{{Rsnum
|rsid=1795648
|Gene=ERC2
|Chromosome=3
|position=55537732
|Orientation=plus
|GMAF=0.3228
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ERC2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 53.1 | 39.8 | 7.1
| HCB | 66.4 | 27.7 | 5.8
| JPT | 61.1 | 36.3 | 2.7
| YRI | 17.7 | 43.5 | 38.8
| ASW | 15.8 | 57.9 | 26.3
| CHB | 66.4 | 27.7 | 5.8
| CHD | 69.7 | 26.6 | 3.7
| GIH | 59.4 | 35.6 | 5.0
| LWK | 12.1 | 45.8 | 42.1
| MEX | 44.8 | 46.6 | 8.6
| MKK | 0.0 | 0.0 | 0.0
| TSI | 49.0 | 43.1 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21057379
|Trait=None
|Title=Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
|RiskAllele=
|Pval=0.000006
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}