Variant (rsID / SNP)
rs3775073
rs3775073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR6. Location: chromosome 4, position 38,829,832. The table records no clinical significance for this variant.
Reference-table entries
TLR6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:38829832
- HGVS
- NM_001394553.1,c.1263A>G,p.Lys421Lys
- Allele change
- Synonymous_K421K
Associated conditions / phenotypes
Endocarditis|Infective Endocarditis|Atherosclerosis Susceptibility|Mycobacterium Tuberculosis 1|Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.