DisGeNET - a database of gene-disease associations

Hereditary Motor and Sensory Neuropathy Type I, C0751036

Variant: rs1426969421 ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1426969421

rs1426969421

PMP22

T

0.700

GeneticVariation

CLINVAR

The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy.

2014

dbSNP:

rs1426969421

rs1426969421

PMP22

T

0.700

GeneticVariation

CLINVAR

The PMP22 gene and its related diseases.

2013