Variant (rsID / SNP)
rs36203374
rs36203374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBX3. Location: chromosome 12, position 115,121,732. Clinical significance in the table: Benign.
Reference-table entries
TBX3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:115121732
- Cytoband
- 12q24.21
- HGVS
- NM_005996.4(TBX3):c.-727T>C
- Allele change
- Silent
Associated conditions / phenotypes
Ulnar-mammary syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.