{{Rsnum
|rsid = 1061234
|Gene=HBG1
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=5249456
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|desc=HBG1 POLYMORPHISM
|id=142200
|rsnum=1061234
|variant=0001
}}
{{omim
|desc=HEMOGLOBIN F (SARDINIA)
|id=142200
|rsnum=1061234
|variant=0018
}}
{{omim
| id = 142200
| variant = 0032
| desc    = HEMOGLOBIN F (CHARLOTTE)
| rsnum   = 1061234
}}
{{omim
| id = 142250
| variant = 0045
| desc    = HEMOGLOBIN F (LESVOS)
| rsnum   = 1061234
}}
{{ neighbor
| rsid = 28933078
| distance = 49
}}

{{omim
|id=142200
|rsnum=1061234
|variant=0037
}}

{{omim
|id=142250
|rsnum=1061234
|variant=0039
}}

{{ClinVar
|rsid=1061234
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5270686
|CHROM=11
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050360000000070102110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5270686G>A
|CLNORIGIN=1
|CLNSRCID=
142200.0001; 142200.0018; 142200.0032; 142200.0037
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016145.1; RCV000016180.1; RCV000016185.1; RCV000030904.1
|Tags=RV;PM;S3D;SLO;VLD;G5A;G5;GNO;OTHERKG;LSD;OM
|CLNDBN=HBG1 POLYMORPHISM; HEMOGLOBIN F (CHARLOTTE); HEMOGLOBIN F (PORTO TORRES); HEMOGLOBIN F (SARDINIA)
|CLNSRC=OMIM Allelic Variant
|Disease=HBG1 POLYMORPHISM; HEMOGLOBIN F (CHARLOTTE); HEMOGLOBIN F (PORTO TORRES); HEMOGLOBIN F (SARDINIA)
}}

{{GET Evidence
|gene=HBG1
|aa_change=Thr76Ile
|aa_change_short=T76I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1061234
|overall_frequency_n=2794
|overall_frequency_d=7770
|overall_frequency=0.359588
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=87
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}