{{Rsnum
|rsid=34809449
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG1
|position=5254895
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142200
|rsnum=34809449
|variant=0031
}}
{{omim
|id=142250
|rsnum=34809449
|variant=0035
}}
{{omim
|id=142250
|rsnum=34809449
|variant=0046
}}{{ClinVar
|ALT=A,C,T
|CHROM=11
|CLNALLE=1; 3
|CLNHGVS=NC_000011.9:g.5276125G>A; NC_000011.9:g.5276125G>T
|CLNORIGIN=1
|CLNSIG=5
|FwdALT=A,G,T
|FwdREF=C
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=G
|RSPOS=5276125
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM;NOV
|VC=SNV
|VP=0x050168000000000002110104
|WGT=0
|dbSNPBuildID=127
|rsid=34809449
|CLNACC=RCV000016130.24; RCV000016141.24
|CLNDBN=Fetal hemoglobin quantitative trait locus 1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0035; 142250.0046
|Disease=Fetal hemoglobin quantitative trait locus 1
}}{{PMID Auto
|PMID=7516698
|Title=The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma gene.
}}

{{PMID Auto
|PMID=1698280
|Title=A novel C-T transition within the distal CCAAT motif of the G gamma-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression.
|OA=1
}}

{{PMID Auto
|PMID=10335983
|Title=A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.
}}