Variant (rsID / SNP)
rs312185
rs312185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP2S1. Location: chromosome 19, position 47,342,867. The table records no clinical significance for this variant.
Reference-table entries
AP2S1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:47342867
- HGVS
- NM_001301078.3,c.164T>G,p.Ile55Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.