SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs931543 | snp | A/G | 0.0951909 | 0.196316 | intron-variant, missense | CHD3 | GRCh38.p7 | 17:7889008 | ATCACAGTGTCTGCC[A/G]CCTTCATCACACAGG | 1107 |
rs1804966 | snp | A/G | 0 | 0 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912157 | ATGAGGGAGGAAGTC[A/G]ACTGCTGTTCAGCCT | 1107 |
rs2279620 | snp | C/G | 0.235953 | 0.249611 | intron-variant | CHD3 | GRCh38.p7 | 17:7889147 | TGGGGCCCTGACATC[C/G]TTTTGCCAAGAGGGA | 1107 |
rs3222385 | microsatellite | (CA)11/12/13/14/15/16 | 0.630362 | 0.147005 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884073 | TTNATGCCCCCCCAA[(CA)11/12/13/14/15/16]TTNAGTACACAGGGA | 1107 |
rs3744253 | snp | G/T | 0.0854556 | 0.188216 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883381 | ACGATCTTCAGATTT[G/T]ACTCTTTCCTCTTTA | 1107 |
rs4069875 | in-del | -/AC/ACAC/ACACACAC | 0 | 0 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884095 | CACACACACACACAC[-/AC/ACAC/ACACACAC]TTCAGTACACAAGGA | 1107 |
rs4239111 | snp | C/T | 0.203267 | 0.245593 | intron-variant | CHD3 | GRCh38.p7 | 17:7908680 | TTCCTTGATGGTTCC[C/T]TTTCCTTCATTGGTA | 1107 |
rs4321249 | snp | A/G | 0.316243 | 0.241064 | intron-variant | CHD3 | GRCh38.p7 | 17:7892211 | CACCATGGATCACCC[A/G]TGTCCGCACAAGAGT | 1107 |
rs5819184 | in-del | -/G | | | frameshift-variant | CHD3 | GRCh38.p7 | 17:7908822 | GTTCCTGGCCCGGAG[-/G]TTCAAGGTGGGAATG | 1107 |
rs5819185 | in-del | -/A | 0.372995 | 0.217652 | intron-variant | CHD3 | GRCh38.p7 | 17:7909553 | TGTCTGATAGCATTC[-/A]CATCCGTGCCCAATA | 1107 |
rs7222046 | snp | A/G | 0.3742 | 0.216966 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903211 | TCCTGAGGCAGCTCT[A/G]TGGGCAGCTTCTCCC | 1107 |
rs7224399 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CHD3 | GRCh38.p7 | 17:7900234 | GCTGATGCTGTGGGT[C/T]GGTCACTTGTCACTA | 1107 |
rs7342900 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906386 | GCAGGGGGACAGTTA[A/G]GACTTGGAGGGCTGG | 1107 |
rs7406836 | snp | C/G | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7891580 | AAATAGCAGAGATGG[C/G]CCAGGTGCAGTGGCT | 1107 |
rs7503751 | snp | A/G | 0.0410537 | 0.137264 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886224 | GACAAGTCACCCGGC[A/G]GCACTCTCTGGGCGG | 1107 |
rs8074053 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904920 | GGCGGTGAATGGAGA[A/T]GGTGTAGGATATGCG | 1107 |
rs9889381 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | CHD3 | GRCh38.p7 | 17:7889508 | CCAGAGTACTCGAAA[C/T]ACTTTCTGTTTGCAT | 1107 |
rs9889962 | snp | A/C | 0.461592 | 0.133149 | intron-variant | CHD3 | GRCh38.p7 | 17:7898191 | GAGGGTACAGTAGGG[A/C]CTGATTCAACCTGGA | 1107 |
rs9895704 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | CHD3 | GRCh38.p7 | 17:7897764 | ATCTCCAGGAATGTT[C/T]TGTGATAGCTGATTT | 1107 |
rs9896096 | snp | C/T | 0.0836992 | 0.186666 | intron-variant | CHD3 | GRCh38.p7 | 17:7889990 | CCTAGTGAAGAGCCT[C/T]GTTGTCAGTGTGTCC | 1107 |
rs9899375 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CHD3 | GRCh38.p7 | 17:7908297 | TCCTCTTCAGGAGCC[C/T]TTAGTTCCCTTTCAT | 1107 |
rs9909007 | snp | A/G | 0.0652144 | 0.168387 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906043 | GGAAGAGCTTTGGGT[A/G]TTCCTTTCTTCCTTG | 1107 |
rs11078713 | snp | A/G | 0.402277 | 0.198272 | intron-variant | CHD3 | GRCh38.p7 | 17:7892654 | GGTGCGCACCACTAC[A/G]CCCAGCTAATTTTTG | 1107 |
rs11554771 | snp | G/T | | | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912192 | AGGTAACTGAGCCAG[G/T]GAACGGCACCTTTAT | 1107 |
rs11650569 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886497 | GTGGCTTCTGTGGCA[A/G]ACGTTCCTGTCTAGC | 1107 |
rs11651304 | snp | A/C | 0.0899417 | 0.192045 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899136 | CACTGACACCATTCT[A/C]GCTGATGAGATGGGG | 1107 |
rs11651567 | snp | C/T | 0.101301 | 0.200969 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886457 | CCAACTCCGGGCTCT[C/T]TGTAAAACTGTCATA | 1107 |
rs11867454 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CHD3 | GRCh38.p7 | 17:7902473 | GTGTGACAAGAAGGT[A/G]GAATAATGAGGAGCT | 1107 |
rs12450454 | snp | C/G | 0.402982 | 0.197728 | intron-variant | CHD3 | GRCh38.p7 | 17:7890884 | AGACAGGCCTGTGTG[C/G]GGCCTGGAATAGGGG | 1107 |
rs12937681 | snp | C/G | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7901695 | tttgtatttttagta[C/G]agacgggatttcacc | 1107 |
rs12939868 | snp | A/C | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7901734 | caggatggtctccat[A/C]acctgacctcaggtg | 1107 |
rs12943165 | snp | G/T | 0.0475351 | 0.146656 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913224 | GTCTAGCTTACCAAA[G/T]ATTTGAACTGCTAGG | 1107 |
rs12945097 | snp | A/G | 0 | 0 | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912788 | TTTATGGGGGGGGGG[A/G]GTTTTTGGGGGGAGG | 1107 |
rs12950420 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CHD3 | GRCh38.p7 | 17:7910781 | GGCTCATAATGTCTC[C/T]CCTACAGCTTCTTTC | 1107 |
rs28391063 | snp | G/T | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7892181 | CCTTACTGCTGAACT[G/T]GGGGCTTTTCTCAGC | 1107 |
rs28391687 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | CHD3 | GRCh38.p7 | 17:7899650 | CCTTTCTCCTCTTCC[G/T]CCACCTGTCCTCCTG | 1107 |
rs28441558 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | CHD3 | GRCh38.p7 | 17:7899800 | CAGAGTAATGGCTCC[C/T]GTTGGGAGCCACAGT | 1107 |
rs28691002 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CHD3 | GRCh38.p7 | 17:7902035 | TGACACAATTTTGTA[C/T]GGATTTTCAGGGGGT | 1107 |
rs34009884 | in-del | -/G | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7890051 | AAGCTCTGGAAGACT[-/G]ATGAATTCAAGAGTC | 1107 |
rs34061762 | in-del | -/T | | | frameshift-variant | CHD3 | GRCh38.p7 | 17:7903919 | GCAACTGAGGACACT[-/T]GACGTGCAGAACATG | 1107 |
rs34196029 | in-del | -/T | 0.375 | 0.216506 | intron-variant | CHD3 | GRCh38.p7 | 17:7892497 | TTTTTTTTTTTTTTT[-/T]GAGATGGAATCTCAC | 1107 |
rs34320313 | in-del | -/G/GG | | | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886016 | GTGCGGTGGGGGGGG[-/G/GG]TCCCCCTCTTGACCC | 1107 |
rs34461368 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884477 | ATATATATATATATA[-/T]GTATATATATATATA | 1107 |
rs34543626 | in-del | -/A | | | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7911849 | GGCAGGGTCTTCCAA[-/A]GTACCTTCCTCCCAC | 1107 |
rs34551054 | in-del | -/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7897921 | CTTTCTGTTTGTGAT[-/G]CTGTGCAATATTTTC | 1107 |
rs34660030 | in-del | -/T | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7901527 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 1107 |
rs34823255 | in-del | -/A | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7908570 | GGCAAAAAAAAAAAA[-/A]GATGATTTCACACCC | 1107 |
rs34834032 | in-del | -/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890052 | AGCTCTGGAAGACTG[-/T]ATGAATTCAAGAGTC | 1107 |
rs34941534 | snp | A/C | 0.00179697 | 0.0299209 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7898529 | AGACCCTGCCCAGCC[A/C]CGCAAGTATAAGAAG | 1107 |
rs35240713 | in-del | -/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7901068 | TAGTGGGGAGGTGGG[-/G]TATTGAGCCACAGGG | 1107 |
rs35824822 | in-del | -/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7910186 | TTTCTCTCCATCTGT[-/G]CTTCTGTGGTAATCT | 1107 |
rs35860984 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7882937 | TCCACAGGCATGGAA[-/A]TGGGAAGCAAGGGAA | 1107 |
rs35997372 | in-del | -/C | | | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7911885 | AAGTATACACAACTT[-/C]CCCAGTAAATGGTTG | 1107 |
rs36123982 | snp | A/G | 0.0558544 | 0.157504 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885696 | TGGACAGGCAGAGTG[A/G]GGACGGTGTCCATCG | 1107 |
rs55752997 | snp | A/C | 0.177182 | 0.23916 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886730 | TGCCTCCGGCAGAGG[A/C]GCTGAAAAGAGGGAA | 1107 |
rs56395357 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHD3 | GRCh38.p7 | 17:7899711 | GGTACTCCCAGGGGC[A/G]TACATGGATCTGTCG | 1107 |
rs57946102 | snp | A/T | 0.0249685 | 0.108907 | intron-variant | CHD3 | GRCh38.p7 | 17:7893579 | GCAAAGGTAGGGAAC[A/T]CTCTTCCAACAACTG | 1107 |
rs58175866 | in-del | -/T | 0 | 0 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913187 | TTTTTTTTTTTTTTT[-/T]AAGGCGTTGAGGGTC | 1107 |
rs58708945 | snp | C/G | 0.0592355 | 0.161582 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7911869 | CTTCCTCCCACACTG[C/G]CAAGTATACACAACT | 1107 |
rs58869323 | snp | A/C | | | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907430 | AGAGGATGAGGTGCC[A/C]GGGGTGCCTGGAGAG | 1107 |
rs58909711 | snp | C/T | 0.292886 | 0.246294 | intron-variant | CHD3 | GRCh38.p7 | 17:7898458 | AAAGCGTAGGACTCC[C/T]AAGGATGAGGCCTCA | 1107 |
rs59090856 | snp | C/G | 0.101658 | 0.201233 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888408 | GGGCTGGGCCAAGCC[C/G]AGGCTTTCCCATCTT | 1107 |
rs59605221 | snp | A/G | 0.145642 | 0.227177 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885961 | GAACCAGATACCCCC[A/G]GCTCCACCCCCTTCA | 1107 |
rs59664969 | snp | C/T | | | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890977 | CAACTCTGCTTCTGA[C/T]CTGGGGCCTGGAGGA | 1107 |
rs60249108 | snp | G/T | 0.0498117 | 0.149749 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913036 | TGGGAGGAGCGCCTA[G/T]CAAGATTCAAAACTG | 1107 |
rs60280836 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905514 | GAGCACCTCAAACGT[A/G]ACAGGAATGTTCCTG | 1107 |
rs60424695 | snp | C/T | 0.0720551 | 0.175601 | intron-variant | CHD3 | GRCh38.p7 | 17:7907278 | GATTCCCCTGTGGAG[C/T]GGGAGGGGAGGGGGC | 1107 |
rs61738372 | snp | A/G/T | 1.65367e-05 | 0.00287543 | missense | CHD3 | GRCh38.p7 | 17:7907957 | CACGGTCCAATGGGC[A/G/T]ACGAGAGGAAAAGAC | 1107 |
rs61740589 | snp | C/T | 0.000592876 | 0.0172072 | intron-variant, missense | CHD3 | GRCh38.p7 | 17:7889067 | CTGAGGATTTCTTTT[C/T]CTCCAGGACTGTGTT | 1107 |
rs61744663 | snp | A/G | 0.00787629 | 0.0622584 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7900582 | GGGCTTCCTGGAGGA[A/G]TTTGCTGACATATCC | 1107 |
rs61744840 | snp | C/T | 0.0175067 | 0.0919068 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7903922 | AACTGAGGACACTGA[C/T]GTGCAGAACATGAAT | 1107 |
rs61745102 | snp | C/G | 0.197531 | 0.244432 | missense | CHD3 | GRCh38.p7 | 17:7897142 | GAATGACATGGATGA[C/G]CCCCCACCCCTGGAC | 1107 |
rs61746790 | snp | A/G | 0.00792551 | 0.0624495 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899154 | TGATGAGATGGGGCT[A/G]GGCAAGACCATACAA | 1107 |
rs61753145 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7900924 | TGGGAACCAGGTGTC[A/G]CTGCTTAATATCATG | 1107 |
rs61753146 | snp | G/T | 0.002354 | 0.0342266 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7902983 | GTCCACCCGAGCTGG[G/T]GGCCTGGGCATCAAT | 1107 |
rs62062522 | snp | A/C | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7891751 | CTGTAATCCCAGCTA[A/C]TCGGGAGGCTAAGGC | 1107 |
rs62062523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7897412 | TAACCTTGATAACCT[C/T]TGCTGTAGCTCCAGC | 1107 |
rs62062524 | snp | C/G | 0.365853 | 0.221536 | intron-variant | CHD3 | GRCh38.p7 | 17:7901087 | TGAGCCACAGGGGTG[C/G]AGCTGGGCTGGAAGG | 1107 |
rs68076797 | in-del | -/TG | 0.0858192 | 0.188533 | intron-variant | CHD3 | GRCh38.p7 | 17:7890050 | CAAGCTCTGGAAGAC[-/TG]TATGAATTCAAGAGT | 1107 |
rs71159531 | in-del | -/G | 0 | 0 | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912787 | TTTATGGGGGGGGGG[-/G]AGTTTTTGGGGGGAG | 1107 |
rs71359656 | in-del | -/CCAAGGATCCAGAGACAGGGATCCGTGAGGG | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7893972 | CTAAACACCTGGGGG[lengthTooLong]CCAAGGATCCAGAGA | 1107 |
rs71359657 | in-del | -/G | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7902391 | CACCACTGCACTCCA[-/G]GCTAGGGCAACAGAA | 1107 |
rs71359658 | in-del | -/C | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7908607 | AGGGCTAGTGCCACA[-/C]TTTGGGGAGTCAAGC | 1107 |
rs71359659 | in-del | -/A | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7909387 | CCCACAACGCTGCGT[-/A]AGTCTTCACCCCGCA | 1107 |
rs71359660 | in-del | -/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7909389 | ACAACGCTGCGTAAG[-/T]TCTTCACCCCGCACC | 1107 |
rs72635515 | snp | A/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7909553 | TGTCTGATAGCATTC[A/C]CATCCGTGCCCAATA | 1107 |
rs72841432 | snp | C/T | 0.103794 | 0.20279 | intron-variant | CHD3 | GRCh38.p7 | 17:7889980 | TTCACTGCAACCTAG[C/T]GAAGAGCCTCGTTGT | 1107 |
rs72841437 | snp | C/G/T | 0.0404685 | 0.136369 | intron-variant | CHD3 | GRCh38.p7 | 17:7909429 | CTTCCCACCCCCTGA[C/G/T]CCCTCTACCTGCTGA | 1107 |
rs73233646 | snp | A/G | 0.180383 | 0.240111 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7882863 | CTCCTGAGCACCGCC[A/G]AAGATGGGTGGCCAG | 1107 |
rs73233656 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | CHD3 | GRCh38.p7 | 17:7903730 | GAAAAAGCCTTCTCT[A/G]GGGCTCCTGTGAAAA | 1107 |
rs73977776 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CHD3 | GRCh38.p7 | 17:7900218 | GCTGGGGCAGGGAAA[A/G]GCTGATGCTGTGGGT | 1107 |
rs73977777 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CHD3 | GRCh38.p7 | 17:7901064 | GGGAGTAGTGGGGAG[A/G]TGGGTATTGAGCCAC | 1107 |
rs73977778 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CHD3 | GRCh38.p7 | 17:7902808 | GATGGGAGGGGGACT[A/G]GCTTGGGGGACATTG | 1107 |
rs73977779 | snp | A/G | 0.030665 | 0.119967 | intron-variant | CHD3 | GRCh38.p7 | 17:7903577 | TCAGCCCCCTGGGGA[A/G]AGAAAAACAACTCTT | 1107 |
rs74468381 | snp | C/T | 0.0329836 | 0.124112 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888125 | GCTGCTGGGGCATGG[C/T]GCCTTCCTTGCTGAC | 1107 |
rs74514789 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7887444 | AATAATATAACATAA[C/T]ATATAGATGTGATTC | 1107 |
rs74605012 | snp | G/T | 0.0916144 | 0.193427 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885916 | ACAGCAGTCCATTCG[G/T]ATTGGGGAGCGGAGA | 1107 |
rs74903197 | snp | C/T | 0.00724717 | 0.0597584 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903028 | CACTGTCATCATCTT[C/T]GATTCTGACTGGAAC | 1107 |
rs74948151 | snp | C/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7896406 | TTTTTCTTTTTTTTT[C/T]TATTTTTTTTTTTTT | 1107 |
rs74964036 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885744 | GGAGACTTAGGTGCC[C/G]GCCAACTGAGGGGCA | 1107 |
rs75122325 | snp | A/G | 0.045981 | 0.144486 | intron-variant | CHD3 | GRCh38.p7 | 17:7893947 | CTCGGTGAGTGACCC[A/G]TCCCTGTCTACTAAA | 1107 |
rs75272065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7901838 | TCTTAAGGTTGCTGG[A/G]AGTTGAGGTCCAGCT | 1107 |
rs75299897 | snp | G/T | 0.5 | 0 | missense, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903021 | CTGCTGACACTGTCA[G/T]CATCTTTGATTCTGA | 1107 |
rs75678869 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | CHD3 | GRCh38.p7 | 17:7889844 | AGAGACCTACATTTT[C/T]TCTGGTCCTGATTAC | 1107 |
rs76447710 | snp | C/T | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7896403 | TCCTTTTTCTTTTTT[C/T]TTCTATTTTTTTTTT | 1107 |
rs76629318 | snp | C/T | 0.5 | 0 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913172 | GCAAAGGCACACTTT[C/T]TTTTTTTTTTTTTTT | 1107 |
rs77030672 | snp | G/T | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7892514 | TTTTTTTTTTTTTTT[G/T]TGAGATGGAATCTCA | 1107 |
rs77130794 | snp | C/T | 0.000389286 | 0.013946 | intron-variant | CHD3 | GRCh38.p7 | 17:7899574 | TCATATCCTCTGAGA[C/T]CCTCAAAGCTGTCAC | 1107 |
rs77526752 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904293 | TGGCATGGAACATGC[G/T]CAATGTCCAGAAAAT | 1107 |
rs78044421 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886820 | TGGAGTCTGGGGTGG[A/G]GTGGTGTGGGTCCCG | 1107 |
rs78094615 | snp | A/T | 0.5 | 0 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913171 | AGCAAAGGCACACTT[A/T]TTTTTTTTTTTTTTT | 1107 |
rs78576661 | snp | A/G | | | synonymous-codon, intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7884938 | CGACGAGGACGATGA[A/G]GAGGACGACGACGAG | 1107 |
rs78578802 | snp | G/T | 0.5 | 0 | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912795 | GGGGGGGGAGTTTTT[G/T]GGGGGAGGGATAAGA | 1107 |
rs78632271 | snp | A/C | 0.000175731 | 0.00937203 | intron-variant | CHD3 | GRCh38.p7 | 17:7907597 | CCCCTACCCCCTCCC[A/C]CAGCCACAGAGTCGA | 1107 |
rs78632606 | snp | A/G | 4.94629e-05 | 0.00497283 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893935 | GAAGAAAGGAGGCTC[A/G]GTGAGTGACCCGTCC | 1107 |
rs78698003 | snp | A/G/T | 0.0150606 | 0.0854603 | intron-variant | CHD3 | GRCh38.p7 | 17:7901107 | GGGCTGGAAGGCCAC[A/G/T]GACTGGGTGTCTGAG | 1107 |
rs78773765 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | CHD3 | GRCh38.p7 | 17:7893215 | GTACATAGATTTAAT[C/T]GATGAGGGGAGATGG | 1107 |
rs79342851 | snp | C/T | 0.0017602 | 0.0296143 | intron-variant | CHD3 | GRCh38.p7 | 17:7899575 | CATATCCTCTGAGAC[C/T]CTCAAAGCTGTCACT | 1107 |
rs79725220 | in-del | -/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7909552 | ATGTCTGATAGCATT[-/C]ACATCCGTGCCCAAT | 1107 |
rs79930761 | snp | C/T | 0.0448719 | 0.142907 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912394 | AGATGTGGTGGAAGC[C/T]CAGCTCTGGGGCTCA | 1107 |
rs79977412 | snp | C/T | 1.64974e-05 | 0.00287201 | missense | CHD3 | GRCh38.p7 | 17:7899045 | CTCAGCCACGGTTTA[C/T]CACAGCCACTGGAGG | 1107 |
rs80199415 | snp | A/G | | | missense | CHD3 | GRCh38.p7 | 17:7908004 | ATGTTCAATATCGCC[A/G]ATGGTGGCTTCACAG | 1107 |
