Variant (rsID / SNP)

rs17590

rs17590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPA2. Location: chromosome 7, position 129,916,515. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CPA2Not classified

Variant type: synonymous_variant
Chromosome / position: 7:129916515
HGVS: NM_001869.3,c.633T>C,p.Asp211Asp
Allele change: Synonymous_D211D

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.