{{Rsnum
|rsid=121908869
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TSHR
|position=80955802
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSHR
}}{{omim
|id=603372
|rsnum=121908869
|variant=0013
}}{{ClinVar
|rsid=121908869
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=81422146
|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.81422146G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603372.0013
|CLNSIG=5
|CLNCUI=CN074268
|CLNDBN=Hypothyroidism, congenital, nongoitrous, 1
|Disease=Hypothyroidism
|CLNACC=RCV000006812.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074268:275200:90673
}}