Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3815803

PRSS54

rs3815803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS54. Location: chromosome 16, position 58,318,604. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PRSS54Not classified
Variant type
missense_variant
Chromosome / position
16:58318604
HGVS
NM_001080492.2,c.544A>G,p.Ser182Gly
Allele change
Missense_S83G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.