SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs148949980 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98181193 | AGCGCGACTCCCTCT[C/G]CAAGTCAGGCCATGA | 7464 |
rs148959568 | snp | C/T | 0.000749868 | 0.0193487 | missense | CORO2A | GRCh38.p7 | 9:98134844 | AGAGGATGTTGGCGG[C/T]CGTGGGGTGCCACTC | 7464 |
rs149006022 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO2A | GRCh38.p7 | 9:98153193 | CAACCCCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 7464 |
rs149006038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98176762 | GGATCCCAGATGTCA[C/T]ATCTCAGAACAAAAG | 7464 |
rs149014719 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CORO2A | GRCh38.p7 | 9:98143891 | GATCAGACATGTTCC[C/T]ATGTCTATAAGAAAT | 7464 |
rs149067377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168431 | TTCCACATACCAACT[C/G]AACCCTCATGCAAGT | 7464 |
rs149077443 | snp | C/T | 0.000769501 | 0.0196 | intron-variant | CORO2A | GRCh38.p7 | 9:98133016 | CCTCTGAGCCTGAGC[C/T]AGCCCCTGGCCCAGA | 7464 |
rs149125179 | snp | C/G | 8.27726e-05 | 0.00643268 | missense | CORO2A | GRCh38.p7 | 9:98126815 | GCCTAAGGGACACCA[C/G]GATTGGGTCTGGAAG | 7464 |
rs149126946 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98159649 | AAGCCACTTCCTCCA[C/G]AGAGTCCTCCTTGAT | 7464 |
rs149167597 | snp | A/C | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193500 | ACGGCTACTAAGCTA[A/C]CAGCCACTCCACTCC | 7464 |
rs149182564 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | CORO2A | GRCh38.p7 | 9:98155519 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 7464 |
rs149223999 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173714 | ACGTGCTTAAGATAC[A/G]GGCTTCAGAGTCAGA | 7464 |
rs149256332 | snp | C/T | 7.3185e-05 | 0.00604873 | missense | CORO2A | GRCh38.p7 | 9:98131020 | GCACGCCCGAGGAGC[C/T]GTCCAGGTCCTCCTC | 7464 |
rs149322272 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98154546 | GAGATGCTTTCCAGT[C/T]GTAACCCTCTCCATC | 7464 |
rs149327659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144826 | GAGAGGAGGCTGAGC[A/G]AGAGGGGTGAGGCTG | 7464 |
rs149381266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170255 | CCTTAGATGGTTCTC[A/C]CCTTCTGCTGTGCCC | 7464 |
rs149390994 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98136297 | CAGGACCTGATTGTC[A/C]CTTTGGTGAAATCAC | 7464 |
rs149497328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156241 | GATGGGGTTTCACCA[C/T]GTTGCCCAGGCTGGT | 7464 |
rs149541604 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174611 | ATTGGATCATGGAGG[C/T]GGTTTCCCCCAGGCT | 7464 |
rs149573684 | in-del | -/TA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154364 | ATATACACAAATACA[-/TA]TATATATATATTTTA | 7464 |
rs149688342 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CORO2A | GRCh38.p7 | 9:98183076 | CATTCACCCTGGATC[A/T]CCAGAGCTTCACGGA | 7464 |
rs149692687 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173199 | TAGAGTTTCTGATTC[A/G]GCAGCGTGGGTGAGA | 7464 |
rs149697121 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO2A | GRCh38.p7 | 9:98148374 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 7464 |
rs149729280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139166 | ACTGCTAATGAGTGA[C/G]GGGTGTCTTTTTGGA | 7464 |
rs149756943 | snp | A/C | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193499 | CACGGCTACTAAGCT[A/C]ACAGCCACTCCACTC | 7464 |
rs149782247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98162323 | ATGATCATGATCACT[C/T]CCACTCTACAGAGAA | 7464 |
rs149784208 | snp | A/C/G | 5.19803e-05 | 0.00509783 | missense | CORO2A | GRCh38.p7 | 9:98134832 | AGCCAGCACTGAAGA[A/C/G]GATGTTGGCGGCCGT | 7464 |
rs149791970 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98125441 | CTCTGGGTCTAAGAC[C/T]CTAAATTAGTACTCA | 7464 |
rs149848288 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121941 | GGCTAGTGCATCAGA[A/C]GGGAGTGAGCCCCAG | 7464 |
rs149942171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98167919 | TGGGTGAGGGTACAA[A/G]AGGATTCATTTGAAT | 7464 |
rs149995996 | snp | A/G | 0.021333 | 0.101051 | intron-variant | CORO2A | GRCh38.p7 | 9:98131953 | CCTCCTCTAGCCAAC[A/G]GACTCCCCTGGGTCC | 7464 |
rs150107665 | snp | A/G | 0.000267277 | 0.0115571 | intron-variant | CORO2A | GRCh38.p7 | 9:98128288 | TCCAGACAGTGAGGA[A/G]GGTGGTAGGGTAGGC | 7464 |
rs150159248 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98190609 | GACGACGTCTGAAGG[C/T]TCCTTTCAGCTCAGA | 7464 |
rs150159551 | snp | A/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123683 | TTTTTTGAGACGGAG[A/T]CTCACTCTGTCACCC | 7464 |
rs150212085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98153966 | ACATGATCATATGGT[C/T]TTTCCTCTTTCACTT | 7464 |
rs150273572 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176191 | GAACCGAATGAAAGC[A/G]GAGAAAGCCTTGTGC | 7464 |
rs150366436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98155963 | TCTTCTCTAATGTAT[C/T]CTTATATTCTCTTTC | 7464 |
rs150422041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184579 | AGTGCTCCCGTCCTC[C/T]ATCCCTATCCCTGGC | 7464 |
rs150429764 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98150898 | CTCTCTCTTTAGGAT[A/G]CAGGTCACATGCCTC | 7464 |
rs150508815 | snp | A/T | 0.00716266 | 0.059414 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120827 | GCCTATGCTTTCCCT[A/T]TCCTGGCCCTCCCCA | 7464 |
rs150561499 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98182588 | GCCTTTTCTTTGTGG[A/G]GTTGGATGAGGAAAA | 7464 |
rs150613810 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98147974 | ACACAGAGGCAGGAG[A/T]GGTGGCTCATGCCTG | 7464 |
rs150673990 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | CORO2A | GRCh38.p7 | 9:98169851 | TAGCAGGGCTCTTAG[A/C]ATGCCCCTTCCTGTC | 7464 |
rs150682499 | snp | A/G | 0.000247192 | 0.0111146 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157583 | GATAGGCACGGAGTC[A/G]TAGCAGTTCTCCTTG | 7464 |
rs150732113 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186912 | ACAGCAGCACTCCAG[A/G]CCTGGACTATTTCTA | 7464 |
rs150771347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151908 | TGCAAGCTCTGCCTC[C/T]CGGGTTCACGCCATT | 7464 |
rs150830280 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98165885 | AGGTATTCTGGGGGT[A/G]GGGCTCACCACTCTG | 7464 |
rs150831358 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | CORO2A | GRCh38.p7 | 9:98144714 | AGGTCAGGTGGAGGG[G/T]AGGAATCTCAAGTCA | 7464 |
rs150887619 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98140804 | TGCCTCCCTCTGGAA[A/C]TACTCTGGCTAATCC | 7464 |
rs150894115 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193913 | CATCCTACAGCTCTG[A/C]TTCAGACCTTCTGGA | 7464 |
rs150896020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125137 | TGCTTCCATAGATCC[C/T]CCATGAAATAGAGGA | 7464 |
rs150990194 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173011 | AGAGTCACCTGGAGG[A/G]CTGGAAAAAAACAAA | 7464 |
rs151021966 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98159925 | ATAAAGAAGATGCTC[A/T]CCCAGCCCACACGGC | 7464 |
rs151033060 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | CORO2A | GRCh38.p7 | 9:98155694 | TCCTTTAAAGAACTA[C/T]TCAGGCTTTCTATTT | 7464 |
rs151042087 | in-del | -/TTATC | 0.0263992 | 0.111815 | intron-variant | CORO2A | GRCh38.p7 | 9:98177778 | TGTGCTCACACCCCA[-/TTATC]TTATATTATATACAA | 7464 |
rs151049934 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98162144 | CCAGTAACCGGGTCA[C/T]ACAGCTAGTGAACAG | 7464 |
rs151137156 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | CORO2A | GRCh38.p7 | 9:98179865 | AAAATTAGCCAGGTG[C/T]GGTGGCAGGTGCCTG | 7464 |
rs151200834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142132 | GCCAAAAACTTCTGT[C/T]ATAAAACTGTAGCTC | 7464 |
rs151263262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98131473 | TGGGATTATAGATAT[A/G]CACCACTGCACCCCG | 7464 |
rs180731326 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163273 | CAGCTCACTGCAACC[C/T]CTGCCTCCTGGGTTC | 7464 |
rs180732824 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98145625 | GCAGAACATTATCTG[A/C/T]AGGCAGCAAGGAGTC | 7464 |
rs180739320 | snp | A/C | 0.00438332 | 0.0466095 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123109 | ATGAAGAAACTGAGA[A/C]CAGAGAGGGCAGGAC | 7464 |
rs180798870 | snp | G/T | 1.66977e-05 | 0.00288939 | missense | CORO2A | GRCh38.p7 | 9:98157464 | GGTGTCCTTACCTGG[G/T]GCAGGGGGATGACGA | 7464 |
rs180827272 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173976 | ACAAAATTAGCCGGG[A/C/T]GTGGTGGCGCATGCC | 7464 |
rs180830414 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98135216 | TAGGCCTCCAAATCT[G/T]CCCTTGAGAGATCTT | 7464 |
rs180832580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183794 | GCGAAACCCCATCTC[C/T]ACTAAAAATGTAAAA | 7464 |
rs180880968 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98168191 | CAAAAGCCACATGTG[C/T]TTCATAATCACAGAT | 7464 |
rs180888815 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98140096 | CTGGCAGAACAGGGA[A/C]CAGGACCCAGGCCCT | 7464 |
rs180889108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160577 | AGAAACAACAAGGAC[A/G]AATGACCTCCCTAGG | 7464 |
rs180890830 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98127862 | AATTGCAGAGGTAGG[A/G]GTGGGGAACAGGGAC | 7464 |
rs180902314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187391 | TTGAACCCGGGAGAC[A/G]GTGGCTGCAGTGAGC | 7464 |
rs180936526 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98151405 | ATTTTCCTTCTAAGC[A/G]TTGCTTGTTTATTCC | 7464 |
rs180950045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98178650 | GGACCACATGAGACA[A/G]GAGACTCCTGGACCA | 7464 |
rs181354470 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98156274 | CAAACTCTTGGGCTT[A/T]AGTAATCCTCTGGCC | 7464 |
rs181407186 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98128347 | GGGAGTCCAGGCTCT[C/T]ACCAACCCCTGCTGA | 7464 |
rs181427394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184289 | GGCTGGTCTCAAACT[C/T]CTGGCTTCCCAAAGT | 7464 |
rs181443882 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147026 | TATCCCAGCACTTTG[A/C/G]GGGGCTGAGGCAGGA | 7464 |
rs181489088 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98151613 | TATATATGTAAATAA[C/T]AGCAGTTTTATTTCT | 7464 |
rs181561876 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173358 | CAACCATCTGGGGGC[A/G]CGGAGGATTATCTCC | 7464 |
rs181570826 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163784 | AGAGAGAAAGAGACA[C/G]AGAGAGTTTCCTGCC | 7464 |
rs181597013 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123531 | GATGGAGTCTCGCTC[C/T]GTCACCCAGGCTGCA | 7464 |
rs181608583 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194131 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 7464 |
rs181672949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98188757 | CCTGGGAGACAGAGC[A/G]AGACTCTGTCTCAGA | 7464 |
rs181753902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189737 | CTTTAGTCTCATGGT[C/T]TTTCTTCTGGATTAA | 7464 |
rs181780482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98168679 | CGTTGGCTAGTAAGA[C/T]TGTTGTGGTCCCAAT | 7464 |
rs181816531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164751 | GACCTAACAGTCTCA[C/T]CCCACAGGGTAATTT | 7464 |
rs182000466 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98169203 | GGTTTCCGCCTTCCC[C/T]GCCCCCGCGCCGCCC | 7464 |
rs182019454 | snp | A/G | 0.039522 | 0.134904 | intron-variant | CORO2A | GRCh38.p7 | 9:98151942 | CTGCCTCAGCCTCCC[A/G]TGTAGCTGGGACCAC | 7464 |
rs182025846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129247 | GTTCCCCATCTCCAT[C/T]CCCACAGCTCCTGTG | 7464 |
rs182056700 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98184499 | TCCACACATACTACT[C/T]TTTCTCTTACCGTGA | 7464 |
rs182119936 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98165113 | AGCTAAGAACAAGCA[C/T]GTACCACCGTGCTTG | 7464 |
rs182123971 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98184678 | GGCTGTGATCTGTGA[C/T]GGGGCCATGGCTGCC | 7464 |
rs182128612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148505 | GTAATTCCAGAAGTT[C/T]GGGGTGGGTGGATCA | 7464 |
rs182139940 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98125368 | CACCCCTATAAGGGT[A/G]GCAGTGCTAGTGTCC | 7464 |
rs182253944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181562 | GTAAACGTGAGCAGA[C/T]CCCTCGGCGGCCATT | 7464 |
rs182260036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161994 | CCCCTGGAGCTCACA[C/G]TCACCTCTGTGGCAA | 7464 |
rs182261443 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CORO2A | GRCh38.p7 | 9:98142330 | GAGCTGGGCTTGAGC[C/G]CAGGCCTCTGGTTCC | 7464 |
rs182264823 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121103 | GAATTTCAGAAACAA[C/T]ATTAAAACAATCATT | 7464 |
rs182304623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178448 | CCACGTGTCCATTCT[A/G]TAAGCGCTAGTTAGC | 7464 |
rs182328812 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98139390 | CCCAGCACTTTGGGA[C/G]GCCAAGATGGGTGGA | 7464 |
rs182562716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98158327 | AAAGTATCTGCCTCA[C/T]AGCCTTGTCATAAGG | 7464 |
rs182580780 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98159897 | AGGTTTGGCTGGGCC[C/T]ACGCTGGTCAAGATA | 7464 |
rs182656004 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98169938 | CTCAGACTGAGCAGT[C/G]TCTCCATCCCATGAG | 7464 |
rs182666961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130129 | TCTCACTTTATTGCC[C/T]AGGCTGGAGAGCAGT | 7464 |
rs182731756 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138061 | AGTCTGGCAGTTCCT[C/T]AAAAGGTTAACCGGT | 7464 |
rs182792070 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185531 | CAATCTTAGACTCCA[A/G]ACCATTGCTGGAGGC | 7464 |
rs182821067 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136052 | CTGTGGGCATAGCTT[C/T]GGGGAGGAAAGCCCC | 7464 |
rs182831889 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176455 | CCAGTGGACTTCCTC[A/C/G]CATCTACTGAACAGA | 7464 |
rs182893587 | snp | A/G | 0.000327835 | 0.0127988 | missense | CORO2A | GRCh38.p7 | 9:98124797 | GCTCTGAGCCCATCC[A/G]CAAGTTTTTGATCTC | 7464 |
rs182914682 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190444 | CTTTCATTTATTATA[C/T]GTTATGTGTTTTTTT | 7464 |
rs182931477 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98153396 | GTAAGCCAGCGCATC[C/T]GGCTGATAACTTTTT | 7464 |
rs182946759 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154974 | TGGTTGGTATTTCTG[G/T]GTCACAGGTATATGC | 7464 |
rs182958220 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98131516 | AGAGATGGGGGTCCT[A/G]CTGTGTAGCTCAGGC | 7464 |
rs182963596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179873 | CCAGGTGCGGTGGCA[A/G]GTGCCTGTAATCCCA | 7464 |
rs183031818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170849 | AACAGCCCTGCCCTG[C/T]CCACCTGTTAGGACG | 7464 |
rs183097875 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | CORO2A | GRCh38.p7 | 9:98174938 | AAAATGGTTAAAATC[A/G]TAAACTTTGCTATGT | 7464 |
rs183107735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165239 | GCTGGGATGACAGGC[A/G]TGAGCCACCGTGCCT | 7464 |
rs183116352 | snp | A/G | 4.94271e-05 | 0.00497102 | missense | CORO2A | GRCh38.p7 | 9:98126598 | ACGTCAAAGCCATTT[A/G]TCAGCCAGGTTTTCT | 7464 |
rs183208033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191536 | GCAGGACCAGCAGGA[C/G]AGGCAGTGACTGGGT | 7464 |
rs183343150 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98161101 | TTATTTGTCATGGAG[A/G]ACAGCGACCCATCCT | 7464 |
rs183431101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190936 | GCCGCAGGGCAAGGT[C/T]ATAGGCACTACTTCA | 7464 |
rs183525812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137041 | TAGAAGTGGGTACAA[A/C]ATGAATTGTAAATAA | 7464 |
rs183599074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98140912 | AAGGACATTATTTAA[A/C]AAATCTAAACAAGAA | 7464 |
rs183662102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181023 | CCTAAAATCCCTCAC[A/G]CCACTGACTTTTTTT | 7464 |
rs183749134 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168057 | GGGGTCTAATCTTGG[A/C]TCTAAACGGCCCTGT | 7464 |
rs183754617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98157854 | GTAGACCTGGTAAGA[C/T]AAGATGGGATGAAGC | 7464 |
rs183757276 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186743 | GGGGATTGGGTTAAC[A/C/G]TATATAAAATATTAG | 7464 |
rs183768611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150678 | CAGTTCTGAGAGTTT[A/G]AGTAATAAAAGGAAA | 7464 |
rs183804340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176974 | CATTTTTGTTCCTTA[C/T]CTGTGTTGCTCTAAG | 7464 |
rs183816263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98138652 | AAGGCCACACGTTGT[A/G]TGATTCCACTTAGAT | 7464 |
rs183819238 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159430 | GGCATTCAAGGCCTC[C/T]GGCTGGGTCTCATTC | 7464 |
rs183898845 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98184011 | TAGCATTTACATTGT[C/G]TTAGGCATTGTAAGT | 7464 |
rs184053136 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98141410 | AGGCTGGGGTGCAGC[A/G]GTGCGATCCCGGATC | 7464 |
rs184291646 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172613 | TGGGAAGTTCTTTTC[C/T]GCTACTCTCTCACCT | 7464 |
rs184298408 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193595 | ACTGCTCCGTGGCAC[A/G]TAGTAACCACTCAAT | 7464 |
rs184309708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156549 | TAGAAATAGTTTTTA[A/G]GTTTCCAAATGAATG | 7464 |
rs184313702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134549 | CTATAAGGAAGACAG[A/G]TACACAGAGAGAAGG | 7464 |
rs184343000 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98127326 | CTTCCAGTACACCAG[A/G]AGGCCCGCTCAGCCA | 7464 |
rs184409839 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133373 | GGAGGATGATGTGCA[A/C/G]GCTGAAGCTGCTTGT | 7464 |
rs184495670 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98171841 | GGGGCGCAGTGCTGA[A/G]GAGGGGGCACCTGAG | 7464 |
rs184555988 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98151590 | CTTTTGGGTTCTATG[C/T]AGACAATTATATATG | 7464 |
rs184585170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150247 | ACAAGTGAGTTTCAA[C/T]CCTCCAGTGGCTTCC | 7464 |
rs184591627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166112 | TTGTATGTAACTGTG[C/T]ACACAGAGTATGGAG | 7464 |
rs184595843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127092 | CCCCAAACACTTCAA[A/T]CTCACATGAGACCTT | 7464 |
rs184614527 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193341 | AGCGCCTTCTGTGCA[C/T]TACCTCGCTTCACTG | 7464 |
rs184622322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155316 | TTCCTTTTGCTATTT[C/T]CTTTAAGGGAAATTT | 7464 |
rs184627475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187761 | TAAGATTTCAACATA[C/T]GAGCTTTGGAGGAAC | 7464 |
rs184692886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127939 | TGTAAAGAAGCTTTC[C/T]GTGGGGCAAAGTCCC | 7464 |
rs184727713 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98145268 | TTGGAGAAAATGTTT[A/C]CTACTTCGAGCCCAG | 7464 |
rs184735247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98171448 | CCATGCTGGGCACTG[C/T]AGGGGAGATGCATGG | 7464 |
rs184740384 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122816 | GTGTACCTGAGGGCC[A/T]TGGTGGTGGCAGTCA | 7464 |
rs184752472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155204 | TGCTATGAAGTGCTG[C/G]TTCAGTGTTTTGTGG | 7464 |
rs184794012 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168207 | TTCATAATCACAGAT[G/T]AAACCATACAAGCAA | 7464 |
rs185074582 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122384 | TTCTAATGTACACAG[C/G]TTGGGTTGAAACCTA | 7464 |
rs185147146 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162305 | TCCCTAAGAGGAACT[C/G]TCATGATCATGATCA | 7464 |
rs185251710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182098 | CTCCTCCAGATTCTG[C/T]GGGACTCTACGATTA | 7464 |
rs185273569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98143122 | CACGCCTGCTCCCCT[C/T]GCAGACCCCACAGAA | 7464 |
rs185280880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98139723 | ATTGCTTGAGCCTGG[A/G]AGGTCGAGGCTGCAG | 7464 |
rs185299735 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98177898 | AAGTGTCCCCTAACA[G/T]AAACAAACAAACAAA | 7464 |
rs185316019 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139012 | AGATCATGCCACTGC[A/G]CTACAGCCTGGCGAC | 7464 |
rs185415416 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159711 | GTTCCCTGACAGCCA[A/C]CTCTCCCCTTGCCTT | 7464 |
rs185429291 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98163334 | AGCTGGGATAACAGG[C/G]GCATGCCACTGTGCC | 7464 |
rs185436471 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185657 | AGCCTGGGCCAACAC[C/T]GTGGTGCAGCCTTAG | 7464 |
rs185446084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183454 | AAAGTCCTTATGCTG[G/T]GAGTGCTGACTTCAT | 7464 |
rs185450356 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123424 | AAAATAGAAGGGAGC[C/T]GTCTGGTTGGAATAC | 7464 |
rs185499399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163008 | CACAACAGGCATTCT[C/G]AGGTGTGGCACTCTG | 7464 |
rs185519434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131826 | CTGTCCCAATGAAAG[C/T]TCCTTCTCCCCATAC | 7464 |
rs185578655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178971 | ATCCTGGAGAGAATG[C/T]AAATCTCTAGGCCTT | 7464 |
rs185586846 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98160767 | GTGATGCTCACCAGA[C/T]GTCCCATTGCTCCCC | 7464 |
rs185588963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98140148 | TAGTTCCAGGTTCTT[A/G]AGCCACCCACCAGAA | 7464 |
rs185717540 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174553 | CAAATCTCATCTTGA[A/C]TTGTAATCCCCAAGT | 7464 |
rs185735572 | snp | A/G | 0.00236953 | 0.0343387 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157649 | GCTCCGGTACTGGGG[A/G]TGCCATGACATCTGC | 7464 |
rs185916332 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98160213 | ACTAATTAATGCCCA[C/T]GTGATTCCAGAAAGG | 7464 |
rs185967271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168736 | AACACACAACAGGTA[C/T]ATGCTGGGAGGCCAG | 7464 |
rs185975517 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189571 | GTTCACTCTAAGAGG[C/T]TGGCTGTCAGAGCTC | 7464 |
rs185977538 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CORO2A | GRCh38.p7 | 9:98151870 | CGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTC | 7464 |
rs185991691 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98128909 | AATCAGACTCTTCAC[C/T]TTCAAAGATTTAAAT | 7464 |
rs186068155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98135398 | CAGGCACTAGGGAGC[C/T]GGCGAGGTCTCTGCA | 7464 |
rs186127589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147742 | ATAAGGCTAAACATG[C/T]AACTACCTTATGACT | 7464 |
rs186127955 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194232 | GGTGGAGGTGGCAGT[A/G]AGCCGAGATCACATC | 7464 |
rs186144649 | snp | C/G/T | 4.06298e-05 | 0.00450702 | missense | CORO2A | GRCh38.p7 | 9:98124859 | TGGGTCAACAGCTCC[C/G/T]GGAGCCTTCGGATCT | 7464 |
rs186144798 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173390 | CTTCGTGAGTGTGGC[C/T]GGGGCACTCTGCAGA | 7464 |
rs186187470 | snp | A/C/G | 0.000757787 | 0.0194509 | missense, synonymous-codon | CORO2A | GRCh38.p7 | 9:98157553 | ACAGAAGTGGTTGTC[A/C/G]TGAACGCTGCGGGTG | 7464 |
rs186269073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190258 | TTAGGATAAAGTCCC[C/T]AAAGTAGCCGGCTAA | 7464 |
rs186282036 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98169281 | ACAGATTGAGTCAGA[C/G]AGCAAACCAAGACAA | 7464 |
rs186383092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163858 | CAGGACAAGGGTTAG[A/C]TGCAGGGTGGCTGAA | 7464 |
rs186588809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184381 | AAAGAAAACAAAATT[A/C]TACCACCTAGTGATA | 7464 |
rs186709866 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123790 | CCTCCCAAATAGCTG[A/G]GATTACAGGCATGCA | 7464 |
rs186808932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165161 | GACAGGGTTTCACTC[C/T]GTTGCCAGGCTGGTC | 7464 |
rs186810809 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98138084 | TAACCGGTTCCCACA[A/C/T]GACCCAGCAATTCCA | 7464 |
rs186815218 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98185238 | CTTCCCTATGATAAC[C/T]GTAGTGCCCCTGCCA | 7464 |
rs186827726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98148586 | CTCTACATAAAAAAT[A/G]TACAAAAATTAGCTG | 7464 |
rs186871823 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141111 | CTACACATTCAGAGG[C/G]AGAAAGAGAACCAAA | 7464 |
rs186918999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147189 | CAAACAAACCACAAG[C/T]AAAGTGGCATGTATG | 7464 |
rs186942855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162172 | CAGCAGGCCTGGGGG[C/T]TGCACTCAGCTGTCT | 7464 |
rs186944676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181739 | CCTGCTCAGTCCCTA[C/T]TCATCTTTCAGATCT | 7464 |
rs186960404 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98142438 | CTCCTTCCTGCACAC[A/T]GCCTTTCCTTTCTCT | 7464 |
rs186978990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180567 | CTTAAAAGAACCATC[C/T]CATCTCCAAATACCC | 7464 |
rs187085373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98156844 | AGTTTCTGCTGTGAG[C/T]CAGTGGCACTACTAA | 7464 |
rs187161192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161107 | GTCATGGAGGACAGC[A/G]ACCCATCCTGATTCA | 7464 |
rs187199932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98136094 | GTCCCCCAACAGTCA[C/T]GTCCTGCCCTGGGGC | 7464 |
rs187228468 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98129680 | TGTCTCTCCTCCCAT[C/T]TGACTCATCCCTGTC | 7464 |
rs187268337 | snp | A/G | 0.000508328 | 0.0159344 | intron-variant | CORO2A | GRCh38.p7 | 9:98134993 | AGGCAGCATTAGCCA[A/G]GGCACCTTGGCACCG | 7464 |
rs187432978 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178545 | AAACCAGGTTAATTA[A/G]TTGGGATAACTTGCC | 7464 |
rs187436328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152566 | TGGGCCCATAGGTGT[A/G]AGCCACCCTGCCTGG | 7464 |
rs187659433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98171085 | CTGGGAGTTTCGAGC[A/G]ACAAGGATCACTGGG | 7464 |
rs187672881 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98155032 | TGCCAGTTTACACTC[C/T]CATCAGAAGTGTCTG | 7464 |
rs187675889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131539 | GCTCAGGCTGGTCTC[A/G]AATTCGTGGCCTCAA | 7464 |
rs187730449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176599 | TGGGATGGCTCCACT[G/T]GGGGGTGGGGGTTTC | 7464 |
rs187777415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98161486 | TTGAACCGGGAATGC[A/G]GAGGTTGCAGCGAGC | 7464 |
rs187787303 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98141609 | TCTGCCCGCCTTGGC[C/T]TTCCAAAGTGCTGGG | 7464 |
rs187792177 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120692 | GACGTGCAGTTTACC[A/C]TGCTTGGAACATTCT | 7464 |
rs187813354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166593 | AGGGTTTAGTTGCTA[A/T]GAAAGATAGTACGGC | 7464 |
rs187819906 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186509 | GACTGAAAGTAAATG[C/T]TCATATTGATTATGT | 7464 |
rs187821994 | snp | A/C/G | 0.0387552 | 0.1337 | intron-variant | CORO2A | GRCh38.p7 | 9:98150431 | CATTCCCACTCAGGG[A/C/G]AATGTTTGCATGTTC | 7464 |
rs187833201 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121621 | CCAAGGAATGGCATT[A/G]TGCAGAGGCATACCG | 7464 |
rs187836010 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98127137 | AGGACAGTCCCACCC[A/G]CACTGCACCCCACCA | 7464 |
rs187837139 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98153518 | CTCAAGCAATTCTCC[G/T]GCTTCAGCCTCTCGT | 7464 |
rs187928366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190597 | GGGGTTGAATGAGAC[A/G]ACGTCTGAAGGCTCC | 7464 |
rs187971775 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98126246 | TCACTATGTTGGCCA[C/G/T]GCTGGTCTTGAACTC | 7464 |
rs187974844 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98191959 | CCAGGCAGTCGTGCC[A/G]CCAGGAGTCCAGCCA | 7464 |
rs187989494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165321 | AAGTTGTCTGCGAGA[C/G]AGGAGGCTCTAGAAT | 7464 |
rs188028458 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98158726 | AGTAGGAGTTGGTCA[C/T]GTAGGCAGGATGAGG | 7464 |
rs188103233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178572 | TGCCAAAAACAGACT[A/G]AAGAGTAAGGGAGTC | 7464 |
rs188119152 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187083 | AGGAGATTGAGGCCA[G/T]CCTGGCTAACACTGT | 7464 |
rs188121525 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170349 | CACCAGCAGCTTCTT[C/T]TGAACCCCTCCTTGA | 7464 |
rs188125117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160475 | ATTTGGTGTCTATAA[C/G]ATAAAAGCCACAAGT | 7464 |
rs188129455 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168064 | AATCTTGGCTCTAAA[C/T]GGCCCTGTCCAACAC | 7464 |
rs188133372 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98139727 | CTTGAGCCTGGGAGG[C/T]CGAGGCTGCAGTCAG | 7464 |
rs188218739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182109 | TCTGTGGGACTCTAC[C/G]ATTACTGTCCATCTC | 7464 |
rs188282259 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98149510 | GGCAAAAGAAGCCTG[G/T]CACCAGCATCTGCTT | 7464 |
rs188471875 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98133900 | CTGGGACTACTTGAC[A/G]CATTTTCCCACACCT | 7464 |
rs188628247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177065 | TTATAATTGTGAGCT[C/G]AAGGGTCATTGGCCT | 7464 |
rs188637813 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159593 | CCCCCACCTCCTGTT[A/C]CCATCTCCACAAATC | 7464 |
rs188639670 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98138707 | CCTGAGCACATTAAT[A/G]CATCCCCCTGGTACC | 7464 |
rs188669832 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98163778 | AGAGAGAGAGAGAAA[A/G]AGACAGAGAGAGTTT | 7464 |
rs188672269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98184278 | TTTGTTGCCCAGGCT[A/G]GTCTCAAACTCCTGG | 7464 |
rs188718254 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158176 | CTCAGCTAGGCATGG[C/G/T]AGCTCATGCCTGTAA | 7464 |
rs188757331 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193976 | GCTTCTGGTGTTAGC[A/G]TGCAAGAGTTGGGTA | 7464 |
rs188769847 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172910 | AAAGGCACTTCTGCC[C/T]GCAAGACTGGCTGTG | 7464 |
rs188782809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98132077 | GCACCTGGCAGTCTA[C/T]GCTAAATGTGTGTGT | 7464 |
rs188790843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98156590 | ATTTATCTTTTGTTA[C/T]TGATTTCTAACTCAA | 7464 |
rs188872745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171701 | ATGGGGTGGAAGGCG[C/T]TGTGCTAGGTCATGC | 7464 |
rs188916499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137272 | CCTTTTATAGCTCCC[C/T]GAAGGATGGGTTTTC | 7464 |
rs188999992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98175955 | TTATTGAGTACTCAC[G/T]GTGAGCCAGGCACTG | 7464 |
rs189057904 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98181332 | ATCATCTCTCTCTCT[A/T]GCTTTTTTTTTTTTT | 7464 |
rs189063835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155254 | ACATTCAAGAAATGA[A/G]TCTTTTGTCATGTTT | 7464 |
rs189089571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98134566 | ACACAGAGAGAAGGC[C/T]GTGTGAAGACAGAAA | 7464 |
rs189332255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98151074 | ATGCCTTTGCTTGTG[C/T]CCTTCCCTTTGCCAT | 7464 |
rs189477416 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193434 | AGAGATATTAAGTAC[C/T]TAGGTTAAGATCACC | 7464 |
rs189485738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156177 | CCTAAGTAGCTAGGA[A/C]CACAGGCAAATGCCC | 7464 |
rs189536226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183538 | ATTATAACTTGTATT[A/G]CATACATAGTTGGCC | 7464 |
rs189546131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145413 | ATTTGAAGACAGAGG[A/G]CCCATTCCTTGAGTA | 7464 |
rs189547795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163046 | CTGCTGGGCACAAGG[C/T]GGGAGGTGGCATCCA | 7464 |
rs189562304 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123037 | TTTCTCTTAGGTCAA[C/G]GTTTCAGGTGGCAGA | 7464 |
rs189613966 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CORO2A | GRCh38.p7 | 9:98127471 | AGGCAGAGTGGGCAG[A/G]GGGACCTGGGTGGGG | 7464 |
rs189652591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168553 | TGGAATCTGAAGCCA[A/G]GCTGTTCAGTCACAG | 7464 |
rs189746768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98146497 | GAAGGACTTCCTGCA[C/T]GCTGTGGCAAGGCCA | 7464 |
rs189754440 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98185265 | GCCAGGCCATGGGCC[C/T]TCACGGCTGTGATGG | 7464 |
rs189767167 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172045 | CCAGTGGGCTGGAGG[A/G]GTTGCGGAACCCCAT | 7464 |
rs189903171 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98188582 | CCAGCCTGGCCAACA[A/T]GGCGAAACACCGTCT | 7464 |
rs189912284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151600 | CTATGTAGACAATTA[A/T]ATATGTAAATAATAG | 7464 |
rs190237029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135891 | GTCACTGCATAGAAC[C/G]CCGGGAGGAAGACAC | 7464 |
rs190289182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98159825 | GCTCTGCTCCAGGAG[C/T]GTCCAGCACAGTGTC | 7464 |
rs190304576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140857 | GTGATCAGACACCTC[C/T]GCCTAGACTGGATCC | 7464 |
rs190371726 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CORO2A | GRCh38.p7 | 9:98153663 | AAACACACACACACA[C/T]ACACACACACACACA | 7464 |
rs190381403 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98131488 | GCACCACTGCACCCC[A/G/T]CTGATTTTTTGCAGA | 7464 |
rs190385606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161098 | GGGTTATTTGTCATG[C/G]AGGACAGCGACCCAT | 7464 |
rs190389395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98162725 | TGGGTGTGCATGCAC[A/G]TGTGCATCCCTTTGG | 7464 |
rs190393967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179751 | GGCTCTTGCCTGTAA[A/T]CCCAGCACTTTGGGA | 7464 |
rs190407678 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122549 | TATTGTATTGACCAC[C/T]GAACTTTAGAGTAGG | 7464 |
rs190444297 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173561 | TCTCTTCTCAACATA[C/T]AAATTGCATGCTCTG | 7464 |
rs190450906 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136801 | ACAGTGGGCTCACAA[C/T]AAATGGTGACAATGA | 7464 |
rs190450907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98157773 | AGGACAGTGGTCAGT[A/T]CAACGTGGACGGTGA | 7464 |
rs190534931 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174798 | TGTGGAACTGTGAGT[C/T]AATTAAACCTCTTTC | 7464 |
rs190544988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178409 | GCTAACAAGTCACAA[A/T]TTTTCAGTACGAATC | 7464 |
rs190549721 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139321 | ACAGGACAAAACCCC[A/G]TCTCTACAAAAAATC | 7464 |
rs190605007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153092 | AAGGGTCATCTCTAT[A/G]ACTTTTTCTCTTTTT | 7464 |
rs190675896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98190377 | TTGCCAGCACAGAGT[C/T]TCATCTTTTTATTTT | 7464 |
rs190775861 | snp | A/C | 0.00557542 | 0.0525036 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194406 | GCACCATGATCTTTC[A/C]CAGGCTAAGGCATCT | 7464 |
rs190799197 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98129036 | CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTTAG | 7464 |
rs190846649 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169363 | ATCTGACACTGCCCA[C/G]AGCCACCGTCCCTGG | 7464 |
rs190857138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98130037 | CCAGGAAACTGGGGG[C/T]CCTGTCATCAAGGCA | 7464 |
rs190872023 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98168977 | GGTGGAGGCCAGAAG[G/T]CCCCACCCTGCCCTA | 7464 |
rs190877423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98189596 | GAGCTCAAACAAATT[C/T]AGCAACTGCTGAGTC | 7464 |
rs190879463 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98151909 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 7464 |
rs190937778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98125001 | TCAGAAAGGTGGAGG[C/T]GGTCACATTAACATG | 7464 |
rs191016127 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98165107 | CTGCATAGCTAAGAA[A/C]AAGCATGTACCACCG | 7464 |
rs191026295 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98148247 | TGAAAATATAAAAAC[C/T]AGCCAGGTGTGGTGG | 7464 |
rs191096624 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120749 | TATTCCAACTTACTC[A/T]GCAGGTTTCTACCTT | 7464 |
rs191132307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165182 | CAGGCTGGTCTTGAA[C/T]ACCTGGCCTCAGGCG | 7464 |
rs191166666 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181366 | TTTTTTTAAGAGATG[A/G]GGTCTCACTATGTTG | 7464 |
rs191176882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141791 | TCTGTAAAATGTGAA[G/T]GAATAATCATTTCTT | 7464 |
rs191177044 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98161795 | TGGCGGGCCTGGGGT[A/C]GTCGCTGAAATCGAC | 7464 |
rs191303956 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98176782 | CAGAACAAAAGCACT[A/G]GCCAGACCCCAAGAG | 7464 |
rs191317515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98170624 | TTTTTGTATTTTTAG[C/T]AGAGCAAAGGGGCTT | 7464 |
rs191328855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158908 | ACAAGCCAGAGGGGC[A/G]AGGAGAGCCAGATCA | 7464 |
rs191383271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184403 | CTAGTGATAATTAGC[C/T]TGATGTCTGTCTGAA | 7464 |
rs191391187 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174196 | AAAGTTCTCAATAAA[C/T]GGTAGCAACCAGTGG | 7464 |
rs191394215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148704 | CTGCAGTGAGATATG[A/G]TCATGCCACTGCATT | 7464 |
rs191411865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147453 | GAATCTGGGCTGAGG[A/G]AAGTTCATCATATTA | 7464 |
rs191542397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98190925 | GCTCCACCATGGCCG[A/C]AGGGCAAGGTCATAG | 7464 |
rs191634356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138647 | CACAAAAGGCCACAC[A/G]TTGTGTGATTCCACT | 7464 |
rs191655164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98163863 | CAAGGGTTAGCTGCA[A/G]GGTGGCTGAAACTGA | 7464 |
rs191664368 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124148 | CCTCCCAAGTCGCTG[A/G]AATTACAGGCGCCTG | 7464 |
rs191794426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98182002 | CCTTGACCGGCACCA[C/T]CTGTGCCCTGGACTG | 7464 |
rs191864378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172577 | CCCACTTCTGAGCTC[A/G]ACCCCACAGCGGGAA | 7464 |
rs191936291 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98161141 | AGCCTATGCAAGTCC[A/G]GCCCATGGAGATGGC | 7464 |
rs191937195 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98159686 | AGTAGCAGAGATCTC[A/G]CTCTCCTCTGTTCCC | 7464 |
rs191942200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177192 | CTGCTAGAAAGGCCG[A/G]CAGAGCATCAGCAGC | 7464 |
rs192181930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191335 | CAAGCCCCAGGAAAG[C/T]GGAGGCCCCACAGCC | 7464 |
rs192184912 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193108 | GCTCCTTTCCCCGAG[C/T]AGTTACAGCGGTTAC | 7464 |
rs192193142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171189 | CAGAGCTTTCAGACC[C/T]GTCTTTGGACAGAGA | 7464 |
rs192197274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98155287 | TATATCCTTTTCCAC[C/T]CTATAGCTCGCCTTT | 7464 |
rs192242150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180649 | TCATTAGGTGAAAAT[A/G]CTCCACCTGCTTCCA | 7464 |
rs192268480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98141141 | AAAAAAAGGAAAGAA[C/T]GTGGACTTGTGTCCT | 7464 |
rs192351261 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98157103 | GTTTTGACTCAATGT[G/T]TGTTTCCCTTTTTTT | 7464 |
rs192488557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155155 | ATGAGGTTGAGTAGT[G/T]TTTCAAATGCTTATT | 7464 |
rs192493972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131554 | GAATTCGTGGCCTCA[A/G]GTGATCCTCCCGCCA | 7464 |
rs192595655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150472 | GCCAGCATACTCTCC[C/T]TTTAGAGCCTCAAGT | 7464 |
rs192602597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171830 | GAGAGGTGCTGGGGG[C/T]GCAGTGCTGAGGAGG | 7464 |
rs192607885 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127273 | GTTATCCAAAACTAG[A/G]ACTCGGCCCTGGTCC | 7464 |
rs192613431 | snp | A/G | 0.000331329 | 0.0128668 | intron-variant | CORO2A | GRCh38.p7 | 9:98132322 | GGGACACGTGCGGTC[A/G]GTATTGGAGAGACAG | 7464 |
rs192691818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126430 | GTCAAGTGACTAGGC[C/G]AGGCCACACAGCTGG | 7464 |
rs192695677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167898 | GCTGCTGATGGCTAC[A/T]GAAAGTGGGTGAGGG | 7464 |
rs192698214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186684 | ATATCCATTTTAAAA[C/T]GGGAGAAATAATAAC | 7464 |
rs192766922 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142876 | CCTGCGCTGCCCTGC[C/G]CTGCCCTGCCCTGGG | 7464 |
rs192836416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185644 | GGCTCAATTCCCCAG[C/G]CTGGGCCAACACCGT | 7464 |
rs192844150 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149835 | ATAGCAATTAACATG[C/T]ATCTTTGAGCTATTT | 7464 |
rs192921582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98162885 | AGTGAGTACTGTAGC[A/G]GGCCCTTCGCCTACA | 7464 |
rs192924976 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122558 | GACCACTGAACTTTA[C/G]AGTAGGGCTCGGAAC | 7464 |
rs192964237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162277 | CCCATCACAGCCCTG[A/G]ATCTCACCTCTGTCC | 7464 |
rs192977310 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121969 | CAGTGACTGAGTAAA[C/T]GGAGAATAAGACAAG | 7464 |
rs193004933 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193505 | TACTAAGCTAACAGC[A/C]ACTCCACTCCACACC | 7464 |
rs193046466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98138919 | CGGCGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 7464 |
rs193051754 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98165429 | GAGAGGTGAAGAGGA[G/T]TTCATTCAATCTCCA | 7464 |
rs193130710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176400 | CTCGTACCAGTCTAG[C/T]GATGGGGAGCTCACC | 7464 |
rs193131578 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98137796 | AAAACATAAGGGACA[C/G]AGCTGGGTGTGAATC | 7464 |
rs193157708 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182343 | TACAGTCTTTCTCCA[C/G]GGCAGGCCACACAGG | 7464 |
rs193165322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98144512 | CCAGACTGCATGCAG[C/G]TGATGGCAGAGATGC | 7464 |
rs193282305 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158179 | AGCTAGGCATGGCAG[C/T]TCATGCCTGTAATCC | 7464 |
rs199540896 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163747 | GTGTGTGTGTGAGAG[A/T]GAGAGAGAGAGAGAG | 7464 |
rs199562357 | snp | C/T | 0.000231481 | 0.0107558 | intron-variant | CORO2A | GRCh38.p7 | 9:98137528 | CCCAACCACCCCAAT[C/T]CCACTCTTCAGGAAG | 7464 |
rs199663230 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144207 | AAAAAAAAAAAAAAA[-/A]GCTTTTCTTTAGAAA | 7464 |
rs199681026 | snp | C/T | 9.88761e-05 | 0.00703052 | intron-variant | CORO2A | GRCh38.p7 | 9:98137704 | CTGCAAGACAGTGCC[C/T]AGGAGGGTTGGGGAG | 7464 |
rs199683215 | in-del | -/AAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188774 | GACTCTGTCTCAGAA[-/AAC]AACAACAACAACAAA | 7464 |
rs199709107 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154163 | CTGTCCTCCTTGTCT[-/G]GTTTTGGTATCAAGG | 7464 |
rs199736777 | snp | C/G | 1.65938e-05 | 0.00288039 | intron-variant | CORO2A | GRCh38.p7 | 9:98132340 | ATTGGAGAGACAGTA[C/G]AGGATCGGGGGCAGC | 7464 |
rs199745581 | in-del | -/A | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121441 | AAAAACAGATGGTTT[-/A]AAAAAATATCTGATA | 7464 |
rs199798644 | in-del | -/A | 0.484771 | 0.0859212 | intron-variant | CORO2A | GRCh38.p7 | 9:98189894 | CTCCTTTATTTTTTT[-/A]TTTTTTTTGAGATGG | 7464 |
rs199858774 | in-del | -/TAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164945 | CTCTCCCACCACTAC[-/TAC]CACCACCACCAGGGT | 7464 |
rs199968381 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144302 | TTTACCTCCCAACCA[A/C]CCCAGGACATAGTAC | 7464 |
rs200033483 | snp | C/T | 6.60088e-05 | 0.00574457 | stop-gained | CORO2A | GRCh38.p7 | 9:98133206 | CTTTGTATCCAGGTT[C/T]CAGATCATCACCTGC | 7464 |
rs200053037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133259 | CACAGGGGCCACCTT[A/G]CCCCTGGGCCTCATA | 7464 |
rs200053517 | in-del | -/TA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189889 | GGCAACTCCTTTATT[-/TA]TTTTTTTTTTTTTGA | 7464 |
rs200107116 | in-del | -/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123500 | TCTCTCTCTCTTTTT[-/G]TTTTTTTTTTTTGGA | 7464 |
rs200243300 | snp | A/G | 0.000181194 | 0.00951651 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133119 | CAGGCTGCCGTTGGT[A/G]TTGAAGGACATGGAG | 7464 |
rs200306781 | in-del | -/GA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149947 | TTCTTTTTTTTTTTT[-/GA]GAGAGAGTCTCGCAC | 7464 |
rs200366408 | in-del | -/CTGCCCTGCG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142847 | CTCCCCTGCCCTGCC[-/CTGCCCTGCG]CTGCCCTGCGCTGCC | 7464 |
rs200385626 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145965 | GATCTCCTGCCTTGG[-/C]CTCCCAAAGTGCCAG | 7464 |
rs200393105 | in-del | -/C | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123399 | TGTTTTTCATACTAG[-/C]CCAACATATAAAATA | 7464 |
rs200401293 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176514 | TGTTCCTGGAGCCCC[C/G]CCAGCCACATCCATT | 7464 |
rs200444993 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152139 | CTGTTTTTTTTTTTT[G/T]TTTTTTCTTTAAGGG | 7464 |
rs200464089 | snp | A/C/G | 4.94224e-05 | 0.00497083 | missense, synonymous-codon | CORO2A | GRCh38.p7 | 9:98137596 | TTCAGAACAGGAGGC[A/C/G]ATCTCAAAATCATCA | 7464 |
rs200568168 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139067 | AAAAAAAAAAAGAAA[C/T]AAAAATGCAGAACGA | 7464 |
rs200587871 | snp | C/T | 0.00174846 | 0.0295156 | intron-variant | CORO2A | GRCh38.p7 | 9:98157456 | GGCCTGGGGGTGTCC[C/T]TACCTGGTGCAGGGG | 7464 |
rs200590608 | in-del | -/AGCTGCAGC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192473 | CCCTCCCTCTCCGGG[-/AGCTGCAGC]CGCAGCGCGCACGTC | 7464 |
rs200656917 | snp | C/G | 1.65228e-05 | 0.00287422 | missense | CORO2A | GRCh38.p7 | 9:98132205 | CCCACAAGGCCACCT[C/G]CCGGTTGTTCCATCG | 7464 |
rs200720818 | snp | C/G | 0.000526992 | 0.016224 | missense | CORO2A | GRCh38.p7 | 9:98126659 | TTGGCATCTTCTCCT[C/G]CAACAGGGAGGAAGA | 7464 |
rs200790091 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148810 | CACACACAAAACACA[-/C]AAAAAAAATGATCAA | 7464 |
rs200847195 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177758 | AAGAAAAAAAAAAAA[G/T]AAACTGTGCTCACAC | 7464 |
rs200907246 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124586 | AATTCAGAAACTGTT[A/G]TTGCAAGAAGGCAAA | 7464 |
rs200943565 | snp | A/G | 4.94311e-05 | 0.00497123 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133173 | AATCGTACTCATGGG[A/G]CTTGTGATGACAGAC | 7464 |
rs200947502 | snp | C/G | 1.65291e-05 | 0.00287476 | missense | CORO2A | GRCh38.p7 | 9:98126569 | TCTCTGTCTTTGGTG[C/G]GGGGCATTCGAAAAC | 7464 |
rs200964561 | snp | C/T | 6.62548e-05 | 0.00575526 | intron-variant | CORO2A | GRCh38.p7 | 9:98132317 | CTGGAGGGACACGTG[C/T]GGTCGGTATTGGAGA | 7464 |
rs200969545 | in-del | -/AAAAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188803 | CAAAAAACAACAACA[-/AAAAC]AAAACAAAAGAAACA | 7464 |
rs201025593 | snp | C/T | 6.61299e-05 | 0.00574983 | missense | CORO2A | GRCh38.p7 | 9:98132279 | AGCACTTTGCTGGCC[C/T]GGTGCCCTTTGTAGC | 7464 |
rs201054591 | snp | C/T | 0.000300765 | 0.0122594 | intron-variant | CORO2A | GRCh38.p7 | 9:98130935 | TCCAGGAGGTCACCT[C/T]CCTCCCGTGCCAAGC | 7464 |
rs201065478 | snp | C/G | 8.23784e-05 | 0.00641735 | missense | CORO2A | GRCh38.p7 | 9:98129847 | AGGTAGCTCAGGTGA[C/G]GCTTGTCGGCGCTCA | 7464 |
rs201111862 | snp | C/T | 9.93937e-05 | 0.0070489 | missense | CORO2A | GRCh38.p7 | 9:98128172 | CTGCCTTCCTCACCT[C/T]GATTCATCCCGCTGA | 7464 |
rs201157390 | in-del | -/CCAGAAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181229 | GCACTGCCGGAAAAG[-/CCAGAAC]CCACGGGCACCCACG | 7464 |
rs201163610 | snp | C/T | 0.00399192 | 0.0444975 | intron-variant | CORO2A | GRCh38.p7 | 9:98132131 | GCATGCATGAATGAA[C/T]GACACTGGCTCTCAG | 7464 |
rs201282278 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185275 | GGGCCCTCACGGCTG[G/T]GATGGGTCTAGCTTG | 7464 |
rs201461177 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153694 | CACACACACACACAC[A/T]CACACACACACCCCG | 7464 |
rs201463123 | snp | C/T | 0.00199798 | 0.0315436 | stop-gained | CORO2A | GRCh38.p7 | 9:98137620 | ATCATCAAAAGGGTT[C/T]CACTTGACATCCAAA | 7464 |
rs201468469 | snp | A/G | 6.6166e-05 | 0.0057514 | intron-variant | CORO2A | GRCh38.p7 | 9:98132171 | GATGGTGAGGGGTGG[A/G]GTGCAGCCCTCACCT | 7464 |
rs201511806 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174138 | CCGCCAAAACAAAAA[-/AC]AAAAAAAAAAAACCA | 7464 |
rs201518270 | snp | A/G | 0.000408657 | 0.0142885 | intron-variant | CORO2A | GRCh38.p7 | 9:98134995 | GCAGCATTAGCCAGG[A/G]CACCTTGGCACCGTC | 7464 |
rs201573320 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158408 | TCAACAGTGGCAATC[A/C]CAGCCACTAGTATCA | 7464 |
rs201607824 | in-del | -/GAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150431 | CATTCCCACTCAGGG[-/GAA]TGTTTGCATGTTCTA | 7464 |
rs201681785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156544 | TTATTTAGAAATAGT[C/T]TTTAAGTTTCCAAAT | 7464 |
rs201711318 | snp | C/T | 0.000495229 | 0.015728 | missense | CORO2A | GRCh38.p7 | 9:98133046 | AACTGACCTGGAGGA[C/T]GGTCCCTGCTCGGGG | 7464 |
rs201721099 | snp | A/C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126493 | TCTCAGCCTGGATCT[A/C/G]TTCCCCTCCACCCCA | 7464 |
rs201734917 | snp | A/G | 0.00199792 | 0.0315431 | missense | CORO2A | GRCh38.p7 | 9:98126664 | ATCTTCTCCTCCAAC[A/G]GGGAGGAAGACCTCC | 7464 |
rs201739107 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170938 | CAGAGCTGTCCAGCC[A/G]TCAGCTGTCCTGAGA | 7464 |
rs201778715 | in-del | -/GAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169028 | GGTGGAGGGGTGGGG[-/GAA]GAAGAAGCCCTTTGC | 7464 |
rs201782803 | snp | A/G | 0.000115629 | 0.0076027 | intron-variant | CORO2A | GRCh38.p7 | 9:98137549 | CTTCAGGAAGGGGAA[A/G]CCCCTCAGGGGCTGA | 7464 |
rs201807340 | snp | C/T | 0.000181256 | 0.00951816 | missense | CORO2A | GRCh38.p7 | 9:98157576 | TGCGGGTGATAGGCA[C/T]GGAGTCGTAGCAGTT | 7464 |
rs201854239 | snp | C/T | 6.59098e-05 | 0.00574026 | missense | CORO2A | GRCh38.p7 | 9:98129853 | CTCAGGTGAGGCTTG[C/T]CGGCGCTCACCTCGT | 7464 |
rs201865449 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154333 | TGTGTTTGTGTGTAT[A/G]TATATATATATATAT | 7464 |
rs201915406 | snp | G/T | 0.000197987 | 0.00994758 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126777 | TGCAGGCAGTGGGTG[G/T]GGTCTCAGCAGCTCA | 7464 |
rs202050950 | in-del | -/T | 0.0225045 | 0.103662 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121448 | GATGGTTTAAAAAAA[-/T]ATCTGATAAAAATTA | 7464 |
rs202069747 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160688 | CCGCTCCAGGCCCCC[A/C]CACTCCTCCCTCACC | 7464 |
rs202100203 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164934 | ATAAGTTGGTCACTC[C/T]CCCACCACTACCACC | 7464 |
rs202116728 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | CORO2A | GRCh38.p7 | 9:98149216 | ACTTTTAATTAAAAA[-/G]AAAAAAGCAAAAATA | 7464 |
