Variant (rsID / SNP)
rs8091858
rs8091858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AFG3L2. Location: chromosome 18, position 12,358,661. Clinical significance in the table: Benign.
Reference-table entries
AFG3L2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 18:12358661
- Cytoband
- 18p11.21
- HGVS
- NM_006796.3(AFG3L2):c.1026+8G>A
- Allele change
- Silent
Associated conditions / phenotypes
Spinocerebellar ataxia type 28
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.