SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs185366449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674166 | AGCCCTTGGAACAAG[A/G]AATCATTTTGACTTT | 23603 |
rs185396759 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108689056 | AAAAAAAAAATTAGC[C/T]GGGCATGGTGTTGGG | 23603 |
rs185475941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717447 | TTAAAAGCTCACGCT[C/G]AATGAAGCTGGAGAA | 23603 |
rs185477723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684279 | ACTGGTGAAAATGTA[A/G]AAGTATAAATATAAG | 23603 |
rs185489437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690916 | GGTTGTCTAAGCCCT[C/T]GTAGTAAGCAAATGA | 23603 |
rs185492297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664381 | GGTTCAGCTCAGTTC[G/T]ACTGTCCTGCAAAAA | 23603 |
rs185523427 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712376 | CTCAGGAATTCGAGA[A/C]CAGCCTGGCCAACAT | 23603 |
rs185537638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663333 | CCACTCCTAGGGATA[A/T]ACCCAAGAGGATGGA | 23603 |
rs185642080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108669079 | TGAAAGGTAAACTGT[A/G]TCAATATAATTTAAT | 23603 |
rs185795918 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702160 | TTACACAGGAACAAG[C/T]TCAAAGCCAGGTACT | 23603 |
rs185834967 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108724573 | ATATAGGTCCACAGA[A/T]GATCATCACAAGGCA | 23603 |
rs185857886 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108672073 | TGCCCAATCATTTTA[A/T]ATTCAGAGAAACTCA | 23603 |
rs185882862 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696627 | AGCTTGTGCAGTTGT[G/T]GCAAGAAAAAAAAGT | 23603 |
rs185884709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108719339 | AAATAACACACACAC[A/G]TATACACACAAATGC | 23603 |
rs185886941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672823 | ACAGTGATCAGTAAT[A/G]TCTGATGTTACTACT | 23603 |
rs185966090 | snp | A/T | 0.00199481 | 0.0315187 | synonymous-codon, intron-variant | CORO1C | GRCh38.p7 | 12:108702923 | GTTATTGCCAGACTT[A/T]CCCAGCTGACTACCA | 23603 |
rs185978639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654849 | TGGGATTATAGATAG[A/G]CACATGCCACCACCC | 23603 |
rs185999722 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646500 | TGACCAAAACCTGAA[A/G]CATGATGTTTAAAGT | 23603 |
rs186033239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696393 | ACAGGCTTGTTGTGA[C/T]ATGAAGTGTGTCGGG | 23603 |
rs186048384 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647065 | AAGGGTACTTGGGCA[C/T]GACACAATCAGAATT | 23603 |
rs186088860 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652849 | CGCAATGCTGTTATG[C/T]CAGTATGATGATAAA | 23603 |
rs186092126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679391 | CAATTTGCTCATGTC[A/G]CACATTTGAATCTAG | 23603 |
rs186121922 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108723730 | TAATCAACCTTTGCT[A/T]ATCCTAAGTGGTTTT | 23603 |
rs186124810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108725984 | TGGGACTACAGGCGC[A/G]TGCCACCACACCCGG | 23603 |
rs186129808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108701472 | TTGCAATCCAAATTT[A/C]TTTTAGCAGCACATA | 23603 |
rs186131689 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108677824 | AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT | 23603 |
rs186210280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684384 | CAATTTGGTAACAGG[C/T]AGAGGTGAGGAAGTC | 23603 |
rs186249602 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731696 | TCGCTACGCCCCCTC[C/T]GGTCGCACCGAGGGA | 23603 |
rs186361842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108707192 | ATGAAGGGATTGATT[A/G]GAACTGCAAGGGATC | 23603 |
rs186368154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659486 | CACTCAGAGAGAAGA[C/T]CATTATTACTTTTTT | 23603 |
rs186633475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712177 | GTAGAAGAGATCCGA[C/T]GTGTTATTCAATAGA | 23603 |
rs186644330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688659 | CACCTGTAATCCCAG[A/C]ACTTTGAGAGGCCGA | 23603 |
rs186647976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661645 | ATTTGCCTAATAGGG[G/T]TCTCCCAAAGCTGGC | 23603 |
rs186686706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714949 | CAATGTGAAGCAGAA[A/G]GCAGTGAGCGCATTG | 23603 |
rs186690393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108677999 | ACTCCAGCCTGGGTG[A/G]CAGAGCAAGACTCCA | 23603 |
rs186691787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693093 | TTGAGCCACCGCGCC[C/T]GGCTAAACCACAGAT | 23603 |
rs186694789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667353 | GCTTTTCTTTGTTCT[A/G]TGGCTACAGACTGGT | 23603 |
rs186872705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654054 | TTGGAGCATTTTCCC[C/T]AATACCCCAGCCCAA | 23603 |
rs186892316 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108661526 | TGAGTGGTGGGATTA[A/T]AAGTGATTTTTTTTT | 23603 |
rs186969122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719980 | ACTTGAGCCCAAGAG[C/T]TGGAAACCAGCCTGA | 23603 |
rs186978980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658369 | CATCTTTAACAGCTG[C/T]GTTTGGAAAAGGGTG | 23603 |
rs187086779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108691441 | AGATACCTTTCTTTA[C/T]CGGAGATACAGCAGC | 23603 |
rs187268371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108714209 | TCCTGGCCAACATAG[C/T]GAAACCCCATCTCTA | 23603 |
rs187308846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666408 | GGTGGTGTTCTCTAC[A/G]GTGGACTGTGGAAAG | 23603 |
rs187339189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108692273 | TGAATGGGCATCCCA[C/T]GACATGTCAGGACAC | 23603 |
rs187502026 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CORO1C | GRCh38.p7 | 12:108727262 | GATGAATGTACAATA[C/T]ATGAGGGCAGGGACA | 23603 |
rs187536158 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733319 | TGAGACTACAGGCAC[A/G]CGCCACCATGCCCAG | 23603 |
rs187539352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698762 | GAGAAACAGAGGAGC[A/G]GAAGGATAAAGAGAC | 23603 |
rs187540634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108674625 | GAAAATTCATGATTC[A/G]TGGAAGGAGTTCTAA | 23603 |
rs187545427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649754 | CTTTTTCAGTCAAGA[C/T]GGGAAACAACAAAAA | 23603 |
rs187583054 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108721612 | ATCAAGTCCCTAATA[C/T]ATTTTGCATCATAAA | 23603 |
rs187588433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720941 | TTGAAATTCAATTAC[G/T]CAATTAACATTTATT | 23603 |
rs187655186 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704949 | TAAAGTTGAAGTGAT[A/C]ATTAAATGATCAATT | 23603 |
rs187782932 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108680533 | CCCAGAGTGTAGTCA[C/T]GGTTCTGCCATCTTC | 23603 |
rs187783173 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655156 | TGATCTATTTCCTTC[A/C/T]GACACATGTACACAG | 23603 |
rs187829510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698406 | ATTTCCAAGGCAGAA[A/G]ATAACTTTTTTTTCT | 23603 |
rs187833166 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108648144 | CCCACACCGCCAGAT[C/T]CTTCTGTCGTAGCCA | 23603 |
rs188008972 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704130 | AAAATGCTTTGTCTT[C/T]ATTGAAAGATACTAT | 23603 |
rs188012652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108726424 | AGAGTGAGACTCTGT[C/T]TCAAAAAAAAAAAAA | 23603 |
rs188102706 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO1C | GRCh38.p7 | 12:108687560 | GAGGCTGAGGCGGGC[A/G]GATCACTTGAGGTCA | 23603 |
rs188190586 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657897 | AAGATGTCGGGTGGA[A/G]AAAACACTTAACACA | 23603 |
rs188329836 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108714385 | GCCTGGCAACAGAGC[A/G]AGAGTCAGTCTCAAA | 23603 |
rs188331987 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108681367 | TGCACAAATCCCACC[A/T]CCGGCAGTATAAGTG | 23603 |
rs188366137 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108711066 | CCATGTGAAGTTAAA[G/T]GTACAAAATTTACAT | 23603 |
rs188378527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695484 | AATTCTAACCATTCC[C/T]TCCGTTAAGTGAATA | 23603 |
rs188378693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718813 | TATAATAGAGTACAA[G/T]AAACTAAGAATTTAA | 23603 |
rs188387975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660973 | AACTGCCCCTCCTCC[C/T]TTTTACTGGTGAGGG | 23603 |
rs188424149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108709243 | AGCATAGAATCTGAA[A/G]CATAGTACATACTGT | 23603 |
rs188618736 | snp | C/G/T | 4.94828e-05 | 0.00497387 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657346 | GCTCATGCGGCTGAA[C/G/T]CCAGTGGTGAAGACA | 23603 |
rs188647628 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704424 | CTTCAGTGAGCCAAG[A/G]TCGCACCACTGCACT | 23603 |
rs188666240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685938 | TTCAAGGGCTTACAC[C/T]TCTAAGTATCTTCTT | 23603 |
rs188799796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108690461 | AAGCAAATAATTTTT[A/G]CATCACAGATCCTCT | 23603 |
rs188814480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108699723 | TTATAACAGTGTAGT[A/G]TACTTATCTGCCACT | 23603 |
rs188816889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663991 | TTTATGTTTAACAAT[A/G]AACAACAAAGGTTTC | 23603 |
rs188818448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722231 | AAATGACATGAATAA[A/C]GCCTGTAGTCATCCC | 23603 |
rs188885658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694139 | ATATAAAAATTAGCC[A/G]GGCATGATGGTACAC | 23603 |
rs188887301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717474 | AGAATGGATCTGCAC[A/G]TGGGAGCATCTGAAA | 23603 |
rs188974821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108723586 | AAGGCCTCAGCAGTT[A/G]TTGAGACATGGGGAC | 23603 |
rs188988367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108653049 | CAACCTGAACAATGA[C/T]GGCAATCTTGTCTGG | 23603 |
rs189016020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108701767 | TGTGGCTTTGTCCTC[A/G]GCCTGCCAAGGTAAT | 23603 |
rs189018152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724296 | CACTGGGTCAAAGAC[C/T]ACAAAGGGAAAGCCA | 23603 |
rs189031992 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108677900 | AGCAGATGCCTGTAA[A/T]CCCAATTACTCGGGA | 23603 |
rs189051153 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108694431 | ATAGTTAGCTCTTTA[C/T]ATGTACTCTGGTAAT | 23603 |
rs189055489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670561 | TATTAGAAAGCAAGG[A/C]ACCATGTTTCTGAAC | 23603 |
rs189071650 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645436 | TTTACTTCATTAATT[C/T]GATATCAGAACCTTA | 23603 |
rs189151501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676951 | ATGAGATCACAGGAG[C/G]AGACATTCCCAGCCA | 23603 |
rs189170054 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669501 | ATGGAAGGCAACTGG[G/T]GCTGAGAGCGTTTAA | 23603 |
rs189198875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716607 | TCAGACACAAATTTA[A/T]CTTGACATAATTACC | 23603 |
rs189232057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671759 | GTGAGTCAATAATTT[C/T]ATTTATTTATTTATT | 23603 |
rs189281616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700885 | CATGCTCACAACATC[A/G]TTATAATAATTTTTT | 23603 |
rs189427942 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658188 | CTTTTCGCCCTGCGC[A/T]TTTATTTATTTATTT | 23603 |
rs189443801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651783 | TTAATTCCACAGTAC[A/T]CACAAGGATAGAAAG | 23603 |
rs189449723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705408 | GAGGTCGCAGTGAGC[C/T]GAGATCACGCCACTG | 23603 |
rs189455736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730453 | CATTTGAGAGACGGA[A/G]AGCTGGGGAGCGTGC | 23603 |
rs189459894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108682479 | TAAAGAAACAATTCA[C/T]TGGAAAGTTATATTG | 23603 |
rs189519591 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646048 | GGGCAGGTTAGTTGT[A/G]CGGAGGGACATGTTT | 23603 |
rs189527886 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108681683 | AGAATTTACCATGGG[C/T]AAACCCTTGTTCAAA | 23603 |
rs189655299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691143 | ATGGCTGAGTCAGTT[C/T]CACACAAGCAAGAGG | 23603 |
rs189657386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665070 | GTCTCACTCTGAGCA[C/T]AGCTAGTGCATTTTC | 23603 |
rs189696329 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108654907 | CACAGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 23603 |
rs189702029 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108713797 | CCGAATCATATATAC[A/G]ATTCAGTTTCTCCAC | 23603 |
rs189708067 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108651464 | GTAGAAATTATATCA[C/T]AGCTGAACTTCCTAA | 23603 |
rs189808619 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108684286 | AAAATGTAAAAGTAT[A/G]AATATAAGTGCTGAC | 23603 |
rs189829111 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731172 | CCCCACAGGGACCCT[A/G]CTTCACGCTCCCCAC | 23603 |
rs189931340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108684994 | CCTTGATGGCCAACT[A/G]TAGTACTGAGCTCTG | 23603 |
rs189935805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659877 | AAACTGTAATCAAGT[A/C]GCTACATAGATTCAG | 23603 |
rs189945439 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108676382 | ACACACTATTTTTTT[A/T]AAAAGGATAACGTGA | 23603 |
rs190010388 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713597 | GGCTCGGGCCTCACA[A/G]AGCTAGGCCTGGAGA | 23603 |
rs190016219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720261 | ACAGCCATAAGAAAC[C/T]CATGCTGCCAATAGT | 23603 |
rs190047189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108713237 | TGAAAGAGATTTGTA[C/T]TCCACTGCTGATATG | 23603 |
rs190053875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108706430 | ACAGGTTCTAGCCAA[A/G]GCAATTAGGCAAGAA | 23603 |
rs190061856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663491 | TACACTGGAATATTA[C/T]TTGGCCATAAAAAAG | 23603 |
rs190067519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659030 | ATGCAGAGAGAGAGA[C/G]AGAGAAAGAGAGAGA | 23603 |
rs190258075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108666860 | AGCACCACCCTAATA[A/G]GAAATACTGCAACTA | 23603 |
rs190279133 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108714597 | AAAACTCCATCTCTA[C/T]CAAAAATACAAAAAA | 23603 |
rs190294020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692616 | CAAATGTGAACTGCT[A/G]CGATTTCATCACTGT | 23603 |
rs190297136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108689125 | GAATCACTTGAACCC[A/G]GAAGGCGGAGGTTGC | 23603 |
rs190297841 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725224 | TCAGTGACTCAACTT[G/T]GATTCAAAGTCTAAA | 23603 |
rs190312570 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647252 | TTGAGTTCTTACTGG[A/T]ATGTGGCCTATCGCT | 23603 |
rs190339734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720055 | GCCAGGCATAGTGGC[A/G]TATGCCTGTAATCCC | 23603 |
rs190344172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696705 | GCTATTATTCATCCT[C/T]TGAAGGACTAAAGAA | 23603 |
rs190348205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672911 | AAACGCTGTGTGTTT[C/T]CTCATTGCTCCACCA | 23603 |
rs190560244 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108696422 | GGGGGAGGGAGGGGA[A/C]GGGGGGGTTGTATGT | 23603 |
rs190617656 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108679455 | TCAACTAAGACAACT[A/G]CTATTGTTAACAATG | 23603 |
rs190656012 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108726241 | GCTAACACAGTGAAA[C/T]CCCATCTCTACTAAA | 23603 |
rs190788389 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108719385 | CATTTTTTGTGACCA[C/T]TTATCGTGAATACAA | 23603 |
rs190868606 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704110 | GAAGATTAATATAAA[C/T]ATGTAAAATGCTTTG | 23603 |
rs190980155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726839 | CTGAGGAGACTGTGC[A/G]CCAGTCATTACTGTT | 23603 |
rs191093541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674191 | GACTTTCAAATCTTA[C/T]TATTTAAGAAATACA | 23603 |
rs191097935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707455 | TCTTCTCAACAGATG[A/G]TACTGGGACAATACG | 23603 |
rs191109349 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648633 | TCTGTGGTTTTCTTG[A/G]GGATGCTGATCAGGT | 23603 |
rs191136849 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657984 | TTGAAAAGAGATGCA[A/G]CCAAAGAACAACCAC | 23603 |
rs191141221 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108693521 | CAATCAAGGAAAATA[C/T]CAATTTTGCCAAATT | 23603 |
rs191142548 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108715164 | CCTTGAGCCCAGGAG[C/T]CTGAGGCTGCACTGA | 23603 |
rs191162619 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108705233 | CCTGTAATCCCCACA[C/T]TTTGGGAGGCCGAGG | 23603 |
rs191179245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681789 | GAAAAGAAAGTAAAG[G/T]AGAAAGGTATAGCAA | 23603 |
rs191186857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685435 | AGCTAGGAACTGTCT[A/G]AAGACCTTGATAACT | 23603 |
rs191192857 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108660588 | GGCAAACAGGTAACT[G/T]CAGCCCCGGCAGCTG | 23603 |
rs191208091 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732595 | AAATACCGAGATTTG[A/G]GGAAACAGAGCCTGG | 23603 |
rs191217806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708403 | GACATACTAATTTAT[A/G]TGAAAGTCCAGAATA | 23603 |
rs191334029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702615 | GAACATGGTTCAACA[C/T]CGACAACTCAGCTGA | 23603 |
rs191334197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697910 | TTATTCAAATATTCA[C/T]GACTATACCAAAATT | 23603 |
rs191348479 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731708 | CTCTGGTCGCACCGA[A/G]GGATGCAGGCGGTGC | 23603 |
rs191354515 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654504 | TATTCTTCTATCCCA[A/T]TTAAGCGAGCCATTT | 23603 |
rs191451740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686010 | ACCAAATCAGCATAC[A/G]TTATTAAAAATACAA | 23603 |
rs191582717 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108661528 | AGTGGTGGGATTAAA[A/C]GTGATTTTTTTTTCC | 23603 |
rs191589715 | snp | C/T | 0.000148707 | 0.00862158 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678334 | GTGGGCACCAGTCTA[C/T]GTCCAGCACTGGTCC | 23603 |
rs191606787 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108711193 | CATAGCGAGACCCCA[C/T]ATCTACAAAAAATAA | 23603 |
rs191628437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687834 | AGAAAAAAGAAGAAA[C/T]GATATTGCTTAGCTG | 23603 |
rs191664676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661067 | AAGGTATAACTTACA[C/T]ACAATACAATGCACC | 23603 |
rs191665085 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108666126 | GAACAAGACTTAGGT[C/G]AAAGTAGAGCAGAAT | 23603 |
rs191705627 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108710037 | GCAACAGAGTTTTTA[A/G]CCTCTACAAAACATG | 23603 |
rs191824146 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108717799 | GAAAAATACTTTAAA[A/T]TTTATTTTTTAAAAC | 23603 |
rs191885791 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108714240 | CTAAAAATACAAAAA[C/T]TAGCAGGGCGTGGTG | 23603 |
rs192016347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674638 | TCGTGGAAGGAGTTC[C/T]AAATATCAACATTTG | 23603 |
rs192019337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108650096 | TTTATAAAATCATCA[C/T]CCTCTTTAAAAGGAA | 23603 |
rs192050405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108699303 | CTCAGTTTCTCATGG[C/T]CTGTAAAAGCAAAGA | 23603 |
rs192054742 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108721633 | GCATCATAAAATGTT[G/T]GAATGAAAAGAGTTC | 23603 |
rs192069238 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646603 | ATCTGAAGCACAGGA[A/T]AACCGAGAAGCAAAA | 23603 |
rs192207680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108691766 | CCGGCTGCTGTGGAC[A/C]TATCAGTGAACTGCA | 23603 |
rs192211860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108729849 | AACAGACGGTACAAA[A/G]CAACTGCTTATACTT | 23603 |
rs192430514 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108672662 | TTTTTGTTTTGTTTT[G/T]TTTTTTAAACAAATT | 23603 |
rs192440808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108680721 | TCAATAAACATTACC[C/T]GAAATTTAACAAATG | 23603 |
rs192456509 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108655723 | GTGGTGTGATCTCGG[C/T]TAGCTACAACCTCCA | 23603 |
rs192473460 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704132 | AATGCTTTGTCTTCA[C/T]TGAAAGATACTATAC | 23603 |
rs192505801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712209 | AAAGGCAGGTAAGAC[A/G]GCAGATGAGGAGACA | 23603 |
rs192514826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688763 | AATACAGGCCGGGCA[C/T]GGTGGCTCACACTTG | 23603 |
rs192599640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108668066 | CCATAAAAAGGGTTA[C/T]ACCCCCAAAAGACCC | 23603 |
rs192669848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722233 | ATGACATGAATAAAG[C/T]CTGTAGTCATCCCAA | 23603 |
rs192710037 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108649412 | GATTGTATCTACAAC[A/G]CGGGTACAAGGTCTT | 23603 |
rs192724190 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704427 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA | 23603 |
rs192795242 | snp | A/G | 6.59663e-05 | 0.00574272 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657370 | GAAGACATTGCCATC[A/G]GCCAGGAAGATGGCT | 23603 |
rs192880239 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651580 | GTTCTTCCACTCATA[A/G]GGTAGGAAAACCACC | 23603 |
rs192895231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700388 | CTATAGATTTTGATC[C/T]GCAGTATTCATGATT | 23603 |
rs192913091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727997 | GAAAAGATGCTCAAC[A/G]TCATTAGCCATTAGG | 23603 |
rs193002120 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108681460 | TCCCAGAAGCAACAA[C/T]AGAGAAAGGACAGAT | 23603 |
rs193073074 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108669612 | TATACTATCTACTAT[C/T]TGTAGCTCATGAGCT | 23603 |
rs193084989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717425 | GTGACATAATTAGAT[C/T]TGCATTTTAAAAGCT | 23603 |
rs193102228 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108662469 | GCCTCAGACTCCCAA[A/G]TATCGGCTGTTTTTA | 23603 |
rs193149067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698430 | TTTTTCTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 23603 |
rs193237899 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694237 | CAGTGAGTCAAGATC[A/G]CACCACTGCACTCTA | 23603 |
rs193240173 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644944 | GACTGGCTTGGAGAC[C/G]TCACTTGTACTTGAA | 23603 |
rs193257289 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721424 | TGTCTCCTGAATTCC[C/T]ACAGAGCTCACAGTC | 23603 |
rs193301018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674364 | CCATCCTGGCTAACA[C/T]GGTGAAACTCCATCT | 23603 |
rs199536498 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721929 | GAAAAGAAAAAAAAA[-/A]GATCAGAAAGTATTT | 23603 |
rs199555485 | in-del | -/A | 0.00353101 | 0.0418693 | intron-variant | CORO1C | GRCh38.p7 | 12:108654453 | TATGTGTATGTATAC[-/A]TTTTTTTAAAAATAA | 23603 |
rs199580254 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647952 | AGCTCCTGCCATCTG[G/T]GAGGCTCCTTCTTGG | 23603 |
rs199604203 | in-del | -/AAAG | 0.0142736 | 0.0832652 | intron-variant | CORO1C | GRCh38.p7 | 12:108713004 | CCAGCAGTGACACTC[-/AAAG]AAAGAATTTACCTAA | 23603 |
rs199641177 | in-del | -/AATAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671031 | AGTCTAAAAAAAAAG[-/AATAA]AAAAAAAAGGTTTAG | 23603 |
rs199668001 | snp | C/T | 0.000999623 | 0.0223341 | intron-variant | CORO1C | GRCh38.p7 | 12:108678430 | ACCTATTATGTAATA[C/T]CAACACCACAGACGT | 23603 |
rs199738350 | snp | C/T | 0.00125728 | 0.0250411 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658723 | CTACTGAGTTTTCAT[C/T]CTAGGAATACTCACA | 23603 |
rs199780637 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652846 | TAACGCAATGCTGTT[A/C]TGCCAGTATGATGAT | 23603 |
rs199816321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716707 | AATGATTTCTAGGGT[C/T]CTATCAGAGTCTACA | 23603 |
rs199820373 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679187 | AAAAAAAAAAAAAAA[C/T]AAAAGCTTTAGCTAT | 23603 |
rs199841328 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674553 | ACTCCGTCTCAATTT[A/T]AAAAAAAAAAAAAAA | 23603 |
rs199881668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662189 | GAAAGATGATCCACA[C/T]GAAAGCTATTGCCTT | 23603 |
rs199929735 | in-del | -/A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706196 | GAATCAAAAAAAAAC[-/A/C]AAAAAAAACAAAAAA | 23603 |
rs200001763 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687925 | CCTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 23603 |
rs200154631 | in-del | -/TGTA | 0.0138799 | 0.0821421 | intron-variant | CORO1C | GRCh38.p7 | 12:108678099 | CTTGAAAGGATTATC[-/TGTA]TGTAATTAAACTTAA | 23603 |
rs200237779 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709131 | GATTATATATATATA[-/TA]CTATAAACCGCTGAA | 23603 |
rs200256524 | in-del | -/AAAG | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659217 | CAACCAAACAAAAAC[-/AAAG]AACCACACCAAAACA | 23603 |
rs200269891 | snp | A/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648977 | CCTTCCTGGGAACAG[A/T]CATAATAATAGGTTC | 23603 |
rs200301426 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729392 | TATGTTTCATCGGTA[G/T]GTATCTATTAAAATT | 23603 |
rs200317812 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | CORO1C | GRCh38.p7 | 12:108701015 | CTTCAATTACATCAG[-/A]GTCTAATGGTTTCAC | 23603 |
rs200378163 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | CORO1C | GRCh38.p7 | 12:108712265 | GACAATGCCAACAGT[-/A]AAAAAATTCCTTTTA | 23603 |
rs200384833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108657297 | GGAAAGCCTGGGGAG[A/G]GCGTACCGGATTCCA | 23603 |
rs200401456 | snp | C/G | 0.000148492 | 0.00861532 | intron-variant | CORO1C | GRCh38.p7 | 12:108648885 | CCCGTGGGTAAGGAA[C/G]AAGAAAGGCCTGGGA | 23603 |
rs200440595 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662318 | GACCGTGTTAGGCGG[-/T]TTTTTTTTTGTTTGT | 23603 |
rs200613507 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662479 | CCCAAGTATCGGCTG[A/C]TTTTAAAATGTAATA | 23603 |
rs200616346 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674038 | GATCAGGAAAAAAAA[-/A]GATTCCTTACAAAAT | 23603 |
rs200626934 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108685614 | TATGCCATGGGTTGT[-/A]AAAAAAAAGGCACAC | 23603 |
rs200628009 | snp | A/C/G | 1.64743e-05 | 0.00287 | missense, synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701127 | CAAATTACCTACCTT[A/C/G]TGCAGAGGGAGGACA | 23603 |
rs200632468 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683454 | AAAAAAGAAGTCAGT[A/G]GAAAAAAAATAAATA | 23603 |
rs200644659 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | CORO1C | GRCh38.p7 | 12:108713083 | ATGAGACATTCCAAG[-/A]AAAAAAAAACATGCC | 23603 |
rs200731013 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652852 | AATGCTGTTATGCCA[A/G]TATGATGATAAAAAG | 23603 |
rs200777717 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699440 | CCATTTCTTTGAAGG[-/A]AAAAAAAAAGTCTTA | 23603 |
rs200803526 | snp | A/C/G | 0.000132106 | 0.00812631 | synonymous-codon, missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662138 | GGAAAGGGTGAGTCC[A/C/G]TTTTCTGGGATCTGC | 23603 |
rs200862690 | in-del | -/TAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655096 | ATAAAAATCATTCCA[-/TAT]TCAAAATCCTACAGC | 23603 |
rs200939076 | snp | A/G | 0.00196992 | 0.0313222 | intron-variant | CORO1C | GRCh38.p7 | 12:108678444 | ATCAACACCACAGAC[A/G]TTATACATTTTCTCA | 23603 |
rs200942346 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706205 | AAAAAACAAAAAAAA[A/C]AAAAAAAAAGCATTT | 23603 |
rs200947296 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720538 | GAATTTTTTTTTTTT[A/T]TTTGAGATGGAGTCT | 23603 |
rs201027647 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683455 | AAAAAGAAGTCAGTG[A/G]AAAAAAAATAAATAA | 23603 |
rs201118257 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648646 | TGGGGATGCTGATCA[A/G]GTCGCACTTCTTGTT | 23603 |
rs201128993 | in-del | -/T | 0.0252325 | 0.109451 | intron-variant | CORO1C | GRCh38.p7 | 12:108683905 | TCATCATATAAGGAA[-/T]TGTAACACCTTGATA | 23603 |
rs201152683 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732816 | AAAATGGGGATAACA[C/T]CCCCTCCCTCACAGG | 23603 |
rs201158194 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647041 | TTGGTCCCTATTCAT[A/T]AAAAAAAAAAGGGTA | 23603 |
rs201163122 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645250 | AAAAAAAAAAAAAAA[C/T]ACAAAACAGGAAAAT | 23603 |
rs201235612 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | CORO1C | GRCh38.p7 | 12:108713903 | GTGTAACACTTTAAA[-/T]GTGAAACTGCACTTT | 23603 |
rs201246912 | in-del | -/T | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733501 | GAACAATAAAAGTTG[-/T]TTTTTTTAAAATCCA | 23603 |
rs201309211 | in-del | -/T | 0.172997 | 0.237846 | intron-variant | CORO1C | GRCh38.p7 | 12:108672658 | GGTGTTTTTGTTTTG[-/T]TTTTTTTTTTAAACA | 23603 |
rs201309864 | snp | A/C | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662068 | CCGTTGGATGCCAAG[A/C]CACGATGCCGACTCT | 23603 |
rs201309986 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678737 | AAAAAAAAAAAAAAA[-/C]CCCTAAACCTTGGTA | 23603 |
rs201350047 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108672642 | CACAGATATTGTGGT[-/G]GGTGTTTTTGTTTTG | 23603 |
rs201372015 | snp | A/G | 0.127944 | 0.218179 | intron-variant | CORO1C | GRCh38.p7 | 12:108674441 | TAGTCCCAGCTACTC[A/G]GAGGGCTGAGGCAGG | 23603 |
rs201435259 | snp | C/T | 1.66324e-05 | 0.00288374 | intron-variant | CORO1C | GRCh38.p7 | 12:108652447 | AGACAAGTCTGTGTC[C/T]GATTGTTAACTGAAA | 23603 |
rs201449273 | in-del | -/GATGGC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666562 | TCTGCTACTCTGGGT[-/GATGGC]CTGCTCGGTTTGGAC | 23603 |
rs201458763 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675194 | GTATATATATATATA[-/TA]CATAATGCTACTGCA | 23603 |
rs201464647 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660474 | AAAAAAAAAAAAAAA[C/T]AAGTAGGAAACTGGA | 23603 |
rs201474432 | snp | C/T | 0.463234 | 0.130503 | intron-variant | CORO1C | GRCh38.p7 | 12:108652055 | AGATTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 23603 |
rs201562140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654260 | TCTGAAGGATAAATG[C/T]TTCCACTTACAGGAT | 23603 |
rs201562296 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108718765 | CTTCTAAAGCGAAGG[-/A]AAAAACAAAACAAAA | 23603 |
rs201573103 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | CORO1C | GRCh38.p7 | 12:108652042 | AAAAAAAAAAGTGAG[-/A]TTTTTTTCTTTTCTT | 23603 |
rs201586994 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705859 | TTATATCAATAGAAG[-/A]AAAAAAAAATCACAC | 23603 |
rs201627462 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690295 | GAGGTAAAAGGAGGT[A/G]CTCTGGAATAAACCC | 23603 |
rs201679556 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708920 | ACCACACCAGGCTAA[-/T]TTTTTTTTTGGTAGA | 23603 |
rs201693239 | in-del | -/AAG | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108669785 | GGAAAATAAGGTATT[-/AAG]AAGCAGGTAGGCTAG | 23603 |
rs201701310 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652853 | ATGCTGTTATGCCAG[G/T]ATGATGATAAAAAGT | 23603 |
rs201726466 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683456 | AAAAGAAGTCAGTGG[A/T]AAAAAAATAAATAAC | 23603 |
rs201740792 | in-del | -/ATTT | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108725800 | AAAGGTGCTAAGTGA[-/ATTT]ATTTATTTATTTATT | 23603 |
rs201743627 | in-del | -/CAAT | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108683750 | CCCATCACCACCTCC[-/CAAT]CAATCAATCAATCAA | 23603 |
rs201750286 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720539 | AATTTTTTTTTTTTA[A/T]TTGAGATGGAGTCTC | 23603 |
rs201868362 | in-del | -/ATA | 0.0205511 | 0.0992634 | intron-variant | CORO1C | GRCh38.p7 | 12:108700888 | GCTCACAACATCGTT[-/ATA]ATAATTTTTTCATCC | 23603 |
rs201870519 | in-del | -/G | 0.0236746 | 0.106192 | intron-variant | CORO1C | GRCh38.p7 | 12:108662324 | TTAGGCGGTTTTTTT[-/G]TTTGTTTGTTTTTTT | 23603 |
rs201885082 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706196 | TGAATCAAAAAAAAA[-/C]AAAAAAAACAAAAAA | 23603 |
rs201885146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678250 | CACTGGCCTGTGTGC[A/G]CACAACACCCTGGGA | 23603 |
rs201981270 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672645 | CAGATATTGTGGTGG[G/T]GTTTTTGTTTTGTTT | 23603 |
rs201986662 | snp | C/T | 0.000626246 | 0.0176842 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647412 | GGACCTTCAGGCTGC[C/T]ATCTTTGCCATCTGC | 23603 |
rs201996929 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709582 | TTCAGTTTTAACCTT[-/C]TAAATTAAGATGGCA | 23603 |
rs202026923 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655097 | ATAAAAATCATTCCA[A/G]CAAAATCCTACAGCC | 23603 |
rs202034576 | in-del | -/ATT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700894 | AACATCGTTATAATA[-/ATT]TTTTCATCCATAGAG | 23603 |
rs202108634 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683453 | AAAAAAAGAAGTCAG[A/T]GGAAAAAAAATAAAT | 23603 |
rs202147131 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108657482 | GACAAGGTGAGTGGA[A/G/T]AAACTCGGGCACAGA | 23603 |
rs202194858 | snp | A/C | 0.000131789 | 0.00811648 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701226 | ACTATCCCAGGTCAC[A/C]CGAGAAACCCGGATG | 23603 |
rs202201759 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657075 | AAAAAATTAAAAAAA[-/T]AAAAAATATATAGTC | 23603 |
rs202228272 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652056 | TTTTTTTTTTTTTTT[-/T]GAGATTTTTTTCTAA | 23603 |
rs202229272 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652408 | CAAAATAGCGAATAC[C/T]GCTGTCACCCTGTAA | 23603 |
rs202229601 | in-del | -/AAAAC | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108715239 | ACTGTGTCTCTTAAA[-/AAAAC]AAAACAAAACAAAAC | 23603 |
rs267603290 | snp | A/G | | | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662146 | TGAGTCCATTTTCTG[A/G]GATCTGCCATACCTG | 23603 |
rs367543909 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108688503 | TGTCCTACATATTAC[A/G]AAAGATCATTCAGAA | 23603 |
rs367547958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657890 | CCCTTAGAAGATGTC[A/G]GGTGGAGAAAACACT | 23603 |
rs367563419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108697955 | AAGAAGGCAGTCAGC[C/T]CCATAGAGAAATGTA | 23603 |
rs367576747 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712044 | CGATTACTCAAGCGT[C/T]CAGTGGGCAGAGAAT | 23603 |
rs367604350 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694800 | TACGTAGATTTTTTT[C/T]TTAAAGGCTAGGTGG | 23603 |
rs367931767 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703090 | AGGAAAGCACATCTA[C/T]ACAAAAGCCAACGTA | 23603 |
rs367933341 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646225 | AGGAATGGCTGGGGG[A/G]GCCCTGAGAGAGGTC | 23603 |
rs367940362 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652073 | TTTTTTTTTTTTTTG[-/A]GATTTTTTTCTAATG | 23603 |
rs368014175 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676812 | TCAGGTCTAAACGAT[A/G]TTCCTTTCTCTTAAC | 23603 |
rs368065251 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669767 | CCTTCAGAAGAGCAA[C/G]GTGGAAAATAAGGTA | 23603 |
rs368069278 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698608 | GACGAGGTTTCACCA[C/T]GTTGTCCAGGCTGGT | 23603 |
rs368084474 | snp | C/T | 9.88386e-05 | 0.00702919 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648775 | CTGCATTCTTGCCTT[C/T]GAACCACTCTTCTGC | 23603 |
rs368101591 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688764 | ATACAGGCCGGGCAC[A/G]GTGGCTCACACTTGT | 23603 |
rs368106069 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710852 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCTAAAAT | 23603 |
rs368130445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108664650 | CTCTCCCTCCCTCTG[C/T]GGAAGAGACCTTGAC | 23603 |
rs368147183 | in-del | -/A/AA/AAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706186 | GTGAGACTCTGAATC[-/A/AA/AAA]AAAAAAAAACAAAAA | 23603 |
rs368216647 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653787 | CAGGAACAAGAACCC[C/T]CTGGAGAGTCTCTGA | 23603 |
rs368225831 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650312 | GCCTCTGGAATAACT[C/G]GGACCACAGGTACGT | 23603 |
rs368228886 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693753 | CCACCTACTTCTTTG[C/T]CCTCCTAGGGACAGA | 23603 |
rs368364731 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709583 | TCAGTTTTAACCTTT[-/C]AAATTAAGATGGCAT | 23603 |
rs368475426 | snp | A/G | 0.000115305 | 0.00759205 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648615 | CTCACCACACTGGCC[A/G]TGTCTGTGGTTTTCT | 23603 |
rs368484021 | snp | C/T | 1.65119e-05 | 0.00287327 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662071 | TTGGATGCCAAGCCA[C/T]GATGCCGACTCTCTT | 23603 |
rs368530181 | in-del | -/AGAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713010 | GTGACACTCAAAGAA[-/AGAA]TTTACCTAACGAATT | 23603 |
rs368581516 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684775 | TTGTGAGTACATGTG[C/T]GTCCTATTATTTTGA | 23603 |
rs368594296 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108656478 | CCGGGAGGTGGGGGG[C/T]GCCTCTGCCCTGCCG | 23603 |
rs368607467 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710075 | CAAACCTTACTTGTC[C/T]TTTTAAGATGTAATT | 23603 |
rs368634686 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671149 | GCCAGCCTGGACAAC[A/G]TTGTGAGAAACCTCG | 23603 |
rs368661025 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108668550 | GAAAATTTATAATGG[A/T]AGCAAAAATGGATTA | 23603 |
rs368715896 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651248 | TTTAAAAGTCCACAT[A/G]AACACAGTGTTACAC | 23603 |
rs368755225 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CORO1C | GRCh38.p7 | 12:108648572 | GATAAAGCCTGAACC[A/G]GCCAAGCACCCCTGC | 23603 |
rs368805759 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699362 | AAGTTGAAAGGAAAT[A/G]TCTGAATTCAGAGGA | 23603 |
rs368824202 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699785 | ATCTAAATAAAAAAT[A/T]AATTTTCAACTTAAT | 23603 |
rs368824544 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682050 | GTATAATTTCTGGGG[C/G]TGGGTGGGGGTGGAG | 23603 |
rs368845779 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728185 | ACCATACAACCCATC[A/G]ATTACATTCCTAGGT | 23603 |
rs368846940 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679137 | AAAAAAAAGAAACAA[A/G]AAAAAAGAAAAAAAA | 23603 |
rs368874964 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662529 | ACCAACAAGGACTAC[A/G]AAACATTTCCTCTCA | 23603 |
rs368890006 | snp | C/T | 4.9579e-05 | 0.00497866 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657413 | GCTCCTTCATGTGCT[C/T]TCTCCTTCTCCTGGA | 23603 |
rs368923856 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108700080 | ACAGAAATTCACTTT[A/G]TTGTAACCACTCTCA | 23603 |
rs368925972 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108705398 | CTGGGAGGCAGAGGT[A/C/T]GCAGTGAGCCGAGAT | 23603 |
rs368926684 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674440 | TAGTCCCAGCTACTC[-/A]GGAGGGCTGAGGCAG | 23603 |
rs368990543 | in-del | -/AAG | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108684834 | AAATATAATAAAGTT[-/AAG]AAATACACCAATGCA | 23603 |
rs369108822 | in-del | -/GTTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722142 | TCAAAGAGACAATCT[-/GTTT]ATCAGTAAGGAACCT | 23603 |
rs369115518 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712323 | CACACCTGTAAATCC[C/T]AGCACTTTAGGCAAC | 23603 |
rs369215314 | in-del | -/TTAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665565 | GTGTGATACAGACAG[-/TTAG]AGAGTGAGCACCAGA | 23603 |
rs369220252 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694676 | AAGGTACCATGGAAT[A/G]CAGGATAACAAAATC | 23603 |
rs369260722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658491 | ACTCTAGTGAACTGA[C/T]ACAAACTATTTCTTT | 23603 |
rs369335205 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700171 | GGATCCACTTCCCCC[A/G]CTGTTTTCAGCAGAG | 23603 |
rs369375196 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687539 | CCTGTAATCTCAGCA[C/T]TTTGGGAGGCTGAGG | 23603 |
rs369416057 | snp | C/T | 1.66721e-05 | 0.00288717 | intron-variant | CORO1C | GRCh38.p7 | 12:108654436 | GATAATAATAATACA[C/T]ATATGTGTATGTATA | 23603 |
rs369494520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108708136 | CCTAGGTATACACTC[A/G]TAAGAACTGAAAACA | 23603 |
rs369528565 | snp | A/G | 8.25921e-05 | 0.00642567 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678314 | GGCAATGACCTGATC[A/G]TTATGTGGGCACCAG | 23603 |
rs369569296 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108706470 | AGAGACATTCAGATT[A/G]GAAAGAAAGAAGTAA | 23603 |
rs369599544 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678656 | AAGAGAATATGAAAG[G/T]CTTTTTGCCAAAATA | 23603 |
rs369629722 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108706789 | GGGTTTCACTATGTT[-/G]GTCAGACTGGTCTCG | 23603 |
rs369635002 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108666407 | GGGTGGTGTTCTCTA[A/C/T]GGTGGACTGTGGAAA | 23603 |
rs369644624 | in-del | -/GAA | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108720497 | TACAATAAAAATTAC[-/GAA]GTTAGTTTATAATAA | 23603 |
rs369653446 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108712042 | GTCGATTACTCAAGC[A/G]TTCAGTGGGCAGAGA | 23603 |
rs369829389 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683434 | AAAAAAAAAAAAAAA[A/G]AGGAAAAAAAGAAGT | 23603 |
rs369838008 | in-del | -/TTTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725822 | TTATTTATTTATTTA[-/TTTT]TTTGAGACGGATTCT | 23603 |
rs369882445 | snp | G/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659135 | CAAAGGAAAAAGTTT[G/T]TATAAAAGAAATAAA | 23603 |
rs369898846 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108714812 | AGAGGTATCATACTT[C/T]TTAAAGTTTTCAAAG | 23603 |
rs369914755 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689072 | GGGCATGGTGTTGGG[C/G]ACCTGTAATCCCAGC | 23603 |
rs369954232 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108694032 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCACT | 23603 |
rs369999978 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654372 | CACCCCATTGCTAGT[A/G]TCCATCTCATGAAGA | 23603 |
rs370047520 | snp | A/G | 0.000181224 | 0.0095173 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648798 | TCTTCTGCCTCCAGC[A/G]CGGCCTCTGGCCCCG | 23603 |
rs370113847 | snp | C/T | 9.91686e-05 | 0.00704092 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662054 | AAGCACATTGCGGGC[C/T]GTTGGATGCCAAGCC | 23603 |
rs370171338 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723272 | CATTTGAGTTTTTAT[A/G]TTAATAAATCAGTCA | 23603 |
rs370172867 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665190 | TAATGGGGACTTAAC[A/C]TTTTCCTTTCTCTAG | 23603 |
rs370181031 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703240 | TAGAAGAAAAAAGGA[C/T]TGCACCATGTCAGAG | 23603 |
rs370207787 | snp | C/T | 0.000543036 | 0.0164688 | intron-variant | CORO1C | GRCh38.p7 | 12:108702768 | CTAAATGCAGAGAGA[C/T]GAATTTATTTTTGCC | 23603 |
rs370240732 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108708502 | AGTCTTGCTCTGTTG[C/T]CCAGGCTGGAGTGCA | 23603 |
rs370249181 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714207 | CATCCTGGCCAACAT[A/G]GTGAAACCCCATCTC | 23603 |
rs370271921 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708462 | CATGGTTGCTTAGAG[-/T]TTTTTTTTTTTTTTT | 23603 |
rs370302682 | in-del | -/ATTGTGATGAGATGTACC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700110 | AGAATCACATGATCC[-/ATTGTGATGAGATGTACC]CTGAATATAAGGGGC | 23603 |
rs370311126 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652055 | AGATTTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 23603 |
rs370319538 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721555 | ACATTAAGCTTGCCA[C/T]AAGACTTTGTGAATA | 23603 |
rs370367624 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108679593 | CTTAATCTATTTTTT[C/G]TTGTTTTTGCTCTTA | 23603 |
rs370397321 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726858 | GTCATTACTGTTCAT[A/C/T]GGGGGAAAGAACCTG | 23603 |
rs370407476 | in-del | CC/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709583 | TTCAGTTTTAACCTT[CC/T]AAATTAAGATGGCAT | 23603 |
rs370424163 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680486 | CAGTTCATTTACAGG[C/T]AGCGAAGTATAAATG | 23603 |
rs370508323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696583 | GATTACACAGAGGGC[C/T]GAAAACCTGTGTGCT | 23603 |
rs370557330 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660502 | GGAGAAAAAAACTAC[A/G]CAACAGTAACAAAAG | 23603 |
rs370601334 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647152 | AGTTCAACAAGTCAC[A/T]TAACACTTAAAACAT | 23603 |
rs370617530 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703778 | AGGCCTGACTATGGG[A/C]CTGGATGACACCCAG | 23603 |
rs370648888 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652401 | GTGATCTCAAAATAG[C/T]GAATACTGCTGTCAC | 23603 |
rs370657775 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703625 | AAGGAGAAACTGTGT[C/G]TCTCCAAAGACAGGG | 23603 |
rs370663600 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656341 | GGAGGGAGGTGGGGG[C/G]TCAGCCCCCACCCGG | 23603 |
rs370727207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687307 | AAATCTTAAGAAATC[C/T]GGCGAAACCCTGTCC | 23603 |
rs370779615 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717888 | TCGCAAAAGTGTCTG[A/G]AGCTTGAAGAAAAAC | 23603 |
rs370800906 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108729600 | TTCTCAGTTTTATTT[A/C]ACTTTTTTCCCTACT | 23603 |
rs370865522 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704841 | TGAGAAGCACAGCTG[C/T]ACTATTTACTTCCTG | 23603 |
rs370912136 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674444 | TCCCAGCTACTCGGA[-/G]GGCTGAGGCAGGAGA | 23603 |
rs371061578 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657417 | CTTCATGTGCTTTCT[C/T]CTTCTCCTGGAGAGC | 23603 |
rs371085354 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673776 | GAGATATACCTAATG[C/T]TAAATGATGAGTTAA | 23603 |
rs371181123 | snp | A/C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720586 | TGGAGTGCAGTGGTG[A/C/T]GATCTCAGTTCACTG | 23603 |
rs371193223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108692189 | AGTCCTGTCCCCCAG[C/T]TTTTCACGGCCCATA | 23603 |
rs371212280 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701917 | ACCCTTGACTTCAAA[A/G]GCCTTCTAATCTCCT | 23603 |
rs371256282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671034 | CTAAAAAAAAAGAAT[A/T]AAAAAAAAAGGTTTA | 23603 |
rs371261218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108652012 | CCTGGGCAACAGAGC[C/T]AGACTCCGTCTCAAA | 23603 |
rs371355064 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655921 | CCCGGCCGCCATCCC[A/G]TCTAGGAAGTGAGGA | 23603 |
rs371360395 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696529 | CGTCACGAGTGTGGC[A/T]ACTCCACAAAGGAAA | 23603 |
rs371399284 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709885 | GTTCTTAAAACTGCA[C/T]AGGCTTTCCCTTGCT | 23603 |
rs371428953 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687100 | GAGTTCCTGGAGACT[C/G]ATACTTCAACTAAAC | 23603 |
rs371483646 | snp | C/G | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108649014 | TCTCTCATGAAGTTT[C/G]AAGAATCTTCAGAGG | 23603 |
rs371530054 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723938 | AAACCACTGCTTACT[A/T]GTGCTCAGATTATAA | 23603 |
rs371589750 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731674 | TTCCCACCCCACGTT[C/T]CACGCCTCGCTACGC | 23603 |
rs371616071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108726446 | AAAAAAAAAATGAAC[A/G]TAAGAACACAAAATA | 23603 |
rs371698036 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709207 | TCCAAACTGTTTTTT[-/TA]AAAAAACTATAAAGT | 23603 |
rs371733878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108729128 | CTAAGAATTGATATT[C/T]ATCCTTTTGAACATT | 23603 |
rs371757259 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108682353 | ATAATGGCACCAAAA[A/G]GCAAATAAAGGAGGG | 23603 |
rs371837215 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710209 | GAACACAGGCTCAAC[C/T]ATGAGATGCTCTCTC | 23603 |
rs371883650 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683256 | AACCCCGTCTCTGCT[A/G]AAAATACAAAAACTT | 23603 |
rs371902389 | in-del | -/AC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714454 | CATAAAACACTAGAA[-/AC]ACACACACACACCCC | 23603 |
rs371908617 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700166 | AGCGGGGATCCACTT[C/T]CCCCGCTGTTTTCAG | 23603 |
rs371922730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108664725 | CCATTACTGCATGTT[A/G]GCTTTCATCCTGACA | 23603 |
rs371929260 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653800 | CCTCTGGAGAGTCTC[C/T]GAGGCCCTCAAAAGT | 23603 |
rs371939070 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693347 | AAGGGGACTATCCAC[A/G/T]TACGATCTGCTGACA | 23603 |
rs371940032 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648709 | TGACCACCTTGAGAT[C/T]CCTGTTTTTGCCTGG | 23603 |
rs371951939 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650596 | CGAGAGTGTGACAAC[A/C]TCACCAAGCCTTAAG | 23603 |
rs371952685 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699124 | TAAACATGACAATTT[C/G]TAAAGCAACTTATTC | 23603 |
rs371955135 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669693 | AAAAAAAAAAAAAGG[C/G]GGGGGGTGGCGGGGG | 23603 |
rs371957436 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677508 | CTTGGAAACAAGCAA[C/T]TGCAAAAACTCTTTT | 23603 |
rs371978869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669453 | TTCCTTTTGACTCTC[A/G]ATAGGCATATTATTA | 23603 |
rs372123673 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676064 | TAAGACTTAAAAGAC[A/T]ACATATCAAGTTTTT | 23603 |
rs372145217 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645285 | CACAATGCTTTGGGC[A/G]CCTACTCTGAGCTTG | 23603 |
rs372198794 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721420 | CGCCTGTCTCCTGAA[C/T]TCCCACAGAGCTCAC | 23603 |
rs372286353 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715860 | TCCTTGAGGCCGGGC[G/T]GGGTGGCTCACACCT | 23603 |
rs372309959 | snp | C/T | 3.30666e-05 | 0.00406598 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654392 | TCTCATGAAGAGCAA[C/T]TGGTTCCTGCATATT | 23603 |
rs372314024 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727608 | TTTTTCATCTATAGC[A/T]TACCTTAAAATATAT | 23603 |
rs372321099 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711632 | TTGCAGTGAACCGAG[A/G]TCGCGTCACTGCACT | 23603 |
rs372334774 | in-del | CT/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702047 | ACGGGTAAGAGCCAG[CT/G]TCTGGGAAAAGCAGA | 23603 |
rs372370396 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710634 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 23603 |
rs372388219 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674655 | AATATCAACATTTGA[A/G]GAGTTCAAGACTTTG | 23603 |
