{{Rsnum
|rsid=35983258
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG1
|position=5250053
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=35983258
|variant=0027
}}

{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000016177.21
|CLNALLE=1
|CLNDBN=Fetal hemoglobin quantitative trait locus 1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
|CLNHGVS=NC_000011.9:g.5271283G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=1010; 142200.0027
|Disease=Fetal hemoglobin quantitative trait locus 1
|FwdALT=T
|FwdREF=C
|GENEINFO=HBG1:3047
|GENE_ID=3047
|GENE_NAME=HBG1
|REF=G
|RSPOS=5271283
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35983258
}}

{{PMID Auto
|PMID=6210198
|Title=A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia.
|OA=1
}}

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