Variant (rsID / SNP)
rs10998973
rs10998973 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL13A1. Location: chromosome 10, position 71,562,437. The table records no clinical significance for this variant.
Reference-table entries
COL13A1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:71562437
- HGVS
- NM_001368882.1,c.258G>A,p.Thr86Thr
- Allele change
- Synonymous_T86T
Associated conditions / phenotypes
Synonymous_T86T|Synonymous_T86T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.