rs11013860
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs11013860(A;A) | 
| Make rs11013860(A;C) | 
| Make rs11013860(C;C) | 
| Reference | GRCh38 38.1/142 | 
| Chromosome | 10 | 
| Position | 18365098 | 
| Gene | CACNB2 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs11013860 | 
| dbSNP (classic) | rs11013860 | 
| ClinGen | rs11013860 | 
| ebi | rs11013860 | 
| HLI | rs11013860 | 
| Exac | rs11013860 | 
| Gnomad | rs11013860 | 
| Varsome | rs11013860 | 
| LitVar | rs11013860 | 
| Map | rs11013860 | 
| PheGenI | rs11013860 | 
| Biobank | rs11013860 | 
| 1000 genomes | rs11013860 | 
| hgdp | rs11013860 | 
| ensembl | rs11013860 | 
| geneview | rs11013860 | 
| scholar | rs11013860 | 
| rs11013860 | |
| pharmgkb | rs11013860 | 
| gwascentral | rs11013860 | 
| openSNP | rs11013860 | 
| 23andMe | rs11013860 | 
| SNPshot | rs11013860 | 
| SNPdbe | rs11013860 | 
| MSV3d | rs11013860 | 
| GWAS Ctlg | rs11013860 | 
| Max Magnitude | 0 | 
| ? | (A;A) (A;C) (C;C) | 28 | 
|---|---|---|
| 
 
 | ||
[PMID 24581832] Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder
Categories: 
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d


