{{Rsnum
|rsid=35321913
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBG1
|position=5250052
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=35321913
|variant=0030
}}

{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000016178.24
|CLNALLE=1
|CLNDBN=Fetal hemoglobin quantitative trait locus 1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1841621:141749
|CLNHGVS=NC_000011.9:g.5271282G>C
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=1011; 142200.0030
|Disease=Fetal hemoglobin quantitative trait locus 1
|FwdALT=G
|FwdREF=C
|GENEINFO=HBG1:3047
|GENE_ID=3047
|GENE_NAME=HBG1
|REF=G
|RSPOS=5271282
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35321913
}}

{{PMID Auto
|PMID=2224140
|Title=The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C----G substitution at nucleotide -195 of the A gamma-globin gene.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}