Variant (rsID / SNP)

rs79369633

rs79369633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBFOX1. Location: chromosome 16, position 7,759,136. Clinical significance in the table: Benign.

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Reference-table entries

RBFOX1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:7759136
Cytoband: 16p13.3
HGVS: NM_018723.4(RBFOX1):c.1071+3G>A
Allele change: Silent

Associated conditions / phenotypes

Idiopathic generalized epilepsy

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.