{{Rsnum
|rsid=104894224
|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,ZNF285B
|Status=Merged
|Merged=34474104
}}{{omim
|id=142250
|rsnum=104894224
|variant=0025
}}{{ClinVar
|rsid=104894224
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5275647
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=050260080801000002110100
|GENEINFO=HBG2:3048; LOC100653006:100653006
|GENE_NAME=HBG2; LOC100653006
|GENE_ID=3048; 100653006
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5275647G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142250.0025
|CLNSIG=5
|CLNCUI=C3151421
|CLNDBN=Cyanosis, transient neonatal
|Disease=Cyanosis
|CLNACC=SCV000036389.1
|Tags=RV;PM;S3D;NSM;INT;OTHERKG;LSD;OM
}}