Variant (rsID / SNP)
rs35598213
rs35598213 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPNE8. Location: chromosome 12, position 39,124,094. The table records no clinical significance for this variant.
Reference-table entries
CPNE8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:39124094
- HGVS
- NM_153634.3,c.789C>T,p.Asn263Asn
- Allele change
- Synonymous_N263N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.