RAB5C, RAB5C, member RAS oncogene family, 5878

N. diseases: 24; N. variants: 18
Disease: Vitiligo ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11079035
rs11079035
Entrez Id: 5878
Gene Symbol: RAB5C
RAB5C
CUI: C0042900
Disease:
Vitiligo 		A 0.700 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757 2016