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rs397507789(AAAAG;AAAAG)

From SNPedia
common in clinvar
Is agenotype
ofrs397507789
GeneBRCA2
Chromosome13
Position32,339,935
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;AAAAG) 6 Miscall in 23andMe v4 data; otherwise, BRCA2 variant considered pathogenic for breast cancer
(AAAAG;AAAAG) 0 common in clinvar