DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555652216
rs1555652216
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C4479640
Disease:
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		0.700 GeneticVariation UNIPROT Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456 2017