rs111368246 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904955 | CCAAGTCAGACTTTG[G/T]GCAGTGATCTGGTGT | 1107 |
rs111435916 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883834 | CCTTCTGAAGTATTC[-/A]AAAAAAAAAAAGCTT | 1107 |
rs111436114 | snp | A/G | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7893703 | AGTGGGGCTTAGTGA[A/G]ACCACAGCCCACAGA | 1107 |
rs111630031 | snp | A/G | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885955 | TCTGGGGAACCAGAT[A/G]CCCCCGGCTCCACCC | 1107 |
rs111670930 | snp | A/G | 0.5 | 0 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7903958 | TCTCAGCTCCTTCAA[A/G]GTGGCACAGTACGTC | 1107 |
rs111897016 | snp | C/T | 1.65704e-05 | 0.00287836 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899025 | GCCTACCGTGAAATA[C/T]GAGACTCAGCCACGG | 1107 |
rs111905821 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886183 | TTCTGCAGCTTGACC[A/G]TCACTCAGCACCCGT | 1107 |
rs112052778 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885132 | GAGTGGGAGCCGCGG[A/G]CGCGCGAAGCCGGGC | 1107 |
rs112056352 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903218 | GCAGCTCTATGGGCA[C/G]CTTCTCCCCGGCCAC | 1107 |
rs112260369 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884394 | GCGCCCCCCTCAGAA[C/T]TTAAATATATTTAAA | 1107 |
rs112385500 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906744 | GCTGGCTGCCTAGTC[C/T]CTGTCCTTCCTCTGC | 1107 |
rs112386947 | snp | A/G/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7897759 | GAGGGATCTCCAGGA[A/G/T]TGTTTTGTGATAGCT | 1107 |
rs112421907 | in-del | -/A/AA | 0.404166 | 0.202048 | intron-variant | CHD3 | GRCh38.p7 | 17:7908558 | TTCTCTCAAGCTGGC[-/A/AA]AAAAAAAAAAAAGAT | 1107 |
rs112465235 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904314 | TCCAGAAAATGTATG[C/T]AGAGCCACGAAGCTG | 1107 |
rs112540267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7907771 | GGAGTCTGGGGAACC[A/G]AATGCTTGGGTCCTG | 1107 |
rs112565344 | snp | A/G | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7898427 | GGGAAGTAGGTCTGG[A/G]ATGGGTTCAGAAAAG | 1107 |
rs112656164 | snp | G/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7909057 | AGCAGTGAGGGCAGG[G/T]TGGGTCTCTTGCTAT | 1107 |
rs112781303 | snp | C/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7896799 | GAGTATCTGGGATTA[C/T]AGGCGTGCGCCACCA | 1107 |
rs112787486 | in-del | -/TG | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7898387 | GGGAAAAAGGAAATA[-/TG]GGAAAATCTAGGTCA | 1107 |
rs112859347 | snp | A/G | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7901954 | GCAGGTGAGGGTGAA[A/G]GGCACAGACCCTTTG | 1107 |
rs112872102 | snp | A/G | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7898304 | GCTGAGTAGTGGAGA[A/G]GAGGATGTTCAAGAG | 1107 |
rs112896522 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888994 | TGTGGAGACTTTCTC[C/T]TGTGTGATGAAGGCG | 1107 |
rs112904911 | snp | C/T | 0.5 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7908085 | TCATGGGGTTTCTCG[C/T]TTTGCCTGAGGCTTC | 1107 |
rs113105270 | snp | A/G | | | splice-donor-variant | CHD3 | GRCh38.p7 | 17:7898103 | CTACTGGAGACACCG[A/G]TGAGGGAATGAGCTT | 1107 |
rs113422745 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CHD3 | GRCh38.p7 | 17:7891186 | CACGGTGTATACACA[C/T]CAAATTCTACACGTC | 1107 |
rs113677362 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | CHD3, SCARNA21 | GRCh38.p7 | 17:7906242 | GGAGCCTCTCCTGGG[C/T]TGTCCTAGCCTCACA | 1107 |
rs113727925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889383 | GGACCTGCCACAGTC[A/G]GAGCCCATGGCCTGG | 1107 |
rs113757126 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CHD3, NAA38 | GRCh38.p7 | 17:7887040 | TCAGCCCTCCAAGTC[A/G]AATGAGTGACCCAGA | 1107 |
rs113777117 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHD3 | GRCh38.p7 | 17:7896680 | AAAGTGCTGGGACGC[A/G]CCTGTTATTCTCTTA | 1107 |
rs113832543 | snp | A/G | 0.000123195 | 0.00784744 | intron-variant | CHD3 | GRCh38.p7 | 17:7903781 | CCCATCAGCCTTTCT[A/G]AACTTTGGAACCCAA | 1107 |
rs114279001 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | CHD3 | GRCh38.p7 | 17:7897686 | CAATGCTGCCTTCCC[C/G]ACGAGACTCTGAGTT | 1107 |
rs114413722 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905323 | TATTCATAGTCTCTC[C/T]GCTAGTAAACTTCGG | 1107 |
rs114643514 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | CHD3 | GRCh38.p7 | 17:7903742 | TCTAGGGCTCCTGTG[A/T]AAAGGACGCAGAGTA | 1107 |
rs114765115 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CHD3 | GRCh38.p7 | 17:7895694 | TGCTTAGTTTCCATA[C/T]GTGGTTCTTTTGGTC | 1107 |
rs114797491 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | CHD3 | GRCh38.p7 | 17:7890881 | GGTAGACAGGCCTGT[G/T]TGCGGCCTGGAATAG | 1107 |
rs114834229 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CHD3 | GRCh38.p7 | 17:7889590 | AACTGCCGAGGTGGG[A/G]AAGGGGCAAGTTGAG | 1107 |
rs115087532 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CHD3 | GRCh38.p7 | 17:7894040 | TCCGTGAGGGATGGC[A/G]GAACAGGAAGCCAAA | 1107 |
rs115219924 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7887968 | GGGGAGTAGAGTGAA[A/C]CGGCTTGTGCACCAC | 1107 |
rs115334096 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CHD3 | GRCh38.p7 | 17:7897597 | GACATAATTCATCCA[A/G]ACCAGTGTTTTGAAT | 1107 |
rs115409358 | snp | C/G | 0.0027884 | 0.0372347 | intron-variant | CHD3 | GRCh38.p7 | 17:7910604 | CCGGTAACCCTCTTT[C/G]CCCCTAGCTCCAGTT | 1107 |
rs115710642 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CHD3 | GRCh38.p7 | 17:7902340 | GGCGGTAGGATCACT[G/T]GAACCCAGGAGTGGA | 1107 |
rs115770479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892363 | AGAGTATTATTGTGA[A/G]GACAAGATAAGGTGG | 1107 |
rs116087083 | snp | A/G | 0.00123398 | 0.0248086 | synonymous-codon, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890654 | ATATGGAACCGGACC[A/G]GGTCGGAAACGAAGA | 1107 |
rs116578639 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CHD3 | GRCh38.p7 | 17:7901068 | GTAGTGGGGAGGTGG[A/G]TATTGAGCCACAGGG | 1107 |
rs116657393 | snp | A/G | 0.0752113 | 0.178743 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912276 | GACCACCCCTACAAA[A/G]AGAGTAATGGTTGGG | 1107 |
rs116669040 | snp | C/T | 3.32629e-05 | 0.00407803 | intron-variant | CHD3 | GRCh38.p7 | 17:7904000 | AGACAAGGTGAGAGG[C/T]TTTGGGGGCCAGACA | 1107 |
rs116670269 | snp | A/C/T | 0.00116828 | 0.0241413 | intron-variant | CHD3 | GRCh38.p7 | 17:7894100 | CCTCACTGACGGCCA[A/C/T]GGGGCTATGGGCAGT | 1107 |
rs116976313 | snp | C/T | 0.000617722 | 0.0175636 | intron-variant | CHD3 | GRCh38.p7 | 17:7910801 | CAGCTTCTTTCCTCT[C/T]ACAGACTATGAACTA | 1107 |
rs117025212 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CHD3 | GRCh38.p7 | 17:7901861 | GTCCAGCTCTAGTTC[C/T]TTTTCAGCTGCATGA | 1107 |
rs117032670 | snp | A/G | 0.034428 | 0.126605 | intron-variant | CHD3 | GRCh38.p7 | 17:7904120 | TCAAACAACTTCTTC[A/G]TCTAATAGGTGAGAC | 1107 |
rs117163045 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | CHD3 | GRCh38.p7 | 17:7893065 | CATGAGCCACCGTGC[C/T]TGGCCTGTATTTCTT | 1107 |
rs117214580 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CHD3 | GRCh38.p7 | 17:7910704 | AACTTGCTAGAACAC[A/G]GTCATCACCCTTGAG | 1107 |
rs117471130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7909911 | GTGTAGTCACTGACT[C/T]CTGGCCCCTTTGATC | 1107 |
rs117629638 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | CHD3 | GRCh38.p7 | 17:7911350 | CTTCCCTCCCTCACG[C/T]GGGACAACGGGAAGT | 1107 |
rs117801679 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CHD3 | GRCh38.p7 | 17:7909958 | GAATCTGTAATACTG[A/G]CCTTCTAACCTCCCT | 1107 |
rs118079592 | snp | A/G | 0.0323392 | 0.122979 | synonymous-codon, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905119 | CCAGTCAGAGTACTC[A/G]GTGGGTTCAGAGGAG | 1107 |
rs138049928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889357 | AGGAGGAGCCCTGGC[A/G]GTGACTGAAAGGACC | 1107 |
rs138058125 | snp | G/T | 1.64846e-05 | 0.0028709 | missense | CHD3 | GRCh38.p7 | 17:7911511 | AAGGAGAAGGAAATG[G/T]TGGGGGCATTGGTGT | 1107 |
rs138253055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905374 | AGATCCAGAAAGGCC[A/G]TATCATTTTCCATTC | 1107 |
rs138264899 | snp | A/C | 0.000153988 | 0.00877327 | missense | CHD3 | GRCh38.p7 | 17:7893494 | GCACCCTCCGGACCC[A/C]CCGCCCTTCCACCAC | 1107 |
rs138276799 | snp | C/T | 0.000263635 | 0.0114782 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7898070 | GAATATCCCTGAATA[C/T]GAAGAACATAAGCAA | 1107 |
rs138306277 | snp | A/G | 6.17443e-05 | 0.00555593 | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890649 | AGTGAATATGGAACC[A/G]GACCGGGTCGGAAAC | 1107 |
rs138403330 | in-del | -/GAG | 0.0150606 | 0.0854603 | intron-variant | CHD3 | GRCh38.p7 | 17:7901483 | TCTGGTGTGACAAAT[-/GAG]GAGATTCCTCCTGTA | 1107 |
rs138539483 | snp | A/G | 0.00392401 | 0.0441204 | missense | CHD3 | GRCh38.p7 | 17:7894218 | CTGATGGCCCTGTCC[A/G]CACCAAGAAACTAAA | 1107 |
rs138582040 | snp | A/G | 3.32768e-05 | 0.00407888 | intron-variant | CHD3 | GRCh38.p7 | 17:7898131 | CTTGTGGATTCAAGG[A/G]ATTCTGACGATGAGG | 1107 |
rs138752707 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904458 | TTGAGGAAATTGAGC[A/G]AGAGATCATCAAGCA | 1107 |
rs138878893 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890976 | GCAACTCTGCTTCTG[A/G]CCTGGGGCCTGGAGG | 1107 |
rs138883221 | snp | C/G/T | 1.66181e-05 | 0.00288249 | CHD3, SCARNA21 | 17 | allele_origin=G(somatic)/C(germline) | 17:7906647 | CGGGAGGGACTGAGT[C/G/T]GCCAGCAGGTGTTGA | 1107 |
rs138884047 | in-del | -/G | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884162 | AAAAAGGAGAAATTT[-/G]TGGGTTTCTGGGTAA | 1107 |
rs138945661 | snp | A/G | 0.00016856 | 0.00917887 | missense | CHD3 | GRCh38.p7 | 17:7910925 | GTAGGGGCCCTGGCC[A/G]CCGCAGGCGCCAATT | 1107 |
rs138976937 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | CHD3 | GRCh38.p7 | 17:7897170 | GACTATGGCTCCGGC[A/G]AGGATGATGGGAAGA | 1107 |
rs139167725 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CHD3 | GRCh38.p7 | 17:7902341 | GCGGTAGGATCACTT[C/G]AACCCAGGAGTGGAG | 1107 |
rs139173826 | snp | A/G | 0.000164745 | 0.00907442 | missense | CHD3 | GRCh38.p7 | 17:7893853 | GAGTGCCTGATGGAC[A/G]CAAGAAGCTTCGGGG | 1107 |
rs139259477 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CHD3 | GRCh38.p7 | 17:7895704 | CCATATGTGGTTCTT[C/T]TGGTCTACAGTCCTC | 1107 |
rs139484082 | snp | C/G | 0.000329783 | 0.0128368 | missense | CHD3 | GRCh38.p7 | 17:7907194 | GAGGAAGCTGAAAAC[C/G]AGGAGGAAAAGCCAG | 1107 |
rs139543333 | in-del | -/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7911460 | TACCCCTTTCCCAAA[-/C]CAGCCGCCACCAACG | 1107 |
rs139555974 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | CHD3 | GRCh38.p7 | 17:7908159 | ATGCTGACTCCGATC[A/C]TTGCTCTAAATCTTT | 1107 |
rs139741951 | snp | C/G | 6.85883e-05 | 0.00585572 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907364 | CCAGGCTGATGCCCC[C/G]AGCCCAGCCCCATCA | 1107 |
rs139963970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886469 | TCTTTGTAAAACTGT[C/G]ATATTGATCCGTGTG | 1107 |
rs140009880 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CHD3 | GRCh38.p7 | 17:7902032 | CAATGACACAATTTT[G/T]TACGGATTTTCAGGG | 1107 |
rs140028202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905791 | CTGGATCACTGAAGG[C/T]AGAAAGGACAAGACC | 1107 |
rs140053077 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CHD3, NAA38 | GRCh38.p7 | 17:7887003 | ACCTCCCCTCTCCCC[C/T]TGGGCAATTTTTATC | 1107 |
rs140212883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7893192 | TCACCACCCAGGAAT[C/T]CTAGCATGTACATAG | 1107 |
rs140448992 | snp | C/T | 0.000183448 | 0.00957551 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910890 | CTCCGGGGTACGGGG[C/T]GGCCTTCAGCGCCGC | 1107 |
rs140550382 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899934 | TGTTCTCCTGACATC[A/G]TATGAGCTGATCACC | 1107 |
rs140662047 | snp | C/T | 0.00144875 | 0.0268752 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897190 | TGATGGGAAGAGCGA[C/T]AAGCGTAAAGTGAAA | 1107 |
rs140669112 | snp | A/G | 0.000181676 | 0.00952915 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903424 | TGGGCTGGGCTCCAA[A/G]GCAGGCTCCATGTCC | 1107 |
rs140749039 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7897554 | GCACATGAGTCTGGG[G/T]ATGAGGGCATGAAAG | 1107 |
rs140795591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7891288 | GTGGAGGGGCCATCA[C/T]GATTCCAGTGCTGGG | 1107 |
rs140885794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7894743 | AGTGTCTAGGATCCT[A/G]ATGTATTCCTTTCTC | 1107 |
rs141057316 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | CHD3 | GRCh38.p7 | 17:7892784 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTATTT | 1107 |
rs141080506 | snp | A/G | 6.58989e-05 | 0.00573978 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7895066 | CCTGTGCTGTGACGC[A/G]TGCATCTCCTCCTAC | 1107 |
rs141097658 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | CHD3 | GRCh38.p7 | 17:7896529 | TCCTGCCTCAGCCAC[C/T]CAAGTAGCTGGGATT | 1107 |
rs141138068 | snp | A/G | 3.33678e-05 | 0.00408446 | missense | CHD3 | GRCh38.p7 | 17:7894929 | TAGGAGAAGGAGGGG[A/G]TCCAGTGGGAGGCCA | 1107 |
rs141170392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910186 | CTTTCTCTCCATCTG[C/T]CTTCTGTGGTAATCT | 1107 |
rs141519608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886074 | GCTGCCCAGCTGTGA[C/T]TCTCACGTGGCTGCC | 1107 |
rs141535644 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904745 | CCTCTGCTAAAAGGG[A/G]AAGACATAAGGTAGA | 1107 |
rs141550862 | snp | A/G | 6.60262e-05 | 0.00574532 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7911554 | ATCGGAAGGAGCCCC[A/G]AGCCGGGGAGGTGAT | 1107 |
rs141560724 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CHD3 | GRCh38.p7 | 17:7890025 | CAGCAAAGAGAAGCA[A/G]TTGAAAGCACAAGCT | 1107 |
rs141586164 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD3 | GRCh38.p7 | 17:7890291 | CAAAAATCAGCCGGG[C/T]GCGGTGGTACGTCTG | 1107 |
rs141697841 | snp | C/T | 0.0011372 | 0.0238182 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7906934 | GCCTGACCCCAGCGC[C/T]GATTCTAAGCGCTCC | 1107 |
rs141804435 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899345 | TCTTGACTCCCAGGG[C/T]CACACAAAAGGTCCC | 1107 |
rs141834994 | snp | C/T | 0.000934673 | 0.0215978 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893496 | ACCCTCCGGACCCCC[C/T]GCCCTTCCACCACCC | 1107 |
rs141945730 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906063 | TTTCTTCCTTGGGGC[C/T]GCCATATGATGTGAC | 1107 |
rs142036457 | in-del | -/C | 0.0460142 | 0.144533 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912456 | CTCAAGGCCTGGATA[-/C]AGACTAAATTTGTAT | 1107 |
rs142074961 | snp | A/G | 1.69438e-05 | 0.00291061 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893352 | CATCCTTGGGGCCAA[A/G]TGGAGAGAGTTCAGT | 1107 |
rs142170880 | in-del | -/GGGG | | | frameshift-variant, intron-variant | CHD3 | GRCh38.p7 | 17:7895384 | TCCTACATTGGCGGT[-/GGGG]GGGGGGAGCCACCTG | 1107 |
rs142373217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888348 | GTGGCTAATTTTCCG[C/T]TGGCTGTTGAGGGAA | 1107 |
rs142481394 | snp | C/T | 1.64958e-05 | 0.00287187 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7902628 | ACCAAAATGTTAGAC[C/T]TGCTTGAGGACTTCT | 1107 |
rs142513753 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CHD3 | GRCh38.p7 | 17:7889437 | GGGGAGGGAGGGGAG[C/T]GGTTTGGCTGCTCTT | 1107 |
rs142635953 | snp | A/G | 0.000217988 | 0.0104377 | intron-variant | CHD3 | GRCh38.p7 | 17:7907515 | GCCTTAGGAGTGATG[A/G]GGGATTAGAATTTGG | 1107 |
rs142695071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892400 | TGTGAAAGGGTTTTA[G/T]GAACTGTAAAGTAGT | 1107 |
rs142798308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901693 | TTTTTGTATTTTTAG[C/T]AGAGACGGGATTTCA | 1107 |
rs142817060 | snp | A/G | 3.29788e-05 | 0.00406058 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7906871 | CCTGCCACCCCAGGT[A/G]CAGGAGTTTGAGCAC | 1107 |
rs142874934 | snp | A/G | 0.00111919 | 0.0236293 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905585 | AGGCTTAGAGGAGGT[A/G]GTGGCTCAGCTAACT | 1107 |
rs142929440 | snp | C/T | 3.36995e-05 | 0.00410471 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910927 | AGGGGCCCTGGCCGC[C/T]GCAGGCGCCAATTAC | 1107 |
rs143090817 | in-del | -/AG | 0.00847076 | 0.0645262 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904649 | GATGCAGGCAGTAAA[-/AG]GGGGGGAAGTGATGA | 1107 |
rs143122467 | snp | A/C | 3.29897e-05 | 0.00406125 | missense | CHD3 | GRCh38.p7 | 17:7907202 | TGAAAACCAGGAGGA[A/C]AAGCCAGAGAAGAAC | 1107 |
rs143237578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888531 | GGTCTGTGGGGCATC[C/T]TGTCTTCCTTTATGT | 1107 |
rs143311941 | snp | C/T | 0.000337137 | 0.012979 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908003 | CATGTTCAATATCGC[C/T]GATGGTGGCTTCACA | 1107 |
rs143327592 | snp | A/G | 6.64091e-05 | 0.00576196 | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890680 | GAAGAAGGAAGCACC[A/G]AGAAAAAAAGGAGAA | 1107 |
rs143485678 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | CHD3 | GRCh38.p7 | 17:7902186 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAAGATCA | 1107 |
rs143501783 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CHD3 | GRCh38.p7 | 17:7897001 | TCCCTGTCCCATTCC[C/T]CCTGCCGGCCTCTTC | 1107 |
rs143802807 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | CHD3 | GRCh38.p7 | 17:7911209 | TTGGTGTCTTCTACC[A/C]GAGCCACCTCCCTCC | 1107 |
