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rs4963452

From SNPedia

Orientationplus
Stabilizedplus
Make rs4963452(C;C)
Make rs4963452(C;T)
Make rs4963452(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position62048331
is asnp
is mentioned by
dbSNPrs4963452
ebirs4963452
HLIrs4963452
Exacrs4963452
Varsomers4963452
Maprs4963452
PheGenIrs4963452
hapmaprs4963452
1000 genomesrs4963452
hgdprs4963452
ensemblrs4963452
gopubmedrs4963452
geneviewrs4963452
scholarrs4963452
googlers4963452
pharmgkbrs4963452
gwascentralrs4963452
openSNPrs4963452
23andMers4963452
23andMe allrs4963452
SNP Nexus

SNPshotrs4963452
SNPdbers4963452
MSV3drs4963452
GWAS Ctlgrs4963452
GMAF0.2479
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 6E-7
Odds Ratio 0.0200 [NR] % increase