List of variants in gene combination BRCA2, LOC106721785 reported as likely benign for DNA repair disease

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_000059.4(BRCA2):c.-175C>T	rs55880202	0.00642
NM_000059.4(BRCA2):c.-59_-57del	rs545321666

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