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rs137853075(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs137853075
GeneSTK11
Chromosome19
Position1,221,237
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 5.8 Likely miscall in Ancestry v2c data; otherwise, STK11 gene mutation associated with Peutz-Jeghers syndrome
(C;C) 0 common in clinvar