Variant (rsID / SNP)
rs3748697
rs3748697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPF. Location: chromosome 1, position 214,820,099. The table records no clinical significance for this variant.
Reference-table entries
CENPFNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:214820099
- HGVS
- NM_016343.4,c.7186A>G,p.Asn2396Asp
- Allele change
- Missense_N2396D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.