Variant (rsID / SNP)

rs10771381

rs10771381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PZP. Location: chromosome 12, position 9,315,209. The table records no clinical significance for this variant.

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Reference-table entries

PZPNot classified

Variant type: synonymous_variant
Chromosome / position: 12:9315209
HGVS: NM_002864.3,c.2772T>C,p.Ser924Ser
Allele change: Synonymous_S924S

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.