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rs2366858

From SNPedia

Orientationplus
Stabilizedplus
Make rs2366858(A;A)
Make rs2366858(A;C)
Make rs2366858(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position80711306
is asnp
is mentioned by
dbSNPrs2366858
ebirs2366858
HLIrs2366858
Exacrs2366858
Varsomers2366858
Maprs2366858
PheGenIrs2366858
hapmaprs2366858
1000 genomesrs2366858
hgdprs2366858
ensemblrs2366858
gopubmedrs2366858
geneviewrs2366858
scholarrs2366858
googlers2366858
pharmgkbrs2366858
gwascentralrs2366858
openSNPrs2366858
23andMers2366858
23andMe allrs2366858
SNP Nexus

SNPshotrs2366858
SNPdbers2366858
MSV3drs2366858
GWAS Ctlgrs2366858
GMAF0.05785
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23726366OA-icon.png]
Trait HDL cholesterol
Title Genome-wide Characterization of Shared and Distinct Genetic Components that Influence Blood Lipid Levels in Ethnically Diverse Human Populations.
Risk Allele C
P-val 6E-10
Odds Ratio .03 [NR] unit increase