Variant (rsID / SNP)
rs115558182
rs115558182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL11A1. Location: chromosome 1, position 103,573,491. Clinical significance in the table: Benign.
Reference-table entries
COL11A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:103573491
- Cytoband
- 1p21.1
- HGVS
- NM_001854.4(COL11A1):c.106+138T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.