SNX20, sorting nexin 20, 124460

N. diseases: 4; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6596
rs6596
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0010346
Disease:
Crohn Disease
0.800 GeneticVariation GWASCAT Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. 28008999 2016
dbSNP: rs6596
rs6596
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0010346
Disease:
Crohn Disease
0.800 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
dbSNP: rs6596
rs6596
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.700 GeneticVariation GWASCAT Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. 28008999 2016
dbSNP: rs2270368
rs2270368
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0023343
Disease:
Leprosy
G 0.700 GeneticVariation GWASCAT Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy. 25642632 2015
dbSNP: rs2066848
rs2066848
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
dbSNP: rs2270368
rs2270368
Entrez Id: 124460
Gene Symbol: SNX20
SNX20
CUI: C0010346
Disease:
Crohn Disease
0.010 GeneticVariation BEFREE We identified 2 variants in the same genomic region (rs2270368 and rs17221417) that interact with smoking in relation to CD risk. 28506689 2017