{{Rsnum
|rsid=34975911
|Gene=HBD
|Chromosome=11
|position=5234560
|Orientation=minus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HBD
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 1.8 | 98.2
| 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 | 0.0 | 0.0
| 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=34975911
|variant=0030
}}

{{ClinVar
|rsid=34975911
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5255790
|CHROM=11
|GMAF=0.0014
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000040517110100
|GENEINFO=HBD:3045
|GENE_NAME=HBD
|GENE_ID=3045
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5255790A>G
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=991; 142000.0030
|CLNSIG=5
|CLNCUI=C0271990
|CLNDBN=delta Thalassemia
|Disease=delta Thalassemia
|CLNACC=RCV000016224.24
|Tags=RV;PM;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271990:16427007
|COMMON=1
}}

{{PMID Auto
|PMID=1515647
|Title=Delta-thalassemia caused by disruption of the site for an erythroid-specific transcription factor, GATA-1, in the delta-globin gene promoter.
}}

{{PMID Auto
|PMID=3476164
|Title=A delta-globin gene derived from patients with homozygous delta zero-thalassemia functions normally on transient expression in heterologous cells.
}}

{{PMID Auto
|PMID=6158498
|Title=Homozygous delta thalassemia in Japan.
}}

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