Variant (rsID / SNP)
rs11543348
rs11543348 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYNC2I2, SPTAN1. Location: chromosome 9, position 131,395,768. Clinical significance in the table: Likely benign.
Reference-table entries
DYNC2I2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:131395768
- Cytoband
- 9q34.11
- HGVS
- NM_001130438.3(SPTAN1):c.*155G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.