Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1433210
rs1433210
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs143528679
rs143528679
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0001948
Disease:
Alcohol consumption 		G 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs143528679
rs143528679
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		G 0.700 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716 2019
dbSNP: rs3097937
rs3097937
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs4833941
rs4833941
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
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: rs4833941
rs4833941
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
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: rs62319742
rs62319742
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. 29455858 2018
dbSNP: rs7692299
rs7692299
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0008925
Disease:
Cleft Palate 		A 0.700 GeneticVariation GWASCAT Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. 28232668 2017
dbSNP: rs7692299
rs7692299
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0008924
Disease:
Cleft upper lip 		A 0.700 GeneticVariation GWASCAT Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. 28232668 2017
dbSNP: rs58530613
rs58530613
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0032181
Disease:
Platelet Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs111361850
rs111361850
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0004096
Disease:
Asthma 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma. 25918132 2015
dbSNP: rs3097940
rs3097940
Entrez Id: 285419
Gene Symbol: LINC01091
LINC01091
CUI: C0023343
Disease:
Leprosy 		0.700 GeneticVariation GWASDB Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy. 22019778 2011