Variant (rsID / SNP)
rs1667354
rs1667354 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF568. Location: chromosome 19, position 37,482,151. The table records no clinical significance for this variant.
Reference-table entries
ZNF568Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:37482151
- HGVS
- NM_001204838.2,c.479A>G,p.Asp160Gly
- Allele change
- Missense_D96G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.