Variant (rsID / SNP)

rs16889108

rs16889108 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE4D. Location: chromosome 5, position 58,334,922. Clinical significance in the table: Likely benign.

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Reference-table entries

PDE4DLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:58334922
Cytoband: 5q11.2
HGVS: NM_001104631.2(PDE4D):c.809-124C>A
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.