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Variant (rsID / SNP)

rs770187706

KCNQ2

rs770187706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNQ2. Location: chromosome 20, position 62,073,801. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNQ2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
20:62073801
Cytoband
20q13.33
HGVS
NM_172107.4(KCNQ2):c.774C>T (p.Asn258=)
Allele change
Synonymous_N258N

Associated conditions / phenotypes

Seizure|Early infantile epileptic encephalopathy with suppression bursts

Public references

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