Variant (rsID / SNP)
rs495337
rs495337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA2. Location: chromosome 20, position 48,522,330. The table records no clinical significance for this variant.
Reference-table entries
SPATA2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:48522330
- HGVS
- NM_001135773.2,c.1389C>T,p.Cys463Cys
- Allele change
- Synonymous_C463C
Associated conditions / phenotypes
Pustulosis of Palm and Sole|Psoriasis|Psoriasis 12|Psoriatic Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.