List of variants in gene combination BRCA1, LOC126862571 reported as uncertain significance for Breast and/or ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3515A>G (p.Glu1172Gly)	rs80357206	0.00006
NM_007294.4(BRCA1):c.3758C>G (p.Ser1253Cys)	rs397509100	0.00004
NM_007294.4(BRCA1):c.3711A>G (p.Ile1237Met)	rs80357388	0.00001
NM_007294.4(BRCA1):c.3308G>A (p.Cys1103Tyr)	rs80357135
NM_007294.4(BRCA1):c.3437G>C (p.Cys1146Ser)	rs80357247
NM_007294.4(BRCA1):c.3809G>A (p.Cys1270Tyr)	rs1207787135
NM_007294.4(BRCA1):c.3852C>A (p.His1284Gln)	rs776070899
NM_007294.4(BRCA1):c.4060AAT[1] (p.Asn1355del)	rs80358341

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