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rs121913315(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121913315
GeneSTK11
Chromosome19
Position1,220,488
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G) 0 common in clinvar
(G;T) 5.8 Cutaneous malignant melanoma designation in Clinvar; cancer risk?