rs34813378, C1QB

N. diseases: 1
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.
C1q DEFICIENCY
CUI: C3150902
Disease: C1q DEFICIENCY
8 1.000 1 22661354 missense variant G/A snv 1.2E-05 1.4E-05 0.700 0