rs143956989 | snp | A/G | 3.29772e-05 | 0.00406048 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7911522 | AATGGTGGGGGCATT[A/G]GTGTCAGACGGGCTG | 1107 |
rs143999586 | snp | C/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7894156 | TGAACCAGAGGCTGA[C/G]GAATCAGACCTGGAC | 1107 |
rs144025099 | snp | A/G | 1.66092e-05 | 0.00288172 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894440 | TCCTGCAGTGGCCGG[A/G]GAGGAGGAGGTTGAT | 1107 |
rs144116093 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7898217 | CTGGAGTTCAGGGCA[A/G]TGGCCACCTGAGCTG | 1107 |
rs144309626 | snp | A/G | 1.7232e-05 | 0.00293525 | missense | CHD3 | GRCh38.p7 | 17:7908458 | TCCTCGGGGAAACTC[A/G]ATGAGATCTGGCACA | 1107 |
rs144356754 | snp | A/G | 4.94328e-05 | 0.00497131 | missense | CHD3 | GRCh38.p7 | 17:7894535 | GTGACACCTGCCCTC[A/G]TGCCTACCACCTCGT | 1107 |
rs144370104 | snp | A/G | 0.000510662 | 0.0159709 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7900349 | GCTGACAGGAACCCC[A/G]TTGCAGAATAATCTG | 1107 |
rs144413508 | snp | G/T | 0.00294535 | 0.0382623 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907436 | TGAGGTGCCAGGGGT[G/T]CCTGGAGAGATGGAG | 1107 |
rs144433709 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7890075 | CAAGAGTCCAGCATT[C/T]CTCTGTCTAGGATAC | 1107 |
rs144649037 | snp | C/T | 0.00213357 | 0.0325919 | intron-variant, nc-transcript-variant | CHD3, SCARNA21 | GRCh38.p7 | 17:7906155 | GGTGGTCTCAGCCCA[C/T]TCCACCTCCCCTCAG | 1107 |
rs144713021 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | CHD3 | GRCh38.p7 | 17:7889867 | CTGATTACTGGTGTG[G/T]GGGTGGGGTTCTGAA | 1107 |
rs144741806 | in-del | -/G | 0.446118 | 0.155041 | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912778 | TCTGTTATTTTTTAT[-/G]GGGGGGGGGAGTTTT | 1107 |
rs144753161 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CHD3 | GRCh38.p7 | 17:7892839 | ATTCTGTCACCCAGG[C/T]TGCACTGCAGTGGTG | 1107 |
rs144755542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHD3 | GRCh38.p7 | 17:7901434 | CTCTCCTCATCCTCC[A/G]GACTTTAATTTCTTA | 1107 |
rs144911273 | snp | A/G | 0.00026541 | 0.0115167 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7901297 | GGCACTTATTAAGTC[A/G]TCTGGGAAGCTCATG | 1107 |
rs144962853 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHD3 | GRCh38.p7 | 17:7902510 | AGGGCAGGGGTTCAG[A/G]TGTAAAGATTAGGGT | 1107 |
rs145306324 | in-del | -/TCCGTGAGGGCCAAGGATCCAGAGACAGGGA | | | intron-variant | CHD3 | GRCh38.p7 | 17:7893994 | TCCAGAGACAGGGAT[lengthTooLong]CCGTGAGGGCCAAGG | 1107 |
rs145717741 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7892206 | CTCAGCACCATGGAT[C/T]ACCCGTGTCCGCACA | 1107 |
rs145734007 | snp | A/G | 9.88549e-05 | 0.00702977 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7898022 | ATGGAGGGACTTACC[A/G]TATGACCAGTCCACG | 1107 |
rs145746966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7897893 | TTTGCTGATAATTGC[A/G]TTTCTCAGGCCTTCT | 1107 |
rs145820212 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886608 | CTCCCCGCCCCCCAA[A/G]CTTGTCTGAAAAAGG | 1107 |
rs145839343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7903598 | AACAACTCTTCTCTG[C/T]AGCCTTTGAAGGAAG | 1107 |
rs145883027 | snp | C/T | 0.00333321 | 0.0406878 | intron-variant | CHD3 | GRCh38.p7 | 17:7910418 | TCTTTCTCTGTGGCC[C/T]GGGCCCCAGTTCTGA | 1107 |
rs146064624 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CHD3 | GRCh38.p7 | 17:7901713 | ACGGGATTTCACCAT[A/G]TTGGTCAGGATGGTC | 1107 |
rs146077055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905588 | CTTAGAGGAGGTGGT[A/G]GCTCAGCTAACTGAT | 1107 |
rs146189491 | snp | C/T | 0.000230601 | 0.0107353 | synonymous-codon, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905149 | GGAGGATGAAGACTT[C/T]GATGAACGTCCTGAA | 1107 |
rs146326109 | snp | C/G | 0.000307953 | 0.0124049 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893484 | CACCCCCATAGCACC[C/G]TCCGGACCCCCCGCC | 1107 |
rs146352528 | in-del | -/CT | 0.182933 | 0.240836 | intron-variant | CHD3 | GRCh38.p7 | 17:7896221 | CGACAGAGCGACACT[-/CT]ATCTCAAAAAAAAAA | 1107 |
rs146525126 | snp | A/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896387 | ATTTATCTCTAATCC[A/T]TCCTTTTTCTTTTTT | 1107 |
rs146583144 | snp | A/G | 0.000148323 | 0.00861042 | missense | CHD3 | GRCh38.p7 | 17:7903867 | TGATTCATTATGACA[A/G]TGAGGCCATCGCTCG | 1107 |
rs146616544 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907613 | CAGCCACAGAGTCGA[C/T]GCCAGGAGAAAGGGG | 1107 |
rs146731360 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CHD3 | GRCh38.p7 | 17:7896721 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCGCTG | 1107 |
rs146742892 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CHD3 | GRCh38.p7 | 17:7902229 | AGTTTCAAGACCAGC[C/T]TGGCCAACATGGTGA | 1107 |
rs146879057 | snp | A/G | 1.65012e-05 | 0.00287234 | missense | CHD3 | GRCh38.p7 | 17:7907224 | GAGAAGAACAGCAGA[A/G]TTGGGGAGAAGATGG | 1107 |
rs146907233 | snp | C/T | 3.38524e-05 | 0.00411401 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904420 | GAGACCCCCAGTGTT[C/T]ATTCATTCTGTTGCC | 1107 |
rs146930588 | snp | A/C | 0.0295025 | 0.117817 | intron-variant | CHD3 | GRCh38.p7 | 17:7910320 | TGTTCTCCTCTCTCG[A/C]TCTTTTTCTGCCTGT | 1107 |
rs147004540 | snp | C/T | 8.24069e-05 | 0.00641846 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7911479 | CCGCCACCAACGGCC[C/T]TCCAGTGCTTGTGAA | 1107 |
rs147218672 | snp | C/T | 0.000197749 | 0.0099416 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899925 | GAAGTTCCATGTTCT[C/T]CTGACATCGTATGAG | 1107 |
rs147295717 | snp | C/T | 0.00165949 | 0.0287575 | intron-variant | CHD3 | GRCh38.p7 | 17:7894631 | CCTAATGCCAGCATC[C/T]GATGGCCCTGAGGAA | 1107 |
rs147318467 | snp | A/T | 4.98409e-05 | 0.00499179 | intron-variant | CHD3 | GRCh38.p7 | 17:7898485 | CTCATTCAGACCCAC[A/T]CTTTTTCCAGAGAAC | 1107 |
rs147380106 | snp | C/T | 4.95872e-05 | 0.00497907 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7900573 | CAACTTGGAGGGCTT[C/T]CTGGAGGAGTTTGCT | 1107 |
rs147395786 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | CHD3 | GRCh38.p7 | 17:7906891 | AGTTTGAGCACATCA[A/G]TGGGCGTTGGTCAAT | 1107 |
rs147547238 | snp | C/T | 4.96463e-05 | 0.00498203 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894132 | TGTTTTTCAGAGCGA[C/T]GAAGGTCCTGAACCA | 1107 |
rs147683463 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7887922 | TCCCGCCACCGACGC[C/T]TGCCCAAGTTCGGGA | 1107 |
rs147787289 | snp | A/G | 3.32995e-05 | 0.00408027 | intron-variant | CHD3 | GRCh38.p7 | 17:7908865 | GAGCGGGTTATAGAC[A/G]GGCTTGGGTCAGAAG | 1107 |
rs147796138 | snp | A/G | 0.000116031 | 0.00761592 | missense | CHD3 | GRCh38.p7 | 17:7894574 | ATCCTGAGCTTGACC[A/G]GGCTCCAGAGGGCAA | 1107 |
rs148004601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7897541 | GGCATAAGACATAGC[A/G]CATGAGTCTGGGGAT | 1107 |
rs148016968 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883436 | CCAAATTAATTTCTC[A/G]AGTCAGTTGAATTTT | 1107 |
rs148141006 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7911972 | TCATGTGGAAGTGGA[G/T]AATCAGCCTTGCCTG | 1107 |
rs148374688 | snp | A/C | 1.87009e-05 | 0.00305779 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904657 | GCAGTAAAGGGGGGA[A/C]GTGATGATGAGTAGG | 1107 |
rs148393036 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | CHD3 | GRCh38.p7 | 17:7890202 | TTGGGAGGCTGAGCC[A/G]GGTAGATCATTTGAG | 1107 |
rs148451716 | snp | A/G | 0.000329739 | 0.0128359 | missense | CHD3 | GRCh38.p7 | 17:7906932 | ATGCCTGACCCCAGC[A/G]CCGATTCTAAGCGCT | 1107 |
rs148476518 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7906776 | TCTGTCCCTGAGTTG[G/T]AAGCTTGCGCTGGTG | 1107 |
rs148614032 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | CHD3 | GRCh38.p7 | 17:7910270 | TTTTCCATCTACTTC[-/T]TTTACTTTCTTGATC | 1107 |
rs148625731 | snp | A/G | 0.00034636 | 0.0131552 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7911542 | CAGACGGGCTGGATC[A/G]GAAGGAGCCCCGAGC | 1107 |
rs148863706 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CHD3 | GRCh38.p7 | 17:7896821 | GCGCCACCACACCTG[A/G]CTAATTTCTGTATTT | 1107 |
rs148921853 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHD3 | GRCh38.p7 | 17:7892228 | GTCCGCACAAGAGTT[A/G]AGCACCCCACCCCAG | 1107 |
rs149027084 | snp | C/T | 0.000834021 | 0.0204038 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7901363 | AGGACACCGAGTGCT[C/T]ATCTTCTCGCAGGTG | 1107 |
rs149185282 | snp | A/G/T | 0.000897606 | 0.0211665 | missense | CHD3 | GRCh38.p7 | 17:7907912 | ATGTAAAAGGTGACC[A/G/T]GGAGCTTCGACCAGG | 1107 |
rs149257134 | in-del | -/ACAC/ACACAC | 0.438526 | 0.164189 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884071 | CTTCATGCCCCCCCA[-/ACAC/ACACAC]AACACACACACACAC | 1107 |
rs149507479 | snp | C/T | 9.89185e-05 | 0.00703203 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7911520 | GAAATGGTGGGGGCA[C/T]TGGTGTCAGACGGGC | 1107 |
rs149562838 | snp | A/G | 0.000758137 | 0.0194549 | missense | CHD3 | GRCh38.p7 | 17:7899056 | TTTATCACAGCCACT[A/G]GAGGCACCCTGCACA | 1107 |
rs149781894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7891885 | AAAAAAGAAAAAATA[A/G]TGCCGATGTATTTTG | 1107 |
rs149882575 | snp | C/T | 6.59652e-05 | 0.00574267 | missense | CHD3 | GRCh38.p7 | 17:7900725 | TGGAGCTAAGCCCCA[C/T]GCAGAAGTAAGATGC | 1107 |
rs149936335 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | CHD3 | GRCh38.p7 | 17:7893865 | GACGCAAGAAGCTTC[A/G]GGGAAAGAAAATGGC | 1107 |
rs149982310 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CHD3 | GRCh38.p7 | 17:7895964 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 1107 |
rs150214574 | snp | C/G | 1.64784e-05 | 0.00287035 | missense | CHD3 | GRCh38.p7 | 17:7903948 | TGAATGAGTATCTCA[C/G]CTCCTTCAAGGTGGC | 1107 |
rs150267300 | snp | C/T | 0.000395322 | 0.0140536 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897169 | GGACTATGGCTCCGG[C/T]GAGGATGATGGGAAG | 1107 |
rs150451541 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905260 | AAGTAAAAAAGTCTT[C/T]GTGTGTGTGTGGAAA | 1107 |
rs150535094 | snp | C/G | 0.000264393 | 0.0114946 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907006 | TGAGGCTTCTGCTAC[C/G]AACAGTCCCTGCACC | 1107 |
rs150704674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886445 | ACTTCAAAACGGCCA[A/C]CTCCGGGCTCTTTGT | 1107 |
rs150799852 | snp | A/C/G | 0.192244 | 0.243941 | missense | CHD3 | GRCh38.p7 | 17:7893497 | CCCTCCGGACCCCCC[A/C/G]CCCTTCCACCACCCC | 1107 |
rs150839047 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CHD3 | GRCh38.p7 | 17:7894834 | GCACTTCTAGGATTC[A/C]GGTGTCCTGTCTTTG | 1107 |
rs150891602 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CHD3 | GRCh38.p7 | 17:7890344 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 1107 |
rs150988632 | snp | C/T | 0.00357214 | 0.0421107 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908006 | GTTCAATATCGCCGA[C/T]GGTGGCTTCACAGGT | 1107 |
rs151122368 | snp | C/T | 0.000345915 | 0.0131468 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7895039 | CCGCGTATGCAAGGA[C/T]GGCGGGGAGCTCCTG | 1107 |
rs151230039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888786 | GTGTGTCTGTCTGTG[C/T]CTATATCTTTGTTTG | 1107 |
rs151264225 | snp | C/T | 6.73389e-05 | 0.00580215 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910590 | AGCCTCACCCCACAC[C/T]GGTAACCCTCTTTCC | 1107 |
rs180787923 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7893656 | TCTCGCCTTCCCAGC[C/T]CTGATTGCTGGAGGA | 1107 |
rs180880011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7906797 | TGCGCTGGTGTGAGA[C/T]GGAGGAGACTGGAGC | 1107 |
rs181125196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892285 | TCACACTCCGTCCTA[C/T]GGAAGCCCATCTTCA | 1107 |
rs181367150 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7909480 | AACCCCACTCCTACC[A/G]ACCTGGCACCCCCTT | 1107 |
rs181583634 | snp | A/G | 0.000436967 | 0.0147747 | intron-variant | CHD3 | GRCh38.p7 | 17:7907518 | TTAGGAGTGATGGGG[A/G]ATTAGAATTTGGGAT | 1107 |
rs181598718 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7898950 | TGCCAGGGAGGAAGA[C/G]ACTAAGACTGGAGGA | 1107 |
rs181706448 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888444 | GGCTGCCTCTCTCTG[C/T]ACTAGACAGGTCTGG | 1107 |
rs181729288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7887205 | CTTGTCTAGAGTATG[A/C]ATTTGTGCACAGGAG | 1107 |
rs181942833 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CHD3 | GRCh38.p7 | 17:7901429 | CTTCCCTCTCCTCAT[C/T]CTCCAGACTTTAATT | 1107 |
rs182112232 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | CHD3 | GRCh38.p7 | 17:7892017 | ATCCTCAATTTCCTC[C/T]TCTATAAACGGGGAA | 1107 |
rs182239876 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense | CHD3 | GRCh38.p7 | 17:7911586 | TGTATAGACGACTGA[C/G]TGGATCCCAGGCCTG | 1107 |
rs182376587 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHD3 | GRCh38.p7 | 17:7889472 | TCTGACCCCTGACCT[C/T]CCATTCAGAACCAGA | 1107 |
rs182677207 | snp | A/C/G/T | 0.00636936 | 0.0560724 | intron-variant | CHD3 | GRCh38.p7 | 17:7896023 | CTGAGGTCAGGAGAT[A/C/G/T]GAGACTATCCTGGCT | 1107 |
rs182797287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7902008 | CTACTCACCAGAAAA[C/T]TGCACATACAATGAC | 1107 |
rs182931416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7903566 | AGGAGTACTTATCAG[C/T]CCCCTGGGGAGAGAA | 1107 |
rs183053403 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7912968 | AGCAGCAGATACCTA[C/T]GTAGCCTCAGGTTGA | 1107 |
rs183197971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7909830 | CGACCTTTCCTCCTA[C/T]CCCCTCTCACCTTGC | 1107 |
rs183368220 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CHD3 | GRCh38.p7 | 17:7891139 | ACCCCTTGGAATCTG[A/T]TGAAAGCTATGAAAC | 1107 |
rs183454935 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7882935 | GATTCCACAGGCATG[C/G]AATGGGAAGCAAGGG | 1107 |
rs183504471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885624 | GGGTTGGACCGAGGG[A/G]GAGTGGGGTTTCCCC | 1107 |
rs183627742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891268 | TCTTCACTGAGGGGC[A/G]AGGGGTGGAGGGGCC | 1107 |
rs183754558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7894757 | TAATGTATTCCTTTC[G/T]CCCACAATCAACATT | 1107 |
rs184223900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890747 | GGGGCAAAAGGTGAG[C/T]AGAATTAGGGAATGA | 1107 |
rs184250520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7896677 | CCCAAAGTGCTGGGA[C/T]GCGCCTGTTATTCTC | 1107 |
rs184277240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7900141 | GTAGTCTGGGAGGAC[A/G]TCCAGGTTGGAAGAG | 1107 |
rs184405038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904987 | CCCAGAAGGACCAAG[A/G]CCAGAATAAAGGTAG | 1107 |
rs184508659 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905351 | CGGTGTGTGTGACCA[C/T]ATAGGCTAGATCCAG | 1107 |
rs184577010 | snp | C/T | 6.63163e-05 | 0.00575793 | intron-variant | CHD3 | GRCh38.p7 | 17:7897074 | TCCCTTTTTTCTGTG[C/T]CCTGCTAGCTGGAAA | 1107 |
rs185029531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892144 | TAACTGGTGACTGTC[A/T]TTAGTAACGTTGTCT | 1107 |
rs185072164 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883717 | TTAAATGCGTTGTGA[C/T]TTCAATGAGGTATGT | 1107 |
rs185114314 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904735 | TCAGAGCCTTCCTCT[A/C/G]CTAAAAGGGAAAGAC | 1107 |
rs185135326 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | CHD3 | GRCh38.p7 | 17:7889927 | CACTTCCCTGCCACT[G/T]TTGGCCTGTATCTCA | 1107 |
rs185678916 | snp | A/G | 0.000636485 | 0.017828 | intron-variant | CHD3 | GRCh38.p7 | 17:7893573 | AAGAGGGCAAAGGTA[A/G]GGAACTCTCTTCCAA | 1107 |
rs185748492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7907573 | GAGGGTAACATCCTC[A/C]CTTCCTATCCCCTAC | 1107 |
rs185847710 | snp | A/T | 0.000148845 | 0.00862557 | intron-variant | CHD3 | GRCh38.p7 | 17:7900459 | TGAGAGGTGGAGCAG[A/T]TAAAATGAGCTGGTA | 1107 |
rs185861181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7891450 | AACTTCCTTAGCTCA[C/T]TTAGCAGGTCCTGTG | 1107 |
rs186219028 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901450 | GACTTTAATTTCTTA[A/C/T]GGTCTTCCTGTGGCT | 1107 |
rs186368632 | snp | C/T | 0.00104477 | 0.0228318 | intron-variant | CHD3 | GRCh38.p7 | 17:7906820 | ACTGGAGCTTCCTGT[C/T]TGTAAGCGCCTGGAG | 1107 |
rs186552300 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | CHD3 | GRCh38.p7 | 17:7910695 | TGGAAAAACAACTTG[C/G]TAGAACACAGTCATC | 1107 |
rs186664772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888876 | GAAGGGTGAGATCGG[A/G]AAACAAAGGGTATGG | 1107 |
rs186791982 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888280 | AGGTGGCACTGAAGG[A/G]AGGCGAGGCAGCGAC | 1107 |
rs186988843 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHD3 | GRCh38.p7 | 17:7896088 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCACC | 1107 |
rs187075787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7891198 | ACACCAAATTCTACA[C/T]GTCATTTCAGGGAAC | 1107 |
rs187140129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7902048 | TACGGATTTTCAGGG[G/T]GTTCCTGGATTTCCC | 1107 |
rs187208318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7894826 | TCTTCTCTGCACTTC[C/T]AGGATTCAGGTGTCC | 1107 |
rs187467817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7904046 | CATCTCCAAAAGGCA[A/G]TATCCTTTACTCAGC | 1107 |
rs187617703 | snp | C/T | 0.000224861 | 0.0106009 | intron-variant | CHD3 | GRCh38.p7 | 17:7894370 | CTCTCTCTCTCCATC[C/T]CCCCCTGCCCTGCTT | 1107 |
