Variant (rsID / SNP)

rs9814557

rs9814557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP2R3A. Location: chromosome 3, position 135,720,540. The table records no clinical significance for this variant.

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Reference-table entries

PPP2R3ANot classified

Variant type: missense_variant
Chromosome / position: 3:135720540
HGVS: NM_002718.5,c.200A>G,p.Asp67Gly
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.