{{Rsnum
|rsid=35378915
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5249974
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=35378915
|variant=0026
}}

{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000016171.24; RCV000016172.24; RCV000016173.24
|CLNALLE=1
|CLNDBN=Fetal hemoglobin quantitative trait locus 1; Sardinian hpfh; Greek hpfh
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
|CLNHGVS=NC_000011.9:g.5271204C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142200.0026
|Disease=Fetal hemoglobin quantitative trait locus 1; Sardinian hpfh; Greek hpfh
|FwdALT=A
|FwdREF=G
|GENEINFO=HBG1:3047
|GENE_ID=3047
|GENE_NAME=HBG1
|REF=C
|RSPOS=5271204
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35378915
}}

{{PMID Auto
|PMID=1201197
|Title=Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
}}

{{PMID Auto
|PMID=2452784
|Title=A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia.
}}

{{PMID Auto
|PMID=2469505
|Title=The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin.
}}

{{PMID Auto
|PMID=2578619
|Title=G to A substitution in the distal CCAAT box of the A gamma-globin gene in Greek hereditary persistence of fetal haemoglobin.
}}

{{PMID Auto
|PMID=2578620
|Title=A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.
}}

{{PMID Auto
|PMID=3181130
|Title=The -117 mutation in Greek HPFH affects the binding of three nuclear factors to the CCAAT region of the gamma-globin gene.
|OA=1
}}

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