Variant (rsID / SNP)
rs17054397
rs17054397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITK. Location: chromosome 5, position 156,680,876. Clinical significance in the table: Benign.
Reference-table entries
ITKBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:156680876
- Cytoband
- 5q33.3
- HGVS
- NM_005546.4(ITK):c.*1188A>G
- Allele change
- Silent
Associated conditions / phenotypes
Lymphoproliferative syndrome 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.