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TLR6 c.861A>G ;(p.T287=)
Variant ID: 4-38830234-T-C
NM_006068.4(
TLR6
):c.861A>G;(p.T287=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk.
Circulation. Genomic And Precision Medicine
Coassin, Stefan S; Chemello, Kevin K; Khantalin, Ilya I; Forer, Lukas L; Döttelmayer, Patricia P; Schönherr, Sebastian S; Grüneis, Rebecca R; Chong-Hong-Fong, Clément C; Nativel, Brice B; Ramin-Mangata, Stéphane S; Gallo, Antonio A; Roche, Mathias M; Muelegger, Beatrix B; Gieger, Christian C; Peters, Annette A; Zschocke, Johannes J; Marimoutou, Catherine C; Meilhac, Olivier O; Lamina, Claudia C; Kronenberg, Florian F; Blanchard, Valentin V; Lambert, Gilles G
Publication Date: 2022-04
Variant appearance in text: TLR6: Thr287Thr; rs5743812
PubMed Link:
35133173
Variant Present in the following documents:
hcg-15-e003489-s001.pdf
View BVdb publication page
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Bmc Medical Genetics
Henmyr, V V; Carlberg, D D; Manderstedt, E E; Lind-Halldén, C C; Säll, T T; Cardell, L O LO; Halldén, C C
Publication Date: 2017-02-23
Variant appearance in text: TLR6: T287T; rs5743812
PubMed Link:
28228119
Variant Present in the following documents:
12881_2017_379_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page