rs137853077, STK11

N. diseases: 1
Source: BEFREE ×
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
0.810 GeneticVariation BEFREE Effects of Peutz-Jeghers syndrome (PJS) causing missense mutations L67P, L182P, G242V and R297S on the structural dynamics of LKB1 (Liver kinase B1) protein. 29447078 2019