{{Rsnum
|rsid=35617911
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG2
|position=5254983
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,ZNF285B
}}{{omim
|id=142250
|rsnum=35617911
|variant=0026
}}

{{ClinVar
|rsid=35617911
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=5276213
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=HBG2:3048
|GENE_NAME=HBG2
|GENE_ID=3048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5276213G>C
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1006; 142250.0026
|CLNSIG=5
|CLNCUI=C1841621
|CLNDBN=Fetal hemoglobin quantitative trait locus 1
|Disease=Fetal hemoglobin quantitative trait locus 1
|CLNACC=RCV000016122.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
}}

{{PMID Auto
|PMID=1200028
|Title=A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.
|OA=1
}}

{{PMID Auto
|PMID=6205403
|Title=G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}