Variant (rsID / SNP)
rs4801177
rs4801177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF470. Location: chromosome 19, position 57,089,050. The table records no clinical significance for this variant.
Reference-table entries
ZNF470Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:57089050
- HGVS
- NM_001001668.4,c.1253C>T,p.Thr418Ile
- Allele change
- Missense_T418I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.