Disease: Multiple congenital anomalies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs775499191
rs775499191
Entrez Id: 23057
Gene Symbol: NMNAT2
NMNAT2
CUI: C0000772
Disease:
Multiple congenital anomalies 		TG 0.700 GeneticVariation CLINVAR Identification of a novel human nicotinamide mononucleotide adenylyltransferase. 12359228 2002