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: rs11095197
rs11095197 		1.000 0.040 X 30958830 intron variant C/T snv 0.28
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs754992859
rs754992859 		1.000 0.040 X 30855520 missense variant C/T snv 5.7E-06
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.010 1.000 1 2016 2016