Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554646653
rs1554646653
GLDC
C 0.700 GeneticVariation CLINVAR The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. 27362913

2017
dbSNP: rs1554646653
rs1554646653
GLDC
C 0.700 GeneticVariation CLINVAR Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia. 26179960

2015