ClinVar Miner

List of variants reported as likely pathogenic for Neoplasm of stomach by CSER _CC_NCGL, University of Washington

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_004360.5(CDH1):c.2494G>A (p.Val832Met)	rs35572355	0.00004

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