LARP4B, La ribonucleoprotein 4B, 23185

N. diseases: 22; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11253511
rs11253511
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs112889159
rs112889159
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C4268744
Disease:
Atypical femoral fracture 		T 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture. 31006051 2019
dbSNP: rs7908590
rs7908590
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0022661
Disease:
Kidney Failure, Chronic 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. 30604766 2019
dbSNP: rs141536087
rs141536087
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0600139
Disease:
Prostate carcinoma 		GCGCA 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372 2017
dbSNP: rs80282103
rs80282103
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		A 0.700 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372 2017
dbSNP: rs12264390
rs12264390
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0200638
Disease:
Eosinophil 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: rs12264390
rs12264390
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0200641
Disease:
Blood basophil count (lab test) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12762973
rs12762973
Entrez Id: 23185
Gene Symbol: LARP4B
LARP4B
CUI: C0200641
Disease:
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016