Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6731302
rs6731302
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0028754
Disease:
Obesity 		A 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs6731302
rs6731302
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0028754
Disease:
Obesity 		A 0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs2708146
rs2708146
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0040517
Disease:
Gilles de la Tourette syndrome 		A 0.710 GeneticVariation GWASCAT Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. 30818990 2019
dbSNP: rs2708146
rs2708146
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0040517
Disease:
Gilles de la Tourette syndrome 		0.710 GeneticVariation BEFREE Conditional FDR analysis further revealed novel variants significantly associated with TS (p < 8 × 10<sup>-7</sup>) when conditioning on intracranial (rs2708146, q = 0.046; and rs72853320, q = 0.035) and hippocampal (rs1922786, q = 0.001) volumes, respectively. 30902966 2019
dbSNP: rs10210385
rs10210385
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10210385
rs10210385
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs116219610
rs116219610
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0424574
Disease:
Duration of sleep 		T 0.700 GeneticVariation GWASCAT Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. 30804565 2019
dbSNP: rs13417036
rs13417036
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		A 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs1641155
rs1641155
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. 31453325 2019
dbSNP: rs17049502
rs17049502
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0205682
Disease:
Waist-Hip Ratio 		A 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: rs17049820
rs17049820
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0021704
Disease:
Intelligence 		T 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
dbSNP: rs1861412
rs1861412
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1305855
Disease:
Body mass index 		A 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: rs4671328
rs4671328
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
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: rs4671328
rs4671328
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62144560
rs62144560
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6731302
rs6731302
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs75539574
rs75539574
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0424574
Disease:
Duration of sleep 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698 2019
dbSNP: rs75539574
rs75539574
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0424574
Disease:
Duration of sleep 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698 2019
dbSNP: rs7573672
rs7573672
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs77732866
rs77732866
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs929641
rs929641
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0205682
Disease:
Waist-Hip Ratio 		A 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: rs10175478
rs10175478
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
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: rs10175478
rs10175478
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
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: rs17615494
rs17615494
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0392885
Disease:
High density lipoprotein measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs1861410
rs1861410
Entrez Id: 400955
Gene Symbol: LINC01122
LINC01122
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018