CDSN, corneodesmosin, 1041

N. diseases: 101; N. variants: 46
Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3095324
rs3095324
Entrez Id: 1041;170679
Gene Symbol: CDSN;PSORS1C1
CDSN;PSORS1C1
CUI: C0004943
Disease:
Behcet Syndrome 		0.700 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
dbSNP: rs386579334
rs386579334
Entrez Id: 1041;170679
Gene Symbol: CDSN;PSORS1C1
CDSN;PSORS1C1
CUI: C0004943
Disease:
Behcet Syndrome 		0.700 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012