rs587779413, TCIRG1

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.
Congenital neutropenia
CUI: C0340970
Disease: Congenital neutropenia
11 0.925 0.080 11 68050224 missense variant C/A snv 0.700 1.000 1 2014 2014
Neutropenia, Severe Congenital, Autosomal Dominant 1
CUI: C1859966
Disease: Neutropenia, Severe Congenital, Autosomal Dominant 1
26 0.925 0.080 11 68050224 missense variant C/A snv 0.700 1.000 1 2014 2014