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rs13239907

From SNPedia

Orientationplus
Make rs13239907(A;A)
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Make rs13239907(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position74042520
GeneELN
is asnp
is mentioned by
dbSNPrs13239907
ebirs13239907
HLIrs13239907
Exacrs13239907
Varsomers13239907
Maprs13239907
PheGenIrs13239907
hapmaprs13239907
1000 genomesrs13239907
hgdprs13239907
ensemblrs13239907
gopubmedrs13239907
geneviewrs13239907
scholarrs13239907
googlers13239907
pharmgkbrs13239907
gwascentralrs13239907
openSNPrs13239907
23andMers13239907
23andMe allrs13239907
SNP Nexus

SNPshotrs13239907
SNPdbers13239907
MSV3drs13239907
GWAS Ctlgrs13239907
Max Magnitude
? (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