Rs4404477

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Orientationminus
Make rs4404477(A;A)
Make rs4404477(A;G)
Make rs4404477(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position117655921
GeneLSAMP
is asnp
is mentioned by
dbSNPrs4404477
PheGenIrs4404477
nextbiors4404477
hapmaprs4404477
1000 genomesrs4404477
hgdprs4404477
ensemblrs4404477
gopubmedrs4404477
geneviewrs4404477
scholarrs4404477
googlers4404477
pharmgkbrs4404477
gwascentralrs4404477
openSNPrs4404477
23andMers4404477
23andMe allrs4404477
SNP Nexus

SNPshotrs4404477
SNPdbers4404477
MSV3drs4404477
GMAF0.27
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18318786OA-icon.png],AEHA 2008 ppt - rs4404477(A)/rs1676232(A) defines a significant left main coronary artery disease risk haplotype