{{Rsnum
|rsid=34474104
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG2
|position=5254417
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34474104
|variant=0025
}}

{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000016121.24
|CLNALLE=1
|CLNDBN=Cyanosis, transient neonatal
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151421:613977:280615
|CLNHGVS=NC_000011.9:g.5275647G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=601; 142250.0025
|Disease=Cyanosis
|FwdALT=T
|FwdREF=C
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=G
|RSPOS=5275647
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34474104
}}

{{PMID Auto
|PMID=2483933
|Title=Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant.
}}

{{PMID Auto
|PMID=8811323
|Title=A new case of Hb F-M-Osaka [G gamma 63(E7)His-->Tyr] showed only benign neonatal cyanosis.
}}

{{PMID Auto
|PMID=12603090
|Title=Hb F-M-Osaka [Ggamma63(E7)His --> tyr] in a newborn from southwest France.
}}

{{on chip | 23andMe v2}}