Variant (rsID / SNP)
rs6557351
rs6557351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNKSR3. Location: chromosome 6, position 154,763,401. The table records no clinical significance for this variant.
Reference-table entries
CNKSR3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:154763401
- HGVS
- NM_001368116.1,c.258C>T,p.Asn86Asn
- Allele change
- Synonymous_N80N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.