Variant: rs587781262 

    present in Gene: PRPS1
    present in Chromosome: X
    Position on Chromosome: 107640938
    Alleles of this Variant: A/G

rs587781262 in PRPS1 gene and CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5 PMID 25182139 2015 The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.

rs587781262 in PRPS1 gene and DEAFNESS, X-LINKED 1 (disorder) PMID 25182139 2015 The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.

rs587781262 in PRPS1 gene and Sensorineural Hearing Loss (disorder) PMID 25182139 2015 The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.