DDX39B, DExD-box helicase 39B, 7919

N. diseases: 50; N. variants: 23
Disease: Graves Disease ×
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: rs2075580
rs2075580 		1.000 0.120 6 31536198 intron variant G/A;C snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs933208
rs933208 		1.000 0.120 6 31538871 synonymous variant G/T snv 0.76 0.76
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011