SLC16A3, solute carrier family 16 member 3, 9123

N. diseases: 122; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4239020
rs4239020
Entrez Id: 9123
Gene Symbol: SLC16A3
SLC16A3
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: rs9674487
rs9674487
Entrez Id: 9123
Gene Symbol: SLC16A3
SLC16A3
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11077983
rs11077983
Entrez Id: 9123
Gene Symbol: SLC16A3
SLC16A3
CUI: C1704436
Disease:
Peripheral Arterial Diseases 		0.700 GeneticVariation GWASCAT Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease. 27082954 2016
dbSNP: rs9747201
rs9747201
Entrez Id: 9123
Gene Symbol: SLC16A3
SLC16A3
CUI: C1704436
Disease:
Peripheral Arterial Diseases 		0.700 GeneticVariation GWASCAT Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease. 27082954 2016