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rs12967135

From SNPedia

Orientationplus
Stabilizedplus
Make rs12967135(A;A)
Make rs12967135(A;G)
Make rs12967135(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position60181790
is asnp
is mentioned by
dbSNPrs12967135
dbSNP (classic)rs12967135
ClinGenrs12967135
ebirs12967135
HLIrs12967135
Exacrs12967135
Gnomadrs12967135
Varsomers12967135
LitVarrs12967135
Maprs12967135
PheGenIrs12967135
Biobankrs12967135
1000 genomesrs12967135
hgdprs12967135
ensemblrs12967135
geneviewrs12967135
scholarrs12967135
googlers12967135
pharmgkbrs12967135
gwascentralrs12967135
openSNPrs12967135
23andMers12967135
SNPshotrs12967135
SNPdbers12967135
MSV3drs12967135
GWAS Ctlgrs12967135
GMAF0.2222
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele A
P-val 7E-9
Odds Ratio 0.4200 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele A
P-val 4E-8
Odds Ratio .03 [NR] unit decrease