rs267602332 | snp | A/G | 3.29837e-05 | 0.00406088 | CORO2A | 9 | allele_origin=G(germline)/A(somatic) | 9:98126579 | TGGTGGGGGGCATTC[A/G]AAAACGTCAAAGCCA | 7464 |
rs267602333 | snp | A/G | 1.64727e-05 | 0.00286986 | CORO2A | 9 | allele_origin=G(germline)/A(somatic) | 9:98126667 | TTCTCCTCCAACAGG[A/G]AGGAAGACCTCCAGC | 7464 |
rs367547963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161346 | ATCACTTGAGGTCAG[A/G]AGTTCGAGACCAGCC | 7464 |
rs367559427 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153143 | TTTGCTCTGTCACCC[A/G]GGCTGGAGTGCAGTG | 7464 |
rs367660412 | in-del | -/AA/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167103 | GCAAGATCCTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 7464 |
rs367683956 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | CORO2A | GRCh38.p7 | 9:98126719 | CTGTCTGATTCAAGA[A/G]CCGGGGTGAGGCTGG | 7464 |
rs367722759 | snp | G/T | 3.79226e-05 | 0.00435429 | intron-variant | CORO2A | GRCh38.p7 | 9:98131097 | GAAGGCCTGGGTCAC[G/T]CCTGGGGGCCCTCAG | 7464 |
rs367736265 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150088 | AGGTGGCTGCCACCA[C/T]GCCCAACTAATTTTT | 7464 |
rs367736368 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131772 | CCCTCAAAATACTAC[C/T]GCCAGCTTGGCCCTC | 7464 |
rs367757879 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157210 | AGGAGGAAATAAATT[C/T]GCAGAATTATATTGC | 7464 |
rs367759405 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98169461 | CCCTCTCCCAGGCCA[C/T]GCCAAGGCCTCAGCA | 7464 |
rs367766736 | snp | A/C/G | 4.95711e-05 | 0.0049783 | intron-variant | CORO2A | GRCh38.p7 | 9:98128595 | CTCCCATGCGGTCCC[A/C/G]ACTGCCCTTACCCGC | 7464 |
rs367803653 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194046 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGCAGG | 7464 |
rs367853436 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137437 | CCTCTACCTTAACTT[A/C]ACACCTCCCCACACA | 7464 |
rs367864404 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180103 | TAAACAACGTCAGTG[C/T]GTCAGTGCTAAAACG | 7464 |
rs367902835 | snp | A/G/T | 4.94607e-05 | 0.00497276 | intron-variant | CORO2A | GRCh38.p7 | 9:98129769 | GCTGGGATTACAGGC[A/G/T]TGAACTTCAGTGTCC | 7464 |
rs367905077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98161760 | GGTGGGATCAACCAA[A/G]TGTGGTGCCTGAGTG | 7464 |
rs367961011 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191496 | GGTGAGGGAGGAAGG[A/G]TCAGAGGTTGTTTGT | 7464 |
rs367968563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141274 | CTGTCCTGGCAGGGC[A/G]GTACCTGGAGCTAGG | 7464 |
rs368073137 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163739 | GTGTGTATGTGTGTG[A/T]GTGAGAGAGAGAGAG | 7464 |
rs368094022 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188767 | AGAGCGAGACTCTGT[C/T]TCAGAAAACAACAAC | 7464 |
rs368142515 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130857 | GAGTGGCCAGCGAGG[A/C]CTGCCCATCCCTGCC | 7464 |
rs368153548 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175036 | GCTTTCCTGAACTCC[C/T]TGGCAGCTACATCTC | 7464 |
rs368169601 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141123 | GGGAGAAAGAGAACC[-/A]AAAAAAAAAGGAAAG | 7464 |
rs368175440 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124143 | CTCAGCCTCCCAAGT[C/T]GCTGGAATTACAGGC | 7464 |
rs368248631 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136480 | GCCTTGGCTGCCAGG[C/T]AGCTCTTAGCTAAAC | 7464 |
rs368276546 | snp | A/C/G | 6.59739e-05 | 0.00574305 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128697 | GCAGGAGGACACGTC[A/C/G]AGTCCTCTCTTTGGC | 7464 |
rs368306227 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183883 | CAAGAATCACTTGAA[C/T]CCGGGAGGCGGAGTT | 7464 |
rs368321811 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141817 | TTCTTCCTTGCAGGA[C/T]TGTTGAGAGTTAAAT | 7464 |
rs368323162 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187587 | CCACTTCCTGGGTCA[C/T]AGAATGGCGCCTTCT | 7464 |
rs368331400 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121991 | TAAGACAAGGAACAC[A/G]AGCATCCGGCCTGTG | 7464 |
rs368379383 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153192 | GCAACCCCTGCCTCC[C/T]GGGTTCAAGTGATTC | 7464 |
rs368399056 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172388 | CCAAGCTCAGCCCCA[C/T]ACCCCACTTCTGAGC | 7464 |
rs368493172 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157930 | CCTTTGAGTGTGAAT[A/C]TAACAAGGCAGAAGA | 7464 |
rs368518206 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142790 | TGAGGGAAGGCTGCC[C/T]ACTCACACCCCAGCC | 7464 |
rs368531711 | snp | C/T | | | missense | CORO2A | GRCh38.p7 | 9:98128662 | TTGGTTGTGATCAGC[C/T]TGTAGAAGCGGAAGA | 7464 |
rs368536103 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123620 | CTATCTCAGCCTCCC[A/G]AATAGCAGGGACTAC | 7464 |
rs368548928 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161023 | TGTAGCAGAGCACTT[C/T]CTTCTACTGACATAC | 7464 |
rs368628629 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183757 | TTGAGATCAAGAGTT[C/T]GAGACCAGCCTGGCC | 7464 |
rs368787115 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98161397 | CGTCTCTACTGAAAA[C/T]ACAAAAATTAGCCGG | 7464 |
rs368788938 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172118 | CAGGAGGAAAAGGGT[C/G]TGACTGCCCTGGGAC | 7464 |
rs368790199 | in-del | -/G | 0.00600463 | 0.0544634 | intron-variant | CORO2A | GRCh38.p7 | 9:98130952 | CTCCCGTGCCAAGCC[-/G]ACCTTCCCCACCACG | 7464 |
rs368791212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144901 | CCAATAGAGAGGTGG[A/G]CAAATGGATAGGTGA | 7464 |
rs368806843 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181929 | AAGTCCTATGGCCTC[C/T]CTGAGACTCAGTTTC | 7464 |
rs368825601 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151895 | GATCTCGACTCACTG[C/T]AAGCTCTGCCTCCCG | 7464 |
rs368834482 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | CORO2A | GRCh38.p7 | 9:98144843 | GAGGGGTGAGGCTGA[-/G]GGCATGGAGTCTACT | 7464 |
rs368890494 | in-del | -/TG/TGTG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163730 | GTGTGTGTGTGTGTA[-/TG/TGTG]TGTGTGTGTGTGAGA | 7464 |
rs368921111 | snp | C/T | 0.00156494 | 0.0279289 | intron-variant | CORO2A | GRCh38.p7 | 9:98124921 | CTGGGGAAGAAAGAT[C/T]GGAAGGCAGGATCAC | 7464 |
rs368947037 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157343 | GAAATGACTTACTCA[A/G]GGTCACACAGCTAGT | 7464 |
rs368954246 | snp | A/G | 0.00149526 | 0.0273019 | missense | CORO2A | GRCh38.p7 | 9:98134879 | AGGCCTACTCTGCGC[A/G]CGTGGCCCACGAGTT | 7464 |
rs368959167 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138137 | AAATGAAAAGATAAG[C/T]CCGCAAGAAACTGTT | 7464 |
rs368962513 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98190193 | CCTGGCCAGAAGACA[A/G]CTTCTTACAAATAAC | 7464 |
rs368972483 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174597 | CCTGGTGAGAGGTGA[C/T]TGGATCATGGAGGCG | 7464 |
rs369001554 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174140 | GCCAAAACAAAAAAC[-/AA]AAAAAAAAAACCAAA | 7464 |
rs369027780 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168714 | ACAAGACACTGAGAT[A/G]TGATTTAACACACAA | 7464 |
rs369037410 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145178 | CCACAGCTGGTGTCC[C/T]CACTTGGTCACCTGT | 7464 |
rs369041441 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192484 | CGGGAGCTGCAGCCG[C/G]AGCGCGCACGTCCCG | 7464 |
rs369134629 | snp | C/T | 3.48462e-05 | 0.00417396 | missense | CORO2A | GRCh38.p7 | 9:98130987 | GCATGCTGGTGTCCG[C/T]GTCATAGAAGGGAAA | 7464 |
rs369184780 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131544 | GGCTGGTCTCGAATT[C/T]GTGGCCTCAAGTGAT | 7464 |
rs369203187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139354 | AAAATTAGGCCTGGC[A/G]TGGTGGCTCACGGCT | 7464 |
rs369308454 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98159090 | TTTGAGGAAGGATCT[C/G]GCTCTGTCACCCAGG | 7464 |
rs369326515 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98169171 | GCAAACAGCAAATGC[-/AA]AGAGTCCCGTCCTCA | 7464 |
rs369337310 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170734 | AGGTGTGAGCCACTG[A/G]GCCTGGCCGAGAATC | 7464 |
rs369341535 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151400 | CTATCATTTTCCTTC[C/T]AAGCGTTGCTTGTTT | 7464 |
rs369350824 | snp | C/T | 8.23893e-05 | 0.00641778 | missense | CORO2A | GRCh38.p7 | 9:98157558 | AGTGGTTGTCGTGAA[C/T]GCTGCGGGTGATAGG | 7464 |
rs369356573 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172006 | CGAAGGAAGAAATAA[A/G]TGGGTTTCATTTCAT | 7464 |
rs369391578 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142423 | AGTCCCTGCCCTGGC[C/G]TCCTTCCTGCACACA | 7464 |
rs369479570 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CORO2A | GRCh38.p7 | 9:98130936 | CCAGGAGGTCACCTC[C/T]CTCCCGTGCCAAGCC | 7464 |
rs369543507 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142974 | GCCTGGTGGGCTATT[C/G]ACTGAGCTGCTAAAA | 7464 |
rs369551648 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165823 | ATATCACTAGGGAAC[A/T]TTTTATTTGCAAATT | 7464 |
rs369567605 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174141 | CCAAAACAAAAAACA[A/C]AAAAAAAAAACCAAA | 7464 |
rs369567914 | snp | A/G | 0.000115876 | 0.00761081 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157478 | GTGCAGGGGGATGAC[A/G]AGGAAGGCCCCTCCA | 7464 |
rs369582390 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173614 | CGTCCCAATCCTCCT[C/T]GTCCTCCTTCTCATG | 7464 |
rs369606742 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154707 | AATGATATAGTTTAA[A/G]ATTTGTTTGGCTTAT | 7464 |
rs369615356 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176505 | TGCCCTACCTGTTCC[C/T]GGAGCCCCGCCAGCC | 7464 |
rs369660683 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168317 | TATCTGCCACTCTGG[A/G]CAAGTTACTTAATGT | 7464 |
rs369767635 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132965 | TCACTGTCCTGTTCT[C/T]TGAAGCCTCTCTCTG | 7464 |
rs369792677 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98188539 | GGAGGCCGAGACAAG[C/T]GGATCATTTGAGGTC | 7464 |
rs369811110 | in-del | -/ACAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153650 | CTTCTCTGTTTCCAA[-/ACAC]ACACACACACACACA | 7464 |
rs369849884 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126224 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT | 7464 |
rs369884589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98144081 | GTGGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7464 |
rs369914362 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171478 | GGCAGACCCAGACAG[C/T]GTCACTTATGGGGGA | 7464 |
rs369926939 | snp | C/T | 0.000122013 | 0.00780972 | missense | CORO2A | GRCh38.p7 | 9:98124796 | TGCTCTGAGCCCATC[C/T]GCAAGTTTTTGATCT | 7464 |
rs369935281 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189556 | TTGCTACTGAGATTT[-/G]TTCACTCTAAGAGGT | 7464 |
rs369999602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98172537 | AGATCGACCCCATGC[C/T]TCACTTCCAAGCTCA | 7464 |
rs370021855 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125575 | ATCAAAGTGCCTACC[C/G]CAGGATCTGCCACAC | 7464 |
rs370049521 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127903 | GCTGAGGTGGTCCAG[A/G]CACCCCACATAGCCC | 7464 |
rs370051961 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162206 | GCCTGCAGCTTTTGA[C/G]CCTGCAGCTCCAGGT | 7464 |
rs370064201 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194260 | ATCACTGCACTCCAG[C/T]CTGGGCTACAGAGTG | 7464 |
rs370067313 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150661 | CAAGTTAGAAACAGT[A/G]ACAGTTCTGAGAGTT | 7464 |
rs370084835 | snp | C/T | 3.30644e-05 | 0.00406585 | intron-variant | CORO2A | GRCh38.p7 | 9:98128594 | CCTCCCATGCGGTCC[C/T]GACTGCCCTTACCCG | 7464 |
rs370100438 | snp | A/G | 6.59228e-05 | 0.00574083 | missense | CORO2A | GRCh38.p7 | 9:98157579 | GGGTGATAGGCACGG[A/G]GTCGTAGCAGTTCTC | 7464 |
rs370144250 | multinucleotide-polymorphism | GC/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133904 | GACTACTTGACGCAT[GC/TT]TCCCACACCTGGCTA | 7464 |
rs370146704 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123184 | AGCAACAGATTTCTA[C/T]TCTTTGGGCTGAGAA | 7464 |
rs370152595 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166090 | AAACCCACTGTTGAC[A/C]GAGTCTTTGTATGTA | 7464 |
rs370164427 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133948 | TTTTTGTAGAGATGG[C/G]GTCTCACTATGTTGG | 7464 |
rs370193782 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98140666 | CCCAGGCTGGTCTTG[A/T]ACTCCTGGGCTCAAA | 7464 |
rs370234658 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145225 | CTTCCTCCTGAGGTA[A/G]TTCATCCTACTTTCA | 7464 |
rs370428818 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161442 | GCCTGTAGTCCCAGC[C/T]ACTCTGGAGGCTGAG | 7464 |
rs370430894 | in-del | -/AATA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139646 | ATAAATAAATAAATA[-/AATA]GCCAGGCATGGTGTC | 7464 |
rs370491990 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98163556 | AGGTGGGGATTATTT[G/T]CCCCCATTTGATGAT | 7464 |
rs370538042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162552 | AGGGGGTGGGGCAGC[C/T]GCTAGCAAGGCCAGC | 7464 |
rs370561584 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98169083 | GCAGGGAAGCAGAGC[A/G]CAGCCATCCAGGGAC | 7464 |
rs370569979 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156878 | GGGATCCCTCTAGCC[C/T]CTTCAGGTGTTCTGC | 7464 |
rs370613920 | snp | A/C/T | 3.55412e-05 | 0.0042154 | intron-variant | CORO2A | GRCh38.p7 | 9:98157710 | TCACTGCCCTGATCA[A/C/T]GGGACACACAGAGCT | 7464 |
rs370621949 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139567 | AGGAGGTGGAGGTTG[C/T]GGTGAGCTGAGATTG | 7464 |
rs370704573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160354 | GCAGGAGGAGTTAAG[C/T]TAGGTGTGCGGCCAG | 7464 |
rs370867876 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98137293 | ATGGGTTTTCCCATC[A/G]GAATATACATTTTCA | 7464 |
rs370924521 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193494 | GCTCCCACGGCTACT[A/G]AGCTAACAGCCACTC | 7464 |
rs370931557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98174982 | ATTAAAAAAATAATA[A/G]AGAAAAGAGAAATGA | 7464 |
rs370955308 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98161410 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGCG | 7464 |
rs371007562 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | CORO2A | GRCh38.p7 | 9:98168839 | GAGAGTTCCAACCCC[C/T]GGTGCAAACCATGAT | 7464 |
rs371084777 | snp | C/G/T | 8.29007e-05 | 0.00643773 | synonymous-codon, missense | CORO2A | GRCh38.p7 | 9:98126561 | CACCTCATTCTCTGT[C/G/T]TTTGGTGGGGGGCAT | 7464 |
rs371139869 | snp | A/G | 1.66078e-05 | 0.00288161 | missense | CORO2A | GRCh38.p7 | 9:98134948 | TTGGGGATGCTCCAG[A/G]TCTTAATCTGGCAGG | 7464 |
rs371192075 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98169425 | CCAGCCCTGCCCCCA[C/T]GGCCCCCACCTGCTC | 7464 |
rs371210517 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133753 | GGTTCCCTCAGTGCT[A/C]CCCACAACAATTTTA | 7464 |
rs371225634 | snp | G/T | 6.59435e-05 | 0.00574172 | missense | CORO2A | GRCh38.p7 | 9:98157597 | CGTAGCAGTTCTCCT[G/T]GCTGGCTGGTTTGCC | 7464 |
rs371227963 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164830 | GTAGGGCAACTAACT[C/G]TCTTGGTTTGCCTCG | 7464 |
rs371233180 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129128 | GGAGTCTCACTTTGT[C/T]GCCCAGGCTAGGCTC | 7464 |
rs371297558 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161363 | GTTCGAGACCAGCCT[A/G]GCCAACATGGTGAAA | 7464 |
rs371315981 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130529 | AGAACTGGGGTGGCC[C/T]CAGAGGTCATCCAGA | 7464 |
rs371477135 | snp | C/G | 0.000115398 | 0.00759512 | intron-variant | CORO2A | GRCh38.p7 | 9:98137722 | GAGGGTTGGGGAGGA[C/G]GTGGATTCCACATTA | 7464 |
rs371481433 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189377 | AATTATTTTCTGGAC[C/T]TCCTGAGATTTGGCA | 7464 |
rs371523682 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132464 | GGGCACCACCTGGAT[C/T]CCTCTCATCCACATG | 7464 |
rs371553593 | snp | A/G | | | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172685 | CAGTTCCCCAGGCAG[A/G]GTCTGCAACAGCTGG | 7464 |
rs371564240 | snp | C/T | 1.65888e-05 | 0.00287996 | intron-variant | CORO2A | GRCh38.p7 | 9:98132338 | GTATTGGAGAGACAG[C/T]AGAGGATCGGGGGCA | 7464 |
rs371597213 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163741 | GTGTATGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 7464 |
rs371613586 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155491 | AGCTGGGATTACAGG[A/T]GCCCGCCACTGTGCC | 7464 |
rs371674759 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98170831 | TTCTATCCATATAAT[A/G]GTAACAGCCCTGCCC | 7464 |
rs371693595 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161424 | CCGGGTGTGGTGGCG[C/T]GCGCCTGTAGTCCCA | 7464 |
rs371702615 | snp | C/G | 1.64768e-05 | 0.00287021 | missense | CORO2A | GRCh38.p7 | 9:98129801 | TCACTTACCGATCCC[C/G]TTCTGTGGGTTATAG | 7464 |
rs371707565 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98169503 | TGGGGACTCAGGCCT[C/T]GCATATTCCACCCCC | 7464 |
rs371812636 | snp | C/T | 2.86578e-05 | 0.00378525 | missense | CORO2A | GRCh38.p7 | 9:98124841 | TTGGCCTGGACCTCT[C/T]GCTGGGTCAACAGCT | 7464 |
rs371817356 | snp | A/C | | | splice-donor-variant | CORO2A | GRCh38.p7 | 9:98137571 | AGGGGCTGACACTCA[A/C]TGTGGCATCTTCAGA | 7464 |
rs371917817 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124043 | TTTGAGACAGACTTT[C/T]GCTCTTATTGCCCAG | 7464 |
rs371927565 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186031 | GGCCCAGGGAACACA[C/T]GCCTGCCCCTGCACT | 7464 |
rs371962738 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180392 | AAGCATTCCCATCCA[A/T]CCCCTCGCAGGCCAT | 7464 |
rs372039529 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175585 | GGGCATGGGCATCCC[C/T]GCCTGTCACCTTCCA | 7464 |
rs372047609 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159277 | TGGTCTCAACCTCCT[A/G]ATCTCAAGCAATTCT | 7464 |
rs372057573 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142856 | CCTGCCCTGCCCTGC[C/G]CTGCCCTGCGCTGCC | 7464 |
rs372169689 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145572 | TGAGGTTCCAAACAG[C/T]TGGCTAGGACAGGGC | 7464 |
rs372188925 | snp | A/C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161109 | CATGGAGGACAGCGA[A/C/G]CCATCCTGATTCATA | 7464 |
rs372192509 | snp | A/G | 3.30055e-05 | 0.00406222 | intron-variant | CORO2A | GRCh38.p7 | 9:98129749 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 7464 |
rs372221577 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189893 | AACTCCTTTATTTTT[A/T]TTTTTTTTTGAGATG | 7464 |
rs372226971 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138368 | GTGAGCTCTGATTGC[A/G]CCATTGCACTCCAGC | 7464 |
rs372343323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146183 | TTGCTTTCATTCCTC[A/C]CCACCCTCCACACCT | 7464 |
rs372354083 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192130 | AGGCCCAGCAGGTAA[C/G]GCAGCCAAGAGGGGG | 7464 |
rs372388067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144959 | TGTGGGACCAGGGAC[C/T]GCCCAGAGGAGGCTG | 7464 |
rs372389188 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124170 | AGGCGCCTGCCACCA[C/G]GCCCAGCTAATTTTT | 7464 |
rs372493952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134256 | GGAATAGAATTGAGG[A/T]CTCCTGTACTGTGGG | 7464 |
rs372665626 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98155195 | ATTTTCTTTGCTATG[-/TT]AAGTGCTGGTTCAGT | 7464 |
rs372692843 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162547 | AAGTAGGGGGTGGGG[-/C]CAGCCGCTAGCAAGG | 7464 |
rs372696837 | in-del | -/GGCACCCCCACCCCACTTCTGAGCTC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172209 | CCCACTTCTGAGCTC[-/GGCACCCCCACCCCACTTCTGAGCTC]AGCCCCACGCCCTAC | 7464 |
rs372708640 | in-del | -/CACT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153691 | ACACACACACACACA[-/CACT]CACACACACACCCCG | 7464 |
rs372739932 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | CORO2A | GRCh38.p7 | 9:98138844 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCC | 7464 |
rs372861931 | snp | A/G | 6.83258e-05 | 0.00584451 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134842 | GAAGAGGATGTTGGC[A/G]GCCGTGGGGTGCCAC | 7464 |
rs372930440 | snp | A/C | 2.07256e-05 | 0.00321906 | intron-variant | CORO2A | GRCh38.p7 | 9:98130940 | GAGGTCACCTCCCTC[A/C]CGTGCCAAGCCGACC | 7464 |
rs372968536 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171126 | GACACCTCCAGGAGG[C/G]TGAAAATCTGGCAGC | 7464 |
rs373005604 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126585 | GGGGCATTCGAAAAC[A/G]TCAAAGCCATTTGTC | 7464 |
rs373087105 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140103 | AACAGGGACCAGGAC[C/G]CAGGCCCTCGACCTC | 7464 |
rs373091886 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152156 | TTTTTCTTTAAGGGA[A/C]ATTTTTATTGCTCAA | 7464 |
rs373104710 | snp | C/T | 0.000160418 | 0.00895451 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98131012 | GGGAAACAGCACGCC[C/T]GAGGAGCCGTCCAGG | 7464 |
rs373187113 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132678 | AGAAAACAGAGGCTC[A/G]GAGCAGGAAGCGCTT | 7464 |
rs373209904 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140006 | GGGGTCATAGAGAAA[C/T]CACACCAGTTCAGTC | 7464 |
rs373274605 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176977 | TTTTGTTCCTTATCT[A/G]TGTTGCTCTAAGTAA | 7464 |
rs373279032 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151068 | ACCTCCATGCCTTTG[C/T]TTGTGCCCTTCCCTT | 7464 |
rs373319617 | snp | A/G | 4.04703e-05 | 0.00449817 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124734 | CCTCCCCATGGAGCC[A/G]AGTGGTGTCCCTGAG | 7464 |
rs373402442 | snp | A/C | 0.000307953 | 0.0124049 | intron-variant | CORO2A | GRCh38.p7 | 9:98157423 | CTCTGTCCTGCCCTG[A/C]CTCCAGAGAGCTGTT | 7464 |
rs373478798 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146188 | TTCATTCCTCCCCAC[C/T]CTCCACACCTCACAG | 7464 |
rs373553898 | snp | G/T | 3.4205e-05 | 0.00413537 | intron-variant | CORO2A | GRCh38.p7 | 9:98157667 | CCATGACATCTGCAG[G/T]AGACAAATGGGACAA | 7464 |
rs373556235 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161447 | TAGTCCCAGCCACTC[G/T]GGAGGCTGAGGCAGG | 7464 |
rs373607602 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123285 | ACAAATATCACTTGC[C/T]TCTCTCTAGGCCTTA | 7464 |
rs373619389 | snp | C/G | 1.65081e-05 | 0.00287293 | intron-variant | CORO2A | GRCh38.p7 | 9:98128600 | ATGCGGTCCCGACTG[C/G]CCTTACCCGCCGGGG | 7464 |
rs373647567 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123678 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 7464 |
rs373658313 | snp | A/G | 6.72597e-05 | 0.00579873 | intron-variant | CORO2A | GRCh38.p7 | 9:98128122 | GGGGCCACTGGGCAC[A/G]CCATGTTCCTGTCAC | 7464 |
rs373658669 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163194 | ACTGAGTTTATTTCT[C/T]TTTTTTTCTTTGAGA | 7464 |
rs373704777 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145417 | GAAGACAGAGGACCC[A/G]TTCCTTGAGTATGTT | 7464 |
rs373733956 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | CORO2A | GRCh38.p7 | 9:98126670 | TCCTCCAACAGGGAG[A/G]AAGACCTCCAGCCAT | 7464 |
rs373743222 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149950 | CTTTTTTTTTTTTGA[C/G]AGAGTCTCGCACTGT | 7464 |
rs373924781 | snp | A/G | 0.000131776 | 0.00811608 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137638 | CTTGACATCCAAAAC[A/G]TTGCCTCTGTGCCCG | 7464 |
rs373953546 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131330 | CCCTTAACAAATCAC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs373963549 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155448 | GCCTCCTGCGTTCAA[A/G]CAATTCTCCTGCCTC | 7464 |
rs373976722 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181653 | CAGTTCTTCAAAGTC[C/T]TGTTTCCTCCAGCCG | 7464 |
rs373982265 | in-del | -/GAAG | 0.00993419 | 0.0697739 | intron-variant | CORO2A | GRCh38.p7 | 9:98169031 | GGAGGGGTGGGGGAA[-/GAAG]GAAGCCCTTTGCTTT | 7464 |
rs374013776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98170094 | TCTAGAAGATTAAAT[G/T]AAATAATGTATGTAA | 7464 |
rs374047574 | in-del | -/GTT | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194441 | AACTTTGTTGTTGTT[-/GTT]TTTGCATGGTTTTGT | 7464 |
rs374221627 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98184637 | TGCTTTGGGTCTGAC[A/G]TTGTTCCTCCTCATC | 7464 |
rs374223018 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129353 | TTACTTTTAATCTAG[C/T]CATGTCTTTATGTTT | 7464 |
rs374227832 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160262 | AAATAGAACACAAGA[C/T]AGAAGGAAATGAAAA | 7464 |
rs374251510 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130558 | GAAGGTCTTACCATG[C/G]GGAACATTTCTGGTT | 7464 |
rs374273495 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144121 | TTGAGCCTGGGAGGT[C/G]CAGCCTACAGTGAGC | 7464 |
rs374297648 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98172090 | GAATTCTGAGGCCTT[C/G]CGTGCTTGGACTCAG | 7464 |
rs374306151 | in-del | -/AA | 0.427119 | 0.176434 | intron-variant | CORO2A | GRCh38.p7 | 9:98148098 | TTAAAAAAAAAAAAG[-/AA]AAAAAAAAAAAGAGG | 7464 |
rs374355516 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152904 | CTGAATTGGATTCTA[G/T]ATCAGAAAAAAAAGC | 7464 |
rs374389147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145762 | CTGTCGCCCAGGCTG[G/T]AGTGCAATGGTGCGA | 7464 |
rs374402648 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125883 | CCACCATACCCAGCT[A/G]ATTTTTGTATTTTTA | 7464 |
rs374417724 | snp | C/T | 3.31945e-05 | 0.00407383 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157628 | AAAGACATGACGGAA[C/T]TTGGAGCTCCGGTAC | 7464 |
rs374467650 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172197 | GAAGCCCCACACCCC[A/G]CTTCTGAGCTCGGCA | 7464 |
rs374469951 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185703 | TTGCCCAGTTATTGA[A/G]CACGCCATAGACCAC | 7464 |
rs374505837 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126759 | ATTGAAGATAGGTCT[C/T]TCTGCAGGCAGTGGG | 7464 |
rs374508656 | snp | C/T | 1.66349e-05 | 0.00288395 | intron-variant | CORO2A | GRCh38.p7 | 9:98132346 | GAGACAGTAGAGGAT[C/T]GGGGGCAGCTGGGGT | 7464 |
rs374532010 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191878 | ACCAGCACCTGGCCC[A/G]GGTGGGGAAGGGGAA | 7464 |
rs374544693 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174690 | TGGCAGTTTCCCCTG[C/T]GAGTTATCTCCCTCC | 7464 |
rs374548130 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142616 | AGTCAGGCTGCCCTC[A/G]GGCTGACGGGAGGCA | 7464 |
rs374561747 | snp | C/T | 0.00107354 | 0.0231434 | missense | CORO2A | GRCh38.p7 | 9:98132207 | CACAAGGCCACCTGC[C/T]GGTTGTTCCATCGGG | 7464 |
rs374579922 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164488 | TGGAGGATAAGGCCA[A/C]CCTGCTGCCAACCTA | 7464 |
rs374600440 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169702 | TCCCCTCAAAGCATC[A/G]TGCTTTTCAAAAGAG | 7464 |
rs374755033 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177457 | TGGGCTCCAAACTTT[-/G]TTTTTTTTTTTTTTT | 7464 |
rs374813149 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175161 | GGGTGGGGTGCGGGA[A/T]GGCCCTCCCTGTCTG | 7464 |
rs374814331 | snp | C/T | 7.18649e-05 | 0.00599394 | missense | CORO2A | GRCh38.p7 | 9:98130966 | CGACCTTCCCCACCA[C/T]GTAGAGCATGCTGGT | 7464 |
rs374900725 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98137763 | AGTCACATAGTCAGT[G/T]AGCAACCAGTCAACA | 7464 |
rs374945688 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171982 | CTTTCCTCAACTTTG[A/G]GCTGGTATCGAAGGA | 7464 |
rs374959179 | snp | A/C | | | missense | CORO2A | GRCh38.p7 | 9:98126757 | GAATTGAAGATAGGT[A/C]TCTCTGCAGGCAGTG | 7464 |
rs374973997 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98182270 | AACTTTTTAGGGAGC[A/G]AATGAATGGGTCAGT | 7464 |
rs374974856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98138905 | ACAAAAAATTAGCCC[A/G]GCGTGGTGGTGCACG | 7464 |
rs375084086 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133092 | CTTGCGGTCTTTGCA[A/G]GTGGTGGCCAACAGG | 7464 |
rs375122072 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194037 | TCATGCTTGTAATCC[C/T]AGCACTTTGGGAGGC | 7464 |
rs375155659 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98158245 | GAGCCCAGGAGTTCA[A/C]ATGTAGCCTGGGCAA | 7464 |
rs375160539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98159685 | AAGTAGCAGAGATCT[C/T]GCTCTCCTCTGTTCC | 7464 |
rs375182845 | snp | A/G | 0.000153988 | 0.00877328 | missense | CORO2A | GRCh38.p7 | 9:98128692 | ATCTCGCAGGAGGAC[A/G]CGTCGAGTCCTCTCT | 7464 |
rs375207574 | snp | A/G | 4.94539e-05 | 0.00497238 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157535 | GAAGTGGGGGTTCAC[A/G]GCACAGAAGTGGTTG | 7464 |
rs375263389 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO2A | GRCh38.p7 | 9:98146616 | GATACATCTCTGTGC[C/T]TGGCACAGAACGTAA | 7464 |
rs375269323 | snp | C/T | 0.000149116 | 0.00863342 | missense | CORO2A | GRCh38.p7 | 9:98157477 | GGTGCAGGGGGATGA[C/T]GAGGAAGGCCCCTCC | 7464 |
rs375298275 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98135585 | GTTGTCTGAAGATGG[A/G]GGGGGCTGCCATGGC | 7464 |
rs375299108 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172615 | GGAAGTTCTTTTCCG[C/T]TACTCTCTCACCTGC | 7464 |
rs375326249 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191099 | GGTGCAGGGCAGGTC[A/C]TGAAGGGGACAAGAA | 7464 |
rs375328122 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137382 | GCCCATAGAGAGGAG[C/G]GGTGGTGCCGCTAGT | 7464 |
rs375331830 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CORO2A | GRCh38.p7 | 9:98166976 | GGGCATGGTGGCACA[C/T]ACCTGTAGTCCCAGC | 7464 |
rs375458218 | snp | A/G | 8.27959e-05 | 0.00643359 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126816 | CCTAAGGGACACCAG[A/G]ATTGGGTCTGGAAGG | 7464 |
rs375495395 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98141139 | AAAAAAAAAGGAAAG[A/G]ATGTGGACTTGTGTC | 7464 |
rs375511133 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | CORO2A | GRCh38.p7 | 9:98189665 | AGGGGAACGGATCGG[A/C]CCAAGGTCACACAGT | 7464 |
rs375512806 | in-del | GA/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149947 | TTTCTTTTTTTTTTT[GA/T]GAGAGAGTCTCGCAC | 7464 |
rs375515622 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CORO2A | GRCh38.p7 | 9:98132321 | AGGGACACGTGCGGT[C/T]GGTATTGGAGAGACA | 7464 |
rs375627893 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156520 | TTGATTTTGTTTATG[A/G]CCTATAAATTATTTA | 7464 |
rs375635134 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98161243 | CTGAGGGCAGTGGGG[-/A]GCTACTGGAGAAATT | 7464 |
rs375671314 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CORO2A | GRCh38.p7 | 9:98134959 | CCAGATCTTAATCTG[A/G]CAGGGGAGACAGGGC | 7464 |
rs375732883 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174071 | GAGATTGCGCCATTG[A/C]ACTCCAGCCTGGGCA | 7464 |
rs375771898 | snp | A/G | 0.000264883 | 0.0115053 | intron-variant | CORO2A | GRCh38.p7 | 9:98128589 | ACCTGCCTCCCATGC[A/G]GTCCCGACTGCCCTT | 7464 |
rs375835521 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144885 | GGGTGCAAGGCTGGA[C/T]CCAATAGAGAGGTGG | 7464 |
rs375886428 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165974 | AATACCTGAACCCAC[C/T]GCCCAATCTTAGCAT | 7464 |
rs375892568 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CORO2A | GRCh38.p7 | 9:98151963 | CTGGGACCACAGGCG[C/T]ACGCCACCATGCCCG | 7464 |
rs375934298 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174139 | CGCCAAAACAAAAAA[A/C]AAAAAAAAAAAACCA | 7464 |
rs375971591 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163201 | TATTTCTTTTTTTTT[-/T]CTTTGAGACGGAGTC | 7464 |
rs375976863 | snp | C/T | 6.11154e-05 | 0.00552756 | missense | CORO2A | GRCh38.p7 | 9:98124889 | TCCTCCTGTTGCCGG[C/T]AGAACATCTGCAGCA | 7464 |
rs376011943 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189297 | GTGATTGCAAAGCAC[A/G]TCCAATCTGTTCTGA | 7464 |
rs376036915 | snp | A/G | 0.000139502 | 0.00835053 | missense | CORO2A | GRCh38.p7 | 9:98130986 | AGCATGCTGGTGTCC[A/G]CGTCATAGAAGGGAA | 7464 |
rs376102288 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140665 | GCCCAGGCTGGTCTT[A/G]AACTCCTGGGCTCAA | 7464 |
rs376104854 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154362 | ATATATACACAAATA[C/T]ATATATATATATATT | 7464 |
rs376126684 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168692 | GATTGTTGTGGTCCC[A/C]ATGTGTACAAGACAC | 7464 |
rs376234232 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169781 | TCTGTCTTTGCTCAT[A/G]CCCCTTCCCTCTGCC | 7464 |
rs376239065 | in-del | -/A | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173016 | CACCTGGAGGGCTGG[-/A]AAAAAACAAACCCAG | 7464 |
rs376289669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98160023 | GTCATAGCGATAAGG[A/G]CCTGACCCCTGAGGC | 7464 |
rs376364338 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148802 | CAAAACACACACACA[A/C]AAAACACAAAAAAAA | 7464 |
rs376408996 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123030 | AGGTAGTTTTCTCTT[A/T]GGTCAAGGTTTCAGG | 7464 |
rs376416026 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191999 | TAGGGCTCCTCCAGC[A/C]CCAGACGAGTAAACC | 7464 |
rs376535111 | in-del | -/AAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180093 | CCTGCAATTCTAAAC[-/AAC]GTCAGTGCGTCAGTG | 7464 |
rs376561288 | snp | A/T | 0.000154925 | 0.00879992 | intron-variant | CORO2A | GRCh38.p7 | 9:98157675 | TCTGCAGGAGACAAA[A/T]GGGACAAAGGGTATG | 7464 |
rs376566115 | snp | C/T | 0.000529458 | 0.0162619 | missense | CORO2A | GRCh38.p7 | 9:98124886 | ATCTCCTCCTGTTGC[C/T]GGTAGAACATCTGCA | 7464 |
rs376643877 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147739 | CTTATAAGGCTAAAC[A/C]TGCAACTACCTTATG | 7464 |
rs376663666 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131532 | CTGTGTAGCTCAGGC[C/T]GGTCTCGAATTCGTG | 7464 |
rs376665698 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149993 | ATGGAGTGCAGTGGC[A/G]CGATCTTGACTCACT | 7464 |
rs376733891 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132550 | AAACTTCTGCCCAGC[A/G]CCCTGTTCTTGCTGA | 7464 |
rs376777438 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166997 | TAGTCCCAGCTACTC[A/G]GGAGGTCAAGGTGGG | 7464 |
rs376781378 | snp | A/C/T | 0.000478082 | 0.0154537 | intron-variant | CORO2A | GRCh38.p7 | 9:98129765 | AAGTGCTGGGATTAC[A/C/T]GGCATGAACTTCAGT | 7464 |
rs376852992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98181703 | TTTCTCCTATGCAGC[A/G]TGCCTCCCTCCCCAC | 7464 |
rs376879410 | snp | C/T | | | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172729 | TGAGGTACCTCCTCT[C/T]TGCTTCCAGCCTCCA | 7464 |
rs376880021 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126118 | TTGGCTCACTGCAAC[A/C]TCCACCTCCCAATTT | 7464 |
rs376884560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146217 | AGCAAAGTCCACCTT[C/T]TTCACCCCCTCCCTG | 7464 |
rs377036622 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156309 | CCTTCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 7464 |
rs377039626 | in-del | -/TGTATA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154328 | TCTTATGTGTTTGTG[-/TGTATA]TATATATATATATAT | 7464 |
rs377042279 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157244 | GAAGAGGAGAGGTGC[C/T]ACGAGTAGCTAAGCC | 7464 |
rs377101922 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145143 | TGTAGAATCCAACAT[C/G]CAGGGATGAAAGCGG | 7464 |
rs377238503 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163120 | ATGGGATTAGGCTCC[A/G]GGGCCTGTGAATTCC | 7464 |
rs377256694 | in-del | -/CAGACGGTCC | 0.324855 | 0.23853 | intron-variant | CORO2A | GRCh38.p7 | 9:98191249 | TCACTCCGGACCTCT[-/CAGACGGTCC]CCAGGAGGGGCAGGA | 7464 |
rs377262244 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178643 | GACTCCTGGACCACA[C/T]GAGACAGGAGACTCC | 7464 |
rs377336075 | snp | A/G | 2.00038e-05 | 0.00316251 | missense | CORO2A | GRCh38.p7 | 9:98124787 | GCTCAGAGCTGCTCT[A/G]AGCCCATCCGCAAGT | 7464 |
rs377461816 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161414 | CAAAAATTAGCCGGG[C/T]GTGGTGGCGCGCGCC | 7464 |
rs377490116 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143869 | TACTGGTGAATGCAG[C/G]CAGCTGGATCAGACA | 7464 |
rs377513173 | snp | C/G | 3.39046e-05 | 0.00411718 | intron-variant | CORO2A | GRCh38.p7 | 9:98128747 | AGGGAGGGCCAAGAG[C/G]TTCTGGCTAGGCTGG | 7464 |
rs377563262 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134457 | TGGAAATGGGGTCTT[C/T]GCTGCTGAAATTAGT | 7464 |
rs377574369 | in-del | -/GA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149216 | ACTTTTAATTAAAAA[-/GA]AAAAAGCAAAAATAA | 7464 |
rs377590670 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193862 | GCTCCCTGCCTACCA[C/T]CCAAAGCCCAGTGTG | 7464 |
rs377597653 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141621 | GGCCTTCCAAAGTGC[C/T]GGGATTATAGGCTTG | 7464 |
rs377606628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98169016 | GGACCTGGGACGGGG[C/T]GGAGGGGTGGGGGAA | 7464 |
rs377629153 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144500 | ACATACTATGTGCCA[G/T]ACTGCATGCAGGTGA | 7464 |
rs377642653 | snp | C/T | 5.16685e-05 | 0.00508248 | intron-variant | CORO2A | GRCh38.p7 | 9:98135006 | CAGGGCACCTTGGCA[C/T]CGTCACCAGCCTAAG | 7464 |
rs377672464 | snp | C/T | 1.6972e-05 | 0.00291303 | missense | CORO2A | GRCh38.p7 | 9:98157658 | CTGGGGGTGCCATGA[C/T]ATCTGCAGGAGACAA | 7464 |
rs377675370 | snp | A/G | 3.30469e-05 | 0.00406477 | missense | CORO2A | GRCh38.p7 | 9:98132208 | ACAAGGCCACCTGCC[A/G]GTTGTTCCATCGGGA | 7464 |
rs377703706 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155626 | CTGGGATTAAAGGCA[C/T]GAGCCACCACGCCTG | 7464 |
rs377735244 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121591 | GTCTGGGTCCCTTGG[C/G]GTGGAGGGAGCTGGC | 7464 |
rs377738674 | snp | C/T | 3.30961e-05 | 0.0040678 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134926 | GAGGTTCCTGGTCAG[C/T]AGCTGCTTGGGGATG | 7464 |
rs386415588 | in-del | -/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156066 | TTTTTTTTTTTTTTT[-/TTT]TTGAGACAGGGTCTC | 7464 |
rs386415589 | in-del | -/ATGTACCA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165112 | AGCTAAGAACAAGCA[-/ATGTACCA]TGTACCACCGTGCTT | 7464 |
rs386415590 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167117 | CAAAAAAAAAAAAAA[-/AAA]AAGAAAGAAAAGAAA | 7464 |
rs386736660 | in-del | CC/GAATG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150431 | CATTCCCACTCAGGG[CC/GAATG]TTTGCATGTTCTATT | 7464 |
rs386736661 | multinucleotide-polymorphism | GAC/TAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162078 | CTTTCCATGCATGAA[GAC/TAG]AGCAAGTGGGTGCTA | 7464 |
rs386736662 | in-del | AAC/TGCCGGAAAAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181233 | TGCCGGAAAAGCCAG[AAC/TGCCGGAAAAG]CCACGGGCACCCACG | 7464 |
rs386736663 | in-del | AA/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183175 | TCAGAAAGCGGCCCA[AA/G]CTTCAGCAGGACCCT | 7464 |
rs386736664 | multinucleotide-polymorphism | ATA/GTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184768 | ATCAAGGGGTGTGTG[ATA/GTT]AATGGCGGCTGTCTG | 7464 |
rs386736665 | in-del | AGACGGTCCCCAG/CA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191250 | CACTCCGGACCTCTC[AGACGGTCCCCAG/CA]GAGGGGCAGGAAGCT | 7464 |
rs397686614 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189707 | GACTTCAATCTGGAA[-/A]TCTATGTCTGCTGAC | 7464 |
rs397748600 | in-del | -/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152138 | CTGTTTTTTTTTTTT[-/TTT]GTTTTTTCTTTAAGG | 7464 |
rs397753329 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148534 | ACTTAAGCCCAGGGG[-/G]TTCAAGACCAACCTG | 7464 |
rs397805919 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173548 | TGCTTTCTTAAGTCT[-/T]CTTCTCAACATATAA | 7464 |
rs398011596 | in-del | -/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98127845 | CTACCTCTGCAATTC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs398046655 | in-del | -/A | 0.5 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98166954 | GAAATAAAAAAAAAA[-/A]TTAGCTGGGCATGGT | 7464 |
rs398113697 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141948 | ACTGAGAAAAAAAAA[-/A]CTAAAAGGAATGAGC | 7464 |
rs527259250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176127 | AAGATCTAAACATTC[A/G]GCGGGGGGTGAGGGG | 7464 |
rs527260905 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184965 | TTTATCCAATTTAGA[A/G]CCTTACAACAAGCTT | 7464 |
rs527264251 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138578 | AGAGGAATGAAGTAC[C/G/T]GGTCCCTGCTACAGC | 7464 |
rs527284223 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166891 | GGATCGCTTGGGTTC[C/T]GGAGTTCAAGACCAG | 7464 |
rs527406337 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98144813 | GAGGACAGGGCAAGA[A/G]AGGAGGCTGAGCAAG | 7464 |
rs527413569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187573 | AGTCTGGTGAGGGCC[C/G]ACTTCCTGGGTCATA | 7464 |
rs527596691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98163224 | ACGGAGTCTCGCTCT[A/G]TTGCCCAGGCTGGAG | 7464 |
rs527632414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98162793 | CGCATGCGTGTATCC[A/G]TGCATGCATGACTTT | 7464 |
rs527744315 | snp | A/C/T | 0.000428347 | 0.0146286 | missense | CORO2A | GRCh38.p7 | 9:98129857 | GGTGAGGCTTGTCGG[A/C/T]GCTCACCTCGTAGTA | 7464 |
rs527808801 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136356 | CAGCATCTGCTATAT[A/G]GAAACCGACACAAAT | 7464 |
rs527828115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136899 | CACTATGTTGCCTAG[A/G]TTGGTCTCCAACTCC | 7464 |
rs527854176 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194145 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCATGT | 7464 |
rs527865793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135791 | TCAGCAAATATTTAT[C/T]TCCTGGTCATCTTGG | 7464 |
rs527891555 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181437 | TGTCTCAGTCTCCCA[A/G]AGTGCTAGGATTATA | 7464 |
rs527951087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142651 | GCCCAGGAGCCCCAT[G/T]CAGACACACACCTCC | 7464 |
rs527979841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186152 | CAAATGCTCAGCTCC[C/T]GATTTCTTATTTGAA | 7464 |
rs528001643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98192551 | CCGGCGGCGCAGGGC[C/T]GCCCTACCTTGATGA | 7464 |
rs528033946 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160851 | ATGACCCGTTAGCCA[C/G]TGGATCATGGGAGGC | 7464 |
rs528056988 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186840 | CTCATCCTCCTCCTG[C/T]TCACCTGGCCTGGAC | 7464 |
rs528113433 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168181 | TTCAAGAGCTCAAAA[A/G]CCACATGTGCTTCAT | 7464 |
rs528146850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126934 | GAGCCATGCAGACCC[A/G]TGCAACATGTGTGGG | 7464 |
rs528168852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172269 | GAGCTCAGTCCCACA[C/T]CCCACTTCTGAGCTC | 7464 |
rs528212315 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147748 | CTAAACATGCAACTA[C/T]CTTATGACTCAGCAA | 7464 |
rs528218578 | snp | C/G/T | 3.42362e-05 | 0.00413729 | intron-variant | CORO2A | GRCh38.p7 | 9:98126531 | CATGTGAAAGGCCCA[C/G/T]CCCGTCCTCCTTCAC | 7464 |
rs528240218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98171820 | CTGCCGCTGGGAGAG[A/G]TGCTGGGGGCGCAGT | 7464 |
rs528257407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140449 | CTGTACTTGTTTTTT[A/T]TTTTTTTAAGAGACA | 7464 |
rs528298590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184272 | TCTTACTTTGTTGCC[C/T]AGGCTGGTCTCAAAC | 7464 |
rs528298876 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98177635 | CCACACCCGGCAAAT[G/T]TTTTTGTATTTTTAA | 7464 |
rs528333794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165099 | TCAGCCTCCTGCATA[A/G]CTAAGAACAAGCATG | 7464 |
rs528344607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140000 | TTTCTTGGGGTCATA[C/G]AGAAACCACACCAGT | 7464 |
rs528372555 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188414 | CTTTGGGGGAAGATC[C/T]TTCTGGTCTATTTTG | 7464 |
rs528428755 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158852 | ACACACACACACACA[C/T]ACACACACCATGTAT | 7464 |
rs528453808 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173378 | GGATTATCTCCACTT[C/T]GTGAGTGTGGCCGGG | 7464 |
rs528471749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98146471 | TGCCTGGGGCAGCCC[A/G]GCCCCTCTGAGAAGG | 7464 |
rs528482799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153210 | GTTCAAGTGATTCTC[C/T]TGCCTCAGACTCCTG | 7464 |
rs528487802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189337 | GGCATGGATTATAGA[A/C]TTAAAACACAAGAAG | 7464 |
rs528613046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98159775 | TCAGGGTCAGTTCTC[A/G]TTTTCTCTGCTGGCT | 7464 |
rs528618647 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159654 | ACTTCCTCCAGAGAG[C/T]CCTCCTTGATATCCC | 7464 |
rs528630141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132764 | GCCAGAGCTGAGGCA[C/T]GCCAACAAGCTTTGG | 7464 |
rs528705399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125484 | TCAGAATCCATCTGT[A/G]AGATGCCAGCCTCTG | 7464 |
rs528716794 | in-del | -/TT/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156050 | GCTCTTTGTTTGAAT[-/TT/TTT]TTTTTTTTTTTTTTT | 7464 |
rs528739178 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98125071 | CAAACACCTTGTTTA[C/T]TTCACCCAATAAATG | 7464 |
rs528761782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170572 | TCAGCCTCCCAAGTA[C/G]CTGGGATTACAGGTG | 7464 |
rs528878418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125290 | AACTGCCCTCTGTGC[A/C]GAATGGGTGTTAGAT | 7464 |
rs528914317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149992 | GATGGAGTGCAGTGG[C/T]GCGATCTTGACTCAC | 7464 |
rs528982517 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192710 | CGGGGCGGGGGCCTG[A/G]CCCAAGGTCCGCCCT | 7464 |
rs529085795 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188632 | TAGCTGGTGTGGTGG[C/T]ACGCACCTGTAATCC | 7464 |
rs529092967 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168824 | GGCCAAGTGGCTCGT[A/G]AGAGTTCCAACCCCT | 7464 |
rs529132485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98161931 | CTCCTGAGAGCCACT[A/C]TCCATCCAGGAGGAG | 7464 |
rs529148088 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122203 | GGAGCTTGCTGTCCT[C/T]TTCATCTTTATTGCA | 7464 |
rs529163670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98129062 | CTTAGCGTCCCAAGT[A/G]GCTGGGACCACAGGT | 7464 |
rs529166372 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167231 | ACAGCGCATGATTCC[A/G]CTTATATGAGTTACT | 7464 |
rs529209428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180121 | CAGTGCTAAAACGCT[C/T]CTCCCTGACAGGGCA | 7464 |
rs529245318 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173590 | TGAGGCCAGCACTCC[A/G]GAACTGGGCGTCCCA | 7464 |
rs529253878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128410 | ACTTGCCCGAGGTCA[C/T]GCAGCAGCTCAAGAA | 7464 |
rs529330218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179024 | AGTGGTCACAGTCTA[A/G]CTCTTTACCGGTCCT | 7464 |
rs529377649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149083 | CAACAGTATGCTGTA[C/T]TGCGTACTGTAGTCT | 7464 |
rs529439176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98191469 | ATTTAAGGGACCTGA[C/T]CACTGCCCCAGGGTG | 7464 |
rs529442411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155374 | TTTTTTGAGATGGAG[C/T]CTGGCTCTGTCACCC | 7464 |
rs529591983 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120816 | CTTCCAGAACAGCCT[A/G]TGCTTTCCCTATCCT | 7464 |
rs529784106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182699 | CTCTCTGGGCTCCTG[A/C]CTCCTTATCTGTAAA | 7464 |
rs529819978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182172 | TGTGTCTGTTTTGCT[A/G]TGCTTGGTATCTCTA | 7464 |
rs529833105 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98152177 | TATTGCTCAATGTTT[A/T]GTAGTTAGAGGACTA | 7464 |
rs529944467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158929 | AGCCAGATCACAAGT[A/G]GCCTGTGAGAGGGTC | 7464 |
rs530030373 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98158189 | GGCAGCTCATGCCTG[A/T]AATCCCAGCATTTTG | 7464 |
rs530059419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98124969 | AGCTGAAAGCTAAAC[C/G]ACTATCCCTCTTTGA | 7464 |
rs530071602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163489 | GCCATTGTGCCCGGC[C/G]TTGAGTTTATTTCTT | 7464 |
rs530096554 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124217 | GATGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 7464 |
rs530101195 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98164190 | CCACAAGTTACCCAG[G/T]TATTTCAAAAACCGA | 7464 |
rs530120185 | in-del | -/AAAAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187296 | TCAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]TTAGCCAGGCATGAT | 7464 |
rs530158303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169802 | TCCCTCTGCCTAGAA[C/T]TAAGCCAGCTCAGGT | 7464 |
rs530300064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98136986 | AGCCACTGAACCTGG[C/T]ATATCTGTGGTTCTT | 7464 |
rs530393868 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178743 | TGAATTCTTTGTTCT[A/T]TTTGTTTAGATATTT | 7464 |
rs530406808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187554 | ACTAAGACAGCAGAT[C/T]TGGAGTCTGGTGAGG | 7464 |
rs530417691 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179124 | ATCTGTAAAATGGAA[C/T]GAATCAAACCAGCTC | 7464 |
rs530420557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161707 | GGCAGTGAAGTGGAC[A/G]GGATGGTGGGGAGAG | 7464 |
rs530455944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98138271 | AATACAAAAATTAGC[C/T]GGGCGTGGTAGCATG | 7464 |
rs530456753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168127 | AAGTTAAAATTAAAT[A/G]AAGTGTAAAATCCAG | 7464 |
rs530475445 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174013 | CCCAGCTACTCGGGA[A/G]GGAGAATTGCTTGAA | 7464 |
rs530511081 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120876 | AAAACTGGAGAGGGC[A/G]AAGACTGTCTGTTCT | 7464 |
rs530562977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161228 | TCAGATACCCGGACT[C/T]TGAGGGCAGTGGGGA | 7464 |
rs530633779 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98134365 | CCATCCCATCCACTC[C/G/T]GGGCAGGCTATAATG | 7464 |
rs530677063 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132314 | CTCCTGGAGGGACAC[A/G]TGCGGTCGGTATTGG | 7464 |
rs530685606 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172963 | TTACATGTGTTTGCC[C/T]GCTGTGTCACAGCAG | 7464 |
rs530748832 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155947 | ACTTTTGGCCCTTTT[A/G]TCTTCTCTAATGTAT | 7464 |
rs530775513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172504 | CACTTCCAAGCTCAG[C/T]CCCACACCCCACTTC | 7464 |
rs530775562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178830 | AAGATGAAGAGAGTC[A/G]GAGATAATTTTTAAG | 7464 |
rs530787560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133704 | CCATACAAACAGATG[A/C]GAAAGCGCTGTGGAT | 7464 |
rs530812893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178248 | GGCGGGGATTTGCTA[C/T]GTTGCCCAGGCTTGT | 7464 |
rs530875037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98140532 | TGTAGCCTCGAACTC[A/G]GGGTAAGACAATCTT | 7464 |
rs530905040 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98189881 | TCACTAGACGGCAAC[G/T]CCTTTATTTTTTTTT | 7464 |
rs530916578 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98160712 | CCTCACCTTGAGCAA[A/C]TGCTGGGGGTGGCGG | 7464 |
rs530941169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98190479 | AAAAAAAGGCACTCC[A/G]ATCTTGGAATCAGGA | 7464 |
