Variant (rsID / SNP)

rs771862017

rs771862017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTAN1. Location: chromosome 9, position 131,367,755. Clinical significance in the table: Likely benign.

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Reference-table entries

SPTAN1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:131367755
Cytoband: 9q34.11
HGVS: NM_001130438.3(SPTAN1):c.4045C>T (p.Arg1349Trp)
Allele change: Silent

Associated conditions / phenotypes

Early infantile epileptic encephalopathy with suppression bursts

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.