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rs7016880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs7016880(C;C)
Make rs7016880(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position20019235
is asnp
is mentioned by
dbSNPrs7016880
ebirs7016880
HLIrs7016880
Exacrs7016880
Varsomers7016880
Maprs7016880
PheGenIrs7016880
hapmaprs7016880
1000 genomesrs7016880
hgdprs7016880
ensemblrs7016880
gopubmedrs7016880
geneviewrs7016880
scholarrs7016880
googlers7016880
pharmgkbrs7016880
gwascentralrs7016880
openSNPrs7016880
23andMers7016880
23andMe allrs7016880
SNP Nexus

SNPshotrs7016880
SNPdbers7016880
MSV3drs7016880
GWAS Ctlgrs7016880
GMAF0.09412
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20657596OA-icon.png]
Trait Hypertriglyceridemia
Title Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Risk Allele
P-val 2E-7
Odds Ratio 3.13 [2.04-4.76]