SLC14A2, solute carrier family 14 member 2, 8170

N. diseases: 71; N. variants: 37
Disease: Systolic Pressure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7236548
rs7236548
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8093563
rs8093563
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2193635
rs2193635
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017