SLC28A1, solute carrier family 28 member 1, 9154

N. diseases: 33; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs117436140
rs117436140
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1451538
rs1451538
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs1451538
rs1451538
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs1451538
rs1451538
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0428886
Disease:
Mean blood pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs3825876
rs3825876
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0027947
Disease:
Neutropenia 		0.010 GeneticVariation BEFREE For SLC28A1 rs3825876 (G>A), AA patients have a higher risk of neutropenia than GA and GG patients (P=0.02, hazard ratio: 1.51, 95% confidence interval: 1.06-2.16). 30889042 2019
dbSNP: rs3825876
rs3825876
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0023530
Disease:
Leukopenia 		0.010 GeneticVariation BEFREE For SLC28A1 rs3825876 (G>A), AA patients have a higher risk of neutropenia than GA and GG patients (P=0.02, hazard ratio: 1.51, 95% confidence interval: 1.06-2.16). 30889042 2019
dbSNP: rs4980345
rs4980345
Entrez Id: 9154
Gene Symbol: SLC28A1
SLC28A1
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE One interaction, between rs7164883 at the HCN4 locus and rs4980345 at the SLC28A1 locus, was found to be significantly associated with AF in the discovery cohorts (interaction OR = 1.44, 95% CI: 1.27-1.65, P = 4.3 × 10<sup>-8</sup>). 27824142 2016