ClinVar Miner

List of variants in gene combination EPCAM, MSH2 reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000251.2(MSH2):c.(?-1)_(1276+1_1277-1)del
NM_002354.2(EPCAM):c.(903+1_904-1)_(*1_?)del

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