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rs9586179

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9586179(C;C)
Make rs9586179(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position103407737
is asnp
is mentioned by
dbSNPrs9586179
ebirs9586179
HLIrs9586179
Exacrs9586179
Varsomers9586179
Maprs9586179
PheGenIrs9586179
hapmaprs9586179
1000 genomesrs9586179
hgdprs9586179
ensemblrs9586179
gopubmedrs9586179
geneviewrs9586179
scholarrs9586179
googlers9586179
pharmgkbrs9586179
gwascentralrs9586179
openSNPrs9586179
23andMers9586179
23andMe allrs9586179
SNP Nexus

SNPshotrs9586179
SNPdbers9586179
MSV3drs9586179
GWAS Ctlgrs9586179
GMAF0.186
Max Magnitude0
? (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 4E-7
Odds Ratio 0.0500 [NR] % increase