rs187809397 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904910 | ACTGAAGGTGGGCGG[C/T]GAATGGAGATGGTGT | 1107 |
rs187958191 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912024 | GAAGAGAGCTTTGAA[A/G]AGAGGAGGGGGACTT | 1107 |
rs187985833 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7891358 | ATATAGTGAGCCCTC[A/C]CCTGCCCCAACAGCT | 1107 |
rs188208381 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913040 | AGGAGCGCCTATCAA[C/G]ATTCAAAACTGCCTT | 1107 |
rs188509520 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883229 | ACGCCTGGGTATAAC[C/T]CCTACCTCTGCTTTT | 1107 |
rs188617531 | snp | G/T | 0.000724972 | 0.0190253 | intron-variant | CHD3 | GRCh38.p7 | 17:7900274 | TTTTCCTGCCTTGCC[G/T]TGCCCCATCTTTTAG | 1107 |
rs188698521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7892153 | ACTGTCATTAGTAAC[A/G]TTGTCTCACCTACCT | 1107 |
rs188762501 | snp | C/T | 0.00173399 | 0.0293936 | intron-variant | CHD3 | GRCh38.p7 | 17:7890760 | AGTAGAATTAGGGAA[C/T]GAGAGTGAGAAATCT | 1107 |
rs189110559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7897008 | CCCATTCCTCCTGCC[A/G]GCCTCTTCCCGGTTC | 1107 |
rs189253864 | snp | C/G | 1.65384e-05 | 0.00287557 | intron-variant | CHD3 | GRCh38.p7 | 17:7907281 | TCCCCTGTGGAGCGG[C/G]AGGGGAGGGGGCTTG | 1107 |
rs189332258 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905584 | GAGGCTTAGAGGAGG[C/T]GGTGGCTCAGCTAAC | 1107 |
rs189405134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, missense | CHD3, NAA38 | GRCh38.p7 | 17:7887064 | ACCCAGATACACCCC[C/T]TCAGATGACTTTCGG | 1107 |
rs189487777 | snp | G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884311 | GTGGCGGTGCTGGAG[G/T]GGGGGTTGTTTTAAA | 1107 |
rs189937475 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904990 | AGAAGGACCAAGGCC[A/G]GAATAAAGGTAGACA | 1107 |
rs190035867 | snp | C/T | 1.8267e-05 | 0.00302211 | intron-variant | CHD3 | GRCh38.p7 | 17:7893578 | GGCAAAGGTAGGGAA[C/T]TCTCTTCCAACAACT | 1107 |
rs190140455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7894840 | CTAGGATTCAGGTGT[A/C]CTGTCTTTGCCTGTA | 1107 |
rs190176614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889428 | TTAGTAGGAGGGGAG[A/G]GAGGGGAGTGGTTTG | 1107 |
rs190287556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891465 | CTTAGCAGGTCCTGT[A/G]CCCCTTCCTTAGGCC | 1107 |
rs190389808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888364 | TGGCTGTTGAGGGAA[A/G]GAGAAAGGATTGTGT | 1107 |
rs190684197 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHD3 | GRCh38.p7 | 17:7901573 | TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG | 1107 |
rs190903037 | snp | C/G | 1.66852e-05 | 0.0028883 | intron-variant | CHD3 | GRCh38.p7 | 17:7910807 | CTTTCCTCTCACAGA[C/G]TATGAACTAACTCCA | 1107 |
rs191034513 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7902258 | GAAACCCTGTCTCTA[C/G]TTAAAATACAAAAAT | 1107 |
rs191081704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890169 | GTTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 1107 |
rs191243328 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7891364 | TGAGCCCTCCCCTGC[C/T]CCAACAGCTCCATCT | 1107 |
rs191420949 | snp | A/C | 0.304688 | 0.243945 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885109 | GCCCCGACTCCCCCC[A/C]CAAGCCCGAGTGGGA | 1107 |
rs191465469 | snp | A/C/G | 0.00205816 | 0.0320147 | intron-variant | CHD3 | GRCh38.p7 | 17:7908854 | AGGGAGGAAAGGAGC[A/C/G]GGTTATAGACGGGCT | 1107 |
rs191560114 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7891199 | CACCAAATTCTACAC[A/G]TCATTTCAGGGAACT | 1107 |
rs191852106 | snp | C/T | 3.41717e-05 | 0.00413336 | intron-variant | CHD3 | GRCh38.p7 | 17:7894400 | TCCTTATCCCTCCAC[C/T]GGGGTATATGACAGT | 1107 |
rs192301551 | snp | A/C/G | 0.00108373 | 0.0232531 | intron-variant | CHD3 | GRCh38.p7 | 17:7901407 | GCTGTCTTTACATCT[A/C/G]CTTCCTCTTCCCTCT | 1107 |
rs192432724 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912588 | CCTCCCAGGAGGGGC[C/T]GGGGAGAGTGGCAGT | 1107 |
rs192435878 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7882900 | CACTGGAGAGGTAGA[A/G]GAATAACCCAGAGAG | 1107 |
rs192531054 | snp | C/G/T | 0.00332274 | 0.0406253 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905065 | GCATATCCCGAGAGC[C/G/T]CTCCCTGACCACTGG | 1107 |
rs192700597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904647 | CCAGATGCAGGCAGT[A/T]AAGGGGGGAAGTGAT | 1107 |
rs192767079 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CHD3 | GRCh38.p7 | 17:7896315 | CCACCCAGGCCTTGT[C/T]TTCTGAAACTGTTGC | 1107 |
rs192885762 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883389 | CAGATTTGACTCTTT[C/G]CTCTTTATCCTAAAA | 1107 |
rs193011709 | snp | A/G | 6.89144e-05 | 0.00586962 | intron-variant | CHD3 | GRCh38.p7 | 17:7897039 | CTTGTTGTCCTCTGT[A/G]AGTGTCAGGACTATC | 1107 |
rs193183095 | snp | A/G | 2.16997e-05 | 0.00329384 | intron-variant | CHD3 | GRCh38.p7 | 17:7890778 | GAGTGAGAAATCTGC[A/G]TTAAAGACGGGCATG | 1107 |
rs199520081 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | CHD3 | GRCh38.p7 | 17:7908649 | AGTGTTCAAAGCCAA[A/G]CCCATTCCTGTTAAA | 1107 |
rs199568516 | snp | A/G | 3.33745e-05 | 0.00408487 | intron-variant | CHD3 | GRCh38.p7 | 17:7894101 | CTCACTGACGGCCAC[A/G]GGGCTATGGGCAGTA | 1107 |
rs199623374 | snp | C/T | 0.000201633 | 0.0100387 | intron-variant | CHD3 | GRCh38.p7 | 17:7901024 | AGGGAGCTGATCGAA[C/T]GCCCATTCTCAGAAA | 1107 |
rs199623433 | snp | C/T | 0.000462466 | 0.0151993 | intron-variant | CHD3 | GRCh38.p7 | 17:7910422 | TCTCTGTGGCCCGGG[C/T]CCCAGTTCTGAACCA | 1107 |
rs199639442 | snp | C/G | 0.000115406 | 0.00759537 | intron-variant | CHD3 | GRCh38.p7 | 17:7911427 | ACGTTTGAGAGTGAT[C/G]TGGAGATTGATCTTT | 1107 |
rs199688958 | snp | C/T | 0.000539162 | 0.0164101 | intron-variant | CHD3 | GRCh38.p7 | 17:7890786 | AATCTGCATTAAAGA[C/T]GGGCATGAGGAGGGG | 1107 |
rs199752977 | snp | G/T | 0.00299544 | 0.0385843 | intron-variant | CHD3 | GRCh38.p7 | 17:7902858 | GGGGGCATGGTTGTT[G/T]GTCATCAGAGAACAT | 1107 |
rs199768991 | snp | C/G/T | 3.29702e-05 | 0.00406008 | missense | CHD3 | GRCh38.p7 | 17:7907168 | AAGGCATAAGGACAC[C/G/T]TCTTGAGAAGGAGGA | 1107 |
rs199825581 | snp | A/G | 3.36276e-05 | 0.00410032 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910914 | GCGCCGCACCCGTAG[A/G]GGCCCTGGCCGCCGC | 1107 |
rs199832347 | in-del | -/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896409 | TTCTTTTTTTTTCTA[-/T]TTTTTTTTTTTTTTA | 1107 |
rs199833542 | snp | C/T | | | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7895391 | ATTGGCGGTGGGGGG[C/T]GCCACCTGTAGCAGT | 1107 |
rs199851449 | snp | G/T | 0.000198085 | 0.00995004 | missense | CHD3 | GRCh38.p7 | 17:7899047 | CAGCCACGGTTTATC[G/T]CAGCCACTGGAGGCA | 1107 |
rs199858009 | snp | C/T | 5.31995e-05 | 0.00515722 | utr-variant-3-prime, stop-gained | CHD3 | GRCh38.p7 | 17:7911624 | CCCAGGCCCCGTCCC[C/T]GAGGCCGACCCCCAG | 1107 |
rs199898244 | snp | C/G/T | 0.00648945 | 0.0565935 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893487 | CCCCATAGCACCCTC[C/G/T]GGACCCCCCGCCCTT | 1107 |
rs199898991 | snp | A/G | 9.90442e-05 | 0.0070365 | missense | CHD3 | GRCh38.p7 | 17:7894200 | ACAGTGCCTCAGGCC[A/G]GCCTGATGGCCCTGT | 1107 |
rs199912893 | snp | C/G | 0.000221072 | 0.0105113 | intron-variant | CHD3 | GRCh38.p7 | 17:7910996 | GGTGTTTTCCTACCC[C/G]CTGCTACTCACACTC | 1107 |
rs199967836 | snp | C/G/T | 1.64917e-05 | 0.00287151 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903337 | CCGGTTTGTGACTCG[C/G/T]GCGTCAGTGGAAGAG | 1107 |
rs200004902 | snp | C/T | 0.00061621 | 0.0175421 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910572 | TGGCCAGCAAGGGCA[C/T]GGAGCCTCACCCCAC | 1107 |
rs200031730 | snp | A/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7891610 | TCATGCCTGTAATCC[A/C]AGCACTTTGGGAGGC | 1107 |
rs200096964 | snp | A/G | 5.17264e-05 | 0.00508532 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907652 | AGCCGTTGGATGGAC[A/G]GGAACACAGGGAGAG | 1107 |
rs200126449 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7895054 | CGGCGGGGAGCTCCT[A/G]TGCTGTGACGCGTGC | 1107 |
rs200160738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | CHD3 | GRCh38.p7 | 17:7909379 | GGGGAGGGCCCACAA[C/T]GCTGCGTAAGTCTTC | 1107 |
rs200224257 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883833 | TTCAAAAAAAAAAAA[-/A]GCTTTTCTTTAGAGA | 1107 |
rs200279688 | snp | C/G | 0.000233497 | 0.0108025 | intron-variant | CHD3 | GRCh38.p7 | 17:7895302 | GGGTTCTTTCTGCCT[C/G]TTTCTTTCCTCCTCC | 1107 |
rs200287864 | snp | C/T | 0.00146832 | 0.0270556 | intron-variant | CHD3 | GRCh38.p7 | 17:7899340 | CCCATTCTTGACTCC[C/T]AGGGCCACACAAAAG | 1107 |
rs200329628 | snp | C/T | 0.00057354 | 0.0169246 | intron-variant | CHD3 | GRCh38.p7 | 17:7904036 | TATCCCAGGCCATCT[C/T]CAAAAGGCAGTATCC | 1107 |
rs200425322 | snp | A/G | 1.79615e-05 | 0.00299674 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908433 | GCAGAATGAGGAACG[A/G]GCAGCTATTTCCTCG | 1107 |
rs200434912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, missense | CHD3 | GRCh38.p7 | 17:7907891 | ACCTGTCTGTCCTAG[C/T]AGAAGATGTAAAAGG | 1107 |
rs200461939 | snp | C/G/T | 0.000131779 | 0.00811626 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7895448 | ATCCAGATGTCCCAC[C/G/T]CCCCCGTCCTCTTCA | 1107 |
rs200472460 | snp | C/T | 0.000103937 | 0.00720819 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906709 | GAAGGTATCAGTCTT[C/T]CTGTCACCCAAAGAA | 1107 |
rs200501981 | snp | A/C | 5.01517e-05 | 0.00500733 | intron-variant | CHD3 | GRCh38.p7 | 17:7895292 | ATCTAACAATGGGTT[A/C]TTTCTGCCTCTTTCT | 1107 |
rs200504536 | snp | A/G | 0.000282287 | 0.011877 | intron-variant | CHD3 | GRCh38.p7 | 17:7893764 | TTCCAGGATGTCATG[A/G]CCTCTCCTTTTTCCT | 1107 |
rs200555446 | snp | C/G | 1.64811e-05 | 0.00287059 | missense | CHD3 | GRCh38.p7 | 17:7908770 | GAGCCATTTAAAACT[C/G]AAGCCAATAAGGGGA | 1107 |
rs200571808 | snp | C/T | 3.31625e-05 | 0.00407188 | intron-variant | CHD3 | GRCh38.p7 | 17:7900524 | GGGCAAGGAACTTGC[C/T]GACCTGTTAATTTTC | 1107 |
rs200597692 | snp | A/C/T | 0.00883584 | 0.0658784 | intron-variant | CHD3 | GRCh38.p7 | 17:7910828 | ACTAACTCCAACTTC[A/C/T]GCTTCCTCTCTGTTC | 1107 |
rs200617599 | in-del | -/A | | | intron-variant | CHD3 | GRCh38.p7 | 17:7902420 | ATGAGACTCCATCTC[-/A]AAAAAAAAATAAAAA | 1107 |
rs200694419 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7902898 | GGTGGACAGAACTAC[C/G/T]GGGTACAAGAAAAAC | 1107 |
rs200709315 | in-del | -/TC | | | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7912878 | TTTTCCTCATTTTTA[-/TC]TCTTAGATTATTCAC | 1107 |
rs200737527 | snp | A/G | 0.00019989 | 0.00999525 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910573 | GGCCAGCAAGGGCAC[A/G]GAGCCTCACCCCACA | 1107 |
rs200795614 | snp | A/G | 0.00019883 | 0.00996873 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905996 | GGAGTTTAAGTGAGT[A/G]TGGGTGATACAGGGC | 1107 |
rs200817173 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7912950 | CTGTAGAGAAGGAGG[A/G]TGAGCAGCAGATACC | 1107 |
rs200846584 | snp | A/C | 0.000798403 | 0.0199641 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893475 | CTCGTCGGCCACCCC[A/C]ATAGCACCCTCCGGA | 1107 |
rs200857173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7893962 | GTCCCTGTCTACTAA[A/G]CACCTGGGGGCCAAG | 1107 |
rs200904309 | snp | C/T | 4.95013e-05 | 0.00497475 | synonymous-codon, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906601 | TGAGCCTGGGGCAGA[C/T]GGCTCTGAAACCTTT | 1107 |
rs200905681 | snp | C/T | 1.67234e-05 | 0.00289161 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903266 | CACTTTCTCTTGCCC[C/T]TGCAGGCCTTTAGCC | 1107 |
rs200956669 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7903895 | TCGGCTGTTGGACCG[A/G]AACCAGGATGCAACT | 1107 |
rs200997129 | snp | C/T | 5.07894e-05 | 0.00503906 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910966 | GCCTGCAGGGTCCTT[C/T]ATCACAGGTCAGCTG | 1107 |
rs201016344 | snp | G/T | 0.00199792 | 0.0315431 | missense | CHD3 | GRCh38.p7 | 17:7895006 | GAAGGAGGAGGAGGA[G/T]GATCACATGGAGTAC | 1107 |
rs201018055 | snp | C/T | 1.65847e-05 | 0.0028796 | intron-variant | CHD3 | GRCh38.p7 | 17:7895555 | CAGGTACTAGGACCT[C/T]TTCTTTCCCTCTCCC | 1107 |
rs201043938 | snp | A/G | 4.98691e-05 | 0.0049932 | intron-variant | CHD3 | GRCh38.p7 | 17:7893755 | CCTCCATAATTCCAG[A/G]ATGTCATGACCTCTC | 1107 |
rs201044551 | snp | A/G | 4.94572e-05 | 0.00497254 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897259 | TTTTGGCATCAAGCC[A/G]GAGTGGATGACCGTC | 1107 |
rs201048464 | snp | G/T | 0.000724602 | 0.0190204 | missense | CHD3 | GRCh38.p7 | 17:7893872 | GAAGCTTCGGGGAAA[G/T]AAAATGGCACCACTC | 1107 |
rs201161801 | snp | C/T | 0.000153018 | 0.00874561 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907640 | GGGGGGAGGAGAAGC[C/T]GTTGGATGGACAGGA | 1107 |
rs201169642 | snp | C/G/T | 0.000149374 | 0.00864087 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910857 | TCCAGGCCTACCCGC[C/G/T]GGGTCCCTACGCTAC | 1107 |
rs201176893 | snp | A/C | 0.00167013 | 0.0288492 | utr-variant-3-prime, missense | CHD3 | GRCh38.p7 | 17:7911616 | GCCCTTCACCCAGGC[A/C]CCGTCCCCGAGGCCG | 1107 |
rs201193191 | snp | A/C | 1.66582e-05 | 0.00288597 | intron-variant | CHD3 | GRCh38.p7 | 17:7908535 | GATACACATGCAAGA[A/C]GGAAAAGGTTCTCTC | 1107 |
rs201212602 | snp | C/T | 1.65247e-05 | 0.00287438 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910471 | CGACATGAAGGCGGA[C/T]GTGACCCGCCTGCCA | 1107 |
rs201232886 | snp | A/C | 0.0019981 | 0.0315446 | intron-variant | CHD3 | GRCh38.p7 | 17:7893979 | ACCTGGGGGCCAAGG[A/C]TCCAGAGACAGGGAT | 1107 |
rs201268003 | in-del | -/A | | | intron-variant | CHD3 | GRCh38.p7 | 17:7891875 | TCAAAAAAAAAAAAA[-/A]GAAAAAATAGTGCCG | 1107 |
rs201302235 | snp | G/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7901944 | CATCTTATTGGCAGG[G/T]GAGGGTGAAGGGCAC | 1107 |
rs201309725 | snp | A/G | 0.000137722 | 0.00829711 | missense | CHD3 | GRCh38.p7 | 17:7908459 | CCTCGGGGAAACTCA[A/G]TGAGATCTGGCACAG | 1107 |
rs201318714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905209 | ACCTCTTCCCGTTTT[A/T]TTTTCCAGTTTGCTT | 1107 |
rs201334286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7907089 | AGGAGTCAGGGCGGG[A/G]GAATCTCTGTCTTTA | 1107 |
rs201425133 | snp | C/T | 0.000494128 | 0.0157105 | intron-variant | CHD3 | GRCh38.p7 | 17:7908688 | TGGTTCCTTTTCCTT[C/T]ATTGGTAGCCATGGC | 1107 |
rs201436753 | snp | C/G | 0.00199793 | 0.0315432 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910882 | CGCTACACCTCCGGG[C/G]TACGGGGCGGCCTTC | 1107 |
rs201488618 | snp | C/G/T | 0.00185766 | 0.0304204 | intron-variant | CHD3 | GRCh38.p7 | 17:7907343 | TCCTGACCCCATTGT[C/G/T]CTCTTCCAGGCTGAT | 1107 |
rs201498151 | snp | A/G/T | 0.000321195 | 0.0126688 | missense | CHD3 | GRCh38.p7 | 17:7910916 | GCCGCACCCGTAGGG[A/G/T]CCCTGGCCGCCGCAG | 1107 |
rs201554552 | snp | C/T | 0.000313033 | 0.0125067 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7902675 | CAAGTATGAGCGCAT[C/T]GATGGTGGTATCACG | 1107 |
rs201582788 | snp | A/G | 0.00458459 | 0.0476579 | intron-variant | CHD3 | GRCh38.p7 | 17:7907740 | CACCTGGGTCCCAGA[A/G]GGCATCAGGGGAGGT | 1107 |
rs201611412 | snp | C/T | 0.000115368 | 0.00759412 | missense | CHD3 | GRCh38.p7 | 17:7911478 | GCCGCCACCAACGGC[C/T]CTCCAGTGCTTGTGA | 1107 |
rs201620031 | snp | A/G | 8.31525e-05 | 0.00644743 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906024 | GGCTGAGTTGGACGC[A/G]AGGGGAAGAGCTTTG | 1107 |
rs201632697 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | CHD3 | GRCh38.p7 | 17:7890268 | AACTCCGTCTCTACT[-/A]AAAAATACAAAAATC | 1107 |
rs201727011 | snp | G/T | 0.0423737 | 0.139253 | missense, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905953 | CCACACAGTGGCTGG[G/T]GCGGGACCTGAGGGG | 1107 |
rs201739166 | snp | A/C/G | 0.000263537 | 0.0114762 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7895451 | CAGATGTCCCACCCC[A/C/G]CCGTCCTCTTCAAGG | 1107 |
rs201772788 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885091 | GCCGCCAGGTAAGCG[C/G]CCGCCCCGACTCCCC | 1107 |
rs201793105 | snp | C/T | 0.00036348 | 0.0134762 | intron-variant | CHD3 | GRCh38.p7 | 17:7893790 | TTCCTCTTCTCACCC[C/T]GACTCCTCATTCAGG | 1107 |
rs201820288 | snp | A/C | 0.00182892 | 0.0301847 | intron-variant | CHD3 | GRCh38.p7 | 17:7890934 | ACCAAAGCCCCTCTC[A/C]CGCAGCAAGTGGAAC | 1107 |
rs201826381 | snp | A/G/T | 6.80566e-05 | 0.00583304 | intron-variant | CHD3 | GRCh38.p7 | 17:7894404 | TATCCCTCCACCGGG[A/G/T]TATATGACAGTCCTG | 1107 |
rs201848582 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7895135 | CAATGGTGAATGGCT[A/G]TGTCCCCGATGCACA | 1107 |
rs201865565 | in-del | -/T | 0.497959 | 0.0318836 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913169 | GAAGCAAAGGCACAC[-/T]TTTTTTTTTTTTTTT | 1107 |
rs201923001 | snp | C/T | 1.66502e-05 | 0.00288527 | intron-variant | CHD3 | GRCh38.p7 | 17:7910821 | ACTATGAACTAACTC[C/T]AACTTCTGCTTCCTC | 1107 |
rs201932618 | snp | C/T | 0.000197694 | 0.00994021 | missense | CHD3 | GRCh38.p7 | 17:7893852 | CGAGTGCCTGATGGA[C/T]GCAAGAAGCTTCGGG | 1107 |
rs201974846 | snp | A/G | 3.30453e-05 | 0.00406467 | intron-variant | CHD3 | GRCh38.p7 | 17:7910421 | TTCTCTGTGGCCCGG[A/G]CCCCAGTTCTGAACC | 1107 |
rs202009423 | snp | C/T | 0.000568125 | 0.0168446 | intron-variant | CHD3 | GRCh38.p7 | 17:7894097 | CTGCCTCACTGACGG[C/T]CACGGGGCTATGGGC | 1107 |
