{{Rsnum
|rsid=35383398
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=HBB
|position=5226976
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35383398
|variant=0336
}}{{ClinVar
|rsid=35383398
|Reversed=1
|FwdALT=G
|REF=A
|ALT=AC
|RSPOS=5248206
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248206_5248207insC
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016683.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; 790; 141900.0336
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=2901867
|Title=A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA.
}}