rs530993117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147313 | TCCCTGGTTTTAGAA[C/T]TGCATACTGACATGT | 7464 |
rs530995135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98154007 | TGATTTATCTTTATA[C/G]ATTTACTAATATTAA | 7464 |
rs531031993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153286 | TTGTGTTTTTAGTAG[A/G]GACGGAGTTTCACCA | 7464 |
rs531128909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171737 | TGTGGTGTGCGGAGA[C/T]GGAGCCAGGAGCTTG | 7464 |
rs531191102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126326 | AGAGTGAGCCACTGT[A/G]CCCAGCCTCCCACCA | 7464 |
rs531211493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187569 | TTGGAGTCTGGTGAG[G/T]GCCCACTTCCTGGGT | 7464 |
rs531278785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132750 | CTCCTGACCCCCTGG[A/C]CAGAGCTGAGGCACG | 7464 |
rs531279112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125679 | ACCCACTAGGTCAAA[A/C]CCTCTCCATTTTACA | 7464 |
rs531334037 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193535 | CACGTCTGTGAAGAG[C/T]TCTTGGTTTTGTTCA | 7464 |
rs531523239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169094 | GAGCGCAGCCATCCA[A/G]GGACCCTCCTTTGGG | 7464 |
rs531561837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98168792 | CCAAACCAGAAAGCA[C/T]GAAGCAGCCTCCCAG | 7464 |
rs531627006 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123363 | CAAACTTCTAAAAAA[A/T]TTTTTTTTTCCTAGC | 7464 |
rs531657679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162168 | TGAACAGCAGGCCTG[C/G]GGGCTGCACTCAGCT | 7464 |
rs531667687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135722 | TAGTTGATTGTATGC[A/G]CTGTTTCCCTTAGAG | 7464 |
rs531728448 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | CORO2A | GRCh38.p7 | 9:98184492 | TCTCATTCCACACAT[-/A]ACTACTCTTTCTCTT | 7464 |
rs531755521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142613 | AATAGTCAGGCTGCC[C/T]TCGGGCTGACGGGAG | 7464 |
rs531768417 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98149656 | ACTCATTATCACAGG[A/G]AGGGCATCAAGCCAT | 7464 |
rs531813199 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144631 | AGAGACCTGGGGGAT[A/G]AACCAGAGAAGGCTC | 7464 |
rs531875989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135083 | CATAGCCACCTCCCA[C/T]TCAGTGGCTATGGGC | 7464 |
rs531897086 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194381 | TACTTGAATTACAGC[G/T]GGACGGTGGGCACCA | 7464 |
rs531906082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179586 | TCAAAGCCAAGGTGT[A/G]GCCCAGGAGTATATC | 7464 |
rs531941950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98185397 | TCCCCTTTTACAGAT[A/G]AGGACACTGAGTCAT | 7464 |
rs531950519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98192418 | GCAAGGTCACGCAAA[G/T]GGGCTGAAAGCCAGG | 7464 |
rs532032090 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120742 | CCCTGAGTATTCCAA[C/T]TTACTCTGCAGGTTT | 7464 |
rs532038016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191552 | AGGCAGTGACTGGGT[A/G]GCAGATTCCAGCTTG | 7464 |
rs532113401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139876 | CATTTCCCTCATTTT[C/T]CCCTTTCCTAATGAG | 7464 |
rs532147571 | snp | A/G | 3.31411e-05 | 0.00407056 | intron-variant | CORO2A | GRCh38.p7 | 9:98132323 | GGACACGTGCGGTCG[A/G]TATTGGAGAGACAGT | 7464 |
rs532152510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98139365 | TGGCATGGTGGCTCA[C/T]GGCTGTAATCCCAGC | 7464 |
rs532157370 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179905 | CTACTCAAGAGGCTG[A/G]GGCAGGAGAATTTCT | 7464 |
rs532183665 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98132877 | ATGGAAAGGACATAT[C/G]CCACCTTCCAGCAAT | 7464 |
rs532211021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177374 | CCTACTGGAGCAACG[C/T]TTGATCACAAACGTG | 7464 |
rs532212088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182994 | CAAAGAGGCTGAAAC[A/G]CCTGTGAGATGGGAT | 7464 |
rs532301298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183731 | TTGGGAGGCTGAGGC[A/G]GGCAGATTACTTGAG | 7464 |
rs532337680 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177113 | ACTCACACCTTTGAA[A/T]GGTGAACTGTGTTTC | 7464 |
rs532351013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189700 | AAGAGGAAGACTTCA[A/G]TCTGGAATCTATGTC | 7464 |
rs532437873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152386 | CCTTGAACTCCTGGG[C/T]TCAAGGCAGCCTCCT | 7464 |
rs532487202 | snp | A/C | | | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137650 | AACGTTGCCTCTGTG[A/C]CCGCAGACTTTTGGG | 7464 |
rs532562088 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98155535 | ATTTTTAGTAGAGAC[-/G]GGGGTTTCACCATGT | 7464 |
rs532585604 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124413 | TCTGGCCCAGTCTTC[C/T]CCTATTCTCTGGACC | 7464 |
rs532606215 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194144 | AATACAAAAATTAGC[C/G/T]GGGCGTGGTGGCATG | 7464 |
rs532651644 | snp | C/T | 2.17191e-05 | 0.00329531 | intron-variant | CORO2A | GRCh38.p7 | 9:98130933 | GGTCCAGGAGGTCAC[C/T]TCCCTCCCGTGCCAA | 7464 |
rs532672861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175219 | GGCCATCTCTGCCAG[A/G]GCCCCAGCAGAGGGG | 7464 |
rs532676729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164237 | ATCAGGATAAAGAAC[A/G]CTCTATGTGAAGGTG | 7464 |
rs532713014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98170503 | CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCACT | 7464 |
rs532753708 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98137848 | TGTGGGATCCTGGGG[G/T]AGTTACTTCACTTCT | 7464 |
rs532794402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169880 | TCACCCCACCTTCCT[A/G]GCCCAGCTCCAACAG | 7464 |
rs532795089 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143757 | TACTCACTGGGCAGG[C/G]GACAAACTGTTCTGC | 7464 |
rs532797049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138507 | TGCCCATCAAGTGAA[C/G]AATGGACATACAAAA | 7464 |
rs532803013 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174726 | CCCTGTGAAGAAGGT[A/G]CCAGCTTCCCCTTCA | 7464 |
rs532824851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182108 | TTCTGTGGGACTCTA[C/T]GATTACTGTCCATCT | 7464 |
rs532844905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191440 | CTGGGGCTGCTGGGT[A/C]TGGAGATGAGCATAT | 7464 |
rs532891889 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122031 | AAGCAGAATAAACCA[A/C]AGCTGGGTAAGGGGC | 7464 |
rs532942060 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98149296 | TTATCAGGCATCTCT[A/G]GGAGCTTGTTGGAGA | 7464 |
rs532970389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98191759 | CAGCACCTTGGCACT[A/G]TCACCCCTCTGAGGT | 7464 |
rs532987031 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172960 | CATTTACATGTGTTT[A/G]CCCGCTGTGTCACAG | 7464 |
rs533045048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126184 | GGGACTACAGGTGTA[C/T]GCCACCACACCCGGC | 7464 |
rs533087492 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129009 | ACAATCATAGCTCAC[C/T]GCAGTCTCACACTCC | 7464 |
rs533207877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98127602 | GGATCACTTGAGGTC[A/G]AGAGTTTGAGACCAG | 7464 |
rs533231561 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173056 | CACGCTTGTAACCCA[A/G]CACTTTAGGAGGCCG | 7464 |
rs533276584 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98190517 | GCTCGGTTGCTGGTT[C/T]GCTGTGTGACCTTTG | 7464 |
rs533298361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134483 | TTAGTTAAGATGAGA[A/T]CATAATGGATTAGGT | 7464 |
rs533321632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178936 | GACTTGTCCAGGGTC[A/G]CCTGGCTGGTCAGTG | 7464 |
rs533476734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147824 | ATTCACCCAAAAATA[C/T]GTACACAAATGTTTG | 7464 |
rs533572193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98154121 | TCTTCATGAGTGAGA[C/T]TGATCAATATTTTTT | 7464 |
rs533621338 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98130200 | ATCTTCCCGCCTCAG[A/C]CTCCCGAGTAGGTGG | 7464 |
rs533669179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181410 | GGAACTCCTGGCTTC[A/G]AGCAATCCTCATGTC | 7464 |
rs533747548 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98180810 | TAGAGGGCCCTGGAA[G/T]CCACAACCAGAGACC | 7464 |
rs533748132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169947 | AGCAGTCTCTCCATC[A/C]CATGAGGTCCCATCC | 7464 |
rs533753195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187107 | ACACTGTGAAACCCC[A/G]TCTCTACTGAAAACA | 7464 |
rs533764453 | snp | C/T | 0.000199198 | 0.00997794 | missense | CORO2A | GRCh38.p7 | 9:98130963 | AGCCGACCTTCCCCA[C/T]CACGTAGAGCATGCT | 7464 |
rs533833039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186535 | TATGTGGGATGAGAA[A/G]AGGAGAAGATATGGG | 7464 |
rs533863770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150182 | GTGATCTGCCTGCCT[C/T]GGCTTCCCAAAGTGC | 7464 |
rs533900396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156700 | AAGTCTGCTATTTGT[A/G]TTTCAGCTGACTCTC | 7464 |
rs533967392 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174150 | AAAACAAAAAAAAAA[-/AA]CCAAAGAGCGTGTAG | 7464 |
rs533971609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162298 | ACCTCTGTCCCTAAG[A/G]GGAACTGTCATGATC | 7464 |
rs533975446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144118 | CACTTGAGCCTGGGA[A/G]GTCCAGCCTACAGTG | 7464 |
rs534008349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162030 | AGTCATGGTTTTTGA[A/G]TGCTTACAAGCTGCC | 7464 |
rs534011067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98143092 | TGTGGTGTACAAGCT[C/G]TAAATCAGGGGAGAC | 7464 |
rs534071030 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164175 | TAGGGAAGATTAGAA[A/C]CACAAGTTACCCAGT | 7464 |
rs534080043 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122346 | GCATGGGCATCTGTA[G/T]TTCCTGCACGCTCCC | 7464 |
rs534092980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168385 | ACACATACTAGCTAA[C/T]GCCTATATTACTGAC | 7464 |
rs534096811 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133901 | TGGGACTACTTGACG[A/C]ATTTTCCCACACCTG | 7464 |
rs534130580 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138777 | GAACGGGCTGGGCGC[A/C/G]GTGGCTCACGACTGT | 7464 |
rs534135083 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173783 | AAGTCTTGATACCAC[A/C]TCGTCAGGTTGCTGT | 7464 |
rs534231137 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98142213 | CCTGCACCTGTGGCA[C/G]GCATTGCGAATGGAT | 7464 |
rs534352247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152959 | AACTGATGTAATTTG[A/C]ATTTGGGTTGTATAT | 7464 |
rs534363221 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175181 | CTCCCTGTCTGCTTC[C/G]CCTTTCACTCCTGGC | 7464 |
rs534401084 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158392 | CATGGCAGATACTTG[A/G]TCAACAGTGGCAATC | 7464 |
rs534453257 | in-del | -/TG | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98149049 | GTTCTGTATCTTGAC[-/TG]TAGTGATGCCAGTAT | 7464 |
rs534476646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127940 | GTAAAGAAGCTTTCC[G/T]TGGGGCAAAGTCCCT | 7464 |
rs534573599 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98132358 | GATCGGGGGCAGCTG[G/T]GGTTTCTGGCCTCCC | 7464 |
rs534588080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125345 | GTTATCCCACTGGAA[C/T]GTTGTGACACCCCTA | 7464 |
rs534588442 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125355 | TGGAACGTTGTGACA[C/T]CCCTATAAGGGTGGC | 7464 |
rs534598307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170874 | AGGACGGTCTGTGGA[C/G]GGTGCTGCAGCTTGC | 7464 |
rs534611214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132016 | ACAGGGTCTGGGCTC[A/G]CCCGGGGCTGTCAGC | 7464 |
rs534611250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139438 | TTTGAGACCAGCCTG[C/G]TCAATATGGTGAAAC | 7464 |
rs534696040 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183338 | CCACCTTCAGAAACC[C/T]CCACAGACATCTCCT | 7464 |
rs534712619 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123123 | ACCAGAGAGGGCAGG[A/G]CTTGCAAGAGGTCAC | 7464 |
rs534802948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126166 | TCAACCTCTCAAGTA[A/G]CTGGGACTACAGGTG | 7464 |
rs534828513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145001 | AGGGAGAGATGAGAG[A/G]AGCATTTCTTGACCC | 7464 |
rs534834646 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98156585 | TTAAGATTTATCTTT[C/T]GTTATTGATTTCTAA | 7464 |
rs534863809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171409 | GTTCAGCCAACATCA[C/T]TGGTGCCCACTCTGA | 7464 |
rs534899814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176973 | ACATTTTTGTTCCTT[A/G]TCTGTGTTGCTCTAA | 7464 |
rs535031148 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185648 | CAATTCCCCAGCCTG[A/G]GCCAACACCGTGGTG | 7464 |
rs535052194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98145761 | TCTGTCGCCCAGGCT[A/G]GAGTGCAATGGTGCG | 7464 |
rs535139309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151962 | GCTGGGACCACAGGC[A/G]CACGCCACCATGCCC | 7464 |
rs535160968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98187923 | ACACAGTTTCAATAA[A/G]CCATGTAACTTTTCT | 7464 |
rs535175677 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188042 | ACACAGTCTAGCCCA[A/G]GGCCTGCCTGCTCCT | 7464 |
rs535181672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159084 | ATTATTTTTGAGGAA[C/G]GATCTCGCTCTGTCA | 7464 |
rs535230351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98191847 | CACACACTAGCTCTG[A/G]GACACAGAGCTAGGC | 7464 |
rs535239109 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148509 | TTCCAGAAGTTTGGG[G/T]TGGGTGGATCACTTA | 7464 |
rs535265614 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167497 | ACAATGAAATATACA[C/T]ATATTTTTTAAAAGA | 7464 |
rs535276620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158413 | AGTGGCAATCACAGC[C/T]ACTAGTATCATCTGG | 7464 |
rs535358397 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121508 | TTAAATAATTTATTC[C/T]AGATGTAAAAATAAT | 7464 |
rs535411322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180662 | ATGCTCCACCTGCTT[C/T]CAAAGTCACTAATTC | 7464 |
rs535427626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98142744 | TAGACAGCTTCTCTT[C/T]CTTCTCAGCCTTCTC | 7464 |
rs535431083 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121558 | AAAGACACCTGTGTC[C/G]TGTTTGTTAAGTGTG | 7464 |
rs535439098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167786 | GACGGATGCCTAATA[G/T]TCACAGATGAAATGA | 7464 |
rs535454570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179840 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATT | 7464 |
rs535525628 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173205 | TTCTGATTCGGCAGC[A/G]TGGGTGAGAGCTGAG | 7464 |
rs535632981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148845 | CAATATATGCAACAA[C/G]CCAGCTGAACTGCGA | 7464 |
rs535637939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155837 | AGCTCTGCTGTGATA[C/T]TGTTTTTCTCATTCC | 7464 |
rs535644675 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98185102 | CTTCATAGTCTGGCC[A/G]TCTCCAAATCACACT | 7464 |
rs535658212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191254 | CCGGACCTCTCAGAC[A/G]GTCCCCAGGAGGGGC | 7464 |
rs535664196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184496 | CATTCCACACATACT[A/G]CTCTTTCTCTTACCG | 7464 |
rs535806939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160980 | CAGATGGTGCATCTA[C/T]AAGGTAGTTGGTCCC | 7464 |
rs535836158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127676 | AAAATTAGCTGGGCA[C/T]GGTGGCACGTGCCTG | 7464 |
rs535882922 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137485 | ATGGAGTCAGGGGCA[C/T]CAGAGCCAAGAACAG | 7464 |
rs535893259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170773 | GACACCAATTCGCTC[C/T]GTCACCTTGGGCAAA | 7464 |
rs535914498 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98163814 | CTGTTCCAAAGGCCC[C/T]TCTTCTTTACCCAGC | 7464 |
rs536012863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175338 | CCTGGCAGAGTCGTG[A/G]CTCTTCCCACCAACC | 7464 |
rs536044798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181860 | TCAAGAAAGGAACCC[A/G]CAACAAAGAAAACCA | 7464 |
rs536054571 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174870 | GTGAGAGTGGACTAA[C/T]ACAGATGGCTGCACA | 7464 |
rs536088612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140204 | AAGTGAAAGAGACAG[C/G]TGAGAAGAAAACTGG | 7464 |
rs536124788 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98137321 | TCACTGGGCTTTATT[A/G]GCTGGGTGGAACTAT | 7464 |
rs536146469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151393 | CAATGTTCTATCATT[G/T]TCCTTCTAAGCGTTG | 7464 |
rs536147378 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180393 | AGCATTCCCATCCAT[C/T]CCCTCGCAGGCCATG | 7464 |
rs536181770 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98190009 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 7464 |
rs536204727 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98164406 | TCTTTTCAGTCATCC[A/T]GAATCCTTATGGGGT | 7464 |
rs536213933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98158618 | CTGGGCCACTGGGAC[C/T]GACTGTACTATGGGT | 7464 |
rs536223868 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161919 | GGTCTGGCCCAACTC[C/G]TGAGAGCCACTCTCC | 7464 |
rs536276891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150273 | CTTCCCACTGGACTC[A/G]GGATAGAGCCCAGAC | 7464 |
rs536305434 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124690 | GAAATAGTGGTTGTC[C/T]TTGAGGGGACTTGTG | 7464 |
rs536392463 | snp | A/C | 0.000399281 | 0.0141238 | missense | CORO2A | GRCh38.p7 | 9:98131059 | GCACAGAGAGGTTAT[A/C]CTGCAGGGGAAGGGG | 7464 |
rs536405695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162366 | CCAGGAAGCTAGCTA[A/G]AACCCTCTGGAAAGG | 7464 |
rs536419750 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174848 | TCAGGTATGTCATTA[C/T]AGCAGTGTGAGAGTG | 7464 |
rs536427074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137956 | GAGGTATGGCACAGT[A/G]CCTAGCACATGGCAG | 7464 |
rs536520777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129527 | GACCTAGAACACATC[C/T]CTCTCTCCCCTGCTG | 7464 |
rs536530415 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180153 | GCTGCACCTACCTCC[C/T]TGCCCTTGGCGTCTG | 7464 |
rs536540980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187614 | TTCTTACTGTGTCCT[C/T]ATGTGGTGGAGGAGG | 7464 |
rs536583870 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194368 | ATGGTTTGGTTTTTA[A/C]TTGAATTACAGCTGG | 7464 |
rs536589160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128818 | CCTGAACAGAGACCA[A/G]TCTCCTCCCAGAAAA | 7464 |
rs536640317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148039 | ATCACTTGAGCTCAG[C/G]AGTTTGAGACCAGCC | 7464 |
rs536648484 | in-del | -/TTG | 0.00358779 | 0.0422022 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194430 | GGCATCTGAATAACT[-/TTG]TTGTTGTTGTTTTTG | 7464 |
rs536675063 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98154369 | CACAAATACATATAT[A/T]TATATATTTTAAATA | 7464 |
rs536770532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160899 | CCAGGCCAAAGCACA[C/T]GAGACCTGCCTGTGA | 7464 |
rs536772722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98162884 | AAGTGAGTACTGTAG[C/T]GGGCCCTTCGCCTAC | 7464 |
rs536799963 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123616 | TCTCCTATCTCAGCC[A/T]CCCGAATAGCAGGGA | 7464 |
rs536813211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169255 | TGCATCTCTGCAGGC[C/T]CACAGGAAGTACAGA | 7464 |
rs536864941 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148919 | TATTGTATGATTCCA[C/T]TTATGTAACATTCCT | 7464 |
rs536898207 | snp | G/T | 1.65723e-05 | 0.00287852 | missense | CORO2A | GRCh38.p7 | 9:98126562 | ACCTCATTCTCTGTC[G/T]TTGGTGGGGGGCATT | 7464 |
rs536988249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98126215 | TAATTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 7464 |
rs537009110 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190128 | GACCTCAGGTGATCC[A/G]CCCACCTTGGCCTCC | 7464 |
rs537028313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132445 | GCCTGGAGATTCTTC[C/T]CAGGGGCACCACCTG | 7464 |
rs537031721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140079 | CATCACATTGCATGG[C/G]CCTGGCAGAACAGGG | 7464 |
rs537058446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183833 | GGGTGTGGTAGTGCA[C/T]GCCTGTGATCCCAGC | 7464 |
rs537059614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190629 | TTCAGCTCAGACATT[A/C]CATGATTCCATGGTG | 7464 |
rs537182737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182488 | CCATTACTCAGAGTA[C/T]CAGGCTTTTAATGAC | 7464 |
rs537239948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145860 | TGGGACTACAGGCAT[A/G]TGCCACCACGCCCAG | 7464 |
rs537264355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188789 | AACAACAACAACAAC[A/G]AAAAACAACAACAAA | 7464 |
rs537279911 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98159811 | CTTCCTCAGAGAAGG[A/C]TCTGCTCCAGGAGTG | 7464 |
rs537301541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165625 | ACTGCTAACATGCAG[A/G]GCAGTGGCTTGCAAC | 7464 |
rs537415029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171505 | GGGAGCTCAGAGGAT[C/G]GGGGAGGCCCCCATG | 7464 |
rs537451938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177006 | AATAGTGGAAACTCG[C/T]TTGTGGAGGGACAAA | 7464 |
rs537467009 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121269 | CTCATCTCCTAGTGC[C/T]GTCCTCATTCTCAGA | 7464 |
rs537507938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135983 | TCCCCACTGCTAGAG[A/G]AGCAACCGTGCCCTC | 7464 |
rs537520613 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98139518 | TGTAATCCAAGCTAC[A/T]TGGGAGACTGAGGCA | 7464 |
rs537532789 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98180761 | TTGCCAGTGTCCCCA[A/G]TGATGGATCAGTAAA | 7464 |
rs537534064 | snp | G/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187234 | CTTGCAGTGAGCCGA[G/T]ATCGTGCTGCTGCAC | 7464 |
rs537541620 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153502 | ACCTCAAATTCGTGG[C/T]CTCAAGCAATTCTCC | 7464 |
rs537549388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98183169 | TCTTGCTCAGAAAGC[A/G]GCCCAAACTTCAGCA | 7464 |
rs537585542 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98189431 | TCTAAAACGATCCAG[C/G]TTCTGGCCATTTTGA | 7464 |
rs537633140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152579 | GTGAGCCACCCTGCC[C/T]GGCCTGTAGATGCTT | 7464 |
rs537668501 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192768 | CCACCCTTTTCCGCC[C/T]CCACGACCCCGACCG | 7464 |
rs537669852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151966 | GGACCACAGGCGCAC[A/G]CCACCATGCCCGGCT | 7464 |
rs537703644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192072 | GGCTTGGCGGGGACC[A/C]GGGGATGCCCCCCAC | 7464 |
rs537762728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98159162 | ACTCCTGACCTCAAG[A/G]ATCCTCCTGCCTCAG | 7464 |
rs537764870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156010 | TATTATCTCCTTCCT[A/C]AAACTTTCTTTGGGT | 7464 |
rs537807406 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174620 | TGGAGGCGGTTTCCC[C/T]CAGGCTGTTCTGGTA | 7464 |
rs537814001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161962 | TGAGGAGGCCGTGAG[A/G]GGCCTGGGCAACACC | 7464 |
rs537843130 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174161 | AAAAAACCAAAGAGC[A/G]TGTAGCCCTGGCCCA | 7464 |
rs537943291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98143008 | TGTCAGGGACATTTA[C/T]CATCAGGAGGCCATT | 7464 |
rs537961941 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98189151 | CATTTCTTGTAAGTC[-/AA]AAAAAGTCACATACT | 7464 |
rs538008671 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143071 | CAGAAACAGGCTTCT[A/G]ATGGATGTGGTGTAC | 7464 |
rs538026744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98150089 | GGTGGCTGCCACCAC[A/G]CCCAACTAATTTTTC | 7464 |
rs538030350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98134567 | CACAGAGAGAAGGCC[A/G]TGTGAAGACAGAAAC | 7464 |
rs538058457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179118 | TTCCTCATCTGTAAA[A/G]TGGAACGAATCAAAC | 7464 |
rs538063566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149456 | GAGGCTGAGTATTTA[C/T]AAAGAAAAGACGTTT | 7464 |
rs538286932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161477 | GAGAATCACTTGAAC[C/T]GGGAATGCGGAGGTT | 7464 |
rs538293375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128535 | CCAGGCTCTGGTGCC[C/T]GACAGCCCTGGGTCT | 7464 |
rs538294682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159285 | ACCTCCTGATCTCAA[C/G]CAATTCTCCTGTAGC | 7464 |
rs538309049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126007 | ACAGGTGTGAGCCAC[C/T]GCACCTGGTCACCTG | 7464 |
rs538322475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171232 | CTCAGAGAGGAAGCG[C/T]GCCTTGCTTAGCGTC | 7464 |
rs538353786 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139087 | ATGCAGAACGATACA[C/T]TCATGGAGACAGAAG | 7464 |
rs538385452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127745 | CTTGAACCTGGGGGT[A/G]GGGTGGAGGTTGCAG | 7464 |
rs538494332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133918 | TTTTCCCACACCTGG[C/T]TAATTTTTTCTATTT | 7464 |
rs538522157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131204 | TTTTATATGTGTGTG[C/T]GGGGGGAAGATGTCC | 7464 |
rs538544549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175422 | AGCACCAACTCCCAC[G/T]GGGCTTCAGCAGGGA | 7464 |
rs538558323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184523 | ACCGTGACATGGTGG[C/T]CCTCTCTCTAAACAG | 7464 |
rs538558852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138186 | TTGGGAGGCCAAGGT[A/G]GGTGGATCACCTGAG | 7464 |
rs538586907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181995 | TTCCTTTCCTTGACC[A/G]GCACCATCTGTGCCC | 7464 |
rs538621588 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130720 | CTGAGAAACACCAAT[A/G]GTCCCCCCACATCTG | 7464 |
rs538673959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151486 | TAAATATTCCCAGTA[C/T]GTACAAATGCAATTC | 7464 |
rs538792069 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150555 | CCTAAACTAGGTCCC[C/T]TCTCCCAACCCACGT | 7464 |
rs538804458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98131901 | GCCCTCTCCTTCTCC[C/T]TTCCTCCTAGTCCTG | 7464 |
rs538818019 | snp | A/G | 1.75151e-05 | 0.00295927 | intron-variant | CORO2A | GRCh38.p7 | 9:98157692 | GGACAAAGGGTATGA[A/G]GCTCACTGCCCTGAT | 7464 |
rs538822364 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98172237 | CACTTCTGAGCTCAG[A/C]CCCACGCCCTACTTC | 7464 |
rs538828865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176245 | ATTTAGAATCTAAAG[A/C]TCTAATTCTTCAGTT | 7464 |
rs538890547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138732 | GGTACCTGGTATCTG[C/G]AACCCTAAGTAATGC | 7464 |
rs538909395 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147324 | AGAATTGCATACTGA[C/T]ATGTGGTAGGGGGCG | 7464 |
rs538917805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182257 | TACATTGAAAGATAA[C/T]TTTTTAGGGAGCGAA | 7464 |
rs538964093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98188585 | GCCTGGCCAACATGG[C/T]GAAACACCGTCTCTA | 7464 |
rs539053621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187758 | GGGTAAGATTTCAAC[A/G]TATGAGCTTTGGAGG | 7464 |
rs539090906 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194428 | AAGGCATCTGAATAA[A/C]TTTGTTGTTGTTGTT | 7464 |
rs539096310 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2A | GRCh38.p7 | 9:98148726 | CACTGCATTCCAGCC[C/T]GGGTGAAAGAGCCAG | 7464 |
rs539147574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158273 | CAACACAGTGAGACC[C/T]TGTCTCTAAAAAAAA | 7464 |
rs539260245 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154107 | TAATTTGGCATCCAT[C/G]TTCATGAGTGAGATT | 7464 |
rs539314990 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98169381 | CCACCGTCCCTGGGC[A/G]GGCCACCTCCTCCTG | 7464 |
rs539382573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179424 | TGCTCCTATCTCTCA[C/T]CCTCCCCATCTTCCA | 7464 |
rs539415009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98172550 | GCCTCACTTCCAAGC[C/T]CAGCCCCACACCCCA | 7464 |
rs539539789 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148108 | AAAAGAAAAAAAAAA[-/AAA]GAGGCCAGGCAAGGT | 7464 |
rs539581555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190680 | TTAAAGTCATAGCAT[A/G]ACTTTTTAATAACCA | 7464 |
rs539682178 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98153381 | GCTGGGATTACAGGC[G/T]TAAGCCAGCGCATCC | 7464 |
rs539685008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160934 | CTAGGACTCTCGTCC[C/T]TGGCCAAAGGGATGA | 7464 |
rs539714598 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150135 | ACAGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 7464 |
rs539721750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166643 | AATAGAACGATCATA[C/T]GATTCAGCAACTCCA | 7464 |
rs539859683 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167773 | TTTATCTTTTAGAGA[C/T]GGATGCCTAATATTC | 7464 |
rs539916354 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98177845 | ATACACAGAGTGAGA[A/T]TCATCACTAACCAGA | 7464 |
rs539965235 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98166347 | AACAGGCAACAAAAG[-/A]AAAAAAAATAGACAA | 7464 |
rs540022887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168583 | GGTCCACACTCTCTC[A/G]CAGGGGTTCCTGGAC | 7464 |
rs540036348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139579 | TTGCGGTGAGCTGAG[A/C]TTGTGCCACTGCGTT | 7464 |
rs540036713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147423 | TGAAGCAAGAGGGCA[A/G]ACTTGATAATTCTAG | 7464 |
rs540075878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98146710 | AGTGAGAGCAAGGCC[C/T]GAGGCCACACCCAGG | 7464 |
rs540171851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185675 | GGTGCAGCCTTAGGA[A/T]CAGCCACAGGAGTTG | 7464 |
rs540191078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98157211 | GGAGGAAATAAATTC[A/G]CAGAATTATATTGCA | 7464 |
rs540254423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98185230 | CTCCTGGGCTTCCCT[A/G]TGATAACTGTAGTGC | 7464 |
rs540274835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98162648 | GTGCTGGCCTGTGTG[C/T]GTACTGTGTGTGCAC | 7464 |
rs540294688 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176834 | AAATGGAGTCAGCAC[A/G]CCAAAGGCCACCCAC | 7464 |
rs540305884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168931 | ATCCAAGAGAGTGCA[C/T]TTGTGCATCTCTCCG | 7464 |
rs540313229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162125 | TCAGATGTAGGTGTT[C/T]AGGCCAGTAACCGGG | 7464 |
rs540331218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191438 | GCCTGGGGCTGCTGG[C/G]TCTGGAGATGAGCAT | 7464 |
rs540334660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129707 | TGTCTCCCCAGACCC[C/T]GCACTGAAGCCCTGA | 7464 |
rs540375542 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160674 | CAAATCAGCAGGCTC[C/T]GCTCCAGGCCCCCCC | 7464 |
rs540393667 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174237 | GCATTTGAGTAGCTT[C/T]CCTAAACCTCTCTGT | 7464 |
rs540394927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161509 | CAGCGAGCCAAGATC[A/G]CACCACTGCACTCCA | 7464 |
rs540466070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135619 | GAGTAAGCTCCCTGT[C/T]ACAGAGGTATACAAA | 7464 |
rs540470560 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140858 | TGATCAGACACCTCC[A/G]CCTAGACTGGATCCC | 7464 |
rs540473445 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190770 | GGGCCCAGATTATAC[A/G]TGTGTCGAGATGACA | 7464 |
rs540509044 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142624 | TGCCCTCGGGCTGAC[G/T]GGAGGCAAAGTGCCC | 7464 |
rs540553358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179395 | GGGTCTCATGAAGCA[A/G]TGACCTGCAATCCTG | 7464 |
rs540556462 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161287 | AGCTGGGCACGGTGG[C/T]TCACACCTGTAATCC | 7464 |
rs540600031 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172884 | AGCAAAGATGTCAGT[A/G]CCCCTGTGGGAAAGG | 7464 |
rs540644275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192203 | GGGGCCTGTCGGGAC[C/T]GGCTGGCCGCGCCCA | 7464 |
rs540700812 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131143 | TAAGAATTGCTGCCA[C/T]GGTGCTCTGGGCGAG | 7464 |
rs540784987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159457 | ATTCCATATTCCAAG[A/G]TTCTTTTCTTCTAGC | 7464 |
rs540802589 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121799 | ACTGAGTGGAGGTGG[C/G]AGGAATTTGTAAACT | 7464 |
rs540825184 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131538 | AGCTCAGGCTGGTCT[C/T]GAATTCGTGGCCTCA | 7464 |
rs540871037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98164541 | ACAGCATCTTCCTTT[C/T]TCACCAGGCAGGAAG | 7464 |
rs540872897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158906 | ATACAAGCCAGAGGG[A/G]CGAGGAGAGCCAGAT | 7464 |
rs540981072 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172927 | CAAGACTGGCTGTGA[C/G]GACAGGTGACAGCAT | 7464 |
rs540986557 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121491 | CCTTGCTGTGAAATA[A/G]TTTAAATAATTTATT | 7464 |
rs541020455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139041 | ACAGAGCAAGATTCT[A/G]TCTCAAAAAAAAAAA | 7464 |
rs541060065 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155505 | GTGCCCGCCACTGTG[C/T]CTGGCTAATTTTTGT | 7464 |
rs541060907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138286 | CGGGCGTGGTAGCAT[A/G]CACCTGTAATCCCAG | 7464 |
rs541062896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130773 | AGGTCAAGGTGTCCA[A/G]CCAGAGCCCTGGCTC | 7464 |
rs541064488 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124153 | CAAGTCGCTGGAATT[A/G]CAGGCGCCTGCCACC | 7464 |
rs541078547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189065 | CCAATCTCTCAATTA[C/T]AGTAAGGAGCACACC | 7464 |
rs541198822 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134400 | AACAGGGTTCCCCCC[-/A]AAAACTCATGTCCAC | 7464 |
rs541253963 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190740 | AAAGGCTTGAATTAG[G/T]CAAGCAGGAAAACAG | 7464 |
rs541402540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128113 | CAATTGCTTGGGGCC[A/G]CTGGGCACGCCATGT | 7464 |
rs541423239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175629 | GGCTCTGAGGAAGAA[C/T]GGATGCAGAGGGGCT | 7464 |
rs541434191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98168012 | GCAGGAGAGCACAGA[A/G]GTGGCCCAGGCCCCG | 7464 |
rs541492106 | snp | A/G | 0.000274748 | 0.0117174 | intron-variant | CORO2A | GRCh38.p7 | 9:98134763 | TATTCCAGTTTGTGG[A/G]AACTTGTTGGGGCTG | 7464 |
rs541593937 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149044 | GGAATGTTCTGTATC[G/T]TGACTGTAGTGATGC | 7464 |
rs541715568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190776 | AGATTATACATGTGT[C/T]GAGATGACAGGAGAC | 7464 |
rs541858062 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173484 | CACGGGCTCCATGAG[C/T]ACTCAACCACCCCCC | 7464 |
rs541940747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166146 | CATGTTAACAGCCAC[A/G]CAGATACAATCAGGA | 7464 |
rs541944309 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98179260 | GACCGCTAGAGCATG[A/G]GGATTCTGCCTCTGC | 7464 |
rs541982806 | snp | C/G | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98178810 | TTTGGAGGCAATTGG[C/G]ATAGAAGATGAAGAG | 7464 |
rs542028272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172050 | GGGCTGGAGGGGTTG[C/T]GGAACCCCATGAGGA | 7464 |
rs542039484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140486 | CACTCTGTTGTCCAG[A/G]CTGGAGTGCAGTGGT | 7464 |
rs542087621 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179144 | CAAACCAGCTCTTGG[A/G]CTGCTGTTTGAGTGC | 7464 |
rs542148764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183486 | CCTGCAGCCTGCTGA[C/T]GTCAGACCGGCCTGA | 7464 |
rs542153888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190268 | GTCCCCAAAGTAGCC[A/G]GCTAAGGGCAAAGGG | 7464 |
rs542197866 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194014 | TATGGATGGCTGGGC[A/G]CAGTGGCTCATGCTT | 7464 |
rs542311827 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172279 | CCACACCCCACTTCT[A/G]AGCTCGACCCCACGC | 7464 |
rs542327758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160240 | AAGGATTTAAGAAGA[C/T]TCACAAAAATAGAAC | 7464 |
rs542476909 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98132701 | AAGCGCTTGCCCAAG[G/T]CTGCACAGTGGCTAA | 7464 |
rs542510247 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174317 | ATAGAGGAGATGTTC[A/C]TTCATATAAAGTGCC | 7464 |
rs542684041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98157843 | CAGTTACTTCTGTAG[A/T]CCTGGTAAGATAAGA | 7464 |
rs542685549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98142571 | CAATTTCCGCAGTGC[A/G]GTTTCCCAAGAAAAG | 7464 |
rs542729495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149596 | GTGTGCCGCAGGCCA[C/T]GGGGAGGTGTCCCAG | 7464 |
rs542766271 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98156255 | ATGTTGCCCAGGCTG[G/T]TCTCAAACTCTTGGG | 7464 |
rs542784175 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123940 | GATTATAGGCGTGAA[A/C]CACCACGCCCTGCCT | 7464 |
rs542818958 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123355 | CTAGCTTTCAAACTT[C/T]TAAAAAAATTTTTTT | 7464 |
rs542886211 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159058 | CCACCTCATATCACC[C/T]TTTATTTATTATTAT | 7464 |
rs542898918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98161608 | AGATAGAGGACCAGA[C/T]TTAATTTTCAGGTTT | 7464 |
rs542913704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136346 | TTACGTTCCTCAGCA[C/T]CTGCTATATGGAAAC | 7464 |
rs542922930 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135968 | TGAAGCAGAGAAGAC[G/T]CCCCACTGCTAGAGG | 7464 |
rs542972526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171230 | GGCTCAGAGAGGAAG[A/C]GCGCCTTGCTTAGCG | 7464 |
rs542989887 | in-del | -/ATTTT | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98152284 | TTTATCTTATTCCTG[-/ATTTT]ATTTTATTTTATTTA | 7464 |
rs543001708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98143151 | AACCCTGGCTTGGGC[C/T]GCCCTGCCTGGAGAG | 7464 |
rs543027878 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98177258 | CTCCACCCACATTTT[A/C]CAAGTCCCCAGCTGG | 7464 |
rs543037361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135662 | TGATCCTGGGATGCT[A/G]CTGACTTGATCTTCC | 7464 |
rs543039212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98140273 | CAGGGGACAGGTGCT[A/G]TTGGAGGGGCTGATT | 7464 |
rs543042144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147552 | TTGAAAATGCAATTG[A/G]CAAACAAGTAGATCG | 7464 |
rs543060417 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152428 | CTGAGTAGCTGGGAC[C/T]ACAGGCATGCTCCAC | 7464 |
rs543067776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184051 | ATGACTTAAAGTATA[C/T]AGGAGGGTGTGTGTA | 7464 |
rs543126239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146939 | GTGCTATGGCATGGT[A/G]CCTGCACAGTAGTAA | 7464 |
rs543158641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98149087 | AGTATGCTGTACTGC[A/G]TACTGTAGTCTTATA | 7464 |
rs543164358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146250 | GTGACTCTGTGGCAG[A/G]CTGGGCCCCAGGCTC | 7464 |
rs543164370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153064 | ACAGACCGAAGTACA[A/G]TATTTGGGGGTAAAG | 7464 |
rs543184950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191502 | GGAGGAAGGGTCAGA[A/G]GTTGTTTGTGTGTCC | 7464 |
rs543231523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189144 | AAATTGCCATTTCTT[A/G]TAAGTCAAAAAAAGT | 7464 |
rs543252243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162070 | TCCAAATGCTTTCCA[C/T]GCATGAATAGAGCAA | 7464 |
rs543300883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98160033 | TAAGGGCCTGACCCC[C/T]GAGGCAAGCCCTTTA | 7464 |
rs543547233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189662 | GAGAGGGGAACGGAT[C/T]GGCCCAAGGTCACAC | 7464 |
rs543557811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138831 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 7464 |
rs543711337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181690 | TTTGGCAAGGCTGTT[C/T]CTCCTATGCAGCGTG | 7464 |
rs543749386 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194628 | ATAGGGTTTCGCCAC[A/G]TTGCTCAGGCTGGTC | 7464 |
rs543802094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187557 | AAGACAGCAGATTTG[C/G]AGTCTGGTGAGGGCC | 7464 |
rs543848911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171026 | CCCCAAATCAAGCCC[A/T]GACCAAAACTCCACA | 7464 |
rs543870150 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121983 | ATGGAGAATAAGACA[A/G]GGAACACGAGCATCC | 7464 |
rs543924068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170273 | TTCTGCTGTGCCCAC[C/G]TACAGCCCTGTGGGT | 7464 |
rs543961131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175797 | CTCTCTTGGCCTTGG[A/G]TTTTCTCATCCATAA | 7464 |
rs543983953 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98138491 | GTGGAAACAACCCAA[A/C]TGCCCATCAAGTGAA | 7464 |
rs543989715 | in-del | -/ATGTACCA | 0.102726 | 0.202016 | intron-variant | CORO2A | GRCh38.p7 | 9:98165111 | TAGCTAAGAACAAGC[-/ATGTACCA]ATGTACCACCGTGCT | 7464 |
rs544002894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98139571 | GGTGGAGGTTGCGGT[A/G]AGCTGAGATTGTGCC | 7464 |
rs544011419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182094 | TCTCCTCCTCCAGAT[C/T]CTGTGGGACTCTACG | 7464 |
rs544058729 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98133946 | TTTTTTTGTAGAGAT[-/G]GGGTCTCACTATGTT | 7464 |
rs544067311 | snp | A/G | 6.65879e-05 | 0.00576971 | missense | CORO2A | GRCh38.p7 | 9:98134877 | CCAGGCCTACTCTGC[A/G]CGCGTGGCCCACGAG | 7464 |
rs544075147 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166034 | CTGCTAACATGAAGC[A/G]ACAGGAAACACTACT | 7464 |
rs544089195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179312 | CTGCAGGACGCGGAG[A/G]CCCTGCTGCCCAGCA | 7464 |
rs544143440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98151667 | AACTTTTCTTTCGCT[A/G]TTTTTCTTTTTTTGA | 7464 |
rs544228976 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98168516 | ACTTGCCTAAGATCA[A/C]ATAGCTAGTTAGTGG | 7464 |
rs544242005 | in-del | -/GCT | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98151010 | TGTTCTGGCCAGACA[-/GCT]GCTCTCTGCATTGCT | 7464 |
rs544261580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128914 | GACTCTTCACCTTCA[A/C]AGATTTAAATTATTT | 7464 |
rs544285125 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162465 | GTCCCCCAATCCTCT[-/C]CCCACCCTAACTCTT | 7464 |
rs544296390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135566 | GACTTCCTTCCAGAG[C/T]AGTGTTGTCTGAAGA | 7464 |
rs544312863 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173912 | ACCTGAGATCGGGAG[C/T]TCGAGACTAGCCTGA | 7464 |
rs544350022 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173544 | TGGCTTGCTTTCTTA[A/T]GTCTCTTCTCAACAT | 7464 |
rs544361769 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98141070 | TACCCTCAAAGAGTT[-/C]TGAAAACAAAAAATT | 7464 |
rs544362860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98166974 | CTGGGCATGGTGGCA[C/T]ACACCTGTAGTCCCA | 7464 |
rs544370067 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143109 | AAATCAGGGGAGACA[C/T]GCCTGCTCCCCTCGC | 7464 |
rs544517573 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98141174 | GTTAGTGATGTGCAT[G/T]GAGGGAGGTGAAAAT | 7464 |
rs544530952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178067 | AAACATTTTTTTAGA[A/G]ACAGAGTCTCGCTCT | 7464 |
rs544580235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133330 | GGGAGGGTGGCGCAG[A/C]TGGCAGCCTGGCCAA | 7464 |
rs544639493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98152032 | ATGTTGGCCAGGCTG[C/T]TCTCAAACTCCTGAC | 7464 |
rs544652096 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131798 | CCCTCACCCTACCCT[A/G]CTCCACCCTCAGCTG | 7464 |
rs544659734 | snp | G/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194076 | GTGGATTGCTTGAGC[G/T]CAAGAGTTCAAGACC | 7464 |
rs544754716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98160725 | AACTGCTGGGGGTGG[C/T]GGGAGTGCACCTGTC | 7464 |
rs544790863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166309 | CATTGGGCTTGGCAA[C/T]GATTCCTTGGTTATG | 7464 |
rs544800272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98127332 | GTACACCAGGAGGCC[C/T]GCTCAGCCACTGGGG | 7464 |
rs544804728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170068 | AGTATCCTCATATTT[C/T]TCTCATAGAATCTAG | 7464 |
rs544806892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98163210 | TTTTTTTCTTTGAGA[C/T]GGAGTCTCGCTCTGT | 7464 |
rs544847318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98157950 | AAGGCAGAAGAACCA[C/T]AGAGAGAATCCACCA | 7464 |
rs544879614 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147870 | TAATAGCCCCAAACT[C/T]GAAACAACCCACTGG | 7464 |
rs544888496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126841 | GGAAGGGAAGCAGAG[C/G]CATGTGAGGACGGGG | 7464 |
rs544892190 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174348 | TCAGAGCAGTGCTTG[A/G]CAAGTGCTCAGCCAG | 7464 |
rs544894228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169631 | TCCCCCTGAGTCTTT[A/G]ACCTCCTTCTCATCT | 7464 |
rs544961118 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158797 | GGGGGAACCACATGT[C/G]GTTTAGTAAGATTAT | 7464 |
rs544962405 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155804 | CAGTTGCTTGTATTA[C/G]TTCTTATTAGATTTC | 7464 |
rs544999718 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135388 | GCTGCATCCTCAGGC[A/C]CTAGGGAGCCGGCGA | 7464 |
rs545036505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144408 | AGGATTGGGAATGTT[G/T]CCTCTTATGGCCTGG | 7464 |
rs545066660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158770 | AGGTGTCTTAGGCAG[A/G]TAGAACAGTTTGGGG | 7464 |
rs545069359 | snp | A/G | 8.23716e-05 | 0.00641709 | missense | CORO2A | GRCh38.p7 | 9:98129821 | GTGGGTTATAGGAGC[A/G]GTACTCAGTCAGGTA | 7464 |
rs545081005 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98131551 | CTCGAATTCGTGGCC[A/T]CAAGTGATCCTCCCG | 7464 |
rs545108580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98136611 | TTGGAAAGAGAATGG[A/G]CTGTGGAATCAGACA | 7464 |
rs545111594 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98190043 | GCATGTGCCACCACA[-/C]CCAGCTAATTTTTAT | 7464 |
rs545120115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98143514 | GTGGAATCCCTGCCA[C/T]ATCCCTTACCATGGT | 7464 |
rs545160602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150437 | CACTCAGGGGAATGT[C/T]TGCATGTTCTATTTG | 7464 |
rs545184060 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173057 | ACGCTTGTAACCCAG[C/T]ACTTTAGGAGGCCGA | 7464 |
rs545202461 | snp | A/G | 0.000121139 | 0.00778169 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124846 | CTGGACCTCTCGCTG[A/G]GTCAACAGCTCCCGG | 7464 |
rs545294275 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124106 | GCAACCCCCGCCTTC[C/T]GGTTTCAAGCAATTC | 7464 |
rs545297223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130532 | ACTGGGGTGGCCTCA[A/G]AGGTCATCCAGAAGG | 7464 |
rs545316285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98174937 | AAAAATGGTTAAAAT[C/T]GTAAACTTTGCTATG | 7464 |
rs545355328 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186777 | GTGGTAAGAAGTGCT[A/G]ATAAGTGTTTGTTAA | 7464 |
rs545362773 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98156333 | GTGTGAGCCACTGTA[A/C]CCGGCTCTAACTTCT | 7464 |
rs545383041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137488 | GAGTCAGGGGCACCA[A/G]AGCCAAGAACAGGTA | 7464 |
rs545442324 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188278 | AACTGCCCCCTCACA[C/T]ACCCTAACCCCTCCT | 7464 |
rs545479182 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170863 | GCCCACCTGTTAGGA[C/T]GGTCTGTGGAGGGTG | 7464 |
rs545513121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140430 | CCCATCTGTGTAGAG[A/G]CCACTGTACTTGTTT | 7464 |
rs545551749 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98147659 | ACAACAAATATTTTA[A/G]CATAAGGAGGTTCCA | 7464 |
rs545558141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186775 | TGGTGGTAAGAAGTG[C/T]TAATAAGTGTTTGTT | 7464 |
rs545593276 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193238 | GCCAGCCTCGCTGGC[C/T]GGAGAGCCCTGAGGA | 7464 |
rs545627729 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124018 | CTGGTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 7464 |
rs545639584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147035 | ACTTTGGGGGGCTGA[A/G]GCAGGAGGATCCCTT | 7464 |
rs545659207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98162464 | CGTCCCCCAATCCTC[C/T]CCCCACCCTAACTCT | 7464 |
rs545757692 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98160607 | GGTCTTGGCAACTTG[A/G]TGGCAGTGGAGGAGC | 7464 |
rs545791896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98172208 | CCCCACTTCTGAGCT[C/T]GGCACCCCCACCCCA | 7464 |
rs545867637 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150964 | GTCCACTTCCTTAGG[A/G]TACTTCCCTTCTTCT | 7464 |
rs545952413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126270 | TGAACTCCTGACCTC[A/G]TGATCTGCCCGCCTT | 7464 |
rs545956200 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98184238 | TTTTATTTTATTTTT[A/T]TTTTTAATAGAGGCA | 7464 |
rs546011165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177074 | TGAGCTCAAGGGTCA[C/T]TGGCCTTATCTAGGC | 7464 |
rs546035971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188402 | TGATTGTAAGCTCTT[C/T]GGGGGAAGATCTTTC | 7464 |
rs546061350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153172 | TGGCACGATCTCAGC[C/T]CATTGCAACCCCTGC | 7464 |
rs546080384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189713 | CAATCTGGAATCTAT[C/G]TCTGCTGACTTTAGT | 7464 |
rs546122939 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98183998 | ATAACTAGTTACATA[G/T]CATTTACATTGTGTT | 7464 |
rs546127338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98188877 | TGGCTGAATGACTAA[G/T]GGAATGAATGAACAT | 7464 |
rs546130834 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147481 | TTATTTTTATCTACT[A/T]TTGTGCTTGAGATTT | 7464 |
rs546142041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142245 | CCAGCACCCTCTCTC[C/G]GACCTCAGACTTGGG | 7464 |
rs546145219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160203 | GGATGGACTGACTAA[C/T]TAATGCCCATGTGAT | 7464 |
rs546223073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165263 | CGTGCCTGGCTTACA[C/T]GTAACAATTCTATTG | 7464 |
rs546358510 | snp | A/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98155810 | CTTGTATTAGTTCTT[A/T]TTAGATTTCAAAGCT | 7464 |
rs546382443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181455 | TGCTAGGATTATAGG[C/T]GTGAGCCTCGGTGCC | 7464 |
rs546394039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176623 | GGGTTTCTTGTGTGA[C/G]TTGGTTTCCCATGTC | 7464 |
rs546445801 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182935 | ACAGATAAGCCCTGC[C/T]TTGAATGAAATACCG | 7464 |
rs546461363 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165317 | TGTCAAGTTGTCTGC[A/G]AGAGAGGAGGCTCTA | 7464 |
rs546511963 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121318 | AAAGGGGACGCCCAG[A/G]GTATGGAATAAGGAG | 7464 |
rs546530681 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98149921 | GTAGGACAAGTGAGT[C/T]TCTTTTTCTCTTTCT | 7464 |
rs546541994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145942 | GTCTCGAATGCCTGA[A/C]CTCAAGTGATCTCCT | 7464 |
