rs10853087
|
GOSR2;LRRC37A2
|
Blood urea nitrogen measurement
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
|
29403010 |
2018 |
rs141554661
|
GOSR2;LRRC37A2
|
Seizures
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs141554661
|
GOSR2;LRRC37A2
|
Myoclonic Epilepsies, Progressive
|
A |
0.700 |
GeneticVariation |
CLINVAR |
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.
|
21549339 |
2011 |
rs141554661
|
GOSR2;LRRC37A2
|
EPILEPSY, PROGRESSIVE MYOCLONIC, 6
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1568177307
|
GOSR2;LRRC37A2
|
Myoclonic Epilepsies, Progressive
|
G |
0.700 |
GeneticVariation |
CLINVAR |
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia.
|
21549339 |
2011 |
rs16941382
|
GOSR2;LRRC37A2
|
Coronary Arteriosclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
The G-T haplotype established by rs3785889-rs16941382 may be a risk genetic marker for coronary artery disease patients in Chinese Han population.
|
29137253 |
2017 |
rs16941382
|
GOSR2;LRRC37A2
|
Coronary heart disease
|
|
0.010 |
GeneticVariation |
BEFREE |
The G-T haplotype established by rs3785889-rs16941382 may be a risk genetic marker for coronary artery disease patients in Chinese Han population.
|
29137253 |
2017 |
rs16941382
|
GOSR2;LRRC37A2
|
Coronary Artery Disease
|
|
0.010 |
GeneticVariation |
BEFREE |
The G-T haplotype established by rs3785889-rs16941382 may be a risk genetic marker for coronary artery disease patients in Chinese Han population.
|
29137253 |
2017 |
rs17608766
|
GOSR2;LRRC37A2
|
Heart Function Tests
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
|
21076409 |
2010 |
rs17608766
|
GOSR2;LRRC37A2
|
Heart Function Tests
|
C |
0.800 |
GeneticVariation |
GWASDB |
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
|
21076409 |
2010 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs17608766
|
GOSR2;LRRC37A2
|
Mean blood pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|
21909110 |
2011 |
rs17608766
|
GOSR2;LRRC37A2
|
Cardiovascular Diseases
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs17608766
|
GOSR2;LRRC37A2
|
Coronary Artery Disease
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
rs17608766
|
GOSR2;LRRC37A2
|
Mean blood pressure
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
|
27618448 |
2016 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
|
27618452 |
2016 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic blood pressure measurement
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
21909115 |
2011 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
|
28739976 |
2017 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
|
27618447 |
2016 |
rs17608766
|
GOSR2;LRRC37A2
|
Systolic Pressure
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
|
30578418 |
2019 |
rs17608766
|
GOSR2;LRRC37A2
|
Blood Pressure
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|
21909110 |
2011 |
rs17608766
|
GOSR2;LRRC37A2
|
QRS complex feature
|
|
0.700 |
GeneticVariation |
GWASCAT |
52 Genetic Loci Influencing Myocardial Mass.
|
27659466 |
2016 |
rs1838105
|
GOSR2;LRRC37A2
|
Cleft upper lip
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
|
28232668 |
2017 |