Variant (rsID / SNP)

rs4786286

rs4786286 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D24. Location: chromosome 16, position 2,552,534. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TBC1D24Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:2552534
Cytoband: 16p13.3
HGVS: NM_001199107.2(TBC1D24):c.*1575C>T
Allele change: Silent

Associated conditions / phenotypes

Familial infantile myoclonic epilepsy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.