Variant (rsID / SNP)

rs150315296

rs150315296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR3. Location: chromosome 4, position 187,004,768. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TLR3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:187004768
Cytoband: 4q35.1
HGVS: NM_003265.3(TLR3):c.1928G>A (p.Arg643His)
Allele change: Missense_R643H

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.