Variant (rsID / SNP)
rs3744437
rs3744437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBX4. Location: chromosome 17, position 59,561,584. Clinical significance in the table: Benign.
Reference-table entries
TBX4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:59561584
- Cytoband
- 17q23.2
- HGVS
- NM_001321120.2(TBX4):c.*707G>T
- Allele change
- Silent
Associated conditions / phenotypes
Coxopodopatellar syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.