UBN1, ubinuclein 1, 29855

N. diseases: 11; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10500326
rs10500326
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1876359
rs1876359
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
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: rs8060576
rs8060576
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0205682
Disease:
Waist-Hip Ratio 		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: rs12446456
rs12446456
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs1395602
rs1395602
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0006826
Disease:
Malignant Neoplasms 		A 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs2251666
rs2251666
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0006826
Disease:
Malignant Neoplasms 		G 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs6500637
rs6500637
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0006826
Disease:
Malignant Neoplasms 		T 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs8064029
rs8064029
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0006826
Disease:
Malignant Neoplasms 		C 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148 2017
dbSNP: rs765004815
rs765004815
Entrez Id: 29855
Gene Symbol: UBN1
UBN1
CUI: C0455988
Disease:
Hydrops Fetalis, Non-Immune 		A 0.700 GeneticVariation CLINVAR Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families. 26036949 2015