{{Rsnum
|rsid=63750654
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG2
|position=5254956
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,ZNF285B
}}{{omim
|id=142250
|rsnum=63750654
|variant=0027
}}{{ClinVar
|rsid=63750654
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5276186
|CHROM=11
|dbSNPBuildID=137
|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.5276186A>G
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1012; 142250.0027
|CLNSIG=5
|CLNCUI=C1841621
|CLNDBN=Fetal hemoglobin quantitative trait locus 1
|Disease=Fetal hemoglobin quantitative trait locus 1
|CLNACC=RCV000016123.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
}}{{PMID Auto
|PMID=1246351
|Title=Hereditary persistence of foetal haemoglobin with beta-chain synthesis in cis position (Ggamma-beta+-HPFH) in a negro family.
}}