Variant (rsID / SNP)

rs662

rs662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PON1. Location: chromosome 7, position 94,937,446. Clinical significance in the table: Benign.

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Reference-table entries

PON1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:94937446
Cytoband: 7q21.3
HGVS: NM_000446.7(PON1):c.575A>G (p.Gln192Arg)
Allele change: Missense_Q192R

Associated conditions / phenotypes

Coronary artery spasm 2, susceptibility to|Coronary artery disease, susceptibility to|Enzyme activity finding

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.