Variant (rsID / SNP)
rs2071403
rs2071403 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPO. Location: chromosome 2, position 1,417,244. Clinical significance in the table: Benign.
Reference-table entries
TPOBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:1417244
- Cytoband
- 2p25.3
- HGVS
- NM_001206744.2(TPO):c.-75A>G
- Allele change
- Silent
Associated conditions / phenotypes
Deficiency of iodide peroxidase
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.