{{Rsnum
|rsid=2069566
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TG
|position=133017940
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TG
}}{{omim
|id=188450
|rsnum=2069566
|variant=0012
}}{{ClinVar
|rsid=2069566
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=134030185
|CHROM=8
|dbSNPBuildID=96
|SSR=0
|SAO=1
|VP=0x050260000000000102110100
|GENEINFO=TG:7038
|GENE_NAME=TG
|GENE_ID=7038
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.134030185G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188450.0012
|CLNSIG=5
|CLNCUI=C0342194
|CLNDBN=Iodotyrosyl coupling defect
|Disease=Iodotyrosyl coupling defect
|CLNACC=RCV000013537.22
|Tags=PM;S3D;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342194:274700:95716:23536000
}}