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rs587776659(TG;TG)

From SNPedia
common in clinvar
Is agenotype
ofrs587776659
GeneSTK11
Chromosome19
Position1,221,312
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TG) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(TG;TG) 0 common in clinvar