rs546544225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138538 | TGCAGTATATTCATG[C/T]AGCAGAATACTACTG | 7464 |
rs546618505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98156524 | TTTTGTTTATGGCCT[A/G]TAAATTATTTAGAAA | 7464 |
rs546741753 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179552 | TTCCAAAACCTTCAA[C/T]AGCTTCTCAGCTGGG | 7464 |
rs546770445 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137374 | GAACTAAGGCCCATA[A/G]AGAGGAGGGGTGGTG | 7464 |
rs546773072 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122106 | AGAGATGTTGAGGGA[C/G]GGCTTGGGGCAACAC | 7464 |
rs546827321 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191988 | CACCTCCAACCTAGG[A/G]CTCCTCCAGCCCCAG | 7464 |
rs546850795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98180370 | CTCTTCCAGGAAGTC[C/T]TCCTGCAAGCATTCC | 7464 |
rs546919242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166329 | CCTTGGTTATGATAC[C/T]AGGAACAGGCAACAA | 7464 |
rs546939716 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125315 | TTAGATATTGAGTGA[A/T]GCCCTAAGGGCCTCG | 7464 |
rs546948482 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162427 | GACAGCAAAAGAGCG[G/T]GAACATCAGTGCCCT | 7464 |
rs546961101 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174490 | GTGAAATCAAAATGT[-/A]AAAATCTTGGCAGTG | 7464 |
rs546999333 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156958 | TTGATCTATGTGAAA[A/G]TGTTGCTTTTTTGGG | 7464 |
rs547013147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176130 | ATCTAAACATTCGGC[A/G]GGGGGTGAGGGGTGT | 7464 |
rs547029294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178350 | AACCTCTTCCATTCC[C/G]TTGTCTTCATGTACT | 7464 |
rs547046652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182126 | TTACTGTCCATCTCT[C/T]GTTTGGTCTGTGAGC | 7464 |
rs547063192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133830 | ATGATCATGGCTCAC[C/T]GTAGCATCAACCTCC | 7464 |
rs547064549 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130526 | GTCAGAACTGGGGTG[C/G]CCTCAGAGGTCATCC | 7464 |
rs547099489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140695 | AACAATCTTCCCAAC[C/T]TGCCCTCCTAAAGTT | 7464 |
rs547264082 | in-del | -/TCTGCCTCCCGGGT | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98151900 | CGACTCACTGCAAGC[-/TCTGCCTCCCGGGT]TCACGCCATTCTCCT | 7464 |
rs547304745 | snp | A/C | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123361 | TTCAAACTTCTAAAA[A/C]AATTTTTTTTTCCTA | 7464 |
rs547355307 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98150758 | AATCTTTTACAAGCA[G/T]GCAAAGCTTGGAAGA | 7464 |
rs547406523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131674 | TTCCCCTACCTGTTT[C/T]TTAAAATTTATTTTA | 7464 |
rs547443254 | snp | A/G | 0.000250568 | 0.0111902 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98130967 | GACCTTCCCCACCAC[A/G]TAGAGCATGCTGGTG | 7464 |
rs547532987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137918 | CAGGTATTTCACAGG[C/T]TGGTGTGAGGATCAT | 7464 |
rs547543807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98136956 | GTCTCCCAAAGTGCT[A/G]AGATTACAGGTGTGA | 7464 |
rs547554664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187575 | TCTGGTGAGGGCCCA[C/T]TTCCTGGGTCATAGA | 7464 |
rs547576637 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187383 | AGAATCACTTGAACC[C/T]GGGAGACGGTGGCTG | 7464 |
rs547576993 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122952 | TGTTGTAGAATTGGG[C/T]TGAATGCCTCTGACC | 7464 |
rs547610663 | snp | G/T | 0.030278 | 0.119257 | intron-variant | CORO2A | GRCh38.p7 | 9:98168829 | AGTGGCTCGTGAGAG[G/T]TCCAACCCCTGGTGC | 7464 |
rs547611403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151379 | TATTAGTCTTTTAAC[A/G]ATGTTCTATCATTTT | 7464 |
rs547612213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135860 | AGGCTCCAGATACTT[C/T]GGTCTGATGAGGGCT | 7464 |
rs547665870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129470 | GAGGCTCTTCTAGGT[C/G]AGCCCTTTCCATCTC | 7464 |
rs547697100 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174142 | CAAAACAAAAAACAA[A/C]AAAAAAAAACCAAAG | 7464 |
rs547701839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142660 | CCCCATTCAGACACA[C/T]ACCTCCCACCTCCCA | 7464 |
rs547709525 | snp | G/T | 3.29794e-05 | 0.00406061 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133194 | GATGACAGACTCCTT[G/T]GTATCCAGGTTCCAG | 7464 |
rs547756599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161210 | GGCAGGACCCAGATC[A/G]TCTCAGATACCCGGA | 7464 |
rs547794357 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98160866 | GTGGATCATGGGAGG[A/C]AGTGATGTGTGTCAC | 7464 |
rs547862752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98148472 | CATAATTGAGGCCAG[A/G]TGCAGTGGCTCATAC | 7464 |
rs547871952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167627 | ATCCTGTGTGGATCC[A/G]GATTCACACAAACCA | 7464 |
rs547881628 | snp | A/T | 4.2252e-05 | 0.00459611 | intron-variant | CORO2A | GRCh38.p7 | 9:98126939 | ATGCAGACCCATGCA[A/T]CATGTGTGGGAAATA | 7464 |
rs547979884 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98166538 | CAAACAATTTGATTT[G/T]AAACAATCTGATTTA | 7464 |
rs548011900 | snp | C/T | 0.00013485 | 0.00821018 | intron-variant | CORO2A | GRCh38.p7 | 9:98132995 | GTCCCCACTCTGCTC[C/T]TTGCTCCTCTGAGCC | 7464 |
rs548014627 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98172410 | CTTCTGAGCTCGACC[C/T]CACGCCCCACTTCCG | 7464 |
rs548025604 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147365 | GTTGAAATGACAAAA[G/T]GTCTAGGATTTGCTT | 7464 |
rs548028767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181222 | GAGAAGGGCACTGCC[A/G]GAAAAGCCAGAACCC | 7464 |
rs548075786 | in-del | -/AAAAAAAAAAAAAA | 0.49889 | 0.0235361 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187283 | GCAAGACTCCATCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAATT | 7464 |
rs548153231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186153 | AAATGCTCAGCTCCC[A/G]ATTTCTTATTTGAAT | 7464 |
rs548205745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140023 | ACACCAGTTCAGTCA[C/T]AGAACCTTGGACTGG | 7464 |
rs548243976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147225 | ACCAGGGACCATTAA[C/T]ATGAATTAGGAATCA | 7464 |
rs548403239 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160131 | TCTCCTTTCGGGAGC[C/T]TTGCCCTAAACCCTG | 7464 |
rs548428170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178230 | TATTAAACTTTTCCT[C/T]GAGGCGGGGATTTGC | 7464 |
rs548464808 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98177676 | GTTTCACCATGTTGG[C/T]CTGGCTGGTCTCGAA | 7464 |
rs548467438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181741 | TGCTCAGTCCCTACT[C/T]ATCTTTCAGATCTCA | 7464 |
rs548508814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165069 | AACCTCCTGGGCTTG[C/T]GCAATCCTCTGGCTT | 7464 |
rs548561073 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98143232 | AGGACAGAAGGACCC[-/AGG]AGGAGTCAGGCGGGT | 7464 |
rs548565301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125509 | CCTCTGTGTTCTTAG[A/C]CACTACAGACTGACT | 7464 |
rs548602952 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98146491 | CTCTGAGAAGGACTT[C/G]CTGCACGCTGTGGCA | 7464 |
rs548629659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98189370 | TCTGCTGAATTATTT[C/T]CTGGACCTCCTGAGA | 7464 |
rs548644197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153213 | CAAGTGATTCTCCTG[C/T]CTCAGACTCCTGAGT | 7464 |
rs548679124 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98152525 | CTGGGCTCAAGAGAT[C/T]CACCCATCTTGGCCT | 7464 |
rs548702101 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170170 | AAGCGCCCCTCGTCT[C/T]CTTTCCTGCCCACTG | 7464 |
rs548742978 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98142846 | CCTCCCCTGCCCTGC[C/G]CTGCCCTGCGCTGCC | 7464 |
rs548771792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186289 | TGGCTGGCGGGGGGA[A/G]GGGCTAGGTTTGGGG | 7464 |
rs548772045 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98159793 | TTCTCTGCTGGCTTG[C/G]AGCTTCCTCAGAGAA | 7464 |
rs548944645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187051 | TTGGGAGGCTGAGGG[C/G]GGCAGATCATGAGGT | 7464 |
rs548980866 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173599 | CACTCCGGAACTGGG[C/T]GTCCCAATCCTCCTC | 7464 |
rs549012634 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122237 | AGGTACACATGCAGT[A/C]TTCCATCTTCACTGT | 7464 |
rs549037642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150569 | CCTCTCCCAACCCAC[A/G]TCACACTCTATCACA | 7464 |
rs549172404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98162148 | TAACCGGGTCACACA[A/G]CTAGTGAACAGCAGG | 7464 |
rs549185488 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168002 | CAAGAAAGAAGCAGG[A/C]GAGCACAGAGGTGGC | 7464 |
rs549261401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141420 | GCAGCGGTGCGATCC[C/T]GGATCACTGCAACCT | 7464 |
rs549290293 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98184777 | TGTGTGGTTAATGGC[A/G]GCTGTCTGTCTCTGT | 7464 |
rs549324437 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151181 | TATGCACCCAACTAC[A/G]TTAGGAGGTACTAGC | 7464 |
rs549351595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98148515 | AAGTTTGGGGTGGGT[A/G]GATCACTTAAGCCCA | 7464 |
rs549378115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191024 | ATACCTGTGATGACA[A/G]AGAGCTCACTACCTG | 7464 |
rs549415983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176800 | CAGACCCCAAGAGAT[C/T]GTGGGGTACAGAAAG | 7464 |
rs549417820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170792 | ACCTTGGGCAAATCT[C/T]GTCCCCTCTCCCGCT | 7464 |
rs549424522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98135008 | GGGCACCTTGGCACC[A/G]TCACCAGCCTAAGCC | 7464 |
rs549428653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127709 | GTCCCAGCTACTCAG[A/G]AGGCTGAGGCATGAG | 7464 |
rs549512892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98134551 | ATAAGGAAGACAGGT[A/G]CACAGAGAGAAGGCC | 7464 |
rs549557587 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123169 | ACAGCTGAGGCCAGA[A/G]GCAACAGATTTCTAC | 7464 |
rs549613961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145525 | GAAGGGCAATTTGTA[A/T]GGAGGGAACAGATAT | 7464 |
rs549624961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139357 | ATTAGGCCTGGCATG[A/G]TGGCTCACGGCTGTA | 7464 |
rs549627941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148003 | TGTAATCCTGGCACT[C/T]TGGGAGGCTGAGGCA | 7464 |
rs549653503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182848 | TTTAACATCTCTGAA[A/C]CTGGGATGCAACTTA | 7464 |
rs549656773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98190600 | GTTGAATGAGACGAC[A/G]TCTGAAGGCTCCTTT | 7464 |
rs549681723 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168757 | GGGAGGCCAGCATTT[C/T]GGGTATCTAAGTAAA | 7464 |
rs549793921 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98125849 | CAGCCTCCAGAGTAG[A/C]TGGGACTACAGGCAC | 7464 |
rs549868368 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124306 | GGCGTGAGCCACTGC[G/T]CCTGGTGAGACTGGT | 7464 |
rs549918543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131840 | GCTCCTTCTCCCCAT[A/G]CCCGTTAGTACCTCA | 7464 |
rs549953893 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123639 | AGCAGGGACTACAGA[C/T]GCTCACCACCACGGC | 7464 |
rs549955792 | snp | C/T | 0.000497353 | 0.0157616 | intron-variant | CORO2A | GRCh38.p7 | 9:98130906 | CAGGCTGCTGTCTGC[C/T]GCTGTCTCAGGGGTC | 7464 |
rs550013162 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188555 | GGATCATTTGAGGTC[A/C]GGAGTTCGAGTCCAG | 7464 |
rs550153489 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147701 | ACTTACACTAAAAAT[C/T]TGTAAAAATAAATTG | 7464 |
rs550238006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163546 | CCTGCAAGGTAGGTG[A/G]GGATTATTTTCCCCC | 7464 |
rs550270099 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120930 | GACTCCAAGAGTAGA[G/T]AGTTAATTGGTATTT | 7464 |
rs550316108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155165 | GTAGTTTTTCAAATG[C/T]TTATTAGCCATTTGG | 7464 |
rs550358091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98127570 | TAATCCCAGCACTTC[A/G]GGAGGCCGAGGCAGG | 7464 |
rs550394038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161294 | CACGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 7464 |
rs550405387 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176967 | TACCAAACATTTTTG[C/T]TCCTTATCTGTGTTG | 7464 |
rs550523581 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155577 | GTCTCGAACTCCTGA[A/C]CTCATGATCCACCCA | 7464 |
rs550533648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181295 | ATCCATCACTAATCC[C/T]AGCCTCCTGTCCCAC | 7464 |
rs550571540 | in-del | -/T | 0.125874 | 0.217008 | intron-variant | CORO2A | GRCh38.p7 | 9:98164976 | TAGGTGTAACAATTC[-/T]TTTTTTTTTTGAGAT | 7464 |
rs550622998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98133711 | AACAGATGAGAAAGC[A/G]CTGTGGATCGGAAGA | 7464 |
rs550624314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190480 | AAAAAAGGCACTCCA[A/G]TCTTGGAATCAGGAT | 7464 |
rs550627782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181552 | TCCGAAATATGTAAA[C/T]GTGAGCAGACCCCTC | 7464 |
rs550628124 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161620 | AGATTTAATTTTCAG[A/G]TTTTCCTCTGATTCC | 7464 |
rs550637289 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167247 | CTTATATGAGTTACT[C/T]TGAGTAGGCAAAATC | 7464 |
rs550643472 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178255 | ATTTGCTATGTTGCC[C/G/T]AGGCTTGTATCAAAC | 7464 |
rs550657744 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133315 | AAACACAGTATCCCT[G/T]GGAGGGTGGCGCAGC | 7464 |
rs550659868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140584 | CCAGGCTAAGAACTA[C/T]AGGCATGTGTCACCA | 7464 |
rs550676151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184369 | GTAGAAAAGACCAAA[G/T]AAAACAAAATTCTAC | 7464 |
rs550811577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98166605 | CTATGAAAGATAGTA[C/T]GGCAGTTCATCAAAA | 7464 |
rs550883789 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177411 | TGTTAGAGGTAGCAG[G/T]AGCAAGGAAAAGACC | 7464 |
rs550981725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98165366 | GCCCAACATACCGAA[C/T]CATAGAATAGAAATT | 7464 |
rs551027050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187570 | TGGAGTCTGGTGAGG[C/G]CCCACTTCCTGGGTC | 7464 |
rs551068100 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192342 | CCCGCGAGAAGGGGG[C/T]CACCAATGAGCAAGC | 7464 |
rs551082633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147339 | CATGTGGTAGGGGGC[A/G]GGGGGCAGAGGTTGA | 7464 |
rs551134760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98137194 | AGCCTTTTATAGCTC[A/G]CTTCCTCACTATGGG | 7464 |
rs551147446 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193552 | CTTGGTTTTGTTCAG[C/T]AGAGACGGGTTATCT | 7464 |
rs551173217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151284 | TCCTAAAAAAAGAGA[A/G]TGCTGTGGGAATTTG | 7464 |
rs551207787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98152634 | TATTTGCACTATTTA[A/G]CAAATAAGTCAAGTT | 7464 |
rs551245229 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98153364 | TCTGGGCCTGCCAAG[G/T]TGCTGGGATTACAGG | 7464 |
rs551254438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162731 | TGCATGCACGTGTGC[A/C]TCCCTTTGGATGTTT | 7464 |
rs551300048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126330 | TGAGCCACTGTGCCC[A/G]GCCTCCCACCATCTT | 7464 |
rs551331120 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126454 | CAGCTGGTTATTCTT[C/T]TCATGCCTCATTTTC | 7464 |
rs551377196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168802 | AAGCATGAAGCAGCC[C/T]CCCAGGGGCCAAGTG | 7464 |
rs551417918 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174055 | GAGGTTGCTGTGAGC[C/T]GAGATTGCGCCATTG | 7464 |
rs551444932 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98144807 | AGGCTGGAGGACAGG[G/T]CAAGAGAGGAGGCTG | 7464 |
rs551500386 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173677 | GCGTCTGCTGTCCCA[C/T]AACAGCTTCGCAGCC | 7464 |
rs551520959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142615 | TAGTCAGGCTGCCCT[C/T]GGGCTGACGGGAGGC | 7464 |
rs551562035 | snp | C/T | 8.23879e-05 | 0.00641772 | missense | CORO2A | GRCh38.p7 | 9:98157563 | TTGTCGTGAACGCTG[C/T]GGGTGATAGGCACGG | 7464 |
rs551572811 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150659 | TGCAAGTTAGAAACA[A/C/G]TGACAGTTCTGAGAG | 7464 |
rs551600609 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154558 | AGTCGTAACCCTCTC[C/T]ATCCCCCAGGGGTAA | 7464 |
rs551643937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135175 | CTCCAGCCTGAGCAG[C/G]GGCCAGCGCTGACCA | 7464 |
rs551725150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98160363 | GTTAAGCTAGGTGTG[C/T]GGCCAGGTCCACCAC | 7464 |
rs551752498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185442 | ACTTGCCTAAGGAGC[A/G]TATCAGCAGCGGGGT | 7464 |
rs551846852 | in-del | -/A | 0.476184 | 0.178115 | intron-variant | CORO2A | GRCh38.p7 | 9:98166944 | ATCTCTGCTAGAAAT[-/A]AAAAAAAAAATTAGC | 7464 |
rs551879359 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128873 | TGGGCTGGGCCCTAT[G/T]TTGGGAAATGGAGTT | 7464 |
rs551910704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139911 | CCTGTATAGGTGCTG[C/G]GAGGGACATACAGGT | 7464 |
rs551933956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98144279 | GCTGCGTTGCTCATA[A/G]TATTTGATTTACCTC | 7464 |
rs551981335 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98171763 | GCTTGCAGCGCGGGG[G/T]TGGGGAGGCTGGGTC | 7464 |
rs551988165 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183974 | TTAAAAATATGTATA[G/T]ACAGTATAATAACTA | 7464 |
rs552005722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132895 | ACCTTCCAGCAATCC[C/T]GAGAGGACAGACAGG | 7464 |
rs552037426 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98146430 | GACCCTGCCTGCAGT[C/G]TCACTCCCTTTGGGA | 7464 |
rs552053315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98184900 | AATCACAATGAATAA[C/T]GAATAGGTAGGTGCC | 7464 |
rs552112737 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121327 | GCCCAGGGTATGGAA[G/T]AAGGAGATGAGAGCA | 7464 |
rs552259342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152454 | TCCACTATGCCTGGT[C/T]AATTTTTGCATTTTT | 7464 |
rs552272615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126072 | ATGGAGTCTTGCTCT[A/G]TTGCCCAGGCTGGAG | 7464 |
rs552282821 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98171325 | CAGGGGTCCTGCATT[C/T]TGTTCTCAGCGTGGA | 7464 |
rs552341066 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179249 | CTGAGATCTGGGACC[G/T]CTAGAGCATGAGGAT | 7464 |
rs552369192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176921 | CGCTAAAACACAGAA[C/T]AGAGTCCTGTCTTCC | 7464 |
rs552424077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98183777 | CCAGCCTGGCCAACA[C/T]AGCGAAACCCCATCT | 7464 |
rs552490419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125008 | GGTGGAGGCGGTCAC[A/G]TTAACATGGCTGAGG | 7464 |
rs552507323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134652 | GGAGAGGCATGGAAG[G/T]ATTCTTCCCTAGGGC | 7464 |
rs552542866 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CORO2A | GRCh38.p7 | 9:98184871 | ATATTTCCCTAACCC[C/G]TAGGGGCTCCAGAAA | 7464 |
rs552543784 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162971 | CCTGCCCCATTCCAT[C/G]TGGCTGGGCCCACAT | 7464 |
rs552547910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176066 | ATTAAACTAGAAGCA[C/T]AAAGTGTTCATGGTC | 7464 |
rs552549344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151952 | CTCCCATGTAGCTGG[A/G]ACCACAGGCGCACGC | 7464 |
rs552591948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188594 | ACATGGCGAAACACC[A/G]TCTCTACTGAAAATA | 7464 |
rs552634027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159030 | TGAATACCAAGCCCT[C/T]ACCACCCCACCCCCA | 7464 |
rs552673629 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98134597 | CAGAGCCTGGAGTGA[C/T]GCAGCTATAGCCAAG | 7464 |
rs552692589 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155671 | TTTTAAAGTACATAA[A/T]GGACTATTCCTTTAA | 7464 |
rs552815031 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160373 | GTGTGCGGCCAGGTC[C/G]ACCACACAGAGGAGG | 7464 |
rs552858138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148163 | TCTTTGGGAGGCTGA[A/G]GCAGGCAGATTAACT | 7464 |
rs552858503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98169921 | AAGGAGCCTCCCCAG[C/T]TCTCAGACTGAGCAG | 7464 |
rs552861558 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154990 | GTCACAGGTATATGC[A/G]TTTTCTTCTTCTTTC | 7464 |
rs552875217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175232 | AGGGCCCCAGCAGAG[A/G]GGCTCGGTAGGGTGG | 7464 |
rs552888486 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98190753 | AGGCAAGCAGGAAAA[A/C]AGGGCCCAGATTATA | 7464 |
rs552894942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98154699 | GTTAATTAAATGATA[C/T]AGTTTAAAATTTGTT | 7464 |
rs552930562 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175237 | CCCAGCAGAGGGGCT[C/T]GGTAGGGTGGGGAGG | 7464 |
rs552989540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179224 | GCTCTGGAAGGTCCT[A/C]CTTGAGTGTCTGAGA | 7464 |
rs553041139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191163 | TGCTCCCTCAAACAG[C/G]GCAGGCATCAGGGAG | 7464 |
rs553075153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184978 | GAGCCTTACAACAAG[A/C]TTATACATTAGGCAG | 7464 |
rs553112046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98184583 | CTCCCGTCCTCTATC[C/T]CTATCCCTGGCAGGT | 7464 |
rs553148796 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183465 | GCTGTGAGTGCTGAC[C/T]TCATCCCTGCAGCCT | 7464 |
rs553221254 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98189928 | CTCGCTCTGTCGCCC[A/C]GGCTGGAGTGCAGTG | 7464 |
rs553292144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127280 | AAAACTAGGACTCGG[C/T]CCTGGTCCGCTGCCC | 7464 |
rs553300139 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98160954 | CAAAGGGATGAGAAG[C/G]GTGCATGTTTCAGAT | 7464 |
rs553336805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166676 | TCTGGAATATACACC[C/T]TTAAAGAAATGAAAG | 7464 |
rs553462354 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188073 | CTCTTCCTCTTCTCC[C/T]GCCATCACTCTGTCC | 7464 |
rs553477657 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124642 | GGAATCTCTTTCAGC[A/G]ATGGAGAGTTTTGTT | 7464 |
rs553486324 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98132478 | TCCCTCTCATCCACA[G/T]GGAGTCTCTCCCCAC | 7464 |
rs553510465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169978 | TGACATTTGGGGAGG[C/T]AGCCAAAGGCAGGGA | 7464 |
rs553519230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177085 | GTCATTGGCCTTATC[C/T]AGGCTCTCCTGGACT | 7464 |
rs553558912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140167 | CACCCACCAGAATGC[G/T]CCCCCAGCCATTTTT | 7464 |
rs553609527 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177688 | TGGCCTGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7464 |
rs553643895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98139592 | AGATTGTGCCACTGC[A/G]TTCCAGCCTGGGCAA | 7464 |
rs553659296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186577 | GTCTGTTTTCCTGCC[C/T]TTTTCTGAAATTCTC | 7464 |
rs553682968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146773 | CACAGGGTCCTCTGG[A/G]AAGTCATCTTCCTGA | 7464 |
rs553726369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144258 | TATGTGCCAGGCCCA[C/G]TGCCAGCTGCGTTGC | 7464 |
rs553755686 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123843 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 7464 |
rs553839229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98156212 | GCCCAGTTAATTTTT[A/G]TATTTTTTGTACAGA | 7464 |
rs553880604 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174785 | GGCTCCCCAGCCATG[C/T]GGAACTGTGAGTCAA | 7464 |
rs553881617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98149571 | ATGCAGACAGTGAAG[G/T]GGGGATCAGGTGTGC | 7464 |
rs553884188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162043 | GAGTGCTTACAAGCT[C/G]CCAGGCGCCATTCCA | 7464 |
rs553907175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192226 | CGCGCCCAGAGTGAG[C/T]TTCCCTCACCGCGGG | 7464 |
rs553917847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130220 | CGAGTAGGTGGGACC[A/T]CAGGTGTGTGCCACC | 7464 |
rs554052706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136329 | TCGGCAGACACTGTC[C/T]TTTACGTTCCTCAGC | 7464 |
rs554099624 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121817 | GAATTTGTAAACTGT[A/G]AAGTGCTAGCCACAC | 7464 |
rs554183526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128047 | GGACTGAAGGTCAAG[A/G]GCATGGCTTCTGAGG | 7464 |
rs554231284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153036 | TAAGAGAATATTCTC[A/G]TTCTTAGAAGATACA | 7464 |
rs554261286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190020 | CTCCCGAGTAGCTGG[A/G]ATTACAGGCATGTGC | 7464 |
rs554333836 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122350 | GGGCATCTGTATTTC[C/T]TGCACGCTCCCAAGG | 7464 |
rs554370823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128776 | GGGGCCACAGTGTTA[G/T]GGCCAAAGCCAGGCT | 7464 |
rs554384299 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98125200 | TGTTTTCGCCACCAC[C/T]GAACTGTGTGACCTT | 7464 |
rs554402836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98153730 | CAAAATGTTAAAACC[A/G]GTAAACCAGGTGAAG | 7464 |
rs554407559 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173786 | TCTTGATACCACATC[A/G]TCAGGTTGCTGTGAG | 7464 |
rs554455879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132392 | TTTGCTTATGCCACC[A/G]CTCCACCTGGGAGGC | 7464 |
rs554460441 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98182661 | CCTCTTGCTGGCTGC[A/G]TGACCTTGCAAATTT | 7464 |
rs554492013 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98165202 | GGCCTCAGGCGATCC[A/T]CACACCTCAGCCTCT | 7464 |
rs554554885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179771 | GCACTTTGGGAGGTC[A/G]AGGCAGGTAGATCAC | 7464 |
rs554580873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189657 | GTCCAGAGAGGGGAA[C/T]GGATCGGCCCAAGGT | 7464 |
rs554724243 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178701 | CAGCTGGCGAGTGTG[C/T]CTCCACCTGGCAAAT | 7464 |
rs554799867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164702 | CCGGCCAGCAACAAG[G/T]TCTGAAGTGATACAG | 7464 |
rs554824108 | in-del | -/AC/ACACAC | 0.160303 | 0.233355 | intron-variant | CORO2A | GRCh38.p7 | 9:98158840 | AAAAGAAGAAAACAC[-/AC/ACACAC]ACACACACACACACA | 7464 |
rs554867250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125360 | CGTTGTGACACCCCT[A/G]TAAGGGTGGCAGTGC | 7464 |
rs554868125 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160640 | CCTTGGGCCTGGGCT[C/T]GGGTGGGAAAGCAAG | 7464 |
rs554887877 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CORO2A | GRCh38.p7 | 9:98170918 | ACACAGGACCACAAG[A/G]GCGACAGAGCTGTCC | 7464 |
rs554896033 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180398 | TCCCATCCATCCCCT[A/C]GCAGGCCATGGCTCC | 7464 |
rs554897163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128882 | CCCTATGTTGGGAAA[C/T]GGAGTTGAATTAATC | 7464 |
rs554957230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185672 | CGTGGTGCAGCCTTA[A/G]GAACAGCCACAGGAG | 7464 |
rs555067055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182406 | TGAGGCTAGTGACCC[C/T]GCCAGCAAGCTCTCA | 7464 |
rs555105714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182045 | GTGACCCCGGACTCA[A/G]CACATTCTCTACTCT | 7464 |
rs555107560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98145054 | ATGCACAGCACATTC[C/T]CATGATTTAGGGCAG | 7464 |
rs555122217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98156761 | TTGTGGATTCATATT[C/T]CTCTATGTTTAATCT | 7464 |
rs555148089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98151637 | TATTTCTTCCTTTTC[C/T]ATCCTAACACTTTCA | 7464 |
rs555176686 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194550 | CCCACCTCAGCCTCC[C/T]GAATGGCTAGAACTA | 7464 |
rs555243960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141825 | TGCAGGATTGTTGAG[A/C]GTTAAATGAGATACT | 7464 |
rs555298559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191284 | CAGGAAGCTGGGGAG[A/C]CACATTCCAGTCCTG | 7464 |
rs555381333 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98135526 | GGCCTGTATTTCATG[C/G]TGAGGGCCTGAGAAG | 7464 |
rs555413185 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190505 | CAGGATCCCTGGGCT[C/T]GGTTGCTGGTTTGCT | 7464 |
rs555481362 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172628 | CGCTACTCTCTCACC[G/T]GCTTGTTAACATGGA | 7464 |
rs555490879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160986 | GTGCATCTATAAGGT[A/C]GTTGGTCCCTCAGGA | 7464 |
rs555506732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179305 | AGTGACCCTGCAGGA[C/T]GCGGAGACCCTGCTG | 7464 |
rs555509015 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123582 | TCATAGCAACCTCCA[A/C]CTCCCAGGTTCAAGC | 7464 |
rs555518112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178437 | ATCTTTAAAAACCAC[A/G]TGTCCATTCTGTAAG | 7464 |
rs555529410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166765 | TTAAATGTGGAATCA[A/C]CCCAAGTGTCCGTTC | 7464 |
rs555565138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149447 | GGAATATGTGAGGCT[A/G]AGTATTTACAAAGAA | 7464 |
rs555660143 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186032 | GCCCAGGGAACACAC[A/G]CCTGCCCCTGCACTG | 7464 |
rs555738202 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194663 | ACTCCTGGGCTCAAG[A/C]AATCTGCCTGCCTTG | 7464 |
rs555745290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167867 | AGGAGGGAATGAGTG[C/T]GTAGAGATGAAACAG | 7464 |
rs555762170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140221 | GAGAAGAAAACTGGC[C/T]AACATCCATCCATCC | 7464 |
rs555835258 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189537 | TCTCCTTCCAATCTC[A/G]GCTTTGCTACTGAGA | 7464 |
rs555883084 | snp | C/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98170042 | TATTTGTCTCTGTGC[C/T]GTAGCATTAGAGTAT | 7464 |
rs555900704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164414 | GTCATCCAGAATCCT[C/T]ATGGGGTCTCTGATC | 7464 |
rs555918075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169523 | ATTCCACCCCCAACT[C/G]TGGCCCTGCACTTTC | 7464 |
rs555921718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175393 | CCCCTTGAGGGACCA[C/G]GGACCCCCTAATTAG | 7464 |
rs555991156 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187857 | ACCCAATTCAAAAGC[C/T]TTCCATGGCTCCCCG | 7464 |
rs556003783 | in-del | -/C | 0.00318978 | 0.0398085 | utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98192663 | GAGCCGCCGCCGCCT[-/C]CCCCTGCAGCCCGGC | 7464 |
rs556100274 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169701 | CTCCCCTCAAAGCAT[C/T]GTGCTTTTCAAAAGA | 7464 |
rs556117440 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181030 | TCCCTCACGCCACTG[A/G]CTTTTTTTTCACATC | 7464 |
rs556147730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181890 | ATACAAGGAGAGTCA[C/T]TTCCAAGCTGTGTGA | 7464 |
rs556150467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98150961 | CCAGTCCACTTCCTT[A/C]GGGTACTTCCCTTCT | 7464 |
rs556242363 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164436 | TCTCTGATCCACCCA[C/T]TGCGAGTGGGATATC | 7464 |
rs556309483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186708 | TAATAACAAACAGTA[G/T]GTACCCTATAGGTTG | 7464 |
rs556353294 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124095 | CTCAGCTCACTGCAA[C/G]CCCCGCCTTCCGGTT | 7464 |
rs556456346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98129568 | CCTCTTTCAGTTCCT[C/T]CAATGTTGCCTCCTC | 7464 |
rs556498723 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166580 | GTAGGAATGCAAAAG[A/G]GTTTAGTTGCTATGA | 7464 |
rs556509155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187237 | GCAGTGAGCCGAGAT[C/T]GTGCTGCTGCACTCC | 7464 |
rs556548262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148119 | AAAAAAAGAGGCCAG[A/G]CAAGGTGGTTCATGT | 7464 |
rs556622258 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193721 | CACTATTATTACCTC[A/C]ATTTTACAGATAAGA | 7464 |
rs556622792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168495 | AGGGCACAGAGAGGT[C/T]ATATAACTTGCCTAA | 7464 |
rs556671864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153607 | AGAGATGGGGTCTTG[C/T]TATACTGCCCAGGCT | 7464 |
rs556709921 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193129 | CAGCGGTTACCGAGG[C/T]TTCCCCGTCCGCAGG | 7464 |
rs556768787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168857 | TGCAAACCATGATGA[G/T]GGGGAAACAGACACA | 7464 |
rs556860417 | snp | C/T | 0.00130336 | 0.0254947 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126786 | TGGGTGGGGTCTCAG[C/T]AGCTCAGAGCCAGGC | 7464 |
rs556894740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126235 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCATGCTG | 7464 |
rs556922243 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98140330 | TGACTTTGCAGAATC[A/C]ATAGTCTTGGGATTT | 7464 |
rs556934599 | snp | A/G | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174149 | AAAAACAAAAAAAAA[A/G]AACCAAAGAGCGTGT | 7464 |
rs556989264 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160549 | GAAATGGGTACTGGG[A/G]GTCCCCTTGGAAAGA | 7464 |
rs556991853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184235 | TTATTTTATTTTATT[A/T]TTTTTTTTAATAGAG | 7464 |
rs557066868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190630 | TCAGCTCAGACATTC[C/T]ATGATTCCATGGTGC | 7464 |
rs557123732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189457 | TTTGAAATAGCAAAG[G/T]TTTAAGGCTGAAACC | 7464 |
rs557124942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98132460 | CCAGGGGCACCACCT[A/G]GATCCCTCTCATCCA | 7464 |
rs557174641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160072 | CAGGTAGCACGTCAG[A/T]CTTGCAGGGGCTTGT | 7464 |
rs557246934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98165808 | AGTCCCCCATTAACC[A/G]TATCACTAGGGAACT | 7464 |
rs557293498 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123093 | GGTACCCCTGGTTCA[G/T]ATGAAGAAACTGAGA | 7464 |
rs557296204 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158940 | AAGTGGCCTGTGAGA[A/G]GGTCTAGGCCTCTTT | 7464 |
rs557298315 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178324 | AGTACTGGGATTACA[C/G]GCCAGCACTCAACCT | 7464 |
rs557307153 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98189536 | ATCTCCTTCCAATCT[C/T]GGCTTTGCTACTGAG | 7464 |
rs557396893 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98159207 | AGGACTACAGGTACA[A/T]GCCACCATACCTGGC | 7464 |
rs557413739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98132078 | CACCTGGCAGTCTAC[A/G]CTAAATGTGTGTGTC | 7464 |
rs557431262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130171 | AGCTCATTGCAACCT[C/G]CTGGTCTCAAGCCAT | 7464 |
rs557439020 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172520 | CCCACACCCCACTTC[C/T]GAGATCGACCCCATG | 7464 |
rs557458832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177032 | ACAAATTCCAAAGAT[A/G]GTTAGGAAAGAAAGG | 7464 |
rs557514887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186513 | GAAAGTAAATGTTCA[C/T]ATTGATTATGTGGGA | 7464 |
rs557521744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182503 | CCAGGCTTTTAATGA[C/T]CAGGCCACTGGAGCA | 7464 |
rs557566317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155226 | GTTTTGTGGATTTTT[C/T]GGTACATTTTATACA | 7464 |
rs557600711 | in-del | -/AGTT | 0.00438332 | 0.0466095 | intron-variant | CORO2A | GRCh38.p7 | 9:98136776 | GATAAGTGTGATGAC[-/AGTT]AGGAATACAGTGGGC | 7464 |
rs557612776 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173915 | TGAGATCGGGAGTTC[C/G]AGACTAGCCTGACCA | 7464 |
rs557685198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151978 | CACGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 7464 |
rs557728921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191398 | TTGCCTTGGCTCCCT[G/T]GGATCTGATGGGAGA | 7464 |
rs557782754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129670 | GTTGCTATGCTGTCT[C/T]TCCTCCCATCTGACT | 7464 |
rs557806085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168877 | AAACAGACACACACA[A/T]GCAGAAGGCTAGCTG | 7464 |
rs557817166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136005 | CGTGCCCTCCAGGCC[C/T]TGAAGGCAGGGAGGA | 7464 |
rs557880526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180775 | AATGATGGATCAGTA[A/C]AAACAGGTTCAGGCT | 7464 |
rs557897658 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150485 | CCCTTTAGAGCCTCA[A/G]GTGGCTCTCGGCTCA | 7464 |
rs557953254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98143031 | AGGCCATTTCCACCT[G/T]CTGCCCATTAGGCCA | 7464 |
rs557992183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150124 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 7464 |
rs558015671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98141514 | CGTGCCACCACACCC[A/G]GCTAGTTTTTGTATT | 7464 |
rs558065548 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98156015 | TCTCCTTCCTCAAAC[A/T]TTCTTTGGGTTTATT | 7464 |
rs558136370 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98159922 | AAGATAAAGAAGATG[C/T]TCACCCAGCCCACAC | 7464 |
rs558251676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98151685 | TTTCTTTTTTTGAGA[C/T]GGAATTTTGCTCTGT | 7464 |
rs558326429 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182119 | TCTACGATTACTGTC[C/T]ATCTCTCGTTTGGTC | 7464 |
rs558345413 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120722 | TTCTTCCCAAATGCC[C/T]TTTGCCCTGAGTATT | 7464 |
rs558348897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98170839 | ATATAATAGTAACAG[C/T]CCTGCCCTGCCCACC | 7464 |
rs558380723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134588 | AGACAGAAACAGAGC[C/T]TGGAGTGACGCAGCT | 7464 |
rs558395399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179146 | AACCAGCTCTTGGGC[G/T]GCTGTTTGAGTGCCG | 7464 |
rs558528387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98152092 | AAAGTGCTGAGATTA[C/T]AGGCATGAGCCACTG | 7464 |
rs558529157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176261 | TCTAATTCTTCAGTT[G/T]TTAGCCAGACCCACT | 7464 |
rs558597913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178858 | AAGCTCAAAGGATGG[C/T]AGAAATGATCTAGTC | 7464 |
rs558615106 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98159328 | GTTGGGATTAAAGGC[A/G]TGAGCCACTGCCCCT | 7464 |
rs558635076 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180420 | CATGGCTCCCCTCAC[A/T]TCACGTTTTCATCTC | 7464 |
rs558719222 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151246 | AGGGCATGGTTCTAA[C/G]GAAAAAATAGGCTTG | 7464 |
rs558749270 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142875 | CCCTGCGCTGCCCTG[C/T]GCTGCCCTGCCCTGG | 7464 |
rs558800014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131235 | CTGGTTCTTGAGTTC[C/T]AATGTGTGGGCTACT | 7464 |
rs558846087 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123774 | GATTCTCCTGCCTCA[C/G]CCTCCCAAATAGCTG | 7464 |
rs558855777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175444 | CAGCAGGGAGCCCTG[C/T]TCTGTGCAGGGAGGG | 7464 |
rs558863651 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133311 | AGTGAAACACAGTAT[C/T]CCTGGGAGGGTGGCG | 7464 |
rs558898513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181997 | CCTTTCCTTGACCGG[C/T]ACCATCTGTGCCCTG | 7464 |
rs558909723 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166455 | AGAGGAAATATTTGC[A/C]AATCCATATGATAAG | 7464 |
rs558941791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98182269 | TAACTTTTTAGGGAG[C/T]GAATGAATGGGTCAG | 7464 |
rs559004487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98133418 | TCCCAGGGCCAGGCT[A/G]TCTAGTGGTGAAAGG | 7464 |
rs559075829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151057 | TATACAGTTGCACCT[C/T]CATGCCTTTGCTTGT | 7464 |
rs559090506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140445 | ACCACTGTACTTGTT[G/T]TTTTTTTTTTTAAGA | 7464 |
rs559103691 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194453 | GTTGTTTTTGCATGG[C/T]TTTGTTCTGTCGCCC | 7464 |
rs559117552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98168163 | TAGTCACACTAGCAA[C/T]ATTTCAAGAGCTCAA | 7464 |
rs559123263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126887 | GGGCATATGGGGCAC[C/T]AATGACACAGGCAGG | 7464 |
rs559254005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98127424 | GCTGGGCTGGCCCCC[A/G]TGTTGGCAGGAGCGG | 7464 |
rs559292795 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO2A | GRCh38.p7 | 9:98147735 | GTTTCTTATAAGGCT[A/G]AACATGCAACTACCT | 7464 |
rs559324896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162539 | AAACTTCACAAGTAG[G/T]GGGTGGGGCAGCCGC | 7464 |
rs559356244 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153260 | ACCCGCTACCACACC[C/T]GGCTAATTTTTTGTG | 7464 |
rs559361574 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98167500 | TGAAATATACATATA[-/T]TTTTTTAAAAGATCC | 7464 |
rs559558992 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98142922 | CTTCTAAAAGGTTTT[-/A]ACGCTGAGGACCACA | 7464 |
rs559585072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184255 | TTTTAATAGAGGCAA[G/T]GTCTTACTTTGTTGC | 7464 |
rs559605466 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154437 | AAGAATGAAAATTAT[A/C]AGCTTAACAAATTAC | 7464 |
rs559620234 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190242 | CTCCCTAGTTACTTC[A/C]TTAGGATAAAGTCCC | 7464 |
rs559628115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182590 | CTTTTCTTTGTGGGG[C/T]TGGATGAGGAAAAAG | 7464 |
rs559679228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171097 | AGCGACAAGGATCAC[C/T]GGGGATTTTCCAAGA | 7464 |
rs559769909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176650 | TGTCCTCCCCATTTT[A/G]GTTGCCCATGTGCTC | 7464 |
rs559807781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160210 | CTGACTAATTAATGC[C/T]CATGTGATTCCAGAA | 7464 |
rs559827095 | snp | C/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194080 | ATTGCTTGAGCTCAA[C/G]AGTTCAAGACCAGCC | 7464 |
rs559847037 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98171618 | AGGGAGGGCCCCCGG[C/G]AGGATACGACTGAGC | 7464 |
rs559878595 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184939 | TGTAGTTCATAAAGC[A/G]CCTCCTTACTTTTAT | 7464 |
rs559969381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98170538 | CCTCTGCCTCTGGGG[C/T]TCAAGTGATTCTCCT | 7464 |
rs559973454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131653 | ACACCCGATCTCATT[A/C]CAATCTTCCCCTACC | 7464 |
rs559977593 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98153955 | TCCATCTATGGACAT[-/G]ATCATATGGTTTTTC | 7464 |
rs559987604 | in-del | -/C | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120566 | CCCAAATTCCAGTTG[-/C]CCCCCCCAGGCTCAA | 7464 |
rs560004740 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123130 | AGGGCAGGACTTGCA[A/G]GAGGTCACTGAGTAA | 7464 |
rs560005490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176069 | AAACTAGAAGCACAA[A/G]GTGTTCATGGTCCTT | 7464 |
rs560019476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180117 | GCGTCAGTGCTAAAA[C/T]GCTCCTCCCTGACAG | 7464 |
rs560067978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138908 | AAAAATTAGCCCGGC[A/G]TGGTGGTGCACGCCT | 7464 |
rs560075890 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142291 | GTAGGGACTTGCCCA[A/C/G]GGTCACTGCAAAGGT | 7464 |
rs560104888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179421 | TCCTGCTCCTATCTC[G/T]CATCCTCCCCATCTT | 7464 |
rs560190086 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173589 | CTGAGGCCAGCACTC[C/T]GGAACTGGGCGTCCC | 7464 |
rs560203586 | snp | C/T | 0.00043735 | 0.0147812 | intron-variant | CORO2A | GRCh38.p7 | 9:98157332 | CTCAAAGAGATGAAA[C/T]GACTTACTCAAGGTC | 7464 |
rs560249230 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122740 | GGCCCCCTACCTCCT[A/G]GGGGACTCTTCTGTT | 7464 |
rs560251694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162658 | GTGTGCGTACTGTGT[A/G]TGCACAAGAACTGCA | 7464 |
rs560327361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162138 | TTCAGGCCAGTAACC[A/G]GGTCACACAGCTAGT | 7464 |
rs560338413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129052 | ATCCTCCTGCCTTAG[A/C]GTCCCAAGTAGCTGG | 7464 |
rs560342176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135880 | TGATGAGGGCTGTCA[C/T]TGCATAGAACCCCGG | 7464 |
rs560354766 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148225 | CATAGCAAAACCCCA[C/T]CTCTACTGAAAATAT | 7464 |
rs560407478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148488 | TGCAGTGGCTCATAC[C/T]TGTAATTCCAGAAGT | 7464 |
rs560459491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135620 | AGTAAGCTCCCTGTC[A/C]CAGAGGTATACAAAT | 7464 |
rs560575128 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98182666 | TGCTGGCTGCGTGAC[C/T]TTGCAAATTTACTCA | 7464 |
rs560613922 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145752 | GAGTATTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 7464 |
rs560624788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149012 | GGGGGTGGAGGGGAA[C/T]AGATCTTTGTGATGA | 7464 |
rs560772730 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO2A | GRCh38.p7 | 9:98151878 | CTGGAGTACAGTGGC[A/G]CGATCTCGACTCACT | 7464 |
rs560810437 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161302 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 7464 |
rs560819782 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98146210 | ACCTCACAGCAAAGT[C/G]CACCTTCTTCACCCC | 7464 |
rs560853130 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120778 | TTACTATCTTTTCCT[C/T]CAGGAAGCCTTCCCT | 7464 |
rs560904589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139673 | TGGTGTCGCACACCT[A/G]TAGTTCCAGCTACTT | 7464 |
rs561041424 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159294 | TCTCAAGCAATTCTC[C/T]TGTAGCTGCCTCTCA | 7464 |
rs561060980 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132638 | TCCTTGGAGAGGAAG[A/G]ACTAACAGCCCATTG | 7464 |
rs561066538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98164027 | CCCCTTCGTAAATTT[A/G]TGGTTTCACATATAA | 7464 |
rs561104006 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98170185 | CCTTTCCTGCCCACT[C/G]TGTTTTTTCCTTCTC | 7464 |
rs561110695 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | CORO2A | GRCh38.p7 | 9:98137603 | CAGGAGGCGATCTCA[A/G]AATCATCAAAAGGGT | 7464 |
rs561132076 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136402 | TGCCTTCCTTTCCTG[A/G]TGAACTGGTCTGCTT | 7464 |
rs561149475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98136957 | TCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 7464 |
rs561153065 | in-del | -/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193746 | ATAAGAAAACTGAGG[-/C]TTGGAGTGGCAAGGT | 7464 |
rs561312560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163431 | CTGACCTCAGGTGAT[C/G]CGCCTACCTTGGCCT | 7464 |
rs561325946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98144588 | AGGCAGGAAGGAATA[C/T]ACTTTGAGCTCAGAG | 7464 |
rs561330556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175634 | TGAGGAAGAATGGAT[A/G]CAGAGGGGCTGGTTT | 7464 |
rs561353895 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187534 | CAGGAGGATGGAAGT[A/C]CAAGACTAAGACAGC | 7464 |
rs561368832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98174991 | ATAATAAAGAAAAGA[A/G]AAATGACAGCACTTA | 7464 |
rs561375286 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124172 | GCGCCTGCCACCACG[C/T]CCAGCTAATTTTTTT | 7464 |
rs561399689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98169772 | CCCAGATAATCTGTC[C/T]TTGCTCATGCCCCTT | 7464 |
rs561407981 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174423 | TCAGTCTGAACATAA[A/G]CTCTTCATTGACACA | 7464 |
rs561458181 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172942 | GGACAGGTGACAGCA[G/T]CACATTTACATGTGT | 7464 |
rs561459184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181564 | AAACGTGAGCAGACC[C/T]CTCGGCGGCCATTGT | 7464 |
rs561500070 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135945 | GATGAAGGTACCACC[C/T]GCAACACTGAAGCAG | 7464 |
rs561506480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161223 | TCATCTCAGATACCC[A/G]GACTCTGAGGGCAGT | 7464 |
rs561518438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98134359 | GCAGTGCCATCCCAT[C/T]CACTCCGGGCAGGCT | 7464 |
rs561526071 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148409 | CAAAAAAAAAAAAAA[-/AA]TAAGATAAATAAATA | 7464 |
rs561557744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133544 | GCACCTCCCACAGAT[C/T]AACAGGGCTGTATGT | 7464 |
rs561592648 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2A | GRCh38.p7 | 9:98125094 | AATAAATGAAATTCA[A/G]GAAGACTGGAATGTT | 7464 |
rs561594645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167244 | CCACTTATATGAGTT[A/G]CTTTGAGTAGGCAAA | 7464 |
rs561615239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98143866 | TCCTACTGGTGAATG[C/T]AGGCAGCTGGATCAG | 7464 |
rs561683500 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121942 | GCTAGTGCATCAGAC[A/G]GGAGTGAGCCCCAGT | 7464 |
rs561685895 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171235 | AGAGAGGAAGCGCGC[C/T]TTGCTTAGCGTCCCA | 7464 |
rs561722194 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188453 | CAGCGCCTTCCCCCT[C/T]TCCCCAGCACTTAGA | 7464 |
rs561729478 | in-del | -/AG | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173325 | TGATTCACAACTATC[-/AG]GCTCAGTTTACCCCT | 7464 |
rs561733815 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173501 | CTCAACCACCCCCCA[A/G]CTCGGTGGCCACTGC | 7464 |
rs561834289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140490 | CTGTTGTCCAGGCTG[A/G]AGTGCAGTGGTGCAA | 7464 |
rs561857317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98178821 | TTGGGATAGAAGATG[A/T]AGAGAGTCGGAGATA | 7464 |
rs561937069 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167221 | TTACAAAAAGACAGC[A/G]CATGATTCCACTTAT | 7464 |
rs562016017 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185756 | GCACTTCTTACTTCA[G/T]CCTGTGGCTGGGGCC | 7464 |
rs562180867 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194050 | CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGTGGA | 7464 |
rs562203758 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98160248 | AAGAAGACTCACAAA[A/T]ATAGAACACAAGATA | 7464 |
rs562208195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171716 | CTGTGCTAGGTCATG[A/C]CTGTCTGTGGTGTGC | 7464 |
rs562250466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166160 | CACAGATACAATCAG[A/G]AAAAAAACACAGGAC | 7464 |
rs562265415 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193510 | AGCTAACAGCCACTC[C/T]ACTCCACACCACGTC | 7464 |
rs562310748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126325 | AAGAGTGAGCCACTG[C/T]GCCCAGCCTCCCACC | 7464 |
rs562333289 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148939 | GTAACATTCCTAAAA[C/T]GGGAAAAGTATAGAA | 7464 |
rs562345916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132730 | AAACAGTGGTATCGT[C/T]GGCTCTCCTGACCCC | 7464 |
rs562352087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125552 | GAGAGAATTCAATCA[C/T]GTGCTGTATCAAAGT | 7464 |