rs372425688 | snp | C/T | 3.29636e-05 | 0.00405964 | intron-variant | CORO1C | GRCh38.p7 | 12:108648854 | GAAAAGGTCAGACTA[C/T]AAGAGACATTTGGCA | 23603 |
rs372442209 | in-del | -/GAGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652072 | TTTTTTTTTTTTTTT[-/GAGA]TTTTTTTCTAATGAA | 23603 |
rs372479176 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679144 | AGAAACAAGAAAAAA[A/G]AAAAAAAAAAAGAAA | 23603 |
rs372482431 | snp | A/G | 3.40849e-05 | 0.00412811 | intron-variant | CORO1C | GRCh38.p7 | 12:108678229 | TTGAAAGCAGTAGGT[A/G]AGTCTCACTGGCCTG | 23603 |
rs372553036 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679187 | AAAAAAAAAAAAAAA[-/G]AAAAGCTTTAGCTAT | 23603 |
rs372562944 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671831 | ACAGTGGCACGATCA[C/T]GGCTCAATGCAGCCT | 23603 |
rs372573155 | snp | A/G | 0.000282174 | 0.0118747 | intron-variant, missense | CORO1C | GRCh38.p7 | 12:108657443 | AGAGCAAAAAGGCAC[A/G]TGCCACACATTAAAC | 23603 |
rs372617852 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712481 | CAGGAGGCTGAGGCA[C/T]GAGAATTGCTTGAAC | 23603 |
rs372626303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727981 | TGTTCACCAACCACA[C/T]GAAAAGATGCTCAAC | 23603 |
rs372636316 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684150 | ACACAAGCAGAGAAC[A/T]CACAGCGAAGAAAAT | 23603 |
rs372664597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689776 | ATTTTAGGAAAAAAT[A/G]AGTATCAAAATCACT | 23603 |
rs372674296 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726292 | GGTGTAGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 23603 |
rs372691729 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662558 | CAGCTTTTATTTAAT[A/G]TTATTTGGGATTTTA | 23603 |
rs372693521 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108686554 | AAATTGAAGTAGTTT[A/G]GCTGAAAATGTAATA | 23603 |
rs372724972 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696042 | ACAGTTGTGTATAAG[A/G]AAGTACCACACAGCT | 23603 |
rs372909353 | snp | A/G | 8.2543e-05 | 0.00642376 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662072 | TGGATGCCAAGCCAC[A/G]ATGCCGACTCTCTTT | 23603 |
rs372931772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671166 | TGTGAGAAACCTCGT[C/G]TCTACAAAAAAAATA | 23603 |
rs372937354 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683418 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23603 |
rs372988394 | snp | A/G/T | 3.36929e-05 | 0.00410433 | intron-variant | CORO1C | GRCh38.p7 | 12:108657276 | AAAGCTCAAGTGAAA[A/G/T]CAAGTGGAAAGCCTG | 23603 |
rs372991808 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655418 | CCCTCTCTTTCCACG[C/G]TCTCCCTCTGATGCC | 23603 |
rs373000094 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703522 | CACGTGTAACTGACT[A/G]AAGTGTGAGTGTCCT | 23603 |
rs373022360 | snp | C/T | 0.000148585 | 0.00861802 | intron-variant | CORO1C | GRCh38.p7 | 12:108648939 | TGTTTAAAATATGGA[C/T]TGTCTAGAAAACTCA | 23603 |
rs373023923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108693798 | TTAACAGTTTAAAAG[C/T]TGGGTTGGCTCCTCT | 23603 |
rs373025876 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655953 | CGTCTCTGCCCGGCC[A/G]CCCATCGTCTGAGAT | 23603 |
rs373098449 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672250 | GAGAGTACTTCAATG[C/T]AGTTACTCACAGAAC | 23603 |
rs373124654 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729433 | TAATGTACCTTCCAC[A/G]AGTAATCAAAATAAA | 23603 |
rs373130051 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715670 | TACTCACAACACTGG[A/C]AGCAGCCATCTCCCT | 23603 |
rs373130369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108660189 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 23603 |
rs373175112 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703510 | AAAGCTGTCATGCAC[A/G]TGTAACTGACTGAAG | 23603 |
rs373205541 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108681719 | AAATTCTTAGATTTG[C/T]CTCAAAGAATTGCTA | 23603 |
rs373223996 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696778 | GTGGCAAGCCACAGC[A/T]TGATGGAAGCATTAC | 23603 |
rs373244113 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108720148 | CCTCAATCACACCAC[G/T]GCACTCCAGCCTGGG | 23603 |
rs373260407 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683445 | AAAAGAGGAAAAAAA[G/T]AAGTCAGTGGAAAAA | 23603 |
rs373375625 | in-del | -/AG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722985 | GCCCACAGAAGAGAG[-/AG]CCTAAAGGACAGTTA | 23603 |
rs373477385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108661241 | CCAATTTTAGATAAA[A/G]GAAAAGATTTCTGTA | 23603 |
rs373525820 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660580 | CCCTATAGGCAAACA[-/A]GGTAACTTCAGCCCC | 23603 |
rs373541910 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659435 | CTATAGAGAACATAT[A/G]TAAACAAAAGGAAAA | 23603 |
rs373612252 | snp | A/C | | | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701180 | CCTCTATGATTATGG[A/C]AACAAATCTGGGATT | 23603 |
rs373691988 | snp | C/T | 0.000197997 | 0.00994783 | missense, utr-variant-5-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701323 | ACTCGCCTCATCGTG[C/T]CTGCAAAGGAAGAGT | 23603 |
rs373716377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108725643 | AGAACTACAGAAGGT[A/G]CCCATAGCTCACTGT | 23603 |
rs373745426 | snp | A/C | 3.45399e-05 | 0.00415557 | intron-variant | CORO1C | GRCh38.p7 | 12:108647568 | AAAATGCAGTAAACA[A/C]AGTTCAACACTGTTC | 23603 |
rs373787461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108692335 | AACACCAAAGCTACC[A/G]AGTGCCAAATGTCCA | 23603 |
rs373789758 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108666515 | TGCTCACAGGCCTGT[C/T]ATTATGTGGCTCTCT | 23603 |
rs373799043 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712214 | CAGGTAAGACAGCAG[A/G]TGAGGAGACAAATAT | 23603 |
rs373842865 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675502 | ACGGGGAAAAAAAAA[-/A]CCCTAATTTGTCACC | 23603 |
rs373856742 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709849 | GAAAAACTGCTTGCT[C/T]ATTAGGTCTTTCAAG | 23603 |
rs373960341 | snp | G/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732841 | CACAGGGTTCCATGA[G/T]ATCATATTAGCAGCC | 23603 |
rs373988968 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684903 | CCAAGGAAAAAAGCT[G/T]TTCTACCTGAATTGT | 23603 |
rs374057495 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703717 | CAGATCCCAGGGCTG[C/T]ACAACCAGGGTACTG | 23603 |
rs374081311 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706384 | AAGATGAGCTTGTCC[-/C]ACCCTTGCCACTTCT | 23603 |
rs374158227 | in-del | -/A | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108679186 | AAAAAAAAAAAAAAA[-/A]GAAAAGCTTTAGCTA | 23603 |
rs374194310 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722148 | AGACAATCTGTTTAT[A/C]AGTAAGGAACCTCCT | 23603 |
rs374244314 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CORO1C | GRCh38.p7 | 12:108662011 | GACAAGGGGAGGACC[A/G]CTGAGCTCAGCTCCC | 23603 |
rs374279806 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716812 | TACTTACTAACATCC[A/T]CAGGGTTATACGTAT | 23603 |
rs374284824 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679026 | TGAGGCAGGAGTATC[A/G]CTTGAACCCGGTAGG | 23603 |
rs374286308 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645683 | ACATGGTCCTTTTTC[C/T]ACACGGACATTACTC | 23603 |
rs374294256 | snp | C/T | | | utr-variant-5-prime, intron-variant | CORO1C | GRCh38.p7 | 12:108702984 | AGATGGCAAATGATT[C/T]GTGGCCAGGGTCCTT | 23603 |
rs374333199 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697318 | TGCCTGTCTATAACC[A/G]GAAACAAAAAAGGGA | 23603 |
rs374350794 | snp | A/T | 1.6755e-05 | 0.00289435 | intron-variant | CORO1C | GRCh38.p7 | 12:108652464 | ATTGTTAACTGAAAC[A/T]TCTGGATTATGGGGG | 23603 |
rs374356149 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684173 | AAGAAAATCTGAAGA[C/T]GCAATAGATGTGTGA | 23603 |
rs374356356 | snp | A/G | 0.0134861 | 0.0810011 | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645258 | AAAAAAAGACAAAAC[A/G]GGAAAATAATCCACA | 23603 |
rs374363703 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108709923 | GTAAGATCATCTCAG[C/T]AATAAAGAGGAAGAC | 23603 |
rs374367983 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108675641 | TAAATAGTAAGTAAG[A/T]GAGGACATTATCTTA | 23603 |
rs374370041 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699179 | TAAAGAATGAAATAC[A/G]AGGACACATTCATTA | 23603 |
rs374388755 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687535 | CACGCCTGTAATCTC[A/C]GCACTTTGGGAGGCT | 23603 |
rs374440874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662262 | TCTATGTAAACAGAA[C/T]ATAGAGTGATATCTG | 23603 |
rs374447417 | snp | A/C/G | 1.65425e-05 | 0.00287593 | intron-variant | CORO1C | GRCh38.p7 | 12:108649033 | AATCTTCAGAGGGGA[A/C/G]ATAAAGGCAAAGTTG | 23603 |
rs374457050 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651933 | GGAAGGCTAAGGCAG[A/G]AGAATTGCTTGAACC | 23603 |
rs374469222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108718669 | TAGCGCTTACAATCT[C/T]ACTGCACCTTAGGAA | 23603 |
rs374475355 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | CORO1C | GRCh38.p7 | 12:108720624 | TGTCTCCGAGTTCAT[G/T]CCATTTTCCTGCCCT | 23603 |
rs374484534 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659019 | CACATATGTATATGC[-/AG]AGAGAGAGAGAGAGA | 23603 |
rs374509304 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705161 | TCAGTTTCCCATTCA[C/T]AAAATGAAGGGAATG | 23603 |
rs374690575 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695173 | AGCTGGTGCTGGCAG[G/T]CATCAGGAGGTCCTA | 23603 |
rs374804989 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108678471 | CTCAGGCCCATTTCT[A/C]ATTTATTACCTCCAC | 23603 |
rs374814179 | in-del | -/CT | 0.021333 | 0.101051 | intron-variant | CORO1C | GRCh38.p7 | 12:108701013 | ACTTCAATTACATCA[-/CT]GAGTCTAATGGTTTC | 23603 |
rs374868395 | snp | G/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648738 | GGAATGTACCCGTGC[G/T]TCAAGGAGATGAGGA | 23603 |
rs374885206 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672015 | CCGTCCACCTGCCTC[A/G]GCCTCCCAAATTGCT | 23603 |
rs374889542 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699996 | AAAAGTCCAAGAGAA[C/T]TGGACATTTTCCCAA | 23603 |
rs374908445 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728687 | AGTACAGAATCTTGT[G/T]CACTCACTTTAAAGG | 23603 |
rs374944087 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703031 | TGAATACTTCTCAAG[C/T]GTGAGTTAGATAAGA | 23603 |
rs374947613 | snp | A/G | 4.95855e-05 | 0.00497899 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662055 | AGCACATTGCGGGCC[A/G]TTGGATGCCAAGCCA | 23603 |
rs374947660 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730536 | CTGACCTCATCCTCA[A/G]TCATTTCGGCGCAGC | 23603 |
rs374957897 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714465 | AGAAACACACACACA[C/T]ACCCCAAGGATAGTA | 23603 |
rs375018209 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669700 | AAAAAAGGCGGGGGG[G/T]GGCGGGGGGTGTTGT | 23603 |
rs375038851 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648776 | TGCATTCTTGCCTTC[A/G]AACCACTCTTCTGCC | 23603 |
rs375042948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108682370 | CAAATAAAGGAGGGC[A/G]GCATATTAAAAAGTA | 23603 |
rs375063128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654133 | ACTGGCAAGCTGCAC[A/G]CAGTCCAGTCTCAAG | 23603 |
rs375105000 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108727273 | AATACATGAGGGCAG[A/G]GACAAATGTCTGCCT | 23603 |
rs375124692 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698394 | ACATGATCTAGAATT[C/T]CCAAGGCAGAAAATA | 23603 |
rs375125043 | snp | A/C/T | 3.29523e-05 | 0.00405898 | intron-variant | CORO1C | GRCh38.p7 | 12:108648590 | CAAGCACCCCTGCAC[A/C/T]CCACTGGTCCTCACC | 23603 |
rs375128764 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648386 | GCCACACTTGGCTCC[C/T]TTAATGGGGCTAAAG | 23603 |
rs375153969 | snp | A/C | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658452 | CAATTGGTTTAATTG[A/C]TCAAGACTTATAAAC | 23603 |
rs375172317 | snp | C/T | 1.68749e-05 | 0.00290468 | intron-variant | CORO1C | GRCh38.p7 | 12:108678258 | TGTGTGCACACAACA[C/T]CCTGGGAGCTTACCA | 23603 |
rs375213412 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700927 | GGCATCCCCAGAACA[C/G]AGGTCACTATTCTAT | 23603 |
rs375229600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108647701 | GAATGCAATGAGCAC[C/T]GGCCGATCTATCTGA | 23603 |
rs375268621 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679382 | TAGCTACCACAATTT[C/G]CTCATGTCACACATT | 23603 |
rs375316576 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705528 | CAGACCCAGATGACT[C/T]CACTGCTAAAGTCTA | 23603 |
rs375426539 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699624 | CCCCTTGCTCTTGGT[A/G]AAGGAATAAGCTAAA | 23603 |
rs375429071 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723023 | TTCTAAAACAGACAA[C/G]GTGCATCTTATTAAA | 23603 |
rs375508697 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679156 | AAAGAAAAAAAAAAA[A/G]AAATTTAAAAAGTTA | 23603 |
rs375773465 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722072 | TGCCTGACTTCACAT[G/T]CCTCTGCTCAACTTT | 23603 |
rs375777136 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664710 | GGCATCTGCTCTCCT[C/G]CATTACTGCATGTTA | 23603 |
rs375805992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108660348 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 23603 |
rs375858233 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694799 | CTACGTAGATTTTTT[C/T]CTTAAAGGCTAGGTG | 23603 |
rs375897817 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108712609 | GAAGTGGGAAATGTA[A/G]TAATATATAAGCCTA | 23603 |
rs375915126 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660419 | TCATGCCATTGCACT[C/T]CAGCCTGAGCAACAA | 23603 |
rs375971703 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723868 | TCTGGCAAGATGCAA[C/T]GCAAGGGCACCTTTG | 23603 |
rs375999412 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712287 | TTCCTTTTAAGAAGA[C/T]GGAGGCCGGGCAGGG | 23603 |
rs376036155 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687442 | CAGTGAACTATGATC[A/G]CGCCACTGCACTCCA | 23603 |
rs376097106 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693854 | GAGGAAAAAAAAAAA[-/A]CCTGAATTCAAACCG | 23603 |
rs376117125 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716817 | ACTAACATCCACAGG[A/G]TTATACGTATTACAT | 23603 |
rs376175373 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673380 | GAAGCTGCAGAAGAA[A/C]AGTTGGAAACTAGCA | 23603 |
rs376364526 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665669 | AGAGAAAACATTAGT[A/T]CCTATGCCTGCGAGG | 23603 |
rs376380472 | snp | C/G | 1.66563e-05 | 0.0028858 | intron-variant | CORO1C | GRCh38.p7 | 12:108657460 | GCCACACATTAAACT[C/G]CAAGAAGACAAGGTG | 23603 |
rs376424200 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108653228 | CTAGTCATTTCTGCA[C/T]GCCCAAAAGAATTTT | 23603 |
rs376455923 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722776 | CTTGCTCATTCACTT[G/T]CAGAGAAACACACAG | 23603 |
rs376458929 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652386 | TACGGGGATTCATCC[A/G]TGATCTCAAAATAGC | 23603 |
rs376462840 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652050 | AAGTGAGATTTTTTT[C/T]TTTTCTTTTTTTTTT | 23603 |
rs376577025 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727857 | CAGCTGATAAGGCAC[G/T]TGAATCTAGAATACA | 23603 |
rs376582826 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670799 | ACATGCTCAAAAGAG[A/G]TAAAAACTACATTAT | 23603 |
rs376683963 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108715642 | CCTCCTCCCTCCCCC[C/G]CTCCCCCCCGCATAC | 23603 |
rs376689544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108684314 | GACAAGGATGTCAGG[A/G]AAGAGGAACTCATAA | 23603 |
rs376835118 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664486 | TAAATTCTGCCCAGG[C/T]TAAATATAACCCCTT | 23603 |
rs376840207 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683286 | TAGCCAGGCATGGTG[A/G]TGGGTGCCTGTAATT | 23603 |
rs376884358 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647681 | CCTACTATGTCTGGG[A/G]CTTTGAATGCAATGA | 23603 |
rs376900952 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667847 | TTTCACATGTGAAAG[C/T]CTGGATATGGAAAAA | 23603 |
rs376905579 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108707094 | CAGAAGACTTAGCAT[A/T]GAGATGGCAATATTC | 23603 |
rs376985274 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689340 | ATGTTTTCACAAAGT[A/T]ATAAATTCCCATGGT | 23603 |
rs376996109 | in-del | -/ACAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664024 | AAGGTTAAGAAACAA[-/ACAA]CCTCTAAGAAAAGGG | 23603 |
rs377059726 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700333 | TCACAGCTTTTTTTT[-/T]CTTCATTATTTGCAG | 23603 |
rs377069697 | snp | A/G | 8.30862e-05 | 0.00644486 | intron-variant | CORO1C | GRCh38.p7 | 12:108662190 | AAAGATGATCCACAT[A/G]AAAGCTATTGCCTTT | 23603 |
rs377132460 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CORO1C | GRCh38.p7 | 12:108654429 | GGGGGAAGATAATAA[C/T]AATACATATATGTGT | 23603 |
rs377135365 | snp | C/T | 8.30213e-05 | 0.00644234 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658709 | CTCAAGTGCTCCAAC[C/T]ACTGAGTTTTCATCC | 23603 |
rs377141389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108714157 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 23603 |
rs377146727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688962 | CTTGAGCCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 23603 |
rs377159265 | in-del | -/CAGTGGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683450 | AGGAAAAAAAGAAGT[-/CAGTGGA]AAAAAAATAAATAAC | 23603 |
rs377184446 | snp | C/T | 3.30033e-05 | 0.00406209 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654357 | ATAGAAAGGCAGCAA[C/T]ACCCCATTGCTAGTG | 23603 |
rs377185786 | snp | C/T | 0.000131941 | 0.00812116 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657390 | GGAAGATGGCTCTCA[C/T]GGGTCTTGCTCCTTC | 23603 |
rs377224378 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108709773 | TAACACAATAGGCAC[-/A]AATTCCAAGGAAATA | 23603 |
rs377235373 | in-del | -/ATTT | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658188 | CTTTTCGCCCTGCGC[-/ATTT]ATTTATTTATTTATT | 23603 |
rs377270206 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689032 | TGAGACTCTGTCTCA[A/G]AAAAAAAAAAAAAAA | 23603 |
rs377338244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720681 | GGCGCCCGCCACCAC[A/G]CCCGGCTAATTTTTT | 23603 |
rs377349454 | in-del | -/AC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696421 | GGGGGGAGGGAGGGG[-/AC]GGGGGGGTTGTATGT | 23603 |
rs377402125 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673258 | ACAGCCTTGTTTTAG[C/T]GGTCTGGATAGAAAT | 23603 |
rs377504365 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | CORO1C | GRCh38.p7 | 12:108701097 | TATCAGAGGGTGTCT[A/G]CCAGAATGGAAGATC | 23603 |
rs377507442 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108651277 | ACAAATGTTTGGTAC[A/G/T]ACCTTATATGTGATG | 23603 |
rs377508895 | snp | C/T | 6.60611e-05 | 0.00574684 | intron-variant | CORO1C | GRCh38.p7 | 12:108648935 | CATTTGTTTAAAATA[C/T]GGATTGTCTAGAAAA | 23603 |
rs377569941 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647484 | GTCTTTTATAGATTT[A/G]ATCTCTTTTAAAATC | 23603 |
rs377594652 | in-del | -/CAGGACGAGTGCC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721771 | GAATAGAAAAATAGA[-/CAGGACGAGTGCC]CAGCTCTGGCCATTA | 23603 |
rs377595816 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666814 | GGTTATTAGAAGGGT[-/T]AAATGAGCTCAAACA | 23603 |
rs377694610 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108685084 | ACACAAAGCAATTTT[-/G]AGGGGAATCTGGAAG | 23603 |
rs377704534 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655725 | GGTGTGATCTCGGCT[A/G]GCTACAACCTCCACC | 23603 |
rs377708814 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697607 | CTTTTCCAGGGTAAA[A/G]AGCCCTAGTATTACA | 23603 |
rs377712050 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708519 | CAGGCTGGAGTGCAA[C/T]GGCTCAAACTCGGCT | 23603 |
rs377716541 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108672400 | AACTAAAAGTCGTTT[A/C]GTTTTTTAACGATTT | 23603 |
rs377730492 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108674820 | AAAGAAAATGGTCTC[-/TT]GAGATGGAATGTACT | 23603 |
rs377732766 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646006 | CCTCTGTGCTTTGAC[A/G]CAGCCTTGGTGAGAG | 23603 |
rs377742245 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702005 | GTACACAGTGAGAAA[C/T]AGGAAAAGTCAGCCT | 23603 |
rs377765869 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703082 | AAAGCAAAAGGAAAG[C/T]ACATCTATACAAAAG | 23603 |
rs377767099 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108725981 | AGCTGGGACTACAGG[C/T]GCGTGCCACCACACC | 23603 |
rs386377698 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679171 | AAATTTAAAAAGTTA[-/A]AAAAAAAAAAAAAAA | 23603 |
rs386766259 | in-del | ATGCCAGT/CACAGACCTAAGGGCACCAATACCAGGCACTGAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652846 | TAACGCAATGCTGTT[lengthTooLong]ATGATGATAAAAAGT | 23603 |
rs386766260 | multinucleotide-polymorphism | ACA/GCG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667070 | AAGGCTTAGAATAGC[ACA/GCG]TGGCAAAAAAAAAAA | 23603 |
rs386766261 | multinucleotide-polymorphism | AG/GA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674443 | GTCCCAGCTACTCGG[AG/GA]GGCTGAGGCAGGAGA | 23603 |
rs397753962 | in-del | -/A | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108694799 | CACCTAGCCTTTAAG[-/A]AAAAAATCTACGTAG | 23603 |
rs397935171 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704485 | CAAAAAAAAAAAAAA[-/A]GTTATTTCCATATTA | 23603 |
rs397949163 | in-del | -/GAGG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647956 | CTGCCATCTGTGAGG[-/GAGG]CTCCTTCTTGGGAGG | 23603 |
rs398021003 | in-del | -/A | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108692815 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 23603 |
rs398021004 | in-del | -/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108716158 | AAACATATTCAAGGA[-/T]TTTTTTTTTTTTTTT | 23603 |
rs527246620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677244 | CTAACCTTTTCAGCC[C/T]ACTTTGGGCTAGCAT | 23603 |
rs527293061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684579 | CGCGAAATAAAAGTA[C/T]ATGTTACAGATAAAC | 23603 |
rs527326863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730539 | ACCTCATCCTCAGTC[A/G]TTTCGGCGCAGCGGG | 23603 |
rs527375399 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108669990 | TTTAATTTACAAAAT[C/G]TGCACTCCAGCAATG | 23603 |
rs527387325 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731187 | GCTTCACGCTCCCCA[C/G]GCCACCTGGTTCGGT | 23603 |
rs527411252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677912 | TAATCCCAATTACTC[A/G]GGAGGCTGAGGCAGG | 23603 |
rs527495474 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661485 | TTCGGAAAGAAACAT[C/G]AAAAAAGTAATAATG | 23603 |
rs527496589 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723752 | AGTGGTTTTCATTAT[-/G]TCTGTTACAATCTAT | 23603 |
rs527515664 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108653835 | ATCCACAAAGCACCA[C/T]TCTCCTTCCAAGTCC | 23603 |
rs527515941 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645822 | GTGGTCCCAATGGCA[A/C]TACACATTTCACGTT | 23603 |
rs527532294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108709807 | GGTATGATTTTAAAT[A/G]TCCTGTCAGAGAGTG | 23603 |
rs527563788 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728379 | TACAATACTACCACA[C/T]ATATAAACCTTGAAA | 23603 |
rs527606176 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646212 | CAGGAAGGAAAGAAG[G/T]AATGGCTGGGGGAGC | 23603 |
rs527623058 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688459 | TCCCAAACTCTCGAA[A/G]TTCAACATTGGGAAT | 23603 |
rs527741062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706533 | TATACAGAAAATCCC[A/G]AGGAATCCACTAAAA | 23603 |
rs527799911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660177 | AGGAAACTGGCCGGG[C/T]ACGGTGGCTCACGCC | 23603 |
rs527849299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682834 | CATCTTCTGAGTATA[A/G]TGCAATACAATTAAA | 23603 |
rs527854296 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680430 | AAATTCCAATGAACA[C/T]CATATCATATAGAAT | 23603 |
rs527951148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720848 | ATTAGTAGTCCTAGG[C/T]CATAGAAAACATCTT | 23603 |
rs527953036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108729545 | CACGACTAACCTCCA[C/T]CACGAAACACTGCAC | 23603 |
rs527970637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667523 | AATTTAAATAATGCT[G/T]TGTGTTCCTAACATT | 23603 |
rs528068305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108705802 | GATTTATCCTAGGAA[C/T]GCGAGGTTGGGTCAA | 23603 |
rs528070549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696813 | GAGAGTGGGAATCAC[A/G]TGTGCTAATCTAAAT | 23603 |
rs528103786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108671883 | TCCTCCCACCTCAGG[C/T]TCCCAAGCAGCTGGG | 23603 |
rs528105934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705089 | CTGACATAAGATAAT[C/T]TGGATTCAAATCTGA | 23603 |
rs528229679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689630 | TACACCACCCGAAGA[C/T]GTAAGGGCCTAAGAG | 23603 |
rs528233156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697528 | TTCTTTGCCTTTAAA[C/G]CAAAGCAACACCTCA | 23603 |
rs528242547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664914 | AAATGGGACTTCAGT[A/G]ACTCAACAGGAAAAG | 23603 |
rs528284281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711780 | TTTATATTGCAACAG[C/T]ACCAAATAAAATACA | 23603 |
rs528306082 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108727885 | ACATGAACAACTTTT[A/G]TAACACCAATAAAAA | 23603 |
rs528373051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658428 | AAGCTGCAAAATCAG[A/G]AATGCAGCCAATTGG | 23603 |
rs528396437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657844 | TAACGCTTTCCTTGA[C/T]CTCAGTAGTTTAATG | 23603 |
rs528462769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680224 | ACAGAGAAGGAAGAC[A/G]TTCAAGCAGGTTTGT | 23603 |
rs528477532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695871 | AAAAAAAAAAAAAAA[A/C]AAAACAGTCTTTCAA | 23603 |
rs528604260 | snp | C/G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666187 | ATAAAACACGCAGAT[C/G/T]TGTAGAGCAATTTTC | 23603 |
rs528641315 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725398 | GTACCTACTCTGTAT[C/T]AGGCACTTCATATAA | 23603 |
rs528676504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710784 | GGCCAAGATGGTCTC[A/G]ATCTCTTCACCTCAT | 23603 |
rs528732706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656893 | CCTAATCTCAAGTAC[A/C]CAGGGACACAAACAC | 23603 |
rs528818233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108695057 | GGTGGCTCTGGCCCA[A/G]GGTTTTTCACGAGAT | 23603 |
rs528818754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649091 | CAGGATGAATAATTA[C/G]TTTTCTACAATGCTG | 23603 |
rs528876350 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108690738 | ATTCCATATGATGCT[C/T]CTGGGCTGAGAACAA | 23603 |
rs528916633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697772 | ACACAAGTGCTCCTG[A/G]AGGGCACAGATGCTG | 23603 |
rs529034599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682938 | AAAAATCATAATGGA[C/T]AACAGAATGAAAGTT | 23603 |
rs529075393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108713189 | CAAAATGTCAGATAC[A/G]CAACAGATCTCCTCA | 23603 |
rs529082221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108720651 | CCCTCAGCCTCCTGA[A/G]TAGCTGGGACTACAG | 23603 |
rs529096588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688738 | ACGGTGAAACTTCAT[A/C]TCTACTAAAAATACA | 23603 |
rs529100364 | in-del | -/T | 0.389903 | 0.207189 | intron-variant | CORO1C | GRCh38.p7 | 12:108687924 | TATCCCCTCTGACCC[-/T]TTTTTTTTTTTTTGA | 23603 |
rs529120287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712442 | AGGTGGGCGTGGTTG[A/C]AGGTGCCTGTAATCC | 23603 |
rs529194080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108651469 | AATTATATCATAGCT[A/G]AACTTCCTAAATCAA | 23603 |
rs529260496 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651434 | TTTTCTAAAAATCAG[A/T]AGTAGTACAGAGAGG | 23603 |
rs529295652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680835 | TATTGCATTCTCACA[A/G]AAATCATGCAGGTAA | 23603 |
rs529348565 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645046 | AGTCAGAGAAGCTAT[A/G]TCAGGCAGAGAGGTG | 23603 |
rs529388141 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690790 | TGAGGTAGAATCTAG[C/T]TAAAATAAAATTGAG | 23603 |
rs529402125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674522 | CACTGCGCTCCAGCC[C/T]GGGCGACAGAGCGAG | 23603 |
rs529412797 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717132 | GAGAAGCGACACTTA[A/G]GCTGAAATCAAAGAA | 23603 |
rs529432306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696133 | TGGCCATACCCATCC[G/T]ATCCTGGCCAGAGCA | 23603 |
rs529452121 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721346 | GTCAGCCCAGTACTA[C/T]TAGGCACACCCTCAG | 23603 |
rs529512869 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108696086 | CATGGGAGAGAAGAA[-/T]GAGATCATGACCCAA | 23603 |
rs529599680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663836 | TCTATGTGAATTATA[A/T]CTCAATAAAACTTGT | 23603 |
rs529623209 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680720 | CTCAATAAACATTAC[A/C]CGAAATTTAACAAAT | 23603 |
rs529659274 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654102 | AGTATGCAACATGGC[A/G]TGTTATCACTGCACA | 23603 |
rs529702179 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703177 | AAGTTATAGAAGCTG[C/G]AATCCCTACCAGCAT | 23603 |
rs529715930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108711635 | CAGTGAACCGAGATC[A/G]CGTCACTGCACTCCA | 23603 |
rs529717905 | in-del | -/AGTA | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108675631 | ATTTGGTAACTAAAT[-/AGTA]AGTAAGTGAGGACAT | 23603 |
rs529722456 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653688 | GTTTTTGGAGTTCAG[C/T]GTGGAGTCTCCCTAT | 23603 |
rs529747139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657620 | GTCAAGGTCCCTCTG[G/T]GAGGCTGCAAGAATG | 23603 |
rs529750109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717875 | TATGTACTTTTGCTC[A/G]CAAAAGTGTCTGGAG | 23603 |
rs529777693 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678177 | ACGTTCTGCTTTTCA[A/C]GCCTCTATACATACA | 23603 |
rs529792253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649201 | GACAGATGAGAGAAC[A/G]GAAGCTGAGAGTCAC | 23603 |
rs529801525 | in-del | -/T | 0.406814 | 0.194704 | intron-variant | CORO1C | GRCh38.p7 | 12:108720525 | ATAACATAATAAGAA[-/T]TTTTTTTTTTTTATT | 23603 |
rs529802738 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108657058 | AATAAAATTAAAATT[A/T]AAAAAAATTAAAAAA | 23603 |
rs529901712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707377 | TAAAGTCCAGAAGTA[A/C]ACTCATACATCTTTG | 23603 |
rs529919033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717224 | TATCAAAAGTCTGTA[C/T]CAAAAGCAAGCACTT | 23603 |
rs529931748 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108672668 | TTTTGTTTTTTTTTT[A/T]AAACAAATTGAAGCT | 23603 |
rs529932218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663298 | ATGATTAAACAGAGT[C/T]ATCATATGATCCGGT | 23603 |
rs529956753 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733038 | TTATTTTGCCTTCAA[C/G]CAGCCACTCCTAATA | 23603 |
rs529969691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671859 | CCTTGATCTTCCAGG[C/T]CCAAGAGGTCCTCCC | 23603 |
rs529981978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108726280 | AAAAATTAGCCGGGT[A/G]TAGTGGCGGGCGCCT | 23603 |
rs530019095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108725866 | CCCAGGCTGGAGTGC[A/G]ACTCTGTCGCCCAGG | 23603 |
rs530069070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647625 | TTTCTATTTTGCAAA[C/T]GGCAAGCCATAGTCA | 23603 |
rs530101756 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108693763 | CTTTGCCCTCCTAGG[A/G]ACAGAGCCCCTCTAC | 23603 |
rs530101757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108702212 | GTAAACCAGACTTGA[A/G]GAAGGCCTGGAGTGA | 23603 |
rs530153993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648424 | AACTCCGTTAAAGGA[C/G]GCAAGTGTTGCCACA | 23603 |
rs530163017 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645915 | TAAGAAACTGGAAAC[A/G]GGGCAAAGTTCCAGC | 23603 |
rs530264264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694042 | GCTCACGCCTGTAAT[C/G]CCACTTTGGGAGGGC | 23603 |
rs530272069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670806 | CAAAAGAGATAAAAA[C/T]TACATTATAGTGATT | 23603 |
rs530334693 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108654892 | TGTATTTTTAGTAGA[C/T]ACAGAGTTTCACCAT | 23603 |
rs530417277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655591 | TTCGCTGTGTTGGCG[A/G]GGCTGGTCTCCAGCT | 23603 |
rs530432796 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646489 | TTGTCAAGTATTGAC[C/T]AAAACCTGAAACATG | 23603 |
rs530440704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662276 | ACATAGAGTGATATC[C/T]GGATGAAAGGCAGAA | 23603 |
rs530460461 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698721 | CAGAAAATAACTTTT[A/G]TACACAGCTGCTTAT | 23603 |
rs530511017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108651259 | ACATAAACACAGTGT[C/T]ACACAAATGTTTGGT | 23603 |
rs530551741 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704329 | ATACAAAAATTAGCC[A/G]GGTGTGGCGGCAGGC | 23603 |
rs530576218 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732253 | CCTGAACCGTCCATT[C/G]TCACATTCCTAGTGC | 23603 |
rs530712891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664687 | CTCTTTCCCCTGCGG[A/T]GAACATGGGCATCTG | 23603 |
rs530717757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718006 | GTGGATCACCTGAGG[C/T]AAGGAGTTCAAGACC | 23603 |
rs530742140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680023 | GTCACATTATTAGTT[C/T]TTCTAGTACAATAAT | 23603 |
rs530779728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710985 | GCAATAAAACCTTCA[C/T]CTTATTAGTCAGGTG | 23603 |
rs530783631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108719014 | AACATTTGGGCTAAA[C/T]ATTCTAAGAGCAAAT | 23603 |
rs530982059 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694900 | AACTAACATTATGAG[C/T]CACGTAATACAGTCT | 23603 |
rs530991776 | snp | A/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701133 | ACCTACCTTGTGCAG[A/T]GGGAGGACAAGGAAC | 23603 |
rs531041365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717115 | GGGAACAGAAGCAGT[C/T]AGAGAAGCGACACTT | 23603 |
rs531075128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688338 | TAATGTACACAAACA[G/T]GTACAGAAAATTTCT | 23603 |
rs531085440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663149 | ATTAGGATGGCTAGA[A/G]TCAAAAAGACAGATA | 23603 |
rs531112642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647686 | TATGTCTGGGGCTTT[A/G]AATGCAATGAGCACT | 23603 |
rs531180344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670080 | TTTTGGGGGTTTTTC[C/T]GAAGTCCCTCCGTAA | 23603 |
rs531194155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702485 | GATCACCAGGCCCTC[A/C]CTGATTAAGATTTCC | 23603 |
rs531228040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648535 | ACTCGCCGACGCCCT[A/G]GACCACAAGGGCTTT | 23603 |
rs531235061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108656322 | CGGCCAGCCGCCCCG[C/T]CCGGGAGGGAGGTGG | 23603 |
rs531239458 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108724027 | AGAAATCAAGTTTAC[A/C]AAAGGTTTATCCAAG | 23603 |
rs531266239 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728430 | ACACAAAAGACCACA[C/T]AGTGTATGATTCCAT | 23603 |
rs531291594 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108707665 | TTTATAAACTTTATG[C/T]CTCAAAGGACACTAT | 23603 |
rs531351632 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658477 | ATAAACTCTTAAGGA[C/T]TCTAGTGAACTGATA | 23603 |
rs531379936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108726129 | TGAGCCACCACGCCC[A/G]GCATGAAATATTTTT | 23603 |
rs531422740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692203 | GCTTTTCACGGCCCA[C/T]ACACTTGGCAGTTGA | 23603 |
rs531431418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662336 | TTTTTTTGTTTGTTT[G/T]TTTGTTTTTTGTTTT | 23603 |
rs531476496 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731351 | GCTCCTGTCAGGCGG[A/C]GCAGGCACATGCTCA | 23603 |
rs531541868 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CORO1C | GRCh38.p7 | 12:108656585 | ACGGGCCATGATGAC[A/G]ATGGCGGTTTTGTGG | 23603 |
rs531556161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660821 | AAAATGATTCCCAAG[C/T]ATAGTCGATGGTGAT | 23603 |
rs531565419 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646914 | CCTTTCAAATTAAGG[A/G]AAAAAAACCACACAC | 23603 |
rs531602415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707353 | ACATTTATATCAATG[A/G]AATATAATTAAAGTC | 23603 |
rs531669713 | in-del | -/GGCC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711397 | CAAAAGAAAGAAAAG[-/GGCC]GGCCGGGCATGGTGG | 23603 |
rs531679973 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681645 | AAAAAAGCAAACAAA[A/G]GGCACTGCAGACAAA | 23603 |
rs531702326 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646435 | GAAAAGGGCAAGAAG[A/G]AACACTCAGCAGTAC | 23603 |
rs531715938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108653965 | CAGATAAATCTAAAA[C/T]CACCAATCAGGTAGC | 23603 |
rs531743774 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712174 | AATGTAGAAGAGATC[C/T]GATGTGTTATTCAAT | 23603 |
rs531781424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108676542 | TTTGGGAGGCTGAGG[C/T]GGGGGGATCACTTGA | 23603 |
rs531789922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108708230 | TAGAAGCAACCCAAA[C/T]ACAGACTATCCATTG | 23603 |
rs531830266 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650231 | TCTTGCTCCATCGCC[C/T]AGGCTGGAGTGCAGT | 23603 |
rs531853274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108729654 | AATGTTTACTATTAT[A/G]CTTCATAGCCAAACA | 23603 |
rs531902776 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661844 | CTTGAAACACACACA[C/T]GTGCACACACACACA | 23603 |
rs532037401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730451 | ATCATTTGAGAGACG[C/G]AGAGCTGGGGAGCGT | 23603 |
rs532048737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722013 | AAGCAGGCATGGTTT[C/G]TTCCTGATTCCAGGT | 23603 |
rs532058403 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685636 | AAGGCACACAAGTAA[G/T]GTTAAAAATTATTGG | 23603 |
rs532063740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677036 | TTTGTATTTATGTAA[A/T]ATAATTTTAATTAAT | 23603 |
rs532076642 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649414 | TTGTATCTACAACGC[A/G]GGTACAAGGTCTTCT | 23603 |
rs532085250 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671782 | TATTTATTTAGAGAC[A/C]GGATTGGTCTCACTC | 23603 |
rs532106177 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721406 | CACTGACTCTCCAAC[A/G]CCTGTCTCCTGAATT | 23603 |
rs532122373 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108717195 | GTGAGTCCCAGCTGG[C/G]AGGAACAACAAAATA | 23603 |
rs532138115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686892 | AATTCAGCTTCCAAA[A/G]CATGTATACAGCTGG | 23603 |
rs532155661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684275 | CAAAACTGGTGAAAA[C/T]GTAAAAGTATAAATA | 23603 |
rs532192031 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717304 | GGGTAGAAGAGGCTG[C/G]GAGGTCAGCAGAACC | 23603 |
rs532211076 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704414 | TAGGCGGAGGCTTCA[C/G]TGAGCCAAGATCGCA | 23603 |
rs532244165 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108656368 | CCGGCCAGCCGCCCC[A/G]TCCGGGAGGGAGGTG | 23603 |
rs532261798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679152 | GAAAAAAGAAAAAAA[A/G]AAAGAAATTTAAAAA | 23603 |
rs532278650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725033 | AAAAAATCCATCTTT[C/T]GCCAGGAACTTTCCT | 23603 |
rs532306211 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711023 | TCAACCTCTAGGAGA[A/G]TGTAAAGGCATGCTT | 23603 |
rs532338981 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707796 | CAATAATAAAAACAT[A/T]GTCCAATTTAAAAAT | 23603 |
rs532341883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693731 | GTCTGAAGGAGGAAT[A/G]TGCCTACCACCTACT | 23603 |
rs532382274 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108700214 | TCATACGACCCAACA[G/T]CTGCATCCTCACCAG | 23603 |
rs532422321 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732866 | GCAGCCATGATCGTG[G/T]CATTACTTTTTGCCA | 23603 |
rs532459611 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732063 | AGAAGCCCCGCCCAA[A/G]GACCGCAACCCTATT | 23603 |
rs532469870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108655570 | TTTTTTTGGTGGAGA[C/T]GGGGTTTCGCTGTGT | 23603 |
rs532500369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648303 | AAGACAGGAAAAACC[C/G]AAGAGGCTCCTGTTC | 23603 |
rs532530729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709034 | TGCTTGGATTATAGG[C/T]ATTAGCCACCATGCC | 23603 |
rs532548430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108668992 | AAGCTAGGAGTGAAG[C/T]GTAGTTTCTGGGAGT | 23603 |
rs532566002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708365 | AAAAACATTATAAAT[G/T]AAAGAAACCAGTCAC | 23603 |
rs532707711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660938 | AGTCATAAACATTGT[G/T]TATTCCCAGTTAAAA | 23603 |
rs532795438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691298 | CCCACCCCTAATGGG[C/T]GAAGATATTCAACTT | 23603 |
rs532860459 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730519 | ATTCCCACCCTCCAC[G/T]TCTGACCTCATCCTC | 23603 |
rs532939411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706487 | AAAGAAAGAAGTAAA[A/G]CTATTTCTGTGTGCT | 23603 |
rs532971688 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646150 | CAATACTCATTCAAT[C/T]GCACCCTCTGGCCTT | 23603 |
rs532977356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108714172 | GAGGTGGGCGGATCA[C/T]GAAGTCAAGGGATTG | 23603 |
rs533057193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108729938 | AGGACAATGAGATGC[A/G]TTATTATATAGAGTG | 23603 |
rs533087703 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108684507 | TAGTGGCAAAAGCAG[A/C]AGCAATTTCACTGTC | 23603 |
rs533087966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676590 | CAGCCTGGCCAACAT[G/T]ATGAAACTCCGTTTC | 23603 |
rs533119067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698436 | TTTTTGAGACGGAGT[C/T]TCACTCTGTCGTCCA | 23603 |
rs533122437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660052 | GGATGAAGCAAAATA[C/T]GGGAAGGACATCCTA | 23603 |
rs533125274 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661967 | AAACACATTTGCTTC[C/G]CCCCACTCAGAGAGC | 23603 |
rs533129901 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720673 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 23603 |
rs533130561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697878 | CAATCAAATATCAAC[C/T]GTAAAATGTATAACC | 23603 |
rs533146756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675490 | CAAAATGAAAGGAAC[A/G]GGGAAAAAAAAACCC | 23603 |
rs533168629 | in-del | -/ATTT | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658187 | CTTTTCGCCCTGCGC[-/ATTT]ATTTATTTATTTATT | 23603 |
rs533169375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720735 | TCACCATGTTAGCCA[C/G]GATGGTCTCGACATC | 23603 |
rs533184338 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690558 | TTGTAAAACTACAAA[C/G]ATTTTATTATCAGAA | 23603 |
rs533284452 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716775 | CCCCAGTAAAACAGA[C/T]ACAACTCACTGCAAA | 23603 |
rs533314997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689518 | GACTGCTTTCTACAC[A/G]GTTTCCCTTATCTAA | 23603 |
rs533333637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666684 | GCCTGGGTGTCAGAA[G/T]ACACAGGCTCCTGTC | 23603 |
rs533351179 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108688985 | GCAGTGAGCTGAGAG[C/T]GTACCACTACACTCC | 23603 |
rs533365935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696704 | TGCTATTATTCATCC[A/T]CTGAAGGACTAAAGA | 23603 |
rs533397731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720123 | CCTGGGAGGGCGACG[C/T]TGCATTGAGCCTCAA | 23603 |
rs533423115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108721759 | AAGTTTATAAAAGAA[C/T]AGAAAAATAGACAGG | 23603 |
rs533464598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659404 | TTTCCCCTGCTATAC[A/G]ATTAGTACATGTATA | 23603 |
rs533473559 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108681749 | ATATTAATTTTGAAG[A/T]ATTAAGTTTAAGGAC | 23603 |
rs533550226 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695522 | TAATAATGTGATAAC[A/G]CAGGCTGTGGTACCA | 23603 |
rs533659296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714316 | ATTGCTTGAACCCGG[A/G]AGGCAGATGTTGCAG | 23603 |
rs533681797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660391 | AGGAGGCGGAGGTTG[A/C]GGTGAGCTGAGATCA | 23603 |
rs533744106 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715588 | GCATTGCTGAAGAAA[A/C]GTCCCTTGGGAAGAC | 23603 |
rs533778247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676665 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 23603 |
rs533850902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108729227 | TTAAACATAAAACTT[A/T]TATCAAAAAATCCAA | 23603 |
rs533858044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714908 | TGGTTGGGGACCACC[C/T]AAAGTCAAACCTAAG | 23603 |
rs533903727 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108669062 | TTTCACAAAGTAGTA[C/T]ATGAAAGGTAAACTG | 23603 |
rs533932048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108697136 | ATGAGGTTGCAATAA[A/G]AAGCCTTATTTACTG | 23603 |
rs533938295 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694176 | AGTCCCAGCTACTCA[C/T]GAGGCTGAGGCAGGA | 23603 |
rs533973996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691458 | GGAGATACAGCAGCT[C/T]TCCCAGACTGGGGTT | 23603 |
rs534048331 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666394 | ACTGGTAAAGAGGGG[G/T]TGGTGTTCTCTACGG | 23603 |
rs534120350 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656874 | TTAAGAGTCATCACC[A/G]CTCCCTAATCTCAAG | 23603 |
rs534128203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675993 | GGTCAAAGGTCAGGG[C/G]TTCCGAATAGATAAA | 23603 |
rs534130182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108682007 | ATATCCAAATGCAGA[A/G]TAAATACTAAAAGGA | 23603 |
rs534186580 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655268 | TTTAGACAACTGATC[A/G]TATTATTTATGAAAT | 23603 |
rs534199840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712698 | ATTAAATATAAAAAT[C/T]TGGCCGGGCACGTTG | 23603 |
rs534217868 | snp | C/T | 3.29614e-05 | 0.00405951 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658753 | AGCAACAATCTCTTG[C/T]TTCCTGGGATCAATG | 23603 |
rs534235919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713520 | TAACTCAATATCATT[C/T]AGTTTTTAAAGTTTC | 23603 |
rs534289218 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708703 | CTGACCTCAGGTGAT[C/T]TGCCCACCTTGGCCT | 23603 |
rs534371951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108666017 | AACCAATGCTATGCT[G/T]GCATAAGCCGACCGC | 23603 |
rs534418291 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693710 | ACCTAAACTAGACAT[C/T]CTGGAGTCTGAAGGA | 23603 |
rs534602808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108650532 | TGGTTAGTATAGCCA[A/G]TAAAAAGACTGACTT | 23603 |
rs534611446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649532 | CTAGCAAACCACATC[A/G]TACATGACACTCAAG | 23603 |
rs534714196 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728842 | GACATACAAGTGTCA[A/G]AAAAGAGTTTTCATA | 23603 |
rs534810330 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703426 | AAAGCAGGTAAAAAC[A/G]TGAAAGGACAAGAGG | 23603 |
rs534850110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711110 | GTTCATAGTTGTACT[C/G]CCAGCATTCTGGGAG | 23603 |
rs534861908 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660190 | GGCACGGTGGCTCAC[G/T]CCTGTAATCCCAGCA | 23603 |
rs534961729 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733318 | CTGAGACTACAGGCA[C/T]GCGCCACCATGCCCA | 23603 |
rs535022900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679503 | TCCTTTTTAAAATAG[C/T]TTAATGCCAGTCCAC | 23603 |
rs535048856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687797 | CAATAATAATAATAA[A/C]AATTTAATTAAAATT | 23603 |
rs535091480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682226 | AAGCACAAAGATGGT[A/G]GAAATAAAACCAACT | 23603 |
rs535149157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663376 | ATGCAAAAACTTGTA[A/C]AAGAATGTTCATAGA | 23603 |
rs535151852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672946 | CTCTTCCTGTATTCC[C/T]GTCTCTTCCTCTCCT | 23603 |
rs535245759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108675119 | GCAGCCATCAACACT[A/G]AGGGGAAACCCTCCA | 23603 |
rs535321973 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704426 | TCAGTGAGCCAAGAT[C/T]GCACCACTGCACTCC | 23603 |
rs535399930 | snp | G/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732759 | AAGACAGCTATCACA[G/T]CAAATTATTTATCCT | 23603 |
rs535412454 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CORO1C | GRCh38.p7 | 12:108714309 | CAGGAGAATTGCTTG[A/T]ACCCGGGAGGCAGAT | 23603 |
rs535462555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689840 | TGGCTTTGGGTGATA[C/G]ATACTGAGAATTCTT | 23603 |
rs535500576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718364 | CAAGAGTGAGACTCC[A/G]TCTCGAAAAAAAAAA | 23603 |
rs535556794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657933 | GGGCAAGTCCCCAGG[C/G]CTCAGTAAGCACCAG | 23603 |
rs535559139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108719421 | ACCAAAGTCTACAGT[C/T]TTTCAGACTTTAGTA | 23603 |
rs535563814 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726202 | GCGGGCGGATTATGA[A/G]GTCAGGAGATCGAGA | 23603 |
rs535570245 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691324 | AACTTGGCAGGAGCA[C/G]ATGATTTGCTACATG | 23603 |
rs535639813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696423 | GGGGAGGGAGGGGAC[A/G]GGGGGGTTGTATGTG | 23603 |
rs535653863 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108688543 | CTTCATGTAAGAATG[A/T]TTCCTCACATAATTA | 23603 |
rs535658945 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688920 | CTGTAATCCCGGCTA[C/T]TCGGGAGGGCTGAGG | 23603 |
rs535703871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696856 | GGACTGAGGACTTTC[C/T]ATATTCCTCCGGCAG | 23603 |
rs535764331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108726124 | AGGTGTGAGCCACCA[C/T]GCCCGGCATGAAATA | 23603 |
rs535821140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664149 | AATCATTATCTTCTA[C/T]ATGAAGATTAAAACA | 23603 |
rs535840869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108656401 | GGGGCAGCCCCCGCC[C/G]GGCCAGCAGCCCCAT | 23603 |
rs535901413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694334 | CAGGTCGCTGCACAT[A/G]CAGGCACTAAGGAAT | 23603 |
