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rs397509007(CT;CT)

From SNPedia
common in clinvar
Is agenotype
ofrs397509007
GeneBRCA1
Chromosome17
Position43,092,786
Merged intoRs80357540
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CT) 6 BRCA1 variant considered pathogenic for breast cancer
(CT;CT) 0 common in clinvar