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rs397507791(CA;CA)

From SNPedia
common in clinvar
Is agenotype
ofrs397507791
GeneBRCA2
Chromosome13
Position32,339,947
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CA) 6 BRCA2 variant considered pathogenic for breast cancer
(AC;AC) 0 common in clinvar
(CA;CA) 0 common in clinvar