/T]aagttgataatgtac | 7464 |
rs2093697 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157097 | TAGCTAGTTTTGACT[A/C]AATGTTTGTTTCCCT | 7464 |
rs2181580 | snp | C/T | 0.452473 | 0.146644 | intron-variant | CORO2A | GRCh38.p7 | 9:98167052 | GAGGCTGCAGTAAGC[C/T]ATGATTATACCACTG | 7464 |
rs2181581 | snp | C/T | 0.466824 | 0.124448 | intron-variant | CORO2A | GRCh38.p7 | 9:98187927 | AGTTTCAATAAGCCA[C/T]GTAACTTTTCTGTAT | 7464 |
rs2231652 | snp | C/G | 0.249603 | 0.25 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173472 | AGTGCTCATGGAGCC[C/G]GTGGATTTTGGACAG | 7464 |
rs2231653 | snp | C/T | 0.117537 | 0.212022 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173391 | CTCTGCAGAGTGCCC[C/T]GGCCACACTCACGAA | 7464 |
rs2231654 | snp | A/G | 0.0733688 | 0.176922 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173244 | GGCTTCCTAGTCACC[A/G]GGAACTTGGTGGAAG | 7464 |
rs2231655 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173185 | ccgaatcagaaactc[C/T]agggtggggcccaac | 7464 |
rs2231656 | snp | C/T | 0.144632 | 0.226711 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172939 | CATGTAAATGTGATG[C/T]TGTCACCTGTCCTCA | 7464 |
rs2231657 | snp | A/G/T | 0.0821764 | 0.185298 | intron-variant | CORO2A | GRCh38.p7 | 9:98157777 | TGCATCACCGTCCAC[A/G/T]TTGAACTGACCACTG | 7464 |
rs2231658 | snp | A/C/G | 0.000148251 | 0.00860852 | missense | CORO2A | GRCh38.p7 | 9:98137652 | TACCCAAAAGTCTGC[A/C/G]GGCACAGAGGCAACG | 7464 |
rs2231659 | snp | C/G/T | 0.00271441 | 0.0367402 | missense, synonymous-codon | CORO2A | GRCh38.p7 | 9:98137647 | AAAAGTCTGCGGGCA[C/G/T]AGAGGCAACGTTTTG | 7464 |
rs2231660 | snp | A/G/T | 0.000780795 | 0.0197433 | missense | CORO2A | GRCh38.p7 | 9:98134880 | GAACTCGTGGGCCAC[A/G/T]CGCGCAGAGTAGGCC | 7464 |
rs2231661 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CORO2A | GRCh38.p7 | 9:98133277 | TCCTGGCCAGCATGT[A/G]ACTATGAGGCCCAGG | 7464 |
rs2231662 | snp | C/T | 0.0146011 | 0.0841865 | intron-variant | CORO2A | GRCh38.p7 | 9:98132170 | GGTGAGGGCTGCACC[C/T]CACCCCTCACCATCA | 7464 |
rs2231663 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | CORO2A | GRCh38.p7 | 9:98132018 | ATGCTGACAGCCCCG[C/G]GCGAGCCCAGACCCT | 7464 |
rs2231664 | snp | A/C/T | 0.0226052 | 0.103884 | intron-variant | CORO2A | GRCh38.p7 | 9:98130926 | GGGAGGGAGGTGACC[A/C/T]CCTGGACCCCTGAGA | 7464 |
rs2231665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98130848 | GGGCAGGCCTCGCTG[A/G]CCACTCTTTCCCTGT | 7464 |
rs2231666 | snp | A/G | 0.000115391 | 0.00759487 | missense | CORO2A | GRCh38.p7 | 9:98129874 | GAGATGGCAACATCC[A/G]CTACTACGAGGTGAG | 7464 |
rs2231667 | snp | C/T | 0.021333 | 0.101051 | intron-variant | CORO2A | GRCh38.p7 | 9:98129708 | GTCAGGGCTTCAGTG[C/T]GGGGTCTGGGGAGAC | 7464 |
rs2231668 | snp | A/G/T | 0.00505293 | 0.05001 | intron-variant | CORO2A | GRCh38.p7 | 9:98128121 | TGACAGGAACATGGC[A/G/T]TGCCCAGTGGCCCCA | 7464 |
rs2231669 | snp | A/G/T | 0.0498117 | 0.149749 | intron-variant | CORO2A | GRCh38.p7 | 9:98126863 | TATGCCCATCTTCCC[A/G/T]TGGGCACCCCGTCCT | 7464 |
rs2231670 | snp | C/T | 0.0143654 | 0.0835245 | intron-variant | CORO2A | GRCh38.p7 | 9:98126835 | CCTCACATGGCTCTG[C/T]TTCCCTTCCAGACCC | 7464 |
rs2231671 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | CORO2A | GRCh38.p7 | 9:98126421 | TGGCCTGGCCTAGTC[A/G]CTTGACTCATTTTGT | 7464 |
rs2231672 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | CORO2A | GRCh38.p7 | 9:98126386 | TCATTCAACAAACAG[A/G]CAGTGAGCTCCATCT | 7464 |
rs2250494 | snp | A/C | 0.498652 | 0.0259235 | intron-variant | CORO2A | GRCh38.p7 | 9:98157036 | AGCAACACTTGCACT[A/C]AGGACAAAAGCCTGT | 7464 |
rs2275709 | snp | A/T | 0.267636 | 0.249377 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172669 | TCTGCTCACCCTTAA[A/T]CAGTTCCCCAGGCAG | 7464 |
rs2275710 | snp | C/T | 0.437259 | 0.165632 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172768 | ACCTAAATTGTTTGT[C/T]CAGGCTGGGCCTGCA | 7464 |
rs2417732 | snp | G/T | 0.31357 | 0.241783 | intron-variant | CORO2A | GRCh38.p7 | 9:98154975 | GGTTGGTATTTCTGG[G/T]TCACAGGTATATGCA | 7464 |
rs2417733 | snp | A/G | 0.364401 | 0.222289 | intron-variant | CORO2A | GRCh38.p7 | 9:98166700 | ATGAAAGCAGGGTCT[A/G]GAAGAGATATTTGCA | 7464 |
rs2476443 | snp | C/T | 0.351418 | 0.228505 | intron-variant | CORO2A | GRCh38.p7 | 9:98153999 | TAATATGATGATTTA[C/T]CTTTATAGATTTACT | 7464 |
rs2487912 | snp | A/T | 0.465368 | 0.126951 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120599 | CTAGACTTCCACTTA[A/T]AAAGCCCTCAGCTCT | 7464 |
rs2761059 | snp | C/G | 0.490618 | 0.0678448 | intron-variant | CORO2A | GRCh38.p7 | 9:98138839 | ggatcacgaggtcag[C/G]agatcgagaccatcc | 7464 |
rs2761060 | snp | C/T | 0.453087 | 0.145793 | intron-variant | CORO2A | GRCh38.p7 | 9:98147609 | atttagcaagtaaaa[C/T]acaggatgcccagta | 7464 |
rs2761061 | snp | A/C | 0.487746 | 0.0773096 | intron-variant | CORO2A | GRCh38.p7 | 9:98150564 | GGTCCCCTCTCCCAA[A/C]CCACGTCACACTCTA | 7464 |
rs2761062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171574 | CCAGCGCTGCAAGTT[A/G]CAGCAGGGAGATGGA | 7464 |
rs2795486 | snp | A/T | 0.135825 | 0.222405 | intron-variant | CORO2A | GRCh38.p7 | 9:98140886 | CCCCTACTGGAGGGG[A/T]CAACGctataaagga | 7464 |
rs2795487 | snp | C/T | 0.431177 | 0.172264 | intron-variant | CORO2A | GRCh38.p7 | 9:98141897 | CAGTAACAGAAGCTA[C/T]TATTATATGTATATG | 7464 |
rs2795488 | snp | C/T | 0.144969 | 0.226867 | intron-variant | CORO2A | GRCh38.p7 | 9:98142181 | CAGGAATGGAGCCCA[C/T]AGCTGCACTGTCTTA | 7464 |
rs2795489 | snp | A/G | 0.41507 | 0.187755 | intron-variant | CORO2A | GRCh38.p7 | 9:98147649 | ttgcagataaacaac[A/G]aatattttagcataa | 7464 |
rs2795490 | snp | G/T | 0.452965 | 0.145963 | intron-variant | CORO2A | GRCh38.p7 | 9:98147714 | atttgtAaaaataaa[G/T]tgacagtttcttata | 7464 |
rs2795491 | snp | C/T | 0.397452 | 0.201886 | intron-variant | CORO2A | GRCh38.p7 | 9:98149140 | agggtaaaggataca[C/T]agaattgcactgtac | 7464 |
rs2795492 | snp | A/G | 0.441432 | 0.160792 | intron-variant | CORO2A | GRCh38.p7 | 9:98151094 | CCCTTTGCCATTTAT[A/G]CCCTCCCTATTTATT | 7464 |
rs2795493 | snp | A/G | 0.444267 | 0.157354 | intron-variant | CORO2A | GRCh38.p7 | 9:98153534 | gcttcagcctctcgt[A/G]tagctgggactacag | 7464 |
rs2795494 | snp | A/G | 0.470521 | 0.117772 | intron-variant | CORO2A | GRCh38.p7 | 9:98153620 | TGCTATACTGCCCAG[A/G]CTATATGTCTGTAAC | 7464 |
rs2795495 | snp | A/T | 0.471388 | 0.116136 | intron-variant | CORO2A | GRCh38.p7 | 9:98154280 | gaaagttttgtagga[A/T]ttacctgtaaaacca | 7464 |
rs2985029 | snp | C/T | 0.45692 | 0.1403 | intron-variant | CORO2A | GRCh38.p7 | 9:98148134 | gcaaggtggttcatg[C/T]ctgtaatcccagctc | 7464 |
rs2985030 | snp | A/T | 0.139225 | 0.224118 | intron-variant | CORO2A | GRCh38.p7 | 9:98148212 | CCAGCCTGGCCAACA[A/T]AGCAAAACCCCATCT | 7464 |
rs3055383 | in-del | -/T/TTT/TTTT | 0.301681 | 0.2446 | intron-variant | CORO2A | GRCh38.p7 | 9:98152126 | CTGTTTTTTTTTTTT[-/T/TTT/TTTT]GTTTTTTCTTTAAGG | 7464 |
rs3059554 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177480 | ttttttttttttttt[-/TT]gagacagagtctggc | 7464 |
rs3174288 | snp | A/C/G/T | 0.000362402 | 0.0134565 | synonymous-codon, missense | CORO2A | GRCh38.p7 | 9:98126722 | GCCCCAGCCTCACCC[A/C/G/T]GGCTCTTGAATCAGA | 7464 |
rs3758261 | snp | A/G | 0.238171 | 0.24972 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174030 | AACCTCCACCTCCCA[A/G]GTTCAAGCAATTCTC | 7464 |
rs3758262 | snp | G/T | 0.238749 | 0.249747 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173958 | CGGCTAATTTTGTAT[G/T]TTTAGTAAAGACGGG | 7464 |
rs3758263 | snp | C/T | 0.145305 | 0.227022 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173946 | TATTTTTAGTAAAGA[C/T]GGGGTTTCTCCATGT | 7464 |
rs3780456 | snp | C/G | 0.23846 | 0.249734 | intron-variant | CORO2A | GRCh38.p7 | 9:98162449 | AGAGGATTGGGGGAC[C/G]GACAGAAGGGCACTG | 7464 |
rs3780457 | snp | C/T | 0.161267 | 0.233723 | intron-variant | CORO2A | GRCh38.p7 | 9:98160125 | TTAGGGCAAAGCTCC[C/T]GAAAGGAGAGTTGGA | 7464 |
rs3780458 | snp | A/C | 0.377582 | 0.214995 | intron-variant | CORO2A | GRCh38.p7 | 9:98159920 | GTGGGCTGGGTGAGC[A/C]TCTTCTTTATCTTGA | 7464 |
rs3780459 | snp | A/T | 0.451359 | 0.148171 | intron-variant | CORO2A | GRCh38.p7 | 9:98146686 | TCTCACTTCACTGAC[A/T]TGAGGCCCCTGAGGT | 7464 |
rs3780460 | snp | A/G | 0.393987 | 0.204372 | intron-variant | CORO2A | GRCh38.p7 | 9:98144788 | GTCCTCCAGCCTACC[A/G]TGCCCGCTGGCTGCT | 7464 |
rs3780461 | snp | C/G | 0.227074 | 0.248947 | intron-variant | CORO2A | GRCh38.p7 | 9:98143923 | ACTGTGCCCAGCCAA[C/G]AAGCATTTAAAAACC | 7464 |
rs3780464 | snp | C/G | 0.301932 | 0.244547 | intron-variant | CORO2A | GRCh38.p7 | 9:98143420 | CGTCCTGCCACCCCT[C/G]CCTCCCAGTCTCCAC | 7464 |
rs3780465 | snp | C/T | 0.230017 | 0.2492 | intron-variant | CORO2A | GRCh38.p7 | 9:98143376 | GATGCTCATTTGAGG[C/T]CATGACTATGATGCT | 7464 |
rs3824454 | snp | A/G | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98190862 | TGTTATTATCCCCTC[A/G]TAAAAGCAGGCAAAG | 7464 |
rs3837264 | in-del | -/CGCAGGGCAGCGCAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142852 | GGCAGCGCAGGGCAG[-/CGCAGGGCAGCGCAG]GGCAGGGCAGGGCAG | 7464 |
rs3837265 | in-del | -/T | 0.297128 | 0.245518 | intron-variant | CORO2A | GRCh38.p7 | 9:98141939 | GCTCATTCCTTTTAG[-/T]TTTTTTTTTCTCAGT | 7464 |
rs3837266 | in-del | -/TGGCTTAAGCGT/TGGCTTGAGCGT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141342 | aaaaaaaaGGGTCAG[-/TGGCTTAAGCGT/TGGCTTGAGCGT]TGGTCCCATGGAGAC | 7464 |
rs4266764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98171758 | CAGGAGCTTGCAGCG[C/T]GGGGGTGGGGAGGCT | 7464 |
rs4610873 | snp | G/T | 0.489083 | 0.0730708 | intron-variant | CORO2A | GRCh38.p7 | 9:98171751 | ATGGAGCCAGGAGCT[G/T]GCAGCGCGGGGGTGG | 7464 |
rs4742718 | snp | A/G | 0.441705 | 0.160466 | intron-variant | CORO2A | GRCh38.p7 | 9:98151964 | TGGGACCACAGGCGC[A/G]CGCCACCATGCCCGG | 7464 |
rs4743170 | snp | A/G | 0.466412 | 0.125164 | intron-variant | CORO2A | GRCh38.p7 | 9:98138500 | acccaaatgcccatc[A/G]agtgaagaatggaca | 7464 |
rs4743171 | snp | C/T | 0.452227 | 0.146984 | intron-variant | CORO2A | GRCh38.p7 | 9:98145853 | AAGTAGCTGGGACTA[C/T]AGGCATGTGCCACCA | 7464 |
rs4743172 | snp | G/T | 0.18134 | 0.240387 | intron-variant | CORO2A | GRCh38.p7 | 9:98154164 | tgtcctccttgtctg[G/T]ttttggtatcaaggt | 7464 |
rs4743173 | snp | G/T | 0.470618 | 0.117591 | intron-variant | CORO2A | GRCh38.p7 | 9:98155320 | TTTTGCTATTTTCTT[G/T]AAGGGAAATTTTTAT | 7464 |
rs4743174 | snp | C/T | 0.493613 | 0.0561475 | intron-variant | CORO2A | GRCh38.p7 | 9:98167971 | GTCTTTAAATTTCCA[C/T]TGTAAAAGATTTAAG | 7464 |
rs4743175 | snp | C/G | 0.492966 | 0.0588865 | intron-variant | CORO2A | GRCh38.p7 | 9:98168291 | ATGGACAGCACCACC[C/G]TATCATTTCCTATCT | 7464 |
rs4743176 | snp | A/C | 0.492918 | 0.0590819 | intron-variant | CORO2A | GRCh38.p7 | 9:98168377 | CTACAAATACACATA[A/C]TAGCTAACGCCTATA | 7464 |
rs4743177 | snp | A/G | 0.493013 | 0.058691 | intron-variant | CORO2A | GRCh38.p7 | 9:98168395 | GCTAACGCCTATATT[A/G]CTGACTAGGTGTTAA | 7464 |
rs4743178 | snp | C/G | 0.493013 | 0.058691 | intron-variant | CORO2A | GRCh38.p7 | 9:98168398 | AACGCCTATATTACT[C/G]ACTAGGTGTTAAGTA | 7464 |
rs4743179 | snp | C/T | 0.260227 | 0.249791 | intron-variant | CORO2A | GRCh38.p7 | 9:98171545 | AGCTCAATTCAGGGT[C/T]ATCAGGGCTAAAGCC | 7464 |
rs4743182 | snp | A/G | 0.493613 | 0.0561475 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187520 | tatttctcacagttc[A/G]ggaggatggaagtcc | 7464 |
rs4743183 | snp | C/G | 0.295088 | 0.245901 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187605 | aatggcgccttctta[C/G]tgtgtcctcatgtgg | 7464 |
rs4743184 | snp | A/G | 0.27008 | 0.249192 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193432 | ACAGAGATATTAAGT[A/G]CCTAGGTTAAGATCA | 7464 |
rs6478581 | snp | A/T | 0.49614 | 0.0437598 | intron-variant | CORO2A | GRCh38.p7 | 9:98161939 | AGCCACTCTCCATCC[A/T]GGAGGAGTGAGGAGG | 7464 |
rs6478582 | snp | A/G | 0.284471 | 0.247612 | intron-variant | CORO2A | GRCh38.p7 | 9:98162997 | CACATCAAAGCCACA[A/G]CAGGCATTCTCAGGT | 7464 |
rs6478592 | snp | A/G | 0.456332 | 0.141164 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185803 | GCAGGTGGGCCAGGA[A/G]AGACCCTGGCCCAAG | 7464 |
rs6478593 | snp | C/T | 0.496937 | 0.0390173 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186281 | GAGAGGGGTGGCTGG[C/T]GGGGGGAGGGGCTAG | 7464 |
rs6478595 | snp | A/T | 0.484771 | 0.0859212 | intron-variant | CORO2A | GRCh38.p7 | 9:98189891 | GCAACTCCtttattt[A/T]tttttttttttgaga | 7464 |
rs6478596 | snp | C/G | 0.481087 | 0.0953875 | intron-variant | CORO2A | GRCh38.p7 | 9:98190069 | tttatatttttagta[C/G]agacaggatttcatc | 7464 |
rs6478597 | snp | A/G | 0.481242 | 0.0950111 | intron-variant | CORO2A | GRCh38.p7 | 9:98190105 | gcccaggctggtctc[A/G]aactctagacctcag | 7464 |
rs6478598 | snp | C/T | 0.461148 | 0.133852 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192726 | CCCAAGGTCCGCCCT[C/T]TTGCCCGCCCCGCGG | 7464 |
rs6478599 | snp | C/T | 0.461148 | 0.133852 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192728 | CAAGGTCCGCCCTTT[C/T]GCCCGCCCCGCGGGT | 7464 |
rs7022366 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | CORO2A | GRCh38.p7 | 9:98155016 | ctttccaaaacaggt[A/G]tgccagtttacactc | 7464 |
rs7023194 | snp | A/G | 0.272241 | 0.249009 | intron-variant | CORO2A | GRCh38.p7 | 9:98172527 | CCCACTTCTGAGATC[A/G]ACCCCATGCCTCACT | 7464 |
rs7023750 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142866 | cctgcgctgccctgc[C/G]ctgccctgcgctgcc | 7464 |
rs7029397 | snp | A/G | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98191773 | TGTCACCCCTCTGAG[A/G]TCCAGGCGTGGCCGC | 7464 |
rs7029784 | snp | C/T | 0.32885 | 0.23724 | intron-variant | CORO2A | GRCh38.p7 | 9:98191370 | CCAGGGCAGACACCT[C/T]GGCTCCCTCTTCTTG | 7464 |
rs7030682 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | CORO2A | GRCh38.p7 | 9:98161956 | GAGGAGTGAGGAGGC[C/T]GTGAGAGGCCTGGGC | 7464 |
rs7031271 | snp | A/G | 0.451359 | 0.148171 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187232 | agcttgcagtgagcc[A/G]agatcgtgctgctgc | 7464 |
rs7032548 | snp | C/T | 0.466515 | 0.124985 | intron-variant | CORO2A | GRCh38.p7 | 9:98165217 | TCACACCTCAGCCTC[C/T]CAAAGTGCTGGGATG | 7464 |
rs7032570 | snp | C/T | 0.39979 | 0.200158 | intron-variant | CORO2A | GRCh38.p7 | 9:98165265 | TGCCTGGCTTACACG[C/T]AACAATTCTATTGTA | 7464 |
rs7033797 | snp | C/G | 0.191775 | 0.243125 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192785 | CACGACCCCGACCGC[C/G]CTCCTGGCTCCCCGG | 7464 |
rs7034547 | snp | A/G | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98191089 | AAAATCCCTGGGTGC[A/G]GGGCAGGTCATGAAG | 7464 |
rs7034562 | snp | C/G | 0.439363 | 0.163222 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187362 | tactcaggaggctga[C/G]atgggagaatcactt | 7464 |
rs7034681 | snp | A/T | 0.32153 | 0.239548 | intron-variant | CORO2A | GRCh38.p7 | 9:98177765 | AAAAAAAACAAACTG[A/T]GCTCACACCCCATTA | 7464 |
rs7034835 | snp | A/C/T | 0.0520825 | 0.152737 | intron-variant | CORO2A | GRCh38.p7 | 9:98162724 | GTGGGTGTGCATGCA[A/C/T]GTGTGCATCCCTTTG | 7464 |
rs7035365 | snp | A/T | 0.23031 | 0.249223 | intron-variant | CORO2A | GRCh38.p7 | 9:98178478 | CTTAGAGTGGTGAAT[A/T]TAATTTGTAAATCCA | 7464 |
rs7038290 | snp | A/G | 0.41507 | 0.187755 | intron-variant | CORO2A | GRCh38.p7 | 9:98154331 | tatgtgTTTGTGTGt[A/G]tatatatatatatat | 7464 |
rs7038728 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | CORO2A | GRCh38.p7 | 9:98134097 | TCCCGAGGTGTCTCT[A/G]TAAACCCCtatagtg | 7464 |
rs7038945 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98188442 | ttgtttaatatcagc[A/G]ccttccccctttccc | 7464 |
rs7039895 | snp | A/G | 0.0391387 | 0.134304 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121775 | ACCTGTGTTAGAACA[A/G]CATGTGTCACTGAGT | 7464 |
rs7040921 | snp | A/G | 0.215446 | 0.2476 | intron-variant | CORO2A | GRCh38.p7 | 9:98176736 | CTCCTCAGCAGAGCA[A/G]GTCCCCAAAAGGATC | 7464 |
rs7045584 | snp | A/G | 0.230896 | 0.249269 | intron-variant | CORO2A | GRCh38.p7 | 9:98178086 | GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 7464 |
rs7047096 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98156475 | gatatatttcatttt[A/G]tcaattccaaggatt | 7464 |
rs7468249 | snp | C/G | | | utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98192577 | GATGACTGCCGCGCA[C/G]GTGGCGGTGGCGGCG | 7464 |
rs7847003 | snp | A/G | 0.239037 | 0.24976 | intron-variant | CORO2A | GRCh38.p7 | 9:98171450 | ATGCTGGGCACTGTA[A/G]GGGAGATGCATGGGC | 7464 |
