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rs80357212(A;G)

From SNPedia

BRCA1 variant of unclear significance
Is agenotype
ofrs80357212
GeneBRCA1
Chromosome17
Position43,047,643
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 BRCA1 variant of unclear significance
(G;G) 0 common in clinvar

see discussion at rs80357212