RHOA, ras homolog family member A, 387

N. diseases: 193; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1987628
rs1987628
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals. 29520040 2019
dbSNP: rs11716948
rs11716948
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs7623659
rs7623659
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs7623687
rs7623687
Entrez Id: 387;6988
Gene Symbol: RHOA;TCTA
RHOA;TCTA
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs7623687
rs7623687
Entrez Id: 387;6988
Gene Symbol: RHOA;TCTA
RHOA;TCTA
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. 28714974 2017
dbSNP: rs7623687
rs7623687
Entrez Id: 387;6988
Gene Symbol: RHOA;TCTA
RHOA;TCTA
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975 2017
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1458155
Disease:
Mammary Neoplasms 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1458155
Disease:
Mammary Neoplasms 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519951
rs1057519951
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519952
rs1057519952
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0009404
Disease:
Colorectal Neoplasms 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519952
rs1057519952
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1458155
Disease:
Mammary Neoplasms 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519952
rs1057519952
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519952
rs1057519952
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519952
rs1057519952
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0152018
Disease:
Esophageal carcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0152018
Disease:
Esophageal carcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C0152018
Disease:
Esophageal carcinoma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C1458155
Disease:
Mammary Neoplasms 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519953
rs1057519953
Entrez Id: 387
Gene Symbol: RHOA
RHOA
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016