rs16996148
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs16996148(G;T) |
Make rs16996148(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 19547663 |
Gene | CILP2 |
is a | snp |
is | mentioned by |
dbSNP | rs16996148 |
dbSNP (classic) | rs16996148 |
ClinGen | rs16996148 |
ebi | rs16996148 |
HLI | rs16996148 |
Exac | rs16996148 |
Gnomad | rs16996148 |
Varsome | rs16996148 |
LitVar | rs16996148 |
Map | rs16996148 |
PheGenI | rs16996148 |
Biobank | rs16996148 |
1000 genomes | rs16996148 |
hgdp | rs16996148 |
ensembl | rs16996148 |
geneview | rs16996148 |
scholar | rs16996148 |
rs16996148 | |
pharmgkb | rs16996148 |
gwascentral | rs16996148 |
openSNP | rs16996148 |
23andMe | rs16996148 |
SNPshot | rs16996148 |
SNPdbe | rs16996148 |
MSV3d | rs16996148 |
GWAS Ctlg | rs16996148 |
GMAF | 0.101 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs16996148 |
PubMedID | [PMID 18193043] |
Condition | Triglycerides |
Gene | NCAN,CILP2 |
Risk Allele | G |
pValue | 3.00E-009 |
OR | 6.1 |
95% CI | NR) mg/dl highe |
GWAS snp | |
---|---|
PMID | [PMID 18193044] |
Trait | LDL cholesterol |
Title | Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans |
Risk Allele | G |
P-val | 2.9999999999999997E-8 |
Odds Ratio | 0.10 [0.06-0.14] % SD lower |
[PMID 21823004] Effects of SNPs at newly identified lipids loci on blood lipid levels and risk of coronary heart disease in Chinese Han population: A case control study
[PMID 18852197] Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
[PMID 18987386] Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population.
[PMID 19060910] Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
[PMID 19060911] Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
[PMID 19197348] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
[PMID 19435741] Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.
[PMID 19656773] A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.
[PMID 19951432] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.
[PMID 21691831] Triglyceride level-influencing functional variants of the ANGPTL3, CILP2, and TRIB1 loci in ischemic stroke.
[PMID 22208664] Sex-specific association of rs16996148 SNP in the NCAN/CILP2/PBX4 and serum lipid levels in the Mulao and Han populations.
[PMID 23098650] Impact of variants within seven candidate genes on statin treatment efficacy