Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894075
rs104894075
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
G 0.700 CausalMutation CLINVAR Genetic spectrum of hereditary neuropathies with onset in the first year of life. 21840889

2011

dbSNP: rs104894075
rs104894075
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A (disorder)
G 0.700 CausalMutation CLINVAR Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. 11743579

2002