Variant (rsID / SNP)

rs7493

rs7493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PON2. Location: chromosome 7, position 95,034,775. Clinical significance in the table: Benign.

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Reference-table entries

PON2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:95034775
Cytoband: 7q21.3
HGVS: NM_000305.3(PON2):c.932C>G (p.Ser311Cys)
Allele change: Missense_S299C

Associated conditions / phenotypes

PARAOXONASE 2 POLYMORPHISM

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.