rs11226029
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11226029(A;A) |
Make rs11226029(A;G) |
Make rs11226029(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 103822899 |
is a | snp |
is | mentioned by |
dbSNP | rs11226029 |
dbSNP (classic) | rs11226029 |
ClinGen | rs11226029 |
ebi | rs11226029 |
HLI | rs11226029 |
Exac | rs11226029 |
Gnomad | rs11226029 |
Varsome | rs11226029 |
LitVar | rs11226029 |
Map | rs11226029 |
PheGenI | rs11226029 |
Biobank | rs11226029 |
1000 genomes | rs11226029 |
hgdp | rs11226029 |
ensembl | rs11226029 |
geneview | rs11226029 |
scholar | rs11226029 |
rs11226029 | |
pharmgkb | rs11226029 |
gwascentral | rs11226029 |
openSNP | rs11226029 |
23andMe | rs11226029 |
SNPshot | rs11226029 |
SNPdbe | rs11226029 |
MSV3d | rs11226029 |
GWAS Ctlg | rs11226029 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Named in 10.1056/NEJMoa1605086 as a SNP potentially used in the calculation of a cardiovascular genetic risk score