rs4487645, DNAH11

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.882 0.200 7 21898622 intron variant C/A;T snv 0.810 1.000 4 2011 2014
Primary amyloidosis
CUI: C0268381
Disease: Primary amyloidosis
11 0.882 0.200 7 21898622 intron variant C/A;T snv 0.700 1.000 1 2017 2017
Monoclonal Gammopathy of Undetermined Significance
20 0.882 0.200 7 21898622 intron variant C/A;T snv 0.010 1.000 1 2014 2014