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rs730881972(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs730881972
GeneSTK11
Chromosome19
Position1,220,395
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 5.8 Likely miscall in 23andMe v4 (or older) and Ancestry v2c/v2d data; otherwise, STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G) 0 common in clinvar