{{Rsnum
|rsid=63750678
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=HBA2
|position=172914
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=63750678
|variant=0069
}}{{ClinVar
|ALT=A
|CHROM=16
|CLNACC=RCV000016983.1
|CLNALLE=1
|CLNDBN=Hemoglobin H disease, nondeletional
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
|CLNHGVS=NC_000016.9:g.222913delT
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0069
|Disease=Hemoglobin H disease
|FwdREF=T
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=AT
|RSPOS=222912
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050360000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=63750678
}}