Variant (rsID / SNP)
rs17686569
rs17686569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA5. Location: chromosome 17, position 67,290,840. The table records no clinical significance for this variant.
Reference-table entries
ABCA5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:67290840
- HGVS
- NM_018672.5,c.1451A>G,p.Gln484Arg
- Allele change
- Missense_Q484R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.