RFX6, regulatory factor X6, 222546

N. diseases: 39; N. variants: 13
Disease: Congenital anomaly of gastrointestinal tract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562146029
rs1562146029
Entrez Id: 222546
Gene Symbol: RFX6
RFX6
CUI: C0012241
Disease:
Congenital anomaly of gastrointestinal tract 		G 0.700 CausalMutation CLINVAR