rs11105306
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11105306(C;C) |
Make rs11105306(C;T) |
Make rs11105306(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 89503611 |
Gene | POC1B |
is a | snp |
is | mentioned by |
dbSNP | rs11105306 |
dbSNP (classic) | rs11105306 |
ClinGen | rs11105306 |
ebi | rs11105306 |
HLI | rs11105306 |
Exac | rs11105306 |
Gnomad | rs11105306 |
Varsome | rs11105306 |
LitVar | rs11105306 |
Map | rs11105306 |
PheGenI | rs11105306 |
Biobank | rs11105306 |
1000 genomes | rs11105306 |
hgdp | rs11105306 |
ensembl | rs11105306 |
geneview | rs11105306 |
scholar | rs11105306 |
rs11105306 | |
pharmgkb | rs11105306 |
gwascentral | rs11105306 |
openSNP | rs11105306 |
23andMe | rs11105306 |
SNPshot | rs11105306 |
SNPdbe | rs11105306 |
MSV3d | rs11105306 |
GWAS Ctlg | rs11105306 |
Max Magnitude | 0 |
[PMID 26908625] Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.