×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Breast Carcinoma
0.120
GeneticVariation
GWASCAT
Association analysis identifies 65 new breast cancer risk loci.
29059683
2017
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Alopecia
0.100
GeneticVariation
GWASCAT
Genetic prediction of male pattern baldness.
28196072
2017
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Blood urea nitrogen measurement
0.100
GeneticVariation
GWASCAT
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
31152163
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Blood urea nitrogen measurement
0.100
GeneticVariation
GWASCAT
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
29403010
2018
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Blood urea nitrogen measurement
0.100
GeneticVariation
GWASCAT
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
22797727
2012
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Red Blood Cell Count measurement
0.100
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Forced expiratory volume function
0.100
GeneticVariation
GWASCAT
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
30804560
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Other alopecia
0.100
GeneticVariation
GWASCAT
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
22693459
2012
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Other alopecia
0.100
GeneticVariation
GWASCAT
Detection and interpretation of shared genetic influences on 42 human traits.
27182965
2016
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Other alopecia
0.100
GeneticVariation
GWASCAT
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
29146897
2017
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Vital capacity
0.100
GeneticVariation
GWASCAT
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
30804560
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Androgenetic Alopecia
0.100
GeneticVariation
GWASCAT
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
29146897
2017
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Androgenetic Alopecia
0.100
GeneticVariation
GWASCAT
Detection and interpretation of shared genetic influences on 42 human traits.
27182965
2016
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Androgenetic Alopecia
0.100
GeneticVariation
GWASCAT
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
22693459
2012
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Uric acid measurement (procedure)
0.100
GeneticVariation
GWASCAT
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
21909109
2011
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Uric acid measurement (procedure)
0.100
GeneticVariation
GWASCAT
Genome-wide association study of hematological and biochemical traits in a Japanese population.
20139978
2010
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Adolescent idiopathic scoliosis
0.100
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Diastolic blood pressure
0.100
GeneticVariation
GWASCAT
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
30578418
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Systolic Pressure
0.100
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Systolic Pressure
0.100
GeneticVariation
GWASCAT
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
27841878
2017
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Body mass index
0.100
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Body mass index
0.100
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
30239722
2019
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Age at menarche
0.100
GeneticVariation
GWASCAT
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
21102462
2010
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
Mature B-Cell Neoplasm
0.100
GeneticVariation
GWASCAT
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.
25279986
2014
×
Entrez Id:
8170
Gene Symbol:
SLC14A2
SLC14A2
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.100
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018