{{Rsnum
|rsid=34017450
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBG2
|position=5254474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142250
|rsnum=34017450
|variant=0012
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016108.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (LODZ)
|CLNHGVS=NC_000011.9:g.5275704T>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0012
|Disease=HEMOGLOBIN F (LODZ)
|FwdALT=C
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5275704
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34017450
}}

{{PMID Auto
|PMID=1726098
|Title=A second observation of Hb F-Lodz or alpha 2G gamma (2)44(CD3)Ser----Arg.
}}

{{PMID Auto
|PMID=6814491
|Title=Hemoglobin F Lodz (G gamma I 44 Ser replaced by Arg). A newly identified variant from an American infant of Polish descent.
}}

{{on chip | 23andMe v4}}