Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555682265
rs1555682265
DCC
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		T 0.700 CausalMutation CLINVAR Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456

2017