DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Huntington Disease ×

Variant: rs2269499 ×

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:

rs2269499

rs2269499

HTT

CUI:	C0020179
Disease:	Huntington Disease

Huntington Disease

0.700

GeneticVariation

GWASDB

Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.

2012