HTT, huntingtin, 3064

N. diseases: 188; N. variants: 32
Disease: Huntington Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2798296
rs2798296
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease 		0.700 GeneticVariation GWASDB Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. 22387017 2012