rs202017045 | snp | A/G | 0.000141505 | 0.00841027 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904638 | AGGACTGCCCCAGAT[A/G]CAGGCAGTAAAGGGG | 1107 |
rs202059923 | snp | A/G | 0.000576896 | 0.016974 | missense | CHD3 | GRCh38.p7 | 17:7906929 | CTGATGCCTGACCCC[A/G]GCGCCGATTCTAAGC | 1107 |
rs202073230 | snp | A/C/G | 0.000153186 | 0.00875041 | intron-variant | CHD3 | GRCh38.p7 | 17:7907722 | TGGGTGGAAGGGACC[A/C/G]GACACCTGGGTCCCA | 1107 |
rs202126136 | snp | A/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7892489 | ATTTCGCTGTTTTTT[A/T]TTTCCCCTTTTTTTT | 1107 |
rs202153613 | in-del | -/CTA | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896406 | TTTTTCTTTTTTTTT[-/CTA]TTTTTTTTTTTTTTT | 1107 |
rs202211353 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884157 | TTATGAAAAAGGAGA[-/A]ATTTGTGGGTTTCTG | 1107 |
rs202235515 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905051 | GGGCCTCAGCATGGG[C/T]ATATCCCGAGAGCCC | 1107 |
rs267605095 | snp | C/T | 4.95201e-05 | 0.0049757 | CHD3 | 17 | allele_origin=T(somatic)/C(germline) | 17:7895344 | CATCCCAAAGTGCCC[C/T]GTGCTGAAGGGTCGA | 1107 |
rs367543897 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893286 | CTTCTATATTTACAG[A/G]CCCCTAATTGCTAAG | 1107 |
rs367548976 | snp | C/T | 0.000217743 | 0.0104319 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910900 | CGGGGCGGCCTTCAG[C/T]GCCGCACCCGTAGGG | 1107 |
rs367555302 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7900306 | TTTTCAGGGTTCTCA[A/G]TGGTTACAAGATAGA | 1107 |
rs367578967 | snp | G/T | 3.48602e-05 | 0.00417479 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905724 | GAGAGCTGGGCCCAG[G/T]GTTCCTGAGTTCTCC | 1107 |
rs367610195 | snp | C/T | 0.000200038 | 0.00999895 | intron-variant, nc-transcript-variant | CHD3, SCARNA21 | GRCh38.p7 | 17:7906216 | TCCCCAGGGGAGGGG[C/T]GTTGAAGCAAGGAGC | 1107 |
rs367681308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7892622 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC | 1107 |
rs367753545 | snp | A/G | 7.33568e-05 | 0.00605583 | utr-variant-3-prime, missense | CHD3 | GRCh38.p7 | 17:7911631 | CCCGTCCCCGAGGCC[A/G]ACCCCCAGCTCAAGC | 1107 |
rs367915692 | snp | C/T | 0.00050819 | 0.0159323 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906104 | TGATTATCACCCTCC[C/T]TGTCATACAATACTT | 1107 |
rs367926390 | snp | C/T | 0.000119961 | 0.00774377 | intron-variant | CHD3 | GRCh38.p7 | 17:7895202 | GGCCTGATCCCTTCC[C/T]CCATCCCTGGGGCCC | 1107 |
rs367944735 | snp | A/G | 0.000219142 | 0.0104653 | intron-variant | CHD3 | GRCh38.p7 | 17:7893577 | GGGCAAAGGTAGGGA[A/G]CTCTCTTCCAACAAC | 1107 |
rs367949775 | snp | C/T | 0.000500375 | 0.0158094 | intron-variant, synonymous-codon | CHD3 | GRCh38.p7 | 17:7909352 | GGGTAAGGGCCGCGG[C/T]GGCCCCGCGCGGGGG | 1107 |
rs367980238 | snp | C/G/T | 1.65151e-05 | 0.00287355 | intron-variant | CHD3 | GRCh38.p7 | 17:7900247 | GTCGGTCACTTGTCA[C/G/T]TAATAAGCCCATTTT | 1107 |
rs367982642 | snp | C/T | 3.38834e-05 | 0.00411589 | intron-variant | CHD3 | GRCh38.p7 | 17:7907321 | TACCTGGGAGCCCTC[C/T]GGCTCATCCTGACCC | 1107 |
rs368018825 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7901232 | TCCTCCTCCTCTCTC[C/T]TCCCTTTTCAGGAGT | 1107 |
rs368066795 | snp | A/G | 3.49406e-05 | 0.0041796 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908448 | GGCAGCTATTTCCTC[A/G]GGGAAACTCAATGAG | 1107 |
rs368092902 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7892753 | TCCCACCTTGGCCTC[C/T]CAAAGTACTGGGATT | 1107 |
rs368101383 | snp | C/T | 3.30011e-05 | 0.00406195 | missense | CHD3 | GRCh38.p7 | 17:7898530 | GACCCTGCCCAGCCC[C/T]GCAAGTATAAGAAGA | 1107 |
rs368103933 | snp | C/T | 0.000164823 | 0.00907659 | missense | CHD3 | GRCh38.p7 | 17:7906909 | GGCGTTGGTCAATGC[C/T]GGAACTGATGCCTGA | 1107 |
rs368108786 | snp | G/T | 1.72335e-05 | 0.00293538 | intron-variant | CHD3 | GRCh38.p7 | 17:7901378 | CATCTTCTCGCAGGT[G/T]ACCTGTGCCCTTAGC | 1107 |
rs368128246 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7911753 | TCAAGAAGGGCCCTT[C/T]GTCTTTCTCCACTCC | 1107 |
rs368192625 | snp | C/G | 0.000341605 | 0.0130647 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907627 | ACGCCAGGAGAAAGG[C/G]GGGAGGAGAAGCCGT | 1107 |
rs368221837 | snp | A/C/G | 0.000115452 | 0.00759698 | intron-variant | CHD3 | GRCh38.p7 | 17:7906865 | TCCCACCCTGCCACC[A/C/G]CAGGTGCAGGAGTTT | 1107 |
rs368228432 | snp | A/G | 8.48947e-05 | 0.00651461 | intron-variant | CHD3 | GRCh38.p7 | 17:7903804 | GAACCCAAAGTTCCC[A/G]TTTGTTTTCCCTCTC | 1107 |
rs368467918 | snp | C/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7901641 | TCAGCCTCCCAAGTA[C/G]CTGGGATTACAGGCG | 1107 |
rs368553528 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7891924 | AGAAGGCACTTTAAC[A/G]TATCAGTTCAGTGCT | 1107 |
rs368579336 | snp | C/T | 3.29794e-05 | 0.00406061 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897995 | AAAGGGGAATTACCA[C/T]TATCTAGTAAAATGG | 1107 |
rs368591051 | snp | C/G | 0.000505263 | 0.0158864 | intron-variant | CHD3 | GRCh38.p7 | 17:7907591 | TCCTATCCCCTACCC[C/G]CTCCCACAGCCACAG | 1107 |
rs368619557 | snp | C/T | 4.97352e-05 | 0.00498649 | intron-variant | CHD3 | GRCh38.p7 | 17:7906821 | CTGGAGCTTCCTGTC[C/T]GTAAGCGCCTGGAGC | 1107 |
rs368622201 | snp | C/T | 0.000198843 | 0.00996906 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894129 | GTATGTTTTTCAGAG[C/T]GACGAAGGTCCTGAA | 1107 |
rs368719593 | snp | C/G | 1.64757e-05 | 0.00287012 | missense | CHD3 | GRCh38.p7 | 17:7897208 | GCGTAAAGTGAAAGA[C/G]CCGCACTATGCTGAG | 1107 |
rs368755514 | snp | C/T | 6.59424e-05 | 0.00574168 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905827 | ACCCTAGACATTTGT[C/T]GCCATTGCCTCCTTG | 1107 |
rs368758448 | snp | A/G | 0.000197791 | 0.00994266 | missense | CHD3 | GRCh38.p7 | 17:7911466 | CTTTCCCAAACAGCC[A/G]CCACCAACGGCCCTC | 1107 |
rs368773406 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | CHD3 | GRCh38.p7 | 17:7897187 | GGATGATGGGAAGAG[C/G]GACAAGCGTAAAGTG | 1107 |
rs368825536 | snp | A/C/T | 8.23847e-05 | 0.00641769 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905055 | CTCAGCATGGGCATA[A/C/T]CCCGAGAGCCCTCCC | 1107 |
rs368862267 | snp | A/G | 9.38725e-05 | 0.00685036 | synonymous-codon, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890699 | AAAAAAGGAGAAGAA[A/G]ACAAAGCGGCGGAAA | 1107 |
rs368898360 | snp | C/T | 5.04689e-05 | 0.00502314 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908000 | GTTCATGTTCAATAT[C/T]GCCGATGGTGGCTTC | 1107 |
rs368907014 | snp | C/T | 0.000132018 | 0.00812351 | intron-variant | CHD3 | GRCh38.p7 | 17:7891068 | CCAGTTCATGAGGTG[C/T]GGTAAGACTGGGGAA | 1107 |
rs368914388 | snp | A/G | | | missense | CHD3 | GRCh38.p7 | 17:7898534 | CTGCCCAGCCCCGCA[A/G]GTATAAGAAGAAGAA | 1107 |
rs369019964 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | CHD3 | GRCh38.p7 | 17:7900940 | CTGCTTAATATCATG[A/G]TGGATCTTAAGAAGT | 1107 |
rs369027043 | snp | A/G | 0.000214778 | 0.0103606 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910492 | CCGCCTGCCAGCCAC[A/G]CTGTCCCGAATACCC | 1107 |
rs369109599 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7906864 | CTCCCACCCTGCCAC[C/T]CCAGGTGCAGGAGTT | 1107 |
rs369143986 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7894692 | TTACCCTCTTCCTGC[C/T]CCCAGATGGCTGGAC | 1107 |
rs369145256 | snp | A/G | 0.00206525 | 0.032068 | intron-variant | CHD3 | GRCh38.p7 | 17:7893261 | ATCTGTGAAGGGTCC[A/G]AGTTTTCTGCTTCTA | 1107 |
rs369205747 | snp | A/G | 1.64931e-05 | 0.00287163 | missense | CHD3 | GRCh38.p7 | 17:7893814 | ATTCAGGTCCAGGCC[A/G]TAAGAGGCGGAGTAA | 1107 |
rs369319748 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905232 | GTTTGCTTTAAGCCC[A/G]CTGTTTTTATACAAG | 1107 |
rs369355870 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912241 | GTGTTGGGAATGTTC[C/T]CCCCTCCCTAGGGAC | 1107 |
rs369388251 | snp | A/G | 3.32497e-05 | 0.00407722 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894258 | GCCAGGAAGGAAGAA[A/G]AAGAAGGGTAAGGAG | 1107 |
rs369420111 | snp | A/C/G | 0.000178772 | 0.009453 | synonymous-codon, intron-variant | CHD3 | GRCh38.p7 | 17:7907683 | GCCGGAGGGGGAAAC[A/C/G]GGGGATTTGGGCAAG | 1107 |
rs369429931 | snp | C/G | 0.000102344 | 0.00715272 | intron-variant | CHD3 | GRCh38.p7 | 17:7894903 | TGTCTGTGTGTCTAT[C/G]CTTGGCCCCCTAGGA | 1107 |
rs369474195 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886263 | AGACCGCTGCGCCGC[A/G]TCAGGCGCCCAGCGG | 1107 |
rs369508268 | snp | A/G | 2.92368e-05 | 0.00382329 | intron-variant | CHD3 | GRCh38.p7 | 17:7889797 | TGTCAAGAATTCCTA[A/G]CTCTGTGGCAAGGCT | 1107 |
rs369516160 | snp | C/G | 3.29946e-05 | 0.00406155 | intron-variant | CHD3 | GRCh38.p7 | 17:7907100 | CGGGAGAATCTCTGT[C/G]TTTATCACTGTGCCT | 1107 |
rs369524414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7908642 | AGGAAGAAGTGTTCA[A/G]AGCCAAGCCCATTCC | 1107 |
rs369541480 | snp | A/G | 0.000115585 | 0.00760126 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910468 | GAGCGACATGAAGGC[A/G]GACGTGACCCGCCTG | 1107 |
rs369558887 | snp | C/T | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7907944 | CCTCGAGATGAGCCA[C/T]GGTCCAATGGGCGAC | 1107 |
rs369568031 | in-del | -/G | 0.0182019 | 0.0936463 | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912802 | GAGTTTTTGGGGGGA[-/G]GGATAAGAAAGGTTG | 1107 |
rs369569998 | snp | C/T | 1.70061e-05 | 0.00291595 | intron-variant | CHD3 | GRCh38.p7 | 17:7894307 | CTGTCAGTGGGCCGT[C/T]CTCTCATTCTTATTT | 1107 |
rs369604836 | snp | C/T | 0.000117784 | 0.0076732 | missense | CHD3 | GRCh38.p7 | 17:7910907 | GCCTTCAGCGCCGCA[C/T]CCGTAGGGGCCCTGG | 1107 |
rs369686403 | snp | A/G | 0.000197759 | 0.00994184 | missense | CHD3 | GRCh38.p7 | 17:7899186 | CCATCGTCTTCCTCT[A/G]CTCACTCTACAAGGA | 1107 |
rs369867491 | snp | G/T | 0.000671913 | 0.0183168 | intron-variant | CHD3 | GRCh38.p7 | 17:7898635 | TTGTTTCTGGAGTGA[G/T]GGTGATCGAAGATTT | 1107 |
rs369890808 | snp | C/T | 3.29881e-05 | 0.00406115 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7906946 | CGCCGATTCTAAGCG[C/T]TCCTCCAGAGCCTCC | 1107 |
rs370001984 | snp | A/C | 1.64999e-05 | 0.00287222 | intron-variant | CHD3 | GRCh38.p7 | 17:7900741 | GCAGAAGTAAGATGC[A/C]AGACGAGCTGCCTGG | 1107 |
rs370029917 | snp | C/T | 0.000181865 | 0.00953411 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906508 | CACTGCCCTATACCC[C/T]TTCTGTGGCTCCCCT | 1107 |
rs370043411 | snp | C/T | 1.66515e-05 | 0.00288539 | intron-variant | CHD3 | GRCh38.p7 | 17:7897964 | CCCATGGCCTCCTGC[C/T]CCACAGTGTGGATAA | 1107 |
rs370057292 | snp | C/G | 8.24069e-05 | 0.00641846 | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888987 | AGGTAATTGTGGAGA[C/G]TTTCTCCTGTGTGAT | 1107 |
rs370123471 | snp | C/T | 0.000167912 | 0.00916121 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903248 | CTCCCCTGACCCACC[C/T]GCCACTTTCTCTTGC | 1107 |
rs370127612 | snp | C/G | 3.4002e-05 | 0.00412309 | intron-variant | CHD3 | GRCh38.p7 | 17:7910994 | CTGGTGTTTTCCTAC[C/G]CCCTGCTACTCACAC | 1107 |
rs370143174 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905067 | ATATCCCGAGAGCCC[C/T]CCCTGACCACTGGGC | 1107 |
rs370157863 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7898785 | GCCACTAGAGATAGC[C/T]CACTGGTGGCTCTGT | 1107 |
rs370162536 | snp | C/G | 1.70009e-05 | 0.0029155 | intron-variant, splice-acceptor-variant | CHD3 | GRCh38.p7 | 17:7907890 | GACCTGTCTGTCCTA[C/G]CAGAAGATGTAAAAG | 1107 |
rs370171222 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897292 | CCGCATCATCAACCA[C/T]AGGTGAATCCTCGGT | 1107 |
rs370187934 | snp | A/C | 9.91424e-05 | 0.00703998 | intron-variant | CHD3 | GRCh38.p7 | 17:7893789 | TTTCCTCTTCTCACC[A/C]CGACTCCTCATTCAG | 1107 |
rs370277310 | snp | A/C | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884071 | CCTTCATGCCCCCCC[A/C]ACACACACACACACA | 1107 |
rs370465148 | snp | C/T | 1.66535e-05 | 0.00288556 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910885 | TACACCTCCGGGGTA[C/T]GGGGCGGCCTTCAGC | 1107 |
rs370479830 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7894965 | GAAGAAGAAGAATAC[A/G]AAGAGGAGGGAGAGG | 1107 |
rs370513167 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7896356 | TTTTATTTATTCTCC[A/G/T]TCTTGGCTTTGACTC | 1107 |
rs370525301 | snp | C/T | 4.94743e-05 | 0.0049734 | intron-variant | CHD3 | GRCh38.p7 | 17:7890935 | CCAAAGCCCCTCTCC[C/T]GCAGCAAGTGGAACA | 1107 |
rs370538446 | snp | A/G | 5.06864e-05 | 0.00503395 | intron-variant | CHD3 | GRCh38.p7 | 17:7899570 | TACCTCATATCCTCT[A/G]AGACCCTCAAAGCTG | 1107 |
rs370835305 | snp | A/G | 3.32867e-05 | 0.00407949 | intron-variant | CHD3 | GRCh38.p7 | 17:7897329 | GAAGTCAGACCTGGT[A/G]TATGACATTATTCTT | 1107 |
rs370869999 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894551 | TGCCTACCACCTCGT[C/T]TGCCTTGATCCTGAG | 1107 |
rs370878378 | snp | C/G/T | 0.000220416 | 0.010496 | intron-variant | CHD3 | GRCh38.p7 | 17:7910599 | CCACACCGGTAACCC[C/G/T]CTTTCCCCCTAGCTC | 1107 |
rs370878395 | snp | C/T | 1.65924e-05 | 0.00288027 | intron-variant | CHD3 | GRCh38.p7 | 17:7891098 | ATCCTCGCTAATTGA[C/T]ACTTTTAATTTGAGG | 1107 |
rs370889007 | snp | G/T | 6.639e-05 | 0.00576113 | intron-variant | CHD3 | GRCh38.p7 | 17:7910837 | AACTTCTGCTTCCTC[G/T]CTGTTCCAGGCCTAC | 1107 |
rs370985532 | snp | G/T | 1.6646e-05 | 0.00288491 | missense | CHD3 | GRCh38.p7 | 17:7901283 | GCTTATGAGGGTGGG[G/T]CACTTATTAAGTCGT | 1107 |
rs370987829 | snp | C/T | 1.75081e-05 | 0.00295867 | intron-variant | CHD3 | GRCh38.p7 | 17:7908060 | GCTCCTCAAGGGGAT[C/T]TGCTCATCCTCATGG | 1107 |
rs371191838 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7911419 | ATGAAGTGACGTTTG[A/G]GAGTGATCTGGAGAT | 1107 |
rs371213219 | snp | C/T | 8.2958e-05 | 0.00643988 | intron-variant | CHD3 | GRCh38.p7 | 17:7906827 | CTTCCTGTCTGTAAG[C/T]GCCTGGAGCTGACAC | 1107 |
rs371242969 | snp | A/G | 0.000748874 | 0.0193359 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906720 | TCTTCCTGTCACCCA[A/G]AGAATCAAGCTGGCT | 1107 |
rs371266297 | snp | A/G | 8.42084e-05 | 0.00648823 | intron-variant | CHD3 | GRCh38.p7 | 17:7898972 | ACTGGAGGAGCCGCC[A/G]ACTATTTCCTTGAGC | 1107 |
rs371326639 | snp | C/T | 0.000116549 | 0.00763289 | intron-variant | CHD3 | GRCh38.p7 | 17:7908549 | AAGGAAAAGGTTCTC[C/T]CAAGCTGGCAAAAAA | 1107 |
rs371339515 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905726 | GAGCTGGGCCCAGTG[C/T]TCCTGAGTTCTCCAA | 1107 |
rs371364679 | snp | A/G | 0.000218262 | 0.0104443 | intron-variant | CHD3 | GRCh38.p7 | 17:7894070 | AGGCCTGGGGAGGGC[A/G]TAGAATGAAGTCTGC | 1107 |
rs371432400 | snp | C/G | 5.08023e-05 | 0.0050397 | intron-variant | CHD3 | GRCh38.p7 | 17:7901041 | CCCATTCTCAGAAAA[C/G]ATGGGTGGGGAGTAG | 1107 |
rs371475155 | snp | A/G | 0.0019654 | 0.0312864 | intron-variant | CHD3 | GRCh38.p7 | 17:7900449 | TTGGCAGAGATGAGA[A/G]GTGGAGCAGATAAAA | 1107 |
rs371560913 | snp | C/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7908911 | TTGGAACCTAGGGAA[C/G]GTTAACACCTTCAGG | 1107 |
rs371646549 | snp | A/G | 5.02601e-05 | 0.00501274 | intron-variant | CHD3 | GRCh38.p7 | 17:7898151 | TGACGATGAGGGCAT[A/G]AAAGCCAAAACTCCA | 1107 |
rs371657909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7902187 | GCACTTTGGGAGGCC[A/G]AGGCAGGAAGATCAC | 1107 |
rs371852488 | snp | A/G | 4.94548e-05 | 0.00497242 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905831 | TAGACATTTGTCGCC[A/G]TTGCCTCCTTGCTCC | 1107 |
rs371860721 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893340 | TAAGATGATGACCAT[C/T]CTTGGGGCCAAATGG | 1107 |
rs371864899 | snp | C/T | 8.24599e-05 | 0.00642053 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7911531 | GGCATTGGTGTCAGA[C/T]GGGCTGGATCGGAAG | 1107 |
rs371870070 | snp | C/T | 3.30066e-05 | 0.00406229 | intron-variant | CHD3 | GRCh38.p7 | 17:7900745 | AAGTAAGATGCAAGA[C/T]GAGCTGCCTGGAGTA | 1107 |
rs371903095 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912218 | TACCTCCTGTGTACC[A/G]GCATCTTGTGTTGGG | 1107 |
rs371908467 | snp | A/G | | | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888949 | GAAGGTAGGTTTTAG[A/G]CTACTTGGGAGGAGG | 1107 |
rs371914243 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7897957 | GCTCCTCCCCATGGC[C/T]TCCTGCCCCACAGTG | 1107 |
rs371956540 | snp | C/T | 6.63097e-05 | 0.00575764 | intron-variant | CHD3 | GRCh38.p7 | 17:7895323 | TTCCTCCTCCTTGTA[C/T]GTGTCCATCCCAAAG | 1107 |
rs371961138 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | CHD3 | GRCh38.p7 | 17:7895467 | CCGTCCTCTTCAAGG[C/T]AGATCAGAGCGAGAG | 1107 |
rs371964265 | snp | A/G | 3.32458e-05 | 0.00407698 | intron-variant | CHD3 | GRCh38.p7 | 17:7903999 | AAGACAAGGTGAGAG[A/G]CTTTGGGGGCCAGAC | 1107 |
rs372004415 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7890560 | ATGTTATTTTTATTT[C/G]TTTCTCTTAGGACAG | 1107 |
rs372031314 | snp | A/G | 0.000152683 | 0.00873604 | synonymous-codon, intron-variant | CHD3 | GRCh38.p7 | 17:7907641 | GGGGGAGGAGAAGCC[A/G]TTGGATGGACAGGAA | 1107 |
rs372057201 | snp | C/T | 1.65759e-05 | 0.00287883 | intron-variant | CHD3 | GRCh38.p7 | 17:7898493 | GACCCACTCTTTTTC[C/T]AGAGAACTAATTATG | 1107 |
rs372075169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885594 | GCGAGCGCCCCTCGG[C/G]CTCTGGCCCCGGTGG | 1107 |
rs372099051 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7908769 | CGAGCCATTTAAAAC[C/T]GAAGCCAATAAGGGG | 1107 |
rs372129891 | snp | A/G | 9.42907e-05 | 0.0068656 | synonymous-codon, intron-variant | CHD3 | GRCh38.p7 | 17:7907611 | CACAGCCACAGAGTC[A/G]ACGCCAGGAGAAAGG | 1107 |
