rs312486
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs312486(C;C) |
Make rs312486(C;G) |
Make rs312486(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 53511427 |
Gene | CACNA1D |
is a | snp |
is | mentioned by |
dbSNP | rs312486 |
dbSNP (classic) | rs312486 |
ClinGen | rs312486 |
ebi | rs312486 |
HLI | rs312486 |
Exac | rs312486 |
Gnomad | rs312486 |
Varsome | rs312486 |
LitVar | rs312486 |
Map | rs312486 |
PheGenI | rs312486 |
Biobank | rs312486 |
1000 genomes | rs312486 |
hgdp | rs312486 |
ensembl | rs312486 |
geneview | rs312486 |
scholar | rs312486 |
rs312486 | |
pharmgkb | rs312486 |
gwascentral | rs312486 |
openSNP | rs312486 |
23andMe | rs312486 |
SNPshot | rs312486 |
SNPdbe | rs312486 |
MSV3d | rs312486 |
GWAS Ctlg | rs312486 |
GMAF | 0.1887 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 23229155] The human L-type calcium channel Ca(v)1.3 regulates insulin release and polymorphisms in CACNA1D associate with type 2 diabetes