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 |