{{Rsnum
|rsid=12279261
|Gene=NCAM1
|Chromosome=11
|position=113235733
|Orientation=plus
|GMAF=0.2158
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NCAM1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 69.0 | 24.8 | 6.2
| HCB | 83.9 | 15.3 | 0.7
| JPT | 76.1 | 23.0 | 0.9
| YRI | 26.5 | 51.0 | 22.4
| ASW | 33.3 | 47.4 | 19.3
| CHB | 83.9 | 15.3 | 0.7
| CHD | 89.0 | 11.0 | 0.0
| GIH | 95.0 | 5.0 | 0.0
| LWK | 26.4 | 50.0 | 23.6
| MEX | 69.0 | 27.6 | 3.4
| MKK | 30.1 | 53.8 | 16.0
| TSI | 59.8 | 32.4 | 7.8
| 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=0.000009
|OR=0.1116
|ORtxt=[NR] unit decrease (main effect)
}}

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