{{Rsnum
|rsid=121908862
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TSHR
|position=81092563
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101928462,TSHR
}}{{omim
|id=603372
|rsnum=121908862
|variant=0005
}}{{ClinVar
|rsid=121908862
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=81558907
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TSHR:7253
|GENE_NAME=TSHR
|GENE_ID=7253
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.81558907T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603372.0005
|CLNSIG=5
|CLNCUI=CN074268
|CLNDBN=Hypothyroidism, congenital, nongoitrous, 1
|Disease=Hypothyroidism
|CLNACC=RCV000006804.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074268:275200:90673
}}