Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057520039
rs1057520039
STK11
T 0.700 CausalMutation CLINVAR Disease pattern in Danish patients with Peutz-Jeghers syndrome. 26979979

2016
dbSNP: rs1057520039
rs1057520039
STK11
T 0.700 CausalMutation CLINVAR Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. 9887330

1999