Variant (rsID / SNP)

rs2524543

rs2524543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDH11Y. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PCDH11YNot classified

Variant type: missense_variant
HGVS: NM_032973.2,c.2749G>T,p.Val917Phe
Allele change: Missense_F885V

Associated conditions / phenotypes

Missense_F885V

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.