Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4823561

CELSR1

rs4823561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELSR1. Location: chromosome 22, position 46,929,692. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CELSR1Not classified
Variant type
missense_variant
Chromosome / position
22:46929692
HGVS
NM_001378328.1,c.3376T>C,p.Cys1126Arg
Allele change
Missense_C1126R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.