{{Rsnum
|rsid=35826780
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBG2
|position=5253330
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,ZNF285B
}}{{omim
|id=142250
|rsnum=35826780
|variant=0020
}}

{{ClinVar
|rsid=35826780
|Reversed=1
|FwdREF=T
|FwdALT=A,G
|REF=A
|ALT=C,T
|RSPOS=5274560
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=HBG2:3048
|GENE_NAME=HBG2
|GENE_ID=3048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5274560A>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016116.1
|CLNDBN=HEMOGLOBIN F (POOLE)
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=617; 142250.0020
|Disease=HEMOGLOBIN F (POOLE)
}}

{{PMID Auto
|PMID=1127124
|Title=A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | Illumina Human 1M}}