Variant (rsID / SNP)

rs17550472

rs17550472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDK16. Clinical significance in the table: Benign.

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Reference-table entries

CDK16Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_006201.5(CDK16):c.-6-279C>T
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.