Variant (rsID / SNP)

rs17197552

rs17197552 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP2R3A. Location: chromosome 3, position 135,722,264. The table records no clinical significance for this variant.

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Reference-table entries

PPP2R3ANot classified

Variant type: missense_variant
Chromosome / position: 3:135722264
HGVS: NM_002718.5,c.1924A>G,p.Ser642Gly
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.