Gene: G6PC2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144254880
rs144254880
SPC25 ; G6PC2
0.010 GeneticVariation BEFREE The Arg79Gln variant alters an amino acid mutation of which, in G6PC1, has previously been shown to cause glycogen storage disease type 1a. 27611587

2016