SLC7A1, solute carrier family 7 member 1, 6541

N. diseases: 46; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3803266
rs3803266
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7338758
rs7338758
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9508495
rs9508495
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs63418562
rs63418562
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs63418562
rs63418562
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
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
dbSNP: rs41318021
rs41318021
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0085580
Disease:
Essential Hypertension 		0.010 GeneticVariation BEFREE The rs41318021 polymorphism in the SLC7A1 gene was not associated with essential hypertension in 50-year-old subjects. 23841815 2013
dbSNP: rs41318021
rs41318021
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The association of rs41318021 with hypertension was therefore studied in a Finnish cohort. 23841815 2013
dbSNP: rs765151049
rs765151049
Entrez Id: 6541
Gene Symbol: SLC7A1
SLC7A1
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE To search for miRNAs that may be involved in the pathogenesis of Parkinsons disease (PD), we utilized miRNA microarrays to identify potential gene expression changes in 115 annotated miRNAs in PD-associated Caenorhabditis elegans models that either overexpress human A53T alpha-synuclein or have mutations within the vesicular catecholamine transporter (cat-1) or parkin (pdr-1) ortholog. 20091141 2010