Variant (rsID / SNP)
rs1033325
rs1033325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCNX2. Location: chromosome 1, position 233,398,713. The table records no clinical significance for this variant.
Reference-table entries
PCNX2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:233398713
- HGVS
- NM_014801.4,c.350G>A,p.Arg117Lys
- Allele change
- Missense_R117K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.