HDAC9, histone deacetylase 9, 9734

N. diseases: 340; N. variants: 73
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11984041
rs11984041
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0038454
Disease:
Cerebrovascular accident 		0.830 GeneticVariation BEFREE The variant rs556621 but not rs11984041 may increase susceptibility of LAA stroke in the Xinjiang Uyghur population. 25307434 2015
dbSNP: rs11984041
rs11984041
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0038454
Disease:
Cerebrovascular accident 		0.830 GeneticVariation BEFREE A recent Genome-Wide Association study (GWAS) identified rs11984041 on HDAC9 gene to be significantly associated with stroke in a Caucasian population. 23828597 2013
dbSNP: rs11984041
rs11984041
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0038454
Disease:
Cerebrovascular accident 		A 0.830 GeneticVariation GWASDB We identified a new association for large vessel stroke within HDAC9 (encoding histone deacetylase 9) on chromosome 7p21.1 (including further replication in an additional 735 affected individuals and 28,583 controls) (rs11984041; combined P = 1.87 × 10(-11); odds ratio (OR) = 1.42, 95% confidence interval (CI) = 1.28-1.57). 22306652 2012
dbSNP: rs11984041
rs11984041
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0038454
Disease:
Cerebrovascular accident 		0.830 GeneticVariation BEFREE We identified a new association for large vessel stroke within HDAC9 (encoding histone deacetylase 9) on chromosome 7p21.1 (including further replication in an additional 735 affected individuals and 28,583 controls) (rs11984041; combined P = 1.87 × 10(-11); odds ratio (OR) = 1.42, 95% confidence interval (CI) = 1.28-1.57). 22306652 2012
dbSNP: rs11984041
rs11984041
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0038454
Disease:
Cerebrovascular accident 		A 0.830 GeneticVariation GWASCAT We identified a new association for large vessel stroke within HDAC9 (encoding histone deacetylase 9) on chromosome 7p21.1 (including further replication in an additional 735 affected individuals and 28,583 controls) (rs11984041; combined P = 1.87 × 10(-11); odds ratio (OR) = 1.42, 95% confidence interval (CI) = 1.28-1.57). 22306652 2012
dbSNP: rs2073963
rs2073963
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C4083212
Disease:
Alopecia, Male Pattern 		G 0.800 GeneticVariation GWASDB Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
dbSNP: rs2073963
rs2073963
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C4083212
Disease:
Alopecia, Male Pattern 		G 0.800 GeneticVariation GWASCAT Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
dbSNP: rs1178099
rs1178099
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs13233322
rs13233322
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs1528683
rs1528683
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17432268
rs17432268
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0678909
Disease:
Brain Waves 		A 0.700 GeneticVariation GWASCAT Human brain arousal in the resting state: a genome-wide association study. 29703947 2019
dbSNP: rs2240278
rs2240278
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2285440
rs2285440
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2526639
rs2526639
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs302153
rs302153
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs540671238
rs540671238
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0428568
Disease:
Fasting blood glucose measurement 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs67248060
rs67248060
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6951144
rs6951144
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs727851
rs727851
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11764536
rs11764536
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0029410
Disease:
Osteoarthritis of hip 		C 0.700 GeneticVariation GWASCAT Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. 30374069 2018
dbSNP: rs302152
rs302152
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0029410
Disease:
Osteoarthritis of hip 		T 0.700 GeneticVariation GWASCAT Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. 29559693 2018
dbSNP: rs76872642
rs76872642
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0684328
Disease:
Reasoning 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identified loci associated with attention/vigilance (rs830786 within HNF4G), verbal memory (rs67017972 near NDUFS4), and reasoning/problem solving (rs76872642 within HDAC9). 29907492 2018
dbSNP: rs79524815
rs79524815
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0085220
Disease:
Cerebral Amyloid Angiopathy 		G 0.700 GeneticVariation GWASCAT Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. 29458411 2018
dbSNP: rs10278449
rs10278449
Entrez Id: 9734;105375176
Gene Symbol: HDAC9;HDAC9-AS1
HDAC9;HDAC9-AS1
CUI: C0002170
Disease:
Alopecia 		T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs117584427
rs117584427
Entrez Id: 9734
Gene Symbol: HDAC9
HDAC9
CUI: C0002170
Disease:
Alopecia 		G 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017