Variant (rsID / SNP)
rs4986790
rs4986790 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR4. Location: chromosome 9, position 120,475,302. Clinical significance in the table: Benign; protective.
Reference-table entries
TLR4Benign
- Clinical significance (as recorded)
- Benign; protective
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:120475302
- Cytoband
- 9q33.1
- HGVS
- NM_138554.5(TLR4):c.896A>G (p.Asp299Gly)
- Allele change
- Missense_D259G
Associated conditions / phenotypes
TLR4 POLYMORPHISM|Pericementitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.