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rs5744174

From SNPedia

Orientationminus
Stabilizedminus
Make rs5744174(C;C)
Make rs5744174(C;T)
Make rs5744174(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position223111186
GeneTLR5
is asnp
is mentioned by
dbSNPrs5744174
ebirs5744174
HLIrs5744174
Exacrs5744174
Varsomers5744174
Maprs5744174
PheGenIrs5744174
hapmaprs5744174
1000 genomesrs5744174
hgdprs5744174
ensemblrs5744174
gopubmedrs5744174
geneviewrs5744174
scholarrs5744174
googlers5744174
pharmgkbrs5744174
gwascentralrs5744174
openSNPrs5744174
23andMers5744174
23andMe allrs5744174
SNP Nexus

SNPshotrs5744174
SNPdbers5744174
MSV3drs5744174
GWAS Ctlgrs5744174
GMAF0.2759
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21994405] Genetic Variants of Toll-Like Receptor 2 and 5, Helicobacter pylori Infection, and Risk of Gastric Cancer and Its Precursors in a Chinese Population

[PMID 16846490OA-icon.png] Lemierre's syndrome and genetic polymorphisms: a case report.

[PMID 18325643OA-icon.png] Associations between SNPs in toll-like receptors and related intracellular signaling molecules and immune responses to measles vaccine: preliminary results.

[PMID 18396467OA-icon.png] Genetic variation and haplotype structures of innate immunity genes in eastern India.

[PMID 19505919OA-icon.png] Toll-like receptor signaling pathway variants and prostate cancer mortality.

[PMID 19543401OA-icon.png] Toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women.


GET Evidence
TLR5-F616L
aa_change Phe616Leu
aa_change_short F616L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.333798
summary



[PMID 23593463OA-icon.png] A Non-Synonymous Coding Variant (L616F) in the TLR5 Gene Is Potentially Associated with Crohn's Disease and Influences Responses to Bacterial Flagellin


[PMID 22740716] Toll-like receptor and hepatitis B virus clearance in chronic infected patients: a long-term prospective cohort study in Taiwan.