rs7847475 | snp | A/G | 0.316243 | 0.241064 | intron-variant | CORO2A | GRCh38.p7 | 9:98148983 | taattgtcatctggg[A/G]ttaaggagggaatgg | 7464 |
rs7848016 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | CORO2A | GRCh38.p7 | 9:98148646 | ctattcaggaggctg[A/C]cgtaagaggattgct | 7464 |
rs7851013 | snp | C/G | 0.115788 | 0.21092 | intron-variant | CORO2A | GRCh38.p7 | 9:98154729 | ttggcttatttcact[C/G]aactttatctttctg | 7464 |
rs7854562 | snp | A/G | 0.489083 | 0.0730708 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186003 | AGGGCTGGCTAGAGG[A/G]ACAAGACTCTTGGGC | 7464 |
rs7860937 | snp | A/G | 0.364401 | 0.222289 | intron-variant | CORO2A | GRCh38.p7 | 9:98166169 | AATCAGGAAAAAAAC[A/G]CAGGACATCCTACAT | 7464 |
rs7861431 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | CORO2A | GRCh38.p7 | 9:98132765 | CCAGAGCTGAGGCAC[A/G]CCAACAAGCTTTgga | 7464 |
rs7862309 | snp | C/T | 0.444799 | 0.156695 | intron-variant | CORO2A | GRCh38.p7 | 9:98162854 | CATTTTCCCTACAAG[C/T]AGGCACTTGCCCACA | 7464 |
rs7865264 | snp | A/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123828 | gcctggttaattttt[A/T]atttttagtggagac | 7464 |
rs7865848 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148411 | aaaaaaaaaaaaaaa[A/T]aagataaataaaTAA | 7464 |
rs7866005 | snp | C/G | 0.291493 | 0.246533 | intron-variant | CORO2A | GRCh38.p7 | 9:98133438 | GTGGTGAAAGGAAAA[C/G]GCCACCTGCCTCTGA | 7464 |
rs7866160 | snp | A/G | 0.149665 | 0.228982 | intron-variant | CORO2A | GRCh38.p7 | 9:98154877 | gttttgcaataatac[A/G]aacaatgctactatg | 7464 |
rs7868004 | snp | C/T | 0.246769 | 0.249979 | intron-variant | CORO2A | GRCh38.p7 | 9:98167047 | agttagaggctgcag[C/T]aagctatgattatac | 7464 |
rs7869422 | snp | G/T | 0.152334 | 0.230133 | intron-variant | CORO2A | GRCh38.p7 | 9:98154962 | ggtataaacctatgg[G/T]tggtatttctgggtc | 7464 |
rs7870439 | snp | G/T | 0.327914 | 0.237549 | intron-variant | CORO2A | GRCh38.p7 | 9:98189556 | TTGCTACTGAGATTT[G/T]TTCACTCTAAGAGGT | 7464 |
rs9299274 | snp | A/T | 0.456803 | 0.140473 | intron-variant | CORO2A | GRCh38.p7 | 9:98147826 | TCACCCAAAAATATG[A/T]ACACAAATGTTTGTA | 7464 |
rs9776207 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163339 | ggataacaggcgcat[C/G]ccactgtgccccact | 7464 |
rs9918998 | snp | A/T | 0.335788 | 0.23482 | intron-variant | CORO2A | GRCh38.p7 | 9:98181463 | TTATAGGCGTGAGCC[A/T]CGGTGCCTGGCTCCA | 7464 |
rs10118043 | snp | A/G | 0.388964 | 0.20782 | intron-variant | CORO2A | GRCh38.p7 | 9:98161190 | GGTGTGGCCACAGAG[A/G]AGGAGGCAGGACCCA | 7464 |
rs10124412 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | CORO2A | GRCh38.p7 | 9:98161426 | GGGTGTGGTGGCGCG[C/T]GCCTGTAGTCCCAGC | 7464 |
rs10217347 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | CORO2A | GRCh38.p7 | 9:98183302 | CCCCAAGTCTTTGTC[C/T]CAAGAAAAGAGTCCT | 7464 |
rs10217398 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | CORO2A | GRCh38.p7 | 9:98184938 | TTGTAGTTCATAAAG[C/T]GCCTCCTTACTTTTA | 7464 |
rs10217520 | snp | A/G | 0.409721 | 0.192325 | intron-variant | CORO2A | GRCh38.p7 | 9:98183876 | tgaggcacaagaatc[A/G]cttgaacccgggagg | 7464 |
rs10491723 | snp | A/G | 0.494358 | 0.0528145 | intron-variant | CORO2A | GRCh38.p7 | 9:98165350 | ATCCATTTCTTAAAG[A/G]GCCCAACATACCGAA | 7464 |
rs10491724 | snp | A/G | 0.17138 | 0.237316 | intron-variant | CORO2A | GRCh38.p7 | 9:98165569 | ACCTCTCAGGGAAAT[A/G]ACCAAGAGCAGAAAG | 7464 |
rs10532253 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187476 | AAAAAAAAAAAAAAA[-/A]TGTAGGTGCTTTATC | 7464 |
rs10634002 | snp | A/G | 0.277778 | 0.248452 | intron-variant | CORO2A | GRCh38.p7 | 9:98163768 | AGAGAGAGAGAGAGA[A/G]AGAGAGAAAGAGACA | 7464 |
rs10666189 | in-del | -/AC | 0.497502 | 0.035255 | intron-variant | CORO2A | GRCh38.p7 | 9:98149950 | TTTTTTTTTTTTGAG[-/AC]AGAGTCTCGCACTGT | 7464 |
rs10689817 | in-del | -/CGGGGGGG | 0.0142736 | 0.0832652 | intron-variant | CORO2A | GRCh38.p7 | 9:98192481 | TCCGGGAGCTGCAGC[-/CGGGGGGG]CGCAGCGCGCACGTC | 7464 |
rs10760183 | snp | A/G | 0.400682 | 0.199487 | intron-variant | CORO2A | GRCh38.p7 | 9:98184317 | AGTGCTGGGATTACC[A/G]GGAGGAGCCACCATG | 7464 |
rs10818514 | snp | A/T | 0.110167 | 0.207236 | intron-variant | CORO2A | GRCh38.p7 | 9:98135542 | TGAGGGCCTGAGAAG[A/T]GGTGCTGGGACTTCC | 7464 |
rs10818534 | snp | A/G | 0.498158 | 0.0302955 | intron-variant | CORO2A | GRCh38.p7 | 9:98160460 | ATCAGAAAGGGATTT[A/G]TTTGGTGTCTATAAG | 7464 |
rs10818540 | snp | C/T | 0.238171 | 0.24972 | intron-variant | CORO2A | GRCh38.p7 | 9:98164494 | ATAAGGCCACCCTGC[C/T]GCCAACCTAGGCCTC | 7464 |
rs10818541 | snp | C/T | 0.471673 | 0.115589 | intron-variant | CORO2A | GRCh38.p7 | 9:98164879 | GGGAGGCAGGACTTA[C/T]AGCGCTAAACTGGGG | 7464 |
rs10818543 | snp | C/T | 0.475259 | 0.108435 | intron-variant | CORO2A | GRCh38.p7 | 9:98165066 | CTCAACCTCCTGGGC[C/T]TGCGCAATCCTCTGG | 7464 |
rs10818575 | snp | C/T | 0.449091 | 0.151204 | intron-variant | CORO2A | GRCh38.p7 | 9:98182864 | CTGGGATGCAACTTA[C/T]AGTTTCTGTTGCTTT | 7464 |
rs10818581 | snp | C/T | 0.205723 | 0.246048 | intron-variant | CORO2A | GRCh38.p7 | 9:98183534 | TATCATTATAACTTG[C/T]ATTGCATACATAGTT | 7464 |
rs10818584 | snp | A/T | 0.313814 | 0.241719 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186269 | AAATGATGCCAGGAG[A/T]GGGGTGGCTGGCGGG | 7464 |
rs10818585 | snp | C/T | 0.494651 | 0.0514399 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186952 | CTCTGCACCTGTCTT[C/T]GTCCGTTGCTGCAGC | 7464 |
rs10818586 | snp | A/G | 0.488846 | 0.0738428 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187079 | GGTCAGGAGATTGAG[A/G]CCATCCTGGCTAACA | 7464 |
rs10985135 | snp | C/G | 0 | 0 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122371 | gctcccaagggaatt[C/G]taatgtacacagctt | 7464 |
rs10985139 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123501 | TCTCTCTCTCTTTTT[G/T]TTTTTTTTTTTGGAG | 7464 |
rs10985151 | snp | A/G | 0.229136 | 0.249128 | intron-variant | CORO2A | GRCh38.p7 | 9:98127485 | GAGGGACCTGGGTGG[A/G]GGTTGCTGCCTGGAG | 7464 |
rs10985166 | snp | C/T | 0.111928 | 0.208413 | intron-variant | CORO2A | GRCh38.p7 | 9:98133766 | CTCCCCACAACAATT[C/T]TAGTTATTTATTTTT | 7464 |
rs10985203 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149410 | CTCCTGGGTGTGTTA[A/G]TCCATTTTGCATTGC | 7464 |
rs10985208 | snp | C/T | 0.314787 | 0.241459 | intron-variant | CORO2A | GRCh38.p7 | 9:98150607 | AATTTATTTTCTTTA[C/T]ATCAGTTGTTAGTAC | 7464 |
rs10985211 | snp | C/T | 0.314057 | 0.241654 | intron-variant | CORO2A | GRCh38.p7 | 9:98151808 | ATGCACCACCATGCC[C/T]GGCTAATTTTTTTTT | 7464 |
rs10985238 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159899 | GTTTGGCTGGGCCTA[C/T]GCTGGTCAAGATAAA | 7464 |
rs10985248 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163724 | GGGgtgtgtgtgtgt[A/G]tgtgtatgtgtgtgt | 7464 |
rs10985257 | snp | A/C | 0.302184 | 0.244493 | intron-variant | CORO2A | GRCh38.p7 | 9:98164973 | GGTCTAGGTGTAACA[A/C]TTCTTTTTTTTTTGA | 7464 |
rs10985266 | snp | C/T | 0.238749 | 0.249747 | intron-variant | CORO2A | GRCh38.p7 | 9:98165961 | TGGATGGGTTGGCAA[C/T]ACCTGAACCCACTGC | 7464 |
rs10985270 | snp | C/G | 0.233818 | 0.249476 | intron-variant | CORO2A | GRCh38.p7 | 9:98166533 | gcaagcaaacaattt[C/G]atttgaaacaatCTG | 7464 |
rs10985279 | snp | A/G | 0.23846 | 0.249734 | intron-variant | CORO2A | GRCh38.p7 | 9:98168665 | TAGTGTTCAAAAGAC[A/G]TTGGCTAGTAAGATT | 7464 |
rs10985302 | snp | G/T | 0.356597 | 0.226135 | intron-variant | CORO2A | GRCh38.p7 | 9:98171878 | GGGAGGCATCAAAGT[G/T]TGTAACTGGGGGTGT | 7464 |
rs10985325 | snp | C/T | 0.283158 | 0.247791 | intron-variant | CORO2A | GRCh38.p7 | 9:98176180 | CAAAACCCTCTGAAC[C/T]GAATGAAAGCAGAGA | 7464 |
rs10985337 | snp | A/G | 0.194278 | 0.243711 | intron-variant | CORO2A | GRCh38.p7 | 9:98180919 | AGCTCCAGGGATGGT[A/G]TGGGGGCCATGTGAT | 7464 |
rs10985340 | snp | A/G | 0.370974 | 0.218781 | intron-variant | CORO2A | GRCh38.p7 | 9:98182438 | AGCTCCTTCCTGTTC[A/G]TTATCTCCCCAGCCC | 7464 |
rs10985355 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188785 | AGAAAACAACAACAA[A/C]AACAAAAAACAACAA | 7464 |
rs10985358 | snp | C/T | 0.322959 | 0.239117 | intron-variant | CORO2A | GRCh38.p7 | 9:98189268 | TCACCTACTCCTGGC[C/T]CTTTAGACCAGGTGT | 7464 |
rs10985359 | snp | C/T | 0.248188 | 0.249993 | intron-variant | CORO2A | GRCh38.p7 | 9:98189586 | TTGGCTGTCAGAGCT[C/T]AAACAAATTCAGCAA | 7464 |
rs10985360 | snp | A/G | 0.274661 | 0.248781 | intron-variant | CORO2A | GRCh38.p7 | 9:98189658 | TCCAGAGAGGGGAAC[A/G]GATCGGCCCAAGGTC | 7464 |
rs10985361 | snp | A/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98189895 | CTCCTTTATTTTTTT[A/T]TTTTTTTGAGATGGA | 7464 |
rs10985365 | snp | A/G | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98191162 | CTGCTCCCTCAAACA[A/G]GGCAGGCATCAGGGA | 7464 |
rs10985366 | snp | C/G | 0.474363 | 0.110278 | intron-variant | CORO2A | GRCh38.p7 | 9:98191795 | CGTGGCCGCCAGTCA[C/G]CCCTTGTCACACCAG | 7464 |
rs10985367 | snp | A/G | 0.269809 | 0.249214 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192853 | CGCGCACACGCCGCA[A/G]TGATTGGGGCGGGCT | 7464 |
rs10985369 | snp | C/T | 0.266546 | 0.249452 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194013 | ATATGGATGGCTGGG[C/T]GCAGTGGCTCATGCT | 7464 |
rs10985370 | snp | A/G | 0.266546 | 0.249452 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194237 | AGGTGGCAGTGAGCC[A/G]AGATCACATCACTGC | 7464 |
rs11281388 | in-del | -/GGGGGGCG | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98192483 | CGGGAGCTGCAGCCG[-/GGGGGGCG]CAGCGCGCACGTCCC | 7464 |
rs11304742 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144207 | GAAAAAAAAAAAAAA[-/A]GCTTTTCTTTAGAAA | 7464 |
rs11345726 | in-del | -/C | 0.0861826 | 0.188849 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192695 | GGCGGGGCCGGAGGG[-/C]GGGGCGGGGGCCTGG | 7464 |
rs11379239 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155364 | TTTTTATTGCTCAAT[-/T]TTTTTTTTTTTTTTT | 7464 |
rs11379261 | in-del | -/TG/TTG/TTTG | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98152135 | TTGCTGTTTTTTTTT[-/TG/TTG/TTTG]TTTGTTTTTTCTTTA | 7464 |
rs11427674 | in-del | -/T | 0.411074 | 0.191194 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173547 | TTGCTTTCTTAAGTC[-/T]TCTTCTCAACATATA | 7464 |
rs11449086 | in-del | -/A | 0.328616 | 0.237317 | intron-variant | CORO2A | GRCh38.p7 | 9:98189705 | GACTTCAATCTGGAA[-/A]TCTATGTCTGCTGAC | 7464 |
rs11787586 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133351 | GCCTGGCCAAGAAGC[C/T]TCAGTGGGAGGATGA | 7464 |
rs11788080 | snp | C/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98127452 | CGGGAGAGTGGCTCA[C/G]GACAGGCAGAGTGGG | 7464 |
rs11789051 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98171211 | GGACAGAGAGGGACA[C/T]TGAGGCTCAGAGAGG | 7464 |
rs11790033 | snp | C/T | 0.496874 | 0.0394129 | intron-variant | CORO2A | GRCh38.p7 | 9:98148469 | ACACATAATTGAggc[C/T]aggtgcagtggctca | 7464 |
rs11791308 | snp | C/T | 0.271432 | 0.24908 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186996 | CATAAATTGGGTGCT[C/T]TGGCCAGGCGCGGTG | 7464 |
rs11791479 | snp | C/T | 0.449599 | 0.150533 | intron-variant | CORO2A | GRCh38.p7 | 9:98182125 | ATTACTGTCCATCTC[C/T]CGTTTGGTCTGTGAG | 7464 |
rs11791841 | snp | G/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98169850 | TTAGCAGGGCTCTTA[G/T]AATGCCCCTTCCTGT | 7464 |
rs11792904 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | CORO2A | GRCh38.p7 | 9:98171382 | GCCTCAGGGACCTGG[C/G]GCCCAGAGTCAGTTC | 7464 |
rs11794697 | snp | A/G | 0.101658 | 0.201233 | intron-variant | CORO2A | GRCh38.p7 | 9:98144970 | GGACCGCCCAGAGGA[A/G]GCTGGGATTGAGCAG | 7464 |
rs11794723 | snp | A/G | 0.178282 | 0.239492 | intron-variant | CORO2A | GRCh38.p7 | 9:98128309 | TAGGGTAGGCTGCTC[A/G]GATGGGAAAGGCCCT | 7464 |
rs11795235 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159234 | tggctaattaaaaaa[A/T]ttttttttcttgcca | 7464 |
rs11999011 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159490 | ATCTAAACGGCACCT[C/T]CCAGCTTCCCCAGCA | 7464 |
rs12000974 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CORO2A | GRCh38.p7 | 9:98160768 | TGATGCTCACCAGAC[G/T]TCCCATTGCTCCCCT | 7464 |
rs12005005 | snp | A/C/G | 0.0126979 | 0.078662 | intron-variant | CORO2A | GRCh38.p7 | 9:98160689 | CGCTCCAGGCCCCCC[A/C/G]ACTCCTCCCTCACCT | 7464 |
rs12005285 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173985 | gccgggcgtggtggc[A/G]catgcctgtaatccc | 7464 |
rs12238262 | snp | G/T | 0.322959 | 0.239117 | intron-variant | CORO2A | GRCh38.p7 | 9:98189328 | AGGAGGCAAGGCATG[G/T]ATTATAGACTTAAAA | 7464 |
rs12238311 | snp | A/G | 0.242488 | 0.249887 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122614 | AAAAGCTTTCAGGCT[A/G]AAAGGGAACTTTGGG | 7464 |
rs12338195 | snp | C/T | 0.33303 | 0.235809 | intron-variant | CORO2A | GRCh38.p7 | 9:98166582 | aggaatgcaaaaggg[C/T]ttagttgctatgaaa | 7464 |
rs12340297 | snp | C/T | 0.301177 | 0.244706 | intron-variant | CORO2A | GRCh38.p7 | 9:98142391 | TGCTCTGAGGGAGCA[C/T]CAGTGAGTGCTCTGT | 7464 |
rs12341046 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125902 | tttgtatttttagta[A/G]agacggggtttcgcc | 7464 |
rs12344078 | snp | A/C | 0.021333 | 0.101051 | intron-variant | CORO2A | GRCh38.p7 | 9:98151081 | TGCTTGTGCCCTTCC[A/C]TTTGCCATTTATACC | 7464 |
rs12344700 | snp | C/T | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98191240 | CGGCTCTCCTCACTC[C/T]GGACCTCTCAGACGG | 7464 |
rs12345418 | snp | C/T | 0.089084 | 0.191327 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187835 | ATTCAAATCTGGCCA[C/T]GTTCCTACCCAATTC | 7464 |
rs12346761 | snp | A/C | 0.0898077 | 0.191933 | intron-variant | CORO2A | GRCh38.p7 | 9:98189246 | CAGTTTGACCACAGA[A/C]GCAAAGTCACCTACT | 7464 |
rs12348326 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | CORO2A | GRCh38.p7 | 9:98184762 | ACTTAAATCAAGGGG[C/T]GTGTGGTTAATGGCG | 7464 |
rs12349273 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98190816 | ACTTAAGCCTGTGCG[G/T]CGGAGCTGGGCTCAT | 7464 |
rs12375846 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127854 | aaaaaaaGAATTGCA[A/G]AGGTAGGGGTGGGGA | 7464 |
rs12375882 | snp | A/G | 0 | 0 | stop-gained | CORO2A | GRCh38.p7 | 9:98128173 | TGCCTTCCTCACCTC[A/G]ATTCATCCCGCTGAG | 7464 |
rs12378662 | snp | A/C | 0.101658 | 0.201233 | intron-variant | CORO2A | GRCh38.p7 | 9:98148811 | cacacacaaaacaca[A/C]aaaaaaaTGATCAAT | 7464 |
rs12379176 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182091 | CTCTCTCCTCCTCCA[A/G]ATTCTGTGGGACTCT | 7464 |
rs12550850 | snp | C/G | 0.492966 | 0.0588865 | intron-variant | CORO2A | GRCh38.p7 | 9:98169138 | CAGCGAGGCAGAAGC[C/G]GTCTGCAGCCGGCAA | 7464 |
rs12551204 | snp | C/G | 0.251014 | 0.249998 | intron-variant | CORO2A | GRCh38.p7 | 9:98170036 | GACCCCTATTTGTCT[C/G]TGTGCCGTAGCATTA | 7464 |
rs12551475 | snp | A/G | 0.360842 | 0.224085 | intron-variant | CORO2A | GRCh38.p7 | 9:98161469 | TGAGGCAGGAGAATC[A/G]CTTGAACCGGGAATG | 7464 |
rs12552199 | snp | A/T | 0.450734 | 0.149016 | intron-variant | CORO2A | GRCh38.p7 | 9:98163743 | GTATGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 7464 |
rs12552786 | snp | A/C | 0.154993 | 0.231244 | intron-variant | CORO2A | GRCh38.p7 | 9:98181115 | AAAATGGTGGACAAT[A/C]ACCAGCCCTGGGAAG | 7464 |
rs12555858 | snp | A/G | 0.266819 | 0.249434 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194526 | CACCACACAAGCTCA[A/G]GCAATCCTCCCACCT | 7464 |
rs12684568 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120638 | ATCCTTGGTCTCCGC[A/C]CTGCCTATGCTCCAC | 7464 |
rs12684691 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163772 | agagagagagagaga[A/G]agaaagagacagaga | 7464 |
rs12685910 | snp | A/T | 0.444444 | 0.157135 | intron-variant | CORO2A | GRCh38.p7 | 9:98150997 | TTCACAGATTATTTG[A/T]TCTGGCCAGACAGCT | 7464 |
rs12686425 | snp | A/C | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98177852 | GAGTGAGATTCATCA[A/C]TAACCAGAGTGACTG | 7464 |
rs13283098 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172293 | tgagctcgaccccac[A/G]ccccacttccgagct | 7464 |
rs13284155 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98172253 | cccacgccctacttc[C/T]gagctcagtcccaca | 7464 |
rs13284304 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172328 | cccacaccccacttc[C/T]aagctcagccccaca | 7464 |
rs13284350 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126210 | ccggctaatttttgt[A/T]tttttagtagagatg | 7464 |
rs13284858 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172329 | ccacaccccacttcc[A/G]agctcagccccacac | 7464 |
