Variant (rsID / SNP)
rs13173706
rs13173706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGA2. Location: chromosome 5, position 52,386,458. Clinical significance in the table: Benign.
Reference-table entries
ITGA2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:52386458
- Cytoband
- 5q11.2
- HGVS
- NM_002203.4(ITGA2):c.*29G>A
- Allele change
- Silent
Associated conditions / phenotypes
Platelet-type bleeding disorder 9
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.