Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773398906
rs773398906
DGKE ; C17orf67
0.010 GeneticVariation BEFREE The other siblings harbored a homozygous I22M mutation, and one of them had evidence of lower motor neuron disease. 12391347

2002