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: 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: 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: 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