{{Rsnum
|rsid=41412046
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBA2
|position=173600
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41412046
|variant=0027
}}

{{ClinVar
|rsid=41412046
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=223599
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050168000000000102110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223599A>T
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000500317; 707; 141850.0027
|CLNSIG=255
|CLNCUI=CN077787
|CLNDBN=Hemoglobin H disease, nondeletional
|Disease=Hemoglobin H disease
|CLNACC=RCV000016938.1
|Tags=PM;PMC;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
}}

{{PMID Auto
|PMID=7502632
|Title=Identification of several alpha-globin gene variations in a small Laotian family.
}}

{{PMID Auto
|PMID=8193381
|Title=Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease.
}}

{{PMID Auto
|PMID=11836160
|Title=Clinical phenotypes and molecular characterization of Hb H-Pakse disease.
}}

{{PMID Auto
|PMID=12403487
|Title=Hb Pakse [(alpha2) codon 142 (TAA-->TAT or Term-->Tyr)J in Thai patients with EAbart's disease and Hb H Disease.
}}

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