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rs786203399(TT;TT)

From SNPedia

common in clinvar
Is agenotype
ofrs786203399
GenePALB2
Chromosome16
Position23,635,460
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 7 Fanconi anemia, complementation group N
(-;TT) 3 2-4 fold higher risk for breast cancer, depending on family history
(TT;TT) 0 common in clinvar