{{Rsnum
|rsid=1874326
|Gene=TRIM24
|Chromosome=7
|position=138472645
|Orientation=plus
|GMAF=0.2392
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TRIM24
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 25.7 | 71.7
| HCB | 21.2 | 51.8 | 27.0
| JPT | 13.3 | 54.0 | 32.7
| YRI | 2.0 | 25.9 | 72.1
| ASW | 1.9 | 25.9 | 72.2
| CHB | 21.2 | 51.8 | 27.0
| CHD | 26.6 | 55.0 | 18.3
| GIH | 9.9 | 51.5 | 38.6
| LWK | 0.9 | 21.8 | 77.3
| MEX | 6.9 | 36.2 | 56.9
| MKK | 3.2 | 25.6 | 71.2
| TSI | 2.0 | 18.6 | 79.4
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19197348
|Trait=Quantitative traits
|Title=Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
|RiskAllele=G
|Pval=0.000009
|OR=0.22
|ORtxt=[NR] lb. increase
|OA=1
}}

[[Weight]] being the quantitative trait associated with in {{PMID|19197348|OA=1
}}

{{PMID Auto
|PMID=20031603
|Title=A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1874326
|overall_frequency_n=97
|overall_frequency_d=128
|overall_frequency=0.757812
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=88
|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 | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}