{{Rsnum
|rsid=749005
|Gene=F13A1
|Chromosome=6
|position=6283433
|Orientation=minus
|GMAF=0.1373
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=F13A1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 3.5 | 25.7 | 70.8
| HCB | 0.0 | 3.7 | 96.3
| JPT | 0.0 | 11.5 | 88.5
| YRI | 1.4 | 29.9 | 68.7
| ASW | 1.8 | 35.1 | 63.2
| CHB | 0.0 | 3.7 | 96.3
| CHD | 0.0 | 4.6 | 95.4
| GIH | 0.0 | 13.9 | 86.1
| LWK | 3.7 | 22.0 | 74.3
| MEX | 3.4 | 44.8 | 51.7
| MKK | 5.8 | 32.7 | 61.5
| TSI | 4.9 | 35.3 | 59.8
| 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=3E-7
|OR=0.0002
|ORtxt=[NR] unit decrease (main effect)
}}

{{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}}