Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10168349
rs10168349
PRKCE
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
PRKCE
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
PRKCE
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 1 2009 2017
dbSNP: rs10168349
rs10168349
PRKCE
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: rs4953318
rs4953318
PRKCE
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
PRKCE ; LOC102724965
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
PRKCE
2 46133768 intron variant G/C snv 0.36
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10192064
rs10192064
PRKCE
2 45853263 intron variant T/C snv 0.35
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10495928
rs10495928
PRKCE
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
PRKCE
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: rs10865207
rs10865207
PRKCE
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
PRKCE
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
dbSNP: rs114948639
rs114948639
PRKCE
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
PRKCE
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: rs12623399
rs12623399
PRKCE
2 46122132 intron variant T/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12712955
rs12712955
PRKCE
2 45939182 intron variant A/G snv 0.43
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12712955
rs12712955
PRKCE
2 45939182 intron variant A/G snv 0.43
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12999972
rs12999972
PRKCE
2 45947279 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs13008603
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs13008603
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2017 2017
dbSNP: rs13008603
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2013 2013
dbSNP: rs17034641
rs17034641
PRKCE
2 46145505 intron variant G/A snv 0.16
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2017 2017
dbSNP: rs17034641
rs17034641
PRKCE
2 46145505 intron variant G/A snv 0.16
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2017 2017
dbSNP: rs17737768
rs17737768
PRKCE
2 46129994 intron variant T/C snv 8.1E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2019 2019
dbSNP: rs17799476
rs17799476
PRKCE
2 46125187 intron variant C/G snv 0.13
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016