ITGA9, integrin subunit alpha 9, 3680

N. diseases: 62; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs197770
rs197770
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs197770
rs197770
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs267567
rs267567
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.800 GeneticVariation GWASDB Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs267567
rs267567
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		A 0.800 GeneticVariation GWASCAT Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. 23139255 2012
dbSNP: rs189897
rs189897
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.710 GeneticVariation GWASDB A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. 20512145 2010
dbSNP: rs189897
rs189897
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.710 GeneticVariation BEFREE Among them, SNP rs189897 showed the strongest association with a P-value of 6.85 x 10(-8) (OR=3.18, 95% CI=1.94-5.21), suggesting that a genetic variation(s) in ITGA9 may influence susceptibility to NPC in the Malaysian Chinese population. 19478819 2009
dbSNP: rs189897
rs189897
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		A 0.710 GeneticVariation GWASDB Among them, SNP rs189897 showed the strongest association with a P-value of 6.85 x 10(-8) (OR=3.18, 95% CI=1.94-5.21), suggesting that a genetic variation(s) in ITGA9 may influence susceptibility to NPC in the Malaysian Chinese population. 19478819 2009
dbSNP: rs2212020
rs2212020
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.710 GeneticVariation BEFREE The combined analysis of the two sets of samples found an SNP in intron 3 of the ITGA9 (integrin-alpha 9) gene, rs2212020, to be strongly associated with NPC (P=8.27 x 10(-7), odds ratio (OR)=2.24, 95% confidence intervals (CI)=1.59-3.15). 19478819 2009
dbSNP: rs2212020
rs2212020
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.710 GeneticVariation GWASDB The combined analysis of the two sets of samples found an SNP in intron 3 of the ITGA9 (integrin-alpha 9) gene, rs2212020, to be strongly associated with NPC (P=8.27 x 10(-7), odds ratio (OR)=2.24, 95% confidence intervals (CI)=1.59-3.15). 19478819 2009
dbSNP: rs155524
rs155524
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0205682
Disease:
Waist-Hip Ratio 		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: rs2507948
rs2507948
Entrez Id: 3680;101928153
Gene Symbol: ITGA9;ITGA9-AS1
ITGA9;ITGA9-AS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs267519
rs267519
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs267539
rs267539
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs539108
rs539108
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs981057
rs981057
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1124374
rs1124374
Entrez Id: 3680;101928153
Gene Symbol: ITGA9;ITGA9-AS1
ITGA9;ITGA9-AS1
CUI: C0596887
Disease:
mathematical ability 		A 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: rs174829
rs174829
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0205682
Disease:
Waist-Hip Ratio 		G 0.700 GeneticVariation GWASCAT Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. 30575882 2018
dbSNP: rs9825420
rs9825420
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9825420
rs9825420
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9825420
rs9825420
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9825420
rs9825420
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs169111
rs169111
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.700 GeneticVariation GWASDB A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. 19478819 2009
dbSNP: rs169188
rs169188
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.700 GeneticVariation GWASDB A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. 19478819 2009
dbSNP: rs189897
rs189897
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C0027439
Disease:
Nasopharyngeal Neoplasms 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. 19478819 2009
dbSNP: rs197757
rs197757
Entrez Id: 3680
Gene Symbol: ITGA9
ITGA9
CUI: C2931822
Disease:
Nasopharyngeal carcinoma 		0.700 GeneticVariation GWASDB A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. 19478819 2009