rs11854949
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11854949(G;G) |
Make rs11854949(G;T) |
Make rs11854949(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 50686144 |
Gene | TRPM7 |
is a | snp |
is | mentioned by |
dbSNP | rs11854949 |
dbSNP (classic) | rs11854949 |
ClinGen | rs11854949 |
ebi | rs11854949 |
HLI | rs11854949 |
Exac | rs11854949 |
Gnomad | rs11854949 |
Varsome | rs11854949 |
LitVar | rs11854949 |
Map | rs11854949 |
PheGenI | rs11854949 |
Biobank | rs11854949 |
1000 genomes | rs11854949 |
hgdp | rs11854949 |
ensembl | rs11854949 |
geneview | rs11854949 |
scholar | rs11854949 |
rs11854949 | |
pharmgkb | rs11854949 |
gwascentral | rs11854949 |
openSNP | rs11854949 |
23andMe | rs11854949 |
SNPshot | rs11854949 |
SNPdbe | rs11854949 |
MSV3d | rs11854949 |
GWAS Ctlg | rs11854949 |
GMAF | 0.07392 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19644062] Gene Variation of the Transient Receptor Potential Cation Channel, Subfamily M, Member 7 (TRPM7), and Risk of Incident Ischemic Stroke. Prospective, Nested, Case-Control Study