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rs1064796831(CC;CC)

From SNPedia
common in clinvar
Is agenotype
ofrs1064796831
GeneSTK11
Chromosome19
Position1,221,319
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CC) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(CC;CC) 0 common in clinvar