Variant (rsID / SNP)
rs4493966
rs4493966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TJP2. Location: chromosome 9, position 71,820,148. Clinical significance in the table: Benign.
Reference-table entries
TJP2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:71820148
- Cytoband
- 9q21.11
- HGVS
- NM_004817.4(TJP2):c.61-7316G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.