Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		0.800 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		T 0.800 GeneticVariation GWASCAT Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		T 0.800 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		A 0.800 GeneticVariation GWASCAT Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577 2009
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		A 0.800 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577 2009
dbSNP: rs2084312
rs2084312
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34074270
rs34074270
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs9903991
rs9903991
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.700 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: rs2384955
rs2384955
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0201657
Disease:
C-reactive protein measurement 		T 0.700 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: rs35489971
rs35489971
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs35489971
rs35489971
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0337428
Disease:
Fibrinogen assay 		0.700 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs1037171
rs1037171
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0200637
Disease:
Monocyte count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1037171
rs1037171
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0750880
Disease:
Monocyte count result 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2034310
rs2034310
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0200635
Disease:
Lymphocyte Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs749780
rs749780
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs749780
rs749780
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0023508
Disease:
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs749780
rs749780
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0200638
Disease:
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs749780
rs749780
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0200633
Disease:
Neutrophil count (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs77936863
rs77936863
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0857490
Disease:
Granulocyte count 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C1325327
Disease:
fibrinogen activity 		T 0.700 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C1561955
Disease:
Fibrinogen, CTCAE 		T 0.700 GeneticVariation GWASDB Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. 23969696 2013
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C1561955
Disease:
Fibrinogen, CTCAE 		A 0.700 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577 2009
dbSNP: rs10512597
rs10512597
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C1325327
Disease:
fibrinogen activity 		A 0.700 GeneticVariation GWASDB Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. 20031577 2009
dbSNP: rs141171369
rs141171369
Entrez Id: 146722;326624
Gene Symbol: CD300LF;RAB37
CD300LF;RAB37
CUI: C0026769
Disease:
Multiple Sclerosis 		0.010 GeneticVariation BEFREE We identified a missense mutation arginine 33 to glutamine (R33Q) in CD300f by direct sequencing of exon 2 in peripheral blood samples from 50 patients with multiple sclerosis (MS). 29051512 2017