Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		0.700 1.000 15 1984 2017
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies 		0.700 1.000 11 1984 2017
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C4693797
Disease: METHEMOGLOBINEMIA, BETA TYPE
METHEMOGLOBINEMIA, BETA TYPE 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C1970028
Disease: MALARIA, SUSCEPTIBILITY TO (finding)
MALARIA, SUSCEPTIBILITY TO (finding) 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C4693822
Disease: ERYTHROCYTOSIS, FAMILIAL, 6
ERYTHROCYTOSIS, FAMILIAL, 6 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0472767
Disease: Beta thalassemia intermedia
Beta thalassemia intermedia 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C1841621
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias 		0.700 0
dbSNP: rs33944208
rs33944208
HBB
0.752 0.080 11 5227159 5 prime UTR variant G/A;C;T snv
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.700 0