Have questions? Visit https://www.reddit.com/r/SNPedia

rs1689800

From SNPedia

Orientationminus
Stabilizedminus
Make rs1689800(C;C)
Make rs1689800(C;T)
Make rs1689800(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position182199750
is asnp
is mentioned by
dbSNPrs1689800
ebirs1689800
HLIrs1689800
Exacrs1689800
Varsomers1689800
Maprs1689800
PheGenIrs1689800
hapmaprs1689800
1000 genomesrs1689800
hgdprs1689800
ensemblrs1689800
gopubmedrs1689800
geneviewrs1689800
scholarrs1689800
googlers1689800
pharmgkbrs1689800
gwascentralrs1689800
openSNPrs1689800
23andMers1689800
23andMe allrs1689800
SNP Nexus

SNPshotrs1689800
SNPdbers1689800
MSV3drs1689800
GWAS Ctlgrs1689800
GMAF0.3053
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele G
P-val 3E-10
Odds Ratio 0.4700 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele G
P-val 5E-20
Odds Ratio .03 [NR] unit decrease