{{Rsnum
|rsid=2069561
|Gene=TG
|Chromosome=8
|position=132963038
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.3678
|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 | 20.4 | 47.8 | 31.9
| HCB | 10.2 | 49.6 | 40.1
| JPT | 8.0 | 51.3 | 40.7
| YRI | 0.0 | 2.0 | 98.0
| ASW | 1.8 | 26.3 | 71.9
| CHB | 10.2 | 49.6 | 40.1
| CHD | 12.0 | 45.4 | 42.6
| GIH | 19.8 | 46.5 | 33.7
| LWK | 0.0 | 0.0 | 0.0
| MEX | 31.0 | 56.9 | 12.1
| MKK | 0.0 | 17.9 | 82.1
| TSI | 25.5 | 46.1 | 28.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=2069561
|allele=A
|frequency=0.458
|uid=1103652448242
|type=homozygous_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.
}}

{{GET Evidence
|gene=TG
|aa_change=Asp1838Asn
|aa_change_short=D1838N
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2069561
|overall_frequency_n=4027
|overall_frequency_d=10758
|overall_frequency=0.374326
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=26
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.061
|genetests_testable=Y
|nblosum100=-1
|autoscore=1
|webscore=N
}}

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