Variant (rsID / SNP)
rs2549887
rs2549887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPN. Location: chromosome 16, position 81,061,827. The table records no clinical significance for this variant.
Reference-table entries
CENPNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 16:81061827
- HGVS
- NM_001100625.3,c.862G>A,p.Glu288Lys
- Allele change
- Missense_E268K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.