RHBDD3
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs8550snpA/G0.2810490.248064utr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259382ACCTCGGGGTGGGGA[A/G]CCCAGCACTGGACAA25807
rs9537snpA/G0.4605890.13473utr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259427AGGCAAGAAGCCCCC[A/G]GTGATCCAGTCAGAG25807
rs710196snpC/T00utr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259455CCTCAGTTCTTCCCT[C/T]TGAGCCCCCAGGCCC25807
rs710197snpC/T00utr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259448CTTCTTGCCTCAGTT[C/T]TTCCCTCTGAGCCCC25807
rs879580snpA/G0.392670.205293synonymous-codon, intron-variantRHBDD3GRCh38.p722:29263971CATGCTGGCTGGGGA[A/G]GGACACCGCCCTAGA25807
rs2231392snpC/T0.0003635220.013477utr-variant-5-prime, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268334CCGTGGACGCCATTT[C/T]CTCTCCTTCCTCCTC25807
rs2231393snpA/Gmissense, intron-variantRHBDD3GRCh38.p722:29264078GCCTCAGCCCTGCTC[A/G]CCCTGGCTTCTGGGC25807
rs2231394snpC/T0.004712510.048312missense, intron-variantRHBDD3GRCh38.p722:29263964GCTGGGGAGGGACAC[C/T]GCCCTAGACGGCCCC25807
rs2231395snpA/G0.03989480.135484intron-variantRHBDD3GRCh38.p722:29263808CTGAGCCCAGGGCCC[A/G]TGGGGATGTGTGGGT25807
rs2231396snpC/T0.04639470.145069intron-variantRHBDD3GRCh38.p722:29263726GCAATACCAAGGAGC[C/T]GTGCACACACATTCC25807
rs2231397snpA/G0.004205510.0456625missense, nc-transcript-variantRHBDD3GRCh38.p722:29260717AGCTGCCTGTCACCC[A/G]TCCTGCCGGAGTGAG25807
rs2231398snpA/C0.4106590.191543synonymous-codon, nc-transcript-variantRHBDD3GRCh38.p722:29260400GGAGGGCATCCAGGC[A/C]TCGCTTCTTGACGGG25807
rs2231399snpC/T0.004416430.0467837synonymous-codon, nc-transcript-variantRHBDD3GRCh38.p722:29260156CCGTGTGGAGGGTGC[C/T]GTGTCACTGTTGGTT25807
rs2272902snpA/G0.0006477940.0179855missense, intron-variantRHBDD3GRCh38.p722:29264110TGCAGGAATCTCAGC[A/G]TGCCCAGGTGGCACT25807
rs2301290snpA/G0.3297830.236927intron-variant, upstream-variant-2KBRHBDD3GRCh38.p722:29265352CCTGTCTAAGGCCAT[A/G]CTTTCCCGGGACACT25807
rs2301291snpA/G0.4863320.08153intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268434GGGCTTGGCTGGGAA[A/G]ACTGAGTGGAGTTGC25807
rs2857460snpC/T0.2075590.246371intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268917TCTGGCGCTGCCGAG[C/T]TGCCCCCTCTGTGGC25807
rs2857466snpC/T0.4873050.0786545intron-variantRHBDD3GRCh38.p722:29261615ttaaaaaaaaaaTCT[C/T]AGAAGCAGAACACCA25807
rs3204856snpA/Gutr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259542CAAATGCTTGTGACA[A/G]ATGCCAGGAGGTAGA25807
rs4505624snpC/T0.08071490.183963intron-variantRHBDD3GRCh38.p722:29262745gaagtctcgctctct[C/T]gcccaggctggagtg25807
rs5763119snpA/G00intron-variantRHBDD3GRCh38.p722:29262738ttgagaggaagtctc[A/G]ctctctcgcccaggc25807
rs5763120snpG/T0.0003992810.0141238missense, intron-variantRHBDD3GRCh38.p722:29263889AGGGTGGCTCAGAGC[G/T]GAGCAGTGGGGTCAG25807
rs9613850snpC/G00missense, intron-variantRHBDD3GRCh38.p722:29263885AGGAAGGGTGGCTCA[C/G]AGCTGAGCAGTGGGG25807
rs11539373snpC/T0.02172360.101931upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variantEWSR1, RHBDD3GRCh38.p722:29267762GCCTTTCGGGGTTGC[C/T]GGGCGCGCTCTGCAG25807
rs11703074snpG/T00intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29270009acataagtaatctgg[G/T]ccttagtttcctttc25807
