List of variants in gene combination BRCA1, LOC126862571 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_007294.4(BRCA1):c.3418A>G (p.Ser1140Gly)	rs2227945	0.01054
NM_007294.4(BRCA1):c.3708T>G (p.Asn1236Lys)	rs28897687	0.00031

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