rs562396418 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183426 | GCACTGGGGATGTCA[C/T]CCAGGCCTTACCAAA | 7464 |
rs562402579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98157851 | TCTGTAGACCTGGTA[A/G]GATAAGATGGGATGA | 7464 |
rs562409793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171164 | CCTGCTCACTGTCCG[C/T]TTTCTGGCACAGAGC | 7464 |
rs562501567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187568 | TTTGGAGTCTGGTGA[C/G]GGCCCACTTCCTGGG | 7464 |
rs562646170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168746 | AGGTATATGCTGGGA[A/G]GCCAGCATTTTGGGT | 7464 |
rs562678488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98149597 | TGTGCCGCAGGCCAC[A/G]GGGAGGTGTCCCAGA | 7464 |
rs562713829 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136380 | CACAAATCCTCTTTG[A/C/T]ATTTTCTGCCTTCCT | 7464 |
rs562754440 | snp | C/T | 1.64819e-05 | 0.00287066 | intron-variant | CORO2A | GRCh38.p7 | 9:98129784 | ATGAACTTCAGTGTC[C/T]CTCACTTACCGATCC | 7464 |
rs562800713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155551 | GGGGTTTCACCATGT[C/T]GGTTAGGCTGGTCTC | 7464 |
rs562840106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129193 | CCTCCCAAAGTGCTG[A/G]ATTAGCTGAACTTTT | 7464 |
rs562842911 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188013 | GCAGGATTCCATTAT[A/G]AGCATGGTGGGGTAC | 7464 |
rs562846975 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98143123 | ACGCCTGCTCCCCTC[A/G]CAGACCCCACAGAAC | 7464 |
rs562877711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98142134 | CAAAAACTTCTGTTA[C/T]AAAACTGTAGCTCTT | 7464 |
rs562913847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135686 | ATCTTCCTTATTGGT[C/G]CTGCAAGGTTCTCTG | 7464 |
rs562929197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171757 | CCAGGAGCTTGCAGC[A/G]CGGGGGTGGGGAGGC | 7464 |
rs562968956 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141084 | TCTGAAAACAAAAAA[C/T]TATACACACACCTAC | 7464 |
rs562999111 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98142608 | GAGCCAATAGTCAGG[C/G]TGCCCTCGGGCTGAC | 7464 |
rs563023893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192329 | CCCTCCCAACAACCC[A/C]GCGAGAAGGGGGCCA | 7464 |
rs563075304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147020 | GCCTGTTATCCCAGC[A/C]CTTTGGGGGGCTGAG | 7464 |
rs563200485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152335 | CGCTTTGTCACCTAG[A/G]CTGGAGTGCAGTGGC | 7464 |
rs563225863 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | CORO2A | GRCh38.p7 | 9:98150324 | CCTTCACAGTCCAGG[-/C]CCTACTCCCCAATCT | 7464 |
rs563232090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139870 | AAAGGGCATTTCCCT[C/T]ATTTTCCCCTTTCCT | 7464 |
rs563236645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161619 | CAGATTTAATTTTCA[A/G]GTTTTCCTCTGATTC | 7464 |
rs563248808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183559 | ATAGTTGGCCCTCTG[C/T]ATCTGTGGGTCCTGC | 7464 |
rs563277361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178078 | TAGAGACAGAGTCTC[A/G]CTCTGTCGCCTAGGC | 7464 |
rs563423928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98124990 | CCCTCTTTGACTCAG[A/G]AAGGTGGAGGCGGTC | 7464 |
rs563431215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139358 | TTAGGCCTGGCATGG[C/T]GGCTCACGGCTGTAA | 7464 |
rs563452362 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174146 | ACAAAAAACAAAAAA[A/C]AAAAACCAAAGAGCG | 7464 |
rs563478486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159542 | CTCTGGCTCTTTGCC[C/T]GTCCCTCTCCTTCTG | 7464 |
rs563511927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189237 | CAGGAGGCACAGTTT[A/G]ACCACAGAAGCAAAG | 7464 |
rs563739538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171080 | CTTATCTGGGAGTTT[C/T]GAGCGACAAGGATCA | 7464 |
rs563771300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164236 | AATCAGGATAAAGAA[C/T]GCTCTATGTGAAGGT | 7464 |
rs563788677 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122589 | ACAGATTCACTAAGG[A/C]GGGACAAAGAAAAGC | 7464 |
rs563807028 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98170915 | CACACACAGGACCAC[-/A]AGGGCGACAGAGCTG | 7464 |
rs563813709 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173164 | ACAAACAAACAAACT[C/T]CGATTGTTGGGCCCC | 7464 |
rs563870163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98157719 | TGATCATGGGACACA[C/T]AGAGCTCTCATCTTA | 7464 |
rs563898087 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124162 | GGAATTACAGGCGCC[C/T]GCCACCACGCCCAGC | 7464 |
rs563942151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155647 | ACCACGCCTGGCCTA[C/T]TGTTCAATTTTTAAA | 7464 |
rs563943651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98175156 | GCAGGGGGTGGGGTG[C/T]GGGATGGCCCTCCCT | 7464 |
rs563982454 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98142524 | CACTGATTGCTCTCC[C/G]GGCCTTTAGACTCTG | 7464 |
rs563983171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98161783 | CCTGAGTGCATGTGG[C/T]GGGCCTGGGGTAGTC | 7464 |
rs564002015 | snp | A/C/G | 4.94208e-05 | 0.00497075 | missense | CORO2A | GRCh38.p7 | 9:98137672 | ACTTTTGGGTAGTGG[A/C/G]GGTCCAACTTCCCTG | 7464 |
rs564018467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181692 | TGGCAAGGCTGTTTC[C/T]CCTATGCAGCGTGCC | 7464 |
rs564051631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98185152 | CAGCTCCTCTAGGGA[A/G]CCTTCCATGACCCCC | 7464 |
rs564090801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162107 | GCTACCTTGCTCCCC[C/T]GTTCAGATGTAGGTG | 7464 |
rs564136686 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98127577 | AGCACTTCGGGAGGC[C/G]GAGGCAGGTGGATCA | 7464 |
rs564176184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190817 | CTTAAGCCTGTGCGT[C/T]GGAGCTGGGCTCATG | 7464 |
rs564221027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134458 | GGAAATGGGGTCTTC[A/G]CTGCTGAAATTAGTT | 7464 |
rs564229015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178877 | AATGATCTAGTCTAC[C/T]CTTCACTTTGCAGGT | 7464 |
rs564255745 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173545 | GGCTTGCTTTCTTAA[A/G]TCTCTTCTCAACATA | 7464 |
rs564260429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190508 | GATCCCTGGGCTCGG[C/T]TGCTGGTTTGCTGTG | 7464 |
rs564341946 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173013 | AGTCACCTGGAGGGC[G/T]GGAAAAAAACAAACC | 7464 |
rs564380129 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186674 | TACATATAATATATC[C/G]ATTTTAAAACGGGAG | 7464 |
rs564396465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166326 | ATTCCTTGGTTATGA[C/T]ACCAGGAACAGGCAA | 7464 |
rs564405769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141245 | ACAGGGGAGAGAGGT[G/T]CATGCTTCCTGCCCT | 7464 |
rs564453769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98154113 | GGCATCCATCTTCAT[A/G]AGTGAGATTGATCAA | 7464 |
rs564487307 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | CORO2A | GRCh38.p7 | 9:98172140 | CCCTGGGACAAGAGT[A/C]CCCAGATATGACTGA | 7464 |
rs564533019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188895 | AATGAATGAACATAA[A/G]GCACTTAGGACAGAA | 7464 |
rs564534933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98182120 | CTACGATTACTGTCC[A/C]TCTCTCGTTTGGTCT | 7464 |
rs564564219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147812 | AGACTTACTTATATT[C/G]ACCCAAAAATATGTA | 7464 |
rs564573541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98188447 | TAATATCAGCGCCTT[C/T]CCCCTTTCCCCAGCA | 7464 |
rs564659883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187572 | GAGTCTGGTGAGGGC[A/C]CACTTCCTGGGTCAT | 7464 |
rs564759740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163891 | TGAACCCAAACTGGG[C/G]GTGGTGCAAACCATT | 7464 |
rs564796540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163211 | TTTTTTCTTTGAGAC[A/G]GAGTCTCGCTCTGTT | 7464 |
rs564821984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151732 | CAATGGCGCCATCTC[A/G]GCTCACTGCAACCTC | 7464 |
rs564842800 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138555 | GCAGAATACTACTGT[A/C]CCTAAAAAGAGGAAT | 7464 |
rs564863514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158812 | GGTTTAGTAAGATTA[C/T]CAAAGAGAAATTAAA | 7464 |
rs564882173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169650 | TCCTTCTCATCTCCA[C/T]AGACCTGTTCTCTGA | 7464 |
rs564882606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162785 | TGCATGAGCGCATGC[A/G]TGTATCCGTGCATGC | 7464 |
rs564922323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169139 | AGCGAGGCAGAAGCC[A/G]TCTGCAGCCGGCAAA | 7464 |
rs564965591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144808 | GGCTGGAGGACAGGG[A/C]AAGAGAGGAGGCTGA | 7464 |
rs565016377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136775 | TGATAAGTGTGATGA[C/T]AGTTAGGAATACAGT | 7464 |
rs565021631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151332 | GTCTATCCATGAATA[C/T]AGTAAATATTTCCAT | 7464 |
rs565048484 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194149 | AAAAATTAGCCGGGC[A/G/T]TGGTGGCATGTGCCT | 7464 |
rs565063006 | in-del | -/GAGA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163742 | TGTATGTGTGTGTGT[-/GAGA]GAGAGAGAGAGAGAG | 7464 |
rs565231707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149889 | AGAATCACACATTTT[A/T]TCTAGGATCAGGCTG | 7464 |
rs565387331 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137379 | AAGGCCCATAGAGAG[A/G]AGGGGTGGTGCCGCT | 7464 |
rs565391187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181181 | CTTGTGTCCCCCAGC[A/G]CGACTCCCTCTGCAA | 7464 |
rs565401395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165488 | ATTCTGCGCCAAGCC[A/G]TGTCAGGAGCAGGGC | 7464 |
rs565469278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98189773 | TTCTATGCTGGCCAG[A/C]CTCCGGTAATGTAAG | 7464 |
rs565472126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186817 | CCCAGGGTCAGCCTG[A/G]CTTCCTCCTCATCCT | 7464 |
rs565500381 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CORO2A | GRCh38.p7 | 9:98132934 | CTGTGAAGGCGCAGC[C/T]CAGACGCTGACAGCA | 7464 |
rs565511755 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186123 | CTAGAAGCAGCTGTC[A/C]TATCAACCCTGCACA | 7464 |
rs565597538 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | CORO2A | GRCh38.p7 | 9:98192457 | GCTCCGAGCCCCGCA[A/T]CCCTCCCTCTCCGGG | 7464 |
rs565608892 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123447 | TGGAATACAGTGTGG[A/G]GAAGGGAGACACAGC | 7464 |
rs565625583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98139411 | GATGGGTGGATCACC[C/T]GATGTCAGGAGTTTG | 7464 |
rs565641877 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121752 | ATGGGGACTGTAATG[C/T]CTGCCTGACCTGTGT | 7464 |
rs565645268 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125792 | GTGTGATCCTGGCTC[A/G]CTGCAGCCTCTGCCT | 7464 |
rs565663571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138787 | GGCGCGGTGGCTCAC[A/G]ACTGTAATCCCAGCA | 7464 |
rs565704592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126114 | GATCTTGGCTCACTG[C/T]AACCTCCACCTCCCA | 7464 |
rs565748185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126434 | AGTGACTAGGCCAGG[C/G]CACACAGCTGGTTAT | 7464 |
rs565749317 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98145751 | AGAGTATTGCTCTGT[A/C]GCCCAGGCTGGAGTG | 7464 |
rs565769772 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | CORO2A | GRCh38.p7 | 9:98171764 | CTTGCAGCGCGGGGG[G/T]GGGGAGGCTGGGTCT | 7464 |
rs565849656 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151413 | TCTAAGCGTTGCTTG[C/T]TTATTCCTAGGTATC | 7464 |
rs565857780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177627 | ATGTGCCACCACACC[C/T]GGCAAATTTTTTTGT | 7464 |
rs565953473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131957 | CTCTAGCCAACGGAC[G/T]CCCCTGGGTCCTGAC | 7464 |
rs565980315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176370 | CACCCCACGTAAACA[C/G]TCTGATGGTTTTGGC | 7464 |
rs565992725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146437 | CCTGCAGTGTCACTC[C/T]CTTTGGGACATCTGA | 7464 |
rs565996553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183088 | ATCTCCAGAGCTTCA[C/T]GGAATTTGAAGGCTC | 7464 |
rs566078827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152478 | CATTTTTTGTAGAGA[C/T]GGGGTTTCTCTATGT | 7464 |
rs566122119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98188712 | GAGGCGGAGGTTGCC[A/G]TGAGCCGGGATCATG | 7464 |
rs566226362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159043 | CTCACCACCCCACCC[C/T]CACCTCATATCACCC | 7464 |
rs566230076 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194465 | TGGTTTTGTTCTGTC[A/G]CCCAGGCTGGAGTGC | 7464 |
rs566239628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158387 | TGGTGCATGGCAGAT[A/G]CTTGATCAACAGTGG | 7464 |
rs566264453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164242 | GATAAAGAACGCTCT[A/G]TGTGAAGGTGCTCTA | 7464 |
rs566301690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125017 | GGTCACATTAACATG[A/G]CTGAGGCCTGATGGG | 7464 |
rs566350434 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98163713 | GACATACATGCGGGG[G/T]GTGTGTGTGTGTGTG | 7464 |
rs566368449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149946 | CTTTCTTTTTTTTTT[C/T]TGAGAGAGTCTCGCA | 7464 |
rs566384497 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98192666 | CCGCCGCCGCCTCCC[C/G]CTGCAGCCCGGCGGG | 7464 |
rs566432039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98179810 | GAGTTTGAGACCAGC[C/T]TGATCAACATGGTGA | 7464 |
rs566485491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142246 | CAGCACCCTCTCTCG[A/G]ACCTCAGACTTGGGG | 7464 |
rs566523223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98149375 | TGTAACACTAAAGTA[C/T]GAGAAGCTCTGATTA | 7464 |
rs566612648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168213 | ATCACAGATGAAACC[A/G]TACAAGCAACACCCA | 7464 |
rs566625403 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2A | GRCh38.p7 | 9:98183892 | CTTGAACCCGGGAGG[C/T]GGAGTTTGCAGTGAG | 7464 |
rs566648654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161869 | TGAGCTGTCTCCCTC[C/T]ACAGCCTGTCTGTGC | 7464 |
rs566680087 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180295 | TTCCTTTGCCAGTAA[C/T]GCCCTATCCACCACT | 7464 |
rs566757023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127289 | ACTCGGCCCTGGTCC[A/G]CTGCCCCCCAAGGCA | 7464 |
rs566759623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167755 | TTATATTAGACAAGA[C/G]TCTTTATCTTTTAGA | 7464 |
rs566777710 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98172587 | AGCTCGACCCCACAG[A/C/T]GGGAAGTGGATGGGA | 7464 |
rs566835836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141626 | TCCAAAGTGCTGGGA[A/T]TATAGGCTTGAGCCA | 7464 |
rs566871837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98160794 | CCCCTCATGTCCAGG[C/T]CCCTTCCAGTCAGGC | 7464 |
rs566873389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134523 | ATCCAATGATAGTTG[C/T]TCTCCTCTTCCTATA | 7464 |
rs566960620 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98133899 | GCTGGGACTACTTGA[C/G]GCATTTTCCCACACC | 7464 |
rs566960716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141335 | TGGCCCAGGTCTCCA[A/T]GGGACCACTGACCCT | 7464 |
rs566997529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98140708 | ACTTGCCCTCCTAAA[A/G]TTAGGGATTACAGGC | 7464 |
rs567033265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189957 | TGGCACAATCTCGGC[C/T]CACTGCCACCTCTGC | 7464 |
rs567039008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98175335 | GCCCCTGGCAGAGTC[A/G]TGGCTCTTCCCACCA | 7464 |
rs567068290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147828 | ACCCAAAAATATGTA[A/C]ACAAATGTTTGTAAC | 7464 |
rs567089865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98153402 | CAGCGCATCCGGCTG[A/G]TAACTTTTTTTTTTT | 7464 |
rs567096539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190596 | GGGGGTTGAATGAGA[C/T]GACGTCTGAAGGCTC | 7464 |
rs567284665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169988 | GGAGGTAGCCAAAGG[C/T]AGGGAAAAAGAAGGC | 7464 |
rs567365208 | snp | A/G | 0.000105578 | 0.00726483 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98131048 | CTCCATCAGAGGCAC[A/G]GAGAGGTTATCCTGC | 7464 |
rs567370657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144850 | GAGGCTGAGGGCATG[C/G]AGTCTACTCACCCTG | 7464 |
rs567404198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137947 | ATGGGAGAGGAGGTA[C/T]GGCACAGTGCCTAGC | 7464 |
rs567409111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151381 | TTAGTCTTTTAACAA[C/T]GTTCTATCATTTTCC | 7464 |
rs567522850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129490 | CTTTCCATCTCTGCT[C/T]TTGTGGTAACTGCTT | 7464 |
rs567528455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187174 | TGTAGTCCCAGCTAC[G/T]GGGGAGGCTGAGGCA | 7464 |
rs567597420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150872 | TGTCCCTCCCTAGCT[C/T]GAAACATTCTCTCTC | 7464 |
rs567614252 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193641 | GGATAACAGAGTACA[C/T]TGTTACTACTTTACA | 7464 |
rs567736146 | snp | A/G | 1.65211e-05 | 0.00287407 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126798 | CAGCAGCTCAGAGCC[A/G]GGCCTAAGGGACACC | 7464 |
rs567771618 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130223 | GTAGGTGGGACCACA[A/G]GTGTGTGCCACCACG | 7464 |
rs567790765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98148648 | ATTCAGGAGGCTGCC[C/G]TAAGAGGATTGCTTG | 7464 |
rs567814068 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122981 | CCCCTTGCCAGTGTC[C/G]GTTAGTTTCTGTAGC | 7464 |
rs567836644 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98170536 | AACCTCTGCCTCTGG[G/T]GTTCAAGTGATTCTC | 7464 |
rs567875084 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174144 | AAACAAAAAACAAAA[A/C]AAAAAAACCAAAGAG | 7464 |
rs567881125 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192023 | GTAAACCCTCTTGGC[A/G]GGCCGGCTGATGCCC | 7464 |
rs567899515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142707 | GCCTTAGGGTTGGGC[A/G]TGGCTCAGAAGGGCC | 7464 |
rs567900972 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125494 | TCTGTGAGATGCCAG[C/T]CTCTGTGTTCTTAGC | 7464 |
rs567921816 | snp | A/C | 0.000133169 | 0.00815885 | missense | CORO2A | GRCh38.p7 | 9:98126555 | CCTTCACACCTCATT[A/C]TCTGTCTTTGGTGGG | 7464 |
rs567951621 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98167567 | TCATTACAGTTCAGA[-/AG]AGACTTAAGAGATCA | 7464 |
rs568026151 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123352 | TCACTAGCTTTCAAA[C/G]TTCTAAAAAAATTTT | 7464 |
rs568051082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132405 | CCGCTCCACCTGGGA[A/G]GCCTCCCTTTCTCAC | 7464 |
rs568053216 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98151252 | TGGTTCTAAGGAAAA[A/C]ATAGGCTTGGAATAT | 7464 |
rs568068769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98160516 | CAGCACATCTTTTCT[C/T]TATAGTGAGTTTTGA | 7464 |
rs568255365 | snp | A/G | 0.117537 | 0.212022 | intron-variant | CORO2A | GRCh38.p7 | 9:98172450 | CCACACCCCACTTCC[A/G]AGCTCAGCCCCACAC | 7464 |
rs568264241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98165363 | AGGGCCCAACATACC[A/G]AACCATAGAATAGAA | 7464 |
rs568380361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140064 | TCTGCTCATTTTGCA[C/T]ATCACATTGCATGGC | 7464 |
rs568386231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98139501 | GCGTGGTGGCACATG[C/T]CTGTAATCCAAGCTA | 7464 |
rs568402739 | snp | A/T | 0 | 0 | intron-variant | CORO2A | GRCh38.p7 | 9:98183135 | TGGCGCCCCTCTGGA[A/T]CTGTCTCAGCTGTCC | 7464 |
rs568422607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146496 | AGAAGGACTTCCTGC[A/G]CGCTGTGGCAAGGCC | 7464 |
rs568438966 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98189427 | AACTTCTAAAACGAT[A/C]CAGCTTCTGGCCATT | 7464 |
rs568463949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98147227 | CAGGGACCATTAACA[C/T]GAATTAGGAATCAGG | 7464 |
rs568482762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98189811 | GCCACTATTTTTTAA[A/G]CTGTATTTGTCAAAT | 7464 |
rs568590578 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185305 | GTCTGCATTCACACT[C/T]CCCAAGCATTAGAAA | 7464 |
rs568664352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164395 | GCTGGGAAAGCTCTT[C/T]TCAGTCATCCAGAAT | 7464 |
rs568704055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165070 | ACCTCCTGGGCTTGC[A/G]CAATCCTCTGGCTTC | 7464 |
rs568755384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181329 | CAAATCATCTCTCTC[G/T]CTTGCTTTTTTTTTT | 7464 |
rs568760013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191964 | CAGTCGTGCCGCCAG[A/G]AGTCCAGCCACCTCC | 7464 |
rs568855108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135896 | TGCATAGAACCCCGG[A/G]AGGAAGACACACTCT | 7464 |
rs568864168 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174151 | AAACAAAAAAAAAAA[A/C]CCAAAGAGCGTGTAG | 7464 |
rs568885754 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142274 | GGGAAATCCAGCATG[C/G]AGTAGGGACTTGCCC | 7464 |
rs568893720 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98142946 | GACCACAGGCAGGAG[A/C]GGACATTAGCCAGCC | 7464 |
rs568957936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186350 | GACATTCCAGGGATG[A/G]ACTACAGGCAGCAGG | 7464 |
rs568965998 | in-del | -/AAACA | 0.0239027 | 0.106677 | intron-variant | CORO2A | GRCh38.p7 | 9:98180003 | GTGAGACTCCATCTC[-/AAACA]AAACAAAACAAAACA | 7464 |
rs569012466 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144780 | GAGGCTGAAGCAGCC[A/G]GCGGGCACGGTAGGC | 7464 |
rs569017059 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173295 | TTGAGAATCGCTGCT[C/T]TACAGCCCAGCTCTA | 7464 |
rs569025247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98179480 | TCCTCATCTCAGATC[C/T]CACCTCTCTAAAGCT | 7464 |
rs569104442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179096 | GGGTTCACTCTGAAG[A/C]CTCAGTTTCCTCATC | 7464 |
rs569143402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98155992 | TCATTGATTTTTGCT[C/T]TTTATTATCTCCTTC | 7464 |
rs569159250 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157783 | TCAGTTCAACGTGGA[C/T]GGTGATGCACTGTGA | 7464 |
rs569200657 | in-del | -/AAACA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180002 | GTGAGACTCCATCTC[-/AAACA]AAACAAAACAAAACA | 7464 |
rs569223327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167880 | TGCGTAGAGATGAAA[A/C]AGGCTGCTGATGGCT | 7464 |
rs569227831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168315 | CCTATCTGCCACTCT[C/G]GGCAAGTTACTTAAT | 7464 |
rs569252685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98135057 | AGCAGAAGGACCAAG[A/G]GAGCTCTCTCCATAG | 7464 |
rs569256218 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98148007 | ATCCTGGCACTTTGG[G/T]AGGCTGAGGCAAGAG | 7464 |
rs569284754 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121669 | AACCCCACCTCTACC[A/G]CTTGGCAGTCAATGA | 7464 |
rs569373198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127711 | CCCAGCTACTCAGGA[A/G]GCTGAGGCATGAGAA | 7464 |
rs569419967 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98170829 | GTTTCTATCCATATA[A/C]TAGTAACAGCCCTGC | 7464 |
rs569455042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141434 | CCGGATCACTGCAAC[A/C]TCCACCTCCCAGGTT | 7464 |
rs569474492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184511 | ACTCTTTCTCTTACC[A/G]TGACATGGTGGCCCT | 7464 |
rs569571845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145618 | GAGAGAGGCAGAACA[C/T]TATCTGCAGGCAGCA | 7464 |
rs569643912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144923 | GATAGGTGAGCCATG[C/T]CCTGACTGGAGAGGG | 7464 |
rs569658848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151912 | AGCTCTGCCTCCCGG[A/G]TTCACGCCATTCTCC | 7464 |
rs569677618 | snp | C/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194435 | CTGAATAACTTTGTT[C/G]TTGTTGTTTTTGCAT | 7464 |
rs569703962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164439 | CTGATCCACCCATTG[C/T]GAGTGGGATATCTGG | 7464 |
rs569740821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98176805 | CCCAAGAGATCGTGG[C/G]GTACAGAAAGAGGAA | 7464 |
rs569745339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98176223 | CCTTATCAACCCATG[A/G]GTGTTGATTTAGAAT | 7464 |
rs569765967 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98125156 | TGAAATAGAGGAAAG[C/G]ATGCCTGGCTCTGAA | 7464 |
rs569817759 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129579 | TCCTCCAATGTTGCC[A/T]CCTCTGAGAAGCCTT | 7464 |
rs569889434 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124332 | CTGGTTTCAAACTCC[A/C]GACCTCAAGCAATCC | 7464 |
rs569991677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187685 | CCATTATGAGGGCTC[C/T]GCCTTCCTGACCTAA | 7464 |
rs570004935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98151689 | TTTTTTTGAGACGGA[A/G]TTTTGCTCTGTCACC | 7464 |
rs570009581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98158250 | CAGGAGTTCAAATGT[A/G]GCCTGGGCAACACAG | 7464 |
rs570049270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129580 | CCTCCAATGTTGCCT[A/C]CTCTGAGAAGCCTTC | 7464 |
rs570213710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98162894 | TGTAGCGGGCCCTTC[A/G]CCTACAGGCTGGGCC | 7464 |
rs570245541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98169869 | GCCCCTTCCTGTCAC[A/C]CCACCTTCCTGGCCC | 7464 |
rs570285552 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120993 | TAGTAAAATGGCCAG[A/G]TGTTTATTATTTTGT | 7464 |
rs570334090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98169302 | ACCAAGACAAGGCCT[C/T]TTTCTTCCTGATGAG | 7464 |
rs570390470 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187748 | TCACCTTATGGGGTA[A/G]GATTTCAACATATGA | 7464 |
rs570508086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191148 | GTGATTCCTAGAAAC[C/T]GCTCCCTCAAACAGG | 7464 |
rs570573731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161333 | CTGAGGTGGGGGGAT[A/C]ACTTGAGGTCAGGAG | 7464 |
rs570614140 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98177289 | AGATAGCCCCTGTGC[G/T]GGGCTCTGTGGATGG | 7464 |
rs570643750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167570 | TTACAGTTCAGAAGA[G/T]ACTTAAGAGATCAGA | 7464 |
rs570656684 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98150045 | CAAGCAGTTCTCCTG[C/T]CTCAGCCTCCCGAAT | 7464 |
rs570700541 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148263 | AGCCAGGTGTGGTGG[C/T]ATGTGCCTGTAGTCC | 7464 |
rs570721033 | snp | G/T | 3.29473e-05 | 0.00405864 | missense | CORO2A | GRCh38.p7 | 9:98126616 | AGCCAGGTTTTCTTC[G/T]CCTCCAGCCTGTGTT | 7464 |
rs570731602 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160227 | ATGTGATTCCAGAAA[G/T]GATTTAAGAAGACTC | 7464 |
rs570732662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98166606 | TATGAAAGATAGTAC[A/G]GCAGTTCATCAAAAA | 7464 |
rs570792717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177828 | CTCGCAAGACAAAAC[A/G]TATACACAGAGTGAG | 7464 |
rs570824329 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98178278 | TATCAAACTCCTAGC[C/T]TCAAGTGATCCTCTC | 7464 |
rs570858894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171947 | TAGGAAGTCAGGACA[C/T]TGAGCCTGGGAAACG | 7464 |
rs570863156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98140602 | GCATGTGTCACCAAG[C/T]TCAGCTAATTTTTAA | 7464 |
rs570876368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98183886 | GAATCACTTGAACCC[A/G]GGAGGCGGAGTTTGC | 7464 |
rs570945160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181714 | CAGCGTGCCTCCCTC[C/T]CCACCCTTGCCTGCT | 7464 |
rs570987957 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98147400 | ATACTTCAGGTAAAA[G/T]GGATGAGTGAAGCAA | 7464 |
rs571011325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152731 | ACCACCACTCATGCA[A/G]TATTCTTGCCAAAAA | 7464 |
rs571064187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187103 | GCTAACACTGTGAAA[A/C]CCCGTCTCTACTGAA | 7464 |
rs571083661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98160343 | TCACCTGAAACGCAG[A/G]AGGAGTTAAGCTAGG | 7464 |
rs571119888 | snp | C/T | 0.0011988 | 0.0244533 | intron-variant | CORO2A | GRCh38.p7 | 9:98130951 | CCTCCCGTGCCAAGC[C/T]GACCTTCCCCACCAC | 7464 |
rs571151639 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193553 | TTGGTTTTGTTCAGT[A/G]GAGACGGGTTATCTT | 7464 |
rs571151678 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186527 | ATATTGATTATGTGG[C/G]ATGAGAAGAGGAGAA | 7464 |
rs571186842 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123778 | CTCCTGCCTCAGCCT[C/T]CCAAATAGCTGGGAT | 7464 |
rs571227973 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98130192 | CTCAAGCCATCTTCC[A/C/T]GCCTCAGCCTCCCGA | 7464 |
rs571248479 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174702 | CTGCGAGTTATCTCC[C/T]TCCTGCAGCCCTGTG | 7464 |
rs571262069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98169459 | ACCCCTCTCCCAGGC[A/C]ATGCCAAGGCCTCAG | 7464 |
rs571268542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137813 | GCTGGGTGTGAATCT[A/T]GGCCTTACTTCTTAT | 7464 |
rs571290209 | in-del | -/AAACA | 0.221054 | 0.248319 | intron-variant | CORO2A | GRCh38.p7 | 9:98180007 | ACTCCATCTCAAACA[-/AAACA]AAACAAAACAAAACA | 7464 |
rs571352363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137259 | ATGCCCCTCATAGCC[C/T]TTTATAGCTCCCCGA | 7464 |
rs571361614 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138939 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7464 |
rs571382098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98162004 | TCACAGTCACCTCTG[C/T]GGCAATAAGAAGTCA | 7464 |
rs571420475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168380 | CAAATACACATACTA[C/G]CTAACGCCTATATTA | 7464 |
rs571472200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150180 | TCGTGATCTGCCTGC[C/T]TCGGCTTCCCAAAGT | 7464 |
rs571627574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129346 | CAGTCCCTTACTTTT[A/G]ATCTAGCCATGTCTT | 7464 |
rs571651814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98130673 | CTACCCAGTGGAGAC[A/C]TGTTCTGCCCCCAGT | 7464 |
rs571661124 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174478 | GAGTAGGCTACTGTG[A/G]AATCAAAATGTAAAA | 7464 |
rs571662396 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174084 | TGCACTCCAGCCTGG[A/G]CAACGAGAGTGAAGC | 7464 |
rs571671366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98182650 | GCCCAGCTTTGCCTC[C/T]TGCTGGCTGCGTGAC | 7464 |
rs571708251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98188910 | AGCACTTAGGACAGA[A/C]TTAGGCAGGCGGTAA | 7464 |
rs571709369 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122820 | ACCTGAGGGCCTTGG[C/T]GGTGGCAGTCAGCAG | 7464 |
rs571712386 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186675 | ACATATAATATATCC[A/G]TTTTAAAACGGGAGA | 7464 |
rs571745146 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122296 | ACCATACAGGCCCTA[A/C]TCTGGAGATTCAGCT | 7464 |
rs571765111 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172091 | AATTCTGAGGCCTTC[C/T]GTGCTTGGACTCAGG | 7464 |
rs571776662 | snp | C/G/T | 4.94319e-05 | 0.00497127 | synonymous-codon, missense | CORO2A | GRCh38.p7 | 9:98128634 | AATCATGGAGATGGG[C/G/T]TCGATGAGGCTTTTG | 7464 |
rs571809126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159356 | CCTGGCCTCACATCA[C/T]CCTCTGATGCTGCCC | 7464 |
rs571866432 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173449 | CGATTAATAAGCAGC[A/C]GGAACTCCTGTCCAA | 7464 |
rs571898201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98164510 | GCCAACCTAGGCCTC[C/T]GGGTAACCATTTCCC | 7464 |
rs571898525 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CORO2A | GRCh38.p7 | 9:98158861 | CACACACACACACAC[A/C]ATGTATATTGGGTAA | 7464 |
rs571934071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98146147 | GGTTCCAGGGCTGAC[C/T]CCCAGGGGCTCTGCC | 7464 |
rs572020053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152103 | ATTACAGGCATGAGC[C/T]ACTGCACCCGGCCTC | 7464 |
rs572122228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138276 | AAAAATTAGCCGGGC[A/G]TGGTAGCATGCACCT | 7464 |
rs572137396 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170296 | CTGTGGGTACCCAGG[G/T]GGAGGCCAACCTGAC | 7464 |
rs572242176 | snp | A/G | 0.000203978 | 0.0100969 | missense | CORO2A | GRCh38.p7 | 9:98124860 | GGGTCAACAGCTCCC[A/G]GAGCCTTCGGATCTC | 7464 |
rs572264518 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98170115 | ATGTATGTAAAAGAC[C/G]TTGCATGTGTCTGGC | 7464 |
rs572279206 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98131354 | TTTTTTTGAGACAAG[G/T]TCTAACTGTCACCCA | 7464 |
rs572301597 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98175551 | CCTCTCTGGGCTCCA[C/G]TGTCTCAACCCATTA | 7464 |
rs572389840 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152212 | GGCTTTCTGTTTCTA[C/T]TTGAATTGGTATTGA | 7464 |
rs572491209 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134334 | CAGGGTCGGGGGAAC[A/G]ATTTTCTGGGCAGTG | 7464 |
rs572529399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134754 | TTTCCATTGTATTCC[A/G]GTTTGTGGGAACTTG | 7464 |
rs572552370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181555 | GAAATATGTAAACGT[G/T]AGCAGACCCCTCGGC | 7464 |
rs572644901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187438 | CACTCCAGCCTAGGC[A/G]GCTGGGCGAAACTCC | 7464 |
rs572674343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98150515 | AAAGATCACCTTCCC[A/G]GGAATGCCTTCCCAG | 7464 |
rs572679724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98164882 | AGGCAGGACTTACAG[C/T]GCTAAACTGGGGGAA | 7464 |
rs572792477 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172915 | CACTTCTGCCCGCAA[A/G]ACTGGCTGTGAGGAC | 7464 |
rs572810921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141715 | TCAAGGTGAGTTTTC[A/G]AAAATTAAAACCTGA | 7464 |
rs572901079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148816 | ACAAAACACAAAAAA[A/G]AATGATCAATACTCA | 7464 |
rs572917967 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98179259 | GGACCGCTAGAGCAT[A/G]AGGATTCTGCCTCTG | 7464 |
rs572997499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190774 | CCAGATTATACATGT[G/T]TCGAGATGACAGGAG | 7464 |
rs573039451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184585 | CCCGTCCTCTATCCC[C/T]ATCCCTGGCAGGTCC | 7464 |
rs573052127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177910 | ACATAAACAAACAAA[C/T]AAACTTGAGCTGACA | 7464 |
rs573148656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98154715 | AGTTTAAAATTTGTT[C/T]GGCTTATTTCACTCA | 7464 |
rs573177321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98160969 | GGTGCATGTTTCAGA[C/T]GGTGCATCTATAAGG | 7464 |
rs573279068 | snp | C/T | 4.94303e-05 | 0.00497119 | missense | CORO2A | GRCh38.p7 | 9:98126740 | GTGAGGCTGGGGCCA[C/T]GGAATTGAAGATAGG | 7464 |
rs573290350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126298 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAAGA | 7464 |
rs573301495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98172017 | ATAAGTGGGTTTCAT[C/T]TCATGTCCAGCTCCA | 7464 |
rs573310995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98171700 | CATGGGGTGGAAGGC[A/G]CTGTGCTAGGTCATG | 7464 |
rs573391075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165290 | ATTGTAAATTCCTGG[C/T]AGCCCTGACTTTGTC | 7464 |
rs573400419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98177143 | CTCCAGAGAGTGCTT[C/T]AGGCTGGGAATGATG | 7464 |
rs573418323 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127117 | GACCTTGCCCTTGCT[C/T]TGTAAGGACAGTCCC | 7464 |
rs573498938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132511 | TCTTTGTTAAGAGTT[A/G]TTTTTCTGAGCAAGA | 7464 |
rs573572566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98163806 | TTTCCTGCCTGTTCC[A/G]AAGGCCCCTCTTCTT | 7464 |
rs573576107 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173861 | GTGGCTCACGCCTGT[A/C]ATCTCAGCACTTTGG | 7464 |
rs573586258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98163149 | CCCAACTCCCAGAAA[A/G]GATGTAGTCATCTCT | 7464 |
rs573735613 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171625 | GCCCCCGGGAGGATA[C/T]GACTGAGCTGAGCTT | 7464 |
rs573900863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98129721 | CCGCACTGAAGCCCT[A/G]ACCCTGATTCTCCCA | 7464 |
rs573916490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186596 | TCTGAAATTCTCCAT[G/T]ATCAAGTGTTTATAA | 7464 |
rs573925211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98161577 | TTAATAATAATTCTA[A/G]TAAATAAAGCAGGGG | 7464 |
rs573944877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136334 | AGACACTGTCCTTTA[C/T]GTTCCTCAGCATCTG | 7464 |
rs573952288 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193067 | CGGCCGGGTACAGTG[A/C]GCGCGCCGAGCCCGG | 7464 |
rs574027996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98128109 | CTCTCAATTGCTTGG[A/G]GCCACTGGGCACGCC | 7464 |
rs574050295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149588 | GGGATCAGGTGTGCC[A/G]CAGGCCACGGGGAGG | 7464 |
rs574064658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192293 | GCAGCGAGCCGTCGG[G/T]AGCCCGGACCTCGAG | 7464 |
rs574069092 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123651 | AGACGCTCACCACCA[C/T]GGCTGGCCAACTTTT | 7464 |
rs574122853 | in-del | -/AG | 0.00953873 | 0.0683987 | intron-variant | CORO2A | GRCh38.p7 | 9:98149215 | AACTTTTAATTAAAA[-/AG]AAAAAAGCAAAAATA | 7464 |
rs574190208 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98181039 | CACTGACTTTTTTTT[-/C]CACATCATCTGGCAA | 7464 |
rs574211124 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169740 | GAAGCAAAAAGAAAA[C/T]AAAAAAGCATCATTT | 7464 |
rs574271907 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121874 | AGAGCTCTGCTGCCC[C/T]GACAATGCCTGGGAT | 7464 |
rs574302185 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122591 | AGATTCACTAAGGAG[A/G]GACAAAGAAAAGCTT | 7464 |
rs574335567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98184045 | CTATAGATGACTTAA[A/C]GTATACAGGAGGGTG | 7464 |
rs574354970 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98147512 | TTCCATAATTATGAA[A/C]CTGAGCTAGATTAGA | 7464 |
rs574385574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98126197 | TACGCCACCACACCC[A/G]GCTAATTTTTGTATT | 7464 |
rs574392269 | in-del | -/TTG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152132 | CTTTTGCTGTTTTTT[-/TTG]TTTTTTGTTTTTTCT | 7464 |
rs574419131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98146920 | GGCCTGTCTGTGCAG[C/G]TAAGTGCTATGGCAT | 7464 |
rs574423681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190037 | TTACAGGCATGTGCC[A/G]CCACACCCAGCTAAT | 7464 |
rs574434661 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151847 | TTTGAGACGGAGTTT[C/T]GCTCTGTCGCCCAGG | 7464 |
rs574510073 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186040 | AACACACGCCTGCCC[C/G]TGCACTGCCTGTGGG | 7464 |
rs574511230 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98132019 | GGGTCTGGGCTCGCC[C/T]GGGGCTGTCAGCATC | 7464 |
rs574554092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98131508 | TTTTTTGCAGAGATG[A/G]GGGTCCTGCTGTGTA | 7464 |
rs574833966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98138829 | CGAGGCGGGTGGATC[A/G]CGAGGTCAGGAGATC | 7464 |
rs574881856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98138397 | GCCTGGGTGACAAGA[A/G]TGAAACTATGTCTCA | 7464 |
rs574951036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98157074 | GCTTGCTTACTGTTT[A/G]CCTCTCCTAGCTAGT | 7464 |
rs574980357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2A | GRCh38.p7 | 9:98188095 | ACTCTGTCCCAGCTC[A/G]TGCTTCTCTGAACAT | 7464 |
rs575018726 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194583 | GGTGCGTGCCACCAT[C/G]CCCAGCCAATTTTTA | 7464 |
rs575034430 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186956 | GCACCTGTCTTCGTC[C/T]GTTGCTGCAGCTACA | 7464 |
rs575064289 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137700 | CTGTCTGCAAGACAG[C/T]GCCCAGGAGGGTTGG | 7464 |
rs575094892 | in-del | -/TG | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120886 | AGGGCAAAGACTGTC[-/TG]TTCTGCCTGTTTTCC | 7464 |
rs575146399 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139336 | GTCTCTACAAAAAAT[A/C]AAAAAATTAGGCCTG | 7464 |
rs575157930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151653 | ATCCTAACACTTTCA[A/T]CTTTTCTTTCGCTAT | 7464 |
rs575212747 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98169044 | GAAGAAGCCCTTTGC[-/T]TTTTCTCCATCAGCA | 7464 |
rs575215161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98158605 | CTACTAGGAGAGTCT[A/G]GGCCACTGGGACCGA | 7464 |
rs575217395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151109 | ACCCTCCCTATTTAT[C/T]TGGATGAACAACCAT | 7464 |
rs575291908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142381 | GTACTTCCTGTGCTC[C/T]GAGGGAGCACCAGTG | 7464 |
rs575307313 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO2A | GRCh38.p7 | 9:98168509 | TTATATAACTTGCCT[A/G]AGATCACATAGCTAG | 7464 |
rs575343616 | snp | C/T | 4.99913e-05 | 0.00499931 | missense | CORO2A | GRCh38.p7 | 9:98134876 | ACCAGGCCTACTCTG[C/T]GCGCGTGGCCCACGA | 7464 |
rs575344128 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173880 | TCAGCACTTTGGGAG[A/G]CTGAGGCGGGCAGAT | 7464 |
rs575352760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98179306 | GTGACCCTGCAGGAC[A/G]CGGAGACCCTGCTGC | 7464 |
rs575456152 | in-del | -/T | 0.0349115 | 0.127424 | intron-variant | CORO2A | GRCh38.p7 | 9:98181335 | ATCTCTCTCTCTTGC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs575464323 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CORO2A | GRCh38.p7 | 9:98172075 | TGAGGAGGAGGGAGA[G/T]AATTCTGAGGCCTTC | 7464 |
rs575519476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190792 | GAGATGACAGGAGAC[C/T]CAGGTAGCACTTAAG | 7464 |
rs575534726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98176513 | CTGTTCCTGGAGCCC[C/T]GCCAGCCACATCCAT | 7464 |
rs575542189 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135665 | TCCTGGGATGCTGCT[C/G]ACTTGATCTTCCTTA | 7464 |
rs575571202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159006 | TCCTCTTGGCCAGAC[A/G]GACCCTTCTGAATAC | 7464 |
rs575571568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98178453 | TGTCCATTCTGTAAG[C/T]GCTAGTTAGCTTAGA | 7464 |
rs575653314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98155276 | GTCATGTTTATTATA[C/T]CCTTTTCCACTCTAT | 7464 |
rs575689838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98154799 | TTTTGTGGTTTTGTA[C/T]ATTCACTTGTATGGA | 7464 |
rs575693000 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120682 | AAGACTGGGGGACGT[A/G]CAGTTTACCCTGCTT | 7464 |
rs575799920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98130849 | CAGGGAAAGAGTGGC[C/T]AGCGAGGCCTGCCCA | 7464 |
rs575844265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127328 | TCCAGTACACCAGGA[A/G]GCCCGCTCAGCCACT | 7464 |
rs575844512 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174289 | AGCTGGGGTCCATGA[C/T]AGCACCTACCTTATA | 7464 |
rs575901806 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180559 | TTCATCTCCTTAAAA[G/T]AACCATCTCATCTCC | 7464 |
rs575916163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98183975 | TAAAAATATGTATAT[A/G]CAGTATAATAACTAG | 7464 |
rs575940208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140252 | CACAAATATTCCCGA[C/G]GTGCCCAGGGGACAG | 7464 |
rs575975387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98159214 | CAGGTACATGCCACC[A/G]TACCTGGCTAATTAA | 7464 |
rs576044648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98144342 | CCATTTACAAGTGCA[C/G]AGGCTGGGGCTCAGA | 7464 |
rs576083698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98151016 | GGCCAGACAGCTGCT[C/G]TCTGCATTGCTTCCT | 7464 |
rs576182299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO2A | GRCh38.p7 | 9:98163192 | GCACTGAGTTTATTT[C/T]TTTTTTTTTCTTTGA | 7464 |
rs576246720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98130485 | ACAAGTCCAAATCCC[A/G]CTCCTATCTGAGAGC | 7464 |
rs576287555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98137392 | AGGAGGGGTGGTGCC[A/G]CTAGTCCTACAGCAC | 7464 |
rs576325415 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123034 | AGTTTTCTCTTAGGT[A/C]AAGGTTTCAGGTGGC | 7464 |
rs576400024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98136467 | TGTTGCCCATTTTGC[C/G]TTGGCTGCCAGGTAG | 7464 |
rs576402834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187267 | CACCCTGGGCGACAG[A/G]GCAAGACTCCATCTC | 7464 |
rs576431814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98181121 | GTGGACAATAACCAG[C/T]CCTGGGAAGGAGGCC | 7464 |
rs576433982 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122450 | CTCCAGAATCTAATC[C/G]CCCTGTGCAATGGAG | 7464 |
rs576447518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98140929 | AATCTAAACAAGAAC[A/G]GTAGATTACAGTATT | 7464 |
rs576481540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98140355 | GGATTTTTTCTAGAG[A/G]GACTTTCAAGAACAG | 7464 |
rs576481651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148121 | AAAAAGAGGCCAGGC[A/G]AGGTGGTTCATGTCT | 7464 |
rs576689958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148858 | AACCCAGCTGAACTG[C/T]GAGAGAAATACAGTG | 7464 |
rs576693679 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129623 | CTTTGTGCTGTTGCA[A/C]ACGTCAAGTACAGCC | 7464 |
rs576775544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98133379 | TGATGTGCAGGCTGA[A/C]GCTGCTTGTGGCAGG | 7464 |
rs576818159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168871 | ATGGGGAAACAGACA[C/T]ACACATGCAGAAGGC | 7464 |
rs576828953 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178914 | ACAAGAACCTGAGAA[A/G]GGATGTGACTTGTCC | 7464 |
rs576844124 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98184237 | ATTTTATTTTATTTT[A/T]TTTTTTAATAGAGGC | 7464 |
rs576915429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98125432 | ACATTCAGTCTCTGG[A/G]TCTAAGACCCTAAAT | 7464 |
rs576947398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153611 | ATGGGGTCTTGCTAT[A/G]CTGCCCAGGCTATAT | 7464 |
rs576992848 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO2A | GRCh38.p7 | 9:98190672 | ATTAGCAATTAAAGT[A/C]ATAGCATGACTTTTT | 7464 |
rs577027929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98153122 | TTTGTTATTTTGAGA[C/T]GGAGTTTTGCTCTGT | 7464 |
rs577079421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98190134 | AGGTGATCCGCCCAC[C/G]TTGGCCTCCTAAAGT | 7464 |
rs577084602 | snp | A/G | 0.000120824 | 0.00777158 | missense | CORO2A | GRCh38.p7 | 9:98124887 | TCTCCTCCTGTTGCC[A/G]GTAGAACATCTGCAG | 7464 |
rs577219857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98165883 | TCAGGTATTCTGGGG[G/T]TGGGGCTCACCACTC | 7464 |
rs577258600 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160838 | ATCACTGCCTCCTAT[-/G]ACCCGTTAGCCAGTG | 7464 |
rs577260737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98132469 | CCACCTGGATCCCTC[C/T]CATCCACATGGAGTC | 7464 |
rs577350060 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190355 | CCACAGGCGAATCCC[C/T]ATAGCCTTGCCAGCA | 7464 |
rs577507796 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160706 | CTCCTCCCTCACCTT[A/G]AGCAACTGCTGGGGG | 7464 |
rs577567340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98145886 | CCCAGCTGATTTTTT[A/G]TTTTTGGTAGAGACA | 7464 |
rs577570567 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123108 | GATGAAGAAACTGAG[A/G]CCAGAGAGGGCAGGA | 7464 |
rs577581296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98192190 | CCGGGCCACAGCAGG[A/G]GCCTGTCGGGACCGG | 7464 |
rs577584473 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131723 | TCAGAGAGAAAATGT[G/T]ATTTGTCCAGTCTTT | 7464 |
rs577620110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98191428 | AAACTGCTGGGCCTG[A/G]GGCTGCTGGGTCTGG | 7464 |
rs577620719 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134706 | AACACCTTGATTTTC[A/G]ATTTCTGGTCTCCAG | 7464 |
rs577652332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98152026 | TTCACCATGTTGGCC[A/G]GGCTGCTCTCAAACT | 7464 |
rs577654278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98145245 | TCCTACTTTCAGACC[C/T]TGTGAATTTGGAGAA | 7464 |
rs577679161 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174229 | CAAGGCAAGCATTTG[A/G]GTAGCTTTCCTAAAC | 7464 |
rs577696425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98128981 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCACA | 7464 |
rs577719594 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173916 | GAGATCGGGAGTTCG[A/G]GACTAGCCTGACCAA | 7464 |
rs577739653 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98168899 | GGCTAGCTGACAATT[A/C]CTACTGATCAAAAAG | 7464 |
rs577777793 | in-del | -/ACA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138448 | GGTTCACCAATGTTC[-/ACA]ACAATATTCTTCATA | 7464 |
rs577808008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98180039 | AACAGCAAGCAAAAA[A/C]AACTGCCTCAAAGTC | 7464 |
rs577815783 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98167911 | ACTGAAAGTGGGTGA[A/C/G]GGTACAAGAGGATTC | 7464 |
rs577825194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98168557 | ATCTGAAGCCAGGCT[G/T]TTCAGTCACAGGTCC | 7464 |
rs577852608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98166996 | GTAGTCCCAGCTACT[C/T]GGGAGGTCAAGGTGG | 7464 |
rs577880473 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171952 | AGTCAGGACATTGAG[A/C]CTGGGAAACGATTTC | 7464 |
rs577899199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98149515 | AAGAAGCCTGGCACC[A/G]GCATCTGCTTCTGGT | 7464 |
rs577925304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2A | GRCh38.p7 | 9:98135602 | GGGGCTGCCATGGCA[C/G]AGAGTAAGCTCCCTG | 7464 |
rs577944628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98148961 | AGTATAGAAATGGAG[A/G]GCAGGTTAATTGTCA | 7464 |
rs577961114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98142430 | GCCCTGGCCTCCTTC[C/G]TGCACACAGCCTTTC | 7464 |
rs577967581 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168328 | CTGGGCAAGTTACTT[A/G]ATGTGTCTATTTCCT | 7464 |
rs578020977 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175702 | CACAGTGGCTACTGA[C/T]ATGGTAGGGAACCTG | 7464 |
rs578028372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98141997 | TATATCTAGATGGTG[A/G]AATAAATGGCTGGCT | 7464 |
rs578187651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98127336 | ACCAGGAGGCCCGCT[C/T]AGCCACTGGGGTGGG | 7464 |
rs578202829 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139171 | TAATGAGTGAGGGGT[A/G]TCTTTTTGGAGTGAC | 7464 |
rs578213705 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172784 | CAGGCTGGGCCTGCA[A/G]GCCAGAAAGGCAGGA | 7464 |
rs578219822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2A | GRCh38.p7 | 9:98134218 | CACTTTCCCAGGCTA[C/T]AGTGCAGGTCAGAGA | 7464 |
rs578260259 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127320 | GAGGCTCTTCCAGTA[C/T]ACCAGGAGGCCCGCT | 7464 |
rs745324794 | snp | C/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193824 | TAGTCCACTGTACCA[C/G]CCCCCTGCCCAGAGC | 7464 |
rs745355788 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174815 | ATTAAACCTCTTTCC[-/T]TTATAAATTACCCAG | 7464 |
rs745375663 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183075 | GCATTCACCCTGGAT[C/T]TCCAGAGCTTCACGG | 7464 |
rs745377543 | snp | A/G | 8.23852e-05 | 0.00641762 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129795 | TGTCCCTCACTTACC[A/G]ATCCCCTTCTGTGGG | 7464 |
rs745390758 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194614 | TATTTTTTGTAGAGA[C/T]AGGGTTTCGCCACGT | 7464 |
