Variant (rsID / SNP)
rs415304
rs415304 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HELZ2. Location: chromosome 20, position 62,198,236. The table records no clinical significance for this variant.
Reference-table entries
HELZ2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:62198236
- HGVS
- NM_001037335.2,c.2475C>T,p.Arg825Arg
- Allele change
- Synonymous_R256R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.