INO80, INO80 complex ATPase subunit, 54617

N. diseases: 29; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2925345
rs2925345
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0017654
Disease:
Glomerular Filtration Rate 		T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs2928148
rs2928148
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0005612
Disease:
Birth Weight 		A 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs34153025
rs34153025
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35077430
rs35077430
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0017654
Disease:
Glomerular Filtration Rate 		CT 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs6492982
rs6492982
Entrez Id: 54617
Gene Symbol: INO80
INO80
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: rs75322822
rs75322822
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs75322822
rs75322822
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs112925537
rs112925537
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs112925537
rs112925537
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs2928148
rs2928148
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs2928148
rs2928148
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		A 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs476633
rs476633
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0017654
Disease:
Glomerular Filtration Rate 		C 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs476633
rs476633
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		C 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs9796
rs9796
Entrez Id: 54617;112268144
Gene Symbol: INO80;LOC112268144
INO80;LOC112268144
CUI: C1629609
Disease:
Age at menopause 		T 0.700 GeneticVariation GWASCAT Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. 26414677 2015
dbSNP: rs2928148
rs2928148
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C1561643
Disease:
Chronic Kidney Diseases 		0.700 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191 2012
dbSNP: rs199722402
rs199722402
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0014544
Disease:
Epilepsy 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs199722402
rs199722402
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C1843367
Disease:
Poor school performance 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs199722402
rs199722402
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0431350
Disease:
Primary microcephaly 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs730882226
rs730882226
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0014544
Disease:
Epilepsy 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs730882226
rs730882226
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs730882226
rs730882226
Entrez Id: 54617
Gene Symbol: INO80
INO80
CUI: C0431350
Disease:
Primary microcephaly 		G 0.700 GeneticVariation CLINVAR