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Variant (rsID / SNP)

rs5744168

TLR5

rs5744168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR5. Location: chromosome 1, position 223,285,200. Clinical significance in the table: protective; risk factor.

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Reference-table entries

TLR5Risk factor
Clinical significance (as recorded)
protective; risk factor
Variant type
single nucleotide variant
Chromosome / position
1:223285200
Cytoband
1q41
HGVS
NM_003268.6(TLR5):c.1174C>T (p.Arg392Ter)
Allele change
Nonsense_R392X

Associated conditions / phenotypes

Legionnaire disease, susceptibility to|Systemic lupus erythematosus, resistance to, 1|Melioidosis, resistance to

Public references

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