N4BP2L2, NEDD4 binding protein 2 like 2, 10443

N. diseases: 13; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2239748
rs2239748
Entrez Id: 10443
Gene Symbol: N4BP2L2
N4BP2L2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs743760
rs743760
Entrez Id: 10443;100462953
Gene Symbol: N4BP2L2;MICOS10P1
N4BP2L2;MICOS10P1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs703212
rs703212
Entrez Id: 10443
Gene Symbol: N4BP2L2
N4BP2L2
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs9591012
rs9591012
Entrez Id: 10443
Gene Symbol: N4BP2L2
N4BP2L2
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs1158061584
rs1158061584
Entrez Id: 10443
Gene Symbol: N4BP2L2
N4BP2L2
CUI: C0349588
Disease:
Short stature 		AT 0.700 CausalMutation CLINVAR