CLVS1, clavesin 1, 157807

N. diseases: 12; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12681792
rs12681792
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C0149931
Disease:
Migraine Disorders 		0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs12681792
rs12681792
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C0149931
Disease:
Migraine Disorders 		0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs12681792
rs12681792
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12681792
rs12681792
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1305855
Disease:
Body mass index 		A 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: rs143346730
rs143346730
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C0337446
Disease:
Tyrosine measurement 		A 0.700 GeneticVariation GWASCAT Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. 31560688 2019
dbSNP: rs74382792
rs74382792
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C4268744
Disease:
Atypical femoral fracture 		G 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture. 31006051 2019
dbSNP: rs13279512
rs13279512
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C0027412
Disease:
Opioid-Related Disorders 		0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. 29478698 2018
dbSNP: rs2931353
rs2931353
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C0202159
Disease:
Parathyroid hormone measurement 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level. 30134803 2018
dbSNP: rs6471932
rs6471932
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
dbSNP: rs142143628
rs142143628
Entrez Id: 157807;100130298
Gene Symbol: CLVS1;LOC100130298
CLVS1;LOC100130298
CUI: C1861172
Disease:
Venous Thromboembolism 		T 0.700 GeneticVariation GWASCAT Among 393 AA VTE cases and 4,941 AA controls, three intragenic SNPs reached genome-wide significance: LEMD3 rs138916004 (OR=3.2; p=1.3E-08), LY86 rs3804476 (OR=1.8; p=2E-08) and LOC100130298 rs142143628 (OR=4.5; p=4.4E-08); all three SNPs validated using internal cross-validation, parametric bootstrap and meta-analysis methods. 28203683 2017
dbSNP: rs4738873
rs4738873
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Genetic studies of body mass index yield new insights for obesity biology. 25673413 2015
dbSNP: rs7830371
rs7830371
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7830371
rs7830371
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7830371
rs7830371
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs7830371
rs7830371
Entrez Id: 157807
Gene Symbol: CLVS1
CLVS1
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014