DisGeNET - a database of gene-disease associations

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22, C4015062

Variant: rs587777788 ×

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:

rs587777788

rs587777788

ATP5F1A

0.800

GeneticVariation

UNIPROT

Targeted exome sequencing of suspected mitochondrial disorders.

2013

dbSNP:

rs587777788

rs587777788

ATP5F1A

C

0.800

CausalMutation

CLINVAR