DisGeNET - a database of gene-disease associations

Prion Diseases, C0162534

Variant: rs2075650 ×

Source: ALL

Results per page

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:

rs2075650

rs2075650

TOMM40

0.700

GeneticVariation

GWASDB

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

2012