Variant (rsID / SNP)
rs4902359
rs4902359 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAX. Location: chromosome 14, position 65,542,790. Clinical significance in the table: Benign.
Reference-table entries
MAXBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:65542790
- Cytoband
- 14q23.3
- HGVS
- NM_002382.5(MAX):c.*404C>T
- Allele change
- Silent
Associated conditions / phenotypes
Pheochromocytoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.