Variant (rsID / SNP)

rs55803460

rs55803460 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKL5. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CDKL5Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xp22.13
HGVS: NM_001323289.2(CDKL5):c.2200A>G (p.Thr734Ala)
Allele change: Missense_T734A

Associated conditions / phenotypes

Developmental and epileptic encephalopathy, 2|Angelman syndrome-like|Developmental and epileptic encephalopathy, 2|CDKL5 disorder

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.