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rs28897759(A;T)

From SNPedia

BRCA2 variant, possibly causal mutation but not definite
Is agenotype
ofrs28897759
GeneBRCA2
Chromosome13
Position32,394,803
mentionedby
Magnitude3.5
ReputeBad
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;T) 3.5 BRCA2 variant, possibly causal mutation but not definite

see discussion at rs28897759