PRKCE, protein kinase C epsilon, 5581

N. diseases: 112; N. variants: 51
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10168349
rs10168349
2 46133768 intron variant G/C snv 0.36
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.800 1.000 3 2009 2018
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.800 1.000 2 2009 2016
dbSNP: rs4953318
rs4953318
2 46127912 intron variant A/C snv 0.43
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 2 2009 2017
dbSNP: rs10168349
rs10168349
2 46133768 intron variant G/C snv 0.36
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 3 2016 2019
dbSNP: rs13008603
rs13008603
2 46128709 intron variant C/A snv 0.10
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 2 2012 2013
dbSNP: rs4953318
rs4953318
2 46127912 intron variant A/C snv 0.43
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 2 2012 2017
dbSNP: rs687914
rs687914
2 45651621 5 prime UTR variant G/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2019 2019
dbSNP: rs10168349
rs10168349
2 46133768 intron variant G/C snv 0.36
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2018 2018
dbSNP: rs10168349
rs10168349
2 46133768 intron variant G/C snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10183887
rs10183887
2 46134669 intron variant T/A snv 0.28
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10184620
rs10184620
2 46131396 intron variant A/G snv 0.12
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10184620
rs10184620
2 46131396 intron variant A/G snv 0.12
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10192064
rs10192064
2 45853263 intron variant T/C snv 0.35
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement
0.700 1.000 1 2019 2019
dbSNP: rs10198247
rs10198247
2 46135538 intron variant A/G snv 0.28
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10495927
rs10495927
2 46125360 intron variant A/G snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE
0.700 1.000 1 2009 2009
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2010 2010
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs10495928
rs10495928
2 46126027 intron variant A/G snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10495929
rs10495929
2 46145035 intron variant G/A snv 0.15
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10495930
rs10495930
2 46145536 intron variant A/G snv 0.16
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10865207
rs10865207
2 45829110 intron variant G/A snv 0.78
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs114948639
rs114948639
2 46066687 intron variant C/T snv 7.2E-03
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs114948639
rs114948639
2 46066687 intron variant C/T snv 7.2E-03
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs114948639
rs114948639
2 46066687 intron variant C/T snv 7.2E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016