rs11886868, BCL11A

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.
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
220 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.800 1.000 3 2007 2011
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.710 1.000 2 2011 2016
Cardiac Arrest
CUI: C0018790
Disease: Cardiac Arrest
50 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.020 1.000 2 2016 2016
alpha-Thalassemia
CUI: C0002312
Disease: alpha-Thalassemia
37 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2015 2015
alpha^+^ Thalassemia
CUI: C1456873
Disease: alpha^+^ Thalassemia
16 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2015 2015
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2017 2017
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2016 2016
Beta thalassemia intermedia
CUI: C0472767
Disease: Beta thalassemia intermedia
12 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2010 2010
beta^+^ Thalassemia
CUI: C3841475
Disease: beta^+^ Thalassemia
44 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2016 2016
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2016 2016
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2017 2017
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.752 0.280 2 60493111 intron variant C/T snv 0.65 0.010 1.000 1 2017 2017