rs535902030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710377 | CTTTCTTAATAAACT[C/T]GTTTTCACTTTAAAA | 23603 |
rs535921655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649750 | TTTTCTTTTTCAGTC[A/G]AGACGGGAAACAACA | 23603 |
rs535970064 | snp | A/C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648614 | CCTCACCACACTGGC[A/C/T]GTGTCTGTGGTTTTC | 23603 |
rs535985851 | snp | C/G | 1.6557e-05 | 0.00287719 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657313 | GCGTACCGGATTCCA[C/G]AGAGCCAGCTGCCGC | 23603 |
rs535986948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665518 | GCAGAGACTTCTATC[A/G]GACTGAAAATCAAAG | 23603 |
rs536002785 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694128 | CTCTACTAAAAATAT[A/G]AAAATTAGCCGGGCA | 23603 |
rs536008885 | snp | C/T | 0.000198255 | 0.00995431 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662057 | CACATTGCGGGCCGT[C/T]GGATGCCAAGCCACG | 23603 |
rs536038958 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108675324 | TCACATAGCAAGGAA[-/T]CTATCTATCAAAGAC | 23603 |
rs536050844 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108670231 | CATGTGATCAGCCTC[A/C/G]GGTGTGTGTGGGAAG | 23603 |
rs536052330 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657619 | GGTCAAGGTCCCTCT[A/G]TGAGGCTGCAAGAAT | 23603 |
rs536067440 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108678556 | TTCTAGAAAAAGCCA[A/C]TACCAAGGACATGCG | 23603 |
rs536070842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687841 | AGAAGAAATGATATT[A/G]CTTAGCTGTAAGGGC | 23603 |
rs536102504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108715923 | TGGATCACAAGGTCA[A/G]GAAATGAGACCATCC | 23603 |
rs536195768 | in-del | -/GA | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108711808 | ACACTCAAAACACCT[-/GA]GTAAATGTTACATTT | 23603 |
rs536212579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648001 | GTGTGTCCACTCCTT[C/T]TCTCTTACCCAGGAC | 23603 |
rs536270024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685272 | ATTCCCAGCTCAGCC[A/C]CAATAAATCCACAGC | 23603 |
rs536384601 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647318 | CAGTGCCTCCCTTTC[C/T]GCCCTCCCTAGGACC | 23603 |
rs536410150 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108725158 | GCAAAAACACTGGAG[-/GT]GTTTTTAAGACCGCC | 23603 |
rs536454024 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713487 | ATACCAGTAAAAATG[A/C]ATTTTGTTTCAATTC | 23603 |
rs536528239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655948 | AGGAGCGTCTCTGCC[C/T]GGCCGCCCATCGTCT | 23603 |
rs536541847 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647197 | GATAAAAAGCTCAGC[C/T]TTTAAATCACGTTTT | 23603 |
rs536556453 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646596 | TATAATCATCTGAAG[C/T]ACAGGATAACCGAGA | 23603 |
rs536556891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716684 | TATAAAATGGAAGAA[A/C]TAAAATAAATGATTT | 23603 |
rs536609027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649413 | ATTGTATCTACAACG[C/T]GGGTACAAGGTCTTC | 23603 |
rs536631941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686168 | TAAGAACACAATTCT[C/T]ATTCGTCTGCACGAC | 23603 |
rs536664175 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703225 | AAAAGTAAGCTAATG[C/T]AGAAGAAAAAAGGAT | 23603 |
rs536722779 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732181 | CCCGAGGCTCCGCCC[C/T]GGCTCCGTCACACCC | 23603 |
rs536724663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724174 | CAACAACAACATAGG[G/T]ACATGCTACCAACTG | 23603 |
rs536741675 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723866 | TTTCTGGCAAGATGC[A/G]ATGCAAGGGCACCTT | 23603 |
rs536797731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678191 | AAGCCTCTATACATA[C/T]ACACACACCCACACA | 23603 |
rs536801224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108656055 | TGGGAGGTTAGGAGC[A/G]TCTCTGCCTGGCCGA | 23603 |
rs536802512 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671511 | AAAAAAAAAAAGACT[A/G]GAAACTATATATTGA | 23603 |
rs536817663 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696765 | AAGTCATGGCAGAGT[A/G]GCAAGCCACAGCTTG | 23603 |
rs536836878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699555 | AACAAGCTATGGCTG[C/T]CTTCTCAGTTGGCTG | 23603 |
rs536860511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662694 | AGACACTTAGCTAAG[A/T]CTGTGGTTCTTGATG | 23603 |
rs536892067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722263 | ACCCTGAATAACAGC[A/G]GTAGTCTAGCAGGGA | 23603 |
rs536908279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692639 | ATCACTGTCACTGTG[C/T]CCTCACAAGGCATGG | 23603 |
rs536988168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108656456 | CTCCACCCGGCCACC[A/G]CCCCATCCGGGAGGT | 23603 |
rs537183306 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108672390 | TTAGTTTTTCAACTA[A/G]AAGTCGTTTAGTTTT | 23603 |
rs537234109 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108710450 | ACTGTCATAATAAAT[G/T]TTTAATAAGGAGATA | 23603 |
rs537297510 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668505 | GTCTTTGTCAAATGC[C/T]TTCCCACCCGCCAAA | 23603 |
rs537326835 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648752 | CTTCAAGGAGATGAG[A/G]ATTGGGTCTGCATTC | 23603 |
rs537334730 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718146 | ATCACAAGGTCAGGA[C/G]ATTGAGACCACCCTG | 23603 |
rs537341312 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691157 | TCCACACAAGCAAGA[A/G]GACTGCAGTATAGAC | 23603 |
rs537405765 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656911 | GGGACACAAACACTG[C/T]GGAAGGCCGCAGGGT | 23603 |
rs537436478 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108707852 | TTTCCAAAGAAGATG[C/T]ACAAATGTCCAATAC | 23603 |
rs537439056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678756 | TAAACCTTGGTATTA[C/T]TCAAAATGTTAATAC | 23603 |
rs537478816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714999 | ATGAAAATGACTGCC[A/G]AAAATCAAGTCTGAC | 23603 |
rs537498374 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732266 | TTGTCACATTCCTAG[A/T]GCAGAGTGGCCGCCC | 23603 |
rs537509410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108716810 | ATTACTTACTAACAT[C/T]CACAGGGTTATACGT | 23603 |
rs537522284 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646673 | AAGGAAAAGAAGAAA[C/T]ACGACGTGAGCTTTT | 23603 |
rs537529999 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108729920 | AGAACGTTCTGCCAG[A/G]TAAGGACAATGAGAT | 23603 |
rs537561701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725381 | GAACAGGAATGTATT[C/G]AGTACCTACTCTGTA | 23603 |
rs537600133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671281 | GTCAAGGCATGATCG[C/T]GCCACTGTACTCCAG | 23603 |
rs537616444 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647264 | TGGAATGTGGCCTAT[C/T]GCTGGTTGACAAATC | 23603 |
rs537622279 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655004 | GCCACTGCGCCTACC[C/T]TATTTTATTTTTTTA | 23603 |
rs537635752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684950 | GTCTTTGCATTCCTA[C/G]GCTCTGCCCAGGAAA | 23603 |
rs537696176 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108730122 | CAAATGTCTTATAGG[A/G]GGGAAAAGCCTTTGT | 23603 |
rs537782911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693834 | TTCATCTTTAGCTCC[A/T]ACGCAGAGGAAAAAA | 23603 |
rs537820076 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676046 | AAGGAGGAATCTTTA[A/G]ATTAAGACTTAAAAG | 23603 |
rs537918688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654997 | AGGAATGGCCACTGC[A/G]CCTACCCTATTTTAT | 23603 |
rs537974302 | snp | A/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108661794 | CTGAAATTATAGCAG[A/G]AAATTCATAGCTTTC | 23603 |
rs537980011 | snp | A/T | 0.000205461 | 0.0101335 | intron-variant | CORO1C | GRCh38.p7 | 12:108654460 | ATGTATACATTTTTT[A/T]AAAAATAAATTTTTA | 23603 |
rs538021318 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658999 | CTACAGATACAGTGA[G/T]AATACACATATGTAT | 23603 |
rs538071752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662768 | TGGAAAACAAAAATA[C/T]ACTTAATATTTTTAT | 23603 |
rs538151153 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730785 | TTACTCCAGCTCCAG[C/T]TCTGCCCCGCCCCGC | 23603 |
rs538159863 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108688688 | GAGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 23603 |
rs538181579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659762 | GGTACAACAGTGGAA[C/G]GGAAAAGCCAAGAGT | 23603 |
rs538188466 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677447 | TCTTTATGAAAAGGA[A/C]TTTCTTAACCAGGGT | 23603 |
rs538204647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653245 | CCCAAAAGAATTTTC[C/T]ATCTCATGTTACTAA | 23603 |
rs538208987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662452 | GTTGAAGCAATTCTC[C/G]TGCCTCAGACTCCCA | 23603 |
rs538211496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708450 | CAGAAAGTAGATTCA[C/T]GGTTGCTTAGAGTTT | 23603 |
rs538236850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700681 | ATTAAGAAAAGAAAA[A/C]GGGCTCATCCTTATG | 23603 |
rs538241897 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679035 | AGTATCGCTTGAACC[C/T]GGTAGGCAGAGGTTG | 23603 |
rs538273561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708648 | TGTATTTTTAGTAGA[C/G]ACAGGGTTTCACCAT | 23603 |
rs538308751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693391 | TTTCCATCAACGTGA[C/G]AGAAGTCACTGCTTT | 23603 |
rs538331436 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657676 | TCTCTCCACCATATC[C/T]TGCTGCCAACCCAAG | 23603 |
rs538340244 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645831 | ATGGCACTACACATT[C/T]CACGTTCAATCACAG | 23603 |
rs538421844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108669381 | GCTAGGAATCCACTA[C/T]AGGTATCCATCAAAA | 23603 |
rs538430051 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678652 | GCAAAAGAGAATATG[A/G]AAGTCTTTTTGCCAA | 23603 |
rs538447191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108686012 | CAAATCAGCATACGT[C/T]ATTAAAAATACAAAG | 23603 |
rs538457723 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650925 | CTTCATTATTCCAAC[C/T]AAAAAAAAAAAATCA | 23603 |
rs538463684 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108711759 | AAATGCAGACAAGAC[-/AG]GGTATTTATATTGCA | 23603 |
rs538464081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712720 | GGCACGTTGGCTCAC[A/G]CCTGCAATCTCAGCA | 23603 |
rs538588392 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657717 | GTGAAAATAAAACAC[A/G]TGAAAGGACTCTGAC | 23603 |
rs538610348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655119 | CCTACAGCCCAGTGG[A/G]TGACAGAAGCTATTA | 23603 |
rs538612039 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722648 | GATAGAAATTACTAC[C/T]AGTAGATCTGAGTTC | 23603 |
rs538613625 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702034 | CTAAAGCAGCCTAAC[A/G]GGTAAGAGCCAGGTC | 23603 |
rs538627705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684365 | TTACAATTCCTTTCA[A/G]GAGCAATTTGGTAAC | 23603 |
rs538734067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647771 | TGCCACTTCTGATCC[C/T]GAAGCCTGTGCATTT | 23603 |
rs538749211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655838 | ATCTCTGCCTGGCCG[C/T]CCATCGTCTGGGATG | 23603 |
rs538749216 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647285 | TTGACAAATCTGAAA[C/T]GGAATGTCTCCAAAT | 23603 |
rs538801605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108706648 | CACCCAGGGTGGAGC[A/G]CAGTGGTGCAATCTT | 23603 |
rs538820581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652664 | CTGGCTCCTGGCTCT[A/G]ATTTTACTCCCCTGA | 23603 |
rs538914205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698702 | ATGGGCCACTGTGCC[C/T]GGCCAGAAAATAACT | 23603 |
rs538958269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653331 | AAGGTAAATGCACTT[A/G]ACACCTGTTAACATC | 23603 |
rs538960729 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675489 | TCAAAATGAAAGGAA[C/T]GGGGAAAAAAAAACC | 23603 |
rs538999582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692355 | CCAAATGTCCACATC[C/T]GTACAAAGGGCTACC | 23603 |
rs539026818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675856 | GCCAAAAGGACAGAA[C/T]CTGAATCTGACCGCA | 23603 |
rs539111699 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730845 | AGAGCTGGTCTCGCA[A/C]CCAAAGCCAGGAAAC | 23603 |
rs539157894 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733375 | AGATGAAGTCCTGCT[A/G]TGTTGCCCAGGCTGG | 23603 |
rs539187063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667735 | AGTTCCAAGGGCTCC[C/T]ACATGAAAAAGTGAA | 23603 |
rs539260918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706264 | AACACTCAAGAAACT[A/G]GGAATAGAAGGGAAT | 23603 |
rs539262977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714277 | AACTGTAGTCCCAGC[G/T]ACTCGGGAGGCTGAG | 23603 |
rs539274164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696982 | TGTGCTGCTTGCTGC[A/G]TATGTGTGTGTCTTT | 23603 |
rs539377717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689667 | CCCCATCCTGGGGAA[A/G]GCAAACAAAGATACT | 23603 |
rs539395436 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722054 | GCCTCCTTACGTGGG[A/G]TCTGCCTGACTTCAC | 23603 |
rs539441363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683118 | AGTACATCCAAAGAA[C/T]GTAAAATTATTAGAA | 23603 |
rs539475117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712148 | ACTGTTACCTGTATG[A/G]CAGGTACTTTAATGT | 23603 |
rs539484876 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697932 | ACCAAAATTATAAGG[A/T]AGACATCAAGAAGGC | 23603 |
rs539503129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705304 | GGCAACATGGTGAAA[C/T]CCAGTCTCTACTAAA | 23603 |
rs539504360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713893 | TGGCCAGTTTGTGTA[A/C]CACTTTAAATGTGAA | 23603 |
rs539508001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108668440 | TTCAGGGCAAAAACT[A/G]TATTAGAAAGCATTA | 23603 |
rs539569330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711675 | ACAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 23603 |
rs539580811 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686092 | AACCATACTAATAAC[A/G]GCCTTATATGGTAAA | 23603 |
rs539609145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680931 | ACTGGGATCACAGGC[A/G]TTCATCCTATTTTAC | 23603 |
rs539624673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689997 | GTGGGTTTTCCATTT[G/T]TTTCAACTTCCTTTT | 23603 |
rs539647316 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108680339 | AGGCCTAGGTTTCTT[A/C]ACATTCCTCCACTTT | 23603 |
rs539706317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108728373 | GTACTATACAATACT[A/G]CCACACATATAAACC | 23603 |
rs539754655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727370 | CTAGAAGTAGAAAGG[C/T]GATGAAGTAATAAAT | 23603 |
rs539754966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718657 | AATAGGAAAGTATAG[C/T]GCTTACAATCTTACT | 23603 |
rs539763747 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108690945 | GACATTGGAGATTGA[C/G/T]CTACTGAAACCCTCT | 23603 |
rs539800303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108652019 | AACAGAGCCAGACTC[C/T]GTCTCAAAAAAAAAA | 23603 |
rs539809878 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704534 | CTAAATACATGTGGA[C/T]AGAATGATATAGAAG | 23603 |
rs539855137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659211 | AACAATCAACCAAAC[A/G]AAAACAAAGAACCAC | 23603 |
rs539873779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696564 | TATTCATGCCAACGT[C/G]GTAGATTACACAGAG | 23603 |
rs539916574 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682532 | TAACCATATAATTTC[A/T]AAATAATTAAGGCAA | 23603 |
rs539917258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108651573 | GACTCTGGTTCTTCC[A/G]CTCATAGGGTAGGAA | 23603 |
rs539920496 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645398 | AACCACATGCCCTAC[A/G]GTGTTTCACCACCAT | 23603 |
rs539951115 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108650967 | TTGGTTTGTTTGTTT[C/T]TGTTTGTTTGAGACG | 23603 |
rs539964717 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681300 | AAATTAAAGAGATAA[C/T]GTCTGAGAATTTTTC | 23603 |
rs539982739 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108712470 | CCCAGCTACTCAGGA[-/G]GGCTGAGGCACGAGA | 23603 |
rs539986714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673177 | GCCAAGTTGTGAATG[C/T]AAAAGAAAAGTTCAG | 23603 |
rs539996139 | in-del | -/TA | 0.0115144 | 0.0749975 | intron-variant | CORO1C | GRCh38.p7 | 12:108709119 | TGCAGATTATTTGAT[-/TA]TATATATATATACTA | 23603 |
rs540072343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726806 | TGACTAAATCGTGTT[C/T]GCTGGCCATCTACCC | 23603 |
rs540173676 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720421 | GTTTCAATAAAGGAA[A/T]GTGTATGTATATCTG | 23603 |
rs540195421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659891 | TAGCTACATAGATTC[A/G]GAAACGGATTCTGAA | 23603 |
rs540205562 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108719372 | TTACAAAATAATTCA[-/T]TTTTTGTGACCACTT | 23603 |
rs540240140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108667927 | CTTGGGTTTCTCTCA[C/T]GTGCTAATTTTAAAG | 23603 |
rs540301202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698351 | TCACTTCATAGCTGA[A/G]AACCATGGAAGGTGA | 23603 |
rs540322805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727905 | ACCAATAAAAAGACA[A/G]CCCATTAAAAAACGG | 23603 |
rs540338245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706416 | TTCAGGATTGTAGTA[C/T]AGGTTCTAGCCAAGG | 23603 |
rs540367068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652769 | GAAAAACAAACAAAC[A/C]AACAAAGACTAAGAG | 23603 |
rs540412248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675244 | TCCCTTAAAATAAAC[C/T]AGGACTTCCGAAAGA | 23603 |
rs540428821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108657521 | CACCAACTGCCATTC[A/G]TGTTCACCTGGGTGT | 23603 |
rs540433184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706522 | ACATGATCTTATATA[C/T]AGAAAATCCCGAGGA | 23603 |
rs540476017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664373 | GTGTTTAGGGTTCAG[C/T]TCAGTTCTACTGTCC | 23603 |
rs540518680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108711361 | GGTATCAGAGCAAGA[A/C]CATGTCTCAAAACAC | 23603 |
rs540576826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667303 | AGGCCAATTACCACA[A/G]TAAGGACAGATCTGA | 23603 |
rs540605961 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | CORO1C | GRCh38.p7 | 12:108672657 | TGGTGTTTTTGTTTT[G/T]TTTTTTTTTTTAAAC | 23603 |
rs540607871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108680439 | TGAACACCATATCAT[A/G]TAGAATCTGGGTGTC | 23603 |
rs540645708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679793 | GCTCTACTGATTAAA[C/T]AGGTGACTTTAGACA | 23603 |
rs540683135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690059 | GTTTTGTTTGAATTT[A/C]TTAAGCCCCTGCTGC | 23603 |
rs540772739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673347 | CTCTTCAATTCCATG[A/G]AGGCTGACAGAGGTG | 23603 |
rs540789631 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674330 | AAGGCGGGCGGATCG[C/T]GAGATCAGGAGATGG | 23603 |
rs540866473 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108694878 | TTACTCATATATGAA[C/T]TGTGTGAACTAACAT | 23603 |
rs540885443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679188 | AAAAAAAAAAAAAAG[A/G]AAAGCTTTAGCTATC | 23603 |
rs540902103 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667780 | CCATTGTGGTTCTGG[-/A]AAAAAAACAACTTTA | 23603 |
rs540910200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108651038 | ATCTCGGCTCACTCC[A/G]CCTCCTGGGTTCAAG | 23603 |
rs540927564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688160 | AGGTGATCTGCCCAC[C/T]TCAGCCTCCCAAAGT | 23603 |
rs540931145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712189 | CGATGTGTTATTCAA[C/T]AGAAAAAGGCAGGTA | 23603 |
rs540951974 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720645 | TCCTGCCCTCAGCCT[-/C]CCTGAGTAGCTGGGA | 23603 |
rs540983600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655571 | TTTTTTGGTGGAGAC[A/G]GGGTTTCGCTGTGTT | 23603 |
rs541034144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662927 | CTTACAAATCATACA[C/T]TTGATAAGAGACCCA | 23603 |
rs541110298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648370 | ATCATGGTGGTCTGT[A/G]GCCACACTTGGCTCC | 23603 |
rs541115614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717042 | GTGCAAACATTAGCA[A/T]GCCGCTGTGGCAAGT | 23603 |
rs541143538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726838 | ACTGAGGAGACTGTG[A/C]GCCAGTCATTACTGT | 23603 |
rs541164367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663681 | TTAGTGTTGGGGAGA[A/G]TGGAGGGAGGCAGGT | 23603 |
rs541171484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647588 | CAACACTGTTCAAAA[C/T]TTGTAAGATATAAAA | 23603 |
rs541184165 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661532 | TGGGATTAAAAGTGA[-/T]TTTTTTTTTCCTTTT | 23603 |
rs541212312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108656257 | AGTGAGGAGCGTCTC[C/T]GCCCGGCAGCCACCC | 23603 |
rs541216383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687556 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 23603 |
rs541246505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669694 | AAAAAAAAAAAAGGC[A/G]GGGGGTGGCGGGGGG | 23603 |
rs541262131 | snp | C/T | 0.00119737 | 0.0244387 | splice-donor-variant, intron-variant | CORO1C | GRCh38.p7 | 12:108702795 | TGCCAGAGTCTCTTA[C/T]CCTTCCAACGCATGT | 23603 |
rs541281005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686537 | ACTACTTTTCTGGCA[C/T]GAAATTGAAGTAGTT | 23603 |
rs541299050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719229 | ACAAATAATTTTAAG[G/T]AGAAGGCCAGCAAAA | 23603 |
rs541323257 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686738 | GCCAGCACCAAGTTT[C/T]CCAAAGGCTCTGCTC | 23603 |
rs541341038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723271 | ACATTTGAGTTTTTA[A/T]GTTAATAAATCAGTC | 23603 |
rs541365265 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732867 | CAGCCATGATCGTGG[C/T]ATTACTTTTTGCCAT | 23603 |
rs541442801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671318 | TGACAGAGCAAGACC[C/T]TGTCTCAAAAAAAGA | 23603 |
rs541485307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673532 | GATGAAGGTGGCTAC[A/G]CTAAACAACACATTT | 23603 |
rs541485473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709044 | ATAGGCATTAGCCAC[A/C]ATGCCTGGTGTGTTT | 23603 |
rs541510121 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108702047 | ACGGGTAAGAGCCAG[G/T]TCTGGGAAAAGCAGA | 23603 |
rs541528145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712256 | TTATTTAAATGACAA[C/T]GCCAACAGTAAAAAA | 23603 |
rs541549186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700908 | AATTTTTTCATCCAT[A/G]GAGGGCATCCCCAGA | 23603 |
rs541585569 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660848 | TGATTATAAAAAACA[G/T]GGCATCTTTTTTGAA | 23603 |
rs541611409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108701594 | ATTTCAATGGAAAGA[C/T]TAAGGGAAAGAATTA | 23603 |
rs541618407 | snp | A/G/T | 1.66297e-05 | 0.0028835 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678279 | GAGCTTACCATGACC[A/G/T]TGCAGTCCTCTGAAC | 23603 |
rs541689033 | in-del | -/A | 0.0121321 | 0.0769341 | intron-variant | CORO1C | GRCh38.p7 | 12:108725825 | TTATTTATTTATTTT[-/A]TTTGAGACGGATTCT | 23603 |
rs541696310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716056 | GAATCGCTTGAACCC[A/G]GAAGTCGGAGGTTGC | 23603 |
rs541776595 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725309 | AATGTATTAAACTTA[C/T]TCTATTTGCTTCTCT | 23603 |
rs541811699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656650 | GAAATCAGATTGTTG[C/G]TGTGTCTGTGTAGAA | 23603 |
rs541835598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726150 | AAATATTTTTAATTA[A/C]AGTATTTTAAAAATA | 23603 |
rs541890995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108727621 | GCATACCTTAAAATA[C/T]ATTAATTCAAACCTT | 23603 |
rs541892862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108718963 | AATATCTCTAGGGAA[A/G]TGAAGACAAATAAAC | 23603 |
rs541933883 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690255 | AGGAGGCTTTACTTT[-/A]AAGGGAACCAGAAAT | 23603 |
rs541947854 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653578 | AATTGAGCCTACAAG[-/A]AAAAAAAAGGGAACT | 23603 |
rs541954139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719611 | AGGCCTGCCCTATGA[A/T]TTCTCTGGTGCTGGG | 23603 |
rs541966877 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | CORO1C | GRCh38.p7 | 12:108702845 | AATGCTGGGGGCATG[C/T]AGCCGGGCTGAAGTA | 23603 |
rs541999122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719607 | CCTAAGGCCTGCCCT[A/G]TGATTTCTCTGGTGC | 23603 |
rs541999195 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687555 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTTGA | 23603 |
rs542005129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679904 | ACCGTAAGGATTAAA[A/T]GAGAGAACACTTTTA | 23603 |
rs542026376 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656029 | CGCCTCTGCCCGGCC[A/G]GGACCCCGTCTGGGA | 23603 |
rs542044120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688737 | CACGGTGAAACTTCA[C/T]CTCTACTAAAAATAC | 23603 |
rs542047530 | snp | A/C/G | 0.00597534 | 0.0543715 | intron-variant | CORO1C | GRCh38.p7 | 12:108679036 | GTATCGCTTGAACCC[A/C/G]GTAGGCAGAGGTTGC | 23603 |
rs542061854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725638 | GAACGAGAACTACAG[A/G]AGGTACCCATAGCTC | 23603 |
rs542123000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717099 | ACTGAGTCAATAATC[A/G]GGGAACAGAAGCAGT | 23603 |
rs542134768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700682 | TTAAGAAAAGAAAAA[C/G]GGCTCATCCTTATGA | 23603 |
rs542158409 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648503 | CTGAAAACCCCTGAG[A/C]ACCCAGCTGGGACAG | 23603 |
rs542297651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724774 | TCCACATACAATGTA[C/T]AGGCCTTCCTACTCC | 23603 |
rs542300462 | in-del | -/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732105 | AAGCCCCGCCCACTA[-/C]CCCATCTCAACGTTT | 23603 |
rs542320949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687407 | TGGGAGGATCACCTG[A/C]GCCCAGGAGGTCAAG | 23603 |
rs542332518 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731735 | GTGCCCAAGCGCACG[A/C]CCCGCTCTCCAGTCA | 23603 |
rs542464777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670814 | ATAAAAACTACATTA[C/T]AGTGATTCAAAATAA | 23603 |
rs542483483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700794 | AAAAGCCAGTTTTTA[A/G]AACTGCACTCTAAAA | 23603 |
rs542485525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692977 | TAATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 23603 |
rs542522352 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108699848 | ATTTGAAAACACGTA[A/T]CAAATTTGTTCCCCA | 23603 |
rs542535359 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653778 | ACTGAACCCCAGGAA[A/C]AAGAACCCTCTGGAG | 23603 |
rs542539105 | snp | A/C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670475 | TCCAGGAAATGAAAT[A/C/T]GAATTTCAGCAGGAT | 23603 |
rs542566910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708758 | TGAGCCACCGTGCTC[A/G]GTCTATTTATTATTT | 23603 |
rs542591961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663010 | AATTGAAAAATAGGC[C/T]AGTCATCTAAATAGA | 23603 |
rs542594764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668874 | TATTATTTTCTTGGA[G/T]CTAATATTTCCCCCA | 23603 |
rs542597870 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108655369 | CCCCTTCCCCCTCCC[C/G]CTCCCCCTCTCCCTC | 23603 |
rs542607168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686697 | TTGGGATTACTAGCA[C/T]GTCAACCCAACAGGT | 23603 |
rs542759998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669461 | GACTCTCGATAGGCA[C/T]ATTATTATCATACCT | 23603 |
rs542782687 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646019 | ACGCAGCCTTGGTGA[A/G]AGATGGAGAGGCAGG | 23603 |
rs542850734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708187 | TACATGAGTCTTCAT[C/G]GAAGCATTATTTACA | 23603 |
rs542853011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108683791 | CCAAAAAACACTAGG[C/T]CCAGATGGTTTTACA | 23603 |
rs542883967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691144 | TGGCTGAGTCAGTTC[C/T]ACACAAGCAAGAGGA | 23603 |
rs542933572 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706945 | AAACAATTCCACTCA[C/T]AATACATCAGAAATA | 23603 |
rs542984606 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646837 | TTGATTGTTCTCAGA[C/T]GAATGTTTATACAAA | 23603 |
rs542998945 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731038 | CAGCCCTTCCCTCCC[A/C]GCACCTCGCCCAAGC | 23603 |
rs543089312 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108717166 | GAAGTCAACTGGGCA[A/C/G]TAAGAGAAGAAAAGT | 23603 |
rs543161127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723315 | CCTAAGAATGAAAGG[A/C]ATTAGAATCTTTAAC | 23603 |
rs543201534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693630 | TAATGTTAGTTCACA[C/G]TATGCATAAATGATT | 23603 |
rs543205412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691809 | GCTGGCCAAGGAAAC[A/G]CACAAAGGCTGCCTG | 23603 |
rs543269193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686868 | CCAAGCAACATGAGC[C/T]GAAAGGAAAATTCAG | 23603 |
rs543279911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698837 | CTCCACAGCTCATCA[A/G]TTCCCAGATTTGTGA | 23603 |
rs543308842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693964 | TGCACAAAGCACCCC[C/T]CTGGAGAGATCAAGC | 23603 |
rs543309721 | in-del | -/AGT | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108719208 | TCTATTCCTTATGAA[-/AGT]AGGACAAATAATTTT | 23603 |
rs543335242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730423 | AGCCTGCCACTTCCC[C/G]CAACACATTCAAATC | 23603 |
rs543380728 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664948 | TTTGCAAGATGCACT[A/G]TGACCCCACTTAGAA | 23603 |
rs543535814 | snp | C/T | 1.64963e-05 | 0.00287192 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662105 | GTGGCCTTCCAAAAT[C/T]ACCACAGGTTCAGTC | 23603 |
rs543558859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654806 | CTCCCAAGTTCAAGC[A/G]ATTTTCCTGCCTCAG | 23603 |
rs543626671 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675065 | ATTGTCGTGGTCTCA[C/T]CCAGCCCAACCTTCA | 23603 |
rs543628425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700889 | CTCACAACATCGTTA[C/T]AATAATTTTTTCATC | 23603 |
rs543629019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677068 | AAGCTTTCCAAACAA[C/T]GTTTCAGTCCACAGC | 23603 |
rs543877569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715345 | TGTAACTCACTTAAA[A/C]TATAATAGAAATGAC | 23603 |
rs543897043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698422 | ATAACTTTTTTTTCT[C/T]TTTGAGACGGAGTCT | 23603 |
rs543936628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108716003 | AGGCGTGGTGGCACG[C/T]GCCTGTAATCCCAGC | 23603 |
rs544008458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685398 | TAACAATGGCTAACA[C/T]TTTTTAAGTACTTAA | 23603 |
rs544048140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692711 | CTGACAGAATGAAAG[C/T]CCTGTCAAGTTACTG | 23603 |
rs544068026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108714468 | AACACACACACACAC[C/T]CCAAGGATAGTATCT | 23603 |
rs544092365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660697 | TCTGTTGCTGCTGCC[C/T]TGTATTGAGCCTTGA | 23603 |
rs544094286 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721163 | CTAACACTAGTGACA[C/T]CCACAAATTACACTT | 23603 |
rs544114556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723525 | TTCCCATGTGTGTCT[A/G]CTATGGTCTCTCATG | 23603 |
rs544134919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108677853 | GTGAAACCTCGTCTC[C/T]ATTAAAAATACAAAA | 23603 |
rs544146425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653654 | TCTAGGTATGCTGAG[C/T]TCATAAGGCAGGAGG | 23603 |
rs544189214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698897 | AGCTAAATACACACA[C/T]TTTAATACACAAAAA | 23603 |
rs544215078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690272 | AGGGAACCAGAAATA[C/T]CATCCTTGAGGTAAA | 23603 |
rs544223921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706948 | CAATTCCACTCACAA[C/T]ACATCAGAAATAAAA | 23603 |
rs544258658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682513 | CTATAAACTGTAATT[C/T]ATCTAACCATATAAT | 23603 |
rs544373723 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671272 | GCCCAGGAGGTCAAG[G/T]CATGATCGTGCCACT | 23603 |
rs544401973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728619 | CAATGAAGCTGTTAT[A/G]AAACAAAAAAAGTTC | 23603 |
rs544417126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658218 | TATTTATTTATTTTT[G/T]TATTTTTAGTAGAGA | 23603 |
rs544418405 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108675350 | AAGACTCAAAGACTA[C/T]GATGGTCATTTCAAA | 23603 |
rs544433001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651205 | GTAAGTATCAATTCT[C/T]TAATTGTGAGACCAG | 23603 |
rs544457278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689418 | CCCCTTTAAGAAGCT[C/T]AAGGTATCCCACACA | 23603 |
rs544457392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697264 | TACATATTCAGTATT[A/T]TTATGTACAGAGTCC | 23603 |
rs544510637 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704859 | TATTTACTTCCTGGC[A/C/T]GTGGTACAGTACAGC | 23603 |
rs544562491 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645016 | GAGGAGTATGGCACC[A/G]TGCTCGTCCACCAAA | 23603 |
rs544567086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659980 | AAGGGTCTGCCCCAC[A/G]CCTCCAGGCCCCTTT | 23603 |
rs544654248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683463 | GTCAGTGGAAAAAAA[A/C]TAAATAACAAAATCA | 23603 |
rs544693156 | in-del | -/TTA | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108725822 | TATTTATTTATTTAT[-/TTA]TTTTTTGAGACGGAT | 23603 |
rs544709982 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702588 | GCCTGGATAAAAATC[G/T]AAGTGGAAATGGAAC | 23603 |
rs544723830 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673834 | GTATACATATGTAAC[G/T]AACCTGCACATTGTG | 23603 |
rs544878022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708115 | CATAAGACCCAGCAA[C/T]CCACTCCTAGGTATA | 23603 |
rs544914327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108707161 | AGACTCCCAGAAGAA[C/T]TCTTTGTAGAAATGG | 23603 |
rs544930173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651764 | ATGGGCAGGAAATGA[A/G]GTATTAATTCCACAG | 23603 |
rs544970543 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108673425 | AGGTTAACGAAAGAC[A/G/T]CCATCTCCATTATAT | 23603 |
rs544982193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676264 | AAAGTTCTACTTTTT[A/G]ACATGGAAGGTGGTT | 23603 |
rs544990873 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646712 | AAGACTCCATGAAAT[A/G]AGAGCGGTGGTAATA | 23603 |
rs545025300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108729403 | GGTATGTATCTATTA[A/C]AATTCATCAGGCTTT | 23603 |
rs545084819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108714186 | ACGAAGTCAAGGGAT[C/T]GAAACCATCCTGGCC | 23603 |
rs545088515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108714837 | TCAAAGAAGAGCACT[C/T]GTATATTTACATTTT | 23603 |
rs545152018 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650665 | CACATATGATTGTTA[C/T]GAAAAGAAAGAGGTA | 23603 |
rs545155876 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694637 | AATGACTATGATCTT[A/G]TAACACATTTTTTAG | 23603 |
rs545184560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108721797 | CCCAGCTCTGGCCAT[C/T]ATAAGATGCCCCAAT | 23603 |
rs545191200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668728 | TGGAAGGAACAATTA[C/T]GCAATCCCATTGTCC | 23603 |
rs545250923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682557 | AGGCAAACGTTGACA[C/G]AACTTGAAGAAAATG | 23603 |
rs545261904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690581 | TATCAGAAAGCAAAA[A/G]CACGGAAAAGTTAAC | 23603 |
rs545306596 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646162 | AATCGCACCCTCTGG[C/T]CTTGTCTTAGCTTAA | 23603 |
rs545308282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654532 | TTTTCCTAGAATAAC[A/G]GAAGTTTGAACTATG | 23603 |
rs545321732 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728227 | AGAAATGAAAACGTA[C/T]GTTCACAGCATTATT | 23603 |
rs545344656 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671020 | ATAATAATAAAGTCT[-/A]AAAAAAAAAGAATAA | 23603 |
rs545368297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108653807 | AGAGTCTCTGAGGCC[C/T]TCAAAAGTTTGCATC | 23603 |
rs545477213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651960 | AACCAGGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 23603 |
rs545485762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666316 | CAAGGACTGCAATGC[A/G]AGAAGAAAGTGAGTG | 23603 |
rs545497373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730276 | AATATAGGATGTGTT[G/T]CTAAATCGTGATGCA | 23603 |
rs545503635 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697971 | CCATAGAGAAATGTA[A/G]GTTTTCTGATAACAT | 23603 |
rs545521139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659016 | ATACACATATGTATA[G/T]GCAGAGAGAGAGAGA | 23603 |
rs545610303 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686957 | TGGCTGGCCAGAGCT[A/G]AGGGTGATGTCTTAT | 23603 |
rs545693746 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645388 | CTTCTCTTTGAACCA[C/G]ATGCCCTACGGTGTT | 23603 |
rs545748816 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108667092 | AAAAAAAAAAAAGAG[C/G]CTACCATATTTTCAT | 23603 |
rs545753831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108719860 | AAAGCATGCTTCCAT[C/T]GGGATGTTACTTCAT | 23603 |
rs545821090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674406 | ACAAAAAATTAGCCG[A/G]GCATGGTGGCACATG | 23603 |
rs545857819 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700650 | TTCCATTTCCAACTC[-/A]AAAAAAAAAAAGGAA | 23603 |
rs545878584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705735 | ACAATACCAGCAAAC[A/G]AAATCAAGCAACACA | 23603 |
rs545884989 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704482 | ATCTCAAAAAAAAAA[A/G]AAAGTTATTTCCATA | 23603 |
rs545915706 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704958 | AGTGATCATTAAATG[A/G]TCAATTGGTGATGGG | 23603 |
rs545923777 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108725997 | GCGTGCCACCACACC[A/C]GGCTAATTTTTGTAT | 23603 |
rs545934999 | snp | C/G | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108727005 | TGTTATTTTAACATA[C/G]GCAATAAAGACATTC | 23603 |
rs546001394 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108681428 | TGCAATTTAGAACAC[C/G]TAAAACAAAGAGAAG | 23603 |
rs546034004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689279 | CATTATGTTAAAGTC[A/G]CACAACGCTTTACCC | 23603 |
rs546039780 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108679864 | GTAAAATAGTTAACA[A/G]TGATACTTATTAACT | 23603 |
rs546053562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711271 | GCTACTCGGGGAGCT[A/G]AGGTGGGAGGACTGC | 23603 |
rs546088480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710698 | CCTCCCGAGTAGCTG[C/G]GACAACAGGTGTGTG | 23603 |
rs546150246 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654445 | AATACATATATGTGT[A/T]TGTATACATTTTTTT | 23603 |
rs546173690 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | CORO1C | GRCh38.p7 | 12:108673016 | TAGGCCAATTAATAA[C/T]CCTAAATGACCTTTA | 23603 |
rs546194483 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108649837 | GATCACCAGATCAAA[C/T]GGCTGGTGTGCAAGG | 23603 |
rs546276080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688810 | GGAAACCAAGGCAGG[A/C]AGATAGGTCAGGAGT | 23603 |
rs546314549 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650778 | GTGTTTATAGTCTGT[C/T]GAACTTTTAGATGAC | 23603 |
rs546378368 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649288 | TGATGACAAATGCCA[A/G]TTATCTGGGGGACAG | 23603 |
rs546387420 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681418 | CATATCCTAGTGCAA[C/T]TTAGAACACCTAAAA | 23603 |
rs546434329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711832 | TTACATTTTCTCTAT[C/T]CTACTTCCATCTCAT | 23603 |
rs546435103 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675381 | AGGACTCAGAAATCT[C/T]GAAGAGGTTTCAATG | 23603 |
rs546443334 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729130 | AAGAATTGATATTCA[C/T]CCTTTTGAACATTCC | 23603 |
rs546469097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657848 | GCTTTCCTTGACCTC[A/C]GTAGTTTAATGAATG | 23603 |
rs546519191 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108650582 | ACTACCAAAACCCAC[A/G]AGAGTGTGACAACCT | 23603 |
rs546547419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726505 | CACCCCAAGAGAGGA[A/G]AGCATGAACAAAAGA | 23603 |
rs546568498 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108656858 | GAAGGCAGCATGCTC[A/G]TTAAGAGTCATCACC | 23603 |
rs546645148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108690710 | GCTTTCTGCTCATTA[C/T]TGCAGACAAGTAATT | 23603 |
rs546649367 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657086 | AAAATAAAAAATATA[C/T]AGTCAACAGCCTCTT | 23603 |
rs546711943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728176 | TATAGAGTTACCATA[A/C]AACCCATCGATTACA | 23603 |
rs546781559 | in-del | -/C | 0.00119784 | 0.0244435 | intron-variant | CORO1C | GRCh38.p7 | 12:108710326 | GAGGATTACGGGCTG[-/C]TCTGCCTATGGAGTA | 23603 |
rs546835324 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703103 | TATACAAAAGCCAAC[A/G]TACAGCCAGCTGGTC | 23603 |
rs546881357 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705608 | GAAGAAGGGAACACT[G/T]TCAAACTAATTGTAT | 23603 |
rs546893530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712399 | GCCAACATGGTGAAA[C/T]TCCATCTCTAGTAAA | 23603 |
rs546899073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705206 | AATGTAGGCCGGGCA[C/T]GGTGGCTCACGCCTG | 23603 |
rs546899332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696418 | GTCGGGGGGAGGGAG[A/G]GGACGGGGGGGTTGT | 23603 |
rs546935978 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704419 | GGAGGCTTCAGTGAG[A/C]CAAGATCGCACCACT | 23603 |
rs546945731 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108709517 | TTCCTCTTCTTAAGA[C/G]AGCTGTCTGCATTGT | 23603 |
rs547003557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108688859 | AAATGGTGAAATCTC[A/G]TCTCTACTAAAAATA | 23603 |
rs547016005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108672956 | ATTCCTGTCTCTTCC[C/T]CTCCTTGGGCCTCCC | 23603 |
rs547031581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664035 | ACAAACAACCTCTAA[G/T]AAAAGGGCTGAGTTA | 23603 |
rs547037116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717199 | GTCCCAGCTGGGAGG[A/G]ACAACAAAATATCAA | 23603 |
rs547053098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680256 | GGGTCACAGTCTCTG[C/G]AGAGGTTTTCTTCTG | 23603 |
rs547071595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702617 | ACATGGTTCAACATC[A/G]ACAACTCAGCTGAAA | 23603 |
rs547074825 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108673896 | TAATAAAATAAAAAA[A/T]AAATAAATAAATAAT | 23603 |
rs547112186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710306 | TGATACTGAAGGCCA[A/G]AAAGGAGGATTACGG | 23603 |
rs547183933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678499 | CACCCAAAACTCTCA[A/G]TTTTCTAGATATGAC | 23603 |
rs547190786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656894 | CTAATCTCAAGTACC[A/C]AGGGACACAAACACT | 23603 |
rs547222542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678166 | AAACTGCTATAACGT[C/T]CTGCTTTTCAAGCCT | 23603 |
rs547299560 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669328 | AAACTGGTTCTACTG[G/T]ATTTTTCTATGAAAT | 23603 |
rs547309544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686921 | GGCACAAGGGAGAGG[C/T]GTAATGGCACAATTT | 23603 |
rs547344302 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647079 | ACGACACAATCAGAA[C/T]TAGTTTGTTTTCTAA | 23603 |
rs547348747 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729583 | CCTAAGGTACAACAC[A/G]ATTCTCAGTTTTATT | 23603 |
rs547361254 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108655899 | TGGGAAGTGAGGAGC[G/T]CCTCTTCCCGGCCGC | 23603 |
rs547367622 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108725821 | TTTATTTATTTATTT[A/T]TTTTTTTGAGACGGA | 23603 |
rs547407476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654865 | CACATGCCACCACCC[A/G]TGGCTAATTTTTGTA | 23603 |
rs547469456 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717321 | AGGTCAGCAGAACCC[G/T]GATCACAGAGGGCTT | 23603 |
rs547552746 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710717 | AACAGGTGTGTGCCA[C/T]CACACCCTGCTAATT | 23603 |
rs547583393 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732090 | TATTCCTAGCATCTC[A/C]AGCCCCGCCCACTAC | 23603 |
rs547619146 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731507 | AACCGCTGCCGCCTC[C/T]AGCCTGGCACTGAGC | 23603 |
rs547713990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654188 | CCTTGGCTTATAACA[A/T]ACACACACAAATTAG | 23603 |
rs547733644 | snp | C/G | | | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658764 | CTTGTTTCCTGGGAT[C/G]AATGACTCTCACTTT | 23603 |
rs547817303 | in-del | -/TTGT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716652 | ATTTTGGTCCTCTGG[-/TTGT]TTGTTTCTTCATCTA | 23603 |
rs547819104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661603 | TAGCAGGGGAAAATC[A/T]AAGTTTTCTTTAAAA | 23603 |
rs547839283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686063 | GAGGGCTCCAGTTCA[C/T]GGAGATTAAAGGAAA | 23603 |
rs547839323 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108712294 | TAAGAAGATGGAGGC[C/T]GGGCAGGGCGGCTCA | 23603 |
rs547848640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695334 | GTTACACAGGCTAGC[A/C]CTATTCAGTGTTGGA | 23603 |
rs547860536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700231 | TGCATCCTCACCAGC[A/G]CCCAGCCCTTATCAC | 23603 |
rs547865467 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | CORO1C | GRCh38.p7 | 12:108657066 | TAAAATTAAAAAAAA[A/T]TAAAAAAATAAAAAA | 23603 |
rs547882323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693123 | TTCTATATCCTCCCC[C/T]CTAAAGAAAAATTCG | 23603 |
rs547896983 | in-del | -/TAAA | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108653723 | TTATCACCCCTGAGC[-/TAAA]TTTAGTCAGGCCTCA | 23603 |
rs547929566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714887 | GGAACTTCTTACAAA[C/G]AGACTTGGTTGGGGA | 23603 |
rs547980829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671877 | AAGAGGTCCTCCCAC[C/T]TCAGGCTCCCAAGCA | 23603 |
rs547988939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669024 | CAATTTACACAACTG[C/T]TGTGTGATAGTATAA | 23603 |
rs548004732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649364 | ATGAAAAAATTACCA[G/T]GTCAACCTACAGGAG | 23603 |
rs548032947 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656624 | AGGGGAAAAGGTGGG[A/G]AAAGGATAGAGAAAT | 23603 |
rs548098399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108679356 | ATAAAATGCTTAATG[C/T]TGGTCATAAATAGCT | 23603 |
rs548234830 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704134 | TGCTTTGTCTTCATT[A/G]AAAGATACTATACAA | 23603 |
rs548293668 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108715821 | ATAGACATGAGTGAC[C/G/T]TAGCAATCTCACTTA | 23603 |
rs548301829 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671135 | GCCACAAGTTAGAGG[C/T]CAGCCTGGACAACAT | 23603 |
rs548307242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647626 | TTCTATTTTGCAAAC[A/G]GCAAGCCATAGTCAC | 23603 |
rs548317027 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729634 | TTATGCGATTTCTCA[C/G]ATCCAATGTTTACTA | 23603 |
rs548346736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687583 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 23603 |
rs548366033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651495 | ATCAAGCTAACCTAC[C/T]GCCCCATTATAGGAC | 23603 |
rs548387909 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108717603 | AGTCAACTGAATTTA[A/G]AACTGTTTTAGATAT | 23603 |
rs548392260 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733245 | GGGCAGTCCACGGCT[C/T]ACTGCAGCATGGACC | 23603 |
rs548470870 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108691234 | GAAAGCAGACATGTG[C/T]CCCATCACATGCCCT | 23603 |
rs548482880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717951 | GGCCGGGCACAATGG[C/T]TCACACCTGTAATCC | 23603 |
rs548504180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108708174 | AAACAAATACTTGTA[C/T]ATGAGTCTTCATGGA | 23603 |
rs548518833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717255 | GTCAGAATCTGGACT[A/G]CTTAGCCCACAGAGG | 23603 |
rs548524417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108726335 | GAGGCGGGAGAACGG[C/T]GTGAACCTGGGAGGC | 23603 |
rs548541800 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108716356 | TGAAATTACTGGATG[C/G]TCATATCTTAAAAAG | 23603 |
rs548553374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687096 | AGCCGAGTTCCTGGA[G/T]ACTGATACTTCAACT | 23603 |
rs548606202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709173 | AAATGAGTGAATTGT[C/T]TAGTATGTGAATTAT | 23603 |
rs548615326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678605 | AAATCCCTAGAACCA[A/G]AAAGATGTAACCAAC | 23603 |
rs548663559 | in-del | -/CAGG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719249 | GCCAGCAAAAAGATC[-/CAGG]CAGGGGCTTCCTATC | 23603 |
rs548698992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677923 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATCACTTG | 23603 |
rs548777465 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726214 | TGAGGTCAGGAGATC[A/G]AGATCATCCTGGCTA | 23603 |
rs548786750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662307 | TGTTGTGAAATGACC[A/G]TGTTAGGCGGTTTTT | 23603 |
rs548810881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699118 | CTCATCTAAACATGA[C/T]AATTTGTAAAGCAAC | 23603 |
rs548812730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691510 | CTTCTGCTGGCAGCA[A/G]TTGTCAGCCTGCTTA | 23603 |
rs548823776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661700 | GGCTTCTGGCTCCCA[A/G]CAAAGTACACCTTCT | 23603 |
rs548902876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700443 | ATCTAATCTCCCACC[C/T]TGGAGCAGGCTTTCT | 23603 |
rs548920895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653943 | TTGCCCATCCCTGAC[A/G]TAAGTACAGATAAAT | 23603 |
rs548989054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108668271 | AGTGGCACCGAGTTC[A/G]GGAAAACCAAGAACC | 23603 |
rs549032318 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108698627 | GTCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 23603 |
rs549042707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715589 | CATTGCTGAAGAAAC[A/G]TCCCTTGGGAAGACA | 23603 |
rs549062102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670015 | GCAATGCCAATAAAA[A/G]GGCGACATTGAGGAT | 23603 |
rs549089228 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108662494 | TTTTTAAAATGTAAT[A/G]TGTTATCGGAGATCA | 23603 |
rs549191942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707197 | GGGATTGATTGGAAC[G/T]GCAAGGGATCCAAAA | 23603 |
