Variant: rs104894714 

    present in Gene: PRX
    present in Chromosome: 19
    Position on Chromosome: 40395495
    Alleles of this Variant: G/A

rs104894714 in PRX gene and CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F PMID 11133365 2001 Periaxin mutations cause recessive Dejerine-Sottas neuropathy.

rs104894714 in PRX gene and Charcot-Marie-Tooth disease type 4 PMID 15197604 2004 Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease.

PMID 11133365 2001 Periaxin mutations cause recessive Dejerine-Sottas neuropathy.