Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205864
rs786205864
STK11
GC 0.700 CausalMutation CLINVAR Mutations in the human LKB1/STK11 gene. 16110486

2005
dbSNP: rs786205864
rs786205864
STK11
GC 0.700 CausalMutation CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174

2004
dbSNP: rs786205864
rs786205864
STK11
GC 0.700 CausalMutation CLINVAR Genetic heterogeneity in Peutz-Jeghers syndrome. 10874301

2000