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rs80356860(C;G)

From SNPedia

BRCA1 variant of unclear significance
Is agenotype
ofrs80356860
GeneBRCA1
Chromosome17
Position43,063,909
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;G) 3 BRCA1 variant of unclear significance
(G;G) 0 common in clinvar