Variant (rsID / SNP)
rs12963422
rs12963422 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPK2. Location: chromosome 18, position 56,204,644. The table records no clinical significance for this variant.
Reference-table entries
ALPK2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:56204644
- HGVS
- NM_052947.4,c.2775A>C,p.Val925Val
- Allele change
- Synonymous_V925V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.