DisGeNET - a database of gene-disease associations

Huntington Disease, C0020179

Variant: rs1232027 ×

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:

rs1232027

rs1232027

LINC01337

0.700

GeneticVariation

GWASCAT

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

2017