{{Rsnum
|rsid = 11535853
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Status = Merged
|Merged = 2076740
|Gene = TG
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=8
|position=132971813
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TG
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 36.3 | 50.4 | 13.3
| HCB | 65.7 | 29.9 | 4.4
| JPT | 64.6 | 31.9 | 3.5
| YRI | 19.7 | 44.2 | 36.1
| ASW | 38.6 | 38.6 | 22.8
| CHB | 65.7 | 29.9 | 4.4
| CHD | 61.5 | 33.9 | 4.6
| GIH | 56.4 | 39.6 | 4.0
| LWK | 29.1 | 52.7 | 18.2
| MEX | 51.7 | 39.7 | 8.6
| MKK | 21.8 | 46.8 | 31.4
| TSI | 41.2 | 46.1 | 12.7
| HapMapRevision=28
}}

{{Venter SNP
|rsid=11535853
|allele=T
|frequency=0.417
|uid=1103652448295
|type=heterozygous_SNP
|hugo=TG
|ensembl gene=ENSG00000042832
|ensembl transcript=ENST00000220616
|sift=
|disease=Defects in TG are a cause of some forms of goiter (MIM:188450). Goiter is an enlargement of the thyroid gland. This is sometimes linked to hypothyroidism.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}