NCL, nucleolin, 4691

N. diseases: 167; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16828074
rs16828074
Entrez Id: 4691
Gene Symbol: NCL
NCL
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASCAT Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. 23728934 2013
dbSNP: rs16828074
rs16828074
Entrez Id: 4691
Gene Symbol: NCL
NCL
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASDB Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. 23728934 2013
dbSNP: rs10202701
rs10202701
Entrez Id: 4691
Gene Symbol: NCL
NCL
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6737291
rs6737291
Entrez Id: 4691
Gene Symbol: NCL
NCL
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs7598759
rs7598759
Entrez Id: 4691;6082;654321
Gene Symbol: NCL;SNORD20;SNORA75
NCL;SNORD20;SNORA75
CUI: C0018781
Disease:
Noise-induced hearing loss 		0.700 GeneticVariation GWASCAT Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. 26121033 2015