Variant (rsID / SNP)

rs77322543

rs77322543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS12. Location: chromosome 4, position 119,237,359. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PRSS12Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:119237359
Cytoband: 4q26
HGVS: NM_003619.4(PRSS12):c.1270G>A (p.Val424Ile)
Allele change: Missense_V424I

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.