Variant (rsID / SNP)
rs4572747
rs4572747 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VPS8. Location: chromosome 3, position 184,700,356. The table records no clinical significance for this variant.
Reference-table entries
VPS8Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 3:184700356
- HGVS
- NM_001009921.3,c.3423A>C,p.Ala1141Ala
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_A1139A|Synonymous_A1141A|Synonymous_A568A|Synonymous_A1128A|Synonymous_A1141A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.