Variant (rsID / SNP)
rs2235648
rs2235648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUBP2. Location: chromosome 16, position 1,836,796. The table records no clinical significance for this variant.
Reference-table entries
NUBP2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:1836796
- HGVS
- NM_012225.4,c.174C>A,p.Ile58Ile
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.