Variant (rsID / SNP)
rs117337557
rs117337557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A2. Location: chromosome 1, position 40,768,191. Clinical significance in the table: Likely benign.
Reference-table entries
COL9A2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:40768191
- Cytoband
- 1p34.2
- HGVS
- NM_001852.4(COL9A2):c.1792+102C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.