Variant (rsID / SNP)

rs141980692

rs141980692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTAN1. Location: chromosome 9, position 131,395,498. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SPTAN1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:131395498
Cytoband: 9q34.11
HGVS: NM_001130438.3(SPTAN1):c.7319G>A (p.Arg2440Gln)
Allele change: Silent

Associated conditions / phenotypes

Early infantile epileptic encephalopathy with suppression bursts|Developmental and epileptic encephalopathy, 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.