ClinVar Miner

List of variants reported as uncertain significance for Hereditary cancer-predisposing syndrome by GeneID Lab - Advanced Molecular Diagnostics

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_002485.5(NBN):c.511A>G (p.Ile171Val) rs61754966 0.00145
NM_002485.5(NBN):c.1262T>C (p.Leu421Ser) rs104895032 0.00027
NM_001048174.2(MUTYH):c.563G>A (p.Gly188Glu) rs768553551 0.00001
NM_032043.3(BRIP1):c.2524C>T (p.Leu842Phe) rs786201802

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