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rs3798713

From SNPedia

Orientationplus
Stabilizedplus
Make rs3798713(C;C)
Make rs3798713(C;G)
Make rs3798713(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position11008389
GeneELOVL2
is asnp
is mentioned by
dbSNPrs3798713
ebirs3798713
HLIrs3798713
Exacrs3798713
Varsomers3798713
Maprs3798713
PheGenIrs3798713
hapmaprs3798713
1000 genomesrs3798713
hgdprs3798713
ensemblrs3798713
gopubmedrs3798713
geneviewrs3798713
scholarrs3798713
googlers3798713
pharmgkbrs3798713
gwascentralrs3798713
openSNPrs3798713
23andMers3798713
23andMe allrs3798713
SNP Nexus

SNPshotrs3798713
SNPdbers3798713
MSV3drs3798713
GWAS Ctlgrs3798713
GMAF0.4936
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21829377OA-icon.png]
Trait
Title Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium.
Risk Allele C
P-val 2E-12
Odds Ratio 0.0400 [NR] % increase