Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1182102272
rs1182102272
SLC37A4
TG 0.700 GeneticVariation CLINVAR Mutation analysis in glycogen storage disease type 1 non-a. 11071391

2000
dbSNP: rs1182102272
rs1182102272
SLC37A4
TG 0.700 GeneticVariation CLINVAR Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients. 10923042

2000