rs549212179 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108688931 | GCTACTCGGGAGGGC[C/T]GAGGCAGGAGAATTG | 23603 |
rs549226467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676457 | GCTTCTTCAAAAGAG[G/T]TTCAGACTCTCCGTT | 23603 |
rs549392241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108713628 | GAGTTCCAAAGCTCA[A/T]CAATTCCAGGCCCGT | 23603 |
rs549421205 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717618 | AAACTGTTTTAGATA[C/T]GAAGGGTGCATCAAC | 23603 |
rs549440686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709285 | TGGCAATTATTATTT[A/C]AGAGCCCAGTAATAG | 23603 |
rs549473632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724973 | ATCACACTGTAACCA[C/G]AAGAGTTATCTCAAG | 23603 |
rs549483048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108653171 | TCCATTTGTCTCAAT[A/G]ACTGAGATATCTAAA | 23603 |
rs549524791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108678453 | ACAGACGTTATACAT[C/T]TTCTCAGGCCCATTT | 23603 |
rs549555856 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108728838 | AAAAGACATACAAGT[A/G]TCAGAAAAGAGTTTT | 23603 |
rs549558891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685956 | TAAGTATCTTCTTAC[A/T]CATAATGAAATCAAA | 23603 |
rs549589354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682881 | AACCAAAAATCTCCA[A/G]TACATTTGAAAATAT | 23603 |
rs549603438 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721670 | ACCAGTAGTTCAAAC[C/G]CTTCACAGAGGCACT | 23603 |
rs549717550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108729554 | CCTCCACCACGAAAC[A/C]CTGCACTTCAAGACC | 23603 |
rs549786407 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108653250 | AAGAATTTTCCATCT[C/T]ATGTTACTAATATCT | 23603 |
rs549805461 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731938 | TCCTCTGAGCCCCGC[A/G]CACTGCCTATCCGAG | 23603 |
rs549841726 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716991 | TCTCATGGAGCTTAC[A/G]GTCCACTGCAGGAGA | 23603 |
rs549993412 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646965 | AAATACAAAGGAAAA[A/C]AAAGCTACTTTTGGT | 23603 |
rs550037617 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108724048 | TTTATCCAAGAGATA[A/T]CATGTATTTTCAAGT | 23603 |
rs550074686 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731361 | GGCGGCGCAGGCACA[G/T]GCTCAGAGGACAGGT | 23603 |
rs550100619 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108660223 | CTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG | 23603 |
rs550105079 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690596 | ACACGGAAAAGTTAA[C/G]ATTTCCTTACTCAAC | 23603 |
rs550110995 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108678015 | CAGAGCAAGACTCCA[C/T]CTCAAAAAAAAAAAA | 23603 |
rs550247366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668920 | TAGCCACAATCTTAA[A/T]ACTCTCTTTGAGAAG | 23603 |
rs550248521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699402 | ATTCATTATGTCTAT[C/T]TTGTGCTTCTTAATT | 23603 |
rs550298649 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646440 | GGGCAAGAAGGAACA[C/T]TCAGCAGTACACGTC | 23603 |
rs550358835 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108722018 | GGCATGGTTTCTTCC[C/T]GATTCCAGGTATCAG | 23603 |
rs550361944 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108676558 | GGGGGGATCACTTGA[G/T]GTCAGGAGTTCGAGA | 23603 |
rs550401143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108713229 | GTTTTGGCTGAAAGA[A/G]ATTTGTATTCCACTG | 23603 |
rs550440768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108729037 | CTAAAGTACCAGTTT[A/G]TGACAAATCAAAATA | 23603 |
rs550509073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108714264 | CGTGGTGGCGCACAA[C/T]TGTAGTCCCAGCTAC | 23603 |
rs550519149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722617 | CCACCACTTACAATG[C/T]TGAATCAACACAATA | 23603 |
rs550541316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705235 | TGTAATCCCCACACT[C/T]TGGGAGGCCGAGGAA | 23603 |
rs550564624 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644863 | CCATCCCAGGACACA[C/T]CGCTGGCAAAGGTCT | 23603 |
rs550582741 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108683019 | AGATCTTAGTGAAAA[A/C]TGGACAGTCTTAAAT | 23603 |
rs550638820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712514 | AGGAGGTGGAGGTTG[C/T]AGTGAGCCAGGATTG | 23603 |
rs550646605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684025 | CAAATTCAGCAGTGT[C/G]AGTTGTTCTTTAAAA | 23603 |
rs550666211 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675180 | CAGTATTTTTAAATG[-/TA]TATATATATATATAC | 23603 |
rs550684574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720084 | CCAGCTACTCGAGAG[A/G]CTGAGGTGGGAGGAT | 23603 |
rs550711766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673999 | GGTTTACTGAATATT[C/T]TAAGCCCACCATTGA | 23603 |
rs550758188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659373 | TACGCTCCTTCCTTT[G/T]AAAGAAAACTTTGAT | 23603 |
rs550787976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688634 | AATCTAAGCTGGGCA[C/T]GGTGGCTCACACCTG | 23603 |
rs550792150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696261 | AGGGAGAAAGAAAGC[A/G]ACTTGGGAAGACAGG | 23603 |
rs550795348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658581 | AGAGAAGCACAACTG[A/G]GGAGACAGAAGCCTT | 23603 |
rs550859644 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108727342 | ACCCATGTCCCAAAG[G/T]ACAAGTGGGATTCTA | 23603 |
rs550901426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652165 | TACTACTTTCTTGCT[C/T]AGAATGGTCAGATAT | 23603 |
rs550970354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665643 | GATGATCCTGGCAAA[C/T]ATCACTGCATAGAGA | 23603 |
rs551090473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730522 | CCCACCCTCCACGTC[C/T]GACCTCATCCTCAGT | 23603 |
rs551133966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108666574 | GGTGATGGCCTGCTC[A/G]GTTTGGACTGATGTT | 23603 |
rs551135064 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704248 | TTTGGGAAGCTGAGA[C/T]GGATCACGAGGTCAG | 23603 |
rs551146971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668514 | AAATGCCTTCCCACC[C/T]GCCAAAAAAAACTAT | 23603 |
rs551211654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706510 | TGTGTGCTGAAGACA[C/T]GATCTTATATACAGA | 23603 |
rs551243473 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644978 | AGCCACCCACACGCG[C/T]TTCCCCTGTACTTAC | 23603 |
rs551271341 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693233 | CACAAACAACCTCAC[A/G]GTCTTGGACAACCAC | 23603 |
rs551377274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108675494 | ATGAAAGGAACGGGG[A/G]AAAAAAAACCCTAAT | 23603 |
rs551392123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108676605 | GATGAAACTCCGTTT[C/T]TACTAAAAACATAAA | 23603 |
rs551393789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684565 | AAAAGTTTAAGGCAC[A/G]CGAAATAAAAGTACA | 23603 |
rs551398446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690951 | GGAGATTGATCTACT[A/G]AAACCCTCTGTGAAC | 23603 |
rs551444566 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666358 | GAAATGAAATAAGAA[A/G]ACAACAGAATTCTTG | 23603 |
rs551479716 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668145 | ATACATGAGACAGGA[A/G]AAAGCTTAAAGATGT | 23603 |
rs551592729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680992 | TTTTGAATGTGTGCT[A/C]TCTTTCTCCTTCCTT | 23603 |
rs551622357 | snp | A/T | 1.66164e-05 | 0.00288235 | intron-variant | CORO1C | GRCh38.p7 | 12:108652441 | AACCAGAGACAAGTC[A/T]GTGTCTGATTGTTAA | 23603 |
rs551663960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698492 | AGCTCACTGCAACTC[C/T]GCCTCCCGGGTTCAA | 23603 |
rs551706578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720759 | CGACATCCTGACCTC[A/G]TGATCCACCCGCCTC | 23603 |
rs551713113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108650351 | ACCTGGCTAATTTTT[C/T]TAATGTTTTGTAGAG | 23603 |
rs551746997 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645604 | ACACACACACAAAAC[C/T]ACATCAAACATTCAG | 23603 |
rs551756878 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721982 | CTGTTTTGGAGTGAC[A/G]GGAAGAACCTTTCTA | 23603 |
rs551776399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657787 | TAGGCATGCCCTACC[A/G]TTTCTACCAATATCA | 23603 |
rs551795591 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691082 | ATAAATAGAAAAATA[C/T]TACAACTTTTTTTGG | 23603 |
rs551814158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108728107 | ACTCTTGGTGAATAC[C/T]GTAAAATGGTGCAGC | 23603 |
rs551997303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696344 | TATAATTCTTACCGA[A/T]TCCTCCCCCTCTTAC | 23603 |
rs551997883 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692942 | AGCTGCGATAACAGG[C/T]GTGTGCCACCATGCC | 23603 |
rs552040306 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681496 | ACTGACAGAGTAATT[A/G]GACTGATTGTGAGCA | 23603 |
rs552086064 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | CORO1C | GRCh38.p7 | 12:108657075 | AAAAAATTAAAAAAA[A/T]AAAAAATATATAGTC | 23603 |
rs552103449 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108702046 | ACGGGTAAGAGCCAG[-/C]GTCTGGGAAAAGCAG | 23603 |
rs552193352 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687544 | AATCTCAGCACTTTG[A/G]GAGGCTGAGGCGGGC | 23603 |
rs552193464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108661668 | AAGCTGGCAGCAACA[C/T]CACAGAGGGAACACA | 23603 |
rs552278365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108656419 | CCAGCAGCCCCATCC[A/G]GGAGGGAGGTGGGGG | 23603 |
rs552377923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108726371 | TTGCAGTGAGCTGAG[A/T]TCGTGCCACTGCACT | 23603 |
rs552392243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709987 | AAGGAATATTTACAA[A/G]TTTCAAAATAAACTT | 23603 |
rs552425831 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707931 | AAACCACAATGAGAG[A/T]CTATTCCATACCCAC | 23603 |
rs552458803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719175 | TTGGACATCACAATA[A/G]TAACTAAAGAGAAAT | 23603 |
rs552509921 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733285 | CAAGTAATCCTCCCA[C/T]CTCAGCCTCCCACGT | 23603 |
rs552595877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679399 | TCATGTCACACATTT[C/G]AATCTAGCAAACCAA | 23603 |
rs552597092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702527 | CAATGTAATTTTCCT[A/G]TGTGCTACTGCAGGA | 23603 |
rs552597769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688422 | GTGGTGTATTACACA[C/T]GTACCGCAGCCATGT | 23603 |
rs552641527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648542 | GACGCCCTGGACCAC[A/G]AGGGCTTTCTAGAGG | 23603 |
rs552660043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680030 | TATTAGTTCTTCTAG[A/T]ACAATAATTTACTCC | 23603 |
rs552740598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649612 | CACTGTAATACTGGA[A/G]GAAGGGAGCAAAGAG | 23603 |
rs552750798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648871 | AGAGACATTTGGCAC[C/T]CGTGGGTAAGGAAGA | 23603 |
rs552764557 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CORO1C | GRCh38.p7 | 12:108656325 | CCAGCCGCCCCGTCC[A/G]GGAGGGAGGTGGGGG | 23603 |
rs552788588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108719606 | CCCTAAGGCCTGCCC[C/T]ATGATTTCTCTGGTG | 23603 |
rs552856761 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672700 | TTTATCAACCCTAAG[C/G]CAAGTCTATCTGCAC | 23603 |
rs552882239 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671919 | AGGCACTCACCACCA[C/T]ACCCAGCTAATTTTT | 23603 |
rs552919346 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | CORO1C | GRCh38.p7 | 12:108700325 | GGCCCTCTTCACAGC[-/T]TTTTTTTTCTTCATT | 23603 |
rs552979460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689136 | ACCCGGAAGGCGGAG[A/G]TTGCAGTGAGCTGAG | 23603 |
rs553042811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681160 | TGTGTGCCACCATGC[A/G]TGGCTTGAATGTGTG | 23603 |
rs553125812 | in-del | -/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732937 | ATAATAGTAATATAC[-/T]TTAGAAGAGTTCCTG | 23603 |
rs553135217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108657216 | AACTACACTAAGAAT[A/C]CCATAATCTACTTAC | 23603 |
rs553138422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727547 | GGGTAAAGGTGAGGT[C/T]ACCAGAGGATTTGAA | 23603 |
rs553161241 | snp | C/G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703458 | CTGGAAAAGAGGCTA[C/G/T]AAGAGAGCAAATGTG | 23603 |
rs553209440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710579 | TTTTTTTTTTCTTTT[C/T]TTTTGAGACAGAGTC | 23603 |
rs553244879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694893 | TTGTGTGAACTAACA[G/T]TATGAGTCACGTAAT | 23603 |
rs553245728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726044 | TTGGCCGTGTTGGCC[A/G]GGCTGGTCTCAAACC | 23603 |
rs553324653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695488 | CTAACCATTCCCTCC[A/G]TTAAGTGAATAATAA | 23603 |
rs553568010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693868 | AACCTGAATTCAAAC[C/T]GAACCTTCTCTGTGA | 23603 |
rs553592140 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715649 | CCTCCCCCCCTCCCC[C/T]CCGCATACTCACAAC | 23603 |
rs553623253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717056 | ATGCCGCTGTGGCAA[C/G]TGCTGGAATGCAGAA | 23603 |
rs553624359 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686524 | AATCTAGAATATTAC[C/T]ACTTTTCTGGCATGA | 23603 |
rs553644915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708737 | AAAGTGCTGGGATTA[C/T]GGGCGTGAGCCACCG | 23603 |
rs553654620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724111 | AACCTGGACCAAACT[C/T]CACAGTTTAATACAT | 23603 |
rs553674658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671341 | AAAAAAGAAAGAAAA[C/G]GAGTGGGGGGAGGAA | 23603 |
rs553715339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108678868 | GGCTCACGCCTATAA[C/T]CCCAGCACTTTGGGA | 23603 |
rs553742376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108661895 | GAGCAGTGCACCCCA[A/G]TACTCTTCACCATGG | 23603 |
rs553769420 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669084 | GGTAAACTGTGTCAA[C/T]ATAATTTAATTTTAG | 23603 |
rs553793390 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647302 | GAATGTCTCCAAATG[A/C/G]CAGTGCCTCCCTTTC | 23603 |
rs553814014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715875 | GGGGTGGCTCACACC[C/T]GTAATCCCAGCACTT | 23603 |
rs553937472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653344 | TTAACACCTGTTAAC[A/G]TCTGCAGTAAAATGG | 23603 |
rs553938120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108647837 | TATAGGACAAAACAG[C/G]CTCCTTCAACAGTGT | 23603 |
rs553939293 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645390 | TCTCTTTGAACCACA[C/T]GCCCTACGGTGTTTC | 23603 |
rs553951442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652701 | GCACCAGGCCAGGGT[C/T]AGGGCAAAAATGTTA | 23603 |
rs554019301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694904 | AACATTATGAGTCAC[A/G]TAATACAGTCTAAGA | 23603 |
rs554074764 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108654538 | TAGAATAACAGAAGT[C/T]TGAACTATGCACATA | 23603 |
rs554091583 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108660356 | CTTGGGAGGCTGAGG[A/C]AGGAGAATCGCTTGA | 23603 |
rs554178945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730326 | TTCCAGCGTTCAAAA[C/T]CCTTTGAACACTCCC | 23603 |
rs554194935 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668196 | ACAGCGTCCTACAGA[C/T]GCCCACAAAGGCCTG | 23603 |
rs554206631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108688026 | CCTCCCAGGTACAGG[C/T]GATTCTCCCGCCTCA | 23603 |
rs554292017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648136 | TTGCCAGCCCCACAC[C/T]GCCAGATCCTTCTGT | 23603 |
rs554366801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706711 | GCGATTCTCCTGTCT[C/T]AGCCTCCCGAGTAGC | 23603 |
rs554468559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698703 | TGGGCCACTGTGCCC[A/G]GCCAGAAAATAACTT | 23603 |
rs554543477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108701747 | CGAAAAACAAGTTAC[A/G]ATTTTGTGGCTTTGT | 23603 |
rs554553284 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651876 | TGATAAAAAGTGAGA[A/T]GTGCCGGGTGTGGTG | 23603 |
rs554566241 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678826 | GGAAATGAATGGCAC[C/T]ATTAAAATGTAAAGG | 23603 |
rs554657027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678196 | TCTATACATACACAC[A/C]CACCCACACACATGC | 23603 |
rs554701926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708763 | CACCGTGCTCGGTCT[A/C]TTTATTATTTTTTTA | 23603 |
rs554744074 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646036 | GATGGAGAGGCAGGG[A/C]AGGTTAGTTGTGCGG | 23603 |
rs554748548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655424 | CTTTCCACGCTCTCC[A/C]TCTGATGCCGAGCCG | 23603 |
rs554775002 | in-del | -/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730970 | CGTTCCCTGGGGCGG[-/C]CCAAACCCAGTCCCC | 23603 |
rs554782205 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663479 | GCGACATATTCATAC[A/G]CTGGAATATTATTTG | 23603 |
rs554812508 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724128 | ACAGTTTAATACATG[C/G]ACAACCTGAATATGT | 23603 |
rs554962082 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731086 | TAAAAGCCTTCCCTG[A/G]GCAGCCTCGTCCCAC | 23603 |
rs555075243 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706215 | AAAAACAAAAAAAAA[A/G]CATTTGACAAAATTA | 23603 |
rs555112110 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108708569 | CAGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC | 23603 |
rs555116572 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108729240 | TTTTATCAAAAAATC[C/T]AACGGTGTTTAAAAA | 23603 |
rs555207645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685311 | ACTAGAGCTCAACAT[G/T]TTCTCTGGAACCTGA | 23603 |
rs555239323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722124 | TGACTGAATGCAAAC[A/G]TTTCAAAGAGACAAT | 23603 |
rs555244990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108691920 | ATCAAAAATAGCCCC[A/G]GGGTACATTGGGAAG | 23603 |
rs555269174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693242 | CCTCACGGTCTTGGA[A/C]AACCACTCAATTTGG | 23603 |
rs555275915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108730108 | CATTCAATTCTTTTC[A/G]AATGTCTTATAGGAG | 23603 |
rs555297483 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108714361 | GCCACTGCACTCCTC[C/T]AGCCTGCAGCCTGGC | 23603 |
rs555308041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108692649 | CTGTGTCCTCACAAG[C/G]CATGGTATAGACCAA | 23603 |
rs555363930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714130 | GCACAGTGGCTCACA[C/T]CTATAATCCCAGCAC | 23603 |
rs555439051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108668626 | AGAGAAGGGAGAAGC[A/G]TCCTTTAAACTTAAA | 23603 |
rs555446013 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108697959 | AGGCAGTCAGCCCCA[A/T]AGAGAAATGTAGGTT | 23603 |
rs555463614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661101 | TTTAAGTATATATTT[C/G]CTAAGTTTCAACAAA | 23603 |
rs555508592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663465 | TGGCTGAACAAAATG[C/T]GACATATTCATACAC | 23603 |
rs555512681 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693497 | TTATTCTAGTTCTTT[G/T]CCCCATAACAATCAA | 23603 |
rs555543688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108682443 | ATGCACTATTAGCGA[C/T]TAATGTCACTATCTG | 23603 |
rs555564761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683387 | TCGCACCATTGCACT[C/T]CAGTCCGGGCAACAG | 23603 |
rs555569092 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722466 | CAGGGAGGCTCCTGG[G/T]GCATGGGGCATGAGT | 23603 |
rs555578105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675051 | GTATGACAAACTTTA[C/T]TGTCGTGGTCTCATC | 23603 |
rs555584597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108690080 | CCCCTGCTGCTCCAC[A/G]GGGAGGAGCTAGAGT | 23603 |
rs555590056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676035 | AGAAAATGATGAAGG[A/C]GGAATCTTTAGATTA | 23603 |
rs555600569 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700884 | CCATGCTCACAACAT[C/T]GTTATAATAATTTTT | 23603 |
rs555614663 | in-del | -/GTGA | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108683808 | CAGATGGTTTTACAG[-/GTGA]GTGTCACCAAATATT | 23603 |
rs555651259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108667957 | GTACAATTAGTTAAA[C/T]AGTTTTATTTTTCAA | 23603 |
rs555655946 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704733 | ACATGTGGCATAGCC[A/G]CTTTTCTTGCACAGA | 23603 |
rs555687031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714638 | ATGATGGCGCATGCC[C/T]GTGGTCCCAGCTACT | 23603 |
rs555733348 | snp | C/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657716 | TGTGAAAATAAAACA[C/G]ATGAAAGGACTCTGA | 23603 |
rs555734856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651645 | TGCCCACCAGGGAAC[A/G]CTGACCATGGCCTCA | 23603 |
rs555780512 | in-del | -/AC | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108661835 | CGAAATGGCCTTGAA[-/AC]ACACACACGTGCACA | 23603 |
rs555864697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708590 | CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG | 23603 |
rs555886774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720160 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGCAAG | 23603 |
rs555900332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108657015 | ACCCTGCCAAATCCC[C/T]CTCTGCAAGAAACAC | 23603 |
rs555988270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108690176 | ACGGGTGCACACAAT[A/G]TATGACTTGTGCACA | 23603 |
rs556042284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712703 | ATATAAAAATTTGGC[C/T]GGGCACGTTGGCTCA | 23603 |
rs556047873 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730796 | CCAGCTCTGCCCCGC[C/T]CCGCCTGACCCCCAA | 23603 |
rs556117853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698605 | AGAGACGAGGTTTCA[C/T]CACGTTGTCCAGGCT | 23603 |
rs556137578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108669312 | TTACAGTTCATTTGA[A/T]AAACTGGTTCTACTG | 23603 |
rs556150873 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647848 | ACAGGCTCCTTCAAC[-/A]GTGTCCTACGTCCTA | 23603 |
rs556207726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712053 | AAGCGTTCAGTGGGC[A/G]GAGAATGCTCCCTCA | 23603 |
rs556240454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691636 | CCATTCTCTGAGCCA[C/T]CCGTGCAGCCAATCA | 23603 |
rs556242388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683624 | ATATAAAATTGAATA[A/G]TCTAGATGAAATACA | 23603 |
rs556244041 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645832 | TGGCACTACACATTT[C/T]ACGTTCAATCACAGA | 23603 |
rs556252897 | in-del | -/CCAAGGATAGTATCTAAAAGGTGAGACAT | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108714468 | ACACACACACACACC[lengthTooLong]CCAAGGATAGTATCT | 23603 |
rs556257199 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718981 | AAGACAAATAAACAC[A/G]GCCCACTTTCAGAAG | 23603 |
rs556257727 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646676 | GAAAAGAAGAAATAC[A/G]ACGTGAGCTTTTTTG | 23603 |
rs556316116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659824 | TTTAAATGAAGAGAA[A/C]AATAGGCCAAGACTG | 23603 |
rs556317010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668685 | ATTAAGACTATCATT[G/T]TGCAATATCTTTCCA | 23603 |
rs556354780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659010 | GTGAGAATACACATA[C/T]GTATATGCAGAGAGA | 23603 |
rs556441351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705490 | AAAAAAAAGAATGTA[A/G]ACCAACCACAGACAA | 23603 |
rs556502736 | in-del | -/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731566 | CCACCGCCCCCGCCA[-/C]CCGCGCGTAGGCCCC | 23603 |
rs556543903 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645164 | GTGTTTTGACAGAAC[A/G]CTATGGCCACTCTAT | 23603 |
rs556596955 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686133 | CATCATTCTGAAAGA[C/T]ATTTTGCACTAGGAT | 23603 |
rs556759416 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672410 | CGTTTAGTTTTTTAA[C/T]GATTTTCAGTATCAT | 23603 |
rs556793154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698104 | ACACTCCAGGGCTCA[C/T]GGGCCAAGCCCTGCC | 23603 |
rs556829884 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | CORO1C | GRCh38.p7 | 12:108706197 | GAATCAAAAAAAAAC[A/C]AAAAAAACAAAAAAA | 23603 |
rs556860222 | in-del | -/CCAC | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108706382 | ATAAGATGAGCTTGT[-/CCAC]CCACCCTTGCCACTT | 23603 |
rs556879224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108728297 | ACTGATGAATGGATA[A/G]ACAAAATACGGCATA | 23603 |
rs556909598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675126 | TCAACACTGAGGGGA[A/G]ACCCTCCACAGCAAA | 23603 |
rs557023410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711262 | GCGGTCCCAGCTACT[C/T]GGGGAGCTGAGGTGG | 23603 |
rs557091800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712725 | GTTGGCTCACGCCTG[C/T]AATCTCAGCATTTTG | 23603 |
rs557118287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720212 | CAGACACACACACAC[A/G]CACACACAAACTTGC | 23603 |
rs557190249 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703563 | GAGTCTCAGGAGGAG[C/T]GCACAAAAAGGACAT | 23603 |
rs557220117 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108718578 | AAAGAAAAGAAAATG[A/G]AAACTAACACTGTTT | 23603 |
rs557230737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696429 | GGAGGGGACGGGGGG[A/G]TTGTATGTGTATCTA | 23603 |
rs557284138 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733509 | AAAAGTTGTTTTTTT[A/T]AAATCCACTAGTTAA | 23603 |
rs557390202 | snp | C/T | 3.30049e-05 | 0.00406219 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657336 | GCTGCCGCTCGCTCA[C/T]GCGGCTGAACCCAGT | 23603 |
rs557405987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664173 | TAAAACAAGTAAATT[C/T]ACCATCAGAAAATGA | 23603 |
rs557409046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687278 | TTCCTCTTTAGGCAC[A/G]CTAAATTCAACATAA | 23603 |
rs557447770 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691779 | ACATATCAGTGAACT[A/G]CAGCAGCAGGAGAAG | 23603 |
rs557474247 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108720275 | CCCATGCTGCCAATA[C/G]TTTTAATTTATTCAA | 23603 |
rs557502911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667144 | TATGACCACTATGAC[A/G]CCATATATATTTCTA | 23603 |
rs557519652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680279 | TTCTTCTGGGAAAGG[C/T]AAGTTCTAAGTTGAG | 23603 |
rs557526465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657946 | GGGCTCAGTAAGCAC[C/T]AGCTACTATCATTGC | 23603 |
rs557547761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696290 | GGAGCCATCTAGTTC[A/G]CATCCTCCAGCCAAG | 23603 |
rs557563720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714302 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCGGGA | 23603 |
rs557584398 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669529 | TAAGCGAAGCGACCT[A/G]CAAATGCTCAGAACT | 23603 |
rs557584852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673099 | AGAAATGATTAAGCT[C/T]AGTGAGGAAGCCATG | 23603 |
rs557688092 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704546 | GGATAGAATGATATA[A/G]AAGTTCTTTTGCTAC | 23603 |
rs557703374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108721362 | TAGGCACACCCTCAG[A/G]CAGGATCTCACTCCC | 23603 |
rs557772867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691772 | GCTGTGGACATATCA[A/G]TGAACTGCAGCAGCA | 23603 |
rs557811445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728401 | ACCTTGAAAATATGC[G/T]AAATAAGGGCAAGAC | 23603 |
rs557815060 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667198 | GAATGAGTCTTGTCT[C/T]CAAATTAATTCAGCA | 23603 |
rs557818259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675868 | GAACCTGAATCTGAC[C/T]GCACTTCAGGTTCCA | 23603 |
rs557883626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108706282 | AATAGAAGGGAATTT[C/T]CTCAACCTGATAATG | 23603 |
rs557920484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714091 | ATGTGCTCAGTTGTC[C/G]AAGAAAAGAACAACC | 23603 |
rs557957863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689282 | TATGTTAAAGTCGCA[C/T]AACGCTTTACCCAGC | 23603 |
rs557981374 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108690023 | CTTTTTCTTATGACA[A/G]TATTATTTATGTGGA | 23603 |
rs558009243 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658179 | AACTTGTTGCTTTTC[A/G]CCCTGCGCATTTATT | 23603 |
rs558046182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660549 | GGATGGACAATTGAA[A/C]CTTCCTCTGCCTTCT | 23603 |
rs558062660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711277 | CGGGGAGCTGAGGTG[A/G]GAGGACTGCTTGAAC | 23603 |
rs558071395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726807 | GACTAAATCGTGTTC[A/G]CTGGCCATCTACCCT | 23603 |
rs558099993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673215 | AAAGTGCTACTCCAG[C/T]GAACACATGAATGAT | 23603 |
rs558175178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688036 | ACAGGCGATTCTCCC[A/G]CCTCAGCCTCCTGAG | 23603 |
rs558178454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108650981 | TTTGTTTGTTTGAGA[C/T]GGAGTCTCGCTGTGT | 23603 |
rs558238559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679722 | CCAGGAAAGCAGAAC[A/G]TTAACGTGTAAAGAC | 23603 |
rs558324354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108648304 | AGACAGGAAAAACCC[A/G]AGAGGCTCCTGTTCA | 23603 |
rs558338256 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CORO1C | GRCh38.p7 | 12:108656108 | CCTCTGCCCGGCAGC[C/T]GCCCCGTCTGAGAAG | 23603 |
rs558352106 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721073 | AGGTGTTCACTTTCA[A/C]AAACTGTAAAATAAT | 23603 |
rs558387027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665797 | GATTATGGGCTCTGG[A/C]CAGACTGATGTGACT | 23603 |
rs558458348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719499 | GGTGCACAATTCACC[C/T]TATCTTAACTTACTC | 23603 |
rs558551729 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675807 | CATGTGCTTCCTAGC[A/G]TATGGAAGAACATAA | 23603 |
rs558603279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702784 | GAATTTATTTTTGCC[A/G]GAGTCTCTTACCCTT | 23603 |
rs558617567 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718926 | GAAAACAGCACACAT[C/T]CAATTTCACCAATAA | 23603 |
rs558672786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108671282 | TCAAGGCATGATCGT[A/G]CCACTGTACTCCAGC | 23603 |
rs558682889 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732320 | ACCCCAAAGAGGGCC[C/T]GTGATTGACCCCATT | 23603 |
rs558744828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710460 | TAAATTTTTAATAAG[A/G]AGATAACACACTCCT | 23603 |
rs558776895 | in-del | -/G | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731236 | GAGCCCCCGACAGCA[-/G]CCCCCGGCCCTAACC | 23603 |
rs558827583 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679657 | CTTAGCAATTTTTCA[A/G]GAACAGAAATTTCTA | 23603 |
rs558905344 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647265 | GGAATGTGGCCTATC[A/G]CTGGTTGACAAATCT | 23603 |
rs558913029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724298 | CTGGGTCAAAGACTA[C/T]AAAGGGAAAGCCATG | 23603 |
rs558939638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670425 | AAATCACCCACAGCG[A/G]GCTCCCTTCCAGGAT | 23603 |
rs558953526 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673456 | AAAAGTACAAGGGAA[A/G]GCAGCAAGTGCTGAT | 23603 |
rs559016461 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703168 | CATCTGTACAAGTTA[C/T]AGAAGCTGCAATCCC | 23603 |
rs559074715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108663794 | TATTCTAAAACTCAG[C/T]GAATTGTACATTTTA | 23603 |
rs559091374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717361 | TGTTAAGGATTTTAT[C/G]TGTACTTGCAGTCTT | 23603 |
rs559091434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108709757 | TGAAAAAATCCTGAA[C/T]TAACACAATAGGCAC | 23603 |
rs559224799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679259 | CTCTCTGCTATCCTC[A/C]ATCAACAGAAATGCC | 23603 |
rs559265753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678264 | CACACAACACCCTGG[A/G]AGCTTACCATGACCG | 23603 |
rs559318071 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694205 | GAGAAGTGCTTGAAC[C/G]TGGGAGGTGGAGGCT | 23603 |
rs559323820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687559 | GGAGGCTGAGGCGGG[C/T]GGATCACTTGAGGTC | 23603 |
rs559355780 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668063 | CAGCCATAAAAAGGG[C/T]TACACCCCCAAAAGA | 23603 |
rs559386679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108648401 | TTTAATGGGGCTAAA[A/G]GAGCTTTAACTCCGT | 23603 |
rs559401224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726250 | GTGAAATCCCATCTC[C/T]ACTAAAAAATACCAA | 23603 |
rs559529273 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731728 | GCAGGCGGTGCCCAA[G/T]CGCACGCCCCGCTCT | 23603 |
rs559572992 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733004 | ACTGCTGGGACTCAA[C/G]AAAATGAAAGGATGG | 23603 |
rs559655409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709883 | AAGTTCTTAAAACTG[C/T]ATAGGCTTTCCCTTG | 23603 |
rs559676006 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | CORO1C | GRCh38.p7 | 12:108656273 | GCCCGGCAGCCACCC[C/T]GTCCGGGAGGGAGGT | 23603 |
rs559758611 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108656315 | CCCCGCCCGGCCAGC[C/T]GCCCCGTCCGGGAGG | 23603 |
rs559815709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693762 | TCTTTGCCCTCCTAG[A/G]GACAGAGCCCCTCTA | 23603 |
rs559820912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654636 | TTGACAACATAATGC[A/G]CGCATACATCAGCGT | 23603 |
rs559854433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108692932 | CCTCCCGATTAGCTG[C/T]GATAACAGGCGTGTG | 23603 |
rs559861683 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731175 | CACAGGGACCCTGCT[C/T]CACGCTCCCCACGCC | 23603 |
rs559870062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707190 | GGATGAAGGGATTGA[A/T]TGGAACTGCAAGGGA | 23603 |
rs559906233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723623 | CCAGTTCCACAATGG[A/T]GCAAGAAAGTCTCTT | 23603 |
rs559916473 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725216 | TGCCCTCTTCAGTGA[C/T]TCAACTTTGATTCAA | 23603 |
rs560010480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699816 | GAAAAGATTCATCTT[C/T]GCCAATAAGAAGGTA | 23603 |
rs560012951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685608 | TTTCCACTATGCCAT[A/G]GGTTGTAAAAAAAAG | 23603 |
rs560031050 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702598 | AAATCTAAGTGGAAA[A/T]GGAACATGGTTCAAC | 23603 |
rs560032105 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698982 | TTTCCAATGGCTGTC[A/C]CAGGGCTTAGCTTAT | 23603 |
rs560036633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669740 | TTTGATCTATAATAC[A/G]GTGTTCTTTTACCTT | 23603 |
rs560044864 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680306 | TGAGGCCTGAATATG[A/G]CCCTGTTTACAGACC | 23603 |
rs560080300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709129 | TTTGATTATATATAT[A/G]TACTATAAACCGCTG | 23603 |
rs560146042 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108685627 | TGTAAAAAAAAGGCA[A/C]ACAAGTAATGTTAAA | 23603 |
rs560366253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653821 | CCTCAAAAGTTTGCA[C/T]CCACAAAGCACCATT | 23603 |
rs560373452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692114 | CTGGCAGCTCGTGAC[A/T]TAATTTGGAAGTCAT | 23603 |
rs560398224 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108675510 | AAAAAAAACCCTAAT[G/T]TGTCACCTTCTGAGG | 23603 |
rs560413713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722310 | GTGCTTTGCTACCAT[G/T]ATTTAAAGAAAGTGA | 23603 |
rs560436989 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108682560 | CAAACGTTGACAGAA[C/T]TTGAAGAAAATGACA | 23603 |
rs560452161 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646204 | CTAAAAGGCAGGAAG[A/G]AAAGAAGGAATGGCT | 23603 |
rs560477254 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697765 | TTCTTAGACACAAGT[A/G]CTCCTGGAGGGCACA | 23603 |
rs560543380 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648908 | GCCTGGGATTTTTGA[A/T]TTTTATTTTTACATT | 23603 |
rs560607984 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706816 | CTCGAACTCTTGACC[A/G]CAGGTGATCCTCCTG | 23603 |
rs560608227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660126 | AAAAATAGTCACTAA[C/T]ATCCAGGATACTTAA | 23603 |
rs560645168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668136 | ATGAAGAAAATACAT[A/G]AGACAGGAGAAAGCT | 23603 |
rs560665522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714200 | TTGAAACCATCCTGG[C/T]CAACATAGTGAAACC | 23603 |
rs560685632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108651974 | AGGTTGCAGTGAGCT[A/G]AGATCACACCACTGC | 23603 |
rs560687533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724874 | ACTGTATTTTTGTTA[C/T]TAATGTAAGATCCAA | 23603 |
rs560784452 | in-del | -/TC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681011 | TCTCCTTCCTTTCTT[-/TC]TCTCTCTCTCTCTTG | 23603 |
rs560861974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108693025 | CTGGTCTCAAACTGC[C/T]GACCTCAGGTGATCC | 23603 |
rs560923528 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646911 | GTCCCTTTCAAATTA[A/G]GGAAAAAAAACCACA | 23603 |
rs560937211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660779 | TTTTCCTCTCCTTAA[A/T]CAGACTGAGGTTCTG | 23603 |
rs560951408 | snp | A/C | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731237 | AGCCCCCGACAGCAG[A/C]CCCCGGCCCTAACCC | 23603 |
rs560974051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668878 | ATTTTCTTGGAGCTA[A/T]TATTTCCCCCAAGTA | 23603 |
rs561006373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108679025 | CTGAGGCAGGAGTAT[C/T]GCTTGAACCCGGTAG | 23603 |
rs561017332 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | CORO1C | GRCh38.p7 | 12:108662812 | GAAAATATTACAAAA[-/G]AAAAAAATGAATTAG | 23603 |
rs561037923 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108699277 | GTCTCCCTCAAATGG[C/G]ATAAGTGAAACTCAG | 23603 |
rs561077842 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732616 | CAGAGCCTGGGGAAC[C/T]GAACCGACTGTGGGG | 23603 |
rs561129879 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659079 | TTGTCAGAGGCCCTA[C/T]CAGAGGCCCTACTTA | 23603 |
rs561214192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708215 | ACAAGAGCCAAAGGG[C/T]AGAAGCAACCCAAAT | 23603 |
rs561216736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685864 | CATTTTAAAGGTACA[C/G]TGATTATTTGGCATG | 23603 |
rs561236894 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645494 | TCCTCAGCAGATTAC[A/C]TTGATAAAGAAACAA | 23603 |
rs561240553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723354 | AATGCTTGACCATTA[C/T]GAAAAGGAATTTAAG | 23603 |
rs561272388 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647347 | CCACACCAATAACCA[A/G]CTCCCAAGCACAAGT | 23603 |
rs561285709 | in-del | ATTTTTAGTACGT/GGCTA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654867 | CATGCCACCACCCGT[ATTTTTAGTACGT/GGCTA]ATTTTTGTATTTTTA | 23603 |
rs561386660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108677024 | TTCAGGAATTAATTT[A/G]TATTTATGTAAAATA | 23603 |
rs561458675 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707267 | AGGAAGACTCCTATT[A/C/T]CCTGATTTCAAAACT | 23603 |
rs561477185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706419 | AGGATTGTAGTACAG[A/G]TTCTAGCCAAGGCAA | 23603 |
rs561482250 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645420 | CACCACCATCAACAA[C/T]TTTACTTCATTAATT | 23603 |
rs561527065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652834 | CATTTACTGGCATAA[C/T]GCAATGCTGTTATGC | 23603 |
rs561530587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108688724 | CCAGCCTGGCCAACA[C/T]GGTGAAACTTCATCT | 23603 |
rs561555255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108728493 | GGGGTTTCTTTTTGG[A/G]GGGGATGAAAATGTT | 23603 |
rs561572196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683894 | GTGCCACTGAATTCA[C/T]CATATAAGGAATGTA | 23603 |
rs561619934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697721 | ATGAGGAGACAAACA[C/T]CTCAGTACCAGCAAT | 23603 |
rs561627372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676496 | TGGCATCAGAGTTAG[G/T]CGCAGTGGCTCGTGC | 23603 |
rs561696860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712441 | CAGGTGGGCGTGGTT[A/G]CAGGTGCCTGTAATC | 23603 |
rs561719647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658496 | AGTGAACTGATACAA[A/T]CTATTTCTTTGTGAA | 23603 |
rs561734733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652035 | GTCTCAAAAAAAAAA[A/G]AGTGAGATTTTTTTC | 23603 |
rs561737453 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660879 | AAGTGGGCCTTAGTT[G/T]CAATAGTTACTTGGC | 23603 |
rs561741835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691186 | ACTCAATTCAGTCAG[C/T]CAGAAATGAAACCCA | 23603 |
rs561780364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690712 | TTTCTGCTCATTATT[C/G]CAGACAAGTAATTCC | 23603 |
rs561780471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108698357 | CATAGCTGAGAACCA[C/T]GGAAGGTGAGAAGCA | 23603 |
rs561866434 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108726825 | GGCCATCTACCCTAC[A/T]GAGGAGACTGTGCGC | 23603 |
rs561957542 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714867 | TATAATCTATACTCA[A/T]TTTAGGAACTTCTTA | 23603 |
rs561969612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679518 | CTTAATGCCAGTCCA[C/T]GCTGAAGCTGTGTAT | 23603 |
rs561976991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680769 | TCTGATGGTGTCTCT[C/G]CTTAAAGAACGACCA | 23603 |
rs562024950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696600 | AAAACCTGTGTGCTC[C/T]TGAGACAAGGCAGCT | 23603 |
rs562063475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696098 | AGAAGAGATCATGAC[C/G]CAAAAAGCTAACAGA | 23603 |
rs562155534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108689352 | AGTAATAAATTCCCA[A/T]GGTGATAAAAAGTGA | 23603 |
rs562212867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108681629 | CAAGAATGATGACAA[A/G]AAAAAAGCAAACAAA | 23603 |
rs562214196 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654061 | ATTTTCCCCAATACC[C/T]CAGCCCAACCTCTGC | 23603 |
rs562304522 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698920 | CACAAAAATCTCACA[G/T]AGTACTCATGAACCT | 23603 |
rs562307049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649182 | GAATTTAGTGTTCCC[A/G]GTTGACAGATGAGAG | 23603 |
rs562316014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108714166 | GAGGCCGAGGTGGGC[A/G]GATCACGAAGTCAAG | 23603 |
rs562475651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653683 | GGAAGGTTTTTGGAG[C/T]TCAGTGTGGAGTCTC | 23603 |
rs562483571 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707360 | TATCAATGGAATATA[A/C]TTAAAGTCCAGAAGT | 23603 |
rs562511286 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645477 | GAATCTTAGACAAAA[G/T]GTCCTCAGCAGATTA | 23603 |
rs562521476 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726065 | GTCTCAAACCCCTGA[C/T]CTCGTGATCTGCCCG | 23603 |
rs562577593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108684479 | GGAATATTTATTGCC[A/G]CATTGTTGGAAATAG | 23603 |
rs562665234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660009 | TTAAAAAGAGGCAGC[A/G]TGTGTTGCTCCTAGG | 23603 |
rs562671236 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714281 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 23603 |
rs562699693 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715931 | AAGGTCAGGAAATGA[A/G]ACCATCCTGGCTAAC | 23603 |
rs562742625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652898 | GAAGAAACTCAGTTT[C/T]AGTGAGTATCCTCAG | 23603 |
rs562767075 | snp | A/C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693120 | AGATTCTATATCCTC[A/C/T]CCCCTAAAGAAAAAT | 23603 |
rs562794295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649085 | GACTAACAGGATGAA[A/T]AATTAGTTTTCTACA | 23603 |
rs562808186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676081 | CATATCAAGTTTTTA[A/T]AACTGGCAAGACCAA | 23603 |
rs562836348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706471 | GAGACATTCAGATTG[A/G]AAAGAAAGAAGTAAA | 23603 |
rs562864511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689436 | GGTATCCCACACACA[A/G]TTTCTTTCAAGTTTG | 23603 |
rs562881077 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108729390 | GTTATGTTTCATCGG[C/T]ATGTATCTATTAAAA | 23603 |
rs562881840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108673675 | CTTGTTAGAGGCTCA[C/T]GCAGCTGGTGACTTT | 23603 |
rs563005197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675432 | CTTTGAGATAAGAAT[C/T]ATAATGGATTGAACC | 23603 |
rs563015394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658253 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 23603 |
rs563059993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696700 | AGACTGCTATTATTC[A/G]TCCTCTGAAGGACTA | 23603 |
rs563069836 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694280 | GAGCAAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs563105881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651223 | ATTGTGAGACCAGAA[A/C]AGCAAGCGTTTTAAA | 23603 |
rs563197967 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680067 | AAGAATTAACAAATA[A/T]GTGTTGTGAACTTTT | 23603 |
rs563198852 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108676986 | CCCATGAGGAAAAGC[A/G]GGTAAATGTTTAAAT | 23603 |
rs563209619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108650246 | CAGGCTGGAGTGCAG[C/T]GGCACAAGCTCATTG | 23603 |
rs563238113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108719685 | ACCTCCTCCTTCAGG[A/G]AGAACATAAGGCTAT | 23603 |
rs563274811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718970 | CTAGGGAAGTGAAGA[C/T]AAATAAACACGGCCC | 23603 |
rs563276710 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704158 | TATACAAATCTTCTG[A/G]CTGACATACATACTA | 23603 |
rs563377105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679962 | ATCTGTAAAATAAGT[A/T]AAAAAATTAACCACA | 23603 |
rs563377511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108692108 | GTGTGGCTGGCAGCT[C/T]GTGACATAATTTGGA | 23603 |
rs563396304 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704947 | TATAAAGTTGAAGTG[A/C]TCATTAAATGATCAA | 23603 |
rs563514924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717107 | AATAATCGGGGAACA[G/T]AAGCAGTCAGAGAAG | 23603 |
rs563552225 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO1C | GRCh38.p7 | 12:108716383 | AAAGGGATGGGGGAT[A/G]TTTTTATTAATAACT | 23603 |
rs563565266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673662 | ATGAGCTGCCTGTCT[C/T]GTTAGAGGCTCACGC | 23603 |
rs563571777 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665128 | GGGAGACTTTGTTTA[C/T]AATCAGCATTTCCAA | 23603 |
rs563625976 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108694138 | AATATAAAAATTAGC[C/T]GGGCATGATGGTACA | 23603 |
rs563699698 | snp | A/G | 9.91097e-05 | 0.00703882 | intron-variant | CORO1C | GRCh38.p7 | 12:108648932 | TTACATTTGTTTAAA[A/G]TATGGATTGTCTAGA | 23603 |
rs563751895 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108688311 | AGTACTGAGTACAAT[A/T]AAAAAAACTGTTAAT | 23603 |
rs563900752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662316 | ATGACCGTGTTAGGC[A/G]GTTTTTTTTTTGTTT | 23603 |
rs563936864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671478 | AGGAAAAAAAAAATT[A/T]AAAACTGTAATGCAA | 23603 |
rs563997682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710639 | GCACAATCTCGGCTC[A/C]CTGCAACCTCCACCT | 23603 |
rs564041528 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704995 | GCAGGAGATTCTTAT[A/G]CTATAATAGTACCTT | 23603 |
rs564041585 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108712772 | AGATAGCTTAAGGCC[A/C]GGGGTTCAAGACCAG | 23603 |
rs564078304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712358 | ACAGGTGGATTGCCC[A/G]AACTCAGGAATTCGA | 23603 |
rs564134541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727092 | AATCATTCATTCAGC[A/G]AATATCCAGTAGGCA | 23603 |
rs564200878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705769 | AAAGAATTAGAATTA[C/T]ACACCACAATCAAGT | 23603 |
rs564233017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664752 | GACATGCACTATTTT[C/T]ATTCAAGAATTTATG | 23603 |
rs564312548 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716695 | AGAACTAAAATAAAT[G/T]ATTTCTAGGGTCCTA | 23603 |
rs564321255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673774 | AGGAGATATACCTAA[C/T]GCTAAATGATGAGTT | 23603 |
rs564349411 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688646 | GCACGGTGGCTCACA[A/C]CTGTAATCCCAGCAC | 23603 |
rs564373353 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108690514 | AATAGACCATATTTT[-/A]AAATCAATTAAGAAC | 23603 |
rs564434790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688455 | ACCTTCCCAAACTCT[C/T]GAAATTCAACATTGG | 23603 |
rs564435546 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704081 | CCAGATACCATCTAA[C/T]CTCATAAAAATAGGA | 23603 |
rs564448603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719875 | TGGGATGTTACTTCA[C/T]TGACTCTAAAGTCAA | 23603 |
rs564461027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695868 | AAAAAAAAAAAAAAA[A/C]AAAAAAACAGTCTTT | 23603 |
rs564471201 | snp | A/G | 0.000472701 | 0.0153664 | utr-variant-5-prime, intron-variant | CORO1C | GRCh38.p7 | 12:108702970 | GTCTTTGGTAGAGGA[A/G]ATGGCAAATGATTCG | 23603 |
rs564476727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108649838 | ATCACCAGATCAAAC[A/G]GCTGGTGTGCAAGGG | 23603 |
rs564558013 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108680670 | AATGAGACAATCAAG[C/G]TAAAGAACTTGGTTC | 23603 |
rs564581560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679065 | GCAGTGAGCCGAGAT[C/T]GTGCCACTACACTCC | 23603 |
rs564619353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695043 | AAACAGCTTATCTGG[G/T]TGGCTCTGGCCCAGG | 23603 |
rs564650689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656861 | GGCAGCATGCTCGTT[A/C]AGAGTCATCACCGCT | 23603 |
rs564706174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725683 | GACAAAAAAGTTGAC[A/G]TTTTTCTTTCTCTTC | 23603 |
rs564711744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108656360 | GCCCCCACCCGGCCA[A/G]CCGCCCCGTCCGGGA | 23603 |
rs564734576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108663637 | AGAATAGGCAAATCC[A/G]TAAAGACAGAAAGTA | 23603 |
rs564799203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108663209 | AGAGCCTGCACACAT[A/G]GCTGGTGAAAATGTA | 23603 |
rs564820802 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108687482 | ACAGAGTAAGACCCT[C/G]TTTCAAAAAAATAAT | 23603 |
rs564922997 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674496 | GAGGTTGCAGTGAGC[C/T]GAGATCGTACCACTG | 23603 |
rs564930347 | snp | A/C | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662126 | AGGTTCAGTCAGGGA[A/C]AGGGTGAGTCCATTT | 23603 |
rs564962841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672505 | TGAGATAGATCAGGA[C/T]GTTCTAATTCTTCTT | 23603 |
rs564970601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661566 | TATATATGTTCTCTA[C/G]AGTATACATGTACTA | 23603 |
