DisGeNET - a database of gene-disease associations

NTRK2, neurotrophic receptor tyrosine kinase 2, 4915

N. diseases: 284; N. variants: 42

Disease: Epilepsy ×

Variant: rs10868235 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs10868235

Entrez Id:	4915
Gene Symbol:	NTRK2

NTRK2

CUI:	C0014544
Disease:

Epilepsy

0.010

GeneticVariation

BEFREE

Patients with epilepsy showed a trend for a difference in rs10868235 allelic distribution compared to controls without epilepsy.

28863320

2017