rs1283391088, HBA1

N. diseases: 4
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.
Erythroid hyperplasia
CUI: C0014800
Disease: Erythroid hyperplasia
3 0.882 0.120 16 176755 synonymous variant C/T snv 1.4E-05 0.010 1.000 1 1993 1993
Microcytic hypochromic anemia (disorder)
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
3 0.882 0.120 16 176755 synonymous variant C/T snv 1.4E-05 0.010 1.000 1 1993 1993
Thalassemia
CUI: C0039730
Disease: Thalassemia
18 0.882 0.120 16 176755 synonymous variant C/T snv 1.4E-05 0.010 1.000 1 1993 1993
Thalassemia Intermedia
CUI: C0271979
Disease: Thalassemia Intermedia
8 0.882 0.120 16 176755 synonymous variant C/T snv 1.4E-05 0.010 1.000 1 2009 2009