rs8177400
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 3 | |
| (G;G) | 0 | common in complete genomics |
| Make rs8177400(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 126292695 |
| Gene | TIRAP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8177400 |
| dbSNP (classic) | rs8177400 |
| ClinGen | rs8177400 |
| ebi | rs8177400 |
| HLI | rs8177400 |
| Exac | rs8177400 |
| Gnomad | rs8177400 |
| Varsome | rs8177400 |
| LitVar | rs8177400 |
| Map | rs8177400 |
| PheGenI | rs8177400 |
| Biobank | rs8177400 |
| 1000 genomes | rs8177400 |
| hgdp | rs8177400 |
| ensembl | rs8177400 |
| geneview | rs8177400 |
| scholar | rs8177400 |
| rs8177400 | |
| pharmgkb | rs8177400 |
| gwascentral | rs8177400 |
| openSNP | rs8177400 |
| 23andMe | rs8177400 |
| SNPshot | rs8177400 |
| SNPdbe | rs8177400 |
| MSV3d | rs8177400 |
| GWAS Ctlg | rs8177400 |
| GMAF | 0.0005 |
| Max Magnitude | 3 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19509286
] 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
