ClinVar Miner

Variants in gene BRCA1 with conflicting interpretations "likely benign" and "likely benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys) rs41286300
NM_007294.4(BRCA1):c.3296C>T (p.Pro1099Leu) rs80357201
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr) rs4986854

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