rs766432, BCL11A

N. diseases: 6
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.
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
220 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.800 1.000 5 2007 2016
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 3 2011 2014
Hemoglobin A2 measurement
CUI: C0474543
Disease: Hemoglobin A2 measurement
5 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 1 2014 2014
Hemoglobin E disease
CUI: C0238159
Disease: Hemoglobin E disease
4 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 1 2010 2010
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 1 2016 2016
Thalassemia
CUI: C0039730
Disease: Thalassemia
18 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.010 1.000 1 2013 2013