Variant (rsID / SNP)

rs4986791

rs4986791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR4. Location: chromosome 9, position 120,475,602. Clinical significance in the table: Benign.

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Reference-table entries

TLR4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:120475602
Cytoband: 9q33.1
HGVS: NM_138554.5(TLR4):c.1196C>T (p.Thr399Ile)
Allele change: Missense_T359I

Associated conditions / phenotypes

TLR4 POLYMORPHISM

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.