rs11912931snpC/G0.05132620.151752intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500BEMID1, RHBDD3GRCh38.p722:29259864TGCTGCCTCCAAGGA[C/G]GTCCAGGTTGAAAAA25807
rs13058014snpC/Gintron-variantRHBDD3GRCh38.p722:29260283GTCAGGGCCACCCCG[C/G]CCCCTATACCAGGGG25807
rs16987345snpA/G0.02172360.101931utr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259506ATGGGGACATGGAGA[A/G]GAAGGGGCCGCCTAC25807
rs34091309snpA/C0.04601420.144533intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268888TCATCCTTAAGACCC[A/C]GTCGGCTGGGGCGTC25807
rs34614149in-del-/T0.4795020.0991411intron-variantRHBDD3GRCh38.p722:29262140ATAATTTTGTACGGC[-/T]TTTTTTTTTTTTTTT25807
rs35098478in-del-/Tintron-variantRHBDD3GRCh38.p722:29262143AATTTTGTACGGCTT[-/T]TTTTTTTTTTTTTTT25807
rs35125319in-del-/C0.0001884270.00970453intron-variantRHBDD3GRCh38.p722:29260683CACCTGGACTGGCAT[-/C]CCCCCCCATCACCCT25807
rs35726449in-del-/Cframeshift-variant, nc-transcript-variantRHBDD3GRCh38.p722:29260761CGGGGTGGCAAGGAG[-/C]CTCAGGGGCCAGCAC25807
rs35850999in-del-/Aframeshift-variant, intron-variantRHBDD3GRCh38.p722:29264058GCCAGCAGCACTGCC[-/A]AGCAGCCCAGAAGCC25807
rs56246552in-del-/TTTTTintron-variantRHBDD3GRCh38.p722:29262155TTTTTTTTTTTTTTT[-/TTTTT]GGAGAGAGTCTTGCT25807
rs57983344snpC/G0.03606630.129354upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266247TCCTTACTGGCACAG[C/G]CCCTCTGGCCCTGGC25807
rs58112306in-del-/Aintron-variantRHBDD3GRCh38.p722:29262833GTCTCAGTCTCCCAA[-/A]GTAGCTGGGACTACA25807
rs59054440snpG/Tintron-variantRHBDD3GRCh38.p722:29263273TAGTCTCGAACTCCT[G/T]ACCTCGTGATCCGCC25807
rs59740128snpC/Tintron-variantRHBDD3GRCh38.p722:29261567TCGCCACACTCCAGC[C/T]TGGGTGACAGAATGA25807
rs60160467snpG/T0.01387990.0821421intron-variantRHBDD3GRCh38.p722:29263294GTGATCCGCCCACCT[G/T]GGCCTCCCAAAGTGT25807
rs62226082snpA/G0.01151440.0749975upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266424AATTCTTTTCCTCAG[A/G]GTATGATGAAATAAA25807
rs73401085snpA/G0.01506060.0854603intron-variant, utr-variant-5-primeRHBDD3GRCh38.p722:29261165GGTCTGTAACTCAAG[A/G]CCCACCCGTCCTGGA25807
rs73401086snpA/C0.01506060.0854603intron-variant, nc-transcript-variant, utr-variant-5-primeRHBDD3GRCh38.p722:29261238TGGATAACTCCTGTC[A/C]CCAATCCAGAGTGCA25807
rs73401088snpA/C0.007559070.0610114intron-variant, upstream-variant-2KBRHBDD3GRCh38.p722:29265815GCCTTAGTGGAGCTC[A/C]GACCCTAACCCATGC25807
rs73884707snpC/G0.01663250.0896639intron-variantRHBDD3GRCh38.p722:29263734TGTGCACGGCTCCTT[C/G]GTATTGCTTGGGCCT25807
rs73884709snpA/G0.02678780.112589intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268419GGGTCGTTCGTCTCT[A/G]GGCTTGGCTGGGAAG25807
rs75890789snpA/G0.02250450.103662intron-variant, synonymous-codonRHBDD3GRCh38.p722:29264364GTCTTCCCACAGCCA[A/G]CACTTAATCATTGGT25807
rs75906006snpA/G0.03683530.130617intron-variantRHBDD3GRCh38.p722:29261998TTTCCTCATTGAATC[A/G]ACTTGGCACTCTTGT25807
rs76174678snpC/Tintron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268988ACAGAATGTGCTTCC[C/T]TCCTCCAGGGCCCCC25807
rs76776803snpA/Gintron-variantRHBDD3GRCh38.p722:29262552TCCATATTATTTTTA[A/G]GACCAGCTTGCTAAT25807
rs77078685snpC/T0.0003992810.0141238upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266872TGCATTGTCCTTCCC[C/T]CCATTTTGCCAGCAG25807
rs77107431snpC/T0.01859380.0946107intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29270021TGGTCCTTAGTTTCC[C/T]TTCCTGTAAAATACA25807
