rs2011616
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2011616(A;A) |
Make rs2011616(A;G) |
Make rs2011616(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 27079693 |
Gene | EMILIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs2011616 |
dbSNP (classic) | rs2011616 |
ClinGen | rs2011616 |
ebi | rs2011616 |
HLI | rs2011616 |
Exac | rs2011616 |
Gnomad | rs2011616 |
Varsome | rs2011616 |
LitVar | rs2011616 |
Map | rs2011616 |
PheGenI | rs2011616 |
Biobank | rs2011616 |
1000 genomes | rs2011616 |
hgdp | rs2011616 |
ensembl | rs2011616 |
geneview | rs2011616 |
scholar | rs2011616 |
rs2011616 | |
pharmgkb | rs2011616 |
gwascentral | rs2011616 |
openSNP | rs2011616 |
23andMe | rs2011616 |
SNPshot | rs2011616 |
SNPdbe | rs2011616 |
MSV3d | rs2011616 |
GWAS Ctlg | rs2011616 |
GMAF | 0.3462 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20186130] Association study of the elastin microfibril interfacer 1 (EMILIN1) gene in essential hypertension
[PMID 22639547] Pooled Analyses of the Associations of Polymorphisms in the GRK4 and EMILIN1 Genes with Hypertension Risk
[PMID 19922630] 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.