DisGeNET - a database of gene-disease associations

ALTERNATING HEMIPLEGIA OF CHILDHOOD 1, C3549447

Variant: rs28934002 ×

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:

rs28934002

rs28934002

ATP1A2

0.800

GeneticVariation

UNIPROT

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

2004

dbSNP:

rs28934002

rs28934002

ATP1A2

A

0.800

CausalMutation

CLINVAR