Have questions? Visit https://www.reddit.com/r/SNPedia

rs884843

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs884843
ClinGenrs884843
ebirs884843
HLIrs884843
Exacrs884843
Gnomadrs884843
Varsomers884843
LitVarrs884843
Maprs884843
PheGenIrs884843
Biobankrs884843
1000 genomesrs884843
hgdprs884843
ensemblrs884843
geneviewrs884843
scholarrs884843
googlers884843
pharmgkbrs884843
gwascentralrs884843
openSNPrs884843
23andMers884843
SNPshotrs884843
SNPdbers884843
MSV3drs884843
GWAS Ctlgrs884843
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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