Gene entry
ANO10
anoctamin 10
- Chromosome
- 3
- Cytoband
- 3p22.1-p21.33
- Variants (rsID)
- 44
ANO10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.1-p21.33). Its official name is “anoctamin 10”. The reference table lists 44 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs17409162Benignsingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
- rs56389778Benignsingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
- rs61732728Conflicting interpretationssingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
- rs138000380Uncertain significancesingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
- rs144272231Uncertain significancesingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
- rs188443010Uncertain significancesingle nucleotide variantAutosomal recessive spinocerebellar ataxia 10
Other listed variants
- rs965928
- rs3772160
- rs4432612
- rs4462942
- rs4547674
- rs4682900
- rs6782070
- rs9856765
- rs9874278
- rs13076840
- rs13319228
- rs17075704
- rs17075841
- rs35794830
- rs41289586
- rs62250916
- rs62253028
- rs72622910
- rs73081016
- rs73083006
- rs76599417
- rs78071591
- rs78549154
- rs114623053
- rs115304875
- rs116857315
- rs117380106
- rs139364152
- rs141320140
- rs142841719
- rs144049014
- rs145068762
- rs147605535
- rs149298412
- rs184756780
- rs185862313
- rs201052710
- rs201719088
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.