rs13019832, BCL11A

N. diseases: 3
Source: INFERRED ×
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.
Intelligence
CUI: C0021704
Disease: Intelligence
2 60483436 intron variant G/A snv 0.39 0.700 1.000 2 2018 2019
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
2 60483436 intron variant G/A snv 0.39 0.700 1.000 1 2007 2007
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
2 60483436 intron variant G/A snv 0.39 0.700 1.000 1 2009 2009