Variant (rsID / SNP)

rs702722

rs702722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLK2. Location: chromosome 5, position 57,754,851. The table records no clinical significance for this variant.

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Reference-table entries

PLK2Not classified

Variant type: synonymous_variant
Chromosome / position: 5:57754851
HGVS: NM_006622.4,c.339T>C,p.Ile113Ile
Allele change: Synonymous_I113I

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.