Variant (rsID / SNP)

rs41274622

rs41274622 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDH15. Location: chromosome 10, position 55,570,347. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PCDH15Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:55570347
Cytoband: 10q21.1
HGVS: NM_001384140.1(PCDH15):c.4640G>A (p.Gly1547Asp)
Allele change: Missense_G1482D

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.