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rs397508862(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs397508862
GeneBRCA1
Chromosome17
Position43,094,157
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;C) 6 BRCA1 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar