Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554263326
rs1554263326
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
A 0.800 CausalMutation CLINVAR
dbSNP: rs1554263624
rs1554263624
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
G 0.800 CausalMutation CLINVAR
dbSNP: rs1554263625
rs1554263625
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
C 0.800 CausalMutation CLINVAR
dbSNP: rs1554263625
rs1554263625
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
A 0.800 CausalMutation CLINVAR
dbSNP: rs1554263626
rs1554263626
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
G 0.800 CausalMutation CLINVAR
dbSNP: rs1554264268
rs1554264268
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
A 0.800 CausalMutation CLINVAR
dbSNP: rs1554263326
rs1554263326
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
0.800 GeneticVariation UNIPROT RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. 28886345 2017
dbSNP: rs1554263624
rs1554263624
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
0.800 GeneticVariation UNIPROT RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. 28886345 2017
dbSNP: rs1554263625
rs1554263625
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
0.800 GeneticVariation UNIPROT RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. 28886345 2017
dbSNP: rs1554263626
rs1554263626
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
0.800 GeneticVariation UNIPROT RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. 28886345 2017
dbSNP: rs1554264268
rs1554264268
Entrez Id: 5879
Gene Symbol: RAC1
RAC1
CUI: C4540321
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 48
0.800 GeneticVariation UNIPROT RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes. 28886345 2017