SLC14A2, solute carrier family 14 member 2, 8170

N. diseases: 71; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8085664
rs8085664
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C4083212
Disease:
Alopecia, Male Pattern 		C 0.800 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017
dbSNP: rs10502861
rs10502861
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C4083212
Disease:
Alopecia, Male Pattern 		C 0.800 GeneticVariation GWASCAT Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
dbSNP: rs10502861
rs10502861
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C4083212
Disease:
Alopecia, Male Pattern 		C 0.800 GeneticVariation GWASDB Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
dbSNP: rs7227483
rs7227483
Entrez Id: 8170;107985153
Gene Symbol: SLC14A2;LOC107985153
SLC14A2;LOC107985153
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		G 0.800 GeneticVariation GWASCAT Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. 22797727 2012
dbSNP: rs7227483
rs7227483
Entrez Id: 8170;107985153
Gene Symbol: SLC14A2;LOC107985153
SLC14A2;LOC107985153
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		G 0.800 GeneticVariation GWASDB Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. 22797727 2012
dbSNP: rs8085664
rs8085664
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C4083212
Disease:
Alopecia, Male Pattern 		0.800 GeneticVariation GWASDB Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. 22693459 2012
dbSNP: rs2243803
rs2243803
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C1314691
Disease:
Age at menarche 		A 0.800 GeneticVariation GWASDB Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs2243803
rs2243803
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C1314691
Disease:
Age at menarche 		A 0.800 GeneticVariation GWASCAT Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 21102462 2010
dbSNP: rs10438964
rs10438964
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1484873
rs1484873
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs16978350
rs16978350
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C1305855
Disease:
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
dbSNP: rs2543029
rs2543029
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs2705366
rs2705366
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7236548
rs7236548
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8090126
rs8090126
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs8093563
rs8093563
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9807668
rs9807668
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs9807668
rs9807668
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0042834
Disease:
Vital capacity 		T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs2612539
rs2612539
Entrez Id: 8170;101927980
Gene Symbol: SLC14A2;SLC14A2-AS1
SLC14A2;SLC14A2-AS1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 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
dbSNP: rs2612539
rs2612539
Entrez Id: 8170;101927980
Gene Symbol: SLC14A2;SLC14A2-AS1
SLC14A2;SLC14A2-AS1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 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
dbSNP: rs4890293
rs4890293
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0005845
Disease:
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
dbSNP: rs10502861
rs10502861
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0002170
Disease:
Alopecia 		T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs2193635
rs2193635
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs34800162
rs34800162
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C0002170
Disease:
Alopecia 		G 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs8085664
rs8085664
Entrez Id: 8170
Gene Symbol: SLC14A2
SLC14A2
CUI: C2678038
Disease:
Alopecia, Androgenetic, 2 		C 0.700 GeneticVariation GWASCAT GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. 29146897 2017