rs1207534366, LGI4

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)
CUI: C1859721
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)
0.700 CausalMutation CLINVAR
Congenital Camptodactyly
CUI: C0685409
Disease: Congenital Camptodactyly
0.700 CausalMutation CLINVAR
Limited elbow extension and supination
CUI: C4025124
Disease: Limited elbow extension and supination
0.700 CausalMutation CLINVAR
Vertical Talus
CUI: C0240912
Disease: Vertical Talus
0.700 CausalMutation CLINVAR