CDSN, corneodesmosin, 1041

N. diseases: 101; N. variants: 46
Disease: Behcet Syndrome ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3095324
rs3095324 		1.000 0.200 6 31119356 intron variant C/T snv 0.35
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs386579334
rs386579334 		1.000 0.200 6 31119356 intron variant C/T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.700 1.000 1 2012 2012