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rs2304130

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2304130(A;G)
Make rs2304130(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position19678719
GeneZNF101
is asnp
is mentioned by
dbSNPrs2304130
ebirs2304130
HLIrs2304130
Exacrs2304130
Varsomers2304130
Maprs2304130
PheGenIrs2304130
hapmaprs2304130
1000 genomesrs2304130
hgdprs2304130
ensemblrs2304130
gopubmedrs2304130
geneviewrs2304130
scholarrs2304130
googlers2304130
pharmgkbrs2304130
gwascentralrs2304130
openSNPrs2304130
23andMers2304130
23andMe allrs2304130
SNP Nexus

SNPshotrs2304130
SNPdbers2304130
MSV3drs2304130
GWAS Ctlgrs2304130
GMAF0.1451
Max Magnitude0
? (A;A) (A;G) (G;G) 28
news three SNPs that appear to have different effects in men and women rs3846662 rs2304130 rs2083637
GWAS snp
PMID [PMID 19060911OA-icon.png]
Trait Cholesterol, total
Title Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Risk Allele G
P-val 2E-15
Odds Ratio 0.15 [NR] SD decrease


GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele G
P-val 4E-8
Odds Ratio 0.07 [0.04-0.10] unit decrease




[PMID 22359512OA-icon.png] Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations


[PMID 20832063] Exploring genetic determinants of plasma total cholesterol levels and their predictive value in a longitudinal study.


GET Evidence
rs2304130
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.115449
summary