DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Huntington Disease ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	118
Gene Symbol:	ADD1

ADD1

CUI:	C0020179
Disease:	Huntington Disease

Huntington Disease

0.130

GeneticVariation

GWASDB

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

2012