DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10485986
rs10485986
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs10499535
rs10499535
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
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: rs1060503041
rs1060503041
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1060503063
rs1060503063
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1060503064
rs1060503064
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1128226
rs1128226
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs1128226
rs1128226
Entrez Id: 8701;55536
Gene Symbol: DNAH11;CDCA7L
DNAH11;CDCA7L
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.700 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs1164659091
rs1164659091
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1175443221
rs1175443221
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure. 22184204 2012
dbSNP: rs1175443221
rs1175443221
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR New DNAH11 mutations in primary ciliary dyskinesia with normal axonemal ultrastructure. 20513915 2010
dbSNP: rs1175443221
rs1175443221
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations. 18022865 2008
dbSNP: rs11761264
rs11761264
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11763022
rs11763022
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11763025
rs11763025
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11763665
rs11763665
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11763709
rs11763709
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11766053
rs11766053
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11769521
rs11769521
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs11770434
rs11770434
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.700 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0149781
Disease:
Spontaneous pneumothorax 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C2678473
Disease:
CILIARY DYSKINESIA, PRIMARY, 7 (disorder) 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0035455
Disease:
Rhinitis 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0581354
Disease:
Recurrent sinusitis 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0018681
Disease:
Headache 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1178187217
rs1178187217
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0149514
Disease:
Acute bronchitis 		A 0.700 GeneticVariation CLINVAR