SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8550 | snp | A/G | 0.281049 | 0.248064 | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259382 | ACCTCGGGGTGGGGA[A/G]CCCAGCACTGGACAA | 25807 |
rs9537 | snp | A/G | 0.460589 | 0.13473 | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259427 | AGGCAAGAAGCCCCC[A/G]GTGATCCAGTCAGAG | 25807 |
rs710196 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259455 | CCTCAGTTCTTCCCT[C/T]TGAGCCCCCAGGCCC | 25807 |
rs710197 | snp | C/T | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259448 | CTTCTTGCCTCAGTT[C/T]TTCCCTCTGAGCCCC | 25807 |
rs879580 | snp | A/G | 0.39267 | 0.205293 | synonymous-codon, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263971 | CATGCTGGCTGGGGA[A/G]GGACACCGCCCTAGA | 25807 |
rs2231392 | snp | C/T | 0.000363522 | 0.013477 | utr-variant-5-prime, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268334 | CCGTGGACGCCATTT[C/T]CTCTCCTTCCTCCTC | 25807 |
rs2231393 | snp | A/G | | | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29264078 | GCCTCAGCCCTGCTC[A/G]CCCTGGCTTCTGGGC | 25807 |
rs2231394 | snp | C/T | 0.00471251 | 0.048312 | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263964 | GCTGGGGAGGGACAC[C/T]GCCCTAGACGGCCCC | 25807 |
rs2231395 | snp | A/G | 0.0398948 | 0.135484 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263808 | CTGAGCCCAGGGCCC[A/G]TGGGGATGTGTGGGT | 25807 |
rs2231396 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263726 | GCAATACCAAGGAGC[C/T]GTGCACACACATTCC | 25807 |
rs2231397 | snp | A/G | 0.00420551 | 0.0456625 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260717 | AGCTGCCTGTCACCC[A/G]TCCTGCCGGAGTGAG | 25807 |
rs2231398 | snp | A/C | 0.410659 | 0.191543 | synonymous-codon, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260400 | GGAGGGCATCCAGGC[A/C]TCGCTTCTTGACGGG | 25807 |
rs2231399 | snp | C/T | 0.00441643 | 0.0467837 | synonymous-codon, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260156 | CCGTGTGGAGGGTGC[C/T]GTGTCACTGTTGGTT | 25807 |
rs2272902 | snp | A/G | 0.000647794 | 0.0179855 | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29264110 | TGCAGGAATCTCAGC[A/G]TGCCCAGGTGGCACT | 25807 |
rs2301290 | snp | A/G | 0.329783 | 0.236927 | intron-variant, upstream-variant-2KB | RHBDD3 | GRCh38.p7 | 22:29265352 | CCTGTCTAAGGCCAT[A/G]CTTTCCCGGGACACT | 25807 |
rs2301291 | snp | A/G | 0.486332 | 0.08153 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268434 | GGGCTTGGCTGGGAA[A/G]ACTGAGTGGAGTTGC | 25807 |
rs2857460 | snp | C/T | 0.207559 | 0.246371 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268917 | TCTGGCGCTGCCGAG[C/T]TGCCCCCTCTGTGGC | 25807 |
rs2857466 | snp | C/T | 0.487305 | 0.0786545 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29261615 | ttaaaaaaaaaaTCT[C/T]AGAAGCAGAACACCA | 25807 |
rs3204856 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259542 | CAAATGCTTGTGACA[A/G]ATGCCAGGAGGTAGA | 25807 |
rs4505624 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262745 | gaagtctcgctctct[C/T]gcccaggctggagtg | 25807 |
rs5763119 | snp | A/G | 0 | 0 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262738 | ttgagaggaagtctc[A/G]ctctctcgcccaggc | 25807 |
rs5763120 | snp | G/T | 0.000399281 | 0.0141238 | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263889 | AGGGTGGCTCAGAGC[G/T]GAGCAGTGGGGTCAG | 25807 |
rs9613850 | snp | C/G | 0 | 0 | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263885 | AGGAAGGGTGGCTCA[C/G]AGCTGAGCAGTGGGG | 25807 |
rs11539373 | snp | C/T | 0.0217236 | 0.101931 | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267762 | GCCTTTCGGGGTTGC[C/T]GGGCGCGCTCTGCAG | 25807 |
