rs10848635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10848635(A;A) |
Make rs10848635(A;T) |
Make rs10848635(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 2207029 |
Gene | CACNA1C |
is a | snp |
is | mentioned by |
dbSNP | rs10848635 |
dbSNP (classic) | rs10848635 |
ClinGen | rs10848635 |
ebi | rs10848635 |
HLI | rs10848635 |
Exac | rs10848635 |
Gnomad | rs10848635 |
Varsome | rs10848635 |
LitVar | rs10848635 |
Map | rs10848635 |
PheGenI | rs10848635 |
Biobank | rs10848635 |
1000 genomes | rs10848635 |
hgdp | rs10848635 |
ensembl | rs10848635 |
geneview | rs10848635 |
scholar | rs10848635 |
rs10848635 | |
pharmgkb | rs10848635 |
gwascentral | rs10848635 |
openSNP | rs10848635 |
23andMe | rs10848635 |
SNPshot | rs10848635 |
SNPdbe | rs10848635 |
MSV3d | rs10848635 |
GWAS Ctlg | rs10848635 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 24581832] Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder