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Variant (rsID / SNP)

rs201604887

SCN1A

rs201604887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN1A. Location: chromosome 2, position 166,898,791. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN1AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:166898791
Cytoband
2q24.3
HGVS
NM_001165963.4(SCN1A):c.2176+11A>C
Allele change
Silent

Associated conditions / phenotypes

Migraine, familial hemiplegic, 3|Epilepsy|Generalized epilepsy with febrile seizures plus, type 2|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.