{{Rsnum
|rsid=990324
|Gene=LINC00423
|Chromosome=13
|position=32813108
|Orientation=plus
|GMAF=0.1699
|Gene_s=LINC00423
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 83.2 | 15.9 | 0.9
| HCB | 92.7 | 7.3 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 23.8 | 51.0 | 25.2
| ASW | 29.8 | 56.1 | 14.0
| CHB | 92.7 | 7.3 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 78.2 | 20.8 | 1.0
| LWK | 26.4 | 50.0 | 23.6
| MEX | 75.9 | 20.7 | 3.4
| MKK | 35.9 | 48.1 | 16.0
| TSI | 76.5 | 20.6 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21116278
|Trait=None
|Title=Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
|RiskAllele=
|Pval=0.000005
|OR=0.0064
|ORtxt=[NR] unit decrease (interaction)
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}