Variant (rsID / SNP)
rs7742033
rs7742033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDSN. Location: chromosome 6, position 31,085,226. The table records no clinical significance for this variant.
Reference-table entries
CDSNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31085226
- HGVS
- NM_001264.5,c.166C>T,p.Leu56Phe
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.