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rs11614912

From SNPedia

Orientationplus
Stabilizedplus
Make rs11614912(A;A)
Make rs11614912(A;G)
Make rs11614912(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6039389
GeneVWF
is asnp
is mentioned by
dbSNPrs11614912
ebirs11614912
HLIrs11614912
Exacrs11614912
Varsomers11614912
Maprs11614912
PheGenIrs11614912
hapmaprs11614912
1000 genomesrs11614912
hgdprs11614912
ensemblrs11614912
gopubmedrs11614912
geneviewrs11614912
scholarrs11614912
googlers11614912
pharmgkbrs11614912
gwascentralrs11614912
openSNPrs11614912
23andMers11614912
23andMe allrs11614912
SNP Nexus

SNPshotrs11614912
SNPdbers11614912
MSV3drs11614912
GWAS Ctlgrs11614912
GMAF0.1244
Max Magnitude
? (A;A) (A;G) (G;G) 28

[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 20346360OA-icon.png] Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.