Variant (rsID / SNP)
rs2294024
rs2294024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TG. Location: chromosome 8, position 134,144,113. Clinical significance in the table: Benign.
Reference-table entries
TGBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:134144113
- Cytoband
- 8q24.22
- HGVS
- NM_003235.5(TG):c.7920C>T (p.Tyr2640=)
- Allele change
- Synonymous_Y2640Y
Associated conditions / phenotypes
Iodotyrosyl coupling defect
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.