HBS1L, HBS1 like translational GTPase, 10767

N. diseases: 49; N. variants: 124
Disease: Finding of Mean Corpuscular Hemoglobin ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASDB 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: 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: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASDB 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: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.800 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525 2012
dbSNP: rs7775698
rs7775698
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010
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: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		C 0.800 GeneticVariation GWASCAT Sequence variants in three loci influence monocyte counts and erythrocyte volume. 19853236 2009
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		G 0.800 GeneticVariation GWASCAT Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs7776054
rs7776054
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		G 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs148394396
rs148394396
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12664956
rs12664956
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs1331309
rs1331309
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		G 0.700 GeneticVariation GWASCAT Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. 28548082 2017
dbSNP: rs9389268
rs9389268
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. 28453575 2017
dbSNP: rs567333455
rs567333455
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		CA 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6904897
rs6904897
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs13220662
rs13220662
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525 2012
dbSNP: rs1547247
rs1547247
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525 2012