Variant (rsID / SNP)
rs58830807
rs58830807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS45P. Location: chromosome 3, position 46,783,959. The table records no clinical significance for this variant.
Reference-table entries
PRSS45PNot classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 3:46783959
- HGVS
- NR_160553.1,n.568A>G
- Allele change
- Missense_I190V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.