Variant (rsID / SNP)
rs2304256
rs2304256 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYK2. Location: chromosome 19, position 10,475,652. Clinical significance in the table: Benign.
Reference-table entries
TYK2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:10475652
- Cytoband
- 19p13.2
- HGVS
- NM_003331.5(TYK2):c.1084G>T (p.Val362Phe)
- Allele change
- Missense_V362F
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.