ClinVar Miner

List of variants in gene RPS7 studied for not provided

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001011.4(RPS7):c.357-52G>C rs7576238 0.83566
NM_001011.4(RPS7):c.147+62A>G rs3087873 0.77182
NM_001011.4(RPS7):c.292-233T>C rs9808074 0.21982
NM_001011.4(RPS7):c.292-121C>T rs72767177 0.21593
NM_001011.4(RPS7):c.508-12C>A rs2071639 0.12923
NM_001011.4(RPS7):c.292-262G>T rs75452965 0.09045
NM_001011.4(RPS7):c.148-194C>T rs62106032 0.06747
NM_001011.4(RPS7):c.291+83G>A rs80103345 0.05422
NM_001011.4(RPS7):c.292-153G>C rs62106037 0.05419
NM_001011.4(RPS7):c.-47G>T rs11558965 0.05356
NM_001011.4(RPS7):c.148-138T>C rs62106033 0.05249
NM_001011.4(RPS7):c.356+65A>G rs73137100 0.04530
NM_001011.4(RPS7):c.508-197C>T rs59060135 0.04202
NM_001011.4(RPS7):c.147+77G>C rs59077127 0.04057
NM_001011.4(RPS7):c.292-39C>T rs73910594 0.03067
NC_000002.12:g.3581089G>A rs11691831 0.02028
NM_001011.4(RPS7):c.147+63G>A rs11683831 0.01796
NM_001011.4(RPS7):c.147+142T>A rs113260758 0.01725
NM_001011.4(RPS7):c.356+29G>A rs113127192 0.01678
NM_001011.4(RPS7):c.356+89T>C rs140005491 0.00717
NC_000002.12:g.3580993G>C rs112774737 0.00564
NM_001011.4(RPS7):c.507+77C>T rs145852027 0.00470
NM_001011.4(RPS7):c.292-21A>G rs150686417 0.00436
NC_000002.12:g.3575072G>T rs115090628 0.00123
NM_001011.4(RPS7):c.66C>T (p.Gly22=) rs773617808 0.00001
NM_001011.4(RPS7):c.77C>T (p.Ala26Val) rs939123022 0.00001
NM_001011.4(RPS7):c.-19+1G>C rs1064796859
NM_001011.4(RPS7):c.11C>T (p.Ser4Leu) rs781456307
NM_001011.4(RPS7):c.148-26C>A rs62106034
NM_001011.4(RPS7):c.291+2dup rs745508670
NM_001011.4(RPS7):c.292-125T>C rs72767176
NM_001011.4(RPS7):c.329C>G (p.Thr110Arg) rs2528181238
NM_001011.4(RPS7):c.357-3dup rs140914434
NM_001011.4(RPS7):c.528C>T (p.Val176=) rs1572360965
NM_001011.4(RPS7):c.76-3T>G rs1364756725

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