Gene: PRKCE ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4953318
rs4953318
PRKCE
5 2 46127912 intron variant A/C snv 0.43 0.800 1.000 2 2009 2017
dbSNP: rs10168349
rs10168349
PRKCE
4 2 46133768 intron variant G/C snv 0.36 0.700 1.000 3 2016 2019
dbSNP: rs10184620
rs10184620
PRKCE
2 2 46131396 intron variant A/G snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs10495928
rs10495928
PRKCE
5 2 46126027 intron variant A/G snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs114948639
rs114948639
PRKCE
3 2 46066687 intron variant C/T snv 7.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs12623399
rs12623399
PRKCE
1 2 46122132 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs12992366
rs12992366
PRKCE
2 2 46138781 intron variant G/A snv 5.3E-02 0.700 1.000 1 2009 2009
dbSNP: rs13008603
rs13008603
PRKCE
5 2 46128709 intron variant C/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs1987070
rs1987070
PRKCE
1 2 46010307 intron variant C/A snv 0.22 0.22 0.700 1.000 1 2019 2019
dbSNP: rs4952800
rs4952800
PRKCE
2 2 46120467 intron variant G/A snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs665783
rs665783
PRKCE
1 2 45654158 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs6753292
rs6753292
PRKCE
1 2 45775021 intron variant T/C snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs71422190
rs71422190
PRKCE
1 2 46088377 intron variant C/G snv 5.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs72808780
rs72808780
PRKCE
1 2 46181868 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019