rs7174839
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7174839(C;C) |
Make rs7174839(C;G) |
Make rs7174839(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 50597427 |
Gene | TRPM7 |
is a | snp |
is | mentioned by |
dbSNP | rs7174839 |
dbSNP (classic) | rs7174839 |
ClinGen | rs7174839 |
ebi | rs7174839 |
HLI | rs7174839 |
Exac | rs7174839 |
Gnomad | rs7174839 |
Varsome | rs7174839 |
LitVar | rs7174839 |
Map | rs7174839 |
PheGenI | rs7174839 |
Biobank | rs7174839 |
1000 genomes | rs7174839 |
hgdp | rs7174839 |
ensembl | rs7174839 |
geneview | rs7174839 |
scholar | rs7174839 |
rs7174839 | |
pharmgkb | rs7174839 |
gwascentral | rs7174839 |
openSNP | rs7174839 |
23andMe | rs7174839 |
SNPshot | rs7174839 |
SNPdbe | rs7174839 |
MSV3d | rs7174839 |
GWAS Ctlg | rs7174839 |
GMAF | 0.4835 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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