{{Rsnum
|rsid=2069556
|Gene=TG
|Chromosome=8
|position=132908273
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.4215
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TG
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 19.5 | 49.6 | 31.0
| HCB | 40.1 | 51.8 | 8.0
| JPT | 40.7 | 50.4 | 8.8
| YRI | 94.5 | 5.5 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 40.1 | 51.8 | 8.0
| CHD | 35.8 | 50.5 | 13.8
| GIH | 17.8 | 51.5 | 30.7
| LWK | 90.8 | 9.2 | 0.0
| MEX | 7.3 | 50.9 | 41.8
| MKK | 69.1 | 28.3 | 2.6
| TSI | 16.7 | 45.1 | 38.2
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2069556
|allele=G
|frequency=0.558
|uid=1103652448081
|type=homozygous_SNP
|hugo=TG
|ensembl gene=ENSG00000042832
|ensembl transcript=ENST00000220616
|sift=TOLERATED
|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.
}}

{{GET Evidence
|gene=TG
|aa_change=Asp1312Gly
|aa_change_short=D1312G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2069556
|overall_frequency_n=4903
|overall_frequency_d=10758
|overall_frequency=0.455754
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=4
|autoscore=2
|n_web_uneval=2
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}