rs13287241 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98154352 | atatatatatatata[C/T]acacaaatacatata | 7464 |
rs13288104 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126056 | tttttttttttttaa[A/G]atggagtcttgctct | 7464 |
rs13288117 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126080 | ttgctctgttgccca[A/G]gctggagtgcagtgg | 7464 |
rs13288246 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126092 | ccaggctggagtgca[A/G]tggtgtgatcttggc | 7464 |
rs13288286 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126185 | ggactacaggtgtac[C/G]ccaccacacccggct | 7464 |
rs13288505 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126209 | cccggctaatttttg[A/T]atttttagtagagat | 7464 |
rs13289432 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126126 | ctgcaacctccacct[C/T]ccaatttcaagccat | 7464 |
rs13289447 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126158 | ctcctgcctcaacct[C/T]tcaagtagctgggac | 7464 |
rs13290017 | snp | A/C | | | utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98192667 | CGCCGCCGCCTCCCC[A/C]TGCAgcccggcgggc | 7464 |
rs13290961 | snp | G/T | 0.462144 | 0.132269 | intron-variant | CORO2A | GRCh38.p7 | 9:98161478 | AGAATCACTTGAACC[G/T]GGAATGCGGAGGTTG | 7464 |
rs13290964 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127819 | cgagactctgtctca[A/G]aaaaaaaaaaaaaaa | 7464 |
rs13300050 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | CORO2A | GRCh38.p7 | 9:98165604 | GAGATGGTGTGACCT[C/T]GAGGGACTGCTAACA | 7464 |
rs13302862 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172285 | cccacttctgagctc[A/G]accccacgccccact | 7464 |
rs13440247 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | CORO2A | GRCh38.p7 | 9:98147061 | cccttgagcccaaga[A/G]tttgagaccagcctg | 7464 |
rs16913017 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CORO2A | GRCh38.p7 | 9:98133720 | GAAAGCGCTGTGGAT[C/T]GGAAGAGCGAGGGCC | 7464 |
rs16913404 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | CORO2A | GRCh38.p7 | 9:98163871 | AGCTGCAGGGTGGCT[A/G]AAACTGAACCCAAAC | 7464 |
rs16913411 | snp | C/T | 0.187053 | 0.241946 | intron-variant | CORO2A | GRCh38.p7 | 9:98164251 | CGCTCTATGTGAAGG[C/T]GCTCTACAAAGGCTG | 7464 |
rs16913432 | snp | A/G | 0.1652 | 0.235179 | intron-variant | CORO2A | GRCh38.p7 | 9:98165480 | TGGTGCTTATTCTGC[A/G]CCAAGCCGTGTCAGG | 7464 |
rs16913514 | snp | C/T | 0.127599 | 0.217986 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174439 | CTCTTCATTGACACA[C/T]GTAAACAAAAACATT | 7464 |
rs16913573 | snp | C/T | 0.320575 | 0.239832 | intron-variant | CORO2A | GRCh38.p7 | 9:98179033 | AGTCTAGCTCTTTAC[C/T]GGTCCTTTTACTTTA | 7464 |
rs16913575 | snp | A/G | 0.419135 | 0.184101 | intron-variant | CORO2A | GRCh38.p7 | 9:98179624 | GATGTGAGGCAAGCA[A/G]GGAAGGGGAAGTGGC | 7464 |
rs16913581 | snp | C/T | 0.111224 | 0.207945 | intron-variant | CORO2A | GRCh38.p7 | 9:98180217 | CCAAACCAGACCCTA[C/T]GTTCATCGCATCCCA | 7464 |
rs16913593 | snp | A/T | 0.258288 | 0.249863 | intron-variant | CORO2A | GRCh38.p7 | 9:98181625 | ATCTGAGCTGCACAC[A/T]TCACGGTGCTTTCAG | 7464 |
rs16913609 | snp | A/G | 0.121717 | 0.214577 | intron-variant | CORO2A | GRCh38.p7 | 9:98182216 | AGAAAGTAATCAATC[A/G]TGAACAAAGGTCCTA | 7464 |
rs16913615 | snp | A/G | 0.438806 | 0.163867 | intron-variant | CORO2A | GRCh38.p7 | 9:98184441 | CTATGTCTGCATGCT[A/G]GGGAAAGATTCTTTT | 7464 |
rs16913616 | snp | C/T | 0.354665 | 0.227036 | intron-variant | CORO2A | GRCh38.p7 | 9:98184461 | AAGATTCTTTTCTCA[C/T]ATCCAAACCCAAACA | 7464 |
rs16913619 | snp | C/G | 0.354881 | 0.226936 | intron-variant | CORO2A | GRCh38.p7 | 9:98184527 | TGACATGGTGGCCCT[C/G]TCTCTAAACAGACTG | 7464 |
rs16913640 | snp | A/G | 0.45574 | 0.142025 | intron-variant | CORO2A | GRCh38.p7 | 9:98185294 | GGGTCTAGCTTGTCT[A/G]CATTCACACTCCCCA | 7464 |
rs16913644 | snp | C/T | 0.208779 | 0.246578 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185514 | GCATCCCTTGTTGTC[C/T]GCAATCTTAGACTCC | 7464 |
rs17201968 | snp | A/C | 0.116138 | 0.211142 | intron-variant | CORO2A | GRCh38.p7 | 9:98133435 | CTAGTGGTGAAAGGA[A/C]AACGCCACCTGCCTC | 7464 |
rs17202687 | snp | C/T | 0.178785 | 0.239642 | intron-variant | CORO2A | GRCh38.p7 | 9:98164193 | CAAGTTACCCAGTTA[C/T]TTCAAAAACCGAAAA | 7464 |
rs17807775 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121721 | CTTCTCTGAGGCTAG[A/G]TCTTTGATTCTGAAC | 7464 |
rs28635946 | snp | A/G | 0.191147 | 0.242974 | intron-variant | CORO2A | GRCh38.p7 | 9:98192300 | GCCGTCGGGAGCCCG[A/G]ACCTCGAGGCGGCCC | 7464 |
rs28667685 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CORO2A | GRCh38.p7 | 9:98135183 | TGAGCAGGGGCCAGC[A/G]CTGACCAGGGATGAG | 7464 |
rs28703824 | snp | A/G | 0.304438 | 0.244001 | intron-variant | CORO2A | GRCh38.p7 | 9:98192147 | CAGCCAAGAGGGGGA[A/G]GGTCCCGACAAGAGT | 7464 |
rs28775392 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148097 | ATTAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAGA | 7464 |
rs28797623 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148096 | TATTAAAAAAAAAAA[A/G]GAAAAAAAAAAAAAG | 7464 |
rs34014018 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128113 | CAATTGCTTGGGGCC[-/A]CTGGGCACGCCATGT | 7464 |
rs34019657 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135968 | GAAGCAGAGAAGACT[-/C]CCCCACTGCTAGAGG | 7464 |
rs34087370 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148394 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs34090994 | in-del | -/AC/ACAC/ACACAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158836 | ATTAAAAAGAAGAAA[-/AC/ACAC/ACACAC]ACACACACACACACA | 7464 |
rs34107526 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170957 | CTGTCCTGAGAAGGT[-/G]CTTGTCCTGCCTGGA | 7464 |
rs34128165 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140380 | AACAGGGTGGACTCA[-/G]GGGAACACCCAACCT | 7464 |
rs34162451 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169537 | CTGGCCCTGCACTTT[-/C]CCCTTAAAATGCACC | 7464 |
rs34187832 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147576 | AGATCGGTATCACCT[-/G]GGGAGGAGGGAAGTC | 7464 |
rs34219253 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181562 | GTAAACGTGAGCAGA[-/C]CCCTCGGCGGCCATT | 7464 |
rs34341064 | in-del | -/A | 0.251296 | 0.249997 | intron-variant | CORO2A | GRCh38.p7 | 9:98148810 | ACACACACAAAACAC[-/A]AAAAAAAATGATCAA | 7464 |
rs34374919 | in-del | -/C | 0.110872 | 0.20771 | intron-variant | CORO2A | GRCh38.p7 | 9:98137830 | GCCTTACTTCTTATT[-/C]CCTGTGGGATCCTGG | 7464 |
rs34397649 | in-del | -/A/ACAA/ACACAA/ACACAC/C | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98158860 | CACACACACACACAC[-/A/ACAA/ACACAA/ACACAC/C]CATGTATATTGGGTA | 7464 |
rs34480810 | in-del | -/A | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123357 | AGCTTTCAAACTTCT[-/A]AAAAAATTTTTTTTT | 7464 |
rs34513364 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176302 | AAATCATATTACATC[-/T]TAGGGGTAAGCACCA | 7464 |
rs34545711 | snp | A/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121448 | GATGGTTTAAAAAAA[A/T]ATCTGATAAAAATTA | 7464 |
rs34601630 | in-del | -/A | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98189890 | GCAACTCCTTTATTT[-/A]TTTTTTTTTTTTGAG | 7464 |
rs34615679 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177988 | AGCTGATGAAGTGAC[-/T]TGCAATAGAAACCCC | 7464 |
rs34704909 | in-del | -/CAAA | 0.394721 | 0.203852 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194287 | AGTGGGACTCTGTCT[-/CAAA]CAAACAAACAAACAA | 7464 |
rs34709283 | snp | C/T | 0.139903 | 0.224452 | intron-variant | CORO2A | GRCh38.p7 | 9:98148338 | AGGCGGAGGCTTCAG[C/T]GAGCCAATATCATGC | 7464 |
rs34718287 | snp | G/T | 0.28578 | 0.247426 | intron-variant | CORO2A | GRCh38.p7 | 9:98147456 | TCTGGGCTGAGGAAA[G/T]TTCATCATATTATTT | 7464 |
rs34740598 | in-del | -/T | 0.355096 | 0.226837 | intron-variant | CORO2A | GRCh38.p7 | 9:98155343 | ATTTTTATTGCTCAA[-/T]TTTTTTTTTTTTTTT | 7464 |
rs34779636 | in-del | -/A | 0.423726 | 0.179776 | intron-variant | CORO2A | GRCh38.p7 | 9:98148395 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs34900554 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184576 | ACAGTGCTCCCGTCC[-/T]TCTATCCCTATCCCT | 7464 |
rs34999122 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98169435 | CCCCACGGCCCCCAC[C/T]TGCTCTCTACCCCTC | 7464 |
rs35088229 | in-del | -/G | 0.292523 | 0.246357 | intron-variant | CORO2A | GRCh38.p7 | 9:98148530 | GATCACTTAAGCCCA[-/G]GGGGTTCAAGACCAA | 7464 |
rs35123837 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138411 | GTGAAACTATGTCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs35149366 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150564 | GGTCCCCTCTCCCAA[-/C]ACCACGTCACACTCT | 7464 |
rs35180090 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140394 | AGGGAACACCCAACC[-/T]TTCTCTTCTTCCATC | 7464 |
rs35239999 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157297 | GACAGGTGTATTTTT[-/C]CCCAGTGAGGAAACC | 7464 |
rs35306686 | in-del | -/CA | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98149951 | TTTTTTTTTTTGAGA[-/CA]GAGTCTCGCACTGTT | 7464 |
rs35341581 | in-del | -/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174008 | TAATCCCAGCTACTC[-/G]GGGAGGGAGAATTGC | 7464 |
rs35394733 | in-del | -/A | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98166945 | GAAATAAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 7464 |
rs35411196 | in-del | -/AA | 0.326506 | 0.238006 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187475 | AAAAAAAAAAAAAAA[-/AA]TGTAGGTGCTTTATC | 7464 |
rs35462934 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165878 | TGAATCAGGTATTCT[-/G]GGGGGTGGGGCTCAC | 7464 |
rs35480968 | snp | A/G | 0.369346 | 0.219673 | intron-variant | CORO2A | GRCh38.p7 | 9:98178800 | CATAGATCACTTTGG[A/G]GGCAATTGGGATAGA | 7464 |
rs35490358 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | CORO2A | GRCh38.p7 | 9:98139279 | TGAACTATACACCTT[-/A]AAAACGGTGAATTTT | 7464 |
rs35559803 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149653 | GAACTCATTATCACA[-/G]GGGAGGGCATCAAGC | 7464 |
rs35576530 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160794 | CCCCTCATGTCCAGG[-/C]CCCTTCCAGTCAGGC | 7464 |
rs35581733 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167104 | GCAAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs35687148 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138120 | GGTCTATCTCCATGG[-/T]AAAATGAAAAGATAA | 7464 |
rs35737296 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98132836 | TCATTTCATCTCTCA[C/T]GGGCCTCAGTTTTCT | 7464 |
rs35748028 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170481 | AGTCTCGCTCTGTCA[-/C]CCCAGGCTGGAGTGC | 7464 |
rs35758963 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141298 | GCTAGGGTCTTAGAA[-/G]GGACACTGCACCCAC | 7464 |
rs35787916 | snp | A/C | 0.0475907 | 0.146733 | missense | CORO2A | GRCh38.p7 | 9:98124868 | AGCTCCCGGAGCCTT[A/C]GGATCTCCTCCTGTT | 7464 |
rs35878197 | snp | C/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98145684 | GTGGACACACATCGG[C/G]TTGAGAAGGGTCAGG | 7464 |
rs35894929 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160305 | AAAATAGGGACACAA[-/G]GGAAAATGCAGGTAA | 7464 |
rs35905939 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158709 | AGTGACTTGGAGGAT[-/G]GAGTAGGAGTTGGTC | 7464 |
rs35942540 | in-del | -/G/GG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160545 | AGAGAAATGGGTACT[-/G/GG]GGGGGTCCCCTTGGA | 7464 |
rs36010031 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170293 | CCCTGTGGGTACCCA[-/G]GGGGGAGGCCAACCT | 7464 |
rs36118702 | in-del | -/C | | | frameshift-variant | CORO2A | GRCh38.p7 | 9:98124864 | CAACAGCTCCCGGAG[-/C]CTTCGGATCTCCTCC | 7464 |
rs36159110 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187204 | GGGGAATAGCATGAA[-/C]CCCGGGAGGTGGAGC | 7464 |
rs41274266 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123225 | CCCAAAAGAGCAAAA[A/G]GACAGACCCAGAAAA | 7464 |
rs41274268 | snp | C/T | 0.0185938 | 0.0946107 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124638 | CACTGGAATCTCTTT[C/T]AGCGATGGAGAGTTT | 7464 |
rs41274270 | snp | C/T | 0.00302518 | 0.0387742 | intron-variant | CORO2A | GRCh38.p7 | 9:98131108 | TCACTCCTGGGGGCC[C/T]TCAGTGGTGCTCCCG | 7464 |
rs41313315 | snp | C/T | 0.338976 | 0.23363 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122244 | CATGCAGTCTTCCAT[C/T]TTCACTGTACTGCAG | 7464 |
rs41409644 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98169617 | TCAAAGACTCAGGGG[A/G]AACGTAGGGACCTCA | 7464 |
rs45442996 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122472 | GCAATGGAGATCATC[C/T]GCCCCTCCTTGGTAA | 7464 |
rs45514293 | snp | A/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121424 | AACAAAAATGTAATT[A/T]AAAAAACAGATGGTT | 7464 |
rs55635628 | snp | C/T | 0.205417 | 0.245993 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123356 | TAGCTTTCAAACTTC[C/T]AAAAAAATTTTTTTT | 7464 |
rs55644517 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98140959 | TATCACAACATTAAA[C/T]TTATATAAGTTGATA | 7464 |
rs55645026 | in-del | -/AACA | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194309 | ACAAACAAACAAACA[-/AACA]TATGGATGAAATCAG | 7464 |
rs55685018 | in-del | -/AC/ACAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153693 | CACACACACACACAC[-/AC/ACAC]TCACACACACACCCC | 7464 |
rs55701015 | snp | C/G | 0.100588 | 0.200439 | intron-variant | CORO2A | GRCh38.p7 | 9:98179019 | CTAAAAGTGGTCACA[C/G]TCTAGCTCTTTACCG | 7464 |
rs55710345 | snp | G/T | 0.178465 | 0.239547 | intron-variant | CORO2A | GRCh38.p7 | 9:98188407 | GTAAGCTCTTTGGGG[G/T]AAGATCTTTCTGGTC | 7464 |
rs55736211 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | CORO2A | GRCh38.p7 | 9:98138731 | TGGTACCTGGTATCT[A/G]GAACCCTAAGTAATG | 7464 |
rs55744221 | snp | G/T | 0.110872 | 0.20771 | intron-variant | CORO2A | GRCh38.p7 | 9:98176604 | TGGCTCCACTGGGGG[G/T]TGGGGGTTTCTTGTG | 7464 |
rs55752813 | snp | C/T | 0.354881 | 0.226936 | intron-variant | CORO2A | GRCh38.p7 | 9:98184622 | TCTACAGGGACGTAG[C/T]GCTTTGGGTCTGACG | 7464 |
rs55763078 | in-del | -/T | 0.441158 | 0.161117 | intron-variant | CORO2A | GRCh38.p7 | 9:98184233 | AATTATTTTATTTTA[-/T]TTTTTTTTTTAATAG | 7464 |
rs55835454 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98170043 | ATTTGTCTCTGTGCC[A/G]TAGCATTAGAGTATC | 7464 |
rs56020859 | snp | C/T | 0.172351 | 0.237636 | intron-variant | CORO2A | GRCh38.p7 | 9:98167940 | TCATTTGAATCTTTC[C/T]TTTAATTTTGTATGT | 7464 |
rs56157131 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98170176 | CCCTCGTCTCCTTTC[C/G]TGCCCACTGTGTTTT | 7464 |
rs56274862 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | CORO2A | GRCh38.p7 | 9:98175419 | ATTAGCACCAACTCC[A/C]ACTGGGCTTCAGCAG | 7464 |
rs56288207 | snp | A/G | 0.142947 | 0.22592 | intron-variant | CORO2A | GRCh38.p7 | 9:98171564 | AGGGCTAAAGCCAGC[A/G]CTGCAAGTTGCAGCA | 7464 |
rs56316923 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151947 | TCAGCCTCCCATGTA[A/G]CTGGGACCACAGGCG | 7464 |
rs56350443 | snp | C/T | 0.170733 | 0.237101 | intron-variant | CORO2A | GRCh38.p7 | 9:98185158 | CTCTAGGGAGCCTTC[C/T]ATGACCCCCCACTTC | 7464 |
rs56358945 | snp | C/T | 0.355311 | 0.226737 | intron-variant | CORO2A | GRCh38.p7 | 9:98184605 | CTGGCAGGTCCCAGG[C/T]CTCTACAGGGACGTA | 7464 |
rs56675709 | snp | C/T | 0.178465 | 0.239547 | intron-variant | CORO2A | GRCh38.p7 | 9:98185355 | TGGGGTGAAGATCAT[C/T]ACAATGACTAAGGCA | 7464 |
rs56735263 | snp | A/T | 0.254664 | 0.249956 | intron-variant | CORO2A | GRCh38.p7 | 9:98161546 | GGAACAGAGTGATAA[A/T]CTGTCTCAAAAATAA | 7464 |
rs56798255 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131765 | AAATGCTCCCTCAAA[-/A]TACTACCGCCAGCTT | 7464 |
rs56916178 | snp | C/T | 0.205723 | 0.246048 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174697 | TTCCCCTGCGAGTTA[C/T]CTCCCTCCTGCAGCC | 7464 |
rs56931336 | in-del | -/TG/TTG/TTT | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98156068 | TTTTTTTTTTTTTTT[-/TG/TTG/TTT]GAGACAGGGTCTCAC | 7464 |
rs57077760 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187474 | AAAAAAAAAAAAAAA[-/AAA]TGTAGGTGCTTTATC | 7464 |
rs57753377 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179861 | TACAAAAATTAGCCA[C/G]GTGCGGTGGCAGGTG | 7464 |
rs57756870 | snp | C/T | 0.181869 | 0.243788 | intron-variant | CORO2A | GRCh38.p7 | 9:98185101 | CCTTCATAGTCTGGC[C/T]GTCTCCAAATCACAC | 7464 |
rs57761120 | snp | A/G | 0.125528 | 0.21681 | intron-variant | CORO2A | GRCh38.p7 | 9:98185037 | AATGAAGAAACTGAC[A/G]CTTAGAGAAGTGGAG | 7464 |
rs57830760 | snp | A/G | 0.146314 | 0.227484 | intron-variant | CORO2A | GRCh38.p7 | 9:98174997 | AAGAAAAGAGAAATG[A/G]CAGCACTTAGGTATC | 7464 |
