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rs587776657(GGTC;GGTC)

From SNPedia
common in clinvar
Is agenotype
ofrs587776657
GeneSTK11
Chromosome19
Position1,220,701
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TCGG) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(GGTC;GGTC) 0 common in clinvar
(TCGG;TCGG) 0 common/normal