Gene entry
RBFOX1
RNA binding fox-1 homolog 1
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 1,083
RBFOX1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “RNA binding fox-1 homolog 1”. The reference table lists 1083 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs113298071Benignsingle nucleotide variantIdiopathic generalized epilepsy
- rs79369633Benignsingle nucleotide variantIdiopathic generalized epilepsy
- rs151214012Likely benignsingle nucleotide variantIdiopathic generalized epilepsy
Other listed variants
- rs42492
- rs43141
- rs482896
- rs485335
- rs487464
- rs509164
- rs514346
- rs524181
- rs526368
- rs536727
- rs545134
- rs550895
- rs572806
- rs582567
- rs653127
- rs676143
- rs729172
- rs729533
- rs740057
- rs741168
- rs756411
- rs757604
- rs758449
- rs758491
- rs763650
- rs767888
- rs801996
- rs809684
- rs813913
- rs813914
- rs867163
- rs870288
- rs889701
- rs899312
- rs935810
- rs956818
- rs963557
- rs964308
- rs970060
- rs985992
- rs1000192
- rs1008353
- rs1011489
- rs1013615
- rs1014127
- rs1016175
- rs1019190
- rs1019253
- rs1024696
- rs1034988
- rs1035564
- rs1105004
- rs1345887
- rs1358489
- rs1362315
- rs1382478
- rs1382480
- rs1418265
- rs1424133
- rs1436116
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.