Variant (rsID / SNP)

rs200516654

rs200516654 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCH2. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

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.