Variant (rsID / SNP)
rs6503235
rs6503235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP52. Location: chromosome 17, position 9,515,777. The table records no clinical significance for this variant.
Reference-table entries
CFAP52Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:9515777
- HGVS
- NM_145054.5,c.1006G>A,p.Glu336Lys
- Allele change
- Missense_E336K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.