rs1558162
POU6F2;LOC105375238
Metabolic Syndrome X
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
30621171
2019
rs1558162
POU6F2;LOC105375238
Bilirubin measurement
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
30621171
2019
rs2140910
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs2237403
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Body mass index
T
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
30239722
2019
rs3778934
POU6F2;POU6F2-AS1
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs3937443
POU6F2;LOC105375238
Metabolic Syndrome X
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
30621171
2019
rs3937443
POU6F2;LOC105375238
Bilirubin measurement
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
30621171
2019
rs4072719
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Vital capacity
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs58695218
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Smoking
A
0.700
GeneticVariation
GWASCAT
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
30643258
2019
rs952623
POU6F2;POU6F2-AS2
Intelligence
C
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
rs10268735
POU6F2;LOC105375239
mathematical ability
A
0.700
GeneticVariation
GWASCAT
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
30038396
2018
rs112503449
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
mathematical ability
A
0.700
GeneticVariation
GWASCAT
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
30038396
2018
rs12674371
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Tonometry
0.700
GeneticVariation
GWASCAT
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma.
30054594
2018
rs28599716
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Intelligence
0.700
GeneticVariation
GWASCAT
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
29844566
2018
rs62443626
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Intelligence
0.700
GeneticVariation
GWASCAT
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
29844566
2018
rs6952464
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Tonometry
C
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
rs60464047
×
Entrez Id:
11281
Gene Symbol:
POU6F2
POU6F2
Motion Sickness
T
0.700
GeneticVariation
GWASCAT
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
25628336
2015
rs121918261
POU6F2;LOC105375239
Wilms tumor and radial bilateral aplasia
T
0.700
CausalMutation
CLINVAR