{{Rsnum
|rsid=586178
|Gene=RHCE
|Chromosome=1
|position=25420739
|Orientation=plus
|GMAF=0.3421
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=RHCE
}}{{omim
|id=111700
|rsnum=586178
|variant=0002
}}

{{GET Evidence
|gene=RHCE
|aa_change=Cys16Trp
|aa_change_short=C16W
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs586178
|overall_frequency_n=2718
|overall_frequency_d=10672
|overall_frequency=0.254685
|n_genomes=26
|n_genomes_annotated=0
|n_haplomes=40
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=0
|webscore=N
}}

{{ClinVar
|ALT=A,C
|CAF=0.6579; 0.3421
|CHROM=1
|CLNACC=RCV000019283.1
|CLNALLE=2
|CLNDBN=RH C/c POLYMORPHISM
|CLNHGVS=NC_000001.11:g.25420739G>C
|CLNSIG=2
|CLNSRC=ClinVar; GTR; OMIM Allelic Variant
|CLNSRCID=NM_020485.4:c.48G\x3d; GTR000500480; 111700.0002
|COMMON=1
|Disease=RH C/c POLYMORPHISM
|FwdALT=A,C
|FwdREF=G
|REF=G
|RSPOS=25420739
|Reversed=0
|SAO=0
|SSR=1
|Tags=PM;S3D;SLO;NSM;REF;SYN;ASP;VLD;G5A;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000b05170516110140
|WGT=1
|dbSNPBuildID=83
|rsid=586178
|CLNORIGIN=1
|GENEINFO=RHCE:6006
|GENE_ID=6006
|GENE_NAME=RHCE
}}

{{on chip | 23andMe v3}}
{{on chip | HumanOmni1Quad}}