rs58069841 | snp | A/G | 0.439363 | 0.163222 | intron-variant | CORO2A | GRCh38.p7 | 9:98184768 | ATCAAGGGGTGTGTG[A/G]TTAATGGCGGCTGTC | 7464 |
rs58097113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98139621 | AATAGAGTGAGACTC[C/T]GTCTCAAAAATAAAT | 7464 |
rs58302299 | snp | A/T | 0.178465 | 0.239547 | intron-variant | CORO2A | GRCh38.p7 | 9:98188470 | CCCCAGCACTTAGAA[A/T]ATACCTAGTACAGGT | 7464 |
rs58330261 | in-del | -/A | 0.435407 | 0.167703 | intron-variant | CORO2A | GRCh38.p7 | 9:98158281 | TGAGACCCTGTCTCT[-/A]AAAAAAAAATAAAAG | 7464 |
rs58395439 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167119 | AAAAAAAAAAAAAAA[-/AAA]GAAAGAAAAGAAAAA | 7464 |
rs58652900 | snp | C/T | 0.150333 | 0.229274 | intron-variant | CORO2A | GRCh38.p7 | 9:98152219 | TGTTTCTACTTGAAT[C/T]GGTATTGACAAGTTA | 7464 |
rs58780438 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177757 | AAGAAAAAAAAAAAA[-/A]CAAACTGTGCTCACA | 7464 |
rs58907201 | snp | C/G | 0.011183 | 0.0739353 | intron-variant | CORO2A | GRCh38.p7 | 9:98132337 | GGTATTGGAGAGACA[C/G]TAGAGGATCGGGGGC | 7464 |
rs58978360 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148410 | AAAAAAAAAAAAAAA[-/A]TAAGATAAATAAATA | 7464 |
rs59025844 | snp | A/T | 0.354235 | 0.227234 | intron-variant | CORO2A | GRCh38.p7 | 9:98184770 | CAAGGGGTGTGTGGT[A/T]AATGGCGGCTGTCTG | 7464 |
rs59101768 | snp | A/G | 0.122758 | 0.215196 | intron-variant | CORO2A | GRCh38.p7 | 9:98181404 | TGGTCTGGAACTCCT[A/G]GCTTCAAGCAATCCT | 7464 |
rs59104692 | snp | C/G | 0.067446 | 0.170804 | intron-variant | CORO2A | GRCh38.p7 | 9:98134399 | TGAACAGGGTTCCCC[C/G]CAAAACTCATGTCCA | 7464 |
rs59146542 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138426 | AAAAAAAAAAAAAAA[-/A]GAAACTGGTTCACCA | 7464 |
rs59549202 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148410 | AAAAAAAAAAAAAAA[-/A]TAAGATAAATAAATA | 7464 |
rs59604725 | snp | C/T | 0.247905 | 0.249991 | intron-variant | CORO2A | GRCh38.p7 | 9:98188217 | TCCTTCAAGCCTTTG[C/T]CTAAAAATCACCTTC | 7464 |
rs60119235 | in-del | -/AAGA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163771 | AGAGAGAGAGAGAGA[-/AAGA]GAGAAAGAGACAGAG | 7464 |
rs60227744 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | CORO2A | GRCh38.p7 | 9:98129300 | CGCTCCAGATTCCTT[C/T]TGAGTAGGGTTAGCA | 7464 |
rs60243944 | in-del | -/ACAAAACAAAACAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148773 | ACAAAACAAAACAAA[-/ACAAAACAAAACAAA]CAAACAAAAAAAACA | 7464 |
rs60244725 | snp | C/T | 0.119281 | 0.213102 | intron-variant | CORO2A | GRCh38.p7 | 9:98160015 | TCAGGCAAGTCATAG[C/T]GATAAGGGCCTGACC | 7464 |
rs60290184 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187308 | AAAAAAAAAAAAAAA[-/AA]TTAGCCAGGCATGAT | 7464 |
rs60302015 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131345 | TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTAAC | 7464 |
rs60338078 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98156763 | GTGGATTCATATTTC[C/T]CTATGTTTAATCTGT | 7464 |
rs60542260 | in-del | -/T | 0.441841 | 0.160303 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121422 | TAAACAAAAATGTAA[-/T]TTAAAAAACAGATGG | 7464 |
rs60563416 | in-del | -/TGT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163742 | GTATGTGTGTGTGTG[-/TGT]AGAGAGAGAGAGAGA | 7464 |
rs60626374 | snp | A/G | 0.118235 | 0.212457 | intron-variant | CORO2A | GRCh38.p7 | 9:98176707 | ACTCGAACTCTGCAG[A/G]TGGGGGCTGAGAACT | 7464 |
rs60944850 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98159981 | TCAATTCCTCAGAAC[A/G]AGATTACACTGTGTG | 7464 |
rs61002365 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185587 | TACCTGGTCAGCCAG[C/G]TGTGAAAGGGAGGTT | 7464 |
rs61074100 | snp | A/C | 0.364401 | 0.222289 | intron-variant | CORO2A | GRCh38.p7 | 9:98158150 | TAAAATGAGGTAACA[A/C]AAGTATCCATCTCAG | 7464 |
rs61080625 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CORO2A | GRCh38.p7 | 9:98135894 | ACTGCATAGAACCCC[A/G]GGAGGAAGACACACT | 7464 |
rs61124973 | in-del | -/TGTGTGTGTGTGT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163743 | TATGTGTGTGTGTGA[-/TGTGTGTGTGTGT]GAGAGAGAGAGAGAG | 7464 |
rs61182322 | snp | G/T | 0.493293 | 0.0575177 | intron-variant | CORO2A | GRCh38.p7 | 9:98188494 | TACAGGTCAGGTGTG[G/T]TGGCTCACATCTGTA | 7464 |
rs61262808 | in-del | -/T | 0.34437 | 0.231505 | intron-variant | CORO2A | GRCh38.p7 | 9:98156068 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 7464 |
rs61282671 | snp | A/G | 0.107694 | 0.205546 | intron-variant | CORO2A | GRCh38.p7 | 9:98154127 | TGAGTGAGATTGATC[A/G]ATATTTTTTTCTTTC | 7464 |
rs61513961 | in-del | -/ACACAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153688 | CACACACACACACAC[-/ACACAC]TCACACACACACCCC | 7464 |
rs61617506 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127844 | AAAAAAAAAAAAAAA[-/AA]GAATTGCAGAGGTAG | 7464 |
rs61741701 | snp | C/T | 0.00195935 | 0.0312383 | missense | CORO2A | GRCh38.p7 | 9:98157552 | CACAGAAGTGGTTGT[C/T]GTGAACGCTGCGGGT | 7464 |
rs62575607 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98148392 | AGAGCGAGACTCCAT[A/C]TCAAAAAAAAAAAAA | 7464 |
rs62575628 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CORO2A | GRCh38.p7 | 9:98164000 | ATGGGTAGGCATTGC[C/T]GGCTACCAGTGCCCC | 7464 |
rs62575629 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179878 | TGCGGTGGCAGGTGC[C/T]TGTAATCCCAGCTAC | 7464 |
rs62575630 | snp | C/G | 0.168135 | 0.236216 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193160 | GAGGAGAGGAGCCGG[C/G]AGCGCCGCTGGGAAC | 7464 |
rs66488824 | multinucleotide-polymorphism | CAC/TAT | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98154329 | ATATATATATATATA[CAC/TAT]ACACAAACACATAAG | 7464 |
rs66503728 | in-del | -/A | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98155364 | GCCAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs67277620 | in-del | -/GT | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98153658 | GGGGTGTGTGTGTGA[-/GT]GTGTGTGTGTGTGTG | 7464 |
rs71308246 | in-del | -/TGGTACAT | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98165119 | ATTAGCCAAGCACGG[-/TGGTACAT]TGGTACATGCTTGTT | 7464 |
rs71308247 | in-del | -/AT | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98154376 | ATACATATATTTAAA[-/AT]ATATATATATATATG | 7464 |
rs71308248 | in-del | -/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98139283 | TTGGAAAATTCACCG[-/T]TTTTAAGGTGTATAG | 7464 |
rs71369555 | in-del | -/TGTATATATATATATATATATA | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98154353 | ATATATGTATTTGTG[-/TGTATATATATATATATATATA]TATATATATATATAT | 7464 |
rs71494011 | multinucleotide-polymorphism | ACACACACACACATAC/TCTCACACACACACAT | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98163730 | CTCTCTCTCTCTCTC[lengthTooLong]ACACACACACACACA | 7464 |
rs71496888 | in-del | -/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98145848 | CTCCCAAGTAGCTGG[-/G]ACTACAGGCATGTGC | 7464 |
rs71501845 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98135017 | GGCACCGTCACCAGC[A/C]TAAGCCACAGATCTG | 7464 |
rs71501846 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98155840 | TCTGCTGTGATATTG[G/T]TTTTCTCATTCCTGA | 7464 |
rs71501847 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98176889 | CCAGGTCTCCAGCCT[C/T]CCAGTCCAAAAGAGT | 7464 |
rs71501848 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98177458 | GGGCTCCAAACTTTG[G/T]TTTTTTTTTTTTTTT | 7464 |
rs72256502 | in-del | -/GT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163712 | TGACATACATGCGGG[-/GT]GTGTGTGTGTGTGTG | 7464 |
rs72321582 | in-del | -/CTC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164941 | GTCACTCTCCCACCA[-/CTC]CTACCACCACCACCA | 7464 |
rs72327744 | in-del | -/C | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123496 | CTATTCTCTCTCTCT[-/C]TTTTTTTTTTTTTTT | 7464 |
rs72603681 | snp | A/G | 0.379158 | 0.214052 | intron-variant | CORO2A | GRCh38.p7 | 9:98165122 | CAAGCATGTACCACC[A/G]TGCTTGGCTAATTTT | 7464 |
rs72603682 | snp | C/T | 0.165853 | 0.235413 | intron-variant | CORO2A | GRCh38.p7 | 9:98168133 | AAATTAAATAAAGTG[C/T]AAAATCCAGCTCCTT | 7464 |
rs72603683 | snp | A/C | 0.144756 | 0.227146 | intron-variant | CORO2A | GRCh38.p7 | 9:98171972 | GAAACGATTTCTTTC[A/C]TCAACTTTGGGCTGG | 7464 |
rs72603684 | snp | A/C | 0.143622 | 0.226238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172053 | CTGGAGGGGTTGCGG[A/C]ACCCCATGAGGAGGA | 7464 |
rs72603685 | snp | C/T | 0.108755 | 0.206276 | intron-variant | CORO2A | GRCh38.p7 | 9:98178201 | ACAGGCATGAGCCAC[C/T]ATGCCCGGCTAATTA | 7464 |
rs72603686 | snp | C/T | 0.112631 | 0.208878 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185706 | CCCAGTTATTGAGCA[C/T]GCCATAGACCACGCC | 7464 |
rs72755479 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98143040 | CCACCTTCTGCCCAT[C/T]AGGCCAGCACTCAGC | 7464 |
rs72755490 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98151267 | AATAGGCTTGGAATA[C/T]GTCCTAAAAAAAGAG | 7464 |
rs72757935 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98177754 | CCACAAGAAAAAAAA[A/C]AAACAAACTGTGCTC | 7464 |
rs72757943 | snp | A/T | 0.0513262 | 0.151752 | intron-variant | CORO2A | GRCh38.p7 | 9:98180721 | ACCTCCAGCCTCCTG[A/T]CACCTGCCACATGTG | 7464 |
rs72757946 | snp | A/G | 0.207864 | 0.246424 | intron-variant | CORO2A | GRCh38.p7 | 9:98181179 | TGCTTGTGTCCCCCA[A/G]CGCGACTCCCTCTGC | 7464 |
rs72757947 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98181357 | TTTTTTTTTTTTTTT[C/T]AAGAGATGAGGTCTC | 7464 |
rs72757961 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98191014 | TTCTGCTTGAATACC[G/T]GTGATGACAAAGAGC | 7464 |
rs73498748 | snp | C/T | 0.141934 | 0.225437 | intron-variant | CORO2A | GRCh38.p7 | 9:98161006 | GTCCCTCAGGAACCA[C/T]GTGTAGCAGAGCACT | 7464 |
rs73498751 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CORO2A | GRCh38.p7 | 9:98164238 | TCAGGATAAAGAACG[C/T]TCTATGTGAAGGTGC | 7464 |
rs73498755 | snp | A/C | 0.0807149 | 0.183963 | intron-variant | CORO2A | GRCh38.p7 | 9:98165121 | ACAAGCATGTACCAC[A/C]GTGCTTGGCTAATTT | 7464 |
rs73498763 | snp | A/G | 0.140242 | 0.224618 | intron-variant | CORO2A | GRCh38.p7 | 9:98167083 | TACTCCAGTCTGGGT[A/G]ATAAAGCAAGATCCT | 7464 |
rs73498778 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | CORO2A | GRCh38.p7 | 9:98178056 | ATTTTTATTAAAAAC[A/T]TTTTTTTAGAGACAG | 7464 |
rs73498781 | snp | C/T | 0.16846 | 0.236329 | intron-variant | CORO2A | GRCh38.p7 | 9:98182037 | CTTTTGCAGTGACCC[C/T]GGACTCAGCACATTC | 7464 |
rs73498784 | snp | C/T | 0.171057 | 0.237209 | intron-variant | CORO2A | GRCh38.p7 | 9:98182064 | ATTCTCTACTCTGCA[C/T]GCCCTTCACTCCTCT | 7464 |
rs73503027 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | CORO2A | GRCh38.p7 | 9:98189530 | TAATGAATCTCCTTC[C/T]AATCTCGGCTTTGCT | 7464 |
rs73503029 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | CORO2A | GRCh38.p7 | 9:98191105 | GGGCAGGTCATGAAG[C/G]GGACAAGAAAGACCA | 7464 |
rs73503030 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | CORO2A | GRCh38.p7 | 9:98191708 | CACAGTCCCTCAGAC[C/T]TGTGCTCTGCCCCAT | 7464 |
rs73503038 | snp | A/C | 0.193653 | 0.243567 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193600 | TCCGTGGCACATAGT[A/C]ACCACTCAATATATA | 7464 |
rs73655193 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CORO2A | GRCh38.p7 | 9:98127333 | TACACCAGGAGGCCC[A/G]CTCAGCCACTGGGGT | 7464 |
rs73655194 | snp | A/C/G | 0.000971745 | 0.0220216 | missense | CORO2A | GRCh38.p7 | 9:98128672 | TCAGCTTGTAGAAGC[A/C/G]GAAGATCTCGCAGGA | 7464 |
rs73655195 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98134306 | CTGCCTGCATGCTTG[A/G]TTGTCAGTGGAGCAG | 7464 |
rs73655196 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CORO2A | GRCh38.p7 | 9:98135621 | GTAAGCTCCCTGTCA[C/T]AGAGGTATACAAATG | 7464 |
rs73655197 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | CORO2A | GRCh38.p7 | 9:98135774 | ACGACTTTGCTTTCA[A/C]TTCAGCAAATATTTA | 7464 |
rs73655198 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | CORO2A | GRCh38.p7 | 9:98144462 | ATGGTTATCATCATC[A/T]TCATACAGGCCTTTC | 7464 |
rs73655199 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CORO2A | GRCh38.p7 | 9:98145201 | TCACCTGTGGGGACA[A/G]GGAGCTCACTTCCTC | 7464 |
rs73655200 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CORO2A | GRCh38.p7 | 9:98145494 | ATGCCAGACTAGCCC[A/G]TACCCTGCCTTTCTA | 7464 |
rs73655201 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | CORO2A | GRCh38.p7 | 9:98147768 | TGACTCAGCAACCGC[A/T]CTCCTGGCCCTTTAT | 7464 |
rs73655202 | snp | C/T | 0.134119 | 0.221521 | intron-variant | CORO2A | GRCh38.p7 | 9:98154228 | TTCATCTTTTTTATT[C/T]GTGGAAATGTTTGTA | 7464 |
rs73657103 | snp | A/C | 0.148661 | 0.22854 | intron-variant | CORO2A | GRCh38.p7 | 9:98154381 | TATATATATATTTTA[A/C]ATATATGTATGTAAA | 7464 |
rs73657104 | snp | A/G | 0.101301 | 0.200969 | intron-variant | CORO2A | GRCh38.p7 | 9:98158015 | CAGTACCCTCAGCCC[A/G]ACTAAGTAGGTACCA | 7464 |
rs73657105 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98160550 | AAATGGGTACTGGGG[A/G]TCCCCTTGGAAAGAA | 7464 |
rs73657106 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98160667 | CAAGGAGCAAATCAG[C/G]AGGCTCCGCTCCAGG | 7464 |
rs73657107 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | CORO2A | GRCh38.p7 | 9:98160874 | TGGGAGGCAGTGATG[C/T]GTGTCACTTCCAGGC | 7464 |
rs73657108 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CORO2A | GRCh38.p7 | 9:98161849 | CTGGCCCCTTCCGGA[C/T]CCTCTGAGCTGTCTC | 7464 |
rs73657109 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | CORO2A | GRCh38.p7 | 9:98167892 | AAACAGGCTGCTGAT[C/G]GCTACTGAAAGTGGG | 7464 |
rs73657110 | snp | A/G | 0.190833 | 0.242898 | intron-variant | CORO2A | GRCh38.p7 | 9:98171092 | TTTCGAGCGACAAGG[A/G]TCACTGGGGATTTTC | 7464 |
rs73657111 | snp | A/G | 0.190833 | 0.242898 | intron-variant | CORO2A | GRCh38.p7 | 9:98171101 | ACAAGGATCACTGGG[A/G]ATTTTCCAAGACACC | 7464 |
rs73657112 | snp | A/G | 0.117537 | 0.212022 | intron-variant | CORO2A | GRCh38.p7 | 9:98172145 | GGACAAGAGTCCCCA[A/G]ATATGACTGAAGGCC | 7464 |
rs73657113 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO2A | GRCh38.p7 | 9:98178419 | CACAATTTTTCAGTA[C/T]GAATCTTTAAAAACC | 7464 |
rs74306837 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98163730 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGAGA | 7464 |
rs74387444 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98141860 | ATGAAGAGCCCAACA[A/G]TCAGGTGTTACTGTA | 7464 |
rs74393261 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98140123 | CCCTCGACCTCCCAC[A/G]TCCACCATCTAGTTC | 7464 |
rs74418414 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | CORO2A | GRCh38.p7 | 9:98184556 | TGGTTTCTTCATGGC[A/G]GCCCCACAGTGCTCC | 7464 |
rs74519906 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CORO2A | GRCh38.p7 | 9:98145686 | GGACACACATCGGCT[C/T]GAGAAGGGTCAGGTT | 7464 |
rs74528222 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | CORO2A | GRCh38.p7 | 9:98181539 | TGCCCTTGATCTTTC[C/T]GAAATATGTAAACGT | 7464 |
rs74563327 | snp | C/G | 0.0995161 | 0.199636 | intron-variant | CORO2A | GRCh38.p7 | 9:98162919 | TGGGCCAGAACAGCC[C/G]ATTCGAGCCAGGTCT | 7464 |
rs74567058 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173532 | GGCTCTGCTCCTTGG[C/T]TTGCTTTCTTAAGTC | 7464 |
rs74627629 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98152504 | TATGTTGCTGGTCTC[A/G]AACTCCTGGGCTCAA | 7464 |
rs74737086 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CORO2A | GRCh38.p7 | 9:98150633 | AGTACCCATTTACAC[C/T]GAGCAGTTCATGCAA | 7464 |
rs74774809 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98148786 | AAACAAACAAAAAAA[A/C]CAAAACACACACACA | 7464 |
rs74787267 | snp | C/T | 0.0726307 | 0.176182 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187670 | ATAAGAACACTAATC[C/T]CATTATGAGGGCTCT | 7464 |
rs74789058 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98133905 | ACTACTTGACGCATT[C/T]TCCCACACCTGGCTA | 7464 |
rs74817719 | snp | C/T | 0.217551 | 0.247885 | intron-variant | CORO2A | GRCh38.p7 | 9:98178705 | TGGCGAGTGTGTCTC[C/T]ACCTGGCAAATGTGA | 7464 |
rs74819986 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98192148 | AGCCAAGAGGGGGAG[A/G]GTCCCGACAAGAGTC | 7464 |
rs74833828 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98125442 | TCTGGGTCTAAGACC[C/T]TAAATTAGTACTCAG | 7464 |
rs74842144 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98144208 | AAAAAAAAAAAAAAA[A/G]CTTTTCTTTAGAAAC | 7464 |
