Variant (rsID / SNP)
rs1177562
rs1177562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VPS11. Location: chromosome 11, position 118,949,331. The table records no clinical significance for this variant.
Reference-table entries
VPS11Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:118949331
- HGVS
- NM_001378218.1,c.1989C>T,p.Cys663Cys
- Allele change
- Missense_A650V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
