{{Rsnum
|rsid=16879498
|Gene=RHAG
|Chromosome=6
|position=49612534
|Orientation=plus
|GMAF=0.05142
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RHAG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 96.9 | 3.1 | 0.0
| HCB | 86.7 | 13.3 | 0.0
| JPT | 91.1 | 8.9 | 0.0
| YRI | 82.3 | 17.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 86.7 | 13.3 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE
|id=180297
|rsnum=16879498
|variant=0009
}}

{{ neighbor
| rsid = 28933991
| distance = 28
}}

{{ClinVar
|rsid=16879498
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=49580247
|CHROM=6
|GMAF=0.0513
|dbSNPBuildID=123
|SSR=0
|SAO=0
|VP=0x050360000000150517110101
|GENEINFO=RHAG:6005
|GENE_NAME=RHAG
|GENE_ID=6005
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.49580247C>T
|CLNSIG=5
|Tags=PM;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9486; 0.05142
|CLNACC=RCV000013940.23
|CLNDBN=Rh-null hemolytic anemia, regulator type
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180297.0009
|COMMON=1
|Disease=Rh-null hemolytic anemia
}}

{{GET Evidence
|gene=RHAG
|aa_change=Val270Ile
|aa_change_short=V270I
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=recessive
|quality_scores=Array
|dbsnp_id=rs16879498
|overall_frequency_n=414
|overall_frequency_d=10758
|overall_frequency=0.038483
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=1
|n_articles_annotated=1
|nblosum100=-4
|autoscore=1
|webscore=N
|summary_short=This variant was found as a compound heterozygote (with G280R) in a Japanese individual with Rhnull disorder.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}