STXBP6, syntaxin binding protein 6, 29091

N. diseases: 8; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8017228
rs8017228
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2004925
rs2004925
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200637
Disease:
Monocyte count procedure 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs2004925
rs2004925
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0750880
Disease:
Monocyte count result 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7141943
rs7141943
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200633
Disease:
Neutrophil count (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs8017228
rs8017228
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200638
Disease:
Eosinophil count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200637
Disease:
Monocyte count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200633
Disease:
Neutrophil count (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0023508
Disease:
White Blood Cell Count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200641
Disease:
Blood basophil count (lab test) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0750880
Disease:
Monocyte count result 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2038700
rs2038700
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0857490
Disease:
Granulocyte count 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7141943
rs7141943
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200641
Disease:
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7141943
rs7141943
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10147992
rs10147992
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0750880
Disease:
Monocyte count result 		G 0.700 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs10147992
rs10147992
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200638
Disease:
Eosinophil count procedure 		G 0.700 GeneticVariation GWASDB Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011
dbSNP: rs10147992
rs10147992
Entrez Id: 29091
Gene Symbol: STXBP6
STXBP6
CUI: C0200637
Disease:
Monocyte count procedure 		G 0.700 GeneticVariation GWASCAT Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011