Variant (rsID / SNP)
rs2958149
rs2958149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NACA. Location: chromosome 12, position 57,109,792. The table records no clinical significance for this variant.
Reference-table entries
NACANot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:57109792
- HGVS
- NM_001365896.1,c.5522T>C,p.Leu1841Pro
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.