Variant (rsID / SNP)
rs16921260
rs16921260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDM4E. Location: chromosome 11, position 94,759,494. The table records no clinical significance for this variant.
Reference-table entries
KDM4ENot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:94759494
- HGVS
- NM_001161630.1,c.773T>C,p.Phe258Ser
- Allele change
- Missense_F258S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.