Variant (rsID / SNP)
rs9908414
rs9908414 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF594. Location: chromosome 17, position 5,087,040. The table records no clinical significance for this variant.
Reference-table entries
ZNF594Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:5087040
- HGVS
- NM_032530.2,c.512T>C,p.Ile171Thr
- Allele change
- Missense_I171T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.