{{Rsnum
|rsid=35301433
|Gene=TG
|Chromosome=8
|position=132871398
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TG
}}{{Venter SNP
|rsid=35301433
|allele=G
|frequency=
|uid=1103652448013
|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 v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}