{{Rsnum
|rsid=35687396
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBG1
|position=5254652
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=35687396
|variant=0037
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000016132.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN F (COSENZA)
|CLNHGVS=NC_000011.9:g.5275882C>T
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0037
|Disease=HEMOGLOBIN F (COSENZA)
|FwdALT=A
|FwdREF=G
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=C
|RSPOS=5275882
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35687396
}}

{{PMID Auto
|PMID=1726095
|Title=Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant.
}}

{{on chip | 23andMe v4}}