List of variants in gene combination BRCA1, LOC126862571 reported as benign for Breast and/or ovarian 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: 4

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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.4039A>G (p.Arg1347Gly)	rs28897689	0.00419
NM_007294.4(BRCA1):c.3748G>A (p.Glu1250Lys)	rs28897686	0.00017
NM_007294.4(BRCA1):c.3600G>C (p.Gln1200His)	rs56214134

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