FBRSL1, fibrosin like 1, 57666

N. diseases: 21; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11146949
rs11146949
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs4883565
rs4883565
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs61952071
rs61952071
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs74397112
rs74397112
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs79009737
rs79009737
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
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: rs79009737
rs79009737
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs111599055
rs111599055
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0600139
Disease:
Prostate carcinoma 		C 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs117206641
rs117206641
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. 30525989 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0202236
Disease:
Triglycerides measurement 		A 0.700 GeneticVariation GWASCAT Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. 30525989 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs12423664
rs12423664
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASCAT Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. 30289880 2018
dbSNP: rs4883556
rs4883556
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs6560886
rs6560886
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0004238
Disease:
Atrial Fibrillation 		C 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs7295014
rs7295014
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs34390795
rs34390795
Entrez Id: 57666
Gene Symbol: FBRSL1
FBRSL1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016