{{Rsnum
|rsid=35957832
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG1
|position=5249729
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=35957832
|variant=0022
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016167.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (XINJIANG)
|CLNHGVS=NC_000011.9:g.5270959C>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142200.0022
|Disease=HEMOGLOBIN F (XINJIANG)
|FwdALT=C
|FwdREF=G
|GENEINFO=HBG1:3047
|GENE_ID=3047
|GENE_NAME=HBG1
|REF=C
|RSPOS=5270959
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35957832
}}

{{PMID Auto
|PMID=2448268
|Title=Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variant.
}}

{{on chip | 23andMe v4}}