rs78338750snpA/G0.05170440.152246upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29267210AGGTCCAGGAAGGTG[A/G]GCAGGGTCAGCCTTG25807
rs78465643snpC/G0.0005266040.016218missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-primeRHBDD3GRCh38.p722:29265529ACCAGGCCGGGGCCG[C/G]CCCCCACCAGCCACA25807
rs111527234snpA/G0.50intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29269211TAGGAGGAACAAAAG[A/G]CCGAGCCTTCATTTG25807
rs111585451snpA/G/T0.0003992810.0141238intron-variantRHBDD3GRCh38.p722:29263406CTGGTCTTGAACTCC[A/G/T]GACCTCAAGTGATCT25807
rs111808326snpA/C0.50downstream-variant-500BEMID1, RHBDD3GRCh38.p722:29259701TGCTGGAGGACAGAG[A/C]CTCCTGGAGGTATAG25807
rs111892587snpA/C/T0.001356270.0260063utr-variant-5-prime, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268292CGCCTAGAGGGAAAG[A/C/T]GAGAGGGAGACGGAC25807
rs112004180snpC/G0.001197370.0244387upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266651CTTCTCCCCCGTGCT[C/G]TTCTCTTGCATCCAG25807
rs112102989snpA/C0.50intron-variantRHBDD3GRCh38.p722:29260695GCATCCCCCCCATCA[A/C]CCTCACCTCACTCCG25807
rs112247936snpA/Cupstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variantEWSR1, RHBDD3GRCh38.p722:29267844GAGAACCCTGAATCC[A/C]TTCCGCGCACACCCG25807
rs112252047in-del-/TTAT0.50intron-variantRHBDD3GRCh38.p722:29261653GTGCTCTAGCACGAC[-/TTAT]TTATTTATTTATTTT25807
rs112304926snpA/G0.50intron-variant, upstream-variant-2KBRHBDD3GRCh38.p722:29265722GCTTTTATCTCACCA[A/G]TACCCTCTCAAGCAC25807
rs112551464snpG/T00upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29267034TCATGGCTCCTCTGA[G/T]CCAACCCCACATTCC25807
rs112726426snpA/C00downstream-variant-500B, synonymous-codon, nc-transcript-variantEMID1, RHBDD3GRCh38.p722:29260066CTGCCTGGGCTAGGG[A/C]GGCCCAGGACCCTCG25807
rs112850193snpC/T0.0003992810.0141238intron-variantRHBDD3GRCh38.p722:29262390GTGATCTGTCTGCCT[C/T]GGCCTCTCAAAGTGC25807
rs112988085snpC/G0.001596170.0282053intron-variant, missenseRHBDD3GRCh38.p722:29264301CAGGTTGAAGGTTAC[C/G]CTACACCAGGGCCAC25807
rs113274927snpA/G0.03913870.134304utr-variant-5-prime, intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268065GCTGAGAGCCTCTCC[A/G]GTTTCACGCTGAGAC25807
rs113362509snpC/T5.03816e-050.00501879missense, nc-transcript-variantRHBDD3GRCh38.p722:29260176CCTCCACACGGCCTG[C/T]GGCTGCCAGTGCCAC25807
rs113452614snpC/T00intron-variant, utr-variant-5-primeRHBDD3GRCh38.p722:29264846GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGCT25807
rs113663816snpC/T0.4444440.157135intron-variant, missenseRHBDD3GRCh38.p722:29264272CCCAACATCCAAGGC[C/T]GTCCCAGGTGTGCCA25807
rs113911633snpC/T0.08108050.184299upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266253CTGGCACAGCCCCTC[C/T]GGCCCTGGCTCCCCT25807
rs114250658snpA/T0.007955320.062565upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variantEWSR1, RHBDD3GRCh38.p722:29267522ATCTGTCTGGTTCGA[A/T]CTCAGCTGGTGACTT25807
rs114640172snpA/C/T0.008107880.0631539missense, nc-transcript-variantRHBDD3GRCh38.p722:29260708CACCCTCACCTCACT[A/C/T]CGGCAGGATGGGTGA25807
rs114806687snpC/T0.01976870.0974348intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29269915TACCATGTGCTGTAC[C/T]GTATTAGAATTACAG25807
rs114897109snpC/T0.01032950.0711199intron-variantRHBDD3GRCh38.p722:29262023TCTTGTCAAAATAAA[C/T]TGACTATACAGTAAA25807
