ADAMTSL3, ADAMTS like 3, 57188

N. diseases: 35; N. variants: 31
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs950169
rs950169
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs950169
rs950169
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
dbSNP: rs950169
rs950169
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs950169
rs950169
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061 2014
dbSNP: rs950169
rs950169
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0036341
Disease:
Schizophrenia 		0.800 GeneticVariation GWASDB A genome-wide investigation of SNPs and CNVs in schizophrenia. 19197363 2009
dbSNP: rs10152300
rs10152300
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		G 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs10906982
rs10906982
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs111470917
rs111470917
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs11259933
rs11259933
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11259936
rs11259936
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11630762
rs11630762
Entrez Id: 57188;105370935
Gene Symbol: ADAMTSL3;LOC105370935
ADAMTSL3;LOC105370935
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs118136305
rs118136305
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11856122
rs11856122
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0424621
Disease:
Body Fat Distribution 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs11856122
rs11856122
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0424621
Disease:
Body Fat Distribution 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs2135880
rs2135880
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2401171
rs2401171
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs4523894
rs4523894
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		C 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs4842838
rs4842838
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs7170165
rs7170165
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0035242
Disease:
Respiratory Tract Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7183263
rs7183263
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs8031704
rs8031704
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0518026
Disease:
body fat percentage (physical finding) 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs8038454
rs8038454
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs906427
rs906427
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7175718
rs7175718
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
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: rs7175718
rs7175718
Entrez Id: 57188
Gene Symbol: ADAMTSL3
ADAMTSL3
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