rs1427407, 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 0.827 0.120 2 60490908 intron variant T/C;G snv 0.800 1.000 3 2007 2014
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.827 0.120 2 60490908 intron variant T/C;G snv 0.710 1.000 3 2011 2019
alpha-Thalassemia
CUI: C0002312
Disease: alpha-Thalassemia
37 0.827 0.120 2 60490908 intron variant T/C;G snv 0.010 1.000 1 2017 2017
alpha^+^ Thalassemia
CUI: C1456873
Disease: alpha^+^ Thalassemia
16 0.827 0.120 2 60490908 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Cardiac Arrest
CUI: C0018790
Disease: Cardiac Arrest
50 0.827 0.120 2 60490908 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Sickle Cell Trait
CUI: C0037054
Disease: Sickle Cell Trait
16 0.827 0.120 2 60490908 intron variant T/C;G snv 0.010 1.000 1 2015 2015