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Variant (rsID / SNP)

rs35311343

TLR3

rs35311343 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR3. Location: chromosome 4, position 187,003,729. Clinical significance in the table: Likely benign.

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Reference-table entries

TLR3Likely benign
Clinical significance (as recorded)
Likely benign
Variant type
single nucleotide variant
Chromosome / position
4:187003729
Cytoband
4q35.1
HGVS
NM_003265.3(TLR3):c.889C>G (p.Leu297Val)
Allele change
Missense_L297V

Associated conditions / phenotypes

Herpes simplex encephalitis, susceptibility to, 2|Herpes simplex encephalitis, susceptibility to, 1|Multisystem inflammatory syndrome in children

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.