Variant (rsID / SNP)
rs2302294
rs2302294 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA9. Location: chromosome 17, position 66,985,992. The table records no clinical significance for this variant.
Reference-table entries
ABCA9Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:66985992
- HGVS
- NM_080283.4,c.3917A>C,p.Lys1306Thr
- Allele change
- Missense_K1306T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.