rs11703074 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29270009 | acataagtaatctgg[G/T]ccttagtttcctttc | 25807 |
rs11912931 | snp | C/G | 0.0513262 | 0.151752 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | EMID1, RHBDD3 | GRCh38.p7 | 22:29259864 | TGCTGCCTCCAAGGA[C/G]GTCCAGGTTGAAAAA | 25807 |
rs13058014 | snp | C/G | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29260283 | GTCAGGGCCACCCCG[C/G]CCCCTATACCAGGGG | 25807 |
rs16987345 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259506 | ATGGGGACATGGAGA[A/G]GAAGGGGCCGCCTAC | 25807 |
rs34091309 | snp | A/C | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268888 | TCATCCTTAAGACCC[A/C]GTCGGCTGGGGCGTC | 25807 |
rs34614149 | in-del | -/T | 0.479502 | 0.0991411 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262140 | ATAATTTTGTACGGC[-/T]TTTTTTTTTTTTTTT | 25807 |
rs35098478 | in-del | -/T | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262143 | AATTTTGTACGGCTT[-/T]TTTTTTTTTTTTTTT | 25807 |
rs35125319 | in-del | -/C | 0.000188427 | 0.00970453 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29260683 | CACCTGGACTGGCAT[-/C]CCCCCCCATCACCCT | 25807 |
rs35726449 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260761 | CGGGGTGGCAAGGAG[-/C]CTCAGGGGCCAGCAC | 25807 |
rs35850999 | in-del | -/A | | | frameshift-variant, intron-variant | RHBDD3 | GRCh38.p7 | 22:29264058 | GCCAGCAGCACTGCC[-/A]AGCAGCCCAGAAGCC | 25807 |
rs56246552 | in-del | -/TTTTT | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262155 | TTTTTTTTTTTTTTT[-/TTTTT]GGAGAGAGTCTTGCT | 25807 |
rs57983344 | snp | C/G | 0.0360663 | 0.129354 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266247 | TCCTTACTGGCACAG[C/G]CCCTCTGGCCCTGGC | 25807 |
rs58112306 | in-del | -/A | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262833 | GTCTCAGTCTCCCAA[-/A]GTAGCTGGGACTACA | 25807 |
rs59054440 | snp | G/T | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263273 | TAGTCTCGAACTCCT[G/T]ACCTCGTGATCCGCC | 25807 |
rs59740128 | snp | C/T | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29261567 | TCGCCACACTCCAGC[C/T]TGGGTGACAGAATGA | 25807 |
rs60160467 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263294 | GTGATCCGCCCACCT[G/T]GGCCTCCCAAAGTGT | 25807 |
rs62226082 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266424 | AATTCTTTTCCTCAG[A/G]GTATGATGAAATAAA | 25807 |
rs73401085 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29261165 | GGTCTGTAACTCAAG[A/G]CCCACCCGTCCTGGA | 25807 |
rs73401086 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29261238 | TGGATAACTCCTGTC[A/C]CCAATCCAGAGTGCA | 25807 |
rs73401088 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RHBDD3 | GRCh38.p7 | 22:29265815 | GCCTTAGTGGAGCTC[A/C]GACCCTAACCCATGC | 25807 |
rs73884707 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263734 | TGTGCACGGCTCCTT[C/G]GTATTGCTTGGGCCT | 25807 |
rs73884709 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268419 | GGGTCGTTCGTCTCT[A/G]GGCTTGGCTGGGAAG | 25807 |
rs75890789 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, synonymous-codon | RHBDD3 | GRCh38.p7 | 22:29264364 | GTCTTCCCACAGCCA[A/G]CACTTAATCATTGGT | 25807 |
rs75906006 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29261998 | TTTCCTCATTGAATC[A/G]ACTTGGCACTCTTGT | 25807 |
rs76174678 | snp | C/T | | | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268988 | ACAGAATGTGCTTCC[C/T]TCCTCCAGGGCCCCC | 25807 |
rs76776803 | snp | A/G | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262552 | TCCATATTATTTTTA[A/G]GACCAGCTTGCTAAT | 25807 |
rs77078685 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266872 | TGCATTGTCCTTCCC[C/T]CCATTTTGCCAGCAG | 25807 |
