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Variant (rsID / SNP)

rs55698418

PRKD3

rs55698418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKD3. Location: chromosome 2, position 37,543,593. The table records no clinical significance for this variant.

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Reference-table entries

PRKD3Not classified
Variant type
synonymous_variant
Chromosome / position
2:37543593
HGVS
NM_005813.6,c.75T>C,p.Ala25Ala
Allele change
Synonymous_A25A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.