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rs633389

From SNPedia

Orientationplus
Make rs633389(C;C)
Make rs633389(C;T)
Make rs633389(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position116796621
is asnp
is mentioned by
dbSNPrs633389
ebirs633389
HLIrs633389
Exacrs633389
Varsomers633389
Maprs633389
PheGenIrs633389
hapmaprs633389
1000 genomesrs633389
hgdprs633389
ensemblrs633389
gopubmedrs633389
geneviewrs633389
scholarrs633389
googlers633389
pharmgkbrs633389
gwascentralrs633389
openSNPrs633389
23andMers633389
23andMe allrs633389
SNP Nexus

SNPshotrs633389
SNPdbers633389
MSV3drs633389
GWAS Ctlgrs633389
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27257688] Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.