List of variants in gene RAD51 reported as pathogenic for carcinoma

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002875.5(RAD51):c.449G>A (p.Arg150Gln)	rs121917739	0.00171
NM_002875.5(RAD51):c.760C>T (p.Arg254Ter)	rs199925463

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