Variant (rsID / SNP)
rs12720355
rs12720355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYK2. Location: chromosome 19, position 10,472,452. Clinical significance in the table: Benign.
Reference-table entries
TYK2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:10472452
- Cytoband
- 19p13.2
- HGVS
- NM_003331.5(TYK2):c.1953C>T (p.Ile651=)
- Allele change
- Synonymous_I651I
Associated conditions / phenotypes
Immunodeficiency 35
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.