rs16926246, HK1

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.
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 10 69333636 intron variant C/T snv 0.12 0.800 1.000 2 2009 2017
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 10 69333636 intron variant C/T snv 0.12 0.800 1.000 1 2009 2009
Corpuscular Hemoglobin Concentration Mean
4389 10 69333636 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
Hemoglobin, CTCAE
CUI: C2239101
Disease: Hemoglobin, CTCAE
26 10 69333636 intron variant C/T snv 0.12 0.700 1.000 1 2009 2009