RHOA, ras homolog family member A, 387

N. diseases: 193; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7648841
rs7648841
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007