DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Disease: Monoclonal Gammopathy of Undetermined Significance ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs57104699
rs57104699
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026470
Disease:
Monoclonal Gammopathy of Undetermined Significance 		C 0.700 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015
dbSNP: rs4487645
rs4487645
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11
CUI: C0026470
Disease:
Monoclonal Gammopathy of Undetermined Significance 		0.010 GeneticVariation BEFREE Each SNP independently influenced MGUS risk with statistically significant associations (P < .02) for rs1052501, rs2285803, rs4487645, and rs4273077. 24449210 2014