Variant (rsID / SNP)

rs606231348

rs606231348 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS1. Location: chromosome 7, position 142,459,784. Clinical significance in the table: Likely benign.

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Reference-table entries

PRSS1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:142459784
Cytoband: 7q34
HGVS: NM_002769.5(PRSS1):c.360C>T (p.Asn120=)
Allele change: Synonymous_N120N

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.