DisGeNET - a database of gene-disease associations

Gilles de la Tourette syndrome, C0040517

Variant: rs779610480 ×

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:

rs779610480

rs779610480

SLITRK1

0.010

GeneticVariation

BEFREE

Only one patient with familial TS was heterozygous for a novel 708C > T (Ile236Ile) nucleotide variant.

2006