Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202041339
rs202041339
NAGS
C 0.700 GeneticVariation CLINVAR Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. 12594532

2003