RARB, retinoic acid receptor beta, 5915

N. diseases: 254; N. variants: 34
Disease: Congenital malrotation of intestine ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869025222
rs869025222
Entrez Id: 5915
Gene Symbol: RARB
RARB
CUI: C0221210
Disease:
Congenital malrotation of intestine 		C 0.700 GeneticVariation CLINVAR