{{Rsnum
|rsid=8177400
|Gene=TIRAP
|Chromosome=11
|position=126292695
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.0005
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TIRAP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 1.8 | 98.2
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19509286
|Title=A TIR domain variant of MYD88 adapter-like (MAL)/TIRAP results in loss of MYD88 binding and reduced TLR2/TLR4 signaling
|OA=1
}}

{{PMID Auto
|PMID=20164415
|Title=MyD88 Adaptor-Like D96N Is a Naturally Occurring Loss-of-Function Variant of TIRAP
}}

{{omim
|id=606252
|rsnum=8177400
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}