List of variants in gene combination BRCA1, LOC126862571 reported as pathogenic for Breast 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3626dup (p.Leu1209fs)	rs80357571
NM_007294.4(BRCA1):c.3770_3771del (p.Glu1257fs)	rs80357579
NM_007294.4(BRCA1):c.3794del (p.Asn1265fs)	rs80357767
NM_007294.4(BRCA1):c.4062_4066del (p.Asn1354fs)	rs886040192

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