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: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia
0.700 1.000 14 1982 2015
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
MALARIA, SUSCEPTIBILITY TO (finding)
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
Beta Thalassemia, Dominant Inclusion Body Type
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C4693797
Disease: METHEMOGLOBINEMIA, BETA TYPE
METHEMOGLOBINEMIA, BETA TYPE
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C4693822
Disease: ERYTHROCYTOSIS, FAMILIAL, 6
ERYTHROCYTOSIS, FAMILIAL, 6
0.700 0
dbSNP: rs35724775
rs35724775
HBB
0.763 0.080 11 5226924 splice region variant A/G;T snv 1.2E-04
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia
0.700 0