Variant (rsID / SNP)
rs192861143
rs192861143 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCAF17. Location: chromosome 2, position 172,305,177. Clinical significance in the table: Benign.
Reference-table entries
DCAF17Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:172305177
- Cytoband
- 2q31.1
- HGVS
- NM_025000.4(DCAF17):c.322-14C>T
- Allele change
- Silent
Associated conditions / phenotypes
Woodhouse-Sakati syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.