Variant (rsID / SNP)
rs368116
rs368116 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEPTIN9. Location: chromosome 17, position 75,495,775. Clinical significance in the table: Benign.
Reference-table entries
SEPTIN9Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:75495775
- Cytoband
- 17q25.3
- HGVS
- NM_001113491.2(SEPTIN9):c.*1035G>A
- Allele change
- Silent
Associated conditions / phenotypes
Amyotrophic neuralgia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.