rs372182228 | snp | A/C/T | 0.000424634 | 0.0145649 | intron-variant | CHD3 | GRCh38.p7 | 17:7893260 | CATCTGTGAAGGGTC[A/C/T]GAGTTTTCTGCTTCT | 1107 |
rs372184527 | snp | A/G | 1.6507e-05 | 0.00287284 | intron-variant | CHD3 | GRCh38.p7 | 17:7900249 | CGGTCACTTGTCACT[A/G]ATAAGCCCATTTTCC | 1107 |
rs372303142 | snp | A/G | 0.000214297 | 0.010349 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905821 | CTAAGAACCCTAGAC[A/G]TTTGTCGCCATTGCC | 1107 |
rs372355101 | snp | A/T | 0.000329951 | 0.01284 | missense | CHD3 | GRCh38.p7 | 17:7894167 | CTGAGGAATCAGACC[A/T]GGACAGTGGCAGTGT | 1107 |
rs372355352 | snp | A/C/G | 0.000100138 | 0.00707535 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903274 | CTTGCCCCTGCAGGC[A/C/G]TTTAGCCGGGCTCAT | 1107 |
rs372356169 | in-del | -/CTGAGTGAAATGGGAG | 0.0759472 | 0.179459 | intron-variant | CHD3 | GRCh38.p7 | 17:7900188 | TTGGGGCCTCTGATC[-/CTGAGTGAAATGGGAG]CTGGGGCAGGGAAAG | 1107 |
rs372395250 | snp | A/G | 0.000181403 | 0.009522 | missense | CHD3 | GRCh38.p7 | 17:7911532 | GCATTGGTGTCAGAC[A/G]GGCTGGATCGGAAGG | 1107 |
rs372490885 | snp | C/G | 1.64944e-05 | 0.00287175 | missense | CHD3 | GRCh38.p7 | 17:7907205 | AAACCAGGAGGAAAA[C/G]CCAGAGAAGAACAGC | 1107 |
rs372516847 | snp | A/G | 1.67587e-05 | 0.00289466 | intron-variant | CHD3 | GRCh38.p7 | 17:7894284 | AGGAGTGTTGACTGT[A/G]TGTGATCCTGTCAGT | 1107 |
rs372542068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904908 | AGACTGAAGGTGGGC[A/G]GTGAATGGAGATGGT | 1107 |
rs372551921 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7894366 | CTCCCTCTCTCTCTC[C/T]ATCTCCCCCTGCCCT | 1107 |
rs372603459 | snp | C/G | 3.30557e-05 | 0.00406531 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910474 | CATGAAGGCGGACGT[C/G]ACCCGCCTGCCAGCC | 1107 |
rs372684707 | snp | C/G | 1.6599e-05 | 0.00288084 | intron-variant | CHD3 | GRCh38.p7 | 17:7900997 | GTGGCTGCTATGGTA[C/G]ATACACAGAGCAGGG | 1107 |
rs372699348 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7894746 | GTCTAGGATCCTAAT[A/G]TATTCCTTTCTCCCA | 1107 |
rs372716915 | snp | C/T | 4.9458e-05 | 0.00497258 | missense | CHD3 | GRCh38.p7 | 17:7893822 | CCAGGCCATAAGAGG[C/T]GGAGTAAGAGCCCCC | 1107 |
rs372722431 | snp | C/T | 4.95814e-05 | 0.00497878 | intron-variant | CHD3 | GRCh38.p7 | 17:7900782 | TCCTGACTCGAAAT[C/T] | 1107 |
rs372740033 | snp | C/T | 1.65853e-05 | 0.00287964 | intron-variant | CHD3 | GRCh38.p7 | 17:7906819 | GACTGGAGCTTCCTG[C/T]CTGTAAGCGCCTGGA | 1107 |
rs372752099 | snp | C/T | 5.07352e-05 | 0.00503637 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903227 | TGGGCAGCTTCTCCC[C/T]GGCCACTCCCCTGAC | 1107 |
rs372817877 | snp | A/G | 0.00228073 | 0.0336922 | intron-variant | CHD3 | GRCh38.p7 | 17:7907304 | GGGGCTTGGAGGCCA[A/G]GTACCTGGGAGCCCT | 1107 |
rs372837121 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905440 | GTTAATTTTAAAATA[C/T]GACTGGTTCTTTTAG | 1107 |
rs372865492 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890320 | TGTAATCCCAGCTAC[A/G]CAGGAGGCTGAGGCA | 1107 |
rs372870410 | snp | C/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7901655 | AGCTGGGATTACAGG[C/G]GTGCACCACCATGCC | 1107 |
rs372995008 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896660 | TCCACCTGCCTCTGC[C/T]TCCCAAAGTGCTGGG | 1107 |
rs373009202 | snp | C/T | 1.69292e-05 | 0.00290935 | intron-variant | CHD3 | GRCh38.p7 | 17:7894912 | GTCTATCCTTGGCCC[C/T]CTAGGAGAAGGAGGG | 1107 |
rs373061784 | snp | A/C | 5.27941e-05 | 0.00513754 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904636 | TGAGGACTGCCCCAG[A/C]TGCAGGCAGTAAAGG | 1107 |
rs373120724 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7893984 | GGGGCCAAGGATCCA[C/G]AGACAGGGATCCGTG | 1107 |
rs373129711 | snp | A/C/G | 1.65592e-05 | 0.00287738 | intron-variant | CHD3 | GRCh38.p7 | 17:7897305 | CACAGGTGAATCCTC[A/C/G]GTCCCTGGGAAGTCA | 1107 |
rs373177060 | snp | C/T | 0.000396151 | 0.0140683 | intron-variant | CHD3 | GRCh38.p7 | 17:7899339 | CCCCATTCTTGACTC[C/T]CAGGGCCACACAAAA | 1107 |
rs373299963 | snp | C/G/T | 0.000247374 | 0.0111188 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7897271 | GCCAGAGTGGATGAC[C/G/T]GTCCACCGCATCATC | 1107 |
rs373305007 | snp | A/G | 4.94336e-05 | 0.00497135 | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888996 | TGGAGACTTTCTCCT[A/G]TGTGATGAAGGCGGC | 1107 |
rs373317251 | snp | C/T | 3.30327e-05 | 0.0040639 | intron-variant | CHD3 | GRCh38.p7 | 17:7907085 | AGCCAGGAGTCAGGG[C/T]GGGAGAATCTCTGTC | 1107 |
rs373501967 | snp | A/G | | | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7911486 | CAACGGCCCTCCAGT[A/G]CTTGTGAAGAAGGAG | 1107 |
rs373633288 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906519 | ACCCCTTCTGTGGCT[C/T]CCCTAACCCTCCTCC | 1107 |
rs373721338 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | CHD3 | GRCh38.p7 | 17:7907119 | ATCACTGTGCCTTCC[C/T]CTGCAGCTACTCCAG | 1107 |
rs373796359 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7899044 | ACTCAGCCACGGTTT[A/G]TCACAGCCACTGGAG | 1107 |
rs373961013 | in-del | -/GA | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896905 | TCAGGTGATCCACCC[-/GA]GCCTGAGCCTCCTAA | 1107 |
rs374056403 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896803 | ATCTGGGATTACAGG[C/T]GTGCGCCACCACACC | 1107 |
rs374057098 | snp | C/G | 0.000302069 | 0.0122859 | intron-variant | CHD3 | GRCh38.p7 | 17:7908351 | TGTCTGTTGGACTGA[C/G]TGCAGTCTGCAAAAC | 1107 |
rs374162321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7892435 | AAAAGTAAAGCATTT[C/T]TGTTGATTTTATTTT | 1107 |
rs374255213 | snp | C/T | 0.00010143 | 0.00712073 | intron-variant | CHD3 | GRCh38.p7 | 17:7898447 | GTTCAGAAAAGAAAG[C/T]GTAGGACTCCCAAGG | 1107 |
rs374279225 | snp | C/T | 9.89087e-05 | 0.00703168 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905843 | GCCATTGCCTCCTTG[C/T]TCCCACCCTCAGGTG | 1107 |
rs374284825 | snp | C/G | 1.64787e-05 | 0.00287038 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894491 | GGATTACTGTGAGGT[C/G]TGCCAGCAGGGTGGG | 1107 |
rs374315497 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905723 | TGAGAGCTGGGCCCA[C/G]TGTTCCTGAGTTCTC | 1107 |
rs374331164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7891832 | CACCACTGCTATGCT[C/T]TAGCCTGGGCAACAA | 1107 |
rs374375497 | snp | A/G | 3.29495e-05 | 0.00405877 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905171 | CGTCCTGAAGGTGGC[A/G]TCTGTGTTCCTGACT | 1107 |
rs374396701 | snp | C/T | | | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903156 | GTCAGAAATAAATCT[C/T]TTCTGGGAGGAGAGA | 1107 |
rs374431308 | snp | A/T | 1.64844e-05 | 0.00287087 | splice-acceptor-variant | CHD3 | GRCh38.p7 | 17:7890938 | AAGCCCCTCTCCCGC[A/T]GCAAGTGGAACAGAA | 1107 |
rs374434743 | snp | C/T | 3.32851e-05 | 0.00407939 | intron-variant | CHD3 | GRCh38.p7 | 17:7894108 | ACGGCCACGGGGCTA[C/T]GGGCAGTATGTTTTT | 1107 |
rs374465330 | snp | A/G | 1.67494e-05 | 0.00289386 | missense | CHD3 | GRCh38.p7 | 17:7910901 | GGGGCGGCCTTCAGC[A/G]CCGCACCCGTAGGGG | 1107 |
rs374490245 | snp | A/G | 1.68015e-05 | 0.00289836 | intron-variant | CHD3 | GRCh38.p7 | 17:7907305 | GGGCTTGGAGGCCAG[A/G]TACCTGGGAGCCCTC | 1107 |
rs374527023 | snp | A/G | 3.35762e-05 | 0.00409719 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903249 | TCCCCTGACCCACCC[A/G]CCACTTTCTCTTGCC | 1107 |
rs374548787 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884457 | ACTTTTATATATATA[C/T]ATATATATATATATA | 1107 |
rs374560554 | snp | C/T | 0.000350693 | 0.0132372 | synonymous-codon, intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7884932 | GGCGGCCGACGAGGA[C/T]GATGAGGAGGACGAC | 1107 |
rs374672105 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CHD3 | GRCh38.p7 | 17:7910088 | CTTGCTCTTCCAGTA[A/T]GAGATGTTCTGACAA | 1107 |
rs374750174 | snp | A/G | 4.94588e-05 | 0.00497262 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905828 | CCCTAGACATTTGTC[A/G]CCATTGCCTCCTTGC | 1107 |
rs374915623 | snp | A/G | 3.30131e-05 | 0.00406269 | missense | CHD3 | GRCh38.p7 | 17:7910457 | GAGGAGTTGCTGAGC[A/G]ACATGAAGGCGGACG | 1107 |
rs374932223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7887904 | CCGTTCTCGCTTTGC[C/G]TCTCCCGCCACCGAC | 1107 |
rs374961455 | snp | A/G | 0.000100293 | 0.00708069 | intron-variant | CHD3 | GRCh38.p7 | 17:7894095 | GTCTGCCTCACTGAC[A/G]GCCACGGGGCTATGG | 1107 |
rs375140887 | snp | G/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7900236 | TGATGCTGTGGGTCG[G/T]TCACTTGTCACTAAT | 1107 |
rs375165452 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7906886 | GCAGGAGTTTGAGCA[C/T]ATCAATGGGCGTTGG | 1107 |
rs375174125 | snp | C/T | 1.69772e-05 | 0.00291347 | intron-variant | CHD3 | GRCh38.p7 | 17:7894304 | ATCCTGTCAGTGGGC[C/T]GTCCTCTCATTCTTA | 1107 |
rs375249634 | snp | C/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7907930 | AGCTTCGACCAGGGC[C/G]TCGAGATGAGCCACG | 1107 |
rs375273377 | snp | A/G | 4.9543e-05 | 0.00497685 | intron-variant | CHD3 | GRCh38.p7 | 17:7900774 | TAGGGCTTGGGGATT[A/G]ATGGGAGCGTTCCAA | 1107 |
rs375382219 | snp | A/T | 1.84045e-05 | 0.00303347 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893427 | AGCGGCAGCAGCAGC[A/T]GCAGCTGTAGCTGAG | 1107 |
rs375435771 | snp | C/T | 0.000262824 | 0.0114605 | intron-variant | CHD3 | GRCh38.p7 | 17:7900048 | GGTGAGTGAGGTTTC[C/T]AGACCTAAAAAACTT | 1107 |
rs375455976 | snp | A/C | 0.000336126 | 0.0129595 | intron-variant | CHD3 | GRCh38.p7 | 17:7903774 | AAGCTTTCCCATCAG[A/C]CTTTCTAAACTTTGG | 1107 |
rs375492899 | snp | A/C/G/T | 0.00102711 | 0.022643 | synonymous-codon, missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907626 | GACGCCAGGAGAAAG[A/C/G/T]GGGGAGGAGAAGCCG | 1107 |
rs375549221 | snp | G/T | 1.65162e-05 | 0.00287365 | intron-variant | CHD3 | GRCh38.p7 | 17:7906850 | GCTGACACCTAACCC[G/T]CCCACCCTGCCACCC | 1107 |
rs375597707 | snp | C/T | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7907206 | AACCAGGAGGAAAAG[C/T]CAGAGAAGAACAGCA | 1107 |
rs375616544 | snp | G/T | 1.67654e-05 | 0.00289524 | intron-variant | CHD3 | GRCh38.p7 | 17:7894083 | GCGTAGAATGAAGTC[G/T]GCCTCACTGACGGCC | 1107 |
rs375618387 | snp | A/C | 0.000121083 | 0.00777991 | intron-variant | CHD3 | GRCh38.p7 | 17:7901236 | CCTCCTCTCTCCTCC[A/C]TTTTCAGGAGTCCCC | 1107 |
rs375623755 | snp | A/C | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883833 | CCCTTCTGAAGTATT[A/C]AAAAAAAAAAAAGCT | 1107 |
rs375680472 | in-del | -/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890505 | AGGTAAGATATGGTA[-/T]GTGCTGAGAACAGTT | 1107 |
rs375687314 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905836 | ATTTGTCGCCATTGC[C/T]TCCTTGCTCCCACCC | 1107 |
rs375758304 | snp | C/T | 6.80388e-05 | 0.00583222 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893376 | GTTCAGTGCCAACAA[C/T]CCCTTCAAGGGGTCA | 1107 |
rs375766019 | snp | C/G/T | 6.60659e-05 | 0.0057471 | intron-variant | CHD3 | GRCh38.p7 | 17:7900240 | GCTGTGGGTCGGTCA[C/G/T]TTGTCACTAATAAGC | 1107 |
rs375803477 | snp | A/G | 4.98442e-05 | 0.00499196 | intron-variant | CHD3 | GRCh38.p7 | 17:7899875 | AGGTGGCAGCTGAAT[A/G]GGCAATAATTATGTT | 1107 |
rs375804462 | snp | A/G | 8.93535e-05 | 0.00668347 | intron-variant | CHD3 | GRCh38.p7 | 17:7907564 | TCAGGGGATGAGGGT[A/G]ACATCCTCCCTTCCT | 1107 |
rs375812198 | snp | C/T | 2.63675e-05 | 0.00363085 | intron-variant | CHD3 | GRCh38.p7 | 17:7893248 | GTGTTCCCAGACCAT[C/T]TGTGAAGGGTCCGAG | 1107 |
rs375855082 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885698 | GACAGGCAGAGTGGG[A/G]ACGGTGTCCATCGGA | 1107 |
rs375857053 | snp | C/T | 0.000270805 | 0.0116331 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906101 | AACTGATTATCACCC[C/T]CCCTGTCATACAATA | 1107 |
rs375862903 | snp | C/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7901621 | GTTCAAGTGATTCTC[C/G]TGCCTCAGCCTCCCA | 1107 |
rs375871339 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896280 | CTAATCCCATTCCCT[A/G]TCTCTTGCTTGTAAG | 1107 |
rs375871584 | snp | A/G | 3.29554e-05 | 0.00405914 | missense | CHD3 | GRCh38.p7 | 17:7899176 | ACCATACAAACCATC[A/G]TCTTCCTCTACTCAC | 1107 |
rs375896180 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | CHD3 | GRCh38.p7 | 17:7907160 | GAAAGGAGAAGGCAT[A/G]AGGACACCTCTTGAG | 1107 |
rs375906970 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | CHD3 | GRCh38.p7 | 17:7894993 | AGGAAGAAGGGGAGA[A/G]GGAGGAGGAGGATGA | 1107 |
rs375911820 | in-del | -/GG | | | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912778 | TCTGTTATTTTTTAT[-/GG]GGGGGGGGAGTTTTT | 1107 |
rs375994896 | snp | A/G | 6.75721e-05 | 0.00581219 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903228 | GGGCAGCTTCTCCCC[A/G]GCCACTCCCCTGACC | 1107 |
rs376031813 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CHD3 | GRCh38.p7 | 17:7897336 | GACCTGGTATATGAC[A/G]TTATTCTTACCATGG | 1107 |
rs376096086 | snp | G/T | 8.72588e-05 | 0.00660468 | intron-variant | CHD3 | GRCh38.p7 | 17:7908369 | CAGTCTGCAAAACCC[G/T]GTTACCTCTTCTGTC | 1107 |
rs376140622 | snp | A/G | 0.000165085 | 0.00908378 | synonymous-codon, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905957 | ACAGTGGCTGGTGCG[A/G]GACCTGAGGGGCAAG | 1107 |
rs376154697 | snp | A/G | 0.000123801 | 0.0078667 | intron-variant | CHD3 | GRCh38.p7 | 17:7893278 | GTTTTCTGCTTCTAT[A/G]TTTACAGGCCCCTAA | 1107 |
rs376172907 | snp | C/T | | | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906479 | GGGGTCCTCAGTCAT[C/T]CTCGCGCCTCCCTCA | 1107 |
rs376244221 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896949 | CAGGCATGAGCCACC[A/G]TGCCTGGGCCAATCC | 1107 |
rs376262389 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886848 | CCGGATCTGGGTACG[C/T]TGGGGAGAGAAGCGT | 1107 |
rs376314605 | snp | C/T | 1.64868e-05 | 0.00287109 | intron-variant | CHD3 | GRCh38.p7 | 17:7890937 | AAAGCCCCTCTCCCG[C/T]AGCAAGTGGAACAGA | 1107 |
rs376539763 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7892486 | TTTATTTCGCTGTTT[C/T]TTATTTCCCCTTTTT | 1107 |
rs376604597 | snp | C/T | 9.90491e-05 | 0.00703667 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7911558 | GAAGGAGCCCCGAGC[C/T]GGGGAGGTGATCTGT | 1107 |
rs376648861 | snp | A/G | 0.000265239 | 0.011513 | intron-variant | CHD3 | GRCh38.p7 | 17:7900525 | GGCAAGGAACTTGCC[A/G]ACCTGTTAATTTTCT | 1107 |
rs376670741 | snp | A/T | 2.31849e-05 | 0.00340469 | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890698 | AAAAAAAGGAGAAGA[A/T]GACAAAGCGGCGGAA | 1107 |
rs376674854 | snp | A/G | 1.6857e-05 | 0.00290314 | intron-variant | CHD3 | GRCh38.p7 | 17:7898969 | AAGACTGGAGGAGCC[A/G]CCGACTATTTCCTTG | 1107 |
rs376699870 | snp | A/G | 1.65018e-05 | 0.00287239 | missense | CHD3 | GRCh38.p7 | 17:7898537 | CCCAGCCCCGCAAGT[A/G]TAAGAAGAAGAAGAA | 1107 |
rs376704763 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD3 | GRCh38.p7 | 17:7906935 | CCTGACCCCAGCGCC[A/G]ATTCTAAGCGCTCCT | 1107 |
rs376781469 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7892731 | CCATCTCTTGACCTC[A/G]TGATCCTCCCACCTT | 1107 |
rs376843101 | snp | G/T | 1.64751e-05 | 0.00287007 | missense | CHD3 | GRCh38.p7 | 17:7897206 | AAGCGTAAAGTGAAA[G/T]ACCCGCACTATGCTG | 1107 |
rs376849433 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7893969 | TCTACTAAACACCTG[A/G]GGGCCAAGGATCCAG | 1107 |
rs376918939 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7907559 | TGGGGTCAGGGGATG[A/G]GGGTAACATCCTCCC | 1107 |
rs376928718 | snp | C/T | 0.00080675 | 0.020068 | intron-variant | CHD3 | GRCh38.p7 | 17:7894069 | AAGGCCTGGGGAGGG[C/T]GTAGAATGAAGTCTG | 1107 |
rs377079849 | in-del | -/AT | 0.499154 | 0.0205497 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884458 | CTTTTATATATATAC[-/AT]ATATATATATATATA | 1107 |
rs377081442 | snp | C/T | 4.95651e-05 | 0.00497796 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910491 | CCCGCCTGCCAGCCA[C/T]GCTGTCCCGAATACC | 1107 |
rs377142121 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905182 | TGGCATCTGTGTTCC[C/T]GACTCTACCTCACCT | 1107 |
rs377180914 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7893905 | AATAAAACTAGGGCT[C/T]CTGGGTGGCAAGAGG | 1107 |
rs377213049 | snp | A/G | 4.94858e-05 | 0.00497398 | missense | CHD3 | GRCh38.p7 | 17:7897272 | CCAGAGTGGATGACC[A/G]TCCACCGCATCATCA | 1107 |
rs377216305 | snp | C/G | 1.66023e-05 | 0.00288113 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7906010 | TGTGGGTGATACAGG[C/G]CTGAGTTGGACGCAA | 1107 |
rs377227774 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7909771 | CAGAAACTACCACCC[A/G]TCCAACCCTCTGGCC | 1107 |
rs377390282 | snp | A/T | 0.000123521 | 0.00785782 | intron-variant | CHD3 | GRCh38.p7 | 17:7901400 | GCCCTTAGCTGTCTT[A/T]ACATCTGCTTCCTCT | 1107 |
rs377400905 | snp | C/T | 0.00892714 | 0.0662108 | intron-variant | CHD3 | GRCh38.p7 | 17:7897311 | TGAATCCTCGGTCCC[C/T]GGGAAGTCAGACCTG | 1107 |
rs377410163 | snp | C/G | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7910733 | AGTGAGTCTCCCTGC[C/G]TGTGTATCCTACCCT | 1107 |
rs377459179 | snp | C/G/T | 1.70414e-05 | 0.00291898 | intron-variant | CHD3 | GRCh38.p7 | 17:7911007 | ACCCCCTGCTACTCA[C/G/T]ACTCCTCCTTTGCCA | 1107 |
rs377613189 | snp | C/G | 1.67542e-05 | 0.00289427 | intron-variant | CHD3 | GRCh38.p7 | 17:7894090 | ATGAAGTCTGCCTCA[C/G]TGACGGCCACGGGGC | 1107 |
rs377616621 | snp | A/C/T | 1.73564e-05 | 0.00294583 | intron-variant | CHD3 | GRCh38.p7 | 17:7908046 | TCTCGCTGCTTTCTG[A/C/T]TCCTCAAGGGGATCT | 1107 |
