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rs137853082(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs137853082
GeneSTK11
Chromosome19
Position1,220,700
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(C;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G) 0 common in clinvar