Variant (rsID / SNP)
rs3825663
rs3825663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TDP1. Location: chromosome 14, position 90,429,749. Clinical significance in the table: Benign.
Reference-table entries
TDP1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:90429749
- Cytoband
- 14q32.11
- HGVS
- NM_018319.4(TDP1):c.291A>G (p.Gln97=)
- Allele change
- Synonymous_Q97Q
Associated conditions / phenotypes
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.