SMOX, spermine oxidase, 54498

N. diseases: 91; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1741344
rs1741344
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6084653
rs6084653
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6084653
rs6084653
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6084653
rs6084653
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8118315
rs8118315
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10211774
rs10211774
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs1051904
rs1051904
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs13038292
rs13038292
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs13043612
rs13043612
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs1741314
rs1741314
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs1765003
rs1765003
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs6084646
rs6084646
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6515865
rs6515865
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0206161
Disease:
Reticulocyte 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: rs1741309
rs1741309
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0497327
Disease:
Dementia 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. 25188341 2014
dbSNP: rs1741344
rs1741344
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010
dbSNP: rs1741344
rs1741344
Entrez Id: 54498
Gene Symbol: SMOX
SMOX
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Hundreds of variants clustered in genomic loci and biological pathways affect human height. 20881960 2010