Variant (rsID / SNP)
rs1635560
rs1635560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL2A1. Location: chromosome 12, position 48,367,829. Clinical significance in the table: Benign.
Reference-table entries
COL2A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:48367829
- Cytoband
- 12q13.11
- HGVS
- NM_001844.5(COL2A1):c.4317+43C>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.