Variant (rsID / SNP)
rs4512367
rs4512367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PREX2. Location: chromosome 8, position 68,927,592. Clinical significance in the table: association.
Reference-table entries
PREX2Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:68927592
- Cytoband
- 8q13.2
- HGVS
- NM_024870.4(PREX2):c.142-2489C>T
- Allele change
- Silent
Associated conditions / phenotypes
Lip and oral cavity carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.