rs2210913, FCRL3

N. diseases: 2
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.
Immunoglobulin A deficiency (disorder)
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
25 0.925 0.080 1 157699203 intron variant C/T snv 0.56 0.700 1.000 1 2016 2016
Selective immunoglobulin A deficiency
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
23 0.925 0.080 1 157699203 intron variant C/T snv 0.56 0.700 1.000 1 2016 2016