SEMA5A, semaphorin 5A, 9037

N. diseases: 85; N. variants: 24
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs112941079
rs112941079
Entrez Id: 9037;100505806
Gene Symbol: SEMA5A;SNHG18
SEMA5A;SNHG18
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs17329170
rs17329170
Entrez Id: 9037;100113384;100505806
Gene Symbol: SEMA5A;SNORD123;SNHG18
SEMA5A;SNORD123;SNHG18
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs10062083
rs10062083
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12189232
rs12189232
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12519207
rs12519207
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs13359124
rs13359124
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs16882096
rs16882096
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17238371
rs17238371
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6555593
rs6555593
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6863413
rs6863413
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs6876019
rs6876019
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs886511
rs886511
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs899575
rs899575
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs899576
rs899576
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs899576
rs899576
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs922548
rs922548
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs983856
rs983856
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs984425
rs984425
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12653117
rs12653117
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0026896
Disease:
Myasthenia Gravis 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations. 26562150 2016
dbSNP: rs2463505
rs2463505
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C1519383
Disease:
Smoking Behaviors 		0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs2463505
rs2463505
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0037369
Disease:
Smoking 		0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs16882243
rs16882243
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0264408
Disease:
Childhood asthma 		0.700 GeneticVariation GWASDB Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. 23829686 2013
dbSNP: rs1806119
rs1806119
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs433755
rs433755
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0201874
Disease:
Amino acids measurement 		C 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs433755
rs433755
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0162701
Disease:
Polysomnography 		C 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012