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rs13046373

From SNPedia

Orientationplus
Stabilizedplus
Make rs13046373(A;A)
Make rs13046373(A;G)
Make rs13046373(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position30688172
is asnp
is mentioned by
dbSNPrs13046373
dbSNP (classic)rs13046373
ClinGenrs13046373
ebirs13046373
HLIrs13046373
Exacrs13046373
Gnomadrs13046373
Varsomers13046373
LitVarrs13046373
Maprs13046373
PheGenIrs13046373
Biobankrs13046373
1000 genomesrs13046373
hgdprs13046373
ensemblrs13046373
geneviewrs13046373
scholarrs13046373
googlers13046373
pharmgkbrs13046373
gwascentralrs13046373
openSNPrs13046373
23andMers13046373
SNPshotrs13046373
SNPdbers13046373
MSV3drs13046373
GWAS Ctlgrs13046373
GMAF0.4656
Max Magnitude0
? (A;A) (A;G) (G;G) 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 4E-6
Odds Ratio .02 [NR] unit decrease