Variant (rsID / SNP)

rs3213831

rs3213831 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PZP. Location: chromosome 12, position 9,316,773. The table records no clinical significance for this variant.

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Reference-table entries

PZPNot classified

Variant type: missense_variant
Chromosome / position: 12:9316773
HGVS: NM_002864.3,c.2570A>G,p.Asn857Ser
Allele change: Missense_N857S

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.