rs1336698, FGF14

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.
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
85 1.000 0.040 13 102211398 intron variant C/T snv 0.85 0.700 1.000 1 2011 2011