{{Rsnum
|rsid=61747482
|Gene=TSHR
|Chromosome=14
|position=80955786
|Orientation=plus
|GMAF=0.002296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TSHR
}}{{omim
|id=603372
|rsnum=61747482
|variant=0001
}}{{ClinVar
|rsid=61747482
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=81422130
|CHROM=14
|GMAF=0.0023
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000040116110100
|GENEINFO=TSHR:7253
|GENE_NAME=TSHR
|GENE_ID=7253
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.81422130G>C
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;S3D;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9977; 0.002296
|CLNACC=RCV000006799.1
|CLNDBN=THYROTROPIN RECEPTOR POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603372.0001
|COMMON=1
|Disease=THYROTROPIN RECEPTOR POLYMORPHISM
}}