rs115286357snpA/G0.007023530.0588425intron-variantRHBDD3GRCh38.p722:29260251GCCTGTTGGGGGTGG[A/G]GGGAGAAGTGGGGAG25807
rs116644628snpA/G0.004083280.0449996synonymous-codon, intron-variantRHBDD3GRCh38.p722:29263857GCCGGCAAGGAGGCC[A/G]CAAAGGAGCTGCAGG25807
rs116729446snpA/G0.01898560.0955633utr-variant-5-prime, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268132TGGCCCGAGTGTCAC[A/G]TCGGGCGCTCTTTAG25807
rs117474693snpA/G0.007559070.0610114upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29266355TCTTTTTACAGATGA[A/G]CCTCATTTTACAGAT25807
rs117950019snpA/G0.01387990.0821421intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29270185AGTGACTGCTCTAAA[A/G]TGTTAAACCGTTGCC25807
rs118049515snpA/G0.0003542960.013305synonymous-codon, intron-variantRHBDD3GRCh38.p722:29263962ACGGGGCCGTCTAGG[A/G]CGGTGTCCCTCCCCA25807
rs138506952snpA/G0.0007984030.0199641intron-variant, utr-variant-5-primeRHBDD3GRCh38.p722:29261006CCAGCATGGAATAGC[A/G]TCACCCTGGTCAGCA25807
rs138725360snpC/T0.003758940.0431896synonymous-codon, intron-variantRHBDD3GRCh38.p722:29264007GTGGACAGGCATGTA[C/T]CCACAGCTGCCGGCT25807
rs138870856snpC/T0.02165270.101772stop-gained, nc-transcript-variantRHBDD3GRCh38.p722:29260442CTCATCCAAGGCCGC[C/T]CACATCGGAGTCCCT25807
rs139372280snpA/G0.0003992810.0141238intron-variantRHBDD3GRCh38.p722:29261451TTTTTAAAATTAGCT[A/G]GACGTGGCAGTGCAC25807
rs139677866snpA/C5.61593e-050.00529872missense, nc-transcript-variantRHBDD3GRCh38.p722:29260585AGAGGTCAGGGGAGG[A/C]CACATAAGGCGGTCC25807
rs139842640snpC/T0.0003992810.0141238utr-variant-5-prime, intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268036CGGAACCATTCCAAA[C/T]AGCCTAGTCTCGTGC25807
rs139864944snpA/G0.02172360.101931intron-variantRHBDD3GRCh38.p722:29263180CTCCTAAGTAGCTGG[A/G]ATTACAGGTGCACGC25807
rs139903286snpC/Tintron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29268862GTGCCGGCCTATGAG[C/T]GGGAGCCCCGTCATC25807
rs140310182in-del-/Cintron-variantRHBDD3GRCh38.p722:29262139TATAATTTTGTACGG[-/C]TTTTTTTTTTTTTTT25807
rs140437469snpA/G3.40223e-050.00412432missense, nc-transcript-variantRHBDD3GRCh38.p722:29260720ACTCCGGCAGGATGG[A/G]TGACAGGCAGCTCCG25807
rs140704715snpA/G0.0002366860.010876missense, intron-variantRHBDD3GRCh38.p722:29263949GTGGCAGTGCCCCAC[A/G]GGGCCGTCTAGGGCG25807
rs140828017snpC/G0.006766090.0577691intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29269960GACACAAAGTAAACA[C/G]ATTAGGCCTGGCTGG25807
rs141666277snpA/G0.02848870.1159intron-variant, missenseRHBDD3GRCh38.p722:29260916CCAAAAGCAGCCAGG[A/G]GTGGGCCCACGCCAC25807
rs141988655snpC/G0.01032950.0711199upstream-variant-2KB, intron-variantEWSR1, RHBDD3GRCh38.p722:29267320TGGGCACCTTAGCAA[C/G]GGTGAAGGGCTTACC25807
rs142277035snpA/Cutr-variant-3-prime, downstream-variant-500B, intron-variantEMID1, RHBDD3GRCh38.p722:29259468CTCTGAGCCCCCAGG[A/C]CCTCCCGCATCTCAG25807
rs142287656snpA/C0.005178220.0506191intron-variant, utr-variant-5-primeRHBDD3GRCh38.p722:29261072GCTACTCAGCCAAAC[A/C]GAGCCAGGTATGCCT25807
rs142462633snpG/T0.001651910.0286919missense, nc-transcript-variantRHBDD3GRCh38.p722:29260848GGGTTCCAGCCACCG[G/T]AAGGCCCCAGCTGCA25807
rs142646759snpA/G0.003189780.0398085intron-variant, upstream-variant-2KBEWSR1, RHBDD3GRCh38.p722:29269854TTTGCGTGGCTGGAC[A/G]TGCCTTTTTTCAGTC25807
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