{{Rsnum
|rsid=2076739
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TG
|position=132971804
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TG
}}{{omim
|id=188450
|rsnum=2076739
|variant=0006
}}{{ClinVar
|rsid=2076739
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=133984049
|CHROM=8
|dbSNPBuildID=96
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TG:7038
|GENE_NAME=TG
|GENE_ID=7038
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.133984049T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188450.0006
|CLNSIG=5
|CLNCUI=C0342194
|CLNDBN=Iodotyrosyl coupling defect
|Disease=Iodotyrosyl coupling defect
|CLNACC=RCV000013531.16
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342194:274700:95716:23536000
}}