{{Rsnum
|rsid=10495928
|Gene=PRKCE
|Chromosome=2
|position=46126027
|Orientation=plus
|GMAF=0.2952
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PRKCE
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 47.3 | 47.3 | 5.4
| HCB | 74.5 | 22.6 | 2.9
| JPT | 67.0 | 30.4 | 2.7
| YRI | 29.9 | 49.3 | 20.8
| ASW | 16.1 | 58.9 | 25.0
| CHB | 74.5 | 22.6 | 2.9
| CHD | 73.4 | 24.8 | 1.8
| GIH | 47.5 | 46.5 | 6.1
| LWK | 33.9 | 50.5 | 15.6
| MEX | 75.9 | 22.4 | 1.7
| MKK | 36.1 | 46.5 | 17.4
| TSI | 38.2 | 48.0 | 13.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19862010
|Trait=Hemoglobin
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=G
|Pval=7E-13
|OR=0.06
|ORtxt=[0.05-0.08] g/dl increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=20139978
|Trait=Hematological and biochemical traits
|Title=Genome-wide association study of hematological and biochemical traits in a Japanese population
|RiskAllele=G
|Pval=4E-8
|OR=0.21
|ORtxt=[NR] % variance
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10495928
|overall_frequency_n=51
|overall_frequency_d=128
|overall_frequency=0.398438
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=42
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}