GSE1, Gse1 coiled-coil protein, 23199

N. diseases: 20; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11649660
rs11649660
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16975388
rs16975388
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0205682
Disease:
Waist-Hip Ratio 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs2968426
rs2968426
Entrez Id: 23199;107984830
Gene Symbol: GSE1;LOC107984830
GSE1;LOC107984830
CUI: C0337443
Disease:
Sodium measurement 		G 0.700 GeneticVariation GWASCAT GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits. 31409800 2019
dbSNP: rs3934541
rs3934541
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs61751198
rs61751198
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7198287
rs7198287
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs8054322
rs8054322
Entrez Id: 23199;105371382
Gene Symbol: GSE1;LOC105371382
GSE1;LOC105371382
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs150938367
rs150938367
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0272178
Disease:
Drug-induced neutropenia 		0.700 GeneticVariation GWASCAT Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. 28762467 2018
dbSNP: rs4783183
rs4783183
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0032181
Disease:
Platelet Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7187540
rs7187540
Entrez Id: 23199;197196
Gene Symbol: GSE1;LINC00311
GSE1;LINC00311
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs871290
rs871290
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0202236
Disease:
Triglycerides measurement 		C 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs12447206
rs12447206
Entrez Id: 23199;197196
Gene Symbol: GSE1;LINC00311
GSE1;LINC00311
CUI: C0002170
Disease:
Alopecia 		A 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs1552272
rs1552272
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3060245
rs3060245
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0032181
Disease:
Platelet Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4783186
rs4783186
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0032181
Disease:
Platelet 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: rs4783189
rs4783189
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4843185
rs4843185
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs76563408
rs76563408
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs757859891
rs757859891
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs534448891
rs534448891
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0041296
Disease:
Tuberculosis 		0.010 GeneticVariation BEFREE The (GT)n promoter alleles 2 and 3 (rs534448891), which alter SLC11A1 expression, were significantly associated with tuberculosis (OR=1.47 (1.30-1.66), OR=0.76 (0.65-0.89), respectively) and infectious disease (OR=1.25 (1.10-1.42), OR=0.83 (0.74-0.93), respectively). 25856512 2015
dbSNP: rs709805
rs709805
Entrez Id: 23199
Gene Symbol: GSE1
GSE1
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.010 GeneticVariation BEFREE Statistically significant associations were found between the risk of CRC and the variant alleles of KIAA0182 (rs709805) (odds ratio = 1.57; 95% confidence interval = 1.06-2.78, for the variant homozygotes) and NUP210 genes (rs354476) (odds ratio = 1.36; 95% confidence interval = 1.02-1.82, for the variant homozygotes). 22282400 2012