Variant (rsID / SNP)
rs3732782
rs3732782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF80. Location: chromosome 3, position 113,955,164. The table records no clinical significance for this variant.
Reference-table entries
ZNF80Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:113955164
- HGVS
- NM_007136.4,c.758A>C,p.Asp253Ala
- Allele change
- Missense_D253A
Associated conditions / phenotypes
Tardive Dyskinesia|Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.