Variant (rsID / SNP)
rs5743700
rs5743700 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR2. Location: chromosome 4, position 154,625,682. The table records no clinical significance for this variant.
Reference-table entries
TLR2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:154625682
- HGVS
- NM_001318787.2,c.1623C>T,p.Phe541Phe
- Allele change
- Synonymous_F541F
Associated conditions / phenotypes
Synonymous_F541F|Synonymous_F541F|Synonymous_F541F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.