Variant (rsID / SNP)

rs61744696

rs61744696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNT1. Location: chromosome 9, position 138,664,762. Clinical significance in the table: Benign.

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Reference-table entries

KCNT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:138664762
Cytoband: 9q34.3
HGVS: NM_020822.3(KCNT1):c.2210C>T (p.Thr737Met)
Allele change: Missense_T737M

Associated conditions / phenotypes

Developmental and epileptic encephalopathy, 14|Autosomal dominant nocturnal frontal lobe epilepsy 5|Seizure|Developmental and epileptic encephalopathy, 14|Autosomal dominant nocturnal frontal lobe epilepsy 5

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.