Variant (rsID / SNP)
rs536009
rs536009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA5. Location: chromosome 17, position 67,273,882. The table records no clinical significance for this variant.
Reference-table entries
ABCA5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:67273882
- HGVS
- NM_018672.5,c.2494G>T,p.Ala832Ser
- Allele change
- Missense_A832S
Associated conditions / phenotypes
Ovarian Cancer|Ovarian Epithelial Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.