Variant (rsID / SNP)
rs3804099
rs3804099 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR2. Location: chromosome 4, position 154,624,656. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 4:154624656
- HGVS
- NM_001318787.2,c.597T>C,p.Asn199Asn
- Allele change
- Synonymous_N199N
Associated conditions / phenotypes
Helicobacter Pylori Infection|Pulmonary Tuberculosis|Peptic Ulcer Disease|Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets|Female Breast Cancer|Polycystic Ovary Syndrome|Tuberculous Meningitis|Mycobacterium Tuberculosis 1|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder|Cytokine Deficiency|Autoimmune Disease|Colorectal Cancer|Gastritis|Psoriasis 1|Osteomyelitis|Inflammatory Bowel Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.