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rs1060499961(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs1060499961
GeneSTK11
Chromosome19
Position1,207,042
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;C) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(C;C) 0 common in clinvar