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