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rs2856728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2856728(C;T)
Make rs2856728(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position74056452
GeneELN
is asnp
is mentioned by
dbSNPrs2856728
ebirs2856728
HLIrs2856728
Exacrs2856728
Varsomers2856728
Maprs2856728
PheGenIrs2856728
hapmaprs2856728
1000 genomesrs2856728
hgdprs2856728
ensemblrs2856728
gopubmedrs2856728
geneviewrs2856728
scholarrs2856728
googlers2856728
pharmgkbrs2856728
gwascentralrs2856728
openSNPrs2856728
23andMers2856728
23andMe allrs2856728
SNP Nexus

SNPshotrs2856728
SNPdbers2856728
MSV3drs2856728
GWAS Ctlgrs2856728
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 23294012] Association of polymorphisms in the elastin gene with sporadic ruptured intracranial aneurysms and unruptured intracranial aneurysms in Chinese patients


[PMID 25775011OA-icon.png] The association of elastin gene variants with two angiographic subtypes of polypoidal choroidal vasculopathy


ClinVar
Risk rs2856728(T;T)
Alt rs2856728(T;T)
Reference rs2856728(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ELN
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.73470782C>T
CLNSRC
CLNACC RCV000200638.1,