Variant (rsID / SNP)
rs4802965
rs4802965 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF578. Location: chromosome 19, position 53,015,384. The table records no clinical significance for this variant.
Reference-table entries
ZNF578Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:53015384
- HGVS
- NM_001099694.2,c.1750A>G,p.Ile584Val
- Allele change
- Missense_I584V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.