Variant (rsID / SNP)

rs561329680

rs561329680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STXBP1. Location: chromosome 9, position 130,430,371. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

STXBP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:130430371
Cytoband: 9q34.11
HGVS: NM_001032221.6(STXBP1):c.807C>T (p.Ser269=)
Allele change: Synonymous_S269S

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.