rs74853643 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98156066 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGGGTCTC | 7464 |
rs74943592 | snp | G/T | 0.00872364 | 0.0654654 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157472 | TACCTGGTGCAGGGG[G/T]ATGACGAGGAAGGCC | 7464 |
rs74998744 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | CORO2A | GRCh38.p7 | 9:98182236 | CAAAGGTCCTAGTCA[A/C]AAAATTACATTGAAA | 7464 |
rs75122665 | snp | A/G | 0.431325 | 0.172108 | intron-variant | CORO2A | GRCh38.p7 | 9:98183176 | CAGAAAGCGGCCCAA[A/G]CTTCAGCAGGACCCT | 7464 |
rs75127405 | snp | A/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98153422 | TTTTTTTTTTTTTTT[A/T]TAAGAGATGGGGTCT | 7464 |
rs75264515 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98180792 | AACAGGTTCAGGCTC[A/G]AGTAGAGGGCCCTGG | 7464 |
rs75310823 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98145441 | GTATGTTCTTGTCCA[C/G]GATGAACAAACCCCT | 7464 |
rs75363862 | snp | C/G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98165911 | CTCTGCTTTAACCAG[C/G/T]CCCCCAGGTTCAAGT | 7464 |
rs75395775 | snp | A/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98163745 | ATGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAGAG | 7464 |
rs75635996 | snp | A/G | 0.216649 | 0.247765 | intron-variant | CORO2A | GRCh38.p7 | 9:98178236 | ACTTTTCCTTGAGGC[A/G]GGGATTTGCTATGTT | 7464 |
rs75670920 | snp | G/T | 0.176861 | 0.239062 | intron-variant | CORO2A | GRCh38.p7 | 9:98165241 | TGGGATGACAGGCGT[G/T]AGCCACCGTGCCTGG | 7464 |
rs75772867 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | CORO2A | GRCh38.p7 | 9:98174930 | TATACTTAAAAATGG[A/T]TAAAATCGTAAACTT | 7464 |
rs75773291 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | CORO2A | GRCh38.p7 | 9:98160670 | GGAGCAAATCAGCAG[G/T]CTCCGCTCCAGGCCC | 7464 |
rs75787358 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174664 | TCTCTTGAGATCTGA[C/T]GGTTTAAAAGTGGCA | 7464 |
rs75853958 | snp | A/C | 0.0861826 | 0.188849 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193832 | TGTACCACCCCCCTG[A/C]CCAGAGCTGGACGGG | 7464 |
rs75919093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98175046 | ACTCCCTGGCAGCTA[C/T]ATCTCTGCTTCCATG | 7464 |
rs76004754 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CORO2A | GRCh38.p7 | 9:98162090 | GAATAGAGCAAGTGG[G/T]TGCTACCTTGCTCCC | 7464 |
rs76064838 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148772 | AACAAAACAAAACAA[-/A]ACAAACAAAAAAAAC | 7464 |
rs76378338 | snp | G/T | 0.115438 | 0.210697 | intron-variant | CORO2A | GRCh38.p7 | 9:98133388 | GGCTGAAGCTGCTTG[G/T]GGCAGGAGGGGGAAT | 7464 |
rs76420829 | snp | C/G | 0.0865458 | 0.189163 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193348 | TCTGTGCATTACCTC[C/G]CTTCACTGTCACACA | 7464 |
rs76507727 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98163193 | CACTGAGTTTATTTC[C/T]TTTTTTTTCTTTGAG | 7464 |
rs76565201 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98133904 | GACTACTTGACGCAT[G/T]TTCCCACACCTGGCT | 7464 |
rs76578157 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154491 | GCTACCCTCCCAAGC[A/C]AAGACATGAACCATT | 7464 |
rs76679997 | snp | C/G | 0.0941369 | 0.195465 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193811 | GACTCAGCTTCCATA[C/G]TCCACTGTACCACCC | 7464 |
rs76727580 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98171153 | CAGCTCCACTCCCTG[C/T]TCACTGTCCGCTTTC | 7464 |
rs76790287 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | CORO2A | GRCh38.p7 | 9:98141173 | TGTTAGTGATGTGCA[C/T]GGAGGGAGGTGAAAA | 7464 |
rs76858557 | snp | C/T | 0.154329 | 0.23097 | intron-variant | CORO2A | GRCh38.p7 | 9:98183780 | GCCTGGCCAACATAG[C/T]GAAACCCCATCTCTA | 7464 |
rs76859928 | snp | C/G | 0.0876345 | 0.190099 | intron-variant | CORO2A | GRCh38.p7 | 9:98162080 | TTCCATGCATGAATA[C/G]AGCAAGTGGGTGCTA | 7464 |
rs76999408 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98147140 | AAGAAACATCAATCA[A/G]ATGCAAGATGTGGAC | 7464 |
rs77077101 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98138412 | GTGAAACTATGTCTC[A/C]AAAAAAAAAAAAAAG | 7464 |
rs77288058 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98158078 | CAATCCCAGCTCTGT[C/G]TCTTATCAGCTGGAT | 7464 |
rs77297972 | snp | A/C | 0.046775 | 0.145601 | intron-variant | CORO2A | GRCh38.p7 | 9:98169760 | AAGCATCATTTTCCC[A/C]GATAATCTGTCTTTG | 7464 |
rs77416773 | snp | A/G | 0.000742789 | 0.0192573 | missense | CORO2A | GRCh38.p7 | 9:98128202 | AGCCACTCCTGGGCC[A/G]TCAGGGAGGGCTGGG | 7464 |
rs77446196 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183175 | TCAGAAAGCGGCCCA[A/G]ACTTCAGCAGGACCC | 7464 |
rs77613317 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CORO2A | GRCh38.p7 | 9:98149890 | GAATCACACATTTTA[C/T]CTAGGATCAGGCTGT | 7464 |
rs77658502 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98184874 | TTTCCCTAACCCCTA[A/G]GGGCTCCAGAAATCA | 7464 |
rs77663336 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CORO2A | GRCh38.p7 | 9:98159500 | CACCTTCCAGCTTCC[C/T]CAGCACCTGCTCTTG | 7464 |
rs77687240 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | CORO2A | GRCh38.p7 | 9:98146332 | TGAGTACAGTCCCTG[G/T]TTGCCAAGGCTGCAG | 7464 |
rs77702835 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98149164 | ACTGTACTATTTCTT[A/G]TAACTGCTTGTGAAT | 7464 |
rs77832229 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98164946 | CTCTCCCACCACTAC[C/T]ACCACCACCAGGGTC | 7464 |
rs77947501 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98139971 | CTATTTCCAACTCCA[C/T]CAAGAGACTTGGATT | 7464 |
rs78007144 | snp | A/C/T | 0.00597678 | 0.0543977 | intron-variant | CORO2A | GRCh38.p7 | 9:98169180 | AAATGCAAAGAGTCC[A/C/T]GTCCTCAGGTTTCCG | 7464 |
rs78075956 | snp | C/T | 0.100944 | 0.200705 | intron-variant | CORO2A | GRCh38.p7 | 9:98149091 | TGCTGTACTGCGTAC[C/T]GTAGTCTTATAAGAT | 7464 |
rs78215685 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98138411 | AGTGAAACTATGTCT[A/C]AAAAAAAAAAAAAAA | 7464 |
rs78227510 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98171909 | GACATGGTCAGAGCC[A/G]AAATAGACTTAACCC | 7464 |
rs78348574 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98130081 | GGGATATTCATTTTA[C/T]TTTAGATTTTATCTT | 7464 |
rs78378660 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174149 | AAAAACAAAAAAAAA[-/AAA]CCAAAGAGCGTGTAG | 7464 |
rs78444735 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | CORO2A | GRCh38.p7 | 9:98135200 | TGACCAGGGATGAGT[C/T]TAGGCCTCCAAATCT | 7464 |
rs78486797 | snp | G/T | 0.0865458 | 0.189163 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193284 | AGGCCCTACCTTTGG[G/T]TACCACCCCCACCTA | 7464 |
rs78514102 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CORO2A | GRCh38.p7 | 9:98180695 | GCACCCCTCCTGACC[A/G]CACCCTCCCCACCTC | 7464 |
rs78629588 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CORO2A | GRCh38.p7 | 9:98152854 | TTAATATCATGAAGT[A/G]ATGAAGACTAAGAGA | 7464 |
rs78656811 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98139063 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAATGCAGA | 7464 |
rs78671911 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98144207 | GAAAAAAAAAAAAAA[A/G]GCTTTTCTTTAGAAA | 7464 |
rs78729264 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CORO2A | GRCh38.p7 | 9:98182524 | CACTGGAGCATTTCT[A/G]AGCTGGCATTGTGGA | 7464 |
rs78734129 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | CORO2A | GRCh38.p7 | 9:98178057 | TTTTTATTAAAAACA[C/T]TTTTTTAGAGACAGA | 7464 |
rs78774229 | snp | G/T | 0.0876345 | 0.190099 | intron-variant | CORO2A | GRCh38.p7 | 9:98162078 | CTTTCCATGCATGAA[G/T]AGAGCAAGTGGGTGC | 7464 |
rs78803401 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | CORO2A | GRCh38.p7 | 9:98130071 | GGGTGATGAGGGGAT[A/C]TTCATTTTATTTTAG | 7464 |
rs78879445 | snp | A/G | 0.00909942 | 0.0668349 | intron-variant | CORO2A | GRCh38.p7 | 9:98126853 | GAGCCATGTGAGGAC[A/G]GGGTGCCCACGGGAA | 7464 |
rs78900821 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98163732 | TGTGTGTGTGTGTAT[A/G]TGTGTGTGTGAGAGA | 7464 |
rs78901557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98174898 | ACAATGGGAATGTAC[A/G]TCATGCCACGGAATT | 7464 |
rs78980749 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98181460 | GGATTATAGGCGTGA[A/G]CCTCGGTGCCTGGCT | 7464 |
rs79085939 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CORO2A | GRCh38.p7 | 9:98161120 | GCGACCCATCCTGAT[A/T]CATACAGCCTATGCA | 7464 |
rs79100589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147740 | TTATAAGGCTAAACA[C/T]GCAACTACCTTATGA | 7464 |
rs79141746 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98152126 | CCGGCCTCTTTTGCT[G/T]TTTTTTTTTTTTGTT | 7464 |
rs79166425 | snp | C/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98159341 | GCGTGAGCCACTGCC[C/G]CTGGCCTCACATCAC | 7464 |
rs79283988 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98177005 | TAATAGTGGAAACTC[A/G]TTTGTGGAGGGACAA | 7464 |
rs79385917 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | CORO2A | GRCh38.p7 | 9:98167635 | TGGATCCGGATTCAC[A/G]CAAACCAATTGCAAA | 7464 |
rs79466601 | snp | C/G | 0.334412 | 0.235318 | intron-variant | CORO2A | GRCh38.p7 | 9:98181235 | CCGGAAAAGCCAGAA[C/G]CCACGGGCACCCACG | 7464 |
rs79490560 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | CORO2A | GRCh38.p7 | 9:98163160 | GAAAGGATGTAGTCA[C/T]CTCTGGGTTTTGCAT | 7464 |
rs79521415 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98183240 | GTGGTAGGTTCCACA[A/G]TTGGACAGTTTGGTC | 7464 |
rs79541363 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98126143 | CAATTTCAAGCCATT[C/T]TCCTGCCTCAACCTC | 7464 |
rs79565693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98127122 | TGCCCTTGCTTTGTA[A/G]GGACAGTCCCACCCA | 7464 |
rs79600003 | snp | C/T | 0.352938 | 0.227824 | intron-variant | CORO2A | GRCh38.p7 | 9:98179959 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 7464 |
rs79686889 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174715 | CTCTCCTGCCACCTT[A/G]TGAAGAAGGTACTTG | 7464 |
rs79692530 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | CORO2A | GRCh38.p7 | 9:98189123 | CCATTTAGGCTGAAC[C/G]AAATGAAATTGCCAT | 7464 |
rs79804230 | snp | C/T | 0.249038 | 0.249998 | intron-variant | CORO2A | GRCh38.p7 | 9:98167418 | TATGAGCGTACTTAA[C/T]ACCACTGAACTGTAC | 7464 |
rs79886267 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | CORO2A | GRCh38.p7 | 9:98140168 | ACCCACCAGAATGCT[C/T]CCCCAGCCATTTTTA | 7464 |
rs80054081 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | CORO2A | GRCh38.p7 | 9:98150561 | CTAGGTCCCCTCTCC[C/G]AACCCACGTCACACT | 7464 |
rs80207665 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98149342 | CCCACTTCAGACCCA[C/T]TACATCAGAATCTGT | 7464 |
rs80214852 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181232 | CTGCCGGAAAAGCCA[A/G]AACCCACGGGCACCC | 7464 |
rs80227567 | snp | C/T | 0.175576 | 0.238665 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192962 | GATGAGGAACCTGAC[C/T]TCCCGGAGCCTCAGT | 7464 |
rs80265650 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191044 | CTCACTACCTGTCCA[G/T]GGGCCTCCTGCCCTC | 7464 |
rs80277213 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | CORO2A | GRCh38.p7 | 9:98154051 | TCTGGAATAAATCCA[A/G]CTTGGTCAGAATGTA | 7464 |
rs80293000 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | CORO2A | GRCh38.p7 | 9:98168214 | TCACAGATGAAACCA[C/T]ACAAGCAACACCCAA | 7464 |
rs80330254 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98135760 | GGTTTTTCAGGTAGA[C/T]GACTTTGCTTTCAAT | 7464 |
rs111241578 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | CORO2A | GRCh38.p7 | 9:98192446 | AGGTCCCCCGCGCTC[C/G]GAGCCCCGCATCCCT | 7464 |
rs111300916 | in-del | -/CTT | 0.0659589 | 0.169201 | intron-variant | CORO2A | GRCh38.p7 | 9:98171065 | TTGCCCCACAATCTC[-/CTT]ATCTGGGAGTTTCGA | 7464 |
rs111305375 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98150363 | CTCCTCCCACCACTC[C/T]GTGGTCACAGCACAT | 7464 |
rs111314116 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98139515 | GCCTGTAATCCAAGC[G/T]ACTTGGGAGACTGAG | 7464 |
rs111332589 | snp | A/C | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98190469 | TTTTTTGGAGAAAAA[A/C]AGGCACTCCAATCTT | 7464 |
rs111407487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98143941 | GGCTGGGCACAGTGG[C/T]TCATGTCTGTAATTC | 7464 |
rs111443650 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | CORO2A | GRCh38.p7 | 9:98161423 | GCCGGGTGTGGTGGC[A/G]CGCGCCTGTAGTCCC | 7464 |
rs111467436 | in-del | -/T | 0.362941 | 0.223034 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124014 | AGGCTGGTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs111556785 | snp | C/T | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174523 | GGTGATATGGTTTGG[C/T]TCTGTGTCCCCACCC | 7464 |
rs111564137 | snp | A/G | 0.276534 | 0.248588 | intron-variant | CORO2A | GRCh38.p7 | 9:98127484 | AGAGGGACCTGGGTG[A/G]GGGTTGCTGCCTGGA | 7464 |
rs111592449 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO2A | GRCh38.p7 | 9:98180384 | CTTCCTGCAAGCATT[C/T]CCATCCATCCCCTCG | 7464 |
rs111659018 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98126280 | ACCTCATGATCTGCC[C/T]GCCTTGGCCTCCCAA | 7464 |
rs111664732 | in-del | -/A | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98184493 | TCTCATTCCACACAT[-/A]ACTACTCTTTCTCTT | 7464 |
rs111749402 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98145376 | ACATCTGGGCCCTCT[A/G]TGGCAGGCCAACTCC | 7464 |
rs111757914 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98126852 | AGAGCCATGTGAGGA[C/T]GGGGTGCCCACGGGA | 7464 |
rs111773326 | snp | A/C | 0.187053 | 0.241946 | intron-variant | CORO2A | GRCh38.p7 | 9:98153266 | TACCACACCTGGCTA[A/C]TTTTTTGTGTTTTTA | 7464 |
rs111806669 | snp | C/G/T | 0.0134861 | 0.0810011 | intron-variant | CORO2A | GRCh38.p7 | 9:98184653 | TTGTTCCTCCTCATC[C/G/T]TCAGAGTGGGGCTGT | 7464 |
rs111826257 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98171954 | TCAGGACATTGAGCC[C/T]GGGAAACGATTTCTT | 7464 |
rs111850348 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98177213 | CATCAGCAGCCCCCA[C/T]GATGTGAGGGGAAAC | 7464 |
rs111936255 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187139 | AAAAACAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 7464 |
rs111953206 | in-del | -/CTT | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98169637 | TGAGTCTTTGACCTC[-/CTT]CTCATCTCCACAGAC | 7464 |
rs111972208 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98147667 | TATTTTAGCATAAGG[A/C]GGTTCCATGCAATAT | 7464 |
rs112047739 | snp | A/G | 0.145642 | 0.227177 | utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98192633 | TCCTCGCCGCCCGCC[A/G]ACTCCCGGCGCCCAG | 7464 |
rs112052630 | snp | C/T | 0.193966 | 0.243639 | intron-variant | CORO2A | GRCh38.p7 | 9:98189915 | TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG | 7464 |
rs112090093 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123954 | ACCACCACGCCCTGC[C/T]TAATTTTTGTATTTT | 7464 |
rs112155106 | in-del | -/TGCCGGAA | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98181232 | TGCCGGAAAAGCCAG[-/TGCCGGAA]AACCCACGGGCACCC | 7464 |
rs112175052 | in-del | -/A | 0.43088 | 0.172575 | intron-variant | CORO2A | GRCh38.p7 | 9:98183174 | CTCAGAAAGCGGCCC[-/A]AACTTCAGCAGGACC | 7464 |
rs112179489 | in-del | -/T | 0.473174 | 0.112665 | intron-variant | CORO2A | GRCh38.p7 | 9:98131331 | CCCTTAACAAATCAC[-/T]TTTTTTTTTTTTTTG | 7464 |
rs112276721 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98132099 | TGTGTGTGTCATAAA[C/T]GGGTGTCTAAATGAA | 7464 |
rs112313589 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98175077 | TTGATTTCCACAGAG[A/C]TCCTATTCTTTTAGC | 7464 |
rs112352631 | snp | A/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98142560 | GGGCCATGCCCCAAT[A/T]TCCGCAGTGCGGTTT | 7464 |
rs112369691 | snp | A/C | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98151059 | TACAGTTGCACCTCC[A/C]TGCCTTTGCTTGTGC | 7464 |
rs112446672 | snp | A/G | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98137049 | GGTACAAAATGAATT[A/G]TAAATAAGTAACACT | 7464 |
rs112540774 | snp | G/T | 8.23676e-05 | 0.00641693 | missense | CORO2A | GRCh38.p7 | 9:98126609 | ATTTGTCAGCCAGGT[G/T]TTCTTCTCCTCCAGC | 7464 |
rs112547443 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174151 | GCCAAAACAAAAAAC[-/A]AAAAAAAAAAAACCA | 7464 |
rs112548191 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98139335 | CGTCTCTACAAAAAA[C/T]CAAAAAATTAGGCCT | 7464 |
rs112553109 | snp | C/T | 0.079617 | 0.182947 | intron-variant | CORO2A | GRCh38.p7 | 9:98178207 | ATGAGCCACCATGCC[C/T]GGCTAATTATTAAAC | 7464 |
