rs17691914
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17691914(A;A) |
Make rs17691914(A;G) |
Make rs17691914(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 34921311 |
Gene | LOC101928135 |
is a | snp |
is | mentioned by |
dbSNP | rs17691914 |
dbSNP (classic) | rs17691914 |
ClinGen | rs17691914 |
ebi | rs17691914 |
HLI | rs17691914 |
Exac | rs17691914 |
Gnomad | rs17691914 |
Varsome | rs17691914 |
LitVar | rs17691914 |
Map | rs17691914 |
PheGenI | rs17691914 |
Biobank | rs17691914 |
1000 genomes | rs17691914 |
hgdp | rs17691914 |
ensembl | rs17691914 |
geneview | rs17691914 |
scholar | rs17691914 |
rs17691914 | |
pharmgkb | rs17691914 |
gwascentral | rs17691914 |
openSNP | rs17691914 |
23andMe | rs17691914 |
SNPshot | rs17691914 |
SNPdbe | rs17691914 |
MSV3d | rs17691914 |
GWAS Ctlg | rs17691914 |
GMAF | 0.06749 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 21980348] Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery