RHOA, ras homolog family member A, 387

N. diseases: 193; N. variants: 16
Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6784820
rs6784820
Entrez Id: 387;6988
Gene Symbol: RHOA;TCTA
RHOA;TCTA
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008