rs112561237 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CORO2A | GRCh38.p7 | 9:98184658 | CCTCCTCATCCTCAG[A/C]GTGGGGCTGTGATCT | 7464 |
rs112577379 | in-del | -/A | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98125687 | GGTCAAACCCTCTCC[-/A]TTTTACAGATGGTTT | 7464 |
rs112629127 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98159543 | TCTGGCTCTTTGCCC[A/G]TCCCTCTCCTTCTGC | 7464 |
rs112635427 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98146029 | CTGGCCTTTAAGATC[A/G]TGGCAGTGAAATGCT | 7464 |
rs112749928 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98189629 | CCCCCATTTCACAGA[C/T]GGAGAAAGTGAGGTC | 7464 |
rs112828348 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | CORO2A | GRCh38.p7 | 9:98130369 | TGGAATTATAGGCAT[A/G]AGCCACTGTGCTGGG | 7464 |
rs112884192 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98124973 | GAAAGCTAAACCACT[A/G]TCCCTCTTTGACTCA | 7464 |
rs112900304 | in-del | -/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98188402 | GATTGTAAGCTCTTT[-/G]GGGGGAAGATCTTTC | 7464 |
rs113088979 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98188094 | CACTCTGTCCCAGCT[C/T]GTGCTTCTCTGAACA | 7464 |
rs113111117 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174388 | TCCTACATGTATATT[A/C]CTGTTTTGTCAAATA | 7464 |
rs113180545 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | CORO2A | GRCh38.p7 | 9:98182404 | GATGAGGCTAGTGAC[A/C]CTGCCAGCAAGCTCT | 7464 |
rs113243731 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98145337 | ACTTCTGGTCCTGGC[G/T]TTGTCCTTTGGGGAC | 7464 |
rs113299878 | snp | C/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98138440 | AAGAAACTGGTTCAC[C/T]AATGTTCACAACAAT | 7464 |
rs113301943 | in-del | -/ACT | 0.395453 | 0.203331 | intron-variant | CORO2A | GRCh38.p7 | 9:98164940 | GGTCACTCTCCCACC[-/ACT]ACTACCACCACCACC | 7464 |
rs113390288 | in-del | -/AC/CACA/CACACC | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98158837 | ATTAAAAAGAAGAAA[-/AC/CACA/CACACC]ACACACACACACACA | 7464 |
rs113426155 | snp | A/C | 0.0693013 | 0.172766 | intron-variant | CORO2A | GRCh38.p7 | 9:98163188 | CATCGCACTGAGTTT[A/C]TTTCTTTTTTTTTCT | 7464 |
rs113453126 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98178007 | AATAGAAACCCCAGT[A/G]TTAATTCTCTCACTT | 7464 |
rs113480891 | snp | G/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98138640 | GGCCAGGCACAAAAG[G/T]CCACACGTTGTGTGA | 7464 |
rs113491541 | snp | A/T | 0.424968 | 0.178567 | intron-variant | CORO2A | GRCh38.p7 | 9:98189894 | ACTCCTTTATTTTTT[A/T]TTTTTTTTGAGATGG | 7464 |
rs113574541 | snp | C/T | 0.132751 | 0.2208 | intron-variant | CORO2A | GRCh38.p7 | 9:98153440 | AGAGATGGGGTCTTA[C/T]TCTGTCACCCAGGCT | 7464 |
rs113628722 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121393 | GCAAGTTCCACTACA[G/T]CAGCTCAAGAACATA | 7464 |
rs113688775 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | CORO2A | GRCh38.p7 | 9:98127400 | GGAGCAGCTGGGGTG[A/G]CTGCTTCTGCTGGGC | 7464 |
rs113704606 | snp | A/T | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98142070 | TAAAAAAGGTGTTTA[A/T]AAACAAAAATACAGA | 7464 |
rs113780358 | snp | A/G | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98132900 | CCAGCAATCCCGAGA[A/G]GACAGACAGGGATGC | 7464 |
rs113934284 | snp | A/C | 0.5 | 0 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123744 | CACTGCAACCTCCGC[A/C]TCCCAGGCTCAAGCG | 7464 |
rs114069454 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CORO2A | GRCh38.p7 | 9:98184914 | ATGAATAGGTAGGTG[C/T]CTGGCATTTTGTAGT | 7464 |
rs114086244 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | CORO2A | GRCh38.p7 | 9:98155296 | TTCCACTCTATAGCT[C/T]GCCTTTCCTTTTGCT | 7464 |
rs114094433 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98141284 | AGGGCGGTACCTGGA[G/T]CTAGGGTCTTAGAAG | 7464 |
rs114101212 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98188847 | ACTAGTACAATGTAG[A/G]TGCTTAATAAATACT | 7464 |
rs114256539 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | CORO2A | GRCh38.p7 | 9:98176165 | TGTGCTGGGAGGCAC[A/C]AAAACCCTCTGAACC | 7464 |
rs114326893 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | CORO2A | GRCh38.p7 | 9:98137361 | TTTATATGGGGGGGA[A/T]CTAAGGCCCATAGAG | 7464 |
rs114445793 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | CORO2A | GRCh38.p7 | 9:98146418 | GCAAGAGGGAGGGAC[A/C]CTGCCTGCAGTGTCA | 7464 |
rs114451200 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CORO2A | GRCh38.p7 | 9:98143930 | AAATGCTTCTTGGCT[A/G]GGCACAGTGGCTCAT | 7464 |
rs114525444 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98175661 | GTTTATTTATTACAC[A/C]ACACAATCGCATGGA | 7464 |
rs114589766 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | CORO2A | GRCh38.p7 | 9:98155317 | TCCTTTTGCTATTTT[A/C]TTTAAGGGAAATTTT | 7464 |
rs114654572 | snp | A/G | 0.0648419 | 0.167978 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174506 | AAAATCTTGGCAGTG[A/G]TGGTGATATGGTTTG | 7464 |
rs114656563 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98189134 | GAACCAAATGAAATT[A/G]CCATTTCTTGTAAGT | 7464 |
rs114874639 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CORO2A | GRCh38.p7 | 9:98168316 | CTATCTGCCACTCTG[C/G]GCAAGTTACTTAATG | 7464 |
rs114966655 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | CORO2A | GRCh38.p7 | 9:98147511 | TTTCCATAATTATGA[A/G]CCTGAGCTAGATTAG | 7464 |
rs115004827 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120835 | TTTCCCTATCCTGGC[C/T]CTCCCCATTCCCGCA | 7464 |
rs115020888 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | CORO2A | GRCh38.p7 | 9:98179381 | TGGACATGGGTCCTG[C/G]GTCTCATGAAGCAAT | 7464 |
rs115062197 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122569 | TTTAGAGTAGGGCTC[A/G]GAACACAGATTCACT | 7464 |
rs115153880 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | CORO2A | GRCh38.p7 | 9:98188788 | AAACAACAACAACAA[A/C]AAAAAACAACAACAA | 7464 |
rs115154865 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174264 | CTGTGCCTCAGTTTC[A/C]TAAGCTGTAAGCTGG | 7464 |
rs115218865 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CORO2A | GRCh38.p7 | 9:98130147 | GCTGGAGAGCAGTAG[G/T]GCAATCACAGCTCAT | 7464 |
rs115220989 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98180213 | TGAGCCAAACCAGAC[C/T]CTACGTTCATCGCAT | 7464 |
rs115259075 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CORO2A | GRCh38.p7 | 9:98158647 | GTAATAACAGAGATT[C/T]GCACATGACAGTCAG | 7464 |
rs115276289 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98167367 | TTGCAAGATAAAGAG[C/T]TCTAGAGATGGATGG | 7464 |
rs115311131 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | CORO2A | GRCh38.p7 | 9:98164807 | GGTCCTTGCCGCTCT[C/G]CACAGAAGTAGGGCA | 7464 |
rs115339511 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CORO2A | GRCh38.p7 | 9:98155125 | GATGTGTAGTGGTAT[C/T]GCACTGGTTTACTAA | 7464 |
rs115432048 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123562 | GTGCAGTCCGCAATC[A/G]TGGCTCATAGCAACC | 7464 |
rs115463366 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98152127 | CGGCCTCTTTTGCTG[G/T]TTTTTTTTTTTGTTT | 7464 |
rs115548179 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CORO2A | GRCh38.p7 | 9:98152782 | TGAGGAAACAATTTG[G/T]TAAGTCCAAATTTAG | 7464 |
rs115552380 | snp | C/T | 0.0178098 | 0.0926698 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120567 | CCCAAATTCCAGTTG[C/T]CCCCCCAGGCTCAAG | 7464 |
rs115559008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98126322 | TACAAGAGTGAGCCA[C/T]TGTGCCCAGCCTCCC | 7464 |
rs115599485 | snp | C/G/T | 0.0221141 | 0.102801 | intron-variant | CORO2A | GRCh38.p7 | 9:98150533 | AATGCCTTCCCAGAC[C/G/T]ATCCTGCCTAAACTA | 7464 |
rs115710913 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122139 | CTGGACTTTTAAGGA[A/G]CCACCAGGCAGGACT | 7464 |
rs115712736 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98159483 | CTAGCTCATCTAAAC[A/G]GCACCTTCCAGCTTC | 7464 |
rs115718364 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98162388 | CTGGAAAGGCTCCCC[A/G]CTTCCCCACGGATGA | 7464 |
rs115840045 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98179457 | TCCTTCCTGCCTCCT[C/T]CAGGCTGTCCTCATC | 7464 |
rs115844451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137267 | CATAGCCTTTTATAG[C/T]TCCCCGAAGGATGGG | 7464 |
rs115910572 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98151056 | ATATACAGTTGCACC[A/T]CCATGCCTTTGCTTG | 7464 |
rs116072035 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98131656 | CCCGATCTCATTCCA[A/G]TCTTCCCCTACCTGT | 7464 |
rs116095773 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CORO2A | GRCh38.p7 | 9:98158822 | GATTATCAAAGAGAA[A/G]TTAAAAAGAAGAAAA | 7464 |
rs116141217 | snp | C/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174590 | GGAGGGGCCTGGTGA[C/G]AGGTGATTGGATCAT | 7464 |
rs116169461 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98128918 | CTTCACCTTCAAAGA[C/T]TTAAATTATTTTAGC | 7464 |
rs116179079 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98179348 | CTGGCCTGGGCCTGG[C/T]GTGTTGGTGGGCAGC | 7464 |
rs116260521 | snp | G/T | 0.021333 | 0.101051 | intron-variant | CORO2A | GRCh38.p7 | 9:98131885 | ACCCTCAGCCCAGAT[G/T]GCCCTCTCCTTCTCC | 7464 |
rs116332234 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CORO2A | GRCh38.p7 | 9:98148902 | AAGCTGAAAAGGTTA[C/T]ATATTGTATGATTCC | 7464 |
rs116360880 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98158981 | CCCATACCCATAATA[C/G]CAGGGGGCCTCCTCT | 7464 |
rs116417269 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CORO2A | GRCh38.p7 | 9:98150740 | AGTTTGTTTGGTGGA[C/T]GTAATCTTTTACAAG | 7464 |
rs116516216 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | CORO2A | GRCh38.p7 | 9:98137011 | GTTCTTGTCTTAAGC[C/T]ATACCACCATATTTT | 7464 |
rs116582722 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CORO2A | GRCh38.p7 | 9:98181916 | TGTGACCTCAGACAA[A/G]TCCTATGGCCTCTCT | 7464 |
rs116643417 | snp | C/T | 0.114387 | 0.210022 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192961 | GGATGAGGAACCTGA[C/T]CTCCCGGAGCCTCAG | 7464 |
rs117001594 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98132475 | GGATCCCTCTCATCC[A/G]CATGGAGTCTCTCCC | 7464 |
rs117068897 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CORO2A | GRCh38.p7 | 9:98156805 | CCACATTGTGGATGC[C/T]TTCCTCTGGAGAGGC | 7464 |
rs117118825 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | CORO2A | GRCh38.p7 | 9:98128456 | ACCCAGGACTCCTGA[C/G]GCCCACTGATGTCAC | 7464 |
rs117195204 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | CORO2A | GRCh38.p7 | 9:98153327 | GCTGATGTCGAACTC[C/G]TGACTTCAAGTGATC | 7464 |
rs117234473 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173845 | CTTTGGTCTGGGTGT[A/G]GTGGCTCACGCCTGT | 7464 |
rs117256347 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98127309 | CCCCCAAGGCAGAGG[C/T]TCTTCCAGTACACCA | 7464 |
rs117260618 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | CORO2A | GRCh38.p7 | 9:98152243 | CAAGTTACATTTTTC[C/T]AGTCTTACTGTGCAG | 7464 |
rs117344675 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CORO2A | GRCh38.p7 | 9:98138318 | TACTCAGGAGGCTGA[A/G]GTAGAACACTTGAAC | 7464 |
rs117406970 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98190554 | CACATCCCCTCTGGC[A/G]ACAGGGGATGCCTAT | 7464 |
rs117617313 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | CORO2A | GRCh38.p7 | 9:98145661 | AGGCATCTGAGCAGC[A/G]GAGTGATGTGGACAC | 7464 |
rs117715733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156463 | CGTAAGTTTTGTGAT[A/G]TATTTCATTTTATCA | 7464 |
rs117807485 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98129617 | TTCCTCCTTTGTGCT[C/G]TTGCACACGTCAAGT | 7464 |
rs117849617 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193642 | GATAACAGAGTACAC[C/T]GTTACTACTTTACAT | 7464 |
rs117910805 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98168206 | CTTCATAATCACAGA[A/T]GAAACCATACAAGCA | 7464 |
rs117976306 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CORO2A | GRCh38.p7 | 9:98130268 | TATTTTTTCATTTTC[A/G]TAGACATGGGGTCTC | 7464 |
rs117999208 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CORO2A | GRCh38.p7 | 9:98164343 | CCCACTATTATCCAT[C/T]ACAGTTTATCTTGAT | 7464 |
rs118013362 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98181720 | GCCTCCCTCCCCACC[C/T]TTGCCTGCTCAGTCC | 7464 |
rs118170290 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CORO2A | GRCh38.p7 | 9:98162814 | GCATGACTTTAATGA[C/T]TCAGTAATTCAGAGA | 7464 |
rs137868323 | snp | A/G | 0.000626463 | 0.0176873 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157526 | AACTGCAATGAAGTG[A/G]GGGTTCACGGCACAG | 7464 |
rs137881539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98134488 | TAAGATGAGATCATA[A/G]TGGATTAGGTGGGCC | 7464 |
rs137916363 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98160929 | ACCCTCTAGGACTCT[C/T]GTCCTTGGCCAAAGG | 7464 |
rs137965398 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98191737 | ATCCCTTAATGCCAC[A/G]CGGACACAGCACCTT | 7464 |
rs137969522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124661 | GAGAGTTTTGTTTTC[C/T]GGTAAAAAATATAGA | 7464 |
rs138008215 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | CORO2A | GRCh38.p7 | 9:98127608 | CTTGAGGTCAAGAGT[G/T]TGAGACCAGCCTGGC | 7464 |
rs138038622 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98156150 | TGGGCTCAGGTAATC[C/T]GACCTCAGCCTCCTA | 7464 |
rs138042072 | in-del | -/CCCCCC | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193500 | CGGCTACTAAGCTAA[-/CCCCCC]CAGCCACTCCACTCC | 7464 |
rs138066490 | in-del | -/TCC | 0.105214 | 0.203807 | intron-variant | CORO2A | GRCh38.p7 | 9:98154151 | TTCTTTCTTATTCTG[-/TCC]TCCTTGTCTGGTTTT | 7464 |
rs138119548 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164986 | TAGGTGTAACAATTC[-/T]TTTTTTTTTTGAGAT | 7464 |
rs138240215 | snp | C/T | 0.021333 | 0.101051 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185540 | ACTCCAAACCATTGC[C/T]GGAGGCTCGTATCTG | 7464 |
rs138242688 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98151208 | TAGCAGAAAAGCACA[A/G]AGGACTCTAATTCAA | 7464 |
rs138373867 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98143629 | GTAAAGCACTGAAGA[C/T]GGTGCCCAGTACTTG | 7464 |
rs138392112 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO2A | GRCh38.p7 | 9:98128481 | TGTCACACTGGCTGT[A/G]AGAAAGGCCGCTCTG | 7464 |
rs138401545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98176944 | TGTCTTCCTGTACCT[A/G]GATACAGTACCAAAC | 7464 |
rs138418417 | in-del | -/CCAACGCTTAAG | 0.284995 | 0.247539 | intron-variant | CORO2A | GRCh38.p7 | 9:98141339 | CAGGTCTCCATGGGA[-/CCAACGCTTAAG]CCACTGACCCTTTTT | 7464 |
rs138480084 | snp | C/T | 9.93328e-05 | 0.00704674 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134899 | GCCCACGAGTTCCTT[C/T]CTGTAGGCCGTGAGG | 7464 |
rs138532218 | in-del | -/TGTTG/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152136 | TGCTGTTTTTTTTTT[-/TGTTG/TTT]TTGTTTTTTCTTTAA | 7464 |
rs138583944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98169521 | ATATTCCACCCCCAA[C/T]TCTGGCCCTGCACTT | 7464 |
rs138588775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190789 | GTCGAGATGACAGGA[C/G]ACCCAGGTAGCACTT | 7464 |
rs138638360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164448 | CCATTGCGAGTGGGA[C/T]ATCTGGCTCTGAAAT | 7464 |
rs138651729 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98160668 | AAGGAGCAAATCAGC[A/G]GGCTCCGCTCCAGGC | 7464 |
rs138679073 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CORO2A | GRCh38.p7 | 9:98168966 | GGGTTCTCCTAGGTG[A/G]AGGCCAGAAGGCCCC | 7464 |
rs138686399 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123717 | CTGGAGTGAAGTGGC[A/G]TGATCTTGGTTCACT | 7464 |
rs138734683 | in-del | -/T | 0.196149 | 0.244131 | intron-variant | CORO2A | GRCh38.p7 | 9:98141350 | TGGGACCACTGACCC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs138858108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180981 | TGTCCCCAGTAACCT[A/G]GGACATCAGCTCACT | 7464 |
rs138915772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144580 | TATGGAGGAGGCAGG[A/T]AGGAATATACTTTGA | 7464 |
rs138942702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98146797 | TTCCTGAGCCTCAGC[A/G]ACCTCATCTGTGCAA | 7464 |
rs139013955 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98151432 | TTCCTAGGTATCCAA[A/T]CTTCTTTTATTCTAT | 7464 |
rs139062718 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98183271 | ACAATGCTACTGTGC[C/T]TGCAGCCACCCAAAA | 7464 |
