|
rs9912530
|
LRRC37A2
|
Tonometry
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma.
|
29785010 |
2018 |
|
rs9896243
|
NSF;LRRC37A2
|
Anxiety
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
|
29942085 |
2018 |
|
rs9890413
|
WNT3;LRRC37A2
|
Cleft Lip with or without Cleft Palate
|
|
0.010 |
GeneticVariation |
BEFREE |
The rs9890413 variant marginally decreased the risk of nonsyndromic cleft lip with or without cleft palate in codominant (odds ratio = 0.41, 95% confidence interval = 0.17-0.99, P = 0.047, AG vs AA) model.
|
29356097 |
2018 |
|
rs916888
|
WNT3;LRRC37A2
|
Forced expiratory volume function
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
|
30061609 |
2018 |
|
rs916888
|
WNT3;LRRC37A2
|
Corpuscular Hemoglobin Concentration Mean
|
|
0.700 |
GeneticVariation |
GWASDB |
Seventy-five genetic loci influencing the human red blood cell.
|
23222517 |
2012 |
|
rs916888
|
WNT3;LRRC37A2
|
Vital capacity
|
|
0.700 |
GeneticVariation |
GWASCAT |
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
|
30061609 |
2018 |
|
rs916888
|
WNT3;LRRC37A2
|
Intelligence
|
|
0.700 |
GeneticVariation |
GWASCAT |
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
|
28093568 |
2017 |
|
rs916888
|
WNT3;LRRC37A2
|
Intelligence
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
|
29326435 |
2019 |
|
rs863223401
|
GOSR2;LRRC37A2
|
EPILEPSY, PROGRESSIVE MYOCLONIC, 6
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs8069437
|
WNT3;LRRC37A2
|
Hematocrit procedure
|
C |
0.700 |
GeneticVariation |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
rs8069437
|
WNT3;LRRC37A2
|
Blood Pressure
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|
21909110 |
2011 |
|
rs8069437
|
WNT3;LRRC37A2
|
Hemoglobin measurement
|
C |
0.700 |
GeneticVariation |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
rs8069437
|
WNT3;LRRC37A2
|
Red Blood Cell Count measurement
|
C |
0.700 |
GeneticVariation |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
|
rs786205887
|
WNT3;LRRC37A2
|
Bladder Exstrophy and Epispadias Complex
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs77819282
|
NSF;LRRC37A2;NSFP1
|
Thyroid stimulating hormone measurement
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
|
30367059 |
2018 |
|
rs76774446
|
GOSR2;LRRC37A2
|
Atrial Fibrillation
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Multi-ethnic genome-wide association study for atrial fibrillation.
|
29892015 |
2018 |
|
rs75230966
|
LRRC37A2
|
Systolic Pressure
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
|
rs7224296
|
NSF;LRRC37A2
|
Intelligence
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
|
29326435 |
2019 |
|
rs7224296
|
NSF;LRRC37A2
|
Parkinson Disease
|
|
0.700 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
|
rs7224296
|
NSF;LRRC37A2
|
Parkinson Disease
|
|
0.700 |
GeneticVariation |
GWASDB |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
|
21738487 |
2011 |
|
rs7224296
|
NSF;LRRC37A2
|
Corpuscular Hemoglobin Concentration Mean
|
|
0.700 |
GeneticVariation |
GWASDB |
Seventy-five genetic loci influencing the human red blood cell.
|
23222517 |
2012 |
|
rs7224296
|
NSF;LRRC37A2
|
Parkinson Disease
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|
19915575 |
2009 |
|
rs7224296
|
NSF;LRRC37A2
|
Progressive supranuclear palsy
|
|
0.010 |
GeneticVariation |
BEFREE |
Significant genetic overlap was also found between ALS and PSP at rs7224296, which tags the MAPT H1 haplotype (nearest gene, NSF; P = .045).
|
29630712 |
2018 |
|
rs7224296
|
NSF;LRRC37A2
|
Amyotrophic Lateral Sclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
Significant genetic overlap was also found between ALS and PSP at rs7224296, which tags the MAPT H1 haplotype (nearest gene, NSF; P = .045).
|
29630712 |
2018 |
|
rs7213526
|
GOSR2;LRRC37A2
|
Blood urea nitrogen measurement
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |