DisGeNET - a database of gene-disease associations

MENTAL RETARDATION, AUTOSOMAL DOMINANT 48, C4540321

Gene: RAC1 ×

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:

rs1554263326

RAC1

0.800

GeneticVariation

UNIPROT

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

28886345

2017

dbSNP:

rs1554263624

RAC1

0.800

GeneticVariation

UNIPROT

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

28886345

2017

dbSNP:

rs1554263625

RAC1

0.800

GeneticVariation

UNIPROT

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

28886345

2017

dbSNP:

rs1554263626

RAC1

0.800

GeneticVariation

UNIPROT

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

28886345

2017

dbSNP:

rs1554264268

RAC1

0.800

GeneticVariation

UNIPROT

RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes.

28886345

2017

dbSNP:

rs1554263326

RAC1

0.800

CausalMutation

CLINVAR

dbSNP:

rs1554263624

RAC1

0.800

CausalMutation

CLINVAR

dbSNP:

rs1554263625

RAC1

0.800

CausalMutation

CLINVAR

dbSNP:

rs1554263625

RAC1

0.800

CausalMutation

CLINVAR

dbSNP:

rs1554263626

RAC1

0.800

CausalMutation

CLINVAR

dbSNP:

rs1554264268

RAC1

0.800

CausalMutation

CLINVAR