{{Rsnum
|rsid=35848600
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBD
|position=5232980
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBD
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=142000
|rsnum=35848600
|variant=0006
}}

{{ClinVar
|rsid=35848600
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=5254210
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=HBD:3045
|GENE_NAME=HBD
|GENE_ID=3045
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5254210G>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016192.1
|CLNDBN=HEMOGLOBIN A(2) FITZROY
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=681; 142000.0006
|Disease=HEMOGLOBIN A(2) FITZROY
}}

{{PMID Auto
|PMID=6548205
|Title=Hemoglobin A2 Fitzroy delta 142 Ala----Asp: a new delta-chain variant.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}