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rs7893395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7893395(C;T)
Make rs7893395(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position16863501
GeneCUBN
is asnp
is mentioned by
dbSNPrs7893395
ebirs7893395
HLIrs7893395
Exacrs7893395
Varsomers7893395
Maprs7893395
PheGenIrs7893395
hapmaprs7893395
1000 genomesrs7893395
hgdprs7893395
ensemblrs7893395
gopubmedrs7893395
geneviewrs7893395
scholarrs7893395
googlers7893395
pharmgkbrs7893395
gwascentralrs7893395
openSNPrs7893395
23andMers7893395
23andMe allrs7893395
SNP Nexus

SNPshotrs7893395
SNPdbers7893395
MSV3drs7893395
GWAS Ctlgrs7893395
GMAF0.3242
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20855565OA-icon.png] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease