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rs11902417

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Orientationplus
Stabilizedplus
Make rs11902417(A;A)
Make rs11902417(A;G)
Make rs11902417(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position20976028
is asnp
is mentioned by
dbSNPrs11902417
ebirs11902417
HLIrs11902417
Exacrs11902417
Varsomers11902417
Maprs11902417
PheGenIrs11902417
hapmaprs11902417
1000 genomesrs11902417
hgdprs11902417
ensemblrs11902417
gopubmedrs11902417
geneviewrs11902417
scholarrs11902417
googlers11902417
pharmgkbrs11902417
gwascentralrs11902417
openSNPrs11902417
23andMers11902417
23andMe allrs11902417
SNP Nexus

SNPshotrs11902417
SNPdbers11902417
MSV3drs11902417
GWAS Ctlgrs11902417
GMAF0.3535
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele G
P-val 4E-7
Odds Ratio 0.02 [0.01-0.03] unit decrease