Variant (rsID / SNP)
rs1062470
rs1062470 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDSN. Location: chromosome 6, position 31,084,435. The table records no clinical significance for this variant.
Reference-table entries
CDSNNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31084435
- HGVS
- NM_001264.5,c.957C>T,p.Tyr319Tyr
- Allele change
- Silent
Associated conditions / phenotypes
Psoriasis 1|Skin Disease|Pustulosis of Palm and Sole|Psoriasis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.