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rs2849165

From SNPedia

Orientationminus
Stabilizedminus
Make rs2849165(A;A)
Make rs2849165(A;G)
Make rs2849165(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position116817762
is asnp
is mentioned by
dbSNPrs2849165
dbSNP (old)rs2849165
ClinGenrs2849165
ebirs2849165
HLIrs2849165
Exacrs2849165
Varsomers2849165
Maprs2849165
PheGenIrs2849165
Biobankrs2849165
1000 genomesrs2849165
hgdprs2849165
ensemblrs2849165
gopubmedrs2849165
geneviewrs2849165
scholarrs2849165
googlers2849165
pharmgkbrs2849165
gwascentralrs2849165
openSNPrs2849165
23andMers2849165
23andMe allrs2849165
SNP Nexus

SNPshotrs2849165
SNPdbers2849165
MSV3drs2849165
GWAS Ctlgrs2849165
Max Magnitude

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

[PMID 28257648OA-icon.png] Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.