Variant (rsID / SNP)

rs3775291

rs3775291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR3. Location: chromosome 4, position 187,004,074. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TLR3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:187004074
Cytoband: 4q35.1
HGVS: NM_003265.3(TLR3):c.1234C>T (p.Leu412Phe)
Allele change: Missense_L412F

Associated conditions / phenotypes

Susceptibility to HIV infection|Herpes simplex encephalitis, susceptibility to, 2|Herpes simplex encephalitis, susceptibility to, 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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