R3HDM2, R3H domain containing 2, 22864

N. diseases: 24; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs12313306
rs12313306
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs12313306
rs12313306
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs12315434
rs12315434
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12371805
rs12371805
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12371805
rs12371805
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2122982
rs2122982
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs4760355
rs4760355
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		G 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs540730
rs540730
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs540730
rs540730
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0202236
Disease:
Triglycerides measurement 		C 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs540730
rs540730
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0001948
Disease:
Alcohol consumption 		C 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs7974833
rs7974833
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs7974833
rs7974833
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs11613352
rs11613352
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018