rs565007973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655495 | CCTGATTCTCCTGCC[C/T]CAGCCTGCTGAGTGC | 23603 |
rs565033875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726193 | GAGGCCGAGGCGGGC[A/G]GATTATGAGGTCAGG | 23603 |
rs565234939 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671034 | CTAAAAAAAAAGAAT[-/A]AAAAAAAAAGGTTTA | 23603 |
rs565250213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108708325 | GAATGAAGTACTAAT[A/C]CATGCTACAACTTGG | 23603 |
rs565252184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716019 | GCCTGTAATCCCAGC[C/T]ACTCGGGAGGCTGAG | 23603 |
rs565289400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715417 | AGGACTTCGAAATCA[C/T]CTCTAGCTCTTCAAT | 23603 |
rs565316586 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731170 | CTCCCCACAGGGACC[A/C]TGCTTCACGCTCCCC | 23603 |
rs565348210 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646992 | TGGTTTTGGCAACAT[C/T]AAAAAAGAAAGAAAT | 23603 |
rs565410482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669502 | TGGAAGGCAACTGGG[A/G]CTGAGAGCGTTTAAG | 23603 |
rs565411134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700170 | GGGATCCACTTCCCC[C/T]GCTGTTTTCAGCAGA | 23603 |
rs565425827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108694325 | AACCCACCACAGGTC[A/G]CTGCACATGCAGGCA | 23603 |
rs565448342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677878 | ACAAAAATTAGCCAG[G/T]TGTGGTAGCAGATGC | 23603 |
rs565456041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722706 | CAACCCAGTCTTGAG[C/T]TGGGGACCAAATGTA | 23603 |
rs565468193 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728236 | AACGTATGTTCACAG[C/G]ATTATTCATAATAGC | 23603 |
rs565520512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677069 | AGCTTTCCAAACAAT[A/G]TTTCAGTCCACAGCC | 23603 |
rs565534148 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696003 | ATATTCCCACACACA[A/G]CTCCTAAAATAAATG | 23603 |
rs565542536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108709559 | AGTGTTTTACCACTT[C/T]AAAAACTGTTCAGTT | 23603 |
rs565578461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678507 | ACTCTCAATTTTCTA[C/G]ATATGACATCGTATA | 23603 |
rs565579746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668951 | ATACTGCTGAAGAAA[A/G]GAACTCACAGAGCCA | 23603 |
rs565587678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655935 | CGTCTAGGAAGTGAG[A/G]AGCGTCTCTGCCCGG | 23603 |
rs565593000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108728797 | GAAGAATTCTGTTTT[A/C]ATACAGAAAAGGTAT | 23603 |
rs565658341 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108656389 | GAGGGAGGTGGGGGG[G/T]CAGCCCCCGCCCGGC | 23603 |
rs565672813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717219 | CAAAATATCAAAAGT[C/T]TGTATCAAAAGCAAG | 23603 |
rs565695298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663285 | GGCAGTTCCTTAAAT[A/G]ATTAAACAGAGTTAT | 23603 |
rs565774510 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647081 | GACACAATCAGAATT[A/T]GTTTGTTTTCTAAAA | 23603 |
rs565791645 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108717336 | GGATCACAGAGGGCT[C/T]TCTAGGCCATGTTAA | 23603 |
rs565811313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108678184 | GCTTTTCAAGCCTCT[A/C]TACATACACACACAC | 23603 |
rs565866432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725113 | GAATAGAGAAGACTG[C/T]CTGAATAGACATTTC | 23603 |
rs565884003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726355 | ACCTGGGAGGCAGAG[C/T]TTGCAGTGAGCTGAG | 23603 |
rs565906251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724147 | ACCTGAATATGTGGG[A/G]AAAAGCAACAACAAC | 23603 |
rs565963000 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660118 | CATTTAGAAAAAATA[A/G]TCACTAACATCCAGG | 23603 |
rs565985352 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646523 | TTTAAAGTGATGAAT[A/G]CAATATGATCCTAGG | 23603 |
rs566062338 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726333 | CTGAGGCGGGAGAAC[A/G]GCGTGAACCTGGGAG | 23603 |
rs566116477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730530 | CCACGTCTGACCTCA[C/T]CCTCAGTCATTTCGG | 23603 |
rs566140519 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731524 | GCCTGGCACTGAGCG[C/T]CGTGCGGGGGAGGGG | 23603 |
rs566141998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686990 | GCATGTTCCAGCCAG[C/T]AACCTTCACCGTGGC | 23603 |
rs566145547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714896 | TACAAAGAGACTTGG[C/T]TGGGGACCACCTAAA | 23603 |
rs566192466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108661060 | TTTTATTAAGGTATA[A/G]CTTACATACAATACA | 23603 |
rs566198326 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650848 | TGAATTCAGTCTATT[C/T]TGAACCATATTTTGA | 23603 |
rs566244137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707590 | GCAAAGGATTCTAAG[A/G]TATGACACCAAAAGC | 23603 |
rs566250007 | in-del | -/ACAG | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108697810 | GCAGGTACTCTGCTT[-/ACAG]ACAATCAAACCAACT | 23603 |
rs566256864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654232 | ATACAACACATTGCC[C/T]GTCCTCTAAATCTCT | 23603 |
rs566284414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108698568 | TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 23603 |
rs566319210 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675382 | GGACTCAGAAATCTT[A/G]AAGAGGTTTCAATGG | 23603 |
rs566353323 | in-del | -/AA | 0.360421 | 0.224293 | intron-variant | CORO1C | GRCh38.p7 | 12:108660452 | GCGAAACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs566361965 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657715 | CTGTGAAAATAAAAC[A/G]CATGAAAGGACTCTG | 23603 |
rs566370648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700273 | ACTCACCAAACTCAT[G/T]TTCCTCCTAAAAGCT | 23603 |
rs566405634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708412 | ATTTATATGAAAGTC[C/T]AGAATAGGCAAATCT | 23603 |
rs566448856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108722083 | ACATGCCTCTGCTCA[A/G]CTTTCCCCTTGAAAC | 23603 |
rs566492899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722821 | TTGAAGGTATGATAT[A/G]TTATTTGTTCTACTT | 23603 |
rs566512666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676632 | TAAAAATTAGCCAGG[C/T]ATGGTGGCGCAGGGC | 23603 |
rs566524690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660358 | TGGGAGGCTGAGGCA[G/T]GAGAATCGCTTGAAC | 23603 |
rs566559045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669032 | ACAACTGCTGTGTGA[C/T]AGTATAAAATGCTGT | 23603 |
rs566572989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668515 | AATGCCTTCCCACCC[G/T]CCAAAAAAAACTATA | 23603 |
rs566602195 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705776 | TAGAATTATACACCA[C/T]AATCAAGTGGGATTT | 23603 |
rs566615889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691002 | ACCCTTCCCATTGCA[A/G]CTCTGCATTGGTTTA | 23603 |
rs566655125 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108706033 | CTCTACTAAAAATAC[A/C]GAAGTTAGCCAGGCA | 23603 |
rs566683269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681863 | TACTATGTAAAACAG[G/T]ACTAATAATACCAAC | 23603 |
rs566685244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108674122 | ACAAGGAGATTAACG[C/T]TGTTTTCACCTGCTA | 23603 |
rs566720312 | snp | C/T | 0 | 0 | intron-variant | CORO1C | GRCh38.p7 | 12:108713448 | TATTAATCCAGGTAA[C/T]AGGTAAGATGCCAAG | 23603 |
rs566761076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720764 | TCCTGACCTCGTGAT[C/T]CACCCGCCTCAGCCT | 23603 |
rs566787344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683305 | GTGCCTGTAATTCCA[A/G]CTACTCAGGAGGCTG | 23603 |
rs566802467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667515 | ATTTTCTTAATTTAA[A/T]TAATGCTGTGTGTTC | 23603 |
rs566834906 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733250 | GTCCACGGCTCACTG[C/T]AGCATGGACCTCCCG | 23603 |
rs566863275 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659477 | TAATCCCACCACTCA[C/G]AGAGAAGATCATTAT | 23603 |
rs566898321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108723895 | TTTGCAATAATAATC[A/G]GTCTTCCAAATACAA | 23603 |
rs566909454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714986 | GTAATGTGACGCTAT[A/G]AAAATGACTGCCGAA | 23603 |
rs566923754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108652477 | ACATCTGGATTATGG[A/G]GGTGTCTCTCTCCTC | 23603 |
rs566937733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722972 | TAAAGCAACAGTGGC[C/G]CACAGAAGAGAGAGC | 23603 |
rs566973646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727373 | GAAGTAGAAAGGCGA[C/T]GAAGTAATAAATTCA | 23603 |
rs566979905 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675239 | AATTTTCCCTTAAAA[C/T]AAACCAGGACTTCCG | 23603 |
rs566985029 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108651585 | TCCACTCATAGGGTA[A/G]GAAAACCACCCACTT | 23603 |
rs567071743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108715638 | CCCGCCTCCTCCCTC[C/T]CCCCCTCCCCCCCGC | 23603 |
rs567074191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108692197 | CCCCCAGCTTTTCAC[A/G]GCCCATACACTTGGC | 23603 |
rs567141497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666806 | TACTCAGGGGTTATT[A/G]GAAGGGTTAAATGAG | 23603 |
rs567146534 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647278 | TCGCTGGTTGACAAA[C/T]CTGAAATGGAATGTC | 23603 |
rs567146872 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704457 | AGCCTGGGCGACATA[G/T]CAAGATTCCATCTCA | 23603 |
rs567198907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720134 | GACGCTGCATTGAGC[C/T]TCAATCACACCACTG | 23603 |
rs567311731 | snp | C/T | 4.94654e-05 | 0.00497295 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654326 | CACATAAGTAAATGA[C/T]GCTGGTGTCAGGGTC | 23603 |
rs567312851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669118 | GTGTAAAGAAGCCAC[A/G]TCTAAAAAATGGGGG | 23603 |
rs567336768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661701 | GCTTCTGGCTCCCAA[A/C]AAAGTACACCTTCTA | 23603 |
rs567373602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661237 | ATCTCCAATTTTAGA[G/T]AAAGGAAAAGATTTC | 23603 |
rs567401095 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730775 | CCCACCCACATTACT[C/G]CAGCTCCAGCTCTGC | 23603 |
rs567401736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707830 | TCAAAGGGACTTGAA[C/T]AGACATTTTCCAAAG | 23603 |
rs567411029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108691607 | TTCTCTTCACCACAC[A/G]CTCCCAGATCCCACC | 23603 |
rs567427615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677437 | TGTTTGTATATCTTT[A/G]TGAAAAGGACTTTCT | 23603 |
rs567444381 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CORO1C | GRCh38.p7 | 12:108730121 | TCAAATGTCTTATAG[A/G]AGGGAAAAGCCTTTG | 23603 |
rs567447793 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | CORO1C | GRCh38.p7 | 12:108698649 | TGACCTCAGGTGATC[A/C/T]GCCCGCCTCAGCCTC | 23603 |
rs567466842 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684838 | ATAATAAAGTTAAGA[A/T]ATACACCAATGCATT | 23603 |
rs567494210 | snp | A/C | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732475 | CGTCAGACTGTGTGA[A/C]CTGGGACAGTTCTCT | 23603 |
rs567517409 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108706646 | GTCACCCAGGGTGGA[A/G]CGCAGTGGTGCAATC | 23603 |
rs567567323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676714 | GAGGTAGAGGTTGCA[A/G]TGAGCTGAGATCACG | 23603 |
rs567623508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108667563 | GACAACACATTACTA[C/T]GGCAATGTTTTGTTT | 23603 |
rs567647896 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645092 | ACAGCCAAGGCGTGA[A/T]ATAAACACAAACACC | 23603 |
rs567661412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706172 | AGTCTGGGCAACAGA[A/G]TGAGACTCTGAATCA | 23603 |
rs567796943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675067 | TGTCGTGGTCTCATC[C/T]AGCCCAACCTTCAGC | 23603 |
rs567835527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720976 | AGCTACTATGCACCA[A/G]GCAATATGCTAGGAA | 23603 |
rs567873520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108720164 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACCC | 23603 |
rs567884447 | in-del | -/AGTT | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108722789 | TTCAGAGAAACACAC[-/AGTT]AGTTCATAACCATCC | 23603 |
rs567905767 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666887 | ACTAGGGAGAAGAGC[-/A]TGGGGCTTTCTTTGG | 23603 |
rs567910319 | in-del | -/CAGAGTCAGG | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108665580 | TTAGAGAGTGAGCAC[-/CAGAGTCAGG]CAGAGTCTGGTTCAA | 23603 |
rs567914323 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659742 | AGCTTTGGGATATTA[A/C]AGATGGTACAACAGT | 23603 |
rs567916534 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695058 | GTGGCTCTGGCCCAG[A/G]GTTTTTCACGAGATA | 23603 |
rs568044339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682936 | TTAAAAATCATAATG[A/G]ATAACAGAATGAAAG | 23603 |
rs568101952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727279 | TGAGGGCAGGGACAA[A/G]TGTCTGCCTGTGAGA | 23603 |
rs568113215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728190 | ACAACCCATCGATTA[C/T]ATTCCTAGGTAAATA | 23603 |
rs568165532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682091 | ATAGCTAGAATTTAA[A/G]AACTGGCTCAATCCA | 23603 |
rs568222502 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655157 | GATCTATTTCCTTCC[A/G]ACACATGTACACAGA | 23603 |
rs568230116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108650827 | TATTGGATGTAATCA[C/T]AAATTTGAATTCAGT | 23603 |
rs568254702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108689164 | GAGATCGCACCACTG[C/T]ACTCCAGCCTGGGCA | 23603 |
rs568257550 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656739 | GGATGTTGTTGATCT[A/G]TGACCTTACCCCCAA | 23603 |
rs568269982 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693160 | CTCAGTAGAAAAAAA[A/T]TTAATAAAAATATAC | 23603 |
rs568270327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695129 | GCTGCAGGATCTACT[G/T]TCAAGATGGCTCATC | 23603 |
rs568291860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108705231 | CGCCTGTAATCCCCA[C/T]ACTTTGGGAGGCCGA | 23603 |
rs568303631 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733349 | GCTAAATTCTTAACA[C/T]TTTTCTGTAGAGATG | 23603 |
rs568320863 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685591 | TGGATAGGGAAAGAA[A/G]ATTTCCACTATGCCA | 23603 |
rs568337465 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708607 | GCTGGGATTACAGGC[A/G]CCTGCCACCACGCCC | 23603 |
rs568338384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718328 | AGCTGAAATCGCACT[A/G]CTGCACTCCAGCCTG | 23603 |
rs568425165 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712257 | TATTTAAATGACAAT[A/G]CCAACAGTAAAAAAT | 23603 |
rs568531211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108665428 | TTGAGTTACAATAAA[G/T]TGTATTGTAACCCAT | 23603 |
rs568533812 | in-del | -/TTTT | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647209 | AGCTTTTAAATCACG[-/TTTT]GTTTCTGCAAATTTG | 23603 |
rs568571067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108673961 | AAACAAAGCATGAAT[A/G]ACAGCACATCTGTTT | 23603 |
rs568571096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664083 | ATCAAGAACCCTACC[A/G]AAGACCAGATATTAA | 23603 |
rs568712477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680260 | CACAGTCTCTGGAGA[C/G]GTTTTCTTCTGGGAA | 23603 |
rs568748589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688507 | CTACATATTACAAAA[G/T]ATCATTCAGAATGAC | 23603 |
rs568827664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683067 | CTGAAAATTAATGCA[C/T]TGAGTTGCTACCTTG | 23603 |
rs568890456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108720121 | AGCCTGGGAGGGCGA[C/T]GCTGCATTGAGCCTC | 23603 |
rs568891421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108721233 | ATTTTACTCTAACAT[A/G]TTGTATAAATGCATA | 23603 |
rs568917638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667669 | CGGCGTTCAAGGCCA[A/G]CCTGTGCAACATAGA | 23603 |
rs568953805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108675826 | GGAAGAACATAATGC[A/G]AACAATATAGTCTAG | 23603 |
rs568956460 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651261 | ATAAACACAGTGTTA[C/T]ACAAATGTTTGGTAC | 23603 |
rs568993753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108684105 | ACATACCTAACAAAA[C/T]CAACAACCAAACAGA | 23603 |
rs569026285 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644932 | AACACAGTGCTTGAC[C/T]GGCTTGGAGACCTCA | 23603 |
rs569041852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108705244 | CACACTTTGGGAGGC[C/T]GAGGAAGGCAGATCA | 23603 |
rs569054483 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652300 | ATTTGTTAACATCAA[A/G]TCCCCTCTTGGGCAT | 23603 |
rs569062770 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689110 | GAGGCTGAGGTGGGA[C/G]AATCACTTGAACCCG | 23603 |
rs569093425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697856 | AGACTCACTCATATT[A/G]TGTAAACAATCAAAT | 23603 |
rs569170903 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661687 | AGAGGGAACACAGGG[C/G]TTCTGGCTCCCAACA | 23603 |
rs569201349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108674534 | GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA | 23603 |
rs569203159 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108688194 | GAGATTACAGGTGTG[A/G]GCCACCGTGCCCAGC | 23603 |
rs569206764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689962 | CAGAGTTCAAAGGAG[A/T]CAAAAGCGTATCTAT | 23603 |
rs569259262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108666657 | TCCTCTTGTGTGTAA[C/T]ATGGGATGCTGGCCT | 23603 |
rs569355843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108657067 | AAAATTAAAAAAAAT[A/T]AAAAAAATAAAAAAT | 23603 |
rs569407205 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108688642 | CTGGGCACGGTGGCT[C/G]ACACCTGTAATCCCA | 23603 |
rs569448647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695342 | GGCTAGCCCTATTCA[A/G]TGTTGGAGGCCACCT | 23603 |
rs569487592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108727363 | TGGGATTCTAGAAGT[A/G]GAAAGGCGATGAAGT | 23603 |
rs569555857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680913 | GTTGCTTAAGCTGAT[G/T]GTACTGGGATCACAG | 23603 |
rs569559474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108662681 | GGAATGGGAATGAAG[A/T]CACTTAGCTAAGTCT | 23603 |
rs569608532 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703211 | CAAGCAAGTGTTTCA[A/G]AAGTAAGCTAATGTA | 23603 |
rs569621211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663326 | GGTAATTCCACTCCT[A/C]GGGATATACCCAAGA | 23603 |
rs569643295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710918 | ACAAGTAAAAATAAG[A/G]TCTACCTCTATGGTT | 23603 |
rs569652025 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725833 | TTTATTTTTTTGAGA[A/C]GGATTCTTTCTCTGC | 23603 |
rs569726295 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712627 | ATATATAAGCCTACA[C/T]AGAATACACATTCAC | 23603 |
rs569850375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717331 | AACCCGGATCACAGA[C/G]GGCTTTCTAGGCCAT | 23603 |
rs569881066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725918 | TAGGCTCCCTGCAGC[C/T]TCTGCCTCCCAGGTT | 23603 |
rs569900056 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715414 | ATAAGGACTTCGAAA[C/T]CATCTCTAGCTCTTC | 23603 |
rs569938671 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717124 | AGCAGTCAGAGAAGC[G/T]ACACTTAAGCTGAAA | 23603 |
rs569943098 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732215 | CACCACCTCCCTTGA[G/T]GACTGCCGACGTTCC | 23603 |
rs570012921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718000 | AGGCGGGTGGATCAC[C/T]TGAGGTAAGGAGTTC | 23603 |
rs570025984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687193 | AAAATGTAAGCATCA[C/G]TAAAAATATAACTTT | 23603 |
rs570031630 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659677 | TGTTTAGGGCACTCA[A/G]CAAAAACTCTGGGTG | 23603 |
rs570033466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108671235 | CAGCTACTCGGAAGG[C/T]TGAGGTGGGAGGATT | 23603 |
rs570062331 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729781 | CTTCAGTTTTACAGG[C/G]AATGCAGAAAGTGAA | 23603 |
rs570108194 | in-del | -/TCAT | 0.00438332 | 0.0466095 | intron-variant | CORO1C | GRCh38.p7 | 12:108697992 | TGATAACATGGAAGA[-/TCAT]TCATTCTATTTTCTA | 23603 |
rs570114008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679357 | TAAAATGCTTAATGT[C/T]GGTCATAAATAGCTA | 23603 |
rs570123159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108700486 | GAAGGAGGAGGGCTT[C/G]GAACCCTACTGAAGT | 23603 |
rs570152491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108650445 | TTGGCCTCCCAAAGT[G/T]TTGGGATTACAGGGT | 23603 |
rs570167124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708528 | GTGCAATGGCTCAAA[C/T]TCGGCTCACTGCAAC | 23603 |
rs570178535 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108687666 | GGTGTGTGCCTATAG[C/T]CCCAGCTACTCAGGA | 23603 |
rs570179194 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686228 | CCAAAGAATCCATGT[A/C]TAATTAGCTAGATTG | 23603 |
rs570210514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108681039 | TTGTTCTTGTCTCAC[A/G]TTGCCTAGGCTGGAA | 23603 |
rs570360413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693827 | CTTCTGTTTCATCTT[C/T]AGCTCCTACGCAGAG | 23603 |
rs570365320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108649453 | GAGGTGGTTGAACAT[A/G]TAAGTATAAATATGA | 23603 |
rs570429101 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108657076 | AAAAATTAAAAAAAT[A/T]AAAAATATATAGTCA | 23603 |
rs570438435 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718498 | AGTGAGCAGAGATCA[C/T]GCCACTGTACTCCAG | 23603 |
rs570533175 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733298 | CACCTCAGCCTCCCA[C/G]GTAGCTGAGACTACA | 23603 |
rs570628091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108711100 | AGGCACAGTGGTTCA[C/T]AGTTGTACTCCCAGC | 23603 |
rs570646456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108695430 | TAGCCACCCAGTTTG[C/T]ATCCTCTATCCAAGT | 23603 |
rs570739366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108725995 | GCGCGTGCCACCACA[C/T]CCGGCTAATTTTTGT | 23603 |
rs570751364 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704394 | AGAGAATTGCTTGAA[C/G]CTGGTAGGCGGAGGC | 23603 |
rs570788224 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703279 | CTTCATAAATAAAAC[A/G]TTCTTACAAATTCAT | 23603 |
rs570809153 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682431 | CTTTAAGGTGAAATG[A/C]ACTATTAGCGATTAA | 23603 |
rs570812175 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685955 | CTAAGTATCTTCTTA[C/T]TCATAATGAAATCAA | 23603 |
rs570885355 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657165 | CAACGAGGATAAGAA[C/T]TTCACATCCAATCTA | 23603 |
rs570886735 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108711637 | GTGAACCGAGATCGC[A/G]TCACTGCACTCCAGC | 23603 |
rs570892322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716515 | AAGCGGAGATTAAAT[A/G]GATTAAATGAACATG | 23603 |
rs570892423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708627 | CCACCACGCCCAGCT[A/G]ATTTCTGTATTTTTA | 23603 |
rs570916760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715807 | ACCGCAAAACTTTTA[C/T]AGACATGAGTGACCT | 23603 |
rs570970270 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712469 | ATCCCAGCTACTCAG[A/G]AGGCTGAGGCACGAG | 23603 |
rs570981859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680034 | AGTTCTTCTAGTACA[A/C]TAATTTACTCCATCA | 23603 |
rs570995684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702606 | GTGGAAATGGAACAT[A/G]GTTCAACATCGACAA | 23603 |
rs571031390 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108664125 | GTTTATGAAAAAGCT[-/AA]AGTTTAAAATCATTA | 23603 |
rs571036715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108648543 | ACGCCCTGGACCACA[A/G]GGGCTTTCTAGAGGA | 23603 |
rs571159933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687769 | CAGCCTGGGTGACAG[C/T]GAGACTCTGTCTCAA | 23603 |
rs571266789 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | CORO1C | GRCh38.p7 | 12:108671033 | TCTAAAAAAAAAGAA[A/T]AAAAAAAAAAGGTTT | 23603 |
rs571349578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654066 | CCCCAATACCCCAGC[C/T]CAACCTCTGCTTCAG | 23603 |
rs571406296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108685046 | ATTTTTTCCAATCTG[A/G]GCTAAGAAGCGCTTT | 23603 |
rs571439523 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730809 | GCCCCGCCTGACCCC[C/T]AACCGAGATCTGCAG | 23603 |
rs571441744 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696462 | CAGAAACACTGGTGT[A/G]TATGAGCCCTCCATG | 23603 |
rs571495254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724070 | TTTTCAAGTTTCCTA[A/C]AAATGCATCTAAAAA | 23603 |
rs571519877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699439 | TTCCATTTCTTTGAA[G/T]GAAAAAAAAAGTCTT | 23603 |
rs571616080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660253 | GGTCAGGAGTTGGAG[A/T]CCAGCCTGACCAACA | 23603 |
rs571658664 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645901 | CCAAGCATGCACTAT[A/G]AGAAACTGGAAACGG | 23603 |
rs571677904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707383 | CCAGAAGTAAACTCA[C/T]ACATCTTTGGTCAAC | 23603 |
rs571765063 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722032 | CTGATTCCAGGTATC[A/C]GGACTAGCCTCCTTA | 23603 |
rs571803129 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108662992 | CCAAAGGACAAATAA[A/C]CCAATTGAAAAATAG | 23603 |
rs572014493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108706654 | GGGTGGAGCGCAGTG[C/G]TGCAATCTTGGCTCA | 23603 |
rs572063953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676977 | AGCCAAAAGCCCATG[A/G]GGAAAAGCGGGTAAA | 23603 |
rs572075294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108686606 | AATAAATTTTGATTC[A/G]TTGATTACTTACTAG | 23603 |
rs572099856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108687358 | CAGGTGTAGTGGTGC[A/G]CACCTGTAGTCCCAG | 23603 |
rs572118489 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647314 | ATGGCAGTGCCTCCC[C/T]TTCCGCCCTCCCTAG | 23603 |
rs572126842 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108663528 | GTACTGATACATGCT[A/G]CAACATGAGCAAACT | 23603 |
rs572160471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715161 | ATCCCTTGAGCCCAG[A/G]AGTCTGAGGCTGCAC | 23603 |
rs572160689 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691695 | GCTGACAGCCACAGC[A/G]CTCTGATGGCCATAT | 23603 |
rs572182431 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108715900 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 23603 |
rs572224303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108668740 | TTATGCAATCCCATT[G/T]TCCAAATTAGCCATT | 23603 |
rs572231616 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650982 | TTGTTTGTTTGAGAC[A/G]GAGTCTCGCTGTGTT | 23603 |
rs572245784 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690325 | CTACAGATTGAGTTA[C/T]CCTGTAAGGTAAGGT | 23603 |
rs572265197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108655362 | TCCCTCTCCCCTTCC[C/T]CCTCCCCCTCCCCCT | 23603 |
rs572272891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108654546 | CAGAAGTTTGAACTA[C/T]GCACATACAATACTC | 23603 |
rs572298371 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657905 | GGGTGGAGAAAACAC[-/T]TAACACAGGGCTGGG | 23603 |
rs572342975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108708751 | ACGGGCGTGAGCCAC[C/T]GTGCTCGGTCTATTT | 23603 |
rs572353179 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | CORO1C | GRCh38.p7 | 12:108655668 | ATTGCAAACGGAGTC[-/T]CGTTCACTCAGTGCT | 23603 |
rs572353220 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645397 | GAACCACATGCCCTA[A/C]GGTGTTTCACCACCA | 23603 |
rs572353324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653356 | AACATCTGCAGTAAA[A/C]TGGCTTTCAAGGAAA | 23603 |
rs572359388 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686544 | TTCTGGCATGAAATT[G/T]AAGTAGTTTAGCTGA | 23603 |
rs572392232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108722370 | TAAGAGAGAGATGAA[A/G]GAGGATGAAGAACAA | 23603 |
rs572470318 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730990 | ACCCAGTCCCCAGGC[C/G]TGGAGCCCCCGGGCT | 23603 |
rs572555214 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108700893 | CAACATCGTTATAAT[A/C/G]ATTTTTTCATCCATA | 23603 |
rs572690636 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108716553 | GACAGTGTTTCAAAG[A/G]AACATTAAGGAAGAG | 23603 |
rs572700995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728434 | AAAAGACCACATAGT[A/G]TATGATTCCATTTAC | 23603 |
rs572750931 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672929 | CATTGCTCCACCACC[C/T]GCTCTTCCTGTATTC | 23603 |
rs572761068 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108729210 | CAGAAGTGACAGATA[A/C]GTTAAACATAAAACT | 23603 |
rs572773664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108721368 | CACCCTCAGGCAGGA[C/T]CTCACTCCCAGTGTC | 23603 |
rs572788048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667849 | TCACATGTGAAAGCC[C/T]GGATATGGAAAAAGG | 23603 |
rs572810346 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108712813 | ATAATGAGGCACTGT[C/G]TCTAAGAAGGCTGAT | 23603 |
rs572852116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659884 | AATCAAGTAGCTACA[C/T]AGATTCAGAAACGGA | 23603 |
rs572906113 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704658 | TCTCTAAGCGGAGCT[G/T]GAAGGGCAGTGTGAG | 23603 |
rs573014864 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108706329 | CCACAGCTAACTCAA[C/T]ATTCAATGGCGAAAG | 23603 |
rs573070891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667202 | GAGTCTTGTCTTCAA[A/C]TTAATTCAGCACTGT | 23603 |
rs573187633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675241 | TTTTCCCTTAAAATA[A/C]ACCAGGACTTCCGAA | 23603 |
rs573205323 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701976 | CTCACTACCAAACCG[C/T]CTAGTGCTAAGTGGT | 23603 |
rs573249863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108690028 | TCTTATGACAGTATT[A/G]TTTATGTGGATACAT | 23603 |
rs573288048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697094 | CTAACTTATTTTACA[G/T]TCTCCCAGAATCTAA | 23603 |
rs573296446 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730202 | TGAATCCCACGTTTG[C/T]AACATGTAGAGCAAG | 23603 |
rs573300217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651037 | CATCTCGGCTCACTC[C/T]GCCTCCTGGGTTCAA | 23603 |
rs573340976 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108719532 | TCCTTGTCAAATTCT[C/T]AAGTCAAACGAATTC | 23603 |
rs573361979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681473 | AACAGAGAAAGGACA[C/G]ATTACCTACTGACAG | 23603 |
rs573407663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108718760 | TGCATCTTCTAAAGC[A/G]AAGGAAAAAACAAAA | 23603 |
rs573422174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664365 | CTGGATGAGTGTTTA[C/G]GGTTCAGCTCAGTTC | 23603 |
rs573485838 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670423 | CAAAATCACCCACAG[C/T]GGGCTCCCTTCCAGG | 23603 |
rs573491999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108721536 | AATTTAAAAGTAAAT[C/T]AAAACATTAAGCTTG | 23603 |
rs573505449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108657498 | AAACTCGGGCACAGA[G/T]CCAACCTCACCAACT | 23603 |
rs573552754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108722198 | GTACACCTCTAAAAG[C/G]GTTAAAGAACATGAG | 23603 |
rs573608514 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700013 | GGACATTTTCCCAAT[A/G]AGAGTTTTCCCAAGG | 23603 |
rs573612994 | snp | A/G | 0.431621 | 0.171796 | intron-variant | CORO1C | GRCh38.p7 | 12:108652848 | ACGCAATGCTGTTAT[A/G]CCAGTATGATGATAA | 23603 |
rs573671267 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696243 | ACAATACTCAAGGAA[G/T]GAAGGGAGAAAGAAA | 23603 |
rs573675041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108653589 | ACAAGAAAAAAAAGG[A/G]AACTATAAGGTTCCC | 23603 |
rs573708113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108697175 | AAATAGCTTTCAAAA[G/T]AAATTCATGGAAAAC | 23603 |
rs573721875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108660544 | CTCTGGGATGGACAA[C/T]TGAACCTTCCTCTGC | 23603 |
rs573765328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108728581 | ACTGTACACTTTAAA[C/T]GGGTGAACTGTACAG | 23603 |
rs573782183 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108694107 | GCCAACACAGTGAAA[-/CT]CTGTCTCTACTAAAA | 23603 |
rs573830787 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO1C | GRCh38.p7 | 12:108698875 | TCTATGCCACATTGA[C/T]GCTAAGAGCTAAATA | 23603 |
rs573833534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667489 | TATCCCTACTTCCTC[A/T]TTTTTATTTTATTTT | 23603 |
rs573839598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108714142 | ACACCTATAATCCCA[A/G]CACTTTGGGAGGCCG | 23603 |
rs573932081 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727566 | AGAGGATTTGAACAG[C/G]TGAATGGCATGTTCC | 23603 |
rs573964779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108659933 | ATGTCAACTCATTCA[C/T]CATCTCAGCTCACCA | 23603 |
rs574002109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108667975 | TTTTATTTTTCAAAT[A/G]CTGCTTTCCAGACAC | 23603 |
rs574042903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108696610 | TGCTCTTGAGACAAG[A/G]CAGCTTGTGCAGTTG | 23603 |
rs574050999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673515 | GTCTGGATAAGATCA[C/T]TGATGAAGGTGGCTA | 23603 |
rs574074922 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108675270 | AAAGAAATGGCTTGG[C/G]CAGGGATGTCCAAAG | 23603 |
rs574138570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712704 | TATAAAAATTTGGCC[A/G]GGCACGTTGGCTCAC | 23603 |
rs574175114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108666057 | AAATTAGCTTCCTGC[C/T]AACCAAGCTTGGTCC | 23603 |
rs574209670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651754 | CTTCAGTTATATGGG[C/T]AGGAAATGAGGTATT | 23603 |
rs574209960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658216 | TTTATTTATTTATTT[A/T]TGTATTTTTAGTAGA | 23603 |
rs574251737 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658780 | AATGACTCTCACTTT[C/T]TTGTCTTTGGAAGCT | 23603 |
rs574255972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658962 | AGAAGATTAGAAACA[C/T]CTATGTAACACACTC | 23603 |
rs574296506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651189 | CTTTTATTTGGAAGA[A/C]GTAAGTATCAATTCT | 23603 |
rs574306132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681332 | GGTTCAGTTAAATGC[A/G]TAAGTCTTTAGATTT | 23603 |
rs574325167 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728179 | AGAGTTACCATACAA[C/T]CCATCGATTACATTC | 23603 |
rs574512716 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108688201 | CAGGTGTGAGCCACC[A/G]TGCCCAGCCCAGTAT | 23603 |
rs574513547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726848 | CTGTGCGCCAGTCAT[C/T]ACTGTTCATCGGGGG | 23603 |
rs574656867 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CORO1C | GRCh38.p7 | 12:108665864 | AGGACATTCACCTAA[C/T]CTTTCCAGGACTTAA | 23603 |
rs574763393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108710597 | TTGAGACAGAGTCTC[A/G]CTCTGTCACCAGGCT | 23603 |
rs574775066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656292 | CGGGAGGGAGGTGGG[A/G]GCTCAGCCCCCGCCC | 23603 |
rs574877650 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679215 | TATCATTAGGGCCTA[A/G]AGAGCCTACTACATT | 23603 |
rs574897580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656591 | CATGATGACGATGGC[A/G]GTTTTGTGGAATAGA | 23603 |
rs574931852 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO1C | GRCh38.p7 | 12:108678895 | GGGAGGCTGAGGCAG[A/G]TGGATCATGAGGTCA | 23603 |
rs574979541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659014 | GAATACACATATGTA[A/T]ATGCAGAGAGAGAGA | 23603 |
rs575034537 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702838 | TCTCTCCAATGCTGG[A/G]GGCATGTAGCCGGGC | 23603 |
rs575045046 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732557 | TTAATAGCTAAAGTC[C/T]CTTTCTGAAACACCA | 23603 |
rs575068389 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703045 | GCGTGAGTTAGATAA[A/G]ACAGCTTCCATGAGG | 23603 |
rs575088076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108675197 | ATATATATATATACA[C/T]AATGCTACTGCATAC | 23603 |
rs575089211 | in-del | -/GC | 0.00676609 | 0.0577691 | intron-variant | CORO1C | GRCh38.p7 | 12:108661846 | GAAACACACACACGT[-/GC]GCACACACACACAAG | 23603 |
rs575162466 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108728351 | ACCATTAAAAAAAAA[A/T]AATGAAGTACTATAC | 23603 |
rs575173314 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687644 | ACAAAAATTAGCTGC[A/G]CTTGATGGTGTGTGC | 23603 |
rs575227415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108671346 | AGAAAGAAAAGGAGT[A/G]GGGGGAGGAAAAGAA | 23603 |
rs575257587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108711263 | CGGTCCCAGCTACTC[A/G]GGGAGCTGAGGTGGG | 23603 |
rs575293343 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108712304 | GAGGCCGGGCAGGGC[A/G]GCTCACACCTGTAAA | 23603 |
rs575331678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108719822 | ATTATGGTTCTTGCC[A/T]TATCTATCTTCATTG | 23603 |
rs575356398 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108696534 | CGAGTGTGGCTACTC[A/C/T]ACAAAGGAAAGGCTT | 23603 |
rs575367538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108712739 | GCAATCTCAGCATTT[C/T]GGGAGGCTGAGGTGG | 23603 |
rs575427083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108717553 | ACAAGTCACAGTCCC[A/G]GTAGAAACAGAGATG | 23603 |
rs575457032 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108647989 | AACCCTTGCCCTGTG[G/T]GTCCACTCCTTCTCT | 23603 |
rs575480004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689269 | GGAAATGTAACATTA[C/T]GTTAAAGTCGCACAA | 23603 |
rs575485870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108680597 | CTCAACCTCGGTTCC[C/T]CATCTATAAAACTAG | 23603 |
rs575491200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108718612 | ATAAAAATCTCCCTA[C/T]GTTTCTGGAATTTTC | 23603 |
rs575569697 | snp | G/T | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644727 | AATCAACTCATAATA[G/T]TAACAGTAGCGGCCA | 23603 |
rs575571754 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702912 | TTAGCCCAGCTGTTA[C/T]TGCCAGACTTTCCCA | 23603 |
rs575576894 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703755 | CTCTCCCCAGCAGAA[G/T]CCAGGAGAGGCCTGA | 23603 |
rs575578071 | snp | A/G | 1.6517e-05 | 0.00287372 | intron-variant | CORO1C | GRCh38.p7 | 12:108648934 | ACATTTGTTTAAAAT[A/G]TGGATTGTCTAGAAA | 23603 |
rs575601210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687414 | ATCACCTGAGCCCAG[A/G]AGGTCAAGGCTGCAG | 23603 |
rs575604344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108682332 | AGCTACACATATTTT[A/T]AAAAAATAATGGCAC | 23603 |
rs575604446 | in-del | -/A | 0.498568 | 0.0267188 | intron-variant | CORO1C | GRCh38.p7 | 12:108674553 | ACTCCGTCTCAATTT[-/A]AAAAAAAAAAAAAAA | 23603 |
rs575606519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108650966 | TTTGGTTTGTTTGTT[C/T]TTGTTTGTTTGAGAC | 23603 |
rs575644091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108693961 | TCATGCACAAAGCAC[A/C]CCCCTGGAGAGATCA | 23603 |
rs575647141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108681419 | ATATCCTAGTGCAAT[C/T]TAGAACACCTAAAAC | 23603 |
rs575763669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108688027 | CTCCCAGGTACAGGC[A/G]ATTCTCCCGCCTCAG | 23603 |
rs575865200 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691511 | TTCTGCTGGCAGCAA[C/T]TGTCAGCCTGCTTAG | 23603 |
rs575869489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108673115 | AGTGAGGAAGCCATG[C/T]TGAAAGCTGAAACAG | 23603 |
rs575878456 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108730678 | ATCCGACAGCCTTCC[G/T]GCTTCGTTCCTCCCC | 23603 |
rs575986695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669497 | TTATATGGAAGGCAA[C/T]TGGGGCTGAGAGCGT | 23603 |
rs575991381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108664207 | TGAGGAACTAGCTCA[C/T]GAAAAATTTAAGAAC | 23603 |
rs575999823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108656832 | AGATGTGCTTTGTTG[A/T]ACAGATGCTTGAAGG | 23603 |
rs576002460 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699604 | AAATGTCAAGTTTCC[A/G]AATGCCCCTTGCTCT | 23603 |
rs576027777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108663626 | GTGAAATGTCCAGAA[C/T]AGGCAAATCCGTAAA | 23603 |
rs576053211 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651326 | TGTTGTTTGAAATGG[-/C]CAGTGGTCACTGAGT | 23603 |
rs576080657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108679647 | GAGCAGGCTTCTTAG[C/T]AATTTTTCAAGAACA | 23603 |
rs576110387 | snp | C/T | 0.000148528 | 0.00861639 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662080 | AAGCCACGATGCCGA[C/T]TCTCTTTGAGTGGCC | 23603 |
rs576149219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108661554 | TTTCCTTTTGTTTAT[A/G]TATGTTCTCTACAGT | 23603 |
rs576169738 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108709588 | TTTTAACCTTTAAAT[G/T]AAGATGGCATATCAC | 23603 |
rs576177741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108708978 | CTGGTCTCTAACTAA[C/T]TGCTGGCTTTAAGGA | 23603 |
rs576251538 | in-del | -/GAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690240 | GGAATAAAACATTCT[-/GAG]GAGGCTTTACTTTAA | 23603 |
rs576274135 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716221 | TTCTTATCAACAACT[A/G]GTAAAAAACACACTG | 23603 |
rs576276914 | snp | A/C/G | 3.31089e-05 | 0.00406861 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647386 | CCATTTTTTCTGTAG[A/C/G]GGTGGGGGTGGGACC | 23603 |
rs576311580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108687444 | GTGAACTATGATCGC[A/G]CCACTGCACTCCAGC | 23603 |
rs576314997 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | CORO1C | GRCh38.p7 | 12:108676130 | ACACCTGAGTGATTA[A/C]CACTACAAAGAAAGG | 23603 |
rs576345072 | snp | A/G | 1.70557e-05 | 0.0029202 | intron-variant | CORO1C | GRCh38.p7 | 12:108678225 | GCTTTTGAAAGCAGT[A/G]GGTGAGTCTCACTGG | 23603 |
rs576374333 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712726 | TTGGCTCACGCCTGC[A/T]ATCTCAGCATTTTGG | 23603 |
rs576412135 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731649 | GCCCACTTCCGGAGG[C/G]GAAGCCCGCTTCCCA | 23603 |
rs576421343 | in-del | -/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657603 | GATACTATGTGATCT[-/G]GGTCAAGGTCCCTCT | 23603 |
rs576453380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658182 | TTGTTGCTTTTCGCC[A/C]TGCGCATTTATTTAT | 23603 |
rs576496565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724255 | GCAAAAGAGCATGAC[C/G]AAAGGCTAAGCAAAT | 23603 |
rs576499662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670264 | ACAGCAAGGGGACAC[C/T]TGACAGACCTGAGGG | 23603 |
rs576506042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108673267 | TTTTAGTGGTCTGGA[C/T]AGAAATACAAACCAG | 23603 |
rs576542877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108672539 | TATCCCTAAGACCCT[A/G]CATTCTCTGTGTGAA | 23603 |
rs576543125 | snp | C/T | | | intron-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108653086 | GGAGATATACATATA[C/T]GTAAGAAAGAAGAAG | 23603 |
rs576544805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108680422 | AAAAAAGGAAATTCC[A/G]ATGAACACCATATCA | 23603 |
rs576550426 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CORO1C | GRCh38.p7 | 12:108684459 | CTCCCATATTTTGTA[A/C]AAGAGGAATATTTAT | 23603 |
rs576563970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108715960 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATG | 23603 |
rs576574007 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | CORO1C | GRCh38.p7 | 12:108686919 | CTGGCACAAGGGAGA[-/G]GTGTAATGGCACAAT | 23603 |
rs576590304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108699601 | GTAAAATGTCAAGTT[C/T]CCAAATGCCCCTTGC | 23603 |
rs576595573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108656025 | GGAGCGCCTCTGCCC[A/G]GCCGGGACCCCGTCT | 23603 |
rs576626216 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108731104 | AGCCTCGTCCCACCT[C/T]GGCCCGCGGCTCCGC | 23603 |
rs576629432 | in-del | -/GGGA | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108656372 | CCAGCCGCCCCGTCC[-/GGGA]GGGAGGTGGGGGGGC | 23603 |
rs576654549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108656564 | GTACCCAACAGCTCA[C/T]TGAGAACGGGCCATG | 23603 |
rs576661218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108677849 | CATGGTGAAACCTCG[C/T]CTCTATTAAAAATAC | 23603 |
rs576698053 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CORO1C | GRCh38.p7 | 12:108685319 | TCAACATTTTCTCTG[C/G]AACCTGAATGTCACT | 23603 |
rs576742412 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648830 | TGTGTCAGGATACAG[A/G]TCATCTTGGAAAAGG | 23603 |
rs576758608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686853 | ACAGCCTGCCCAGAG[C/G]CAAGCAACATGAGCC | 23603 |
rs576761092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108726227 | TCGAGATCATCCTGG[C/G]TAACACAGTGAAATC | 23603 |
rs576777363 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108689596 | TCTGCAGTCCTCTAT[A/C/G]CCTATTATCCAGACT | 23603 |
rs576915312 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108656129 | GTCTGAGAAGTGAGG[A/G]GCCCCTCCACCCGGC | 23603 |
rs576930201 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108694020 | AAGAACCTAGCCGGG[A/T]GTGGTGGCTCACGCC | 23603 |
rs577079183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702793 | TTTGCCAGAGTCTCT[C/T]ACCCTTCCAACGCAT | 23603 |
rs577117160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108710521 | GATAACTAATATTCA[C/T]AATACTTAACATCTA | 23603 |
rs577117324 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108702036 | AAAGCAGCCTAACGG[G/T]TAAGAGCCAGGTCTG | 23603 |
rs577148387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716953 | GAGAGACACAACTGT[A/G]AGCAAGCAGACCTGG | 23603 |
rs577168509 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668370 | AAATGGAATTAAGAC[A/G]AAGCCCTCCCTGCTG | 23603 |
rs577184255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108716020 | CCTGTAATCCCAGCT[A/G]CTCGGGAGGCTGAGG | 23603 |
rs577256704 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO1C | GRCh38.p7 | 12:108697805 | ACACAGCAGGTACTC[C/T]GCTTACAGACAATCA | 23603 |
rs577343713 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677541 | CACCTGTGACATATC[C/T]CATTTTATCTGCATA | 23603 |
rs577384771 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679840 | TAAGCTTCACCTCAT[C/T]CGTCATCTGTAAAAT | 23603 |
rs577397124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108714533 | CCTGTATTCCCAGCA[C/T]TTTGGGAGGCTGAGC | 23603 |
rs577426132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108724302 | GTCAAAGACTACAAA[A/G]GGAAAGCCATGTCAG | 23603 |
rs577467267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108670501 | AGGATAGCAGTAAGA[A/G]GGATAAAAGCATAAG | 23603 |
rs577485235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108686441 | TCTAAAGCTTAGAGA[C/T]AGAAAAACTTCACTT | 23603 |
rs577533449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108699768 | TGAACAGAAATAAAA[A/G]TATCTAAATAAAAAA | 23603 |
rs577558776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108707122 | TTCCCCAAACTAAGA[C/T]ATAGATTTAATGCAA | 23603 |
rs577558807 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108715048 | CAAAACAGTAACACA[A/T]AATGAACCTGAAGAC | 23603 |
rs577564933 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727351 | CCAAAGGACAAGTGG[G/T]ATTCTAGAAGTAGAA | 23603 |
rs577588739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108683643 | AGATGAAATACACAA[C/T]CTCACAGAAGTAAAA | 23603 |
rs577609586 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719149 | ATCTTTAATTCTCTA[C/T]GCTAAATTAATTGGA | 23603 |
rs577624244 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723877 | ATGCAATGCAAGGGC[A/T]CCTTTGCAATAATAA | 23603 |
rs577646346 | snp | C/T | 1.66585e-05 | 0.00288599 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678277 | GGGAGCTTACCATGA[C/T]CGTGCAGTCCTCTGA | 23603 |
rs577679301 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646679 | AAGAAGAAATACGAC[A/G]TGAGCTTTTTTGATC | 23603 |
rs577724707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108668690 | GACTATCATTTTGCA[A/G]TATCTTTCCAACTCC | 23603 |
rs577741690 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108654510 | TCTATCCCAATTAAG[A/C/T]GAGCCATTTTCCTAG | 23603 |
rs577748936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108723219 | AACAGAGATGACAGC[A/G]CACTTTCACGTGTGT | 23603 |
rs577758512 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CORO1C | GRCh38.p7 | 12:108701010 | CTTAACTTCAATTAC[A/C]TCAGAGTCTAATGGT | 23603 |
rs577784975 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667266 | AAGATATCATTATGT[A/G]TGAAAGCTCTGGTTT | 23603 |
rs577800016 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697186 | AAAAGAAATTCATGG[A/G]AAACCATGTTTTCAA | 23603 |
rs577802556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108685477 | ACAACCTTTAAGATG[C/T]GGGAATCTTATCACC | 23603 |
rs577844550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108651881 | AAAAGTGAGATGTGC[C/T]GGGTGTGGTGGTGGG | 23603 |
rs577891508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108669338 | TACTGTATTTTTCTA[C/T]GAAATGTCTATTAAA | 23603 |
rs577893111 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | CORO1C | GRCh38.p7 | 12:108694396 | AAGTACTGTGTTAAA[-/T]TTTCACAAACATTTA | 23603 |
rs577987496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108661287 | GAAATAGGGGACTTA[C/T]CAAGTAAAATGAGGT | 23603 |
rs577990614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108653760 | CAAGCCCAGAGCCCT[A/T]GCACTGAACCCCAGG | 23603 |
rs578002269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730223 | GTAGAGCAAGCACTT[C/T]AGACACCACAAAACA | 23603 |
rs578016580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108660634 | AAATATGCAGAACAC[A/G]ACAATCACCCATTCT | 23603 |
rs578032928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO1C | GRCh38.p7 | 12:108676834 | TCTCTTAACAAAATG[C/T]GTCCATAGCCATTAA | 23603 |
rs578058012 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | CORO1C | GRCh38.p7 | 12:108668377 | ATTAAGACGAAGCCC[-/T]CCCTGCTGAATGCCT | 23603 |
rs578083919 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722829 | ATGATATGTTATTTG[C/T]TCTACTTGATAAAAG | 23603 |
rs578111673 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CORO1C | GRCh38.p7 | 12:108697326 | TATAACCAGAAACAA[A/C]AAAGGGAAAACATTC | 23603 |
rs745311450 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697480 | TATCTTGATTTCAAA[C/G]ATAACTTCATATTAT | 23603 |
rs745337401 | snp | C/T | 4.96339e-05 | 0.00498142 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658926 | TATCACAGCCTAAAA[C/T]AGGCAAAACCATCAG | 23603 |
rs745415066 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704183 | ATACTAAACTACCTT[-/A]AAAAGTGATTTCCAC | 23603 |
rs745460880 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663035 | AATAGACATTTCAAG[G/T]AAGACATATAAATGG | 23603 |
rs745485322 | in-del | -/AAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716854 | CAACTATGAATGTTG[-/AAT]AATAGGTCCTTAATC | 23603 |
