HBS1L, HBS1 like translational GTPase, 10767

N. diseases: 23; N. variants: 32
Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1547247
rs1547247
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.800 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0032181
Disease:
Platelet Count measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs9376090
rs9376090
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs9376090
rs9376090
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0032181
Disease:
Platelet Count measurement 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.800 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375 2017
dbSNP: rs9376090
rs9376090
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs9376090
rs9376090
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		T 0.800 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375 2017
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		G 0.800 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		G 0.800 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0200695
Disease:
Fetal hemoglobin determination 		C 0.800 GeneticVariation GWASCAT Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels. 26366553 2015
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0032181
Disease:
Platelet Count measurement 		T 0.800 GeneticVariation GWASCAT A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. 24026423 2014
dbSNP: rs7745098
rs7745098
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0019829
Disease:
Hodgkin Disease 		G 0.800 GeneticVariation GWASCAT A combined analysis identifies new HL susceptibility loci mapping to 3p24.1 (rs3806624; P=1.14 × 10(-12), odds ratio (OR)=1.26) and 6q23.3 (rs7745098; P=3.42 × 10(-9), OR=1.21). rs3806624 localizes 5' to the EOMES (eomesodermin) gene within a p53 response element affecting p53 binding. rs7745098 maps intergenic to HBS1L and MYB, a region previously associated with haematopoiesis. 24149102 2013
dbSNP: rs7775698
rs7775698
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASCAT GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
dbSNP: rs7775698
rs7775698
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.800 GeneticVariation GWASCAT GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
dbSNP: rs9376090
rs9376090
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASCAT GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.800 GeneticVariation GWASCAT GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
dbSNP: rs9373124
rs9373124
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.800 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs9399137
rs9399137
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.800 GeneticVariation GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs7775698
rs7775698
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASCAT A genome-wide association study of red blood cell traits using the electronic medical record. 20927387 2010
dbSNP: rs7775698
rs7775698
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010