rs139089417 | snp | A/G | 0.000153988 | 0.00877328 | missense | CORO2A | GRCh38.p7 | 9:98124847 | TGGACCTCTCGCTGG[A/G]TCAACAGCTCCCGGA | 7464 |
rs139105084 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120673 | TGCTTTTTCAAGACT[C/G]GGGGACGTGCAGTTT | 7464 |
rs139117154 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98151955 | CCATGTAGCTGGGAC[C/T]ACAGGCGCACGCCAC | 7464 |
rs139238220 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98144717 | TCAGGTGGAGGGGAG[A/G]AATCTCAAGTCAGAA | 7464 |
rs139255216 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98131823 | CAGCTGTCCCAATGA[A/C]AGCTCCTTCTCCCCA | 7464 |
rs139405896 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193985 | GTTAGCGTGCAAGAG[C/T]TGGGTATCAAGCATA | 7464 |
rs139447175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98172614 | GGGAAGTTCTTTTCC[A/G]CTACTCTCTCACCTG | 7464 |
rs139478538 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98166327 | TTCCTTGGTTATGAT[A/C]CCAGGAACAGGCAAC | 7464 |
rs139520412 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO2A | GRCh38.p7 | 9:98170752 | CTGGCCGAGAATCCT[A/G]ATTCTGACACCAATT | 7464 |
rs139531268 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182682 | TTGCAAATTTACTCA[A/G]CCTCTCTGGGCTCCT | 7464 |
rs139596317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175332 | CAGGCCCCTGGCAGA[A/G]TCGTGGCTCTTCCCA | 7464 |
rs139648214 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98177994 | ATGAAGTGACTGCAA[C/T]AGAAACCCCAGTGTT | 7464 |
rs139665841 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98144960 | GTGGGACCAGGGACC[A/G]CCCAGAGGAGGCTGG | 7464 |
rs139673189 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174548 | CCACCCAAATCTCAT[A/C]TTGAATTGTAATCCC | 7464 |
rs139770354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162163 | GCTAGTGAACAGCAG[C/G]CCTGGGGGCTGCACT | 7464 |
rs139813409 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98155175 | AAATGCTTATTAGCC[A/G]TTTGGATTTTCTTTG | 7464 |
rs139886402 | snp | C/T | 0.000700841 | 0.0187064 | missense | CORO2A | GRCh38.p7 | 9:98157638 | CGGAACTTGGAGCTC[C/T]GGTACTGGGGGTGCC | 7464 |
rs139891923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98135393 | ATCCTCAGGCACTAG[A/G]GAGCCGGCGAGGTCT | 7464 |
rs139922662 | snp | C/G/T | 0.00112026 | 0.0236453 | missense | CORO2A | GRCh38.p7 | 9:98157582 | TGATAGGCACGGAGT[C/G/T]GTAGCAGTTCTCCTT | 7464 |
rs139951248 | in-del | -/AAACAAAACAAAACA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148751 | GCCAGAGCTTGTCTC[-/AAACAAAACAAAACA]AAACAAAACAAAACA | 7464 |
rs140011056 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98138712 | GCACATTAATGCATC[A/C]CCCTGGTACCTGGTA | 7464 |
rs140018642 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98158972 | ATGGCCAAACCCATA[C/T]CCATAATACCAGGGG | 7464 |
rs140030340 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CORO2A | GRCh38.p7 | 9:98141515 | GTGCCACCACACCCA[A/G]CTAGTTTTTGTATTT | 7464 |
rs140057392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162050 | TACAAGCTGCCAGGC[A/G]CCATTCCAAATGCTT | 7464 |
rs140058760 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145435 | CCTTGAGTATGTTCT[C/T]GTCCAGGATGAACAA | 7464 |
rs140094796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125146 | AGATCCTCCATGAAA[C/T]AGAGGAAAGGATGCC | 7464 |
rs140233730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98129131 | GTCTCACTTTGTTGC[C/T]CAGGCTAGGCTCGAA | 7464 |
rs140259931 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98142189 | GAGCCCACAGCTGCA[C/G]TGTCTTATCCTGCAC | 7464 |
rs140319801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98163656 | TAGTCTGAGGACTAG[C/T]TGAGAGACCCCTCTT | 7464 |
rs140388132 | snp | A/C | 1.65373e-05 | 0.00287548 | splice-acceptor-variant | CORO2A | GRCh38.p7 | 9:98133218 | GTTCCAGATCATCAC[A/C]TGCATGGCAGAGAGC | 7464 |
rs140402837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167236 | GCATGATTCCACTTA[C/T]ATGAGTTACTTTGAG | 7464 |
rs140402983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127132 | TTGTAAGGACAGTCC[C/T]ACCCACACTGCACCC | 7464 |
rs140409615 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | CORO2A | GRCh38.p7 | 9:98155814 | TATTAGTTCTTATTA[G/T]ATTTCAAAGCTCTGC | 7464 |
rs140437249 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98145232 | CTGAGGTAATTCATC[C/G]TACTTTCAGACCTTG | 7464 |
rs140442254 | snp | A/G | 0.00494565 | 0.049481 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132259 | TCTTCAGGTTCCCCA[A/G]AAACAGCACTTTGCT | 7464 |
rs140507340 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CORO2A | GRCh38.p7 | 9:98183893 | TTGAACCCGGGAGGC[A/G]GAGTTTGCAGTGAGC | 7464 |
rs140636868 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | CORO2A | GRCh38.p7 | 9:98179934 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 7464 |
rs140641559 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98150418 | GACACACCAAACCCA[C/T]TCCCACTCAGGGGAA | 7464 |
rs140657482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98176184 | ACCCTCTGAACCGAA[C/T]GAAAGCAGAGAAAGC | 7464 |
rs140773298 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98164013 | GCTGGCTACCAGTGC[C/T]CCTTCGTAAATTTGT | 7464 |
rs140849221 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98125404 | GTACCACCGTGGAAA[C/T]GGAAGCTTAGAGACA | 7464 |
rs140890203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130445 | AAGCCCACCCTTTTT[A/C]CTCTAAGACAGAAGC | 7464 |
rs141005424 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98153558 | ACTACAGGTGTGTAC[C/T]ACTGTGCCCAGCTAA | 7464 |
rs141122526 | in-del | -/ACAG | 0.0263992 | 0.111815 | intron-variant | CORO2A | GRCh38.p7 | 9:98168864 | CATGATGATGGGGAA[-/ACAG]ACACACACATGCAGA | 7464 |
rs141142732 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98162674 | TGCACAAGAACTGCA[C/T]TCATCAGGAAGTTCA | 7464 |
rs141197968 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98134258 | AATAGAATTGAGGTC[C/T]CCTGTACTGTGGGTC | 7464 |
rs141214955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186108 | AGGCTCAAGGCCAGG[C/T]TAGAAGCAGCTGTCA | 7464 |
rs141217499 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173425 | CGGCGTCAGTTTTCT[C/G]AGGTTACACGATTAA | 7464 |
rs141324231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180348 | GCTCAGCTTAGAGAA[A/G]TGCTCCCTCTTCCAG | 7464 |
rs141427053 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | CORO2A | GRCh38.p7 | 9:98145871 | GCATGTGCCACCACG[C/G]CCAGCTGATTTTTTA | 7464 |
rs141427070 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CORO2A | GRCh38.p7 | 9:98183789 | ACATAGCGAAACCCC[A/C]TCTCTACTAAAAATG | 7464 |
rs141438467 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98177685 | TGTTGGCCTGGCTGG[G/T]CTCGAACTCCTGACC | 7464 |
rs141453271 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98149838 | GCAATTAACATGTAT[A/C]TTTGAGCTATTTATT | 7464 |
rs141466107 | snp | A/G | 3.29837e-05 | 0.00406088 | missense | CORO2A | GRCh38.p7 | 9:98128609 | CGACTGCCCTTACCC[A/G]CCGGGGCACAATCAT | 7464 |
rs141502362 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154162 | TCTGTCCTCCTTGTC[C/T]GGTTTTGGTATCAAG | 7464 |
rs141540095 | in-del | -/T | 0.0741063 | 0.177655 | intron-variant | CORO2A | GRCh38.p7 | 9:98172016 | AATAAGTGGGTTTCA[-/T]TTCATGTCCAGCTCC | 7464 |
rs141565492 | snp | A/C/T | 3.29485e-05 | 0.00405874 | missense | CORO2A | GRCh38.p7 | 9:98137595 | CTTCAGAACAGGAGG[A/C/T]GATCTCAAAATCATC | 7464 |
rs141578039 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193845 | TGCCCAGAGCTGGAC[A/G]GGCTCCCTGCCTACC | 7464 |
rs141618230 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98156564 | AGTTTCCAAATGAAT[G/T]GGAATTTAAGATTTA | 7464 |
rs141661585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98160726 | ACTGCTGGGGGTGGC[A/G]GGAGTGCACCTGTCT | 7464 |
rs141688919 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO2A | GRCh38.p7 | 9:98154812 | AAATTATGGCATATC[A/G]ATACAAGTGAATGTA | 7464 |
rs141698764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98127637 | GCCAACATGGCAAAA[C/T]CCCCATCTCTACTAA | 7464 |
rs141701363 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123897 | TGACCTCAGAAGATC[C/T]GCCCAGCTTGGCCTC | 7464 |
rs141724222 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122270 | TGCAGATCACCTGTG[A/G]AGCTTATATGACCAT | 7464 |
rs141998948 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98169738 | GAGAAGCAAAAAGAA[A/G]ATAAAAAAGCATCAT | 7464 |
rs142017165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156982 | TTTTGGGGTCAAACC[A/G]GTTGAATATCCACAA | 7464 |
rs142022784 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98144601 | TATACTTTGAGCTCA[C/G]AGGAGAGGCACACAA | 7464 |
rs142059842 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98146897 | ACAACATAATAAAGA[A/G]CCTCTAAGGCCTGTC | 7464 |
rs142060625 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98142558 | CAGGGCCATGCCCCA[A/C]TTTCCGCAGTGCGGT | 7464 |
rs142085956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179674 | AGGTGAGCAGTCGGC[C/T]GGGCGCAGACACTCA | 7464 |
rs142181678 | in-del | -/T | 0.270351 | 0.24917 | intron-variant | CORO2A | GRCh38.p7 | 9:98164600 | TCTGTAAGGGTTTTA[-/T]TCACAACTGGGCTCT | 7464 |
rs142207274 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CORO2A | GRCh38.p7 | 9:98142085 | AAAACAAAAATACAG[A/G]TTTTCTGAAAAAATG | 7464 |
rs142320389 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98165492 | TGCGCCAAGCCGTGT[C/G]AGGAGCAGGGCTCGG | 7464 |
rs142358735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98130550 | GTCATCCAGAAGGTC[C/T]TACCATGGGGAACAT | 7464 |
rs142391990 | snp | A/G | 0.0360663 | 0.129354 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187097 | ATCCTGGCTAACACT[A/G]TGAAACCCCGTCTCT | 7464 |
rs142420124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183820 | TAAAAAATTAGCTGG[C/G]TGTGGTAGTGCATGC | 7464 |
rs142428490 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122807 | AGGCAGGCTGTGTAC[C/G]TGAGGGCCTTGGTGG | 7464 |
rs142446876 | snp | C/G | 5.19009e-05 | 0.00509389 | missense | CORO2A | GRCh38.p7 | 9:98124831 | TTCCAACTGTTTGGC[C/G]TGGACCTCTCGCTGG | 7464 |
rs142470791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125105 | TTCAAGAAGACTGGA[A/G]TGTTTCAGATGTATT | 7464 |
rs142497032 | snp | A/G | 0.000231625 | 0.0107591 | missense | CORO2A | GRCh38.p7 | 9:98134909 | TCCTTCCTGTAGGCC[A/G]TGAGGTTCCTGGTCA | 7464 |
rs142537222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98148898 | AGCCAAGCTGAAAAG[A/G]TTACATATTGTATGA | 7464 |
rs142543977 | in-del | -/TG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163721 | GCGGGGTGTGTGTGT[-/TG]GTGTGTGTATGTGTG | 7464 |
rs142670321 | snp | A/T | 0.00874735 | 0.0655527 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172634 | TCTCTCACCTGCTTG[A/T]TAACATGGAGATAAA | 7464 |
rs142674193 | snp | C/T | 3.35233e-05 | 0.00409396 | missense | CORO2A | GRCh38.p7 | 9:98157644 | TTGGAGCTCCGGTAC[C/T]GGGGGTGCCATGACA | 7464 |
rs142834893 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174257 | AACCTCTCTGTGCCT[C/T]AGTTTCCTAAGCTGT | 7464 |
rs142862966 | snp | C/T | 0.000625792 | 0.0176778 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137659 | TCTGTGCCCGCAGAC[C/T]TTTGGGTAGTGGGGG | 7464 |
rs142866676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177190 | TTCTGCTAGAAAGGC[C/T]GGCAGAGCATCAGCA | 7464 |
rs142876377 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98188873 | ATACTGGCTGAATGA[A/C]TAATGGAATGAATGA | 7464 |
rs142876769 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO2A | GRCh38.p7 | 9:98141057 | GATGGATGTAACTTA[C/T]CCTCAAAGAGTTCTG | 7464 |
rs142916239 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98144269 | CCCAGTGCCAGCTGC[A/G]TTGCTCATAATATTT | 7464 |
rs142917141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98181553 | CCGAAATATGTAAAC[A/G]TGAGCAGACCCCTCG | 7464 |
rs143039943 | in-del | -/CAGACGGTCCC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191249 | TCACTCCGGACCTCT[-/CAGACGGTCCC]CAGGAGGGGCAGGAA | 7464 |
rs143065854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168822 | GGGGCCAAGTGGCTC[A/G]TGAGAGTTCCAACCC | 7464 |
rs143085295 | snp | A/G | 0.00276547 | 0.0370822 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133059 | GACGGTCCCTGCTCG[A/G]GGGTCAATAACCCGA | 7464 |
rs143189652 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98126297 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAAG | 7464 |
rs143214324 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | CORO2A | GRCh38.p7 | 9:98155227 | TTTTGTGGATTTTTC[C/G]GTACATTTTATACAT | 7464 |
rs143255102 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98151339 | CATGAATATAGTAAA[C/T]ATTTCCATCTATTGA | 7464 |
rs143257131 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123480 | TCCTGCTTAGTCTTC[C/T]CCTATTCTCTCTCTC | 7464 |
rs143294637 | snp | A/G | 0.000578345 | 0.0169952 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128183 | ACCTCGATTCATCCC[A/G]CTGAGCCACTCCTGG | 7464 |
rs143375935 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173821 | GCAAGGAGCTTAAGA[C/G]CGTGTAGCCTTTGGT | 7464 |
rs143420950 | snp | A/C/T | 0.000182105 | 0.0095406 | missense | CORO2A | GRCh38.p7 | 9:98157623 | TTGCCAAAGACATGA[A/C/T]GGAACTTGGAGCTCC | 7464 |
rs143453578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162697 | GAAGTTCATGAGCGC[C/T]TGTGTCGTTTTGTGG | 7464 |
rs143485689 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133158 | ATCTTGGTGACAGCT[A/G]ATCGTACTCATGGGG | 7464 |
rs143494231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166739 | TTCATAGCAGCATTA[C/T]TCCCAATAGCTTAAA | 7464 |
rs143499832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163701 | TGCTCCTTTCTTGAC[A/T]TACATGCGGGGTGTG | 7464 |
rs143540754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141867 | GCCCAACAGTCAGGT[A/G]TTACTGTAAGTGCTC | 7464 |
rs143545016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98191124 | CAAGAAAGACCAGGA[A/G]GCTGAGAAGTGATTC | 7464 |
rs143603482 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98159806 | TGGAGCTTCCTCAGA[C/G]AAGGCTCTGCTCCAG | 7464 |
rs143670573 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98182152 | TGAGCCCTCAAAGGC[A/G]GGCCTGTGTCTGTTT | 7464 |
rs143675715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98181293 | CAATCCATCACTAAT[C/T]CCAGCCTCCTGTCCC | 7464 |
rs143707767 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185611 | GGAGGTTGGCAGGAG[A/G]GGGCTCTGTCTGCAG | 7464 |
rs143803728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144047 | TACAAAAATTAGTCC[A/G]GTGTAGGGATGCACA | 7464 |
rs143871905 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161095 | AAGGGGTTATTTGTC[A/G]TGGAGGACAGCGACC | 7464 |
rs143895097 | snp | G/T | 0.00257026 | 0.0357565 | missense | CORO2A | GRCh38.p7 | 9:98124863 | TCAACAGCTCCCGGA[G/T]CCTTCGGATCTCCTC | 7464 |
rs143908533 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98152741 | ATGCAATATTCTTGC[C/T]AAAAATACATAAATG | 7464 |
rs143921523 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98179174 | CCGGTAAAGTCTCGC[C/T]GACATCTGCGGACTG | 7464 |
rs143950603 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140442 | GAGACCACTGTACTT[G/T]TTTTTTTTTTTTTTA | 7464 |
rs143957553 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120770 | TTTCTACCTTACTAT[A/C]TTTTCCTCCAGGAAG | 7464 |
rs144073064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185625 | GGGGGCTCTGTCTGC[A/G]GTGGGCTCAATTCCC | 7464 |
rs144075865 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98129447 | AAGGAACTGAGGACT[C/G]CTTCCTAGAGGCTCT | 7464 |
rs144091289 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174724 | AGCCCTGTGAAGAAG[A/G]TGCCAGCTTCCCCTT | 7464 |
rs144117834 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98134593 | GAAACAGAGCCTGGA[A/G]TGACGCAGCTATAGC | 7464 |
rs144120813 | snp | C/G/T | 0.000115322 | 0.00759261 | missense | CORO2A | GRCh38.p7 | 9:98129820 | TGTGGGTTATAGGAG[C/G/T]GGTACTCAGTCAGGT | 7464 |
rs144133631 | in-del | -/ACGCTTAAGCCA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141331 | CCCTGGCCCAGGTCT[-/ACGCTTAAGCCA]CCATGGGACCACTGA | 7464 |
rs144159841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98138805 | TGTAATCCCAGCACT[C/T]TGGGGGGCCGAGGCG | 7464 |
rs144229783 | snp | C/T | 0.000153988 | 0.00877328 | CORO2A | 9 | allele_origin=T(somatic)/C(germline) | 9:98124818 | ACTGGGGAAGAAAG[C/T] | 7464 |
rs144237592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170920 | ACAGGACCACAAGGG[C/T]GACAGAGCTGTCCAG | 7464 |
rs144331814 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98165249 | CAGGCGTGAGCCACC[A/G]TGCCTGGCTTACACG | 7464 |
