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rs2289360

From SNPedia

Orientationminus
Stabilizedminus
Make rs2289360(A;A)
Make rs2289360(A;G)
Make rs2289360(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27079297
GeneEMILIN1
is asnp
is mentioned by
dbSNPrs2289360
dbSNP (classic)rs2289360
ClinGenrs2289360
ebirs2289360
HLIrs2289360
Exacrs2289360
Gnomadrs2289360
Varsomers2289360
LitVarrs2289360
Maprs2289360
PheGenIrs2289360
Biobankrs2289360
1000 genomesrs2289360
hgdprs2289360
ensemblrs2289360
geneviewrs2289360
scholarrs2289360
googlers2289360
pharmgkbrs2289360
gwascentralrs2289360
openSNPrs2289360
23andMers2289360
SNPshotrs2289360
SNPdbers2289360
MSV3drs2289360
GWAS Ctlgrs2289360
GMAF0.404
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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


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