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rs8177400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 3
(G;G) 0 common in complete genomics
Make rs8177400(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position126292695
GeneTIRAP
is asnp
is mentioned by
dbSNPrs8177400
ebirs8177400
HLIrs8177400
Exacrs8177400
Varsomers8177400
Maprs8177400
PheGenIrs8177400
hapmaprs8177400
1000 genomesrs8177400
hgdprs8177400
ensemblrs8177400
gopubmedrs8177400
geneviewrs8177400
scholarrs8177400
googlers8177400
pharmgkbrs8177400
gwascentralrs8177400
openSNPrs8177400
23andMers8177400
23andMe allrs8177400
SNP Nexus

SNPshotrs8177400
SNPdbers8177400
MSV3drs8177400
GWAS Ctlgrs8177400
GMAF0.0005
Max Magnitude3
? (A;A) (A;G) (G;G) 28
[PMID 19509286OA-icon.png] A TIR domain variant of MYD88 adapter-like (MAL)/TIRAP results in loss of MYD88 binding and reduced TLR2/TLR4 signaling


[PMID 20164415] MyD88 Adaptor-Like D96N Is a Naturally Occurring Loss-of-Function Variant of TIRAP

OMIM606252
Desc
Variant
Relatedalso