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: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.810 GeneticVariation BEFREE Common single-nucleotide polymorphisms (SNPs) at 2p23.3 (rs6746082), 3p22.1 (rs1052501), 3q26.2 (rs10936599), 6p21.33 (rs2285803), 7p15.3 (rs4487645), 17p11.2 (rs4273077), and 22q13.1 (rs877529) have recently been shown to influence MM risk. 24449210 2014
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.810 GeneticVariation GWASDB The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.810 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.810 GeneticVariation GWASCAT The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.810 GeneticVariation GWASDB We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)). 22120009 2011
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.810 GeneticVariation GWASCAT We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)). 22120009 2011
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		T 0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		T 0.800 GeneticVariation GWASCAT Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. 28334899 2017
dbSNP: rs57104699
rs57104699
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.800 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068 2013
dbSNP: rs2285947
rs2285947
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0007137
Disease:
Squamous cell carcinoma 		A 0.800 GeneticVariation GWASDB Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese. 23103227 2012
dbSNP: rs2285947
rs2285947
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0007137
Disease:
Squamous cell carcinoma 		A 0.800 GeneticVariation GWASCAT Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese. 23103227 2012
dbSNP: rs57104699
rs57104699
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASCAT Biological, clinical and population relevance of 95 loci for blood lipids. 20686565 2010
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		G 0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C1445957
Disease:
Serum total cholesterol measurement 		G 0.800 GeneticVariation GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		G 0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs12670798
rs12670798
Entrez Id: 8701;105375183
Gene Symbol: DNAH11;LOC105375183
DNAH11;LOC105375183
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		G 0.800 GeneticVariation GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009