Variant (rsID / SNP)
rs1269621
rs1269621 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRCAM. Location: chromosome 7, position 107,849,908. The table records no clinical significance for this variant.
Reference-table entries
NRCAMNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:107849908
- HGVS
- NM_001371156.1,c.1032C>T,p.Asn344Asn
- Allele change
- Synonymous_N338N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.