rs745399135 | snp | C/T | 3.2956e-05 | 0.00405918 | missense | CORO2A | GRCh38.p7 | 9:98128630 | GCACAATCATGGAGA[C/T]GGGCTCGATGAGGCT | 7464 |
rs745456459 | snp | C/G | 1.67203e-05 | 0.00289134 | intron-variant | CORO2A | GRCh38.p7 | 9:98128558 | CTGGGTCTGTCTTCT[C/G]CAGGACAGGTTCCCC | 7464 |
rs745467151 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166956 | AAATAAAAAAAAAAT[C/T]AGCTGGGCATGGTGG | 7464 |
rs745494360 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139931 | GACATACAGGTCCCC[C/T]AGCCCATGCCACACA | 7464 |
rs745573417 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167933 | AGAGGATTCATTTGA[A/C]TCTTTCCTTTAATTT | 7464 |
rs745654180 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133113 | GGCCAACAGGCTGCC[A/G]TTGGTGTTGAAGGAC | 7464 |
rs745657766 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152652 | AATAAGTCAAGTTAA[C/T]AGCATGAATAATGTG | 7464 |
rs745691845 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152821 | TACTGAACAACTGAC[C/T]TTTACTCCTGAAAAA | 7464 |
rs745703254 | snp | A/G | 3.30017e-05 | 0.00406199 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133047 | ACTGACCTGGAGGAC[A/G]GTCCCTGCTCGGGGG | 7464 |
rs745744306 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161681 | GGCAATGGTCACCCG[C/G]GCTGGAGTAGGGCAG | 7464 |
rs745806635 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121230 | GCACAATTATTGTAG[C/T]GTTAAGGTGGATACC | 7464 |
rs745828258 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169341 | GAGGGAGTGCCTCCT[-/C]CCCCACATCTGACAC | 7464 |
rs745927211 | snp | C/T | 1.6563e-05 | 0.00287771 | missense | CORO2A | GRCh38.p7 | 9:98134895 | CGTGGCCCACGAGTT[C/T]CTTCCTGTAGGCCGT | 7464 |
rs745941899 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143173 | CCTGGAGAGGCATCA[A/C]CTCCAAGTCTCCAAG | 7464 |
rs745945650 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190947 | AGGTCATAGGCACTA[C/T]TTCAGCCCTAGAATT | 7464 |
rs745992793 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169214 | TCCCCGCCCCCGCGC[C/T]GCCCATCCTTCTGGT | 7464 |
rs746005092 | snp | A/G | 1.72282e-05 | 0.00293492 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134836 | AGCACTGAAGAGGAT[A/G]TTGGCGGCCGTGGGG | 7464 |
rs746087766 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189456 | TTTTGAAATAGCAAA[G/T]GTTTAAGGCTGAAAC | 7464 |
rs746151802 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129021 | CACCGCAGTCTCACA[C/T]TCCTGGGCTCAAGCG | 7464 |
rs746170770 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155050 | TCAGAAGTGTCTGAT[C/T]GTTTACACAACTCTG | 7464 |
rs746241278 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158543 | GAGTTTGGAAACAGT[A/G]GGCCTGAGCCCAGCC | 7464 |
rs746257617 | in-del | -/CACACACACACT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153683 | ACACACACACACACA[-/CACACACACACT]CACACACACACCCCG | 7464 |
rs746259993 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123758 | CCTCCCAGGCTCAAG[C/T]GATTCTCCTGCCTCA | 7464 |
rs746283600 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | CORO2A | GRCh38.p7 | 9:98126701 | CTTCTGCAGCCAGCT[C/T]TTCTGTCTGATTCAA | 7464 |
rs746322664 | snp | A/G | 7.59042e-05 | 0.00616006 | intron-variant | CORO2A | GRCh38.p7 | 9:98157372 | GTAATGGGCAGGGCT[A/G]GGACTTTCTAGAAAC | 7464 |
rs746363406 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172911 | AAGGCACTTCTGCCC[A/G]CAAGACTGGCTGTGA | 7464 |
rs746395568 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134403 | CAGGGTTCCCCCCAA[A/G]ACTCATGTCCACCTG | 7464 |
rs746396757 | in-del | -/CACACT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153689 | ACACACACACACACA[-/CACACT]CACACACACACCCCG | 7464 |
rs746414757 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173729 | GGGCTTCAGAGTCAG[A/G]GAAACCTGGATCCAA | 7464 |
rs746516797 | snp | A/G | 1.65247e-05 | 0.00287438 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132196 | TCACCTGGTCCCACA[A/G]GGCCACCTGCCGGTT | 7464 |
rs746542448 | snp | G/T | 1.9999e-05 | 0.00316214 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124755 | TGTCCCTGAGGGTGA[G/T]GAGGGCAGAGGTCTC | 7464 |
rs746571859 | snp | C/G | 2.37256e-05 | 0.00344416 | intron-variant | CORO2A | GRCh38.p7 | 9:98157402 | CCCAGGCTCTTTCCA[C/G]TTTCCCTCTGTCCTG | 7464 |
rs746697292 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131332 | CCTTAACAAATCACT[-/T]TTTTTTTTTTTTTGA | 7464 |
rs746705526 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186034 | CCAGGGAACACACGC[C/T]TGCCCCTGCACTGCC | 7464 |
rs746724593 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164723 | AGTGATACAGTGGGA[C/T]CCAGTGTGCTAGGAC | 7464 |
rs746758370 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128570 | TCTCCAGGACAGGTT[C/T]CCCACCTGCCTCCCA | 7464 |
rs746789995 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128637 | CATGGAGATGGGCTC[A/G]ATGAGGCTTTTGGTT | 7464 |
rs746825564 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168027 | GGTGGCCCAGGCCCC[A/G]GAGCTTGACTGTCAG | 7464 |
rs746863742 | snp | A/C | 6.61343e-05 | 0.00575002 | missense | CORO2A | GRCh38.p7 | 9:98133217 | GGTTCCAGATCATCA[A/C]CTGCATGGCAGAGAG | 7464 |
rs746864662 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177945 | GTCAGACTTATTAGC[-/T]TTGTCACTGTTTTTG | 7464 |
rs746870800 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | CORO2A | GRCh38.p7 | 9:98133120 | AGGCTGCCGTTGGTG[C/T]TGAAGGACATGGAGA | 7464 |
rs746983577 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140325 | GTCCTTGACTTTGCA[A/G]AATCAATAGTCTTGG | 7464 |
rs746984673 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178771 | TTTTTTCCTGCACCC[C/G]AATGTGCATCTTGCA | 7464 |
rs747008269 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153908 | TGAGTTTTTCTCATG[G/T]CTGGGTATTGGGCTT | 7464 |
rs747042928 | snp | C/T | 2.33261e-05 | 0.00341504 | intron-variant | CORO2A | GRCh38.p7 | 9:98130914 | TGTCTGCCGCTGTCT[C/T]AGGGGTCCAGGAGGT | 7464 |
rs747076180 | snp | A/G | 1.74519e-05 | 0.00295392 | intron-variant | CORO2A | GRCh38.p7 | 9:98124909 | CATCTGCAGCAACTG[A/G]GGAAGAAAGATCGGA | 7464 |
rs747077569 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171885 | ATCAAAGTGTGTAAC[C/T]GGGGGTGTGACATGG | 7464 |
rs747099970 | snp | A/C | 1.68363e-05 | 0.00290136 | intron-variant | CORO2A | GRCh38.p7 | 9:98133262 | AGGGGCCACCTTGCC[A/C]CTGGGCCTCATAGTT | 7464 |
rs747144365 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160925 | TGTGACCCTCTAGGA[C/T]TCTCGTCCTTGGCCA | 7464 |
rs747237868 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144951 | GGGTGAGATGTGGGA[C/T]CAGGGACCGCCCAGA | 7464 |
rs747274134 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170742 | GCCACTGAGCCTGGC[C/T]GAGAATCCTAATTCT | 7464 |
rs747310480 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165434 | GTGAAGAGGATTTCA[C/T]TCAATCTCCAATCTT | 7464 |
rs747336197 | in-del | -/GACACGTGCGGTCGGTATTGGAGA | 0.000115841 | 0.00760968 | intron-variant | CORO2A | GRCh38.p7 | 9:98132308 | CTGGCCTCCTGGAGG[-/GACACGTGCGGTCGGTATTGGAGA]GACACGTGCGGTCGG | 7464 |
rs747337053 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190246 | CTAGTTACTTCCTTA[A/G]GATAAAGTCCCCAAA | 7464 |
rs747346454 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155261 | AGAAATGAGTCTTTT[C/G]TCATGTTTATTATAT | 7464 |
rs747348070 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155342 | ATTTTTATTGCTCAA[-/T]TTTTTTTTTTTTTTT | 7464 |
rs747364299 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125535 | TGACTTCCAGGGCTG[C/T]TGAGAGAATTCAATC | 7464 |
rs747367794 | snp | A/G | 5.87769e-05 | 0.00542079 | intron-variant | CORO2A | GRCh38.p7 | 9:98126951 | GCAACATGTGTGGGA[A/G]ATACAGCTACCTGTG | 7464 |
rs747401593 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134047 | GTGAGCCACCATGTC[C/T]GGCCCCCCACCTCCC | 7464 |
rs747455545 | snp | C/T | 1.65381e-05 | 0.00287555 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132287 | GCTGGCCCGGTGCCC[C/T]TTGTAGCTGGCCTCC | 7464 |
rs747487420 | snp | A/G | 1.6593e-05 | 0.00288031 | intron-variant | CORO2A | GRCh38.p7 | 9:98126827 | CCAGGATTGGGTCTG[A/G]AAGGGAAGCAGAGCC | 7464 |
rs747489903 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160339 | GAGATCACCTGAAAC[A/G]CAGGAGGAGTTAAGC | 7464 |
rs747501901 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151815 | ACCATGCCCGGCTAA[-/TT]TTTTTTTTTTTTTTT | 7464 |
rs747521577 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137021 | TAAGCCATACCACCA[C/T]ATTTTAGAAGTGGGT | 7464 |
rs747531801 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123915 | CCAGCTTGGCCTCCC[A/G]AAGTTCTGGGATTAT | 7464 |
rs747588453 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137351 | TTATGCCCATTTTAT[A/G]TGGGGGGGAACTAAG | 7464 |
rs747611933 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164883 | GGCAGGACTTACAGC[A/G]CTAAACTGGGGGAAG | 7464 |
rs747647298 | snp | A/G | 0.000147525 | 0.00858725 | intron-variant | CORO2A | GRCh38.p7 | 9:98126985 | AGGCCCAAACCCACA[A/G]AGCAGGGCTAACAGA | 7464 |
rs747647609 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165020 | GCTACCCAGGCTGGA[A/G]TGCAGAGGCGTGATC | 7464 |
rs747652030 | snp | A/G | 3.31148e-05 | 0.00406894 | intron-variant | CORO2A | GRCh38.p7 | 9:98132316 | CCTGGAGGGACACGT[A/G]CGGTCGGTATTGGAG | 7464 |
rs747726293 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192470 | CATCCCTCCCTCTCC[A/G]GGAGCTGCAGCCGCA | 7464 |
rs747839679 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174805 | CTGTGAGTCAATTAA[A/G]CCTCTTTCCTTTATA | 7464 |
rs747842285 | snp | A/G | 1.73039e-05 | 0.00294137 | intron-variant | CORO2A | GRCh38.p7 | 9:98157440 | TCCAGAGAGCTGTTT[A/G]GGCCTGGGGGTGTCC | 7464 |
rs747905973 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145458 | ATGAACAAACCCCTA[C/G]AACTGGAAGAGACTT | 7464 |
rs747906125 | in-del | -/AAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188789 | AACAACAACAACAAC[-/AAAA]AACAACAACAAAAAC | 7464 |
rs747938637 | snp | A/G | 3.66247e-05 | 0.00427913 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98131021 | CACGCCCGAGGAGCC[A/G]TCCAGGTCCTCCTCC | 7464 |
rs747955238 | snp | A/C | 1.98829e-05 | 0.00315294 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124773 | GGGCAGAGGTCTCTG[A/C]TCAGAGCTGCTCTGA | 7464 |
rs747964121 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160089 | TTGCAGGGGCTTGTG[C/T]ATCCCATAAAGCTCA | 7464 |
rs747978763 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | CORO2A | GRCh38.p7 | 9:98128671 | ATCAGCTTGTAGAAG[C/T]GGAAGATCTCGCAGG | 7464 |
rs748006683 | snp | C/T | 1.65002e-05 | 0.00287225 | intron-variant | CORO2A | GRCh38.p7 | 9:98129748 | CCCACCTCGGCCTCC[C/T]GAAGTGCTGGGATTA | 7464 |
rs748025218 | snp | G/T | 1.82042e-05 | 0.00301691 | missense | CORO2A | GRCh38.p7 | 9:98134816 | CTCACCTTGTAGTCA[G/T]AGCCAGCACTGAAGA | 7464 |
rs748098357 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142950 | ACAGGCAGGAGCGGA[C/T]ATTAGCCAGCCTGGT | 7464 |
rs748098565 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130125 | AGGGTCTCACTTTAT[G/T]GCCCAGGCTGGAGAG | 7464 |
rs748104776 | snp | A/G | | | missense | CORO2A | GRCh38.p7 | 9:98128236 | CTGCTGTTGGAGGGT[A/G]TATGTCCTCTTGGTA | 7464 |
rs748113571 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126196 | GTACGCCACCACACC[C/T]GGCTAATTTTTGTAT | 7464 |
rs748158513 | snp | A/T | 1.64727e-05 | 0.00286986 | missense | CORO2A | GRCh38.p7 | 9:98126650 | CTGCCCACCTTGGCA[A/T]CTTCTCCTCCAACAG | 7464 |
rs748243760 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121473 | AAATTACCTATCCCT[C/G]TCCCTTGCTGTGAAA | 7464 |
rs748243954 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122252 | CTTCCATCTTCACTG[C/T]ACTGCAGATCACCTG | 7464 |
rs748256870 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171488 | GACAGCGTCACTTAT[C/G]GGGGAGCTCAGAGGA | 7464 |
rs748260017 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187143 | ACAAAATTAGCCGGG[C/T]GTGGTGGTGGGCGCC | 7464 |
rs748317479 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146413 | AACAGGCAAGAGGGA[A/G]GGACCCTGCCTGCAG | 7464 |
rs748326645 | snp | C/G | 2.25558e-05 | 0.00335818 | intron-variant | CORO2A | GRCh38.p7 | 9:98130925 | GTCTCAGGGGTCCAG[C/G]AGGTCACCTCCCTCC | 7464 |
rs748341713 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182732 | GAGGACAAGACTATC[C/T]AGCTACAATGCGATG | 7464 |
rs748406527 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157358 | AGGTCACACAGCTAG[C/T]AATGGGCAGGGCTAG | 7464 |
rs748520985 | snp | A/T | 1.65217e-05 | 0.00287412 | intron-variant | CORO2A | GRCh38.p7 | 9:98137547 | CTCTTCAGGAAGGGG[A/T]AGCCCCTCAGGGGCT | 7464 |
rs748521550 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167103 | AGCAAGATCCTGTCT[-/C]AAAAAAAAAAAAAAA | 7464 |
rs748574075 | snp | G/T | 1.65405e-05 | 0.00287576 | missense | CORO2A | GRCh38.p7 | 9:98134916 | TGTAGGCCGTGAGGT[G/T]CCTGGTCAGCAGCTG | 7464 |
rs748623206 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125868 | GACTACAGGCACGCA[A/C]CACCATACCCAGCTA | 7464 |
rs748635756 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165494 | CGCCAAGCCGTGTCA[A/G]GAGCAGGGCTCGGAG | 7464 |
rs748644425 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138290 | CGTGGTAGCATGCAC[C/T]TGTAATCCCAGCTAC | 7464 |
rs748644824 | in-del | -/GGGAAGGCC | 2.96837e-05 | 0.0038524 | intron-variant | CORO2A | GRCh38.p7 | 9:98131079 | GGGGAAGGGGAGGCA[-/GGGAAGGCC]GGGAAGGCCTGGGTC | 7464 |
rs748648881 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190413 | TTGCTAATTTTACAG[A/G]AATAAATACAGACTG | 7464 |
rs748663334 | in-del | -/C | 3.4241e-05 | 0.00413755 | intron-variant | CORO2A | GRCh38.p7 | 9:98126531 | CATGTGAAAGGCCCA[-/C]CCCGTCCTCCTTCAC | 7464 |
rs748716249 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187458 | GGCGAAACTCCATCT[-/CA]AAAAAAAAAAAAAAA | 7464 |
rs748781900 | snp | A/G | 1.65146e-05 | 0.0028735 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128198 | GCTGAGCCACTCCTG[A/G]GCCGTCAGGGAGGGC | 7464 |
rs748815887 | snp | A/G | 1.6788e-05 | 0.00289719 | intron-variant | CORO2A | GRCh38.p7 | 9:98128302 | AGGGTGGTAGGGTAG[A/G]CTGCTCAGATGGGAA | 7464 |
rs748831616 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166807 | GATCAGTAAAATGTG[A/G]TATATTCAAACCATG | 7464 |
rs748837167 | snp | C/G | 1.65559e-05 | 0.00287709 | intron-variant | CORO2A | GRCh38.p7 | 9:98133035 | CCCTGGCCCAGAACT[C/G]ACCTGGAGGACGGTC | 7464 |
rs748862218 | in-del | -/TTAAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168115 | GCTTCTAAATTAAAG[-/TTAAAA]TTAAATAAAGTGTAA | 7464 |
rs748872959 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128316 | GGCTGCTCAGATGGG[A/C]AAGGCCCTTAGACCT | 7464 |
rs748888036 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137401 | GGTGCCGCTAGTCCT[A/G]CAGCACCAAGAATGT | 7464 |
rs748913791 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153407 | CATCCGGCTGATAAC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs748970000 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149557 | GGGAGCTTCCAATCA[C/T]GCAGACAGTGAAGGG | 7464 |
rs749051197 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150484 | TCCCTTTAGAGCCTC[A/G]AGTGGCTCTCGGCTC | 7464 |
rs749078665 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161508 | GCAGCGAGCCAAGAT[C/T]GCACCACTGCACTCC | 7464 |
rs749113336 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185707 | CCAGTTATTGAGCAC[A/G]CCATAGACCACGCCC | 7464 |
rs749144435 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135786 | TCAATTCAGCAAATA[-/TT]TATTTCCTGGTCATC | 7464 |
rs749197411 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190790 | CGAGATGACAGGAGA[-/C]CCCAGGTAGCACTTA | 7464 |
rs749202277 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131115 | TGGGGGCCCTCAGTG[A/G]TGCTCCCGGAGATAA | 7464 |
rs749241937 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160856 | CCGTTAGCCAGTGGA[C/T]CATGGGAGGCAGTGA | 7464 |
rs749285367 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188694 | ACTTGAACCCAGGAG[G/T]CAGAGGCGGAGGTTG | 7464 |
rs749334038 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189298 | TGATTGCAAAGCACG[C/T]CCAATCTGTTCTGAA | 7464 |
rs749366620 | snp | A/G | 1.65622e-05 | 0.00287764 | intron-variant | CORO2A | GRCh38.p7 | 9:98133225 | ATCATCACCTGCATG[A/G]CAGAGAGCCAGCTCT | 7464 |
rs749368868 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123692 | ACGGAGTCTCACTCT[A/G]TCACCCAGGCTGGAG | 7464 |
rs749409257 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | CORO2A | GRCh38.p7 | 9:98126781 | GGCAGTGGGTGGGGT[C/T]TCAGCAGCTCAGAGC | 7464 |
rs749492230 | in-del | -/G | 1.68199e-05 | 0.00289994 | intron-variant | CORO2A | GRCh38.p7 | 9:98128737 | GAAGGCAGACAGGGA[-/G]GGCCAAGAGGTTCTG | 7464 |
rs749527165 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153072 | AAGTACAGTATTTGG[G/T]GGTAAAGGGTCATCT | 7464 |
rs749571266 | in-del | -/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121523 | TAGATGTAAAAATAA[-/T]AATACAAAAAAGTTT | 7464 |
rs749579948 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163432 | TGACCTCAGGTGATC[C/T]GCCTACCTTGGCCTC | 7464 |
rs749589049 | snp | A/C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155441 | AACCTCTGCCTCCTG[A/C/T]GTTCAAGCAATTCTC | 7464 |
rs749639686 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133505 | CCAGCTAATCCAGGC[A/G]GTTTCAGTTATTAGC | 7464 |
rs749659304 | snp | C/T | 8.83322e-05 | 0.00664517 | missense | CORO2A | GRCh38.p7 | 9:98131008 | AGAAGGGAAACAGCA[C/T]GCCCGAGGAGCCGTC | 7464 |
rs749758482 | snp | A/C | 1.65179e-05 | 0.00287379 | intron-variant | CORO2A | GRCh38.p7 | 9:98137550 | TTCAGGAAGGGGAAG[A/C]CCCTCAGGGGCTGAC | 7464 |
rs749830349 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143141 | GACCCCACAGAACCC[-/T]GGCTTGGGCCGCCCT | 7464 |
rs749846242 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182849 | TTAACATCTCTGAAA[C/G]TGGGATGCAACTTAC | 7464 |
rs749909783 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180333 | ACCGGCTGCTACAAG[A/G]CTCAGCTTAGAGAAG | 7464 |
rs749929107 | snp | A/G | 3.35711e-05 | 0.00409688 | intron-variant | CORO2A | GRCh38.p7 | 9:98128734 | CCTGAAGGCAGACAG[A/G]GAGGGCCAAGAGGTT | 7464 |
rs749963412 | in-del | -/CAA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187458 | GGCGAAACTCCATCT[-/CAA]AAAAAAAAAAAAAAA | 7464 |
rs749982634 | snp | A/G | 2.75683e-05 | 0.0037126 | intron-variant | CORO2A | GRCh38.p7 | 9:98134761 | TGTATTCCAGTTTGT[A/G]GGAACTTGTTGGGGC | 7464 |
rs750057758 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141601 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTTCCAAA | 7464 |
rs750064376 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164185 | TAGAACCACAAGTTA[C/T]CCAGTTATTTCAAAA | 7464 |
rs750091425 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154695 | TAAGGTTAATTAAAT[A/G]ATATAGTTTAAAATT | 7464 |
rs750179873 | snp | C/T | 1.71926e-05 | 0.0029319 | missense | CORO2A | GRCh38.p7 | 9:98134838 | CACTGAAGAGGATGT[C/T]GGCGGCCGTGGGGTG | 7464 |
rs750210573 | snp | A/G | 3.1453e-05 | 0.00396554 | intron-variant | CORO2A | GRCh38.p7 | 9:98131081 | GGGAAGGGGAGGCAG[A/G]GAAGGCCTGGGTCAC | 7464 |
rs750225488 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163096 | TGCAGGCTTGGTGGG[C/G]CTGATGCCATGGGAT | 7464 |
rs750243854 | snp | C/T | 1.64727e-05 | 0.00286986 | stop-gained | CORO2A | GRCh38.p7 | 9:98126639 | CCTGTGTTCTGCTGC[C/T]CACCTTGGCATCTTC | 7464 |
rs750245901 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188123 | CATGCCAGGCATGGT[C/T]CTGCCTCAGGGCTTT | 7464 |
rs750304084 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183341 | CCTTCAGAAACCCCC[A/C]CAGACATCTCCTCCA | 7464 |
rs750317261 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147248 | AGGAATCAGGTGACA[C/T]AAGAGTTATTATTAA | 7464 |
rs750385796 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134102 | AGGTGTCTCTGTAAA[A/C]CCCTATAGTGTCAAA | 7464 |
rs750440117 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173326 | TGATTCACAACTATC[C/G]CTCAGTTTACCCCTC | 7464 |
rs750447688 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156163 | TCTGACCTCAGCCTC[C/T]TAAGTAGCTAGGACC | 7464 |
rs750468185 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166273 | AACCTTAGAAGAAAA[C/T]GAAGAGCAAAATCTT | 7464 |
rs750489715 | snp | G/T | 8.2837e-05 | 0.00643519 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128171 | TCTGCCTTCCTCACC[G/T]CGATTCATCCCGCTG | 7464 |
rs750543089 | snp | A/G | 8.3309e-05 | 0.00645349 | intron-variant | CORO2A | GRCh38.p7 | 9:98132347 | AGACAGTAGAGGATC[A/G]GGGGCAGCTGGGGTT | 7464 |
rs750668651 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176209 | GAAAGCCTTGTGCCC[C/G]TTATCAACCCATGAG | 7464 |
rs750697854 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138065 | TGGCAGTTCCTCAAA[A/G]GGTTAACCGGTTCCC | 7464 |
rs750786716 | snp | A/G | 1.65269e-05 | 0.00287457 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132265 | GGTTCCCCAGAAACA[A/G]CACTTTGCTGGCCCG | 7464 |
rs750817514 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124837 | CTGTTTGGCCTGGAC[C/T]TCTCGCTGGGTCAAC | 7464 |
rs750819300 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185274 | TGGGCCCTCACGGCT[A/G]TGATGGGTCTAGCTT | 7464 |
rs750859127 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136653 | GAAGTCTTGCTCTGC[C/T]TCCCACAGGCTGTGT | 7464 |
rs750859588 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150634 | GTACCCATTTACACC[G/T]AGCAGTTCATGCAAG | 7464 |
rs750909089 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147093 | GCAACATAGTGAGAC[C/G]CCATCTCTACTTACA | 7464 |
rs750932353 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184661 | CCTCATCCTCAGAGT[A/G]GGGCTGTGATCTGTG | 7464 |
rs750955249 | snp | G/T | 2.01457e-05 | 0.00317371 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124741 | ATGGAGCCGAGTGGT[G/T]TCCCTGAGGGTGAGG | 7464 |
rs751014005 | in-del | -/A | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193112 | TTTCCCCGAGCAGTT[-/A]ACAGCGGTTACCGAG | 7464 |
rs751084669 | snp | C/T | 1.65121e-05 | 0.00287329 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124852 | CTCTCGCTGGGTCAA[C/T]AGCTCCCGGAGCCTT | 7464 |
rs751131380 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142628 | CTCGGGCTGACGGGA[G/T]GCAAAGTGCCCAGGA | 7464 |
rs751142183 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167359 | TTTCAGTTTTGCAAG[A/T]TAAAGAGTTCTAGAG | 7464 |
rs751158561 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180536 | CCATGGCCTCTCTGA[A/G]CCTCAGTTTCATCTC | 7464 |
rs751191962 | in-del | -/GT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163713 | ACATACATGCGGGGT[-/GT]GTGTGTGTGTGTGTG | 7464 |
rs751234762 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143958 | CATGTCTGTAATTCC[A/T]GCACTTTGGAAGTCC | 7464 |
rs751237209 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134325 | CAGTGGAGCAGGGTC[-/G]GGGGGAACGATTTTC | 7464 |
rs751259744 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127658 | TCTCTACTAAAAATA[C/T]GAAAAATTAGCTGGG | 7464 |
rs751314792 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159296 | TCAAGCAATTCTCCT[A/G]TAGCTGCCTCTCAAA | 7464 |
rs751327304 | snp | A/G | 0.000103397 | 0.00718941 | intron-variant | CORO2A | GRCh38.p7 | 9:98126864 | GGACGGGGTGCCCAC[A/G]GGAAGATGGGCATAT | 7464 |
rs751350445 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152199 | GAGGACTATTCAGGC[-/T]TTTCTGTTTCTACTT | 7464 |
rs751373161 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154871 | TTCCCAGTTTTGCAA[C/T]AATACAAACAATGCT | 7464 |
rs751432213 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178806 | TCACTTTGGAGGCAA[C/T]TGGGATAGAAGATGA | 7464 |
rs751439267 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140443 | AGACCACTGTACTTG[-/T]TTTTTTTTTTTTTAA | 7464 |
rs751448430 | in-del | -/A | 1.67643e-05 | 0.00289515 | intron-variant | CORO2A | GRCh38.p7 | 9:98128299 | GGAGGGTGGTAGGGT[-/A]AGGCTGCTCAGATGG | 7464 |
rs751449606 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174281 | AAGCTGTAAGCTGGG[C/G]TCCATGATAGCACCT | 7464 |
rs751516719 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136304 | TGATTGTCCCTTTGG[C/T]GAAATCACCTCGGCA | 7464 |
rs751522159 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175159 | GGGGGTGGGGTGCGG[A/G]ATGGCCCTCCCTGTC | 7464 |
rs751577600 | in-del | -/GA | 1.65444e-05 | 0.00287609 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98134921 | CCGTGAGGTTCCTGG[-/GA]TCAGCAGCTGCTTGG | 7464 |
rs751583025 | snp | G/T | 1.64958e-05 | 0.00287187 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126771 | TCTCTCTGCAGGCAG[G/T]GGGTGGGGTCTCAGC | 7464 |
rs751609880 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182638 | ACCAGGTTCAAAGCC[C/T]AGCTTTGCCTCTTGC | 7464 |
rs751612958 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158299 | AAAAAAATAAAAGAG[A/G]GAGAGATTGAAAAAA | 7464 |
rs751616746 | snp | A/G | 1.65206e-05 | 0.00287403 | missense | CORO2A | GRCh38.p7 | 9:98132225 | TTGTTCCATCGGGAT[A/G]TGCCTGTGGACATCA | 7464 |
rs751628597 | snp | C/T | 3.44442e-05 | 0.00414981 | intron-variant | CORO2A | GRCh38.p7 | 9:98135007 | AGGGCACCTTGGCAC[C/T]GTCACCAGCCTAAGC | 7464 |
rs751646499 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137632 | GTTCCACTTGACATC[C/T]AAAACGTTGCCTCTG | 7464 |
rs751682929 | snp | A/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194165 | TGGTGGCATGTGCCT[A/T]TAGTTCCAGCTACTT | 7464 |
rs751769306 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193118 | CCGAGCAGTTACAGC[A/G]GTTACCGAGGCTTCC | 7464 |
rs751770663 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141516 | TGCCACCACACCCAG[C/G]TAGTTTTTGTATTTT | 7464 |
rs751789178 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191253 | TCCGGACCTCTCAGA[C/G]GGTCCCCAGGAGGGG | 7464 |
rs751850075 | snp | C/T | 3.31873e-05 | 0.0040734 | splice-acceptor-variant | CORO2A | GRCh38.p7 | 9:98128261 | TTGGTAGGATTCTGA[C/T]TGCAGGAGAAATCCA | 7464 |
rs751851475 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128064 | CATGGCTTCTGAGGT[C/T]ATGAGAGAAGAAAAA | 7464 |
rs751928169 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176431 | CCTGCTGGGGGAAGA[C/T]GTGCTCAACCAGTGG | 7464 |
rs751932580 | snp | A/G | 1.65414e-05 | 0.00287583 | missense | CORO2A | GRCh38.p7 | 9:98128178 | TCCTCACCTCGATTC[A/G]TCCCGCTGAGCCACT | 7464 |
rs751953797 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157601 | GCAGTTCTCCTTGCT[A/G]GCTGGTTTGCCAAAG | 7464 |
rs751954225 | snp | C/T | 3.36899e-05 | 0.00410412 | intron-variant | CORO2A | GRCh38.p7 | 9:98132997 | CCCCACTCTGCTCCT[C/T]GCTCCTCTGAGCCTG | 7464 |
rs752010476 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150867 | GCACTTGTCCCTCCC[C/T]AGCTCGAAACATTCT | 7464 |
rs752011509 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139484 | AATACAAAATTAGCC[A/G]GGCGTGGTGGCACAT | 7464 |
rs752054375 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150167 | CAAACTCCTGACCTC[A/G]TGATCTGCCTGCCTC | 7464 |
rs752115336 | snp | C/T | | | missense | CORO2A | GRCh38.p7 | 9:98126614 | TCAGCCAGGTTTTCT[C/T]CTCCTCCAGCCTGTG | 7464 |
rs752137857 | snp | A/C | 1.64841e-05 | 0.00287085 | intron-variant | CORO2A | GRCh38.p7 | 9:98157701 | GTATGAGGCTCACTG[A/C]CCTGATCATGGGACA | 7464 |
rs752178056 | snp | A/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186656 | ACTTCATGAGATATC[A/T]TTTACATATAATATA | 7464 |
rs752180652 | in-del | -/CAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171401 | CAGAGTCAGTTCAGC[-/CAA]CATCATTGGTGCCCA | 7464 |
rs752181596 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151015 | TGGCCAGACAGCTGC[C/T]CTCTGCATTGCTTCC | 7464 |
rs752225814 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171195 | TTTCAGACCTGTCTT[C/T]GGACAGAGAGGGACA | 7464 |
rs752285658 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149395 | AGCTCTGATTAGTGG[C/T]TCCTGGGTGTGTTAG | 7464 |
rs752288468 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186742 | TGGGGATTGGGTTAA[C/T]GTATATAAAATATTA | 7464 |
rs752326214 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129885 | GTAGCGGATGTTGCC[A/G]TCTCCCTGAGGAGGA | 7464 |
rs752414014 | snp | A/G | 3.29516e-05 | 0.00405891 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129813 | CCCCTTCTGTGGGTT[A/G]TAGGAGCGGTACTCA | 7464 |
rs752453110 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171797 | GCAAATGCAGGCCAG[C/T]AATGGGGCTGCCGCT | 7464 |
rs752457000 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181685 | AGGGCTTTGGCAAGG[C/G]TGTTTCTCCTATGCA | 7464 |
rs752473914 | snp | C/G | 3.35734e-05 | 0.00409702 | intron-variant | CORO2A | GRCh38.p7 | 9:98134973 | GGCAGGGGAGACAGG[C/G]CCCAAGGCAGCATTA | 7464 |
rs752488033 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137073 | TAACACTGAACATTG[C/T]TGGGGCAGGGATGAT | 7464 |
rs752615673 | in-del | -/AG | 2.78439e-05 | 0.00373111 | intron-variant | CORO2A | GRCh38.p7 | 9:98126918 | CATGCAGAGACACTC[-/AG]AGCCATGCAGACCCA | 7464 |
rs752668741 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159529 | TGCATCTCCAGCCCT[C/T]TGGCTCTTTGCCCGT | 7464 |
rs752748473 | snp | C/T | 3.32602e-05 | 0.00407786 | intron-variant | CORO2A | GRCh38.p7 | 9:98128160 | TGGGCCTCTTCTCTG[C/T]CTTCCTCACCTCGAT | 7464 |
rs752760967 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179090 | TTGGTTGGGTTCACT[C/G]TGAAGCCTCAGTTTC | 7464 |
rs752803590 | snp | A/C | 4.16832e-05 | 0.00456507 | intron-variant | CORO2A | GRCh38.p7 | 9:98131106 | GGTCACTCCTGGGGG[A/C]CCTCAGTGGTGCTCC | 7464 |
rs752865482 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159525 | CTCTTGCATCTCCAG[A/C]CCTCTGGCTCTTTGC | 7464 |
rs752903594 | snp | A/C | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194343 | AACATTGTGGGAATT[A/C]TTTATAATCATGGTT | 7464 |
rs752910123 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CORO2A | GRCh38.p7 | 9:98137643 | CATCCAAAACGTTGC[C/T]TCTGTGCCCGCAGAC | 7464 |
rs752913288 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158575 | TTACAGGAGTGAAGA[A/G]TCCTCTGGGTGAGGC | 7464 |
rs752921550 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147279 | TGTGATCCTGGCATT[A/C]TGGTTATGTCAGAAA | 7464 |
rs752949174 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166827 | TTCAAACCATGGAAT[A/G]ATATTCAACCTTCAA | 7464 |
rs753001624 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144620 | GAGGCACACAAGAGA[-/C]CCTGGGGGATGAACC | 7464 |
rs753085117 | snp | A/G | 1.67111e-05 | 0.00289055 | intron-variant | CORO2A | GRCh38.p7 | 9:98128290 | CAGACAGTGAGGAGG[A/G]TGGTAGGGTAGGCTG | 7464 |
rs753091945 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167621 | GTGTGGATCCTGTGT[A/G]GATCCGGATTCACAC | 7464 |
rs753158246 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129385 | AAGTGGGTTTCTTGT[A/T]GATTACAGAAATATA | 7464 |
rs753202240 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176463 | CTTCCTCGCATCTAC[C/T]GAACAGAAATCTACA | 7464 |
rs753214936 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166587 | TGCAAAAGGGTTTAG[C/T]TGCTATGAAAGATAG | 7464 |
rs753250461 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127469 | ACAGGCAGAGTGGGC[A/C]GAGGGACCTGGGTGG | 7464 |
rs753334909 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153320 | TGGCCAGGCTGATGT[C/T]GAACTCCTGACTTCA | 7464 |
rs753337134 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139788 | GCAACAGAATGGGAC[C/T]CTGTCTCAAACAAAA | 7464 |
rs753384577 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162220 | AGCCTGCAGCTCCAG[A/G]TCCTCACAGACAATA | 7464 |
rs753412045 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178348 | TCAACCTCTTCCATT[C/T]CCTTGTCTTCATGTA | 7464 |
rs753436636 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133095 | GCGGTCTTTGCAGGT[A/G]GTGGCCAACAGGCTG | 7464 |
rs753466296 | in-del | -/TG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167953 | TCCTTTAATTTTGTA[-/TG]TGTCTTTAAATTTCC | 7464 |
rs753476322 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152182 | CTCAATGTTTAGTAG[C/T]TAGAGGACTATTCAG | 7464 |
rs753494778 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152409 | AGCCTCCTGCCTCAG[C/T]CTTCTGAGTAGCTGG | 7464 |
rs753553159 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | CORO2A | GRCh38.p7 | 9:98126617 | GCCAGGTTTTCTTCT[C/T]CTCCAGCCTGTGTTC | 7464 |
rs753553900 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171908 | TGACATGGTCAGAGC[C/T]GAAATAGACTTAACC | 7464 |
rs753570324 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98187986 | TAAAAAGAGTAGCTC[C/T]GTCATACACTCGCAG | 7464 |
rs753595574 | in-del | -/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156051 | CTCTTTGTTTGAATT[-/TTT]TTTTTTTTTTTTTTT | 7464 |
rs753600054 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192316 | ACCTCGAGGCGGCCC[C/T]TCCCAACAACCCCGC | 7464 |
rs753606061 | snp | A/C | 1.64738e-05 | 0.00286995 | missense | CORO2A | GRCh38.p7 | 9:98137599 | AGAACAGGAGGCGAT[A/C]TCAAAATCATCAAAA | 7464 |
rs753607370 | snp | C/T | 1.67733e-05 | 0.00289592 | intron-variant | CORO2A | GRCh38.p7 | 9:98126546 | CCCCGTCCTCCTTCA[C/T]ACCTCATTCTCTGTC | 7464 |
rs753628241 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133849 | GCATCAACCTCCTGG[G/T]CTCAAGTGATCCTCC | 7464 |
rs753663828 | snp | G/T | 1.67245e-05 | 0.00289171 | intron-variant | CORO2A | GRCh38.p7 | 9:98129932 | GGTGAGATTCAGAGC[G/T]GGAGCTCATCAGCTC | 7464 |
rs753734098 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140940 | GAACGGTAGATTACA[A/G]TATTATCACAACATT | 7464 |
rs753772913 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181901 | GTCACTTCCAAGCTG[C/T]GTGACCTCAGACAAG | 7464 |
rs753793631 | snp | C/G | 1.67534e-05 | 0.0028942 | intron-variant | CORO2A | GRCh38.p7 | 9:98128297 | TGAGGAGGGTGGTAG[C/G]GTAGGCTGCTCAGAT | 7464 |
rs753830165 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164440 | TGATCCACCCATTGC[C/G]AGTGGGATATCTGGC | 7464 |
rs753831797 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145870 | GGCATGTGCCACCAC[A/G]CCCAGCTGATTTTTT | 7464 |
rs753863016 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136388 | CTCTTTGAATTTTCT[A/G]CCTTCCTTTCCTGAT | 7464 |
rs753880915 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171293 | CTGTAACTCTGGTCC[C/T]GGGGTGGGCATCCAA | 7464 |
rs753892216 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182560 | TGTTCTTCCCAAGGG[A/C]CAGGACTCAGGAGCC | 7464 |
rs753892909 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175145 | TGACTTCAAAAGCAG[G/T]GGGTGGGGTGCGGGA | 7464 |
rs753893840 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159994 | ACGAGATTACACTGT[A/G]TGACCTCAGGCAAGT | 7464 |
rs753944150 | snp | C/T | 1.96794e-05 | 0.00313677 | intron-variant | CORO2A | GRCh38.p7 | 9:98126895 | GGGGCACCAATGACA[C/T]AGGCAGGCATGCAGA | 7464 |
rs753970862 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98124986 | CTATCCCTCTTTGAC[C/T]CAGAAAGGTGGAGGC | 7464 |
rs753979598 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181593 | GTTCTACTTCCCCAG[C/T]CTCACCTTGCCCAGG | 7464 |
rs754021079 | in-del | -/TATGAGGCTCACTGCCCTGATCATGGGA | 1.74087e-05 | 0.00295026 | intron-variant | CORO2A | GRCh38.p7 | 9:98157687 | AAATGGGACAAAGGG[-/TATGAGGCTCACTGCCCTGATCATGGGA]CACACAGAGCTCTCA | 7464 |
rs754021305 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149918 | TGTGTAGGACAAGTG[A/C]GTTTCTTTTTCTCTT | 7464 |
rs754054398 | snp | A/G | 1.65479e-05 | 0.0028764 | intron-variant | CORO2A | GRCh38.p7 | 9:98132165 | AGGGGTGATGGTGAG[A/G]GGTGGGGTGCAGCCC | 7464 |
rs754099206 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148893 | AAAAAAGCCAAGCTG[A/T]AAAGGTTACATATTG | 7464 |
rs754106687 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135404 | CTAGGGAGCCGGCGA[C/G]GTCTCTGCAGCAGGG | 7464 |
rs754166177 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130572 | GGGGAACATTTCTGG[C/T]TGTCATAATGACTTG | 7464 |
rs754196820 | snp | C/T | 2.02723e-05 | 0.00318366 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124733 | ACCTCCCCATGGAGC[C/T]GAGTGGTGTCCCTGA | 7464 |
rs754211156 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181357 | TTTTTTTTTTTTTTT[-/C]AAGAGATGAGGTCTC | 7464 |
rs754221032 | snp | G/T | 1.64909e-05 | 0.00287144 | intron-variant | CORO2A | GRCh38.p7 | 9:98137735 | GAGGTGGATTCCACA[G/T]TAGCATCTGGACAGT | 7464 |
rs754231931 | snp | C/G | 3.29723e-05 | 0.00406018 | missense | CORO2A | GRCh38.p7 | 9:98128614 | GCCCTTACCCGCCGG[C/G]GCACAATCATGGAGA | 7464 |
rs754234351 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159673 | CCTTGATATCCCAAG[C/T]AGCAGAGATCTCGCT | 7464 |
rs754268225 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147443 | GATAATTCTAGAATC[C/T]GGGCTGAGGAAAGTT | 7464 |
rs754330658 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167774 | TTATCTTTTAGAGAC[A/G]GATGCCTAATATTCA | 7464 |
rs754376905 | in-del | -/AAAC | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173143 | TTCTGTCTCTACAAA[-/AAAC]AAACAAACAAACAAA | 7464 |
rs754386909 | in-del | -/C | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120545 | ACTTTCACACACACA[-/C]CACCACCCCAAATTC | 7464 |
rs754497067 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125073 | ACACCTTGTTTACTT[-/C]CACCCAATAAATGAA | 7464 |
rs754588887 | snp | C/T | | | missense | CORO2A | GRCh38.p7 | 9:98130959 | GCCAAGCCGACCTTC[C/T]CCACCACGTAGAGCA | 7464 |
rs754592164 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185549 | CATTGCTGGAGGCTC[A/G]TATCTGATTTCTCAG | 7464 |
rs754641035 | snp | G/T | 1.99663e-05 | 0.00315955 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124758 | CCCTGAGGGTGAGGA[G/T]GGCAGAGGTCTCTGC | 7464 |
rs754676609 | snp | A/C | 1.74961e-05 | 0.00295766 | intron-variant | CORO2A | GRCh38.p7 | 9:98128769 | CTAGGCTGGGGCCAC[A/C]GTGTTAGGGCCAAAG | 7464 |
rs754737809 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189784 | CCAGACTCCGGTAAT[A/G]TAAGCTTCAGTGCCA | 7464 |
rs754777234 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168952 | CATCTCTCCGGGCTG[G/T]GTTCTCCTAGGTGGA | 7464 |
rs754837627 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142730 | GAAGGGCCTAGCCCT[A/G]GACAGCTTCTCTTCC | 7464 |
rs754847218 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189296 | TGTGATTGCAAAGCA[C/T]GTCCAATCTGTTCTG | 7464 |
rs754855470 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164253 | CTCTATGTGAAGGTG[A/C]TCTACAAAGGCTGAG | 7464 |
rs754862569 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180617 | CATCCCTTCTTTTGA[C/T]TGCACAGTGAACTCT | 7464 |
rs754870538 | snp | C/T | 3.70865e-05 | 0.00430603 | missense | CORO2A | GRCh38.p7 | 9:98134813 | AGACTCACCTTGTAG[C/T]CATAGCCAGCACTGA | 7464 |
rs754948928 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153943 | AAACACTTTTTCTCC[A/G]TCTATGGACATGATC | 7464 |
rs755043183 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182656 | CTTTGCCTCTTGCTG[C/G]CTGCGTGACCTTGCA | 7464 |
rs755068620 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147256 | GGTGACACAAGAGTT[A/C]TTATTAATGTGATCC | 7464 |
rs755132465 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182065 | TTCTCTACTCTGCAC[A/G]CCCTTCACTCCTCTC | 7464 |
rs755176659 | snp | A/C/T | 3.30617e-05 | 0.00406568 | missense | CORO2A | GRCh38.p7 | 9:98157486 | GGATGACGAGGAAGG[A/C/T]CCCTCCACCAGCACA | 7464 |
rs755177762 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CORO2A | GRCh38.p7 | 9:98137637 | ACTTGACATCCAAAA[C/T]GTTGCCTCTGTGCCC | 7464 |
rs755199037 | snp | A/G | 3.31989e-05 | 0.00407411 | intron-variant | CORO2A | GRCh38.p7 | 9:98128263 | GGTAGGATTCTGACT[A/G]CAGGAGAAATCCAGA | 7464 |
rs755227101 | snp | C/T | 1.65422e-05 | 0.0028759 | intron-variant | CORO2A | GRCh38.p7 | 9:98137521 | ATTCCACCCCAACCA[C/T]CCCAATCCCACTCTT | 7464 |
rs755230158 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146128 | GCCTGTCTACTCCCA[A/G]CAGGGTTCCAGGGCT | 7464 |
rs755266158 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158315 | GAGAGATTGAAAAAA[C/G]TATCTGCCTCATAGC | 7464 |
rs755316190 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166581 | TAGGAATGCAAAAGG[A/G]TTTAGTTGCTATGAA | 7464 |
rs755361265 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191258 | ACCTCTCAGACGGTC[C/T]CCAGGAGGGGCAGGA | 7464 |
rs755397566 | snp | C/T | 4.96184e-05 | 0.00498063 | missense | CORO2A | GRCh38.p7 | 9:98128179 | CCTCACCTCGATTCA[C/T]CCCGCTGAGCCACTC | 7464 |
rs755448479 | snp | A/G | 1.67668e-05 | 0.00289537 | intron-variant | CORO2A | GRCh38.p7 | 9:98133012 | TGCTCCTCTGAGCCT[A/G]AGCCAGCCCCTGGCC | 7464 |
rs755476843 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175360 | CCACCAACCTCCCTC[C/T]TCCTGGTGAAGGAAG | 7464 |
rs755503339 | snp | A/G | 1.65485e-05 | 0.00287645 | intron-variant | CORO2A | GRCh38.p7 | 9:98132309 | CTGGCCTCCTGGAGG[A/G]ACACGTGCGGTCGGT | 7464 |
rs755508095 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186685 | TATCCATTTTAAAAC[A/G]GGAGAAATAATAACA | 7464 |
rs755533060 | snp | G/T | 0.00393057 | 0.0441569 | missense | CORO2A | GRCh38.p7 | 9:98157607 | CTCCTTGCTGGCTGG[G/T]TTGCCAAAGACATGA | 7464 |
rs755541246 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182151 | GTGAGCCCTCAAAGG[C/T]GGGCCTGTGTCTGTT | 7464 |
rs755557387 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138110 | TTCCACTCCTAGGTC[A/T]ATCTCCATGGAAAAT | 7464 |
rs755642276 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152021 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGCTCTC | 7464 |
rs755651296 | snp | C/G | 1.671e-05 | 0.00289045 | intron-variant | CORO2A | GRCh38.p7 | 9:98133019 | CTGAGCCTGAGCCAG[C/G]CCCTGGCCCAGAACT | 7464 |
rs755715770 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171419 | CATCATTGGTGCCCA[C/G]TCTGAGCCTGATGCC | 7464 |
rs755756305 | snp | C/G | 1.77407e-05 | 0.00297826 | intron-variant | CORO2A | GRCh38.p7 | 9:98157705 | GAGGCTCACTGCCCT[C/G]ATCATGGGACACACA | 7464 |
rs755774559 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132929 | GCTGCCTGTGAAGGC[A/G]CAGCCCAGACGCTGA | 7464 |
rs755775255 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129888 | GCGGATGTTGCCATC[C/T]CCCTGAGGAGGAGGA | 7464 |
rs755801849 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151020 | AGACAGCTGCTCTCT[A/G]CATTGCTTCCTGAAC | 7464 |
rs755967926 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | CORO2A | GRCh38.p7 | 9:98129814 | CCCTTCTGTGGGTTA[C/T]AGGAGCGGTACTCAG | 7464 |
rs755983309 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180889 | CATGCTCAGCAACAC[C/T]TTTGCTGAAAGACCA | 7464 |
rs755985828 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137273 | CTTTTATAGCTCCCC[A/G]AAGGATGGGTTTTCC | 7464 |
rs756008262 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131935 | CCAGACTCAGCTACC[A/T]CCCCTCCTCTAGCCA | 7464 |
rs756165418 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174352 | AGCAGTGCTTGGCAA[A/G]TGCTCAGCCAGGTGT | 7464 |
rs756277395 | snp | A/C | 6.58892e-05 | 0.00573936 | stop-gained | CORO2A | GRCh38.p7 | 9:98126656 | ACCTTGGCATCTTCT[A/C]CTCCAACAGGGAGGA | 7464 |
rs756310990 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183611 | CAGATGGAAAATATT[C/T]GAAAAAATTAAGGAA | 7464 |
rs756372780 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134309 | CCTGCATGCTTGATT[A/G]TCAGTGGAGCAGGGT | 7464 |
rs756372826 | in-del | -/CC | 0.00010008 | 0.00707319 | intron-variant | CORO2A | GRCh38.p7 | 9:98128569 | TCTCCAGGACAGGTT[-/CC]CCCCACCTGCCTCCC | 7464 |
rs756373300 | snp | A/G | 3.48426e-05 | 0.00417374 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98130988 | CATGCTGGTGTCCGC[A/G]TCATAGAAGGGAAAC | 7464 |
rs756377325 | snp | G/T | 1.64882e-05 | 0.00287121 | intron-variant | CORO2A | GRCh38.p7 | 9:98137728 | TGGGGAGGAGGTGGA[G/T]TCCACATTAGCATCT | 7464 |
rs756406880 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129481 | AGGTCAGCCCTTTCC[A/G]TCTCTGCTCTTGTGG | 7464 |
rs756416497 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146996 | TATTGGCCAGGTGTG[A/G]TGGCTCATGCCTGTT | 7464 |
rs756439713 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144643 | GATGAACCAGAGAAG[G/T]CTCCCTGGAGGAGGA | 7464 |
rs756457570 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | CORO2A | GRCh38.p7 | 9:98157570 | GAACGCTGCGGGTGA[C/T]AGGCACGGAGTCGTA | 7464 |
rs756483882 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173513 | CCAACTCGGTGGCCA[-/C]TGCGGCTCTGCTCCT | 7464 |
rs756492505 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | CORO2A | GRCh38.p7 | 9:98128611 | ACTGCCCTTACCCGC[C/T]GGGGCACAATCATGG | 7464 |
rs756531515 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165238 | TGCTGGGATGACAGG[C/T]GTGAGCCACCGTGCC | 7464 |
rs756540105 | snp | A/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194372 | TTTGGTTTTTACTTG[A/T]ATTACAGCTGGACGG | 7464 |
rs756540186 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182753 | CAATGCGATGGTGAA[A/G]ATTCCATGAGTGAAT | 7464 |
rs756574124 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139583 | GGTGAGCTGAGATTG[C/T]GCCACTGCGTTCCAG | 7464 |
rs756664337 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155753 | TTTTTTAAGGAGTTT[-/G]CCCATATTGTTAATG | 7464 |
rs756684046 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178408 | TGCTAACAAGTCACA[A/G]TTTTTCAGTACGAAT | 7464 |
rs756705426 | snp | A/G | 1.6525e-05 | 0.00287441 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128240 | TGTTGGAGGGTATAT[A/G]TCCTCTTGGTAGGAT | 7464 |
rs756784251 | snp | C/T | 1.68272e-05 | 0.00290057 | intron-variant | CORO2A | GRCh38.p7 | 9:98128307 | GGTAGGGTAGGCTGC[C/T]CAGATGGGAAAGGCC | 7464 |
rs756791200 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141229 | CCTCTTCTACAGCAG[A/G]ACAGGGGAGAGAGGT | 7464 |
rs756803577 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179670 | AGGGAGGTGAGCAGT[C/T]GGCCGGGCGCAGACA | 7464 |
rs756862756 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154538 | TCTCCCACGAGATGC[C/T]TTCCAGTCGTAACCC | 7464 |
rs756877448 | in-del | -/CAAA | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194290 | GGACTCTGTCTCAAA[-/CAAA]CAAACAAACAAACAA | 7464 |
rs756883187 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188075 | CTTCCTCTTCTCCCG[C/T]CATCACTCTGTCCCA | 7464 |
rs756890221 | snp | C/T | 1.64849e-05 | 0.00287092 | missense | CORO2A | GRCh38.p7 | 9:98133190 | TTGTGATGACAGACT[C/T]CTTTGTATCCAGGTT | 7464 |
rs756903551 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126621 | GGTTTTCTTCTCCTC[C/T]AGCCTGTGTTCTGCT | 7464 |
rs756921021 | snp | G/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122654 | TACTACTTCTTTACC[G/T]CGTATAGTCATTTCA | 7464 |
rs756930473 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152436 | CTGGGACTACAGGCA[C/T]GCTCCACTATGCCTG | 7464 |
rs756943533 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | CORO2A | GRCh38.p7 | 9:98133111 | GTGGCCAACAGGCTG[C/G]CGTTGGTGTTGAAGG | 7464 |
rs756956668 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139830 | GTGAATTTTCTGGTA[C/T]GTGAATTCTACCTCA | 7464 |
rs757047116 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133856 | CCTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA | 7464 |
rs757078912 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145881 | CCACGCCCAGCTGAT[C/T]TTTTATTTTTGGTAG | 7464 |
rs757088069 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120731 | AATGCCCTTTGCCCT[A/G]AGTATTCCAACTTAC | 7464 |
rs757090302 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162356 | AAAATGAGGCCCAGG[A/G]AGCTAGCTAGAACCC | 7464 |
rs757097881 | snp | C/G | 3.61566e-05 | 0.0042517 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98130964 | GCCGACCTTCCCCAC[C/G]ACGTAGAGCATGCTG | 7464 |
rs757107247 | in-del | -/GAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141197 | TGAAAATTTTCTCTC[-/GAAA]TTTCAAGTGGTCTCT | 7464 |
rs757153631 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132142 | TGAATGACACTGGCT[C/T]TCAGCTGAGGGGTGA | 7464 |
rs757157810 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192526 | CATCGCGCAGACCGG[A/G]AAGGCACGGCCGGCG | 7464 |
rs757164347 | snp | C/T | 1.7174e-05 | 0.00293031 | intron-variant | CORO2A | GRCh38.p7 | 9:98135004 | GCCAGGGCACCTTGG[C/T]ACCGTCACCAGCCTA | 7464 |
rs757176644 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190815 | CACTTAAGCCTGTGC[A/G]TCGGAGCTGGGCTCA | 7464 |
rs757199450 | snp | G/T | | | missense | CORO2A | GRCh38.p7 | 9:98133121 | GGCTGCCGTTGGTGT[G/T]GAAGGACATGGAGAG | 7464 |
rs757228947 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171314 | GGGCATCCAACCAGG[A/G]GTCCTGCATTCTGTT | 7464 |
rs757359603 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135493 | GAAGGTCAGGAGGCT[A/G]GGCTGGATGGGGTCA | 7464 |
rs757416518 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133240 | GCAGAGAGCCAGCTC[G/T]GAGCACAGGGGCCAC | 7464 |
rs757441514 | snp | C/T | 1.65477e-05 | 0.00287638 | intron-variant | CORO2A | GRCh38.p7 | 9:98132168 | GGTGATGGTGAGGGG[C/T]GGGGTGCAGCCCTCA | 7464 |
rs757450247 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160115 | GCTCAGAAATTCCAA[C/G]TCTCCTTTCGGGAGC | 7464 |
rs757466536 | snp | A/C | 1.65258e-05 | 0.00287448 | missense | CORO2A | GRCh38.p7 | 9:98132261 | TTCAGGTTCCCCAGA[A/C]ACAGCACTTTGCTGG | 7464 |
rs757469700 | snp | A/T | 6.57109e-05 | 0.00573159 | intron-variant | CORO2A | GRCh38.p7 | 9:98126905 | TGACACAGGCAGGCA[A/T]GCAGAGACACTCAGA | 7464 |
rs757479798 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190041 | AGGCATGTGCCACCA[C/T]ACCCAGCTAATTTTT | 7464 |
rs757488028 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149995 | GGAGTGCAGTGGCGC[A/G]ATCTTGACTCACTGC | 7464 |
rs757520567 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | CORO2A | GRCh38.p7 | 9:98157512 | GCACACTCAGTCACA[A/G]CTGCAATGAAGTGGG | 7464 |
rs757521278 | snp | C/T | 1.65072e-05 | 0.00287286 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126783 | CAGTGGGTGGGGTCT[C/T]AGCAGCTCAGAGCCA | 7464 |
rs757536907 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123741 | GTTCACTGCAACCTC[C/T]GCCTCCCAGGCTCAA | 7464 |
rs757678234 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173595 | CCAGCACTCCGGAAC[C/T]GGGCGTCCCAATCCT | 7464 |
rs757719728 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148554 | AGACCAACCTGAGCA[A/C]CATAGCAAAACCTCA | 7464 |
rs757782025 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175157 | CAGGGGGTGGGGTGC[-/G]GGATGGCCCTCCCTG | 7464 |
rs757795626 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168810 | AGCAGCCTCCCAGGG[C/G]CCAAGTGGCTCGTGA | 7464 |
rs757796002 | snp | C/T | 1.64827e-05 | 0.00287073 | missense | CORO2A | GRCh38.p7 | 9:98128618 | TTACCCGCCGGGGCA[C/T]AATCATGGAGATGGG | 7464 |
rs757796310 | snp | A/C/G | 2.19942e-05 | 0.00331612 | intron-variant | CORO2A | GRCh38.p7 | 9:98134796 | CCAGAGAAAGAATAC[A/C/G]CAGACTCACCTTGTA | 7464 |
rs757808539 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194464 | ATGGTTTTGTTCTGT[C/T]GCCCAGGCTGGAGTG | 7464 |
rs757809121 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152125 | CCGGCCTCTTTTGCT[-/G]GTTTTTTTTTTTTGT | 7464 |
rs757827628 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158732 | AGTTGGTCATGTAGG[C/T]AGGATGAGGGAGAGC | 7464 |
rs757829117 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144809 | GCTGGAGGACAGGGC[A/C]AGAGAGGAGGCTGAG | 7464 |
rs757926881 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169981 | CATTTGGGGAGGTAG[A/C]CAAAGGCAGGGAAAA | 7464 |
rs757933823 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130891 | TGTTCCCAATGGCCC[C/T]AGGCTGCTGTCTGCC | 7464 |
rs757943415 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187459 | GCGAAACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 7464 |
