rs9967849, MIR4432HG

N. diseases: 3
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.
Corpuscular Hemoglobin Concentration Mean
4389 2 60382339 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
220 2 60382339 intron variant C/T snv 0.33 0.700 1.000 1 2007 2007
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 2 60382339 intron variant C/T snv 0.33 0.800 1.000 2 2009 2019