SLC7A2, solute carrier family 7 member 2, 6542

N. diseases: 30; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56335308
rs56335308
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0201874
Disease:
Amino acids measurement 		G 0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019
dbSNP: rs56335308
rs56335308
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0523801
Disease:
Ornithine measurement 		G 0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019
dbSNP: rs7838611
rs7838611
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0201874
Disease:
Amino acids measurement 		0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019
dbSNP: rs75902664
rs75902664
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs2720499
rs2720499
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASCAT Genome-wide association study of leukotriene modifier response in asthma. 26031901 2016