Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554309093
rs1554309093
FIG4
T 0.700 CausalMutation CLINVAR Genetic heterogeneity of motor neuropathies. 28251916

2017
dbSNP: rs1554309093
rs1554309093
FIG4
T 0.700 CausalMutation CLINVAR The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. 25614874

2014