rs33949869, HBB

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.
Hemoglobinopathies
CUI: C0019045
Disease: Hemoglobinopathies
43 1.000 11 5225606 missense variant A/C;G;T snv 0.700 1.000 4 1975 1997
ERYTHROCYTOSIS, FAMILIAL, 6
CUI: C4693822
Disease: ERYTHROCYTOSIS, FAMILIAL, 6
39 1.000 11 5225606 missense variant A/C;G;T snv 0.700 0