RAI1, retinoic acid induced 1, 10743

N. diseases: 205; N. variants: 22
Disease: Smith-Magenis syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555566042
rs1555566042
Entrez Id: 10743
Gene Symbol: RAI1
RAI1
CUI: C0795864
Disease:
Smith-Magenis syndrome 		CA 0.700 CausalMutation CLINVAR