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rs397507815(CT;CT)

From SNPedia
common in clinvar
Is agenotype
ofrs397507815
GeneBRCA2
Chromosome13
Position32,340,309
Merged intoRs80359551
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CT) 6 BRCA2 variant considered pathogenic for breast cancer
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar