Variant (rsID / SNP)

rs5744175

rs5744175 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR5. Location: chromosome 1, position 223,284,444. Clinical significance in the table: Benign.

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Reference-table entries

TLR5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:223284444
Cytoband: 1q41
HGVS: NM_003268.6(TLR5):c.1930A>T (p.Ile644Phe)
Allele change: Missense_I644F

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.