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rs1558861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs1558861(C;C)
Make rs1558861(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116736721
is asnp
is mentioned by
dbSNPrs1558861
ebirs1558861
HLIrs1558861
Exacrs1558861
Varsomers1558861
Maprs1558861
PheGenIrs1558861
hapmaprs1558861
1000 genomesrs1558861
hgdprs1558861
ensemblrs1558861
gopubmedrs1558861
geneviewrs1558861
scholarrs1558861
googlers1558861
pharmgkbrs1558861
gwascentralrs1558861
openSNPrs1558861
23andMers1558861
23andMe allrs1558861
SNP Nexus

SNPshotrs1558861
SNPdbers1558861
MSV3drs1558861
GWAS Ctlgrs1558861
GMAF0.118
Max Magnitude0
GWAS
SNP rs1558861
PubMedID [PMID 18193046]
Condition Triglycerides
Gene LOC440069, MGC13125
Risk Allele A
pValue 2.00E-026
OR 17
95% CI 13.28-20.72) % highe



GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele T
P-val 0.000002
Odds Ratio 0.03 [0.02-0.04] unit decrease
? (C;C) (C;T) (T;T)


GET Evidence
rs1558861
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.929688
summary



[PMID 24402875] Genetic association of lipid metabolism related SNPs with myocardial infarction in the Pakistani population