Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs947583
rs947583
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0202178
Disease:
Phosphorus measurement 		C 0.800 GeneticVariation GWASCAT Common genetic variants associate with serum phosphorus concentration. 20558539 2010
dbSNP: rs947583
rs947583
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0523827
Disease:
Inorganic phosphate measurement 		C 0.800 GeneticVariation GWASDB Common genetic variants associate with serum phosphorus concentration. 20558539 2010
dbSNP: rs947583
rs947583
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0523827
Disease:
Inorganic phosphate measurement 		C 0.800 GeneticVariation GWASCAT Common genetic variants associate with serum phosphorus concentration. 20558539 2010
dbSNP: rs947583
rs947583
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0202178
Disease:
Phosphorus measurement 		C 0.800 GeneticVariation GWASDB Common genetic variants associate with serum phosphorus concentration. 20558539 2010
dbSNP: rs9494266
rs9494266
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 GeneticVariation BEFREE Data from large samples of Danish individuals do not support a role for AHI1 rs1535435 nor rs9494266 as major type 2 diabetes variants. 18227995 2008
dbSNP: rs9494266
rs9494266
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 GeneticVariation GWASDB Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. 17668382 2007
dbSNP: rs116990752
rs116990752
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs144124553
rs144124553
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2327650
rs2327650
Entrez Id: 100131814;105378013
Gene Symbol: LINC00271;LOC105378013
LINC00271;LOC105378013
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4895455
rs4895455
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs761357
rs761357
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs761357
rs761357
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs761357
rs761357
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs761357
rs761357
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs761357
rs761357
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs79846291
rs79846291
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0002395
Disease:
Alzheimer's Disease 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. 29274321 2018
dbSNP: rs9389316
rs9389316
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C2699541
Disease:
Cytokine Measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502 2012
dbSNP: rs9647635
rs9647635
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE The case-control analysis did not show any difference in the genotypic distribution of the SNPs, while in the allelic analysis, a weak association was found between the rs9647635 A allele and SCZ. 25622261 2015
dbSNP: rs7750586
rs7750586
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Particularly, rs7750586 and rs911507, both located upstream of the AHI1 coding region, were found to be associated with schizophrenia in the analysis of genotypic (p = 0.0033, and 0.031, respectively) and allelic frequencies (p = 0.001 in both cases). 20805890 2010
dbSNP: rs911507
rs911507
Entrez Id: 100131814
Gene Symbol: LINC00271
LINC00271
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Particularly, rs7750586 and rs911507, both located upstream of the AHI1 coding region, were found to be associated with schizophrenia in the analysis of genotypic (p = 0.0033, and 0.031, respectively) and allelic frequencies (p = 0.001 in both cases). 20805890 2010