rs11614912
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11614912(A;A) |
Make rs11614912(A;G) |
Make rs11614912(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 6039389 |
Gene | VWF |
is a | snp |
is | mentioned by |
dbSNP | rs11614912 |
dbSNP (classic) | rs11614912 |
ClinGen | rs11614912 |
ebi | rs11614912 |
HLI | rs11614912 |
Exac | rs11614912 |
Gnomad | rs11614912 |
Varsome | rs11614912 |
LitVar | rs11614912 |
Map | rs11614912 |
PheGenI | rs11614912 |
Biobank | rs11614912 |
1000 genomes | rs11614912 |
hgdp | rs11614912 |
ensembl | rs11614912 |
geneview | rs11614912 |
scholar | rs11614912 |
rs11614912 | |
pharmgkb | rs11614912 |
gwascentral | rs11614912 |
openSNP | rs11614912 |
23andMe | rs11614912 |
SNPshot | rs11614912 |
SNPdbe | rs11614912 |
MSV3d | rs11614912 |
GWAS Ctlg | rs11614912 |
GMAF | 0.1244 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 23143626] Hsa-miR-196a2 Functional SNP is Associated With Severe Toxicity After Platinum-Based Chemotherapy of Advanced Nonsmall Cell Lung Cancer Patients in a Chinese Population
[PMID 20346360] Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.