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rs55716624(C;T)

From SNPedia

BRCA2 variant of unknown clinical significance
Is agenotype
ofrs55716624
GeneBRCA2
Chromosome13
Position32,356,496
mentionedby
Magnitude2.2
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2.2 BRCA2 variant of unknown clinical significance