Variant (rsID / SNP)
rs584427
rs584427 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCAM1. Location: chromosome 11, position 113,103,996. The table records no clinical significance for this variant.
Reference-table entries
NCAM1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:113103996
- HGVS
- NM_001400624.1,c.1650T>G,p.Val550Val
- Allele change
- Synonymous_V540V
Associated conditions / phenotypes
Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.