{{Rsnum
|rsid=35103459
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG2
|position=5254330
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2,ZNF285B
}}{{omim
|id=142250
|rsnum=35103459
|variant=0034
}}{{ClinVar
|rsid=35103459
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5275560
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG2:3048
|GENE_NAME=HBG2
|GENE_ID=3048
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5275560G>A
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609; 142250.0034
|CLNSIG=5
|CLNCUI=C3151421
|CLNDBN=Cyanosis, transient neonatal
|Disease=Cyanosis
|CLNACC=RCV000016129.21
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151421:613977:280615
}}

{{PMID Auto
|PMID=1385361
|Title=A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr.
}}

{{PMID Auto
|PMID=2470017
|Title=Mutant fetal hemoglobin causing cyanosis in a newborn.
}}

{{PMID Auto
|PMID=2470018
|Title=Hemoglobin FM-Fort Ripley: another lesson from the neonate.
}}

{{on chip | 23andMe v4}}