DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Prion Diseases ×

Variant: rs1799990 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1799990

rs1799990

PRNP

CUI:	C0162534
Disease:	Prion Diseases

Prion Diseases

0.860

GeneticVariation

GWASDB

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

2012