{{Rsnum
|rsid=121918669
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TSHB
|position=115033456
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSHB
}}{{omim
|id=188540
|rsnum=121918669
|variant=0002
}}{{ClinVar
|rsid=121918669
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=115033456
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260020605000002110100
|GENEINFO=TSHB:7252
|GENE_NAME=TSHB
|GENE_ID=7252
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.115033456G>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000549.4:c.94G>T; NM_001277991.1:c.-490G>T; 188540.0002
|CLNSIG=5
|CLNCUI=C0271789
|CLNDBN=Secondary hypothyroidism
|Disease=Secondary hypothyroidism
|CLNACC=RCV000013522.21
|Tags=PM;S3D;NSN;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271789:275100:ORPHA90674:82598004
}}