NFIX, nuclear factor I X, 4784

N. diseases: 183; N. variants: 33
Disease: Marshall-Smith syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122869
rs398122869
Entrez Id: 4784
Gene Symbol: NFIX
NFIX
CUI: C0265211
Disease:
Marshall-Smith syndrome 		C 0.700 CausalMutation CLINVAR