ClinVar Miner

List of variants reported as benign for not specified by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.7397= (p.Val2466=) rs169547 0.02098
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr) rs4986854 0.00098
NM_007294.4(BRCA1):c.981A>G (p.Thr327=) rs1800063 0.00065
NM_007294.4(BRCA1):c.1911T>C (p.Thr637=) rs62625305 0.00013

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