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rs2011616

From SNPedia

Orientationplus
Stabilizedplus
Make rs2011616(A;A)
Make rs2011616(A;G)
Make rs2011616(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27079693
GeneEMILIN1
is asnp
is mentioned by
dbSNPrs2011616
ebirs2011616
HLIrs2011616
Exacrs2011616
Varsomers2011616
Maprs2011616
PheGenIrs2011616
hapmaprs2011616
1000 genomesrs2011616
hgdprs2011616
ensemblrs2011616
gopubmedrs2011616
geneviewrs2011616
scholarrs2011616
googlers2011616
pharmgkbrs2011616
gwascentralrs2011616
openSNPrs2011616
23andMers2011616
23andMe allrs2011616
SNP Nexus

SNPshotrs2011616
SNPdbers2011616
MSV3drs2011616
GWAS Ctlgrs2011616
GMAF0.3462
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20186130] Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension


[PMID 22639547OA-icon.png] Pooled Analyses of the Associations of Polymorphisms in the GRK4 and EMILIN1 Genes with Hypertension Risk


[PMID 19922630OA-icon.png] Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population.


[PMID 21462127] [Association of EMILIN1 gene polymorphism with essential hypertension in Mongolian].


[PMID 21753788] Association of intronic single-nucleotide polymorphisms in the EMILIN1 gene with essential hypertension in a Chinese population.