rs10168349, PRKCE

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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 2 46133768 intron variant G/C snv 0.36 0.800 1.000 3 2009 2018
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 2 46133768 intron variant G/C snv 0.36 0.700 1.000 3 2016 2019
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 2 46133768 intron variant G/C snv 0.36 0.700 1.000 1 2012 2012
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 2 46133768 intron variant G/C snv 0.36 0.700 1.000 1 2018 2018