RAI1, retinoic acid induced 1, 10743

N. diseases: 205; N. variants: 22
Disease: Coarse facial features ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555565492
rs1555565492
Entrez Id: 10743
Gene Symbol: RAI1
RAI1
CUI: C1845847
Disease:
Coarse facial features 		TG 0.700 CausalMutation CLINVAR