Variant (rsID / SNP)
rs2293730
rs2293730 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAV27. Location: chromosome 14, position 22,616,547. The table records no clinical significance for this variant.
Reference-table entries
TRAV27Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 14:22616547
- HGVS
- unassigned_transcript_2174,c.288A>G,p.Ala96Ala
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.