rs57104699, 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 0.160 7 21888461 intron variant C/A snv 0.26 0.800 1.000 2 2011 2015
Monoclonal Gammopathy of Undetermined Significance
20 0.882 0.160 7 21888461 intron variant C/A snv 0.26 0.700 1.000 1 2015 2015
Paraproteinemias
CUI: C0030489
Disease: Paraproteinemias
9 0.882 0.160 7 21888461 intron variant C/A snv 0.26 0.700 1.000 1 2015 2015