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rs7744

From SNPedia

Orientationplus
Stabilizedplus
Make rs7744(A;A)
Make rs7744(A;G)
Make rs7744(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38142530
GeneMYD88
is asnp
is mentioned by
dbSNPrs7744
ebirs7744
HLIrs7744
Exacrs7744
Varsomers7744
Maprs7744
PheGenIrs7744
hapmaprs7744
1000 genomesrs7744
hgdprs7744
ensemblrs7744
gopubmedrs7744
geneviewrs7744
scholarrs7744
googlers7744
pharmgkbrs7744
gwascentralrs7744
openSNPrs7744
23andMers7744
23andMe allrs7744
SNP Nexus

SNPshotrs7744
SNPdbers7744
MSV3drs7744
GWAS Ctlgrs7744
GMAF0.1694
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21525878] A single nucleotide polymorphism in the 3'-untranslated region of MyD88 gene is associated with Buerger disease but not with Takayasu arteritis in Japanese


[PMID 18776126OA-icon.png] Toll-like receptor 9 affects severity of IgA nephropathy.


[PMID 20448286] Association between anti-tumour necrosis factor treatment response and genetic variants within the TLR and NF{kappa}B signalling pathways.


[PMID 20463618OA-icon.png] Role of polymorphic variants as genetic modulators of infection in neonatal sepsis.


[PMID 26959040] SNP-SNP Interaction between TLR4 and MyD88 in Susceptibility to Coronary Artery Disease in the Chinese Han Population.