{{Rsnum
|rsid=121918586
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RHAG
|position=49619284
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RHAG
}}{{omim
|id=180297
|rsnum=121918586
|variant=0003
}}{{ClinVar
|rsid=121918586
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=49586997
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RHAG:6005
|GENE_NAME=RHAG
|GENE_ID=6005
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.49586997C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000013934.22
|CLNDBN=Rh-null hemolytic anemia, regulator type
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180297.0003
|Disease=Rh-null hemolytic anemia
}}