CELF1, CUGBP Elav-like family member 1, 10658

N. diseases: 63; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10838725
rs10838725
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.820 GeneticVariation BEFREE A number of genetic variants have previously been identified and associated with the risk of Alzheimer's disease (AD), including rs10838725 in CELF1, rs28834970 in PTK2B, rs17125944 in FERMT2, and rs10410544 in SIRT2 based on genome-wide association studies. 30144538 2018
dbSNP: rs10838725
rs10838725
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0002395
Disease:
Alzheimer's Disease 		0.820 GeneticVariation BEFREE Our first GWAS based cross-disorder analysis for AD and obesity suggests that rs10838725 at the locus CELF1 might be relevant for both disorders. 24788522 2014
dbSNP: rs10838725
rs10838725
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0002395
Disease:
Alzheimer's Disease 		C 0.820 GeneticVariation GWASDB Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. 24162737 2013
dbSNP: rs10838725
rs10838725
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0002395
Disease:
Alzheimer's Disease 		C 0.820 GeneticVariation GWASCAT Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. 24162737 2013
dbSNP: rs11039266
rs11039266
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34958982
rs34958982
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
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: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11039297
rs11039297
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0017654
Disease:
Glomerular Filtration Rate 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs555328608
rs555328608
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs61895110
rs61895110
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0005938
Disease:
Bone Density 		A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1305855
Disease:
Body mass index 		C 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
dbSNP: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C4049938
Disease:
Physical Activity Measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs11537751
rs11537751
Entrez Id: 4722;10658;114971
Gene Symbol: NDUFS3;CELF1;PTPMT1
NDUFS3;CELF1;PTPMT1
CUI: C0020538
Disease:
Hypertensive disease 		T 0.700 GeneticVariation GWASCAT Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. 27618448 2016
dbSNP: rs2868996
rs2868996
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
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: rs7124681
rs7124681
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. 26426971 2015
dbSNP: rs60206633
rs60206633
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0042487
Disease:
Venous Thrombosis 		0.700 GeneticVariation GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
dbSNP: rs77977823
rs77977823
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0042487
Disease:
Venous Thrombosis 		0.700 GeneticVariation GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575 2012
dbSNP: rs10838725
rs10838725
Entrez Id: 10658
Gene Symbol: CELF1
CELF1
CUI: C0028754
Disease:
Obesity 		0.010 GeneticVariation BEFREE Our first GWAS based cross-disorder analysis for AD and obesity suggests that rs10838725 at the locus CELF1 might be relevant for both disorders. 24788522 2014