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rs397507869(T;T)

From SNPedia
(Redirected from Rs397507869(CT;CT))
common in clinvar
Is agenotype
ofrs397507869
GeneBRCA2
Chromosome13
Position32,340,956
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;T) 6 Likely miscall in Ancestry v2c data; otherwise, BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar