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rs397508981(CTCAG;CTCAG)

From SNPedia

common in clinvar
Is agenotype
ofrs397508981
GeneBRCA1
Chromosome17
Position43,092,966
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CTCAG) 6 BRCA1 variant considered pathogenic for breast cancer
(CTCAG;CTCAG) 0 common in clinvar