LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10889569
rs10889569
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs1892534
rs1892534
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs6700896
rs6700896
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		A 0.800 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399 2018
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		G 0.800 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399 2018
dbSNP: rs10889569
rs10889569
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046 2013
dbSNP: rs10889569
rs10889569
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASCAT Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046 2013
dbSNP: rs11208659
rs11208659
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0028754
Disease:
Obesity 		C 0.800 GeneticVariation GWASDB Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. 23563609 2013
dbSNP: rs11208659
rs11208659
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0028754
Disease:
Obesity 		C 0.800 GeneticVariation GWASCAT Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. 23563609 2013
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046 2013
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		0.800 GeneticVariation GWASDB Gene-centric analysis identifies variants associated with interleukin-6 levels and shared pathways with other inflammation markers. 23505291 2013
dbSNP: rs1892534
rs1892534
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046 2013
dbSNP: rs6700896
rs6700896
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046 2013
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		A 0.800 GeneticVariation GWASDB Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women. 22939635 2012
dbSNP: rs1805096
rs1805096
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		A 0.800 GeneticVariation GWASCAT Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women. 22939635 2012
dbSNP: rs6700896
rs6700896
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASCAT Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. 19567438 2009
dbSNP: rs6700896
rs6700896
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. 19567438 2009
dbSNP: rs1892534
rs1892534
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		A 0.800 GeneticVariation GWASCAT Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. 18439548 2008
dbSNP: rs1892534
rs1892534
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0201657
Disease:
C-reactive protein measurement 		A 0.800 GeneticVariation GWASDB Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. 18439548 2008
dbSNP: rs11208659
rs11208659
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11208662
rs11208662
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs61779781
rs61779781
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3790438
rs3790438
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs6658330
rs6658330
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018