Variant (rsID / SNP)
rs874898
rs874898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX8. Location: chromosome 2, position 113,974,196. Clinical significance in the table: Benign.
Reference-table entries
PAX8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:113974196
- Cytoband
- 2q14.1
- HGVS
- NM_003466.4(PAX8):c.*1914C>G
- Allele change
- Silent
Associated conditions / phenotypes
Hypothyroidism, congenital, nongoitrous, 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.