Variant (rsID / SNP)
rs2236007
rs2236007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX9. Location: chromosome 14, position 37,132,769. Clinical significance in the table: Benign.
Reference-table entries
PAX9Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:37132769
- Cytoband
- 14q13.3
- HGVS
- NM_001372076.1(PAX9):c.631+41G>A
- Allele change
- Silent
Associated conditions / phenotypes
Partial congenital absence of teeth
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.