Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs763868966
rs763868966
GFAP
0.010 GeneticVariation BEFREE We found a novel nonsense mutation (c.1000 G>T, p.(Glu312Ter); also termed p.(E312*)</span>) within a rod domain of GFAP in a 67-year-old Korean man with a history of memory impairment and leukoencephalopathy. 24755947

2015