ELOVL4, ELOVL fatty acid elongase 4, 6785

N. diseases: 111; N. variants: 15
Disease: Erythrokeratodermia with ataxia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692036
rs1131692036
Entrez Id: 6785
Gene Symbol: ELOVL4
ELOVL4
CUI: C1851481
Disease:
Erythrokeratodermia with ataxia 		C 0.700 CausalMutation CLINVAR