rs144439070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128814 | TGGACCTGAACAGAG[A/T]CCAGTCTCCTCCCAG | 7464 |
rs144449940 | snp | A/C/G | 0.00716784 | 0.0595003 | intron-variant | CORO2A | GRCh38.p7 | 9:98183089 | TCTCCAGAGCTTCAC[A/C/G]GAATTTGAAGGCTCA | 7464 |
rs144507519 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98183547 | TGTATTGCATACATA[C/G]TTGGCCCTCTGTATC | 7464 |
rs144568030 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98154680 | AGGCTGTTTTTAATT[C/T]AAGGTTAATTAAATG | 7464 |
rs144579368 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98144852 | GGCTGAGGGCATGGA[G/T]TCTACTCACCCTGCC | 7464 |
rs144651718 | in-del | -/AG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177486 | TTTTTTTTTTGAGAC[-/AG]AGTCTGGCTCTGCTG | 7464 |
rs144735551 | in-del | -/AG | 0.0182019 | 0.0936463 | intron-variant | CORO2A | GRCh38.p7 | 9:98166117 | TGTAACTGTGCACAC[-/AG]AGTATGGAGAAACAT | 7464 |
rs144748778 | snp | A/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187278 | ACAGAGCAAGACTCC[A/T]TCTCAAAAAAAAAAA | 7464 |
rs144754511 | in-del | -/AGAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163768 | GAGAGAGAGAGAGAG[-/AGAA]AGAGAGAAAGAGACA | 7464 |
rs144771711 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CORO2A | GRCh38.p7 | 9:98156308 | GCCTTCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 7464 |
rs144785169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137187 | CCCTCACAGCCTTTT[A/T]TAGCTCGCTTCCTCA | 7464 |
rs144814364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160328 | GCAGGTAAAAAGAGA[G/T]CACCTGAAACGCAGG | 7464 |
rs144845278 | snp | C/T | 0.00156369 | 0.0279178 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126642 | GTGTTCTGCTGCCCA[C/T]CTTGGCATCTTCTCC | 7464 |
rs144873844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98157753 | GTACATAAGAGGGTA[C/T]GAGCAGGACAGTGGT | 7464 |
rs144993361 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98168101 | TCTAGTCCCACAAGG[C/T]TTCTAAATTAAAGTT | 7464 |
rs145038417 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98177208 | CAGAGCATCAGCAGC[A/C]CCCACGATGTGAGGG | 7464 |
rs145057850 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98180360 | GAAGTGCTCCCTCTT[C/T]CAGGAAGTCTTCCTG | 7464 |
rs145097013 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98175334 | GGCCCCTGGCAGAGT[C/T]GTGGCTCTTCCCACC | 7464 |
rs145132131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98146796 | CTTCCTGAGCCTCAG[C/T]GACCTCATCTGTGCA | 7464 |
rs145135792 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98179160 | CTGCTGTTTGAGTGC[C/G]GGTAAAGTCTCGCTG | 7464 |
rs145140031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98142194 | CACAGCTGCACTGTC[C/T]TATCCTGCACCTGTG | 7464 |
rs145145753 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CORO2A | GRCh38.p7 | 9:98150056 | CCTGCCTCAGCCTCC[C/T]GAATAGTTGGGGTTA | 7464 |
rs145201578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98159482 | TCTAGCTCATCTAAA[C/T]GGCACCTTCCAGCTT | 7464 |
rs145268664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145089 | TCCTTCATCACCCCT[C/G]TCCTTATGAGCACCC | 7464 |
rs145296641 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176509 | TACCTGTTCCTGGAG[-/C]CCCCGCCAGCCACAT | 7464 |
rs145312545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160908 | AGCACATGAGACCTG[C/T]CTGTGACCCTCTAGG | 7464 |
rs145430135 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO2A | GRCh38.p7 | 9:98159091 | TTGAGGAAGGATCTC[A/G]CTCTGTCACCCAGGC | 7464 |
rs145456233 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98162118 | CCCCCGTTCAGATGT[A/C]GGTGTTCAGGCCAGT | 7464 |
rs145467027 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122746 | CTACCTCCTGGGGGA[C/T]TCTTCTGTTAACTAG | 7464 |
rs145492242 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CORO2A | GRCh38.p7 | 9:98148455 | AAAAGAAAGAAGGAA[C/T]ACATAATTGAGGCCA | 7464 |
rs145498547 | snp | A/C/G | 0.0154538 | 0.0865337 | intron-variant | CORO2A | GRCh38.p7 | 9:98127548 | CAGGCCCAGTGGCTC[A/C/G]CACCTGTAATCCCAG | 7464 |
rs145556429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139440 | TGAGACCAGCCTGGT[C/T]AATATGGTGAAACCC | 7464 |
rs145602058 | snp | C/G | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98125179 | GCTCTGAAGTCTGGG[C/G]ATTGGTGTTTTCGCC | 7464 |
rs145660123 | in-del | -/TGTATATA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154328 | TCTTATGTGTTTGTG[-/TGTATATA]TATATATATATATAT | 7464 |
rs145697411 | snp | C/T | 0.000120041 | 0.00774635 | missense | CORO2A | GRCh38.p7 | 9:98134841 | TGAAGAGGATGTTGG[C/T]GGCCGTGGGGTGCCA | 7464 |
rs145700474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162334 | CACTTCCACTCTACA[C/G]AGAAGGAAAATGAGG | 7464 |
rs145809242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142623 | CTGCCCTCGGGCTGA[C/T]GGGAGGCAAAGTGCC | 7464 |
rs145822385 | in-del | -/CCA | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98134623 | CAAGGATGCCTGGAG[-/CCA]CCACCAGAAGCTGGG | 7464 |
rs145825494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98188540 | GAGGCCGAGACAAGC[A/G]GATCATTTGAGGTCA | 7464 |
rs145825818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98176833 | GAAATGGAGTCAGCA[C/T]GCCAAAGGCCACCCA | 7464 |
rs145830556 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121998 | AGGAACACGAGCATC[C/T]GGCCTGTGCAGACAT | 7464 |
rs145886944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176422 | GAGCTCACCCCTGCT[A/G]GGGGAAGATGTGCTC | 7464 |
rs145934383 | snp | A/C | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187162 | GTGGTGGGCGCCTGT[A/C]GTCCCAGCTACTGGG | 7464 |
rs145945479 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | CORO2A | GRCh38.p7 | 9:98152106 | ACAGGCATGAGCCAC[C/T]GCACCCGGCCTCTTT | 7464 |
rs145954718 | snp | A/G | 0.00232093 | 0.0339864 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157577 | GCGGGTGATAGGCAC[A/G]GAGTCGTAGCAGTTC | 7464 |
rs145956518 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98154821 | TTGTATGGATATGCC[A/G]TAATTTATTTATGAA | 7464 |
rs146003769 | snp | A/G | 0.000148288 | 0.00860943 | missense | CORO2A | GRCh38.p7 | 9:98133073 | GGGGGTCAATAACCC[A/G]AATCTTGCGGTCTTT | 7464 |
rs146068753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98138103 | CCAGCAATTCCACTC[C/T]TAGGTCTATCTCCAT | 7464 |
rs146071363 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174536 | GGCTCTGTGTCCCCA[A/C]CCAAATCTCATCTTG | 7464 |
rs146082270 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CORO2A | GRCh38.p7 | 9:98141437 | GATCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 7464 |
rs146093594 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO2A | GRCh38.p7 | 9:98144311 | CAACCACCCCAGGAC[A/G]TAGTACAAGAATTCC | 7464 |
rs146109185 | in-del | -/ACAC | 0.281548 | 0.248002 | intron-variant | CORO2A | GRCh38.p7 | 9:98158837 | ATTAAAAAGAAGAAA[-/ACAC]ACACACACACACACA | 7464 |
rs146113119 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193498 | CCACGGCTACTAAGC[C/T]AACAGCCACTCCACT | 7464 |
rs146179885 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO2A | GRCh38.p7 | 9:98155243 | GTACATTTTATACAT[C/T]CAAGAAATGAGTCTT | 7464 |
rs146190971 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98156634 | AGGAAACCTGGTCTA[C/T]GAGATTCTAATCTGC | 7464 |
rs146214625 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124100 | CTCACTGCAACCCCC[A/G]CCTTCCGGTTTCAAG | 7464 |
rs146301505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142026 | CTTTAATATCTTTGT[C/T]TTATTTTTAGCTATG | 7464 |
rs146320064 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO2A | GRCh38.p7 | 9:98170356 | AGCTTCTTCTGAACC[A/C]CTCCTTGAGGTGGTA | 7464 |
rs146349283 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98185130 | ACTAACAACCCAGCT[C/T]AGGCATCAGCTCCTC | 7464 |
rs146493322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132939 | AAGGCGCAGCCCAGA[C/T]GCTGACAGCATCACT | 7464 |
rs146505000 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98138814 | AGCACTTTGGGGGGC[C/T]GAGGCGGGTGGATCA | 7464 |
rs146544632 | snp | C/G | 0.00502235 | 0.0498593 | intron-variant | CORO2A | GRCh38.p7 | 9:98132144 | AATGACACTGGCTCT[C/G]AGCTGAGGGGTGATG | 7464 |
rs146552729 | snp | C/T | 0.00119737 | 0.0244387 | missense | CORO2A | GRCh38.p7 | 9:98126721 | GTCTGATTCAAGAGC[C/T]GGGGTGAGGCTGGGG | 7464 |
rs146612850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180054 | AAACTGCCTCAAAGT[C/T]TGACATTTTACGATC | 7464 |
rs146730315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162961 | CTCATCTTATCCTGC[C/T]CCATTCCATCTGGCT | 7464 |
rs146742010 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98166835 | ATGGAATAATATTCA[A/G]CCTTCAAAAGGAAGA | 7464 |
rs146742160 | snp | A/G | 8.50145e-05 | 0.0065192 | intron-variant | CORO2A | GRCh38.p7 | 9:98126535 | TGAAAGGCCCACCCC[A/G]TCCTCCTTCACACCT | 7464 |
rs146749790 | snp | C/T | 6.62383e-05 | 0.00575454 | missense | CORO2A | GRCh38.p7 | 9:98134930 | TTCCTGGTCAGCAGC[C/T]GCTTGGGGATGCTCC | 7464 |
rs146851991 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98150183 | TGATCTGCCTGCCTC[A/G]GCTTCCCAAAGTGCT | 7464 |
rs146863613 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98153048 | CTCGTTCTTAGAAGA[C/T]ACAGACCGAAGTACA | 7464 |
rs146887170 | in-del | -/G | 0.328382 | 0.237395 | intron-variant | CORO2A | GRCh38.p7 | 9:98191262 | CTCAGACGGTCCCCA[-/G]GAGGGGCAGGAAGCT | 7464 |
rs146929568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169462 | CCTCTCCCAGGCCAT[A/G]CCAAGGCCTCAGCAG | 7464 |
rs146939534 | snp | A/G | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173585 | TGCTCTGAGGCCAGC[A/G]CTCCGGAACTGGGCG | 7464 |
rs146939576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134259 | ATAGAATTGAGGTCT[C/T]CTGTACTGTGGGTCC | 7464 |
rs146949269 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98139608 | TTCCAGCCTGGGCAA[C/T]AGAGTGAGACTCCGT | 7464 |
rs147040514 | in-del | -/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124015 | GGCTGGTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 7464 |
rs147047380 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98155566 | TGGTTAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7464 |
rs147055260 | snp | C/T | 0.000100135 | 0.00707514 | missense | CORO2A | GRCh38.p7 | 9:98134871 | ACTCCACCAGGCCTA[C/T]TCTGCGCGCGTGGCC | 7464 |
rs147095167 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128658 | GCTTTTGGTTGTGAT[C/T]AGCTTGTAGAAGCGG | 7464 |
rs147200130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148326 | CTTGAACCCAGGAGG[C/T]GGAGGCTTCAGTGAG | 7464 |
rs147210305 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98151700 | CGGAATTTTGCTCTG[C/T]CACCCAGGCTGGAGT | 7464 |
rs147305904 | snp | A/G/T | 9.88784e-05 | 0.00703068 | stop-gained, synonymous-codon | CORO2A | GRCh38.p7 | 9:98129867 | GTCGGCGCTCACCTC[A/G/T]TAGTAGCGGATGTTG | 7464 |
rs147316581 | snp | C/T | 0.000249549 | 0.0111675 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134878 | CAGGCCTACTCTGCG[C/T]GCGTGGCCCACGAGT | 7464 |
rs147409361 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98178182 | CTCCTGAGTAGCTGG[A/G]ACCACAGGCATGAGC | 7464 |
rs147419073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98181695 | CAAGGCTGTTTCTCC[C/T]ATGCAGCGTGCCTCC | 7464 |
rs147443437 | in-del | -/CCAC | 0.0528381 | 0.153711 | intron-variant | CORO2A | GRCh38.p7 | 9:98145863 | GACTACAGGCATGTG[-/CCAC]CACGCCCAGCTGATT | 7464 |
rs147525062 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98164924 | GCAAACAGGGATAAG[C/T]TGGTCACTCTCCCAC | 7464 |
rs147556232 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173642 | ATGGTGCTCCACAGC[C/T]GGAACAAAATCCACC | 7464 |
rs147562860 | in-del | -/TA | 0.00835141 | 0.0640778 | intron-variant | CORO2A | GRCh38.p7 | 9:98147905 | CAGTGAGTGAATGGT[-/TA]TATAAACTGTAGTGC | 7464 |
rs147575964 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98142393 | CTCTGAGGGAGCACC[A/T]GTGAGTGCTCTGTGA | 7464 |
rs147598704 | in-del | -/C | 0.0283406 | 0.115616 | intron-variant | CORO2A | GRCh38.p7 | 9:98134395 | GAGTTGAACAGGGTT[-/C]CCCCCAAAACTCATG | 7464 |
rs147619497 | in-del | -/AT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154362 | TATATACACAAATAC[-/AT]ATATATATATATATT | 7464 |
rs147680752 | snp | A/G | 0.0221141 | 0.102801 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122769 | TTAACTAGGGCTGAA[A/G]TCTGCCCACATCATC | 7464 |
rs147704302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189790 | TCCGGTAATGTAAGC[C/T]TCAGTGCCACTATTT | 7464 |
rs147713758 | snp | A/T | 0.0252325 | 0.109451 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194240 | TGGCAGTGAGCCGAG[A/T]TCACATCACTGCACT | 7464 |
rs147716565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125394 | TGTCCCCACCGTACC[A/G]CCGTGGAAACGGAAG | 7464 |
rs147809487 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173410 | CACTCTGCAGAGCAG[C/T]GGCGTCAGTTTTCTG | 7464 |
rs147818949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98175308 | GGACATGCCTGGACG[A/G]TATTTCCCCAGGCCC | 7464 |
rs147928236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158509 | CACTGTGTGTCTAGG[C/T]CCTGTGCCAGGTACC | 7464 |
rs148025999 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98154727 | GTTTGGCTTATTTCA[C/G]TCAACTTTATCTTTC | 7464 |
rs148078226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181465 | ATAGGCGTGAGCCTC[A/G]GTGCCTGGCTCCAAA | 7464 |
rs148088798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147449 | TCTAGAATCTGGGCT[A/G]AGGAAAGTTCATCAT | 7464 |
rs148110066 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187280 | AGAGCAAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 7464 |
rs148208416 | snp | C/T | 0.000312981 | 0.0125057 | missense | CORO2A | GRCh38.p7 | 9:98133087 | CGAATCTTGCGGTCT[C/T]TGCAGGTGGTGGCCA | 7464 |
rs148237089 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185771 | TCCTGTGGCTGGGGC[C/T]GTTATGATGCCATTT | 7464 |
rs148270502 | in-del | -/CGC | 0.0410537 | 0.137264 | intron-variant | CORO2A | GRCh38.p7 | 9:98169211 | CCTTCCCCGCCCCCG[-/CGC]CGCCCATCCTTCTGG | 7464 |
rs148294306 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123527 | TGGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGC | 7464 |
rs148299045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177441 | CAGGAGGTTAGAGCA[A/G]TGGGCTCCAAACTTT | 7464 |
rs148388649 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140113 | AGGACCCAGGCCCTC[A/G]ACCTCCCACATCCAC | 7464 |
rs148389618 | snp | A/T | 8.23689e-05 | 0.00641698 | missense | CORO2A | GRCh38.p7 | 9:98137592 | CATCTTCAGAACAGG[A/T]GGCGATCTCAAAATC | 7464 |
rs148395322 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98156681 | TGAAGTCCTCTGGGG[C/G]TCTAAGTCTGCTATT | 7464 |
rs148404159 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98148868 | AACTGCGAGAGAAAT[A/G]CAGTGAGTAAAAAAA | 7464 |
rs148433581 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187283 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7464 |
rs148437109 | snp | A/G | 3.29745e-05 | 0.00406031 | missense | CORO2A | GRCh38.p7 | 9:98133054 | TGGAGGACGGTCCCT[A/G]CTCGGGGGTCAATAA | 7464 |
rs148470079 | in-del | -/AAACA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180027 | AAACAAAACAAAACA[-/AAACA]GCAAGCAAAAAAAAC | 7464 |
rs148488963 | snp | A/G | 0.000150581 | 0.0086757 | missense | CORO2A | GRCh38.p7 | 9:98157639 | GGAACTTGGAGCTCC[A/G]GTACTGGGGGTGCCA | 7464 |
rs148548200 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98188756 | GCCTGGGAGACAGAG[C/T]GAGACTCTGTCTCAG | 7464 |
rs148606644 | snp | C/T | 0.00256448 | 0.0357164 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124864 | CAACAGCTCCCGGAG[C/T]CTTCGGATCTCCTCC | 7464 |
rs148635591 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98179349 | TGGCCTGGGCCTGGC[A/G]TGTTGGTGGGCAGCT | 7464 |
rs148688980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98174951 | TCGTAAACTTTGCTA[C/T]GTATATATCACCATC | 7464 |
rs148699072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142041 | CTTATTTTTAGCTAT[A/G]TAAGTTTTGCAATTA | 7464 |
rs148730055 | snp | A/G | | | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134890 | GCGCGCGTGGCCCAC[A/G]AGTTCCTTCCTGTAG | 7464 |
rs148752497 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98165369 | CAACATACCGAACCA[C/T]AGAATAGAAATTTCA | 7464 |
rs148857029 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | CORO2A | GRCh38.p7 | 9:98139562 | AACCCAGGAGGTGGA[G/T]GTTGCGGTGAGCTGA | 7464 |
rs148920033 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CORO2A | GRCh38.p7 | 9:98125969 | GAGATCCACCCGCCT[C/T]GGCCTACCAAAGTGC | 7464 |