rs1242982981, CLEC12A

N. diseases: 4
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.
IgM monoclonal gammopathy of uncertain significance
CUI: C0563312
Disease: IgM monoclonal gammopathy of uncertain significance
3 0.851 0.160 12 9984989 missense variant C/T snv 0.010 1.000 1 2013 2013
Monoclonal Gammopathy of Undetermined Significance
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
20 0.851 0.160 12 9984989 missense variant C/T snv 0.010 1.000 1 2013 2013
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.851 0.160 12 9984989 missense variant C/T snv 0.010 1.000 1 2013 2013
Waldenstrom Macroglobulinemia
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
15 0.851 0.160 12 9984989 missense variant C/T snv 0.010 1.000 1 2013 2013