DisGeNET - a database of gene-disease associations

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58, C4693367

Variant: rs886041091 ×

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:

rs886041091

rs886041091

NTRK2

0.800

GeneticVariation

UNIPROT

dbSNP:

rs886041091

rs886041091

NTRK2

G

0.800

GeneticVariation

CLINVAR

dbSNP:

rs886041091

rs886041091

NTRK2

G

0.800

CausalMutation

CLINVAR