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rs9925481

From SNPedia

Orientationplus
Stabilizedplus
Make rs9925481(C;C)
Make rs9925481(C;T)
Make rs9925481(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11003622
GeneCLEC16A
is asnp
is mentioned by
dbSNPrs9925481
ebirs9925481
HLIrs9925481
Exacrs9925481
Varsomers9925481
Maprs9925481
PheGenIrs9925481
hapmaprs9925481
1000 genomesrs9925481
hgdprs9925481
ensemblrs9925481
gopubmedrs9925481
geneviewrs9925481
scholarrs9925481
googlers9925481
pharmgkbrs9925481
gwascentralrs9925481
openSNPrs9925481
23andMers9925481
23andMe allrs9925481
SNP Nexus

SNPshotrs9925481
SNPdbers9925481
MSV3drs9925481
GWAS Ctlgrs9925481
GMAF0.1162
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19787205] Association of genetic variants with myocardial infarction in individuals with or without hypertension or diabetes mellitus


[PMID 20036365] Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals

[PMID 20043139] Association of genetic variants with ischemic stroke in Japanese individuals with or without metabolic syndrome


[PMID 20372818] Genetic risk for myocardial infarction in Japanese individuals with or without chronic kidney disease