Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142529006
rs142529006
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
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: rs142529006
rs142529006
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs142529006
rs142529006
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs142529006
rs142529006
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1963304
rs1963304
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2897075
rs2897075
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
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: rs1015538
rs1015538
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs6963345
rs6963345
Entrez Id: 7586
Gene Symbol: ZKSCAN1
ZKSCAN1
CUI: C0206062
Disease:
Lung Diseases, Interstitial 		A 0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980 2013