{{Rsnum
|rsid=121918668
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TSHB
|position=115033507
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSHB
}}{{omim
|id=188540
|rsnum=121918668
|variant=0001
}}{{ClinVar
|rsid=121918668
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=115033507
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260020a05000002110100
|GENEINFO=TSHB:7252
|GENE_NAME=TSHB
|GENE_ID=7252
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.115033507G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000549.4:c.145G>A; NM_001277991.1:c.-439G>A; 188540.0001
|CLNSIG=5
|CLNCUI=C0271789
|CLNDBN=Secondary hypothyroidism
|Disease=Secondary hypothyroidism
|CLNACC=RCV000013521.23
|Tags=PM;S3D;NSM;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271789:275100:ORPHA90674:82598004
}}