Variant (rsID / SNP)

rs3775290

rs3775290 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR3. Location: chromosome 4, position 187,004,217. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TLR3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:187004217
Cytoband: 4q35.1
HGVS: NM_003265.3(TLR3):c.1377C>T (p.Phe459=)
Allele change: Synonymous_F459F

Associated conditions / phenotypes

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.