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rs9268402

From SNPedia

Orientationplus
Stabilizedplus
Make rs9268402(A;A)
Make rs9268402(A;G)
Make rs9268402(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32373576
GeneC6orf10
is asnp
is mentioned by
dbSNPrs9268402
ebirs9268402
HLIrs9268402
Exacrs9268402
Varsomers9268402
Maprs9268402
PheGenIrs9268402
hapmaprs9268402
1000 genomesrs9268402
hgdprs9268402
ensemblrs9268402
gopubmedrs9268402
geneviewrs9268402
scholarrs9268402
googlers9268402
pharmgkbrs9268402
gwascentralrs9268402
openSNPrs9268402
23andMers9268402
23andMe allrs9268402
SNP Nexus

SNPshotrs9268402
SNPdbers9268402
MSV3drs9268402
GWAS Ctlgrs9268402
GMAF0.4399
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22751097OA-icon.png]
Trait Coronary heart disease
Title Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Risk Allele G
P-val 3E-15
Odds Ratio 1.16 [1.12-1.20]


[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.


[PMID 26617759OA-icon.png] Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population.