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Variant (rsID / SNP)

rs374452942

SCN8A

rs374452942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN8A. Location: chromosome 12, position 52,159,580. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN8AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:52159580
Cytoband
12q13.13
HGVS
NM_001330260.2(SCN8A):c.2670C>T (p.Ala890=)
Allele change
Synonymous_A890A

Associated conditions / phenotypes

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.