Variant (rsID / SNP)
rs1052406
rs1052406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS58. Location: chromosome 7, position 141,952,110. The table records no clinical significance for this variant.
Reference-table entries
PRSS58Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:141952110
- HGVS
- NM_001001317.5,c.657C>T,p.Ala219Ala
- Allele change
- Synonymous_A219A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.