List of variants in gene PPM1D reported as likely benign for breast cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003620.4(PPM1D):c.1149A>C (p.Gly383=)	rs111239559	0.00849
NM_003620.4(PPM1D):c.456C>T (p.Ala152=)	rs149400522	0.00475
NM_003620.4(PPM1D):c.1017+51A>G	rs144142345	0.00301

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