{{Rsnum
|rsid=33974602
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5249561
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=33974602
|variant=0033
}}
{{omim
|id=142250
|rsnum=33974602
|variant=0030
}}{{ClinVar
|rsid=33974602
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5270791
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5270791C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016181.1
|CLNDBN=HEMOGLOBIN F (WOODSTOCK)
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=628; 142200.0033
|Disease=HEMOGLOBIN F (WOODSTOCK)
}}

{{PMID Auto
|PMID=1802881
|Title=Gamma chain abnormalities and gamma-globin gene rearrangements in newborn babies of various populations.
}}

{{on chip | 23andMe v4}}