Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863225029
rs863225029
PMP22
C 0.700 CausalMutation CLINVAR Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis. 23965407

2013
dbSNP: rs863225029
rs863225029
PMP22
C 0.700 CausalMutation CLINVAR Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. 21252112

2011
dbSNP: rs863225029
rs863225029
PMP22
C 0.700 CausalMutation CLINVAR Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis. 21149811

2010