rs41469945, HBA2

N. diseases: 3
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.
Anemia
CUI: C0002871
Disease: Anemia
94 0.925 0.080 16 173581 missense variant T/C;G snv 0.700 0
Heinz Body Anemias
CUI: C0700299
Disease: Heinz Body Anemias
19 0.925 0.080 16 173581 missense variant T/C;G snv 0.700 0
Splenomegaly
CUI: C0038002
Disease: Splenomegaly
19 0.925 0.080 16 173581 missense variant T/C;G snv 0.700 0