Variant (rsID / SNP)

rs20567

rs20567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP3D1. Location: chromosome 19, position 2,110,746. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

AP3D1Not classified

Variant type: synonymous_variant
Chromosome / position: 19:2110746
HGVS: NM_001261826.3,c.3135C>T,p.Ser1045Ser
Allele change: Synonymous_S1045S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.