rs377618576 | snp | C/G | 1.65438e-05 | 0.00287605 | intron-variant | CHD3 | GRCh38.p7 | 17:7907037 | TCTAAACCTGGTAAT[C/G]AGAAGTCAGGATGGT | 1107 |
rs377745636 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905059 | GCATGGGCATATCCC[A/G]AGAGCCCTCCCTGAC | 1107 |
rs377747033 | snp | C/T | 1.67449e-05 | 0.00289347 | missense, synonymous-codon | CHD3 | GRCh38.p7 | 17:7910584 | GCACGGAGCCTCACC[C/T]CACACCGGTAACCCT | 1107 |
rs377764206 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7889991 | CTAGTGAAGAGCCTC[A/G]TTGTCAGTGTGTCCT | 1107 |
rs386795056 | multinucleotide-polymorphism | AGA/GCC | | | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885745 | GAGACTTAGGTGCCC[AGA/GCC]AACTGAGGGGCATGC | 1107 |
rs398030272 | in-del | -/AT | 0 | 0 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884476 | TATATATATATATAT[-/AT]GTATATATATATATA | 1107 |
rs527257444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889504 | CATCCCAGAGTACTC[A/G]AAACACTTTCTGTTT | 1107 |
rs527371245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7895281 | CCTATCTTCTCATCT[A/G]ACAATGGGTTCTTTC | 1107 |
rs527382756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7896000 | GGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC | 1107 |
rs527486001 | snp | A/G | | | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907928 | GGAGCTTCGACCAGG[A/G]CCTCGAGATGAGCCA | 1107 |
rs527533831 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7903612 | GCAGCCTTTGAAGGA[A/G]GGAGAGCCTTCTTTT | 1107 |
rs527604195 | snp | C/T | 0.000121925 | 0.00780689 | intron-variant | CHD3 | GRCh38.p7 | 17:7910642 | TTTGTGTTCCTCCTG[C/T]ACACATACAAACACT | 1107 |
rs527760010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7887998 | CCCCTGGCTGGTGGT[A/G]GCCGAGGCCGTGTCC | 1107 |
rs527841730 | snp | A/G | 0.000119034 | 0.00771382 | intron-variant | CHD3 | GRCh38.p7 | 17:7894305 | TCCTGTCAGTGGGCC[A/G]TCCTCTCATTCTTAT | 1107 |
rs527968854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901771 | CCGCCTCGGTCTCCC[A/C]AAGTGCTGGGATTAC | 1107 |
rs527979074 | snp | C/T | 3.36553e-05 | 0.00410201 | intron-variant | CHD3 | GRCh38.p7 | 17:7893974 | TAAACACCTGGGGGC[C/T]AAGGATCCAGAGACA | 1107 |
rs528360894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7893109 | TTAAACCTGTTCTTT[C/T]CCCGCTTTTTTTAAA | 1107 |
rs528374121 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885078 | CGCCGCCGCCCCCGC[C/T]GCCAGGTAAGCGCCC | 1107 |
rs528425139 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885971 | CCCCCGGCTCCACCC[C/G]CTTCATCTCGCCGGG | 1107 |
rs528665292 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912525 | CCTTGTCGTTGGGAC[C/G]AGAGCAAAATAGTGG | 1107 |
rs528724409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906326 | TGACTGATGGGGCCC[A/G]GGAATTAAGTACCAA | 1107 |
rs528871245 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7891277 | AGGGGCGAGGGGTGG[-/A]GGGGCCATCATGATT | 1107 |
rs528910967 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7902426 | ACTCCATCTCAAAAA[A/T]AAATAAAAATAAATA | 1107 |
rs528980487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7908977 | ACCTTGTGCTTGGGA[A/G]TGTGATCTGGGTCAG | 1107 |
rs529270852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886120 | CTCTCTCGCTGAAAC[C/G]ACCCACTCCCTGAGC | 1107 |
rs529399505 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7892386 | TAAGGTGGAATGTAT[G/T]TGAAAGGGTTTTATG | 1107 |
rs529473678 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890166 | CCGGTTGCAGTGGCT[C/T]ACGCCTGTAATCCCA | 1107 |
rs529492744 | snp | A/G | 5.86837e-05 | 0.00541649 | missense, intron-variant | CHD3 | GRCh38.p7 | 17:7907675 | AGGGAGAGGCCGGAG[A/G]GGGAAACAGGGGATT | 1107 |
rs529502448 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7894886 | CCTTAATTTCTTCCA[C/T]CTGTCTGTGTGTCTA | 1107 |
rs529539595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7900140 | TGTAGTCTGGGAGGA[C/T]GTCCAGGTTGGAAGA | 1107 |
rs529870471 | snp | G/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7902792 | TGTGATAGGTCCCTG[G/T]GATGGGAGGGGGACT | 1107 |
rs529883549 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CHD3 | GRCh38.p7 | 17:7901992 | GATGAAAGCTCTGGG[C/T]CTACTCACCAGAAAA | 1107 |
rs529931849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7897721 | GAGGAAAATACTTAG[C/T]GATTAGGTGAACAAA | 1107 |
rs529940017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7898792 | GAGATAGCCCACTGG[A/T]GGCTCTGTCACCAGC | 1107 |
rs529942370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7891267 | CTCTTCACTGAGGGG[C/T]GAGGGGTGGAGGGGC | 1107 |
rs530154285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904902 | GCCCAGAGACTGAAG[A/G]TGGGCGGTGAATGGA | 1107 |
rs530224516 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912105 | TGGCTGCATGTTACC[A/G]TCCCCTACCTCTCCC | 1107 |
rs530396703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7890208 | GGCTGAGCCGGGTAG[A/G]TCATTTGAGGTCAGG | 1107 |
rs530698232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891803 | GAGGCAAAGGTTGTA[A/G]TGAGCCGAGATCACA | 1107 |
rs530781031 | in-del | -/TTAGA | 0.00478085 | 0.0486577 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7912882 | CCTCATTTTTATCTC[-/TTAGA]TTATTCACTAAAACT | 1107 |
rs530902898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905490 | CTGAAGTGCTTGGGA[A/G]AGAATTGGGAGCACC | 1107 |
rs530960516 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7892843 | TGTCACCCAGGCTGC[A/G]CTGCAGTGGTGTGAT | 1107 |
rs530966984 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912104 | GTGGCTGCATGTTAC[C/T]GTCCCCTACCTCTCC | 1107 |
rs531369753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7909008 | GGTTGCTGCTAGGTT[C/T]GCAGTCGGTTTGGAG | 1107 |
rs531419408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7896781 | CTCCTGCCTCAGCCT[C/T]CTGAGTATCTGGGAT | 1107 |
rs531443908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD3 | GRCh38.p7 | 17:7894027 | CCAGAGACAGGGATC[C/T]GTGAGGGATGGCGGA | 1107 |
rs531627725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910703 | CAACTTGCTAGAACA[C/T]AGTCATCACCCTTGA | 1107 |
rs531646922 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904358 | ACCGGATTGGGCTGA[C/T]GCAGCAGAGTAGGGA | 1107 |
rs531758107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888676 | TATCCCTGCTGAAGC[A/G]GGTACAGGCCATCCT | 1107 |
rs531888634 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7895000 | AGGGGAGAAGGAGGA[A/G]GAGGATGATCACATG | 1107 |
rs531888708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888127 | TGCTGGGGCATGGCG[A/C]CTTCCTTGCTGACTT | 1107 |
rs532182608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890378 | AGGTTGCAGTGAGCC[A/G]AGATCACGTCAGTGC | 1107 |
rs532271631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904788 | TACCCAGAGGCCAGG[C/T]GGGTTTGCAGGAGAT | 1107 |
rs532306208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7897595 | GAGACATAATTCATC[C/T]AGACCAGTGTTTTGA | 1107 |
rs532314909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7896838 | TAATTTCTGTATTTT[C/T]AGTAGAGACGGGGTT | 1107 |
rs532336394 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7895606 | ATCCTCTCCCTCTCT[C/T]ACTCCTCTGTTTGTT | 1107 |
rs532405404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904214 | ACAGTGCAGGAGAAA[C/G]ACTGTCAGAGGGATT | 1107 |
rs532681090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888739 | GTGGGTGCGCGCGTG[C/T]GCGCGCGTGCTTTTG | 1107 |
rs532712350 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CHD3 | GRCh38.p7 | 17:7910177 | TTCTTTCTTCTTTCT[C/T]TCCATCTGTCTTCTG | 1107 |
rs532763641 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CHD3 | GRCh38.p7 | 17:7895206 | TGATCCCTTCCCCCA[A/T]CCCTGGGGCCCACAT | 1107 |
rs532929504 | in-del | -/TCTC | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7910204 | TCTGTGGTAATCTGG[-/TCTC]TCTGTCTCTTTTCCT | 1107 |
rs532963368 | in-del | -/T | 0.297636 | 0.24542 | intron-variant | CHD3 | GRCh38.p7 | 17:7901505 | TTCCTCCTGTAAGAG[-/T]TTTTTTTTTTTTTTT | 1107 |
rs533072932 | snp | A/C | 1.67483e-05 | 0.00289377 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903257 | CCCACCCGCCACTTT[A/C]TCTTGCCCCTGCAGG | 1107 |
rs533198288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910048 | CCTCCTGACTATTTC[C/T]TCCCCATCATCCCCA | 1107 |
rs533445310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7907773 | AGTCTGGGGAACCGA[A/T]TGCTTGGGTCCTGGG | 1107 |
rs533889598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888836 | AGATGAATGGGTCAG[G/T]ATATCTGGAACAAAA | 1107 |
rs533981927 | snp | A/G | 0 | 0 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7909184 | GGAGCAGCTGCGGCG[A/G]GCGGCCTACCTGAAC | 1107 |
rs534007194 | snp | C/T | 0 | 0 | intron-variant | CHD3 | GRCh38.p7 | 17:7894653 | CCTGAGGAACCCACC[C/T]ATCTCTTTCCCCCTT | 1107 |
rs534049500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910110 | TTCTGACAACTCCCC[A/G]CCCCCATGTCTTCCA | 1107 |
rs534098059 | snp | C/T | 1.65943e-05 | 0.00288043 | intron-variant | CHD3 | GRCh38.p7 | 17:7902748 | GGAGATACACTGGTC[C/T]CTGGTGGGTGTGGGA | 1107 |
rs534108379 | snp | A/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7910197 | TCTGTCTTCTGTGGT[A/C]ATCTGGTCTCTCTGT | 1107 |
rs534122095 | in-del | -/GGGCCAAGGATCCAGAGACAGGGATCCGTGA | 0.00693446 | 0.0584734 | intron-variant | CHD3 | GRCh38.p7 | 17:7893970 | CTACTAAACACCTGG[lengthTooLong]GGGCCAAGGATCCAG | 1107 |
rs534366813 | snp | C/T | 1.75047e-05 | 0.00295839 | missense | CHD3 | GRCh38.p7 | 17:7907467 | CCTGAACCTGGGTAC[C/T]GTGGGGACAGAGAGA | 1107 |
rs534370609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7899551 | AGATGAAGGTAAGAC[C/T]CTCTACCTCATATCC | 1107 |
rs534426564 | snp | A/G | 0.000280041 | 0.0118297 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7900328 | CAAGATAGATCATAA[A/G]TTGCTGCTGACAGGA | 1107 |
rs534673068 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHD3, NAA38 | GRCh38.p7 | 17:7883299 | TGCTTCTACTTTATC[C/G]GATAGTGTTGGAGAT | 1107 |
rs534808943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7891830 | CACACCACTGCTATG[C/T]TCTAGCCTGGGCAAC | 1107 |
rs534825914 | snp | C/T | | | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7890959 | TGGAACAGAAGTCAT[C/T]AGCAACTCTGCTTCT | 1107 |
rs534961222 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912282 | CCCTACAAAAAGAGT[A/C]ATGGTTGGGTGATAC | 1107 |
rs535053246 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7894005 | GGGATCCGTGAGGGC[C/T]AAGGATCCAGAGACA | 1107 |
rs535106253 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7891302 | ATGATTCCAGTGCTG[A/G]GTTAGAGAACTCTTT | 1107 |
rs535286395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904972 | CAGTGATCTGGTGTT[C/T]CCAGAAGGACCAAGG | 1107 |
rs535323968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7908096 | CTCGTTTTGCCTGAG[A/G]CTTCCTGCTACCTTT | 1107 |
rs535353401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905527 | GTGACAGGAATGTTC[C/T]TGTGTTGTGTATCTT | 1107 |
rs535583020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885587 | CGGCCGCGCGAGCGC[C/T]CCTCGGGCTCTGGCC | 1107 |
rs535728192 | snp | C/T | 0.000399281 | 0.0141238 | missense, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906678 | CCCGCATTGGAGTCA[C/T]GTCTCTCGTCAAAAA | 1107 |
rs535900764 | in-del | -/GG | 0.131717 | 0.227714 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886015 | TGTGTCAAGTGCGGT[-/GG]GGGGGGGGTCCCCCT | 1107 |
rs535937730 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883405 | CTCTTTATCCTAAAA[A/G]TTTGTTGTTTACCCC | 1107 |
rs535989779 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890863 | CAGGGAAGCTAGTGG[A/G]TAGGTAGACAGGCCT | 1107 |
rs536086329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891890 | AGAAAAAATAGTGCC[A/G]ATGTATTTTGTTTTG | 1107 |
rs536132024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890432 | AGACTCCATCTCCAA[A/C]AAAAAAAAGGAGATA | 1107 |
rs536151795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7898149 | TCTGACGATGAGGGC[A/T]TGAAAGCCAAAACTC | 1107 |
rs536155864 | in-del | -/TG | | | downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912794 | GGGGGGGGGAGTTTT[-/TG]GGGGGAGGGATAAGA | 1107 |
rs536172382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7899225 | ATTCTAGGACCTTGA[A/G]GGGGACCGCCTGGAC | 1107 |
rs536279451 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905622 | ATCCCCACCCTCAGG[A/G]CGTAGACAGTCAAAG | 1107 |
rs536422404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7910783 | CTCATAATGTCTCTC[C/T]TACAGCTTCTTTCCT | 1107 |
rs536486989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7903711 | TTCAACATTGGCTCC[C/T]GGGGAAAAAGCCTTC | 1107 |
rs536658411 | in-del | -/TG | 0.0134861 | 0.0810011 | intron-variant | CHD3 | GRCh38.p7 | 17:7896904 | CTCAGGTGATCCACC[-/TG]CGCCTGAGCCTCCTA | 1107 |
rs536705565 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904345 | CAGGAGTGGGGAGAC[C/T]GGATTGGGCTGACGC | 1107 |
rs536773765 | snp | A/T | 1.75434e-05 | 0.00296165 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906742 | AAGCTGGCTGCCTAG[A/T]CTCTGTCCTTCCTCT | 1107 |
rs536820606 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7901883 | GCTGCATGAGGGAAG[C/G]GGGAGGGTGAGCCAT | 1107 |
rs536856099 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904921 | GCGGTGAATGGAGAT[A/G]GTGTAGGATATGCGG | 1107 |
rs536865930 | snp | A/C | | | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7912877 | CTTTTCCTCATTTTT[A/C]TCTCTTAGATTATTC | 1107 |
rs536891389 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912452 | CCTCCTCAAGGCCTG[C/G]ATACAGACTAAATTT | 1107 |
rs537018119 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHD3 | GRCh38.p7 | 17:7891283 | GAGGGGTGGAGGGGC[C/T]ATCATGATTCCAGTG | 1107 |
rs537283612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7896591 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCTCCAT | 1107 |
rs537435704 | snp | A/C | 6.88302e-05 | 0.00586604 | intron-variant | CHD3 | GRCh38.p7 | 17:7890540 | GCAATGGTAGGGATG[A/C]ATAAATGTTATTTTT | 1107 |
rs537697178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7911087 | TCCTTGGTGGTATCC[C/G]GTGTTTTATGGGATA | 1107 |
rs537839026 | snp | C/G/T | 0.00169243 | 0.029042 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904651 | ATGCAGGCAGTAAAG[C/G/T]GGGGAAGTGATGATG | 1107 |
rs537864700 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885346 | GCCGCCGCCGCCGCC[A/G]CCCCGGCTGGAGAGC | 1107 |
rs537870843 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7910782 | GCTCATAATGTCTCT[C/T]CTACAGCTTCTTTCC | 1107 |
rs537883732 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7902962 | CCAACAATTCTGCTT[C/T]CTCCTGTCCACCCGA | 1107 |
rs537969289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910181 | TTCTTCTTTCTCTCC[A/G]TCTGTCTTCTGTGGT | 1107 |
rs538010275 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7888895 | CAAAGGGTATGGCCC[C/G]CTAGTTCCCAAAGGG | 1107 |
rs538054924 | snp | A/G | | | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903116 | AGGAGATGTGGGTTC[A/G]TGGAGGAGGGTGTCA | 1107 |
rs538130217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7887393 | GGAAGCCAAAAACTC[A/G]TTTCTTCTCCCTCCC | 1107 |
rs538134862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7894733 | CAGATGTCCGAGTGT[C/T]TAGGATCCTAATGTA | 1107 |
rs538145400 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888419 | AGCCCAGGCTTTCCC[A/G]TCTTGCATCGGCTGC | 1107 |
rs538237188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7911125 | TCTAGGCTGTCCCCC[A/C]ACCCATCCCTTTCTT | 1107 |
rs538293220 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7909256 | CCGCTTCGCCGAGGC[C/T]GAGTGCCTGGCCGAG | 1107 |
rs538670279 | snp | C/T | 0.000752885 | 0.0193875 | utr-variant-3-prime, missense | CHD3 | GRCh38.p7 | 17:7911661 | CGCTGGGGCCTGCTG[C/T]CAGCCCTCCACCTTC | 1107 |
rs538682977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7895664 | ATTTCAGGCCTGTGG[C/T]CTTCATACCCTACTT | 1107 |
rs538700531 | snp | C/T | 3.29701e-05 | 0.00406005 | synonymous-codon, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903016 | GGCCACTGCTGACAC[C/T]GTCATCATCTTTGAT | 1107 |
rs538700767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910767 | CAGTTGTGGAGTGTG[A/G]CTCATAATGTCTCTC | 1107 |
rs538886081 | snp | A/G | 0.00029883 | 0.0122199 | intron-variant | CHD3 | GRCh38.p7 | 17:7910319 | GTGTTCTCCTCTCTC[A/G]CTCTTTTTCTGCCTG | 1107 |
rs538904585 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7889325 | AGGATGCCAGCTGGC[C/G]AAGTGAGGGGGAAGG | 1107 |
rs539392154 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888226 | GTCCTAGAGTGTCTT[C/T]CTGCACAAGGGGACA | 1107 |
rs539447742 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883055 | CCTCCTTCCTTTGCT[-/C]CATTTGGCAAGGATC | 1107 |
rs539743289 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CHD3 | GRCh38.p7 | 17:7901521 | TTTTTTTTTTTTTTT[G/T]TTTTTTGAGACAGAG | 1107 |
rs539754598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892457 | TTTTATTTTAACCTT[C/T]TATGCTTTTAAGTTT | 1107 |
rs539766410 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7909083 | GCTATGTCCGCCCCC[C/G]CAGCCCCTCACCCAC | 1107 |
rs539894987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7909816 | TTCCCTTTGACCTTC[A/G]ACCTTTCCTCCTACC | 1107 |
rs539992055 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7896159 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 1107 |
rs540011803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885625 | GGTTGGACCGAGGGA[A/G]AGTGGGGTTTCCCCG | 1107 |