rs745500260 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729660 | TACTATTATGCTTCA[C/T]AGCCAAACATTATGA | 23603 |
rs745506701 | snp | C/G | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648621 | ACACTGGCCGTGTCT[C/G]TGGTTTTCTTGGGGA | 23603 |
rs745550058 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663977 | AAGGAATGAAAGACT[C/T]TATGTTTAACAATGA | 23603 |
rs745571301 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687859 | TAGCTGTAAGGGCAC[C/T]TCCTATCAATCTTAC | 23603 |
rs745587708 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716917 | CGGCTTTGACCATGC[A/G]CCTAGCACCATGCTA | 23603 |
rs745597138 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652340 | CCCTCTCTGAGGCTC[C/T]TTGCTGCTGAATGTG | 23603 |
rs745600644 | in-del | -/AA/AAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712913 | AGATCATGTCTCTTT[-/AA/AAA]AAAAAAAAAAAAAAA | 23603 |
rs745650940 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673193 | AAAAGAAAAGTTCAG[A/G]AAATTAAAAGTGCTA | 23603 |
rs745728099 | snp | A/G | 8.27e-05 | 0.00642986 | intron-variant | CORO1C | GRCh38.p7 | 12:108649029 | GAAGAATCTTCAGAG[A/G]GGAAATAAAGGCAAA | 23603 |
rs745789347 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705641 | GGCCAGTATTATCCT[C/G]ATACCAAAACCAAAC | 23603 |
rs745801590 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669511 | ACTGGGGCTGAGAGC[A/G]TTTAAGCGAAGCGAC | 23603 |
rs745893313 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693582 | ATGTAGGATTTTCTA[C/T]CAAAAAGCTATCCTT | 23603 |
rs745911509 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680349 | TTCTTCACATTCCTC[A/C]ACTTTCCCTTGCAAC | 23603 |
rs745933168 | in-del | -/T | 3.62365e-05 | 0.0042564 | intron-variant | CORO1C | GRCh38.p7 | 12:108654453 | ATGTGTATGTATACA[-/T]TTTTTTTAAAAATAA | 23603 |
rs745934008 | in-del | -/AAT | | | cds-indel, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646852 | TGAATGTTTATACAA[-/AAT]AATATCTTATCTTCA | 23603 |
rs746017615 | snp | A/G | 1.69077e-05 | 0.00290751 | intron-variant | CORO1C | GRCh38.p7 | 12:108657257 | ACCTGCTCAGAACAG[A/G]GAGAAAGCTCAAGTG | 23603 |
rs746036881 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650023 | AGACAACCTGGCAGA[C/T]ACACTGCTCTAACGC | 23603 |
rs746059479 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712405 | ATGGTGAAACTCCAT[C/T]TCTAGTAAAATACAA | 23603 |
rs746156983 | in-del | -/TTTTTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652055 | GATTTTTTTCTTTTC[-/TTTTTT]TTTTTTTTTTTTTTT | 23603 |
rs746157341 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724341 | TGTTAAATAAAAAAT[C/T]CACACTATACTATAA | 23603 |
rs746170862 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722902 | AAAGATCAAACTAGC[A/C]GTCTTAGGGAGAAAA | 23603 |
rs746178396 | snp | A/G | 6.58979e-05 | 0.00573974 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701269 | TGGTCATTTTTCACC[A/G]CTTGCCCAAATACAT | 23603 |
rs746180650 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652054 | AGATTTTTTTCTTTT[-/C]CTTTTTTTTTTTTTT | 23603 |
rs746187245 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702008 | CACAGTGAGAAACAG[C/G]AAAAGTCAGCCTAAA | 23603 |
rs746245362 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702508 | AGATTTCCTAGACTG[C/T]ACCCAATGTAATTTT | 23603 |
rs746265404 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713354 | TGGTTCAATTGATTA[C/T]AACACCAGGAATGGT | 23603 |
rs746275074 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670049 | GGAAGATGAGAGAAT[-/C]CTCAGTGGCAGCATT | 23603 |
rs746302865 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667136 | GCTGTTAATATGACC[A/T]CTATGACGCCATATA | 23603 |
rs746313291 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705301 | TTAGGCAACATGGTG[A/G]AACCCAGTCTCTACT | 23603 |
rs746337740 | in-del | -/CAAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660451 | AGCGAAACTCCATCT[-/CAAA]AAAAAAAAAAAAAAA | 23603 |
rs746361122 | snp | A/G | 0.000332502 | 0.0128895 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702852 | GGGGCATGTAGCCGG[A/G]CTGAAGTAAGAGACC | 23603 |
rs746420269 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668228 | ATGTAGGGCATCAGG[A/G]CATTCCCAAATGAAC | 23603 |
rs746451253 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708617 | CAGGCGCCTGCCACC[A/G]CGCCCAGCTAATTTC | 23603 |
rs746453716 | snp | C/T | 0.000115309 | 0.00759218 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648755 | CAAGGAGATGAGGAT[C/T]GGGTCTGCATTCTTG | 23603 |
rs746463210 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721366 | CACACCCTCAGGCAG[C/G]ATCTCACTCCCAGTG | 23603 |
rs746550331 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690584 | CAGAAAGCAAAAACA[C/T]GGAAAAGTTAACATT | 23603 |
rs746564481 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648644 | CTTGGGGATGCTGAT[C/T]AGGTCGCACTTCTTG | 23603 |
rs746610029 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675457 | TGAACCCATCAAATA[C/T]GTTCAAATCCATGAC | 23603 |
rs746623685 | in-del | -/AT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650942 | AAAAAAAAAAATCAC[-/AT]AGAGAGTTTTGGTTT | 23603 |
rs746654064 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709435 | CTCCCATTTCAGCAC[A/G]GTATTTCTGCAGTTT | 23603 |
rs746721724 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674554 | CTCCGTCTCAATTTA[-/A]AAAAAAAAAAAAAAA | 23603 |
rs746774876 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670092 | TTCCGAAGTCCCTCC[A/G]TAAAAAGACAGAGCT | 23603 |
rs746775572 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720207 | TCATACAGACACACA[C/T]ACACGCACACACAAA | 23603 |
rs746814144 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728307 | GGATAAACAAAATAC[A/G]GCATATCCAAACAAT | 23603 |
rs746847918 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697315 | ACCTGCCTGTCTATA[A/G]CCAGAAACAAAAAAG | 23603 |
rs746900410 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646466 | ACGTCTTCCTGTCCT[A/G]GGCACCCTTGTCAAG | 23603 |
rs746922765 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715206 | ACCACTGAACTTGAT[A/G]CCAAAAGACAAAGCG | 23603 |
rs746923531 | snp | C/G | 1.66582e-05 | 0.00288597 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658948 | AACCATCAGAGATTA[C/G]AAGATTAGAAACACC | 23603 |
rs746928459 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663523 | ATGAAGTACTGATAC[A/G]TGCTACAACATGAGC | 23603 |
rs746944357 | snp | C/T | | | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647418 | TCAGGCTGCTATCTT[C/T]GCCATCTGCTGTTCT | 23603 |
rs746953184 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694616 | AATTGAAGTTAAGTA[C/T]GAGATAATGACTATG | 23603 |
rs746953646 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686504 | ATAAATCACCTCTGT[G/T]GCTTAATCTAGAATA | 23603 |
rs747008469 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729363 | ATCATGAAAAAGTCA[A/G]TATTGTGTGCAGTTA | 23603 |
rs747144557 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704290 | CATCCTGGCCAACAT[G/T]GTGAAACCCCATCTC | 23603 |
rs747162545 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656374 | AGCCGCCCCGTCCGG[A/G]AGGGAGGTGGGGGGG | 23603 |
rs747170029 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654978 | CCCAAAGTGCTGGGA[C/T]TACAGGAATGGCCAC | 23603 |
rs747177416 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722685 | ACTGAGTTAGACTCT[C/G]GAACACAACCCAGTC | 23603 |
rs747192141 | snp | C/G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692666 | ATGGTATAGACCAAG[C/G/T]ACTTTCCAAACCTAA | 23603 |
rs747208725 | snp | A/T | 1.684e-05 | 0.00290167 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678378 | ACTGTAGGGTAAGAT[A/T]TGTCAATTCGACCAG | 23603 |
rs747229949 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679260 | TCTCTGCTATCCTCA[A/G]TCAACAGAAATGCCA | 23603 |
rs747335016 | snp | C/T | 0.000166597 | 0.00912529 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702906 | CGTTCCTTAGCCCAG[C/T]TGTTATTGCCAGACT | 23603 |
rs747353236 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727392 | GTAATAAATTCATCA[C/T]AAGATTTGAAAGCTG | 23603 |
rs747424130 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680126 | AGATACAGACGTGAA[C/T]AAGGCAGTCCTGTCC | 23603 |
rs747424189 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724254 | GGCAAAAGAGCATGA[C/T]GAAAGGCTAAGCAAA | 23603 |
rs747467134 | in-del | -/A | 1.65166e-05 | 0.00287368 | intron-variant | CORO1C | GRCh38.p7 | 12:108701333 | TCGTGTCTGCAAAGG[-/A]AGAGTGAGAATTATG | 23603 |
rs747508996 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700447 | AATCTCCCACCTTGG[A/G]GCAGGCTTTCTGGGA | 23603 |
rs747515987 | snp | G/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657350 | ATGCGGCTGAACCCA[G/T]TGGTGAAGACATTGC | 23603 |
rs747522010 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731729 | CAGGCGGTGCCCAAG[C/T]GCACGCCCCGCTCTC | 23603 |
rs747553141 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666180 | TCTCAAAATAAAACA[C/T]GCAGATGTGTAGAGC | 23603 |
rs747605922 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701489 | TTTAGCAGCACATAC[C/T]CGGAGACAACTGCAA | 23603 |
rs747636918 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661493 | GAAACATCAAAAAAG[C/T]AATAATGATCTTCTC | 23603 |
rs747687029 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675192 | AATGTATATATATAT[A/G]TACATAATGCTACTG | 23603 |
rs747704915 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701563 | TTCAAGATCCAGAAA[C/G]AGCTCATCAGTTTTA | 23603 |
rs747705042 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688072 | GGGATTACAGGCACA[C/T]GCCACCACGTCCAGC | 23603 |
rs747712315 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | CORO1C | GRCh38.p7 | 12:108648859 | GGTCAGACTACAAGA[C/G]ACATTTGGCACCCGT | 23603 |
rs747759139 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663383 | AACTTGTACAAGAAT[A/G]TTCATAGAAGCATTA | 23603 |
rs747777451 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719457 | AAATGAACTCCTAAG[C/T]GATTAGATCATTTTA | 23603 |
rs747783839 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707307 | ACAAAGCAACAGTAA[C/T]CAAGACTGTGTGGTA | 23603 |
rs748003521 | snp | C/T | 1.66576e-05 | 0.00288592 | intron-variant | CORO1C | GRCh38.p7 | 12:108662199 | CCACATGAAAGCTAT[C/T]GCCTTTCATTATCAC | 23603 |
rs748045938 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648784 | TGCCTTCGAACCACT[C/G]TTCTGCCTCCAGCGC | 23603 |
rs748051986 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708393 | ACAAAAATCGACATA[-/C]CTAATTTATATGAAA | 23603 |
rs748057429 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660963 | TTAAAAACTGAACTG[C/T]CCCTCCTCCTTTTTA | 23603 |
rs748064949 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662687 | GGAATGAAGACACTT[A/G]GCTAAGTCTGTGGTT | 23603 |
rs748101459 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690884 | CATTCAATATCAAAT[C/G]AGAAAATAGAGAAAC | 23603 |
rs748130199 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | CORO1C | GRCh38.p7 | 12:108701120 | GGAAGATCAAATTAC[C/T]TACCTTGTGCAGAGG | 23603 |
rs748200500 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703261 | CATGTCAGAGTTAAC[A/G]TCCTTCATAAATAAA | 23603 |
rs748268093 | snp | A/G | 1.7144e-05 | 0.00292775 | intron-variant | CORO1C | GRCh38.p7 | 12:108678401 | TCGACCAGTCTGAAA[A/G]AAGAGAGAAACAAAC | 23603 |
rs748283648 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652373 | GAGGTAGTGGACGTA[C/T]GGGGATTCATCCGTG | 23603 |
rs748288525 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714313 | AGAATTGCTTGAACC[C/T]GGGAGGCAGATGTTG | 23603 |
rs748311144 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684941 | TACATCAGGGTCTTT[A/G]CATTCCTAGGCTCTG | 23603 |
rs748312122 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704249 | TTGGGAAGCTGAGAC[A/G]GATCACGAGGTCAGG | 23603 |
rs748327023 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668525 | CACCCGCCAAAAAAA[A/C]CTATATTAGGAAAAT | 23603 |
rs748360736 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690809 | AATAAAATTGAGCTA[C/G]AAAGCAAAAGCTGAA | 23603 |
rs748376685 | in-del | -/ATTAACGTTGTTTTCACCT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674115 | AAAATGTACAAGGAG[-/ATTAACGTTGTTTTCACCT]GCTAACATCAATTCT | 23603 |
rs748417022 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653643 | GCTACCCACAGTCTA[C/G]GTATGCTGAGCTCAT | 23603 |
rs748418631 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669590 | TTCTACTAAAACTAG[G/T]CCTTGTTATACTATC | 23603 |
rs748441004 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684334 | GGAACTCATAAACTG[C/T]TTACAGAACACCTTG | 23603 |
rs748455429 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722589 | ATTCCTTCAGTCTAG[A/G]CTGGGAACGTACCCA | 23603 |
rs748467091 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678984 | GTCGTGGTGGTGTGC[A/G]CCTGTAGTCCCAGCT | 23603 |
rs748535930 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664230 | TTAAGAACTTGTCAA[C/T]GAAAAATCATGTTCA | 23603 |
rs748629343 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654742 | GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC | 23603 |
rs748662898 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679985 | TAACCACAGTATCTG[G/T]AATAAAATATCCAAT | 23603 |
rs748719946 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647467 | TCTTGATTGCAGATT[A/G]TGTCTTTTATAGATT | 23603 |
rs748754539 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726620 | TTCAAGACCAGCCTA[A/T]ACAACATAGTGAGAC | 23603 |
rs748755912 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700167 | GCGGGGATCCACTTC[C/T]CCCGCTGTTTTCAGC | 23603 |
rs748784354 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698792 | CACATCCACGTCCCA[C/T]TACAAGTCAGTGACT | 23603 |
rs748795834 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671973 | TCACCATGTTGCCCA[C/G]GCTGGTCTTGAACTC | 23603 |
rs748811750 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715865 | GAGGCCGGGCGGGGT[A/G]GCTCACACCTGTAAT | 23603 |
rs748829332 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666098 | GCTCCCTGAGGAGGT[G/T]ACCTCTAAGGATGAA | 23603 |
rs748889972 | in-del | -/AAGCCTTTAT | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658590 | CAACTGGGGAGACAG[-/AAGCCTTTAT]AAGCCTTCTCTTATT | 23603 |
rs748910105 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647877 | TAACCACCCCAATCA[G/T]TCCATCAAGAGTAAC | 23603 |
rs748918813 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732969 | CTTGTGATAAACGCT[C/G]GACAGTACCTGTTGC | 23603 |
rs748944576 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717065 | TGGCAAGTGCTGGAA[C/T]GCAGAAGAACACAAG | 23603 |
rs748971101 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687748 | CAAGATCGCGCCAGT[A/G]TACTCCAGCCTGGGT | 23603 |
rs749010621 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731644 | GCCACGCCCACTTCC[A/G]GAGGGGAAGCCCGCT | 23603 |
rs749040338 | snp | A/C | 1.66963e-05 | 0.00288927 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678368 | GTGGCCACATACTGT[A/C]GGGTAAGATTTGTCA | 23603 |
rs749065871 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660796 | AGACTGAGGTTCTGA[A/G]AGAACATCAAAAATG | 23603 |
rs749086791 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670766 | GATCCCTTTAGACAA[C/T]ATAAGACTGCTAAAA | 23603 |
rs749151089 | snp | C/T | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648992 | TCATAATAATAGGTT[C/T]ACACTTTCTCTCATG | 23603 |
rs749153256 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724626 | CCTGAGCAATAATCT[C/G]CCAAATCTCCCAAAA | 23603 |
rs749219500 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674813 | GATAAGCAAAGAAAA[C/T]GGTCTCTTGAGATGG | 23603 |
rs749257026 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659660 | TAAAAGGTTTAAATG[A/T]CTGTTTAGGGCACTC | 23603 |
rs749268611 | snp | C/G | 1.64999e-05 | 0.00287222 | intron-variant | CORO1C | GRCh38.p7 | 12:108654290 | TTTAACACCAAACAT[C/G]AAAATTACTGTTTAC | 23603 |
rs749295651 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713518 | AATAACTCAATATCA[C/T]TTAGTTTTTAAAGTT | 23603 |
rs749317480 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653517 | ACTACCTCAACAGCT[C/G]CACTGTTATTAATTC | 23603 |
rs749338921 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683573 | AAGTAGAAATTTACA[G/T]AGTATGAAAACACTA | 23603 |
rs749393233 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723647 | GTCTCTTACACCAAA[C/G]CACCATGTGACCAGA | 23603 |
rs749425361 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695238 | CAACATGGCAGCTCC[A/G]AAAGAGACAAAGTAG | 23603 |
rs749425584 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681622 | TATCATTCAAGAATG[A/C]TGACAAGAAAAAAGC | 23603 |
rs749438076 | snp | C/T | 6.58957e-05 | 0.00573964 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701260 | TCATAGCACTGGTCA[C/T]TTTTCACCGCTTGCC | 23603 |
rs749495640 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702123 | GGATGACAGTAAATG[C/T]GGCAGGAGCACACTG | 23603 |
rs749530545 | in-del | -/TGAT | 1.66352e-05 | 0.00288398 | intron-variant | CORO1C | GRCh38.p7 | 12:108652447 | AGACAAGTCTGTGTC[-/TGAT]TGTTAACTGAAACAT | 23603 |
rs749537172 | in-del | -/AAC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681805 | AGAAAGGTATAGCAA[-/AAC]AACAGTGAGCAAATA | 23603 |
rs749607320 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648610 | TGGTCCTCACCACAC[C/T]GGCCGTGTCTGTGGT | 23603 |
rs749654049 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689215 | TGAAAAAACAAAAAA[A/C]GATGGATCAATCTGA | 23603 |
rs749684362 | snp | A/G | 1.64855e-05 | 0.00287097 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658906 | ATTCCAGATGATAAT[A/G]GCATTATCACAGCCT | 23603 |
rs749689708 | snp | C/G | | | utr-variant-5-prime, intron-variant | CORO1C | GRCh38.p7 | 12:108702992 | AATGATTCGTGGCCA[C/G]GGTCCTTCATTTTGG | 23603 |
rs749694517 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651772 | GAAATGAGGTATTAA[-/T]TCCACAGTACACACA | 23603 |
rs749760161 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691299 | CCACCCCTAATGGGC[A/G]AAGATATTCAACTTG | 23603 |
rs749763663 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680827 | GCTTATCTTATTGCA[G/T]TCTCACAAAAATCAT | 23603 |
rs749773615 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701140 | TTGTGCAGAGGGAGG[A/T]CAAGGAACGCTCCTC | 23603 |
rs749794499 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721574 | ACTTTGTGAATACGA[A/C]TTTTTTAAATGATAC | 23603 |
rs749805456 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677581 | TCTTACGTCACTGTC[C/T]TGTACAGTCTGTGCC | 23603 |
rs749807871 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650325 | CTGGGACCACAGGTA[C/T]GTACTACCACACCTG | 23603 |
rs749827911 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654616 | ACTCACAAAATTTCA[C/T]TGATTTGACAACATA | 23603 |
rs749880420 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719934 | TCACGCCTATAATCC[C/T]AGCACTTTGGGAGGC | 23603 |
rs749892542 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724025 | ATAGAAATCAAGTTT[A/G]CCAAAGGTTTATCCA | 23603 |
rs749913669 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679740 | AACGTGTAAAGACCA[A/C]AGGCTCTGGAATAAG | 23603 |
rs749935441 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666027 | ATGCTGGCATAAGCC[A/G]ACCGCACTACTACGA | 23603 |
rs749980495 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722362 | CTTCAAATTAAGAGA[C/G]AGATGAAGGAGGATG | 23603 |
rs749992864 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676026 | GTAGGGAAAAGAAAA[G/T]GATGAAGGAGGAATC | 23603 |
rs749998915 | snp | C/G | 1.65778e-05 | 0.002879 | intron-variant | CORO1C | GRCh38.p7 | 12:108654413 | CCTGCATATTTTTCT[C/G]GGGGGAAGATAATAA | 23603 |
rs750035308 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712027 | AGACCATTCCAGGGC[A/G]TCGATTACTCAAGCG | 23603 |
rs750061821 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680722 | CAATAAACATTACCC[A/G]AAATTTAACAAATGC | 23603 |
rs750137147 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715494 | ATGTTTACAACCCTC[C/T]ACATCTCCCAATTTT | 23603 |
rs750165621 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725983 | CTGGGACTACAGGCG[C/T]GTGCCACCACACCCG | 23603 |
rs750170789 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732493 | GGGACAGTTCTCTTA[C/T]CTCTTTGGGCCTGAG | 23603 |
rs750178006 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687684 | CAGCTACTCAGGAGG[C/T]TGAGGCACGAGAATC | 23603 |
rs750188850 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701212 | ACAGCACAAAAGGAA[C/G]TATCCCAGGTCACAC | 23603 |
rs750189318 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701417 | GTAGGAAAAACAGAA[C/T]GGTATGGCATTTTGT | 23603 |
rs750209324 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651897 | GGGTGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 23603 |
rs750234716 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699862 | ATCAAATTTGTTCCC[C/T]AAAGGCACCCATCTC | 23603 |
rs750277192 | in-del | -/TCTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665393 | ACTACCTTGGTTAAC[-/TCTT]TCTTGTAACACATTT | 23603 |
rs750305636 | snp | A/T | 1.64762e-05 | 0.00287016 | intron-variant | CORO1C | GRCh38.p7 | 12:108701108 | GTCTACCAGAATGGA[A/T]GATCAAATTACCTAC | 23603 |
rs750357178 | snp | A/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108717755 | CCTTCTGTTGACAAG[A/T]AAGGTATCTGAAAAG | 23603 |
rs750370490 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688635 | ATCTAAGCTGGGCAC[A/G]GTGGCTCACACCTGT | 23603 |
rs750405698 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650387 | GTCTCACTAGATTGT[C/T]CATACTGCTCTTGAA | 23603 |
rs750413715 | snp | A/T | 1.65102e-05 | 0.00287312 | intron-variant | CORO1C | GRCh38.p7 | 12:108654258 | TCTCTGAAGGATAAA[A/T]GTTTCCACTTACAGG | 23603 |
rs750447950 | snp | C/T | 3.30028e-05 | 0.00406205 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657338 | TGCCGCTCGCTCATG[C/T]GGCTGAACCCAGTGG | 23603 |
rs750476181 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676193 | TGGTTACTTTGAGAG[A/G]GAGGAGGGATGTTGT | 23603 |
rs750477242 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708016 | ACAAATCAGAACCCT[C/T]ATACACTCCTGGTGG | 23603 |
rs750622984 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686187 | CGTCTGCACGACACA[G/T]ACTGATTTATCATGT | 23603 |
rs750675264 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709096 | TCTAAAATTGACTGT[A/G]TTGATGGTTGCAGAT | 23603 |
rs750679783 | snp | C/T | 1.66454e-05 | 0.00288486 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658700 | TCACACTCACTCAAG[C/T]GCTCCAACTACTGAG | 23603 |
rs750721703 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684432 | TTCTAGGTGGTCTGG[A/G]TGAGAGAGATGCTCC | 23603 |
rs750731347 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714197 | GGATTGAAACCATCC[A/T]GGCCAACATAGTGAA | 23603 |
rs750734151 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669240 | ATGCTTAGGACTTCA[C/T]GGATTTATACCATAA | 23603 |
rs750813080 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727880 | AGAATACATGAACAA[C/T]TTTTATAACACCAAT | 23603 |
rs750856308 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683141 | TATTAGAAAAGATGC[C/T]AGGTACAGTGGCTCA | 23603 |
rs750857813 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654494 | CCTTATTATATATTC[C/T]TCTATCCCAATTAAG | 23603 |
rs750891789 | snp | C/T | | | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702880 | ACCCTTGGCAGGCAA[C/T]TGAGCATCCACGTTC | 23603 |
rs750921383 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714970 | GAGCGCATTGCAGAG[C/T]GTAATGTGACGCTAT | 23603 |
rs751010613 | snp | A/G | 1.65523e-05 | 0.00287678 | intron-variant | CORO1C | GRCh38.p7 | 12:108662166 | TGCCATACCTGTTGG[A/G]CAAGGAAGAAAGATG | 23603 |
rs751031459 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706875 | AGGTGTGAGCTACCA[C/T]GCCTAGCCGTATTTT | 23603 |
rs751058302 | in-del | -/AG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665581 | TAGAGAGTGAGCACC[-/AG]AGTCAGGCAGAGTCT | 23603 |
rs751086804 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697539 | TAAACCAAAGCAACA[A/C]CTCATGATAAAACTA | 23603 |
rs751161888 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722237 | CATGAATAAAGCCTG[G/T]AGTCATCCCAACCCT | 23603 |
rs751322977 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711761 | ATGCAGACAAGACAG[C/G]GTATTTATATTGCAA | 23603 |
rs751340545 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683341 | GGAGAAGTGCTTGAA[C/T]CTGAGAGGCAGAGGT | 23603 |
rs751404095 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726655 | TCTCTACAAAACATT[-/A]AAAAAAAAAAAAAAG | 23603 |
rs751414933 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723429 | TCATAAGGAAGGGAT[A/G]CTTGTGAATTTTGTC | 23603 |
rs751464900 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679702 | TGACTTGACTGTGCA[A/C]ATCTCCAGGAAAGCA | 23603 |
rs751499689 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722610 | ACGTACCCACCACTT[-/A]ACAATGCTGAATCAA | 23603 |
rs751523459 | snp | A/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647423 | CTGCTATCTTTGCCA[A/T]CTGCTGTTCTAACTT | 23603 |
rs751537384 | snp | A/G | 1.65858e-05 | 0.00287969 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657307 | GGGAGGGCGTACCGG[A/G]TTCCAGAGAGCCAGC | 23603 |
rs751571561 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665901 | ACCTGCCTTCTGTGA[C/G]GCGGTTTGAAGACTA | 23603 |
rs751589060 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658853 | ATCATGTCTGAATGC[A/G]TATCGTCCAAGTTTA | 23603 |
rs751634933 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717606 | CAACTGAATTTAAAA[A/C]TGTTTTAGATATGAA | 23603 |
rs751644971 | snp | A/G | 1.65894e-05 | 0.00288 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658713 | AGTGCTCCAACTACT[A/G]AGTTTTCATCCTAGG | 23603 |
rs751716921 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732221 | CTCCCTTGAGGACTG[C/G]CGACGTTCCAGCCCT | 23603 |
rs751761303 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672939 | CCACCTGCTCTTCCT[A/G]TATTCCTGTCTCTTC | 23603 |
rs751780775 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679948 | TCAGTATTACAATTA[C/T]CTGTAAAATAAGTAA | 23603 |
rs751803958 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725537 | CAGCTAGCAAGAAGC[A/G]GAGCCAAGAGTGAAG | 23603 |
rs751805737 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706698 | CTCCGGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 23603 |
rs751882919 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681228 | CAGAATGAAGTTTGA[C/T]ACACATTTAAATAGA | 23603 |
rs751917415 | snp | C/T | 1.68929e-05 | 0.00290623 | intron-variant | CORO1C | GRCh38.p7 | 12:108652229 | CAAATAATTGTCACA[C/T]AGTTACACCAACCTA | 23603 |
rs751968578 | snp | G/T | 1.65132e-05 | 0.00287339 | intron-variant | CORO1C | GRCh38.p7 | 12:108648937 | TTTGTTTAAAATATG[G/T]ATTGTCTAGAAAACT | 23603 |
rs751996930 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713253 | TCCACTGCTGATATG[G/T]ACTTGTTGAAAAAAA | 23603 |
rs752004173 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693519 | AACAATCAAGGAAAA[C/T]ACCAATTTTGCCAAA | 23603 |
rs752141777 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652484 | GATTATGGGGGTGTC[C/T]CTCTCCTCTACAAAC | 23603 |
rs752294756 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674553 | ACTCCGTCTCAATTT[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs752295574 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714156 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 23603 |
rs752309518 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666565 | GCTACTCTGGGTGAT[G/T]GCCTGCTCGGTTTGG | 23603 |
rs752378080 | snp | A/C/G | 5.01193e-05 | 0.00500575 | intron-variant | CORO1C | GRCh38.p7 | 12:108652257 | CTAGAATACTTGACA[A/C/G]TCTCGATTCTTTACC | 23603 |
rs752380771 | in-del | -/GA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667316 | AGTAAGGACAGATCT[-/GA]GATCTCTGTGCAGGC | 23603 |
rs752395932 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697203 | AACCATGTTTTCAAA[C/T]GGGAGCCTTTCTGAA | 23603 |
rs752414472 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652561 | CATAAAGAGGCTTGC[C/T]TAAAGCATATAAAAG | 23603 |
rs752478252 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677159 | GACATGTGCGAGACT[A/G]CTTACAAATTAATTA | 23603 |
rs752495342 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676670 | CCAGCTACTCGGGAG[C/G]CTGAGGCAGGAGAAT | 23603 |
rs752501806 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665579 | GTTAGAGAGTGAGCA[A/C]CAGAGTCAGGCAGAG | 23603 |
rs752514484 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663588 | CAGACATAGAAGACC[A/G]CATATTGCAGGATTC | 23603 |
rs752547940 | snp | C/T | 1.65181e-05 | 0.00287381 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657328 | GAGAGCCAGCTGCCG[C/T]TCGCTCATGCGGCTG | 23603 |
rs752584961 | in-del | -/TTC | 1.64732e-05 | 0.0028699 | cds-indel, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648687 | TTGCTATCCAGAATG[-/TTC]TTCTTGACCACCTTG | 23603 |
rs752627508 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710292 | CCAAGTTTTCCAGGT[A/G]ATACTGAAGGCCAAA | 23603 |
rs752756933 | snp | C/G | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730427 | TGCCACTTCCCCCAA[C/G]ACATTCAAATCATTT | 23603 |
rs752757568 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648710 | GACCACCTTGAGATC[C/T]CTGTTTTTGCCTGGA | 23603 |
rs752782452 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699411 | GTCTATTTTGTGCTT[C/G]TTAATTGGCTTGTTC | 23603 |
rs752809596 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671036 | AAAAAAAAAGAATAA[A/C]AAAAAAAGGTTTAGG | 23603 |
rs752883305 | snp | A/G | 1.65759e-05 | 0.00287883 | intron-variant | CORO1C | GRCh38.p7 | 12:108662021 | GGACCGCTGAGCTCA[A/G]CTCCCACCTGCACTA | 23603 |
rs752931977 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648528 | GGACAGTACTCGCCG[A/G]CGCCCTGGACCACAA | 23603 |
rs752935481 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701238 | CACACGAGAAACCCG[A/G]ATGTCATCATAGCAC | 23603 |
rs752980288 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687310 | TCTTAAGAAATCCGG[C/T]GAAACCCTGTCCCTA | 23603 |
rs753013711 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692401 | GTCTAAAACAGAGTA[C/T]CACAATGTGTAGAAA | 23603 |
rs753045290 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717366 | AGGATTTTATCTGTA[C/T]TTGCAGTCTTGGGAG | 23603 |
rs753072381 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713717 | GCAGTGACCTTGAAC[C/T]ACAAAGTACGGAGCA | 23603 |
rs753129444 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724055 | AAGAGATATCATGTA[A/T]TTTCAAGTTTCCTAA | 23603 |
rs753148064 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705182 | GAAGGGAATGATACC[C/T]GTAATAAGAATGTAG | 23603 |
rs753162017 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689640 | GAAGATGTAAGGGCC[G/T]AAGAGCCCCCACCCC | 23603 |
rs753187933 | snp | A/G | | | intron-variant, missense | CORO1C | GRCh38.p7 | 12:108657532 | ATTCATGTTCACCTG[A/G]GTGTGGGAGGGAGGT | 23603 |
rs753225218 | snp | A/G | 1.6651e-05 | 0.00288535 | intron-variant | CORO1C | GRCh38.p7 | 12:108652452 | AGTCTGTGTCTGATT[A/G]TTAACTGAAACATCT | 23603 |
rs753264131 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667943 | GTGCTAATTTTAAAG[C/T]ACAATTAGTTAAATA | 23603 |
rs753278155 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658659 | CCACTGACCAGTACC[A/G]CTGCCTGCCTTAAAA | 23603 |
rs753288003 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658875 | CCAAGTTTATAAGGG[C/T]TTCCCCTGTTCCCAC | 23603 |
rs753356066 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652221 | TCCAAGTACAAATAA[C/T]TGTCACACAGTTACA | 23603 |
rs753362647 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650772 | ACAACTGTGTTTATA[A/G]TCTGTCGAACTTTTA | 23603 |
rs753392946 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718792 | AAAACACTCAATATC[-/A]GTATCTATAATAGAG | 23603 |
rs753448583 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652307 | AACATCAAGTCCCCT[C/T]TTGGGCATGTAACCC | 23603 |
rs753453125 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701187 | GATTATGGCAACAAA[C/T]CTGGGATTGACAGCA | 23603 |
rs753543104 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701509 | GACAACTGCAAAATG[C/T]GTCAGGGAAAGAATT | 23603 |
rs753609103 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719390 | TTTGTGACCACTTAT[C/T]GTGAATACAATATAA | 23603 |
rs753736406 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702539 | CCTATGTGCTACTGC[A/G]GGACATTCTGTTCAT | 23603 |
rs753759327 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704025 | GAGGAAGGCCTCTCA[C/T]TTGAAAAAGAGAGAC | 23603 |
rs753769943 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720818 | ATGAGCCACCGCACC[C/T]GGCAAATATTTACAA | 23603 |
rs753818052 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696732 | AGAATAAGTAAATGC[A/C]CTAAGCCACACCTTG | 23603 |
rs753829758 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676609 | AAACTCCGTTTCTAC[C/T]AAAAACATAAAAATT | 23603 |
rs753831660 | snp | A/C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676543 | TTGGGAGGCTGAGGC[A/C/G]GGGGGATCACTTGAG | 23603 |
rs753864262 | snp | A/C | 0.000193143 | 0.00982519 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702821 | CATGTGTGAAAGTGG[A/C]CTCTCTCCAATGCTG | 23603 |
rs753912061 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709231 | TATAAAGTACTCAGC[A/G]TAGAATCTGAAGCAT | 23603 |
rs753934697 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678092 | AAGGGCTTCTTGAAA[C/G]GATTATCTGTAATTA | 23603 |
rs754013840 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689154 | GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC | 23603 |
rs754024191 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648809 | CAGCGCGGCCTCTGG[C/T]CCCGCTGTGTCAGGA | 23603 |
rs754059927 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654452 | ATATGTGTATGTATA[C/T]ATTTTTTTAAAAATA | 23603 |
rs754080195 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728888 | AACACAGAGAAGTCA[C/T]AAATGGAAAACAAGC | 23603 |
rs754098428 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698010 | ATTCTATTTTCTACC[A/G]GCTACTGATGCCTGG | 23603 |
rs754127578 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657174 | TAAGAACTTCACATC[C/T]AATCTAAGACAATCA | 23603 |
rs754151240 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716024 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 23603 |
rs754176044 | snp | C/T | 4.96233e-05 | 0.00498088 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662049 | CTAAGAAGCACATTG[C/T]GGGCCGTTGGATGCC | 23603 |
rs754195340 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730283 | GATGTGTTTCTAAAT[C/T]GTGATGCAGTAAAGC | 23603 |
rs754239353 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715051 | AACAGTAACACATAA[C/T]GAACCTGAAGACAAA | 23603 |
rs754292568 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658298 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 23603 |
rs754336284 | snp | A/C | 3.29962e-05 | 0.00406165 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662125 | CAGGTTCAGTCAGGG[A/C]AAGGGTGAGTCCATT | 23603 |
rs754347310 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704752 | TTCTTGCACAGAATG[C/T]CTCAGGCCCTCCAGG | 23603 |
rs754397581 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715948 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 23603 |
rs754406967 | in-del | -/CAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660451 | AGCGAAACTCCATCT[-/CAA]AAAAAAAAAAAAAAA | 23603 |
rs754430834 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648732 | TTGCCTGGAATGTAC[A/C]CGTGCTTCAAGGAGA | 23603 |
rs754504712 | snp | A/T | 1.65908e-05 | 0.00288012 | intron-variant | CORO1C | GRCh38.p7 | 12:108662180 | GACAAGGAAGAAAGA[A/T]GATCCACATGAAAGC | 23603 |
rs754520958 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719136 | CTTGAAAATTATAAT[A/C]TTTAATTCTCTATGC | 23603 |
rs754541247 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713101 | AAAAAAACATGCCTT[A/G]CCTATTTTAATAGAA | 23603 |
rs754547081 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700260 | ACTGGAGCTCAGGAC[C/T]CACCAAACTCATTTT | 23603 |
rs754552877 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667022 | TCATGGCTTACTGTG[A/C]GGATACAATAACTAA | 23603 |
rs754626262 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693888 | CTTCTCTGTGATGTC[C/T]TCCTTACCTTCTAAG | 23603 |
rs754641866 | in-del | -/CA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691527 | TGTCAGCCTGCTTAG[-/CA]CAGACTGGCACGCTC | 23603 |
rs754654230 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692776 | AATGCAAAGGATTCA[A/G]TGTCCATTAGACCAC | 23603 |
rs754666935 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733190 | GTTTTTGTTTGTTTG[A/G]GACACAGTCTTGCTC | 23603 |
rs754681530 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669359 | GTCTATTAAAGGTAC[G/T]CTTGCTGCTAGGAAT | 23603 |
rs754730450 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707754 | TAAGACACTTGTATC[-/T]AGAGTATAAAAAGAA | 23603 |
rs754737575 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701516 | GCAAAATGCGTCAGG[A/G]AAAGAATTACAAAGA | 23603 |
rs754779075 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662500 | AAATGTAATATGTTA[A/T]CGGAGATCAGGATAC | 23603 |
rs754806443 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676937 | TAGCTGCCAAAATTA[A/T]GAGATCACAGGAGGA | 23603 |
rs754815325 | snp | C/T | 1.68596e-05 | 0.00290336 | intron-variant | CORO1C | GRCh38.p7 | 12:108654444 | TAATACATATATGTG[C/T]ATGTATACATTTTTT | 23603 |
rs754817920 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657477 | AAGAAGACAAGGTGA[A/G]TGGAGAAACTCGGGC | 23603 |
rs754823875 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673144 | AGGCCAAAAGCTAAG[C/T]GCCTCTTAAGCCAGT | 23603 |
rs754917870 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674946 | GAGAGGACTGACTCC[A/G]ATTTTGAAAGAAGTT | 23603 |
rs754972843 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | CORO1C | GRCh38.p7 | 12:108648585 | CCAGCCAAGCACCCC[C/T]GCACTCCACTGGTCC | 23603 |
rs755025882 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658855 | CATGTCTGAATGCAT[A/G]TCGTCCAAGTTTATA | 23603 |
rs755094723 | snp | A/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647452 | TTGGAAATACGCTCA[A/T]CTTGATTGCAGATTG | 23603 |
rs755113844 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715066 | TGAACCTGAAGACAA[A/G]AGATAAAATTCCTAA | 23603 |
rs755126822 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669477 | ATTATTATCATACCT[C/T]CATATTATATGGAAG | 23603 |
rs755152346 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646062 | TGCGGAGGGACATGT[C/T]TGTATGCATTAAAGC | 23603 |
rs755205970 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729023 | TTAATAATATGTTTC[C/T]AAAGTACCAGTTTGT | 23603 |
rs755232996 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686142 | GAAAGACATTTTGCA[C/T]TAGGATCTAATAAGA | 23603 |
rs755242174 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647241 | TGGGAGACAAATTGA[C/G]TTCTTACTGGAATGT | 23603 |
rs755281758 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728713 | AAAGGATCTGAACTA[-/G]GGCAAAGAAAACCCA | 23603 |
rs755300140 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711136 | GGGAGGACAAGGCAG[A/G]AGGATGACTAGAGTC | 23603 |
rs755322771 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684684 | GTATTCTACCTGTAT[C/G]TGTTATGCTTTATTA | 23603 |
rs755348621 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704167 | CTTCTGGCTGACATA[C/T]ATACTAAACTACCTT | 23603 |
rs755464033 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655997 | CTGCTCCGCCGCCCC[A/G]TCTGGGATGTGAGGA | 23603 |
rs755490603 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722447 | GGACGCCACACAGCC[G/T]GCACAGGGAGGCTCC | 23603 |
rs755495316 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713370 | AACACCAGGAATGGT[-/A]AAAATTAAGGGAAAA | 23603 |
rs755502319 | snp | A/T | 1.65608e-05 | 0.00287752 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658721 | AACTACTGAGTTTTC[A/T]TCCTAGGAATACTCA | 23603 |
rs755519769 | in-del | -/TT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677559 | TTTTATCTGCATAAC[-/TT]TGGCATCTTACGTCA | 23603 |
rs755538627 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684065 | AACAGACAAGTTACA[A/G]AGTGCAAGAAGAGGT | 23603 |
rs755542133 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691395 | AATGTGTTCATGACA[C/T]CTTGAGTTTATTTCA | 23603 |
rs755544339 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704777 | TCCAGGCACACAATA[C/G]AGTATAGCAATTAAG | 23603 |
rs755580434 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710889 | TACATGTTGGGTGAA[G/T]ATTTTAACCAAGAAC | 23603 |
rs755602768 | snp | C/G/T | 3.30029e-05 | 0.00406209 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648986 | GAACAGTCATAATAA[C/G/T]AGGTTCACACTTTCT | 23603 |
rs755637993 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714010 | AGACAAACAAGAGGG[C/T]ATCTGTTATGACCAA | 23603 |
rs755757086 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699936 | CCACTGAAGTAAAAA[C/T]CAGATGTTATAATAA | 23603 |
rs755796480 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688672 | AGCACTTTGAGAGGC[C/T]GAGGCAGGTGGATCA | 23603 |
rs755801715 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690384 | GGGAGTATGGGCCTA[A/C]AGAGACTTCACCTGC | 23603 |
rs755868160 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728311 | AAACAAAATACGGCA[C/T]ATCCAAACAATGGAA | 23603 |
rs755880498 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701490 | TTAGCAGCACATACC[C/G]GGAGACAACTGCAAA | 23603 |
rs755887660 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712146 | CCACTGTTACCTGTA[C/T]GGCAGGTACTTTAAT | 23603 |
rs755890956 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726035 | AGAGACAGGTTGGCC[A/G]TGTTGGCCAGGCTGG | 23603 |
rs755920623 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674663 | CATTTGAGGAGTTCA[A/G]GACTTTGGTGGAAGA | 23603 |
rs755938010 | snp | A/G | 6.62701e-05 | 0.00575593 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678353 | CAGCACTGGTCCTGT[A/G]TGGCCACATACTGTA | 23603 |
rs755956120 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687693 | AGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 23603 |
rs755991842 | in-del | -/CTGA | 3.31444e-05 | 0.00407076 | intron-variant | CORO1C | GRCh38.p7 | 12:108649068 | AAGTGAAATATGAGG[-/CTGA]CTAACAGGATGAATA | 23603 |
rs755993301 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700318 | TGTTTCTAGGCCCTC[C/T]TCACAGCTTTTTTTT | 23603 |
rs755994305 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715755 | GAGCAGAACACAACT[-/C]CAAAGAGCCAAATTA | 23603 |
rs756035728 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719350 | ACACGTATACACACA[A/C]ATGCAATTACAAAAT | 23603 |
rs756073354 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650425 | GCTCAAGTGATCCTC[C/T]CACCTTGGCCTCCCA | 23603 |
rs756073401 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706803 | TGGTCAGACTGGTCT[C/T]GAACTCTTGACCGCA | 23603 |
rs756113158 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673317 | CAAAGCCTAATCCAG[A/G]GCAAAGTCCTAACTC | 23603 |
rs756126202 | snp | C/G | 8.5357e-05 | 0.00653232 | intron-variant | CORO1C | GRCh38.p7 | 12:108678221 | ACATGCTTTTGAAAG[C/G]AGTAGGTGAGTCTCA | 23603 |
rs756272861 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708057 | TGTTGCAGCTGATGT[C/G]GAAAAGTCTGAAAGT | 23603 |
rs756277229 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648713 | CACCTTGAGATCCCT[A/G]TTTTTGCCTGGAATG | 23603 |
rs756284147 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | CORO1C | GRCh38.p7 | 12:108654275 | TTTCCACTTACAGGA[C/T]TTAACACCAAACATC | 23603 |
rs756284671 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727918 | CAACCCATTAAAAAA[C/T]GGGCAGAGCATTTGA | 23603 |
rs756341452 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701248 | ACCCGGATGTCATCA[C/T]AGCACTGGTCATTTT | 23603 |
rs756377363 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696468 | CACTGGTGTGTATGA[A/G]CCCTCCATGGTTCAC | 23603 |
rs756380690 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662404 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 23603 |
rs756386649 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646263 | TGTGAGGAAGAGGGT[-/AG]AGAGCAGGAGCTTTG | 23603 |
rs756418592 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656902 | AAGTACCCAGGGACA[C/T]AAACACTGCGGAAGG | 23603 |
rs756472501 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714206 | CCATCCTGGCCAACA[C/T]AGTGAAACCCCATCT | 23603 |
rs756479038 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654511 | CTATCCCAATTAAGC[A/G]AGCCATTTTCCTAGA | 23603 |
rs756516563 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659020 | CATATGTATATGCAG[-/AG]AGAGAGAGAGAGAGA | 23603 |
rs756569073 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658756 | AACAATCTCTTGTTT[C/G]CTGGGATCAATGACT | 23603 |
rs756625631 | in-del | -/CAAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683751 | CCCATCACCACCTCC[-/CAAT]CAATCAATCAATCAG | 23603 |
rs756648744 | in-del | -/TT | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730252 | CAAGGGCAGCCTACA[-/TT]ACGGCCAAATATAGG | 23603 |
rs756667040 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715017 | AATCAAGTCTGACAA[C/G]AAGTAAAATGAGCAG | 23603 |
rs756699217 | snp | G/T | 0.000168421 | 0.00917508 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702913 | TAGCCCAGCTGTTAT[G/T]GCCAGACTTTCCCAG | 23603 |
rs756720871 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721457 | TACTGCAGAATTCAC[C/T]ATCAAAGAGTCATGT | 23603 |
rs756734816 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658883 | ATAAGGGCTTCCCCT[G/T]TTCCCACATTCCAGA | 23603 |
rs756739626 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691188 | TCAATTCAGTCAGCC[A/G]GAAATGAAACCCAAG | 23603 |
rs756759301 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678627 | GTAACCAACTGCACT[A/G]GCAGACATAGCAAAA | 23603 |
rs756808159 | snp | A/C | 1.66932e-05 | 0.002889 | intron-variant | CORO1C | GRCh38.p7 | 12:108652457 | GTGTCTGATTGTTAA[A/C]TGAAACATCTGGATT | 23603 |
rs756813141 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657107 | ACAGCCTCTTCAGGA[A/G]TATCAAAAGTATGTC | 23603 |
rs756843082 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663832 | GAATTCTATGTGAAT[G/T]ATATCTCAATAAAAC | 23603 |
rs756869306 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658915 | GATAATGGCATTATC[A/G]CAGCCTAAAACAGGC | 23603 |
rs756896027 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710777 | CCATGTTGGCCAAGA[C/T]GGTCTCGATCTCTTC | 23603 |
rs756900402 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672086 | TATATTCAGAGAAAC[C/T]CACTTTCAAGTAAAA | 23603 |
rs756913182 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709611 | CATATCACCAAACTT[A/C]GGAGTTCTGTTATCA | 23603 |
rs756953744 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679710 | CTGTGCAAATCTCCA[A/G]GAAAGCAGAACGTTA | 23603 |
rs756987687 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722322 | CATGATTTAAAGAAA[A/G]TGAGCTTAACCAGGG | 23603 |
rs757013278 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711806 | ATACACTCAAAACAC[A/C]TGAGTAAATGTTACA | 23603 |
rs757142016 | snp | A/C/G | 4.94322e-05 | 0.00497132 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652310 | ATCAAGTCCCCTCTT[A/C/G]GGCATGTAACCCATC | 23603 |
rs757147210 | snp | A/G | 1.67461e-05 | 0.00289357 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678371 | GCCACATACTGTAGG[A/G]TAAGATTTGTCAATT | 23603 |
rs757163279 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687441 | GCAGTGAACTATGAT[C/T]GCGCCACTGCACTCC | 23603 |
rs757195237 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648669 | TTCTTGTTTGCAGTG[C/G]GCTTGCTATCCAGAA | 23603 |
rs757214815 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716796 | TCACTGCAAACCACA[C/T]TACTTACTAACATCC | 23603 |
rs757224673 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665928 | ACTAACATGGTAACA[C/T]GAAACTGACACATTT | 23603 |
rs757250902 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699554 | TAACAAGCTATGGCT[C/G]TCTTCTCAGTTGGCT | 23603 |
rs757252980 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686518 | TTGCTTAATCTAGAA[C/T]ATTACTACTTTTCTG | 23603 |
rs757268111 | in-del | -/ATTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725801 | AAAGGTGCTAAGTGA[-/ATTT]ATTTATTTATTTATT | 23603 |
rs757306545 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | CORO1C | GRCh38.p7 | 12:108701101 | AGAGGGTGTCTACCA[A/G]AATGGAAGATCAAAT | 23603 |
rs757315149 | snp | A/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704467 | ACATAGCAAGATTCC[A/T]TCTCAAAAAAAAAAA | 23603 |
rs757361855 | in-del | -/AT | 9.98951e-05 | 0.00706665 | intron-variant | CORO1C | GRCh38.p7 | 12:108654435 | AGATAATAATAATAC[-/AT]ATATGTGTATGTATA | 23603 |
rs757414655 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692457 | GTAAGGCAGACATGC[-/A]AGCCAATGCAAATCC | 23603 |
rs757420842 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717611 | GAATTTAAAACTGTT[C/T]TAGATATGAAGGGTG | 23603 |
rs757467310 | snp | A/G | 4.95282e-05 | 0.00497611 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657331 | AGCCAGCTGCCGCTC[A/G]CTCATGCGGCTGAAC | 23603 |
rs757484967 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725172 | GGTGTTTTTAAGACC[A/G]CCTTCCCATCCTAAA | 23603 |
rs757585311 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681275 | AATTAAAAGAATGGA[A/T]CAGAGGCAAAAATTA | 23603 |
rs757612540 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725547 | GAAGCGGAGCCAAGA[C/G]TGAAGCCCAGCTCTA | 23603 |
rs757613425 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706720 | CTGTCTCAGCCTCCC[A/G]AGTAGCCGGGACTAC | 23603 |
rs757747152 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701573 | AGAAACAGCTCATCA[C/G]TTTTAATTTCAATGG | 23603 |
rs757827274 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667049 | CTAAATATTATCATG[C/T]ACATAAAGGCTTAGA | 23603 |
rs757828061 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648812 | CGCGGCCTCTGGCCC[C/T]GCTGTGTCAGGATAC | 23603 |
rs757832926 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713257 | CTGCTGATATGGACT[G/T]GTTGAAAAAAATGTT | 23603 |
rs757835394 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652188 | TCAGATATTTTTGAG[A/T]TCTGAAGTATATGCT | 23603 |
rs757863204 | snp | A/G | | | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702805 | TCTTACCCTTCCAAC[A/G]CATGTGTGAAAGTGG | 23603 |
rs757883118 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648733 | TGCCTGGAATGTACC[C/T]GTGCTTCAAGGAGAT | 23603 |
rs758002895 | in-del | -/AAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660453 | CGAAACTCCATCTCA[-/AAA]AAAAAAAAAAAAAAA | 23603 |
rs758009058 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652579 | AAGCATATAAAAGTT[C/T]CTTTTCCTCACAAAG | 23603 |
rs758021073 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721266 | CTATTATCATCACTT[C/T]CCATAATCAGGGCCA | 23603 |
rs758037945 | snp | C/T | 3.31263e-05 | 0.00406965 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662149 | GTCCATTTTCTGGGA[C/T]CTGCCATACCTGTTG | 23603 |
rs758061975 | snp | C/G | 4.94246e-05 | 0.0049709 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648749 | GTGCTTCAAGGAGAT[C/G]AGGATTGGGTCTGCA | 23603 |
