Variant (rsID / SNP)

rs1437824

rs1437824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ3. Location: chromosome 8, position 133,136,551. Clinical significance in the table: Benign.

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Reference-table entries

KCNQ3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:133136551
Cytoband: 8q24.22
HGVS: NM_004519.4(KCNQ3):c.*4958A>G
Allele change: Silent

Associated conditions / phenotypes

Seizures, benign familial neonatal, 2|Benign neonatal seizures

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.