Variant (rsID / SNP)
rs149690829
rs149690829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A3. Location: chromosome 20, position 61,452,556. Clinical significance in the table: Likely benign.
Reference-table entries
COL9A3Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:61452556
- Cytoband
- 20q13.33
- HGVS
- NM_001853.4(COL9A3):c.333G>A (p.Pro111=)
- Allele change
- Synonymous_P111P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.