Variant (rsID / SNP)
rs2460827
rs2460827 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SAA4. Location: chromosome 11, position 18,253,176. The table records no clinical significance for this variant.
Reference-table entries
SAA4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:18253176
- HGVS
- NM_006512.4,c.266G>A,p.Cys89Tyr
- Allele change
- Missense_C167Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.