rs7599488, BCL11A

N. diseases: 4
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 0.120 2 60491212 intron variant C/T snv 0.42 0.800 1.000 1 2011 2011
Intelligence
CUI: C0021704
Disease: Intelligence
2093 0.925 0.120 2 60491212 intron variant C/T snv 0.42 0.700 1.000 2 2018 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.925 0.120 2 60491212 intron variant C/T snv 0.42 0.700 1.000 2 2015 2019
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.925 0.120 2 60491212 intron variant C/T snv 0.42 0.700 1.000 1 2011 2011