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rs786202134(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs786202134
GeneSTK11
Chromosome19
Position1,220,490
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(C;C) 0 common in clinvar