Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs754910706

SPTAN1

rs754910706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTAN1. Location: chromosome 9, position 131,388,191. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SPTAN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:131388191
Cytoband
9q34.11
HGVS
NM_001130438.3(SPTAN1):c.6213C>G (p.Ser2071Arg)
Allele change
Silent

Associated conditions / phenotypes

Early infantile epileptic encephalopathy with suppression bursts|Developmental and epileptic encephalopathy, 5

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.