rs758011313 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179675 | GGTGAGCAGTCGGCC[A/G]GGCGCAGACACTCAG | 7464 |
rs758041069 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157306 | TATTTTTCCCAGTGA[A/G]GAAACCAAGGCTCAA | 7464 |
rs758042497 | snp | A/G | 1.68818e-05 | 0.00290527 | intron-variant | CORO2A | GRCh38.p7 | 9:98128742 | CAGACAGGGAGGGCC[A/G]AGAGGTTCTGGCTAG | 7464 |
rs758052925 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127819 | CGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 7464 |
rs758090499 | snp | A/G | 1.64974e-05 | 0.00287201 | missense | CORO2A | GRCh38.p7 | 9:98133201 | GACTCCTTTGTATCC[A/G]GGTTCCAGATCATCA | 7464 |
rs758105360 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129931 | GGGTGAGATTCAGAG[C/T]TGGAGCTCATCAGCT | 7464 |
rs758118301 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151814 | ACCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 7464 |
rs758202512 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134127 | GTCAAAAGGAAAGAA[C/G]TGAAAGGCCATAGCT | 7464 |
rs758266065 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | CORO2A | GRCh38.p7 | 9:98126761 | TGAAGATAGGTCTCT[C/T]TGCAGGCAGTGGGTG | 7464 |
rs758284277 | snp | C/G | 3.55549e-05 | 0.00421618 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98130970 | CTTCCCCACCACGTA[C/G]AGCATGCTGGTGTCC | 7464 |
rs758312562 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152675 | ATAATGTGACAAACT[A/G]ACATCATGTGTCCCA | 7464 |
rs758400527 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162462 | TCCGTCCCCCAATCC[C/T]CTCCCCACCCTAACT | 7464 |
rs758417563 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141374 | TTTTTTTTTTGGACA[C/T]GGAGTCTCGTCTTGT | 7464 |
rs758453927 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163124 | GATTAGGCTCCGGGG[C/T]CTGTGAATTCCCAAC | 7464 |
rs758476447 | in-del | -/G | 1.66877e-05 | 0.00288852 | intron-variant | CORO2A | GRCh38.p7 | 9:98128285 | AAATCCAGACAGTGA[-/G]GAGGGTGGTAGGGTA | 7464 |
rs758493030 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125386 | AGTGCTAGTGTCCCC[A/G]CCGTACCACCGTGGA | 7464 |
rs758528283 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144789 | GCAGCCAGCGGGCAC[C/G]GTAGGCTGGAGGACA | 7464 |
rs758535551 | snp | G/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192869 | TGATTGGGGCGGGCT[G/T]CCGGCCACCAGGCGG | 7464 |
rs758558528 | snp | A/C/T | 8.96389e-05 | 0.00669424 | intron-variant | CORO2A | GRCh38.p7 | 9:98126942 | CAGACCCATGCAACA[A/C/T]GTGTGGGAAATACAG | 7464 |
rs758606282 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181990 | ATACCTTCCTTTCCT[C/T]GACCGGCACCATCTG | 7464 |
rs758607762 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165319 | TCAAGTTGTCTGCGA[A/G]AGAGGAGGCTCTAGA | 7464 |
rs758624763 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138073 | CCTCAAAAGGTTAAC[A/C]GGTTCCCACATGACC | 7464 |
rs758631936 | snp | G/T | 8.43604e-05 | 0.00649408 | intron-variant | CORO2A | GRCh38.p7 | 9:98132991 | CTCTGTCCCCACTCT[G/T]CTCCTTGCTCCTCTG | 7464 |
rs758660815 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156204 | GCCCTCATGCCCAGT[C/T]AATTTTTGTATTTTT | 7464 |
rs758879298 | snp | A/C | 1.64857e-05 | 0.00287099 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157532 | AATGAAGTGGGGGTT[A/C]ACGGCACAGAAGTGG | 7464 |
rs758934534 | snp | A/C | 0.000162714 | 0.00901835 | intron-variant | CORO2A | GRCh38.p7 | 9:98157387 | AGGACTTTCTAGAAA[A/C]CCAGGCTCTTTCCAC | 7464 |
rs758943511 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160583 | AACAAGGACAAATGA[A/C]CTCCCTAGGGTCTTG | 7464 |
rs758973047 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148671 | ATTGCTTGAGCCCAG[G/T]AAGTGGAGGCTTCAG | 7464 |
rs758983217 | snp | A/C/G | 4.00555e-05 | 0.00447509 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124751 | GTGGTGTCCCTGAGG[A/C/G]TGAGGAGGGCAGAGG | 7464 |
rs758991094 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139814 | CAAAAAACAAAACAC[A/G]GTGAATTTTCTGGTA | 7464 |
rs759000152 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171116 | GATTTTCCAAGACAC[A/C]TCCAGGAGGCTGAAA | 7464 |
rs759039457 | in-del | -/G | 1.68687e-05 | 0.00290414 | intron-variant | CORO2A | GRCh38.p7 | 9:98126853 | GAGCCATGTGAGGAC[-/G]GGGTGCCCACGGGAA | 7464 |
rs759053267 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171671 | GCAAGCCCAGCAGAG[A/G]AGGGAAGGGGAGGCA | 7464 |
rs759087584 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146747 | CTCCCATTCGGGTCC[C/T]GGACACACTGCACAG | 7464 |
rs759115810 | in-del | -/C | 3.36137e-05 | 0.00409948 | intron-variant | CORO2A | GRCh38.p7 | 9:98133260 | ACAGGGGCCACCTTG[-/C]CCCTGGGCCTCATAG | 7464 |
rs759196937 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156766 | GATTCATATTTCTCT[A/G]TGTTTAATCTGTGGG | 7464 |
rs759257329 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159448 | CTGGGTCTCATTCCA[C/T]ATTCCAAGATTCTTT | 7464 |
rs759281662 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165872 | GACCTACTGAATCAG[A/G]TATTCTGGGGGTGGG | 7464 |
rs759308124 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190881 | GGGATAATAACACTC[A/G]TTTGTGGTCCAGCTC | 7464 |
rs759317654 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145589 | GGCTAGGACAGGGCA[C/T]AGAGGGCTTTGATGA | 7464 |
rs759335832 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122688 | GACCTCCTGGTTAGG[C/T]GGCCAGAGGCTCTGC | 7464 |
rs759397205 | in-del | -/AG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158295 | TAAAAAAAAAATAAA[-/AG]AGAGAGAGATTGAAA | 7464 |
rs759401045 | snp | C/G | 1.65113e-05 | 0.00287322 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128204 | CCACTCCTGGGCCGT[C/G]AGGGAGGGCTGGGCC | 7464 |
rs759452151 | snp | G/T | 1.67466e-05 | 0.00289362 | intron-variant | CORO2A | GRCh38.p7 | 9:98128139 | CATGTTCCTGTCACA[G/T]TTGCCTGGGCCTCTT | 7464 |
rs759471016 | snp | A/G | 1.73776e-05 | 0.00294762 | intron-variant | CORO2A | GRCh38.p7 | 9:98126869 | GGGTGCCCACGGGAA[A/G]ATGGGCATATGGGGC | 7464 |
rs759503557 | snp | A/T | 1.65704e-05 | 0.00287836 | intron-variant | CORO2A | GRCh38.p7 | 9:98132326 | CACGTGCGGTCGGTA[A/T]TGGAGAGACAGTAGA | 7464 |
rs759514410 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175076 | GTTGATTTCCACAGA[A/G]CTCCTATTCTTTTAG | 7464 |
rs759541632 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98124908 | ACATCTGCAGCAACT[A/G]GGGAAGAAAGATCGG | 7464 |
rs759545281 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183532 | AATATCATTATAACT[C/T]GTATTGCATACATAG | 7464 |
rs759553687 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159367 | ATCACCCTCTGATGC[C/T]GCCCATTCATTGCTG | 7464 |
rs759557067 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165185 | GCTGGTCTTGAACAC[C/G]TGGCCTCAGGCGATC | 7464 |
rs759614958 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189663 | AGAGGGGAACGGATC[-/G]GCCCAAGGTCACACA | 7464 |
rs759625733 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146409 | TCACAACAGGCAAGA[G/T]GGAGGGACCCTGCCT | 7464 |
rs759654091 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128679 | GTAGAAGCGGAAGAT[C/T]TCGCAGGAGGACACG | 7464 |
rs759657007 | in-del | -/CTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181258 | CACCCACGTGGCCTC[-/CTT]CTTCTTGTACCCAAT | 7464 |
rs759707070 | snp | C/T | 1.65059e-05 | 0.00287275 | intron-variant | CORO2A | GRCh38.p7 | 9:98128601 | TGCGGTCCCGACTGC[C/T]CTTACCCGCCGGGGC | 7464 |
rs759709294 | snp | A/G | 3.31939e-05 | 0.0040738 | intron-variant | CORO2A | GRCh38.p7 | 9:98133232 | CCTGCATGGCAGAGA[A/G]CCAGCTCTGAGCACA | 7464 |
rs759742735 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140928 | AAATCTAAACAAGAA[C/T]GGTAGATTACAGTAT | 7464 |
rs759762430 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | CORO2A | GRCh38.p7 | 9:98133154 | TCACATCTTGGTGAC[A/G]GCTAATCGTACTCAT | 7464 |
rs759782656 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189893 | ACTCCTTTATTTTTT[-/A]TTTTTTTTTGAGATG | 7464 |
rs759803783 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167499 | AATGAAATATACATA[C/T]ATTTTTTAAAAGATC | 7464 |
rs759845664 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139487 | ACAAAATTAGCCGGG[C/T]GTGGTGGCACATGCC | 7464 |
rs759915062 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133610 | CAATCCATTCCTATA[A/G]ACTAGGACGTGACTA | 7464 |
rs759931522 | snp | A/G | 6.89394e-05 | 0.00587068 | intron-variant | CORO2A | GRCh38.p7 | 9:98157676 | CTGCAGGAGACAAAT[A/G]GGACAAAGGGTATGA | 7464 |
rs759952460 | snp | C/T | 6.59011e-05 | 0.00573988 | missense | CORO2A | GRCh38.p7 | 9:98133081 | ATAACCCGAATCTTG[C/T]GGTCTTTGCAGGTGG | 7464 |
rs759962538 | snp | A/G | 2.03535e-05 | 0.00319004 | intron-variant | CORO2A | GRCh38.p7 | 9:98130942 | GGTCACCTCCCTCCC[A/G]TGCCAAGCCGACCTT | 7464 |
rs760091542 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174576 | CCCCAAGTGTGGAGG[A/G]AGGGGCCTGGTGAGA | 7464 |
rs760096970 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126720 | TGTCTGATTCAAGAG[C/T]CGGGGTGAGGCTGGG | 7464 |
rs760185598 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173082 | GGCCGAGGTGGGAGG[A/G]TCGCTTAGGGCCAGG | 7464 |
rs760191410 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146979 | TTACTTAATAAGAAA[C/T]ATATTGGCCAGGTGT | 7464 |
rs760222664 | snp | C/T | 1.91053e-05 | 0.00309068 | missense | CORO2A | GRCh38.p7 | 9:98131032 | AGCCGTCCAGGTCCT[C/T]CTCCATCAGAGGCAC | 7464 |
rs760257168 | in-del | -/GC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145918 | GGTTTTGGTATGTTG[-/GC]CAGGCTAGTCTCGAA | 7464 |
rs760275641 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193958 | CAGGTAGACTGAACG[C/T]ATGCTTCTGGTGTTA | 7464 |
rs760279831 | snp | A/G | 1.90297e-05 | 0.00308455 | intron-variant | CORO2A | GRCh38.p7 | 9:98130952 | CTCCCGTGCCAAGCC[A/G]ACCTTCCCCACCACG | 7464 |
rs760280049 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126615 | CAGCCAGGTTTTCTT[C/T]TCCTCCAGCCTGTGT | 7464 |
rs760294472 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187872 | CTTCCATGGCTCCCC[A/G]CTGACCCTGGCTGAA | 7464 |
rs760302166 | in-del | -/TCT | 1.6473e-05 | 0.00286988 | cds-indel | CORO2A | GRCh38.p7 | 9:98126685 | GAAGACCTCCAGCCA[-/TCT]TCTGCAGCCAGCTTT | 7464 |
rs760365247 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192272 | GTGCAGACAGTGCTC[A/G]TGAGGGCAGCGAGCC | 7464 |
rs760369899 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183116 | CTCAGGCCCTTCCCC[A/G]GCCTGGCGCCCCTCT | 7464 |
rs760401995 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182533 | ATTTCTGAGCTGGCA[C/T]TGTGGAGATTCTGTT | 7464 |
rs760470652 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140809 | CCTCTGGAAATACTC[-/T]TGGCTAATCCAGGTC | 7464 |
rs760519157 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170027 | CAAGCCCTGGACCCC[-/T]ATTTGTCTCTGTGCC | 7464 |
rs760527176 | snp | A/T | 1.68741e-05 | 0.00290461 | intron-variant | CORO2A | GRCh38.p7 | 9:98134986 | GGGCCCAAGGCAGCA[A/T]TAGCCAGGGCACCTT | 7464 |
rs760556724 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193957 | GCAGGTAGACTGAAC[A/G]CATGCTTCTGGTGTT | 7464 |
rs760579031 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145826 | CAAGTGATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 7464 |
rs760592181 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166114 | GTATGTAACTGTGCA[C/T]ACAGAGTATGGAGAA | 7464 |
rs760613369 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138808 | AATCCCAGCACTTTG[C/G]GGGGCCGAGGCGGGT | 7464 |
rs760635615 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122554 | TATTGACCACTGAAC[C/T]TTAGAGTAGGGCTCG | 7464 |
rs760636423 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | CORO2A | GRCh38.p7 | 9:98128235 | CCTGCTGTTGGAGGG[C/T]ATATGTCCTCTTGGT | 7464 |
rs760690885 | snp | C/T | 3.3184e-05 | 0.00407319 | intron-variant | CORO2A | GRCh38.p7 | 9:98128167 | CTTCTCTGCCTTCCT[C/T]ACCTCGATTCATCCC | 7464 |
rs760717615 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156891 | CCCCTTCAGGTGTTC[C/T]GCCTTAAGGTAGAGA | 7464 |
rs760758008 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185120 | TCCAAATCACACTAA[C/T]AACCCAGCTCAGGCA | 7464 |
rs760782519 | snp | A/C | 2.1906e-05 | 0.00330946 | stop-gained | CORO2A | GRCh38.p7 | 9:98124812 | GCAAGTTTTTGATCT[A/C]CAGTTCCAACTGTTT | 7464 |
rs760813591 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131387 | CTGGAGTGCAGTGGT[A/G]CGATCATAGCTCACT | 7464 |
rs760858560 | in-del | -/TCAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153691 | CACACACACACACAC[-/TCAC]ACTCACACACACACC | 7464 |
rs760862825 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168314 | TCCTATCTGCCACTC[G/T]GGGCAAGTTACTTAA | 7464 |
rs760955757 | snp | C/G/T | 3.29811e-05 | 0.00406075 | missense | CORO2A | GRCh38.p7 | 9:98128693 | TCTCGCAGGAGGACA[C/G/T]GTCGAGTCCTCTCTT | 7464 |
rs761059217 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188904 | ACATAAAGCACTTAG[A/G]ACAGAATTAGGCAGG | 7464 |
rs761073418 | snp | A/G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142221 | TGTGGCAGGCATTGC[A/G/T]AATGGATCCCAGCAC | 7464 |
rs761127333 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180164 | CTCCCTGCCCTTGGC[A/G]TCTGGCAAATACCTT | 7464 |
rs761155115 | snp | C/T | 1.68346e-05 | 0.00290121 | intron-variant | CORO2A | GRCh38.p7 | 9:98133261 | CAGGGGCCACCTTGC[C/T]CCTGGGCCTCATAGT | 7464 |
rs761220143 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129990 | CCTGGCTTTTTTTGA[C/T]GATCGGCAAACCCAT | 7464 |
rs761312861 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134778 | GAACTTGTTGGGGCT[A/G]CCCCAGAGAAAGAAT | 7464 |
rs761325931 | snp | C/G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156721 | GCTGACTCTCACTCA[C/G/T]GGTGGTGTACATGCT | 7464 |
rs761354979 | snp | A/G | 3.35289e-05 | 0.0040943 | intron-variant | CORO2A | GRCh38.p7 | 9:98126847 | GAAGCAGAGCCATGT[A/G]AGGACGGGGTGCCCA | 7464 |
rs761409495 | snp | G/T | 3.29506e-05 | 0.00405884 | missense | CORO2A | GRCh38.p7 | 9:98126730 | AAGAGCCGGGGTGAG[G/T]CTGGGGCCATGGAAT | 7464 |
rs761531666 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142701 | GAAGGCGCCTTAGGG[-/T]TGGGCGTGGCTCAGA | 7464 |
rs761578290 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164126 | GTGCCTGGTGAGAGG[G/T]TCTGAACCACCACAC | 7464 |
rs761618756 | in-del | -/G | 3.29783e-05 | 0.00406055 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98157525 | CAACTGCAATGAAGT[-/G]GGGGTTCACGGCACA | 7464 |
rs761624130 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123406 | CATACTAGCCCAACA[C/T]ATAAAATAGAAGGGA | 7464 |
rs761650890 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183268 | GTCACAATGCTACTG[C/T]GCTTGCAGCCACCCA | 7464 |
rs761675795 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158194 | CTCATGCCTGTAATC[C/T]CAGCATTTTGGGAGG | 7464 |
rs761759905 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128826 | GAGACCAGTCTCCTC[C/G]CAGAAAACAGCTCAG | 7464 |
rs761768570 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138045 | AGCTCTTTTGGAAAA[G/T]AGTCTGGCAGTTCCT | 7464 |
rs761796305 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184904 | ACAATGAATAATGAA[C/T]AGGTAGGTGCCTGGC | 7464 |
rs761886218 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148086 | ACCTCGCCTCTATTA[-/AAA]AAAAAAAAGAAAAAA | 7464 |
rs761887176 | snp | A/G | 0.000179678 | 0.00947665 | intron-variant | CORO2A | GRCh38.p7 | 9:98124926 | GAAGAAAGATCGGAA[A/G]GCAGGATCACCATGG | 7464 |
rs761955339 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151404 | CATTTTCCTTCTAAG[C/T]GTTGCTTGTTTATTC | 7464 |
rs761990264 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185269 | GGCCATGGGCCCTCA[C/T]GGCTGTGATGGGTCT | 7464 |
rs761993325 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164963 | CCACCACCAGGGTCT[-/A]GGTGTAACAATTCTT | 7464 |
rs762009345 | snp | C/T | 1.69189e-05 | 0.00290846 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157655 | GTACTGGGGGTGCCA[C/T]GACATCTGCAGGAGA | 7464 |
rs762123342 | in-del | -/GG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143728 | GCTCAGTATGTTTCA[-/GG]GGCCAGGGGATATAC | 7464 |
rs762171571 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155438 | TGCAACCTCTGCCTC[C/T]TGCGTTCAAGCAATT | 7464 |
rs762181812 | snp | A/C | 1.6577e-05 | 0.00287893 | missense | CORO2A | GRCh38.p7 | 9:98128719 | CTCTTTGGCATGACA[A/C]CTGAAGGCAGACAGG | 7464 |
rs762188291 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150611 | TATTTTCTTTATATC[A/C]GTTGTTAGTACCCAT | 7464 |
rs762266399 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170857 | TGCCCTGCCCACCTG[C/T]TAGGACGGTCTGTGG | 7464 |
rs762280002 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170427 | GCTGGTCAGGCTGGA[G/T]AATCCTAATTCTTTT | 7464 |
rs762368061 | snp | A/G | 1.69812e-05 | 0.00291382 | missense | CORO2A | GRCh38.p7 | 9:98134846 | AGGATGTTGGCGGCC[A/G]TGGGGTGCCACTCCA | 7464 |
rs762399724 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190631 | CAGCTCAGACATTCC[A/C]TGATTCCATGGTGCA | 7464 |
rs762423347 | snp | C/T | 1.69571e-05 | 0.00291174 | intron-variant | CORO2A | GRCh38.p7 | 9:98133269 | ACCTTGCCCCTGGGC[C/T]TCATAGTTACATGCT | 7464 |
rs762452703 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181485 | CTGGCTCCAAACATC[C/T]GTTAAACTTGGTCAT | 7464 |
rs762461559 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124641 | TGGAATCTCTTTCAG[C/T]GATGGAGAGTTTTGT | 7464 |
rs762582181 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156698 | CTAAGTCTGCTATTT[C/G]TGTTTCAGCTGACTC | 7464 |
rs762630120 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159121 | CTGGAGTGCAGTGGT[A/G]TGATCATAGCTCGCT | 7464 |
rs762652995 | snp | A/C | 1.70688e-05 | 0.00292132 | intron-variant | CORO2A | GRCh38.p7 | 9:98126861 | TGAGGACGGGGTGCC[A/C]ACGGGAAGATGGGCA | 7464 |
rs762701249 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136272 | TCCCTGGGGACAGGG[A/C]CAATTCTCACAGGAC | 7464 |
rs762710277 | snp | A/G | 1.65258e-05 | 0.00287448 | stop-gained | CORO2A | GRCh38.p7 | 9:98132220 | GCCGGTTGTTCCATC[A/G]GGATGTGCCTGTGGA | 7464 |
rs762739578 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155535 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 7464 |
rs762806224 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147838 | ATGTACACAAATGTT[A/T]GTAACAGCTTAATCT | 7464 |
rs762909482 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127692 | GGTGGCACGTGCCTG[C/T]AGTCCCAGCTACTCA | 7464 |
rs762911010 | snp | G/T | 3.61004e-05 | 0.0042484 | intron-variant | CORO2A | GRCh38.p7 | 9:98131092 | GCAGGGAAGGCCTGG[G/T]TCACTCCTGGGGGCC | 7464 |
rs762919017 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184512 | CTCTTTCTCTTACCG[G/T]GACATGGTGGCCCTC | 7464 |
rs762960985 | in-del | -/G | 1.65408e-05 | 0.00287578 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98134917 | TAGGCCGTGAGGTTC[-/G]CTGGTCAGCAGCTGC | 7464 |
rs762995358 | snp | A/C | 1.65616e-05 | 0.00287759 | missense | CORO2A | GRCh38.p7 | 9:98128254 | TGTCCTCTTGGTAGG[A/C]TTCTGACTGCAGGAG | 7464 |
rs762997392 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | CORO2A | GRCh38.p7 | 9:98137712 | CAGTGCCCAGGAGGG[C/T]TGGGGAGGAGGTGGA | 7464 |
rs763005119 | in-del | -/AGA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157940 | TGAATATAACAAGGC[-/AGA]AGAACCATAGAGAGA | 7464 |
rs763069852 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133134 | GTTGAAGGACATGGA[A/G]AGGATCACATCTTGG | 7464 |
rs763082082 | in-del | -/TA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144862 | TGGAGTCTACTCACC[-/TA]CTGCCCAGGGTGCAA | 7464 |
rs763094880 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170687 | GACCTCAGGTATCTG[-/C]CCACCTTGGCCTCCC | 7464 |
rs763119059 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121964 | AGCCCCAGTGACTGA[A/G]TAAATGGAGAATAAG | 7464 |
rs763123468 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | CORO2A | GRCh38.p7 | 9:98133069 | GCTCGGGGGTCAATA[A/G]CCCGAATCTTGCGGT | 7464 |
rs763131602 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164868 | GAGGGGTTCCAGGGA[-/G]GCAGGACTTACAGCG | 7464 |
rs763176546 | snp | C/T | 1.70603e-05 | 0.0029206 | intron-variant | CORO2A | GRCh38.p7 | 9:98157664 | GTGCCATGACATCTG[C/T]AGGAGACAAATGGGA | 7464 |
rs763199291 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151615 | TATATGTAAATAATA[A/G]CAGTTTTATTTCTTC | 7464 |
rs763208995 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166474 | CCATATGATAAGGTG[C/T]TAATGTTGAGAATAT | 7464 |
rs763227837 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176225 | TTATCAACCCATGAG[C/T]GTTGATTTAGAATCT | 7464 |
rs763310719 | in-del | -/GTACCT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138718 | TAATGCATCCCCCTG[-/GTACCT]GGTATCTGGAACCCT | 7464 |
rs763310871 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145006 | GAGATGAGAGGAGCA[C/T]TTCTTGACCCTAGGA | 7464 |
rs763373485 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157592 | GGAGTCGTAGCAGTT[C/T]TCCTTGCTGGCTGGT | 7464 |
rs763394226 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162031 | GTCATGGTTTTTGAG[C/T]GCTTACAAGCTGCCA | 7464 |
rs763433631 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132549 | CAAACTTCTGCCCAG[C/T]GCCCTGTTCTTGCTG | 7464 |
rs763453183 | snp | C/T | 1.73782e-05 | 0.00294767 | intron-variant | CORO2A | GRCh38.p7 | 9:98126507 | TGTTCCCCTCCACCC[C/T]AGCTGCCCCATGTGA | 7464 |
rs763456174 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162867 | AGCAGGCACTTGCCC[A/G]CAAGTGAGTACTGTA | 7464 |
rs763508368 | snp | C/G/T | 0.000131838 | 0.00811807 | missense | CORO2A | GRCh38.p7 | 9:98129866 | TGTCGGCGCTCACCT[C/G/T]GTAGTAGCGGATGTT | 7464 |
rs763568159 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171572 | AGCCAGCGCTGCAAG[C/T]TGCAGCAGGGAGATG | 7464 |
rs763627799 | in-del | -/AAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148085 | GACCTCGCCTCTATT[-/AAAA]AAAAAAAAGAAAAAA | 7464 |
rs763637282 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154206 | CACAGAATGAGGAAA[A/G]AAGTTGTTCATCTTT | 7464 |
rs763660607 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153289 | TGTTTTTAGTAGAGA[C/T]GGAGTTTCACCATGT | 7464 |
rs763675863 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173070 | AGCACTTTAGGAGGC[C/T]GAGGTGGGAGGATCG | 7464 |
rs763711137 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188916 | TAGGACAGAATTAGG[C/T]AGGCGGTAAACCCTC | 7464 |
rs763752585 | snp | A/G | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194000 | TTGGGTATCAAGCAT[A/G]TGGATGGCTGGGCGC | 7464 |
rs763772613 | snp | A/G | 1.89292e-05 | 0.0030764 | splice-donor-variant | CORO2A | GRCh38.p7 | 9:98130953 | TCCCGTGCCAAGCCG[A/G]CCTTCCCCACCACGT | 7464 |
rs763825169 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133808 | GCCCAGGCTGCAGTA[C/G]AGTGGCATGATCATG | 7464 |
rs763826178 | snp | C/G | 1.65693e-05 | 0.00287826 | intron-variant | CORO2A | GRCh38.p7 | 9:98129907 | TGAGGAGGAGGAGAA[C/G]GAAGAGGAGGGTGAG | 7464 |
rs763838813 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162192 | CTCAGCTGTCTCAAG[C/T]CTGCAGCTTTTGAGC | 7464 |
rs763917621 | in-del | -/AAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148095 | CTATTAAAAAAAAAA[-/AAG]AAAAAAAAAAAAAGA | 7464 |
rs763957506 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147004 | AGGTGTGGTGGCTCA[A/T]GCCTGTTATCCCAGC | 7464 |
rs763966105 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182548 | TTGTGGAGATTCTGT[C/T]CTTCCCAAGGGCCAG | 7464 |
rs763967937 | in-del | -/G | 1.67379e-05 | 0.00289287 | intron-variant | CORO2A | GRCh38.p7 | 9:98128295 | GTGAGGAGGGTGGTA[-/G]GGGTAGGCTGCTCAG | 7464 |
rs764046443 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181571 | AGCAGACCCCTCGGC[A/G]GCCATTGTTCTACTT | 7464 |
rs764076490 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191037 | CAAAGAGCTCACTAC[C/G]TGTCCAGGGGCCTCC | 7464 |
rs764133483 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181821 | GGCTCCCCTCACATC[A/G]TGTTTTCATCTCCAA | 7464 |
rs764166285 | in-del | -/A | 1.65411e-05 | 0.00287581 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98134918 | AGGCCGTGAGGTTCC[-/A]TGGTCAGCAGCTGCT | 7464 |
rs764198654 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175095 | CTATTCTTTTAGCCC[C/T]TCCTGACCCTTGACC | 7464 |
rs764219217 | snp | C/T | 1.6528e-05 | 0.00287467 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132257 | CTTCTTCAGGTTCCC[C/T]AGAAACAGCACTTTG | 7464 |
rs764275502 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | CORO2A | GRCh38.p7 | 9:98137731 | GGAGGAGGTGGATTC[C/T]ACATTAGCATCTGGA | 7464 |
rs764276251 | snp | A/C | 2.20929e-05 | 0.00332354 | missense | CORO2A | GRCh38.p7 | 9:98124814 | AAGTTTTTGATCTCC[A/C]GTTCCAACTGTTTGG | 7464 |
rs764329316 | snp | A/G | 8.108e-05 | 0.00636659 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124728 | TCTAAACCTCCCCAT[A/G]GAGCCGAGTGGTGTC | 7464 |
rs764331116 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134400 | GAACAGGGTTCCCCC[-/C]AAAACTCATGTCCAC | 7464 |
rs764341252 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147002 | CCAGGTGTGGTGGCT[C/T]ATGCCTGTTATCCCA | 7464 |
rs764380817 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160370 | TAGGTGTGCGGCCAG[A/G]TCCACCACACAGAGG | 7464 |
rs764481613 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129509 | TGGTAACTGCTTAAC[A/C]TTGACCTAGAACACA | 7464 |
rs764531975 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168322 | GCCACTCTGGGCAAG[G/T]TACTTAATGTGTCTA | 7464 |
rs764581272 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184232 | AAATTATTTTATTTT[-/A]TTTTTTTTTTTAATA | 7464 |
rs764616059 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189507 | ACCTGCCTCTAAGGG[C/G]ATTCATTTAATGAAT | 7464 |
rs764618283 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169534 | AACTCTGGCCCTGCA[C/T]TTTCCCTTAAAATGC | 7464 |
rs764639485 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179671 | GGGAGGTGAGCAGTC[A/G]GCCGGGCGCAGACAC | 7464 |
rs764655582 | snp | A/G | 4.94629e-05 | 0.00497283 | missense | CORO2A | GRCh38.p7 | 9:98128612 | CTGCCCTTACCCGCC[A/G]GGGCACAATCATGGA | 7464 |
rs764668209 | in-del | -/G | 1.74004e-05 | 0.00294956 | intron-variant | CORO2A | GRCh38.p7 | 9:98126864 | GGACGGGGTGCCCAC[-/G]GGAAGATGGGCATAT | 7464 |
rs764707566 | snp | A/G | 6.58989e-05 | 0.00573978 | missense | CORO2A | GRCh38.p7 | 9:98133162 | TGGTGACAGCTAATC[A/G]TACTCATGGGGCTTG | 7464 |
rs764708213 | in-del | -/TCT | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187722 | CTCAAAAGCCCCACC[-/TCT]TAATACCATCACCTT | 7464 |
rs764789729 | snp | A/G | 1.64874e-05 | 0.00287113 | intron-variant | CORO2A | GRCh38.p7 | 9:98134759 | ATTGTATTCCAGTTT[A/G]TGGGAACTTGTTGGG | 7464 |
rs764819089 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174767 | TGATTGTAAGTTTCC[C/T]GAGGCTCCCCAGCCA | 7464 |
rs764841971 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180224 | AGACCCTACGTTCAT[C/T]GCATCCCATATAGGC | 7464 |
rs764852384 | snp | A/G | 1.68117e-05 | 0.00289923 | intron-variant | CORO2A | GRCh38.p7 | 9:98126850 | GCAGAGCCATGTGAG[A/G]ACGGGGTGCCCACGG | 7464 |
rs764870924 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189067 | AATCTCTCAATTATA[A/G]TAAGGAGCACACCGC | 7464 |
rs764890547 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134018 | CAGCCTCTCAAACTG[C/T]TGGGATTACAGGTGT | 7464 |
rs764950745 | snp | C/T | 9.88338e-05 | 0.00702902 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126624 | TTTCTTCTCCTCCAG[C/T]CTGTGTTCTGCTGCC | 7464 |
rs765054716 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154547 | AGATGCTTTCCAGTC[A/G]TAACCCTCTCCATCC | 7464 |
rs765063815 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173316 | CCCAGCTCTATGATT[C/T]ACAACTATCGCTCAG | 7464 |
rs765083472 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134785 | TTGGGGCTGCCCCAG[A/C]GAAAGAATACCCAGA | 7464 |
rs765125581 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147239 | ACATGAATTAGGAAT[C/T]AGGTGACACAAGAGT | 7464 |
rs765128828 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122655 | ACTACTTCTTTACCT[C/T]GTATAGTCATTTCAG | 7464 |
rs765134365 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137617 | AAAATCATCAAAAGG[A/G]TTCCACTTGACATCC | 7464 |
rs765171079 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | CORO2A | GRCh38.p7 | 9:98133060 | ACGGTCCCTGCTCGG[A/G]GGTCAATAACCCGAA | 7464 |
rs765218282 | snp | A/G | 3.29603e-05 | 0.00405944 | intron-variant | CORO2A | GRCh38.p7 | 9:98137707 | CAAGACAGTGCCCAG[A/G]AGGGTTGGGGAGGAG | 7464 |
rs765266145 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156051 | GCTCTTTGTTTGAAT[-/T]TTTTTTTTTTTTTTT | 7464 |
rs765299966 | snp | C/G | 1.65795e-05 | 0.00287914 | splice-donor-variant | CORO2A | GRCh38.p7 | 9:98128169 | TCTCTGCCTTCCTCA[C/G]CTCGATTCATCCCGC | 7464 |
rs765356751 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136499 | TCTTAGCTAAACTAG[C/T]AGCTTAGCTGCTGCA | 7464 |
rs765439187 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98187928 | GTTTCAATAAGCCAT[A/G]TAACTTTTCTGTATT | 7464 |
rs765457925 | snp | A/G | 2.66294e-05 | 0.00364883 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124834 | CAACTGTTTGGCCTG[A/G]ACCTCTCGCTGGGTC | 7464 |
rs765475253 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175203 | ACTCCTGGCTATTCA[A/G]GGCCATCTCTGCCAG | 7464 |
rs765476284 | snp | C/T | 1.64972e-05 | 0.00287199 | missense | CORO2A | GRCh38.p7 | 9:98157513 | CACACTCAGTCACAA[C/T]TGCAATGAAGTGGGG | 7464 |
rs765523235 | snp | G/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186216 | CAGATGCTGAGCAAG[G/T]CCCCATCTCTTATTG | 7464 |
rs765566556 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185270 | GCCATGGGCCCTCAC[A/G]GCTGTGATGGGTCTA | 7464 |
rs765623365 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154003 | ATGATGATTTATCTT[C/T]ATAGATTTACTAATA | 7464 |
rs765641804 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160504 | GTTGCTAAGGAGCAG[C/T]ACATCTTTTCTCTAT | 7464 |
rs765720701 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130745 | CATCTGGGCCTGGAG[C/T]TGGGAAGAGACAAGG | 7464 |
rs765758376 | snp | A/G/T | 0.000201747 | 0.0100416 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124736 | TCCCCATGGAGCCGA[A/G/T]TGGTGTCCCTGAGGG | 7464 |
rs765766191 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170590 | GGGATTACAGGTGTG[A/C]ACCACCACGCCTGGC | 7464 |
rs765766286 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161013 | AGGAACCATGTGTAG[A/C]AGAGCACTTTCTTCT | 7464 |
rs765810203 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131696 | TTTATTTTAATAGAT[C/G]AAGAAGGAGACTCAG | 7464 |
rs765823502 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant | CORO2A | GRCh38.p7 | 9:98129790 | TTCAGTGTCCCTCAC[C/T]TACCGATCCCCTTCT | 7464 |
rs765858434 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168536 | CTAGTTAGTGGCTGG[C/G]CTGGAATCTGAAGCC | 7464 |
rs765862971 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134705 | CAACACCTTGATTTT[C/T]GATTTCTGGTCTCCA | 7464 |
rs765882359 | snp | A/G | 1.67598e-05 | 0.00289476 | intron-variant | CORO2A | GRCh38.p7 | 9:98128733 | ACCTGAAGGCAGACA[A/G]GGAGGGCCAAGAGGT | 7464 |
rs765884180 | snp | C/T | 1.68162e-05 | 0.00289962 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134857 | GGCCGTGGGGTGCCA[C/T]TCCACCAGGCCTACT | 7464 |
rs765917546 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171098 | GCGACAAGGATCACT[A/G]GGGATTTTCCAAGAC | 7464 |
rs765933563 | snp | C/G/T | 4.94338e-05 | 0.00497141 | missense | CORO2A | GRCh38.p7 | 9:98129794 | GTGTCCCTCACTTAC[C/G/T]GATCCCCTTCTGTGG | 7464 |
rs765953010 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190730 | ATCAGGCCAAAAAGG[C/T]TTGAATTAGGCAAGC | 7464 |
rs766004019 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132503 | CCCACTATCTTTGTT[-/AA]AAGAGTTATTTTTCT | 7464 |
rs766045280 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123556 | GCTGCAGTGCAGTCC[A/G]CAATCGTGGCTCATA | 7464 |
rs766098889 | in-del | -/TCTG | 6.58892e-05 | 0.00573936 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98126703 | TCTGCAGCCAGCTTT[-/TCTG]TCTGATTCAAGAGCC | 7464 |
rs766106947 | snp | C/G | 2.42545e-05 | 0.00348233 | intron-variant | CORO2A | GRCh38.p7 | 9:98134786 | TGGGGCTGCCCCAGA[C/G]AAAGAATACCCAGAC | 7464 |
rs766119816 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136286 | GCCAATTCTCACAGG[A/G]CCTGATTGTCCCTTT | 7464 |
rs766171086 | snp | C/T | | | splice-donor-variant | CORO2A | GRCh38.p7 | 9:98157459 | CTGGGGGTGTCCTTA[C/T]CTGGTGCAGGGGGAT | 7464 |
rs766214882 | snp | A/G | 1.64928e-05 | 0.00287161 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126765 | GATAGGTCTCTCTGC[A/G]GGCAGTGGGTGGGGT | 7464 |
rs766244552 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189671 | ACGGATCGGCCCAAG[C/G]TCACACAGTAGGGAA | 7464 |
rs766332072 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165148 | ATTTTTTTGTAAAGA[C/T]AGGGTTTCACTCTGT | 7464 |
rs766388195 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166253 | AAGAGCTAAATCTAT[-/A]AAAAAACCTTAGAAG | 7464 |
rs766409614 | snp | A/G | 1.65225e-05 | 0.00287419 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132221 | CCGGTTGTTCCATCG[A/G]GATGTGCCTGTGGAC | 7464 |
rs766411910 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167431 | AATACCACTGAACTG[C/T]ACACTTAAGAATGAT | 7464 |
rs766462636 | snp | G/T | 0.000116209 | 0.00762173 | missense | CORO2A | GRCh38.p7 | 9:98157471 | TTACCTGGTGCAGGG[G/T]GATGACGAGGAAGGC | 7464 |
rs766472696 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193117 | CCCGAGCAGTTACAG[C/T]GGTTACCGAGGCTTC | 7464 |
rs766576384 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128920 | TCACCTTCAAAGATT[A/T]AAATTATTTTAGCTG | 7464 |
rs766591614 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162049 | TTACAAGCTGCCAGG[C/T]GCCATTCCAAATGCT | 7464 |
rs766605170 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163386 | GTAGAGACAGGGTTT[C/T]GCCAAGTTGCCCAGG | 7464 |
rs766614555 | snp | C/T | 1.65751e-05 | 0.00287876 | missense | CORO2A | GRCh38.p7 | 9:98128257 | CCTCTTGGTAGGATT[C/T]TGACTGCAGGAGAAA | 7464 |
rs766615060 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182620 | GAAGTGGAATCTAAT[A/T]AGACCAGGTTCAAAG | 7464 |
rs766629831 | snp | C/T | 6.59109e-05 | 0.0057403 | missense | CORO2A | GRCh38.p7 | 9:98133072 | CGGGGGTCAATAACC[C/T]GAATCTTGCGGTCTT | 7464 |
rs766684762 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139283 | ACTATACACCTTAAA[A/G]CGGTGAATTTTCCAA | 7464 |
rs766691672 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176264 | AATTCTTCAGTTTTT[A/G]GCCAGACCCACTAAT | 7464 |
rs766716257 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151663 | TTTCAACTTTTCTTT[C/T]GCTATTTTTCTTTTT | 7464 |
rs766872431 | snp | A/C/G/T | 0.000102331 | 0.00715245 | intron-variant | CORO2A | GRCh38.p7 | 9:98126534 | GTGAAAGGCCCACCC[A/C/G/T]GTCCTCCTTCACACC | 7464 |
rs766914686 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138074 | CTCAAAAGGTTAACC[A/G]GTTCCCACATGACCC | 7464 |
rs766935268 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151336 | ATCCATGAATATAGT[A/G]AATATTTCCATCTAT | 7464 |
rs766946049 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120572 | ATTCCAGTTGCCCCC[C/T]CAGGCTCAAGTCTAG | 7464 |
rs766971775 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126530 | CCATGTGAAAGGCCC[A/C]CCCCGTCCTCCTTCA | 7464 |
rs766992834 | snp | A/C | 3.94151e-05 | 0.00443914 | intron-variant | CORO2A | GRCh38.p7 | 9:98130946 | ACCTCCCTCCCGTGC[A/C]AAGCCGACCTTCCCC | 7464 |
rs767052367 | in-del | -/AAAT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139629 | GAGACTCCGTCTCAA[-/AAAT]AAATAAATAAATAAA | 7464 |
rs767071198 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162108 | CTACCTTGCTCCCCC[A/G]TTCAGATGTAGGTGT | 7464 |
rs767073237 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98192098 | CCCACCCCACCGTTT[C/T]CTGTACCAGGAAGCT | 7464 |
rs767153618 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133702 | CCCCATACAAACAGA[C/T]GAGAAAGCGCTGTGG | 7464 |
rs767191835 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171171 | ACTGTCCGCTTTCTG[A/G]CACAGAGCTTTCAGA | 7464 |
rs767200303 | snp | A/G | 1.671e-05 | 0.00289045 | intron-variant | CORO2A | GRCh38.p7 | 9:98134963 | ATCTTAATCTGGCAG[A/G]GGAGACAGGGCCCAA | 7464 |
rs767222367 | in-del | -/GGA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144650 | CAGAGAAGGCTCCCT[-/GGA]GGAGGAGGACTTTAA | 7464 |
rs767226229 | in-del | -/ACGGAGTCGT | 1.64792e-05 | 0.00287042 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98157575 | CTGCGGGTGATAGGC[-/ACGGAGTCGT]AGCAGTTCTCCTTGC | 7464 |
rs767323750 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98132138 | TGAATGAATGACACT[A/G]GCTCTCAGCTGAGGG | 7464 |
rs767340362 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190900 | GTGGTCCAGCTCCCA[C/G]TCCTGTGCAGCTCCA | 7464 |
rs767346766 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137709 | AGACAGTGCCCAGGA[C/G]GGTTGGGGAGGAGGT | 7464 |
rs767371180 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189836 | TCAAATGAAATGTTT[A/G]TTAAGCCTCAGATAA | 7464 |
rs767399181 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181663 | AAGTCCTGTTTCCTC[C/T]AGCCGGAGGGCTTTG | 7464 |
rs767413864 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156836 | TTCATGTCAGTTTCT[C/G]CTGTGAGCCAGTGGC | 7464 |
rs767548306 | snp | G/T | 1.66776e-05 | 0.00288765 | intron-variant | CORO2A | GRCh38.p7 | 9:98128151 | ACATTTGCCTGGGCC[G/T]CTTCTCTGCCTTCCT | 7464 |
rs767575095 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159420 | CCTTTGGCTTGGCAT[C/T]CAAGGCCTCTGGCTG | 7464 |
rs767601325 | snp | A/T | 1.78634e-05 | 0.00298854 | intron-variant | CORO2A | GRCh38.p7 | 9:98126878 | CGGGAAGATGGGCAT[A/T]TGGGGCACCAATGAC | 7464 |
rs767656630 | snp | G/T | 1.64855e-05 | 0.00287097 | intron-variant | CORO2A | GRCh38.p7 | 9:98137720 | AGGAGGGTTGGGGAG[G/T]AGGTGGATTCCACAT | 7464 |
rs767724746 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153212 | TCAAGTGATTCTCCT[A/G]CCTCAGACTCCTGAG | 7464 |
rs767729590 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98194332 | GATGAAATCAGAACA[C/T]TGTGGGAATTCTTTA | 7464 |
rs767760132 | snp | C/T | 4.94825e-05 | 0.00497381 | missense | CORO2A | GRCh38.p7 | 9:98128608 | CCGACTGCCCTTACC[C/T]GCCGGGGCACAATCA | 7464 |
rs767775877 | snp | A/C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140963 | ACAACATTAAACTTA[A/C/T]ATAAGTTGATAATGT | 7464 |
rs767804257 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168310 | CATTTCCTATCTGCC[A/T]CTCTGGGCAAGTTAC | 7464 |
rs767814895 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167572 | ACAGTTCAGAAGAGA[C/G]TTAAGAGATCAGAGG | 7464 |
rs767852355 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127437 | CCGTGTTGGCAGGAG[C/T]GGGAGAGTGGCTCAG | 7464 |
rs767870141 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139521 | AATCCAAGCTACTTG[G/T]GAGACTGAGGCAGGA | 7464 |
rs767894629 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187535 | AGGAGGATGGAAGTC[C/G]AAGACTAAGACAGCA | 7464 |
rs767938199 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156353 | CTCTAACTTCTTAGA[C/T]GGAATGTTTAATCAT | 7464 |
rs768068374 | snp | A/C | 1.64751e-05 | 0.00287007 | missense | CORO2A | GRCh38.p7 | 9:98133085 | CCCGAATCTTGCGGT[A/C]TTTGCAGGTGGTGGC | 7464 |
rs768090337 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186720 | GTATGTACCCTATAG[A/G]TTGTTATGGGGATTG | 7464 |
rs768144073 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173906 | CAGATCACCTGAGAT[C/G]GGGAGTTCGAGACTA | 7464 |
rs768232544 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | CORO2A | GRCh38.p7 | 9:98137678 | GGGTAGTGGGGGTCC[A/G]ACTTCCCTGTCTGCA | 7464 |
rs768279766 | in-del | -/CT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151695 | TGAGACGGAATTTTG[-/CT]CTGTCACCCAGGCTG | 7464 |
rs768281667 | snp | C/T | 3.94625e-05 | 0.00444181 | missense | CORO2A | GRCh38.p7 | 9:98131036 | GTCCAGGTCCTCCTC[C/T]ATCAGAGGCACAGAG | 7464 |
rs768292805 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135845 | CACGAGAGTAGTGAC[A/G]GGCTCCAGATACTTC | 7464 |
rs768318413 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164772 | AGGGTAATTTTTCCT[C/T]CCTCCTTCAAAGCAA | 7464 |
rs768340320 | snp | A/G | 3.53207e-05 | 0.00420227 | intron-variant | CORO2A | GRCh38.p7 | 9:98157430 | CTGCCCTGCCTCCAG[A/G]GAGCTGTTTGGGCCT | 7464 |
rs768344837 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159065 | ATATCACCCTTTATT[A/T]ATTATTATTTTTGAG | 7464 |
rs768372194 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145108 | TTATGAGCACCCAGA[A/T]GAGCCTTTGGAGGGT | 7464 |
rs768406146 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128667 | TGTGATCAGCTTGTA[A/G]AAGCGGAAGATCTCG | 7464 |
rs768432846 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125191 | GGGGATTGGTGTTTT[C/T]GCCACCACTGAACTG | 7464 |
rs768466126 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134677 | TAGGGCATCTGGAGG[G/T]AGCTGGCTCTCCCAA | 7464 |
rs768610950 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183216 | CTCCAACCCTCTGTT[A/G]CTACTGATGTGGTAG | 7464 |
rs768618360 | snp | C/T | 3.30759e-05 | 0.00406655 | intron-variant | CORO2A | GRCh38.p7 | 9:98128593 | GCCTCCCATGCGGTC[C/T]CGACTGCCCTTACCC | 7464 |
rs768671425 | snp | C/G | 1.64738e-05 | 0.00286995 | missense | CORO2A | GRCh38.p7 | 9:98133126 | CCGTTGGTGTTGAAG[C/G]ACATGGAGAGGATCA | 7464 |
rs768700799 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140526 | ATTCACTGTAGCCTC[A/G]AACTCGGGGTAAGAC | 7464 |
rs768714743 | in-del | -/CTTAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137429 | TGTCTCCTCCTCTAC[-/CTTAA]CTTAACACCTCCCCA | 7464 |
rs768735284 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129855 | CAGGTGAGGCTTGTC[A/G]GCGCTCACCTCGTAG | 7464 |
rs768766704 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185855 | GGCTAGAAGCCAGGG[C/T]TGCATCCCTGGCAGC | 7464 |
rs768789913 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127818 | GCGAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 7464 |
rs768809381 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160938 | GACTCTCGTCCTTGG[C/T]CAAAGGGATGAGAAG | 7464 |
rs768810686 | snp | C/T | 8.26194e-05 | 0.00642673 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132206 | CCACAAGGCCACCTG[C/T]CGGTTGTTCCATCGG | 7464 |
rs768843608 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180171 | CCCTTGGCGTCTGGC[A/T]AATACCTTATACTCT | 7464 |
rs768863058 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144957 | GATGTGGGACCAGGG[A/C]CCGCCCAGAGGAGGC | 7464 |
rs768920647 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131400 | GTGCGATCATAGCTC[A/G]CTGCAGTCTCAAACT | 7464 |
rs768949334 | snp | A/G/T | 4.94607e-05 | 0.00497276 | intron-variant | CORO2A | GRCh38.p7 | 9:98129771 | TGGGATTACAGGCAT[A/G/T]AACTTCAGTGTCCCT | 7464 |
rs769000953 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157112 | CAATGTTTGTTTCCC[-/T]TTTTTTGGTGGGGAA | 7464 |
rs769002659 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190257 | CTTAGGATAAAGTCC[C/G]CAAAGTAGCCGGCTA | 7464 |
rs769022503 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143475 | GCAGAGGTGAAGTGG[A/G]CAGGCAGACTCTGGC | 7464 |
rs769024490 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156350 | CGGCTCTAACTTCTT[A/G]GATGGAATGTTTAAT | 7464 |
rs769027826 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170213 | CTCTTCCTTCCTCCC[A/C]CACCAACACACCCAT | 7464 |
rs769029793 | snp | A/G | | | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134911 | CTTCCTGTAGGCCGT[A/G]AGGTTCCTGGTCAGC | 7464 |
rs769071611 | in-del | -/GAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150430 | CATTCCCACTCAGGG[-/GAA]GAATGTTTGCATGTT | 7464 |
rs769095996 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161846 | GCCCTGGCCCCTTCC[A/G]GACCCTCTGAGCTGT | 7464 |
rs769098076 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134298 | AGGGCCTACTGCCTG[C/T]ATGCTTGATTGTCAG | 7464 |
rs769119864 | in-del | -/AGACGGTCCC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191250 | CACTCCGGACCTCTC[-/AGACGGTCCC]CAGGAGGGGCAGGAA | 7464 |
rs769122721 | snp | C/T | 8.29153e-05 | 0.00643823 | intron-variant | CORO2A | GRCh38.p7 | 9:98126961 | TGGGAAATACAGCTA[C/T]CTGTGGACAGGCCCA | 7464 |
rs769175510 | in-del | -/AAAT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139632 | CTCCGTCTCAAAAAT[-/AAAT]AAATAAATAAATAAA | 7464 |
rs769281439 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124173 | CGCCTGCCACCACGC[C/T]CAGCTAATTTTTTTG | 7464 |
rs769343638 | in-del | -/AA | 1.65482e-05 | 0.00287643 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98134909 | CCTTCCTGTAGGCCG[-/AA]TGAGGTTCCTGGTCA | 7464 |
rs769365163 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175632 | TCTGAGGAAGAATGG[A/G]TGCAGAGGGGCTGGT | 7464 |
rs769370715 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124636 | CCCACTGGAATCTCT[C/T]TCAGCGATGGAGAGT | 7464 |
rs769419928 | snp | A/G | 1.70953e-05 | 0.00292359 | intron-variant | CORO2A | GRCh38.p7 | 9:98157446 | GAGCTGTTTGGGCCT[A/G]GGGGTGTCCTTACCT | 7464 |
rs769422936 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150347 | CCCAATCTGACCTCA[A/C]CTCCTCCCACCACTC | 7464 |
rs769466845 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145539 | ATGGAGGGAACAGAT[A/G]TGTGCTATGGAAGGC | 7464 |
rs769489966 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165515 | GGGCTCGGAGGGGTC[A/G]GAGATGAATAATTCA | 7464 |
rs769527528 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138704 | TTGCCTGAGCACATT[A/C]ATGCATCCCCCTGGT | 7464 |
rs769529604 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148204 | GTTTGAGACCAGCCT[A/G]GCCAACATAGCAAAA | 7464 |
rs769534600 | snp | C/T | 1.98845e-05 | 0.00315307 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124780 | GGTCTCTGCTCAGAG[C/T]TGCTCTGAGCCCATC | 7464 |
rs769553412 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165951 | AGTGGTGTAATGGAT[-/G]GGTTGGCAATACCTG | 7464 |
rs769579567 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160715 | CACCTTGAGCAACTG[C/G]TGGGGGTGGCGGGAG | 7464 |
rs769596566 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174825 | TTTCCTTTATAAATT[A/G]CCCAGTCTCAGGTAT | 7464 |
rs769677505 | in-del | -/TTCC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125247 | CACTCTGAGCTTCCA[-/TTCC]TTCCTCTGGAAAATG | 7464 |
rs769683654 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98159219 | ACATGCCACCATACC[C/T]GGCTAATTAAAAAAA | 7464 |
rs769710429 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162582 | CTACCTCTCCCTTTG[C/T]ATGTGGCATGGAAGT | 7464 |
rs769746541 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186862 | GGCCTGGACCCCAAC[C/T]TCTCCCCTAGCACTG | 7464 |
rs769844745 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167105 | CAAGATCCTGTCTCA[-/AAAAAAAAAAAAAAA]GAAAGAAAAGAAAAA | 7464 |
rs769845275 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130161 | GTGCAATCACAGCTC[A/G]TTGCAACCTCCTGGT | 7464 |
rs769878882 | snp | G/T | 1.6522e-05 | 0.00287414 | missense | CORO2A | GRCh38.p7 | 9:98126571 | TCTGTCTTTGGTGGG[G/T]GGCATTCGAAAACGT | 7464 |
rs769888973 | snp | C/T | | | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172652 | ACATGGAGATAAATG[C/T]CTCTGCTCACCCTTA | 7464 |
rs769898149 | snp | A/T | 4.57017e-05 | 0.00478004 | missense | CORO2A | GRCh38.p7 | 9:98131056 | GAGGCACAGAGAGGT[A/T]ATCCTGCAGGGGAAG | 7464 |
rs769924488 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177227 | ACGATGTGAGGGGAA[A/C]CCTGGAGCACATTCA | 7464 |
rs769983588 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170900 | CTTGCACACACCAGA[C/T]ACACACAGGACCACA | 7464 |
rs769996354 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152981 | GTTGTATATTATAAT[C/T]AGCATTGAATCAATG | 7464 |
rs769999348 | snp | A/G | 8.47407e-05 | 0.0065087 | missense | CORO2A | GRCh38.p7 | 9:98157657 | ACTGGGGGTGCCATG[A/G]CATCTGCAGGAGACA | 7464 |
rs770006512 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142262 | ACCTCAGACTTGGGG[-/A]AATCCAGCATGGAGT | 7464 |
rs770013939 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144961 | TGGGACCAGGGACCG[C/T]CCAGAGGAGGCTGGG | 7464 |
rs770080740 | snp | C/G | 9.37339e-05 | 0.0068453 | intron-variant | CORO2A | GRCh38.p7 | 9:98124940 | AGGCAGGATCACCAT[C/G]GTGTCAGGACACCAG | 7464 |
rs770129123 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127144 | TCCCACCCACACTGC[A/C]CCCCACCATCTACCA | 7464 |
rs770217947 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | CORO2A | GRCh38.p7 | 9:98137548 | TCTTCAGGAAGGGGA[A/G]GCCCCTCAGGGGCTG | 7464 |
rs770220176 | snp | A/G | 0.000131817 | 0.00811735 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129858 | GTGAGGCTTGTCGGC[A/G]CTCACCTCGTAGTAG | 7464 |
rs770221304 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181464 | TATAGGCGTGAGCCT[C/T]GGTGCCTGGCTCCAA | 7464 |
rs770298492 | snp | C/G | 3.30447e-05 | 0.00406464 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128186 | TCGATTCATCCCGCT[C/G]AGCCACTCCTGGGCC | 7464 |
rs770344891 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164633 | GAATCTAAGGCCAGA[C/T]CCTGGTTTAAACCAC | 7464 |
rs770388791 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193644 | TAACAGAGTACACTG[C/T]TACTACTTTACATAT | 7464 |
rs770420138 | snp | C/G | 1.65658e-05 | 0.00287795 | missense | CORO2A | GRCh38.p7 | 9:98134936 | GTCAGCAGCTGCTTG[C/G]GGATGCTCCAGATCT | 7464 |
rs770489090 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126287 | GATCTGCCCGCCTTG[C/G]CCTCCCAAAGTGCTG | 7464 |
rs770490031 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137836 | CTTCTTATTCCCTGT[-/G]GGATCCTGGGGGAGT | 7464 |
rs770513543 | snp | C/T | 3.35835e-05 | 0.00409764 | intron-variant | CORO2A | GRCh38.p7 | 9:98128130 | TGGGCACGCCATGTT[C/T]CTGTCACATTTGCCT | 7464 |
rs770526589 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166840 | ATAATATTCAACCTT[C/T]AAAAGGAAGAAAACT | 7464 |
rs770569932 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138520 | AAGAATGGACATACA[A/G]AATGCAGTATATTCA | 7464 |
rs770578660 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO2A | GRCh38.p7 | 9:98185719 | CACGCCATAGACCAC[A/G]CCCTGTGCAAGAACT | 7464 |
rs770593745 | snp | C/T | 3.30246e-05 | 0.0040634 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128201 | GAGCCACTCCTGGGC[C/T]GTCAGGGAGGGCTGG | 7464 |
rs770602320 | in-del | -/ACACAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153650 | CTTCTCTGTTTCCAA[-/ACACAC]ACACACACACACACA | 7464 |
rs770646488 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151235 | TCAAAGTAGTCAGGG[C/T]ATGGTTCTAAGGAAA | 7464 |
rs770686346 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165744 | CGCATGTTAGGAGCA[A/G]GGATAACAGAAACAC | 7464 |
rs770687005 | snp | C/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122565 | GAACTTTAGAGTAGG[C/G]CTCGGAACACAGATT | 7464 |
rs770699393 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175669 | ATTACACAACACAAT[C/T]GCATGGAGAGGCAGC | 7464 |
rs770704205 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98174941 | ATGGTTAAAATCGTA[A/G]ACTTTGCTATGTATA | 7464 |
rs770729468 | snp | C/T | | | missense | CORO2A | GRCh38.p7 | 9:98137607 | AGGCGATCTCAAAAT[C/T]ATCAAAAGGGTTCCA | 7464 |
rs770735431 | snp | C/T | 3.30841e-05 | 0.00406706 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133038 | TGGCCCAGAACTGAC[C/T]TGGAGGACGGTCCCT | 7464 |
rs770777441 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135815 | ATCTTGGATTTAAAA[-/C]CAGGAAGCCAACCCC | 7464 |
