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rs587781856(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs587781856
GeneSTK11
Chromosome19
Position1,220,482
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;A) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(A;A) 0 common in clinvar