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rs397507812(-;-)

From SNPedia
common in clinvar
Is agenotype
ofrs397507812
GeneBRCA2
Chromosome13
Position32,340,300
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 0 common in clinvar
(-;G) 6 Possible miscall in Ancestry v2c data; otherwise, BRCA2 variant considered pathogenic for breast cancer