rs10172646, BCL11A

N. diseases: 2
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 60493622 intron variant G/A snv 0.64 0.800 1.000 3 2007 2011
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 1.000 0.080 2 60493622 intron variant G/A snv 0.64 0.700 1.000 1 2011 2011