{{Rsnum
|rsid=34160180
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GTT)
|geno3=(GTT;GTT)
|Gene=HBB
|position=5226950
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34160180
|variant=0076
}}{{ClinVar
|rsid=34160180
|Reversed=1
|FwdREF=TTG
|FwdALT=
|REF=CAAC
|ALT=C
|RSPOS=5248179
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248180_5248182delAAC
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016337.1; RCV000016338.1
|CLNDBN=HEMOGLOBIN FREIBURG; HEMOGLOBIN M (FREIBURG)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0076
|Disease=HEMOGLOBIN FREIBURG; HEMOGLOBIN M (FREIBURG)
}}{{PMID Auto
|PMID=5919752
|Title=Hemoglobin Freiburg: abnormal hemoglobin due to deletion of a single amino acid residue.
}}