Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs574861276
rs574861276
PRX
A 0.700 CausalMutation CLINVAR Clinical and genetic spectra of Charcot-Marie-Tooth disease in Chinese Han patients. 27862672

2017
dbSNP: rs574861276
rs574861276
PRX
A 0.700 CausalMutation CLINVAR Periaxin mutations cause a broad spectrum of demyelinating neuropathies. 12112076

2002