Variant (rsID / SNP)
rs4823850
rs4823850 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELSR1. Location: chromosome 22, position 46,931,077. The table records no clinical significance for this variant.
Reference-table entries
CELSR1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:46931077
- HGVS
- NM_001378328.1,c.1991C>G,p.Ser664Trp
- Allele change
- Missense_S664W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.