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rs886038129(CTCT;CTCT)

From SNPedia
common in clinvar
Is agenotype
ofrs886038129
GeneBRCA2
Chromosome13
Position32,340,075
Merged intoRs276174862
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CTCT) 6 BRCA2 variant considered pathogenic for breast cancer
(CTCT;CTCT) 0 common in clinvar