rs17061085
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17061085(A;A) |
Make rs17061085(A;G) |
Make rs17061085(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 59705999 |
Gene | LOC105377110 |
is a | snp |
is | mentioned by |
dbSNP | rs17061085 |
dbSNP (classic) | rs17061085 |
ClinGen | rs17061085 |
ebi | rs17061085 |
HLI | rs17061085 |
Exac | rs17061085 |
Gnomad | rs17061085 |
Varsome | rs17061085 |
LitVar | rs17061085 |
Map | rs17061085 |
PheGenI | rs17061085 |
Biobank | rs17061085 |
1000 genomes | rs17061085 |
hgdp | rs17061085 |
ensembl | rs17061085 |
geneview | rs17061085 |
scholar | rs17061085 |
rs17061085 | |
pharmgkb | rs17061085 |
gwascentral | rs17061085 |
openSNP | rs17061085 |
23andMe | rs17061085 |
SNPshot | rs17061085 |
SNPdbe | rs17061085 |
MSV3d | rs17061085 |
GWAS Ctlg | rs17061085 |
GMAF | 0.09642 |
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