rs77107431 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29270021 | TGGTCCTTAGTTTCC[C/T]TTCCTGTAAAATACA | 25807 |
rs78338750 | snp | A/G | 0.0517044 | 0.152246 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267210 | AGGTCCAGGAAGGTG[A/G]GCAGGGTCAGCCTTG | 25807 |
rs78465643 | snp | C/G | 0.000526604 | 0.016218 | missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29265529 | ACCAGGCCGGGGCCG[C/G]CCCCCACCAGCCACA | 25807 |
rs111527234 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29269211 | TAGGAGGAACAAAAG[A/G]CCGAGCCTTCATTTG | 25807 |
rs111585451 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263406 | CTGGTCTTGAACTCC[A/G/T]GACCTCAAGTGATCT | 25807 |
rs111808326 | snp | A/C | 0.5 | 0 | downstream-variant-500B | EMID1, RHBDD3 | GRCh38.p7 | 22:29259701 | TGCTGGAGGACAGAG[A/C]CTCCTGGAGGTATAG | 25807 |
rs111892587 | snp | A/C/T | 0.00135627 | 0.0260063 | utr-variant-5-prime, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268292 | CGCCTAGAGGGAAAG[A/C/T]GAGAGGGAGACGGAC | 25807 |
rs112004180 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266651 | CTTCTCCCCCGTGCT[C/G]TTCTCTTGCATCCAG | 25807 |
rs112102989 | snp | A/C | 0.5 | 0 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29260695 | GCATCCCCCCCATCA[A/C]CCTCACCTCACTCCG | 25807 |
rs112247936 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267844 | GAGAACCCTGAATCC[A/C]TTCCGCGCACACCCG | 25807 |
rs112252047 | in-del | -/TTAT | 0.5 | 0 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29261653 | GTGCTCTAGCACGAC[-/TTAT]TTATTTATTTATTTT | 25807 |
rs112304926 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RHBDD3 | GRCh38.p7 | 22:29265722 | GCTTTTATCTCACCA[A/G]TACCCTCTCAAGCAC | 25807 |
rs112551464 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267034 | TCATGGCTCCTCTGA[G/T]CCAACCCCACATTCC | 25807 |
rs112726426 | snp | A/C | 0 | 0 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29260066 | CTGCCTGGGCTAGGG[A/C]GGCCCAGGACCCTCG | 25807 |
rs112850193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262390 | GTGATCTGTCTGCCT[C/T]GGCCTCTCAAAGTGC | 25807 |
rs112988085 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, missense | RHBDD3 | GRCh38.p7 | 22:29264301 | CAGGTTGAAGGTTAC[C/G]CTACACCAGGGCCAC | 25807 |
rs113274927 | snp | A/G | 0.0391387 | 0.134304 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268065 | GCTGAGAGCCTCTCC[A/G]GTTTCACGCTGAGAC | 25807 |
rs113362509 | snp | C/T | 5.03816e-05 | 0.00501879 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260176 | CCTCCACACGGCCTG[C/T]GGCTGCCAGTGCCAC | 25807 |
rs113452614 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29264846 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT | 25807 |
rs113663816 | snp | C/T | 0.444444 | 0.157135 | intron-variant, missense | RHBDD3 | GRCh38.p7 | 22:29264272 | CCCAACATCCAAGGC[C/T]GTCCCAGGTGTGCCA | 25807 |
rs113911633 | snp | C/T | 0.0810805 | 0.184299 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266253 | CTGGCACAGCCCCTC[C/T]GGCCCTGGCTCCCCT | 25807 |
rs114250658 | snp | A/T | 0.00795532 | 0.062565 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267522 | ATCTGTCTGGTTCGA[A/T]CTCAGCTGGTGACTT | 25807 |
rs114640172 | snp | A/C/T | 0.00810788 | 0.0631539 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260708 | CACCCTCACCTCACT[A/C/T]CGGCAGGATGGGTGA | 25807 |
rs114806687 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29269915 | TACCATGTGCTGTAC[C/T]GTATTAGAATTACAG | 25807 |
rs114897109 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262023 | TCTTGTCAAAATAAA[C/T]TGACTATACAGTAAA | 25807 |