rs770788426 | snp | A/G | 1.66441e-05 | 0.00288474 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98157634 | ATGACGGAACTTGGA[A/G]CTCCGGTACTGGGGG | 7464 |
rs770799057 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148430 | ATAAATAAATAAATA[A/C]AAATTTAAAAAAAGA | 7464 |
rs770935921 | snp | C/G | 3.31521e-05 | 0.00407123 | intron-variant | CORO2A | GRCh38.p7 | 9:98133226 | TCATCACCTGCATGG[C/G]AGAGAGCCAGCTCTG | 7464 |
rs770980840 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98166519 | CAACTCAACAACAAG[A/C]AAGCAAACAATTTGA | 7464 |
rs770982762 | snp | A/G | 9.88647e-05 | 0.00703012 | missense | CORO2A | GRCh38.p7 | 9:98157564 | TGTCGTGAACGCTGC[A/G]GGTGATAGGCACGGA | 7464 |
rs771034871 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163469 | TGCTGAGATTACAGG[C/T]GTAAGCCATTGTGCC | 7464 |
rs771055941 | in-del | -/CA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164147 | CCACCACACTTATGT[-/CA]CACAGCCACAGTTAG | 7464 |
rs771069393 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187461 | GAAACTCCATCTCAA[-/A]AAAAAAAAAAAAAAA | 7464 |
rs771079098 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122888 | GGGACAGCATCTATC[C/T]ATATCAGGCTGATTC | 7464 |
rs771090863 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140772 | TAGTAGCTCTGCAAA[C/T]AGAGGAGGTGGTCCT | 7464 |
rs771128379 | snp | G/T | 1.64735e-05 | 0.00286993 | missense | CORO2A | GRCh38.p7 | 9:98133146 | GGAGAGGATCACATC[G/T]TGGTGACAGCTAATC | 7464 |
rs771161864 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153081 | ATTTGGGGGTAAAGG[A/G]TCATCTCTATAACTT | 7464 |
rs771189766 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177615 | GGGATTACAGGCATG[C/T]GCCACCACACCCGGC | 7464 |
rs771222085 | snp | A/G | | | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172845 | AGTGCCAGCAGCCTG[A/G]GTTTATGAGGATTAA | 7464 |
rs771224646 | in-del | -/G | 1.64741e-05 | 0.00286998 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98133151 | GGATCACATCTTGGT[-/G]ACAGCTAATCGTACT | 7464 |
rs771228062 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128491 | GCTGTGAGAAAGGCC[A/G]CTCTGTGGCTGCCCC | 7464 |
rs771303832 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122071 | CACTGAACCCCCATC[A/G]TGCTGCAGCTGCGGT | 7464 |
rs771311674 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188590 | GCCAACATGGCGAAA[C/T]ACCGTCTCTACTGAA | 7464 |
rs771327097 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146735 | CCCAGGTCTGGGCTC[C/T]CATTCGGGTCCTGGA | 7464 |
rs771352018 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134371 | CATCCACTCCGGGCA[G/T]GCTATAATGAGTTGA | 7464 |
rs771377811 | snp | A/G | 1.64969e-05 | 0.00287196 | intron-variant | CORO2A | GRCh38.p7 | 9:98137560 | GGAAGCCCCTCAGGG[A/G]CTGACACTCACTGTG | 7464 |
rs771378299 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133580 | TGCACAGGCTGTGCA[C/T]GCAGAGGTCCAGGGC | 7464 |
rs771390898 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162739 | CGTGTGCATCCCTTT[C/G]GATGTTTAACTGAGG | 7464 |
rs771405269 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174322 | GGAGATGTTCATTCA[C/T]ATAAAGTGCCTCAGA | 7464 |
rs771450078 | snp | A/G | 4.94189e-05 | 0.00497062 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137653 | GTTGCCTCTGTGCCC[A/G]CAGACTTTTGGGTAG | 7464 |
rs771460842 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187390 | CTTGAACCCGGGAGA[C/T]GGTGGCTGCAGTGAG | 7464 |
rs771489458 | snp | C/T | 6.59424e-05 | 0.00574168 | missense | CORO2A | GRCh38.p7 | 9:98126584 | GGGGGCATTCGAAAA[C/T]GTCAAAGCCATTTGT | 7464 |
rs771508436 | snp | C/T | 6.58924e-05 | 0.0057395 | missense | CORO2A | GRCh38.p7 | 9:98137669 | CAGACTTTTGGGTAG[C/T]GGGGGTCCAACTTCC | 7464 |
rs771547506 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183911 | GTTTGCAGTGAGCTG[A/G]GATTGTGCCACTACA | 7464 |
rs771554325 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183080 | CACCCTGGATCTCCA[C/G]AGCTTCACGGAATTT | 7464 |
rs771572729 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158911 | AGCCAGAGGGGCGAG[A/G]AGAGCCAGATCACAA | 7464 |
rs771637175 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172930 | GACTGGCTGTGAGGA[C/T]AGGTGACAGCATCAC | 7464 |
rs771645535 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128512 | TGGCTGCCCCATGAA[C/T]GTGGGCTCCAGGCTC | 7464 |
rs771697593 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140349 | GTCTTGGGATTTTTT[C/T]TAGAGGGACTTTCAA | 7464 |
rs771786893 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139949 | CCCATGCCACACAGC[A/C]CTGAAGCTATTTCCA | 7464 |
rs771869570 | snp | C/T | 1.65971e-05 | 0.00288067 | intron-variant | CORO2A | GRCh38.p7 | 9:98128582 | GTTCCCCACCTGCCT[C/T]CCATGCGGTCCCGAC | 7464 |
rs771883835 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162398 | TCCCCACTTCCCCAC[A/G]GATGAAGCCAGCTGA | 7464 |
rs771924987 | snp | A/G | 3.30213e-05 | 0.00406319 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128206 | ACTCCTGGGCCGTCA[A/G]GGAGGGCTGGGCCCC | 7464 |
rs771924996 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | CORO2A | GRCh38.p7 | 9:98133115 | CCAACAGGCTGCCGT[C/T]GGTGTTGAAGGACAT | 7464 |
rs771973660 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182835 | CAGCTTTTTACATTT[C/T]AACATCTCTGAAACT | 7464 |
rs771977617 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121311 | TCAACAGAAAGGGGA[C/T]GCCCAGGGTATGGAA | 7464 |
rs771980876 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169215 | CCCCGCCCCCGCGCC[A/G]CCCATCCTTCTGGTC | 7464 |
rs772017084 | snp | A/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187096 | CATCCTGGCTAACAC[A/T]GTGAAACCCCGTCTC | 7464 |
rs772069174 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131145 | AGAATTGCTGCCATG[C/G]TGCTCTGGGCGAGAG | 7464 |
rs772072299 | snp | G/T | 0.000148389 | 0.00861234 | intron-variant | CORO2A | GRCh38.p7 | 9:98129766 | AGTGCTGGGATTACA[G/T]GCATGAACTTCAGTG | 7464 |
rs772109870 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160175 | GAGCTACAGGAAGCT[A/G]CACAGAATGTAGGGA | 7464 |
rs772159243 | in-del | -/ATATATATATATATATATATAC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154352 | TATATATATATATAT[-/ATATATATATATATATATATAC]ACACAAATACATATA | 7464 |
rs772211317 | in-del | -/AC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153652 | TCTCTGTTTCCAAAC[-/AC]ACACACACACACACA | 7464 |
rs772219999 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126210 | CGGCTAATTTTTGTA[-/T]TTTTTAGTAGAGATG | 7464 |
rs772251586 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170392 | CAAGGGGCTGGGCCC[A/G]TCACTGTCATAGCAG | 7464 |
rs772266826 | snp | C/T | 6.59217e-05 | 0.00574078 | missense | CORO2A | GRCh38.p7 | 9:98128681 | AGAAGCGGAAGATCT[C/T]GCAGGAGGACACGTC | 7464 |
rs772352459 | in-del | -/CTC | 3.29476e-05 | 0.00405866 | cds-indel | CORO2A | GRCh38.p7 | 9:98126615 | CAGCCAGGTTTTCTT[-/CTC]CTCCAGCCTGTGTTC | 7464 |
rs772375768 | snp | A/G | 1.66832e-05 | 0.00288814 | intron-variant | CORO2A | GRCh38.p7 | 9:98133248 | CCAGCTCTGAGCACA[A/G]GGGCCACCTTGCCCC | 7464 |
rs772379953 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163892 | GAACCCAAACTGGGC[A/G]TGGTGCAAACCATTA | 7464 |
rs772417626 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160336 | AAAGAGATCACCTGA[A/T]ACGCAGGAGGAGTTA | 7464 |
rs772431830 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154172 | TTGTCTGGTTTTGGT[A/G]TCAAGGTTACAGTGG | 7464 |
rs772434336 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98126714 | CTTTTCTGTCTGATT[C/T]AAGAGCCGGGGTGAG | 7464 |
rs772434505 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173777 | TTCTCTAAGTCTTGA[G/T]ACCACATCGTCAGGT | 7464 |
rs772446815 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98180118 | CGTCAGTGCTAAAAC[A/G]CTCCTCCCTGACAGG | 7464 |
rs772467519 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130202 | CTTCCCGCCTCAGCC[C/T]CCCGAGTAGGTGGGA | 7464 |
rs772507255 | snp | G/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123134 | CAGGACTTGCAAGAG[G/T]TCACTGAGTAAGCTG | 7464 |
rs772537315 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162800 | GTGTATCCGTGCATG[C/T]ATGACTTTAATGACT | 7464 |
rs772571878 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158563 | TGAGCCCAGCCTTTA[C/T]AGGAGTGAAGAGTCC | 7464 |
rs772604654 | snp | C/G | 1.65269e-05 | 0.00287457 | missense | CORO2A | GRCh38.p7 | 9:98132192 | GCCCTCACCTGGTCC[C/G]ACAAGGCCACCTGCC | 7464 |
rs772608209 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189495 | GGGGAGCTAGCTACC[C/T]GCCTCTAAGGGGATT | 7464 |
rs772619487 | in-del | -/G | 3.9152e-05 | 0.0044243 | intron-variant | CORO2A | GRCh38.p7 | 9:98131100 | GCCTGGGTCACTCCT[-/G]GGGGGCCCTCAGTGG | 7464 |
rs772664446 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130205 | CCCGCCTCAGCCTCC[C/T]GAGTAGGTGGGACCA | 7464 |
rs772706016 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134536 | TGCTCTCCTCTTCCT[A/G]TAAGGAAGACAGGTA | 7464 |
rs772761931 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172018 | TAAGTGGGTTTCATT[-/T]CATGTCCAGCTCCAG | 7464 |
rs772766989 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137391 | GAGGAGGGGTGGTGC[C/T]GCTAGTCCTACAGCA | 7464 |
rs772801781 | snp | A/G | 4.96964e-05 | 0.00498455 | intron-variant | CORO2A | GRCh38.p7 | 9:98132318 | TGGAGGGACACGTGC[A/G]GTCGGTATTGGAGAG | 7464 |
rs772826891 | snp | C/T | 0.000150914 | 0.0086853 | missense | CORO2A | GRCh38.p7 | 9:98134862 | TGGGGTGCCACTCCA[C/T]CAGGCCTACTCTGCG | 7464 |
rs772914866 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189663 | AGAGGGGAACGGATC[A/G]GCCCAAGGTCACACA | 7464 |
rs772976934 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169178 | GCAAATGCAAAGAGT[A/C]CCGTCCTCAGGTTTC | 7464 |
rs773028758 | snp | A/G | 1.65222e-05 | 0.00287417 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132209 | CAAGGCCACCTGCCG[A/G]TTGTTCCATCGGGAT | 7464 |
rs773104272 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136124 | CATCGGGGAAGGGGC[A/G]GTGGCAGGCAATGAG | 7464 |
rs773112432 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145627 | AGAACATTATCTGCA[C/G]GCAGCAAGGAGTCCT | 7464 |
rs773136280 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | CORO2A | GRCh38.p7 | 9:98133130 | TGGTGTTGAAGGACA[A/T]GGAGAGGATCACATC | 7464 |
rs773208010 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98187460 | CGAAACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 7464 |
rs773219528 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | CORO2A | GRCh38.p7 | 9:98137708 | AAGACAGTGCCCAGG[A/G]GGGTTGGGGAGGAGG | 7464 |
rs773262313 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161971 | CGTGAGAGGCCTGGG[C/T]AACACCTCCCCTGGA | 7464 |
rs773307499 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177386 | ACGCTTGATCACAAA[C/T]GTGGTGGCGTGTTAG | 7464 |
rs773309381 | snp | C/T | 1.65269e-05 | 0.00287457 | missense | CORO2A | GRCh38.p7 | 9:98128242 | TTGGAGGGTATATGT[C/T]CTCTTGGTAGGATTC | 7464 |
rs773362270 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133065 | CCCTGCTCGGGGGTC[A/G]ATAACCCGAATCTTG | 7464 |
rs773388951 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127677 | AAATTAGCTGGGCAT[A/G]GTGGCACGTGCCTGT | 7464 |
rs773410910 | snp | C/T | 3.47983e-05 | 0.00417109 | intron-variant | CORO2A | GRCh38.p7 | 9:98126502 | GGATCTGTTCCCCTC[C/T]ACCCCAGCTGCCCCA | 7464 |
rs773416667 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98153005 | ATCAATGTTAAATTT[C/G]TAGGATGTGGTTATA | 7464 |
rs773418672 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138962 | TGAGGCAGTAGAATC[A/G]CTTGAACCCAGGAGG | 7464 |
rs773436607 | in-del | -/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170278 | CTGTGCCCACCTACA[-/G]CCCTGTGGGTACCCA | 7464 |
rs773473821 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98140594 | AACTACAGGCATGTG[C/T]CACCAAGCTCAGCTA | 7464 |
rs773485827 | snp | A/G | | | missense | CORO2A | GRCh38.p7 | 9:98126581 | GTGGGGGGCATTCGA[A/G]AACGTCAAAGCCATT | 7464 |
rs773492754 | snp | C/T | | | utr-variant-5-prime, intron-variant | CORO2A | GRCh38.p7 | 9:98172732 | GGTACCTCCTCTCTG[C/T]TTCCAGCCTCCAGGA | 7464 |
rs773538432 | in-del | -/C | 1.65384e-05 | 0.00287557 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98132293 | CGGTGCCCTTTGTAG[-/C]CTGGCCTCCTGGAGG | 7464 |
rs773580579 | in-del | -/AT | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193594 | ACTGCTCCGTGGCAC[-/AT]ATAGTAACCACTCAA | 7464 |
rs773618810 | snp | C/T | 6.59837e-05 | 0.00574348 | missense | CORO2A | GRCh38.p7 | 9:98126578 | TTGGTGGGGGGCATT[C/T]GAAAACGTCAAAGCC | 7464 |
rs773628507 | in-del | -/AGGG | 6.58892e-05 | 0.00573936 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98126663 | ATCTTCTCCTCCAAC[-/AGGG]AGGGAGGAAGACCTC | 7464 |
rs773729183 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98129861 | AGGCTTGTCGGCGCT[C/T]ACCTCGTAGTAGCGG | 7464 |
rs773760403 | snp | A/G | 3.31505e-05 | 0.00407113 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134938 | CAGCAGCTGCTTGGG[A/G]ATGCTCCAGATCTTA | 7464 |
rs773769421 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182209 | TACATACAGAAAGTA[A/G]TCAATCGTGAACAAA | 7464 |
rs773779077 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171038 | CCCTGACCAAAACTC[C/T]ACACAGGTTTATTGC | 7464 |
rs773832994 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182311 | CTCCAGGATTATCTG[C/T]GTGGGGCAGATATCT | 7464 |
rs773883435 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | CORO2A | GRCh38.p7 | 9:98137566 | CCCTCAGGGGCTGAC[A/G]CTCACTGTGGCATCT | 7464 |
rs773923320 | snp | C/T | 4.96652e-05 | 0.00498298 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134929 | GTTCCTGGTCAGCAG[C/T]TGCTTGGGGATGCTC | 7464 |
rs774007218 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98165849 | AAATTCTCAAGCCTC[A/C]TTCCCCAGACCTACT | 7464 |
rs774051592 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146738 | AGGTCTGGGCTCCCA[C/T]TCGGGTCCTGGACAC | 7464 |
rs774164287 | snp | A/G | 1.67612e-05 | 0.00289488 | intron-variant | CORO2A | GRCh38.p7 | 9:98128136 | CGCCATGTTCCTGTC[A/G]CATTTGCCTGGGCCT | 7464 |
rs774193961 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138646 | GCACAAAAGGCCACA[C/T]GTTGTGTGATTCCAC | 7464 |
rs774230198 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181243 | GCCAGAACCCACGGG[A/C]ACCCACGTGGCCTCC | 7464 |
rs774307659 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | CORO2A | GRCh38.p7 | 9:98132325 | ACACGTGCGGTCGGT[A/G]TTGGAGAGACAGTAG | 7464 |
rs774336862 | snp | A/C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189025 | AAGCTCATAATCACA[A/C/T]CTTCCTTGTCCCCAC | 7464 |
rs774367894 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146297 | CCTCTCCCCAGCCTT[C/T]CCCTGCTGCCTTTGT | 7464 |
rs774419576 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142177 | AGACCAGGAATGGAG[A/C]CCACAGCTGCACTGT | 7464 |
rs774431378 | snp | C/G | 1.65853e-05 | 0.00287964 | intron-variant | CORO2A | GRCh38.p7 | 9:98133230 | CACCTGCATGGCAGA[C/G]AGCCAGCTCTGAGCA | 7464 |
rs774462196 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168259 | AAACAACATGCCCAT[A/C]TCTGAACAAAGTTCT | 7464 |
rs774503703 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129212 | AGCTGAACTTTTATA[A/G]GCAGTTTGCTCTGCT | 7464 |
rs774564698 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162775 | TATATACACATGCAT[A/G]AGCGCATGCGTGTAT | 7464 |
rs774619356 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188826 | ACAAAAGAAACAAAC[-/AA]AAAAACTAGTACAAT | 7464 |
rs774626906 | snp | G/T | 1.64743e-05 | 0.00287 | missense | CORO2A | GRCh38.p7 | 9:98133149 | GAGGATCACATCTTG[G/T]TGACAGCTAATCGTA | 7464 |
rs774628267 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155758 | TAAGGAGTTTGCCCA[C/T]ATTGTTAATGTTCTC | 7464 |
rs774648585 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122893 | AGCATCTATCCATAT[C/T]AGGCTGATTCTGGTT | 7464 |
rs774723683 | snp | G/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122081 | CCATCGTGCTGCAGC[G/T]GCGGTTCCCAGAGAT | 7464 |
rs774735821 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158376 | TTTAGACCCCTTGGT[A/G]CATGGCAGATACTTG | 7464 |
rs774802815 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171655 | TTCAAGGCCAAGTAG[A/C]GCAAGCCCAGCAGAG | 7464 |
rs774816361 | snp | A/C | 1.64727e-05 | 0.00286986 | missense | CORO2A | GRCh38.p7 | 9:98126692 | TCCAGCCATCTTCTG[A/C]AGCCAGCTTTTCTGT | 7464 |
rs774832445 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98172933 | TGGCTGTGAGGACAG[A/G]TGACAGCATCACATT | 7464 |
rs774881140 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183054 | ACAAGGGTCTATTGA[A/G]GCCTAGCATTCACCC | 7464 |
rs774949895 | snp | C/T | 7.54802e-05 | 0.00614284 | missense | CORO2A | GRCh38.p7 | 9:98131029 | AGGAGCCGTCCAGGT[C/T]CTCCTCCATCAGAGG | 7464 |
rs774956667 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133581 | GCACAGGCTGTGCAT[A/G]CAGAGGTCCAGGGCA | 7464 |
rs775078081 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147665 | AATATTTTAGCATAA[G/T]GAGGTTCCATGCAAT | 7464 |
rs775192024 | in-del | -/AA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170006 | GAAAAAGAAGGCACC[-/AA]AAGTTCAAGCCCTGG | 7464 |
rs775196583 | in-del | -/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142329 | AGAGCTGGGCTTGAG[-/C]CCAGGCCTCTGGTTC | 7464 |
rs775198564 | in-del | -/A | 1.65459e-05 | 0.00287622 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98134912 | TTCCTGTAGGCCGTG[-/A]GGTTCCTGGTCAGCA | 7464 |
rs775219322 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193851 | GAGCTGGACGGGCTC[C/T]CTGCCTACCACCCAA | 7464 |
rs775305518 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146825 | CAATGGGGCAAGATC[C/T]CCTATAAATGGGGCT | 7464 |
rs775326435 | in-del | -/GT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163711 | TGACATACATGCGGG[-/GT]GTGTGTGTGTGTGTG | 7464 |
rs775356242 | snp | A/G | 1.64849e-05 | 0.00287092 | stop-gained | CORO2A | GRCh38.p7 | 9:98133058 | GGACGGTCCCTGCTC[A/G]GGGGTCAATAACCCG | 7464 |
rs775365288 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176132 | CTAAACATTCGGCGG[G/T]GGGTGAGGGGTGTCA | 7464 |
rs775383090 | snp | G/T | 1.6574e-05 | 0.00287867 | intron-variant | CORO2A | GRCh38.p7 | 9:98128586 | CCCACCTGCCTCCCA[G/T]GCGGTCCCGACTGCC | 7464 |
rs775390938 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150378 | TGTGGTCACAGCACA[G/T]GTGTCCACGTGCTGA | 7464 |
rs775392558 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182841 | TTTACATTTTAACAT[C/T]TCTGAAACTGGGATG | 7464 |
rs775396754 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98157840 | TTACAGTTACTTCTG[C/T]AGACCTGGTAAGATA | 7464 |
rs775423169 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128525 | AACGTGGGCTCCAGG[C/T]TCTGGTGCCCGACAG | 7464 |
rs775434600 | snp | A/G | 3.30311e-05 | 0.0040638 | missense | CORO2A | GRCh38.p7 | 9:98128233 | CCCCTGCTGTTGGAG[A/G]GTATATGTCCTCTTG | 7464 |
rs775506302 | snp | C/T | 2.04606e-05 | 0.00319842 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98124798 | CTCTGAGCCCATCCG[C/T]AAGTTTTTGATCTCC | 7464 |
rs775558884 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181454 | GTGCTAGGATTATAG[G/T]CGTGAGCCTCGGTGC | 7464 |
rs775668978 | snp | G/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123847 | TTTAGTGGAGACGGG[G/T]TTTCACCATGTTGGC | 7464 |
rs775691582 | snp | C/T | 1.67668e-05 | 0.00289537 | intron-variant | CORO2A | GRCh38.p7 | 9:98133256 | GAGCACAGGGGCCAC[C/T]TTGCCCCTGGGCCTC | 7464 |
rs775706471 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170577 | CTCCCAAGTAGCTGG[G/T]ATTACAGGTGTGCAC | 7464 |
rs775753856 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | CORO2A | GRCh38.p7 | 9:98128686 | CGGAAGATCTCGCAG[A/G]AGGACACGTCGAGTC | 7464 |
rs775770996 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142220 | CTGTGGCAGGCATTG[C/T]GAATGGATCCCAGCA | 7464 |
rs775772775 | in-del | -/AT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127098 | ACACTTCAAACTCAC[-/AT]GAGACCTTGCCCTTG | 7464 |
rs775816470 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168354 | TTCCTCACCAGGAAA[A/C]TCAGGCACTACAAAT | 7464 |
rs775817507 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98143414 | CTCAGGGTGGAGACT[A/G]GGAGGCAGGGGTGGC | 7464 |
rs775869669 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169277 | AAGTACAGATTGAGT[C/T]AGAGAGCAAACCAAG | 7464 |
rs775975893 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179184 | CTCGCTGACATCTGC[A/G]GACTGGGAAGAAACC | 7464 |
rs775978351 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158639 | TACTATGGGTAATAA[C/G]AGAGATTCGCACATG | 7464 |
rs775990924 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163998 | GGATGGGTAGGCATT[C/G]CTGGCTACCAGTGCC | 7464 |
rs775993972 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164023 | AGTGCCCCTTCGTAA[A/G]TTTGTGGTTTCACAT | 7464 |
rs776036289 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123198 | ACTCTTTGGGCTGAG[A/G]ACTGCATCAGACCCA | 7464 |
rs776082882 | snp | A/T | 3.34571e-05 | 0.00408992 | intron-variant | CORO2A | GRCh38.p7 | 9:98126844 | AGGGAAGCAGAGCCA[A/T]GTGAGGACGGGGTGC | 7464 |
rs776167597 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149055 | TATCTTGACTGTAGT[A/G]ATGCCAGTATCACAA | 7464 |
rs776181410 | in-del | -/G | 4.95344e-05 | 0.00497642 | frameshift-variant | CORO2A | GRCh38.p7 | 9:98126722 | TCTGATTCAAGAGCC[-/G]GGGTGAGGCTGGGGC | 7464 |
rs776215006 | snp | C/T | 3.47766e-05 | 0.00416978 | intron-variant | CORO2A | GRCh38.p7 | 9:98157437 | GCCTCCAGAGAGCTG[C/T]TTGGGCCTGGGGGTG | 7464 |
rs776223777 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123380 | TTTTTTTTCCTAGCA[A/G]AATTGTTTTTCATAC | 7464 |
rs776248871 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164995 | TTTTTTTGAGATAGG[A/G]CCTCACTTTGCTACC | 7464 |
rs776291665 | in-del | -/TCATCACCTGCATGGCAGAGAGCCAGC | 1.65116e-05 | 0.00287324 | intron-variant | CORO2A | GRCh38.p7 | 9:98133211 | TATCCAGGTTCCAGA[-/TCATCACCTGCATGGCAGAGAGCCAGC]TCTGAGCACAGGGGC | 7464 |
rs776329312 | snp | A/G | 2.06755e-05 | 0.00321517 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98131041 | GGTCCTCCTCCATCA[A/G]AGGCACAGAGAGGTT | 7464 |
rs776338359 | snp | A/C | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124335 | GTTTCAAACTCCCGA[A/C]CTCAAGCAATCCGCC | 7464 |
rs776372425 | in-del | -/AGTA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178380 | TAGCATTATTAGCAT[-/AGTA]AGTAAGCACTGCTAA | 7464 |
rs776378278 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184083 | GTTACATGTAAACAC[C/T]ATACTATTTTATATC | 7464 |
rs776379064 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134729 | GTCTCCAGAACTGTG[A/T]CAGAATACATTTCCA | 7464 |
rs776431581 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145275 | AAATGTTTCCTACTT[C/T]GAGCCCAGTGTGGCC | 7464 |
rs776433494 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173936 | AGCCTGACCAACATG[C/G]AGAAACCCCGTCTTT | 7464 |
rs776462618 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | CORO2A | GRCh38.p7 | 9:98137687 | GGGTCCAACTTCCCT[A/G]TCTGCAAGACAGTGC | 7464 |
rs776463368 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128799 | GCCAGGCTGCACACC[C/T]GGACCTGAACAGAGA | 7464 |
rs776493594 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98128670 | GATCAGCTTGTAGAA[A/G]CGGAAGATCTCGCAG | 7464 |
rs776498913 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167397 | GTGGTGATGGCTGCA[C/T]GGCAGTATGAGCGTA | 7464 |
rs776550370 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98168155 | CAGCTCCTTAGTCAC[A/G]CTAGCAACATTTCAA | 7464 |
rs776566509 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158172 | CCATCTCAGCTAGGC[A/G]TGGCAGCTCATGCCT | 7464 |
rs776628383 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151298 | AATGCTGTGGGAATT[C/T]GAGGGAGGAAGTAAA | 7464 |
rs776771810 | snp | C/T | 2.41217e-05 | 0.00347279 | missense | CORO2A | GRCh38.p7 | 9:98124826 | TCCAGTTCCAACTGT[C/T]TGGCCTGGACCTCTC | 7464 |
rs776772839 | snp | A/G | 1.83333e-05 | 0.00302759 | intron-variant | CORO2A | GRCh38.p7 | 9:98124922 | TGGGGAAGAAAGATC[A/G]GAAGGCAGGATCACC | 7464 |
rs776815075 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98129632 | GTTGCACACGTCAAG[-/T]ACAGCCCCCACCAAG | 7464 |
rs776821766 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137896 | CCTCAGTAAAAGGGA[A/G]CAATCACAGGTATTT | 7464 |
rs776869525 | snp | C/T | 1.65217e-05 | 0.00287412 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98132242 | GCCTGTGGACATCAG[C/T]TTCTTCAGGTTCCCC | 7464 |
rs776906732 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98185163 | GGGAGCCTTCCATGA[C/T]CCCCCACTTCCACCC | 7464 |
rs777023080 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146226 | CACCTTCTTCACCCC[A/C]TCCCTGGAGTGACTC | 7464 |
rs777039222 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131428 | ACTCTTGGGCTCAAG[C/T]GATCCTCTCGCCTCA | 7464 |
rs777058522 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190356 | CACAGGCGAATCCCT[A/G]TAGCCTTGCCAGCAC | 7464 |
rs777083501 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170282 | GCCCACCTACAGCCC[C/T]GTGGGTACCCAGGGG | 7464 |
rs777103721 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169583 | CCTCAGGATAAAGTC[C/G]TCTGCTGGACTTGGG | 7464 |
rs777103772 | snp | A/G | 1.65433e-05 | 0.002876 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134914 | CCTGTAGGCCGTGAG[A/G]TTCCTGGTCAGCAGC | 7464 |
rs777105228 | snp | C/G | 3.29478e-05 | 0.00405867 | missense | CORO2A | GRCh38.p7 | 9:98133093 | TTGCGGTCTTTGCAG[C/G]TGGTGGCCAACAGGC | 7464 |
rs777106702 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98136816 | TAAATGGTGACAATG[A/C]CTTTTATCTTTATTT | 7464 |
rs777126655 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189565 | AGATTTGTTCACTCT[A/C]AGAGGTTGGCTGTCA | 7464 |
rs777131490 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134453 | TATTTGGAAATGGGG[A/T]CTTCGCTGCTGAAAT | 7464 |
rs777157125 | snp | C/T | 0.000221294 | 0.0105165 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134845 | GAGGATGTTGGCGGC[C/T]GTGGGGTGCCACTCC | 7464 |
rs777204941 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138333 | GGTAGAACACTTGAA[A/C]CTGGGAGGTGGAGGT | 7464 |
rs777211913 | snp | C/G | 3.37901e-05 | 0.00411022 | intron-variant | CORO2A | GRCh38.p7 | 9:98133265 | GGCCACCTTGCCCCT[C/G]GGCCTCATAGTTACA | 7464 |
rs777215718 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151879 | TGGAGTACAGTGGCG[C/T]GATCTCGACTCACTG | 7464 |
rs777290329 | snp | C/T | 1.65168e-05 | 0.00287369 | missense | CORO2A | GRCh38.p7 | 9:98128193 | ATCCCGCTGAGCCAC[C/T]CCTGGGCCGTCAGGG | 7464 |
rs777333961 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139729 | TGAGCCTGGGAGGTC[A/G]AGGCTGCAGTCAGCT | 7464 |
rs777343719 | snp | C/G | 1.65888e-05 | 0.00287996 | intron-variant | CORO2A | GRCh38.p7 | 9:98133030 | CCAGCCCCTGGCCCA[C/G]AACTGACCTGGAGGA | 7464 |
rs777383128 | snp | C/T | 1.66788e-05 | 0.00288775 | missense | CORO2A | GRCh38.p7 | 9:98124875 | GGAGCCTTCGGATCT[C/T]CTCCTGTTGCCGGTA | 7464 |
rs777405102 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127274 | TTATCCAAAACTAGG[A/G]CTCGGCCCTGGTCCG | 7464 |
rs777418961 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176584 | CTTAACTCAGGACCA[C/T]GGGATGGCTCCACTG | 7464 |
rs777434175 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151079 | TTTGCTTGTGCCCTT[C/T]CCTTTGCCATTTATA | 7464 |
rs777478696 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161505 | GTTGCAGCGAGCCAA[A/G]ATCGCACCACTGCAC | 7464 |
rs777495911 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149467 | TTTACAAAGAAAAGA[C/T]GTTTGTTTGGCTCAC | 7464 |
rs777499699 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186867 | GGACCCCAACCTCTC[C/T]CCTAGCACTGAGCTC | 7464 |
rs777504876 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169127 | TTGACCATCACCAGC[A/G]AGGCAGAAGCCGTCT | 7464 |
rs777557426 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120635 | AAGATCCTTGGTCTC[C/T]GCCCTGCCTATGCTC | 7464 |
rs777564131 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126035 | CTGGTCCCCACCATC[-/TT]TTTTTTTTTTTTTTT | 7464 |
rs777586151 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175644 | TGGATGCAGAGGGGC[C/T]GGTTTATTTATTACA | 7464 |
rs777631086 | snp | G/T | 4.96882e-05 | 0.00498414 | missense | CORO2A | GRCh38.p7 | 9:98157624 | TGCCAAAGACATGAC[G/T]GAACTTGGAGCTCCG | 7464 |
rs777664098 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131967 | CGGACTCCCCTGGGT[A/C]CTGACCCATCTCCCT | 7464 |
rs777668931 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135271 | TGGGCAGGTGGCTGG[C/G]TTTCAGGCCTGTCTC | 7464 |
rs777682469 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | CORO2A | GRCh38.p7 | 9:98157561 | GGTTGTCGTGAACGC[C/T]GCGGGTGATAGGCAC | 7464 |
rs777683103 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188519 | TCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGA | 7464 |
rs777684628 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188547 | AGACAAGCGGATCAT[C/T]TGAGGTCAGGAGTTC | 7464 |
rs777707829 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98163348 | GCGCATGCCACTGTG[A/C]CCCACTAATTTTTGT | 7464 |
rs777738857 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144778 | AGGAGGCTGAAGCAG[C/G]CAGCGGGCACGGTAG | 7464 |
rs777743903 | snp | A/G | 1.66123e-05 | 0.00288199 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134881 | GCCTACTCTGCGCGC[A/G]TGGCCCACGAGTTCC | 7464 |
rs777771845 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170211 | TTCTCTTCCTTCCTC[C/T]CCCACCAACACACCC | 7464 |
rs777776973 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122793 | CATCATCCTGCAGGA[A/G]GCAGGCTGTGTACCT | 7464 |
rs777839914 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123605 | GTTCAAGCAATTCTC[C/T]TATCTCAGCCTCCCG | 7464 |
rs777865427 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176907 | AGTCCAAAAGAGTAC[A/G]CTAAAACACAGAACA | 7464 |
rs777926680 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98183726 | GTATTTTGGGAGGCT[C/G]AGGCGGGCAGATTAC | 7464 |
rs777938587 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134320 | GATTGTCAGTGGAGC[A/T]GGGTCGGGGGAACGA | 7464 |
rs777943659 | snp | A/G | 1.65023e-05 | 0.00287244 | missense | CORO2A | GRCh38.p7 | 9:98126778 | GCAGGCAGTGGGTGG[A/G]GTCTCAGCAGCTCAG | 7464 |
rs777970377 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128403 | CAAAGGGACTTGCCC[A/G]AGGTCACGCAGCAGC | 7464 |
rs778057364 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158059 | AGCCAGCCTGCCTGG[A/G]TTTCAATCCCAGCTC | 7464 |
rs778082517 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182796 | TCTAATTGGGGACCC[A/G]CCACATGTCAAATGA | 7464 |
rs778106490 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152831 | TGACCTTTACTCCTG[-/A]AAAAATGTTAATATC | 7464 |
rs778132538 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158662 | CGCACATGACAGTCA[A/G]GGAGGGCTTCTCAAA | 7464 |
rs778156453 | in-del | -/GAGACCAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142160 | TCTTGAAGGGCTCTA[-/GAGACCAG]GAGACCAGGAATGGA | 7464 |
rs778190400 | snp | A/G | 5.22298e-05 | 0.00511001 | missense | CORO2A | GRCh38.p7 | 9:98130998 | TCCGCGTCATAGAAG[A/G]GAAACAGCACGCCCG | 7464 |
rs778191201 | snp | A/G | 1.67536e-05 | 0.00289423 | intron-variant | CORO2A | GRCh38.p7 | 9:98128298 | GAGGAGGGTGGTAGG[A/G]TAGGCTGCTCAGATG | 7464 |
rs778211201 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191550 | AGAGGCAGTGACTGG[A/G]TAGCAGATTCCAGCT | 7464 |
rs778257216 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147408 | GGTAAAAGGGATGAG[C/T]GAAGCAAGAGGGCAA | 7464 |
rs778313142 | snp | C/T | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98193522 | CTCCACTCCACACCA[C/T]GTCTGTGAAGAGCTC | 7464 |
rs778346131 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141470 | AATTCTCCCTGCCTC[A/G]GCCTCCTGAGTAGCT | 7464 |
rs778347853 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128473 | CCCACTGATGTCACA[C/T]TGGCTGTGAGAAAGG | 7464 |
rs778383118 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176722 | ATGGGGGCTGAGAAC[C/T]CCTCAGCAGAGCAGG | 7464 |
rs778401206 | snp | C/G/T | 3.29572e-05 | 0.00405928 | splice-donor-variant | CORO2A | GRCh38.p7 | 9:98129793 | AGTGTCCCTCACTTA[C/G/T]CGATCCCCTTCTGTG | 7464 |
rs778485288 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188120 | GAACATGCCAGGCAT[A/G]GTCCTGCCTCAGGGC | 7464 |
rs778507349 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139924 | TGGGAGGGACATACA[A/G]GTCCCCCAGCCCATG | 7464 |
rs778507867 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162416 | TGAAGCCAGCTGACA[C/G]CAAAAGAGCGTGAAC | 7464 |
rs778513387 | snp | C/T | 4.94385e-05 | 0.0049716 | missense | CORO2A | GRCh38.p7 | 9:98128624 | GCCGGGGCACAATCA[C/T]GGAGATGGGCTCGAT | 7464 |
rs778515159 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126036 | TGGTCCCCACCATCT[-/T]TTTTTTTTTTTTTTT | 7464 |
rs778570408 | snp | C/T | 6.59391e-05 | 0.00574153 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98133191 | TGTGATGACAGACTC[C/T]TTTGTATCCAGGTTC | 7464 |
rs778615436 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158907 | TACAAGCCAGAGGGG[C/T]GAGGAGAGCCAGATC | 7464 |
rs778631106 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98178454 | GTCCATTCTGTAAGC[A/G]CTAGTTAGCTTAGAG | 7464 |
rs778632567 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152555 | TCTCAAAGTGCTGGG[A/C]CCATAGGTGTGAGCC | 7464 |
rs778648400 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152462 | GCCTGGTTAATTTTT[A/G]CATTTTTTGTAGAGA | 7464 |
rs778702851 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151250 | CATGGTTCTAAGGAA[A/T]AAATAGGCTTGGAAT | 7464 |
rs778736602 | snp | A/G | | | | | GRCh38.p7 | 9:98149660 | ATTATCACAGGGAGG[A/G]CATCAAGCCATTCAT | 7464 |
rs778762457 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | CORO2A | GRCh38.p7 | 9:98133112 | TGGCCAACAGGCTGC[C/T]GTTGGTGTTGAAGGA | 7464 |
rs778811547 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98121205 | ACAATCTCAAGTTTT[A/G]TTTCAGGAAGCACAA | 7464 |
rs778820723 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125170 | GGATGCCTGGCTCTG[A/C]AGTCTGGGGATTGGT | 7464 |
rs778828472 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98169268 | GCCCACAGGAAGTAC[A/G]GATTGAGTCAGAGAG | 7464 |
rs778831054 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179962 | GAGCCGAGATCACGC[C/G]ACTGCACTCCAGCCT | 7464 |
rs778859534 | in-del | -/GGGGAAGGGGAGGC | 2.51373e-05 | 0.00354514 | intron-variant | CORO2A | GRCh38.p7 | 9:98131064 | AGAGGTTATCCTGCA[-/GGGGAAGGGGAGGC]GGGGAAGGGGAGGCA | 7464 |
rs778918442 | in-del | -/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123496 | CCTATTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 7464 |
rs778925165 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98133334 | GGGTGGCGCAGCTGG[A/C]AGCCTGGCCAAGAAG | 7464 |
rs778933666 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161671 | GCAGGTAAGAGGCAA[C/T]GGTCACCCGGGCTGG | 7464 |
rs778954317 | snp | A/G | 9.48114e-05 | 0.00688453 | intron-variant | CORO2A | GRCh38.p7 | 9:98130907 | AGGCTGCTGTCTGCC[A/G]CTGTCTCAGGGGTCC | 7464 |
rs779025692 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98138447 | TGGTTCACCAATGTT[C/G]ACAACAATATTCTTC | 7464 |
rs779049528 | snp | A/G | 1.65258e-05 | 0.00287448 | missense | CORO2A | GRCh38.p7 | 9:98132264 | AGGTTCCCCAGAAAC[A/G]GCACTTTGCTGGCCC | 7464 |
rs779108018 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98190044 | CATGTGCCACCACAC[A/C]CAGCTAATTTTTATA | 7464 |
rs779109509 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156146 | TCCCTGGGCTCAGGT[A/G]ATCTGACCTCAGCCT | 7464 |
rs779113318 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98161227 | CTCAGATACCCGGAC[G/T]CTGAGGGCAGTGGGG | 7464 |
rs779130226 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164520 | GCCTCTGGGTAACCA[C/T]TTCCCACAGCATCTT | 7464 |
rs779175958 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123753 | CTCCGCCTCCCAGGC[C/T]CAAGCGATTCTCCTG | 7464 |
rs779245732 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173708 | CAGTACACGTGCTTA[A/C]GATACGGGCTTCAGA | 7464 |
rs779271681 | snp | C/T | 3.3018e-05 | 0.00406299 | intron-variant | CORO2A | GRCh38.p7 | 9:98126925 | AGACACTCAGAGCCA[C/T]GCAGACCCATGCAAC | 7464 |
rs779336677 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189333 | GCAAGGCATGGATTA[C/T]AGACTTAAAACACAA | 7464 |
rs779347372 | snp | G/T | 1.70237e-05 | 0.00291746 | intron-variant | CORO2A | GRCh38.p7 | 9:98157345 | AATGACTTACTCAAG[G/T]TCACACAGCTAGTAA | 7464 |
rs779352676 | snp | C/G | 3.29462e-05 | 0.00405857 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98137656 | GCCTCTGTGCCCGCA[C/G]ACTTTTGGGTAGTGG | 7464 |
rs779363522 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148576 | AAAACCTCACCTCTA[A/C]ATAAAAAATATACAA | 7464 |
rs779506924 | snp | C/G | 3.88327e-05 | 0.00440623 | intron-variant | CORO2A | GRCh38.p7 | 9:98157388 | GGACTTTCTAGAAAC[C/G]CAGGCTCTTTCCACT | 7464 |
rs779541189 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130030 | GGGAACACCAGGAAA[C/G]TGGGGGCCCTGTCAT | 7464 |
rs779565380 | snp | A/G | 2.31613e-05 | 0.00340296 | intron-variant | CORO2A | GRCh38.p7 | 9:98130917 | CTGCCGCTGTCTCAG[A/G]GGTCCAGGAGGTCAC | 7464 |
rs779595690 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147544 | CCTTGCTATTGAAAA[C/T]GCAATTGGCAAACAA | 7464 |
rs779673077 | in-del | -/CAGACGGTCC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98191248 | TCACTCCGGACCTCT[-/CAGACGGTCC]CAGACGGTCCCCAGG | 7464 |
rs779675845 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167330 | TGAAAAGTTATTGTT[A/T]AATGGATATAGAGTT | 7464 |
rs779707976 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98127643 | ATGGCAAAACCCCCA[A/T]CTCTACTAAAAATAC | 7464 |
rs779709153 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189254 | CCACAGAAGCAAAGT[C/T]ACCTACTCCTGGCCC | 7464 |
rs779725363 | in-del | -/TCT | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98123495 | CCTATTCTCTCTCTC[-/TCT]TTTTTTTTTTTTTTT | 7464 |
rs779768747 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141854 | CTATGCATGAAGAGC[C/T]CAACAGTCAGGTGTT | 7464 |
rs779851447 | snp | A/G | 3.37861e-05 | 0.00410997 | intron-variant | CORO2A | GRCh38.p7 | 9:98128743 | AGACAGGGAGGGCCA[A/G]GAGGTTCTGGCTAGG | 7464 |
rs779869206 | snp | A/G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179832 | ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA | 7464 |
rs779898610 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | CORO2A | GRCh38.p7 | 9:98128636 | TCATGGAGATGGGCT[C/T]GATGAGGCTTTTGGT | 7464 |
rs779937556 | in-del | -/AAAACAAAACA/AAAACAAAACAAAACA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148770 | AAAACAAAACAAAAC[-/AAAACAAAACA/AAAACAAAACAAAACA]AAACAAACAAAAAAA | 7464 |
rs779940419 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144896 | TGGACCCAATAGAGA[G/T]GTGGACAAATGGATA | 7464 |
rs779954456 | snp | G/T | 0.000131813 | 0.00811721 | missense | CORO2A | GRCh38.p7 | 9:98129851 | AGCTCAGGTGAGGCT[G/T]GTCGGCGCTCACCTC | 7464 |
rs780010070 | snp | C/T | 1.65534e-05 | 0.00287688 | missense | CORO2A | GRCh38.p7 | 9:98134901 | CCACGAGTTCCTTCC[C/T]GTAGGCCGTGAGGTT | 7464 |
rs780017364 | snp | A/G | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98122723 | ATGTCTCCAGTGATG[A/G]GGGCCCCCTACCTCC | 7464 |
rs780031887 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176108 | CTCAAAGCGGCAATA[-/T]CAAAAGATCTAAACA | 7464 |
rs780082100 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | CORO2A | GRCh38.p7 | 9:98126646 | TCTGCTGCCCACCTT[A/G]GCATCTTCTCCTCCA | 7464 |
rs780182594 | snp | A/T | 1.65496e-05 | 0.00287655 | missense | CORO2A | GRCh38.p7 | 9:98128175 | CCTTCCTCACCTCGA[A/T]TCATCCCGCTGAGCC | 7464 |
rs780249658 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98145892 | TGATTTTTTATTTTT[A/G]GTAGAGACAGGGTTT | 7464 |
rs780251536 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141460 | AGGTTCAAGCAATTC[A/T]CCCTGCCTCGGCCTC | 7464 |
rs780280366 | in-del | -/AGG | 1.64811e-05 | 0.00287059 | cds-indel | CORO2A | GRCh38.p7 | 9:98128684 | AGCGGAAGATCTCGC[-/AGG]AGGACACGTCGAGTC | 7464 |
rs780289113 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156206 | CCTCATGCCCAGTTA[A/G]TTTTTGTATTTTTTG | 7464 |
rs780320653 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131332 | CTTAACAAATCACTT[-/T]TTTTTTTTTTTTTGA | 7464 |
rs780328226 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98171319 | TCCAACCAGGGGTCC[G/T]GCATTCTGTTCTCAG | 7464 |
rs780396357 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150166 | TCAAACTCCTGACCT[C/T]GTGATCTGCCTGCCT | 7464 |
rs780399475 | snp | A/G | 1.65334e-05 | 0.00287514 | missense | CORO2A | GRCh38.p7 | 9:98132280 | GCACTTTGCTGGCCC[A/G]GTGCCCTTTGTAGCT | 7464 |
rs780419270 | in-del | -/AAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167102 | AGCAAGATCCTGTCT[-/AAA]CAAAAAAAAAAAAAA | 7464 |
rs780428733 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174612 | TTGGATCATGGAGGC[G/T]GTTTCCCCCAGGCTG | 7464 |
rs780436308 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98181194 | GCGCGACTCCCTCTG[C/T]AAGTCAGGCCATGAG | 7464 |
rs780449804 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175306 | CAGGACATGCCTGGA[C/T]GATATTTCCCCAGGC | 7464 |
rs780510497 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125205 | TCGCCACCACTGAAC[-/T]GTGTGACCTTGGGCA | 7464 |
rs780529144 | snp | A/C | 1.6517e-05 | 0.00287372 | missense | CORO2A | GRCh38.p7 | 9:98157614 | CTGGCTGGTTTGCCA[A/C]AGACATGACGGAACT | 7464 |
rs780593212 | snp | A/T | 1.65258e-05 | 0.00287448 | missense | CORO2A | GRCh38.p7 | 9:98132193 | CCCTCACCTGGTCCC[A/T]CAAGGCCACCTGCCG | 7464 |
rs780595563 | snp | C/T | 3.29701e-05 | 0.00406005 | missense | CORO2A | GRCh38.p7 | 9:98157534 | TGAAGTGGGGGTTCA[C/T]GGCACAGAAGTGGTT | 7464 |
rs780624924 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150927 | TCACCCCAGCATTCA[A/G]GGCTCTGCTCAGCTA | 7464 |
rs780642392 | snp | C/T | 1.6557e-05 | 0.00287719 | intron-variant | CORO2A | GRCh38.p7 | 9:98132313 | CCTCCTGGAGGGACA[C/T]GTGCGGTCGGTATTG | 7464 |
rs780677774 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98135683 | TTGATCTTCCTTATT[G/T]GTCCTGCAAGGTTCT | 7464 |
rs780682941 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98150206 | AAAGTGCTGAGATTG[C/T]AGGTGTTAGCCACAG | 7464 |
rs780749628 | snp | G/T | 1.9856e-05 | 0.00315081 | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98124767 | TGAGGAGGGCAGAGG[G/T]CTCTGCTCAGAGCTG | 7464 |
rs780800995 | snp | C/T | 1.64974e-05 | 0.00287201 | intron-variant | CORO2A | GRCh38.p7 | 9:98129746 | CTCCCACCTCGGCCT[C/T]CCGAAGTGCTGGGAT | 7464 |
rs780811858 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98137298 | TTTTCCCATCGGAAT[A/G]TACATTTTCACTGGG | 7464 |
rs780841143 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174730 | GTGAAGAAGGTGCCA[G/T]CTTCCCCTTCACCTT | 7464 |
rs780872690 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131863 | GTACCTCATTTGCTC[C/G]AGGTGCACCCTCAGC | 7464 |
rs780894655 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98175448 | AGGGAGCCCTGCTCT[G/T]TGCAGGGAGGGCACA | 7464 |
rs780905414 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98167586 | ACTTAAGAGATCAGA[A/G]GCACAGCAAGAAGTG | 7464 |
rs780913387 | snp | A/G | 0.000479706 | 0.0154798 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98131009 | GAAGGGAAACAGCAC[A/G]CCCGAGGAGCCGTCC | 7464 |
rs780919251 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98128081 | TGAGAGAAGAAAAAT[C/G]CAGGCCCAACCCCTC | 7464 |
rs780973642 | snp | A/G | 3.65684e-05 | 0.00427585 | synonymous-codon | CORO2A | GRCh38.p7 | 9:98134815 | ACTCACCTTGTAGTC[A/G]TAGCCAGCACTGAAG | 7464 |
rs780979361 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98130108 | TCTTATTTTTTTGAG[A/G]CAGGGTCTCACTTTA | 7464 |
rs781002110 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98160066 | CAGCACCAGGTAGCA[C/T]GTCAGTCTTGCAGGG | 7464 |
rs781002566 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184795 | TGTCTGTCTCTGTCC[A/G]ATTTGATTGTAGCCC | 7464 |
rs781016403 | in-del | -/AACAACAAAA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98188783 | TCAGAAAACAACAAC[-/AACAACAAAA]AACAACAACAAAAAC | 7464 |
rs781016673 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98170159 | TCAGCCCATGGAAGC[A/G]CCCCTCGTCTCCTTT | 7464 |
rs781087223 | snp | A/G | 1.65345e-05 | 0.00287524 | missense | CORO2A | GRCh38.p7 | 9:98126568 | TTCTCTGTCTTTGGT[A/G]GGGGGCATTCGAAAA | 7464 |
rs781113876 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98172576 | CCCCACTTCTGAGCT[C/G]GACCCCACAGCGGGA | 7464 |
rs781138384 | snp | A/G | 2.26549e-05 | 0.00336555 | intron-variant | CORO2A | GRCh38.p7 | 9:98130924 | TGTCTCAGGGGTCCA[A/G]GAGGTCACCTCCCTC | 7464 |
rs781186762 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98147275 | TTAATGTGATCCTGG[A/C]ATTATGGTTATGTCA | 7464 |
rs781195650 | snp | C/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121470 | TAAAAATTACCTATC[C/T]CTCTCCCTTGCTGTG | 7464 |
rs781206498 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179874 | CAGGTGCGGTGGCAG[A/G]TGCCTGTAATCCCAG | 7464 |
rs781249547 | snp | A/G | 3.31038e-05 | 0.00406827 | intron-variant | CORO2A | GRCh38.p7 | 9:98133222 | CAGATCATCACCTGC[A/G]TGGCAGAGAGCCAGC | 7464 |
rs781309364 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98142083 | TAAAAACAAAAATAC[A/G]GATTTTCTGAAAAAA | 7464 |
rs781316243 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134278 | TACTGTGGGTCCCAA[C/T]CTACAGGGCCTACTG | 7464 |
rs781383093 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98155051 | CAGAAGTGTCTGATC[A/G]TTTACACAACTCTGT | 7464 |
rs781420764 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98146331 | CTGAGTACAGTCCCT[G/T]GTTGCCAAGGCTGCA | 7464 |
rs781422241 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98182096 | TCCTCCTCCAGATTC[C/T]GTGGGACTCTACGAT | 7464 |
rs781472802 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98173883 | GCACTTTGGGAGGCT[A/G]AGGCGGGCAGATCAC | 7464 |
rs781474836 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98162466 | TCCCCCAATCCTCTC[C/T]CCACCCTAACTCTTA | 7464 |
rs781506749 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141808 | AATAATCATTTCTTC[C/T]TTGCAGGATTGTTGA | 7464 |
rs781570692 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | CORO2A, TRIM14 | GRCh38.p7 | 9:98120711 | TTGGAACATTCTTCT[C/T]CCCAAATGCCCTTTG | 7464 |
rs781664363 | snp | C/T | 4.95995e-05 | 0.00497969 | missense | CORO2A | GRCh38.p7 | 9:98128182 | CACCTCGATTCATCC[C/T]GCTGAGCCACTCCTG | 7464 |
rs781700479 | snp | A/C | 5.02769e-05 | 0.00501358 | intron-variant | CORO2A | GRCh38.p7 | 9:98133013 | GCTCCTCTGAGCCTG[A/C]GCCAGCCCCTGGCCC | 7464 |
rs781703465 | snp | A/C | 8.60178e-05 | 0.00655755 | intron-variant | CORO2A | GRCh38.p7 | 9:98126962 | GGGAAATACAGCTAC[A/C]TGTGGACAGGCCCAA | 7464 |
rs781754244 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98125858 | GAGTAGCTGGGACTA[C/G]AGGCACGCACCACCA | 7464 |
rs781766444 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98176458 | GTGGACTTCCTCGCA[C/T]CTACTGAACAGAAAT | 7464 |
rs796102535 | in-del | A/TTT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98141354 | CCACTGACCCTTTTT[A/TTT]TTTTTTTTTTTGGAC | 7464 |
rs796112752 | in-del | -/AC | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158837 | ATTAAAAAGAAGAAA[-/AC]ACACACACACACACA | 7464 |
rs796121789 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158290 | GTCTCTAAAAAAAAA[-/A]TAAAAGAGAGAGAGA | 7464 |
rs796167459 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148100 | AAAAAAAAAAAAGAA[A/G]AAAAAAAAAAGAGGC | 7464 |
rs796208283 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148818 | AAAACACAAAAAAAA[-/A]TGATCAATACTCAAT | 7464 |
rs796253260 | in-del | -/AT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154363 | TATATACACAAATAC[-/AT]ATATATATATATTTT | 7464 |
rs796281156 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98144193 | GATCCTGTTTCGAAG[-/A]AAAAAAAAAAAAAAG | 7464 |
rs796294763 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98139062 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAAATGCAG | 7464 |
rs796312035 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174627 | GGTTTCCCCCAGGCT[A/G]TTCTGGTATTACTAA | 7464 |
rs796345917 | snp | C/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98179253 | GATCTGGGACCGCTA[C/G]AGCATGAGGATTCTG | 7464 |
rs796367347 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98151817 | CATGCCCGGCTAATT[A/T]TTTTTTTTTTTTTTT | 7464 |
rs796394888 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189923 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 7464 |
rs796433393 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98177608 | AGAAACTGGGATTAC[A/G]GGCATGTGCCACCAC | 7464 |
rs796435510 | multinucleotide-polymorphism | CTC/TTT | | | upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98192726 | CCAAGGTCCGCCCTT[CTC/TTT]CCCGCCCCGCGGGTC | 7464 |
rs796441340 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184073 | GTGTGTGTAGGTTAC[A/T]TGTAAACACTATACT | 7464 |
rs796445684 | in-del | -/A | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148096 | TATTAAAAAAAAAAA[-/A]GAAAAAAAAAAAAAG | 7464 |
rs796463160 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO2A | GRCh38.p7 | 9:98186887 | GCACTGAGCTCACTG[C/T]CCAGGTCCCACAGCA | 7464 |
rs796533070 | snp | C/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98134525 | CCAATGATAGTTGCT[C/T]TCCTCTTCCTATAAG | 7464 |
rs796571328 | snp | A/C | | | intron-variant | CORO2A | GRCh38.p7 | 9:98158198 | TGCCTGTAATCCCAG[A/C]ATTTTGGGAGGCCAA | 7464 |
rs796601046 | snp | A/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98189898 | CTTTATTTTTTTTTT[A/T]TTTTGAGATGGAGTC | 7464 |
rs796696078 | snp | G/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98152135 | TTTGCTGTTTTTTTT[G/T]TTTGTTTTTTCTTTA | 7464 |
rs796763532 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131331 | CCCTTAACAAATCAC[-/T]TTTTTTTTTTTTTTG | 7464 |
rs796781549 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98156050 | TGCTCTTTGTTTGAA[-/TT]TTTTTTTTTTTTTTT | 7464 |
rs796800602 | in-del | -/TA | | | intron-variant | CORO2A | GRCh38.p7 | 9:98154350 | ATATATATATATATA[-/TA]TACACAAATACATAT | 7464 |
rs796831893 | in-del | GA/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98149946 | TTCTTTTTTTTTTTT[GA/T]AGAGAGTCTCGCACT | 7464 |
rs796838945 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98126053 | TTTTTTTTTTTTTTT[-/T]AAGATGGAGTCTTGC | 7464 |
rs796856711 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148099 | TAAAAAAAAAAAAGA[A/G]AAAAAAAAAAAGAGG | 7464 |
rs796858603 | in-del | AGAA/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148096 | ATTAAAAAAAAAAAA[AGAA/G]AAAAAAAAAAGAGGC | 7464 |
rs796927471 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO2A | GRCh38.p7 | 9:98174876 | GTGGACTAATACAGA[G/T]GGCTGCACAATGGGA | 7464 |
rs796928669 | in-del | -/TT | | | intron-variant | CORO2A | GRCh38.p7 | 9:98131331 | CCCTTAACAAATCAC[-/TT]TTTTTTTTTTTTTGA | 7464 |
rs796979528 | in-del | -/T | | | intron-variant | CORO2A | GRCh38.p7 | 9:98184243 | TTTTATTTTTTTTTT[-/T]AATAGAGGCAATGTC | 7464 |
rs796979761 | in-del | -/T | | | utr-variant-3-prime | CORO2A | GRCh38.p7 | 9:98121424 | AACAAAAATGTAATT[-/T]AAAAAACAGATGGTT | 7464 |
rs797004715 | snp | A/G | | | intron-variant | CORO2A | GRCh38.p7 | 9:98164495 | TAAGGCCACCCTGCT[A/G]CCAACCTAGGCCTCT | 7464 |
rs797015948 | in-del | -/AAAG | | | intron-variant | CORO2A | GRCh38.p7 | 9:98148094 | TCTATTAAAAAAAAA[-/AAAG]AAAAAAAAAAAAAGA | 7464 |