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rs587782018(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs587782018
GeneSTK11
Chromosome19
Position1,220,718
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G) 0 common in clinvar
(G;T) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome