rs10495928, PRKCE

N. diseases: 5
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 2 46126027 intron variant A/G snv 0.36 0.800 1.000 2 2009 2016
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2012 2012
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2016 2016
Hemoglobin, CTCAE
CUI: C2239101
Disease: Hemoglobin, CTCAE
26 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2009 2009
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2010 2010