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: rs7623687
rs7623687 		1.000 0.040 3 49411133 intron variant A/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 3 2017 2018
dbSNP: rs6784820
rs6784820 		1.000 0.040 3 49413431 intron variant A/G snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2008 2008
dbSNP: rs6997
rs6997 		1.000 0.040 3 49416401 3 prime UTR variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2007 2007