Variant (rsID / SNP)

rs7058353

rs7058353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIN4. The table records no clinical significance for this variant.

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Reference-table entries

PIN4Not classified

Variant type: missense_variant
HGVS: NM_001170747.1,c.54C>A,p.Ser18Arg
Allele change: Silent

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.