rs758095318 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654218 | GAAAAATTAAACAGA[C/T]ACAACACATTGCCCG | 23603 |
rs758191691 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690258 | GAGGCTTTACTTTAA[A/G]GGAACCAGAAATACC | 23603 |
rs758193447 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709380 | TTCATATAAAAGAAC[C/T]GGCACCACTTATCAA | 23603 |
rs758237818 | snp | A/G | 6.58935e-05 | 0.00573955 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701220 | AAAGGAACTATCCCA[A/G]GTCACACGAGAAACC | 23603 |
rs758285909 | snp | C/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652344 | CTCTGAGGCTCCTTG[C/G]TGCTGAATGTGTTGA | 23603 |
rs758301381 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698284 | GGGGACAAAAATGGA[A/T]CAAAACTGTTTTCTT | 23603 |
rs758325466 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662870 | CTTCAAAGGACACTA[C/T]GAAGAAAGTGAAAAA | 23603 |
rs758363198 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729277 | ATTCACTGACACCGA[A/G]TCTAATCCTAAACTA | 23603 |
rs758392021 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710507 | AAAATGTAAAAGCTG[A/G]TAACTAATATTCATA | 23603 |
rs758414037 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657605 | TACTATGTGATCTGG[-/A]TCAAGGTCCCTCTGT | 23603 |
rs758419782 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672900 | ACTTCATCGATAAAC[A/G]CTGTGTGTTTTCTCA | 23603 |
rs758447725 | snp | C/T | 4.95233e-05 | 0.00497586 | intron-variant | CORO1C | GRCh38.p7 | 12:108654262 | TGAAGGATAAATGTT[C/T]CCACTTACAGGATTT | 23603 |
rs758450996 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728777 | GGTCATACTGAAATA[C/T]TCATGAAGAATTCTG | 23603 |
rs758475594 | snp | A/G | 3.30502e-05 | 0.00406497 | intron-variant | CORO1C | GRCh38.p7 | 12:108701339 | CTGCAAAGGAAGAGT[A/G]AGAATTATGTTAGAA | 23603 |
rs758547610 | snp | A/G | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730473 | GGGGAGCGTGCGCCG[A/G]TGGGGACAGGCGGGA | 23603 |
rs758591026 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680316 | TATGGCCCTGTTTAC[-/A]AGACCTAAGGCCTAG | 23603 |
rs758701110 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648814 | CGGCCTCTGGCCCCG[A/C]TGTGTCAGGATACAG | 23603 |
rs758736712 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694391 | TTCTAAAGTACTGTG[-/T]TTAAATTTCACAAAC | 23603 |
rs758770980 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715443 | TCAATGACAGAAATA[C/T]ATATTTCTATTACAG | 23603 |
rs758779455 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692503 | AGACTGTGGATCACA[C/T]AGAAAAGCACTGTCA | 23603 |
rs758883297 | snp | A/C | 0.000332226 | 0.0128842 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702853 | GGGCATGTAGCCGGG[A/C]TGAAGTAAGAGACCC | 23603 |
rs758883456 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681159 | GTGTGTGCCACCATG[A/C]GTGGCTTGAATGTGT | 23603 |
rs758925057 | snp | A/C | 0.000151836 | 0.00871177 | intron-variant | CORO1C | GRCh38.p7 | 12:108647532 | ATTTTGCTAAGAAAA[A/C]AAAAAAAGGAGGCAG | 23603 |
rs758932141 | snp | G/T | 1.66346e-05 | 0.00288393 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658703 | CACTCACTCAAGTGC[G/T]CCAACTACTGAGTTT | 23603 |
rs758932186 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712180 | GAAGAGATCCGATGT[A/G]TTATTCAATAGAAAA | 23603 |
rs758935295 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689704 | GACCTGACTCAAAGA[A/G]CAGTTAAAAGATTTC | 23603 |
rs758973624 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680051 | AATTTACTCCATCAT[A/T]AAGAATTAACAAATA | 23603 |
rs758975367 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693433 | GATACAAACGAAAGA[C/T]GCCATGTTGATCTAG | 23603 |
rs759051290 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669007 | TGTAGTTTCTGGGAG[C/T]ACAATTTACACAACT | 23603 |
rs759059885 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648425 | CTCCGTTAAAGGAGG[-/C]CAAGTGTTGCCACAA | 23603 |
rs759064474 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651752 | CACTTCAGTTATATG[A/G]GCAGGAAATGAGGTA | 23603 |
rs759088338 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715614 | AAGACAAAGGCAGGC[A/G]CTACCTGACCCGCCT | 23603 |
rs759119018 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696031 | ATGGGAGAAACACAG[C/T]TGTGTATAAGAAAGT | 23603 |
rs759210917 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108645807 | GCAAGAATTCCCTTC[A/G]TGGTCCCAATGGCAC | 23603 |
rs759233826 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714761 | CAGTGATACCCAAAA[A/T]AAATAAAAATAAAAA | 23603 |
rs759341982 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704364 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGGAA | 23603 |
rs759370733 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663904 | GAAGACTCACCACAT[C/T]TTAATTGGGGACATG | 23603 |
rs759427616 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703700 | AGGAGCAGCTGGACA[A/C]CCAGATCCCAGGGCT | 23603 |
rs759505954 | snp | A/G | 1.66941e-05 | 0.00288908 | intron-variant | CORO1C | GRCh38.p7 | 12:108657468 | TTAAACTGCAAGAAG[A/G]CAAGGTGAGTGGAGA | 23603 |
rs759506129 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678117 | TAATTAAACTTAAAC[A/G]TAGTAAATTATTGTA | 23603 |
rs759511658 | in-del | -/TATAGTAGAC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683029 | AAAAATGGACAGTCT[-/TATAGTAGAC]TAAATGCATATAGTA | 23603 |
rs759533661 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708597 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCGCCTGC | 23603 |
rs759533856 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691808 | AGCTGGCCAAGGAAA[C/T]GCACAAAGGCTGCCT | 23603 |
rs759545300 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645589 | ATTAAACACATACAT[-/AC]ACACACACAAAACCA | 23603 |
rs759551227 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710288 | CTCACCAAGTTTTCC[A/G]GGTGATACTGAAGGC | 23603 |
rs759576042 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679411 | TTTGAATCTAGCAAA[C/G]CAACCAGGGTTATCA | 23603 |
rs759607019 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648425 | ACTCCGTTAAAGGAG[A/G]CAAGTGTTGCCACAA | 23603 |
rs759620406 | snp | A/C | 6.64584e-05 | 0.0057641 | intron-variant | CORO1C | GRCh38.p7 | 12:108662010 | AGACAAGGGGAGGAC[A/C]GCTGAGCTCAGCTCC | 23603 |
rs759627552 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723231 | AGCGCACTTTCACGT[A/G]TGTTCCTCAGTCCCC | 23603 |
rs759679794 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716823 | ATCCACAGGGTTATA[C/T]GTATTACATATATAC | 23603 |
rs759803302 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665328 | TCCAGCTGGTTTAAC[A/G]GTTCCCTCAGCTGGG | 23603 |
rs759831598 | snp | A/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731964 | CCGAGTCCTTAAACC[A/T]GCCTCCTGCTTCCCT | 23603 |
rs759854530 | snp | C/G | 1.65795e-05 | 0.00287914 | intron-variant | CORO1C | GRCh38.p7 | 12:108652431 | CCCTGTAAGAAACCA[C/G]AGACAAGTCTGTGTC | 23603 |
rs759869408 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711385 | AAAACACAAAATACA[A/G]AAGAAAGAAAAGGGC | 23603 |
rs759897481 | snp | G/T | 1.67539e-05 | 0.00289425 | intron-variant | CORO1C | GRCh38.p7 | 12:108652251 | ACCAACCTAGAATAC[G/T]TGACAATCTCGATTC | 23603 |
rs759898886 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674859 | ACGACGCTGTGAACA[C/G]TGTTGAAATGACAAC | 23603 |
rs759957370 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701150 | GGAGGACAAGGAACG[C/T]TCCTCCCCCACTTGC | 23603 |
rs759977031 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649716 | TTCTCTTATGATGAC[C/T]CTGATAAGGTCAAGC | 23603 |
rs759982152 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674298 | CTGGGCACGGTGGCT[C/G]ACACCTTTGGGAGGC | 23603 |
rs760019690 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717327 | GCAGAACCCGGATCA[C/G]AGAGGGCTTTCTAGG | 23603 |
rs760169749 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680803 | ACTAGGTCTAAGCCA[C/T]GTGGTTTTGCTTATC | 23603 |
rs760176286 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672462 | TTTTCACTCTGAGAC[G/T]ATTACATGTATAACG | 23603 |
rs760203886 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693402 | GTGACAGAAGTCACT[A/G]CTTTTTCCTAAAGAT | 23603 |
rs760213889 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687155 | CCAATGGGCATTTTG[C/T]GGGGAGAAAGTGAAT | 23603 |
rs760234276 | snp | C/T | 1.66192e-05 | 0.00288259 | intron-variant | CORO1C | GRCh38.p7 | 12:108652443 | CCAGAGACAAGTCTG[C/T]GTCTGATTGTTAACT | 23603 |
rs760283072 | snp | C/G/T | 3.29464e-05 | 0.00405861 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701171 | CCCCACTTGCCTCTA[C/G/T]GATTATGGCAACAAA | 23603 |
rs760292777 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676096 | AAACTGGCAAGACCA[A/G]TCTAGAGTCTAGAGG | 23603 |
rs760296924 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733165 | GGTGAGGCTCAAAAA[C/G]AATTCACTTGTTTTT | 23603 |
rs760325300 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660057 | AAGCAAAATACGGGA[A/G]GGACATCCTAGAGGT | 23603 |
rs760346215 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678568 | CCACTACCAAGGACA[C/T]GCGATCAAATTACAA | 23603 |
rs760356719 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659538 | TTTCTGTGCACATAC[A/G]TAAATTATTTTACAT | 23603 |
rs760372830 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727033 | TTCATGATAATCAGA[A/G]AAACCCACTGACCTC | 23603 |
rs760426637 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658825 | GCCATTCCGGTTCCA[A/G]CTCACATTGTAAATC | 23603 |
rs760449867 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702514 | CCTAGACTGCACCCA[A/G]TGTAATTTTCCTATG | 23603 |
rs760460558 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724966 | ACACTTTATCACACT[A/G]TAACCAGAAGAGTTA | 23603 |
rs760487454 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667855 | GTGAAAGCCTGGATA[C/T]GGAAAAAGGACAACT | 23603 |
rs760509955 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703406 | TAAAATGAAAGCAAA[A/C]AATAAAAGCAGGTAA | 23603 |
rs760519774 | snp | A/G | 6.60273e-05 | 0.00574537 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662078 | CCAAGCCACGATGCC[A/G]ACTCTCTTTGAGTGG | 23603 |
rs760562050 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684033 | GCAGTGTGAGTTGTT[C/G]TTTAAAAATGTAAAT | 23603 |
rs760568743 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713848 | AGAGCTCTGTCCTGT[A/G]GGTGCTGCTTTGACA | 23603 |
rs760615495 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662264 | TATGTAAACAGAACA[C/T]AGAGTGATATCTGGA | 23603 |
rs760645802 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689443 | CACACACAATTTCTT[C/T]CAAGTTTGCATTCTG | 23603 |
rs760649978 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730147 | CTTTGTATCTTACCA[C/T]GCCGGGGGAAATGAA | 23603 |
rs760713882 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668845 | TTGACTGCTCTTTGT[A/T]TTATTTAAAGCACTA | 23603 |
rs760740496 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651907 | GTGGGCGCCTGTAAT[A/C]CCAGCTACTTGGAAG | 23603 |
rs760764215 | in-del | -/AAAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660452 | GCGAAACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 23603 |
rs760780302 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676373 | TTTTATAATACACAC[C/T]ATTTTTTTTAAAAGG | 23603 |
rs760797929 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648803 | TGCCTCCAGCGCGGC[C/T]TCTGGCCCCGCTGTG | 23603 |
rs760852964 | snp | A/G | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662117 | AATCACCACAGGTTC[A/G]GTCAGGGAAAGGGTG | 23603 |
rs760927153 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710139 | AACTATTCTAGAATG[C/G]TTTTTATTATAATAA | 23603 |
rs760954838 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670632 | AGCAGCTATCTGAAC[C/T]AAGCCACCATTTAAA | 23603 |
rs761018453 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699143 | AGCAACTTATTCTAT[C/G]CTAGTTCCCATAATG | 23603 |
rs761058133 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685724 | CTCTGGTTGTGATGT[C/T]ATCATAAATCCTTAA | 23603 |
rs761109962 | snp | A/C/T | 4.94836e-05 | 0.00497391 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654343 | CTGGTGTCAGGGTCA[A/C/T]AGAAAGGCAGCAACA | 23603 |
rs761113717 | in-del | -/TAGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668564 | GAAGCAAAAATGGAT[-/TAGA]TAGGGTATTTTTGTT | 23603 |
rs761122690 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648179 | GCTACATCTGAACAC[C/G]TGCCACTCCCTCCTT | 23603 |
rs761222799 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659919 | GAAAGAAGCCCACAA[C/T]GTCAACTCATTCACC | 23603 |
rs761246249 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706151 | GAGACAGTGCCACTG[A/C]ACTCCAGTCTGGGCA | 23603 |
rs761254126 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687001 | CCAGCAACCTTCACC[A/G]TGGCAGAAACCGTCC | 23603 |
rs761260281 | snp | A/G | 1.65315e-05 | 0.00287498 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662045 | TGCACTAAGAAGCAC[A/G]TTGCGGGCCGTTGGA | 23603 |
rs761261695 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729750 | GAACCAAGTCCAAAA[C/T]AGATTTTGCACATTT | 23603 |
rs761330254 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688371 | CAGACACGTCTCAAT[-/A]AAGTTCTGTGCTGGG | 23603 |
rs761404466 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704651 | TCAGGCATCTCTAAG[C/T]GGAGCTTGAAGGGCA | 23603 |
rs761426216 | snp | A/G | 1.65187e-05 | 0.00287386 | intron-variant | CORO1C | GRCh38.p7 | 12:108701335 | GTGTCTGCAAAGGAA[A/G]AGTGAGAATTATGTT | 23603 |
rs761442672 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699832 | GCCAATAAGAAGGTA[C/T]ATTTGAAAACACGTA | 23603 |
rs761501503 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703527 | GTAACTGACTGAAGT[G/T]TGAGTGTCCTCTACT | 23603 |
rs761515371 | snp | C/G | 1.66579e-05 | 0.00288595 | intron-variant | CORO1C | GRCh38.p7 | 12:108661992 | GAGAGCCACAAGAGT[C/G]GAAGACAAGGGGAGG | 23603 |
rs761532317 | snp | G/T | 1.67354e-05 | 0.00289265 | intron-variant | CORO1C | GRCh38.p7 | 12:108657291 | GCAAGTGGAAAGCCT[G/T]GGGAGGGCGTACCGG | 23603 |
rs761544630 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648661 | GGTCGCACTTCTTGT[C/T]TGCAGTGGGCTTGCT | 23603 |
rs761573773 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658202 | CATTTATTTATTTAT[C/T]TATTTATTTATTTTT | 23603 |
rs761596232 | snp | C/T | 1.64939e-05 | 0.0028717 | intron-variant | CORO1C | GRCh38.p7 | 12:108648566 | CTAGAGGATAAAGCC[C/T]GAACCAGCCAAGCAC | 23603 |
rs761616687 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681737 | CAAAGAATTGCTATA[C/T]TAATTTTGAAGAATT | 23603 |
rs761633579 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713636 | AAGCTCATCAATTCC[A/G]GGCCCGTCACGTTTC | 23603 |
rs761678353 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724851 | CATTACTGCAGCAAA[C/T]GGGAGGAACTGTATT | 23603 |
rs761699752 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667702 | CCTCTCATCTATATA[A/G]CCAAAAAAATGACAT | 23603 |
rs761716343 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701346 | GGAAGAGTGAGAATT[A/G]TGTTAGAATTATGCA | 23603 |
rs761820647 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689285 | GTTAAAGTCGCACAA[C/T]GCTTTACCCAGCAGG | 23603 |
rs761830938 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703866 | CCCCTTGTTCCTCCT[A/G]GCTCCCAAGATACCA | 23603 |
rs761834366 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701189 | TTATGGCAACAAATC[C/T]GGGATTGACAGCACA | 23603 |
rs761899140 | snp | C/T | 1.65518e-05 | 0.00287674 | intron-variant | CORO1C | GRCh38.p7 | 12:108649046 | GAAATAAAGGCAAAG[C/T]TGCATTAAGTGAAAT | 23603 |
rs761910814 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688620 | TGTTAAAATGGATCA[A/G]TCTAAGCTGGGCACG | 23603 |
rs761985774 | snp | C/G | 1.65102e-05 | 0.00287312 | intron-variant | CORO1C | GRCh38.p7 | 12:108648894 | AAGGAAGAAGAAAGG[C/G]CTGGGATTTTTGAAT | 23603 |
rs762071723 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651713 | AGGTGTGCAATACAC[C/T]CCAGCTATGCTGCTT | 23603 |
rs762093951 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707925 | AAATCAAAACCACAA[A/T]GAGAGACTATTCCAT | 23603 |
rs762188165 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719045 | ACTCTACTACAAAAA[A/G]CTTTTATCAGCTGTA | 23603 |
rs762199233 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721716 | TCAATAATTTCCCAC[C/T]GTTTGATGAAAAAAG | 23603 |
rs762211579 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677856 | AAACCTCGTCTCTAT[G/T]AAAAATACAAAAATT | 23603 |
rs762223106 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716128 | ACGAGACTCTGTCGC[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs762248614 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724017 | CATTAAAAATAGAAA[C/T]CAAGTTTACCAAAGG | 23603 |
rs762257841 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646782 | CATCAAAATGACCAG[A/G]TTTGTGCTGCAAAGG | 23603 |
rs762336048 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662259 | TGCTCTATGTAAACA[G/T]AACATAGAGTGATAT | 23603 |
rs762373375 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695737 | AAGCTGCCTTCATCA[A/G]CCTAGGTTCTATAAG | 23603 |
rs762414197 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655173 | ACACATGTACACAGA[C/G]ATTGAGATGATAGAA | 23603 |
rs762542363 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714910 | GTTGGGGACCACCTA[A/G]AGTCAAACCTAAGCA | 23603 |
rs762555895 | snp | C/T | 1.66205e-05 | 0.00288271 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657304 | CTGGGGAGGGCGTAC[C/T]GGATTCCAGAGAGCC | 23603 |
rs762562943 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685584 | CTAGATTTGGATAGG[A/G]AAAGAAAATTTCCAC | 23603 |
rs762644236 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670396 | CAGGCACAATCTAGA[C/T]CCCAGCACTCTCAAA | 23603 |
rs762648311 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689883 | AGAATGTTAAGTCAC[-/A]ACATGTGCTCAGAAG | 23603 |
rs762661543 | snp | A/C/T | 6.59006e-05 | 0.00573993 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648799 | CTTCTGCCTCCAGCG[A/C/T]GGCCTCTGGCCCCGC | 23603 |
rs762661973 | snp | C/T | 1.65883e-05 | 0.00287991 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647377 | TTCTTGCTCCCATTT[C/T]TTCTGTAGGGGTGGG | 23603 |
rs762663352 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722158 | TTTATCAGTAAGGAA[C/G]CTCCTCTTTAAAAAT | 23603 |
rs762736466 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703967 | CTCACACAGGCATAA[A/G]GTCAGCTTTTAGAAC | 23603 |
rs762778409 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693094 | TGAGCCACCGCGCCC[A/G]GCTAAACCACAGATT | 23603 |
rs762786460 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704454 | TCCAGCCTGGGCGAC[-/AT]AGCAAGATTCCATCT | 23603 |
rs762807416 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682975 | GAGCAATACACAACA[C/T]ATCCAAATGTGCAAC | 23603 |
rs762823882 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658185 | TTGCTTTTCGCCCTG[C/T]GCATTTATTTATTTA | 23603 |
rs762839929 | snp | A/G | 1.65682e-05 | 0.00287817 | intron-variant | CORO1C | GRCh38.p7 | 12:108701359 | TTATGTTAGAATTAT[A/G]CACCAAACTGAAAGC | 23603 |
rs762874530 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687332 | CTGTCCCTACAAATA[C/T]AAAAATTAGTCAGGT | 23603 |
rs762955424 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | CORO1C | GRCh38.p7 | 12:108701117 | AATGGAAGATCAAAT[C/T]ACCTACCTTGTGCAG | 23603 |
rs762968742 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662848 | ATCAAAATTAAAAGC[C/T]TTTGTGCTTCAAAGG | 23603 |
rs762969153 | snp | A/G | 1.65949e-05 | 0.00288048 | intron-variant | CORO1C | GRCh38.p7 | 12:108654418 | ATATTTTTCTGGGGG[A/G]AAGATAATAATAATA | 23603 |
rs762978564 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680604 | TCGGTTCCTCATCTA[G/T]AAAACTAGAATGTTT | 23603 |
rs763008850 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723355 | ATGCTTGACCATTAC[A/G]AAAAGGAATTTAAGT | 23603 |
rs763044940 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699452 | AAGGAAAAAAAAAGT[C/G]TTACATTTATCCCTC | 23603 |
rs763174028 | in-del | -/TGAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664354 | GAGATCTAGACTGGA[-/TGAG]TGAGTGTTTAGGGTT | 23603 |
rs763221290 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658843 | CACATTGTAAATCAT[G/T]TCTGAATGCATATCG | 23603 |
rs763225375 | snp | A/C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688428 | TATTACACATGTACC[A/C/G]CAGCCATGTTCACCT | 23603 |
rs763228992 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717519 | TAGTTAGGAAGTCAC[A/G]GCACTTGTTGTCCAG | 23603 |
rs763265500 | snp | A/G | 3.44768e-05 | 0.00415177 | intron-variant | CORO1C | GRCh38.p7 | 12:108678409 | TCTGAAAGAAGAGAG[A/G]AACAAACCTATTATG | 23603 |
rs763313503 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732133 | TTTAAACCCCAAGCC[C/T]CGCCCCGAATTCGCG | 23603 |
rs763324140 | snp | C/T | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678307 | AACCGCTGGCAATGA[C/T]CTGATCGTTATGTGG | 23603 |
rs763345498 | snp | A/G | 1.656e-05 | 0.00287745 | intron-variant | CORO1C | GRCh38.p7 | 12:108649057 | AAAGTTGCATTAAGT[A/G]AAATATGAGGCTGAC | 23603 |
rs763347508 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694374 | AATGAATGAATGTGA[A/T]TTTTCTAAAGTACTG | 23603 |
rs763419447 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675838 | TGCGAACAATATAGT[C/T]TAGCCAAAAGGACAG | 23603 |
rs763440027 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108717760 | TGTTGACAAGTAAGG[C/T]ATCTGAAAAGAGTAA | 23603 |
rs763441643 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707714 | TCATAGAATGGGAGA[A/C]AACTTTTGCAAACTT | 23603 |
rs763476200 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674319 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCGCGAGA | 23603 |
rs763490835 | snp | A/G | 6.65569e-05 | 0.00576836 | intron-variant | CORO1C | GRCh38.p7 | 12:108652262 | ATACTTGACAATCTC[A/G]ATTCTTTACCTGGCA | 23603 |
rs763496801 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704005 | TTAAATGTGAATGGA[C/T]ATTTGAGGAAGGCCT | 23603 |
rs763577158 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715549 | AACACAACCACCTCT[C/T]TTGGTCCCTGGAGCT | 23603 |
rs763723869 | snp | C/T | 1.7586e-05 | 0.00296524 | intron-variant | CORO1C | GRCh38.p7 | 12:108654450 | ATATATGTGTATGTA[C/T]ACATTTTTTTAAAAA | 23603 |
rs763741115 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665741 | AGCCAGACACACACA[C/T]AGTGCCTCCAGAATG | 23603 |
rs763778114 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723398 | AAGTAAGCAAATAAT[C/G]GTGATTAAACATTTG | 23603 |
rs763815665 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679811 | GTGACTTTAGACAAG[C/T]CATGTAATCTCTCTA | 23603 |
rs763828345 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675181 | CAGTATTTTTAAATG[-/TA]TATATATATATACAT | 23603 |
rs763842145 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658835 | TTCCAGCTCACATTG[C/T]AAATCATGTCTGAAT | 23603 |
rs763848395 | snp | G/T | 1.65228e-05 | 0.00287422 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647394 | TCTGTAGGGGTGGGG[G/T]TGGGACCTTCAGGCT | 23603 |
rs763896814 | snp | C/G | 1.64844e-05 | 0.00287087 | intron-variant | CORO1C | GRCh38.p7 | 12:108701079 | AGGAAAAAGTATGGA[C/G]ACTATCAGAGGGTGT | 23603 |
rs763940504 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683322 | TACTCAGGAGGCTGA[A/G]GCAGGAGAAGTGCTT | 23603 |
rs763942318 | in-del | -/GACA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725056 | ACTTTCCTTAAAATG[-/GACA]GACAGACACACAGAC | 23603 |
rs763979514 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724119 | CAAACTTCACAGTTT[-/A]AATACATGCACAACC | 23603 |
rs763980561 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721571 | AAGACTTTGTGAATA[C/T]GAATTTTTTAAATGA | 23603 |
rs763984479 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679623 | ATATGGCAAATCATC[C/T]CAACACTGGAGCAGG | 23603 |
rs763993831 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685389 | AACAAATAATAACAA[A/T]GGCTAACACTTTTTA | 23603 |
rs764013167 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666433 | GGAAAGAGCTTGGGG[A/G]TTGGGGGCGGTCTGT | 23603 |
rs764073423 | snp | C/T | 3.40049e-05 | 0.00412326 | intron-variant | CORO1C | GRCh38.p7 | 12:108647551 | AAAAGGAGGCAGTGA[C/T]TAAAATGCAGTAAAC | 23603 |
rs764085054 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665214 | TCTCTAGCTTCTCCC[A/C]ATCATCTTTTCCTGG | 23603 |
rs764153352 | snp | A/G | | | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701149 | GGGAGGACAAGGAAC[A/G]CTCCTCCCCCACTTG | 23603 |
rs764230330 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687381 | AGTCCCAGCTACTTG[A/G]GAGGCTGAGGTGGGA | 23603 |
rs764241979 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648806 | CTCCAGCGCGGCCTC[C/T]GGCCCCGCTGTGTCA | 23603 |
rs764348183 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718974 | GGAAGTGAAGACAAA[C/T]AAACACGGCCCACTT | 23603 |
rs764355035 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650003 | ACTGGGCAGGAGTCC[A/G]TTGAAGACAACCTGG | 23603 |
rs764436209 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717579 | AGATGATGGAGCCAA[A/G]AGACTTGAAGTCAAC | 23603 |
rs764461612 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696153 | TGGCCAGAGCAGCAT[A/T]CTTGTCCCAGGTAGT | 23603 |
rs764487148 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661910 | ATACTCTTCACCATG[G/T]TTTCCTAATAATCTG | 23603 |
rs764528013 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647591 | CACTGTTCAAAACTT[G/T]TAAGATATAAAATGT | 23603 |
rs764537573 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682440 | GAAATGCACTATTAG[A/C]GATTAATGTCACTAT | 23603 |
rs764575802 | in-del | -/ATTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725804 | GTGCTAAGTGAATTT[-/ATTT]ATTTATTTATTTATT | 23603 |
rs764648546 | snp | A/C | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648731 | TTTGCCTGGAATGTA[A/C]CCGTGCTTCAAGGAG | 23603 |
rs764648940 | snp | C/G | 3.29989e-05 | 0.00406182 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662122 | CCACAGGTTCAGTCA[C/G]GGAAAGGGTGAGTCC | 23603 |
rs764687359 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660229 | GGCCGAGGCGGGCAG[A/C]TCACCTGAGGTCAGG | 23603 |
rs764703461 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694552 | AAAACATCACTTTTA[A/G]TCCCATCAATGTTAA | 23603 |
rs764731655 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684156 | GCAGAGAACTCACAG[A/C]GAAGAAAATCTGAAG | 23603 |
rs764819554 | in-del | -/AG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651926 | CTACTTGGAAGGCTA[-/AG]AGGCAGGAGAATTGC | 23603 |
rs764928696 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690163 | GCAGACCAAAAAGAC[A/G]GGTGCACACAATATA | 23603 |
rs764928840 | snp | A/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703852 | AGTGGGGCCTCCAGC[A/C]CCTTGTTCCTCCTGG | 23603 |
rs764978826 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663587 | CCAGACATAGAAGAC[C/T]GCATATTGCAGGATT | 23603 |
rs765047650 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648666 | CACTTCTTGTTTGCA[C/G]TGGGCTTGCTATCCA | 23603 |
rs765066547 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679056 | GCAGAGGTTGCAGTG[A/G]GCCGAGATCGTGCCA | 23603 |
rs765092806 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710291 | ACCAAGTTTTCCAGG[C/T]GATACTGAAGGCCAA | 23603 |
rs765120641 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691060 | CCCTCCTTGGATGGT[A/G]GAGATGATAAATAGA | 23603 |
rs765138152 | snp | A/G | 3.44774e-05 | 0.00415181 | intron-variant | CORO1C | GRCh38.p7 | 12:108678410 | CTGAAAGAAGAGAGA[A/G]ACAAACCTATTATGT | 23603 |
rs765182790 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722078 | ACTTCACATGCCTCT[C/G]CTCAACTTTCCCCTT | 23603 |
rs765187386 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717510 | CAGGGAAGCTAGTTA[-/G]GAAGTCACGGCACTT | 23603 |
rs765221072 | snp | C/G | 1.65195e-05 | 0.00287393 | intron-variant | CORO1C | GRCh38.p7 | 12:108701337 | GTCTGCAAAGGAAGA[C/G]TGAGAATTATGTTAG | 23603 |
rs765274212 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701192 | TGGCAACAAATCTGG[C/G]ATTGACAGCACAAAA | 23603 |
rs765288886 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711418 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 23603 |
rs765399164 | snp | C/T | 3.33322e-05 | 0.00408228 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658694 | GAAAGCTCACACTCA[C/T]TCAAGTGCTCCAACT | 23603 |
rs765400051 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730360 | AAAGGATGCCAGGGC[C/T]AGCGCCTCCCTCCAA | 23603 |
rs765414677 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660238 | GGGCAGATCACCTGA[A/G]GTCAGGAGTTGGAGA | 23603 |
rs765417414 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699294 | TAAGTGAAACTCAGT[G/T]TCTCATGGTCTGTAA | 23603 |
rs765431915 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647256 | GTTCTTACTGGAATG[C/T]GGCCTATCGCTGGTT | 23603 |
rs765483964 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665485 | CCTGCTCTTGAGAAG[C/T]TGATGGTCTAACAGA | 23603 |
rs765571408 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704963 | TCATTAAATGATCAA[C/T]TGGTGATGGGATGGT | 23603 |
rs765584697 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713587 | GAAGCCTCCAGGCTC[A/G]GGCCTCACAGAGCTA | 23603 |
rs765613339 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717329 | AGAACCCGGATCACA[A/G]AGGGCTTTCTAGGCC | 23603 |
rs765637670 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674301 | GGCACGGTGGCTCAC[A/G]CCTTTGGGAGGCCAA | 23603 |
rs765725536 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660066 | ACGGGAAGGACATCC[C/T]AGAGGTGGATTCTTG | 23603 |
rs765734485 | snp | A/G/T | 3.29474e-05 | 0.00405867 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648813 | GCGGCCTCTGGCCCC[A/G/T]CTGTGTCAGGATACA | 23603 |
rs765764089 | snp | A/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732044 | AAGCCCCGCCCCGTC[A/T]TCCAGAAGCCCCGCC | 23603 |
rs765805711 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706502 | ACTATTTCTGTGTGC[C/T]GAAGACATGATCTTA | 23603 |
rs765842597 | snp | C/T | 3.30863e-05 | 0.00406719 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678295 | TGCAGTCCTCTGAAC[C/T]GCTGGCAATGACCTG | 23603 |
rs765871173 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706053 | TTAGCCAGGCATGGT[C/G]GTGGGCACCTGTAAT | 23603 |
rs765879192 | in-del | -/AGTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665562 | TGGTGTGATACAGAC[-/AGTT]AGTTAGAGAGTGAGC | 23603 |
rs765920531 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678706 | TGTAAATTAAAAGGA[A/T]GTTCCATGGCTTAAA | 23603 |
rs765951107 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667940 | CACGTGCTAATTTTA[A/C]AGTACAATTAGTTAA | 23603 |
rs765964173 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725028 | TCCTAAAAAAATCCA[C/T]CTTTTGCCAGGAACT | 23603 |
rs765996119 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701491 | TAGCAGCACATACCC[A/G]GAGACAACTGCAAAA | 23603 |
rs766020934 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653856 | TTCCAAGTCCATGGT[C/G]TGTGGTACTAAGTAT | 23603 |
rs766063298 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713938 | ACACTTTATAAATAT[A/G]AGTAAAAATGGAAAA | 23603 |
rs766070984 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682327 | TATCCAGCTACACAT[A/C]TTTTAAAAAAATAAT | 23603 |
rs766076018 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702530 | TGTAATTTTCCTATG[G/T]GCTACTGCAGGACAT | 23603 |
rs766158265 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659668 | TTAAATGACTGTTTA[A/G]GGCACTCAACAAAAA | 23603 |
rs766161190 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727309 | ATGAGGAAGTTTTCA[C/T]GGAGGAAAAACCTCA | 23603 |
rs766170351 | snp | A/G | 4.98227e-05 | 0.00499088 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657305 | TGGGGAGGGCGTACC[A/G]GATTCCAGAGAGCCA | 23603 |
rs766204624 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703821 | CAGATGCCTCACTGA[C/T]AGCCTGGTTCTATAC | 23603 |
rs766228504 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730265 | CATTACGGCCAAATA[C/T]AGGATGTGTTTCTAA | 23603 |
rs766259409 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676492 | ATTCTGGCATCAGAG[C/T]TAGGCGCAGTGGCTC | 23603 |
rs766270213 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689517 | AGACTGCTTTCTACA[C/T]GGTTTCCCTTATCTA | 23603 |
rs766295617 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690994 | CAGGGCTAACCCTTC[C/G]CATTGCAGCTCTGCA | 23603 |
rs766322379 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651926 | GCTACTTGGAAGGCT[A/G]AGGCAGGAGAATTGC | 23603 |
rs766386049 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663450 | CCATCTATCGATAAA[C/T]GGCTGAACAAAATGC | 23603 |
rs766396883 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647193 | TTCTGATAAAAAGCT[C/T]AGCTTTTAAATCACG | 23603 |
rs766404125 | snp | G/T | 1.66402e-05 | 0.00288441 | intron-variant | CORO1C | GRCh38.p7 | 12:108654432 | GGAAGATAATAATAA[G/T]ACATATATGTGTATG | 23603 |
rs766455388 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678089 | TTTAAGGGCTTCTTG[A/G]AAGGATTATCTGTAA | 23603 |
rs766457982 | in-del | -/AAG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722918 | GTCTTAGGGAGAAAA[-/AAG]AAGACTTCCAACTTA | 23603 |
rs766548619 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710146 | CTAGAATGGTTTTTA[C/T]TATAATAAAAATTGA | 23603 |
rs766574976 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658852 | AATCATGTCTGAATG[C/T]ATATCGTCCAAGTTT | 23603 |
rs766623022 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715081 | AAGATAAAATTCCTA[A/C]AACTGGGCTGGGTGT | 23603 |
rs766655921 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684511 | GGCAAAAGCAGAAGC[A/C]ATTTCACTGTCCTTC | 23603 |
rs766745376 | snp | C/T | | | intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108730258 | CAGCCTACATTACGG[C/T]CAAATATAGGATGTG | 23603 |
rs766800520 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657168 | CGAGGATAAGAACTT[C/T]ACATCCAATCTAAGA | 23603 |
rs766813780 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704656 | CATCTCTAAGCGGAG[C/T]TTGAAGGGCAGTGTG | 23603 |
rs766851095 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685987 | ACAAAAGCACAACAA[C/T]ATATTTCACCAAATC | 23603 |
rs766886565 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108648255 | ATATTTTATTTCTAC[C/T]CAAATCAGAGAAGGG | 23603 |
rs766915431 | snp | A/G | 1.65187e-05 | 0.00287386 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678329 | GTTATGTGGGCACCA[A/G]TCTATGTCCAGCACT | 23603 |
rs766919638 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711679 | GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 23603 |
rs766927952 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692129 | ATAATTTGGAAGTCA[C/T]TGTTCTGCACCTGGT | 23603 |
rs766965975 | snp | A/T | 1.65573e-05 | 0.00287721 | intron-variant | CORO1C | GRCh38.p7 | 12:108649059 | AGTTGCATTAAGTGA[A/T]ATATGAGGCTGACTA | 23603 |
rs767008159 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706284 | TAGAAGGGAATTTCC[A/T]CAACCTGATAATGGG | 23603 |
rs767060841 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658247 | GACAGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 23603 |
rs767108291 | snp | A/G | 0.000217244 | 0.0104199 | intron-variant | CORO1C | GRCh38.p7 | 12:108652256 | CCTAGAATACTTGAC[A/G]ATCTCGATTCTTTAC | 23603 |
rs767121876 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679734 | AACGTTAACGTGTAA[A/G]GACCACAGGCTCTGG | 23603 |
rs767154259 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680699 | TCTGCCCCAGCACTT[A/G]AAGTACTCAATAAAC | 23603 |
rs767199614 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712710 | AATTTGGCCGGGCAC[A/G]TTGGCTCACGCCTGC | 23603 |
rs767202517 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672303 | TGTAACAGCTATGTG[A/G]TCTTGAAAATACAGA | 23603 |
rs767246036 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693289 | TGTAGAACAGAGGAA[A/T]GATCCCACCCTACCA | 23603 |
rs767300014 | snp | A/C/G/T | 0.000115752 | 0.00760695 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647390 | TTTTTCTGTAGGGGT[A/C/G/T]GGGGTGGGACCTTCA | 23603 |
rs767321878 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657326 | CAGAGAGCCAGCTGC[C/T]GCTCGCTCATGCGGC | 23603 |
rs767344730 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659431 | TATACTATAGAGAAC[A/G]TATATAAACAAAAGG | 23603 |
rs767357820 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650045 | CTCTAACGCATCAGG[A/G]GAACAAAAGCTGAGT | 23603 |
rs767422590 | snp | A/G | 8.3316e-05 | 0.00645376 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658689 | AAGCAGAAAGCTCAC[A/G]CTCACTCAAGTGCTC | 23603 |
rs767528909 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108662354 | TGTTTTTTGTTTTTC[A/G]TTTTTGAGACGGAGT | 23603 |
rs767554019 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666577 | GATGGCCTGCTCGGT[C/T]TGGACTGATGTTCCT | 23603 |
rs767575634 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694778 | ATGTATATAGATATT[A/G]TATTTCTACGTAGAT | 23603 |
rs767579398 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660571 | CTGCCTTCTTCCCTA[C/T]AGGCAAACAGGTAAC | 23603 |
rs767602265 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683487 | AAAATCAACTAAACT[A/G]GATAGATCAGGAAAA | 23603 |
rs767607945 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719078 | TGGTAAAACTGTAGC[C/T]CTAACTCTCCCAAAT | 23603 |
rs767674589 | snp | A/C | 1.65877e-05 | 0.00287986 | intron-variant | CORO1C | GRCh38.p7 | 12:108662017 | GGGAGGACCGCTGAG[A/C]TCAGCTCCCACCTGC | 23603 |
rs767688304 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648701 | GTTCTTCTTGACCAC[C/T]TTGAGATCCCTGTTT | 23603 |
rs767708215 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646058 | GTTGTGCGGAGGGAC[-/AT]GTTTGTATGCATTAA | 23603 |
rs767811217 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692462 | GGCAGACATGCAGCC[A/C]ATGCAAATCCAGCAG | 23603 |
rs767812361 | in-del | -/ATTT | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658191 | TCGCCCTGCGCATTT[-/ATTT]ATTTATTTATTTATT | 23603 |
rs767826029 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712559 | AGCCTGAACAACAAG[C/T]GAAACTGTCTCAAAA | 23603 |
rs767834067 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727808 | AGAAAATGAAAGGAC[A/G]TGTCAGAATCCAAGA | 23603 |
rs767838538 | snp | C/T | 4.98418e-05 | 0.00499183 | intron-variant | CORO1C | GRCh38.p7 | 12:108652440 | AAACCAGAGACAAGT[C/T]TGTGTCTGATTGTTA | 23603 |
rs767848217 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714965 | GCAGTGAGCGCATTG[C/T]AGAGCGTAATGTGAC | 23603 |
rs767868578 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685607 | ATTTCCACTATGCCA[C/T]GGGTTGTAAAAAAAA | 23603 |
rs767881620 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707998 | GGGTTGATGAGAATA[C/T]AGACAAATCAGAACC | 23603 |
rs767889142 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646010 | TGTGCTTTGACGCAG[A/C]CTTGGTGAGAGATGG | 23603 |
rs767967904 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669206 | TCAATGCCCACAAAA[C/T]TAACAAATCAATGCT | 23603 |
rs767991524 | in-del | -/CT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665819 | GATGTGACTGAATTC[-/CT]GATTCAGTCACATAG | 23603 |
rs768030410 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728714 | AAGGATCTGAACTAG[A/G]GCAAAGAAAACCCAG | 23603 |
rs768077215 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673613 | TTCATGGCTAGAGAG[G/T]AGAAGTCAATGCCTG | 23603 |
rs768088134 | snp | A/G | 8.23635e-05 | 0.00641677 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658858 | GTCTGAATGCATATC[A/G]TCCAAGTTTATAAGG | 23603 |
rs768095116 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714183 | ATCACGAAGTCAAGG[G/T]ATTGAAACCATCCTG | 23603 |
rs768167585 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658768 | TTTCCTGGGATCAAT[A/G]ACTCTCACTTTCTTG | 23603 |
rs768179724 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658186 | TGCTTTTCGCCCTGC[A/G]CATTTATTTATTTAT | 23603 |
rs768247227 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717939 | AAATGAAAACTAGGC[C/T]GGGCACAATGGCTCA | 23603 |
rs768256829 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687848 | ATGATATTGCTTAGC[C/T]GTAAGGGCACTTCCT | 23603 |
rs768292042 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660987 | CTTTTTACTGGTGAG[A/G]GGAAAGACCTTTAAA | 23603 |
rs768335140 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717097 | TAACTGAGTCAATAA[C/T]CGGGGAACAGAAGCA | 23603 |
rs768370170 | snp | C/T | 0.000166597 | 0.00912529 | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702907 | GTTCCTTAGCCCAGC[C/T]GTTATTGCCAGACTT | 23603 |
rs768405075 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729517 | ACCAAATCTTTGTCC[A/G]ATCCTCAGTACACAC | 23603 |
rs768422673 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726180 | AAACATAATCTGGGA[A/G]GCCGAGGCGGGCGGA | 23603 |
rs768451656 | snp | G/T | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644789 | GTATTCCTCTCATCT[G/T]AACTACATGGAATTA | 23603 |
rs768466513 | in-del | -/GTAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651190 | TTTTATTTGGAAGAC[-/GTAA]GTATCAATTCTTTAA | 23603 |
rs768486704 | snp | A/G | 9.89821e-05 | 0.00703429 | missense, utr-variant-5-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701320 | ACCACTCGCCTCATC[A/G]TGTCTGCAAAGGAAG | 23603 |
rs768501848 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706884 | CTACCATGCCTAGCC[A/G]TATTTTTATAAAATC | 23603 |
rs768508579 | in-del | -/AT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686274 | AAAGACATCCACCAC[-/AT]GTCATGGTGACAACA | 23603 |
rs768511383 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648649 | GGATGCTGATCAGGT[C/T]GCACTTCTTGTTTGC | 23603 |
rs768519524 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712669 | CACCCAAAGCAAATA[C/T]AGGAGGTACTCTGAT | 23603 |
rs768565062 | in-del | -/TA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675182 | GTATTTTTAAATGTA[-/TA]TATATATATATACAT | 23603 |
rs768610261 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713570 | CAAATAAGATCTACC[A/C]AGAAGCCTCCAGGCT | 23603 |
rs768635804 | snp | A/C | 1.66685e-05 | 0.00288686 | intron-variant | CORO1C | GRCh38.p7 | 12:108661983 | CCCCACTCAGAGAGC[A/C]ACAAGAGTGGAAGAC | 23603 |
rs768665283 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724651 | CCAAAATAATATATC[A/C]TTTAAAAGATGGTGA | 23603 |
rs768680423 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681644 | GAAAAAAGCAAACAA[A/G]AGGCACTGCAGACAA | 23603 |
rs768684919 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723735 | AACCTTTGCTAATCC[A/T]AAGTGGTTTTCATTA | 23603 |
rs768709679 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670737 | AGAAAAAAAGAAAAT[-/AA]GACACAGAATAAGAT | 23603 |
rs768721967 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656335 | GTCCGGGAGGGAGGT[-/G]GGGGGGTCAGCCCCC | 23603 |
rs768798067 | snp | C/T | | | intron-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108653078 | GGCAGAGAGGAGATA[C/T]ACATATATGTAAGAA | 23603 |
rs768822081 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | CORO1C | GRCh38.p7 | 12:108703041 | TCAAGCGTGAGTTAG[A/G]TAAGACAGCTTCCAT | 23603 |
rs768831209 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651611 | CACTTTTCCATCCCC[A/G]AGCCAGGCTCTCCCT | 23603 |
rs768927381 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663052 | AGACATATAAATGGC[A/G]AAAAAGCACATGAAA | 23603 |
rs768936123 | snp | G/T | 1.65403e-05 | 0.00287574 | intron-variant | CORO1C | GRCh38.p7 | 12:108649031 | AGAATCTTCAGAGGG[G/T]AAATAAAGGCAAAGT | 23603 |
rs768976029 | snp | C/T | 1.69186e-05 | 0.00290844 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678385 | GGTAAGATTTGTCAA[C/T]TCGACCAGTCTGAAA | 23603 |
rs769020479 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690778 | TGGAACCCAAGATGA[C/G]GTAGAATCTAGTTAA | 23603 |
rs769043002 | in-del | -/AAGT | 0.004137 | 0.0452922 | frameshift-variant, intron-variant | CORO1C | GRCh38.p7 | 12:108702856 | CATGTAGCCGGGCTG[-/AAGT]AAGAGACCCTTGGCA | 23603 |
rs769060514 | snp | C/G | 4.95094e-05 | 0.00497517 | intron-variant | CORO1C | GRCh38.p7 | 12:108648888 | GTGGGTAAGGAAGAA[C/G]AAAGGCCTGGGATTT | 23603 |
rs769086762 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708898 | GCTGGGACCACAAGC[A/G]TACGCCACCACACCA | 23603 |
rs769089003 | snp | C/T | 3.29821e-05 | 0.00406078 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657362 | CCAGTGGTGAAGACA[C/T]TGCCATCGGCCAGGA | 23603 |
rs769092433 | snp | C/T | 3.37109e-05 | 0.0041054 | intron-variant | CORO1C | GRCh38.p7 | 12:108657277 | AAGCTCAAGTGAAAG[C/T]AAGTGGAAAGCCTGG | 23603 |
rs769107330 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677761 | CTCACAGAAAAGACT[G/T]TAATCCCAGCACTTT | 23603 |
rs769155625 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709855 | CTGCTTGCTCATTAG[C/G]TCTTTCAAGTACAAG | 23603 |
rs769156833 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681253 | AATAGACAAACCAAA[A/C]GGAGAGAATTAAAAG | 23603 |
rs769194498 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675844 | CAATATAGTCTAGCC[A/G]AAAGGACAGAACCTG | 23603 |
rs769283384 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650494 | CAAAAACATTTTTAA[A/G]GACTGATTTAATGAA | 23603 |
rs769308103 | in-del | -/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108730995 | GTCCCCAGGCCTGGA[-/G]CCCCCGGGCTCTACG | 23603 |
rs769323171 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728589 | CTTTAAACGGGTGAA[C/T]TGTACAGTATGTCTC | 23603 |
rs769325074 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670218 | GCCACACGACCTGCA[G/T]GTGATCAGCCTCGGG | 23603 |
rs769336505 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654451 | TATATGTGTATGTAT[A/G]CATTTTTTTAAAAAT | 23603 |
rs769349922 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697683 | AGTCCCCATCATATT[A/T]CTTCTTCGAGGCTGT | 23603 |
rs769358701 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729729 | TTAAATCATCTGAAA[C/T]GTATAGAACCAAGTC | 23603 |
rs769389355 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698761 | AGAGAAACAGAGGAG[C/T]GGAAGGATAAAGAGA | 23603 |
rs769399983 | snp | A/G | 0.000282207 | 0.0118753 | utr-variant-5-prime, intron-variant | CORO1C | GRCh38.p7 | 12:108702985 | GATGGCAAATGATTC[A/G]TGGCCAGGGTCCTTC | 23603 |
rs769420738 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687943 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 23603 |
rs769494370 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685578 | ACCATACTAGATTTG[A/G]ATAGGGAAAGAAAAT | 23603 |
rs769507594 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662076 | TGCCAAGCCACGATG[C/T]CGACTCTCTTTGAGT | 23603 |
rs769625321 | snp | A/G | 3.34124e-05 | 0.00408719 | intron-variant | CORO1C | GRCh38.p7 | 12:108657295 | GTGGAAAGCCTGGGG[A/G]GGGCGTACCGGATTC | 23603 |
rs769654931 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723318 | AAGAATGAAAGGAAT[C/T]AGAATCTTTAACTAG | 23603 |
rs769683660 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708698 | AACTCCTGACCTCAG[A/G]TGATCTGCCCACCTT | 23603 |
rs769696515 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666400 | AAAGAGGGGGTGGTG[C/T]TCTCTACGGTGGACT | 23603 |
rs769711043 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704404 | TTGAACCTGGTAGGC[A/G]GAGGCTTCAGTGAGC | 23603 |
rs769722285 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667094 | AAAAAAAAAAGAGCC[C/T]ACCATATTTTCATGA | 23603 |
rs769765678 | snp | A/G | 3.29853e-05 | 0.00406098 | intron-variant | CORO1C | GRCh38.p7 | 12:108648869 | CAAGAGACATTTGGC[A/G]CCCGTGGGTAAGGAA | 23603 |
rs769770720 | snp | C/T | 9.88452e-05 | 0.00702942 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648788 | TTCGAACCACTCTTC[C/T]GCCTCCAGCGCGGCC | 23603 |
rs769792981 | snp | A/C/T | 4.96613e-05 | 0.00498283 | intron-variant | CORO1C | GRCh38.p7 | 12:108649052 | AAGGCAAAGTTGCAT[A/C/T]AAGTGAAATATGAGG | 23603 |
rs769794436 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678180 | TTCTGCTTTTCAAGC[C/T]TCTATACATACACAC | 23603 |
rs769854592 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724364 | TACTATAAATTCACA[C/T]AACTAACTATAAAAA | 23603 |
rs769880658 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723353 | GAATGCTTGACCATT[A/G]CGAAAAGGAATTTAA | 23603 |
rs769887291 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649721 | TTATGATGACCCTGA[C/T]AAGGTCAAGCCAATT | 23603 |
rs769898365 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705695 | GACCAATATCTCTTA[C/T]GAATACAGATGCAAA | 23603 |
rs769902538 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691829 | AAGGCTGCCTGCTCA[A/T]CTCCAGGGGAGGGGG | 23603 |
rs769937619 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650113 | CTCTTTAAAAGGAAG[C/G]TTGTGTCAAATGTGC | 23603 |
rs769941523 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667310 | TTACCACAGTAAGGA[A/C]AGATCTGATCTCTGT | 23603 |
rs769958585 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713440 | CCCATCATTATTAAT[C/T]CAGGTAACAGGTAAG | 23603 |
rs769978465 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720783 | CCGCCTCAGCCTCCT[A/G]AAGTGCTGGGATTAC | 23603 |
rs770047163 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712438 | AATCAGGTGGGCGTG[G/T]TTGCAGGTGCCTGTA | 23603 |
rs770089022 | in-del | -/CA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672628 | CATTTTATTGCACTT[-/CA]CAGATATTGTGGTGG | 23603 |
rs770102962 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652380 | TGGACGTACGGGGAT[G/T]CATCCGTGATCTCAA | 23603 |
rs770143344 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707639 | ATTAGAAAAACTGGA[A/T]TCCATCAAAATTTAT | 23603 |
rs770145391 | snp | A/G | 1.71784e-05 | 0.00293069 | intron-variant | CORO1C | GRCh38.p7 | 12:108678404 | ACCAGTCTGAAAGAA[A/G]AGAGAAACAAACCTA | 23603 |
rs770201215 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688376 | ACGTCTCAATAAAGT[C/T]CTGTGCTGGGGTGTG | 23603 |
rs770243680 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647276 | TATCGCTGGTTGACA[A/G]ATCTGAAATGGAATG | 23603 |
rs770246741 | in-del | -/AG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702784 | GAATTTATTTTTGCC[-/AG]AGTCTCTTACCCTTC | 23603 |
rs770255422 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651530 | GGTTTCTCTATTTTA[C/G]GACCAGTGGGGCCCC | 23603 |
rs770280880 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719632 | TGGTGCTGGGCAGGG[C/T]ACACCTAGAGGTCCA | 23603 |
rs770313966 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675666 | ATCTTATAAAATTTT[A/G]CCAGCTAAAAATTGA | 23603 |
rs770362160 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646540 | AATATGATCCTAGGT[A/G]TGTAACAAACTGCAG | 23603 |
rs770444434 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant, missense | CORO1C | GRCh38.p7 | 12:108657452 | AGGCACATGCCACAC[A/G]TTAAACTGCAAGAAG | 23603 |
rs770474944 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708619 | GGCGCCTGCCACCAC[A/G]CCCAGCTAATTTCTG | 23603 |
rs770517447 | in-del | -/ATCA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701083 | AAAAGTATGGAGACT[-/ATCA]GAGGGTGTCTACCAG | 23603 |
rs770533178 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697446 | GGAGCCTAACACACA[A/T]CTAAACATCATTTCT | 23603 |
rs770558785 | in-del | -/AAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712571 | AAGCGAAACTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 23603 |
rs770610130 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711390 | ACAAAATACAAAAGA[A/T]AGAAAAGGGCCGGGC | 23603 |
