rs33944208, HBB

N. diseases: 12
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.
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 1.000 15 1984 2017
Hemoglobinopathies
CUI: C0019045
Disease: Hemoglobinopathies
43 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 1.000 11 1984 2017
alpha-Thalassemia
CUI: C0002312
Disease: alpha-Thalassemia
37 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
Beta thalassemia intermedia
CUI: C0472767
Disease: Beta thalassemia intermedia
12 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
Beta Thalassemia, Dominant Inclusion Body Type
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
14 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
beta^+^ Thalassemia
CUI: C3841475
Disease: beta^+^ Thalassemia
44 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
ERYTHROCYTOSIS, FAMILIAL, 6
CUI: C4693822
Disease: ERYTHROCYTOSIS, FAMILIAL, 6
39 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
CUI: C1841621
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
20 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
Heinz Body Anemias
CUI: C0700299
Disease: Heinz Body Anemias
19 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
MALARIA, SUSCEPTIBILITY TO (finding)
CUI: C1970028
Disease: MALARIA, SUSCEPTIBILITY TO (finding)
23 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0
METHEMOGLOBINEMIA, BETA TYPE
CUI: C4693797
Disease: METHEMOGLOBINEMIA, BETA TYPE
13 0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv 0.700 0