Variant (rsID / SNP)
rs4675323
rs4675323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NBEAL1. Location: chromosome 2, position 204,062,061. The table records no clinical significance for this variant.
Reference-table entries
NBEAL1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:204062061
- HGVS
- NM_001378026.1,c.7075A>G,p.Ile2359Val
- Allele change
- Missense_I2330V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.