rs12670798
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12670798(C;C) |
Make rs12670798(C;T) |
Make rs12670798(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 21567734 |
Gene | DNAH11, LOC105375183 |
is a | snp |
is | mentioned by |
dbSNP | rs12670798 |
dbSNP (classic) | rs12670798 |
ClinGen | rs12670798 |
ebi | rs12670798 |
HLI | rs12670798 |
Exac | rs12670798 |
Gnomad | rs12670798 |
Varsome | rs12670798 |
LitVar | rs12670798 |
Map | rs12670798 |
PheGenI | rs12670798 |
Biobank | rs12670798 |
1000 genomes | rs12670798 |
hgdp | rs12670798 |
ensembl | rs12670798 |
geneview | rs12670798 |
scholar | rs12670798 |
rs12670798 | |
pharmgkb | rs12670798 |
gwascentral | rs12670798 |
openSNP | rs12670798 |
23andMe | rs12670798 |
SNPshot | rs12670798 |
SNPdbe | rs12670798 |
MSV3d | rs12670798 |
GWAS Ctlg | rs12670798 |
GMAF | 0.3081 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
per the 23andMe blog, the minor allele of this SNP (C) was associated with increased cholesterol and triglycerides
SNP | Rarer allele | LDL | HDL | TG |
---|---|---|---|---|
rs6544713 | T | + | ||
rs2650000 | A | + | ||
rs471364 | C | - | ||
rs1800961 | T | - | ||
rs7679 | C | - | + | |
rs2967605 | T | - | ||
rs2409722 | T | - | ||
rs10903129 | A | - | - | - |
rs6756629 | A | - | + | - |
rs12670798 | C | + | + | + |
rs7395662 | A | - | + | + |
rs174570 | T | - | - | + |
rs2271293 | A | - | + | - |
rs2624265 | C | + | ||
rs2167079 | T | + | ||
rs9891572 | T | + | ||
rs4844614 | T | + | ||
rs5031002 | G | + |
GWAS snp | |
---|---|
PMID | [PMID 19060911] |
Trait | Cholesterol, total |
Title | Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts |
Risk Allele | G |
P-val | 9E-7 |
Odds Ratio | 0.06 [NR] SD increase |
GWAS snp | |
---|---|
PMID | [PMID 20686565] |
Trait | |
Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
Risk Allele | T |
P-val | 7E-10 |
Odds Ratio | 1.7000 None |
[PMID 19951432] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.
[PMID 20502693] Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.
GWAS snp | |
---|---|
PMID | [PMID 24097068] |
Trait | Cholesterol, total |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | C |
P-val | 1E-16 |
Odds Ratio | .04 [NR] unit increase |