Variant (rsID / SNP)
rs3743503
rs3743503 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPN. Location: chromosome 16, position 81,056,441. The table records no clinical significance for this variant.
Reference-table entries
CENPNNot classified
- Variant type
- stop_lost
- Chromosome / position
- 16:81056441
- HGVS
- NM_018455.6,c.613T>G,p.Ter205Gluext*?
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.