rs4671393, BCL11A

N. diseases: 11
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 0.790 0.400 2 60493816 intron variant A/C;G snv 0.800 1.000 3 2007 2015
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.790 0.400 2 60493816 intron variant A/C;G snv 0.710 1.000 2 2011 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.790 0.400 2 60493816 intron variant A/C;G snv 0.700 1.000 1 2015 2015
alpha-Thalassemia
CUI: C0002312
Disease: alpha-Thalassemia
37 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2015 2015
alpha^+^ Thalassemia
CUI: C1456873
Disease: alpha^+^ Thalassemia
16 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2015 2015
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2017 2017
Eosinophilic esophagitis
CUI: C0341106
Disease: Eosinophilic esophagitis
40 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2015 2015
Ethylmalonic encephalopathy
CUI: C1865349
Disease: Ethylmalonic encephalopathy
33 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2015 2015
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2017 2017
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2017 2017
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.790 0.400 2 60493816 intron variant A/C;G snv 0.010 1.000 1 2017 2017