Variant (rsID / SNP)

rs7786497

rs7786497 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRSS58. Location: chromosome 7, position 141,957,504. The table records no clinical significance for this variant.

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Reference-table entries

PRSS58Not classified

Variant type: synonymous_variant
Chromosome / position: 7:141957504
HGVS: NM_001001317.5,c.24T>C,p.Ala8Ala
Allele change: Synonymous_A8A

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.