Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386833587
rs386833587
A 0.700 CausalMutation CLINVAR The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. 27362913

2017

dbSNP: rs386833587
rs386833587
A 0.700 GeneticVariation CLINVAR Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia. 26179960

2015

dbSNP: rs386833587
rs386833587
A 0.700 CausalMutation CLINVAR Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia. 26179960

2015

dbSNP: rs386833587
rs386833587
A 0.700 CausalMutation CLINVAR Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia. 16450403

2006

dbSNP: rs386833587
rs386833587
A 0.700 GeneticVariation CLINVAR Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia. 16450403

2006

dbSNP: rs386833587
rs386833587
A 0.700 CausalMutation CLINVAR Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathy. 16601880

2006

dbSNP: rs386833587
rs386833587
A 0.700 GeneticVariation CLINVAR Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathy. 16601880

2006