List of variants in gene combination BRCA1, LOC126862571 reported as benign for anemia

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.3548A>G (p.Lys1183Arg)	rs16942	0.30784
NM_007294.4(BRCA1):c.3296C>T (p.Pro1099Leu)	rs80357201	0.00016

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