rs770619286 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695955 | AAATGAGTTGAAAAA[C/T]TGTTCACAGACATAA | 23603 |
rs770662877 | snp | A/G | 3.29951e-05 | 0.00406159 | intron-variant | CORO1C | GRCh38.p7 | 12:108648877 | ATTTGGCACCCGTGG[A/G]TAAGGAAGAAGAAAG | 23603 |
rs770684089 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661574 | TTCTCTACAGTATAC[A/G]TGTACTAATTGTATA | 23603 |
rs770727330 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685383 | TATCAAAACAAATAA[C/T]AACAATGGCTAACAC | 23603 |
rs770766039 | snp | C/T | 1.65737e-05 | 0.00287864 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647383 | CTCCCATTTTTTCTG[C/T]AGGGGTGGGGGTGGG | 23603 |
rs770901886 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721936 | AAAAAAAAAGATCAG[A/G]AAGTATTTTGAAAAA | 23603 |
rs770920855 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676771 | GTGAGACTCCATCCC[-/A]AAAAAAAAAAAAAAA | 23603 |
rs770924128 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691769 | GCTGCTGTGGACATA[C/T]CAGTGAACTGCAGCA | 23603 |
rs770943066 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703530 | ACTGACTGAAGTGTG[A/G]GTGTCCTCTACTCAG | 23603 |
rs770943724 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704298 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 23603 |
rs771028691 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657695 | TGCCAACCCAAGTCT[A/G]TGCACTGTGAAAATA | 23603 |
rs771031880 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | CORO1C | GRCh38.p7 | 12:108654300 | AACATCAAAATTACT[A/G]TTTACCTTTCCACAT | 23603 |
rs771033711 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715405 | TGAGAATATATAAGG[A/T]CTTCGAAATCATCTC | 23603 |
rs771051695 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108677785 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 23603 |
rs771085153 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724271 | AAAGGCTAAGCAAAT[A/G]GAACTGCTGCACTGG | 23603 |
rs771107347 | in-del | -/GA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685672 | GCCATCAGAAACACA[-/GA]GTTAATAAAAAATGA | 23603 |
rs771118601 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679316 | TTAGACCTCACCCAT[C/T]AGCCAGTTCCACATC | 23603 |
rs771125117 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | CORO1C | GRCh38.p7 | 12:108661997 | CCACAAGAGTGGAAG[A/G]CAAGGGGAGGACCGC | 23603 |
rs771129135 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711273 | TACTCGGGGAGCTGA[A/G]GTGGGAGGACTGCTT | 23603 |
rs771155535 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680242 | CAAGCAGGTTTGTGG[A/G]GTCACAGTCTCTGGA | 23603 |
rs771253347 | in-del | -/TGTACT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655448 | GAGCCGAAGCTGGAC[-/TGTACT]GCTGCCATCTCGACT | 23603 |
rs771282574 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727443 | CTAGAGATGAAGACA[C/T]TGGAAGGGGAATAGT | 23603 |
rs771285904 | in-del | -/TTTTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652042 | AAAAAAAAAGTGAGA[-/TTTTT]TTTTTTTCTTTTCTT | 23603 |
rs771296011 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651028 | CAGTGGCACCATCTC[A/G]GCTCACTCCGCCTCC | 23603 |
rs771333322 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701603 | GAAAGATTAAGGGAA[A/T]GAATTAAAGAAAATT | 23603 |
rs771337477 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699159 | CTAGTTCCCATAATG[C/T]TGGTTAAAGAATGAA | 23603 |
rs771361026 | snp | A/G | 1.64923e-05 | 0.00287156 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652400 | CGTGATCTCAAAATA[A/G]CGAATACTGCTGTCA | 23603 |
rs771369518 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701262 | ATAGCACTGGTCATT[C/T]TTCACCGCTTGCCCA | 23603 |
rs771374067 | snp | C/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731871 | TCTGCAAGGCCACGT[C/G]CCCTGGCTCCTCAAA | 23603 |
rs771404084 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666256 | AGCTGGCTCAGGAGC[G/T]GCTAGGGAAAAAGCA | 23603 |
rs771411354 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733266 | AGCATGGACCTCCCG[A/G]GCTCAAGTAATCCTC | 23603 |
rs771485925 | snp | A/G | 0.000115307 | 0.00759211 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701144 | GCAGAGGGAGGACAA[A/G]GAACGCTCCTCCCCC | 23603 |
rs771494047 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649620 | TACTGGAAGAAGGGA[A/G]CAAAGAGCTCTGTAA | 23603 |
rs771503981 | in-del | -/GTTTTTTT/TTTTTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652041 | AAAAAAAAAAGTGAG[-/GTTTTTTT/TTTTTT]ATTTTTTTCTTTTCT | 23603 |
rs771504614 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661161 | TCAAGATACAGAATA[C/T]TTCCATCACCCCACA | 23603 |
rs771505016 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663434 | GAAACAACCCAAATA[G/T]CCATCTATCGATAAA | 23603 |
rs771517007 | snp | C/G | 4.96356e-05 | 0.0049815 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658928 | TCACAGCCTAAAACA[C/G]GCAAAACCATCAGAG | 23603 |
rs771528094 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688200 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCCAGTA | 23603 |
rs771540054 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659979 | CAAGGGTCTGCCCCA[C/T]GCCTCCAGGCCCCTT | 23603 |
rs771574270 | snp | G/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701151 | GAGGACAAGGAACGC[G/T]CCTCCCCCACTTGCC | 23603 |
rs771582232 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693986 | AGATCAAGCACAGTT[A/G]TTGAAGCTTCTTAAA | 23603 |
rs771618293 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700452 | CCCACCTTGGAGCAG[A/G]CTTTCTGGGAGGATA | 23603 |
rs771618428 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687013 | ACCGTGGCAGAAACC[A/G]TCCCAGATACAAGCA | 23603 |
rs771648298 | snp | A/G | 5.07035e-05 | 0.0050348 | intron-variant | CORO1C | GRCh38.p7 | 12:108647541 | AGAAAACAAAAAAAG[A/G]AGGCAGTGATTAAAA | 23603 |
rs771740144 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674239 | TACCACTGATAGTGA[C/T]TCCCCTGATGGATCT | 23603 |
rs771759636 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707415 | GATTTTCAACAAGAG[C/T]GCCAAGACAATTCAG | 23603 |
rs771772469 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681808 | AAGGTATAGCAAAAC[A/G]ACAGTGAGCAAATAA | 23603 |
rs771789247 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720334 | TACCAAAATGTTGTG[-/T]TATCCTGCTTTTTAT | 23603 |
rs771854527 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714343 | GCAGTGAGCCAAGAT[C/T]GCGCCACTGCACTCC | 23603 |
rs771908109 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695555 | GGTATGAAGAAGCAA[C/T]TAAGAGAACCCAATG | 23603 |
rs771962151 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645160 | GCAAGTGTTTTGACA[C/G]AACACTATGGCCACT | 23603 |
rs771981910 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726986 | AAGGGAGTTACCCCA[C/T]TCATGTTATTTTAAC | 23603 |
rs771987972 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685411 | ACTTTTTAAGTACTT[-/A]AAATTACAAGCTAGG | 23603 |
rs771989893 | snp | C/T | 6.58946e-05 | 0.0057396 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658817 | ATCAGACTGCCATTC[C/T]GGTTCCAGCTCACAT | 23603 |
rs772048316 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703331 | ATTAGACAAAGGATA[C/T]GAAGAATTTACAAAA | 23603 |
rs772085689 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713781 | TTTCCAACAATCAAT[A/C]CCGAATCATATATAC | 23603 |
rs772110134 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683874 | AGAGAACAGAAAAAA[G/T]AAAAGTGCCACTGAA | 23603 |
rs772176488 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728282 | CCCAAATGTTCATCA[A/C]CTGATGAATGGATAA | 23603 |
rs772244400 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691694 | GGCTGACAGCCACAG[C/T]GCTCTGATGGCCATA | 23603 |
rs772280893 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674216 | AATACATTTCATAAG[C/G]CTACAGCTACCACTG | 23603 |
rs772318190 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722626 | ACAATGCTGAATCAA[C/T]ACAATAGATAGAAAT | 23603 |
rs772336089 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690859 | GTAAATGCAATATGG[A/C]AAATTAAAGCATTCA | 23603 |
rs772387444 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704255 | AGCTGAGACGGATCA[C/T]GAGGTCAGGCGATCA | 23603 |
rs772397874 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653758 | TTCAAGCCCAGAGCC[C/T]TAGCACTGAACCCCA | 23603 |
rs772398197 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670018 | ATGCCAATAAAAGGG[C/T]GACATTGAGGATTCT | 23603 |
rs772426286 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727185 | ATTCTGCCTTGTATG[A/G]AAAGGCACCTTTCAG | 23603 |
rs772502968 | snp | C/T | 3.38049e-05 | 0.00411112 | intron-variant | CORO1C | GRCh38.p7 | 12:108657265 | AGAACAGAGAGAAAG[C/T]TCAAGTGAAAGCAAG | 23603 |
rs772506206 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666113 | GACCTCTAAGGATGA[A/G]CAAGACTTAGGTGAA | 23603 |
rs772559175 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709938 | TAATAAAGAGGAAGA[C/T]GATGTAGCAGTAAGT | 23603 |
rs772591629 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654862 | AGGCACATGCCACCA[A/C]CCGTGGCTAATTTTT | 23603 |
rs772593381 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703777 | AGGCCTGACTATGGG[-/C]CCTGGATGACACCCA | 23603 |
rs772609225 | in-del | -/G | 1.64969e-05 | 0.00287196 | frameshift-variant, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662122 | CCACAGGTTCAGTCA[-/G]GGAAAGGGTGAGTCC | 23603 |
rs772627304 | snp | C/T | 1.64895e-05 | 0.00287132 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654329 | ATAAGTAAATGATGC[C/T]GGTGTCAGGGTCATA | 23603 |
rs772648214 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718627 | TGTTTCTGGAATTTT[C/G]AGACATCCTATAGAA | 23603 |
rs772663301 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698905 | ACACACACTTTAATA[C/G]ACAAAAATCTCACAT | 23603 |
rs772670611 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707453 | ACTCTTCTCAACAGA[C/T]GGTACTGGGACAATA | 23603 |
rs772737528 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661351 | AAAATAGGAAGAGAG[C/T]TTAATGGCACGTGAA | 23603 |
rs772754388 | in-del | -/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701014 | CTTCAATTACATCAG[-/T]AGTCTAATGGTTTCA | 23603 |
rs772755108 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711183 | GCCCAGGCAACATAG[C/T]GAGACCCCATATCTA | 23603 |
rs772764522 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706336 | TAACTCAATATTCAA[C/T]GGCGAAAGATGCCTT | 23603 |
rs772825035 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645426 | CATCAACAACTTTAC[C/T]TCATTAATTCGATAT | 23603 |
rs772842663 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713823 | TCCACATCAGCCAAC[A/G]ATGGCACTTAGAGCT | 23603 |
rs772843096 | snp | A/G | 8.32688e-05 | 0.00645194 | intron-variant | CORO1C | GRCh38.p7 | 12:108657300 | AAGCCTGGGGAGGGC[A/G]TACCGGATTCCAGAG | 23603 |
rs772863022 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683919 | AATGTAACACCTTGA[C/T]ACAAAGGACAGTATA | 23603 |
rs772919938 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648668 | CTTCTTGTTTGCAGT[A/G]GGCTTGCTATCCAGA | 23603 |
rs772957986 | snp | C/T | 3.32585e-05 | 0.00407776 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647368 | AAGCACAAGTTCTTG[C/T]TCCCATTTTTTCTGT | 23603 |
rs772992826 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724956 | ACAGGATGTTACACT[G/T]TATCACACTGTAACC | 23603 |
rs773011352 | snp | C/G | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108657423 | GTGCTTTCTCCTTCT[C/G]CTGGAGAGCAAAAAG | 23603 |
rs773036091 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702402 | GGTTCCTAGGCTGTC[G/T]TATGTGTCATTTCAG | 23603 |
rs773091620 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645004 | CTTACCCCCGGAGAG[A/G]AGTATGGCACCGTGC | 23603 |
rs773099874 | snp | C/T | 3.30196e-05 | 0.00406309 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662077 | GCCAAGCCACGATGC[C/T]GACTCTCTTTGAGTG | 23603 |
rs773128963 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681938 | CAATACCATTTAAGG[C/T]AAAAGGCATATGATC | 23603 |
rs773150683 | snp | C/T | 6.59152e-05 | 0.00574049 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652385 | GTACGGGGATTCATC[C/T]GTGATCTCAAAATAG | 23603 |
rs773191150 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726990 | GAGTTACCCCATTCA[C/T]GTTATTTTAACATAG | 23603 |
rs773220496 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667773 | GTAAAATCCCATTGT[A/G]GTTCTGGAAAAAAAC | 23603 |
rs773291312 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720469 | ATATAAACATCTTGC[C/T]AACATATTTATTTAC | 23603 |
rs773295626 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714507 | AGACATTACAGGTGC[A/G]GTGGTTCACACCTGT | 23603 |
rs773308727 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721844 | GCCCTGATCAACTTT[C/T]CAAAGGTCACAGAAA | 23603 |
rs773344481 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689384 | ACATTCATTCGAGTG[A/G]TAAGTCAAATCAAAT | 23603 |
rs773386133 | snp | A/G | 1.65397e-05 | 0.00287569 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678296 | GCAGTCCTCTGAACC[A/G]CTGGCAATGACCTGA | 23603 |
rs773405435 | snp | G/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703347 | GAAGAATTTACAAAA[G/T]AAACACAAACAGCAC | 23603 |
rs773571948 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714667 | CTCAGGAGGCTGAGG[A/G]CAGGAGGATTGCTTG | 23603 |
rs773603080 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646929 | AAAAAAAACCACACA[C/T]ACAAATACTGCAAAG | 23603 |
rs773677935 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697936 | AAATTATAAGGTAGA[C/T]ATCAAGAAGGCAGTC | 23603 |
rs773690901 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704554 | TGATATAGAAGTTCT[C/T]TTGCTACAATCACAG | 23603 |
rs773707990 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108730084 | GACCAGTTTATTAAA[A/C]GCGCACTACATTCAA | 23603 |
rs773718275 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664881 | TCAAAGCATGAAGTC[C/G]ACAGAAAAACAATTA | 23603 |
rs773732877 | snp | A/G | 1.72015e-05 | 0.00293265 | intron-variant | CORO1C | GRCh38.p7 | 12:108678406 | CAGTCTGAAAGAAGA[A/G]AGAAACAAACCTATT | 23603 |
rs773765818 | in-del | -/AAAA | | | utr-variant-3-prime, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645117 | ACACCATTTTGTAAT[-/AAAA]CAATGATTTTTATCT | 23603 |
rs773770084 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710129 | ATACAACAGCAACTA[G/T]TCTAGAATGGTTTTT | 23603 |
rs773781816 | snp | C/T | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108659087 | GGCCCTACCAGAGGC[C/T]CTACTTACTAACAGC | 23603 |
rs773877206 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673617 | TGGCTAGAGAGGAGA[A/C]GTCAATGCCTGGCTT | 23603 |
rs773896503 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715795 | GGTCTCACACCAACC[A/G]CAAAACTTTTATAGA | 23603 |
rs773909841 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658789 | CACTTTCTTGTCTTT[A/G]GAAGCTGTGCAGATC | 23603 |
rs773964681 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724756 | GAAAAAATATAACTG[A/C]CTTCCACATACAATG | 23603 |
rs773970345 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727731 | ACTAGTAAGACCCCA[C/T]TATTCATAAATTGGA | 23603 |
rs774129382 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664364 | CTGGATGAGTGTTTA[-/G]GGGTTCAGCTCAGTT | 23603 |
rs774161804 | snp | A/G | 8.37472e-05 | 0.00647044 | intron-variant | CORO1C | GRCh38.p7 | 12:108647527 | GCTTCATTTTGCTAA[A/G]AAAACAAAAAAAGGA | 23603 |
rs774193093 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712410 | GAAACTCCATCTCTA[C/G]TAAAATACAAAAAAT | 23603 |
rs774248993 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653481 | TACCACCCAGTGAAG[A/G]GCTATCTAACAGGTC | 23603 |
rs774260522 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666523 | GGCCTGTCATTATGT[C/G]GCTCTCTGCCCTCTT | 23603 |
rs774262858 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680637 | CAGTTTATTCCTTAA[A/G]AGCTGATGTGAGGAC | 23603 |
rs774294282 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655625 | GACCACGAGTAATCC[A/G]CCAGCCTCGGCCTCC | 23603 |
rs774331944 | snp | A/G | 1.64988e-05 | 0.00287213 | intron-variant | CORO1C | GRCh38.p7 | 12:108648880 | TGGCACCCGTGGGTA[A/G]GGAAGAAGAAAGGCC | 23603 |
rs774332255 | in-del | -/TC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682938 | AAAATCATAATGGAT[-/TC]AACAGAATGAAAGTT | 23603 |
rs774379995 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702178 | AAAGCCAGGTACTGG[C/G]CTAGGAAGCTATTTG | 23603 |
rs774400829 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695634 | GATAATGAACAGGAA[C/G]AAAAGACCACCAAGT | 23603 |
rs774455620 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654317 | TTACCTTTCCACATA[A/G]GTAAATGATGCTGGT | 23603 |
rs774457412 | snp | G/T | 3.32436e-05 | 0.00407685 | intron-variant | CORO1C | GRCh38.p7 | 12:108662004 | AGTGGAAGACAAGGG[G/T]AGGACCGCTGAGCTC | 23603 |
rs774527125 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722637 | TCAACACAATAGATA[-/G]AAATTACTACTAGTA | 23603 |
rs774545567 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713615 | CTAGGCCTGGAGAGA[A/G]TTCCAAAGCTCATCA | 23603 |
rs774577738 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689246 | TAATCACTGGTTCCT[A/G]CAAGAAAGGAAATGT | 23603 |
rs774631156 | snp | C/T | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701148 | AGGGAGGACAAGGAA[C/T]GCTCCTCCCCCACTT | 23603 |
rs774640008 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651670 | GCCTCAGCTTGAAGA[C/T]TAAAGATGCATGTTT | 23603 |
rs774691563 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726654 | TCTCTACAAAACATT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 23603 |
rs774812533 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721661 | TTCTTTGAAACCAGT[A/G]GTTCAAACCCTTCAC | 23603 |
rs774812676 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708901 | GGGACCACAAGCGTA[C/T]GCCACCACACCAGGC | 23603 |
rs774816139 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714818 | ATCATACTTTTTAAA[C/G]TTTTCAAAGAAGAGC | 23603 |
rs774838589 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685582 | TACTAGATTTGGATA[C/G]GGAAAGAAAATTTCC | 23603 |
rs774845604 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108723767 | GTCTGTTACAATCTA[C/T]ATATTAATAGTTCAG | 23603 |
rs774862106 | snp | A/G | 3.314e-05 | 0.00407049 | intron-variant | CORO1C | GRCh38.p7 | 12:108652427 | GTCACCCTGTAAGAA[A/G]CCAGAGACAAGTCTG | 23603 |
rs774883777 | in-del | -/CTGAGGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715670 | ACTCACAACACTGGC[-/CTGAGGA]AGCAGCCATCTCCCT | 23603 |
rs774899798 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728623 | GAAGCTGTTATAAAA[A/C]AAAAAAAGTTCCATT | 23603 |
rs774900565 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720106 | TGGGAGGATCACTTG[A/G]GCCTGGGAGGGCGAC | 23603 |
rs774905941 | snp | A/G | 1.69312e-05 | 0.00290952 | intron-variant | CORO1C | GRCh38.p7 | 12:108647544 | AAACAAAAAAAGGAG[A/G]CAGTGATTAAAATGC | 23603 |
rs774908620 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646777 | ACAGTCATCAAAATG[A/T]CCAGGTTTGTGCTGC | 23603 |
rs774914708 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650762 | GACATTCTGAACAAC[C/T]GTGTTTATAGTCTGT | 23603 |
rs774927612 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729973 | AGAGCCCTACAAGTA[A/C]TGTTTTAGAATGTAA | 23603 |
rs774928614 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697690 | ATCATATTTCTTCTT[C/T]GAGGCTGTACTTCTA | 23603 |
rs774934034 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696192 | GGGTGAAATCAGCTA[C/T]CATTCCAATTCACCA | 23603 |
rs774940353 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716280 | GTTTTTCACTACTTA[A/G]TCATATGGAGTAGAC | 23603 |
rs774951780 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670289 | TGAGGGCAGCAGGCC[A/G]GTGTGAGATCAGCAG | 23603 |
rs774972592 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685015 | CTGAGCTCTGAACTT[-/C]CAAGAACACCAAATG | 23603 |
rs775054781 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648641 | TTTCTTGGGGATGCT[A/G]ATCAGGTCGCACTTC | 23603 |
rs775132188 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684200 | GTGAAAAGATACTTC[A/T]ATCTCACTGATAATT | 23603 |
rs775201477 | snp | A/C/T | 6.67093e-05 | 0.00577502 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658690 | AGCAGAAAGCTCACA[A/C/T]TCACTCAAGTGCTCC | 23603 |
rs775216176 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715506 | CTCCACATCTCCCAA[C/T]TTTCTGCTTATCACC | 23603 |
rs775229652 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724870 | AGGAACTGTATTTTT[C/G]TTATTAATGTAAGAT | 23603 |
rs775238496 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701159 | GGAACGCTCCTCCCC[C/G]ACTTGCCTCTATGAT | 23603 |
rs775279256 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108647723 | TCTATCTGAGATCCC[A/G]TGGCAAAACAACAGT | 23603 |
rs775308944 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694282 | AGCAAGACTGTCTCA[-/AAAAAAAAAAAAA]AAAAAAAAAAAGCAA | 23603 |
rs775395550 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691847 | CCAGGGGAGGGGGTG[A/G]GGTGGAAACCATCAT | 23603 |
rs775429948 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720812 | ACAGGCATGAGCCAC[C/T]GCACCCGGCAAATAT | 23603 |
rs775468842 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693498 | TATTCTAGTTCTTTT[-/C]CCCATAACAATCAAG | 23603 |
rs775481052 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651544 | AGGACCAGTGGGGCC[C/T]CAAATACAGTTTTGA | 23603 |
rs775501569 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680500 | GCAGCGAAGTATAAA[C/T]GGTTGAGAACCAGAC | 23603 |
rs775589452 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700959 | TAATGATTCTCTGTT[A/T]GAGAAAAACTGATGT | 23603 |
rs775589468 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108693089 | AAGCTTGAGCCACCG[C/T]GCCCGGCTAAACCAC | 23603 |
rs775597406 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648800 | TTCTGCCTCCAGCGC[G/T]GCCTCTGGCCCCGCT | 23603 |
rs775598603 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724454 | AAGCTCCTGCCACCA[A/C]AGTCTCCTCATCTGT | 23603 |
rs775716103 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108654330 | TAAGTAAATGATGCT[A/G]GTGTCAGGGTCATAG | 23603 |
rs775764847 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701311 | CTCTGTCGTACCACT[C/T]GCCTCATCGTGTCTG | 23603 |
rs775785451 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688427 | GTATTACACATGTAC[C/T]GCAGCCATGTTCACC | 23603 |
rs775787099 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712572 | AGCGAAACTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs775841137 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732093 | TCCTAGCATCTCAAG[C/T]CCCGCCCACTACCCC | 23603 |
rs775872605 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702769 | TAAATGCAGAGAGAC[-/G]AATTTATTTTTGCCA | 23603 |
rs775873778 | in-del | -/TGTC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664310 | AAGGAGACAAACAAT[-/TGTC]TGTTTTCAATTGCTT | 23603 |
rs775876856 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718681 | TCTTACTGCACCTTA[A/G]GAAAAATAATTTTGT | 23603 |
rs775879891 | snp | A/C | 1.67837e-05 | 0.00289682 | intron-variant | CORO1C | GRCh38.p7 | 12:108678265 | ACACAACACCCTGGG[A/C]GCTTACCATGACCGT | 23603 |
rs775897016 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702080 | AAAAGTATTTAAATG[G/T]AAAGCAATGTGATCA | 23603 |
rs775954211 | in-del | -/AAAC | 1.7221e-05 | 0.00293432 | intron-variant | CORO1C | GRCh38.p7 | 12:108678409 | TCTGAAAGAAGAGAG[-/AAAC]AAACCTATTATGTAA | 23603 |
rs776155391 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | CORO1C, LOC105369968 | GRCh38.p7 | 12:108645706 | CATTACTCCAAGTTC[A/G]GCTGTCACCACACTC | 23603 |
rs776162190 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674315 | CACCTTTGGGAGGCC[A/G]AGGCGGGCGGATCGC | 23603 |
rs776176931 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694369 | ATGTGAATGAATGAA[C/T]GTGATTTTTCTAAAG | 23603 |
rs776200455 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685569 | CACTGACCAACCATA[C/T]TAGATTTGGATAGGG | 23603 |
rs776233852 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646597 | ATAATCATCTGAAGC[A/G]CAGGATAACCGAGAA | 23603 |
rs776247979 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108655244 | TTTTCCCAAGCATGA[C/T]TATTTTGATTTAGAC | 23603 |
rs776269561 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668963 | AAAAGAACTCACAGA[A/G]CCAAAACTCTGCAAA | 23603 |
rs776403648 | snp | A/G | 4.99604e-05 | 0.00499777 | intron-variant | CORO1C | GRCh38.p7 | 12:108661990 | CAGAGAGCCACAAGA[A/G]TGGAAGACAAGGGGA | 23603 |
rs776422622 | in-del | -/CAAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683754 | TCACCACCTCCCAAT[-/CAAT]CAATCAATCAATCAG | 23603 |
rs776429432 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663034 | AAATAGACATTTCAA[A/G]GAAGACATATAAATG | 23603 |
rs776455083 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658841 | CTCACATTGTAAATC[A/G]TGTCTGAATGCATAT | 23603 |
rs776527538 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703623 | CCAAGGAGAAACTGT[A/G]TGTCTCCAAAGACAG | 23603 |
rs776558672 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648658 | TCAGGTCGCACTTCT[G/T]GTTTGCAGTGGGCTT | 23603 |
rs776573433 | snp | A/G | 1.71073e-05 | 0.00292461 | intron-variant | CORO1C | GRCh38.p7 | 12:108678397 | CAATTCGACCAGTCT[A/G]AAAGAAGAGAGAAAC | 23603 |
rs776620587 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716809 | CATTACTTACTAACA[A/T]CCACAGGGTTATACG | 23603 |
rs776658865 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108665179 | AGCAGAGCTCATAAT[A/G]GGGACTTAACCTTTT | 23603 |
rs776725679 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108710286 | CCCTCACCAAGTTTT[C/G]CAGGTGATACTGAAG | 23603 |
rs776750481 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666315 | ACAAGGACTGCAATG[C/T]GAGAAGAAAGTGAGT | 23603 |
rs776838445 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691771 | TGCTGTGGACATATC[A/C]GTGAACTGCAGCAGC | 23603 |
rs776850111 | snp | A/G | 1.65048e-05 | 0.00287265 | intron-variant | CORO1C | GRCh38.p7 | 12:108648892 | GTAAGGAAGAAGAAA[A/G]GCCTGGGATTTTTGA | 23603 |
rs776896693 | snp | C/G | 1.67618e-05 | 0.00289493 | intron-variant | CORO1C | GRCh38.p7 | 12:108657289 | AAGCAAGTGGAAAGC[C/G]TGGGGAGGGCGTACC | 23603 |
rs776921387 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108699234 | AAAACCAAATCATAA[G/T]ATCAGTTAGCTGGGG | 23603 |
rs777006236 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731872 | CTGCAAGGCCACGTC[C/T]CCTGGCTCCTCAAAG | 23603 |
rs777107755 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687026 | CCGTCCCAGATACAA[A/G]CACTATCATTTGCTT | 23603 |
rs777110097 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672424 | ACGATTTTCAGTATC[A/G]TGGTATGGTGGTGGT | 23603 |
rs777198441 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717203 | CAGCTGGGAGGAACA[A/G]CAAAATATCAAAAGT | 23603 |
rs777200000 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674264 | GGATCTGGGCAAAGT[A/G]AATTAAAAACCTTCT | 23603 |
rs777258244 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108676769 | AAAGTGAGACTCCAT[C/T]CCAAAAAAAAAAAAA | 23603 |
rs777298579 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719541 | AATTCTCAAGTCAAA[C/T]GAATTCTCAAATACA | 23603 |
rs777303885 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688236 | TATTTATCGATCTCA[C/T]ATCTCCTTCTAAAAA | 23603 |
rs777305764 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721283 | CATAATCAGGGCCAT[C/G]TCATCTACCCATCTT | 23603 |
rs777515716 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686356 | AAGGAAGATGTACAA[G/T]AATTAAAGCCAGCTT | 23603 |
rs777526999 | snp | A/G | 1.64784e-05 | 0.00287035 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658760 | ATCTCTTGTTTCCTG[A/G]GATCAATGACTCTCA | 23603 |
rs777569084 | snp | A/G | 0.000115606 | 0.00760195 | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647397 | GTAGGGGTGGGGGTG[A/G]GACCTTCAGGCTGCT | 23603 |
rs777580144 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675414 | AAAAGGCGAGAAAGT[C/T]GGCTTTGAGATAAGA | 23603 |
rs777587143 | snp | A/C | 1.6495e-05 | 0.0028718 | intron-variant | CORO1C | GRCh38.p7 | 12:108648872 | GAGACATTTGGCACC[A/C]GTGGGTAAGGAAGAA | 23603 |
rs777613119 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709434 | TCTCCCATTTCAGCA[C/T]GGTATTTCTGCAGTT | 23603 |
rs777670099 | in-del | -/GAATACTT | 1.6808e-05 | 0.00289892 | intron-variant | CORO1C | GRCh38.p7 | 12:108652245 | AGTTACACCAACCTA[-/GAATACTT]GACAATCTCGATTCT | 23603 |
rs777671951 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728291 | TCATCAACTGATGAA[C/T]GGATAAACAAAATAC | 23603 |
rs777679248 | in-del | -/AGAC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721768 | AAAGAATAGAAAAAT[-/AGAC]AGGACGAGTGCCCAG | 23603 |
rs777697259 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716336 | AATACTGTTATACCA[-/G]GAAATGAAATTACTG | 23603 |
rs777800236 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692960 | GTGCCACCATGCCCA[C/G]CTAATTTTTGTATTT | 23603 |
rs777816975 | in-del | -/GAGA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652071 | TTTTTTTTTTTTTTT[-/GAGA]GAGATTTTTTTCTAA | 23603 |
rs777817834 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701256 | GTCATCATAGCACTG[A/G]TCATTTTTCACCGCT | 23603 |
rs777883416 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691738 | ACTGTCAGAGCCCTG[C/T]CAGGCCTGCGGGCCG | 23603 |
rs777949815 | snp | A/C | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108657658 | TTAACTCAGAAGACT[A/C]GCTCTCTCCACCATA | 23603 |
rs777950844 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679130 | AAAAAAAAAAAAAAA[-/G]AAACAAGAAAAAAGA | 23603 |
rs777970696 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716742 | ATCCTTCTTTCACTG[G/T]GATACAGTCCACATC | 23603 |
rs777989188 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692617 | AAATGTGAACTGCTG[A/C]GATTTCATCACTGTC | 23603 |
rs778043997 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649416 | GTATCTACAACGCGG[A/G]TACAAGGTCTTCTGC | 23603 |
rs778060850 | snp | A/G | 3.30017e-05 | 0.00406199 | intron-variant | CORO1C | GRCh38.p7 | 12:108654288 | GATTTAACACCAAAC[A/G]TCAAAATTACTGTTT | 23603 |
rs778100587 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680118 | AGTGCTGGAGATACA[A/G]ACGTGAACAAGGCAG | 23603 |
rs778128495 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687692 | CAGGAGGCTGAGGCA[C/T]GAGAATCGCTTGAAC | 23603 |
rs778158159 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108667023 | CATGGCTTACTGTGC[A/G]GATACAATAACTAAA | 23603 |
rs778158271 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712199 | TTCAATAGAAAAAGG[A/C]AGGTAAGACAGCAGA | 23603 |
rs778228023 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108719162 | TATGCTAAATTAATT[A/G]GACATCACAATAGTA | 23603 |
rs778248198 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108727800 | CACCATCAAGAAAAT[-/G]AAAGGACATGTCAGA | 23603 |
rs778257229 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722665 | GTAGATCTGAGTTCC[A/C]AATAACTGAGTTAGA | 23603 |
rs778259532 | snp | A/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647482 | GTGTCTTTTATAGAT[A/T]TGATCTCTTTTAAAA | 23603 |
rs778270031 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, upstream-variant-2KB, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108658886 | AGGGCTTCCCCTGTT[C/T]CCACATTCCAGATGA | 23603 |
rs778342311 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675189 | TTAAATGTATATATA[C/T]ATATACATAATGCTA | 23603 |
rs778356180 | snp | A/G | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108733249 | AGTCCACGGCTCACT[A/G]CAGCATGGACCTCCC | 23603 |
rs778420492 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690883 | GCATTCAATATCAAA[A/T]CAGAAAATAGAGAAA | 23603 |
rs778431340 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648609 | CTGGTCCTCACCACA[C/G]TGGCCGTGTCTGTGG | 23603 |
rs778442314 | in-del | -/AA | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660454 | GAAACTCCATCTCAA[-/AA]AAAAAAAAAAAAAAA | 23603 |
rs778446633 | snp | A/C | 1.65381e-05 | 0.00287555 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658925 | TTATCACAGCCTAAA[A/C]CAGGCAAAACCATCA | 23603 |
rs778454300 | in-del | -/AAAGG | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661238 | TCTCCAATTTTAGAT[-/AAAGG]AAAAGATTTCTGTAC | 23603 |
rs778467707 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687882 | AATCTTACTGGAAAA[G/T]CACAACAGCTTCCAC | 23603 |
rs778547796 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701530 | GGAAAGAATTACAAA[G/T]AAATGAAAAATTCCT | 23603 |
rs778553708 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713103 | AAAAACATGCCTTAC[C/T]TATTTTAATAGAAGC | 23603 |
rs778590556 | snp | A/G | 3.30579e-05 | 0.00406544 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662051 | AAGAAGCACATTGCG[A/G]GCCGTTGGATGCCAA | 23603 |
rs778630045 | snp | A/T | | | downstream-variant-500B, nc-transcript-variant | CORO1C, LOC105369968 | GRCh38.p7 | 12:108644862 | CCCATCCCAGGACAC[A/T]CCGCTGGCAAAGGTC | 23603 |
rs778635679 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700340 | CTTTTTTTTCTTCAT[C/T]ATTTGCAGTTCTGGG | 23603 |
rs778716501 | snp | A/G | | | | | GRCh38.p7 | 12:108660920 | TTTATTTAACTCACT[A/G]TGAGTCATAAACATT | 23603 |
rs778742004 | snp | A/G | | | | | GRCh38.p7 | 12:108688795 | AATCCCAGCACTTTG[A/G]GAAACCAAGGCAGGC | 23603 |
rs778745729 | snp | A/C | | | | | GRCh38.p7 | 12:108708415 | TATATGAAAGTCCAG[A/C]ATAGGCAAATCTAGA | 23603 |
rs778746727 | snp | A/T | | | | | GRCh38.p7 | 12:108719441 | AGACTTTAGTATGTA[A/T]AAATGAACTCCTAAG | 23603 |
rs778826707 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714271 | GCGCACAACTGTAGT[C/T]CCAGCTACTCGGGAG | 23603 |
rs778834106 | snp | A/T | 1.64773e-05 | 0.00287026 | intron-variant | CORO1C | GRCh38.p7 | 12:108701104 | GGGTGTCTACCAGAA[A/T]GGAAGATCAAATTAC | 23603 |
rs778840269 | snp | A/G | 3.3071e-05 | 0.00406625 | intron-variant | CORO1C | GRCh38.p7 | 12:108649026 | TTTGAAGAATCTTCA[A/G]AGGGGAAATAAAGGC | 23603 |
rs778845008 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709269 | ACTGTCTAACAAATG[C/T]TGGCAATTATTATTT | 23603 |
rs778889131 | snp | A/G | 1.67854e-05 | 0.00289697 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108678373 | CACATACTGTAGGGT[A/G]AGATTTGTCAATTCG | 23603 |
rs778937920 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695500 | TCCGTTAAGTGAATA[A/C]TAATTTTAATAATGT | 23603 |
rs778941906 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715988 | ATGCAAAAATTGGCC[A/T]GGCGTGGTGGCACGC | 23603 |
rs779002250 | snp | C/T | 0.000334784 | 0.0129337 | synonymous-codon, intron-variant | CORO1C | GRCh38.p7 | 12:108702848 | GCTGGGGGCATGTAG[C/T]CGGGCTGAAGTAAGA | 23603 |
rs779004231 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108728725 | CTAGGGCAAAGAAAA[C/T]CCAGAGAGATTCTAT | 23603 |
rs779021476 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729103 | CTCGTCGACATACCC[A/G]CTTATATAACTAAGA | 23603 |
rs779095395 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108654845 | GAGCTGGGATTATAG[A/G]TAGGCACATGCCACC | 23603 |
rs779126535 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108684685 | TATTCTACCTGTATC[G/T]GTTATGCTTTATTAC | 23603 |
rs779179662 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670966 | ACACAACAAATAATG[C/T]CCCCAAAAGAAATAA | 23603 |
rs779199219 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664064 | TACAGGTAAGCTGAG[C/T]AGCATCAAGAACCCT | 23603 |
rs779218648 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108715098 | ACTGGGCTGGGTGTG[G/T]TGGTTCATACCAGTA | 23603 |
rs779233638 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108691450 | TCTTTACCGGAGATA[C/T]AGCAGCTTTCCCAGA | 23603 |
rs779291703 | in-del | -/ATAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685226 | TATTCTTCAGTCAAG[-/ATAT]CTGAGAATAATAATA | 23603 |
rs779324217 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108678983 | GGTCGTGGTGGTGTG[C/T]GCCTGTAGTCCCAGC | 23603 |
rs779338905 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650717 | GTCCTGGCATACAAT[A/C]AATGCTCAAGAAACA | 23603 |
rs779418934 | snp | C/T | 6.58957e-05 | 0.00573964 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108701268 | CTGGTCATTTTTCAC[C/T]GCTTGCCCAAATACA | 23603 |
rs779422183 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679892 | ACTCCCACAATTACC[A/G]TAAGGATTAAATGAG | 23603 |
rs779433483 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692274 | GAATGGGCATCCCAC[A/G]ACATGTCAGGACACT | 23603 |
rs779512526 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687702 | AGGCACGAGAATCGC[G/T]TGAACCTGGGAGGCA | 23603 |
rs779523160 | snp | C/T | 4.95667e-05 | 0.00497804 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108662056 | GCACATTGCGGGCCG[C/T]TGGATGCCAAGCCAC | 23603 |
rs779554696 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108657494 | GGAGAAACTCGGGCA[C/T]AGATCCAACCTCACC | 23603 |
rs779575841 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648754 | TCAAGGAGATGAGGA[C/T]TGGGTCTGCATTCTT | 23603 |
rs779582898 | snp | A/G | 1.65971e-05 | 0.00288067 | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658937 | AAAACAGGCAAAACC[A/G]TCAGAGATTAGAAGA | 23603 |
rs779586627 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108687966 | ACTCTGTCACCCAGG[C/G]TGGAGTGCAGTGGTG | 23603 |
rs779593873 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108698786 | AAGAGACACATCCAC[A/G]TCCCACTACAAGTCA | 23603 |
rs779683270 | snp | A/G | 4.96438e-05 | 0.00498191 | intron-variant | CORO1C | GRCh38.p7 | 12:108662164 | TCTGCCATACCTGTT[A/G]GACAAGGAAGAAAGA | 23603 |
rs779704617 | snp | C/T | 8.23649e-05 | 0.00641683 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108648815 | GGCCTCTGGCCCCGC[C/T]GTGTCAGGATACAGG | 23603 |
rs779747241 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108650477 | AACCACCACTCCTGG[A/C]CCAAAAACATTTTTA | 23603 |
rs779748708 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652479 | ATCTGGATTATGGGG[A/G]TGTCTCTCTCCTCTA | 23603 |
rs779757973 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666059 | ATTAGCTTCCTGCTA[A/G]CCAAGCTTGGTCCAC | 23603 |
rs779764528 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108685672 | GGCCATCAGAAACAC[-/A]GTTAATAAAAAATGA | 23603 |
rs779773855 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711103 | CACAGTGGTTCATAG[C/T]TGTACTCCCAGCATT | 23603 |
rs779775779 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724050 | TATCCAAGAGATATC[A/C]TGTATTTTCAAGTTT | 23603 |
rs779776182 | in-del | -/AAAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673896 | AATAAAATAAAAAAT[-/AAAT]AAATAAATAAATAAT | 23603 |
rs779779497 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674762 | TTGCTGCAATCTCAT[A/G]ATAAAACTTGAACAG | 23603 |
rs779779597 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108659652 | ACTAAAAGTAAAAGG[A/T]TTAAATGACTGTTTA | 23603 |
rs779788912 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108708090 | CTCAAACAATTAAAC[A/G]AAGCATTATCATAAG | 23603 |
rs779864485 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108717815 | TTTATTTTTTAAAAC[A/G]TAATTACCTTTCCAC | 23603 |
rs779885523 | snp | A/C | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108732879 | TGGCATTACTTTTTG[A/C]CATTAAAAGGAATGG | 23603 |
rs779966443 | in-del | -/AT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108700512 | GAAGTTGAAGAAAAC[-/AT]AGAACCATTCTCAGT | 23603 |
rs779970049 | snp | A/C | 8.25457e-05 | 0.00642386 | intron-variant | CORO1C | GRCh38.p7 | 12:108654270 | AAATGTTTCCACTTA[A/C]AGGATTTAACACCAA | 23603 |
rs779973832 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673330 | AGAGCAAAGTCCTAA[C/T]TCTCTTCAATTCCAT | 23603 |
rs780009474 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108672899 | AACTTCATCGATAAA[C/T]GCTGTGTGTTTTCTC | 23603 |
rs780026837 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108664947 | TTTTGCAAGATGCAC[A/T]GTGACCCCACTTAGA | 23603 |
rs780053892 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689132 | TTGAACCCGGAAGGC[C/G]GAGGTTGCAGTGAGC | 23603 |
rs780060244 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706804 | GGTCAGACTGGTCTC[A/G]AACTCTTGACCGCAG | 23603 |
rs780122698 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108646040 | GAGAGGCAGGGCAGG[A/T]TAGTTGTGCGGAGGG | 23603 |
rs780233097 | snp | C/G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668300 | CCGAGTGTTGGGTTC[C/G/T]GATCTGCCAGGGTTA | 23603 |
rs780247653 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108653500 | ATCTAACAGGTCTAG[C/G]GACTACCTCAACAGC | 23603 |
rs780264614 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694943 | ATTAGTTATCAACTG[C/T]TGATTAACAAGTTAT | 23603 |
rs780272341 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713458 | GGTAACAGGTAAGAT[A/G]CCAAGAATGAGGCAT | 23603 |
rs780286681 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726128 | GTGAGCCACCACGCC[C/T]GGCATGAAATATTTT | 23603 |
rs780316652 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108649425 | ACGCGGGTACAAGGT[C/T]TTCTGCCAGCTTGAG | 23603 |
rs780319369 | snp | C/G | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647419 | CAGGCTGCTATCTTT[C/G]CCATCTGCTGTTCTA | 23603 |
rs780348232 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666326 | AATGCGAGAAGAAAG[C/T]GAGTGAAAAAGTCTC | 23603 |
rs780357645 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108695572 | AAGAGAACCCAATGG[A/G]TGAGTTCCTCTGTTT | 23603 |
rs780455263 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690627 | CTTGCCCAAATATGC[A/G]ATAGCAACCAGAGTA | 23603 |
rs780544609 | in-del | -/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670256 | GGGAAGGGACAGCAA[-/G]GGGACACCTGACAGA | 23603 |
rs780606320 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108707624 | AGCAACAAAAGAAAA[A/G]TTAGAAAAACTGGAT | 23603 |
rs780658724 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | CORO1C | GRCh38.p7 | 12:108648858 | AGGTCAGACTACAAG[A/G]GACATTTGGCACCCG | 23603 |
rs780716263 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108711401 | AAGAAAGAAAAGGGC[C/G]GGGCATGGTGGCTCA | 23603 |
rs780723972 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108709749 | AGAGTAAATGAAAAA[A/G]TCCTGAACTAACACA | 23603 |
rs780802218 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108663922 | AATTGGGGACATGCC[C/T]GGGCACAGGGGGAGA | 23603 |
rs780814495 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722360 | AGCTTCAAATTAAGA[C/G]AGAGATGAAGGAGGA | 23603 |
rs780815867 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108721470 | ACCATCAAAGAGTCA[C/T]GTGCTTGAGGGCTGG | 23603 |
rs780839547 | in-del | -/ACTTGATAAAAGTAATTCAGTCC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108722833 | TATGTTATTTGTTCT[-/ACTTGATAAAAGTAATTCAGTCC]ACTGCACTCAAGACA | 23603 |
rs780847033 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108697460 | ATCTAAACATCATTT[C/G]TTGCTATCTTGATTT | 23603 |
rs780889572 | snp | C/T | 1.65067e-05 | 0.00287282 | intron-variant | CORO1C | GRCh38.p7 | 12:108648944 | AAAATATGGATTGTC[C/T]AGAAAACTCAGCACT | 23603 |
rs780890146 | snp | A/C | | | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647499 | GATCTCTTTTAAAAT[A/C]TCATCCAACTTGGCT | 23603 |
rs780892341 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108666020 | CAATGCTATGCTGGC[A/G]TAAGCCGACCGCACT | 23603 |
rs780895165 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729659 | TTACTATTATGCTTC[A/G]TAGCCAAACATTATG | 23603 |
rs780951109 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108686526 | TCTAGAATATTACTA[C/G]TTTTCTGGCATGAAA | 23603 |
rs781001031 | in-del | -/AGTT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108696620 | CAAGGCAGCTTGTGC[-/AGTT]AGTTGTGGCAAGAAA | 23603 |
rs781001674 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108671693 | ACTTTGACAGCAACA[C/T]CTATGCCAAAAGAAA | 23603 |
rs781016351 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673145 | GGCCAAAAGCTAAGC[G/T]CCTCTTAAGCCAGTT | 23603 |
rs781091738 | snp | A/G | | | intron-variant, upstream-variant-2KB | CORO1C | GRCh38.p7 | 12:108658106 | CTTTTGTCAAGGTAT[A/G]TGATTTTGTTGAGGT | 23603 |
rs781294902 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108716914 | ACTCGGCTTTGACCA[C/T]GCGCCTAGCACCATG | 23603 |
rs781384281 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108713347 | TTGATGTTGGTTCAA[C/T]TGATTATAACACCAG | 23603 |
rs781387637 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680421 | CAAAAAAGGAAATTC[C/T]AATGAACACCATATC | 23603 |
rs781398440 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108724325 | CATGTCAGGTTCACA[C/T]TGTTAAATAAAAAAT | 23603 |
rs781404983 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108682835 | ATCTTCTGAGTATAA[G/T]GCAATACAATTAAAA | 23603 |
rs781418191 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681395 | GTGAAAACAAATTCT[G/T]ATCTATTCATATCCT | 23603 |
rs781488103 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668215 | CACAAAGGCCTGCAT[A/G]TAGGGCATCAGGGCA | 23603 |
rs781489989 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108651157 | ATATAAAAAAGGGGC[C/T]TATAAAAATTCTCTT | 23603 |
rs781501120 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108647461 | CGCTCATCTTGATTG[A/C]AGATTGTGTCTTTTA | 23603 |
rs781504185 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108720354 | CTGCTTTTTATCAGA[A/T]CATATGCTTTAAATA | 23603 |
rs781521935 | snp | C/G | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | CORO1C | GRCh38.p7 | 12:108652358 | GCTGCTGAATGTGTT[C/G]AGGTAGTGGACGTAC | 23603 |
rs781572602 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108701681 | TTCCCCTTTTACAGA[A/T]AAGAAAACTCCAAAG | 23603 |
rs781584526 | snp | A/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108704669 | AGCTTGAAGGGCAGT[A/G]TGAGCCCATTCACTT | 23603 |
rs781663913 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712357 | GACAGGTGGATTGCC[C/T]GAACTCAGGAATTCG | 23603 |
rs781678078 | snp | A/G | | | missense, intron-variant | CORO1C | GRCh38.p7 | 12:108702855 | GCATGTAGCCGGGCT[A/G]AAGTAAGAGACCCTT | 23603 |
rs781737744 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108688923 | TAATCCCGGCTACTC[A/G]GGAGGGCTGAGGCAG | 23603 |
rs796080722 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656097 | AGTGAGGAGCCCCTC[C/T]GCCCGGCAGCCGCCC | 23603 |
rs796092257 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108660579 | TCCCTATAGGCAAAC[-/A]AGGTAACTTCAGCCC | 23603 |
rs796097219 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108692798 | TTAGACCACAGCTTT[C/T]TTTTTTTTTTTTTTT | 23603 |
rs796102411 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108683381 | CTGAGATCGCACCAT[C/T]GCACTCCAGTCCGGG | 23603 |
rs796121763 | snp | C/G | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703894 | CCACCTGCCTTACCC[C/G]ACAAGAGATCAGACA | 23603 |
rs796132360 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108674543 | ACAGAGCGAGACTCC[A/G]TCTCAATTTAAAAAA | 23603 |
rs796231503 | in-del | -/AAC | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706194 | TCTGAATCAAAAAAA[-/AAC]AAAAAAAACAAAAAA | 23603 |
rs796261507 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673293 | ACCAGCCACAAGATT[C/T]CCTTAAGCCAAAGCC | 23603 |
rs796271185 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108689516 | CAGACTGCTTTCTAC[A/G]CGGTTTCCCTTATCT | 23603 |
rs796271652 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108656342 | GAGGGAGGTGGGGGG[G/T]CAGCCCCCACCCGGC | 23603 |
rs796283435 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108681718 | TAAATTCTTAGATTT[A/G]TCTCAAAGAATTGCT | 23603 |
rs796311912 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108680592 | CATCCCTCAACCTCG[A/G]TTCCTCATCTATAAA | 23603 |
rs796340283 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108726561 | CGCCTATAATCCTAG[-/C]CACTTTCGGAGGCTA | 23603 |
rs796340514 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108673907 | AAAATAAATAAATAA[A/T]TAATTATGCTAAATC | 23603 |
rs796381882 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652042 | AAAAAAAAAAGTGAG[A/T]TTTTTTTCTTTTCTT | 23603 |
rs796428398 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108718384 | GAAAAAAAAAAAAAA[-/A]TACAAAAATTAGTGG | 23603 |
rs796433176 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108694350 | CAGGCACTAAGGAAT[C/G]AATATGTGAATGAAT | 23603 |
rs796437263 | in-del | -/GTAT | | | intron-variant | CORO1C | GRCh38.p7 | 12:108729393 | ATGTTTCATCGGTAT[-/GTAT]CTATTAAAATTCATC | 23603 |
rs796445504 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670071 | GGCAGCATTTTTTGG[G/T]GGTTTTTCCGAAGTC | 23603 |
rs796468656 | snp | A/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108712928 | TAAAAAAAAAAAAAA[A/G]AAAAAATCATCATTT | 23603 |
rs796475936 | snp | A/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679134 | AAAAAAAAAAAGAAA[A/C]AAGAAAAAAGAAAAA | 23603 |
rs796478668 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675493 | ATGAAAGGAACGGGG[-/A]AAAAAAAAACCCTAA | 23603 |
rs796507107 | snp | A/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108670829 | TAGTGATTCAAAATA[A/T]GAAAACAATATATAA | 23603 |
rs796567464 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108679155 | AAAAGAAAAAAAAAA[-/A]GAAATTTAAAAAGTT | 23603 |
rs796598371 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108690966 | GAAACCCTCTGTGAA[C/T]GCTGAAGAGCTCCAG | 23603 |
rs796610373 | snp | G/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725888 | TCGCCCAGGCTGGAG[G/T]GTGATGGCGCAGTCT | 23603 |
rs796624562 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108661805 | GCAGGAAATTCATAG[C/T]TTTCCTCAGGTTGTC | 23603 |
rs796670021 | snp | C/T | | | upstream-variant-2KB | CORO1C, LOC105369969 | GRCh38.p7 | 12:108731999 | CCGGCTCCCCTCCCA[C/T]TGCTTCAGAACTCGC | 23603 |
rs796674816 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675612 | TTCCTAAATGAACTA[C/T]ACTATTTGGTAACTA | 23603 |
rs796691173 | in-del | -/A | | | intron-variant | CORO1C | GRCh38.p7 | 12:108668517 | GCCTTCCCACCCGCC[-/A]AAAAAAAACTATATT | 23603 |
rs796726982 | snp | C/T | | | upstream-variant-2KB, intron-variant | CORO1C | GRCh38.p7 | 12:108703586 | AAGGACATCAAGGCC[C/T]ACTGTGAATCCCCAG | 23603 |
rs796745699 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675253 | ATAAACCAGGACTTC[C/T]GAAAGAAATGGCTTG | 23603 |
rs796746359 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108725110 | CCTGAATAGAGAAGA[C/T]TGTCTGAATAGACAT | 23603 |
rs796778508 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108705614 | GGGAACACTTTCAAA[C/T]TAATTGTATGAGGCC | 23603 |
rs796785935 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108669698 | AAAAAAAAGGCGGGG[C/G]GTGGCGGGGGGTGTT | 23603 |
rs796800705 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108714998 | TATGAAAATGACTGC[C/T]GAAAATCAAGTCTGA | 23603 |
rs796820764 | snp | C/G | | | intron-variant | CORO1C | GRCh38.p7 | 12:108675354 | CTCAAAGACTATGAT[C/G]GTCATTTCAAAAGGA | 23603 |
rs796867289 | in-del | -/C | | | intron-variant | CORO1C | GRCh38.p7 | 12:108706197 | AATCAAAAAAAAACA[-/C]AAAAAAACAAAAAAA | 23603 |
rs796898800 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108652198 | TTGAGATCTGAAGTA[C/T]ATGCTAGTCCAAGTA | 23603 |
rs796994301 | snp | C/T | | | intron-variant | CORO1C | GRCh38.p7 | 12:108702533 | AATTTTCCTATGTGC[C/T]ACTGCAGGACATTCT | 23603 |