{{Rsnum
|rsid=137853163
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=THRA
|position=40089333
|Gene_s=THRA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=137853163
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=38245586
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|GENEINFO=THRA:7067
|GENE_NAME=THRA
|GENE_ID=7067
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.38245586G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=190120.0002
|CLNSIG=5
|CLNCUI=CN120649
|CLNDBN=Hypothyroidism, congenital, nongoitrous, 6
|Disease=Hypothyroidism
|CLNACC=RCV000022801.22
|Tags=PM;S3D;OTHERKG;LSD
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280817:614450:97927
}}