Variant (rsID / SNP)
rs3802394
rs3802394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTAP. Location: chromosome 9, position 21,864,535. Clinical significance in the table: Benign.
Reference-table entries
MTAPBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:21864535
- Cytoband
- 9p21.3
- HGVS
- NM_002451.4(MTAP):c.*2522A>G
- Allele change
- Silent
Associated conditions / phenotypes
Diaphyseal medullary stenosis-bone malignancy syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.