Variant (rsID / SNP)

rs17221346

rs17221346 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCAF17. Location: chromosome 2, position 172,340,419. Clinical significance in the table: Benign.

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Reference-table entries

DCAF17Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:172340419
Cytoband: 2q31.1
HGVS: NM_025000.4(DCAF17):c.*2795T>C
Allele change: Silent

Associated conditions / phenotypes

Woodhouse-Sakati syndrome

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.