RIN3, Ras and Rab interactor 3, 79890

N. diseases: 8; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10498635
rs10498635
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0029401
Disease:
Osteitis Deformans 		0.810 GeneticVariation BEFREE Previous genome-wide association studies identified a locus on chromosome 14q32 tagged by rs10498635 which was significantly associated with susceptibility to PDB in several European populations. 25701875 2015
dbSNP: rs10498635
rs10498635
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0029401
Disease:
Osteitis Deformans 		C 0.810 GeneticVariation GWASDB Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. 21623375 2011
dbSNP: rs10498635
rs10498635
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0029401
Disease:
Osteitis Deformans 		C 0.810 GeneticVariation GWASCAT Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. 21623375 2011
dbSNP: rs10498635
rs10498635
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0029401
Disease:
Osteitis Deformans 		0.810 GeneticVariation GWASDB Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. 20436471 2010
dbSNP: rs11621587
rs11621587
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0042834
Disease:
Vital capacity 		C 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11621587
rs11621587
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11621587
rs11621587
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0016529
Disease:
Forced expiratory volume function 		C 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs11626205
rs11626205
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs117068593
rs117068593
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17184313
rs17184313
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs35629566
rs35629566
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0017654
Disease:
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs61975764
rs61975764
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7143806
rs7143806
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs72699855
rs72699855
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		G 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs754388
rs754388
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C1821417
Disease:
RESTING HEART RATE 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs754388
rs754388
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs72699866
rs72699866
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0005938
Disease:
Bone Density 		G 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: rs11627032
rs11627032
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs754388
rs754388
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0005938
Disease:
Bone Density 		G 0.700 GeneticVariation GWASCAT Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus. 28743860 2017
dbSNP: rs754388
rs754388
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0424678
Disease:
Lean body mass 		G 0.700 GeneticVariation GWASCAT Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus. 28743860 2017
dbSNP: rs754388
rs754388
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		C 0.700 GeneticVariation GWASCAT Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. 28166215 2017
dbSNP: rs11624512
rs11624512
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0023508
Disease:
White Blood Cell 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: rs11624512
rs11624512
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0200638
Disease:
Eosinophil 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: rs11624512
rs11624512
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0857490
Disease:
Granulocyte count 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11624512
rs11624512
Entrez Id: 79890
Gene Symbol: RIN3
RIN3
CUI: C0200641
Disease:
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016