Gene: MPZ ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913589
rs121913589
MPZ
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121913602
rs121913602
MPZ
0.010 GeneticVariation BEFREE We found the association of a heterozygous novel MPZ gene point mutation, Ile62Phe in exon 2, with autosomal dominant motor and sensory neuropathy with focally folded myelin sheaths. 10214757

1999