Gene entry
TG
thyroglobulin
- Chromosome
- 8
- Cytoband
- 8q24.22
- Variants (rsID)
- 72
TG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.22). Its official name is “thyroglobulin”. The reference table lists 72 variants (rsID) for this gene.
Clinically classified variants
20 reference-table entries with clinical significance.
- rs1133076Benignsingle nucleotide variantIodotyrosyl coupling defect
- rs11992497Benignsingle nucleotide variantIodotyrosyl coupling defect
- rs2069556Benignsingle nucleotide variantIodotyrosyl coupling defect
- rs2069569Benignsingle nucleotide variantIodotyrosyl coupling defect
- rs2076740Benignsingle nucleotide variantAutoimmune thyroid disease, susceptibility to, 3|Iodotyrosyl coupling defect
- rs2294024Benignsingle nucleotide variantIodotyrosyl coupling defect
- rs114211101Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect
- rs115436575Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect
- rs138469414Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect
- rs2229843Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect|Premature ovarian failure
- rs3739274Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect
- rs774274702Conflicting interpretationssingle nucleotide variantIodotyrosyl coupling defect
- rs16904774Likely benignsingle nucleotide variantIodotyrosyl coupling defect
- rs121912648Pathogenicsingle nucleotide variantIodotyrosyl coupling defect|Congenital hypothyroidism
- rs121912650Pathogenicsingle nucleotide variantIodotyrosyl coupling defect
- rs137854434Pathogenicsingle nucleotide variantIodotyrosyl coupling defect
- rs2069566Pathogenicsingle nucleotide variantIodotyrosyl coupling defect|Autoimmune thyroid disease, susceptibility to, 3
- rs190914906Uncertain significancesingle nucleotide variantIodotyrosyl coupling defect
- rs192226069Uncertain significancesingle nucleotide variant
- rs200793895Uncertain significancesingle nucleotide variantIodotyrosyl coupling defect
Other listed variants
- rs180204
- rs853308
- rs940074
- rs1810396
- rs1879991
- rs2076737
- rs2294025
- rs2687809
- rs3958179
- rs4074676
- rs6988193
- rs7844210
- rs11782027
- rs16904792
- rs56033214
- rs60703852
- rs72727409
- rs73708398
- rs74591804
- rs75645413
- rs76705738
- rs77027029
- rs77047672
- rs77461631
- rs79405156
- rs79496463
- rs79676842
- rs79970367
- rs80047968
- rs114055648
- rs114322847
- rs114349877
- rs114781869
- rs115015716
- rs116119508
- rs116254142
- rs116340633
- rs117085257
- rs117475219
- rs117512053
- rs117577126
- rs137999469
- rs140180521
- rs141146573
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.