Variant (rsID / SNP)
rs6549590
rs6549590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTN3. Location: chromosome 3, position 74,413,676. The table records no clinical significance for this variant.
Reference-table entries
CNTN3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:74413676
- HGVS
- NM_001393376.1,c.1155A>G,p.Gln385Gln
- Allele change
- Synonymous_Q385Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.