DisGeNET - a database of gene-disease associations

NTRK1, neurotrophic receptor tyrosine kinase 1, 4914

N. diseases: 443; N. variants: 59

Disease: Multiple Sclerosis ×

Variant: rs926103 ×

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:

rs926103

rs926103

Entrez Id:	4914;9047
Gene Symbol:	NTRK1;SH2D2A

NTRK1;SH2D2A

CUI:	C0026769
Disease:

Multiple Sclerosis

0.010

GeneticVariation

BEFREE

The GA(16)-rs926103()A haplotype was associated with MS in Norwegians (OR 1.4, P=0.04).

2008