{{Rsnum
|rsid=104894225
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG2
|position=5254380
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,ZNF285B
}}{{omim
|id=142250
|rsnum=104894225
|variant=0039
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016134.1; RCV000030902.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (WAYNESBORO); HEMOGLOBIN F (LESVOS)
|CLNHGVS=NC_000011.9:g.5275610A>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0039; 142250.0045
|Disease=HEMOGLOBIN F (WAYNESBORO); HEMOGLOBIN F (LESVOS)
|FwdALT=C
|FwdREF=T
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=A
|RSPOS=5275610
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=104894225
}}{{PMID Auto
|PMID=7852085
|Title=Hb F-Sassari: a novel G gamma variant with a threonine residue at position gamma 75, characterized by mass spectrometric techniques.
}}

{{PMID Auto
|PMID=8566966
|Title=HbF-Lesvos: an HbF variant due to a novel G gamma mutation (:G gamma 75 ATA-->ACA) detected in a Greek family.
}}