{{Rsnum
|rsid=609320
|Gene=RHCE
|Chromosome=1
|position=25390874
|Orientation=plus
|GMAF=0.1621
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=RHCE
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 74.8 | 22.5 | 2.7
| HCB | 57.0 | 39.3 | 3.7
| JPT | 52.7 | 40.2 | 7.1
| YRI | 85.2 | 14.8 | 0.0
| ASW | 74.5 | 25.5 | 0.0
| CHB | 57.0 | 39.3 | 3.7
| CHD | 55.6 | 37.0 | 7.4
| GIH | 90.1 | 9.9 | 0.0
| LWK | 89.9 | 9.2 | 0.9
| MEX | 60.3 | 32.8 | 6.9
| MKK | 93.4 | 6.6 | 0.0
| TSI | 71.3 | 26.7 | 2.0
| HapMapRevision=28
}}{{omim
|id=111700
|rsnum=609320
|variant=0001
}}

{{ClinVar
|rsid=609320
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=25390874
|CHROM=1
|GMAF=0.1621
|dbSNPBuildID=83
|SSR=0
|SAO=1
|VP=0x050368080a05150517110101
|GENEINFO=RHCE:6006
|GENE_NAME=RHCE
|GENE_ID=6006
|WGT=1
|VC=SNV
|CLNALLE=0
|CLNHGVS=NC_000001.11:g.25390874C\x3d
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;PMC;S3D;SLO;NSM;REF;INT;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.8379; 0.1621
|CLNACC=RCV000019282.1
|CLNDBN=RH E/e POLYMORPHISM
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_020485.4:c.676G\x3d; 111700.0001
|COMMON=1
|Disease=RH E/e POLYMORPHISM
}}

{{PMID|21257350|OA=1
}} DNA-based methods in the immunohematology reference laboratory.

{{GET Evidence
|gene=RHCE
|aa_change=Ala226Pro
|aa_change_short=A226P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs609320
|overall_frequency_n=1517
|overall_frequency_d=10758
|overall_frequency=0.141011
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}Rh E/e blood group

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}