rs540122604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892022 | CAATTTCCTCTTCTA[C/T]AAACGGGGAATAATA | 1107 |
rs540148304 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883603 | TCATCGTATCTATTC[A/G]TATCTCTCCCCCAAA | 1107 |
rs540173673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886768 | CCGTCAGGTCCTGCC[A/G]GGGGCTTGGCAGCGC | 1107 |
rs540450812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7887843 | GGCTGCTGAGACCGA[A/G]GTTGGGACTTAGATT | 1107 |
rs540486635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7893753 | GACCTCCATAATTCC[A/G]GGATGTCATGACCTC | 1107 |
rs540601165 | snp | A/G | 0.000283733 | 0.0119074 | intron-variant | CHD3 | GRCh38.p7 | 17:7908529 | TCCTTTGATACACAT[A/G]CAAGAAGGAAAAGGT | 1107 |
rs540609317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7899690 | TACCATCCTAGAGAT[A/G]TGGCAGGTACTCCCA | 1107 |
rs540673801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7893170 | TTTTTCCTAATAGGA[C/T]ATATTCTCACCACCC | 1107 |
rs540697988 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883992 | ACTGATTAATGCCCC[C/T]CCTCAAATATTTTTT | 1107 |
rs540786403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7892099 | GGAAAGCACAGTACC[A/G]TCAGTGCCTGGCTCC | 1107 |
rs540824883 | snp | C/T | 1.6492e-05 | 0.00287154 | intron-variant | CHD3 | GRCh38.p7 | 17:7907109 | CTCTGTCTTTATCAC[C/T]GTGCCTTCCCCTGCA | 1107 |
rs540895315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905230 | CAGTTTGCTTTAAGC[C/T]CACTGTTTTTATACA | 1107 |
rs540931827 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912623 | ATGGCGAACCCCCCA[C/T]TTCCTCTTTGCTGCC | 1107 |
rs541316617 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7901642 | CAGCCTCCCAAGTAG[C/T]TGGGATTACAGGCGT | 1107 |
rs541375224 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885282 | GCGGGGCCAGGCCTC[C/T]TCCCCTCCCCCGCCG | 1107 |
rs541519127 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7884300 | TTATGGAGGGGGTGG[C/T]GGTGCTGGAGGGGGG | 1107 |
rs541531837 | snp | A/C | 0.167484 | 0.23599 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885747 | GACTTAGGTGCCCGC[A/C]AACTGAGGGGCATGC | 1107 |
rs541626286 | snp | C/T | 0.000268853 | 0.0115911 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904130 | TCTTCGTCTAATAGG[C/T]GAGACTGGACTTCAG | 1107 |
rs541627106 | snp | A/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7907820 | AGGCCAGTACAGTAC[A/C]GTACAGATAGTAGTC | 1107 |
rs541777218 | snp | A/C | 3.42524e-05 | 0.00413824 | intron-variant | CHD3 | GRCh38.p7 | 17:7899589 | CCCTCAAAGCTGTCA[A/C]TTCTTTTTCTCAGCC | 1107 |
rs542064329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7898821 | GCTGGCCCTTCCCCA[C/T]GGTGCTGCTGGATAT | 1107 |
rs542378657 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905046 | AGAAAGGGCCTCAGC[A/G]TGGGCATATCCCGAG | 1107 |
rs542443924 | snp | C/T | 4.98178e-05 | 0.00499063 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910867 | CCCGCCGGGTCCCTA[C/T]GCTACACCTCCGGGG | 1107 |
rs542536264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890879 | TAGGTAGACAGGCCT[C/G]TGTGCGGCCTGGAAT | 1107 |
rs542537223 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | CHD3 | GRCh38.p7 | 17:7898952 | CAGGGAGGAAGAGAC[-/T]TAAGACTGGAGGAGC | 1107 |
rs542666404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904719 | GAGAGAAGCCTAGAA[C/G]TCAGAGCCTTCCTCT | 1107 |
rs542675962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890260 | ATGTGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 1107 |
rs542711850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888559 | TGTGGGGTAACTCTC[C/T]GTTCCGTTCCCCAAG | 1107 |
rs542765786 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHD3 | GRCh38.p7 | 17:7896732 | GGTGTGATCTTGGCT[C/T]GCTGCAACCTCCGCC | 1107 |
rs542831891 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | CHD3, NAA38 | GRCh38.p7 | 17:7883259 | TTCTCAGTTCCAGCT[C/T]CTTTCTCTTTCACGG | 1107 |
rs542854910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7911294 | ATGTGTTCAATCATG[G/T]AGCACAAAGTGGAAT | 1107 |
rs542856083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7894862 | TTGCCTGTATCTTCC[A/C]GTTTCATTCCTTAAT | 1107 |
rs542907485 | in-del | -/TTC | 0.00993419 | 0.0697739 | intron-variant | CHD3 | GRCh38.p7 | 17:7910166 | ATGCTCCCTTTTTCT[-/TTC]TTCTTTCTCTCCATC | 1107 |
rs543047934 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896945 | ATTACAGGCATGAGC[C/T]ACCGTGCCTGGGCCA | 1107 |
rs543124572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889157 | CAAAAGGATGTCAGG[C/G]CCCCAGGGTGTTAGT | 1107 |
rs543176013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7898296 | AAGATCTGGCTGAGT[A/G]GTGGAGAAGAGGATG | 1107 |
rs543229386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904743 | TTCCTCTGCTAAAAG[A/G]GAAAGACATAAGGTA | 1107 |
rs543270825 | snp | C/T | 6.66889e-05 | 0.00577408 | intron-variant | CHD3 | GRCh38.p7 | 17:7910360 | TCTGATGCCTCTCTT[C/T]TCCTGGCTCCATCTC | 1107 |
rs543383697 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | CHD3 | GRCh38.p7 | 17:7899298 | GAGGACTAGGGTATA[C/T]GGCCTCTAGCCTAGA | 1107 |
rs543644320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889379 | GAAAGGACCTGCCAC[A/C]GTCAGAGCCCATGGC | 1107 |
rs543662125 | snp | A/T | | | upstream-variant-2KB, intron-variant | CHD3, NAA38 | GRCh38.p7 | 17:7883723 | GCGTTGTGACTTCAA[A/T]GAGGTATGTAGAAAC | 1107 |
rs544120290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7895812 | CTTTTTCCATGTTTT[A/G]TAATATTCCTGGCTG | 1107 |
rs544341173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901699 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 1107 |
rs544711885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7902168 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 1107 |
rs544874007 | in-del | -/ATCAGTTCAGTGCTCTGGAGGC | 0.0162398 | 0.0886349 | intron-variant | CHD3 | GRCh38.p7 | 17:7891925 | AAGGCACTTTAACAT[-/ATCAGTTCAGTGCTCTGGAGGC]ATCAGTTCAGTGCTC | 1107 |
rs545001010 | snp | C/G/T | 0.00125117 | 0.0249821 | intron-variant | CHD3 | GRCh38.p7 | 17:7903815 | TCCCGTTTGTTTTCC[C/G/T]TCTCACCAGGGGAGA | 1107 |
rs545087696 | snp | C/G | 1.6636e-05 | 0.00288405 | intron-variant | CHD3 | GRCh38.p7 | 17:7910824 | ATGAACTAACTCCAA[C/G]TTCTGCTTCCTCTCT | 1107 |
rs545125140 | snp | A/G | 3.30491e-05 | 0.00406491 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7894225 | CCCTGTCCGCACCAA[A/G]AAACTAAAGAGAGGC | 1107 |
rs545172901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901730 | TGGTCAGGATGGTCT[C/T]CATCACCTGACCTCA | 1107 |
rs545292775 | snp | C/T | 3.29533e-05 | 0.00405901 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7899163 | GGGGCTAGGCAAGAC[C/T]ATACAAACCATCGTC | 1107 |
rs545300637 | in-del | -/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7889259 | CCCCACTCCAAGTGC[-/T]TGGGGTCAGGCCAGG | 1107 |
rs545411416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888517 | GCCCCAGGGCCCCAG[A/G]TCTGTGGGGCATCCT | 1107 |
rs545424519 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892818 | TTTTTTTAAAGACAG[A/C/G]GTCTCATTCTGTCAC | 1107 |
rs545494344 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886499 | GGCTTCTGTGGCAAA[A/C]GTTCCTGTCTAGCCG | 1107 |
rs545792526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892976 | TTGTAGAGACAGGAT[C/G]TCACTTTGTTGCCCA | 1107 |
rs545989391 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886140 | CTCCCTGAGCACGTT[-/G]GGGGGGCGTGAACTG | 1107 |
rs546126626 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7908236 | ATTCTTAATTCTAAC[A/G]AACCTGGTTAGAACT | 1107 |
rs546196544 | snp | A/G | 0.00127284 | 0.0251953 | intron-variant | CHD3 | GRCh38.p7 | 17:7907048 | TAATCAGAAGTCAGG[A/G]TGGTGGGAGAGACAG | 1107 |
rs546425369 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913062 | AACTGCCTTCCAGCC[A/T]TCCTTTTGATCATCC | 1107 |
rs546657180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892294 | GTCCTACGGAAGCCC[A/G]TCTTCAGGGCCCATG | 1107 |
rs546826554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7897456 | TTTCCTCCAGGGGAA[C/T]GGGAGAAAACAGGAG | 1107 |
rs547083157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7899837 | AAGGTGTCTGGTTCT[A/G]GAGGTGTAGGTGCAT | 1107 |
rs547199678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CHD3, SCARNA21 | GRCh38.p7 | 17:7906456 | GCACCTGGGGATTTG[A/G]GGGTTTGGGGGTCCT | 1107 |
rs547255382 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | CHD3 | GRCh38.p7 | 17:7896905 | CTCAGGTGATCCACC[A/C]GCCTGAGCCTCCTAA | 1107 |
rs547379667 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912296 | TAATGGTTGGGTGAT[A/G]CTCCCTCAAGCCAAA | 1107 |
rs547391394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7896259 | AAAAAAAAATTCTCA[A/G]TGTTTCTAATCCCAT | 1107 |
rs547391462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904853 | GACACCCAGGGCCAT[G/T]GCTTAGAGTAGGTTT | 1107 |
rs547550790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7890400 | CGTCAGTGCACTCCA[G/T]CATGGGTGACAGAGC | 1107 |
rs547661585 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890228 | TTGAGGTCAGGAGTT[C/T]GCGACAAGCCTGGCC | 1107 |
rs547731994 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886850 | GGATCTGGGTACGTT[G/T]GGGAGAGAAGCGTGA | 1107 |
rs547946842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7903138 | AGGGTGTCATGTTCC[A/G]GGGTCAGAAATAAAT | 1107 |
rs548045552 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7911372 | ACGGGAAGTGGCAGG[A/G]GGTGACCTAGAAGTG | 1107 |
rs548066850 | in-del | -/TGAAG | 0.00358779 | 0.0422022 | intron-variant | CHD3 | GRCh38.p7 | 17:7911405 | AATTCACCATTGTCA[-/TGAAG]TGACGTTTGAGAGTG | 1107 |
rs548099534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891752 | TGTAATCCCAGCTAC[A/T]CGGGAGGCTAAGGCA | 1107 |
rs548315794 | snp | A/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7896616 | CTCCATGTTGATCAG[A/G]CTGGTCTCGAACTCC | 1107 |
rs548363002 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912110 | GCATGTTACCGTCCC[C/T]TACCTCTCCCCACGT | 1107 |
rs549058391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB, missense | CHD3 | GRCh38.p7 | 17:7888860 | AACAAAATATGGAGG[A/T]GAAGGGTGAGATCGG | 1107 |
rs549120809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910124 | CGCCCCCATGTCTTC[C/T]AATGTCCCCCCATCT | 1107 |
rs549222344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7893996 | CCAGAGACAGGGATC[C/T]GTGAGGGCCAAGGAT | 1107 |
rs549229374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7910659 | CACATACAAACACTT[A/C]CATCAGAATCCTATA | 1107 |
rs549244419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7895286 | CTTCTCATCTAACAA[C/T]GGGTTCTTTCTGCCT | 1107 |
rs549285703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7894355 | CTTCAACCCTTCTCC[C/T]TCTCTCTCTCCATCT | 1107 |
rs549431382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7887326 | TCTCCAGTCTCCTTA[C/T]ATTGTTAAACGTTTA | 1107 |
rs549525057 | snp | G/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890562 | GTTATTTTTATTTCT[G/T]TCTCTTAGGACAGTG | 1107 |
rs549585199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888059 | CACTGCCTCGGCAGC[C/T]TGCGTTTCCATGTTC | 1107 |
rs549736592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7887554 | AACCCACCCCCTGCC[C/T]GCAGTACGCATGTGC | 1107 |
rs549748291 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHD3 | GRCh38.p7 | 17:7896783 | CCTGCCTCAGCCTCC[G/T]GAGTATCTGGGATTA | 1107 |
rs549767831 | snp | A/G | 0.000400147 | 0.0141391 | synonymous-codon, missense | CHD3 | GRCh38.p7 | 17:7910891 | TCCGGGGTACGGGGC[A/G]GCCTTCAGCGCCGCA | 1107 |
rs549772047 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7905933 | GCCACCACAGGATGC[C/T]TTCACCACACAGTGG | 1107 |
rs549863623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7890353 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 1107 |
rs549909671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7903576 | ATCAGCCCCCTGGGG[A/T]GAGAAAAACAACTCT | 1107 |
rs549924598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7896089 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT | 1107 |
rs549931005 | snp | C/G | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904768 | AAGGTAGAGTCATTA[C/G]GAACTACCCAGAGGC | 1107 |
rs550038952 | snp | C/T | 6.7365e-05 | 0.00580327 | missense, utr-variant-5-prime | CHD3 | GRCh38.p7 | 17:7889765 | GGAAAACCCCGAAAA[C/T]GCAAGAAGCGTGTAA | 1107 |
rs550086127 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888689 | GCAGGTACAGGCCAT[A/C]CTCTGGATTTGTGGG | 1107 |
rs550329451 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7897621 | TTTGAATGTTTCTTC[C/T]TCATAGTACTTATTA | 1107 |
rs550536142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7902430 | CATCTCAAAAAAAAA[A/T]AAAAATAAATAAAAA | 1107 |
rs551054331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7893227 | AATTGATGAGGGGAG[A/G]TGGCAGTGTTCCCAG | 1107 |
rs551069521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888262 | TGCTGGAGTTAGCAG[A/G]AAAGGTGGCACTGAA | 1107 |
rs551117701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886138 | CCACTCCCTGAGCAC[A/G]TTGGGGGGCGTGAAC | 1107 |
rs551155540 | snp | C/G | 1.64923e-05 | 0.00287156 | missense | CHD3 | GRCh38.p7 | 17:7894558 | CACCTCGTCTGCCTT[C/G]ATCCTGAGCTTGACC | 1107 |
rs551335813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7895222 | CCCTGGGGCCCACAT[A/G]TCCAGCTTTTCATTT | 1107 |
rs551456071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHD3 | GRCh38.p7 | 17:7888185 | ACCCGGGCTCTGGCA[A/G]CCACCCCCCTGCACA | 1107 |
rs551621099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7901141 | AGGAGGAATTGGGAA[C/T]ATGTGGAAGCTGGAT | 1107 |
rs551660142 | snp | C/T | 2.00616e-05 | 0.00316708 | missense | CHD3 | GRCh38.p7 | 17:7893465 | CAGCTGCTGTCTCGT[C/T]GGCCACCCCCATAGC | 1107 |
rs551728877 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7909086 | ATGTCCGCCCCCCCA[G/T]CCCCTCACCCACTGC | 1107 |
rs551749460 | snp | A/G | 5.12869e-05 | 0.00506368 | missense | CHD3 | GRCh38.p7 | 17:7907353 | ATTGTCCTCTTCCAG[A/G]CTGATGCCCCCAGCC | 1107 |
rs551755893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7907810 | GCTGTTTGAAAGGCC[A/G]GTACAGTACAGTACA | 1107 |
rs551760461 | snp | C/T | | | intron-variant | CHD3 | GRCh38.p7 | 17:7890351 | GGAGAATCGCTTGAA[C/T]CCGGGAGGTGGAGGT | 1107 |
rs552043900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7886355 | ATCTGGGTGTCCACA[C/T]CCCCTGCTTGGGGAA | 1107 |
rs552066058 | snp | C/T | 0.00159617 | 0.0282053 | missense, intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885045 | CGCCGCCGCCGCCGC[C/T]GCCACCGCTGCCCCC | 1107 |
rs552152266 | in-del | -/TTG | 0.000798403 | 0.0199641 | downstream-variant-500B | CHD3, LOC284023 | GRCh38.p7 | 17:7913257 | CTTCCTTGATGTTTA[-/TTG]TTCACTAAACAGAGC | 1107 |
rs552155964 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CHD3 | GRCh38.p7 | 17:7900251 | GTCACTTGTCACTAA[A/T]AAGCCCATTTTCCTG | 1107 |
rs552267142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7898954 | AGGGAGGAAGAGACT[A/G]AGACTGGAGGAGCCG | 1107 |
rs552326735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7891810 | AGGTTGTAGTGAGCC[A/G]AGATCACACCACTGC | 1107 |
rs552535984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7892706 | TTCGCCATGTTGGCC[A/G]GGATGGTCTCCATCT | 1107 |
rs552604306 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD3 | GRCh38.p7 | 17:7897892 | GTTTGCTGATAATTG[C/T]GTTTCTCAGGCCTTC | 1107 |
rs552677359 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904769 | AGGTAGAGTCATTAG[A/G]AACTACCCAGAGGCC | 1107 |
rs552739367 | snp | A/G | 0.167484 | 0.23599 | intron-variant, upstream-variant-2KB | CHD3, NAA38 | GRCh38.p7 | 17:7885745 | GAGACTTAGGTGCCC[A/G]CCAACTGAGGGGCAT | 1107 |
rs552797133 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | CHD3 | GRCh38.p7 | 17:7912260 | CTCCCTAGGGACCAA[C/G]GACCACCCCTACAAA | 1107 |
rs552866069 | snp | A/C | | | intron-variant | CHD3 | GRCh38.p7 | 17:7891299 | ATCATGATTCCAGTG[A/C]TGGGTTAGAGAACTC | 1107 |
rs553139119 | snp | A/G | 3.54384e-05 | 0.00420927 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7907484 | TGGGGACAGAGAGAA[A/G]TCAGGTGGGTGCATG | 1107 |
rs553265544 | snp | C/G | | | intron-variant | CHD3 | GRCh38.p7 | 17:7889309 | TCCCCAGTTCCTGGG[C/G]AGGATGCCAGCTGGC | 1107 |
rs553334422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7891350 | AGGACAGAATATAGT[A/G]AGCCCTCCCCTGCCC | 1107 |
rs553351569 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | CHD3 | GRCh38.p7 | 17:7912718 | CCCTCTTCTGTATCA[A/G]GTTTATTGGTTGTAC | 1107 |
rs553388796 | snp | C/T | | | missense | CHD3 | GRCh38.p7 | 17:7906975 | CCTCTCCTACCAAAA[C/T]GTCTCCCACCACTCC | 1107 |
rs553487892 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, missense | CHD3 | GRCh38.p7 | 17:7911696 | CCCCTTGGGCCATCA[A/C]TGGGCTAGGAACCCC | 1107 |
rs553587846 | snp | A/G | 3.29794e-05 | 0.00406061 | synonymous-codon | CHD3 | GRCh38.p7 | 17:7898082 | ATACGAAGAACATAA[A/G]CAAAGCTACTGGAGA | 1107 |
rs553732886 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHD3 | GRCh38.p7 | 17:7895684 | ATACCCTACTTGCTT[A/T]GTTTCCATATGTGGT | 1107 |
rs553750734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7889904 | GAGGCTTGATCCCCC[A/G]GGCCCCCCACTTCCC | 1107 |
rs553797455 | snp | A/T | 3.68548e-05 | 0.00429256 | intron-variant, upstream-variant-2KB | CHD3, SCARNA21 | GRCh38.p7 | 17:7904656 | GGCAGTAAAGGGGGG[A/T]AGTGATGATGAGTAG | 1107 |
rs553820672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD3 | GRCh38.p7 | 17:7903668 | TCTTTCTTTGCCTGT[A/C]GGGTTAAAACAAACA | 1107 |