Variant (rsID / SNP)
rs79736939
rs79736939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCTD7. Location: chromosome 7, position 66,104,927. Clinical significance in the table: Benign.
Reference-table entries
KCTD7Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:66104927
- Cytoband
- 7q11.21
- HGVS
- NM_153033.5(KCTD7):c.*708C>T
- Allele change
- Silent
Associated conditions / phenotypes
Progressive myoclonic epilepsy type 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.