Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs431905504
rs431905504
SLC6A3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		T 0.700 CausalMutation CLINVAR Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524

2012