Variant (rsID / SNP)
rs7105734
rs7105734 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCAM1. Location: chromosome 11, position 112,832,353. The table records no clinical significance for this variant.
Reference-table entries
NCAM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:112832353
- HGVS
- NM_001400624.1,c.19T>C,p.Phe7Leu
- Allele change
- Silent
Associated conditions / phenotypes
Missense_F7L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.