Variant (rsID / SNP)
rs913588
rs913588 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDM4C. Location: chromosome 9, position 7,174,673. The table records no clinical significance for this variant.
Reference-table entries
KDM4CNot classified
- Variant type
- missense_variant
- Chromosome / position
- 9:7174673
- HGVS
- NM_001353997.3,c.3214G>A,p.Val1072Ile
- Allele change
- Silent
Associated conditions / phenotypes
Missense_V1072I|Silent|Missense_V1039I|Missense_V784I|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.