{{Rsnum
|rsid=2298948
|Gene=GCFC2
|Chromosome=2
|position=75699439
|Orientation=minus
|GMAF=0.2764
|Gene_s=GCFC2
|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 | 43.4 | 46.9 | 9.7
| HCB | 35.0 | 47.4 | 17.5
| JPT | 27.4 | 54.0 | 18.6
| YRI | 88.4 | 10.9 | 0.7
| ASW | 89.5 | 10.5 | 0.0
| CHB | 35.0 | 47.4 | 17.5
| CHD | 40.4 | 42.2 | 17.4
| GIH | 48.5 | 38.6 | 12.9
| LWK | 83.6 | 15.5 | 0.9
| MEX | 39.7 | 50.0 | 10.3
| MKK | 82.1 | 16.7 | 1.3
| TSI | 48.0 | 39.2 | 12.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22745009
|Trait=None
|Title=Multiple loci influencing hippocampal degeneration identified by genome scan.
|RiskAllele=C
|Pval=5E-8
|OR=None
|ORtxt=None
|OA=1
}}

{{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}}