Variant (rsID / SNP)
rs227003
rs227003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAJ13. Location: chromosome 14, position 23,000,062. The table records no clinical significance for this variant.
Reference-table entries
TRAJ13Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 14:23000062
- HGVS
- unassigned_transcript_2249,c.37T>C,p.Leu13Leu
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.