DisGeNET - a database of gene-disease associations

rs189139, SH3BP2

N. diseases: 2

Disease: Huntington Disease ×

Source: CURATED ×

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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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Huntington Disease

CUI:	C0020179
Disease:	Huntington Disease

0.700

GeneticVariation

GWASDB

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

2012