rs115286357 | snp | A/G | 0.00702353 | 0.0588425 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29260251 | GCCTGTTGGGGGTGG[A/G]GGGAGAAGTGGGGAG | 25807 |
rs116644628 | snp | A/G | 0.00408328 | 0.0449996 | synonymous-codon, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263857 | GCCGGCAAGGAGGCC[A/G]CAAAGGAGCTGCAGG | 25807 |
rs116729446 | snp | A/G | 0.0189856 | 0.0955633 | utr-variant-5-prime, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268132 | TGGCCCGAGTGTCAC[A/G]TCGGGCGCTCTTTAG | 25807 |
rs117474693 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29266355 | TCTTTTTACAGATGA[A/G]CCTCATTTTACAGAT | 25807 |
rs117950019 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29270185 | AGTGACTGCTCTAAA[A/G]TGTTAAACCGTTGCC | 25807 |
rs118049515 | snp | A/G | 0.000354296 | 0.013305 | synonymous-codon, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263962 | ACGGGGCCGTCTAGG[A/G]CGGTGTCCCTCCCCA | 25807 |
rs138506952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29261006 | CCAGCATGGAATAGC[A/G]TCACCCTGGTCAGCA | 25807 |
rs138725360 | snp | C/T | 0.00375894 | 0.0431896 | synonymous-codon, intron-variant | RHBDD3 | GRCh38.p7 | 22:29264007 | GTGGACAGGCATGTA[C/T]CCACAGCTGCCGGCT | 25807 |
rs138870856 | snp | C/T | 0.0216527 | 0.101772 | stop-gained, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260442 | CTCATCCAAGGCCGC[C/T]CACATCGGAGTCCCT | 25807 |
rs139372280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29261451 | TTTTTAAAATTAGCT[A/G]GACGTGGCAGTGCAC | 25807 |
rs139677866 | snp | A/C | 5.61593e-05 | 0.00529872 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260585 | AGAGGTCAGGGGAGG[A/C]CACATAAGGCGGTCC | 25807 |
rs139842640 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268036 | CGGAACCATTCCAAA[C/T]AGCCTAGTCTCGTGC | 25807 |
rs139864944 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RHBDD3 | GRCh38.p7 | 22:29263180 | CTCCTAAGTAGCTGG[A/G]ATTACAGGTGCACGC | 25807 |
rs139903286 | snp | C/T | | | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29268862 | GTGCCGGCCTATGAG[C/T]GGGAGCCCCGTCATC | 25807 |
rs140310182 | in-del | -/C | | | intron-variant | RHBDD3 | GRCh38.p7 | 22:29262139 | TATAATTTTGTACGG[-/C]TTTTTTTTTTTTTTT | 25807 |
rs140437469 | snp | A/G | 3.40223e-05 | 0.00412432 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260720 | ACTCCGGCAGGATGG[A/G]TGACAGGCAGCTCCG | 25807 |
rs140704715 | snp | A/G | 0.000236686 | 0.010876 | missense, intron-variant | RHBDD3 | GRCh38.p7 | 22:29263949 | GTGGCAGTGCCCCAC[A/G]GGGCCGTCTAGGGCG | 25807 |
rs140828017 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29269960 | GACACAAAGTAAACA[C/G]ATTAGGCCTGGCTGG | 25807 |
rs141666277 | snp | A/G | 0.0284887 | 0.1159 | intron-variant, missense | RHBDD3 | GRCh38.p7 | 22:29260916 | CCAAAAGCAGCCAGG[A/G]GTGGGCCCACGCCAC | 25807 |
rs141988655 | snp | C/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | EWSR1, RHBDD3 | GRCh38.p7 | 22:29267320 | TGGGCACCTTAGCAA[C/G]GGTGAAGGGCTTACC | 25807 |
rs142277035 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, intron-variant | EMID1, RHBDD3 | GRCh38.p7 | 22:29259468 | CTCTGAGCCCCCAGG[A/C]CCTCCCGCATCTCAG | 25807 |
rs142287656 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | RHBDD3 | GRCh38.p7 | 22:29261072 | GCTACTCAGCCAAAC[A/C]GAGCCAGGTATGCCT | 25807 |
rs142462633 | snp | G/T | 0.00165191 | 0.0286919 | missense, nc-transcript-variant | RHBDD3 | GRCh38.p7 | 22:29260848 | GGGTTCCAGCCACCG[G/T]AAGGCCCCAGCTGCA | 25807 |
rs142646759 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | EWSR1, RHBDD3 | GRCh38.p7 | 22:29269854 | TTTGCGTGGCTGGAC[A/G]TGCCTTTTTTCAGTC | 25807 |