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rs884843

From SNPedia

Orientationplus
Make rs884843(A;A)
Make rs884843(A;G)
Make rs884843(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position74031459
GeneELN
is asnp
is mentioned by
dbSNPrs884843
ebirs884843
HLIrs884843
Exacrs884843
Varsomers884843
Maprs884843
PheGenIrs884843
hapmaprs884843
1000 genomesrs884843
hgdprs884843
ensemblrs884843
gopubmedrs884843
geneviewrs884843
scholarrs884843
googlers884843
pharmgkbrs884843
gwascentralrs884843
openSNPrs884843
23andMers884843
23andMe allrs884843
SNP Nexus

SNPshotrs884843
SNPdbers884843
MSV3drs884843
GWAS Ctlgrs884843
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 25775011] The association of elastin gene variants with two angiographic subtypes of polypoidal choroidal vasculopathy