GWAS snp
|
PMID
|
[PMID 20935630 ]
|
Trait
|
|
Title
|
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
|
Risk Allele
|
T
|
P-val
|
2E-13
|
Odds Ratio
|
0.19 [0.11-0.27] kg/m2 increase
|
GWAS snp
|
PMID
|
[PMID 21909115 ]
|
Trait
|
|
Title
|
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
Risk Allele
|
T
|
P-val
|
2E-17
|
Odds Ratio
|
0.6840 [NR] mmHg decrease
|
GWAS snp
|
PMID
|
[PMID 21909110 ]
|
Trait
|
|
Title
|
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|
Risk Allele
|
T
|
P-val
|
1E-10
|
Odds Ratio
|
0.6330 [0.44-0.82] mmHg decrease
|
GWAS snp
|
PMID
|
[PMID 20686565 ]
|
Trait
|
|
Title
|
Biological, clinical and population relevance of 95 loci for blood lipids.
|
Risk Allele
|
T
|
P-val
|
7E-11
|
Odds Ratio
|
0.8400 None
|
[PMID 19503599
] The impact of divergence time on the nature of population structure: an example from Iceland.
[PMID 22078303] Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia.
[PMID 23471855
] The genetics of childhood obesity and interaction with dietary macronutrients.
GWAS snp
|
PMID
|
[PMID 24097068 ]
|
Trait
|
HDL cholesterol
|
Title
|
Discovery and refinement of loci associated with lipid levels.
|
Risk Allele
|
T
|
P-val
|
1E-15
|
Odds Ratio
|
.07 [NR] unit decrease
|
[PMID 26006263
] Recent Positive Selection Drives the Expansion of a Schizophrenia Risk Nonsynonymous Variant at SLC39A8 in Europeans
[PMID 25184405] Subclinical psychotic experiences in healthy young adults: associations with stress and genetic predisposition
[PMID 26908625] Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.
[PMID 27492617
] A pleiotropic missense variant in SLC39A8 is associated with Crohn's disease and human gut microbiome composition.
[PMID 31533672
] SLC39A8 is a risk factor for schizophrenia in Uygur Chinese: a case-control study.
[PMID 31998841
] Functional validity, role, and implications of heavy alcohol consumption genetic loci.
[PMID 32897876
] Pleiotropic ZIP8 A391T implicates abnormal manganese homeostasis in complex human disease.
[PMID 32788640
] Genetic markers and continuity of healthy metabolic status: Tehran cardio-metabolic genetic study (TCGS).