Variant (rsID / SNP)

rs111033567

rs111033567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS1. Location: chromosome 7, position 142,458,433. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

PRSS1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:142458433
Cytoband: 7q34
HGVS: NM_002769.5(PRSS1):c.68A>G (p.Lys23Arg)
Allele change: Missense_K23R

Associated conditions / phenotypes

Hereditary pancreatitis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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