Gene entry
SEPTIN9
septin 9
- Chromosome
- 17
- Cytoband
- 17q25.3
- Variants (rsID)
- 70
SEPTIN9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.3). Its official name is “septin 9”. The reference table lists 70 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs1059485Benignsingle nucleotide variantAmyotrophic neuralgia
- rs34587622Benignsingle nucleotide variantAmyotrophic neuralgia
- rs368116Benignsingle nucleotide variantAmyotrophic neuralgia
- rs448203Benignsingle nucleotide variantAmyotrophic neuralgia
- rs73377525Benignsingle nucleotide variantAmyotrophic neuralgia
- rs425139Not classifiedintron_variant
Other listed variants
- rs93075
- rs312801
- rs312818
- rs312820
- rs312853
- rs312882
- rs312891
- rs312892
- rs312893
- rs312903
- rs379902
- rs388090
- rs416438
- rs417734
- rs873370
- rs1715491
- rs1995755
- rs2898645
- rs3760143
- rs4239000
- rs4788985
- rs4789448
- rs4789455
- rs4789492
- rs8065977
- rs8079187
- rs11077899
- rs12452771
- rs12601624
- rs12943240
- rs35546945
- rs35553148
- rs35971812
- rs62077376
- rs62077400
- rs67415822
- rs72880519
- rs72887155
- rs72887165
- rs72887176
- rs72896159
- rs72896181
- rs73371430
- rs74702026
- rs74894972
- rs75241607
- rs77257328
- rs77357836
- rs77653632
- rs78539590
- rs78614029
- rs78625380
- rs79577179
- rs80097365
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.