ClinVar Miner

List of variants reported as likely pathogenic for Breast carcinoma by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.650G>A (p.Arg217His)	rs140342925	0.00009
NM_007194.4(CHEK2):c.342G>A (p.Trp114Ter)	rs756949505	0.00001

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