Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10866828
rs10866828
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11778247
rs11778247
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0005612
Disease:
Birth Weight 		G 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs11781222
rs11781222
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11781222
rs11781222
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs11785562
rs11785562
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0424621
Disease:
Body Fat Distribution 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs2942194
rs2942194
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
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: rs2942194
rs2942194
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2942202
rs2942202
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35410017
rs35410017
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8534
rs8534
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs10503728
rs10503728
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs10503728
rs10503728
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0427460
Disease:
Red cell distribution width determination 		C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs2280861
rs2280861
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs11783469
rs11783469
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12549025
rs12549025
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs146287838
rs146287838
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2018490
rs2018490
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2942194
rs2942194
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0427460
Disease:
Red cell distribution width determination 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2942194
rs2942194
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2942194
rs2942194
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs13254494
rs13254494
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs2942202
rs2942202
Entrez Id: 51312
Gene Symbol: SLC25A37
SLC25A37
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012