Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913597
rs121913597
MPZ
0.710 GeneticVariation BEFREE An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val). 11080237

2000
dbSNP: rs121913597
rs121913597
MPZ
A 0.710 CausalMutation CLINVAR