DNAH11, dynein axonemal heavy chain 11, 8701

N. diseases: 110; N. variants: 109
Disease: Monoclonal Gammopathy of Undetermined Significance ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs57104699
rs57104699 		0.882 0.160 7 21888461 intron variant C/A snv 0.26
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4487645
rs4487645 		0.882 0.200 7 21898622 intron variant C/A;T snv
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014