DisGeNET - a database of gene-disease associations

Childhood Absence Epilepsy, C4281785

Variant: rs8044363 ×

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:

rs8044363

rs8044363

CACNA1H

0.010

GeneticVariation

BEFREE

Moreover, another cSNP rs8044363 was predicted to be connected directly with CAE in a Bayesian network.

2007