Variant (rsID / SNP)

rs215607

rs215607 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE1C. Location: chromosome 7, position 32,338,337. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PDE1CNot classified

Variant type: missense_variant
Chromosome / position: 7:32338337
HGVS: NM_001191058.4,c.11C>T,p.Ala4Val
Allele change: Missense_A4V

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.