rs7606173, BCL11A

N. diseases: 5
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 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.800 1.000 1 2011 2011
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 3 2016 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 3 2016 2019
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 1 2011 2011
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 0.700 1.000 1 2009 2009