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rs1426391

From SNPedia

Orientationplus
Stabilizedplus
Make rs1426391(A;A)
Make rs1426391(A;C)
Make rs1426391(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position116072535
is asnp
is mentioned by
dbSNPrs1426391
ebirs1426391
HLIrs1426391
Exacrs1426391
Varsomers1426391
Maprs1426391
PheGenIrs1426391
hapmaprs1426391
1000 genomesrs1426391
hgdprs1426391
ensemblrs1426391
gopubmedrs1426391
geneviewrs1426391
scholarrs1426391
googlers1426391
pharmgkbrs1426391
gwascentralrs1426391
openSNPrs1426391
23andMers1426391
23andMe allrs1426391
SNP Nexus

SNPshotrs1426391
SNPdbers1426391
MSV3drs1426391
GWAS Ctlgrs1426391
GMAF0.3802
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23505323OA-icon.png]
Trait Hypertriglyceridemia
Title Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
Risk Allele
P-val 7E-6
Odds Ratio 1.25 [1.15-1.35]