rs786205864, STK11

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Peutz-Jeghers Syndrome
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
0.700 CausalMutation CLINVAR Mutations in the human LKB1/STK11 gene. 16110486 2005
Peutz-Jeghers Syndrome
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
0.700 CausalMutation CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174 2004
Peutz-Jeghers Syndrome
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
0.700 CausalMutation CLINVAR Genetic heterogeneity in Peutz-Jeghers syndrome. 10874301 2000