{{Rsnum
|rsid=4948418
|Gene=ANK3
|Chromosome=10
|position=62185494
|Orientation=plus
|GMAF=0.1341
|Gene_s=ANK3
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 83.2 | 16.8 | 0.0
| HCB | 65.4 | 29.4 | 5.1
| JPT | 40.7 | 47.8 | 11.5
| YRI | 100.0 | 0.0 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 65.4 | 29.4 | 5.1
| CHD | 60.6 | 36.7 | 2.8
| GIH | 72.3 | 23.8 | 4.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 50.0 | 36.2 | 13.8
| MKK | 94.2 | 5.8 | 0.0
| TSI | 88.2 | 11.8 | 0.0
| HapMapRevision=28
}}[http://blog.23andme.com/2008/08/18/snpwatch-snps-in-ion-channel-genes-are-associated-with-type-2-diabetes-and-bipolar-disorder/ 23andMe blog] ({{PMID|18711365|OA=1
}}) [[rs10994336]] or ([[rs4948418]]) Each T at this SNP increased the odds of developing [[bipolar disorder]] by 1.45 times compared to the CC genotype.

{{PMID Auto GWAS
|PMID=22182935
|Trait=None
|Title=Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
|RiskAllele=T
|Pval=4E-10
|OR=None
|ORtxt=None
}}

{{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}}