{{Rsnum
|rsid=748404
|Gene=TGM5
|Chromosome=15
|position=43267033
|Orientation=plus
|GMAF=0.1524
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TGM5
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.6 | 38.7 | 57.7
| HCB | 0.7 | 11.7 | 87.6
| JPT | 0.0 | 12.4 | 87.6
| YRI | 1.4 | 5.4 | 93.2
| ASW | 3.5 | 8.8 | 87.7
| CHB | 0.7 | 11.7 | 87.6
| CHD | 0.0 | 13.8 | 86.2
| GIH | 8.9 | 45.5 | 45.5
| LWK | 0.9 | 20.0 | 79.1
| MEX | 10.3 | 37.9 | 51.7
| MKK | 2.6 | 34.6 | 62.8
| TSI | 3.9 | 42.2 | 53.9
| HapMapRevision=28
}}

In a GWAS dataset of 1,447 [[lung cancer]] cases, and then replicated in another 1300 cases, the [[rs748404]](T) allele was significantly correlated with increased risk (odds ratio 1.15, p = 1.1 × 10e-9), in agreement with a previous meta-analysis.{{PMID|21303977|OA=1
}}

{{PMID Auto
|PMID=19654303
|Title=Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs748404
|overall_frequency_n=22
|overall_frequency_d=128
|overall_frequency=0.171875
|n_genomes=15
|n_genomes_annotated=0
|n_haplomes=16
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}